Annotations.csv

,doi,type,text_redacted
0,10.1016/j.jpcs.2012.04.017,solid_state_ceramic_synthesis,Analytical reagent grade powders (purity 99.5%) of ... cooled to room temperature along with the furnace.
1,10.1016/j.jeurceramsoc.2016.03.005,solid_state_ceramic_synthesis,A conventional solid-state reaction method was use ...  enriched atmosphere of the respective components.
2,10.1007/s10854-017-6447-z,solid_state_ceramic_synthesis,The Ni-doped 0.9Pb(Mg1/3Nb2/3)O3-0.1PbTiO3 (PMN-0. ... PT powders inside the crucible as packing powders.
3,10.1016/j.matchemphys.2009.03.003,solid_state_ceramic_synthesis,The (x) CoFe2O4 + (1 - x) Ba0.8Sr0.2TiO3 (where x  ... ere finally sintered at 1150 degC for 12 h in air.
4,10.1016/j.jallcom.2008.02.022,solid_state_ceramic_synthesis,Analytical reagent grade powders (purity 99.5%) of ... cooled to the room temperature along with furnace.
5,10.1007/s10854-012-0996-y,solid_state_ceramic_synthesis,BF-BT ceramics with excess Bi2O3 were prepared wit ... one oil at 80-100 degC under 3-5 kV/mm for 10 min.
6,10.1007/s10854-011-0614-4,solid_state_ceramic_synthesis,"Zn1-xCoxO (x = 0.01, 0.05 and 0.1) bulk ceramics w ... um atmosphere after the sintering period finished."
7,10.1016/j.jpcs.2009.03.004,solid_state_ceramic_synthesis,Analytical reagent grade powders (purity 99.5%) of ... samples were naturally cooled to room temperature.
8,10.1007/s10854-007-9492-1,solid_state_ceramic_synthesis,PLSZFT ceramics were prepared by solid state react ... es were cooled to the room temperature in furnace.
9,10.1016/j.jeurceramsoc.2011.08.036,solid_state_ceramic_synthesis,Specimens of the ZnLi2/3Ti4/3O4 ceramic were prepa ...  pellets were sintered at 900 degC for 2 h in air.
10,10.1016/j.matchemphys.2005.06.015,solid_state_ceramic_synthesis,"Undoped and La2O3 doped (0.5, 1.0, 2.0, 3.0 wt.%)  ... r paint for low frequency electrical measurements."
11,10.1016/j.jallcom.2014.10.045,solid_state_ceramic_synthesis,The ceramics with the composition of K0.5Na0.5Nb0. ... pplying a DC electric field of 3 kV/mm for 30 min.
12,10.1111/j.1551-2916.2010.03690.x,solid_state_ceramic_synthesis,"(Mg1-xNix)Al2O4 ceramics, where x=0-1, were synthe ... gC in air for 3 h at a heating rate of 10degC/min."
13,10.1007/s10854-012-0798-2,solid_state_ceramic_synthesis,Samples of general composition NdxSr1-xTiO3 (herea ... electric properties with as-sintered counterparts.
14,10.1016/j.jmmm.2015.10.051,solid_state_ceramic_synthesis,Various polycrystalline (1-y)BDFO-yNZFO composites ...  870 degC for 4 h and ready for characterizations.
15,10.1016/j.materresbull.2012.06.035,solid_state_ceramic_synthesis,"BZT ceramics doped with Nb2O5, MnO2 or V2O3 were p ... tered at 1400, 1500 or 1600 degC, for 2 h, in air."
16,10.1016/j.matlet.2016.03.089,solid_state_ceramic_synthesis,A conventional solid-state reaction method was use ... ey were then sintered in air at 1180 degC for 2 h.
17,10.1007/s10854-011-0610-8,solid_state_ceramic_synthesis,Specimens of the BTMNN-x ceramics were prepared th ... 2 h with a heating and cooling rate of 5 degC/min.
18,10.1111/j.1744-7402.2009.02380.x,solid_state_ceramic_synthesis,"KNLNS-x (x=0-10 mol%) lead-free piezoelectric cera ... eratures, in the range between 30degC and 150degC."
19,10.1007/s10854-010-0203-y,solid_state_ceramic_synthesis,Conventional solid state ceramic route was used to ... ples were then furnace cooled to room temperature.
20,10.1016/j.mseb.2011.12.015,solid_state_ceramic_synthesis,The chosen composition was Pb0.99[(Zr0.90Sn0.10)0. ...  temperature was then lowered to room temperature.
21,10.1016/j.matlet.2004.04.005,solid_state_ceramic_synthesis,(Pb0.48Ca0.52)(Fe0.5Nb0.5)O3 including xmol% CeO2  ... and PbZrO3+ZrO2 (10 wt.%) powders surrounded them.
22,10.1016/j.matlet.2015.11.046,solid_state_ceramic_synthesis,Li2Mg3TiO6 ceramics were prepared by a conventiona ... s in order to prevent the evaporation of Li and F.
23,10.1016/j.jallcom.2008.06.011,solid_state_ceramic_synthesis,Y-type hexagonal ferrite samples comprising Ba2Zn0 ... egC for 4 h in air and then cooled in the furnace.
24,10.1007/s10854-013-1665-5,solid_state_ceramic_synthesis,"Ca3-xNdxCo4Oy polycrystalline ceramic materials, w ... at 910 degC for 24 h with a final furnace cooling."
25,10.1007/s10853-013-7355-0,solid_state_ceramic_synthesis,(K0.455Na0.5Li0.045)(Nb0.9Ta0.1)O3 powders were sy ... er and balls was always maintained during milling.
26,10.1016/j.matchemphys.2013.06.010,solid_state_ceramic_synthesis,"The Li2Zn(1-x)NixTi3O8 (x = 0, 0.1, 0.2, 0.4 and 1 ... temperature was optimized for higher bulk density."
27,10.1007/s10854-014-2469-y,solid_state_ceramic_synthesis,The Ca3Co4-xTixO9 polycrystalline ceramic material ... at 910 degC for 24 h with a final furnace cooling.
28,10.1016/j.matchemphys.2012.09.004,solid_state_ceramic_synthesis,Specimens of the MgLi2/3Ti4/3O4 ceramic were prepa ... order to reduce the volatilization of Li elements.
29,10.1007/s10853-008-3142-8,solid_state_ceramic_synthesis,0.45TiO2-0.55CeTe2O6 and xZrTe3O8-(1 - x)CeTe2O6 p ... ent atmosphere at temperatures at around 700 degC.
30,10.1016/j.jpowsour.2008.09.068,solid_state_ceramic_synthesis,La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM) and La0.8Sr0.2Ga0. ... ty) and then sintered at 1500 degC for 6 h in air.
31,10.1007/s11665-013-0569-0,solid_state_ceramic_synthesis,The nanocrystalline BaTiO3 powder has been obtaine ...  wheel every 6 min after a rest interval of 2 min.
32,10.1016/j.mseb.2010.06.018,solid_state_ceramic_synthesis,"xZnWO4-(1 - x)Ba0.5Sr0.5TiO3 (BST) (x = 0.0, 5.0,  ... wed by sintering at 1200-1240 degC in air for 4 h."
33,10.1016/j.jallcom.2015.01.259,solid_state_ceramic_synthesis,"Polycrystalline single phase Bi4-xSmxTi3-xFexO12+- ... e of 5 degC min-1, with cooling in air atmosphere."
34,10.1016/j.ssc.2015.01.004,solid_state_ceramic_synthesis,Ceramics powers conforming to the chemical formula ...  embedded in the powder with the same composition.
35,10.1007/s10854-008-9721-2,solid_state_ceramic_synthesis,Specimens of the LNT ceramics were prepared by a c ... 2.0 wt% BCu and then sintered at 900 degC for 2 h.
36,10.1016/j.matlet.2006.01.062,solid_state_ceramic_synthesis,The raw materials used were commercially available ... ) in order to investigate the formation of PbTiO3.
37,10.1007/s10854-016-5382-8,solid_state_ceramic_synthesis,"(Ba0.92Bi0.08)(Ti0.92Fe0.08)O3 ceramics, abbreviat ... he PVA, then sintered at 1250 degC for 3 h in air."
38,10.1007/s10854-014-2275-6,solid_state_ceramic_synthesis,Ca1-x(La0.5Na0.5)xWO4 powders with compositions of ... ent atmosphere at temperature of 850 degC for 2 h.
39,10.1016/j.jeurceramsoc.2015.10.019,solid_state_ceramic_synthesis,The (1-x)NBT-xST ceramics were prepared using a co ...  of the discs and annealed at 500 degC for 30 min.
40,10.1016/j.jeurceramsoc.2010.10.033,solid_state_ceramic_synthesis,Na0.5K0.5NbO3 (NKN) and Na0.475K0.475Li0.05NbO3 (N ... finally cooling to room temperature at 180 degC/h.
41,10.1007/s10854-006-9094-3,solid_state_ceramic_synthesis,"Undoped and MnCO3 doped (0.3, 0.5, 1, 2mol%) Ba0.5 ... 50 degC for 3 h, depending on the amount of MnCO3."
42,10.1007/s10853-011-5650-1,solid_state_ceramic_synthesis,The 0.94(K0.4-xNa0.6BaxNb1-xZrx)O3-0.06LiSbO3 cera ... samples were sintered at 1050-1140 degC for 2-3 h.
43,10.1111/j.1551-2916.2009.03432.x,solid_state_ceramic_synthesis,0.3Pb(Ni1/3Nb2/3)O3-xPbTiO3-(0.7-x)PbZrO3 with x=0 ... 000deg and 1280degC in a covered alumina crucible.
44,10.1007/s10854-016-5228-4,solid_state_ceramic_synthesis,"Specimens with x = 0.1, 0.2, 0.25, 0.3 and 0.4 of  ... r, then sintered at 1450-1620 degC for 4 h in air."
45,10.1111/j.1551-2916.2008.02607.x,solid_state_ceramic_synthesis,"The ceramics based on Ba0.6Sr0.4TiO3-MgAl2O4 speci ... der, and then sintered at 1500degC for 4 h in air."
46,10.1007/s10854-013-1234-y,solid_state_ceramic_synthesis,The powders of Bi2Ti4O11 were prepared by conventi ...  for 2 h in air with a heating rate of 5 degC/min.
47,10.1007/s10853-009-3850-8,solid_state_ceramic_synthesis,The single-phase CCTO polycrystalline powder was p ... s the electrodes and fired at 600 degC for 15 min.
48,10.1007/s11661-013-2054-7,solid_state_ceramic_synthesis,Ferrite composites with ferrimagnetic phases have  ...  ball milled for 10 hours to obtain a fine powder.
49,10.1007/s10854-016-5314-7,solid_state_ceramic_synthesis,"In this work, Na1/3Ca1/3Y1/3Cu3Ti4O12 (NCYCTO) cer ... ce, and then cooled to room temperature naturally."
50,10.1016/j.ssi.2011.02.016,solid_state_ceramic_synthesis,Compositions with 1M4+10ScSZ (M4+ = Ce and Hf) wer ... ned to be 96% of the theoretical density or above.
51,10.1007/s10854-014-1915-1,solid_state_ceramic_synthesis,"(Ba1-x,Srx)(Zr0.1,Ti0.9)O3 ceramic samples were pr ... f the ceramics at 600 degC to form the electrodes."
52,10.1016/j.matdes.2016.12.006,solid_state_ceramic_synthesis,The conventional solid-state method was applied in ... ature ranging from 1050 degC to 1180 degC for 2 h.
53,10.1007/s10854-015-3725-5,solid_state_ceramic_synthesis,Dy2/3Cu3Ti4O12 ceramics were prepared by a standar ... ensity) and were applied in further investigation.
54,10.1007/s10854-013-1682-4,solid_state_ceramic_synthesis,"Reagent grade Na2CO3, K2CO3, Li2CO3, Nb2O5, Bi2O3, ... sealed alumina crucible to prevent volatilization."
55,10.1016/j.mseb.2012.09.004,solid_state_ceramic_synthesis,Ceramic samples were prepared by conventional soli ...  were muffled with powder of the same composition.
56,10.1016/j.ijhydene.2014.05.150,solid_state_ceramic_synthesis,SrCo0.7Fe0.2Ta0.1O3-δ (SCFT) powders were synthesi ...  for 10 h in air to obtain the dense LSGM pellets.
57,10.1016/j.jallcom.2007.11.055,solid_state_ceramic_synthesis,Analytical reagent grade powders (purity 99.99%) o ... cooled to the room temperature along with furnace.
58,10.1007/s10854-017-6802-0,solid_state_ceramic_synthesis,(Ba1-αCaα) Sm2Ti4O12 ceramic samples with α = 0.01 ...  of 100 degC/h was executed till room temperature.
59,10.1111/j.1551-2916.2009.03453.x,solid_state_ceramic_synthesis,Ba4Sm2Ti4Ta6O30 and Ba5SmTi3Ta7O30 ceramics were s ... range from 1673 to 1723 K to yield dense ceramics.
60,10.1016/j.jpcs.2011.06.008,solid_state_ceramic_synthesis,"First, the starting materials of Y2O3, V2O5, and E ... d at 1000 degC for 3 hr in a programmable furnace."
61,10.1016/j.jallcom.2013.06.009,solid_state_ceramic_synthesis,"BiFeO3 (BFO) samples were prepared through the sol ...  at 810 degC for 1 h in air, as described in [13]."
62,10.1016/j.matlet.2016.04.212,solid_state_ceramic_synthesis,The BYS samples were prepared by solid-state react ... for 4 h at heating rate of 4 degC /min in the air.
63,10.1007/s10854-011-0335-8,solid_state_ceramic_synthesis,"The (1-x)(BiScO3-0.64PbTiO3)-xLiNbO3 (BSPT64-xLN,  ... e loss of PbO and Bi2O3 caused by its sublimation."
64,10.1007/s10853-013-7419-1,solid_state_ceramic_synthesis,Pb0.97La0.02(ZrxSn0.9-xTi0.1)O3 (0.61 <= x <= 0.65 ...  both sides of the samples at 550 degC for 10 min.
65,10.1016/j.elecom.2014.09.006,solid_state_ceramic_synthesis,A garnet cylinder with the nominal chemical formul ...  sintered at 1140 degC for 16 h in air atmosphere.
66,10.1016/j.jeurceramsoc.2006.11.037,solid_state_ceramic_synthesis,The powders were prepared by conventional mixed ox ... pecimens was determined by the Archimedes' method.
67,10.1016/j.matdes.2016.08.046,solid_state_ceramic_synthesis,"Powders and ceramic samples with composition [Pb1  ... tered at this temperature, with the same protocol."
68,10.1016/j.mseb.2010.04.039,solid_state_ceramic_synthesis,The Ba(Ti1-xSnx)O3 nanocrystalline powders were sy ...  by sintering at temperature of 1350 degC for 4 h.
69,10.1016/j.jeurceramsoc.2017.02.053,solid_state_ceramic_synthesis,"ZrO2 (Shanghai Aladdin Co. Ltd., purity of 99.99%) ... ature increase rates were about 5 degC per minute."
70,10.1007/s10853-016-9922-7,solid_state_ceramic_synthesis,(100-x) at.% Ba0.6Sr0.4TiO3-x at.% Y2O3 (BST/Y2O3) ...  ceramics reached 95 % of the theoretical density.
71,10.1007/s10008-005-0647-9,solid_state_ceramic_synthesis,"The starting powders of Ba5-xNa2xNb10O30, where x= ... old isostatic pressing (CIP) at 100 MPa for 3 min."
72,10.1016/j.mseb.2014.03.003,solid_state_ceramic_synthesis,Aurivillius oxides (K0.16Na0.84)0.5Bi4.5Ti4O15 + x ... d by alumina crucible followed by furnace cooling.
73,10.1016/j.jssc.2004.08.003,solid_state_ceramic_synthesis,Ba5LaTi2Nb3O18 and Ba4La2Ti3Nb2O18 were synthesize ... ynthesis could be represented by Eqs. (1) and (2).
74,10.1016/j.jpowsour.2010.09.056,solid_state_ceramic_synthesis,(Sm1-xDyx)2Zr2O7 (0 <= x <= 1.0) ceramics were pre ... ular weight in a unit cell and lattice parameters.
75,10.1007/s10854-015-2986-3,solid_state_ceramic_synthesis,A MgCuZn ferrite with composition of (Mg0.2Cu0.25Z ... a circular ring shape for further sintering study.
76,10.1016/j.mseb.2015.06.011,solid_state_ceramic_synthesis,"(Ba0.4Ca0.6)1-xErxTiO3 (abbreviated as BCT-xEr, x  ... 0-1550 degC for 4 h in an alumina crucible in air."
77,10.1016/j.jpowsour.2011.05.009,solid_state_ceramic_synthesis,The Ce-doped BCN18 samples were prepared by a conv ... or 5 h in air with a heating rate of 2 degC min-1.
78,10.1016/j.jeurceramsoc.2006.04.012,solid_state_ceramic_synthesis,"All Zn1-x-yAlxTiyO (0 <= x <= 0.05, 0 <= y <= 0.02 ... 1400 degC for 20 h in air and then furnace cooled."
79,10.1016/j.physb.2010.09.027,solid_state_ceramic_synthesis,Sr1-xPrxTiO3 ceramics (0.00<=x<=0.07) were prepare ... ellets were sintered at 1325 degC in air for 10 h.
80,10.1007/s10854-011-0322-0,solid_state_ceramic_synthesis,"(1 - x)K0.49Na0.51NbO3 + xLiSbO3 (abbreviated as K ... ers and then sintered at 1,060-1,120 degC for 2 h."
81,10.1007/s10854-014-1824-3,solid_state_ceramic_synthesis,This 0.95(K0.5Na0.5)NbO3-0.05(Bi0.5K0.5)Zr1-xTixO3 ... e conducted on aged specimens (24 h after poling).
82,10.1007/s10854-014-1897-z,solid_state_ceramic_synthesis,Na2BiMg2V3O12 ceramics were prepared by the conven ... in and then cooled in furnace to room temperature.
83,10.1016/j.physb.2009.04.045,solid_state_ceramic_synthesis,"Samples with nominal composition of (ZnO)1-x(MnO2) ...  2 h, and then furnace-cooled to room temperature."
84,10.1007/s10854-014-2224-4,solid_state_ceramic_synthesis,"CaSiO3 powders were prepared by a routine solid-st ... e temperatures of 1,250-1,400 degC for 2 h in air."
85,10.1016/j.matchemphys.2011.11.039,solid_state_ceramic_synthesis,"The (NaxBi0.5)0.94Ba0.06TiO3 (x = 0.54, 0.50, 0.46 ... ed alumina crucibles during the sintering process."
86,10.1111/j.1551-2916.2008.02623.x,solid_state_ceramic_synthesis,"All samples in this study were prepared by solid-s ... 150degC for 3-9 h in air, O2 and N2, respectively."
87,10.1007/s10854-012-0868-5,solid_state_ceramic_synthesis,"High-purity Li2CO3 (+98.5 %), H3BO3 (+99 %), ZnO ( ... tures in the range of 875-925 degC for 3 h in air."
88,10.1007/s10854-010-0080-4,solid_state_ceramic_synthesis,"BaTi0.9Sn0.1O3 ceramics with 0, 0.2, 1 and 2 at.%  ... n0.1O3 were sintered at 1,350 degC for 2 h in air."
89,10.1016/j.jeurceramsoc.2016.05.002,solid_state_ceramic_synthesis,Ca0.6Sr0.4TiO3 ceramics with HfO2 additives (0 wt. ... sure of 200 MPa and sintered at 1400 degC for 2 h.
90,10.1007/s10854-010-0261-1,solid_state_ceramic_synthesis,(1-x)K0.49Na0.51NbO3 + xLiNbO3 (abbreviated as KNN ... nders and then sintered at 1060-1120 degC for 2 h.
91,10.1016/j.tsf.2008.04.031,solid_state_ceramic_synthesis,Pure and doped BST ceramics with various Sr conten ...  method was used for ceramic density measurements.
92,10.1016/j.matlet.2005.10.076,solid_state_ceramic_synthesis,"The preparation of PNNT/NiCuZn composites was desc ... 0 degC and 1050 degC for 2 h in air, respectively."
93,10.1007/s10854-016-5256-0,solid_state_ceramic_synthesis,The samples were prepared through conventional sol ... or 6 h in air with the heating rate of 5 degC/min.
94,10.1007/s10854-011-0404-z,solid_state_ceramic_synthesis,"(1 - x) Ca4La2Ti5O17 (CLTO)-xLaAlO3 ceramic sample ... mized sintering temperature of 1,560 degC for 4 h."
95,10.1016/j.matlet.2015.01.070,solid_state_ceramic_synthesis,The samples were separately by conventional solid- ...  at temperatures of 1330-1450 degC for 4 h in air.
96,10.1016/j.matlet.2012.08.063,solid_state_ceramic_synthesis,"High-purity Li2CO3 (+98.5%), TiO2 (+99%), H3BO3 (+ ... ness and then sintered at 850 degC in air for 3 h."
97,10.1016/j.matchemphys.2005.08.022,solid_state_ceramic_synthesis,"Ferrites with chemical formula of NiAlxFe2-xO4, wh ... ts were further cooled at the rate of 80 degC h-1."
98,10.1016/j.jeurceramsoc.2006.04.049,solid_state_ceramic_synthesis,The La9Sr1Si6O26.5 electrolyte powder was prepared ... e referred to as respectively CERM1/1 and CERM1/3.
99,10.1007/s10854-008-9600-x,solid_state_ceramic_synthesis,Specimens of the LNT ceramics were prepared by a c ... LV were sintered at 1050-1150 degC for 2 h in air.
100,10.1016/j.mseb.2009.01.002,solid_state_ceramic_synthesis,The pure CCTO powder was synthesized using the tra ... s the electrodes and fired at 600 degC for 15 min.
101,10.1016/j.jeurceramsoc.2015.05.002,solid_state_ceramic_synthesis,(Bi0.5Na0.5)TiO3 (BNT) and (Bi0.5Na0.5)0.925Ba0.07 ...  at 600 degC for 30 min to remove residual stress.
102,10.1007/s10854-014-1726-4,solid_state_ceramic_synthesis,"High quality LixSc0.02Ni0.98-xO ceramics with x =  ... ly, and then cooled to room temperature naturally."
103,10.1016/j.matlet.2005.05.053,solid_state_ceramic_synthesis,The Ca[(Li0.33Nb0.67)0.9Ti0.1]O3-δ powder composit ... or 3 h with 2.5 degC/min heating and cooling rate.
104,10.1111/j.1551-2916.2009.03429.x,solid_state_ceramic_synthesis,The starting materials were high-purity (better th ... s ranging from 1050deg to 1300degC for 4 h in air.
105,10.1016/j.matchemphys.2010.01.052,solid_state_ceramic_synthesis,Polycrystalline ceramic samples were prepared by s ...  degC in air for 3 h to obtain the dense ceramics.
106,10.1016/j.actamat.2009.06.011,solid_state_ceramic_synthesis,"Ba1-xSrxTiO3 (x = 0.4, 0.5, 0.6 and 0.7) ceramics  ... der and then sintered at 1400 degC for 4 h in air."
107,10.1111/j.1551-2916.2005.00581.x,solid_state_ceramic_synthesis,"Polycrystalline samples of V-doped InTaO4 (InTa1-x ... d at 1200degC for 6 h, and then thoroughly ground."
108,10.1016/j.jmmm.2005.05.033,solid_state_ceramic_synthesis,NiCuZn ferrites with compositions of Ni0.24Zn0.56C ... pecimens were sintered in air at 930 degC for 2 h.
109,10.1016/j.jpowsour.2015.10.030,solid_state_ceramic_synthesis,BaIn0.3Ti0.7O2.85 (BIT07) was synthesized by solid ...  acetone and was passed through 100 μm mesh sieve.
110,10.1016/j.matlet.2012.12.091,solid_state_ceramic_synthesis,The LMZT compositions were synthesized by the conv ... 60 degC for 3 h at a heating rate of 2.5 degC/min.
111,10.1007/s10854-008-9798-7,solid_state_ceramic_synthesis,Ceramic samples of composition Ba3Ti4-x(Fe1/2Nb1/2 ...  for 2 h with 5 degC/min heating and cooling rate.
112,10.1007/s10854-014-2182-x,solid_state_ceramic_synthesis,"Sr1-1.5xSmxTiO3 ceramics were prepared by a solid- ... binders and sintered at 1,400 degC for 3 h in air."
113,10.1016/j.matchemphys.2005.08.006,solid_state_ceramic_synthesis,Samples of CuO-doped Ba(Zn1/3Ta2/3)O3-BaZrO3 were  ... d the cooling rate were both set at 10 degC min-1.
114,10.1016/j.solidstatesciences.2003.10.001,solid_state_ceramic_synthesis,Mixtures with the Y/Ce atomic ratio range of 0.05- ... ons used were aged at 1000 degC in air for 8 days.
115,10.1111/j.1551-2916.2009.03303.x,solid_state_ceramic_synthesis,"The traditional solid-state reaction was used to p ... ensate the loss of Li, Na, and K during sintering."
116,10.1016/j.jallcom.2015.01.026,solid_state_ceramic_synthesis,"Ba(CoTi)1.2Fe9.6O19 M-type hexaferrites with vario ... , and finally sintered at 925 degC for 3 h in air."
117,10.1007/s10854-016-4601-7,solid_state_ceramic_synthesis,Samples were prepared by conventional solid-state  ... gC for 4 h in air at a heating rate of 5 degC/min.
118,10.1007/s10854-014-1755-z,solid_state_ceramic_synthesis,Li1+2xMg4-xV3O12 ceramics were prepared by the con ... ples were sintered at 680-900 degC for 4 h in air.
119,10.1007/s10854-014-1704-x,solid_state_ceramic_synthesis,"Sr[(Fe0.5Nb0.5)1-xTix]O3 (x = 0, 0.2, 0.4, 0.6 and ... e obtained by sintering at 1,673 K in air for 3 h."
120,10.1016/j.jmmm.2013.11.005,solid_state_ceramic_synthesis,Ni1-xZnxFe2O4 (0<=x<=1.0) ferrite powder was prepa ... on technology at the same temperature for 120 min.
121,10.1111/j.1551-2916.2006.01227.x,solid_state_ceramic_synthesis,The ceramic specimens were prepared by a conventio ... ating rate of 3degC/min and cooled in the furnace.
122,10.1111/j.1551-2916.2012.05327.x,solid_state_ceramic_synthesis,Calcium bismuth niobate powders were prepared by c ... h different grain sizes are summarized in Table 1.
123,10.1016/j.matlet.2012.04.120,solid_state_ceramic_synthesis,Specimens of the Li2Cu0.1Zn0.9Ti3O8 ceramics were  ... ating rate of the sintering process is 5 degC/min.
124,10.1007/s10854-015-4112-y,solid_state_ceramic_synthesis,The ceramics were prepared through a conventional  ... or 4 h in air with the heating rate of 5 degC/min.
125,10.1002/pssa.201330345,solid_state_ceramic_synthesis,The GZO target was synthesized by using a conventi ... egC for 5 h and then sintered at 950 degC for 5 h.
126,10.1016/j.matlet.2006.02.070,solid_state_ceramic_synthesis,"The ceramics were prepared using the conventional  ... g rate of 3 degC/min, and cooled with the furnace."
127,10.1016/j.jeurceramsoc.2007.02.194,solid_state_ceramic_synthesis,The material compositions used in this study are x ... and subsequently pressed into disks under 300 MPa.
128,10.1007/s10854-014-2368-2,solid_state_ceramic_synthesis,"The (1 - x)Ba0.75Sr0.25TiO3+xLa0.5Na0.5TiO3 cerami ... emperatures in the range from 1,400 to 1,450 degC."
129,10.1016/j.jeurceramsoc.2016.11.023,solid_state_ceramic_synthesis,Lead-free (1-x)(Bi0.5Na0.5)TiO3-xSrTiO3 (BNT-STx;  ... s were poled at 2.4 kV for 30 min in silicone oil.
130,10.1007/s10854-014-2612-9,solid_state_ceramic_synthesis,Samples of the LiMgVO4 ceramic was synthesized by  ...  for 4 h in air with a heating rate of 5 degC/min.
131,10.1111/j.1551-2916.2007.01937.x,solid_state_ceramic_synthesis,"Bulk BiFeO3 powder was prepared by a solid-state r ...  on an alumina disk, and fired at 825degC for 8 h."
132,10.1007/s10854-015-2697-9,solid_state_ceramic_synthesis,A NiCuZn ferrite with composition of (Ni0.15Cu0.2Z ...  in a circular ring shape for the sintering study.
133,10.1016/j.matlet.2006.11.095,solid_state_ceramic_synthesis,Samples of Ba5Nb4-xVxO15 with x = 0-1 were synthes ... emperatures from 1050 to 1200 degC for 4 h in air.
134,10.1007/s10854-016-4697-9,solid_state_ceramic_synthesis,Samples of the Ca5Mn4(VO4)6 ceramics were synthesi ...  for 5 h in air with a heating rate of 5 degC/min.
135,10.1016/j.jeurceramsoc.2005.03.091,solid_state_ceramic_synthesis,"The polycrystalline ceramic materials Pb1 - xSrxTi ... xygen atmosphere, to prevent possible loss of PbO."
136,10.1016/j.matlet.2014.08.133,solid_state_ceramic_synthesis,"(1-x)(0.65BiFeO3-0.35BaTiO3)-xNb2O5 (x=0, 1, 3, 5  ... C, 950 degC, 975 degC, and 975 degC, respectively."
137,10.1016/j.materresbull.2010.05.002,solid_state_ceramic_synthesis,"The (Ba0.6Sr0.4)1-xLaxCo0.4Fe0.6O3-δ (x = 0, 0.1)  ... any agglomerations during the calcination process."
138,10.1016/j.jeurceramsoc.2006.04.174,solid_state_ceramic_synthesis,The ceramics were prepared using the conventional  ... ets were sintered at temperatures at 840-920 degC.
139,10.1007/s10854-009-9901-8,solid_state_ceramic_synthesis,Specimens of the (Li1/2Nd1/2)WO4 ceramics were pre ... lets were sintered at 725-850 degC for 4 h in air.
140,10.1007/s10854-017-6403-y,solid_state_ceramic_synthesis,Sr doped Barium (Ba0.9Sr1-xTi0.6Zr0.3 Mn0.1O3) (wi ... d powder and it was sintered to 1600 degC for 5 h.
141,10.1016/j.mseb.2014.09.001,solid_state_ceramic_synthesis,"In order to accelerate the solid-state reaction, t ... These samples were sintered at 1650 degC for 12 h."
142,10.1007/s10854-016-6092-y,solid_state_ceramic_synthesis,MAT ceramics were prepared by the conventional sol ... in and then cooled to room temperature in furnace.
143,10.1111/j.1551-2916.2008.02871.x,solid_state_ceramic_synthesis,Ceramics with compositions of (Na0.52K0.48-x)(Nb1- ...  then sintered in air at 1060deg-1120degC for 3 h.
144,10.1111/j.1551-2916.2009.03298.x,solid_state_ceramic_synthesis,"Ceramic specimens were prepared by the conventiona ... degC for 40 h, and 970degC for 10 h, respectively."
145,10.1007/s10854-011-0372-3,solid_state_ceramic_synthesis,"SrLa4-xSmxTi5O17 compositions (x = 0, 1, 2, 3, or  ... t 20 kV, was used for microstructural examination."
146,10.1016/j.jallcom.2011.06.025,solid_state_ceramic_synthesis,Ba0.65Sr0.35TiO3 ceramics were fabricated by the c ... pellets were sintered at 1350 degC for 4 h in air.
147,10.1007/s10854-016-4671-6,solid_state_ceramic_synthesis,The specimens in the (0.67-x)BiFeO3-0.33PbTiO3-xBa ... ets to decrease the evaporation loss of Pb and Bi.
148,10.1016/j.actamat.2016.11.001,solid_state_ceramic_synthesis,The SrBi2(Nb0.2Ta0.8)2O9 and SrBi1.85Pr0.15(Nb0.2T ... % of the theoretical density for all the ceramics.
149,10.1016/j.jeurceramsoc.2014.03.001,solid_state_ceramic_synthesis,The substituted barium zirconates BaCe0.5Zr0.4Y0.1 ... ers were milled again for 24 h as described above.
150,10.1016/j.jeurceramsoc.2006.04.167,solid_state_ceramic_synthesis,"Samples of compositions SrBi2(WxTa1-x)2O9 (SBWT),  ... pellets were sintered at 1150 degC for 2 h in air."
151,10.1016/j.matlet.2008.10.035,solid_state_ceramic_synthesis,The LCMO/Al2O3 (x = 0; 0.01; 0.02; 0.03; 0.04 and  ... re of 10 MPA/cm2 and sintered at 900 degC for 3 h.
152,10.1007/s10854-009-9922-3,solid_state_ceramic_synthesis,A conventional mixed oxide route was utilized to p ... silicon oil at 80 degC under 3-4 kV/mm for 15 min.
153,10.1016/j.matlet.2011.08.054,solid_state_ceramic_synthesis,"Powder samples of Ca3 - xSi2O7: xEu2+ (0 <= x <= 0 ... es, the disk was ground to powder for measurement."
154,10.1111/j.1744-7402.2009.02400.x,solid_state_ceramic_synthesis,Samples of (Mg0.95Ni0.05)TiO3 and (La0.5Na0.5)TiO3 ...  rate and the cooling rate were set at 10degC/min.
155,10.1016/j.ceramint.2013.05.056,solid_state_ceramic_synthesis,"SrBi2-xHoxTa2O9 compositions with x=0.0, 0.01, 0.0 ... pellets were sintered at 1200 degC for 2 h in air."
156,10.1016/j.jeurceramsoc.2005.02.006,solid_state_ceramic_synthesis,"CaBi4-xNdxTi4O15 ceramics with x = 0, 0.25, 0.5, 0 ... e densest ceramics were attained increased with x."
157,10.1007/s10854-012-0743-4,solid_state_ceramic_synthesis,"For the pure BaTi5O11 ceramic, it is very difficul ...  heat rate of the sintering process is 5 degC/min."
158,10.1111/j.1744-7402.2008.02352.x,solid_state_ceramic_synthesis,Samples of MNT and ST were individually synthesize ...  and the cooling rate were both set at 10degC/min.
159,10.1007/s10854-016-4938-y,solid_state_ceramic_synthesis,"The Mg1-xNixTiO3 (x = 0.00-0.07) ceramics are prep ... cooling rates are 15 and 1 degC/min, respectively."
160,10.1016/j.fusengdes.2015.05.061,solid_state_ceramic_synthesis,Li2TiO3 powder was synthesized by solid-state reac ...  air atmosphere. The reaction is shown in Eq. (1).
161,10.1007/s10854-011-0489-4,solid_state_ceramic_synthesis,Ba0.95Ca0.05TiO3 ceramics with different doping co ... ubsequently reoxidized at 900 degC in air for 2 h.
162,10.1007/s10854-015-3008-1,solid_state_ceramic_synthesis,"Samples of MgTiO3 and CaTiO3 were individually syn ...  degC for 4 h (for 95MCT-y wt% LBS), respectively."
163,10.1007/s10854-014-1760-2,solid_state_ceramic_synthesis,"(Ca0.8Sr0.2)ZrO3 ceramics were prepared through a  ... egC/min for 2, 4, 6, 8, 10 and 12 h, respectively."
164,10.1016/j.mseb.2007.05.002,solid_state_ceramic_synthesis,"Polycrystalline La0.67Ca0.33Mn1-x-BxO3 (x = 0, 0.1 ...  room temperature at a cooling rate of 3 degC/min."
165,10.1016/j.matlet.2016.05.009,solid_state_ceramic_synthesis,CoTiNb2O8 and CoNb2O6 compounds were individually  ... 75 degC for 4 h with a heating rate of 5 degC/min.
166,10.1016/j.ssc.2012.03.007,solid_state_ceramic_synthesis,The BBT ceramics was prepared by the standard soli ... d by alumina crucible followed by furnace cooling.
167,10.1016/j.mseb.2010.12.007,solid_state_ceramic_synthesis,Ceramic powders with nominal formula (1 - x)Bi0.5N ... both faces of the disks at 650 degC as electrodes.
168,10.1016/j.tsf.2008.12.040,solid_state_ceramic_synthesis,Ca1 - xPrxTiO3 ceramic target with x = 0.2 mol% wa ...  degC for 4 h in a Nabertherm furnace (LHT 04/17).
169,10.1016/j.jssc.2014.06.009,solid_state_ceramic_synthesis,"Al2-2x(ZrMg)xW3O12 (x=0, 0.1, 0.3, 0.5, 0.7, 0.8,  ... lowed by sintering at 1373 K for 4 h in a furnace."
170,10.1016/j.ssc.2007.02.025,solid_state_ceramic_synthesis,Ceramic specimens are prepared by the conventional ... e sintered disks and fired at 570 [?]C for 20 min.
171,10.1016/j.jallcom.2015.05.005,solid_state_ceramic_synthesis,"[Ba1-xSrx](Zr0.05Ti0.95)O3 ceramics [x = 0, 0.1, 0 ... 1100 degC for 4 h by using a programmable furnace."
172,10.1007/s10854-010-0140-9,solid_state_ceramic_synthesis,"Ca1-3x/2NdxCu3Ti4O12 (x = 0, 0.1, 0.2) ceramics we ... 0 degC in air for 3 h to yield the dense ceramics."
173,10.1016/j.ceramint.2016.12.143,solid_state_ceramic_synthesis,"BT and BT doped with 1 and 2 mol% Zr, denoted BZT1 ... LT) of 1200-1300 degC, with dwell times of 3-10 h."
174,10.1016/j.jmmm.2014.07.060,solid_state_ceramic_synthesis,All the compositions of Co0.7-xNixMn0.3Fe2O4 (with ...  cooling was adopted for both the heat treatments.
175,10.1007/s10854-014-1762-0,solid_state_ceramic_synthesis,"[(Bi0.5Na0.5)0.94Ba0.06]1-xSrxTiO3 (x = 0, 0.025,  ... ,423 K in air for 3 h to yield the dense ceramics."
176,10.1016/j.matlet.2009.03.053,solid_state_ceramic_synthesis,[(Na0.7K0.2Li0.1)0.5Bi0.5]TiO3 ceramics (abbreviat ... hed sample was thermal etched for SEM examination.
177,10.1016/j.matlet.2015.06.113,solid_state_ceramic_synthesis,The specimens were manufactured using a convention ... er a dc electric field of 3 kV/mm in silicone oil.
178,10.1002/pssa.200510005,solid_state_ceramic_synthesis,Nb-doped bismuth titanate (Bi4Ti2.98Nb0.02O12) cer ... tive density of over 95% of the theoretical value.
179,10.1007/s10853-011-5842-8,solid_state_ceramic_synthesis,"2LN-BS-xPT (x = 0.58-0.66) ceramics were prepared  ... s of PbO, Bi2O3, and Li2CO3 caused by sublimation."
180,10.1007/s10854-014-2596-5,solid_state_ceramic_synthesis,Superconducting samples with chemical composition  ... n furnace up to room temperature after each cycle.
181,10.1007/s10854-016-5551-9,solid_state_ceramic_synthesis,"Lead free (K0.5Na0.5)(Nb1-xVx)O3 (x = 0, 0.01, 0.0 ... ed as KNNV0, KNNV1, KNNV2, KNNV3, KNNV4 and KNNV5."
182,10.1007/s10854-016-5252-4,solid_state_ceramic_synthesis,CoNb2O6 ceramics were synthesized by conventional  ... te and cooling rate were maintained at 3 degC/min.
183,10.1016/j.enconman.2006.11.005,solid_state_ceramic_synthesis,La0.2Sr0.8TiO3 (LST) powder was prepared by solid  ... in argon for electrical conductivity measurements.
184,10.1016/j.jeurceramsoc.2011.04.023,solid_state_ceramic_synthesis,The (Ba0.85Ca0.15)(Ti0.9Zr0.1)O3 (BCTZ) ceramics w ... ts were sintered at 1500-1550 degC for 2 h in air.
185,10.1016/j.jallcom.2013.07.187,solid_state_ceramic_synthesis,"Polycrystalline Bi0.8Ba0.2FeO3 (BBFO), Bi0.8Ba0.2F ... ed uniformly with silver paste to make electrodes."
186,10.1007/s10854-010-0097-8,solid_state_ceramic_synthesis,"La2NiMnO6 dense ceramic targets were prepared by a ... e obtained by sintering at 1,748 K in air for 3 h."
187,10.1016/j.jeurceramsoc.2006.02.009,solid_state_ceramic_synthesis,Twenty different compositions were prepared in the ... eity and then calcined again at 850 degC for 10 h.
188,10.1007/s10853-010-4723-x,solid_state_ceramic_synthesis,Polycrystalline samples of 1Ce10ScSZ were synthesi ... ted to be 96% of the theoretical density or above.
189,10.1111/j.1551-2916.2005.00633.x,solid_state_ceramic_synthesis,"In the experiment, PNNT and NiCuZn were prepared s ... d at 950deg, 1000deg, and 1050degC for 2 h in air."
190,10.1111/j.1551-2916.2007.01925.x,solid_state_ceramic_synthesis,"Sample powders of (1-x)Ca(Mg1/3Nb2/3)O3-(x)CaZrO3; ... , the density was >99.0% of the theoretical value."
191,10.1016/j.matchemphys.2007.06.017,solid_state_ceramic_synthesis,The ceramic specimens of Ba(Zr0.15Ti0.85)O3 were p ... red ceramic specimens for dielectric measurements.
192,10.1111/j.1551-2916.2008.02831.x,solid_state_ceramic_synthesis,"Samples of the (Mg0.95M0.052+)Ti2O5 (M2+=Co, Ni, a ...  rate and the cooling rate were set at 10degC/min."
193,10.1002/pssr.200802023,solid_state_ceramic_synthesis,"The pure NBT ceramics were produced using a conven ...  x wt% CeO2, where x = 0.25, 0.50, 0.75, and 1.00."
194,10.1016/j.matchemphys.2011.01.009,solid_state_ceramic_synthesis,FeVO4 was synthesised by a conventional solid stat ...  221 MPa and sintered in air at 590 degC for 24 h.
195,10.1007/s10854-011-0416-8,solid_state_ceramic_synthesis,Conventional solid state ceramic route is used to  ...  samples are measured using the Archimedes method.
196,10.1007/s10854-013-1150-1,solid_state_ceramic_synthesis,"The LZT samples were synthesized by the convention ... ,175 degC for 4 h at a heating rate of 5 degC/min."
197,10.1007/s10854-015-3235-5,solid_state_ceramic_synthesis,We have synthesized the polycrystalline samples Pr ... o room temperature to maximize the oxygen content.
198,10.1016/j.ssi.2008.01.096,solid_state_ceramic_synthesis,Samples have been prepared by using the solid stat ... ides of the disk were polished with a 3 μm polish.
199,10.1016/j.jeurceramsoc.2013.03.026,solid_state_ceramic_synthesis,"Reagent-grade SrO, Fe2O3 and MoO3 from Sigma-Aldri ... ubsequently annealed at 1200 degC, 2 h in 5%H2/Ar."
200,10.1016/j.apsusc.2008.02.027,solid_state_ceramic_synthesis,The SBN ceramic targets were synthesized employing ...  closed Al2O3 crucible surrounded by ZrO2 powders.
201,10.1016/j.physb.2015.03.011,solid_state_ceramic_synthesis,The produced materials (Bi1/2Na1/2)0.94-x(Li1/2Ce1 ... into preprepared powder with the same composition.
202,10.1007/s10854-016-5549-3,solid_state_ceramic_synthesis,"BTTN_x ceramics were prepared by the solid state r ... y, they were sintered at 1080 degC for 2 h in air."
203,10.1016/j.matlet.2013.12.054,solid_state_ceramic_synthesis,"The polycrystalline BIT-SBTi: xEr3+ (x=0.0, 0.02,  ...  cm in diameter and sintered at 1200 degC for 1 h."
204,10.1016/j.electacta.2010.07.040,solid_state_ceramic_synthesis,"The specimens were prepared by the conventional so ... easurements and dip-immersion tests, respectively."
205,10.1016/j.jeurceramsoc.2012.02.048,solid_state_ceramic_synthesis,"In this work, CaCu3Ti4-xTaxO12 ceramics, where x = ...  these pellets were sintered at 1100 degC for 5 h."
206,10.1007/s10854-013-1364-2,solid_state_ceramic_synthesis,The (1 - x)BNT-xBS piezoelectric ceramics were pre ... ed into the corresponding powder during sintering.
207,10.1016/j.matlet.2015.10.043,solid_state_ceramic_synthesis,In order to compare the characteristics of the pur ... emperature (850 degC and 900 degC) for 4 h in air.
208,10.1016/j.jeurceramsoc.2009.12.018,solid_state_ceramic_synthesis,"A2+B6+O4 (A2+: Ca, Pb, Ba; B6+: Mo, W) was prepare ... ere sintered from 800 to 1100 degC for 3 h in air."
209,10.1016/j.ssc.2006.03.018,solid_state_ceramic_synthesis,BaTiO3 and Ba(Ti0.7Hf0.3)O3 ceramics were prepared ... y to room temperature while furnace power was off.
210,10.1016/j.jeurceramsoc.2005.09.016,solid_state_ceramic_synthesis,Specimens were prepared by a conventional mixed ox ...  approximately 15.5 mm in diameter and 9 mm thick.
211,10.1016/j.materresbull.2013.05.108,solid_state_ceramic_synthesis,Polycrystalline ceramics of (Ba0.85Ca0.15)(Ti0.9Zr ... t in the temperature range 1450-1500 degC for 3 h.
212,10.1016/j.jeurceramsoc.2005.03.049,solid_state_ceramic_synthesis,BSTZ targets were prepared by conventional solid-s ... hen sintered at temperature of 1400 degC for 12 h.
213,10.1016/j.ssc.2007.08.030,solid_state_ceramic_synthesis,Superconducting samples with chemical composition  ... n furnace up to room temperature after each cycle.
214,10.1016/j.mseb.2004.12.071,solid_state_ceramic_synthesis,"The (Zr0.8, Sn0.2)TiO4 ceramic materials were prep ... ing and then sintered at 1280-1400 degC for 2-4 h."
215,10.1016/j.solidstatesciences.2013.07.006,solid_state_ceramic_synthesis,"CaCO3 (99.0%), CuO (99%) and TiO2 (98%) were used  ... ellets were briefly called as U1-U5, respectively."
216,10.1016/j.jallcom.2014.11.134,solid_state_ceramic_synthesis,Lead-free (K0.485Na0.5Li0.015)(Nb0.9-xTa0.1Vx)O3 ( ... un wheel every 6 min after a rest period of 2 min.
217,10.1007/s10854-015-2746-4,solid_state_ceramic_synthesis,"The samples used in this study were prepared by so ... re sintered at temperatures of 1,150 degC for 2 h."
218,10.1111/j.1551-2916.2008.02744.x,solid_state_ceramic_synthesis,A sample of Nd[(Co1-xZnx)1/2Ti1/2]O3 was prepared  ... e cooling rate were both controlled at 10degC/min.
219,10.1016/j.jpowsour.2008.11.080,solid_state_ceramic_synthesis,"BaCe(0.9-x)ZrxY0.1O(3-δ) powders (x = 0, 0.3, 0.7  ... 350 MPa) and sintered in air at 1700 degC for 6 h."
220,10.1007/s10854-014-2436-7,solid_state_ceramic_synthesis,"Sample were separately synthesized by conventional ... t temperatures of 1,420-1,630 degC for 4 h in air."
221,10.1016/j.mseb.2012.12.010,solid_state_ceramic_synthesis,Specimens of (Ca0.8Sr0.2)(SnxTi1-x)O3 (x = 0.1-0.9 ...  at temperatures of 1390-1540 degC for 4 h in air.
222,10.1016/j.jpcs.2007.05.025,solid_state_ceramic_synthesis,Ferrite samples with chemical formula Zn1-xCoxFe2O ... 0 sample was sintered at 1200 degC for 5 h in air.
223,10.1016/j.ssc.2007.04.009,solid_state_ceramic_synthesis,"Samples of compositions Sr1-xEuxBi2Ta2O9 (SEBT), w ... pellets were sintered at 1200 [?]C for 2 h in air."
224,10.1016/j.ssi.2013.11.004,solid_state_ceramic_synthesis,La0.4Sr0.6Co1-xTaxO3-δ (x = 0 - 0.2) ceramic sampl ...  pellet was sintered at 1420 degC for 12 h in air.
225,10.1016/j.ssi.2015.07.008,solid_state_ceramic_synthesis,The BZY (BaZr0.8Y0.2O3 -δ) electrolyte was synthes ... orous and ready for molten carbonate infiltration.
226,10.1016/j.matlet.2004.08.005,solid_state_ceramic_synthesis,Samples of La(Co1/2Ti1/2)O3 were synthesized by co ... and the cooling rate were both set at 10 degC/min.
227,10.1016/j.jmbbm.2013.10.011,solid_state_ceramic_synthesis,"Ca3(PO4)2 was prepared by solid state reaction bet ... CaO, 0.38+-0.02 wt% of MgO, Ca/P molar ratio=1.52."
228,10.1016/j.matchemphys.2013.08.061,solid_state_ceramic_synthesis,BiFeO3 polycrystalline sample was synthesized by c ... thickness ~1 mm and sintered at 825 degC for 20 h.
229,10.1016/j.ssi.2004.06.010,solid_state_ceramic_synthesis,Samples obtained by solid state reaction: the deta ...  the pellets were heated at 1150 degC during 10 h.
230,10.1016/j.materresbull.2013.04.047,solid_state_ceramic_synthesis,FeTiNbO6 samples were prepared by the solid-state  ... annealed at 950 degC for 5 h in oxygen atmosphere.
231,10.1007/s10854-010-0095-x,solid_state_ceramic_synthesis,"BNT powders were prepared via a conventional mixed ... f 910degC to 1,010degC with an interval of 20degC."
232,10.1016/j.matlet.2008.09.017,solid_state_ceramic_synthesis,Samples of Nd(Zn1/2Ti1/2)O3 were prepared by a con ... cooling rate were both controlled at 10 degC /min.
233,10.1016/j.jallcom.2006.08.269,solid_state_ceramic_synthesis,"Samples of compounds of Eu3+, Sm3+, Dy3+-doped LaA ...  900-1300 degC for 12 h in a programmable furnace."
234,10.1016/j.optmat.2013.06.053,solid_state_ceramic_synthesis,For the comparison of the optical properties we ha ... ed at 750 degC for 2 h in dry nitrogen atmosphere.
235,10.1007/s00339-014-8952-8,solid_state_ceramic_synthesis,Ceramic samples of (1 - x)CaCu3Ti4O12-xBiFeO3 (x = ... 30 min for measurement of the electric properties.
236,10.1016/j.jmmm.2009.11.010,solid_state_ceramic_synthesis,The Ni-Cu-Zn ferrite samples were prepared by stan ... 00 degC in air for 3 h to yield the final samples.
237,10.1016/j.ssc.2009.08.016,solid_state_ceramic_synthesis,"The Sr1-xCuxBi2Nb2O9 samples (with x equal to 0.0, ...  an alumina crucible, followed by furnace cooling."
238,10.1007/s10853-011-6039-x,solid_state_ceramic_synthesis,Samples of (1 - x) Ca4La2Ti5O17-xNdAlO3 with x = 0 ... emperatures from 1500 to 1560 degC for 4 h in air.
239,10.1016/j.matlet.2015.11.131,solid_state_ceramic_synthesis,The BNBT- x SZMO (x=0-0.010) piezoelectric ceramic ... tions are similar as that reported elsewhere [20].
240,10.1007/s10854-016-5610-2,solid_state_ceramic_synthesis,"BMFT ceramics were prepared by a conventional soli ... using Bi2O3 (99 %), Fe2O3 (99 %) as raw materials."
241,10.1016/j.jallcom.2009.07.091,solid_state_ceramic_synthesis,LLTO precursor powder was prepared by conventional ... h with interval ball milling to obtain LLTO phase.
242,10.1016/j.ssi.2010.04.005,solid_state_ceramic_synthesis,Table 1 shows the abbreviations used to denote the ...  dense pellets without inhomogeneous grain growth.
243,10.1016/j.jeurceramsoc.2015.01.030,solid_state_ceramic_synthesis,Densities were also compared with the density of a ...  obtained using mechanosynthesized BiFeO3 powders.
244,10.1007/s10854-013-1544-0,solid_state_ceramic_synthesis,"The (Ba0.85Ca0.15) (Zr0.1Ti0.9)O3 - x wt% Sr(Cu1/3 ... red at a temperature of 1,380 degC for 4 h in air."
245,10.1016/j.matlet.2012.04.067,solid_state_ceramic_synthesis,All ceramic samples were prepared with the use of  ...  temperature dielectric and ferroelectric testing.
246,10.1007/s10854-015-3615-x,solid_state_ceramic_synthesis,Li2Zn(Ti1-xZrx)3O8 (x = 0-0.10) ceramics were prep ... n the temperature range of 1060-1140 degC for 4 h.
247,10.1016/j.jeurceramsoc.2005.06.025,solid_state_ceramic_synthesis,"The LSFG powder was synthesized through a solid-st ...  charge, dried and calcined at 1100 degC for 10 h."
248,10.1016/j.optmat.2014.01.017,solid_state_ceramic_synthesis,The Ce:LuAG scintillator ceramics were fabricated  ... -30 h and then air-annealed at 1450 degC for 20 h.
249,10.1007/s10854-013-1308-x,solid_state_ceramic_synthesis,"Ba6-3xLn8+2xTi18O54 (x = 1/4, 1/2, 2/3, 3/4) ceram ... ceramics were naturally cooled inside the furnace."
250,10.1007/s10854-014-2129-2,solid_state_ceramic_synthesis,"Polycrystalline samples of Ba1-xLax (Zr0.9Ti0.1)1- ... t 1,533 K, 1,653 K for 2 h in an alumina crucible."
251,10.1016/j.ssc.2006.09.047,solid_state_ceramic_synthesis,"The (Sr0.4Ba0.6)1-1.5xBixTiO3 ( x = 0.05 , abbrevi ...  for 4 h and cooled naturally to room temperature."
252,10.1016/j.jeurceramsoc.2010.10.024,solid_state_ceramic_synthesis,"Commercial Nb2O5 powder (Merck, 99.9%) was used as ... egC for 4 h with a rate temperature of 5 degC/min."
253,10.1111/j.1551-2916.2011.04522.x,solid_state_ceramic_synthesis,"For the purpose of comparison, EFO was also synthe ...  were at last sintered in 1100degC for 3 h in air."
254,10.1016/j.jeurceramsoc.2011.09.014,solid_state_ceramic_synthesis,CaSiO3 powders were prepared by a conventional sol ...  for 2 h in air with a heating rate of 5 degC/min.
255,10.1007/s10854-013-1390-0,solid_state_ceramic_synthesis,Polycrystalline samples of Bi1.8Sr2WxCa1.1Cu2.1Oy  ...  start the formation of the superconducting phase.
256,10.1016/j.jeurceramsoc.2016.03.002,solid_state_ceramic_synthesis,(0.75-x)BF-0.25PT-xPMN (x = 0.2-0.75) ceramics wer ... er paste and finally fired at 550 degC for 30 min.
257,10.1007/s10854-012-0910-7,solid_state_ceramic_synthesis,"Samples with compositions of (1 - x)Ba3(VO4)2-xCaW ... n the temperature range of 850-1,000 degC for 4 h."
258,10.1007/s10854-016-5526-x,solid_state_ceramic_synthesis,"The CaTi1-x(Al0.5Ta0.5)xO3 samples with x = 0.2, 0 ... inder and then sintered at 1480-1590 degC for 4 h."
259,10.1111/j.1551-2916.2008.02292.x,solid_state_ceramic_synthesis,Ba1-xLa2x/3(Zn0.3Co0.7)1/3Nb2/3O3 (0<=x<=0.06) cer ... composition. A cooling rate of 100degC/h was used.
260,10.1016/j.jpowsour.2014.10.178,solid_state_ceramic_synthesis,A Li2FeP2O7 sample is prepared by the conventional ... sintered at 600 degC for 12 h in argon atmosphere.
261,10.1007/s10854-013-1699-8,solid_state_ceramic_synthesis,5BaO-2V2O5 ceramic was prepared by conventional so ...  given at 600 degC for 30 min to expel the binder.
262,10.1111/j.1551-2916.2006.01312.x,solid_state_ceramic_synthesis,Samples of BLZN ceramic powder were prepared by us ... ion of powder to reduce ZnO loss during sintering.
263,10.1007/s10854-013-1460-3,solid_state_ceramic_synthesis,Nano powders of Ba(Zr0.15Ti0.85)O3 powders were sy ... mens was measured using the Archimedes' principle.
264,10.1016/j.jeurceramsoc.2011.05.010,solid_state_ceramic_synthesis,Na0.5Bi0.5TiO3 ceramic samples were prepared using ... 4 h with a heating and cooling rate of 5 degC/min.
265,10.1007/s10854-017-6670-7,solid_state_ceramic_synthesis,BaTiO3 ceramics were prepared by the conventional  ... temperature interval for 25 degC) for another 2 h.
266,10.1007/s10854-010-0177-9,solid_state_ceramic_synthesis,Ferrite composites with ferrimagnetic phases have  ... ther ball-milled for 10 h to obtain a fine powder.
267,10.1016/j.ssc.2003.12.024,solid_state_ceramic_synthesis,"The SrBi4-x/3Ti4-xVxO15 (SBTV-x, x=0.00, 0.003, 0. ... degC for 1.5 h in air followed by furnace cooling."
268,10.1016/j.mssp.2013.04.010,solid_state_ceramic_synthesis,"Zn1-xSnxO (x=0, 0.0625) powders were prepared by t ... cursors were calcined at 900 or 1000 degC for 2 h."
269,10.1016/j.ssi.2006.09.010,solid_state_ceramic_synthesis,La0.8Sr0.2Ga0.8Mg0.2O3 (LSGM) as the electrolyte w ... ss of 0.6 mm after sintering at 1500 degC for 5 h.
270,10.1007/s10854-011-0421-y,solid_state_ceramic_synthesis,Specimens of the Li2CoTi3O8 ceramics were prepared ... ating rate of the sintering process is 5 degC/min.
271,10.1007/s10854-015-3551-9,solid_state_ceramic_synthesis,"The produced materials CxSBN with x = 0.00, 0.10,  ... tered in an alumina crucible at 1100 degC for 2 h."
272,10.1016/j.physb.2014.04.062,solid_state_ceramic_synthesis,The samples of BIT and BSTF were prepared by the c ... intering of pellets was done at 1000 degC for 4 h.
273,10.1016/j.jeurceramsoc.2005.03.152,solid_state_ceramic_synthesis,Specimens were prepared by a conventional mixed ox ... ere approximately 15.5 mm diameter and 9 mm thick.
274,10.1016/j.apsusc.2005.11.059,solid_state_ceramic_synthesis,Target of SrRuO3 ceramic was made by conventional  ... 5 h to get the dense and crack-free SrRuO3 target.
275,10.1007/s10854-014-1725-5,solid_state_ceramic_synthesis,The LMZT compositions were prepared by the convent ... lets were sintered in air at 850-950 degC for 3 h.
276,10.1016/j.ssi.2008.02.011,solid_state_ceramic_synthesis,"Yttrium doped strontium zirconate, SrZr0.9Y0.1O3 - ...  at 300 MPa, and then sintered at 1973 K for 10 h."
277,10.1016/j.jallcom.2015.12.218,solid_state_ceramic_synthesis,"Na0.5Bi4.5Ti4-x (WNb)x/2O15 ceramics, were prepare ...  h in a sealed crucible to prevent volatilization."
278,10.1016/j.mseb.2010.10.016,solid_state_ceramic_synthesis,Li2+xTiO3 (0 <= x <= 0.2) ceramic samples were pre ...  were muffled with powder of the same composition.
279,10.1007/s10854-014-2003-2,solid_state_ceramic_synthesis,Nanopowders of (K0.485Na0.5Li0.015)(Nb0.9-xTa0.1Vx ...  wheel every 6 min after a rest interval of 2 min.
280,10.1007/s10854-013-1564-9,solid_state_ceramic_synthesis,"For sample No. 2, CCTO was prepared by the traditi ... om temperature in the conventional muffle furnace."
281,10.1016/j.matchemphys.2010.07.051,solid_state_ceramic_synthesis,LiY(W1-xTex)2O8 (0.0 <= x <= 0.2) ceramic samples  ...  were muffled with powder of the same composition.
282,10.1016/j.matchemphys.2011.03.043,solid_state_ceramic_synthesis,"xTM - (100 - x)/2BaWO4 (BW) - (100 - x)/2Ba0.5Sr0. ... m and 17/8 mm in diameter/thickness, respectively."
283,10.1016/j.jmmm.2015.04.087,solid_state_ceramic_synthesis,Various (1-y)BFO-yNCZFO composites were prepared b ... degC for 4 h in air for various characterizations.
284,10.1007/s10854-015-3916-0,solid_state_ceramic_synthesis,1 wt% Li2WO4-doped (1 - y)Zn2SnO4-yCa0.8Sr0.2TiO3  ... ing rate and cooling rate were set at 10 degC/min.
285,10.1016/j.jpowsour.2008.07.064,solid_state_ceramic_synthesis,Samples of SBCO were prepared with a conventional  ...  using the glycine-nitrate combustion method [30].
286,10.1016/j.powtec.2003.11.005,solid_state_ceramic_synthesis,"BIT was also prepared by solid state reaction to b ...  750 degC for 10 h, in an open atmosphere furnace."
287,10.1016/j.powtec.2015.02.035,solid_state_ceramic_synthesis,"Sr1 - xSixMnO3 - δ (x = 0.05, 0.1, 0.15, 0.2, and  ... bodies were sintered at 1400 degC for 10 h in air."
288,10.1016/j.matlet.2015.04.058,solid_state_ceramic_synthesis,A powder sample of Lu1.5Tb1.5Fe5O12 was synthesize ... obtained by sintering at 1300 degC for 5 h in air.
289,10.1111/j.1551-2916.2007.02222.x,solid_state_ceramic_synthesis,"Ten mole percent Y2O3-doped SrZrO3 (SrZr0.9Y0.1O2. ... 3, SZY10-Z4, SZY10-Z5, and SZY10-Z6, respectively."
290,10.1016/j.ssc.2010.05.029,solid_state_ceramic_synthesis,La2NiMnO6 ceramics were prepared by a solid state  ... ets were 1.5 mm in height and 8.21 mm in diameter.
291,10.1016/j.matchemphys.2016.01.047,solid_state_ceramic_synthesis,Multiferroic materials with the compositional form ...  pellets were sintered at 850 degC for 4 h in air.
292,10.1007/s10854-016-5493-2,solid_state_ceramic_synthesis,The materials BNT-BT6.5-xSCN were prepared by the  ... oss of bismuth and sodium oxides during sintering.
293,10.1016/j.jallcom.2009.07.106,solid_state_ceramic_synthesis,(Na0.53K0.4Li0.07)Nb1-x%Sbx%O3 (abbreviated as NKL ... n both sides of the samples and fired at 570 degC.
294,10.1016/j.jeurceramsoc.2015.10.040,solid_state_ceramic_synthesis,"Li2Mg3BO6 (B = Ti, Sn, Zr) ceramics samples were p ... 6 h with a temperature-ramping rate of 4 degC/min."
295,10.1016/j.ijhydene.2012.09.015,solid_state_ceramic_synthesis,"The multiphase composite electrolytes were prepare ...  h, with heating and cooling rates of 1degC min-1."
296,10.1016/j.jpcs.2011.07.023,solid_state_ceramic_synthesis,"The polycrystalline samples of BNBT100x ceramics w ... measured by the Archimedes method, were above 94%."
297,10.1016/j.ssi.2014.11.011,solid_state_ceramic_synthesis,Ce0.9 - 0.9xGd0.1 - 0.1xNbxO2 - δ and Ce0.9 - 0.9x ... was between 94 and 97% of the theoretical density.
298,10.1007/s10854-012-0806-6,solid_state_ceramic_synthesis,Polycristalline samples of Bi1.7-xYxPb0.3Sr2Ca2Cu3 ...  start the formation of the superconducting phase.
299,10.1111/ijac.12573,solid_state_ceramic_synthesis,"Ti1-xDyxO2 with x = 0.10 and 0.20 powders were pre ... ere sintered at 870degC and 950degC, respectively."
300,10.1016/j.jeurceramsoc.2005.09.051,solid_state_ceramic_synthesis,The powders were prepared by conventional mixed ox ... pecimens was determined by the Archimedes' method.
301,10.1016/j.jeurceramsoc.2006.11.010,solid_state_ceramic_synthesis,"Samples were prepared by conventional mixed oxide  ... d samples were also cooled at 60, 15 and 5 degC/h."
302,10.1016/j.jpowsour.2014.09.082,solid_state_ceramic_synthesis,The LiCrO2 samples were prepared by solid state re ... ing ball milled LiCrO2 in Ar at 800 degC for 12 h.
303,10.1016/j.physb.2012.04.035,solid_state_ceramic_synthesis,"The samples were prepared using the solid-state re ... gC for 24 h under oxygen atmosphere, respectively."
304,10.1016/j.jeurceramsoc.2014.03.026,solid_state_ceramic_synthesis,Samples of the Ca5Co4(VO4)6 ceramics was synthesiz ... ated in air at 500 degC to remove the binder away.
305,10.1007/s10854-016-5647-2,solid_state_ceramic_synthesis,(1 - x)(0.948K0.5Na0.5NbO3 - 0.052LiSbO3) - xBi2O3 ... eramics were sintered at 1110 degC for 2 h in air.
306,10.1016/j.ssc.2008.06.021,solid_state_ceramic_synthesis,Ceramic samples were synthesized using the convent ... tively) were sintered at 1350 [?]C for 4 h in air.
307,10.1016/j.jeurceramsoc.2015.09.043,solid_state_ceramic_synthesis,The (Bi1/2Na1/2)0.935Ba0.065Ti1-x(Fe1/2Nb1/2)xO3 ( ... into preprepared powder with the same composition.
308,10.1016/j.electacta.2007.12.020,solid_state_ceramic_synthesis,"The composite oxides BaCe0.85-xZrxY0.15O3-δ (BCZY, ... nd the mean particle size were both close to 1 μm."
309,10.1007/s10854-015-4053-5,solid_state_ceramic_synthesis,Conventional processing of ceramic materials mostl ... nd ground well for other characterization studies.
310,10.1016/j.matlet.2011.08.038,solid_state_ceramic_synthesis,"Reagent-grade powders of PbO, NiO, Nb2O5, ZrO2, Ti ... pplying a DC electric field of 2 kV/mm for 30 min."
311,10.1016/j.jeurceramsoc.2013.11.039,solid_state_ceramic_synthesis,The (Ba0.4Sr0.6)TiO3 polycrystalline ceramics were ... -on silver electrodes for electrical measurements.
312,10.1007/s10854-014-2020-1,solid_state_ceramic_synthesis,"Sample of (Mg0.97Zn0.03)2(Ti0.95Sn0.05)O4 and CaTi ... t temperatures of 1,330-1,450 degC for 4 h in air."
313,10.1016/j.jeurceramsoc.2016.03.009,solid_state_ceramic_synthesis,The ZnNb2O6 pellets used for dielectric measuremen ... 0 degC in air for 2 h followed by furnace cooling.
314,10.1016/j.matlet.2006.05.005,solid_state_ceramic_synthesis,A PST target was made by conventional solid-state  ...  The sintered target appeared yellowish in colour.
315,10.1016/j.jeurceramsoc.2009.05.050,solid_state_ceramic_synthesis,NKN and Mn-doped NKN ceramics were prepared by a c ... he molded rods were sintered at 1100 degC for 2 h.
316,10.1016/j.solidstatesciences.2012.07.019,solid_state_ceramic_synthesis,The Zn0.5Ti1-xZrxNbO4 ceramics were prepared by th ... bO4 ceramics in this paper were higher than 96.7%.
317,10.1016/j.jallcom.2006.10.122,solid_state_ceramic_synthesis,Y-type hexagonal ferrites of composition Ba2-xBixZ ... 0-950 degC for 4 h and then cooled in the furnace.
318,10.1007/s10854-011-0548-x,solid_state_ceramic_synthesis,The (1 - x)Ba0.8Sr0.2TiO3-xCoFe2O4 ceramic composi ... e discs were sintered at 1300 degC for 2 h in air.
319,10.1016/j.jeurceramsoc.2007.08.011,solid_state_ceramic_synthesis,A conventional mixed oxide route was utilized to p ... 00 degC for 1-4 h at a heating rate of 300 degC/h.
320,10.1007/s10854-012-0742-5,solid_state_ceramic_synthesis,"BMT-0.38PT-xLN (x = 0.0-0.06) ceramics were synthe ... oss of PbO, Bi2O3and Li2CO3 caused by sublimation."
321,10.1016/j.matlet.2012.08.079,solid_state_ceramic_synthesis,LaFeO3 ceramic samples were synthesized by the con ... purity phase of Fe2O3 and the pores in the sample.
322,10.1007/s10854-008-9655-8,solid_state_ceramic_synthesis,Analytical reagent grade powders (purity 99.5%) of ... cooled to the room temperature along with furnace.
323,10.1016/j.jallcom.2014.10.122,solid_state_ceramic_synthesis,The Ce0.9Gd0.1O1.95 was prepared by a conventional ...  to obtain smooth and parallel surface conditions.
324,10.1007/s10853-014-8294-0,solid_state_ceramic_synthesis,Sample of MgTiO3 and CaTiO3 was separately synthes ...  at temperatures of 1210-1330 degC for 4 h in air.
325,10.1016/j.snb.2016.01.106,solid_state_ceramic_synthesis,Apatite-type lanthanum silicates solid electrolyte ... 600 degC for 5 h to form the dense bulk materials.
326,10.1016/j.jeurceramsoc.2009.04.030,solid_state_ceramic_synthesis,(1 - x)Li2TiO3-xMgO (0 <= x <= 0.5) ceramic sample ... were muffled with powders of the same composition.
327,10.1007/s10854-016-4762-4,solid_state_ceramic_synthesis,The raw materials were synthesized by conventional ... rious temperatures from 1180 to 1280 degC for 5 h.
328,10.1016/j.mseb.2006.08.034,solid_state_ceramic_synthesis,"Samples of SrBi2(Nb1-χTaχ)2O9 (χ = 0, 0.1, 0.3, 0. ... r electric field of about 8-10 kV/mm for 5-15 min."
329,10.1007/s10853-006-0161-1,solid_state_ceramic_synthesis,Strontium-doped lanthanum chromite powders were sy ... te of 2 degC/min in air and a holding time of 3 h.
330,10.1016/j.jmmm.2008.01.005,solid_state_ceramic_synthesis,Ni0.64Zn0.36Fe2O4 powder was synthesized via the c ... quartz tube and then sintered at 900 degC for 1 h.
331,10.1016/j.ssc.2015.01.001,solid_state_ceramic_synthesis,Bulk barium strontium titanate was prepared by sol ... disks were then heated at 1000 degC and 1400 degC.
332,10.1016/j.jallcom.2015.02.093,solid_state_ceramic_synthesis,Ba0.85Ca0.15Ti0.90Zr0.10O3-x wt% ZnO (BCZT-xZn) pi ... vinyl alcohol (PVA) binder at 650 degC for 30 min.
333,10.1007/s10854-011-0597-1,solid_state_ceramic_synthesis,"The general formula of the materials studied was 7 ... degC/min, then furnace cooled to room temperature."
334,10.1007/s10854-011-0551-2,solid_state_ceramic_synthesis,"A series of K0.5Na0.5NbO3-x ZnO (x = 0, 1, 2, 3 mo ...  disks were sintered in air at 1,100 degC for 2 h."
335,10.1016/j.physb.2007.01.001,solid_state_ceramic_synthesis,The ME composites having a general formula (x)BaTi ... s were prepared in ferroelectric-rich regions [8].
336,10.1016/j.jallcom.2012.11.155,solid_state_ceramic_synthesis,"In this study, Ag doped NKN-LT ceramics were fabri ... 0 degC at heating and cooling rates of 5 degC/min."
337,10.1016/j.materresbull.2014.07.002,solid_state_ceramic_synthesis,"Aurivillius type Bi4Ti3-xWx/2Nbx/2O12 (abbreviated ... 000-1120 degC for 2 h, depending on the x content."
338,10.1016/j.ceramint.2008.11.027,solid_state_ceramic_synthesis,Chromium-substituted lithium ferrites (Li0.5Fe2.5- ... ed at 1200 degC for 4 h in air and furnace cooled.
339,10.1016/j.jeurceramsoc.2009.06.001,solid_state_ceramic_synthesis,Y2W3O12 powders were prepared by solid-state react ... K/min to fabricate ZrSiO4/Y2W3O12 sintered bodies.
340,10.1002/celc.201500157,solid_state_ceramic_synthesis,The syntheses of SCT5-SCT40 were performed by usin ... d well and sintered at 1200 degC for another 10 h.
341,10.1016/j.matchemphys.2009.01.019,solid_state_ceramic_synthesis,The precursor NdSr2Cu2O6-δ was also prepared by th ... tered at 1050 degC for 24 h in flowing oxygen gas.
342,10.1007/s10854-016-5932-0,solid_state_ceramic_synthesis,The CTN ceramics were prepared by the conventional ... dopted to treat calcined powders after re-milling.
343,10.1016/j.mseb.2010.08.009,solid_state_ceramic_synthesis,The Zn(Ti1-xSnx)Nb2O8 ceramics were prepared by th ... ntered from 1080 degC to 1120 degC for 6 h in air.
344,10.1016/j.jallcom.2015.12.150,solid_state_ceramic_synthesis,LSMO powders was synthesized by the solid state re ... 600 degC for 5 h to form the dense bulk materials.
345,10.1016/j.jallcom.2011.03.077,solid_state_ceramic_synthesis,"Barium titanate composites with 0, 4, 6, 8, 10, 15 ... , all the pellets were covered in Al2O3 crucibles."
346,10.1007/s10854-015-3414-4,solid_state_ceramic_synthesis,Samples of the CaV2O6 ceramic was synthesized by t ...  for 4 h in air with a heating rate of 5 degC/min.
347,10.1016/j.matlet.2011.06.043,solid_state_ceramic_synthesis,La2(ZrxCe1 - x)2O7 oxides were prepared for this s ...  1600 degC for 2 h and subsequently cooled in air.
348,10.1016/j.sna.2009.12.027,solid_state_ceramic_synthesis,"The Bi0.5(Na0.78K0.22)0.5(Ti1-xZrx)O3 (x = 0.0, 0. ...  disks were embedded in the corresponding powders."
349,10.1016/j.jeurceramsoc.2014.01.040,solid_state_ceramic_synthesis,The xBi(Mg0.5Ti0.5)O3-(0.75 - x)PbTiO3-0.25(Bi0.5N ... of 4 kV/mm at 120 degC for 15 min in silicone oil.
350,10.1016/j.solidstatesciences.2011.08.001,solid_state_ceramic_synthesis,(1 - y)BiFe1-xScxO3-yBaTiO3 (y = 0.1-0.3; x = 0-0. ... oding with a post fire silver paste on both sides.
351,10.1007/s12034-015-1041-6,solid_state_ceramic_synthesis,"Briefly, 0.75BiFeO3-0.25Ba(Zr0.05Ti0.95)O3 (BF-BZT ... lets were then sintered in air at 990degC for 4 h."
352,10.1007/s10854-014-1901-7,solid_state_ceramic_synthesis,"The composition used in this research was Zn1-xNix ... 0-1,175 degC for 4 h in a sealed alumina crucible."
353,10.1016/j.jpcs.2013.01.026,solid_state_ceramic_synthesis,"The Yb2Ti2-xFexO7-δ (x=0.00, 0.05, 0.10, 0.15, 0.2 ... ls was performed to produce homogeneous materials."
354,10.1016/j.matchemphys.2016.02.017,solid_state_ceramic_synthesis,"Specimens with x = 0.05, 0.08, 0.1, 0.12, 0.15, 0. ... finally sintered at 1400-1480 degC for 4 h in air."
355,10.1016/j.jallcom.2008.07.112,solid_state_ceramic_synthesis,The NiCuZn and MgCuZn ferrites with the respective ... res from 850 degC to 950 degC in 25 degC interval.
356,10.1016/j.ssi.2007.08.006,solid_state_ceramic_synthesis,BaZr0.9Y0.1O3-δ (BZY10) powder was prepared by the ... henceforth known as the SB (sintered body)-sample.
357,10.1111/j.1551-2916.2010.04256.x,solid_state_ceramic_synthesis,A pseudo-ternary lead-free system (Na0.52K0.40)(Nb ... th by applying a dc field of 2-3 kV/mm for 15 min.
358,10.1007/s10854-009-0006-1,solid_state_ceramic_synthesis,Specimens of the LNT ceramics were prepared by a c ... 2.0 wt% BCu and then sintered at 900 degC for 2 h.
359,10.1016/j.jallcom.2010.11.106,solid_state_ceramic_synthesis,"Samples of Ba(Ti1-xSnx)O3 nanocrystalline powders, ...  wheel every 6 min after a rest interval of 2 min."
360,10.1016/j.jeurceramsoc.2014.09.003,solid_state_ceramic_synthesis,"(1 - x)BNTBT-xNN (x = 0, 0.01, 0.03, 0.05, 0.10, 0 ... , the pellets were embedded in self-source powder."
361,10.1016/j.apcata.2010.11.034,solid_state_ceramic_synthesis,The NiO-YSZ samples were synthesized using convent ... r and pestle and was calcined at 700 degC for 5 h.
362,10.1007/s10853-008-2572-7,solid_state_ceramic_synthesis,"Specimens of the LNT ceramics were prepared by con ...  were sintered at 1,050-1,150 degC for 2 h in air."
363,10.1016/j.matlet.2015.12.048,solid_state_ceramic_synthesis,The 0.5 mol% Er3+-doped (Ba0.97Ca0.03)(Sn0.06Ti0.9 ... r) which was sintered at 1430 degC for 2 h in air.
364,10.1007/s10854-014-2253-z,solid_state_ceramic_synthesis,"Calcium copper titanate, CaCu3Ti4O12 (CCTO) compou ... plied by Aldrich (99 %) were used as a comparison."
365,10.1007/s10854-016-6102-0,solid_state_ceramic_synthesis,Polycrystalline ferroelectric ceramics were prepar ... finally sintered between 900 and 960 degC for 2 h.
366,10.1111/j.1551-2916.2012.05128.x,solid_state_ceramic_synthesis,"High pure chemicals (>=99.9%, Alfa Aesar, Ward Hil ... intered at 1100degC for 2 h in ambient atmosphere."
367,10.1016/j.jeurceramsoc.2007.02.117,solid_state_ceramic_synthesis,LSCM powders were prepared by solid-state reaction ... s for 30 min and then fired at 1400 degC for 10 h.
368,10.1016/j.matlet.2012.04.049,solid_state_ceramic_synthesis,"Powder samples of Ca3 - xSi2O7: xDy3+ (x = 0.03, 0 ... es, the disk was ground to powder for measurement."
369,10.1007/s10854-012-0955-7,solid_state_ceramic_synthesis,"The samples used in this study were prepared by th ... amples were sintered at 1,260 degC for 6 h in air."
370,10.1016/j.matlet.2013.01.075,solid_state_ceramic_synthesis,"Specimens of the Ba4LiNb3-xSbxO3 (BLNS, 0<=x<=3) c ... ts were sintered at 1380-1425 degC for 4 h in air."
371,10.1016/j.jeurceramsoc.2004.07.036,solid_state_ceramic_synthesis,Samples of Ca[Ti1-x(Mg1/3Nb2/3)x]O3 with x = 0.40- ... emperatures from 1350 to 1500 degC for 4 h in air.
372,10.1007/s10008-007-0367-4,solid_state_ceramic_synthesis,LiCoPO4 nanoparticles were synthesized from a stoi ... 300 rpm. The ball-to-powder weight ratio was 20:1.
373,10.1016/j.matlet.2015.01.123,solid_state_ceramic_synthesis,(1-x)(K0.5Na0.5)NbO3-xBi(Zn0.75W0.25)O3 [(1-x)KNN- ... anging from 1100 degC to 1150 degC for 2 h in air.
374,10.1007/s10854-008-9837-4,solid_state_ceramic_synthesis,"ZnO, TiO2 and MgCO3 powders with 99.9% purity were ...  temperature range of 890-950 degC for 2 h in air."
375,10.1007/s10854-016-4418-4,solid_state_ceramic_synthesis,"CaCu3Ti4O12 dielectric ceramic was prepared by con ... 7 mm dia, 2.5 mm thick pellets using graphite die."
376,10.1111/j.1551-2916.2006.00957.x,solid_state_ceramic_synthesis,Polycrystalline ceramic samples with a composition ... asurements were made of a fired-on platinum paste.
377,10.1016/j.actamat.2013.11.006,solid_state_ceramic_synthesis,"LSCF1982 powder was synthesized by the solid-state ... C in air for 10 h, and were then cut and polished."
378,10.1007/s10854-011-0501-z,solid_state_ceramic_synthesis,(1 - x)Nd(Mg0.4Zn0.1Sn0.5)O3-xCa0.8Sr0.2TiO3 ceram ... ing rate and cooling rate were set at 10 degC/min.
379,10.1007/s10854-014-1956-5,solid_state_ceramic_synthesis,Superconducting samples with chemical composition  ... n furnace up to room temperature after each cycle.
380,10.1007/s10854-016-5606-y,solid_state_ceramic_synthesis,The samples involved in this article were prepared ...  The heating rates of the samples were 5 degC/min.
381,10.1016/j.ssc.2005.03.053,solid_state_ceramic_synthesis,Ceramic specimens of various compositions of (1-x) ... s found to be less than a percent after sintering.
382,10.1016/j.jpowsour.2005.03.058,solid_state_ceramic_synthesis,"LiOH*H2O (Aldrich, >=98%), Fe2O3 (Aldrich, >=99%), ...  in the conventional solid-state reaction process."
383,10.1007/s10854-016-4916-4,solid_state_ceramic_synthesis,The polycrystalline samples Eu0.5Sr0.5Mn1-xCrxO3 ( ... o room temperature to maximize the oxygen content.
384,10.1016/j.jpowsour.2010.12.071,solid_state_ceramic_synthesis,"The YBaCo2-xFexO5+δ (YBCF, x = 0.0, 0.2, 0.4 and 0 ... ared by the glycine nitrate process [41] and [42]."
385,10.1016/j.ssc.2010.06.001,solid_state_ceramic_synthesis,Specimens with nominal composition (Bi1.8Pb0.4Sr2C ... ooled at a rate of 2 degC/min to room temperature.
386,10.1111/j.1551-2916.2009.03561.x,solid_state_ceramic_synthesis,Specimens of the Ba4ZnTi11O27 ceramic were prepare ...  were sintered at 1150deg-1250degC for 2 h in air.
387,10.1016/j.jpowsour.2013.05.198,solid_state_ceramic_synthesis,Sr2Mg(Mo0.8Nb0.2)O6-δ oxide was synthesized by sol ... tion at 900 degC under flowing 10% H2/N2 for 50 h.
388,10.1016/j.jeurceramsoc.2016.02.015,solid_state_ceramic_synthesis,The TiO2 ceramics were prepared using conventional ... gC for 4 h in air at a heating rate of 5 degC/min.
389,10.1016/j.ssi.2012.10.008,solid_state_ceramic_synthesis,"The Zr1 - xMgxP2O7 (x = 0.00, 0.03, 0.06, 0.09, an ...  300 MPa and sintered at 1250 degC in air for 5 h."
390,10.1016/j.jeurceramsoc.2013.08.041,solid_state_ceramic_synthesis,MDLS powder with a composition of La9.8Si5.7Mg0.3O ... brication of both MDLS paste and anode substrates.
391,10.1016/j.jpowsour.2014.03.070,solid_state_ceramic_synthesis,All the samples were prepared via the conventional ...  some protective powder with the same composition.
392,10.1016/j.jallcom.2014.06.144,solid_state_ceramic_synthesis,Series of 0.09PSN-0.09PZN-xPZ-(0.82 - x)PT + y mol ... d in a covered crucible at 1100-1270 degC for 3 h.
393,10.1016/j.matlet.2015.07.106,solid_state_ceramic_synthesis,"Ceramic samples were prepared using the solid-stat ... 2O3 were named S0, S2, S4, S6 and S8 respectively."
394,10.1016/j.jallcom.2010.04.234,solid_state_ceramic_synthesis,"(0.94 - x)NKN-xBN-LS6 (x = 0.002, 0.004, 0.006, 0. ... he green disks were sintered at 1105 degC for 2 h."
395,10.1016/j.jeurceramsoc.2005.03.137,solid_state_ceramic_synthesis,Ceramic samples were prepared by conventional mixe ... ntering was performed in air at 1500 degC for 5 h.
396,10.1016/j.matlet.2006.07.141,solid_state_ceramic_synthesis,The polycrystalline ceramic compounds in the BaO-T ... measured in kerosene using the Archimedes' method.
397,10.1016/j.mseb.2004.04.003,solid_state_ceramic_synthesis,"(Ba1-xCax)TiO3 (x=0.1, 0.3, 0.5,0.7 and 0.9) ceram ...  min-1, the ceramics were cooled with the furnace."
398,10.1016/j.jpowsour.2011.05.046,solid_state_ceramic_synthesis,The carbon-shell coated LiFePO4 was synthesized us ... nitrogen-argon mixture to get LiFePO4/C composite.
399,10.1016/j.matdes.2015.12.149,solid_state_ceramic_synthesis,Zr1.95Ca0.05O3.95 solid solution was prepared thro ... overed with the raw powders to avoid lithium loss.
400,10.1016/j.jeurceramsoc.2005.09.065,solid_state_ceramic_synthesis,The Ba5Nb4O15 powders were synthesized by conventi ... 50 degC for 2 h with a heating rate of 5 degC/min.
401,10.1007/s10854-015-3340-5,solid_state_ceramic_synthesis,(1 - x)K0.5Na0.5NbO3-xEuTiO3 ceramics with x = 0.0 ... crucibles in static air at 1050-1110 degC for 2 h.
402,10.1016/j.jmmm.2010.07.043,solid_state_ceramic_synthesis,"Polycrystalline samples of x=0.7, 0.75 and 0.9, xB ... der (rhombohedral phase) as summarised in Table 1."
403,10.1016/j.matlet.2003.09.056,solid_state_ceramic_synthesis,Microwave dielectric ceramics of Ba[(Zn1-xCox)1/3N ... ed at temperatures from 1350 to 1450 degC for 4 h.
404,10.1007/s10854-014-2329-9,solid_state_ceramic_synthesis,"MnO2-doped BF69-BMT2-BT29 ceramics with x = 0.20 a ... a closed alumina crucible, then cooling with oven."
405,10.1007/s10854-014-2555-1,solid_state_ceramic_synthesis,"(1 - x)BT-xBZW (0 <= x <= 0.2) ceramics were prepa ... , ranging from 1,250 to 1,410 degC for 2 h in air."
406,10.1016/j.ceramint.2003.12.081,solid_state_ceramic_synthesis,"The starting materials were Bi2O3, ZnO, Ta2O5 and  ... mined by the Archimedes' method (buoyancy method)."
407,10.1016/j.jpowsour.2013.06.155,solid_state_ceramic_synthesis,Ceramic membranes of Sr0.9Y0.1ZrO3-δ were prepared ... 90 MPa followed by sintering at 1500 degC for 6 h.
408,10.1016/j.mseb.2010.06.011,solid_state_ceramic_synthesis,The RE/Ni doped Co0.6Zn0.4Fe2O4 ferrites were synt ... ng was done at 1523 K for 9 h in a muffle furnace.
409,10.1016/j.jallcom.2008.12.081,solid_state_ceramic_synthesis,The LiMn2O4 powder was prepared by a solid-state r ... 0 degC for 72 h in air with intermittent grinding.
410,10.1016/j.matlet.2012.05.008,solid_state_ceramic_synthesis,"The phosphors La3 - xNbO7:xEu3+ (x = 0.05, 0.10, 0 ... homogeneous mixture was calcined at 1400 degC/6 h."
411,10.1016/j.optmat.2015.05.021,solid_state_ceramic_synthesis,"The samples were prepared by a high temperature so ... lly, the as-prepared powder samples were obtained."
412,10.1016/j.ssc.2007.11.024,solid_state_ceramic_synthesis,La1.85Sr0.15CuO4 samples were prepared by a cerami ... ples were cooled to room temperature in a furnace.
413,10.1016/j.elecom.2007.05.034,solid_state_ceramic_synthesis,The spinel LiMn2O4 powders were prepared by a soli ... 0 degC in air for 72 h with intermittent grinding.
414,10.1007/s10854-009-9933-0,solid_state_ceramic_synthesis,Ceramic specimens were fabricated by conventional  ... C for 1 h at a heating/cooling rate of 180 degC/h.
415,10.1111/j.1551-2916.2005.00794.x,solid_state_ceramic_synthesis,(1-x)Al0.5Ta0.5O2-xMg0.33Ta0.67O2 powder compositi ... hieve a ratio of thickness to diameter of 0.4-0.5.
416,10.1016/j.jpcs.2011.07.004,solid_state_ceramic_synthesis,BaTi1-x(Al1/2Nb1/2)xO3 ceramics were prepared thro ... der and then sintered at 1400 degC for 5 h in air.
417,10.1111/j.1551-2916.2008.02672.x,solid_state_ceramic_synthesis,The starting materials used were high-purity (>99. ... mperatures from 900deg to 1000degC for 4 h in air.
418,10.1016/j.ssi.2003.10.008,solid_state_ceramic_synthesis,Stoichiometric mixtures of Bi2O3 and CuO powder (r ... ermediate regrindings in a planetary mill for 1 h.
419,10.1016/j.apsusc.2006.06.006,solid_state_ceramic_synthesis,Ceramic materials based on the ZrO2-SnO2-TiO2 tern ... ssing and then sintered at 1230-1325 degC for 2 h.
420,10.1016/j.matlet.2011.09.113,solid_state_ceramic_synthesis,The Bi5FeTi3O15 ceramics were prepared by the soli ... f 30 MPa and sintered at 1000 degC for 4 h in air.
421,10.1016/j.jpcs.2011.12.024,solid_state_ceramic_synthesis,CCTO powder was obtained from a solid-state reacti ...  contents were named as P0-P4 as shown in Table 1.
422,10.1016/j.solidstatesciences.2006.11.011,solid_state_ceramic_synthesis,"The selected ceramic was synthesised by solid stat ... ed. Their values were 0.16 and 0.96, respectively."
423,10.1016/j.ssi.2004.01.008,solid_state_ceramic_synthesis,A solid-state reaction procedure was adopted to pr ... Their density was measured with Archimedes method.
424,10.1111/j.1551-2916.2009.02931.x,solid_state_ceramic_synthesis,"(Ca1+xSm1-x)(Al1-xTix)O4 (x=0, 0.02, 0.06, 0.1, 0. ... /min and further cooled freely inside the furnace."
425,10.1016/j.scriptamat.2008.03.018,solid_state_ceramic_synthesis,Analytical reagent grade powders (purity 99.5%) of ... ples were then sintered at 1280-1300 degC for 1 h.
426,10.1016/j.jallcom.2006.04.065,solid_state_ceramic_synthesis,All Zn1-xTixO (0 <= x <= 0.05) samples were fabric ... at 1673 K for 20 h in air and then furnace cooled.
427,10.1007/s10854-015-3362-z,solid_state_ceramic_synthesis,The solid-state reaction technique was used to pre ... m the electrodes for electrical characterizations.
428,10.1007/s10008-016-3197-4,solid_state_ceramic_synthesis,Spinel LiMn2O4 powder was prepared by a solid-stat ...  respectively. The hearting rate was 3 degC min-1.
429,10.1111/j.1744-7402.2010.02495.x,solid_state_ceramic_synthesis,Samples of (Mg1-xNix)2TiO4 were synthesized using  ... ets were sintered at 1350-1475degC for 4 h in air.
430,10.1016/j.matchemphys.2007.01.004,solid_state_ceramic_synthesis,The NiCuZn ferrite specimens were prepared by the  ... side the electric furnace to the room temperature.
431,10.1016/j.jallcom.2014.10.056,solid_state_ceramic_synthesis,The starting materials used were high-purity (>99% ... disks and sintered at 875 degC for 4 h afterwards.
432,10.1016/j.ssi.2015.11.016,solid_state_ceramic_synthesis,Ba0.5Sr0.5Co0.8Fe0.2O3 - δ composite oxide was syn ... mixed with 30 wt. % SDC to make composite cathode.
433,10.1016/j.matlet.2016.06.051,solid_state_ceramic_synthesis,(Pb0.87Ba0.08Sr0.02La0.02) (Zr0.65Sn0.27Ti0.08)O3  ... h surfaces of the specimens at 600 degC for 10 min
434,10.1016/j.ssi.2009.03.016,solid_state_ceramic_synthesis,"BaCe(0.9 - x)ZrxY0.1O(3 - δ) powders (x = 0, 0.3,  ... 350 MPa) and sintered in air at 1700 degC for 6 h."
435,10.1016/j.jpowsour.2010.08.043,solid_state_ceramic_synthesis,BaCe0.8Y0.15Nd0.05O3-δ (BCYN) perovskite powders w ... discs were polished and reduced to 1 mm thickness.
436,10.1016/j.physb.2009.08.064,solid_state_ceramic_synthesis,"Samples of compositions Ba (Ti1-xWx) O3; x=0.0, 0. ... e pellets were then sintered at 1250 degC for 2 h."
437,10.1016/j.actamat.2017.01.052,solid_state_ceramic_synthesis,The (1-x)Na0.5Bi0.5TiO3-xK0.5Bi0.5TiO3 ceramic sam ... n the synthesis procedure is given elsewhere [28].
438,10.1016/j.jeurceramsoc.2007.02.159,solid_state_ceramic_synthesis,"Five Ba1-xSrxTiO3 (x = 0, 0.1, 0.2, 0.3 and 0.4) p ... for 24 h, dried and calcined at 1150 degC for 5 h."
439,10.1111/j.1551-2916.2008.02742.x,solid_state_ceramic_synthesis,A (Mg1-xCox)2TiO4 sample was synthesized by a conv ...  were sintered at 1300deg-1450degC for 4 h in air.
440,10.1016/j.materresbull.2012.01.017,solid_state_ceramic_synthesis,[(Ba1-3x/2Bix)0.85Ca0.15](Ti0.90Zr0.10)O3 (BBCZT)  ... /mm at ~30 degC in a silicone oil bath for 30 min.
441,10.1016/j.matchemphys.2008.11.045,solid_state_ceramic_synthesis,"The Ba0.6Sr0.4TiO3 powder was first prepared by th ... , and 60 wt% content of BaZn6Ti6O19, respectively."
442,10.1016/j.mseb.2009.08.007,solid_state_ceramic_synthesis,The replacement mechanism of Li2TiO3-Li3NbO4 solid ...  were muffled with powder of the same composition.
443,10.1111/j.1551-2916.2006.01432.x,solid_state_ceramic_synthesis,Sample powders of BZN were prepared using a conven ...  in order to reduce the ZnO loss during sintering.
444,10.1007/s10854-016-5640-9,solid_state_ceramic_synthesis,Specimens were prepared through conventional solid ... emperature range of 1200-1300 degC for 3 h in air.
445,10.1016/j.ssi.2016.02.013,solid_state_ceramic_synthesis,Ba0.9Sr0.1Ce0.85Y0.15O3 - δ powders were prepared  ... 150 MPa and sintered at 1600 degC in air for 10 h.
446,10.1111/jace.12418,solid_state_ceramic_synthesis,"(Na0.5K0.5)xNbO3 + 0.5 mol% CT samples (NKxNCT), w ... egC for 2 h at a heating rate of 5degC/min in air."
447,10.1007/s10854-016-4596-0,solid_state_ceramic_synthesis,Ceramic specimens 0.6Bi0.5Na0.5TiO3-(0.4 - x)NaNbO ... position to minimize the evaporation of Na and Bi.
448,10.1016/j.jpcs.2010.10.084,solid_state_ceramic_synthesis,"Samples of composition SrCo1-xFexO3-δ (x=0.2, 0.4, ... imedes method using water as the immersion medium."
449,10.1016/j.electacta.2012.04.102,solid_state_ceramic_synthesis,SZCY-541 and SZY-91 were prepared by solid-state r ... pe into 0.5 mm in thickness and 13 mm in diameter.
450,10.1016/j.powtec.2012.10.002,solid_state_ceramic_synthesis,"Six polycrystalline samples (x = 0.0, 0.1, 0.2, 0. ... then were cooled in a furnace at room temperature."
451,10.1016/j.matlet.2016.05.081,solid_state_ceramic_synthesis,"Bi0.95La0.05Fe1-xCoxO3 (x=0, 0.1 and 0.2) ceramics ...  isothermally for 30 min under 5 GPa at 1000 degC."
452,10.1016/j.matlet.2014.11.060,solid_state_ceramic_synthesis,(1-x)BFO-xYCO (0<=x<=0.3) ceramics were prepared b ... d isothermally for 30 min under 4 GPa at 950 degC.
453,10.1016/j.jpowsour.2007.07.076,solid_state_ceramic_synthesis,"Solid phase synthesis (SPS): Composition LSCF6428  ... C, then remilled for 10 h and sieved (400 meshes)."
454,10.1007/s10853-010-5080-5,solid_state_ceramic_synthesis,The ceramics with the composition of (K0.4425Na0.5 ...  the distance between the two surfaces of the bar.
455,10.1016/j.mseb.2006.01.018,solid_state_ceramic_synthesis,Samples of Na(Co1-y-zCuyNiz)2O4 (0 <= y <= 0.15 an ... at 1203 K for 12 h in air and then furnace cooled.
456,10.1016/j.actamat.2011.10.030,solid_state_ceramic_synthesis,"The samples, formulated as [(ZrO2)1-x(CeO2)x]0.92( ... Pa and then sintered at 1500 degC for 10 h in air."
457,10.1111/j.1744-7402.2009.02379.x,solid_state_ceramic_synthesis,Samples of BaTiSiO5 were prepared using convention ...  between 900degC and 1220degC for a period of 2 h.
458,10.1016/j.jallcom.2009.06.035,solid_state_ceramic_synthesis,Sample of (Mg0.95Co0.05)2TiO4 and SrTiO3 were sepa ... and the cooling rate were both set at 10 degC/min.
459,10.1111/j.1551-2916.2009.03204.x,solid_state_ceramic_synthesis,"To synthesize BaCe0.5Zr0.3Y0.2-xZnxO2.9-0.5x (0<x< ... , and then sintered at 1300degC for 2-10 h in air."
460,10.1111/j.1551-2916.2007.01918.x,solid_state_ceramic_synthesis,NBT+x wt% Er2O3 (x from 0 to 3) ceramics (NBT-xEr) ... on oil bath at 120degC under 5.0 kV/mm for 30 min.
461,10.1016/j.matlet.2003.09.049,solid_state_ceramic_synthesis,Y-type hexagonal ferrite powders were prepared by  ... 150 degC for 4 h in air and cooled in the furnace.
462,10.1007/s10853-013-7183-2,solid_state_ceramic_synthesis,MnZn-ferrites of the cubic spinel structure having ...  uniaxial compaction at pressures of ~500 kgf/cm2.
463,10.1016/j.mseb.2015.01.003,solid_state_ceramic_synthesis,"Samples with compositions Mg1+δTiO3+δ (δ = 0, 0.05 ... quently sintered at 1200-1400 degC for 3 h in air."
464,10.1007/s10854-016-4658-3,solid_state_ceramic_synthesis,"High purity oxides Bi2O3, TiO2, Na2CO3 and MgO fro ... pellets are above 97 % of the theoretical density."
465,10.1007/s10854-014-2185-7,solid_state_ceramic_synthesis,"The samples of BSNT + xTiO2 + y wt% Al2O3(x = 0-2, ...  then sintered at 1,240-1,320 degC in air for 5 h."
466,10.1016/j.ceramint.2009.07.026,solid_state_ceramic_synthesis,"Ba4(La1-y-zSmyBiz)9.33Ti18O54, y = 0.7 and z = 0.0 ... for 2 h in air in a linearly programmable furnace."
467,10.1016/j.matlet.2004.07.060,solid_state_ceramic_synthesis,"Synthesis of (Ca1-xZnx)2P2O7 (x=0.1, 0.2, 0.3, 0.4 ... erature increased with the increase of Ca content."
468,10.1016/j.solidstatesciences.2011.08.019,solid_state_ceramic_synthesis,"Starting materials were Li2CO3 (""special purity 20 ... s prepared by hot pressing at 800 degC and 40 MPa."
469,10.1016/j.ssc.2005.09.035,solid_state_ceramic_synthesis,Polycrystalline SrLaCoO4 were prepared by a solid- ...  for 3 h. Silver paste was used as the electrodes.
470,10.1007/s10854-015-3075-3,solid_state_ceramic_synthesis,0.365BiScO3-0.635PbTiO3-xMnO2 ceramics (with MnO2  ... f the ceramics changed from light yellow to black.
471,10.1007/s10854-006-0003-6,solid_state_ceramic_synthesis,The polycrystalline Ba0.6Sr0.4CrxTi1-xO3 (x = 0.4- ...  MPa. The discs were sintered at 1440degC for 4 h.
472,10.1016/j.matlet.2004.04.027,solid_state_ceramic_synthesis,Samples of Sm(Co1/2Ti1/2)O3 were synthesized by co ... and the cooling rate were both set at 10 degC/min.
473,10.1007/s10853-013-7627-8,solid_state_ceramic_synthesis,The NBCTO powders were prepared by solid state rea ... n to obtain powder with particle sizes of ~2-4 μm.
474,10.1016/j.jallcom.2009.10.048,solid_state_ceramic_synthesis,Ca3Co4O9 (349) powder was synthesized by a convent ... axially (92 MPa) into pellets (25 mm in diameter).
475,10.1016/j.matlet.2014.03.002,solid_state_ceramic_synthesis,"Li2Mg(Ti1-xSnx)3O8 (x=0.10, 0.15, 0.2, and 0.25) c ... ckness, sintered at 1060-1140 degC for 4 h in air."
476,10.1016/j.ssi.2013.09.024,solid_state_ceramic_synthesis,LLZ was prepared by conventional solid state react ... red at 1180 degC for 36 h under an air atmosphere.
477,10.1111/j.1551-2916.2010.03657.x,solid_state_ceramic_synthesis,"Three compounds in the Sr4-mLamTim-1Ta4-mO12 (m=1, ... g-1620degC until the highest density was achieved."
478,10.1007/s10854-015-4152-3,solid_state_ceramic_synthesis,Conventional solid state reaction procedure was us ... the pellets were found using Archimedes principle.
479,10.1016/j.ssi.2014.10.028,solid_state_ceramic_synthesis,Polycrystalline Bi2VO5.5 ceramic was synthesised v ... r 24 h with heating and cooling rates of 50 Kh- 1.
480,10.1007/s10854-015-3094-0,solid_state_ceramic_synthesis,The produced materials Bi1/2Na1/2Ti1-x(Nd1/2Ta1/2) ... ed into prepared powder with the same composition.
481,10.1016/j.optmat.2006.01.032,solid_state_ceramic_synthesis,"The Nd:YSAG ceramic samples were fabricated by the ... % and thickness of 6.1, 6.1, 5.0 mm, respectively."
482,10.1007/s10854-014-2482-1,solid_state_ceramic_synthesis,"Ceramic samples of Ca2-xSrxBi4Ti5O18 with x = 0.0, ... r to sintering at 1,125-1,225 degC for 5 h in air."
483,10.1016/j.ssc.2016.08.001,solid_state_ceramic_synthesis,"High-purity (99.9%) oxides: α-Bi2O3, α-Fe2O3 and b ... in a resistive furnace at 1073 and 1173 K for 1 h."
484,10.1007/s10854-015-3155-4,solid_state_ceramic_synthesis,The samples involved in this study were synthesize ... ts were sintered at 1150-1275 degC for 4 h in air.
485,10.1016/j.matlet.2010.11.028,solid_state_ceramic_synthesis,(1 - x)CaWO4-xNa2W2O7 (0 <= x <= 0.04) samples wer ... t.% Ag) in ambient atmosphere at 875 degC for 2 h.
486,10.1016/j.tsf.2011.04.006,solid_state_ceramic_synthesis,"The PZT and BLT targets with compositions of PbZr0 ...  of 60 mm, and then sintered at 1100 degC for 3 h."
487,10.1016/j.jeurceramsoc.2004.10.005,solid_state_ceramic_synthesis,"PZN-PZT ceramics with the nominal composition Pb[( ... nation, and then isostatically pressed at 200 MPa."
488,10.1016/j.matlet.2013.05.085,solid_state_ceramic_synthesis,"BaTi1-x(Co0.5Nb0.5)xO3 ceramics, where x=0.2, 0.4  ... re sintered at various temperature for 5 h in air."
489,10.1016/j.ceramint.2013.01.115,solid_state_ceramic_synthesis,"In addition, ST powders were also prepared by soli ... calcination being conducted at 1400 degC for 10 h."
490,10.1007/s10854-014-2512-z,solid_state_ceramic_synthesis,"BCN ceramics were prepared with high-purity (99.9  ... were sintered at 1,300-1,460 degC for 12 h in air."
491,10.1016/j.matchemphys.2007.12.019,solid_state_ceramic_synthesis,Nd3+-doped barium titanate were fabricated accordi ... gC for 2 h and sintered at 1250-1400 degC for 3 h.
492,10.1016/j.jeurceramsoc.2012.05.024,solid_state_ceramic_synthesis,"Ceramic samples of Ca(1-x)Nd2x/3TiO3 with x = 0, 0 ... ample to prevent contamination from the substrate."
493,10.1007/s10854-015-4075-z,solid_state_ceramic_synthesis,Polycrystalline samples of Bi2Sr2-xVxCa1Cu1.75Na0. ...  order to reach a large amount of pure 2212-BSCCO.
494,10.1007/s10853-015-9715-4,solid_state_ceramic_synthesis,"Bao.8La0.2Co0.88-xFexNb0.12O3-δ (BLCFN, x = 0, 0.1 ... BLCFN-0.2, BLCFN-0.3, and BLCFN-0.5, respectively."
495,10.1016/j.jeurceramsoc.2008.04.021,solid_state_ceramic_synthesis,Ba2Ti3Nb4O18 were prepared by the conventional sol ...  for 2 h with 5 degC/min heating and cooling rate.
496,10.1016/j.elecom.2003.08.019,solid_state_ceramic_synthesis,Starting materials for preparing LiMn2-xAlxO4 (0.0 ... ing at 600 degC (MA600) instead of rotary heating.
497,10.1007/s10854-012-0958-4,solid_state_ceramic_synthesis,A series of 0.998 [0.95(K0.5Na0.5)NbO3-0.05LiSbO3] ...  80 degC for 15 min under a dc field of 3.5 kv/mm.
498,10.1002/chem.201404476,solid_state_ceramic_synthesis,The LiFeO2-LiAlO2 composite material was prepared  ... for conductivity and electrochemical measurements.
499,10.1111/j.1551-2916.2008.02676.x,solid_state_ceramic_synthesis,"0.7BiFe1-xCrxO3-0.3BaTiO3(BFOCx-BT, with x=0-0.2)  ... troded with a postfire silver paste on both sides."
500,10.1111/j.1551-2916.2012.05192.x,solid_state_ceramic_synthesis,The Zn3B2O6 ceramics were prepared by conventional ... s were sintered at 875degC-975degC for 4 h in air.
501,10.1016/j.physc.2007.03.398,solid_state_ceramic_synthesis,A bulk target of LCO was prepared by the conventio ... rom the powder and sintered at 1150 degC for 20 h.
502,10.1016/j.ceramint.2003.12.111,solid_state_ceramic_synthesis,All the samples were prepared by conventional soli ... sintering temperature ranged from 950 to 980 degC.
503,10.1007/s10854-007-9477-0,solid_state_ceramic_synthesis,MnNb2O6 compound was prepared using the convention ... egC for 2 h and single phase MnNb2O6 was obtained.
504,10.1016/j.jct.2016.05.009,solid_state_ceramic_synthesis,We prepared Bi12.5Nd1.4In0.1ReO24.5 phase by solid ... 12.5Nd1.4In0.1ReO24.5 became a phase pure ceramic.
505,10.1016/j.elecom.2006.03.034,solid_state_ceramic_synthesis,La0.8Sr0.2Ga0.8Mg0.15Co0.05O3 electrolyte was prep ... ered disks were polished to a thickness of 0.3 mm.
506,10.1016/j.ijhydene.2014.05.150,solid_state_ceramic_synthesis,"To compare with SCFT, the SrCo0.8Fe0.2O3-δ (SCF) s ... 50 degC, 1000 degC, and 1200 degC for 10 h in air."
507,10.1016/j.jssc.2007.09.027,solid_state_ceramic_synthesis,The nominal BaZr0.8Y0.2O3-δ powder was prepared by ... id-state reaction and fired at 1325 degC for 10 h.
508,10.1016/j.mseb.2009.08.014,solid_state_ceramic_synthesis,"All samples in this study were prepared from high- ... g rate of 3 degC/min, and cooled with the furnace."
509,10.1007/s10854-015-4168-8,solid_state_ceramic_synthesis,"In this paper, Y2.94(Al1-xGax)5O12:0.06Ce phosphor ... e is 0.15, 0.2, 0.25, 0.3 and 0.35, respectively)."
510,10.1007/s10854-015-2978-3,solid_state_ceramic_synthesis,BSCN ceramics were prepared with high-purity (99.9 ... s were sintered at 1340-1460 degC for 12 h in air.
511,10.1016/j.jeurceramsoc.2012.03.025,solid_state_ceramic_synthesis,"Sample powders of Ba3(Mg1-xCox)Nb2O9 (for x = 0, 0 ...  and all ceramics has >95% of theoretical density."
512,10.1016/j.jallcom.2013.08.159,solid_state_ceramic_synthesis,Polycrystalline BiFeO3 and doped Bi0.95Pr0.05FeO3  ... ain high density and better dielectric properties.
513,10.1007/s10854-014-2408-y,solid_state_ceramic_synthesis,"High-purity CaCO3, SrCO3, Li2CO3, TiO2, Ba (OH)2.  ... ed at temperatures of 1,230-1,300 degC/4 h in air."
514,10.1007/s10853-006-0367-2,solid_state_ceramic_synthesis,"Commercial purity powders including PbO (>99.5%),  ... d powder and PbZrO3 + ZrO2 (10 wt%) mixing powder."
515,10.1007/s10854-013-1358-0,solid_state_ceramic_synthesis,"Barium zirconium titanate (BZT) ceramic powder was ... d at 1,100 degC for 4 h by a programmable furnace."
516,10.1016/j.jeurceramsoc.2016.06.022,solid_state_ceramic_synthesis,"Analytical-grade powders: Na2CO3(99.8%), K2CO3(99% ...  150 MPa and sintered at 1180 degC for 3 h in air."
517,10.1111/j.1551-2916.2012.05428.x,solid_state_ceramic_synthesis,"On the other hand, Pb(Zr0.52Ti0.48)O3 powders were ... e as-prepared pellets were studied for comparison."
518,10.1002/aelm.201400051,solid_state_ceramic_synthesis,Materials and Synthesis: The ceramic samples of PT ...  procedure we refer to the Supporting Information.
519,10.1007/s10854-015-4219-1,solid_state_ceramic_synthesis,Specimens were prepared through conventional solid ...  in a temperature range of 1200-1300 degC for 3 h.
520,10.1016/j.ceramint.2003.12.006,solid_state_ceramic_synthesis,The samples with chemical formula of Bi1.5ZnNNb2.5 ...  into powder for crystal structural investigation.
521,10.1007/s10854-015-3120-2,solid_state_ceramic_synthesis,The Sr1-xCaxNa0.5Bi4.5Ti5O18 + 1 wt% CeO2 (SCxNBTC ... ired at 740 degC for 20 min to form the electrode.
522,10.1016/j.matchemphys.2007.10.025,solid_state_ceramic_synthesis,The ZnO/PZT composites were prepared by the conven ... ere about 10 mm in diameter and 1 mm in thickness.
523,10.1007/s10854-007-9135-6,solid_state_ceramic_synthesis,The composites were prepared by standard ceramic m ... C for 12 h and furnace cooled to room temperature.
524,10.1016/j.jallcom.2009.11.083,solid_state_ceramic_synthesis,Conventional solid-state reaction was used to prep ... nder a direct current field of 6 kV/mm for 20 min.
525,10.1016/j.jmmm.2010.02.025,solid_state_ceramic_synthesis,"YIG:Bi ferrite powders, having stoichiometric comp ... e characterized and used as the reference samples."
526,10.1016/j.jpowsour.2007.08.026,solid_state_ceramic_synthesis,"The (BaO)0.11(Bi2O3)0.89 powders were prepared by  ... irconia balls and C2H5OH for 24 h, and then dried."
527,10.1016/j.matlet.2007.03.027,solid_state_ceramic_synthesis,LiFePO4 sample was prepared by a solid state react ... o for Li:Fe:P was 0.98:1:1 for the LiFePO4 sample.
528,10.1016/j.jpowsour.2006.12.090,solid_state_ceramic_synthesis,"La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM8282), La0.8Sr0.2Ga0 ... ls were identified using XRD (Panalytical X'pert)."
529,10.1016/j.jpowsour.2010.12.099,solid_state_ceramic_synthesis,"La0.8Sr0.2MnO3 (LSM20) powder was synthesized usin ... aser particle analyzer (Malvern, Mastersizer2000)."
530,10.1016/j.apsusc.2007.06.004,solid_state_ceramic_synthesis,A titanium-doped In2O3 (TIO) target was prepared b ... trict our study to this composition in this paper.
531,10.1007/s10854-008-9774-2,solid_state_ceramic_synthesis,"BZT ceramic targets were prepared by a conventiona ... s were then sintered at 1,340 degC for 2 h in air."
532,10.1016/j.jeurceramsoc.2006.05.023,solid_state_ceramic_synthesis,Ceramics with molar formula Ba(Zn1/3Ta2/3)O3 were  ... was carried out at T = 1150 degC in air for 2.5 h.
533,10.1007/s10853-014-8769-z,solid_state_ceramic_synthesis,PbTiO3 was prepared through solid state reaction m ... d for the synthesis of magnetoelectric composites.
534,10.1007/s10854-011-0578-4,solid_state_ceramic_synthesis,"In this work, Na1/2Y1/2Cu3Ti4O12 was prepared by t ... these pellets were sintered at 1,090 degC for 5 h."
535,10.1016/j.ssi.2004.08.010,solid_state_ceramic_synthesis,LSGM specimens (x=0 and 0.1) have been prepared by ... and finally sintered in air at 1470 degC for 24 h.
536,10.1007/s00339-012-7443-z,solid_state_ceramic_synthesis,Ball milling is a mechanical method. In this metho ... d at 950 degC for 12 h for dielectric measurement.
537,10.1007/s10853-007-1641-7,solid_state_ceramic_synthesis,"Bi1-xGdxNbO4 ceramics samples (x = 0.003, 0.005, 0 ... eratures from 850 degC to 920 degC in air for 3 h."
538,10.1007/s10854-014-2397-x,solid_state_ceramic_synthesis,The BMN ceramic target was prepared by conventiona ... d cooled down to room temperature with 3 degC/min.
539,10.1016/j.matlet.2015.04.021,solid_state_ceramic_synthesis,CaTi1-x(Nb0.5Ga0.5)xO3 (x=0.2-0.8) compositions we ... ils and sintered at 1325-1475 degC for 4 h in air.
540,10.1016/j.jallcom.2015.08.222,solid_state_ceramic_synthesis,Ceramics with nominal compositions of K0.5Na0.5NbO ... omposition and sintered at 1060-1100 degC for 2 h.
541,10.1016/j.ijhydene.2016.04.210,solid_state_ceramic_synthesis,"The co-doped La10Si5Al1-xMxO27-δ (M = W, In, Nb or ...  calculated from the values of lattice parameters."
542,10.1002/celc.201402143,solid_state_ceramic_synthesis,SSNC was synthesized via a solid-state reaction us ... degC in air for 40 h to form the perovskite oxide.
543,10.1016/j.matlet.2013.09.069,solid_state_ceramic_synthesis,The composition used in this research was Ni0.5-xZ ...  at a temperature range of 1075-1150 degC for 4 h.
544,10.1016/j.jeurceramsoc.2006.11.030,solid_state_ceramic_synthesis,"The Ba5+nTinNb4O15+3n (n = 0.3, 0.5, 0.6, 0.7, 0.9 ... ed samples were measured by the Archimedes method."
545,10.1016/j.jpowsour.2008.01.023,solid_state_ceramic_synthesis,Non-precalcined powders were prepared by a simple  ...  pores with different grain sizes were eliminated.
546,10.1007/s10854-013-1624-1,solid_state_ceramic_synthesis,"The conventional solid-state method has been emplo ... 350-1,450 degC for 6 h under oxidizing atmosphere."
547,10.1016/j.jpowsour.2009.01.020,solid_state_ceramic_synthesis,BaZr0.85Y0.15O3-δ ceramic powder was synthesized b ... ach were more than 95% of the theoretical density.
548,10.1016/j.elecom.2009.02.007,solid_state_ceramic_synthesis,A-site deficient (La0.8Sr0.2)0.95MnO3 (LSM95) powd ... degC and pure perovskite phase LSM95 was obtained.
549,10.1007/s10854-013-1527-1,solid_state_ceramic_synthesis,The BMN ceramic target was prepared by solid state ... r 6 h in air ambient after calcinated at 850 degC.
550,10.1002/fuce.201300250,solid_state_ceramic_synthesis,"Sr2-xSmxFe1.5Mo0.5O6 (0 <= x <= 0.4) samples were  ... te materials have been described elsewhere 17, 18."
551,10.1016/j.jeurceramsoc.2017.01.021,solid_state_ceramic_synthesis,"(1-x)K0.5Na0.5Nb0.997Cu0.0075O3-xSrZrO3 (x = 0, 0. ... , the pellets were embedded in self-source powder."
552,10.1016/j.matlet.2011.11.003,solid_state_ceramic_synthesis,The samples used in this study were prepared by co ... ntered at different temperatures in air for 0.5 h.
553,10.1016/j.jssc.2011.12.039,solid_state_ceramic_synthesis,"Gd2(Zr2-xCex)O7 samples (with 0<=x<=2, in interval ...  8 h in air on a stabilised zirconia setter plate."
554,10.1007/s10854-014-2637-0,solid_state_ceramic_synthesis,"CaSiO3 powders were prepared by a routine solid-st ...  of 1,275-1,375 degC for 2 h in an air atmosphere."
555,10.1016/j.matchemphys.2016.11.012,solid_state_ceramic_synthesis,(1-x)[0.8Bi0.5Na0.5TiO3-0.2Bi0.5K0.5TiO3]-xBiCoO3  ... overed alumina crucibles at the sintering process.
556,10.1111/j.1551-2916.2006.00942.x,solid_state_ceramic_synthesis,The ceramics were prepared using the conventional  ... s were sintered at temperatures at around 900degC.
557,10.1111/j.1551-2916.2007.02181.x,solid_state_ceramic_synthesis,"(Mg1-xZnx)Al2O4 (x=0, 0.2, 0.4, 0.6, 0.8, 1.0) cer ... properties were evaluated by the resonator method."
558,10.1007/s10854-013-1185-3,solid_state_ceramic_synthesis,The conventional solid-state reaction method was u ... position to restrain the volatilization of sodium.
559,10.1016/j.jeurceramsoc.2016.04.001,solid_state_ceramic_synthesis,"In this work, uniform and fine Mg0.27Al2.58O3.73N0 ... s ground to 2 mm in thickness and mirror-polished."
560,10.1007/s10854-014-2549-z,solid_state_ceramic_synthesis,"A series of Ni1-xZnxMn2O4 (0 <= x <= 1) NTC powder ... red pellets, and sintered at 835 degC for 20 mins."
561,10.1016/j.ssi.2014.06.009,solid_state_ceramic_synthesis,"Phase pure powders of SmxNd0.15 - xCe0.85O2 - δ (w ... lling for 24 h in ethanol, and drying at 120 degC."
562,10.1016/j.solidstatesciences.2006.01.017,solid_state_ceramic_synthesis,"Chemically pure BaCO3 (99%) and TiO2 (99%), and su ... ormally a suitable measure for sample compactness."
563,10.1016/j.matchemphys.2011.08.010,solid_state_ceramic_synthesis,"First, both ZnTiNb2O8 (ZTN) and BaCu(B2O5) (BCB) c ... pellets were sintered at 1200 degC for 2 h in air."
564,10.1016/j.jpowsour.2011.05.031,solid_state_ceramic_synthesis,"The compounds of nominal composition Li5La3Nb2-xYx ... eC2O4*2H2O, and MnCO3 at 700 degC for 24 h in air."
565,10.1007/s10854-016-6251-1,solid_state_ceramic_synthesis,Li3Mg2NbO6 + xwt.% ZBS (x = 0.1-3.0) ceramics were ...  degC for 4 h with the heating rate of 5 degC/min.
566,10.1016/j.jallcom.2007.06.128,solid_state_ceramic_synthesis,A conventional ceramic fabrication technique was u ... /mm at 180 degC in a silicone oil bath for 30 min.
567,10.1007/s10854-016-4450-4,solid_state_ceramic_synthesis,"The first, the copper vanadate sintering aids were ... e temperature range from 800 to 1050 degC for 4 h."
568,10.1016/j.ssi.2007.04.013,solid_state_ceramic_synthesis,"Powder samples of 20 at.% Sm-doped CeO2 (Ce0.8Sm0. ... the geometrical dimensions and weight, were 92.4%."
569,10.1016/j.jpowsour.2013.08.091,solid_state_ceramic_synthesis,"La1-xBaxCo1-yFeyO3-δ with 0.7 <= x <= 0.9 and 0.1  ... ample, in order to estimate the error of the data."
570,10.1016/j.jpowsour.2008.10.007,solid_state_ceramic_synthesis,A conventional solid-state reaction synthesis meth ...  density and electrical conductivity measurements.
571,10.1007/s10854-016-4388-6,solid_state_ceramic_synthesis,(1 - x)[0.98(0.95Na0.5K0.5NbO3-0.05LiSbO3)-0.02BiF ... icone oil which was 80 degC at 3 kV/mm for 20 min.
572,10.1016/j.matchemphys.2014.05.027,solid_state_ceramic_synthesis,NTN ceramics were prepared by conventional solid-s ...  and then sintered at 870-990 degC for 6 h in air.
573,10.1016/j.mseb.2011.03.006,solid_state_ceramic_synthesis,The (Pb0.97-xLa0.02Bax)(Zr0.75Sn0.12Ti0.13)O3 (PLB ...  the samples at 550 degC for 10 min as electrodes.
574,10.1016/j.ijhydene.2013.06.050,solid_state_ceramic_synthesis,Composite electrolyte with the composition of Ce0. ... ashed with mortar and pestle and denoted as LNCZO.
575,10.1016/j.jpowsour.2011.10.119,solid_state_ceramic_synthesis,The LSGM electrolyte material was prepared by soli ... e pellets were then sintered at 1450 degC for 6 h.
576,10.1111/j.1551-2916.2007.01960.x,solid_state_ceramic_synthesis,Ceramic samples with compositions corresponding to ... rformed in a tube furnace in an atmosphere of air.
577,10.1016/j.elecom.2013.08.018,solid_state_ceramic_synthesis,Copper delafossite samples were prepared using a c ... ds. Details of the synthesis are shown in Table 1.
578,10.1007/s10854-010-0176-x,solid_state_ceramic_synthesis,"(1 - x)BaTiO3-xBi0.5K0.5TiO3 (x = 0, 0.1 and 0.2)  ... nd 1,100 degC for different times of 0, 2 and 4 h."
579,10.1016/j.physb.2009.02.016,solid_state_ceramic_synthesis,Polycrystalline Ba0.80Pb0.20Ti1-xZrxO3 (x ranging  ... determined by using the Archimedes principle [13].
580,10.1007/s10854-014-2416-y,solid_state_ceramic_synthesis,"Na1/2Nd1/2Ti1-xSnxO3 samples with x = 0, 0.005, 0. ... ellets were sintered at 1,350 degC for 2 h in air."
581,10.1007/s10008-010-1235-1,solid_state_ceramic_synthesis,Sm1.92Ca0.08Ti2O7-δ was prepared via conventional  ... Zeiss SUPRA 35 scanning electron microscope (SEM).
582,10.1007/s10854-015-2856-z,solid_state_ceramic_synthesis,"Ca3-xBaxCo4O9 polycrystalline ceramic materials, w ... 0 degC for 24 h with a final furnace cooling [10]."
583,10.1016/j.jssc.2012.07.024,solid_state_ceramic_synthesis,HoMnO3 bulk powder was prepared by conventional so ... gC/h. The polycrystalline samples were >90% dense.
584,10.1016/j.matchemphys.2013.09.045,solid_state_ceramic_synthesis,Polycrystalline pure BFO and doped Bi1-xPrxFeO3 (x ... nes to form 2 mm thick and 15 mm diameter pellets.
585,10.1016/j.jeurceramsoc.2011.05.003,solid_state_ceramic_synthesis,BaCe0.8Y0.2-xNdxO3-δ (x = 0-0.2) powders were prep ...  the samples sintered at 1600 degC for 4 h in air.
586,10.1007/s10854-015-3547-5,solid_state_ceramic_synthesis,Sr5Nb4TiO17 powders were prepared by the mixed oxi ... nd annealing was carried out at 1200 degC for 4 h.
587,10.1007/s10854-013-1573-8,solid_state_ceramic_synthesis,Ga modified ceramic samples were prepared with the ...  degC for high temperature dielectric and testing.
588,10.1007/s10853-014-8498-3,solid_state_ceramic_synthesis,Bulk Al2Mo3O12 pellets were prepared in order to m ... .78 mm and a density fraction 73 % of theoretical.
589,10.1016/j.jpowsour.2011.12.011,solid_state_ceramic_synthesis,LiFePO4 was synthesized by solid-state reaction. T ... tmosphere. The carbon content of LiFePO4 is 2 wt%.
590,10.1007/s10854-008-9784-0,solid_state_ceramic_synthesis,The Ba2La2TiTa2O12 ceramics were prepared by conve ... g a controlled heating/cooling rate of 5 degC/min.
591,10.1007/s10853-009-3763-6,solid_state_ceramic_synthesis,The samples were prepared by the conventional soli ... using the heating and cooling rates of 5 degC/min.
592,10.1016/j.mseb.2014.09.001,solid_state_ceramic_synthesis,Pure and substituted LaAlO3 and La0.8Sr0.2Al1-xZnx ... ng stoichiometrically balanced equation (Eq. (5)):
593,10.1007/s10854-014-1899-x,solid_state_ceramic_synthesis,"The samples used in this study was prepared by the ... these samples were sintered at 1,310 degC for 4 h."
594,10.1016/j.mseb.2005.10.028,solid_state_ceramic_synthesis,Sr0.8Bi2.2(V0.2Nb0.8)2O9 ceramic sample was prepar ...  MPa. The disks were sintered for 6 h at 900 degC.
595,10.1007/s10854-017-6393-9,solid_state_ceramic_synthesis,The polycrystalline samples of Bi1-xNaxFe1-xNbxO3  ... se pellets were then sintered at 870 degC for 8 h.
596,10.1016/j.jeurceramsoc.2017.04.047,solid_state_ceramic_synthesis,The piezoelectric BNBK79 and BNBK79-Mn ceramics we ... wed by sintering in air at 1050-1150 degC for 2 h.
597,10.1007/s10853-014-8670-9,solid_state_ceramic_synthesis,The specimens with a composition of BaNd1.76Bi0.24 ...  for 4 h in air with a heating rate of 3 degC/min.
598,10.1016/j.matchemphys.2006.05.008,solid_state_ceramic_synthesis,"Stoichiometric ratios of La2O3, CaCO3, and Fe2O3 p ... mined by the Archimedes water immersion technique."
599,10.1007/s10854-012-1039-4,solid_state_ceramic_synthesis,Ca5-xLaxNb4-xTi1+xO17 samples with compositions va ... r 10 h to minimize the reduction of titanium ions.
600,10.1007/s10854-015-3999-7,solid_state_ceramic_synthesis,The produced materials SrBi2-xSmxNb2O9 (abbreviate ...  samples with about 0.3 mm in thickness were used.
601,10.1016/j.materresbull.2015.11.045,solid_state_ceramic_synthesis,Synthesis of PFT and PZT was performed by a conven ... to minimize the lead loss due to evaporation [13].
602,10.1016/j.ssc.2008.05.025,solid_state_ceramic_synthesis,The samples of BFTO were processed in two steps: f ... o pellets and sintered at 825 [?]C for 4 h in air.
603,10.1016/j.jeurceramsoc.2011.10.042,solid_state_ceramic_synthesis,MgWO4 and CaTiO3 compounds were individually synth ... BO3 were sintered at 900-1000 degC for 4 h in air.
604,10.1016/j.matlet.2009.02.063,solid_state_ceramic_synthesis,"In the present work, (1 - x)Pb(Zr1/2Ti1/2)O3-(x)Pb ...  2 h at a heating/cooling rate of 5 degC/min [14]."
605,10.1007/s10008-011-1484-7,solid_state_ceramic_synthesis,LiFePO4 was obtained by firing the mixture of acet ... milled for 30 min to obtain small-sized particles.
606,10.1007/s10854-015-3919-x,solid_state_ceramic_synthesis,The specimens were manufactured using a convention ... er a dc electric field of 3 kV/mm in silicone oil.
607,10.1016/j.jeurceramsoc.2005.03.075,solid_state_ceramic_synthesis,Ceramic disk samples of 0.12PNS-0.48PT-0.40PZ + α  ... hat of the Institute of Radio Engineers Standard.4
608,10.1016/j.ssc.2008.02.004,solid_state_ceramic_synthesis,Polycrystalline Bi4Ti2Fe0.5Nb0.5O12 powders were s ... ature density ~ 0.86 gm/cm3) as the liquid medium.
609,10.1007/s10008-008-0637-9,solid_state_ceramic_synthesis,"Solid solutions of Bi2O3-based systems were synthe ... l etching between 900 degC and 1,100 degC for 3 h."
610,10.1016/j.solmat.2008.05.001,solid_state_ceramic_synthesis,The LSMO samples were prepared by conventional sol ... ring temperature of 1473 K for a duration of 24 h.
611,10.1007/s10854-012-0627-7,solid_state_ceramic_synthesis,Single phase CCTO powder was prepared by the solid ... 00degC for 10 h to form composite ceramic samples.
612,10.1016/j.jeurceramsoc.2015.12.033,solid_state_ceramic_synthesis,"MgTi1-x(Mg1/3B2/3)xO3 (B = Nb, Ta) (0.03 <= x <= 0 ... pellets were sintered at 1400 degC for 4 h in air."
613,10.1016/j.jpowsour.2009.12.081,solid_state_ceramic_synthesis,The samples SCNy (y = 0.00-0.20) were synthesized  ...  were obtained by sintering at 1450 degC for 10 h.
614,10.1016/j.jpowsour.2009.02.072,solid_state_ceramic_synthesis,The intergrowth perovskite oxide powders were prep ... termediate grinding in an agate mortar after 12 h.
615,10.1016/j.jpowsour.2008.08.039,solid_state_ceramic_synthesis,"La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM8282), La0.8Sr0.2Ga0 ... fied using X-ray diffraction (Panalytical X'pert)."
616,10.1111/j.1551-2916.2007.01983.x,solid_state_ceramic_synthesis,Pure and Al-doped CCTO ceramics were prepared by t ... ensification (96%-97% of the theoretical density).
617,10.1007/s10854-012-0774-x,solid_state_ceramic_synthesis,"In this experiment, x mol% Y-doped 99 mol%BaTiO3-1 ... egC for 10 min in air for electrical measurements."
618,10.1016/j.matlet.2010.07.048,solid_state_ceramic_synthesis,A conventional solid state reaction route was appl ... red alumina crucibles at 1175 degC for 2 h in air.
619,10.1016/j.jpcs.2011.12.005,solid_state_ceramic_synthesis,"In this experiment, we fabricated 5 wt% CuO-doped  ... repared. The reaction can be expressed as follows:"
620,10.1111/j.1551-2916.2008.02614.x,solid_state_ceramic_synthesis,Sample of (Mg1-xZnx)2TiO4 was synthesized by a con ... t temperatures of 1270deg-1390degC for 4 h in air.
621,10.1016/j.optmat.2009.08.006,solid_state_ceramic_synthesis,A series of Mg1-xMnxY1-yCeySi2O5N powders were syn ... eated and cooled at a constant rate of 300 degC/h.
622,10.1016/j.matlet.2010.11.021,solid_state_ceramic_synthesis,"SnO2 ceramics containing Mn of 5, 10, 15, and 20 m ... air, with heating and cooling rates of 5 degC/min."
623,10.1016/j.ssi.2011.10.013,solid_state_ceramic_synthesis,The BSCF powder was synthesized by the solid state ... y ball-milling to a particle size of about 3.1 μm.
624,10.1016/j.matlet.2012.02.066,solid_state_ceramic_synthesis,"Samples of (Mg0.95M0.05)Ta2O6 (M = Ni, Zn, Mn) wer ... ts were sintered at 1450-1575 degC for 2 h in air."
625,10.1007/s10854-006-9007-5,solid_state_ceramic_synthesis,Ba5-3x/2La1+xTi3Ta7O30 (x = 0 to 3.0) ceramics wer ... 0degC in air for 3 h to obtain the dense ceramics.
626,10.1016/j.jssc.2014.01.019,solid_state_ceramic_synthesis,"Synthesis of the sample Bi25FeO39 is carried out b ... section, and annealed at of 1073 K in air for 4 h."
627,10.1016/j.ssi.2016.01.044,solid_state_ceramic_synthesis,"A series of Li1 + xAlxZr2-x(PO4)3 (x = 0, 0.2, 0.4 ... himedes method using water as the immersion fluid."
628,10.1016/j.apsusc.2008.02.113,solid_state_ceramic_synthesis,Type A powders were obtained by a simple mechanica ...  flowability of feedstock powders during spraying.
629,10.1016/j.scriptamat.2011.11.014,solid_state_ceramic_synthesis,YMnO3 powders were prepared by solid-state reactio ... sed at 200 MPa and then sintered 5 h at 1400 degC.
630,10.1016/j.jeurceramsoc.2010.11.015,solid_state_ceramic_synthesis,Ceramic samples in the BF-PZ-PT ternary system wer ... to minimize the evaporation loss of PbO and Bi2O3.
631,10.1016/j.jpcs.2016.03.014,solid_state_ceramic_synthesis,Ceramic samples of BTO and Ba0.98Zn0.02Ti1-xMnxO3  ... 1300 degC for 5 h at a heating rate of 3 degC/min.
632,10.1007/s10854-015-3996-x,solid_state_ceramic_synthesis,The composition \(\hbox {Ba}_{0.85}\hbox {Sr}_{0.1 ... gain at 300 degC for 6 h to evaporate the alcohol.
633,10.1016/j.matlet.2016.05.010,solid_state_ceramic_synthesis,The BCZT-BMN ceramics were prepared by conventiona ... es in order to characterize electrical properties.
634,10.1016/j.ssi.2012.03.045,solid_state_ceramic_synthesis,Li1.3Al0.3Ti1.7(PO4)3 has also been prepared by so ... cs have been sintered at 1000 degC for 2 h in air.
635,10.1016/j.matlet.2013.05.017,solid_state_ceramic_synthesis,"Ca1-xNaxCu3Ti4O12 (x=0, 0.02, and 0.10) powders we ...  CCTO, CNCTO-1, and CNCTO-2 samples, respectively."
636,10.1016/j.electacta.2010.12.041,solid_state_ceramic_synthesis,C-LFP raw material was prepared via a solid state  ... ed at 700 degC for 10 h under nitrogen atmosphere.
637,10.1016/j.mseb.2007.07.092,solid_state_ceramic_synthesis,Perovskite manganese oxides with nominal compositi ...  were rapidly quenched to room temperature in air.
638,10.1007/s10854-013-1284-1,solid_state_ceramic_synthesis,"The samples used in this study were prepared by th ... these samples were sintered at 1,350 degC for 6 h."
639,10.1016/j.ssi.2014.08.004,solid_state_ceramic_synthesis,The ESB target material was prepared using powder  ... arting powders was confirmed by X-ray diffraction.
640,10.1016/j.jeurceramsoc.2014.05.046,solid_state_ceramic_synthesis,"The La2-xLuxZr2O7 (x = 0, 0.2, 0.4, 0.6, 0.8, 1.0, ... hed on both sides to a thickness of 1 mm for test."
641,10.1007/s10854-014-2031-y,solid_state_ceramic_synthesis,"The ferroelectric ceramics, which had a compositio ... th with a field strength of 7-12 kV/mm for 10 min."
642,10.1016/j.mseb.2013.05.007,solid_state_ceramic_synthesis,Sr0.6-x(LiCe)x/2.5(BiNa)0.2Bi2Nb2O9 (SLCBNBNO) cer ... d by alumina crucible followed by furnace cooling.
643,10.1016/j.jpowsour.2007.02.022,solid_state_ceramic_synthesis,La0.8Sr0.2Ga0.8Mg0.2O3 (LSGM) used as the electrol ... ty) and then sintered at 1500 degC for 6 h in air.
644,10.1007/s10853-016-9813-y,solid_state_ceramic_synthesis,"The ceramics (Ca0.4,Sr0.6)Bi4Ti4O15 with x mol% Mn ... r 30 min under a DC electric field of 10-14 kV/mm."
645,10.1016/j.jeurceramsoc.2012.06.002,solid_state_ceramic_synthesis,La3Ti2TaO11 powders were prepared by high temperat ... e powders were calcined at 1300-1450 degC for 4 h.
646,10.1016/j.mseb.2009.05.019,solid_state_ceramic_synthesis,Sodium bismuth titanate piezoelectric ceramics wer ... amics were also produced under the same procedure.
647,10.1016/j.electacta.2011.07.130,solid_state_ceramic_synthesis,"Neodymium oxide, ceric oxide and cupric oxide with ... ferred to as NCCO(SSR) and NCCO(MR), respectively."
648,10.1007/s10854-017-6442-4,solid_state_ceramic_synthesis,"Na0.25K0.25Bi2.5Nb2O9-Pr3+ (NKBN-xPr) (x = 0.00, 0 ... 10 min for the electrical performance measurement."
649,10.1016/j.jeurceramsoc.2005.03.135,solid_state_ceramic_synthesis,"Ceramic samples of composition Ba3(Mg1-xZn1-x)Nb2O ...  1 h in air, using a 200 K/h heating/cooling rate."
650,10.1016/j.jeurceramsoc.2012.03.030,solid_state_ceramic_synthesis,Sample of Li2TiO3 was synthesized by conventional  ... and the cooling rate were both set at 10 degC/min.
651,10.1016/j.matlet.2014.09.082,solid_state_ceramic_synthesis,Li-Ni co-doped polycrystalline SnO2 with nominal c ...  annealing by shutting off the electricity source.
652,10.1016/j.jpcs.2011.12.013,solid_state_ceramic_synthesis,The composition of the different specimens can be  ... n method have been reported earlier [13] and [14].
653,10.1016/j.jeurceramsoc.2016.05.033,solid_state_ceramic_synthesis,"The (Ba0.85Ca0.15)(Zr0.1Ti0.9)O3 (BCZT) was synthe ... technique (Micromeritics, Accu Pyc 1330, GA, USA)."
654,10.1016/j.electacta.2015.07.170,solid_state_ceramic_synthesis,The starting materials used for LATP synthesis by  ... d dried at 80 degC for 12 h to obtain LATP powder.
655,10.1007/s10854-012-0752-3,solid_state_ceramic_synthesis,The (1 - y)La0.97Sm0.03(Mg0.5Sn0.5)O3-yCa0.8Sm0.4/ ... rate and the cooling rate were set at 10 degC/min.
656,10.1016/j.mseb.2006.07.023,solid_state_ceramic_synthesis,"(1 - x)(Na0.5La0.5)TiO3 + xCeO2 + 1 wt.% CuO (x =  ...  + 1 wt.% CuO and CeO2 + 1 wt.% CuO, respectively."
657,10.1016/j.ssc.2006.06.019,solid_state_ceramic_synthesis,"Potassium lanthanum bismuth tantalate, K0.5La0.5Bi ... ve density of the pellet was determined to be 95%."
658,10.1007/s10854-015-4058-0,solid_state_ceramic_synthesis,Li4xMg3(1-x)Al6(1-x)Ti5xO12 ceramics were prepared ... in and then cooled in furnace to room temperature.
659,10.1016/j.ssi.2010.07.034,solid_state_ceramic_synthesis,BaCe0.9Nd0.1O3 - δ powders were prepared by a conv ...  of homogeneous shape and uniformed particle size.
660,10.1016/j.jallcom.2014.11.178,solid_state_ceramic_synthesis,The phosphors were prepared via solid-state reacti ... us powders (marked as Tb3+:LiMgPO4) were obtained.
661,10.1016/j.jallcom.2004.06.046,solid_state_ceramic_synthesis,"Powder mixtures based on the formula LixLa1-xMnO3  ... 0 degC for 24 h, followed by grinding and sieving."
662,10.1016/j.jpowsour.2003.11.084,solid_state_ceramic_synthesis,All starting powders with sub-micron order were pr ... by sintering at 1500 or 1400 degC for 10 h in air.
663,10.1016/j.jmmm.2006.07.025,solid_state_ceramic_synthesis,"In general, the conventional solid-state reaction  ... ly been used to synthesize such ceramic materials."
664,10.1016/j.ssc.2009.02.028,solid_state_ceramic_synthesis,La2NiMnO6 ceramics were prepared via a solid state ... llets were 1.5 mm in height and 10 mm in diameter.
665,10.1016/j.jpcs.2014.01.023,solid_state_ceramic_synthesis,Ba0.85Ca0.15Ti1-x(Mg1/2W1/2)xO3 ceramics were prep ... der and then sintered at 1450 degC for 4 h in air.
666,10.1007/s10854-015-3757-x,solid_state_ceramic_synthesis,"(1 - x)BNTBT-xNBN (x = 0, 0.05, 0.10, 0.20, 0.30,  ... he pellets were embedded with self-source powders."
667,10.1016/j.jallcom.2010.08.026,solid_state_ceramic_synthesis,Ceramics of 0.05Pb(Mg1/3Ta2/3)O3-0.05Pb(Mn1/3Sb2/3 ... es of the samples were measured 24 h after poling.
668,10.1007/s10854-013-1161-y,solid_state_ceramic_synthesis,Specimens of the ZnO-V2O5-based ceramics were prep ... s electrodes after heating at 600 degC for 30 min.
669,10.1016/j.jeurceramsoc.2005.03.078,solid_state_ceramic_synthesis,"Reagent grade oxide powders of PbO, BaCO3, MgO, Nb ... s were ground by ball milling in ethanol for 60 h."
670,10.1016/j.tsf.2006.01.047,solid_state_ceramic_synthesis,A Pb(Zr00.65Ti0.35)O3 target with 10 wt.% excess P ... y of the target was measured by Archimedes method.
671,10.1016/j.jpcs.2007.08.066,solid_state_ceramic_synthesis,"(1-x)NKN-xBF ceramics (x=0, 0.005, 0.01, 0.02, 0.0 ... d as above for 24 h and sieved through 230 meshes."
672,10.1016/j.jeurceramsoc.2017.04.065,solid_state_ceramic_synthesis,TiO2 doped YbSZ powders were produced by a solid s ... o-physical and mechanical properties measurements.
673,10.1007/s10853-011-6129-9,solid_state_ceramic_synthesis,"The samples of BFTO-1 and BFCT-1 were obtained by  ... lets, then sintered at 1020 and 1040 degC for 4 h."
674,10.1016/j.jpowsour.2012.07.122,solid_state_ceramic_synthesis,Mixed oxygen ion-electron conducting LSCF1982 powd ... with stabilized zirconia balls for 4 h at 320 rpm.
675,10.1016/j.scriptamat.2008.06.016,solid_state_ceramic_synthesis,The fabrication of PZT/ZnOw nanocomposites was per ...  for 20 min with an electric field of 3-4 kV mm-1.
676,10.1016/j.materresbull.2015.06.024,solid_state_ceramic_synthesis,All samples were synthesized by a high temperature ... ound and then calcined at 750 degC in air for 4 h.
677,10.1016/j.mseb.2012.02.016,solid_state_ceramic_synthesis,The ingredient raw powders of the (1-x)BFO-xBCN (x ... mpositions were performed with at least 5 samples.
678,10.1016/j.jeurceramsoc.2013.04.004,solid_state_ceramic_synthesis,"A conventional solid-state reaction method was use ... for 3 h in air, with a heating rate of 3 degC/min."
679,10.1007/s10854-016-4949-8,solid_state_ceramic_synthesis,"The polycrystalline sample of Bi3La2Ti3FeO15 was p ... or 4 h, before taking any electrical measurements."
680,10.1016/j.mseb.2015.08.006,solid_state_ceramic_synthesis,The Aurivillius-type CBT ceramic samples with coba ... them were polished to a thickness of about 0.8 mm.
681,10.1016/j.jeurceramsoc.2006.02.004,solid_state_ceramic_synthesis,Specimens were prepared by a conventional mixed ox ... ensities were determined by the Archimedes method.
682,10.1016/j.tsf.2005.07.202,solid_state_ceramic_synthesis,The target composition of (Zr0.8Sn0.2)TiO4 was syn ... rs and 6-mm thicknesses to be used as ZST targets.
683,10.1016/j.physb.2006.04.027,solid_state_ceramic_synthesis,"The (Pb1-xBax)ZrO3, 0x0.30, ceramics were prepared ... ssed at 80 MPa into a pellet of 15 mm in diameter."
684,10.1016/j.ceramint.2003.12.030,solid_state_ceramic_synthesis,Specimen powders were prepared by conventional sol ... llets and then sintered at about 960 degC for 2 h.
685,10.1007/s10854-013-1082-9,solid_state_ceramic_synthesis,"Nd123 samples, prepared by solid state reaction me ... cesses were performed the same for each content x."
686,10.1016/j.jallcom.2010.05.114,solid_state_ceramic_synthesis,Samples of the MgO ceramics were synthesized by th ... and the cooling rate were both set at 10 degC/min.
687,10.1007/s10854-014-2373-5,solid_state_ceramic_synthesis,Specimen powders are prepared by conventional soli ... t the Ti4+ reduction during the sintering process.
688,10.1016/j.matlet.2010.04.031,solid_state_ceramic_synthesis,A conventional solid state reaction route was appl ... ered alumina crucible at 1080 degC for 1 h in air.
689,10.1016/j.jeurceramsoc.2014.07.026,solid_state_ceramic_synthesis,"The (K0.50Na0.50)1-xLix(Nb0.80Ta0.20)O3 ceramics ( ... gC, 1135 degC and 1125 degC for 2 h, respectively."
690,10.1016/j.matchemphys.2011.05.037,solid_state_ceramic_synthesis,The ceramics were prepared using conventional mixe ... were subsequently sintered at 840-920 degC in air.
691,10.1016/j.corsci.2010.02.040,solid_state_ceramic_synthesis,Powders of pure metal oxides were used to prepare  ... sted and the powders used in the current research.
692,10.1007/s10854-014-2613-8,solid_state_ceramic_synthesis,"High purity powders of commercial Bi2O3 (Panreac,9 ...  850 degC for 120 h in air to produce the Bi-2212."
693,10.1007/s10853-012-6326-1,solid_state_ceramic_synthesis,Ba0.85Ca0.15Ti0.90Zr0.10O3 + x mol% CuO (BCZT - x) ... /mm at ~30 degC in a silicone oil bath for 30 min.
694,10.1016/j.jpowsour.2011.02.010,solid_state_ceramic_synthesis,"The samples, formulated as [(ZrO2)1-x(CeO2)x]0.92( ...  mixing method, and sintered at 1600 degC for 4 h."
695,10.1016/j.ssi.2015.06.009,solid_state_ceramic_synthesis,The LLZ precursor was prepared by solid state reac ... t was used for characterization and further study.
696,10.1016/j.mseb.2005.11.015,solid_state_ceramic_synthesis,LiMn0.6Fe0.4PO4/nano-carbon webs composite was pre ... site was prepared by the same procedures as above.
697,10.1016/j.ijhydene.2016.01.071,solid_state_ceramic_synthesis,The BaFe0.85Cu0.15O3-δ (BFC) powders were prepared ... was about 1 mm in thickness and 15 mm in diameter.
698,10.1016/j.jallcom.2011.03.006,solid_state_ceramic_synthesis,Na-β''-Al2O3 solid electrolytes doped with TiO2 ar ... time at 1450 degC in the cooling process is added.
699,10.1016/j.mseb.2004.06.011,solid_state_ceramic_synthesis,A Pb(Zr0.65Ti0.35)O3 target with 40 wt.% excess Pb ... osition of thin films by PLD are given in Table 1.
700,10.1016/j.jallcom.2015.07.152,solid_state_ceramic_synthesis,To prepare BiFeO3 by conventional solid-state reac ... ed pellets were used for further characterization.
701,10.1111/j.1551-2916.2005.00800.x,solid_state_ceramic_synthesis,Ba(Cd1/3Ta2/3)O3 ceramics were synthesized by a co ... ere subsequently annealed at 1250degC for 20~80 h.
702,10.1016/j.matlet.2014.11.114,solid_state_ceramic_synthesis,BCZN ceramics were prepared with high-purity (>99. ... s were sintered at 1350-1450 degC for 12 h in air.
703,10.1016/j.jeurceramsoc.2005.03.076,solid_state_ceramic_synthesis,PIN-xPT perovskite powders were synthesised by sol ... ceramics with high densities (>98%) were achieved.
704,10.1016/j.matlet.2016.04.021,solid_state_ceramic_synthesis,To synthesize the La-BNT ceramics we have chosen s ... re brought to room temperature by natural cooling.
705,10.1016/j.jeurceramsoc.2005.09.003,solid_state_ceramic_synthesis,BiNbO4 ceramics were prepared by the conventional  ...  an alumina crucible to inhibit the loss of Bi2O3.
706,10.1016/j.jeurceramsoc.2016.03.010,solid_state_ceramic_synthesis,The La2Zr2O7/LaPO4 composites with varied LaPO4 co ... isks of 1 mm x Φ10 mm for thermal roperties tests.
707,10.1007/s10854-016-4737-5,solid_state_ceramic_synthesis,The (LaMn0.5Co0.5O3)x-(Ni0.66Mn2.34O4)1-x samples  ... ively. Then the expectant pure phase was obtained.
708,10.1016/j.mseb.2007.01.020,solid_state_ceramic_synthesis,The Zn0.96Mn0.04O powder was prepared using solid- ... ground for 3 h to get a homogeneous powder sample.
709,10.1016/j.matlet.2015.09.063,solid_state_ceramic_synthesis,(Nd1-xLax)1.02Nb0.988O4 microwave dielectric ceram ... intered at temperatures of 1225-1275 degC for 4 h.
710,10.1016/j.matlet.2004.02.050,solid_state_ceramic_synthesis,The ferrite samples with the representative formul ... measurements were carried out at room temperature.
711,10.1016/j.jpowsour.2009.11.062,solid_state_ceramic_synthesis,BICUVOX10 powder was prepared by means of a solid- ...  sieve was used to remove any oversized particles.
712,10.1007/s10854-016-6039-3,solid_state_ceramic_synthesis,"(1 - x)(K0.5Na0.5)NbO3-xBi(Mg0.75W0.25)O3 [(1 - x) ... MW, ranging from 1100 to 1210 degC for 2 h in air."
713,10.1007/s10854-013-1136-z,solid_state_ceramic_synthesis,"The ceramics based on Ba0.5Sr0.5TiO3-MgMoO4 specim ... r, and then sintered at 1,350 degC for 4 h in air."
714,10.1007/s10854-015-3562-6,solid_state_ceramic_synthesis,Sample of BaO + 0.6ZnO + 2.9TiO2 was separately sy ... e samples were sintered at 825-950 degC for 1.5 h.
715,10.1016/j.ssi.2014.05.016,solid_state_ceramic_synthesis,Li1.5Al0.5Ge1.5(PO4)3 was synthesized by solid-sta ... in a box furnace again at 800 degC for 2 h in air.
716,10.1007/s10854-016-5765-x,solid_state_ceramic_synthesis,The ZST and BV ceramics were both synthesized thro ... n the temperature range of 1250-1350 degC for 5 h.
717,10.1016/j.mseb.2013.01.003,solid_state_ceramic_synthesis,Mg(Zr0.05Ti0.95)O3 and SrTiO3 powders were synthes ...  air with heating and cooling rate of 10 degC/min.
718,10.1007/s10854-017-6494-5,solid_state_ceramic_synthesis,"BaTiO3 powders were prepared by the conventional s ... nvironment, with oxygen rate is 6 ml/min) for 2 h."
719,10.1016/j.materresbull.2012.05.061,solid_state_ceramic_synthesis,"Yb0.1Ca0.9-xDyxMnO3, with x = 0.02, 0.05, 0.08 and ... x 1.8 mm to measure the thermoelectric properties."
720,10.1002/ente.201600456,solid_state_ceramic_synthesis,"The BaTiO3 ceramic samples were fabricated by conv ... cm-3, that is, beyond 97 % of theoretical density."
721,10.1007/s10854-015-4072-2,solid_state_ceramic_synthesis,Specimens were prepared through conventional solid ... pure SBN sample was sintered at 1325 degC for 3 h.
722,10.1007/s10854-015-3246-2,solid_state_ceramic_synthesis,Samples of (1 - x) BiVO4-xLi0.5Re0.5WO4 (x = 0.05- ... ed at temperatures of 650-800 degC for 4 h in air.
723,10.1016/j.powtec.2013.11.006,solid_state_ceramic_synthesis,"LiMn2 - xAlxO4 (x = 0, 0.05, 0.1, 0.15) were prepa ... and then calcined at 750-800 degC for 10 h in air."
724,10.1016/j.jeurceramsoc.2009.02.015,solid_state_ceramic_synthesis,BIT was prepared using a conventional solid-state  ...  out at 900 degC for 2 h in a nitrogen atmosphere.
725,10.1016/j.jpowsour.2011.03.016,solid_state_ceramic_synthesis,Sr1.5LaxMnO4 powders were prepared by conventional ... te reaction and uniform composition were achieved.
726,10.1016/j.jallcom.2014.11.107,solid_state_ceramic_synthesis,(NaBi)0.48-x(LiCe)x[ ]0.04Bi2Nb1.97W0.03O9 (LCNBNW ...  ~20 min under a DC electric field of 10-11 kV/mm.
727,10.1016/j.jmmm.2015.01.069,solid_state_ceramic_synthesis,W-type strontium hexaferrite with composition of S ... degC for 2 h with the heating rate of 10 degC/min.
728,10.1007/s10854-016-5768-7,solid_state_ceramic_synthesis,"Y-type hexagonal ferrites (Ba2Co2-xCuxFe12O22, x = ... en the samples were sintered at l100 degC for 4 h."
729,10.1002/app.32480,solid_state_ceramic_synthesis,LiNi1/3Co1/3Mn1/3O2 cathode material was synthesiz ... h and finally calcined at 950degC for 16 h in air.
730,10.1007/s10854-015-3569-z,solid_state_ceramic_synthesis,Bi0.9Ba0.1Fe1-xCrxO3 ceramic materials substituted ... mpacted samples were sintered at 825 degC for 1 h.
731,10.1007/s10854-011-0319-8,solid_state_ceramic_synthesis,"The fabrication of PZT/xZnOw (x = 0, 1, 2, 5, 8, 1 ... degC for 20 min with an electric field of 3 kV/mm."
732,10.1002/pssr.200802225,solid_state_ceramic_synthesis,"The pure and cobalt-modified Na0.5Bi4.5Ti4O15 comp ... NBT-C2, NBT-C3, NBT-C4, and NBT-C5, respectively)."
733,10.1016/j.ssi.2009.12.016,solid_state_ceramic_synthesis,BaxCo0.7Fe0.2Nb0.1O3 - δ (BxCFN) compounds with x  ... conductivity and oxygen permeability measurements.
734,10.1016/j.jeurceramsoc.2016.08.021,solid_state_ceramic_synthesis,The (0.67-x)BF-0.33BT-xLMT (x = 0-0.08) ceramics w ... ilver paste and then fired at 550 degC for 30 min.
735,10.1111/j.1551-2916.2006.01461.x,solid_state_ceramic_synthesis,The CLNT powder compositions were synthesized by t ... -960degC for 2 h at a heating rate of 2.5degC/min.
736,10.1016/j.materresbull.2011.03.034,solid_state_ceramic_synthesis,"In this paper, the 0.35BiScO3-0.60PbTiO3-0.05Pb(Zn ...  the same composition was put inside the crucible."
737,10.1016/j.jpowsour.2016.11.005,solid_state_ceramic_synthesis,"BaZr0.85Y0.15O3-d (BZY) powders were synthesized b ... sing a density meter (MD300S, Alfa Mirage, Japan)."
738,10.1007/s10853-012-6280-y,solid_state_ceramic_synthesis,The polycrystalline ceramic disks from modified PZ ...  1070 degC for 4 h using sealed alumina crucibles.
739,10.1016/j.matchemphys.2013.10.002,solid_state_ceramic_synthesis,Eight mole percent of yttria-stabilised zirconia c ... at 1100 degC for 10 min to produce the electrodes.
740,10.1016/j.physe.2011.11.019,solid_state_ceramic_synthesis,"BiVO4 powder was prepared by means of a convention ... gate pots and balls, at a speed of 600 rpm in air."
741,10.1016/j.jpowsour.2014.05.147,solid_state_ceramic_synthesis,"The Li2Fe1-xNixP2O7/C (x = 0.02, 0.04, 0.06, 0.08, ... for 10 h at 650 degC in argon (99.999% in purity)."
742,10.1007/s10854-016-4752-6,solid_state_ceramic_synthesis,Ceramics based on system 0.7(SryCa1-y)TiO3-0.3(Smx ... re then sintered at 1440-1560 degC for 4 h in air.
743,10.1016/j.mseb.2004.04.019,solid_state_ceramic_synthesis,The conventional solid state reaction method was u ... silicon oil at 80 degC under 3-4 kV/mm for 15 min.
744,10.1016/j.actamat.2007.08.011,solid_state_ceramic_synthesis,All ferrite samples were synthesized via the conve ... samples were used for measurement of permeability.
745,10.1016/j.matchemphys.2010.01.014,solid_state_ceramic_synthesis,Polycrystalline samples of Sr5PrTi3Nb7O30 and Sr4P ...  air at 1350 degC for 8 h to yield dense ceramics.
746,10.1111/j.1551-2916.2007.01825.x,solid_state_ceramic_synthesis,"BaZr0.35Ti0.65O3 powder was prepared by the conven ... ponded to Samples A, B, C, D, and E, respectively."
747,10.1111/j.1551-2916.2009.03077.x,solid_state_ceramic_synthesis,Samples of Zn(Nb1-xTax)2O6 were synthesized by a c ...  were sintered at 1100deg-1225degC for 2 h in air.
748,10.1007/s10854-016-4964-9,solid_state_ceramic_synthesis,BaZr0.2Ti0.8O3 ceramics were fabricated by solid-s ... samples as electrodes for electrical measurements.
749,10.1016/j.ceramint.2015.07.023,solid_state_ceramic_synthesis,Polycrystalline ceramics of BaTi1-xMnxO3 where x=0 ... C/min and thereafter it was cooled at 10 degC/min.
750,10.1007/s10854-012-0924-1,solid_state_ceramic_synthesis,"BaHf0.1Ti0.9-xZrxO3 (x = 0, 0.02, 0.04, 0.10) cera ... afnate were sintered at 1,350 degC for 4 h in air."
751,10.1016/j.materresbull.2015.02.035,solid_state_ceramic_synthesis,(1 - x) BiFeO3-x (Ba0.85Ca0.15)(Zr0.10Ti0.90)O3 [( ... intered ceramics and fired at 840 degC for 30 min.
752,10.1016/j.jpowsour.2010.08.057,solid_state_ceramic_synthesis,BSM (Bi0.5Sr0.5MnO3) powder was synthesized using  ... ical density as measured by the Archimedes method.
753,10.1016/j.jssc.2008.07.009,solid_state_ceramic_synthesis,"Sr4AlNbO8 was synthesized by a solid-state reactio ... 6-2xNb2+2xO11+3x (x[?]0.23) [5], and Sr2AlNbO6[1]."
754,10.1016/j.scriptamat.2010.10.006,solid_state_ceramic_synthesis,Ca2TiMnO6 (CTM) ceramic was fabricated by the conv ... oding with a post-fire silver paste on both sides.
755,10.1016/j.electacta.2011.02.016,solid_state_ceramic_synthesis,The LSCO powders were synthesized by the conventio ... 19 g/m2 measured by BET surface adsorption method.
756,10.1016/j.jpowsour.2016.05.089,solid_state_ceramic_synthesis,"The target material was synthesized via a conventi ... δ, BFI) were also prepared, using the same method."
757,10.1016/j.jeurceramsoc.2008.04.033,solid_state_ceramic_synthesis,The KLNNSx-y (x = 0-4 mol% and y = 0-8 mol%) ceram ... silicone oil at 120 degC under 4 kV/mm for 30 min.
758,10.1016/j.jpcs.2006.08.004,solid_state_ceramic_synthesis,"Undoped and yttrium-doped SrTiO3 powders (YxSr1-xT ... ructure, and electrical conductivity measurements."
759,10.1111/j.1551-2916.2011.04495.x,solid_state_ceramic_synthesis,The Pb0.92Ba0.08Nb2O6-0.25 wt% TiO2 (PBNT) ceramic ... d with the corresponding powders during sintering.
760,10.1016/j.mseb.2003.09.034,solid_state_ceramic_synthesis,Pb(Zr0.52Ti0.48)O3 and Pb(Zr0.97Ti0.03)O3 powders  ... e of -1 degC/min to avoid cracking during cooling.
761,10.1016/j.ssi.2010.09.030,solid_state_ceramic_synthesis,MDLS powder with the chemical composition of La9.7 ... ders are used for fabrication of anode substrates.
762,10.1016/j.matlet.2013.03.019,solid_state_ceramic_synthesis,"Ca1-xSnSiO5:Dyx3+ (x=0.01, 0.015, 0.02, 0.025) and ...  furnace and sintered at 1380 degC for 4 h in air."
763,10.1007/s10854-015-3284-9,solid_state_ceramic_synthesis,Conventional solid state reaction procedure was us ... pellets are above 97 % of the theoretical density.
764,10.1002/pssa.200925192,solid_state_ceramic_synthesis,The BLSTPTx (x = 0.60-0.65) ceramics were prepared ... sintered in sealed crucibles at 1100 degC for 2 h.
765,10.1016/j.jallcom.2010.11.128,solid_state_ceramic_synthesis,SmBaCoCuO5+x (SBCCO) oxides were synthesized by co ... ined at 800 degC for 2 h to obtain the GDC powder.
766,10.1016/j.jssc.2012.08.054,solid_state_ceramic_synthesis,"Zn,W co-substituted BaTiO3 perovskite ceramics wit ... temperature from 1300 to 1425 degC for 4 h in air."
767,10.1016/j.jeurceramsoc.2010.05.027,solid_state_ceramic_synthesis,Ceramic powders with compositions (K0.44+xNa0.52Li ... 00 degC for 2 h with a heating rate of 3 degC/min.
768,10.1007/s10854-011-0611-7,solid_state_ceramic_synthesis,"Lead-free (K0.4425Na0.52Li0.0375)(Nb0.87Ta0.06Sb0. ... ntly, sintered in air at 1,040-1,120 degC for 3 h."
769,10.1016/j.snb.2013.08.020,solid_state_ceramic_synthesis,Samples of BiFeO3 ceramic have been obtained by a  ... .81 x 1011 N m-2 (parameters at room temperature).
770,10.1016/j.jeurceramsoc.2003.09.026,solid_state_ceramic_synthesis,BIT was also prepared by solid-state reaction to b ... again for 108 h and calcined at 750 degC for 10 h.
771,10.1016/j.jeurceramsoc.2016.04.024,solid_state_ceramic_synthesis,BNT-based lead-free piezoceramics with nominal com ... egC for 1 h to finalize the densification process.
772,10.1016/j.matlet.2013.12.002,solid_state_ceramic_synthesis,The samples were prepared in the following steps.  ... ted disc was sintered at 1220 degC for 3 h in air.
773,10.1016/j.matlet.2009.01.024,solid_state_ceramic_synthesis,The phosphor was synthesized by a general high tem ... ucts were crystalline Sr4Si3O8Cl4: Eu2+ phosphors.
774,10.1016/j.jallcom.2005.08.097,solid_state_ceramic_synthesis,Eu0.5Zr2(PO4)3 was prepared by a conventional soli ... ned at 1200 degC for 5 h in a flow of 2%H2-Ar gas.
775,10.1016/j.cplett.2005.05.059,solid_state_ceramic_synthesis,The transparent ceramic samples of Tm3+-doped PLZT ...  Kα radiation (1.5406 Å) in the 2θ range 10-80deg.
776,10.1016/j.jeurceramsoc.2015.04.038,solid_state_ceramic_synthesis,Y3(1+x)Al5O12 ceramics with x changed from -4.3% t ... acted by cold isostatic pressing (CIP) at 250 MPa.
777,10.1007/s10854-016-4547-9,solid_state_ceramic_synthesis,Samples of (Zr0.8Sn0.2)TiO4 were synthesized by co ... emperatures from 1300 to 1360 degC for 5 h in air.
778,10.1016/j.matlet.2015.05.111,solid_state_ceramic_synthesis,"Ceramics were prepared by a conventional mixed oxi ... LMW powders, and then sintered at 85 degC for 2 h."
779,10.1007/s10853-015-9446-6,solid_state_ceramic_synthesis,A conventional solid-state reaction technique is u ... s of the ceramics for the subsequent measurements.
780,10.1016/j.matchemphys.2010.03.056,solid_state_ceramic_synthesis,"La(1-x)/3NaxNbO3 (x = 0.04, 0.08, 0.12, 0.16, 0.20 ...  were muffled with powder of the same composition."
781,10.1016/j.matchemphys.2012.07.042,solid_state_ceramic_synthesis,Polycrystalline powders with the nominal compositi ... sity ~ 0.86 g cm-3) was used as the liquid medium.
782,10.1007/s10854-017-6712-1,solid_state_ceramic_synthesis,The polycrystalline sample of (Pb0.9Bi.05Y0.05) (F ... silver paste (highly conducting) for measurements.
783,10.1007/s10854-015-3654-3,solid_state_ceramic_synthesis,"Reagent grade Na2CO3, K2CO3, Nb2O5, Sb2O3, Bi2O3,  ... sealed alumina crucible to prevent volatilization."
784,10.1007/s10854-015-3021-4,solid_state_ceramic_synthesis,The samples involved in this study were synthesize ... ts were sintered at 1075-1200 degC for 4 h in air.
785,10.1016/j.ssc.2007.01.007,solid_state_ceramic_synthesis,"The solid state reaction method was used to prepar ... g/cm3, about 95% of the theoretical [30] and [32]."
786,10.1007/s10854-015-3768-7,solid_state_ceramic_synthesis,"High purity oxides such as Bi2O3 (99.9 %), TiO2 (9 ... ellets are around 97 % of the theoretical density."
787,10.1016/j.jeurceramsoc.2010.05.023,solid_state_ceramic_synthesis,BaCe0.95Y0.05O3-δ (BC5Y) powders were prepared by  ... s about 90% of the theoretical value (6310 kg/m3).
788,10.1016/j.electacta.2016.03.035,solid_state_ceramic_synthesis,Li2-xMgxNa2Ti6O14 (0.0 <= x <= 0.2) samples were s ... eve the final Li2-xMgxNa2Ti6O14 (0.0 <= x <= 0.2).
789,10.1016/j.matlet.2011.10.007,solid_state_ceramic_synthesis,The samples used in this study were prepared by th ... s were sintered at 1220/degC to 1260/degC for 3 h.
790,10.1007/s10854-012-0654-4,solid_state_ceramic_synthesis,The NiMn2O4 and La1-xCaxMnO3 (0 <= x <= 0.3) powde ... s ball-milled for 8 h again to break agglomerates.
791,10.1007/s10854-011-0574-8,solid_state_ceramic_synthesis,The raw materials used in this work were analytica ...  h. The heating rate was maintained at 100 degC/h.
792,10.1016/j.solidstatesciences.2009.09.015,solid_state_ceramic_synthesis,Ceramics with nominal composition of Bi2Sr2-xEuxCu ... he samples are furnace cooled to room temperature.
793,10.1016/j.jeurceramsoc.2008.08.028,solid_state_ceramic_synthesis,"The starting materials were Bi2O3 (Alfa Aesar, 99. ... w its sintering temperature to 125 degC for 5 min."
794,10.1007/s10854-015-3409-1,solid_state_ceramic_synthesis,The samples used in this study were synthesized by ... es ranging from 1300 to 1430 degC for 20 h in air.
795,10.1007/s10854-008-9674-5,solid_state_ceramic_synthesis,BNT and BiNbO4 powders were individually synthesiz ... emperature range of 1200-1320 degC for 2 h in air.
796,10.1016/j.matchemphys.2005.03.032,solid_state_ceramic_synthesis,Polycrystalline sample of Ba3La3Ti4NbO18 was prepa ... or 4 h to minimize the reduction of titanium ions.
797,10.1007/s10832-016-0030-5,solid_state_ceramic_synthesis,The conventional solid state reaction method was e ... mount of excess powder was about 5 g per crucible.
798,10.1016/j.ssi.2014.01.043,solid_state_ceramic_synthesis,The conventional solid state reaction method was e ... d sample names are denoted by LLZ400S and LLZ500S.
799,10.1016/j.mseb.2004.04.004,solid_state_ceramic_synthesis,"The powders were performed by the conventional sol ...  of 2 degC/min, prior to cooling with the furnace."
800,10.1016/j.materresbull.2012.01.009,solid_state_ceramic_synthesis,"(Na0.5K0.5)NbO3 + xCuTa2O6 samples (NKNCTx), where ... -1100 degC at a heating rate of 5 degC/min in air."
801,10.1016/j.jpowsour.2007.12.093,solid_state_ceramic_synthesis,LiFePO4 was prepared by the solid-state reaction o ... . All heating and cooling rates were 5 degC min-1.
802,10.1016/j.mseb.2008.12.029,solid_state_ceramic_synthesis,Mg2Si1-xSnx (0 <= x <= 1.0) solid solutions were s ... ples was more than 99.9% of the theoretical value.
803,10.1016/j.elecom.2012.10.037,solid_state_ceramic_synthesis,BaPr0.8In0.2O3 - δ (BPI) powder was prepared by th ... of ~ 8.7 mm in diameter and ~ 0.8 mm in thickness.
804,10.1007/s10854-014-1766-9,solid_state_ceramic_synthesis,"The CaCu3Ti4-xSbxO12 ceramics, where x = 0, 0.025, ... ce, and then cooled to room temperature naturally."
805,10.1016/j.electacta.2015.02.084,solid_state_ceramic_synthesis,Sm0.2Ce0.8O2-δ (SDC) electrolyte synthesized throu ...  200 MPa and sintered at 1550 degC in air for 4 h.
806,10.1016/j.tsf.2007.09.002,solid_state_ceramic_synthesis,"A commercial ferritic stainless steel (SUS430, 0.5 ... SF20 powders with the particle size of 100-125 μm."
807,10.1016/j.ceramint.2003.07.003,solid_state_ceramic_synthesis,Polycrystalline samples of PMN-PT (68:32) were pre ...  flat surfaces of the sintered and ground pellets.
808,10.1016/j.electacta.2015.05.008,solid_state_ceramic_synthesis,Pure lithium titanates were synthesized by solid-s ... ate for the volatilization of Li during synthesis.
809,10.1016/j.ceramint.2012.10.067,solid_state_ceramic_synthesis,"In the present work, Sr(Fe1-xHox)0.5Nb0.5O3 (SFHN) ... e pellet ceramics were measured using a LCR meter."
810,10.1016/j.matlet.2007.01.017,solid_state_ceramic_synthesis,The (1 - x)ZnAl2O4-xTiO2 powder compositions were  ... in up to 1000 degC and then it was furnace cooled.
811,10.1016/j.scriptamat.2016.01.003,solid_state_ceramic_synthesis,0.7CaTiO3-0.3NdAlO3 powders for SPS were prepared  ... 0 degC in oxygen to re-oxidize the Ti3 + to Ti4 +.
812,10.1016/j.ssi.2003.09.020,solid_state_ceramic_synthesis,"BaxCe0.8Er0.2O3-α (x=1.03, 1, 0.98) ceramics were  ... ectrolytes for the electrochemical determinations."
813,10.1016/j.matlet.2013.04.052,solid_state_ceramic_synthesis,(1-x)(K0.45Na0.51Li0.04)(Nb0.90Ta0.04Sb0.06)O3-xSr ... s of the ceramics were measured 24 h after poling.
814,10.1016/j.cattod.2004.04.059,solid_state_ceramic_synthesis,"LSCF powder was prepared by solid-state reaction.  ... h and 1473 K for 5 h, and then ground into powder."
815,10.1016/j.ssc.2012.02.025,solid_state_ceramic_synthesis,"BaBi1-xSbxO3 ceramics with x=0.0, 0.1, 0.2, 0.3, 0 ... me composition and sintered for 3 h in an O2 flow."
816,10.1007/s10008-010-1077-x,solid_state_ceramic_synthesis,LSGM electrolyte was used for the electrolyte in t ... red disk was polished to keep 0.5 mm in thickness.
817,10.1002/pssa.201026147,solid_state_ceramic_synthesis,(1 - x)BNKT15 -xBA (0 <= x <= 0.10) ceramics were  ... s with a diameter of 13 mm under 100 MPa pressure.
818,10.1016/j.ssi.2010.04.028,solid_state_ceramic_synthesis,GdBaCo2O5 + δ powers were prepared by a standard s ... en content was determined by iodometric titration.
819,10.1007/s10853-008-2946-x,solid_state_ceramic_synthesis,The Zn(ZrxTi1-x)O3 samples with x = 0-0.1 were pre ... sintered at temperatures of 800-950 degC for 24 h.
820,10.1111/j.1551-2916.2006.01181.x,solid_state_ceramic_synthesis,Li2Si2O5 was prepared by a conventional solid-stat ... ried at 85degC and then ground by an agate mortar.
821,10.1007/s10854-013-1113-6,solid_state_ceramic_synthesis,Polycristalline samples of Bi2Sr2Ca1Cu2-xNaxOy wit ...  start the formation of the superconducting phase.
822,10.1016/j.ssc.2005.11.040,solid_state_ceramic_synthesis,"(MgB2)2-xCux polycrystalline samples, with x=0.0,  ... heat treated at 925 degC for 2 h in Ar atmosphere."
823,10.1016/j.scriptamat.2006.07.040,solid_state_ceramic_synthesis,PZT/SiC composites were prepared by solid-state re ...  obtained in this study are summarized in Table 1.
824,10.1007/s10854-012-0993-1,solid_state_ceramic_synthesis,The designed compositions of PZT 95/5 ferroelectri ... treated at 700 degC for 20 min to form electrodes.
825,10.1016/j.jssc.2013.07.020,solid_state_ceramic_synthesis,A break-down approach by ball milling the pre-synt ... e product was calcined in air at 600 degC for 3 h.
826,10.1111/j.1551-2916.2009.03161.x,solid_state_ceramic_synthesis,"(1-x)La2/3TiO3-xLaAlO3 (with x=0.1), i.e. LaAlO3-s ... d to room temperature at rates of 900deg-15degC/h."
827,10.1016/j.electacta.2013.01.132,solid_state_ceramic_synthesis,Pristine LTO and LTO/AB/MWCNTs composites were pre ... e (10 degC min-1) to obtain well-crystallized LTO.
828,10.1016/j.matlet.2012.07.056,solid_state_ceramic_synthesis,Ce0.82La0.18O2-δ (LDC) added with 2.5 mol% V2O5 wa ... C without V2O5 addition was sintered at 1600 degC.
829,10.1111/j.1551-2916.2008.02585.x,solid_state_ceramic_synthesis,The compositions of (LixNb3x)Ti1-4xO2 were prepare ... s were sintered in air at 900deg-1170degC for 8 h.
830,10.1007/s10854-013-1376-y,solid_state_ceramic_synthesis,The conventional ceramic processing method was use ... tered ceramic samples for dielectric measurements.
831,10.1016/j.matlet.2007.03.021,solid_state_ceramic_synthesis,"Samples of (Zn1 - xAlxO)mIn2O3 (m = integer; x = 0 ... at 1823 K for 2 h in air, and then furnace cooled."
832,10.1016/j.jeurceramsoc.2017.04.058,solid_state_ceramic_synthesis,"The ceramics of composition BaCexTi1-xO3 (x = 0, 0 ... mples was measured employing Archimedes principle."
833,10.1007/s10853-012-6509-9,solid_state_ceramic_synthesis,"Nd(1 - x)/3MxNbO3 (M = Li, Ag; 0 <= x <= 0.20) cer ...  powders of the same composition during sintering."
834,10.1016/j.jeurceramsoc.2014.12.019,solid_state_ceramic_synthesis,The BT-PMN specimens were prepared by a solid-stat ... ith very good mechanical properties were obtained.
835,10.1016/j.ssi.2009.06.015,solid_state_ceramic_synthesis,"The powders of the Yb-doped BaZrO3 with the stoich ... dition and without the CuO addition, respectively."
836,10.1016/j.jpowsour.2011.04.047,solid_state_ceramic_synthesis,Li7La3Zr2O12 (LLZ) was prepared by a solid-state r ... flat surface and to control its thickness to 1 mm.
837,10.1016/j.jallcom.2009.03.187,solid_state_ceramic_synthesis,All the compositions of Co1-xNixFe1.9Mn0.1O4 (with ...  cooling was adopted for the both heat treatments.
838,10.1016/j.jeurceramsoc.2008.04.034,solid_state_ceramic_synthesis,"In this experiment, mixed powders of Ba0.5Sr0.5TiO ...  to the BST powder to lower sintering temperature."
839,10.1016/j.matlet.2016.11.066,solid_state_ceramic_synthesis,(Pb0.97La0.03)(Zr0.57Ti0.43)1-0.03/4O3(PLZT3/57/43 ...  pellets before electrical properties measurement.
840,10.1016/j.ssc.2007.03.032,solid_state_ceramic_synthesis,Both Pb0.96La0.04(Zr0.52Ti0.48)0.99O3 and Pb0.84La ... ure polycrystalline phase with no secondary phase.
841,10.1007/s10854-014-2228-0,solid_state_ceramic_synthesis,The samples of BSNTT were prepared from high purit ... degC in air for 3 h at heating rate of 5 degC/min.
842,10.1016/j.jeurceramsoc.2009.08.024,solid_state_ceramic_synthesis,CaCu3Ti4O12 ceramics were prepared using a solid s ... d silver paste to form a parallel plate capacitor.
843,10.1007/s10854-015-2775-z,solid_state_ceramic_synthesis,"Ceramic compositions of (1 - x)Pb(Zr0.53,Ti0.47)O3 ... ures (1,150, 1,175, 1,200 and 1,225 degC) for 2 h."
844,10.1016/j.jpowsour.2007.02.014,solid_state_ceramic_synthesis,The BIT powder used in this study was prepared by  ... .) was used as cathode throughout the experiments.
845,10.1016/j.matchemphys.2007.11.005,solid_state_ceramic_synthesis,"(Ba1-xLax)Zr0.2Ti0.8-x/4O3 (x = 0, 0.005, 0.01, 0. ... 2, 0.03 and 0.04 are corresponding to Samples A-F."
846,10.1007/s10832-007-9212-5,solid_state_ceramic_synthesis,Specimen powders were prepared by a conventional s ... ered at temperature 1350-1600 degC for 4 h in air.
847,10.1016/j.scriptamat.2012.03.022,solid_state_ceramic_synthesis,ST-BT composite ceramics were prepared by the conv ...  4294A impedance analyzer and a YE2730A d33 meter.
848,10.1007/s10854-016-4574-6,solid_state_ceramic_synthesis,Specimens of 5MgO-3Li2O-4WO3 ceramics were prepare ... in and then cooled to room temperature in furnace.
849,10.1016/j.matlet.2010.12.013,solid_state_ceramic_synthesis,BaCoIIxCoIII2xBi1 - 3xO3 powders with x = 0.0-0.1  ... as target material for thick-film paste formation.
850,10.1016/j.materresbull.2010.03.018,solid_state_ceramic_synthesis,Ceramic samples of La0.1Sr0.9-xDyxTiO3 with x = 0. ... mm) for measurements of thermoelectric properties.
851,10.1016/j.jpowsour.2013.11.026,solid_state_ceramic_synthesis,"BIT07 powder was synthesized by solid-state reacti ... P, the pore-forming agent, was provided by Timcal."
852,10.1007/s10854-009-9971-7,solid_state_ceramic_synthesis,K0.5Na0.5Nb0.92Sb0.08O3 + xmol%MnO2 ceramics (0 <= ... room temperature in a silicon oil bath for 30 min.
853,10.1016/j.matchemphys.2010.08.041,solid_state_ceramic_synthesis,BCTO ceramics were prepared by a conventional soli ... ith silver paint and fired at 575 degC for 20 min.
854,10.1016/j.jpowsour.2011.12.046,solid_state_ceramic_synthesis,LiMn0.8Fe0.19Mg0.01PO4 was synthesized by a solid- ... e carbon content of the product was around 8 wt.%.
855,10.1016/j.electacta.2006.05.006,solid_state_ceramic_synthesis,LSCM powders were prepared by conventional solid s ... lyte and in the composite mixtures was from Tosoh.
856,10.1016/j.matchemphys.2005.01.014,solid_state_ceramic_synthesis,"For the purpose of comparison, La(Mg1/2Ti1/2)O3 wa ... cined at 1200 and 1400 degC for 2 h in static air."
857,10.1016/j.matlet.2005.10.097,solid_state_ceramic_synthesis,Polycrystalline sample of Ba2La2TiNb2O12 was prepa ... or 4 h to minimize the reduction of titanium ions.
858,10.1016/j.matlet.2004.10.044,solid_state_ceramic_synthesis,Polycrystalline sample of Ba3La3Ti4NbO18 was prepa ... or 4 h to minimize the reduction of titanium ions.
859,10.1016/j.matlet.2016.04.174,solid_state_ceramic_synthesis,"(1-x)BaTiO3-xBiYO3 (x=0.00-0.30) ceramics, abbrevi ... he PVA, then sintered at 1300 degC for 2 h in air."
860,10.1016/j.jeurceramsoc.2009.06.037,solid_state_ceramic_synthesis,Perovskites in the system La0.2Sr0.8Fe1-xTixO3-δ ( ... e syntheses are marked as LSFT20_SP and LSFT40_SP.
861,10.1016/j.ssi.2010.04.009,solid_state_ceramic_synthesis,La2Mo2O9 powder was prepared by conventional solid ... on of 0.2%) than 95% of their theoretical density.
862,10.1016/j.materresbull.2007.02.018,solid_state_ceramic_synthesis,High-purity ZnO and SnO2 powders (Kojundo Chemical ... n air and then furnace-cooled to room temperature.
863,10.1007/s10853-014-8459-x,solid_state_ceramic_synthesis,CaMn1-yWyO3 (0 <= y <= 0.05) ceramics were prepare ... ed from the cell volume and the molecular formula.
864,10.1002/aenm.201400452,solid_state_ceramic_synthesis,"Synthesis: Re-substituted HMS, RexMn1-xSi1.8 (x =  ... k samples by SPS at 1123 K for 5 min under 60 MPa."
865,10.1016/j.msea.2008.10.054,solid_state_ceramic_synthesis,The elemental mixture of the above CNT-SiO2 compos ... rcements was used as a disk specimen of wear test.
866,10.1016/j.ceramint.2013.11.080,solid_state_ceramic_synthesis,The perovskite BaTiO3 ceramics specimens were prep ... ize was about 3-10 μm via atomic force microscope.
867,10.1111/j.1551-2916.2006.01236.x,solid_state_ceramic_synthesis,Compounds with nominal compositions Ca1-xZnxLa4Ti5 ... ize the effects of ZnO loss caused by evaporation.
868,10.1016/j.mseb.2015.05.009,solid_state_ceramic_synthesis,"A conventional mixed oxide method was utilized to  ... ore, well-densified ceramics were further studied."
869,10.1016/j.jpowsour.2012.06.101,solid_state_ceramic_synthesis,"La2O3 (99.99%), SrCO3 (99%), Ga2O3 (99.99%), MgO ( ...  at 1,400 degC for 4 h to get pure phase LSGM9182."
870,10.1016/j.ssi.2010.06.040,solid_state_ceramic_synthesis,Dy2Ti2O7 was prepared by solid-state reaction. A s ... n thickness and heat-treated at 1400 degC for 4 h.
871,10.1007/s10854-009-9913-4,solid_state_ceramic_synthesis,"Mn-doped BaZr0.2Ti0.8O3 ceramics (Mn content = 0,  ... i0.8O3 were sintered at 1,350 degC for 2 h in air."
872,10.1111/j.1551-2916.2005.00128.x,solid_state_ceramic_synthesis,The ceramics were prepared following a conventiona ... determined from weight and dimension measurements.
873,10.1016/j.jallcom.2012.12.117,solid_state_ceramic_synthesis,"In the current study, MgB2 added Bi1.8Pb0.4Sr2(MgB ...  M0, M1, M2, M3, M4, M5, M6 and Mn7, respectively."
874,10.1016/j.matchemphys.2008.11.021,solid_state_ceramic_synthesis,The pure composition K0.5La0.5Bi4Ti4O15 was produc ... amics were also produced under the same procedure.
875,10.1016/j.jeurceramsoc.2012.01.031,solid_state_ceramic_synthesis,LiMg(1-x)ZnxPO4 ceramics were prepared by the soli ... eratures were optimized for maximum densification.
876,10.1016/j.ceramint.2013.07.126,solid_state_ceramic_synthesis,"Reagent-grade SrCO3 (99%), TiO2 (98%), and Dy2O3 ( ... egC/min and furnace-cooled to ambient temperature."
877,10.1007/s10854-010-0136-5,solid_state_ceramic_synthesis,"Bi1.05-xDyxFeO3 (x = 0, 0.05, 0.1 and 0.2) ceramic ...  pasted with Ag paste on both sides as electrodes."
878,10.1016/j.mseb.2011.10.007,solid_state_ceramic_synthesis,The single-phase CCTO polycrystalline was prepared ... s the electrodes and fired at 600 degC for 30 min.
879,10.1016/j.mseb.2005.11.032,solid_state_ceramic_synthesis,"La1-xSrxCoO3 (x = 0, 0.1) samples were prepared by ... nd LSCO in the following discussion, respectively."
880,10.1002/ente.201500173,solid_state_ceramic_synthesis,(1-x)[0.94NBT-0.06BT]-xST ceramics were prepared u ...  of the disks and annealed at 500 degC for 30 min.
881,10.1016/j.matlet.2012.02.045,solid_state_ceramic_synthesis,A conventional solid-state reaction method was emp ...  compacts were sintered at 1250-1350 degC for 2 h.
882,10.1016/j.ceramint.2004.12.009,solid_state_ceramic_synthesis,"Ceramic samples of Sr1-1.5xYxTiO3, x <= 0.08 were  ... and 70% for x = 10, 30, and 50 wt.%, respectively."
883,10.1007/s10854-010-0119-6,solid_state_ceramic_synthesis,The ceramic samples are prepared by conventional s ... se was carried out at a rate of 5 degC per minute.
884,10.1016/j.ssi.2007.09.001,solid_state_ceramic_synthesis,La0.8Sr0.2Ga0.83Mg0.17O 2.815 (LSGM) was selected  ... ed to a thickness of 300 μm for single cell tests.
885,10.1007/s10854-014-2035-7,solid_state_ceramic_synthesis,"[Ba1-xSm2x/3](Zr0.05Ti0.95)O3 ceramics [x = 0, 0.0 ... ,100 degC for 4 h by using a programmable furnace."
886,10.1016/j.jallcom.2015.02.001,solid_state_ceramic_synthesis,BZCY powders were prepared by a conventional solid ... until a single perovskite-type phase was obtained.
887,10.1016/j.jpowsour.2013.10.105,solid_state_ceramic_synthesis,Powders of PrxCe0.95-xGd0.05O2-δ (PCGO) with x = 0 ... h a heating and cooling rate of 2 degC per minute.
888,10.1016/j.electacta.2011.01.121,solid_state_ceramic_synthesis,"A series of LiMn0.9Fe0.1-xMgxPO4/C (x = 0, 0.01, 0 ...  were heated at 800 degC under the same condition."
889,10.1016/j.jpowsour.2016.02.071,solid_state_ceramic_synthesis,The Pr1-xCaxBaCo2O5+δ (x = 0.1-0.4; PCBCO) double  ... ght ratio of 65:35 and used as the anode material.
890,10.1016/j.ssi.2005.09.027,solid_state_ceramic_synthesis,The samples were prepared by conventional solid st ... ing samples) or 1550 degC (Mn containing samples).
891,10.1016/j.jeurceramsoc.2011.03.036,solid_state_ceramic_synthesis,"LTA materials were synthesized by solid-state reac ...  MPa, followed by sintering at 1600 degC for 72 h."
892,10.1016/j.matlet.2015.09.110,solid_state_ceramic_synthesis,For the solid state reaction stoichiometric amount ... routes were sintered at 1500 degC for 24 h in air.
893,10.1002/pssa.201431289,solid_state_ceramic_synthesis,"Ba(Fe1-xGax)0.5Nb0.5O3 (BFGN) ceramics, where x =  ... e performed by using a LCR meter (Agilent E4980A)."
894,10.1016/j.matlet.2009.12.010,solid_state_ceramic_synthesis,BLTN-0.45 pellets used as PLD targets were prepare ... wish pellets were acquired through this procedure.
895,10.1016/j.electacta.2011.11.004,solid_state_ceramic_synthesis,"BaCe0.7In0.1A0.2O3-δ (A = Gd, Y) ceramics were syn ... stability after exposure to boiling water for 2 h."
896,10.1016/j.ssc.2009.06.041,solid_state_ceramic_synthesis,Na0.47K0.47Li0.06NbO3 ceramics were prepared by th ... he pellets were measured by the Archimedes method.
897,10.1007/s10854-012-0982-4,solid_state_ceramic_synthesis,"Li2ZnSiO4 ceramics were synthesized by the convent ... ts were sintered at 900-1,000 degC for 3 h in air."
898,10.1016/j.jallcom.2015.03.168,solid_state_ceramic_synthesis,BaZr0.85Y0.15O3-δ (BZY) powders were synthesized b ...  measured by the Archimedes' principle in ethanol.
899,10.1007/s10853-014-8599-z,solid_state_ceramic_synthesis,Ceramics with nominal composition (1 - x)Bi0.5(Na0 ... ly the pellets were sintered at 1150 degC for 4 h.
900,10.1016/j.matchemphys.2009.08.037,solid_state_ceramic_synthesis,Specimens of the Ba4Ti3P2O15 ceramics were prepare ... ts were sintered at 1150-1250 degC for 4 h in air.
901,10.1016/j.jallcom.2014.05.005,solid_state_ceramic_synthesis,Superconducting samples of type (ZnFe2O4)xGdBa2Cu3 ... ooled by a rate of 1 degC/min to room temperature.
902,10.1016/j.jssc.2004.08.005,solid_state_ceramic_synthesis,The ceramics were prepared using the conventional  ... re then sintered at 1225-1275 degC for 4 h in air.
903,10.1016/j.ssc.2004.09.006,solid_state_ceramic_synthesis,Samples were synthesized by a conventional solid-s ... the abbreviated expression represented in Table 1.
904,10.1016/j.elecom.2008.10.035,solid_state_ceramic_synthesis,"Samples of LBCFO and LBCCO were prepared using a s ... zed using a glycine-nitrate process, respectively."
905,10.1016/j.matlet.2012.12.053,solid_state_ceramic_synthesis,xBF-(1-x)(K0.5Bi0.5)TiO3 ceramics were prepared us ... r 2 hours in a powder bed of the same composition.
906,10.1016/j.mseb.2011.10.016,solid_state_ceramic_synthesis,Y0.08Sr0.92FexTi1-xO3-δ powder was synthesized by  ...  then wet and dry-milled in a planetary ball mill.
907,10.1007/s10854-011-0505-8,solid_state_ceramic_synthesis,"All samples Mn1.25Ni0.75Co1.0-xMgxO4 (x = 0, 0.1,  ... on. Silver wires were attached as electrode leads."
908,10.1016/j.jallcom.2013.07.005,solid_state_ceramic_synthesis,"Ca3-xSrxCo4O9 polycrystalline ceramic materials, w ... 0 degC for 24 h with a final furnace cooling [10]."
909,10.1111/j.1551-2916.2009.03060.x,solid_state_ceramic_synthesis,Sample of Mg2(Ti1-xSnx)O4 was synthesized by a con ... ctric properties were measured in this experiment.
910,10.1007/s10853-009-3285-2,solid_state_ceramic_synthesis,"La0.9Ba0.1Er1-xMgxO3-α (x = 0.05, 0.10, 0.15, 0.20 ... ectrolytes for the electrochemical determinations."
911,10.1007/s10854-011-0453-3,solid_state_ceramic_synthesis,CCTO ceramics were prepared by a solid state react ... densification (96-97% of the theoretical density).
912,10.1016/j.jeurceramsoc.2006.11.036,solid_state_ceramic_synthesis,The Ba3Ti5Nb6O28 powders were synthesized by conve ... 50 degC for 2 h with a heating rate of 5 degC/min.
913,10.1016/j.mseb.2005.12.028,solid_state_ceramic_synthesis,"In our experiment, ZnO-MgO pellets were prepared b ...  for 3 h and then cooled down to room temperature."
914,10.1016/j.scriptamat.2015.04.021,solid_state_ceramic_synthesis,Fine MgAlON ceramic powder with formula Mg0.27Al2. ... double surface polished to 2 and 0.5 mm thickness.
915,10.1016/j.mseb.2010.03.076,solid_state_ceramic_synthesis,Sodium lanthanum bismuth titanate piezoelectric ce ... amics were also produced under the same procedure.
916,10.1016/j.ssi.2003.12.042,solid_state_ceramic_synthesis,The SCY disks were prepared by solid state reactio ... etry was used to measure the density of the disks.
917,10.1016/j.jallcom.2009.02.049,solid_state_ceramic_synthesis,BaZr0.2Ti0.8O3 ceramics were prepared by solid-sta ... Pa pressure and sintered at 1350 degC for 0.5-8 h.
918,10.1016/j.matlet.2003.10.026,solid_state_ceramic_synthesis,Starting from simple carbonates and oxides of the  ... lysis was performed by FISEM with EDS (JSM-6700F).
919,10.1007/s10853-011-6185-1,solid_state_ceramic_synthesis,La3Ti2TaO11 samples were prepared by high-temperat ... 11 disks were then annealed at 1200 degC for 10 h.
920,10.1111/j.1744-7402.2008.02326.x,solid_state_ceramic_synthesis,Samples of (Mg0.95Ni0.05)TiO3 (MNT) and Ca0.6La0.8 ...  and the cooling rate were both set at 10degC/min.
921,10.1007/s10854-016-5505-2,solid_state_ceramic_synthesis,"Sr0.9((Na1-xKx)0.5Bi0.5)0.1Bi4Ti4O15 (x = 0.0, 0.1 ...  a sealed crucible by the ordinarily fired method."
922,10.1007/s10854-013-1409-6,solid_state_ceramic_synthesis,Conventional solid state reaction method was used  ... oom temperature in a silicone oil bath for 30 min.
923,10.1016/j.physb.2013.09.045,solid_state_ceramic_synthesis,"The manganite La0.7Ca0.3MnO3 was prepared by the c ...  into pellets, and sintered at 1350 degC for 24 h."
924,10.1016/j.jeurceramsoc.2015.09.033,solid_state_ceramic_synthesis,Li4WO5 ceramic was prepared by conventional solid  ... Li4WO5 compounds and sintered at 860 degC for 2 h.
925,10.1007/s10853-009-3779-y,solid_state_ceramic_synthesis,"BaTiO3 and NBT powders were individually synthesiz ...  disks were sintered at 1,150 degC for 2 h in air."
926,10.1016/j.jeurceramsoc.2007.02.172,solid_state_ceramic_synthesis,The nominal compositions of the PLZT samples prepa ... formed with wavelength ranging from 350 to 800 nm.
927,10.1016/j.jallcom.2015.01.090,solid_state_ceramic_synthesis,The produced materials 0.935Bi1/2Na1/2TiO3-0.065Ba ... into preprepared powder with the same composition.
928,10.1016/j.jeurceramsoc.2011.10.013,solid_state_ceramic_synthesis,The materials were prepared by the conventional so ... g the calcined powder with 50 wt% of AgNO3 powder.
929,10.1016/j.actamat.2014.03.002,solid_state_ceramic_synthesis,The Ni1-xZnxFe2O4 (0.0 x 0.7) ferrites were prepar ... oom temperature at a cooling rate of 4 degC min-1.
930,10.1016/j.mseb.2007.10.016,solid_state_ceramic_synthesis,Samples of MgTiO3 and CaTiO3 were individually syn ...  at temperatures of 1200-1350 degC for 4 h in air.
931,10.1016/j.jpowsour.2013.12.135,solid_state_ceramic_synthesis,"Li1+yMn1.5Ni0.5O4-xFx (0 <= x <= 0.5, 0 <= y <= 0. ... powder was heat treated in 800 degC for 12 h [32]."
932,10.1111/j.1744-7402.2009.02393.x,solid_state_ceramic_synthesis,"CaSiN2 and Ca1-xEuxAlzSiN2+z (x=0-0.02, z=0-0.3) w ... e of 0.48 MPa in a gas pressure-sintering furnace."
933,10.1007/s10854-015-3054-8,solid_state_ceramic_synthesis,"The (Ba0.85Ca0.15-xYx)(Zr0.1Ti0.9)O3(x = 0.00, 0.0 ... e disks were sintered at 1400 degC for 6 h in air."
934,10.1007/s10853-009-3915-8,solid_state_ceramic_synthesis,"The KNLN-BNBZT100x (x = 0, 0.01, 0.02, 0.03, 0.05, ... /mm at 110 degC in a silicone oil bath for 15 min."
935,10.1007/s00339-012-7443-z,solid_state_ceramic_synthesis,"The chemicals CaCO3 (99.98 %), CuO (99.5 %), MgO ( ... r 12 h for completion of the solid-state reaction."
936,10.1007/s10948-012-1968-4,solid_state_ceramic_synthesis,"Firstly, Bi2Sr2Ca2Cu3O10+δ powders were fabricated ... using an ultrasonic nebulizer operated at 2.4 MHz."
937,10.1007/s10854-016-5597-8,solid_state_ceramic_synthesis,The conventional solid-state reaction was used to  ... s were sintered in free-rich at 1200 degC for 2 h.
938,10.1016/j.mseb.2013.06.021,solid_state_ceramic_synthesis,Undoped ZnO pellets and ZnO-Sn2O3 composites were  ... rnace was closed to freeze slowly all the pellets.
939,10.1016/j.elecom.2011.11.009,solid_state_ceramic_synthesis,The Na3V2(PO4)3/C samples were synthesized by a on ... osphere. The reaction process is shown in Eq. (1).
940,10.1016/j.matchemphys.2013.11.015,solid_state_ceramic_synthesis,The (Pb1.06-xBax)(Nb0.94Ti0.06)2O6 (abbreviated as ... rs calcined at 1250 degC were denoted by PBNT/x-O.
941,10.1016/j.ceramint.2004.01.002,solid_state_ceramic_synthesis,The ZnTiO3 powders were prepared by conventional s ... sintered at temperatures of 800-940 degC for 24 h.
942,10.1016/j.ssc.2006.12.004,solid_state_ceramic_synthesis,Ceramics CaCu3Ti3.9O12 (CCTO39) and CCTO were prep ... ffractometer (D/MAX-RB) with the Cu K α radiation.
943,10.1016/j.jeurceramsoc.2006.11.029,solid_state_ceramic_synthesis,The Ba3Ti4Nb4O21 powders were synthesized by conve ... d samples was determined by the Archimedes method.
944,10.1016/j.jssc.2012.03.047,solid_state_ceramic_synthesis,"Powder samples of SrTa2O6 were prepared by convent ... gC for 20 h, and 1500 degC for 36 h, respectively."
945,10.1016/j.scriptamat.2012.04.042,solid_state_ceramic_synthesis,"YMn1-xTixO3 (0 x 0.25) powders were prepared by so ... degC for 5 and 10 h, depending on the composition."
946,10.1016/j.jallcom.2009.12.079,solid_state_ceramic_synthesis,(1 - x)(K0.5Na0.5)NbO3-xLi0.5Bi0.5TiO3 ceramics (K ... d 1170 degC using the ordinary firing (OF) method.
947,10.1016/j.jeurceramsoc.2016.05.021,solid_state_ceramic_synthesis,The substituted barium zirconates BaCe0.5Zr0.4Y0.1 ... ers were milled again for 24 h as described above.
948,10.1016/j.ssi.2013.09.010,solid_state_ceramic_synthesis,Starting powders of La0.6Sr0.4Co0.2Fe0.8O3 - δ wer ... s of 1250 degC (for the LSCF) or 1350 degC (PLNO).
949,10.1016/j.ssi.2015.02.005,solid_state_ceramic_synthesis,"PLD targets of SrZrO3 (SZO), SrZr0.95Y0.05O3 (SZY) ...  be sintered at 1600 degC for 10 h in ambient air."
950,10.1016/j.fuel.2014.06.017,solid_state_ceramic_synthesis,"To synthesize pure perovskites via the SSR method, ... d have been reported in our previous studies [33]."
951,10.1016/j.matchemphys.2009.07.051,solid_state_ceramic_synthesis,Samples of Bi4HfxV2-xO11-(x/2)-δ for 0 <= x <= 0.4 ... h and gradually cooled in air to room temperature.
952,10.1007/s10854-008-9809-8,solid_state_ceramic_synthesis,The polycrystalline sample of Nd3/2Bi3/2Fe5O12 (NB ... 150 degC before making any electrical measurement.
953,10.1007/s10854-013-1247-6,solid_state_ceramic_synthesis,The samples used in this study were prepared by th ...  degC) for 4 h at the normal atmospheric pressure.
954,10.1016/j.enconman.2010.05.013,solid_state_ceramic_synthesis,La0.8Sr0.2MnO3 specimens were prepared via solid-s ...  times. The detailed flow sheet is seen in Fig. 1.
955,10.1016/j.jnucmat.2014.10.025,solid_state_ceramic_synthesis,"(Gd,A)2(Zr,B)2O7 ceramics were prepared via a soli ... tes were 5 degC per minute in the sintering steps."
956,10.1016/j.cej.2009.07.009,solid_state_ceramic_synthesis,p-Type CaFe2O4 powders were prepared by the conven ... re wine in color under the preparation conditions.
957,10.1016/j.jssc.2004.11.017,solid_state_ceramic_synthesis,The CuAlO2 sample was prepared by a solid-state re ... ed at 1100 degC for 24 h and quench cooled in air.
958,10.1016/j.jallcom.2004.11.066,solid_state_ceramic_synthesis,The samples were prepared by solid-state reaction  ...  by an X-ray diffractometer using Cu Kα radiation.
959,10.1016/j.jeurceramsoc.2016.05.017,solid_state_ceramic_synthesis,"Ag(Nb1-xTax)O3 ceramics with x = 0, 0.2, 0.35, 0.5 ... hensive comparison of their functional properties."
960,10.1016/j.jmmm.2011.02.048,solid_state_ceramic_synthesis,The (1-x)Pb[Zr0.23Ti0.36+0.02(Mg1/2W1/2)+0.39(Ni1/ ... ric field of 1.5 kV/mm for 30 min in silicone oil.
961,10.1007/s10854-015-3988-x,solid_state_ceramic_synthesis,KNN-LS-BF-ZnO ceramics were prepared by convention ...  80 degC for 15 min under a dc field of 3.5 kV/mm.
962,10.1007/s10800-008-9745-6,solid_state_ceramic_synthesis,"Polycrystalline BaCe0.9-xZrxY0.1O3-δ powders (x =  ... h and then calcined at 1,400 degC for 24 h in air."
963,10.1016/j.jmmm.2012.04.017,solid_state_ceramic_synthesis,"Polycrystalline samples of La0,67Ba0,33Mn0,9Cr0,1O ... nd cooled down to room temperature in the furnace."
964,10.1016/j.ssi.2004.10.005,solid_state_ceramic_synthesis,The Li2xCa0.5-xTaO3 compounds were prepared by sol ...  pellets were quenched to room temperature in air.
965,10.1016/j.jlumin.2011.10.021,sol_gel_ceramic_synthesis,"By sol-gel method, a series of red-emitting phosph ... e bought from Sinopharm Chemical Reagent Co., Ltd."
966,10.1016/j.optmat.2003.11.009,sol_gel_ceramic_synthesis,Rare-earth doped yttrium aluminum garnet samples w ... dditionally sintered for 10 h at 1000 degC in air.
967,10.1007/s10853-009-4123-2,sol_gel_ceramic_synthesis,"Red-emitting phosphors, Sr2Ca1-2xEuxNaxMoO6 (x = 0 ... s for 8 h in air to get the white phosphor powder."
968,10.1016/j.matchemphys.2013.09.017,sol_gel_ceramic_synthesis,The sol-gel combustion method was employed for pre ... oxides also were prepared through the same method.
969,10.1002/cplu.201300235,sol_gel_ceramic_synthesis,Nanosized Li2CoTi3O8 powder was synthesized by mea ... or 4 h in air to obtain the pure Li2CoTi3O8 phase.
970,10.1007/s10854-010-0090-2,sol_gel_ceramic_synthesis,"0.67PMN-0.33PT powders were prepared through an aq ... /min, yellow 0.67PMN-0.33PT powders were obtained."
971,10.1016/j.jeurceramsoc.2014.12.010,sol_gel_ceramic_synthesis,xBa(Zr0.2Ti0.8)O3-(1-x)(Ba0.7Ca0.3)TiO3 (0.48 <= x ... ation. The synthesis procedure is shown in Fig. 1.
972,10.1016/j.ijhydene.2014.07.051,sol_gel_ceramic_synthesis,The Pr0.83BaCo1.33Sc0.5O6-δ-0.17PrCoO3 (PBCS-0.17P ... chematic synthesis procedures are shown in Fig. 1.
973,10.1016/j.mssp.2015.01.021,sol_gel_ceramic_synthesis,LiCr0.33V0.33Mn0.33O2 powder was produced via sol- ... 7 h in air in order to eliminate organic contents.
974,10.1016/j.ceramint.2003.12.178,sol_gel_ceramic_synthesis,"Nanostructured barium hexaferrite powders were syn ... are named in with A1, A2, A3 and A4, respectively."
975,10.1016/j.renene.2008.04.021,sol_gel_ceramic_synthesis,"A series of Ni-Ti-Zr metal oxides with various Ti: ... enoted as Ni5TixZr5 - x (x = 0, 1, 2.5, 4, and 5)."
976,10.1016/j.ssi.2010.01.017,sol_gel_ceramic_synthesis,Cobalt doped Sm0.95Ce0.05FeO3 - δ powders were pre ... 0 degC for 24 h to form the perovskite structures.
977,10.1016/j.mseb.2011.07.012,sol_gel_ceramic_synthesis,The (1-x)BiFeO3-x(Bi0.5Na0.5)TiO3 (x = 0 - 0.6) so ... essed into pellets and sintered at 1223 K for 3 h.
978,10.1016/j.jssc.2012.08.003,sol_gel_ceramic_synthesis,"Undoped and 1% mol (with respect to the alkaline i ...  the doped ones as NN:Ln and NKN:Ln, respectively."
979,10.1016/j.ssi.2012.01.036,sol_gel_ceramic_synthesis,The Li3V2(PO4)3 coating solution was prepared by a ... 4/C@Li3V2(PO4)3/C composite material was obtained.
980,10.1016/j.jmmm.2015.09.044,sol_gel_ceramic_synthesis,"The Ni0.8Zn0.2LaxFe2-xO4 (where x=0, 0.02, 0.06 an ... 800 degC for 2 h to form the Ni0.8Zn0.2LaxFe2-xO4."
981,10.1007/s10008-012-1970-6,sol_gel_ceramic_synthesis,Layered Li[Li0.2Mn0.54Ni0.13Co0.13]O2 (labeled as  ... obtain the pristine Li[Li0.2Mn0.54Ni0.13Co0.13]O2.
982,10.1016/j.ssc.2009.06.019,sol_gel_ceramic_synthesis,"Li3V 2(PO4)3-xFx ( x = 0 , 0.05 , 0.10 , 0.15 ) ca ... ed at 700 [?]C for 10 h under an inert atmosphere."
983,10.1007/s11581-008-0265-5,sol_gel_ceramic_synthesis,"The LiMxMn2 - xO4 (M=Li, Fe, Co; x = 0, 0.05, 0.1, ... and then calcined at 600-800 degC for 24 h in air."
984,10.1016/j.jpowsour.2009.03.044,sol_gel_ceramic_synthesis,Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF) perovskite oxide w ... n the products with the desired lattice structure.
985,10.1016/j.snb.2015.04.048,sol_gel_ceramic_synthesis,The Co3V2O8 was prepared from cobalt chloride hexa ... ffle furnace by a gradual increase of temperature.
986,10.1016/j.electacta.2011.04.131,sol_gel_ceramic_synthesis,LiMn2O4 powders were synthesized by a sol-gel meth ... he pristine material in the following experiments.
987,10.1016/j.materresbull.2007.03.023,sol_gel_ceramic_synthesis,A solid reaction method and a sol-gel method were  ... alcined at 900 degC for 10 h to turn into product.
988,10.1016/j.optmat.2011.01.019,sol_gel_ceramic_synthesis,"Sr3(VO4)2, Sr2Y2/3-yEuy(VO4)2, Y1-xEuxVO4 and Sr2Y ... d into pellets and sintered at 1000 degC for 10 h."
989,10.1016/j.ijhydene.2010.01.079,sol_gel_ceramic_synthesis,"The GdBaCo2 - xNixO5 + δ (GBCO, GBCN, x = 0~0.3) p ... degC in air for 5 h to obtain the desired powders."
990,10.1016/j.ssc.2008.06.040,sol_gel_ceramic_synthesis,Nanocrystalline powder of CoFe2O4 were prepared by ... tely at 570 [?]C for 4 h to get the final product.
991,10.1007/s10854-014-2256-9,sol_gel_ceramic_synthesis,The Bi2Fe4O9 powders were synthesized by a sol-gel ... peratures to obtain the Co doped Bi2Fe4O9 powders.
992,10.1016/j.jpowsour.2011.10.066,sol_gel_ceramic_synthesis,The starting materials used in the experiment were ...  24 h in air and then cooling to room temperature.
993,10.1016/j.materresbull.2015.08.015,sol_gel_ceramic_synthesis,"Bi0.95Nd0.05Fe1-xNixO3 (x = 0, 0.01, 0.03 and 0.05 ... eO3 samples and used for further characterization."
994,10.1016/j.electacta.2015.01.145,sol_gel_ceramic_synthesis,Pristine LMNO was synthesized by a sol-gel method  ... t 870 degC for 10 h to obtain the target material.
995,10.1016/j.jpowsour.2005.10.015,sol_gel_ceramic_synthesis,Cathode materials were prepared by the sol-gel met ... and heated at 950 degC for 12 h and then quenched.
996,10.1016/j.jpowsour.2015.03.054,sol_gel_ceramic_synthesis,0.5Li2MnO3-0.5LiNi0.33Co0.33Mn0.33O2 powder was sy ... 5 h in air to obtain the desired cathode material.
997,10.1016/j.jpowsour.2006.05.042,sol_gel_ceramic_synthesis,"In addition, two spinel phases LiMn2O4 are indepen ... ooling and grinding procedures at 750 degC in air."
998,10.1016/j.synthmet.2009.02.026,sol_gel_ceramic_synthesis,The samples of LiMn2O4 spinel were prepared by the ... n air for 10 h to obtain the final spinel product.
999,10.1002/pssb.201451753,sol_gel_ceramic_synthesis,Samples are prepared by sol-gel method via a nitra ... in air to obtain a light-gray colored fine powder.
1000,10.1016/j.jelechem.2014.01.033,sol_gel_ceramic_synthesis,Pristine CuCrO2 was prepared by a sol-gel method u ... ution. The molar ratio of AgNO3 to CuCrO2 was 1:5.
1001,10.1016/j.electacta.2013.07.020,sol_gel_ceramic_synthesis,The bare layered oxide Li[Li0.2Mn0.56Ni0.16Co0.08] ... ormed layered oxide Li[Li0.2Mn0.56Ni0.16Co0.08]O2.
1002,10.1016/j.ssi.2010.12.010,sol_gel_ceramic_synthesis,Precursors for the nominal chemical formula Li7La3 ...  the mother powder for high temperature annealing.
1003,10.1016/j.jpowsour.2005.12.095,sol_gel_ceramic_synthesis,"Al-F co-substituted Li[Ni0.333Co0.333Mn0.293Al0.04 ... r 18 h, followed by quenching to room temperature."
1004,10.1007/s10854-014-2120-y,sol_gel_ceramic_synthesis,"YVO4:Eu3+ nanophosphors were prepared by a sol-gel ... o 1,000 degC for 4 h to prepare the nanophosphors."
1005,10.1016/j.jpowsour.2008.11.045,sol_gel_ceramic_synthesis,Both PrBC oxide and SDC oxide powders were synthes ...  final product with the desired lattice structure.
1006,10.1016/j.jmmm.2016.02.048,sol_gel_ceramic_synthesis,"The samples of Bi1-xGdxFeO3 (x=0, 0.05, and 0.1) w ... Gd0.05FeO3 (BG5FO), and Bi0.90Gd0.10FeO3 (BG10FO)."
1007,10.1016/j.jpowsour.2007.11.062,sol_gel_ceramic_synthesis,Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF) oxide was used as  ... in the final product with the desired composition.
1008,10.1016/j.matlet.2014.11.129,sol_gel_ceramic_synthesis,Li3V2(PO4)3/C composite was prepared through a fac ...  h under Ar flow to yield Li3V2(PO4)3/C composite.
1009,10.1016/j.matlet.2012.01.025,sol_gel_ceramic_synthesis,"The Bi1/2Na1/2Cu3Ti4O12 (BNCTO) samples were prepa ... egC, 900 degC, 950 degC and 1000 degC for 3 hours."
1010,10.1016/j.solidstatesciences.2015.12.001,sol_gel_ceramic_synthesis,Low temperature synthesis (sol-gel method) was als ...  further calcined at 700-750 degC in air for 12 h.
1011,10.1007/s10854-015-3361-0,sol_gel_ceramic_synthesis,"Ca(NO3)2*4H2O (A.R.), KNO3 (A.R.), (NH4)2HPO4 (A.R ... :Eu3+ phosphor is prepared according to Ref. [25]."
1012,10.1016/j.cattod.2014.06.042,sol_gel_ceramic_synthesis,The pechini sol-gel method (P) was applied after m ... ial was then calcined in air at 600 degC for 10 h.
1013,10.1016/j.jpowsour.2009.11.041,sol_gel_ceramic_synthesis,"LiNi0.33-xMn0.33Co0.33AlxO2 (x = 0, 0.01) material ...  cooled slowly in the furnace to room temperature."
1014,10.1016/j.apsusc.2009.10.105,sol_gel_ceramic_synthesis,"LiFePO4 powder samples were prepared by a sol-gel  ... r carbon content, which was of about a 10% weight."
1015,10.1016/j.jpcs.2005.11.002,sol_gel_ceramic_synthesis,"In this study, compounds of general formula Ce6MoO ... emperatures in air and cooled to room temperature."
1016,10.1016/j.jpowsour.2006.02.005,sol_gel_ceramic_synthesis,LiAl1/3-xCoxNi1/3Mn1/3O2 compounds were synthesize ...  were slowly cooled to room temperature in oxygen.
1017,10.1016/j.jphotochem.2004.05.018,sol_gel_ceramic_synthesis,Zinc ferrite doped titania powder was prepared by  ... ichiometric proportion of zinc ferrite to titania.
1018,10.1016/j.jssc.2008.01.031,sol_gel_ceramic_synthesis,N-Ce codoped nano-TiO2 photocatalysts were synthes ... ed the nominal atomic ratio of cerium to titanium.
1019,10.1016/j.jallcom.2014.03.138,sol_gel_ceramic_synthesis,Cathode powder PrBa0.5Sr0.5CoCuO5+δ was synthesize ... as prepared by glycine-nitrate combustion process.
1020,10.1016/j.ijhydene.2013.06.047,sol_gel_ceramic_synthesis,Ba0.5Sr0.5Co0.8Fe0.2O3 (BSCF) powders were prepare ... ized and then calcined at 900 degC for 4 h in air.
1021,10.1016/j.apcatb.2017.02.074,sol_gel_ceramic_synthesis,A series of Bi2O3-Co3O4 catalysts were prepared by ...  Co3O4 and Bi2O3 were obtained by the same method.
1022,10.1016/j.jpowsour.2008.04.019,sol_gel_ceramic_synthesis,"Unmodified LiMn2O4 powders were prepared by the so ... C for 24 h, followed by grinding in an agate bowl."
1023,10.1016/j.jpowsour.2008.06.021,sol_gel_ceramic_synthesis,All the raw materials applied in this study were p ... 00 degC for 5 h in air to give the final products.
1024,10.1016/j.jpowsour.2013.01.064,sol_gel_ceramic_synthesis,PrBa0.5Sr0.5Co2-xFexO5+δ (PBSCF) series samples (x ... ground and finally sintered at 1000 degC for 10 h.
1025,10.1016/j.jallcom.2006.01.054,sol_gel_ceramic_synthesis,The samples of spinel lithium manganese oxide were ... n air for 10 h to obtain the final spinel product.
1026,10.1016/j.matlet.2006.01.083,sol_gel_ceramic_synthesis,"Sr2MWO6 (M = Co, Ni) were prepared in polycrystall ... l heat treatment was at 1200 degC for 20 h in air."
1027,10.1016/j.jallcom.2010.04.076,sol_gel_ceramic_synthesis,"To prepare LiCr0.1Ni0.4Mn1.5O4 material, a sol-gel ... calcined at 900 degC for 8 h to turn into product."
1028,10.1016/j.ijhydene.2015.07.104,sol_gel_ceramic_synthesis,Polycrystalline dual-phase powders were prepared v ... eat treatment according to characterization items.
1029,10.1016/j.ijhydene.2013.05.022,sol_gel_ceramic_synthesis,The iron oxide based catalysts promoted with alumi ... l nitrates during the preparation of the catalyst.
1030,10.1016/j.ssc.2011.04.009,sol_gel_ceramic_synthesis,A series of polycrystalline samples of Ca3Co4-xMox ... ck ceramic pellets of Ca3Co4-xMoxO9 were obtained.
1031,10.1007/s10008-008-0628-x,sol_gel_ceramic_synthesis,The samples of LiNi0.5Mn1.5O4 and LiMn1.4Cr0.2Ni0. ... or 20 h in air to obtain the final spinel product.
1032,10.1007/s10853-010-4569-2,sol_gel_ceramic_synthesis,Nanocrystalline La1-xCoxMn1-yNiyO3 (x = 0.2 and 0. ... n order to improve the crystallinity of materials.
1033,10.1007/s10854-015-3840-3,sol_gel_ceramic_synthesis,A series of Tb2-xEux(MoO4)3 nanophosphors with var ... lowish white powders of Tb2-xEux(MoO4)3 phosphors.
1034,10.1016/j.apsusc.2015.08.039,sol_gel_ceramic_synthesis,The precursors (molar ratio: Cu/Zn/Al = 2/1/0.8) w ... anded with three heat treatment ways as following:
1035,10.1016/j.cattod.2012.04.036,sol_gel_ceramic_synthesis,"A series of LaCo1-xMnxO3 (x = 0.05, 0.1, 0.3, 0.5, ...  calcinated at 700 degC for 4 h in muffle roaster."
1036,10.1016/j.tsf.2011.07.001,sol_gel_ceramic_synthesis,"LiMn2O4 powder prepared by the sol-gel method, Li( ... n at 850 degC for 15 h to get pure LiMn2O4 powder."
1037,10.1016/j.jallcom.2008.06.102,sol_gel_ceramic_synthesis,The samples were prepared by the nitrate-citrate s ... trate to citrate used in the present work was 1:1.
1038,10.1016/j.jallcom.2006.07.058,sol_gel_ceramic_synthesis,A sol-gel process was used to prepare the ZnO-coat ... r 6 h at 500 degC to obtain the ZnO-coated spinel.
1039,10.1016/j.apsusc.2010.02.085,sol_gel_ceramic_synthesis,Co-doped TiO2 anatase nanoparticles were prepared  ... l was then dried and calcined at 500 degC for 5 h.
1040,10.1016/j.jpowsour.2008.10.055,sol_gel_ceramic_synthesis,BSCF powders were synthesized by a combined EDTA-c ... degC for 5 h in air to produce the final products.
1041,10.1016/j.jmmm.2012.02.110,sol_gel_ceramic_synthesis,"Yttrium nitrate, ferric nitrate, and cobalt nitrat ... emperatures (300, 600, 900 and 1200 degC) for 1 h."
1042,10.1016/j.mssp.2014.07.041,sol_gel_ceramic_synthesis,"Bi1-xBaxFeO3 (x=0 and 0.15) nanoparticles were pre ... a 4), 550 degC (Ba 5) and 650 degC (Ba 6) for 4 h."
1043,10.1016/j.ssi.2006.03.055,sol_gel_ceramic_synthesis,LiNi1/3Mn1/3Co1/3O2 compounds were synthesized by  ... at 450 degC for 5 h and then at 900 degC for 15 h.
1044,10.1007/s10854-015-2743-7,sol_gel_ceramic_synthesis,"(1 - x)BFO/xNFO composite powders (with x = 10, 20 ... mosphere to obtain the LBFO/NFO composite powders."
1045,10.1016/j.optmat.2010.10.049,sol_gel_ceramic_synthesis,"Yb3+/Er3+ codoped BaGd2(MoO4)4 powder samples were ... te method at 1273 K, as reported in the Ref. [13]."
1046,10.1002/celc.201600718,sol_gel_ceramic_synthesis,Pr0.5Ba0.5CoO3-δ (PBC) powder was synthesised by u ... lise the perovskite structure on the final powder.
1047,10.1016/j.matchemphys.2008.05.055,sol_gel_ceramic_synthesis,BST35 and BST50 powder and ceramics were prepared  ... ered at 1320 degC for 5 h and cooled in a furnace.
1048,10.1016/j.snb.2008.02.033,sol_gel_ceramic_synthesis,The La1-xMgxFeO3 powders were prepared by a sol-ge ... raction (XRD) to determine the phase constituents.
1049,10.1016/j.jelechem.2008.09.007,sol_gel_ceramic_synthesis,"LiMn2O4 powder was prepared by the sol-gel method, ... nation at 850 degC for 15 h to get LiMn2O4 powder."
1050,10.1016/j.jpowsour.2007.06.120,sol_gel_ceramic_synthesis,"Three samples, LiMn2O4, LiCr0.16Mn1.84O4 and LiCr0 ... he samples. All the chemicals were analytic grade."
1051,10.1016/j.jallcom.2016.05.138,sol_gel_ceramic_synthesis,The precursors used for the synthesis of Bi0.95Yb0 ... al products are used for further characterization.
1052,10.1016/j.mseb.2014.05.012,sol_gel_ceramic_synthesis,"Polycrystalline samples of BFO, BEFO, BEFMO and BE ... hermal treatment at 250 and 550 degC both for 2 h."
1053,10.1016/j.matchemphys.2016.05.042,sol_gel_ceramic_synthesis,The xPr3+:NGW (x = 0.5-5 mol% in steps of 0.5) pho ...  air atmosphere at 800 degC for 2 h [35] and [36].
1054,10.1016/j.apsusc.2012.12.019,sol_gel_ceramic_synthesis,Zr4+ doped TiO2 nanoparticles with different volum ... equently the product was crushed into fine powder.
1055,10.1002/jctb.4409,sol_gel_ceramic_synthesis,The synthesis of spinel ferrites having compositio ...  400degC and 1000degC for 2 h in a muffle furnace.
1056,10.1016/j.ssi.2011.08.003,sol_gel_ceramic_synthesis,La0.6Sr0.4Fe0.8Cu0.2O3-δ (LSFCu) catalyst was synt ... of 5 degC min-1 to obtain a single phase of LSFCu.
1057,10.1016/j.jpowsour.2005.03.167,sol_gel_ceramic_synthesis,Li[(CoNi1/2Mn1/2)x(Li1/3Mn2/3)(1-2x)]O2 precursor  ... t the temperature range of 950 degC in atmosphere.
1058,10.1016/j.ssi.2004.11.018,sol_gel_ceramic_synthesis,The Sr- or Ce-doped PrMnO3 oxides were prepared by ...  degC for 1 h and calcination at 750 degC for 3 h.
1059,10.1016/j.ssc.2011.11.009,sol_gel_ceramic_synthesis,"The samples were prepared via the citrate sol-gel  ... ly, the dry gel was calcined at 1000 degC for 1 h."
1060,10.1016/j.jpowsour.2008.05.052,sol_gel_ceramic_synthesis,Pr1-xSrxCo0.8Fe0.2O3-δ (x = 0.2-0.6) powders were  ... the sol-gel method and firing at 600 degC for 4 h.
1061,10.1007/s10008-005-0042-6,sol_gel_ceramic_synthesis,"Nano-structured ion doped ceria, yttrium doped cer ... e calcined powders were ground completely for use."
1062,10.1016/j.jpowsour.2012.05.070,sol_gel_ceramic_synthesis,"Sm0.5-xBaxSr0.5Co0.8Fe0.2O3-δ (x = 0, 0.05, 0.10,  ...  final product with the desired lattice structure."
1063,10.1016/j.ssi.2003.08.003,sol_gel_ceramic_synthesis,Li[Li0.1Ni0.35-x/2CoxMn0.55-x/2]O2 (x=0-0.3) compo ... 50 degC for 20 h and quenched to room temperature.
1064,10.1016/j.electacta.2014.08.043,sol_gel_ceramic_synthesis,"Bare LiMn2O4 powders were synthesized via a sol-ge ...  and then, the pure LiMn2O4 powders were obtained."
1065,10.1016/j.matlet.2003.07.025,sol_gel_ceramic_synthesis,The NBT powders were prepared by a sol-gel method. ... btained was then annealed for 2 h at 500-700 degC.
1066,10.1016/j.jpowsour.2013.09.049,sol_gel_ceramic_synthesis,"Sr2Fe1.5Mo0.5-xTaxO6-δ (SFMTO, 0.0 <= x <= 0.15) w ... l-gel method as described elsewhere [20] and [21]."
1067,10.1016/j.matchemphys.2007.04.073,sol_gel_ceramic_synthesis,Spinel LiMn2O4 were prepared by a citric acid assi ...  degC for 12 h before cooling to room temperature.
1068,10.1007/s10854-015-2795-8,sol_gel_ceramic_synthesis,The sol-gel method was used to prepare the CCTO po ... d at 700 degC for 10 h to form the CCTO particles.
1069,10.1016/j.physe.2015.01.010,sol_gel_ceramic_synthesis,"Mn doped YCrO3 [YCr1-xMnxO3 (YCrMnO) with x=0, 0.0 ... sor powder is calcined in air at 800 degC for 1 h."
1070,10.1016/j.matlet.2010.01.043,sol_gel_ceramic_synthesis,BaFe12O19 particles were prepared by a citrate sol ... -burnt powders were calcined at 1000 degC for 2 h.
1071,10.1002/adfm.201400436,sol_gel_ceramic_synthesis,Sample Preparation: Li1.2Ni0.13Co0.13Mn0.54(BO4)0. ... n at 850 degC for 15 h to get the target products.
1072,10.1016/j.jpowsour.2010.02.063,sol_gel_ceramic_synthesis,LiMn1.5Ni0.5O4 was synthesized by a sol-gel method ... lting precursor was annealed at 850 degC for 15 h.
1073,10.1016/j.electacta.2008.01.058,sol_gel_ceramic_synthesis,BSCF powders were synthesized by a combined EDTA-c ... degC for 5 h in air to produce the final products.
1074,10.1016/j.physb.2010.03.039,sol_gel_ceramic_synthesis,BaFe12O19 particles were prepared by a citrate sol ... s-burnt powders were calcined at 900 degC for 2 h.
1075,10.1016/j.nanoen.2015.11.015,sol_gel_ceramic_synthesis,"In the second step, 15 mol% Ca2+ doped SDC was pre ... ed at 750 degC for 2 h to obtain the SCDC product."
1076,10.1016/j.electacta.2013.11.023,sol_gel_ceramic_synthesis,"LiZnxNi0.5-xMn1.5O4 (x = 0, 0.02, 0.04, 0.08, 0.25 ...  and finally sintered at 850 degC for 24 h in air."
1077,10.1016/j.jlumin.2012.12.011,sol_gel_ceramic_synthesis,Mn-doped TiO2 nanoparticles with nominal Mn (x) co ...  h to get crystalline Mn-doped TiO2 nanoparticles.
1078,10.1016/j.jpowsour.2010.07.022,sol_gel_ceramic_synthesis,"For comparison, LiV3O8 was prepared by sol-gel met ... cined at 500 degC for 8 h and LiV3O8 was obtained."
1079,10.1016/j.apsusc.2015.02.085,sol_gel_ceramic_synthesis,"In case of samples prepared by sol-gel method glyc ... r this process, the calcined powders became white."
1080,10.1016/j.jpowsour.2008.05.053,sol_gel_ceramic_synthesis,LSSMy composite oxides (y = 0.0-0.2) were synthesi ... air atmosphere to yield the final desired product.
1081,10.1016/j.ssi.2007.04.012,sol_gel_ceramic_synthesis,"Li[Ni1/3Co1/3Mn1/3]1-xRexO2(Re = La, Ce, Pr) was s ... f rare earth elements was evaluated by ICP method."
1082,10.1016/j.electacta.2016.01.066,sol_gel_ceramic_synthesis,Al-substituted Li[Li0.2Ni0.15Mn0.55Co0.1-xAlx]O2 ( ... ets at 850 degC for 6 h and then 900 degC for 6 h.
1083,10.1016/j.matchemphys.2012.10.016,sol_gel_ceramic_synthesis,Co-doped MgAl2O4 nanoparticles with the compositio ...  the desired temperatures (600-1000 degC) for 5 h.
1084,10.1016/j.jnoncrysol.2005.05.024,sol_gel_ceramic_synthesis,Co2+:LiAl5O8 nanocrystals were synthesized via a c ... nk fluffy product was obtained after the reaction.
1085,10.1016/j.materresbull.2014.06.001,sol_gel_ceramic_synthesis,The catalysts were prepared by the sol-gel method. ... repared with the same procedure as spinel MgCr2O4.
1086,10.1016/j.optmat.2010.09.018,sol_gel_ceramic_synthesis,The Eu3+-doped InVO4 phosphors formulated (In1-xEu ... obtained were calcined at 950 degC in air for 6 h.
1087,10.1007/s10800-015-0798-z,sol_gel_ceramic_synthesis,Perovskite powders were synthesized using the sol- ... MO3 perovskites were pulverized once more [18-20].
1088,10.1016/j.matlet.2012.08.126,sol_gel_ceramic_synthesis,The as-prepared LiNi0.5Mn1.5O4 was synthesized via ... n annealing treatment at 650 degC for 10 h in air.
1089,10.1016/j.elecom.2011.06.031,sol_gel_ceramic_synthesis,"Li[Li0.2Co0.4Mn0.4]O2 was prepared by a sol-gel me ... or 15 h, followed by quenching in liquid nitrogen."
1090,10.1016/j.apcatb.2014.10.044,sol_gel_ceramic_synthesis,"The CoCr2O4 catalysts were prepared with a sol-gel ... O4-x, with x referring to calcination temperature."
1091,10.1016/j.jallcom.2013.09.117,sol_gel_ceramic_synthesis,"Polycrystalline samples BFO, BiFe0.95Co0.05O3 (BFC ... gC for 2 h, and then sintered at 600 degC for 2 h."
1092,10.1016/j.ijhydene.2015.07.126,sol_gel_ceramic_synthesis,La0.2Sr0.7TiO3 powder was prepared by a convention ... ed at 750 degC for 4 h to obtain the final powder.
1093,10.1016/j.spmi.2015.09.010,sol_gel_ceramic_synthesis,"The spinel structure FeCo2O4 materials were synthe ... lly, the powder was sintered at 900 degC for 12 h."
1094,10.1016/j.matchemphys.2009.08.059,sol_gel_ceramic_synthesis,A series of acetate-tartrate gel precursor samples ... n a flowing oxygen atmosphere at ambient pressure.
1095,10.1007/s10853-012-6758-7,sol_gel_ceramic_synthesis,"La1-xSrxFeO3 (x = 0.0-1.0) materials were prepared ... y, the precursor was calcined at 650 degC for 6 h."
1096,10.1016/j.jpcs.2006.01.067,sol_gel_ceramic_synthesis,LiCoO2 precursor was prepared by sol-gel method us ... t 850 degC for 6 h to obtain the LiCoO2 precursor.
1097,10.1016/j.jnoncrysol.2008.06.112,sol_gel_ceramic_synthesis,La0.8Sr0.2MnO3 samples were prepared by using the  ... as formed which was decomposed at 300 degC in air.
1098,10.1016/j.electacta.2010.08.016,sol_gel_ceramic_synthesis,LiMn2O4 powder was prepared by the sol-gel method. ... n at 850 degC for 15 h to get pure LiMn2O4 powder.
1099,10.1016/j.jpowsour.2009.10.016,sol_gel_ceramic_synthesis,La1-xSrxCoO3 (x = 0.1-0.5) perovskite oxides were  ... n air in order to form La1-xSrxCoO3 (x = 0.1-0.5).
1100,10.1016/j.mee.2015.07.007,sol_gel_ceramic_synthesis,"The (La3 +, Pr3 +) ion co-doped InVO4 phosphors we ... obtained were calcined at 950 degC in air for 6 h."
1101,10.1016/j.jpowsour.2014.02.013,sol_gel_ceramic_synthesis,A complexing sol-gel process was used for the synt ... 3-δ (BCY-non) and Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF).
1102,10.1016/j.optmat.2014.12.038,sol_gel_ceramic_synthesis,"The Tb2-xSmx(MoO4)3 (x = 0.001, 0.0014, 0.002, 0.0 ...  to get yellowish white powder of Tb2-xSmx(MoO4)3."
1103,10.1016/j.cattod.2010.08.023,sol_gel_ceramic_synthesis,TiO2 was obtained by the sol-gel method using tita ... 0 degC during 4 h at a heating rate of 2 degC/min.
1104,10.1016/j.electacta.2010.12.049,sol_gel_ceramic_synthesis,The Li[Li0.2Mn0.54Ni0.13Co0.13]O2 material was pre ... red by sol-gel method is indicated as SG-material.
1105,10.1016/j.apcatb.2008.08.009,sol_gel_ceramic_synthesis,"MnOx-CeO2 mixed oxides, MnOx and CeO2 were prepare ...  MnOx-CeO2 is denoted as MnOx(X)-CeO2 in the text."
1106,10.1016/j.electacta.2011.05.007,sol_gel_ceramic_synthesis,Lithium-ion-conducting material LATP was synthesiz ... d then sieved through a #325 mesh for further use.
1107,10.1016/j.electacta.2010.08.022,sol_gel_ceramic_synthesis,"LiNi0.33-xMn0.33Co0.33YxO2 (x = 0, 0.025, 0.05, 0. ... for 5 h then calcined at 850 degC for 16 h in air."
1108,10.1016/j.jpowsour.2007.06.151,sol_gel_ceramic_synthesis,LiMn0.5Ni0.5O2 powders were synthesized by the sol ...  to obtain the ZrO2-coated LiMn0.5Ni0.5O2 powders.
1109,10.1016/j.jallcom.2016.02.090,sol_gel_ceramic_synthesis,Synthesis by the sol-gel method [43]: The starting ... 00 degC for 12 h to remove the organic components.
1110,10.1016/j.materresbull.2004.12.002,sol_gel_ceramic_synthesis,The Y-Ga-O gel was prepared using stoichiometric a ... -gel synthesis of the Y3Ga5O12 is shown in Fig. 1.
1111,10.1016/j.cattod.2016.05.015,sol_gel_ceramic_synthesis,A series of perovskite-type La0.8K0.2Co1-yMnyO3(y  ... en calcined at 700 degC for 5 h in muffle roaster.
1112,10.1016/j.jallcom.2015.01.123,sol_gel_ceramic_synthesis,"The samples of Bi1-xLaxFeO3 (0 x 0.50) were synthe ... gC for 2 h, the final power samples were prepared."
1113,10.1016/j.jpowsour.2012.11.099,sol_gel_ceramic_synthesis,Li[Li0.2Co0.13Ni0.13Mn0.54]O2 powder was prepared  ... The reaction scheme can be represented as follows:
1114,10.1016/j.ssc.2006.09.002,sol_gel_ceramic_synthesis,"Polycrystalline La0.8-xNdxNa0.2MnO3 ( x = 0.00 , 0 ... ined in air at 1473 K for 10 h and furnace cooled."
1115,10.1007/s10008-014-2708-4,sol_gel_ceramic_synthesis,The LiMn1.90Mg0.05Si0.05O4 cathode materials were  ... n2O4 sample was synthesized by the same technique.
1116,10.1016/j.ijhydene.2012.07.031,sol_gel_ceramic_synthesis,Powders of BSCF and Sm0.2Ce0.8O1.9 (SDC) were prep ... al calcination temperature was set to be 800 degC.
1117,10.1016/j.jallcom.2008.06.157,sol_gel_ceramic_synthesis,The LiCoxMn2-xO4 powder was synthesized by the sol ... perature rising rate was maintained at 1 degC/min.
1118,10.1016/j.ssc.2006.03.001,sol_gel_ceramic_synthesis,"Polycrystalline La0.67Ca0.33Mn1-xO3 (x=0.00, 0.02, ... ined in air at 1273 K for 10 h and furnace cooled."
1119,10.1016/j.cej.2008.11.046,sol_gel_ceramic_synthesis,The catalysts were prepared by the sol-gel method. ...  nickel mass content is about 17% measured by AAS.
1120,10.1016/j.tsf.2014.10.074,sol_gel_ceramic_synthesis,La0.6Ca0.4Fe0.8Ni0.2O3 - δ (LCFN) were synthesized ... on of a gel. The product was sintered at 800 degC.
1121,10.1016/j.optmat.2014.10.050,sol_gel_ceramic_synthesis,Nano-garnets of Lu3(1-x)Ho3xGa5O12 and Y3(1-x)Ho3x ... ts using Y(NO3)3[?]4H2O instead of Lu(NO3)3[?]H2O.
1122,10.1016/j.physb.2009.09.081,sol_gel_ceramic_synthesis,The compound oxide powders in the following system ... s during calcination were maintained 1 degC min-1.
1123,10.1016/j.jssc.2005.01.022,sol_gel_ceramic_synthesis,The LaNiO3 perovskite precursors in this work were ... us a transparent and homogeneous sol was obtained.
1124,10.1016/j.mssp.2013.07.016,sol_gel_ceramic_synthesis,The synthesis of calcium ferrite nanoparticles was ... alcium ferrite nanoparticles as the final product.
1125,10.1016/j.snb.2012.07.011,sol_gel_ceramic_synthesis,Zinc and manganese (II) acetates were used as prec ... anopowders can be found in our previous work [10].
1126,10.1007/s10562-014-1268-7,sol_gel_ceramic_synthesis,The various MnOx were prepared by sol-gel and prec ... muffle. The obtained catalyst is denoted as Mn-SG.
1127,10.1016/j.renene.2016.01.073,sol_gel_ceramic_synthesis,"The reagents used were Mn(NO3)2*4H2O (Merck), KNO3 ... re crushed and sieved with desired particle sizes."
1128,10.1016/j.apcata.2009.03.019,sol_gel_ceramic_synthesis,"Bulk perovskites: LaMnO3, La0.9Sr0.1MnO3 and LaMn1 ... tion was grinded and calcined at 850 degC for 2 h."
1129,10.1016/j.jpowsour.2010.02.080,sol_gel_ceramic_synthesis,SDC oxide powder was synthesized by a combined EDT ... final products with the desired lattice structure.
1130,10.1016/j.ijhydene.2014.04.203,sol_gel_ceramic_synthesis,S1-xBCO oxides with various Sm3+-deficiencies of x ... asured by Archimedes method to be higher than 95%.
1131,10.1016/j.jmmm.2011.06.026,sol_gel_ceramic_synthesis,"Nanocrystalline powders of NiFe2-xAlxO4 (x=0, 0.5, ... 2 h in air to get the final single phase products."
1132,10.1016/j.elecom.2005.11.010,sol_gel_ceramic_synthesis,The synthesis of Li2MnSiO4 or Li2FeSiO4 was carrie ... l. The sol was dried at 60 degC for at least 24 h.
1133,10.1016/j.jpowsour.2013.04.005,sol_gel_ceramic_synthesis,Layered-perovskite oxides LaBa1-xCo2O5+δ (LB1-xCO) ... 150 degC for 4 h to study their phase stabilities.
1134,10.1016/j.cattod.2009.05.028,sol_gel_ceramic_synthesis,"The studied perovskite-type oxides LaNiO3, La0.8Ca ...  for 24 h and calcined in air at 700 degC for 5 h."
1135,10.1016/j.jmmm.2011.07.016,sol_gel_ceramic_synthesis,The chemicals used for the synthesis of different  ... material was naturally cooled to room temperature.
1136,10.1016/j.jmmm.2016.07.058,sol_gel_ceramic_synthesis,The synthesis of Gd-Co and Nd-Co substituted bariu ...  at the rate of 23 degC/min to obtain hexaferrite.
1137,10.1016/j.jallcom.2013.02.129,sol_gel_ceramic_synthesis,"Ferrite nanoparticles of basic composition Ni0.7-x ... present, and then finally ground for half an hour."
1138,10.1016/j.electacta.2012.06.115,sol_gel_ceramic_synthesis,Li0.35La0.55TiO3 (LLTO) was synthesized by sol-gel ... or gelation and then calcined at 900 degC for 6 h.
1139,10.1016/j.jallcom.2006.11.059,sol_gel_ceramic_synthesis,"The composites of BaFe12O19 and TiO2 were prepared ... at 850 degC, the composites were obtained finally."
1140,10.1016/j.matlet.2011.12.005,sol_gel_ceramic_synthesis,A sol-gel method [13] and [16] was employed to syn ... egC for 5 h. The final product was a white powder.
1141,10.1016/j.electacta.2013.10.211,sol_gel_ceramic_synthesis,The nominal composition of P2-Na0.67NixFe0.35-xMn0 ... air atmosphere for obtaining phase pure materials.
1142,10.1016/j.jallcom.2012.09.142,sol_gel_ceramic_synthesis,La and Pr co-substituted Bi1-x-yLaxPryFeO3 (BLPFO) ...  were immediately removed from the furnace to air.
1143,10.1016/j.jpowsour.2012.03.019,sol_gel_ceramic_synthesis,"Oxide powders, including BSCF and SSC electrode ma ... final product with the targeted phase composition."
1144,10.1007/s10008-014-2534-8,sol_gel_ceramic_synthesis,Layered perovskite PrBaCo2 - xNixO5 + δ oxide powd ...  degC for 5 h in air to yield the desired powders.
1145,10.1007/s10853-006-0077-9,sol_gel_ceramic_synthesis,"In this work we investigate the influence of the h ... d and treated at 800 degC for 1, 2, 4, 8 and 16 h."
1146,10.1007/s10854-013-1414-9,sol_gel_ceramic_synthesis,"Pure and Tb-doped BiFeO3 nanoparticles were prepar ... 0), 550 degC (Tb550) and 650 degC (Tb650) for 4 h."
1147,10.1002/celc.201300026,sol_gel_ceramic_synthesis,P2-Na0.66Fe0.5Mn0.5O2 was prepared by using the so ... C in air for 15 h to obtain P2-Na0.66Fe0.5Mn0.5O2.
1148,10.1016/j.jeurceramsoc.2010.01.008,sol_gel_ceramic_synthesis,"Na2CO3 (99.8%), K2CO3 (99%), citric acid (C6H8O7*H ... te of 5 degC/min to obtain NKN nano-sized powders."
1149,10.1016/j.jallcom.2015.10.250,sol_gel_ceramic_synthesis,"Bi1-xGdxFe1-yCoyO3 (x = 0.00, 0.05, y = 0.00, 0.05 ... O3 (G5C5), and Bi0.95Gd0.05Fe0.90Co0.10O3 (G5C10)."
1150,10.1016/j.ssc.2011.02.014,sol_gel_ceramic_synthesis,BiFeO3 (BFO) and BiFe0.9Cr0.1O3 (BFCO) compound sp ... g in order to investigate the electric properties.
1151,10.1007/s10854-015-3522-1,sol_gel_ceramic_synthesis,"Gd3-xAl5O12:xBi3+(x = 0.005, 0.01, 0.03, 0.045, 0. ... powders were calcined for 3 h at 1300 degC in air."
1152,10.1016/j.optmat.2007.05.021,sol_gel_ceramic_synthesis,Lu2O3 powders doped or co-doped with 0.2 mol% Sm2O ... nd the corresponding crystalline powders resulted.
1153,10.1016/j.jpowsour.2010.12.036,sol_gel_ceramic_synthesis,Sm0.2Ce0.8O1.9 (SDC) powder was prepared using sol ... ubjected to calcination at different temperatures.
1154,10.1007/s00706-009-0205-8,sol_gel_ceramic_synthesis,TiO2 nanoparticles were prepared by the sol-gel me ... h to obtain TiO2 nanoparticles of different sizes.
1155,10.1016/j.mseb.2010.04.036,sol_gel_ceramic_synthesis,"SrTiO3 photocatalyst was prepared by citrate sol-g ...  at 383 K, the gel was calcined at 823 K for 12 h."
1156,10.1016/j.jpowsour.2014.04.068,sol_gel_ceramic_synthesis,The sample of 0.4Li2MnO3*0.6LiNi1/3Co1/3Mn1/3O2 (L ... recursor was annealed in air at 900 degC for 24 h.
1157,10.1016/j.optmat.2017.02.034,sol_gel_ceramic_synthesis,The citrate sol-gel method was used to synthesis t ... or different time periods (varying from 1 to 6 h).
1158,10.1016/j.jpowsour.2012.01.034,sol_gel_ceramic_synthesis,Double layered perovskite oxides PB1-xCO with Ba-d ...  in air for study of their chemical compatibility.
1159,10.1016/j.electacta.2011.06.019,sol_gel_ceramic_synthesis,"LiFePO4/C was prepared from ferric citrate, ammoni ... ithium acetate (CH3COOLi*2H2O) as precursors [26]."
1160,10.1002/cctc.201500966,sol_gel_ceramic_synthesis,"The BaMeO3 (Me=Mn, Co, Fe) mixed oxides were prepa ... for 2 h, and finally calcined at 700 degC for 4 h."
1161,10.1007/s10854-015-3259-x,sol_gel_ceramic_synthesis,"Zn1-xNixAl2O4 (x = 0, 0.025, 0.05, 0.075, 0.10) na ... ered at 700 degC for 6 h to prepare Zn1-xNixAl2O4."
1162,10.1016/j.optmat.2006.05.016,sol_gel_ceramic_synthesis,YAG powder used as the starting material for nanoc ... sample was calcinated at 900 degC in air for 16 h.
1163,10.1016/j.electacta.2013.10.091,sol_gel_ceramic_synthesis,The Li-rich layered Li[Li0.2Mn0.54Ni0.13Co0.13]O2  ... . The reaction scheme can be listed as follow [8].
1164,10.1016/j.cattod.2013.02.019,sol_gel_ceramic_synthesis,"The catalyst Ni-CZsol-gel was synthesized by a pse ... degC for 6 h, with a heating ramp of 2 degC min-1."
1165,10.1016/j.matlet.2012.07.110,sol_gel_ceramic_synthesis,The pure LiNi0.5Mn1.5O4 was synthesized by a sol-g ... y annealing treatment at 650 degC for 10 h in air.
1166,10.1016/j.jpowsour.2013.09.042,sol_gel_ceramic_synthesis,BaZr0.1Ce0.7Y0.1Yb0.1O3 (BZCYYb) powders were prep ... l. The gel was then calcined at 1000 degC for 5 h.
1167,10.1016/j.jmmm.2012.06.042,sol_gel_ceramic_synthesis,The Mn-Zn ferrite powders (Mn0.8Zn0.2Fe2O4) were p ...  acetone and stirred until the acetone evaporated.
1168,10.1016/j.electacta.2010.04.033,sol_gel_ceramic_synthesis,LiNi0.1Mn0.1Co0.8O2 oxide was prepared using the s ... ultimate annealing at 900 degC for 12 h under air.
1169,10.1016/j.jpcs.2015.01.009,sol_gel_ceramic_synthesis,Mn-doped ZnGa2O4 nanoparticles with the compositio ... o the desired temperatures (600-900deg C) for 5 h.
1170,10.1016/j.matchemphys.2013.06.049,sol_gel_ceramic_synthesis,The LiCoO2 particles were synthesized by the sol-g ... 0 degC for 24 h to yield the final LiCoO2 product.
1171,10.1016/j.jpowsour.2015.06.022,sol_gel_ceramic_synthesis,LSM regular particles were also synthesized throug ... ized and then calcined at 700 degC for 4 h in air.
1172,10.1016/j.jpowsour.2005.03.166,sol_gel_ceramic_synthesis,Nano-sized LiNi0.45Mn0.45Co0.1O2 powders were synt ... oling rate of the heat treatment was 2 degC min-1.
1173,10.1016/j.jssc.2013.10.019,sol_gel_ceramic_synthesis,ZnAl2O4:Ti powders were prepared by a sol-gel meth ... fects of doping on the structure and luminescence.
1174,10.1016/j.electacta.2012.05.096,sol_gel_ceramic_synthesis,The as-prepared LiNi0.475Al0.01Cr0.04Mn1.475O3.95F ... thod without adding the substituted raw materials.
1175,10.1016/j.physleta.2010.08.045,sol_gel_ceramic_synthesis,"The samples of BiFe1 - xCrxO3 ( x = 0 , 0.05 and 0 ... g in order to investigate the electric properties."
1176,10.1016/j.jmmm.2013.08.054,sol_gel_ceramic_synthesis,Nanoparticles ferrites have been synthesized by th ... ers are cooled down to room temperature naturally.
1177,10.1007/s10854-014-2054-4,sol_gel_ceramic_synthesis,BBT powders and gel precursors were prepared by so ...  for 1 h (300 degC) and 2 h (800 degC) at furnace.
1178,10.1016/j.ijhydene.2015.09.091,sol_gel_ceramic_synthesis,"Sm0.5Sr0.5CoO3-δ (SSC), Ba(Co0.7Fe0.2Nb0.1)O3-δ (B ...  SSC and BCFN powder was prepared in similar ways."
1179,10.1016/j.jlumin.2011.08.020,sol_gel_ceramic_synthesis,The preparation of cobalt doped TiO2 nanoparticles ... o get the desired cobalt doped TiO2 nanoparticles.
1180,10.1016/j.jpcs.2011.10.021,sol_gel_ceramic_synthesis,The nanoparticles of Bi0.9-xLa0.1CaxFeO3 (BLCFOx)  ... ated samples were annealed at 650 degC for 30 min.
1181,10.1016/j.optmat.2014.04.018,sol_gel_ceramic_synthesis,LGNPs were synthesized by a pechini sol-gel method ... e heated at the temperature range of 700-900 degC.
1182,10.1016/j.optmat.2010.04.030,sol_gel_ceramic_synthesis,"Sr3V2-xPxO8 (0 x 2), Sr2.7Eu0.2V2-yPyO8 (0 y 2) an ... 800, and 1000 degC to obtain the phosphor samples."
1183,10.1016/j.jnoncrysol.2007.06.013,sol_gel_ceramic_synthesis,The Y4Al2O9 were synthesized by normal sol-gel met ... o 1000 degC in a muffle furnace in air atmosphere.
1184,10.1016/j.ssi.2013.08.010,sol_gel_ceramic_synthesis,In this work LiMn2O4 powders have been synthesized ... ange of 450 - 700 degC at a rate of 5 degC min- 1.
1185,10.1016/j.jallcom.2008.11.099,sol_gel_ceramic_synthesis,BaTiO3 powders (~200 nm) were synthesized by sol-g ... mperature facilitated to tetrahedron BaTiO3 phase.
1186,10.1016/j.mssp.2012.02.002,sol_gel_ceramic_synthesis,Appropriate proportions of high purity zinc acetat ...  by placing pellets in a ceramic boat at 400 degC.
1187,10.1016/j.jallcom.2014.04.130,sol_gel_ceramic_synthesis,The Zn0.2Mn0.8Fe2O4 nanoparticles were prepared by ... or 5 h. The sample will be denoted as ZnMn ferrite
1188,10.1016/j.chemphys.2006.04.007,sol_gel_ceramic_synthesis,The YBa2Cu4O8 superconducting samples were prepare ... re with intermediate regrinding and repelletizing.
1189,10.1016/j.optmat.2015.01.021,sol_gel_ceramic_synthesis,"To study down-shifting of the phosphors, BaGd2ZnO5 ...  (x = 0, 1, 5) were prepared with the same method."
1190,10.1016/j.mssp.2014.08.032,sol_gel_ceramic_synthesis,RE (RE=Eu and Nd) doped ZnFe2O4 nanoparticles were ... rocess only without adding Eu3+ and Nd3+ solution.
1191,10.1007/s10008-013-2014-6,sol_gel_ceramic_synthesis,The LiCoO2 particles were synthesized by the sol-g ... 0 degC for 24 h to yield the final LiCoO2 product.
1192,10.1016/j.jpowsour.2009.11.029,sol_gel_ceramic_synthesis,The sol-gel method was used to coat ZrP2O7 on the  ... ting powder was heated at 400 degC for 6 h in air.
1193,10.1016/j.matchemphys.2012.12.064,sol_gel_ceramic_synthesis,The LSMO nanoparticles were prepared by the tradit ... etails of preparation process are shown in Fig. 1.
1194,10.1016/j.mseb.2005.06.018,sol_gel_ceramic_synthesis,Sn1-xMgxO2-δ:Eu phosphors were synthesized by a mo ... % and this value was checked by chemical analysis.
1195,10.1016/j.jallcom.2010.04.203,sol_gel_ceramic_synthesis,SrFe12O19 particles were prepared by a citrate sol ... s-burnt powders were calcined at 900 degC for 2 h.
1196,10.1016/j.cattod.2010.04.019,sol_gel_ceramic_synthesis,"Ce-La-O mixed oxides, La2O3 and CeO2 were prepared ...  ratios (X) are denoted as Ce(X)-La-O in the text."
1197,10.1016/j.matlet.2005.03.024,sol_gel_ceramic_synthesis,LTNO particles were prepared by the sol-gel method ... ed into fine particles with sizes of about 1.0 μm.
1198,10.1016/j.ssc.2007.04.027,sol_gel_ceramic_synthesis,The polycrystalline bulk and nanosized samples of  ... ooling to produce the polycrystalline bulk sample.
1199,10.1016/j.jpowsour.2005.03.079,sol_gel_ceramic_synthesis,Layered LiNixCo1-2xMnxO2 (1/3 <= x <= 1/2) powders ...  cooling rate was maintained as 2 degC per minute.
1200,10.1016/j.jpowsour.2013.01.167,sol_gel_ceramic_synthesis,The NASICON-type LAGP powder was prepared using a  ... 00 degC for 5 h to complete the chemical reaction.
1201,10.1016/j.cattod.2005.07.073,sol_gel_ceramic_synthesis,"The studied mixed-oxide perovskites LaFeO3, LaFe0. ...  for 24 h and calcined in air at 700 degC for 5 h."
1202,10.1007/s10008-007-0325-1,sol_gel_ceramic_synthesis,"All the chemical reagents used in the experiments  ... h, followed by slowly cooling to room temperature."
1203,10.1007/s10854-015-3081-5,sol_gel_ceramic_synthesis,BiFeO3 ceramics were prepared via sol-gel method.  ...  h to obtain well crystallized BFO nano-particles.
1204,10.1016/j.apenergy.2017.03.131,sol_gel_ceramic_synthesis,The CaO/Ca3Al2O6 sorbents with varying mass ratios ... te the performance of the as-synthesized sorbents.
1205,10.1016/j.ssi.2010.03.020,sol_gel_ceramic_synthesis,"Three Nasicon type compositions, Ca0.5Fe1 - xEuxSb ... ps are shown in the form of a flow chart (Fig. 1)."
1206,10.1007/s10934-015-9932-x,sol_gel_ceramic_synthesis,Cobalt ferrite nanopowders were synthesized by a P ... egC for one hour by a heating rate of 10 degC/min.
1207,10.1016/j.ssc.2010.05.035,sol_gel_ceramic_synthesis,"Ce3+, Tb3+ co-doped CaAl2SiO6 phosphors were prepa ... here of 5%H2-95%N2 gas to get the final phosphors."
1208,10.1016/j.physb.2013.01.015,sol_gel_ceramic_synthesis,"Ni-Zn ferrite of composition ZnxNi1-xFe2O4 (x=0.0, ... egC for 2 h to carry out further characterization."
1209,10.1016/j.jmmm.2016.03.085,sol_gel_ceramic_synthesis,"Bi1-xGdxFe1-xTixO3 (for x=0.05, 0.1, 0.15 and 0.20 ... n for 4 h to acquire the fine crystalline product."
1210,10.1016/j.cej.2015.05.121,sol_gel_ceramic_synthesis,CuFe2O4 was synthesized with a sol-gel combustion  ... hed with pure water and dried at 50 degC for 48 h.
1211,10.1016/j.optmat.2015.03.053,sol_gel_ceramic_synthesis,"First method (TiO2:Fe 1%, TiO2:Fe 5%, TiO2:Fe 10%) ...  TiO2:Fe x% powder was heated at 500 degC for 1 h."
1212,10.1016/j.jpowsour.2005.03.094,sol_gel_ceramic_synthesis,Li0.99Al0.01FePO4 samples were synthesized by a so ... The heating rate of the furnace was 10 degC min-1.
1213,10.1016/j.ijhydene.2014.03.179,sol_gel_ceramic_synthesis,A series of ceria-substituted on the A-sites of La ... THERM) at 1373 K for 5 h to form the black powder.
1214,10.1016/j.snb.2015.07.023,sol_gel_ceramic_synthesis,The Zn3V2O8 was prepared from zinc nitrate hexahyd ... o the procedure previously described in Ref. [13].
1215,10.1007/s10854-015-3974-3,sol_gel_ceramic_synthesis,Cerium doped gadolinium gallium garnet (Gd3-xCexGa ... ere further sintered in air at 1000 degC for 10 h.
1216,10.1016/j.jssc.2008.03.010,sol_gel_ceramic_synthesis,"Several samples were prepared by solid-state react ...  in air for 72-120 h, with intermediate grindings."
1217,10.1016/j.jpowsour.2007.03.041,sol_gel_ceramic_synthesis,Phase-pure BSCF and LC oxide powders were synthesi ...  at 900 degC for 5 h to obtain the final products.
1218,10.1002/cssc.201500143,sol_gel_ceramic_synthesis,Li[Li0.2Ni0.17Co0.07Mn0.56]O2 powder was synthesiz ... gC for 12 h in air to afford the target compounds.
1219,10.1007/s10800-013-0632-4,sol_gel_ceramic_synthesis,The LiMn2O4 powders were produced using a well-kno ... before being calcined at 300 degC for 24 h in air.
1220,10.1016/j.ssi.2006.02.001,sol_gel_ceramic_synthesis,Ca2Mn3O8 was prepared by a sol-gel method from Mn( ... heated to 750 degC for 5 h under a flow of O2 gas.
1221,10.1016/j.electacta.2015.02.027,sol_gel_ceramic_synthesis,LiMn2O4 coated with LSM composite material was pre ...  by LSM are denoted as BLMO and LLMO respectively.
1222,10.1016/j.matlet.2010.10.087,sol_gel_ceramic_synthesis,Perovskite ZnSnO3 nanoparticles were prepared by a ... tment of the precursor at 700 degC for 3 h in air.
1223,10.1016/j.electacta.2014.07.103,sol_gel_ceramic_synthesis,"To synthesize the spinel LTO/C composite, we basic ... he calcination was performed under air atmosphere."
1224,10.1016/j.ijhydene.2010.08.077,sol_gel_ceramic_synthesis,The Ce0.8Sm0.2O1.9 (SDC) powder was synthesized vi ... oroughly for the subsequent preparation procedure.
1225,10.1007/s10854-016-4999-y,sol_gel_ceramic_synthesis,ZnNiCr-ferrite particles were prepared by a simpli ... rogrammed furnace to get the required cubic phase.
1226,10.1016/j.apsusc.2014.06.196,sol_gel_ceramic_synthesis,"The CeO2 support was prepared using a sol-gel meth ... ight, followed by calcination at 500 degC for 4 h."
1227,10.1016/j.matchemphys.2016.02.058,sol_gel_ceramic_synthesis,"To synthesize NFO/BTO nanorods, a sol-gel process  ... on was subjected to annealing at 650 degC for 3 h."
1228,10.1016/j.jmmm.2012.11.010,sol_gel_ceramic_synthesis,BaTiO3 nano-particles were prepared by the sol-gel ...  800 degC for 2 h to obtain BaTiO3 nano-particles.
1229,10.1016/j.elecom.2013.05.022,sol_gel_ceramic_synthesis,LiNi0.5Mn1.5O4 was prepared by sol-gel method. C6H ... 0 degC for 2 h in air to obtain the final product.
1230,10.1016/j.jpowsour.2016.04.087,sol_gel_ceramic_synthesis,Li(Ni0.5Co0.5)1-yFeyO2 (0.0 <= y <= 0.25) samples  ... roducts were sintered at 800 degC in air for 24 h.
1231,10.1016/j.jcat.2010.09.027,sol_gel_ceramic_synthesis,"A series of Ce-M (M = Zr, Zn, Fe) mixed oxides, wi ... ercentage mol.% (CeO2, CeZr10, CeZn10 and CeFe10)."
1232,10.1007/s10800-012-0464-7,sol_gel_ceramic_synthesis,LiMn2O4 was prepared by sol-gel method. Stoichiome ... grinding as such was subjected to further studies.
1233,10.1016/j.elecom.2012.02.026,sol_gel_ceramic_synthesis,LiFe(MoO4)2 was synthesized by the Pechini sol-gel ... alcined at 600 degC for 6 h to obtain the product.
1234,10.1016/j.matchemphys.2007.04.038,sol_gel_ceramic_synthesis,CdFe2O4 nanopowder was prepared by sol-gel method. ... ly then calcined between 700 and 900 degC for 4 h.
1235,10.1016/j.solidstatesciences.2015.09.014,sol_gel_ceramic_synthesis,"The powder of gadolinium-doped ceria (Ce0.8Gd0.2O2 ... mixed, ground and calcined at 600 degC for 30 min."
1236,10.1016/j.jallcom.2013.03.281,sol_gel_ceramic_synthesis,The LiFePO4/C composites were prepared by a sol-ge ...  for another 10 h to obtain the LiFePO4/C powders.
1237,10.1002/aenm.201400107,sol_gel_ceramic_synthesis,"Synthesis of Carbon Decorated Li3V2(PO4)3: The mat ... tio of V2O5/H2C2O4 from 1:3 to 1:7), respectively."
1238,10.1016/j.jpowsour.2014.06.129,sol_gel_ceramic_synthesis,The powders of A-site deficient SFM perovskites in ... rs were then calcined at 1050 degC in air for 5 h.
1239,10.1016/j.matlet.2013.01.099,sol_gel_ceramic_synthesis,"The Bi1-xErxFe0.95Co0.05O3 (BEFCO) (x=0, 0.05, 0.1 ...  obtained powder was calcined at 550 degC for 2 h."
1240,10.1016/j.cattod.2010.11.097,sol_gel_ceramic_synthesis,Sr1-xKxTiO3 (x = 0.1-0.5) mixed oxides with perovs ... mposition was calcined in air at 850 degC for 6 h.
1241,10.1007/s10853-009-3631-4,sol_gel_ceramic_synthesis,Ce-Ti oxide samples were prepared by a sol-gel met ...  h at 600 degC to obtain Ce0.3Ti0.7O2 called CeTi.
1242,10.1016/j.matchemphys.2014.06.031,sol_gel_ceramic_synthesis,The CaMoO4:10mol%Yb3+ phosphors doped with Li+ ion ... t 700 degC for 4 h to obtain the phosphor samples.
1243,10.1016/j.jpowsour.2016.05.107,sol_gel_ceramic_synthesis,The sol-gel method was adopted to synthesize Li1.2 ... procedure using CoC2O4.2H2O as a cobalt precursor.
1244,10.1016/j.materresbull.2006.08.018,sol_gel_ceramic_synthesis,"The stoichiometric amounts of H3PO4, Fe(NO3)3, CH3 ...  prepared by the same sol-gel process without PEG."
1245,10.1016/j.matlet.2006.12.071,sol_gel_ceramic_synthesis,BaCo0.5Nb0.5O3 was prepared via a sol-gel method.  ... 500 degC for 30 min to form the precursor powders.
1246,10.1016/j.cattod.2007.03.036,sol_gel_ceramic_synthesis,"CeO2 was prepared by precipitation, Zr0.1Ce0.9O2,  ... d oven and calcined under air for 5 h at 500 degC."
1247,10.1016/j.jallcom.2015.05.013,sol_gel_ceramic_synthesis,The strontium substituted CFO ferrites with compos ... e calcined at the temperature of 800 degC for 3 h.
1248,10.1016/j.apsusc.2016.05.163,sol_gel_ceramic_synthesis,The Bi1-xCaxFe1-xTixO3 nanoparticles with x = 0.00 ... n well nanocrystalline Bi1-xCaxFe1-xTixO3 powders.
1249,10.1016/j.electacta.2010.12.075,sol_gel_ceramic_synthesis,The composite oxides of SSCx (0.2 <= x <= 0.8) and ... to obtain the product with the target composition.
1250,10.1016/j.jssc.2004.01.009,sol_gel_ceramic_synthesis,"RE2Ti2O7 samples (RE=Sm, Eu, Gd, Y) were prepared  ...  15 min and sintered at 1673 K in air for 10-30 h."
1251,10.1016/j.jcis.2015.01.031,sol_gel_ceramic_synthesis,"Fe/ZrO2 nanocatalyst was synthesized by a sol-gel  ... esignated as FZN, containing 8 wt.% of Fe content."
1252,10.1007/s10854-013-1295-y,sol_gel_ceramic_synthesis,"M-type strontium hexaferrite powders were prepared ... e dry gel was calcined at 1,000 degC for 1 h [26]."
1253,10.1016/j.electacta.2013.07.069,sol_gel_ceramic_synthesis,"The Li-rich layered oxide, Li1.2Mn0.54Ni0.13Co0.13 ...  degC for 12 h in air to obtain the final product."
1254,10.1007/s10854-013-1530-6,sol_gel_ceramic_synthesis,"Zn1-xNdxO, (x = 0.0, 0.03, 0.06 and 0.10) nanopart ... air ambience resulting in Zn1-xNdxO nanoparticles."
1255,10.1016/j.ijhydene.2010.03.039,sol_gel_ceramic_synthesis,BaZr0.4Ce0.4Y0.2O3-δ (BZCY4) electrolyte and Ba0.5 ... d at 1000 degC for 5 h to form the target powders.
1256,10.1016/j.molcata.2007.09.005,sol_gel_ceramic_synthesis,A series of catalysts were prepared by the sol-gel ... nd sieved to 20-40 meshes for the catalytic tests.
1257,10.1016/j.jmmm.2015.06.016,sol_gel_ceramic_synthesis,"The nanoparticles of Bi1-y-xBayErxFeO3 were synthe ... ly, the powders were annealed at 650 degC for 1 h."
1258,10.1016/j.ijhydene.2010.07.038,sol_gel_ceramic_synthesis,LSCM powders were prepared using a sol-gel combust ... esulting powder was calcined at 1000 degC for 5 h.
1259,10.1016/j.matlet.2013.08.061,sol_gel_ceramic_synthesis,BiFeO3 and Bi0.8La0.2FeO3 nanoparticles were synth ... d process was described in the previous Ref. [10].
1260,10.1016/j.jpowsour.2012.12.107,sol_gel_ceramic_synthesis,The cathode material Li(Li0.23Mn0.47Fe0.2Ni0.1)O2  ... re to obtain Li(Li0.23Mn0.47Fe0.2Ni0.1)O2 powders.
1261,10.1016/j.ijhydene.2014.04.106,sol_gel_ceramic_synthesis,The electrolyte BaCe0.7Zr0.15Y0.15O3-δ (BCZY) powd ...  SSC powders from Winner Technology Co. were used.
1262,10.1016/j.solidstatesciences.2013.02.008,sol_gel_ceramic_synthesis,"BFO and (1 - x)BFO-xNBT with x = 0.1, 0.2 and 0.3  ... calcined at 600 degC are denoted as 0.8BFO-0.2NBT."
1263,10.1016/j.jcat.2005.10.001,sol_gel_ceramic_synthesis,A series of Fe-Mn-Zn-Ti-O mixed-metal oxides were  ... t 500 degC for 4 h before storage and further use.
1264,10.1016/j.cattod.2013.11.055,sol_gel_ceramic_synthesis,All of the catalysts were prepared by a modified s ... y calcined at 1000 degC for 5 h under ambient air.
1265,10.1016/j.solidstatesciences.2013.05.001,sol_gel_ceramic_synthesis,"At the second stage, ZnFe2O4 nanoparticles were pr ... urnt at 900 degC to get the ZnFe2O4 nanoparticles."
1266,10.1007/s10854-015-3671-2,sol_gel_ceramic_synthesis,"Powders Bi1-xEuxFeO3 of (BEFO) with \( x = 0,{ 0}  ... samples were annealed at 500 degC in air for 24 h."
1267,10.1016/j.cplett.2012.01.047,sol_gel_ceramic_synthesis,Poly vinyl alcohol (PVA) assisted sol-gel method h ...  PVA and hence to obtain phase pure YCrO3 powders.
1268,10.1016/j.cattod.2011.03.080,sol_gel_ceramic_synthesis,LaNiO3 perovskite catalysts were prepared from the ... 0 degC for 6 h using a heating rate of 2 degC/min.
1269,10.1016/j.matlet.2017.01.082,sol_gel_ceramic_synthesis,LTO and LLTSO were synthesized by a modified sol-g ...  using 1-Methyl-2-pyrrolidone (NMP) as dispersant.
1270,10.1016/j.apcatb.2010.11.027,sol_gel_ceramic_synthesis,"Sr2Mg1-xMnxMoO6-δ (x = 0, 0.2, 0.5, 0.8 and 1) cat ... n for 12 h to form the expected crystalline phase."
1271,10.1007/s10008-008-0627-y,sol_gel_ceramic_synthesis,"Li4Mn5O12 was prepared by a sol-gel process with L ... 0, 600, and 700 degC for 4 h in air, respectively."
1272,10.1016/j.matchemphys.2005.01.039,sol_gel_ceramic_synthesis,Li1+yNi0.5AlxMn0.5-xO2 powders were synthesized us ...  and then cooled at 2 K min-1 to room temperature.
1273,10.1016/j.electacta.2004.04.033,sol_gel_ceramic_synthesis,Li[Li0.12NizMg0.32-zMn0.56]O2 with z = 0.28 and 0. ... nd then thoroughly ground using mortar and pestle.
1274,10.1016/j.jssc.2010.04.019,sol_gel_ceramic_synthesis,Polycrystalline samples of Nd0.3Sm0.7NiO3 were pre ... egC under 175 and 20 bar oxygen pressure for 12 h.
1275,10.1016/j.cattod.2014.06.042,sol_gel_ceramic_synthesis,The Ce0.5La0.5O2 - δ solid (Ce:La = 1:1 nominal at ... pare the Ce0.5La0.5O2 - δ-OA solid (M:OA = 1:1.5).
1276,10.1016/j.matchemphys.2011.04.007,sol_gel_ceramic_synthesis,"Porous LiNi1/3Co1/3Mn1/3O2 powders were synthesize ...  same sol-gel process, named as pristine material."
1277,10.1007/s10854-012-0733-6,sol_gel_ceramic_synthesis,The powder with a composition of 0.63BMT-0.37PT +  ...  0.63BMT-0.37PT was optimized at this temperature.
1278,10.1016/j.cej.2015.12.035,sol_gel_ceramic_synthesis,"La2NiMnO6 was prepared by a sol-gel method. La(NO3 ... e method, using KNO3 (AR) as the potassium source."
1279,10.1016/j.mssp.2013.12.024,sol_gel_ceramic_synthesis,"In the present study, TiO2 and the Cr-doped mixed  ... strength of the resulting powders became stronger."
1280,10.1016/j.jmmm.2013.08.057,sol_gel_ceramic_synthesis,Mn1-xZnxFe2O4 powders were synthesized by sol-gel  ... errite was confirmed by XRD using Cu-Kα radiation.
1281,10.1016/j.jeurceramsoc.2015.02.015,sol_gel_ceramic_synthesis,The key of sol-gel method was to prepare xBA-(1 -  ... 5 h. The detail process was illustrated in Fig. 1.
1282,10.1016/j.electacta.2016.06.069,sol_gel_ceramic_synthesis,"Firstly, micro-sized Li1.172Ni0.135Co0.135Mn0.539O ... desired micron Li-rich layered oxide was obtained."
1283,10.1002/ente.201500153,sol_gel_ceramic_synthesis,LaNiO3 powder was synthesized by a sol-gel combust ... and then ground for 5 h to form the LaNiO3 powder.
1284,10.1016/j.jmmm.2011.11.033,sol_gel_ceramic_synthesis,The nanoparticles of Bi0.8Ca0.2-xBaxFeO3 (BCBFOx)  ... preheated powders annealed at 650 degC for 30 min.
1285,10.1016/j.snb.2009.03.050,sol_gel_ceramic_synthesis,SiO2-Al2O3 (1/1) was used as the support. This sup ... anics. The support is denoted as SiO2-Al2O3 (1:1).
1286,10.1016/j.solidstatesciences.2012.01.030,sol_gel_ceramic_synthesis,"Solid solutions La1-xAxMnO3 (A = Sr, Ba) were synt ... ed following the procedure described in Ref. [15]."
1287,10.1016/j.electacta.2013.12.096,sol_gel_ceramic_synthesis,"Typically, the powder of LiMn2O4 was prepared by t ...  K in air for 10 h to get spinel LiMn2O4 products."
1288,10.1016/j.apcata.2010.02.012,sol_gel_ceramic_synthesis,"La2NiO4+δ (LN), La2Ni0.95V0.05O4.07+δ (LNV-05) and ... s size of 0.1-0.3 mm was used for all experiments."
1289,10.1016/j.snb.2016.10.018,sol_gel_ceramic_synthesis,Barium titanate was synthesised by using sol-gel m ... esis of barium titanate powder is shown as Fig. 2.
1290,10.1016/j.matchemphys.2011.02.027,sol_gel_ceramic_synthesis,Nanopowders of pure and Ti-doped LiMnPO4 were obta ... chemical performance of the LiMnPO4 cathodes [17].
1291,10.1016/j.snb.2004.11.063,sol_gel_ceramic_synthesis,An amorphous precursor of NASICON was prepared by  ... r 5 h to obtain the powder of crystalline NASICON.
1292,10.1016/j.jpowsour.2011.09.088,sol_gel_ceramic_synthesis,Trimetallic perovskites with formula Sm1-xCexFeO3+ ... ion and its composition was confirmed by XRF [30].
1293,10.1016/j.materresbull.2007.10.009,sol_gel_ceramic_synthesis,"Layer-structured cathode material LiNi0.375Co0.25M ... r 18 h, followed by quenching to room temperature."
1294,10.1016/j.electacta.2013.08.002,sol_gel_ceramic_synthesis,"A typical sol-gel process is performed as follows: ...  with nitrate and acetate for short, respectively."
1295,10.1007/s10854-015-2982-7,sol_gel_ceramic_synthesis,"In the present investigation, the samples with nom ... ir atmosphere for 4 h followed by furnace cooling."
1296,10.1016/j.jallcom.2009.06.027,sol_gel_ceramic_synthesis,"The orthotellurates of formula Ln2TeO6 (Ln = Y, La ... roducts showed homogeneous powders of white color."
1297,10.1016/j.ssi.2010.03.026,sol_gel_ceramic_synthesis,The cathode material Sm0.5Sr0.5CoO3 - δ (SSC) was  ... rin to get slurry with fine particle distribution.
1298,10.1016/j.jlumin.2012.11.012,sol_gel_ceramic_synthesis,"Herewith described, CaY2Al4SiO12:Ce3+ samples with ... red for 4 h at 1400-1450 degC under CO atmosphere."
1299,10.1016/j.jpowsour.2012.01.001,sol_gel_ceramic_synthesis,Series of Sm and Sr co-doped ceria powders with fo ... te the residence carbon and form well crystalline.
1300,10.1016/j.jpowsour.2013.10.137,sol_gel_ceramic_synthesis,"LTSO was synthesized by the sol-gel method using t ... TSO material, was also applied to LTO preparation."
1301,10.1016/j.mseb.2017.03.005,sol_gel_ceramic_synthesis,All chemical reagents were of analytical grade and ... e BFO or Sm-doped BFO nanoparticles were obtained.
1302,10.1016/j.jallcom.2015.04.166,sol_gel_ceramic_synthesis,"LiNi1/3Co1/3Mn1/3-xNbxO2 (x = 0, 0.01, 0.02, 0.03) ... degC for 10 h to get the LiNi1/3Co1/3Mn1/3-xNbxO2."
1303,10.1016/j.elecom.2007.05.012,sol_gel_ceramic_synthesis,Lithium samarium holmium silicate (LiSm0.25Ho0.75S ...  preparation of LiSm0.25Ho0.75SiO4 is given below:
1304,10.1016/j.jcrysgro.2008.09.185,sol_gel_ceramic_synthesis,"In this article, the SrTiO3 powder was made by sol ... Then SrTiO3 was grinded to powder in ball grinder."
1305,10.1016/j.jpowsour.2016.02.056,sol_gel_ceramic_synthesis,"For a comparison, ZnMnO4 microparticles were synth ...  at 600 degC for 10 h to obtain the final product."
1306,10.1016/j.jcis.2004.11.049,sol_gel_ceramic_synthesis,The Cu015Ce0.85O2-y oxide sample was prepared by a ... atalysts was checked by means of ICP-AES analysis.
1307,10.1016/j.jpowsour.2011.03.019,sol_gel_ceramic_synthesis,Ba1.0Sr1.0FeO4+δ (BSFO) powders were synthesized b ... egC for 8 h in air and BSFO powders were obtained.
1308,10.1016/j.apcatb.2015.04.019,sol_gel_ceramic_synthesis,"A series of Ce-Zr mixed oxides, with different Zr  ... ed by the same procedure for comparative purposes."
1309,10.1016/j.jpowsour.2012.07.058,sol_gel_ceramic_synthesis,Pristine LMNO was synthesized by sol-gel method as ...  as the pristine material for the following study.
1310,10.1016/j.nimb.2016.03.041,sol_gel_ceramic_synthesis,In this work copper substituted nickel ferrite Ni  ... or 2 h in the air to achieve single phase samples.
1311,10.1016/j.jallcom.2011.02.163,sol_gel_ceramic_synthesis,"Ni1-xZnxFe2O4 (x = 0, 0.25, 0.4, 0.5 and 0.6) were ... at 1200 degC for 12 h followed by furnace cooling."
1312,10.1007/s10800-012-0405-5,sol_gel_ceramic_synthesis,Nanoparticles of LiCoO2 were synthesized by a citr ... 0 degC for 10 h to obtain nanoparticles of LiCoO2.
1313,10.1016/j.jpcs.2011.06.006,sol_gel_ceramic_synthesis,"BiFe1-xNixO3 (with x=0, 0.1) nanoceramics were pre ... the sintered pellets are described elsewhere [13]."
1314,10.1016/j.cattod.2008.08.013,sol_gel_ceramic_synthesis,"All the samples were prepared by the sol-gel metho ... lution, Yili) and Ce(NO3)3*6H2O as the precursors."
1315,10.1016/j.materresbull.2015.10.029,sol_gel_ceramic_synthesis,Polycrystalline phosphors of Dy3+ (1.0 mol%) doped ... oichiometric reaction can be described as follows:
1316,10.1016/j.jallcom.2015.11.188,sol_gel_ceramic_synthesis,All nanoparticles having formula Co1-x Rex Fe2 O4  ... he synthesis of samples are illustrated in Fig. 1.
1317,10.1007/s10971-016-4150-9,sol_gel_ceramic_synthesis,LiNi0.5Mn1.5O4 material is microwave synthesized b ... d LiNi0.5Mn1.5O4 is subjected to characterization.
1318,10.1016/j.jpowsour.2011.07.020,sol_gel_ceramic_synthesis,"The BZCY7 powder was synthesized using citrate-nit ... , and the synthesized BZCY7 powders were obtained."
1319,10.1007/s10008-004-0532-y,sol_gel_ceramic_synthesis,A series of samples with nominal LiCuxMn2-xO4 (wit ... ed compounds with LiCu0.5-yMyMn1.5O4stoichiometry.
1320,10.1016/j.electacta.2004.03.055,sol_gel_ceramic_synthesis,"For the acetate self-mixing preparation of LiCoO2, ... ttent cooling and grinding procedures at 900 degC."
1321,10.1016/j.jssc.2015.10.017,sol_gel_ceramic_synthesis,"NaYP2O7 and NaYP2O7:Ln (Ln=Eu, Ce) polycrystalline ... perimental conditions used for sample preparation."
1322,10.1111/j.1751-1097.2011.01064.x,sol_gel_ceramic_synthesis,"Synthesis. Cerium-doped TiO2 nanoparticles, having ... lline product was cerium-doped TiO2 nanoparticles."
1323,10.1007/s10948-014-2480-9,sol_gel_ceramic_synthesis,The synthesis of Bi1-xDyxFeO3 nanoparticles was ca ... 0 degC (Dy 550) and 650 degC (Dy 650) for 4 hours.
1324,10.1016/j.ssi.2005.01.003,sol_gel_ceramic_synthesis,"The P2-Na2/3(Ni1/3-xMn2/3-xM2x)O2 (M=Cr, Co, x=0.0 ... , calcined at 850 degC for 10 h and then quenched."
1325,10.1016/j.jssc.2013.10.012,sol_gel_ceramic_synthesis,"The [Co(Ca1-xSrx)2O3]qCoO2 (x=0, 0.1, 0.2, 0.3 and ... t 900 degC for 24 h to reach decent crystallinity."
1326,10.1016/j.ijhydene.2015.09.148,sol_gel_ceramic_synthesis,SDC powder was synthesized by a sol-gel method. Fi ... egC for 4 h. The SDC powder was milled before use.
1327,10.1016/j.jpowsour.2016.06.084,sol_gel_ceramic_synthesis,LFMP/C composites coated with different amounts of ... es coated with different amounts (1-3 wt%) of LTO.
1328,10.1016/j.jeurceramsoc.2009.02.012,sol_gel_ceramic_synthesis,"Nb2O5 (99.9%), KOH (97%), Li2CO3 (97%), Na2CO3 (99 ... ls were precisely controlled from 400 to 650 degC."
1329,10.1016/j.materresbull.2010.09.021,sol_gel_ceramic_synthesis,"LiMn2O4 powder was prepared by the sol-gel method, ... n at 850 degC for 15 h to get pure LiMn2O4 powder."
1330,10.1016/j.electacta.2011.06.100,sol_gel_ceramic_synthesis,The citrate-based sol-gel method was adopted to pr ... cted to heat-treatment in air at 800 degC for 2 h.
1331,10.1016/j.matchemphys.2008.06.030,sol_gel_ceramic_synthesis,The sample with the general formula of Ce0.8Gd0.2- ... lar pellets were used for electrical measurements.
1332,10.1016/j.apcata.2009.12.023,sol_gel_ceramic_synthesis,"Liu et al. [67] prepared an N-Ce co-doped TiO2 via ...  air, and thereafter calcined at 500 degC for 2 h."
1333,10.1016/j.cplett.2014.07.057,sol_gel_ceramic_synthesis,BZO powder was synthesized using a standard comple ... sphere at 900 degC for 3 h to get crystalline BZO.
1334,10.1016/j.tsf.2007.06.025,sol_gel_ceramic_synthesis,The other type of the nano-TiO2 sample was fabrica ... C for 6 h to obtain particle powders for analysis.
1335,10.1016/j.optmat.2012.09.018,sol_gel_ceramic_synthesis,KGW particles were prepared using polymeric comple ... or various characterization studies [14] and [15].
1336,10.1007/s10008-004-0521-1,sol_gel_ceramic_synthesis,The general process of the sol-gel method is simil ...  above 400 degC to obtain crystalline LiNiO2 [26].
1337,10.1016/j.cattod.2015.09.018,sol_gel_ceramic_synthesis,TiO2 nanoparticles were prepared by the sol-gel me ...  sample of TiO2 nanoparticles was labeled as (NP).
1338,10.1016/j.mseb.2013.11.028,sol_gel_ceramic_synthesis,"Nanocrystals of SLA doped with Mn2+ ions (0.02 mol ... er, next annealed at 1450 degC in furnace for 4 h."
1339,10.1016/j.msec.2014.05.077,sol_gel_ceramic_synthesis,Fe/TiO2 was prepared by the sol-gel method. Briefl ... te of 2 degC min- 1) to produce Fe/TiO2 composite.
1340,10.1007/s10854-015-3982-3,sol_gel_ceramic_synthesis,The Er3+ doped YVO4 nano- phosphors are prepared b ... temperatures ranging from 300 to 900 degC for 3 h.
1341,10.1016/j.jssc.2010.04.014,sol_gel_ceramic_synthesis,"For synthesizing Cr-doped ZnO nanoparticles, Zn1-x ... rized for their structural and optical properties."
1342,10.1016/j.cattod.2007.12.069,sol_gel_ceramic_synthesis,"LaNi1-xCoxO3 ternary oxides were prepared by the r ... 0 degC and calcined at 750 degC (4 h, 3 degC/min)."
1343,10.1016/j.physb.2015.10.019,sol_gel_ceramic_synthesis,BFO and BCFO nanoparticles were synthesized by sol ... 80 degC for 48 h and calcined at 550 degC for 2 h.
1344,10.1016/j.jallcom.2010.03.053,sol_gel_ceramic_synthesis,The raw materials used in the present work were an ... f the gel was calcined at 700 degC for 2 h in air.
1345,10.1016/j.cattod.2013.10.062,sol_gel_ceramic_synthesis,The lanthanum and boron co-doped samples were prep ...  the absence of La(NO3)3 and H3BO3 for comparison.
1346,10.1016/j.jpowsour.2009.02.076,sol_gel_ceramic_synthesis,"A sol-gel route using iron powders as starting mat ... , 0.75, and 0.5 for the further XAS investigation."
1347,10.1007/s00339-013-8134-0,sol_gel_ceramic_synthesis,The TiO2-CeO2 nanocomposites were prepared via the ... . Hereby t50-c50 means 50 % of TiO2 and 50 % CeO2.
1348,10.1016/j.ijhydene.2010.05.058,sol_gel_ceramic_synthesis,Samples of SmBaCoFeO5+δ (SBCF) were prepared by a  ...  using the glycine-nitrate combustion method [21].
1349,10.1016/j.fuproc.2014.04.028,sol_gel_ceramic_synthesis,Copper-ferrite spinel was prepared by the sol-gel  ... esulting spinel was calcined at 900 degC for 10 h.
1350,10.1016/j.ssi.2011.11.019,sol_gel_ceramic_synthesis,LiFePO4 was prepared in a modified sol-gel process ... idue of the decomposition of the complexing agent.
1351,10.1016/j.cej.2010.06.006,sol_gel_ceramic_synthesis,LaNiO3 catalyst was prepared by sol-gel method. In ... catalyst was crushed and used as powder form [15].
1352,10.1016/j.jpowsour.2015.07.003,sol_gel_ceramic_synthesis,Sm0.2Ce0.8O1.9 (SDC) powders were prepared by a ty ... ld SDC powders with the desired lattice structure.
1353,10.1016/j.molcata.2009.09.022,sol_gel_ceramic_synthesis,"In the citric acid sol-gel method, the raw materia ... the obtained yellow powder CeO2 was denoted as CA."
1354,10.1007/s10853-015-9679-4,sol_gel_ceramic_synthesis,Polycrystalline delafossite oxides CuCr1-xZnxO2 (x ...  mortar and sintered in air at 1000 degC for 10 h.
1355,10.1016/j.optmat.2014.05.025,sol_gel_ceramic_synthesis,"Lu3Al5O12:Cr3+ and Lu3Al5O12:Ce3+,Cr3+ powder samp ... lour of Ce3+/Cr3+ doped samples were dirty yellow."
1356,10.1016/j.physb.2009.06.148,sol_gel_ceramic_synthesis,LiMn2O4 and LiMgxMn2-xO4 were prepared by sol-gel  ... ealed in the presence of air at 750 degC for 12 h.
1357,10.1016/j.matchemphys.2012.05.070,sol_gel_ceramic_synthesis,In order to prepare Zinc Aluminate nanoparticles b ...  powder. The resulting powders are denoted as ZAO.
1358,10.1007/s10854-016-4651-x,sol_gel_ceramic_synthesis,Ferrite particles were prepared by a simplified so ... mable furnace to produce the required cubic phase.
1359,10.1016/j.jallcom.2016.12.082,sol_gel_ceramic_synthesis,"Nanoparticles of Bi1-xBaxFe1-yCoyO3 with x = 0,y = ... rming pure and substituted BFO nanoparticles [21]."
1360,10.1007/s10854-016-4929-z,sol_gel_ceramic_synthesis,"The sol-gel method was used to synthesize LCTO pow ... 1110 and 1115 degC for 10, 15, 20 h, respectively."
1361,10.1016/j.fuel.2014.06.017,sol_gel_ceramic_synthesis,The sol-gel method is also used to synthesize CTF  ...  to become embedded in the CTF perovskite support.
1362,10.1016/j.solidstatesciences.2004.04.008,sol_gel_ceramic_synthesis,LaSrAlO4 was synthesised both by sol-gel and combu ...  in air for 12 h to obtain a single-phase product.
1363,10.1016/j.jpowsour.2009.07.056,sol_gel_ceramic_synthesis,"Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF), the cathode mater ... owder was then used for cathode layer preparation."
1364,10.1016/j.cej.2011.05.092,sol_gel_ceramic_synthesis,"In sol-gel method, tartaric acid was used as a com ...  to room temperature, and marked as NCMO-2 sample."
1365,10.1007/s10854-015-3213-y,sol_gel_ceramic_synthesis,The pure BaTiO3 powders were prepared through sol- ... e resistivity can be 10-3-10-4 Ω cm were obtained.
1366,10.1016/j.mssp.2006.01.074,sol_gel_ceramic_synthesis,"Zn1-x Nix O ( x = 0 , 0.01, 0.02 and 0.05) powders ... in, then annealed at 600 degC in nitrogen for 1 h."
1367,10.1016/j.cplett.2014.11.025,sol_gel_ceramic_synthesis,Na-substituted Li2-xNaxMnSiO4 (x = 0.1 and 0.2) wa ... dium acetate trihydrate as the substituting agent.
1368,10.1016/j.jpowsour.2013.04.014,sol_gel_ceramic_synthesis,"Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF), Sm0.5Sr0.5CoO3-δ  ... r 5 h in static air to yield the desired catalyst."
1369,10.1016/j.jallcom.2016.07.094,sol_gel_ceramic_synthesis,BFO nanoparticles were synthesized by metal ions c ... 50 degC to obtain well crystallized nanoparticles.
1370,10.1016/j.optmat.2012.03.001,sol_gel_ceramic_synthesis,The LLM:Eu phosphors with different Eu3+ doping co ... ocedure with the corresponding starting materials.
1371,10.1016/j.mseb.2013.03.005,sol_gel_ceramic_synthesis,"Sr(Al1.98, B0.02)O4:xEu2+ were prepared by the sol ... the synthesis of (Sr1-z, Caz) (Al1-y, By)2O4:Eu2+."
1372,10.1016/j.electacta.2013.07.005,sol_gel_ceramic_synthesis,Ce0.8Sm0.2O1.9 (SDC) powders were prepared by the  ... orm LSCF powders with a desired crystal structure.
1373,10.1016/j.optmat.2014.09.029,sol_gel_ceramic_synthesis,Cr-doped MgGa2O4 nanoparticles with the compositio ...  the desired temperatures (700-1000 degC) for 5 h.
1374,10.1016/j.cattod.2011.02.015,sol_gel_ceramic_synthesis,"A series of Ce-Zn mixed oxides (Zn content of 10,  ... eZnX where X accounts for the Zn molar percentage."
1375,10.1007/s10008-010-1103-z,sol_gel_ceramic_synthesis,All chemical reagents used in this study were anal ... were obtained by calcination at 850 degC for 18 h.
1376,10.1007/s10008-012-1764-x,sol_gel_ceramic_synthesis,The Na-doped Li3V2(PO4)3/C cathode materials were  ...  prepared in the same process without using NaNO3.
1377,10.1002/zaac.201400615,sol_gel_ceramic_synthesis,"Sample Preparation: The nanosized ceria-manganese  ... 0, CeMnO-20, CeMnO-30, and CeMnO-40, respectively."
1378,10.1016/j.jnoncrysol.2004.12.012,sol_gel_ceramic_synthesis,Monoclinic zirconia was purchased from Aldrich. Te ... nealing the amorphous samples at 700 degC for 2 h.
1379,10.1007/s10008-012-1952-8,sol_gel_ceramic_synthesis,"The syntheses of Mn1.5Co1.5O4 (MC), La0.8Sr0.2FeO3 ... nol for 5 h and finally dried at room temperature."
1380,10.1016/j.jpowsour.2015.02.019,sol_gel_ceramic_synthesis,0.5Li2MnO3*0.5LiNi0.5Co0.2Mn0.3O2 (LLMO) was synth ... heating the precursor at 900 degC for 12 h in air.
1381,10.1016/j.jssc.2006.10.003,sol_gel_ceramic_synthesis,Sol-gel method is suitable to prepare optical mate ... 700-900 degC for 1 h to get the CeO2:Er3+ powders.
1382,10.1016/j.jmmm.2014.12.085,sol_gel_ceramic_synthesis,All the chemicals and solvents were of analytical  ... eping all other experimental conditions unchanged.
1383,10.1016/j.jmmm.2012.04.059,sol_gel_ceramic_synthesis,The BaFe12O19/Ni0.8Zn0.2Fe2O4 nanocomposite ferrit ... 0 degC) for 2 h to form the nanocomposite ferrite.
1384,10.1016/j.ssi.2005.02.010,sol_gel_ceramic_synthesis,The Li4Ti5O12 powder was synthesized by the sol-ge ... egC for different times to obtained final powders.
1385,10.1016/j.jmmm.2015.09.062,sol_gel_ceramic_synthesis,"Bismuth ferrite nanoparticles (BiFeO3) have been p ... rately, at temperatures 450-650 degC for 2 h [22]."
1386,10.1016/j.mseb.2007.12.001,sol_gel_ceramic_synthesis,Phosphors with the nominal formula of ZnGa2-xO4:xE ... ate from the stoichiometric formula ZnGa2-xO4:xEu.
1387,10.1111/j.1551-2916.2011.04536.x,sol_gel_ceramic_synthesis,BiFeO3 sample was synthesis by a sol-gel process u ... egC for 2 h in static air to obtain BiFeO3 powder.
1388,10.1016/j.jmmm.2012.10.033,sol_gel_ceramic_synthesis,The preparation of nanocomposite has been done in  ...  annealed at 500 degC in argon atmosphere for 1 h.
1389,10.1016/j.memsci.2014.07.058,sol_gel_ceramic_synthesis,"The magnesium aluminate particles were prepared by ... l chemicals have been purchased from Aldrich, USA."
1390,10.1016/j.electacta.2006.10.063,sol_gel_ceramic_synthesis,LiNi0.5Mn1.5O4 powders were prepared by a sol-gel  ... for 15 h in air to get LiNi0.5Mn1.5O4 powders [6].
1391,10.1016/j.jallcom.2010.04.149,sol_gel_ceramic_synthesis,"All chemical reagents used in this study were A.R. ...  24 h were marked as A, B, C, and D, respectively."
1392,10.1016/j.apcata.2010.10.025,sol_gel_ceramic_synthesis,"The fluorite oxides Ni-CZ, Ni-Rh-CZ and Ni-Ru-CZ w ... degC for 6 h, with a heating ramp of 2 degC min-1."
1393,10.1016/j.ssi.2010.08.020,sol_gel_ceramic_synthesis,"The La2-xAxMo2O9-δ (A = Ca, Sr, Ba, and K) films w ... repeated to fabricate thicker films [40] and [41]."
1394,10.1016/j.jpcs.2007.03.014,sol_gel_ceramic_synthesis,"Gd 2 O 3 (99.99%), Eu 2 O 3 (99.99%), nitric acid  ... erature oven at the required temperatures for 2 h."
1395,10.1016/j.ijggc.2012.11.011,sol_gel_ceramic_synthesis,In order to investigate the effect of the sol-gel  ... alcined at 700 degC for 2 h in the muffle furnace.
1396,10.1016/j.jmmm.2016.05.035,sol_gel_ceramic_synthesis,"Co1-xSrxFe2O4 (x=0.00, 0.01, 0.015, 0.02, 0.05, 0. ...  reaction involved in the synthesis is as follows:"
1397,10.1016/j.snb.2014.06.073,sol_gel_ceramic_synthesis,"NASICON precursor was prepared from ZrO(NO3)2, NaN ... C for 3 h to form the ZnTiO3 compound metal oxide."
1398,10.1016/j.optmat.2015.08.027,sol_gel_ceramic_synthesis,Nano-crystalline ytterbium doped yttrium disilicat ...  12 h to produce nano-crystalline Y2Si2O7 powders.
1399,10.1016/j.electacta.2005.01.022,sol_gel_ceramic_synthesis,Commercially available cathode powder of LiNi0.8Co ... ed to 200 degC/h for all the temperature settings.
1400,10.1016/j.ssc.2007.10.021,sol_gel_ceramic_synthesis,SFMO samples were prepared by the sol-gel method;  ... ) in a stream of 5% H2 in a N2 atmosphere for 5 h.
1401,10.1016/j.jpowsour.2010.06.088,sol_gel_ceramic_synthesis,Lithium-ion conducting LLTO particles were prepare ... d then sieved through a #325 mesh for further use.
1402,10.1016/j.matlet.2011.08.005,sol_gel_ceramic_synthesis,The ZnFe2O4 nanoparticles and target material were ... d pellet was sintered in air at 900 degC for 10 h.
1403,10.1016/j.apcatb.2010.09.018,sol_gel_ceramic_synthesis,SrTiO3 and Sr0.8K0.2TiO3 with perovskite-like stru ... mposition was calcined in air at 850 degC for 6 h.
1404,10.1007/s10008-008-0531-5,sol_gel_ceramic_synthesis,The oxygen reduction perovskite catalyst La0.6Ca0. ... to fine powder and ground using mortar and pestle.
1405,10.1016/j.electacta.2014.05.108,sol_gel_ceramic_synthesis,The stoichiometric lithium manganese oxide LiMn2O4 ... mperature method (LTM) of LMO/1%wt.CeO2 synthesis.
1406,10.1016/j.apsusc.2012.09.177,sol_gel_ceramic_synthesis,High density polycrystalline target of La0.72Ca0.2 ... as further used as the target for preparing films.
1407,10.1016/j.physc.2006.10.005,sol_gel_ceramic_synthesis,Lightly doped La2-xSrxCuO4 (x = 0.04) nanoparticle ... annealed at 600 degC for 10 h in flowing nitrogen.
1408,10.1002/aenm.201400982,sol_gel_ceramic_synthesis,Materials Preparation: The precursors of the NVP-C ... as mentioned above except for the addition of PVP.
1409,10.1016/j.cej.2016.03.032,sol_gel_ceramic_synthesis,CeO2-TiO2 mixed oxides with various molar ratios o ... ly pressed and sieved to 40-60 meshes before used.
1410,10.1007/s10008-011-1544-z,sol_gel_ceramic_synthesis,F-doped LiFePO4/C was prepared with a sol-gel meth ... ng the same procedure without the addition of LiF.
1411,10.1007/s10854-015-2866-x,sol_gel_ceramic_synthesis,"Bi1-xTbxFeO3 (x = 0, 0.05) nanoparticles were synt ... ) and 650 degC (sample 5T6) for 4 h, respectively."
1412,10.1016/j.tsf.2011.10.166,sol_gel_ceramic_synthesis,"Samples of cerium oxide CeO2 were produced with th ...  thermally treated for 5 h at 500 degC, under air."
1413,10.1016/j.materresbull.2006.12.015,sol_gel_ceramic_synthesis,"All samples are prepared by sol-gel process: appro ... ing M2(Mg, Zn)Si2O7:Mn2+ (M = Ca, Sr, Ba) samples."
1414,10.1007/s10854-014-2107-8,sol_gel_ceramic_synthesis,ZnO powders with different Fe doping concentration ... 2 h and 700 degC for 4 h in succession in an oven.
1415,10.1016/j.matlet.2015.10.100,sol_gel_ceramic_synthesis,LTO composites were synthesized with a sol-gel met ...  muffle furnace at 900 degCfor 20 h to obtain LTO.
1416,10.1016/j.matchemphys.2005.06.014,sol_gel_ceramic_synthesis,"A sol-gel method was employed to prepare layered L ... 3 h in air, and then quenched to room temperature."
1417,10.1007/s10008-013-2301-2,sol_gel_ceramic_synthesis,Pristine and Sm- and La-substituted spinel LiSmxLa ... . The calcined powders were ground well for 3-4 h.
1418,10.1007/s10853-006-1429-1,sol_gel_ceramic_synthesis,"The powders with the nominal composition of (Na0.5 ...  at 600 degC for 1 h, the powders can be obtained."
1419,10.1111/ijac.12244,sol_gel_ceramic_synthesis,YIG particles have been prepared using the citric  ... gC for 3 h to obtain crystalline particles of YIG.
1420,10.1016/j.jeurceramsoc.2011.03.015,sol_gel_ceramic_synthesis,The NiO-YSZ nanoparticles were obtained by a modif ... f obtaining the nanopowder is presented in Fig. 1.
1421,10.1007/s10854-013-1369-x,sol_gel_ceramic_synthesis,"In the present investigation, Zn0.98-xMn0.02CuxO ( ... ir atmosphere for 4 h followed by furnace cooling."
1422,10.1016/j.jpowsour.2014.09.183,sol_gel_ceramic_synthesis,"La0.7Sr0.3Mn0.7Co0.3O3-coated LiMn2O4 samples were ... , and the bare LiMn2O4 was designated as sample-0."
1423,10.1016/j.apcatb.2013.05.036,sol_gel_ceramic_synthesis,A series of nanometric perovskite catalysts La1-xK ...  flow to form spongeous powder of final catalysts.
1424,10.1007/s00339-014-8618-6,sol_gel_ceramic_synthesis,"La0.67Ca0.33MnO3 green body was synthesized by a s ... ed between 600 and 1,500 degC in the air for 12 h."
1425,10.1016/j.jallcom.2009.06.033,sol_gel_ceramic_synthesis,Fine particles of Cobalt ferrite were synthesized  ...  and sintered samples are designated as CP and C8.
1426,10.1016/j.physe.2016.03.032,sol_gel_ceramic_synthesis,To synthesize the MgO nanocrystallites by aqueous  ... o obtain samples of the desired crystallite sizes.
1427,10.1016/j.jpowsour.2007.01.063,sol_gel_ceramic_synthesis,The Dy-doped NiO powder was prepared from metallic ... ant products were reduced to about 1-mm particles.
1428,10.1007/s10854-016-5772-y,sol_gel_ceramic_synthesis,Sample of hexagonal magnetoplumbite type ferrite B ... in to the final elevated temperature in a furnace.
1429,10.1016/j.jpowsour.2011.12.047,sol_gel_ceramic_synthesis,The LVP/C composite material was synthesized by a  ...  atmosphere to yield the LVP/C composite material.
1430,10.1016/j.optmat.2014.03.018,sol_gel_ceramic_synthesis,The nanocrystals were prepared in the Institute of ... lcined in the air atmosphere at 1000 degC for 7 h.
1431,10.1016/j.electacta.2013.06.075,sol_gel_ceramic_synthesis,"The materials discussed in this paper were synthes ...  Sn/Fe ratio of 1:99, 3:97 and 5:95, respectively."
1432,10.1016/j.electacta.2015.06.085,sol_gel_ceramic_synthesis,The pristine Li1.18Co0.15Ni0.15Mn0.52O2 was prepar ... for 12 h followed by quenching in liquid nitrogen.
1433,10.1016/j.jpowsour.2004.12.006,sol_gel_ceramic_synthesis,The sol-gel process was adapted to the synthesis o ... 00 degC for 8 h in air to obtain the spinel phase.
1434,10.1016/j.apcatb.2004.09.015,sol_gel_ceramic_synthesis,Al2O3-La2O3 binary oxides with varying concentrati ... wed by calcination in an oven at 650 degC for 4 h.
1435,10.1016/j.cattod.2007.10.036,sol_gel_ceramic_synthesis,Nanocrystalline α-Al2O3 and Ni-modified α-Al2O3 we ... n followed the same procedures as that of α-Al2O3.
1436,10.1016/j.electacta.2012.12.054,sol_gel_ceramic_synthesis,"Li9V3-xMnx(P2O7)3(PO4)2 (x = 0.00, 0.02, 0.05, 0.0 ... ered at 750 degC under the same ambience for 10 h."
1437,10.1016/j.optmat.2010.11.023,sol_gel_ceramic_synthesis,Y3-xLuxAl3MgSiO12 samples were synthesized by an a ... intering at 1600 degC for 4 h under CO atmosphere.
1438,10.1016/j.fuel.2015.01.061,sol_gel_ceramic_synthesis,"TiO2, CeO2/TiO2 and CeO2-WO3/TiO2 catalysts were p ...  percentage of CeO2 and WO3 to TiO2, respectively."
1439,10.1016/j.electacta.2013.07.026,sol_gel_ceramic_synthesis,MgFe2O4 nanoparticles were synthesized by a sol-ge ... ed at 500 degC for 2 h in the muffle furnace [22].
1440,10.1016/j.electacta.2014.12.119,sol_gel_ceramic_synthesis,"Analytical pure NH4VO3, lithium oxalate, sodium ox ... n a motor and annealed at 400 degC for 4 h in air."
1441,10.1016/j.jelechem.2007.08.004,sol_gel_ceramic_synthesis,Powdered CuCo2O4 was synthesized using a sol-gel m ... 3 h under air atmosphere to form the oxide powder.
1442,10.1016/j.matchemphys.2007.04.004,sol_gel_ceramic_synthesis,"Cr-doped LiMn2-xCrxO4 [x = 0.1, 0.2, 0.3 and 0.4]  ... ric acid through sol-gel route as given in Fig. 1."
1443,10.1016/j.mseb.2011.01.003,sol_gel_ceramic_synthesis,The (Y1-xEux)2O3 particles were prepared by a Pech ...  materials and to obtain the nanophosphor powders.
1444,10.1016/j.matchemphys.2006.11.016,sol_gel_ceramic_synthesis,Gadolinium aluminate (GdAlO3) ceramic samples were ... nthesis of the GdAlO3 ceramics is shown in Fig. 1.
1445,10.1007/s10854-011-0549-9,sol_gel_ceramic_synthesis,The BT powder was prepared by a solid state reacti ... a heating rate of 5 degC/min to get the BF powder.
1446,10.1016/j.matlet.2010.03.023,sol_gel_ceramic_synthesis,The C12A7-O- particles were prepared by the citric ...  and finally formed the powder sample of C12A7-O-.
1447,10.1016/j.electacta.2013.10.215,sol_gel_ceramic_synthesis,Li[Li0.18Ni0.15Co0.15Mn0.52]O2 was synthesized by  ... 00 degC in air for 12 h and quenched in liquid N2.
1448,10.1016/j.matchemphys.2005.12.035,sol_gel_ceramic_synthesis,"LiNi0.8-xCo0.2CexO2 compounds, where x = 0.00, 0.0 ... ooled and ground to a fine polycrystalline powder."
1449,10.1007/s00339-016-0207-4,sol_gel_ceramic_synthesis,"PbTi1-xFexO3 nanoparticles with x = 0.00, 0.02, 0. ... temperatures for 3 h to crystallize the materials."
1450,10.1016/j.jpowsour.2014.04.096,sol_gel_ceramic_synthesis,Perovskite oxide nanoparticles were synthesized by ... 0 degC for 2 h to obtain perovskite oxide powders.
1451,10.1016/j.electacta.2016.02.210,sol_gel_ceramic_synthesis,"Dual doped Li1.2-xNaxMn0.6-xAlxNi0.2O2 (x = 0, 0.0 ... named as D0, D1, D2, D3, D4, and D5, respectively."
1452,10.1016/j.ssi.2012.01.013,sol_gel_ceramic_synthesis,Phosphosilicate gel powders were prepared via a so ... wders were then dried at 140 degC for 24 h in air.
1453,10.1016/j.cej.2011.01.079,sol_gel_ceramic_synthesis,The Er3+ (1.0%):YAlO3 as up-conversion luminescenc ...  ions and finally form the Er3+:YAlO3 nanocrystal.
1454,10.1016/j.cattod.2009.12.010,sol_gel_ceramic_synthesis,Sol-gel catalysts were synthesized by a pseudo sol ... epared via a sol-gel route are referred to as CZS.
1455,10.1016/j.apcata.2007.07.005,sol_gel_ceramic_synthesis,The nanoparticle catalysts were prepared by a sol- ...  the precursors were calcined at 300 degC for 3 h.
1456,10.1007/s10008-012-1851-z,sol_gel_ceramic_synthesis,"In sol-gel method, a precursor mix consisting of a ...  ground and subjected to characterization studies."
1457,10.1016/j.jallcom.2013.07.007,sol_gel_ceramic_synthesis,Macroporous LiNi0.5Co0.2Mn0.3O2 powders were synth ... btain the macroporous LiNi0.5Co0.2Mn0.3O2 powders.
1458,10.1016/j.jpowsour.2016.02.066,sol_gel_ceramic_synthesis,Six samples with the nominal stoichiometry Na3V2-x ... ing an Elemental CHNS Eurovector EA 3000 analyzer.
1459,10.1007/s10854-015-4029-5,sol_gel_ceramic_synthesis,BiFeO3 nanoparticles were synthesized by the citri ...  in air at 600 degC in tubular resistance furnace.
1460,10.1016/j.matchemphys.2012.10.019,sol_gel_ceramic_synthesis,"In the aqueous sol-gel process, the following mate ... ere further sintered in air at 1000 degC for 10 h."
1461,10.1007/s10854-014-2132-7,sol_gel_ceramic_synthesis,The pure and Yb (1 and 3 %) doped SrTiO3 compounds ... 0 degC for 4 h to achieve high crystalline nature.
1462,10.1016/j.jpcs.2006.09.012,sol_gel_ceramic_synthesis,Pb1-xCaxTiO3 (x=0-0.35%) powders have been prepare ... ts by using polyvinyl alcohol (PVA) as the binder.
1463,10.1016/j.apcatb.2007.09.039,sol_gel_ceramic_synthesis,"The catalyst was prepared by sol-gel method. All c ... n to Ti, respectively, e.g., Fe(0.1)-Mn(0.4)/TiO2."
1464,10.1007/s10854-015-3223-9,sol_gel_ceramic_synthesis,"The polycrystalline samples of pure and Cr (5, 10, ... 0 degC for 4 h to achieve high crystalline nature."
1465,10.1016/j.jpowsour.2005.05.065,sol_gel_ceramic_synthesis,"Fine Zr-incorporated LiCoO2 (hereafter called Zr-L ... r:Co molar ratios of 0.97 and 0.015, respectively."
1466,10.1016/j.matchemphys.2013.03.023,sol_gel_ceramic_synthesis,"Compared with the solid-state method, the reaction ...  for 5 h to obtain the requisite phosphor samples."
1467,10.1016/j.ijhydene.2011.11.122,sol_gel_ceramic_synthesis,LSM oxide powder was synthesized by a combined eth ... t the products with the desired lattice structure.
1468,10.1016/j.mseb.2007.07.056,sol_gel_ceramic_synthesis,TiO2:Pr was first prepared by sol-gel process usin ...  room temperature to obtain doped TiO2 nanopowder.
1469,10.1016/j.jpcs.2015.07.006,sol_gel_ceramic_synthesis,The SrFe12O19 powder was obtained using the sol-ge ... h at 250 degC under an oxygen flow of 200 cm3/min.
1470,10.1016/j.matchemphys.2009.12.014,sol_gel_ceramic_synthesis,"The RE (Eu3+, Sm3+ and Eu3+/Dy3+) doped yttrium va ... hen ground and used for further preparation steps."
1471,10.1016/j.jpowsour.2015.06.146,sol_gel_ceramic_synthesis,"Li3-xNaxV2-xTix(PO4)3/C (x = 0, 0.01, 0.03, 0.05,  ... re heated at 650 degC for 3 h in an Ar atmosphere."
1472,10.1007/bf02838527,sol_gel_ceramic_synthesis,Normal spinel LiMn2O4 was synthesized by sol-gel m ... MnO2 can be obtained after lithium ion extraction.
1473,10.1016/j.electacta.2013.05.151,sol_gel_ceramic_synthesis,"W-doped and pure lithium titanates, Li4Ti5-xWxO12  ... of Li during the high temperature heating process."
1474,10.1016/j.optmat.2011.02.017,sol_gel_ceramic_synthesis,"The Ce3+ and Tb3+ co-doped Ln2Si2O7 (Ln = Y, Gd) s ... epared samples appeared to be white color in body."
1475,10.1016/j.electacta.2014.04.155,sol_gel_ceramic_synthesis,"LiCoO2 cathode material was synthesized by a sol-g ... perature, finally yielding black powder of LiCoO2."
1476,10.1002/jctb.4578,sol_gel_ceramic_synthesis,"CaFe2O4 nanoparticles were synthesized by a sol-ge ...  calcined at 673 K, 973 K and 1173 K for 8 h each."
1477,10.1007/s10854-014-2163-0,sol_gel_ceramic_synthesis,"Zr doped BFO (BiFe1-xZrxO3, x = 0.03, 0.07, 0.10 a ... in order to obtain crystallized BFO nanoparticles."
1478,10.1002/ep.11688,sol_gel_ceramic_synthesis,The Er0.03Y2.97Al5O12 samples were prepared by the ... les were obtained after cooling in air atmosphere.
1479,10.1016/j.actamat.2008.06.004,sol_gel_ceramic_synthesis,"LnBaCo2O5+δ (Ln = La,Y, Pr, Nd, Sm and Gd) composi ... sphere to yield the desired oxide powder products."
1480,10.1016/j.electacta.2014.04.178,sol_gel_ceramic_synthesis,The other Li3V2(PO4)3/C composite was prepared by  ... egC in Ar atmosphere to obtain the LVP/C-2 sample.
1481,10.1016/j.jmatprotec.2007.06.061,sol_gel_ceramic_synthesis,"The powder samples were prepared by the sol-gel me ...  700 and 1000 degC) for 3 h (Zhao and Zhou, 2004)."
1482,10.1016/j.jeurceramsoc.2016.06.017,sol_gel_ceramic_synthesis,Ni-Zn ferrite with a chemical formula of Ni0.5Zn0. ... egC for 1 h and Ni-Zn ferrite powder was obtained.
1483,10.1016/j.ijhydene.2007.07.034,sol_gel_ceramic_synthesis,Preparation of thin films by sol-gel : In the sol- ... The thin films were sintered at 500 [?] C for 2 h.
1484,10.1016/j.ssi.2013.12.006,sol_gel_ceramic_synthesis,LLZ was prepared by a sol-gel process using LiNO3  ... emperatures between 600 degC and 900 degC for 5 h.
1485,10.1007/s10853-006-0099-3,sol_gel_ceramic_synthesis,"CoxNi1-xFe2O4 (0.0 <= x <= 1.0) ferrite powders we ... 2 h, yielding the materials examined in this work."
1486,10.1016/j.cplett.2016.01.005,sol_gel_ceramic_synthesis,For the synthesis of NiSb2O6 sol-gel method was ad ...  be described by the following chemical reactions:
1487,10.1016/j.jpowsour.2008.12.005,sol_gel_ceramic_synthesis,"The fine powders of Y0.7Ca0.3Cr1-xZnO3-δ (x = 0, 0 ... on and to obtain the highly reactive fine powders."
1488,10.1016/j.snb.2015.01.043,sol_gel_ceramic_synthesis,The Ni3V2O8 was prepared from nickel nitrate (Ni(N ... ffle furnace by a gradual increase of temperature.
1489,10.1007/s00339-014-8795-3,sol_gel_ceramic_synthesis,Polycrystalline samples of La1-xCexAl2B3O9 (x = 0. ... ded with the active carbon to reduce to Ce3+ ions.
1490,10.1016/j.electacta.2015.03.138,sol_gel_ceramic_synthesis,The Li2Zn0.6Cu0.4Ti3O8 was prepared by a typical s ... under the same condition without adding Cu-source.
1491,10.1016/j.ijhydene.2016.01.024,sol_gel_ceramic_synthesis,"AFe2O4 spinel ferrite catalysts (A = Ni, Co, Mn, M ... esis procedure have been previously described [4]."
1492,10.1016/j.cattod.2015.05.009,sol_gel_ceramic_synthesis,"Mg(NO3)2 (>99.9%, Strem), Ga(NO3)3*6H2O (>99.9%, S ...  under atmospheric pressure in a proper fume hood."
1493,10.1016/j.jallcom.2009.09.165,sol_gel_ceramic_synthesis,Carbon coated LiFePO4 composite materials were pre ... rement procedure can be found in the article [27].
1494,10.1016/j.ssi.2015.11.011,sol_gel_ceramic_synthesis,PBCNO powders were prepared by a combined EDTA-cit ... of SDC and NiO power with a weight ratio of 35:65.
1495,10.1007/s10854-015-3411-7,sol_gel_ceramic_synthesis,"Nickel nitrate Ni(NO3)2, copper nitrate Cu(NO3)2,  ... composites during 8.2-12.4 GHz were characterized."
1496,10.1016/j.materresbull.2015.11.050,sol_gel_ceramic_synthesis,Li4Ti5O12/anatase-TiO2 nanocomposites were prepare ... timum temperature of synthesis for nanocomposites.
1497,10.1002/celc.201500164,sol_gel_ceramic_synthesis,Layered-spinel integrated composite materials with ...  were collected after cooling to room temperature.
1498,10.1016/j.apsusc.2014.03.087,sol_gel_ceramic_synthesis,"In this synthesis, LaMnO3 were prepared via sol-ge ...  degC for 2 h to obtain pure LaMnO3 nanoparticles."
1499,10.1016/j.jlumin.2011.06.015,sol_gel_ceramic_synthesis,"Ca3Ga2(1-x)Si3O12:RE2x3+ (RE=Sm, Dy and x=1, 5, 10 ... duced in the host powder phosphors are as follows:"
1500,10.1007/s10800-013-0627-1,sol_gel_ceramic_synthesis,Three different LVP samples were prepared via a so ... id and oxalic acid will be indicated as LVP/CA+OA.
1501,10.1016/j.matchemphys.2012.05.011,sol_gel_ceramic_synthesis,The Y-Al-M-O or Y-Fe-Co-O precursor gels were prep ... substituted garnet samples is presented in Fig. 1.
1502,10.1007/s00339-014-8258-x,sol_gel_ceramic_synthesis,"Based on Ref. [7], the optimum concentration for T ... 0 degC for 2 h in air to obtain the final samples."
1503,10.1016/j.apsusc.2005.08.002,sol_gel_ceramic_synthesis,Catalysts were prepared using a modified sol-gel m ... o-precipitation method and calcinated at 400 degC.
1504,10.1016/j.electacta.2013.07.121,sol_gel_ceramic_synthesis,The Ni-doped TiO2 powder was prepared by a sol-gel ... used in the experiments were in analytical purity.
1505,10.1016/j.jssc.2006.06.029,sol_gel_ceramic_synthesis,The Bi2Fe4O9 precursors in this work were prepared ...  Then it was increased to 1073 K and kept for 3 h.
1506,10.1016/j.electacta.2016.02.065,sol_gel_ceramic_synthesis,Bare Li[Li0.2Ni0.17Co0.07Mn0.56]O2 was synthesized ... egC in air for 12 h to obtain the target material.
1507,10.1016/j.jelechem.2009.11.035,sol_gel_ceramic_synthesis,Li2Fe0.97Mg0.03SiO4 was prepared by a sol-gel meth ... en calcined at 700 degC for 12 h in flowing argon.
1508,10.1016/j.jpcs.2008.09.021,sol_gel_ceramic_synthesis,The samples of LiMn1.4Cr0.2Ni0.4O4 spinel were pre ...  product at a cooling rate of 5 degC min-1 in air.
1509,10.1016/j.jallcom.2011.05.083,sol_gel_ceramic_synthesis,The (1 - x)BiFeO3-xBi0.5Na0.5TiO3 (x = 0.37) (BF-B ... sed into pellets and sintered at 950 degC for 3 h.
1510,10.1016/j.matchemphys.2011.04.020,sol_gel_ceramic_synthesis,SnO2 nanowires were synthesized by a sol-gel metho ... recursor of Sn-C-O composite powders was obtained.
1511,10.1016/j.cattod.2014.06.010,sol_gel_ceramic_synthesis,"A sol-gel method was applied to prepare the mixed- ... r 4 h. After calcination, the catalyst was tested."
1512,10.1016/j.apcata.2010.06.024,sol_gel_ceramic_synthesis,"PrBaCo2O5+δ (PBC), Ba0.5Sr0.5Co0.8Fe0.2O3-δ (BSCF) ... he relative low calcination temperatures employed."
1513,10.1016/j.optmat.2003.11.006,sol_gel_ceramic_synthesis,The polycrystalline Ce3+ doped yttrium oxyorthosil ... ue to the rather high final annealing temperature.
1514,10.1007/s10800-009-9911-5,sol_gel_ceramic_synthesis,The Li4Mn5O12 particles were synthesized by a sol- ... d at 500 degC for 8 h to obtain the final product.
1515,10.1007/s10853-014-8737-7,sol_gel_ceramic_synthesis,The starting materials were standard reagents and  ... e annealed at 1173 K for 36 h under O2 atmosphere.
1516,10.1016/j.matchemphys.2015.12.043,sol_gel_ceramic_synthesis,The Y-Al-M-O (M = In or Cr) precursor gels were pr ... dditionally sintered for 10 h at 1000 degC in air.
1517,10.1016/j.electacta.2006.06.024,sol_gel_ceramic_synthesis,Li[Li0.07Ni0.1Co0.6Mn0.23]O2 materials were prepar ... 10 h at 950 degC and quenched to room temperature.
1518,10.1016/j.scriptamat.2015.08.008,sol_gel_ceramic_synthesis,"Y0.08Sr0.92Ti1 - xScxO3 - δ (x = 0.03, 0.05, 0.07) ... ment of total electrical and ionic conductivities."
1519,10.1016/j.mseb.2006.09.007,sol_gel_ceramic_synthesis,Homogeneous magnetic-nonmagnetic composites of (1  ... ets and finally sintered at 1073 K in air for 2 h.
1520,10.1016/j.matlet.2005.10.060,sol_gel_ceramic_synthesis,"La0.8Na0.2MnO3 bulk samples were synthesized by so ...  degC, 1150 degC, 1200 degC for 5 h, respectively."
1521,10.1016/j.physb.2009.08.033,sol_gel_ceramic_synthesis,"Nano-polycrystalline powder of LKCMO were prepared ... us temperatures (i.e., 1000 [?] C ) for 10 h [16]."
1522,10.1016/j.optmat.2013.11.031,sol_gel_ceramic_synthesis,"In the present investigation, Zn0.96-xMn0.04CoxO ( ... ir atmosphere for 4 h followed by furnace cooling."
1523,10.1016/j.jpowsour.2016.06.134,sol_gel_ceramic_synthesis,Ln0.5Sr0*5Fe0*8Cu0*2O3-δ was synthesized where Ln  ...  ratio of 1:1 and firing them at 900 degC for 4 h.
1524,10.1016/j.synthmet.2011.08.022,sol_gel_ceramic_synthesis,The LVP/MWCNTsx composite cathode materials were p ... thesized samples could be obtained after grinding.
1525,10.1016/j.ssc.2008.08.018,sol_gel_ceramic_synthesis,"The Bi1-xCexFeO3 films with x = 0 , 0.05 and 0.10  ... ted several times to obtain the desired thickness."
1526,10.1016/j.mseb.2008.01.002,sol_gel_ceramic_synthesis,The (1 - x) La0.67Ca0.33MnO3/xCuFe2O4 samples (x = ... sed into pellets and sintered at 850 degC for 1 h.
1527,10.1016/j.fuel.2007.10.029,sol_gel_ceramic_synthesis,The CeO2-TiO2 binary oxides were prepared from Ce( ...  symbolized as CeO2-TiO2 (x:(10-x)) (molar ratio).
1528,10.1016/j.matchemphys.2012.04.017,sol_gel_ceramic_synthesis,The powder with a composition of 0.63BMT-0.37PT wa ...  in air in the temperature range of 990-1100 degC.
1529,10.1002/pc.22701,sol_gel_ceramic_synthesis,Barium hexaferrite powders were synthesized throug ... tered at 1000degC for 5 h in ash oven in air [15].
1530,10.1016/j.matchemphys.2013.12.038,sol_gel_ceramic_synthesis,"Y0.9Eu0.1V1-xCrxO4 samples (x = 0, 0.1, 0.2 and 0. ...  to dark green by increasing the chromium content."
1531,10.1016/j.jpcs.2009.05.005,sol_gel_ceramic_synthesis,Bulk polycrystalline samples with compositional fo ...  and finally sintered in air at 1200 degC for 4 h.
1532,10.1016/j.cattod.2014.11.032,sol_gel_ceramic_synthesis,"Ba-Mn based perovskite-type oxides were synthesize ... 800, BaMn900, BaMn1150 and BaMn800+, respectively."
1533,10.1016/j.electacta.2013.09.105,sol_gel_ceramic_synthesis,The pristine LiCoO2 powders are prepared by sol-ge ... ve at 700 degC for 10 h to produce LiCoO2 powders.
1534,10.1007/s10832-013-9802-3,sol_gel_ceramic_synthesis,The BaTiO3 powder was synthesized by sol-gel metho ... and the following grinding gave the BaTiO3 powder.
1535,10.1016/j.matchemphys.2012.01.104,sol_gel_ceramic_synthesis,"To synthesize Sm2FeTaO7 using sol-gel processing,  ... r atmosphere using a heating rate of 1 degC min-1."
1536,10.1016/j.optmat.2011.02.019,sol_gel_ceramic_synthesis,"Nanocrystalline ZrO2 doped with 0.5 mol.% of Er3+, ... or 2 h and finally cooled to the room temperature."
1537,10.1016/j.pmatsci.2011.08.002,sol_gel_ceramic_synthesis,If the salts are mixed with a hydrocarboxylic acid ... ed by calcining the dried gel at 800 degC for 5 h.
1538,10.1016/j.actamat.2013.08.060,sol_gel_ceramic_synthesis,"CaIn2-x-yHoxYbyO4 (x = 0.001, 0.003, 0.005, 0.007, ... arting materials of CaCO3, In2O3, Ho2O3 and Yb2O3."
1539,10.1016/j.ssc.2005.04.014,sol_gel_ceramic_synthesis,The microstructure of ceramic materials in general ... lets and were sintered at 900 degC in air for 4 h.
1540,10.1016/j.apcatb.2003.09.005,sol_gel_ceramic_synthesis,Metal oxide-doped Co/Al2O3 catalysts were prepared ...  were calcined finally at 600 degC for 4 h in air.
1541,10.1016/j.ijhydene.2010.12.113,sol_gel_ceramic_synthesis,PSCFSx (x = 0.0-0.2) were synthesized via an EDTA- ... e sol-gel method and calcined at 600 degC for 5 h.
1542,10.1016/j.mseb.2016.05.019,sol_gel_ceramic_synthesis,"MgFe1-xInxO4 nanoparticles (where x = 0.00, 0.04,  ... niques and explored for their magnetic properties."
1543,10.1016/j.electacta.2012.06.073,sol_gel_ceramic_synthesis,LnBaFe2O5+δ powders were synthesized via a combine ... sequently calcinated at 1000 degC for 10 h in air.
1544,10.1016/j.jmmm.2010.08.007,sol_gel_ceramic_synthesis,"In our experiments, polycrystalline manganite samp ... C for 48 h in air to obtain the ceramic compounds."
1545,10.1016/j.jpowsour.2011.11.051,sol_gel_ceramic_synthesis,The Li3V2(PO4)3/C cathode materials were prepared  ... e gas flow of high pure N2 to yield Li3V2(PO4)3/C.
1546,10.1016/j.cej.2010.04.034,sol_gel_ceramic_synthesis,The preparation of chromium (Cr) doped TiO2 and Cr ...  was similar to that of Cr doped TiO2 preparation.
1547,10.1016/j.jhazmat.2005.09.010,sol_gel_ceramic_synthesis,"Nanophase TiO2 catalysts were produced using a pro ... owder diffractometer (D8 advance, Bruker, German)."
1548,10.1016/j.jallcom.2013.01.026,sol_gel_ceramic_synthesis,BiFeO3 and BiFe0.95Co0.05O3 ceramics were prepared ... epeatedly to remove the trace amounts of impurity.
1549,10.1111/j.1551-2916.2009.02938.x,sol_gel_ceramic_synthesis,"The samples of Ce6-xGdxMoO15-δ were prepared by a  ...  the nitrates, followed by combustion of organics."
1550,10.1016/j.ssi.2011.11.024,sol_gel_ceramic_synthesis,"(Ba0.5Sr0.5)1 - xGdxCo0.8Fe0.2O3 - δ (x = 0, 0.02, ...  selected for the electrical conductivity testing."
1551,10.1016/j.mseb.2004.08.012,sol_gel_ceramic_synthesis,A LiMn2O4 powder was prepared by an aqueous sol-ge ... d by X-ray diffraction (XRD) analysis (see below).
1552,10.1016/j.jpowsour.2005.03.236,sol_gel_ceramic_synthesis,The TiO2-coated Ni powder was prepared by a sol-ge ...  organic substrate and all decomposable materials.
1553,10.1016/j.apcatb.2011.12.010,sol_gel_ceramic_synthesis,Nanostructured Ce-Al-O mixed oxides with different ... C for 4 h for decomposition of organic precursors.
1554,10.1016/j.jssc.2003.09.020,sol_gel_ceramic_synthesis,"Then, samples of xNdO1.5-(1-x)CeO2-δ (0x0.30) were ... gel was then thermally treated at 320degC for 2 h."
1555,10.1016/j.jpowsour.2004.11.031,sol_gel_ceramic_synthesis,The (Co/Mg)-coated Ni powder was prepared from a C ... C for 3 h to obtain the (Co/Mg)-coated Ni powders.
1556,10.1007/s10854-007-9527-7,sol_gel_ceramic_synthesis,The precursor solutions for undoped and doped BST  ... kness measured by an ellipsometer is about 300 nm.
1557,10.1016/j.electacta.2007.01.019,sol_gel_ceramic_synthesis,Li3V2(PO4)3/carbon composite material was synthesi ... hen sintered at 750 degC for 4 h in flowing argon.
1558,10.1016/j.nanoso.2016.08.001,sol_gel_ceramic_synthesis,A modified Pechini method and the metal complex me ... acid with EG ) and S 4 (phthalic acid without EG).
1559,10.1016/j.matchemphys.2008.05.013,sol_gel_ceramic_synthesis,LiV3O8 were synthesized by two methods. One is nor ...  the precursor at different temperatures for 10 h.
1560,10.1016/j.fuel.2011.03.009,sol_gel_ceramic_synthesis,"Besides coal samples, the Fe2O3 OC used (including ... o (as seen in Section 2.2) in a laboratory mortar."
1561,10.1016/j.jssc.2013.08.006,sol_gel_ceramic_synthesis,"Powder samples of composition LiMn1.5M0.5O4 (M=Fe, ... m 450 degC to 700 degC for a few hours in the air."
1562,10.1016/j.jpowsour.2014.08.068,sol_gel_ceramic_synthesis,LaNiO3 was synthesized by the citrate-based sol-ge ...  and mortar the black powder (LaNiO3) was crushed.
1563,10.1016/j.apsusc.2014.03.035,sol_gel_ceramic_synthesis,All of the reactants were of analytical grade and  ...  of 5 degC/min to obtain the ZnWO4/CNTs composite.
1564,10.1016/j.cattod.2004.04.059,sol_gel_ceramic_synthesis,"Electrolyte powder was synthesized by sol-gel meth ... 3 K for 4 h, and then ground again to fine powder."
1565,10.1016/j.jpowsour.2006.12.069,sol_gel_ceramic_synthesis,Li1.05Ni0.35Co0.25Mn0.4O2 (calcined at 1000 degC f ... in LiCoO2 coated Li1.05Ni0.35Co0.25Mn0.4O2 powder.
1566,10.1016/j.matchemphys.2015.12.002,sol_gel_ceramic_synthesis,Bismuth-Titanium Oxide nanopowders with different  ... hydroxilate and to produce a crystalline material.
1567,10.1016/j.matlet.2015.08.147,sol_gel_ceramic_synthesis,The YIG precursor sol was prepared by the sol-gel  ... lization. The cooling process was made to 25 degC.
1568,10.1016/j.electacta.2014.09.040,sol_gel_ceramic_synthesis,The nanosized pristine Li3V2(PO4)3 (abbreviated as ... min in flowing N2 by using microwave tube furnace.
1569,10.1016/j.jpowsour.2013.10.091,sol_gel_ceramic_synthesis,NaVPO4F was prepared by a sol-gel method [20]. V2O ... tube furnace at 800 degC for 6 h under flowing N2.
1570,10.1016/j.apcatb.2014.07.022,sol_gel_ceramic_synthesis,The MnFe2O4-SiC (or diatomite) powders were synthe ...  diatomite) in MnFe2O4-SiC (or diatomite) was 50%.
1571,10.1007/s10854-012-0622-z,sol_gel_ceramic_synthesis,"Zn1-xCuxO nanoparticles with x = 0.03, 0.05, 0.07  ...  the carrying gas to form Zn1-xCuxO nanoparticles."
1572,10.1016/j.matlet.2005.12.086,sol_gel_ceramic_synthesis,"For comparison purposes, conventional barium hexaf ... and finally thermally treated at 900 degC for 2 h."
1573,10.1016/j.ssi.2013.09.012,sol_gel_ceramic_synthesis,"Samples with nominal stoichiometry Li1.2 + xTi1.9  ... atmosphere, by applying a heat ramp of 3 degC/min."
1574,10.1016/j.optmat.2014.05.019,sol_gel_ceramic_synthesis,(4-x)MgO*xMgF2*GeO2:0.02Mn4+ samples were prepared ... ed samples were cooled slowly to room temperature.
1575,10.1007/s10853-013-7445-z,sol_gel_ceramic_synthesis,The polyacrylamide sol-gel process used to prepare ... ature (600-1200 degC) to obtain different samples.
1576,10.1016/j.jpowsour.2015.02.049,sol_gel_ceramic_synthesis,"The spinel LiMn1.94MO4 (M = Mn0.06, Mg0.06, Si0.06 ...  compounds were synthesized by the same technique."
1577,10.1016/j.jelechem.2014.02.013,sol_gel_ceramic_synthesis,All the samples were prepared by a sol-gel method. ... hen calcined at 700 degC for 8 h in flowing argon.
1578,10.1016/j.nanoen.2015.01.004,sol_gel_ceramic_synthesis,Bi0.5(Na0.82K0.18)0.5TiO3 (BNKT) and K0.5Na0.5Nb0. ... . Then the products were calcined at 650-800 degC.
1579,10.1111/j.1551-2916.2010.03640.x,sol_gel_ceramic_synthesis,"The Eu3+-doped BaLn2ZnO5 (Ln=Y, Gd, and La) phosph ... 0degC, for 5 h in air with 4degC/min heating rate."
1580,10.1016/j.jpowsour.2007.06.203,sol_gel_ceramic_synthesis,LiMnPO4 powder was prepared by a sol-gel method us ... mental temperatures (450-800 degC) for 3 h in air.
1581,10.1016/j.apsusc.2009.04.193,sol_gel_ceramic_synthesis,All the samples were prepared using a sol-gel meth ...  600 degC for 1 h to obtain Sn1-xMnxO2 thin films.
1582,10.1016/j.jpowsour.2013.02.019,sol_gel_ceramic_synthesis,Two different LVP samples were prepared via a sol- ...  and oxalic acid will be indicated as LVP/CA + OA.
1583,10.1016/j.physe.2012.09.019,sol_gel_ceramic_synthesis,"The Zn(NO3)2*6H2O (99.9%), NH4VO3 (99.9%), Cu(NO3) ...  were obtained after sol-gel process and sintered."
1584,10.1016/j.elecom.2008.06.021,sol_gel_ceramic_synthesis,Modified sol-gel method was used to synthesize nan ... tive atmosphere (named as MSG-Mg1.03Mn0.97SiO4/C).
1585,10.1016/j.jpcs.2007.01.009,sol_gel_ceramic_synthesis,The La1-xMgxFeO3 powders were prepared by sol-gel  ... fraction (XRD) to determine the phase composition.
1586,10.1016/j.optmat.2015.11.029,sol_gel_ceramic_synthesis,"The Gd1-xY(MoO4)3:xRE3+ (RE = Eu, Dy, Sm, Tb) samp ...  degC for 4 h in air to produce the final product."
1587,10.1002/pssb.201100561,sol_gel_ceramic_synthesis,The experimental procedure was carried out in two  ... at 600 degC for 4 h by using a ramp of 5 degC/min.
1588,10.1016/j.apcata.2009.09.005,sol_gel_ceramic_synthesis,"The fluorite oxides Ni-Ce0.72Zr0.28O2 were synthes ... degC for 6 h, with a heating ramp of 2 degC min-1."
1589,10.1016/j.snb.2013.04.096,sol_gel_ceramic_synthesis,"NASICON was synthesized from ZrO(NO3)2, NaNO3, (NH ... tes were 10 degC/min and 5 degC/min, respectively."
1590,10.1016/j.matchemphys.2010.12.045,sol_gel_ceramic_synthesis,Series of the perovskite-type La0.7Sr0.3Cr0.4Mn0.6 ... 12 h and then calcined at 800 degC for 1 h in air.
1591,10.1007/s10854-014-2635-2,sol_gel_ceramic_synthesis,The Bi2/3Cu3Ti4O12 (BCTO) samples were prepared by ... 0 degC for 7.5 h with a ramp rate of 2 degC min-1.
1592,10.1016/j.matchemphys.2004.09.031,sol_gel_ceramic_synthesis,"The synthesis procedures in the sol-gel process em ... nceforth named as S-T-14 and C-T-12, respectively."
1593,10.1016/j.mseb.2006.01.008,sol_gel_ceramic_synthesis,"The NFPs were prepared by the sol-gel method. Firs ... n bodies, absolutely following the sol-gel method."
1594,10.1016/j.optmat.2013.04.008,sol_gel_ceramic_synthesis,Eu3+-doped Ba3Y2WO9 phosphors were prepared by sol ... 0 degC for 10 h in air producing the white powder.
1595,10.1016/j.ssi.2010.08.019,sol_gel_ceramic_synthesis,The surface of the LiMn2O4 particles was modified  ...  the particles were heated at 350 degC for 30 min.
1596,10.1016/j.jpowsour.2011.08.114,sol_gel_ceramic_synthesis,"Li4Ti5O12 was synthesized based on a sol-gel metho ... , the color of the solution remained light yellow."
1597,10.1016/j.jpowsour.2014.03.013,sol_gel_ceramic_synthesis,The BZCY electrolyte powders were synthesized thro ... 0 degC in air for 5 h to obtain a BZCY perovskite.
1598,10.1016/j.electacta.2011.02.093,sol_gel_ceramic_synthesis,Li9V3-xCrx(P2O7)3(PO4)2 (x = 0.0-0.5) cathode mate ... ered at 750 degC for 10 h under the same ambience.
1599,10.1016/j.apcatb.2010.02.006,sol_gel_ceramic_synthesis,The MnOx-CeO2 mixed oxide catalyst was prepared by ... s CeO2 and MnOx were prepared by a similar method.
1600,10.1016/j.optmat.2011.11.011,sol_gel_ceramic_synthesis,The nanopowders were prepared using sol-gel method ... lcined in the air atmosphere at 1000 degC for 7 h.
1601,10.1016/j.cej.2014.01.017,sol_gel_ceramic_synthesis,"Calcium nitrate tetrahydrate (Ca(NO3)2*4H2O), yttr ... sents the weight percentage of CaO in the sorbent."
1602,10.1016/j.ssi.2015.11.028,sol_gel_ceramic_synthesis,Bare Li[Li0.2Ni0.17Co0.07Mn0.56]O2 was synthesized ... egC in air for 12 h to obtain the target material.
1603,10.1016/j.jpowsour.2016.06.065,sol_gel_ceramic_synthesis,Bulk CuCo2O4 were synthesized through a sol-gel me ... egC for 3 h in air to get the bulk CuCo2O4 powder.
1604,10.1016/j.matchemphys.2015.09.018,sol_gel_ceramic_synthesis,The 1-5 wt.% LTO-coated LFP/C composites were synt ... re to obtain 1-5 wt.% LTO-coated LFP/C composites.
1605,10.1016/j.jlumin.2011.05.060,sol_gel_ceramic_synthesis,For samarium-doped Sr4Al14O25 samples two differen ... 1400 degC) under CO or H2(10%)/N2(90%) atmosphere.
1606,10.1016/j.optmat.2010.04.031,sol_gel_ceramic_synthesis,"Y3-xMg2AlSi2O12: Ce x 3 + samples with different C ... guaranteed 100% CO atmosphere, irrespective of N2."
1607,10.1016/j.solidstatesciences.2010.07.015,sol_gel_ceramic_synthesis,"Zhou et al. [16] reported NiTiO3 powders by coprec ... ium isopropoxide, citric acid and ethylene glycol."
1608,10.1016/j.ssi.2005.08.015,sol_gel_ceramic_synthesis,Li[Co1-2x(Li1 / 3Mn2 / 3)x(Ni1 / 2Mn1 / 2)x]O2 (x  ... ts of Rietveld refinements from their XRD spectra.
1609,10.1016/j.electacta.2014.11.121,sol_gel_ceramic_synthesis,The Li3VO4 anode materials were synthesized via fa ... or 12 h under air atmosphere to yield pure Li3VO4.
1610,10.1016/j.electacta.2012.10.044,sol_gel_ceramic_synthesis,The Li2ZnTi3O8/C nanocomposite was prepared by usi ... ized by using the same route under air atmosphere.
1611,10.1016/j.jnoncrysol.2010.09.036,sol_gel_ceramic_synthesis,The precursor powders were synthesized by the sol- ... C for 3 hours in order to obtain a better SC path.
1612,10.1016/j.jallcom.2011.12.079,sol_gel_ceramic_synthesis,LiCoO2-coated LiMn2O4 was synthesized by a sol-gel ... iMn2O4 microspheres would be obtained as a result.
1613,10.1016/j.ijhydene.2012.06.102,sol_gel_ceramic_synthesis,The GdBaCo2O5+δ oxide powder was synthesized by a  ... terpineol binder to prepare the GBCO and SDC inks.
1614,10.1016/j.jpowsour.2006.07.019,sol_gel_ceramic_synthesis,The samples of spinel LiAl0.05Mn1.95O4 were prepar ... n air for 10 h to obtain the final spinel product.
1615,10.1016/j.powtec.2015.03.022,sol_gel_ceramic_synthesis,Zn0.6 - xNixCu0.4Fe2O4 (0 <= x <= 0.6) samples wer ... s process of our samples is represented in Fig. 1.
1616,10.1016/j.jeurceramsoc.2014.08.032,sol_gel_ceramic_synthesis,"Nanocrystalline La2Zr2O7 powders of single prochlo ... W*m-1*K-1, which was much lower than that of 7YSZ."
1617,10.1016/j.jpcs.2008.01.021,sol_gel_ceramic_synthesis,Red emitting phosphor samples R2-xEux(MoO4)3 (R=La ... ared by solid-state method according to Ref. [17].
1618,10.1016/j.jpcs.2010.10.074,sol_gel_ceramic_synthesis,The La0.875Ba0.125FeO3 nanocrystalline powders wer ... fraction (XRD) to determine the phase composition.
1619,10.1002/anie.200903444,sol_gel_ceramic_synthesis,Metal nitrates and citric acid (C6H8O7[?]H2O) were ... gel autocombustion in a tube furnace was 300 degC.
1620,10.1016/j.apsusc.2012.07.072,sol_gel_ceramic_synthesis,The BaFe12O19/Ni0.8Zn0.2 Fe2O4 nanocomposite ferri ... 00 degC for 2 h to form the nanocomposite ferrite.
1621,10.1007/s10853-011-5378-y,sol_gel_ceramic_synthesis,"TiO2 nanoparticles, with zinc and/or phosphorus do ... res, ranging 400-1,000 degC for 2 h, respectively."
1622,10.1007/s10854-014-1836-z,sol_gel_ceramic_synthesis,"In the present investigation, Zn0.96-xCo0.04CuxO ( ... ir atmosphere for 4 h followed by furnace cooling."
1623,10.1016/j.jallcom.2015.05.107,sol_gel_ceramic_synthesis,The raw materials were aluminum nitrate (Al(NO3)3[ ... taining MgAl2O4 spinel by modified sol-gel method.
1624,10.1016/j.jpcs.2013.02.005,sol_gel_ceramic_synthesis,"Ni0.5-2xMgxCu0.05Zn0.45+xFe2O4 (x=0.0, 0.04, 0.08, ... te of 2 degC/min in a programmable muffle furnace."
1625,10.1016/j.ijhydene.2014.08.131,sol_gel_ceramic_synthesis,Nd0.5Sr0.5Fe0.8Cu0.2O3-δ powders were synthesized  ... ed by Mastersizer 2000 (Malvern Instruments Ltd.).
1626,10.1016/j.jallcom.2012.02.112,sol_gel_ceramic_synthesis,Ca3-xMxCo4-yCuyO9 powders with different doping an ... PS process was described in our earlier work [12].
1627,10.1016/j.optmat.2013.04.028,sol_gel_ceramic_synthesis,"Besides, a powder SrLaAlO4:Mn(0.02%) was synthesiz ... onfirm the single phase compound of SLA structure."
1628,10.1016/j.synthmet.2014.07.027,sol_gel_ceramic_synthesis,The BaFe12O19/Ni0.8Zn0.2Fe2O4 nanocomposite ferrit ... 00 degC for 2 h to form the nanocomposite ferrite.
1629,10.1016/j.cattod.2004.09.012,sol_gel_ceramic_synthesis,BaTi1 - xNixO3 perovskite catalysts were prepared  ... r another 3 h to obtain three different catalysts.
1630,10.1016/j.matlet.2013.02.064,sol_gel_ceramic_synthesis,"The ZnO NPs have been synthesized using sol-gel me ... ir at 250, 500, 750, 1000 and 1250 degC, for 10 h."
1631,10.1016/j.matchemphys.2008.06.051,sol_gel_ceramic_synthesis,"The powders of Sr- and Mg-doped lanthanum gallate  ...  and Petric [4] and Tas et al. [16], respectively."
1632,10.1002/cssc.201500028,sol_gel_ceramic_synthesis,"BSCF, Sm0.5Sr0.5CoO3-δ (SSC), SDC powder was synth ... er catalytic activity and coking resistance tests."
1633,10.1016/j.msea.2006.10.011,sol_gel_ceramic_synthesis,Chemical processing techniques have been used to s ... l2O6 by combustion of metal nitrate-urea mixtures.
1634,10.1007/s10854-013-1543-1,sol_gel_ceramic_synthesis,"In the present investigation, Zn0.94Mn0.02Ni0.04O  ... on/diluted citric acid into the original solution."
1635,10.1016/j.apcatb.2012.09.015,sol_gel_ceramic_synthesis,"CuFe2O4 MNPs were prepared by sol-gel combustion m ... ctively, but with calcination at 400 degC for 1 h."
1636,10.1007/s10008-012-1810-8,sol_gel_ceramic_synthesis,"The LiNiyMnyCo1 - 2yO2 [y = 0.5, 0.45, and 0.4] ac ...  ground and subjected to characterization studies."
1637,10.1016/j.jpowsour.2013.07.114,sol_gel_ceramic_synthesis,LiNi0.5Mn1.5O4 powders were prepared via spray pyr ... treating the precursor in air at 800 degC for 4 h.
1638,10.1016/j.matchemphys.2005.06.029,sol_gel_ceramic_synthesis,"All chemicals were of analytical grade and were us ... h, followed by cooling to room temperature slowly."
1639,10.1007/s10008-014-2486-z,sol_gel_ceramic_synthesis,The cathode compound was synthesized by a sol-gel  ... r powder was calcined in air at 850 degC for 24 h.
1640,10.1016/j.optmat.2013.12.015,sol_gel_ceramic_synthesis,ZnO nanoparticles were prepared through sol-gel me ...  /min to obtain MgxZn1-xO with different x values.
1641,10.1016/j.fuel.2015.12.009,sol_gel_ceramic_synthesis,The four catalyst samples used in this study were  ... lycol was used as the solvent of antimony nitrate.
1642,10.1016/j.actamat.2008.10.047,sol_gel_ceramic_synthesis,LSSM oxide powder was synthesized by a combined ED ... final products with the desired lattice structure.
1643,10.1016/j.materresbull.2015.09.024,sol_gel_ceramic_synthesis,"All the chemicals used were analytical grade reage ... epared at Co/Bi molar ratio of 0.05, respectively."
1644,10.1016/j.jallcom.2006.06.007,sol_gel_ceramic_synthesis,"In order to obtain high purity and homogenous powd ...  pressing into pellets, this process was repeated."
1645,10.1016/j.ssi.2007.10.013,sol_gel_ceramic_synthesis,The (La0.9Sr0.1) (Cr0.85 Fe0.05 Co0.05 Ni0.05)O3 - ... nt of commonly observed SrCrO4 impurity phase [9].
1646,10.1016/j.jpowsour.2007.07.055,sol_gel_ceramic_synthesis,Spinel oxides with nominal stoichiometries CoFe2O4 ...  from 600 to 1000 degC for 24 h in air atmosphere.
1647,10.1016/j.ssi.2014.02.018,sol_gel_ceramic_synthesis,A series of Co-doped Li9V3 - xCox(P2O7)3(PO4)2/C ( ...  h under the same ambience in quartz tube furnace.
1648,10.1007/s10853-014-8033-6,sol_gel_ceramic_synthesis,MgxNi1-xFe2O4 powders with nominal compositions x  ... the sintered ceramics are in the range of 90-95 %.
1649,10.1016/j.jpowsour.2007.12.115,sol_gel_ceramic_synthesis,The citric acid assisted sol-gel method [14] has b ... eating rate of 5 degC per min at 800 degC for 8 h.
1650,10.1016/j.cattod.2011.03.002,sol_gel_ceramic_synthesis,CuOx-CeO2 mixed oxides were prepared through a cit ... xides. CeO2 was prepared through a similar method.
1651,10.1016/j.electacta.2010.07.059,sol_gel_ceramic_synthesis,"Li2Fe1-xCrxSiO4 (x = 0, 0.03, 0.06, 0.12) were pre ... en calcined at 700 degC for 12 h in flowing argon."
1652,10.1016/j.jallcom.2015.04.183,sol_gel_ceramic_synthesis,ZrO2 nanostructures of various sizes have been syn ... or studying its photocatalytic activity on MB dye.
1653,10.1016/j.matchemphys.2010.10.051,sol_gel_ceramic_synthesis,KNd2Ti3O9.5 was fabricated by stearic acid sol-gel ...  ranging from 400 degC to 900 degC for 2 h in air.
1654,10.1016/j.mseb.2005.11.042,sol_gel_ceramic_synthesis,The LiCo1-yNiyO2 (0.2 <= y <= 0.8) powders were sy ... ne grained materials of submicron-sized particles.
1655,10.1007/s10854-013-1596-1,sol_gel_ceramic_synthesis,Polycrystalline samples having the general formula ... d at a pressure of 8 ton cm-2 to form the pellets.
1656,10.1016/j.jpowsour.2008.04.087,sol_gel_ceramic_synthesis,Lanthanum aluminum garnet ceramic powders were syn ... o yield crystalline 3LaAlO3:Al2O3 ceramic powders.
1657,10.1016/j.mseb.2013.03.016,sol_gel_ceramic_synthesis,Chromium doped TiO2 nanoparticles with chromium co ...  h to get crystalline Cr doped TiO2 nanoparticles.
1658,10.1016/j.optmat.2012.01.034,sol_gel_ceramic_synthesis,Herewith described CaLu2Al4SiO12:Ce3+ samples with ... red for 4 h at 1400-1500 degC under CO atmosphere.
1659,10.1016/j.jeurceramsoc.2007.08.006,sol_gel_ceramic_synthesis,"For commonly hydrothermal treatment, a gel similar ... ed after calcination at about 1300 degC for 6 h.14"
1660,10.1016/j.jpcs.2015.12.015,sol_gel_ceramic_synthesis,The LLTO has been synthesized by sol-gel method [1 ... her fired at 900 degC for 1 h in a muffle furnace.
1661,10.1016/j.matlet.2012.04.118,sol_gel_ceramic_synthesis,The synthesis of SDC nanopowders through RF sol-ge ... eparation method and calcined at 500 degC for 3 h.
1662,10.1016/j.electacta.2008.02.002,sol_gel_ceramic_synthesis,Powdered MnxCu1-xCo2O4 samples with nominal compos ... form the oxide powders with different Mn contents.
1663,10.1016/j.jallcom.2010.08.146,sol_gel_ceramic_synthesis,"Analytical grade chromium nitrate [Cr(NO3)3*9H2O], ...  to about 773 K to remove out the binder material."
1664,10.1016/j.jpowsour.2013.01.135,sol_gel_ceramic_synthesis,Li4Ti5O12 was synthesized by the sol-gel method us ...  degC for different times to obtain final powders.
1665,10.1016/j.jpcs.2006.04.001,sol_gel_ceramic_synthesis,"The various samples of Sr, Mg-doped lanthanum gall ... iffraction and scanning electron microscopy (SEM)."
1666,10.1016/j.electacta.2003.11.001,sol_gel_ceramic_synthesis,"LiNi0.8-yTiyCo0.2O2 (y=0, 0.025, 0.050, 0.075, 0.1 ... eaction products were ground and filtrated lastly."
1667,10.1016/j.jallcom.2010.06.205,sol_gel_ceramic_synthesis,The W-type barium ferrite (Ba0.9Gd0.1(Zn0.3Co0.7)2 ... e the gel during the preparation of dry precursor.
1668,10.1016/j.cej.2012.07.010,sol_gel_ceramic_synthesis,The support and catalyst were prepared according t ... gC for 6 h to obtain the support CuO-Ce0.5Mn0.5O2.
1669,10.1016/j.jphotochem.2014.07.024,sol_gel_ceramic_synthesis,"The Ni-TiO2 photocatalysts were prepared with the  ...  as Ni1-TiO2, Ni2-TiO2 and Ni3-TiO2, respectively."
1670,10.1007/s10853-013-7538-8,sol_gel_ceramic_synthesis,SHA powder was synthesized by the sol-gel method r ... lcined at 600 degC for 5 h to obtain a SHA powder.
1671,10.1016/j.apsusc.2017.04.045,sol_gel_ceramic_synthesis,"Cu-TiO2 nanoparticles were synthesized by a sol-ge ... rocedures, and ZnAc was used as the ZnO precursor."
1672,10.1016/j.jcat.2015.06.009,sol_gel_ceramic_synthesis,"The sol-gel method: Cerium nitrate (Sigma-Aldrich, ... repared nanocomposite catalyst was named M1-Ce-SM."
1673,10.1016/j.cej.2014.12.035,sol_gel_ceramic_synthesis,The LaNiO3 NPs were prepared by the modified sol-g ... aled at 973 K for 3 h in air to obtain LaNiO3 NPs.
1674,10.1016/j.matlet.2016.06.118,sol_gel_ceramic_synthesis,"Powders Bi1-xEuxFeO3 of (BEFO) with x = 0 , 0.05 , ... n annealing treatment at 500 degC in air for 24 h."
1675,10.1016/j.ijhydene.2011.08.111,sol_gel_ceramic_synthesis,Nanocrystalline MYC powder was synthesized by a so ... owder was reduced in hydrogen at 700 degC for 2 h.
1676,10.1016/j.fuproc.2013.11.008,sol_gel_ceramic_synthesis,"The impregnation method employed here was based on ... Imp-Ti0.1, Imp-Ti0.2, and Imp-Ti0.3, respectively."
1677,10.1016/j.optmat.2015.05.019,sol_gel_ceramic_synthesis,"Y2.97(Al1-xGaX)5O12:Eu0.03 nanopowders were produc ... nto the initial solution, followed by evaporation."
1678,10.1016/j.materresbull.2004.08.013,sol_gel_ceramic_synthesis,"LiCrxMn2 - xO4 (x = 0.01, 0.02, 0.05, 0.10, 0.20)  ... ical as well as electrochemical characterizations."
1679,10.1016/j.cattod.2007.03.009,sol_gel_ceramic_synthesis,CexTi1-xO2 (x = 0.1-0.3) oxide samples were prepar ... r for 4 h at 600 degC to obtain CexTi1-xO2 oxides.
1680,10.1016/j.electacta.2012.02.076,sol_gel_ceramic_synthesis,"The sol-gel method was adopted to synthesize Li1.2 ... AA were named samples A, B, C and D, respectively."
1681,10.1016/j.cplett.2013.04.046,sol_gel_ceramic_synthesis,Undoped and Gd-doped BiFeO3 nanoparticles (Bi1-xGd ... ly washed with distilled water dried and grounded.
1682,10.1016/j.optmat.2004.10.020,sol_gel_ceramic_synthesis,The nanocrystalline YAG (NCYAG) samples were prepa ... was increased to 1150 degC and kept there for 4 h.
1683,10.1016/j.jpowsour.2014.09.143,sol_gel_ceramic_synthesis,The SSC powder was synthesized by a combined EDTA- ...  800 degC for 5 h in air to obtain the SDC powder.
1684,10.1016/j.electacta.2016.01.180,sol_gel_ceramic_synthesis,Pure lithium titanates were prepared by a sol-gel  ... ate for the volatilization of Li during synthesis.
1685,10.1016/j.jpowsour.2014.08.015,sol_gel_ceramic_synthesis,The procedure used for the synthesis of LMNO was a ...  another 24 h and was let to cool at 5 degC min-1.
1686,10.1007/s10854-014-1845-y,sol_gel_ceramic_synthesis,"The sol-gel method was used to synthesize ceramic  ... 0 and 1,100 degC for 5, 10 and 15 h, respectively."
1687,10.1016/j.apcatb.2012.02.003,sol_gel_ceramic_synthesis,W-TiO2 photocatalysts were prepared by the surface ... nt (80 degC) and calcinations at 400 degC for 1 h.
1688,10.1016/j.jpowsour.2005.05.033,sol_gel_ceramic_synthesis,"The samples were prepared using a standard sol-gel ...  LiMn0.6Fe0.4PO4), or 900 degC (LiMnPO4) for 10 h."
1689,10.1016/j.jlumin.2005.12.054,sol_gel_ceramic_synthesis,LiNbO3 and LiNbO3:Eu3+ nanocrystalline powders wer ... res for growing nanocrystals with different sizes.
1690,10.1016/j.jpowsour.2012.02.053,sol_gel_ceramic_synthesis,Pristine LiNi0.5Mn1.5O4 and W-doped LiWxNi0.5Mn1.5 ... es as the W content was varied from 0.005 to 0.10.
1691,10.1016/j.materresbull.2011.05.020,sol_gel_ceramic_synthesis,"Starting materials Lu2O3 (99.99%), Eu2O3 (99.99%), ... nd finally calcinated at 1100 degC for 4 h in air."
1692,10.1016/j.mseb.2012.04.023,sol_gel_ceramic_synthesis,For the synthesis of BaFe12O19 (barium hexaferrite ...  several times and dried at 100 degC in a furnace.
1693,10.1016/j.matlet.2005.07.012,sol_gel_ceramic_synthesis,All the chemical reagents used in the experiments  ... for 6 h. (This is the traditional sol-gel method.)
1694,10.1002/bio.2956,sol_gel_ceramic_synthesis,"The detailed experimental procedures of the EDTA s ...  references on similar YVO4:Eu3+ systems [16, 17]."
1695,10.1016/j.jpowsour.2008.04.012,sol_gel_ceramic_synthesis,The (BS)1-xCF oxide powders were synthesized via a ... ducts possessed the desired final phase structure.
1696,10.1016/j.elecom.2012.03.001,sol_gel_ceramic_synthesis,LSMC powder was synthesized by a modified sol-gel  ... ynthesized using the glycine-nitrate process [21].
1697,10.1016/j.jeurceramsoc.2015.01.012,sol_gel_ceramic_synthesis,"As to the sol-gel method, the typical experimental ... Ceramics were also sintered at 1600 degC for 10 h."
1698,10.1016/j.electacta.2010.08.033,sol_gel_ceramic_synthesis,Citric acid and SnCl4*5H2O in a molar ratio of 2:1 ... r structural analyses and electrochemical testing.
1699,10.1016/j.jpowsour.2010.10.065,sol_gel_ceramic_synthesis,"LiFePO4/C material was synthesized with a novel so ... lly, LiFePO4/C submicrometer-crystal was obtained."
1700,10.1007/s10853-011-5514-8,sol_gel_ceramic_synthesis,"On the other hand, Pd-Fe-Ox/Al2O3 catalyst was pre ... prepared was designated as sol-gel-Pd-Fe-Ox/Al2O3."
1701,10.1002/ejic.201300430,sol_gel_ceramic_synthesis,Preparation: Ca9MgNa(PO4)7:Ce3+/Tb3+/Mn2+ samples  ... 2/90 % N2 atmosphere to produce the final samples.
1702,10.1016/j.matchemphys.2004.11.030,sol_gel_ceramic_synthesis,The process of sample nanometer crystalline TiO2 f ... ained by calcining the powders at 600degC for 4 h.
1703,10.1016/j.jpowsour.2004.02.016,sol_gel_ceramic_synthesis,"LiCrxMn2-xO4 (x=0.00, 0.01, 0.02, 0.05, 0.10, 0.20 ... sical as well as electrochemical characterization."
1704,10.1016/j.scriptamat.2011.02.029,sol_gel_ceramic_synthesis,"To make Y2O3-MgO nanocomposite powder, ultrahigh-p ... degC) in air in a furnace and powder was obtained."
1705,10.1016/j.mseb.2009.02.007,sol_gel_ceramic_synthesis,Powder of Gd2BaCuO5 was synthesized by sol-gel pro ... l experiments were conducted with CA or EDTA only.
1706,10.1016/j.jpcs.2014.01.005,sol_gel_ceramic_synthesis,Fe-substituted Ca3Co4O9 powder was prepared from a ... ds at temperatures lower than 1193 K is necessary.
1707,10.1016/j.jpowsour.2015.03.027,sol_gel_ceramic_synthesis,"SmxSr1-xMnO3 (SSM) powders with x = 0.3, 0.5 and 0 ... fined by the Rieltveld method using GSAS software."
1708,10.1016/j.mseb.2010.11.012,sol_gel_ceramic_synthesis,"BiFe1-xCrxO3 (x = 0, 0.04, 0.06 and 0.08) nanocera ... ce as a function of magnetic field also presented."
1709,10.1016/j.apcata.2004.05.002,sol_gel_ceramic_synthesis,Ceria-zirconia mixed metal oxides (Ce-Zr-O) were p ... ed to room temperature and stored for further use.
1710,10.1007/s10853-011-6139-7,sol_gel_ceramic_synthesis,The FePO4 was synthesized by a sol-gel combustion  ... C for 8 h in a N2/H2 (90/10 in volume) atmosphere.
1711,10.1016/j.electacta.2005.09.023,sol_gel_ceramic_synthesis,Commercially LiCoO2 powder (SEIMI Chemical Co.) wa ...  to 200 degC h-1 for all the temperature settings.
1712,10.1016/j.jallcom.2006.10.126,sol_gel_ceramic_synthesis,Lithium samarium silicate (LiSmSiO4) was prepared  ... ned by calcining the powders at 800 degC for 24 h.
1713,10.1016/j.jpowsour.2010.08.106,sol_gel_ceramic_synthesis,The precursor Na2Ti6O13 was prepared by two differ ... was ground and heated at 925 degC for 36 h in air.
1714,10.1016/j.jssc.2016.01.002,sol_gel_ceramic_synthesis,Pure TiO2 was synthesized by the sol-gel method. W ... at 500 degC for 1 h to obtain the final specimens.
1715,10.1002/ep.10549,sol_gel_ceramic_synthesis,The sol-gel method was used to deposit TiO2 onto t ... ated as BT-h where h is the annealing temperature.
1716,10.1016/j.matlet.2014.11.111,sol_gel_ceramic_synthesis,"The single phase multiferroic BFO, BDFCO and BDFO  ... ment of magnetoelectric effect of all the samples."
1717,10.1016/j.matchemphys.2003.11.012,sol_gel_ceramic_synthesis,"In our study, the sol-gel method known for its adv ... hen treated at 430 and 500 degC under oxygen flow."
1718,10.1016/j.polymdegradstab.2012.05.022,sol_gel_ceramic_synthesis,"Titania was prepared by the sol-gel combustion of  ... of the powders were black and white, respectively."
1719,10.1016/j.matlet.2015.01.038,sol_gel_ceramic_synthesis,xBSFMO films with x=0.00-0.09 were deposited on th ... everal times to obtain the desired film thickness.
1720,10.1016/j.jssc.2004.11.015,sol_gel_ceramic_synthesis,Nanosized-Ta2O5 powder photocatalyst was successfu ... catalytical performance of nanosized-Ta2O5 powder.
1721,10.1016/j.cattod.2011.03.004,sol_gel_ceramic_synthesis,"Co doping ceria mixed oxides (CoxCe1-xOy, x = 0.01 ... pared with the same method were reference samples."
1722,10.1016/j.jpowsour.2014.03.061,sol_gel_ceramic_synthesis,"The Li3V1.8Mn0.2(PO4)3 composites (LVMP) were prep ... , MnOOH, Mn3O4 and (CH3COO)2Mn*4H2O, respectively."
1723,10.1016/j.jallcom.2007.09.002,sol_gel_ceramic_synthesis,Tb4O7 (99.99%) and Gd2O3 (99.99%) were dissolved i ... ed on a high-temperature oven at 900 degC for 5 h.
1724,10.1016/j.jpowsour.2012.10.033,sol_gel_ceramic_synthesis,The LiNi1/3Mn1/3Co1/3O2 compound was prepared by t ...  times and dried in the vacuum oven under 80 degC.
1725,10.1016/j.jpowsour.2015.09.127,sol_gel_ceramic_synthesis,Pr0.5Ba0.5MnO3-δ with and without 10 mol% Mo dopan ... phase based on our previous experiment experience.
1726,10.1016/j.electacta.2012.03.181,sol_gel_ceramic_synthesis,"The ferric citrate (FeC6H5O7*5H2O), V2O5, Li2CO3,  ... red via the same process without addition of V2O5."
1727,10.1016/j.jallcom.2012.08.064,sol_gel_ceramic_synthesis,"The samples of Ni0.5Zn0.5ZrxFe2-xO4 (x = 0, 0.05,  ... n ferrite thin films is about 518 nm (see Fig. 1)."
1728,10.1016/j.electacta.2009.05.034,sol_gel_ceramic_synthesis,"A sol-gel process was used to prepare the ZnO-coat ... marked as ZnO-05, ZnO-15 and ZnO-30, respectively."
1729,10.1016/j.jcat.2016.04.013,sol_gel_ceramic_synthesis,"Samples were prepared by a sol-gel method using et ... denoted as La1-xCexCoO3 (x = 0, 0.05, 0.10, 0.15)."
1730,10.1016/j.optmat.2013.06.009,sol_gel_ceramic_synthesis,"In the present investigation, the samples with nom ... ir atmosphere for 4 h followed by furnace cooling."
1731,10.1016/j.optmat.2011.04.020,sol_gel_ceramic_synthesis,"Nano-crystalline cubic spinel, pure MgAl2O4 and do ... MgAl2O4 and doped with Tb3+ ions have been formed."
1732,10.1016/j.jssc.2010.10.025,sol_gel_ceramic_synthesis,Silicate oxy-apatites Sr2Y8-xEux(SiO4)6O2 (x=0.05- ...  until the apatite powder materials were obtained.
1733,10.1002/jssc.201400256,sol_gel_ceramic_synthesis,"Transition metal precursor is hydrolyzed with wate ... alcined at 450 and 400degC, respectively [98, 99]."
1734,10.1016/j.jeurceramsoc.2012.03.004,sol_gel_ceramic_synthesis,The BaCe0.95Tb0.05O3-α (BCTb) perovskite powder wa ... ough a sifter of 200-mesh to exclude agglomerates.
1735,10.1016/j.cattod.2008.08.007,sol_gel_ceramic_synthesis,Ag/γ-Al2O3 was prepared by a single-step sol-gel m ... r later use. γ-Al2O3 was prepared in the same way.
1736,10.1016/j.jeurceramsoc.2008.08.016,sol_gel_ceramic_synthesis,The Bi1-xCexFeO3 (BCFO) films were prepared on LaN ... ted several times to obtain the desired thickness.
1737,10.1016/j.electacta.2007.02.078,sol_gel_ceramic_synthesis,To prepare the crystalline LiMn2O4 powder by the s ... degC for 5 h and then at 800 degC for 24 h in air.
1738,10.1016/j.electacta.2015.05.171,sol_gel_ceramic_synthesis,"0.5Li2MnO3*0.5LiNi0.5Co0.2Mn0.3O2, labeled as GLLM ...  heating the precursor at 900degC for 12 h in air."
1739,10.1016/j.optmat.2015.01.018,sol_gel_ceramic_synthesis,Ba2Ca1-xMoO6:xEu3+ phosphors with different Eu3+ d ... r 5 h in air to obtain the yellow phosphor sample.
1740,10.1016/j.electacta.2016.05.075,sol_gel_ceramic_synthesis,"A facile sol-gel method was employed to achieve th ...  0 wt.%, 1 wt.%, 2 wt.%, and 4 wt.%, respectively."
1741,10.1016/j.apenergy.2016.04.046,sol_gel_ceramic_synthesis,Mixed oxides with a general formula of CaMn1-xBxO3 ... s crushed and sieved to under 90 μm particle size.
1742,10.1016/j.jmmm.2013.03.027,sol_gel_ceramic_synthesis,Ni0.5-xMgxCu0.05Zn0.45Fe2O4 nanoparticles were pro ... te of 2 degC/min in a programmable muffle furnace.
1743,10.1016/j.matchemphys.2010.10.031,sol_gel_ceramic_synthesis,"Gd1-xSrxCoO3-δ (x = 0.0, 0.25, 0.5 and 0.75) sampl ...  h at 700-1200 degC with an intermediate grinding."
1744,10.1016/j.jpowsour.2014.02.011,sol_gel_ceramic_synthesis,"As a comparison, Li-rich compound with the same co ... mplate and sol-gel method for short, respectively."
1745,10.1016/j.jpowsour.2015.04.181,sol_gel_ceramic_synthesis,"In this context, CoO with a 3D-Network macro-porou ... C under Ar/H2 (95:5 by volume) atmosphere for 4 h."
1746,10.1016/j.ssi.2005.07.018,sol_gel_ceramic_synthesis,"Ce0.8M0.2O2-δ (M = La, Y, Gd, Sm) powder was prepa ... r at 1450 degC for 10 h to prepare ceramic sample."
1747,10.1007/s10854-016-5464-7,sol_gel_ceramic_synthesis,"The perovskite Ca0.925Ce0.075Mn1-xFexO3 (x = 0.1,  ... d at 800 degC for 5 h to obtain the final product."
1748,10.1016/j.electacta.2014.03.171,sol_gel_ceramic_synthesis,LiMnPO4 was prepared by a sol-gel method based on  ...  sample was 600 degC and the reaction time is 5 h.
1749,10.1016/j.nanoen.2016.01.031,sol_gel_ceramic_synthesis,The LiFePO4/C composites were obtained through a s ...  N2 atmosphere to obtain the LiFePO4/C composites.
1750,10.1016/j.electacta.2014.02.026,sol_gel_ceramic_synthesis,Li2CoPO4F was synthesized by two-step process comb ... llowed by the natural cooling to room temperature.
1751,10.1016/j.materresbull.2010.11.026,sol_gel_ceramic_synthesis,"Analytical grade chromium nitrate [Cr(NO3)3*9H2O], ... o remove out the volatile organic binder material."
1752,10.1007/s10854-015-3068-2,sol_gel_ceramic_synthesis,"The synthesis of Ba(CuTi)xFe12-2xO19 (x = 0, 0.5,  ... ically pure and used without further purification."
1753,10.1016/j.matchemphys.2015.07.063,sol_gel_ceramic_synthesis,The synthesis process of graphene/SrFe12O19 nanoco ... rformances of such material to the REGO/SrFe12O19.
1754,10.1016/j.materresbull.2014.04.010,sol_gel_ceramic_synthesis,"Nanocrystalline anatase TiO2 codoped with Y and F  ... also prepared by similar procedures, respectively."
1755,10.1016/j.jssc.2013.12.009,sol_gel_ceramic_synthesis,"CaCu3Ti4O12 precursor was prepared via a simple so ... s, thin tablets of 0.2-0.5 mm thick were prepared."
1756,10.1016/j.ssi.2007.12.071,sol_gel_ceramic_synthesis,"The third method was based on the sol-gel process  ... impurity. We name this sample ""LFP3"" in this work."
1757,10.1016/j.mssp.2014.02.041,sol_gel_ceramic_synthesis,"In the sol-gel method, titanium (IV) chloride (50  ... C) to get the pure anatase phase of TiO2 material."
1758,10.1016/j.matlet.2009.01.070,sol_gel_ceramic_synthesis,"Ceria preparation with the new method includes two ... 393-1253 K) for 4 h, and termed as N(x)Tc/Ta-CeO2."
1759,10.1016/j.electacta.2014.11.138,sol_gel_ceramic_synthesis,"The spinel Li2MnTi3O8 was prepared by using a one- ... . As a result, the spinel Li2MnTi3O8 was obtained."
1760,10.1016/j.apsusc.2007.02.113,sol_gel_ceramic_synthesis,The Er:YAG powder was obtained by a nitrate-citrat ...  pellet shape and thermally sintered at 1400 degC.
1761,10.1016/j.apsusc.2014.11.056,sol_gel_ceramic_synthesis,"Ce0.2Co0.2Ti, Co0.2Ti and Ce0.2Ti mixed oxide cata ... Ti, 0.2 meant the molar ratio of Ce/Ti (or Co/Ti)."
1762,10.1016/j.matlet.2014.05.167,sol_gel_ceramic_synthesis,ZnFe2O4 was synthesized via sol-gel method using s ...  sensing material and we labeled this film as G-1.
1763,10.1016/j.jeurceramsoc.2005.03.239,sol_gel_ceramic_synthesis,PLT powder and BST powders with compositions of Ba ... its melting point temperature is below 650 degC.15
1764,10.1016/j.ssi.2012.12.007,sol_gel_ceramic_synthesis,Precursors for the nominal chemical formula Li7La3 ... ating at 800 degC for 20 h in an alumina crucible.
1765,10.1016/j.nanoen.2011.10.003,sol_gel_ceramic_synthesis,Ca2Mn3O8 and Ca2MnO4 dipping solutions were prepar ... intained at this temperature for two hours in air.
1766,10.1016/j.electacta.2015.07.095,sol_gel_ceramic_synthesis,"Typically, V2O5 and oxalic acid in a stoichiometri ... uced Li3V2(PO4)3/carbon was simply named as LVP/C."
1767,10.1016/j.electacta.2012.10.048,sol_gel_ceramic_synthesis,"The LixCoPO4 (x = 0.90, 0.95, 1, 1.05) compounds w ... ame atmosphere to obtain the final purple powders."
1768,10.1016/j.jmmm.2015.10.078,sol_gel_ceramic_synthesis,Ce-substituted yttrium iron garnet (Ce-YIG) films  ... 00 sccm. This process is to crystallize the films.
1769,10.1016/j.apenergy.2015.04.020,sol_gel_ceramic_synthesis,Mixed oxides with a general formula of Ca1-xAxMnO3 ... s crushed and sieved to under 75 μm particle size.
1770,10.1007/s10854-011-0379-9,sol_gel_ceramic_synthesis,BFO nanowires with 100-200 nm length and of 8-10 n ... samples were annealing for 2 h in air at 400 degC.
1771,10.1016/j.jpowsour.2008.09.116,sol_gel_ceramic_synthesis,"Nanocrystalline LSM powders were prepared by a mod ... EG, PVA and EG) and pH value of 1 and 3 were used."
1772,10.1016/j.ssi.2010.08.022,sol_gel_ceramic_synthesis,"As an additional point of reference, high-quality  ... BCY20-SG) with a relative density higher than 90%."
1773,10.1016/j.jpowsour.2012.02.110,sol_gel_ceramic_synthesis,"The Li3V2(PO4)3-xClx/C (x = 0, 0.04, 0.08, 0.12 an ...  hydrochloric acid and the remaining was weighted."
1774,10.1007/s10853-006-0417-9,sol_gel_ceramic_synthesis,The YSI powders were prepared by a modified Pechin ... already obtained crystalline powders at 1100 degC.
1775,10.1016/j.sse.2007.04.010,sol_gel_ceramic_synthesis,Nanostructured WO3 powder were synthesized using s ... ed mass was ground for 4 h to get the WO3 powders.
1776,10.1016/j.jnoncrysol.2016.05.010,sol_gel_ceramic_synthesis,Hydroxyapatite [Ca10(PO4)6(OH)2] was prepared from ... round using mortar and pestle to obtain powder HA.
1777,10.1016/j.jpowsour.2014.07.138,sol_gel_ceramic_synthesis,The cathode materials of LFP and LFPV were obtaine ... tered at 800 degC for 12 h in nitrogen atmosphere.
1778,10.1016/j.matlet.2007.10.003,sol_gel_ceramic_synthesis,The chemical agents used in this experiment were a ...  a ramp rate of 1 degC/min up to 800 degC for 3 h.
1779,10.1016/j.cattod.2014.05.042,sol_gel_ceramic_synthesis,Ce0.33Zr0.67O2 (denoted as CeZr) mixed oxides were ... ina also experienced the same calcination process.
1780,10.1016/j.solmat.2010.03.011,sol_gel_ceramic_synthesis,Preparation of Nb-TiO2sol-gel: Stoichiometric amou ...  dense layers were about 100 nm when used for HSC.
1781,10.1016/j.jallcom.2014.04.193,sol_gel_ceramic_synthesis,"The strontium powders were synthesized by sol-gel  ... 00 degC, 850 degC, and 900 degC for different tca."
1782,10.1016/j.matchemphys.2011.04.081,sol_gel_ceramic_synthesis,The BNT films were prepared by a sol-gel method. T ... above corresponding annealing temperatures in air.
1783,10.1016/j.cattod.2010.01.050,sol_gel_ceramic_synthesis,Various Ce-Zr-Ni-Me catalysts were prepared by pse ... f as prepared catalysts are summarized in Table 1.
1784,10.1016/j.cej.2013.03.022,sol_gel_ceramic_synthesis,"The catalyst was prepared by sol-gel method [3]. B ...  was 0.1, and the molar ratio of Mn to Ti was 0.4."
1785,10.1016/j.jallcom.2012.11.149,sol_gel_ceramic_synthesis,"The Sm3+-doped TiO2 nanoparticles were synthesized ...  mol%, in which x = 0 means the pure TiO2 samples."
1786,10.1016/j.jpowsour.2015.05.110,sol_gel_ceramic_synthesis,A commercially available carbon coated LiFePO4 (LF ... PO4 sample which is labeled hereafter as C-LFP-SG.
1787,10.1002/adfm.201401006,sol_gel_ceramic_synthesis,In order to further confirm and verify the modific ... Ti5O12/C+B just without the addition of NaBC24H20.
1788,10.1016/j.ijhydene.2010.11.071,sol_gel_ceramic_synthesis,A series of several mixed oxides close to NiAl2O4  ... ric spinel calcinated at 900 degC will be noted S.
1789,10.1007/s10854-010-0108-9,sol_gel_ceramic_synthesis,Pure and Nd doped BaTiO3 were prepared by sol gel  ...  air at 1250 degC for 3 h to yield dense ceramics.
1790,10.1016/j.apenergy.2015.01.131,sol_gel_ceramic_synthesis,The 1-5 wt.%LTO-coated SP-LFP/C composites were sy ...  obtain the final 3%LTO-coated SP-LFP/C composite.
1791,10.1016/j.apenergy.2016.02.120,sol_gel_ceramic_synthesis,"The CaO-based, Fe-functionalized CO2 sorbents were ... he molar ratio of CA to the total metal ions (Me)."
1792,10.1016/j.solidstatesciences.2011.11.008,sol_gel_ceramic_synthesis,"Composites with Al2O3 composition (mole) of x = 0. ... btained was a voluminous, fluffy and brown powder."
1793,10.1016/j.jlumin.2015.08.068,sol_gel_ceramic_synthesis,"Eu3+-doped Nb2O5 nanostructured particles were pre ... ed and annealed at 600, 900 and 1100 degC for 8 h."
1794,10.1016/j.jpowsour.2013.11.037,sol_gel_ceramic_synthesis,"The La-M-Cu-Zn-O (M = Y, Ce, Mg, Zr) perovskite-ty ...  LMCZ-8273, LCCZ-8273 and LZCZ-8273, respectively."
1795,10.1016/j.jcis.2006.12.005,sol_gel_ceramic_synthesis,"The Ce1-xCuxO2-y mixed oxide samples, where the Cu ... cancies in non-stoichiometric CeO2-y nanocrystals."
1796,10.1016/j.matlet.2007.09.053,sol_gel_ceramic_synthesis,"Lutetium gallium garnet (Lu3Ga5O12, LGG) samples w ...  the Lu3Ga5O12 garnet ceramics is shown in Fig. 1."
1797,10.1016/j.mseb.2005.10.006,sol_gel_ceramic_synthesis,Amorphous and polycrystalline Pb(ZrxTi(1-x))O3 thi ... s were pre-annealed at 350 degC in air for 10 min.
1798,10.1016/j.matchemphys.2016.11.013,sol_gel_ceramic_synthesis,HA nanopowder was synthesized using sol-gel method ... posed to TCP during sintering at high temperature.
1799,10.1016/j.cej.2012.10.036,sol_gel_ceramic_synthesis,"Firstly, TiO2 powder was synthesized using a sol-g ...  300 degC for 2 h to acquire CN co-doped TiO2 NTs."
1800,10.1016/j.matlet.2015.09.110,sol_gel_ceramic_synthesis,"Lanthanum acetate (99.9%, Alfa Aesar) and nickel a ... with the final heating step at 1400 degC for 24 h."
1801,10.1016/j.fuel.2015.11.012,sol_gel_ceramic_synthesis,Catalysts were prepared through sol-gel method. Ni ... ained solid product was sieved in a 50-mesh sieve.
1802,10.1016/j.jpowsour.2013.05.115,hydrothermal_ceramic_synthesis,"Initially, α-MnO2 nanotubes were prepared by a sli ... C for 24 h [26]; this sample was designated S-LMO."
1803,10.1002/chem.200903137,hydrothermal_ceramic_synthesis,Preparation of CaF2and CaF2:Ce3+/Tb3+hollow sphere ... orphological evolution of the CaF2 hollow spheres.
1804,10.1016/j.electacta.2015.08.044,hydrothermal_ceramic_synthesis,The scheme of the synthesis process of NiO-Co3O4 n ... hout the addition of NiO nanoplate for comparison.
1805,10.1016/j.jpcs.2014.09.002,hydrothermal_ceramic_synthesis,"All chemicals were analytic grade and used without ... Bi2MoO6:1BiPO4, and 1Bi2MoO6:2BiPO4, respectively."
1806,10.1016/j.apcatb.2015.06.061,hydrothermal_ceramic_synthesis,Different hematite architectures were synthesized  ... -1 in air to obtain the hematite nanorods for use.
1807,10.1016/j.materresbull.2012.04.074,hydrothermal_ceramic_synthesis,Sample 1 was prepared as the following: In a typic ... ing 6.6 molar% of Y(NO3)3*6H2O with Eu(NO3)3*6H2O.
1808,10.1016/j.electacta.2016.01.008,hydrothermal_ceramic_synthesis,All chemicals were used as received without furthe ... t 60 degC to obtain the final product of MnMoO4@C.
1809,10.1016/j.apenergy.2015.11.038,hydrothermal_ceramic_synthesis,"Nanostructured Bi2Te3 and Sb2Te3 were synthesized  ... gation, and it was washed three times using water."
1810,10.1016/j.jallcom.2016.04.209,hydrothermal_ceramic_synthesis,Li4Ti5O12 powders were synthesized by a hydrotherm ...  same procedure with glucose as the carbon source.
1811,10.1016/j.jpowsour.2016.02.082,hydrothermal_ceramic_synthesis,"In a typical synthesis, 1 mL of tetrabutyl titanat ... or 1 h with a ramping rate of 3 degC min-1 in air."
1812,10.1007/s10854-016-5481-6,hydrothermal_ceramic_synthesis,MnO2 nanorods were synthesized by using a simple s ... he resulting product was dried at 60 degC for 2 h.
1813,10.1016/j.matlet.2014.04.160,hydrothermal_ceramic_synthesis,The core-shell SnO2@TiO2-B nanowires were synthesi ... d after being annealed in air at 360 degC for 4 h.
1814,10.1007/s10854-015-3995-y,hydrothermal_ceramic_synthesis,"In a typical hydrothermal synthesis, 0.291 g Co(NO ... 0 degC for 3 h in air to produce Co3O4 nanosheets."
1815,10.1007/s10008-016-3373-6,hydrothermal_ceramic_synthesis,All chemical reagents were of analytical grade wit ... 80 degC overnight to obtain Bi3.64Mo0.36O6.55 NPs.
1816,10.1016/j.mseb.2009.04.013,hydrothermal_ceramic_synthesis,All the chemical reagents used in this experiment  ...  replacing 5% molar Y(NO3)3*6H2O by Eu(NO3)3*6H2O.
1817,10.1016/j.jssc.2014.03.032,hydrothermal_ceramic_synthesis,The BiOBr/K2La2Ti3O10 sample was synthesized throu ... ve its crystallinity and remove residual organics.
1818,10.1016/j.snb.2009.06.049,hydrothermal_ceramic_synthesis,Hollow sea urchin-like α-Fe2O3 nanostructures: In  ... as used for further analysis and characterization.
1819,10.1016/j.jpowsour.2012.07.105,hydrothermal_ceramic_synthesis,"TiO2 hollow spheres with {001} facets exposed (TiO ...  2 degC min-1, resulting the formation of TiO2-HS."
1820,10.1016/j.molcata.2015.02.020,hydrothermal_ceramic_synthesis,"A simple solvothermal method was used to synthesiz ... 5, C/ZIS-0.1, C/ZIS-0.5, C/ZIS-0.7, were obtained."
1821,10.1002/adfm.201303508,hydrothermal_ceramic_synthesis,"Preparation of MnO2 Nanostructures: MnO2 nanostruc ... ly, the products were dried in an oven at 80 degC."
1822,10.1016/j.matlet.2012.09.078,hydrothermal_ceramic_synthesis,"Sample preparation: Synthesis of Ag2WO4/AgCl nanor ... nol for three times, and dried at 60 degC for 4 h."
1823,10.1016/j.cej.2016.12.005,hydrothermal_ceramic_synthesis,"First, C@NiCo2O4 composites were prepared by one s ... C/min, and then C@NiCo2O4 composites was obtained."
1824,10.1016/j.ijhydene.2015.11.087,hydrothermal_ceramic_synthesis,(CuIn)0.2Zn1.6S2 (CIZS) samples were prepared via  ... ed grams of added TAA in the hydrothermal process.
1825,10.1016/j.apsusc.2011.07.010,hydrothermal_ceramic_synthesis,"In a typical synthesis, 2 mmol of Ce(NO3)3*6H2O an ... atures (80-150 degC), and reaction times (6-36 h)."
1826,10.1016/j.matlet.2010.09.079,hydrothermal_ceramic_synthesis,All chemicals used in this work were of analytic p ...  at room temperature for further characterization.
1827,10.1016/j.jallcom.2014.02.083,hydrothermal_ceramic_synthesis,"Pr, N, P-tridoped TiO2 nano-photocatalyst was synt ... he Pr, N, P-tridoped sample was denoted as PrNPTO."
1828,10.1016/j.solidstatesciences.2013.03.006,hydrothermal_ceramic_synthesis,"In a typical reaction process, 0.15 g copper aceta ... at 600 degC (heating rate of 20 degC/min) for 2 h."
1829,10.1016/j.jpowsour.2013.10.046,hydrothermal_ceramic_synthesis,All the reagents are of analytical purity grade an ... r 1 h in air with a ramping rate of 10 degC min-1.
1830,10.1016/j.matchemphys.2005.08.024,hydrothermal_ceramic_synthesis,"The ZnGa2O4 nanocrystalline samples were prepared  ... l times, and then dried in air at 60 degC for 4 h."
1831,10.1016/j.snb.2010.12.036,hydrothermal_ceramic_synthesis,"All chemical reagents purchased from Beijing Chemi ... temperature, the reaction products were collected."
1832,10.1016/j.ijhydene.2013.03.145,hydrothermal_ceramic_synthesis,The typical synthesis of NiSe hollow nanospheres i ... ed sample was dried in vacuum at 60 degC for 12 h.
1833,10.1007/s10854-008-9813-z,hydrothermal_ceramic_synthesis,"In a typical synthesis, appropriate amounts of hig ... ed at 80 degC in air for further characterization."
1834,10.1016/j.scriptamat.2012.07.010,hydrothermal_ceramic_synthesis,"The SnO nanoflowers and nanopetals were synthesize ...  12 h, and collected for further characterization."
1835,10.1016/j.ijhydene.2012.04.158,hydrothermal_ceramic_synthesis,"The precipitated amorphous titanium precursor was  ... led samples as TNT400 and Fe-TNT400, respectively."
1836,10.1016/j.matchemphys.2012.07.044,hydrothermal_ceramic_synthesis,In a typical synthesis of cube-like hierarchical Z ... ed at 60 degC in air for further characterization.
1837,10.1016/j.molcata.2011.08.023,hydrothermal_ceramic_synthesis,"All of the reagents were of analytical grade and u ... r several times, and then dried in air at 80 degC."
1838,10.1016/j.apsusc.2007.05.067,hydrothermal_ceramic_synthesis,"In a typical synthesis process, 0.008 mol zinc ace ... lected for further characterization and treatment."
1839,10.1002/chem.201203437,hydrothermal_ceramic_synthesis,Preparation of Bi2Te3 nanorod bundles: In a typica ... and finally dried under vacuum at 60 degC for 4 h.
1840,10.1002/smll.201400239,hydrothermal_ceramic_synthesis,Synthesis of Fe3O4/C Microrods and Fe3O4 Nanospher ... rimental conditions except the absence of glucose.
1841,10.1016/j.matlet.2015.08.129,hydrothermal_ceramic_synthesis,All the reagents were of analytic purity and used  ...  at 400 degC for 2 h to obtain the final products.
1842,10.1016/j.matchemphys.2013.05.048,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade reagents an ... ed at 80 degC for 24 h to obtain the final sample.
1843,10.1016/j.matdes.2016.02.103,hydrothermal_ceramic_synthesis,"Three MnxFe3 - xO4 samples (denoted as MFO-1, MFO- ... , MFO-3 were 9.3, 18.5, and 37 mmol, respectively."
1844,10.1016/j.jallcom.2015.03.172,hydrothermal_ceramic_synthesis,Zn2SnO4@C core-shell nanorods were prepared by a h ... or 3 h under N2 at a ramping rate of 5 degC min-1.
1845,10.1016/j.electacta.2013.10.188,hydrothermal_ceramic_synthesis,"Porous Fe2O3 microspheres were prepared through a  ... or 10 min, and finally cooled to room temperature."
1846,10.1016/j.matlet.2010.04.045,hydrothermal_ceramic_synthesis,"Initially, 14.2 mmol of ascorbic acid (C6H8O6) and ... water and ethanol, then dried at 60 degC for 12 h."
1847,10.1016/j.snb.2013.02.031,hydrothermal_ceramic_synthesis,"Experimental details were as follows: Na2WO4*2H2O  ...  water three times, and dried at 50 degC for 24 h."
1848,10.1016/j.matlet.2004.09.037,hydrothermal_ceramic_synthesis,"In the typical hydrothermal synthesis, 0.001 mol S ... nal products, and finally dried at 80 degC in air."
1849,10.1007/s00339-013-7896-8,hydrothermal_ceramic_synthesis,"N,W codoped TiO2 nanorods were synthesized by a on ... n of ammonium metatungstate using the same method."
1850,10.1016/j.jpowsour.2015.10.109,hydrothermal_ceramic_synthesis,"As for the hollow TiO2 microspheres, titanium n-bu ...  at 60 degC to get the synthesized powder samples."
1851,10.1016/j.electacta.2012.01.010,hydrothermal_ceramic_synthesis,"In a typical procedure for synthesizing flower-lik ... pectively, and dried in vacuum at 60 degC for 4 h."
1852,10.1016/j.mseb.2008.11.008,hydrothermal_ceramic_synthesis,"Y0.95Eu0.05VO4 powders were prepared via surfactan ... al times, and dried in vacuum at 80 degC for 10 h."
1853,10.1016/j.jssc.2015.04.043,hydrothermal_ceramic_synthesis,"In a typical process, 0.77 mmol of CoCl2*6H2O was  ... 00 degC for 2 h with a heating rate of 2 degC/min."
1854,10.1002/crat.201500039,hydrothermal_ceramic_synthesis,All reagents were of analytical grade and used as  ... thod under the same conditions as mentioned above.
1855,10.1016/j.electacta.2012.04.094,hydrothermal_ceramic_synthesis,"In a typical synthesis, titanium (IV) n-butoxide ( ... muffle furnace at 500 degC for 4 h (5 degC min-1)."
1856,10.1016/j.matchemphys.2008.08.023,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade and used wi ... vely and finally dried in air at room temperature.
1857,10.1007/s10854-012-0926-z,hydrothermal_ceramic_synthesis,"In a typical experiment, 1 mmol (0.1997 g) of copp ... nd ethanol at a volume ratio of 1:1, respectively."
1858,10.1007/s10854-015-3444-y,hydrothermal_ceramic_synthesis,The NF-SnO2 particles were prepared from the hydro ... he precipitates at 500 degC for 2.5 h in air [18].
1859,10.1016/j.matlet.2015.02.027,hydrothermal_ceramic_synthesis,"Synthesis: All of the chemical reagents were of an ... , and finally dried in vacuum at 60 degC for 24 h."
1860,10.1016/j.apcatb.2012.04.018,hydrothermal_ceramic_synthesis,"In synthesizing SnS2/TiO2 nanocomposites, 3.0 mmol ... ed water, and dried in vacuum at 100 degC for 4 h."
1861,10.1016/j.electacta.2016.06.015,hydrothermal_ceramic_synthesis,All the materials used in this work were of analyt ...  in a vacuum and collected for the following used.
1862,10.1016/j.biortech.2015.06.054,hydrothermal_ceramic_synthesis,All of the starting materials were in analytical g ...  heated at 300 degC for 3 h in the muffle furnace.
1863,10.1016/j.mseb.2013.01.024,hydrothermal_ceramic_synthesis,The bud-like FeS2 microshperes were synthesized by ... s also obtained by the same method for comparison.
1864,10.1016/j.cattod.2016.05.042,hydrothermal_ceramic_synthesis,Uniform CdS NSPs were synthesized by a simple hydr ... ed CdS NSPs were further dried at 70 degC for 5 h.
1865,10.1016/j.powtec.2008.07.007,hydrothermal_ceramic_synthesis,"All the reagents were purchased from the local mar ... 8 h in the presence of 3 mL PEG-300, respectively."
1866,10.1016/j.matlet.2011.03.056,hydrothermal_ceramic_synthesis,"All chemicals used were analytical grade reagents. ... mes, and then dried in vacuum at 60 degC for 12 h."
1867,10.1016/j.matlet.2005.06.057,hydrothermal_ceramic_synthesis,All the chemicals were analytic grade reagents wit ... and finally dried in a vacuum at 40 degC for 72 h.
1868,10.1016/j.matlet.2016.04.157,hydrothermal_ceramic_synthesis,"In typical synthesis, 2/3 mmol of Mn(CH3COO)2 4H2O ... min-1. Then, the final black product was obtained."
1869,10.1016/j.electacta.2011.12.058,hydrothermal_ceramic_synthesis,TiOF2 nanocubes with edge length of 200-300 nm wer ... t of no acetic acid is similar to above procedure.
1870,10.1016/j.apsusc.2016.03.025,hydrothermal_ceramic_synthesis,CNNS/CQDs were prepared by a simple process in whi ... down to room temperature and vacuum-dried for 2 h.
1871,10.1016/j.colsurfa.2011.12.058,hydrothermal_ceramic_synthesis,"In a typical route, 1.0-4.0 g of d-(+)-glucose (C6 ...  degC for future characterization and application."
1872,10.1016/j.matlet.2015.07.133,hydrothermal_ceramic_synthesis,A typical synthesis procedure of the porous CuO he ... ipitates were then calcinated at 500 degC for 4 h.
1873,10.1007/s10853-010-4505-5,hydrothermal_ceramic_synthesis,All chemicals of analytical grade were used as rec ... were dried in an electric oven at 60 degC for 6 h.
1874,10.1016/j.jallcom.2015.03.103,hydrothermal_ceramic_synthesis,"All chemicals were analytical purity and used with ... e value of 0.00, 0.03, 0.07 and 0.10 respectively."
1875,10.1016/j.spmi.2015.11.012,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.97 mmol of La(NO3)3*6H2O ... lly, the production was dried at 60 degC for 12 h."
1876,10.1016/j.electacta.2014.05.118,hydrothermal_ceramic_synthesis,All reagents are of analytical grade and used with ... the octahedron-shaped CoS2 crystals were obtained.
1877,10.1016/j.matchemphys.2007.06.061,hydrothermal_ceramic_synthesis,All the reagents are of analytical purity grade an ... mples were collected for further characterization.
1878,10.1007/s10854-016-4986-3,hydrothermal_ceramic_synthesis,All the reagents were of analytic purity and used  ...  degC min-1 and then calcined at 400 degC for 4 h.
1879,10.1016/j.matlet.2013.02.103,hydrothermal_ceramic_synthesis,"Synthesis of MoS2samples: All chemical reagents we ... s, and finally dried in vacuum at 80 degC for 8 h."
1880,10.1007/s10854-014-2490-1,hydrothermal_ceramic_synthesis,"The typical procedure is as follows: First, 0.04 m ... veral times, and dried at room temperature in air."
1881,10.1002/adfm.200901503,hydrothermal_ceramic_synthesis,In a typical synthesis of the precursor cobalt hyd ... d in a desiccator before further characterization.
1882,10.1016/j.cej.2013.10.079,hydrothermal_ceramic_synthesis,All reagents used were of analytical purity and we ... ltant samples were collected for characterization.
1883,10.1016/j.jpcs.2016.01.009,hydrothermal_ceramic_synthesis,The novel photocatalyst Ag+/BiVO4 was prepared via ... detailed reaction conditions are shown in Table 1.
1884,10.1016/j.jhazmat.2011.01.078,hydrothermal_ceramic_synthesis,Catalysts were prepared using a hydrothermal appro ...  NaF was added in the nanorod synthesis procedure.
1885,10.1016/j.electacta.2014.12.038,hydrothermal_ceramic_synthesis,α-Fe2O3 nanospheres were prepared under hydrotherm ...  400 degC for 5 h (heating rate was 5 degC min-1).
1886,10.1016/j.jcrysgro.2008.08.032,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.8 g Cu(CH3COO)2*4H2O was ... istilled water, and dried at 60 degC under vacuum."
1887,10.1016/j.jcis.2014.08.027,hydrothermal_ceramic_synthesis,All chemical reagents in our experiments were anal ... 270 degC for 2 h to obtain β-Bi2O3 hollow spheres.
1888,10.1016/j.matlet.2016.11.001,hydrothermal_ceramic_synthesis,Flower-like BaMoO4 was fabricated by the hydrother ... nol for several times and dried at 70 degC in air.
1889,10.1016/j.cej.2016.05.009,hydrothermal_ceramic_synthesis,1 mmol Bi(NO3)3*5H2O was dissolved into 10 mL ethy ...  where X wt% was the initial weight ratio of CQDs.
1890,10.1016/j.cej.2016.06.051,hydrothermal_ceramic_synthesis,"Two kinds of TiO2 nanostructures with different mo ... le was denoted as H-TiO2 and E-TiO2, respectively."
1891,10.1016/j.materresbull.2014.10.004,hydrothermal_ceramic_synthesis,"Typically, 1 mmol of Zn(OAc)2*2H2O and 2 mmol of F ... ol and dried in a vacuum oven at 60 degC for 12 h."
1892,10.1016/j.jssc.2010.08.004,hydrothermal_ceramic_synthesis,"In a typical procedure for fabrication of NiTe2 na ... everal times, and then dried at 60 degC in vacuum."
1893,10.1016/j.matlet.2013.12.068,hydrothermal_ceramic_synthesis,"At room temperature, CTAB (0.1 g) and NaOH (0.08 g ... usly under the same conditions as described above."
1894,10.1016/j.jcrysgro.2011.05.030,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.138 g (0.5 mmol) of FeCl ... ely, and finally dried in air at room temperature."
1895,10.1016/j.cej.2012.10.059,hydrothermal_ceramic_synthesis,"In a typical synthesis, 2 mmol of Ni(NO3)2[?]6H2O  ... een powder is annealed in air at 350 degC for 2 h."
1896,10.1016/j.jpcs.2011.02.004,hydrothermal_ceramic_synthesis,All the chemical reagents (analytical grade) were  ... at 353 K for 10 h before further characterization.
1897,10.1016/j.matlet.2016.03.042,hydrothermal_ceramic_synthesis,"In a typical hydrothermal procedure, 0.582 g (2 mm ...  degC min-1 and then calcined at 500 degC for 3 h."
1898,10.1002/chem.201200086,hydrothermal_ceramic_synthesis,Materials preparation: Mesoporous NiO nanowires we ... ursor materials were annealed at 400 degC for 2 h.
1899,10.1016/j.colsurfa.2010.04.028,hydrothermal_ceramic_synthesis,In a typical procedure of preparing Eu3+-doped Ba- ...  investigate controllable morphologies of the NCs.
1900,10.1016/j.electacta.2012.08.090,hydrothermal_ceramic_synthesis,All of the purchased reagents were analytical grad ... onstant except that 0.22 g l-lysine was not added.
1901,10.1016/j.matlet.2015.02.053,hydrothermal_ceramic_synthesis,All of the chemical reagents were analytic grade a ... t 80 degr for 7 h to obtain the white ZHS product.
1902,10.1016/j.electacta.2013.03.195,hydrothermal_ceramic_synthesis,The MoO2 nanoparticles were synthesized via a one- ... protection to obtain the final MoO2 nanoparticles.
1903,10.1016/j.matchemphys.2015.10.043,hydrothermal_ceramic_synthesis,All chemical reagents were of analytic purity and  ... products were dried in vacuum at 60 degC for 12 h.
1904,10.1016/j.ssi.2012.11.008,hydrothermal_ceramic_synthesis,"All the chemicals were of analytical purity and us ... roducts, named S-4h, S-6h, and S-8h, respectively."
1905,10.1016/j.apsusc.2010.12.135,hydrothermal_ceramic_synthesis,"A solution of Zn(AC)2 (2 mmol) in EtOH/H2O solvent ... nal products, and finally dried at 60 degC in air."
1906,10.1016/j.snb.2012.10.127,hydrothermal_ceramic_synthesis,"In a typical experiment, first, 2 mmol SnSO4 was d ... m at 60 degC for 5 h for further characterization."
1907,10.1016/j.matlet.2016.02.052,hydrothermal_ceramic_synthesis,"In a typical hydrothermal procedure, 0.582 g (2 mm ...  degC min-1 and then calcined at 400 degC for 2 h."
1908,10.1016/j.jssc.2015.11.032,hydrothermal_ceramic_synthesis,A typical hydrothermal synthesis procedure is desc ...  The experimental conditions are shown in Table 1.
1909,10.1016/j.matchemphys.2015.11.011,hydrothermal_ceramic_synthesis,All chemicals in the experiment were analytical gr ... for 20 min in air and black Co3O4 can be obtained.
1910,10.1016/j.jpowsour.2015.11.003,hydrothermal_ceramic_synthesis,All chemicals used in this study were in analytica ... r for 3 h to convert into the crystalline NiCo2O4.
1911,10.1016/j.mseb.2010.11.009,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade except β-CD ... 2 h and yellow CeO2 powders were obtained finally.
1912,10.1002/ejic.201100151,hydrothermal_ceramic_synthesis,"Synthesis: The chemicals Ti(OBu)4 (TNB, analytical ...  for three times, and drying at 80 degC overnight."
1913,10.1016/j.apcatb.2015.04.013,hydrothermal_ceramic_synthesis,The novel 3D BiOCl hierarchical architectures were ... r the same condition was prepared as a comparison.
1914,10.1016/j.matlet.2012.07.014,hydrothermal_ceramic_synthesis,"All chemical reagents were of analytic purity and  ... , and finally dried in vacuum at 60 degC for 10 h."
1915,10.1016/j.jcis.2016.07.037,hydrothermal_ceramic_synthesis,"All the reagents were of analytical grade and used ... es, and then dried in an oven at 60 degC for 24 h."
1916,10.1016/j.matlet.2015.08.049,hydrothermal_ceramic_synthesis,"In a typical process, 3 mmol of sodium molybdate a ... degC for 2 h in the tube furnace in N2 atmosphere."
1917,10.1016/j.jssc.2010.11.015,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade and were us ... quence, and then dried in air at 70 degC for 12 h."
1918,10.1016/j.actamat.2016.04.050,hydrothermal_ceramic_synthesis,"In a typical synthesis of Cu2-xSe nanostructures [ ... imes, and then dried at 60 degC for at least 12 h."
1919,10.1016/j.jpcs.2011.08.028,hydrothermal_ceramic_synthesis,All reagents were purchased from Shanghai Chemical ... ly changing the volume ratio of water and ethanol.
1920,10.1016/j.jpowsour.2011.08.085,hydrothermal_ceramic_synthesis,"All the chemicals were analytical grade without fu ... nal products, and finally dried at 60 degC in air."
1921,10.1016/j.apcatb.2016.04.009,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.55 g (1.66 mmol) Na2WO4  ... eral times, followed by drying at 60 degC for 6 h."
1922,10.1016/j.jmmm.2014.02.092,hydrothermal_ceramic_synthesis,Fe3O4 microplates were prepared by a facile hydrot ... and then were dried in vacuum at 60 degC for 12 h.
1923,10.1016/j.solmat.2010.10.008,hydrothermal_ceramic_synthesis,The VO2 nanorods were synthesized by a hydrotherma ... hanol several times and dried at 60 degC for 10 h.
1924,10.1002/smll.201601959,hydrothermal_ceramic_synthesis,"Preparation of α-MnO2 Nanorods: α-MnO2 nanorods we ... . Then, the sample was dried at 60 degC overnight."
1925,10.1016/j.materresbull.2012.12.059,hydrothermal_ceramic_synthesis,DWCNT-TiO2 hybrid was prepared by the hydrothermal ... m room temperature to 400 degC and holded for 2 h.
1926,10.1016/j.jhazmat.2010.08.096,hydrothermal_ceramic_synthesis,The typical preparation procedure of MgFe2O4 nanos ...  h. The sample was labeled as MgFe2O4 nanospheres.
1927,10.1016/j.physe.2007.11.024,hydrothermal_ceramic_synthesis,"All chemicals were reagent grade and used without  ... times, respectively, and dried at 50 degC for 8 h."
1928,10.1016/j.jssc.2003.09.010,hydrothermal_ceramic_synthesis,In the typical preparation of hexagonal NdPO4 nano ...  monoclinic NdPO4 was prepared at 220degC for 3 h.
1929,10.1002/asia.201403085,hydrothermal_ceramic_synthesis,"The CeVO4 nanobelts were synthesized through a hyd ... anol, and finally dried at 40 degC for 1 h in air."
1930,10.1016/j.jssc.2010.09.002,hydrothermal_ceramic_synthesis,"A series of Gd(OH)3:Eu3+ nanospheres were prepared ... ree times with ethanol, then air-dried at 60 degC."
1931,10.1016/j.jelechem.2016.03.009,hydrothermal_ceramic_synthesis,The SnS nanoparticles were synthesized according t ... d then dried in a vacuum oven at 65 degC for 24 h.
1932,10.1016/j.mseb.2015.11.001,hydrothermal_ceramic_synthesis,"ZnS nanorod was synthesized by simple one step sol ... by drying at 60 degC, a white powder was obtained."
1933,10.1016/j.matlet.2011.08.011,hydrothermal_ceramic_synthesis,All the reagents were of analytical grade and used ... ning the ZHC precursor at 300 degC for 2 h in air.
1934,10.1016/j.mssp.2014.08.045,hydrothermal_ceramic_synthesis,GO was prepared from natural flake graphite powder ... a parallel process without the introduction of GO.
1935,10.1016/j.jpowsour.2016.04.059,hydrothermal_ceramic_synthesis,In a typical procedure to prepare 2-nm C@PbMoO4 na ...  water (~5 mL) and stored for their posterior use.
1936,10.1016/j.cattod.2016.05.042,hydrothermal_ceramic_synthesis,"Core-shell structured CdS@TiO2 was synthesized acc ... zed water, and dried in vacuum at 70 degC for 5 h."
1937,10.1002/ejic.201001284,hydrothermal_ceramic_synthesis,Synthesis: Iron chloride (FeCl2 Guangdong Guanghua ... k samples were dried in vacuo at room temperature.
1938,10.1016/j.matlet.2005.05.076,hydrothermal_ceramic_synthesis,"All the chemicals used in the experiment were of a ... nal products, and finally dried at 60 degC in air."
1939,10.1016/j.cej.2016.04.128,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.5 g of Na2WO4*2H2O and 0 ... ight and then annealed in air at 500 degC for 2 h."
1940,10.1016/j.matlet.2015.01.043,hydrothermal_ceramic_synthesis,Synthesis of BiVO4: In a typical synthetic procedu ... nd then dried in vacuum at about 60 degC for 10 h.
1941,10.1016/j.apcatb.2010.04.023,hydrothermal_ceramic_synthesis,NaxH2-xTi3O7 NBs were synthesized with a hydrother ... s) was then dried at 60 degC in air for later use.
1942,10.1007/s10854-013-1373-1,hydrothermal_ceramic_synthesis,All the chemical reagents used were of analytical  ... od described above without adding In(NO3)3*4.5H2O.
1943,10.1016/j.matchemphys.2011.10.007,hydrothermal_ceramic_synthesis,"All chemicals were analytical grade and directly u ...  alcohol several times, dried at 80 degC for 24 h."
1944,10.1016/j.cej.2015.01.099,hydrothermal_ceramic_synthesis,"Pure TNTs (denoted as T-0) were synthesized by the ... alcined at 500 degC for 2 h (i.e., calcined TNTs)."
1945,10.1016/j.jallcom.2016.02.246,hydrothermal_ceramic_synthesis,"BiFeO3 nanostructures were synthesized by a simple ... times, respectively, and dried at 80 degC for 2 h."
1946,10.1002/cctc.201200840,hydrothermal_ceramic_synthesis,Nanoplate synthesis in the CH3COOK system: At RT ( ...  for 12 h. The final product was labelled as Fe-P.
1947,10.1016/j.matlet.2016.11.114,hydrothermal_ceramic_synthesis,All chemicals were purchased from Fisher Scientifi ... were then dried at 60 degC for 12 h and collected.
1948,10.1016/j.matlet.2013.01.104,hydrothermal_ceramic_synthesis,"In a typical preparing process, 20 mL of (NH4)2C2O ...  degC for 1 h in air to obtain the final products."
1949,10.1016/j.matlet.2010.08.062,hydrothermal_ceramic_synthesis,"All chemicals were directly used without further p ...  alcohol several times, dried at 80 degC for 24 h."
1950,10.1016/j.solidstatesciences.2009.06.010,hydrothermal_ceramic_synthesis,"In a typical procedure (hydrothermal method), 15 m ... ed white powders were dried at 90 degC in an oven."
1951,10.1016/j.matlet.2014.05.162,hydrothermal_ceramic_synthesis,"Synthesis of porous MoS2: The hydrothermal process ... , and drying in a vacuum oven at 40 degC for 24 h."
1952,10.1016/j.jallcom.2010.09.010,hydrothermal_ceramic_synthesis,"In a typical procedure, Bi(NO3)3*5H2O (5 mmol) was ... , and finally dried at 80 degC for 6 h in the air."
1953,10.1016/j.matlet.2013.01.020,hydrothermal_ceramic_synthesis,A typical synthesis of PbSe nanorods using a simpl ...  at 60 degC for 6 h for further characterizations.
1954,10.1016/j.apcatb.2011.10.008,hydrothermal_ceramic_synthesis,The pure BiOI samples were synthesized by a hydrot ... . The powders were collected as the final product.
1955,10.1016/j.snb.2013.05.029,hydrothermal_ceramic_synthesis,"All the reagents (analytical-grade purity) were us ... ure, urchin-like In2O3 microspheres were obtained."
1956,10.1016/j.matlet.2014.11.106,hydrothermal_ceramic_synthesis,"Multimorphologies nano-ZnO was synthesized from zi ...  degC for 60 min, at a heating rate of 1 degC/min."
1957,10.1016/j.electacta.2015.06.044,hydrothermal_ceramic_synthesis,The WO3 mesoscopic microspheres were synthesized u ... t time durations and with varying volumes of H2O2.
1958,10.1016/j.jmmm.2009.05.049,hydrothermal_ceramic_synthesis,All reagents were of analytical grade and used as  ... l product was dried in vacuum at 60 degC for 12 h.
1959,10.1016/j.biomaterials.2015.08.038,hydrothermal_ceramic_synthesis,Hydrophobic BaHoF5 NPs were synthesized through hy ...  NPs were obtained and redispersed in cyclohexane.
1960,10.1016/j.materresbull.2012.04.015,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.91 g (5 mmol) of V2O5 po ...  degC for future characterization and application."
1961,10.1016/j.jcis.2014.06.003,hydrothermal_ceramic_synthesis,"Magnetic MnFe2O4 nanoparticles were prepared by so ... , and then dried under vacuum at 60 degC for 12 h."
1962,10.1016/j.mseb.2015.12.003,hydrothermal_ceramic_synthesis,"SbCl3 (2 mmol) and Na2MoO4*2H2O (1 mmol) were in t ... s, and then dried under vacuum at 60 degC for 6 h."
1963,10.1016/j.matlet.2017.01.113,hydrothermal_ceramic_synthesis,To fabricate NiCo2O4 NNAs@ZnWO4 NFs coaxial struct ... egC for 2 h to obtain NiCo2O4 NNAs@ZnWO4 NFs (S2).
1964,10.1016/j.cplett.2007.07.082,hydrothermal_ceramic_synthesis,"NH4VO3 (2 mmol) was dissolved in hot distilled H2O ... ), and then dried under vacuum at 60 degC for 6 h."
1965,10.1016/j.matlet.2015.02.020,hydrothermal_ceramic_synthesis,All chemical reagents were of analytic purity and  ...  and dried in vacuum at 60 degC for more than 4 h.
1966,10.1016/j.apcatb.2016.07.025,hydrothermal_ceramic_synthesis,"Hydrothermal MoS2 was prepared by a previously rep ... ater and ethanol, and dried at 60 degC about 12 h."
1967,10.1016/j.materresbull.2016.04.018,hydrothermal_ceramic_synthesis,"TiOF2 nanocubes were synthesized through a hydroth ... s, and then dried at 60 degC for 12 h in a vacuum."
1968,10.1016/j.bios.2013.11.044,hydrothermal_ceramic_synthesis,MnCo2O4 NRs were synthesized using a simple templa ... ecipitate was calcined at 400 degC in air for 2 h.
1969,10.1016/j.cattod.2015.04.005,hydrothermal_ceramic_synthesis,The modified BiVO4 samples were prepared by a hydr ... d at 100 degC for 6 h to generate BiVO4 catalysts.
1970,10.1016/j.matlet.2010.10.019,hydrothermal_ceramic_synthesis,All chemicals used in this experiment were analyti ... products and dried in a vacuum at 60 degC for 4 h.
1971,10.1016/j.matlet.2011.07.033,hydrothermal_ceramic_synthesis,All chemical reagents were of analytic purity and  ... products were dried in vacuum at 80 degC for 10 h.
1972,10.1016/j.colsurfa.2012.03.052,hydrothermal_ceramic_synthesis,"As a comparison, hematite (α-Fe2O3) nanotubes were ... c air for 3 h with a heating rate of 1 degC min-1."
1973,10.1016/j.matlet.2007.05.030,hydrothermal_ceramic_synthesis,"In a typical procedure, NiCl2*6H2O (3 mmol) and he ... rities, and dried under vacuum at 60 degC for 4 h."
1974,10.1016/j.electacta.2013.09.171,hydrothermal_ceramic_synthesis,"In brief, 5 g glucose was dissolved in 30 mL deion ... ure without using ethanol (40 mL deionized water)."
1975,10.1016/j.matlet.2015.10.032,hydrothermal_ceramic_synthesis,All chemicals used were analytic grade reagents wi ... ned by annealing in a furnace at 550 degC for 2 h.
1976,10.1016/j.electacta.2012.08.008,hydrothermal_ceramic_synthesis,"SnO2 with high index facet (HIF SnO2) was synthesi ... der vacuum for 12 h, which is denoted as HIF SnO2."
1977,10.1016/j.electacta.2013.09.103,hydrothermal_ceramic_synthesis,Fe2O3/graphene composite was fabricated by a one-p ... similar method except for the absence of graphene.
1978,10.1016/j.apsusc.2012.12.027,hydrothermal_ceramic_synthesis,"Titania nanotubes (TiNT) were prepared by a hydrot ... rameters, we obtained high quality TiO2 nanotubes."
1979,10.1016/j.matlet.2008.10.019,hydrothermal_ceramic_synthesis,"In a typical procedure, 1.4 mmol NiSO4*6H2O, 1.4 m ...  followed by drying in an oven at 60 degC for 6 h."
1980,10.1016/j.apsusc.2012.12.078,hydrothermal_ceramic_synthesis,All chemicals were reagent grade and used without  ... dried in a vacuum drying box at 80 degC overnight.
1981,10.1016/j.jpowsour.2014.09.176,hydrothermal_ceramic_synthesis,In a typical process for synthesis of SnO2 nanoflo ... oducts were dried at 60 degC for 4 h under vacuum.
1982,10.1016/j.optmat.2015.07.030,hydrothermal_ceramic_synthesis,All reagents used for synthesis were purchased fro ...  ground in an agate mortar to obtain fine powders.
1983,10.1016/j.mseb.2010.03.088,hydrothermal_ceramic_synthesis,A series of NixZn1-xFe2O4 microspheres could be sy ... l product was dried in vacuum at 60 degC for 12 h.
1984,10.1016/j.matlet.2015.06.098,hydrothermal_ceramic_synthesis,"A typical synthesis procedure of the porous Cu2O d ... ethanol, and dried at 80 degC in a vacuum for 6 h."
1985,10.1016/j.jpowsour.2016.02.048,hydrothermal_ceramic_synthesis,"In the synthesis, 0.125 g CuSO4*5H2O is dissolved  ... nd then dried in a vacuum oven at 50 degC for 8 h."
1986,10.1016/j.ssi.2014.11.022,hydrothermal_ceramic_synthesis,All chemical reagents in this work were analytical ...  then dried in a vacuum oven at 60 degC overnight.
1987,10.1002/cnma.201600234,hydrothermal_ceramic_synthesis,The hydrothermal method was employed to synthesize ... l times with ethanol and dried at 60 degC for 6 h.
1988,10.1016/j.optmat.2011.12.010,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade and were us ... quence, and then dried in air at 70 degC for 12 h."
1989,10.1016/j.matlet.2008.11.017,hydrothermal_ceramic_synthesis,"In a typical procedure, 2 mmol CoCl2*6H2O and 2 mm ... thanol, then dried in a vacuum at 60 degC for 5 h."
1990,10.1002/chem.201405821,hydrothermal_ceramic_synthesis,"In a typical synthesis process, CoCl2[?]6H2O (294. ... s and drying in a vacuum oven at 60 degC for 12 h."
1991,10.1016/j.matlet.2014.08.053,hydrothermal_ceramic_synthesis,Synthesis of NiS hollow sphere: A typical synthesi ... ct was dried in a vacuum oven at 60 degC for 12 h.
1992,10.1016/j.matlet.2009.05.035,hydrothermal_ceramic_synthesis,All the chemicals were analytic grade reagents wit ... ethanol several times and dried in air at 60 degC.
1993,10.1016/j.mssp.2012.12.029,hydrothermal_ceramic_synthesis,All reagents were of analytical grade and used wit ... nd 24 h) were also obtained using the same method.
1994,10.1007/s00339-015-9461-0,hydrothermal_ceramic_synthesis,All reagents were of analytical grade from Shangha ... at 60 degC for 12 h to obtain the MoS2 nanosheets.
1995,10.1016/j.aca.2009.11.040,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.9 g of urea, 1 g of FeCl ... degC for 3 h in air and in nitrogen, respectively."
1996,10.1016/j.matlet.2009.01.054,hydrothermal_ceramic_synthesis,"In a typical hydrothermal process [24], 0.545 g zi ... sibly in the end product and finally dried in air."
1997,10.1016/j.electacta.2012.10.066,hydrothermal_ceramic_synthesis,The TiO2-B NBs were obtained according to our prev ... followed by autoclaving for 12 h at 200 degC [28].
1998,10.1007/s10853-009-3667-5,hydrothermal_ceramic_synthesis,All chemicals used in this experiment were analyti ... ts were dried in a vacuum oven at 40 degC for 6 h.
1999,10.1007/s10854-012-0634-8,hydrothermal_ceramic_synthesis,"In a typical synthesis, 12 mL of aqueous solution  ... ed at 500 degC for 2 h to obtain NiO microspheres."
2000,10.1016/j.jallcom.2015.10.117,hydrothermal_ceramic_synthesis,The hierarchical ZnO nanostructures were obtained  ... lcination at 500 degC in a muffle furnace for 4 h.
2001,10.1016/j.matlet.2014.03.110,hydrothermal_ceramic_synthesis,Synthesis of VS2nanoflowers: The VS2 nanoflowers w ... llowed by drying at 80 degC for 10 h under vacuum.
2002,10.1016/j.jcrysgro.2004.05.016,hydrothermal_ceramic_synthesis,"In a typical procedure, 1 mmol analytical-grade Sb ... d finally dried in a vacuum box at 50degC for 6 h."
2003,10.1016/j.matlet.2011.08.092,hydrothermal_ceramic_synthesis,"The experimental procedure was designed as follows ... l, and finally dried at 80 degC for 4 h in vacuum."
2004,10.1016/j.matlet.2010.01.067,hydrothermal_ceramic_synthesis,"Fe-Co binary ferrospinel (CoFe2O4) nanospheres wer ...  water and ethanol, and dried at 60 degC for 12 h."
2005,10.1016/j.cplett.2006.08.041,hydrothermal_ceramic_synthesis,"All chemical reagents in this experiment were of a ... al times, and dried at vacuum conditions for 24 h."
2006,10.1016/j.electacta.2013.05.085,hydrothermal_ceramic_synthesis,α-Fe2O3 was prepared by a hydrothermal method. 1.5 ... llowed by drying at 60 degC for 10 h under vacuum.
2007,10.1016/j.jallcom.2008.09.096,hydrothermal_ceramic_synthesis,"All chemical reagents were of analytical grade. In ... times, then dried under vacuum at 60 degC for 4 h."
2008,10.1016/j.cej.2016.02.065,hydrothermal_ceramic_synthesis,"The 2, 4-dihydroxybenzoic acid-formaldehyde (RF) m ... nd ethanol for several times and dried at 60 degC."
2009,10.1016/j.jpcs.2007.09.024,hydrothermal_ceramic_synthesis,"All chemicals used in this study were reagent-grad ...  400, 500, 600 and 800 degC for 4 h, respectively."
2010,10.1016/j.materresbull.2014.09.046,hydrothermal_ceramic_synthesis,All the chemical reagents were obtained from Beiji ... 0 degC for 2 h in air to yield yellow V2O5 powder.
2011,10.1016/j.matlet.2014.03.072,hydrothermal_ceramic_synthesis,The typical procedure is described as follows: 0.0 ... s with different doping levels were also obtained.
2012,10.1016/j.jallcom.2012.09.061,hydrothermal_ceramic_synthesis,"A typical synthetic procedure was as follows: SbCl ... ree times and ethanol once, then dried at 60 degC."
2013,10.1016/j.matchemphys.2013.03.066,hydrothermal_ceramic_synthesis,"All reagents were analytically pure, purchased fro ... ost treatment process is the same as that of BiOI."
2014,10.1016/j.jallcom.2012.08.124,hydrothermal_ceramic_synthesis,The source material of the W18O49 nanorods was syn ... er and ethanol and then dried at 60 degC for 12 h.
2015,10.1016/j.electacta.2016.06.144,hydrothermal_ceramic_synthesis,H2Ti12O25 nanorods was prepared by hydrothermal me ... h in air in sequence to obtain H2Ti12O25 nanorods.
2016,10.1016/j.jcis.2011.02.052,hydrothermal_ceramic_synthesis,All reagents are analytically pure and used as-rec ... C for 4 h before characterization and application.
2017,10.1016/j.snb.2014.02.057,hydrothermal_ceramic_synthesis,Nickel hydroxide nanopetals were synthesized by a  ... illed water and then dried at ambient temperature.
2018,10.1016/j.electacta.2012.11.089,hydrothermal_ceramic_synthesis,"All the chemicals used in this experiment were of  ... lute ethanol, and dried at 60 degC for 8 h in air."
2019,10.1016/j.nanoen.2014.04.005,hydrothermal_ceramic_synthesis,Synthesis of Li2Mn0.5Fe0.5SiO4at a low temperature ... 0 degC overnight. This sample was named as LMFS-2.
2020,10.1002/jctb.2256,hydrothermal_ceramic_synthesis,"α-MnO2 was prepared through a low-temperature liqu ... ts, and finally dried at 60 degC as α-MnO2 powder."
2021,10.1016/j.jssc.2014.07.024,hydrothermal_ceramic_synthesis,All the chemicals were purchased from Shanghai Che ... everal times and finally dried at 60 degC for 8 h.
2022,10.1007/s10800-016-0985-6,hydrothermal_ceramic_synthesis,MnCO3 was synthesized via hydrothermal method by u ... ace for 3 h to obtain the porous Mn2O3 microcubes.
2023,10.1016/j.elecom.2008.07.049,hydrothermal_ceramic_synthesis,"In a typical procedure, 10 mmol titanium tetraisop ... nally the powder was calcined at 500 degC for 2 h."
2024,10.1016/j.matlet.2011.11.052,hydrothermal_ceramic_synthesis,Fe3O4 submicrospheres were prepared via a modified ... dried at 60 degC overnight giving the black Fe3O4.
2025,10.1016/j.matlet.2009.10.050,hydrothermal_ceramic_synthesis,All reagents were commercial products with analyti ... finally dried in a vacuum oven at 60 degC for 4 h.
2026,10.1016/j.matlet.2011.05.064,hydrothermal_ceramic_synthesis,"All chemical reagents were of analytical grade and ... thanol, and dried under vacuum at 60 degC for 4 h."
2027,10.1016/j.ces.2016.01.018,hydrothermal_ceramic_synthesis,"The TiO2 nanotube (TiNT) was synthesized by a modi ... r 2 h to obtain TiO2 nanotube, designated as TiNT."
2028,10.1016/j.matlet.2015.11.112,hydrothermal_ceramic_synthesis,All chemicals used were analytic grade reagents wi ... ned by annealing in a furnace at 550 degC for 2 h.
2029,10.1007/s10854-014-2074-0,hydrothermal_ceramic_synthesis,All the reagents used in this experiment were purc ... ght. The obtained powder was named as flower-like.
2030,10.1016/j.optmat.2016.11.003,hydrothermal_ceramic_synthesis,"In this work, WS2 nanosheets were synthesized by a ... times, respectively, and dried at 60 degC for 6 h."
2031,10.1016/j.matlet.2015.09.010,hydrothermal_ceramic_synthesis,CF-SnO2 hierarchical nanosheets were synthesized b ...  the formation of SF-SnO2 hierarchical nanosheets.
2032,10.1016/j.cplett.2016.10.079,hydrothermal_ceramic_synthesis,"The NiO-Co3O4 composites were prepared by a facile ... th the ramping rate of 5 degC min-1, respectively."
2033,10.1016/j.electacta.2014.10.022,hydrothermal_ceramic_synthesis,The pure γ-Fe2O3 was prepared through a solvotherm ... trate precursor powder at 320 degC in air for 1 h.
2034,10.1016/j.jallcom.2012.10.105,hydrothermal_ceramic_synthesis,"Firstly, 10 mL 0.1 M Zn(CH3COO)2*2H2O (1 mmol) and ... s relatively high (84.9%) for hydrothermal method."
2035,10.1016/j.electacta.2014.08.088,hydrothermal_ceramic_synthesis,"The precursors, α-MnO2 with different morphologies ... lar process by the reported methods [23] and [24]."
2036,10.1016/j.electacta.2016.06.038,hydrothermal_ceramic_synthesis,"NiCl2*6H2O (0.47 g), MnCl2 (0.08 g), and HMT (0.46 ... r four times and dried at 60 degC for 8 h in oven."
2037,10.1007/s10854-013-1107-4,hydrothermal_ceramic_synthesis,Synthesis of nanospheres and nanoflowers: In a typ ... he same process except that citric acid was added.
2038,10.1016/j.matlet.2011.06.049,hydrothermal_ceramic_synthesis,"In the synthesis of SnO2/SnS2 nanocomposite, 3 mmo ...  ethanol, and dried in vacuum at 100 degC for 3 h."
2039,10.1016/j.jcrysgro.2003.09.027,hydrothermal_ceramic_synthesis,All chemicals (analytical grade reagents) were pur ...  then finally dried in a vacuum at 60degC for 6 h.
2040,10.1016/j.physe.2013.03.006,hydrothermal_ceramic_synthesis,All the reagents in this study were of analytical  ...  were set to illustrate the effects of EG and PEG.
2041,10.1002/crat.201300397,hydrothermal_ceramic_synthesis,ZnO/α-Fe2O3 nanocomposites were synthesized by a s ...  but without the addition of α-Fe2O3 nanospindles.
2042,10.1016/j.matlet.2007.12.032,hydrothermal_ceramic_synthesis,"In a typical experimental procedure, 80 ml solvent ... degC for 12 h, and black precipitate was obtained."
2043,10.1016/j.matchemphys.2013.04.018,hydrothermal_ceramic_synthesis,All chemical reagents were of analytical grade and ... NO3 and H2SO4 instead of HCl was also carried out.
2044,10.1002/cplu.201500534,hydrothermal_ceramic_synthesis,"Typically, different amounts of FMNFs were dispers ... s were synthesized by direct calcination of FMNFs."
2045,10.1016/j.electacta.2014.10.064,hydrothermal_ceramic_synthesis,0.225 mmol Ni (AC)2*4H2O and 0.45 mmol Co (AC)2*4H ... at 300 degC in air for 3 h to obtain the products.
2046,10.1007/s10854-016-5390-8,hydrothermal_ceramic_synthesis,The TiO2 nanowires (TiO2 NWs) were synthesized thr ... re obtained by heat treatment for 2 h at 600 degC.
2047,10.1016/j.matlet.2014.05.208,hydrothermal_ceramic_synthesis,"Synthesis of Samples. CoCl2*6H2O (2.38 g), CO(NH2) ... it was dried in a vacuum oven at 60 degC for 24 h."
2048,10.1016/j.powtec.2011.04.028,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade and used wi ... CuCl2*6H2O or reaction temperature were conducted.
2049,10.1016/j.apcatb.2015.03.042,hydrothermal_ceramic_synthesis,"The flower-like Bi2MoO6 spheres were prepared acco ...  80 degC in air, and calcined at 400 degC for 2 h."
2050,10.1016/j.matlet.2012.01.075,hydrothermal_ceramic_synthesis,"All chemicals were analytical grade reagent. In a  ... ated as ""In2O3-350"" and ""In2O3-400"", respectively."
2051,10.1016/j.jcis.2013.08.031,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.5 g of pvp (MW: 360, 000 ... e keeping the other synthetic conditions constant."
2052,10.1016/j.solidstatesciences.2011.10.019,hydrothermal_ceramic_synthesis,All chemical reagents purchased from Shanghai Chem ... cohol several times and dried at 80 degC for 10 h.
2053,10.1016/j.cej.2015.12.080,hydrothermal_ceramic_synthesis,"Bulk g-C3N4 was synthesized using a method reporte ...  water and ethanol, and dried at 70 degC for 10 h."
2054,10.1016/j.apsusc.2013.09.108,hydrothermal_ceramic_synthesis,"In a typical synthesis procedure, FeCl3*6H2O (2.5  ... hanol, and dried under vacuum at 60 degC for 10 h."
2055,10.1016/j.jcis.2011.01.076,hydrothermal_ceramic_synthesis,All reagents were purchased from Shanghai Chemical ... red sample was dried in vacuum at 60 degC for 6 h.
2056,10.1016/j.matlet.2014.01.173,hydrothermal_ceramic_synthesis,Synthesis of CuS microstructures. In a typical pro ...  for several times and dried in vacuum at 60 degC.
2057,10.1016/j.apsusc.2012.11.025,hydrothermal_ceramic_synthesis,"In a typical synthesis, 37.5 ml isopropyl was mixe ... imple hydrothermal method as reported before [18]."
2058,10.1016/j.electacta.2014.12.074,hydrothermal_ceramic_synthesis,The NiS nanoparticles were synthesized by a facile ... ter/ethanol and dried in air at 60 degC overnight.
2059,10.1016/j.ssc.2005.06.033,hydrothermal_ceramic_synthesis,"In a typical procedure, 2 mmol KMnO4 and 0.10-0.50 ... ral times, and dried at 60 degC for 4 h in vacuum."
2060,10.1016/j.matchemphys.2005.11.027,hydrothermal_ceramic_synthesis,"All chemical reagents were of analytical grade and ... times, then dried under vacuum at 60 degC for 4 h."
2061,10.1016/j.apcatb.2014.10.075,hydrothermal_ceramic_synthesis,"For the syntheses of Bi24O31Cl10 nanosheets, 0.004 ... y using the same procedure without adding NH3*H2O."
2062,10.1016/j.jssc.2009.01.042,hydrothermal_ceramic_synthesis,"All chemical reagents were of analytical grade. In ... s, and then dried under vacuum at 80 degC for 4 h."
2063,10.1016/j.apsusc.2012.05.075,hydrothermal_ceramic_synthesis,Subsequently MC/Bi2WO6 were prepared by hydrotherm ... hen dried at 80 degC for 6 h for characterization.
2064,10.1002/chem.201301563,hydrothermal_ceramic_synthesis,"Materials synthesis: In a typical synthesis proced ... oven, overnight, the final products were obtained."
2065,10.1016/j.matlet.2015.08.090,hydrothermal_ceramic_synthesis,"All chemicals (98% purity, analytical grade) were  ... ral times with DI water and ethanol, respectively."
2066,10.1016/j.ssi.2010.05.058,hydrothermal_ceramic_synthesis,"ZnO nanosheets were synthesized by a simple mixed  ... , the precipitates were dried at 60 degC for 10 h."
2067,10.1016/j.ssi.2010.06.027,hydrothermal_ceramic_synthesis,All the reagents are of analytical purity grade an ...  500 degC for 5 h at a heating rate of 5 degC/min.
2068,10.1016/j.matlet.2012.01.064,hydrothermal_ceramic_synthesis,All reagents of analytical grade were purchased fr ...  several times and then dried at 80 degC for 12 h.
2069,10.1016/j.electacta.2013.10.154,hydrothermal_ceramic_synthesis,"In a typical synthesis, 1 mmol of Ni(CH3COO)2*4H2O ... tain the hierarchical ultrathin NiMoO4 nanosheets."
2070,10.1016/j.cej.2016.04.068,hydrothermal_ceramic_synthesis,"All chemicals used in this work were analytical re ... or 8 h. Finally, the Cu-BTC material was obtained."
2071,10.1007/s10854-011-0443-5,hydrothermal_ceramic_synthesis,3 mL tetrabutyl titanate (Ti(OBu)4) was added into ... eral hours. The sample obtained was denoted by S1.
2072,10.1016/j.jallcom.2011.12.079,hydrothermal_ceramic_synthesis,"For the hydrothermal synthesis of LiMn2O4, 0.87 g  ... d then dried in a vacuum oven at 120 degC for 6 h."
2073,10.1016/j.electacta.2016.11.118,hydrothermal_ceramic_synthesis,"The synthesis of the NCS powders was basically fol ...  ethanol, and dried in vacuum at 100 degC for 2 h."
2074,10.1016/j.matlet.2013.05.067,hydrothermal_ceramic_synthesis,Preparation of mesoporous ZnS hollow spheres (MZHS ... stilled water and finally dried at 80 degC in air.
2075,10.1016/j.materresbull.2009.04.005,hydrothermal_ceramic_synthesis,"The monoclinic BiVO4 nanoribbons were synthesized  ... s, and finally dried in vacuum at 50 degC for 6 h."
2076,10.1016/j.materresbull.2015.02.024,hydrothermal_ceramic_synthesis,"The CdS/BiPO4 composites were synthesized through  ... O4 and were 0.3, 0.5, 0.8, 1.0, 1.5, respectively."
2077,10.1016/j.nanoen.2016.05.042,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade and were us ... everal times, and vacuum dried at 80 degC for 6 h."
2078,10.1016/j.solener.2011.12.006,hydrothermal_ceramic_synthesis,CdS nanoparticles were prepared by a hydrothermal  ... nol and then dried under vacuum at 368 K for 24 h.
2079,10.1016/j.matlet.2015.02.134,hydrothermal_ceramic_synthesis,"Synthesis of SnS2/La2Ti2O7nanoheterojunctions: 5 m ... ute ethanol, and dried in air at 80 degC for 12 h."
2080,10.1016/j.solidstatesciences.2014.02.003,hydrothermal_ceramic_synthesis,All the chemicals used in this experiment were of  ... . The powders were collected for characterization.
2081,10.1016/j.matlet.2009.12.036,hydrothermal_ceramic_synthesis,"0.154 g of FeSO4*6H2O, 0.07 g of CoCl2*6H2O, and 0 ... btained and characterized as Co/CoFe2O4 nanobelts."
2082,10.1007/s10854-012-0682-0,hydrothermal_ceramic_synthesis,"ZnO nanosheet-based hierarchical microarchitecture ... er and ethanol, and then dried at 90 degC for 5 h."
2083,10.1016/j.matlet.2015.01.097,hydrothermal_ceramic_synthesis,"Synthesis of Ag3PO4/ZnFe2O4: All the reagents used ...  distilled water, and then dried in a vacuum oven."
2084,10.1016/j.electacta.2013.06.060,hydrothermal_ceramic_synthesis,WS2-Gr composites were prepared by a modified l-cy ...  then dried in a vacuum oven at 353.15 K for 24 h.
2085,10.1016/j.electacta.2010.07.049,hydrothermal_ceramic_synthesis,Li3V2(PO4)3 nanorods have been prepared by hydroth ... ed at 80 degCC for at least 24 h in a vacuum oven.
2086,10.1016/j.electacta.2015.10.050,hydrothermal_ceramic_synthesis,"In a typical synthesis of CoS nanoparticles, 1.011 ... tant CoS powders were used without post-treatment."
2087,10.1016/j.apcatb.2015.10.052,hydrothermal_ceramic_synthesis,"CeVO4 nanorods were prepared by a simple hydrother ...  anhydrous ethanol, and dried at 80 degC for 12 h."
2088,10.1016/j.snb.2016.01.106,hydrothermal_ceramic_synthesis,In2O3 with different morphologies was prepared by  ... recipitates at 600 degC for 3 h in air atmosphere.
2089,10.1007/s10854-013-1267-2,hydrothermal_ceramic_synthesis,All reagents were analytic grade and used without  ... times and finally dried in vacuum oven at 75 degC.
2090,10.1016/j.carbpol.2016.03.076,hydrothermal_ceramic_synthesis,"The α-MnO2 nanorods were synthesized by a hydrothe ... n a vacuum oven, the final products were obtained."
2091,10.1007/s10854-014-1708-6,hydrothermal_ceramic_synthesis,"In a typical procedure, Fe3O4 nanocrystals were pr ... onized water, and dried in air for 4 h at 80 degC."
2092,10.1016/j.jpcs.2010.09.006,hydrothermal_ceramic_synthesis,"The precursor was prepared according to the proced ... 00 degC, and the red α-Fe2O3 product was obtained."
2093,10.1016/j.materresbull.2014.08.022,hydrothermal_ceramic_synthesis,SnO2 was synthesized based on the hydrothermal rou ...  and then was dried in vacuum at 60 degC for 12 h.
2094,10.1002/ep.12239,hydrothermal_ceramic_synthesis,MIL-101(Cr) using HF was prepared by the conventio ... 0degC for overnight and designated as MIL-101(HF).
2095,10.1016/j.matlet.2015.07.149,hydrothermal_ceramic_synthesis,TiO2{001} nanosheets were synthesized via a simple ... ions without the presence of TiO2{001} nanosheets.
2096,10.1016/j.jhazmat.2014.06.061,hydrothermal_ceramic_synthesis,TiO2 nanotube was fabricated by a previous reporte ... ealed at 450 degC for 2 h to obtain TiO2 nanotube.
2097,10.1016/j.matchar.2011.01.001,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.4 g of copper diethyldit ... l several times, and dried in a vacuum at 50 degC."
2098,10.1016/j.electacta.2013.12.015,hydrothermal_ceramic_synthesis,SnO2 was synthesized based on the hydrothermal rou ...  and then was dried in vacuum at 60 degC for 12 h.
2099,10.1016/j.jcis.2015.04.070,hydrothermal_ceramic_synthesis,"Firstly, 1.759 g Mn(Ac)2[?]4H2O and 2.307 g sodium ... move the SDBS, and then dried at 60 degC for 12 h."
2100,10.1016/j.jmmm.2015.04.009,hydrothermal_ceramic_synthesis,All chemicals were of analytic grade and used as r ... synthesis of nanospheres is illustrated in Fig. 1.
2101,10.1016/j.jpowsour.2009.07.056,hydrothermal_ceramic_synthesis,Sm(NO3)3*6H2O and Ce(NO3)3*6H2O raw materials were ...  hydrothermal synthesis are referred to as SDC-HT.
2102,10.1016/j.nanoen.2016.12.010,hydrothermal_ceramic_synthesis,The ZnSe[DETA]0.5 nanobelts were prepared by a mod ... obelts were dried at 80 degC for 6 h under vacuum.
2103,10.1016/j.jallcom.2009.03.043,hydrothermal_ceramic_synthesis,"All of the reactants were analytical grade, bought ... red sample was dried in vacuum at 60 degC for 6 h."
2104,10.1016/j.matlet.2007.12.041,hydrothermal_ceramic_synthesis,All chemicals are of analytical grade and were use ... er for several times and dried at 60 degC for 6 h.
2105,10.1016/j.jssc.2011.12.007,hydrothermal_ceramic_synthesis,"A mixture of Mel (0.342 g, 1.00 mmol), Eu(NO3)3*6H ... er (3x10 ml) and air dried at ambient temperature."
2106,10.1016/j.jssc.2012.07.054,hydrothermal_ceramic_synthesis,"1 was hydrothermally prepared by a mixture of Na9[ ...  (3): C 4.93 (4.80), H 1.63 (1.54), N 3.84 (3.98)."
2107,10.1016/j.electacta.2016.01.003,hydrothermal_ceramic_synthesis,Layered MoS2 was prepared by the method reported i ... btained by drying precipitate at 60 degC for 24 h.
2108,10.1016/j.solidstatesciences.2006.05.003,hydrothermal_ceramic_synthesis,"All chemical agents were analytical grade and used ... , and finally dried in vacuum at 50 degC for 12 h."
2109,10.1016/j.matdes.2016.04.043,hydrothermal_ceramic_synthesis,"Bi2S3 nanorods with orthorhombic structure were pr ...  three times, afterward, dried at 60 degC for 8 h."
2110,10.1016/j.solidstatesciences.2014.03.005,hydrothermal_ceramic_synthesis,All chemicals were analytical grade without furthe ...  dried at 80 degC to form pure SrTiO3 nano-powder.
2111,10.1016/j.jssc.2008.06.002,hydrothermal_ceramic_synthesis,"In total, 1.03 g (10 mmol) of the as-prepared GaOO ... finally dried in a vacuum oven at 60 degC for 8 h."
2112,10.1016/j.jpowsour.2011.10.132,hydrothermal_ceramic_synthesis,0.480 g l-cysteine (l-cys) was dissolved in 40 ml  ... e procedure without the presence of GO nanosheets.
2113,10.1016/j.materresbull.2012.11.070,hydrothermal_ceramic_synthesis,"CdxZn(1-x)S semiconductor alloys were prepared via ...  added CdCl2*2.5H2O at 2, 1, 0.5, 0.2, and 0 mmol."
2114,10.1016/j.matlet.2011.08.084,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.6706 g stannous sulfate  ...  2 h in air to obtain the pompon-like porous SnO2."
2115,10.1016/j.materresbull.2010.09.023,hydrothermal_ceramic_synthesis,"In a typical procedure, 35 mL K4[Fe(CN)6] aqueous  ... tical grade and used without further purification."
2116,10.1002/chem.200802182,hydrothermal_ceramic_synthesis,"All the reagents in the experiments were analytica ...  conducted, while other conditions kept unchanged."
2117,10.1016/j.cplett.2014.12.047,hydrothermal_ceramic_synthesis,"0.4830 g of Cu(NO3)2*3H2O was dissolved into 8 mL  ... ethanol, and then vacuum dried at 60 degC for 8 h."
2118,10.1016/j.jallcom.2014.11.137,hydrothermal_ceramic_synthesis,The synthesis of CuS with surfactant as additive w ... d then dried in a vacuum oven at 60 degC for 12 h.
2119,10.1016/j.ijhydene.2013.03.016,hydrothermal_ceramic_synthesis,"NaOH aqueous solution were spilled into an aqueous ... NaOH (nNaOH = 0, 0.02, 0.04, 0.06, 0.08, 0.1 mol)."
2120,10.1016/j.matlet.2013.05.143,hydrothermal_ceramic_synthesis,All the reagents in the experiment were analytical ... hierarchical α-Fe2O3 hollow spheres were obtained.
2121,10.1007/s11051-011-0240-3,hydrothermal_ceramic_synthesis,Titanate nanostructures were prepared as described ...  All samples were dried at 60 +- 10 degC for 24 h.
2122,10.1016/j.jcrysgro.2006.10.138,hydrothermal_ceramic_synthesis,All the reagents are of analytical grade from Shan ... ities and finally dried at 60 degC for 6 h in air.
2123,10.1016/j.electacta.2013.07.168,hydrothermal_ceramic_synthesis,"The MoS2 nanocomposite was synthesized as follows: ... mes, and then dried in vacuum at 60 degC for 24 h."
2124,10.1007/s10008-011-1620-4,hydrothermal_ceramic_synthesis,"In a typical procedure, an aqueous solution (10 mL ... onditions but without the presence of GO or FeCl3."
2125,10.1016/j.electacta.2007.10.020,hydrothermal_ceramic_synthesis,All the chemicals were of analytical purity and us ... at 200 degC for 3 h to obtain the desired product.
2126,10.1016/j.jhazmat.2015.06.012,hydrothermal_ceramic_synthesis,The different MnO2 samples were prepared according ... o washed with water and dried at 80 degC for 12 h.
2127,10.1016/j.matlet.2009.06.010,hydrothermal_ceramic_synthesis,All chemical reagents used in this work were of ch ... oducts. The final products were then dried in air.
2128,10.1007/s10854-015-3172-3,hydrothermal_ceramic_synthesis,"In a typical synthesis of γ-MnOOH nanotube, 8 mmol ... dried at 80 degC for subsequent characterizations."
2129,10.1016/j.jpowsour.2012.06.104,hydrothermal_ceramic_synthesis,All the chemicals studied in the experiments were  ... R-TiO2 obtained was used to prepare NR-TiO2 paste.
2130,10.1016/j.cplett.2003.09.037,hydrothermal_ceramic_synthesis,"The method of hydrothermal synthesis, as described ... for 2 h, finally a soft white powder was obtained."
2131,10.1002/adma.201104546,hydrothermal_ceramic_synthesis,Synthesis of Cu2O@TiO2 core/shell structures: 0.01 ... DI water and ethanol for further characterization.
2132,10.1016/j.carbon.2014.10.016,hydrothermal_ceramic_synthesis,The SnO2 nanoparticles were synthesized using a si ... d at 80 degC for 8 h to obtain SnO2 nanoparticles.
2133,10.1007/s10854-013-1286-z,hydrothermal_ceramic_synthesis,"In a typical experiment, 0.3 mmol of cadmium aceta ... water several times to remove residual impurities."
2134,10.1016/j.matlet.2012.03.023,hydrothermal_ceramic_synthesis,"All reagents were of analytical grade and used wit ... , and then dried in an oven overnight at 110 degC."
2135,10.1016/j.matdes.2016.09.098,hydrothermal_ceramic_synthesis,The hydrothermal method was adopted to prepare flo ... nO2 product would be dried at 70 degC in the oven.
2136,10.1016/j.cej.2015.09.012,hydrothermal_ceramic_synthesis,"The SBC@β-FeOOH was prepared by a hydrothermal rea ... , and finally dried under vacuum at 333 K for 6 h."
2137,10.1016/j.nanoen.2016.06.029,hydrothermal_ceramic_synthesis,"In a typical procedure, 2 mL Ti-isopropoxide and 2 ... dried product was then heated at 450 degC for 2 h."
2138,10.1016/j.apsusc.2010.03.123,hydrothermal_ceramic_synthesis,"ZnO nanorods were prepared by a SDS-assisted hydro ... t 60 degC for 3 h, and ZnO nanorods were obtained."
2139,10.1016/j.jpowsour.2014.09.048,hydrothermal_ceramic_synthesis,"In a typical procedure, NH4VO3 (0.77 g) and oxalic ...  to produce highly-crystallized V2O5 microflowers."
2140,10.1016/j.jssc.2007.01.017,hydrothermal_ceramic_synthesis,"All the reagents were analytical reagent grade, an ... he absence of CTAB, no any products were obtained."
2141,10.1016/j.materresbull.2015.03.041,hydrothermal_ceramic_synthesis,SnO2@G nanocomposite was prepared by a simple hydr ... d by the same method only without adding graphene.
2142,10.1016/j.cplett.2011.06.033,hydrothermal_ceramic_synthesis,TiO2 nanoparticles were prepared as follows. In a  ... anoparticles were examined by electron microscopy.
2143,10.1016/j.cplett.2005.09.138,hydrothermal_ceramic_synthesis,"All the analytical chemicals were purchased from S ... al times, and dried in vacuum at 50 degC for 12 h."
2144,10.1016/j.apcatb.2015.04.022,hydrothermal_ceramic_synthesis,"In a typical procedure, 6 mmol Na2SO4 and 2 mmol B ... tuning the molar ratio of Na2SO4 to Bi(NO3)3*5H2O."
2145,10.1016/j.jcrysgro.2006.06.002,hydrothermal_ceramic_synthesis,For the solvothermal synthesis of the ZnO crystals ... cessively and dried in vacuum at room temperature.
2146,10.1016/j.micromeso.2007.10.034,hydrothermal_ceramic_synthesis,"All the chemicals were of analytical grade and wer ... , washed and dried in a vacuum at 50 degC for 4 h."
2147,10.1016/j.electacta.2015.12.127,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade and used wi ... lled water several times to obtain the final SnS2.
2148,10.1007/s11837-014-0983-2,hydrothermal_ceramic_synthesis,A total of 2.5 mmol of Co(NO3)2*6H2O was dissolved ... xagonal Co3O4 nanosheets were synthesized (as S6).
2149,10.1016/j.electacta.2012.09.003,hydrothermal_ceramic_synthesis,All the concerned regents are of analytic grade an ... ely and dried in oven at 100 degC for further use.
2150,10.1016/j.matlet.2012.04.004,hydrothermal_ceramic_synthesis,"The procedure used to prepare YVO4:Yb3+,Er3+ powde ... for several times, and dried at 120 degC for 10 h."
2151,10.1016/j.electacta.2014.10.079,hydrothermal_ceramic_synthesis,"The synthesis of CuS nanosheets were as follows: 1 ... l times, and dried in vacuum at 80 degC overnight."
2152,10.1016/j.apcatb.2017.01.049,hydrothermal_ceramic_synthesis,CDs were prepared via an electrochemical etching m ... synthesized under the same conditions without CDs.
2153,10.1016/j.matlet.2008.02.065,hydrothermal_ceramic_synthesis,The experimental procedure was designed as follows ... rsed in the absolute ethanol for characterization.
2154,10.1016/j.apcatb.2015.04.022,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.67 mmol Na2SO4 and 2 mmo ...  degC in air. The product yields was about 0.64 g."
2155,10.1007/s10008-015-2739-5,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade and were us ... by structural and morphological characterizations.
2156,10.1016/j.ces.2015.03.060,hydrothermal_ceramic_synthesis,The δ-Bi2O3 samples were prepared according to the ... illed water and finally dried at 70 degC for 10 h.
2157,10.1016/j.powtec.2012.12.051,hydrothermal_ceramic_synthesis,"5.0 mmol SnCl4*5H2O and an appropriate amount of Z ... ed water, and dried in vacuum at 100 degC for 3 h."
2158,10.1016/j.cej.2014.01.070,hydrothermal_ceramic_synthesis,α-MoO3 nanowires are synthesized via a hydrotherma ... spension containing α-MoO3 nanowires was obtained.
2159,10.1016/j.actamat.2013.11.076,hydrothermal_ceramic_synthesis,"All chemicals were analytical grade and were used  ... three times each, then dried at 60 degC overnight."
2160,10.1016/j.powtec.2012.03.019,hydrothermal_ceramic_synthesis,"In a typical process, 3.16 g KMnO4 and 5.07 g MnSO ... l black powder was collected for characterization."
2161,10.1016/j.ssc.2008.09.058,hydrothermal_ceramic_synthesis,1D composite structures were synthesized by hydrot ... xperimental parameters were summarized in Table 1.
2162,10.1007/s11837-013-0607-2,hydrothermal_ceramic_synthesis,"In first category, 2 mmol of NH4Fe(SO4)2*12H2O and ... e one with cyclohexylamine was abbreviated as S-2."
2163,10.1016/j.jssc.2010.04.008,hydrothermal_ceramic_synthesis,"Sr(NO3)2 (9 mmol), Al(NO3)3*9H2O (6 mmol), CO(NH2) ... s, and then dried under vacuum at 60 degC for 6 h."
2164,10.1016/j.jallcom.2010.05.169,hydrothermal_ceramic_synthesis,All chemicals used in the experiment were of analy ... nd finally dried under vacuum at 60 degC for 10 h.
2165,10.1016/j.apsusc.2016.08.031,hydrothermal_ceramic_synthesis,The schematic illustration of MoS2 layer synthesis ... and then dried in vacuum at 45 degC for overnight.
2166,10.1016/j.snb.2012.05.054,hydrothermal_ceramic_synthesis,"0.035 g of α-MoO3 nanorods obtained above was disp ... ute ethanol, and dried at 80 degC for 12 h in air."
2167,10.1016/j.colsurfa.2011.09.056,hydrothermal_ceramic_synthesis,"To synthesize β-MnO2 nanowires, a modified hydroth ...  product, followed by drying at 105 degC for 24 h."
2168,10.1007/s10800-014-0779-7,hydrothermal_ceramic_synthesis,CuO microspheres were synthesized by hydrothermal  ... f PVP. The obtained CuO sample was denoted as CuO.
2169,10.1016/j.matlet.2013.11.089,hydrothermal_ceramic_synthesis,Preparation of MnO2: The synthesis procedure under ... ith distilled water and dried at 60 degC for 12 h.
2170,10.1016/j.jallcom.2015.10.212,hydrothermal_ceramic_synthesis,SnO2 and SnO2/C composite were synthesized using a ... for comparison. The reactions can be expressed as:
2171,10.1016/j.apsusc.2011.07.116,hydrothermal_ceramic_synthesis,"Shuttle-like ZnO nano/microrods were synthesized v ...  water and ethanol, and dried at 80 degC for 12 h."
2172,10.1016/j.electacta.2009.02.060,hydrothermal_ceramic_synthesis,"All the chemicals were of analytical purity and us ... ucts, named S-300, S-450, and S-600, respectively."
2173,10.1016/j.apcatb.2015.03.001,hydrothermal_ceramic_synthesis,"The 3D hierarchical BiOCl microflowers were prepar ... r and ethanol several times, and dried at 70 degC."
2174,10.1002/asia.201402319,hydrothermal_ceramic_synthesis,"The SMIOs were synthesized by using a modified sol ... ionized water several times, and dried at 60 degC."
2175,10.1016/j.jssc.2011.11.031,hydrothermal_ceramic_synthesis,"All reagents were of analytical grade without furt ... 6 h in air to obtain In2O3, and named as Sample 1."
2176,10.1016/j.jssc.2011.12.010,hydrothermal_ceramic_synthesis,"In a typical synthesis, 3 mmol AgNO3, 3 mmol Bi(NO ... e preparation is systematically shown in Scheme 1."
2177,10.1007/s10854-015-3476-3,hydrothermal_ceramic_synthesis,"All chemicals used in this work were of analytic p ... al times, then dried in vacuum at 80 degC for 4 h."
2178,10.1016/j.matlet.2015.09.077,hydrothermal_ceramic_synthesis,"Nanocone-assembled 3D SnO2 was synthesized by a fa ... quentially, and dried in air at 60 degC overnight."
2179,10.1016/j.matlet.2015.03.109,hydrothermal_ceramic_synthesis,ZnO NGls were synthesized as reported previously w ... e product was calcined at 500 degC for 2 h in air.
2180,10.1016/j.physe.2015.11.040,hydrothermal_ceramic_synthesis,Carbon coated MoO3 nanowires were synthesized in t ... clave and kept in the furnace at 180 degC for 4 h.
2181,10.1016/j.apsusc.2015.08.032,hydrothermal_ceramic_synthesis,All chemicals used in this experiment were of anal ... nd then dried in a vacuum oven at 60 degC for 6 h.
2182,10.1016/j.apsusc.2014.10.129,hydrothermal_ceramic_synthesis,TNTs were synthesized through an alkaline hydrothe ... grinded and sieved (200 mesh). TNTs were obtained.
2183,10.1016/j.cej.2015.03.125,hydrothermal_ceramic_synthesis,"X-shaped hollow α-FeOOH nanostructures were synthe ... nd ethanol, and finally dried at 60 degC for 12 h."
2184,10.1016/j.matlet.2013.01.080,hydrothermal_ceramic_synthesis,"MnCO3 was newly-prepared by Na2CO3 and MnCl2 solut ... , and then dried overnight in an oven at 110 degC."
2185,10.1016/j.cplett.2004.02.074,hydrothermal_ceramic_synthesis,"The start materials used in this research were che ... t 60 degC, black powders were ultimately obtained."
2186,10.1016/j.matchemphys.2010.07.027,hydrothermal_ceramic_synthesis,"All the chemicals were of analytical grade and use ... e ethanol, then finally dried at 100 degC for 8 h."
2187,10.1016/j.jallcom.2010.10.204,hydrothermal_ceramic_synthesis,"A 1.38 g of ammonium metatungstate hydrate ((NH4)6 ...  water and ethanol, and dried at 70 degC for 12 h."
2188,10.1016/j.cplett.2006.02.082,hydrothermal_ceramic_synthesis,"In a typical experimental procedure for preparing  ... ral times, and dried in vacuum at 50 degC for 6 h."
2189,10.1016/j.electacta.2008.09.071,hydrothermal_ceramic_synthesis,The α-Fe2O3 nanorods were synthesized via a hydrot ... ed by sintering the precursor at 500 degC for 2 h.
2190,10.1016/j.mseb.2008.09.023,hydrothermal_ceramic_synthesis,"First, Zn(NO3)2*6H2O (2 mmol), Al(NO3)3*9H2O (4 mm ... s, and then dried under vacuum at 80 degC for 6 h."
2191,10.1016/j.solmat.2015.10.022,hydrothermal_ceramic_synthesis,"20 mL of KI (0.5 M) ethylene glycol solution was a ... hree times, and finally dried at 80 degC for 12 h."
2192,10.1016/j.cej.2016.05.100,hydrothermal_ceramic_synthesis,All reagents used were of analytical grade and use ... n at 80 degC for 12 h to obtain the final product.
2193,10.1016/j.apsusc.2015.08.037,hydrothermal_ceramic_synthesis,"All the chemical reagents were of analytical purit ...  for several times, and dried at 60 degC for 12 h."
2194,10.1016/j.cej.2013.10.028,hydrothermal_ceramic_synthesis,"First, tetrabutyl titanate (TBT) was added dropwis ... degC before being calcined at 400 degC for 60 min."
2195,10.1016/j.jallcom.2013.11.075,hydrothermal_ceramic_synthesis,"In a typical synthesis, 2 mmol of Ba(Ac)2 (0.511 g ... ir to a constant weight for further investigation."
2196,10.1016/j.electacta.2016.01.161,hydrothermal_ceramic_synthesis,POMs@MOFs was synthesized according to a previous  ... POMs@MOFs was dried in vacuum at 80 degC for 72 h.
2197,10.1016/j.physe.2012.06.025,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.5 mL of butyl titanate a ... 60 degC. As a result, white powders were obtained."
2198,10.1016/j.jallcom.2009.08.127,hydrothermal_ceramic_synthesis,"FeCl3*6H2O (2 mmol) and thiourea (4 mmol) were dis ... s, and then dried under vacuum at 60 degC for 6 h."
2199,10.1002/smll.201303836,hydrothermal_ceramic_synthesis,"Preparation of α-MnO2 Nanowires: Ultralong α-MnO2  ...  for several times, followed by drying at 60 degC."
2200,10.1016/j.matlet.2009.01.057,hydrothermal_ceramic_synthesis,Na2Ti3O7 nanowires were synthesized through a simp ...  at 80 degC for 24 h to obtain Na2Ti3O7 nanowires.
2201,10.1002/asia.201301704,hydrothermal_ceramic_synthesis,The FeOx-propanediol lamellar precursor was synthe ... entrifugation and then dried at 60 degC overnight.
2202,10.1016/j.jallcom.2008.12.025,hydrothermal_ceramic_synthesis,"In a typical experiment, 2 mmol CoCl2 and 5 mmol N ...  calcined at 500 degC for 2 h in a muffle furnace."
2203,10.1016/j.matlet.2015.02.021,hydrothermal_ceramic_synthesis,"Preparation of the BiVO4sample: In a typical synth ... gC for 6 h, and then calcined at 400 degC for 5 h."
2204,10.1016/j.apcatb.2010.05.022,hydrothermal_ceramic_synthesis,All chemicals were analytically pure and used with ...  with deionized water and dried at 80 degC in air.
2205,10.1016/j.jcis.2016.03.046,hydrothermal_ceramic_synthesis,The Bi4O5Br2 nanosheets photocatalyst was synthesi ... ized by the same process without the pH adjusting.
2206,10.1016/j.snb.2013.10.127,hydrothermal_ceramic_synthesis,"ZnFe2O4 MNPs were synthesized by a hydrothermal me ... ree times, and then dried under ambient condition."
2207,10.1016/j.jallcom.2015.05.204,hydrothermal_ceramic_synthesis,"The α-Fe2O3 nanorings were synthesized by a hydrot ... everal times, and finally dried in air at 80 degC."
2208,10.1016/j.molcata.2014.10.002,hydrothermal_ceramic_synthesis,The TiO2 nanobelts were synthesized via a typical  ... re obtained by heat treatment for 2 h at 600 degC.
2209,10.1016/j.jallcom.2013.05.148,hydrothermal_ceramic_synthesis,"In a typical synthesis, 2.5 mmol of CoCl2[?]6H2O w ... lar procedures in the absence of GO [27] and [28]."
2210,10.1016/j.matlet.2007.03.036,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade and used as ... . The final product was dried at 70 degC for 24 h.
2211,10.1016/j.tsf.2014.12.037,hydrothermal_ceramic_synthesis,All chemical reagents were of analytic purity and  ...  and dried in vacuum at 60 degC for more than 4 h.
2212,10.1016/j.jpcs.2009.07.014,hydrothermal_ceramic_synthesis,"To obtain CdS nanoparticles, 0.1464 g Cd(OH)2 and  ... red sample was dried in vacuum at 60 degC for 6 h."
2213,10.1016/j.apcatb.2015.05.044,hydrothermal_ceramic_synthesis,"TiO2 support [23] ; [24] was prepared by a hydroth ... eral times, and finally dried at 70 degC for 12 h."
2214,10.1016/j.electacta.2015.01.018,hydrothermal_ceramic_synthesis,The Ni-Co precursors were first prepared by a simp ... l for several times to remove the ethylene glycol.
2215,10.1007/s10854-009-9950-z,hydrothermal_ceramic_synthesis,"Hollow BNdT microspheres were synthesized by hydro ... ethanol, and then dried at 80 degC in air for 6 h."
2216,10.1016/j.jallcom.2014.11.137,hydrothermal_ceramic_synthesis,"The synthesis of CuS without surfactant was as fol ... thanol, and dried in a vacuum at 60 degC for 12 h."
2217,10.1016/j.jssc.2009.07.038,hydrothermal_ceramic_synthesis,"ZnO nanorods (0.081 g) and thioacetamide (TAA, 0.0 ... duct was dried in a vacuum box at 50 degC for 4 h."
2218,10.1002/cplu.201500534,hydrothermal_ceramic_synthesis,"In a typical process, stoichiometric amounts of Fe ... eral times before being dried at 60 degC for 12 h."
2219,10.1016/j.tsf.2012.01.002,hydrothermal_ceramic_synthesis,Alkali hydrothermal method was used for the prepar ... e was finally calcined at 500 degC for 2 h in air.
2220,10.1016/j.jssc.2010.12.013,hydrothermal_ceramic_synthesis,Monoclinic CdWO4 Appropriate amounts of Na2WO4*2H2 ... so prepared according to this hydrothermal method.
2221,10.1016/j.jallcom.2013.07.026,hydrothermal_ceramic_synthesis,"The magnetite nanoparticles were prepared accordin ... d by a magnet for several times, and dried in air."
2222,10.1002/aoc.3432,hydrothermal_ceramic_synthesis,"Bi(NO3)3[?]5H2O (0.645 g, 1.33 mmol) was dissolved ... egC in air overnight for further characterization."
2223,10.1016/j.jssc.2010.04.001,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.3 mmol CdCl2, 0.12 g PVP ... ducts but the other conditions were kept the same."
2224,10.1016/j.matlet.2015.12.159,hydrothermal_ceramic_synthesis,"Nanorod-assembled porous α-MoO3 sponges were synth ... , to the formation of monodispersed MoO3 nanorods."
2225,10.1016/j.jpowsour.2014.07.093,hydrothermal_ceramic_synthesis,"For comparison, β-MnO2 hollow nanorods were synthe ... 1D hollow β-MnO2 nanorods were got, named as Srod."
2226,10.1016/j.apsusc.2011.04.081,hydrothermal_ceramic_synthesis,"In a typical synthesis [21], 12 mL Te NWs aqueous  ... d water and absolute ethanol and dried at 60 degC."
2227,10.1016/j.electacta.2017.02.020,hydrothermal_ceramic_synthesis,"To prepare nano-spinel NiFe2O4, powders of Fe(NO3) ... water), and dried under vacuum at 80 degC for 5 h."
2228,10.1016/j.matchemphys.2007.05.016,hydrothermal_ceramic_synthesis,All chemicals (analytical grade reagents) were pur ... then finally dried in a vacuum at 60 degC for 4 h.
2229,10.1016/j.matlet.2016.05.113,hydrothermal_ceramic_synthesis,All the chemical reagents used in the experiment w ... same procedure while without the addition of EDTA.
2230,10.1016/j.jcat.2015.02.016,hydrothermal_ceramic_synthesis,CeO2 support was prepared by a hydrothermal method ...  degC/min and calcined in air at 450 degC for 4 h.
2231,10.1016/j.matlet.2012.08.074,hydrothermal_ceramic_synthesis,All the chemicals were of analytical grade and use ...  in sequence and dried in air at 80 degC for 12 h.
2232,10.1016/j.solidstatesciences.2014.03.001,hydrothermal_ceramic_synthesis,SnS2-graphene nanocomposites were prepared by a hy ...  several times and dried in air at 333 K for 12 h.
2233,10.1016/j.ssc.2004.03.021,hydrothermal_ceramic_synthesis,Cd0.9Mn0.1S nanorods were hydrothermally prepared  ... r 4 h and were collected for the characterization.
2234,10.1007/s10008-013-2372-0,hydrothermal_ceramic_synthesis,"First, 15 mL of KMnO4 (4 mmol) aqueous solution wa ... nthesised product was referred to as undoped MnO2."
2235,10.1016/j.matlet.2015.09.123,hydrothermal_ceramic_synthesis,The mesoporous NiO nanourchins powder was synthesi ... or 12 h and then was annealed at 400 degC for 3 h.
2236,10.1016/j.jphotochem.2016.03.036,hydrothermal_ceramic_synthesis,All reagents were of analytical grade and used wit ... hese products in a vacuum oven at 60 degC for 6 h.
2237,10.1016/j.electacta.2016.05.006,hydrothermal_ceramic_synthesis,All chemicals were obtained from commercial source ...  sample has been proved by XRD analysis (Fig. S1).
2238,10.1016/j.jlumin.2006.09.006,hydrothermal_ceramic_synthesis,"The starting materials were Gd2O3 (99.9%), La2O3 ( ... cipitation method and treated at 900 degC for 2 h."
2239,10.1016/j.poly.2004.03.004,hydrothermal_ceramic_synthesis,JGP-5 was hydrothermally prepared from a reaction  ... d overnight at 50 degC to give colorless crystals.
2240,10.1016/j.electacta.2012.10.109,hydrothermal_ceramic_synthesis,Nanorods of α-MnO2 were synthesized based on our p ... ods was then obtained after vacuum-dry at 40 degC.
2241,10.1016/j.apsusc.2012.09.039,hydrothermal_ceramic_synthesis,"In first step, the lanthanum doped TiO2 samples we ... mic ratios of La to TiO2 were 0.2%, 0.9% and 1.8%."
2242,10.1002/asia.201403198,hydrothermal_ceramic_synthesis,"Synthesis of α-NiS hollow spheres: 0.16 g of nicke ... several times, and then dried at 50 degC for 12 h."
2243,10.1007/s10854-012-0623-y,hydrothermal_ceramic_synthesis,"In a typical synthesis, 1 g FeCl2*4H2O was dissolv ... ts were dried in a vacuum oven at 50 degC for 8 h."
2244,10.1016/j.electacta.2013.11.077,hydrothermal_ceramic_synthesis,"The Na0.35MnO2 nanowire was prepared by a hydrothe ... with water three times, and then dried at 60 degC."
2245,10.1016/j.apsusc.2014.07.092,hydrothermal_ceramic_synthesis,"The BiErWO6 photocatalyst was synthesized through  ... several times, and then dried at 60 degC for 12 h."
2246,10.1016/j.jssc.2011.11.045,hydrothermal_ceramic_synthesis,"Cu-embedded carbon spheres (C-CS) were prepared by ... ely, corresponding to the concentration of copper."
2247,10.1016/j.solidstatesciences.2012.08.029,hydrothermal_ceramic_synthesis,"All the chemical reagents were purchased from Shan ... s, and then dried in a vacuum at 50 degC for 12 h."
2248,10.1016/j.materresbull.2011.05.019,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade purity, and ... roducts were further calcined at 550 degC for 4 h."
2249,10.1016/j.matlet.2014.12.128,hydrothermal_ceramic_synthesis,Synthesis of ZnS nanoparticles: Solvothermal treat ...  the white material was dried at 120 degC for 2 h.
2250,10.1016/j.materresbull.2014.11.022,hydrothermal_ceramic_synthesis,"In a typical synthesis, FeCl2*4H2O (0.15 mmol) and ... 0 degC for 5 h. Finally black powder was obtained."
2251,10.1016/j.materresbull.2009.05.024,hydrothermal_ceramic_synthesis,"0.1497 g of CuSO4*5H2O (0.6 mmol) was dissolved in ... ethanol, and then vacuum dried at 60 degC for 4 h."
2252,10.1016/j.materresbull.2014.07.008,hydrothermal_ceramic_synthesis,"In our experiment, α-Fe2O3 nanoellipses were synth ... ethanol several times and dried at 60 degC in air."
2253,10.1016/j.jpowsour.2014.07.114,hydrothermal_ceramic_synthesis,"In a typically synthesis, 25 mg H2Ti3O7 (or TiO2)  ... on and dried at 60 degC for 12 h in a vacuum oven."
2254,10.1016/j.powtec.2012.10.060,hydrothermal_ceramic_synthesis,"All reagents used in the experiment were of analyt ... ly, the product was dried under vacuum at 60 degC."
2255,10.1016/j.electacta.2014.05.068,hydrothermal_ceramic_synthesis,Synthesis of amorphous FeOOH and α-FeOOH. All chem ... the same as those for amorphous FeOOH preparation.
2256,10.1016/j.matchemphys.2004.04.001,hydrothermal_ceramic_synthesis,All chemicals (analytical grade reagents) were pur ... then finally dried in a vacuum at 60 degC for 4 h.
2257,10.1016/j.matlet.2006.03.073,hydrothermal_ceramic_synthesis,"All the analytical chemicals were purchased from S ... al times, and dried in vacuum at 50 degC for 12 h."
2258,10.1016/j.solidstatesciences.2015.12.013,hydrothermal_ceramic_synthesis,All reagents were used as received without further ...  with distilled water and dried in air at 60 degC.
2259,10.1016/j.matlet.2014.10.026,hydrothermal_ceramic_synthesis,"The hydrothermal method was employed to synthesize ... stilled water, and then dried at 80 degC for 12 h."
2260,10.1016/j.matlet.2009.11.008,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.2 g of ZnO powder was pu ... with distilled water, and dried in air at 80 degC."
2261,10.1016/j.matlet.2015.10.155,hydrothermal_ceramic_synthesis,All the chemicals were of analytic grade and used  ... out the addition of SDS under the same conditions.
2262,10.1016/j.matlet.2014.07.005,hydrothermal_ceramic_synthesis,Preparation of carbon spheres: Glucose (4 g) was d ... ethanol several times and dried at 60 degC in air.
2263,10.1016/j.jallcom.2013.04.146,hydrothermal_ceramic_synthesis,All of the reagents used were of analytical purity ... cined at 600 degC for 3 h to obtain Mn2O3 product.
2264,10.1016/j.jpcs.2016.06.002,hydrothermal_ceramic_synthesis,NBT:Er nanocrystals were synthesized via a hydroth ... powders were annealed at 600 degC for 12 h in air.
2265,10.1016/j.jpowsour.2016.06.065,hydrothermal_ceramic_synthesis,Mesoporous CuCo2O4 were synthesized through a urea ... 300 degC for 3 h to obtain the mesoporous CuCo2O4.
2266,10.1016/j.matlet.2016.05.166,hydrothermal_ceramic_synthesis,"All the chemicals were of analytical grade and use ... ol and distilled water, and then dried at 80 degC."
2267,10.1016/j.matchemphys.2012.07.040,hydrothermal_ceramic_synthesis,"A Co(NO3)2*6H2O aqueous solution (200 mg of Co(NO3 ... ter and ethanol three times, and dried at 60 degC."
2268,10.1016/j.cej.2013.02.009,hydrothermal_ceramic_synthesis,CuFe2O4 MNPs were prepared using a hydrothermal me ... l times with ethanol and dried at 60 degC for 6 h.
2269,10.1016/j.mseb.2010.07.023,hydrothermal_ceramic_synthesis,All reagents used in the experiments were of analy ...  in vacuum at 75 degC for future characterization.
2270,10.1007/s10853-014-8445-3,hydrothermal_ceramic_synthesis,"Bi2WO6 photocatalyst was prepared by a hydrotherma ... several times, and then dried at 60 degC for 12 h."
2271,10.1016/j.apcatb.2015.12.027,hydrothermal_ceramic_synthesis,BiVO4 with {1 1 0} and {0 1 0} facets exposed was  ... ts were dried at 60 degC overnight in vacuum oven.
2272,10.1016/j.matlet.2008.03.031,hydrothermal_ceramic_synthesis,"In our experiments, all of the chemical reagents u ... degC for 6 h. The black-red powders were obtained."
2273,10.1016/j.jallcom.2010.10.154,hydrothermal_ceramic_synthesis,The synthesis of V3O7*H2O nanobelts was based on o ...  were represented in Fig. S1 (Supplementary data).
2274,10.1016/j.energy.2016.01.061,hydrothermal_ceramic_synthesis,"KMnO4, polyethylene glycol 400 (PEG-400) and DI wa ... as washed with DI water and ethanol several times."
2275,10.1016/j.matlet.2009.01.040,hydrothermal_ceramic_synthesis,"In a typical process, 0.042 g AgNO3 was dissolved  ... h different molar ratios of dodecylamine to AgNO3."
2276,10.1016/j.electacta.2014.04.013,hydrothermal_ceramic_synthesis,"SnO2 echinus-like nanospheres were fabricated by a ... nol and water, and then dried at 60 degC for 12 h."
2277,10.1007/s10854-016-6004-1,hydrothermal_ceramic_synthesis,"In a typical synthesis of PbWO4: Sm3+, stoichiomet ... concentration for the samples was taken as 5 at.%."
2278,10.1016/j.carbon.2004.04.024,hydrothermal_ceramic_synthesis,"In a typical experiment, nickel oxide (NiO) powder ... d sample was dried in a vacuum at 65 degC for 6 h."
2279,10.1016/j.matlet.2015.12.015,hydrothermal_ceramic_synthesis,"In a typical synthesis, 2 mmol of Sr(Ac)2*0.5H2O ( ... ol in sequence, and then dried at 100 degC in air."
2280,10.1007/s10854-016-5627-6,hydrothermal_ceramic_synthesis,"The GNS was prepared by a modified Hummers method  ... times, and finally dried at 60 degC for 24 h [34]."
2281,10.1016/j.matlet.2005.07.015,hydrothermal_ceramic_synthesis,The reaction was carried out in a 50 ml capacity T ... annel like tellurium product was finally produced.
2282,10.1016/j.matlet.2012.01.013,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.0075 mol of glycol was a ... e (ED) were also used in the parallel experiments."
2283,10.1016/j.ssc.2005.03.004,hydrothermal_ceramic_synthesis,"All the analytical chemicals were purchased from S ... imes, and then dried in vacuum at 60 degC for 4 h."
2284,10.1016/j.colsurfa.2011.12.058,hydrothermal_ceramic_synthesis,All of the reagents were of analytical grade and w ... dried in vacuum at 75 degC for future application.
2285,10.1007/s10854-016-5110-4,hydrothermal_ceramic_synthesis,"All the reagents in the present investigation were ... g ratio of Zn:S to 1:2, 1:4 and 1:6, respectively."
2286,10.1016/j.ijhydene.2014.11.058,hydrothermal_ceramic_synthesis,"All of the reagents were of analytical grade and u ... veral times, and dried in air at 80 degC for 12 h."
2287,10.1016/j.cplett.2005.01.050,hydrothermal_ceramic_synthesis,"In a typical procedure, FeCl3 * 6H2O or FeSO4 * 7H ... imes, and then dried in vacuum at 60 degC for 4 h."
2288,10.1016/j.matlet.2007.06.057,hydrothermal_ceramic_synthesis,"Glucose was dissolved in distilled water (80 mL, 0 ... 1 degC min- 1 for 3 h using a tube furnace in air."
2289,10.1016/j.matlet.2015.12.131,hydrothermal_ceramic_synthesis,A typical synthesis procedure of the porous SrCO3  ... hanol and then dried at 80 degC in vacuum for 6 h.
2290,10.1016/j.matlet.2013.06.065,hydrothermal_ceramic_synthesis,All reagents used were of analytical purity and we ... products were put in the oven at 380 degC for 2 h.
2291,10.1016/j.matlet.2009.07.020,hydrothermal_ceramic_synthesis,"In a typical synthesis, 1, 5, 10, and 30 mL of 10  ... while the samples were cooled to room temperature."
2292,10.1016/j.matlet.2010.10.083,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade and used as ... n of the tellurium/calcium silicate nanocomposite.
2293,10.1016/j.matlet.2010.05.007,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.56 g TiO2 nanowires are  ... ed water, and dried in air at ambient temperature."
2294,10.1016/j.cplett.2005.03.141,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.4 g In(S2CNEt2)3 complex ... eral times and dried in vacuum at 50 degC for 6 h."
2295,10.1016/j.mseb.2008.09.017,hydrothermal_ceramic_synthesis,"In a typical procedure, 20 ml 0.5 M NaOH solution  ... duct was dried in a vacuum box at 50 degC for 4 h."
2296,10.1016/j.elecom.2006.10.008,hydrothermal_ceramic_synthesis,"Rutile TiO2 powders were prepared using a sol-gel  ... 0 degC for 24 h, the TiO2 nanotubes were obtained."
2297,10.1016/j.matlet.2014.05.034,hydrothermal_ceramic_synthesis,CuO microstructures were synthesized via a hydroth ... the products were dried in air at 80 degC for 3 h.
2298,10.1016/j.jpowsour.2015.07.074,hydrothermal_ceramic_synthesis,"Typically, 0.164 g PEG-20000 was dissolved and sti ... ized water for three times, and then freeze-dried."
2299,10.1016/j.jpowsour.2014.03.011,hydrothermal_ceramic_synthesis,FeS2 particle was synthesized by a simply hydrothe ... times and dried at 70 degC under vacuum overnight.
2300,10.1016/j.jallcom.2016.08.321,hydrothermal_ceramic_synthesis,"MnO2 nanorods were synthesized here by using MnSO4 ... tion. Finally, the products were dried at 50 degC."
2301,10.1016/j.jelechem.2013.12.030,hydrothermal_ceramic_synthesis,Graphene oxide (GO) was prepared from natural grap ... tained by drying at 60 degC under vacuum for 12 h.
2302,10.1016/j.apsusc.2017.02.198,hydrothermal_ceramic_synthesis,Preparation of ZnFe2O4 samples by hydrothermal met ... at 60 degC for 6 h to obtain the ZnFe2O4 products.
2303,10.1016/j.solidstatesciences.2014.03.018,hydrothermal_ceramic_synthesis,In a typical synthesis of spindle like BiVO4 sampl ... up of the products was described in Section 2.1.1.
2304,10.1016/j.matlet.2016.01.031,hydrothermal_ceramic_synthesis,"All the chemical reagents were of analytical purit ... for several times, and dried at 60 degC overnight."
2305,10.1016/j.jallcom.2014.11.087,hydrothermal_ceramic_synthesis,"The THSs were synthesized by a one-pot hydrotherma ... d deionized water, then dried at 60 degC for 24 h."
2306,10.1007/s10854-016-5156-3,hydrothermal_ceramic_synthesis,"In brief, 1.5 g of FeCl3*6H2O was dissolved in 60  ... , and then dried under vacuum at 60 degC for 12 h."
2307,10.1002/ejic.200601131,hydrothermal_ceramic_synthesis,"Synthetic Procedures: KOH, NaOH, and Nb2O5 (all ar ... istilled water and ethanol, then dried at 80 degC."
2308,10.1007/s10853-011-5779-y,hydrothermal_ceramic_synthesis,"FeCl3*6H2O (1.35 g, 5 mmol) was dissolved in ethyl ...  times with ethanol and dried at 80 degC for 12 h."
2309,10.1016/j.solidstatesciences.2014.03.009,hydrothermal_ceramic_synthesis,All of the chemicals were analytical grade and use ... taining InVO4 porous microspheres for further use.
2310,10.1016/j.jpowsour.2013.06.027,hydrothermal_ceramic_synthesis,"In a typical procedure, 200 mg of precursors and 6 ... or 12 h. These samples were denominated as Co-S-T."
2311,10.1016/j.matlet.2013.02.009,hydrothermal_ceramic_synthesis,"SnS2 powder (120 mg) was dispersed in distilled wa ...  as SnS2/TiO2-17, 23, 26, 29 and 33, respectively."
2312,10.1016/j.electacta.2014.11.042,hydrothermal_ceramic_synthesis,CoFe2O4 solid nanospheres were also synthesized th ... ith deionized water and ethanol for several times.
2313,10.1016/j.materresbull.2014.05.032,hydrothermal_ceramic_synthesis,Ag2WO4 microrods were prepared by using silver-amm ...  and ethanol and finally dried at 60 degC for 6 h.
2314,10.1016/j.mssp.2011.02.019,hydrothermal_ceramic_synthesis,Bi2Te3 was prepared by a hydrothermal route. In a  ... e ethyl alcohol and then dried in vacuum at 333 K.
2315,10.1007/s10854-016-4606-2,hydrothermal_ceramic_synthesis,All chemicals were obtained commercially and used  ... tation dried in a vacuum oven at 60 degC for 12 h.
2316,10.1016/j.ssc.2011.11.036,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.50 g of V O2(B) powder w ...  in vacuum at 75 degC for future characterization."
2317,10.1016/j.apcatb.2016.05.042,hydrothermal_ceramic_synthesis,"The Bi4O5I2 nanoflakes were synthesized using a so ... me procedure, but KI was replaced by 1.5 mmol KBr."
2318,10.1007/s10876-012-0478-7,hydrothermal_ceramic_synthesis,"To synthesize OMS-2 nanotubes, a hydrothermal meth ... tilled water and ethanol, vacuum dried at 80 degC."
2319,10.1016/j.jpowsour.2014.05.037,hydrothermal_ceramic_synthesis,"Firstly, MWCNT@CoS1.097 nanocomposites were prepar ... rmogravimetric analysis in our previous work [30]."
2320,10.1016/j.apsusc.2017.03.256,hydrothermal_ceramic_synthesis,All reagents used in the experiment were of analyt ... roduct was dried under vacuum at 60 degC for 12 h.
2321,10.1016/j.ssc.2004.02.008,hydrothermal_ceramic_synthesis,"The reagent Mg2Si was of 99.5% purity from Alfa Ae ...  degC for 4 h, a gray powder product was obtained."
2322,10.1016/j.solidstatesciences.2013.11.001,hydrothermal_ceramic_synthesis,"Chemical reagents of (NH4)2S2O8, MnSO4*H2O, and (N ... sulting samples were air-dried at 80 degC for 8 h."
2323,10.1016/j.apsusc.2017.01.294,hydrothermal_ceramic_synthesis,All the reagents were analytical grades and were u ... e hierarchical Bi2WO6 architectures were obtained.
2324,10.1016/j.jssc.2008.05.006,hydrothermal_ceramic_synthesis,Here we adopted the hydrothermal carbonization co- ... ispersed in absolute ethanol for characterization.
2325,10.1002/asia.201300771,hydrothermal_ceramic_synthesis,All reagents were of analytical grade and used wit ... d by the hydrothermal route in the absence of PVP.
2326,10.1007/s10854-017-6548-8,hydrothermal_ceramic_synthesis,"The α-Fe2O3/SnO2 hybrids were synthesized via a fa ... . The products were assigned as C-1, C-2, and C-3."
2327,10.1016/j.msec.2013.05.037,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.485 g of Bi(NO3)3 * 5H2O ... nol, respectively, and dried in vacuum at 60 degC."
2328,10.1016/j.matlet.2005.12.027,hydrothermal_ceramic_synthesis,Solvothermal method was employed to synthesize Co1 ... ained powders were collected for characterization.
2329,10.1016/j.matchemphys.2014.04.025,hydrothermal_ceramic_synthesis,The colloidal carbon spheres were synthesized from ... es and dried at room temperature in a vacuum oven.
2330,10.1016/j.apcatb.2012.02.033,hydrothermal_ceramic_synthesis,The tremelliform Co0.85Se nanosheets were synthesi ... m at 60 degC for 4 h for further characterization.
2331,10.1016/j.jpowsour.2013.06.027,hydrothermal_ceramic_synthesis,"In a typical synthesis, the nanorods of precursors ... here T refers to the temperature of precipitation."
2332,10.1016/j.electacta.2011.09.004,hydrothermal_ceramic_synthesis,"Synthesis route A: LiOH*H2O (95.0%, Aladdin) and i ...  yield LiFePO4/C, which was designated as LFP/C-A."
2333,10.1016/j.jallcom.2015.03.100,hydrothermal_ceramic_synthesis,"The precursors were synthesized by a modified hydr ... were labeled Q150, Q170, Q190, Q210, respectively."
2334,10.1016/j.jpcs.2010.10.087,hydrothermal_ceramic_synthesis,TiO2 powder was synthesized by the hydrothermal me ... everal times and finally dried at 80 degC for 6 h.
2335,10.1016/j.matlet.2007.01.091,hydrothermal_ceramic_synthesis,"Sodium selenite (Na2SeO3) was purchased from Sigma ... hed with distilled water, and air-dried overnight."
2336,10.1016/j.electacta.2015.05.086,hydrothermal_ceramic_synthesis,"Secondly, MoS2 nanosheets were uniformly coated wi ... for several times, and dried in vacuum at 60 degC."
2337,10.1016/j.mseb.2011.07.004,hydrothermal_ceramic_synthesis,"Typically, a total 40 mL of glucose aqueous soluti ... l five times and dried at 60 degC for 12 h in air."
2338,10.1016/j.matlet.2015.06.033,hydrothermal_ceramic_synthesis,"The RS-AgCl@Ag was prepared by a one-pot hydrother ... thanol several times, dried in an oven at 60 degC."
2339,10.1016/j.jhazmat.2013.11.032,hydrothermal_ceramic_synthesis,All chemicals used were purchased and used without ... owder was then freeze-dried under vacuum for 12 h.
2340,10.1016/j.orgel.2014.08.020,hydrothermal_ceramic_synthesis,The anatase titanium dioxide nanotubes were prepar ... egC for 2 h to crystallize into the anatase phase.
2341,10.1002/asia.201500319,hydrothermal_ceramic_synthesis,Synthesis of WO3-x nanowires: In a typical procedu ... fferent temperatures followed the same procedures.
2342,10.1016/j.matlet.2013.02.031,hydrothermal_ceramic_synthesis,All the chemicals were purchased from WAKO chemica ... s were collected and annealed at 200 degC for 3 h.
2343,10.1016/j.jpowsour.2013.09.047,hydrothermal_ceramic_synthesis,MnO2 nanorods were synthesized by a hydrothermal m ... ashing with distilled water and drying at 60 degC.
2344,10.1002/celc.201600051,hydrothermal_ceramic_synthesis,MIL-88 (Fe) was obtained through a hydrothermal me ... led water via centrifugation/re-dispersion cycles.
2345,10.1016/j.apcatb.2011.08.042,hydrothermal_ceramic_synthesis,"Typically, 1 mmol of Bi(NO3)3*5H2O and 2 mmol of F ... several times, and then dried at 60 degC for 12 h."
2346,10.1016/j.optmat.2012.08.021,hydrothermal_ceramic_synthesis,"In a typical synthesis, 2 mmol of Ba(Ac)2 (0.511 g ... ried in air at 50 degC to obtain the final sample."
2347,10.1007/s10854-016-4364-1,hydrothermal_ceramic_synthesis,"In a typical hydrothermal process, 0.45 g Na2SnO3* ... nally dried at 60 degC for 24 h to get the powder."
2348,10.1002/smll.201401521,hydrothermal_ceramic_synthesis,"Synthesis of Nanostructured MoS2: All chemicals we ... e, and dried in a vacuum oven at 80 degC for 12 h."
2349,10.1007/s10854-013-1375-z,hydrothermal_ceramic_synthesis,All of the reagents and solvents were analytical g ...  product was dried in a vacuum at 60 degC for 4 h.
2350,10.1016/j.matlet.2012.04.096,hydrothermal_ceramic_synthesis,"Titanate Ho3 +-Yb3 + codoped nanotubes were synthe ... es of nanotubes are labeled TiRT, Ti100 and Ti280."
2351,10.1016/j.electacta.2016.05.214,hydrothermal_ceramic_synthesis,MnO2 was grown on the surface of the CNFs/MnOx com ...  several times and then dried at 60 degC for 12 h.
2352,10.1016/j.ssc.2005.06.033,hydrothermal_ceramic_synthesis,"In a typical procedure, the as-prepared brown prod ... ral times, and dried at 60 degC for 4 h in vacuum."
2353,10.1016/j.solidstatesciences.2016.04.005,hydrothermal_ceramic_synthesis,"In a typical synthesis, carbonaceous spheres are f ... before vacuum-drying at room temperature for 24 h."
2354,10.1016/j.matchemphys.2016.06.074,hydrothermal_ceramic_synthesis,All chemicals used here were analytical-grade and  ... solute ethanol and being dried at 333 K overnight.
2355,10.1016/j.cplett.2014.08.011,hydrothermal_ceramic_synthesis,GdOOH:Eu3+ (4 mol% Eu) nanorods were prepared by t ... 0 degC for 4 h to prepare the GdOOH:Eu3+ nanorods.
2356,10.1016/j.matlet.2013.06.020,hydrothermal_ceramic_synthesis,"Firstly, 4 mmol of Bi(NO3)2*5H2O and 6 mmol of l-c ... respectively, and then dried at 80 degC overnight."
2357,10.1016/j.electacta.2013.10.116,hydrothermal_ceramic_synthesis,"All the reagents were of analytical grade and used ... powder gave a yield of 89 at%, as calculated from:"
2358,10.1016/j.matchemphys.2011.08.056,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade and were us ... ater and ethanol, vacuum dried at 60 degC for 6 h."
2359,10.1016/j.jssc.2016.05.018,hydrothermal_ceramic_synthesis,All chemicals were used from commercial sources wi ... ed with deionized water. Yield: 40% based on lead.
2360,10.1007/s00339-014-8667-x,hydrothermal_ceramic_synthesis,The carbon-coated AgNWs were prepared via hydrothe ... d and washed with deionized water for three times.
2361,10.1016/j.jallcom.2015.10.006,hydrothermal_ceramic_synthesis,MnO2 was synthesized by a hydrothermal method acco ... ashing with distilled water and drying at 60 degC.
2362,10.1016/j.scriptamat.2014.06.030,hydrothermal_ceramic_synthesis,"In our experiment, FeWO4 nanowires were prepared b ... d water and ethanol and dried at 60 degC for 12 h."
2363,10.1016/j.chroma.2015.04.057,hydrothermal_ceramic_synthesis,"The magnetic Fe3O4 particles were prepared accordi ...  overnight at 60 C, and calcined at 400 C for 2 h."
2364,10.1016/j.jelechem.2015.09.043,hydrothermal_ceramic_synthesis,Graphene oxide (GO) was synthesized by the modifie ... e dried in vacuum desiccators at room temperature.
2365,10.1016/j.jcis.2011.08.073,hydrothermal_ceramic_synthesis,TiO2 HSs were synthesized by the chemically induce ... ct was dried in a vacuum oven at 80 degC for 12 h.
2366,10.1016/j.matlet.2007.05.046,hydrothermal_ceramic_synthesis,"Cupric nitrate (Cu(NO3)2*3H2O), sodium hydroxide(N ... anol, and dried under vacuum overnight at 40 degC."
2367,10.1016/j.ica.2008.07.011,hydrothermal_ceramic_synthesis,Sodium metasilicate (18.94 g) was dissolved in de- ... i-MCM-41 and 0.007-0.02 for Al-MCM-41 or V-MCM-41.
2368,10.1016/j.electacta.2014.09.060,hydrothermal_ceramic_synthesis,"Typically, 10 mmol tetrabutyl titanate (TBT) and 2 ... rsor was calcined in a muffle oven in air for 5 h."
2369,10.1016/j.jpowsour.2015.01.156,hydrothermal_ceramic_synthesis,0.5 g of Mn(CH3COO)2*4H2O was added to 5 ml of dis ...  by centrifugation and dried at 90 degC overnight.
2370,10.1016/j.electacta.2016.02.190,hydrothermal_ceramic_synthesis,"All chemicals were used directly without further p ... ter, and then dried in vacuum at 80 degC for 12 h."
2371,10.1016/j.cej.2016.01.003,hydrothermal_ceramic_synthesis,"The typical synthesis of the 3D CCMs was carried o ... fter then, the 3D CCMs were successfully prepared."
2372,10.1016/j.materresbull.2007.01.017,hydrothermal_ceramic_synthesis,ZnO nanorods were prepared by using the following  ... ng (1 and 20 degC/min) were employed in the study.
2373,10.1016/j.matlet.2014.08.038,hydrothermal_ceramic_synthesis,Materials and method: All reagents were of analyti ... product was washed and dried for characterization.
2374,10.1016/j.jpowsour.2011.01.030,hydrothermal_ceramic_synthesis,Flower-like SnO2 nanostructures were synthesized b ... ing 0.03 g NaF instead of Na2SO4*5H2O in step (1).
2375,10.1016/j.elecom.2006.06.025,hydrothermal_ceramic_synthesis,CdS nanocrystalline powder was synthesized by a hy ... l and deionized water and dried at 50 degC in air.
2376,10.1016/j.jssc.2012.07.023,hydrothermal_ceramic_synthesis,"In a typical procedure, 35 mg of Cu(cup)2 was diss ...  were redispersed in ethanol for characterization."
2377,10.1007/s10853-007-2039-2,hydrothermal_ceramic_synthesis,"For Bi2S3 nanowires, 0.15 g Bi(NO3)3*5H2O, 0.04 g  ... muth sulfide but without the addition of thiourea."
2378,10.1016/j.jpcs.2011.08.031,hydrothermal_ceramic_synthesis,Cerium oxide nanostructures were synthesized under ...  the comparative experiments are shown in Table 1.
2379,10.1016/j.matchemphys.2007.10.002,hydrothermal_ceramic_synthesis,"In a typical synthesis procedure, 0.01 mol of anal ... , and kept in a sealed plastic bottle in the dark."
2380,10.1016/j.jelechem.2015.04.038,hydrothermal_ceramic_synthesis,The nanoplate-stacked Fe3O4 was synthesized throug ... nd finally dried at 50 degC under vacuum for 12 h.
2381,10.1016/j.jpowsour.2016.07.017,hydrothermal_ceramic_synthesis,"Similarly, the brookite TiO2 rice-like particles a ...  degC for 3 h with a heating rate of 2 degC min-1."
2382,10.1016/j.matlet.2015.08.118,hydrothermal_ceramic_synthesis,"A hydrothermal method was used to synthesize the C ... stilled water, finally dried at 60 degC overnight."
2383,10.1016/j.electacta.2009.09.021,hydrothermal_ceramic_synthesis,TiO2 hollow spheres were prepared by the CIST meth ... ct was dried in a vacuum oven at 80 degC for 12 h.
2384,10.1016/j.molcata.2007.03.027,hydrothermal_ceramic_synthesis,The support Ce0.8Zr0.2O2 was prepared via a hydrot ... uffle furnace for 4 h; yellow powder was obtained.
2385,10.1016/j.jpcs.2014.08.001,hydrothermal_ceramic_synthesis,"All chemicals were analytical-grade reagents and w ...  4, and 5 mol% Fe-doped ZnO powders were obtained."
2386,10.1016/j.matlet.2014.06.010,hydrothermal_ceramic_synthesis,"All reagents were of analytical-grade therefore us ... 5 g of KOH, keeping all other parameters constant."
2387,10.1016/j.matlet.2006.04.087,hydrothermal_ceramic_synthesis,"The purity of starting materials LiOH*H2O, LiNO3 a ... ynthesis used in this work were listed in Table 1."
2388,10.1016/j.jpcs.2009.12.023,hydrothermal_ceramic_synthesis,The mesoporous TiO2 microspheres were synthesized  ... s were dried in a vacuum oven at 80 degC for 12 h.
2389,10.1016/j.jallcom.2009.08.043,hydrothermal_ceramic_synthesis,The α-Fe2O3 nanowires were synthesized via a hydro ... d at 500 degC for 2 h to obtain α-Fe2O3 nanowires.
2390,10.1016/j.jallcom.2014.11.156,hydrothermal_ceramic_synthesis,"In brief, 0.01 mol KMnO4 and 1.5 g PVP (Mw = 40,00 ... deionized water and dried under vacuum at 80 degC."
2391,10.1016/j.apcatb.2015.04.017,hydrothermal_ceramic_synthesis,Na2WO4*2H2O (0.003 mol) and NH4Cl (0.01 mol) were  ... e of 1 degC/min and then rodlike WO3 was obtained.
2392,10.1002/cphc.201402010,hydrothermal_ceramic_synthesis,A 10 mL aqueous mixture of KMnO4 (0.2 mmol) and NH ... 30 minutes) and dried at 50 degC in a vacuum oven.
2393,10.1016/j.jallcom.2013.07.116,hydrothermal_ceramic_synthesis,"Analytical grade MnSO4*H2O (99.0%), NaClO3 (99.0%) ... water, and subsequently dried at room temperature."
2394,10.1016/j.electacta.2015.07.143,hydrothermal_ceramic_synthesis,The preparation of CuO/PrGO is presented in Scheme ...  the same procedures but using GR instead of PrGO.
2395,10.1016/j.matlet.2014.01.158,hydrothermal_ceramic_synthesis,"Synthesis of SnS2/WO3nanocomposite: 5.0 mmol SnCl4 ... ed water, and dried in vacuum at 100 degC for 4 h."
2396,10.1016/j.solidstatesciences.2012.02.003,hydrothermal_ceramic_synthesis,"The SnO2 nanospheres were prepared through a simpl ... terward, were dried in vacuum at 70 degC for 12 h."
2397,10.1016/j.electacta.2016.06.057,hydrothermal_ceramic_synthesis,"Initially, W3O8 nanorods were synthesized by hydro ... nt W3O8 nanorods precipitate was dried at 60 degC."
2398,10.1016/j.jpowsour.2016.04.139,hydrothermal_ceramic_synthesis,"Bulk CoS2 was synthesized by a simple and mild hyd ... r, vacuum filtration and drying at 60 degC in air."
2399,10.1007/s10854-014-2616-5,hydrothermal_ceramic_synthesis,"In this typical procedure of hydrothermal reaction ... clave, sealed and maintained at 180 degC for 24 h."
2400,10.1016/j.matlet.2014.04.137,hydrothermal_ceramic_synthesis,Synthesis of TiO2crystals: TiO2 crystals were synt ... th distilled water and dried at 80 degC overnight.
2401,10.1016/j.jpowsour.2006.09.094,hydrothermal_ceramic_synthesis,A nanostructured amorphous Co3Sn2 were prepared by ... or 2 h in flowing N2 to obtain crystalline Co3Sn2.
2402,10.1016/j.ijhydene.2014.01.029,hydrothermal_ceramic_synthesis,"First, titanium tetrabutoxide (3 ml) was drop wise ... white color powder was successfully prepared [13]."
2403,10.1016/j.jallcom.2011.06.100,hydrothermal_ceramic_synthesis,"ZnO was prepared by a simple hydrothermal reaction ... t last, the obtained product was dried at 60 degC."
2404,10.1016/j.cej.2017.01.054,hydrothermal_ceramic_synthesis,Pristine Zn0.5Cd0.5S nanoparticles were synthesize ... s then washed repeatedly with ethanol and acetone.
2405,10.1007/s10854-017-6631-1,hydrothermal_ceramic_synthesis,T-001 were synthesized via a simple hydrothermal m ... es and then dried overnight in an oven at 80 degC.
2406,10.1016/j.apcatb.2016.10.027,hydrothermal_ceramic_synthesis,"The KTaO3 semiconductor was prepared by the hydrot ...  for 8 h. Finally, some white powder was obtained."
2407,10.1007/s10854-015-3995-y,hydrothermal_ceramic_synthesis,"In a typical hydrothermal synthesis, 0.249 g Co(Ac ... 400 degC for 3 h in air to produce Co3O4 nanorods."
2408,10.1007/s10854-014-1917-z,hydrothermal_ceramic_synthesis,All the chemical reagents were of analytical grade ... with deionized water and dried at 80 degC for 4 h.
2409,10.1016/j.jpowsour.2009.01.028,hydrothermal_ceramic_synthesis,The (NH4)0.83Na0.43V4O10*0.26H2O nano-platelet clu ... ith deionized water and dried at 60 degC for 12 h.
2410,10.1016/j.jpowsour.2008.04.011,hydrothermal_ceramic_synthesis,All chemicals were of analytical grade and used wi ... g the heating process could be described as below:
2411,10.1016/j.nanoen.2015.10.036,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.14 g CoCl2*6H2O and 0.15 ... NSs was then rinsed and dried at 60 degC for 12 h."
2412,10.1016/j.matlet.2009.02.016,hydrothermal_ceramic_synthesis,"For the preparation of CdS nanowires, the prepared ... e yellow powder was obtained for characterization."
2413,10.1016/j.jssc.2005.10.024,hydrothermal_ceramic_synthesis,"In a typical hydrothermal post-treatment, 0.55 g o ... red and dried in a vacuum oven at 80 degC for 8 h."
2414,10.1016/j.apsusc.2017.01.244,hydrothermal_ceramic_synthesis,Graphite oxide(GO) was synthesized with a previous ... h to obtain novel hierarchical flowers-like Sn3O4.
2415,10.1016/j.nanoen.2016.02.051,hydrothermal_ceramic_synthesis,"MnO2 nanowire: In a typical procedure, 2 mmol of K ...  after naturally cooling down to room temperature."
2416,10.1016/j.ensm.2016.04.002,hydrothermal_ceramic_synthesis,"0.178 g of urea and 0.303 g of CoCl2*6H2O were dis ... oven at 80 degC for 10 h, yielding Co-CH nanorods."
2417,10.1016/j.molcata.2015.03.011,hydrothermal_ceramic_synthesis,"Method II: The BiPO4 was also prepared by a previo ... imes, and subsequently drying at 60 degC for 24 h."
2418,10.1016/j.apsusc.2016.04.175,hydrothermal_ceramic_synthesis,"Briefly, 2 mmol Co(CH3COO)2*4H2O was added into 40 ... C with a rising rate of 2 degC min for 2 h in air."
2419,10.1016/j.electacta.2014.10.105,hydrothermal_ceramic_synthesis,The Fe2O3/NCNT was synthesized using a hydrotherma ... llowed by calcination at 350 degCin air for 2.5 h.
2420,10.1016/j.materresbull.2013.09.030,hydrothermal_ceramic_synthesis,"Carbonaceous spheres were synthesized via a simple ...  for several times, and dried at 60 degC for 12 h."
2421,10.1016/j.matchemphys.2014.10.017,hydrothermal_ceramic_synthesis,All the chemical reagents used in this work were o ... ained precipitate was dried in an oven at 65 degC.
2422,10.1016/j.matlet.2008.11.032,hydrothermal_ceramic_synthesis,"In a typical synthesis, 1 g of cadmium sulphate (3 ... ater followed by ethanol and finally dried in air."
2423,10.1016/j.apcatb.2013.09.050,hydrothermal_ceramic_synthesis,BiPO4 and F-BiPO4 were synthesized via a hydrother ... ith distilled water and dried at 120 degC for 8 h.
2424,10.1016/j.matchemphys.2003.12.006,hydrothermal_ceramic_synthesis,The samples were prepared by hydrothermal method.  ... ried at 120 degC and calcined at 600 degC for 2 h.
2425,10.1016/j.matlet.2016.01.004,hydrothermal_ceramic_synthesis,All chemicals were analytical reagent and applied  ... t was dried in a vacuum oven at 120 degC for 24 h.
2426,10.1007/s11051-014-2250-4,hydrothermal_ceramic_synthesis,"In a typical synthesis of flower-like δ-MnO2, 0.97 ... ionized water, and then dried at 80 degC for 12 h."
2427,10.1007/s10853-015-8964-6,hydrothermal_ceramic_synthesis,"In a typical process, FeCl3*6H2O (0.675 g) and NaO ... nized water and ethanol for 3 times, respectively."
2428,10.1016/j.matlet.2014.02.042,hydrothermal_ceramic_synthesis,"In the following step, 0.03 g of the as obtained C ... on after being dried at 60 degC for 6 h in vacuum."
2429,10.1016/j.matchemphys.2004.05.027,hydrothermal_ceramic_synthesis,"All the analytical reagents used in this study wer ... es, and then dried in a vacuum at 50 degC for 6 h."
2430,10.1016/j.matlet.2006.01.034,hydrothermal_ceramic_synthesis,"All of the chemical reagents were of analytic-grad ... urities, and then dried at ambient air at 60 degC."
2431,10.1016/j.jpowsour.2011.10.067,hydrothermal_ceramic_synthesis,"All the reagents were used without further purific ... products obtained were named as S1, S2, S3 and S4."
2432,10.1007/s10854-015-3876-4,hydrothermal_ceramic_synthesis,"In a typical synthesis of SnO2 spheres, 0.267 g Na ... teel autoclave and maintained at 180 degC for 4 h."
2433,10.1016/j.optmat.2010.12.015,hydrothermal_ceramic_synthesis,"All chemicals were directly used as received witho ... ionized water, and then dried at 80 degC for 24 h."
2434,10.1016/j.matchemphys.2016.02.016,hydrothermal_ceramic_synthesis,The F-doped BiOCl samples were prepared via a simp ... thout addition of NaF was prepared for comparison.
2435,10.1016/j.jcis.2005.09.051,hydrothermal_ceramic_synthesis,"The samples were prepared by hydrothermal method i ... l times, and then dried in air at 60 degC for 4 h."
2436,10.1016/j.electacta.2016.02.202,hydrothermal_ceramic_synthesis,The OAM was synthesized according to the previousl ... 0 degC for 30 min to remove the residual organics.
2437,10.1016/j.jallcom.2015.11.023,hydrothermal_ceramic_synthesis,Polycrystalline Bi7F11O5 powder was synthesized by ... s collected with a yield of about 90% based on Bi.
2438,10.1016/j.electacta.2014.09.161,hydrothermal_ceramic_synthesis,α-MnO2 was prepared by a hydrothermal method [18]. ... . The as-synthesized MnO2 was denoted as sample C.
2439,10.1016/j.matchemphys.2005.09.057,hydrothermal_ceramic_synthesis,All the reagents were of analytical grade and were ... for 24 h and obtained with a subsequent treatment.
2440,10.1016/j.jallcom.2008.11.085,hydrothermal_ceramic_synthesis,"In a typical procedure for the solvothermal synthe ... and distilled water, then dried in air at 50 degC."
2441,10.1016/j.apsusc.2013.09.014,hydrothermal_ceramic_synthesis,All the reagents used here were analytically pure  ... xed and calcined in the air at 1000 degC for 18 h.
2442,10.1016/j.matlet.2015.03.099,hydrothermal_ceramic_synthesis,"All the chemical reagents were of analytical grade ...  several times, and then dried at 80 degC for 6 h."
2443,10.1016/j.apsusc.2015.03.100,hydrothermal_ceramic_synthesis,Uniform Bi2WO6 hierarchical microspheres were grow ... nd DI water and fully dried at 40 degC in an oven.
2444,10.1016/j.matlet.2014.05.178,hydrothermal_ceramic_synthesis,Synthesis of dual-phase Li4Ti5O12-TiO2nanoparticle ... ined in a tube furnace at 600 degC for 2 h in air.
2445,10.1016/j.matlet.2012.05.018,hydrothermal_ceramic_synthesis,"In a typical experiment, an appropriate amount of  ...  CS was then dried in a vacuum at 60 degC for 4 h."
2446,10.1016/j.jssc.2005.11.028,hydrothermal_ceramic_synthesis,"The reagents KMnO4 and CH3CH2OH are analytical gra ... ted after washing, filtering and drying in vacuum."
2447,10.1007/s00339-012-7333-4,hydrothermal_ceramic_synthesis,The Au NPs was decorated onto the surface of ZnO b ... d water and absolute ethanol and dried at 70 degC.
2448,10.1007/s10853-006-1309-8,hydrothermal_ceramic_synthesis,"In a typical synthesis process, 0.5 g C2Cl6, 5 g N ... ed water, then dried in vacuum at 60 degC for 2 h."
2449,10.1016/j.apcatb.2016.05.041,hydrothermal_ceramic_synthesis,MIL-53(Fe) was synthesized according to the litera ... ring and drying under vacuum at 100 degC for 10 h.
2450,10.1016/j.mseb.2008.09.049,hydrothermal_ceramic_synthesis,"The preparation procedure and the reagent quantity ... ted, to recover the product (YVO4:Dy3+ nanogrape)."
2451,10.1016/j.ssc.2005.05.002,hydrothermal_ceramic_synthesis,"All reagents were of 99.9% purity from Shanghai Ch ... imes each, and dried in vacuum at 50 degC for 4 h."
2452,10.1002/celc.201500033,hydrothermal_ceramic_synthesis,"At first, α-MnO2 was prepared by using a hydrother ... eat-treated at 400-1000 degC for a period of time."
2453,10.1016/j.jpcs.2014.05.011,hydrothermal_ceramic_synthesis,Different mass ratios C3N4-BiVO4 heterojunctions w ... the same conditions in the absence of C3N4 powder.
2454,10.1016/j.materresbull.2012.12.038,hydrothermal_ceramic_synthesis,The porous Fe3O4/g-C3N4 nanospheres were obtained  ... /g-C3N4-x (x denotes the Fe3O4/g-C3N4 mass ratio).
2455,10.1016/j.electacta.2014.07.095,hydrothermal_ceramic_synthesis,Amorphous ZnSnO3-C hollow microcubes were fabricat ... or 4 h with a heating rate of 1 degC/min in argon.
2456,10.1016/j.nanoen.2016.02.056,hydrothermal_ceramic_synthesis,"Typically, 30 mg Na2MoO4*2H2O and 60 mg C2H5NS wer ... fter centrifugation and dried at 80 degC for 12 h."
2457,10.1016/j.scriptamat.2015.08.009,hydrothermal_ceramic_synthesis,"For the synthesis of MgFe2O4 hollow spheres, 5 mmo ... and finally dried at 60 degC for characterization."
2458,10.1016/j.electacta.2015.04.018,hydrothermal_ceramic_synthesis,The (BiO)2CO3@MnO2 and Bi2O3@MnO2 nanostructures w ... imes and then dried at 60 degC for 6 h in an oven.
2459,10.1016/j.electacta.2015.10.023,hydrothermal_ceramic_synthesis,"For the synthesis of PSA-Fe3O4@C, 10 mmol FeCl2*4H ... as annealed in high-purity N2 at 500 degC for 8 h."
2460,10.1016/j.matlet.2006.11.050,hydrothermal_ceramic_synthesis,"All the reagents were of analytical grade and were ...  for several times, then dried at 70 degC for 1 h."
2461,10.1016/j.matlet.2013.04.010,hydrothermal_ceramic_synthesis,All chemicals are analytical grade and used as rec ... lly. The product of SnO2 nanoflowers was obtained.
2462,10.1016/j.ssi.2003.09.011,hydrothermal_ceramic_synthesis,"In a 50-ml Teflon vessel, 0.02 mol of analytically ... washed with ethanol and dried at 100 degC for 2 h."
2463,10.1016/j.electacta.2016.09.004,hydrothermal_ceramic_synthesis,α-MnO2 nanowires composite was synthesized by a si ...  and dried at 60 degC for 12 h in the vacuum oven.
2464,10.1016/j.matchemphys.2009.01.015,hydrothermal_ceramic_synthesis,"In a typical procedure for the solvothermal synthe ... and distilled water, then dried in air at 50 degC."
2465,10.1016/j.matlet.2013.09.081,hydrothermal_ceramic_synthesis,All the chemicals were analytical-grade reagents a ...  degC min-1 and then calcined at 450 degC for 2 h.
2466,10.1016/j.matchemphys.2009.01.014,hydrothermal_ceramic_synthesis,"All reagents were of AR grades and used without fu ... nd 11 were denoted as S1, S2 and S3, respectively."
2467,10.1016/j.electacta.2015.09.037,hydrothermal_ceramic_synthesis,All reagents are analytical grade without further  ... gC min-1 in air to obtain the black oxide powders.
2468,10.1016/j.jallcom.2008.06.008,hydrothermal_ceramic_synthesis,The synthesis of La2O3-Fe2O3 core-shell nanostruct ... final product and finally dried at 60 degC in air.
2469,10.1007/s10853-011-6241-x,hydrothermal_ceramic_synthesis,"Titanates were synthesized by a simple solvotherma ...  about 8, and dried in an infrared oven overnight."
2470,10.1016/j.carbon.2013.12.059,hydrothermal_ceramic_synthesis,"Typically, 1.677 g of tartaric acid was dissolved  ... lor of the product turned from pale blue to brown."
2471,10.1016/j.matlet.2011.10.062,hydrothermal_ceramic_synthesis,Y(NO3)3 and Eu(NO3)3 aqueous solutions were obtain ... ried and then calcined at 800 degC in air for 5 h.
2472,10.1016/j.ijhydene.2014.05.093,hydrothermal_ceramic_synthesis,"In a typical procedure, 3 mmol of NiCl2*6H2O and 6 ... 0 degC for 12 h. This sample was denoted as P-NFO."
2473,10.1016/j.jssc.2010.10.001,hydrothermal_ceramic_synthesis,The Fe3O4 nanoparticles were obtained by a polyol  ... ee times with ethanol and dried at 60 degC in air.
2474,10.1016/j.apcatb.2013.05.059,hydrothermal_ceramic_synthesis,"All chemicals were analytical-grade reagents and u ...  named as Z1, ZG75, ZG100, and ZG150 respectively."
2475,10.1016/j.matlet.2016.03.125,hydrothermal_ceramic_synthesis,Each of 5 mmol Bi(NO3)3*5H2O and Na2MoO6 was disso ... r the synthesis of heterostructure nanocomposites.
2476,10.1016/j.ijleo.2015.02.056,hydrothermal_ceramic_synthesis,The obtained mixture was transferred to a Teflon-l ...  distilled water and then dried in air at 80 degC.
2477,10.1016/j.jallcom.2015.06.204,hydrothermal_ceramic_synthesis,"A common hydrothermal method was employed to synth ... th deionized water, and dried at 80 degC for 12 h."
2478,10.1016/j.mseb.2016.03.010,hydrothermal_ceramic_synthesis,0.97 g Bi (NO3)3*5H2O was dissolved in a 10 mL CH3 ...  h. The Bi2WO6 photocatalyst was finally obtained.
2479,10.1016/j.jallcom.2016.01.189,hydrothermal_ceramic_synthesis,All the reagents are analytical grade and were use ... ucts were washed with deionized water and ethanol.
2480,10.1016/j.apsusc.2015.04.011,hydrothermal_ceramic_synthesis,"All the chemical reagents are analytically graded  ... e denoted as TQD-1, TQD-2 and TQD-3, respectively."
2481,10.1007/s10854-013-1397-6,hydrothermal_ceramic_synthesis,"ZnFe2O4 nanoparticles were synthesized by a typica ... um and final products were named as S2, S3 and S4."
2482,10.1016/j.jssc.2011.05.055,hydrothermal_ceramic_synthesis,All analytical chemicals were used without further ... d at 120 degC for 12 h and products were obtained.
2483,10.1016/j.jpowsour.2012.10.032,hydrothermal_ceramic_synthesis,Siliceous SBA-15 mesoporous material was synthesiz ... to remove the residual organic template materials.
2484,10.1016/j.cej.2016.06.100,hydrothermal_ceramic_synthesis,4 mmol Bi(NO3)3*5H2O was dissolved in 40 ml glycer ... nd dried at 80 degC for 12 h under air atmosphere.
2485,10.1016/j.matlet.2014.07.035,hydrothermal_ceramic_synthesis,Preparation of three different Fe3O4nanospheres: T ... acuum at room temperature before characterization.
2486,10.1016/j.matchemphys.2007.03.003,hydrothermal_ceramic_synthesis,"In a typical process, 1 mmol of different cobalt s ... ions for Co3O4 crystals are summarized in Table 1."
2487,10.1016/j.matlet.2015.10.117,hydrothermal_ceramic_synthesis,"All reagents used were of analytical purity and we ... y changing the reaction time (7, 12, 18 and 24 h)."
2488,10.1016/j.electacta.2013.08.154,hydrothermal_ceramic_synthesis,SnS2 nanoplates were synthesized from SnCl4*5H2O a ... S2 sample synthesized at 200 degC with pH of 10.5.
2489,10.1016/j.matchemphys.2012.07.013,hydrothermal_ceramic_synthesis,"All chemicals were analytic grade and used without ... or there times each, and dried at 80 degC for 6 h."
2490,10.1016/j.materresbull.2016.02.045,hydrothermal_ceramic_synthesis,Commercial anatase TiO2 powders (0.4 g) were put i ... on and dried at 60 degC for 12 h in a vacuum oven.
2491,10.1016/j.solidstatesciences.2011.07.008,hydrothermal_ceramic_synthesis,"Wafer-like BFO were synthesized via a hydrothermal ... l times, and then dried in vacuum oven at 70 degC."
2492,10.1016/j.materresbull.2015.11.017,hydrothermal_ceramic_synthesis,"All chemicals were analytical grade and were used  ... times, and dried in air at 60 degC for about 12 h."
2493,10.1016/j.cej.2011.10.059,hydrothermal_ceramic_synthesis,CuO particles were prepared using a CTAB-assisted  ... . A commercial CuO was used as reference catalyst.
2494,10.1016/j.matlet.2014.11.048,hydrothermal_ceramic_synthesis,"All used chemical reagents were of analytical grad ... ove unexpected ions, and drying at 60 degC in air."
2495,10.1016/j.apsusc.2017.01.223,hydrothermal_ceramic_synthesis,"70 mL of 0.5 M d-glucose monohydrate solution was  ... t 60 degC overnight, carbon spheres were obtained."
2496,10.1016/j.electacta.2014.12.026,hydrothermal_ceramic_synthesis,The precursor SnO2 NPs were synthesized by the hyd ... m freeze dried for 3 days to achieve the SnO2 NPs.
2497,10.1016/j.apcatb.2015.09.030,hydrothermal_ceramic_synthesis,BN/In2S3 composite was synthesized by a simple hyd ... he obtained products were dried in air at 60 degC.
2498,10.1016/j.electacta.2016.02.122,hydrothermal_ceramic_synthesis,"The N-NbO2 nanoparticles were prepared by further  ... , and then was dried for further characterization."
2499,10.1016/j.jssc.2012.05.016,hydrothermal_ceramic_synthesis,"All chemicals used in the present experiments were ...  ethanol several times, and then dried in the air."
2500,10.1016/j.matlet.2013.12.071,hydrothermal_ceramic_synthesis,Synthesis of TiO2 samples: the mesoporous TiO2 mic ... gC for 2 h in air to remove the residual organics.
2501,10.1016/j.cej.2014.06.095,hydrothermal_ceramic_synthesis,"First, 5.163 g of zinc nitrate was dissolved in 37 ... r 12 h. The obtained sample was labeled as ZIF-8C."
2502,10.1007/s10854-016-4854-1,hydrothermal_ceramic_synthesis,"In a typical preparation procedure, NiCl2*6H2O (1  ... ies and then dried in a vacuum at 60 degC for 6 h."
2503,10.1007/s10853-009-3367-1,hydrothermal_ceramic_synthesis,"In a typical synthesis process, 0.01 mol zinc acet ... lected for further characterization and treatment."
2504,10.1016/j.electacta.2011.07.033,hydrothermal_ceramic_synthesis,"In a typical reaction process, for the synthesis o ... ological, structural and compositional properties."
2505,10.1016/j.electacta.2015.09.080,hydrothermal_ceramic_synthesis,Fe2O3 was synthesized via a hydrothermal process.  ... degC in vacuum for 12 h to obtain Fe2O3 particles.
2506,10.1016/j.electacta.2012.11.103,hydrothermal_ceramic_synthesis,"All the chemicals were of analytical grade and use ... ingly are denoted as NiO-300, NiO-400 and NiO-500."
2507,10.1007/s10800-012-0393-5,hydrothermal_ceramic_synthesis,FeS2 powder was synthesized by a surfactant assist ... B is also obtained in the same way for comparison.
2508,10.1016/j.matlet.2013.03.103,hydrothermal_ceramic_synthesis,All reagents used were of analytical purity and we ...  degC min-1 and then calcined at 450 degC for 2 h.
2509,10.1016/j.ijhydene.2014.10.088,hydrothermal_ceramic_synthesis,"Similarly, α-MnO2 Nano-tubes were prepared by the  ... e product was dried at 60 degC for overnight [24]."
2510,10.1016/j.electacta.2013.11.181,hydrothermal_ceramic_synthesis,1.45 g of Co(NO3)2*6H2O and 1.4 g of HMT (hexameth ... he sample was annealed at 450 degC in air for 2 h.
2511,10.1016/j.carbon.2013.11.006,hydrothermal_ceramic_synthesis,The carbohydrates were mixed with 3.5 ml of distil ... d water and dried in an oven at 110 degC for 12 h.
2512,10.1007/s10854-016-5283-x,hydrothermal_ceramic_synthesis,All the chemicals were used as received without fu ... n an oven at 60 degC for 12 h to get dying powder.
2513,10.1002/smll.200700032,hydrothermal_ceramic_synthesis,All the chemicals were of analytical grade and use ...  washed with deionized water and dried at 55 degC.
2514,10.1016/j.cej.2012.01.016,hydrothermal_ceramic_synthesis,AF-Fe3O4 were prepared by the reported hydrotherma ... o AF-Fe3O4 is 0.1790 μg/mg by ninhydrin test [41].
2515,10.1016/j.apcatb.2013.04.019,hydrothermal_ceramic_synthesis,Bi2O2CO3/Bi2MoO6 composites were synthesized by a  ...  by deionized water and dried at 60 degC for 12 h.
2516,10.1016/j.jcrysgro.2004.04.093,hydrothermal_ceramic_synthesis,Hydrothermal method: All polycrystalline samples w ... th distilled water and dried in an oven at 80degC.
2517,10.1016/j.apcatb.2013.03.027,hydrothermal_ceramic_synthesis,"For synthesis of G(3 wt%)/ZnO, 0.64 g of zinc powd ... t%)/ZnO photocatalyst was dried at 60 degC in air."
2518,10.1016/j.mseb.2010.05.019,hydrothermal_ceramic_synthesis,All chemical reagents are of analytical grade and  ... uct was dried in vacuum at 60 degC for about 10 h.
2519,10.1007/s10854-006-0042-z,hydrothermal_ceramic_synthesis,NiFe2O4 nanoparticles were synthesized by the lite ... h distilled water and was dried for several hours.
2520,10.1016/j.cplett.2016.04.091,hydrothermal_ceramic_synthesis,"All of the reagents were analytical grade without  ... ol, and then dried in an oven at 60 degC for 12 h."
2521,10.1016/j.cej.2014.07.071,hydrothermal_ceramic_synthesis,NiFe2O4 nanoparticles were prepared using the hydr ...  samples were dried in vacuum at 80 degC for 12 h.
2522,10.1016/j.cej.2012.01.059,hydrothermal_ceramic_synthesis,"Ferrite with molar Fe3+/Fe2+ = 2 was prepared by m ... ater, and drying in the oven at 80 degC overnight."
2523,10.1016/j.solidstatesciences.2011.08.006,hydrothermal_ceramic_synthesis,"Two compounds were synthesized by hydrothermal met ... , H 3.52, N 10.88; found C 32.45, H 3.34, N 10.30."
2524,10.1016/j.matlet.2007.11.069,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.17 g of CuCl2*2H2O and 0 ... olute ethanol, dried at 60 degC for 5 h in vacuum."
2525,10.1007/s10008-012-1856-7,hydrothermal_ceramic_synthesis,All of the chemicals were of analytical grade and  ... o the formation of the final highly layered Co3O4.
2526,10.1016/j.jssc.2010.01.015,hydrothermal_ceramic_synthesis,"In this procedure, 2 mmol manganese acetate tetrah ... brown powders were collected for characterization."
2527,10.1016/j.matlet.2015.10.142,hydrothermal_ceramic_synthesis,"All chemicals (98% purity, analytical grade) were  ... obtained product was annealed at 800 degC for 4 h."
2528,10.1016/j.solidstatesciences.2012.12.009,hydrothermal_ceramic_synthesis,F-doped BiVO4 photocatalysts were fabricated using ...  the uncalcined olive-like porous BiVO4 precursor.
2529,10.1016/j.matlet.2012.07.109,hydrothermal_ceramic_synthesis,Certain amount of Bi(NO3)3*5H2O dissolved by 3.0 m ... were collected in the same way as collecting BiOI.
2530,10.1016/j.matlet.2012.02.080,hydrothermal_ceramic_synthesis,"Analytical grade KMnO4, PEG 400, and deionized wat ... es, subsequently dried at 60 degC for 12 h in air."
2531,10.1002/chem.201103523,hydrothermal_ceramic_synthesis,Synthesis of the TiO2 nanowires: All chemicals wer ... muffle furnace at 450 degC for 2 h (3 degC min-1).
2532,10.1016/j.apsusc.2012.04.006,hydrothermal_ceramic_synthesis,Hollow and spindle-shaped α-Fe2O3 was obtained via ... uct was dried in a vacuum box at 80 degC for 12 h.
2533,10.1016/j.snb.2016.05.142,hydrothermal_ceramic_synthesis,The porous FeVO4 nanorods were prepared according  ... n air at 500 degC for 2 h at a rate of 5 degC/min.
2534,10.1016/j.matchemphys.2009.02.030,hydrothermal_ceramic_synthesis,"In a typical synthesis process, 0.01 mol zinc acet ... lected for further characterization and treatment."
2535,10.1016/j.electacta.2010.12.033,hydrothermal_ceramic_synthesis,The carbon coating process was performed via a sub ...  LiTiOPO4 by substituting LiNO3 for Ni(NO3)2*6H2O.
2536,10.1016/j.cattod.2014.02.035,hydrothermal_ceramic_synthesis,RUB-36 and RUB-39 were interlayer expanded with (3 ... s were also performed with DCDMS instead of 3-MPS.
2537,10.1016/j.electacta.2013.04.023,hydrothermal_ceramic_synthesis,"Here, the preparation process of PbOHCl is similar ...  from Sinopharm Chemical Reagent Shanghai Co. Ltd."
2538,10.1016/j.matlet.2013.03.021,hydrothermal_ceramic_synthesis,Amorphous silica nanoparticles with the diameter o ...  was fired at 1300 degC for 8 h in air atmosphere.
2539,10.1016/j.optmat.2012.05.005,hydrothermal_ceramic_synthesis,The synthesis procedures of CdWO4 were as follows: ... thanol several times and dried at 80 degC for 6 h.
2540,10.1016/j.jssc.2014.06.031,hydrothermal_ceramic_synthesis,"VS4/rGO hybrids materials were synthesized by the  ... DI water, and dried at 60 degC for 10 h in vacuum."
2541,10.1016/j.electacta.2014.01.118,hydrothermal_ceramic_synthesis,MnOOH was prepared via hydrothermal treatment. 19  ... OH was obtained after drying at 80 degC in vacuum.
2542,10.1016/j.cej.2013.07.053,hydrothermal_ceramic_synthesis,"The hydrothermal-calcination method is adopted for ... ally, the powder was calcined at 450 degC for 3 h."
2543,10.1016/j.ssc.2009.02.002,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.001 mol of Co(NO3)2 and  ... by heating these precipitates at 300 [?]C for 3 h."
2544,10.1016/j.electacta.2014.10.140,hydrothermal_ceramic_synthesis,All the reagents used in the experiments were anal ... cursor well and then improve the sintering effect.
2545,10.1016/j.chroma.2015.09.044,hydrothermal_ceramic_synthesis,"The resulted solution, after complete reaction, wa ... es and then dried at 100 degC for 6 h in air [24]."
2546,10.1016/j.jssc.2015.09.025,hydrothermal_ceramic_synthesis,"The ZnInxS4+y samples were prepared by a hydrother ... +y (x=1.6, 2.0, 2.3, 2.6, 2.9, 3.1), respectively."
2547,10.1016/j.electacta.2014.04.007,hydrothermal_ceramic_synthesis,The preparation of MoS2 nanosheet was conducted by ... n a vacuum oven at 80 degC for 12 h. 0.30 g 0.80 g
2548,10.1016/j.jpowsour.2007.08.090,hydrothermal_ceramic_synthesis,The rutile TiO2 powders can be converted to anatas ... samples were dried in vacuum overnight at 80 degC.
2549,10.1016/j.jpowsour.2016.01.005,hydrothermal_ceramic_synthesis,LiV3O8 nanoflakes were prepared through the calcin ... in air to get the final product LiV3O8 nanoflakes.
2550,10.1007/s11837-015-1516-3,hydrothermal_ceramic_synthesis,"AgNO3 and Zn(NO3)2*6H2O with a total 2.5 mmol plus ... 4 and 5% Ag contents, respectively, were prepared."
2551,10.1016/j.matlet.2013.09.030,hydrothermal_ceramic_synthesis,All chemical reagents were of analytic purity and  ...  and dried in vacuum at 60 degC for more than 4 h.
2552,10.1016/j.jssc.2007.10.031,hydrothermal_ceramic_synthesis,"First, NH4VO3 (2 mmol) was dissolved in hot distil ... s, and then dried under vacuum at 60 degC for 6 h."
2553,10.1016/j.apsusc.2014.07.185,hydrothermal_ceramic_synthesis,"To obtain Bi2O2CO3 nanosheet samples, 1.5 mmol Bi( ...  times and then dried in oven at 80 degC for 12 h."
2554,10.1007/s10853-013-7277-x,hydrothermal_ceramic_synthesis,The ZnS:Ag nanoparticles were synthesized via a ty ... articles having a yellow-gray color were obtained.
2555,10.1016/j.solidstatesciences.2010.10.023,hydrothermal_ceramic_synthesis,All the reagents are of analytical purity grade an ...  500 degC for 5 h at a heating rate of 5 degC/min.
2556,10.1016/j.electacta.2015.12.135,hydrothermal_ceramic_synthesis,The porous TiO2 microspheres were prepared by a so ... ng the white precursor at 400 degC for 3 h in air.
2557,10.1016/j.jcrysgro.2009.10.027,hydrothermal_ceramic_synthesis,CuO-CeO2 nanowire precursors were synthesized by a ... ir for 2 h and straw green products were obtained.
2558,10.1016/j.materresbull.2012.08.045,hydrothermal_ceramic_synthesis,"All chemicals were analytical grade and were used  ... rature. As a result, yellow powders were obtained."
2559,10.1016/j.cej.2016.06.097,hydrothermal_ceramic_synthesis,Synthesis of 3D Co3O4@NiO NWs on Nickel Foam: In a ...  air for 3 h to get a hierarchical Co3O4@NiO NWAs.
2560,10.1016/j.matlet.2011.12.035,hydrothermal_ceramic_synthesis,All chemical reagents utilized in the present stud ... 00 degC for 1 h to obtain the light yellow powder.
2561,10.1016/j.matlet.2011.02.009,hydrothermal_ceramic_synthesis,"In a typical synthesis, a mixture of EuCl3[?] 6H2O ... bsolute alcohol (5 ml x 5), and then dried in air."
2562,10.1016/j.cej.2014.12.066,hydrothermal_ceramic_synthesis,"MnO2 nanorods and nanotubes were prepared by a hyd ... led as Mn-nanorods and Mn-nanotubes, respectively."
2563,10.1016/j.matdes.2015.10.121,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade and used as ... ral times, then dried in oven at 60 degC for 12 h."
2564,10.1016/j.solidstatesciences.2010.06.008,hydrothermal_ceramic_synthesis,All reagents are analytical reagents and used as r ... es were dried in a vacuum oven at 60 degC for 8 h.
2565,10.1002/zaac.200900273,hydrothermal_ceramic_synthesis,"(NiL)3Co(ClO4)2 (2): Complex 2 was prepared by a s ... u} = 3448 (br), 1638 (s), 1608 (m), 1092 (s) cm-1."
2566,10.1016/j.matdes.2016.06.034,hydrothermal_ceramic_synthesis,3.0 g CaSO4*2H2O was mixed with 60 mL distilled wa ...  calcinated at 800 degC for 4 h in muffle furnace.
2567,10.1016/j.apcatb.2012.04.009,hydrothermal_ceramic_synthesis,SnS2 photocatalyst was prepared by a hydrothermal  ... nt Corporation and used without further treatment.
2568,10.1007/s10854-015-2771-3,hydrothermal_ceramic_synthesis,"In this typical process of hydrothermal reaction,  ... led and maintained at 180 degC for 4 h at an oven."
2569,10.1016/j.molcata.2012.01.001,hydrothermal_ceramic_synthesis,TiO2 particles prepared according to the method de ...  according to this procedure was denoted as S4(X).
2570,10.1007/s10854-015-3087-z,hydrothermal_ceramic_synthesis,Ni microspheres were prepared with the solution re ... products were dried at 60 degC for 12 h in vacuum.
2571,10.1016/j.mssp.2014.06.051,hydrothermal_ceramic_synthesis,TNT was synthesized using the hydrothermal method. ... the prepared TNT was ground and sieved (200 mesh).
2572,10.1016/j.matchemphys.2008.07.058,hydrothermal_ceramic_synthesis,"All the reagents used were of analytical grade. In ... r several times, and then dried at 60 degC in air."
2573,10.1016/j.jallcom.2014.01.168,hydrothermal_ceramic_synthesis,The hydrothermal method was used to prepare TiO2 n ... cuum at 40 degC then calcined at 550 degC for 5 h.
2574,10.1016/j.elecom.2013.07.005,hydrothermal_ceramic_synthesis,The MnO2 nanobowls were synthesized by a hydrother ...  with deionized H2O and dried at 60 degC for 24 h.
2575,10.1016/j.matlet.2012.04.037,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade and used wi ... on, washed by ethanol, and dried under atmosphere."
2576,10.1016/j.materresbull.2009.12.016,hydrothermal_ceramic_synthesis,All the chemicals were analytic grade reagents wit ... ethanol several times and dried in air at 80 degC.
2577,10.1016/j.cej.2010.09.052,hydrothermal_ceramic_synthesis,"All chemicals (analytical grade) were purchased fr ... ute ethanol, and dried in air at room temperature."
2578,10.1016/j.mssp.2010.02.002,hydrothermal_ceramic_synthesis,"In a typical hydrothermal process [23], [24] and [ ... ater followed by ethanol and finally dried in air."
2579,10.1007/s10854-015-3607-x,hydrothermal_ceramic_synthesis,"ZnO nanoparticles were synthesized by a hydrotherm ... factant, the resultant sample was assigned as ZnO."
2580,10.1016/j.apcatb.2015.05.061,hydrothermal_ceramic_synthesis,Ag@C core-shell nanostructures were synthesized by ... g@C product was dried at 60 degC in air overnight.
2581,10.1016/j.electacta.2012.07.010,hydrothermal_ceramic_synthesis,"In a typical experiment, Ni(NO3)2*6H2O (0.004 mol) ... der the same conditions (denoted as Al-α-Ni(OH)2)."
2582,10.1002/chem.201405698,hydrothermal_ceramic_synthesis,"In a typical procedure, Mn(NO3)2[?]4 H2O (0.2 g) a ...  10 h to obtain the mesoporous flake-like MnCo2O4."
2583,10.1016/j.apsusc.2017.05.176,hydrothermal_ceramic_synthesis,A general procedure proceeded as follows. 2 g SnCl ... ning the defected SnO2 at 900 degC for 4 h in air.
2584,10.1016/j.snb.2011.04.050,hydrothermal_ceramic_synthesis,All the reagents in the experiment were analytical ... ining the precipitates at 600 degC for 2 h in air.
2585,10.1016/j.matlet.2013.01.001,hydrothermal_ceramic_synthesis,"Preparation of β-FeOOH nanorods: For the synthesis ... nd ethanol, and finally dried at 60 degC for 12 h."
2586,10.1016/j.matchemphys.2009.01.019,hydrothermal_ceramic_synthesis,NH4HF2 (50 mg) was first dissolved into 40 ml of a ... ed and washed several times with absolute ethanol.
2587,10.1016/j.electacta.2013.12.049,hydrothermal_ceramic_synthesis,LTO/Cu was prepared by hydrothermal method. 0.1010 ... e pure Li4Ti5O12 was prepared in a similar manner.
2588,10.1016/j.colsurfa.2015.01.002,hydrothermal_ceramic_synthesis,The magnetic Fe3O4 microsphere and magnetic core-s ... re was dried at 60 degC in a vacuum oven for 12 h.
2589,10.1016/j.matlet.2014.06.103,hydrothermal_ceramic_synthesis,"Synthesis: All the reagents used as received. In a ... y absolute ethanol, then dried at 60 degC for 8 h."
2590,10.1016/j.physb.2010.05.045,hydrothermal_ceramic_synthesis,A solution of Zn(AC)2 (2 mmol) and AlCl3 (2 mmol)  ... es were characterized by X-ray powder diffraction.
2591,10.1016/j.matlet.2015.09.079,hydrothermal_ceramic_synthesis,"The unique Ni-MOF samples were synthesized by a mo ... imes, and dried at 120 degC under vacuum for 12 h."
2592,10.1016/j.jssc.2007.11.010,hydrothermal_ceramic_synthesis,All the reagents were purchased from Shanghai Chem ...  dried in a vacuum desiccator at 80 degC for 12 h.
2593,10.1016/j.jcrysgro.2016.06.024,hydrothermal_ceramic_synthesis,Bismuth tri-iodide nanoparticles have been synthes ... ugation at 5000 rpm and dried at 60 degC for 24 h.
2594,10.1016/j.electacta.2016.05.085,hydrothermal_ceramic_synthesis,Cubic Co3O4 synthesis (a modified hydrothermal met ... egC for 10 h with a heating rate of 10 degC min-1.
2595,10.1016/j.materresbull.2012.06.002,hydrothermal_ceramic_synthesis,"The indium oxide nanostructures were synthesized b ... 0 degC) in a muffle furnace for 5 h, respectively."
2596,10.1016/j.mseb.2011.04.010,hydrothermal_ceramic_synthesis,"Typically, glucose (10.0 g) and Fe(NO3)3*9H2O (4.0 ... nd ethanol, and finally dried at 60 degC for 12 h."
2597,10.1016/j.optcom.2015.02.031,hydrothermal_ceramic_synthesis,The SnO2 nanoparticles were prepared by the hydrot ... ole products were annealed at 450 degC for 30 min.
2598,10.1016/j.matchemphys.2010.03.086,hydrothermal_ceramic_synthesis,"Typically, 2.1 g of Na2WO4 was dissolved in 30 mL  ...  then hydrothermally treated at 180 degC for 12 h."
2599,10.1016/j.jallcom.2007.01.142,hydrothermal_ceramic_synthesis,All chemicals used were analytical grade reagents  ... thanol three times and dried at 60 degC in vacuum.
2600,10.1007/s10854-013-1286-z,hydrothermal_ceramic_synthesis,"In a typical experiment, 0.3 mmol of cadmium chlor ... water several times to remove residual impurities."
2601,10.1016/j.jssc.2012.02.061,hydrothermal_ceramic_synthesis,"Preparation of MnCO3 dumbbells: 0.5 g of MnCl2*4H2 ... duct was collected, washed and dried under vacuum."
2602,10.1016/j.jpowsour.2014.12.153,hydrothermal_ceramic_synthesis,The Ni-foam@GNS@MnO2 composite was prepared by a h ...  The reaction process is assumed to be as follows:
2603,10.1016/j.jallcom.2014.05.041,hydrothermal_ceramic_synthesis,A surfactant solution was made by dissolving 0.091 ... degC for 12 h. The final powder was named as Mn-O.
2604,10.1016/j.matlet.2004.06.034,hydrothermal_ceramic_synthesis,"In a typical procedure, 3.0 ml SiCl4 and 7.5 g NaN ... 1.1 g white-grey powders were ultimately obtained."
2605,10.1007/s10800-014-0698-7,hydrothermal_ceramic_synthesis,All of the reactants and solvents were of analytic ... lcined at 800 degC for 5 h under an Ar atmosphere.
2606,10.1016/j.nanoen.2016.04.038,hydrothermal_ceramic_synthesis,"Three PTNTs with different porous texture were syn ... ned and designated as T1, T2 and T3, respectively."
2607,10.1016/j.matlet.2012.10.054,hydrothermal_ceramic_synthesis,"All reagents used in the experiments were of analy ...  Fe2O3, were also used to synthesize doped VO2(M)."
2608,10.1016/j.matlet.2012.10.066,hydrothermal_ceramic_synthesis,All the reagents were of analytical grade and used ... pitate was dried under vacuum at 50 degC for 24 h.
2609,10.1016/j.jpowsour.2013.11.016,hydrothermal_ceramic_synthesis,"All chemicals were analytical grade and used witho ... , and then dried in an oven at 120 degC overnight."
2610,10.1016/j.matlet.2017.01.130,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade, and used w ... t 60 degC overnight to acquire the final products."
2611,10.1016/j.matlet.2013.08.092,hydrothermal_ceramic_synthesis,All the chemical reagents were of analytical grade ... t 60 degC in vacuum for further characterizations.
2612,10.1016/j.apcata.2009.05.030,hydrothermal_ceramic_synthesis,"Ferric chloride hexahydrate (FeCl3*6H2O) was purch ... , and finally dried in an oven at 50 degC for 4 h."
2613,10.1016/j.matlet.2009.12.008,hydrothermal_ceramic_synthesis,"In a typical synthesis, 5 mmol KMnO4 and 5 mmol Cr ...  of HNO3. The final product was named as sample B."
2614,10.1007/s10854-016-5102-4,hydrothermal_ceramic_synthesis,All the reagents used in the present investigation ... t hydrothermal time to study the formation of ZnS.
2615,10.1016/j.electacta.2014.12.105,hydrothermal_ceramic_synthesis,"In this work, all chemicals are reagent grade and  ... orods have been transformed into α-Fe2O3 nanorods."
2616,10.1007/s10854-015-3803-8,hydrothermal_ceramic_synthesis,"The SnO2:Eu samples were synthesized by hydrotherm ... for a period of time (t = 1, 3 or 5 h) in the air."
2617,10.1007/s10854-015-3384-6,hydrothermal_ceramic_synthesis,"In this work, a BFO@CMS heterostructure was synthe ... s BFO@CMS5, BFO@CMS10 and BFO@CMS15, respectively."
2618,10.1016/j.jallcom.2016.01.092,hydrothermal_ceramic_synthesis,"ZnO NRs were prepared through a facile hydrotherma ... e ethanol, and dried in vacuum at 60 degC for 6 h."
2619,10.1007/s10854-015-3703-y,hydrothermal_ceramic_synthesis,GO nanosheets were prepared using modified Hummers ... ions were changed from yellowish brown into black.
2620,10.1016/j.solidstatesciences.2015.05.008,hydrothermal_ceramic_synthesis,"All chemicals were in analytic grade and used as r ... stilled water, and then dried at 80 degC for 10 h."
2621,10.1016/j.matlet.2008.09.001,hydrothermal_ceramic_synthesis,"All analytical chemicals were used without further ...  at 120 degC for 12 h, and products were obtained."
2622,10.1016/j.ijhydene.2014.10.088,hydrothermal_ceramic_synthesis,MnO2 Nano-particles were prepared by the following ... e product was dried at 60 degC for overnight [26].
2623,10.1016/j.conbuildmat.2016.05.082,hydrothermal_ceramic_synthesis,The hydrothermal method was used to synthesize Bi2 ... er of Bi2WO6 was finally dried at 70 degC for 8 h.
2624,10.1016/j.apsusc.2011.06.099,hydrothermal_ceramic_synthesis,"Hydrothermal method was employed in the synthesis  ... or 80 h in air, and was named S2 in the following."
2625,10.1016/j.electacta.2015.10.032,hydrothermal_ceramic_synthesis,The porous ZnMn2O4 nanowires were prepared though  ... 0 degC for 2 h to obtain porous ZnMn2O4 nanowires.
2626,10.1016/j.jpowsour.2014.03.043,hydrothermal_ceramic_synthesis,The CuO support was prepared by the hydrothermal m ... r 5 h and calcined at 400 degC for 4 h in the air.
2627,10.1002/asia.201402652,hydrothermal_ceramic_synthesis,"Typically, Ni(NO3)2[?]6 H2O (1 mmol) was added to  ...  at 300 degC for 2 h to obtain the final products."
2628,10.1016/j.matchemphys.2010.04.002,hydrothermal_ceramic_synthesis,"All regents were analytical grade and used without ... l for several times, then dried at 60 degC in air."
2629,10.1016/j.matlet.2011.10.002,hydrothermal_ceramic_synthesis,The CoNi submicrospheres were synthesized as follo ... finally dried in a vacuum oven at 60 degC for 8 h.
2630,10.1016/j.solmat.2015.11.025,hydrothermal_ceramic_synthesis,NiCo2O4 nanobelts were synthesized by a simple one ... gC min-1 in order to obtain the NiCo2O4 nanobelts.
2631,10.1016/j.jssc.2012.01.059,hydrothermal_ceramic_synthesis,In a typical experimental process of the synthesis ... d then dried in a vacuum oven at 80 degC for 12 h.
2632,10.1016/j.ica.2010.06.048,hydrothermal_ceramic_synthesis,"As in a typical solvothermal synthesis, 0.5 g zinc ... ally dried at 70 degC for 2 h in an electric oven."
2633,10.1016/j.matlet.2009.11.026,hydrothermal_ceramic_synthesis,The reactions were carried out in a Teflon-lined s ... and finally dried under vacuum at 60 degC for 6 h.
2634,10.1016/j.scriptamat.2007.04.034,hydrothermal_ceramic_synthesis,A simple mild procedure was used to synthesize mon ... oduct can be more than 70% under these conditions.
2635,10.1016/j.electacta.2014.08.085,hydrothermal_ceramic_synthesis,All the chemicals were analytical grade without fu ... tmosphere to obtain different Co3O4 nanoparticles.
2636,10.1002/chem.201101466,hydrothermal_ceramic_synthesis,Synthesis of TiO2 microspheres made up of nano-dec ...  (30 mL) were replaced by deionized water (60 mL).
2637,10.1016/j.mseb.2013.06.017,hydrothermal_ceramic_synthesis,Tin chloride pentahydrate (SnCl4*5H2O) (2.00 mmol) ... at 60 degC for 24 h for further characterizations.
2638,10.1007/s10854-016-5949-4,hydrothermal_ceramic_synthesis,"Typically, required quantity of HCl and deionized  ... ral times and dried at room temperature overnight."
2639,10.1016/j.matchemphys.2005.05.035,hydrothermal_ceramic_synthesis,"In a typical procedure, a mixture of 1 mmol Bi(NO3 ... product and finally dried at 80 degC under vacuum."
2640,10.1002/asia.201301419,hydrothermal_ceramic_synthesis,"The C dots were synthesized by a one-step hydrothe ... mperature, a yellow aqueous solution was obtained."
2641,10.1016/j.materresbull.2012.05.022,hydrothermal_ceramic_synthesis,"In a typical synthesis, SiO2 (0.12 g) and Ni(Ac)2* ... ion and washed with distilled water several times."
2642,10.1016/j.jpowsour.2015.01.048,hydrothermal_ceramic_synthesis,All chemicals were analytical grade and used witho ... O2 and hydrothermal reaction at 180 degC for 24 h.
2643,10.1016/j.matlet.2012.01.126,hydrothermal_ceramic_synthesis,"The SnO flowers assembled with nano-petals were su ... degC for 12 h, and collected for characterization."
2644,10.1002/cplu.201402434,hydrothermal_ceramic_synthesis,"Hollow BiVO4 microspheres were prepared through a  ... d water, and then dried in air at 90 degC for 4 h."
2645,10.1016/j.ijhydene.2013.03.039,hydrothermal_ceramic_synthesis,"CeO2 nanoparticles were synthesized by a solution- ... at 60 degC for 24 h, calcined at 350 degC for 4 h."
2646,10.1002/celc.201300124,hydrothermal_ceramic_synthesis,"The spherical precursor, Ni0.83Co0.10Mn0.07(OH)2,  ... tilled water, and oven-dried overnight at 70 degC."
2647,10.1016/j.apsusc.2014.06.018,hydrothermal_ceramic_synthesis,"Flower-like MoS2 were prepared by a routine hydrot ... ol, and then dried in an oven at 80 degC for 12 h."
2648,10.1016/j.ijhydene.2014.04.092,hydrothermal_ceramic_synthesis,"MoS2-RGO composite reduced by HHA was synthesized  ... olute ethanol, finally dried at 60 degC in vacuum."
2649,10.1016/j.apcatb.2006.06.022,hydrothermal_ceramic_synthesis,All chemicals in this study were reagent-grade and ...  other experimental conditions were kept the same.
2650,10.1016/j.cplett.2008.02.071,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.11 g of Zn(CH3COO)2 * 2H ...  ethanol, respectively, and then dried at 50 degC."
2651,10.1016/j.nanoen.2016.06.029,hydrothermal_ceramic_synthesis,"In a typical experiment, 2 mL Ti-isopropoxide was  ... m at 60 degC for further use and characterization."
2652,10.1016/j.cej.2014.07.041,hydrothermal_ceramic_synthesis,All reagents were of an analytical grade and used  ... anol and then dried in a vacuum at 60 oC for 10 h.
2653,10.1007/s10853-011-6048-9,hydrothermal_ceramic_synthesis,"In a typical procedure, 1 mmol Fe(CH3COO)2*4H2O, 2 ... was also prepared without the addition of glucose."
2654,10.1016/j.matlet.2015.08.123,hydrothermal_ceramic_synthesis,Single-crystal Ni(OH)2 nanosheets were prepared by ... ernight to obtain the light green Ni(OH)2 powders.
2655,10.1016/j.elecom.2007.08.007,hydrothermal_ceramic_synthesis,Synthesis of NiFe2O4 nanoparticles was carried out ... and finally dried at 80 degC for characterization.
2656,10.1016/j.materresbull.2006.11.013,hydrothermal_ceramic_synthesis,A typical synthesis procedure for β-MnO2 with tetr ... drothermal treatment temperature or reaction time.
2657,10.1016/j.electacta.2012.04.063,hydrothermal_ceramic_synthesis,Bi2S3 nanorods were synthesized by a simple single ... ol several times and dried in a vacuum at 50 degC.
2658,10.1002/aenm.201200008,hydrothermal_ceramic_synthesis,"Materials Preparation: The Ni-containing precursor ... s were prepared by the reported methods.22, 25, 32"
2659,10.1016/j.cej.2013.03.015,hydrothermal_ceramic_synthesis,A schematic diagram of the synthesis procedure is  ... nd in an agate mortar and kept in a sealed bottle.
2660,10.1016/j.matlet.2012.06.078,hydrothermal_ceramic_synthesis,A typical process for the preparation of WO3*0.33H ... nd then dried at 50 degC in air for several hours.
2661,10.1016/j.matchemphys.2015.07.062,hydrothermal_ceramic_synthesis,"CoFe2O4-hydrochar was fabricated by a wet-chemical ... that, the precipitate was dried at 80 degC in air."
2662,10.1016/j.jallcom.2015.05.204,hydrothermal_ceramic_synthesis,"To synthesize α-Fe2O3@C nanorings, 0.25 g of the a ...  precipitate at 400 degC for 2 h in N2 atmosphere."
2663,10.1007/s11837-013-0607-2,hydrothermal_ceramic_synthesis,"In the second category, 2 mmol of NH4Fe(SO4)2*12H2 ...  S-3, and the one with PVP was abbreviated as S-4."
2664,10.1016/j.matlet.2011.09.074,hydrothermal_ceramic_synthesis,The dandelion-like multi-branched Sb2S3 nanowire s ... d water and dried under vacuum at 80 degC for 2 h.
2665,10.1016/j.jcis.2016.02.013,hydrothermal_ceramic_synthesis,As-received 5 mL of TALH solution was dropped into ... X mL of hydrazine monohydrate used for synthesis).
2666,10.1016/j.tsf.2014.05.042,hydrothermal_ceramic_synthesis,LiCoO2 nanospheres were synthesized according to t ...  finally dried under vacuum at 100 degC overnight.
2667,10.1016/j.apsusc.2014.08.053,hydrothermal_ceramic_synthesis,"All of the reagents used were of analytical purity ... times, following to be dried at 80 degC overnight."
2668,10.1016/j.matlet.2016.07.007,hydrothermal_ceramic_synthesis,"All reagents were of analytical grade and used wit ...  and CH3CH2OH several times, and dried at 75 degC."
2669,10.1016/j.matlet.2012.03.054,hydrothermal_ceramic_synthesis,"In a typical experiment, certain amount of NaOH we ... ment parameters and results are showed in Table 1."
2670,10.1016/j.matchemphys.2008.07.101,hydrothermal_ceramic_synthesis,Na2TeO3 (0.6 mmol) and poly(vinyl pyrrolidone) (PV ... l times with distilled water and absolute ethanol.
2671,10.1016/j.jcis.2012.07.068,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.1 g PVP was dissolved in ... llected by centrifugation and washed with ethanol."
2672,10.1016/j.micromeso.2006.07.015,hydrothermal_ceramic_synthesis,First Al(OH)3 (Pfaltz & Bauer; 99%) and NaOH (Carl ...  water and finally dried at 100-101 degC for 10 h.
2673,10.1016/j.jallcom.2013.01.029,hydrothermal_ceramic_synthesis,"The Co-doped ZnO nanoparticles were prepared by us ... ents of x = 0.01, 0.02, 0.03, 0.05, 0.10 and 0.15."
2674,10.1016/j.tsf.2007.10.004,hydrothermal_ceramic_synthesis,CdIn2S4 powder was synthesized by a hydrothermal m ... was then washed with ethanol and dried at 70 degC.
2675,10.1016/j.matchemphys.2009.03.031,hydrothermal_ceramic_synthesis,"All reagents used in this work were of analytical  ... -d NBBO, where X is days of hydrothermal reaction."
2676,10.1016/j.jelechem.2015.04.040,hydrothermal_ceramic_synthesis,Pure Co3O4 was fabricated by a simple hydrothermal ...  process of the composite is depicted in Scheme 1.
2677,10.1016/j.jpowsour.2011.02.044,hydrothermal_ceramic_synthesis,"LFP samples with spindle-like microstructures were ... phere (200 mL min-1, 10 vol.% H2 and 90 vol.% N2)."
2678,10.1016/j.cattod.2016.04.043,hydrothermal_ceramic_synthesis,The Co-CuBi2O4 composite was prepared using a faci ... tead of 0.5 mmol of Co(NO3)2*6H2O and 25 mL of EG.
2679,10.1016/j.ssc.2005.03.002,hydrothermal_ceramic_synthesis,"In a typical process, 0.002 mol of KMnO4 and 0.003 ...  and then dried under a vacuum at 60 degC for 3 h."
2680,10.1016/j.matlet.2014.05.201,hydrothermal_ceramic_synthesis,"A mixture containing 0.01 mol of Ti(O-C4H9)4, 0.01 ... RT) to 100 degC, 130 degC, 160 degC, and 180 degC."
2681,10.1016/j.matchemphys.2010.12.030,hydrothermal_ceramic_synthesis,Cu2O/Cu nanoflowers were synthesized using Cu(NO3) ... ared at different conditions are shown in Table 1.
2682,10.1016/j.materresbull.2013.06.051,hydrothermal_ceramic_synthesis,"Flower-like ZnO was prepared by a hydrothermal pro ... 0 degC for 8 h, and flower-like ZnO were obtained."
2683,10.1002/ejic.201402878,hydrothermal_ceramic_synthesis,"Preparation of In2O3 Nanostructures: All chemicals ... several times, and then dried at 60 degC for 12 h."
2684,10.1016/j.materresbull.2010.12.030,hydrothermal_ceramic_synthesis,"The Bi2S3 hierarchical nanostructures were prepare ... distilled water, and finally dried in air for 6 h."
2685,10.1016/j.jcat.2013.11.007,hydrothermal_ceramic_synthesis,N-doped carbon spheres were synthesized by a hydro ...  and approximately 3.0 g of product was collected.
2686,10.1016/j.electacta.2016.05.072,hydrothermal_ceramic_synthesis,All the reagents were analytical purity and used w ... products were calcined at 450 degC for 4 h in air.
2687,10.1007/s10854-014-2264-9,hydrothermal_ceramic_synthesis,"In a typical hydrothermal process, SnCl2*2H2O (0.4 ... vernight. Thus SnO2 porous nanorods were obtained."
2688,10.1016/j.matlet.2013.04.051,hydrothermal_ceramic_synthesis,Sample preparation: SnS nanorods were synthesized  ... the impurities before drying at 90 degC overnight.
2689,10.1007/s10854-015-4250-2,hydrothermal_ceramic_synthesis,All the chemical reagents were of analytical grade ... final products were dried in a chamber at 70 degC.
2690,10.1016/j.jpowsour.2013.03.087,hydrothermal_ceramic_synthesis,All chemicals are of analytical grade and were use ... nd dried in a 120 degC vacuum desiccator for 24 h.
2691,10.1016/j.matlet.2015.10.067,hydrothermal_ceramic_synthesis,All chemical reagents were of analytic purity and  ... to stabilize the structure and sensing properties.
2692,10.1016/j.snb.2013.02.073,hydrothermal_ceramic_synthesis,"In a typical procedure, 5 mL of ethanolamine, 1 mm ... solute ethanol before drying at 80 degC overnight."
2693,10.1016/j.mseb.2007.03.007,hydrothermal_ceramic_synthesis,NiCl2*6H2O (0.1 mmol) was respectively put into tw ... duct was dried in a vacuum box at 60 degC for 4 h.
2694,10.1016/j.matlet.2015.05.172,hydrothermal_ceramic_synthesis,"In a typical synthesis, KMnO4 and NaNO2 reagents w ... tion the product was calcined at 400 degC for 4 h."
2695,10.1016/j.matlet.2007.06.031,hydrothermal_ceramic_synthesis,"In a typical procedure for the synthesis of CdO ho ... th water and ethanol, and dried in air at 50 degC."
2696,10.1016/j.actamat.2009.10.001,hydrothermal_ceramic_synthesis,The flower-shaped SnO2 nanostructures were prepare ... electrical furnace in air at 300-700 degC for 4 h.
2697,10.1016/j.jallcom.2015.12.066,hydrothermal_ceramic_synthesis,The synthesis of ZnO-coated MoS2 nanosheets were u ... on is that the molar ratio of MoS2 and ZnO is 2:1.
2698,10.1007/s10854-013-1107-4,hydrothermal_ceramic_synthesis,"Synthesis of net-like SnO2 structures: 0.45 g of S ... ral times, and finally dried at 60 degC overnight."
2699,10.1016/j.cej.2016.06.094,hydrothermal_ceramic_synthesis,A simple hydrothermal method was used to fabricate ... ducts were dried under vacuum at 80 degC for 12 h.
2700,10.1016/j.apsusc.2014.04.044,hydrothermal_ceramic_synthesis,The standard procedure for the synthesis of LuF3:E ...  and then collected and dried at 80 degC for 10 h.
2701,10.1016/j.jpowsour.2015.08.025,hydrothermal_ceramic_synthesis,The petal-like Co0.85Se nanosheets were synthesize ... esidue of reactants and dried at 60 degC for 24 h.
2702,10.1016/j.matlet.2013.11.108,hydrothermal_ceramic_synthesis,"All chemical reagents were of analytical grade and ... r 12 h. Finally, the white products were obtained."
2703,10.1007/s10854-017-6976-5,hydrothermal_ceramic_synthesis,Go was synthesized using a modified Hummers' metho ... o and placed at hydrothermal for 14 h in 120 degC.
2704,10.1016/j.electacta.2014.10.079,hydrothermal_ceramic_synthesis,The CuS/MWCNTs composites were prepared as follows ... mes and then dried in vacuum at 80 degC overnight.
2705,10.1002/ente.201500161,hydrothermal_ceramic_synthesis,"KX (0.002 mol) was dissolved into deionized water  ... inally, the products were dried at 80 degC in air."
2706,10.1016/j.jelechem.2015.06.005,hydrothermal_ceramic_synthesis,"The MoS2 nanocomposite was synthesized as follows: ... mes, and then dried in vacuum at 60 degC for 24 h."
2707,10.1007/s10854-016-5429-x,hydrothermal_ceramic_synthesis,The Ag@AgBr nanospheres were prepared by a facile  ...  under the same conditions without heat treatment.
2708,10.1007/s10854-015-2969-4,hydrothermal_ceramic_synthesis,"In a typical synthesis, 20 mg of as-prepared CuO p ... degC to obtain the CuO/MnO2 core-shell structures."
2709,10.1016/j.electacta.2010.08.091,hydrothermal_ceramic_synthesis,0.25-0.5 SnS nanobelts and 0.5-1 g glucose were di ... tube was allowed to cool down to room temperature.
2710,10.1016/j.jallcom.2010.12.152,hydrothermal_ceramic_synthesis,The B-doped TiO2 hybrid oxide was synthesized by o ... he same method only without the addition of H3BO3.
2711,10.1016/j.colsurfa.2008.10.014,hydrothermal_ceramic_synthesis,"In a typical synthesis, 1.0 g ZrOCl2*8H2O and 0.6  ... emperature for 3 h (refer to the calcined sample)."
2712,10.1016/j.electacta.2015.07.018,hydrothermal_ceramic_synthesis,LiMnPO4 nanocrystals were synthesized via a facile ... t. The final collected product was denoted as LMP.
2713,10.1016/j.matlet.2011.01.011,hydrothermal_ceramic_synthesis,All the reagents used for the preparation of the P ... nd finally dried in the vacuum at 60 degC for 6 h.
2714,10.1016/j.materresbull.2006.08.030,hydrothermal_ceramic_synthesis,"In a typical synthesis, 4.2 g zinc acetate and 50  ...  Then, the products were dried at 50 degC for 8 h."
2715,10.1016/j.optmat.2015.04.001,hydrothermal_ceramic_synthesis,The Fe3O4@C microspheres were synthesized through  ... O4@C were washed with deionized water for 3 times.
2716,10.1016/j.jallcom.2008.03.048,hydrothermal_ceramic_synthesis,"Fabrication of ZnS nanoclusters was achieved by th ... ater for several times, and then dried at 80 degC."
2717,10.1002/adma.201201139,hydrothermal_ceramic_synthesis,Synthesis of ZnO single-shelled hollow spheres (SH ... ed with distilled water and ethanol several times.
2718,10.1007/s11051-015-3060-z,hydrothermal_ceramic_synthesis,The typical synthesis process of the carbon-coated ... ried in air. This product was denoted as H-TiO2/C.
2719,10.1007/s10854-016-5045-9,hydrothermal_ceramic_synthesis,"In a typical preparation, Bi(NO3)3.5H2O (0.485 g)  ... d as BVO-T (the T here means truncate octahedron)."
2720,10.1016/j.jpowsour.2012.07.105,hydrothermal_ceramic_synthesis,Carbon spheres were synthesized by a previously re ... btain product was dried in air at 80 degC for 6 h.
2721,10.1007/s00339-014-8644-4,hydrothermal_ceramic_synthesis,"In a typical procedure, 0.2 g (1 mmol) of CuAc2*H2 ... . The samples were collected for characterization."
2722,10.1016/j.matlet.2006.06.067,hydrothermal_ceramic_synthesis,"In a typical procedure, 4.5 g CaC2 powders and 3.6 ... t 80 degC, black powders were ultimately obtained."
2723,10.1016/j.elecom.2008.07.043,hydrothermal_ceramic_synthesis,"All chemicals are commercially available and were  ...  water and acetone, and dried at 60 degC for 12 h."
2724,10.1016/j.matchar.2016.02.021,hydrothermal_ceramic_synthesis,All of the reactants are of analytical grade and u ... nd dried in the air atmosphere at 60 degC for 4 h.
2725,10.1016/j.jpowsour.2014.09.144,hydrothermal_ceramic_synthesis,"In the preparation of NiCo2S4, 0.195 mmol of Ni(AC ...  dried at 60 degC for 24 h to obtain the products."
2726,10.1016/j.jhazmat.2010.08.080,hydrothermal_ceramic_synthesis,"All chemicals were of analytical grade and were us ... ined in air at 400, 500, 600 and 800 degC for 2 h."
2727,10.1016/j.apcatb.2010.06.012,hydrothermal_ceramic_synthesis,"β-MnO2 and α-Mn2O3 catalysts were prepared by a re ... 0 degC for 4 h and 600 degC for 2 h, respectively."
2728,10.1016/j.nanoen.2016.06.025,hydrothermal_ceramic_synthesis,"Bi2O(OH)2SO4. In a typical procedure, an aqueous s ... er for several times and dried at 60 degC for 5 h."
2729,10.1002/ente.201600275,hydrothermal_ceramic_synthesis,"In a typical process, 1 mmoL of CoCl2[?]6 H2O, 2 m ... ecursors were calcined in air at 500 degC for 4 h."
2730,10.1016/j.ssc.2013.10.028,hydrothermal_ceramic_synthesis,"All reagents used in the experiments were of analy ... possible residues, and dried in vacuum at 75 degC."
2731,10.1016/j.cej.2016.06.120,hydrothermal_ceramic_synthesis,"In a typical synthesis, ammonium molybdate ((NH4)6 ... C@MoS2 nanospheres except for the addition of PVP."
2732,10.1016/j.matlet.2011.01.017,hydrothermal_ceramic_synthesis,"In a typical experimental procedure for the prepar ...  times. Finally, the product was dried at 60 degC."
2733,10.1016/j.jssc.2011.03.022,hydrothermal_ceramic_synthesis,AgGaS2 nanomaterials were synthesized in a mixed s ... nding results of AgGaS2 are summarized in Table 1.
2734,10.1016/j.jcrysgro.2006.05.052,hydrothermal_ceramic_synthesis,"A procedure for the synthesis of Ba1+xV6O16*nH2O s ... mes, and then dried in vacuum at 60 degC for 10 h."
2735,10.1016/j.matlet.2013.01.035,hydrothermal_ceramic_synthesis,The starting materials were of analytical grade an ... id (sample 3) were prepared by the same procedure.
2736,10.1016/j.electacta.2016.01.224,hydrothermal_ceramic_synthesis,The titanium glycolate precursor spheres were synt ... everal times and dried at 70 degC for further use.
2737,10.1016/j.mssp.2016.05.016,hydrothermal_ceramic_synthesis,All the analytic grade reagents were used without  ...  and dried at 60 degC overnight to achieve powder.
2738,10.1016/j.matchemphys.2013.06.046,hydrothermal_ceramic_synthesis,"To obtain Bi2O2CO3 powders, 2.0 mmol of bismuth ni ...  water several times and dried at 60 degC for 6 h."
2739,10.1016/j.cplett.2016.03.037,hydrothermal_ceramic_synthesis,The Ni0.85Se nanosheets were synthesized by a hydr ...  drying precipitate in vacuum at 60 degC for 24 h.
2740,10.1016/j.matchemphys.2011.01.032,hydrothermal_ceramic_synthesis,Alkali hydrothermal method was used for the prepar ... e was finally calcined at 500 degC for 2 h in air.
2741,10.1016/j.jcrysgro.2005.06.051,hydrothermal_ceramic_synthesis,"In a typical solvothermal synthesis procedure, 0.4 ... d ethanol several times, and finally dried in air."
2742,10.1016/j.mseb.2005.02.065,hydrothermal_ceramic_synthesis,"In a typical experiment, all the reagents were ana ... y, the precipitates were dried at 50 degC for 5 h."
2743,10.1016/j.matlet.2014.03.103,hydrothermal_ceramic_synthesis,Preparation of ZnS solid microspheres: Hydrotherma ... m at 40 degC for 4 h for further characterization.
2744,10.1016/j.matchemphys.2013.06.043,hydrothermal_ceramic_synthesis,The template (carbon microspheres) was prepared vi ... es and dried at 70 degC for 24 h in a vacuum oven.
2745,10.1016/j.matlet.2016.03.027,hydrothermal_ceramic_synthesis,The experimental procedure was designed as follows ... another MoS2 sample was also prepared without PQA.
2746,10.1016/j.apsusc.2015.02.008,hydrothermal_ceramic_synthesis,Bare STO and MSTO nanocubes were synthesized by a  ... d totally the same in the absence of Mn(Cl)2*4H2O.
2747,10.1007/s10854-016-5726-4,hydrothermal_ceramic_synthesis,The ZnO nanostructures were obtained by a hydrothe ... e samples at 500 degC in a muffle furnace for 4 h.
2748,10.1016/j.jpowsour.2011.08.085,hydrothermal_ceramic_synthesis,Co2SnO4@C core-shell nanostructures were prepared  ... or 3 h under N2 at a ramping rate of 5 degC min-1.
2749,10.1007/s10854-014-1812-7,hydrothermal_ceramic_synthesis,"All the chemical reagents were of analytical grade ... Eu3+, BiPO4:2 %Sm3+, and BiPO4:(5 %Eu3+, 2 %Sm3+)."
2750,10.1007/s11837-014-0983-2,hydrothermal_ceramic_synthesis,A total of 2.5 mmol of Co(NO3)2*6H2O and 10.0 mmol ... es were the same as the ones used in preparing S2.
2751,10.1016/j.snb.2015.03.042,hydrothermal_ceramic_synthesis,"In a typical procedure, firstly, 5 mmol of SnSO4 a ... 500 degC for 2 h to obtain the pure SnO2 products."
2752,10.1016/j.jpowsour.2013.07.044,hydrothermal_ceramic_synthesis,"Typically, 6.834 ml tetrabutyl orthotitanate was f ... ples were denoted HTZ1, HTZ2, HTZ3, HTZ5 and HTZ7."
2753,10.1016/j.powtec.2011.11.040,hydrothermal_ceramic_synthesis,"All chemicals are analytical reagents and used as  ... cursor at 350 degC, 450 degC and 550 degC for 2 h."
2754,10.1016/j.matchemphys.2010.06.008,hydrothermal_ceramic_synthesis,"In a typical synthesis, 5 mmol KMnO4 and 7.5 mmol  ... ogy of the obtained product was also investigated."
2755,10.1016/j.solidstatesciences.2004.10.043,hydrothermal_ceramic_synthesis,Compound 2 was synthesized by hydrothermal method  ...  ambient temperature (48% yield based on cadmium).
2756,10.1016/j.matlet.2013.11.082,hydrothermal_ceramic_synthesis,Analytical Sm(NO3)3*6H2O and diethylenetriamine (D ... ly dried in vacuum drying oven at 60 degC for 3 h.
2757,10.1016/j.materresbull.2014.10.020,hydrothermal_ceramic_synthesis,All of the chemicals used in this paper were analy ... products were annealed at 800 degC for 2 h in air.
2758,10.1016/j.electacta.2014.10.022,hydrothermal_ceramic_synthesis,The scheme of γ-Fe2O3/KB composite forming mechani ... trate precursor powder at 320 degC in air for 1 h.
2759,10.1016/j.jpcs.2009.11.016,hydrothermal_ceramic_synthesis,"In a typical procedure, 6.7 g KMnO4 and 4.2 mL con ... pitated MnO2 was vacuum-dried at 80 degC for 12 h."
2760,10.1016/j.nanoen.2013.07.010,hydrothermal_ceramic_synthesis,"For the synthesis of NCQDs/TiO2, in a typical proc ... d and NCQDs were replaced with CQDs, respectively."
2761,10.1016/j.solidstatesciences.2009.04.014,hydrothermal_ceramic_synthesis,"In a typical synthetic procedure, stoichiometric a ...  and ethanol then dried at 50 degC for 6 h in air."
2762,10.1016/j.jcrysgro.2005.05.048,hydrothermal_ceramic_synthesis,"In a typical experiment, all reagents were analyti ... y, the precipitates were dried at 50 degC for 5 h."
2763,10.1016/j.matchemphys.2005.09.056,hydrothermal_ceramic_synthesis,"Details of a typical experiment are as follows: Cu ... imes, and then dried in vacuum at 60 degC for 4 h."
2764,10.1016/j.optmat.2014.10.026,hydrothermal_ceramic_synthesis,"In a typical procedure, 1.0 g CTAB and 1.5 mL of n ... ny acid or base, different morphologies will form."
2765,10.1016/j.colsurfa.2011.12.039,hydrothermal_ceramic_synthesis,"In a typical process, 0.18 g PSS and 2.12 g Zn(NO3 ... 0 degC in an oven for subsequent characterization."
2766,10.1016/j.matdes.2016.06.031,hydrothermal_ceramic_synthesis,Simple solvothermal method was used for the synthe ... red for further characterizations and application.
2767,10.1002/smll.201302879,hydrothermal_ceramic_synthesis,"Synthesis of MoS2 Nanosheets: sodium molybdate (Na ... ater, and freeze dried for subsequent experiments."
2768,10.1016/j.matlet.2014.12.137,hydrothermal_ceramic_synthesis,All chemicals used were analytic grade reagents an ... wer was also prepared without the addition of PVP.
2769,10.1016/j.powtec.2015.01.002,hydrothermal_ceramic_synthesis,"Ni/NiO nanocomposites were prepared by hydrotherma ... ein after referred as N3, N4 and N5, respectively."
2770,10.1016/j.jpowsour.2015.03.078,hydrothermal_ceramic_synthesis,"In a typical synthesis process, 0.75 g (2.8 mmol)  ...  through one-plot calcination at 600 degC for 2 h."
2771,10.1016/j.matlet.2015.09.126,hydrothermal_ceramic_synthesis,"The detailed synthesis procedure is described belo ...  similar route without adding 1,10-phenanthroline."
2772,10.1016/j.poly.2011.11.054,hydrothermal_ceramic_synthesis,"In a typical procedure, Ni(NO3)2.6H2O (1 mmol), et ... ction parameters unchanged (Table 1 and Scheme 1)."
2773,10.1016/j.matlet.2015.06.085,hydrothermal_ceramic_synthesis,All chemicals used were analytic grade reagents an ...  was obtained after annealing at 600 degC for 2 h.
2774,10.1016/j.materresbull.2012.07.002,hydrothermal_ceramic_synthesis,"All reagents were analytical-grade reagents and us ...  12 h, and finally collected for characterization."
2775,10.1016/j.nanoen.2015.10.036,hydrothermal_ceramic_synthesis,The pristine Co3O4 NCs were synthesized on nickel  ... ng at 200 degC in air for 1 h to obtain Co3O4 NCs.
2776,10.1016/j.snb.2015.01.130,hydrothermal_ceramic_synthesis,"α-Fe2O3 nanotubes used in the work were synthesize ... solute ethanol, and dried under vacuum at 60 degC."
2777,10.1016/j.electacta.2016.06.046,hydrothermal_ceramic_synthesis,"A precursor hybrid was prepared by one-step hydrot ... led as LTO-500, LTO-600 and LTO-700, respectively."
2778,10.1016/j.fuel.2015.02.002,hydrothermal_ceramic_synthesis,"Carbon nanospheres were prepared by simple, and st ... r and alcohol by four times cycling in centrifuge."
2779,10.1016/j.electacta.2015.06.138,hydrothermal_ceramic_synthesis,The MoSe2/rGO hybrid was synthesized by a simultan ... o prepared under the same experimental conditions.
2780,10.1007/s10853-012-6751-1,hydrothermal_ceramic_synthesis,All chemical reagents used in this study were of a ...  times and dried in an electrical oven at 80 degC.
2781,10.1016/j.jpowsour.2015.03.107,hydrothermal_ceramic_synthesis,All the materials were used as received without an ... r 2 h to obtain the final product of Ni-Mn oxides.
2782,10.1016/j.powtec.2012.05.007,hydrothermal_ceramic_synthesis,"0.5 g of CuCO3*Cu(OH)2 powder was weighted into a  ...  water and ethanol, and dried at 80 degC for 12 h."
2783,10.1016/j.apsusc.2009.01.056,hydrothermal_ceramic_synthesis,"NCS were prepared by a modified hydrothermal synth ...  ethanol, and finally dried at 40 degC in an oven."
2784,10.1016/j.physe.2012.02.016,hydrothermal_ceramic_synthesis,Analytical pure grade chemicals were used without  ... d by ethanol and finally dried at 70 degC for 2 h.
2785,10.1016/j.jpowsour.2010.04.088,hydrothermal_ceramic_synthesis,"S-Co(OH)2 is prepared via a facile co-precipitatio ... nized water at 50 degC, and labeled as sample (b)."
2786,10.1016/j.electacta.2013.06.149,hydrothermal_ceramic_synthesis,N atoms were doped into TiO2NTs by a facile hydrot ... utoclave was cooled to room temperature naturally.
2787,10.1016/j.matlet.2015.12.099,hydrothermal_ceramic_synthesis,2.5 mmol KMnO4 and 1 mL concentrated HCl were mixe ... as-synthesized samples were then dried in 60 degC.
2788,10.1016/j.matchemphys.2008.03.001,hydrothermal_ceramic_synthesis,"In a typical synthesis, 0.6 g Co(Ac)2*4H2O and 3.3 ... en dried in vacuum exsiccator at room temperature."
2789,10.1016/j.jallcom.2013.01.120,hydrothermal_ceramic_synthesis,Analytical grade l-arginine and CoSO4*7H2O were us ... h in air to obtain the final product of Co3O4 HMs.
2790,10.1016/j.apsusc.2014.07.158,hydrothermal_ceramic_synthesis,The CuCr2O4 samples were synthesized by hydrotherm ... ferent temperatures (500-800 degC) for 4 h in air.
2791,10.1016/j.matlet.2016.03.122,hydrothermal_ceramic_synthesis,The SnS2 sample was synthesized simply by a direct ... d then was dried at 60 degC to obtain the product.
2792,10.1016/j.jallcom.2015.12.177,hydrothermal_ceramic_synthesis,Bismuth nickelate nanorods were synthesized by the ...  bismuth nickelate nanorods powders were obtained.
2793,10.1016/j.carbon.2014.06.039,something_else,"Reduced graphene oxide/Mn3O4 (rGO/Mn3O4) nanocompo ... edures, and cheap MnSO4 is used as a Mn3O4 source."
2794,10.1016/j.jelechem.2006.05.014,something_else,"Compound 3: To 0.33 mL (2.7 mmol) of 1,4-butanedit ... m ether 1:2 v/v) to give 0.1 g (44%) of product 3."
2795,10.1016/j.jelechem.2006.05.014,something_else,"All solvents (SDS, France) and deuterated solvents ... ectrospray mode using a Branford Analytica source."
2796,10.1016/j.jcat.2013.08.019,something_else,Particular attention must be given to the possible ...  was found to be below the detection limit of XPS.
2797,10.1016/j.jcat.2013.08.019,something_else,TPD experiments were performed in the preparation  ... g the mass spectrometer signal for each component.
2798,10.1016/j.jcat.2013.08.019,something_else,The sample was prepared by forming mass-selected R ... 6]. The cleanliness was checked using ISS and XPS.
2799,10.1016/j.tsf.2015.01.035,something_else,"The In2Se3 films of 1 μm thickness were deposited  ... were kept at 1010 degC and 285 degC, respectively."
2800,10.1016/j.tsf.2015.01.035,something_else,The In2Se3 layers were deposited by CSP on molybde ... se parameters yield films of about 1 μm thickness.
2801,10.1016/j.actamat.2008.06.010,something_else,Analytical solutions are only available for the se ... composition with a matrix correction program [28].
2802,10.1016/j.cej.2007.11.013,something_else,Operation condition: 1 atm; 298 K; inlet gas mixtu ... 5 mg; the average density of the beds: 105 mg/cm3.
2803,10.1016/j.cej.2007.11.013,something_else,"The desulfurization experiment was carried out at  ... , the breakthrough time, and the mass of material."
2804,10.1016/j.cej.2007.11.013,something_else,A 0.4 g of dry material was added to 20 ml of deio ... gerScan 3.21 software provided by RBD Enterprises.
2805,10.1016/j.electacta.2007.02.024,something_else,The artificial patina was prepared in an aqueous a ... procedure for the patina formation was as follows:
2806,10.1016/j.electacta.2007.02.024,something_else,A bronze plate of 0.5 mm in thickness was cut into ... s then embedded into the epoxy resin quoted above.
2807,10.1016/j.tetlet.2014.06.060,something_else,Salicylic and anthranilic acid derivatives were us ... NaH/H2O or by using the system LiOH/H2O2/Na2SO3.11
2808,10.1016/j.apenergy.2015.11.011,something_else,"Pick stochastic particles to be penetrated by the  ... domly from the bulk zone, until their total volume"
2809,10.1016/j.jelechem.2006.05.014,something_else,Compound 4: In a 250 mL three-necked round bottom  ...  2:5 v/v) to give 45 mg of 4 as a red solid (40%).
2810,10.1016/j.jelechem.2006.05.014,something_else,3-Chloro-6-methoxy-s-tetrazine (2.7 mmol) (synthes ... te-petroleum ether 1/1 v/v) in 27% yield (0.15 g).
2811,10.1016/j.jelechem.2006.05.014,something_else,"3,6-Dichloro-s-tetrazine (6.6 mmol) is solubilised ... ount of monosubstituted compound is also isolated."
2812,10.1016/j.micromeso.2005.06.042,something_else,"RuCl3 * xH2O, 3-aminopropyltrimethoxy silane (APTS ... n the hydrothermal syntheses of MCM-41 and MCM-48."
2813,10.1016/j.jmatprotec.2006.07.022,something_else,"Effects of particle size, polishing pad and contact pressure in free abrasive polishing"
2814,10.1016/j.jmatprotec.2006.07.022,something_else,Deformation of pad subjected to single dresser can ... ion of polishing pad at time t can be expressed as
2815,10.1016/j.gca.2013.02.007,something_else,The yield of Cu(II) extraction by crown ethers has ... ce attributable to the equilibrium isotope effect.
2816,10.1016/j.gca.2013.02.007,something_else,Organic impurities carried over from the extractio ... rent analytical sessions is 0.10%0 (2σ) for δ65Cu.
2817,10.1016/j.gca.2013.02.007,something_else,CuCl2*2H2O was dissolved in HCl to prepare solutio ...  these solutions were saved for isotopic analysis.
2818,10.1016/j.gca.2013.02.007,something_else,"Dicyclohexano-18-crown-6 (DC18C6) (>97% purity) is ... cal, Co., Inc. Other chemicals were reagent grade."
2819,10.1016/j.solidstatesciences.2014.03.008,something_else,"In this kinetic study, OFW and KAS equations (mode ... calculations) were used to determine the Eα and A:"
2820,10.1016/j.cemconres.2016.06.001,something_else,Portions of each dried exhaustively leached C-S-H  ... sis for the modelling work described in Section 4.
2821,10.1016/j.apenergy.2015.11.011,something_else,Spray impingement and wall film evaporation models are added to SRM Engine Suite.
2822,10.1016/j.cemconres.2016.06.001,something_else,"On completion of the leaching studies, samples of  ... -atmosphere glovebox, as described in Section 2.1."
2823,10.1016/j.cemconres.2016.06.001,something_else,"For the leaching experiments, a target solid to li ...  controlled water bath maintained at 25 +- 1 degC."
2824,10.1016/j.cemconres.2016.06.001,something_else,"After curing, a number of portions of each (well-m ... emperature to determine their bound water content."
2825,10.1016/j.cemconres.2016.06.001,something_else,Compositions of synthetic low C/S C-S-H gels with  ... ven drying at 105 degC and drying over silica gel.
2826,10.1016/j.cemconres.2016.06.001,something_else,"C-S-H gels of low C/S were prepared by methods sim ... d gels were calculated, and are listed in Table 1."
2827,10.1016/j.micromeso.2005.06.042,something_else,"The catalysts were filtered from hot reaction mixt ... -propanol and DCM, and thereafter analyzed by XPS."
2828,10.1016/j.micromeso.2005.06.042,something_else,"The surfaces of amorphous (fumed) silica were modi ... ted as RuP-NH2-SiO2 and RuP-EN-SiO2, respectively."
2829,10.1016/j.micromeso.2005.06.042,something_else,"The RuCl2(PPh3)3 complex was synthesized applying  ... P-NH2-MCM-41/48 or RuP-EN-MCM-41/48, respectively."
2830,10.1016/j.micromeso.2005.06.042,something_else,"The calcined MCM-41 or MCM-48 materials were first ... ed as NH2-MCM-41/48 or EN-MCM-41/48, respectively."
2831,10.1016/j.cemconres.2016.06.001,something_else,"After a minimum of 11 days (and typically around 2 ... roup Ltd. (formerly Scientifics Ltd.), at Harwell."
2832,10.1016/j.apcata.2007.06.018,something_else,The catalytic measurements were carried out in a f ... ] and described in a previous study [8] were used.
2833,10.1016/j.apcata.2007.06.018,something_else,The surface areas of the carbon nanotubes and the  ... talysts with high and low metal loadings was made.
2834,10.1016/j.apcata.2007.06.018,something_else,A JEOL 2010F scanning transmission electron micros ... o standard procedures as described previously [8].
2835,10.1016/j.jeurceramsoc.2010.11.002,something_else,A monolithic material of monophase alumina and one ... ball milled with alumina jar and balls during 4 h.
2836,10.1007/s00339-013-7673-8,something_else,We investigated thin-film fs-laser doping using a  ... n the surface morphology and dopant incorporation.
2837,10.1016/j.optmat.2012.11.015,something_else,400 ml saturated of 5 mol% of glycine added KDP wa ...  cut and polished ingots are shown in the Fig. 2d.
2838,10.1016/j.optmat.2012.11.015,something_else,The SR method was employed using controllable ring ... rmometer shows the temperature near the seed [28].
2839,10.1016/j.optmat.2012.11.015,something_else,The commercially available KDP was used for the gr ... th methods we have chosen 5% of glycine added KDP.
2840,10.1016/j.optmat.2012.11.015,something_else,Solubility studies were carried out in a Constant  ... stivity of the used deionized water is 18.2 MΩ cm.
2841,10.1016/j.matchemphys.2016.05.034,something_else,"After the crystallization study, the resulting sam ... r 5 min and cooled down to 30 degC at 20 degC/min."
2842,10.1002/anie.201409252,something_else,[a] Reaction conditions: 1 (1.5 mmol); Ti(OiPr)4 ( ... . [g] Catalyst loading: 8 mol % of each component.
2843,10.1016/j.jeurceramsoc.2010.11.002,something_else,Monolithic and layered plates ([?]70 mm x 70 mm x  ... -1 and with 4 h dwell at 1200 degC during heating.
2844,10.1002/anie.201409252,something_else,[a] Reaction conditions: 1 a (1.5 mmol); Ti(OiPr)4 ... ng an internal standard. [c] 50 min reaction time.
2845,10.1002/app.25822,something_else,Particle size was measured by a laser light scatte ... corded and these results are included in Table II.
2846,10.1002/app.25822,something_else,Fourier transform infrared (FTIR) spectra of the p ...  the pellets by applying a pressure of 600 kg/cm2.
2847,10.1002/app.25822,something_else,Molecular weights of the synthesized PUs were dete ... t and polydispersity index are given in Table III.
2848,10.1002/app.25822,something_else,Weighed amounts of drug-loaded microspheres (10 mg ... acing the samples with a fresh dissolution medium.
2849,10.1002/app.25822,something_else,Microspheres of mPEG-grafted PU containing hydroph ... ance) to obtain the completely dried microspheres.
2850,10.1002/app.25822,something_else,Moderate molecular-weight block PUs were obtained  ... mers used for PU preparation are given in Table I.
2851,10.1002/app.25822,something_else,TMP and triethyl amine (1 : 1.1) were taken in a d ... o the formation of LA-TMP is shown in Scheme 1(b).
2852,10.1002/app.25822,something_else,Sebacoyl chloride was taken in a dry round bottom  ... e preparation of mPEG-TMP is shown in Scheme 1(a).
2853,10.1002/anie.201409252,something_else,"The results imply that the in situ generation of t ... tivity, but similar selectivity like L1 (entry 5)."
2854,10.1016/j.jcat.2008.10.016,something_else,The BaO/γ-Al2O3 NOx storage materials with varying ... 2200 FEF aberration corrected electron microscope.
2855,10.1016/j.jeurceramsoc.2010.11.002,something_else,Sliding wear tests were conducted on square sample ... nsidered for the friction coefficient calculation.
2856,10.1016/j.apcata.2007.06.018,something_else,"Keeping the Fe:Ru molar ratio the same, at 7.24, t ... 25Ru) was also synthesized by the same procedures."
2857,10.1016/j.apcata.2007.06.018,something_else,The carbon products of twelve CNT synthesis reacti ... dded drop-wise to 10 g of carbon nanotube support.
2858,10.1016/j.apcata.2007.06.018,something_else,CNTs were synthesized by the catalytic decompositi ...  neutral before being dried overnight at 120 degC.
2859,10.1016/j.apcata.2007.06.018,something_else,Fe-Ru catalysts for Fischer-Tropsch synthesis were ... ion and produces a catalyst which does not sinter.
2860,10.1016/j.apcata.2007.06.018,something_else,Fe-Ru bimetallic catalysts for Fischer-Tropsch (FT ... upport interaction characteristic of CNT supports.
2861,10.1002/chem.201303623,something_else,A Schlenk tube charged with Togni reagent II (0.2  ...  chromatography (using I2 as a visualizing agent).
2862,10.1002/chem.201303623,something_else,When TEMPO (1.0 equiv) was added into the standard ... ectroscopy (see Supporting Information; Scheme 6).
2863,10.1002/chem.201303623,something_else,[a] Reaction conditions: [Cu(CH3CN)4]PF6 (0.15 equ ... 0 equiv) was added after 2 h. [b] Isolated yields.
2864,10.1016/j.solmat.2006.07.002,something_else,Optically smooth highly specularly reflecting alum ... ve abilities onto a contaminated aluminum surface.
2865,10.1002/chem.201303623,something_else,"To our delight, on enlarging the reaction scale to ...  obtained, affording 2 b in 90 % yield (Scheme 2)."
2866,10.1002/chem.201303623,something_else,"With the optimized reaction conditions in hand, we ...  standard conditions (Table 2, entries 22 and 23)."
2867,10.1002/chem.201303623,something_else,"[a] Reaction conditions: Cu cat. (0.15 equiv), lig ...  degC, argon atmosphere, 12 h. [h] NR=no reaction."
2868,10.1016/j.jlumin.2016.05.010,something_else,Samples: We used crystals supplied by Scientific M ... rown Er:YSO 0.005% sample was used as a reference.
2869,10.1016/j.ces.2008.03.005,something_else,"The terminal velocity of the particles can be used ... ing the following equation (Tek and Wilkes, 1974):"
2870,10.1016/j.ces.2008.03.005,something_else,"This paper describes the results of experiments in ... 5, Tsouris et al., 2006 and Tsouris et al., 2007)."
2871,10.1016/j.solmat.2006.07.002,something_else,The experimentally made absorbers were produced in ...  received the final heat treatment up to 400 degC.
2872,10.1016/j.solmat.2006.07.002,something_else,A spin coater KW-4A made by Chemat Technology was  ... ased through evaporation of the solution solvents.
2873,10.1002/chem.201303623,something_else,[a] Reaction conditions: [Cu(CH3CN)4]PF6 (0.15 equ ... ted 1 was isolated by flash column chromatography.
2874,10.1007/s10853-006-0438-4,something_else,Three Mo bicrystals were grown from the misoriente ... ture of about 1800 degC the beam was switched off.
2875,10.1016/j.tetlet.2013.11.100,something_else,"(a) Optimisation of the reaction conditions for th ... sel, 5 mg silica gel, No solvent, 70 degC, 10 min."
2876,10.1016/j.tetlet.2013.11.100,something_else,"Reaction conditions: the alcohol (0.5 mmol), diami ... d under microwave conditions as highlighted above."
2877,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out with aniline (1.0 mmo ... atalyst) in toluene (0.1 mL) at 110 degC for 17 h.
2878,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out using aniline (1.0 mm ... 0 mol %) in toluene (0.5 mL) at 110 degC for 40 h.
2879,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out with aniline (1.0 mmo ... atalyst) in toluene (0.1 mL) at 110 degC for 17 h.
2880,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out with aniline (1.0 mmo ... 0 mol %) in toluene (0.1 mL) at 110 degC for 17 h.
2881,10.1016/j.tet.2007.11.083,something_else,"Initially, we studied the reaction of aniline with ...  base; however, the yield was moderate (entry 10)."
2882,10.1016/j.jpowsour.2010.12.044,something_else,Aqueous inks with electrocatalyst concentration of ... proving the ink homogeneity over the GC electrode.
2883,10.1016/j.jpowsour.2010.12.044,something_else,"High performance (HP) 20% 1:1 Pt-Ru alloy on Vulca ... 9%), while CO gas was Linde 3.0 (purity >= 99.9%)."
2884,10.1016/j.ces.2008.10.017,something_else,Heterogeneous nucleation of clathrates from superc ... water mixtures and the effect of an added catalyst
2885,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out with primary amine (1 ... atalyst) in toluene (0.1 mL) at 110 degC for 17 h.
2886,10.1016/j.ces.2008.10.017,something_else,"For both systems (methane+water and xenon+water),  ... ooling rates were investigated: 0.5 and 1.5 K/min."
2887,10.1016/j.ces.2008.10.017,something_else,"The isothermal experiments were all performed with ... periments, new samples were prepared for each run."
2888,10.1016/j.ces.2008.10.017,something_else,The main focus of this work was hydrate nucleation ...  both the hydrate and ice nucleation temperatures.
2889,10.1007/s11661-014-2702-6,something_else,"Optical microscopy (OM), TEM, and APT were employe ... e-side Cs-corrected JEOL-2100F operated at 200 kV."
2890,10.1007/s11661-014-2702-6,something_else,"In the case of melt spinning, two Na-containing al ... lso performed for the controlled sand cast alloys."
2891,10.1007/s11661-014-2702-6,something_else,"In the case of controlled sand casting, experiment ... where the samples were prepared using arc melting."
2892,10.1007/s11661-014-2702-6,something_else,"Al-5 wt pct Si alloys (wt pct, used throughout thi ... refore, 0.44 ppm was used as an average P content."
2893,10.1016/j.watres.2011.09.015,something_else,Landfill leachate was collected from the Cabo Rojo ... s in the figures represent one standard deviation.
2894,10.1016/j.mssp.2008.01.002,something_else,"Subsequently, all the samples were chemically poli ... oscope (SIRM) after mechanical polish on one side."
2895,10.1016/j.ces.2008.10.017,something_else,Water-in-oil emulsions were prepared by first heat ... mograms and microscope images are shown in Fig. 1.
2896,10.1016/j.tsf.2010.03.150,something_else,"After dipping, a 200-nm-thick layer of p-type AlN: ... , and I-V measurements (Keithley SCS-4200 System)."
2897,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out using benzylamine (1. ... 0 mol %) in toluene (0.5 mL) at 110 degC for 40 h.
2898,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out with secondary amine  ... atalyst) in toluene (0.1 mL) at 110 degC for 17 h.
2899,10.1016/j.apcata.2007.06.019,something_else,Active carbon supported Ru catalysts were prepared ... experiment was decided based on the proton amount.
2900,10.1016/j.fuel.2007.06.002,something_else,"For all experiments a model biogas, consisting of  ... ce it will be removed at the pilot plant in Strem."
2901,10.1016/j.fuel.2007.06.002,something_else,The major reactor dimensions and operating paramet ... orage tank mass difference during the experiments.
2902,10.1016/j.jpowsour.2016.02.066,something_else,The electrochemical behavior was evaluated in two- ... n AC voltage signal of 5 mV from 100 kHz to 2 mHz.
2903,10.1016/j.tet.2007.11.083,something_else,"The reaction of benzylamine with chiral secondary  ...  oxidation of alcohols, which causes racemization."
2904,10.1016/j.tet.2007.11.083,something_else,(a) The reaction of pyrrolidine (1.0 mmol) with 1- ...  (1.0 mmol) at 110 degC gave 72% of tributylamine.
2905,10.1016/j.tet.2007.11.083,something_else,We also conducted a competitive reaction using ben ... -alkylation of primary amines to secondary amines.
2906,10.1016/j.tet.2007.11.083,something_else,In a septum-capped glass tube under an atmosphere  ... d 5-7) or column chromatography (entries 2 and 4).
2907,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out with secondary amine  ... atalyst) in toluene (0.1 mL) at 110 degC for 17 h.
2908,10.1016/j.tet.2007.11.083,something_else,In a heavy-walled glass reactor under an atmospher ... aphy (eluent: hexane/ethyl acetate/triethylamine).
2909,10.1016/j.tet.2007.11.083,something_else,In a heavy-walled glass reactor under an atmospher ... aphy (eluent: hexane/ethyl acetate/triethylamine).
2910,10.1016/j.tet.2007.11.083,something_else,In a heavy-walled glass reactor under an atmospher ... aphy (eluent: hexane/ethyl acetate/triethylamine).
2911,10.1016/j.tet.2007.11.083,something_else,In a heavy-walled glass reactor under an atmospher ... aphy (eluent: hexane/ethyl acetate/triethylamine).
2912,10.1016/j.tet.2007.11.083,something_else,In a heavy-walled glass reactor under an atmospher ... C analysis using undecane as an internal standard.
2913,10.1016/j.tet.2007.11.083,something_else,All reactions and manipulations were carried out u ...  commercially available and were used as received.
2914,10.1016/j.tet.2007.11.083,something_else,The reaction was carried out with benzylamine (1.0 ...  mmol) was added and stirred at 110 degC for 24 h.
2915,10.1016/j.tet.2007.11.083,something_else,"First, the reaction of benzylamine with 4-methoxyb ... ethodology. The results are summarized in Table 7."
2916,10.1016/j.tet.2007.11.083,something_else,To obtain an information concerning the reaction m ... t obviously supports our proposal described above.
2917,10.1016/j.tet.2007.11.083,something_else,In a heavy-walled glass reactor under an atmospher ... aphy (eluent: hexane/ethyl acetate/triethylamine).
2918,10.1002/app.25822,something_else,"Analytical grade diethylene glycol (DEG), N,N-dime ... ased from Aldrich Chemical Company, Milwaukee, WI."
2919,10.1016/j.tsf.2010.03.150,something_else,"Hybrid-structure p-type AlN:ZnO thin film-coated Z ... ), which was heated in an oven at 95 degC for 8 h."
2920,10.1016/j.apcatb.2014.08.025,something_else,"After photocatalytic reaction for 10 min, a sample ... on time = 9.5 min) were observed as intermediates."
2921,10.1002/app.42718,something_else,where t0 is the original thickness of sample (1 cm ... verage was considered as the characteristic value.
2922,10.1002/app.42718,something_else,"A series of amidated copolymers (EPDM-g-CCA-2-Am,  ... ation process of high-performance recyclable EPDM."
2923,10.1002/app.42718,something_else,where the Winsoluble is the dry weight of insolubl ... PDM-g-CCA extracted in acetone at 40degC for 48 h.
2924,10.1002/app.42718,something_else,where the dry weights of EPDM-g-CCA extracted in a ... t (wt %) was determined by the following equation:
2925,10.1002/app.42718,something_else,Citraconated EPDM (EPDM-g-CCA) was prepared by mel ... DM-g-CCA was determined by the following equation:
2926,10.1002/app.42718,something_else,"The EPDM (contents of ethylene, propylene, and eth ...  with different chain length are shown in Table 1."
2927,10.1016/j.jnucmat.2006.02.084,something_else,Thermal diffusivity measurements were carried out  ... ctor and plotted online with the help of software.
2928,10.1016/j.matchemphys.2016.05.033,something_else,"Highly coercive melt-spun Sm(Co, Fe, Cu, Zr)z magnets prepared by simple processing"
2929,10.1016/j.energy.2013.12.060,something_else,"SW: water supplied to the MED, in order to be desa ... or to the heat exchanger used for cooling the ACH;"
2930,10.1016/j.matchemphys.2016.05.033,something_else,"The sample milled for 3 h when isothermally aged a ...  of Hk of -10 kOe, iHC of 16 kOe and Br of 9.2 kG."
2931,10.1002/maco.201206816,something_else,"For preparation of T8 sol-gel, the aging time of s ...  very important from the industrial point of view."
2932,10.1002/maco.201206816,something_else,"Due to the use of sol-gels in industries, required ... 1) on the performance of coating was investigated."
2933,10.1002/maco.201206816,something_else,Hybrid nanostructured films were deposited on the  ... ture for 24 h and then heated at 120 degC for 1 h.
2934,10.1002/maco.201206816,something_else,"To prepare sol(2), acetylacetone and titanium(IV)  ... factors for all sol-gels and are given in Table 2."
2935,10.1002/maco.201206816,something_else,"Sol(1): nanoparticle free sol-gel films prepared b ... l-gel, sol(2), was prepared and mixed with sol(1)."
2936,10.1002/maco.201206816,something_else,TMSNAP sol-gel was prepared by controlled hydrolys ...  and metalorganic (nanoparticle) parts separately.
2937,10.1002/maco.201206816,something_else,The AA2024 alloy panel was cut to 1 cm x 1 cm and  ... ic cleaning successively in 2-propanol for 10 min.
2938,10.1016/j.tetlet.2013.11.100,something_else,The superior results obtained under closed vessel  ... tributing to the successful quinoxaline synthesis.
2939,10.1016/j.matchemphys.2016.05.033,something_else,The sintered samples were subjected to aging at 80 ...  but lower coercivity than sample A aged for 15 h.
2940,10.1016/j.apcatb.2014.08.025,something_else,To evaluate the role of the primary reactive speci ...  dissolved oxygen may play a role in the reaction.
2941,10.1016/j.energy.2013.12.060,something_else,DW (Desalinized Water): fresh water produced by the MED and supplied to final users.
2942,10.1111/ijac.12258,something_else,"Fly ash (Thermal power plant, Hefei, China), clay  ...  used in each composition are detailed in Table 3."
2943,10.1016/j.apcatb.2014.08.025,something_else,"The photocatalytic degradation experiments were ca ...  organic carbon analyzer (TOC-V, Shimadzu, Japan)."
2944,10.1016/j.apcatb.2014.08.025,something_else,The OPP (purity: 99.9%) was purchased from JK Chem ... tical grade and used without further purification.
2945,10.1016/j.apcatb.2014.08.025,something_else,Novel flower-like heterostructured β-Bi2O3/Bi2O2CO ... ble for the nearly complete mineralization of OPP.
2946,10.1016/j.matlet.2014.12.038,something_else,The tungsten boat was replaced by a three-wire tun ... inal thickness of the bimetallic layer was ~25 nm.
2947,10.1016/j.matlet.2014.12.038,something_else,Current was passed through the boat in increments  ... e gold in the tungsten boat was left unevaporated.
2948,10.1016/j.matlet.2014.12.038,something_else,In order to implement the VMD technique in this CT ... amber was pumped to a base pressure of ~ 4 mTorr .
2949,10.1016/j.matlet.2014.12.038,something_else,The platform was then attached to a system compris ... at the receptacle are also present in the chamber.
2950,10.1016/0921-5093(95)03342-4,something_else,Owing to the poor oxidation resistance of titanium ... dation resistance for CP Ti and the TiAlNb alloys.
2951,10.1016/j.energy.2013.12.060,something_else,"A plate-fin heat exchanger in the HW loop (HE2), t ... to be supplied to the fan-coils during the winter;"
2952,10.1016/j.jmbbm.2010.02.001,something_else,Density of Parafilm (0.77+-0.01 g/cm3) was given b ...  a caliper on a regular shaped sample of material.
2953,10.1016/j.jmbbm.2010.02.001,something_else,"For the characterization, 10.5 mm diameter x 12 mm ...  layer in between the two layers of bulk material."
2954,10.1016/j.jcis.2009.04.062,something_else,Electrochemical measurements were carried out with ... tum Design Physical Properties Measurement System.
2955,10.1016/j.jcis.2009.04.062,something_else,"Powder X-ray diffraction (PXRD) studies were carri ... upported on a copper grid, and then drying in air."
2956,10.1016/j.jcis.2009.04.062,something_else,The same procedure (discussed above for the synthe ... ed for the synthesis of Co-Ni alloy nanoparticles.
2957,10.1016/j.jcis.2009.04.062,something_else,"For the synthesis of Co and bimetallic Co-Ni nanop ... aligens, 99.5%), and isooctane (spectrochem, 99%)."
2958,10.1016/j.jeurceramsoc.2010.11.003,something_else,The bending strength was determined using prismati ... crosshead speed of 0.5 mm/min and a span of 16 mm.
2959,10.1016/j.jeurceramsoc.2010.11.003,something_else,"For mechanical characterization the tensile surfac ... r/polisher with a VECTOR power head, Buehler, UK)."
2960,10.1016/j.jssc.2014.03.019,something_else,Gibbsite powder (Al2(OH)6) with a density of ~2.4  ...  surface area of the original sample was 0.5 m2/g.
2961,10.1016/j.jmbbm.2010.02.001,something_else,Some 10.5 mm cylindrical samples (not used for com ... ity with water and observing the change in weight.
2962,10.1002/app.25822,something_else,"Realizing their importance, in the present study,  ... ir chemical interaction with drug and their sizes."
2963,10.1002/app.25822,something_else,"Novel polyurethanes (PUs) grafted with methoxypoly ... 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007"
2964,10.1016/j.fuel.2012.03.023,something_else,"The viscosities at 38 degC, determined as describe ... age VBN and U data, in the following general form:"
2965,10.1016/j.tet.2007.11.081,something_else,"To a solution of 25 (8.2-53 mg, 0.03-0.20 mmol) in ... ne/AcOEt=1:1) to afford 27a-h as shown in Table 5."
2966,10.1016/j.tet.2007.11.081,something_else,According to the procedure given for the preparati ... kyl iodide (4.5 mmol) gave 25 as shown in Table 5.
2967,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... calcd for C14H21NO3 (M+) 251.1520, found 251.1546."
2968,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... calcd for C13H17NO3 (M+) 235.1207, found 235.1202."
2969,10.1016/j.tet.2007.11.081,something_else,"To a solution of 21 (0.75 g, 6.5 mmol) in MeOH (30 ... calcd for C12H15NO3 (M+) 221.1051, found 221.1066."
2970,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ...  40 mmol) gave 22 (1.7 g, 65%) as a colorless oil."
2971,10.1016/j.tet.2007.11.081,something_else,"To a solution of 199 (2.7 g, 23 mmol) in CH2Cl2 (1 ... 1:1) to afford 21 (2.0 g, 73%) as a colorless oil."
2972,10.1016/j.tet.2007.11.081,something_else,"To a solution of 14 (50 mg, 0.13 mmol) in CH2Cl2 ( ... rified by MCC to afford 15c,h as shown in Table 4."
2973,10.1016/j.tet.2007.11.081,something_else,According to the procedure given for the preparati ... kyl iodide (2.8 mmol) gave 26 as shown in Table 5.
2974,10.1016/j.tet.2007.11.081,something_else,"To a solution of 14 (50 mg, 0.13 mmol) in CH2Cl2 ( ... xane/AcOEt=20:1) to afford 15 as shown in Table 4."
2975,10.1016/j.tet.2007.11.081,something_else,"To a solution of 127 (830 mg, 3.84 mmol) and 136 ( ... alcd for C18H19NO6S (M+) 377.0932, found 377.0943."
2976,10.1016/j.tet.2007.11.081,something_else,According to the procedure given for the preparati ... kyl iodide (2.8 mmol) gave 11 as shown in Table 3.
2977,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ...  calcd for C14H21NO (M+) 219.1622, found 219.1629."
2978,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... alcd for C19H23NO4S (M+) 361.1346, found 361.1353."
2979,10.1016/j.tet.2007.11.081,something_else,"To a solution of 3 (50 mg, 0.14 mmol) in CH2Cl2 (4 ... 0:1) to afford pyrrolidines 6 as shown in Table 2."
2980,10.1016/j.tet.2007.11.081,something_else,"To a solution of 3 (50 mg, 0.14 mmol) in CH2Cl2 (4 ...  calcd for C13H19NO (M+) 205.1466, found 205.1444."
2981,10.1016/j.tet.2007.11.081,something_else,"To a solution of BnONH2*HCl (16 g, 100 mmol) in H2 ... alcd for C18H21NO4S (M+) 347.1190, found 347.1191."
2982,10.1016/j.tet.2007.11.081,something_else,Melting points are uncorrected. 1H and 13C NMR spe ...  on precoated silica gel plates (E. Merck 60F254).
2983,10.1016/j.tet.2007.11.081,something_else,"To a solution of 14 (50 mg, 0.13 mmol) in CH2Cl2 ( ... alcd for C20H25NO6S (M+) 407.1401, found 407.1416."
2984,10.1016/j.tet.2007.11.081,something_else,We first picked up oxime ether 3 carrying the tosy ... benzyloxyamine5 followed by tosylation (Scheme 2).
2985,10.1016/j.tet.2007.11.081,something_else,"To a solution of 26 (8.2-53 mg, 0.03-0.20 mmol) in ... exane/AcOEt=1:1) to afford 28 as shown in Table 5."
2986,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... calcd for C18H19NO3 (M+) 297.1364, found 297.1381."
2987,10.1111/ijac.12251,something_else,Surface morphologies of the scales formed on coate ... (d) 20 h; (e) 40 h; (f) 60 h; (g) 80 h; (h) 100 h.
2988,10.1111/ijac.12251,something_else,"Before the emissivity measurements were performed, ... s measured, and thus, the emissivity was obtained."
2989,10.1016/j.jnucmat.2006.02.086,something_else,"Single crystals, after plastic deformation and dam ... and ammonia plus hydrogen peroxide plus water [9]."
2990,10.1016/j.jeurceramsoc.2010.12.003,something_else,High solids loading ceramic colloidal dispersions  ... le media with via comb-polyelectrolyte dispersants
2991,10.1016/j.jeurceramsoc.2010.12.003,something_else,"As this process is photo-gelcasting, the suspensio ... rodynamic flow rather than colloidal flocculation."
2992,10.1016/j.jeurceramsoc.2010.12.003,something_else,Three-dimensional objects are made from many thin  ... and characterizing photopolymerizable suspensions.
2993,10.1016/j.jeurceramsoc.2010.12.003,something_else,Photopolymerizable ceramics find application in ph ... he well-known techniques of photopolymerization.14
2994,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... ) calcd for C9H15NO (M+) 153.1153, found 153.1151."
2995,10.1016/j.tet.2007.11.081,something_else,"To a solution of NaOH (99 mg, 2.5 mmol) in THF-H2O ... lcd for C17H18NO3 (M+H+) 284.1286, found 284.1281."
2996,10.1016/j.tet.2007.11.081,something_else,"To a solution of 39a (25 mg, 0.08 mmol) in AcOH (1 ... ) calcd for C9H15NO (M+) 153.1153, found 153.1147."
2997,10.1016/j.tet.2007.11.081,something_else,"According to the reported procedure,14c the treatm ...  calcd for C19H39NO (M+) 281.3081, found 281.3070."
2998,10.1016/j.tet.2007.11.081,something_else,"To a solution of 33 (25 mg, 0.09 mmol) in AcOH (1. ... :1) to afford 35 (6.7 mg, 67%) as a colorless oil."
2999,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ...  calcd for C25H43NO (M+) 373.3343, found 373.3341."
3000,10.1016/j.tet.2007.11.081,something_else,"To a solution of 1-bromotetradecane (2.0 mL, 6.85  ... ere identical with those reported in literature.18"
3001,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... .4 mmol) gave 28b (26 mg, 63%) as a colorless oil."
3002,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... 34 mmol) gave 28a (28 mg, 70%) as a colorless oil."
3003,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... .5 mmol) gave 27b (28 mg, 68%) as a colorless oil."
3004,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ... 35 mmol) gave 27a (28 mg, 72%) as a colorless oil."
3005,10.1016/j.tet.2007.11.081,something_else,"According to the procedure given for the preparati ...  polar isomer 39b (62 mg, 41%) as a colorless oil."
3006,10.1016/j.jcat.2008.06.014,something_else,"Details of the preparation of the Pd-Ga intermetal ... iation, λ = 1.540598 Å , curved Ge monochromator)."
3007,10.1016/j.corsci.2013.07.004,something_else,The oxidation experiments were conducted at 1050 d ... e scanning rate was 2deg/min from 20deg to 110deg.
3008,10.1016/j.jelechem.2008.08.005,something_else,"Decay of 2,4-D with electrolysis time during the t ... power: (*) 20, (#) 60 and (Δ) 80 W; () EF process."
3009,10.1016/j.epsl.2012.01.002,something_else,Double-capsules were used for our experiments. We  ... xperiments were quenched by turning off the power.
3010,10.1016/j.epsl.2012.01.002,something_else,The starting material resembles terrigenous sedime ... ed to this starting material using a microsyringe.
3011,10.1016/j.jmatprotec.2005.08.008,something_else,The developed tests were developed on properly pre ... rly deformed and placed into the clamping systems.
3012,10.1016/j.ssc.2009.05.026,something_else,BaFe2As2 was prepared from a stoichiometric mixtur ... y diffraction using a Stoe Stadi P diffractometer.
3013,10.1016/j.solmat.2006.07.003,something_else,Topography of CPD on WO3 film selectively colored using 1 M HCl dissolved triple distilled water.
3014,10.1016/j.solmat.2006.07.003,something_else,"For the Kelvin probe, the intercalation is done on ... s show better electrochromic charge intercalation."
3015,10.1016/j.solmat.2006.07.003,something_else,Cyclic voltammogram of WO3 thin film on ITO coated ...  a reference electrode. The scan rate was 50 mV/s.
3016,10.1016/j.solmat.2006.07.003,something_else,The schematic of the solid state protonic electroc ... ch low sputtering rates are rather unconventional.
3017,10.1016/j.epsl.2012.01.002,something_else,"Electron microprobe (EMPA) analysis of mounted and ... ue, explaining the large analytical uncertainties."
3018,10.1016/j.jssc.2014.03.013,something_else,Polycrystalline Na2IrO3 was prepared via a method  ... but with an additional 2 week heating at 900 degC.
3019,10.1016/j.powtec.2008.01.023,something_else,Three-dimensional numerical simulations of a horiz ... s equivalent to a centrifugal acceleration of 7 g.
3020,10.1016/j.applthermaleng.2014.08.058,something_else,"The vacuum loop consists of a water pump, a tube a ... ler was installed to avoid the loss of the vapour."
3021,10.1016/j.applthermaleng.2014.08.058,something_else,The cooling water loop consists of a water tank wi ...  change the temperature of the micro-tube surface.
3022,10.1016/j.matchemphys.2016.05.035,something_else,Photocatalytic TiO2/adsorbent nanocomposites prepa ... al impregnation for wastewater treatment: a review
3023,10.1016/j.matchemphys.2016.05.035,something_else,Chromatographic analysis was performed using an ul ... te 30 units and capillary temperature of 355 degC.
3024,10.1016/j.matchemphys.2016.05.035,something_else,The photocatalytic performance of all composites w ... iation on horizontal surface is 1307 kW h m-2[17].
3025,10.1016/j.matchemphys.2016.05.035,something_else,A modified Hummer's method [16] was used for the p ...  investigated and compared with that of TA sample.
3026,10.1016/j.matchemphys.2016.05.035,something_else,"TiO2-P25 was supplied from Degussa (Germany). Trit ... was produced by a Milli-Q system (Millipore, USA)."
3027,10.1016/j.powtec.2008.01.023,something_else,The second set of numerical simulations was perfor ... t with the experimental result of Qian et al. [7].
3028,10.1016/j.corsci.2013.07.004,something_else,The chemical compositions of six ODS alloys referr ... ured using a balance with a resolution of 0.01 mg.
3029,10.1016/j.tsf.2015.01.039,something_else,Samples were deposited on Corning microscopy cover ... r during 1 h at each step of cumulative annealing.
3030,10.1016/j.ijhydene.2010.11.027,something_else,To demonstrate the effect of buffer particles amou ... ith mass ratio Al2O3/SnO2 > 0.8 in experiments IV.
3031,10.1016/j.jelechem.2008.08.005,something_else,"Solution pH was measured with an Eutech Instrument ... and 22.2 min for 2,4-D, DNOC and AB, respectively."
3032,10.1016/j.jelechem.2008.08.005,something_else,Aqueous solutions of 250 ml were prepared for each ...  according to previous studies on EF process [11].
3033,10.1016/j.jelechem.2008.08.005,something_else,Constant current bulk electrolyses were performed  ... ectrolysis to reach a stationary O2 concentration.
3034,10.1016/j.jelechem.2008.08.005,something_else,"Acetic acid, sulfuric acid, anhydrous sodium sulfa ... e was HPLC grade from VWR International (Prolabo)."
3035,10.1016/j.jelechem.2008.08.005,something_else,"The herbicides 2,4-D and DNOC as well as the azo d ... 9% provided by Sigma-Aldrich and used as received."
3036,10.1016/j.apgeochem.2013.07.023,something_else,When newly formed BMOs were repeatedly treated in  ...  activity in newly formed BMOs is at least 8 days.
3037,10.1016/j.apgeochem.2013.07.023,something_else,To evaluate the effect of coexisting Co(II) on Mn( ... an indicator for the growth of A. strictum KR21-2.
3038,10.1016/j.apgeochem.2013.07.023,something_else,To demonstrate the significance of the preformed B ... ut preformed BMO phase (incubated without Mn(II)).
3039,10.1016/j.enconman.2011.08.025,something_else,Coin cells of 2016 configuration have been assembl ... unched out and used as a cathode in the coin cell.
3040,10.1016/j.apgeochem.2013.07.023,something_else,The Mn(II) oxidase activity in the concentrated cr ... n(II) oxidizing rate throughout the reaction time.
3041,10.1016/j.apgeochem.2013.07.023,something_else,Two-step extraction using aqueous CuSO4 and hydrox ... ep extraction sequence is referred to as solid Mn.
3042,10.1016/j.apgeochem.2013.07.023,something_else,Newly formed BMOs were mixed with 0-1000 μM CoCl2  ...  and the structural changes in the resultant BMOs.
3043,10.1016/j.apgeochem.2013.07.023,something_else,"A. strictum KR21-2, which is capable of oxidizing  ... equestration experiments within 1 h after washing."
3044,10.1016/j.msea.2007.10.068,something_else,Electrolytic iron and high-purity copper were vacu ...  estimated to be ~50 μm from a previous study [2].
3045,10.1016/j.jelechem.2014.11.037,something_else,Cost of 2 mm SS 302 sheets on bulk purchase (clean ...  market is INR 120 [40] = 0.795 kg x 120 = INR 96.
3046,10.1016/j.jelechem.2014.11.037,something_else,Settling is one of the widely used low cost operat ... inuous thickener based on batch experimental data.
3047,10.1016/j.jelechem.2014.11.037,something_else,The complete setup of experiment is shown in Fig.  ... lectro chemical reactor (ECR) is given in Table 2.
3048,10.1016/j.jelechem.2014.11.037,something_else,Sugar industries are one of the largest agro based ... d in electrochemical treatment (ECT) of real SIWW.
3049,10.1016/j.apgeochem.2013.07.023,something_else,Mn(II) oxidase was recovered by dissolving the oxi ...  at -80 degC until the enzyme assay was performed.
3050,10.1016/j.apcata.2007.06.019,something_else,Reaction temperature dependence of the glycerol hy ...  = ethylene glycol + ethanol + methanol + methane.
3051,10.1016/j.jcat.2008.06.014,something_else,"To increase the active catalyst surface, chemical  ... ted to 10 mbar and stored under Ar in a glove box."
3052,10.1016/j.jcat.2008.06.014,something_else,"The active Pd surface area was determined by stepw ... ils are given elsewhere [29], [30], [31] and [32]."
3053,10.1016/j.actbio.2013.03.016,something_else,"For detection of platelet-leukocyte binding, 45 μl ... centrifuged at 200g for 5 min and washed with PBS."
3054,10.1016/j.actbio.2013.03.016,something_else,Tubings were closed by a silicone tubing and rotat ... d stored at 20-70 degC for further ELISA analyses.
3055,10.1016/j.actbio.2013.03.016,something_else,"Polyvinyl chloride tubes (3/8"" x 3/32"") with Carme ... ferent formulations of AgNPs (1, 3 and 30 mg l-1)."
3056,10.1016/j.actbio.2013.03.016,something_else,Modified Chandler-loop model. To analyze potential ... in a water bath at 37 degC to simulate blood flow.
3057,10.1016/j.actbio.2013.03.016,something_else,Silver nanoparticles were prepared by a rapid inje ... performed at the laboratory temperature (20 degC).
3058,10.1016/j.actbio.2013.03.016,something_else,"Silver nitrate (99.9%, Safina), sodium polyacrylat ... pared using deionized water (18 MΩ cm, Millipore)."
3059,10.1016/j.apcatb.2009.03.018,something_else,Isothermal transient response curves of CO2 and CO ... 5OH/40%H2O/59.4%He; Wcat = 0.3 g; FT = 200 mL/min.
3060,10.1016/j.apcatb.2009.03.018,something_else,Fig. 7 compares the transient isothermal (T = 650  ...  case of the natural calcite material as received.
3061,10.1016/j.actbio.2013.03.016,something_else,For evaluation of granulocyte and monocyte activat ... centrifuged at 200g for 5 min and washed with PBS.
3062,10.1016/j.apcatb.2009.03.018,something_else,DRIFTS-CO2-TPD was performed following a 30 min ga ... nes and after using Gausian peak line shapes [47].
3063,10.1016/j.apcatb.2009.03.018,something_else,The amount of carbon dioxide adsorbed on CaO (afte ... r the quantitative estimation of adsorbed CO2[46].
3064,10.1016/j.apcatb.2009.03.018,something_else,The experimental apparatus used for catalytic meas ... ed in 20%O2/80%He gas mixture at 850 degC for 2 h.
3065,10.1016/j.apcatb.2009.03.018,something_else,CO2 temperature-programmed desorption experiments  ... ter was made based on a 1 vol% CO2/He gas mixture.
3066,10.1016/j.tsf.2014.12.014,something_else,"Several of these samples, taken from four differen ... ions (04, 24 and 48 h) depending on the objective."
3067,10.1016/j.tsf.2014.12.014,something_else,"2.5 μm thick TiN coatings were deposited on to fla ...  2 x 350 W (Ptarget = 17.8 W/cm2), UBias = - 50 V."
3068,10.1016/j.tsf.2014.12.014,something_else,Different numbers of small hillocks (a) and high h ... e static attraction/adhesion of dust (V05 to V11).
3069,10.1016/j.matdes.2015.07.019,something_else,"Quality charts generated using Eqs. (1) ; (2), sho ...  followed by quenching in warm water and no aging."
3070,10.1016/j.matdes.2015.07.019,something_else,"Quality chart generated using Eqs. (1) ; (2), show ...  followed by quenching in warm water and no aging."
3071,10.1016/j.apcatb.2009.03.018,something_else,In situ DRIFTS-CO2 chemisorption studies were cond ... m-1 spectra resolution in the 4000-400 cm-1 range.
3072,10.1016/j.matdes.2015.07.019,something_else,The degassed molten alloys were poured in an ASTM  ... aulic MTS Mechanical Testing Machine (series 318).
3073,10.1016/j.actbio.2013.03.016,something_else,The release of platelet α-granules is only induced ... iple comparison test; C); *p < 0.05; ***p < 0.001.
3074,10.1016/j.jnucmat.2006.02.085,something_else,To optimize heat flow to and from the samples whil ... 0 degC/min were used for both heating and cooling.
3075,10.1016/j.fuel.2012.03.023,something_else,Once the viscosity blending number of a crude oil  ...  can be determined by using the invert of Eq. (8):
3076,10.1016/j.fuel.2012.03.023,something_else,The TBP distillation of all 117 investigated crude ... he AUTODEST 860 Fisher column from 1 to 0.2 mm Hg.
3077,10.1016/j.fuel.2012.03.023,something_else,> Model for crudes TBP express estimation from cru ... ht crudes TBP cut boiling up to 340 degC is 3.74%.
3078,10.1016/j.jpowsour.2010.12.045,something_else,The electrochemical measurements were made with 20 ... XRD using in situ coin cells with a Kapton window.
3079,10.1016/j.jelechem.2014.11.036,something_else,A novel [HPMIM] [Cl] ionic liquid was synthesized  ... d 92%. The reaction can be represented as follows:
3080,10.1016/j.jelechem.2014.11.036,something_else,"The overall chemical reactions for the preparation ... ale blue to a much deeper blue color, is observed."
3081,10.1016/j.solmat.2010.12.054,something_else,The NC films are deposited on ITO-coated glass sub ... e film thickness can be tuned from 100 nm to 1 μm.
3082,10.1016/j.solmat.2010.12.054,something_else,"In a first 50 mL flask, 0.05 g of CuCl (0.5 mmol o ... ersion is centrifuged again at 7000 rpm for 5 min."
3083,10.1016/0040-6031(92)85279-5,something_else,"The adducts MI3-tmtu (M = Sb, Bi; tmtu = tetrameth ... dity order AsI3 &>; SbI3 &>; BiI3 was established."
3084,10.1016/j.jelechem.2006.05.016,something_else,"In one experiment, the filtrate was evaporated und ... se of the benzene resonances of 4F and residual 3."
3085,10.1016/j.jelechem.2006.05.016,something_else,Cartoon depicting the purification of an electroch ... fluorous product from the excess fluorous reagent.
3086,10.1016/j.jelechem.2006.05.016,something_else,Electrochemically driven fluorous-phase separation ... und carbonyl group by a fluorous phosphine ligand.
3087,10.1016/j.jelechem.2006.05.016,something_else,Electrochemical measurements were performed in a n ... ocenium couple and have a precision of about 5 mV.
3088,10.1016/j.jelechem.2006.05.016,something_else,The crude salt was purified by flash chromatograph ... with a (*) overlap with a total integration of 9H.
3089,10.1016/j.jelechem.2006.05.016,something_else,"Sodium tetrakis(bis-3,5-trifluoromethylphenyl)bora ... lding 6.3 g (75%) of the crude [10.2-mim][BArF24]."
3090,10.1016/j.jelechem.2006.05.016,something_else,The synthesis of [10.2-mim]I was modified slightly ... 1 h precipitating 4.25 g of the white iodide salt.
3091,10.1016/j.jelechem.2006.05.016,something_else,Benzotrifluoride (Aldrich) was dried by refluxing  ...  Dr. Berth-Jan Deelman of Utrecht University [18].
3092,10.1016/j.tsf.2015.01.034,something_else,The a-SiCx passivation layer was deposited on 2 x  ... process was introduced in our previous paper [18].
3093,10.1016/j.jcat.2008.06.014,something_else,"Carbon monoxide chemisorption measurements were ca ... , Westfalen Gas, Germany) were performed at 300 K."
3094,10.1016/j.matdes.2015.07.019,something_else,Both B356 and B357 alloys were used in this study. ... he alloys used in both parts of the present study.
3095,10.1016/j.jpcs.2014.04.016,something_else,"After reduction, the reaction chamber was cooled t ... ials were dried and stored in a vacuum desiccator."
3096,10.1016/j.fuproc.2015.01.013,something_else,The process of transesterification reaction was ca ... ration is presented in (schematic diagram) Fig. 2.
3097,10.1016/j.fuproc.2015.01.013,something_else,The dried seeds of Aamla (10 g) were crushed into  ... tracted oil was determined using expression 1[13].
3098,10.1016/j.fuproc.2015.01.013,something_else,The Aamla plant mature seeds were collected throug ... l grade and used as such without any purification.
3099,10.1016/j.fuproc.2015.01.013,something_else,"In the present research work, non-edible oil sourc ... d compared with ASTM D6751 and EN 14214 standards."
3100,10.1007/s10854-008-9767-1,something_else,An automated Shimadzu XRD-7000 diffractometer was  ... λ = 1.54056 Å) using a scanning speed of 2deg/min.
3101,10.1007/s10854-008-9767-1,something_else,The sintered billets were subsequently extruded at ... pared to samples extruded at room temperature [5].
3102,10.1016/j.jmmm.2009.05.023,something_else,The mean particle hydrodynamic diameter of the unc ... r obtained from DLS of the uncoated nanoparticles.
3103,10.1016/j.jmmm.2009.05.023,something_else,"A 1:2 dilution of nanoparticle solution in DMEM+FB ... aMax Gemini EM, Molecular Devices, Sunnyvale, CA)."
3104,10.1016/j.fuproc.2015.01.013,something_else,"At the end, the mixture was separated into two lay ... ferant biodiesel was calculated using Eq. (2)[14]."
3105,10.1016/j.jmmm.2009.05.023,something_else,Cells were counted and seeded onto 96 well plates  ... . The pH was adjusted to 7.0 by adding 0.5 M NaOH.
3106,10.1016/j.jmmm.2009.05.023,something_else,Dry CMDx-MZF particles were sterilized at 121 degC ... ran coating remains stable after being autoclaved.
3107,10.1016/j.jmmm.2009.05.023,something_else,Hydrodynamic diameter and zeta potential were meas ... s done with a Siemens B500 DACO-MP Diffractometer.
3108,10.1016/j.jmmm.2009.05.023,something_else,The attachment of carboxymethyl-dextran chains to  ...  were dried in a vacuum oven at 60 degC overnight.
3109,10.1016/j.jcat.2008.06.014,something_else,To improve the flow characteristics the correspond ... hmark catalyst for studies with gas composition B.
3110,10.1016/j.jcat.2008.06.014,something_else,Acetylene hydrogenation experiments were carried o ...  gases were obtained from Westfalen Gas (Germany).
3111,10.1016/j.jcat.2008.06.014,something_else,Catalytic investigations were performed in a plug  ... injection and separation took between 4 and 5 min.
3112,10.1016/j.jmmm.2009.05.023,something_else,CaCo-2 cells and MCF-7 cells were purchased from A ...  the flask was diluted to seed experimental wells.
3113,10.1016/j.matdes.2015.07.019,something_else,The present work was performed on B357 alloy conta ... ontaining low levels of Fe with high levels of Mg.
3114,10.1016/j.fuproc.2015.01.013,something_else,The synthesized biodiesel sample was characterized ... e of internal standard methyl heptadecanoate [15].
3115,10.1016/j.fuproc.2015.01.013,something_else,"Cloud Point test for the biodiesel samples was per ... irst cloud appeared in the test tube bottom"" [21]."
3116,10.1016/j.jpcs.2014.04.016,something_else,"Oxide powder (2.0 g), calcium chloride (100 g), an ... oxides can be expressed by the following reaction:"
3117,10.1016/j.jpcs.2014.04.016,something_else,Three types of commercially available titanium oxi ... r the reduction of titanium oxides in molten salt.
3118,10.1016/j.cattod.2012.08.021,something_else,"After reduction, the temperature was decreased to  ... he gas outlet or to modify the CO conversion rate."
3119,10.1016/j.cattod.2012.08.021,something_else,"During the in situ activation treatment, the catal ... was maintained at the 400 degC set-point for 10 h."
3120,10.1016/j.cattod.2012.08.021,something_else,The cobalt-based model catalyst was prepared by in ... alyst was calcined at 400 degC under dry air flow.
3121,10.1016/j.tsf.2005.04.120,something_else,Pt50Mn50/Ni80Fe20 exchange-biased bilayers were pr ... eld of about 150 Oe to induce magnetic anisotropy.
3122,10.1016/j.electacta.2007.02.027,something_else,"After the treatment in Cell II, the electrode was  ... erformed according to the standard procedures [3]."
3123,10.1016/j.electacta.2007.02.027,something_else,"After the polymer deposition, the electrode was th ... gn below, the treatment potential used was -0.5 V."
3124,10.1016/j.fuproc.2015.01.013,something_else,"Four blend samples B5, B10, B15 & B20 were prepare ... 000, Germany), which was accurate to 0.01 mg [18]."
3125,10.1016/j.electacta.2007.02.027,something_else,Polybithiophene was deposited galvanostatically in ... otential and current profiles are given in Fig. 1.
3126,10.1016/j.electacta.2007.02.027,something_else,"2,2-Bithiophene (Aldrich) was purified through vac ... solutions were made right before the measurements."
3127,10.1016/j.fuproc.2015.01.013,something_else,Water content is considered as a purity indicator  ...  problem in the fuel filter system of engine [42].
3128,10.1016/j.fuproc.2015.01.013,something_else,"Effects of solid base and magnetic oxide catalyst  ... degC), reaction time (2 h) and stirring (600 rpm)."
3129,10.1016/j.fuproc.2015.01.013,something_else,"0.25 g of sample (B100, B5, B10, B15, B20 & petro- ... labeled glass tube for AAS spectroscopic analysis."
3130,10.1016/j.fuproc.2015.01.013,something_else,"Flash Point is defined as ""the temperature at whic ... als with continuous interruption of stirring [21]."
3131,10.1016/j.fuproc.2015.01.013,something_else,The acid number of oil and biodiesel was determine ...  (FFA) number of oil was determined using Eq. (7).
3132,10.1016/j.fuproc.2015.01.013,something_else,Water content test of the samples was performed in ... d. Water content was calculated using Eq. (6)[21].
3133,10.1016/j.fuproc.2015.01.013,something_else,Pour Point test of the entire samples was performe ...  intervals of 3 degC for flow characteristic [21].
3134,10.1016/j.electacta.2007.02.027,something_else,For AFM and current-sensing AFM (CS-AFM) measureme ... t of residual solvent content on the conductivity.
3135,10.1016/j.ab.2004.07.025,something_else,"Polymerase chain reaction (PCR) amplification of T ... spectively (Table 1), as described previously [6]."
3136,10.1016/j.apcata.2007.06.019,something_else,Reaction temperature dependence of the glycerol hy ...  = ethylene glycol + ethanol + methanol + methane.
3137,10.1016/j.apcata.2007.06.019,something_else,Dependence on A70 amount of the glycerol hydrogeno ...  = ethylene glycol + ethanol + methanol + methane.
3138,10.1016/j.polymer.2008.04.044,something_else,"A 300 mL three-necked flask was equipped with a th ...  6.80; N, 4.50. Found: C, 88.52; H, 7.01; N, 4.51."
3139,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from 4-(trimethylsily ...  6.52; N, 3.35. Found: C, 83.15; H, 6.78; N, 3.20."
3140,10.1016/j.polymer.2008.04.044,something_else,"A 500 mL three-necked flask was equipped with a th ...  5.54; N, 4.05. Found: C, 90.39; H, 5.64; N, 4.02."
3141,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from 4-(trimethylsily ... 1.6, 130.6, 123.1, 122.4, 122.3, 90.7, 88.7, -1.3."
3142,10.1016/j.polymer.2008.04.044,something_else,"A 1 L three-necked flask was equipped with a three ... .5, 128.5, 128.3, 122.9, 122.4, 122.2, 90.5, 88.3."
3143,10.1016/j.polymer.2008.04.044,something_else,"TaCl5 (Strem) as catalyst was used as received, wh ... e prepared according to the literature procedures."
3144,10.1016/j.polymer.2008.04.044,something_else,The molecular weights of polymers were estimated b ... ein were calibrated using ferrocene as a standard.
3145,10.1016/j.actamat.2008.06.012,something_else,Cylindrically shaped samples 7 mm in diameter and  ... interface contained interfacial dislocations [11].
3146,10.1016/j.cemconres.2016.06.003,something_else,The experimental procedure involves the mixing of  ...  the remaining 350 l is used to fill the formwork.
3147,10.1016/j.jeurceramsoc.2015.01.032,something_else,In situ characterization of the shrinkage behavior ... pacts during sintering by using heating microscopy
3148,10.1016/j.jeurceramsoc.2015.01.032,something_else,In order to characterize pore and particle orienta ... ermined by calculating the area fraction of pores.
3149,10.1016/j.jeurceramsoc.2015.01.032,something_else,The dried green sheets with a thickness between 24 ...  from the measured bulk and theoretical densities.
3150,10.1016/j.jeurceramsoc.2015.01.032,something_else,Tape casting was carried out on a tape-casting mac ... d at room temperature without additional air flow.
3151,10.1016/j.jeurceramsoc.2015.01.032,something_else,Tape casting slurries with a solid content of 28 v ... this study and also the density of the components.
3152,10.1016/j.jeurceramsoc.2015.01.032,something_else,"Spherical alumina powders SP (Sumitomo Chemical Co ... 2000, Malvern Instruments, London, Great Britain)."
3153,10.1016/j.jmmm.2009.05.022,something_else,The La1-xSrxMnO3 (x=0.33) films studied here were  ... sistivity versus temperature occurred near ~345 K.
3154,10.1016/j.msea.2017.05.044,something_else,The commercially cold drawn polycrystalline copper ... he Focus Ion Beam in a Quanta 3D Dual Beam system.
3155,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from N-isopropylanili ...  7.17; N, 3.99. Found: C, 88.61; H, 7.25; N, 3.96."
3156,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from carbazole and 6  ...  6.06; N, 3.37. Found: C, 83.43; H, 6.09; N, 3.65."
3157,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from indole in a mann ...  5.15; N, 4.77. Found: C, 90.33; H, 5.26; N, 4.84."
3158,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from indole and 6 in  ...  6.34; N, 3.83. Found: C, 82.38; H, 6.49; N, 3.86."
3159,10.1016/j.cattod.2006.05.014,something_else,"Reaction conditions: cat. 50 mg; cyclopentene, 10  ... ant, 10 mmol; MeCN, 10 mL; temp., 313 K; time 2 h."
3160,10.1016/j.cattod.2006.05.014,something_else,"Reaction conditions: cat., 50 mg; cyclopentene, 10 ... , 48 for TS-1 and 34 for Ti-MWW-dry, respectively."
3161,10.1016/j.cattod.2006.05.014,something_else,The liquid-phase oxidation of alkenes with hydroge ... ied by the titration with 0.1 M Ce(SO4)2 solution.
3162,10.1016/j.cattod.2006.05.014,something_else,The liquid-phase adsorption was carried out in a g ... chromatography to determine the adsorption amount.
3163,10.1002/jcp.21264,something_else,MDCK cells were plated at a density of 1.2 x 104 c ... ed out using the LSM 5 image browser (Carl Zeiss).
3164,10.1002/jcp.21264,something_else,Cell lines were plated on glass coverslips (Bellco ...  cells with condensed chromatin were not included.
3165,10.1002/jcp.21264,something_else,The ability of MDCK cells to form branching tubule ... less than five times it's width and is unbranched.
3166,10.1016/j.tet.2007.11.089,something_else,"The above-described hydrogenated product (10 mg, 0 ...  M+H+) calcd for C37H66O8 639.483, found 639.4813."
3167,10.1002/jcp.21264,something_else,"Cells were seeded at 106 cells per 100 mm Petri di ... ng dye reagent concentrate (BIORAD, Hercules, CA)."
3168,10.1016/j.polymer.2008.04.044,something_else,"Membranes (thickness ca. 100 μm) of poly(1b), poly ... rd the rate of solvent evaporation (ca. 3-5 days)."
3169,10.1016/j.polymer.2008.04.044,something_else,Polymerizations were carried out in a Schlenk tube ... thanol and its yield was determined by gravimetry.
3170,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from 8 and 4-bromo-N, ...  4.14; N, 3.38. Found: C, 75.17; H, 4.27; N, 3.20."
3171,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from 3,4-dichloroiodo ... .8, 132.4, 131.0, 130.2, 123.1, 102.4, 96.7, -0.2."
3172,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from 3,4-difluoroiodo ...  4.49; N, 3.67. Found: C, 81.62; H, 4.77; N, 3.64."
3173,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from 3-methylindole a ...  6.64; N, 3.69. Found: C, 82.12; H, 6.92; N, 3.60."
3174,10.1016/j.polymer.2008.04.044,something_else,"The compound was synthesized from 3-methylindole i ...  5.57; N, 4.56. Found: C, 90.03; H, 5.69; N, 4.63."
3175,10.1002/jcp.21264,something_else,Anti-HA (mHA.11) was purchased from Covance (Berke ... re pretreated for 1 h at a concentration of 20 uM.
3176,10.1016/j.tet.2007.11.089,something_else,"A solution of NaOAc (100 mg, 1.2 mmol) in water (2 ...  (9H, s). MS (ESI): m/z: 981 [M+H]+, 1003 [M+Na]+."
3177,10.1016/j.tet.2007.11.089,something_else,"The homoallylic alcohol compound 12a (13 mg, 0.02  ... 1, -4.44. MS (ESI): m/z: 979 [M+H]+, 1001 [M+Na]+."
3178,10.1016/j.tet.2007.11.089,something_else,"Compound 17 (610 mg, 1.2 mmol) was dissolved in 10 ... , 28.98, 28.84, 25.82, 25.07, 18.92, 17.99, -4.50."
3179,10.1016/j.fuel.2012.03.024,something_else,High purity alum (>99.9%) has also been prepared f ... e conditions the crystalline α-Al2O3 was observed.
3180,10.1016/j.fuel.2012.03.024,something_else,"In a more recent study, a CFA reported to have an  ... ess, an extraction efficiency of 90% was reported."
3181,10.1016/j.fuel.2012.03.024,something_else,Shabtai and Mukmenev [71] described a novel biomag ... precipitate was obtained by raising the pH to 6.5.
3182,10.1016/j.fuel.2012.03.024,something_else,In contrast CFA pelletised with fine coal and lime ... . A 92-97% TiO2 by-product could also be produced.
3183,10.1007/s10854-014-2259-6,something_else,Undoped and Co-doped ZnO thin films with different ... duction in the UV and visible emissions intensity.
3184,10.1016/j.cej.2007.11.011,something_else,mechanically stirred tanks in which the driving fo ... gas dispersion is the power supplied by impellers;
3185,10.1016/j.chroma.2014.07.058,something_else,"The recoveries of method were evaluated by spiking ... the different teas, tea infusion and soil samples."
3186,10.1016/j.chroma.2014.07.058,something_else,"The SPE procedure was used to pre-concentrate, so  ... /v) because of its effectiveness for the analytes."
3187,10.1016/j.fuel.2012.03.024,something_else,Ceramic microfiltration tubular membranes were pro ... r size distribution than a single coated membrane.
3188,10.1016/j.chroma.2014.07.058,something_else,The elution recoveries of the four target enantiom ... luted by different compositions of hexane/acetone.
3189,10.1016/j.chroma.2014.07.058,something_else,"Cis-epoxiconazole and indoxacarb were fairly lipop ... n. Therefore, we applied the overnight extraction."
3190,10.1016/j.chroma.2014.07.058,something_else,"In addition, the retention and resolution of analy ... iling, leading to decreased detection sensitivity."
3191,10.1016/j.chroma.2014.07.058,something_else,"TFA + AMF-1 to TFA + AMF-3 means the 2.0 mmol/L AM ... ded TFA at 0.20%, 0.10%, and 0.020%, respectively."
3192,10.1016/j.chroma.2014.07.058,something_else,"AMF-1 to AMF-7 means the AMF aqueous solution from ... 10 mmol/L, 20 mmol/L, and 50 mmol/L, respectively;"
3193,10.1016/j.chroma.2014.07.058,something_else,"AMA-1 to AMA-7 means the AMA aqueous solution from ... 10 mmol/L, 20 mmol/L, and 50 mmol/L, respectively;"
3194,10.1016/j.chroma.2014.07.058,something_else,"The separation was performed on a Lux 3 μ Cellulos ... e at 40:60, 30:70, 20:80, and 10:90, respectively."
3195,10.1016/j.chroma.2014.07.058,something_else,Representative fresh tea leaf and soil samples--at ... calculate the coefficient of green tea processing.
3196,10.1016/j.chroma.2014.07.058,something_else,Each experimental treatment consisted of three rep ... oxacarb (30% WDG) was applied at 133.2 mg a.i./kg.
3197,10.1016/j.chroma.2014.07.058,something_else,"Because of the complexity of the tea extracts, the ... elected as the eluent solution for sample cleanup."
3198,10.1016/j.cattod.2006.05.014,something_else,"Reaction conditions: cat. 50 mg.; cyclopentene, 10 ... H2O2, 10 mmol; MeCN, 10 mL; temp. 313 K; time 2 h."
3199,10.1016/j.fuel.2012.03.024,something_else,Another promising method appears to be that of sol ...  as much as 97% in less than 3 min of mixing time.
3200,10.1016/j.fuel.2012.03.024,something_else,CFA has been investigated for its potential as a s ... ective a materials synthesised from pure reagents.
3201,10.1016/j.tet.2007.11.089,something_else,"A solution of N,N-diisopropylamine (424 μl, 3.0 mm ... , 25.96, 24.37, 21.29, 20.99, 17.98, 14.16, -3.85."
3202,10.1016/j.tet.2007.11.089,something_else,"A mixture of the above-described TBS-protected tos ... , 28.88, 25.83, 24.88, 18.05, 13.98, -4.36, -4.56."
3203,10.1016/j.tet.2007.11.089,something_else,"To the above-described tosylate product (2.7 g, 7. ... , 25.74, 25.70, 24.73, 21.62, 18.02, -4.56, -4.81."
3204,10.1016/j.tet.2007.11.089,something_else,"TsCl (2.37 g, 12 mmol) was added in portions to a  ... , 32.56, 29.27, 29.18, 28.88, 28.75, 25.09, 21.54."
3205,10.1016/j.tet.2007.11.089,something_else,"To a well-stirred solution of potassium carbonate  ... , 33.76, 33.18, 29.56, 29.36, 29.02, 28.87, 25.51."
3206,10.1016/j.tet.2007.11.089,something_else,"To a solution of (-)-B-allyldiisopinocampheylboran ... 43, -4.46. MS (ESI): m/z: 627 [M+H]+, 649 [M+Na]+."
3207,10.1016/j.tet.2007.11.089,something_else,"DMSO (340 ml, 4.4 mmol) in 2 ml dichloromethane wa ... , 18.15, 18.13, 14.10, -4.21, -4.27, -4.27, -4.42."
3208,10.1016/j.tet.2007.11.089,something_else,"The TBS-protected compound 9 (605 mg, 0.86 mmol) a ... 46, -4.48. MS (ESI): m/z: 691 [M+H]+, 713 [M+Na]+."
3209,10.1016/j.fuel.2012.03.024,something_else,There have been several approaches to the extracti ... recovery of 83% of the Ga in the initial solution.
3210,10.1016/j.tet.2007.11.089,something_else,"TBSOTf (230 μl, 1.0 mmol) was added to a solution  ... 99, -5.06. MS (ESI): m/z: 687 [M+H]+, 709 [M+Na]+."
3211,10.1016/j.tet.2007.11.089,something_else,"DMSO (0.4 ml, 5 mmol) in 2 ml dichloromethane was  ... , 81.67, 77.32, 66.70, 28.47, 28.38, 27.90, 27.29."
3212,10.1016/j.tet.2007.11.089,something_else,"TBHP (0.1 ml, 0.5-0.6 mmol, 5-6 M in decane) was a ... 41, 27.38. MS (ESI): m/z: 307 [M+H]+, 329 [M+Na]+."
3213,10.1016/j.tet.2007.11.089,something_else,"Benzoyl chloride (0.37 ml, 3.1 mmol) was added dro ...  114.58, 69.49, 69.04, 33.64, 33.09, 31.87, 28.45."
3214,10.1016/j.tet.2007.11.089,something_else,"Freshly cut pieces of Na metal (900 mg) were added ...  114.62, 71.80, 66.74, 33.68, 32.81, 31.89, 28.63."
3215,10.1016/j.tet.2007.11.089,something_else,"Compound 3 (20 g, 150 mmol) was added to the well- ... (1H, m), 2.56 (1H, m), 2.27 (4H, m), 1.60 (2H, m)."
3216,10.1016/j.tet.2007.11.089,something_else,All reactions were carried out under an inert argo ...  ionization time-of-flight reflectron experiments.
3217,10.1016/j.tet.2007.11.089,something_else,"Separately, alkene 13 was synthesized from butyrol ... eported data for the natural 27-hydroxybullatacin."
3218,10.1016/j.fuel.2012.03.024,something_else,Mesoporous silica SBA-16 has been manufactured usi ... ource than when using pure raw materials (4.1 nm).
3219,10.1016/j.tet.2007.11.089,something_else,"BuLi (2.5 M in hexanes, 1.1 ml, 2.75 mmol) was add ... 50, -5.03. MS (ESI): m/z: 573 [M+H]+, 595 [M+Na]+."
3220,10.1002/app.26086,something_else,The TPU used in this study is a commercial materia ... tIPDI were used as reactive modifiers for the TPU.
3221,10.1002/app.26086,something_else,"A Brabender (Hackensack, NJ) single-screw extruder ... 60 rpm and between 170 and 220degC, respectively)."
3222,10.1002/app.26086,something_else,Size exclusion chromatography measurements were pe ... sults as a more time-consuming mass measurement.32
3223,10.1016/j.tet.2008.06.080,something_else,Lithium diisopropylamide 1.8 M in THF/heptane/ethy ... for C38H56N2O423Na120Sn: 747.3159; found 747.3183.
3224,10.1016/j.tet.2008.06.080,something_else,"To a solution of bisvinylphosphate 3 (1.00 g, 1.28 ... alcd for C14H22N2O423Na: 305.1477; found 305.1482."
3225,10.1016/j.tet.2008.06.080,something_else,Compound 4h was prepared according to the general  ... cd for C22H26N2O423NaS2: 469.1231; found 469.1243.
3226,10.1016/j.tet.2008.06.080,something_else,"Compound 4g was prepared according to the general  ... ), 154.4 (s). MS (IS): m/z=515 [MH]+, 537 [M+Na]+."
3227,10.1016/j.tet.2008.06.080,something_else,"Compound 4f was prepared according to the general  ...  5.53; N, 5.12. Found: C, 65.95; H, 5.38; N, 5.04."
3228,10.1016/j.tet.2008.06.080,something_else,"To a solution of bisvinylphosphate 3 (0.300 g, 0.3 ... alcd for C26H30N2O423Na: 457.2103; found 457.2104."
3229,10.1016/j.tet.2008.06.080,something_else,Compound 4d was prepared according to the general  ... alcd for C32H36N4O623Na: 595.2532; found 595.2538.
3230,10.1016/j.tet.2008.06.080,something_else,"Compound 4c was prepared according to the general  ... ), 151.1 (s). MS (IS): m/z=483 [MH]+, 495 [M+Na]+."
3231,10.1016/j.tet.2008.06.080,something_else,Compound 6b was prepared according to the general  ... cd for C29H38N2O423NaSi: 529.2486; found 529.2511.
3232,10.1016/j.tet.2008.06.080,something_else,"Compound 4b was prepared according to the general  ...  7.84; N, 8.38. Found: C, 64.74; H, 7.79; N, 8.19."
3233,10.1016/j.tet.2008.06.080,something_else,All the solvents used for reactions were distilled ... ether (P.E.) had a 40-60 degC boiling point range.
3234,10.1016/j.tet.2008.06.080,something_else,"Conditions: (i) 1.2 equiv LDA, THF, -78 degC, 20 min; (ii) 5 equiv electrophile, -78 degC, 30 min."
3235,10.1016/j.tet.2008.06.080,something_else,"Conditions: (i) 2.5 equiv LDA, THF, -78 degC, 1 h; ... min; (iii) 5 equiv electrophile, -78 degC, 30 min."
3236,10.1016/j.tet.2008.06.080,something_else,"Conditions: (i) 10 mol % PdCl2(PPh3)2, THF, rt, 15 ... iv RB(OH)2, 3 equiv Na2CO3 2 M, EtOH, reflux, 2 h."
3237,10.1016/j.tet.2008.06.080,something_else,"In the course of our investigations on the synthes ...  1,4-pyrazines was investigated in a second stage."
3238,10.1016/j.cplett.2012.05.007,something_else,The feasibility of the CdSe QDs deposited on the T ... QDSSCs to maximize the photoconversion efficiency.
3239,10.1016/j.cplett.2012.05.007,something_else,A quartz cuvette was utilized to set up solar cell ...  to 200-300 degC to prepare the counter electrode.
3240,10.1016/j.cplett.2012.05.007,something_else,"CdSe QDs synthesized by hot injection method were  ... alized unattached QDs, air dried and kept in dark."
3241,10.1016/j.tet.2008.06.080,something_else,"To a stirred solution of bisvinylphosphate 3 (0.30 ... ), 149.7 (s). MS (IS): m/z=547 [MH]+, 569 [M+Na]+."
3242,10.1016/j.cplett.2012.05.007,something_else,Acetonitrile solution containing 0.14 M mercapto p ... ain dried to obtain functionalized TiO2 electrode.
3243,10.1016/j.tet.2008.06.080,something_else,Compound 6c was prepared according to the general  ... alcd for C36H42N2O823Na: 653.2838; found 653.2847.
3244,10.1016/j.tet.2008.06.080,something_else,"Compound 6e was prepared according to the general  ... ), 151.9 (s), 163.3 (s). MS (IS): m/z=515 [M+Na]+."
3245,10.1016/j.optmat.2016.05.058,something_else,60 mL of 5 M aqueous NaOH was added to 50 mL of TH ... t the end purified by several washings in ethanol.
3246,10.1016/j.optmat.2016.05.058,something_else,"A solution of AnCl2 (2.75 g, 10 mmol) and tripheny ... l times with diethyl ether and dried under vacuum."
3247,10.1016/j.optmat.2016.05.058,something_else,"A mixture of anthracene (1.83 g, 10 mmol), parafor ... before an ultimate precipitation in diethyl ether."
3248,10.1016/j.optmat.2016.05.058,something_else,"Dimethylforamide was and distilled over Calcium hy ... brated with ferrocene, before each reductive scan."
3249,10.1002/cbic.200500479,something_else,"We used a TE300 Nikon inverted microscope with a m ... ased from Chroma Technology Corp., Rockingham, VT."
3250,10.1002/cbic.200500479,something_else,For the studies to count cells adhered to EGF-SLBs ... using bright-field and epifluorescence microscopy.
3251,10.1002/cbic.200500479,something_else,"A human breast epithelial cell line, MCF-10a, was  ... ed to the EGF-SLB. All other steps were as before."
3252,10.1002/cbic.200500479,something_else,EGF-modified SLBs were fabricated with by the foll ... using bright-field and epifluorescence microscopy.
3253,10.1016/j.tet.2008.06.080,something_else,Compound 6d was prepared according to the general  ... alcd for C27H30N2O523Na: 485.2052; found 485.2049.
3254,10.1016/j.jnucmat.2013.04.018,something_else,Field emission scanning electron microscopy (SEM H ...  fracture hydrocarbon-coated Si crystal specimens.
3255,10.1016/j.solmat.2006.07.009,something_else,The chemicals used are triblock copolymer (Pluroni ... 45 μm PVDF filter before the spectral measurement.
3256,10.1016/j.tet.2008.06.080,something_else,Compound 8d was prepared according to the method d ... ]+ calcd for C22H18N4O2: 370.4102; found 370.4104.
3257,10.1016/j.tet.2008.06.080,something_else,Compound 8c was prepared according to the method d ... ]+ calcd for C20H12N2S2: 344.0441; found 344.0430.
3258,10.1016/j.tet.2008.06.080,something_else,Compound 8b was prepared according to the method d ... M]+ calcd for C12H8N2S2: 244.0128; found 244.0132.
3259,10.1016/j.tet.2008.06.080,something_else,"Method 2: to a solution of 4e (0.080 g, 1.80 mmol, ... y using the same work-up as described in method 1."
3260,10.1016/j.tet.2008.06.080,something_else,"Method 1: to a solution of N,N-bis-(tert-butoxycar ... ted to afford 8a as a beige solid (0.041 g, 100%)."
3261,10.1016/j.tet.2008.06.080,something_else,Lithium diisopropylamide 1.8 M in THF/heptane/ethy ... alcd for C16H24N2O623Na: 363.1532; found 363.1528.
3262,10.1016/j.solmat.2006.07.009,something_else,Nanoporous SBA-15 was prepared by using microwave  ...  very intensively with hot doubly distilled water.
3263,10.1016/j.chroma.2014.07.058,something_else,A total of forty different brands of real market t ... determination of cis-epoxiconazole and indoxacarb.
3264,10.1016/j.cplett.2012.05.007,something_else,ITO electrodes (Nippon glass) were first cleaned w ... and the same entire procedure was repeated thrice.
3265,10.1016/j.jphotochem.2014.11.021,something_else,The InVO4/TiO2 heterojunction system was prepared  ... s ranged from 0.25 to 3 wt.% with respect to TiO2.
3266,10.1016/j.bbagen.2005.12.016,something_else,"The normal Krebs solution contained: 144 mM NaCl,  ... ES (increased to 10 mM) and 0.2 mM EGTA was added."
3267,10.1016/j.bbagen.2005.12.016,something_else,Cells were seeded in 12-well dishes at a density o ... iability was monitored using trypan blue staining.
3268,10.1016/j.bbagen.2005.12.016,something_else,"Peptides were synthesised (Dr. M. Pitkeathley, Dys ... WSM) over a wide concentration range (1 nM-10 μM)."
3269,10.1016/j.fuproc.2015.01.011,something_else,Characterization of extra-framework species of ste ...  washed faujasite by MQMAS NMR and IR measurements
3270,10.1016/j.fuproc.2015.01.011,something_else,Surface analysis by XPS spectroscopy was applied t ... /Lorentzian ratio for peak decomposition was used.
3271,10.1016/j.fuproc.2015.01.011,something_else,"IR spectroscopy of adsorbed pyridine was used to p ... nts of 0.73 cm/mol 1.11 cm/mol, respectively [27]."
3272,10.1016/j.fuproc.2015.01.011,something_else,High resolution transmission electron microscopy ( ...  and dispersed over a carbon coated holey Cu grid.
3273,10.1016/j.fuproc.2015.01.011,something_else,"NH4-Y zeolite with sodium content less than 0.15 w ...  were 1 wt% of P, 15 wt% of MoO3 and 3 wt% of NiO."
3274,10.1016/j.apsusc.2005.12.010,something_else,Specimens were cut from n-type Si (0 0 1) and Si ( ... TM system [25] to observe their surface structure.
3275,10.1016/j.matlet.2007.03.047,something_else,The samples were mounted on a water-cooled copper  ... e pyrometer was insensitive to the flame emission.
3276,10.1016/j.matlet.2007.03.047,something_else,Diamond crystallites and/or continuous polycrystal ...  taken primarily from the scratched Si substrates.
3277,10.1002/app.26086,something_else,DSC thermograms obtained for MDI-modified TPU. The ... esulting gel contents of the sample are indicated.
3278,10.1002/app.26086,something_else,"DSC thermograms obtained for unmodified TPU sample ... Ta = 50-100degC, ta = 15 min, and +q = 10degC/min."
3279,10.1002/app.26086,something_else,DSC isothermal traces of the TPUs during annealing ... 15 min. Only the first 3 min are represented here.
3280,10.1002/app.26086,something_else,The TPU and the polyisocyanate (MDI or tIPDI) were ... vation between the different steps of the process.
3281,10.1002/app.26086,something_else,"After this first characterization, different therm ... underwent a second heating ramp at the rate of +q."
3282,10.1002/app.26086,something_else,A Pyris 1 differential scanning calorimeter (Perki ... btracted from the heat flow of the studied sample.
3283,10.1016/j.matlet.2007.03.047,something_else,More detailed studies of the complete range of gro ... s and increase the area of uniform film thickness.
3284,10.1016/j.jphotochem.2014.11.021,something_else,The photoactivity was tested by means of the degra ... nged during the photodegradation tests (pH ~ 6.5).
3285,10.1002/jctb.4282,something_else,Lignin obtained from black liquor was supplied by  ... the solutions were prepared using deionized water.
3286,10.1002/jctb.4282,something_else,"After the degradation of lignin, the reactant liqu ... , 105(20), 91(19), 79(26), 65(16), 57(17), 41(25)."
3287,10.1016/j.tsf.2014.12.017,something_else,"Cu(In, Ga)Se2 thin films and solar cells prepared by selenization of metallic precursors"
3288,10.1016/j.tsf.2014.12.017,something_else,Selenization process (Fig. 3) was started with an  ... rocesses were used for CIGS thin film preparation.
3289,10.1016/j.tsf.2014.12.017,something_else,The bilayers were selenized in a quartz tube furna ... ubbers containing an aqueous solution of 3 M NaOH.
3290,10.1016/j.tsf.2014.12.017,something_else,"First, 0.8-0.9 μm thick Mo back contact layer was  ... s were made without intentional substrate heating."
3291,10.1016/j.tsf.2014.12.017,something_else,Phenylselenocarboxamide was synthesized by a react ... ecommend handling the precursor under a fume hood.
3292,10.1016/j.tsf.2014.12.017,something_else,Phenylselenocarboxamide synthesized in this study  ... sorbers prepared by using phenylselenocarboxamide.
3293,10.1016/j.fuproc.2011.03.011,something_else,"In a typical experiment, 0.6-1.0 g of fresh cataly ...  from the total mass balance of carbon conversion."
3294,10.1016/j.fuproc.2011.03.011,something_else,The amount of H2 chemisorbed was determined for th ...  and then cooled down to 100 degC before analyses.
3295,10.1002/jctb.4282,something_else,Sodium hydroxide (0.5 mol L-1) solution was used t ...  cm-2 for a duration of 0-5 h at room temperature.
3296,10.1016/j.fuproc.2011.03.011,something_else,The structures of MS-X and HS-X supports and the f ... ed with carbon film and dried at room temperature.
3297,10.1002/adma.201000599,something_else,The Fe70Pd30 films were deposited in a Von Ardenne ... ion rate of 0.024 nm s-1 at 30 W sputtering power.
3298,10.1111/j.1151-2916.1964.tb14441.x,something_else,"*Li2CO3 was Fisher-certified reagent grade, GeOe w ...  electronic grade from Allied Chemical Corporation"
3299,10.1016/j.matchemphys.2016.05.032,something_else,"Two nanocrystalline FINEMET samples, here denoted  ... ic field. The thickness of the ribbons was ~20 μm."
3300,10.1002/jctb.4282,something_else,Anodic oxidation as green alternative for removing ... e from wastewater using Pb/PbO2 and Ti/SnO2 anodes
3301,10.1002/jctb.4282,something_else,"In this study, a new process was developed and inv ...  reaction time 3 h and current density 25 mA cm-2."
3302,10.1002/jctb.4282,something_else,"At the end of the electrochemical degradation, the ... ctural components in the unreacted lignin residua."
3303,10.1002/jctb.4282,something_else,Nyquist plots of the Pb/PbO2 electrodes recorded i ...  for 10 min with current density of 10-40 mA cm-2.
3304,10.1002/jctb.4282,something_else,"Semi-preparative HPLC (SHIMADIU, GC-2010) equipped ... tention times 27.4 min and 36.3 min, respectively."
3305,10.1016/j.fuproc.2011.03.011,something_else,In order to investigate the effect of diffusion in ...  350 degC for 4 h at a heating rate of 1 degC/min.
3306,10.1016/j.chroma.2014.07.058,something_else,The linearity of the method was determined by anal ... ch enantiomer of cis-epoxiconazole and indoxacarb.
3307,10.1016/j.chroma.2014.07.058,something_else,"For this analysis, a 5.00 +- 0.01 g sample was ini ... ent procedures as that described in Section 2.3.1."
3308,10.1016/j.chroma.2014.07.058,something_else,Finely homogenized made tea samples (2.00 +- 0.01  ... trix-matched external standard calibration method.
3309,10.1007/s10800-010-0139-1,something_else,The electrochemical experiments were carried out u ... eriments was a 0.5 mol L-1 H2SO4 aqueous solution.
3310,10.1016/j.jnucmat.2006.02.083,something_else,"From the irradiated specimens M1-I3 and M2-I2, sli ... ied to the individual slices are given in Table 3."
3311,10.1016/j.jpowsour.2003.11.023,something_else,In order to investigate the deposition behavior wi ... he corresponding concentration is kept at 2 g l-1.
3312,10.1016/j.jpowsour.2003.11.023,something_else,Effect of YSZ concentration in sensitization bath  ... ) YSZ concentration in electroless bath (8 g l-1).
3313,10.1016/j.jpowsour.2003.11.023,something_else,In order to study the effect of concentration of p ... is formed [18] and [19] by the following reaction:
3314,10.1016/j.jpowsour.2003.11.023,something_else,"In order to initiate electroless plating on insula ... he time of deposition, on the deposition kinetics."
3315,10.1016/j.jpowsour.2003.11.023,something_else,"YSZ powder (8 mol%) (TZ-8Y, Tosoh Corporation, Jap ... echnique using a 7.5-digit multi-meter (HP 3458A)."
3316,10.1016/j.jcis.2009.04.060,something_else,Two-step growth was also performed following the s ... egC and then hot stirring was carried out for 5 h.
3317,10.1016/j.apcatb.2009.03.019,something_else,"Photodegradation of phenol was carried out by prep ...  coefficient r2 = 0.9777, and a slope eb = 1363.7."
3318,10.1016/j.apcatb.2009.03.019,something_else,The adsorption capacity of calcined LDHs was deter ... ere taken from the solutions every 30 min for 6 h.
3319,10.1016/j.jnucmat.2008.10.027,something_else,"An INSTRON 5566 testing machine, equipped with a 5 ... TRON 3119 furnace was used for the 350 degC tests."
3320,10.1016/j.jpowsour.2005.03.043,something_else,The Sn-Ni thin films with different composition we ... r atmosphere (dew point was kept under -100 degC).
3321,10.1016/j.tetlet.2014.06.065,something_else,General procedure for the synthesis of β-(methylth ... l using ethyl acetate-pet ether (5:95) as eluents.
3322,10.1016/j.tetlet.2014.06.065,something_else,"Reaction conditions: Chloroacrolein (10 mmol), DDC ...  heated at 90 degC for 1-2 h (monitored by TLC).10"
3323,10.1016/j.tetlet.2014.06.065,something_else,Reaction conditions: POCl3 (15 mmol) was added dro ... mixture is basic and heated to 90 degC for 45 min.
3324,10.1016/j.msea.2014.09.005,something_else,The microstructure and fracture morphology of the  ... perchloric acid and 95% alcohol at about -20 degC.
3325,10.1016/j.msea.2014.09.005,something_else,A kind of ultra-high strength dual-phase steel und ... tment system. All these steps are shown in Fig. 1.
3326,10.1016/j.apcatb.2009.03.019,something_else,"Photodegradation of 2,4-d was carried out by prepa ... ithout filter, which was immersed in the solution."
3327,10.1016/j.ces.2013.04.029,something_else,"EC studies were carried out using the experimental ... ssolution of the floc, aluminum was also analyzed."
3328,10.1016/j.jcis.2009.04.060,something_else,Precipitates of the washed colloidal suspensions w ... measurements were carried out at room temperature.
3329,10.1016/j.jcis.2009.04.060,something_else,Optical reflectance spectra of ZnO rods prepared i ... rption was studied using reflectance measurements.
3330,10.1016/j.tet.2008.06.089,something_else,"Route b. The general procedure for the synthesis o ... d DPPA to afford 63 (20 mg, 88%) as colorless oil."
3331,10.1016/j.tet.2008.06.089,something_else,"Route a. The general procedure for the synthesis o ... 0.7, CHCl3); IR (neat, cm-1) 1738 (CO), 3328 (NH)."
3332,10.1016/j.tet.2008.06.089,something_else,"To the solution of carbamate 60 in dichloromethane ... 2.9, CHCl3); IR (neat, cm-1) 1707 (CO), 3288 (NH)."
3333,10.1016/j.tet.2008.06.089,something_else,"Compound 60 was dissolved in methanol, THF, and H2 ... 2.5, CHCl3); IR (neat, cm-1) 1710 (CO), 3280 (NH)."
3334,10.1016/j.tet.2008.06.089,something_else,"To the mixture of carboxylic acid 58 (38 mg, 0.066 ... .75, CHCl3); IR (neat, cm-1) 1705 (CO), 3284 (NH)."
3335,10.1016/j.tet.2008.06.089,something_else,"To the solution of carbamate 26 in dichloromethane ... CH3OH); IR (neat, cm-1) 1711 (CO), 3738-3030 (OH)."
3336,10.1016/j.tet.2008.06.089,something_else,"To the mixture of carboxylic acid 9 (38 mg, 0.066  ... .55, CHCl3); IR (neat, cm-1) 1721 (CO), 3285 (NH)."
3337,10.1016/j.tet.2008.06.089,something_else,"To the solution of 14 (305 mg, 0.536 mmol) in DMF  ...  -1.41 (c 1.35, CHCl3); IR (neat, cm-1) 1730 (CO)."
3338,10.1016/j.jcis.2009.04.060,something_else,(a) XRD patterns of products prepared in aqueous s ... s with different SDS concentrations at pH of 13.5.
3339,10.1016/j.tet.2008.06.089,something_else,"To the solution of 4 (524 mg, 0.944 mmol) in CH3CN ... -9.70 (c 0.26, CHCl3); IR (neat, cm-1): 1734 (CO)."
3340,10.1016/j.tet.2008.06.089,something_else,Now we established the synthetic methodology of ca ... nt using α- and β-sugar carboxylic acids 9 and 10.
3341,10.1016/j.tet.2008.06.089,something_else,"Then, we embarked on the synthesis of a sugar dend ...  of unique dendritic molecule having a sugar core."
3342,10.1016/j.tet.2008.06.089,something_else,"We started this synthetic method at obtaining the  ... 9-14 derived from glucose, galactose, and mannose."
3343,10.1002/anie.201006014,something_else,The catalytic performances of the catalysts were e ...  finished until the soot was completely burnt off.
3344,10.1002/anie.201006014,something_else,The synthesis of 3DOM Aun/LaFeO3 catalysts was car ... C to obtain the desired 3DOM Aun/LaFeO3 catalysts.
3345,10.1002/anie.201006014,something_else,"[a] Conditions: 5 % O2 and 0.2 % NO in Ar, 50 mL m ... e mass ratio (catalyst/soot) is 10:1. [b] Ref. 6a."
3346,10.1016/j.cattod.2006.05.015,something_else,The samples obtained were characterized using X-ra ... ain 2 wt.% of soot in a flow of air (20 mL min-1).
3347,10.1111/j.1151-2916.2001.tb00899.x,something_else,The objectives of this work were to investigate th ... ies obtained from various processes were compared.
3348,10.1016/j.tet.2008.06.089,something_else,"Infrared (IR) spectra were measured on a Jasco FT/ ... hy was performed using SiO2 (Wakogel C-300, Wako)."
3349,10.1016/j.tet.2008.06.089,something_else,"The general procedure for the deprotection of carb ... .6 (c 0.92, H2O); IR (neat, cm-1) 1717 (CO), 3326."
3350,10.1016/j.ces.2013.04.029,something_else,Fig. 1 shows a schematic of the experimental set-u ... ecipitated and the clarified solution is analyzed.
3351,10.1002/app.25820,something_else,"Tested with 50 mg of the polymers in 1 ml of the s ...  25degC for 12 h; -, insoluble at 25degC for 12 h."
3352,10.1016/j.actamat.2008.06.013,something_else,Initial alloy ingots having compositions Nd2Fe82B6 ... Pr = 12 x 10-12 J m-1 for the Pr2Fe14B phase [12].
3353,10.1016/j.elecom.2015.03.018,something_else,Smart bandage biosensors were fabricated by screen ... rop coated with 3 μL of 0.5 wt% chitosan solution.
3354,10.1016/j.elecom.2015.03.018,something_else,"All chemicals were from Sigma-Aldrich (St. Louis,  ... blet. The electronics is described elsewhere [27]."
3355,10.1016/j.tsf.2015.01.036,something_else,A poly(methyl methacrylate) (PMMA) based transfer  ... isopropanol and then rinsing with deionized water.
3356,10.1016/j.tsf.2015.01.036,something_else,"For MoS2 CVD growth, MoO3 (99.999% purity) and S ( ... exposed to a flow of 500-sccm N2 for fast cooling."
3357,10.1016/j.materresbull.2011.12.027,something_else,Transmission electron microscopy (TEM) was carried ...  carbon-coated copper grid and left to dry in air.
3358,10.1016/j.micromeso.2006.02.005,something_else,Ti-PILC has a considerably larger interlayer spaci ... rsors in pillaring agent preparation is promising.
3359,10.1016/j.applthermaleng.2014.08.050,something_else,"In this experimental circuit, the pipe diameter of ... rking fluid via a brazed flat plat heat exchanger."
3360,10.1007/s11148-016-9885-x,something_else,"- synthetic diamond micropowder grade ACM 3/1, syn ... raction from 1 to 3 μm, perfect crystal structure;"
3361,10.1007/s11148-016-9885-x,something_else,More than 80% of titanium carbide in industry is p ...  of TiC in a vacuum is a low productivity process.
3362,10.1016/j.actamat.2016.10.063,something_else,"In the current study, the material used was rolled ...  solution of 10% perchloric acid and 90% methanol."
3363,10.1016/j.cej.2007.11.012,something_else,"The synthetic wastewater was prepared with distill ... e experiments, oxygen was used as the working gas."
3364,10.1016/j.apcata.2007.06.019,something_else,"Reaction conditions: 20 mass% reactant aqueous sol ... D, propanediol; PO, propanol; EG, ethylene glycol."
3365,10.1016/j.apcata.2007.06.019,something_else,Effect of the recycle use of the catalysts on the  ...  = ethylene glycol + ethanol + methanol + methane.
3366,10.1016/j.apcata.2007.06.019,something_else,The tests of the glycerol hydrogenolysis over h-Ru ... re rather stable at reaction temperature of 453 K.
3367,10.1016/j.apcata.2007.06.019,something_else,Dependence on h-Ru/C amount of the glycerol hydrog ...  = ethylene glycol + ethanol + methanol + methane.
3368,10.1007/s11148-016-9885-x,something_else,Synthesis of titanium carbide was performed in a q ...  the reaction product was extracted after cooling.
3369,10.1016/j.ces.2013.04.029,something_else,"Removal of arsenic from large volumes of water is  ... , Hernandez et al., 2010 and Mohora et al., 2012)."
3370,10.1016/j.micromeso.2006.02.005,something_else,The main aim of the present work is to prepare Ti- ... table for shape selective organic transformations.
3371,10.1016/j.micromeso.2006.02.005,something_else,Benzene (Qualigens) and ethanol (Merck) are used a ... product selectivity (weight percentage) are noted.
3372,10.1002/app.25820,something_else,The solubility of PAEK copolymers was examined in  ... les to diffuse easily into the copolymer chains.15
3373,10.1002/app.25820,something_else,Several PAEK copolymers with different composition ...  wt % and the yields were all higher than 90 wt %.
3374,10.1002/app.25820,something_else,The weight loss fractions were obtained by extract ... rotated velocity of the goniometry was 4deg min-1.
3375,10.1002/app.25820,something_else,Fluorobenzene (Liaoning Zhonghe Fine Chemical Plan ... ected and stored over molecular sieves (Type 4 Å).
3376,10.1002/adsc.201500319,something_else,An interesting example of enantioselective conjuga ... the reactions presented in Scheme 66 to Scheme 69.
3377,10.1016/j.actbio.2013.03.017,something_else,"The Zr content is low (~0.03 wt.%) in the middle p ...  metallic Zr particles will form, grow and settle."
3378,10.1016/j.actbio.2013.03.017,something_else,Weight loss tests were performed in a cell culture ... r year (mm y-1) using the following equation [37]:
3379,10.1016/j.actbio.2013.03.017,something_else,Hardness measurements were carried out using a Vic ... of three specimens were tested for each condition.
3380,10.1016/j.micromeso.2006.02.005,something_else,Pillaring is done on montmorillonite KSF (Aldrich) ... th M and NM are also calcined at 500 degC for 5 h.
3381,10.1016/j.actbio.2013.03.017,something_else,"Mg-10(Dy + Gd)-0.2Zr alloys were designed, and the ... 00 degC for various times followed by air cooling."
3382,10.1016/j.jmatprotec.2006.07.023,something_else,"Fretting tests were carried out on a serve-hydraul ... els are listed in Table 1 ; Table 2, respectively."
3383,10.1016/j.renene.2014.02.037,something_else,"FAMEs were quantified directly in GC equipped with ... Supelco, USA) was used as the standard for GC-FID."
3384,10.1016/j.renene.2014.02.037,something_else,Scanning electron microscopy (SEM) experiments wer ... tering to allow a better conduction of the sample.
3385,10.1016/j.renene.2014.02.037,something_else,In the conventional method (M1) the extracted alga ... ined after both the stages of transesterification.
3386,10.1016/j.renene.2014.02.037,something_else,Eight different transesterification methods were c ... terification efficiency was calculated as follows:
3387,10.1016/j.renene.2014.02.037,something_else,Seed culture of Chlorella sp. FC2 IITG [16] and Ch ... otoautotrophic biomass of C. sorokiniana FC6 IITG.
3388,10.1016/j.renene.2014.02.037,something_else,"This study demonstrates a direct transesterificati ... nd hence, could be an alternative to petro-diesel."
3389,10.1016/j.micromeso.2006.02.005,something_else,The present study introduces titania sol prepared  ... ange the pH of sol making the sol unstable in KSF.
3390,10.1016/j.jmatprotec.2006.07.023,something_else,The preparation process of the three coatings (MoS ... s were cleaned with acetone before fretting tests.
3391,10.1016/j.apcata.2007.06.019,something_else,"Hydrolysis of methyl acetate over ion-exchange res ... ure, 2 h reaction time, 700 μmol H+ in the resins."
3392,10.1016/j.tet.2008.06.089,something_else,"To the mixture of carboxylic acid 10 (671 mg, 1.24 ... 52, CHCl3), IR (neat, cm-1): 1748 (CO), 3385 (NH)."
3393,10.1016/j.tet.2008.06.089,something_else,"To the solution of 67 (43 mg, 0.017 mmol) in dichl ... 19 (c 0.42, H2O); IR (neat, cm-1) 1746 (CO), 3317."
3394,10.1016/j.electacta.2008.02.081,something_else,"KCl, KH2PO4, and KH2PO4 were all purchased from Al ... ents were all done at room temperature and in air."
3395,10.1002/anie.200503479,something_else,General procedure: The heteroarylboronic acid (1.1 ... n purified by column chromatography on silica gel.
3396,10.1016/j.jpowsour.2016.02.067,something_else,"Thermogravimetric analysis (TGA, Q50, TA Instrumen ...  heating rate of 10 degC min-1 during the process."
3397,10.1016/j.jpowsour.2016.02.067,something_else,The electrodes used to measure the electrochemical ... ing mode has been given in supplementary material.
3398,10.1002/app.25829,something_else,"After the polymerization, the Mag-H catalyst was r ... no delamination of the clay was observed (Fig. 5)."
3399,10.1002/app.25829,something_else,Polymerizations were performed in acetonitrile at  ... ce (NMR) analysis (yield of this example was 92%).
3400,10.1002/app.25829,something_else,"The clay, which has been used as catalyst, is supp ... 20M, Mag-H+ 0.25M, Mag-H+ 0.30M, and Mag-H+ 0.35M."
3401,10.1002/app.25829,something_else,"2,4,4-trimethyl-2-oxazoline (TMOX) (Aldrich, Franc ...  distillation over their respective drying agents."
3402,10.1016/j.electacta.2008.02.081,something_else,The PBV thin-films were potentiostatically electro ... he residual bath solutions and then stored in air.
3403,10.1002/adma.200903696,something_else,Graphite oxide was prepared by oxidizing graphite  ... to bulk quantities of few-layered graphene sheets.
3404,10.1002/adma.200903696,something_else,In order to disperse the graphene sheets on a subs ... ore smoother in comparison to the graphene-A film.
3405,10.1002/adma.200903696,something_else,The wetting of graphene films from superhydrophobi ... ve proportion of acetone and water in the solvent.
3406,10.1111/cbdd.12569,something_else,"The two primary hydroxyls of α,α-D-trehalose were  ...  to generate the brartemicin amide analogues 8a-m."
3407,10.1111/cbdd.12569,something_else,"Synthesis of the target compounds 8a-m. Reagents a ... CH2Cl2, 0 degC, 2 h; (f) 30% MeONa,/MeOH, rt, 5 h."
3408,10.1111/cbdd.12569,something_else,MDA-MB-231 cells (3 x 105) seeded in 6-well plates ... USA). β-Actin was employed as an internal control.
3409,10.1111/cbdd.12569,something_else,"Activity of MMP-9 in MDA-MB-231 cells was estimate ...  XRS+ image analyzer (Bio-Rad, Hercules, CA, USA)."
3410,10.1111/cbdd.12569,something_else,MDA-MB-231 cells: Invasion assay was performed usi ... erature and then stained with 0.1% crystal violet.
3411,10.1111/cbdd.12569,something_else,Colon 26-L5 cells: Invasion of tumor cells through ... ifferent fields of each well under the microscope.
3412,10.1002/adma.200903696,something_else,"Natural graphite flakes with an average diameter o ... ed from Fuchen Chemical Reagents (Tianjin, China)."
3413,10.1111/cbdd.12569,something_else,MDA-MB-231 cells were seeded in 6-well plates unti ... o get a prototypical result of the entire scratch.
3414,10.1016/j.jeurceramsoc.2009.01.002,something_else,"Three nanostructured coatings with a thickness of  ... d wheel saw cutoff machine (MTI Corporation, USA)."
3415,10.1016/j.matlet.2014.12.039,something_else,"GC-MS spectrum of the pure indium particles treate ... 0201D, GC; He, 40.8 ml/min., 50-250C, MS; EI, pos."
3416,10.1016/j.chroma.2014.07.058,something_else,Fresh tea leaves and soil samples from trial plots ... in the refrigerator below -18 degC until analysis.
3417,10.1016/j.chroma.2014.07.058,something_else,A simultaneous enantiomeric analysis of cis-epoxic ... 0 min. The column temperature was kept at 40 degC.
3418,10.1016/j.chroma.2014.07.058,something_else,Standard stock solutions (200 mg/L) of racemic cis ...  stored in a refrigerator in the dark at -20 degC.
3419,10.1016/j.chroma.2014.07.058,something_else,The 0.2%0 TFA and 2 mmol/L AMF aqueous solution wa ... hina) followed by ultrasonic degassing before use.
3420,10.1016/j.chroma.2014.07.058,something_else,"The cleanup of the used florisil and GCB mixture c ... d with 10 mL hexane/acetone (7/3, v/v) before use."
3421,10.1016/j.chroma.2014.07.058,something_else,"BondElut C18 cartridges (500 mg/6 mL) were purchas ... r (5%, m/m) and storage in a desiccator until use."
3422,10.1016/j.chroma.2014.07.058,something_else,"Racemic cis-epoxiconazole standard (purity at 98%) ... eagent & H.V Chemical Co., Ltd. (Shanghai, China)."
3423,10.1002/anie.200601752,something_else,Fluorescence microscopy imaging of ruthenium-induc ... this addition and d)-f) after the indicated times.
3424,10.1016/j.matlet.2014.12.039,something_else,Pure indium particles were prepared by the convent ... the particle without treatment is shown in Fig. 2.
3425,10.1002/anie.200601752,something_else,Influence of cell extract on the ruthenium-catalyz ...  (1:1) and excited with a long-wavelength UV lamp.
3426,10.1016/j.solmat.2008.11.001,something_else,Bulk heterojunction ITO/PEDOT-PSS/P3HT:PCBM/AL sol ...  on a hot plate at 155 degC for a period of 5 min.
3427,10.1016/j.solmat.2008.11.001,something_else,"For preparation of solar cells, we used regio-regu ...  PCBM blending content was varied from 25% to 50%."
3428,10.1016/j.cemconres.2009.12.007,something_else,The effect of alkali types in cement on the alkali ... ing the risk of underestimating the alkali levels.
3429,10.1016/j.cemconres.2009.12.007,something_else,The predicted concentrations of Na+ and K+ with th ... lue (0.38 mL/g) used by Brouwers and Van Eijk [3].
3430,10.1016/j.cemconres.2009.12.007,something_else,A possible explanation for the different observati ... observed in the experiments of Stade [17] as well.
3431,10.1007/s10854-015-2779-8,something_else,All the samples had a Ta/[NiFe/NiFeO]10/Ta structu ...  microstrip transmission-line perturbation method.
3432,10.1016/j.msea.2007.10.069,something_else,To examine the forging ability of the ECAPed 6061  ... ssed pancake by imposing a load of 100 g for 15 s.
3433,10.1016/j.msea.2007.10.069,something_else,The conventionally extruded 6061 Al alloy rods wit ... tailed ECAP procedures are provided elsewhere [4].
3434,10.1002/anie.200601752,something_else,"In the course of screening several organometallic  ... s a secondary amine (2 d, 87 % yield; Scheme 1).13"
3435,10.1016/j.tet.2008.06.089,something_else,"To the solution of 66α (14 mg, 0.01 mmol) in dichl ... 53, CHCl3); IR (neat, cm-1): 1746 (CO), 3325 (NH)."
3436,10.1111/cbdd.12569,something_else,MDA-MB-231 cells were seeded in 96-well plates at  ... te experiments with sixfold sample were performed.
3437,10.1111/cbdd.12569,something_else,Murine colon 26-L5 carcinoma cells were cultured i ... ic acid and the absorbance at 590 nm was measured.
3438,10.1016/j.bbr.2003.10.011,something_else,Phenyl acetate (Aldrich Chemicals) and linalool (A ... sample (0.01 ml) was used for each training trial.
3439,10.1016/j.electacta.2006.08.060,something_else,"Silicon (1 1 1) wafers (0.5-5.0 Ω cm, n-type, Virg ... nd obtain hydrogen-terminated silicon (Si-H) [27]."
3440,10.1016/j.electacta.2006.08.060,something_else,All chemicals were of reagent or the highest avail ... fied by passing through an activated Al2O3 column.
3441,10.1016/j.micromeso.2006.02.004,something_else,"In the preparation procedure of catalysts I, a vol ... o the oxygen activation treatment described above."
3442,10.1016/j.micromeso.2006.02.004,something_else,Catalysts A were prepared by solid-state reaction  ... g rate: 5 degC min-1) and 1 h at that temperature.
3443,10.1016/j.micromeso.2006.02.004,something_else,"Two series of three samples were prepared, one by  ... y with the A series with increasing Co/Al content."
3444,10.1016/j.jeurceramsoc.2010.11.001,something_else,Polyacryl tubes with an inner diameter of 20 mm we ... ent height and the initial particle concentration.
3445,10.1016/j.jeurceramsoc.2010.11.001,something_else,"The slurry was centrifuged (Hettich Co., Ltd., EBA ... measured in the supernatant from the added amount."
3446,10.1016/j.bbr.2003.10.011,something_else,"The odour was presented on filter paper (Whatman n ... nt, the sugar (~0.05 g) was buried in the bedding."
3447,10.1016/j.jeurceramsoc.2010.11.001,something_else,"In this paper, the effects of sintering additives  ...  in terms of the sediment packing volume fraction."
3448,10.1002/aic.14312,something_else,"The I-V polarization test of the tubular SC-SOFCs  ... -1, O2: 150 mL min-1) was applied as the feed gas."
3449,10.1002/aic.14312,something_else,The flow-through tubular cells applied in this stu ...  firmly after the calcination at 1000degC for 2 h.
3450,10.1016/j.matlet.2006.06.068,something_else,"Appropriate resin, ratio of spherical copper and f ... rage adhesion strength of the electrode is 6.8 lb."
3451,10.1016/j.matlet.2006.06.068,something_else,"Resin, copper powder and glass were mixed to prepa ...  a controlled level of oxygen, to obtain BME-MLCC."
3452,10.1016/j.matlet.2006.06.068,something_else,"All chemicals of reagent grade quality were used w ...  from the solution, washed and dried under vacuum."
3453,10.1016/j.jeurceramsoc.2017.01.003,something_else,A Setaram Setsys 16/18 vertical dilatometer (Setar ... . (1) to evaluate the β-SiC crystallite size [31]:
3454,10.1016/j.tet.2008.06.089,something_else,"To the solution of carbamate 72 in dichloromethane ... ; IR (neat, cm-1) 1559, 1649 (CO), 3580-3060 (OH)."
3455,10.1016/j.tet.2008.06.089,something_else,"To the solution of carboxylic acid 9 (28 mg, 0.048 ... HCl3); IR (neat, cm-1) 1562, 1651 (CO), 3275 (NH)."
3456,10.1002/aic.14312,something_else,Comparative study of doped ceria thin-film electro ... praying with powder synthesized via two techniques
3457,10.1111/cbdd.12569,something_else,MDA-MB-231 human breast adenocarcinoma cells (ATCC ... ate density according to each experimental design.
3458,10.1016/j.bbr.2003.10.011,something_else,Odour discrimination tests were performed the day  ... ile the apparatus was prepared for the test phase.
3459,10.1016/j.bbr.2003.10.011,something_else,The animals were deeply anaesthetised with sodium  ...  within the olfactory bulb of each animal's brain.
3460,10.1111/cbdd.12569,something_else,Dulbecco's modified Eagle's minimal essential medi ... was obtained by the in vivo selection method [37].
3461,10.1111/cbdd.12569,something_else,"To a solution of 7a (126 mg, 0.11 mmol) in anhydro ... for C26H33N2O11 [M + H]+ 549.2079, found 549.2085."
3462,10.1111/cbdd.12569,something_else,"To a solution of benzoic acid (60 mg, 0.48 mmol) a ... or C68H57N2O17 [M + H]+ 1173.3652 found 1173.3651."
3463,10.1111/cbdd.12569,something_else,"A solution of 5 (13.8 g, 13.58 mmol) in EtOAc (200 ... 0 (dd, J = 7.2, 12.6 Hz, 1H); ESI-MS 965 [M + H]+."
3464,10.1111/cbdd.12569,something_else,"Under an N2 atmosphere, a stirred mixture of the m ... or C54H45N6O15 [M + H]+ 1017.2937 found 1017.2941."
3465,10.1111/cbdd.12569,something_else,To a stirred solution of 3 (16.0 g) in anhydrous C ... or C56H51O21S2 [M + H]+ 1123.2359 found 1123.2362.
3466,10.1111/cbdd.12569,something_else,To a clear solution of trehalose dihydrate (10.0 g ... d. for C54H47O17 [M + H]+ 967.2808 found 967.2810.
3467,10.1111/cbdd.12569,something_else,Melting points were determined on an X-6 micromelt ... from sodium/benzophenone immediately prior to use.
3468,10.1016/j.bbr.2003.10.011,something_else,"For the testing phase, rose and lemon odours were  ... tus was rotated 180deg after testing each subject."
3469,10.1016/j.jcat.2013.08.018,something_else,The evolution of Pd particles on carbon in vacuum  ... r is referred to the web version of this article.)
3470,10.1016/j.chroma.2014.08.051,something_else,"The experiments denoted with UHPLC were performed  ... , were 0.096 and 0.112 mL for the two BEH columns."
3471,10.1016/j.chroma.2014.08.051,something_else,"Solutions of BTEAC, C7 and SNS were prepared by di ... purchased from Whatman (Maidstone, UK) before use."
3472,10.1016/j.chroma.2014.08.051,something_else,"The mobile phase consisted of gradient grade aceto ... traZeneca (Molndal, Sweden), were used as solutes."
3473,10.1016/j.electacta.2007.02.022,something_else,"After the substrate was placed in the cell, it was ... h position permitted ORR imaging of the substrate."
3474,10.1016/j.electacta.2007.02.022,something_else,Pt stripes were characterized for their electroche ...  solution of 0.01 M H2SO4/0.1 M Na2SO4 before use.
3475,10.1016/j.electacta.2007.02.022,something_else,"Thin metal stripes were prepared by plasma sputter ... ed, as it depends on defining a cut-off thickness."
3476,10.1016/j.bbr.2003.10.011,something_else,Odour stimuli and training and testing chambers we ... es were similar to those outlined in Experiment 1.
3477,10.1016/j.bbr.2003.10.011,something_else,Sections prepared for immunohistochemistry were im ...  50% glycerol solution 0.024% p-phenylenediamine).
3478,10.1002/pola.1988.080261103,something_else,Novel phenyl-pendant aromatic polythiazoles having ...  10% weight loss being recorded at around 570degC.
3479,10.1016/j.fuel.2014.12.018,something_else,Nahcolite and dawsonite content were measured by m ... e traditional water-then-HCl leaching method [14].
3480,10.1016/j.fuel.2014.12.018,something_else,"Core slabs 0.6-m-long were crushed, homogenized, a ... by digestion followed by either ICP-AES or ICP-MS."
3481,10.1016/j.ijhydene.2007.09.007,something_else,A custom-made cathodic vacuum arc deposition syste ... was maintained at 70 A during the coating process.
3482,10.1016/j.conbuildmat.2012.12.059,something_else,"Table 6 and Fig. 4 and Fig. 5, which display the f ... , the lower the flexural and compressive strength."
3483,10.1016/j.conbuildmat.2012.12.059,something_else,"Li2SO4, LiNO3, Li2CO3, and LiBr were added into th ... hmetic average was recorded as compressive stress."
3484,10.1016/j.conbuildmat.2012.12.059,something_else,"Aggregate, water and cement used for the ASR were  ... re applied water cure for 28 days at 20 +- 3 degC."
3485,10.1016/j.conbuildmat.2012.12.059,something_else,Lithium salts were added to the cement paste at th ... assessed according to TS EN 196-3 guidelines [31].
3486,10.1016/j.conbuildmat.2012.12.059,something_else,"Mortar bar experiment method accelerated according ... ion, and their lengths were recorded periodically."
3487,10.1016/j.conbuildmat.2012.12.059,something_else,Aim of this study intends analyzing the effects of ... pe (SEM) and Energy Dispersive Spectroscopy (EDS).
3488,10.1016/j.electacta.2008.02.084,something_else,To investigate the influence of applied cathode po ... trodes and conditions used for biotic experiments.
3489,10.1016/j.electacta.2008.02.084,something_else,The cathodic compartment of the bio-electrochemica ... s) was continuously mixed with a magnetic stirrer.
3490,10.1016/j.solmat.2010.12.052,something_else,1H and 13C NMR spectra were recorded using a Bruke ... Q surface profilometer with an accuracy of +-1 nm.
3491,10.1016/j.solmat.2010.12.052,something_else,"Compound 3 (1.0 g, 2.08 mmol) was dissolved in dry ... The 1H NMR spectrum of PTZ-C60 is shown in Fig. 1."
3492,10.1016/j.solmat.2010.12.052,something_else,"Compound 2 (1.0 g, 3.36 mmol) and p-toluenesulfony ... , 47.87, 31.60, 26.94, 26.76, 22.77, 21.80, 14.17."
3493,10.1016/j.solmat.2010.12.052,something_else,"Compound 2 was synthesized from 1 by Vilsmeier for ...  114.99, 48.23, 31.59, 26.94, 26.72, 22.77, 14.17."
3494,10.1016/j.solmat.2010.12.052,something_else,"Phenothiazine (5.0 g, 0.025 mol) and sodium hydrox ...  115.52, 47.55, 31.61, 27.04, 26.79, 22.74, 14.15."
3495,10.1016/j.solmat.2010.12.052,something_else,"Phenothiazine, sodium hydroxide, and hydrochloric  ... cal grade) were used without further purification."
3496,10.1016/j.nanoen.2014.12.040,something_else,Graphene was synthesized using thermal chemical va ... nd 2D peaks were fitted with Lorentzian functions.
3497,10.1016/j.bmcl.2010.08.044,something_else,"Herein, the synthesis, in vitro evaluation and mol ... upplementary data available).13, 14, 15, 16 and 17"
3498,10.1016/j.jelechem.2012.02.011,something_else,"Pb-MnO2 composite coatings were electrochemically  ... nO2 (CMD) of high purity (>95%, Huitong Co. Ltd.)."
3499,10.1016/j.conbuildmat.2012.12.059,something_else,"Among the Li2SO4, LiNO3, Li2CO3 and LiBr added mor ... ) strength was observed in 1% LiNO3 added mortars."
3500,10.1016/j.conbuildmat.2012.12.059,something_else,It was observed that increasing LiNO3 by 3% in LiN ... ressive strength according to reference specimens.
3501,10.1016/j.compositesa.2013.07.019,something_else,"The PR, which was a thermosetting resin, was suppl ... lytical grade from Xi'an Chemical Reagent Factory."
3502,10.1016/j.compositesa.2013.07.019,something_else,"The GOs with different reduction degrees were obta ... mperatures of 120, 200 and 250 degC, respectively."
3503,10.1016/j.tsf.2010.03.152,something_else,"The process chamber with a RPB source was evacuate ... 1 μm and approximately 40% of 17 mW, respectively."
3504,10.1016/j.surfcoat.2013.06.073,something_else,"For observation of the cross-section morphology an ... r 5 min, and finally it was broken off by bending."
3505,10.1016/j.surfcoat.2013.06.073,something_else,The samples with MAO coating were dipped into the  ...  ambient air and then aged at 190 degC for 10 min.
3506,10.1016/j.surfcoat.2013.06.073,something_else,"PP-g-MAH, with the grafting degree of 1-1.2 wt.% a ... nd 10% PP-g-MAH, into dimethylbenzene at 120 degC."
3507,10.1016/j.surfcoat.2013.06.073,something_else,The aluminum sheets were 2 mm thick 2519 aluminum  ... nder pulse voltage mode with 360-400 V for 10 min.
3508,10.1016/j.scriptamat.2004.11.035,something_else,Cu-6 wt.%Ag and Cu-6 wt.%Ag-1 wt.%Cr were molten i ... ion of 99.99% in cross-sectional area of the rods.
3509,10.1016/j.ssc.2009.05.024,something_else,P-type ZnO thin films were synthesized on silicon  ... he dark as well as under UV (350 nm) illumination.
3510,10.1016/j.jorganchem.2006.10.017,something_else,"To a suspension of TmI3(THF)3.5 (0.60 g, 0.75 mmol ... Tm2: C, 32.90; H, 6.63. Found: C, 32.07; H, 6.98%."
3511,10.1016/j.apsusc.2011.08.068,something_else,The DPN system in use here was from NanoInk Inc. I ... his assumption will be discussed with the results.
3512,10.1016/j.jorganchem.2006.10.017,something_else,"To a suspension of TmI3(THF)3.5 (0.85 g, 1.06 mmol ... 3Tm: C, 26.54; H, 5.32. Found: C, 26.50; H, 5.65%."
3513,10.1016/j.jorganchem.2006.10.017,something_else,All manipulations were carried out using standard  ...  were prepared by previously published procedures.
3514,10.1016/j.jcat.2011.03.008,something_else,"Before reaction, we reduced the catalyst in dilute ... to ensure that there was no catalyst deactivation."
3515,10.1016/j.jcat.2011.03.008,something_else,The water gas shift catalysts studied here are com ... will note its composition and relevant properties.
3516,10.1016/j.apcatb.2009.03.010,something_else,The clean Si wafer was then put into the vessel co ... TiO2 could be fabricated by using n-type Si wafer.
3517,10.1016/j.apcatb.2009.03.010,something_else,"Si wafers (n-type Si (1 1 1), phosphorus-doped, an ...  min and drying in argon flow at room temperature."
3518,10.1016/j.compositesa.2013.07.019,something_else,The surfaces of PR and GO/PR composite were coated ... iffractometer with Cu Ka radiation (λ = 0.154 nm).
3519,10.1016/j.compositesa.2013.07.019,something_else,The DSC was performed on a NETZSCH DSC 200PC (NETZ ... ure to 800 degC using a N2 flow rate of 60 mL/min.
3520,10.1016/j.compositesa.2013.07.019,something_else,"The GO/PR composites were prepared by dispersing G ... , and was weight every 30 min till no weight loss."
3521,10.1016/j.jorganchem.2006.10.017,something_else,"To a suspension of YI3(THF)3.5 (1.14 g, 1.58 mmol) ... 58 (SiMe3), 27.04 (THF), 57.84 (OMe), 69.43 (THF)."
3522,10.1016/j.apsusc.2011.08.068,something_else,"In this study, the BSA proteins were 66 kDa obtain ... for the t-aC and a-C:H:Si materials, respectively."
3523,10.1016/j.ijggc.2014.03.001,something_else,"The rich solution, which comes out from the bottom ... .83 GJ/t CO2 and 0.01-0.14 GJ/t CO2, respectively."
3524,10.1016/j.ijggc.2014.03.001,something_else,"Before being introduced into the absorber, flue ga ... e flue gas into the absorber are given in Table 1."
3525,10.1002/ejoc.201300748,something_else,"(+-)-2-(2-Bromo-4,5-dimethoxyphenyl)pyrrolidines ( ... ) Calcd. for C12H17BrNO2 286.0443, found 286.0444."
3526,10.1002/ejoc.201300748,something_else,"(+)-(R)-2-(3,4-Dimethoxyphenyl)pyrrolidine (15): T ... I+) Calcd. for C12H18NO2 208.1338, found 208.1341."
3527,10.1002/ejoc.201300748,something_else,"(+)-(R)-4-(1-Azidobut-3-en-1-yl)-1,2-dimethoxybenz ... r C12H15O2 [M + H - HN3] 191.1072, found 191.1075."
3528,10.1002/ejoc.201300748,something_else,"(+-)-1-(4,5-Dimethoxy-2-vinylphenyl)but-3-en-1-ol  ... r C14H17O2 [M + H - H2O] 217.1229, found 217.1226."
3529,10.1002/ejoc.201300748,something_else,"(-)-(S)-1-(3,4-Dimethoxyphenyl)but-3-en-1-ol (9):  ... +) Calcd. for C12H16NaO3 231.0997, found 231.0997."
3530,10.1002/ejoc.201300748,something_else,General Methods: 1H and 13C NMR spectra were measu ...  with P2O5. Triethylamine was distilled from CaH2.
3531,10.1002/ejoc.201300748,something_else,"Synthesis of S-(-)-crispine A; reagents and condit ...  m) Bu3SnH, cat. AIBN, toluene, reflux, 1 h, 79 %."
3532,10.1002/ejoc.201300748,something_else,"Synthesis of (+)-crispine A; reagents and conditio ... ;g) Bu3SnH, cat. AIBN, toluene, reflux, 1 h, 80 %."
3533,10.1002/ejoc.201300748,something_else,"(+)-tert-Butyl (R)-2-(3,4-Dimethoxyphenyl)pyrrolid ... ) Calcd. for C17H25NNaO4 330.1681, found 330.1681."
3534,10.1002/ejoc.201300748,something_else,"To overcome the unforeseen difficulty in C-C bond  ...  core in very good yield (79 %, de > 90 %).20c,20d"
3535,10.1002/ejoc.201300748,something_else,"Synthesis of 2-aryl pyrrolidines 17 and 18; reagen ...  h, MeOH; d) (Boc)2O, Et3N, THF, 0 degC-r.t., 2 h."
3536,10.1002/ejoc.201300748,something_else,The asymmetric center was thought to be formed by  ... litating structure isolation and characterization.
3537,10.1016/j.msea.2007.11.066,something_else,Stir casting technique is applied to prepare AA606 ... t steel mould. The mould temperature was 250 degC.
3538,10.1016/j.tsf.2010.03.155,something_else,InN and GaN layers were grown on 330 μm thick c-pl ... spects such as growth rate and surface morphology.
3539,10.1016/j.cattod.2011.11.013,something_else,The surface areas of the samples were obtained by  ...  BET equation in 0.05-0.35 partial pressure range.
3540,10.1016/j.cattod.2011.11.013,something_else,"The CeO2-TiO2 and V2O5-WO3/TiO2 catalysts calcined ... CeO2-TiO2-800 and V2O5-WO3/TiO2-800, respectively."
3541,10.1016/j.cattod.2011.11.013,something_else,To comprehensively evaluate the activity of the Ce ... as calcined in air conditions at 550 degC for 6 h.
3542,10.1002/anie.200800585,something_else,"Completion of the total synthesis of 1: a) 6 a, 9- ... abutylammonium fluoride, TFA=trifluoroacetic acid."
3543,10.1002/ejoc.201300748,something_else,"Pd-mediated coupling reactions; reagents and condi ... , refer to Table S1 in the Supporting Information."
3544,10.1016/j.msea.2013.02.010,something_else,The experimental alloy ingot was prepared by casti ...  dimensions of tensile sample are shown in Fig. 1.
3545,10.1002/ejoc.201300748,something_else,"(+-)-tert-Butyl 2-(2-Bromo-4,5-dimethoxyphenyl)pyr ... ) Calcd. for C17H25BrNO4 386.0967, found 386.0970."
3546,10.1002/ejoc.201300748,something_else,"(-)-(2S)-2-(3,4-Dimethoxyphenyl)-1-[2-(phenylsulfi ... hesized in 77 % with [α]D25 = -118 (c = 1, CHCl3)."
3547,10.1016/j.ijggc.2014.03.001,something_else,The baseline MEA-CO2 absorption/desorption process ... hen further purified to yield the CO2 product gas.
3548,10.1016/j.ijggc.2014.03.001,something_else,"Two absorption/stripping process configurations, n ...  equivalent work by 10.7% and 33.9%, respectively."
3549,10.1002/ijc.26463,something_else,All the tissue samples were formalin-fixed and par ... Tris-buffered saline without the primary antibody.
3550,10.1016/j.solmat.2006.07.004,something_else,The photocatalytic degradation of gaseous formalde ... n values of the photocatalytic degradation effect.
3551,10.1016/j.solmat.2006.07.004,something_else,The single-plate and parallel-plate photoreactors  ... ere reported in the previous studies [6] and [17].
3552,10.1016/j.solmat.2006.07.004,something_else,The single-pass circulation test equipment was set ... eactor for simultaneous collection of air samples.
3553,10.1016/j.solmat.2006.07.004,something_else,The visible-light-assisted photocatalytic effect o ... photocatalytic decolorization effect was obtained.
3554,10.1016/j.solmat.2006.07.004,something_else,The DSC and TG analysis were preformed using a NET ... al of the residual organics and chemisorbed water.
3555,10.1002/ejoc.201300748,something_else,"(+)-(2R)-2-(3,4-Dimethoxyphenyl)-1-(2-phenylsulfin ... +) Calcd. for C20H26NO3S 360.1633, found 360.1630."
3556,10.1016/j.solmat.2006.07.004,something_else,A series of characterization tests were conducted  ... dy. The characteristics found are presented below.
3557,10.1016/j.elecom.2015.03.013,something_else,Bulk oxidations were carried out in an undivided e ... ults was evaluated by three independent analyses).
3558,10.1016/j.elecom.2015.03.013,something_else,"A sequence of iodometric titration tests were carr ... hematized by Eqs. (1), (2), (3), (4), (5) and (6)."
3559,10.1016/j.renene.2004.10.013,something_else,The turbine was mounted on a shaft in a cylindrica ... lade chord length was 0.74x105 at peak efficiency.
3560,10.1007/s11661-006-9053-x,something_else,The candidate material selected for the study was  ... lumina powders (grit 600) before being to corrode.
3561,10.1016/j.matdes.2015.07.013,something_else,Iron plate samples of 99.4 wt.% purity with dimens ... rder to prevent oxidation and hydrogen permeation.
3562,10.1002/ejoc.201300748,something_else,"(+)-(R)-8,9-Dimethoxy-1,2,3,5,6,10b-hexahydropyrro ... I+) Calcd. for C14H20NO2 234.1494, found 234.1493."
3563,10.1002/ejoc.201300748,something_else,"(-)-(10bS)-8,9-Dimethoxy-6-(phenylthio)-1,2,3,5,6, ... starting from (-)-19. [α]D25 = -60 (c = 1, CHCl3)."
3564,10.1002/ejoc.201300748,something_else,"(+)-(10bR)-8,9-Dimethoxy-6-(phenylthio)-1,2,3,5,6, ... +) Calcd. for C20H24NO2S 342.1528, found 342.1526."
3565,10.1016/j.solmat.2006.07.004,something_else,Sol-gel TiO2 thin-films were prepared according to ... ing any further modification of the photocatalyst.
3566,10.1016/j.msea.2013.02.010,something_else,"Samples for optical microscope (OM) analysis were  ... 1.74L, where L is the linear intercept grain size."
3567,10.1007/s10853-009-3447-2,something_else,All the reagents were analytical grade and used as ... g and Cu were coated on the surface of the fibers.
3568,10.1007/s10853-009-3447-2,something_else,"Then, 0.07 g of AgNO3 was dissolved in 3 mL of H2O ... action had been kept for 12 h at room temperature."
3569,10.1016/j.jcat.2004.09.008,something_else,A second experiment differed from the first in tha ... entration turns into a decease after about 10 min.
3570,10.1016/j.jcat.2004.09.008,something_else,The Na form of the zeolites (with a molar ratio of ... orresponds to 0.15 to 0.7 molecules per unit cell.
3571,10.1002/smll.200800270,something_else,For the live/dead viability/cytotoxicity assay (In ... immediately viewed with a fluorescence microscope.
3572,10.1002/smll.200800270,something_else,The pEGFP-N1 plasmid DNA was transfected to HeLa c ... n medium was then replaced by DMEM with FBS (10%).
3573,10.1002/smll.200800270,something_else,Cells were washed quickly in PBS and fixed with pa ... roscope was used to observe and record the images.
3574,10.1002/smll.200800270,something_else,The arrayed cover slide was washed twice with phos ... tured at 37 degC in a humidified 5% CO2 incubator.
3575,10.1002/smll.200800270,something_else,"After preparing the cover slide affixed on a glass ... AFM (Digital Instruments, Santa Barbara, CA, USA)."
3576,10.1002/smll.200800270,something_else,Microscope glass cover slides (18 x 18 mm2) were e ... ation chemistry (mPEG-silane) to form PEG brushes.
3577,10.1002/chem.200903035,something_else,We next turned our attention to using the sialyl p ... ccharide 25 was obtained in 30 % yield (Scheme 5).
3578,10.1002/smll.200800270,something_else,"Gold colloids (15-nm, spherical) were synthesized  ... water (100 uL, [?]1012 particles/ml) prior to use."
3579,10.1016/j.apcatb.2014.08.022,something_else,"The concentration of dissolved oxygen in the elect ... pany, Model - HQ440d) immersed in the electrolyte."
3580,10.1016/j.apcatb.2014.08.022,something_else,The performance of our materials for electrochemic ... xperiments were carried out at a room temperature.
3581,10.1016/j.apcatb.2014.08.022,something_else,"The preparation of the copper based MOF, HKUST-1 [ ... on Vulcan XC-72, dp < 5 nm for Pt, Sigma-Aldrich)."
3582,10.1002/ejoc.200300199,something_else,"Spirane anti-25a: This compound was obtained as a  ... 96, H 8.08, N 3.40; found C 72.76, H 8.24, N 3.26."
3583,10.1002/ejoc.200300199,something_else,"(3S,4S)-3-Dibenzylamino-4-hydroxyhexanoic Acid (sy ... 37, H 7.70, N 4.28; found C 73.25, H 7.84, N 4.16."
3584,10.1002/ejoc.200300199,something_else,"Amino Alcohol syn-23a: This amino alcohol was obta ... 96, H 8.08, N 3.40; found C 72.79, H 8.30, N 3.22."
3585,10.1002/ejoc.200300199,something_else,"Amino Aldehyde 22a: This compound was obtained fro ... 42, H 7.13, N 3.67; found C 72.18, H 7.28, N 3.51."
3586,10.1002/ejoc.200300199,something_else,"Amino Alcohol 21a: Compound 20a (1.15 g, 3.4 mmol) ... 04, H 7.62, N 3.65; found C 72.09, H 7.48, N 3.90."
3587,10.1016/j.apcatb.2014.08.022,something_else,The hydrophobicity level of our samples was determ ... f the amount of benzene adsorbed to that of water.
3588,10.1002/ejoc.200300199,something_else,"Amino Alcohol 20a: A solution of 19a (2.4 g, 5.4 m ... 52, H 6.87, N 4.15; found C 60.32, H 6.89, N 4.12."
3589,10.1002/chem.200903035,something_else,"One-pot synthesis of SSEA-4 hexasaccharide 25. i)  ... 2O 10:8:1:0.7. Troc=2,2,2-trichloroethoxycarbonyl."
3590,10.1016/j.electacta.2012.11.015,something_else,"To a solution of 1 g (5.07 mmol) of 1 dissolved in ... 2.37; N, 8.23. Found: C, 70.67, H, 2.39; N, 8.30%."
3591,10.1002/jhet.2390,something_else,A mixture of 6 2.76 g (0.01 mol) and hydrazonoyl h ... d off and recrystallized from ethanol afforded 14.
3592,10.1002/jhet.2390,something_else,"Equimolar amounts of hydrazine 6 2.76 g (0.01 mol) ... .04. Found: C, 53.74; H, 4.82; N, 19.34; S, 11.00."
3593,10.1002/jhet.2390,something_else,"A solution of compound 8 in ethanol containing sod ... ried, and recrystallized from DMF/EtOH to give 10."
3594,10.1002/jhet.2390,something_else,"To a solution of 3-acetyl-2H-chromen-2-one (1), 3. ... .60. Found: C, 52.12; H, 4.35; N, 20.24; S, 11.64."
3595,10.1002/jhet.2390,something_else,"To a mixture of bishydrazone 3 0.89 g (0.002 mol)  ... l to give the corresponding 4 and 5, respectively."
3596,10.1016/j.tsf.2014.12.015,something_else,We investigated the effect of metal oxide nanopart ... asurement processes were conducted in ambient air.
3597,10.1002/btpr.1988,something_else,Perfusion experiments were carried out by applying ... sign of RFD steps is described by Meier et al.[30]
3598,10.1002/btpr.1988,something_else,Antibodies were further analyzed by a reduced West ... um chloride-5-Bromo-4-chloro-3-indolyl phosphate).
3599,10.1016/j.electacta.2012.11.015,something_else,All reagents and solvents were of reagent grade qu ...  with their 1H NMR spectra and elemental analysis.
3600,10.1002/btpr.1988,something_else,Cell counting of viable cells was conducted three- ... nd 48.88 μm and the aggregation was autocorrected.
3601,10.1002/btpr.1988,something_else,Batch cultures were conducted in a 3 L bioreactor  ... culated with a cell density of 1 x 105 cells mL-1.
3602,10.1002/btpr.1988,something_else,Twice weekly the CHO-DG44 cells were passaged 1:20 ... ally reached cell densities of 1 x 106 cells mL-1.
3603,10.1002/btpr.1988,something_else,Polyethersulfone hollow-fiber membranes were used  ... oreeach experiment removed chemical preservatives.
3604,10.1016/j.sse.2010.03.006,something_else,"Sacrificial Ag electrodes were patterned on a Si w ... surrounded by an oxide shell, as shown in Fig. 11."
3605,10.1016/j.matlet.2008.10.056,something_else,"The Mg-Si binary alloys with three different Si co ... the loss tangent (tanph), which is calculated from"
3606,10.1016/j.electacta.2012.11.015,something_else,Reaction of compound 2 with metal salts (Zn(CH3COO ...  data are consistent with the assigned structures.
3607,10.1016/j.electacta.2012.11.015,something_else,"A mixture of 0.25 g (0.732 mmol) of 4,5-bis(thioph ...  N, 7.79; MS: m/z 1453.47 [M+1]+, 1414.89 [M-Cl]+."
3608,10.1016/j.electacta.2012.11.015,something_else,"A mixture of 0.2 g (0.594 mmol) of 4,5-bis(thiophe ...  C, 67.44; H, 2.32; N, 7.89; MS: m/z 1427.81 [M]+."
3609,10.1002/btpr.1988,something_else,A biocompatibility test[35] was carried out by add ... been sterilized by autoclaving before examination.
3610,10.1002/anie.200800585,something_else,"Synthesis of subunit 7: a) Methacryloyl chloride,  ... sopropylamide, PPTS=pyridinium 4-toluenesulfonate."
3611,10.1002/ejoc.200300199,something_else,"Amino Ester 19a: Compound 18a (3.5 g, 7.9 mmol) wa ... 29, H 6.16, N 3.17; found C 65.48, H 6.26, N 3.02."
3612,10.1002/ejoc.200300199,something_else,"N-Benzyloxycarbonyl-L-aspartic Acid α-Benzyl Ester ... 86, H 5.36, N 3.92; found C 63.77, H 5.24, N 4.09."
3613,10.1002/ejoc.200300199,something_else,"Protected Aminodiol anti-4a: This compound was obt ... 86, H 9.58, N 2.72; found C 69.68, H 9.84, N 2.92."
3614,10.1002/ejoc.200300199,something_else,"Protected Aminodiol syn-4a: A solution of syn-2a ( ... 86, H 9.58, N 2.72; found C 69.74, H 9.78, N 2.80."
3615,10.1002/ejoc.200300199,something_else,"Oxazolidinone cis-3b: Oxazolidinone cis-3b was pre ... , H 10.17, N 4.87; found C 58.26, H 10.36, N 4.69."
3616,10.1002/ejoc.200300199,something_else,"Oxazolidinone trans-3b: Oxazolidinone trans-3b was ... 9, H 10.17, N 4.87; found C 58.32 H 10.38, N 4.75."
3617,10.1002/ejoc.200300199,something_else,"Oxazolidinone cis-3a: This compound was prepared f ... 10, H 9.95, N 5.12; found C 56.92, H 9.78, N 5.24."
3618,10.1002/ejoc.200300199,something_else,"Oxazolidinone trans-3a: A solution of compound syn ... 10, H 9.95, N 5.12; found C 57.18, H 9.69, N 5.32."
3619,10.1002/ejoc.200300199,something_else,"Amino Alcohol anti-2b: Compound anti-2b was obtain ... 41, H 9.81, N 3.17; found C 73.68, H 9.97, N 2.95."
3620,10.1002/ejoc.200300199,something_else,"Amino Alcohol anti-2a: A solution of EtMgBr (8.4 m ... 01, H 9.66, N 3.27; found C 73.23, H 9.86, N 3.09."
3621,10.1002/ejoc.200300199,something_else,"Protected Aminodiol syn-4b: The compound syn-4b wa ... 27, H 9.70, N 2.64; found C 70.47, H 9.88, N 2.38."
3622,10.1002/ejoc.200300199,something_else,"Amino Alcohol syn-2b: Compound syn-2b was obtained ... 1, H 9.81, N 3.17; found C 73.54, H 10.01, N 2.98."
3623,10.1002/ejoc.200300199,something_else,General: The reactions were carried out in oven-dr ... d with a Perkin-Elmer 2400-CHN elemental analyser.
3624,10.1002/ejoc.200300199,something_else,"α-Amino aldehyde derivative 22a reacts with diethy ... d from anti-8a, as described for compound syn-23a."
3625,10.1002/ejoc.200300199,something_else,"Finally, we tested a different protective group of ... lamino aldehyde 22a in very good yield (Scheme 5)."
3626,10.1002/ejoc.200300199,something_else,Alternatively we tested the direct oxidation of am ... on with Ac2O in pyridine at room temp. (Scheme 3).
3627,10.1002/ejoc.200300199,something_else,"Reagents and conditions: (i) MEMCl, DIPEA, CH2Cl2, ... ide, EtOH, reflux. (vi) Ac2O, pyridine, room temp."
3628,10.1016/j.cplett.2010.03.006,something_else,The substrates have been prepared by repeated Ar s ... nsity of the π* resonances with the geometry used.
3629,10.1007/s10853-009-3447-2,something_else,The fibers coated with Ag and Cu were cut to bare  ... ral times to fully get rid of the remained silica.
3630,10.1007/s10853-009-3447-2,something_else,"On the other hand, the coating of copper on the su ... ter bath for 5 h, and the temperature was 50 degC."
3631,10.1002/ejoc.200300199,something_else,"Amino Alcohol syn-2a: A solution of amino aldehyde ... 01, H 9.66, N 3.27; found C 73.11, H 9.82, N 3.12."
3632,10.1002/ejoc.200300199,something_else,"Oxetane 18a: Compound 17a (8.94 g, 25 mmol) was su ... 29, H 6.16, N 3.17; found C 65.55, H 6.34, N 2.97."
3633,10.1002/ejoc.200300199,something_else,"Protected Amino-diol anti-4b: The compound anti-4b ... 27, H 9.70, N 2.64; found C 70.38, H 9.90, N 2.44."
3634,10.1002/ejoc.200300199,something_else,"Amino Alcohol anti-5a: The amino alcohol anti-5a w ... 79, H 8.79, N 3.49; found C 71.70, H 8.62, N 3.63."
3635,10.1002/ejoc.200300199,something_else,"Methyl (S)-3-Dibenzylamino-4-(tert-butyldimethylsi ... 21, H 8.72, N 3.28; found C 70.07, H 8.75, N 3.32."
3636,10.1002/ejoc.200300199,something_else,"Methyl (S)-3-[(Benzyloxycarbonyl)amino]-4-(tert-bu ... 81, H 8.19, N 3.67; found C 59.92, H 8.28, N 3.47."
3637,10.1002/ejoc.200300199,something_else,"(S)-3-Dibenzylaminobutyrolactone (14a): This compo ... 84, H 6.81, N 4.98; found C 76.93, H 6.83, N 4.93."
3638,10.1002/ejoc.200300199,something_else,"Methyl (S)-3-[(Benzyloxycarbonyl)amino]-4-hydroxyb ... 42, H 6.41, N 5.24; found C 58.45, H 6.42, N 5.20."
3639,10.1002/ejoc.200300199,something_else,"(S)-2-[(Benzyloxycarbonyl)amino]-3-(methoxycarbony ... 51, H 5.38, N 4.98; found C 55.83, H 5.42, N 4.96."
3640,10.1002/ejoc.200300199,something_else,Methyl (S)-3-Dibenzylamino-4-hydroxybutanoate (11a ... tonized completely after 12 h in the refrigerator.
3641,10.1002/ejoc.200300199,something_else,"(3S,4R)-3-Amino-4-hydroxyhexanoic Acid (anti-8a):  ... 97, H 8.90, N 9.52; found C 48.04, H 8.80, N 9.58."
3642,10.1002/ejoc.200300199,something_else,"(3S,4S)-3-Amino-4-hydroxyhexanoic Acid (syn-8a): 2 ... 97, H 8.90, N 9.52; found C 49.07, H 8.87, N 9.73."
3643,10.1002/ejoc.200300199,something_else,"Amino Alcohol syn-5a: A solution of syn-4a (1.14 g ... 79, H 8.79, N 3.49; found C 71.51, H 8.67, N 3.71."
3644,10.1002/ejoc.200300199,something_else,"Amino Acid anti-7b: The compound anti-7b was obtai ... 00, H 8.94, N 4.01; found C 54.88, H 8.97, N 3.96."
3645,10.1002/ejoc.200300199,something_else,"Amino Acid anti-7a: The protected amino acid anti- ... 72, H 8.72, N 4.18; found C 53.81, H 8.75, N 4.11."
3646,10.1002/ejoc.200300199,something_else,"Amino Acid syn-7a: A solution of syn-6a (289 mg, 0 ... 72, H 8.72, N 4.18; found C 53.76, H 8.77, N 4.14."
3647,10.1002/ejoc.200300199,something_else,"Amino Alcohol anti-6b: The amino alcohol anti-6b w ... 9, H 9.92, N 4.18; found C 57.11, H 10.12, N 4.00."
3648,10.1002/ejoc.200300199,something_else,"Amino Alcohol syn-6b: The amino alcohol syn-6b was ... 9, H 9.92, N 4.18; found C 57.08, H 10.06, N 4.02."
3649,10.1002/ejoc.200300199,something_else,"Amino Alcohol anti-6a: The compound anti-6a was ob ... 05, H 9.72, N 4.36; found C 55.75, H 9.69, N 4.21."
3650,10.1002/ejoc.200300199,something_else,"Amino Alcohol syn-6a: A solution of dibenzylamino  ... 05, H 9.72, N 4.36; found C 55.80, H 9.75, N 4.30."
3651,10.1002/ejoc.200300199,something_else,"Amino Alcohol anti-5b: The amino alcohol anti-5b w ... 26, H 8.97, N 3.37; found C 72.16, H 8.90, N 3.31."
3652,10.1002/ejoc.200300199,something_else,"Amino Alcohol syn-5b: The amino alcohol syn-5b was ... 26, H 8.97, N 3.37; found C 72.52, H 9.15, N 3.12."
3653,10.1002/ejoc.200300199,something_else,"Amino Acid syn-7b: The compound syn-7b was obtaine ... 00, H 8.94, N 4.01; found C 54.83, H 9.15, N 3.90."
3654,10.1002/anie.200800585,something_else,We then focused our efforts on the synthesis of th ...  equiv) in THF18 to afford the targeted subunit 7.
3655,10.1002/anie.200800585,something_else,"Synthesis of subunit 6 a: a) LiAlH4, Et2O, 99 %; b ... methylaminopyridine, HMPA=hexamethylphosphoramide."
3656,10.1002/app.34559,something_else,"The HIPS/SBS/CB antistatic sheets were prepared by ... abender, Germany) to obtain the antistatic sheets."
3657,10.1016/j.jallcom.2005.10.011,something_else,"Sodium tungstate, Na8WO3 was prepared by grinding  ... e checked the literature, this is a new tungstate."
3658,10.1016/j.actamat.2010.10.058,something_else,The rectangular specimens used to measure Young's  ... and the results are within 1% of published values.
3659,10.1016/j.actamat.2010.10.058,something_else,Neutron powder diffraction was used to measure the ... d Cu feedstock powders and corresponding coatings.
3660,10.1016/j.actamat.2010.10.058,something_else,All coatings were sprayed using a temperature opti ... or to being accelerated through the nozzle throat.
3661,10.1016/j.actamat.2010.10.058,something_else,The substrate materials used were electrical grade ... using 1200 grit SiC paper and rinsed with ethanol.
3662,10.1016/j.jssc.2014.03.010,something_else,"Recycling tests for Knoevenagel reaction over 46-A ... te (1.0 mmol), catalyst (0.05 g), 20 min, 80 degC."
3663,10.1016/j.jssc.2014.03.010,something_else,Recycling experiments were carried out for the eva ... ention of high catalytic activity and selectivity.
3664,10.1016/j.jssc.2014.03.010,something_else,"The catalyst (0.05 g), benzene (3 mL), benzaldehyd ...  with an OV-101 capillary column and FID detector."
3665,10.1016/j.jorganchem.2006.10.015,something_else,Reactions were carried out by using standard Schle ... e University of Kentucky Mass Spectrometry Center.
3666,10.1016/j.jssc.2014.03.010,something_else,The amino-Al-containing mesoporous KIT-6 and the a ...  grafted onto the surface of KIT-6 and x-Al-KIT-6.
3667,10.1016/j.nanoen.2014.12.041,something_else,To make the slurry of adhesive and conductive Sn a ... lectrolyte of 75 ul was applied for one coin cell.
3668,10.1016/j.nanoen.2014.12.041,something_else,"Both-types of spherical Sn particles, with nano- ( ... ions of synthesized Sn particles are in Figure S1."
3669,10.1016/j.jnoncrysol.2007.11.012,something_else,"Four compositions were chosen, with 30 and 10 wt%  ... mpositions were measured by SEM-EDX analysis [22]."
3670,10.1016/j.cattod.2011.11.015,something_else,"The morphological characterization of modified HOP ... 0 kHz (TESP, Veeco), at a scan rate of 1.0-1.5 Hz."
3671,10.1016/j.cattod.2011.11.015,something_else,The activated graphite electrodes (HOPGET) were mo ... lipore-Q water and kept under N2 till further use.
3672,10.1016/j.cattod.2011.11.015,something_else,"The chemicals and solvents were analytical grade,  ... measurements were carried out at room temperature."
3673,10.1016/j.jcat.2003.11.008,something_else,"The cis- and tr-4-TBCHL selectivities over catalys ... 700 degC, in the reactor at 500 degC) at 100 degC."
3674,10.1016/j.jcat.2003.11.008,something_else,"Amount of cis- and tr-4-TBCHL produced as a functi ... 700 degC, in the reactor at 500 degC) at 100 degC."
3675,10.1016/j.nanoen.2014.12.041,something_else,For material characterization during and after ele ...  morphology of materials (Supporting Information).
3676,10.1016/j.jcat.2003.11.008,something_else,DRIFT Spectra in the OH-stretching region of catal ...  in the reactor at 500 degC) recorded at 100 degC.
3677,10.1016/j.jorganchem.2006.10.015,something_else,"In a 25-mL round-bottom flask, ferrocenecarboxalde ... 9 (t, 2H, 3J = 2.0 Hz, C4H5), 8.10 (br s, 1H, CH)."
3678,10.1016/j.jorganchem.2006.10.015,something_else,"In a 125-mL Schlenk flask, 3 (370 mg, 1.61 mmol) a ... 6.25; N, 5.99. Found: C, 60.94; H, 6.15; N, 6.00%."
3679,10.1016/j.jelechem.2008.08.001,something_else,The preparation of the bis(alkylthio)-substituted  ... nal step of the synthesis is outlined in Scheme 1.
3680,10.1002/jssc.201400635,something_else,A calibration curve was prepared by serially dilut ... g/mL with correlation coefficients (r2) of 0.9993.
3681,10.1002/jssc.201400635,something_else,The use of vortex in the VSLME procedure can incre ... rpm and left soaking for a further 30 min is used.
3682,10.1002/jssc.201400635,something_else,The AAC was prepared in-house. The binding buffer  ... roxide solution (2 M) and hydrochloric acid (2 M).
3683,10.1002/jssc.201400635,something_else,"A standard solution of OTA (1.0 mg/mL in methanol) ... ch-Science Tool Master S system (Shanghai, China)."
3684,10.1016/j.jmatprotec.2007.03.032,something_else,Electro-discharge diamond grinding (EDDG) is a hyb ... electrically conducting hard-to-machine materials.
3685,10.1007/s11051-012-1089-9,something_else,In order to characterize the nanoparticles by X-ra ... range 2θ = 4-50deg with a speed counting 1deg/min.
3686,10.1007/s11051-012-1089-9,something_else,"The ""as prepared"" bimetallic catalysts were charac ... the colloids or precipitate was dissolved in HNO3."
3687,10.1016/j.jorganchem.2006.10.015,something_else,"In a 50-mL Schlenk flask, 2 (480 mg, 2.11 mmol) wa ... , 2H, C4H5), 4.10 (s, 5H, Cp), 4.16 (m, 2H, C4H5)."
3688,10.1002/adma.201401372,something_else,"For PEG modification, 500 μL of 69Ge-SPION@PAA in  ... nd re-dispersed in PBS before injection into mice."
3689,10.1002/adma.201401372,something_else,"Germanium-69 was produced by 69Ga(p,n)69Ge reactio ... lidic purity of 69Ge was determined to be >99.99%."
3690,10.1016/j.surfcoat.2013.06.072,something_else,Samples to be subjected to microstructural investi ...  using diamond paste down to 0.5 μm particle size.
3691,10.1016/j.surfcoat.2013.06.072,something_else,Some samples were subjected to a subsequent anneal ... d hence not requiring any further annealing steps.
3692,10.1016/j.jorganchem.2006.10.015,something_else,Di(N-(ferrocenylmethyl))-N-methylamine (5) was obt ... ctroscopically and by using X-ray crystallography.
3693,10.1016/j.jorganchem.2006.10.015,something_else,Myer and Allen reported the synthesis of N-(ferroc ...  so obtained is pure enough for further reactions.
3694,10.1016/j.jorganchem.2006.10.015,something_else,Reaction of ferrocenecarboxaldehyde (1) [29] with  ... or 18 h. The reactions are summarized in Scheme 3.
3695,10.1016/j.jorganchem.2006.10.015,something_else,"In a 125-mL Schlenk flask, 4 (80.0 mg, 0.171 mmol) ... 5.84; N, 6.01. Found: C, 62.26; H, 5.99; N, 5.39%."
3696,10.1016/j.jorganchem.2006.10.015,something_else,"Di(N-(ferrocenylmethyl))-N-methylamine was synthes ... 5.90; N, 3.28. Found: C, 64.44; H, 5.87, N, 3.36%."
3697,10.1002/adma.201401372,something_else,"Synthesis of 69Ge-SPION@PEG: In order to label SPI ... g through a PD-10 column, preconditioned with PBS."
3698,10.1016/j.jelechem.2008.08.001,something_else,Voltammetric measurements were carried out with an ... lectrode (CME) for studies in the condensed state.
3699,10.1016/j.jcat.2003.11.008,something_else,"For the analysis of the OH-stretching region (4000 ...  temperature under nitrogen flow (33 ml/min, STP)."
3700,10.1016/j.jcat.2003.11.008,something_else,Three different catalyst samples were prepared fro ... linity (XRD) or in the particle-size distribution.
3701,10.1016/j.optmat.2011.11.008,something_else,"Concentration dependences of hemolysis induced by  ... /mL, 6 was black control, 7 was positive control)."
3702,10.1016/j.optmat.2011.11.008,something_else,The as-synthesized PbSe QDs with different concent ... centrations on hemolysis rate can be seen clearly.
3703,10.1016/j.optmat.2011.11.008,something_else,A weight 3 kg rabbit was provided by the Animal Ex ...  The hemolytic rate was calculated as follow [28]:
3704,10.1016/j.optmat.2011.11.008,something_else,0.1 mmol of lead acetate trihydrate was dissolved  ...  The precipitate of QDs was re-dispersed in water.
3705,10.1016/j.optmat.2011.11.008,something_else,"Briefly, 10 mL of deionic water was added into a 1 ... rature under the protection of N2 for further use."
3706,10.1016/j.optmat.2011.11.008,something_else,"DHLA was prepared according to literatures [27], [ ... on of the synthesis process of dihydrolipoic acid."
3707,10.1016/j.optmat.2011.11.008,something_else,"Lipoic acid (LA) (95+%) was obtained from Fluka, l ... ents was deionized to a resistively of 18.2 MΩ cm."
3708,10.1016/j.tetlet.2010.03.018,something_else,"Next, to show the useful extension of this spartei ... followed by mono-defluorination via β-elimination."
3709,10.1016/j.jeurceramsoc.2010.12.001,something_else,The corrosion experiments were conducted in 50 or  ...  The exposure time varied between 168.5 and 264 h.
3710,10.1016/j.fuel.2005.03.008,something_else,"In this work, two typical Chinese petroleum cokes, ... each activation process has been given in Table 3."
3711,10.1016/j.energy.2006.04.007,something_else,"System no. 1 is selected as the reference case bec ... e tank, which has electricity as a back-up source."
3712,10.1016/j.esd.2010.06.002,something_else,The hood systems work by collecting all of the exh ... pollutant emitted per test phase is then reported.
3713,10.1016/j.esd.2010.06.002,something_else,The wood stoves were tested using kiln-dried Dougl ... dies on stove performance using these other fuels.
3714,10.1016/j.sse.2010.03.005,something_else,A thin film of La2O3 with a thickness ranging from ... ited as a bottom electrode by thermal evaporation.
3715,10.1016/j.jmatprotec.2006.03.152,something_else,Predetermined quantities of the molten alloys were ... es of the alloys of interest are shown in Table 3.
3716,10.1016/j.jmatprotec.2006.03.152,something_else,In order to obtain three hyper eutectic Pb-Sn allo ... primary phase content present in a specific alloy.
3717,10.1016/j.ces.2011.05.015,something_else,"Flow regimes observed for liquid-liquid systems in ... ssion. Copyright American Chemical Society, 2011.)"
3718,10.1016/j.ces.2011.05.015,something_else,"As discussed above, the conventional offline analy ... s investigating kinetics and transport parameters."
3719,10.1016/j.energy.2006.04.007,something_else,"Systems no. 4-6 are similar to the first system, t ... ave, in addition, a mechanical ventilation system."
3720,10.1016/j.jcat.2003.11.008,something_else,"The MPV reactions were carried out in a vertical,  ...  that no internal mass transfer limitations exist."
3721,10.1016/j.jeurceramsoc.2010.12.001,something_else,Before and after the corrosion experiments the cer ... ed into H2SO4 without intermittent weighing steps.
3722,10.1016/j.elecom.2009.08.042,something_else,The nanoporous AAO membranes which are 60 μm thick ... a standard three-electrode electrochemical system.
3723,10.1016/j.surfcoat.2004.12.005,something_else,"After the deposition of the coatings, the specimen ... vestigated by electron probe microanalysis (EPMA)."
3724,10.1016/j.cplett.2010.03.009,something_else,Ti foils (99.6% purity) were anodized in ethylene  ...  area (10 cm2) and a thickness of about 5 μm [23].
3725,10.1016/j.cplett.2010.03.034,something_else,The anhydrous samples of 1-butanol of purity 99.8% ... lasted over 1 h to be sure the sample solidified).
3726,10.1016/j.solmat.2006.07.005,something_else,SnCl2Pc and pentacene (Pn) powders were purified b ... as 180 and 800 nm. The deposition rate was 1 nm/s.
3727,10.1007/s10008-010-1049-1,something_else,Fast spectroscopic studies in the spectral range 3 ... per are presented vs. Ag/AgCl reference electrode.
3728,10.1007/s10008-010-1049-1,something_else,"PAMPSA (Aldrich, MW 2,000,000, 15% aqueous solutio ...  of unreacted aniline, APS, and other by-products."
3729,10.1016/j.electacta.2012.11.012,something_else,Electrochemical studies were performed using a cyc ...  the normalization parameters of the measurements.
3730,10.1016/j.electacta.2012.11.012,something_else,"For the swelling degree analyses, all hydro-sponge ...  was established. Eq. (2) was used to calculate Q:"
3731,10.1016/j.jeurceramsoc.2010.12.001,something_else,To determine and quantify the dissolution of yttri ... asure of mass loss per surface area unit (μg/cm2).
3732,10.1016/j.electacta.2012.11.012,something_else,All hydro-sponges were filtered by vacuum suction  ...  were processed using the ImageJ software package.
3733,10.1016/j.electacta.2012.11.012,something_else,"For the synthesis of hydro-sponge III, the pH of 2 ... aterial was immersed in 1 mol L-1 NaOH for 3 days."
3734,10.1016/j.electacta.2012.11.012,something_else,"For hydro-sponge II, the synthesis was the same as ... system before the addition of the pyrrole monomer."
3735,10.1016/j.electacta.2012.11.012,something_else,"Four different hydro-sponges, numbered I to IV, we ... rred for 1 min and then left undisturbed for 24 h."
3736,10.1016/j.electacta.2012.11.012,something_else,"Pyrrole, ammonium peroxysulfate (APS) and β-cyclod ... d before use, all materials were used as received."
3737,10.1016/j.electacta.2008.02.085,something_else,Cobalt is present in trace amounts in virtually al ... overy revealed the utility of the proposed sensor.
3738,10.1016/j.electacta.2008.02.085,something_else,To assess the practical applicability of the senso ... ensor for determination of cobalt in real samples.
3739,10.1016/j.electacta.2008.02.085,something_else,The PVC-based membranes were prepared by dissolvin ... re equilibrated for 2 days in 0.1 M Co2+ solution.
3740,10.1016/j.elecom.2009.08.042,something_else,"The gold nanowires were electrodeposited from the  ... for two times, exposing the top of gold nanowires."
3741,10.1016/j.electacta.2012.11.012,something_else,"Hydro-sponge IV was synthesized by the addition of ... d for comparison with hydro-sponges I, II and III."
3742,10.1002/jhet.2390,something_else,"A mixture of 6 2.76 g (0.01 mol) and hydrazonoyl h ... ed the corresponding 15, 16, and 17, respectively."
3743,10.1016/j.jelechem.2008.08.001,something_else,"The CME [16] and [17], provided by the ""French Cav ... vent; no pre-treatment of the electrode is needed."
3744,10.1016/j.jelechem.2008.08.001,something_else,C2 is a waxy material. It is easily deposited on t ... ted in condensed state onto the working electrode.
3745,10.1016/j.msea.2015.04.004,something_else,An extruded 10 mm rod of AZ91 magnesium alloy (Mg- ... ting and the resultant percentages of elongations.
3746,10.1016/j.matdes.2015.09.116,something_else,The etched liquid was the modified Kroll's reagent ... ohol and 5% perchloric acid at 15 V and - 35 degC.
3747,10.1016/j.matdes.2015.09.116,something_else,"Master ingot with the nominal composition of Ti44A ... 1.67 μm/s, 16.67 μm/s and 21.67 μm/s respectively."
3748,10.1016/j.brainres.2004.11.030,something_else,"GHB (sodium salt; Laboratorio Farmaceutico C.T., S ... ml/kg). All drugs were injected intraperitoneally."
3749,10.1016/j.brainres.2004.11.030,something_else,"One hour after the first trial, independent groups ...  beginning of the acceleration phase was recorded."
3750,10.1016/j.tetlet.2014.06.069,something_else,"Although syntheses and studies of some fluorinated ... trimerization at lower temperatures. 23, 24 and 25"
3751,10.1002/smll.200800279,something_else,"Coaxial nanofibers were electrospun using 15-17 wt ... etailed overview of the experimental set up.16, 17"
3752,10.1002/smll.200800279,something_else,"Polystyrene-b-polyisoprene denoted as SI(54-70), w ... nally selective towards the PI phase of the BCP.15"
3753,10.1016/j.jpcs.2014.04.012,something_else,"Filled skutterudite Ce0.8Fe3CoSb12.1 ingots were p ... , as reported in high pressure x-ray studies [14]."
3754,10.1016/j.scriptamat.2006.05.037,something_else,Alloy of Ti40Zr29Cu9Ni8Be14 composition was prepar ... old having cylindrical cavity of 1 mm in diameter.
3755,10.1016/j.ica.2009.01.001,something_else,The nonlinear measurements were performed in solid ... kness was measured by using a Dektak 6 M profiler.
3756,10.1016/j.ica.2009.01.001,something_else,"Solution of NaOH (6.0 ml, 10%) was added portionwi ... 1,4-diene-3-ones 5a-e, yield 2.43-3.60 g (71-80%)."
3757,10.1016/j.ica.2009.01.001,something_else,"A mixture of FcCHO (4.3 g, 0.02 mol), acetylaceton ... ; Fe, 18.86. Found: S, 64.71; H, 5.69; Fe, 18.74%."
3758,10.1016/j.ica.2009.01.001,something_else,"The 1H and 13C NMR spectra were recorded on a Unit ... yclic voltammetry, was 0.660 V vs. Ag/AgCl (DMSO)."
3759,10.1007/s10854-006-9034-2,something_else,"The deposition of a typical Cd0.5Zn0.5Se thin film ... lled water, dried in air and kept in a dessicator."
3760,10.1007/s10854-006-9034-2,something_else,Substrate cleaning plays an important role in the  ... ble distilled water before deposition of the film.
3761,10.1016/j.matlet.2008.10.057,something_else,"A transmission electron microscope (TEM) (Philips, ... izer nano ZS) was used to measure zeta potentials."
3762,10.1016/j.matlet.2008.10.057,something_else,All chemicals were purchased from Aldrich and used ... ed. The remaining nanoparticles were dried in air.
3763,10.1016/j.ica.2009.01.001,something_else,"3-Ferrocenylmethylidenepentane-2,4-dione (4) was f ... re and purified by recrystallization from ethanol."
3764,10.1002/pola.27188,something_else,The self-polycondensation of the AB monomer was pe ...  weight distribution (Mw/Mn) in the range 1.2-1.6.
3765,10.1016/j.jallcom.2007.10.075,something_else,All chemical reagents are analytical grade. H2PtCl ... with 5 M HNO3 for 24 h under refluxing conditions.
3766,10.1016/j.jallcom.2007.10.075,something_else,Nitrogen adsorption-desorption isotherms were obta ... rformed by using the XPSPEAK Version 4.1 software.
3767,10.1002/app.34559,something_else,"Commercial grade of HIPS (HI 410T) with 7.5 g/10 m ... 2) (Cabot Co., Boston, MA) was used in this study."
3768,10.1016/j.jelechem.2014.11.032,something_else,We used TGA to measure the content of Pt in the Pt ...  very high during Pt@MWNT nanocomposite synthesis.
3769,10.1016/j.jelechem.2014.11.032,something_else,"Glassy carbon electrode (GCE, 3 mm in diameter) wa ... working electrode for all electrochemical studies."
3770,10.1016/j.jelechem.2014.11.032,something_else,10.0 mg of MWNTs were dispersed in 20.0 mL triethy ...  dried under reduced pressure at 60 degC for 15 h.
3771,10.1016/j.jelechem.2014.11.032,something_else,"MWNTs of >95% purity, 20-40 nm diameter, and 5-15  ... 2SO4, and other reagents were of analytical grade."
3772,10.1002/syn.20902,something_else,Rats were designated to receive a single injection ... ps (P < 0.05). Data are expressed as means +- SEM.
3773,10.1002/syn.20902,something_else,"Beginning at PND 40, rats received 2 biweekly inje ... led until their core temperature reached 39.5degC."
3774,10.1002/adfm.201102968,something_else,"Device Fabrication: Inverted polymer solar cells w ... K, Hamamatsu, Japan) were used to measure the EQE."
3775,10.1016/j.jallcom.2007.10.075,something_else,"For the production of binary supported catalyst, V ...  all catalysts in this study were fixed at 20 wt%."
3776,10.1002/adfm.201102968,something_else,Film Preparation and Characterization: The deposit ...  for comparison with Al2O3:ZnO nanolaminate films.
3777,10.1016/j.aca.2015.09.044,something_else,"The lysis of the bacteria and the DNA extraction a ... (Nanodrop2000spectophotometer, Thermo Scientific)."
3778,10.1016/j.aca.2015.09.044,something_else,"The Expand High Fidelity PCR System Kit (Roche Mol ... ol L-1 sodium phosphate, 0.1 mol L-1 KCl, pH 7.0)."
3779,10.1016/j.ces.2008.03.003,something_else,"Protein bands on the SDS-PAGE gel were transferred ... phate Conjugate Substrate Kit, 170-6432, Bio-Rad)."
3780,10.1016/j.ces.2008.03.003,something_else,IBs (mainly gloshedobin with or without the trunca ... ta was processed with LP Data View V1.03 software.
3781,10.1016/j.ces.2008.03.003,something_else,E. coli BL21(DE3) cells (Novagen) were transformed ... LE was conducted using the same protocol as above.
3782,10.1016/j.jallcom.2007.10.075,something_else,"Firstly, the MEAs were activated at 80 degC for 24 ... em (Arbin Instr. Corp.) at constant current model."
3783,10.1016/j.jallcom.2007.10.075,something_else,Commercial Nafion 117 membranes (DuPont) were used ... for 3 min. The active area of the MEA is 4.41 cm2.
3784,10.1016/j.jallcom.2007.10.075,something_else,"For the electrochemical evaluation, all potentials ... 18 to 1 V at a scan rate 50 mV s-1 under nitrogen."
3785,10.1016/j.aca.2015.09.044,something_else,"For the immobilization of the single-tagged amplic ... erica, L. monocytogenes and E. coli, respectively."
3786,10.1016/j.jelechem.2008.08.001,something_else,"The supporting electrolyte, (n-Bu4N)[PF6] (Fluka,  ... as polished with a polishing machine (Presi P230)."
3787,10.1002/pola.27188,something_else,Scheme 1 shows the strategy for the synthesis of l ... the self-polycondensation of the AB2 macromonomer.
3788,10.1002/pola.27188,something_else,In a three-necked flask equipped with a Dean-Stark ... d in vacuo at 100 degC for 5 h. The yield was 96%.
3789,10.1002/bit.24438,something_else,"FT-IR of GOx (A), PQQ (B), and MWCNTs-GOx-PQQ kept ... e, available at http://wileyonlinelibrary.com/bit]"
3790,10.1002/bit.24438,something_else,"Recent studies in the field of MWCNTs modified ele ... ht, adsorption of GOx and PQQ occur on the MWCNTs."
3791,10.1002/bit.24438,something_else,"Afterwards, 3 uL of pyrrole were added to each sus ... ltrapure water and stored in the fridge until use."
3792,10.1002/bit.24438,something_else,"Next day, the suspensions were hydrodynamically st ... cy and 160 Vp-p amplitude was applied for few min."
3793,10.1002/bit.24438,something_else,Glassy carbon (GC) disk electrodes (1 mm in diamet ...  the bioanode and biocathode is shown in Figure 1.
3794,10.1002/bit.24438,something_else,Ultrapure water milliQ grade with resistivity of 1 ... glucose in serum H4522 was determined to be ~5 mM.
3795,10.1016/j.bbrc.2003.12.166,something_else,"Effects of amthamine, PGE2, and forskolin on U-937 ...  +- SEM of triplicate assays. *p<0.01 vs. control."
3796,10.1016/j.bbrc.2003.12.166,something_else,"Desensitization of PGE2r and H2r induced by forsko ... d cells stimulated with PGE2 and H2, respectively."
3797,10.1002/bit.24438,something_else,"The stability of the prepared MWCNTs based BFC was ... zyme, mediators or MWCNTs from the deposited film."
3798,10.1016/j.bbrc.2003.12.166,something_else,Desensitization of PGE2- and amthamine-induced cAM ... 05 vs. PGE2 pretreated cells stimulated with PGE2.
3799,10.1016/j.bbrc.2003.12.166,something_else,Intracellular Ca2+Measurements. Fura 2-AM was used ... s calculated according to Grynkiewicz et al. [17].
3800,10.1016/j.bbrc.2003.12.166,something_else,"Western blots. Cells were lysed in sample buffer ( ... instructions (Amersham, Buckinghamshire, England)."
3801,10.1016/j.bbrc.2003.12.166,something_else,Proliferation assay. The MTT test was performed as ...  vertical ELISA Titertek Multiscan MCC/340 reader.
3802,10.1016/j.bbrc.2003.12.166,something_else,"For time-course cAMP accumulation studies, cells w ...  the specific agents at different periods of time."
3803,10.1016/j.bbrc.2003.12.166,something_else,"For desensitization assays, pretreatment of cells  ... hether the system was still able to generate cAMP."
3804,10.1016/j.bbrc.2003.12.166,something_else,Cell culture. U-937 cells were cultured at 37 degC ... with 10% fetal calf serum and 50 μg/ml gentamicin.
3805,10.1016/j.bbrc.2003.12.166,something_else,"Materials. Cell culture medium, isobutylmethylxant ... All other chemicals used were of analytical grade."
3806,10.1016/j.vacuum.2010.02.011,something_else,The working electrodes were prepared by mixing act ... ed at frequency range between 100 kHz and 0.01 Hz.
3807,10.1016/j.bbrc.2003.12.166,something_else,Concentration-response curves to cAMP production.  ... btained in at least three independent experiments.
3808,10.1002/pola.27188,something_else,1H and 13C NMR spectra were recorded using a JEOL  ...  the measurements was checked by time sweep tests.
3809,10.1016/j.applthermaleng.2005.09.021,something_else,A pressure transducer connected to the test sectio ... stem temperatures were steady for at least 10 min.
3810,10.1016/j.jallcom.2013.04.063,something_else,Photocatalytic degradation studies were performed  ... ter reaction and C0 was the initial concentration.
3811,10.1002/pola.27188,something_else,"In a round-bottom flask, the AB2 macromonomer prec ...  in vacuo at 100 degC for 10 h. The yield was 98%."
3812,10.1002/pola.27188,something_else,In a three-necked flask equipped with a Dean-Stark ...  vacuo at 100 degC for 10 h. The yield was 4.91 g.
3813,10.1002/pola.27188,something_else,"An AB monomer, 4-chloro-4'-(4-hydroxyphenyloxy)dip ... urchased from Kanto Chemical and used as received."
3814,10.1016/j.jcat.2004.09.009,something_else,Temperature-programmed desorption (TPD) of ammonia ... oward ammonia was done just after each experiment.
3815,10.1016/j.jcat.2004.09.009,something_else,Calcination of group 13 element-containing silsesq ... d at 823 K in the same manner just before the use.
3816,10.1016/j.jcat.2004.09.009,something_else,"To a hexane solution (70 cm3) of (t-C4H9O)3SiOH (2 ... 9.67; N, 1.56%. Found C, 54.29; H, 9.55; N, 1.52%."
3817,10.1016/j.jcat.2004.09.009,something_else,"A similar method for 3d was adopted by using (i-C4 ... 8.02; N, 0.74%. Found C, 43.62; H, 7.61; N, 0.69%."
3818,10.1016/j.jcat.2004.09.009,something_else,"A similar method for 2b-h was adopted by using (c- ... 7.27; N, 0.73%. Found C, 48.37; H, 6.96; N, 0.62%."
3819,10.1016/j.applthermaleng.2005.09.021,something_else,Bubble dynamic parameters and pool boiling heat tr ... n plasma coated tubes in saturated R134a and R600a
3820,10.1016/j.jcat.2004.09.009,something_else,All synthetic procedures were carried out under an ... corresponding ammonium cations in moderate yields.
3821,10.1016/j.tsf.2014.12.018,something_else,"A commercially pure titanium (ASTM grade 2) plate, ... de at the voltages of 200 and 300 V, respectively."
3822,10.1016/j.cattod.2011.11.012,something_else,The NO + O2 adsorption test was carried out in the ... ransform Infrared (FTIR) analyzer described above.
3823,10.1016/j.cattod.2011.11.012,something_else,The catalysts (0.4 in. length with 0.75 in. diamet ... tions of NO and NO2 reported by the FTIR analyzer.
3824,10.1016/j.cattod.2011.11.012,something_else,Hydrogen temperature programmed reduction (H2-TPR) ... itrogen jar before the gases went through the TCD.
3825,10.1016/j.cattod.2011.11.012,something_else,"4%Pd/Al2O3(Sasol), 2%Rh/CeO2-ZrO2 (Rhodia) and 20% ... overnight and calcined at 550 degC for 5 h in air."
3826,10.1016/j.msea.2015.07.043,something_else,"Twenty-five kilograms ingot of a Fe-Mn-Al-C steel  ... re 1060 degC, 870 degC and 250 degC, respectively."
3827,10.1016/j.chemphys.2015.09.006,something_else,Experiments were carried out at 298 K using a Vari ... ls were then left at room temperature to solidify.
3828,10.1016/j.jallcom.2013.04.063,something_else,Typical FESEM images of the products synthesized a ... . (a and b) 2 mL; (c and d) 5 mL; (e and f) 38 mL.
3829,10.1016/j.jcat.2004.09.009,something_else,"Trimethylaluminum in hexane solution (1 M), (c-C5H ... an and Shokubai Kasei Kogyo Co.Ltd., respectively."
3830,10.1002/jhet.2390,something_else,"A suspension of 6 2.76 g (0.01 mol) and excess of  ... .54. Found: C, 51.35; H, 3.93; N, 18.45; S, 10.50."
3831,10.1002/jhet.2390,something_else,"A mixture of 6 2.76 g (0.01 mol) and tetrabromophe ... d: C, 33.23; H, 1.44; Br, 44.31; N, 7.72; S, 4.40."
3832,10.1002/jhet.2390,something_else,"To a stirred solution of 6 2.76 g (0.01 mol) in hy ... .16. Found: C, 50.21; H, 3.20; N, 24.42; S, 11.12."
3833,10.1016/j.actbio.2013.03.019,something_else,"For subcutaneous injections, one of the bilateral  ...  stained samples were corrected for white balance."
3834,10.1016/j.actbio.2013.03.019,something_else,"For subcutaneous injection, 25 μl of blood was dra ... ime point of non-injected and HA-injected samples."
3835,10.1016/j.actbio.2013.03.019,something_else,"Before injection, animals were anesthetized with 5 ... 3 rats per condition were required per experiment."
3836,10.1016/j.actbio.2013.03.019,something_else,"For intramyocardial injection, the pre-gelation ti ... dramatically reduced or the crosslinker is absent."
3837,10.1016/j.actbio.2013.03.019,something_else,All animals received humane care in compliance wit ... force microscopy (AFM)) and histological analysis.
3838,10.1016/j.actbio.2013.03.019,something_else,"Thiolated hyaluronic acid was obtained directly fr ... A/0.9% PEGDA hydrogel, unless otherwise indicated."
3839,10.1016/j.polymer.2010.12.052,something_else,"Fluorescence spectra of CS-g-PCL(-g-P(MEO2MA-co-OE ... nd 46 degC, respectively (concentration: 1 mg/mL)."
3840,10.1016/j.polymer.2010.12.052,something_else,Plots of transmittance as a function of temperatur ... elle solution (sample 2) (concentration: 2 mg/mL).
3841,10.1016/j.actbio.2013.03.019,something_else,Remaining slides from subcutaneous and intramyocar ... nd host tissue positions for fluorescence imaging.
3842,10.1016/j.polymer.2010.12.052,something_else,P(MEO2MA-co-OEGMA)-N3 was prepared by two steps. P ... of azide absorbance peak in P(MEO2MA-co-OEGMA)-N3.
3843,10.1016/j.polymer.2010.12.052,something_else,Doxorubicin hydrochloride (2 mg) was stirred with  ... y in PBS solution was 2 mg. The EE% is defined as:
3844,10.1016/j.polymer.2010.12.052,something_else,"Samples for transmittance, TEM, DLS, and fluoresce ... mg/mL for TEM, DLS, and fluorescence measurements."
3845,10.1016/j.polymer.2010.12.052,something_else,Amphiphilic CS graft copolymers were prepared via  ... roduct was obtained by precipitated from n-hexane.
3846,10.1016/j.polymer.2010.12.052,something_else,P(MEO2MA-co-OEGMA)-N3 was prepared by two steps. F ... ne. The obtained product was then dried in vacuum.
3847,10.1016/j.polymer.2010.12.052,something_else,Pyrene-PCL-N3 was synthesized by three steps. Firs ... ne. The obtained product was then dried in vacuum.
3848,10.1016/j.polymer.2010.12.052,something_else,CS was heated with excess phthalic anhydride (PA)  ... fied solid product was dried in vacuum at 40 degC.
3849,10.1016/j.polymer.2010.12.052,something_else,ATR FT-IR spectra of the samples were recorded on  ...  recorded with an excitation wavelength at 320 nm.
3850,10.1016/j.polymer.2010.12.052,something_else,"CS (viscosity = 200 CP, degree of deacetylation =  ...  N,N-dimethylformamide (DMF) were dried over CaH2."
3851,10.1016/j.polymer.2010.12.052,something_else,"For investigation of the drug release, the resulti ... ge values based on three independent measurements."
3852,10.1016/j.tetlet.2010.03.011,something_else,"Stereoselective synthesis of the steroid core 11 i ... he first-generation synthesis (9.2%, nine steps).3"
3853,10.1016/j.actbio.2013.03.019,something_else,The other subcutaneous bilateral injection was rem ... different cantilever geometries for all hydrogels.
3854,10.1016/j.memsci.2006.09.008,something_else,PSS supports were cleaned before activation and el ... ited using the bath compositions shown in Table 2.
3855,10.1016/j.cattod.2011.11.011,something_else,"All reagents were analytical grade. Phenol, formal ... lyst 15 were purchased from Sigma-Aldrich Company."
3856,10.1016/j.msea.2013.05.005,something_else,Olympus BX51 with 200 times magnifications was use ... h were additionally etched with 2% nital solution.
3857,10.1016/j.msea.2013.05.005,something_else,"Commercially-available low-carbon steel with the c ... 3 and 1300 mm, respectively, was finally prepared."
3858,10.1016/j.sse.2012.11.010,something_else,Simple metal-insulator-silicon (MIS) capacitor str ... be easily extracted from the simple MIS structure.
3859,10.1002/jcp.21266,something_else,"The half-medium liquid was changed weekly. After 5 ... f the content of LTC-IC (Dexter and Lajtha, 1974)."
3860,10.1002/jcp.21266,something_else,"BM aspirate was initially collected into a tube co ... lan, Italy) and cultured until stromal confluence."
3861,10.1002/jcp.21266,something_else,"MSCs were cultured in 24-well plates in RPMI, supp ... F-1α (Ray Biotech, Inc., Norcross, GA) expression."
3862,10.1002/jcp.21266,something_else,"After 6 h incubation, the slides were rinsed with  ... ntibody anti-mouse IgG (Santa Cruz Biotechnology)."
3863,10.1016/j.memsci.2006.09.008,something_else,Porous stainless steel plates (PSS plates) and cup ... ld be found on the surface of the porous supports.
3864,10.1002/jcp.21266,something_else,"In these sets of experiments, PDL-MSCs cultures we ... ntrol) (Santa Cruz Biotechnology; Santa Cruz, CA)."
3865,10.1002/jcp.21266,something_else,"To induce osteogenic differentiation the sub-confl ... chsin and toluidine blue (Piattelli et al., 1997)."
3866,10.1002/jcp.21266,something_else,"On the second passage glass-adherent cells were fi ... 010 electron microscope (JEOL Ltd., Tokyo, Japan)."
3867,10.1016/j.jnucmat.2006.02.087,something_else,A small portion of the solid phase reaction produc ... sruhe and Gmelin-Institut fur Anorganische Chemie.
3868,10.1016/j.jnucmat.2006.02.087,something_else,Becquerelite was obtained by dissolving 0.42 g of  ... on of becquerelite is represented by the reaction:
3869,10.1016/j.surfcoat.2003.09.044,something_else,Disk-shaped (16 mm diameter; 1.5 mm thick) single- ... nce plays a critical role in component durability.
3870,10.1016/j.memsci.2006.09.008,something_else,Another aspect of this study was to study the poss ...  similar observations from numerous other samples.
3871,10.1016/j.memsci.2006.09.008,something_else,A detailed microstructure analysis was performed i ... ig. 5a showing the 0.5 μm grade blank PSS support.
3872,10.1016/j.memsci.2006.09.008,something_else,The intermetallic diffusion barrier of PSS support ... osition process is graphically depicted in Fig. 1.
3873,10.1002/jcp.21266,something_else,"To induce adipogenic differentiation, 20 x 103 cel ... rast phase microscopy (Pierdomenico et al., 2005)."
3874,10.1016/j.cattod.2011.11.011,something_else,"Magentically active ordered mesoporous resin (MOMR ... signated as MOMC-SO3H and MOMR-SO3H, respectively."
3875,10.1016/j.molcata.2006.11.028,something_else,FE-SEM images of TiO2 samples prepared through est ... NP-1); (b) 1.0 mmol (TNP-4); (c) 2.0 mmol (TNP-5).
3876,10.1016/j.molcata.2006.11.028,something_else,IR spectra of dried TiO2 samples prepared using PE ... G. The molar ratio of added water to TTIP was 200.
3877,10.1016/0021-9517(84)90027-7,something_else,Conversion of aqueous methanol over H-ZSM-5 zeolit ... A mechanism for the organic reactions is proposed.
3878,10.1016/j.msea.2013.02.013,something_else,The copper-solder-copper joints were prepared by i ... the push-off method at a loading rate of 1 mm/min.
3879,10.1016/j.msea.2013.02.013,something_else,The wetting of the copper substrate was studied by ... ting angle was measured using a personal computer.
3880,10.1016/j.msea.2013.02.013,something_else,The Perkin-Elmer DSC7 differential scanning calori ...  atmosphere were used. The sample mass was ~10 mg.
3881,10.1016/j.msea.2013.02.013,something_else,A series of lead-free Sn100-xBi10Agx solders with  ... analysis was Oxford Instruments INCA version 4.15.
3882,10.1002/asia.200700142,something_else,The per-NH2-α- and -β-CD used were the same as tho ... tinction coefficients at the Soret bands of hemin.
3883,10.1016/j.sse.2010.03.008,something_else,"A p-type Si (1 0 0) wafer with dopant concentratio ... d by high energy ions, no Ar ion milling was used."
3884,10.1016/j.msea.2015.07.046,something_else,"In the experiments, mass loss (ML) and mass loss r ... a more effective means of FWR improvement than LM."
3885,10.1002/bit.24431,something_else,"Human recombinant IL-7 was purchased from Cell Sci ... purchased from Fisher Scientific (Pittsburgh, PA)."
3886,10.1016/j.msea.2015.07.046,something_else,RCF tests are performed on a self-controlled man-m ...  repetitive tests on a given fabricated condition.
3887,10.1016/j.msea.2015.07.046,something_else,"A gray cast iron (supplying by Shenyang machine to ... alled amorphous carbon, as illustrated in Fig. 1b."
3888,10.1016/j.jelechem.2008.08.006,something_else,The electrolytic solutions were prepared with supr ... tammograms of freshly annealed Pd single crystals.
3889,10.1016/j.jelechem.2008.08.006,something_else,Spherical Pd single crystal (3 mm in diameter) was ... the transfer to the working electrode compartment.
3890,10.1016/j.cattod.2011.11.010,something_else,The NOx reduction performance of the (HC + OHC)/SC ... ard experimental conditions are listed in Table 2.
3891,10.1016/j.cattod.2011.11.010,something_else,The double layer catalytic monolith reactor contai ... C overnight and then calcined at 550 degC for 5 h.
3892,10.1016/j.cattod.2011.11.010,something_else,The cordierite substrates were then washcoated wit ... the internal channels of the cordierite substrate.
3893,10.1016/j.cattod.2011.11.010,something_else,The single-layer catalytic monolith reactors were  ... re ground in a ball mill with ZrO2 balls for 24 h.
3894,10.1016/j.cattod.2011.11.010,something_else,The Ag/Al2O3 catalyst was prepared by the incipien ... yed in the rear bed of the dual-bed configuration.
3895,10.1016/j.msea.2015.07.046,something_else,"The blocks with 5 mm of thickness, 15 mm of width  ... 7 J/mm2, 6.84 J/mm2, and 4.75 J/mm2, respectively."
3896,10.1016/j.molcata.2006.11.028,something_else,Pore size distribution of the TiO2 samples prepare ... NP-3); (d) 1.0 mmol (TNP-4); (e) 2.0 mmol (TNP-5).
3897,10.1002/bit.24431,something_else,PLGA microparticles encapsulating human recombinan ... e washed with PBS four times before freeze drying.
3898,10.1002/bit.24431,something_else,"In vitro release study was carried out by dividing ... ow cytometer (BD Biosciences, Franklin Lakes, NJ)."
3899,10.1016/j.molcata.2006.11.028,something_else,XRD patterns of TiO2 samples prepared through este ... NE-2); (c) 0.5 mmol (TNE-3); (d) 1.0 mmol (TNE-4).
3900,10.1016/j.molcata.2006.11.028,something_else,"For the photocatalytic decomposition of IMP, 60 mg ... to exclude the dispersion effect of the catalysts."
3901,10.1016/j.molcata.2006.11.028,something_else,A cylindrical Pyrex photoreactor equipped with a s ... light source was filtered out by the water jacket.
3902,10.1016/j.molcata.2006.11.028,something_else,TiO2 samples were synthesized by slowly dropping 0 ...  a rate of 1 K/min and then kept at 773 K for 2 h.
3903,10.1016/j.ijhydene.2008.09.008,something_else,Platinum surfaces were modified by ruthenium and t ... such as (θSn [?] 0.1) under saturation conditions.
3904,10.1016/j.ijhydene.2008.09.008,something_else,The 0.5 mM ruthenium-containing solution was prepa ... me potential region after each deposition process.
3905,10.1016/j.ijhydene.2008.09.008,something_else,The real surface area of pc platinum electrodes ra ... rchloric acid or 0.80 V in sulfuric acid solution.
3906,10.1016/j.ijhydene.2008.09.008,something_else,Electrochemical experiments were carried out at ro ... illiQ plus treated water (18.2 MΩ cm resistivity).
3907,10.1002/bit.24431,something_else,The loading efficiency was determined by mixing 10 ... rotein concentration as measured using this ELISA.
3908,10.1002/aenm.201100552,something_else,Poly(3-hexylthiophene) (P3HT) (purchased from Plex ... a Perkin-Elmer Lambda 12 UV/Vis spectrophotometer.
3909,10.1016/j.ica.2008.05.025,something_else,To an ethanolic solution (50 cm3) containing 1:2 m ... he composition [Cu(NO3)2(POC3H10N)2] was obtained.
3910,10.1016/j.jpowsour.2005.03.041,something_else,Fig. 1 shows the GC spectrum of the generated gas  ... oduced from EC and/or DMC decomposition on LiCoO2.
3911,10.1016/j.jpowsour.2005.03.041,something_else,Inductively coupled plasma (ICP) technique was use ... attery tester at a current density of 0.1 mA cm-2.
3912,10.1016/j.jpowsour.2005.03.041,something_else,Battery-grade ethylene carbonate (EC) and dimethyl ... fore it was characterized with various techniques.
3913,10.1016/j.jpowsour.2005.03.041,something_else,Nano-sized LiCoO2 was mixed with NH4OH in distille ... ting layer on nano-LiCoO2 particles was ca. 10 nm.
3914,10.1111/j.1600-0560.2006.00472.x,something_else,"This study was approved by the Ethical Committee f ... dissolved in the drinking water, until euthanasia."
3915,10.1002/bit.24431,something_else,"Upon sacrificing the mice, the spleens were remove ... ehyde and 200 uL of wash buffer for flow analyses."
3916,10.1002/bit.24431,something_else,All animal procedures were approved by the Institu ... he data to determine the statistical significance.
3917,10.1002/aenm.201100552,something_else,The current collecting grids were either inkjet pr ... h were measured at 5 different places of the grid.
3918,10.1016/j.ces.2013.07.050,something_else,"Oil-in-water (o/w) macro-emulsion was formed by mi ... , namely sodium dodecyl benzene sulphonate (SDBS)."
3919,10.1016/j.cattod.2011.11.011,something_else,"Before catalytic reactions, all catalysts were act ...  and the temperature of FID detector was 280 degC."
3920,10.1016/j.febslet.2009.12.029,something_else,DNA markers and restriction enzymes were obtained  ... rmed according to the manufacturer's instructions.
3921,10.1016/j.tsf.2005.04.123,something_else,The starting NDA-n2 solid was synthesized in a one ... product work-up have been previously reported [9].
3922,10.1016/j.tetlet.2010.03.014,something_else,"Further transformation of 7 to the (17R,18R,21R)-d ... ed C14-C24 fragment reported previously. 4b and 17"
3923,10.1016/j.carbon.2015.11.031,something_else,The rate capability for the freestanding Si nanopa ... enhance electronic transmission and ion diffusion.
3924,10.1016/j.carbon.2015.11.031,something_else,The fabrication procedure based on a one-step gel- ... alline Si nanoparticles in the composite membrane.
3925,10.1016/j.carbon.2015.11.031,something_else,Step one: Graphene oxide (GO) was synthesized from ... ding Si nanoparticles/graphene composite membrane.
3926,10.1016/j.jmatprotec.2006.07.020,something_else,Test specimens were machined into bars with dimens ... to characterize the microstructure of the samples.
3927,10.1016/j.poly.2008.09.004,something_else,"Benzene-1,2-dithiol (1.5 g, [?]10 mmol, Fluka 97%) ... cm-1), and λmax7 = 867.1 nm (ε = 23 345 M-1 cm-1)."
3928,10.1016/0005-2744(70)90184-1,something_else,A number of analogs of pteroylglutamyl-γ-glutamyl- ... ion of γ-glutamyl carboxypeptidase have been made.
3929,10.1016/j.tsf.2005.04.123,something_else,NDA-n2 thin films were deposited on substrates by  ... used silica substrates were cleaned using acetone.
3930,10.1016/j.jmatprotec.2007.10.082,something_else,The material used in the experiments was nodular c ... l composition of the material is given in Table 2.
3931,10.1016/j.apsusc.2009.10.109,something_else,The atomic concentrations calculated from XPS for  ... nnealed at 800 degC in nitrogen for 2 min and 2 h.
3932,10.1016/j.apsusc.2009.10.109,something_else,The surface morphologies of the films were observe ... ckness of ~6 nm calculated by the sputtering rate.
3933,10.1016/j.apsusc.2009.10.109,something_else,ZnO films were deposited on c-plane sapphire subst ... n a tube furnace under the protection of nitrogen.
3934,10.1007/s10854-016-4794-9,something_else,Aurivillius oxide Na0.5Bi2.5Ta2O9 inserted by Na0. ... tential application in optical temperature sensor.
3935,10.1016/j.elecom.2015.03.019,something_else,The fuel cell experiments were performed at 70 deg ... closed and tightened evenly with 10 kN force [14].
3936,10.1016/j.elecom.2015.03.019,something_else,The polycrystalline and (100) preferentially orien ... an from Alfa Aesar) were also used for comparison.
3937,10.1016/j.jmatprotec.2006.03.158,something_else,"During the hot forging of hollow products, the man ... nd that of the mandrel forging of tubes in Fig. 2."
3938,10.1016/j.jnucmat.2013.03.053,something_else,"During trapping experiments, the getter is placed  ... atography device was equipped with a TCD detector."
3939,10.1016/j.solmat.2010.12.050,something_else,"In this experiment, the OSCs were composed of P3HT ... e the transmittance of SU-8 film was over the 95%."
3940,10.1016/j.jnucmat.2013.03.053,something_else,Getters were prepared by mixing synthetic or comme ... e getters SSA will be assimilated to the MnO2 SSA.
3941,10.1016/j.jcis.2012.06.086,something_else,The photocatalytic activities were evaluated by th ... nitial intensity (C/C0) using a spectrophotometer.
3942,10.1016/j.jcis.2012.06.086,something_else,"XRD patterns of the obtained TiO2 products at 180  ...  oleic acid, HCl, and 0.8 ml of acetylacetone (f)."
3943,10.1016/j.ijhydene.2007.09.007,something_else,The stainless steels Fe-25Cr and Crofer 22 APU wer ... ying in air with a blow dryer prior to deposition.
3944,10.1016/j.fuel.2012.03.022,something_else,The esters rich phase was sampled at each temperat ... njected directly into the KF coulometric titrator.
3945,10.1016/j.fuel.2012.03.022,something_else,Biodiesels were characterized by GC-FID following  ... rrier gas was helium with a flow rate of 2 mL/min.
3946,10.1016/j.fuel.2012.03.022,something_else,The water solubility was measured in the biodiesel ...  the EN ISO 14214 limit for water was reached [7].
3947,10.1016/j.fuel.2012.03.022,something_else,"One of these purification steps is the fatty acid  ... m compounds, free fatty acid esters and soaps [8]."
3948,10.1002/ejoc.201300745,something_else,"Nitration of TTE: A 65 % HNO3 solution (55 μL, 0.1 ... fford unreacted 1a (40 %), 1g (16 %) and 1h (2 %)."
3949,10.1002/ejoc.201300745,something_else,"1-(5-Bromo-2-thienyl)-1,2,2-tri(2-thienyl)ethylene ... 3): calcd. C 49.65, H 2.55; found C 49.69, H 2.57."
3950,10.1002/ejoc.201300745,something_else,"1-(5-Formyl-2-thienyl)-1,2,2-tri(2-thienyl)ethylen ... 4): calcd. C 59.34, H 3.15; found C 59.01, H 3.17."
3951,10.1016/j.jcis.2012.06.086,something_else,TEM images of the TiO2 obtained at 240 degC (a); a ... n (a) and (f) are the magnifications of the edges.
3952,10.1002/ejoc.201300745,something_else,General Procedure for the Preparation of Tetrathie ... ounds 1a-d were purified by column chromatography.
3953,10.1002/ejoc.201300745,something_else,in which P and L are the integrated intensities of ... article size) with CH3CN/H2O (1 mL/min) as eluent.
3954,10.1002/ejoc.201300745,something_else,"General: Unless otherwise specified, all the react ... g lamp according to Equation (4) and Equation (5),"
3955,10.1002/ejoc.201300745,something_else,"Vilsmeier formylation was performed by using POCl3 ...  1g, which is a regioisomer of 1d, to be obtained."
3956,10.1007/s11661-007-9420-2,something_else,A salt spray test and electrochemical polarization ... f measured frequencies was from 10 mHz to 100 kHz.
3957,10.1007/s11661-007-9420-2,something_else,To elucidate the role of the primary β phase in th ... e Al-rich α phase remains on the as-cast die skin.
3958,10.1016/j.jpcs.2014.04.015,something_else,Calcium nitrate tetrahydrate (Ca(NO3)2*4H2O) and d ... chiometrically according to the reaction equation:
3959,10.1016/j.jcis.2012.06.086,something_else,"Besides oleic acid and HCl, additional acetylaceto ... role in the formation of the rutile crystal phase."
3960,10.1016/j.jcis.2012.06.086,something_else,"Remarkably, at 180 degC, the morphology of the TiO ... e product to be mainly anatase with little rutile."
3961,10.1002/ejoc.201300745,something_else,"vic-Bis(pinacolatoboryl)ethylene 2: Compound 2 was ... 4.70 ppm. 11B NMR (CDCl3, 100 MHz): δ = 30.04 ppm."
3962,10.1016/j.chemphys.2015.09.004,something_else,All compounds - di-t-butylperoxide (tBuOtBu) (Pfal ... nly after the spectral shape had fully stabilized.
3963,10.1016/j.jnucmat.2013.03.053,something_else,λ-MnO2 phase was obtained by ion exchange between  ... has Li0.06MnO2. λ-MnO2 is a pre-inserted material.
3964,10.1016/j.jnucmat.2013.03.053,something_else,""" NH 4 + -Cryptomelane'', was synthesized accordin ... icing that the structure contains water molecules."
3965,10.1002/app.25826,something_else,The in-plane internal stress of acrylate coatings  ...  The samples were produced in nitrogen atmosphere.
3966,10.1016/j.electacta.2008.02.087,something_else,ZnO electrode was prepared by incorporating slurri ... nO electrode and Ni(OH) 2 electrode was about 1:3.
3967,10.1016/j.jmatprotec.2006.03.157,something_else,The experiments were conducted using UNIMACRO 501C ... iments. The experimental setup is shown in Fig. 2.
3968,10.1002/adsc.201500799,something_else,"Thus, 2-pyridylMgCl[?]LiCl, which was prepared fro ... suppress immunity by inhibiting T cell activity.86"
3969,10.1002/adsc.201500799,something_else,"In the period 2007-2010, Olsson, Almqvist and co-w ... 20 degC for 1-4 min under microwave irradiation.76"
3970,10.1002/adsc.201500799,something_else,"Finally, some experiments were carried out to get  ... t KIE value (kH/kD=1.12) was obtained (Scheme 48)."
3971,10.1002/adsc.201500799,something_else,"The cross-coupling reactions, which were carried o ... es in 55% and 73% yield, respectively (Scheme 21)."
3972,10.1002/adsc.201500799,something_else,"The general procedure that was developed consisted ... ting from 0.25 mmol of heteroarenes 12, 13 and 18."
3973,10.1016/j.tetlet.2014.06.063,something_else,"Typical procedure for the E-selective HWE reaction ... t (2:1)] to afford (E)-9 (39 mg, 94%, E:Z = 95:5)."
3974,10.1016/j.msec.2011.09.003,something_else,Silanol groups are the predominant functional grou ... d redispersed in 200 ml of ethanol for future use.
3975,10.1016/j.msec.2011.09.003,something_else,"Following the Stober method, with some modificatio ... ispersion. The reaction mechanism is explained as:"
3976,10.1016/j.msec.2011.09.003,something_else,"Stock solutions of 1.28 M of FeCl3*6H2O, 0.64 M of ... the resultant dispersion was adjusted to 2.0 wt.%."
3977,10.1016/j.msec.2011.09.003,something_else,All of analytic reagents were purchased from the i ... nated by bubbling N2 gas for 1 h prior to the use.
3978,10.1016/0040-4039(96)00745-9,something_else,"1-O-Dimethoxytrityl-2,3-undecanediol: Dilithium te ... , dimethoxy and methine); 6.9-7.5 (2 m, 13, aryl)."
3979,10.1016/0040-4039(96)00745-9,something_else,"Dimethoxytrityl-R-glycidol: Dimethoxytrityl chlori ... OPh); 3.7 (s, 6, OCH3); 6.9 and 7.3 (m, 13, aryl)."
3980,10.1016/0040-4039(96)00745-9,something_else,"1-(Thymin-1-yl)-propane-2,3-diol: Thymine (4.2 g,  ...  with D2O); 6.2 (s, 1, thymine); 11.2 (bs, 1, NH)."
3981,10.1016/0040-4039(96)00745-9,something_else,"1-Imidazolyl-propane-2,3-diol: A solution of R-(+) ...  with D2O); 6.9, 7.1, and 7.6 (3 s, 3, imidazole)."
3982,10.1016/j.febslet.2009.12.029,something_else,High-molecular weight complexes formed by Dps1-Isp ...  (diluted 1:500) was used to detect the complexes.
3983,10.1016/j.msec.2011.09.003,something_else,"After stirring for 12 h, the obtained magnetic pro ... se, the induction period was approximately 30 min."
3984,10.1016/j.jnucmat.2013.03.053,something_else,"""Ag+-Cryptomelane'', was synthesized according to  ... is and lead to the Ag2Mn8O16 chemical formulation."
3985,10.1016/j.jpcs.2014.04.014,something_else,All reagents were of AR grades and obtained from S ... Ltd. (China). All chemicals were used as received.
3986,10.1016/j.matdes.2015.07.018,something_else,Three-point bending tests were carried out in acco ... cale parameter) were calculated according to [21].
3987,10.1016/j.jnucmat.2013.03.053,something_else,"""K+-Cryptomelane"", i.e. crypyomelane stabilized wi ... er. Final product has been determined as K2Mn8O16."
3988,10.1016/j.jnucmat.2013.03.053,something_else,"""Nsutite T"" was synthesized according to Thackeray ... .% H2SO4) which is stirred for 13 days at 40 degC."
3989,10.1016/j.jnucmat.2013.03.053,something_else,"""Nsutite P"" was synthesized according to Portehaul ... d product is dried at 25 degC under nitrogen flow."
3990,10.1111/j.1399-3011.1982.tb03025.x,something_else,"The octacosapeptide amide corresponding to the ent ... imum, owing to the mild basic and acid treatments."
3991,10.1111/j.1551-2916.2008.02737.x,something_else,"Differential thermal analysis (DTA) and thermograv ... d with a pH/ion meter (Corning Inc., Corning, NY)."
3992,10.1111/j.1551-2916.2008.02737.x,something_else,"Rare earth phosphates with rare earths of Gd, Tb,  ... ite or xenotime after heat treatment is discussed."
3993,10.1016/j.tsf.2015.01.038,something_else,"Thermo-gravimetric analysis (TGA) and differential ...  by using a Precision LCR Meter (E4980A, Agilent)."
3994,10.1016/j.tsf.2015.01.038,something_else,The KNN and KNN-La precursor solutions are deposit ... imes to achieve a total thickness of about 500 nm.
3995,10.1016/j.jpcs.2014.04.014,something_else,"Before preparing the BiVO4/MWCNT nanocomposites, m ... , and then dried under vacuum at 60 degC for 12 h."
3996,10.1016/j.jelechem.2014.11.034,something_else,The synthetic urine sample was prepared by dissolu ... f AML and VAL to achieve a required concentration.
3997,10.1016/j.jelechem.2014.11.034,something_else,"For sample preparation, 10 capsules containing com ... ntaining 10 mL of the BR buffer solution (pH 5.0)."
3998,10.1016/j.jelechem.2014.11.034,something_else,Stock solutions of AML and VAL at concentration of ... mounts of a 2.0 mol L-1 sodium hydroxide solution.
3999,10.1016/j.jelechem.2014.11.034,something_else,"Combined dosage forms samples used in this study w ... e in city of Londrina, state of Parana, in Brazil."
4000,10.1016/j.jelechem.2014.11.034,something_else,"Amlodipine (as besylate), valsartan, and sulfuric  ... lipore(r)) with resistivity greater than 18 MΩ cm."
4001,10.1016/j.jpcs.2012.04.015,something_else,"A polycrystalline sample of Nd2Cu0.8Ge3 with a tot ... r (Coulter Multisizer II, Beckman, Fullerton, CA)."
4002,10.1007/s11661-010-0332-1,something_else,Rods of PST-TiAl with a nominal binary composition ... M instruments have been used at 200 kV and 300 kV.
4003,10.1016/j.electacta.2007.02.026,something_else,"Deposits cannot be retrieved from the electrolyte, ...  common way of forming very pure and fine powders."
4004,10.1007/s11661-011-0801-1,something_else,"After testing, samples selected for metallographic ...  dried, and then furnace baked before examination."
4005,10.1016/j.jelechem.2014.11.034,something_else,"For the HPLC measurements, capsules were weighed a ...  retention times of 4.9 and 8.1 min, respectively."
4006,10.1016/j.optmat.2016.05.058,something_else,"As a representative example, a solution of vanilli ... ucts M1 and M2 were purified by recrystallization."
4007,10.1016/j.ces.2013.07.050,something_else,"The o/w emulsion was prepared synthetically by mix ...  the ratio, the greater is the emulsion stability."
4008,10.1016/j.apenergy.2015.11.010,something_else,"The diurnal dry-bulb air temperature cycle is calc ...  cycle during daytime and nighttime, respectively."
4009,10.1016/j.ijhydene.2007.09.006,something_else,"The Ti 0.8 Zr 0.2 V 2.7 Mn 0.5 Cr 0.8 Ni 1.75 allo ...  measured by a particle analyzer (Coulter210, UK)."
4010,10.1016/j.jelechem.2008.08.007,something_else,The environmental water samples were added with 5  ... ied in the analyses of Hg in environmental waters.
4011,10.1016/j.jelechem.2008.08.007,something_else,"A mixture of P4VP, PVC, THF and plasticizer (% w/w ... ing was the cell scheme of the proposed electrode:"
4012,10.1016/j.jelechem.2008.08.007,something_else,"Ion meter model 720 A and glass electrode 91-02 of ... mer, USA was used to study the membrane structure."
4013,10.1016/j.jelechem.2008.08.007,something_else,"P4VP with 6% ethylene dimethacrylate cross linked  ...  of Nalge, USA and kept at 4 degC when not in use."
4014,10.1016/j.surfcoat.2003.09.041,something_else,"θ/2θ XRD patterns of oxidised TiAlN/VN coating surfaces, heat treated in air at 670 degC for 1 h."
4015,10.1016/j.surfcoat.2003.09.041,something_else,"θ/2θ XRD patterns of oxidised TiAlN/VN coating surfaces, heat treated in air at 640 degC for 1 h."
4016,10.1016/j.surfcoat.2003.09.041,something_else,"θ/2θ XRD patterns of oxidised TiAlN/VN coating surfaces, heat treated in air at 600 degC for 1 h."
4017,10.1016/j.jmatprotec.2006.03.156,something_else,"The recycling of chips by conventional method cont ... mpaction, hot extrusion and cutting to final size."
4018,10.1016/j.surfcoat.2003.09.041,something_else,"GAXRD patterns of oxidised TiAlN/VN coating surfaces, heat treated in air at 550 degC for 1 h."
4019,10.1016/j.surfcoat.2003.09.041,something_else,"A SEM of the surface of an oxidised TiAlN/VN coati ...  sample 3, heat treated in air at 640 degC for 1 h"
4020,10.1016/j.surfcoat.2003.09.041,something_else,"A SEM of the surface of an oxidised TiAlN/VN coati ... sample 1, heat treated in air at 640 degC for 1 h."
4021,10.1016/j.surfcoat.2003.09.041,something_else,"A SEM of the surface of an oxidised TiAlN/VN coati ... sample 3, heat treated in air at 600 degC for 1 h."
4022,10.1016/j.surfcoat.2003.09.041,something_else,"A SEM of the surface of an oxidised TiAlN/VN coati ... sample 1, heat treated in air at 600 degC for 1 h."
4023,10.1016/j.surfcoat.2003.09.041,something_else,"A SEM of the surface of an oxidised TiAlN/VN coati ... sample 3, heat treated in air at 550 degC for 1 h."
4024,10.1016/j.surfcoat.2003.09.041,something_else,"A SEM of the surface of an oxidised TiAlN/VN coati ... sample 1, heat treated in air at 550 degC for 1 h."
4025,10.1016/j.jpowsour.2012.10.008,something_else,The bare and β-nickel hydroxide coated Al-substitu ... tage in the frequency range from 10 kHz to 10 mHz.
4026,10.1016/j.jpowsour.2012.10.008,something_else,"Al-substituted α-nickel hydroxide was prepared as  ...  Chemical Factory of Guangdong (Guangdong, China)."
4027,10.1016/j.surfcoat.2003.09.041,something_else,"A SEM of the surface of an oxidised TiAlN/VN coati ... sample 1, heat treated in air at 670 degC for 1 h."
4028,10.1016/j.bmc.2006.02.003,something_else,"DMSO, dimethylsulfoxide (J.T. Baker); MTT (Sigma); ... d naphthylethylenediamine dihydrochloride (Sigma)."
4029,10.1016/j.jmatprotec.2006.03.156,something_else,by hot extrusion of the cold compacted mixture of  ... plied after extrusion the hard phases are created;
4030,10.1016/j.msea.2007.11.068,something_else,The arc-melted buttons were cold rolled from 8.9 m ... ched into ice water (will be called ST hereafter).
4031,10.1016/j.ces.2013.04.020,something_else,Three photochemical experiments of one hour each w ... age molar rate of hydrogen production results from
4032,10.1016/j.ces.2013.04.020,something_else,"Two subsequent two runs of 3 h each were also cond ... lutions of 8.15 mmol and 12.35 mmol, respectively."
4033,10.1016/j.ces.2013.04.020,something_else,"After adding the electrolyte and catalyst, the rea ... formed entrains catalyst particles out of reactor."
4034,10.1016/j.ces.2013.04.020,something_else,During the experiments the magnetic stirrer has be ... experiment was of the order of Ncat[?]1012 grains.
4035,10.1016/j.ces.2013.04.020,something_else,A photocatalyst of solid-solution type has been pr ... catalyst has been an amount of 0.2% by weight PdS.
4036,10.1016/j.ces.2013.04.020,something_else,Note that differential Eqs. (21) and (22) in conju ...  the initial conditions can be written as follows:
4037,10.1016/j.ces.2013.04.020,something_else,Note that in a batch reactor the concentration of  ... e species concentrations are essentially constant.
4038,10.1016/j.elecom.2015.03.012,something_else,"Before each experiment, the Pt(111) electrode was  ... ut with the Pt(111) in the meniscus configuration."
4039,10.1016/j.msea.2007.11.068,something_else,Ti-8 mass% V and (Ti-8 mass%V)-4 mass%Sn alloys we ... enoted hereafter by nominal compositions in mass%.
4040,10.1007/s10853-015-9035-8,something_else,Human umbilical vein endothelial cells (HUVECs) we ... faces was calculated by Image J analysis software.
4041,10.1007/s10853-015-9035-8,something_else,"For protein adsorption studies, FITC-BSA was used  ... faces was calculated by Image J analysis software."
4042,10.1007/s10853-015-9035-8,something_else,The water contact angles were measured with a CA s ... ionalized silicon surface to check its uniformity.
4043,10.1007/s10853-015-9035-8,something_else,Average coating thickness of these coatings was me ... r layers had refractive indices of 1.45 at 632 nm.
4044,10.1007/s10853-015-9035-8,something_else,"The coatings were prepared by two steps: first, th ... , and then dried under N2 before characterization."
4045,10.1007/s10853-015-9035-8,something_else,"The substrates were washed as follows: silicon waf ... l aqueous solution, at a concentration of 2 mg/mL."
4046,10.1007/s10853-015-9035-8,something_else,"2-Methyl-2-oxazoline (MOXA, Aldrich, 98 %), 4-viny ... water used in this experiment was deionized water."
4047,10.1016/j.bbrc.2003.12.160,something_else,"The authors thank Kyowa Hakko Kogyo Co., Ltd. (Tok ... ) for providing the adriamycin used in this study."
4048,10.1016/j.bbrc.2003.12.160,something_else,"Quantitation of the accumulation of adriamycin in  ... meter (excitation, 472 nm; emission, 590 nm) [25]."
4049,10.1007/s10853-015-9035-8,something_else,"Fresh blood with 3.8 wt% sodium citrate anticoagul ... ng electron microscope (SEM, SIRION200, FEI, USA)."
4050,10.1016/j.ces.2013.04.020,something_else,"In addition, the above equation shows that approx. ... he flask and adding fresh, de-aerated electrolyte."
4051,10.1016/j.bmc.2006.02.003,something_else,Human peripheral blood mononuclear cells (HPBMC) w ... e medium was extrapolated from the standard curve.
4052,10.1016/j.bmc.2006.02.003,something_else,For growth inhibition assays 4 times 104 cells/mL  ... reference because of its potency on human models.7
4053,10.1016/j.tsf.2005.08.325,something_else,5-nm-thick Ni thin films used for the catalyst in  ... sity during the sputter deposition was 1.27 W/cm2.
4054,10.1016/j.scriptamat.2004.11.034,something_else,"Nanocrystalline Ni, Zr and Ti samples were prepare ... al value for the equivalent strain for rolling, ε."
4055,10.1016/j.tsf.2005.04.122,something_else,"In a typical preparation, 0.04 mmol of copper acet ... u-Kα radiation source employing 0.02deg step size."
4056,10.1002/chem.200304829,something_else,TDT was prepared under an atmosphere of N2: Cyanur ... n the one-step synthesis described in this report.
4057,10.1016/j.tetlet.2010.03.012,something_else,"Reagents and conditions: (a) 2,7-dibromopyrene, Pd ... b); (c) NH4OH, MeOH, rt, 24 h, 73% (4a), 81% (4b)."
4058,10.1016/j.tetlet.2010.03.012,something_else,"Reagents and conditions: (a) DMF diethyl acetal, M ... 4OH, MeOH, rt, 12 h, 70% (3a), 77% (3b), 78% (3c)."
4059,10.1016/j.fuel.2012.03.020,something_else,"The optimum experimental conditions of the hydroge ... g cat., and the purity of hydrogen is above 99.5%."
4060,10.1016/j.fuel.2012.03.020,something_else,The results above indicate that the optimum operat ...  in each hydrogen enrichment stage is above 99.5%.
4061,10.1016/j.tsf.2005.08.325,something_else,The morphology of the growing CNTs are related to  ... sured and averaged to obtain more accurate values.
4062,10.1016/j.fuel.2012.03.020,something_else,"In the subsequent sections, the operational condit ... n the output gas were the pertinent data analyzed."
4063,10.1016/j.fuel.2012.03.020,something_else,The quartz tube was filled and then placed in the  ... e inlet and outlet gas flow meters of the reactor.
4064,10.1016/j.fuel.2012.03.020,something_else,The carbonation/calcination kinetics of the sorben ... he runs. The gas flow rates were set to 50 mL/min.
4065,10.1016/j.fuel.2012.03.020,something_else,The B109-type Fe-based catalyst was crushed and si ... ed and sieved into particles 0.18-0.21 mm in size.
4066,10.1016/j.fuel.2012.03.020,something_else,The B109-type Fe-based catalyst containing the act ... m Beijing Pangshan Ceramic Colour Company (China).
4067,10.1002/jhet.2390,something_else,Bacterial cultures were grown in nutrient broth me ... e bacteria. The results are summarized in Table 1.
4068,10.1002/jhet.2390,something_else,The tested compounds were dissolved in DMF solvent ... were suspended in DMF and vortexed then processed.
4069,10.1002/jhet.2390,something_else,"To a solution of 6 2.76 g, (0.01 mol) in ethanol ( ... .14. Found: C, 49.08; H, 3.13; N, 17.64; S, 20.10."
4070,10.1002/jhet.2390,something_else,"A suspension of 6 (2.76 g, 0.01 mol), triethylorth ... .20. Found: C, 54.50; H, 3.56; N, 19.53; S, 11.24."
4071,10.1016/j.fuel.2012.03.020,something_else,"Once the hydrogen enrichment stage was completed,  ... nd promote the thermal decomposition of carbonate."
4072,10.1016/j.bmc.2006.02.003,something_else,Human peripheral blood mononuclear cells (HPBMC) w ...  specific cytotoxicity were calculated as follows:
4073,10.1016/j.tsf.2005.08.325,something_else,The CNTs were grown on the Ni/Cr samples at 400 de ... d to examine the binding states of the grown CNTs.
4074,10.1016/j.jelechem.2006.05.010,something_else,Boron doped diamond (BDD) films were grown on p-Si ... ith masking tape with an exposed area of 0.16 cm2.
4075,10.1016/j.bmc.2006.02.003,something_else,A mixture of the iodine derivative (18-21 and 31-3 ...  to give the title compounds collected in Table 1.
4076,10.1016/j.bmc.2006.02.003,something_else,A mixture of the chlorine derivative (14-17 and 27 ... ized from toluene to give the following compounds:
4077,10.1016/j.bmc.2006.02.003,something_else,"The ester derivative (23-26, 15 mmol) was refluxed ... ized from toluene to give the following compounds:"
4078,10.1016/j.bmc.2006.02.003,something_else,"A mixture of the allyl derivative (10-13, 20 mmol) ... ed and filtered to obtain the following compounds:"
4079,10.1016/j.bmc.2006.02.003,something_else,"A mixture of 3-hydroxy-4-allylxanthenone 918 or me ...  from EtOH, the following compounds were obtained:"
4080,10.1016/j.bmc.2006.02.003,something_else,"Reagents and conditions: (a) Br(CH2)nCl, K2CO3, ac ... ux; (d) piperidine or morpholine, toluene, reflux."
4081,10.1016/j.bmc.2006.02.003,something_else,"Reagents and conditions: (a) Br(CH2)nCl, K2CO3, ac ... ux; (d) piperidine or morpholine, toluene, reflux."
4082,10.1016/j.bmc.2006.02.003,something_else,"The synthesis of 3-alkoxyxanthones 1-4a,b is repor ... peridine or morpholine gave the desired compounds."
4083,10.1016/j.jelechem.2006.05.010,something_else,All reagents were of analytical grade and used wit ... avoid significant pH shifts in the bulk solutions.
4084,10.1016/j.molcata.2011.01.017,something_else,"The photocatalytic activity was estimated from the ...  flame ionization detector (GC 390B, GL Sciences)."
4085,10.1016/j.jcat.2012.10.030,something_else,"Activity measurements in the hydrogenation of CO2  ...  per milliliter catalyst per hour, were defined as"
4086,10.1016/j.jcat.2012.10.030,something_else,The basicity of the catalyst was measured by CO2 t ... quantitatively calibrated by injecting CO2 pulses.
4087,10.1016/j.jcat.2012.10.030,something_else,Temperature-programmed reduction (TPR) was carried ... r (TCD) was used to monitor the consumption of H2.
4088,10.1016/j.jcat.2012.10.030,something_else,The dispersion of Cu (DCu) and the exposed Cu surf ... a of the catalyst were calculated by the equations
4089,10.1016/j.matdes.2015.09.115,something_else,The samples were cut in transverse and longitudina ... yo 500-196-20 digital calliper as shown in Fig. 2.
4090,10.1016/j.matdes.2015.09.115,something_else,Laser deposition path to build the CLAD sample: th ... wing by a fourth shell-bead deposited around them.
4091,10.1016/j.matdes.2015.09.115,something_else,Ti-6Al-4V was used in form of wire or powder in th ... a 250 x 60 x 8 mm baseplate following this method.
4092,10.1002/anie.200601759,something_else,"In the dark (Bu4N)3[W(CN)8] (0.10 mmol) in MeCN wa ... H 2.71, N, 19.12; found: C 32.42, H 2.47, N 18.72."
4093,10.1016/j.ces.2013.07.050,something_else,"Diesel oil (density, ρ=830 kg/m3, viscosity, u=2.0 ... was used for the preparation of all o/w emulsions."
4094,10.1016/j.ces.2013.04.020,something_else,Simulations of batch mode of operation were perfor ... and the amount of dissolved hydrogen of 0.08 mmol.
4095,10.1016/j.ces.2011.05.019,something_else,"The Ag/HZSM-5 (Ag/HZ), Cu/HZSM-5 (Cu/HZ) and AgCu/ ... ay source (1486.6 eV) operated at 15 kV and 300 W."
4096,10.1016/j.jnucmat.2008.10.021,something_else,The pellets were mounted in Epon Resin 815 C therm ... roscope with SPOT diagnostics camera and software.
4097,10.1016/j.apsusc.2009.10.108,something_else,CV as well as LSV was performed with 5 mV s-1 volt ... e two sets of experiments were used for reporting.
4098,10.1016/j.apsusc.2009.10.108,something_else,"Polycrystalline Cu (99.999% pure, 0.95 cm diameter ... iments were controlled using LabVIEW(tm) software."
4099,10.1016/j.apsusc.2009.10.108,something_else,"As noted in the context of Eq. (5), Ta surfaces in ...  solution pH that controls the hydroxylated sites."
4100,10.1002/aoc.2957,something_else,"In a dry, two-necked, round-bottom flask were plac ... ance liquid chromatography (HPLC) chiral analysis."
4101,10.1002/aoc.2957,something_else,"In a dry, two-necked, round-bottom flask were plac ... was characterized by 1H, 11B and 13C NMR analysis."
4102,10.1002/aoc.2957,something_else,"Unless otherwise noted, all reactions were perform ... ere recorded on a Nicolet FTIR Nexus spectrometer."
4103,10.1002/aoc.2957,something_else,'On water' β-borylation of model alkynes (see supp ... 0 rpm. Isolated yield after column chromatography.
4104,10.1016/j.enzmictec.2013.02.010,something_else,All chemicals were obtained from commercial source ...  solutions of chemicals were stored in cool place.
4105,10.1002/aoc.2957,something_else,'On water' β-borylation of model alkenes (see supp ... 0 rpm. Isolated yield after column chromatography.
4106,10.1002/aoc.2957,something_else,"Standard conditions: 1.1 equiv. B2pin2, 3 mol% bas ... ted, pure water (2.5 ml), 27-30 degC, 800-900 rpm."
4107,10.1002/aoc.2957,something_else,"General reaction conditions: 1 (1.00 mmol), B2pin2 ... em). Method B: reaction was performed on pure H2O."
4108,10.1002/anie.200462226,something_else,We also produced multicomponent polymer-based bead ... gure 4 d). The mean size of the pores was 0.90 μm.
4109,10.1002/anie.200462226,something_else,Polymerization produced monodisperse solid particl ... h flow rates of the continuous phase (Figure 1 b).
4110,10.1016/j.jssc.2006.04.006,something_else,Ag0.8[W2O2Br6]: 24 mg (0.22 mmol) Ag powder (synth ... ction batches showed a Ag:W-ratio of 0.75+-0.15:2.
4111,10.1016/j.jssc.2006.04.006,something_else,"Hg0.55[W2O2Cl6]: 536 mg Hg (Heraeus, 99.999%) (2.7 ... . EDX measurements gave a Hg:W-ratio of 0.53(6):2."
4112,10.1016/j.jssc.2006.04.006,something_else,Pb0.55[W2O2Cl6]: 70 mg (0.25 mmol) dry PbCl2 and 1 ... rystals showed a constant Pb:W ratio of 0.45(2):2.
4113,10.1016/j.jssc.2006.04.006,something_else,"K0.84[W2O2Cl6]: 0.5 mmol (37 mg) dry KCl (Merck, 9 ... [WOCl5], according to X-ray powder diffractometry."
4114,10.1002/aoc.2957,something_else,'On water' β-borylation of Michael acceptors (see  ...  PPh3. Isolated yield after column chromatography.
4115,10.1016/j.jssc.2006.04.006,something_else,Tl0.98[W2O2Cl6]: 30 mg (0.25 mmol) dry TlCl (Aldri ... lack needles with a metallic luster were obtained.
4116,10.1016/j.enzmictec.2013.02.010,something_else,The carbon past electrode was prepared by hand mix ... s rinsed sufficiently with double distilled water.
4117,10.1016/j.enzmictec.2013.02.010,something_else,The 5 μl of 5 mg/ml enzyme stock solution was adde ... edure of the biosensor is illustrated in Scheme 1.
4118,10.1016/j.jnucmat.2011.08.018,something_else,"a: atomized, g: machined, h: γ-phase annealed at 8 ... 50 mm, t: as-fabricated foil thickness = 0.500 mm."
4119,10.1016/j.jnucmat.2011.08.018,something_else,The atomization technology widely used in powder m ... products between the fuel particles and Al matrix.
4120,10.1007/s11144-010-0170-6,something_else,"For the catalytic experiments, the powder was intr ... hrough a water-trap at 0 degC to remove the water."
4121,10.1016/j.jssc.2014.03.012,something_else,"Using high temperature solid-state techniques, 55  ... detected in the powder X-ray diffraction patterns."
4122,10.1016/j.jelechem.2014.11.035,something_else,"The measurements were performed ""in-situ"" using th ... ion of the implemented model can be found in [57]."
4123,10.1016/j.jelechem.2014.11.035,something_else,For the electrochemical impedance spectroscopy stu ... bbling with laboratory grade Argon (Linde Poland).
4124,10.1016/j.jelechem.2014.11.035,something_else,Polyelectrolytes used in our studies were polycati ...  Mili-Q water having the resistance of over 18 MΩ.
4125,10.1016/j.enzmictec.2013.02.010,something_else,A homogenous TEOS silica sol-gel was prepared by m ...  about one month when it was kept in refrigerator.
4126,10.1016/j.jelechem.2014.11.035,something_else,"The ability to form highly tailored polymer thin f ... xponentially growing films, containing more water."
4127,10.1002/jhet.2393,something_else,"The solution of 4-methyl-2-phenylthiazole-5-carbal ... h cold methanol, and recrystallized from methanol."
4128,10.1016/j.matchemphys.2016.05.036,something_else,The porous nanoalloy shells were formed via galvan ... dation is affected by the composition of emulsion.
4129,10.1016/j.matchemphys.2016.05.036,something_else,The effect of the copper-gold and drug-loaded copp ... experiment was repeated three times in triplicate.
4130,10.1016/j.matchemphys.2016.05.036,something_else,"To measure the release of doxorubicin, drug-loaded ...  was determined by measuring absorbance at 485 nm."
4131,10.1016/j.matchemphys.2016.05.036,something_else,"In DOX-loading experiments, the porous copper-gold ... us nanoparticles was estimated using the equation:"
4132,10.1016/j.matchemphys.2016.05.036,something_else,Copper-gold core/shell nanostructure was obtained  ... cles were separated and centrifuged several times.
4133,10.1016/j.matchemphys.2016.05.036,something_else,Copper nanoparticles (Cu NPs) were prepared by two ...  and washed by water and/or ethanol several times.
4134,10.1016/j.matchemphys.2016.05.036,something_else,Copper (II) sulphate pentahydrate (purity 99.995%) ... e reactions were performed by using Milli Q water.
4135,10.1002/jhet.2393,something_else,All the strains were obtained from microbial type  ... m was reported as MIC expressed in terms of ug/mL.
4136,10.1016/j.ces.2013.04.020,something_else,Predicted and measured hydrogen gas evolution for  ... ed radiation of 16 μmol photons/s (Velect=100 ml).
4137,10.1016/j.jssc.2006.04.006,something_else,"WOBr3 was prepared from W (Merck), WO3 (Fluka) and Br2 (Merck) as described in Ref. [6]."
4138,10.1016/j.actbio.2013.03.018,something_else,"Immunohistochemical staining was performed in acco ... equentially treated for 5 and 2 min, respectively."
4139,10.1002/aoc.2956,something_else,1H and 13C NMR (400 and 100 MHz) spectra were reco ...  compounds were used without further purification.
4140,10.1002/aoc.2956,something_else,"Reaction conditions: 1a (1 mmol), 2a (1 mmol), cop ... .1 mmol), base (2 mmol), solvent (3 ml), 110 degC."
4141,10.1002/aoc.2956,something_else,The results of several attempted cyclizations of 2 ... um in transition metal-catalyzed reactions.[17-27]
4142,10.1016/j.jmatprotec.2006.07.026,something_else,Magnesium alloy thick plate tends to fracture unde ... y plate coated steel plate is a reasonable method.
4143,10.1016/j.jmatprotec.2006.07.026,something_else,"Put the magnesium plate into chamber furnace, rais ... ng mold were heated to 150-300 degC, respectively."
4144,10.1016/j.jmatprotec.2006.07.026,something_else,"Then, AZ31B magnesium alloy thick plate (size 200  ... steel plate of 2 mm thickness, as shown in Fig. 3."
4145,10.1016/j.jmatprotec.2006.07.026,something_else,The experimental material was AZ31B magnesium allo ... equipment diagrammatic sketch was shown in Fig. 2.
4146,10.1016/j.solmat.2010.12.051,something_else,"All the dyes have been synthesized according to se ... by 1H NMR, 13C NMR, IR and MOLDI-TOF mass spectra."
4147,10.1002/aoc.2956,something_else,"To an organic reactor (Radleys Discovery Technolog ... ig. 1), all products are known.[6, 11, 16, 31, 32]"
4148,10.1016/j.solmat.2010.12.051,something_else,"In a 250 mL one-necked flask, 5 (0.46 g, 0.5 mmol) ... 1H49GaN6O5S m/z: calcd for 1046.27; found 1047.33."
4149,10.1016/j.solmat.2010.12.051,something_else,"In a 250 mL one-necked round-bottomed flask, a mix ... 3H52MnN5O4S m/z: calcd for 1029.31; found 1029.36."
4150,10.1016/j.solmat.2010.12.051,something_else,"A 50 mL CH3CN/CHCl3 solution of 4 (0.29 g, 0.34 mm ... (C61H51N5O2S) m/z: calcd for 917.38; found 918.35."
4151,10.1016/j.solmat.2010.12.051,something_else,"In a 100 mL three-necked flask, DMF (2.0 mL, 24 mm ... -TOF MS calcd for C58H50N4OS 850.37; found 850.33."
4152,10.1016/j.solmat.2010.12.051,something_else,"In a 500 mL three-necked flask, 4-methylbenzaldehy ... I-TOF MS calcd for C57H50N4S 822.38; found 822.40."
4153,10.1016/j.solmat.2010.12.051,something_else,"4-Bromobenzaldehyde (1.84 g, 10 mmol) and 1 (4.74  ... 28.44, 124.73, 120.50, 32.56, 28.44, 22.83, 16.01."
4154,10.1016/j.solmat.2010.12.051,something_else,Fluorine-doped SnO2 conducting glass (FTO) were cl ... t light (Pin) according to the following equation:
4155,10.1016/j.solmat.2010.12.051,something_else,1H and 13C NMR spectra were recorded with a Bruker ... which was used as an internal potential reference.
4156,10.1016/j.ces.2011.05.019,something_else,"(a) CO2 evolution with discharge time and (b) carb ... stage: F 2=60 ml/min, P discharge CSD = 2 . 3 W )."
4157,10.1016/j.solmat.2010.12.051,something_else,"In a 100 mL one-necked round-bottomed flask, a mix ...  4.80; N, 8.17. Found: C, 72.40; H, 4.87; N, 8.19."
4158,10.1016/j.jssc.2006.04.006,something_else,WOCl3 was prepared by reduction of WOCl4 with Al p ... p to 10 mol% in the products of different batches.
4159,10.1016/j.fuel.2014.12.014,something_else,The two microalgae B. braunii and N. gaditana were ...  for its characterization and further experiments.
4160,10.1016/j.fuel.2014.12.014,something_else,The fungus was inoculated 5 days before to start t ... croalgae lipids were distributed over the mycelia.
4161,10.1016/j.actbio.2013.03.018,something_else,"For protein extraction, re-epithelized tissue was  ... sed by the amount of total proteins in each group."
4162,10.1016/j.actbio.2013.03.018,something_else,HDFs were cultured in DMEM with LSGS and streptomy ... EGF by the amount of total proteins in each group.
4163,10.1016/j.actbio.2013.03.018,something_else,"The amount of released LPEI and phEGF from the MMP ... d by PicoGreen assay (λex = 480 nm, λem = 520 nm)."
4164,10.1016/j.actbio.2013.03.018,something_else,"phEGF was incorporated, at various nitrogen/phosph ... th of 480 nm and an emission wavelength of 520 nm."
4165,10.1016/j.actbio.2013.03.018,something_else,LPEI-immobilized NFs were fabricated using the sam ... peak intensity with the C1s or O1s peak intensity.
4166,10.1016/j.actbio.2013.03.018,something_else,Amine-terminated PCL-PEG diblock copolymer was syn ... mer was successfully synthesized (data not shown).
4167,10.1016/j.actbio.2013.03.018,something_else,"Poly(ε-caprolactone) (PCL; Mw 70,000-100,000) was  ... ntegrated DNA Technologies, Inc. (Coralville, IA)."
4168,10.1016/j.bmcl.2011.04.056,something_else,"Reagents and conditions: (i) (a) diisopropyl azido ... d, DCM, purified on Dowex(tm) 50WX8-200 resin, 5%."
4169,10.1016/j.fuel.2014.12.014,something_else,"The WCTB consisted in a Petri dish (90 mm of diame ... KH2PO4, 0.5 g/L MgSO4 7H2O and 1.5% agar, pH 7.4)."
4170,10.1016/j.bmcl.2011.04.056,something_else,A Mitsunobu reaction was also used to access compo ... n eluting with water followed by 9:1 MeoH/aq NH3).
4171,10.1016/j.apsusc.2007.10.077,something_else,"The MgO film of sample 2, which was heated to 650  ... wn during oxygen exposure at elevated temperature."
4172,10.1016/j.apsusc.2007.10.077,something_else,"In the first set of experiments, ~20 Å of MgO(1 1  ... uring growth and during post-deposition exposures."
4173,10.1016/j.apsusc.2007.10.077,something_else,"6H-SiC(0 0 0 1) (Cree, Inc.) substrates were degre ... d evacuated to a base pressure of 1.0 x 10-9 Torr."
4174,10.1016/j.fuel.2014.12.014,something_else,"Kinetics of FAAE production by R. oryzae for the t ... ed out at 20 degC, using ethanol as acyl acceptor."
4175,10.1016/j.fuel.2014.12.014,something_else,Identification and quantification of fatty acids i ...  were 250 degC and He was used as the carrier gas.
4176,10.1016/j.fuel.2014.12.014,something_else,An enriched agar patch inoculated with R. oryzae ( ... room temperature and were performed in triplicate.
4177,10.1016/j.fuel.2014.12.014,something_else,"To supply the alcohol to the bioreactor, an air fl ... sults obtained on alcohol evaporation experiments."
4178,10.1016/j.fuel.2014.12.014,something_else,"To improve mass transfer in the process, a three p ... gC; 96 h duration, N. gaditana lipids and ethanol."
4179,10.1016/j.bmcl.2011.04.056,something_else,"Reagents and conditions: (i) AcCl, MeOH, 95%; (ii) ... (iv) LiOH, aq THF, 78%; (v) 4 M HCl, dioxane, 95%."
4180,10.1016/j.jnucmat.2011.08.011,something_else,The positron source is a 22NaCl deposit on nickel  ... ecure them in position throughout the experiments.
4181,10.1016/j.optmat.2016.05.058,something_else,"Methode A: As a representative example, to a stirr ... was filtered and dried under vacuum for one night."
4182,10.1016/j.optmat.2016.05.058,something_else,Single-layer devices were elaborated as sandwich s ... es were recorded with a Keithley 236 source meter.
4183,10.1016/j.actbio.2013.03.013,something_else,"For in vitro sprouting angiogenesis assay, angioge ...  using MetaMorph computer image analysis software."
4184,10.1016/j.actbio.2013.03.013,something_else,For in vitro Matrigel(r) assay a 24-well plate was ... ections +- standard deviation of three replicates.
4185,10.1016/j.actbio.2013.03.013,something_else,"Poly(d,l-lactide-co-glycolide) (50:50) (PLGA) (Res ... ochloric acid were supplied by Carlo Erba (Italy)."
4186,10.1016/j.scriptamat.2011.10.031,something_else,The material studied with a nominal composition of ... + 59% methanol (vol.%) at -10 ~ -20 degC and 10 V.
4187,10.1016/j.jcat.2013.08.014,something_else,Titration of the sulfonated polymers is carried ou ... NaCl (aq) and stirred for 30 min before titration.
4188,10.1016/j.jcat.2013.08.014,something_else,Transmission electron microscopy (TEM) images are  ... stograms to depict the particle size distribution.
4189,10.1016/j.jcat.2013.08.014,something_else,Scanning electron microscopy (SEM) images and scan ... ections are transferred to a Cu/lacey carbon grid.
4190,10.1016/j.jcat.2013.08.014,something_else,In order to suspend the hydrophobic Pt/PDVB cataly ...  by high-performance liquid chromatography (HPLC).
4191,10.1016/j.jcat.2013.08.014,something_else,In order to suspend the hydrophobic Pt/PDVB cataly ... 1H nuclear magnetic resonances spectroscopy (NMR).
4192,10.1016/j.jcat.2013.08.014,something_else,"Gas-phase sulfonation of Pt/PDVB-dep and Pt/PDVB-i ...  briefly with THF 1, and dried as described above."
4193,10.1016/j.jcat.2013.08.014,something_else,For depositing 1 wt% of platinum preferentially on ... ount of platinum precursor is changed accordingly.
4194,10.1016/j.jcat.2013.08.014,something_else,"Silica gel was acquired from Sigma-Aldrich as TLC  ... ied out in oxygen (Air Liquide, 99.5%) atmosphere."
4195,10.1007/s00339-011-6750-0,something_else,All the samples were polished to 0.3 mm in thickne ... wn to room temperature. This is the aging process.
4196,10.1002/cssc.201301152,something_else,A PEDOT:PSS (CLEVIOSTM PH) dispersion was diluted  ...  a UV-curable epoxy resin in a N2-filled glovebox.
4197,10.1002/cssc.201301152,something_else,[a] P3HT:PCBM films were dried promptly in a circu ... imize the PCE as a result of a slow drying effect.
4198,10.1016/j.watres.2008.07.035,something_else,"Titanium oxide (rutile, 1317-80-2), copper sulphat ... purchased from Sigma Aldrich and used as received."
4199,10.1016/j.watres.2008.07.035,something_else,The helium stream at outlet of the reactor was the ... ide through the precipitation of barium carbonate.
4200,10.1016/j.actbio.2013.03.013,something_else,Collagen matrices activated with VEGF or VEGF/Hp ( ... solution (70 ng ml-1 of VEGF) at 37 degC for 24 h.
4201,10.1016/j.actbio.2013.03.013,something_else,In vitro release profile of VEGF from collagen mat ... s collected from three different batches (for Hp).
4202,10.1016/j.actbio.2013.03.013,something_else,"PLGA microspheres containing VEGF/Hp (0.1 μg of VE ... rospheres, respectively) were produced as control."
4203,10.1016/j.actbio.2013.03.013,something_else,VEGF loaded microsphere shape and morphology were  ... on a metal stub and coated with gold under vacuum.
4204,10.1016/j.tetlet.2003.08.093,something_else,A representative procedure is given here: A soluti ... acterized by NMR spectroscopy and FAB-MS analysis.
4205,10.1016/j.tetlet.2003.08.093,something_else,"Herein we report that the bismuth triflate (5 mol% ... ent with that reported in the literature. 22., and"
4206,10.1016/j.cej.2014.11.034,something_else,"During the biomedical tests, the H1975 lung cancer ... tical signals for counting and detection purposes."
4207,10.1016/j.cej.2014.11.034,something_else,Fig. 3 illustrates the schematic diagram of the mi ...  and then stored as a file on a personal computer.
4208,10.1016/j.cej.2014.11.034,something_else,"At the next stage, a mixture of PDMS prepolymer an ...  coated with the wet PDMS as glue before assembly."
4209,10.1016/j.cej.2014.11.034,something_else,Fig. 2 shows a picture of an assembled 3D Tesla mi ... of constraint of the standard lithography process.
4210,10.1016/j.jeurceramsoc.2017.01.008,something_else,Multi-wall carbon nanotubes with -COOH functional  ... nd repeated six times to get homogeneous solution.
4211,10.1016/j.jeurceramsoc.2017.01.008,something_else,"So, in the present study, a series of MWCNTs/geopo ... sulting composites were compared and investigated."
4212,10.1016/j.watres.2008.07.035,something_else,In all the experiments the solution was preventive ...  to prevent the dissolution of atmospheric oxygen.
4213,10.1016/j.actbio.2013.03.013,something_else,VEGF release profile from microsphere-activated co ... ach gel +- standard deviation of three replicates.
4214,10.1016/j.actbio.2013.03.013,something_else,Angiogenic activity of entrapped VEGF was also eva ...  amount +- standard deviation of three replicates.
4215,10.1016/j.actbio.2013.03.013,something_else,The solution containing VEGF still entrapped into  ...  amount +- standard deviation of three replicates.
4216,10.1016/j.actbio.2013.03.013,something_else,"VEGF loaded microspheres (5.0 mg) were suspended i ... r 7, 14 and 21 days in release kinetic conditions."
4217,10.1016/j.actbio.2013.03.013,something_else,In vitro release of VEGF and Hp was evaluated in b ... s collected from three different batches (for Hp).
4218,10.1016/j.actbio.2013.03.013,something_else,Hp loading was evaluated on fluorescent VEGF-loade ... s at λex/λem = 342/438 nm as previously described.
4219,10.1016/j.actbio.2013.03.013,something_else,The amount of entrapped VEGF and BSA-Rhod within m ... metric assay at λex/λem = 553/577 nm for BSA-Rhod.
4220,10.1016/j.actbio.2013.03.013,something_else,"After running, gels were washed twice with water a ... d dipped in Azure II 0.008% to visualize Hp bands."
4221,10.1016/j.actbio.2013.03.013,something_else,Native electrophoresis analysis were carried out b ... DS and 10% 2-mercaptoethanol to the sample buffer.
4222,10.1016/j.actbio.2013.03.013,something_else,Collagen matrices activated with VEGF-loaded micro ... solution (70 ng ml-1 of VEGF) at 37 degC for 24 h.
4223,10.1016/j.watres.2008.07.035,something_else,The pH was regulated with perchloric acid and sodi ... sic or sodium sulphate were added to the solution.
4224,10.1016/j.watres.2008.07.035,something_else,The power of the lamp at 305 nm I(305) was 5.70 x  ... measured using a UV radiometer Delta Ohm HD 9021).
4225,10.1016/j.watres.2008.07.035,something_else,Experiments with UV lamp were carried out at 298 K ... aluminium foil and filled with 250 mL of solution.
4226,10.1016/j.cej.2007.11.014,something_else,The amount of CO and CO2 released was determined b ... ea under of the concentration curve versus volume.
4227,10.1016/j.cej.2007.11.014,something_else,The samples released tar and water during the firs ... e was reached using a heating rate of 20 degC/min.
4228,10.1016/j.cej.2007.11.014,something_else,"Five different commercial carbon black samples, XC ...  Norit sample presents the highest oxygen content."
4229,10.1016/j.jpowsour.2016.02.060,something_else,"XRD was performed using a D/Max, Rigaku apparatus  ... th a step time cut-off of 12.5 h during 20 cycles."
4230,10.1016/j.jpowsour.2016.02.060,something_else,"A piece of sodium metal (99.9%, Sigma Aldrich) was ...  sample (Sigma Aldrich) was used as the catholyte."
4231,10.1016/j.actamat.2015.09.055,something_else,Microstructure degradation of cermet anodes for so ... ickel grain growth in dry and in humid atmospheres
4232,10.1016/j.actamat.2015.09.055,something_else,Anode supported half cells were prepared as descri ... ully reduce the nickel oxide. No cathode was used.
4233,10.1016/j.msea.2012.01.047,something_else,"The ingots were homogenized at 920 degS for 5 h an ... reductions of 60% and 80% were used, respectively."
4234,10.1016/j.enconman.2012.07.013,something_else,Simulation of vertical U-tube ground-coupled heat  ... systems using the cylindrical heat source solution
4235,10.1016/j.msea.2012.01.047,something_else,"Three kinds of alloys were prepared: Cu-Cr, Cu-Cr- ... ots was analyzed by ICP-AES and listed in Table 1."
4236,10.1016/j.cattod.2013.03.039,something_else,"NH4 ZSM-5 zeolite (MFI structural type, Si/Al mola ... ysico-chemical properties are reported in Table 1."
4237,10.1016/j.tet.2007.06.063,something_else,Method A: To a stirred solution of α-epoxide 17 (1 ... d for C20H35O2 [M+H]+ 307.2637 and found 307.2640.
4238,10.1016/j.tet.2007.06.063,something_else,"A solution of 77% m-CPBA (23 mg, 0.134 mmol, 3 equ ... r C20H34 NaO2 [M+Na]+ 329.2456 and found 329.2462."
4239,10.1016/j.tet.2007.06.063,something_else,"Method A: A mixture of tosylate 12 (30 mg, 0.064 m ... for C20H34NaO [M+Na]+ 313.2507 and found 313.2519."
4240,10.1016/j.tet.2007.06.063,something_else,"To a stirred solution of exo-olefin 14 (40 mg, 0.1 ... for C18H30NaO [M+Na]+ 285.2194 and found 285.2195."
4241,10.1016/j.tet.2007.06.063,something_else,"A mixture of isopropyl ester 13 (80 mg, 0.167 mmol ... or C20H34NaO2 [M+Na]+ 329.2456 and found 329.2454."
4242,10.1016/j.tet.2007.06.063,something_else,"A solution of 77% m-CPBA (137 mg, 0.779 mmol, 3 eq ... r C27H42NaO5S [M+Na]+ 501.2650 and found 501.2654."
4243,10.1016/j.tet.2007.06.063,something_else,"p-TsCl (80 mg, 0.421 mmol, 1.3 equiv) was added, a ... r C27H42NaO4S [M+Na]+ 485.2701 and found 485.2700."
4244,10.1016/j.cattod.2013.03.039,something_else,"After reaction, the carbon content over spent cata ... ones previously determined by Guisnet et al. [26]."
4245,10.1007/s10853-012-6376-4,something_else,"The resin used in this study is a commercially ava ... carbon fiber, 10 oz/square yard, 6 k sized fabric."
4246,10.1016/j.electacta.2008.02.082,something_else,"The electrodeposition was carried out in a three e ... 4(sat.) reference electrode (MSE, 640 mV vs. SHE)."
4247,10.1016/j.matchemphys.2016.05.039,something_else,"Analytical reagents and distilled water were used  ... or use, and its composition was listed in Table 2."
4248,10.1016/j.apsusc.2011.08.060,something_else,The polycrystalline diamond films (including micro ... ere drawn out and cooled to room temperature (RT).
4249,10.1016/j.apcata.2007.06.014,something_else,Activity tests were carried out at 700 degC in a f ... of 20 ml/min of pure hydrogen for 3 h at 550 degC.
4250,10.1016/j.apcata.2007.06.014,something_else,Ni-Si (molar ratio 2:1) and Ni-Cu-Si (molar ratio  ... talysts were finally calcined at 450 degC for 8 h.
4251,10.1016/j.jeurceramsoc.2013.10.031,something_else,"Commercially available, high-purity Y2O3 powder (B ... nd a rectangular cross section of 3.5 mm x 1.0 mm."
4252,10.1016/j.bbamcr.2013.02.011,something_else,Exposure to LEF or extracellular acidification doe ... endent experiments where bars represent the range.
4253,10.1016/j.bbamcr.2013.02.011,something_else,Involvement of pH changes in EGFR phosphorylation. ... endent experiments where bars represent the range.
4254,10.1016/j.bbamcr.2013.02.011,something_else,"Electrochemically produced ROS following exposure  ... HA, as indicated, using regular two-tailed t-test."
4255,10.1016/j.bbamcr.2013.02.011,something_else,"Analysis of LEF-induced EGFR and ERK phosphorylati ...  0.001, relative to control, by one-sample t-test."
4256,10.1016/j.matchemphys.2016.05.039,something_else,"The specimens in ring form (thickness: 80 mm, oute ... in distilled water within the hour before testing."
4257,10.1016/j.bbamcr.2013.02.011,something_else,LEF induced EGFR and ERK phosphorylation in both C ...  viability as measured by FACS using PI exclusion.
4258,10.1016/j.bbamcr.2013.02.011,something_else,Changes in ROS level were determined using H2DCF-D ...  using WINMDI flow cytometry application software.
4259,10.1016/j.bbamcr.2013.02.011,something_else,"After exposure to the different stimuli, cells wer ... rce) according to the manufacturer's instructions."
4260,10.1016/j.bbamcr.2013.02.011,something_else,Total protein measurement was performed after cell ... rce) according to the manufacturer's instructions.
4261,10.1016/j.bbamcr.2013.02.011,something_else,Cell viability was detected using propidium iodide ... s using Elisa Reader as described previously [65].
4262,10.1016/j.bbamcr.2013.02.011,something_else,The measurement of the medium's pH in the three co ... ntral compartment and pH >= 10 in the cathode one.
4263,10.1016/j.bbamcr.2013.02.011,something_else,"In selected experiments, cells were pre-incubated  ... M + 25 mM Hepes at pH 7.4 before Western Blotting."
4264,10.1016/j.bbamcr.2013.02.011,something_else,"COS5-7 (fibroblast-like cells), African green monk ...  in serum-free DMEM at room temperature for 5 min."
4265,10.1016/j.bbamcr.2013.02.011,something_else,Phospho-EGF receptor (Tyr1173) (53A5) rabbit mAb w ... inimidyl) suberate (BS3) was obtained from Pierce.
4266,10.1016/j.bbamcr.2013.02.011,something_else,"After different treatments, cells were washed with ... 5) followed by a secondary antibody linked to HRP."
4267,10.1007/s10853-012-6376-4,something_else,Flexural tests under three-point bend configuratio ...  materials were prepared for static flexure tests.
4268,10.1007/s10853-012-6376-4,something_else,The aluminum plate was laid on a flat surface and  ... the same method to compare with nanophased system.
4269,10.1007/s10008-011-1623-1,something_else,"In this study, we utilized Al nanoparticles in epo ... py (FIB- TEM) after wet/dry cyclic corrosion test."
4270,10.1016/j.cattod.2012.03.081,something_else,"In a 50 ml double neck RB equipped with a magnetic ... eparately listed, if clear separation is obtained."
4271,10.1016/j.cattod.2012.03.081,something_else,ethyl 2-oxo-2-p-tolylacetate was prepared accordin ... give the α-keto acid (2-oxo-2-p-tolylacetic acid).
4272,10.1016/j.cattod.2012.03.081,something_else,In a 100 ml double neck RB equipped with a magneti ... ate mixture to obtain the product 1j in 30% yield.
4273,10.1016/j.cattod.2012.03.081,something_else,"In a 50 ml RB flask, ethyl 2-oxo-4-phenylbutanoate ... cetate mixture to give the product 1i (30% yield)."
4274,10.1016/j.cattod.2012.03.081,something_else,"C. parapsilosis ATCC 7330 was purchased from ATCC  ... ometer operating at 500 and 125 MHz, respectively."
4275,10.1016/j.fuproc.2015.01.014,something_else,Changes in biodiesel properties were monitored by  ... the use of SUPELCO FAME-mix 18 component standard.
4276,10.1016/j.fuproc.2015.01.014,something_else,A microcosm test was constructed to study corrosio ... sks. Experimental test matrix is given in Table 2.
4277,10.1016/j.fuproc.2015.01.014,something_else,Corrosion tests were executed according to the rec ... ights of cleaned coupons was registered to 0.1 mg.
4278,10.1016/j.cattod.2012.03.081,something_else,(i) Racemic mandelamide rac-4a and its ring substi ... ts corresponding optically pure compounds R-4a-4e.
4279,10.1016/j.conbuildmat.2016.03.143,something_else,Methodology for the mix design of self-compacting  ... rent mineral additions in binary blends of powders
4280,10.1016/j.cej.2013.08.003,something_else,A stable emulsion of uniformly small water droplet ... one hour larger droplets became visible (Fig. 9d).
4281,10.1016/j.cej.2013.08.003,something_else,The organic droplets were cured and dried to allow ... n epoxy resin and fracturing the hardened samples.
4282,10.1016/j.cej.2013.08.003,something_else,"In order to analyze particle vesiculation and morp ... se, the samples were sputtered with gold/platinum."
4283,10.1016/j.cej.2013.08.003,something_else,"A two-step MVPs production was also implemented, i ... ed stirring for 15 min with a helix-type impeller."
4284,10.1016/j.cej.2013.08.003,something_else,"Both organic and aqueous phases were characterized ... evice Dataphysics OCA 20, being equal to 1.5 mN/m."
4285,10.1016/j.cej.2013.08.003,something_else,The same composition of the organic and aqueous ph ... roxide and 0.02 wt.% ammoniacal ferrous sulphate).
4286,10.1016/j.cej.2013.08.003,something_else,Unsaturated polyester was provided by Resiquimica  ... re supplied by Sigma-Aldrich and used as received.
4287,10.1016/j.cej.2013.08.003,something_else,Multivesiculated polyester particles (MVPs) have b ... n incorporation in non-matte coatings is intended.
4288,10.1016/j.conbuildmat.2016.03.143,something_else,Methodology for mix design of the mortar phase of  ... rent mineral additions in binary blends of powders
4289,10.1002/smll.201402756,something_else,Water Splitting Experiments: All the water splitti ... 1 mmol mL-1 KH2PO4 aqueous solution with pH = 7.0.
4290,10.1016/j.cattod.2012.03.081,something_else,"C. parapsilosis ATCC 7330 was grown in yeast malt  ... er (pH 7.2, 10 mM) and used for biotransformation."
4291,10.1016/j.cattod.2012.03.081,something_else,6.4 g wet cells of C. parapsilosis ATCC 7330 was s ...  the reduction of remaining primary α-keto amides.
4292,10.1016/j.cemconres.2016.06.009,something_else,Standard mortars were prepared according to EN 196 ...  strength measurements (and one heat measurement).
4293,10.1016/j.cemconres.2016.06.009,something_else,Cement production essentially takes place in three ... rd cement from leaving the plant for the consumer.
4294,10.1016/j.ces.2014.05.019,something_else,"Heterogeneous nucleation of clathrates from superc ... ater mixtures, and the effect of an added catalyst"
4295,10.1016/j.ces.2014.05.019,something_else,Experimental temperature profiles. Conversion time ... elt until the whole drop has converted to hydrate.
4296,10.1016/j.ces.2014.05.019,something_else,A strain controlled rheometer (ARES-G2) with Couet ... til the measured viscosity reached a steady value.
4297,10.1016/j.ces.2014.05.019,something_else,Rheometric analysis was performed on density-match ... igible within the experimental times in this work.
4298,10.1016/j.ces.2014.05.019,something_else,"at -30 degC, another 10 μL water was put on top of ... ed in step 1, to form a taller columnar structure;"
4299,10.1016/j.ces.2014.05.019,something_else,Ice was formed by initially freezing 10 μL deioniz ... anchored at a 1 mm hole in the middle of the well;
4300,10.1016/j.cattod.2012.03.081,something_else,6.4 g wet cells of C. parapsilosis ATCC 7330 was s ...  were not isolated due to their low conversion/ee.
4301,10.1016/j.ces.2014.05.019,something_else,"In the single drop experiments, cyclopentane was t ... lved at 5% (w/w) in deionized water to form brine."
4302,10.1016/j.actamat.2016.10.064,something_else,The disk-shaped samples for TEM analysis were cut  ... on. The accuracy of EDX measurements was about 1%.
4303,10.1016/j.actamat.2016.10.064,something_else,The alloy was produced by continuous casting and t ... sulting billets were subjected to ECAP processing.
4304,10.1016/j.tetlet.2010.03.088,something_else,"Hydroxylamine hydrochloride (0.38 g, 5.5 mmol), tr ... , 6H), 7.95 (d, 2H), 7.75 (m, 12H), 1.80 (s, 36H)."
4305,10.1016/j.tetlet.2010.03.088,something_else,"We have adopted an one-pot, mild reaction conditio ... spectroscopy, and cyclic voltammetry (see Fig. 1)."
4306,10.1016/0040-4039(96)00644-2,something_else,"Commercial palladium on carbon (10%, Aldrich) was  ... ting at 180degC for 12 h under vacuum (10-1 Torr)."
4307,10.1016/j.jcis.2015.06.012,something_else,PPG-5-CETETH-20 (Procetyl(r) AWS) was purchased fr ...  extracted by hydrodistillation in the laboratory.
4308,10.1016/j.cattod.2012.03.081,something_else,Organic solvents have been reportedly used to impr ... e was used as the cosolvent for further reactions.
4309,10.1016/j.cattod.2012.03.081,something_else,The viability of the cells during the bioreduction ... s 5 mmol glucose and 24 h reaction time were used.
4310,10.1016/j.ces.2014.05.019,something_else,"In the rheological experiments, 5% (w/w) sodium ch ... operties of the materials are provided in Table 1."
4311,10.1016/j.tet.2007.06.063,something_else,An aqueous suspension of Raney Ni (4.25 g) was add ... r C20H36Na O2 [M+Na]+ 331.2613 and found 331.2625.
4312,10.1002/smll.201402756,something_else,Characterization. The powder X-ray diffraction (XR ...  Perkin Elmer/Spectrum GX FTIR Spectrometer (USA).
4313,10.1002/smll.201402756,something_else,Growth of Au Nanoparticles on CdS Nanocrystals: Br ... dispersed in toluene for further characterization.
4314,10.1016/j.nima.2007.07.027,something_else,The MIS (Au/SnO2/n-Si) structures used in this wor ...  the strong accumulation region for MIS structure.
4315,10.1016/j.solidstatesciences.2014.03.003,something_else,ITO and ZnO:Al films were deposited on non-alkali  ... ntrolled to obtain specific film surface features.
4316,10.1016/j.jpcs.2009.07.016,something_else,"Thin films of Ge (99.99%) were deposited on glass  ... 8, and 823 K at constant annealing time of 30 min."
4317,10.1002/cnma.201600096,something_else,"A 10 mL ethanol dispersion of PtCu nanosheets (con ... filtered, and analyzed by gas chromatography (GC)."
4318,10.1002/cnma.201600096,something_else,"In a typical synthesis of PtCu alloy nanosheets, 2 ... n and further purified by a water-acetone mixture."
4319,10.1002/cnma.201600096,something_else,"In a typical synthesis of PtCu alloy nanosheets, C ... d washed several times with water-acetone mixture."
4320,10.1016/j.wear.2013.08.009,something_else,Hydrogen generation from coupling reactions of sod ... um powder with aqueous solution of cobalt chloride
4321,10.1016/j.solmat.2005.04.010,something_else,ZnO thin films were prepared by chemical spray usi ... d using a scanning electronic microscope JEOL 35C.
4322,10.1002/cbin.10461,something_else,All protocols in the current study were approved b ...  in a 37degC tissue culture incubator with 5% CO2.
4323,10.1016/j.biomaterials.2010.01.026,something_else,"In general, oxygen permeation through silicone hyd ... example, 600 barrer for polydimethylsiloxane [32]."
4324,10.1016/j.biomaterials.2010.01.026,something_else,The captive-bubble method was used to determine th ... es for each sample and the average was calculated.
4325,10.1016/j.biomaterials.2010.01.026,something_else,The optical transparencies of the hydrogels swelle ...  was found to correspond to a thickness of 100 μm.
4326,10.1016/j.biomaterials.2010.01.026,something_else,"Thermal gravimetric analysis (TGA: ETSAR6000, TG/D ... 0 degC with a 10 degC/min temperature change rate."
4327,10.1016/j.biomaterials.2010.01.026,something_else,"Mixtures of SiMA, TEGDMA(1.0 mol % to SiMA), and D ... The preparation results are summarized in Table 1."
4328,10.1016/j.biomaterials.2010.01.026,something_else,Various proportions of SiMA and MPC (total monomer ...  polymerization results are summarized in Table 1.
4329,10.1016/j.biomaterials.2010.01.026,something_else,"MPC was obtained from NOF Co., Ltd., Tokyo, Japan. ... Ltd., and prepared under the recommended protocol."
4330,10.1007/s10008-011-1623-1,something_else,Equivalent circuit diagram for steel coated by epo ... est in 0.1 M NaCl solution for different durations
4331,10.1007/s10008-011-1623-1,something_else,The chemical composition of the CS specimens in ma ... d with distilled water and acetone before coating.
4332,10.1016/j.biomaterials.2010.01.026,something_else,A single protein adsorption test was conducted to  ...  using the same protein adsorption test procedure.
4333,10.1002/smll.201402756,something_else,Fabrication of photoelectrochemical cell (PEC) Dev ... efore it was used for water splitting experiments.
4334,10.1002/cbin.10461,something_else,To introduce local anesthetic-induced neuronal inj ... red for additional 24 h before further evaluation.
4335,10.1002/cbin.10461,something_else,"Three days after bupivacaine treatment, to measure ... length under control condition (0 mM bupivacaine)."
4336,10.1002/smll.201402756,something_else,"Chemicals: Cadmium chloride (CdCl2, 99.995%, Sigam ... ere used as received without further purification."
4337,10.1016/j.electacta.2007.02.062,something_else,DSC was carried out on a STA 409 PC instruments (N ... C thermograms during the programmed heating steps.
4338,10.1016/j.electacta.2007.02.062,something_else,"BMPyTFSI was prepared by anion exchange reaction f ... ), 1136 cm-1 (vs, δSO), 1058 cm-1 (vs, δC-F), etc."
4339,10.1016/j.electacta.2007.02.062,something_else,"PEO (Mw = 600,000, Aldrich), LiTFSI (Aldrich), 1-b ... ghai Reagent) were used as the starting materials."
4340,10.1016/j.msea.2012.01.045,something_else,At first the cement slurry was poured in to a slur ... n 10A standard [20] using the Fann 35 device [21].
4341,10.1016/j.msea.2012.01.045,something_else,"In order to verify free-fluid content an atmospher ... rcent free fluid, utilizing the following formula:"
4342,10.1016/j.msea.2012.01.045,something_else,Compressive strength was measured using Ultrasonic ... nd the load was applied with a rate of 72 +- 7 kN.
4343,10.1016/j.msea.2012.01.045,something_else,At first the slurry was loaded in to a slurry cont ... in and 30 min of the stirring period was reported.
4344,10.1002/cbin.10461,something_else,"Cultured DRG neurons were lifted and trypsinized i ... n a FACSCalibur cytometer (Becton Dickinson, USA)."
4345,10.1016/j.msea.2012.01.045,something_else,In foam cementing method nitrogen is injected in t ... Litecrete cement designed by Schlumberger Company.
4346,10.1016/j.matchemphys.2015.03.051,something_else,The phase identification and purity of the powder  ... as completely within the sample for all 2θ angles.
4347,10.1016/j.matchemphys.2015.03.051,something_else,To prepare the compound we used a traditional in a ... Ni2FeSbO6 did not form in this preparation method.
4348,10.1002/cbin.10461,something_else,"Effects of bupivacaine on neurite outgrowth and mi ... aine (*P < 0.05, as compared to 0 mM bupivacaine)."
4349,10.1002/cbin.10461,something_else,"As we showed apoptosis was induced in DRG culture  ... anner from 0.5 mM to 10 mM (Figure 2B, *P < 0.05)."
4350,10.1002/cbin.10461,something_else,"DRG neurons were extracted from 8-week old C57BL/6 ... on a dose-dependent manner (Figure 1C, *P < 0.05)."
4351,10.1002/cbin.10461,something_else,"Cultured DRG neurons were lifted and trypsinized i ... ham Biosciences, USA) per manufacturer's protocol."
4352,10.1002/cbin.10461,something_else,The mouse miRNA mimics Negative Control (miR-NC) a ... a in DRG neurons were examined by qRT-PCR in 24 h.
4353,10.1002/cbin.10461,something_else,"Cultured DRG neurons were lifted and trypsinized i ... for mmu-miR-26a, and GAPDH for PTEN, respectively."
4354,10.1016/j.msea.2012.01.045,something_else,"First, at room temperature Na2SiO3*9H2O (70 g) (Me ... s were removed by calcination at 570 degC for 8 h."
4355,10.1016/j.tet.2007.06.063,something_else,"To a solution of the aldehyde 10 (1.0 g, 2.10 mmol ...  in the oxidative cleavage of the diol mixture 6)."
4356,10.1016/j.tet.2007.06.063,something_else,"A solution of NaIO4 (0.968 g, 4.56 mmol, 1.5 equiv ... r C27H38NaO5S [M+Na]+ 497.2337 and found 497.2333."
4357,10.1016/j.tet.2007.06.063,something_else,"To a stirred solution of the tosylate 8 (3 g, 6.78 ... mL) and their individual spectral data were given."
4358,10.1016/j.jim.2007.11.008,something_else,Forty micrograms of total protein from each cancer ... nd developed using Super-Signal WestPico reagents.
4359,10.1016/j.jim.2007.11.008,something_else,PrEC cells were plated into 96-well flat bottom pl ...  Molecular Devices Vmax kinetic microplate reader.
4360,10.1016/j.jim.2007.11.008,something_else,Adherent PC-3 cells (~ 1.2 x 107 total) were block ... were additional rounds of PC-3 positive selection.
4361,10.1016/j.jim.2007.11.008,something_else,"PC-3 Fab library DNA (IgG1κ and IgG2aκ, 10 μg each ...  in a 3-mL syringe, then dialyzed into 1 L of PBS."
4362,10.1016/j.jim.2007.11.008,something_else,"After obtaining the Internal Review Board approval ... ch time, and repeated for a total of three rounds."
4363,10.1016/j.jim.2007.11.008,something_else,"Primary antibody, pre-bleeds, post-bleeds, subtrac ... lated using CellQuest software (Becton Dickinson)."
4364,10.1016/j.jim.2007.11.008,something_else,"Phycoerythrin (PE)-conjugated goat anti-mouse IgG, ... ptavidin were obtained from Pierce (Rockford, IL)."
4365,10.1016/j.apcata.2007.06.017,something_else,Extrudates comprising zeolite were exposed to at l ... lcination in air was performed as described above.
4366,10.1016/j.jorganchem.2012.03.034,something_else,1H and 13C NMR spectra were recorded on a Bruker A ... aldehyde (For details see supporting information).
4367,10.1016/j.apcata.2007.06.017,something_else,"Mixing of solids and HEC solution was always carri ... min, and where they were kept at 550 degC for 3 h."
4368,10.1016/j.apcata.2007.06.017,something_else,"In the extrusion experiments, the solids were empl ... nd AlPO4 matrix in the final, calcined extrudates."
4369,10.1016/j.jcis.2015.06.016,something_else,This work was partially supported by a Grant-in-Ai ... chno Co. Ltd. for the gift of TiO2 (A-100) sample.
4370,10.1016/j.jcis.2015.06.016,something_else,"First, after Au/TiO2 particles (0.10 g) had been p ... m the reaction chamber by using gas tight syringe."
4371,10.1016/j.jcis.2015.06.016,something_else,TiO2 or Au/TiO2 particles (0.1 g) were placed in a ... m the reaction chamber by using gas tight syringe.
4372,10.1016/j.jcis.2015.06.016,something_else,"Anatase TiO2 particles with different surface area ... coupled plasma spectroscopy (ICPS-7500, Shimadzu)."
4373,10.1016/j.ces.2009.09.032,something_else,After initial runs at 2% loading were performed to ... ing were performed to investigate reproducibility.
4374,10.1016/j.ces.2009.09.032,something_else,The required amount of catalyst and polyethylene w ... flow of 100 ml/min plus 20 ml/min protective flow.
4375,10.1016/j.jpowsour.2005.03.047,something_else,The unit cell was assembled by sandwiching the sep ... as cut-off at 20% of the initial constant current.
4376,10.1016/j.apcata.2007.06.017,something_else,The solids need to be suspended in a liquid in ord ... urpose. The dissolved HEC serves as a plasticizer.
4377,10.1016/j.jpowsour.2005.03.047,something_else,The novel porous separator (bare separator) based  ...  h to remove the residual solvent and water trace.
4378,10.1016/j.jorganchem.2012.03.034,something_else,4a or 4b (2 mmol) and 10 mL of anhydrous acetonitr ... under reduced pressure to yield the ligands L1-L4.
4379,10.1016/j.jorganchem.2012.03.034,something_else,"The chiral complex C1 (0.25 x 10-2 mmol) and 1,3-d ...  40:1) to afford the epoxide product in 82% yield."
4380,10.1016/j.fuproc.2015.01.015,something_else,"Before the reaction, the gas line was switched to  ... CH4 content in the outlet gas [27], [30] and [45]."
4381,10.1016/j.fuproc.2015.01.015,something_else,"Catalyst testing was carried out in a fixed bed mi ... or analysis (Agilent 7890, with TCD, FID and FPD)."
4382,10.1016/j.fuproc.2015.01.015,something_else,The QDB-5 series catalysts containing nominal K2O  ... some metal salts contacting the impregnation tank.
4383,10.1016/j.fuproc.2015.01.015,something_else,The new K containing SWGS catalysts were prepared  ... re x represents the K2CO3 content in the catalyst.
4384,10.1016/j.fuproc.2015.01.015,something_else,The Mg modified alumina support material was prepa ... pinel modified γ-Al2O3 is marked as Al2O3-MgAl2O4.
4385,10.1016/j.cemconres.2016.06.006,something_else,Carbonation profiles after 91 days of CO2 exposure ... btracted from the total measured CaCO3 quantities.
4386,10.1016/j.cemconres.2016.06.006,something_else,"The carbonation depths, as measured by the phenolp ... uare root time dependency (x = K t1/2) is assumed."
4387,10.1016/j.cemconres.2016.06.006,something_else,The pore structure of the mortars was characterize ...  corresponding to a minimum pore radius of 3.6 nm.
4388,10.1016/j.jorganchem.2012.03.034,something_else,"Under an Ar atmosphere, Mn(CF3SO3)2 (0.1 mmol) was ...  dried under vacuum to give the desired complexes."
4389,10.1016/j.cemconres.2016.06.006,something_else,"Carbonation depths were measured after 0, 7, 14, 2 ... mortar inhomogeneity originating from the casting."
4390,10.1016/j.cemconres.2016.06.006,something_else,The mortar bars were cast into 40 x 40 x 160 mm3 m ... lid ratio of 3:1 by volume at 20 degC for 91 days.
4391,10.1016/j.cemconres.2016.06.006,something_else,The compositions of the binders (Table 2) targeted ... ithin +- 5% of the flow of the reference P mortar.
4392,10.1016/j.cemconres.2016.06.006,something_else,The binders used in this study were made from a wh ...  was used to achieve similar flow for all mortars.
4393,10.1016/j.matlet.2014.12.036,something_else,"Decoloration: Adsorption of RhB was carried out in ... e, and C is the residual concentration of the dye."
4394,10.1016/j.matlet.2014.12.036,something_else,"Preparation: For preparation of CoPc@BC, following ...  and then rinsed three times with ultrapure water."
4395,10.1016/j.matlet.2014.12.036,something_else,A novel cobalt tetraaminophthalocyanine decorated  ... nanocomposite (CoPc@BC) was designed and prepared.
4396,10.1016/j.jorganchem.2012.03.034,something_else,"Reactions were carried out in 1.5 mL of CH3CN for  ... .25 mmol of substrate, 1 mol% C1, 1.2 equiv AcOOH."
4397,10.1016/j.jorganchem.2012.03.034,something_else,"Unless otherwise stated, reactions were carried ou ... one, 1 mol% catalyst, 1.2 equiv of peracetic acid."
4398,10.1016/j.cemconres.2016.06.006,something_else,After 91 days of hydration under the conditions gi ... e RH range of 40-70% for maximum carbonation [17].
4399,10.1016/j.fuproc.2015.01.015,something_else,The industrial operation results were obtained fro ... exit CH4 were recorded for comparison in parallel.
4400,10.1016/j.jnoncrysol.2010.03.037,something_else,Glass compositions prepared in this study were 60. ...  to optical quality prior to optical measurements.
4401,10.1016/j.memsci.2015.03.076,something_else,"Analyzing, by Eq.(13), a solution of seawater simu ...  increase the volumetric requirements of seawater."
4402,10.1016/j.jmbbm.2012.02.017,something_else,Hank's solution was used in the lubricated wear te ... ts were carried out at room temperature (25+-3deg)
4403,10.1016/j.electacta.2007.02.021,something_else,Rectangular samples (with dimensions 10 mm x 10 mm ...  of analytical grade reagents and distilled water.
4404,10.1007/s10854-015-3483-4,something_else,"For device preparation, the ZnO colloidal nanorods ... tive back electrode with active areas of 0.12 cm2."
4405,10.1007/s10854-015-3483-4,something_else,ZnO colloidal nanorods were prepared according to  ...  and the nanorod concentration was about 15 mg/mL.
4406,10.1007/s10854-015-3483-4,something_else,"Zinc acetate dehydrate [Zn(CH3COO)2*2H2O, purity 9 ... trogen gas, then treated with O2 plasma for 5 min."
4407,10.1016/j.tsf.2009.03.078,something_else,AlCrTaTiZr five-element HEAN films were deposited  ... as applied to the films in a vacuum of 10- 6 Torr.
4408,10.1016/j.jpowsour.2010.12.043,something_else,Another possible explanation from our observations ... s the need to use an oven for solvent evaporation.
4409,10.1016/j.jpowsour.2010.12.043,something_else,"In this study, we have investigated four different ... s that colloidal inks produce better performances."
4410,10.1016/j.matlet.2007.03.042,something_else,A Shimadzu Differential Thermal Analyzer was used  ... gC with a heating temperature rate of 10 degC/min.
4411,10.1016/j.jpowsour.2010.12.043,something_else,A thin layer of Nafion(r) solution (Nafion(r) dry  ... sides in H2 and air (1.2/2.2 stoics) respectively.
4412,10.1016/j.jpowsour.2010.12.043,something_else,All materials were used as received without any fu ... of 0.5 mg cm-2) were purchased from Fuelcellstore.
4413,10.1016/j.matlet.2006.06.060,something_else,Experimental results indicated that 90% of Ag tran ...  to Ag and its effect can be expressed as follows:
4414,10.1016/j.jcis.2015.06.014,something_else,Cu2O submicron and micron particles with different ...  by NH2OH[?]HCl according to the Eqs. (2) and (3):
4415,10.1016/j.jcis.2015.06.014,something_else,"There are many parameters, such as time, reactant  ... of the attractive p-type Cu2O oxide semiconductor."
4416,10.1016/j.jcis.2015.06.014,something_else,Comparison of the morphological features of Cu2O p ... l by an equimolar amount of NaOH to avoid etching.
4417,10.1016/j.jcis.2015.06.014,something_else,The examples in Fig. 4d and 4e clearly demonstrate ... les by adjusting the amount of the reducing agent.
4418,10.1016/j.jcis.2015.06.014,something_else,Effects of synthesis parameters on the microstruct ...  h in addition to the synthesis conditions of (d).
4419,10.1016/j.jcis.2015.06.014,something_else,PEC H2 evolution properties of as-fabricated Cu2O  ... MSE according to: URHE = UMSE + 0.654V + 0.059 pH.
4420,10.1016/j.jpowsour.2010.12.043,something_else,The MEA fabrication was carried out using the meth ... g Pt cm-2. The active area of all MEAs was 16 cm2.
4421,10.1016/j.engappai.2012.02.016,something_else,The heat rejected at the hot side of the cold stag ... sidering the heat balance at the interface of TECs
4422,10.1016/j.apsusc.2011.07.027,something_else,"In order to produce ZnO thin films, Zn was sputter ... s with 50, 100, and 200 nm thicknesses repeatedly."
4423,10.1016/j.biomaterials.2013.11.032,something_else,"PVP (0.02 mmol, 1.0 g), Gd2O3-OA (0.25 mmol, 5.0 m ...  final product was dispersed and kept in DI water."
4424,10.1016/j.memsci.2015.03.076,something_else,The uHmax represent the specific energy contained  ... e an infinite volume of dilute solution to obtain.
4425,10.1016/j.electacta.2008.02.083,something_else,The procedures to measure the erosion rate were as ... y the specimen surface area and the test duration.
4426,10.1016/j.electacta.2008.02.083,something_else,The passivation behavior for (a) 1045 and (b) 1018 ... y 2 was prepared by 0.1 M H3BO3 + 0.025 M Na2B4O7.
4427,10.1002/app.42711,something_else,Fourier transform infrared (FTIR) and Real-time Fo ... ng a Hitachi TM-1000 scanning electron microscope.
4428,10.1002/app.42711,something_else,Para-allyl ether phenol derivative of cyclophospha ... onstant weight in vacuum at 60degC under -0.1 MPa.
4429,10.1016/j.jeurceramsoc.2010.12.009,something_else,pH and temperature versus time for a 3 wt% AlN powder suspension in water at 22 degC.
4430,10.1016/j.tetlet.2012.03.097,something_else,General procedure for the synthesis of quinoxaline ... er and dried affording the corresponding products.
4431,10.1016/j.tetlet.2012.03.097,something_else,Another striking feature of BAHC catalyst was easy ... runs with a modest change in yield of the product.
4432,10.1016/j.biomaterials.2013.11.032,something_else,"Gadolinium acetate, oleic acid (OA), oleylamine, c ... cted with Dual-view Optima 5300 DV ICP-OES system."
4433,10.1016/j.tetlet.2012.03.097,something_else,"Next, we have extended this protocol for the tetra ... and 81% yields, respectively in 20 min (Scheme 2)."
4434,10.1016/j.tetlet.2012.03.097,something_else,"Reaction conditions: Benzil (1.0 mmol), o-phenylen ... 5 mol %), aqueous hydrotropic solution (5 mL), RT."
4435,10.1016/j.tetlet.2012.03.097,something_else,In the absence of any catalyst the product 3a was  ... t and enabled the rapid organic reaction in water.
4436,10.1016/j.elecom.2010.10.031,something_else,The working electrode had been cathodically pre-ch ...  910B electrochemical station at room temperature.
4437,10.1016/j.elecom.2010.10.031,something_else,A four-electrode system was used in the present wo ... r Fe2+- ions as the following reaction shows [19]:
4438,10.1016/j.biomaterials.2013.11.032,something_else,All animal work was carried out under IACUC ethica ... e scanned when the tumor size reached 150-200 mm3.
4439,10.1016/j.biomaterials.2013.11.032,something_else,"HK-2 proximal tubule epithelial cells (ATCC, CRL-2 ...  [OD of sample well/OD of positive control] x 100."
4440,10.1016/j.biomaterials.2013.11.032,something_else,Gd2O3-PVP and Gd2O3-OA-CTAB colloidal solutions we ... ine the release of Gd(III) from the nanoparticles.
4441,10.1016/j.biomaterials.2013.11.032,something_else,"Gd2O3-OA (0.25 mmol, 1.0 ml) stock solution in chl ... product was collected by immediate centrifugation."
4442,10.1016/j.tetlet.2012.03.097,something_else,"Reaction conditions: Diketone (1.0 mmol), diamine  ... .0 mmol), PTSA (5 mol %), 40% aq NaPTS (5 mL), RT."
4443,10.1016/j.cemconres.2016.06.009,something_else,"An I-Cal 2000 HPC (Calmetrix Inc., USA) isothermal ... alorimetric results are presented per gram binder."
4444,10.1016/j.fuproc.2015.01.015,something_else,"When unloading the industrial catalyst after use,  ... sivate the industrial catalysts before collection."
4445,10.1016/j.fuproc.2015.01.015,something_else,Table 1 shows the SWGS catalysts used in the same  ... s needed to increase the steam content in the gas.
4446,10.1016/j.cemconres.2009.12.003,something_else,"For comparison, hydrated pastes of OPC and the ind ... hesised for comparison with the sodium composites."
4447,10.1016/j.cemconres.2009.12.003,something_else,"After mixing, the geopolymer/cement blends were po ...  in sealed plastic bags until compressive testing."
4448,10.1016/j.cemconres.2009.12.003,something_else,The geopolymer matrix was prepared by mixing toget ... omparability with the sodium geopolymer used here.
4449,10.1016/j.cemconres.2009.12.003,something_else,The sodium aluminosilicate geopolymer matrix was p ... nalysis of the halloysite is presented in Table 1.
4450,10.1016/j.jpowsour.2005.03.046,something_else,Several Li1+yNixCo1-2xMnxO2 materials with differe ... starting raw material at 950 degC for 10 h in air.
4451,10.1016/j.jcat.2008.10.012,something_else,The spectra were recorded using a Bruker IFS 66 sp ... mission mode with 2 cm-1 resolution and 100 scans.
4452,10.1111/j.1471-4159.2007.05145.x,something_else,"For electron microscopy, mice were perfused and th ... atus, endoplasmic reticulum, and lysosomes system."
4453,10.1016/j.cemconres.2009.12.003,something_else,Samples for SEM were prepared by cutting with a di ... ing an EX23000BU energy dispersive X-ray analyser.
4454,10.1111/j.1471-4159.2007.05145.x,something_else,The tissues were homogenized in buffer containing  ... med in triplicate for confirmation of the results.
4455,10.1111/j.1471-4159.2007.05145.x,something_else,"Mice were implanted with microdialysis intracerebr ... ree injections of METH (5 mg/kg, i.p., 2 h apart)."
4456,10.1111/j.1471-4159.2007.05145.x,something_else,Mice were killed and their brains quickly removed  ... racellular volume unit (striatal microdialysates).
4457,10.1111/j.1471-4159.2007.05145.x,something_else,"Male C57Bl mice (8-month old, n = 50) were purchas ... by the Local Ethical Committee for Animal Studies."
4458,10.1016/j.jpowsour.2008.02.022,something_else,"The working electrodes, prior to the experiments w ... rface in ultra-sonic bath in ethanol during 5 min."
4459,10.1016/j.jpowsour.2008.02.022,something_else,Lead dioxide electrode was prepared on cylindrical ... th the current density of 2 mA cm-2 during 2000 s.
4460,10.1016/j.jpowsour.2008.02.022,something_else,Thin film PANI electrode was synthesized from 1.1  ... ode was further discharged at -0.6 V during 180 s.
4461,10.1016/j.elecom.2010.10.032,something_else,"In summary, copper sulfide nanowires have been pre ...  and a model was proposed to explain this finding."
4462,10.1016/j.elecom.2010.10.032,something_else,The nanowires were grown from a solution consistin ...  out with a Rigaku Multiflex X-ray diffractometer.
4463,10.1111/j.1471-4159.2007.05145.x,something_else,The left brain hemisphere from each mouse was eith ...  in paraffin as described in Fornai et al. (1999).
4464,10.1016/j.elecom.2010.10.032,something_else,"All electrochemical experiments were performed at  ...  with DI water, and then dried in a stream of air."
4465,10.1016/j.cemconres.2009.12.003,something_else,Compressive strength measurements were made on 5-9 ... sting machine at a crosshead speed of 1 mm min- 1.
4466,10.1016/j.immuni.2012.12.007,something_else,(C) GM-DCs pretreated with 10 μg/ml piceatannol (P ... LISA. Data represent mean +- SD (n = 3) (A and C).
4467,10.1016/j.tet.2007.06.063,something_else,"To a solution of the alcohol 4 (3 g, 10.41 mmol) i ... lcd for C27H38NaO3S [M+Na]+ 465.2439 and 465.2435."
4468,10.1016/j.tet.2007.06.063,something_else,"A solution of NaIO4 (257 mg, 1.5 equiv, 1.21 mmol) ...  C20H31I NaO2 [M+Na]+ 453.1266 and found 453.1269."
4469,10.1016/j.tet.2007.06.063,something_else,To a stirred solution of the crude iodo derivative ... ane and their individual spectral data were given.
4470,10.1016/j.tet.2007.06.063,something_else,"To a stirred solution of abieta-7,13-dien-18-ol 4  ... 38.7, 39.7, 47.0, 50.7, 120.4 122.4, 135.5, 145.3."
4471,10.1016/j.tet.2007.06.063,something_else,All commercial chemicals were used without further ... e maintained unchanged through out all compounds.)
4472,10.1016/j.tet.2007.06.063,something_else,"Reagents and conditions: (a) i. Tf2O, pyridine, CH ... e3NO*2H2O, t-BuOH-H2O-pyridine, reflux, 48 h, 73%."
4473,10.1016/j.tet.2007.06.063,something_else,"In order to get the amberketal analog 2 the alcoho ... ide as co-oxidant (Scheme 4). 4, 4a, 4b, 4c and 4d"
4474,10.1016/j.tet.2007.06.063,something_else,"Reagents and conditions: (a) Raney Ni, THF, rt, 20 ... 4 h, 88%; (e) Tebbe's reagent, -10 degC, 2 h, 82%."
4475,10.1002/pssa.201330345,something_else,The GZO films were prepared by an rf magnetron spu ... ed behind the substrate holder and a thermocouple.
4476,10.1016/j.tet.2007.06.063,something_else,"Reagents and conditions: (a) p-TsCl, pyridine, 0 d ... 5 h, 85%; (d) excess NaI, DMF, 90 degC, 12 h, 50%."
4477,10.1007/s10008-010-1222-6,something_else,The electrode of NiO nanotubes was prepared accord ... 1 cm) current collector under a pressure of 8 MPa.
4478,10.1016/j.apsusc.2005.12.015,something_else,"SEM images of the film morphology for 5 ML, 12 ML, ... ages, scan size 1.6 μm x 1.6 μm), flux = 0.03 Å/s."
4479,10.1016/j.apsusc.2005.12.015,something_else,"Bismuth was deposited on the basal plane of HOPG ( ...  Å, the average distance between atoms in bulk Bi."
4480,10.1016/j.immuni.2012.12.007,something_else,Cells were fixed in 2% formaldehyde and 2% glutara ...  and operated at an acceleration voltage of 80 kV.
4481,10.1016/j.immuni.2012.12.007,something_else,OT-II transgenic CD4+ T cells (1 x 105) were cocul ... in the culture supernatants was analyzed by ELISA.
4482,10.1016/j.immuni.2012.12.007,something_else,Cells cultured on coverslips were fixed with 4% pa ... s were analyzed with a Keyence BZ-9000 microscope.
4483,10.1016/j.immuni.2012.12.007,something_else,Total RNA was isolated with the TRIzol reagent (In ... rs for 18 s rRNA were used as an internal control.
4484,10.1016/j.immuni.2012.12.007,something_else,"(I) GM-DCs pretreated with 20, 50, or 100 μg/ml of ... SA. Data represent mean +- SD (n = 3) (A-G and I)."
4485,10.1016/j.tet.2007.06.063,something_else,"To improve the overall yield of the aldehyde 7 fro ... d in the both Scheme 1 and Scheme 2, respectively."
4486,10.1016/j.fuproc.2015.01.015,something_else,"Test conditions: Dry syngas composition of CO 64.9 ...  ratio), temperature: 450 degC, pressure: 3.7 MPa."
4487,10.1007/s40553-014-0008-7,something_else,"XRD patterns of the SCTb, SCZY, and SZY particles  ...  pct CO2 (balance N2) for 3 h at 773.15 (500 degC)"
4488,10.1016/j.ssc.2012.04.034,something_else,In this section we describe recent progress in the ... centration and improve the flake-to-flake contact.
4489,10.1016/j.actbio.2015.02.030,something_else,"Human urothelial cells HTB4 (ATCC, Manassas, VA) w ... es between 3 and 10 were used for all experiments."
4490,10.1016/j.eurpolymj.2014.07.031,something_else,Fluorescence spectra of (a) 0.1 mg/ml FITC-ConA so ...  0.47 mg/ml of RITC labeled Glu-Mic nanoparticles.
4491,10.1016/j.eurpolymj.2014.07.031,something_else,Change in size distributions of nanoparticle aggre ... ispersions (nanoparticle concentration 0.1 mg/ml).
4492,10.1016/j.eurpolymj.2014.07.031,something_else,Fluorescence studies were conducted with a Horiba  ... nm) and rhodamine (580 nm) signals were monitored.
4493,10.1016/j.eurpolymj.2014.07.031,something_else,Dynamic light scattering (DLS) experiments were pe ... re added to 0.1 mg/ml ConA-FITC solution in water.
4494,10.1016/j.eurpolymj.2014.07.031,something_else,The samples for cryo transmission electron microsc ... mn energy filter set to 0-20 eV energy-loss range.
4495,10.1016/j.eurpolymj.2014.07.031,something_else,For fluorescence resonance transfer studies the pa ...  and allowed to react at room temperature for 2 h.
4496,10.1016/j.eurpolymj.2014.07.031,something_else,The amount of glucose on the nanoparticles were qu ... glucose solutions treated with the same procedure.
4497,10.1016/j.actbio.2015.02.030,something_else,"HTB4 cells were seeded into T75 plates, grown to c ... ne levels were expressed relative to basal levels."
4498,10.1016/j.eurpolymj.2014.07.031,something_else,The post-modification of PS-b-PFS aerosol nanopart ... ation of the dispersion was adjusted to 0.1 mg/ml.
4499,10.1016/j.eurpolymj.2014.07.031,something_else,PS-b-PFS and PS-b-PFS-GlcOH copolymer precursor so ... ls using a Berner-type low pressure impactor [31].
4500,10.1016/j.eurpolymj.2014.07.031,something_else,2.5 ml PS-b-PFS-GlcOH in DMF (2 mg/ml polymer conc ...  solution concentration was adjusted to 0.1 mg/ml.
4501,10.1016/j.eurpolymj.2014.07.031,something_else,The glucopyranose modification [6] and [30] of PS- ... fter drying in vacuum a yield of 63% was achieved.
4502,10.1016/j.eurpolymj.2014.07.031,something_else,The synthesis of the semifluorinated polystyrene-b ... nate (RITC) (Sigma-Aldrich) were used as received.
4503,10.1007/s10853-007-1837-x,something_else,"For microstructural examinations, specimens of the ... l walls from the magnified view of SEM micrograph."
4504,10.1007/s10853-007-1837-x,something_else,AA2014 Al-SiCp composites were synthesized using l ... ming 1.0 wt% CaH2 was added to the composite melt.
4505,10.1016/j.msea.2017.05.042,something_else,The initial material was a hot-rolled and mill-ann ... mmodated by twinning in α-Ti is less than 0.1 [9].
4506,10.1016/j.fuproc.2015.01.015,something_else,"However, when QDB-5-10 catalyst was used, the H2O/ ... %, with the hot spot temperature only at 317 degC."
4507,10.1016/j.eurpolymj.2014.07.031,something_else,"The glucose modified nanoparticles, PS-b-PFS-GlcOH ... ntration of 0.1 mg/ml, determined gravimetrically."
4508,10.1007/s40553-014-0008-7,something_else,"The SCTb, SCZY, and SZY films on the LPG fiber sur ... used in the SCTb, SCZY, and SZY film fabrications."
4509,10.1016/j.actbio.2015.02.030,something_else,"HTB4 cells were seeded into T75 plates, grown to c ... from 2 to 250 pg/ml with a sensitivity of 2 pg/ml."
4510,10.1016/j.actbio.2015.02.030,something_else,"HTB4 cells were grown to confluency on 8-well cham ...  with an Olympus IX81 (Olympus, Hamburg, Germany)."
4511,10.1016/j.ssc.2012.04.034,something_else,The graphene-MLG concentrations utilized for prepa ...  of samples with the carbon loading f~0.2-10 vol%.
4512,10.1016/j.ssc.2012.04.034,something_else,The surfactant stabilized graphene dispersion meth ... ate rc resulting in the largest η were determined.
4513,10.1016/j.jmoldx.2013.04.009,something_else,In-house MRSA PCR was performed using a 50x diluti ... nal from the S. aureus-specific genes nuc and coa.
4514,10.1016/j.jmoldx.2013.04.009,something_else,For coagulase and antimicrobial susceptibility tes ... performed following routine laboratory procedures.
4515,10.1016/j.jmoldx.2013.04.009,something_else,A total of 675 clinical isolates (of which >95% we ... ith 2.5% NaCl16 and incubated overnight at 35degC.
4516,10.1016/j.cattod.2006.05.011,something_else,Feed: CH4/O2/Ar = 2/1/45; catalyst: 15.0 mg; furna ...  degC; data were collected after 30 min on stream.
4517,10.1016/j.cattod.2006.05.011,something_else,The H2-TPR and O2-TPD experiments were performed b ... hermoStar quadrupole mass spectrometer (GSD301T2).
4518,10.1016/j.cattod.2006.05.011,something_else,The BET surface area of the catalyst was measured  ... ed down to 35 degC under vacuum for CO adsorption.
4519,10.1016/j.actbio.2015.02.030,something_else,HTB4 cells were seeded in 48-well plates and grown ...  standard disaccharides analysed in parallel runs.
4520,10.1016/j.cattod.2006.05.011,something_else,The pulsed reaction of CH4 was carried out at 600  ... s OmniStar quadrupole mass spectrometer (QMS 200).
4521,10.1016/j.cattod.2006.05.011,something_else,"The catalytic performance for POM to synthesis gas ...  m) for the separation of CH4, O2, H2, CO and CO2."
4522,10.1016/j.cattod.2006.05.011,something_else,Rh/Al2O3 catalysts were prepared by the wet impreg ... at 600 degC for 30 min before subjecting to tests.
4523,10.1016/j.jmatprotec.2007.06.021,something_else,Magnesium alloys were prepared using commercial AZ ... 0 mm x 25 mm and homogenized at 400 degC for 15 h.
4524,10.1016/j.actbio.2015.02.030,something_else,"All animal protocols were approved by the local an ... 40-60%, 4 = 60-80%, 5 80% staining) [47] and [48]."
4525,10.1016/j.actbio.2015.02.030,something_else,"HTB4 cells were seeded into corning transwell inse ... tham, MA) at 525 nm (FITC) and 625 nm (Rhodamine)."
4526,10.1016/j.actbio.2015.02.030,something_else,HTB4 cells were grown in 48-well plates until 90-1 ... mparison of 24-h closure versus time zero scratch.
4527,10.1016/j.actbio.2015.02.030,something_else,To examine the effect of HA on the expression of G ...  expression were determined using the ΔΔCT method.
4528,10.1016/j.actbio.2015.02.030,something_else,"HTB4 cells were grown until confluent on T25 flask ... ch, Arklow, Ireland) for live/dead identification."
4529,10.1016/j.cattod.2006.05.011,something_else,The TPSR experiments were performed by a Micromeri ... hermoStar quadrupole mass spectrometer (GSD301T2).
4530,10.1016/j.jcis.2015.06.014,something_else,"For PEC measurements, where specimens are required ... purity N2 (99.999%) prior to the PEC measurements."
4531,10.1016/j.cemconres.2016.06.009,something_else,Limestone filler with high fineness (Blaine approx ... content (but will also increase the Blaine value).
4532,10.1016/j.apcata.2007.06.015,something_else,Mono- and bimetallic catalysts were prepared by in ... Pt-Re/Al2O3 catalyst contained 0.3% of each metal.
4533,10.1016/j.tet.2007.06.061,something_else,"The product was synthesized according to the proce ... NOS2: C, 80.68; H, 5.27. Found: C, 80.59; H, 5.15."
4534,10.1016/j.tet.2007.06.061,something_else,"To 2-[N-,N-bis(9,9-dimethylfluorene-2-yl)phenyl]-t ... 3NOS: C, 83.78; H, 5.66. Found: C, 83.65; H, 5.52."
4535,10.1016/j.tet.2007.06.061,something_else,"For the preparation of DSSC, a washed FTO (Pilking ... red on an IPCE measuring system (PV measurements)."
4536,10.1016/j.tet.2007.06.061,something_else,All experiments were performed under a nitrogen at ... ccording to procedures reported in the literature.
4537,10.1016/j.tet.2007.06.061,something_else,"The novel organic dyes JK-5 and JK-6 were prepared ...  in acetonitrile, produced the JK-5 and JK-6 dyes."
4538,10.1016/j.electacta.2010.02.037,something_else,Two-electrode capacitors were assembled in a Swage ... n pure water equal to 82 mmol L-1 at 25 degC [18].
4539,10.1002/ejoc.201201363,something_else,"(2R*,3R*)-2-(Furyl-2-yl)-1,2,3,4-tetrahydro-3-(pro ... 30, H 7.16, N 5.85; found C 80.36, H 7.21, N 8.79."
4540,10.1002/ejoc.201201363,something_else,"(2R*,3R*)-2-(2,6-Dichlorophenyl)-1,2,3,4-tetrahydr ... 93, H 5.38, N 4.40; found C 67.87, H 5.35, N 4.48."
4541,10.1002/ejoc.201201363,something_else,"(2R*,3R*)-1,2,3,4-Tetrahydro-2-(3-nitrophenyl)-3-( ... 45, H 6.16, N 9.52; found C 73.56, H 6.22, N 9.47."
4542,10.1002/ejoc.201201363,something_else,"(2R*,3R*)-1,2,3,4-Tetrahydro-2-phenyl-3-(prop-1-en ... 70, H 7.68, N 5.62; found C 86.64, H 7.72, N 5.59."
4543,10.1002/ejoc.201201363,something_else,General Methods: All of the reagents were commerci ... ting points were measured in open capillary tubes.
4544,10.1007/s10008-007-0450-x,something_else,Electrochemical experiments were performed on elec ...  0.1 M Na2SO4 (at pH 1) as supporting electrolyte.
4545,10.1002/anie.200801638,something_else,Attempted Stille couplings between the iodoalkyne  ... isomerically pure pyrrhoxanthin (5) in 38 % yield.
4546,10.1002/anie.200801638,something_else,"Total synthesis of pyrrhoxanthin (5). a) 12, rac-1 ... LC instrument recorded for the eluate at λ=400 nm."
4547,10.1002/anie.200801638,something_else,"The ""dibromodiolefin"" rac-14 was prepared from bro ... hy on silica gel35 in 52 % yield (over two steps)."
4548,10.1002/anie.200801638,something_else,Syntheses of the bifunctional building blocks 13 a ... iisobutylaluminum hydride; NBS=N-bromosuccinimide.
4549,10.1002/anie.200801638,something_else,The synthesis of the heptatrienyldistannane 13 by  ... distannane 13 from the tetrolic ester 24 was 33 %.
4550,10.1016/j.tet.2007.06.061,something_else,"A mixture of 3 (0.41 g, 0.7 mmol), methyltriphenyl ... 5NOS: C, 84.14; H, 5.75. Found: C, 84.11; H, 5.69."
4551,10.1016/j.tet.2007.06.061,something_else,"The product was synthesized according to the proce ... NOS2: C, 81.11; H, 5.36. Found: C, 81.01; H, 5.29."
4552,10.1016/j.tet.2007.06.061,something_else,"The resulting acrylaldehyde thiophene (0.25 g, 0.4 ... 2O2S: C, 81.15; H, 5.33. Found: C, 80.88; H, 5.07."
4553,10.1016/j.tet.2007.06.061,something_else,"The resulting acrylaldehyde bithiophene (0.26 g, 0 ... O2S2: C, 78.71; H, 5.02. Found: C, 78.38; H, 4.91."
4554,10.1016/j.electacta.2007.02.063,something_else,The charge/discharge cycling tests were conducted  ... mperature throughout this study was about 25 degC.
4555,10.1016/j.cattod.2012.03.080,something_else,Model samples containing approximately the same am ... ature deN2O process is in the range 850-940 degC).
4556,10.1002/app.30995,something_else,"The solubility of PEIs 1c and 2c were the worst. P ... formamide (DMF), and N,N-dimethylacetamide (DMAc)."
4557,10.1002/app.30995,something_else,Infrared spectra were recorded on a Nexus-470 FTIR ... rded on a Hitachi U-3210 UV-vis spectrophotometer.
4558,10.1002/app.30995,something_else,PEI in powder form was obtained via chemical imidi ...  dried under vacuum at 120degC for 8 h before use.
4559,10.1002/app.30995,something_else,"PEI film was produced by imidization from PAA solu ...  2 h and 150, 200, 250, 300, and 350degC for 1 h)."
4560,10.1002/app.30995,something_else,"The PEIs were synthesized in two forms, i.e., film ... ature for 24 h to afford the soluble PAA solution."
4561,10.1002/app.30995,something_else,"The dianhydrides BPDA, ODPA, BTDA, and BPADA) were ... m Shanghai Research Institute of Synthetic Resins."
4562,10.1002/anie.200801638,something_else,Syntheses of the six-membered-ring reagents 10 and ... mide; MS=molecular sieves; NBS=N-bromosuccinimide.
4563,10.1002/app.30995,something_else,The diamines BAOFL and 6F-BAOFL were prepared as d ... e dried under vacuum at 80degC for 6 h before use.
4564,10.1002/asia.200900191,something_else,Depending on the direction of the flow of electron ... y's Law. The faradaic current is designated as IF.
4565,10.1002/asia.200900191,something_else,"In detailed studies, O'Mahony et al.63 have used t ... ive species employed in many voltammetric studies."
4566,10.1016/j.jeurceramsoc.2013.10.037,something_else,Schematic diagram of the experimental apparatus us ... phoretic deposition combined with ultrasonication.
4567,10.1016/j.jeurceramsoc.2013.10.037,something_else,"After binder burn-out, Si-infiltration was perform ...  in the skin, based on a preliminary test results."
4568,10.1016/j.jeurceramsoc.2013.10.037,something_else,EPD was performed for the cylindrical sample with  ...  performed at 350 degC for 2 h in a N2 atmosphere.
4569,10.1016/j.jeurceramsoc.2013.10.037,something_else,To prepare a slurry composed of β-SiC and carbon b ... sing 6 mm SiC balls to ensure particle dispersion.
4570,10.1016/j.jeurceramsoc.2013.10.037,something_else,After cutting the SiC fabrics into a rectangular s ...  an Ar atmosphere at a heating rate of 2 degC/min.
4571,10.1016/j.jeurceramsoc.2013.10.037,something_else,"A reticulated ERBISIC-R (Erbicol SA, Switzerland)  ... ure, Worldex, Korea) was used for Si-infiltration."
4572,10.1002/asia.200900191,something_else,"For voltammetry in organic solvents, it is common  ... "" behavior43 in ILs under voltammetric conditions."
4573,10.1016/j.apsusc.2005.12.017,something_else,The oligomer samples were ssDNA oligomers having t ...  then transferred to the STM chamber under vacuum.
4574,10.1016/j.electacta.2008.02.089,something_else,"The Sb modification on Pt electrode was carried ou ... y photoelectron spectroscopy (XPS, Multilab 2000)."
4575,10.1016/j.enconman.2006.03.008,something_else,The drying apparatus consisted of four sections: a ... yer was measured with the help of an energy meter.
4576,10.1016/j.enconman.2006.03.008,something_else,"The paddy (cultivar PR 116, medium size) used in t ... rther determined with the indirect moisture meter."
4577,10.1002/smll.201402757,something_else,"Surface Functionalization of Ag@Oxides Core-Shell  ... recipitate was redispersed in 1,2-dichlorobenzene."
4578,10.1002/smll.201402757,something_else,Synthesis of Ag@TiO2 Core-Shell Nanoprisms: Citric ... re repeated 3x to obtain clean Ag@TiO2 nanoprisms.
4579,10.1002/smll.201402757,something_else,"Chemicals: Poly(sodium styrene sulfonate) (PSSS, 2 ... cation system, and the resistivity was 18.2 MΩ cm."
4580,10.1007/s11663-013-9940-7,something_else,"During the industrial trials, copper platelets wer ... telets (1 to 3) and a fixed sampling location (P)."
4581,10.1007/s11581-015-1526-8,something_else,"For both the samples, applied anodization voltage  ... ormed using FESEM Hitachi, Japan model no. SU6600."
4582,10.1016/j.enconman.2006.03.008,something_else,The effect of the rest period drying conditions on ... ately 3/4th and above was considered as head rice.
4583,10.1007/s11581-015-1526-8,something_else,Fabrication of TiO2 nanotubes have been carried ou ... Alfa Aesar) and a counter electrode-platinum foil.
4584,10.1007/s10853-009-3432-9,something_else,Pure lead zirconate PbZrO3 and mixed PbZr1-xSnxO3  ... orm of cubes and rectangular prisms were obtained.
4585,10.1016/j.jpowsour.2015.03.139,something_else,Distribution of PbS (black) on four surfaces of do ...  to positive plate and (b) face to negative plate.
4586,10.1016/j.jpowsour.2015.03.139,something_else,In order to investigate the lead dendrite growth i ... he scan rate of 2deg min-1 with a step of 0.02deg.
4587,10.1016/j.jpowsour.2015.03.139,something_else,To understand the processes of H2SO4 diffusion and ... id in AGM separator to avoid the formation of H2S.
4588,10.1016/j.jpowsour.2015.03.139,something_else,The test batteries in this study were 6-DZM-12 VRL ... Na2SO4 at 20 degC and then placed in a water pool.
4589,10.1016/j.matlet.2007.12.035,something_else,Na-magadiite was synthesized according to the lite ... emplate of H-Magadiite in the 5.0 wt% HF solution.
4590,10.1007/s11144-010-0205-z,something_else,The precipitate was thoroughly washed in distilled ... ained from a precursor without a color transition.
4591,10.1007/s11144-010-0205-z,something_else,The activity test for the DME synthesis was carrie ... apak Q column and a thermal conductivity detector.
4592,10.1007/s10853-009-3432-9,something_else,The specific heat measurements were made using a N ... ere collected both on heating and cooling process.
4593,10.1007/s10853-016-0097-z,something_else,Graphene synthesis was performed on the catalytic  ... ctrometer with an excitation wavelength of 532 nm.
4594,10.1016/j.tsf.2014.12.012,something_else,"We used a typical hot-wall thermal CVD system (a h ... rious temperatures, gas ratios, and cooling rates."
4595,10.1007/s10800-010-0073-2,something_else,The cast iron anodes (4 cm x 4 cm) were mechanical ... ndard deviation for each system is also evaluated.
4596,10.1016/j.cemconres.2016.06.008,something_else,"A specimen of size 150 x 150 x 70 mm, equipped wit ...  The slump was 50 mm and the air content was 9.5%."
4597,10.1016/j.cemconres.2016.06.008,something_else,"When the freezing tests started, the specimens wer ... ent water depths were neglected in the test setup."
4598,10.1016/j.cemconres.2016.06.008,something_else,"The test setup was designed to simulate winter cli ...  specimens, the remaining surfaces were insulated."
4599,10.1016/j.cemconres.2016.06.008,something_else,The capillary absorption coefficient was determine ... ncreased by 40 to 160% compared to sound concrete.
4600,10.1016/j.cemconres.2016.06.008,something_else,The cubes were produced in the following manner. F ... ocedure was repeated until the moulds were filled.
4601,10.1016/j.cemconres.2016.06.008,something_else,"After splitting the cubes into two specimens, the  ... before being subjected to unidirectional freezing."
4602,10.1016/j.cemconres.2016.06.008,something_else,"After pre-mixing of cement and aggregate, water wa ... mperature of 20 degC and relative humidity of 65%."
4603,10.1016/j.biomaterials.2010.01.027,something_else,The biodegradation rate of PEA-AGs increased with  ... g/mL α-chymotrypsin solution) as shown in Fig. 10.
4604,10.1007/s10800-010-0073-2,something_else,To examine the role of starch in the phosphate rem ... he systems were maintained between 25 and 28 degC.
4605,10.1016/j.biomaterials.2010.01.027,something_else,"SEM was employed to analyze the surface morphology ...  scanning electron microscope (Mountain View, CA)."
4606,10.1016/j.biomaterials.2010.01.027,something_else,The solubility of the PEA-AGs (50 mg) in H2O and s ... oom temperature (25 degC) was evaluated (Table 3).
4607,10.1016/j.biomaterials.2010.01.027,something_else,Thermal properties of the synthesized polymers wer ... emperature (Tg) was taken at the inflection point.
4608,10.1016/j.biomaterials.2010.01.027,something_else,An example of the synthesis for the functionalized ... ally dried in vacuo at room temperature ( Fig. 5).
4609,10.1016/j.biomaterials.2010.01.027,something_else,"A detailed synthetic pathway of PEA-AG 8-Phe-4-AG- ... h, and finally dried in vacuo at room temperature."
4610,10.1016/j.biomaterials.2010.01.027,something_else,The synthetic procedure of monomer II were describ ... three times. The final products were white powder.
4611,10.1016/j.biomaterials.2010.01.027,something_else,"dl-2-Allylglycine (AG), l-Phenylalanine (Phe), p-t ...  and were purified by standard methods before use."
4612,10.1007/s10800-010-0073-2,something_else,"The available phosphate was estimated using the La ... using a UV-VIS spectrophotometer (Hitachi, Japan)."
4613,10.1007/s10800-010-0073-2,something_else,Iron formation and migration as a result of electr ... cess electrolyte collected at the cathode chamber.
4614,10.1016/j.biomaterials.2010.01.027,something_else,The biodegradation of the PEA-AGs was carried out  ... ilm sample on the basis of the following equation:
4615,10.1016/j.jssc.2008.04.036,something_else,All chemicals were used as received. 26.9 g of an  ... surfactant ratio) at 28 degC as listed in Table 1.
4616,10.1016/j.jssc.2008.04.036,something_else,"Catalytic activity of ceria nanoparticles was inve ... m3 (94 vol% helium, 6 vol% oxygen) up to 700 degC."
4617,10.1002/jhet.778,something_else,In a 50-mL round-bottom flask equipped with a magn ... ystallized from ethanol to get pure aurone (2a-f).
4618,10.1016/j.electacta.2011.08.087,something_else,"For chronoamperometry experiments, circular rotati ... g size, down to 1 μm and then rinsed with ethanol."
4619,10.1016/j.electacta.2011.08.087,something_else,Circular-shaped FTO (Fluorine Tin Oxide) substrate ... ts of ultra-pure water and dried under argon flow.
4620,10.1016/j.jpowsour.2016.02.068,something_else,Electrochemical measurements were performed using  ...  the galvanostatic measurements using the equation
4621,10.1016/j.jpowsour.2016.02.068,something_else,"KOH (0.5, 1, and 2 g) was added to an aqueous disp ... ansferred to a vacuum oven for storage at 30 degC."
4622,10.1016/j.jpowsour.2016.02.068,something_else,"Cotton cellulose powder (10 g, 20 μm, Sigma Aldric ... aqueous dispersions of CNCs was adjusted to 1 wt%."
4623,10.1016/j.fuproc.2015.01.018,something_else,A typical measurement run consisted of the followi ... averaged to ensure the reliability of the results.
4624,10.1016/j.fuproc.2015.01.018,something_else,A continuous gas stream of 2.9 l/min He/O2 is fed into the outer tube at 1000 degC.
4625,10.1016/j.canlet.2008.02.023,something_else,"Antibodies against ADAM17, p-EGFR, EGFR, p-Akt and ... tive cells or the positive area within each field."
4626,10.1016/j.electacta.2011.08.087,something_else,"Electrochemical measurements were carried out usin ... SCE, no deposit was possible below this potential."
4627,10.1016/j.canlet.2008.02.023,something_else,"Brain tissues isolated from PDT-treated or contral ... ng the Gelpro 4.5 program (Silver Spring, MD, US)."
4628,10.1016/j.canlet.2008.02.023,something_else,"U87 cells (ATCC, Manassas, VA, USA) were maintaine ...  PBS to a final concentration of 1 x 108 cells/ml."
4629,10.1016/j.canlet.2008.02.023,something_else,"Athymic nude mice were obtained from the National  ... mitted to sham surgery, with no exposure to light."
4630,10.1007/s10853-008-2867-8,something_else,A pin-on-disk tribometer was used to perform dry w ... e effect on friction coefficient of the composite.
4631,10.1007/s10853-008-2867-8,something_else,"For each specific condition, the test was repeated ... n, in order to calculate the volumetric wear rate."
4632,10.1016/j.optmat.2012.09.018,something_else,KGW particles calcined at 700 degC were used for d ... g. 1 shows the flow chart of texturing experiment.
4633,10.1002/app.29055,something_else,Monodispersed spherical particles (or micelles) wi ... DA) prepared in distilled water (shown in Fig. 8).
4634,10.1002/app.29055,something_else,The critical micelle concentration (CMC) was deter ...  polymer solution ranged from 1 x 10-6 to 1 mg/mL.
4635,10.1016/j.canlet.2008.02.023,something_else,"Athymic nude mice were anesthetized with ketamine  ... th 4-0 silk suture (Ethicon, Somerville, NJ, USA)."
4636,10.1002/app.29055,something_else,"The nanoparticle (or micelle) morphology was obser ... g method (Ion sputter coater HC-21, JEOL-108auto)."
4637,10.1016/j.electacta.2011.08.087,something_else,Electrochemical dedoping of 2 μm PPy/MoO42- electr ... Na2MoO4 aqueous solution at a scan rate of 5 mV/s.
4638,10.1002/macp.201200269,something_else,"Sebacic acid (Fluka), 1,8-octanediol (Sigma Aldric ... , --CH2OH), 4.27 (s, --CH2O--), 4.75 (t, --CH2OH)."
4639,10.1016/j.solmat.2009.01.014,something_else,fraction of incident energy transmitted after scat ... ittance due to Rayleigh scattering (dimensionless)
4640,10.1016/j.matlet.2014.12.030,something_else,"To synthesize micro-/nano-materials, the reducing  ... increased the volume to 4 or 5 mL (Fig. 2c and d)."
4641,10.1016/j.matlet.2011.06.009,something_else,The polymerization on the modified nano-SiO2 was c ... in the desiccator for future analysis experiments.
4642,10.1016/j.matlet.2011.06.009,something_else,"Tetraethoxysilane (TEOS, Guoyao Group of chemical  ... vents used in this study were of analytical grade."
4643,10.1016/j.matlet.2011.06.009,something_else,"In past decades, considerable efforts have been de ...  polymerization was initiated by thermo initiator."
4644,10.1002/pola.21165,something_else,Colored (ranging from light brown to black) polyhe ...  insoluble fractions in THF were obtained as well.
4645,10.1002/pola.21165,something_else,A typical procedure for oxidative polymerization i ... ter and methanol and dried under reduced pressure.
4646,10.1002/pola.21165,something_else,In a three-necked round-bottom flask equipped with ... ymers in THF and reprecipitating them in methanol.
4647,10.1002/macp.201200269,something_else,"Matrix-assisted laser desorption/ionization time-o ... vaporated, and a thin matrix/analyte film created."
4648,10.1002/pola.21165,something_else,A 20-mL three-necked round-bottom flask equipped i ... ing THF as eluent and reprecipitating in methanol.
4649,10.1002/pola.21165,something_else,"Certain amounts of monomer (CL), stannous octoate, ... t room temperature at reduced pressure for 3 days."
4650,10.1002/pola.21165,something_else,A round-bottom flask equipped with a magnetic stir ... ing THF as eluent and reprecipitating in methanol.
4651,10.1002/pola.21165,something_else,"Aminophenylboronic acid hemisulfate (Acros), 4-for ... um distilled over calcium hydride just before use."
4652,10.1002/macp.201200269,something_else,"SEC traces (THF) for the condensation polymerizati ...  10 min, t = 1 h, t = 6 h, t = 23 h, and t = 48 h."
4653,10.1002/macp.201200269,something_else,Since the monomer BHMO is an acid-sensitive oxetan ... cular-weight shoulder that could not be explained.
4654,10.1002/macp.201200269,something_else,"322 mg of BHMO and 12.6 mg of the photoinitiator I ...  period of time, an insoluble sample was obtained."
4655,10.1002/macp.201200269,something_else,The reaction was carried out in an NMR tube using  ... orded to analyze the shift of the end group peaks.
4656,10.1002/macp.201200269,something_else,"Novozyme 435 was dried in vacuum prior to use. The ... between 60% and 80%, depending on the composition."
4657,10.1002/pola.21165,something_else,A 100-mL three-necked round-bottom flask equipped  ... d the mixture was refluxed under nitrogen for 4 h.
4658,10.1002/app.29055,something_else,The particle size and the changes in the PolyAspAm ... aken after standing for 1 min at each temperature.
4659,10.1002/app.29055,something_else,The LCSTs of the polymer in a buffer solution (pH  ... ned as the temperature of 90% light transmittance.
4660,10.1016/j.jpcs.2009.07.010,something_else,All samples were prepared from pure elements (puri ...  800 degC for at least 30 min and then air cooled.
4661,10.1016/j.jssc.2011.01.015,something_else,"Calcinations in stagnant air, ZnO single-phase rem ...  formed randomly in the ZHC sample by water vapor."
4662,10.1016/j.jssc.2011.01.015,something_else,"It is noteworthy that in stagnant air, the residua ... ) corresponds to the formation of 4.77 mol of ZnO."
4663,10.1016/j.jssc.2011.01.015,something_else,"As shown in Fig. 3, up to 230 degC, ZHC is decompo ...  chlorine are not released by heating to 230 degC."
4664,10.1016/j.jssc.2011.01.015,something_else,"In contrast, the cooling process in dry N2 showed  ... t regeneration of β-Zn(OH)Cl and ZHC was promoted."
4665,10.1016/j.jssc.2011.01.015,something_else,In order to clarify the influence of water vapor o ... to the furnace preheated to a desired temperature.
4666,10.1016/j.bbamcr.2013.02.014,something_else,Cells were lysed in RIPA lysis buffer (50 mM Tris- ... he corresponding protein in untreated cells (Co.).
4667,10.1016/j.bbamcr.2013.02.014,something_else,"RNA was isolated from cultured cells using Zymo Re ... tion, expression of control was equivalent to one."
4668,10.1007/s10853-014-8603-7,something_else,Mesoporous silica (SiO2) was obtained by molecular ...  solid was filtered and dried at 45 degC for 24 h.
4669,10.1016/j.bbamcr.2013.02.014,something_else,"To examine the intracellular localization of cytoc ... microscope (Leica Microsystems, Nanterre, France)."
4670,10.1016/j.bbamcr.2013.02.014,something_else,"For flow cytometry analysis of mitochondrial trans ... L cytometer (Beckman Coulter, Villepinte, France)."
4671,10.1016/j.bbamcr.2013.02.014,something_else,Human HeLa cervical cancer cells stably transfecte ... All other fluorescent probes were from Invitrogen.
4672,10.1016/j.tetlet.2012.11.061,something_else,Then aldehyde 5 was subjected to Still's modified  ... n good agreement with the natural product. 7 and 8
4673,10.1016/j.tetlet.2012.11.061,something_else,"Reagents and conditions: (a) vinylmegnesium bromid ...  (e) AD Mix-α,t-BuOH:H2O (1:1), 0 degC, 24 h, 86%."
4674,10.1016/j.tetlet.2012.11.061,something_else,The synthesis of botryolide-E (1) is based on a se ...  reaction without further purification (Scheme 2).
4675,10.1016/j.tetlet.2012.11.061,something_else,"Recently, many groups have synthesized this molecu ... l), and Klebsiella pneumonia (MTCC 39) (50 μg/ml)."
4676,10.1002/jhet.778,something_else,"The antimicrobial activity was assayed in vitro by ... egC for 24 h and at 30degC for 48 h, respectively."
4677,10.1002/jhet.778,something_else,In a 100-mL three-necked round-bottom flask equipp ... pounds were recrystallized from chloroform-hexane.
4678,10.1016/j.bbamcr.2013.02.014,something_else,"Cells were fixed with 2% glutaraldehyde/0.1 M sodi ... croscopy facility of INRA (Jouy-en-Josas, France)."
4679,10.1002/app.29055,something_else,The pKa value of the polymer was measured using th ... ith 0.1N HCl in a given volume increment (100 μL).
4680,10.1007/s10853-014-8603-7,something_else,The hybrid mesoporous silicas were obtained throug ... resulting solid was filtered and dried at 70 degC.
4681,10.1007/s10853-014-8603-7,something_else,The cyanide solution from the Pena de Bernal ore ( ... vered solution was used in the adsorption studies.
4682,10.1002/app.29055,something_else,"PSI was prepared and purified according to a previ ... 0.8-0.76 (br, 3H, NHCH2CH2(CH2)mCH3) (see Fig. 1)."
4683,10.1002/app.29055,something_else,"L-Aspartic acid (98+%), O-phosphoric acid (98%), N ... f high quality and were used without purification."
4684,10.1016/j.immuni.2012.12.003,something_else,"For cell-cycle analysis, cells were incubated with ... rMingen) according to the manufacturer's protocol."
4685,10.1016/j.immuni.2012.12.003,something_else,Bone marrow LSK cells were cultured in DMEM medium ... nd IL-33. Cytokines were purchased from Peprotech.
4686,10.1016/j.immuni.2012.12.003,something_else,All antibodies (Abs) used were purchased from eBio ... ces) according to the manufacturer's instructions.
4687,10.1016/j.immuni.2012.12.003,something_else,Mice were exsanguinated and lungs were perfused by ... cs). Cells were filtered by using a cell strainer.
4688,10.1016/j.immuni.2012.12.003,something_else,C57BL/6 (CD45.2) and B6-Ly5.2 (CD45.1) mice were p ... mittee policies at the University of Pennsylvania.
4689,10.1016/j.immuni.2012.12.003,something_else,(C) An equal number of ILC2 that were derived from ... iments; three mice per group (error bars are SEM).
4690,10.1007/s10853-014-8603-7,something_else,"A standard solution of 2000 mg L-1 of Cu(I)-CN was ... of Cu, which were used for the adsorption studies."
4691,10.1016/j.matdes.2015.08.009,something_else,Frames for the 1st and 2nd stages of testing were  ... ere allowed to cure at least 1 day before testing.
4692,10.1002/cvde.201207051,something_else,"Pure ZnO and Al2O3 films were deposited in a comme ... gy were examined by AFM (Cypher, Asylum Research)."
4693,10.1002/cvde.201207051,something_else,"Al-doped ZnO (AZO) films are deposited at 200degC  ... 9.4 x 10-4 Ω cm, with better optical transparency."
4694,10.1016/j.cej.2007.11.019,something_else,The ozonation process started when the ozone-oxyge ... s were measured before and after 30 min ozonation.
4695,10.1016/j.cej.2007.11.019,something_else,The aqueous dye solution was prepared by dissolvin ... nd in residual dyebaths and diluted effluents [6].
4696,10.1016/j.cej.2007.11.019,something_else,Ozone was generated from pure oxygen by a Model GL ... ore details were described elsewhere [6] and [10].
4697,10.1016/j.cej.2007.11.019,something_else,"C.I. Reactive Blue 15 was purchased from Sigma-Ald ... all supplied by VWR Canlab (Mississauga, Ontario)."
4698,10.1007/s10853-014-8603-7,something_else,"On the other hand, the Cu(I) removed with SiO2-Ph  ... rption spectrophotometer Perkin Elmer Analyst-200."
4699,10.1007/s10853-014-8603-7,something_else,The Cu(I) removal by the mesoporous and hybrid sil ... r Analyst-200 at a lapse of 15 min during 140 min.
4700,10.1016/j.matdes.2015.08.009,something_else,Frames with dowel nut and bed bolt joints were con ... ured 6.4 mm in diameter by 38.1 mm long (Fig. 1c).
4701,10.1007/s11144-010-0205-z,something_else,"The Cu-Zn-Al catalyst is conventionally prepared f ... compositions of the Cu-Zn-Al-hydrotalcites [8, 9]."
4702,10.1007/s11144-010-0205-z,something_else,"A series of methanol synthesis catalysts, CuO/ZnO/ ... rsor, hydrotalcite-like layered double hydroxides."
4703,10.1002/j.1939-4640.2004.tb03175.x,something_else,Testicular interstitial fluid (IF) was collected a ... ass). The sensitivity of the assay was 10 pg/tube.
4704,10.1016/j.tetlet.2012.03.091,something_else,General experimental procedure: To a clean dry 10  ... 2*4H2O for 13 h at 145 degC by reported procedure.
4705,10.1016/j.tetlet.2012.03.091,something_else,A further set of experiment was carried out to che ... 00% selectivity in favor of benzophenone (Fig. 2).
4706,10.1016/j.tetlet.2012.03.091,something_else,The oxidation of DPM was also carried out with dif ... urther oxidation of benzhydrol gives benzophenone.
4707,10.1016/j.jpowsour.2016.02.061,something_else,Electrochemical experiments were performed on a CR ... 1.8-2.8 V using the same potentiostat-galvanostat.
4708,10.1016/j.jpowsour.2016.02.061,something_else,The olive stone activated carbon was obtained at t ...  in a tubular furnace under a nitrogen atmosphere.
4709,10.1016/j.jorganchem.2012.03.031,something_else,Coulometry for bulk electrolysis at -2.40 V vs. Fc ... r is referred to the web version of this article.)
4710,10.1016/j.jeurceramsoc.2017.01.009,something_else,Two blocks of different compositions were prepared ... d borosilicate glass for the other (ZB hereafter).
4711,10.1016/j.jeurceramsoc.2017.01.009,something_else,Electro-fusion and casting is used to produce larg ... ues in the interior of the block were encountered.
4712,10.1016/j.matdes.2015.08.008,something_else,The rolled samples were subjected to a recrystalli ... pecimen used for this study is shown in Fig. 1(b).
4713,10.1002/anie.200801636,something_else,"[a] Reactions were carried out with 1 b-e (0.5 mmo ... ol), and I (10 mol %) in MTBE (15 mL) at -20 degC."
4714,10.1016/j.cattod.2006.05.010,something_else,The Au/CeO2 model structure was also prepared by v ... maging Filter. The spectra were obtained in 2-4 s.
4715,10.1016/j.jmatprotec.2007.06.026,something_else,The experiments have been conducted in six set-ups ... as measured for finding difference in weight loss.
4716,10.1002/chem.200701570,something_else,Characterization: The UV/Vis spectra were recorded ...  into a vial and diluted with iso-propanol (5 mL).
4717,10.1002/chem.200701570,something_else,Synthesis of Au nanoparticles from AuCl and AuBr:  ...  with octadecylamine followed the same procedures.
4718,10.1002/chem.200701570,something_else,"Chemicals: All solvents, including chloroform, hex ... rom Aldrich and used without further purification."
4719,10.1002/chem.200701570,something_else,The first synthesis of Au colloids was reported [? ... een extended to the synthesis of Au nanoparticles.
4720,10.1016/j.matlet.2007.03.041,something_else,All the reagents and chemicals of AR grade were us ... rd deflection of the curve peak from the baseline.
4721,10.1002/anie.200801636,something_else,"[a] Unless otherwise indicated, reactions were car ... H). [g] From ref. 5 (with 10 equivalents of MeOH)."
4722,10.1016/j.jeurceramsoc.2010.12.008,something_else,"After the reference sample, the LTCC packaged vers ... nsisted of 30 LTCC layers, as presented in Fig. 2."
4723,10.1016/j.jmbbm.2012.02.016,something_else,All block copolymer samples were compression molde ... nd stored in a desiccator before characterization.
4724,10.1002/ejoc.200600230,something_else,General Procedure for the Synthesis of Butadienylb ...  which was then purified by column chromatography.
4725,10.1016/j.polymdegradstab.2015.09.009,something_else,"Results of the experiment into the dosage of chito ... eaction temperature, 180 degC; reaction time, 5 h."
4726,10.1016/j.polymdegradstab.2015.09.009,something_else,"Effect of reaction time on 5-HMF production. React ... s solution, 4 wt%; reaction temperature, 180 degC."
4727,10.1016/j.polymdegradstab.2015.09.009,something_else,"Effect of reaction temperature on 5-HMF production ... iquid aqueous solution, 4 wt%; reaction time, 5 h."
4728,10.1016/j.polymdegradstab.2015.09.009,something_else,"Effect of different concentration of ionic liquid  ... 00 mg; distilled water, 20 mL; reaction time, 5 h."
4729,10.1016/j.polymdegradstab.2015.09.009,something_else,The yield of 5-HMF was affected by different conce ... entration of [MIM]HSO4 improve the yield of 5-HMF.
4730,10.1016/j.polymdegradstab.2015.09.009,something_else,The experiment were refluxed in 50 mL round-bottom flask at 180 degC in the oil bath.
4731,10.1016/j.polymdegradstab.2015.09.009,something_else,"Experiment conditions: chitosan, 100 mg; distilled ... lution, 2 wt%; temperature, 150 degC and 180 degC."
4732,10.1016/j.polymdegradstab.2015.09.009,something_else,"After the reaction completion, the solid residue w ... istilled water under the same reaction conditions."
4733,10.1002/ejoc.200600230,something_else,General Remarks: Flasks and all equipment used for ... y column (25 m x 0.2 mm x 0.33 μm film thickness).
4734,10.1016/j.polymdegradstab.2015.09.009,something_else,The structures of chitosan and the solid residue w ... ared by mixing with KBr and compacting into discs.
4735,10.1016/j.polymdegradstab.2015.09.009,something_else,"The qualitative analysis of 5-HMF (Fig. 1) was con ... a scan range of m/z 50-500, at a rate of 1 scan/s."
4736,10.1002/ejoc.200600230,something_else,"4-Ethoxy-2,2-dimethyl-2H-chromene (6b): (0.075 g,  ... 6): calcd. C 76.44, H 7.90; found C 76.99; H,7.45."
4737,10.1002/ejoc.200600230,something_else,"General Procedure for the Synthesis of Chromenes 6 ... n neutral Al2O3 (light petroleum ether/Et2O, 9:1)."
4738,10.1002/ejoc.200600230,something_else,"Typical Procedure for the Synthesis of 2,3-Dihydro ... 63, H 5.81, N 4.25; found C 66.20, H 5.05, N 4.80."
4739,10.1002/ejoc.200600230,something_else,"Typical Procedure for the Synthesis of 4-Ethoxy-1, ... 20, H 6.49, N 3.92; found C 68.05, H 5.99, N 4.08."
4740,10.1002/ejoc.200600230,something_else,"4-Ethoxy-2,3-dimethylquinoline (4c): The crude rea ... 58, H 7.51, N 6.96; found C 76.20, H 8.01, N 6.02."
4741,10.1002/ejoc.200600230,something_else,"General Procedure for the Synthesis of Quinolines  ... iO2 (Et3N, 1 %, light petroleum ether/EtOAc, 6:1)."
4742,10.1002/ejoc.200600230,something_else,"General Procedure for the Synthesis of Dienylbenze ... SiO2 (Et3N, 1 %; light petroleum ether/Et2O, 9:1)."
4743,10.1016/j.polymdegradstab.2015.09.009,something_else,The amount of TRS in the product sample was measur ... nd yield (YTRS) of TRS were calculated as follows:
4744,10.1016/j.polymdegradstab.2015.09.009,something_else,"Results of the experiment into the water volume fo ... eaction temperature, 180 degC; reaction time, 5 h."
4745,10.1016/j.jeurceramsoc.2010.12.008,something_else,Two different samples were manufactured using the  ... lock sintering profile provided by the supplier.13
4746,10.1016/j.poly.2015.01.007,something_else,"Sodium boranocarbonate (4.4 mg, 0.054 mol), disodi ...  synthesis (Rt = 17.95 min). HPLC: Rt = 18.22 min."
4747,10.1016/j.cattod.2012.02.039,something_else,Two commercial TiO2 (Aldrich) sample were used: an ... alysts will be denoted as Rh/TiO2-A and Rh/TiO2-R.
4748,10.1016/j.electacta.2010.02.035,something_else,A potentiostat PARSTAT2273 comprised of a conventi ... alomel electrode (SCE) as the reference electrode.
4749,10.1016/j.electacta.2010.02.035,something_else,The specimens acting as working electrodes were em ... rom analytical grade reagents and distilled water.
4750,10.1016/j.electacta.2010.02.035,something_else,"The investigated material was a commercial standar ...  atmosphere, for 1 h, followed by water quenching."
4751,10.1111/j.1551-2916.2007.01904.x,something_else,"Particle size was determined from surface area mea ... icroscope (SEM) (S-3500N, Hitachi, Berkshire, UK)."
4752,10.1016/j.cemconres.2009.12.001,something_else,Tests are performed on normal consistency cement p ... xing and on different samples from the same batch.
4753,10.1016/j.materresbull.2011.12.020,something_else,"The oxygen permeation flux JO2 (ml/cm2 min) throug ...  area, the flux JO2 is given by the relation [47]:"
4754,10.1016/j.jcis.2013.10.059,something_else,GO-ZnO and rGO-ZnO compositions were fabricated by ... g power of 100 W used during sputtering for 1.5 h.
4755,10.1016/j.cattod.2012.02.039,something_else,"The gaseous feed was composed of a mixture of 5 vo ... x, Hayesep Q CP81069, Molsieve 5A and CP-sil 5CB)."
4756,10.1016/j.jcis.2013.10.059,something_else,"Natural graphite (99.9%) powders are commercially  ... h Institute for Nonferrous Metals, Beijing, China."
4757,10.1002/app.24115,something_else,The polymer solution was prepared by dissolving th ... ion of the polymer occurred without ascorbic acid.
4758,10.1002/app.24115,something_else,"Poly(ethylene oxide) was obtained from Sigma Aldri ... id (S.D. Fine chemicals, India) was of 99% purity."
4759,10.1016/j.apcata.2007.06.015,something_else,Hydrogen (a) and oxygen (b) adsorption on Pt-Re/Al ... nes correspond to H/Pt = 1 (a) and O/Pt = 0.7 (b).
4760,10.1016/j.apcata.2007.06.015,something_else,XANES Re LIII spectra: (1) Pt-Re/Al2O3 oxidized at ... gC in Ar and reduced at 500 degC; (4) metallic Re.
4761,10.1016/j.apcata.2007.06.015,something_else,Temperature-programmed reduction of Pt-Re/Al2O3 pr ...  100 degC in air; (2) calcined at 500 degC in air.
4762,10.1016/j.apcata.2007.06.015,something_else,Temperature-programmed reduction (TPR) was perform ... cination in air either at 100 degC or at 500 degC.
4763,10.1016/j.apcata.2007.06.015,something_else,"To study the metal segregation over Pt-Re/Al2O3, t ... cuated at 500 degC before adsorption measurements."
4764,10.1016/j.apcata.2007.06.015,something_else,Hydrogen and oxygen chemisorption over mono- and b ... r oxygen molecules chemisorbed on metal particles.
4765,10.1002/app.24115,something_else,"The molecular weight distribution was monitored by ... EO and PAM were 850,000 and 321,000, respectively."
4766,10.1016/j.msea.2012.01.042,something_else,Grain orientations were determined using a LEO 153 ... d <1 1 1>-orientations for micro pillar machining.
4767,10.1002/polb.20969,something_else,"The biodegradable polymer, poly(lactic acid) (PLA) ... electrodes of 5 mm and were supplied by ICM (USA)."
4768,10.1016/j.matlet.2014.12.037,something_else,"Co-precipitation is a more tractable and efficient ... d after collecting, rinsing, filtering and drying."
4769,10.1016/j.poly.2015.01.007,something_else,"fac-[NEt4]2[Re(CO)3(Br)3] (30.0 mg, 0.039 mmol) wa ... 3.97; N, 4.24. Found: C, 34.59; H, 4.05; N, 4.29%."
4770,10.1016/j.poly.2015.01.007,something_else,"1 ml of a 2 x 10-3 M 1-methyl-2-thiourea methanol  ... 1.91; N, 7.98. Found: C, 27.31; H, 1.93; N, 8.02%."
4771,10.1016/j.poly.2015.01.007,something_else,"1 ml of a 2 x 10-3 M thiourea methanol solution an ... 1.57; N, 8.20. Found: C, 25.71; H, 1.61, N, 8.16%."
4772,10.1016/j.poly.2015.01.007,something_else,"1 ml of a 2 x 10-3 M tetraethylammonium thiocyanat ... 3.87; N, 6.73. Found: C, 36.45; H, 3.81; N, 6.71%."
4773,10.1016/j.poly.2015.01.007,something_else,"1 ml of a 2 x 10-3 M imidazole in methanol solutio ... 1.40; N, 8.35. Found: C, 31.05; H, 1.49; N, 8.31%."
4774,10.1016/j.poly.2015.01.007,something_else,"1 ml of a 2 x 10-3 M pyridine solution in methanol ... 1.76; N, 5.43. Found: C, 34.89; H, 1.81, N, 5.38%."
4775,10.1016/j.poly.2015.01.007,something_else,"1 ml of a 2 x 10-3 M tetraethylammonium iodide met ... 3.49; N, 4.04. Found: C, 31.08; H, 3.54; N, 4.08%."
4776,10.1016/j.poly.2015.01.007,something_else,"fac-[Re(2,5-PicoH)(CO)3(H2O)] (46.0 mg, 0.1 mmol)  ... 1.72; N, 2.99. Found: C, 28.28; H, 1.69; N, 2.92%."
4777,10.1002/polb.20969,something_else,"The 9 MHz crystals were thoroughly cleaned with di ... fore coating and after the thermal treatment, ΔFC."
4778,10.1016/j.poly.2015.01.007,something_else,"fac-[NEt4]2[Re(CO)3(Br)3] (100.0 mg, 0.130 mmol) w ... 1.33; N, 3.08. Found: C, 26.45; H, 1.30; N, 3.12%."
4779,10.1016/j.poly.2015.01.007,something_else,"The infrared spectra were recorded as KBr pellets  ... ppm, 30.83 ppm) peak for 1H and 13C, respectively."
4780,10.1016/j.poly.2015.01.007,something_else,Rhenium pentacarbonyl bromide was purchased from S ... s. All the experiments were performed aerobically.
4781,10.1016/j.electacta.2007.02.028,something_else,Pseudo catalyst test samples were prepared by puls ... ied pulses were 0 mV (100 ms) and 1500 mV (10 ms).
4782,10.1016/j.electacta.2007.02.028,something_else,The SECM instrument has been described previously  ... ode. A Pt-foil (1 cm) served as counter electrode.
4783,10.1016/j.conbuildmat.2005.06.042,something_else,The double lap joints were made using two CFRP str ... geometry of specimen J1 is illustrated in Fig. 14.
4784,10.1016/j.conbuildmat.2005.06.042,something_else,The same bonding technique was used for the two di ...  and 0.8 mm for specimen bonded by Sikadur(r) 330.
4785,10.1016/j.conbuildmat.2005.06.042,something_else,"Hot rolled steel bars were used to fabricate the s ... of 317.8 and 433 MPa, respectively, were obtained."
4786,10.1016/j.conbuildmat.2005.06.042,something_else,A two component epoxy resin Sikadur(r) 30 was used ...  life of 30 min and was cured at room temperature.
4787,10.1016/j.poly.2015.01.007,something_else,"fac-[NEt4]2[Re(CO)3(Br)3] (100.0 mg, 0.130 mmol) w ... 3.94; N, 4.22. Found: C, 32.40; H, 3.85; N, 4.21%."
4788,10.1016/j.polymdegradstab.2015.09.009,something_else,"Experiment conditions: chitosan, 100 mg; distilled ... 4) aqueous solution, 4 wt%; temperature, 180 degC."
4789,10.1016/j.polymdegradstab.2015.09.009,something_else,Efficient conversion of cellulose into biofuel pre ... rfural in dimethyl sulfoxide-ionic liquid mixtures
4790,10.1016/j.biomaterials.2013.11.039,something_else,"A predetermined amount of miR-21i (20 μm/L) was ad ...  a gel doc system (G:BOX Chemi XR5, Syngene, USA)."
4791,10.1016/j.biomaterials.2013.11.039,something_else,"Next, 4 mg of DOX-loaded micelles (D-sCPM1, D-sCPM ...  the release amount of the drugs to be calculated."
4792,10.1016/j.biomaterials.2013.11.039,something_else,pEGFP plasmid was used to study the gene transfect ... ene was counted under the fluorescence microscope.
4793,10.1016/j.biomaterials.2013.11.039,something_else,The cytotoxicity of three sCPM was evaluated by th ... gth of 570 nm using a spectrophotometric analysis.
4794,10.1016/j.biomaterials.2013.11.039,something_else,"The micelles of PLA-PDMAEMA3, (PLA-PDMAEMA3)2, and ...  stirred for 8 h to evaporate the dichloromethane."
4795,10.1016/j.biomaterials.2013.11.039,something_else,The critical micelle concentration (CMC) was deter ... e copolymer concentration was used to measure CMC.
4796,10.1016/j.biomaterials.2013.11.039,something_else,"For the click coupling reaction, 1.0 g (0.051 mmol ... os of the PLA proton peak and PDMAEMA proton peak."
4797,10.1016/j.biomaterials.2013.11.039,something_else,"Choosing (PLA-PDMAEMA3)3 as an example (Scheme 2), ... The Mw and PDI of sPLA-(N3)3 were measured by GPC."
4798,10.1016/j.biomaterials.2013.11.039,something_else,"D-sCPM1/FITC-miR-21i, D-sCPM2/FITC-miR-21i and D-s ... etected by flow cytometry (Becton Dickinson, USA)."
4799,10.1016/j.biomaterials.2013.11.039,something_else,"Initiator BOBiB (83 mg, 0.38 mmol) was dissolved i ... s the eluant at a flow rate of 1 mL/min (30 degC)."
4800,10.1016/j.biomaterials.2013.11.039,something_else,"First, 6.0 g of lactide were added to a reaction t ... Cl3 with a Varian 500 MHz spectrometer instrument."
4801,10.1016/j.biomaterials.2013.11.039,something_else,"3-Bromo-2,2-bis(bromomethyl) propanol (5.0 g,15.4  ... USA) (Supplementary information, Figs. S1 and S2)."
4802,10.1016/j.biomaterials.2013.11.039,something_else,"3-Butyn-1-ol, 2-bromo isobutyryl bromide, CuBr, so ... pyrocarbonate (DEPC) water and frozen at -20 degC."
4803,10.1016/j.apenergy.2008.01.001,something_else,"The 12 appliances are refrigerator, freezer, micro ... r of appliances that any household can have is 11."
4804,10.1016/j.apcata.2007.04.007,something_else,A 1 M solution of BH3*THF (0.25 mmol) was added at ... d be recycled after washing with water and drying.
4805,10.1016/j.apcata.2007.04.007,something_else,A solution of m-clorosolfophenyl phosphonic acid [ ... white solid and used without further purification.
4806,10.1016/j.apcata.2007.04.007,something_else,Sample 1 warmed at 100 degC and BH3*THF were used  ... ntiomeric excess obtained are reported in Table 3.
4807,10.1016/j.apcata.2007.04.007,something_else,Several samples of α-Zirconium-N-(m-solfophenyl)-l ... -Valine-Phosphonic acid and Methanphosphonic acid.
4808,10.1016/j.biomaterials.2013.11.039,something_else,"To begin, 1.0 mL (13.2 mmol) of 3-Butyn-1-ol and 1 ... ed by 1H NMR (Supplementary information, Fig. S3)."
4809,10.1016/j.apcata.2007.04.007,something_else,"Several α-Zr[O3PC6H4SO2NHCH(CH(CH3)2)COOH)]2-x(O3P ... THF at 0 degC, with enantiomeric excess up to 50%."
4810,10.1016/j.biomaterials.2013.11.039,something_else,Confocal fluorescent microscopy was used to assess ... ) with identical settings for each confocal study.
4811,10.1016/j.biomaterials.2013.11.039,something_else,The glioma cells LN229 were treated with various g ... used according to the manufacturer's instructions.
4812,10.1002/j.1939-4640.2004.tb03175.x,something_else,"RNA was purified from isolated Sertoli, germ, and  ... led RNA from the isolated Sertoli cells of 2 rats."
4813,10.1002/j.1939-4640.2004.tb03175.x,something_else,Membranes were blocked for 1 hour with 5% nonfat d ... erformed 3 times with 3 different sets of samples.
4814,10.1002/j.1939-4640.2004.tb03175.x,something_else,Proteins were isolated from soluble and insoluble  ... f) according to the manufacturer's specifications.
4815,10.1002/j.1939-4640.2004.tb03175.x,something_else,Detergent-soluble G-actin monomeric proteins from  ... nhibitor cocktail [Sigma]) by means of sonication.
4816,10.1002/j.1939-4640.2004.tb03175.x,something_else,Sertoli cells freshly isolated from control or hyp ... c camera system with a 60x oil Zeiss PlanApo lens.
4817,10.1002/j.1939-4640.2004.tb03175.x,something_else,Leydig cells were isolated from untreated rats by  ...  blood cells making up the principal contaminants.
4818,10.1002/j.1939-4640.2004.tb03175.x,something_else,Total testicular germ cells were isolated by incub ... Sertoli cells making up the principal contaminant.
4819,10.1002/j.1939-4640.2004.tb03175.x,something_else,Sertoli cells were isolated according to previousl ... ty. Germ and myoid cells made up the contaminants.
4820,10.1016/j.biomaterials.2013.11.039,something_else,A colony formation assay was used to measure the p ...  for 1 min. Each group was measured in triplicate.
4821,10.1002/j.1939-4640.2004.tb03175.x,something_else,Hypophysectomized and untreated Sprague-Dawley rat ...  Hopkins University Animal Care and Use Committee.
4822,10.1016/j.watres.2011.08.021,something_else,"The group of Aeromonas spp. isolates comprised 80  ... he WTP, including in tap water ( Table 2, Fig. 1)."
4823,10.1007/s10800-009-9968-1,something_else,The specific SnO2/Ir/Ti prepared by metal-organic  ... ctrodes service life measurement is still running.
4824,10.1007/s10800-009-9968-1,something_else,The electrochemical characterization was performed ... TOC was determined by Shimadzu TOC-5050A analyzer.
4825,10.1016/j.biomaterials.2013.11.039,something_else,"Tianjin Research Center of Basic Medical Science, Tianjin Medical University, Tianjin 300070, China"
4826,10.1016/j.biomaterials.2013.11.039,something_else,"The paraffin-embedded tissue sections were used fo ... atoxylin, and visualized using a light microscope."
4827,10.1016/j.biomaterials.2013.11.039,something_else,"BALB/c-A nude mice, four to six weeks old, were pu ... red using the formula: volume = length x width2/2."
4828,10.1016/j.biomaterials.2013.11.039,something_else,"Glioma cells were treated with different groups as ... gnal protein detection kit (Pierce, Rockford, IL)."
4829,10.1016/j.biomaterials.2013.11.039,something_else,"Apoptosis was evaluated by flow cytometry analysis ... S flow cytometer (Becton Dickinson, San Jose, CA)."
4830,10.1016/j.watres.2011.08.021,something_else,"No aeromonads were isolated from ground water or f ... ater chlorination, including in 11 household taps."
4831,10.1016/j.polymdegradstab.2015.09.009,something_else,"Recycle of [MIM]HSO4 for the transformation of chi ... eaction temperature, 180 degC; reaction time, 5 h."
4832,10.1016/j.jssc.2008.04.035,something_else,The photodegradation of acid red G aqueous solutio ... an be represented empirically by the equation [24]
4833,10.1002/anie.201510331,something_else,By replacing the commonly used ethyl acetate for s ... n of VD3 (1) into preVD3 (5) is not rate limiting.
4834,10.1016/j.chemosphere.2014.04.065,something_else,The frozen lung and trachea tissue samples were th ... ls. cDNA product was stored at -80 degC until use.
4835,10.1016/j.chemosphere.2014.04.065,something_else,"Under anesthesia, the blood samples were obtained  ... trogen for total RNA and total protein extraction."
4836,10.1016/j.chemosphere.2014.04.065,something_else,"Male Wistar rats, weighing 180-200 g, were purchas ... , 2006). Sham immunizations were done with saline."
4837,10.1016/j.cplett.2003.10.121,something_else,Glasses were prepared by melt-quenching technique. ... ned are transparent and have good optical quality.
4838,10.1007/s40940-016-0025-2,something_else,A light optical microscope with double magnificati ... ding rollers of the four point bending test-setup.
4839,10.1016/j.jlumin.2014.06.006,something_else,"Bulk crystalline samples of Er:CLNGG, of concentra ...  the congruent formula Ca3Li0.275Nb1.775Ga2.95O12."
4840,10.1016/j.jeurceramsoc.2013.10.030,something_else,"The XRD-diffractogramms of LiCoPO4 powders, prepar ... ical performance of LiCoPO4 is still under debate."
4841,10.1016/j.jeurceramsoc.2013.10.030,something_else,"The structural analysis, SEM imaging and electroch ... surements have been performed at room temperature."
4842,10.1016/j.chemosphere.2014.04.065,something_else,"Cellular plasma and nuclear protein were extracted ... Infrared Imaging System (Li-COR Biosciences, USA)."
4843,10.1016/j.apsusc.2005.12.016,something_else,SEM picture of ordered array of columns (right) an ... the magnetic field of 0.2 T on Si/Si3N4 substrate.
4844,10.1016/j.apsusc.2005.12.016,something_else,Spherical cobalt nanoparticles (NPs) were prepared ... s and GISAXS studies is 5.7 +- 0.05 nm [5] ; [10].
4845,10.1002/app.41984,something_else,"Competitive adsorption of Cu2+, Pb2+, and Cd2+ wit ... tion in the solutions was measured using the FAAS."
4846,10.1002/app.41984,something_else,"The adsorption abilities of Cu2+ onto PAESK-C-Na,  ... ation in the filtrate was measured using the FAAS."
4847,10.1002/app.41984,something_else,Relative molecular weight was obtained using Gel p ... 5-μm filter membrane before injected into the GPC.
4848,10.1002/app.41984,something_else,The thermal degradation processes were investigate ... ing rate of 10degC/min ranging from 20 to 700degC.
4849,10.1002/app.41984,something_else,"Polymer samples (1 g) were dissolved into NMP (10  ... olor, with the thickness ranging from 30 to 50 μm."
4850,10.1002/app.41984,something_else,Polymerization was conducted in the liquid phase w ... es of polymers were briefly presented in Scheme 1.
4851,10.1002/app.41984,something_else,"DPA, BPA, DCDPS, anhydrous potassium carbonate (K2 ... prepared by successive dilution of stock solution."
4852,10.1016/j.apsusc.2005.12.016,something_else,A 5 μL droplet of the colloidal solution has been  ... d of 0.2 T corresponds to the onset of saturation.
4853,10.1016/j.chemosphere.2014.04.065,something_else,NF-κB DNA binding activity was examined with elect ... ng activity was quantified by gray scale scanning.
4854,10.1016/j.cej.2009.04.021,something_else,The reagent used as coagulant was commercial ferri ... ation conditions are fully described in Ref. [20].
4855,10.1016/j.cattod.2009.10.018,something_else,"The experiments were performed with puriss 3,3 dim ...  transfers were made under Schlenk techniques[38]."
4856,10.1016/j.conbuildmat.2016.06.121,something_else,The thin-layer chromatography with flame ionizatio ... altenes) was performed with a three-stage process.
4857,10.1016/j.conbuildmat.2016.06.121,something_else,Fourier transform infrared spectrometry (FTIR) was ... ed onto the KBr table and dried for FTIR analysis.
4858,10.1016/j.conbuildmat.2016.06.121,something_else,"Viscosity of aged asphalt was measured by DSR, and ... 100 degC and 120 degC) were measured in this test."
4859,10.1016/j.conbuildmat.2016.06.121,something_else,The asphalt binder obtained from field was extract ...  asphalt binder from asphalt mixture was obtained.
4860,10.1016/j.conbuildmat.2016.06.121,something_else,Conventional TFOT test was used to simulate the sh ... halt binder in service life between 1 and 8 years.
4861,10.1016/j.biortech.2015.01.078,something_else,"As a comparison, the DO removal from seawater was  ... rogen was allowed to escape via a small vent hole."
4862,10.1016/j.biortech.2015.01.078,something_else,Deoxygenation was carried out in a cell made of tr ... ) seawater flowed through the cathode compartment.
4863,10.1016/j.chemosphere.2014.04.065,something_else,"Levels of TNF-α, IL-6, IL-4 and IFN-γ in BALF and  ... ord Protein Assay Kit (Beyotime, Shanghai, China)."
4864,10.1016/j.biortech.2015.01.078,something_else,The anodic chamber (as described in Section 2.1) o ... ned at +250 mV (vs Ag/AgCl) throughout this study.
4865,10.1007/s10008-015-2785-z,something_else,All reagents used in this experiment were of analy ... s that the weight ratio of K3Fe(CN)6 to GO is 1:2.
4866,10.1016/j.cej.2009.04.021,something_else,LC-separations were carried out with a Hypersil Go ... S mode as described by Gebhardt and Schroder [20].
4867,10.1016/j.cej.2009.04.021,something_else,For elimination and/or degradation monitoring by A ... eping constant temperature of 240 degC for 15 min.
4868,10.1016/j.cej.2009.04.021,something_else,Commercially available solid phase extraction (SPE ... hen evaporated and following concentrated to 1 ml.
4869,10.1016/j.cej.2009.04.021,something_else,"Turbidity, BOD5, COD, total, fixed and volatile so ...  test was performed according to Kang et al. [23]."
4870,10.1016/j.cej.2009.04.021,something_else,In a second step was evaluated the efficiency of p ... r treatment the sample was collected and analyzed.
4871,10.1016/j.cej.2009.04.021,something_else,A photoreactor was arranged for the experiments in ... ) was continuously mixed using a magnetic stirrer.
4872,10.1016/j.cej.2009.04.021,something_else,The tests were carried out under optimum reagent s ... y the DAF process was subsequently treated by AOP.
4873,10.1007/s10008-015-2785-z,something_else,To evaluate the electrochemical properties of the  ... aterial in the working electrode was about 2.0 mg.
4874,10.1016/j.jcis.2015.06.014,something_else,"After aging, the reaction product was collected by ... under ambient air and does not hydrolyze in water."
4875,10.1016/j.jcis.2015.06.014,something_else,"Additional experiments to study the influence of t ... NH2OH[?]HCl reducing agent solution, respectively."
4876,10.1016/j.jcis.2015.06.014,something_else,The 100-fold up-scaling was realized in an automat ... rom green to orange as a result of Cu2O formation.
4877,10.1002/rcm.7197,something_else,Polymer samples were dissolved in THF at a concent ... he target was inserted into the mass spectrometer.
4878,10.1002/rcm.7197,something_else,"Polystyrenes were purchased from Polymer Standard  ... purchased from Sigma-Aldrich (Steinheim, Germany)."
4879,10.1016/j.tsf.2015.01.031,something_else,Molybdenum carbonitride coatings were deposited in ... bic centimetres per minute) to the vacuum chamber.
4880,10.1016/j.chroma.2014.08.054,something_else,For the clean-up step we chose a multi-well plate  ... ysates were used for the validation of the method.
4881,10.1016/j.chroma.2014.08.054,something_else,The concentrations of individual stock solutions o ... andard were prepared following the same procedure.
4882,10.1016/j.chroma.2014.08.054,something_else,"Murine embryonic fibroblasts were incubated (37 de ... sie brilliant blue G-250, Bio-Rad, Hercules, USA)."
4883,10.1016/j.chroma.2014.08.054,something_else,The optimized chromatographic separation selected  ... eviously discarded due to their negligible effect.
4884,10.1016/j.chroma.2014.08.054,something_else,Individual stock solutions of the compounds under  ... biological samples and clean-up process were used.
4885,10.1016/j.chroma.2014.08.054,something_else,"Mobile phases were filtered under low-pressure and ... n membranes (47 mm, 0.2 μm pore size, Phenomenex)."
4886,10.1016/j.chroma.2014.08.054,something_else,"Commercially available camptothecin was purchased  ... i-Q Direct 8 system (Millipore, Molsheim, France)."
4887,10.1016/j.chroma.2014.08.054,something_else,"The liquid chromatographic system (Merck-Hitachi,  ... s were injected through a Rheodyne 7725i injector."
4888,10.1016/j.jcat.2013.08.016,something_else,Textural and structural properties of monoliths we ... with an EDS instrument for compositional analysis.
4889,10.1016/j.jcat.2013.08.016,something_else,Cr-doped monoliths (cut in order to obtain slices  ...  the samples were cooled down to room temperature.
4890,10.1016/j.jcat.2013.08.016,something_else,Reference Cr/aerosil samples were prepared by impr ... asurements and the latter for UV-Vis spectroscopy.
4891,10.1016/j.jcat.2013.08.016,something_else,Tetraethyl orthosilicate (TEOS) was added to a mix ... degC) was obtained by a Millipore Direct Q system.
4892,10.1016/j.enconman.2012.07.010,something_else,"Fuel B30 (70% fossil diesel fuel, 30% pure biofuel ...  periodically while running on fossil diesel fuel."
4893,10.1016/j.enconman.2012.07.010,something_else,"For storage tests, mixtures containing 68% C. sati ...  were performed using the following fuel mixtures:"
4894,10.1002/0471238961.0209191303080107.a01,something_else,The washed slime is dried and melted to produce sl ... tter is transferred to the bismuth refining plant.
4895,10.1002/0471238961.0209191303080107.a01,something_else,Bismuth is leached from roasted tin concentrates a ... e oxychloride method requires additional refining.
4896,10.1002/0471238961.0209191303080107.a01,something_else,The alloy of bismuth and lead from the separation  ... s is also used to remove these elements from lead.
4897,10.1002/0471238961.0209191303080107.a01,something_else,Bismuth pellets range from 4.5 to 60 g in size and ... tity of bismuth must be added regularly to a melt.
4898,10.1002/anie.200501650,something_else,The Pd-Sb-Bi/TiO2 catalysts were prepared by impre ... 9900 (energy dispersive X-ray spectroscopy (EDX)).
4899,10.1016/j.chroma.2014.07.057,something_else,Chromatograms of enantioseparation of racemic arom ... : 10 degC; stationary phase retention: 43.5-47.5%.
4900,10.1016/j.chroma.2014.07.057,something_else,Chromatograms of enantioseparation of racemic arom ... ture: 10 degC; stationary phase retention: 15-20%.
4901,10.1016/j.chroma.2014.07.057,something_else,Note: 50 mmol L-1 of N-n-dodecyl-l-proline was add ... sition metal ion with pH5.6; temperature: 10 degC.
4902,10.1016/j.chroma.2014.07.057,something_else,The chiral analysis of racemates and HSCCC fractio ... degC during separation unless otherwise specified.
4903,10.1016/j.chroma.2014.07.057,something_else,Recovery of enantiomer from separated fractions of ... educed pressure to give the recovered enantiomers.
4904,10.1016/j.chroma.2014.07.057,something_else,Both of analytical and preparative separations wer ... tion was conducted in a head-to-tail elution mode.
4905,10.1016/j.chroma.2014.07.057,something_else,(1) 200 mL of organic solvent and 200 mL of water  ...  the two phases were separated shortly before use.
4906,10.1016/j.enconman.2012.07.010,something_else,Pork lard methyl esters were produced from pork la ...  esters did not contain any antioxidant additives.
4907,10.1016/j.chroma.2014.07.057,something_else,The equilibrium experiments were performed in 10 m ... l concentration of enantiomers in the lower phase.
4908,10.1016/j.chroma.2014.07.057,something_else,The chiral ligand N-n-dodecyl-l-proline was synthe ... remove a small amount of n-decanal in the residue.
4909,10.1016/j.chroma.2014.07.057,something_else,"Mandelic acid, 4-bromomandelic acid, 4-methoxymand ...  grade. Water used for HPLC study was redistilled."
4910,10.1016/j.chroma.2014.07.057,something_else,"Two different models of HSCCC apparatus were used: ... u, China) was employed to record the chromatogram."
4911,10.1016/0040-4039(80)88098-1,something_else,"At 1096degC in a base-washed, quartz flow system ( ... c pathways are discussed (eqs 1 and 2 inter alia)."
4912,10.1016/j.jpowsour.2005.03.045,something_else,"Powder X-ray diffraction (XRD, Rint-2000, Rigaku,  ... g that there were no leaks during the experiments."
4913,10.1016/j.electacta.2013.05.073,something_else,Four batches of SnO2 were produced: (i) 280 degC f ... ation were given in previous report [26] and [27].
4914,10.1016/j.electacta.2013.05.073,something_else,"In order to prepare tin oxide (SnO2), the molten s ... imilar to our previous studies on CuO by MSM [25]."
4915,10.1016/j.chroma.2014.07.057,something_else,The biphasic solvent system was prepared as the fo ... the organic phase for the biphasic solvent system.
4916,10.1016/j.enconman.2012.07.010,something_else,C. sativa oil was obtained from C. sativa seed by  ...  water from the esters was evaporated in a vacuum.
4917,10.1016/j.enconman.2012.07.010,something_else,Rapeseed oil methyl esters (RMEs) were purchased f ...  of Agriculture were also used in the experiments.
4918,10.1016/j.physe.2011.01.001,something_else,The degradation of methyl orange was carried out b ... h commercial ZnS powder under the same conditions.
4919,10.1016/j.matchemphys.2016.05.031,something_else,Disk-shaped specimens of Mg-7.8Al-0.68Zn-0.18Mn (A ... nterface after the above corrosion immersion test.
4920,10.1016/j.powtec.2015.01.050,something_else,The DC electrical conductivity of the nanofluids w ... ch larger than that of the base fluid (σp [?] σ0).
4921,10.1016/j.poly.2006.09.023,something_else,"Acetonitrile (Aldrich, spectroscopy grade) used fo ... ) and the auxiliary electrode was a platinum wire."
4922,10.1016/j.poly.2006.09.023,something_else,"Triethylamine (2 mL) was added to a solution of is ... , 3.90 (s, 4H), 3.30 (m, 2H). MS: m/z 558 [M+Na]+."
4923,10.1016/j.poly.2006.09.023,something_else,"Paraformaldehyde (1.79 g, 0.06 mol) was added to a ... , 3.52 (s, 2H), 2.87 (s, 2H). MS: m/z 429 [M-H+]-."
4924,10.1016/j.poly.2006.09.023,something_else,All reactions and operations related to organometa ... epared according to the literature procedure [27].
4925,10.1007/s10853-009-3909-6,something_else,"After cooling, the specimens were cut perpendicula ... aOH solution so as to reveal the interfacial area."
4926,10.1016/j.supflu.2014.08.014,something_else,Supercritical deposition (SCD) is used to prepare  ...  electrocatalysts prepared using different routes.
4927,10.1007/s10853-009-3909-6,something_else,The aluminium-silicon alloys used are prepared in  ... g in an alumina crucible prior to drop deposition.
4928,10.1016/j.jeurceramsoc.2017.01.004,something_else,Cracks were healed ex-situ at 600 degC for 16 h in ... re was based on observations by Gupta et al. [10].
4929,10.1016/j.biortech.2014.03.082,something_else,A series of ammonia percolation experiments were p ... content before and after the ammonia pretreatment.
4930,10.1016/j.biortech.2014.03.082,something_else,Monosaccharides were derivatised for GC as describ ...  standards with myo-inositol as internal standard.
4931,10.1016/j.biortech.2014.03.082,something_else,The extracted lignin containing polysaccharide imp ...  with acidified water (HCl pH 2) and freeze dried.
4932,10.1016/j.biortech.2014.03.082,something_else,The liquor was reduced in pH to 7-8 by evaporation ... hed three times with HCl at pH 2 and freeze dried.
4933,10.1016/j.biortech.2014.03.082,something_else,"The percolation device, inspired by previous works ... ed lignin was recovered by precipitation in water."
4934,10.1016/j.biortech.2014.03.082,something_else,A stainless steel reactor (75 ml) was packed with  ... ed lignin was recovered by precipitation in water.
4935,10.1016/j.biortech.2014.03.082,something_else,The poplar sawdust was subjected to batch and perc ... r. The multistep process is illustrated in Fig. 1.
4936,10.1016/j.jeurceramsoc.2017.01.004,something_else,"Isothermal oxidation kinetics were investigated by ... conducted in Ar (purity > 5N, 50 sccm) atmosphere."
4937,10.1016/j.chroma.2012.02.034,something_else,A simple and cost-effective method of dynamic micr ... r compared with the traditional extraction method.
4938,10.1016/j.supflu.2014.08.014,something_else,Vulcan XC-72R (Vulcan) was obtained from Cabot Int ... obtained from Riedel de Haen and used as received.
4939,10.1016/j.supflu.2014.08.014,something_else,After the system reached adsorption equilibrium in ... ngs were measured gravimetrically after each step.
4940,10.1016/j.physe.2011.01.001,something_else,"X-ray diffraction (XRD, BDX3200, China) and energy ...  scanning electron microscopy (SEM, TESCAN VEGA2)."
4941,10.1016/j.fuel.2012.03.026,something_else,"One hundred and twenty-two sets of compositional a ... ere 11%, 61%, 30%, 38%, 14%, and 29% respectively."
4942,10.1016/j.electacta.2008.02.080,something_else,The silver disk electrode was mechanically polishe ...  surface. The modified electrode was dried in air.
4943,10.1016/j.electacta.2008.02.080,something_else,The CSNs were prepared according to the literature ... orage for months after the purification procedure.
4944,10.1016/j.electacta.2008.02.080,something_else,All glassware used in the following procedures was ...  use. Stock Solutions were stored in dark bottles.
4945,10.1016/j.electacta.2008.02.080,something_else,"Electrochemical measurements were performed on a C ... th a UV-vis 3010 Spectrophotometer (Tokyo, Japan)."
4946,10.1016/j.electacta.2008.02.080,something_else,Horse heart Cyt. c and bovine serum album (BSA) we ... tion apparatus. Its resistivity was over 18 MΩ cm.
4947,10.1016/j.supflu.2014.08.014,something_else,Supercritical deposition experiments were carried  ...  converted to elemental Pt via 3 different routes.
4948,10.1016/j.matlet.2014.12.034,something_else,The RHs used in this research were obtained from G ... hou Chemical Reagent Company and used as received.
4949,10.1016/j.cattod.2006.05.017,something_else,"Catalysts were prepared by the ""organic procedure"" ... o in precursors was confirmed by means of SEM-EDX."
4950,10.1016/j.supflu.2014.08.014,something_else,Pt-based electrocatalysts for polymer electrolyte  ... lls prepared by supercritical deposition technique
4951,10.1016/j.supflu.2014.08.014,something_else,"Among the catalysts, highest ESA (92.2 m2/g) was o ... 1 < SCC-2 and SCC-1 < SCC-3 < SCC-2, respectively."
4952,10.1016/j.supflu.2014.08.014,something_else,The performances of the MEAs were determined in a  ...  mV s-1 from the open cell voltage value to 0.1 V.
4953,10.1016/j.supflu.2014.08.014,something_else,Nafion(r)117 was used as the polymer electrolyte m ... s 0.5 mg Pt cm-2 for both anode and cathode sides.
4954,10.1016/j.supflu.2014.08.014,something_else,The electrochemical characterization of these cata ... f the carbon support that usually occurs at 1.2 V.
4955,10.1016/j.supflu.2014.08.014,something_else,The prepared catalysts were characterized by IR sp ... t resolution of <0.19 nm in phase contrast images.
4956,10.1016/j.supflu.2014.08.014,something_else,"In the second route, after the system reached adso ... sured gravimetrically using an analytical balance."
4957,10.1016/j.matlet.2014.12.034,something_else,Photoluminescent mesoporous carbon-doped silica wa ... alcination of HCl treated RHs at 550 degC for 6 h.
4958,10.1016/j.chroma.2012.02.034,something_else,Sample preparation is one of the most important st ... ent consumption and manual handling were enhanced.
4959,10.1016/j.chroma.2012.02.034,something_else,"The standards (purity > 98.5%) of ametryn, atrazin ... C for 1 h to eliminate organic matter before used."
4960,10.1016/j.chroma.2012.02.034,something_else,Individual triazine stock solutions (200 μg mL-1)  ... n order to prevent the decomposition of triazines.
4961,10.1016/j.eurpolymj.2014.07.033,something_else,"The amounts of components (Table 1): The concentra ... onomer, NIPAm and are not part of the sample name."
4962,10.1016/j.eurpolymj.2014.07.033,something_else,Nanocomposite super-porous poly(N-isopropylacrylam ...  to times of gelation of the respective mixtures).
4963,10.1016/j.eurpolymj.2014.07.033,something_else,"N-isopropylacryl amide (NIPAm), N,N'-Methylenebisa ... purchased from Sigma-Aldrich and used as received."
4964,10.1016/j.msea.2017.05.046,something_else,"Commercially pure metals (Ti 99.8 wt%, Sn 99.99 wt ... m focused ion beam (FIB, Hitachi FB2000A) milling."
4965,10.1002/jcp.21265,something_else,Sedimentation profile of TNF and HDLs. ECVTNF cell ... pernatant before centrifugation) of TNF and apoA1.
4966,10.1002/jcp.21265,something_else,Cholesterol efflux accounts for HDL effect. TNF ac ... ontrol; **P = 0.0012 versus control without apoA1.
4967,10.1002/jcp.21265,something_else,"HDLs activate the shedding of TNF from isolated pl ...  described in the ""Materials and Methods"" section."
4968,10.1016/j.eurpolymj.2014.07.033,something_else,"The porous morphology of the hydrogels, as well as ... e microscope by gluing with a small drop of water."
4969,10.1002/jcp.21265,something_else,COS-7 and H9C2 cells were transiently transfected  ... e measured by ELISA. Values represent means +- SD.
4970,10.1002/jcp.21265,something_else,"Plasma membranes of ECVTNF cells were prepared as  ... e supernatant were pelleted at 48,000g for 30 min."
4971,10.1002/jcp.21265,something_else,Lipid rafts were isolated by sucrose density gradi ... d fractions were analyzed by immunoblot and ELISA.
4972,10.1002/jcp.21265,something_else,"The monkey kidney fibroblast cell line COS-7, the  ... ium and experiments were performed in this medium."
4973,10.1002/jcp.21265,something_else,"Human HDLs (density range 1.063-1.21 g/ml) were is ... he Limulus test (Nelson Labs, Salt Lake City, UT)."
4974,10.1016/j.apcata.2007.06.013,something_else,Thermo-gravimetric analysis (TGA) in oxidative atm ... mL min-1 of air and 10 degC min-1 of heating rate.
4975,10.1016/j.apcata.2007.06.013,something_else,"BET specific surfaces were measured in a Sorptomat ... , before being exposed to the analysis conditions."
4976,10.1016/j.apcata.2007.06.013,something_else,Hydrodenitrogenation of pyridine was tested in con ... then passivated before exposure to the atmosphere.
4977,10.1016/j.apcata.2007.06.013,something_else,The carburised catalysts were prepared using the t ... al composition rather than the phase compositions.
4978,10.1002/jcp.21265,something_else,"For cholesterol extraction, a mixture of isopropan ... eviously described (Beaumier-Gallon et al., 1998)."
4979,10.1016/j.actbio.2013.03.015,something_else,"To analyze collagen organization and orientation,  ... d light microscopy (BX-60, Olympus, Tokyo, Japan)."
4980,10.1016/j.eurpolymj.2014.07.033,something_else,For the characterization of nanofiller distributio ... degC under vacuum for 24 h and broken at -80 degC.
4981,10.1016/j.eurpolymj.2014.07.033,something_else,The value of mass(theoretical) was calculated from ... ter until mass constancy at 100 degC under vacuum.
4982,10.1002/jcp.25000,something_else,"For epigenetic analysis, confluent HC11 cells were ... ep; LKT Laboratories, Inc. St. Paul, MN) for 48 h."
4983,10.1002/jcp.25000,something_else,"HC11 and EpH4, normal mouse mammary epithelial cel ... (1 μM), insulin (5 μg/ml) and prolactin (9 μg/ml)."
4984,10.1002/jcp.25000,something_else,"ICR mice were purchased from SLC (Shizuoka, Japan) ... glands were frozen immediately and stored -80degC."
4985,10.1016/j.cej.2009.04.022,something_else,"A reactive distillation unit, suitable for the syn ... able for the process scale up and intensification."
4986,10.1016/j.cej.2009.04.022,something_else,The organic phase composition indicates excellent  ... or by adding a defined amount of acetic anhydride.
4987,10.1016/j.cej.2009.04.022,something_else,"However, the ion-exchanger is thermally stable up  ... as used for the reactive distillation experiments."
4988,10.1016/j.cej.2009.04.022,something_else,The reaction mixture was fed at atmospheric pressu ... endence on time coordinate W/F is shown in Fig. 2.
4989,10.1016/j.cej.2009.04.022,something_else,"Another set of experiments was performed in a lab  ...  water phase, being withdrawn as overhead streams."
4990,10.1016/j.eurpolymj.2014.07.033,something_else,The mass of the swollen gel was measured after the ... niform size of 10 mm in diameter and 10 mm height.
4991,10.1016/j.cej.2009.04.022,something_else,"A fixed-bed reactor (i.d. 30 mm, length 0.5 m) wit ... bed of catalyst was maintained in all experiments."
4992,10.1016/j.cej.2009.04.022,something_else,The most common strategy of producing ethyl acetat ... elective separation of ethyl acetate is desirable.
4993,10.1016/j.cej.2009.04.022,something_else,The esterification of acetic acid (AA) and ethanol ... kept slightly increasing in a rate of 4% per year.
4994,10.1016/j.conbuildmat.2016.03.149,something_else,"In the study on bottom ash metakaolin based geopol ...  of 1, 3, 7 and 28 days for all the mixes studied."
4995,10.1016/j.conbuildmat.2016.03.149,something_else,A combination of sodium silicate solution and sodi ... dissolved in distilled water to make the solution.
4996,10.1016/j.conbuildmat.2016.03.149,something_else,Results showed that Liquid to Solid ratio 0.5 exhibits effective compressive strength in mortar.
4997,10.1016/j.ssc.2009.05.020,something_else,Two cubic Ga1-xMnxN films about 0.3 μm thick with  ... he structure of a zinc-blende type for both films.
4998,10.1016/j.eurpolymj.2014.07.033,something_else,The ash analyses were performed as follows: The dr ... e with the ash. The dry TiO2 ash was then weighed.
4999,10.1016/j.eurpolymj.2014.07.033,something_else,"The partial gel fraction of the nanofiller, w(f),  ... e by the theoretical TiO2 content in the specimen."
5000,10.1016/j.cej.2009.04.022,something_else,"The separation of reaction water from the reaction ...  acetic anhydride is used, instead of acetic acid."
5001,10.1016/j.matlet.2007.12.039,something_else,The solubility study of NBS was done in methanol a ... tals of NBS were obtained after one week (Fig. 1).
5002,10.1016/j.actbio.2013.03.015,something_else,"For visualization of the ECM structure, immunocyto ... and processed using Adobe Photoshop 10.0 software."
5003,10.1016/j.actbio.2013.03.015,something_else,"Unstrained cells were maintained identically to th ... P Bioscience, Solon, OH) were added to the medium."
5004,10.1007/s11665-017-2502-4,something_else,Selected test specimens were then sectioned and mo ... crostructural refinement as the builds progressed.
5005,10.1007/s11665-017-2502-4,something_else,An Instron(r) CEAST 9050 impact tester was used to ... e indents were taken in each location of interest.
5006,10.1016/j.matlet.2006.06.062,something_else,Freeze-dried microspheres (90 mg) were dispersed i ... calculated in terms of cumulative release (% w/w).
5007,10.1016/j.matlet.2006.06.062,something_else,Gentamicin loading in composite microspheres and e ... that of initial drugs before encapsulated by PHBV.
5008,10.1016/j.matlet.2006.06.062,something_else,10 ml of gentamicin solution with two concentratio ... ure was freeze-dried overnight and kept at 4 degC.
5009,10.1016/j.matlet.2006.06.062,something_else,The hydroxyapatite nanoparticles were prepared by  ... dried overnight and calcined at 500 degC for 28 h.
5010,10.1016/j.matlet.2006.06.062,something_else,Polyhydroxybutyrate-co-hydroxyvalerate (PHBV) with ... All other chemicals used were of analytical grade.
5011,10.1111/j.1440-1819.2007.01654.x,something_else,"where, dose = dosage of lithium in mmol (300 mg li ... F = fraction absorbed (1.0) and k = 0.693/t1/2_Li."
5012,10.1016/j.jpowsour.2006.11.090,something_else,"For Pt-exchanged zeolites, 3 g of zeolite HY was w ... olite-Nafion composite membrane is denoted as PZN."
5013,10.1016/j.chroma.2012.02.034,something_else,"In brief, the best experimental conditions for all ... ent solvent and 0.15 g mL-1 of salt concentration."
5014,10.1016/j.chroma.2012.02.034,something_else,"In this study, the 1-dodecanol was employed in the ... olume of the collected 1-dodecanol could increase."
5015,10.1016/j.chroma.2012.02.034,something_else,"Lastly, the volume of the extraction solvent was i ...  mL methanol-water solutions (10%, v/v) were used."
5016,10.1016/j.chroma.2012.02.034,something_else,The classical sample preparation technique for ext ... s were injected into the HPLC system for analysis.
5017,10.1016/j.chroma.2012.02.034,something_else,"Finally, 1.5 g sodium chloride was added to the co ... diluted to 200 μL with methanol for HPLC analysis."
5018,10.1016/j.chroma.2012.02.034,something_else,"Subsequently, the vacuum pump was activated and 1  ... stopped, and the extraction process was completed."
5019,10.1016/j.chroma.2012.02.034,something_else,"Firstly, the cereal sample was accurately weighed  ... the ports of the vacuum SPE manifold by T1 and T2."
5020,10.1016/j.chroma.2012.02.034,something_else,"The DMAE-SFO system is represented in Fig. 2, whic ... 00.0 mm long, 0.5 mm i.d.), respectively (Fig. 2)."
5021,10.1016/j.chroma.2012.02.034,something_else,"For recovery studies, spiked cereal samples were p ... an 24 h until methanol has volatilized completely."
5022,10.1016/j.chroma.2012.02.034,something_else,Different volumes of 1-dodecanol in the range of 5 ... μL 1-dodecanol was used in the subsequent studies.
5023,10.1016/j.actbio.2013.03.015,something_else,Cell images were obtained using phase-contrast mic ... ed using Cell Profiler software (Broad Institute).
5024,10.1016/j.jpowsour.2006.11.090,something_else,"A commercial E-TEK electrode (30 wt.% Pt/C, 0.5 mg ... f 3 t to form a membrane-electrode assembly (MEA)."
5025,10.1016/j.jpowsour.2006.11.090,something_else,The water generation capability of the PZN composi ... idifying capability of the PZN composite membrane.
5026,10.1016/j.actbio.2013.03.015,something_else,"In subconfluent conditions, cells were removed fro ... ic stretch of 24 h was applied as shown in Fig. 2."
5027,10.1016/j.actbio.2013.03.015,something_else,Primary osteoblasts were isolated from newborn mou ... a University Committee for Animal Experimentation.
5028,10.1016/j.jhazmat.2009.07.048,something_else,"A direct chlorination of synthetic samples, prepar ... ion of around 1600 μgCCl3 l-1 (measured as THMFP)."
5029,10.1016/j.jhazmat.2009.07.048,something_else,Coagulation-flocculation-decantation experiments w ... on of flocs and their later decantation after 2 h.
5030,10.1016/j.jhazmat.2009.07.048,something_else,Adsorption onto powdered activated carbon (PAC) tr ...  area of 1000 m2 g-1 and a particle size of 40 μm.
5031,10.1016/j.jhazmat.2009.07.048,something_else,"The generator produced 12 mgO3 min-1, which was mo ... d ozone was 3 mgO3 l-1, according to the equation:"
5032,10.1016/j.jhazmat.2009.07.048,something_else,The pH was checked by a pHmeter (Crison 507) and t ...  the 4500-Cl and 4500-B Methods [15] respectively.
5033,10.1016/j.jhazmat.2009.07.048,something_else,"In this study, synthetic samples were prepared due ... prepared in order to evaluate the THMFP parameter."
5034,10.1016/j.jpowsour.2006.11.090,something_else,The particle size of the Pt/zeolite was determined ...  used to determine the ratio of Pt in the zeolite.
5035,10.1016/j.biortech.2010.07.019,something_else,"The reusability of Ca-alginate immobilized G. oxyd ...  substrates, and products in successive operation."
5036,10.1016/j.biortech.2010.07.019,something_else,The samples were taken periodically from reactor a ... were identified by comparison with known standard.
5037,10.1016/j.biortech.2010.07.019,something_else,"To determine dry cell weight (DCW), 100 ml culture ... n: DCW (g/l) = 0.579OD600 nm + 0.008 (R2 = 0.997)."
5038,10.1016/j.biortech.2010.07.019,something_else,The immobilized cells (25 beads) were added to the ... vity was designed as yields (g/l) of benzaldehyde.
5039,10.1016/j.biortech.2010.07.019,something_else,G. oxydans cells were harvested by centrifugation  ... and the high OD600 nm indicated the low stability.
5040,10.1016/j.biortech.2010.07.019,something_else,"G. oxydans M5/ALDH ( Wei, 2008) was used for the b ...  degC) until late exponential growth phase (20 h)."
5041,10.1016/j.biortech.2010.07.019,something_else,Benzyl alcohol and benzaldehyde were obtained from ...  analytical grade and were commercially available.
5042,10.1016/j.jpowsour.2006.11.090,something_else,"In this work, a novel Pt/zeolite-embedded Nafion p ... ned at 0.6 V with humidified reactants at 75 degC."
5043,10.1016/j.jpowsour.2006.11.090,something_else,Polarization curves of single cell using PZN membr ...  measured at 50 degC and 1 atm with dry H2 and O2.
5044,10.1016/j.biortech.2010.07.019,something_else,To consider both activity and stability comprehens ... ldehyde yield was 3.65 g/l and OD600 nm was 0.099.
5045,10.1016/j.matlet.2007.12.039,something_else,160 g of succinimide was dissolved in a mixture of ... ed by Fourier transform infra red (FTIR) analysis.
5046,10.1016/j.cej.2007.11.017,something_else,The segmented poly(ester urethane)s are insoluble  ... ane linkages and high molecular weight of polymer.
5047,10.1016/j.cej.2007.11.017,something_else,"Initially, bis-isocyanato-polyester was prepared f ...  60 degC was maintained throughout the experiment."
5048,10.1016/j.apcata.2007.06.012,something_else,Linoleic acid oligomerisation was studied in a pre ... tored under nitrogen atmosphere prior to analysis.
5049,10.1016/j.apcata.2007.06.012,something_else,The specific surface areas of the catalysts were m ...  The catalysts were outgassed at 200 degC for 4 h.
5050,10.1016/j.apcata.2007.06.012,something_else,Na-MCM-41 was synthesized by using the method desc ... ed after calcination of this material at 530 degC.
5051,10.1016/j.apcata.2007.06.012,something_else,The used zeolites were supplied by Zeolyst Interna ... tes were ion-exchanged to NH4-form with 3 M NH4Cl.
5052,10.1016/j.molbrainres.2004.10.041,something_else,"Real-time RT-PCR was performed with the ABI Prism  ... CGGCA; Nav1.5 probe, CCATCGTGAACAACAAGAGTGAGTGCGA."
5053,10.1016/j.molbrainres.2004.10.041,something_else,Reverse transcription was identical to the method  ...  until used for either gel-based or real-time PCR.
5054,10.1016/j.molbrainres.2004.10.041,something_else,"Following electrophysiological recording, isolated ...  then stored overnight (-80 degC) prior to RT-PCR."
5055,10.1016/j.molbrainres.2004.10.041,something_else,"Individual medial septum/nucleus of the diagonal b ... btained from Sigma, St. Louis MO, except as noted."
5056,10.1016/j.apcata.2007.06.012,something_else,The samples were analyzed by SEC-HPLC technique. T ...  acids and kept at 4 degC prior to their analysis.
5057,10.1016/j.fuproc.2014.06.004,something_else,The standard compounds of phenols were directly in ... ated using an external standard line in the GC/MS.
5058,10.1016/j.fuproc.2014.06.004,something_else,With two pieces of quartz wool placed at the top a ... gible for temperatures higher than 1000 degC [22].
5059,10.1016/j.fuproc.2014.06.004,something_else,Each of the raw coal samples (2.00 g) was extracte ... . The extract yield (wt%) is expressed as follows:
5060,10.1016/j.fuproc.2014.06.004,something_else,"Seven species of common phenolic compounds were an ...  Fine Chemical Research Institute, Tianjin, China."
5061,10.1016/j.fuproc.2014.06.004,something_else,"ad: air dried basis; daf: dry and ash-free basis; St, ad: total sulfur (air dried basis)."
5062,10.1016/j.fuproc.2014.06.004,something_else,"Four coal samples including lignite (coal A), long ... , and the analytical values are listed in Table 1."
5063,10.1016/j.actbio.2013.03.014,something_else,Radiopacity of disc-shaped strontium(II)-containin ... ity referring to a 0.5 mm step aluminium standard.
5064,10.1016/j.actbio.2013.03.014,something_else,"Samples for ToF-SIMS analysis were removed from th ... e detector, the 44Ca was used for data evaluation."
5065,10.1016/j.actbio.2013.03.014,something_else,"For Sr2+-release experiments and ToF-SIMS analyses ...  from a Sr2+ standard (Merck, Darmstadt, Germany)."
5066,10.1016/j.fuproc.2014.06.004,something_else,"The pyrolyzed non-condensable volatiles, without t ... y for phenols when entering the mass spectrometer."
5067,10.1016/j.actbio.2013.03.014,something_else,"For mechanical characterization, the cement pastes ... h a 10 kN load cell (Instron, Darmstadt, Germany)."
5068,10.1016/j.apcata.2007.06.012,something_else,"The sample was diluted with acetone and dried unde ...  Additionally, the samples were analyzed by GC-MS."
5069,10.1007/s10800-013-0589-3,something_else,"Tetraethylorthosilicate (TEOS), N-[3-(trimethoxysi ... truments Electrochemical Workstation (Model-760D)."
5070,10.1016/j.actbio.2010.09.019,something_else,A similar prescription is also used to assess the  ... d easily add new layers after predetermined times.
5071,10.1016/j.fuproc.2015.01.010,something_else,The fusel oil used in this study was supplied from ... e number of the fusel oil is higher than gasoline.
5072,10.1016/j.renene.2011.06.022,something_else,"Effect of variation of initial pH on cell has been ... , 4.4 mL (13.24) and 4.8 mL (13.28), respectively."
5073,10.1016/j.renene.2011.06.022,something_else,"Effect of variation of reductant on cell has been  ... x 10-4 M) and 1.6 mL (6.4 x 10-4 M), respectively."
5074,10.1016/j.renene.2011.06.022,something_else,"Effect of variation of dye photo sensitizer on cel ... x 10-5 M) and 2.1 mL (8.4 x 10-5 M), respectively."
5075,10.1016/j.renene.2011.06.022,something_else,"A photogalvanic cell consisting of 1.8 mL of M/100 ... L) = 45 mm, and Pt electrode area = 0.4 x 0.2 cm2."
5076,10.1016/j.renene.2011.06.022,something_else,"Initial pH of reaction mixture has been calculated ... arimeter Model-501 Cell (Surya, Ahmedabad, India)."
5077,10.1016/j.renene.2011.06.022,something_else,Photogalvanic cell is made of glass tube of H-shap ... of electrodes are connected to a digital pH meter.
5078,10.1016/j.apcata.2007.06.012,something_else,A reversed-phase liquid chromatographic technique  ... ere analysed by 1H-NMR (JEOL JNM-LA400) and GC-MS.
5079,10.1016/j.renene.2011.06.022,something_else,"Solutions, Rhodamine B dye (M/1000, i.e., concentr ...  colored containers to protect them from sunlight."
5080,10.1002/aoc.2959,something_else,The PZMS precursor was placed in a porcelain boat  ... r was collected after the furnace was cooled down.
5081,10.1002/aoc.2959,something_else,Divinylbis(cyclopentadienyl) zirconium Cp2Zr(CH=CH ... d dried to obtain the precursor as a brown powder.
5082,10.1002/aoc.2959,something_else,FT-IR spectra (KBr pellet) were recorded on a Nico ... ture were characterized using SEM (Hitachi S4800).
5083,10.1002/aoc.2959,something_else,"Sodium, bis(cyclopentadienyl) zirconium dichloride ... d used without further purification unless stated."
5084,10.1002/aoc.2959,something_else,Different PZMS precursors were prepared by adjusti ... ences with respect to the ratios of the reactants.
5085,10.1016/j.atherosclerosis.2005.01.007,something_else,To assess endothelium-dependent coronary vasomotor ...  percentage change versus control infusion (ClNa).
5086,10.1007/s10800-013-0589-3,something_else,Electrochemical measurements were conducted in a s ... 760D) in 0.1 M phosphate buffer solution (pH 7.2).
5087,10.1007/s10800-013-0589-3,something_else,Amine functionalized TPDT SSG covered SiO2 spheres ... indicated the formation of Au NPs on SiO2 spheres.
5088,10.1016/j.renene.2011.06.022,something_else,"Chemicals, Rhodamine B (90% Assay-Purity, Ases Che ...  Ltd., Mumbai, India) as indicator have been used."
5089,10.1016/j.jpowsour.2005.03.042,something_else,The second precursor used on the preparation of th ... e reagents were used without further purification.
5090,10.1016/j.actbio.2013.03.014,something_else,"To form a mouldable paste, cement powders were mix ... vent uncontrolled release of ions from the cement."
5091,10.1016/j.ijhydene.2007.09.001,something_else,"EtOH, ethanol; HAc, acetate; HPr, propionate; HBu, butyrate; HVa, valerate concentrations, mg-COD/L."
5092,10.1016/j.tet.2007.11.088,something_else,To a pre-cooled (-50 degC) solution of CuI (882 mg ... alcd for C30H52OSi: 456.3787. Found: m/z 456.3768.
5093,10.1016/j.tet.2007.11.088,something_else,To a solution of the crude oil in CH2Cl2 (10 mL) w ... alcd for C30H50OSi: 454.3631. Found: m/z 454.3637.
5094,10.1016/j.tet.2007.11.088,something_else,"To a solution of DMSO (680 μL, 9.58 mmol) in dry C ... -2-methyl-3-trimethylsilylcyclohexanone as an oil."
5095,10.1016/j.tet.2007.11.088,something_else,To a solution of a mixture (10:1) of 3a and 3b (1. ... ul flash column chromatography (hexane/AcOEt=7:1).
5096,10.1016/j.tet.2007.11.088,something_else,To a solution of the crude cyclohexanone derivativ ... e obtained by careful flash column chromatography.
5097,10.1016/j.tet.2007.11.088,something_else,"A mixture of (-)-(5R,6R)-6-methyl-5-trimethylsilyl ... , J=4.5 Hz), 7.21-7.33 (m, 3H), 7.36-7.46 (m, 2H)."
5098,10.1016/j.tet.2007.11.088,something_else,All solvents were obtained commercial sources and  ... med under Ar atmosphere with oven-dried glassware.
5099,10.1016/j.tet.2007.11.088,something_else,Infrared (IR) spectra were measured on a JASCO-FT/ ...  performed on a column with WAKO C-300 silica gel.
5100,10.1016/j.tet.2007.11.088,something_else,"To a solution of (+)-6 (446 mg, 0.98 mmol) in dry  ... calcd for C27H42O3: 382.3236. Found: m/z 382.3263."
5101,10.1016/j.tetlet.2014.06.064,something_else,Typical procedure for the preparation of compound  ... graphy (EtOAc/hexane) to get the pure compound 9g.
5102,10.1016/j.jmbbm.2012.02.018,something_else,Mesensphere mechanical properties were tested in a ...  modulus values for the MSC aggregate populations.
5103,10.1016/j.jmbbm.2012.02.018,something_else,"For histological analyses, mesenspheres were washe ...  Advanced v.4.5 software (Diagnostic Instruments)."
5104,10.1016/j.jmbbm.2012.02.018,something_else,Cellular organization and spheroid structure were  ... g electron microscope (Hitachi High Technologies).
5105,10.1016/j.jmbbm.2012.02.018,something_else,The spatial location of fluorescently-labeled MPs  ... BS) using a Zeiss LSM 510 NLO confocal microscope.
5106,10.1016/j.jmbbm.2012.02.018,something_else,MSC monolayers were re-suspended to obtain a singl ... spheres to Petri dishes on rotary orbital shakers.
5107,10.1016/j.jmbbm.2012.02.018,something_else,Human bone marrow-derived mesenchymal stem cells ( ...  Hanks' Balanced Salt Solution (Invitrogen/GIBCO).
5108,10.1016/j.jmbbm.2012.02.018,something_else,"Gelatin microparticles (MPs) were fabricated as pr ... f at least 10,000 events in a sample size of 1 mL."
5109,10.1016/j.optmat.2016.05.058,something_else,The bis(phenylvinyl)anthracene-based Polymers P1-3 ... E and Z configurations nonstereospecifically [36].
5110,10.1016/j.tetlet.2014.06.064,something_else,Typical procedure for the preparation of compound  ... hed with cold alcohol to get the pure compound 4d.
5111,10.1016/j.tsf.2015.01.037,something_else,Thin films were prepared using RF co-sputtering de ... g on applied RF sputtering power to the Sb target.
5112,10.1016/j.tet.2007.11.088,something_else,"A solution of dry FeCl3 (20 mg, 0.12 mmol) in dry  ... silyl ether was used in the next step immediately."
5113,10.1016/j.tet.2007.11.088,something_else,"To a solution of the crude 8 (58 mg) in MeOH (10 m ...  13 Hz), 4.62 (s, 1H), 5.12 (m, 4H), 5.62 (s, 2H)."
5114,10.1016/j.ijhydene.2007.09.001,something_else,The analytical procedures of Standard Methods [14] ... se indicated in our previous studies [7] and [15].
5115,10.1016/j.ijhydene.2007.09.001,something_else,Hydrogen production experiments were conducted in  ... nt was decanted and reseeded for another test run.
5116,10.1016/j.ijhydene.2007.09.001,something_else,"The substrate was xylose at a 20 g/L chemical oxyg ... H 2 O 5, CoCl 2 * 5 H 2 O 0.125, NaHCO 3 6720 [7]."
5117,10.1016/j.ijhydene.2007.09.001,something_else,"The seed sludge (dominated by Clostridium species, ... n to inhibit methane-producing bacterial activity."
5118,10.1016/j.renene.2014.02.036,something_else,Triglycerides (TG) react with dimethyl carbonate t ... ester until equilibrium was reached after 300 min.
5119,10.1016/j.renene.2014.02.036,something_else,a. Behaviour of potassium methoxide in Dimethyl ca ... um methoxide after stirring for 30 min at 90 degC.
5120,10.1016/j.renene.2014.02.036,something_else,"Influence of molar ratio of soybean oil to DMC on  ... lyst, reflux temperature 90 degC, pressure 1 atm)."
5121,10.1016/j.renene.2014.02.036,something_else,Transesterification of triglyceride with DMC requi ... olar ratio of 1:9 was chosen as the optimum value.
5122,10.1016/j.tet.2007.11.088,something_else,"To a solution of Pb(OAc)4 (340 mg, 0.76 mmol) in C ... , 1H, J=2.7, 10 Hz), 5.91 (dt, 1H, J=1.6, 9.7 Hz)."
5123,10.1016/j.renene.2014.02.036,something_else,Triglycerides conversion was monitored by Gel Perm ... ime of the sample with their respective standards.
5124,10.1016/j.renene.2014.02.036,something_else,"In the optimization work, the effect of oil to DMC ... nd the percentage conversion to FAME was obtained."
5125,10.1016/j.renene.2014.02.036,something_else,Refined soybean oil with low free fatty acid (0.06 ... ical grades and used without further purification.
5126,10.1016/j.tet.2007.11.088,something_else,To a solution of the crude 12 in THF (0.5 mL) and  ... calcd for C27H42O2: 398.3185. Found: m/z 398.3200.
5127,10.1016/j.tet.2007.11.088,something_else,The crude product was dissolved in MeOH/NH3 (1 mL) ... calcd for C27H44O2: 400.3341. Found: m/z 400.3344.
5128,10.1016/j.tet.2007.11.088,something_else,"To a solution of 11 (6.7 mg, 0.015 mmol) in dry TH ... calcd for C29H46O3: 442.3447. Found: m/z 442.3454."
5129,10.1016/j.tet.2007.11.088,something_else,To a solution of 10 (42 mg) in CH2Cl2 (5 mL) was a ... calcd for C29H44O3: 440.3290. Found: m/z 440.3293.
5130,10.1016/j.tet.2007.11.088,something_else,"To a solution of the crude diol, NEt3 (61 μL, 0.45 ... .50 (d, 1H, J=10 Hz), 5.56 (dd, 1H, J=1.9, 10 Hz)."
5131,10.1016/j.tet.2007.11.088,something_else,"Compound 9 (44 mg, 0.10 mmol) was dissolved in MeO ... calcd for C27H44O2: 400.3341. Found: m/z 400.3340."
5132,10.1016/j.renene.2014.02.036,something_else,The vegetable oil was initially transesterified in ... e mass spectra in the NIST mass spectral database.
5133,10.1002/jcp.25000,something_else,EpH4 cells grown in an anchorage-independent manne ... to the assay media with or without DIP for 3 days.
5134,10.1016/j.jpowsour.2005.03.042,something_else,The solutions were cast in glass and polytetrafluo ... lled water and dried at 50 degC for several hours.
5135,10.1016/j.solidstatesciences.2014.03.006,something_else,Graphite oxides were prepared from natural graphit ...  chemicals were used without further purification.
5136,10.1016/j.cemconres.2016.06.005,something_else,Thermal analysis was performed from 30 to 1000 deg ... mg of paste was tested in 90 μl alumina crucibles.
5137,10.1016/j.cemconres.2016.06.005,something_else,In situ XRD was not performed with sprayed pastes  ...  using the same test configuration as in situ XRD.
5138,10.1016/j.cemconres.2016.06.005,something_else,Evolution of temperature was measured in a semiadi ... accelerator addition and was performed for 30 min.
5139,10.1016/j.cemconres.2016.06.005,something_else,"Cement and water were mixed for 240 s, followed by ... ollow the same procedures as in hand-mixed pastes."
5140,10.1016/j.cemconres.2016.06.005,something_else,"Batches containing 30 kg of paste were necessary t ... lanetary speeds were 150 and 40 rpm, respectively."
5141,10.1016/j.cemconres.2016.06.005,something_else,References pastes were prepared by pre-mixing wate ...  avoid the influence of variations in temperature.
5142,10.1016/j.cemconres.2016.06.005,something_else,"Determined by ionic chromatography with a solution ... mL of concentrated nitric acid, according to [14]."
5143,10.1016/j.cemconres.2016.06.005,something_else,"Reference pastes are composed by cement, a water/c ... applied in tunnels executed with sprayed concrete."
5144,10.1016/j.cemconres.2016.06.005,something_else,"To evaluate the composition of aluminate hydrates  ... k, lowering ettringite contents in sprayed pastes."
5145,10.1016/j.cemconres.2016.06.005,something_else,"The composition and preparation procedure of the m ...  conditions, at 20 degC and 50% relative humidity."
5146,10.1016/j.cplett.2010.03.003,something_else,"Anhydrous yttrium chloride YCl3 (99.99% pure, Aldr ... re, Aldrich) have been used as starting materials."
5147,10.1016/j.tet.2008.06.084,something_else,To a solution of CuCl (0.32 mmol) in THF (5 mL) wa ... petroleum ether/ethyl acetate as eluent to give 4.
5148,10.1016/j.tet.2008.06.084,something_else,"Under nitrogen atmosphere, CuCl (2 mmol) was added ... petroleum ether/ethyl acetate as eluent to give 4."
5149,10.1016/j.tet.2008.06.084,something_else,To a solution of CuCl (0.32 mmol) in THF (5 mL) wa ... petroleum ether/ethyl acetate as eluent to give 3.
5150,10.1016/j.tet.2008.06.084,something_else,"Under nitrogen atmosphere, CuCl (2 mmol) was added ... petroleum ether/ethyl acetate as eluent to give 3."
5151,10.1016/j.tet.2008.06.084,something_else,"To an etheral solution (20 mL) of (E)-ethyl 5,5,6, ... m ether/ethyl acetate (20:1) as eluent to give 2g."
5152,10.1016/j.tet.2008.06.084,something_else,Melting points were measured with a Temp-Melt appa ...  commercially available and were used as received.
5153,10.1016/j.tet.2008.06.084,something_else,"According to the literature5, 5a, 5b, 5c, 5d, 5e a ... ory yields. The results are summarized in Table 3."
5154,10.1016/j.cemconres.2016.06.005,something_else,Distilled water and a superplasticizer based on a  ... n and pH of accelerators are presented in Table 4.
5155,10.1016/j.tet.2008.06.084,something_else,The carbocupration reaction of alkynes is an effec ... carbanion intermediate formed during the reaction.
5156,10.1016/0008-8846(81)90062-4,something_else,La spectroscopie infrarouge a basse temperature a  ... e l'etendue et de la nature de la solution solide.
5157,10.1016/j.tetlet.2006.03.054,something_else,"Aldehyde 4a and ketone 4d are commercially availab ... emie AG and Aldrich-Chemical Co Ltd, respectively."
5158,10.1016/j.cej.2007.11.017,something_else,The soil burial degradation test of segmented poly ...  vacuum at 30 degC and weighed to constant weight.
5159,10.1016/j.cej.2007.11.017,something_else,Poly(ester urethane)s films (10 mm x 10 mm and thi ... ss in blank experiment from the total weight loss.
5160,10.1016/j.cej.2007.11.017,something_else,Poly(ester urethane)s film samples (10 mm x 10 mm  ... on was quantified as the weight loss of samples as
5161,10.1016/j.cej.2007.11.017,something_else,The solubility of the poly(ester urethane)s was pe ... f dissolved polymer the solubility was determined.
5162,10.1016/j.cej.2007.11.017,something_else,The synthesis of polyurethane without soft segment ...  other conditions are the same as described above.
5163,10.1016/j.cej.2007.11.017,something_else,Segmented poly(ester urethane)s were synthesized v ... es and dried in a vacuum oven at 65 degC for 24 h.
5164,10.1016/j.cej.2007.11.017,something_else,"1,3-Propanediol (1,3-PDO, 98%), sebacic acid (99%) ... ere used as received without further purification."
5165,10.1016/j.cmet.2015.08.007,something_else,Immunoblots were performed as previously described ... s from three biological replicates per experiment.
5166,10.1016/j.tetlet.2006.03.054,something_else,"Therefore, aldehyde 4b was condensed with malonodi ... acid, gave dimethyl derivative 4c in good yield.15"
5167,10.1016/j.cmet.2015.08.007,something_else,GC-MS and SITA experiments were conducted as previ ... raphs correspond to one representative experiment.
5168,10.1016/j.tube.2011.06.007,something_else,"Mtb strains were grown to mid-log phase, a 10-fold ... lates containing OADC with or without 0.0085% SDS."
5169,10.1016/j.tube.2011.06.007,something_else,All Mtb strains were transformed with a pH-sensiti ... rting to pHIB in reference to a calibration curve.
5170,10.1016/j.tube.2011.06.007,something_else,Mtb cultures were grown in 7H9 medium to an optica ... ers for sigA and Rv2136c (Biosearch Technologies).
5171,10.1016/j.tube.2011.06.007,something_else,"All strains were cultivated in Middlebrook broth 7 ... tegration, and a streptomycin resistance cassette."
5172,10.1016/j.electacta.2007.02.023,something_else,"Inks were prepared using 20 wt% Pt/C, the Ru modif ... or to all studies to ensure a fully flooded state."
5173,10.1016/j.electacta.2007.02.023,something_else,"The synthesis of the 1.5 monolayer Ru on Pt/C cata ... 4 monolayers, based on the initial 40% dispersion."
5174,10.1016/j.tetlet.2006.03.054,something_else,General procedure for the preparation of aminonitr ... ystals through recrystallization from cyclohexane.
5175,10.1016/j.tetlet.2006.03.054,something_else,"General procedure for the preparation of diarylalk ... roleum ether (bp 60-90 degC)-ethyl acetate, 25:1)."
5176,10.1016/j.cmet.2015.08.007,something_else,"67NR, 66cl4, and 4T1 cell lines were cultured as p ... P retroviral vector system (Dickins et al., 2005)."
5177,10.1016/j.solidstatesciences.2014.03.006,something_else,"Pt/graphene nanocomposites were synthesized via fa ... , fast, and scalable microwave irradiation method."
5178,10.1002/anie.200503477,something_else,A typical procedure for the enantioselective aza-e ...  (Ar=Ph) in 82 % yield (95 % ee) as a white solid.
5179,10.1111/j.1365-2672.2007.03350.x,something_else,"Biotin-labelled PCR products, including positive a ... ion, and the hybridization patterns were recorded."
5180,10.1007/s11661-011-0731-y,something_else,"To observe the microstructures, the samples are me ...  recorded both with strain gages and extensometer."
5181,10.1002/adem.201500488,something_else,"After HPT processing, the disks were ground and me ...  near the free surfaces of the compressed samples."
5182,10.1016/0040-6090(83)90120-7,something_else,"Films of TiC, TiN and their composite were prepare ... pplying bias potentials to the substrate material."
5183,10.1016/j.matlet.2007.03.046,something_else,"The enzymes could not be removed from the catalyst ... LP is, indeed, entrapped during sol-gel formation."
5184,10.1016/j.matlet.2007.03.046,something_else,"The activity of an immobilized ALP was measured in ... ped ALP, was not able to catalyze PNPP hydrolysis."
5185,10.1016/j.matlet.2007.03.046,something_else,The assay mixture usually contained 0.02 units ALP ... tated in the legends to Table 1 and Figs. 1 and 2.
5186,10.1016/j.matlet.2007.03.046,something_else,The immobilized enzyme was packed in a column (1 m ... d between the two preparations of immobilized ALP.
5187,10.1016/j.susc.2011.11.009,something_else,TiO2 films with thickness between 10 and 260 nm we ...  storage and again after 30 min of UV irradiation.
5188,10.1007/s11661-011-0731-y,something_else,The optimization of this treatment is carried out  ...  cooling rate on the nature of the phases present.
5189,10.1016/j.jeurceramsoc.2010.11.006,something_else,A schematic drawing and a photo of a sample are sh ... mages taken with an optical polarizing microscope.
5190,10.1016/j.msea.2017.05.047,something_else,The AA-7050 wrought samples were originally purcha ... ndition according to the ASM-4201B-T7651 standard.
5191,10.1016/j.msea.2017.05.047,something_else,Thin-foil specimens for TEM studies were prepared  ... tate phases are assumed to be spherical particles.
5192,10.1016/j.matlet.2006.06.063,something_else,The consequent reaction to prepare lamellar hybrid ... elp remove the unreacted surfactant in the hybrid.
5193,10.1016/j.matlet.2006.06.063,something_else,Preparation of OCAP-POSS was according to the publ ... indicates the regular microstructure of OCAP-POSS.
5194,10.1016/j.tsf.2005.04.121,something_else,"Silicon substrate surface etched by hydrogen chlor ... n and (b) 1273 K with 1% for 75 min, respectively."
5195,10.1016/j.tsf.2005.04.121,something_else,"removing the native oxide and the organic contamin ... y baking for 10 min at 1373 K in ambient hydrogen,"
5196,10.1016/j.tsf.2005.04.121,something_else,Horizontal cold wall chemical vapor deposition rea ... g the gaseous chemical species in the exhaust gas.
5197,10.1016/j.solidstatesciences.2014.03.006,something_else,Quantum yields for hydrogen evolution by Pt/graphene and P-25 with Na2S/Na2SO3 aqueous solution.
5198,10.1016/j.msea.2017.05.047,something_else,The machined tensile specimens of the original AA- ... bation period of 96 hours at ambient temperature).
5199,10.1002/anie.200503477,something_else,"[a] Unless otherwise noted, all reactions were car ... 40:1 (S/C=200:1). [e] Reaction performed for 12 h."
5200,10.1016/j.bios.2015.02.034,something_else,"Methyl methacrylate (MMA), methacrylic acid (MAA), ... rchased from Friedemann Schmidt Chemical, Germany."
5201,10.1016/j.bios.2015.02.034,something_else,"Four different compositions of poly(MMA-co-MAA) we ... n vacuum oven at 40 degC (Hosseini et al., 2014a)."
5202,10.1111/j.1365-2672.2007.03350.x,something_else,Genomic DNA of clinical isolates was extracted as  ... f positive control and absent in negative control.
5203,10.1111/j.1365-2672.2007.03350.x,something_else,"Oligonucleotide probes (purchased from TaKaRa, Dal ...  water and air-dried for immediate use or storage."
5204,10.1016/j.actamat.2016.10.060,something_else,Aluminum alloy 5456-H116 (5%Mg) was supplied by Al ... ) orientation imaging as described in Section 2.2.
5205,10.1007/s10800-013-0653-z,something_else,"Electrochemical characterization was performed by  ... ctrodes were purchased from INESA Instrument, Inc."
5206,10.1007/s10854-011-0462-2,something_else,"Transparent conducting multilayered undoped and Sn ... ne were used as solvent and reagent, respectively."
5207,10.1016/j.mseb.2010.05.001,something_else,"Titanium-coated Corning(tm) glass substrates were  ... (O-s-Bu)3 ratios were 0.11 and 0.25, respectively."
5208,10.1016/j.mseb.2010.05.001,something_else,"Semiconductor photocatalysis with a primary focus  ... ther applications [1], [2], [3], [4], [5] and [6]."
5209,10.1016/j.mseb.2010.05.001,something_else,"In this work the study of band gap is based on the ... er energy region, leading to a band gap reduction."
5210,10.1016/j.bios.2015.02.034,something_else,"PHB fiber membranes were fabricated by electrospin ... f 6 mm (Scheme 1, center) for further experiments."
5211,10.1016/j.jeurceramsoc.2010.12.002,something_else,A fixed amount of quartz (10 wt% of the dry body w ... tals was controlled by their chemical environment.
5212,10.1016/j.jeurceramsoc.2010.12.002,something_else,"Mineralogical composition of the stoneware bodies, ... nt from those defined by the design (see Table 4)."
5213,10.1016/j.jeurceramsoc.2010.12.002,something_else,The functional surface staining of fired samples w ...  is calculated according to the following formula:
5214,10.1016/j.jeurceramsoc.2010.12.002,something_else,"X-ray powder diffraction (XRPD) data were collecte ... equently, the glass content could be calculated.30"
5215,10.1016/j.bios.2015.02.034,something_else,Among different protocols for performing ELISA suc ...  in comparison to the total number of the samples.
5216,10.1016/j.bios.2015.02.034,something_else,Polymer coated PHB fibers of all compositions were ... ELISA in 96 well-plate has been conducted as well.
5217,10.1016/j.bios.2015.02.034,something_else,The qualitative measurement of surface -COOH can b ...  concentration of -COOH expressed in μM/mm2 (n=5).
5218,10.1016/j.bios.2015.02.034,something_else,Water contact angle (WCA) measurement was carried  ... bserved for almost all of the measurements (n=15).
5219,10.1016/j.bios.2015.02.034,something_else,Polymer coatings were prepared on fabricated PHB f ... r 3 s of dipping and dried in ambient temperature.
5220,10.1016/j.jeurceramsoc.2010.12.002,something_else,"The wt% quartz in the dried body, calculated based ... the dried body so a direct comparison is possible."
5221,10.1002/jcp.25000,something_else,Total RNA was extracted from cells or tissues with ... or tubulin was determined using the 2-ΔΔCt method.
5222,10.1002/jcp.25000,something_else,"Frozen sections of mammary gland tissue and cultur ... cence microscope, BZ-X700 (Keyence, Osaka, Japan)."
5223,10.1002/jcp.25000,something_else,"Mammary gland tissue (75 mg per antibody) were fix ...  DocTM. (Bio-Rad Laboratories, Inc., Hercules, CA)"
5224,10.1016/j.solener.2010.09.007,something_else,jV-characteristics of grid cells in the dark (left ... 120 min) and subsequent annealing (3rd annealing).
5225,10.1016/j.solener.2010.09.007,something_else,Absorption spectra on films which had been exposed ...  degC under nitrogen for 5 min and measured again.
5226,10.1016/j.solener.2010.09.007,something_else,"For the impedance experiments the sample was mount ... itrogen gas to dry synthetic air (80% N2, 20% O2)."
5227,10.1016/j.solener.2010.09.007,something_else,"For manufacturing the semitransparent cells, an in ... d in more detail elsewhere (Waldauf et al., 2006)."
5228,10.1016/j.jeurceramsoc.2010.11.004,something_else,The porosity of the coated gelatin samples was det ... ng porosity of the coated ceramics was calculated.
5229,10.1016/j.jeurceramsoc.2010.11.004,something_else,After the gelatin coating all samples were allowed ... acuum or (ii) 100 degC under atmospheric pressure.
5230,10.1016/j.jeurceramsoc.2010.11.004,something_else,In order to improve the impregnation the ceramics  ... is led to an improved removal of air out of pores.
5231,10.1016/j.jeurceramsoc.2010.11.004,something_else,Before coating the open porous HA-ceramics with ge ...  centrifuge - now to remove excessive gelatin sol.
5232,10.1016/j.solener.2010.09.007,something_else,CELIV traces (smoothed by averaging over five adja ... rements were performed in the dark under nitrogen.
5233,10.1016/j.jeurceramsoc.2010.11.004,something_else,Viscosity of the gelatin sols was measured with a  ...  them at a designated temperature of 50 +- 1 degC.
5234,10.1016/j.jeurceramsoc.2010.11.004,something_else,Ballmilling this mixture for 6 min leads to the fo ... ith a height of ~3.3 cm and a diameter of ~1.9 cm.
5235,10.1016/j.jeurceramsoc.2010.11.004,something_else,"HA-powder (brand name Ostim, Aap Biomaterials, Ger ... y), as well as (iv) a sintering aid (CaNa4(PO3)6)."
5236,10.1016/j.jpowsour.2016.02.063,something_else,Linear sweep voltammograms and rotating ring-disk  ... o 0.18 V versus an RHE at a scan rate of 5 mV s-1.
5237,10.1016/j.jpowsour.2016.02.063,something_else,"Prior to the dip-coating process, commercial Ti me ... 85 degC for 24 h and calcined at 200 degC for 2 h."
5238,10.1016/j.jpowsour.2016.02.063,something_else,The ORR electrode included a catalyst layer (on th ... es were then dried in an oven at 85 degC for 24 h.
5239,10.1016/j.jpowsour.2016.02.063,something_else,"XC-72 carbon black (Vulcan XC-72, Cabot Corp., USA ... he experiments were conducted at room temperature."
5240,10.1016/j.ijhydene.2015.01.028,something_else,The supplying water (H2O) for the reaction must be ... required by this process can be expressed as [18]:
5241,10.1016/j.jeurceramsoc.2010.11.004,something_else,"Porcine gelatin granules (0.5 <= d <= 1.2 mm) type ... in this work in g gelatin per g water, i.e. ""g/g""."
5242,10.1016/j.ijhydene.2015.01.028,something_else,The schematic diagram of the photovoltaic-driven e ... er will be further heated by the heat exchanger 1.
5243,10.1016/j.icheatmasstransfer.2015.07.002,something_else,The present study developed a heat sink optimizati ... han that of the original LED module (7.154 W/m2k).
5244,10.1016/j.jhazmat.2011.01.050,something_else,"Typically, 20 mg MWCNTs were added to 10 ml aqueou ... s-500, Ag/MWCNTs-600, Ag/MWCNTs-800, respectively."
5245,10.1002/pola.24565,something_else,The Mn of PFO increased once 18-crown-6 was used a ... ained PFO reached 32.4 kg/mol with a yield of 98%.
5246,10.1002/pola.24565,something_else,Anionic polymerization of FO was carried out in an ... te)] methane (1010) was added as an antioxidant.22
5247,10.1002/pola.24565,something_else,To a 5000-mL three-necked flask equipped with a me ...  a vacuum line at room temperature for future use.
5248,10.1002/pola.24565,something_else,"Potassium tert-butoxide with 97% purity, 18-crown- ... urity were provided by Acros and used as received."
5249,10.1002/pola.24565,something_else,"2-Furyloxirane (FO), a monomer usually obtained fr ... odicals, Inc. J Polym Sci Part A: Polym Chem, 2011"
5250,10.1016/j.jpowsour.2015.12.054,something_else,Thin film depositions were carried out in a cluste ... ith a closed shutter and a ramp rate of 3 K min-1.
5251,10.1002/cbin.10466,something_else,BrdU incorporation into embryonic chicken muscles  ... (*) represents statistically different (P < 0.05).
5252,10.1002/cbin.10466,something_else,"The myoblasts were lysed in RIPA buffer supplement ... ped by enhanced chemiluminescence (Amersham, USA)."
5253,10.1002/cbin.10466,something_else,Total RNAs from the cultured cells and the skeleta ... mer sequences are listed in Supplementary Table 1.
5254,10.1002/cbin.10466,something_else,"For BrdU incorporation into embryonic muscles, egg ... ted muscle sections were calculated in this study."
5255,10.1002/cbin.10466,something_else,"Injections were made directly into the albumen of  ... ured with a digital camera (DS-Fi1, Nikon, Japan)."
5256,10.1002/cbin.10466,something_else,"After a primary culture for 2 days, myoblasts were ... posed no significant effect on cell proliferation."
5257,10.1002/cbin.10466,something_else,"The cultured myoblasts were rinsed with PBS for th ... icroscopy (Zeiss LSM 700, Carl Zeiss AG, Germany)."
5258,10.1002/cbin.10466,something_else,Muscle myoblast cells were isolated from the leg s ... nd cells were passed when they were sub-confluent.
5259,10.1002/cbin.10466,something_else,All animal experiments were approved by the Animal ... ogen and stored at -80degC until further analysis.
5260,10.1016/j.jhazmat.2011.01.050,something_else,The above experimental results demonstrate that Ag ... y. Ag/MWCNTs nanocomposites are formed ultimately.
5261,10.1016/j.jhazmat.2011.01.050,something_else,Bactericidal activity of Ag/MWCNT nanocomposites w ... erformed to investigate the effect of solar light.
5262,10.1002/cbin.10466,something_else,"For immunofluorescence staining, muscles (pectoral ... unted and images were acquired as described above."
5263,10.1016/j.cej.2011.06.079,precipitation_ceramic_synthesis,The magnetic Fe3O4 particles were prepared by copr ... ained materials were dried in an oven at 100 degC.
5264,10.1016/j.actbio.2013.02.014,precipitation_ceramic_synthesis,CS powders were prepared by a chemical coprecipita ... n particles between 100 and 150 μm for future use.
5265,10.1016/j.apsusc.2016.01.137,precipitation_ceramic_synthesis,"Hydrophobic Fe3O4 magnetic nanoparticles were prep ... mes, finally dried in an oven at 60 degC for 12 h."
5266,10.1016/j.jssc.2014.04.015,precipitation_ceramic_synthesis,CA was intercalated into Zn/Al-NO3 via the co-prec ... in an oven at 60 degC. The product was named CZAC.
5267,10.1016/j.cej.2015.08.027,precipitation_ceramic_synthesis,The ZrO2 support was prepared by a co-precipitatio ... 383 K and calcined at 773 K in static air for 3 h.
5268,10.1016/j.cattod.2011.08.040,precipitation_ceramic_synthesis,A MgO-ZrO2 support material (5:2 mole ratio) was p ... calcined MgO-ZrO2 material was designated as M5Z2.
5269,10.1016/j.powtec.2014.10.022,precipitation_ceramic_synthesis,Maghemite nanoparticles (MNPs) were prepared by co ... ield and dispersed in 40 mL ethanol for later use.
5270,10.1016/j.desal.2010.02.003,precipitation_ceramic_synthesis,Zn-Al-Cl LDH was prepared by the co-precipitation  ... (50 degC-400 degC) in nitrogen atmosphere for 8 h.
5271,10.1007/s10854-015-3897-z,precipitation_ceramic_synthesis,The AC/MnO2 composites were obtained by a chemical ... posite was dried under vacuum at 60 degC for 24 h.
5272,10.1016/j.molcata.2014.06.032,precipitation_ceramic_synthesis,CZA1 was prepared by the conventional coprecipitat ... 600 degC in air for 3 h to get the final material.
5273,10.1016/j.mseb.2007.02.009,precipitation_ceramic_synthesis,"ZnWO4 were prepared through calcination co-precipi ... 0 degC for 1 h, 2 h, 4 h, 8 h, 16 h, respectively."
5274,10.1016/j.jallcom.2015.08.016,precipitation_ceramic_synthesis,CoFe2O4 nano-particles were prepared by a facile c ... vacuum at 80 degC for 12 h to obtain nano CoFe2O4.
5275,10.1007/s10853-011-5256-7,precipitation_ceramic_synthesis,"Ce1-xFexO2 (x = 0-0.5, atomic percent) composite o ... re prepared by similar procedures described above."
5276,10.1016/j.jssc.2014.09.001,precipitation_ceramic_synthesis,PA was intercalated into Zn/Al-NO3 (R=2) via the c ... 60 degC. The resultant material was labelled PZAC.
5277,10.1016/j.electacta.2012.03.077,precipitation_ceramic_synthesis,The Fe3O4-GO nanocomposites were prepared by the c ... nd dried under vacuum at room temperature finally.
5278,10.1016/j.jhazmat.2010.08.096,precipitation_ceramic_synthesis,"As a comparison, another type of MgFe2O4 was prepa ... ed at 600 degC for 4 h, and labeled as MgFe2O4-CP."
5279,10.1016/j.fuel.2011.08.014,precipitation_ceramic_synthesis,CeCuTi and CeTi complex oxides were prepared by th ... xides were designated as CET and CCT respectively.
5280,10.1016/j.jcis.2009.02.068,precipitation_ceramic_synthesis,Fe3O4 nanoparticles were synthesized using a co-pr ... 60 degC. A black fine powder (Fe3O4) was obtained.
5281,10.1016/j.matlet.2015.03.148,precipitation_ceramic_synthesis,Lithium-doped ZnO nanopetals were synthesized usin ... h and finally calcined at 500 degC in air for 2 h.
5282,10.1016/j.apcata.2005.10.012,precipitation_ceramic_synthesis,Pd/ZnO catalysts with different Pd loadings were p ... ed by CP method with 10 wt.% Pd was labelled CP10.
5283,10.1007/s10854-015-3620-0,precipitation_ceramic_synthesis,The Mn doped SnO2 nanocrystalline materials were p ... d into fine powder to get tin oxide nanomaterials.
5284,10.1016/j.aca.2015.05.029,precipitation_ceramic_synthesis,The sorbent was synthesized by a co-precipitation  ... ct (ca. 5 g) could be stably stored for later use.
5285,10.1016/j.apcatb.2003.09.006,precipitation_ceramic_synthesis,CuFe2O4 was prepared by co-precipitation method. 0 ... s crushed and then calcinated at 300 degC for 1 h.
5286,10.1016/j.molcata.2014.08.028,precipitation_ceramic_synthesis,CuFe2O4 was prepared by chemical co-precipitation  ...  CuFe2O4 was annealed in a muffle furnace for 8 h.
5287,10.1016/j.cattod.2011.12.025,precipitation_ceramic_synthesis,"The CeO2 nanofibres were synthesized by means of t ... emperatures i.e., 300 and 600 degC for 5 h in air."
5288,10.1007/s10008-015-3097-z,precipitation_ceramic_synthesis,"Fe3O4 nanoparticles were prepared using co-precipi ... led water, then dried in a vacuum oven at 50 degC."
5289,10.1007/s10853-013-7208-x,precipitation_ceramic_synthesis,Fe3O4 magnetic nanoparticles (MNPs) were prepared  ... inally dried in a vacuum oven at 70 degC for 48 h.
5290,10.1016/j.jpowsour.2016.07.062,precipitation_ceramic_synthesis,"For comparison, pure LDH was prepared via a coprec ...  dried in a vacuum oven at 60 degC to get the LDH."
5291,10.1016/j.cej.2011.08.041,precipitation_ceramic_synthesis,NiFe2O4 was synthesized using chemical co-precipit ... he size of the prepared NiFe2O4 powder was 400 nm.
5292,10.1016/j.apcata.2010.10.032,precipitation_ceramic_synthesis,The Fe-Mo catalysts used in this study were prepar ... lyst precursors were calcined at 500 degC for 5 h.
5293,10.1016/j.spmi.2014.07.040,precipitation_ceramic_synthesis,The Fe3O4 nanoparticles were prepared by the contr ... d chemicals and dried in a vacuum oven at 70 degC.
5294,10.1016/j.cattod.2009.02.032,precipitation_ceramic_synthesis,An example of HP method using (NH4)2Ce(NO3)6 as ce ... 60 degC for 12 h and calcined at 500 degC for 2 h.
5295,10.1016/j.cej.2015.04.095,precipitation_ceramic_synthesis,The Zn-Fe layered double hydroxide intercalated wi ... he product was named as Zn-Fe-LDH in this article.
5296,10.1016/j.cattod.2010.07.025,precipitation_ceramic_synthesis,"Niobiosilica NbSiOx was prepared in water by co-pr ... m at 313 K for 2 h, and calcined at 823 K for 8 h."
5297,10.1016/j.clay.2004.03.001,precipitation_ceramic_synthesis,The sample was obtained by the co-precipitation of ...  at 60 degC and finally dried at room temperature.
5298,10.1016/j.cattod.2004.06.038,precipitation_ceramic_synthesis,"TiO2-ZrO2 (atomic ratio 1:1) was prepared by co-pr ... t 110 degC for 24 h, calcined at 550 degC for 4 h."
5299,10.1016/j.ssi.2010.05.032,precipitation_ceramic_synthesis,"Using the co-precipitation method with controlled  ... washed with distilled water, and dried at 80 degC."
5300,10.1016/j.cej.2010.10.029,precipitation_ceramic_synthesis,Co3O4-CeO2-MnOx catalysts were prepared by co-prec ... ysts prepared in this way are denoted as Co-Ce-Mn.
5301,10.1016/j.electacta.2008.05.080,precipitation_ceramic_synthesis,"MnO2: MnO2 was prepared by a co-precipitation meth ...  water, and then dried in air at 60 degC for 12 h."
5302,10.1016/j.electacta.2014.02.033,precipitation_ceramic_synthesis,Hydrotalcite was synthesised by the co-precipitati ... d by heat treatment at 450 degC for 24 hours [21].
5303,10.1016/j.enconman.2014.06.039,precipitation_ceramic_synthesis,"MnO2 was synthesized by liquid co-precipitation in ... oted as MO-200, MO-300, MO-400, MO-600 and MO-800."
5304,10.1016/j.jssc.2013.04.028,precipitation_ceramic_synthesis,"The pristine CO3-LDHs were synthesized by a standa ... litate drying, and then dried at 60 degC for 24 h."
5305,10.1016/j.apcata.2008.10.053,precipitation_ceramic_synthesis,A homogeneous-coprecipitation method [20] was used ...  Zn0La10 according to their catalyst compositions.
5306,10.1016/j.jallcom.2010.06.205,precipitation_ceramic_synthesis,"Antimony-doped tin oxide (Sn0.9Sb0.1O2, ATO) was s ...  at 800 degC for 3 h to prepare the ATO particles."
5307,10.1016/j.electacta.2013.06.122,precipitation_ceramic_synthesis,The iron oxide was synthesized by co-precipitation ... ghly with distilled water and then dried at 373 K.
5308,10.1016/j.cej.2014.09.006,precipitation_ceramic_synthesis,A novel Fe-Mg-La adsorbent with FeIII:MgII:LaIII r ...  ground into fine powder for sequence experiments.
5309,10.1016/j.matlet.2004.10.002,precipitation_ceramic_synthesis,ZnO nanoparticles were prepared by coprecipitation ... ed at 500 degC for 2 h to get the ZnO nanocrystal.
5310,10.1016/j.apcata.2005.11.011,precipitation_ceramic_synthesis,CuO/CeO2 was prepared by co-precipitation. An aque ... egC overnight and calcination at 300 degC for 3 h.
5311,10.1016/j.cej.2014.04.105,precipitation_ceramic_synthesis,The magnetic Fe3O4/MgAl-LDH composite was prepared ... last the composite was dried at 60 degC overnight.
5312,10.1007/s10800-013-0542-5,precipitation_ceramic_synthesis,"Amorphous FePO4*2H2O was synthesized by a co-preci ... fugation, then dried in oven at 80 degC overnight."
5313,10.1002/app.30791,precipitation_ceramic_synthesis,DS-LDH was synthesized by standard coprecipitation ...  60degC for 3 days to yield a white powder DS-LDH.
5314,10.1016/j.cej.2015.12.081,precipitation_ceramic_synthesis,"HFO NPs were prepared by co-precipitation method a ... , dried at 85 degC and grounded to obtain HFO NPs."
5315,10.1016/j.mssp.2013.04.013,precipitation_ceramic_synthesis,Nanocrystalline CoFe2O4 is prepared by wet chemica ... tant dried product is powdered in an agate mortar.
5316,10.1016/j.fuel.2008.04.015,precipitation_ceramic_synthesis,Ce0.75Zr0.25O2 solid solution was prepared by the  ... ed by the method according to the above procedure.
5317,10.1016/j.actbio.2013.06.022,precipitation_ceramic_synthesis,Sodium alginate (low viscosity) and GDL were obtai ... m were obtained for future use after being sieved.
5318,10.1007/s10853-006-0981-z,precipitation_ceramic_synthesis,"For the synthesis using co-precipitation, calculat ... 0 degC and then calcined for perovskite formation."
5319,10.1016/j.cej.2014.11.059,precipitation_ceramic_synthesis,Magnetite nanoparticles were produced through co-p ... gnet and were dispersed in 500 ml deionized water.
5320,10.1016/j.cej.2011.11.006,precipitation_ceramic_synthesis,The orange peel was washed with water and dried in ...  degC for 24 h and finally stored for further use.
5321,10.1016/j.fuel.2015.09.082,precipitation_ceramic_synthesis,"For comparison, the Cu/ZnO/Al2O3 catalyst (CZA-CC) ... 12 h, followed by calcination at 450 degC for 4 h."
5322,10.1016/j.jelechem.2012.02.007,precipitation_ceramic_synthesis,"Ni-Al LDH intercalated with CO 3 2 - (Ni-Al CO 3 2 ... washed with distilled water, and dried at 80 degC."
5323,10.1016/j.jpowsour.2005.02.030,precipitation_ceramic_synthesis,The Cu/ZnO/Al2O3 catalysts were prepared by coprec ... C and calcined under air flow for 1 h at 360 degC.
5324,10.1016/j.jssc.2004.11.005,precipitation_ceramic_synthesis,This compound was prepared with a coprecipitation  ...  washed with deionized water and dried at 60 degC.
5325,10.1016/j.jhazmat.2011.09.009,precipitation_ceramic_synthesis,The magnetite nanoparticles were prepared by the c ... llowed by drying at 80 degC under vacuum for 11 h.
5326,10.1016/j.jelechem.2016.01.001,precipitation_ceramic_synthesis,The MgO nanoflakes were synthesized by co-precipit ... r times to remove impurities present in the MgONF.
5327,10.1016/j.cej.2015.05.037,precipitation_ceramic_synthesis,Surfactant modified ZnAl-LDHs were prepared by a c ... similar method. The product was denoted as DS-LDH.
5328,10.1016/j.cattod.2007.10.085,precipitation_ceramic_synthesis,The Mg-Al LDH containing C6H5COO- anions (LDH-[C6H ... 73 K for 12 h and then LDH-[C6H5COO] was obtained.
5329,10.1016/j.electacta.2015.12.036,precipitation_ceramic_synthesis,The M(OH)2 precursor was prepared by a co-precipit ... hen was dried in vacuum oven at 120 degC for 12 h.
5330,10.1007/s10008-006-0231-y,precipitation_ceramic_synthesis,[Ni4Al(OH)10]NO3 was prepared by the co-precipitat ...  dried in vacuum at 50 degC. This is the sample 1.
5331,10.1016/j.electacta.2011.03.067,precipitation_ceramic_synthesis,Hydrotalcite was synthesised by the co-precipitati ... s obtained by heat treatment at 450 degC for 24 h.
5332,10.1016/j.ijhydene.2011.12.023,precipitation_ceramic_synthesis,The 1% (w/w) PtAu/CeO2-ZnO catalyst was prepared b ... gC for 12 h and then calcined at 500 degC for 5 h.
5333,10.1016/j.cej.2006.05.014,precipitation_ceramic_synthesis,"The compound oxide supports were prepared by copre ... egC for 2 h, then at a proper temperature for 4 h."
5334,10.1016/j.jpcs.2006.01.081,precipitation_ceramic_synthesis,The synthesis of LDHs is usually achieved using th ... nd finally dried under vacuum at room temperature.
5335,10.1016/j.renene.2016.02.068,precipitation_ceramic_synthesis,Iron (II) doped ZnO nanoparticle was synthesized b ... oparticles and further calcinated at 700 degC [6].
5336,10.1007/s10853-014-8118-2,precipitation_ceramic_synthesis,"The GOF/Fe3O4 was prepared by a simple coprecipita ... ely, then dried in a vacuum oven at 60 C for 24 h."
5337,10.1016/j.jallcom.2012.01.083,precipitation_ceramic_synthesis,"In a typical procedure, nanocrystals of Li0.5Fe2.5 ... wed by drying in an air oven at 100 degC for 36 h."
5338,10.1016/j.apcata.2004.04.038,precipitation_ceramic_synthesis,The catalyst precursor was prepared by the copreci ... ntrifugation until no chlorine ions were detected.
5339,10.1016/j.electacta.2016.11.011,precipitation_ceramic_synthesis,MAC was synthesized via a modified co-precipitatio ... he particles were washed with DI water five times.
5340,10.1016/j.mssp.2015.06.043,precipitation_ceramic_synthesis,ZnxCd1-xS solid solutions were prepared using a co ... obtained by calcination at 500 degC for 5 h in N2.
5341,10.1016/j.ab.2013.04.025,precipitation_ceramic_synthesis,PB nanoparticles were synthesized by a coprecipita ... with water several times and resuspended in water.
5342,10.1016/j.apcatb.2007.04.013,precipitation_ceramic_synthesis,The catalysts were prepared by the co-precipitatio ... except that it was calcinated at 550 degC for 2 h.
5343,10.1016/j.matlet.2013.09.111,precipitation_ceramic_synthesis,Synthesis of Fe3O4 MNPs: Fe3O4 MNPs were prepared  ... d dried by vacuum at 60 degC to obtain Fe3O4 MNPs.
5344,10.1016/j.cattod.2011.03.024,precipitation_ceramic_synthesis,"The synthesis of the CuOx/CeO2 catalyst by copreci ... 60 degC and finally, calcined at 300 degC for 2 h."
5345,10.1016/j.cej.2011.10.053,precipitation_ceramic_synthesis,Ca-Fe-LDH was synthesized by coprecipitation metho ... preparation process to minimize CO2 contamination.
5346,10.1002/jssc.201500743,precipitation_ceramic_synthesis,Fe3O4/SiO2 NPs were produced according to our prev ... everal times followed by drying at 60degC for 4 h.
5347,10.1016/j.cej.2010.08.060,precipitation_ceramic_synthesis,"All the materials were reagent grade and used with ... re obtained, named by S1, S2 and S3, respectively."
5348,10.1016/j.molcata.2012.10.019,precipitation_ceramic_synthesis,Ru/CeO2 catalyst was prepared by using co-precipit ... O2 and x was the adding amount of silver in ceria.
5349,10.1016/j.jallcom.2004.03.030,precipitation_ceramic_synthesis,(1%)Eu3+:KGdF4 (Eu:KGF) was prepared by the coprec ... then two times with methanol and dried at 50 degC.
5350,10.1016/j.jconrel.2006.11.031,precipitation_ceramic_synthesis,The co-precipitation method produced a gelatinous  ... ic acid before dispersing in biopolymer solutions.
5351,10.1016/j.chroma.2013.10.067,precipitation_ceramic_synthesis,The Fe3O4@SiO2 magnetic nanoparticles (MNPs) were  ...  were encapsulated with a mesoporous silica shell.
5352,10.1016/j.jpowsour.2011.07.052,precipitation_ceramic_synthesis,CuMC-CP was synthesized by a co-precipitation meth ... degC and then calcined at 500 degC for 2 h in air.
5353,10.1016/j.matchemphys.2015.03.056,precipitation_ceramic_synthesis,"Mn doped ZnO (0, 5, 10, 15 and 20 at %) NP's were  ... MZ5 for 0, 5, 10, 15 and 20 at % Mn doping in ZnO."
5354,10.1016/j.apcata.2006.05.002,precipitation_ceramic_synthesis,A series of CuO/CeO2 catalysts were prepared by co ... amount of CuO in the CuO/CeO2 catalyst was 40 wt%.
5355,10.1016/j.cej.2014.02.044,precipitation_ceramic_synthesis,Adsorbent: MnFe2O4 was prepared by co-precipitatio ... ared sample MnFe2O4 was calcined at 673 K for 2 h.
5356,10.1016/j.cej.2012.01.085,precipitation_ceramic_synthesis,The Fe-Al-Ce trimetal oxide powder was prepared by ... C and crushed to a fine powder with a roller mill.
5357,10.1016/j.materresbull.2015.12.028,precipitation_ceramic_synthesis,"Nanoparticles of Ni0.4Zn0.4Co0.2Fe2O4 were prepare ... ed as NZCF0, NZCF1, NZCF2, NZCF3, NZCF4 and NZCF5."
5358,10.1016/j.jpowsour.2006.09.096,precipitation_ceramic_synthesis,Catalyst supports were prepared by co-precipitatio ... s crushed and calcined in air at 800 degC for 1 h.
5359,10.1016/j.solidstatesciences.2013.04.017,precipitation_ceramic_synthesis,Ag-SnO2 nanoparticles were prepared by the co-prec ...  procedure without the addition of silver nitrate.
5360,10.1016/j.electacta.2015.10.160,precipitation_ceramic_synthesis,Carbon coated V2O5 was synthesized via co-precipit ... egC for 2 h to get carbon coated V2O5 and denoted.
5361,10.1016/j.colsurfa.2009.06.040,precipitation_ceramic_synthesis,The Mg-Al-CO3-LDHs were prepared by co-precipitati ... h distilled water and dried at 110 degC overnight.
5362,10.1016/j.cattod.2011.04.053,precipitation_ceramic_synthesis,Urea gelation co-precipitation has also been used. ... rent drying processes described for the DP method.
5363,10.1016/j.carbon.2013.07.023,precipitation_ceramic_synthesis,"The production of CuFe2O4 is similar to the co-pre ... , the sample is heated in air at 600 degC for 4 h."
5364,10.1016/j.molcata.2013.04.019,precipitation_ceramic_synthesis,Fe3O4 nanoparticles were synthesized according to  ... ol and then dried in a vacuum for 12 h at 40 degC.
5365,10.1016/j.jhazmat.2015.12.035,precipitation_ceramic_synthesis,"The precursor of Mn substituted spinel ferrite, Mn ... Mn0.5 - T, where T is the calcination temperature."
5366,10.1016/j.molcata.2013.03.003,precipitation_ceramic_synthesis,MNPs were synthesized by co-precipitation of FeCl3 ... r and then dried under vacuum at 60 degC for 12 h.
5367,10.1002/pc.22569,precipitation_ceramic_synthesis,"Iron oxide nanoparticles were prepared by a coprec ... zed water. FTIR (KBr): 3415 (m, br), 584 (s) cm-1."
5368,10.1016/j.actbio.2012.10.019,precipitation_ceramic_synthesis,Powders of the CS and β-TCP bioceramics were prepa ... tween 100 and 150 μm were obtained for future use.
5369,10.1016/j.msec.2005.09.042,precipitation_ceramic_synthesis,Cobalt ferrite nanoparticles were prepared through ... zed as described throughout the rest of the paper.
5370,10.1016/j.jcat.2004.07.010,precipitation_ceramic_synthesis,"For the coprecipitation route, 0.15 M NaHCO3 aqueo ... 450 degC for 5 h. It was named as Ce0.9Cu0.1OY-cp."
5371,10.1016/j.physe.2009.04.020,precipitation_ceramic_synthesis,"Two different CdS samples were prepared via a copr ...  time will be referred to hereafter as ""sample 1""."
5372,10.1016/j.apcatb.2006.05.006,precipitation_ceramic_synthesis,The catalysts were synthesized by the co-precipita ...  were denoted as MnCux where x was the aging time.
5373,10.1016/j.matchemphys.2016.06.040,precipitation_ceramic_synthesis,ZnFe2O4/ZnO nanoparticles were prepared by co-prec ... g) was maintained constant in all the experiments.
5374,10.1016/j.jpowsour.2012.08.093,precipitation_ceramic_synthesis,Ni-Al LDH intercalated with CO 3 2 - (Ni-Al CO 3 2 ... as prepared in the same way as Ni-Al CO 3 2 - LDH.
5375,10.1016/j.molcata.2011.05.011,precipitation_ceramic_synthesis,"In the co-precipitation with supercritical drying  ... ition in ethanol (250 degC, 7.5 MPa) subsequently."
5376,10.1016/j.matchemphys.2014.01.009,precipitation_ceramic_synthesis,"γ-Fe2O3 was prepared by coprecipitation [30], [31] ... distilled water and dried at 85 degC under vacuum."
5377,10.1016/j.ica.2015.01.014,precipitation_ceramic_synthesis,Nanocrystals of Co0.5Zn0.5Fe2O4 were prepared by c ... le would be referred as CZCP-RT in the manuscript.
5378,10.1016/j.biomaterials.2015.03.029,precipitation_ceramic_synthesis,Chemical co-precipitation method was used to obtai ... obtain CS powder with size between 100 and 150 μm.
5379,10.1016/j.matlet.2015.10.137,precipitation_ceramic_synthesis,"To prepare pure Bi2O3, 9.7 g Bi(NO3)3*5H2O was dis ... lcination at 600 degC for 4 h in a muffle furnace."
5380,10.1016/j.apcatb.2013.05.035,precipitation_ceramic_synthesis,"The cerium-niobium mixed oxides were prepared by c ... O2, were prepared by similar precipitation method."
5381,10.1016/j.apsusc.2014.02.054,precipitation_ceramic_synthesis,"Fe3O4 MNPs were synthesized by an improved copreci ... mes, and then dried in vacuum at 40 degC for 24 h."
5382,10.1016/j.cej.2011.01.006,precipitation_ceramic_synthesis,Magnetic chitosan nanoparticles were prepared by c ... particles were finally dried in vacuum at 70 degC.
5383,10.1016/j.jlumin.2012.09.014,precipitation_ceramic_synthesis,Gd2O3:Sm3+ nanoparticle was prepared using the car ... alcining the precursor powder at 800 degC for 2 h.
5384,10.1016/j.electacta.2012.07.108,precipitation_ceramic_synthesis,The FePO4*xH2O precursors were prepared by using a ...  after being dried in an oven at 80 degC for 12 h.
5385,10.1016/j.electacta.2016.03.082,precipitation_ceramic_synthesis,"When the co-precipitation solution cooled down to  ... ater and alcohol repeatedly, and dried at 50 degC."
5386,10.1016/j.cej.2011.08.020,precipitation_ceramic_synthesis,Fe3O4 nanoparticles were synthesized by co-precipi ... ant chemical reaction can be expressed as follows:
5387,10.1016/j.jpcs.2009.12.018,precipitation_ceramic_synthesis,Different NiAl-CO3 LDH samples were synthesized by ... ith deionized water and dried at room temperature.
5388,10.1016/j.cej.2012.07.010,precipitation_ceramic_synthesis,The active component PdCl2 was loaded on the suppo ...  h to obtain the catalysts of Pd/CuO-Ce0.5Mn0.5O2.
5389,10.1007/s10853-011-6003-9,precipitation_ceramic_synthesis,"The magnetic ZnAl-LDH precursor was synthesized by ... y deionized water, and dried at 70 degC overnight."
5390,10.1016/j.jallcom.2010.08.101,precipitation_ceramic_synthesis,"Ce0.67Zr0.33O2 was prepared by a coprecipitation r ...  temperature and drying temperature, respectively."
5391,10.1007/s10854-014-2296-1,precipitation_ceramic_synthesis,Sn0.94Zn0.04O2 nanoparticles were synthesized by c ... 50 degC for 4 h to obtain the final nanoparticles.
5392,10.1016/j.jcat.2015.08.013,precipitation_ceramic_synthesis,"Mg4Al2Ti1-LDH and Mg4Al2-LDH catalysts were prepar ...  pH 7 was reached, and dried at 80 degC overnight."
5393,10.1016/j.cej.2013.01.036,precipitation_ceramic_synthesis,Cobalt ferrite nanoparticles were prepared by a co ... or 5 h to form nanocrystalline CoFe2O4/TiO2 (CFT).
5394,10.1002/adfm.201400310,precipitation_ceramic_synthesis,"CoIICoIII-CO3 compound was prepared by TOR, adapti ... cipitation method as described previously.[42, 43]"
5395,10.1016/j.cattod.2005.09.018,precipitation_ceramic_synthesis,Supports and catalysts were prepared in our labora ... solid was crushed and calcined in air at 600 degC.
5396,10.1016/j.cej.2014.02.080,precipitation_ceramic_synthesis,The Fe3O4 magnetic nanoparticles were synthesized  ... ted and washed several times with deionized water.
5397,10.1016/j.solidstatesciences.2009.06.015,precipitation_ceramic_synthesis,"The ZnAl-CO3-LDH precursor with magnetic propertie ... r, and dried at 50 degC for 24 h in a vacuum oven."
5398,10.1016/j.fuel.2014.07.010,precipitation_ceramic_synthesis,"The NO3-Mg/Al was synthesized by conventional co-p ... er (~6 L), and finally dried overnight at 80 degC."
5399,10.1016/j.apcatb.2014.04.043,precipitation_ceramic_synthesis,"Magnetic Fe3O4 nanoparticles were synthesized by c ... vernight, and ground in an agate mortar for 2 min."
5400,10.1016/j.cej.2012.01.017,precipitation_ceramic_synthesis,Mixed oxides containing iron and cobalt catalysts  ... atmosphere for 6 h with a ramp rate of 3 degC/min.
5401,10.1016/j.cattod.2016.12.007,precipitation_ceramic_synthesis,Direct synthesis by co-precipitation (LEV@LDH-pp): ... ated water and dried under vacuum at 60 degC [23].
5402,10.1016/j.cej.2015.07.008,precipitation_ceramic_synthesis,The γ-Fe2O3 MNPs were obtained by a chemical co-pr ... inally dried at 60 degC in a vacuum oven for 48 h.
5403,10.1016/j.mssp.2015.05.035,precipitation_ceramic_synthesis,Fe3O4 nanoparticles were synthesized by co-precipi ... a magnet. The particles are left to dry in vacuum.
5404,10.1016/j.electacta.2015.07.182,precipitation_ceramic_synthesis,The nano-sized GDC20 powder was synthesized by (NH ...  h and the pressure was controlled at about 8 MPa.
5405,10.1016/j.electacta.2015.01.132,precipitation_ceramic_synthesis,Co2Al-ABTS LDH compound was prepared by the coprec ... the same protocol and used as a reference product.
5406,10.1016/j.jpcs.2015.08.005,precipitation_ceramic_synthesis,CoFe2O4 nanoparticles were synthesized by the co-p ... e of CoFe2O4 nanoparticles and their agglomerates.
5407,10.1016/j.electacta.2014.11.085,precipitation_ceramic_synthesis,Preparation of CAN-LDH: All chemicals used in the  ... r and ethanol for several times by centrifugation.
5408,10.1016/j.apsusc.2016.08.040,precipitation_ceramic_synthesis,Magnetic photocatalysts were prepared according to ...  washed with distilled deionized water many times.
5409,10.1016/j.poly.2015.08.020,precipitation_ceramic_synthesis,Zn-Al LDH was synthesized by a coprecipitation met ... ith deionized water and used for characterization.
5410,10.1016/j.cej.2014.05.019,precipitation_ceramic_synthesis,The ferric-based layered double hydroxide intercal ... lation was named as Mg-Fe-Ala-LDH in this article.
5411,10.1016/j.jpcs.2007.03.003,precipitation_ceramic_synthesis,The cation composition of the LDH material is Zn2A ... nized water and finally dried at room temperature.
5412,10.1016/j.colsurfb.2015.03.021,precipitation_ceramic_synthesis,Dextrin-coated ZCFNPs were synthesized by an aqueo ... he ferrite samples were dried at room temperature.
5413,10.1016/j.jpcs.2011.10.016,precipitation_ceramic_synthesis,The co-precipitation method was used to prepare Zn ... wder and stored in sample bottles for further use.
5414,10.1007/s10800-008-9637-9,precipitation_ceramic_synthesis,The CP-ZnCa active materials were prepared by a ch ... acked in a PE bag for further examination and use.
5415,10.1016/j.cej.2012.02.008,precipitation_ceramic_synthesis,CuFe2O4/sawdust magnetic composite with mass ratio ... er and dried in an oven at 105 degC [22] and [23].
5416,10.1016/j.jcat.2007.03.025,precipitation_ceramic_synthesis,Pd0.05Mg0.65Al0.3(OH)2(NO3)0.3 (designated PdMgAl- ... ut drying for the subsequent ion-exchange process.
5417,10.1016/j.conbuildmat.2013.06.049,precipitation_ceramic_synthesis,The Mg(2)Al-CO3 was synthesized by a pH-controlled ... s then dried for 16-18 h at 105 degC under vacuum.
5418,10.1016/j.jpcs.2007.03.045,precipitation_ceramic_synthesis,"LDHs can be readily synthesized by coprecipitation ... 48 h, ground and finally stored in plastic bottle."
5419,10.1016/j.cej.2012.01.109,precipitation_ceramic_synthesis,Palygorskite was impregnated with metal salts by p ... ound and sieved to obtain particles of 20-40 mesh.
5420,10.1016/j.matlet.2014.01.085,precipitation_ceramic_synthesis,"The procedure used to prepare the LDHs was based o ... s were designated HT-Mg/Al, HT-Mg/Ga and HT-Mg/In."
5421,10.1007/s10008-017-3564-9,precipitation_ceramic_synthesis,Ni0.8Co0.1Mn0.1CO3 was synthesized by a typical co ...  0.3 M of MnSO4[?]H2O to produce other precursors.
5422,10.1016/j.cej.2010.08.088,precipitation_ceramic_synthesis,"The CuOx-CeO2 catalyst was prepared by the copreci ...  at 60 degC and finally, calcined 2 h at 300 degC."
5423,10.1007/978-81-322-2773-1_21,precipitation_ceramic_synthesis,Potassium permanganate (KMnO4) and manganese sulfa ... terials and then dried at 80 degC in air for 12 h.
5424,10.1016/j.fuproc.2010.09.024,precipitation_ceramic_synthesis,NiCe-CP was obtained by co-precipitation of aqueou ... ight and calcined in flowing air at 773 K for 3 h.
5425,10.1016/j.matchemphys.2010.09.031,precipitation_ceramic_synthesis,The preparation of Fe3O4 nanoparticles was followe ... ried at room temperature under evacuated for 12 h.
5426,10.1016/j.cplett.2010.10.037,precipitation_ceramic_synthesis,Nanocrystalline powders of ZnAl2O4/Co(II) were pre ... ned at temperatures in the range of 600-1000 degC.
5427,10.1111/php.12164,precipitation_ceramic_synthesis,"ZnO-SnO2 nanoparticles were prepared by coprecipit ... ned at 400degC, 500degC, and 600degC for 3 h [15]."
5428,10.1016/j.matchemphys.2015.03.066,precipitation_ceramic_synthesis,All the chemical reagents were of analytical grade ...  degC in air for 12 h to obtain the final samples.
5429,10.1016/j.expthermflusci.2013.08.018,precipitation_ceramic_synthesis,"In the present work, co-precipitation was used to  ... en at 200 degC for 1 h yielding white TiO2 powder."
5430,10.1016/j.jssc.2004.07.024,precipitation_ceramic_synthesis,The CO3/Zn-Al LDH (CO3/LDH) was prepared by a stan ... O3/LDH was [Zn0.67Al0.33(OH)2][(CO3)0.16*0.55H2O].
5431,10.1016/j.ijhydene.2015.12.061,precipitation_ceramic_synthesis,"Ag3PO4 was synthetized by coprecipitation method i ...  calcination temperature (200, 300, 400, and 500)."
5432,10.1016/j.apcatb.2010.03.022,precipitation_ceramic_synthesis,Ce0.67Zr0.33O2 doped by nickel oxide with differen ...  1000 degC for 4 h in air to obtain aged supports.
5433,10.1016/j.jallcom.2016.06.227,precipitation_ceramic_synthesis,A low saturation coprecipitation method was employ ... e increase rate of 5 degC/min and furnace cooling.
5434,10.1007/s10854-014-1910-6,precipitation_ceramic_synthesis,Fe3O4 NPs were obtained via a facile coprecipitati ...  an electric vacuum oven at 60 degC for 12 h [35].
5435,10.1016/j.apcatb.2015.04.038,precipitation_ceramic_synthesis,"As a comparison, NiCo2O4-CP was also synthesized b ... illed water and then calcined at 400 degC for 3 h."
5436,10.1016/j.materresbull.2005.03.021,precipitation_ceramic_synthesis,"In the co-precipitation method, the starting mater ... in the amount of BaCl2 and TiOCl2 solutions taken."
5437,10.1016/j.jpowsour.2007.04.091,precipitation_ceramic_synthesis,"All chemicals are AR grade and used as received. T ... cuum at 80 degC for 2 h, denoted as Co-Al LDH(OH)."
5438,10.1016/j.mseb.2004.01.024,precipitation_ceramic_synthesis,"The powder of Cd2Sb2O7 was prepared by co-precipit ...  of powder was measured by SEM (Hitachi, S-2460N)."
5439,10.1016/j.apcata.2007.07.034,precipitation_ceramic_synthesis,"The CuO-CeO2 catalyst was prepared by co-precipita ... atomic absorption spectroscopy (AAS), was 5.0 wt%."
5440,10.1016/j.jmmm.2013.12.033,precipitation_ceramic_synthesis,"The CoFe2O4 nano-particles were prepared using the ... n, the precipitate was dried at 110 degC for 12 h."
5441,10.1007/s10008-014-2701-y,precipitation_ceramic_synthesis,LDH has been synthesized by co-precipitation of Mg ... n gas flow and using decarbonated-deionized water.
5442,10.1016/j.matchemphys.2009.09.001,precipitation_ceramic_synthesis,The chloride-intercalated Zn-Cr-LDH sample (ZnCr0) ... ral times with water and finally dried at 60 degC.
5443,10.1016/j.biortech.2011.03.039,precipitation_ceramic_synthesis,MgZnAlO modified catalyst was prepared by co-preci ...  - xZn1 + xAl(2 - y)/3O3 i.e. 0.1 x 0.9 and y = 0.
5444,10.1016/j.apcatb.2011.01.008,precipitation_ceramic_synthesis,The Mn0.6Ce0.4O2 mixed oxide was prepared by a mod ... 3 K for 12 h and calcined at 723 K for 6 h in air.
5445,10.1016/j.jpowsour.2016.03.003,precipitation_ceramic_synthesis,FePO4 nanoparticles were synthesized by means of c ... gents that were used without further purification.
5446,10.1016/j.jpowsour.2015.03.067,precipitation_ceramic_synthesis,NiFe2O4 was prepared by a conventional co-precipit ... lcinated at 475 degC for 4 h under air atmosphere.
5447,10.1016/j.jssc.2016.08.019,precipitation_ceramic_synthesis,Zinc hydroxide nitrate (ZnHN) was synthesized by t ... The white solid was dried at 65 degC for two days.
5448,10.1002/cssc.201403060,precipitation_ceramic_synthesis,The FePO4/PAA nanoparticles were prepared by copre ... in air for 24 h to obtain FePO4/PAA nanoparticles.
5449,10.1016/j.cej.2016.01.041,precipitation_ceramic_synthesis,The organic LDH was also prepared by the co-precip ... sis processes of Ni-Cr LDHs was shown in Scheme 1.
5450,10.1016/j.apcata.2006.05.013,precipitation_ceramic_synthesis,"Several Ni/MgO catalysts, containing 1, 5, 10 and  ...  flow rate H2 (99.99% purity) at 500 degC for 6 h."
5451,10.1016/j.fuproc.2010.12.015,precipitation_ceramic_synthesis,"The Zn-Al LDH was prepared by co-precipitation of  ... ter, the products were dried at 100 degC for 12 h."
5452,10.1002/adsc.201300551,precipitation_ceramic_synthesis,CoFe2O4 NPs were prepared by a chemical co-precipi ... hanol and drying at 100 degC in a vacuum for 24 h.
5453,10.1016/j.jcat.2011.07.001,precipitation_ceramic_synthesis,A CeO2-Ag catalyst was synthesized by a coprecipit ...  the catalyst preparation is given elsewhere [28].
5454,10.1016/j.molcata.2006.11.036,precipitation_ceramic_synthesis,Sample 1 (designated as 5CuC-CP) was synthesized b ... e was thermally treated at 500 degC for about 2 h.
5455,10.1016/j.matchemphys.2007.07.018,precipitation_ceramic_synthesis,"The Zn2Al-LDH/CA, Zn2Al-LDH/DMOCA and Zn2Al-LDH/PH ...  decarbonated water and dried at 50 degC for 30 h."
5456,10.1016/j.electacta.2016.01.201,precipitation_ceramic_synthesis,CoAl-LDHs were synthesized by a coprecipitation me ... inally dried at 60 degC for 12 h in a vacuum oven.
5457,10.1016/j.porgcoat.2012.04.006,precipitation_ceramic_synthesis,The co-precipitation method was applied for the pr ...  powders were calcined in air at 800 degC for 2 h.
5458,10.1016/j.jcis.2015.05.009,precipitation_ceramic_synthesis,"All chemicals were of analytical purity, which wer ... ter as M-10-400, M-10-600, M-10-800 and M-10-1000."
5459,10.1007/s10854-015-3031-2,precipitation_ceramic_synthesis,"Cobalt substituted cadmium ferrite (Cd0.9Co0.1Fe2O ... or 2 h. Hereafter, the samples named as S1 and S2."
5460,10.1016/j.apsusc.2013.06.087,precipitation_ceramic_synthesis,The ZMAC-LDHs were synthesized by coprecipitation  ...  until pH reached 7 and dried at 80 degC for 12 h.
5461,10.1016/j.matchemphys.2012.05.007,precipitation_ceramic_synthesis,"For comparative studies, conventional YVO4:Eu3+ wa ... ltered and then heated at 700 degC in air for 4 h."
5462,10.1016/j.cej.2015.05.110,precipitation_ceramic_synthesis,Step 1: Magnetic chitosan particles were prepared  ... mediary product was called MC (magnetic chitosan).
5463,10.1016/j.jpcs.2007.10.132,precipitation_ceramic_synthesis,The LiAl LDH-NO3- was prepared by co-precipitation ...  de-ionized water and dried under vacuum for 24 h.
5464,10.1016/j.mssp.2014.12.053,precipitation_ceramic_synthesis,The zinc oxide nanoparticles were biosynthesized b ... purified precipitate at 60 degC in oven overnight.
5465,10.1016/j.jeurceramsoc.2003.09.023,precipitation_ceramic_synthesis,"An oxalate coprecipitation method was used to prep ... e in ethanol, finally dried at ~100 degC for 20 h."
5466,10.1016/j.matchemphys.2015.08.041,precipitation_ceramic_synthesis,In the present paper maghemite nanoparticles are s ... tmosphere with an annealing rate of 5 degC/minute.
5467,10.1016/j.jssc.2010.09.036,precipitation_ceramic_synthesis,"[Ca2Al(OH)6]NO3*yH2O (Ca2Al-NO3) was prepared usin ...  filtration, washed, and dried as described above."
5468,10.1016/j.jpcs.2008.09.007,precipitation_ceramic_synthesis,The precursor was prepared by a co-precipitation m ... l2O3 was not reduced to Al by H2 at 700-800 degC).
5469,10.1007/s10854-015-3250-6,precipitation_ceramic_synthesis,Synthesis of chromium doped strontium hexaferrites ... d pellets were used for further characterizations.
5470,10.1016/j.apcatb.2015.03.004,precipitation_ceramic_synthesis,Au/CeO2 (AuCe) and Au/Fe2O3 (AuFe) samples were al ... t 80 degC and calcined in air at 400 degC for 2 h.
5471,10.1016/j.jpcs.2003.08.034,precipitation_ceramic_synthesis,The Mg-Al-LDH (MII/MIII=2) intercalated with carbo ...  solid was dried under vacuum at room temperature.
5472,10.1007/s10854-014-1841-2,precipitation_ceramic_synthesis,Undoped and Zn-doped SnO2 powders were synthesized ... und in very good agreement with the nominal value.
5473,10.1016/j.ijhydene.2013.12.002,precipitation_ceramic_synthesis,"The 0.5, 1.0, 2.0 and 5.0 wt% CuO-ZnO supports, we ... f ZnO without CuO was prepared by the same method."
5474,10.1016/j.apsusc.2006.06.028,precipitation_ceramic_synthesis,A series of CuO/CeO2 catalysts were prepared by co ... 0 degC overnight and calcined at 500 degC for 4 h.
5475,10.1016/j.cej.2010.02.013,precipitation_ceramic_synthesis,"MnFe2O4 magnetic nanoparticles were prepared by th ... ticles with Co(NO3)26H2O, FeCl36H2O and FeCl24H2O."
5476,10.1016/j.fuel.2013.07.095,precipitation_ceramic_synthesis,MgAl2O4 support was prepared by using co-precipita ... 0 h with 5 degC/min heating rate under static air.
5477,10.1007/s10853-015-9377-2,precipitation_ceramic_synthesis,"In order to increase the ionization rate of H2WO4, ... ere dried in a lab oven at 60 degC for some hours."
5478,10.1016/j.nanoen.2017.04.005,precipitation_ceramic_synthesis,LLO nanoplates were synthesized by a solid-state r ...  in air under the same conditions described above.
5479,10.1016/j.apcata.2009.09.017,precipitation_ceramic_synthesis,The catalysts were prepared by a co-precipitation  ... compositions of the samples are listed in Table 1.
5480,10.1016/j.apenergy.2010.12.057,precipitation_ceramic_synthesis,Mg-Zr solid base catalyst with Mg-Zr mass ratio of ...  degC for 4 h to obtain Mg-Zr solid base catalyst.
5481,10.1007/s10853-014-8498-3,precipitation_ceramic_synthesis,The functionalization of Al2Mo3O12 was carried out ... t VTMS was grafted onto the nanoparticle surfaces.
5482,10.1007/s10562-008-9450-4,precipitation_ceramic_synthesis,γ-Bi2MoO6 catalyst was prepared by a co-precipitat ...  in an air stream to yield the γ-Bi2MoO6 catalyst.
5483,10.1016/j.matchemphys.2009.12.010,precipitation_ceramic_synthesis,"A typical chemical co-precipitation technique was  ...  for 12 h, powdered and calcined at 773 K for 6 h."
5484,10.1016/j.ssi.2005.02.023,precipitation_ceramic_synthesis,The precursor Ni0.6Co0.2Mn0.2(OH)2 was prepared by ... and finally calcined in air at higher temperature.
5485,10.1016/j.apcata.2009.02.036,precipitation_ceramic_synthesis,The samples were prepared by a co-precipitation me ... d in an air flow at 800 degC for 6 h to obtain NA.
5486,10.1016/j.jcat.2008.04.017,precipitation_ceramic_synthesis,A certain amount of carbon (nominal content of 25  ... ation method without the carbon impregnation step.
5487,10.1016/j.jcat.2013.05.036,precipitation_ceramic_synthesis,"MgAl2O4 support has been prepared by means of a co ... 6 h at 120 degC, and calcined for 7 h at 850 degC."
5488,10.1016/j.apcatb.2006.02.028,precipitation_ceramic_synthesis,Mg/Fe mixed oxide with an Mg/Fe atomic ratio of 0. ... t and finally calcined at 450 degC for 8 h in air.
5489,10.1016/j.matchemphys.2008.06.060,precipitation_ceramic_synthesis,"The layered double hydroxides were prepared by co- ... lled water, and dried at 60 degC in a vacuum oven."
5490,10.1007/s10854-015-3685-9,precipitation_ceramic_synthesis,"In a typical synthesis process, PbWO4 nanocrystals ... O4 powders were then calcined at 550 degC for 3 h."
5491,10.1016/j.mseb.2005.10.002,precipitation_ceramic_synthesis,The samples were prepared by the co-precipitation  ...  air at 800 degC in a rate of 10 degC/min for 1 h.
5492,10.1016/j.cej.2015.11.076,precipitation_ceramic_synthesis,MnFe2O4 was synthesized using co-precipitation met ... d MnFe2O4 sample was calcined at 600 degC for 6 h.
5493,10.1016/j.materresbull.2008.06.021,precipitation_ceramic_synthesis,The ultra-fine NiCuZn-ferrite powders of nominal c ... ere for 1 h to eliminate H2O and any -OH remnants.
5494,10.1016/j.apcatb.2014.06.011,precipitation_ceramic_synthesis,"The Mn0.75Co2.25O4 catalyst was prepared by a co-p ... vernight, and calcined in air at 350 degC for 5 h."
5495,10.1016/j.jcat.2007.06.022,precipitation_ceramic_synthesis,"In the regular coprecipitation route, the two solu ... tion of the resulting LDHs is provided in Table 1."
5496,10.1016/j.apcatb.2016.05.079,precipitation_ceramic_synthesis,ZrO2-CeO2 binary oxide supports were synthesized u ... and ZrO2 (Zr) were prepared with the same process.
5497,10.1016/j.apcata.2008.05.027,precipitation_ceramic_synthesis,"CuO-CeO2 catalyst precursors were prepared with a  ... cedure is described elsewhere [14], [15] and [16]."
5498,10.1016/j.electacta.2011.12.010,precipitation_ceramic_synthesis,"Composites Li1+xMn0.5+0.5xNi0.5-0.5xO2 (x = 0.1, 0 ...  LiOH*H2O was set at 3 wt% excess for all samples."
5499,10.1016/j.matlet.2004.07.065,precipitation_ceramic_synthesis,"10ScSZ powders doped with CeO2 were synthesized by ... Pa, ScSZ ceramic discs were sintered at 1600 degC."
5500,10.1016/j.apsusc.2015.10.212,precipitation_ceramic_synthesis,The N-rGO-ZnO hybrid material was prepared by copr ... er heating at 400 degC for 4 h in tubular furnace.
5501,10.1016/j.cattod.2007.06.021,precipitation_ceramic_synthesis,"The first and second Co3O4-CeO2 catalysts were syn ... nt) and CC-CP2 (KOH as precipitant), respectively."
5502,10.1016/j.cej.2011.06.041,precipitation_ceramic_synthesis,The chemical co-precipitation method was used to s ... f 5 K min-1 for 8 h to obtain single spinel phase.
5503,10.1016/j.fuproc.2015.07.024,precipitation_ceramic_synthesis,The different hexaaluminates were prepared by a co ... 19 and the Ni-2 catalyst is a Ba1Ni0.88Al11.12O19.
5504,10.1016/j.jpcs.2003.08.031,precipitation_ceramic_synthesis,"The Zn2Al-LDHs containing organic UV absorbing ani ... for several times, and dried at 100 degC for 18 h."
5505,10.1016/j.cej.2013.07.020,precipitation_ceramic_synthesis,"Unless otherwise specified, all the reagents used  ... t 400 degC for 6 h to yield yellow color compound."
5506,10.1002/anie.201106702,precipitation_ceramic_synthesis,"The catalysts were prepared by a co-precipitation  ...  (denoted as Ir/Fe-C2 and Ir/Fe-C4, respectively)."
5507,10.1016/j.micromeso.2008.02.032,precipitation_ceramic_synthesis,FeLDH: Iron containing layered double hydroxide wa ... at 723 K for 7 h with a heating rate of 8 K min-1.
5508,10.1016/j.apcata.2004.08.013,precipitation_ceramic_synthesis,Precipitation was carried out for CuO/CeO2 as an e ... was reduced by NaBH4 in the co-precipitation step.
5509,10.1016/j.jcis.2004.11.049,precipitation_ceramic_synthesis,"The Cu0.15Ce0.85O2-y mixed oxide sample was synthe ... ole fractions of copper and cerium, respectively)."
5510,10.1016/j.jallcom.2008.01.152,precipitation_ceramic_synthesis,The strontium ferrite particles were prepared by c ... t was heated for 2 h in air condition at 800 degC.
5511,10.1016/j.cattod.2004.06.040,precipitation_ceramic_synthesis,"For comparison, a CuO/CeO2 catalyst was prepared b ... This procedure gave the catalyst as CuO/CeO2 (CP)."
5512,10.1016/j.matlet.2015.03.133,precipitation_ceramic_synthesis,"The Mn-Fe precursor was synthesized by a chemical  ... Finally, LiMn1/3Fe2/3PO4/C composite was obtained."
5513,10.1016/j.apsusc.2013.04.086,precipitation_ceramic_synthesis,The Cu-Fe-NO3-LDH with the experimental Cu2+/Fe3+  ... th deionized water and dried at 343 K in a vacuum.
5514,10.1016/j.materresbull.2006.04.020,precipitation_ceramic_synthesis,Bimetallic oxide precursors were prepared by the c ... A powder precursor was obtained after calcination.
5515,10.1016/j.mseb.2007.04.004,precipitation_ceramic_synthesis,Pd/α-Fe2O3 powders were prepared by a coprecipitat ... nd 3.0 wt% Pd-doped α-Fe2O3 powders were obtained.
5516,10.1016/j.apcatb.2008.04.024,precipitation_ceramic_synthesis,The CuO-CeO2 mixed oxide was prepared by co-precip ... as calcined at 700 degC under flowing air for 4 h.
5517,10.1016/j.cej.2016.02.020,precipitation_ceramic_synthesis,The MgFe2O4 samples were synthesized by chemical c ... M1 and M2 individually (NaOH: M1 and NH3*H2O: M2).
5518,10.1016/j.jssc.2003.10.010,precipitation_ceramic_synthesis,"The molybdenum-containing vanadium antimonates wer ... orrespond to the pure vanadium antimonate, to Mo4."
5519,10.1016/j.cej.2015.03.009,precipitation_ceramic_synthesis,The Mg3Al-CO3 HTs were prepared by co-precipitatio ... tes (HTs) in a muffle furnace at 450 degC for 2 h.
5520,10.1016/j.apsusc.2017.04.018,precipitation_ceramic_synthesis,A series of Fe-Ce mixed oxides were synthesized by ... nt temperatures in ambient air were also prepared.
5521,10.1016/j.jssc.2006.03.029,precipitation_ceramic_synthesis,Conventional synthesis of LDH by coprecipitation w ...  in a desiccator at room temperature under vacuum.
5522,10.1016/j.jcat.2011.05.026,precipitation_ceramic_synthesis,Mg-Al HT (molar ratio 2:1) was prepared by the sta ...  meixnerite was confirmed by 27Al-MAS-NMR and DRX.
5523,10.1016/j.mseb.2004.04.009,precipitation_ceramic_synthesis,Nanocrystalline NiCuZn ferrite particles were synt ... pe and sintered between 800 and 1000 degC for 2 h.
5524,10.1016/j.cej.2012.01.112,precipitation_ceramic_synthesis,"Methyl orange (C14H14N3NaO3S, abbreviated as MO) a ... gNiAl-CO3 in a muffle furnace at 500 degC for 4 h."
5525,10.1016/j.solidstatesciences.2012.10.008,precipitation_ceramic_synthesis,The sebacate pillared LDH was prepared by a co-pre ... bacate pillared Zn-Al-NO3 LDH (SC-LDH) sol sample.
5526,10.1016/j.matchemphys.2013.03.015,precipitation_ceramic_synthesis,Different Mg-Al-CO3 LDH samples were synthesized b ... water for three times and dried in air at 60 degC.
5527,10.1016/j.apcatb.2010.11.001,precipitation_ceramic_synthesis,Various spinel-type CuxMg1-xAl2O4 (0 <= x < 1) cat ... xMg1-xAl2O4 where x was the ratio of Cu/(Mg + Cu).
5528,10.1016/j.cej.2010.08.083,precipitation_ceramic_synthesis,"The cerium-copper oxide (CeCu, 10 wt.% CuO) was pr ...  60 degC and finally calcined at 300 degC for 2 h."
5529,10.1016/j.jcat.2015.11.020,precipitation_ceramic_synthesis,Mg-Al HTs (molar ratio 2:1) were prepared by the c ... decarbonated water and sonication for 30 min [10].
5530,10.1016/j.fuel.2014.10.004,precipitation_ceramic_synthesis,The sorbents were prepared using a co-precipitatio ... l of the samples were ground to a 40-60 mesh size.
5531,10.1016/j.apcatb.2006.01.021,precipitation_ceramic_synthesis,"Mg-Al hydrotalcite (molar Mg/Al ratio = 3) was pre ... , yielding the as-synthesized hydrotalcite (HTAS)."
5532,10.1016/j.jcat.2013.01.001,precipitation_ceramic_synthesis,"CeO2 was synthesized by the urea gelation/coprecip ... for 12 h, and calcined in air at 400 degC for 4 h."
5533,10.1016/j.electacta.2013.08.156,precipitation_ceramic_synthesis,La2O3-doped ZnO was prepared via a simple calcinat ... e powder. The weight ratio of La2O3 to ZnO is 10%.
5534,10.1016/j.ijhydene.2010.08.091,precipitation_ceramic_synthesis,MgAl2O4 support was prepared by using co-precipita ...  Ni/MgAl2O4 (MgO content was theoretically 25.5%).
5535,10.1016/j.polymdegradstab.2013.01.007,precipitation_ceramic_synthesis,"Pure metal oxides were synthesised by a simple pre ... 00 degC for 8 h, and calcined at 600 degC for 4 h."
5536,10.1016/j.fuproc.2014.05.021,precipitation_ceramic_synthesis,The Al-Ca hydrotalcite support was prepared with A ... esiccator for future use (expressed as Al-Ca-550).
5537,10.1016/j.renene.2015.03.051,precipitation_ceramic_synthesis,The mixed oxide of zirconium and titanium (Zr(OH)4 ...  24 h to obtain a white powder of Zr(OH)4-Ti(OH)4.
5538,10.1016/j.jallcom.2010.04.058,precipitation_ceramic_synthesis,"The nanoparticles of Zn1-XMXS (M = Ni or Cu, X = 0 ... toclave at the temperature of 100 degC within 2 h."
5539,10.1016/j.solidstatesciences.2008.08.003,precipitation_ceramic_synthesis,"Molybdate pillared hydrotalcite (HT-MoO42-) was pr ... ith distilled water, and dried at 75 degC for 8 h."
5540,10.1016/j.cej.2014.07.007,precipitation_ceramic_synthesis,All catalysts were prepared by co-precipitation me ...  mixed solution used for the catalyst preparation.
5541,10.1016/j.micromeso.2004.04.004,precipitation_ceramic_synthesis,The LDH precursors with varying Mg:Al:Ti atomic ra ... g rate of 5 degC/min and used for further studies.
5542,10.1016/j.jnoncrysol.2010.10.019,precipitation_ceramic_synthesis,The undoped and La doped SnO2 powders were synthes ... e grinded and calcined in air at 400 degC for 1 h.
5543,10.1111/j.1744-7402.2008.02351.x,precipitation_ceramic_synthesis,The raw materials used were commercially available ... eratures for 4 h with a heating rate of 300degC/h.
5544,10.1016/j.apcata.2006.02.024,precipitation_ceramic_synthesis,"The Ni-Mg-Al catalysts were prepared by a continuo ... t different temperatures (400, 600, and 800 degC)."
5545,10.1016/j.spmi.2014.10.011,precipitation_ceramic_synthesis,"Fe3O4 NPs were synthesized by a sample chemical co ... dual salts, and finally dried at 60 degC for 24 h."
5546,10.1016/j.elecom.2015.11.004,precipitation_ceramic_synthesis,Thin LDH nanosheets were synthesized in two steps  ... 5 min and dried at 80 degC under vacuum condition.
5547,10.1016/j.apcatb.2015.05.042,precipitation_ceramic_synthesis,"A hydrotalcite-like compound containing Ni, Mg and ... 66/25 and the amount of Ni corresponded to 12 wt%."
5548,10.1016/j.molcata.2006.06.022,precipitation_ceramic_synthesis,Bismuth molybdate catalysts were prepared by a co- ... C for 5 h to yield the bismuth molybdate catalyst.
5549,10.1016/j.jssc.2013.04.007,precipitation_ceramic_synthesis,The pristine Mg3Al-NO3 LDHs were synthesized by th ... was [Mg0.74Al0.26(OH)2](NO3)0.20(CO3)0.03*0.54H2O.
5550,10.1016/j.jcat.2014.08.011,precipitation_ceramic_synthesis,"The Ir/Fe(OH)x catalyst was prepared by a co-preci ... re denoted as Ir/Fe-C2 and Ir/Fe-C4, respectively."
5551,10.1016/j.apcata.2009.12.008,precipitation_ceramic_synthesis,The synthesis of HAP [Ca10(PO4)6(OH)2] was carried ... calcined in air at 900 degC for 30 min before use.
5552,10.1016/j.apcata.2009.04.048,precipitation_ceramic_synthesis,"The catalysts were prepared by co-precipitation of ...  at 350 degC for 30 min, then at 500 degC for 1 h."
5553,10.1016/j.apenergy.2017.02.059,precipitation_ceramic_synthesis,The co-precipitation method involved dissolving Cu ... powder and sieved to a particle size below 125 μm.
5554,10.1016/j.jmmm.2009.10.027,precipitation_ceramic_synthesis,"Ferrite nanoparticles Li0.1(Ni1-xZnx)Fe2.1O4 (x=0, ... ft inside to be slowly cooled to room temperature."
5555,10.1016/j.apsusc.2012.10.131,precipitation_ceramic_synthesis,"Magnetic nanoparticles were prepared by chemical c ...  water, and was diluted to be solid content of 2%."
5556,10.1016/j.cej.2010.03.080,precipitation_ceramic_synthesis,CoFe2O4 magnetic particles were synthesized via co ... yield of 2.5 g of magnetic particles was obtained.
5557,10.1016/j.solidstatesciences.2013.01.009,precipitation_ceramic_synthesis,"For comparison purposes, we also prepared monoclin ... 3 h. We denoted the obtained sample as BiVO4-bulk."
5558,10.1016/j.renene.2013.07.008,precipitation_ceramic_synthesis,Ce(1-x)Zr(x)O2 catalysts were prepared by a co-pre ... (x)O2 catalysts were calcined at 500 degC for 6 h.
5559,10.1016/j.ijhydene.2014.06.103,precipitation_ceramic_synthesis,The Gd0.1Ce0.9O1.95 (GDC) powders were prepared by ... pitates were calcined at 700 and 900 degC for 2 h.
5560,10.1016/j.cej.2011.02.075,precipitation_ceramic_synthesis,LDH containing carbonate as the interlayer anion w ... g the LDH in a muffle furnace at 450 degC for 4 h.
5561,10.1016/j.ijhydene.2012.08.055,precipitation_ceramic_synthesis,A series of CexZr1-xO2-based Cu catalysts was prep ... calcined at 600 degC for 4 h at 5 degC/min in air.
5562,10.1016/j.matchemphys.2016.07.047,precipitation_ceramic_synthesis,"All chemical reagents were analytical grade and us ... ed water for 6 min, and dried at 70 degC for 12 h."
5563,10.1016/j.apcatb.2016.03.014,precipitation_ceramic_synthesis,The Cu/ZnO/ZrO2 catalysts with the mole ratio of C ...  denoted as CZZ-x (x is the NaBH4/Cu molar ratio).
5564,10.1016/j.electacta.2008.03.066,precipitation_ceramic_synthesis,"As a contrast to the two-step drying method, Ni1/3 ... d dried at 120 degC for 2 h in vacuum drying oven."
5565,10.1016/j.molcata.2010.03.018,precipitation_ceramic_synthesis,CaO-ZrO2 solid solution was prepared by co-precipi ... the same as those reported in the literature [42].
5566,10.1016/j.jeurceramsoc.2005.06.021,precipitation_ceramic_synthesis,The CS4/LDHs was prepared by the coprecipitation m ... ater and dried at 40 degC for 24 h in vacuum oven.
5567,10.1016/j.ssi.2004.04.027,precipitation_ceramic_synthesis,The HT phase with the composition of Mg0.74Al0.26( ...  (200-600 degC) for 5 h prior to characterization.
5568,10.1016/j.electacta.2011.11.109,precipitation_ceramic_synthesis,ITO nanoparticles were synthesized by a coprecipit ... er was obtained after grinding in an agate mortar.
5569,10.1016/j.elecom.2008.08.023,precipitation_ceramic_synthesis,The Ce0.8Sm0.2O1.9 (SDC) was synthesized by carbon ... a2CO3 composite with Na2CO3 weight content of 20%.
5570,10.1016/j.cattod.2016.02.061,precipitation_ceramic_synthesis,CeSiOx catalyst support was synthesized by co-prec ... urnace. The nominal CeO2:SiO2 weight ratio is 8.6.
5571,10.1016/j.susc.2015.11.010,precipitation_ceramic_synthesis,A catalyst was also prepared using a conventional  ... he final iron molybdate catalyst with Fe:Mo 1:2.2.
5572,10.1016/j.apcatb.2007.01.008,precipitation_ceramic_synthesis,The catalysts were synthesized by the coprecipitat ... nMx where M was Fe or Ni and x was the aging time.
5573,10.1007/s10008-014-2651-4,precipitation_ceramic_synthesis,"The modification of Lu(OH)3 on a layered double hy ... 8, which is employed as a reference in this study."
5574,10.1016/j.actamat.2005.10.004,precipitation_ceramic_synthesis,The synthesis of Ce0.8Sm0.2O1.9 (SDC) by the carbo ... d calcined at 600 degC in air for 2 h to form SDC.
5575,10.1016/j.cattod.2015.06.029,precipitation_ceramic_synthesis,BiMoCex catalysts (x = 0-0.4) were prepared by con ... re x is the molar ratio of cerium in the catalyst.
5576,10.1016/j.jpowsour.2014.10.196,precipitation_ceramic_synthesis,"Materials synthesis: FeNiHCF was precipitated by a ... ed water, and dried in vacuum at 90 degC for 20 h."
5577,10.1016/j.jpowsour.2014.11.080,precipitation_ceramic_synthesis,"Fe0.6Mn0.4C2O4*2H2O was prepared by co-precipitati ... es, then dried in vacuum oven at 70 degC for 12 h."
5578,10.1016/j.apcatb.2007.12.007,precipitation_ceramic_synthesis,MnOx-CeO2 mixed oxides with Mn/(Mn + Ce) molar rat ... 3 K for 12 h and calcined at 773 K for 6 h in air.
5579,10.1016/j.matlet.2010.07.011,precipitation_ceramic_synthesis,All chemicals used were of analytical grade and pu ... inally dried in a vacuum oven at 60 degC for 12 h.
5580,10.1016/j.apcatb.2010.09.026,precipitation_ceramic_synthesis,"CZ and La modified CZ (CZL) supports were prepared ... es are referred to as CZa and CZLxa, respectively."
5581,10.1016/j.apcata.2005.06.007,precipitation_ceramic_synthesis,"To prepare synthetic hydrotalcite, we first dissol ... t 500 degC for 16 h to produce MgAlOx mixed oxide."
5582,10.1016/j.apcatb.2010.10.008,precipitation_ceramic_synthesis,"A range of Au/CuMnOx catalysts were prepared by a  ... d at 300, 400 and 500 degC in static air for 16 h."
5583,10.1016/j.cej.2008.01.016,precipitation_ceramic_synthesis,"The MnOx-CeO2 mixed oxide (Mn/(Mn + Ce) = 0.5, mol ... 3 K for 12 h and calcined at 773 K for 6 h in air."
5584,10.1016/j.carbon.2009.09.062,precipitation_ceramic_synthesis,Monodisperse CoFe2O4 magnetic nanoparticles with d ... es were dried in a vacuum oven at 50 degC for 3 h.
5585,10.1016/j.chemosphere.2007.05.009,precipitation_ceramic_synthesis,All reagents were purchased from Kanto Chemical (T ... d with the chemical composition Mg0.80Al0.20O1.10.
5586,10.1016/j.electacta.2014.10.093,precipitation_ceramic_synthesis,The layered oxide LiNi0.8Co0.1Mn0.1O2 powders were ...  heated at 750 degC for 15 h under flowing oxygen.
5587,10.1016/j.cattod.2007.06.038,precipitation_ceramic_synthesis,Ni/ZnO samples were synthesized by co-precipitatio ... and passivated in the same way as Ni/SiO2 samples.
5588,10.1016/j.apcata.2003.09.028,precipitation_ceramic_synthesis,The gold catalysts were prepared by co-precipitati ... t the corresponding temperature continued for 2 h.
5589,10.1016/j.susc.2015.12.011,precipitation_ceramic_synthesis,"NiFe2O4 catalyst was synthesized with a co-precipi ... 4 h, by which NiFe2O4 nanoparticles were prepared."
5590,10.1016/j.matlet.2014.08.065,precipitation_ceramic_synthesis,"Nd2-xZr2+xO7+x/2 (x=0, 0.1, 0.2, 0.3, 0.4, 0.5) po ...  materials for mechanical properties measurements."
5591,10.1016/j.apcatb.2012.08.020,precipitation_ceramic_synthesis,CeO2-Al2O3 catalysts were prepared by a co-precipi ...  Al2O3 and CeO2 were prepared in a similar manner.
5592,10.1016/j.apcata.2009.04.004,precipitation_ceramic_synthesis,"The Co-Mn-Al LDH precursor was prepared by copreci ... as 0K, i.e., parent (non-modified) Co4MnAl sample."
5593,10.1016/j.elecom.2010.12.019,precipitation_ceramic_synthesis,The Ce0.9Gd0.1O2-δ (GDC) was synthesized by carbon ... nal composition in weight ratio of 40LiNiO2-60GDC.
5594,10.1016/j.jcat.2004.12.007,precipitation_ceramic_synthesis,The CuO-ZnO-Al2O3 precursor (Cu:Zn:Al = 60:30:10 a ... ned at 350 degC in flowing air for 6 h (catalyst).
5595,10.1016/j.matlet.2011.02.034,precipitation_ceramic_synthesis,The Y3 - XGdXFe5O12system was prepared by a revers ... C to 1200 degC for 1 h in ambient air [5] and [8].
5596,10.1016/j.matchemphys.2012.02.007,precipitation_ceramic_synthesis,Fig. 1 shows the block diagram of coprecipitation  ... are reported in our previous articles [7] and [8].
5597,10.1016/j.matlet.2005.12.129,precipitation_ceramic_synthesis,Powders of nanocrystalline ZrO2-Y2O3-Al2O3 were sy ... posite oxides in the subsequent characterizations.
5598,10.1016/j.jcat.2010.07.014,precipitation_ceramic_synthesis,The Pd/Fe3O4 catalyst was prepared by the co-preci ... . The as-reduced catalyst was denoted as Pd/Fe3O4.
5599,10.1016/j.apcatb.2015.04.042,precipitation_ceramic_synthesis,"The SnO2, CeO2 and Sn1-xCexO2 (x=0.1, 0.3, 0.5, 0. ... eoretical molar proportion of Ce to substitute Sn."
5600,10.1016/j.ijhydene.2015.06.170,precipitation_ceramic_synthesis,The conventional coprecipitation method was employ ... ir atmosphere with the heating rate of 5 degC/min.
5601,10.1016/j.jallcom.2014.02.034,precipitation_ceramic_synthesis,"For comparison, the synthesis of (Ni0.25Mn0.75)CO3 ... 1.5O4 were similar to the ones as mentioned above."
5602,10.1016/j.fuproc.2008.03.006,precipitation_ceramic_synthesis,"CeO0.75Zr0.25O2 and doped CeO0.75Zr0.25O2 were pre ... erence, CeO2 was also prepared by the same method."
5603,10.1016/j.apsusc.2017.04.137,precipitation_ceramic_synthesis,The bifunctional Fe-Zr composites were synthesized ... terial was stored in a desiccator for further use.
5604,10.1007/s10854-011-0351-8,precipitation_ceramic_synthesis,Nano particles of Co(0.5-x)NixZn0.5Fe2O4 with x-va ... ions and the results are published elsewhere [14].
5605,10.1007/s10853-017-0826-y,precipitation_ceramic_synthesis,Mg-Al-NO3 was prepared by a coprecipitation method ... dried at 90 degC for 24 h to obtain Mg-Al-NO3 LDH.
5606,10.1016/j.cattod.2007.10.059,precipitation_ceramic_synthesis,"For the preparation of doped precursors, the well  ... air at 385 K overnight and denoted as Precursor B."
5607,10.1016/j.electacta.2013.02.037,precipitation_ceramic_synthesis,"LiOH*H2O, Ni(NO3)2*6H2O, Mn(NO3)2*6H2O and Co(NO3) ... nt of NH4F and heating at 450 degC for 5 h in air."
5608,10.1016/j.jmmm.2015.05.082,precipitation_ceramic_synthesis,"In this study, the compounds of composition of Y3A ... paration process is schematically shown in Fig. 1."
5609,10.1016/j.cej.2015.10.004,precipitation_ceramic_synthesis,The co-precipitation method was adopted for the pr ... ed water and dried in an oven at 80 degC for 12 h.
5610,10.1016/j.cattod.2006.05.015,precipitation_ceramic_synthesis,The CeO2-ZrO2-Bi2O3 solid solutions were prepared  ... lso prepared by the same procedure for comparison.
5611,10.1016/j.apcata.2005.12.003,precipitation_ceramic_synthesis,Natural phosphate used in this work comes from an  ... 0 degC and calcined in air at 900 degC for 30 min.
5612,10.1016/j.cattod.2011.05.014,precipitation_ceramic_synthesis,Ce0.65Zr0.30La0.05O2 solid solution was prepared b ... h. The nominal content of La2O3 was about 4.6 wt%.
5613,10.1016/j.cattod.2011.09.042,precipitation_ceramic_synthesis,The CuxCryOz mixed oxide was prepared by the stand ... e material obtained was calcined at 873 K for 3 h.
5614,10.1016/j.ssi.2007.06.010,precipitation_ceramic_synthesis,The procedures for preparation of layered LiNi0.5M ...  900 degC for 24 h in air after thorough grinding.
5615,10.1016/j.cattod.2011.04.043,precipitation_ceramic_synthesis,CZ doped by nickel oxide with different content wa ...  1000 degC for 4 h in air to obtain aged supports.
5616,10.1016/j.actamat.2013.11.028,precipitation_ceramic_synthesis,Anhydrous Ag2C2O4 and NiC2O4 crystals were synthes ... tion between 0.4 and 0.6 produced similar results.
5617,10.1016/j.electacta.2012.05.145,precipitation_ceramic_synthesis,"Reagents were all of AR grade. Water used in the s ... several times, and then dried at 60 degC for 12 h."
5618,10.1016/j.cej.2015.10.055,precipitation_ceramic_synthesis,The CeTi nanoparticles were prepared by co-precipi ... 20 degC for 24 h and calcined at 500 degC for 4 h.
5619,10.1016/j.apcatb.2013.12.019,precipitation_ceramic_synthesis,The layered double hydroxide support containing Zn ... ith distilled water and dried at room temperature.
5620,10.1016/j.jssc.2006.01.012,precipitation_ceramic_synthesis,The CS/LDHs were prepared by the coprecipitation m ... er and dried in a vacuum oven at 40 degC for 24 h.
5621,10.1002/cplu.201500054,precipitation_ceramic_synthesis,Three different nanostructures of MnO2 such as nan ... prepared without and the other two with templates.
5622,10.1016/j.jpowsour.2006.02.045,precipitation_ceramic_synthesis,MnO2*xH2O was prepared by chemical co-precipitatio ... n MnO2*xH2O/CRF composite materials were obtained.
5623,10.1016/j.jpowsour.2011.05.013,precipitation_ceramic_synthesis,Synthesis of non-spherical Ni(OH)2 powders was car ... (at 120 degC for 2 h) to obtain the final product.
5624,10.1016/j.optmat.2004.10.001,precipitation_ceramic_synthesis,"Preparation of YPO4 by co-precipitation method: Y2 ... ount of flux, and then fired at 1000 degC for 2 h."
5625,10.1007/s11144-009-0120-3,precipitation_ceramic_synthesis,To an iron free sulfuric acid digested aqueous sol ... stilled water and then dried overnight at 90 degC.
5626,10.1016/j.snb.2014.01.086,precipitation_ceramic_synthesis,The ZnWO4 powders were prepared by means of coprec ... ded thoroughly to achieve the final ZnWO4 powders.
5627,10.1007/s10853-012-7076-9,precipitation_ceramic_synthesis,Al2Mo3O12 nanopowder was prepared through co-preci ... 0 degC and maintained at this temperature for 5 h.
5628,10.1016/j.cattod.2013.10.042,precipitation_ceramic_synthesis,"The Cu/ZnO catalyst (Cu/Zn = 1:1, molar ratio) was ... nd then screened into the size between 20-40 mesh."
5629,10.1016/j.jallcom.2015.05.097,precipitation_ceramic_synthesis,The precursor (FePO4[?]2H2O) for LiFePO4/C was pre ... 0 degC in air for 4 h to obtain crystalline FePO4.
5630,10.1002/ceat.201400668,precipitation_ceramic_synthesis,Promoted Fe-Al-Cu catalysts with Fe/Al = 10 and Fe ... nd calcined at 400 degC for 4 h in air atmosphere.
5631,10.1016/j.cej.2007.03.057,precipitation_ceramic_synthesis,The CeO2-ZrO2 mixed oxide support was prepared by  ... ed to a size 50-70 mesh before metal impregnation.
5632,10.1007/s10853-014-8321-1,precipitation_ceramic_synthesis,"In the co-precipitation method, freshly prepared a ... s have been characterized from various techniques."
5633,10.1016/j.cej.2013.03.118,precipitation_ceramic_synthesis,"All chemicals were of the highest quality commerci ... 3, and Fe(NO3)3 solutions was prepared in advance."
5634,10.1016/j.cej.2012.01.003,precipitation_ceramic_synthesis,"MoZnAlO catalysts with different Zn/Al molar ratio ... ure, the resulting solid was the MoZnAlO catalyst."
5635,10.1016/j.apcatb.2009.09.036,precipitation_ceramic_synthesis,The mixed oxide supports were prepared by coprecip ... ed oxide with 75 wt.% of CeO2 and 25 wt.% of ZrO2.
5636,10.1016/j.jallcom.2011.08.058,precipitation_ceramic_synthesis,The co-precipitation method was applied for the pr ... icles were precalcined in air at 400 degC for 2 h.
5637,10.1016/j.apsusc.2005.11.062,precipitation_ceramic_synthesis,Ce0.6Zr0.4O2 was prepared by a co-precipitation te ... ). This material is hereafter referred to as CZ60.
5638,10.1016/j.biocel.2015.12.002,precipitation_ceramic_synthesis,"Bare SPIONs were synthesized by the alkaline copre ... 6,500 x G; 45 min) to remove aggregates (Eq. (1))."
5639,10.1007/s10854-016-5927-x,precipitation_ceramic_synthesis,CoFe2O4-coated poly(acrylonitrile) microspheres we ... d on the calculation of weight gain after plating.
5640,10.1016/j.ssi.2013.09.009,precipitation_ceramic_synthesis,"Ni-Fe LDH intercalated with CO32 - (Ni-Fe CO32 - L ... washed with distilled water, and dried at 80 degC."
5641,10.1016/j.jcat.2011.01.016,precipitation_ceramic_synthesis,Supported [Bmim]3PMo12O40 was prepared by a co-pre ... asured on a Micromeritics Tristar 3020 instrument.
5642,10.1016/j.cemconres.2004.05.012,precipitation_ceramic_synthesis,The CaAl LDH was prepared by a pH-controlled copre ... ial was then dried for 16 h at 100 degC in vacuum.
5643,10.1016/j.electacta.2013.11.124,precipitation_ceramic_synthesis,The transition metal (TM) hydroxides precursor (Ni ... d dried in an oven at 100 degC for 10 h in vacuum.
5644,10.1016/j.jcat.2016.02.025,precipitation_ceramic_synthesis,The CuO-ZnO-Al2O3 precursor (Cu:Zn:Al = 60:30:10 a ... h yielding the oxide CuO-ZnO-Al2O3 (CZA) catalyst.
5645,10.1016/j.jallcom.2015.12.076,precipitation_ceramic_synthesis,The flaky graphite/cobalt zinc ferrite composites  ... s were obtained after cooling to room temperature.
5646,10.1016/j.matchemphys.2014.06.071,precipitation_ceramic_synthesis,Heterostructured TiO2/BiOCl nanocomposite photocat ... ation method and heat treated at 400 degC for 2 h.
5647,10.1016/j.cattod.2014.07.035,precipitation_ceramic_synthesis,The CeMoOx catalyst samples were prepared with a u ... denoting the calcination temperature after CeMoOx.
5648,10.1016/j.jcat.2010.03.015,precipitation_ceramic_synthesis,"V2O5-Al2O3 supports with vanadia contents of 0, 10 ... adia content in weight percentage in the Vx-Al2O3."
5649,10.1016/j.jcat.2007.09.015,precipitation_ceramic_synthesis,The Mg-Al hydrotalcite (Mg/Al molar ratio = 4) was ...  were kept under inert atmosphere for further use.
5650,10.1016/j.jhazmat.2009.12.116,precipitation_ceramic_synthesis,"For coprecipitation method, manganese nitrate (0.0 ... , the samples were calcinated at 500 degC for 6 h."
5651,10.1016/j.cattod.2016.06.005,precipitation_ceramic_synthesis,The preparative methods adopted in this study were ... ere calcined in open air at 450 degC for 9 h [22].
5652,10.1016/j.snb.2008.01.064,precipitation_ceramic_synthesis,The Co-Ce oxides were prepared by the co-precipita ... peratures ranged from 250 degC to 500 degC in air.
5653,10.1016/j.cej.2011.06.053,precipitation_ceramic_synthesis,The SnO2/ZnO QDs heterojunction were prepared by a ... degC in air to obtain SnO2/ZnO QDs heterojunction.
5654,10.1016/j.electacta.2015.10.031,precipitation_ceramic_synthesis,A simple co-precipitation method was used to synth ... 35 degC for 72 h and then at 170 degC for 3 hours.
5655,10.1016/j.cattod.2012.07.029,precipitation_ceramic_synthesis,The catalysts were synthesized by citrate and copr ... ontains 30 wt.% Cu and is labeled Cu(30)/ZnO(COP).
5656,10.1016/j.apcatb.2012.07.008,precipitation_ceramic_synthesis,CeO2 and Ru-CeO2 catalysts were prepared by precip ... henium is 0.02 g mL-1) to Ce(NH4)2(NO3)6 solution.
5657,10.1016/j.jcis.2013.02.004,precipitation_ceramic_synthesis,The adsorbent of mesoporous Ce-Fe binary oxides (M ... the effect of calcination on the property of MCFO.
5658,10.1002/ejic.201402602,precipitation_ceramic_synthesis,4.2.1. Direct Synthesis of Oleic Acid/LDH: The hyb ... ion and dried at 30 degC for 24 h before grinding.
5659,10.1016/j.cattod.2010.11.032,precipitation_ceramic_synthesis,Mg-Al layered double hydroxides (LDH) with Mg/Al r ...  flow at 723 K for 7 h to obtain the mixed oxides.
5660,10.1016/j.cattod.2011.06.006,precipitation_ceramic_synthesis,ZnO-supported cobalt catalysts and the catalyst su ... port in all catalysts contained 5 wt.% of alumina.
5661,10.1016/j.cattod.2014.06.035,precipitation_ceramic_synthesis,Mg-Al hydrotalcites were prepared using an adapted ... efore being sieved to a 212-425 μm sieve fraction.
5662,10.1007/s10854-011-0565-9,precipitation_ceramic_synthesis,"Nanoparticles of MnBixFe2-xO4 (with x = 0.0, 0.02, ... ples are then sintered in air for 5 h at 500 degC."
5663,10.1016/j.cej.2011.03.019,precipitation_ceramic_synthesis,"Mg-Fe-CO3 (LDH), with various Mg/Fe molar ratios o ... ng 8 h. The obtained solid was designated as CLDH."
5664,10.1016/j.apcata.2004.10.025,precipitation_ceramic_synthesis,"The support, TiO2-ZrO2, with a molar ratio of 1:1  ... d support had a N2 BET surface area of 170 m2 g-1."
5665,10.1016/j.jallcom.2014.01.155,precipitation_ceramic_synthesis,Magnetite nanoparticles were obtained by chemical  ... s dried in a vacuum oven at 30 +- 5 degC for 24 h.
5666,10.1016/j.electacta.2016.01.090,precipitation_ceramic_synthesis,The ionic material Sm0.2Ce0.8O1.9 (SDC) was synthe ... degC in air for 4 h to get final SDC product [31].
5667,10.1016/j.cej.2012.08.037,precipitation_ceramic_synthesis,For the preparation of the hydrotalcite precursors ...  air to obtain the NiMgAlLa mixed-oxide catalysts.
5668,10.1016/j.jmatprotec.2007.12.093,precipitation_ceramic_synthesis,Precursor powders were produced via coprecipitatio ... C/min in a Dr. Sinter type SPS3.20 MK-V apparatus.
5669,10.1016/j.cej.2010.12.042,precipitation_ceramic_synthesis,Ce-Zr-O2 (designated as CZ) and Mn doping samples  ... 700 degC for 6 h in air to get the final supports.
5670,10.1016/j.cattod.2007.06.024,precipitation_ceramic_synthesis,Hydrotalcites with different Mg:Al molar ratios (x ... C for 8 h. The final product was mentioned as HTx.
5671,10.1016/j.apcatb.2008.01.007,precipitation_ceramic_synthesis,"MnOx modified Co3O4-CeO2 catalysts were prepared b ... nd c represented the molar ratio of Co, Ce and Mn."
5672,10.1016/j.matlet.2009.10.043,precipitation_ceramic_synthesis,In the second technique (the co-precipitation tech ... ed in air at 150 degC to obtain precursor powders.
5673,10.1016/j.jpcs.2005.09.072,precipitation_ceramic_synthesis,The Mg-Al-LDH with a Mg/Al molar ratio of 2.0 was  ... position was [Mg0.66Al0.34(OH)2](CO3)0.17*0.76H2O.
5674,10.1016/j.apcata.2003.10.025,precipitation_ceramic_synthesis,"Nanometer coupled oxide ZnO-SnO2 was prepared usin ... H2O for SnO2 and ZnSO4*7H2O for ZnO, respectively."
5675,10.1016/j.matchemphys.2009.01.005,precipitation_ceramic_synthesis,The 50/50 CuO/CeO2 and the 25/25/50 CuO/Co3O4/CeO2 ...  110 degC and calcined in air at 600 degC for 3 h.
5676,10.1002/cphc.201200665,precipitation_ceramic_synthesis,Samples were prepared by a co-precipitation method ...  was calculated to give a gold loading of 6 wt. %.
5677,10.1016/j.jcat.2012.06.011,precipitation_ceramic_synthesis,"AgBr-BiOBr samples were synthesized using a co-pre ... tilled water, and then dried at 65 degC overnight."
5678,10.1016/j.cej.2016.07.061,precipitation_ceramic_synthesis,Mixed oxides zirconium-titanium (ZrTiO) were prepa ... respectively with air at 400 and 500 degC for 2 h.
5679,10.1016/j.jssc.2006.11.009,precipitation_ceramic_synthesis,The TiO2-ZrO2 mixed oxide (1:1 molar ratio) suppor ... cipitate was finally calcined at 500 degC for 6 h.
5680,10.1016/j.electacta.2014.10.151,precipitation_ceramic_synthesis,The spherical Ni0.5Mn0.5CO3 carbonate precursor wa ... nside a vacuum oven at 110 degC for several hours.
5681,10.1016/j.cattod.2014.02.050,precipitation_ceramic_synthesis,A hydrotalcite with a Mg/Al ratio of 3 was synthes ... ls on the preparation procedure are given in [31].
5682,10.1007/s10853-016-9733-x,precipitation_ceramic_synthesis,"All the materials are composed of CeO2-ZrO2-La2O3- ... rials signed as CZ-1000 and CZ-1100, respectively."
5683,10.1016/j.ceramint.2011.08.018,precipitation_ceramic_synthesis,In the co-precipitation method the Sr(II) and Fe(I ...  ethanol (volume ratio 1:1) and dried at 100 degC.
5684,10.1016/j.apcata.2004.02.011,precipitation_ceramic_synthesis,"A ZnO-Cr2O3 (Zn:Cr=8:2, mol ratio) support was pre ... 2 h, and calcined in air flow at 500 degC for 1 h."
5685,10.1016/j.cej.2015.08.027,precipitation_ceramic_synthesis,The 30%CuO/ZrO2-CP catalyst was prepared by a co-p ... 383 K and calcined at 673 K in static air for 4 h.
5686,10.1016/j.matchemphys.2012.05.017,precipitation_ceramic_synthesis,Nanoparticle Li[Ni1/3Co1/3Mn1/3]O2 was prepared us ...  for 10 h to take nanosized Li[Ni1/3Co1/3Mn1/3]O2.
5687,10.1016/j.fuproc.2008.08.008,precipitation_ceramic_synthesis,"The catalysts with different Mg/Zr ratios (1:1, 2: ... th weight ratios of 1:1, 2:1 and 3:1 respectively."
5688,10.1016/j.elecom.2009.10.023,precipitation_ceramic_synthesis,The LiFePO4/graphene composites were prepared usin ...  same procedure except that no graphene was added.
5689,10.1016/j.cej.2014.09.059,precipitation_ceramic_synthesis,Pyromellitic acid intercalated ZnAl-LDHs were synt ... or the following experiments and characterization.
5690,10.1016/j.fuel.2008.04.015,precipitation_ceramic_synthesis,Ce0.75Zr0.25O2 solid solution was also prepared by ... in an air flow. The sample was labeled as CZ-CTAB.
5691,10.1002/cssc.200800085,precipitation_ceramic_synthesis,Synthesis of hydrotalcite-based materials: The met ... KxHT* (Kx stands for the amount of K2CO3 in wt %).
5692,10.1007/s10854-016-4409-5,precipitation_ceramic_synthesis,SrMoO4 and Eu3+(Dy3+)-doped SrMoO4 phosphors have  ... ral times. The washed powder was dried at 80 degC.
5693,10.1016/j.electacta.2011.05.071,precipitation_ceramic_synthesis,The LiCoPO4 coated Li1.2Ni0.18Mn0.59Co0.03O2 was p ... d at 500 degC for 3 h to obtain the final product.
5694,10.1016/j.jmmm.2011.02.017,precipitation_ceramic_synthesis,Nanoparticles of Mn0.5Zn(0.5-x)CdxFe2O4 with x var ... ration sample magnetometer (Lakeshore Model 7000).
5695,10.1016/j.cej.2015.04.122,precipitation_ceramic_synthesis,The sorbents were synthesized by coprecipitation o ... were calcined at 200 degC to produce the sorbents.
5696,10.1002/advs.201500199,precipitation_ceramic_synthesis,Synthesis of Electrocatalysts: The materials were  ... m the same procedure except the addition of Tween.
5697,10.1016/j.matchemphys.2012.01.025,precipitation_ceramic_synthesis,Yb3+/Er3+ codoped Gd6WO12 nanoparticles were prepa ... er the precursor was sintered at 900 degC for 1 h.
5698,10.1016/j.apenergy.2014.12.042,precipitation_ceramic_synthesis,A typical precipitated Fe-Mn-K-SiO2 catalyst used  ... as follows Fe:Mn:K:Si = 100:15:3:30 (molar ratio).
5699,10.1016/j.cej.2012.01.068,precipitation_ceramic_synthesis,SO42-/ZnO-TiO2: Zn-Ti hydroxide gel was prepared b ... he following based on the calcination temperature.
5700,10.1016/j.electacta.2013.06.033,precipitation_ceramic_synthesis,Nine (CoxNi1-x)2Al-NO3 LDH compounds (with x = 0;  ... nized water and dried in air at 30 degC overnight.
5701,10.1016/j.jcat.2004.10.006,precipitation_ceramic_synthesis,Mono- and bimetal catalysts were prepared by using ... etermined by atomic absorption spectroscopy (AAS).
5702,10.1016/j.apcatb.2010.11.043,precipitation_ceramic_synthesis,The MnOx-promoted Co3O4 samples (denoted as Mn-Co- ... nO2 samples were prepared with the same procedure.
5703,10.1016/j.apcatb.2006.03.003,precipitation_ceramic_synthesis,CuZnOx was also prepared by a co-precipitation met ... d by calcination in static air (400 degC for 6 h).
5704,10.1016/j.electacta.2014.10.072,precipitation_ceramic_synthesis,"LiCoO2 powder, with an average particle size of 10 ...  900 degC for 20h in air to obtain LiCoO2 powders."
5705,10.1016/j.jcat.2009.09.029,precipitation_ceramic_synthesis,"A constant pH coprecipitation method was used to p ...  denoted as CHT for ""coprecipitated hydrotalcite""."
5706,10.1016/j.nanoen.2015.11.015,precipitation_ceramic_synthesis,SCDC: Synthesis of SCDC was performed through co-p ... sintered at 700 degC in air for 4 h to obtain SDC.
5707,10.1016/j.cherd.2016.09.032,precipitation_ceramic_synthesis,Synthesis of Fe3O4 nanoparticles. Fe3O4 nanopartic ... s with average diameter of 10 nm will be obtained.
5708,10.1016/j.cej.2014.11.138,precipitation_ceramic_synthesis,"The precursor was synthesized via co-precipitation ... 3 (crystalline Sm(OH)3) and Co(OH)2, respectively."
5709,10.1016/j.matchemphys.2010.02.049,precipitation_ceramic_synthesis,"The uniform and highly dispersed super-paramagneti ...  of Fe3O4 and B2O3, and then calcined at 450 degC."
5710,10.1016/j.ssi.2014.06.012,precipitation_ceramic_synthesis,The Li-rich layered Li1.2Mn0.54Ni0.13Co0.13O2 was  ... ain the desired product Li1.2Mn0.54Ni0.13Co0.13O2.
5711,10.1016/j.elecom.2004.11.011,precipitation_ceramic_synthesis,The LDH containing interlayer carbonate was prepar ... der was dried in air at room temperature for 24 h.
5712,10.1016/j.cej.2010.07.064,precipitation_ceramic_synthesis,The 5.0 wt.% CuO-CeO2 catalyst was prepared by a c ... the same method for the supplementary experiments.
5713,10.1016/j.apcatb.2012.07.020,precipitation_ceramic_synthesis,"Briefly, for the synthesis of 1:2 molar ratio of L ... omposite perovskite (hereafter denoted as sc-LCM)."
5714,10.1016/j.jelechem.2014.06.023,precipitation_ceramic_synthesis,Spinel LiMn2O4 particles (size: 0.8 μm) were purch ... ater several times and dried overnight at 60 degC.
5715,10.1016/j.cattod.2009.11.006,precipitation_ceramic_synthesis,Double layered materials containing ZnAlFe at diff ... nditions to that used for the ZnAlFe mixed oxides.
5716,10.1016/j.micromeso.2014.08.049,precipitation_ceramic_synthesis,The ordered mesoporous iron manganese bimetal oxid ...  6 h. The final obtained powder was denoted as IM.
5717,10.1016/j.cej.2015.08.117,precipitation_ceramic_synthesis,"The HTLCs catalysts were synthesized by the co-pre ... , while the mole ratio of M2+/M3+ was from 1 to 5."
5718,10.1016/j.matchemphys.2016.01.056,precipitation_ceramic_synthesis,Magnetic nanoparticles (MNPs) were prepared by co- ...  acetone and dried in an oven at 50 degC for 24 h.
5719,10.1016/j.apcatb.2014.06.048,precipitation_ceramic_synthesis,All the mixed oxides catalysts were prepared by co ... eO2 catalyst was also prepared by the same method.
5720,10.1016/j.matlet.2005.02.003,precipitation_ceramic_synthesis,A coprecipitation method was developed to synthesi ... ined temperature between 700 and 900 degC for 1 h.
5721,10.1016/j.nimb.2005.11.009,precipitation_ceramic_synthesis,"In the second case, synthesis of Mn0.75Zn0.18Fe2.0 ... ntly heat treated at 400 degC for crystallization."
5722,10.1007/s10854-011-0395-9,precipitation_ceramic_synthesis,Nanoparticles of Co0.5Zn0.5BixFe(2-x)O4 with x val ... powder samples are used for magnetization studies.
5723,10.1016/j.apcatb.2011.04.006,precipitation_ceramic_synthesis,"CZ doped by nickel oxide was prepared through a co ... 4 h to obtain support, which was denoted as CZN-s."
5724,10.1016/j.optmat.2016.07.026,precipitation_ceramic_synthesis,All the chemicals used in our experiment were of a ... red amorphous products at 800 degC for 1 h in air.
5725,10.1016/j.cattod.2011.08.016,precipitation_ceramic_synthesis,HT-HM (Mg/Al = 5) catalysts were prepared by conve ...  also prepared by the above method with 3 h aging.
5726,10.1016/j.electacta.2014.10.078,precipitation_ceramic_synthesis,"LiOH*H2O (98%, Aldrich), Ni(NO3)2*6H2O (98%, Fluka ...  final products were quenched to room temperature."
5727,10.1016/j.ijhydene.2011.01.078,precipitation_ceramic_synthesis,"For the coprecipitation of hydroxides, 2.65 g (0.7 ... , a solid solution of ceria-zirconia was obtained."
5728,10.1002/app.25840,precipitation_ceramic_synthesis,DS-LDH was prepared by coprecipitation method. NaO ...  washed and dried at 60degC under vacuum for 72 h.
5729,10.1016/j.cej.2014.11.096,precipitation_ceramic_synthesis,The active component PdCl2 was loaded on the suppo ... nted the mass ration of MO and M denoted Cu or Pb.
5730,10.1016/j.jpowsour.2013.03.143,precipitation_ceramic_synthesis,The bare LiMn1.58Ni0.42O4 sample was synthesized b ... en were dried in an air oven at 100 degC for 24 h.
5731,10.1016/j.cattod.2008.06.026,precipitation_ceramic_synthesis,"Three copper-based mixed oxides, CuO-CeO2, CuO-CeO ... ed in air in a muffle furnace at 500 degC for 4 h."
5732,10.1016/j.apcatb.2012.08.006,precipitation_ceramic_synthesis,The Co/Mg/Al hydrotalcite with formula [Co2Mg4Al2( ... h to obtain the hydrotalcite-derived mixed oxides.
5733,10.1016/j.matlet.2013.04.001,precipitation_ceramic_synthesis,Co-precipitation (CP) method: Carbonate based co-p ... green compacts were sintered at 900 degC for 12 h.
5734,10.1007/s00339-013-7827-8,precipitation_ceramic_synthesis,MnFe2O4 nanoparticles were prepared by a modified  ... d dried at 60 degC under 200 mbar (in air) for 24.
5735,10.1016/j.apenergy.2011.11.083,precipitation_ceramic_synthesis,"The Fe-modified CuMnZnO catalysts were prepared by ... Fe0.30CuMnZnO, and Fe0.45CuMn2.0ZnO, respectively."
5736,10.1016/j.jcat.2008.06.009,precipitation_ceramic_synthesis,Fresh CeO2-ZrO2 mixed oxides (CZf) were obtained b ... e mixed oxides could be denoted as Ce0.67Zr0.33O2.
5737,10.1016/j.apcata.2004.07.030,precipitation_ceramic_synthesis,"To prepare synthetic hydrotalcite, we first dissol ... 500 degC for 16 h to produce Mg(Al)Ox mixed oxide."
5738,10.1016/j.materresbull.2009.06.003,precipitation_ceramic_synthesis,"The layered precursor Co2+Fe2+Fe3+-SO42--LDHs was  ... errite nanoparticle, which was denoted as CoFe2O4."
5739,10.1016/j.cej.2014.10.037,precipitation_ceramic_synthesis,Bi2Fe4O9 nanoparticles were synthesized by a co-pr ... ying in a vacuum freeze dryer (denoted as BFO249).
5740,10.1016/j.jnoncrysol.2011.02.027,precipitation_ceramic_synthesis,ZnWO4 nanoparticles were synthesized using co-prec ... egC. Thus all powders obtained were white-colored.
5741,10.1016/j.jmmm.2011.07.040,precipitation_ceramic_synthesis,"However, Co(1-x)ZnxFe2O4 nanoparticles synthesized ... action vessel to keep the M/OH--ratio around 0.20."
5742,10.1016/j.apcatb.2008.06.006,precipitation_ceramic_synthesis,"ZnAl- and ZnSn-LDHs with the cationic Zn2+/Al3+ an ... T, where T stands for the calcination temperature."
5743,10.1016/j.cattod.2015.09.044,precipitation_ceramic_synthesis,"Cu/ZnO/Al2O3 catalysts were prepared by a modified ... he calcination temperatures of 573, 623 and 673 K."
5744,10.1016/j.cattod.2015.09.006,precipitation_ceramic_synthesis,Zn-Al oxide catalysts were prepared using co-preci ... ed finally by calcining HTlcs at 500 degC for 4 h.
5745,10.1016/j.jcat.2007.08.002,precipitation_ceramic_synthesis,"The nano-composite oxide containing Al2O3, ZrO2, a ...  which showed maximal durability against heat [6]."
5746,10.1016/j.cej.2016.03.105,precipitation_ceramic_synthesis,The support was prepared by coprecipitation method ... 50 degC for 3 h with a heating rate of 3 degC/min.
5747,10.1016/j.cplett.2010.05.024,precipitation_ceramic_synthesis,Gold catalysts were prepared by co-precipitation w ... at a flow rate of 50 mL min-1 at 423 K for 30 min.
5748,10.1016/j.cej.2013.04.039,precipitation_ceramic_synthesis,"The precursors, Zn-Al HTLCs with Zn-Al mole ratio  ... ned at different calcination temperatures for 3 h."
5749,10.1016/j.ssi.2009.02.015,precipitation_ceramic_synthesis,"A method developed in our laboratory involving sep ... led water, and finally dried at 60 degC overnight."
5750,10.1016/j.apcatb.2011.12.012,precipitation_ceramic_synthesis,ZrO2 was prepared by co-precipitation. An appropri ... 00 degC for 20 h and calcined at 500 degC for 5 h.
5751,10.1016/j.apcata.2010.05.041,precipitation_ceramic_synthesis,MgAl2O4 has been prepared by means of a co-precipi ... 16 h at 120 degC and calcined for 7 h at 850 degC.
5752,10.1016/j.jallcom.2015.07.269,precipitation_ceramic_synthesis,"Ni1-xMgxFe2O4 (x = 0, 0.1, 0.3, 0.5, 0.7) nanopart ... h. After drying samples were annealed at 900 degC."
5753,10.1016/j.matchemphys.2009.04.012,precipitation_ceramic_synthesis,"For reference, MgAl2O4 was prepared by the co-prec ... r. The resultant MgAl2O4 is denoted as MgAl2O4-CP."
5754,10.1016/j.molcata.2016.05.013,precipitation_ceramic_synthesis,The catalysts were prepared by the co-precipitatio ... ar furnace after crushed and sieved to 40-60 mesh.
5755,10.1016/j.jallcom.2004.01.008,precipitation_ceramic_synthesis,The precursors Ni1-xCox(OH)2 and Ni0.8Co0.2-yAly(O ... higher temperature for longer time in oxygen flow.
5756,10.1016/j.apcatb.2011.08.024,precipitation_ceramic_synthesis,A CuMgAl HT with molar ratios Mg/Cu = 1 and (Mg +  ... cined at 450 degC overnight and labelled as HTcal.
5757,10.1016/j.apcata.2006.03.052,precipitation_ceramic_synthesis,HT with an Mg/Al ratio of 2 was prepared via co-pr ... cated with their respective synthesis temperature.
5758,10.1016/j.mssp.2015.05.042,precipitation_ceramic_synthesis,"Synthesis of undoped In2O3 and 1.0, 5.0, and 10.0% ...  80degC for 5 h. The expected chemical reaction is"
5759,10.1016/j.apcatb.2016.10.023,precipitation_ceramic_synthesis,"NiAl2O4 (NA) spinel was prepared by co-precipitati ... 00 degC, then calcined at 800 degC for 5 h in air."
5760,10.1016/j.apcata.2003.11.007,precipitation_ceramic_synthesis,Supported Ni/Al mixed oxides are prepared by co-pr ...  degC for 4 h to get supported Ni/Al mixed oxides.
5761,10.1016/j.biortech.2015.01.012,precipitation_ceramic_synthesis,"The CZO nanocomposite was synthesized by co-precip ... ctivate into nanocatalyst (Milenova et al., 2013)."
5762,10.1016/j.apcata.2010.05.005,precipitation_ceramic_synthesis,Zinc aluminate nanoparticles were prepared in aque ...  degC for 4 h to obtain the ZnAl2O4 nanoparticles.
5763,10.1016/j.actamat.2009.06.040,precipitation_ceramic_synthesis,"The Gd2(Zr1-xTix)2O7 (x = 0, 0.1, 0.2, 0.3, 0.4, 0 ... o a disk shape and sintered at 1550 degC for 15 h."
5764,10.1016/j.fuel.2011.10.027,precipitation_ceramic_synthesis,"The mCZA supports, with CZ contents 0, 15, 25, 35, ... %) was loaded in a similar manner described above."
5765,10.1016/j.jmmm.2015.06.087,precipitation_ceramic_synthesis,Nanocrystalline NixCo1-xFe2O4 particles with compo ... e overall chemical reactions can be summarized as:
5766,10.1016/j.cattod.2013.12.043,precipitation_ceramic_synthesis,SO42-/TiO2-ZrO2/1.0 wt%-La3+ was prepared by copre ...  for 4 h at 550 degC to get the targeted catalyst.
5767,10.1016/j.cej.2013.01.034,precipitation_ceramic_synthesis,"The starting materials were Mg(NO3)2*6H2O (Merck,  ...  at 393 K for 12 h and annealed at 1223 K for 8 h."
5768,10.1016/j.cattod.2012.06.015,precipitation_ceramic_synthesis,PrMnO3 catalyst was prepared by following co-preci ...  calcined at 850 degC for 8 h in a muffle furnace.
5769,10.1016/j.spmi.2015.04.013,precipitation_ceramic_synthesis,Co-ferrite nanoparticles were prepared by co-preci ... uid with concentration 1 mg ferrite/ml oleic acid.
5770,10.1016/j.cattod.2013.02.031,precipitation_ceramic_synthesis,"CuZnAl, CuMgAl and Cu-Cr catalysts were prepared b ...  of Cu-Cr sample, the Cu/Cr ratio was equal to 20."
5771,10.1016/j.fuel.2008.04.001,precipitation_ceramic_synthesis,"Hydrotalcites with various Mg/Al molar ratios were ...  were designated as MAH-1, MAH-3, MAH-4 and MAH-6."
5772,10.1016/j.cej.2014.09.092,precipitation_ceramic_synthesis,The Fe3O4 particles were prepared via a modified c ... ied in a vacuum oven at room temperature for 24 h.
5773,10.1016/j.jpowsour.2009.10.088,precipitation_ceramic_synthesis,Precursor powders were produced via co-precipitati ... mentioned by Yoshioka [11] and Shaula et al. [12].
5774,10.1016/j.jcat.2010.07.024,precipitation_ceramic_synthesis,"CexZr1-xO2 (x = 0.2, 0.5, 0.8) oxides were prepare ... C5Z5, C8Z2, where y was the copper loading amount."
5775,10.1016/j.snb.2007.11.003,precipitation_ceramic_synthesis,"A chemical co-precipitation method was used for sy ... al Scanning Electron Microscope, Model JSM-6360A)."
5776,10.1016/j.cej.2009.12.036,precipitation_ceramic_synthesis,Parent Mg/Al-hydrotalcite-like precursor with a mo ... groups [17] and [18]. This sample was called HTr4.
5777,10.1016/j.materresbull.2004.07.003,precipitation_ceramic_synthesis,The LiFePO4 cathode material was prepared by a co- ... ow of nitrogen gas containing 1 vol.% of hydrogen.
5778,10.1016/j.cej.2012.06.152,precipitation_ceramic_synthesis,"Two different coprecipitation methods, low supersa ... hods and thermal activation is given elswere [25]."
5779,10.1016/j.jpcs.2006.01.078,precipitation_ceramic_synthesis,The Mg/Al LDH - NO 3 - was prepared by co-precipit ... ly de-ionic water and dried under vacuum for 24 h.