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LiAgSO4-Al2O3复合电解质的导电性研究 总被引:6,自引:0,他引:6
研究了分散第二相α-Al2O3对LiAgSO4的离子导电性的影响,发现LiAgSO4-Al2O3的电导率随a-Al2O3含量的增加而升高,在300-500℃间电导率高于纯LiAgSO4,a-Al2O3含量摩尔比约为40时最高。TG-DTA和XRD分析表明,在高温稳定的体立心LiAgSO4降温后以Ag2SO4的正交β相形式存在,但在H2O存在下,生成Li2SO4.H2O和Ag2SO4.FT-IR分析 相似文献
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CrO3.CH3NH2.HCl/Al2O3的制备及其对苯偶姻体系的氧化反应 总被引:1,自引:0,他引:1
CrO3·CH3NH2·HCl/Al2O3的制备及其对苯偶姻体系的氧化反应张贵生*石启增陈密峰蔡昆(河南师范大学化学系新乡453002)关键词CrO3·CH3NH2·HCl/Al2O3,苯偶姻,苯偶酰,氧化1996-08-18收稿,1996-11-0... 相似文献
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在色谱微反流动法实验装置上考察了负载Sm2O3对CuOγAl2O3催化剂CO氧化活性的影响,并运用X射线衍射(XRD)、程序升温还原(TPR)及程序升温脱附(TPDMS)技术研究了Sm2O3对CuOγAl2O3催化剂的物相结构、氧化还原特性及表面氧的脱附与恢复行为的影响。结果表明,负载适量的Sm2O3对CuOγAl2O3催化剂表面氧的脱出与恢复有促进作用,可使部分γAl2O3相变成γAl2O3和θAl2O3的混合型。负载适量的Sm2O3能改善催化活性,而负载过量的Sm2O3则使CuO催化剂上CuO的晶粒增大,从而对催化活性起了抑制作用。 相似文献
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(Y(NTO)2NO3(H2O)5).2H2O的制备,晶体结构和热分解机理的… 总被引:4,自引:0,他引:4
合在了(Y(NTO)2NO3(H2O)5).2H2O(NTO为3-硝基-1,2,4-三唑-5-酮)并测定了晶体结构,晶体属单斜晶系,空间群Cm,晶胞参数:a=0.6773(2)nm,b=2.0866(2)nm,c=0.6551(1)nm;β=102.98(2)°V=0.9021(1)nm^3,Z=2,Dc=1.970g.cm^-3,μ=33.49cm^-1,F(000)=540,R=0.032,中 相似文献
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Zusammenfassung Durch Wegkochen von NH3 aus ammoniakalischen Tartratlösungen des As2O3 und Sb2O3 in verschiedenem Verhältnis wurden einerseits monokline Mischkristalle der Oxyde mit einem Gehalt zwischen 100 und 70 Molprozent Arsen, andererseits kubische Mischkristalle mit 30 bis 100 Molprozent Antimon gewonnen. Die analytischen Ergebnisse werden durch Röntgen- und Infrarot-Untersuchungen bestätigt, aus den letzteren ergeben sich weitere Hinweise auf die Struktur.Mit 1 Abbildung1. Mitt.:E. Hayek, M. Hohenlohe-Profanter, B. Marcic undE. Beetz, Angew. Chem.70 307 (1958). 相似文献
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以AlCl3 为络合物配体, 研究Sm2O3Eu2O3Gd2O3 的分离特性。结果表明, 其传输能力为:Sm ≈Gd> Eu, 氯化物主要在980 ~1100 K 沉积。不同温区的最大分离系数分别为: βEu/Sm;1200 K= 1-70 ,βEu/Gd;1300 K= 1-88 , βSm/Gd;1300 K = 1-24 , β′Sm/Eu;850 ~880 K= 2-76 , β′Gd/Eu;880~900 K = 2-83 , β′Gd/Sm;800 K=1-12 , 高于传统的湿法分离系数。 相似文献
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Aleksey A. Yaremchenko Vladislav V. Kharton Evgeny N. Naumovich Anneta A. Tonoyan Viktor V. Samokhval 《Journal of Solid State Electrochemistry》1998,2(5):308-314
Electrical conductivity, fluorite-type cubic unit cell volume and thermal expansion of the (Bi1−
x
Nb
x
)1−
y
Ho
y
O1.5+δ (x=0.05 and 0.08; y=0.10−0.15) and (Bi1−
x
Zr
x
)1−
y
Y
y
O1.5+δ (x=0.05 and 0.07; y=0.15) solid solutions have been found to decrease regularly with increasing dopant content. Annealing at temperatures below
900 K leads to a phase decomposition and to a sharp decrease in conductivity of the ceramics. Oxygen ion transference numbers
have been determined by the e.m.f. method and by Faradaic efficiency measurement to exceed 0.9. A new technique of studying
Faradaic efficiency has been proposed and verified using (Bi0.95Zr0.05)0.85Y0.15O1.5+δ and Zr0.90Y0.10O1.95 ceramic samples.
Received: 31 October 1997 / Accepted: 18 December 1997 相似文献
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The density and surface tension of melts of the systems CaO-FeO-Fe2O3 MgO at the temperature 1623 K, CaO-FeO-Fe2O3-ZnO at 1573 K, and CaO-Fe2O3-Cu2O at 1573 K were determined using the maximum bubble pressure method. The molar volume, the excess molar volume, and the excess
surface tension were calculated on the basis of the obtained data. From these properties information on the interactions of
components and possible chemical reactions between them was obtained. Due to the absence of silica and the low concentration
of other network-forming oxides, only isolated FeO
4
5−
tetrahedra and the CaO·FeO ionic pairs are formed in these basic melts, the donor of the oxygen atoms being either CaO, FeO,
or both CaO+FeO oxides. Even the observed ternary interactions may be attributed to the formation of the anions FeO
4
5−
only. 相似文献
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Y2O3, La2O3, Sm2O3对氧化铝瓷烧结及力学性能的影响 总被引:16,自引:3,他引:16
研究了3种稀土氧化物对氧化铝陶瓷烧结性能和力学性能的影响.结果表明 含Y2O3,La2O3,Sm2O3的添加剂促进了氧化铝瓷的烧结,提高了氧化铝瓷的力学性能.Y2O3和Sm2O3掺量为0.50%,La2O3掺量为0.75%时氧化铝瓷在1600或1620 ℃保温2 h烧结,相对密度达98.9%以上,强度超过439 MPa,断裂韧性达5.15 MPa·m1/2以上.微观结构分析表明,Y2O3,La2O3,Sm2O3抑止氧化铝晶粒生长,细化晶粒,使晶粒尺寸较均匀形成致密化结构. 相似文献
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The effect of ferric and manganese oxides dopants on thermal and physicochemical properties of Mn-oxide/Al2O3 and Fe2O3/Al2O3 systems has been studied separately. The pure and doped mixed solids were thermally treated at 400–1000°C. Pyrolysis of pure
and doped mixed solids was investigated via thermal analysis (TG-DTG) techniques. The thermal products were characterized
using XRD-analysis. The results revealed that pure ferric nitrate decomposes into Fe2O3 at 350°C and shows thermal stability up to1000°C. Crystalline Fe3O4 and Mn3O4phases were detected for some doped solids precalcined at 1000°C. Crystalline γ-Al2O3 phase was detected for all solids preheated up to 800°C. Ferric and manganese oxides enhanced the formation of α-Al2O3 phase at1000°C. Crystalline MnAl2O4 and MnFe2O4 phases were formed at 1000°C as a result of solid–solid interaction processes. The catalytic behavior of the thermal products
was tested using the decomposition of H2O2 reaction.
This revised version was published online in August 2006 with corrections to the Cover Date. 相似文献