In situ electrical conductivity study of titania-supported vanadium-niobium oxide catalysts used in the oxidative dehydrogenation of propane

被引:23
作者
Viparelli, P
Ciambelli, P
Volta, JC
Herrmann, JM
机构
[1] Ecole Cent Lyon, CNRS, URA Photocatalyse Catalyse & Environm, F-69131 Ecully, France
[2] Univ Naples Federico II, Dipartimento Ingn Chim, Naples, Italy
[3] Univ Salerno, Dipartimento Ingn Chim & Alimentaire, Fisciano, Italy
[4] Inst Rech Catalyse, CNRS, F-69626 Villeurbanne, France
关键词
vanadia-niobia; titania support; propane oxydehydrogenation; electrical conductivity; redox processes;
D O I
10.1016/S0926-860X(98)00433-5
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The electrical conductivity of a series of TiO2-supported vanadia-niobia catalysts was measured (i) in pure oxygen to characterize the supported active phases and (ii) in reacting atmospheres to determine their redox properties. In vanadia/titania catalysts, minute amounts of pentavalent V5+ ions were dissolved in the sub-lattice of titania by substitution to Ti4+ sites, the amount increasing proportionally to the loading of vanadia. Similarly, Nb5+ ions also dissolved in the titania sub-lattice, but when niobia were codeposited with vanadia, only V5+ ions dissolved in titania. The variations of the electrical conductivity under oxygen and propane as well as in oxygen-propane mixture showed a redox behavior of the catalysts with the consumption of surface O2- anions during the oxidative dehydrogenation of propane and their replacement by gaseous oxygen. A permanent electron transfer exists from the reduced supported oxidic phase to titania. Niobium sites are not easily reduced and slightly affect the redox properties of vanadium sites which are the active sites, whereas niobium acts as an additive favoring the selectivity to propene. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:165 / 173
页数:9
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