异构化
催化作用
X射线光电子能谱
双功能
戊烷
价(化学)
化学
金属
无机化学
布朗斯特德-洛瑞酸碱理论
己烷
氢
氧化还原
光化学
化学工程
有机化学
工程类
作者
A. Katrib,V. Logie,M. Peter,P. Wehrer,L. Hilaire,G. Maire
出处
期刊:Journal de chimie physique
[EDP Sciences]
日期:1997-01-01
卷期号:94: 1923-1937
被引量:31
标识
DOI:10.1051/jcp/1997941923
摘要
The X.P.S Spectra of MoO2, WO2 and WO3 are presented. It was revealed that these commercial MoO2 and WO2 samples are partially oxidized on the surface to the more stable MoO3 and WO3 states respectively, with the presence of Mo(V) and W(V) in the interfaces. In Situ reduction of these samples, by hydrogen at different temperatures enabled to reduce MoO3 or WO3 to lower oxidation states. Catalytic activities in terms of isomerization reactions of 2-methyl pentane reactant to 3-methyl pentane and n-hexane as major products were interpreted in terms of a bifunctional mechanism involving the two free valence electrons of MoO2 and WO2 (metallic site) and the -OH (Bronsted acidic site) on the sample surface.
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