Comparison of silica-supported MoO3 and V2O5 catalysts in the selective partial oxidation of methane

被引:98
作者
Faraldos, M
Banares, MA
Anderson, JA
Hu, HC
Wachs, IE
Fierro, JLG
机构
[1] UNIV DUNDEE, DEPT CHEM, DUNDEE DD1 4HN, SCOTLAND
[2] LEHIGH UNIV, ZETTLEMOYER CTR SURFACE STUDIES, BETHLEHEM, PA 18015 USA
[3] LEHIGH UNIV, DEPT CHEM ENGN, BETHLEHEM, PA 18015 USA
关键词
D O I
10.1006/jcat.1996.0140
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
Silica-supported molybdenum oxide and vanadium oxide catalysts have been prepared with a wide range of surface metal loadings (0.3-3.5 metal atom/nm(2)), Isolated surface metal oxide species are dominant at surface metal loadings on silica below ca. 1 metal atom/nm(2) while at higher loadings, the metal oxide species tend to aggregate into crystalline MoO3 and V2O5 particles. Both catalyst series have been tested in the selective oxidation of methane with molecular oxygen at atmospheric pressure. The reactivity for methane conversion appears to be essentially related to dispersed isolated surface metal oxide species, with the surface vanadium oxide species being more reactive than molybdenum oxide species. The higher reactivity of the surface vanadium oxide sites may be related to the different nature of the interaction of the oxides with oxygen, Silica-supported vanadium oxide catalysts, despite their higher activity, result in lower yields to HCHO than silica-supported molybdenum oxide catalysts. (C) 1996 Academic Press, Inc.
引用
收藏
页码:214 / 221
页数:8
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