Adsorption and reaction of CO2 on Mo2C catalyst

被引:42
|
作者
Solymosi, F [1 ]
Oszkó, A [1 ]
Bánsági, T [1 ]
Tolmacsov, P [1 ]
机构
[1] Univ Szeged, Inst Solid State & Radiochem, React Kinet Res Grp, Hungarian Acad Sci, H-6701 Szeged, Hungary
来源
JOURNAL OF PHYSICAL CHEMISTRY B | 2002年 / 106卷 / 37期
关键词
D O I
10.1021/jp0203696
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 reaction between CO2 and ZSM-5- and SiO2-supported Mo2C catalysts, found to be active in the aromatization of methane, has been studied in a flow and static system by measuring changes in the gas composition. The reaction was also followed with X-ray photoelectron spectroscopy. The decomposition of CO2 occurred above 823 K to give CO and O atoms. Using (CO2)-C-13 it was possible to establish that a fraction of O atoms oxidized the carbon of Mo2C into CO, the other, part reacted with Mo to give MoOx species. The ratio of (CO)-C-13/(CO)-C-12 varied between 5 and 6.0. XPS study confirmed the oxidation of Mo resulting in the formation of Mo ions of various oxidation states. Although the dominant oxidation state is Mo6+ at every temperature, Mo4+ and Mo5+ were present in the sample even after the reaction at 1073 K. The reaction proceeded at a faster rate on Mo2C/ZSM-5 than on Mo2C/SiO2.
引用
收藏
页码:9613 / 9618
页数:6
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