Transient kinetic analysis of the oxidative dehydrogenation of propane

被引:56
作者
Creaser, D
Andersson, B
Hudgins, RR [1 ]
Silveston, PL
机构
[1] Univ Waterloo, Dept Chem Engn, Waterloo, ON N2L 3G1, Canada
[2] Chalmers Univ Technol, Dept Chem React Engn, S-41296 Gothenburg, Sweden
[3] Lulea Univ Technol, S-97187 Lulea, Sweden
基金
加拿大自然科学与工程研究理事会;
关键词
propane oxidative dehydrogenation; V-Mg-O; transient analysis;
D O I
10.1006/jcat.1998.2336
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
Oxidative dehydrogenation of propane was studied using various transient techniques. Results support a redox mechanism in which propane reduces the catalyst, which is reoxidized by gas-phase oxygen. Only lattice oxygen participates in propene formation. Desorbable oxygen is a major source of poor selectivity, although lattice oxygen also causes total oxidation. Consequently, propene selectivity in the absence of gas-phase O-2 is superior to co-feed, steady-state selectivity at the same propane conversion. Propene selectivity is further improved by increasing the degree of catalyst reduction. (C) 1999 Academic Press.
引用
收藏
页码:264 / 269
页数:6
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