Liquid-phase Beckmann rearrangement of cyclohexanone oxime over mesoporous molecular sieve catalysts

被引:53
|
作者
Ngamcharussrivichai, C
Wu, P
Tatsumi, T
机构
[1] Yokohama Natl Univ, Grad Sch Engn, Div Mat Sci & Chem Engn, Yokohama, Kanagawa 2408501, Japan
[2] Univ Tokyo, Grad Sch Engn, Dept Appl Chem, Bunkyo Ku, Tokyo 1138656, Japan
关键词
Beckmann rearrangement; acidity; mesoporous molecular sieves; benzonitrile;
D O I
10.1016/j.jcat.2004.08.008
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
A series of mesoporous molecular sieves with various SiO2/Al2O3 ratios have been applied to the liquid-phase Beckmann rearrangement of cyclohexanone oxime. The influences of solvent, aluminum content, aluminum-incorporating method, and catalyst structure on the catalytic performance have been investigated. Benzonitrile has been found to be a suitable solvent. The surface silanol groups ineffectively catalyze the rearrangement, whereas the acid sites generated by incorporation of aluminum improve the activity and the selectivity to epsilon-caprolactam remarkably. Moreover, an Al-containing MCM-41 catalyst prepared by the postsynthetic method using AlCl3 as an aluminum precursor exhibits higher lactam selectivity than a directly synthesized one. For a given aluminum content, MCM-41 shows superior performance to beta zeolite and other mesoporous catalysts, SBA-1 and SBA-15. It has been suggested that a sufficient amount of acid sites with appropriate strength is of importance to the liquid-phase Beckmann rearrangement. (C) 2004 Elsevier Inc. All rights reserved.
引用
收藏
页码:448 / 458
页数:11
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