KINETIC-STUDIES OF THE ISOMERIZATION OF N-BUTENES OVER BOROALUMINOSILICATE ZEOLITES

被引:29
作者
BIANCHI, D
SIMON, MW
NAM, SS
XU, WQ
SUIB, SL
OYOUNG, CL
机构
[1] UNIV CONNECTICUT, DEPT CHEM ENGN, STORRS, CT 06269 USA
[2] UNIV CONNECTICUT, DEPT CHEM, STORRS, CT 06269 USA
[3] UNIV CONNECTICUT, INST MAT SCI, STORRS, CT 06269 USA
[4] TEXACO USA INC, BEACON, NY 12508 USA
关键词
D O I
10.1006/jcat.1994.1066
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
Boroaluminosilicate zeolites have been used as n-butene isomerization catalysts in this study. Al3+ free boron zeolites are inactive for n-butene isomerization. Spectroscopic and microscopic studies have been used to monitor the structure, thermal stability, and acidity of these materials. Kinetic studies are the main focus of this paper, with an emphasis on determination of the mechanism of n-butene isomerization over boron zeolites. Results show that the reaction is first order in n-butenes with slow deactivation via coke formation. Isobutylene, propylene, and C5-C8 polymeric species are the main products. Comparisons of the activity and selectivity of boroaluminosilicates, Al3+-free B zeolites, and Al3+ is necessary to enhance yields of isobutylene. A two-step model is proposed to account for product selectivity, deactivation, and observed kinetic data. © 1994 Academic Press, Inc.
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页码:551 / 560
页数:10
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