Internal versus external surface active sites in ZSM-5 zeolite -: Part 1.: Fries rearrangement catalyzed by modified and unmodified H3PO4/ZSM-5

被引:26
作者
Ghiaci, M [1 ]
Abbaspur, A [1 ]
Kalbasi, RJ [1 ]
机构
[1] Isfahan Univ Technol, Dept Chem, Esfahan 84156, Iran
关键词
files rearrangement; cationic surfactant; H(3)PO(4); modified ZSM-5; phenylacetate; 4-hydroxyacetophenone;
D O I
10.1016/j.apcata.2005.09.015
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 Fries rearrangement of phenylacetate has been studied in the vapor-phase at 623 K over a series of surface modified and unmodified ZSM-5 (Si/Al = 60-170) loaded with H(3)PO(4), differing in the external surface treatment of the zeolites. When the external surface of the zeolite is blocked with a surfactant before loading it with H(3)PO(4), the selectivity to form the 4-hydroxyacetophenone was higher. This superior performance of the externally blocked catalysts, relative to the unmodified H(3)PO(4)/ZSM-5 catalyst, shows that by blocking the external surface area of the ZSM-5 support, it exhibits a superior catalytic selectivity than the unmodified catalyst. Catalysts containing 0-4.9 wt.% P were prepared using modified and unmodified ZSM-5 zeolites, and their catalytic performance for vapor-phase Fries rearrangement of phenylacetate to 2-hydroxyacetophenone (2-HAP), 4-hydroxyacetophenone (4-HAP) and 4-acetoxyacetophenone (4-AAP) was determined. The influence of the operating parameters on the performance of H(3)PO(4)/ZSM-5-surf catalysts was also investigated. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 39
页数:8
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