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
相关论文
共 33 条
[1]  
Argauer R.J., 1972, US Pat., Patent No. [3702886, US3702886A]
[2]   As to the reasons of the high activity of a commercial pentasil-type zeolite in the vapor-phase Fries rearrangement [J].
Borzatta, V ;
Busca, G ;
Poluzzi, E ;
Rossetti, V ;
Trombetta, M ;
Vaccari, A .
APPLIED CATALYSIS A-GENERAL, 2004, 257 (01) :85-95
[3]   A new vapour phase process to produce 2-hydroxyphenylalkylketones [J].
Borzatta, V ;
Poluzzi, E ;
Vaccari, A .
SCIENCE AND TECHNOLOGY IN CATALYSIS 2002, 2003, 145 :439-442
[4]   NMR AND IR STUDIES OF ZEOLITE H-ZSM-5 MODIFIED WITH ORTHOPHOSPHORIC ACID [J].
CARO, J ;
BULOW, M ;
DEREWINSKI, M ;
HABER, J ;
HUNGER, M ;
KARGER, J ;
PFEIFER, H ;
STOREK, W ;
ZIBROWIUS, B .
JOURNAL OF CATALYSIS, 1990, 124 (02) :367-375
[5]  
Chang C.D., 1975, U.S. Patent, Patent No. 3928483
[6]  
CHENG CC, 1977, J CATAL, V47, P249
[7]  
Dworezkow G., 1985, STUD SURF SCI CATAL, V21, P163
[8]   Acylation of aromatic compounds on H-Beta zeolites [J].
Freese, U ;
Heinrich, F ;
Roessner, F .
CATALYSIS TODAY, 1999, 49 (1-3) :237-244
[9]   Fast and efficient synthesis of ZSM-5 in a broad range of SiO2/Al2O3 without using seeding gel [J].
Ghiaci, M ;
Seyedeyn-Azad, F ;
Kia, R .
MATERIALS RESEARCH BULLETIN, 2004, 39 (09) :1257-1264
[10]   Investigation of thermodynamic parameters of cetyl pyridinium bromide sorption onto ZSM-5 and natural clinoptilolite [J].
Ghiaci, M ;
Kia, R ;
Kalbasi, RJ .
JOURNAL OF CHEMICAL THERMODYNAMICS, 2004, 36 (02) :95-100