Alkylation of phenol with tertiary butyl alcohol over zeolites

被引:70
作者
Krishnan, AV [1 ]
Ojha, K [1 ]
Pradhan, NC [1 ]
机构
[1] Indian Inst Technol, Dept Chem Engn, Kharagpur 721302, W Bengal, India
关键词
D O I
10.1021/op010077n
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Alkylation of phenol was carried out with tert-butyl alcohol (TBA) producing p-tert-butyl phenol over a variety of zeolite catalysts, namely, zeolite Beta, 13X zeolite, Ce-exchanged 13X zeolite, and zeotite prepared from fly ash. Zeolite Beta showed the highest activity for the reaction under otherwise identical conditions. The activity of 13X zeolite was found to increase with an increase in cerium content in the catalyst, which was accomplished through ion exchange. The activity of zeolite (obtained from fly ash by hydrothermal treatment) in catalyzing the reaction was tested with highly encouraging results. The effects of various parameters such as reaction temperature, reactant ratio (mole ratio of phenol to that of tert-butyl alcohol), and catalyst loading on the rate of reaction were also studied. The alkylation reaction was found to be surface-reaction controlled with negligible interparticle mass-transfer resistance.
引用
收藏
页码:132 / 137
页数:6
相关论文
共 16 条
[1]   ALKYLATION OF PHENOL WITH MTBE AND OTHER TERT-BUTYL ETHERS - CATION-EXCHANGE RESINS AS CATALYSTS [J].
CHANDRA, KG ;
SHARMA, MM .
CATALYSIS LETTERS, 1993, 19 (04) :309-317
[2]   ALKYLATION OF PHENOL WITH ALPHA-METHYLSTYRENE, PROPYLENE, BUTENES, ISOAMYLENE, 1-OCTENE, AND DIISOBUTYLENE - HETEROGENEOUS VS HOMOGENEOUS CATALYSTS [J].
CHAUDHURI, B ;
SHARMA, MM .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1991, 30 (01) :227-231
[3]  
CROZAT MC, 1982, CHEM ABSTR 142455, V96
[4]  
ISAGULYANTS VI, 1957, GAZ PROM IM GUBKINA, V24, P286
[5]  
LYSENKO AP, 1975, CHEM ABSTR 27778, V83
[6]  
MACHO V, 1981, CHEM ABSTR 16891, V95
[7]  
Ojha K, 2001, INDIAN J ENG MATER S, V8, P100
[8]   ALKYLATION OF PHENOL AND PYROCATECHOL BY ISOBUTYL ALCOHOL USING SUPERACID CATALYSTS [J].
RAJADHYAKSHA, RA ;
CHAUDHARI, DD .
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH, 1987, 26 (07) :1276-1280
[9]  
SARTORI G, 1985, CHEM IND, V22, P762
[10]  
Scheriesheism A., 1964, FRIEDEL CRAFTS REL 1, V2, P477