首页|苯与环戊烯烷基化制备环戊基苯的工艺研究

苯与环戊烯烷基化制备环戊基苯的工艺研究

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以苯和环戊烯为原料,采用固定床工艺通过烷基化反应合成环戊基苯,考察了不同结构催化剂的烷基化活性,并探讨了苯/环戊烯质量比、体积空速、反应温度、反应压力等对环戊烯转化率和环戊基苯选择性的影响.结果表明:催化剂对苯/环戊烯烷基化反应影响较大,孔道尺寸和酸性质均适宜的介孔沸石分子筛催化剂更适合催化苯/环戊烯烷基化制备环戊基苯;适当提高苯/环戊烯质量比、反应温度及降低反应空速、反应压力有利于烷基化反应向正反应方向进行,减少副反应发生;选择介孔沸石分子筛催化剂,在原料苯/环戊烯质量比8:1,体积空速3 h-1,反应温度180℃,反应压力2.0 MPa的条件下合成环戊基苯,环戊烯的转化率较高,为 99.8%,环戊基苯的选择性为 92.2%.
Preparation of cycloamyl benzene by alkylation of benzene and cyclopentene
Using benzene and cyclohexene as raw materials,cyclopentyl benzene was synthesized through alkylation reaction using a fixed bed process.The alkylation activity of catalysts with different structures was investigated.And the effects of ben-zene/cyclopentene mass ratio,volume space velocity,reaction temperature,reaction pressure,etc.,on the conversion rate of cyclopentene and the selectivity of cyclopentyl benzene were investigated.The results showed that catalysts had a significant impact on the alkylation reaction of benzene/cyclopentene,and mesoporous zeolite molecular sieve catalysts with rational pore size and acidity were more suitable for catalyzing the alkylation of benzene/cyclopentene to prepare cyclopentyl benzene;properly increasing the mass ratio of benzene/cyclohexene and reaction temperature and reducing reaction space velocity and reaction pres-sure helped the alkylation reaction proceed in the positive direction and reduce the occurrence of side reactions;and the conver-sion rate of cyclopentene was as high as 99.8%and the selectivity of cyclopentyl benzene was 92.2%when cyclopentyl benzene was synthesized by selecting mesoporous zeolite molecular sieve catalyst under the conditions of benzene/cyclohexene mass ratio of 8:1,volum space velocity of 3 h-1,reaction temperature of 180℃ and reaction pressure of 2.0 MPa.

benzenecyclopentenecyclopentyl benzene alkylationmesoporous zeolite molecular sieve

邓金中、吴明

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中石化湖南石油化工有限公司聚酰胺部,湖南 岳阳 414007

环戊烯 环戊基苯 烷基化 介孔沸石分子筛

中石化股份有限公司研究项目

202223Z01

2024

合成纤维工业
中国石化集团巴陵石油化工有限责任公司 中国石化集团公司合成纤维科技情报中心站

合成纤维工业

CSTPCD
影响因子:0.417
ISSN:1001-0041
年,卷(期):2024.47(4)
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