Hydroalkylation of Benzene and Methylbenzenes

Y. Yamazaki, A. Masuda, T. Kawai, S. Kimura
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引用次数: 3

Abstract

A series of nickel catalysts supported on silica-alumina was prepared for hydroalkylation of aromatic hydrocarbons and effects of pretreatment of catalysts and reaction conditions on their catalytic activity were studied. The selectivity of cyclohexylbenzene which is obtained by hydroalkylation of benzene correlated to the surface acidity of silica-alumina support. The most suitable catalyst was nickel (3∼5wt%) supported on silica-alumina (alumina content: ca. 42wt%), and the results obtained with this simple catalyst were compared with those obtained with catalyst of nickel on a silica-alumina carrier containing both tungsten and fluorine reported by Slaugh et al.The molar ratio of cyclohexylmethylbenzenes to cyclohexylbenzene formed by the reaction of equimolar mixture of benzene and methylbenzenes increased with increase in the basicity of the methylbenzenes.
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苯和甲苯的氢烷基化反应
制备了一系列用于芳烃氢烷基化反应的硅铝负载镍催化剂,研究了催化剂预处理和反应条件对其催化活性的影响。通过苯的加氢烷基化反应得到的环己基苯的选择性与二氧化硅-氧化铝载体的表面酸度有关。最合适的催化剂是二氧化硅-氧化铝负载的镍(3 ~ 5wt%)(氧化铝含量:用这种简单催化剂与Slaugh等在含钨氟硅-氧化铝载体上用镍催化剂的反应结果进行了比较。苯和甲苯的等摩尔混合物反应生成的环己基甲基苯与环己基苯的摩尔比随着甲苯碱度的增加而增加。
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