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Al-MCM-41介孔分子筛催化对甲酚叔丁基化反应的研究
引用本文:于心玉,刘彩华,程文萍,杨建国,何鸣元. Al-MCM-41介孔分子筛催化对甲酚叔丁基化反应的研究[J]. 燃料化学学报, 2006, 34(6): 757-760
作者姓名:于心玉  刘彩华  程文萍  杨建国  何鸣元
作者单位:华东师范大学化学系,上海市绿色化学与化工过程绿色化重点实验室,上海,200062;华东师范大学化学系,上海市绿色化学与化工过程绿色化重点实验室,上海,200062;华东师范大学化学系,上海市绿色化学与化工过程绿色化重点实验室,上海,200062;华东师范大学化学系,上海市绿色化学与化工过程绿色化重点实验室,上海,200062;华东师范大学化学系,上海市绿色化学与化工过程绿色化重点实验室,上海,200062
摘    要:2-叔丁基对甲酚是一种有机中间体,在有机合成领域中占有重要地位,被广泛应用于表面活性剂、高档酚类抗氧化剂2246和2246-S、紫外线吸收剂UV-326等的生产[1]。特别是近十年来,以抗热老化为特征的功能性高档酚类抗氧化剂在国内外相继问世,它们对于提高聚合物材料的成型加工性能、

关 键 词:HAl-MCM-4介孔分子筛  对甲酚  甲基叔丁基醚  2-叔丁基对甲酚  催化
文章编号:0253-2409(2006)06-0757-04
收稿时间:2006-03-24
修稿时间:2006-06-24

Tert-butylation of p-cresol catalyzed by Al-MCM-41 mesoporous molecular sieves
YU Xin-yu,LIU Cai-hua,CHENG Wen-ping,YANG Jian-guo,HE Ming-yuan. Tert-butylation of p-cresol catalyzed by Al-MCM-41 mesoporous molecular sieves[J]. Journal of Fuel Chemistry and Technology, 2006, 34(6): 757-760
Authors:YU Xin-yu  LIU Cai-hua  CHENG Wen-ping  YANG Jian-guo  HE Ming-yuan
Affiliation:Shanghai Key Laboratory of Green Chemistry and Chemical Process, Chemistry of Department, East China Normal University, Shanghai 200062
Abstract:Mesoporous molecular sieves Al-MCM-41 with n(SiO_2)/n(Al_2O_3) ratio being 20,50 and 100 were prepared.As proved by X-ray diffraction(XRD) patterns and the N_2 physical sorption,the as-synthesized Al-MCM-41 exhibited typical hexagonal structure,large surface areas and narrow pore distribution.The performance of HAl-MCM-41 as catalyst for tert-butylation of p-cresol with methyl tert-butyl-ether(MTBE) was then investigated.The effects of temperature,weight hourly space velocity(WHSV) and the feed ratio n(MTBE)/n(p-cresol) on p-cresol conversion and product selectivity were examined.The results showed that mesoporous HAl-MCM-41 molecular sieves(n(SiO_2)/n(Al_2O_3) = 20) is an efficient catalyst with high activity,selectivity and stability for the synthesis of 2-tert-butyl-p-cresol from p-cresol and MTBE by tert-butylation.
Keywords:mesoporous HAl-MCM-41 molecular sieves  p-cresol  methyl tert-butyl-ether  2-tert-butyl-p-cresol  catalysis
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