期刊文献+

MCM-56分子筛催化苯与丙烯液相烷基化反应性能 被引量:2

Catalytic Performance of MCM-56 Molecular Sieve for Benzene Alkylation with Propylene
下载PDF
导出
摘要 在晶化釜内动态水热合成了MCM-56分子筛,采用过氧化氢回流处理方法脱除模板剂,获得了高比表面积分子筛MCM-56[MCM-56(H2O2)].采用XRD,N2气吸附-脱附,NH3-TPD和FTIR等对其结构和酸性进行表征,考察了HMCM-56(H2O2)分子筛在苯与丙烯液相烷基化合成异丙苯中的催化性能.研究结果表明,过氧化氢回流处理能够有效去除模板剂.与焙烧去除模板剂的HMCM-56(C)相比,HMCM-56(H2O2)分子筛的BET比表面积达到563m2/g,外表面积提高近2倍.酸性表征说明,与HMCM-56(C)相比,HMCM-56(H2O2)的总酸量较高而酸强度分布不变.在苯与丙烯液相烷基化反应中,HMCM-56(H2O2)分子筛表现出更好的低温活性和更高的异丙苯选择性. MCM-56 zeolite was prepared by hydrothermally dynamic method. The as-made MCM-56 was detemplated by treating with a 30% H2O2 solution to obtain MCM-56 (H2O2) zeolite instead of being treated with high-temperature calcination. The structure and acid properties of samples were studied by means of XRD, N2 adsorption-desorption, NH3-TPD and FTIR. The BET surface area of MCM-56(H2O2) can be improved significantly by hydrogen peroxide detemplation. A higher external surface area of 301 cm^2/g was obtained for HMCM-56(H2O2) compared with 134 cm^2/g for HMCM-56(C). The amount of acid sites has been increased by hydrogen peroxide treatment, while the acid strength has not been modified. Both the HMCM-56 zeolite detemplated by H2O2 and by calcination were used in benzene alkylation with propylene in liquid phase. Under our operation condition, HMCM-56 (H2O2) shows a relative high activity and selectivity to cumene than HMCM-56 (C) , especially under a relative low reaction temperature and benzene-to-propylene molar ratio.
出处 《高等学校化学学报》 SCIE EI CAS CSCD 北大核心 2009年第7期1380-1385,共6页 Chemical Journal of Chinese Universities
基金 吉林省科技厅科技发展计划项目(批准号:20080310) 吉林省教育厅"十一五"科学技术研究项目(批准号:吉教科合字[2008]第180号) 中国博士后科学基金面上资助
关键词 MCM-56分子筛 烷基化 异丙苯 过氧化氢 MCM-56 molecular sieve Alkylation Cumene Hydrogen peroxide
  • 相关文献

参考文献1

  • 1Yu Zhang,Haijun Xing,Piaoping Yang,Peng Wu,Mingjun Jia,Jiazhong Sun,Tonghao Wu. Alkylation of benzene with propylene over MCM-36: A comparative study with MCM-22 zeolite synthesized from the same precursors[J] 2007,Reaction Kinetics and Catalysis Letters(1):45~52

同被引文献12

引证文献2

二级引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部