首页 | 本学科首页   官方微博 | 高级检索  
     

低温晶化对B-ZSM-5和Ti-ZSM-5物化性能的影响
引用本文:刘民,郭新闻,高健,王祥生,刘秀梅,韩秀文,包信和. 低温晶化对B-ZSM-5和Ti-ZSM-5物化性能的影响[J]. 催化学报, 2005, 26(8): 660-664
作者姓名:刘民  郭新闻  高健  王祥生  刘秀梅  韩秀文  包信和
作者单位:大连理工大学精细化工国家重点实验室,辽宁,大连,116012;中国科学院大连化学物理研究所催化基础国家重点实验室,辽宁,大连,116023
基金项目:国家重点基础研究发展计划(973计划);新世纪优秀人才支持计划
摘    要: 以改进方法合成的B-ZSM-5分子筛为母体,采用气固相法合成了Ti-ZSM-5分子筛,并以XRD,FT-IR,UV-Vis,XRF,SEM,ICP-AES和MAS NMR等手段对B-ZSM-5和Ti-ZSM-5进行了表征,考察了Ti-ZSM-5对苯酚羟基化反应的催化性能. 结果表明,合成B-ZSM-5时的前期低温晶化有助于晶粒的减小; 以其为母体制备的Ti-ZSM-5对苯酚羟基化反应具有优异的催化性能. 在n(PhOH)/n(H2O2)=3,n(Me2CO)/n(PhOH)=2.7,m(cat)/m(PhOH)=5%,T=353 K和t=6 h的反应条件下,苯酚转化率可达20%以上.

关 键 词:    ZSM-5分子筛  气固相法  苯酚  羟基化
文章编号:0253-9837(2005)08-0660-05
收稿时间:2004-11-01
修稿时间:2004-11-01

Effect of Low-Temperature Crystallization on Physico-Chemical Properties of B-ZSM-5 and Ti-ZSM-5
LIU Min,GUO Xinwen,GAO Jian,WANG Xiangsheng,Liu Xiumei,HAN Xiuwen,Bao Xinhe. Effect of Low-Temperature Crystallization on Physico-Chemical Properties of B-ZSM-5 and Ti-ZSM-5[J]. Chinese Journal of Catalysis, 2005, 26(8): 660-664
Authors:LIU Min  GUO Xinwen  GAO Jian  WANG Xiangsheng  Liu Xiumei  HAN Xiuwen  Bao Xinhe
Abstract:The Ti-ZSM-5 zeolite samples were successfully synthesized via gas-solid method with B-ZSM-5 zeolite prepared by modified hydrothermal synthesis as precursor. The samples were characterized by XRD, FT-IR, UV-Vis, XRF, SEM, ICP-AES and MAS NMR, and their catalytic performance for hydroxylation of phenol was investigated. The results showed that the crystallization at lower temperature during the synthesis of B-ZSM-5 was advantageous to get smaller crystal size and the Ti-ZSM-5 samples prepared by using B-ZSM-5 with smaller crystal size as precursor showed better performance for hydroxylation of phenol. Under the reaction conditions of n(PhOH) / n(H_2O_2) =3, n(Me_2CO) / n(PhOH) =2.7, m(cat) / m(PhOH) =5%, T=353 K and t=6 h, the phenol conversion was over 20%.
Keywords:boron   titanium   ZSM-5 zeolite   gas-solid method   phenol   hydroxylation
本文献已被 CNKI 维普 万方数据 等数据库收录!
点击此处可从《催化学报》浏览原始摘要信息
点击此处可从《催化学报》下载全文
设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号