首页 | 本学科首页   官方微博 | 高级检索  
     检索      

用磷-稀土元素改性ZSM-5沸石催化剂的催化特性研究
引用本文:陈连璋,孙多里,王静玉,王祥生.用磷-稀土元素改性ZSM-5沸石催化剂的催化特性研究[J].大连理工大学学报,1986(3).
作者姓名:陈连璋  孙多里  王静玉  王祥生
作者单位:大连工学院基本有机化工教研室 (陈连璋,孙多里,王静玉),大连工学院基本有机化工教研室(王祥生)
摘    要:本文用Hammett指示剂法,程序升温脱附法和红外光谱法考察了磷和磷一(?)改性ZSM-5沸石催化剂表面酸性变化对甲苯歧化催化剂性能影响,认为磷酸与沸石的直接作用,使沸石的强酸中心消失。而磷酸与加入氧化铝担体的ZSM-5沸石催化剂的相互作用,主要表现为变强酸中心为弱酸中心。通过与催化反应结果关联,看出反应选择性的提高与强酸中心和弱酸中心的比值有关。因此,用磷-PK稀土改性ZSM-5沸石催化剂上甲苯歧化,对二甲苯选择性提高到92-96%左右.

关 键 词:催化剂    改性  沸石  稀土族  歧化反应  反应选择性  红外分光光度法/ZSM-5沸石  程序升温脱附法  Hammett指示剂法

An Investigation of Catalytic Character of a ZSM-5 Zeolite Catalyst Modified by Phosphorous-Rare Earth Elements
Chen Lianzhang,Sun Duoli,Wang Jingyu,Wang Xiangsheng.An Investigation of Catalytic Character of a ZSM-5 Zeolite Catalyst Modified by Phosphorous-Rare Earth Elements[J].Journal of Dalian University of Technology,1986(3).
Authors:Chen Lianzhang  Sun Duoli  Wang Jingyu  Wang Xiangsheng
Institution:Chen Lianzhang,Sun Duoli,Wang Jingyu,Wang Xiangsheng Department of Petro-Chemical Engineering,DIT
Abstract:The Hammett indicator, TPD and IR methods are used to study the relation bet- ween the surface acidic properties of a P-La modified ZSM-5 zeolite catalyst and its toluol disproportion catalytic properties. The authors assume that the interaction between phosphoric acid and zeolite causes the disappearance of strong acidic centers. When the alumina carrier is added, the interaction of them causes the change of strong acidic center to weak acidic center. In connection to its catalytic reactivity, the authors find out that there is close relation between the selectivity and the ratio of strong and weak acidic centers. So that the xylene selectivity of toluol disproportion reaction on these ZSM-5 zeolite catalysts modified by phosphorous and rare-earth elements could be increased to 92- 96 %.
Keywords:catalyst  phosphotous  modification  zeolite  rare-earth  dispropor- tion reaction  reaction selectivity  infrared spectrophotometry/ZSM-5 zeolite  TPD  Hammett indicator
本文献已被 CNKI 等数据库收录!
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