个人信息Personal Information
教授
博士生导师
硕士生导师
主要任职:盘锦校区管委会副主任兼教学与科研工作部部长
性别:男
毕业院校:大连理工大学
学位:博士
所在单位:化工学院
学科:工业催化. 物理化学
办公地点:化工实验楼B427
联系方式:18641143913
电子邮箱:guoxw@dlut.edu.cn
Characterization and catalytic alkylation of hydrothermally dealuminated nanoscale ZSM-5 zeolite catalyst
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论文类型:期刊论文
发表时间:2008-03-15
发表刊物:CATALYSIS COMMUNICATIONS
收录刊物:SCIE、EI
卷号:9
期号:4
页面范围:487-493
ISSN号:1566-7367
关键字:nanoscale ZSM-5 zeolite; hydrothermal treatment; toluene alkylation with methanol; para-Xylene
摘要:The acidity and pore structure of nanoscale ZSM-5 zeolite catalysts with both alumina and rare earth as binders and treated by pure steam were studied by various techniques, including X-ray diffraction (XRD), Ammonia Temperature Programmed Desorption (NH3-TPD), Fourier-transform infrared spectroscopy (FT-IR) of adsorbed pyridine, modified Hammett indicator, Al-27 MAS NMR spectroscopy, low temperature NZ adsorption and adsorption of hexane and cyclohexane. The catalytic performance of the catalysts was investigated using alkylation of toluene with methanol and ethylbenzene with ethanol as probe reactions. The results indicated that the nanoscale ZSM-5 catalysts treated at temperatures up to 800 degrees C maintained good crystallinity. Both the amount of the tetrahedrally coordinated framework aluminum and that of the octahedrally coordinated nonframework aluminum decreased; the average pore diameter increased; and the adsorption capacities for normal hexane and cyclohexane declined on the dealuminated nanoscale ZSM-5 catalyst samples. For the catalyst treated at 700 degrees C, not only the catalytic activity for the alkylation of toluene with methanol was improved, but was the selectivity of para-xylene, although the total acid amount decreased significantly and strong acid sites almost disappeared. The alkylation activity was very low when the hydrothermal treatment temperature was 800 degrees C. Correspondingly, the activity of the catalysts for the alkylation of ethylbenzene with ethanol decreased with elevated treatment temperatures. (C) 2007 Elsevier B.V. All rights reserved.