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

预处理方法对Ru/SBA-15催化丙三醇氢解反应性能的影响(英)
引用本文:李宇明,马兰,刘会敏,贺德华.预处理方法对Ru/SBA-15催化丙三醇氢解反应性能的影响(英)[J].催化学报,2014,35(5):677-683.
作者姓名:李宇明  马兰  刘会敏  贺德华
作者单位:a 清华大学化学系, 有机光电子与分子工程教育部重点实验室, 北京100084;
b 防化指挥工程学院, 北京102205
基金项目:国家自然科学基金(20973098,21033004);清华大学分析测试基金.
摘    要:使用浸渍法结合不同预处理方法制备了一系列的Ru/SBA-15催化剂,并将其应用于丙三醇氢解反应中.使用N2吸附-脱附、X射线衍射、CO化学吸附以及透射电子显微镜等方法对所制备Ru/SBA-15进行了表征.结果表明,催化剂前驱体经过空气焙烧后再经H2还原的Ru/SBA-15催化剂上Ru的分散度较低,而直接使用H2处理较高.同时,随着H2还原温度提高,Ru分散度逐渐降低.保持反应活性接近时,随着Ru分散度的降低,TOF增加.表明Ru/SBA-15催化剂上丙三醇氢解是结构敏感反应.

关 键 词:  负载型催化剂  丙三醇  氢解反应  预处理  结构敏感反应
收稿时间:2013-11-16

Influence of pretreatment on the catalytic performance of Ru/SBA-15 catalysts for glycerol hydrogenolysis
Yuming Li,Lan Ma,Huimin Liu,Dehua He.Influence of pretreatment on the catalytic performance of Ru/SBA-15 catalysts for glycerol hydrogenolysis[J].Chinese Journal of Catalysis,2014,35(5):677-683.
Authors:Yuming Li  Lan Ma  Huimin Liu  Dehua He
Institution:a Key Laboratory of Organic Optoelectronics &Molecular Engineering of Ministry of Education, Department of Chemistry, Tsinghua University, Beijing 100084, China;
b Institute of Chemical Defence, Beijing 102205, China
Abstract:Ru/SBA-15 catalysts were prepared by impregnation and were pretreated under different conditions, and were characterized by N2 adsorption-desorption, X-ray diffraction, CO chemisorption, transmission electron microscopy, and the reaction of glycerol hydrogenolysis. The catalyst calcined in air had larger Ru particles, while the direct reduction of the catalysts with H2 without air pre-calcination made the Ru particles dispersed well. As the H2 reduction temperature increased, the Ru dispersion decreased. The turnover frequency (TOF) of the catalysts increased as the Ru dispersion decreased, indicating that Ru/SBA-15 catalyzed glycerol hydrogenolysis is a structure sensitive reaction.
Keywords:Ruthenium  Supported catalyst  Glycerol  Hydrogenolysis  Pretreatment  Structure sensitive reaction
本文献已被 CNKI 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》下载免费的PDF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