标题:CO2 methanation over TiO2-Al2O3 binary oxides supported Ru catalysts
作者:Xu, Jinghua; Lin, Qingquan; Su, Xiong; Duan, Hongmin; Geng, Haoran; Huang, Yanqiang
通讯作者:Geng, Haoran(mse_genghr@ujn.edu.cn)
作者机构:[Xu, J] School of Materials Science and Engineering, Shandong University, Jinan, 250061, China, State Key Laboratory of Catalysis, Dalian Institute of 更多
会议名称:6th Global Chinese Symposium of Chemical Engineering
会议日期:JUL 16-19, 2014
来源:中国化学工程学报(英文版)
出版年:2016
卷:24
期:1
页码:140-145
DOI:10.1016/j.cjche.2015.07.002
关键词:CO2 methanation;Supported Ru catalyst;TiO2-Al2O3 binary oxide
摘要:TiO2 modified Al2O3 binary oxide was prepared by a wet-impregnation method and used as the support for ruthenium catalyst. The catalytic performance of Ru/TiO2-Al2O3 catalyst in CO2 methanation reaction was investigated. Compared with Ru/Al2O3 catalyst, the Ru/TiO2-Al2O3 catalytic system exhibited a much higher activity in CO2 methanation reaction. The reaction rate over Ru/TiO2-Al2O3 was 0.59 mol CO2.(g Ru)(-1).h(-1), 3.1 times higher than that on Ru/Al2O3 [0.19 mol CO2.(g Ru)(-1).h(-1)]. The effect of TiO2 content and TiO2-Al2O3 calcination temperature on catalytic performance was addressed. The corresponding structures of each catalyst were characterized by means of H-2-TPR, XRD, and TEM. Results indicated that the averaged particle size of the Ru on TiO2-Al2O3 support is 2.8 nm, smaller than that on Al2O3 support of 4.3 nm. Therefore, we conclude that the improved activity over Ru/TiO2-Al2O3 catalyst is originated from the smaller particle size of ruthenium resulting from a strong interaction between Ru and the rutile-TiO2 support, which hindered the aggregation of Ru nanoparticles. (C)c 2015 The Chemical Industry and Engineering Society of China, and Chemical Industry Press. All rights reserved.
收录类别:CPCI-S;EI;CSCD;SCOPUS;SCIE
WOS核心被引频次:8
Scopus被引频次:11
资源类型:会议论文;期刊论文
原文链接:https://www.scopus.com/inward/record.uri?eid=2-s2.0-85027927415&doi=10.1016%2fj.cjche.2015.07.002&partnerID=40&md5=faca88d1d13f6cf38029c1a72bd99e40
TOP