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Active sites in CO2 hydrogenation over confined VOx-Rh catalysts 被引量:5
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作者 Guishuo Wang Ran Luo +6 位作者 Chengsheng Yang Jimin Song Chuanye Xiong Hao Tian Zhi-Jian Zhao Rentao Mu Jinlong Gong 《Science China Chemistry》 SCIE EI CAS CSCD 2019年第12期1710-1719,共10页
Metal oxide-promoted Rh-based catalysts have been widely used for CO2 hydrogenation,especially for the ethanol synthesis.However,this reaction usually suffers low CO2 conversion and alcohols selectivity due to the for... Metal oxide-promoted Rh-based catalysts have been widely used for CO2 hydrogenation,especially for the ethanol synthesis.However,this reaction usually suffers low CO2 conversion and alcohols selectivity due to the formation of byproducts methane and CO.This paper describes an efficient vanadium oxide promoted Rh-based catalysts confined in mesopore MCM-41.The Rh-0.3VO/MCM-41 catalyst shows superior conversion(〜12%)and ethanol selectivity(〜24%)for CO2 hydrogenation.The promoting effect can be attributed to the synergism of high Rh dispersion by the confinement effect of MCM-41 and the formation of VOr-Rh interface sites.Experimental and theoretical results indicate the formation of til-CO at VOv-Rh interface sites is easily dissociated into*CH X,and then*CH X can be inserted by CO to form CH3,*CO followed by CH3*CO hydrogenation to ethanol. 展开更多
关键词 interfacial active sites CO2 hydrogenation ETHANOL Rh-based catalysts confined catalysts
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