The role of the support in CO hydrogenation selectivity of supported rhodium
作者
James R. Katzer,A.W. Sleight,P. Gajardo,John B. Michel,Edward F. Gleason,Scott A. McMillan
出处
期刊:Faraday discussions of the Chemical Society [The Royal Society of Chemistry] 日期:1981-01-01卷期号:72: 121-121被引量:150
标识
DOI:10.1039/dc9817200121
摘要
Catalytic hydrogenation of CO offers tremendous challenges in catalyst design to control selectivity because of the large variety of hydrocarbons and oxygen-containing species that can be formed; Rh can produce the full range of potential products. Rh on SiO2, Al2O3, TiO2, CeO2 and MgO has been characterized by a complement of techniques and by CO hydrogenation activity. Catalytic activity varied over 200-fold, dependent on the support; Rh/TiO2 was the most active. Selectivity to alcohols vs. hydrocarbons and to methanol vs. ethanol varied over 50-fold. CO hydrogenation selectivity to alcohols varies with the basicity of the support; MgO, the most basic support, exhibited 90 % selectivity to methanol.