Effects of pretreatment and reduction on the Co/Al_2O_3 catalyst for CO hydrogenation  

Effects of pretreatment and reduction on the Co/Al_2O_3 catalyst for CO hydrogenation

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作  者:Xiaoping Dai Changchun Yu 

机构地区:[1]The Key Laboratory of Catalysis, China National Petroleum Corporation, China University of Petroleum, Beijing 102249, China

出  处:《Journal of Natural Gas Chemistry》2008年第3期288-292,共5页天然气化学杂志(英文版)

基  金:The National Basic Research Program of China (973 Program) (No. 2005CB221402);China National Petroleum Corporation

摘  要:The purpose of this study was to investigate the effect of preadsorbed CO at different temperatures, calcination temperatures, the combined influence of reduction temperature and time, and pretreatment using hydrogen or syngas as reduction agents on the F-T synthesis (FTS) activity and selectivity of Co/Al2O3 catalyst. The reactivity of the carbon species at higher preadsorption temperature with H2 in TPSR decreased, whereas the carbon-containing species showed higher reactivity over Co/Al2O3 catalyst with low calcination temperature. This agreed well with the order of catalytic activity for F-T synthesis on this catalyst. The catalytic activity of the catalyst varied with reduction temperature and time remarkably. CODEX optimization gave an optimum reduction temperature of 756 K and reduction time of 6.2 h and estimated C5+ yield perfectly. The pretreatment of Co/Al2O3 catalyst with different reduction agents (hydrogen or syngas) showed important influences on the catalytic performance. A high CO conversion and C5+ yield were obtained on the catalyst reduced by hydrogen, whereas methane selectivity on the catalyst reduced by syngas was much higher than that on the catalyst reduced by hydrogen.The purpose of this study was to investigate the effect of preadsorbed CO at different temperatures, calcination temperatures, the combined influence of reduction temperature and time, and pretreatment using hydrogen or syngas as reduction agents on the F-T synthesis (FTS) activity and selectivity of Co/Al2O3 catalyst. The reactivity of the carbon species at higher preadsorption temperature with H2 in TPSR decreased, whereas the carbon-containing species showed higher reactivity over Co/Al2O3 catalyst with low calcination temperature. This agreed well with the order of catalytic activity for F-T synthesis on this catalyst. The catalytic activity of the catalyst varied with reduction temperature and time remarkably. CODEX optimization gave an optimum reduction temperature of 756 K and reduction time of 6.2 h and estimated C5+ yield perfectly. The pretreatment of Co/Al2O3 catalyst with different reduction agents (hydrogen or syngas) showed important influences on the catalytic performance. A high CO conversion and C5+ yield were obtained on the catalyst reduced by hydrogen, whereas methane selectivity on the catalyst reduced by syngas was much higher than that on the catalyst reduced by hydrogen.

关 键 词:CO hydrogenation Co/Al2O3 catalyst CO adsorption H2-TPSR surface carbon species reduction condition PRETREATMENT 

分 类 号:TE624.4[石油与天然气工程—油气加工工程]

 

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