Conversion of CO2 over a Co-Based Fischer-Tropsch Catalyst

被引:33
|
作者
Chakrabarti, Debanjan [1 ]
de Klerk, Arno [1 ]
Prasad, Vinay [1 ]
Gnanamani, Muthu Kumaran [2 ]
Shafer, Wilson D. [2 ]
Jacobs, Gary [2 ]
Sparks, Dennis E. [2 ]
Davis, Burtron H. [2 ]
机构
[1] Univ Alberta, Dept Chem & Mat Engn, Edmonton, AB T6G 2V4, Canada
[2] Univ Kentucky, Ctr Appl Energy Res, Lexington, KY 40511 USA
关键词
COBALT; CARBON; HYDROCARBONS; HYDROGENATION; DEACTIVATION; MECHANISM; KINETICS; ALUMINA;
D O I
10.1021/ie503496m
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The conversion of CO2 over a CoPt/Al2O3 catalyst was investigated. Single-gas adsorption studies indicated that carbon was deposited on the catalyst by exposure to both CO2 and CO in the absence of H-2 cofeed. When CO2 was preadsorbed followed by H-2 flow, methane was produced, as well as traces of C-3-C-4 hydrocarbons, but no evidence of the reverse water gas shift reaction was found. Use was made of carbon-14-labeled carbon dioxide to track CO2 conversion and selectivity during reaction of syngas mixtures with different ratios of CO, CO2, and H-2. Absence of C-14 in unconverted CO and the unequal molar concentration of C-14 in the products from reaction at 220 degrees C and 2 MPa provided strong evidence that (CO2)-C-14 was not converted by the reverse water gas shift reaction. The antecedence of the carbon from CO2 mattered, and the carbon did not become part of a common carbon pool for hydrocarbon synthesis. Conversion of CO2 proceeded by a pathway separate from CO. Conclusions drawn from this experimental study were employed to determine implications for the industrial application of Co-catalyzed Fischer-Tropsch synthesis.
引用
收藏
页码:1189 / 1196
页数:8
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