Fischer-Tropsch synthesis over Pt/Co/Al2O3 catalyst: Improvement in catalyst stability by activation with diluted CO

被引:5
|
作者
Jalama, Kalala [1 ]
Ma, Wenping [2 ]
Jacobs, Gary [2 ,3 ]
Sparks, Dennis [2 ]
Qian, Dali [4 ]
Davis, Burtron H. [2 ]
机构
[1] Univ Johannesburg, Dept Chem Engn, POB 17011, ZA-2028 Johannesburg, South Africa
[2] Univ Kentucky, Ctr Appl Energy Res, 2540 Res Pk Dr, Lexington, KY 40511 USA
[3] Univ Texas San Antonio, Dept Biomed & Chem Engn, Dept Mech Engn, One UTSA Circle, San Antonio, TX 78249 USA
[4] Univ Kentucky, Electron Microscopy Ctr, 145 Graham Ave, Lexington, KY 40506 USA
关键词
CO activation; Cobalt; Fischer-Tropsch; Stability; CARBON-MONOXIDE HYDROGENATION; SUPPORTED COBALT CATALYSTS; DEACTIVATION; NANOPARTICLES; CARBIDE; ETHANOL; IMPACT; H-2;
D O I
10.1016/j.apcata.2020.117645
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Fischer-Tropsch cobalt-based catalyst deactivation is one of the major challenges facing gas-to-liquids processes. Changes in catalyst formulation and pre-treatment methods are among the promising routes to address this challenge. In this study, diluted CO was used to pre-treat a 0.5%Pt/25%Co/Al2O3 catalyst, in comparison to H-2, and the resulting effects on catalyst stability, activity and product selectivity were evaluated. The investigation was performed using BET, TEM, TPR, XPS and XRD techniques, combined with catalyst evaluation in a 1 L continuously stirred tank reactor. The results reveal that microporous carbon shells encapsulate Co particles during activation by CO at higher temperatures, resulting in lower activity and higher methane selectivity compared to the H-2-reduced catalyst, at early reaction times. However, the CO-activated catalyst displayed superior stability, resulting in better performance at extended time-on-stream compared to a deactivating H-2-activated catalyst, which showed an increase in CH4 selectivity and a decline in C5+ hydrocarbon formation rate.
引用
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页数:11
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