Surface speciation of Co based Fischer-Tropsch catalyst under reaction conditions: Deactivation by coke or by oxidation?

被引:11
|
作者
Kocic, Stefan [1 ]
Valero, Manuel Corral [1 ]
Schweitzer, Jean-Marc [1 ]
Raybaud, Pascal [1 ]
机构
[1] IFP Energies Nouvelles, Rond Point Echangeur Solaize, BP 3, F-69360 Solaize, France
关键词
Fischer-Tropsch; Deactivation; Coke precursors; Oxidation; Cobalt; DENSITY-FUNCTIONAL THEORY; SUPPORTED COBALT FISCHER; TOTAL-ENERGY CALCULATIONS; FIXED-BED REACTOR; CARBON-MONOXIDE; REALISTIC CONDITIONS; HYDROGEN ADSORPTION; HIGH COVERAGES; WATER-VAPOR; MECHANISM;
D O I
10.1016/j.apcata.2019.117332
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
Loss of catalyst activity and selectivity with time-on-stream are one of the greatest limitations for the industrial use of Cobalt based Fischer-Tropsch (FT) catalysis. Despite much work on this area, there is still a lack of consensus about the causes leading to catalyst deactivation. Some of the most common hypotheses are oxidation and carbonization of the active phase. In our work we present the free energy of C alpha H beta O gamma surface deposition on Co (111) for a wide range of surface coverages under FT reaction conditions. These results present a comprehensive study in which the trends for hydrocarbon-species deposition, cobalt oxidation, and hydrocarbon-induced surface reconstruction are thoroughly compared. The formation of unavoidable branched species leads to deactivation by coke; O may be present in surface intermediates but direct Co-O interaction is unlikely at these conditions.
引用
收藏
页数:12
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