Highly productive and robust core@shell HeatPath SiC-Al2O3 @Co/Re/Al2O3 catalyst for Fischer-Tropsch synthesis

被引:2
作者
Zhang, Rui [1 ]
Li, Junrui [1 ,5 ]
Tonkovich, Anna Lee [2 ]
Lockhart, Cody [3 ]
Wang, Xiaoyan [3 ]
Hu, Wenda [1 ]
Karroum, Hafsa [1 ]
Seabaugh, Matthew [3 ]
Kruse, Norbert [1 ,4 ]
Wang, Yong [1 ,4 ]
机构
[1] Washington State Univ, Voiland Sch Chem Engn & Bioengn, Pullman, WA 99164 USA
[2] Tonkomo LLC, Gilbert, AZ 85297 USA
[3] Nexceris LLC, Lewis Ctr, OH USA
[4] Pacific Northwest Natl Lab, Inst Integrated Catalysis, Richland, WA 99332 USA
[5] Clark Atlanta Univ, Dept Chem, Atlanta, GA 30314 USA
关键词
Fischer-Tropsch synthesis; Core@shell structure; Cobalt catalyst; Temperature control; C5+ hydrocarbon; Methane selectivity; COBALT CATALYST; REACTORS; PERFORMANCE; PRECURSOR;
D O I
10.1016/j.apcata.2023.119419
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
Co-based catalysts are highly active for synthesizing long-chain paraffins through Fischer-Tropsch synthesis. However, their exothermic reactions can cause overheating and catalyst deactivation. To address this, thermally conductive SiC-Al2O3 pellets (HeatPath (TM)) were coated with a Co/Re/Al2O3 shell, significantly boosting the CO conversion rate and the yield of C-2 4 and C5+ hydrocarbons over a wide range of temperatures by dissipating the reaction heat. The core@shell HeatPath@Co/Re/Al2O3 catalyst demonstrated high productivity (up to 19.7 g(CO) g(cat)(-1) h(-1)), exceptional long-term stability over 660 h time-on-stream, with high-temperature operation up to 260 degrees C, a low CH4 selectivity (7.1 %) and a chain growth probability (alpha) > 0.8. In contrast, the irreversible deactivation of a powder Co/Re/Al2O3 catalyst started at 195 degrees C, resulting in >60 % CH4 selectivity and similar to 100 % CO conversion due to excessive local heat. The CO conversion rate on the core@shell catalyst could be further improved by increasing the H-2/CO ratio and temperature, with commercially viable CH4 selectivity.
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页数:7
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