Carbon-encapsulated metallic Co nanoparticles for Fischer-Tropsch to olefins with low CO2 selectivity

被引:18
作者
Gong, Kun [1 ,2 ]
Wei, Yao [2 ,4 ,5 ]
Dai, Yuanyuan [6 ]
Lin, Tiejun [1 ]
Yu, Fei [1 ]
An, Yunlei [1 ]
Wang, Xinxing [1 ]
Sun, Fanfei [5 ]
Jiang, Zheng [4 ,5 ]
Zhong, Liangshu [1 ,3 ]
机构
[1] Chinese Acad Sci, Shanghai Adv Res Inst, CAS Key Lab Low Carbon Convers Sci & Engn, Shanghai 201210, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100049, Peoples R China
[3] ShanghaiTech Univ, Sch Phys Sci & Technol, Shanghai 201210, Peoples R China
[4] Chinese Acad Sci, Shanghai Inst Appl Phys, Shanghai 201800, Peoples R China
[5] Chinese Acad Sci, Shanghai Adv Res Inst, Shanghai Synchrotron Radiat Facil, Shanghai 201204, Peoples R China
[6] China Erdos Elect Power & Met Grp Co Ltd, Ordos 016064, Inner Mongolia, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENT AND ENERGY | 2022年 / 316卷
基金
上海市自然科学基金;
关键词
Fischer-Tropsch to olefins; Syngas conversion; Core-shell catalysts; Metallic cobalt; Low CO2 selectivity; LIGHT OLEFINS; CATALYSTS; SYNGAS; CONVERSION; MECHANISM; NANOPRISMS; ALCOHOLS; PROMOTER; INSIGHT; DESIGN;
D O I
10.1016/j.apcatb.2022.121700
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
Tuning Fischer-Tropsch synthesis products of metallic Co-based catalysts from paraffins to value-added olefins chemicals attracts great attention but remains challenging. Herein, we succeed in designing the carbon layers confined cobalt metal core-shell nanocatalyst (Co@C) via a reduction-carburization-pyrolysis (RCP) pretreatment of Co/SiO2, which exhibits highly efficient for Fischer-Tropsch to olefins (FTO) with negligible Water-GasShift activity. At 250 degrees C and 5 bar, 56.4 % of olefins selectivity and limited CO2 selectivity (5.8 %) are achieved for Mn-promoted Co@C nanocatalyst with at least 200 h of stability running. The electronic effect of carbon layers and Mn promoter as well as the confinement structure tailor the local chemical environment and weaken the hydrogenation ability of Co metal sites, thus improving the selectivity toward olefins while largely reducing the formation of CH4 and CO2. This work develops an effective strategy for the rational design of highly active and stable metallic Co-based FTO catalysts with high carbon efficiency.
引用
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页数:12
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