Textural Structure of Co-based Catalysts and their Performance for Fischer-Tropsch Synthesis

被引:5
|
作者
Wang, Jungang [1 ,2 ]
Li, Debao [1 ]
Hou, Bo [1 ]
Jia, Litao [1 ]
Chen, Jiangang [1 ]
Sun, Yuhan [1 ,3 ]
机构
[1] Chinese Acad Sci, State Key Lab Coal Convers, Inst Coal Chem, Taiyuan 030001, Shanxi, Peoples R China
[2] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Low Carbon Convers Ctr, Shanghai Adv Res Inst, Shanghai 201203, Peoples R China
关键词
Cobalt catalyst; Pore size distribution; Fischer-Tropsch synthesis; PORE-SIZE; COBALT CATALYSTS; SILICA; GAMMA-AL2O3; SUPPORTS; CO/SIO2; ALUMINA; RAMAN;
D O I
10.1007/s10562-010-0449-2
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
Both mono- and bi-modal Co-based Fischer-Tropsch Synthesis (FTS) catalysts were prepared by incipient-wetness impregnation (IWI). XRD and N-2 physisorption revealed that the catalyst with a bi-modal distribution of 2.5-17 nm had the smallest size of cobalt crystal. In this case, the Raman absorbance shifted toward lower frequencies due to the size quantization effect. Furthermore, H-2-TPR indicated a lower reducibility originated from the interaction between small crystalline cobalt and silica. Such bi-modal structure catalysts showed a better FTS performance, and particularly the bi-modal mesopores catalyst presented the lowest methane selectivity, the highest activity and the highest selectivity to C-5-C-18 hydrocarbons, which might be due to the confinement of mesopore to the cobalt particles.
引用
收藏
页码:127 / 133
页数:7
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