Effect of CO conversion upon product distribution using bimetallic Co-Ni mesoporous silica catalyst for Fischer-Tropsch synthesis: a comparative study of fixed-bed reactor and slurry continuous stirred tank reactor

被引:3
作者
Sun, Yong [1 ]
Yang, Gang [2 ]
Sun, Zhi [3 ]
Zhang, Lian [4 ]
机构
[1] Edith Cowan Univ, Sch Engn, 270 Joondalup Dr, Joondalup, WA 6027, Australia
[2] Anpeng Energy Grp, Beijing 100190, Peoples R China
[3] Chinese Acad Sci, Inst Proc Engn, Natl Engn Lab Hydrometallurg Cleaner Prod Technol, Beijing 100190, Peoples R China
[4] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
关键词
Fischer-Tropsch synthesis; fixed-bed reactor; slurry continuous stirred tank reactor; comparative study; ACTIVATED CARBON; MEMBRANE REACTOR; HEAT-TRANSFER; CHAIN-LENGTH; IRON; OPTIMIZATION; PERFORMANCE; WATER; REMOVAL; CORNCOB;
D O I
10.1002/apj.2094
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
Fischer-Tropsch synthesis was studied on mesoporous silica supported bimetallic Co-Ni catalyst in the fixed-bed reactor (FBR) and slurry continuous stirred tank reactor (CSTR) under different CO conversions by fixing other process parameters, for example, reaction temperature (300 degrees C), syngas ratio (2), and total pressure (3 MPa). The CO conversion is more sensitive in responding to the decrease of gas hour space velocity in FBR than that in CSTR. The intra-particle diffusional limitation was much improved in the CSTR system during Fischer-Tropsch synthesis due to the smaller particle size of the catalyst. The selectivity of gasoline fraction (C-5-C-13) was larger in CSTR than that in FBR when it was operated at relatively higher CO conversions (65%). The FBR tends to produce higher selectivity of longer-chain hydrocarbons than that in CSTR when the CO conversion was kept at around 22%. The increased 1-olefin selectivity was observed in both FBR and CSTR as CO conversion decrease with the FBR being more sensitive in responding to the CO conversion variation. The CSTR is found to be more effective in increasing light olefin fraction (C-2-C-6) when the CO conversion varies from 22 to 65%. (C) 2017 Curtin University of Technology and John Wiley & Sons, Ltd.
引用
收藏
页码:518 / 526
页数:9
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