Synthesis and Characterization of Silica-Supported Cobalt Phosphide Catalysts for CO Hydrogenation

被引:31
|
作者
Song, Xiangen [1 ,3 ]
Ding, Yunjie [1 ,2 ]
Chen, Weimiao [1 ]
Dong, Wenda [1 ,3 ]
Pei, Yanpeng [1 ,3 ]
Zang, Juan [1 ,3 ]
Yan, Li [1 ]
Lu, Yuan [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Dalian Inst Chem Phys, State Key Lab Catalysis, Dalian 116023, Peoples R China
[3] Chinese Acad Sci, Grad Sch, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
TRANSITION-METAL PHOSPHIDES; SYNTHESIS GAS CONVERSION; HIGHER-ALCOHOL SYNTHESIS; HYDRODESULFURIZATION PROPERTIES; RH CATALYSTS; SYNGAS; PROMOTER; ETHANOL; LA2O3;
D O I
10.1021/ef301391f
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
A series of silica supported cobalt phosphides with different metal/P molar ratios were synthesized by means of a temperature programmed reduction (TPR) method. Their catalytic performances of CO hydrogenation were tested in a fixed-bed reactor under conditions of 553 K, 5.0 MPa, and H-2/CO = 2 (molar). The catalytic activity of the phosphides ranked in the following order: Co2P/SiO2 < Co4P/SiO2 < Co8P/SiO2 (x denotes the molar ratio of metal to P). It is interesting to find that C-2(+) oxygenates were the main product over the CoxP catalysts. Evidence from X-ray photoelectron spectroscopy (XPS) and high-resolution transmission electron microscopy (HRTEM) measurements proved that the Co delta+ species might be the active sites for the formation of higher oxygenates during CO hydrogenation.
引用
收藏
页码:6559 / 6566
页数:8
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