Fischer-Tropsch synthesis over cobalt catalysts supported on nanostructured alumina with various morphologies

被引:29
|
作者
Liu, Chengchao [1 ]
Li, Jinlin [1 ]
Zhang, Yuhua [1 ,2 ]
Chen, Sufang [2 ,3 ]
Zhu, Junjiang [1 ]
Liew, Kongyong [1 ]
机构
[1] S Cent Univ Nationalities, Key Lab Catalysis & Mat Sci, State Ethn Affairs & Commiss, Minist Educ, Wuhan 430074, Hubei, Peoples R China
[2] Soochow Univ, Coll Chem Chem Engn & Mat Sci, Suzhou 215123, Peoples R China
[3] Wuhan Inst Technol, Sch Chem Engn & Pharm, Key Lab Green Chem Proc, Minist Educ, Wuhan 430073, Hubei, Peoples R China
基金
美国国家科学基金会;
关键词
Fischer-Tropsch synthesis; Cobalt catalysts; Nanostructured alumina; Morphology; PORE-SIZE; DEACTIVATION; SELECTIVITY; PERFORMANCE; GAMMA-AL2O3;
D O I
10.1016/j.molcata.2012.07.009
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
Nanostructured aluminas with controllable morphologies were prepared and used as support of cobalt catalysts for Fischer-Tropsch synthesis. The supported cobalt catalysts were prepared by incipient wetness impregnation method and characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), temperature programmed reduction (TPR), N-2 adsorption-desorption, hydrogen chemisorption and oxygen titration. Catalytic activity of the cobalt catalysts for Fischer-Tropsch synthesis (FTS) was evaluated on a fixed bed reactor. It was found that the nanostructured alumina supports undergo reconstruction during the catalyst preparation resulting in catalysts having high dispersion after reduction. The cobalt catalyst supported on the nanostructured alumina increased the CO conversion by 20-30%, compared to commercial alumina. Among the nanostructured catalysts, the alumina nanorods supported catalyst, shows the best dispersion and highest CO initial conversion. Our work disclosed that the alumina nanofibers supported catalysts have larger, stable and interconnected bird nest-like pores. In addition, the structure exhibited higher stability and lower methane selectivity for FTS. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:335 / 342
页数:8
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