Iron catalysts supported on carbon nanotubes for Fischer-Tropsch synthesis: Effect of catalytic site position

被引:167
作者
Abbaslou, Reza M. Malek [1 ]
Tavassoli, Ahmad [2 ]
Soltan, Jafar [1 ]
Dalai, Ajay K. [1 ]
机构
[1] Univ Saskatchewan, Dept Chem Engn, Saskatoon, SK S7N 5A9, Canada
[2] Univ Tehran, Univ Coll Sci, Sch Chem, Tehran, Iran
关键词
Fischer-Tropsch synthesis; Iron; Carbon nanotubes; Site position; CO HYDROGENATION; COBALT;
D O I
10.1016/j.apcata.2009.07.025
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
In order to study the effects of catalytic site position on Fischer-Tropsch (FT) reactions, a method was developed to control the position of the catalytic sites on either inner or outer surface of carbon nanotubes (CNTs). TEM analyses revealed that more than 70-80% of iron oxide particles can be controlled to be positioned at inner or outer surface of the nanotubes. Based on H-2-TPR analysis, deposition of iron oxide inside the nanotube pores resulted in easier reduction of the oxide at a lower temperature (from 418 to 381 degrees C). Catalytic performances of the catalysts in terms of FT experiment were tested in a fixed-bed reactor. According to the results of FT experiments, both catalysts showed similar initial %CO conversion (similar to 90%). However, the catalyst with catalytic sites inside the pores exhibited higher selectivity to heavier hydrocarbons. In addition, deposition of catalytic sites on interior surface of the nanotubes resulted in a more stable catalyst, while its counterpart experienced deactivation within a period of 125 h due to catalytic sites sintering. It is concluded that encapsulation of catalytic sites inside the nanotubes prevents the catalytic site agglomeration. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:47 / 52
页数:6
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