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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.
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页码:47 / 52
页数:6
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