Carbon monoxide hydrogenation on cobalt/zeolite catalysts

被引:21
|
作者
Wang, WJ
Lin, HY
Chen, YW [1 ]
机构
[1] Natl Cent Univ, Dept Chem Engn, Nanocatalysis Res Ctr, Chungli 320, Taiwan
[2] Far E Coll, Dept Chem Engn, Tainan 744, Taiwan
关键词
Fischer-Tropsch synthesis; carbon monoxide hydrogenation; cobalt; zeolite;
D O I
10.1007/s10934-005-5227-y
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The synthesis of hydrocarbons from catalytic hydrogenation of CO/H-2 was investigated over Co/zeolite catalysts at 1 atm, 493-553 K, H-2/CO = 2, and GHSV = 1200. Various zeolites, such as NaA, NaX, NaY, KL and NaMordenite, were used as the supports. The catalysts were prepared by impregnation and were characterized by H-2/CO chemisorption and temperature-programmed reduction (TPR). Based on TPD measurements, the CO/H2 adsorption ratio can be used as an index for the extent of metal-zeolite interaction. The stronger the metal-zeolite interaction is, the higher the Co/H-2 adsorption ratio on metal is. The activity and selectivity of cobalt supported in zeolites were affected by complex factors such as framework structure, Si/Al ratio, and the complementary cations. The activity of the catalyst is in the order: Co/KL > Co/NaX > Co/NaY > Co/NaMordenite > Co/NaA. All of the Co/zeolite catalysts had a very high selectivity to C-2-C-4 olefins, which would decrease with increasing reaction temperature. Cobalt oxide supported in zeolite was difficult to reduce. Increasing the reduction temperature could increase the reducibility of cobalt and resulted in the increase of activity.
引用
收藏
页码:5 / 12
页数:8
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