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Novel precipitated iron Fischer–Tropsch catalysts with Fe3O4 coexisting with α-Fe2O3.

Authors :
Baoshan Wu
Lei Tian
Hongwei Xiang
ZhixinZhang
Yong-Wang Li
Source :
Catalysis Letters; Jun2005, Vol. 102 Issue 3/4, p211-218, 8p
Publication Year :
2005

Abstract

The present study was undertaken to investigate the catalytic behavior of an industrial iron catalyst (Fe/Cu/K/SiO<subscript>2</subscript>) prepared from ferrous sulfate precursor for Fischer–Tropsch (FT) synthesis, in which different amount of Fe<subscript>3</subscript>O<subscript>4</subscript> coexist with α-Fe<subscript>2</subscript>O<subscript>3</subscript>. The catalyst samples were characterized by BET, XRD, H<subscript>2</subscript>-TPR and Mössbauer effect spectroscopy (MES). The FT synthesis performance of the catalysts were carried out in a fixed bed reactor (FBR) under reaction conditions of 250 °C, 1.5 MPa, 2.0 nL/g-cat/h, and H<subscript>2</subscript>/CO=2/1 for 200 h. The results from XRD and MES for the catalyst samples of pre- and post-reduction indicate that more iron carbides form in the catalysts that have lower Fe<subscript>3</subscript>O<subscript>4</subscript> contents. H<subscript>2</subscript>-TPR for the catalysts displays that Fe<subscript>3</subscript>O<subscript>4</subscript> may facilitate the reduction of catalysts only when it was highly dispersed. FT reaction study in the FBR shows that the catalysts become more active with the decrease of Fe<subscript>3</subscript>O<subscript>4</subscript> contents in the catalysts. However, the catalyst with certain amount of highly dispersed Fe<subscript>3</subscript>O<subscript>4</subscript> exhibited high FT synthesis activity with CO conversion more than 75%. The catalyst also displayed much less olefins selectivity. A comparison of FTS performances of one of these catalysts with some known catalysts was also made in this paper. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1011372X
Volume :
102
Issue :
3/4
Database :
Complementary Index
Journal :
Catalysis Letters
Publication Type :
Academic Journal
Accession number :
17608705
Full Text :
https://doi.org/10.1007/s10562-005-5858-2