Fischer–Tropsch synthesis over γ-alumina-supported cobalt catalysts: Effect of support variables
A systematic study of the effect of γ-Al 2O 3 support variables on Fischer–Tropsch synthesis activity and selectivity was carried out at industrially relevant conditions ( T = 483 K , P = 20 bar , H 2 / CO = 2.1 ). A total of 13 catalysts were prepared by incipient wetness impregnation of γ-Al 2...
Saved in:
Published in | Journal of catalysis Vol. 248; no. 1; pp. 89 - 100 |
---|---|
Main Authors | , , , , , , |
Format | Journal Article |
Language | English |
Published |
Amsterdam
Elsevier Inc
15.05.2007
Elsevier |
Subjects | |
Online Access | Get full text |
Cover
Loading…
Summary: | A systematic study of the effect of
γ-Al
2O
3 support variables on Fischer–Tropsch synthesis activity and selectivity was carried out at industrially relevant conditions (
T
=
483
K
,
P
=
20
bar
,
H
2
/
CO
=
2.1
). A total of 13 catalysts were prepared by incipient wetness impregnation of
γ-Al
2O
3 supports of varying pore characteristics and chemical purities with aqueous solutions containing the required amounts of cobalt and rhenium precursor to give nominal loadings of 20 and 0.5 wt%, respectively. The catalysts were analysed for cobalt, rhenium, nitrogen, and sodium and characterised by nitrogen adsorption/desorption, mercury intrusion, X-ray diffraction, hydrogen chemisorption, temperature-programmed reduction, and oxygen titration. The size of the Co
3O
4 cobalt particles was controlled by the support pore size, with small particles formed in narrow pores and large particles formed in wide pores. The degree of reduction increased with increasing catalyst pore size and Co
3O
4 particle size. The catalysts contained different amounts of sodium (20–113 ppm) and the site-time yield decreased with increasing sodium content. Positive correlations were found between cobalt particle size and C
5+ selectivity and between catalyst pore size and C
5+ selectivity. The results indicate that the C
5+ selectivity is controlled by the size and appearance of cobalt particles. |
---|---|
ISSN: | 0021-9517 1090-2694 |
DOI: | 10.1016/j.jcat.2007.03.008 |