Hostname: page-component-586b7cd67f-rdxmf Total loading time: 0 Render date: 2024-11-24T11:35:23.622Z Has data issue: false hasContentIssue false

Hybrid Catalysts: Internal or External Configuration for Better Catalytic Performance?

Published online by Cambridge University Press:  10 February 2011

R. Le Van Mao
Affiliation:
Department of Chemistry and Biochemistry, Concordia University, 1455 De Maisonneuve West, Montreal, Quebec, H3G 1M8 Canada
M. A. Saberi
Affiliation:
Department of Chemistry and Biochemistry, Concordia University, 1455 De Maisonneuve West, Montreal, Quebec, H3G 1M8 Canada
J. A. Lavigne
Affiliation:
Department of Chemistry and Biochemistry, Concordia University, 1455 De Maisonneuve West, Montreal, Quebec, H3G 1M8 Canada
S. Xiao
Affiliation:
Department of Chemistry and Biochemistry, Concordia University, 1455 De Maisonneuve West, Montreal, Quebec, H3G 1M8 Canada
G. Denes
Affiliation:
Department of Chemistry and Biochemistry, Concordia University, 1455 De Maisonneuve West, Montreal, Quebec, H3G 1M8 Canada
Get access

Abstract

Hybrid catalysts with the external configuration for the cocatalyst showed enhanced product diffusion rates in the n-octane hydrocracking, only if the reaction was carried out at relatively high temperatures. In the n-heptane isomerization, direct incorporation of the Al species into the HY zeolite micropores produced sorption sites which positively affected the selectivity to liquid isomers. Such as internal hybrid configuration resulted in a more important increase in the liquid isomer selectivity than that given by the external hybrid configuration, both systems being designed for better product outward-diffusion.

Type
Research Article
Copyright
Copyright © Materials Research Society 1998

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

REFERENCES

1. Le Van Mao, R., Zeolites, submitted.Google Scholar
2. Yao, J. and Le Van Mao, R., Catal. Lett. 11, 191 (1991).Google Scholar
3. Le Van Mao, R., Yao, J., Dufresne, L., Carli, R., Catal. Today 31, 247 (1996).Google Scholar
4. Xiao, S. and Le Van Mao, R., Microporous Mater. 4, 435(1995).Google Scholar
5. Le Van Mao, R., U.S. Patent 4,732,881 (Mar. 22, 1988).Google Scholar
6. Derouane, E.G., Andre, J.M. and Lucas, A.A., J. Catal. 110, 58 (1988).Google Scholar
7. Barrer, R.M., J. Chem. Soc., Faraday Trans. 86 (7), 1123 (1990).Google Scholar
8. Xiao, S., Le Van Mao, R. and Denes, G., J. Mater. Chem. 5 (6), 1251 (1995).10.1039/jm9950501251Google Scholar
9. Miller, S.J., Microporous Mater., 2, 439 (1994).Google Scholar
10. Taylor, R.J. and Petty, R.H., Applied Catal. A, 119, 121 (1994).Google Scholar
11. Parlitz, B., Schreier, E., Zubowa, H.L., Eckelt, R., Lieske, E., Lischke, G. and Fricke, R., J. Catal. 155, 1 (1995).Google Scholar