Skip to main content
Log in

Kinetics of heptane reforming on Pt/L zeolite

  • Published:
Catalysis Letters Aims and scope Submit manuscript

Abstract

The kinetics of heptane reforming over 0.64% Pt/KBaL have been measured over a wide range of conditions from 390 to 475 ° C, 0.05 to 1.00 atm heptane, and 0.2 to 25.0 atm hydrogen. Below about 6 atm H2, the catalyst deactivates due to carbon fouling of the platinum particles. The reaction rate increases with hydrogen pressure under these conditions, presumably because this accelerates the rate of carbon hydrogenation off the metal surface. Above 6 atm H2, no deactivation occurs. The activation energies and reaction orders in heptane and hydrogen at high H2 pressure are: 39 kcal/mol, 0.7 and −1.9 for hydrogenolysis; 60 kcal/mol, 0.6 and −2.8 for isomerization; and 58 kcal/mol, 0.4 and −2.7 for dehydrocyclization. These kinetics are the same as those observed over platinum on nonacidic supports, and indicate that the reaction mechanism on Pt/KBaL is no different from that on monofunctional Pt catalysts.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. J.R. Bernard, in:Proc. 5th Int. Congr. on Zeolites, ed. L.V.C. Rees (Heyden, London, 1980) p. 686.

    Google Scholar 

  2. T.K. Hughes, W.C. Buss, P.W. Tamm and R.L. Jacobson, Stud. Surf. Sci. Catal. 28 (1986) 725.

    Google Scholar 

  3. P.W. Tamm, D.H. Mohr and C.R. Wilson, Stud. Surf. Sci. Catal. 38 (1988) 335.

    Google Scholar 

  4. C. Besoukhanova, J. Guidot, D. Barthomeuf, M. Breysse and J.R. Bernard, J. Chem. Soc. Faraday Trans. 77 (1981) 1595.

    Google Scholar 

  5. E.G. Derouane and D.J. Vanderveken, Appl. Catal. 45 (1988) L15.

    Google Scholar 

  6. G. Larsen and G.L. Haller, Catal. Lett. 3 (1989) 103.

    Google Scholar 

  7. B.J. McHugh, G. Larsen and G.L. Haller, J. Phys. Chem. 94 (1990) 8621.

    Google Scholar 

  8. S.J. Tauster and J.J. Steger, J. Catal. 125 (1990) 387.

    Google Scholar 

  9. G.S. Lane, F.S. Modica and J.T. Miller, J. Catal. 129 (1991) 145.

    Google Scholar 

  10. R.J. Davis and E.G. Derouane, J. Catal. 132 (1991) 269.

    Google Scholar 

  11. D.J. Ostgard, L.M. Kustov, K.R. Poeppelmeier and W.M.H. Sachtler, J. Catal. 133 (1992) 342.

    Google Scholar 

  12. E. Mielczarski, S.B. Hong, R.J. Davis and M.E. Davis, J. Catal. 134 (1992) 359.

    Google Scholar 

  13. E. Iglesia and J.E. Baumgartner, in:Proc. 10th Int. Congres on Catalalysis, Budapest, 19–25 July 1992, to be published.

  14. J.H. Sinfelt, in:Catalysis, Science and Technology, Vol. 1, eds. J.R. Anderson and M. Boudart (Springer, Berlin, 1981) ch. 5, p. 257.

    Google Scholar 

  15. W.J. Han, A.B. Kooh and R.F. Hicks, Catal. Lett. 18 (1993) 193.

    Google Scholar 

  16. P.A. Newell and L.V.C. Rees, Zeolites 3 (1983) 22, 28.

    Google Scholar 

  17. J.C. Rohrer, H. Hurwitz and J.H. Sinfelt, J. Phys. Chem. 65 (1961) 1458.

    Google Scholar 

  18. M.A. Pacheco and E.E. Petersen, J. Catal. 86 (1984) 75.

    Google Scholar 

  19. E. Kikuchi, M. Tsurumi and Y. Morita, J. Catal. 22 (1971) 226.

    Google Scholar 

  20. F.G. Gault, Adv. Catal. 30 (1981) 1.

    Google Scholar 

  21. J.H. Sinfelt, H. Hurwitz and J.C. Rohrer, J. Phys. Chem. 64 (1960) 892.

    Google Scholar 

  22. M. Guisnet, V. Fouche, M. Belloum, J.P. Bournonville and C. Travers, Appl. Catal. 71 (1991) 295.

    Google Scholar 

  23. S.A. Goddard, M.D. Amiridis, J.E. Rekoske, N. Cardona-Martinez and J.A. Dumesic, J. Catal. 117 (1989) 155.

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kooh, A.B., Han, WJ. & Hicks, R.F. Kinetics of heptane reforming on Pt/L zeolite. Catal Lett 18, 209–218 (1993). https://doi.org/10.1007/BF00769439

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00769439

Keywords

Navigation