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By Harrison G. R.

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CT11. 9. References. 1. Cedigaz, July 1996. 2. Clerici, G. and Zennaro, R. (1997) Recent trends of research in natural gas utilization, La Chimica e L 'Industria, February, 47-54. 31 3. International Energy Agency. Report on Natural Gas Transportation (1994) OECD Paris, Pag 3. 4. Parkyns, N. , Warburton, C. I. and Wilson, J. D. , Catalysis Today, 18, 385-442. 5. Axeldord, M. , Gaffney A. , Pitchai R. and Sofranko J. A. E. , pp. 93-101 6. , Zawodzinski, T. and Gottesfeld, S. (1996) Pem Fuel Cells for Transportation and Stationary Power Generation Applications, in T.

21. H. ( 1991) The catalytic conversion of methane to higher hydrocarbons, Studies in Surface Science and Catalysis, 61, 3. 22. H. (1994) New Directions For the Catalytic Conversion of Methane. Final Report, November 1987-0ctober 1993. Report 94 N° GRJ94/0375; Order N° PB95-I54I83, NTIS. 23. X. and Lunsford, J. (1985) Formation of Gas-Phase Methyl Radicals Over MgO, J Am. Chern. , 107, 58. 24. Ito, T. H. (1985) Synthesis of ethylene and ethane by partial oxidation of methane over lithium-doped magnesium oxide, Nature, 314, 721.

Reaction scheme for propane aromatization on Ga/ZSM-5 catalysts. Although the reaction sequence is frequently rationalized on the basis of a classical bifunctional mechanism, with the participation of both acidic and metallic sites, the nature and location of the metal cations and their catalytic role during propane aromatization is still being questioned [13, 14]. It is recognized that both the metallic and acidic sites need to be in close proximity for achieving high aromatization selectivity.

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