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Comparison between zeolite [beta] and [gamma]-Al[sub 2]O[sub 3] supported Pt for reforming reactions

Journal Article · · Journal of Catalysis; (United States)
;  [1]
  1. State Univ. of New York, Buffalo (United States)
The performance of zeolite [beta] supported platinum as a bifunctional catalyst for the reforming of n-hexane, methylcyclopentane, and cyclohexane, typical representatives of reforming feeds, has been examined under low severity conditions. A comparison under the same conditions with [gamma]-Al[sub 2]O[sub 3] supported Pt was carried out. Both catalysts were impregnated with 0.5 wt % Pt. It is found that [beta]-zeolite exhibits skeletal isomerization reactions to a higher extent than alumina, producing molecules with much higher octane number than the feed molecules. Bimolecular alkylation reactions that take place in the zeolite pores have as a result the formation of products with a carbon number larger than that of the feed molecule. The enlargement of the cyclic ring of methylcyclopentane leads at suitable temperatures to aromatics, a reaction of great importance for reforming. This behavior is a result of the relatively large acidity of the zeolite and of its pore structure that favors the proximity among different molecules increasing the probability for reaction. In contrast, Pt/Al[sub 2]O[sub 3] stimulates dehydrogenation-hydrogenation and to a smaller extent skeletal isomerization. This [beta]-zeolite is deactivated more easily than alumina due to the coke build up on the acidic sites. The characterization of the catalysts has been carried out using XRD, NH[sub 3]-TPD, SEM, FTIR, BET, TEM, and H[sub 2]-chemisorption. 50 refs., 9 figs., 7 tabs.
OSTI ID:
6374902
Journal Information:
Journal of Catalysis; (United States), Journal Name: Journal of Catalysis; (United States) Vol. 140:2; ISSN 0021-9517; ISSN JCTLA5
Country of Publication:
United States
Language:
English

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