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Carbon-14 tracer study of the conversion of labeled n-propylcyclopentane during n-octane aromatization with a Pt-zeolite L catalyst

Journal Article · · Journal of Catalysis; (United States)
; ; ;  [1]
  1. Univ. of Kentucky, Lexington (United States)
n-Propylene cyclopentane or n-propylcyclopentane labeled in the ring with {sup 14}C was converted together with n-octane using a Pt-KL zeolite catalyst operating at 482 C and ca. 14 bar. The products indicate that hydrogenolysis to produce isooctanes, not ring expansion to produce aromatics, is the major reaction pathway for the alkyl cyclopentane compound. Dilution of the {sup 14}C activity in n-propylcyclopentane during the conversion shows that C{sub 5} as well as C{sub 6} cyclization occurs during the conversion of n-octane. The current data were obtained with a catalyst that has a Pt crystal size range that is similar to those reported earlier. Furthermore, the conversion data for n-octane and n-propylcyclopentane using the Pt-KL zeolite catalyst are very similar to data obtained with catalysts based on other nonacidic supports where the Pt crystals cannot be located in a zeolite type channel. Thus, for n-octane conversion, it appears that the Pt in L zeolite catalysts has selectivities that are similar to Pt on other nonacidic supports.
OSTI ID:
6984572
Journal Information:
Journal of Catalysis; (United States), Journal Name: Journal of Catalysis; (United States) Vol. 134:1; ISSN 0021-9517; ISSN JCTLA
Country of Publication:
United States
Language:
English