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Hydrocracking polycyclic hydrocarbons over a dual-functional zeolite (faujasite)-based catalyst

Journal Article · · Ind. Eng. Chem. Process Des. Dev.; (United States)
DOI:https://doi.org/10.1021/i200022a011· OSTI ID:5613993

Mixtures of two-, three-, and four-ring (naphthalene, phenanthrene, and pyrene) structures were hydrocracked over a nickel-tungsten sulfide ultrastable zeolite Y catalyst. The hydrocracking of tetralin and phenanthrene proceeds by elimination of butanes to form C/sub 6/ and C/sub 10/ hydrocarbons primarily. Isomerization of saturated six-member rings to methyl-substituted five-member rings is also prominent. The presence of 1-cyclohexyl-2-phenylethane in the products from phenanthrene hydrocracking suggests an alternative reaction path for the hydrocracking of structures containing adjacent saturated rings. Pyrene hydrocracking proceeds primarily by elimination of propane followed by butanes elimination, i.e., C/sub 16/ ..-->.. C/sub 13/ ..-->.. C/sub 10/ ..-->.. C/sub 6/. The C/sub 13/ intermediates are mostly hydrogenated phenalenes. The zeolite-based catalyst was very active in hydrocracking pyrene (critical diameter = 9 A) and smaller molecules. The perhydropyrene component of the feed mixture was relatively inert, but it could not be established whether this was due to a molecular sleve effect or intrinsic chemical kinetics factors.

Research Organization:
Chemical Engineering Department, University of Wyoming, Laramie, Wyoming 82071
DOE Contract Number:
AC22-77ET10651
OSTI ID:
5613993
Journal Information:
Ind. Eng. Chem. Process Des. Dev.; (United States), Journal Name: Ind. Eng. Chem. Process Des. Dev.; (United States) Vol. 22:3; ISSN IEPDA
Country of Publication:
United States
Language:
English