Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Reactions of methylcyclohexane and n-heptane over supported Pt and Pt-Re catalysts

Journal Article · · J. Catal.; (United States)
Reactions of methylcyclohexane (MCH) and n-heptane were compared, using industrial Pt/Al/sub 2/O/sub 3/ or Pt-Re/Al/sub 2/O/sub 3/ catalysts. Although the same products were generally observed, product selectivity and rate of catalyst deactivation differed substantially for the two reactants. With n-heptane, greater amounts of light cracked products (C/sub 1/-C/sub 5/), heavy alkylated aromatics, and coke were produced. With n-heptane the total aromatic yield (benzene + toluene yields) was substantially less and the decline in the total aromatic yield during the first feed cycle was in general much greater. Selectivity for aromatic products immediately following hydrogen treatment of the coked Pt-Re catalysts was less with MCH than with n-heptane. Presulfiding the Pt catalyst slightly poisoned the dehydrogenation and dehydrocyclization activities. However, the presulfided Pt-Re/Al/sub 2/O/sub 3/ catalyst was very selective for these reactions and a high total aromatic yield was observed with either MCH or n-heptane. Sulfur quenched hydrogenolysis, demethylation, and reactions which form alkylated aromatics of higher molecular weight than toluene.
Research Organization:
Univ. of Connecticut, Storrs (USA)
OSTI ID:
5327715
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 107:2; ISSN JCTLA
Country of Publication:
United States
Language:
English