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The kinetics of the catalytic isomerization and transalkylation of cumene

Journal Article · · J. Catal.; (United States)
New and previously published kinetic data for cumene cracking on lanthanum Y zeolite were used to determine the initial rates and selectivities for the primary products benzene, n-propylbenzene, cymene, m-diisopropyl benzene, p-diisopropyl benzene, isobutene, and butene at 360/sup 0/-500/sup 0/. An analysis of the activation energies and frequency factors shows that the addition of a methyl group of one cumene molecule to the benzene ring of another to form cymene is energetically favored over the insertion of the methyl group into an isopropyl side chain; that, in the formation of butenes by transfer of a methyl group from one cumene molecule to the isopropropyl group of another, the addition to the ..cap alpha..-carbon is energetically favored over additon to the ..beta..-carbon (i.e., that isobutene is the favored product); that in the disproportionation of cumene to benzene and diisopropyl benzene the meta form is the main product at 500/sup 0/C as a result of entropy (or configurational) requirements, and that at room temperature the para form is favored by the activation energy; and that the isomerization of cumene to n-propylbenzene requires almost complete rupture of the side chain. Graph and tables.
Research Organization:
Queens Univ., Kingston, Canada
OSTI ID:
5872837
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 53:2; ISSN JCTLA
Country of Publication:
United States
Language:
English