Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
9608016 | Applied Catalysis A: General | 2005 | 8 Pages |
Abstract
The hydroconversion of cyclohexene (CHE) using catalysts containing 0.35 wt.% of either Pt, Pd, Ir or Re on H-ZSM-5 support as well as the unloaded H-ZSM-5 zeolite was carried out using a flow-type fixed-bed reactor in a continuous flow of H2 gas. The hydroconversion of CHE was found to include its hydrogenation to CHA, dehydrogenation to benzene through cyclohexadienes (CHDEs) as intermediates, its isomerisation to the C5 ring containing cycloolefins (methylcyclopentenes, MCPEs) followed by their hydrogenation to methylcyclopentane (MCPA). Moreover, hydrocracking and alkylation products (toluene and xylenes) were found to form at higher temperatures. Hydrogenation and dehydrogenation reactions not only took place on the metal sites, but also on the unloaded zeolite at comparatively higher temperatures. The hydrogenation/dehydrogenation activities of the current metals were found to be in the order: Pd > Pt > Ir > Re. However, rhenium was almost catalytically inactive on all hydroconversion steps.
Keywords
Related Topics
Physical Sciences and Engineering
Chemical Engineering
Catalysis
Authors
Ahmed K. Aboul-Gheit, Sameh M. Aboul-Fotouh, Noha A.K. Aboul-Gheit,