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Coking, aging, and regeneration of zeolites. III. Comparison of the deactivation modes of H-mordenite, HZSM-5, and HY during n-heptane cracking

Journal Article · · J. Catal.; (United States)

The rates of deactivation by carbonaceous residues (coke) of HY, H-mordenite, and HZSM-5, which have similar initial activities in n-heptane cracking are quite different: HZSM-5 forms very little coke and is very stable, while HM deactivates much faster than HY. The deactivation mechanisms of these zeolites could be specified by comparing as a function of the coke content: (i) the cracking activity of these zeolites and their capacity for adsorption of n-hexane, (ii) the volume apparently and really occupied by coke, and (iii) the number of coke molecules and of sites on which NH/sub 3/ can no longer be adsorbed. On HY, polyaromatic molecules are very rapidly formed on the strongest acid sites, these molecules obstructing partially or completely the access of the reactant to the acid sites. On HZSM-5 deactivation is initially due to the coverage of the acid sites, located at channel intersections, by alkylaromatics with 1 or 2 rings; later on (above 3% coke content) polyaromatic molecules, formed on the external surface, block access to a part of the pore volume. On HM deactivation is due to pore blockage: even at very low coke contents (1% coke), coke can block the access of n-heptane to a pore volume 10 times greater than the volume really occupied by the coke.

Research Organization:
Universite de Poitiers (France)
OSTI ID:
5269482
Journal Information:
J. Catal.; (United States), Journal Name: J. Catal.; (United States) Vol. 106:1; ISSN JCTLA
Country of Publication:
United States
Language:
English