T. Komatsu et al., Selective formation of alkenes through the cracking of n-heptane on Ca2+-exchanged ferrierite, APP CATAL A, 214(1), 2001, pp. 103-109
The cracking of n-heptane was carried out as a model reaction of naphtha cr
acking by using various zeolite catalysts to obtain light alkenes. such as
ethylene. propylene and butenes. with high selectivity at high conversion l
evels. The selectivity of zeolites having pore openings of 10 and 12-member
ed rings was compared at 80% conversion. H-ZSM-5 and H-ferrierite gave high
er alkene selectivity than H-MCM-22. H-mordenite. H-beta and H-Y. The effec
t of exchanged cations on the alkene selectivity was also examined with H-Z
SM-5 and H-ferrierite. Ca2+ or Ba2+-exchanged ferrierite gave the highest s
electivity to alkenes, 60 C-% at 70%; conversion. The Ca2+-exchange effecti
vely suppressed the secondary hydride transfer that would consume alkenes t
o form hydrogen-deficient species. As a result, the coke formation from the
hydrogen deficient species was also suppressed on Ca2+-exchanged ferrierit
e. which did not exhibit the rapid deactivation with time-on-stream. (C) 20
01 Elsevier Science B.V. All rights reserved.