Investigations on the reaction mechanism of the skeletal isomerization of n-butenes to isobutene Part II. Reaction mechanism on ferrierites

Citation
D. Rutenbeck et al., Investigations on the reaction mechanism of the skeletal isomerization of n-butenes to isobutene Part II. Reaction mechanism on ferrierites, APP CATAL A, 208(1-2), 2001, pp. 153-161
Citations number
51
Categorie Soggetti
Physical Chemistry/Chemical Physics","Chemical Engineering
Journal title
APPLIED CATALYSIS A-GENERAL
ISSN journal
0926860X → ACNP
Volume
208
Issue
1-2
Year of publication
2001
Pages
153 - 161
Database
ISI
SICI code
0926-860X(20010214)208:1-2<153:IOTRMO>2.0.ZU;2-Q
Abstract
Ferrierites with Si/Al ratios between 20 and 70 were tested as catalysts fo r the skeletal isomerization of n-butenes to isobutene in the temperature r ange from 573 to 773 K. After 10 min time on stream (TOS) selectivities to isobutene between 50 and 92% were obtained, after 6h between 73 and 96%. de pending on the Si/Al ratio of the samples, the conversion of n-butenes and the reaction temperature. A clear trend of increasing selectivity to isobut ene with increasing Si/Al ratio, increasing temperature, and decreasing con version of n-butenes was observed. Furthermore, the coke content of the sam ples after reaction was determined. It was to low for a pore blockage of th e samples with Si/Al ratios >40. The results are discussed considering the different reaction mechanisms for the isomerization of n-butenes to isobute ne proposed in the literature. The monomolecular mechanism is assumed to be the main reaction path for the formation of isobutene on ferrierites. TPAD experiments established that the selectivity to isobutene is influenced ra ther by the number of acid sites than by the acid strength. (C) 2001 Elsevi er Science B.V. All rights reserved.