TY - JOUR
T1 - Comparative study of the catalytic properties of ZSM-22 and ZSM-35/ferrierite zeolites in the skeletal isomerization of 1-butene
AU - Byggningsbacka, R.
AU - Kumar, N.
AU - Lindfors, L. E.
N1 - Funding Information:
Financial support from the Finnish Graduate School in Chemical Engineering (GSCE) is gratefully acknowledged.
Copyright:
Copyright 2018 Elsevier B.V., All rights reserved.
PY - 1998
Y1 - 1998
N2 - The catalytic activities of the two catalysts ZSM-22 and ZSM-35 were compared in the skeletal isomerization of 1-butene. ZSM-22 demonstrated higher activity in 1-butene transformation, compared to that of ZSM-35. ZSM-35 was not selective to isobutene until non-selective acid sites had been poisoned by coke deposits, while ZSM-22 was selective already from the beginning. Information about the extent of coke formation was obtained by FTIR experiments and surface area measurements. ZSM-22 was more resistant towards coke formation, compared to that of ZSM-35. In order to obtain information about the reaction mechanism, 2,4,4-trimethyl-2-pentene and 1-octene were cracked over the catalysts. The selective mechanism for isobutene formation in the skeletal isomerization of 1-butene was most likely monomolecular. The bimolecular mechanism is not selective to isobutene, although it can contribute to the overall isobutene production.
AB - The catalytic activities of the two catalysts ZSM-22 and ZSM-35 were compared in the skeletal isomerization of 1-butene. ZSM-22 demonstrated higher activity in 1-butene transformation, compared to that of ZSM-35. ZSM-35 was not selective to isobutene until non-selective acid sites had been poisoned by coke deposits, while ZSM-22 was selective already from the beginning. Information about the extent of coke formation was obtained by FTIR experiments and surface area measurements. ZSM-22 was more resistant towards coke formation, compared to that of ZSM-35. In order to obtain information about the reaction mechanism, 2,4,4-trimethyl-2-pentene and 1-octene were cracked over the catalysts. The selective mechanism for isobutene formation in the skeletal isomerization of 1-butene was most likely monomolecular. The bimolecular mechanism is not selective to isobutene, although it can contribute to the overall isobutene production.
UR - http://www.scopus.com/inward/record.url?scp=0000223430&partnerID=8YFLogxK
U2 - 10.1006/jcat.1998.2174
DO - 10.1006/jcat.1998.2174
M3 - Article
AN - SCOPUS:0000223430
SN - 0021-9517
VL - 178
SP - 611
EP - 620
JO - Journal of Catalysis
JF - Journal of Catalysis
IS - 2
M1 - CA982174
ER -