Sammanfattning
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.
| Originalspråk | Engelska |
|---|---|
| Artikelnummer | CA982174 |
| Sidor (från-till) | 611-620 |
| Antal sidor | 10 |
| Tidskrift | Journal of Catalysis |
| Volym | 178 |
| Nummer | 2 |
| DOI | |
| Status | Publicerad - 1998 |
| MoE-publikationstyp | A1 Tidskriftsartikel-refererad |
Finansiering
Financial support from the Finnish Graduate School in Chemical Engineering (GSCE) is gratefully acknowledged.
Fingeravtryck
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