Abstrakti
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.
| Alkuperäiskieli | Englanti |
|---|---|
| Artikkeli | CA982174 |
| Sivut | 611-620 |
| Sivumäärä | 10 |
| Julkaisu | Journal of Catalysis |
| Vuosikerta | 178 |
| Numero | 2 |
| DOI - pysyväislinkit | |
| Tila | Julkaistu - 1998 |
| OKM-julkaisutyyppi | A1 Julkaistu artikkeli, soviteltu |
Rahoitus
Financial support from the Finnish Graduate School in Chemical Engineering (GSCE) is gratefully acknowledged.
Sormenjälki
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