Olefin as an Intermediate in n-Butane Isomerization on Sulfated Zirconia. An in situ 13C MAS NMR Study of n-Octene-1 Conversion Full article
Journal |
Catalysis Letters
ISSN: 1011-372X , E-ISSN: 1572-879X |
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Output data | Year: 2002, Volume: 78, Number: 1-4, Pages: 153-156 Pages count : 4 DOI: 10.1023/A:1014933623857 | ||
Tags | 13C MAS NMR, Alkanes, Cyclopentenyl cations, Isomerization, N-octene-1, Sulfated zirconia | ||
Authors |
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Affiliations |
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Funding (1)
1 | Russian Foundation for Basic Research | 99-03-32454 |
Abstract:
By using in situ13C MAS NMR and ex situ GC-MS, the analysis of hydrocarbon products formed from n-octene-1 adsorbed on sulfated zirconia catalyst (SZ) has been performed. It is shown that a mixture of alkanes and stable alkyl substituted cyclopentenyl cations (CPC) is formed as the basic reaction products. Formation of both alkanes and CPC from n-octene-1, a precursor of C8+ cation, the key intermediate in n-butane isomerization via a “bimolecular pathway”, implies that formation of the isomerized alkane occurs by a complex process of “conjunct polymerization”, rather than isomerization itself. CPC deposited on the SZ surface can be in charge of the catalyst deactivation.
Cite:
Stepanov A.G.
, Luzgin M.V.
, Sidelnikov V.N.
Olefin as an Intermediate in n-Butane Isomerization on Sulfated Zirconia. An in situ 13C MAS NMR Study of n-Octene-1 Conversion
Catalysis Letters. 2002. V.78. N1-4. P.153-156. DOI: 10.1023/A:1014933623857 WOS Scopus РИНЦ ANCAN OpenAlex
Olefin as an Intermediate in n-Butane Isomerization on Sulfated Zirconia. An in situ 13C MAS NMR Study of n-Octene-1 Conversion
Catalysis Letters. 2002. V.78. N1-4. P.153-156. DOI: 10.1023/A:1014933623857 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: | Apr 24, 2001 |
Accepted: | Oct 3, 2001 |
Published print: | Mar 1, 2002 |
Identifiers:
Web of science: | WOS:000175691600024 |
Scopus: | 2-s2.0-0036488986 |
Elibrary: | 13392318 |
Chemical Abstracts: | 2002:405445 |
Chemical Abstracts (print): | 137:142153 |
OpenAlex: | W179015518 |