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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
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 Stepanov Alexander G. 1 , Luzgin Mikhail V. 1 , Sidelnikov Vladimir N. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Branch of the Russian Academy of Sciences, Prospekt Akademika Lavrentieva 5, Novosibirsk 630090, Russia

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
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
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Scopus 2
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