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Mechanism of the Isomerization of 1-Alkene during Iron-Catalyzed Fischer–Tropsch Synthesis

The deuterium/hydrogen exchange reaction was performed under iron-catalyzed Fischer–Tropsch reaction conditions using a mixture of deuterated octane, nonane, decane, tridecane, and pentadecane as the probes. The results indicated that deuterium/hydrogen exchange does not occur in alkanes under these...

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Bibliographic Details
Published in:Journal of catalysis 2001-04, Vol.199 (2), p.202-208
Main Authors: Shi, Buchang, O'Brien, Robert J, Bao, Shiqi, Davis, Burtron H
Format: Article
Language:English
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Summary:The deuterium/hydrogen exchange reaction was performed under iron-catalyzed Fischer–Tropsch reaction conditions using a mixture of deuterated octane, nonane, decane, tridecane, and pentadecane as the probes. The results indicated that deuterium/hydrogen exchange does not occur in alkanes under these conditions. Under the same reaction conditions, 1-octene-d16 was used as the probe to study the isomerization of 1-alkene. The 1-octene-d16 was reduced to deuterated octane, and isomerized to deuterated trans-2-octene and cis-2-octene with approximately equal amounts of the two isomers. No other internal deuterated octene and C7 products were obtained. The deuterium/hydrogen exchange reaction occurred in deuterated 1-octene as well as in the products formed from it. The maximum number of deuterium atoms that can be replaced by hydrogen is 5. There is no C8D16 isotopomer of 2-octenes. To account for these experimental facts, a mechanism was proposed for the isomerization of 1-alkene under iron-catalyzed Fischer–Tropsch reaction conditions.
ISSN:0021-9517
1090-2694
DOI:10.1006/jcat.2001.3175