Active coke: Carbonaceous materials as catalysts for alkane dehydrogenation

Carbonaceous material deposited on VO x /Al 2O 3 is shown to provide the catalytically active sites for n-butane dehydrogenation at 973 K. The activity of carbon is confirmed through studies on carbon nanofibres. The catalytic dehydrogenation (DH) and oxidative dehydrogenation (ODH) of light alkanes...

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Veröffentlicht in:Journal of catalysis 2010-02, Vol.269 (2), p.329-339
Hauptverfasser: McGregor, James, Huang, Zhenyu, Parrott, Edward P.J., Zeitler, J. Axel, Nguyen, K. Lien, Rawson, Jeremy M., Carley, Albert, Hansen, Thomas W., Tessonnier, Jean-Philippe, Su, Dang Sheng, Teschner, Detre, Vass, Elaine M., Knop-Gericke, Axel, Schlögl, R., Gladden, Lynn F.
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Sprache:eng
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Zusammenfassung:Carbonaceous material deposited on VO x /Al 2O 3 is shown to provide the catalytically active sites for n-butane dehydrogenation at 973 K. The activity of carbon is confirmed through studies on carbon nanofibres. The catalytic dehydrogenation (DH) and oxidative dehydrogenation (ODH) of light alkanes are of significant industrial importance. In this work both carbonaceous material deposited on VO x /Al 2O 3 catalysts during reaction and unsupported carbon nanofibres (CNFs) are shown to be active for the dehydrogenation of butane in the absence of gas-phase oxygen. Their activity in these reactions is shown to be dependent upon their structure, with different reaction temperatures yielding structurally different coke deposits. Terahertz time-domain spectroscopy (THz-TDS), among other techniques, has been applied to the characterisation of these deposits – the first time this technique has been employed in coke studies. TEM and other techniques show that coke encapsulates the catalyst, preventing access to VO x sites, without a loss of activity. Studies on CNFs confirm that carbonaceous materials act as catalysts in this reaction. Carbon-based catalysts represent an important new class of potential catalysts for DH and ODH reactions.
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2009.11.016