Title of article
Active coke: Carbonaceous materials as catalysts for alkane dehydrogenation
Author/Authors
James McGregor، نويسنده , , Zhenyu Huang، نويسنده , , Edward P.J. Parrott، نويسنده , , J. Axel Zeitler، نويسنده , , K. Lien Nguyen، نويسنده , , Jeremy M. Rawson، نويسنده , , Albert Carley، نويسنده , , Thomas W. Hansen، نويسنده , , Jean-Philippe Tessonnier، نويسنده , , Dang Sheng Su، نويسنده , , Detre Teschner، نويسنده , , Elaine M. Vass، نويسنده , , Axel Knop-Gericke، نويسنده , , R. Schlogl ، نويسنده , , Lynn F. Gladden، نويسنده ,
Issue Information
روزنامه با شماره پیاپی سال 2010
Pages
11
From page
329
To page
339
Abstract
The catalytic dehydrogenation (DH) and oxidative dehydrogenation (ODH) of light alkanes are of significant industrial importance. In this work both carbonaceous material deposited on VOx/Al2O3 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 VOx 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.
Keywords
Scanning transmission electron microscopy , Iridium complex catalyst , Single-atom imaging , Ethene hydrogenation
Journal title
Journal of Catalysis
Serial Year
2010
Journal title
Journal of Catalysis
Record number
1225879
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