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  Active coke: Carbonaceous materials as catalysts for alkane dehydrogenation

McGregor, J., Huang, Z., Parrott, E. P. J., Zeitler, J. A., Nguyen, K. L., Rawson, J. M., et al. (2010). Active coke: Carbonaceous materials as catalysts for alkane dehydrogenation. Journal of Catalysis, 269(2), 329-339. doi:10.1016/j.jcat.2009.11.016.

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 Creators:
McGregor, James, Author
Huang, Zhenyu, Author
Parrott, Edward P. J., Author
Zeitler, J. Axel, Author
Nguyen, K. Lien, Author
Rawson, Jeremy M., Author
Carley, Albert, Author
Hansen, Thomas W.1, Author           
Tessonnier, Jean-Philippe1, Author           
Su, Dang Sheng1, Author           
Teschner, Detre1, Author           
Vass, Elaine M.1, Author           
Knop-Gericke, Axel1, Author           
Schlögl, Robert1, Author           
Gladden, Lynn F., Author
Affiliations:
1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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Free keywords: Vanadia catalysts; Carbon nanofibres; THz time domain spectroscopy; Coke; Transmission electron microscopy; Butane dehydrogenation; X-ray absorption spectroscopy Research Context: Carbon
 Abstract: The catalytic dehydrogenation (DH) and oxidative dehydrogenation (ODH) of light alkanes are of significant industrial importance. In this work both carbonaceous materials 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.

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Language(s): eng - English
 Dates: 2010-02-05
 Publication Status: Issued
 Pages: -
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 Table of Contents: -
 Rev. Type: Peer
 Identifiers: eDoc: 443398
DOI: 10.1016/j.jcat.2009.11.016
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Title: Journal of Catalysis
  Alternative Title : J. Catal.
Source Genre: Journal
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Pages: - Volume / Issue: 269 (2) Sequence Number: - Start / End Page: 329 - 339 Identifier: -