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  The role and structure of carbonaceous materials in dehydrogenation reactions

McGregor, J., Zeitler, J. A., Parrott, E. P. J., Gladden, L. F., Tessonnier, J.-P., Hansen, T. W., et al. (2009). The role and structure of carbonaceous materials in dehydrogenation reactions. Talk presented at 21st NAM (North American Catalysis Society Meeting). San Francisco, California [USA]. 2009-06-07 - 2009-06-12.

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McGregorNACS-1c_1.pdf (Preprint), 67KB
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 Creators:
McGregor, James1, Author           
Zeitler, J. Axel, Author
Parrott, Edward P. J., Author
Gladden, Lynn F., Author
Tessonnier, Jean-Philippe1, Author           
Hansen, Thomas W.1, Author           
Su, Dang Sheng1, Author           
Schlögl, Robert1, Author           
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1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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Free keywords: Carbon; ODH; VOx/Al2O3; Catalyst Carbon
 Abstract: The catalytic dehydrogenation (DH) and oxidative dehydrogenation (ODH) of light alkanes is widely studied as a route to the formation of alkenes and di-alkenes, important precursor molecules for synthetic rubbers, plastics and a variety of other products [1,2]. Recent studies have focused on the non-oxidative DH of butane over alumina-supported vanadia catalysts [3-5]. In the present work, we provide a detailed understanding of both the role and structure of coke deposited on VOx/Al2O3 during reaction. A range of characterisation techniques have been employed including the first application of terahertz time domain spectroscopy (THz-TDS) to the study of coke. Complementary THz-TDS characterisation of carbonaceous materials including carbon nanofibres (CNFs) has also been conducted. For such materials THz-TDS spectra can be correlated with their catalytic performance in the oxidative dehydrogenation of ethylbenzene to form styrene.

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Language(s): eng - English
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Title: 21st NAM (North American Catalysis Society Meeting)
Place of Event: San Francisco, California [USA]
Start-/End Date: 2009-06-07 - 2009-06-12

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