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  The structure and mechanistic impact of carbon deposits 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 structure and mechanistic impact of carbon deposits in dehydrogenation reactions. Talk presented at EuropaCat IX. Salamanca [Spain]. 2009-08-30 - 2009-09-04.

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McGregor_Ext_Europacat2009_2a.pdf (Preprint), 100KB
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 Urheber:
McGregor, James1, Autor           
Zeitler, J. Axel, Autor
Parrott, Edward P. J., Autor
Gladden, Lynn F., Autor
Tessonnier, Jean-Philippe1, Autor           
Hansen, Thomas W.1, Autor           
Su, Dang Sheng1, Autor           
Schlögl, Robert1, Autor           
Affiliations:
1Inorganic Chemistry, Fritz Haber Institute, Max Planck Society, ou_24023              

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Schlagwörter: Carbon, ODH, VOx/Al2O3, Catalyst Carbon
 Zusammenfassung: 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 [1-4]. Recent studies have focused on the non-oxidative DH of butane over alumina-supported vanadia catalysts [5-7]. 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.

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Sprache(n): eng - English
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 Identifikatoren: eDoc: 430066
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Titel: EuropaCat IX
Veranstaltungsort: Salamanca [Spain]
Start-/Enddatum: 2009-08-30 - 2009-09-04

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