The role of surface vanadia species in butane dehydrogenation over VOx/Al2O3

McGregor, J., Huang, Z., Shiko, G., Gladden, L. F., Stein, R. S., Duer, M. J., Wu, Z., Stair, P. C., Rugmini, S. and Jackson, S. D. (2009) The role of surface vanadia species in butane dehydrogenation over VOx/Al2O3. Catalysis Today, 142(3-4), pp. 143-151. (doi:10.1016/j.cattod.2008.07.022)

McGregor, J., Huang, Z., Shiko, G., Gladden, L. F., Stein, R. S., Duer, M. J., Wu, Z., Stair, P. C., Rugmini, S. and Jackson, S. D. (2009) The role of surface vanadia species in butane dehydrogenation over VOx/Al2O3. Catalysis Today, 142(3-4), pp. 143-151. (doi:10.1016/j.cattod.2008.07.022)

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Abstract

A series of theta-Al2O3 supported VOx catalysts, of different vanadium loadings, have been characterised and employed for the selective dehydrogenation of n-butane. Characterisation of the unreacted catalysts has been carried out by solid-state NMR (V-51 MAS NMR, Al-27 MAS NMR and Al-27 3Q-MAS NMR), and FT-IR spectroscopies, with reference to previously acquired Raman and UV-vis spectroscopy data. As vanadium loading increases, so does the domain size of the Supported vanadate units with significant quantities of V2O5 observed at the highest loadings. The influence of calcination, pre-reduction, reaction and regeneration on the structure of the catalysts has been studied by NMR, FT-IR, EPR, microanalysis and TEOM. Calcination disperses crystalline vanadate units, and at high loadings AlVO4 formation is observed. Pre-reduction reduces the vanadium oxidation state from 5+ to 3+, while regeneration results in the formation of highly crystalline V5+ species. From these data it is possible to determine structure-activity relationships, with polymeric vanadia Clusters favouring the formation of butenes and butadienes, while more isolated species are highly active towards the formation of polynuclear aromatic hydrocarbons retained on the catalyst surface post-reaction. These large polynuclear aromatic hydrocarbons are however not the principle cause of catalyst deactivation in this reaction. .

Item Type:Articles
Keywords:AL-27 Alkane dehydrogenation AMMONIUM METAVANADATE AROMATIC-HYDROCARBON CATALYST CATALYSTS CLUSTER CLUSTERS Deactivation DEHYDROGENATION DOMAIN FTIR GAMMA-ALUMINA MAS NMR NMR OXIDATION Oxidation kinetics OXIDATIVE DEHYDROGENATION Polynuclear PYROPHOSPHATE CATALYST RAMAN-SPECTROSCOPY SOLID-STATE SOLID-STATE NMR SPECTROSCOPY STATE STATE V-51 NMR Structure SUPPORTED METAL-OXIDE SURFACE THERMAL-DECOMPOSITION UNIT UNITS V/THETA-AL2O3 CATALYSTS Vanadia catalysts vanadium VIBRATIONAL-SPECTRA
Status:Published
Refereed:Yes
Glasgow Author(s) Enlighten ID:Rugmini, Dr Sreekala and Jackson, Professor Samuel
Authors: McGregor, J., Huang, Z., Shiko, G., Gladden, L. F., Stein, R. S., Duer, M. J., Wu, Z., Stair, P. C., Rugmini, S., and Jackson, S. D.
College/School:College of Science and Engineering > School of Chemistry
Journal Name:Catalysis Today
ISSN:0920-5861

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