Effect of tin content and reduction temperature on the catalytic behaviour of PtSn/TiO2 catalysts in the vapour-phase hydrogenation of crotonaldehyde

J. Ruiz-Martinez, F. Coloma, A. Sepulveda-Escribanoa, J. A. Anderson, F. Rodriguez-Reinoso

Research output: Contribution to journalArticle

33 Citations (Scopus)

Abstract

This paper reports a study of PtSn/TiO2 catalysts reduced at two different temperatures (473 and 773 K) by infrared spectroscopy of CO adsorbed at 298 K and XPS, as well as their behaviour in the vapour phase selective hydrogenation of crotonaldehyde at 333 K. Catalysts with 2 wt% Pt and different Pt:Sn atomic ratios were prepared by co-impregnation of a commercial TiO2 (P25, from Degussa) with aqueous solutions of H2PtCl6 and SnCl2 center dot 2H(2)O. XPS results show that tin is in oxidized state when the catalysts are reduced at 473 K, whereas a proportion is in the metallic state after reduction at 773 K. The amount of surface platinum decreases when the tin loading and the reduction temperature increase. The presence of Pt-Sn alloy in the catalysts after reduction at high temperature has been assessed by in situ IR spectroscopy of adsorbed CO, although a proportion of platinum remains in a non-alloyed state. The catalytic activity in the vapour-phase hydrogenation of crotonaldehyde increases after high temperature reduction, and the same behaviour is obtained with selectivity towards the hydrogenation of the carbonyl bond to yield the unsaturated alcohol, the best selectivity being obtained for the catalyst with the lowest Pt/Sn ratio. (c) 2007 Elsevier B.V. All rights reserved.

Original languageEnglish
Pages (from-to)35-41
Number of pages7
JournalCatalysis Today
Volume133-135
Early online date10 Jan 2008
DOIs
Publication statusPublished - Apr 2008

Keywords

  • Pt-Sn catalysts
  • titania
  • crotonaldehyde hydrogenation
  • FTIR
  • PT-SN catalysts
  • pregraphitized carbon-black
  • infrared-spectra
  • CO adsorption
  • N-octane
  • platinum
  • dehydrocyclization
  • conversion
  • monoxide
  • surfaces

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