Issue 1, 2013

Modifications of the metal and support during the deactivation and regeneration of Au/C catalysts for the hydrochlorination of acetylene

Abstract

The effect of the gold oxidation state and carbon structure on the activity of Au/C catalysts for the hydrochlorination of acetylene was investigated by a combined approach using TPR, XPS and porosimetry determinations. The activity of the catalyst in the synthesis of vinyl chloride monomer was found to be dependent on the presence of Au3+ species in the catalyst. However, by preparing catalysts with different Au3+ content it was possible to determine the existence of a threshold Au3+ amount, beyond which the excess of Au3+ was not active for the reaction. This was explained by the existence of active sites at the Au/C interface, and not just by the presence of Au3+ species on top of Au nanoparticles, as explained by current models for these catalysts. It was also possible to determine the existence of a subset of Au nanoclusters which do not take part in the reaction, as well as changes in the textural properties of the carbon that can affect its long term reusability.

Graphical abstract: Modifications of the metal and support during the deactivation and regeneration of Au/C catalysts for the hydrochlorination of acetylene

Supplementary files

Article information

Article type
Paper
Submitted
09 Jul 2012
Accepted
03 Aug 2012
First published
07 Aug 2012
This article is Open Access
Creative Commons BY license

Catal. Sci. Technol., 2013,3, 128-134

Modifications of the metal and support during the deactivation and regeneration of Au/C catalysts for the hydrochlorination of acetylene

M. Conte, C. J. Davies, D. J. Morgan, T. E. Davies, A. F. Carley, P. Johnston and G. J. Hutchings, Catal. Sci. Technol., 2013, 3, 128 DOI: 10.1039/C2CY20478A

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