Abstract
A series of copper rich CuPd/Al2O3 catalysts were prepared and characterised by FTIR spectroscopy using CO as a probe molecule. After reduction, the surface composition was largely composed of Cu with evidence of a small concentration of isolated Pd atoms. It was found that CO induced surface segregation could be used to increase the surface Pd concentration and depending on the Cu:Pd ratio, the formation of Pd–Pd dimers was possible. Changes in surface composition were quantified and correlated with catalyst activity and selectivity for selective acetylene hydrogenation. For the catalyst with optimum Cu:Pd ratio (50:1), it was possible to use CO induced segregation to increase activity considerably (20 K temperature reduction to achieve 100% conversion) whilst only marginally affecting ethylene selectivity (≈5% decrease in ethylene selectivity). An estimate of the detection limit by FTIR of the minimum surface coverage of isolated Pd and Pd–Pd dimers is given.
Original language | English |
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Pages (from-to) | 538-546 |
Number of pages | 9 |
Journal | Journal of Catalysis |
Volume | 329 |
Early online date | 25 Jul 2015 |
DOIs | |
Publication status | Published - Sept 2015 |
Bibliographical note
Date of Acceptance: 01/06/2015We thank the University of Aberdeen for financial support and A.I. McNab (University of Aberdeen) for discussions involving the calculation of surface sites.
Keywords
- copper
- palladium
- FTIR spectroscopy
- selective hydrogenation
- surface segregation