Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts
The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 degrees C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main...
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Veröffentlicht in: | Journal of catalysis 2008-02, Vol.254 (1), p.71-78 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 degrees C over Au catalysts supported on ceria with low and medium surface areas (150 and 80 m2 g-1, respectively). An initial deactivation period was observed, followed by a steady-state regime. Ethanol was the main product in the deactivation period, whereas crotyl alcohol, butanal, butanol, and condensation products were produced under steady-state conditions. The activity and selectivity to crotyl alcohol (in the 20-32% range) were lower than those for the high-surface area ceria catalysts studied previously [B. Campo, M. Volpe, S. Ivanova, R. Touroude, J. Catal. 242 (2006) 162]. Samples were characterized by TPR, XPS, TEM, and XRD. The analysis of catalytic and characterization results indicates that gold particles supported on low- and medium-surface area ceria were relatively large, and the promotional effect of Ce3+ species was not achieved for the corresponding catalysts. Moreover, under reductive conditions, sintering still increased gold particle size. [PUBLICATION ABSTRACT] |
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ISSN: | 0021-9517 1090-2694 |
DOI: | 10.1016/j.jcat.2007.11.018 |