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...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Journal of catalysis 2008-02, Vol.254 (1), p.71-78
Hauptverfasser: CAMPO, Betiana, PETIT, Corinne, VOLPE, Maria A
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
Beschreibung
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]
ISSN:0021-9517
1090-2694
DOI:10.1016/j.jcat.2007.11.018