Hydrogenation of crotonaldehyde on different Au/CeO2 catalysts

被引:57
作者
Campo, Betiana [1 ]
Petit, Corinne [2 ]
Volpe, Maria A. [1 ]
机构
[1] PLAPIQUI, RA-8000 Bahia Blanca, Buenos Aires, Argentina
[2] ULP, ECPM, CNRS UMR 7515, LMSPC, F-67087 Strasbourg 2, France
关键词
gold; ceria; crotonaldehyde hydrogenation; selective hydrogenation;
D O I
10.1016/j.jcat.2007.11.018
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The gas-phase hydrogenation of crotonaldehyde was carried out at 120, 150, and 180 degrees C over An catalysts supported on ceria with low and medium surface areas (150 and 80 m(2) 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. (c) 2007 Elsevier Inc. All rights reserved.
引用
收藏
页码:71 / 78
页数:8
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