Combined XPS and in situ DRIRS study of mechanism of Pd-Fe/α-Al2O3 catalyzed CO coupling reaction to diethyl oxalate

被引:32
作者
Gao, ZH
Liu, ZC
He, F
Xu, GH
机构
[1] Tianjin Univ, Sch Sci, Dept Chem, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Sch Chem Engn & Technol, Tianjin 300072, Peoples R China
关键词
reaction mechanism; CO coupling reaction; diethyl oxalate (DEO); Pd-Fe/alpha-Al2O3; catalyst; X-ray photoelectron spectroscopy (XPS); diffuse reflectance infrared spectroscopy (DRIRS);
D O I
10.1016/j.molcata.2005.03.003
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 mechanism for the reaction of CO coupling to diethyl oxalate (DEO) over Pd-Fe/alpha-Al2O3 in gaseous phase at normal pressure was studied by X-ray photoelectron spectroscopy (XPS) and in situ diffuse reflectance infrared spectroscopy (DRIRS) techniques. The adsorption of two reactants, carbon monoxide and ethyl nitrite, on the catalyst was observed, respectively with in situ DRIRS as well as the catalysts after ethyl nitrite adsorption and after in situ reaction were also characterized by XPS measurement. These observational results show that (1) The ethyl nitrite on the catalyst surface has a dissociative chemisorption which leads to the oxidation of Pd-0 to Pd2+ (active component on the catalyst). So the reaction is a redox process; (2) Two intermediates, palladium complexes, in the reaction process are involved. From this, the mechanism steps of the reaction were proposed and the two intermediates were inferred. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:143 / 149
页数:7
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