Spectroscopic and surface potential variations study of a CuCe oxide catalyst using H2S as a probe molecule

被引:9
|
作者
Aboukaïs, A
Galtayries, A
Abi-Aad, E
Courcot, D
Grimblot, J
机构
[1] Univ Littoral Cote Opale, Lab Catalyse & Environm, MREID, EA 2598, F-59140 Dunkerque, France
[2] Univ Sci & Technol Lille, Lab Catalyse Heterogene & Homogene, CNRS, URA 402, F-59655 Villeneuve Dascq, France
关键词
CuCe oxide catalysts; H2S adsorption; XPS; EPR; surface potential variations;
D O I
10.1016/S0927-7757(98)00880-2
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
X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), electron paramagnetic resonance (EPR) and surface potential variations were used to study the reactivity of H2S on CuCe oxide catalyst. In the fresh catalyst, Cu2+ ions are present as monomers, dimers and clusters. After the H2S treatment at 293 K, all the Cu2+ species of catalyst become reduced. Such a reduction is irreversible even in the presence of oxygen. In parallel, S2- and SH- groups associated with copper in CeO2 are formed. Sulphide groups are stable and cannot be removed by further O-2 treatment. The valence of Ce(IV) is not affected with this H2S treatment. (C) 1999 Elsevier Science B.V. All rights reserved.
引用
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页码:335 / 342
页数:8
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