Time-resolved in situ XANES study of the redox properties of Ce0.9Zr0.1O2 mixed oxides

被引:23
|
作者
Zimicz, M. G. [1 ]
Larrondo, S. A. [1 ,2 ]
Prado, R. J. [3 ]
Lamas, D. G. [4 ,5 ]
机构
[1] Ctr Invest Solidos CINSO CONICET CITEDEF, Villa Martelli, Pcia Buenos Air, Argentina
[2] FIUBA Buenos Aires, Depto Ing Quim, Lab Proc Catalit, Buenos Aires, DF, Argentina
[3] Univ Fed Mato Grosso, Inst Fis, BR-78060900 Cuiaba, MT, Brazil
[4] Univ Nacl Comahue, Fac Ingn, Lab Caracterizac Mat, RA-1400 Buenos Aires, DF, Argentina
[5] Consejo Nacl Invest Cient & Tecn, RA-1033 Buenos Aires, DF, Argentina
关键词
XANES; TPR; Reduction-reoxidation; Ce0.9Zr0.1O2; X-RAY-ABSORPTION; NEAR-EDGE STRUCTURE; OXIDATION-STATE; SPECTROSCOPY; CATALYSTS; METHANE; CERIUM; CEO2;
D O I
10.1016/j.ijhydene.2012.01.162
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 aim of this paper is to gain further insight in the reduction and reoxidation processes taking place when Ce0.9Zr0.1O2 mixed oxides are in reducing or oxidizing atmospheres, respectively. The reduction process of these mixed oxides synthesized by two stoichiometric nitrate-aminoacid gel-combustion routes using glycine and lysine as fuels is studied by conventional H-2-Temperature Programmed Reduction experiments. The results are compared with those obtained by time-resolved in situ X-ray absorption near-edge spectroscopy (XANES) in the energy level corresponding to the Ce L-III absorption edge. The reoxidation process by this last technique is also studied. Even though the identical composition and crystal structure of both samples, the redox processes resulted very different for each solid, suggesting the influence of specific surface area, pore volume and particle size on them. Copyright (C) 2012, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:14881 / 14886
页数:6
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