Influence of the physico-chemical properties of CeO2-ZrO2 mixed oxides on the catalytic oxidation of NO to NO2

被引:74
作者
Atribak, Idriss [1 ]
Guillen-Hurtado, Noelia [1 ]
Bueno-Lopez, Agustin [1 ]
Garcia-Garcia, Avelina [1 ]
机构
[1] Univ Alicante, Fac Sci, Dept Inorgan Chem, MCMA Grp, Alicante 03690, Spain
关键词
Ceria-zirconia; Mixed oxides; Ceria; XPS; NO to NO2 oxidation capacity; SOLID-SOLUTIONS; TETRAGONAL ZIRCONIA; SURFACE; TRANSITION; STABILITY;
D O I
10.1016/j.apsusc.2010.06.042
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
Commercial and home-made Ce-Zr catalysts prepared by co-precipitation were characterised by XRD, Raman spectroscopy, N-2 adsorption at -196 degrees C and XPS, and were tested for NO oxidation to NO2. Among the different physico-chemical properties characterised, the surface composition seems to be the most relevant one in order to explain the NO oxidation capacity of these Ce-Zr catalysts. As a general trend, Ce-Zr catalysts with a cerium-rich surface, that is, high XPS-measured Ce/Zr atomic surface ratios, are more active than those with a Zr-enriched surface. The decrease in catalytic activity of the Ce-Zr mixed oxided upon calcinations at 800 degrees C with regard to 500 degrees C is mainly attributed to the decrease in Ce/Zr surface ratio, that is, to the surface segregation of Zr. The phase composition (cubic or t '' for Ce-rich compositions) seems not to be a direct effect on the catalytic activity for NO oxidation in the range of compositions tested. However, the formation of a proper solid solution prevents important surface segregation of Zr upon calcinations at high temperature. The effect of the BET surface area in the catalytic activity for NO oxidation of Ce-Zr mixed oxides is minor in comparison with the effect of the Ce/Zr surface ratio. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:7706 / 7712
页数:7
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