Study of the influence of the In2O3 loading on γ-alumina for the development of de-NOx catalysts

被引:53
作者
Perdigon-Melon, JA
Gervasini, A
Auroux, A
机构
[1] Inst Rech Catalyse, CNRS, F-69626 Villeurbanne, France
[2] CSIC, Inst Quim Fis Rocasolano, E-28006 Madrid, Spain
[3] Univ Milan, Dipartimento Chim Fis & Elettrochim, I-20133 Milan, Italy
关键词
alumina-supported indium oxide; de-NOx catalysts; surface characterizations; redox and acid/base sites;
D O I
10.1016/j.jcat.2005.07.001
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
Alumina-supported indium oxide (In2O3) catalysts with In loadings between 2 and 22 wt% were prepared by impregnation and characterized for their main properties. Surface properties, such as the surface area; surface In content, measured by X-ray photoelectron spectroscopy (XPS); and acidity and basicity, measured both by adsorption microcalorimetry using ammonia and sulfur dioxide as probe molecules and by infrared spectroscopy of pyridine adsorption, were determined. Bulk properties, namely the crystallographic structure as determined by powder X-ray diffraction (XRD) analysis and the redox character of the In2O3-dispersed phase as determined by redox cycles performed both in a flow apparatus and in a thermobalance coupled with a differential scanning microcalorimeter (TG-DSC), were studied. The results obtained were interpreted in terms of In2O3 surface dispersion or aggregation. The catalysts tested in the reduction of NOx by ethene in an oxygen-rich atmosphere showed an interesting ability to selectively reduce NOx to N-2, independently of the In loading. The weakness of the oxidative properties of the In2O3 phases limited the ethene combustion and made the catalysts able to reduce NOx even at high temperature (up to 550 degrees C). The rates of nitrogen formation depended strongly on the In2O3 aggregation state; the In centers were very active even at low amounts. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:421 / 430
页数:10
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