Catalytic performance of various mesoporous silicas modified with copper or iron oxides introduced by different ways in the selective reduction of NO by ammonia

被引:130
作者
Chmielarz, L
Kustrowski, P
Dziembaj, R
Cool, P
Vansant, EF
机构
[1] Jagiellonian Univ, Fac Chem, PL-30060 Krakow, Poland
[2] Univ Antwerp, Dept Chem, Inorgan Chem Lab, B-2610 Antwerp, Belgium
关键词
mesoporous silicas; copper; iron; DeNO(x); NH3;
D O I
10.1016/j.apcatb.2005.09.004
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
Mesoporous silicas (MCM-48, SBA-15, MCF), reflecting various porous structures, were modified with copper andiron oxides by two different methods. For a first series of the samples the molecular designed dispersion (MDD) method using acetylacetonate complexes of copper and iron was applied for the deposition of transition metal oxides on the silica supports. A second series of the catalysts was obtained by the incipient impregnation technique using aqueous solutions of the suitable metal nitrates. The modified materials were characterized with respect to the texture (BET), composition (electron microprobe analysis), coordination of the transition metals (UV-vis-DRS) and surface acidity (NH3-TPD, FTIR). The mesoporous silica supports modified with transition metal oxides were tested as catalysts of the selective reduction of NO with ammonia. The catalytic performance of the studied samples depended on the method used for the deposition of transition metal oxide as well as the kind of mesoporous silica used as a catalytic support. In general, the Cu-containing mesoporous samples effectively operated at lower temperatures than silicas modified with iron. The samples obtained by the MDD method have been found to be more active and selective compared to the analogous samples prepared by the impregnation technique. An introduction of water vapor into the reaction mixture only slightly decreased the NO conversion and selectivity towards N-2 over the MCF mesoporous silica modified with copper or iron oxide. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:369 / 380
页数:12
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