Studies of sol-gel TiO2 and Pt/TiO2 catalysts for NO reduction by CO in an oxygen-rich condition

被引:55
作者
Wang, JA
Cuan, A
Salmones, J
Nava, N
Castillo, S
Morán-Pineda, M
Rojas, F
机构
[1] Inst Mexicano Petr, Programa Tratamiento Crudo Maya, Mexico City 07730, DF, Mexico
[2] Inst Politecn Nacl, ESIQIE, Lab Catalisis & Mat, Mexico City 07738, DF, Mexico
[3] Inst Mexicano Petr, Programa Ingn Mol, Mexico City 07730, DF, Mexico
[4] Univ Autonoma Metropolitana Iztapalapa, Dept Quim, Mexico City 09340, DF, Mexico
关键词
titania; NO reduction; sol-gel synthesis; PL/TiO2; catalysts;
D O I
10.1016/j.apsusc.2004.02.057
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 textural properties, morphological features, surface basicity and oxygen reduction behaviours of titania and Pt supported titania catalysts synthesized via a sol-gel method were studied by means of N-2 physisorption, SEM, TEM, CO2-TPD and H-2-TPR techniques. Mesostructured TiO2 shows a very narrow pore size distribution that uniformly centred at about 4 nm. High resolution TEM images confirmed that most of Pt particles on Pt/TiO2-SG had a size smaller than 2 nm. Both the titania support and Pt loaded catalysts chiefly contained weak basic sites with small amount of strong basic sites. Loading Pt did not significantly alter the surface reduction characters of titania, indicating a weak interaction between Pt metals and titania support. Catalytic evaluation revealed that the selectivity of NO reduction over titania was insensitive to variation of textural property. On the bare titania, low NO conversion but high selectivity to N2O was obtained. However, the Pt/TiO2-SG catalysts exhibited high NO conversion and high selectivity to N-2, which is assumed to relate to NO dissociation catalysed by the metallic Pt clusters. In addition, when the reaction temperature was above 200 degreesC, 3-11% NO2 was yielded over the Pt/TiO2-SG catalysts, which was discussed on a basis of reaction competition, metal-support interaction and NO dissociation. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:94 / 105
页数:12
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