Decomposition of nitrous oxide by rhodium catalysts: Effect of rhodium particle size and metal oxide support

被引：57

作者：

Beyer, Hans ^{[1
]}

Emmerich, Jens ^{[1
]}

Chatziapostolou, Konstantinos ^{[1
]}

Koehler, Klaus ^{[1
]}

机构：

[1] Tech Univ Munich, Dept Chem, Ctr Catalysis Res, D-85747 Garching, Germany

来源：

APPLIED CATALYSIS A-GENERAL | 2011年 / 391卷 / 1-2期

关键词：

N2O; Decomposition; Rhodium catalyst; Particle size; Metal oxide support; ISOTOPIC EXCHANGE; N2O DECOMPOSITION; MOBILITY;

D O I：

10.1016/j.apcata.2010.03.060

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 catalytic decomposition of N2O by small rhodium particles (0.5-4.0 nm in diameter) supported on magnesia, silica, ceria, alumina and titania was studied in the absence and presence of oxygen. The impact of the use of rhodium chloride for catalyst preparation was also investigated. Rh/MgO and Rh/SiO2 are highly active catalysts for the decomposition of N2O at low reaction temperatures (200-300 degrees C), even in the presence of oxygen. The superior catalytic performance of Rh/MgO and Rh/SiO2 compared to Rh/CeO2. Rh/Al2O3 and Rh/TiO2 is attributed to relatively large rhodium particles (d(m), = 2.1-2.4 nm) present in the more active catalysts compared to very small ones (d(m) = 1.0-1.4 nm) present in the other catalysts. The degree of inhibition caused by excess oxygen in the feed gas and the impact of chloride ions on the catalytic activity are found to vary with the acid-base properties of the support materials and their influence on the redox properties of the active metal. Both inhibitory effects seem to be interconnected and rise in the same order as the basicity of the support materials. (C) 2010 Elsevier B.V. All rights reserved.

引用

页码：411 / 416

页数：6

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