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In relation to this article, we declare that there is no conflict of interest.
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Received August 25, 2006
Accepted November 11, 2006
articles This is an Open-Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/bync/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
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Influences of A- or B-site substitution on the activity of LaMnO3 perovskite-type catalyst in oxidation of diesel particle

Key Laboratory for Thermal Science and Power Engineering of Ministry of Education,Department of Thermal Engineering, Tsinghua University, Beijing 100084, China
qsong@mail.tsinghua.edu.cn
Korean Journal of Chemical Engineering, May 2007, 24(3), 503-507(5), 10.1007/s11814-007-0088-5
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Abstract

LaMnO3 was partially substituted at A- or B-site by Sol-Gel method and characterized by XRD, SEM and BET. Perovskite oxides were formed in all substitutions. The catalytic activities of substituted catalysts on carbon black oxidation were measured by Temperature Programming Oxidation (TPO). Experimental results showed that all substitutions increased the catalytic activity of LaMnO3, and La0.8Cs0.2MnO3 showed the highest catalytic activity. Under tight contact, the activity enhancement of different substitutions decreased in the order Cs>K>V>Ce>Co>Cu>Fe. Dynamic analysis showed that partial substitutions increased the pre-exponential factor and the catalytic activity by increasing the oxygen vacancy on the catalyst surface. The active components on the surfaces of La0.8Ce0.2MnO3 and LaMn0.8V0.2O3 included CeO2 and LaVO4, which changed the apparent activities and dynamic parameters of these two catalysts.

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