期刊
CHEMCATCHEM
卷 12, 期 17, 页码 4297-4303出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cctc.202000701
关键词
Cerium; Nitrogen oxide; NO direct decomposition; Perovskite
资金
- National Natural Science Foundation of China [51702230]
- program of Innovative Research Teams in Universities [IRT 0641]
NO direct decomposition is the most promising but also the most challenging approach for nitrogen oxides mitigation. Developing high performance catalysts is greatly desirable to promote the application of this technology. The present catalysts BaCoO3-CeO(2)prepared by the one-pot method show superior activity towards NO direct decomposition, robust oxygen resistance and decent durability. The NO conversion to N(2)of 5 %BaCoO3-CeO(2)catalyst is 57.2 %, 70.1 % and 75.6 % at 700, 750 and 800 degrees C, respectively. It still maintains at 54.3 % even in the presence of 10 vol % O(2)at 800 degrees C and is stable in 1 vol % O(2)at least for 24 h at 750 degrees C. Such impressive performance is ascribed to the unique properties of CeO2, strong interaction between perovskite and CeO2, and microstructure of the catalysts rendered by the citric acid-nitrate one-pot method.
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