N2O origin in NO reduction with NH3 over copper zeolites

被引:1
|
作者
Delahay, G
Kieger, S
Neveu, B
Coq, B
机构
[1] ENSCM, UMR CNRS 5618, Lab Mat Catalyt & Catalyse Chim Organ, F-34296 Montpellier, France
[2] Grande Paroisse SA, F-92062 Paris, France
来源
COMPTES RENDUS DE L ACADEMIE DES SCIENCES SERIE II FASCICULE C-CHIMIE | 1998年 / 1卷 / 04期
关键词
oxidation; ammonia; nitrogen oxides; zeolite; copper;
D O I
10.1016/S1387-1609(98)80039-X
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Ammonia oxidation has been studied between 298 to 800 K on zeolite NaY and copper-based catalysts (Cu(x)-NaY, x being the exchange degree). The main product of the reaction was N-2. The rates of NH3 conversion in selective catalytic reduction (SCR) of NO by NH3 (NH3 + O-2 + NO) and in NH3 oxidation (NH3 + O-2) were similar on Cu (195)-NaY, but differed at lower temperature on Cu(76)-NaY. On Cu(25)-NaY, the rate of NH(3 )conversion in SCR of NO was always much faster. During the SCR of NO on Cu(76)-NaY, two waves of N(2)O( )formation were observed, while on Cu(25)-NaY, no N2O was detected. The formation of N2O at low temperature was ascribed to the decomposition of ammonium nitrate formed on CuO aggregates. The second N2O formation at a higher temperature resulted from the ammonia oxidation which occurred either on next-neighbour isolated Cu2+ Or On [CuOCu](2+) dimers. (C) Academie des Sciences/Elsevier, Paris.
引用
收藏
页码:229 / 235
页数:7
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