FT-IR study of NO+O2 co-adsorption on H-ZSM-5:: re-assignment of the 2133 cm-1 band to NO+ species

被引:286
作者
Hadjiivanov, K
Saussey, J
Freysz, JL
Lavalley, JC
机构
[1] Univ Caen, ISMRA, UMR CNRS 6506, Catalyse & Spectrochim Lab, F-14050 Caen, France
[2] Bulgarian Acad Sci, Inst Gen & Inorgan Chem, BU-1113 Sofia, Bulgaria
关键词
nitrogen oxides; nitrosonium ion; DeNOx; H-ZSM-5; IR spectroscopy;
D O I
10.1023/A:1019059117488
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
Whereas NO adsorption at room temperature on activated H-ZSM-5 (Si/Al = 29) caused only negligible changes in its IR spectrum, addition on O-2 to NO led to the appearance of bands at 2133 and 977 cm(-1). Concomitantly, the number of acidic zeolite OH groups decreased while H2O hydrogen-bonded to zeolite OH groups developed. Introduction of small amounts of O-18(2) did not change the 2133 cm(-1) band wavenumber, nor the use of a partly deuteroxylated D-H-ZSM-5 sample. In such a case, HOD formation was detected. The results obtained evidence that the 2133 cm(-1) band, generally considered as characterizing NO2+ species, is, in fact, due to NO+ species occupying cationic positions in the zeolite. The 977 cm(-1) band is attributed to the O-lattice-NO+ vibration. A scheme of the NO+ formation, involving NO2 molecules as NO oxidizing agent, is proposed.
引用
收藏
页码:103 / 108
页数:6
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