Selective catalytic reduction of nitrous oxide over Fe-ZSM-5: the effect of ion-exchange level

被引:42
作者
Yamada, K [1 ]
Kondo, S [1 ]
Segawa, K [1 ]
机构
[1] Sophia Univ, Fac Sci & Technol, Dept Chem, Chiyoda Ku, Tokyo 1028554, Japan
关键词
acid sites; Fe-ZSM-5; ion-exchange level; propene adsorption; selective catalytic reduction of N2O;
D O I
10.1016/S1387-1811(99)00223-1
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The direct decomposition and selective reduction of nitrous oxide (N2O) over Fe-ZSM-5 have been investigated in the presence of oxygen, using propene (C3H6) as reductant. The results are compared with those obtained over Cu-ZSM-5, which is known to possess very high activity for direct decomposition. When propene was added as reductant, the activity of Fe-ZSM-5 dramatically increased compared with the direct decomposition of N2O, whereas Cu-ZSM-5 was strongly deactivated. Some Fe-ZSM-5 catalysts having different ion-exchange levels have been prepared in order to investigate the effect of Fe ion on the selective reduction of N2O. The conversion of N2O to N-2 and the reactivity of absorbed C3H6 with N2O were increased with increased ion-exchange level. The activity over Fe-ZSM-5 lion-exchange level=81%) after calcination at 1073 K was found to be slightly higher than that at 773 K. Moreover, the observation of FT-IR spectroscopy after adsorption of C3H6 or pyridine on the catalyst showed that most of the Bronsted sites after calcination at 1073 K had disappeared. The results suggest that this reaction occurs mainly on Leu is acidic sites generated after the ion-exchange. (C) 2000 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:227 / 234
页数:8
相关论文
共 15 条
[11]  
SEGAWA K, 1994, T MRS JAP, V15, P131
[13]   Selective catalytic reduction of N2O by C3H6 over Fe-ZSM-5 [J].
Yamada, K ;
Pophal, C ;
Segawa, K .
MICROPOROUS AND MESOPOROUS MATERIALS, 1998, 21 (4-6) :549-555
[14]   Catalytic decomposition of N2O over supported rhodium catalysts: high activities of Rh/USY and Rh/Al2O3 and the effect of Rh precursors [J].
Yuzaki, K ;
Yarimizu, T ;
Ito, S ;
Kunimori, K .
CATALYSIS LETTERS, 1997, 47 (3-4) :173-175
[15]  
APPL CATAL B-ENVIRON