Study on the direct decomposition of nitrous oxide over Fe-beta zeolites: From experiment to theory

被引:36
作者
Chen, Biaohua [1 ]
Liu, Ning [1 ]
Liu, Xingyong [1 ]
Zhang, Runduo [1 ]
Li, Yaping [1 ]
Li, Yingxia [1 ]
Sun, Xiuliang [1 ]
机构
[1] Beijing Univ Chem Technol, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
基金
中国国家自然科学基金; 高等学校博士学科点专项科研基金;
关键词
Nitrous oxide; BEA zeolite; DFT; Catalytic decomposition; Mechanism; SELECTIVE CATALYTIC-REDUCTION; N2O DECOMPOSITION; NITRIC-OXIDE; TRANSITION-METAL; ACTIVE-SITES; FE-ZSM-5; NO; OXYGEN; ADSORPTION; ACID;
D O I
10.1016/j.cattod.2011.04.010
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
N2O direct decomposition over Fe-beta zeolite prepared by wet ion-exchange (WIE) was systematically investigated based on the experimental and theoretical studies in this paper. Both isolated iron ions in the charge compensation positions and highly dispersed FeOx-like crystallite were verified by means of H-2-TPR. Catalytic performances of various Fe-BEA zeolites with diverse iron contents were thereafter studied. The results showed that: (1) the catalytic activity of bare beta zeolite was significantly promoted via ion-exchange; (2) no obvious further increase in deN(2)O activity was observed for Fe-beta samples with iron contents higher than 1%. Two kinds of reaction mechanism, with respective formation of oxygen (O-2) or nitrogen oxide (NOx) intermediate, for the direct decomposition of N2O over Fe-beta zeolite (noted as Fe-Z) were proposed according to the N2O-TPD, NO2-TPD, N-2-TPD, N2O-TPSR, and in situ DRIFTS investigation and density functional theory (DFT) study. The corresponding energy calculations for O-2-formation mechanism revealed that O-2 desorption was the rate determining step with an energy barrier of 63.20 kcal/mol. Another mechanism with NO formation was also simulated by DFT calculations, whose energy calculations indicated that the formation of Fe-Z-(NO)(2) was the main pathway for NO generation with an energy barrier of 26.92 kcal/mol. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:245 / 255
页数:11
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