个人信息Personal Information
教授
博士生导师
硕士生导师
性别:男
毕业院校:大连理工大学
学位:博士
所在单位:物理学院
学科:等离子体物理
电子邮箱:amzhu@dlut.edu.cn
A combined DRIFTS and MS study on reaction mechanism of NO reduction by CO over NiO/CeO2 catalyst
点击次数:
论文类型:期刊论文
发表时间:2009-08-17
发表刊物:APPLIED CATALYSIS B-ENVIRONMENTAL
收录刊物:SCIE、EI
卷号:90
期号:3-4
页面范围:395-404
ISSN号:0926-3373
关键字:NiO/CeO2 catalyst; NO-CO; NCO complexes; DRIFTS; MS
摘要:Previously, we reported the prominent catalytic activity of ceria-supported nickel oxide catalyst for the reduction of NO by CO [Y. Wang, A.M. Zhu, Y.Z. Zhang, C.T. Au, X.F. Yang, C. Shi, Appl. Catal. B 81 (2008) 141-149]. In the present study, the reaction mechanism of NO and CO over the NiO/CeO2 catalyst has been examined in two kinds of reaction modes: (i) NO reaction with CO pre-treated catalyst and (ii) CO reaction with NO pre-treated catalyst, by employing in situ diffuse reflectance infrared Fourier transform spectroscopy (DRIFTS) coupled with mass spectroscopy (MS) techniques. It was found that the generation of surface NCO complexes and N-2 (9) Occurs only in mode (i), which gives obvious evidence of NO dissociation over CO pre-reduced NiO/CeO2 Catalyst. The result is similar to that obtained in the case of NO and CO co-adsorption, but different from that of mode (ii). The overall results indicate that CO reduction of surface oxygen should be the first and crucial step, and the dissociation of NO on the CO-reduced surface is a pathway for N-2 generation. The other pathway for N-2 generation is the interaction of NCO complexes with NO. Based on these understandings, we proposed reaction steps for the catalytic reduction of NO by CO over the NiO/CeO2 catalyst. (C) 2009 Elsevier B.V. All rights reserved.