Preparation, characterization, and catalytic performance of high efficient CeO2-MnOx-Al2O3 catalysts for NO elimination

被引:42
作者
Yao, Xiaojiang [1 ]
Li, Lulu [2 ,3 ]
Zou, Weixin [2 ,3 ]
Yu, Shuohan [2 ,3 ]
An, Jibin [4 ]
Li, Hongli [1 ]
Yang, Fumo [1 ]
Dong, Lin [2 ,3 ]
机构
[1] Chinese Acad Sci, Chongqing Inst Green & Intelligent Technol, Key Lab Reservoir Aquat Environm CAS, Chongqing 400714, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210093, Jiangsu, Peoples R China
[3] Nanjing Univ, Ctr Modern Anal, Jiangsu Key Lab Vehicle Emiss Control, Nanjing 210093, Jiangsu, Peoples R China
[4] Chongqing Univ Arts & Sci, Chongqing Key Lab Environm Mat & Remediat Technol, Chongqing 402160, Peoples R China
基金
中国国家自然科学基金;
关键词
Ceria-based mixed oxide; Incorporation; Electron interaction; Adsorption property; NO elimination; PLUS CO REACTION; LOW-TEMPERATURE; MIXED OXIDES; PHYSICOCHEMICAL PROPERTIES; CUO-CEO2; CATALYSTS; RAMAN-SPECTROSCOPY; SURFACE-AREA; REDUCTION; OXIDATION; CERIA;
D O I
10.1016/S1872-2067(15)61098-1
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A series of CeO2-MnOx-Al2O3 mixed oxide catalysts (Ce:Mn:Al mole ratio = 6:4:x, x = 0.25, 0.5, 1, 2) were prepared by a simple one-step inverse co-precipitation method to investigate the influence of the incorporation of Al3+ into CeO2-MnOx mixed oxides. CeO2-MnOx CeO2-Al2O3, and MnOxAl2O3 mixed oxides, and CeO2 were prepared by the same method for comparison. The samples were characterized by XRD, Raman, N-2 physisorption, H-2-TPR, XPS, and in situ DRIFTS. The catalytic re duction of NO by CO was chosen as a model reaction to evaluate the catalytic performance. The incorporation of a small amount of Al3+ into CeO2-Mna, mixed oxides resulted in a decrease of crystallite size, with the increase of the BET specific surface area and pore volume, as well as the in crease of Ce3+ and Mn4+. The former benefits good contact between catalyst and reactants, and the latter promotes the adsorption of CO and the desorption, conversion and dissociation of adsorbed NO. All these enhanced the catalytic performance for the NO+CO model reaction. A reaction mechanism was proposed to explain the excellent catalytic performance of CeO2-MnOx-Al2O3 catalysts for NO reduction by CO. (C) 2016, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:1369 / 1380
页数:12
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