Catalytic behaviors of CuO supported on Mn2O3 modified γ-Al2O3 for NO reduction by CO

被引:59
|
作者
Wan, Haiqin [1 ]
Li, Dan [2 ]
Dai, Yue [2 ]
Hu, Yuhai [2 ]
Liu, Bin [2 ]
Dong, Lin [2 ]
机构
[1] Nanjing Univ, Sch Environm, State Key Lab Pollut Control & Resource Reuse, Nanjing 210093, Jiangsu, Peoples R China
[2] Nanjing Univ, Sch Chem & Chem Engn, Key Lab Mesoscop Chem MOE, Nanjing 210093, Jiangsu, Peoples R China
基金
中国国家自然科学基金;
关键词
CuO/gamma-Al2O3; Manganese oxide; Modification; Dispersion capacity; Epitaxial growth; In situ IR; NO; CO; MANGANESE OXIDE CATALYSTS; RAY PHOTOELECTRON-SPECTROSCOPY; SITU FT-IR; CARBON-MONOXIDE; COPPER-OXIDE; CUO/GAMMA-AL2O3; CATALYSTS; SURFACE INTERACTIONS; ADSORPTION BEHAVIOR; SELECTIVE REDUCTION; OXIDATION;
D O I
10.1016/j.molcata.2010.08.016
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
CuO supported on gamma-Al2O3 and Mn2O3 modified gamma-Al2O3 was prepared and characterized by XRD, UV-vis, XPS,TPR and in situ adsorption IR. NO reduction by CO over these catalysts was also investigated. For the modification of gamma-Al2O3 by Mn2O3, manganese oxide was highly dispersed on gamma-Al2O3 surface to form a monolayer with a dispersion capacity of about 1.0 mmol Mn3+/100 m(2) gamma-Al2O3 corresponding to 8.1 wt.% of Mn. For supported copper oxide, CuO dispersion capacity was 0.75 mmol Cu2+/100 m(2) gamma-Al2O3 on gamma-Al2O3. and increased to 1.1 mmol Cu2+/100 m(2) gamma-Al2O3 on 1.0 MnOx-gamma-Al2O3, indicative of an elevated CuO dispersion capacity upon Mn2O3 modification. For NO reduction by CO, the addition of manganese oxide generally enhanced NO conversion and N-2 selectivity. Furthermore, the catalyst with the loading amounts of Cu and Mn of 0.6 mmol and 0.3/100 m(2) gamma-Al2O3 respectively exhibited the most prominent catalytic efficiency among the tested catalysts in terms of NO conversion and N-2 selectivity. Additionally, these catalysts showed stable NO conversion and N-2 selectivity. (C) 2010 Elsevier B.V. All rights reserved.
引用
收藏
页码:32 / 44
页数:13
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