Separate/simultaneous catalytic reduction of sulfur dioxide and/or nitric oxide by carbon monoxide over titanium-tin solid solution catalysts

被引:11
作者
Zhang, ZL [1 ]
Jun, M
Yang, XY
机构
[1] Peking Univ, Catalysis Div, Coll Chem & Mol Engn, Beijing 100081, Peoples R China
[2] Hainan Liuhe Environm Protect Catalysts Co Ltd, Haikou 570216, Peoples R China
关键词
SO2; NO; CO; catalytic reduction; tin dioxide; titania; solid solution;
D O I
10.1016/S1385-8947(03)00061-5
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Titanium-tin solid solutions prepared by coprecipitation were studied for the separate and simultaneous catalytic reduction of SO2 and/or NO by CO. Physicochemical characterizations of the solid solutions before and after reactions with different SnO2 contents were conducted to disclose the reaction mechanism by means of XRD, CO-TPR, XPS and transient MS techniques. It is found that TiO2-SnO2 solid solutions were very active towards the reduction of SO2 by CO at a low temperature and space velocity. There existed a strong synergistic promoted effect. which can be explained based on an enhanced redox mechanism proposed in the work. Furthermore, TiO2-SnO2 solid solutions would show a pronounced increase in catalytic activity during the reduction of NO by CO after the catalysts finished SO2 + CO reactions, or by introducing SO2 into the reaction feed. This promoting effort is due to the formation of tin sulfide species as a product of the reduction of SO2 by CO on the catalyst surface. A NO decomposition mechanism with the formation of SO2 by-product was proposed. The produced SO2 was in situ catalytically reduced to sulfur to regenerate tin sulfide. Lastly, simultaneous catalytic reduction of SO2 and NO using CO as a reducing agent was carried out on TiO2-SnO2 solid solution catalysts. Experimental results showed that at a temperature above 350 degreesC. SO2 and NO conversions are greater than 91 and 99%, respectively. (C) 2003 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:15 / 24
页数:10
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