Tungsten modified MnOx-CeO2/ZrO2 monolith catalysts for selective catalytic reduction of NOx with ammonia

被引:123
作者
Xu, Haidi [1 ]
Zhang, Qiulin [1 ]
Qiu, Chuntian [1 ]
Lin, Tao [1 ]
Gong, Maochu [1 ]
Chen, Yaoqiang [1 ]
机构
[1] Sichuan Univ, Coll Chem, Minist Educ, Key Lab Green Chem & Technol, Chengdu 610064, Peoples R China
基金
中国国家自然科学基金;
关键词
NH3-selective catalytic reduction; Monolith catalyst; Catalyst activation; Environment; Pollution; Stability; LOW-TEMPERATURE SCR; OXIDE CATALYSTS; NITRIC-OXIDE; SURFACE-CHEMISTRY; MN/TIO2; CATALYST; MANGANESE OXIDES; NH3; CE; PERFORMANCE; RESISTANCE;
D O I
10.1016/j.ces.2012.04.012
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
A series of WO3-ZrO2 carriers were prepared by co-precipitation method with different mass fractions (0 wt%, 5 wt%, 10 wt%, 15 wt% and 20 wt%) of WO3, and MnOx-CeO2/WO3-ZrO2 monolith catalysts were prepared for selective catalytic reduction of NOx with ammonia (NH3-SCR) in the presence of excessive O-2. The catalysts were characterized by N-2 adsorption-desorption, X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and NH3/NO temperature-programmed desorption (NH3/NO-TPD). The experimental results showed that, the tungsten modified monolith catalyst MnOx-CeO2/WO3-ZrO2 with the WO3 content 10 wt% had the best catalytic activity and the widest reaction window; it possessed a better thermal stability than V2O5/WO3/TiO2 catalyst, and showed a better H2O and SO2 tolerance than MnOx-CeO2/ZrO2. The characterization results indicated that MnOx-CeO2/10% WO3-ZrO2 had the best textural properties, a well-dispersed state of WO3, the lowest binding energy of Ce3+ 3d(5/2), the maximum value of Ce3+:Ce=20.7%, the suitable molar ratio of Mn:Ce approximate to 1, and a co-existence state of MnO2-Mn2O3. In addition, it had the most adsorbed sites of NH3 or NO species. The NOx conversion was more than 80% in the temperature range of 150 degrees C to 380 degrees C at the space velocity of 10,000 h(-1). It possessed better potential for practical application. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:120 / 128
页数:9
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