An environmentally friendly wide temperature CeWTiOx catalyst with superior performance for the selective catalytic reduction NOx with NH3

被引:45
|
作者
Huang Xiaosheng [1 ,2 ]
Zhang Guodong [1 ]
Dong Fang [1 ]
Tang Zhicheng [1 ]
机构
[1] Chinese Acad Sci, Lanzhou Inst Chem Phys, Natl Engn Res Ctr Fine Petrochem Intermediates, State Key Lab Oxo Synth & Select Oxidat, Lanzhou 730000, Gansu, Peoples R China
[2] Univ Chinese Acad Sci, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
Solvothermal synthesis; SCR performance; High dispersion; Large surface area; Synergistic effect; MIXED-OXIDE CATALYST; CE-W-TI; SURFACE CHARACTERIZATION; SOLVOTHERMAL SYNTHESIS; CEO2-WO3; CATALYSTS; CARBON NANOTUBES; CERIA; CEO2/TIO2; REDOX; STATE;
D O I
10.1016/j.jiec.2018.09.006
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A promising CeWTiOx catalyst for selective catalytic reduction of NOx with NH3 had been prepared by a facile one-pot solvothermal method, and the NO conversion could reach to 84% at 180 degrees C and maintain above 92% at the temperature range 200-460 degrees C. According to the NH3-TPD and N-2 adsorption-desorption, surface acidity and surface area (229.44 m(2)/g) of the catalysts were enhanced significantly, both of them were beneficial to the NH3 adsorption in the SCR process. Besides, the results of XRD, XPS, Raman spectra and TEM indicated that the high dispersion of cerium active species as well as tungsten on anatase TiO2 was also indispensably for the excellent SCR performance. Combined with the strong reduction capacity from H-2-TPR analysis as well as the enrichment of oxygen vacancy, it deserved the fine catalytic ability. More importantly, the strong synergistic effect between the Ce-W-Ti formed in the solvothermal system enhanced the catalyst's resistance to H2O and SO2. Thus the solvothermal synthesis showed an attractive perspective in the preparation of metal oxides catalysts for the SCR process. (C) 2018 The Korean Society of Industrial and Engineering Chemistry. Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:66 / 76
页数:11
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