High calcium resistance of CeO2-WO3 SCR catalysts: Structure investigation and deactivation analysis

被引:89
作者
Li, Xiang [1 ]
Li, Xiansheng [1 ]
Li, Junhua [1 ]
Hao, Jiming [1 ]
机构
[1] Tsinghua Univ, Sch Environm, State Key Joint Lab Environm Simulat & Pollut Con, Beijing 100084, Peoples R China
基金
中国国家自然科学基金; 中国博士后科学基金;
关键词
NH3-SCR; Ca poisoned; Resistance; Adsorbed NO2; Acid sites; MIXED-OXIDE CATALYST; VANADIA-TITANIA CATALYSTS; ACTIVE-SITES; NITRIC-OXIDE; REGENERATION METHOD; NOX REDUCTION; NH3; MECHANISM; SURFACE; AMMONIA;
D O I
10.1016/j.cej.2017.02.027
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The SCR performances of CaO poisoning CeO2-WO3 and V2O5-WO3/TiO2 catalysts were prepared and compared for selective catalytic reduction of NO with NH3 (NH3-SCR). It was found that the CeO2-WO3 catalyst showed better calcium resistance than V2O5-WO3/TiO2 catalyst even when the CaO mass percentage reached up to 5 wt%. In order to further understand the resistance mechanism, XRD, Raman, XPS, H-2-TPR, NH3-TPD and in situ DRIFTS were used to analyze and explore the changes of CeO2-WO3 catalysts before and after the CaO deactivation. The results manifested that the introduction of Ca species not only affected CeO2 lattice but also led to CaWO4 formation on the surface. Additionally, although CaO increased the surface chemisorbed oxygen and Ce4+ species, the reducibility and Lewis acid sites, NH3 chemisorbed amount and Bronsted acid sites were greatly inhibited after deactivation. Furthermore, the enhanced NO2 adsorption capacity after the alkaline Ca species introduction could partially offset the negative effect in the loss of acid sites over the catalyst surface, which might be the primary reason for stronger CaO resistance of CW catalyst than traditional V2O5-WO3/TiO2 catalyst. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:70 / 79
页数:10
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