氮氧化物
选择性催化还原
催化作用
氧化还原
化学
路易斯酸
氧化物
亚硝酸盐
无机化学
砷
氨
核化学
X射线光电子能谱
化学工程
吸附
硝酸盐
有机化学
燃烧
工程类
作者
Xiang Li,Xiansheng Li,Junhua Li,Jiming Hao
标识
DOI:10.1016/j.jhazmat.2016.07.058
摘要
Arsenic resistance on MoO3 doped CeO2/TiO2 catalysts for selective catalytic reduction of NOx with NH3 (NH3-SCR) is investigated. It is found that the activity loss of CeO2-MoO3/TiO2 caused by As oxide is obvious less than that of CeO2/TiO2 catalysts. The fresh and poisoned catalysts are compared and analyzed using XRD, Raman, XPS, H2-TPR and in situ DRIFTS. The results manifest that the introduction of arsenic oxide to CeO2/TiO2 catalyst not only weakens BET surface area, surface acid sites and adsorbed NOx species, but also destroy the redox circle of Ce4+ to Ce3+ because of interaction between Ce and As. When MoO3 is added into CeO2/TiO2 system, the main SCR reaction path are found to be changed from the reaction between coordinated NH3 and ad-NOx species to that between an amide and gaseous NO. Additionally, for CeO2-MoO3/TiO2 catalyst, As toxic effect on active sites CeO2 can be released because of stronger As-Mo interaction. Moreover, not only are the reactable Brønsted and Lewis acid sites partly restored, but the cycle of Ce4+ to Ce3+ can also be free to some extent.
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