催化作用
选择性催化还原
铈
吸附
X射线光电子能谱
硫酸化
金属
无机化学
化学
硫酸盐
氧化还原
化学工程
材料科学
物理化学
有机化学
生物化学
工程类
作者
Lei Zhang,Lulu Li,Yuan Cao,Xiaojiang Yao,Chengyan Ge,Fei Gao,Yu Deng,Changjin Tang,Lin Dong
标识
DOI:10.1016/j.apcatb.2014.10.029
摘要
A series of inverse TiO2/CeO2 catalysts were prepared by the impregnation method and their catalytic performances for the selective catalytic reduction of NO by NH3 have been tested with and without SO2 and/or H2O. Compared with the normally discussed CeO2/TiO2 catalyst, the advantage of inverse TiO2/CeO2 catalyst was not only shown a good low temperature catalytic activity (150–250 °C), but also exhibited much better SO2 resistance performances with the existence of 200 ppm SO2 and/or 5 vol.% H2O at 300 °C. Furthermore, SO2 had more significant inhibitory effect on catalytic activity than H2O based on the configuration differences of Ce–Ti-based catalysts. These catalysts were investigated by means of TG-DTA, XRD, BET, in situ DRIFT, XPS and H2-TPR. The results demonstrated that the sulfation of these samples under reactive conditions mainly generated three different kinds of sulfate species including NH4HSO4, surface and bulk-like metal sulfates (mainly interacted with cerium species). The formed metal sulfates blocked the active sites of Ce–O–Ti and resulted in the deactivation of CeO2/TiO2. Although metal sulfates were also formed over TiO2/CeO2, NH3-SCR could still proceed and that was similar as the reaction system with the use of sulfated CeO2 as the catalyst. Meanwhile, the interactions between SO2 and Ce–Ti-based catalysts were discussed in detail and an adsorption model of SO2 was proposed.
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