催化作用
氮氧化物
化学
选择性催化还原
Keggin构造
选择性
无机化学
X射线光电子能谱
化学工程
物理化学
有机化学
燃烧
工程类
作者
Yun Geng,Kai Jin,Jian Mei,Guanyong Su,Lei Ma,Shijian Yang
标识
DOI:10.1016/j.jhazmat.2019.121032
摘要
The CeO2 catalysts grafted with heteropoly acid (i.e., HPA) could enhance their catalytic performance for selective catalytic reduction of NOx with NH3 (NH3-SCR). In comparison to HSiW/CeO2, HPMo/CeO2, and commercial V2O5-WO3/TiOx catalysts, HPW/CeO2 catalysts showed the best SCR performance. XPS and DRIFTS demonstrated that the amount of HPA on HPW/CeO2 was more than those on HSiW/CeO2 and HPMo/CeO2. H2-TPR results indicated that reducibility of HPMo/CeO2 was stronger than those of HSiW/CeO2 and HPW/CeO2, resulting in the high-temperature performance loss. According to kinetic results, below 250 °C, kSCR-ER and kSCR-LH of HPW/CeO2 were higher than those of HSiW/CeO2, meanwhile kside of both HSiW/CeO2 and HPW/CeO2 were low. Therefore, HPW/CeO2 had the better SCR performance than HSiW/CeO2. As NH3 was completely consumed, SCR activity depended on the ratio of SCR reaction in the consumption of NH3. The selectivity of SCR reaction, NSCR reaction, and C-O reaction of HSiW/CeO2 were almost the same as those of HPW/CeO2 above 250 °C, resulting in the NOx conversion of HPW/CeO2 was basically the same as that of HSiW/CeO2 above 250 °C. Due to the lowest kSCR-ER and kSCR-LH, and highest kside, NOx conversion of HPMo/CeO2 was the worst compared to HSiW/CeO2 and HPW/CeO2 catalysts.
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