催化作用
氮氧化物
吸附
化学
选择性
X射线光电子能谱
选择性催化还原
无机化学
氧化还原
大气温度范围
氧气
化学工程
物理化学
有机化学
燃烧
气象学
工程类
物理
作者
Mingming Wang,Shan Ren,Xiangdong Xing,Yuhan Zhou,Jie Yang,Lin Chen,Xiaodi Li
标识
DOI:10.1016/j.joei.2022.05.011
摘要
CeO2-NPs and α-MnO2 were prepared separately by hydrothermal method. Then the CeO2-NPs and α-MnO2 were mixed by impregnation method to prepare Mn4CeOx and MnCe4Ox catalysts for investigating their SCR catalytic performance. The results indicated that Mn4CeOx catalyst had a higher catalytic activity at 75–250 °C than that of MnCe4Ox catalyst, and the NOx conversion rate of Mn4CeOx catalyst reached the highest point at 150 °C, which was nearly 100%. Besides, N2 selectivity of Mn4CeOx catalyst was always slightly higher than that of MnCe4Ox catalyst in the testing temperature range. H2-TPR results showed that the redox ability of Mn4CeOx catalyst was higher than MnCe4Ox, which favored the SCR reaction. Meanwhile, NH3-TPD analysis revealed that Mn4CeOx catalyst had higher adsorption peak temperature and stronger surface acidity than that of MnCe4Ox catalyst, which effectively promoted the NH3 adsorption and activation. From XPS results, the relative content of Ce4+ in Mn4CeOx catalyst was 83.2%, which was higher than that of MnCe4Ox catalyst, indicating that Mn4CeOx catalyst could generate more Mn4+, and thus produce more oxygen vacancies, which promoted the SCR reaction. Finally, a reaction mechanism model for low-temperature SCR over MnCe4Ox and Mn4CeOx catalysts was proposed.
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