催化作用
路易斯酸
化学
无机化学
布朗斯特德-洛瑞酸碱理论
硫黄
石墨烯
氧化物
脱氢
选择性催化还原
硫酸化
吸附
热液循环
化学工程
材料科学
纳米技术
有机化学
工程类
生物化学
作者
Qi Han,Shuangling Jin,Jitong Wang,Jiangcan Wang,Peng Sun,Yongbo Zhou,Xiaorui Wang,Rui Zhang,Wenming Qiao,Licheng Ling,Jin Mu
标识
DOI:10.1016/j.jpcs.2022.110782
摘要
The MnOx-CeOy/rGO catalysts were prepared by a facile hydrothermal method for selective catalytic reduction (SCR) of NO with NH3. Compared with MnOx-CeOy catalyst, the optimal MnOx-CeOy/rGO(0.1) catalyst not only shows an excellent low-temperature catalytic activity (60–180 °C), but also exhibits a better sulfur-resistant performance in the presence of 100 ppm SO2+5 vol% H2O at 160 °C. The in-situ DRIFTS results show that more NH4+ on Brønsted acid sites and NH3 on Lewis acid sites, as well as NH4HSO4 are detected on MnOx-CeOy catalyst during SCR reaction with SO2, while the adsorbed NHx species over MnOx-CeOy/rGO(0.1) catalyst can be quickly activated and consumed via Eley-Rideal (E-R) reaction pathway. The highly dispersed Ce sites can effectively protect more Mn active sites from sulfation, and the Mn sites with stronger acidity and abundant oxygen vacancy defects promote the oxidative dehydrogenation of NH3 to form NH2, thus enhancing the sulfur resistance of MnOx-CeOy/rGO(0.1) catalyst.
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