介孔材料
氧化剂
催化作用
铈
氮氧化物
X射线光电子能谱
烟气
氧化态
过渡金属
无机化学
材料科学
选择性催化还原
兴奋剂
化学工程
化学
燃烧
有机化学
光电子学
工程类
作者
Chun-Nan Kuo,Kwang‐Hwa Lii,Yu-Lun Lai,S.-J. Yen
出处
期刊:Catalysts
[Multidisciplinary Digital Publishing Institute]
日期:2023-04-03
卷期号:13 (4): 694-694
被引量:5
标识
DOI:10.3390/catal13040694
摘要
Selective catalytic reduction (SCR) is an effective system for treating nitrogen oxides (NOx; mainly NO), and fast SCR requires the equimolar reactants of NO and NO2. This study focused on catalysts for oxidizing 50% of NO to NO2. A series of catalysts composed of a variety of components, such as mesoporous mMnO2-nCeO2 as carrier catalysts (m:n = 9:1 and 7:3) and transition metals (e.g., Fe, Co, Ni, Cu, and Cr), were synthesized and characterized using N2 adsorption, in situ XRD, TEM, and XPS. All samples had a mesoporous structure with pore size around 8 nm. XPS results demonstrated that addition of cerium ion increased the surface area and provided oxygen vacancy due to the formation of Ce3+ within the structure. NO oxidation activity was tested using a feed (205~300 ppm NO and 6% O2) that simulated typical flue gas conditions. Doped mesoporous mMnO2–nCeO2 has higher NO oxidation activity than pristine mMnO2–nCeO2. The doped mMnO2-nCeO2 catalyzed 50% of NO to NO2 at between 140 and 200 °C resulting in an equivalent amount of NO and NO2. Among the transition metals, Cu, Ni, Co, Fe, and Cr have the highest to lowest oxidation activity, respectively. The precatalytic oxidation of NO can potentially be combined with the current SCR system without changes to existing equipment and can be applied to the exhaust gas treatment for de-NOx.
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