催化作用
煅烧
吸附
纳米颗粒
大气温度范围
选择性催化还原
材料科学
锰
比表面积
氧化还原
化学工程
无机化学
化学
纳米技术
物理化学
有机化学
工程类
物理
气象学
作者
Fei Zhao,Guodong Zhang,Zhicheng Tang,Fei Zha
出处
期刊:Fuel
[Elsevier BV]
日期:2022-04-15
卷期号:322: 124185-124185
被引量:16
标识
DOI:10.1016/j.fuel.2022.124185
摘要
Mn-based catalysts had favorable low temperature SCR performance but it was restricted its practical application due to easy deactivation. Different proportions of Fe species were doped into Mn-MOFs as a precursor by a simple one-pot solvothermal method. A series of MnOx, Mn4FeOx, MnFeOx and MnFe4Ox catalysts with different structures were obtained by calcining under air. MnFeOx showed better catalytic activity and water resistance at low temperature. The NO conversion was 96% at 200 °C and kept above 85% in the range of 120–280 °C. Through a series of characterizations, it was found that manganese and iron species were highly dispersed in the MnFeOx catalyst, which was a vital factor for SCR reaction. Moreover, the MnFeOx catalyst not only possessed a large specific surface area and pore volume but also had a better reduction ability and abundant oxygen vacancies to adsorb and activate the reaction gases. Therefore, the catalyst possessed a satisfactory catalytic performance. More importantly, charging transfer between active manganese species and iron species in MnFeOx catalyst could effectively inhibit H2O poisoning and improve the stability of the catalyst. The results of in situ DRIFTs experiments showed that the low temperature NH3-SCR reaction of MnFeOx catalyst followed L-H mechanism. The effects of Fe doping content on the crystal structure of active species and SCR performance of manganese-based catalysts were revealed.
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