催化作用
掺杂剂
热稳定性
化学
硫黄
氧化还原
兴奋剂
吸附
无机化学
选择性催化还原
离子
化学工程
材料科学
有机化学
光电子学
工程类
作者
Huirong Li,Leonhard Schill,Qi Gao,Susanne Mossin,Anders Riisager
出处
期刊:Fuel
[Elsevier]
日期:2024-02-01
卷期号:358: 130111-130111
标识
DOI:10.1016/j.fuel.2023.130111
摘要
Fe-doped MnOx catalyst prepared by a preferred solvothermal method displayed noticeably better low-temperature (LT) NH3-SCR performance and water stability than an analogously prepared Al-doped MnOx catalyst. The SCR activity of both catalysts decreased markedly when exposed to SO2, but the resultant MnFeOx-S catalyst retained higher LT activity than MnAlOx-S and recovered significantly more of its original activity after thermal regeneration (400 °C). Comprehensive characterization confirmed that the deactivation of the catalysts was governed by formation of stable metal sulfates, which only decomposed to a minor extent upon thermal treatment although Al doping lowered the thermal stability of the adsorbed sulfur species. Additionally, Fe doping was found to facilitate electron transfer between Mn and Fe ions and weaken the interaction between active sites and deposited sulfates during the heating procedure, which promoted re-oxidation of Mn2+ to catalytically active Mn3+/Mn4+. Altogether, the altered redox properties resulted in improved LT SCR performance, enhanced water stability, higher SO2 tolerance and superior regeneration of the MnFeOx catalyst.
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