催化作用
结晶度
选择性催化还原
化学
选择性
X射线光电子能谱
反应性(心理学)
氮氧化物
硫化
热液循环
无机化学
反硝化
比表面积
核化学
化学工程
物理化学
有机化学
结晶学
氮气
燃烧
工程类
医学
替代医学
病理
作者
Bingbing Luo,Zhufeng Wang,Jiawei Huang,Shuying Ning,Wenyi Deng,Bingtao Zhao,Yaxin Su
标识
DOI:10.1016/j.jece.2023.109950
摘要
One-step hydrothermal synthesis method was used to prepare the Ho-doped OMS-2 catalyst (Hox-OMS-2) and the reactivity for selective catalytic reduction of NO with CO (CO-SCR) was examined. The outcomes demonstrated that the Ho0.05-OMS-2 catalyst displayed very attractive CO-SCR activity at 225 °C when the Ho/Mn molar ratio was 0.05, e.g., approximately 100% NO conversion and N2 selectivity. Furthermore, even in the presence of 0.02% SO2, the Ho0.05-OMS-2 catalyst can retain more than 80% NO conversion at 200–250 °C, and the catalyst has good sulfur resistance. SEM, XRD, BET, XPS, H2-TPR, and NH3-TPD were used to characterize the catalysts and analyze how the presence of Ho species in Hox-OMS-2 affected their physicochemical properties and reactivity. The outcomes show that the lattice expansion, decreased crystallinity, high specific surface area, increased Mn4+ concentration, enhanced surface oxygen vacancies and more Brønsted acidic bits can all contribute to the improved low-temperature activity of Hox-OMS-2 catalysts. Based on the In situ DRIFTS analysis, possible E-R mechanism (30–100 °C) and L-H mechanism (125–300 °C) of the catalysts were proposed.
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