催化作用
X射线光电子能谱
价(化学)
化学
催化氧化
氧化还原
解吸
兴奋剂
氧化态
程序升温还原
无机化学
锰
氧化法
物理化学
材料科学
化学工程
吸附
有机化学
光电子学
工程类
作者
Wenbo Jia,Ying Li,Hao Chang,Songtao Liu,Yue Cao,Chuanmin Chen
出处
期刊:Energy & Fuels
[American Chemical Society]
日期:2023-09-06
卷期号:37 (18): 14202-14212
被引量:1
标识
DOI:10.1021/acs.energyfuels.3c02540
摘要
A series of Mn-doped VWTi (Mn-VWTi) catalysts were prepared and used for simultaneous NO removal and Hg0 oxidation at a wide temperature window of 200–400 °C for the first time, and the catalytic activity of the Mn-VWTi catalysts was investigated. The results indicated that Mn doping could notably improve the NO removal activity at 200–300 °C and the Hg0 oxidation activity at 200–400 °C, and the catalyst with 3% Mn loading exhibited superior catalytic activity. The relationship between NO removal and Hg0 oxidation and the effects of NO and NH3 concentrations on Hg0 oxidation over a Mn3-VWTi catalyst were also explored to verify the possibility of synergistic NO removal and Hg0 oxidation on a Mn-VWTi catalyst at a wide temperature window of 200–400 °C. In addition, several characterization methods, including Brunauer–Emmett–Teller, X-ray diffraction, H2 temperature-programmed reduction, X-ray photoelectron spectroscopy, and Hg temperature-programmed desorption, were used to characterize the catalyst, and the Hg0 oxidation mechanism over the Mn3-VWTi catalyst was also investigated based on the experimental data and characterization results. It was revealed that Mn species with higher valence states (Mn4+/Mn3+) played a major role during the Hg0 oxidation process at the lower temperature of 250 °C, while the synergistic interaction between Mn and V species (Mn4+/Mn3+ + V4+ ↔ Mn2+ + V5+) showed a dominant role in Hg0 oxidation at the higher temperature of 350 °C. Moreover, the oxidized mercury species mainly existed in the form of HgO on the catalyst surface.
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