Reaction mechanism of elemental mercury oxidation to HgSO4 during SO2/SO3 conversion over V2O5/TiO2 catalyst

被引:30
作者
Yang, Yingju [1 ]
Liu, Jing [1 ]
Wang, Zhen [1 ]
Yu, Yingni [1 ]
机构
[1] Huazhong Univ Sci & Technol, Sch Energy & Power Engn, State Key Lab Coal Combust, Wuhan 430074, Peoples R China
基金
中国博士后科学基金;
关键词
Reaction mechanism; Hg-0; oxidation; SO2/SO3; conversion; V2O5/TiO2; catalyst; HgSO4; formation;
D O I
10.1016/j.proci.2020.10.007
中图分类号
O414.1 [热力学];
学科分类号
摘要
Experiments and density functional theory calculations were conducted to uncover the reaction chemistry of Hg-0 oxidation during SO2/SO3 conversion over V2O5/TiO2 catalyst. The results show that SO2 promotes Hg-0 oxidation over V2O5/TiO2 catalyst with the assistance of oxygen. The promotional effect is dependent on the reaction temperature, and is associated with the bimolecular reaction between Hg-0 and SO3 over V2O5/TiO2 catalyst. SO2 can be oxidized to SO3 which has high oxidation ability for Hg-0 oxidation. SO2/SO3 conversion proceeds through a three-step reaction process in the sequence of SO2 adsorption -> SO2 oxida-tion -> SO3 desorption. SO2 oxidation presents an activation energy barrier of 223.84 kJ/mol. HgSO4 species is formed from the bimolecular reaction between Hg-0 and SO3 over V2O5/TiO2 catalyst. Hg-0 oxidation by SO3 over V2O5/TiO2 catalyst occurs through three reaction pathways, which are energetically favorable for HgSO4 formation. SO2* -> SO3* is identified as the rate-determining step of HgSO4 formation. During Hg-0 oxidation by SO3 over V2O5/TiO2 catalyst, HgSO4 desorption is a highly endothermic reaction process and requires a higher external energy. The proposed skeletal reaction network can be used to well understand the reaction mechanism of Hg-0 oxidation during SO2/SO3 conversion over V2O5/TiO2 catalyst. (C) 2020 The Combustion Institute. Published by Elsevier Inc. All rights reserved.
引用
收藏
页码:4317 / 4325
页数:9
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