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个人信息Personal Information
教授
博士生导师
硕士生导师
任职 : 精细化工全国重点实验室主任,教育部智能材料化工前沿科学中心执行主任,大连理工大学膜科学与技术研究开发中心主任
性别:女
毕业院校:中国科学院大连化物所
学位:博士
所在单位:化工学院
学科:化学工程. 膜科学与技术. 生物医学工程
联系方式:hgaohong@dlut.edu.cn
电子邮箱:hgaohong@dlut.edu.cn
Reaction mechanism for the influence of SO2 on Hg-0 adsorption and oxidation with Ce-0.1-Zr-MnO2
点击次数:
论文类型:期刊论文
发表时间:2017-09-01
发表刊物:FUEL
收录刊物:SCIE、EI、Scopus
卷号:203
页面范围:308-315
ISSN号:0016-2361
关键字:Element mercury removal; SO2 poisoning; Ce-0.1-Zr-Mn; Adsorption; Oxidation
摘要:The removal of Hg-0 from flue gas has been one of the primary challenges in the control of mercury emission. The presence of even small amounts of SO2 has a significant influence on the Hg-0 removal process, and the mechanism of this process has not been thoroughly explained to date. To understand the mechanism for SO2 influence, the influence of SO2 on the Hg0 adsorption and Hg-0 oxidation components of the Hg-0 removal process were investigated separately based on Ce-0.1-Zr-MnO2 center dot SO2 was shown to have serious negative effects on the Hg-0 adsorption process due to the reaction between SO2 and Mn-based active sites, as determined by TGA and XPS results. In contrast, for the Hg0 oxidation process Mn-SO42 formed through the reaction between SO2 and Mn-based active sites, and Mn-SO42 had a certain contribution to Hg-0 oxidation. Moreover, XPS results indicated that SO2 reacts with O-2 to form SO3 which adsorbed on the catalyst surface and act as new active sites, promoting Hg-0 oxidation via: Hg + SO3 + 1/2O(2) -> HgSO4. This phenomenon caused the catalyst to retain Hg-0 oxidation activity in the presence of SO2 for a relatively long time. (C) 2017 Elsevier Ltd. All rights reserved.