贺高红

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

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Simultaneous removal of Hg-0 and NO from flue gas by Co-0.3-Ce-0.35-Zr0.35O2 impregnated with MnOx

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论文类型:期刊论文

发表时间:2017-10-15

发表刊物:CHEMICAL ENGINEERING JOURNAL

收录刊物:SCIE、EI、Scopus

卷号:326

页面范围:1210-1222

ISSN号:1385-8947

关键字:Simultaneous Hg-0 oxidation and NO; conversion; Element mercury; Nitrogen oxide; Mn-0.1/Co-0.3-Ce-0.35-Zr0.35O2

摘要:Hg-0 removal with SCR system can result in co-benefits of the apparatus, but the simultaneous removal efficiencies of Hg-0 and NO are not good enough and the mechanism of interaction between Hg-0 and SCR atmosphere has not been well known. In our previous work, Co-0.3-Ce-0.35-Zr0.35O2 has been proved to have an excellent Hg-0 oxidation efficiency. Therefore, in the present work, Co-0.3-Ce-0.35-Zr0.35O2 was used as a support to load SCR active component Mn and to obtain Mn-0.1/Co-0.3-Ce-0.35-Zr0.35O2 catalyst. Mn-0.1/Co-0.3-Ce-0.35-Zr0.35O2 showed excellent simultaneous efficiencies of Hg-0 oxidation (83.6%) and NO conversion (89.4%) at 180 degrees C under a high GHSV 180,000 h(-1). Furthermore, the interaction between Hg-0 and SCR atmosphere lowered the simultaneous efficiencies when compared to the separated ones. The decrease of Hg-0 oxidation efficiency in SCR + Hg-0 atmosphere was mainly attributed to the competitive adsorption between NH3 and Hg-0. Although NO and O-2 were beneficial for Hg-0 oxidation, it could not offset the inhibitive effect of NH3. Meanwhile, HgO accumulated on the catalyst surface resulted in occupation of active sites, which was responsible for the decrease of NO conversion in SCR + Hg-0 atmosphere. The individual gas components (H2O and SO2) showed negative effects on the simultaneous efficiencies of Hg-0 oxidation and NO conversion. (C) 2017 Elsevier B.V. All rights reserved.