姜楠

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副教授

博士生导师

硕士生导师

性别:女

毕业院校:大连理工大学

学位:博士

所在单位:电气工程学院

学科:电工理论与新技术. 环境工程. 高电压与绝缘技术

办公地点:静电与特种电源研究所303

联系方式:jiangnan@dlut.edu.cn

电子邮箱:jiangnan@dlut.edu.cn

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Synergetic effect of TiO2 and Fe3+ as co-catalysts for enhanced phenol degradation in pulsed discharge system

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论文类型:期刊论文

发表时间:2018-02-01

发表刊物:APPLIED CATALYSIS B-ENVIRONMENTAL

收录刊物:SCIE、EI

卷号:221

页面范围:521-529

ISSN号:0926-3373

关键字:Pulsed discharge plasma; TiO2; Fe3+; Synergetic effect; Phenol decomposition

摘要:In this work, the synergetic effect of TiO2 and Fe3+ in pulsed discharge plasma has systematically investigated using phenol as the probe molecule. The dominant effects of TiO2 and Fe3+ dosage were firstly studied, and then phenol degradation was investigated in four parallel experiments including plasma alone, plasma/Fe3+, plasma/TiO2 and plasma/Fe3+/TiO2. The experimental results showed that the phenol removal efficiency in plasma/Fe3+/TiO2 system increased by 25% in comparison with plasma alone, which were only 9% and 10% in plasma/TiO2 and plasma/Fe3+ system, indicating a significantly synergistic effect between Fe3+ and TiO2. To illustrate the synergetic effect of TiO2 and Fe3+ ions, the TiO2 structural characterization was analyzed by XPS, UV-vis spectra and XRD, and Fe2+ and center dot OH concentration was also determined during discharge process. The Fe3+ ions and excited nitrogen from plasma discharge were doped on TiO2 particles, which narrowed the band gap of TiO2 from 3.0 eV to 2.0 eV and enlarged the absorption edge at around 600 nm, and therefore enhanced the photocatalytic activity in the visible light. The co-doping of Fe3+ and nitrogen significantly increased the separation rate of photo-generated electrons and holes and prolonged their lifetime. The photoelectron-transfer pathway was blocked by Fe3+, the Fe3+ ions could be changed to Fe2+ ions using photoelectron on TiO2 surface, inducing Fenton-like reaction for the enhancement of the center dot OH formation rate in the plasma/TiO2/Fe3+ system. The concentration of center dot OH increased from 14.8 x 10(-5) mol L-1 in the plasma/TiO2 system to 20.6 x 10(-5) mol L-1 in the plasma/TiO2/Fe3+ system.