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张晖实验室博士生严素定的论文在CHEMICAL ENGINEERING JOURNAL 刊出
发布时间:2019-02-15 15:40:41     发布者:易真     浏览次数:

标题:Enhanced persulfate-mediated photocatalytic oxidation of bisphenol A using bioelectricity and a g-C3N4/Fe2O3 heterojunction

作者: Yan, SD (Yan, Suding); Shi, Y (Shi, Yue); Tao, YF (Tao, Yufang); Zhang, H (Zhang, Hui)

来源出版物:CHEMICAL ENGINEERING JOURNAL  卷: 359  页码: 933-943  DOI 10.1016/j.cej.2018.11.093 出版年: MAR 1 2019  

摘要: Photocatalysis and sulfate radical based advanced oxidation processes have gained considerable popularity in the field of contaminant degradation. However, there are few reports focusing on the combination of these two promising technologies, especially the coupling of a visible light responsive catalyst with an electro-assisted persulfate activation system. Herein, a traditional g-C3N4/Fe2O3 (CNFe) heterojunction was prepared by a facile one-pot calcination and it could efficiently activate peroxydisulfate (PDS) for bisphenol A (BPA) decomposition with visible light and low-voltage bioelectricity supplied by a microbial fuel cell (MFC). The CNFe catalyst demonstrated good stability and could be reused at least five runs with negligible iron leaching. Sulfate and hydroxyl radicals and singlet oxygen were responsible for the BPA degradation. A mechanism for BPA destruction in the studied system is proposed based on the results of electron paramagnetic resonance (EPR), trapping experiments, X-ray photoelectron spectroscopy (XPS) and the band edge potential of g-C3N4 and Fe2O3. The effects of reaction conditions on the BPA oxidation were explored and 92.2% of BPA was removed after 60 min reaction using 10 mM of PDS, 0.5 g L-1 of CNFe, 100 mA m(-2) of current density and natural pH. The total organic carbon (TOC) removal was only 70.0%, but when the time was extended to 2 h, it rose to 91.0%, indicating high mineralization of the proposed system.

入藏号:WOS:000454137400091

文献类型:Article

语种:English

作者关键词: Peroxydisulfate activation; Photo-bioelectricity; g-C3N4/Fe2O3 heterojunction; Sulfate radical; Singlet oxygen

通讯作者地址:Zhang, H (reprint author), Wuhan Univ, Dept Environm Sci & Engn, POB C319,Luoyu Rd 129, Wuhan 430079, Hubei, Peoples R China.

电子邮件地址:eeng@whu.edu.cn

地址:

[Yan, Suding; Tao, Yufang; Zhang, Hui] Wuhan Univ, Dept Environm Sci & Engn, Hubei Environm Remediat Mat Engn Technol, Res Ctr, Wuhan 430079, Hubei, Peoples R China.
[Shi, Yue] Hubei Normal Univ, Dept Environm Engn, Hubei Key Lab Pollutant Anal & Reuse Technol, Huangshi 435002, Peoples R China.

影响因子:6.735

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