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通过阴极还原和电芬顿法处理硝基酚。

Treatment of nitrophenols by cathode reduction and electro-Fenton methods.

作者信息

Yuan Songhu, Tian Meng, Cui Yanping, Lin Li, Lu Xiaohua

机构信息

Environmental Science Research Institute, Huazhong University of Science and Technology, Wuhan, Hubei 430074, PR China.

出版信息

J Hazard Mater. 2006 Sep 1;137(1):573-80. doi: 10.1016/j.jhazmat.2006.02.069. Epub 2006 May 2.

DOI:10.1016/j.jhazmat.2006.02.069
PMID:16650528
Abstract

This study deals with the degradation of various nitrophenols by cathode reduction and electro-Fenton methods. Phenols (Poh), 2-nitrophenol (2-NP), 3-nitrophenol (3-NP), 4-nitrophenol (4-NP), and 2,4-dinitrophenol (2,4-DNP) are treated and different degradation sequences are obtained. The relationship between the structure and activities of nitrophenols is discussed. Using 4-NP as a model nitrophenol, the electrochemical behaviors on graphite cathode and Pt anode are analyzed by cyclic voltammetry. The contribution of different reactions to the degradation of 4-NP is investigated in divided cells. The degradation of 4-NP is much faster in the cathode cell than in the anodic cell. In the cathode cell, the degradation of 4-NP is significantly enhanced by the introduction of aeration and Fe(2+). Ultraviolet-visible (UV-vis) spectra reveal different reaction pathways for the degradation in the anodic cell and cathode cell. Treatment of high concentration of 4-NP in the undivided cell shows that more than 98% removal of 4-NP and about 13% removal of total organic carbon (TOC) are obtained for both processes, while the subsequent biodegradability test shows that electro-Fenton can eliminate the toxicity and improve the biodegradability of 4-NP. Negligible quantity of nitrate and nitrite ions detected in both processes indicates that there is no direct release of -NO(2) and -NO groups from 4-NP and its degradation intermediates. Intermediates such as hydroquinone and bezoquinone are detected by gas chromatography/mass spectrum (GC/MS). The degradation pathway of 4-NP in electro-Fenton process is proposed as the cathode reduction followed by hydroxyl oxidation.

摘要

本研究探讨了通过阴极还原和电芬顿法降解各种硝基酚的情况。对苯酚(Poh)、2-硝基酚(2-NP)、3-硝基酚(3-NP)、4-硝基酚(4-NP)和2,4-二硝基酚(2,4-DNP)进行了处理,并获得了不同的降解顺序。讨论了硝基酚的结构与活性之间的关系。以4-NP作为模型硝基酚,通过循环伏安法分析了其在石墨阴极和铂阳极上的电化学行为。在分隔式电解槽中研究了不同反应对4-NP降解的贡献。4-NP在阴极槽中的降解速度比在阳极槽中快得多。在阴极槽中,曝气和Fe(2+)的引入显著增强了4-NP的降解。紫外可见(UV-vis)光谱揭示了阳极槽和阴极槽中降解的不同反应途径。在未分隔的电解槽中处理高浓度的4-NP表明,两种方法对4-NP的去除率均超过98%,对总有机碳(TOC)的去除率约为13%,而随后的生物降解性测试表明,电芬顿法可以消除4-NP的毒性并提高其生物降解性。在两个过程中检测到的硝酸盐和亚硝酸盐离子数量可忽略不计,这表明4-NP及其降解中间体没有直接释放出-NO(2)和-NO基团。通过气相色谱/质谱(GC/MS)检测到了对苯二酚和苯醌等中间体。提出了电芬顿法中4-NP的降解途径为阴极还原后羟基氧化。

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