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微生物电解池系统阴极处理2-氯-4-硝基苯酚废水的性能与机理探究

刘靖 杨筱玲 罗萃 周中敏 梁一夫 郭勤 黄冬根

刘靖, 杨筱玲, 罗萃, 周中敏, 梁一夫, 郭勤, 黄冬根. 微生物电解池系统阴极处理2-氯-4-硝基苯酚废水的性能与机理探究[J]. 环境工程, 2026, 44(2): 40-49. doi: 10.13205/j.hjgc.202602005
引用本文: 刘靖, 杨筱玲, 罗萃, 周中敏, 梁一夫, 郭勤, 黄冬根. 微生物电解池系统阴极处理2-氯-4-硝基苯酚废水的性能与机理探究[J]. 环境工程, 2026, 44(2): 40-49. doi: 10.13205/j.hjgc.202602005
LIU Jing, YANG Xiaoling, LUO Cui, ZHOU Zhongmin, LIANG Yifu, GUO Qin, HUANG Donggen. Performance and mechanism of cathodic treatment of 2-chloro-4-nitrophenol contaminated wastewater in microbial electrolysis cells[J]. ENVIRONMENTAL ENGINEERING , 2026, 44(2): 40-49. doi: 10.13205/j.hjgc.202602005
Citation: LIU Jing, YANG Xiaoling, LUO Cui, ZHOU Zhongmin, LIANG Yifu, GUO Qin, HUANG Donggen. Performance and mechanism of cathodic treatment of 2-chloro-4-nitrophenol contaminated wastewater in microbial electrolysis cells[J]. ENVIRONMENTAL ENGINEERING , 2026, 44(2): 40-49. doi: 10.13205/j.hjgc.202602005

微生物电解池系统阴极处理2-氯-4-硝基苯酚废水的性能与机理探究

doi: 10.13205/j.hjgc.202602005
基金项目: 

国家自然科学基金项目“鼠李糖脂作用下氯硝柳胺在泥微生物电解系统迁移与共基质降解特性”(41967046);江西省交通设计研究院科技项目“基于短程硝化-MBR工艺的高速公路服务区中水回用系统应用”(院科技字[2023]9号)

详细信息
    作者简介:

    刘靖(2001—),男,硕士研究生,主要研究方向为水污染处理研究。1582367207@qq.com

    通讯作者:

    黄冬根(1964—),男,教授,主要研究方向为有机污染物降解机制与水污染控制技术研究、友好环境材料基础应用研究等。dghuang1017@163.com

Performance and mechanism of cathodic treatment of 2-chloro-4-nitrophenol contaminated wastewater in microbial electrolysis cells

  • 摘要: 2-氯-4-硝基苯酚(2C4NP)是一种典型的氯代硝基酚(CNPs)类污染物,具有持久性和较高的环境毒性。目前,关于微生物电解池系统(MECs)降解2C4NP的研究较少,其降解机理尚不明确。研究构建双室MECs,系统考察了外电压、2C4NP初始浓度及共基质种类对MECs阴极降解2C4NP的影响。通过扫描电镜(SEM)分析微生物形貌,并利用高效液相色谱(HPLC)、离子色谱(IC)和LC/MS/MS质谱分析技术对2C4NP及其降解中间体进行了定性和定量分析,提出了MECs阴极降解2C4NP的机制。结果表明:施加适当的外电压可显著促进2C4NP的降解,其初始浓度对降解速率影响显著,且不同共基质条件下降解过程符合不同的反应动力学规律。在最佳条件(外加电压0.5 V,共基质为葡萄糖,2C4NP初始浓度30 mg/L)下,2C4NP的72 h去除率和脱氯率分别达到96.77%和67.74%。SEM分析结果显示,阴极表面微生物呈现团聚态,增强了微生物之间的电子传递效率,为2C4NP高效降解提供了基础。HPLC、IC和LC/MS/MS分析表明,2C4NP在降解过程中产生了4-硝基苯酚、对乙酰氨基酚、2-氯酚等中间产物,部分脱除的氯和氮分别以Cl-和NO3-形式存在,这表明2C4NP在MECs阴极室的降解主要通过还原脱氯与脱硝基反应实现。研究初步揭示了双室MECs阴极降解2C4NP的机理,为氯代硝基酚类污染物的降解提供了理论依据和技术支持。
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  • 收稿日期:  2025-02-26
  • 网络出版日期:  2026-04-11
  • 刊出日期:  2026-02-01

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