亚硝酸盐共存下UV/PS/CNTs降解 2,6-二氯苯酚及其机理
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四川大学建筑与环境学院

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X703

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国家自然科学基金项目(面上项目,重点项目,重大项目)


Degradation efficiency and mechanism of 2,6-DCP by UV/PS/CNTs under the coexistence of nitrite
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College of Architecture & Environment, Sichuan University

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The National Natural Science Foundation of China (General Program, Key Program, Major Research Plan)

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    摘要:

    以2,6-二氯苯酚(2,6-DCP)为目标污染物,在亚硝酸盐(NO2-)共存背景下采用紫外协同碳纳米管复合活化过硫酸盐工艺(UV/PS/CNTs)降解2,6-DCP,探究其影响因素及降解机理,考察体系循环活化潜能和副产物生成情况。结果表明,在反应时间30 min、反应温度25 ℃、2,6-DCP浓度为0.05 mmol/L、NO2-浓度为0.2 mmol/L、PS投量为0.5 mmol/L、CNTs投量为50 mg/L时,UV/PS/CNTs体系对2,6-DCP降解率达95.9%。该体系中,2,6-DCP降解速率随PS和CNTs浓度的增加而增大,随NO2-浓度增大而减小,溶液pH对目标物降解呈先增大后减小趋势,pH 9.0时降解率达99.8%,降解速率为0.3483 min-1。CNTs具有良好的循环使用性能,5次重复实验后仍能去除89.0%的2,6-DCP,且在实际水体中降解效果较好。机理分析表明,该体系对2,6-DCP降解遵循以单线态氧为主导的非自由基氧化途径,且反应过程中生成了一氯硝基酚副产物。

    Abstract:

    Taking 2,6-dichlorophenol (2,6-DCP) as the target pollutant to degrade 2,6-DCP in the background of nitrite (NO2-) coexistence by combined activation of persulfate process by UV and carbon nanotubes (UV/PS/CNTs). The influencing factors and degradation mechanism were investigated, and the cyclic activation potential and by-product generation of the system were investigated. The results showed that the reaction time was 30 min, reaction temperature was 25 ℃, the concentration of 2,6-DCP was 0.05 mmol/L, the concentration of NO2- was 0.2 mmol/L, the dosage of PS was 0.5 mmol/L, and the dosage of CNTs was 50 mg/L, the degradation rate of 2,6-DCP by UV/PS/CNTs system was 95.9%. In this system, the degradation rate of 2,6-DCP increased with the increase of PS and CNTs concentration, and decreased with the increase of NO2- concentration. The solution pH on the degradation of the target compounds showed a trend of increasing first and then decreasing,the degradation rate of 2,6-DCP was 99.8% and 0.3483 min-1 at pH 9.0. CNTs have good recycling performance, and 89.0% of 2,6-DCP could still be removed after 5 repeated experiments, the degradation effect in actual water is good. The mechanism analysis showed that the degradation of 2,6-DCP in this system followed a non-radical oxidation pathway dominated by singlet oxygen, and monochloronitrophenol by-products were generated during the reaction.

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田孜欣,陈滢.亚硝酸盐共存下UV/PS/CNTs降解 2,6-二氯苯酚及其机理[J].精细化工,2022,39(5):

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  • 收稿日期:2022-01-25
  • 最后修改日期:2022-04-02
  • 录用日期:2022-04-06
  • 在线发布日期: 2022-04-11
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