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UV/Nitrilotriacetic Acid Process as a Novel Strategy for Efficient Photoreductive Degradation of Perfluorooctanesulfonate

机译:紫外线/亚硝酸三乙酸工艺作为全氟辛烷磺酸有效光还原降解的新策略

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摘要

Perfluorooctanesulfonate (PFOS) is a toxic, bioaccumulative, and highly persistent anthropogenic chemical. Hydrated electrons ( e _(aq)~(–)) are potent nucleophiles that can effectively decompose PFOS. In previous studies, e _(aq)~(–) are mainly produced by photoionization of aqueous anions or aromatic compounds. In this study, we proposed a new photolytic strategy to generate e _(aq)~(–) and in turn decompose PFOS, which utilizes nitrilotriacetic acid (NTA) as a photosensitizer to induce water photodissociation and photoionization, and subsequently as a scavenger of hydroxyl radical (~(•)OH) to minimize the geminate recombination between ~(•)OH and e _(aq)~(–). The net effect is to increase the amount of e _(aq)~(–) available for PFOS degradation. The UV/NTA process achieved a high PFOS degradation ratio of 85.4% and a defluorination ratio of 46.8% within 10 h. A pseudo-first-order rate constant ( k ) of 0.27 h~(–1) was obtained. The laser flash photolysis study indicates that e _(aq)~(–) is the dominant reactive species responsible for PFOS decomposition. The generation of e _(aq)~(–) is greatly enhanced and its half-life is significantly prolonged in the presence of NTA. The electron spin resonance (ESR) measurement verified the photodissociation of water by detecting ~(•)OH. The model compound study indicates that the acetate and amine groups are the primary reactive sites.
机译:全氟辛烷磺酸(PFOS)是一种有毒,生物蓄积性和高度持久的人为化学物质。水合电子(e _(aq)〜(–))是有效的亲核试剂,可以有效分解PFOS。在先前的研究中,e _(aq)〜(–)主要是通过水性阴离子或芳族化合物的光电离而产生的。在这项研究中,我们提出了一种新的光解策略来生成e_(aq)〜(–),然后分解PFOS,该方法利用次氮基三乙酸(NTA)作为光敏剂来诱导水进行光解离和光电离,然后作为水的清除剂。羟基(〜(•)OH),以最大程度地减少〜(•OH)和e _(aq)〜(–)之间的联结重组。最终结果是增加了可用于PFOS降解的e _(aq)〜(–)的数量。 UV / NTA工艺在10小时内实现了85.4%的高PFOS降解率和46.8%的脱氟率。获得的伪一级速率常数(k)为0.27 h〜(-1)。激光闪光光解研究表明,e _(aq)〜(–)是负责全氟辛烷磺酸分解的主要反应物种。在存在NTA的情况下,e _(aq)〜(–)的生成大大增强,并且其半衰期大大延长。电子自旋共振(ESR)测量通过检测〜(•)OH验证了水的光解离。模型化合物的研究表明,乙酸酯基和胺基是主要的反应位点。

著录项

  • 来源
    《Environmental Science & Technology》 |2018年第5期|2953-2962|共10页
  • 作者单位

    State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China,Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China;

    State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China,Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China;

    State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China,Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China;

    State Key Laboratory of Pollution Control and Resources Reuse, College of Environmental Science and Engineering, Tongji University, Shanghai 200092, China,Shanghai Institute of Pollution Control and Ecological Security, Shanghai 200092, China;

    Shanghai Key Laboratory of Atmospheric Particle Pollution and Prevention, Department of Environmental Science & Engineering, Fudan University, Shanghai 200433, China;

    Linde-Robinson Laboratories, California Institute of Technology, Pasadena, California 91125, United States;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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