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评估过锰酸盐体系中全氟辛烷磺酸的氧化情况。

Evaluating perfluorooctanesulfonate oxidation in permanganate systems.

机构信息

Water Cycle Research Center, Korea Institute of Science and Technology, Seoul, South Korea.

Ecological Science and Engineering Interdisciplinary Graduate Program, Department of Agronomy, Purdue University, West Lafayette, IN, USA.

出版信息

Environ Sci Pollut Res Int. 2020 Apr;27(12):13976-13984. doi: 10.1007/s11356-020-07803-7. Epub 2020 Feb 8.

DOI:10.1007/s11356-020-07803-7
PMID:32034598
Abstract

Permanganate (PM) has shown to be able to oxidize a range of organic contaminants including perfluorooctane sulfonate (PFOS). However, mechanisms of PFOS removal by PM have been questioned. To provide clarity to what may be happening to PFOS in PM systems, here we evaluated the ability of PM on PFOS destruction by conducting studies similar to previous studies that reported PFOS destruction which included PM solutions and PM combined with persulfate (PS). We also evaluated if addition of various soluble catalysts could enhance PM's potential to breakdown PFOS. We observed no PFOS destruction by PM. We also show that the F and SO generation reported in a published study as evidence that PM was breaking bonds in PFOS were found below or not significantly higher than reported limits of quantitation and that SO impurities in technical PM approach the reported SO levels. For PM-PS systems, heterogeneous PFOS distribution was observed when subsampling reaction vessels at different depths and "salting-out" of PFOS was evident. In addition, subsequent sonication and filtering of the samples led to the apparent disappearance of most of the PFOS, which was an artifact arising from the behavior of PFOS aggregates or potential hemi-micelle formation. Given these findings, addition of salts may have application for collecting or concentrating PFOS and other PFAAs in a remediation or water treatment strategy.

摘要

高锰酸盐(PM)已被证明能够氧化包括全氟辛烷磺酸(PFOS)在内的一系列有机污染物。然而,PM 去除 PFOS 的机制一直存在争议。为了澄清 PM 系统中 PFOS 的可能变化情况,我们通过开展类似于先前报道 PFOS 破坏的研究来评估 PM 对 PFOS 破坏的能力,这些研究包括 PM 溶液和 PM 与过硫酸盐(PS)的结合。我们还评估了添加各种可溶性催化剂是否可以增强 PM 破坏 PFOS 的潜力。我们观察到 PM 没有破坏 PFOS。我们还表明,在一项已发表的研究中,作为 PM 破坏 PFOS 键的证据而报告的 F 和 SO 的生成,其含量低于或明显低于报告的定量限,并且技术 PM 中的 SO 杂质接近报告的 SO 水平。对于 PM-PS 系统,当在不同深度的反应容器中进行亚采样时,观察到异相 PFOS 分布,并且“盐析”PFOS 是明显的。此外,对样品进行后续的超声处理和过滤导致大部分 PFOS 明显消失,这是由于 PFOS 聚集体或潜在的半胶束形成的行为而产生的假象。鉴于这些发现,添加盐可能适用于在修复或水处理策略中收集或浓缩 PFOS 和其他 PFAAs。

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本文引用的文献

1
Developmental Toxicity of Perfluorooctanesulfonate (PFOS) and Its Chlorinated Polyfluoroalkyl Ether Sulfonate Alternative F-53B in the Domestic Chicken.全氟辛烷磺酸(PFOS)及其氯化的多氟烷基醚磺酸盐替代物 F-53B 在家禽中的发育毒性。
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Alternate Reductants with VB12 to Transform C8 and C6 Perfluoroalkyl Sulfonates: Limitations and Insights into Isomer-Specific Transformation Rates, Products and Pathways.
用 VB12 替代还原剂转化 C8 和 C6 全氟烷基磺酸盐:对同系物特异性转化速率、产物和途径的限制因素和深入了解。
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4
Perfluorooctane sulfonate (PFOS) removal with Pd/nFe nanoparticles: Adsorption or aqueous Fe-complexation, not transformation?钯/纳米铁颗粒去除全氟辛烷磺酸(PFOS):吸附还是水合铁络合,而不是转化?
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The mechanism and efficiency of MnO activated persulfate process coupled with electrolysis.MnO 活化过硫酸盐过程与电解耦联的机制和效率。
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Activated persulfate for organic chemical degradation: A review.用于有机化学降解的活化过硫酸盐:综述
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7
Modeling the Kinetics of Contaminants Oxidation and the Generation of Manganese(III) in the Permanganate/Bisulfite Process.基于过锰酸盐/亚硫酸盐工艺中污染物氧化动力学及锰(III)生成的模型构建。
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8
Heat-activated persulfate oxidation of PFOA, 6:2 fluorotelomer sulfonate, and PFOS under conditions suitable for in-situ groundwater remediation.在适合原位地下水修复的条件下,热活化过硫酸盐对全氟辛酸、6:2氟调聚物磺酸盐和全氟辛烷磺酸的氧化作用。
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9
Activation of Manganese Oxidants with Bisulfite for Enhanced Oxidation of Organic Contaminants: The Involvement of Mn(III).亚硫酸氢盐激活锰氧化物强化有机污染物氧化:Mn(III)的作用。
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ABTS as an Electron Shuttle to Enhance the Oxidation Kinetics of Substituted Phenols by Aqueous Permanganate.ABTS 作为电子穿梭体增强水溶液中高锰酸盐对取代酚类的氧化动力学。
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