Perfluorobutanesulfonate (PFBS) Treatment by Electrical Discharge Plasma: Reaction Mechanisms and Degradation Pathways

IF 4.3 3区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
ACS Omega Pub Date : 2025-08-13 DOI:10.1021/acsomega.5c03568
Diana Aranzales, Osakpolo Isowamwen, Sujan Fernando, David Speed, Thomas M. Holsen* and Selma Mededovic Thagard*, 
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引用次数: 0

Abstract

Electrical discharge plasmas rapidly degrade short-chain (SC) per- and polyfluoroalkyl substances (PFAS) in the presence of sacrificial surfactants. These surfactants facilitate the transport of PFAS to the plasma-liquid interface through electrostatic and hydrophobic interactions, where PFAS and surfactants are ultimately degraded. This study investigates the degradation of perfluorobutanesulfonate (PFBS) by nonthermal plasma, both in the absence and presence of quaternary alkyl trimethylammonium surfactants: octyl-, dodecyl-, and hexadecyl trimethylammonium bromide (C8TAB, C12TAB, and C16TAB, respectively). Advanced analytical techniques, including targeted, suspect, and nontargeted liquid chromatography-tandem mass spectrometry (LC-MS/MS), gas chromatography (GC-MS headspace), and ion chromatography (IC), were employed to identify the degradation byproducts of PFBS and the surfactants. Suspect and nontargeted analyses (NTA) revealed the formation of shorter-chain perfluorocarboxylic acids (PFCAs), products from H/F and OH/F exchange reactions, fluorinated ketones, fluorinated alcohols, unsaturated fluorinated compounds, and shorter-chain perfluorosulfonic acids (PFSAs); however, the last has been ascribed to contamination in the PFBS reagent. Notably, the degradation of PFBS, both in the absence and presence of surfactants, produced a nearly identical set of byproducts. Based on these newly identified byproducts, a series of degradation pathways has been proposed, involving solvated electrons and OH radicals as the primary reactive species. This study provides critical insights into the complex mechanisms and pathways of PFBS degradation during nonthermal plasma treatment. The findings have significant implications for optimizing plasma technologies and other PFAS treatment methods, with the proposed pathways expected to be relevant for PFAS degradation by technologies that utilize oxidative and nonoxidative species.

放电等离子体处理全氟丁烷磺酸:反应机制和降解途径
放电等离子体在牺牲表面活性剂的存在下迅速降解短链(SC)和多氟烷基物质(PFAS)。这些表面活性剂通过静电和疏水相互作用促进PFAS运输到等离子体-液体界面,PFAS和表面活性剂最终被降解。本研究研究了在不存在季烷基三甲基铵表面活性剂(分别为C8TAB、C12TAB和C16TAB)的情况下,非热等离子体对全氟丁烷磺酸(PFBS)的降解。采用先进的分析技术,包括靶向、可疑和非靶向液相色谱-串联质谱(LC-MS/MS)、气相色谱(GC-MS顶空)和离子色谱(IC)来鉴定PFBS和表面活性剂的降解副产物。可疑和非靶向分析(NTA)揭示了短链全氟羧酸(PFCAs)、氢/氟和氢氧/氟交换反应产物、氟化酮、氟化醇、不饱和氟化化合物和短链全氟磺酸(PFSAs)的形成;然而,最后一个被归因于PFBS试剂的污染。值得注意的是,在没有和存在表面活性剂的情况下,PFBS的降解都会产生一组几乎相同的副产物。基于这些新发现的副产物,提出了一系列的降解途径,其中溶剂化电子和OH自由基是主要的反应物质。这项研究为非热等离子体处理过程中PFBS降解的复杂机制和途径提供了重要的见解。这些发现对优化等离子体技术和其他PFAS处理方法具有重要意义,所提出的途径有望通过利用氧化和非氧化物质的技术降解PFAS。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
ACS Omega
ACS Omega Chemical Engineering-General Chemical Engineering
CiteScore
6.60
自引率
4.90%
发文量
3945
审稿时长
2.4 months
期刊介绍: ACS Omega is an open-access global publication for scientific articles that describe new findings in chemistry and interfacing areas of science, without any perceived evaluation of immediate impact.
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