Aranzales Diana, Isowamwen Osakpolo, Fernando Sujan, Speed David, Holsen Thomas M, Mededovic Thagard Selma
Department of Chemical and Biomolecular Engineering, Plasma Research Laboratory, Clarkson University, 8 Clarkson Avenue, Potsdam, New York 13699, United States.
Department of Civil and Environmental Engineering, Clarkson University, 8 Clarkson Avenue, Potsdam, New York 13699, United States.
ACS Omega. 2025 Aug 13;10(33):37524-37535. doi: 10.1021/acsomega.5c03568. eCollection 2025 Aug 26.
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.
在牺牲性表面活性剂存在的情况下,放电等离子体可快速降解短链全氟和多氟烷基物质(PFAS)。这些表面活性剂通过静电和疏水相互作用促进PFAS向等离子体 - 液体界面的传输,PFAS和表面活性剂最终在此处被降解。本研究调查了在不存在和存在季铵烷基三甲基铵表面活性剂(分别为辛基、十二烷基和十六烷基三甲基溴化铵,即C8TAB、C12TAB和C16TAB)的情况下,非热等离子体对全氟丁烷磺酸(PFBS)的降解情况。采用了先进的分析技术,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(顶空气相色谱 - 质谱,GC - MS headspace)和离子色谱(IC),以鉴定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(PFCA)的形成、H/F和OH/F交换反应的产物、氟化酮、氟化醇、不饱和氟化化合物以及短链全氟磺酸(PFSA);然而,后者被归因于PFBS试剂中的污染。值得注意的是,无论是否存在表面活性剂,PFBS的降解都产生了几乎相同的一组副产物。基于这些新鉴定的副产物,提出了一系列降解途径,涉及溶剂化电子和OH自由基作为主要反应物种。本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关键见解。这些发现对于优化等离子体技术和其他PFAS处理方法具有重要意义,所提出的途径预计与利用氧化和非氧化物种的技术对PFAS的降解相关。