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关于介质阻挡放电等离子体降解 C6/C6 PFPiA 机制的理论和实验研究。

Theoretical and experimental insights into the mechanisms of C6/C6 PFPiA degradation by dielectric barrier discharge plasma.

机构信息

College of Natural Resources and Environment, Northwest A&F University, Yangling, Shaanxi Province 712100, PR China; Key Laboratory of Plant Nutrition and the Agri-environment in Northwest China, Ministry of Agriculture, Yangling, Shaanxi 712100, PR China.

College of Information Science and Technology, Nanjing Forestry University, Nanjing 210037, PR China.

出版信息

J Hazard Mater. 2022 Feb 15;424(Pt B):127522. doi: 10.1016/j.jhazmat.2021.127522. Epub 2021 Oct 15.

DOI:10.1016/j.jhazmat.2021.127522
PMID:34879517
Abstract

As an emerging alternative legacy perfluoroalkyl substance, C6/C6 PFPiA (perfluoroalkyl phosphinic acids) has been detected in aquatic environments and causes potential risks to human health. The degradation mechanisms of C6/C6 PFPiA in a dielectric barrier discharge (DBD) plasma system were explored using validated experimental data and density functional theory (DFT) calculations. Approximately 94.5% of C6/C6 PFPiA was degraded by plasma treatment within 15 min at 18 kV. A relatively higher discharge voltage and alkaline conditions favored its degradation. C6/C6 PFPiA degradation was attributed to attacks of •OH, •O, and O. Besides PFHxPA and C2 -C6 shorter-chain perfluorocarboxylic acids, several other major intermediates including C4/C6 PFPiA, C4/C4 PFPiA, and C3/C3 PFPiA were identified. According to DFT calculations, the potential energy surface was proposed for possible reactions during C6/C6 PFPiA degradation in the discharge plasma system. Integrating the identified intermediates and DFT results, C6/C6 PFPiA degradation was deduced to occur by stepwise losing CF, free radical polymerization, and C-C bond cleavage. Furthermore, the DBD plasma treatment process decreased the toxicity of C6/C6 PFPiA to some extent. This study provides a comprehensive understanding of C6/C6 PFPiA degradation by plasma advanced oxidation.

摘要

作为一种新兴的替代传统全氟烷基物质,C6/C6 PFPiA(全氟膦酸)已在水生环境中被检测到,并对人类健康造成潜在风险。本研究采用验证后的实验数据和密度泛函理论(DFT)计算,探索了 C6/C6 PFPiA 在介质阻挡放电(DBD)等离子体系统中的降解机制。在 18 kV 下,等离子体处理 15 min 内可将约 94.5%的 C6/C6 PFPiA 降解。较高的放电电压和碱性条件有利于其降解。C6/C6 PFPiA 的降解归因于 •OH、•O 和 O 的攻击。除了 PFHxPA 和 C2-C6 短链全氟羧酸外,还鉴定了其他几种主要中间产物,包括 C4/C6 PFPiA、C4/C4 PFPiA 和 C3/C3 PFPiA。根据 DFT 计算,提出了在放电等离子体系统中 C6/C6 PFPiA 降解过程中可能发生的反应的势能面。综合鉴定的中间产物和 DFT 结果,推断 C6/C6 PFPiA 的降解是通过逐步失去 CF、自由基聚合和 C-C 键断裂来进行的。此外,DBD 等离子体处理过程在一定程度上降低了 C6/C6 PFPiA 的毒性。本研究为等离子体高级氧化法降解 C6/C6 PFPiA 提供了全面的认识。

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