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等离子体辅助降解短链全氟烷基物质 (PFAS):全氟丁烷磺酸 (PFBS)。

Plasma-assisted degradation of a short-chain perfluoroalkyl substance (PFAS): Perfluorobutane sulfonate (PFBS).

机构信息

Department of Chemical and Biomolecular Engineering, Plasma Research Laboratory, Clarkson University, 8 Clarkson Avenue, Potsdam, NY 13699, USA.

Department of Civil and Environmental Engineering, Clarkson University, 8 Clarkson Avenue, Potsdam, NY 13699, USA.

出版信息

J Hazard Mater. 2023 Aug 15;456:131691. doi: 10.1016/j.jhazmat.2023.131691. Epub 2023 May 23.

Abstract

This study investigates the degradation of perfluorobutane sulfonate (PFBS), a chemical compound belonging to a group of per- and polyfluoroalkyl substances (PFAS), by gas-phase electrical discharge plasma. Plasma alone was ineffective in degrading PFBS due to its poor hydrophobicity, which inhibited the compound from accumulating at the plasma-liquid interface, the region of chemical reactivity. To overcome bulk liquid mass transport limitations, a surfactant, hexadecyltrimethylammonium bromide (CTAB), was introduced to interact with and transport PFBS to the plasma-liquid interface. In the presence of CTAB, ∼99% of PFBS was removed from the bulk liquid and concentrated at the interface, where 67% of the concentrate was degraded and 43% of that amount was defluorinated within one hour. PFBS degradation was further improved by optimizing the surfactant concentration and dosage. Experiments with a range of cationic, non-ionic, and anionic surfactants revealed that the PFAS-CTAB binding mechanism is predominantly electrostatic. A mechanistic understanding of the PFAS-CTAB complex formation, its transport to and destruction at the interface is proposed, alongside the chemical degradation scheme, which includes the identified degradation byproducts. This study shows that surfactant-assisted plasma treatment is one of the most promising techniques for destroying short-chain PFAS in contaminated water.

摘要

本研究探讨了气相放电等离子体对全氟丁烷磺酸(PFBS)的降解作用,PFBS 是全氟和多氟烷基物质(PFAS)的一种化合物。由于其较差的疏水性,单独的等离子体无法有效降解 PFBS,这抑制了该化合物在等离子体-液体界面处的积累,即化学反应区域。为了克服体相液体传质限制,引入了表面活性剂十六烷基三甲基溴化铵(CTAB),以与 PFBS 相互作用并将其输送到等离子体-液体界面。在 CTAB 的存在下,约 99%的 PFBS 从体相液体中被去除并浓缩在界面处,其中 67%的浓缩物被降解,而其中 43%的量在一小时内脱氟。通过优化表面活性剂浓度和剂量进一步提高了 PFBS 的降解。用一系列阳离子、非离子和阴离子表面活性剂进行的实验表明,PFAS-CTAB 的结合机制主要是静电的。提出了一种对 PFAS-CTAB 配合物形成、其向界面的传输以及在界面处的破坏的机理理解,以及包括已确定的降解副产物在内的化学降解方案。本研究表明,表面活性剂辅助的等离子体处理是破坏受污染水中短链 PFAS 的最有前途的技术之一。

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