Department of Chemistry, University of Toronto, Toronto, Ontario, Canada.
Environ Toxicol Chem. 2024 Nov;43(11):2297-2305. doi: 10.1002/etc.5815. Epub 2024 Feb 8.
Per- and polyfluoroalkyl substances (PFAS) are a class of chemicals present in a wide range of commercial and consumer products due to their water-repellency, nonstick, or surfactant properties, resulting from their chemical and thermal stability. This stability, however, often leads to persistence in the environment when they are inevitability released. We utilized microbial microcosms from wastewater treatment plant (WWTP) sludge to determine how employing different functional groups such as heteroatom linkages, varying chain lengths, and hydrofluoroethers (HFEs) will impact the ultimate fate of these novel PFAS structures. A suite of five novel fluorosurfactant building blocks (FCOCHFCFSCHCHOH (FESOH), FCOCHFCFSCHCHOH (MeFESOH), FCOCHFCFOCHCHOH (ProFdiEOH), FCOCHFCFCHOH (ProFEOH), and FCOCHFCFOCHCHOH (MeFdiEOH)) and their select transformation products, were incubated in WWTP aerobic microcosms to determine structure-activity relationships. The HFE alcohol congeners with a thioether (FESOH and MeFESOH) were observed to transform faster than the ether congeners, while also producing second-generation HFE acid products (FCOCHFC(O)OH (2H-3:2 polyfluoroalkyl ether carboxylic acid [PFECA]) and FCOCHFC(O)OH (2H-1:2 PFECA). Subsequent biodegradation experiments with 2H-1:2 PFESA and 2H-1:2 PFECA displayed no further transformation over 74 days. Surface water Photofate experiments compared 2H-1:2 PFECA, and 2H-1:2 polyfluorinated ether sulfonate (PFESA) with their fully fluorinated ether acid counterparts, and demonstrated the potential for both HFE acid species to completely mineralize over extended periods of time, a fate that highlights the value of studying novel PFAS functionalization. Environ Toxicol Chem 2024;43:2297-2305. © 2023 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC.
全氟和多氟烷基物质(PFAS)是一类存在于广泛的商业和消费产品中的化学物质,由于其具有疏水性、不粘性或表面活性剂特性,因此具有化学和热稳定性。然而,由于它们的化学稳定性,当它们不可避免地释放到环境中时,往往会在环境中持久存在。我们利用来自废水处理厂(WWTP)污泥的微生物微宇宙来确定采用不同的官能团,如杂原子键、不同的链长和氢氟醚(HFEs),将如何影响这些新型 PFAS 结构的最终命运。我们使用了一套五种新型氟表面活性剂构建块(FCOCHFCFSCHCHOH(FESOH)、FCOCHFCFSCHCHOH(MeFESOH)、FCOCHFCFOCHCHOH(ProFdiEOH)、FCOCHFCFCHOH(ProFEOH)和 FCOCHFCFOCHCHOH(MeFdiEOH))及其选定的转化产物,在 WWTP 好氧微宇宙中进行孵育,以确定结构-活性关系。具有硫醚的 HFE 醇同系物(FESOH 和 MeFESOH)比醚同系物转化得更快,同时也产生了第二代 HFE 酸产物(FCOCHFC(O)OH(2H-3:2 全氟烷基醚羧酸[PFECA])和 FCOCHFC(O)OH(2H-1:2 PFECA)。随后,在 74 天内,用 2H-1:2 PFESA 和 2H-1:2 PFECA 进行的后续生物降解实验没有进一步转化。地表水 Photofate 实验比较了 2H-1:2 PFECA 和 2H-1:2 全氟醚磺酸盐(PFESA)与其全氟醚酸对应物,证明了两种 HFE 酸物种在较长时间内完全矿化的潜力,这一命运凸显了研究新型 PFAS 功能化的价值。环境毒理化学 2024;43:2297-2305。©2023 作者。环境毒理化学由 Wiley Periodicals LLC 代表 SETAC 出版。