Patch David, O'Connor Natalia, Ahmed Ellie, Houtz Erika, Bentel Michael, Ross Ian, Scott Jennifer, Koch Iris, Weber Kela
Environmental Sciences Group, Department of Chemistry and Chemical Engineering, Royal Military College of Canada, Kingston, ON K7K 7B4, Canada.
ECT2, 125 Industrial Way, Portland, ME 04103, United States of America.
Sci Total Environ. 2024 Oct 10;946:174079. doi: 10.1016/j.scitotenv.2024.174079. Epub 2024 Jun 20.
As per- and polyfluoroalkyl substances (PFAS) infiltrate the environment via industrial, commercial, and domestic sources, the demand for robust, cost-effective, and straightforward analytical assays intensifies to enhance PFAS characterization and quantification. To address this demand, this study introduces a novel UV-HO-TOP assay, identifying optimal parameters such as pH (5-9), oxidant concentration (500 mM HO), activation rate (63 mM HO h), and an acceptable total organic carbon (TOC) limit (~1000 mg/L TOC) to achieve maximum PFAA precursor conversion. Additional work was performed further optimizing the UV-TOP assay, by confirming its superiority to heat activation, identifying the effectiveness of different persulfate salts, and investigating different concentrations of sodium persulfate and sodium hydroxide at a 1:2.5 ratio on PFCA yield. Our investigation concluded by applying the UV-HO-TOP assay, using sodium persulfate as the TOP assay oxidant, to 6:2 FTS and five different AFFF samples. High-resolution mass spectrometry and an expanded analytical suite support sample analysis, facilitating direct quantification of ultra-short chain perfluoroalkyl carboxylates (PFCAs) and common fluorotelomer compounds including 5:3/5:1:2 fluorotelomer betaine and 6:2 fluorotelomer sulfonamido betaine. Results highlight several advantages of this tandem UV-activated method, including enhanced preservation of perfluoroalkyl chains (post-oxidation of 6:2 fluorotelomer sulfonate resulted in 28 % PFHpA, 47 % PFHxA, 25 % C3-C5 PFCA), capacity to handle high TOC limits (1000 mg/L TOC), and ability to incorporate higher persulfate concentrations in a single oxidation cycle.
随着全氟和多氟烷基物质(PFAS)通过工业、商业和家庭来源渗透到环境中,对强大、经济高效且简单的分析检测方法的需求日益增加,以加强PFAS的表征和定量。为满足这一需求,本研究引入了一种新型的UV-HO-TOP检测方法,确定了最佳参数,如pH值(5-9)、氧化剂浓度(500 mM HO)、活化速率(63 mM HO h)和可接受的总有机碳(TOC)限值(~1000 mg/L TOC),以实现全氟烷基酸前体的最大转化率。通过确认其相对于热活化的优越性、确定不同过硫酸盐的有效性以及研究1:2.5比例的不同浓度过硫酸钠和氢氧化钠对全氟辛酸产量的影响,进一步开展了优化UV-TOP检测方法的工作。我们的研究通过将UV-HO-TOP检测方法(使用过硫酸钠作为TOP检测氧化剂)应用于6:2 FTS和五个不同的AFFF样品而告终。高分辨率质谱和扩展的分析套件支持样品分析,便于直接定量超短链全氟烷基羧酸盐(PFCA)以及常见的氟调聚物化合物,包括5:3/5:1:2氟调聚物甜菜碱和6:2氟调聚物磺酰胺甜菜碱。结果突出了这种串联UV活化方法的几个优点,包括增强全氟烷基链的保留(6:2氟调聚物磺酸盐氧化后产生28%的全氟己基丙酸、47%的全氟己酸、25%的C3-C5 PFCA)、处理高TOC限值(1000 mg/L TOC)的能力以及在单个氧化循环中纳入更高过硫酸盐浓度的能力。