Collins Ashton, Krause Max J, Bessler Scott M, Brougham Andrew, McKnight Taryn, Strock Troy, Ateia Mohamed
Oak Ridge Associated Universities, US Environmental Protection Agency, Cincinnati, OH, USA.
Center for Environmental Solutions & Emergency Response, US Environmental Protection Agency, Cincinnati, OH, USA.
J Hazard Mater. 2024 Dec 5;480:136270. doi: 10.1016/j.jhazmat.2024.136270. Epub 2024 Oct 23.
The influence of elevated temperatures on PFAS leaching in municipal solid waste (MSW) landfills has not been well characterized in the published scientific literature. This study systematically examined the compositions and concentrations of per- and polyfluoroalkyl substances (PFAS) and precursors content in both normal temperature landfill and elevated temperature landfill (ETLF) leachates and compared to a municipal wastewater and to a WWTP influent with and without introduced leachates. The characterization of the samples involved the analysis of 71 PFAS target compounds before and after applying the total oxidizable precursor (TOP) assay, along with measuring fluorotelomer alcohols (FTOHs) and adsorbable organofluorine (AOF) levels. Summed PFAS concentrations in leachates were driven largely by fluorotelomer carboxylic acids (FTCAs), short-chain and ultrashort-chain perfluorinated carboxylic acids and sulfonic acids. Summed PFAS concentrations in ETLF leachate were significantly higher than in normal leachate for precursors and terminal PFAS products. TOP assay data demonstrated that ETLF leachate contained significantly higher concentrations of oxidizable PFAS precursors than normal leachate. PFAS profiles in leachates were distinct from municipal wastewater and from WWTP influent, suggesting diverse PFAS inputs to the WWTP. The presence of unknown precursors revealed by the TOP assay and AOF analyses highlights the complexity of PFAS sources impacting sewer networks, warranting further study to better characterize PFAS inputs to the WWTP on a city-wide scale.
高温对城市固体废弃物(MSW)填埋场中全氟和多氟烷基物质(PFAS)浸出的影响在已发表的科学文献中尚未得到充分描述。本研究系统地检测了常温填埋场和高温填埋场(ETLF)渗滤液中全氟和多氟烷基物质(PFAS)及其前体的组成和浓度,并与城市污水以及有无渗滤液引入情况下的污水处理厂进水进行了比较。样品表征包括在应用总可氧化前体(TOP)分析前后对71种PFAS目标化合物进行分析,同时测量氟调聚物醇(FTOH)和可吸附有机氟(AOF)水平。渗滤液中PFAS的总浓度主要由氟调聚物羧酸(FTCA)、短链和超短链全氟羧酸及磺酸驱动。ETLF渗滤液中PFAS前体和末端PFAS产物的总浓度显著高于正常渗滤液。TOP分析数据表明,ETLF渗滤液中可氧化PFAS前体的浓度显著高于正常渗滤液。渗滤液中的PFAS谱与城市污水和污水处理厂进水不同,表明进入污水处理厂的PFAS来源多样。TOP分析和AOF分析揭示的未知前体的存在凸显了影响下水道网络的PFAS来源的复杂性,有必要进一步研究以更好地描述城市范围内进入污水处理厂的PFAS输入情况。