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全规模垃圾渗滤液处理前后的全氟烷基和多氟烷基物质浓度。

Concentrations of perfluoroalkyl and polyfluoroalkyl substances before and after full-scale landfill leachate treatment.

机构信息

Department of Civil, Architectural, and Environmental Engineering, College of Engineering, University of Miami, Coral Gables, FL 33146, United States.

Department of Environmental Engineering Sciences, College of Engineering, University of Florida, Gainesville, FL 32611, United States.

出版信息

Waste Manag. 2022 Nov;153:110-120. doi: 10.1016/j.wasman.2022.08.024. Epub 2022 Sep 7.

Abstract

Many consumer and industrial products, industrial wastes and dewatered sludge from municipal wastewater treatment plants containing per- and polyfluoroalkyl substances (PFAS) are disposed of in landfills at the end of their usage, with PFAS in these products leached into landfill leachates. On-site leachate treatment is one possible method to reduce PFAS in leachates. Many landfills are equipped with on-site leachate treatment systems, but few full-scale facilities have been systematically evaluated for PFAS concentration changes. The objective of this study was to evaluate a cross-section of full-scale on-site landfill treatment systems to measure changes in PFAS concentrations. Leachate samples were collected before and after treatment from 15 facilities and were evaluated for 26 PFAS, including 11 perfluoroalkyl carboxylic acids (PFCAs), 7 perfluoroalkyl sulfonic acids (PFSAs), and 8 perfluoroalkyl acid precursors (PFAA-precursors). Transformation of precursors was evaluated by the total oxidizable precursor (TOP) assay. Results showed no obvious reductions in total measured PFAS (∑PFAS) for on-site treatment systems including ponds, aeration tanks, powdered activated carbon (PAC), and sand filtration. Among evaluated on-site treatment systems, only systems fitted with reverse osmosis (RO) showed significant reductions (98-99 %) of ∑PFAS in the permeate. Results from the TOP assay showed that untargeted PFAA-precursors converted into targeted short-chain PFCAs increasing ∑PFAS in oxidized samples by 30 %, on average. Overall, results of this study confirm the efficacy of RO systems and suggest the presence of additional precursors beyond those measured in this study.

摘要

许多含有全氟和多氟烷基物质 (PFAS) 的消费产品和工业产品、工业废物以及城市污水处理厂的脱水污泥,在使用寿命结束后被处置在垃圾填埋场中,这些产品中的 PFAS 会渗滤到垃圾渗滤液中。现场渗滤液处理是减少渗滤液中 PFAS 的一种可能方法。许多垃圾填埋场都配备了现场渗滤液处理系统,但很少有全面的设施对 PFAS 浓度变化进行系统评估。本研究的目的是评估一系列全面的现场垃圾填埋场处理系统,以测量 PFAS 浓度的变化。从 15 个设施中采集了处理前后的渗滤液样本,并对 26 种 PFAS 进行了评估,包括 11 种全氟烷基羧酸 (PFCAs)、7 种全氟烷基磺酸 (PFSAs) 和 8 种全氟烷基酸前体 (PFAA-前体)。通过总可氧化前体 (TOP) 测定评估前体的转化。结果表明,包括池塘、曝气池、粉末活性炭 (PAC) 和砂滤在内的现场处理系统对总测量的 PFAS (∑PFAS) 没有明显的降低。在所评估的现场处理系统中,只有配备反渗透 (RO) 的系统显示出∑PFAS 的显著降低(98-99%)在渗透物中。TOP 测定结果表明,未靶向的 PFAA-前体转化为靶向的短链 PFCAs,使氧化样品中的∑PFAS 平均增加了 30%。总体而言,本研究结果证实了 RO 系统的功效,并表明存在除本研究中测量的那些以外的其他前体。

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