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两家含氟聚合物制造工厂对河流下游以及饮用水资源中全氟和多氟烷基物质污染的影响。

The impact of two fluoropolymer manufacturing facilities on downstream contamination of a river and drinking water resources with per- and polyfluoroalkyl substances.

作者信息

Bach Cristina, Dauchy Xavier, Boiteux Virginie, Colin Adeline, Hemard Jessica, Sagres Véronique, Rosin Christophe, Munoz Jean-François

机构信息

Nancy Laboratory for Hydrology, Water Chemistry Department, ANSES, 40 rue Lionnois, 54000, Nancy, France.

出版信息

Environ Sci Pollut Res Int. 2017 Feb;24(5):4916-4925. doi: 10.1007/s11356-016-8243-3. Epub 2016 Dec 17.

Abstract

Perfluoroalkyl and polyfluoroalkyl substances (PFASs) are emerging contaminants that have been detected in the environment, biota, and humans. Drinking water is a route of exposure for populations consuming water contaminated by PFAS discharges. This research study reports environmental measurement concentrations, mass flows, and the fate of dozens of PFASs in a river receiving effluents from two fluoropolymer manufacturing facilities. In addition to quantified levels of PFASs using LC- and GC-MS analytical methods, the total amount of unidentified PFASs and precursors was assessed using two complementary analytical methods, absorbable organic fluorine (AOF) determination and oxidative conversion of perfluoroalkyl carboxylic acid (PFCA) precursors. Several dozen samples were collected in the river (water and sediment) during four sampling campaigns. In addition, samples were collected in two well fields and from the outlet of the drinking water treatment plants after chlorination. We estimated that 4295 kg PFHxA, 1487 kg 6:2FTSA, 965 kg PFNA, 307 kg PFUnDA, and 14 kg PFOA were discharged in the river by the two facilities in 2013. High concentrations (up to 176 ng/g dw) of odd long-chain PFASs (PFUnDA and PFTrDA) were found in sediment samples. PFASs were detected in all 15 wells, with concentrations varying based on the location of the well in the field. Additionally, the presence of previously discharged PFASs was still measurable. Significant discrepancies between PFAS concentration profiles in the wells and in the river suggest an accumulation and transformation of PFCA precursors in the aquifer. Chlorination had no removal efficiency and no unidentified PFASs were detected in the treated water with either complementary analytical method. Although the total PFAS concentrations were high in the treated water, ranging from 86 to 169 ng/L, they did not exceed the currently available guideline values.

摘要

全氟烷基和多氟烷基物质(PFASs)是已在环境、生物群和人体中被检测到的新兴污染物。饮用水是食用受PFAS排放污染水的人群的一种暴露途径。本研究报告了一条接纳来自两家含氟聚合物制造设施废水的河流中数十种PFASs的环境测量浓度、质量流量及归宿。除了使用液相色谱和气相色谱 - 质谱分析方法对PFASs进行定量分析外,还使用两种互补分析方法——可吸收有机氟(AOF)测定和全氟烷基羧酸(PFCA)前体的氧化转化,评估了未识别的PFASs和前体的总量。在四次采样活动期间,在该河流(水和沉积物)中采集了几十个样本。此外,还在两个井场以及饮用水处理厂氯化处理后的出水口采集了样本。我们估计,2013年这两家设施向该河流排放了4295千克全氟己酸(PFHxA)、1487千克6:2氟调聚物磺酸(6:2FTSA)、965千克全氟萘酸(PFNA)、307千克全氟十一烷酸(PFUnDA)和14千克全氟辛酸(PFOA)。在沉积物样本中发现了高浓度(高达176纳克/克干重)的奇数长链PFASs(PFUnDA和全氟十三烷酸(PFTrDA))。在所有15口井中均检测到了PFASs,其浓度因井在井场中的位置而异。此外,之前排放的PFASs仍可检测到。井中和河流中PFAS浓度分布之间的显著差异表明PFCA前体在含水层中发生了积累和转化。氯化处理没有去除效率,且使用任何一种互补分析方法在处理后的水中均未检测到未识别的PFASs。尽管处理后的水中PFAS总浓度较高,范围为86至169纳克/升,但未超过目前可用的指导值。

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