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3
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Abiotic Hydrolysis of Fluorotelomer-Based Polymers as a Source of Perfluorocarboxylates at the Global Scale.全球化尺度下基于氟调聚物的聚合物的非生物水解作用作为全氟羧酸根的来源。
Environ Sci Technol. 2015 Dec 15;49(24):14129-35. doi: 10.1021/acs.est.5b03686. Epub 2015 Nov 24.

确定全球背景土壤中全氟辛烷磺酸的负荷以及可以解释这些负荷的基于氟端基聚合物的降解速率。

Determining global background soil PFAS loads and the fluorotelomer-based polymer degradation rates that can account for these loads.

机构信息

National Exposure Research Laboratory, USEPA, 960 College Station Road, Athens, GA 30605, United States of America.

Department of Chemistry, University of Toronto, 80 St. George Street, Toronto, Ontario M5S 3H6, Canada.

出版信息

Sci Total Environ. 2019 Feb 15;651(Pt 2):2444-2449. doi: 10.1016/j.scitotenv.2018.10.071. Epub 2018 Oct 10.

DOI:10.1016/j.scitotenv.2018.10.071
PMID:30336434
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7957346/
Abstract

In recent years, fluorotelomer-based polymers (FTPs) have been the dominant product of the fluorotelomer industry. For the last decade, whether FTPs degrade to toxic perfluorocarboxylates (PFCAs) has been vigorously contested, with early studies arguing that FTPs have half-lives >1000 years, and others concluding decadal half-lives. Given this FTP half-life discrepancy of 10- to >100-fold, here we investigate whether environmental loads of long-chain PFCAs might offer an independent approach to assess FTP half-lives. Specifically we: i) use surface soil-PFCA data to estimate terrestrial surface-soil background PFCA concentrations and loads; ii) extrapolate these data to generate global PFCA load estimates; iii) compare these estimates to published ocean-derived and industrial-emissions load estimates, finding agreement for perfluorooctanoate (C8), but an excess in longer-chain (C10,C12) PFCAs for ocean- and soil-derived loads relative to emissions; iv) model FTP degradation rates required to reconcile this discrepancy; and iv) compare our modeled estimates to existing experimental results. These findings show agreement for FTP half-lives at the decades-scale supporting existing laboratory studies that report decade-scale half-lives for FTPs. This suggests that global long-chain PFCA loads will increase for decades if legacy FTPs already manufactured are not contained upon disposal. These results suggest that FTPs comprised of novel poly- and perfluorinated alkyl substances (PFASs) now in production might constitute considerable sources to the environment of the new generation of PFASs.

摘要

近年来,含氟端基聚合物(FTPs)一直是氟调聚物行业的主要产品。在过去的十年中,FTPs 是否会降解为有毒的全氟羧酸(PFCAs)一直存在激烈争议,早期研究认为 FTPs 的半衰期>1000 年,而其他研究则得出了数十年的半衰期。鉴于 FTP 半衰期相差 10 到>100 倍,我们在这里研究长链 PFCAs 的环境负荷是否可以提供一种独立的方法来评估 FTP 半衰期。具体来说,我们:i)使用表层土壤-PFCA 数据估算陆地表层土壤背景 PFCA 浓度和负荷;ii)推断这些数据以生成全球 PFCA 负荷估算值;iii)将这些估算值与已发表的海洋衍生和工业排放负荷估算值进行比较,发现对于全氟辛烷酸(C8),海洋和土壤衍生负荷与排放之间存在一致性,但对于较长链(C10,C12)PFCAs 则存在过量;iv)建模需要降解的 FTP 速率以解决这种差异;iv)将我们的模型估算值与现有实验结果进行比较。这些发现表明,FTP 半衰期在数十年的范围内是一致的,支持了现有实验室研究报告的 FTP 半衰期为数十年。这表明,如果已经制造的传统 FTPs 在处置时不加以控制,那么几十年内全球长链 PFCA 负荷将增加。这些结果表明,现在生产的新型多氟和全氟烷基物质(PFASs)组成的 FTPs 可能会成为新一代 PFASs 向环境中排放的重要来源。