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氟质量平衡分析与大气中的全氟和多氟烷基物质

Fluorine mass balance analysis and per- and polyfluoroalkyl substances in the atmosphere.

作者信息

Lin Huiju, Taniyasu Sachi, Yamazaki Eriko, Wu Rongben, Lam Paul K S, Eun Heesoo, Yamashita Nobuyoshi

机构信息

State Key Laboratory of Marine Pollution (SKLMP) and Department of Chemistry, City University of Hong Kong, Kowloon Tong, Hong Kong, China; National Institute of Advanced Industrial Science and Technology (AIST), 16-1 Onogawa, Tsukuba, Ibaraki 305-8569, Japan.

National Institute of Advanced Industrial Science and Technology (AIST), 16-1 Onogawa, Tsukuba, Ibaraki 305-8569, Japan.

出版信息

J Hazard Mater. 2022 Aug 5;435:129025. doi: 10.1016/j.jhazmat.2022.129025. Epub 2022 Apr 28.

Abstract

Given that only a small number of per- and polyfluoroalkyl substances (PFAS) are routinely monitored, levels of PFAS in the atmosphere may be underestimated. A protocol including analyses of target PFAS (n = 50), water-soluble fluoride, and total fluorine has been proposed and applied to atmospheric samples. The whole method recovery (including extraction recovery and sampling efficiency) of 90-110% were obtained for the majority of compounds (48/50) with low deviations between replicates (< 20%). Fluorotelomer alcohols were the most prevalent PFAS in the indoor air, while the outdoor air was dominated by the ultrashort-chain ionic PFAS (e.g., trifluoroacetic acid and perfluoropropanoic acid). Concentrations of organofluorine (OF) compounds calculated from the fluorine mass balance ranged from 1.74 ng F/m to 14.3 ng F/m and from 52.0 ng F/m to 1100 ng F/m in the particulate and gaseous phases, respectively, whereas only a minor proportion (around 1%) could be explained by target PFAS. In indoor air, OF compounds were observed in relatively high levels and with a shift to the fine particles (PM) . Our results reveal a large proportion of unidentified OF signatures in the atmosphere and suggest the need to use multiple approaches to improve our understanding of airborne fluorinated substances.

摘要

鉴于仅对少数全氟和多氟烷基物质(PFAS)进行常规监测,大气中PFAS的水平可能被低估。已提出一种包括分析目标PFAS(n = 50)、水溶性氟化物和总氟的方案,并将其应用于大气样品。大多数化合物(48/50)的全方法回收率(包括萃取回收率和采样效率)为90 - 110%,重复分析之间的偏差较低(< 20%)。氟调聚物醇是室内空气中最普遍的PFAS,而室外空气中则以超短链离子型PFAS(如三氟乙酸和全氟丙酸)为主。根据氟质量平衡计算的有机氟(OF)化合物浓度在颗粒相和气相中分别为1.74 ng F/m至14.3 ng F/m和52.0 ng F/m至1100 ng F/m,而目标PFAS仅占较小比例(约1%)。在室内空气中,观察到OF化合物含量相对较高,且向细颗粒物(PM)转移。我们的结果揭示了大气中很大一部分未识别的OF特征,并表明需要采用多种方法来增进我们对空气中含氟物质的了解。

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