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中国大陆户外和室内灰尘中的全氟和多氟烷基物质:未知前体的贡献及其对人类暴露的影响。

Per- and Polyfluoroalkyl Substances in Outdoor and Indoor Dust from Mainland China: Contributions of Unknown Precursors and Implications for Human Exposure.

机构信息

MOE Key Laboratory of Pollution Processes and Environmental Criteria, College of Environmental Science and Engineering, Nankai University, Tianjin 300350, China.

出版信息

Environ Sci Technol. 2022 May 17;56(10):6036-6045. doi: 10.1021/acs.est.0c08242. Epub 2021 Mar 26.

Abstract

Per- and polyfluoroalkyl substances (PFASs) were analyzed in outdoor ( = 101) and indoor dust ( = 43, 38 paired with outdoors) samples across mainland China. From 2013 to 2017, the median concentration of ∑PFASs in outdoor dust tripled from 63 to 164 ng/g with an elevated contribution of trifluoroacetic acid and 6:2 fluorotelomer alcohol. In 2017, the indoor dust levels of ∑PFASs were in the range 185-913 ng/g, which were generally higher than the outdoor dust levels (105-321 ng/g). Emerging PFASs were found at high median levels of 5.7-97 ng/g in both indoor and outdoor dust samples. As first revealed by the total oxidized precursors assay, unknown perfluoroalkyl acid (PFAA)-precursors contributed 37-67 mol % to the PFAS profiles in indoor dust samples. A great proportion of C8 PFAA-precursors were precursors for perfluorooctanesulfonic acid, while C6 and C4 PFAA-precursors were mostly fluorotelomer based. Furthermore, daily perfluorooctanoic acid (PFOA) equivalent intakes of PFAAs (C4-C12) mixtures via indoor dust were first estimated at 1.3-1.5 ng/kg b.w./d for toddlers at high scenarios, which exceeds the derived daily threshold of 0.63 ng/kg b.w./d. from the European Food Safety Authority (EFSA). On this basis, an underestimation of 56%-69% likely remains without considering potential risks due to the biotransformation of unknown PFAA-precursors.

摘要

在中国大陆,对户外(=101)和室内灰尘(=43,38 个与户外配对)样本进行了全氟和多氟烷基物质(PFAS)分析。2013 年至 2017 年,户外灰尘中∑PFASs 的中位数浓度从 63ng/g 增加到 164ng/g,三氟乙酸和 6:2 氟代醇的贡献增加。2017 年,室内灰尘中∑PFASs 的浓度范围为 185-913ng/g,一般高于户外灰尘(105-321ng/g)。新兴的 PFASs 在室内和室外灰尘样本中的浓度中位数分别为 5.7-97ng/g。正如总氧化前体分析首次揭示的那样,室内和室外灰尘样本中的未知全氟烷基酸(PFAA)前体分别占 PFAS 谱的 37-67mol%。大量 C8 PFAA 前体是全氟辛烷磺酸的前体,而 C6 和 C4 PFAA 前体主要基于氟代醇。此外,通过室内灰尘,估计 PFAAs(C4-C12)混合物中全氟辛酸(PFOA)的每日等效摄入量在高情景下,幼儿为 1.3-1.5ng/kg b.w./d,超过了欧洲食品安全局(EFSA)规定的 0.63ng/kg b.w./d 的每日阈值。在此基础上,如果不考虑由于未知 PFAA 前体的生物转化而可能存在的潜在风险,那么可能仍然低估了 56%-69%。

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