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中国大陆降水中的全氟和多氟烷基物质(PFASs):未知前体和短链(C2-C3)全氟烷酸的贡献。

Per- and polyfluoroalkyl substances (PFASs) in precipitation from mainland China: Contributions of unknown precursors and short-chain (C2C3) perfluoroalkyl carboxylic acids.

机构信息

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

Department of Chemistry, Université de Montréal, Montréal, Québec, H3C 3J7, Canada.

出版信息

Water Res. 2019 Apr 15;153:169-177. doi: 10.1016/j.watres.2019.01.019. Epub 2019 Jan 24.

Abstract

A nationwide survey was conducted on per- and polyfluoroalkyl substances (PFASs) in precipitation across mainland China. Twenty-two PFASs, including precursors to perfluoroalkyl acids (pre-PFAAs), were investigated in thirty-nine precipitation samples collected from twenty-eight cities. Trifluoroacetate (TFA), perfluorooctanoic acid, and perfluorooctane sulfonic acid (PFOS) were ubiquitous in precipitation. TFA displayed the highest concentrations (8.8-1.8 × 10 ng/L), which were particularly elevated in coastal cities. 6:2 chlorinated polyfluorinated ether sulfonic acid, an alternative to PFOS, was detected for the first time in precipitation at a frequency of 43%. Polyfluoroalkyl phosphoric acid diesters and 6:2 fluorotelomer sulfonic acid were also occasionally detected. PFAS fluxes in the northeastern area (C4C12; 2.0 × 10-3.4 × 10 ng/m/d) with major PFAS manufacturing facilities were higher than those in the southwestern area (63-1.7 × 10 ng/m/d). Using total oxidizable precursor (TOP) assay, the occurrence of unknown pre-PFAAs was for the first time uncovered in precipitation with maximum estimated fluxes of C6 and C8 pre-PFAAs at 3.1 × 10 and 4.3 × 10 ng/m/d, respectively. The relative contribution of ultrashort-chain PFCAs (C2C3) ranged from 22% to 91% of ∑PFASs, while unknown pre-PFAAs accounted for 6%-56% of the total molar concentrations of PFASs. This bears critical concerns on underestimation of PFAS mass load from precipitation to surface environment ascribed to monitoring data solely on known PFASs. Unknown precursors of PFAAs in the atmosphere are yet to be identified for their chemical structures and relevant environmental risks as well.

摘要

在中国大陆进行了一项关于降水中超和全氟烷基物质 (PFAS) 的全国性调查。研究人员在 28 个城市采集的 39 个降水样本中检测了 22 种 PFAS,包括全氟烷基酸(PFAAs)的前体(前-PFAAs)。三氟乙酸 (TFA)、全氟辛酸 (PFOA) 和全氟辛烷磺酸 (PFOS) 在降水中普遍存在。TFA 的浓度最高(8.8-1.8×10 ng/L),在沿海城市尤为显著。作为 PFOS 的替代品,6:2 氯代全氟醚磺酸首次在降水中以 43%的频率被检测到。还偶尔检测到多氟烷基磷酸酯二酯和 6:2 氟代全氟磺酸。东北地区(C4C12;2.0×10-3.4×10 ng/m/d)的 PFAS 通量较高,该地区有主要的 PFAS 制造设施,而西南地区(63-1.7×10 ng/m/d)的通量较低。使用总可氧化前体(TOP)测定法,首次在降水中发现了未知的前 PFAAs,其 C6 和 C8 前 PFAAs 的最大估计通量分别为 3.1×10 和 4.3×10 ng/m/d。超短链 PFCAs(C2C3)在∑PFASs 中的相对贡献范围为 22%-91%,而未知前 PFAAs 占 PFASs 总摩尔浓度的 6%-56%。这就对仅基于已知 PFASs 的监测数据对降水向地表环境中 PFAS 质量负荷的低估提出了严峻的关注。大气中 PFAAs 的未知前体的化学结构及其相关环境风险也有待确定。

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