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中国东部到西部地区户外灰尘中全氟和多氟烷基物质的全国分布。

Nationwide Distribution of Per- and Polyfluoroalkyl Substances in Outdoor Dust in Mainland China From Eastern to Western Areas.

机构信息

MOE Key Laboratory of Pollution Processes and Environmental Criteria, College of Environmental Science and Engineering, Nankai University , Tianjin 300071, China.

Department of Environmental Science and Engineering, Sichuan University , Chengdu, Sichuan 610065, China.

出版信息

Environ Sci Technol. 2016 Apr 5;50(7):3676-85. doi: 10.1021/acs.est.6b00649. Epub 2016 Mar 23.

Abstract

From eastern to western areas, per- and polyfluoroalkyl substances (PFASs) were detected at substantial levels in the outdoor dust across mainland China. Urban samples generally showed higher levels compared with those of rural samples. Compared with neutral PFASs, ionizable PFASs (C4-C12 perfluoroalkyl carboxylic acids and C4/C8 perfluoroalkyl sulfonic acids) were more abundant, with the highest total concentration up to 1.6 × 10(2) ng/g and perfluorooctanoic acid (PFOA) being a predominant analogue. Fluorotelomer alcohols (FTOHs) and polyfluoroalkyl phosphoric acid diesters (DiPAPs) were both detected in most samples with total concentrations of 0.12-32 and 0.030-20 ng/g, respectively. Perfluorooctane sulfonamidoethanols/sulfonamides (FOSE/As) were detected at low frequencies (<30%). In addition to partitioning to organic moiety, specific adsorption onto mineral particles can be important for PFASs to bind onto outdoor dust, especially for short-chain ionizable PFASs. The eastern plain areas were characterized by a higher contribution of long-chain ionizable PFASs; whereas the western high plateau areas were characterized by the dominating contribution of short-chain analogues. The difference suggests that the long-range atmospheric transport potential of PFASs from source regions to the inland is probably limited by the increase in altitude, and different sources from adjacent regions may influence the western border area of China.

摘要

从东部到西部地区,中国大陆户外灰尘中均检测到相当水平的全氟和多氟烷基物质 (PFASs)。城市样本的水平一般高于农村样本。与中性 PFASs 相比,可离子化的 PFASs(C4-C12 全氟烷酸和 C4/C8 全氟磺酸)更为丰富,总浓度最高可达 1.6×10(2)ng/g,其中全氟辛酸 (PFOA) 是主要的同系物。氟调聚物醇 (FTOHs) 和多氟烷基磷酸二酯 (DiPAPs) 在大多数样本中均有检出,总浓度分别为 0.12-32 和 0.030-20 ng/g。全氟辛烷磺酰胺基乙氧基/磺酰胺 (FOSE/As) 的检出频率较低(<30%)。除了分配到有机部分,特定于矿物颗粒的吸附对于 PFASs 结合到户外灰尘中也很重要,尤其是对于短链可离子化的 PFASs。东部平原地区的长链可离子化 PFASs 贡献较高;而西部高原地区则以短链同系物为主导。这种差异表明,PFASs 从源区到内陆的长程大气传输潜力可能受到海拔升高的限制,来自相邻地区的不同来源可能会影响中国的西部边境地区。

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