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源区(中国天津)大气和干沉降样品中的中性和离子型全氟和多氟烷基物质(PFASs)

Neutral and ionic per- and polyfluoroalkyl substances (PFASs) in atmospheric and dry deposition samples over a source region (Tianjin, China).

作者信息

Yao Yiming, Chang Shuai, Sun Hongwen, Gan Zhiwei, Hu Hongwei, Zhao Yangyang, Zhang Yufen

机构信息

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

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

出版信息

Environ Pollut. 2016 May;212:449-456. doi: 10.1016/j.envpol.2016.02.023. Epub 2016 Mar 5.

Abstract

Per- and polyfluoroalkyl substances (PFASs) were detected in the atmosphere of a source region in Tianjin, China. Fluorotelomer alcohols (FTOHs) were the dominant neutral PFASs in the atmosphere with total concentrations of 93.6-131 pg/m(3) and 8:2 FTOH contributing the most, whereas perfluorooctane sulfonamide derivatives (PFOSAs) were two magnitudes lower or undetected. In comparison, ionic PFASs (perfluoroalkyl carboxyl acids (PFCAs)) in the atmosphere were detected at similar or even higher levels. At wastewater treatment plants (WWTPs), the air over influent was found with higher levels of FTOHs than over aeration tank and effluent; whereas in the air over the aeration tank, the concentrations of PFOSAs and nonvolatile ionic PFASs substantially increased, suggesting a possible direct release of ionic PFASs to the atmosphere besides the atmospheric conversion from volatile precursors. In the air phase, a low proportion (1-5%) of PFCAs was subjected to dry deposition in the source region. Interestingly, the dry-deposition-to-bulk-air ratios of PFCA analogues were the lowest at medium chain lengths (C8 and C9) and increased with either shorter or longer chain length. The extraordinary affinity of shorter-chain PFCAs (C6-C7) to particles was presumed to be due to their smaller molecular size favoring the interactions between the carboxyl head groups and specific sorption sites on particulate matter.

摘要

在中国天津的一个源区大气中检测到了全氟和多氟烷基物质(PFASs)。氟调聚物醇(FTOHs)是大气中主要的中性PFASs,总浓度为93.6 - 131 pg/m³,其中8:2 FTOH贡献最大,而全氟辛烷磺酰胺衍生物(PFOSAs)的浓度则低两个数量级或未被检测到。相比之下,大气中的离子型PFASs(全氟烷基羧酸(PFCAs))的检测水平与之相似甚至更高。在污水处理厂(WWTPs),进水上方空气中的FTOHs水平高于曝气池和出水上方的空气;而在曝气池上方的空气中,PFOSAs和非挥发性离子型PFASs的浓度大幅增加,这表明除了挥发性前体在大气中的转化外,离子型PFASs可能直接排放到大气中。在气相中,源区有低比例(1 - 5%)的PFCAs发生干沉降。有趣的是,PFCA类似物的干沉降与大气总量之比在中等链长(C8和C9)时最低,并且随着链长变短或变长而增加。推测短链PFCAs(C6 - C7)对颗粒物的超强亲和力是由于其较小的分子尺寸有利于羧基头部基团与颗粒物上特定吸附位点之间的相互作用。

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