Lai Senchao, Song Junwei, Song Tianli, Huang Zhijiong, Zhang Yingyi, Zhao Yan, Liu Guicheng, Zheng Junyu, Mi Wenying, Tang Jianhui, Zou Shichun, Ebinghaus Ralf, Xie Zhiyong
Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control, School of Environment and Energy, South China University of Technology, Guangzhou, China; Department of Multiphase Chemistry, Max Planck Institute for Chemistry, Mainz, Germany.
Guangdong Provincial Key Laboratory of Atmospheric Environment and Pollution Control, School of Environment and Energy, South China University of Technology, Guangzhou, China.
Environ Pollut. 2016 Jul;214:449-455. doi: 10.1016/j.envpol.2016.04.047. Epub 2016 Apr 23.
Neutral Polyfluoroalkyl substances (PFASs) in the atmosphere were measured during a cruise campaign over the northern South China Sea (SCS) from September to October 2013. Four groups of PFASs, i.e., fluorotelomer alcohols (FTOHs), fluorotelomer acrylates (FTAs), fluorooctane sulfonamides (FOSAs) and fluorooctane sulfonamidoethanols (FASEs), were detected in gas samples. FTOHs was the predominant PFAS group, accounting for 95.2-99.3% of total PFASs (ΣPFASs), while the other PFASs accounted for a small fraction of ΣPFASs. The concentrations of ΣPFASs ranged from 18.0 to 109.9 pg m(-3) with an average of 54.5 pg m(-3). The concentrations are comparable to those reported in other marine atmosphere. Higher concentrations of ΣPFASs were observed in the continental-influenced samples than those in other samples, pointing to the substantial contribution of anthropogenic sources. Long-range transport is suggested to be a major pathway for introducing gaseous PFASs into the atmosphere over the northern SCS. In order to further understand the fate of gaseous PFASs during transport, the atmospheric decay of neutral PFASs under the influence of reaction with OH radicals and atmospheric physical processes were estimated. Concentrations of 8:2 FTOH, 6:2 FTOH and MeFBSE from selected source region to the atmosphere over the SCS after long-range transport were predicted and compared with the observed concentrations. It suggests that the reaction with OH radicals may play an important role in the atmospheric decay of PFAS during long-range transport, especially for shorted-lived species. Moreover, the influence of atmospheric physical processes on the decay of PFAS should be further considered.
2013年9月至10月,在南海北部的一次巡航监测中对大气中的中性多氟烷基物质(PFASs)进行了测量。在气体样本中检测到了四类PFASs,即氟调聚物醇(FTOHs)、氟调聚物丙烯酸酯(FTAs)、氟辛烷磺酰胺(FOSAs)和氟辛烷磺酰胺基乙醇(FASEs)。FTOHs是主要的PFAS类别,占总PFASs(ΣPFASs)的95.2 - 99.3%,而其他PFASs在ΣPFASs中占比很小。ΣPFASs的浓度范围为18.0至109.9 pg m⁻³,平均为54.5 pg m⁻³。这些浓度与其他海洋大气中报告的浓度相当。在受大陆影响的样本中观察到的ΣPFASs浓度高于其他样本,这表明人为源的贡献很大。长距离传输被认为是气态PFASs进入南海北部大气的主要途径。为了进一步了解气态PFASs在传输过程中的归宿,估算了中性PFASs在与OH自由基反应和大气物理过程影响下的大气衰减。预测了长距离传输后从选定源区到南海大气中8:2 FTOH、6:2 FTOH和甲基全氟丁基磺酸乙酯(MeFBSE)的浓度,并与观测浓度进行了比较。这表明与OH自由基的反应可能在PFASs长距离传输过程中的大气衰减中起重要作用,特别是对于寿命较短物种。此外,应进一步考虑大气物理过程对PFASs衰减的影响。