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Urban versus Remote Air Concentrations of Fluorotelomer Alcohols and Other Polyfluorinated Alkyl Substances in Germany

机译:德国城市中的氟调聚物和其他多氟烷基物质与偏远空气的浓度

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Neutral, volatile polyfluorinated alkyl substances (PFAS) were measured in environmental air samples at two different sites in Northern Germany in spring 2005. The sampling locations were chosen to cover a metropolitan and a rural site, the Hamburg city center, and Waldhof, a background monitoring site. An optimized and validated analytical protocol was used to analyze two sets of parallel high-volume air samples. For both sampling locations as well as for individual samples, field blanks were taken to monitor possible background contamination. Gas chromatography coupled to mass spectrometry using positive chemical ionization (GC/PCI-MS) was used for quantitative analyses. This article describes the first air concentration data of volatile PFAS outside North America reported in the peer-reviewed literature. The wide distribution of fluorotelomer alcohols (FTOHs), fluorinated sulfonamides, and sulfonamidoethanols (FOSAs/FOSEs) in German environmental air is presented. Furthermore, two volatile PFAS, i.e., N-methyl fluorooctane sulfonamide (NMeFOSA) and 4:2 FTOH, were determined for the first time in environmental air. Minimum-maximum ΣFTOH concentrations of 64-311 pg/m~3 (remote) up to 150-546 pg/m~3 (urban) and minimum—maximum ΣFOSA + FOSE concentrations between 12 and 54 pg/m~3 (remote) and 29 and 151 pg/m~3 (urban) were determined. 8:2 FTOH and 6:2 FTOH were found to be the predominant POPs determined in Waldhof so far. Blank contamination was found to be negligible. A significant correlation was found with the ambient temperature for the partitioning of airborne FOSEs between the gaseous and particulate phase (R = 0.853), whereas FTOHs and FOSAs were almost exclusively found in the gaseous phase. Furthermore, highest airborne PFAS concentrations were determined at relatively high ambient temperatures. Correlation coefficients (R) for ΣFTOH and ΣFOSA + FOSE concentrations with temperature were 0.954 and 0.968, respectively. Finally, the PFAS concentrations determined in this study are set into context with levels of "classical" persistent organic pollutants (POPs) in the same region and PFAS data available for North America.
机译:在2005年春季,对德国北部两个不同地点的环境空气样品进行了中性,挥发性多氟烷基物质(PFAS)的测量。采样地点的选择是覆盖大都市和农村地区,汉堡市中心以及Waldhof(背景)监视站点。经过优化和验证的分析协议用于分析两组平行的大量空气样本。对于两个采样地点以及单个样本,均采用现场空白来监视可能的背景污染。使用正化学电离(GC / PCI-MS)联用气相色谱和质谱进行定量分析。本文介绍了同行评审文献中报道的北美以外地区挥发性PFAS的第一批空气浓度数据。介绍了在德国环境空气中氟调聚物醇(FTOH),氟化磺酰胺和磺酰胺基乙醇(FOSA / FOSE)的广泛分布。此外,首次在环境空气中测定了两种挥发性PFAS,即N-甲基氟辛烷磺酰胺(NMeFOSA)和4:2 FTOH。最小最大ΣFTOH浓度为64-311 pg / m〜3(远程),最高为150-546 pg / m〜3(城市)以及最小ΣFOSA+ FOSE的最大最大浓度为12至54 pg / m〜3(远程)确定为29和151 pg / m〜3(城市)。迄今为止,发现8:2 FTOH和6:2 FTOH是Waldhof确定的主要POPs。发现空白污染可以忽略不计。发现与环境温度之间的关系是气态FOSE在气相和颗粒相之间的分配(R = 0.853),而FTOH和FOSA几乎仅在气相中存在。此外,在相对较高的环境温度下确定了最高的机载PFAS浓度。 ΣFTOH和ΣFOSA+ FOSE浓度与温度的相关系数(R)分别为0.954和0.968。最后,将本研究中确定的PFAS浓度与同一地区的“经典”持久性有机污染物(POPs)的水平和北美可用的PFAS数据结合起来。

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