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Polyfluorinated Compounds In Ambient Air From Ship- And Land-based Measurements In Northern Germany

机译:来自德国北部船上和陆上测量的环境空气中的多氟化合物

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摘要

Neutral volatile and semi-volatile polyfluorinated organic compounds (PFC) and ionic perfluorinated compounds were determined in air samples collected at two sites in the vicinity of Hamburg, Germany, and onboard the German research vessel Atair during a cruise in the German Bight, North Sea, in early November 2007. PUF/XAD-2/PUF cartridges and glass fiber filters as sampling media were applied to collect several fluorotelomer alcohols (FTOH), fluorotelomer acrylates (FTA), perfluoroalkyl sulfonamides (FASA), and perfluoroalkyl sulfonamido ethanols (FASE) in the gas- and particle-phase as well as a set of perfluorinated carboxylates (PFCA) and sulfonates (PFSA) in the particle-phase. This study presents the distribution of PFC in ambient air of the German North Sea and in the vicinity of Hamburg for the first time. Average total PFC concentrations in and around Hamburg (180 pg m~(-3)) were higher than those observed in the German Bight (80 pg m~(-3)). In the German Bight, minimum-maximum gas-phase concentrations of 17-82 pg m~(-3) for ΣFTOH, 2.6-10 pg m~(-3) for ΣFTA, 10-15 pg m~(-3 )for ΣFASA, and 2-4.4 pg m~3 for ΣFASE were determined. In the vicinity of Hamburg, minimum-maximum gas-phase concentrations of 32-204 pg m~(-3) for ΣFTOH, 3-26 pg m~(-3) for 2FTA, 3-18 pg m~(-3) for ΣFASA, and 2-15 pg m~(-3) for ΣFASE were detected. Concentrations of perfluorinated acids were in the range of 1-11 pg m~(-3). FTOH clearly dominated the substance spectrum; 8:2 FTOH occurred in maximum proportions. Air mass back trajectories, cluster, and correlation analyses revealed that the air mass origin and thus medium to long range atmospheric transport was the governing parameter for the amount of PFC in ambient air. Southwesterly located source regions seemed to be responsible for elevated PFC concentrations, local sources appeared to be of minor importance.
机译:在德国汉堡附近两个地点采集的空气样本中确定了中性挥发性和半挥发性的多氟有机化合物(PFC)和离子全氟化合物,并在北海德国海岸线的航行中在德国研究船Atair上进行了测定,于2007年11月上旬。使用PUF / XAD-2 / PUF滤芯和玻璃纤维过滤器作为采样介质,以收集几种氟代端基醇(FTOH),氟代端基丙烯酸酯(FTA),全氟烷基磺酰胺(FASA)和全氟烷基磺酰胺基乙醇(FASE) )在气相和颗粒相中以及一组在颗粒相中的全氟化羧酸盐(PFCA)和磺酸盐(PFSA)。这项研究首次提出了德国北海和汉堡附近环境空气中PFC的分布。汉堡及其周边地区的平均全氟化合物浓度(180 pg m〜(-3))高于德国海岸线(80 pg m〜(-3))。在德国湾中,ΣFTOH的最小最大气相浓度为17-82 pg m〜(-3),ΣFTA的最小最大气相浓度为2.6-10 pg m〜(-3),10FT的最大气相浓度为10-15 pg m〜(-3)确定了ΣFASA和ΣFASE的2-4.4 pg m〜3。在汉堡附近,ΣFTOH的最小最大气相浓度为32-204 pg m〜(-3),2FTA的最小最大气相浓度为3-26 pg m〜(-3),3-18 pg m〜(-3)对于ΣFASA,检测到2-15 pg m〜(-3)。全氟酸的浓度范围为1-11 pg m〜(-3)。 FTOH明显主导了物质范围。 8:2 FTOH以最大比例出现。空气质量的反向轨迹,聚类和相关分析表明,空气质量的起源以及中长期的大气迁移是环境空气中PFC量的控制参数。位于西南的源地区似乎是造成PFC浓度升高的原因,而本地来源似乎次要。

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