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Partitioning Behavior of Per- and Polyfluoroalkyl Compounds between Pore Water and Sediment in Two Sediment Cores from Tokyo Bay, Japan

机译:日本东京湾两个沉积物芯中孔隙水和沉积物中全氟烷基化合物和多氟烷基化合物的分配行为

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摘要

The partitioning behavior of per- and polyfluoroalkyl compounds (PFCs) between pore water and sediment in two sediment cores collected from Tokyo Bay, Japan, was investigated. In addition, the fluxes and temporal trends in one dated sediment core were studied. Short-chain perfluoroalkyl carboxylic acids (PFCAs) (C ≤ 7) were found exclusively in pore water, while long-chain PFCAs (C ≥ 11) were found only in sediment. The perfluoroalkyl sulfonates (PFSAs), n-ethylperfluoro-1-octanesulfonamidoacetic acid (N-EtFOSAA), and perfluorooctane sulfonamide (PFOSA) seemed to bind more strongly to sediment than PFCAs. The enrichment of PFCs on sediment increased with increasing organic matter and decreasing pH. The perfluorocarbon chain length and functional group were identified as the dominating parameters that had an influence on the partitioning behavior of the PFCs in sediment The maximum ∑PFC contamination in sediment was observed in 2001 -2002 to be a flux of 197 pg cm~(-2) yr~(-1). Statistically significant increased concentrations in Tokyo Bay were found for perfluorooctanesulfonate (PFOS) (1956-2008), perfluorononanoic acid (PFNA) (1990-2008), and perfluoroundecanoic acid (PFUnDA) (1990-2008). Concentrations of PFOSA and N-EtF0SAA increased between 1985 and 2001, but after 2001, the concentration decreased significantly, which corresponded with the phase out of perfluorooctyl sulfonyl fluoride-based compounds by the 3M Company in 2000.
机译:研究了全氟烷基化合物和多氟烷基化合物(PFC)在孔隙水和沉积物之间的分配行为,这些孔隙水和沉积物来自日本东京湾,收集到两个沉积物核中。此外,还研究了一个过时沉积岩心的通量和时间趋势。仅在孔隙水中发现短链全氟烷基羧酸(PFCA)(C≤7),而仅在沉积物中发现长链PFCA(C≥11)。全氟烷基磺酸盐(PFSA),正乙基全氟-1-辛烷磺酰胺基乙酸(N-EtFOSAA)和全氟辛烷磺酰胺(PFOSA)似乎比PFCA更牢固地与沉积物结合。 PFCs在沉积物上的富集随着有机质的增加和pH的降低而增加。确定全氟化碳链长和官能团是影响沉积物中PFCs分配行为的主要参数。在2001年至2002年观察到沉积物中∑PFC的最大污染通量为197 pg cm〜(- 2)yr〜(-1)。在东京湾,全氟辛烷磺酸(PFOS)(1956-2008),全氟壬酸(PFNA)(1990-2008)和全氟十一烷酸(PFUnDA)(1990-2008)的浓度在统计学上有显着增加。在1985年至2001年之间,PFOSA和N-EtF0SAA的浓度有所增加,但是2001年之后,浓度显着下降,这与3M公司在2000年逐步淘汰基于全氟辛基磺酰氟的化合物相对应。

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  • 来源
    《Environmental Science & Technology》 |2009年第18期|6969-6975|共7页
  • 作者单位

    Institute for Coastal Research, GKSS Research Centre Geesthacht, DE-21502 Geesthacht, Germany Institute for Ecology and Environmental Chemistry, Leuphana University of Lueneburg, DE-21335 Lueneburg, Germany;

    National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan;

    Department of Biology and Chemistry, City University of Hong Kong, HKSAR, China;

    National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan;

    National Institute of Advanced Industrial Science and Technology (AIST), Tsukuba, Japan;

    Department of Biology and Chemistry, City University of Hong Kong, HKSAR, China;

    Institute for Coastal Research, GKSS Research Centre Geesthacht, DE-21502 Geesthacht, Germany;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
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