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A Global Mass Balance Analysis of the Source of Perfluorocarboxylic Acids in the Arctic Ocean

机译:北冰洋全氟羧酸来源的全球质量平衡分析

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Whereas the pervasive and abundant presence of perfluorinated carboxylic acids (PFCAs) in the Arctic marine food chain is clearly established, their origin and transport pathway into the Arctic Ocean are not. Either the atmospheric oxidation of volatile precursor compounds, such as the fluorotelomer alcohols (FTOHs), or the long-range oceanic transport of directly emitted PFCAs is seen as contributing the bulk of the PFCA input to the Arctic. Here simulations with the zonally averaged global fate and transport model Globo-POP, in combination with historical emission estimates for FTOHs and perfluorooctanoic acid (PFOA), are used to evaluate the relative efficiency and importance of the two transport pathways. Estimates of the emission-independent Arctic Contamination Potential reveal that the oceanic transport of directly emitted PFCAs is more than 10-fold more efficient than the atmospheric degradation of FTOHs in delivering PFCAs to the Arctic, mostly because of the low yield of the reaction. The cumulative historic emissions of FTOHs are lower than those estimated for PFOA alone by a factor of 2-3, further limiting the contribution that precursor oxidation makes to the total PFCAs load in the Arctic Ocean. Accordingly, when fed only with FTOH emissions, the model predicts FTOH air concentrations in agreement with the reported measurements, but yields Arctic seawater concentrations for the PFOA that are 2 orders of magnitude too low. Whereas ocean transport is thus very likely the dominant pathway of PFOA into the Arctic Ocean, the major transport route of longer chain PFCAs depends on the size of their direct emissions relative to those of 10:2 FTOH. The predicted time course of Arctic seawater concentrations is very similar for directly emitted and atmospherically generated PFCAs, implying that neither past doubling times of PFCA concentrations in Arctic marine mammals nor any future time trends are likely to resolve the question of the dominant source of PFCAs.
机译:北极海洋食物链中普遍存在和普遍存在的全氟羧酸(PFCA),但其来源和向北冰洋的运输途径尚不明确。挥发性前体化合物(如氟调聚物醇(FTOH))的大气氧化,或直接排放的PFCA的远距离海洋迁移都被认为是向北极提供大部分PFCA的原因。在此,使用区域平均全球命运和运输模型Globo-POP的模拟,结合FTOH和全氟辛酸(PFOA)的历史排放估算,来评估这两种运输途径的相对效率和重要性。与排放无关的北极污染潜能的估计表明,直接排放的PFCA的海洋运输效率比FTOH的大气降解高出PFOH到北极,这主要是由于反应产率低。 FTOH的累积历史排放量比单独的PFOA估计的历史排放量低2-3倍,进一步限制了前体氧化对北冰洋PFCA总量的贡献。因此,当仅喂入FTOH排放物时,该模型可以预测FTOH空气浓度,与报告的测量结果一致,但是对于PFOA而言,北极海水浓度太低两个数量级。因此,海洋运输很可能是全氟辛烷磺酸进入北冰洋的主要途径,而长链全氟辛烷磺酸的主要运输路线取决于其直接排放量相对于10:2 FTOH的直接排放量。对于直接排放和大气产生的全氟辛烷磺酸,北极海水浓度的预测时间过程非常相似,这意味着北极海洋哺乳动物中全氟辛烷磺酸浓度过去的翻倍时间或任何未来的时间趋势都不可能解决全氟辛烷磺酸的主要来源问题。

著录项

  • 来源
    《Environmental Science & Technology》 |2007年第13期|p.4529-4535|共7页
  • 作者

    FRANK WANIA;

  • 作者单位

    Department of Physical and Environmental Sciences, University of Toronto Scarborough, 1265 Military Trail, Toronto, Ontario, Canada M1C 1A4;

  • 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);
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境化学;
  • 关键词

  • 入库时间 2022-08-17 14:05:58

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