环境化学
沉积物
吸附
生物地球化学循环
萃取(化学)
水槽(地理)
河口
化学
污染
环境科学
地质学
色谱法
海洋学
生态学
生物
地貌学
吸附
有机化学
地图学
地理
作者
J. Harfmann,Kate Tito,Robert J. Kieber,G. Brooks Avery,Ralph N. Mead,Megumi S. Shimizu,Stephen A. Skrabal
标识
DOI:10.1021/acsearthspacechem.0c00323
摘要
The sedimentary fate of hexafluoropropylene oxide dimer acid (HFPO-DA) was investigated over a 12 week time series in HFPO-DA-amended (600 ng of spike addition) freshwater and estuarine tidal sediments collected in southeastern North Carolina. A 40–59% decrease in the concentration of HFPO-DA was observed within 14 days for freshwater and estuarine sediments. This decrease could not be explained by biological degradation because there were no statistically significant differences in HFPO-DA loss between bioactive and autoclaved sediments and no degradation products were detected via high-resolution mass spectrometry. An additional 2–3% of HFPO-DA was recovered when sediments were subjected to a more aggressive extraction (12 h soak with 80:20 1 M NaOH in methanol/water), suggesting that HFPO-DA sorbs strongly to sediments and remains undetected by less aggressive PFAS sediment extraction methods. Results of this study highlight that (1) PFAS sediment extraction methodologies need to be re-evaluated, particularly as alternative compounds continue to be synthesized and discovered, and (2) studies employing less aggressive extraction methodologies significantly underestimate PFAS contamination in aquatic sediments. Given that HFPO-DA is resistant to biological degradation and has a high sorption affinity, aquatic sediments may be a more significant long-term sink for HFPO-DA and other short-chain alternative PFAS than previously thought.
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