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首页> 外文期刊>Environmental Science & Technology >Subsurface Transport Potential of Perfluoroalkyl Acids at Aqueous Film-Forming Foam (AFFF)-Impacted Sites
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Subsurface Transport Potential of Perfluoroalkyl Acids at Aqueous Film-Forming Foam (AFFF)-Impacted Sites

机译:全氟烷基酸在水成膜泡沫(AFFF)撞击部位的地下运输潜力

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摘要

Subsurface transport potential of a suite of perfluoroalkyl acids (PFAAs) was studied in batch sorption experiments with various soils and in the presence of co-contaminants relevant to aqueous film-forming foam (AFFF)-impacted sites. Specifically, PFAA sorption to multiple soils in the presence of nonaqueous phase liquid (NAPL) and nonfluorinated AFFF surfactants was examined. This study is the first to report on sorption of perfluorobutanoate (PFBA) and perfluoropentanoate (PFPeA) (log K_∝=88 and 1.37, respectively) and found that sorption of these compounds does not follow the chain-length dependent trend observed for longer chain-length PFAAs. Sorption of PFBA was similar to that of perfluorooctanoate (PFOA, log _∝= 1.89). NAPL and nonfluorinated AFFF surfactants all had varying impacts on sorption of longer chain (>6 CF_2 groups) PFAAs. The primary impact of NAPL was observed in low f_∝soil (soil A) where Freundlich n-values increased when NAPL was present. Impacts of nonfluorinated AFFF surfactants varied with surfactant and soil. The anionic surfactant sodium decyl sulfate (SDS) illicited PFAA chain-length dependent impacts in two negatively charged soils with varying f_∝. In soil A, K_d values for perfluoroheptanoate (PFHpA) increased 91% with SDS, whereas values for perfluorodecanoate (PFDA) increased only 28%. An amphoteric surfactant, n,n-dimethyldodecylamine n-oxide (AO), had the most notable impact on PFAA sorption to a positively charged soil (soil C). In this soil, AO oxide significantly increased sorption for the longer chain PFAAs (i.e., 528% increase in K_d for PFDA). Changes in sorption caused by SDS and AO may be due to mixed hemimicelle formation, competitive sorption, or changes to PFAA solubility. Short-chain PFAA behavior in the presence of NAPL, SDS, and AO was again notable. Co-contaminants generally increased the sorption of these compounds to all soils. Log K_d values of PFBA in soil A increased 85%, 372%, and 32% in the presence of NAPL, SDS, and AO, respectively. Use of K_d values to calculate retardation factors (R_f) of PFAAs demonstrates the variability of co-contaminant impacts on PFAA transport. Whereas NAPL and nonfluorinated surfactants decreased the sorption of perfluorooctanesulfonate (PFOS) at lower PFOS concentrations (1 μg/L), they led to increases in sorption at higher PFOS concentrations (500 μg/L). These results demonstrate that PFAA groundwater transport will depend on the solid phase characteristics as well as PFAA concentration and chain length. Detailed site-specific information will likely be needed to accurately predict PFAA transport at AFFF-impacted sites.
机译:在批量吸附实验中,在各种土壤和存在与水成膜泡沫(AFFF)影响位点相关的共污染物质的条件下,对一组全氟烷基酸(PFAA)的地下运输潜力进行了研究。具体而言,研究了在非水相液体(NAPL)和非氟化AFFF表面活性剂存在下PFAA对多种土壤的吸附。这项研究是第一个报告全氟丁酸酯(PFBA)和全氟戊酸酯(PFPeA)的吸附(分别为log K_∝ = 88和1.37),并且发现这些化合物的吸附不遵循长链上观察到的链长依赖性趋势。长度的PFAA。 PFBA的吸附与全氟辛酸酯的吸附相似(PFOA,log ∝ = 1.89)。 NAPL和非氟化AFFF表面活性剂对更长链(> 6个CF_2基团)PFAA的吸附都有不同的影响。在低f土(土A)中观察到NAPL的主要影响,当存在NAPL时Freundlich n值增加。非氟化AFFF表面活性剂的影响随表面活性剂和土壤的不同而不同。阴离子表面活性剂癸基硫酸钠(SDS)在f_AA变化的两个带负电荷的土壤中对PFAA链长的影响取决于。在土壤A中,使用SDS的全氟庚酸(PFHpA)的K_d值增加91%,而全氟癸酸(PFDA)的K_d值仅增加28%。两性表面活性剂正氧化物n,n-二甲基十二烷基胺(AO)对PFAA吸附到带正电的土壤(土壤C)的影响最大。在这种土壤中,AO氧化物显着增加了较长链PFAAs的吸附(即,PFDA的K_d增加528%)。 SDS和AO引起的吸附变化可能是由于混合半胶束的形成,竞争性吸附或PFAA溶解度的变化。在存在NAPL,SDS和AO的情况下,短链PFAA行为再次显着。共污染物通常会增加这些化合物对所有土壤的吸附。在存在NAPL,SDS和AO的情况下,土壤A中PFBA的Log K_d值分别增加了85%,372%和32%。使用K_d值计算PFAAs的延迟因子(R_f)证明了共污染物对PFAA转运的影响的可变性。尽管NAPL和非氟化表面活性剂在较低的PFOS浓度(1μg/ L)下降低了全氟辛烷磺酸(PFOS)的吸附,但在较高的PFOS浓度(500μg/ L)下却导致了吸附的增加。这些结果表明,PFAA地下水的输送将取决于固相特征以及PFAA的浓度和链长。可能需要详细的特定地点信息,以准确预测受AFFF影响的地点的PFAA转运。

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  • 来源
    《Environmental Science & Technology》 |2013年第9期|4164-4171|共8页
  • 作者单位

    Department of Civil and Environmental Engineering, Colorado School of Mines, Golden, Colorado 80401, United States;

    Department of Civil and Environmental Engineering, Colorado School of Mines, Golden, Colorado 80401, United States;

  • 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
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