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Subsurface transport potential of perfluoroalkyl acids (PFAAs): Column experiments and modeling

机译:全氟烷基酸(PFAAS)的地下传输电位:柱实验和建模

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摘要

Transport of ten perfluoroalkyl acids (PFAAs) was studied with one-dimensional (1-D) saturated column experiments using four soil types with an organic carbon fraction (f(oc)) range of similar to 0-0.045. Columns were operated under conditions relevant to aqueous film-forming foam (AFFF)-impacted fire protection training areas to determine the ability of equilibrium transport parameters to describe 1-D PFAA transport, if rate-limited sorption influences PFAA transport, and if kinetic parameters can be used to evaluate factors causing rate-limited sorption. Results of initial screening of PFAA breakthrough found that over half of the breakthrough curves deviated from equilibrium transport and merited further investigation. Subsequent analysis showed that, in many cases, these deviations could be accounted for by considering the range of applicable equilibrium K-d values (i.e. based on standard deviation) applicable to the solid phase. Thus, transport of the majority of PFAAs in 3 soils with f(oc) of 0-0.017 was not impacted by rate-limited sorption. Further, low sorption led to transport that was essentially simultaneous for the majority of PFAAs in these porous media. Exceptions were observed for long-chain PFAAs, and also in a fourth soil with f(oc) of 0.045, which indicated the potential for rate-limited sorption to impact transport in some scenarios. Subsequent flow interruption experiments isolating kinetic behavior confirmed rate-limited sorption caused nonequilibrium transport. Linear free energy relationships (LFERs) developed in previous work to predict the inverse relationship between mass transfer coefficients (k) and sorption parameters (i.e., K-d) were used to estimate values of k for PFAAs in this study. Resulting k values were 10(-3) to 10(-8) h(-1), consistent with previously measured kinetic parameters for other polar and anionic compounds. Models incorporating estimated k values resulted in improved predictions of breakthrough observed in nonequilibrium scenarios (R-2 0.83-0.98), but k values will require further validation prior to broader application. This work illustrates rate-limited sorption considerations are needed to describe 1-D column saturated transport for some PFAAs and solid phases. At field scales, subsurface heterogeneity and PFAA precursor transformation may be equally or even more important in determining saturated PFAA transport, but kinetic parameters in this study may help to determine relative contributions of rate-limited sorption to overall transport.
机译:使用四种土壤类型的一维(1-D)饱和柱实验研究了十个全氟烷基酸(PFAAs)的运输,其中有机碳馏分(F(OC))的相似与0-0.045。在与含水成膜泡沫(AFFF)的条件下进行柱式操作,用于确定平衡转运参数的能力,以描述1-D PFAA运输,如果速率限制吸附影响PFAA运输,以及动力学参数可用于评估导致速率有限吸附的因素。 PFAA突破的初始筛选结果发现,超过一半的突破性曲线偏离均衡运输并进行了进一步调查。随后的分析表明,在许多情况下,通过考虑适用的平衡K-D值(即,基于标准偏差),可以考虑适用于固相的范围来解决这些偏差。因此,在3个土壤中的大部分PFAAs的运输与0-0.017的F(OC)的速率有限吸附不受影响。此外,低吸附导致在这些多孔介质中基本上同时同时同时同时进行的运输。对于长链PFAAs观察到例外,并且还观察到具有0.045的F(OC)的第四种土壤,这表明在某些情况下影响运输的速率有限吸附。随后的流动中断实验分离动力学行为证实的速率限制吸附导致非QuiribriaM转运。在先前的工作中开发的线性自由能量关系(LFERS)以预测传质系数(k)和吸附参数(即,K-D)之间的反向关系用于估计本研究中PFAAs的K值。得到的k值为10(-3)至10(-8)H(-1),与预先测量的其他极性和阴离子化合物的动力学参数一致。结合估计的K值的模型导致在非识别情况下观察到的突破预测(R-2 0.83-0.98),但K值将需要在更广泛应用之前进行进一步的验证。该工作说明了对一些PFAAs和固相来描述1-D柱饱和转运所需的速率限制吸附考虑。在现场刻度,地下异质性和PFAA前体转化在确定饱和的PFAA运输时可以同样或更重要,但本研究中的动力学参数可能有助于确定对整体运输的限速吸附的相对贡献。

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  • 来源
    《Journal of Contaminant Hydrology》 |2020年第8期|103661.1-103661.9|共9页
  • 作者单位

    Texas Tech Univ Dept Civil Environm & Construct Engn Box 41023 Lubbock TX 79409 USA|Colorado Sch Mines Dept Civil & Environm Engn 1500 Illinois St Golden CO 80401 USA;

    Colorado Sch Mines Dept Civil & Environm Engn 1500 Illinois St Golden CO 80401 USA;

    Colorado Sch Mines Dept Civil & Environm Engn 1500 Illinois St Golden CO 80401 USA;

    Colorado Sch Mines Dept Civil & Environm Engn 1500 Illinois St Golden CO 80401 USA;

    Colorado Sch Mines Dept Civil & Environm Engn 1500 Illinois St Golden CO 80401 USA;

  • 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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  • 正文语种 eng
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