Environmental Science Department, The University of Arizona, Tucson, AZ, 85721, United States; Hydrology and Atmospheric Sciences Department, The University of Arizona, Tucson, AZ, 85721, United States.
Hydrology and Atmospheric Sciences Department, The University of Arizona, Tucson, AZ, 85721, United States.
Chemosphere. 2022 Sep;302:134938. doi: 10.1016/j.chemosphere.2022.134938. Epub 2022 May 11.
Determining the risk posed by PFAS leaching from soil to groundwater requires quantification of the magnitude and temporal/spatial variability of PFAS mass discharge from the vadose zone, which is governed in part by the concentrations of PFAS in soil porewater. Porewater concentrations are impacted and mediated by the properties of the PFAS and soil, multiple transport and fate processes, and site conditions. The objective of this research was to delineate the relationship between soil porewater concentrations and soil concentrations, based on a comprehensive model of PFAS mass distribution within a soil sample volume. Measured parameters representing solid-phase sorption and air-water interfacial adsorption are used to illustrate the impact of soil and PFAS properties on the distribution of representative PFAS between soil and soil porewater. Literature data reported for soil and soil porewater concentrations of several PFAS obtained from outdoor lysimeter experiments are used to test the distribution model. Soil-to-porewater concentration ratios predicted with the model compared very well to the measured concentration ratios. The nondimensional distribution coefficient that describes the distribution of PFAS mass amongst all domains within a soil sample was observed to be a function of PFAS molecular size. Numerical simulations conducted for a model fire-training source area were used to illustrate the ranges in magnitude of soil versus porewater concentrations for representative field conditions. The results of the measured and simulated data sets demonstrated the importance of air-water interfacial adsorption for the distribution of the longer-chain PFAS within soil samples. PFAS soil porewater concentrations are anticipated to range from ng/L to mg/L depending upon soil concentrations, which in turn depend upon the nature of the site.
确定 PFAS 从土壤向地下水浸出所带来的风险,需要量化从包气带中 PFAS 质量排放量的大小和时空变异性,这部分受到土壤孔隙水中 PFAS 浓度的控制。土壤孔隙水中的浓度受到 PFAS 和土壤特性、多种传输和归宿过程以及场地条件的影响和调节。本研究的目的是基于 PFAS 在土壤样品体积内的质量分布综合模型,阐明土壤孔隙水浓度与土壤浓度之间的关系。测量的参数代表固相吸附和气-水界面吸附,用于说明土壤和 PFAS 特性对代表性 PFAS 在土壤和土壤孔隙水之间分布的影响。使用从户外淋溶实验中获得的几种 PFAS 的土壤和土壤孔隙水浓度的文献数据来测试分配模型。模型预测的土壤-孔隙水浓度比与实测浓度比非常吻合。描述 PFAS 质量在土壤样品内所有区域之间分配的无量纲分配系数被观察为 PFAS 分子大小的函数。针对模型火灾训练源区进行的数值模拟用于说明代表现场条件的土壤与孔隙水中浓度的幅度范围。实测和模拟数据集的结果表明,气-水界面吸附对土壤样品中长链 PFAS 的分布具有重要影响。PFAS 土壤孔隙水浓度预计在 ng/L 到 mg/L 之间变化,具体取决于土壤浓度,而土壤浓度又取决于场地的性质。