Examining the robustness and concentration dependency of PFAS air-water and NAPL-water interfacial adsorption coefficients

表面张力 吸附 化学 吉布斯等温线 地表水 肺表面活性物质 热力学 分析化学(期刊) 环境化学 环境科学 环境工程 物理 物理化学 生物化学
作者
Mark L. Brusseau
出处
期刊:Water Research [Elsevier BV]
卷期号:190: 116778-116778 被引量:43
标识
DOI:10.1016/j.watres.2020.116778
摘要

Determining robust values for the air-water or NAPL-water interfacial adsorption coefficient, KIA, is key to characterizing and modeling PFAS transport and fate in several environmental systems. Direct, high-resolution measurements of surfactant adsorption at the fluid-fluid interface were aggregated from the literature. This data set was used to examine the accuracy and applicability of Γ and KIA measurements determined for three PFAS from transport experiments and surface-tension data. The transport-measured Γ and KIA data were observed to be fully consistent with the directly-measured data. Specifically, Γ values for the two methods were entirely coincident in the region of overlapping concentrations, which spanned ~4 orders-of-magnitude. Furthermore, the two data sets adhered to an identical Γ-C profile. These results conclusively demonstrate the accuracy of the transport-measured values. Γ and KIA values determined from the application of the Gibbs adsorption equation to measured surface-tension data were fully consistent with the directly-measured and transport-measured data sets, demonstrating their applicability for representing PFAS transport in environmental systems. The directly-measured data were used to examine the concentration dependency of KIA values, absent the potential confounding effects associated with the use of surface-tension or transport-measured data. The directly-measured data clearly demonstrate that KIA attains a constant, maximum limit at lower concentrations. Two separate analyses of the transport-measured data both produced observations of constant KIA values at lower concentrations, consistent with the directly-measured data. These outcomes are discussed in terms of surface activities, relative surface coverages, and critical concentrations.
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