Environmental Science Department, University of Arizona, Tucson, AZ 85721, USA.
Department of Plant & Environmental Science, New Mexico State University, Las Cruces, NM 88003, USA; Water Science and Management Program, New Mexico State University, Las Cruces, NM 88003, USA.
Sci Total Environ. 2021 Jul 20;779:146444. doi: 10.1016/j.scitotenv.2021.146444. Epub 2021 Mar 13.
The objectives of this research were to examine the transport of perfluorooctane sulfonic acid (PFOS) in aquifer sediment comprising different geochemical properties, and to compare the behavior to that observed for PFOS transport in soil and sand. PFOS retardation was relatively low for transport in all aquifer media. The PFOS breakthrough curves were asymmetrical and exhibited extensive concentration tailing, indicating that sorption/desorption was significantly nonideal. The results of model simulations indicated that rate-limited sorption/desorption was the primary cause of the nonideal PFOS transport. Comparison of PFOS transport in aquifer media to data reported for PFOS transport in two soils and a quartz sand showed that PFOS exhibited more extensive elution tailing for the soils, likely reflecting differences in the relative contributions of various media constituents to sorption. A three-component distributed-sorption model was developed that accounted for contributions from soil organic carbon, metal oxides, and silt + clay fraction. The model produced very good predictions of K for the five media with lower soil organic‑carbon contents (≤0.1%). Soil organic carbon was estimated to contribute 19-42% of the total sorption for all media except the sand, to which it contributed ~100%. The contribution of silt + clay ranged from 51 to 80% for all media except the sand. The only medium for which the contribution of metal-oxides was significant is Hanford, with an estimated contribution of 15%. Overall, the results of the study indicate that sorption of PFOS by these aquifer media comprised contributions from multiple soil constituents.
本研究的目的是考察在具有不同地球化学性质的含水层沉积物中,全氟辛烷磺酸(PFOS)的运移情况,并将其与在土壤和砂中观察到的 PFOS 运移行为进行比较。在所有含水层介质中,PFOS 的阻滞作用都相对较低。PFOS 的穿透曲线不对称,表现出广泛的浓度拖尾,表明吸附/解吸显著非理想。模型模拟结果表明,速率限制的吸附/解吸是 PFOS 非理想运移的主要原因。将含水层介质中 PFOS 的运移与两种土壤和石英砂中 PFOS 运移的数据进行比较表明,PFOS 在土壤中表现出更广泛的洗脱拖尾,这可能反映了不同介质成分对吸附的相对贡献的差异。开发了一个三组分分布吸附模型,该模型考虑了土壤有机碳、金属氧化物和粉土+粘土部分的贡献。该模型对五种土壤有机碳含量较低(≤0.1%)的介质的 K 值进行了很好的预测。土壤有机碳估计对所有介质(除砂外)的总吸附贡献了 19-42%,而对砂的贡献约为 100%。除砂外,粉土+粘土对所有介质的贡献范围为 51-80%。唯一对金属氧化物贡献显著的介质是汉福德,估计贡献为 15%。总的来说,研究结果表明,这些含水层介质对 PFOS 的吸附包括多种土壤成分的贡献。