Transport of bisphenol A, bisphenol S, and three bisphenol F isomers in saturated soils

With the limitation of the use of bisphenol A (BPA), the production of its substitutes, bisphenol S (BPS), and bisphenol F (4,4'-BPF) is increasing. Understanding the fate and transport of BPA and its substitutes in porous media can help reduce their risk of contaminating soil and groundwater systems. In this study, column and batch adsorption experiments were performed with ¹⁴C-labeled bisphenol analogs and combined with mathematical models to investigate the interaction of BPA, BPS, 4,4'-BPF, 2,2'-BPF, and 2,4'-BPF with four standard soils with different soil organic matter (SOM) contents. The results show that the transport capacity of BPS and 4,4'-BPF in the saturated soils is significantly stronger than that of BPA. Meanwhile, the mobility of the three isomers of bisphenol F exhibits variability in saturated soils with high SOM content. The two-site nonequilibrium sorption model was applied to simulate and interpret column experimental data, and model simulations described the interactions between the bisphenol analogs and soil very well. The fitting results underscore SOM's role in providing dynamic adsorption sites for bisphenol analogs. Hydrophobicity primarily accounts for the disparity in adsorption affinity between BPA, BPS, 4,4'-BPF, and soil, whereas hydrogen bonding forces may predominantly influence the differential adsorption affinity between 4,4'-BPF and its isomers and soil. The results of this study indicate that BPS and three isomers of BPF, as alternatives to BPA, have higher mobility in saturated soils and may pose a substantial risk to groundwater quality. This study enhances our understanding of bisphenol analogs' behavior in natural soils, facilitating an assessment of their environmental implications, particularly regarding groundwater contamination.