摘要
Anion exchange resin (AER) adsorption is an effective technology for removing per- and polyfluoroalkyl substances (PFAS) from drinking water. However, conventional AERs exhibit poor adsorption selectivity, and the adsorption differences among different amine functional groups for low-concentration PFAS in drinking water remain unclear. In this study, multiple AERs with different amine groups were synthesized, and the structure-selectivity relationship of AERs for PFAS adsorption was revealed through competitive adsorption experiments. It was found that AERs with hydrophobic long alkyl chains, strong-base quaternary amine groups, and gel-type pore structures demonstrated higher adsorption selectivity for PFAS. Furthermore, the removal efficiency of low-concentration PFAS in drinking water by AERs was highly correlated with adsorption selectivity. Based on these findings, a synthesized gel-type strong-base AER with long alkyl chains (Gel(12-1-1)) was selected as the optimal AER, and its adsorption performance for PFAS in drinking water was evaluated through rapid small-scale column tests (RSSCTs). During the treatment of 180,000 bed volumes (BV), the effluent concentrations of PFBS, PFHxS, PFOS, PFOA, PFNA and GenX consistently remained below 10 ng/L. If targeting the U.S. drinking water regulatory limit of 4 ng/L for PFOS and PFOA, the commercial resin PFA694E could only treat 42,000 BV of water, whereas Gel(12-1-1) could treat 97,000 BV, demonstrating a significant advantage. This study not only provides an efficient and practical material for PFAS adsorption from drinking water, but also establishes a theoretical basis for the selective and ultimate removal of low-concentration PFAS.
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