Lower Critical Solution Temperature-Driven Catch and Release of Perfluoroalkyl Substances from Water: Remediation and Sampling AITranslate

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DOI：https://doi.org/10.1021/acsapm.1c00608

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Water pollution by per- and polyfluoroalkyl substances (PFASs) is a rising issue for the environment and human health because PFASs are persistent and nonbiodegradable. Recent studies have revealed that the concentration of PFASs found in contaminated water is in the order of the parts per trillion (i.e., 10–12) scale. This can result in a grand challenge for scientists not only to remove PFASs from water but to detect them. Various methodologies including functionalized nanoparticles, bioassay, activated carbon, anion exchange resin, and molecularly imprinted polymers have been employed to detect or remove PFASs from water. Dynamic adsorbents have demonstrated that they can adsorb PFASs from water while releasing them on demand for reuse upon an external trigger. This enables one to remove PFASs from water and retain them for preconcentration, while on-demand releasing allows for regenerating the adsorbent for reuse. Herein, a poly(isopropylmethacrylamide) (P-NIPMAM)-based adsorbent that can adsorb and retain PFASs at a temperature higher than its lower critical solution temperature (LCST) while releasing them at a lower temperature is reported. Perfluorooctanoic acid (PFOA) and perfluorohexanoic acid (i.e., PFHxA) are utilized as a representative PFAS with a long and short fluoroalkyl chain, respectively. The adsorption capacity for PFOA and PFHxA is measured as ≈37 and ≈18 mg g–1 at 75 °C, respectively. When the adsorbent is submerged in water at a lower temperature (e.g., 23 °C < LCST), it starts to release the adsorbed compounds resulting in the desorption efficiency of ≈0.66 and ≈0.81 for PFOA and PFHxA, respectively. Finally, a prototype PFAS sampler was engineered by utilizing P-NIPMAM that can demonstrate the LCST-driven reversible adsorption and desorption of PFASs.