Per- and Polyfluoroalkyl Substances (PFAS) are anthropogenic chemicals consisting of thousands of individual species. PFAS consists of a fully or partly fluorinated carbon–fluorine bond, which is hard to break and requires a high amount of energy (536 kJ/mole). Resulting from their unique hydrophobic/oleophobic nature and their chemical and mechanical stability, they are highly resistant to thermal, chemical, and biological degradation. PFAS have been used extensively worldwide since the 1940s in various products such as non-stick household items, food-packaging, cosmetics, electronics, and firefighting foams. Exposure to PFAS may lead to health issues such as hormonal imbalances, a compromised immune system, cancer, fertility disorders, and adverse effects on fetal growth and learning ability in children. To date, very few novel membrane approaches have been reported effective in removing and destroying PFAS. Therefore, this article provides a critical review of PFAS treatment and removal approaches by membrane separation systems. We discuss recently reported novel and effective membrane techniques for PFAS separation and include a detailed discussion of parameters affecting PFAS membrane separation and destruction. Moreover, an estimation of cost analysis is also included for each treatment technology. Additionally, since the PFAS treatment technology is still growing, we have incorporated several future directions for efficient PFAS treatment.

Drinking water contamination by per- and polyfluorinated alkyl substances (PFAS) is a global concern. Nanofiltration is a promising PFAS removal technology due to its scalability and cost-effectiveness. However, nanofiltration cannot typically reduce PFAS concentrations below current drinking water recommendations. To enhance PFAS removal, we developed mixed-matrix-composite nanofiltration (MMCNF) membranes—an active nanofiltration layer on porous adsorptive support that synergetically combines filtration and adsorption. We synthesized MMCNF membranes comprising thin polyelectrolyte multilayer films deposited on thick (~400 µm) polyethersulfone supports incorporating β-cyclodextrin microparticles. These membranes achieved near complete removal (>99.9%) of model PFAS (PFOA: perfluorooctanoic acid) for significantly longer filtration times compared to a control membrane without β-cyclodextrin, but otherwise identical. The spent MMCNF membrane was regenerated using ethanol, and high PFOA removal performance was regained during three filtration cycles. Perfluorooctanoic acid was concentrated 38-fold in the ethanol eluent. Further concentration by evaporation is straightforward and can enable eluent recycling and effective PFAS removal.