Non-conventional sorption materials for the removal of legacy and emerging PFAS from water: A review

Per- and polyfluoroalkyl substances (PFAS) are a class of ubiquitous, persistent, and hazardous pollutants that raise concerns for human health and the environment. Typically, PFAS removal from water relies on adsorption techniques using conventional sorption materials like activated carbons (ACs) and ion exchange resins (IERs). However, there is a continuous search for more efficient and performing adsorbent materials to better address the wide range of chemical structures of PFAS in the environment, to increase their selectivity, and to achieve an overall high adsorption capacity and faster uptake kinetics. In this context, results from the application of non-conventional sorption materials (i.e., readily available biological-based materials like proteins and advanced materials like nanocomposites and cyclodextrins) are reported and discussed in consideration of the following criteria: i) removal efficiency and kinetics of legacy PFAS (e.g., PFOA, PFBA) as well as newly-introduced and emerging PFAS (e.g., GenX), ii) representativity of environmental conditions in the experimental setup (e.g., use of environmentally relevant experimental concentrations), iii) regenerability, reusability and applicability of the materials, and iv) role of the material modifications on PFAS adsorption. From this review, it emerged that organic frameworks, nano(ligno)cellulosic-based materials, and layered double hydroxides are among the most promising materials herein investigated for PFAS adsorption, and it was also observed that the presence of fluorine- and amine-moieties in the material structure improve both the selectivity and PFAS uptake. However, the lack of data on their applicability in real environments and the costs involved means that this research is still in its infancy and need further investigation. (c) 2024 The Authors. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co. Ltd. This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/ 4.0/).