Abstract

This study evaluates the effectiveness of non-thermal plasma at atmospheric pressure (NTP APPJ) for treating PFAS - contaminated water in different matrices. Successful removal of several perfluoroalkyl carboxylic acids (PFCAs) (C6 to C4), perfluroalkane sulfonic acids (PFSAs) (C8 to C4) and perfluropolyethers (PFPEs) (GenX and ADONA) PFAS compounds was achieved in laboratory scale experiments. In the deionized water (DW), high removal efficiencies (> 90%) were observed for longer-chain PFAS, PFOS (99.89%), PFHxA (94.61%) and ADONA (94.83%), while shorter- chain compounds had lower removal rates. Real water samples (tap water and synthetic effluent) showed lower overall degradation percentages (8–50%) depending on compound and matrix. Short-chain PFAS displayed around 10% removal in tap water, while PFOS and GenX achieved 50% and 32% removal, respectively. Complex matrix effects influence degradation rates. Byproducts from the plasma treatment were investigated, revealing distinct degradation mechanisms for various PFAS compounds. For PFSAs and PFCAs, degradation involved electron transfer, bond breaking and subsequent reactions. Conversely, ADONA and GenX degradation initiated with ether-group cleavage, followed by additional transformation processes. Plasma-based technology shows potential for degradation of PFAS, especially for newer substitute compounds like ADONA and GenX. However, further research is needed to optimize plasma performance for complete mineralization of PFAS. This study also proposes a degradation mechanism for ADONA, marking a novel investigation into ether-group PFAS degradation with potential implications for further research and understanding toxicological implications.

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