Zwitterionic, cationic, and anionic PFAS in freshwater sediments from AFFF-impacted and non-impacted sites of Eastern Canada

Abstract

Zwitterionic, cationic, and anionic per- and polyfluoroalkyl substances (PFAS) were investigated in freshwater sediments of Canada, including sites impacted by aqueous film-forming foams (AFFFs). The first step of the project involved optimizing the extraction method with equilibrated sediment-water-AFFF samples. The analytical method had acceptable linearity, accuracy, and precision in the sediment matrix, and was further validated with NIST SRM 1936. In the second step of the project, the method was applied to determine over 70 target PFAS in field-collected sediments (n = 102). At federal contaminated sites of Ontario, Newfoundland, and Québec (ditches and creeks at international airports with fire training or fire equipment testing areas), summed PFAS averaged 30 ng/g (max of 160 ng/g) with molecular patterns dominated by perfluorooctane sulfonate (maximum PFOS: 84 ng/g). Based on maximum observed concentrations >10 ng/g, other key PFAS at these AFFF-impacted sites included negative ion mode perfluorohexane sulfonate, perfluorohexane sulfonamide, fluorotelomer sulfonates (6:2 FTS and 8:2 FTS) and 5:3 fluorotelomer acid, and positive ion mode N-dimethylammoniopropyl perfluorohexane sulfonamide and 5:1:2 fluorotelomer betaine. In contrast, environmental sediment samples collected at a larger spatial scale (province-wide survey) were characterized by low ΣPFAS (generally <1 ng/g), with PFOS/PFOA below chronic toxicity thresholds for aquatic life.