Legacy and emerging poly- and perfluorochemicals in seawater and sediment from East China Sea.

Following the global phase out of perfluorooctane sulfate (PFOS), chlorinated polyfluoroalkyl ether sulfonates (Cl-PFAESs) and p-perfluorous nonenoxybenzenesulfonate (PFNOBS) have emerged as novel PFOS substitutes. However, until now, limited data is available on their occurrence and environmental behaviors in the marine environment. Here, seawater and sediment samples were collected from East China Sea and analyzed for Cl-PFAESs, PFNOBS, and perfluoroalkyl acids (PFAAs; including their branched isomers) to investigate their concentrations, potential sources, and sediment-seawater partitioning behaviors. Perfluorooctanoate (PFOA) and PFOS were consistently the predominant PFAAs in seawaters and sediments. Branched PFOA and PFOS isomers were consistently much less frequently detected in sediments than that in seawaters. Linear PFOA contributed 92-95% of total PFOA in seawaters, suggesting the great contribution of telomerization PFOA. 6:2 Cl-PFAES was detected in all seawaters (concentration, 0.58-47 pg/L) and in the majority of sediments (<LOD-28 pg/g). PFNOBS was observed in 46% of seawater samples (concentration, <LOD-5.2 pg/L) and 66% of sediment samples (<LOD-1.7 pg/g). Spatial distribution trend suggested the riverine input as an important source of PFAAs and 6:2 Cl-PFAES in this sampling area. 6:2 Cl-PFAES (log K, 2.6 ± 0.36) and PFNOBS (2.7 ± 0.33) had comparable mean log-transformed sediment-seawater partitioning coefficients (log K) to PFOA (2.5 ± 0.32) or PFOS (2.8 ± 0.49), indicating their long-range transport potential in global oceans with ocean currents. Overall, this study provides the first data on occurrence and partitioning behaviors of 6:2 Cl-PFAES and PFNOBS in the marine environment.