Advanced oxidation processes may transform unknown PFAS in groundwater into known products.

Per- and polyfluoroalkyl substances (PFAS) are a group of fluorinated organic contaminants classified as persistent in the aquatic environment. Early studies using targeted analysis approaches to evaluate the degradation of PFAS by advanced oxidation processes (AOP) in real water matrices may have been misinterpreted due to the presence of undetected or unknown PFAS in these matrices. The aims of the present study were to (1) screen selected commercially available AOPs (UV, UV + H2O2, O3/H2O2) and UV photocatalysis in a pilot system using commercially used and novel photocatalysts (TiO2, boron nitride [BN]) for removing PFAS contaminants and (2) evaluate their role on the conversion of non-detected/unknown to known PFAS compounds in real groundwater used as drinking water supplies. Results indicated that, while AOPs have the potential to achieve removal of the EPA method 533 target PFAS compounds (PFDA [100%], PFNA [100%], PFOA [85-94%], PFOS [25-100%], PFHxS [3-100%], PFPeS [100%], PFBS [100%]), AOPs transformed non-detected/unknown longer-chain PFAS compounds to detectable shorter-chain ones under very high-dose AOP operating conditions, leading to an increase in ∑PFAS concentration ranging from 95% to 340%. As emerging PFAS treatment processes transition from lab-scale investigations of target PFAS to pilot testing of real water matrices, studies will need to consider impact of the presence of non-target long-chain PFAS to transform into targeted PFAS compounds. A promising approach to address the potential risks and unforeseen consequences could involve an increased reliance on adsorbable organic fluorine (AOF) analysis before and after advanced oxidation process (AOP) treatment.

Petroleum hydrocarbon contamination of the Southern Black Sea Shelf, Turkey.

INTRODUCTION: In this study, total petroleum hydrocarbon (TPH) contents and some aliphatic and aromatic hydrocarbon concentrations were analysed in coastal sediments of hot points collected from along the Southern Black Sea Shelf. MATERIALS AND METHODS: Surface sediment (0-2 cm) samples were collected from the locations using a Van Veen type grab sampler in September 2008 during a cruise on the Pollution Monitoring R/V ARAR. All sampling procedures were carried out according to internationally recognized guide-lines (UNEP 1991). Samples were analysed using a UV-fluorescence spec-trophotometry (UNEP/IOC/IAEA 1992) and gas chromatog- raphy (GC) via a Hewlett-Packard HP6890N series with a selective detector (GC-MSD) after hexane/ dichloromethane extraction. RESULTS AND DISCUSSION: The ratio C(17)/C(18) varied between 2.2 and 2.9 for the surface sediments of TRK 34Y (Samsun), TRK46 (Giresun), and TRK55 (Rize), respectively. These results showed higher marine organic matter accumulation. However, pyrolytic PAHs were found predominant in these areas. In contrast, petrogenic contributions were found at Stations TRK1 (Igneada), TRK13 (Zonguldak), TRK53 (Trabzon) and TRK61 (Hopa). TPH contents of surface sediments varied between 0.29 and 363 µg g(-1) (dry wt) throughout the shelf. The lowest values were measured at Stations TRK1 (Igneada) and TRK 19 (Bartin), whereas the highest values were found at Stations TRK13 (Zonguldak) and TRK 53 (Trabzon).