Investigation of potential metal emissions from galvanic anodes in offshore wind farms into North Sea sediments.

To evaluate potential metal emissions from offshore wind farms (OWFs), 215 surface sediment samples from different German North Sea OWFs taken between 2016 and 2022 were analyzed for their mass fractions of metals and their isotopic composition of Sr. For the first time, this study provides large-scale elemental data from OWFs of the previously proposed galvanic anode tracers Cd, Pb, Zn, Ga and In. Results show that mass fractions of the legacy pollutants Cd, Pb and Zn were mostly within the known variability of North Sea sediments. At the current stage the analyzed Ga and In mass fractions as well as Ga/In ratios do not point towards an accumulation in sediments caused by galvanic anodes used in OWFs. However, further investigations are advisable to evaluate long-term effects over the expected lifetime of OWFs, especially with regard to the current intensification of offshore wind energy development.

Waste water treatment plants as sources of polyfluorinated compounds, polybrominated diphenyl ethers and musk fragrances to ambient air.

To investigate waste water treatment plants (WWTPs) as sources of polyfluorinated compounds (PFCs), polybrominated diphenyl ethers (PBDEs) and synthetic musk fragrances to the atmosphere, air samples were simultaneously taken at two WWTPs and two reference sites using high volume samplers. Contaminants were accumulated on glass fiber filters and PUF/XAD-2/PUF cartridges, extracted compound-dependent by MTBE/acetone, methanol, or hexane/acetone and detected by GC-MS or HPLC-MS/MS. Total (gas+particle phase) concentrations ranged from 97 to 1004 pg m(-3) (neutral PFCs),

Wet deposition of poly- and perfluorinated compounds in Northern Germany.

Twenty precipitation samples were taken concurrently with air samples at a northern German monitoring site over a period of 7 months in 2007 and 2008. Thirty four poly- and perfluorinated compounds (PFC) were determined in rain water samples by solid phase extraction and HPLC-MS/MS analysis. Seventeen compounds were detected in rain water with SigmaPFC concentrations ranging from 1.6 ng L(-1) to 48.6 ng L(-1). Perfluorooctanoate (PFOA) and perfluorobutanate (PFBA) were the compounds that were usually observed in highest concentrations. Calculated SigmaPFC deposition rates were between 2 and 91 ng m(-2) d(-1). These findings indicate that particle phase PFC are deposited from the atmosphere by precipitation. A relationship between PFC wet deposition and air concentration may be established via precipitation amounts. Trajectory analysis revealed that PFC concentration and deposition estimates in precipitation can only be explained if a detailed air mass history is considered.

Polyfluorinated compounds in the atmosphere of the Atlantic and Southern Oceans: evidence for a global distribution.

High volume air samples taken onboard several research vessels in the Atlantic Ocean, the Southern Ocean, and the Baltic Sea as well as at one land-based site close to Hamburg, Germany, in 2007 and 2008 were analyzed for per- and polyfluorinated organic compounds (PFCs). A set of neutral, volatile PFCs such as fluorotelomer alcohols (FTOH) or perfluoroalkyl sulfonamides and ionic nonvolatile PFCs like perfluorinated carboxylates (PFCA) and sulfonates (PFSA) were collected on PUF/XAD-2/PUF cartridges and glass fiber filters and determined using GC-MS and HPLC-MS/MS. PFCs were detected in all air samples, even in Antarctic regions, and occurred predominantly in the gas phase. Total gas-phase concentrations of ship-based samples ranged from 4.5 pg m(-3) in the Southern Ocean to 335 pg m(-3) in European source regions. Concentrations of 8:2 FTOH, the analyte that was usually observed in highest concentrations, were between 1.8 and 130 pg m(-3). PFC concentrations decreased from continental regions toward marine regions and from Central Europe toward the Arctic and Antarctica. Southern hemispheric concentrations of individual PFCs were significantly lower than those of the northern hemisphere. On the basis of this data set, marine background PFC concentrations and atmospheric residence times were calculated. This study gives further evidence that volatile PFCs undergo atmospheric long-range transportto remote regions and may contribute to their contamination with persistent PFCA and PFSA.