Occurrence and fate of legacy and novel per- and polyfluoroalkyl substances (PFASs) in freshwater after an industrial fire of unknown chemical stockpiles
- 1. School of Chemistry, Australian Laboratory for Emerging Contaminants, University of Melbourne, Victoria, 3010 (Australia)
- 2. MRC Centre for Environment and Health, Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London (United Kingdom)
- 3. School of BioSciences, University of Melbourne, Victoria, 3010 (Australia)
Description
Highlights: • Up to 42 PFASs were released into an 8 km fresh waterbody from an urban industrial fire. • ΣPFAS levels were up to 70X higher at the point-source than upstream sites. • 6:2 FTSA and PFOS were the dominant PFAS released downstream. • ΣPFAS concentrations decreased up to 98% after two years but were still 3–6X higher than upstream sites. • Emerging and novel PFASs were identified for the first time in the Australian environment. An industrial warehouse illegally storing a large quantity of unknown chemical and industrial waste ignited in an urban area in Melbourne, Australia. The multiday fire required firefighters to use large amounts of fluorine-free foam that carried contaminated firewater runoff into an adjacent freshwater creek. In this study, the occurrence and fate of 42 per- and polyfluoroalkyl substances (PFASs) was determined from triplicate surface water samples (n = 45) from five locations (upstream, point-source, downstream; 8 km) over three sampling campaigns from 2018 to 2020. Out of the 42 target PFASs, perfluorocarboxylates (PFCAs: C4–C14), perfluoroalkane sulfonates (PFSAs: C4–C10), and perfluoroalkyl acid precursors (e.g. 6:2 fluorotelomer sulfonate (6:2 FTSA)) were ubiquitously detected in surface waters (concentration ranges: p ≤ 0.001). The point-source ΣPFAS concentration decreased from 5500 ± 1200 ng/L to 960 ± 42 ng/L (−83%) after two months and to 430 ± 15 ng/L (−98%) two years later. 6:2 FTSA and perfluorooctanesulfonate (PFOS) dominated in surface water, representing on average 31% and 20% of the ΣPFAS, respectively. Emerging PFASs including a cyclic perfluoroalkanesulfonate (PFECHS) and a C4 perfluoroalkane sulfonamide (FBSA) were repeatedly present in surface water (concentration ranges <0.3–77 ng/L). According to the updated Australian PFAS guidelines for ecological conservation, the water samples collected at the time of monitoring may have posed a short-term risk to aquatic organisms in regard to PFOS levels. These results illustrate that acute high dose exposure to PFASs can result from industrial fires at sites storing or stockpiling PFAS-based waste products. Continued monitoring will be crucial to evaluate potential long-term risk to wildlife in the region.
Availability note (English)
Available from http://dx.doi.org/10.1016/j.envpol.2021.116839Additional details
Identifiers
- DOI
- 10.1016/j.envpol.2021.116839;
- PII
- S026974912100419X;
Publishing Information
- Journal Title
- Environmental Pollution (1987)
- Journal Volume
- 278
- Journal Page Range
- vp.
- ISSN
- 0269-7491
- CODEN
- ENPOEK
INIS
- Country of Publication
- United Kingdom
- Country of Input or Organization
- International Atomic Energy Agency (IAEA)
- INIS RN
- 54024332
- Subject category
- S54: ENVIRONMENTAL SCIENCES;
- Descriptors DEI
- AQUATIC ORGANISMS; CONCENTRATION RATIO; ECOLOGICAL CONCENTRATION; FLUORINE; FOAMS; FRESH WATER; INDUSTRIAL WASTES; POINT SOURCES; RECOMMENDATIONS; RUNOFF; SAMPLING; STREAMS; SULFONAMIDES; SULFONATES; URBAN AREAS; WILD ANIMALS
- Descriptors DEC
- AMIDES; ANIMALS; ANTI-INFECTIVE AGENTS; ANTIMICROBIAL AGENTS; COLLOIDS; DIMENSIONLESS NUMBERS; DISPERSIONS; DRUGS; ELEMENTS; ENVIRONMENTAL TRANSPORT; HALOGENS; HYDROGEN COMPOUNDS; MASS TRANSFER; NONMETALS; ORGANIC COMPOUNDS; ORGANIC NITROGEN COMPOUNDS; ORGANIC SULFUR COMPOUNDS; OXYGEN COMPOUNDS; RADIATION SOURCES; RIVERS; SURFACE WATERS; WASTES; WATER
Optional Information
- Copyright
- Copyright (c) 2021 Elsevier Ltd. All rights reserved.