Cited by 54Per- and polyfluoroalkyl substances researchUrban Stormwater Management SolutionsPharmaceutical and Antibiotic Environmental Impacts

Fate and transport of perfluoro- and polyfluoroalkyl substances including perfluorooctane sulfonamides in a managed urban water body

Nguyen, Tung V., Reinhard, Martin, Chen, Huiting, Gin, Karina Y.-H.·2016·Environmental Science and Pollution Research

Abstract

Transport and fate of perfluoro- and polyfluoroalkyl substances (PFASs) in an urban water body that receives mainly urban runoff was investigated. Water, suspended solids, and sediment samples were collected during the monsoon (wet) and inter-monsoon (dry) season at different sites and depths. Samples were analyzed for C7 to C12 perfluoroalkyl carboxylate homologues (PFCAs) (PFHpA, PFOA, PFNA, PFDA, PFUnA, PFDoA), perfluorohexane, perfluorooctane, and 6:2-fluorotelomer sulfonate (PFHxS, PFOS, and 6:2FtS, respectively), perfluorooctane sulfonamide (FOSA), N-ethyl FOSA (sulfluramid), N-ethyl sulfonamidoethanol (N-EtFOSE), and N-methyl and N-ethyl sulfonamidoacetic acid (N-EtFOSAA and N-MeFOSAA, respectively). Concentrations in wet samples were only slightly higher. The sum total PFAS (ΣPFAS) concentrations dissolved in the aqueous phase and sorbed to suspended solids (SS) ranged from 107 to 253 ng/L and 11 to 158 ng/L, respectively. PFOA, PFOS, PFNA, PFHxS, and PFDA contributed most (approximately 90 %) to the dissolved ΣPFASs. N-EtFOSA dominated the particulate PFAS burden in wet samples. K D values of PFOA and PFOS calculated from paired SS and water concentrations varied widely (1.4 to 13.7 and 1.9 to 98.9 for PFOA and PFOS, respectively). Field derived K D was significantly higher than laboratory K D suggesting hydrophobic PFASs sorbed to SS resist desorption. The ΣPFAS concentrations in the top sedimentary layer ranged from 8 to 42 μg/kg and indicated preferential accumulation of the strongly sorbing long-chain PFASs. The occurrence of the metabolites N-MeFOSAA, N-EtFOSAA and FOSA in the water column and sediments may have resulted from biological or photochemical transformations of perfluorooctane sulfonamide precursors while the absence of FOSA, N-EtFOSA and 6:2FtS in sediments was consistent with biotransformation.

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Crossref · 10.1007/s11356-016-6788-9

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Authors
Nguyen, T. V., Reinhard, M., Chen, H., & Gin, K. Y.-H.
Affiliations
  • Public Utilities Board (SG)
  • National University of Singapore (SG)
Corresponding author
Reinhard, Martin
Venue
Environmental Science and Pollution Research
Published
2016-05-05
Volume
23
Issue
11
Pages
10382-10392
ISSN
  • 0944-1344 (ISSN-L)
  • 1614-7499
OpenAlex
W2345657146
Cited by
54
References
11
Citations by year
2026: 6 · 2025: 6 · 2024: 9 · 2023: 2 · 2022: 7 · 2021: 10 · 2020: 2 · 2019: 3 · 2018: 4 · 2017: 5
FWCI
2.61
Type
journal article
Language
en
Open access
closed
Locations
  • Environmental Science and Pollution Research (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • National Research Foundation Singapore (SG)
  • Campus for Research Excellence and Technological Enterprise (CREATE) program
Topics
  • Physical Sciences › Environmental Science › Environmental Chemistry › Per- and polyfluoroalkyl substances research
  • Physical Sciences › Environmental Science › Environmental Engineering › Urban Stormwater Management Solutions
  • Physical Sciences › Environmental Science › Pollution › Pharmaceutical and Antibiotic Environmental Impacts
Keywords
PFAS fate and transport, urban runoff, perfluorooctanoic acid, PFOS, sediment sorption, suspended solids, seasonal variation, monsoon, PFAS degradation
MeSH terms
Biotransformation, Environmental Monitoring, Fluorocarbons, Hydrocarbons, Fluorinated, Singapore, Sulfonamides, Water Pollutants, Chemical, Water Supply, Alkanesulfonic Acids, Geologic Sediments

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