Your browser doesn't support javascript.
loading
Fast analysis of short-chain and ultra-short-chain fluorinated organics in water by on-line extraction coupled to HPLC-HRMS.
Wang, Yu; Liu, Min; Vo Duy, Sung; Munoz, Gabriel; Sauvé, Sébastien; Liu, Jinxia.
Afiliação
  • Wang Y; Department of Civil Engineering, McGill University, Montreal, QC H3A 0C3, Canada.
  • Liu M; Department of Civil Engineering, McGill University, Montreal, QC H3A 0C3, Canada; Department of Chemistry, Université de Montréal, Montreal, QC H2V 0B3, Canada.
  • Vo Duy S; Department of Chemistry, Université de Montréal, Montreal, QC H2V 0B3, Canada; Centre d'expertise en analyse environnementale du Québec, Ministère de l'Environnement, de la Lutte contre les changements climatiques, de la Faune et des Parcs, Québec, QC G1P 3W8, Canada.
  • Munoz G; Department of Chemistry, Université de Montréal, Montreal, QC H2V 0B3, Canada; Centre d'expertise en analyse environnementale du Québec, Ministère de l'Environnement, de la Lutte contre les changements climatiques, de la Faune et des Parcs, Québec, QC G1P 3W8, Canada.
  • Sauvé S; Department of Chemistry, Université de Montréal, Montreal, QC H2V 0B3, Canada.
  • Liu J; Department of Civil Engineering, McGill University, Montreal, QC H3A 0C3, Canada. Electronic address: jinxia.liu@mcgill.ca.
Sci Total Environ ; 943: 173682, 2024 Sep 15.
Article em En | MEDLINE | ID: mdl-38825196
ABSTRACT
A rapid on-line solid-phase extraction liquid chromatography high-resolution mass spectrometry (on-line SPE-LC-HRMS) method was developed to analyze 11 ultra-short and short-chain PFAS in surface water. Analytical optimization involved screening 7 chromatographic columns and 5 on-line SPE columns, as well as evaluating SPE loading conditions, filters, sample acidification, chromatographic mobile phases, and SPE loading mobile phases. The optimized method was then applied to 44 river water samples collected in Eastern Canada, including sites near airports with fire-training areas. Among the 11 targeted PFAS, the most frequently detected were trifluoroacetic acid (TFA, 4.6-220 ng/L), perfluorobutanoic acid (PFBA, 0.85-33 ng/L), perfluoropentanoic acid (PFPeA, 1.2-2100 ng/L), trifluoromethane sulfonic acid (TMS, 0.01-4.3 ng/L), and perfluorobutane sulfonic acid (PFBS, 0.07-450 ng/L). Levels of C3-C5 perfluoroalkyl carboxylic acids (PFCAs), C2-C4 perfluoroalkyl sulfonates (PFSAs) and n3 polyfluoroalkyl acids (n = 2,3; n3 acids) were significantly higher in water bodies near fire-training area sites compared with rivers in urban areas. In contrast, TFA, TMS, and 13 acid were not significantly elevated, likely reflecting atmospheric deposition or other diffuse sources for these compounds. Nontarget and suspect screening analysis revealed an abundance of other ultra-short and short-chain PFAS in AFFF-impacted water bodies. Perfluoroalkyl sulfonamides (FASA, C2, C3, and C5), perfluoroalkyl sulfonamide propanoic acids (FASA-PrA, C1-C2) and n3 acids (n = 1, 4, and 5) were detected for the first time in environmental surface waters.
Palavras-chave

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sci Total Environ Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá País de publicação: Holanda

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Sci Total Environ Ano de publicação: 2024 Tipo de documento: Article País de afiliação: Canadá País de publicação: Holanda