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Nonderivatized Method for the Detection of Perfluoroalkane Sulfonyl Fluorides by Liquid Chromatography-Microwave Plasma Torch Ionization Mass Spectrometry.
Chu, Fengjian; Wei, Wei; Zhao, Gaosheng; Zhu, Junchen; Sun, Cuirong; Pan, Yuanjiang; Wang, Xiaozhi; Feng, Hongru.
Affiliation
  • Chu F; Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang, China.
  • Wei W; College of Information Science and Electronic Engineering, Zhejiang University, Hangzhou 310027, Zhejiang, China.
  • Zhao G; Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang, China.
  • Zhu J; School of Environmental and Chemical Engineering, Shanghai University, Shanghai 200444, China.
  • Sun C; Key Laboratory of Advanced Drug Delivery Systems of Zhejiang Province, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, Zhejiang, China.
  • Pan Y; Key Laboratory of Advanced Drug Delivery Systems of Zhejiang Province, College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, Zhejiang, China.
  • Wang X; Department of Chemistry, Zhejiang University, Hangzhou 310027, Zhejiang, China.
  • Feng H; College of Information Science and Electronic Engineering, Zhejiang University, Hangzhou 310027, Zhejiang, China.
Anal Chem ; 96(14): 5664-5668, 2024 Apr 09.
Article in En | MEDLINE | ID: mdl-38530953
ABSTRACT
Per- and polyfluoroalkyl substances (PFAS) have caused widespread environmental concern in recent years. Among them, the levels of perfluoroalkane sulfonyl fluorides (PFASFs) in the environment have rarely been reported due to the lack of sensitive analytical methods. Herein, a novel liquid chromatography-microwave plasma torch ionization-mass spectrometry (LC-MPTI-MS) technique was designed for the direct analysis of PFASFs in the environment. The collaborative action of reactive oxygen species (such as hydroxyl radicals) and the elevated temperature within the ambient MPTI environment results in the replacement of the fluorine atom in sulfonyl fluoride by oxygen, leading to the detection of perfluoroalkanesulfonic acid (PFSA) ions by MS. Concurrently, LC was employed to separate other PFSAs that are present in the environment. Three PFASFs exhibited good linearity within the range of 1-500 µg/L with R2 > 0.994. The limit of detections (LODs) and the limit of quantifications (LOQs) were measured at 39.32-87.87 and 131.07-292.90 ng/L, respectively. The method was utilized for the direct detection of spiked perfluorooctane sulfonyl fluoride (PFOSF) in wastewater with recoveries of 77.16 to 124.81%. Our approach circumvents the laborious process of chemical derivatization and is anticipated to serve as a robust tool for determining the levels and behaviors of PFASFs in the environment.

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Anal Chem / Anal. chem / Analytical chemistry Year: 2024 Document type: Article Affiliation country: China Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Anal Chem / Anal. chem / Analytical chemistry Year: 2024 Document type: Article Affiliation country: China Country of publication: United States