A novel methodology for the determination of neutral perfluoroalkyl and polyfluoroalkyl substances in water by gas chromatographyatmospheric pressure photoionisation-high resolution mass spectrometry

Publication date

2026-01-21T17:55:21Z

2026-01-21T17:55:21Z

2020-03-01

2026-01-21T17:55:21Z

Abstract

Here, we developed and validated a new gas chromatography-atmospheric pressure photoionisation high-resolution mass spectrometry (GC-APPI-HRMS) method combined with headspace solid-phase microextraction (HS-SPME) for the determination of neutral perfluoroalkyl and polyfluoroalkyl substances (PFASs) in water samples. The method includes fluorotelomer olefins (FTOs), fluorotelomer alcohols (FTOHs), fluoroctanesulfonamides (FOSAs) and sulfonamido-ethanols (FOSEs). The feasibility of the GC-APPI interface for the ionisation of the target compounds was evaluated, achieving the best results using negative-ion dopant-assisted ionisation with acetone and a source and capillary temperatures of 225 oC and 175 oC, respectively. Under optimal conditions, FTOs and FTOHs mass spectra showed intense in-source CID fragment ions from the fluoroalkyl chain but also the superoxide [M+O2]-· adduct ion. For FOSAs, [M-H]- was the main ion generated, while FOSEs mass spectra showed fragment ions corresponding to the different cleavages of the functional group. The high ionisation efficiency achieved with the GC-APPI interface provided limits of the detection lower than those obtained using traditional GC-MS ionisation techniques, with a high sensitivity, selectivity and precision. For water analysis, a fast and simple HS-SPME procedure was developed, avoiding evaporation steps, which could lead to the loss of the most volatile compounds. The developed HS-SPME GC-APPI-HRMS method showed a good analytical performance for the analysis of river water samples, providing very low limits of detection (0.02e15 ng L 1), good repeatability (RSD < 11%) and trueness (relative error < 12%).

Document Type

Article


Accepted version

Language

English

Publisher

Elsevier B.V.

Related items

Versió postprint del document publicat a: https://doi.org/10.1016/j.aca.2019.12.004

Analytica Chimica Acta, 2020, vol. 1100, p. 97-106

https://doi.org/10.1016/j.aca.2019.12.004

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Rights

cc-by-nc-nd (c) Elsevier B.V., 2020

http://creativecommons.org/licenses/by-nc-nd/4.0/

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