Analytica chimica acta · 2025
Effective preconcentration of volatile per- and polyfluoroalkyl substances from gas and aqueous phase via solid phase microextraction.
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Martínez-Pérez-Cejuela Héctor, Williams Madison L, McLeod Chloe, Gionfriddo Emanuela
Аннотация
BACKGROUND: Per- and polyfluoroalkyl substances (PFAS) are synthetic fluorinated chemicals of increasing global concern due to their persistence, toxicity, and widespread presence in the environment. Neutral and volatile PFAS, used in firefighting foams and non-stick coatings, are precursors of perfluorinated acids such as perfluorooctanesulfonic acid (PFOS) and perfluorooctanoic acid (PFOA) and necessitate effective preconcentration methods for isolation from aqueous and gaseous phases.
RESULTS: In this work, a robust quantitative method was rigorously optimized and validated to achieve effective preconcentration and quantification of neutral volatile PFAS, including fluorotelomer alcohols (FTOHs), perfluorooctanesulfonamides (FOSAs), and a perfluorooctanesulfonamido-ethanol (FOSE). Leveraging the versatility of solid phase microextraction (SPME) for sampling in different extraction modes, volatile PFAS were pre-concentrated in gaseous (Headspace-SPME) and aqueous (Direct Immersion-SPME) phases. The impact of temperature, time, and aqueous media composition on extraction efficiency was assessed, with analysis performed using gas chromatography-mass spectrometry. LOQs between 0.005 μg L-1 and 5 μg L-1 were achieved for direct immersion-SPME and 0.005 μg L-1 to 0.25 μg L-1 for headspace-SPME, also demonstrating excellent repeatability with relative standard deviations (RSD%) below 11 %.
SIGNIFICANCE: This work highlights the need for efficient pre-chromatographic separation methods for extraction and preconcentration of volatile PFAS. The developed Headspace and Direct Immersion-SPME methods provide a practical, solvent-free, automated solution for extraction and preconcentration of volatile PFAS from aqueous and gaseous samples. These methods enrich the analytical toolbox for PFAS analysis and can be applied to understanding how PFAS enter the environment and partition in heterogeneous systems.
RESULTS: In this work, a robust quantitative method was rigorously optimized and validated to achieve effective preconcentration and quantification of neutral volatile PFAS, including fluorotelomer alcohols (FTOHs), perfluorooctanesulfonamides (FOSAs), and a perfluorooctanesulfonamido-ethanol (FOSE). Leveraging the versatility of solid phase microextraction (SPME) for sampling in different extraction modes, volatile PFAS were pre-concentrated in gaseous (Headspace-SPME) and aqueous (Direct Immersion-SPME) phases. The impact of temperature, time, and aqueous media composition on extraction efficiency was assessed, with analysis performed using gas chromatography-mass spectrometry. LOQs between 0.005 μg L-1 and 5 μg L-1 were achieved for direct immersion-SPME and 0.005 μg L-1 to 0.25 μg L-1 for headspace-SPME, also demonstrating excellent repeatability with relative standard deviations (RSD%) below 11 %.
SIGNIFICANCE: This work highlights the need for efficient pre-chromatographic separation methods for extraction and preconcentration of volatile PFAS. The developed Headspace and Direct Immersion-SPME methods provide a practical, solvent-free, automated solution for extraction and preconcentration of volatile PFAS from aqueous and gaseous samples. These methods enrich the analytical toolbox for PFAS analysis and can be applied to understanding how PFAS enter the environment and partition in heterogeneous systems.