A fast and simple PFAS extraction method utilizing HR-CS-GFMAS for soil samples.
Fabian Simon1, Lennart Gehrenkemper1, Marcus von der Au1
1Federal Institute for Materials Research and Testing, Division 1.1 - Inorganic Trace Analysis, Richard-Willstätter-Straße 11, 12489, Berlin, Germany.
A new, faster method for extracting per- and polyfluorinated alkyl substances (PFASs) from soil has been developed. This optimized technique avoids solid phase extraction (SPE), providing more accurate results for extractable organically bound fluorine (EOF) analysis.
Area of Science:
- Environmental Chemistry
- Analytical Chemistry
Background:
- Per- and polyfluorinated alkyl substances (PFASs) are persistent environmental contaminants.
- Accurate quantification of PFASs in soil is crucial for environmental monitoring and risk assessment.
- Traditional methods often involve solid phase extraction (SPE), which can introduce bias.
Purpose of the Study:
- To develop an optimized, fast, and simple extraction method for PFAS determination in soils.
- To eliminate the bias associated with SPE in extractable organically bound fluorine (EOF) analysis.
- To provide a more accurate, economic, and ecological method for PFAS analysis.
Main Methods:
- Development of a liquid-solid extraction using acidified methanol.
- Implementation of a SPE-free approach for soil sample preparation.
- Utilized high resolution-continuum source-graphite furnace molecular absorption spectrometry (HR-CS-GFMAS) for EOF determination.
Main Results:
- The optimized SPE-free method achieved >80% extraction of EOF in four steps.
- Comparison revealed SPE significantly underestimated EOF concentrations by up to 94%.
- The method's procedural limit of quantification (LOQ) was 10.30 μg/kg, suitable for environmental samples.
Conclusions:
- The developed SPE-free extraction method is accurate, efficient, and cost-effective.
- Bypassing SPE provides a more reliable measurement of EOF in soils.
- This method is valuable for future PFAS monitoring and regulatory decisions.
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