Per- and polyfluoroalkyl substances (PFAS) are man-made organofluorine chemicals that can contaminate environmental waters and have gained worldwide attention over the past two decades. PFAS are most frequently detected by mass spectrometric targeted analysis methods which may not detect all the PFAS in samples. This report describes the investigation of adsorbable organofluorine (AOF) with detection by combustion ion chromatography (CIC) for detection of PFAS in surface waters and wastewaters that adsorb to granular activated carbon (GAC) with the recognition that this technique measures more than just PFAS. Overall mean recoveries of 77-120% were obtained in 17 of the 18 tested surface water and wastewater matrices spiked with perfluoropentane sulfonate (PFPeS) and 55-119% mean recoveries were obtained in 11 of the 12 surface water and wastewater matrices spiked with a PFAS mixture. Poor method performance (34-39% mean recoveries) was observed in landfill leachate wastewater. Method detection limits of 1.4-2.2 μg L were achieved using 100 mL sample volumes adsorbed onto commercially available GAC. This report demonstrates that this AOF technique can be a useful screening tool for estimating organofluorine concentrations when PFAS contamination is suspected.
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http://dx.doi.org/10.1039/d2ay01121b | DOI Listing |
J Hazard Mater
December 2024
Institute of Aquatic Ecology, HUN-REN Centre for Ecological Research Budapest, Hungary; National Laboratory for Water Science and Water Security, Institute of Aquatic Ecology, HUN-REN Centre for Ecological Research, Budapest, Hungary; Institute of Chemistry, Eötvös Loránd University, Budapest, Hungary. Electronic address:
The existing technologies in municipal wastewater treatment plants are ineffective in eliminating persistent fluorine-containing contaminants. At the same time, there is an increasing demand for novel organofluorine compounds, particularly in the production of lithium-ion batteries, as well as in the agrochemical and pharmaceutical sectors for more efficient ingredients. This implies that we must account for ongoing changes in the fluorine levels within riverine environments.
View Article and Find Full Text PDFJ Hazard Mater
December 2024
Center for Environmental Solutions & Emergency Response, US Environmental Protection Agency, Cincinnati, OH, USA; Department of Chemical and Biomolecular Engineering, Rice University, Houston, TX, USA. Electronic address:
J Hazard Mater
November 2024
Department of Environmental Sciences, University of California, Riverside, CA 92521, United States; Environmental Toxicology Graduate Program, University of California, Riverside, CA 92521, United States. Electronic address:
J Sep Sci
August 2024
Department of Chemistry and Biochemistry, The University of Texas at Arlington, Arlington, Texas, USA.
Poly- and perfluoroalkyl substances (PFAS) are a class of persistent organic pollutants whose high stability and appreciable water solubility have led to near-global contamination. PFAS are bioaccumulative toxins that have been linked to a myriad of disorders and have been detected nearly universally in human blood. Liquid chromatography-tandem mass spectrometry is the most frequent method used for quantitation, though this typically only measures a few dozen of the >14 000 known PFAS and has been shown to account for a small portion of the total organic fluorine present.
View Article and Find Full Text PDFRSC Adv
May 2024
Nanosystems Engineering Research Center for Nanotechnology-Enabled Water Treatment, School of Sustainable Engineering and the Built Environment, Arizona State University Tempe Arizona USA +480-965-2885.
Per- and polyfluoroalkyl substances (PFAS) are pervasive in industrial processes, eliciting public concern upon their release into municipal sewers or the environment. Removing PFAS from the environment has become an urgent need. However, because potential endpoints span from energy-intensive complete mineralization to partial PFAS transformation, understanding and developing metrics for evaluating PFAS treatment can be a challenge.
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