Bromine-photosensitized degradation of perfluorooctanoic acid

Abstract Per- and polyfluoroalkyl substances (PFAS) have been decomposed photochemically by using manganese dioxide (MnO2) as oxidant, sulfuric acid (H2SO4) as solvent, and bromine (Br2) as photocatalyst, to produce several smaller organofluorine compounds, and ultimately a yield of up to 4% of the...

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Main Authors: Jack C. Pocorobba, Mark S. Braiman
Format: Article
Language:English
Published: Nature Portfolio 2025-07-01
Series:Scientific Reports
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Online Access:https://doi.org/10.1038/s41598-025-06632-3
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author Jack C. Pocorobba
Mark S. Braiman
author_facet Jack C. Pocorobba
Mark S. Braiman
author_sort Jack C. Pocorobba
collection DOAJ
description Abstract Per- and polyfluoroalkyl substances (PFAS) have been decomposed photochemically by using manganese dioxide (MnO2) as oxidant, sulfuric acid (H2SO4) as solvent, and bromine (Br2) as photocatalyst, to produce several smaller organofluorine compounds, and ultimately a yield of up to 4% of the fluorine as HF. These fluorinated intermediates and product have been characterized with 19F NMR spectroscopy. The carbon from the PFAS was converted to CO2 with a detected yield of up to 10–15%. The reagents and apparatus to carry out this degradation are inexpensive and readily obtained, especially because NaBr can be substituted for Br2 as the sole source of bromine. A similar set of end products were observed with either perfluorooctanoic acid or polytetrafluoroethylene, demonstrating this process can possibly be used to degrade a variety of PFAS. Our results demonstrate the ability to degrade PFAS in a simple, controlled manner at lower temperatures and using less expensive reagents than current industrial methods.
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spelling doaj-art-b56c344eebb24ff6a6e8a300e0de0f562025-08-20T03:03:33ZengNature PortfolioScientific Reports2045-23222025-07-0115111210.1038/s41598-025-06632-3Bromine-photosensitized degradation of perfluorooctanoic acidJack C. Pocorobba0Mark S. Braiman1Department of Chemistry, Syracuse UniversityDepartment of Chemistry, Syracuse UniversityAbstract Per- and polyfluoroalkyl substances (PFAS) have been decomposed photochemically by using manganese dioxide (MnO2) as oxidant, sulfuric acid (H2SO4) as solvent, and bromine (Br2) as photocatalyst, to produce several smaller organofluorine compounds, and ultimately a yield of up to 4% of the fluorine as HF. These fluorinated intermediates and product have been characterized with 19F NMR spectroscopy. The carbon from the PFAS was converted to CO2 with a detected yield of up to 10–15%. The reagents and apparatus to carry out this degradation are inexpensive and readily obtained, especially because NaBr can be substituted for Br2 as the sole source of bromine. A similar set of end products were observed with either perfluorooctanoic acid or polytetrafluoroethylene, demonstrating this process can possibly be used to degrade a variety of PFAS. Our results demonstrate the ability to degrade PFAS in a simple, controlled manner at lower temperatures and using less expensive reagents than current industrial methods.https://doi.org/10.1038/s41598-025-06632-3Forever chemicalsPFAS decompositionPhotocatalysisInorganic fluoride
spellingShingle Jack C. Pocorobba
Mark S. Braiman
Bromine-photosensitized degradation of perfluorooctanoic acid
Scientific Reports
Forever chemicals
PFAS decomposition
Photocatalysis
Inorganic fluoride
title Bromine-photosensitized degradation of perfluorooctanoic acid
title_full Bromine-photosensitized degradation of perfluorooctanoic acid
title_fullStr Bromine-photosensitized degradation of perfluorooctanoic acid
title_full_unstemmed Bromine-photosensitized degradation of perfluorooctanoic acid
title_short Bromine-photosensitized degradation of perfluorooctanoic acid
title_sort bromine photosensitized degradation of perfluorooctanoic acid
topic Forever chemicals
PFAS decomposition
Photocatalysis
Inorganic fluoride
url https://doi.org/10.1038/s41598-025-06632-3
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