# Electrochemical Degradation of Perfluoroalkyl Sulfonates via Sulfonate to Carboxylate Conversion

**Authors:** Stella A. Fors, Richard J. Monsky, Emily R. Mahoney, Christian A. Malapit, William R. Dichtel

PMC · DOI: 10.1002/anie.202525896 · Angewandte Chemie (International Ed. in English) · 2026-01-09

## TL;DR

A new electrochemical method converts harmful perfluoroalkyl sulfonates into less toxic carboxylates, offering a promising way to degrade environmental pollutants.

## Contribution

A novel, scalable electrochemical method for degrading PFAS under non-aqueous conditions using commercial Pt electrodes.

## Key findings

- PFOS was efficiently converted to PFOA and shorter-chain carboxylates using Pt electrodes in acetonitrile.
- Degradation products were further mineralized to fluoride and non-fluorinated byproducts using DMSO/NaOH conditions.
- Significant fluorine and carbon loss was observed, likely due to volatile byproduct formation.

## Abstract

Efficient, scalable, and well‐understood methods for degrading per‐ and polyfluoroalkyl substances (PFAS) are essential for limiting their numerous negative human health and environmental effects. Electrochemical methods are promising for PFAS degradation but are currently not yet well developed for use in non‐aqueous conditions relevant for PFAS sorbent regeneration without resorting to specialized electrode materials. Herein, we report the mediated electrochemical conversion of perfluoroalkyl sulfonates to carboxylates using commercial Pt electrodes in acetonitrile. Perfluorooctane sulfonate (PFOS) was converted primarily to perfluorooctanoic acid (PFOA) alongside several shorter‐chain carboxylates through a proposed radical desulfonation and hydroxide coupling process explored in a detailed mechanistic study. Following the near‐complete conversion of PFOS to perfluoroalkyl carboxylates, all species are mineralized to fluoride and non‐fluorinated carbon byproducts using established low‐temperature DMSO/NaOH conditions. HPLC‐MS, ion chromatography, and quantitative nuclear magnetic resonance (NMR) methods determined a significant loss in fluorine and carbon balance after electrochemistry, which we attribute to the production of volatile byproducts. This degradation approach provides new insights into PFAS degradation mechanisms under highly oxidative, non‐aqueous conditions and highlights the potential for organic electrochemistry to address environmental challenges by promoting controlled and selective destruction pathways for common organic pollutants.

We demonstrate a novel approach for the degradation of perfluoroalkyl sulfonic acids (PFSAs) involving a controlled, electromediated, sulfonate‐to‐carboxylate headgroup conversion. We apply this method to shorter chain PFSAs and provide key mechanistic insights that contribute to a broader understanding of the molecular pathways underlying pollutant degradation and highlight the power of organic electrochemistry in addressing environmental challenges.

## Linked entities

- **Chemicals:** PFOS (PubChem CID 74483), PFOA (PubChem CID 9554), DMSO (PubChem CID 679), NaOH (PubChem CID 14798), acetonitrile (PubChem CID 6342)

## Full-text entities

- **Chemicals:** PFOS (MESH:C076994), PFOA (MESH:C023036), NaOH (MESH:D012972), fluorine (MESH:D005461), acetonitrile (MESH:C032159), fluoride (MESH:D005459), Carboxylate (-), per- and polyfluoroalkyl substances (MESH:D005466), DMSO (MESH:D004121), carbon (MESH:D002244), hydroxide (MESH:C031356), Pt (MESH:D010984), Sulfonate (MESH:D000476)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12887609/full.md

## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC12887609/full.md

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Source: https://tomesphere.com/paper/PMC12887609