# Single-pot mechanochemically-enabled fluorine atom closed-loop economy using PFASs as fluorinating agents

**Authors:** Hao Long, Georgina Kirby, Lutz Ackermann

PMC · DOI: 10.1038/s41467-026-70766-9 · 2026-03-20

## TL;DR

The paper introduces a simple, single-step method to break down harmful 'forever chemicals' and reuse their fluorine atoms in other molecules.

## Contribution

A novel mechanochemical defluorination method that enables fluorine recycling from PFASs without high temperatures or harsh reagents.

## Key findings

- The method efficiently transfers fluorine from PFASs to organic molecules in a single pot.
- It works on fluorinated polymers like PVDF and PTFE, enabling sustainable breakdown of persistent chemicals.
- The process requires minimal purification and scales well to larger quantities.

## Abstract

Per- and polyfluoroalkyl substances (PFASs), also known as “forever chemicals”, pose an increasing threat to the environment and human health. Despite recent advancements in PFASs destruction, the recycling processes for such molecules remain limited to methods using high-temperatures or strong reducing agents. Sustainable degradation methods for PFASs, along with the subsequent utilization or recycling of the resulting fluorides, are indeed highly beneficial. In this study, we present a user-friendly, single-pot mechanochemical defluorination approach for fluorine transfer from PFASs to organic molecules. The high efficiency of this mechanochemical system obviates subsequent purification steps, requiring only minimal solvent filtration, even on a decagram scale. Furthermore, this strategy can be extended to the defluorination of everyday fluoroplastic and fluorinated polymers, such as PVDF membranes, pipes, and PTFE, thus addressing a critical challenge in sustainably breaking down persistent and environmentally harmful “forever chemicals”.

In this study, the authors present a user-friendly, single-pot mechanochemical defluorination approach for fluorine transfer from per- and polyfluoroalkyl substances to organic molecules.

## Full-text entities

- **Genes:** PFAS (phosphoribosylformylglycinamidine synthase) [NCBI Gene 5198] {aka FGAMS, FGAR-AT, FGARAT, GATD8, PURL}, MLYCD (malonyl-CoA decarboxylase) [NCBI Gene 23417] {aka MCD}
- **Chemicals:** perfluorooctane (MESH:C073608), carbonate (MESH:D002254), phenylsulfonyl chlorides (MESH:C010544), F- (MESH:D005461), K2HPO4 (MESH:C013216), stainless-steel (MESH:D013193), vitamin E (MESH:D014810), oxalate (MESH:D010070), Melatonin (MESH:D008550), FEP (MESH:C096305), formate (MESH:C030544), H2O (MESH:D014867), olefin (MESH:D000475), delta-tocopherol (MESH:C479072), steroid (MESH:D013256), KOH (MESH:C029943), -steel (MESH:D013232), CHCl3 (MESH:D002725), 13C (MESH:C000615229), sulfonyl chloride (MESH:C044255), Diosgenin (MESH:D004144), TsF (MESH:C003614), C (MESH:D002244), TsCl (-), PTFE (MESH:D011138), polymer (MESH:D011108), PVDF (MESH:C024865), pyridine (MESH:C023666), Tosyl chloride (MESH:C025506), D2O (MESH:D017666), Ca(OH)2 (MESH:D002126), Quinidine (MESH:D011802), ZrO2 (MESH:C028541), ethylene tetrafluoroethylene (MESH:C040378), Sulfonyl fluorides (MESH:C048899), fluoride (MESH:D005459), Per- and polyfluoroalkyl substances (MESH:D005466), alcohols (MESH:D000438), diacetone-d-glucose (MESH:C036124), celite (MESH:D007692)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC13009461/full.md

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Source: https://tomesphere.com/paper/PMC13009461