# Photo-initiated solvent-mediated depolymerization of consumer poly(methyl methacrylate) without chlorinated reagents

**Authors:** Jonathan T. Husband, Gavin Irvine, Callum R. Morris, Andrea Folli, Matthew G. Davidson, Simon J. Freakley

PMC · DOI: 10.1038/s41467-025-67997-7 · Nature Communications · 2026-01-28

## TL;DR

Scientists developed a low-temperature method to recycle PMMA plastic into its original monomer using UV light and non-chlorinated solvents.

## Contribution

A new low-temperature chemical recycling method for PMMA that does not require chlorinated reagents.

## Key findings

- PMMA can be efficiently depolymerized at 120-180°C using UV light in oxygen-free conditions.
- Non-chlorinated solvents like benzonitrile enable complete unzipping of PMMA without radical termination.
- Chlorine radicals are not essential for depolymerization but can functionalize PMMA for upcycling.

## Abstract

The chemical recycling of commodity acrylic polymers, such as the transparent thermoplastic polymethyl methacrylate (PMMA), typically requires temperatures of 350-400°C. Herein, we report chemical recycling back to monomers for PMMA between 120-180°C, through UV illumination under oxygen-free conditions. We have achieved gram-scale degradation of consumer plastic with >95% conversion, yielding >70% monomer, which can be readily repolymerized. The process proceeds even at high concentrations (>1 M) and depends strongly on solvent choice: aromatic solvents like dichlorobenzene and diphenyl ether maximize conversion. In contrast to a concurrently published study, we report that chlorine radicals are not required for depolymerization; however, when present, they react with the unzipping chain to form chlorine-functionalized PMMA which can be upcycled through derivatization. In more sustainable non-chlorinated solvents such as benzonitrile, minimal termination by radicals enables complete unzipping. These findings demonstrate a low-temperature, scalable route for the chemical recycling of PMMA, offering alternative pathways for plastic circularity.

Chemical recycling of poly(methyl methacrylate) (PMMA) typically requires high temperatures. Here, the authors report the UV-initiated depolymerisation of PMMA at low temperatures, in non-chlorinated solvents, such as benzonitrile.

## Linked entities

- **Chemicals:** diphenyl ether (PubChem CID 7583), benzonitrile (PubChem CID 7505)

## Full-text entities

- **Diseases:** depression (MESH:D003866), Tc (MESH:D000377)
- **Chemicals:** copper (MESH:D003300), alkane (MESH:D000473), polymethacrylates (MESH:C030613), N-methyl-2-pyrrolidone (MESH:C038678), oxygen (MESH:D010100), Polystyrene (MESH:D011137), alkene (MESH:D000475), 2-chloroethanol (MESH:D005023), DMSO (MESH:D004121), Polymer (MESH:D011108), tosyl chloride (MESH:C025506), argon (MESH:D001128), dichloromethane (MESH:D008752), AIBN (MESH:C004526), carbon (MESH:D002244), 4-Cyano-4-[(dodecylsulfanylthiocarbonyl)sulfanyl]pentanoic acid (MESH:C000709520), polyesters (MESH:D011091), H2O (MESH:D014867), Br (MESH:D001966), PMMA (MESH:D019904), phthalimide (MESH:C037431), dioxane (MESH:C025223), oil (MESH:D009821), hydrogen (MESH:D006859), aluminum (MESH:D000535), Mn (MESH:D008345), acridine orange (MESH:D000165), alpha-methylstyrene (MESH:C017915), benzene (MESH:D001554), 5,5-dimethyl-1-pyrroline-N-oxide (MESH:C017245), sulfolane (MESH:C013693), amide (MESH:D000577), N-tert-butyl-alpha-phenylnitrone (MESH:C029217), KOH (MESH:C029943), methanol (MESH:D000432), C-Cl (MESH:D002433), N2 (MESH:D009584), diethyl ether (MESH:D004986), chlorobenzene (MESH:C031294), diphenyl ether (MESH:C031538), MMA (MESH:D020366), THF (MESH:C018674), benzonitrile (MESH:C014356), xylenes (MESH:D014992), copper (II) chloride (MESH:C029892), anisole (MESH:C060998), iron (MESH:D007501), PLA (MESH:C033616), alumina (MESH:D000537), tris(2-pyridylmethyl)amine (MESH:C431843), methacrylates (MESH:D008689), DMF (-), Cl (MESH:D002713)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12864808/full.md

## References

5 references — full list in the complete paper: https://tomesphere.com/paper/PMC12864808/full.md

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Source: https://tomesphere.com/paper/PMC12864808