Journal article
Chemical recycling of polyesters and polycarbonates: why is zinc(II) such an effective depolymerization catalyst?
- Abstract:
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Effective polymer recycling is essential to reduce plastic pollution; catalytic polymer recycling to monomer is particularly attractive as it could operate over multiple closed-loop cycles. Aliphatic polyesters and carbonates show properties that compete with current plastics and can be depolymerized to 6- and 7-membered cyclic ester or carbonate monomers. Nonetheless, the rules governing the recycling catalyst selection are unclear. Here, Zn(II), Co(II), Mg(II), Sn(II), Ca(II), Ba(II), Y(III) and Bi(III) 2-ethyl hexanoate catalysts, are compared for the chemical recycling of 6 different oxygenated polymers, in bulk, at low catalysts loadings (1:100 – 1:1000) and temperatures (90-170 °C). All metals are selective for recycling to monomer but show clear differences in rates; the Zn(II) catalyst is always the most active. Using linear free energy analysis, the depolymerization rate constant directly correlates with the metal’s Lewis acidity, as assessed by its hydrolysis constant. The best catalysts comprise metals with intermediate acidity, i.e. Zn(II), Co(II) and Mg(II). The structure-activity correlation applies to polymers that have primary or secondary chain-end group alcohols, 6- or 7-atom repeat units and those featuring ester or carbonate linkages. Eyring analysis using Zn(II), Co(II), Mg(II) and Sn(II) catalysts shows that the Zn(II) catalysts balance competing transition-state enthalpy (ΔHǂd) and entropy (ΔSǂd) demands. Density functional theory calculations of key transition states suggest that Zn(II) is particularly effective because it both activates the polymer carbonyl group and labilises the alkoxide nucleophile. These generally applicable linear free energy relationships are important tools to minimize energy input and maximise performances in future recycling processes.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Supplementary materials, pdf, 3.1MB, Terms of use)
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(Preview, Version of record, pdf, 2.4MB, Terms of use)
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- Publisher copy:
- 10.1021/jacs.5c16346
Authors
- Funder identifier:
- https://ror.org/0439y7842
- Grant:
- EP/Z532782/1
- EP/R027129/1
- EP/S018603/1
- Publisher:
- American Chemical Society
- Journal:
- Journal of the American Chemical Society More from this journal
- Volume:
- 147
- Issue:
- 46
- Pages:
- 43077-43085
- Publication date:
- 2025-11-10
- Acceptance date:
- 2025-10-28
- DOI:
- EISSN:
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1520-5126
- ISSN:
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0002-7863
- Language:
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English
- Keywords:
- Pubs id:
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2320870
- Local pid:
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pubs:2320870
- Deposit date:
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2025-11-10
- ARK identifier:
Terms of use
- Copyright holder:
- McGuire et al.
- Copyright date:
- 2025
- Rights statement:
- Copyright © 2025 The Authors. Published by American Chemical Society. This publication is licensed under CC-BY 4.0.
- Licence:
- CC Attribution (CC BY)
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