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Chemical recycling of polyesters and polycarbonates: why is zinc(II) such an effective depolymerization catalyst?

Abstract:

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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Publisher copy:
10.1021/jacs.5c16346

Authors

More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Role:
Author
More by this author
Institution:
University of Oxford
Division:
MPLS
Department:
Chemistry
Sub department:
Chemistry Research Laboratory
Oxford college:
St Catherine's College
Role:
Author
ORCID:
0000-0002-0734-1575


More from this funder
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:
1520-5126
ISSN:
0002-7863


Language:
English
Keywords:
Pubs id:
2320870
Local pid:
pubs:2320870
Deposit date:
2025-11-10
ARK identifier:

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