From Polymers to Rings and Back Again: Chemical Recycling of Polyesters to Macrolactones

Cyclic anhydride and epoxide ring-opening copolymerization is a versatile and controlled route to make polyesters, gaining attention in different application sectors. But so far, the chemical recycling of these polyesters to cyclic monomers is under-explored. Here, the catalytic chemical recycling of aliphatic polyesters to selectively form 16- and 18-membered lactones is presented. The recycling reactions are catalyzed using commercial tin(II) octoate and conducted in the polymer melt (230 °C) resulting in high conversions to the macrolactones (>90%). The recycled macrolactones undergo catalyzed ring-opening polymerizations to produce polyesters with equivalent properties to the virgin materials.

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Publication Details

Journal
Angewandte Chemie International Edition
Published
2025-03-11
DOI
https://doi.org/10.1002/anie.202423478
Citations
9
Primary Topic
biodegradable polymer synthesis and properties
Type
article
Field-Weighted Citation Impact
5.37
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article

From Polymers to Rings and Back Again: Chemical Recycling of Polyesters to Macrolactones

Charlotte K. Williams, Ryan W. F. Kerr, Thomas M. McGuire, Madeleine L. Smith
9 citations
Angewandte Chemie International Edition
biodegradable polymer synthesis and properties
5.37
article

From Polymers to Rings and Back Again: Chemical Recycling of Polyesters to Macrolactones

Charlotte K. Williams, Ryan W. F. Kerr, Thomas M. McGuire, Madeleine L. Smith
article en
9 citations

Abstract

Cyclic anhydride and epoxide ring-opening copolymerization is a versatile and controlled route to make polyesters, gaining attention in different application sectors. But so far, the chemical recycling of these polyesters to cyclic monomers is under-explored. Here, the catalytic chemical recycling of aliphatic polyesters to selectively form 16- and 18-membered lactones is presented. The recycling reactions are catalyzed using commercial tin(II) octoate and conducted in the polymer melt (230 °C) resulting in high conversions to the macrolactones (>90%). The recycled macrolactones undergo catalyzed ring-opening polymerizations to produce polyesters with equivalent properties to the virgin materials.

Angewandte Chemie International EditionVol. 64(21)
Mansfield University (US), Oxford Research Group (GB), University of Oxford (GB)
Openalex Percentile: Top 4%
biodegradable polymer synthesis and properties
5.37
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