Designed to Degrade: Tailoring Polyesters for Circularity

• Published in: Chemical reviews Vol. 124; no. 13; pp. 8473 - 8515
• Main Authors: Aarsen, Celine V., Liguori, Anna, Mattsson, Rebecca, Sipponen, Mika H., Hakkarainen, Minna
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 10-07-2024
• Subjects: Biodegradation; Bioplastics; Catalysts; Chemical bonds; Chemical recycling; Circularity; Design; Design for recycling; End of life; Environmental conditions; Functional groups; Molecular chains; Plastics; Polyester resins; Polyesters; Polyethylene terephthalate; Recycled materials
• ISSN: 0009-2665; 1520-6890; 1520-6890
• DOI: 10.1021/acs.chemrev.4c00032

A powerful toolbox is needed to turn the linear plastic economy into circular. Development of materials designed for mechanical recycling, chemical recycling, and/or biodegradation in targeted end-of-life environment are all necessary puzzle pieces in this process. Polyesters, with reversible ester bonds, are already forerunners in plastic circularity: poly­(ethylene terephthalate) (PET) is the most recycled plastic material suitable for mechanical and chemical recycling, while common aliphatic polyesters are biodegradable under favorable conditions, such as industrial compost. However, this circular design needs to be further tailored for different end-of-life options to enable chemical recycling under greener conditions and/or rapid enough biodegradation even under less favorable environmental conditions. Here, we discuss molecular design of the polyester chain targeting enhancement of circularity by incorporation of more easily hydrolyzable ester bonds, additional dynamic bonds, or degradation catalyzing functional groups as part of the polyester chain. The utilization of polyester circularity to design replacement materials for current volume plastics is also reviewed as well as embedment of green catalysts, such as enzymes in biodegradable polyester matrices to facilitate the degradation process.