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Biodegradable [(A) x B] n Alternating Copolyester: Achieving PET-like Performance with Enhanced Marine Degradation

Macromolecules 2026 Score: 40 ? 0–100 AI score estimating relevance to the microplastics field. Papers below 30 are filtered from public browse.
Jielin Xu, Jielin Xu, Zhenguang Li, Zhenguang Li, Yaning Wang, Shiyan Chen, Huaping Wang, Huaping Wang, Jing Wu, Jing Wu

Summary

Scientists engineered a new biodegradable copolyester with mechanical properties matching PET plastic — including high strength and flexibility — while achieving 60% mass loss in 90 days in marine water environments. This breakthrough is significant because it offers a potential drop-in replacement for PET that degrades in seawater rather than fragmenting into persistent microplastics.

Polymers
Study Type Environmental

The development of high-performance biodegradable polymers that simultaneously achieve petrochemical-plastic-like mechanical properties and controlled environmental degradability remains an unsolved challenge in sustainable materials science. We present an [(A)xB]n alternating copolyester platform engineered through a precision cascade polycondensation-ring-opening polymerization (PROP) strategy, featuring (i) ultrashort succinic acid (SA) soft segments (B), (ii) architecturally tuned hard-segment ((A)x) lengths, and (iii) spherulite-size-modulated semicrystalline morphology. This triple-design strategy yields unprecedented property combinations: 61 MPa yield strength and 428% elongation at break, matching PET’s elastic-plastic behavior (<300% strain) while exhibiting superior marine degradability (60% mass loss in 90 days across lake/seawater). The material further enables closed-loop chemical recycling to high-purity glycolic acid, establishing a new paradigm for circular polymer design that addresses both microplastic generation and end-of-life management challenges.

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