Alkylidene functionalization produces highly recyclable and scalable polyhydroxyalkanoates

View at publisher
Authors: Li Zhou, James H. May, Ravikumar R. Gowda, Levi J. Hamernik, Jacob K. Kenny, Lili Wang, Christopher D Stubbs, Ethan C. Quinn, Jason S. DesVeaux, Katrina M. Knauer, Gregg T. Beckham, Eugene Y.-X. Chen
Cited by: 3
References: 69

Abstract

Recyclable polymers that can be produced at scale and readily tuned within the same polymer framework for specific properties are critical to achieving a circular materials economy. To this end, synthetic poly(3-hydroxyalkanoate)s (PHAs) have emerged as high-performance, chemically recyclable variants of biological PHAs, but their difficult monomer syntheses and suboptimal recycling efficiencies pose challenges for large-scale deployment. In this study, we investigated a β-isopropylidene PHA, i -PHA, for which the lactone monomer can be synthesized by existing industrial methods from biomass-derived isobutyric acid. The alkylidene substituent prevents decarboxylative degradation typically observed during PHA depolymerization, enabling near-quantitative chemical recycling to monomer. Controlled hydrogenation of the β-isopropylidene side group produces PHAs with diverse performance metrics that are competitive with a range of commodity polymers, spanning strong fibers to ductile thermoplastics to superglue epoxy resins.

Fields of Study & Subjects

biodegradable polymer synthesis and properties Carbon dioxide utilization in catalysis Catalysis for Biomass Conversion

Publication details

Journal / source
Science
Publisher
American Association for the Advancement of Science (AAAS)
Volume
392
Issue
6798
Pages
636–642
Publication date
7 May 2026
Language
EN