Dramatic Enhancement in Polylactide Hydrolysis and Biodegradability Utilizing Low Levels of Organic Anhydrides As Masked Acids

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Authors: Jinsol Yook, Eric D. Rachita, Naba Kumar Kalita, Christopher J. Ellison, Marc A. Hillmyer
Cited by: 1
References: 35

Abstract

Polylactide (PLA) is the world's top synthetic biopolymer and a major contributor to the circular plastic economy by virtue of its biodegradation and full biomineralization into benign end products. Nevertheless, efficient and complete degradation of PLA at its end of use remains constrained by the need for engineered industrial composting environments that operate at elevated temperatures and high humidity levels. In this work, PLA samples containing low levels of phthalic or 2-sulfobenzoic acid anhydride additives were prepared using industrially viable melt-processing. These blends retained mechanical properties nearly identical to that of neat PLA while exhibiting significantly accelerated hydrolytic degradation, achieving appreciable mass losses within one month at 50 °C in artificial seawater. Remarkably, even trace (0.01 wt %, 100 ppm) incorporation of 2-sulfobenzoic acid cyclic anhydride proved highly effective in promoting PLA hydrolysis even at temperatures below the glass transition temperature of the parent material. Furthermore, incorporation of 2-sulfobenzoic acid cyclic anhydride (0.1 wt %) enabled rapid biodegradation under composting conditions at 58 °C, achieving 90% within 11 days, surpassing that of neat PLA. Using anhydrides as strong acid-generating additives enables acceleration of PLA hydrolysis and biodegradation without compromising its other attractive properties, thereby opening a viable pathway toward realizing the full potential of PLA in a larger array of applications.

Fields of Study & Subjects

biodegradable polymer synthesis and properties Microplastics and Plastic Pollution Polymer crystallization and properties

Publication details

Journal / source
ACS Central Science
Publisher
American Chemical Society (ACS)
Volume
12
Issue
7
Pages
965–971
Publication date
17 June 2026
Language
EN