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

IF 11.1 1区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ACS Central Science Pub Date : 2026-07-22 Epub Date: 2026-06-17 DOI:10.1021/acscentsci.6c00395
Jinsol Yook, Eric D. Rachita, Naba K. Kalita, Christopher J. Ellison* and Marc A. Hillmyer*, 
{"title":"Dramatic Enhancement in Polylactide Hydrolysis and Biodegradability Utilizing Low Levels of Organic Anhydrides As Masked Acids","authors":"Jinsol Yook,&nbsp;Eric D. Rachita,&nbsp;Naba K. Kalita,&nbsp;Christopher J. Ellison* and Marc A. Hillmyer*,&nbsp;","doi":"10.1021/acscentsci.6c00395","DOIUrl":null,"url":null,"abstract":"<p>Polylactide (PLA)\r\nis the world’s top synthetic biopolymer\r\nand a major contributor to the circular plastic economy by virtue\r\nof its biodegradation and full biomineralization into benign end products.\r\nNevertheless, efficient and complete degradation of PLA at its end\r\nof use remains constrained by the need for engineered industrial composting\r\nenvironments that operate at elevated temperatures and high humidity\r\nlevels. In this work, PLA samples containing low levels of phthalic\r\nor 2-sulfobenzoic acid anhydride additives were prepared using industrially\r\nviable melt-processing. These blends retained mechanical properties\r\nnearly identical to that of neat PLA while exhibiting significantly\r\naccelerated hydrolytic degradation, achieving appreciable mass losses\r\nwithin one month at 50 °C in artificial seawater. Remarkably,\r\neven trace (0.01 wt %, 100 ppm) incorporation of 2-sulfobenzoic acid\r\ncyclic anhydride proved highly effective in promoting PLA hydrolysis\r\neven at temperatures below the glass transition temperature of the\r\nparent material. Furthermore, incorporation of 2-sulfobenzoic acid\r\ncyclic anhydride (0.1 wt %) enabled rapid biodegradation under composting\r\nconditions at 58 °C, achieving 90% within 11 days, surpassing\r\nthat of neat PLA. Using anhydrides as strong acid-generating additives\r\nenables acceleration of PLA hydrolysis and biodegradation without\r\ncompromising its other attractive properties, thereby opening a viable\r\npathway toward realizing the full potential of PLA in a larger array\r\nof applications.</p>","PeriodicalId":10,"journal":{"name":"ACS Central Science","volume":"12 7","pages":"965–971"},"PeriodicalIF":11.1000,"publicationDate":"2026-07-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Central Science","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acscentsci.6c00395","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/6/17 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

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.

Abstract Image

利用低水平的有机酸酐作为掩蔽酸,显著提高聚丙交酯的水解和生物降解性。
聚乳酸(PLA)是世界顶级的合成生物聚合物,由于其生物降解和完全生物矿化成良性最终产品,是循环塑料经济的主要贡献者。然而,PLA在其使用结束时的有效和完全降解仍然受到工程工业堆肥环境的需求的限制,这些环境在高温和高湿水平下运行。在这项工作中,使用工业上可行的熔融加工制备了含有低水平邻苯二甲酸或2-巯基苯甲酸酸酐添加剂的PLA样品。这些共混物保持了与纯PLA几乎相同的机械性能,同时表现出明显加速的水解降解,在人工海水中50°C下一个月内实现了明显的质量损失。值得注意的是,即使在低于母体材料玻璃化转变温度的温度下,微量(0.01 wt %, 100 ppm)的2-磺酸环酸酐掺入也能有效地促进PLA水解。此外,加入2-磺酸苯甲酸环酸酐(0.1 wt %)可以在58°C的堆肥条件下快速生物降解,在11天内达到90%,超过纯PLA。使用酸酐作为强酸生成添加剂,可以加速PLA的水解和生物降解,而不会影响其其他有吸引力的特性,从而为实现PLA在更广泛应用中的全部潜力开辟了一条可行的途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
ACS Central Science
ACS Central Science Chemical Engineering-General Chemical Engineering
CiteScore
25.50
自引率
0.50%
发文量
194
审稿时长
10 weeks
期刊介绍: ACS Central Science publishes significant primary reports on research in chemistry and allied fields where chemical approaches are pivotal. As the first fully open-access journal by the American Chemical Society, it covers compelling and important contributions to the broad chemistry and scientific community. "Central science," a term popularized nearly 40 years ago, emphasizes chemistry's central role in connecting physical and life sciences, and fundamental sciences with applied disciplines like medicine and engineering. The journal focuses on exceptional quality articles, addressing advances in fundamental chemistry and interdisciplinary research.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书