Synthesis of Functional Water-Soluble Polyesters Based on Citric Acid and Dimethylolpropionic Acid.

IF 6.9 Q1 POLYMER SCIENCE
ACS polymers Au Pub Date : 2026-02-20 eCollection Date: 2026-04-08 DOI:10.1021/acspolymersau.5c00196
Anna Kruglhuber, Clemens Bernhard, Susanne Boye, Markus Wierer, Albena Lederer, Clemens Schwarzinger, Klara M Saller
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引用次数: 0

Abstract

Aiming for renewable polymers with potential recyclability and biodegradability, polyesters are very promising due to an increasing number of available biobased monomers and ester bonds that can be hydrolyzed under specific conditions. Citric acid, for example, is a biobased, nontoxic, cheap, and easily available resource. Its multifunctionality enables the synthesis of polyesters with free carboxy groups, thus providing possibilities for further functionalization and cross-linking. Citric acid and dimethylolpropionic acid were used to synthesize water-soluble polyesters via melt polycondensation at 150 °C without the need for potentially hazardous catalysts. The resulting polyesters displayed a significant amount of free carboxylic acid groups (8 mmol gpolyester -1), and reasonable number-average molar masses up to 5200 g mol-1. Via postsynthetical (partial) neutralization procedures using KOH, charged moieties could be successfully incorporated to further increase hydrophilicity. The degree of neutralization proved to be well controllable. This enables tunability of the final properties, as remaining free carboxy groups can be used for further modifications. Alternative to carboxylate moieties, the introduction of sulfonate groups promotes hydrophilicity. For this purpose, unsaturated polyesters were synthesized that contained varying amounts of maleic anhydride as a third monomer. Postsynthetical sulfonation was performed via the Michael addition of sodium sulfite, introducing a significant number of sulfonate groups. Neutralization and sulfonation were performed in aqueous solution, leading to slight decreases in molar mass due to hydrolysis. The extent of the reduction was successfully reduced by optimizing both procedures. The synthesized water-soluble polyesters carry a substantial number of functional groups. They have high potential as precondensates for cross-linked, water-absorbing materials to be used in agriculture and biomedicine, for which biodegradability is a crucial property.

基于柠檬酸和二甲基丙酸的功能性水溶性聚酯的合成。
针对具有潜在可回收性和生物降解性的可再生聚合物,聚酯是非常有前途的,因为越来越多的生物基单体和酯键可以在特定条件下水解。例如,柠檬酸是一种生物基、无毒、廉价且容易获得的资源。它的多功能性使其能够合成具有游离羧基的聚酯,从而为进一步的功能化和交联提供了可能性。用柠檬酸和二甲基丙酸在150℃下通过熔融缩聚合成水溶性聚酯,无需使用有潜在危险的催化剂。所得聚酯显示出大量的游离羧酸基团(8 mmol gpolyester -1),合理的数平均摩尔质量可达5200 g mol-1。通过使用KOH的合成后(部分)中和程序,带电部分可以成功地结合以进一步提高亲水性。中和度是可控的。这使得最终性质具有可调性,因为剩余的游离羧基可用于进一步修改。替代羧酸基团,引入磺酸基促进亲水性。为此,合成了含有不同数量的马来酸酐作为第三单体的不饱和聚酯。合成后磺化是通过亚硫酸钠的迈克尔加成进行的,引入了大量的磺酸基。在水溶液中进行中和和磺化,由于水解导致摩尔质量略有下降。通过优化这两个程序,成功地减小了减小的程度。合成的水溶性聚酯含有大量的官能团。它们作为交联吸水材料的预冷凝物具有很高的潜力,可用于农业和生物医学,生物可降解性是其关键特性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
2.50
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