Anna Kruglhuber, Clemens Bernhard, Susanne Boye, Markus Wierer, Albena Lederer, Clemens Schwarzinger, Klara M. Saller
{"title":"Synthesis of Functional Water-Soluble Polyesters Based on Citric Acid and Dimethylolpropionic Acid","authors":"Anna Kruglhuber, Clemens Bernhard, Susanne Boye, Markus Wierer, Albena Lederer, Clemens Schwarzinger, Klara M. Saller","doi":"10.1021/acspolymersau.5c00196","DOIUrl":null,"url":null,"abstract":"<p>Aiming for renewable polymers with potential recyclability\r\nand\r\nbiodegradability, polyesters are very promising due to an increasing\r\nnumber of available biobased monomers and ester bonds that can be\r\nhydrolyzed under specific conditions. Citric acid, for example, is\r\na biobased, nontoxic, cheap, and easily available resource. Its multifunctionality\r\nenables the synthesis of polyesters with free carboxy groups, thus\r\nproviding possibilities for further functionalization and cross-linking.\r\nCitric acid and dimethylolpropionic acid were used to synthesize water-soluble\r\npolyesters via melt polycondensation at 150 °C without the need\r\nfor potentially hazardous catalysts. The resulting polyesters displayed\r\na significant amount of free carboxylic acid groups (8 mmol g<sub>polyester</sub><sup>–1</sup>), and reasonable number-average\r\nmolar masses up to 5200 g mol<sup>–1</sup>. Via postsynthetical\r\n(partial) neutralization procedures using KOH, charged moieties could\r\nbe successfully incorporated to further increase hydrophilicity. The\r\ndegree of neutralization proved to be well controllable. This enables\r\ntunability of the final properties, as remaining free carboxy groups\r\ncan be used for further modifications. Alternative to carboxylate\r\nmoieties, the introduction of sulfonate groups promotes hydrophilicity.\r\nFor this purpose, unsaturated polyesters were synthesized that contained\r\nvarying amounts of maleic anhydride as a third monomer. Postsynthetical\r\nsulfonation was performed via the Michael addition of sodium sulfite,\r\nintroducing a significant number of sulfonate groups. Neutralization\r\nand sulfonation were performed in aqueous solution, leading to slight\r\ndecreases in molar mass due to hydrolysis. The extent of the reduction\r\nwas successfully reduced by optimizing both procedures. The synthesized\r\nwater-soluble polyesters carry a substantial number of functional\r\ngroups. They have high potential as precondensates for cross-linked,\r\nwater-absorbing materials to be used in agriculture and biomedicine,\r\nfor which biodegradability is a crucial property.</p>","PeriodicalId":72049,"journal":{"name":"ACS polymers Au","volume":"6 2","pages":"610–621"},"PeriodicalIF":6.7000,"publicationDate":"2026-04-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS polymers Au","FirstCategoryId":"1085","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acspolymersau.5c00196","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2026/2/20 0:00:00","PubModel":"Epub","JCR":"Q1","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
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.