{"title":"由海藻酸盐、阴离子纤维素和壳聚糖组成的ph敏感水凝胶中膨胀和收缩动力学的数学建模","authors":"Aleš Ručigaj, Tilen Kopač","doi":"10.1016/j.polymer.2025.128452","DOIUrl":null,"url":null,"abstract":"<div><div>This study develops a mathematical model to predict the swelling and shrinkage dynamics of pH-sensitive hydrogels composed of alginate, TEMPO-oxidized cellulose nanofibers (TOCNF), or chitosan. We investigated the effects of biopolymer type, cross-linking density, and/or pH conditions on hydrogel behavior. Swelling and shrinkage experiments revealed that cross-link density primarily governs the final equilibrium state but may also modulate the swelling and shrinkage rate under specific environmental conditions. To quantify this behavior, we introduce a novel parameter, the swelling/shrinkage affinity (<em>a</em><sub>sw</sub>, <em>a</em><sub>sh</sub>), which enables predictive evaluation of hydrogel responsiveness. The model integrates experimental data with rheological measurements, linking cross-link density to mechanical properties such as shear modulus. Rheological measurements validated the findings, correlating mechanical properties with cross-link density and aligning with swelling and shrinkage data. This work enhances the fundamental understanding of hydrogel behavior and offers a predictive tool for optimizing formulations in biomedical, environmental, and industrial applications. This framework may be extended in future work to incorporate external stimuli such as temperature or electromagnetic fields, potentially broadening the application of smart hydrogel systems.</div></div>","PeriodicalId":405,"journal":{"name":"Polymer","volume":"328 ","pages":"Article 128452"},"PeriodicalIF":4.1000,"publicationDate":"2025-04-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mathematical modeling of swelling and shrinking dynamics in pH-sensitive hydrogels composed of alginate, anionic cellulose, and chitosan\",\"authors\":\"Aleš Ručigaj, Tilen Kopač\",\"doi\":\"10.1016/j.polymer.2025.128452\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study develops a mathematical model to predict the swelling and shrinkage dynamics of pH-sensitive hydrogels composed of alginate, TEMPO-oxidized cellulose nanofibers (TOCNF), or chitosan. We investigated the effects of biopolymer type, cross-linking density, and/or pH conditions on hydrogel behavior. Swelling and shrinkage experiments revealed that cross-link density primarily governs the final equilibrium state but may also modulate the swelling and shrinkage rate under specific environmental conditions. To quantify this behavior, we introduce a novel parameter, the swelling/shrinkage affinity (<em>a</em><sub>sw</sub>, <em>a</em><sub>sh</sub>), which enables predictive evaluation of hydrogel responsiveness. The model integrates experimental data with rheological measurements, linking cross-link density to mechanical properties such as shear modulus. Rheological measurements validated the findings, correlating mechanical properties with cross-link density and aligning with swelling and shrinkage data. This work enhances the fundamental understanding of hydrogel behavior and offers a predictive tool for optimizing formulations in biomedical, environmental, and industrial applications. This framework may be extended in future work to incorporate external stimuli such as temperature or electromagnetic fields, potentially broadening the application of smart hydrogel systems.</div></div>\",\"PeriodicalId\":405,\"journal\":{\"name\":\"Polymer\",\"volume\":\"328 \",\"pages\":\"Article 128452\"},\"PeriodicalIF\":4.1000,\"publicationDate\":\"2025-04-24\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Polymer\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S0032386125004380\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"POLYMER SCIENCE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Polymer","FirstCategoryId":"92","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0032386125004380","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"POLYMER SCIENCE","Score":null,"Total":0}
Mathematical modeling of swelling and shrinking dynamics in pH-sensitive hydrogels composed of alginate, anionic cellulose, and chitosan
This study develops a mathematical model to predict the swelling and shrinkage dynamics of pH-sensitive hydrogels composed of alginate, TEMPO-oxidized cellulose nanofibers (TOCNF), or chitosan. We investigated the effects of biopolymer type, cross-linking density, and/or pH conditions on hydrogel behavior. Swelling and shrinkage experiments revealed that cross-link density primarily governs the final equilibrium state but may also modulate the swelling and shrinkage rate under specific environmental conditions. To quantify this behavior, we introduce a novel parameter, the swelling/shrinkage affinity (asw, ash), which enables predictive evaluation of hydrogel responsiveness. The model integrates experimental data with rheological measurements, linking cross-link density to mechanical properties such as shear modulus. Rheological measurements validated the findings, correlating mechanical properties with cross-link density and aligning with swelling and shrinkage data. This work enhances the fundamental understanding of hydrogel behavior and offers a predictive tool for optimizing formulations in biomedical, environmental, and industrial applications. This framework may be extended in future work to incorporate external stimuli such as temperature or electromagnetic fields, potentially broadening the application of smart hydrogel systems.
期刊介绍:
Polymer is an interdisciplinary journal dedicated to publishing innovative and significant advances in Polymer Physics, Chemistry and Technology. We welcome submissions on polymer hybrids, nanocomposites, characterisation and self-assembly. Polymer also publishes work on the technological application of polymers in energy and optoelectronics.
The main scope is covered but not limited to the following core areas:
Polymer Materials
Nanocomposites and hybrid nanomaterials
Polymer blends, films, fibres, networks and porous materials
Physical Characterization
Characterisation, modelling and simulation* of molecular and materials properties in bulk, solution, and thin films
Polymer Engineering
Advanced multiscale processing methods
Polymer Synthesis, Modification and Self-assembly
Including designer polymer architectures, mechanisms and kinetics, and supramolecular polymerization
Technological Applications
Polymers for energy generation and storage
Polymer membranes for separation technology
Polymers for opto- and microelectronics.