M.H. Wolf , N. Izaguirre , J. Labidi , A. Ribes-Greus
{"title":"戊二醛或庚尼平交联壳聚糖膜的介电性能","authors":"M.H. Wolf , N. Izaguirre , J. Labidi , A. Ribes-Greus","doi":"10.1016/j.reactfunctpolym.2025.106271","DOIUrl":null,"url":null,"abstract":"<div><div>This study investigates the impact of covalent cross-linking using glutaraldehyde (GA) and the biobased alternative genipin (GP) on the dielectric and conductive properties of chitosan membranes. For protonation, the solvent-casted membranes were immersed in a 1.0 M sulfuric acid solution (S). The resulting property changes were assessed using Fourier-Transform Infrared (FTIR) spectroscopy, water uptake studies, Differential Scanning Calorimetry (DSC), and Dielectric Thermal Analysis (DETA). The genipin-cross-linked membrane demonstrated higher water uptake than the glutaraldehyde-cross-linked one, attributed to less effective cross-linking and greater free volume between polymer chains. The membranes immersed in the sulfuric acid solution exhibited reduced water uptake and swelling due to a denser structure formed by short ionic bridges. All the chitosan-based materials showed dielectric spectra containing the same relaxation mechanisms (β-, β<sub>wet</sub>-, α-relaxation, and MWS polarisation). Covalent cross-linking and sulfuric acid immersion increased the activation energy of the β-relaxation, due to the formation of strong bonds that limit the mobility of glycosidic linkages. The covalent bonds restrict the segmental dynamics of the chitosan backbone, leading to an increase in the Vogel temperature of the associated α-relaxation, particularly with glutaraldehyde. The β<sub>wet</sub>-relaxation temperature decreased following sulfuric acid solution treatment, due to greater retention of bound water resulting from the incorporation of charged sulfate groups.</div></div>","PeriodicalId":20916,"journal":{"name":"Reactive & Functional Polymers","volume":"213 ","pages":"Article 106271"},"PeriodicalIF":4.5000,"publicationDate":"2025-03-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Dielectric properties of chitosan membranes cross-linked with glutaraldehyde or genipin\",\"authors\":\"M.H. Wolf , N. Izaguirre , J. Labidi , A. Ribes-Greus\",\"doi\":\"10.1016/j.reactfunctpolym.2025.106271\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>This study investigates the impact of covalent cross-linking using glutaraldehyde (GA) and the biobased alternative genipin (GP) on the dielectric and conductive properties of chitosan membranes. For protonation, the solvent-casted membranes were immersed in a 1.0 M sulfuric acid solution (S). The resulting property changes were assessed using Fourier-Transform Infrared (FTIR) spectroscopy, water uptake studies, Differential Scanning Calorimetry (DSC), and Dielectric Thermal Analysis (DETA). The genipin-cross-linked membrane demonstrated higher water uptake than the glutaraldehyde-cross-linked one, attributed to less effective cross-linking and greater free volume between polymer chains. The membranes immersed in the sulfuric acid solution exhibited reduced water uptake and swelling due to a denser structure formed by short ionic bridges. All the chitosan-based materials showed dielectric spectra containing the same relaxation mechanisms (β-, β<sub>wet</sub>-, α-relaxation, and MWS polarisation). Covalent cross-linking and sulfuric acid immersion increased the activation energy of the β-relaxation, due to the formation of strong bonds that limit the mobility of glycosidic linkages. The covalent bonds restrict the segmental dynamics of the chitosan backbone, leading to an increase in the Vogel temperature of the associated α-relaxation, particularly with glutaraldehyde. The β<sub>wet</sub>-relaxation temperature decreased following sulfuric acid solution treatment, due to greater retention of bound water resulting from the incorporation of charged sulfate groups.</div></div>\",\"PeriodicalId\":20916,\"journal\":{\"name\":\"Reactive & Functional Polymers\",\"volume\":\"213 \",\"pages\":\"Article 106271\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2025-03-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Reactive & Functional Polymers\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1381514825001233\",\"RegionNum\":3,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, APPLIED\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Reactive & Functional Polymers","FirstCategoryId":"5","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1381514825001233","RegionNum":3,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, APPLIED","Score":null,"Total":0}
Dielectric properties of chitosan membranes cross-linked with glutaraldehyde or genipin
This study investigates the impact of covalent cross-linking using glutaraldehyde (GA) and the biobased alternative genipin (GP) on the dielectric and conductive properties of chitosan membranes. For protonation, the solvent-casted membranes were immersed in a 1.0 M sulfuric acid solution (S). The resulting property changes were assessed using Fourier-Transform Infrared (FTIR) spectroscopy, water uptake studies, Differential Scanning Calorimetry (DSC), and Dielectric Thermal Analysis (DETA). The genipin-cross-linked membrane demonstrated higher water uptake than the glutaraldehyde-cross-linked one, attributed to less effective cross-linking and greater free volume between polymer chains. The membranes immersed in the sulfuric acid solution exhibited reduced water uptake and swelling due to a denser structure formed by short ionic bridges. All the chitosan-based materials showed dielectric spectra containing the same relaxation mechanisms (β-, βwet-, α-relaxation, and MWS polarisation). Covalent cross-linking and sulfuric acid immersion increased the activation energy of the β-relaxation, due to the formation of strong bonds that limit the mobility of glycosidic linkages. The covalent bonds restrict the segmental dynamics of the chitosan backbone, leading to an increase in the Vogel temperature of the associated α-relaxation, particularly with glutaraldehyde. The βwet-relaxation temperature decreased following sulfuric acid solution treatment, due to greater retention of bound water resulting from the incorporation of charged sulfate groups.
期刊介绍:
Reactive & Functional Polymers provides a forum to disseminate original ideas, concepts and developments in the science and technology of polymers with functional groups, which impart specific chemical reactivity or physical, chemical, structural, biological, and pharmacological functionality. The scope covers organic polymers, acting for instance as reagents, catalysts, templates, ion-exchangers, selective sorbents, chelating or antimicrobial agents, drug carriers, sensors, membranes, and hydrogels. This also includes reactive cross-linkable prepolymers and high-performance thermosetting polymers, natural or degradable polymers, conducting polymers, and porous polymers.
Original research articles must contain thorough molecular and material characterization data on synthesis of the above polymers in combination with their applications. Applications include but are not limited to catalysis, water or effluent treatment, separations and recovery, electronics and information storage, energy conversion, encapsulation, or adhesion.