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Acid-Induced Gelation of Carboxymethylcellulose Solutions

Gauthier LegrandENSL, CNRS, Laboratoire de Physique, F-69342 Lyon, FranceGuilhem P. BaezaUniv Lyon, INSA Lyon, UCBL, CNRS, MATEIS, UMR5510, 69621 Villeurbanne, FranceMatteo PeylaENSL, CNRS, Laboratoire de Physique, F-69342 Lyon, FranceLionel PorcarInstitut Laue Langevin, 38000 Grenoble, FranceCarlos Fernández‐de‐AlbaUniversité de Lyon, CNRS, Université Claude Bernard Lyon 1, INSA Lyon, Université Jean Monnet, UMR 5223, Ingénierie des Matériaux Polymères, Service RMN Polymères de l’ICL, F-69621 Cédex, FranceSébastien MannevilleENSL, CNRS, Laboratoire de Physique, F-69342 Lyon, FranceThibaut DivouxENSL, CNRS, Laboratoire de Physique, F-69342 Lyon, France
2024en
ABI

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The present work offers a comprehensive description of the acid-induced gelation of carboxymethylcellulose (CMC), a water-soluble derivative of cellulose broadly used in numerous applications ranging from food packaging to biomedical engineering. Linear viscoelastic properties measured at various pH and CMC contents allow us to build a sol-gel phase diagram and show that CMC gels exhibit broad power-law viscoelastic spectra that can be rescaled onto a master curve following a time-composition superposition principle. These results demonstrate the microstructural self-similarity of CMC gels and inspire a mean-field model based on hydrophobic interchain association that accounts for the sol-gel boundary over the entire range of CMC content under study. Neutron scattering experiments further confirm this picture and suggest that CMC gels comprise a fibrous network cross-linked by aggregates. Finally, low-field NMR measurements offer an original signature of acid-induced gelation from a solvent perspective. Altogether, these results open avenues for the precise manipulation and control of CMC-based hydrogels.

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