Probing metal-carboxylate interactions in cellulose nanofibrils-based hydrogels using nonlinear oscillatory rheology

被引:11
作者
Song, Yeeun [1 ]
Kim, Bogyoung [1 ]
Park, Jun Dong [2 ]
Lee, Doojin [1 ]
机构
[1] Chonnam Natl Univ, Dept Polymer Sci & Engn, Gwangju 61186, South Korea
[2] Sookmyung Womens Univ, Dept Chem & Biol Engn, Seoul 04310, South Korea
基金
新加坡国家研究基金会;
关键词
Cellulose nanofibrils; Hydrogels; Metal cation-carboxylate coordination bonding; Nonlinear viscoelasticity; Rheology; FOURIER-TRANSFORM RHEOLOGY; POLYMER NANOCOMPOSITES; SHEAR; VISCOELASTICITY; NANOCRYSTALS; DISPERSION; DYNAMICS; BEHAVIOR; NETWORK; BLENDS;
D O I
10.1016/j.carbpol.2022.120262
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
Cellulose nanofibrils (CNFs) have gained much attention as part of biocompatible soft hydrogels used in various biomedical applications such as biodegradable scaffolds, biomedicine, tissues, and regenerative medicine. The CNF hydrogels were mediated with metal cations for improved mechanical strength and structural reversibility. Intermolecular interactions in these CNF hydrogels are controlled by metal cation-carboxylate coordination bonding, leading to the creation of interconnected three-dimensional nanofibril structures that produce high structural reversibility. The nonlinear inter- and intra-cycle were investigated viscoelastic responses of these CNF hydrogels by quantitative nonlinear viscoelastic parameters and transient responses. The dynamic and transitional analyses conducted indicate that the structural deformation and recovery characteristics of the CNF hydrogels are affected by the valency number of the metal cations. This property can be carefully chosen to tune the intermolecular interactions between the cellulose nanofibrils to create an efficient interwoven network structure with high structural reversibility that can go through repeated cycles of reformation and yielding.
引用
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页数:9
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