宾月珍

个人信息Personal Information

教授

博士生导师

硕士生导师

性别:女

毕业院校:奈良女子大学

学位:博士

所在单位:化工学院

学科:高分子材料. 高分子化学与物理

办公地点:大连理工大学西部校区知顺楼A203

联系方式:0411-84986093

电子邮箱:binyz@dlut.edu.cn

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Elastic-Plastic Transformation of Polyelectrolyte Complex Hydrogels from Chitosan and Sodium Hyaluronate

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论文类型:期刊论文

发表时间:2018-11-13

发表刊物:MACROMOLECULES

收录刊物:SCIE、Scopus

卷号:51

期号:21

页面范围:8887-8898

ISSN号:0024-9297

关键字:Biomolecules; Biopolymers; Chitosan; Elastoplasticity; Hyaluronic acid; Hydrogels; Hysteresis; Ionic strength; Polyelectrolytes; Sodium; Stress relaxation; Tensile strain; Tensile testing; Yield stress, Charge composition; Cyclic tensile tests; Mechanical behavior; Negatively charged; Polyelectrolyte complexation; Polyelectrolyte complexes; Strain and strain rates; Synthetic polyelectrolyte, Strain rate

摘要:Hydrogels formed by polyelectrolyte complexation (PEC) of oppositely charged biopolymers, free of any chemical additives, are promising biomaterials. In this work, the mechanical behavior of hydrogels consisting of positively charged chitosan and negatively charged sodium hyaluronate (HA) at balanced charge composition is investigated. These hydrogels exhibit strong tensile strain and strain rate dependence. They are elastic-like, independent of the strain rate at small strain, but exhibit plastic-like behavior above the yield point by showing a monotonous decrease of the stress. The cyclic tensile test demonstrates that these hydrogels exhibit small and quickly recoverable hysteresis in the elastic-like region but large and partially recoverable hysteresis above the yield point. The stress relaxation experiment shows a plateau in the reduced stress followed by an abrupt fracture, and the time to failure decreases exponentially with increasing applied step strain. Such elastic-to-plastic-like transformation of the biopolymer PEC gels is quite different from the behaviors of PEC hydrogels formed by oppositely charged vinyl-type synthetic polyelectrolytes due to the difference in flexibility, charge density, and ionic bond strength of these polymers.