自愈水凝胶
褐藻酸
流变学
水溶液
纤维
化学工程
刚度
软物质
化学
材料科学
松弛法
弹性(物理)
高分子化学
复合材料
磁共振成像
有机化学
自旋回波
放射科
工程类
医学
胶体
生物化学
作者
M. P. Nakada,Hiroyuki Ishida,Hironobu UCHIYAMA,Rena Ota,Toshihiko Ogura,Yusuke Namiki
标识
DOI:10.1016/j.ijbiomac.2024.131890
摘要
The rheological and morphological characteristics of Ca-crosslinked alginate hydrogels with two different M/G ratios, α-L-guluronate (G)-rich and β-D-mannuronate (M)-rich, each with one alginic acid concentration, were investigated. It was found that the stiffness and elasticity of alginate hydrogels are derived from the thickness and density of the fibril network structures. In aqueous alginate solution, ball-like aggregates of alginates are present. Time-resolved small-angle X-ray scattering and time-domain nuclear magnetic resonance measurements suggest that the disaggregation of alginate aggregates and loose fibrillation occur in the early stage of the sol-gel transition. After these induction stage, direct gelation is finally caused by the formation of the egg-box junction. G-rich alginate hydrogel has a higher stiffness and a thicker and denser fibril network structure than M-rich alginate hydrogel. The former also exhibits faster and more significant changes in physical properties during the sol-gel transition.
科研通智能强力驱动
Strongly Powered by AbleSci AI