材料科学
明胶
双层
执行机构
离子强度
离子键合
甲基丙烯酸酯
自愈水凝胶
复合材料
离子液体
图层(电子)
化学工程
生物高聚物
膜
纳米技术
人工肌肉
聚合物
高分子化学
水溶液
离子
化学
共聚物
计算机科学
催化作用
有机化学
人工智能
工程类
生物化学
作者
Shengzhu Zhou,Baoyi Wu,Qiang Zhou,Yukun Jian,Xiaoxia Le,Huanhuan Lu,Dachuan Zhang,Jiawei Zhang,Zhihui Zhang,Tao Chen
标识
DOI:10.1002/marc.201900543
摘要
Abstract As one of the most promising intelligent materials, polymeric hydrogel actuators could produce reversible shape change upon external stimuli. Although complex shape deformation from 2D to 3D have been achieved, the realization of actuating behavior from 3D to 3D is still a significant challenge. Herein, an effective strategy to develop a novel bilayer hollow spherical hydrogel actuator is proposed. Through immersing a Ca 2+ incorporated gelatin core into alginate solution, an ionic‐strength‐responsive alginate layer will be formed along the gelatin core via alginate–Ca 2+ crosslinks, and then another thermo‐responsive alginate‐poly(2‐(dimethylamino)ethyl methacrylate)(Alg‐PDMAEMA) layer is introduced to achieve a bilayer hydrogel with ionic strength and temperature dual responsiveness. A hollow hydrogel capsule could be obtained if a spherical gelatin core is applied, and it could produce complex shape deformations from 3D to 3D upon the trigger of ionic strength and temperatures changes. The present work may offer new inspirations for the development of novel intelligent polymeric hydrogel actuators.
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