自愈水凝胶
材料科学
明胶
结块
粘弹性
流变学
复合材料
离子键合
剪切模量
剪切(地质)
离子强度
化学工程
高分子化学
水溶液
化学
物理化学
离子
生物化学
有机化学
工程类
作者
Thomas B. Goudoulas,Anna Didonaki,Sharadwata Pan,Ehsan Fattahi,Thomas Becker
出处
期刊:Polymers
[MDPI AG]
日期:2023-03-21
卷期号:15 (6): 1558-1558
被引量:5
标识
DOI:10.3390/polym15061558
摘要
Hydrogels are highly versatile and widely applicable materials within various scientific, technological, and food sectors. Alginate and gelatin hydrogels, along with their crafted variations, are possibly the most common ones. However, the ionic crosslinking of alginate-Ca++ is a different gelation mechanism than the physical crosslinking of gelatin. In this work, we prepare alginate-Ca++ hydrogels using individual layer gelation and experimentally evaluate LAOS rheological behavior. We apply shear-stress decomposition using the MITlaos software and obtain the elastic and viscous contributions within the nonlinear response of the individual alginate-Ca++ layer. We compare these results with the nonlinear responses of the gelatin-alginate ex situ individual layer. The strain-sweep patterns are similar, with loss modulus overshoot. The applied shear can destroy the larger-scale structural units (agglomerate/aggregates), resulting in analogous patterns. However, the critical strain points are different. Based on the shear-thickening ratio T of the LAOS analysis, it can be assumed that the common feature of ex situ preparation, i.e., gelation as individual layers, provides a matching bulk microstructure, as the hydrogels differ significantly at a molecular-binding level.
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