粘塑性
自愈水凝胶
材料科学
玻璃化转变
粘弹性
聚合物
应力松弛
复合材料
甲基丙烯酰胺
软化点
压力(语言学)
软化
放松(心理学)
甲基丙烯酸
高分子化学
蠕动
聚合
本构方程
热力学
共聚物
心理学
社会心理学
物理
丙烯酰胺
语言学
哲学
有限元法
作者
Baihong Chen,Xinning Zhang,Zi Liang Wu,Rui Xiao
出处
期刊:EPL
[Institute of Physics]
日期:2021-11-03
卷期号:139 (2): 26002-26002
标识
DOI:10.1209/0295-5075/ac35f6
摘要
Abstract Our recent works show that poly(methacrylamide- co -methacrylic acid) (P(MAAm- co -MAAc)) hydrogels with moderate water content (50–70 wt%) exhibit similar glass transition behaviours as in dry polymers. In the glassy state, these gels exhibit a modulus of several hundred megapascals and a failure strength of tens of megapascals, which are much higher than other reported tough gels. In this work, we apply a viscoplastic model to describe the temperature-dependent and rate-dependent mechanical behaviours of the P(MAAm- co -MAAc) gels. It is found that the viscoplastic model developed for dry polymers can also describe the stress-strain responses of gels including yielding and strain softening. It can also capture the stress relaxation behaviours. This work confirms that the glass transition in the gels and dry polymers shares a similar physical mechanism. Meanwhile, it indicates the classic viscoelastic/viscoplastic models can be readily applied for this new type of tough gels.
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