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Renormalized Flory-Huggins lattice model of physicochemical kinetics and dynamic complexity in self-healing double-network hydrogel

机译:一种重型化的麦克风 - Huggins物理化学动力学与自愈双网络水凝凝血动态复杂性的晶格模型

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摘要

Self-healing capability offers great designability on mechanical properties of double-network (DN) hydrogel. However, the thermodynamics understanding behind such physicochemical transitions and self-healing behaviors are yet to be explored properly. This study describes a renormalized Flory-Huggins lattice model for DN hydrogels, of which the physicochemical kinetics and dynamic complexity are resulted from stress-induced bond scission and macromolecule rearrangement. Based on the Flory-Huggins lattice model and Gaussian distribution theory, an extended free-energy model was formulated by the steric repulsive free-energy function. Afterwards, the function was used to identify the working mechanisms and thermodynamics in self-healing DN hydrogels with ultra-high mechanical strength. Finally, the effectiveness of model was demonstrated by applying it to predict the mechanical behaviors of DN hydrogels, where the analytical results showed good agreements with experiment data.
机译:自愈合能力为双网络(DN)水凝胶的机械性能提供了极大的可设计性。然而,对这种物理化学转变和自愈行为背后的热力学理解尚待充分探索。本研究描述了DN水凝胶的重正化Flory-Huggins晶格模型,其物理化学动力学和动力学复杂性是由应力诱导的键断裂和大分子重排引起的。基于Flory-Huggins晶格模型和高斯分布理论,利用空间排斥自由能函数建立了一个扩展的自由能模型。之后,利用该函数确定了具有超高机械强度的自修复DN水凝胶的工作机理和热力学。最后,将该模型应用于DN水凝胶的力学行为预测,分析结果与实验数据吻合良好,证明了该模型的有效性。

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