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半柔性聚合物水凝胶中的正应力。

Normal stresses in semiflexible polymer hydrogels.

作者信息

Vahabi M, Vos Bart E, de Cagny Henri C G, Bonn Daniel, Koenderink Gijsje H, MacKintosh F C

机构信息

Department of Physics and Astronomy, Vrije Universiteit, Amsterdam, The Netherlands.

AMOLF, Department of Living Matter, 1098 XG Amsterdam.

出版信息

Phys Rev E. 2018 Mar;97(3-1):032418. doi: 10.1103/PhysRevE.97.032418.

Abstract

Biopolymer gels such as fibrin and collagen networks are known to develop tensile axial stress when subject to torsion. This negative normal stress is opposite to the classical Poynting effect observed for most elastic solids including synthetic polymer gels, where torsion provokes a positive normal stress. As shown recently, this anomalous behavior in fibrin gels depends on the open, porous network structure of biopolymer gels, which facilitates interstitial fluid flow during shear and can be described by a phenomenological two-fluid model with viscous coupling between network and solvent. Here we extend this model and develop a microscopic model for the individual diagonal components of the stress tensor that determine the axial response of semiflexible polymer hydrogels. This microscopic model predicts that the magnitude of these stress components depends inversely on the characteristic strain for the onset of nonlinear shear stress, which we confirm experimentally by shear rheometry on fibrin gels. Moreover, our model predicts a transient behavior of the normal stress, which is in excellent agreement with the full time-dependent normal stress we measure.

摘要

众所周知,诸如纤维蛋白和胶原蛋白网络等生物聚合物凝胶在受到扭转时会产生拉伸轴向应力。这种负向正应力与在包括合成聚合物凝胶在内的大多数弹性固体中观察到的经典泊松效应相反,在经典泊松效应中,扭转会引发正向正应力。最近的研究表明,纤维蛋白凝胶中的这种异常行为取决于生物聚合物凝胶开放的多孔网络结构,这种结构有利于剪切过程中的间质液流动,并且可以用一个网络与溶剂之间存在粘性耦合的唯象双流体模型来描述。在此,我们扩展了该模型,并针对决定半柔性聚合物水凝胶轴向响应的应力张量的各个对角分量开发了一个微观模型。这个微观模型预测,这些应力分量的大小与非线性剪切应力开始时的特征应变成反比,我们通过对纤维蛋白凝胶进行剪切流变学实验证实了这一点。此外,我们的模型预测了正应力的瞬态行为,这与我们测量的随时间变化的完整正应力非常吻合。

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