Thixo-elastoviscoplastic modeling of human blood

A. Spyridakis, P. Moschopoulos, S. Varchanis, Y. Dimakopoulos, J. Tsamopoulos
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Abstract

We propose an enhanced model for the rheological characterization of human blood that accounts for thixotropy, viscoelasticity, and yield-stress. Blood plasma is assumed to act as a Newtonian solvent. We introduce a scalar variable, λ, to macroscopically describe the structure of blood. The temporal evolution of λ is governed by an equation that accounts for aggregation of red blood cells and breakdown of rouleaux structures. We introduce a Gaussian function that qualitatively describes experimental findings on rouleaux restructuring and the expression that was proposed by Stephanou and Georgiou for the breakdown term. The constitutive equation for stresses is based on the elastoviscoplastic formalism by Saramito. However, the max term of the viscoplastic deformation rate has been replaced by a continuous function of λ to account for smooth solid-fluid transition, following the experimental evidence. The continuous yielding description provides improved rheological predictions, especially in small amplitude oscillatory shear. The model predicts finite viscous dissipation at small amplitude oscillation, as we would expect from a gel material-like human blood. Overall, it has nine adjustable parameters that are fitted simultaneously to experimental data by nonlinear regression. The model can accurately predict numerous flow conditions: steady shear, step shear, hysteresis loops, and oscillatory shear. We compare this model (TEVP 9) to our previous formulation for human blood (TEVP 11), and we show that the predictions of the new model are more accurate, despite using fewer parameters. We provide additional predictions for uniaxial elongation, which include finite normal stress difference, extensional hardening at large values of the extensional rate, and extensional thinning at extremely large extensional rates.
人体血液的硫氧弹性塑性模型
我们提出了一种用于描述人体血液流变特性的增强模型,该模型考虑了触变性、粘弹性和屈服应力。血浆被假定为牛顿溶剂。我们引入一个标量变量 λ 来宏观描述血液的结构。λ 的时间演变受一个方程控制,该方程考虑了红细胞的聚集和胭脂虫结构的破坏。我们引入了一个高斯函数,该函数定性地描述了关于胭脂虫结构重组的实验结果,以及 Stephanou 和 Georgiou 提出的分解项表达式。应力的构成方程基于萨拉米托的弹性粘塑性形式主义。不过,粘塑性变形率的最大项已被 λ 的连续函数所取代,以便根据实验证据解释平稳的固-流过渡。连续屈服描述改进了流变预测,特别是在小振幅振荡剪切中。该模型预测了小振幅振荡时的有限粘性耗散,正如我们对类似人体血液的凝胶材料所期望的那样。总体而言,该模型有九个可调参数,通过非线性回归与实验数据同时拟合。该模型可以准确预测多种流动条件:稳定剪切、阶跃剪切、滞后环和振荡剪切。我们将该模型(TEVP 9)与之前的人体血液模型(TEVP 11)进行了比较,结果表明,尽管使用的参数较少,但新模型的预测结果更为准确。我们为单轴伸长提供了额外的预测,其中包括有限法向应力差、大伸长率值下的伸长硬化以及超大伸长率下的伸长变薄。
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