论文标题

在流场存在下,能量polydisperse 2d Lennard-Jones流体

Energy polydisperse 2d Lennard-Jones fluid in presence of flow field

论文作者

Shagolsem, Lenin S.

论文摘要

使用分子动力学模拟,研究了能量多分散$ 2D $ LENNARD-JONES流体(以薄膜几何形状)进行线性流场的行为。通过考虑中性和选择性底物,我们系统地探讨了流场对粒子排序以及系统响应的影响。结果表明,膜密度曲线,空间组织以及膜中的局部粒子身份排序受到影响。此外,我们观察到与有效交互参数减少相关的流场感应熔点,$ \ left <ε_i^{\ rm eff} \ right> $,这表征了本地邻域身份排序。在宏观反应方面,该系统既显示剪切粉化和剪切厚的行为,并且剪切薄的指数随着温度的升高而降低,并最终在足够高的温度下达到了Netwonian流体样行为。发现一个成分LJ富流体和具有中性底物的能量多分散流体的定性行为在许多方面都是相似的,而具有选择性底物的一种质子却显示出差异。在能量多分散系统的情况下,具有不同底物类型的效果在接口附近的密度曲线中显着表现出来,$ \ left <ε_i^{\ rm eff} \ right> $,以及粘度。我们已经表明,与一种组分流体不同,可以通过调整能量多分散流体中的底物 - 流体相互作用来调整宏观响应。

The behavior of energy polydisperse $2d$ Lennard-Jones fluid (in thin-film geometry) is studied subjected to linear flow field using molecular dynamics simulations. By considering neutral and selective substrates we systematically explore the effect of flow field on particle ordering as well as response of the system. It is shown that particle density profile, spatial organization as well as local particle identity ordering in the film are affected. Furthermore, we observe flow field induced melting associated with a decrease of effective interaction parameter, $\left< ε_i^{\rm eff} \right>$, which characterizes local neighborhood identity ordering. In terms of macroscopic response, the systems show both shear-thinning and shear-thickening behaviors, and shear-thinning exponent decreases with increasing temperature and eventually attains Netwonian fluid-like behavior at sufficiently high temperature. It is found that the qualitative behaviour of one component LJ-fluid and energy polydisperse fluid with neutral substrates are similar in many respects, while the one with selective substrate shows differences. In the case of energy polydisperse system, the effect of having different substrate types is significantly manifested in the density profile near the interface, $\left< ε_i^{\rm eff} \right>$, and in the viscosity. We have shown that, unlike one component fluid, it is possible to tune the macroscopic response by tuning substrate-fluid interaction in energy polydisperse fluids.

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