液滴粘度比和表面活性剂吸附对具有界面粘度的液滴凝聚的影响

Fluids Pub Date : 2024-02-13 DOI:10.3390/fluids9020048
Natasha Singh, V. Narsimhan
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引用次数: 0

摘要

对于吸附了蛋白质、固体颗粒、脂质或聚合物的液滴来说,表面流变学变得非常重要,而了解表面流变学如何改变凝聚等基本液滴过程,有助于深入了解工业和生物系统中分散液的处理过程。在这项研究中,我们模拟了在斯托克斯流动极限的轴对称双轴伸展流动条件下,两个大小相等的可变形液滴的接近过程。我们探讨了当存在界面粘度时,液滴和悬浮液之间的粘度对比如何改变薄膜的排水行为。对于毛细管数固定的干净液滴,在 λ≤O(1) 时,观察到排水时间与粘度比 (λ) 无关,而在λ≥O(1) 时,排水时间随粘度比线性增加。表面粘度使液滴之间的薄膜变平变宽,从而增加了排水时间,并使粘度比发生变化,在此粘度比上,上述缩放行为变为较大值。与较高的粘度比值相比,较低的粘度比值会更明显地延长排水时间。在本文的后半部分,我们研究了当表面活性剂可溶解时,表面粘度如何改变薄膜排水。我们研究了动力学控制的吸附/解吸极限。我们发现,表面活性剂的可溶性消除了表面张力梯度,增加了表面粘度效应的显著性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Effect of Droplet Viscosity Ratio and Surfactant Adsorption on the Coalescence of Droplets with Interfacial Viscosity
Surface rheology becomes important for droplets with adsorbed proteins, solid particulates, lipids, or polymers, and understanding how surface rheology alters basic droplet processes like coalescence provides insight into the processing of dispersions in industrial and biological systems. In this work, we model the approach of two equal-size deformable droplets under an axisymmetric, biaxial extensional flow in the Stokes flow limit. We explore how the viscosity contrast between the drop and suspending fluid alters the film drainage behaviour when interfacial viscosity is present. For a clean droplet at a fixed capillary number, the drainage time is observed to be independent of the viscosity ratio (λ) for λ≤O(1), while the drainage increases linearly with the viscosity ratio for λ≥O(1). Surface viscosity increases the drainage time by causing the thin film between the droplets to flatten and widen, and shifts the viscosity ratio at which the aforementioned scaling behaviour changes to larger values. The drainage time is increased more significantly at lower viscosity ratio values than higher values. In the second half of the paper, we examine how surface viscosity alters film drainage when the surfactant can be soluble. We examine the kinetically controlled adsorption/desorption limit. We find that surfactant solubility abolishes surface tension gradients and increases the prominence of surface viscosity effects, the effects of which are quantified for Boussinesq numbers Bq∼O(0.1).
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