A 2D Geometrical Perspective for the Contact Angle Hysteresis.

IF 3.9 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Lei Liu,Guanlong Guo,Kaiyu Wang,Linke Chen,Yangyang Fan,Sergio Andres Galindo Torres,Jiu-An Lv,Herbert E Huppert,Changfu Wei,Liang Lei
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引用次数: 0

Abstract

Contact angle and its hysteresis during advancing and receding are probably the most fundamental concepts when two fluids interact with a solid surface. Surface roughness/microstructure affects contact angle hysteresis. Fiber is a common structure used to fabricate functional surfaces. However, a general model for fiber rough surfaces has not been obtained. This work, from a geometrical perspective, derives analytical solutions for the relationships between droplet volume and apparent contact angles and asymptotes for advancing, receding, and equilibrium contact angles on the surface with cylindrical humps. Energy evolution is tracked by calculating the Gibbs free interfacial energy. Results show that the contact angle hysteresis is constrained by geometry when assumptions are met. The advancing, receding, and equilibrium contact angles oscillate and gradually approach the predicted asymptote values with increasing humps. Gibbs free interfacial energy drops upon droplet advancing and receding. This energy cliff would induce droplet vibration, and the energy can be dissipated via fluid internal friction. Lattice Boltzmann method (LBM) simulations and quasi-2D experiments verify these solutions and demonstrate dynamic behaviors during droplet jumps to the next hump. From an energy perspective, the equilibrium contact angle can fall outside the contact angle hysteresis, although geometrically impossible. Energy analysis reveals that the Gibbs free energy at 0° can be order-of-magnitude less than that at other apparent contact angles. 3D experiments confirm that prewetted rough surfaces can reach this more stable configuration devoid of contact angle hysteresis, verifying 2D analytical modeling. Note that the theoretical analysis is based on idealistic assumptions, and the real circumstance may deviate from these assumptions.
接触角迟滞的二维几何透视。
当两种流体与固体表面相互作用时,接触角及其在前进和后退过程中的滞后可能是最基本的概念。表面粗糙度/微观结构影响接触角滞后。纤维是用于制造功能表面的常用结构。然而,纤维粗糙表面的一般模型尚未得到。本文从几何角度出发,推导出液滴体积与表观接触角之间关系的解析解,以及具有圆柱形凸起的表面上推进、后退和平衡接触角的渐近线的解析解。通过计算吉布斯自由界面能来跟踪能量演化。结果表明,在满足假设条件下,接触角迟滞受几何约束。前进,后退和平衡接触角振荡并逐渐接近预测的渐近线值,并增加驼峰。吉布斯自由界面能随液滴前进和后退而下降。这种能量悬崖会引起液滴振动,能量可以通过流体内摩擦耗散。晶格玻尔兹曼方法(LBM)模拟和准二维实验验证了这些解,并演示了液滴跳到下一个峰时的动态行为。从能量的角度来看,平衡接触角可以落在接触角迟滞之外,尽管几何上不可能。能量分析表明,在0°处的吉布斯自由能比在其他视接触角处的吉布斯自由能小一个数量级。三维实验证实,预湿粗糙表面可以达到这种更稳定的结构,没有接触角滞后,验证了二维分析模型。请注意,理论分析是基于理想主义的假设,实际情况可能会偏离这些假设。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Langmuir
Langmuir 化学-材料科学:综合
CiteScore
6.50
自引率
10.30%
发文量
1464
审稿时长
2.1 months
期刊介绍: Langmuir is an interdisciplinary journal publishing articles in the following subject categories: Colloids: surfactants and self-assembly, dispersions, emulsions, foams Interfaces: adsorption, reactions, films, forces Biological Interfaces: biocolloids, biomolecular and biomimetic materials Materials: nano- and mesostructured materials, polymers, gels, liquid crystals Electrochemistry: interfacial charge transfer, charge transport, electrocatalysis, electrokinetic phenomena, bioelectrochemistry Devices and Applications: sensors, fluidics, patterning, catalysis, photonic crystals However, when high-impact, original work is submitted that does not fit within the above categories, decisions to accept or decline such papers will be based on one criteria: What Would Irving Do? Langmuir ranks #2 in citations out of 136 journals in the category of Physical Chemistry with 113,157 total citations. The journal received an Impact Factor of 4.384*. This journal is also indexed in the categories of Materials Science (ranked #1) and Multidisciplinary Chemistry (ranked #5).
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