含有表面活性剂的剪切膜流的热毛细管不稳定性

IF 2.5 3区 物理与天体物理 Q2 PHYSICS, FLUIDS & PLASMAS
Arnab Choudhury, Arghya Samanta
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引用次数: 0

摘要

我们研究了当薄膜表面被不溶表面活性剂覆盖时,二维重力驱动剪切不可压缩粘性薄膜流过均匀加热斜壁时的线性热毛细管不稳定性。目的是将先前的研究[Wei,Phys. Fluids 17, 012103 (2005)]扩展到非等温粘性薄膜的情况。因此,能量方程与质量守恒和动量方程一起被纳入了控制方程。在本研究中,除了已知的 H 模式(表面模式)和表面活性剂模式之外,我们还发现了在低到中等雷诺数条件下的两种额外的热毛细管 S 模式和 P 模式。长波分析预测,表面活性剂马兰戈尼数(用于测量因不溶性表面活性剂浓度变化而产生的表面张力梯度)对 H 模式有稳定作用,而热马兰戈尼数(用于测量因温度变化而产生的表面张力梯度)则有破坏作用。这些相反的影响在它们之间产生了一种分析关系,即非等温膜流 H 模式不稳定的临界雷诺数与等温膜流的临界雷诺数相吻合。另一方面,数值结果表明,表面活性剂马兰戈尼数对热毛细管 S 模式和 P 模式具有稳定影响。更具体地说,这些热毛细管不稳定性随着表面活性剂马兰戈尼数的增加而减弱。然而,这些热毛细管不稳定性会随着热马兰戈尼数的增加而增强。此外,热马兰戈尼数会破坏表面活性剂模式不稳定性,但在存在热马兰戈尼数的情况下,不稳定性的发生并不受影响,这与表面活性剂马兰戈尼数对表面活性剂模式不稳定性发生的影响形成了鲜明对比。有趣的是,衡量热对流和热传导比率的比奥特数在表面活化剂模式不稳定性中显示出双重作用,尽管不稳定性阈值保持不变。在高雷诺数条件下,剪切模式出现,并通过表面活性剂马兰戈尼数而稳定,但通过热马兰戈尼数而失稳。此外,有惯性和无惯性结果的比较表明,惯性对表面活性剂模式起稳定作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Thermocapillary instability of a surfactant-laden shear-imposed film flow

Thermocapillary instability of a surfactant-laden shear-imposed film flow
We examine the linear thermocapillary instability of a two-dimensional gravity-driven shear-imposed incompressible viscous film flowing over a uniformly heated inclined wall when the film surface is covered by an insoluble surfactant. The aim is to expand the prior research [Wei, Phys. Fluids 17, 012103 (2005)] to the case of a nonisothermal viscous film. As a result, the energy equation is incorporated into the governing equations along with the mass conservation and momentum equations. In the present study, we have found two additional thermocapillary S- and P-modes in the low to moderate Reynolds number regime, along with the known H-mode (surface mode) and surfactant mode. The long-wave analysis predicts that the surfactant Marangoni number, which measures the surface tension gradient due to a change in insoluble surfactant concentration, has a stabilizing impact on the H-mode, but the thermal Marangoni number, which measures the surface tension gradient due to a change in temperature, has a destabilizing impact. These opposing effects produce an analytical relationship between them for which the critical Reynolds number for the H-mode instability of the nonisothermal film flow coincides with that of the isothermal film flow. On the other hand, the numerical result exhibits that the surfactant Marangoni number has a stabilizing influence on the thermocapillary S-mode and P-mode. More specifically, these thermocapillary instabilities diminish with an increase in the value of the surfactant Marangoni number. However, these thermocapillary instabilities can be made stronger by increasing the value of the thermal Marangoni number. Furthermore, the thermal Marangoni number destabilizes the surfactant mode instability, but the onset of instability is not affected in the presence of the thermal Marangoni number, which is in contrast to the influence of the surfactant Marangoni number on the onset of surfactant mode instability. Interestingly, the Biot number, which measures the ratio of heat convection and heat conduction, shows a dual role in the surfactant mode instability, even though the threshold of instability remains the same. In the high Reynolds number regime, the shear mode appears and is stabilized by the surfactant Marangoni number but destabilized by the thermal Marangoni number. Moreover, the comparison of results with inertia and without inertia exhibits a stabilizing role of inertia in the surfactant mode.
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来源期刊
Physical Review Fluids
Physical Review Fluids Chemical Engineering-Fluid Flow and Transfer Processes
CiteScore
5.10
自引率
11.10%
发文量
488
期刊介绍: Physical Review Fluids is APS’s newest online-only journal dedicated to publishing innovative research that will significantly advance the fundamental understanding of fluid dynamics. Physical Review Fluids expands the scope of the APS journals to include additional areas of fluid dynamics research, complements the existing Physical Review collection, and maintains the same quality and reputation that authors and subscribers expect from APS. The journal is published with the endorsement of the APS Division of Fluid Dynamics.
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