Cohesive properties of thin films of liquids adhering to a solid surface

J. F. Padday
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引用次数: 63

Abstract

The process of forming and rupturing a thin liquid film at a solid surface is described thermodynamically for both high and low energy solid surfaces. In part 1 the build-up of thin films on high-energy surfaces from the first monolayer is considered and reviewed. Components of the surface free energy of formation of the thin film (disjoining pressure) are defined. For curved surfaces the disjoining forces should be combined with the Laplace capillary pressure to give a correct form of the Kelvin equation. It is suggested from the early work of Bangham and Deryaguin that thin liquid layers have anomalous physical properties. These studies are discussed in relation to the thickness of the liquid films.In part 2, new experimental evidence of the critical rupture thickness of thin liquid films on low energy surface is presented. A number of pure liquids rupture spontaneously on low energy surfaces such as wax or polytetrafluoroethylene at very great thicknesses (0.01 cm). The effects of aqueous salt and surfactant solutions suggest these long-range forces are electrical in origin.
液体薄膜附着在固体表面上的粘合特性
本文描述了在固体表面形成和破裂液体薄膜的过程,包括高能和低能固体表面。在第一部分中,考虑并回顾了从第一层单层在高能表面上形成薄膜的过程。定义了薄膜形成的表面自由能(分离压力)的分量。对于曲面,解离力应与拉普拉斯毛细压力相结合,以给出开尔文方程的正确形式。Bangham和Deryaguin的早期工作表明,薄的液体层具有异常的物理性质。讨论了这些研究与液膜厚度的关系。第二部分给出了低能表面上液体薄膜临界破裂厚度的新实验证据。一些纯液体在低能量表面上自发破裂,如蜡或聚四氟乙烯,厚度非常大(0.01厘米)。含水盐和表面活性剂溶液的作用表明,这些远程力的来源是电。
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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