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Capillary wave theory of adsorbed liquid films and the structure of the liquid-vapor interface

机译:吸附液膜毛细波理论及液 - 蒸汽界面的结构

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In this paper we try to work out in detail the implications of a microscopic theory for capillary waves under the assumption that the density is given along lines normal to the interface. Within this approximation, which may be justified in terms of symmetry arguments, the Fisk-Widom scaling of the density profile holds for frozen realizations of the interface profile. Upon thermal averaging of capillary wave fluctuations, the resulting density profile yields results consistent with renormalization group calculations in the one-loop approximation. The thermal average over capillary waves may be expressed in terms of a modified convolution approximation where normals to the interface are Gaussian distributed. In the absence of an external field we show that the phenomenological density profile applied to the square-gradient free energy functional recovers the capillary wave Hamiltonian exactly. We extend the theory to the case of liquid films adsorbed on a substrate. For systems with short-range forces, we recover an effective interface Hamiltonian with a film height dependent surface tension that stems from the distortion of the liquid-vapor interface by the substrate, in agreement with the Fisher-Jin theory of short-range wetting. In the presence of long-range interactions, the surface tension picks up an explicit dependence on the external field and recovers the wave vector dependent logarithmic contribution observed by Napiorkowski and Dietrich. Using an error function for the intrinsic density profile, we obtain closed expressions for the surface tension and the interface width.We show the external field contribution to the surface tension may be given in terms of the film's disjoining pressure. From literature values of the Hamaker constant, it is found that the fluid-substrate forces may be able to double the surface tension for films in the nanometer range. The film height dependence of the surface tension described here is in full agreement with results of t
机译:在本文中,我们尝试详细阐述微观理论在假设沿垂直线到界面的线路给出的密度的假设下的毛细波的影响。在该近似值中,这可以在对称参数方面是合理的,所以密度分布的FICK - WIDOM缩放保持用于接口简档的冻结的实现。在毛细波波动的热平均时,所得到的密度曲线产生结果与单环近似值中的重整化组计算一致。毛细管波的热平均值可以以修改的卷积近似表示,其中界面的正常是高斯分布的。在没有外部领域的情况下,我们表明应用于方形梯度自由能量功能的现象学密度分布始终恢复毛细管汉菲尔顿人。我们将理论扩展到吸附在基材上的液体膜的情况。对于具有短程力的系统,我们恢复有效接口Hamiltonian,其具有薄膜高度依赖性表面张力,该张力源于基板的液态蒸汽接口的变形,同时与短程润湿性的Fisher-Jin理论一致。在远程相互作用的存在下,表面张力拾取了对外部场的明确依赖性,并恢复了Napiorkowski和饮食中观察到的波矢量依赖性对数贡献。使用误差函数对于固有密度曲线,我们获得表面张力的封闭表达,并且界面宽度.We示出了在薄膜的脱气压力方面给出了对表面张力的外部场贡献。从哈姆拉恒定的文献值,发现流体 - 基板力可以能够将纳米范围内的薄膜的表面张力加倍。这里描述的表面张力的薄膜高度依赖性与t的结果完全一致

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