Wu Jiyu, Farouk T, Ward C A
Thermodynamics and Kinetics Laboratory, Department of Mechanical and Industrial Engineering, University of Toronto, Toronto, Canada M5S 3G8.
J Phys Chem B. 2007 Jun 7;111(22):6189-97. doi: 10.1021/jp071372y. Epub 2007 May 12.
When a liquid and its vapor contact a smooth, homogeneous surface, Gibbsian thermodynamics indicates that the contact angle depends on the pressure at the three-phase line of an isothermal system. When a recently proposed adsorption isotherm for a solid-vapor interface is combined with the equilibrium conditions and the system is assumed to be in a cylinder where the liquid-vapor interface can be approximated as spherical, the contact-angle-pressure relation can be made explicit. It indicates that a range of contact angles can be observed on a smooth homogeneous surface by changing the pressure at the three-phase line, but it also indicates that the adsorption at the solid-liquid interface is negative, and leads to the prediction that the contact angle increases with pressure. The predicted dependence of the contact angle on pressure is investigated experimentally in a system that has an independent mechanism for determining when thermodynamic equilibrium is reached. The predictions are in agreement with the measurements. The results provide a possible explanation for contact angle hysteresis.
当液体及其蒸汽接触光滑、均匀的表面时,吉布斯热力学表明接触角取决于等温系统三相线处的压力。当最近提出的固 - 汽界面吸附等温线与平衡条件相结合,且系统被假定处于一个圆柱形容器中,其中液 - 汽界面可近似为球形时,接触角与压力的关系就可以明确得出。这表明通过改变三相线处的压力,可以在光滑均匀的表面上观察到一系列接触角,但这也表明固 - 液界面处的吸附是负的,并导致预测接触角随压力增加。在一个具有独立机制来确定何时达到热力学平衡的系统中,对预测的接触角与压力的依赖关系进行了实验研究。预测结果与测量结果一致。这些结果为接触角滞后现象提供了一种可能的解释。