Areshi Mounirah, Tseluiko Dmitri, Thiele Uwe, Goddard Benjamin D, Archer Andrew J
Department of Mathematical Sciences, Loughborough University, Loughborough LE11 3TU, United Kingdom.
Department of Mathematics, Faculty of Science, University of Tabuk, P. O. Box 741, Tabuk 71491, Saudi Arabia.
Phys Rev E. 2024 Feb;109(2-1):024801. doi: 10.1103/PhysRevE.109.024801.
We present a theory for the interfacial wetting phase behavior of binary liquid mixtures on rigid solid substrates, applicable to both miscible and immiscible mixtures. In particular, we calculate the binding potential as a function of the adsorptions, i.e., the excess amounts of each of the two liquids at the substrate. The binding potential fully describes the corresponding interfacial thermodynamics. Our approach is based on classical density functional theory. Binary liquid mixtures can exhibit complex bulk phase behavior, including both liquid-liquid and vapor-liquid phase separation, depending on the nature of the interactions among all the particles of the two different liquids, the temperature, and the chemical potentials. Here we show that the interplay between the bulk phase behavior of the mixture and the properties of the interactions with the substrate gives rise to a wide variety of interfacial phase behaviors, including mixing and demixing situations. We find situations where the final state is a coexistence of up to three different phases. We determine how the liquid density profiles close to the substrate change as the interaction parameters are varied and how these determine the form of the binding potential, which in certain cases can be a multivalued function of the adsorptions. We also present profiles for sessile droplets of both miscible and immiscible binary liquids.
我们提出了一种适用于刚性固体基底上二元液体混合物界面润湿相行为的理论,该理论适用于可混溶和不可混溶的混合物。具体而言,我们计算了作为吸附量函数的结合势,即基底上两种液体各自的过量量。结合势完全描述了相应的界面热力学。我们的方法基于经典密度泛函理论。二元液体混合物可表现出复杂的体相行为,包括液 - 液相分离和气 - 液相分离,这取决于两种不同液体所有粒子间相互作用的性质、温度和化学势。在此我们表明,混合物的体相行为与和基底相互作用性质之间的相互作用会产生多种界面相行为,包括混合和分离情况。我们发现存在最终状态为多达三种不同相共存的情况。我们确定了随着相互作用参数变化,靠近基底的液体密度分布如何改变,以及这些如何决定结合势的形式,在某些情况下结合势可能是吸附量的多值函数。我们还给出了可混溶和不可混溶二元液体的固着液滴的分布情况。