Blake T D, De Coninck J
Research and Development, Kodak Limited, Harrow, Middlesex, UK.
Adv Colloid Interface Sci. 2002 Feb 25;96(1-3):21-36. doi: 10.1016/s0001-8686(01)00073-2.
The molecular-kinetic theory of dynamic wetting has been extended to take specific account of solid-liquid interactions. By equating the work of adhesion with the surface component of the specific activation free energy of wetting, equations have been derived which show the way in which solid-liquid interactions modify both the driving force and the resistance to wetting. For a liquid meniscus advancing across the surface of a solid, these two effects have opposing consequences. Thus, strong interactions increase both the driving force and the resistance, while weak interactions decrease the driving force and the resistance. Because of the form of the relationships, the two effects do not simply cancel out. As a result, the maximum rate at which a liquid can wet a solid may exhibit its own maximum at some intermediate level of interaction. Data taken from both experimental and molecular-dynamics simulations are shown to support these findings, which have significant implications for any process where wetting dynamics are important, such as coating.
动态润湿的分子动力学理论已得到扩展,以具体考虑固液相互作用。通过将粘附功与润湿的比活化自由能的表面成分相等同,已推导出一些方程,这些方程表明了固液相互作用改变驱动力和润湿阻力的方式。对于在固体表面前进的液体弯月面,这两种效应具有相反的结果。因此,强相互作用会增加驱动力和阻力,而弱相互作用会降低驱动力和阻力。由于这些关系的形式,这两种效应不会简单地相互抵消。结果,液体润湿固体的最大速率可能在某种中间相互作用水平时呈现出自身的最大值。来自实验和分子动力学模拟的数据均表明支持这些发现,这对于任何润湿动力学很重要的过程(如涂层)都具有重要意义。