Dynamic wetting: Hydrodynamic or molecular-kinetic?

被引:94
作者
Ranabothu, SR [1 ]
Karnezis, C [1 ]
Dai, LL [1 ]
机构
[1] Texas Tech Univ, Dept Chem Engn, Lubbock, TX 79409 USA
关键词
contact angles; dynamic wetting; hydrodynamic model; molecular-kinetic model; combined model; contact angle hysteresis;
D O I
10.1016/j.jcis.2005.02.074
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 [物理化学]; 081704 [应用化学];
摘要
The dynamic wetting behavior of simple liquids (water, glycerin, formamide, ethylene glycol, and a mixture of water and ethylene glycol) and polydimethylsiloxane (PDMS) oils with different viscosities has been investigated. The hydrodynamic, molecular-kinetic, and combined molecular-hydrodynarnic models have been applied to the experimental results to evaluate the models' adequacy. Our work suggests that the molecular displacement, i.e., the adsorption and desorption process, seems to be dominant for the simple liquids investigated. For polydimethylsiloxanes, Our work suggests that none of the evaluated models is sufficient to explain the experimentally observed dependence of the dynamic contact angle on contact velocity. This work, to the best of our knowledge, provides the first extensive comparison of the three models with experimental data over a wide range of viscosity. In addition, we have investigated the contact angle hysteresis and conclude that it is a strong function of the contact speed, the interactions between the fluids and the substrate, and the fluid viscosity. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:213 / 221
页数:9
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