Chemical influences on the use of kinetic or equilibrium approaches in reactive wetting

被引:7
作者
Mo, GCH [1 ]
Kwok, DY [1 ]
机构
[1] Univ Alberta, Dept Mech Engn, Nanoscale Technol & Engn Lab, Edmonton, AB T6G 2G8, Canada
关键词
reactive wetting; capillarity; Laplace equation; adsorption kinetics; self-assembled monolayers;
D O I
10.1016/j.colsurfa.2003.07.008
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 ; 081704 ;
摘要
Recent work by Lee et al. [Phys. Rev. E, 65 (2002) 051602] on self-propulsion of liquid via adsorption showed that droplet length has an adverse effect on droplet velocity in reactive wetting experiments. A similar study by Dos Santos and Ondarcuhu [Phys. Rev. Lett, 75 (1995) 2972], however, correlated a positive effect of length-to-velocity. We present an analysis of the forces involved and examine whether kinetic or equilibrium approaches should be used for reactive wetting systems. We found that suitable treatment for droplet adsorption progress can be inferred from the relative length of the droplet. Increased adsorption reaction and the increased drag force associated with a longer droplet compete with each other, resulting in an overall length effect on droplet velocity. We also propose the existence of a transition zone in the overall relationship which consider the contributions from both of the two reaction regimes. By comparison with experimental data, we also found that capillary length of the carrier liquid could be a good indication to where this transition is likely to occur. (C) 2003 Elsevier B.V. All rights reserved.
引用
收藏
页码:169 / 174
页数:6
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