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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Coalescence and Noncoalescence of Sessile Drops: Impact of Surface Forces
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Coalescence and Noncoalescence of Sessile Drops: Impact of Surface Forces

机译:无滴的聚结和非聚结:表面力的影响

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Due to capillarity, sessile droplets of identical liquids will instantaneously fuse when they come in contact at their three-phase lines. However, with drops of different, completely miscible liquids, instantaneous coalescence can be suppressed. Instead, the drops remain in a state of noncoalescence for some time, with the two drop bodies connected only by a thin neck. The reason for this noncoalescence is the surface tension difference, Δγ, between the liquids. If Δγ is sufficiently large, then it induces a sufficiently strong Marangoni flow, which keeps the main drop bodies temporarily separated. Studies with spreading drops have revealed that the boundary between instantaneous coalescence and noncoalescence is sharp (Karpitschka, S.; Riegler, H. J. Fluid. Mech. 2014, 743, R1). The boundary is a function of two parameters only: Δγ and Θ_a, the arithmetic mean of the contact angles in the moment of drop?drop contact. It appears plausible that surface forces (the disjoining pressure) could also influence the coalescence behavior. However, in experiments with spreading drops, surface forces always promote coalescence and their influence might be obscured. Therefore, we present here coalescence experiments with partially wetting liquids and compare the results to the spreading case. We adjust different equilibrium contact angles (i.e., different surface forces) with different substrate surface coatings. As for spreading drops, we observe a sharp boundary between regimes of coalescence and noncoalescence. The boundary follows the same power law relation for both partially and completely wetting cases. Therefore, we conclude that surface forces have no significant, explicit influence on the coalescence behavior of sessile drops from different miscible liquids.
机译:由于毛细管现象,当相同液体的无固定液滴在其三相线处接触时会瞬间融合。但是,使用不同的,完全可混溶的液滴,可以抑制瞬时聚结。相反,液滴保持非凝结状态一段时间,两个液滴仅通过细颈连接。这种不凝结的原因是液体之间的表面张力差Δγ。如果Δγ足够大,则它会引起足够强的Marangoni流动,从而使主要液滴体暂时分离。对液滴扩散的研究表明,瞬时聚结和非聚结之间的边界很明显(Karpitschka,S .; Riegler,H.J. Fluid。Mech。2014,743,R1)。边界仅是两个参数的函数:Δγ和Θ_a,即滴落接触瞬间接触角的算术平均值。表面力(分离压力)也可能影响聚结行为似乎是合理的。但是,在具有分散液滴的实验中,表面力始终会促进聚结,并且其影响可能会被掩盖。因此,我们在此介绍部分润湿液体的聚结实验,并将结果与​​扩散情况进行比较。我们针对不同的基材表面涂层调整不同的平衡接触角(即不同的表面力)。至于散布液滴,我们观察到聚结和非聚结机制之间存在清晰的边界。对于部分和完全润湿的情况,边界都遵循相同的幂定律关系。因此,我们得出结论,表面力对来自不同可混溶液体的无滴液滴的聚结行为没有显着,明确的影响。

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