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首页> 外文期刊>Langmuir: The ACS Journal of Surfaces and Colloids >Evaporation of Sessile Droplets of Dilute Aqueous Solutions Containing Sodium n-Alkylates from Polymer Surfaces: Influences of Alkyl Length and Concentration of Solute
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Evaporation of Sessile Droplets of Dilute Aqueous Solutions Containing Sodium n-Alkylates from Polymer Surfaces: Influences of Alkyl Length and Concentration of Solute

机译:从聚合物表面蒸发含正烷基钠的稀水溶液中的无滴液滴:烷基长度和溶质浓度的影响

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摘要

The evaporation of sessile droplets placed on polymer surfaces was studied by microscopic observation of the changes in shape of aqueous solution droplets in which the alkyl lengths and the initial concentrations of sodium n-alkylates were varied. Although the initial contact angles of the droplets were not significantly different, the evaporation process varied significantly with the alkyl length of the sodium n-alkylate employed. For the sodium dodecanoate (C-12), showing the highest surface activity, the concentration was found to have a significant effect on the evaporation process of the droplets. In the evaporation of water droplets, variations in the three distinct stages were caused by the different concentration of solutes distributed near or at the air/water interface. It is revealed that the concentration of droplet solute near the air/water interface requires not only solvent evaporation but also some affinity of the solute for the interface. The initial C-12 concentration-dependence of the evaporation of C-12 solution droplets is discussed with particular emphasis on the sudden spreading or sudden contraction of the contact area near the end of evaporation. It is suggested that the cluster formation by C-12 molecules at the air/liquid interface during the evaporation causes Marangoni instability in an evaporating droplet, and the clusters are expected to move dynamically, depending on the droplet concentration Of C-12, from the droplet center to the contact line and vice versa, showing Marangoni flow along the air/water interface.
机译:通过显微镜观察水溶液液滴形状的变化来研究放置在聚合物表面上的无蒂液滴的蒸发,其中水溶液的烷基长度和正烷基钠的初始浓度均发生了变化。尽管液滴的初始接触角没有显着差异,但蒸发过程随所用正烷基钠的烷基长度而显着变化。对于显示最高表面活性的十二烷酸钠(C-12),发现浓度对液滴的蒸发过程有重大影响。在水滴的蒸发中,三个不同阶段的变化是由分布在空气/水界面附近或在空气/水界面处的溶质浓度不同引起的。揭示了在空气/水界面附近的液滴溶质的浓度不仅需要溶剂蒸发,还需要溶质对界面的某种亲和力。讨论了C-12溶液液滴蒸发的初始C-12浓度依赖性,并特别着重于蒸发结束时接触区域的突然扩散或突然收缩。建议在蒸发过程中在气/液界面上由C-12分子形成的团簇会引起蒸发的液滴中的马兰戈尼不稳定,并且期望团簇根据C-12的液滴浓度而动态地移动。液滴中心到接触线,反之亦然,显示了Marangoni沿空气/水界面的流动。

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