首页> 外文期刊>RSC Advances >Moving mechanisms of the three-phase contact line in a water–decane–silica system
【24h】

Moving mechanisms of the three-phase contact line in a water–decane–silica system

机译:水-癸烷-二氧化硅系统中三相接触线的移动机理

获取原文
           

摘要

The movement of the three-phase contact line with chain molecules in the liquid phase displays more complex mechanisms compared to those in the usual liquid–liquid–solid systems and even to the gas–liquid–solid systems controlled by the traditional single-molecule adsorption–desorption mechanisms. By introducing decane molecules with chain structures, we demonstrate from molecular dynamics insights that the moving mechanism of the contact line in a water–decane–silica system is totally different from traditional mechanisms. Three different wettability-related moving mechanisms including “Roll up”, “Piston” and “Shear” are revealed corresponding to the hydrophilic, intermediate and hydrophobic three-phase wettability, respectively. In the “Roll up” mechanism, the decane molecules are rolled up by the competitively adsorbed water molecules and then move forward under the driving force; when the “Piston” mechanism happens, the decane molecules are pushed by the piston-like water phase owing to the comparable adsorption interactions of the two liquids on the solid surface; in the “Shear” mechanism, the contact line is hard to drive due to the stronger decane–silica interactions but the decane molecules far away from the solid surface will move forward. Besides, the time-averaged velocity of the moving contact line is greatly related to the moving mechanisms. For the “Roll up” mechanism, the contact line velocity increases first and then reaches a steady value; for the “Piston” mechanism, the contact line velocity has a maximum value at the start-up stage and then decreases to a stable value; for the “Shear” mechanism, the contact line velocity fluctuates around zero due to the thermal fluctuation of the molecules. Additionally, the mean distance from Molecular Kinetics Theory increases with decreasing hydrophilicity and the displacement frequency in “Roll up” mechanism is 2 orders of magnitude higher than that in the “Piston” mechanism, further demonstrating the different moving mechanisms from a quantitative point of view.
机译:与通常的液-液-固系统,甚至是传统的单分子吸附控制的气-液-固系统相比,液相中具有链分子的三相接触线的运动显示出更复杂的机理-解吸机制。通过引入具有链结构的癸烷分子,我们从分子动力学的角度证明了水-癸烷-二氧化硅系统中接触线的移动机理与传统机理完全不同。揭示了三种不同的与润湿性有关的移动机理,分别是“卷起”,“活塞”和“剪切”,分别对应于亲水,中间和疏水的三相润湿性。在“卷起”机制中,癸烷分子被竞争性吸附的水分子卷起,然后在驱动力的作用下向前移动。当发生“活塞”机理时,由于两种液体在固体表面的可比吸附相互作用,癸烷分子被活塞状水相推动。在“剪切”机制中,由于癸烷与二氧化硅之间的相互作用更强,因此难以驱动接触线,但远离固体表面的癸烷分子将向前移动。此外,动触线的时间平均速度与动机构有很大关系。对于“卷起”机制,接触线速度首先增加,然后达到稳定值。对于“活塞”机构,接触线速度在启动阶段具有最大值,然后降低到稳定值;对于“剪切”机制,由于分子的热波动,接触线速度在零附近波动。此外,与分子动力学理论的平均距离随着亲水性的降低而增加,“向上滚动”机理中的位移频率比“活塞”机理中的位移频率高2个数量级,从定量的角度进一步证明了不同的运动机理。 。

著录项

获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号