论文标题
溶质引起的自螺旋液滴的抖动运动
Solute Induced Jittery Motion of Self-Propelled Droplets
论文作者
论文摘要
研究了溶质在自我销售液滴活性中的重要作用。在考虑表面活性剂的四甲基三甲基铵(TTAB)水溶液中,自生产微米大小的4-戊基-4-二苯基碳硝基(5CB)液滴系统。结果表明,添加甘油会导致活性5CB液滴表现出从光滑到抖动运动的过渡。该运动被发现独立于液滴尺寸和5CB的列态。用聚丙烯酰胺(PAAM),聚乙烯基吡咯烷酮(PVP)和聚乙烯醇(PVA)进行类似实验,因为溶质证实,这种过渡不能仅仅基于系统的粘度或Peclet数量来解释。我们提出,溶质和液滴界面之间物理化学相互作用的特定性质是该过渡的根源。实验表明,在溶质存在下,界面处与表面活性剂的流入和重新分布相关的时间量表会改变。甘油和PVP显着提高了5CB液滴的溶解速率,从而使吸附的TTAB分子在界面上更快地重新分布,从而导致液滴暂时停止,然后沿独立的方向重新启动。另一方面,在存在PAAM和PVA的情况下,低溶解速率导致平滑轨迹。在存在和不存在溶质的情况下,液滴大小和界面速度测量的时间演变支持了我们的假设。总体而言,我们的结果为由于存在溶质而出现的复杂相互作用提供了基本的见解。
The intriguing role of the presence of solutes in the activity of a self-propelling droplet is investigated. A system of self-propelling micron sized 4-pentyl-4-biphenylcarbonitrile (5CB) droplets in an aqueous solution of tetradecyltrimethylammonium bromide (TTAB) as surfactant is considered. It is shown that addition of glycerol causes the active 5CB droplet to exhibit a transition from smooth to jittery motion. The motion is found to be independent of the droplet size and the nematic state of 5CB. Analogous experiments with Polyacrylamide (PAAm), Polyvinylpyrrolidone (PVP) and Polyvinyl Alcohol (PVA), as solutes confirm that such a transition cannot merely be explained solely based on the viscosity or Peclet number of the system. We propose that the specific nature of physicochemical interactions between the solute and the droplet interface is at the root of this transition. The experiments show that the time-scales associated with the influx and redistribution of surfactants at the interface are altered in the presence of solutes. Glycerol and PVP significantly enhance the rate of solubilization of the 5CB droplets resulting in a quicker re-distribution of the adsorbed TTAB molecules on the interface, causing the droplet to momentarily stop and then restart in an independent direction. On the other hand, low solubilization rates in the presence of PAAm and PVA lead to smooth trajectories. Our hypothesis is supported by the time evolution of droplet size and interfacial velocity measurements in the presence and absence of solute. Overall, our results provide fundamental insights into the complex interactions emerging due to the presence of solutes.