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Hydrodynamics of dip-coated thin films in the presence of evaporation, and, Surfactant structures controlling spontaneous dewetting.

机译:在存在蒸发的情况下浸涂薄膜的流体动力学,以及控制自发去湿的表面活性剂结构。

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摘要

In this dissertation, we discuss the investigation of two problems in dynamic wetting: the hydrodynamics of dip-coated, finite-length films of evaporative fluids and the surfactant structures controlling the spontaneous dewetting of a surfactant solution.; While films pulled from non-volatile fluids on a vertical substrate are essentially infinite in length, films pulled from volatile fluids have a finite length. We examine such finite films using three well-controlled oligomer liquids as well as surfactant solutions. We find that the finite length of the film is controlled by a global balance between mass lost by evaporation and mass input by viscous forces. While the attendant thermally driven Marangoni flows have small impact on the mass balance, they do alter the velocity field in the film in the direction parallel to the substrate. Using measured film profiles, wit have developed a novel method to determine the combined effects of evaporation and Marangoni flow on velocity and pressure fields in the film. This method is independent of any specific model of the evaporation process. In preliminary studies with surfactant solutions, we observed strong effects of solutal Marangoni flows on dip-coated films.; For the second problem, we examine the structures of self-assemblies left on a solid as a contact line spontaneously retreats across a surface during an autophobing event. We find that surfactants of a continuous structural gradient are deposited: from molecules lying down on the surface with low packing densities in a region never touched by the solution, to molecules standing up with higher packing densities in a region where the contact line has moved slowly. Despite significant free volumes within the self-assemblies, we see no evidence of clustering of molecules. We see a clear correlation between contact line speed and the surfactant structures. We show that the dynamics during at least a later period of the autophobing event is dominated by the time evolution of Young's force dictated by the self-assembly near the contact line.
机译:在本文中,我们讨论了动态润湿中的两个问题的研究:蒸发流体的有限长度浸涂的流体动力学和控制表面活性剂溶液自发润湿的表面活性剂结构。虽然从垂直基底上的非挥发性流体拉出的膜的长度基本上是无限的,但是从挥发性流体中拉出的膜的长度是有限的。我们使用三种控制良好的低聚物液体以及表面活性剂溶液检查了这种有限的膜。我们发现,薄膜的有限长度受蒸发损失的质量与粘性力输入的质量之间的全局平衡控制。虽然伴随着热驱动的马兰戈尼流对质量平衡的影响很小,但它们确实会在平行于基材的方向上改变膜中的速度场。通过测量膜的轮廓,机智开发了一种新颖的方法来确定蒸发和马兰戈尼流对膜中速度和压力场的综合影响。该方法与蒸发过程的任何特定模型无关。在表面活性剂溶液的初步研究中,我们观察到了Marangoni溶液对浸涂膜的强烈影响。对于第二个问题,我们检查了自线事件期间接触线自发地在表面上后退时,留在固体上的自组装结构。我们发现沉积了连续结构梯度的表面活性剂:从在溶液从未接触过的区域中堆积密度低的表面上的分子,到接触线缓慢移动的区域中堆积密度高的分子, 。尽管自组装体内有大量自由体积,但我们看不到分子聚集的迹象。我们看到接触线速度和表面活性剂结构之间有明显的相关性。我们表明,至少在自拍事件的后期,动力学是由接触线附近的自组装所决定的杨氏力的时间演化决定的。

著录项

  • 作者

    Qu, Dan.;

  • 作者单位

    Carnegie Mellon University.;

  • 授予单位 Carnegie Mellon University.;
  • 学科 Physics Condensed Matter.; Physics Fluid and Plasma.; Engineering Materials Science.
  • 学位 Ph.D.
  • 年度 2001
  • 页码 137 p.
  • 总页数 137
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 等离子体物理学;工程材料学;
  • 关键词

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