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Nanotribological properties of elastic thin films.

机译:弹性薄膜的纳米摩擦学特性。

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摘要

A considerable number of fundamental and applied studies have focused on the nano-tribological properties of confined, molecularly thin films. Despite these efforts, the molecular-level mechanisms of friction and the corresponding functions of actual lubricant additives and surfactants at solid surfaces are only partially understood. To address some of these issues, thiol self-assembled monolayers (SAMs) were studied in single-asperity contacts, as model systems for the natural boundary lubrication of solid surfaces by the aromatics content in mineral oil-based fuels and lubricants. Friction force microscopy, a technique based on atomic force microscopy (AFM), and the Surface Forces Apparatus (SFA) were used to investigate the effects of molecular packing, adhesion strength, and sliding speed on the friction of self-assembled monolayers of the aromatic compounds thiophenol, p-phenylthiophenol, p-terphenylthiol, 2-naphthalene-thiol, benzyl mercaptan, and phenyl-terminated alkanethiols Ph(CH2)nSH (n = 13-16) on template-stripped gold or silver surfaces. The adhesion between a monolayer-covered tip and substrate was controlled by immersing the sliding contacts in ethanol or in dry N2 gas.;At low loads L, low adhesion (obtained in ethanol) resulted in a linear dependence of the friction force F on load, F = muL, whereas in N2, the higher adhesion between the same monolayers gave a non-linear, apparently area-dependent friction. This nonlinear friction in the adhesive systems was well described by F = ScA, with the contact area, A, calculated for a thin, linearly elastic film confined between rigid substrates using the extended Thin-Coating Contact Mechanics (TCCM) model, and S c being the critical shear stress, a constant for each monolayer system. A systematic change was found in the friction coefficient, mu, obtained in ethanol and the critical shear stress, Sc, obtained in N2 with increasing molecular packing for the aromatic thiols, and with the odd or even number of methylene units for the phenyl-terminated alkanethiols. The investigations have also been extended to preliminary experiments on thin films of polyolefins with and without stretching-induced orientation to study the dependence of friction on the polymer chain orientation.
机译:大量的基础研究和应用研究都集中在受限的分子薄膜的纳米摩擦学特性上。尽管做出了这些努力,但是仅部分地了解了在固体表面上摩擦的分子水平机理以及实际的润滑剂添加剂和表面活性剂的相应功能。为了解决这些问题中的一些,在单粗糙接触中研究了硫醇自组装单分子膜(SAMs),作为通过矿物油基燃料和润滑剂中的芳烃含量对固体表面进行自然边界润滑的模型系统。摩擦力显微镜(一种基于原子力显微镜(AFM)的技术)和表面力仪器(SFA)用于研究分子堆积,粘合强度和滑动速度对芳族化合物自组装单层摩擦的影响在模板剥离的金或银表面上,将苯硫酚,对苯硫酚,对叔苯硫醇,2-萘硫醇,苄硫醇和苯基末端的链烷硫醇Ph(CH2)nSH(n = 13-16)合成化合物。通过将滑动触点浸入乙醇或干燥的N2气体中,可以控制单层覆盖的尖端与基材之间的粘附力;在低载荷L下,低粘附力(在乙醇中获得)导致摩擦力F与载荷呈线性关系,F =μL,而在N 2中,相同单层之间的较高粘附力产生非线性的,显然是面积依赖性的摩擦。 F = ScA很好地描述了粘合剂系统中的这种非线性摩擦,其中接触面积A是使用扩展的薄涂层接触力学(TCCM)模型计算的,限制在刚性基材之间的线性弹性薄膜的厚度,而S c是临界剪切应力,每个单层系统的常数。发现系统中的变化是:在乙醇中获得的摩擦系数μu和在N2中获得的临界剪切应力Sc随芳香族硫醇分子堆积的增加以及苯基端基的亚甲基单元的奇数或偶数而变化。链烷硫醇。研究也已扩展到对有或没有拉伸诱导取向的聚烯烃薄膜的初步实验,以研究摩擦对聚合物链取向的依赖性。

著录项

  • 作者

    Yang, Yutao.;

  • 作者单位

    University of Massachusetts Lowell.;

  • 授予单位 University of Massachusetts Lowell.;
  • 学科 Chemistry Molecular.;Engineering Materials Science.;Chemistry Physical.
  • 学位 Ph.D.
  • 年度 2010
  • 页码 156 p.
  • 总页数 156
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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