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Squeezing molecular thin alkane lubrication films between curved solid surfaces with long-range elasticity: Layering transitions and wear

机译:在具有长程弹性的弯曲固体表面之间挤压分子薄烷烃润滑膜:分层过渡和磨损

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摘要

The properties of alkane lubricants confined between two approaching solids are investigated by a model that accounts for the curvature and the elastic properties of the solid surfaces. We consider linear alkane molecules of different chain lengths, C3H8, C4H10, C8H18, C9H20, C10H22, C12H26 and C14H30 confined between smooth gold surfaces. In most cases we observe well defined molecular layers develop in the lubricant film when the width of the film is of the order of a few atomic diameters. An external squeezing-pressure induces discontinuous, thermally activated changes in the number n of lubricant layers. We find that with increasing alkane chain length, the transition from n to n-1 layers occurs at higher pressure, as expected based on the increasing wettability ~or spreading pressure with increasing chain length. Thus, the longer alkanes are better boundary lubricants than the shorter ones, and this should result in less wear. We obtain good correlation between our theoretical results and wear experiments.
机译:通过考虑固体表面曲率和弹性的模型,研究了限制在两种接近的固体之间的烷烃润滑剂的性能。我们考虑了限制在光滑金表面之间的不同链长的线性烷烃分子,C3H8,C4H10,C8H18,C9H20,C10H22,C12H26和C14H30。在大多数情况下,当润滑膜的宽度约为原子直径的数量级时,我们会在润滑膜中观察到清晰定义的分子层。外部挤压压力引起润滑剂层数n的不连续,热激活的变化。我们发现,随着烷烃链长的增加,从n到n-1层的转变在较高的压力下发生,这是基于随着链长的增加而增加的可湿性或扩散压力所预期的。因此,与较短的烷烃相比,较长的烷烃是更好的边界润滑剂,因此应减少磨损。我们在理论结果和磨损实验之间获得了良好的相关性。

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