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Effects of Packing Density and Chain Length on the Surface Hydrophobicity of Thin Films Composed of Perfluoroalkyl Acrylate Chains: A Molecular Dynamics Study

机译:包装密度和链长对全氟烷基链组成的薄膜表面疏水性的影响:分子动力学研究

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摘要

A good understanding of the surface hydrophobicity of fluorinated materials is useful for their application as coating materials. The present study investigates the surface hydrophobicity of perfluoroalkyl acrylate (PFA) thin films using molecular dynamics simulations. Surface hydrophobicity is characterized by examining the contact angle of a water droplet on PFA surfaces and the cavity formation free energy in the vicinity of the surface. It is found that the calculated microscopic contact angles are in good agreement with the experimental results and partially capture the difference in the hydrophobicity of the surface arising from the variation of packing density and side chain length of PFA. The variations of cavity formation free energy in the vicinity of the surface elucidate that the surface hydrophobicity is mainly governed by the packing density rather than the chain length of PFA. The hydrophobicity generally increases with decreasing the packing density to some extent and then turns to decrease as further reducing the packing density. At higher packing density, the surface hydrophobicity slightly decreases with increasing the chain length, while at the lower packing density, the surface hydrophobicity is increased when chain length of PFA is longer than six carbons. Furthermore, we found that the influence of packing density on the surface hydrophobicity is directly related to the variation of the surface roughness and chain flexibility, that is, the surface hydrophobicity increases with increase in the surface roughness, while the chain flexibility plays a secondary role in the enhancement by affecting the stability of water staying near the interface. The study provides a significant insight into the local hydrophobicity and microscopic structure of the PFA surfaces, which would be useful for the application of surface modification.
机译:良好地理解氟化材料的表面疏水性可用于其作为涂料的应用。本研究研究了使用分子动力学模拟的全氟烷基丙烯酸酯(PFA)薄膜的表面疏水性。表面疏水性的特征在于检查PFA表面上的水滴的接触角以及表面附近的空腔形成自由能。结果发现,计算的微观接触角与实验结果吻合良好,并且部分地捕获从PFA的填充密度和侧链长度的变化产生的表面的疏水性差异。表面疏水性在表面疏水性附近的空腔形成自由能的变化主要由填充密度而不是PFA的链长来控制。疏水性通常随着一定程度的减小,然后转动减小进一步降低填充密度。在较高的填充密度下,随着链条长度的增加,表面疏水性略微降低,而在较低的填充密度下,当PFA的链长比六个碳的链长增加,表面疏水性增加。此外,我们发现,填充密度对表面疏水性的影响与表面粗糙度和链柔性的变化直接相关,即,表面疏水性随着表面粗糙度的增加而增加,而链柔性起起二次作用通过影响界面附近的水的稳定性来增强。该研究提供了对PFA表面的局部疏水性和微观结构的显着洞察,这对于应用表面改性是有用的。

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