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Simulations of Nanoindentation of Polymer Surfaces: Effects of Surface Cross-Linking on Adhesion and Hardness

机译:聚合物表面的纳米凸缘模拟:表面交联对粘附性和硬度的影响

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摘要

We present a simulation methodology to chemically cross-link the surface of fully atomistic models of polymers. We simulated nanoindentation of the cross-linked model surfaces whereby nanoparticles (fullerene in this case) are used to probe different regions of the polymer surface enabling us to characterize the surface hardness of the polymer film and calculate the work of adhesion between polymer and nanoparticle. The cross-linked polyester surfaces are constructed using hexamethylene and isophorone di-isocyanate cross-linkers. Our results indicate that, despite surface cross-linking with hexamethylene di-isocyanate molecules, the polymer top surface still maintains significant softness. The hexamethylene cross-links that protrude from the surface are deformable, resulting in a strong adhesion between the surface and carbon particle. In contrast, isophorone surface cross-linking results in significantly weaker adhesion with carbon, due to the less deformable rigid structure formed at the top layer. In this case, while rigidity is imparted to the polymer top surface, the flexibility of the core region of the polymer is maintained.
机译:我们提出了一种化学交联的仿真方法,可以进行聚合物的完全原子模型的表面。我们模拟了交联模型表面的纳米凸缘,由此纳米颗粒(在这种情况下富勒烯)用于探测聚合物表面的不同区域,使我们能够表征聚合物膜的表面硬度并计算聚合物和纳米颗粒之间的粘附工作。交联聚酯表面使用六亚甲基和异佛酮二异氰酸酯交联剂构成。我们的结果表明,尽管表面交联与六亚甲基二异氰酸酯分子交联,但聚合物顶面仍保持显着的柔软性。从表面突出的六亚甲基交联是可变形的,导致表面和碳颗粒之间的强粘附性。相比之下,由于在顶层形成的更易变形的刚性结构,等离子素表面交联导致与碳的粘合显着较弱。在这种情况下,虽然刚度赋予聚合物顶部表面,但保持聚合物的核心区域的柔性。

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