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粗糙聚合物表面疏水性增强。

Enhanced hydrophobicity of rough polymer surfaces.

作者信息

Hirvi Janne T, Pakkanen Tapani A

机构信息

Department of Chemistry, University of Joensuu, P.O. Box 111, FIN-80101, Joensuu, Finland.

出版信息

J Phys Chem B. 2007 Apr 5;111(13):3336-41. doi: 10.1021/jp067399j. Epub 2007 Mar 9.

Abstract

Molecular dynamics simulations were used to study the effect of periodic roughness of PE and PVC polymer surfaces on the hydrophobicity. Pillars of different lateral dimensions and heights were derived from flat crystalline surfaces, and the results of nanoscale simulations on the structured surfaces were compared with theoretical predictions of the Wenzel and Cassie equations. Hydrophobicity increased on all rough surfaces, but the increase was greater on the structured PE surfaces because of the larger water contact angle on the flat PE surface than the corresponding PVC surface. Equally sized pillar structures on the two polymers resulted in different equilibrium wetting geometries. Composite contacts were observed on rough PE surfaces, and the contact angle increased with decreasing contact area between the solid and the liquid. Opposite results were obtained for rough PVC surfaces; the contact angle increased with the solid-liquid contact area, in agreement with Wenzel's equation. However, the composite contact was observed if the energies of the wetted and composite contacts were almost equal. Good agreement was obtained between the simulated contact angles and equilibrium droplet shapes and the theories but there were also some limitations of the nanoscale simulations.

摘要

分子动力学模拟被用于研究聚乙烯(PE)和聚氯乙烯(PVC)聚合物表面的周期性粗糙度对疏水性的影响。从平坦的晶体表面衍生出不同横向尺寸和高度的柱状结构,并将结构化表面的纳米尺度模拟结果与文泽尔方程和卡西方程的理论预测进行比较。所有粗糙表面的疏水性均增加,但结构化PE表面的疏水性增加幅度更大,这是因为平坦PE表面上的水接触角比相应的PVC表面更大。两种聚合物上尺寸相同的柱状结构导致了不同的平衡润湿几何形状。在粗糙的PE表面观察到复合接触,且接触角随着固体与液体之间接触面积的减小而增大。对于粗糙的PVC表面则得到相反的结果;接触角随着固液接触面积的增加而增大,这与文泽尔方程一致。然而,如果润湿接触和复合接触的能量几乎相等,则会观察到复合接触。模拟接触角和平衡液滴形状与理论之间取得了良好的一致性,但纳米尺度模拟也存在一些局限性。

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