Voué M, Rioboo R, Adao M H, Conti J, Bondar A I, Ivanov D A, Blake T D, De Coninck J
Centre de Recherches en Modélisation Moléculaire, Université de Mons-Hainaut/Materia Nova, Parc Initialis, Av. Copernic, 1, B-7000 Mons, Belgium.
Langmuir. 2007 Apr 24;23(9):4695-9. doi: 10.1021/la062884r. Epub 2007 Mar 28.
The static and dynamic wetting properties of self-assembled alkanethiol monolayers of increasing chain length were studied. The molecular-kinetic theory of wetting was used to interpret the dynamic contact angle data and evaluate the contact-line friction on the microscopic scale. Although the surfaces had a similar static wettability, the coefficient of contact-line friction zeta0 increased linearly with alkyl chain length. This result supports the hypothesis of energy dissipation due to a local deformation of the nanometer-thick layer at the contact line.
研究了链长不断增加的自组装烷硫醇单分子层的静态和动态润湿性。采用润湿的分子动力学理论来解释动态接触角数据,并在微观尺度上评估接触线摩擦力。尽管这些表面具有相似的静态润湿性,但接触线摩擦系数ζ0随烷基链长线性增加。这一结果支持了由于接触线处纳米厚层的局部变形导致能量耗散的假设。