Tominaga Taiki, Takedomi Naoyuki, Biederman Hynek, Furukawa Hidemitsu, Osada Yoshihito, Gong Jian Ping
Graduate School of Science, Hokkaido University, Sapporo 060-0810, Japan.
Department of Macromolecular Physics, Faculty of Mathematics and Physics, Charles University, V Holesovickach 2, 18000 Prague 8, Czech Republic.
Soft Matter. 2008 Apr 15;4(5):1033-1040. doi: 10.1039/b716465c.
In this paper, the frictional behavior of a neutral hydrogel, polyvinyl alcohol (PVA), on smooth solid substrates with various levels of hydrophobicity have been investigated in water using a strain-controlled parallel-plate rheometer. For the sliding velocity dependence of friction, we detected a distinct friction transition on hydrophobic substrates that are strongly adhesive to the gel, while no clear transition was observed on hydrophilic substrates that are weakly adhesive to the gel. Even on the most hydrophobic substrate, the maximum frictional stress is approximately 1/10-1/5 of the gel's elastic modulus under a large normal strain of 26%. Furthermore, the frictional stress on hydrophobic substrates in the high velocity region, larger than the transition, is much lower than that on hydrophilic ones. We attempted to explain these phenomena with the help of two models: a molecular model based on the thermal fluctuations occurring during adsorption-desorption of polymers and a continuum mechanics model based on elastic dewetting and forced wetting.
在本文中,使用应变控制平行板流变仪,研究了中性水凝胶聚乙烯醇(PVA)在水中不同疏水性光滑固体基质上的摩擦行为。对于摩擦力与滑动速度的关系,我们在与凝胶强粘附的疏水基质上检测到明显的摩擦转变,而在与凝胶弱粘附的亲水基质上未观察到明显转变。即使在最疏水的基质上,在26%的大正应变下,最大摩擦应力约为凝胶弹性模量的1/10 - 1/5。此外,在高于转变速度的高速区域,疏水基质上的摩擦应力远低于亲水基质上的摩擦应力。我们试图借助两个模型来解释这些现象:一个基于聚合物吸附 - 解吸过程中发生的热涨落的分子模型,以及一个基于弹性去湿和强制润湿的连续介质力学模型。