Boundary viscosity of polydimethylsiloxane liquids and their binary mixtures

B. V. Deryaguin, V. Karasev, I. Lavygin, I. I. Skorokhodov, E. N. Khromova
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引用次数: 21

Abstract

A systematic study is made of the boundary viscosity of a number of polydimethylsiloxane liquids (PMS) of molecular weights ranging from 1,000 to 40,000 by the blow-off method, film thicknesses being measured by a modulation-polarimetric (elliposmetric) precedure. It is established experimentally that the viscosity of the liquids studied is not the same throughout the thickness of the boundary later.PMS applied to glass and steel substrates retain their bulk viscosity values down to a layer thickness of ca. 150–200 A, below which the viscosity increases slightly. On further decrease of the distance to 10–15 A from the substrate, the viscosity becomes anomalously low, amounting to about 10–20 % of the bulk value. The existence of a layer of anomalously low viscosity may be attributed to orientation of the PMS molecules in the plane of the substrate, and hence, to the ease with which these oriented layers slip relative to one another.When studying the boundary viscosity of binary mixtures of PMS of different molecular weights, boundary phases of elevated viscosity were found to exist at a distance of 15–30 A from the substrate. This phenomenon may be attributed to a change in concentration of the mixture at the solid surface i.e., to an increase in content of the component with the higher molecular weight in the wall-adjacent layer.
聚二甲基硅氧烷液体及其二元混合物的边界粘度
用吹脱法对分子量为1000 ~ 40000的聚二甲基硅氧烷液体(PMS)的边界粘度进行了系统的研究,并用调制偏振法(椭圆法)测量了膜厚。实验证明,所研究液体的黏度在整个边界厚度上是不相同的。应用于玻璃和钢基板的PMS在约150-200 a的层厚下保持其体积粘度值,低于此粘度略有增加。当距离基材进一步减小到10-15 A时,粘度变得异常低,约为体积值的10 - 20%。异常低粘度层的存在可能归因于PMS分子在衬底平面上的取向,因此,这些取向层相对于彼此滑动的容易程度。在研究不同分子量PMS二元混合物的边界粘度时,发现黏度较高的边界相存在于距离底物15-30 a处。这种现象可归因于固体表面混合物浓度的变化,即临近壁层中分子量较高的组分含量的增加。
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