Lopez JM, Hirsa A
Department of Mathematics and Earth System Science Center, The Pennsylvania State University, University Park, Pennsylvania, 16802
J Colloid Interface Sci. 1998 Oct 1;206(1):231-239. doi: 10.1006/jcis.1998.5720.
Recent developments in nonlinear optical techniques for noninvasive probing of a surfactant influenced gas/liquid interface allow for the measurement of the surfactant surface concentration, c, and thus provide new opportunities for the direct determination of its intrinsic viscosities. Here, we present the theoretical foundations, based on the Boussinesq-Scriven surface model without the usual simplification of constant viscosities, for an experimental technique to directly measure the surface shear (µs) and dilatational (kappas) viscosities of a Newtonian interface as functions of the surfactant surface concentration. This ability to directly measure the surfactant concentration permits the use of a simple surface flow for the measurement of the surface viscosities. The requirements are that the interface must be nearly flat, and the flow steady, axisymmetric, and swirling; these flow conditions can be achieved in the deep-channel viscometer driven at relatively fast rates. The tangential stress balance on such an interface leads to two equations; the balance in the azimuthal direction involves only µs and its gradients, and the balance in the radial direction involves both µs and kappas and their gradients. By further exploiting recent developments in laser-based flow measuring techniques, the surface velocities and their gradients which appear in the two equations can be measured directly. The surface tension gradient, which appears in the radial balance equation, is incorporated from the equation of state for the surfactant system and direct measurements of the surfactant surface concentration distribution. The stress balance equations are then ordinary differential equations in the surface viscosities as functions of radial position, which can be readily integrated. Since c is measured as a function of radial position, we then have a direct measurement of µs and kappas as functions of c. Numerical computations of the Navier-Stokes equations are performed to determine the appropriate conditions to achieve the requisite secondary flow. Copyright 1998 Academic Press.
用于非侵入式探测受表面活性剂影响的气/液界面的非线性光学技术的最新进展,使得能够测量表面活性剂的表面浓度(c),从而为直接测定其特性粘度提供了新的机会。在此,我们基于Boussinesq-Scriven表面模型(不采用通常的恒定粘度简化),给出一种实验技术的理论基础,该技术可直接测量牛顿界面的表面剪切粘度((\mu_s))和拉伸粘度((\kappa)),作为表面活性剂表面浓度的函数。这种直接测量表面活性剂浓度的能力允许使用简单的表面流动来测量表面粘度。要求是界面必须近乎平坦,且流动稳定、轴对称且呈涡旋状;这些流动条件可以在以相对较快速率驱动的深通道粘度计中实现。在这样一个界面上的切向应力平衡导致两个方程;方位角方向的平衡仅涉及(\mu_s)及其梯度,而径向方向的平衡涉及(\mu_s)和(\kappa)及其梯度。通过进一步利用基于激光的流动测量技术的最新进展,可以直接测量出现在这两个方程中的表面速度及其梯度。出现在径向平衡方程中的表面张力梯度,是从表面活性剂体系的状态方程以及表面活性剂表面浓度分布的直接测量中引入的。然后,应力平衡方程是以表面粘度作为径向位置函数的常微分方程,可以很容易地进行积分。由于(c)是作为径向位置的函数进行测量的,所以我们可以直接测量(\mu_s)和(\kappa)作为(c)的函数。对Navier-Stokes方程进行了数值计算,以确定实现所需二次流动的合适条件。版权所有1998年学术出版社。