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The electrical double layer of micelles in ionic surfactant solutions in the presence of a background electrolyte: 2. Moderately concentrated micellar solutions of sodium dodecyl sulfate

机译:在背景电解质存在的情况下,离子表面活性剂溶液中的胶束双电层:2.十二烷基硫酸钠的中等浓度胶束溶液

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摘要

To continue previous studies [1], a model is developed for calculating electrostatic potentials (1)psi(0) and (1)psi(d) corresponding to the surface of micelle core and the Stern layer, respectively, and the degree (1)beta of binding of counterions in moderately concentrated micellar solutions of ionic surfactants. By the example of sodium dodecyl sulfate micellar solutions, dependences of (1)psi(0) and (1)psi(d) on overall concentration n varying over the range from 0.1 to 0.9 M are determined at different NaCl concentrations in the system. The absolute values of (1)psi(0) and (1)psi(d) potentials are found to grow with a rise in the degree of micellization and a reduction in the average intermicellar distances. This growth is greatly pronounced at a low content of the background electrolyte, whereas, in concentrated NaCl solutions (of approximately 0.1 M), potentials (1)psi(0) and (1)psi(d) remain practically constant. Dependence 1 - (1)beta(n) is monotonically decreasing function.
机译:为了继续进行先前的研究[1],开发了一个模型来计算分别对应于胶束核心和斯特恩层表面的静电势(1)psi(0)和(1)psi(d),以及度数(1 β在中等浓度离子表面活性剂胶束溶液中抗衡离子结合的β。以十二烷基硫酸钠胶束溶液为例,在系统中不同的NaCl浓度下,确定(1)psi(0)和(1)psi(d)对总浓度n的依赖性在0.1到0.9 M之间变化。发现(1)psi(0)和(1)psi(d)电势的绝对值随着胶束化程度的提高和平均胶束间距离的减小而增长。这种增长在低含量的本底电解质中非常明显,而在浓NaCl溶液(约0.1 M)中,电势(1)psi(0)和(1)psi(d)实际上保持恒定。依赖项1-(1)beta(n)是单调递减函数。

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