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Surface Tension and Adsorption Studies by Drop Profile Analysis Tensiometry

机译:通过液滴轮廓分析张力法研究表面张力和吸附

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摘要

Surface tension and dilational viscoelasticity of solutions of various surfactants measured with bubble and drop profile analysis tensiometry are discussed. The study also includes experiments on the co-adsorption of surfactant molecules from a solution drop and alkane molecules from saturated alkane vapor phase. Using experimental data for 12 surfactants with different surface activities, it is shown that depletion due to adsorption of surfactant from the drop bulk can be significant. An algorithm is proposed quantitatively to take into consideration the depletion effect which is required for a correct description of the co-adsorption of alkanes on the solution drop surface and the correct analysis of experimental dynamic surface tension data to determine the adsorption mechanism. Bubble and drop profile analysis tensiometry is also the method of choice for measuring the dilational viscoelasticity of the adsorbed interfacial layer. The same elasticity moduli are obtained with the bubble and drop method only when the equilibrium surface pressures are sufficiently small (Π < 15 mN m−1). When the surface pressure for a surfactant solution is larger than this value, the viscoelasticity moduli determined from drop profile experiments become significantly larger than those obtained from bubble profile measurements.
机译:讨论了用气泡和液滴轮廓分析张力法测量的各种表面活性剂溶液的表面张力和膨胀粘弹性。该研究还包括对溶液液滴中表面活性剂分子与饱和烷烃气相中烷烃分子的共吸附实验。使用具有不同表面活性的12种表面活性剂的实验数据表明,由于从滴剂主体中吸附了表面活性剂而导致的损耗可能很大。定量提出了一种算法,考虑了正确描述烷烃在液滴表面上的共吸附所需的耗竭效应以及对实验动态表面张力数据的正确分析以确定吸附机理所需的耗竭效应。气泡和液滴轮廓分析张力法也是测量吸附的界面层的膨胀粘弹性的选择方法。仅当平衡表面压力足够小(Π<15 mN m -1 )时,才能通过气泡和滴落法获得相同的弹性模量。当表面活性剂溶液的表面压力大于该值时,由液滴分布实验确定的粘弹性模量明显大于从气泡分布测量获得的粘弹性模量。

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