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各向同性相球形非离子表面活性剂胶束的结构、热力学和动力学。

Structure, thermodynamics and dynamics of the isotropic phase of spherical non-ionic surfactant micelles.

机构信息

Université de Lyon, Laboratoire de Physique, École Normale Supérieure de Lyon, CNRS-UMR 5672, 46 allée d'Italie, 69364 Lyon, France.

出版信息

J Colloid Interface Sci. 2013 Mar 1;393:161-73. doi: 10.1016/j.jcis.2012.10.039. Epub 2012 Nov 8.

DOI:10.1016/j.jcis.2012.10.039
PMID:23201065
Abstract

We investigate a non-ionic surfactant (C(12)E(8))/water binary mixture, over a wide range of concentrations and temperatures (i.e. 1-35 wt.% of C(12)E(8) and 10-60 °C in temperature) by means of different experimental techniques: Small-Angle Neutron Scattering (SANS), Quasi Elastic Light Scattering (QELS) and High Frequency Rheology. The aims of this work are to provide information on structure, thermodynamics and dynamics of the isotropic phase of such a micellar system and, by combining these different types of information, to obtain a comprehensive image of the behaviour of this phase. Our results demonstrate that structural, thermodynamic and dynamic properties of these solutions are fully monitored by the temperature-induced changes in the ethylene-glycol chain hydration. They confirm that C(12)E(8) micelles are spherical and do not grow in the investigated range of concentrations and temperatures. They demonstrate that the interaction potential between C(12)E(8) micelles is more complicated than what was previously described, with an additional repulsive interaction. They allow us to put forward explanations for the Isotropic-Ordered phase transition as well as for the temperature behaviour of the viscosity of C(12)E(8) micellar solutions. Our investigation provides new and valuable information on the dynamics of these mixtures that reflect the complexity of the interaction potential between the C(12)E(8) micelles. It shows that concentrated solutions exhibit a viscoelastic behaviour that can be described by a simple Maxwell model.

摘要

我们通过小角中子散射(SANS)、准弹性光散射(QELS)和高频流变学等不同实验技术,研究了一种非离子表面活性剂(C(12)E(8))/水二元混合物,浓度和温度范围很广(即 C(12)E(8)为 1-35wt.%,温度为 10-60°C)。这项工作的目的是提供关于这种胶束系统各向同性相的结构、热力学和动力学信息,并通过结合这些不同类型的信息,获得该相行为的综合图像。我们的结果表明,这些溶液的结构、热力学和动力学性质完全受温度诱导的乙二醇链水合变化的影响。它们证实 C(12)E(8)胶束是球形的,并且在研究的浓度和温度范围内不会生长。它们表明 C(12)E(8)胶束之间的相互作用势比以前描述的更复杂,存在额外的排斥相互作用。它们使我们能够对各向同性-有序相转变以及 C(12)E(8)胶束溶液的粘度随温度的行为提出解释。我们的研究为这些混合物的动力学提供了新的有价值的信息,反映了 C(12)E(8)胶束之间相互作用势的复杂性。它表明,在浓度较高的溶液中表现出粘弹性行为,可以用简单的麦克斯韦模型来描述。

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