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Confinement-Induced Symmetry Breaking of Interfacial Surfactant Layers

机译:界面活性剂层的局限性对称破坏

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摘要

Interaction forces between mesoscopic objects are fundamental to soft-condensed matter and are among the prime targets of investigation in colloidal systems.Surfactant molecules are often used to tailor these interactions.The forces are experimentally accessible and for a first theoretical analysis one can make use of a parallel-plate geometry.We present molecularly realistic self-consistent field calculations for an aqueous nonionic surfactant solution near the critical micellization concentration,in contact with two hydrophobic surfaces.The surfactants adsorb cooperatively,and form a monolayer onto each surface.At weak overlap the force increases with increasing compression of the monolayers until suddenly a symmetry braking takes place.One of the monolayers is removed jump-like and as the remaining monolayer can relax,some attraction is observed,which gives way to repulsion at further confinement.The restoring of symmetry at strong confinement occurs as a second-order transition and the force jumps once again from repulsion to attraction.It is anticipated that the metastable branch of the interaction curve will be probed in a typical force experiment.Under normal conditions pronounced hysteresis in the surface force is predicted,without the need to change the adsorbed amount jump-like.
机译:介观物体之间的相互作用力是软凝结物质的基础,是胶体系统研究的主要目标之一。表面活性剂分子通常用于定制这些相互作用。我们提出了在临界胶束化浓度附近,与两个疏水表面接触的非离子表面活性剂水溶液的分子现实的自洽场计算,该表面活性剂协同吸附并在每个表面上形成单层。力随着单层压缩的增加而增加,直到突然发生对称制动为止。其中一个单层被跳跃状移除,并且由于剩余的单层可以松弛,因此观察到了一些吸引力,从而在进一步限制时被排斥。在强约束下的对称性发生为二阶跃迁,力再次从排斥力跃迁到吸引力。预计在典型的力实验中将探测相互作用曲线的亚稳态分支。在正常条件下,可以预测表面力有明显的滞后现象,而无需改变吸附量跳跃般。

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