Theory of capillary-induced interactions beyond the superposition approximation

被引:24
作者
Dominguez, Alvaro
Oettel, Martin
Dietrich, S.
机构
[1] Univ Seville, Fis Teor, E-41080 Seville, Spain
[2] Johannes Gutenberg Univ Mainz, Inst Phys, D-55099 Mainz, Germany
[3] Max Planck Inst Met Res, D-70569 Stuttgart, Germany
[4] Univ Stuttgart, Inst Theoret & Angew Phys, D-70569 Stuttgart, Germany
关键词
D O I
10.1063/1.2781420
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 [物理化学]; 081704 [应用化学];
摘要
Within a general theoretical framework, we study the effective, deformation-induced interaction between two colloidal particles trapped at a fluid interface in the regime of small deformations. In many studies, this interaction has been computed with the ansatz that the actual interface configuration for the pair is given by the linear superposition of the interface deformations around the single particles. Here, we assess the validity of this approach and compute the leading term of the effective interaction for a large interparticle separation beyond this so-called superposition approximation. As an application, we consider the experimentally relevant case of interface deformations owing to the electrostatic field emanating from charged colloidal particles. In mechanical isolation, i.e., if the net force acting on the total system consisting of the particles plus the interface vanishes, the superposition approximation is actually invalid. The effective capillary interaction is governed by contributions beyond this approximation and turns out to be attractive. For sufficiently small surface charges on the colloids, such that linearization is strictly valid, and at asymptotically large separations, the effective interaction does not overcome the direct electrostatic repulsion between the colloidal particles. (c) 2007 American Institute of Physics.
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页数:17
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