Competitive adsorption of surfactants and hydrophilic silica particles at the oil-water interface: Interfacial tension and contact angle studies

被引:142
作者
Pichot, R. [1 ]
Spyropoulos, F. [1 ]
Norton, I. T. [1 ]
机构
[1] Univ Birmingham, Dept Chem Engn, Ctr Formulat Engn, Birmingham B15 2TT, Edgbaston, England
基金
英国工程与自然科学研究理事会;
关键词
O/W interfacial tension; Contact angle; Silica particles; Surfactant; Interface; Competitive adsorption; COLLOIDAL PARTICLES; FINE PARTICLES; EMULSIONS; STABILIZATION; NANOPARTICLE; MONOGLYCERIDES; TEMPERATURE; WETTABILITY; CAPILLARY; STABILITY;
D O I
10.1016/j.jcis.2012.01.065
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 ; 081704 ;
摘要
The effect of surfactants' type and concentration on the interfacial tension and contact angle in the presence of hydrophilic silica particles was investigated. Silica particles have been shown to have an antagonistic effect on interfacial tension and contact angle in the presence of both W/O and O/W surfactants. Silica particles, combined with W/O surfactant, have no effect on interfacial tension, which is only dictated by the surfactant concentration, while they strongly affect interfacial tension when combined with O/W surfactants. At low O/W surfactant, both particles and surfactant are adsorbed at the interface, modifying the interface structure. At higher concentration, interfacial tension is only dictated by the surfactant. By increasing the surfactant concentration, the contact angle that a drop of aqueous phase assumes on a glass substrate placed in oil media decreases or increases depending on whether the surfactant is of W/O or O/W type, respectively. This is due to the modification of the wettability of the glass by the oil or water induced by the surfactants. Regardless of the surfactant's type, the contact angle profile was dictated by both particles and surfactant at low surfactant concentration, whereas it is dictated by the surfactant only at high concentration. (C) 2012 Elsevier Inc. All rights reserved.
引用
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页码:396 / 405
页数:10
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