Structure and extent of adsorbed gelatin on acrylic latex and polystyrene colloidal particles

被引:43
|
作者
Vaynberg, KA
Wagner, NJ [1 ]
Sharma, R
Martic, P
机构
[1] Univ Delaware, Dept Chem Engn, Ctr Mol & Engn Thermodynam, Newark, DE 19716 USA
[2] Eastman Kodak Co, Res Labs, Rochester, NY 14650 USA
基金
美国国家科学基金会;
关键词
gelatin; colloids; interfacial structure; forces; adsorption isotherms; dynamic light scattering; small-angle neutron scattering; dilution viscometry;
D O I
10.1006/jcis.1998.5640
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 extent and structure of the adsorbed layer of gelatin onto colloidal particles is measured using dynamic light scattering, small-angle neutron scattering, and dilution viscometry. Adsorption isotherms are measured using solution depletion of fluorescein-5-isothiocyanate tagged gelatin. The results show that the adsorbed gelatin layer at saturation on acrylic-based latex (pH 6.5, 0.01 M sodium acetate) has approximately twice the average density of the free gelatin in solution, while for the adsorption onto polystyrene latex (pH 8.7, deionized water), it has nearly the same average density. The energetics of gelatin affinity is calculated from the temperature dependence of the adsorption equilibrium constant. It was found that the enthalpy of adsorption of a net negatively charged gelatin onto a negatively charged surface is favorable. An additional, favorable entropy of adsorption is measured for the polystyrene latex, for which hydrophobic interactions are important. Selective, competitive adsorption of nonionic and anionic surfactants confirms the specific source of the adsorption interactions. (C) 1998 Academic Press.
引用
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页码:131 / 140
页数:10
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