Thermodynamics of mixed anionic/nonionic surfactant adsorption on alumina

被引:22
|
作者
Lopata, Jeffrey J.
Werts, Kendall M.
Scamehorn, John F.
Harwell, Jeffrey H.
Grady, Brian P. [1 ]
机构
[1] Univ Oklahoma, Inst Appl Surfactant Res, Norman, OK 73019 USA
基金
美国国家科学基金会;
关键词
Surfactant adsorption; Regular solution theory; Mixed micelle; Surfactant; Surfactant mixtures; MINERAL OXIDE SURFACES; SODIUM DODECYL-SULFATE; FERRIC HYDRO SOLS; NONIONIC SURFACTANTS; ANIONIC SURFACTANTS; AQUEOUS-SOLUTIONS; WATER INTERFACE; FLUOROCARBON SURFACTANTS; BINARY-MIXTURES; BILAYERS;
D O I
10.1016/j.jcis.2009.10.072
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 adsorption of sodium dodecyl Sulfate and a polyethoxylated nonylphenol, and well defined mixtures thereof, was measured on gamma-alumina. A pseudo-phase separation model to describe mixed anionic/nonionic admicelle (adsorbed surfactant aggregate) formation was developed, analogous to the pseudophase separation model frequently used to describe mixed micelle formation. In this model, regular solution theory was used to describe the anionic/nonionic surfactant interactions in the mixed admicelle and a patch-wise adsorption model was used to describe surfactant adsorption on a heterogeneous solid surface. The formation of mixed anionic/nonionic admicelles in the absence of micelles was accurately described by regular solution theory; mixed admicelle formation exhibited stronger negative deviations from ideality than mixed micelle formation. An adequate description of mixed anionic/nonionic admicelle formation in the presence of mixed micelles was obtained through a simultaneous solution of the pseudo-phase separation models for mixed admicelle and mixed micelle formation, and the appropriate mass balance equations. Anionic/nonionic mixed adsorption in the presence of mixed micelles was shown to correspond to an admicelle composition of approximately a 1:1 anionic/nonionic mole ratio throughout Regions II and III of the adsorption isotherm. Published by Elsevier Inc.
引用
收藏
页码:415 / 426
页数:12
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