PHASE-BEHAVIOR OF AN IONIC MICROEMULSION SYSTEM AS A FUNCTION OF THE COSURFACTANT CHAIN-LENGTH

被引:33
作者
KEGEL, WK [1 ]
LEKKERKERKER, HNW [1 ]
机构
[1] UNIV UTRECHT,VANT HOFF LAB,PADUALAAN 8,3584 CH UTRECHT,NETHERLANDS
关键词
COSURFACTANT CHAIN LENGTH; IONIC MICROEMULSION; PHASE BEHAVIOR;
D O I
10.1016/0927-7757(93)80084-R
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 phase behaviour of a microemulsion system consisting of equal volumes of brine and oil, sodium dodecyl sulphate (SDS) as surfactant and alcohols of different chain lengths (pentanol, hexanol and heptanol) as cosurfactant was studied. In the case of pentanol, at low surfactant concentrations and increasing alcohol concentration, the well-known progression of phase equilibria, Winsor I-Winsor III-Winsor II, was observed. The use of hexanol or heptanol as cosurfactant leads to rather different phase behaviour. At low surfactant concentrations and increasing alcohol concentration the following sequence of phase equilibria is observed: Winsor I-Winsor III-four-phase equilibrium (water-lamellar phase-isotropic microemulsion phase-oil)-Winsor III-Winsor II. Increasing the surfactant concentration starting from the four-phase equilibrium first leads to a three-phase equilibrium (lamellar phase-isotropic microemulsion-oil), then a two-phase equilibrium (lamellar-bicontinuous microemulsion) followed by a monophasic lamellar system. The observed change in phase behaviour as a function of the cosurfactant chain length is discussed in terms of phenomenological interfacial models of microemulsions.
引用
收藏
页码:241 / 248
页数:8
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