EFFECT OF THE NATURE OF THE HYDROPHOBIC OIL PHASE AND SURFACTANT IN THE FORMATION OF CONCENTRATED EMULSIONS

被引:35
作者
CHEN, HH [1 ]
RUCKENSTEIN, E [1 ]
机构
[1] SUNY BUFFALO,DEPT CHEM ENGN,BUFFALO,NY 14260
关键词
D O I
10.1016/0021-9797(91)90117-Q
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
There exists a maximum amount of dispersed phase which can be incorporated into a concentrated emulsion. The experiments have been carried out with a large number of organic molecules as either the dispersed or the continuous phase and with water as the other phase, using several surfactants as dispersants. The maximum volume ratio between the dispersed and continuous phases ranged from 10 to 420, depending upon the natures of the organic molecule and surfactant. Generally, it was found, for both O W and W O systems, that the maximum volume ratio increases as the interfacial free energy, γwo, between the organic compound and water in the absence of surfactant increases. The aromatic and halogenated molecules exhibited deviations from this rule, when nonionic surfactants with polyoxyethylene head groups were employed, because of their interactions with the head groups of the surfactants. For ionic surfactants in O W systems, it was found that the curve of maximum volume ratio against γwo passes through a maximum at relatively large values of γwo. A possible explanation is suggested for this observation. For O W concentrated emulsions and two surfactants, one ionic and the other nonionic, experiments have been performed regarding the dependence of the maximum volume ratio upon the concentration of the surfactant. For the ionic surfactant, the curve exhibits saturation, while for the nonionic surfactant, it presents a maximum. © 1991.
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页码:260 / 269
页数:10
相关论文
共 18 条
[1]   NONIONIC SURFACE-ACTIVE COMPOUNDS .7. INTERFACIAL TENSIONS OF SOLUTIONS OF NONIONIC SURFACE-ACTIVE AGENTS [J].
BECHER, P .
JOURNAL OF COLLOID SCIENCE, 1963, 18 (07) :665-&
[2]   CORRELATION BETWEEN THE STABILITY OF CONCENTRATED EMULSIONS AND THE INTERFACIAL FREE-ENERGY BETWEEN THE 2 PHASES [J].
CHEN, HH ;
RUCKENSTEIN, E .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1990, 138 (02) :473-479
[3]  
DEAN JA, 1985, LANGES HDB CHEM, P103
[4]   A THEORY FOR THE ESTIMATION OF SURFACE AND INTERFACIAL ENERGIES .1. DERIVATION AND APPLICATION TO INTERFACIAL TENSION [J].
GIRIFALCO, LA ;
GOOD, RJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1957, 61 (07) :904-909
[5]  
Hirschfelder JO, 1954, MOL THEORY GASES LIQ
[6]  
LISANT KJ, 1972, J COLLOID INTERF SCI, V42, P201
[7]   HIGHLY CONCENTRATED EMULSIONS .2. REAL SYSTEMS THE EFFECT OF FILM THICKNESS AND CONTACT-ANGLE ON THE VOLUME FRACTION IN CREAMED EMULSIONS [J].
PRINCEN, HM ;
ARONSON, MP ;
MOSER, JC .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1980, 75 (01) :246-270
[8]   RHEOLOGY OF FOAMS AND HIGHLY CONCENTRATED EMULSIONS .4. AN EXPERIMENTAL-STUDY OF THE SHEAR VISCOSITY AND YIELD STRESS OF CONCENTRATED EMULSIONS [J].
PRINCEN, HM ;
KISS, AD .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1989, 128 (01) :176-187
[9]   STABILITY OF HYDROCARBON-IN-WATER EMULSIONS DURING CENTRIFUGATION - INFLUENCE OF DISPERSED PHASE COMPOSITION [J].
REHFELD, SJ .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1974, 46 (03) :448-459
[10]   ADSORPTION OF SODIUM DODECYL SULFATE AT VARIOUS HYDROCARBON-WATER INTERFACES [J].
REHFELD, SJ .
JOURNAL OF PHYSICAL CHEMISTRY, 1967, 71 (03) :738-&