Further studies on the effect of degassing on the dispersion and stability of surfactant-free emulsions

被引:71
作者
Maeda, N [1 ]
Rosenberg, KJ
Israelachvili, JN
Pashley, RM
机构
[1] Univ Calif Santa Barbara, Dept Chem Engn, Santa Barbara, CA 93106 USA
[2] Univ Calif Santa Barbara, Dept Phys, Santa Barbara, CA 93106 USA
[3] Australian Natl Univ, Dept Chem, Canberra, ACT 0200, Australia
关键词
D O I
10.1021/la036028g
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Recently reported results indicate that the formation of surfactant-free, oil-in-water emulsions can be significantly enhanced by the almost complete removal of dissolved gases and that the reintroduction of dissolved gases does not immediately destabilize the already-formed emulsions. These initial experiments have been repeated and extended to include a wider range of organic liquids and the application of light scattering to determine droplet size and distribution. The earlier observations have been confirmed. In addition, a systematic trend was found between the solubility of the oil in water and the stability (lifetime) of the degassed oil droplets in water. The lower the solubility, the more stable the emulsion, and for oils that are sparingly soluble in water such as squalane, the small droplets remain stable for several weeks, with buoyancy separation being the main cause of instability of the large droplets with time. The addition of electrolytes, up to molar concentrations, substantially reduces the enhancement of the dispersions on degassing but appears to have little effect on the stability of the already-formed emulsions. The reduction of pH to about 2 significantly reduces both the enhancement of the dispersions on degassing and the stability of the already-formed emulsions. In contrast, the increase of pH to about 11 hardly affects the enhancement of the dispersions on degassing or the stability of the already-formed emulsions. We have confirmed the importance of dissolved gas and its association with the electrostatic effects, but we still cannot provide a complete explanation for the effect of degassing on the hydrophobic dispersions.
引用
收藏
页码:3129 / 3137
页数:9
相关论文
共 17 条
[1]   Fluorescence study of the aggregation behavior of different surfactants in aqueous solutions in the presence and in the absence of gas [J].
Alargova, RG ;
Kochijashky, II ;
Zana, R .
LANGMUIR, 1998, 14 (07) :1575-1579
[2]   Effect of salts and dissolved gas on optical cavitation near hydrophobic and hydrophilic surfaces [J].
Bunkin, NF ;
Kiseleva, OA ;
Lobeyev, AV ;
Movchan, TG ;
Ninham, BW ;
Vinogradova, OI .
LANGMUIR, 1997, 13 (11) :3024-3028
[3]   Direct measurements of the force between hydrophobic surfaces in water [J].
Christenson, HK ;
Claesson, PM .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 2001, 91 (03) :391-436
[4]   EFFECT OF ELECTROLYTES ON BUBBLE COALESCENCE [J].
CRAIG, VSJ ;
NINHAM, BW ;
PASHLEY, RM .
NATURE, 1993, 364 (6435) :317-319
[5]   THE EFFECT OF ELECTROLYTES ON BUBBLE COALESCENCE IN WATER [J].
CRAIG, VSJ ;
NINHAM, BW ;
PASHLEY, RM .
JOURNAL OF PHYSICAL CHEMISTRY, 1993, 97 (39) :10192-10197
[6]  
CRANK J, 1975, MATH DIFFUSION, P13108
[7]  
FRIBERG SE, 1996, EMULSIONS EMULSION S, P13108
[8]   ROLE OF HYDROPHOBIC FORCES IN BILAYER ADHESION AND FUSION [J].
HELM, CA ;
ISRAELACHVILI, JN ;
MCGUIGGAN, PM .
BIOCHEMISTRY, 1992, 31 (06) :1794-1805
[9]   Attraction between hydrophobic surfaces with and without gas phase [J].
Ishida, N ;
Sakamoto, M ;
Miyahara, M ;
Higashitani, K .
LANGMUIR, 2000, 16 (13) :5681-5687
[10]   THE HYDROPHOBIC INTERACTION IS LONG-RANGE, DECAYING EXPONENTIALLY WITH DISTANCE [J].
ISRAELACHVILI, J ;
PASHLEY, R .
NATURE, 1982, 300 (5890) :341-342