Surfactant-free O/W emulsion formation of oleic acid and its esters with ultrasonic dispersion

被引:49
|
作者
Kamogawa, K
Akatsuka, H
Matsumoto, M
Yokoyama, S
Sakai, T
Sakai, H
Abe, M
机构
[1] Sci Univ Tokyo, Inst Colloid & Interface Sci, Shinjuku Ku, Tokyo 1628601, Japan
[2] Minist Educ Sci Sports & Culture, Ele & Sec Ed Bur, Chiyoda Ku, Tokyo 1000013, Japan
[3] Sci Univ Tokyo, Fac Sci & Technol, Noda, Chiba 2788510, Japan
[4] Kyoritsu Coll Pharm, Minato Ku, Tokyo 1058512, Japan
关键词
surfactant-free emulsion; oleic acid and its esters; growth mechanism;
D O I
10.1016/S0927-7757(00)00758-5
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
Dispersibility and stabilizing factors for surfactant-free O/W emulsion were investigated with oleic acid (OA) and its esters, focusing on the effects of their weak polarity, molecular length and branched chain structure, in comparison to normal hydrocarbons. The droplet size distributions obtained by the dynamic light scattering method appeared to be discrete but almost singly peaked except for OA. For OA monoesters, the droplet growth was found to be continuous and retarded as the ester chain length increased, in contrast to the discrete, fast growth in OA dispersion. In the case of glycerol trioleate (GTO), a branched ester, aqueous dispersions of extremely fine droplets could be prepared and the number distribution of droplet diameters showed a single peak in the nanometer range. This high dispersibility remained unchanged for about a year after preparation to give the dispersions a good stability. Changes of the observed xi potential, Fourier transform-infra red (FT-IR) spectrum, fluorescence spectrum of probes indicated that a particular carboxyl acid group network is formed in the droplet sphere to make it more stable than expected while the interior of oil droplets is hydrophobic. The xi potential change, in particular, was found to be highly correlated with these of the carboxyl C=O stretching frequency and the reciprocal droplet diameter. The droplet stability evaluated by increase in the diameter revealed a biphasic growth consisting of fast and slow modes. The fast growth at early stages tin hours) observed for OA and methyl oleate (MO) was found to proceed by the Ostwald ripening mechanism through rate analysis. On the other hand, the slow growth at later stages tin days) found for the other esters showed a semi-logarithmic dependence on the oil viscosity. This seems to be caused by an Arrhenius-type activation factor in the stepwise flocculation/coalescence rate. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:41 / 53
页数:13
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