Emulsion stability in sucrose monoalkanoate system with addition of cosurfactants

被引:0
|
作者
Md. Kabir
M. Ishitobi
H. Kunieda
机构
[1] Graduate School of Environment and Information Sciences,
[2] Yokohama National University,undefined
[3] Tokiwadai 79–7,undefined
[4] Hodogaya-ku,undefined
[5] Yokohama 240–8501,undefined
[6] Japan,undefined
[7] Food Ingredients Laboratory,undefined
[8] Speciality Chemicals Research Center,undefined
[9] Mitsubishi Chemical Co.,undefined
[10] 1000,undefined
[11] Kamoshida-cho,undefined
[12] Aoba-ku,undefined
[13] Yokohama 227–8502,undefined
[14] Japan,undefined
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关键词
Sucrose monododecanoate Middle-phase microemulsion LC-present region Cosurfactant HLB;
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摘要
The hydrophile-lipophile property of the sucrose monododecanoate changes from hydrophilic to lipophilic by adding an alcohol as a cosurfactant. With the addition of a short-alkyl-chain alcohol (pentanol, hexanol), the surfactant forms the middle-phase microemulsion whereas a lamellar liquid crystal (Lα) appears with a medium- or long-chain alcohol (heptanol, octanol, decanol) at the balanced state in water/ SE/ cosurfactant/ decane system. The effect of changing oil was also studied in the presence of a middle-chain cosurfactant (heptanol). A short-chain aromatic oil (m-xylene) forms middle-phase microemulsion whereas a longer aliphatic one (hexadecane) forms lamellar liquid crystalline phase in a dilute region when the HLB of surfactant is balanced in a given system. O/W emulsions become stable on the hydrophilic-surfactant-rich side whereas W/O emulsions are stable on the cosurfactant-rich side. Emulsions are very unstable in the three-phase regions. However, when the lamellar phase is produced, emulsions become stable at the balanced state because water and oil are incorporated in Lα phase in the longer cosurfactant systems such as water/ SE/ octanol/ decane and water/ SE/ decanol/ decane.
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页码:841 / 847
页数:6
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