Nonaqueous foam with outstanding stability in diglycerol monomyristate/olive oil system

被引:40
作者
Shrestha, Rekha Goswami [1 ]
Shrestha, Lok Kumar [1 ]
Solans, Conxita [2 ]
Gonzalez, Carmen [3 ]
Aramaki, Kenji [1 ]
机构
[1] Yokohama Natl Univ, Grad Sch Environm & Informat Sci, Hodogaya Ku, Yokohama, Kanagawa 2408501, Japan
[2] CSIC, Spanish Council Sci Res, Inst Adv Chem Catalonia IQAC, ES-08034 Barcelona, Spain
[3] Univ Barcelona, Dept Chem Engn, E-08028 Barcelona, Spain
基金
日本学术振兴会;
关键词
Diglycerol monomyristate; Nonaqueous foam; Foamability; Foam stability; alpha-Solid dispersion; Liquid crystal dispersion; FATTY-ACID ESTERS; LAMELLAR LIQUID-CRYSTAL; SURFACE RHEOLOGY; PHASE-BEHAVIOR; STABILIZATION; PARTICLES; FILMS; WATER;
D O I
10.1016/j.colsurfa.2009.11.007
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
We report the formation of nonaqueous foam with outstanding stability in diglycerol monomyristate (designated as C(14)G(2)) nonionic surfactant in olive oil at 25 degrees C. Effects of surfactant concentration and added water on foamability and foam stability have been investigated. The C14G2 forms the dispersion of surfactant solid in the dilute surfactant concentration regions at 25 degrees C and they are responsible for the outstanding stability of nonaqueous foams, as they tend to adsorb at the gas-liquid interface. It was found that foamability increases with surfactant concentration up to a certain point, and then level off. In the case of water added system, the foamability increases monotonically with the concentration of water added. Foam stability studies have shown that the foams are stable for a few minutes to several weeks depending on the surfactant concentration and amount of added water. Foam was stable for similar to 20 min in 1 wt% C(14)G(2)/olive oil system, but it was stable more than a month in 10 wt% system. Foam stability of 5 wt% C14G2/olive oil system was decreased upon addition of 1 wt% water; foam was stable only for similar to 1.5 h. It was found that the average size of the surfactant solid decreases with increasing surfactant concentration and thus foams with better stability could be observed at higher concentrations. The poor foam stability in the water added systems was caused due to structural transition of surfactant solid (alpha-solid) to lamellar liquid crystalline phase. The present results are obtained by optical microscopy, surface tension, and rheology data. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:157 / 165
页数:9
相关论文
共 45 条
[21]  
Morrison I.D., 2002, COLLOIDAL DISPERSION
[22]   Foam stability: proteins and nanoparticles [J].
Murray, BS ;
Ettelaie, R .
CURRENT OPINION IN COLLOID & INTERFACE SCIENCE, 2004, 9 (05) :314-320
[23]  
OTTEWILL RH, 1981, CHEM IND-LONDON, P57
[24]   SURFACE RHEOLOGY AND PRACTICAL BEHAVIOR OF FOAMS AND THIN LIQUID-FILMS [J].
PRINS, A .
CHEMIE INGENIEUR TECHNIK, 1992, 64 (01) :73-75
[25]  
Prudhomme R., 1996, Foams: Theory, Measurements, and Applications
[26]   Foaming, foam films, antifoaming and defoaming [J].
Pugh, RJ .
ADVANCES IN COLLOID AND INTERFACE SCIENCE, 1996, 64 :67-142
[27]  
SADOC JF, 1999, NATO ASI SERIES E, V354
[28]   CRITICAL THICKNESS OF RUPTURE OF CHLORBENZENE AND ANILINE FILMS [J].
SCHELUDKO, A ;
MANEV, E .
TRANSACTIONS OF THE FARADAY SOCIETY, 1968, 64 (544P) :1123-+
[29]  
Scheludko A., 1967, Adv. Colloid Interface Sci, V1, P391, DOI DOI 10.1016/0001-8686(67)85001-2
[30]   Intrinsically superhydrophobic organosilica sol-gel foams [J].
Shirtcliffe, NJ ;
McHale, G ;
Newton, MI ;
Perry, CC .
LANGMUIR, 2003, 19 (14) :5626-5631