Effect of added salt on three-phase behavior in a sucrose monoalkanoate system

被引:31
作者
Aramaki, K
Kunieda, H
Ishitobi, M
Tagawa, T
机构
[1] YOKOHAMA NATL UNIV,GRAD SCH ENGN,DIV ARTIFICIAL ENVIRONM SYST,HODOGAYA KU,YOKOHAMA,KANAGAWA 240,JAPAN
[2] MITSUBISHI CHEM CORP,YOKOHAMA RES CTR,R&D DIV,AOBA KU,YOKOHAMA,KANAGAWA 227,JAPAN
关键词
D O I
10.1021/la961067w
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Effect of added salt on the three-phase behavior of microemulsion in water/octaethylene glycol dodecyl ether (C12EO8)hexanol/decane and water/sucrose monododecanoate (SMD)/hexanol/decane systems was investigated at 25 degrees C. The three-phase body is shifted to higher hexanol mixing ratio upon addition of KSCN, whereas the opposite tendency is observed upon addition of NaCl in the C12EO8 system. These phenomena can be explained by salting-out and salting-in effects, respectively. On the other hand, the three-phase body is shifted to higher hexanol mixing ratio upon addition of both inorganic salts in the SMD system. In the absence of oil, however, the effect of added salt on the clouding phenomena in the SMD system is similar to that in the C12EO8 system. The mixing fraction of hexanol in the total surfactant (nonionic surfactant + hexanol) in the interface of micro-oil and water domains inside the middle-phase microemulsion is estimated according to the geometrical relation of a three-phase body in the space of compositions. As st result, the effect of added inorganic salt on the mixing fraction in the interface is opposite to that on the apparent mixing fraction of hexanol in the total surfactant to form the three-phase body in the SMD system. Consequently, this novel phenomenon can be explained by the change in the nature of excess oil phase or micro-oil domain due to the high solubility of hexanol in oil.
引用
收藏
页码:2266 / 2270
页数:5
相关论文
共 26 条
[1]   PROPERTIES AND STRUCTURE OF 3-COMPONENT IONIC MICROEMULSIONS [J].
CHEN, SJ ;
EVANS, DF ;
NINHAM, BW .
JOURNAL OF PHYSICAL CHEMISTRY, 1984, 88 (08) :1631-1634
[2]   ELECTROLYTE EFFECTS ON MICELLAR SOLUTIONS OF NONIONIC DETERGENTS [J].
DOREN, A ;
GOLDFARB, J .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1970, 32 (01) :67-&
[3]   ENTHALPIES OF SOLUTION OF HEXAN-1-OL AND HEPTAN-1-OL IN WATER [J].
HILL, DJT ;
WHITE, LR .
AUSTRALIAN JOURNAL OF CHEMISTRY, 1974, 27 (09) :1905-1916
[4]   MICROSTRUCTURE OF MICROEMULSIONS BY FREEZE-FRACTURE ELECTRON-MICROSCOPY [J].
JAHN, W ;
STREY, R .
JOURNAL OF PHYSICAL CHEMISTRY, 1988, 92 (08) :2294-2301
[5]   SALT EFFECTS ON NONIONIC MICROEMULSIONS ARE DRIVEN BY ADSORPTION/DEPLETION AT THE SURFACTANT MONOLAYER [J].
KABALNOV, A ;
OLSSON, U ;
WENNERSTROM, H .
JOURNAL OF PHYSICAL CHEMISTRY, 1995, 99 (16) :6220-6230
[8]   CORRELATION BETWEEN CRITICAL SOLUTION PHENOMENA AND ULTRALOW INTERFACIAL-TENSIONS IN A SURFACTANT WATER OIL SYSTEM [J].
KUNIEDA, H ;
SHINODA, K .
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN, 1982, 55 (06) :1777-1781
[9]   3-PHASE BEHAVIOR IN A MIXED SUCROSE ALKANOATE AND POLYETHYLENEGLYCOL ALKYL ETHER SYSTEM [J].
KUNIEDA, H ;
USHIO, N ;
NAKANO, A ;
MIURA, M .
JOURNAL OF COLLOID AND INTERFACE SCIENCE, 1993, 159 (01) :37-44
[10]   Effect of added salt on the maximum solubilization in an ionic-surfactant microemulsion [J].
Kunieda, H ;
Aoki, R .
LANGMUIR, 1996, 12 (24) :5796-5799