The surfactant system tetradecyldimethylamine oxide (TDMAO)/ benzyl alcohol/water has been studied. In the phase diagram of this ternary system a large isotropic region is encountered that connects the water corner to the benzyl alcohol corner. This isotropic phase has been investigated in some deta
Structural Changes Induced in the Surfactant System C12E4/Benzyl Alcohol/Water by the Admixture of the Cationic Surfactant Cetylpyridinium Chloride
โ Scribed by G. Montalvo; M. Valiente; K. Mortensen; M. Gradzielski
- Publisher
- Elsevier Science
- Year
- 2001
- Tongue
- English
- Weight
- 174 KB
- Volume
- 238
- Category
- Article
- ISSN
- 0021-9797
No coin nor oath required. For personal study only.
โฆ Synopsis
The influence of the addition of the cationic surfactant cetylpyridinium chloride (CPyCl) on the structure of the different phases of the ternary surfactant system C 12 E 4 /benzyl alcohol/water in the dilute region has been studied by means of small angle neutron scattering (SANS) and freeze-fracture microscopy (FF-TEM). In the ternary system various different subregions of the L ฮฑ -phase were identified as a function of the concentration of the cosurfactant, benzyl alcohol. Addition of small amounts of CPyCl suppresses these different L ฮฑ -phases in favor of the one composed of multilamellar vesicles. Addition of somewhat larger amounts (up to 2 mol% relative to the total surfactant concentration) destabilizes the formation of bilayer structures completely and leads to the formation of micellar solutions. This demonstrates that in this surfactant system the incorporation of very small amounts of cationic surfactant has a pronounced and systematic fluence on its phase behavior and its structures.
๐ SIMILAR VOLUMES
The influence of a small amount of cetylpyridinium chloride on the phase diagram of the diluted C 12 E 4 /benzyl alcohol/water system is studied. The presence of the ionic surfactant results in the stabilization of the vesicles in relation to the open bilayers. The bilayer structures are less sensit