Micelle formation was studied for four mixing combinations of dodecylammonium (DA) salts having perfluorocarboxylate ions (trifluoroacetate (PA) and pentafluoropropionate (PP) and alkane sulfonate ions (methane sulfonate (MS) and ethane sulfonate (ES)) as their counterions, i.e., DAPA/DAMS, DAPA/DAE
Micelle Formation of Anionic Surfactant with Divalent Counterion of Separate Electric Charge
โ Scribed by Takaharu Yamabe; Yoshikiyo Moroi
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 92 KB
- Volume
- 215
- Category
- Article
- ISSN
- 0021-9797
No coin nor oath required. For personal study only.
โฆ Synopsis
The critical micelle concentration (CMC) of the anionic surfactant, 1,1'-(1,omega-decanediyl) bispyridinium hexadecane-1-sulfonate (C10BP(C16)2) was determined by electrical conductivity measurements at various temperatures. The degree of counterion binding to micelles was evaluated from the change in CMC with total counterion concentration. The molecular weight of the micelles was determined by static light scattering. The mass action model was applied to micelle formation in order to calculate the three micellization parameters, the micellization constant, the micelle aggregation number, and the number of counterions per micelle. Thermodynamic parameters (DeltaG0, DeltaH0, -TDeltaS0) for the micellization were evaluated by their temperature dependence. The findings were: (1) Micelle formation was entropy-driven over the whole temperature range examined. (2) C10BP(C16)2 had a higher degree of counterion binding to micelles compared with those of monovalent counterion. (3) The plots of log CMC against the carbon number of the homologous surfactant ions gave a straight line, indicating that free energy change per methylene group for micelle formation was -1.18RT for surfactant ions. Copyright 1999 Academic Press.
๐ SIMILAR VOLUMES
## Abstract This report is an extension of our previous work involving the development of __in situ__ charged micellar phases with adjustable surface charge density for micellar electrokinetic capillary chromatography (MECC) of neutral and charged herbicides. The micelles evaluated here are basical