The cis/trans conformational equilibrium of the two Ac-Pro isomers of the beta-turn model dipeptide [13C]-Ac-L-Pro-D-Ala-NHMe, 98% 13C enriched at the acetyl carbonyl atom, was investigated by the use of variable temperature gradient enhanced 1H-nmr, two-dimensional (2D) 1H,1H nuclear Overhauser eff
Counterion Effects in Aqueous Solutions of Cationic Surfactants: Electromotive Force Measurements and Thermodynamic Model
✍ Scribed by Laurent Gaillon; Joël Lelièvre; René Gaboriaud
- Publisher
- Elsevier Science
- Year
- 1999
- Tongue
- English
- Weight
- 123 KB
- Volume
- 213
- Category
- Article
- ISSN
- 0021-9797
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✦ Synopsis
EMF measurements have been performed to study the influence of counterions in aqueous solutions of ionic surfactants in which the amphiphile is an n-alkyltrimethylammonium cation. General rules of variation were observed for the activities of the amphiphilic ion and the counterion, as a function of the global concentration of the surfactant salt. This study also allows us to have access to the degree of counterion binding  over a wide range of counterions (bromide, chloride, fluoride, hydroxide, nitrate, acetate, benzoate). A systematic correlation between the concentrations of an amphiphilic cation and a counterion in solution has been established when the micellization process occurs. This correlation is also verified when a background electrolyte with a common anion is added to the surfactant solution. The mathematical relation translating the real link between concentrations of both ions of the micellar salt, deduced from this correlation, emphasizes the existence of a condition of micellization, in the form of a micellization product. A new thermodynamic model based on the electrochemical equilibrium of a dispersed phase (pseudo-phase) is developed, and we justify the existence of this condition of micellization or micellization product. Furthermore, this model is shown to be well adapted for the description of the whole phenomena observed in micellar solutions.
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