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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 277 (1999), S. 48-57 
    ISSN: 1435-1536
    Keywords: Key words Polyampholytes ; Ionic surfactants ; Polyampholyte- surfactant interactions ; Polymer-surfactant interactions ; Ion-specific electrodes
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The interactions of two partially charged ampholytic terpolymers [consisting of acrylamide, sodium 2-acrylamido-2-methylpropanesulphonate, and 2-(methacryloyloxyethyl)trimethylammonium chloride segments with molar compositions 80/12/08 and 80/08/12] and two fully charged ampholytic copolymers (containing only the two latter comonomers with molar compositions of 80/20 and 50/50), with cationic surfactants [tetradecyl- trimethylammonium bromide (TTAB) and cetyltrimethylammonium bromide (CTAB)] and the anionic surfactant sodium dodecylsulphate (SDS), are investigated. The studies include phase behaviour (swelling, solubilisation, precipitation), viscometry, electrical conductivity, and potentiometry (bromide ion and surfactant ion-specific electrodes). The 80/08/12 and 80/12/08 polyampholytes swell in water and are solubilised in the presence of cationic or anionic surfactants above a particular surfactant concentration that is proportional to the polymer concentration. The polyampolyte 80/20 is soluble in water but precipitates in the presence of TTAB, whereas 50/50 is insoluble in water and in the presence of TTAB, but is solubilised upon addition of SDS. The results indicate that TTAB binds to 80/12/08 with little or no cooperativity. Solubilisation appears to be the result of the increasing polyelectrolyte character of the polyampholyte upon neutralisation of its charged sites by bound surfactant ions of opposite charge. The binding of TTAB by the 50/50 polyampholyte is very weak and non-cooperative. In contrast, 80/20 binds TTAB cooperatively, much like a true polyelectrolyte-surfactant system of opposing charges. In particular, the binding is characterised by the existence of a critical aggregation concentration. A partial phase diagram for this system has been determined from the TTA+-electrode potential data. The behaviour of true polyelectrolytes and polyampholytes, with respect to their interaction with surfactants, is discussed.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1536
    Keywords: Ionic surfactants ; self-association ; formamide ; formic acid ; ethyleneglycol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology , Mechanical Engineering, Materials Science, Production Engineering, Mining and Metallurgy, Traffic Engineering, Precision Mechanics
    Notes: Abstract The self-association of several cationic surfactants has been investigated by means of solubility and electrical conductivityκ measurements in ethyleneglycol, formic acid and formamide. Operational critical micelle concentrations (CMCop) have been obtained from theκ vs. surfactant concentrationC plots by the usual interpolation procedure. It has been found that for the surfactant-solvent systems investigated the value of CMCop increases with the extent of theC-range investigated. This result together with others concerning the effect of temperature and surfactant chain length reveal that the CMCop-values have an ambiguous meaning concerning the surfactant self-association. Comparison of theκ vs.C plots for cetyltrimethylammonium chloride and tetramethylammonium chloride, for instance, reveals that some surfactant self-association takes place, probably leading to small, highly ionized surfactant aggregates, but the systems do not show true critical micelle concentration. Solubility measurements as a function of temperature lead to the same conclusion. The results are discussed according to our present understanding of the process of micellization and the necessity of using solvents of very high cohesive energy density in order to observe, with ionic surfactants, true CMCs corresponding to a highly cooperative association process. This appears to be the case only with water and hydrazine, not with formamide and other less cohesive solvents.
    Type of Medium: Electronic Resource
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