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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 276 (1998), S. 52-58 
    ISSN: 1435-1536
    Keywords: Key words Dodecanephosphonic acid ; soluble monolayer ; air/water interface ; evaporation ; adsorption ; ion-selective 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 air/water interface of the system n-dodecanephosphonic acid (H2DP)–water was studied by surface tension, ion-selective electrodes and evaporation in an electrobalance. The combination of surface tension and ion-selective electrodes measurements enables to study the adsorption of soluble surfactants above the cmc using the Gibbs’ equation. H2DP formed a nonideal monolayer at the air/water interface with A molec=0.995 nm2 below the cmc. Above the cmc there was a reduction in adsorption giving A molec=6.32 nm2, which remained almost constant in the explored concentration range. This adsorption reduction may be due to a change composition on micellization, or to a thermodynamic advantage of micellization on adsorption. The reduction in the evaporation rate of water was mainly due to the reduction of the water activity, caused by the presence of solutes in bulk. This is because the strong changes in the surface coverage did not have significant influence on the evaporation rate.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1435-1536
    Keywords: Key words Dodecyltrimethyl-ammonium hydroxide ; soluble monolayer ; air/water interface ; evaporation ; ion-selective 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 system dodecyltrimethylammonium hydroxide (DTAOH)–water was studied by surface tension, ion-selective electrodes and evaporation in an electrobalance. Results confirmed earlier conclusions about a stepwise aggregation mechanism in DTAOH solutions. The aggregation process started at a total concentration C T=(2.51±0.10)×10-4 mol dm-3) which probably corresponds to the formation of dimers. At C T= (1.300±0.041)×10-3 mol dm-3 there was a change in the surface and evaporation behavior, corresponding to the formation of small, fully ionized aggregates which grew with increasing concentration. At C T= (1.108±0.010)×10-2 mol dm-3 the formation of true micelles with hydroxide counterions in the Stern layer did not change significantly the evaporation and adsorption behavior. This means that between this concentration and C T=(3.02±0.28)× M28.8n10-2 mol dm-3, the changes in structure were gradual. At the latter concentration there was a sudden change in the monolayer state at the air/water interface, with a strong surfactant desorption, and a major change in evaporation behavior. The changes are compatible with the formation of few, large aggregates reducing the total concentration of kinetically independent solute units, which in turn increased the activity of the solvent. This phenomenon is in agreement with literature information. The reduction in the evaporation rate of water was mainly due to the reduction of the water activity, caused by colligative effects. The reduction of the effective area available for evaporation had only a slight effect in water evaporation.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 273 (1995), S. 439-443 
    ISSN: 1435-1536
    Keywords: Surfactants ; evaporation ; inverse micelles ; microemulsions ; aerosol OT
    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 evaporation rate of aerosol OT-water-n-heptane inverse micellar systems was studied. The evaporation behavior of solutions was strongly affected when compared with pure heptane. The changes are related to the structure of the micelles and the properties of the water molecules dissolved in the micelles. The initial rate of evaporation reaches a maximum when the surfactant head groups are hydrated with three water molecules, a minimum when the first hydration shell of Na+ ions is completed, and then rises and stabilizes until the second hydration shell is completed. The presence of free water when the ratio water molecules to surfactant molecules exceeds 12 produces a new rise of the initial evaporation rate, which is always higher than that of puren-heptane.
    Type of Medium: Electronic Resource
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