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  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 273 (1995), S. 959-966 
    ISSN: 1435-1536
    Keywords: Hydroxide surfactants ; critical micelle concentration ; aggregation ; cationic surfactants ; micelle charge
    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 aggregation of dodecyltrimethylammonium hydroxide (DTAOH) aqueous solutions has been studied by several methods. It is stepwise and four critical points were found. AtC T=(2.51±0.10)×10−4 mol · dm−3 the surface excess becomes zero, atC T=(1.300±0.041)×10−3 mol · dm−3 small aggregates from, which grow with concentration. AtC T=(1.108±0.010)×10−2 mol · dm−3 true micelles form (CMC) and at (3.02±0.28)×10−2 mol · dm−3 the structure of micelles probably changes affecting their properties. The DTAOH micelles are highly ionized (α=0.8) at the CMC, and decreases to reach very small values when the total concentration increases.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 274 (1996), S. 669-677 
    ISSN: 1435-1536
    Keywords: Dodecanephosphonic acid ; dodecyltrimethylammonium hydroxide ; mixed micelles ; critical micelle concentration ; aggregation
    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 aggregation of aqueous dodecylphosphonic acid (DPA) and dodecyltrimethylammonium hydroxide (DTAOH) mixtures was studied by several methods. The behavior of DPA-rich mixtures is close to that of pure DPA. This is probably due to the preservation of the hydrogen-bonded structure of the micellar headgroup layer. The behavior is almost ideal. Betweeny DPA =0.5 and 0.33 (y DPA being the mole fraction of DPA in the surfactant mixture), the hydrogen-bonded structure of the micellar headgroup layer is destroyed. A sort of “micellar azeotrope” is formed, and the maximum of non-ideal interaction between the two surfactants is attained aty DPA =0.4. Fory DPA 〈0.33 the system behaves as a common mixture of a cationic surfactant and a non-ionic one (DPA.2LTA). There is a phenomenon of counterion “condensation” on aggregates at concentrations over the CMC.
    Type of Medium: Electronic Resource
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  • 3
    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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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 274 (1996), S. 854-859 
    ISSN: 1435-1536
    Keywords: Hydroxide surfactants ; critical micelle concentration ; aggregation ; cationic surfactants ; counterion effect
    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 aggregation of dodecyltrimethylammonium hydroxide (DTAOH) in aqueous NaOH solutions was studied as a function of NaOH concentration. As in NaOH-free DTAOH aqueous solutions, the surfactant underwent a stepwise aggregation mechanism. Changes in the structure of aggregates produced an increase of the concentration at which premicellar aggregates could solubilize hydrophobic dyes and also in the concentration at which hydroxide inons join the aggregates.
    Type of Medium: Electronic Resource
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  • 5
    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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