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  • Electronic Resource  (4)
  • sodium alkyl sulfates  (2)
  • sodium dodecyl sulfate  (2)
  • 1
    ISSN: 1435-1536
    Keywords: Criticalmicelle concentration ; aggregation number ; sodium alkyl sulfates ; isotachophoresis ; PU value
    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 analytical procedure for the separation and quantification of bulk and micellar phases for sodium alkyl sulfates has been investigated by a capillary-type isotachophoresis using a potential gradient detector. Monomer solutions were distinguished from micellar solutions at pH 5.5–6.0; hydrochloric acid — L-Histidine mixture was used as the leading electrolyte and 2-(N-Morpholino) ethanesulfonic acid as the terminating electrolyte. The potential unit value (PU value) due to the monomer solutions was larger than that due to the micellar solutions. The zone length due to monomer solutions increased with increasing concentration of surfactant until a given concentration (CMC); beyond this point the values became constant. On the other hand, the zone length due to micellar solutions increased from this point. We report an applicability of capillary-type isotachophoresis to determination of the CMC's and aggregation number for various sodium alkyl sulfates.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 262 (1984), S. 657-661 
    ISSN: 1435-1536
    Keywords: azo oil dye ; electron charge transfer complex ; sodium alkyl sulfates ; protonation equilibrium ; thermochromism
    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 between 4-phenylazo-1-naphthylamine and 6 sodium alkyl sulfates have been studied by a spectrophotometer. At lower concentrations than each CMC, 3 surfactants (octyl, decyl and dodecyl sulfate) and the dye formed hydrophobic complexes with a binding molar ratio of 1∶1, while the others (tetradecyl, hexadecyl, and octadecyl sulfate) and the dye made 2∶1 complexes. The wavelength of the maximal absorption is 440 nm in the former, and 520 nm in the latter. In the neighborhood of each CMC region, thermochromism occurred in every surfactant solution. The temperature at which the maximal absorption moved from 520 nm to 440 nm increased with an increase in the number of carbon atoms in the surfactant molecules. At higher concentrations than each CMC, in the case of the octyl and decyl sulfate, the maximal absorption occurred at the 440 nm band above room temperature; in the case of the dodecyl, tetradecyl, and hexadecyl sulfates, the maximal absorption occurred at the 520 nm band, regardless of temperature. In the case of octadecyl sulfate, the maximal absorption moved from 610 nm to 520 nm with increase in temperature. It is found that the protonation equilibrium of the dye is dependent on the micellar structure through the differences in the alkyl chain lengths of the surfactants, and the differences in interaction with surfactant crystals.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 266 (1988), S. 539-546 
    ISSN: 1435-1536
    Keywords: Surfactant-dye complex ; sodium dodecyl sulfate ; azo oil dye ; thermodynamics study ; dyeing rate
    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 Spectrophotometric and thermodynamic investigations are reported of the interactions between anionic surfactant (sodium dodecyl sulfate) and six azo oil dyes (benzene azo naphthalene type) which have an amino group at 4-position of naphthalene. A pronounced spectral change in the dye solution occurs on addition of surfactant. For increasingly surfactant concentrations (below the CMC), the interaction between dye and surfactant is so sharp that the systems may be said to exhibit an isosbestic point; then a new absorption band appears at longer wavelengths. The spectral data can be quantitatively interpreted in terms of a complex formation. The equilibrium coefficients of the complex formation are determined at different temperatures. The thermodynamic parameters of the complex formations (the free energy change (ΔG), enthalpy change (ΔH) and change in entropy (ΔS) are also calculated. The reaction of complex formation is exothermic (ΔH negative).ΔG is dependent on the hydrophobic nature andpKa of the dye. These complexes will form due to hydrophilic-hydrophilic interaction and will become more stable due to hydrophobic-hydrophobic interaction. With increasing amounts of complex, the infinite adsorption, the exhaustion and the rate constant of dyeing for nylon decrease.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Colloid & polymer science 264 (1986), S. 1085-1089 
    ISSN: 1435-1536
    Keywords: Adsorption ; activated carbon ; surfactants ; sodium dodecyl sulfate ; polyoxyethylene hexadecyl ether
    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 This study shows how trace amounts of surfactants are adsorbed by activated carbon under competitive conditions in aqueous solution. Surfactants used as adsorbates are sodium dodecyl sulfate (SDS) and eicosaneoxyethylene hexadecyl ether (POE). Activated carbon used as an adsorbent is Pittsburgh activated carbon. Adsorption isotherms on the activated carbon were all Freundlich-type, both in the multi-solute system and in the mono-solute systems. The total adsorbed amount in the multi-solute system increases linearly with increasing molar fraction of SDS in the initial concentration. Thus, the total adsorbed amount in the multi-solute system can be estimated by the Freundlich constants, which can be determined from the single-solute equilibrium adsorptions, and molar fractions of adsorbates in the initial concentration.
    Type of Medium: Electronic Resource
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