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  • 1
    ISSN: 1572-8927
    Keywords: Aprotic solvents ; association of ions ; conductance ; dissociation ; hydrochloric acid ; ionization ; ion-solvent interactions ; sulfolane
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The molar conductance of solutions of HCl (concentrations from 3×10−4 to 0.033 mol-l−1) in water-sulfolane (tetramethylenesulfone) mixtures of mole fractions (X2) of sulfolane of 0.25, 0.50, 0.75, and 0.85 at 25, 30, and 40°C have been determined. The dielectric constants of the solvents varied from 45 to 60 at 25°C. The data were analyzed by the full Pitts equation, the expanded Pitts equation, and the expanded Fuoss-Hsia equations, all of which give comparable results for the limiting molar conductanceA o and for the ion-pair association constant KA for HCl. These equations were unsuccessful for the analysis of supplemental data in pure sulfolane. At 25°C, the pK for dissociation of HCl varies from 0.4 (X2=0.25) to 2.9 (X2=0.85). The extent of ion pairing is apparently strongly influenced by selective ion-solvent interactions.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 29 (2000), S. 237-253 
    ISSN: 1572-8927
    Keywords: Conductivity ; electrolytes ; electrolyte theory
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Conductivity equations, based on the mean spherical approximation (MSA), haverecently been derived. We compare their performance with that of classicalequations at the level of experimental uncertainty using conductivity data forsome typical electrolyte solutions. For symmetrical electrolytes, the pictureisconsistent showing a better performance for the classical equations. The Leeand Wheaton equation also shows advantages at moderate concentrations. Forunsymmetrical electrolytes, the differences between MSA and classical equationsis larger. There is, however, an inherent inconsistency with the equilibriuminformation, which cannot be resolved at present.
    Type of Medium: Electronic Resource
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