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  • water-dioxane  (2)
  • Dielectric constant  (1)
  • KClO3  (1)
  • 1
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 19 (1990), S. 1211-1224 
    ISSN: 1572-8927
    Keywords: Hydrochloric acid ; water-tetrahydrofuran ; water-dioxane ; water-dimethoxyethane ; conductance ; association constants ; proton mobility ; Gurney cosphere
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Conductance of dilute solutions of HCl in water-tetrahydrofuran (THF), water-dioxane and water-dimethoxyethane (DME) were measured and the data processed using the Justice-Ebeling equation to evaluate the limiting conductance ΛO, the association constant KA and the apparent distance of closest approach a'. The Friedman-Rasaiah Gurney cosphere overlap term d+−/kT was calculated from a' values and illustrates the different solvation pattern of dioxane compared to that found for THF and DME. It would appear that dioxane can solvate cations more strongly due to its ability to form a boat configuration around a cation. The association constants are reasonably reproduced by the Bjerrum equation using realistic molecular dimensions of the ions involved for the distance of closest approach. The limiting conductance in the mixtures illustrates clearly the different mechanism for proton conductance compared to that for the cesium ion. The dielectric constants, viscosities and densities of the solvent mixtures were measured and are reported. The lowest dielectric constant for each type of solvent mixture was about 10.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 4 (1975), S. 299-310 
    ISSN: 1572-8927
    Keywords: Dielectric constant ; ethanol ; high pressure ; Kirkwoodg K factors ; liquid association ; methanol ; n-propanol
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Precise static dielectric constants are reported for methanol, ethanol, andn-propanol at 10,25, and 40° C and at pressures up to 3 kbar. The measurements were carried out by a low-frequency bridge method using a threeterminal, all-glass cell. An uncertainty of 0.05% is claimed for the data. The results are compared to data from previous investigations, whith the agreement in the absolute magnitude poor but the agreement in the pressure coefficient reasonable in most cases. The data are analyzed in terms of the Kirkwood correlation factorg K as obtained from the Fröhlich equation. In all cases, theg K factor decreases with increased pressure. The problems involved in calculating this factor from the experimental data are discussed, and it is shown that the trends ing K are very dependent upon the assumptions made in isolating the liquid dipole moment from its gas-phase value. This fact also indicates that an interpretation of theg K values in terms of stepwise association of correlation dipoles is premature at this time.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Springer
    Journal of solution chemistry 4 (1975), S. 745-762 
    ISSN: 1572-8927
    Keywords: KCl ; KBr ; KClO3 ; KBrO3 ; KlO3 ; KClO4 ; KlO4 ; D2O ; conductance ; transference numbers ; aqueous solutions ; structural effects ; solvent isotope effects
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Precise limiting ionic conductance data are reported for the first time for the alkali metal and tetraalkylammonium ions in D2O at 10°C as well as similar data for the halate and perhalate ions in D2O and H2O at 10 and 25°C. Precise transference numbers by the moving-boundary method are also reported for KBr in D2O at 10°C and, as a check on earlier work, for KCl in D2O at 25°C. In general, the structural properties of the ions, as reflected in the temperature coefficient of the limiting ionic conductances, are enhanced in D2O compared to H2O, although the differences are often small.
    Type of Medium: Electronic Resource
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  • 4
    ISSN: 1572-8927
    Keywords: Hydrochloric acid ; water-dioxane ; water-tetrahydrofuran ; water-dimethoxyethane ; conductance ; EMF ; association constants ; short range non-coulombic interactions
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract Available emf data for HCl in water-dioxane, water-tetrahydrofuran, and water-dimethoxyethane at 25°C have been analyzed using models based on similar levels of approximation as was used previously for conductance data. The emf data were evaluated in terms of standard cell potentials, apparent distances of closest approach, association constants and a Gibbs energy term attributed to non-coulombic ion-solvent interaction. Although emf and conductance data give essentially the same results it is clear that the conductance method, with its much greater precision, is superior for this type of analysis.
    Type of Medium: Electronic Resource
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