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  • Articles: DFG German National Licenses  (2)
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  • Articles: DFG German National Licenses  (2)
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  • 1
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 92 (1990), S. 2548-2552 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Limiting molar conductances of the K+ and Cl− ions in heavy and light water have been determined at 45 °C as a function of pressure up to 2000 kgf cm−2 (1 kgf cm−2 =0.9807×105 Pa) from the measured conductances and transference numbers of KCl. The residual friction coefficients (Δζobs ) of the K+ and Cl− ions obtained by using their limiting molar conductances and the bulk viscosity of solvent are compared up to 1000 kgf cm−2 with the corresponding values (ΔζHO ) predicted by the Hubbard–Onsager dielectric friction theory. As predicted, Δζobs for the cation in H2 O is smaller than that in D2 O and slightly decreases with increasing pressure, while its value in D2 O is almost invariant in the pressure range studied. The failure of the continuum theory in D2 O indicates that the effect of the open structure of water on the cation migration cannot be neglected even at 45 °C because of stronger hydrogen bonds in D2 O than in H2 O. For the anion, on the other hand, the continuum theory shows more serious limitations: (i) Δζobs (Cl−) in H2 O is not smaller than that in D2 O even at 45 °C with a large difference at high pressures and (ii) Δζobs (Cl−) becomes negative in both types of water at high pressures. The difference in Δζ(Cl−) between theory and experiment at 45 °C, however, becomes much smaller than that at lower temperatures.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 4678-4683 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Limiting molar conductances of the K+ and Cl− ions in heavy and light water have been determined at 5 °C as a function of pressure up to 1500 kgf cm−2 (1 kgf cm−2=0.9807×105 Pa) from the measured conductances and transference numbers of KCl. The residual friction coefficients (Δζ) are obtained for the cation and anion in D2O and H2O by using the determined limiting conductance and the bulk viscosity of solvent, and they are compared with the corresponding values predicted by applying the Hubbard–Onsager (HO) dielectric friction theory at various pressures below 1000 kgf cm−2. At atmospheric and high pressures, the solvent isotope and temperature effects on Δζ observed for the K+ ion are qualitatively in agreement with the theoretical prediction. However, the slightly positive pressure coefficients of Δζ(K+) are obtained in both solvents at 5 °C contrary to the theoretical prediction. Furthermore, Δζ(K+) in D2O at 5 °C is smaller than the theoretical one. These results suggest that another mechanism such as the passing through cavities one plays a more important role in ion migration of the K+ ion at lower temperatures and in D2O. On the other hand, the reverse solvent isotope and temperature effects on Δζ(Cl−), and the negative values of Δζ(Cl−) are found. These anomalies cannot be explained by the continuum theory.
    Type of Medium: Electronic Resource
    Library Location Call Number Volume/Issue/Year Availability
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