Solvent isotope effect on ion mobility in water at high pressure. Conductance and transference number of potassium chloride in compressed heavy water

التفاصيل البيبلوغرافية
العنوان: Solvent isotope effect on ion mobility in water at high pressure. Conductance and transference number of potassium chloride in compressed heavy water
المؤلفون: K. Shimizu, M. Nakahara, M. Ueno, M. Zenke
المصدر: The Journal of Chemical Physics. 83:280-287
بيانات النشر: AIP Publishing, 1985.
سنة النشر: 1985
مصطلحات موضوعية: Heavy water, Chemistry, Inorganic chemistry, Analytical chemistry, General Physics and Astronomy, Conductance, Dielectric, Volume viscosity, Ion, Solvent, chemistry.chemical_compound, Kinetic isotope effect, Ionic conductivity, Physical and Theoretical Chemistry
الوصف: Limiting molar conductances of the K+ and Cl− ions in heavy and light water have been determined at 25 °C as a function of pressure up to 2 kbar from the measured conductances and transference numbers of KCl. The residual friction coefficients (Δζ) are obtained for the cation and the anion in D2O and H2O by using the determined limiting conductance and the bulk viscosity of solvent and compared with the corresponding values predicted by applying the Hubbard–Onsager (HO) dielectric friction theory at various pressures below 1 kbar. At atmospheric and high pressures Δζ of the K+ ion in D2O is larger than that in H2O just as predicted by the HO theory, but Δζ of the Cl− ion in D2O is smaller than that in H2O on the contrary to the theoretical prediction. The reverse solvent isotope effect on Δζ(Cl−) suggests that a microscopic viscosity in the vicinity of the relatively large ion is smaller than the bulk viscosity used in the continuum theory.
تدمد: 1089-7690
0021-9606
DOI: 10.1063/1.449821
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::847012bc5a599b5c12686c2e44323f43
https://doi.org/10.1063/1.449821
رقم الانضمام: edsair.doi...........847012bc5a599b5c12686c2e44323f43
قاعدة البيانات: OpenAIRE
الوصف
تدمد:10897690
00219606
DOI:10.1063/1.449821