Issue 3, 1982

Mutual diffusion coefficients of SrCl2–H2O and CsCl—H2O at 25 °C from Rayleigh interferometry

Abstract

The volume-fixed mutual diffusion coefficients of SrCl2–H2O and CsCl–H2O have been measured from dilute solution to near saturation to an accuracy of 0.1–0.2% at 25 °C, using free-diffusion Rayleigh interferometry. A few diffusion coefficients were also measured for NaCl—H2O, as were the densities of SrCl2–H2O. These new data are compared with other available diffusion and density data for these salts. Diffusion coefficients are now available for most of the aqueous alkali-metal and alkaline-earth chlorides. The effects of cation size and ionic hydration on diffusion coefficients are discussed for these two series. The mutual diffusion coefficients of the alkaline-earth chlorides have crossovers as a function of the molarity, as do those of 2–2 sulphates. In contrast, their thermodynamic diffusion coefficients not only have no crossovers, but reduce the differences between weak and strong electrolytes.

Article information

Article type
Paper

J. Chem. Soc., Faraday Trans. 1, 1982,78, 887-896

Mutual diffusion coefficients of SrCl2–H2O and CsCl—H2O at 25 °C from Rayleigh interferometry

J. A. Rard and D. G. Miller, J. Chem. Soc., Faraday Trans. 1, 1982, 78, 887 DOI: 10.1039/F19827800887

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