Calculation of the thermodynamic and transport properties of aqueous species at high pressures and temperatures: Aqueous tracer diffusion coefficients of ions to 1000°C and 5 kb

1988 ◽  
Vol 52 (1) ◽  
pp. 63-85 ◽  
Author(s):  
Eric H. Oelkers ◽  
Harold C. Helgeson
2017 ◽  
Vol 19 (16) ◽  
pp. 10527-10542 ◽  
Author(s):  
Thomas Rüther ◽  
Mitsuhiro Kanakubo ◽  
Adam S. Best ◽  
Kenneth R. Harris

All three ion–ion interactions contribute to transport properties in {Li[FSI]–[Pyr13][FSI]} mixtures. Tracer diffusion coefficients of LI+ in [Pyr13][FSI] are predicted.


1970 ◽  
Vol 25 (12) ◽  
pp. 1921-1925 ◽  
Author(s):  
Ante Bengtzelius ◽  
Ann-Mari Josefson ◽  
Arnold Kvist ◽  
Kjell Schroeder

Abstract The phase diagram and electrical conductivity of cubic lithium sulphate with small quantities of thulium sulphate and aluminium sulphate have been measured. We have also measured the tracer diffusion coefficients of Tm3+ and Al3+ in pure cubic lithium sulphate. The diffusion coefficients of the trivalent ions are much lower than those of the univalent and divalent cations. The results indicate that the trivalent ions are trapped in the lattice.


1994 ◽  
Vol 369 ◽  
Author(s):  
Sanjeev Aggarwal ◽  
Rudiger Dieckmann

AbstractCation diffusion in the spinel solid solution (Fe1-xTix)3-δO4 (0≤ x ≤ 0.3) was investigated at 1200 ºC as a function of oxygen activity, aO2 and cationic composition, x. At different cationic compositions, cation tracer diffusion coefficients, D*Me of Me = Fe and Ti were measured as a function of oxygen activity. Plots of log DMe vs. loga0 show V-shaped curves, indicating that different types of point defects prevail at high anc low oxygen activities. Thermogravimetric experiments were conducted, using a high resolution microbalance, to determine the deviation from stoichiometry in (Fe1-xTix)3-δO4 at 1200 °C. δversus log aO2 curves are S-shaped. An analysis of the oxygen activity dependences of thecation diffusion coefficients and the deviation from stoichiometry with regardto the point defect structure suggests that at high oxygen activities cation vacancies are the predominant defects governing the deviation from stoichiometry and the diffusion ofcations. At low oxygen activities, and at small values of x, cation interstitials determine the deviation from stoichiometry, while they dominate for 0 ≤ x ≤ 0.3 inthe cation diffusion.


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