Experimental investigation and thermodynamic assessment of the BaCl2–CeCl3 system
D.C. Alders (TU Delft - RST/Reactor Physics and Nuclear Materials)
John Vlieland (TU Delft - RST/Technici Pool)
M. Thijs (TU Delft - RID/TS/Technici Pool)
R. J.M. Konings (TU Delft - RST/Reactor Physics and Nuclear Materials)
A.L. Smith (TU Delft - RST/Reactor Physics and Nuclear Materials)
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Abstract
The thermodynamic and thermo-physical properties of the molten salt system [Formula presented] have been investigated using an experimental and modelling approach. This molten salt system includes a single intermediate compound [Formula presented], whose structure has been investigated using X-ray and neutron diffraction. Furthermore, this system exhibits solubility of [Formula presented] in [Formula presented] at high temperatures up to a concentration of around 25% [Formula presented] at 1060 K. Additionally, our measurements show solubility of [Formula presented] in [Formula presented] up to about 5% [Formula presented] at 973 K. The investigation of these solid solutions has been performed using quenching experiments and subsequent post-characterisation by X-ray diffraction (XRD). Phase diagram equilibria have also been investigated using differential scanning calorimetry (DSC). Using the aforementioned information on phase transitions, intermediate compound formation, and mutual solid solubility, a thermodynamic assessment of the system has been performed using the CALPHAD method. The model for the Gibbs energy of the liquid solution is the quasi-chemical formalism in the quadruplet approximation, while the model for the Gibbs energy of the solid solutions is a two-sublattice polynomial model.