The optimized Gibbs energies for the second-nearest neighbours exchange reactions of the liquid solution were not reported correctly in Eqs. (17)–(19) in our recent work [1]. The corresponding equations should read: [Formula presented] [Formula presented] [Formula presented]@en

The structural, thermochemical, and thermophysical properties of the NaF-ThF4 fuel system were studied with experimental methods and molecular dynamics (MD) simulations. Equilibrium MD (EMD) simulations using the polarizable ion model were performed to calculate the density, molar volume, thermal expansion, mixing enthalpy, heat capacity, and distribution of [ThFn]m- complexes in the (Na,Th)Fx melt over the full concentration range at various temperatures. The phase equilibria in the 10-50 mol % ThF4 and 85-95 mol % ThF4 regions of the NaF-ThF4 phase diagram were measured using differential scanning calorimetry, as were the mixing enthalpies at 1266 K of (NaF/ThF4) = (0.8:0.2), (0.7:0.3) mixtures. Furthermore, the β-Na2ThF6 and NaTh2F9 compounds were synthesized and subsequently analyzed with the use of X-ray diffraction. The heat capacities of both compounds were measured in the temperature ranges (2-271 K) and (2-294 K), respectively, by thermal relaxation calorimetry. Finally, a CALPHAD model coupling the structural and thermodynamic data was developed using both EMD and experimental data as input and a quasichemical formalism in the quadruplet approximation. Here, 7- and 8-coordinated Th4+ cations were introduced on the cationic sublattice alongside a 13-coordinated dimeric species to reproduce the chemical speciation, as calculated by EMD simulations and to provide a physical description of the melt.@en

The short-range structures of LiF-ThF4, NaF-AnF4, KF-AnF4, and Cs-AnF4 (An = Th, U), were probed using in situ high temperature Extended X-ray Absorption Fine Structure (EXAFS) spectroscopy. Signally, the EXAFS spectra of pure molten ThF4 and UF4 were measured for the first time. The data were interpreted with the aid of Molecular Dynamics (MD) and standard fitting of the EXAFS equation. As in related studies, a speciation distribution dominated by [AnFx]4-x (x = 7, 8, 9) coordination complexes was observed. The average coordination number was found to decrease with the increasing size of the alkali cation, and increase with AnF4 content. An average coordination number close to 6, which had not been detected before in melts of alkali actinide fluorides, was seen when CsF was used as solvent. This journal is @en

© 2021 The Authors LiF-UF4 is a key binary system for molten fluoride reactor technology, which has not been scrutinized as thoroughly as the closely related LiF-ThF4 system. The phase diagram equilibria in the system LiF-UF4 are explored in this work with X-ray diffraction (XRD) and differential scanning calorimetry (DSC). The short-range ordering in the molten salt solution is moreover surveyed with Extended X-ray Absorption Fine Structure spectroscopy (EXAFS) and interpreted using a combination of standard fitting of the EXAFS data and Molecular Dynamics (MD) simulations with a Polarizable Ion Model (PIM) potential. The density, excess molar volume, thermal expansion, heat capacity, and enthalpy of mixing are extracted from the MD simulations across a range of temperatures and compositions; the behavior is non-ideal, with reasonably good agreement with the experimental data. Also calculated is the distribution of heteropolyanions in the liquid solution, and modelled using the quasi-chemical formalism in the quadruplet approximation taking into account the existence of the single-shell complexes [UF7]3−, [UF8]4−, and the dimeric species [U2F14]6−. Subjecting the optimization of the excess Gibbs energy parameters of the liquid solution to the constraints of the phase diagram data and local structure of the melt as derived from the EXAFS and coupled MD simulations, a CALPHAD-type assessment is proposed, linking structural and thermodynamic properties, with a rigorous physical description of the melt.@en

The (Li,Be)Fx fluoride salt is an ionic liquid with complex non-ideal thermodynamic behaviour due to the formation of short-range order. In this work, we explore the relationship between local structure, thermo-physical and thermodynamic properties in this system using a multidisciplinary approach that couples molecular dynamics simulations using the Polarizable Ion Model (PIM) and thermodynamic modelling assessment using the CALPHAD method. The density, thermal expansion, viscosity, thermal conductivity, molar and mixing enthalpies and heat capacity of the (Li,Be)Fx melt are extracted from the polarizable ionic interaction potentials and investigated across a wide range of compositions and temperatures. The agreement with the available experimental data is generally very good. The local structure is also examined in detail, in particular the transition between a molecular liquid with Li+, BeF4 2− and F− predominant species at low BeF2 content, and a polymeric liquid at high BeF2 content, with the formation of polymers (Be2F7 3−, Be3F10 4−, Be4F13 5−, etc.), and finally of a three-dimensional network of corner-sharing tetrahedrally coordinated Be2+ cations for pure BeF2. Based on the available experimental information and the output of the MD simulations, we moreover develop for the first time a coupled structural-thermodynamic model for the LiF-BeF2 system based on the quasi-chemical formalism in the quadruplet approximation, that provides a physical description of the melt and reproduces (in addition to the thermodynamic data) the chemical speciation of beryllium polymeric species predicted from the simulations.@en