In the context of a comprehensive campaign for the characterisation of transmutation fuels for next generation nuclear reactors, the melting behaviour of mixed uranium-americium dioxides has been experimentally studied for the first time by laser heating, for Am concentrations up to 70 mol. % under different types of atmospheres. Extensive post-melting material characterisations were then performed by X-ray absorption spectroscopy and electron microscopy. The melting temperatures observed for the various compositions follow a markedly different trend depending on the experimental atmosphere. Uranium-rich samples melt at temperatures significantly lower (around 2700 K) when they are laser-heated in a strongly oxidizing atmosphere compressed air at (0.300 ± 0.005) MPa, compared to the melting points (beyond 3000 K) registered for the same compositions in an inert environment (pressurised Ar). This behaviour has been interpreted on the basis of the strong oxidation of such samples in air, leading to lower-melting temperatures. Thus, the melting temperature trend observed in air is characterized, in the purely pseudo-binary dioxide plane, by an apparent maximum melting temperature around 2850 K for 0.3 < x(AmO₂) < 0.5. The melting points measured under inert atmosphere uniformly decrease with increasing americium content, displaying an approximately ideal solution behaviour if a melting point around 2386 K is assumed for pure AmO₂. In reality, it will be shown that the (U, Am)-oxide system can only be rigorously described in the ternary U-Am-O phase diagram, rather than the UO₂-AmO₂ pseudo-binary, due to the aforementioned over-oxidation effect in air. Indeed, general departures from the oxygen stoichiometry (Oxygen/Metal ratios ≠ 2.0) have been highlighted by the X-ray Absorption Spectroscopy (XAS). Finally, to help interpret the experimental results, thermodynamic computations based on the CALPHAD method will be presented.

The formation of a thin layer, the so-called Joint Oxyde-Gaine (JOG), between the (U,Pu)O2 fuel pellets and the cladding has been observed in fast neutron reactors, due to the accumulation of volatile fission products. Cs2MoO4 is known to be one of the major components of the JOG, but other elements are also present, in particular tellurium and palladium. In this work, an investigation of the structural and thermodynamic properties of Cs2TeO4 and Cs2Mo1-xTexO4 solid solution is reported. The existence of a complete solubility between Cs2MoO4 and Cs2TeO4 is demonstrated, combining X-ray diffraction (XRD), neutron diffraction (ND), and X-ray absorption spectroscopy (XAS) results. High-temperature XRD measurements were moreover performed on Cs2TeO4, which revealed the existence of a α-β phase transition around 712 K. Thermal expansion coefficients were also obtained from these data. Finally, phase equilibra points in the Cs2MoO4-Cs2TeO4 pseudobinary phase diagram were collected using differential scanning calorimetry and used to develop a thermodynamic model for this system using a regular solution formalism.

Neutron diffraction, X-ray absorption spectroscopy (XAS), and Raman spectroscopy measurements of the quaternary perovskite phase Ba₂NaMoO_5.5 have been performed in this work. The cubic crystal structure in space group Fm3&macr; m has been refined using the Rietveld method. X-ray absorption near-edge structure spectroscopy (XANES) measurements at the Mo K-edge have confirmed the hexavalent state of molybdenum. The local structure of the molybdenum octahedra has been studied in detail using extended X-ray absorption fine structure (EXAFS) spectroscopy. The Mo-O and Mo-Ba distances have been compared to the neutron diffraction data with good agreement. The coefficient of thermal expansion measured in the temperature range of 303-923 K, using high temperature X-ray diffraction (HT-XRD) (α_V = 55.8 × 10^-6 K), has been determined to be ∼2 times higher than that of the barium molybdates BaMoO₃ and BaMoO₄. Moreover, no phase transition nor melting have been observed, neither by HT-XRD nor Raman spectroscopy nor differential scanning calorimetry, up to 1473 K. Furthermore, the standard enthalpy of formation (Δ_fH_m°) for Ba₂NaMoO_5.5(cr) has been determined to be -(2524.75 ± 4.15) kJ mol^-1 at 298.15 K, using solution calorimetry. Finally, the margin for safe operation of sodium-cooled fast reactors (SFRs) has been assessed by calculating the threshold oxygen potential needed, in liquid sodium, to form the quaternary compound, following an interaction between irradiated mixed oxide (U,Pu)O₂ fuel and sodium coolant.

To assure the safety of oxide-fuel based nuclear reactors, the knowledge of the atomic-scale properties of U_1−yM_yO_2±x materials is essential. These compounds show complex chemical properties, originating from the fact that actinides and rare earths may occur with different oxidation states. In these mostly ionic materials, aliovalent cationic configurations can induce changes in the oxygen stoichiometry, with dramatic effects on the properties of the fuel. First studies on U_1−yAm_yO_2±x indicated that these materials exhibit particularly complex electronic and local-structure configurations. Here we present an in-depth study of these compounds, over a wide compositional domain, by combining XRD, XAS and Raman spectroscopy. We provide evidences of the co-existence of four different cations (U⁴⁺, U⁵⁺, Am³⁺, Am⁴⁺) in U_1−yM_yO_2±x compounds, which nevertheless maintain the fluorite structure. Indeed, we show that the cationic sublattice is basically unaffected by the extreme multi-valence states, whereas complex defects are present in the oxygen sublattice.

The development at the Delft University of Technology (TU Delft, The Netherlands) of an experimental set-up dedicated to high-temperature in situ EXAFS measurements of radioactive, air-sensitive and corrosive fluoride salts is reported. A detailed description of the sample containment cell, of the furnace design, and of the measurement geometry allowing simultaneous transmission and fluorescence measurements is given herein. The performance of the equipment is tested with the room-temperature measurement of thorium tetrafluoride, and the Th—F and Th—Th bond distances obtained by fitting of the EXAFS data are compared with the ones extracted from a refinement of neutron diffraction data collected at the PEARL beamline at TU Delft. The adequacy of the sample confinement is checked with a mapping of the thorium concentration profile of molten salt material. Finally, a few selected salt mixtures (LiF:ThF₄) = (0.9:0.1), (0.75:0.25), (0.5:0.5) and (NaF:ThF₄) = (0.67:0.33), (0.5:0.5) are measured in the molten state. Qualitative trends along the series are discussed, and the experimental data for the (LiF:ThF₄) = (0.5:0.5) composition are compared with the EXAFS spectrum generated from molecular dynamics simulations.

The physicochemical properties of the potassium neptunate K₂NpO₄ have been investigated in this work using X-ray diffraction, X-ray absorption near edge structure (XANES) spectroscopy at the Np-L₃ edge, and low-temperature heat capacity measurements. A Rietveld refinement of the crystal structure is reported for the first time. The Np(VI) valence state has been confirmed by the XANES data, and the absorption edge threshold of the XANES spectrum has been correlated to the Mössbauer isomer shift value reported in the literature. The standard entropy and heat capacity of K₂NpO₄ have been derived at 298.15 K from the low-temperature heat capacity data. The latter suggest the existence of a magnetic ordering transition around 25.9 K, most probably of the ferromagnetic type.

The electronic structure of U^V- and U^VI-containing uranates NaUO₃and Pb₃UO₆was studied by using an advanced technique, namely X-ray absorption spectroscopy (XAS) in high-energy-resolution fluorescence-detection (HERFD) mode. Due to a significant reduction in core–hole lifetime broadening, the crystal-field splittings of the 5f shell were probed directly in HERFD-XAS spectra collected at the U 3d edge, which is not possible by using conventional XAS. In addition, the charge-transfer satellites that result from U 5f–O 2p hybridization were clearly resolved. The crystal-field parameters, 5f occupancy, and degree of covalency of the chemical bonding in these uranates were estimated by using the Anderson impurity model by calculating the U 3d HERFD-XAS, conventional XAS, core-to-core (U 4f–3d transitions) resonant inelastic X-ray scattering (RIXS), and U 4f X-ray photoelectron spectra. The crystal field was found to be strong in these systems and the 5f occupancy was determined to be 1.32 and 0.84 electrons in the ground state for NaUO₃and Pb₃UO₆, respectively, which indicates a significant covalent character for these compounds.