21 research outputs found
High temperature measurements and condensed matter analysis of the thermo-physical properties of ThO2
Values are presented for thermal conductivity, specific heat, spectral and total hemispherical emissivity of ThO2 (a potential nuclear fuel material) in a temperature range representative of a nuclear accident - 2000 K to 3050 K. For the first time direct measurements of thermal conductivity have been carried out on ThO2 at such high temperatures, clearly showing the property does not decrease above 2000 K. This could be understood in terms of an electronic contribution (arising from defect induced donor/acceptor states) compensating the degradation of lattice thermal conductivity. The increase in total hemispherical emissivity and visible/near-infrared spectral emissivity is consistent with the formation of donor/acceptor states in the band gap of ThO2. The electronic population of these defect states increases with temperature and hence more incoming photons (in the visible and near-infrared wavelength range) can be absorbed. A solid state physics model is used to interpret the experimental results. Specific heat and thermal expansion coefficient increase at high temperatures due to the formation of defects, in particular oxygen Frenkel pairs. Prior to melting a gradual increase to a maximum value is predicted in both properties. These maxima mark the onset of saturation of oxygen interstitial sites
Innovative preparation route for uranium carbide using citric acid as a carbon source
The preparation of uranium carbide (UC) by carbothermal reduction and its sintering into dense pellets by conventional means require high temperatures for long periods. We have developed a preparation route yielding fine UC powder with significantly increased sinterability. At first, a mixture of nanocrystalline UO2 embedded in amorphous carbon (nano-UO2/C) was obtained by thermal decomposition of a gel containing solubilised uranyl nitrate and citric acid. Later, the nano-UO2/C powder was treated in a conventional furnace or in a modified spark plasma sintering facility at elevated temperatures (≥1200°C) in order to obtain uranium carbide powder. The effects of initial composition, temperature, gas/vacuum atmosphere and the overall reaction kinetics are reported
Characterization of prototypic UO2-ZrO2 debris after steam explosion experiments in the KROTOS facility
Sub-micrometre grained UO 2 pellets consolidated from sol gel beads using spark plasma sintering (SPS)
Electron Microscopy Analyses of Samples Devoted to the Study of the Nuclear Reactor Severe Accident
Spark plasma sintering of fine uranium carbide powder
Results of uranium carbide sintering using a spark plasma sintering facility are presented here. The
initial uranium carbide powder is produced from the thermal decomposition of a citric acid and uranium
nitrate mixture. The study shows that spark plasma sintering is a very efficient compaction tool for
uranium carbide material. Both onset of sintering and final density are strongly correlated to the UC synthesis
conditions
Thermally-insulated ultra-fast high temperature sintering (UHS) of zirconia: A master sintering curve analysis
Ultrahigh Temperature Flash Sintering of Binder-Less Tungsten Carbide within 6 s
We report on an ultrarapid (6 s) consolidation of binder-less WC using a novel Ultrahigh temperature Flash Sintering (UFS) approach. The UFS technique bridges the gap between electric resistance sintering (≪1 s) and flash spark plasma sintering (20–60 s). Compared to the well-established spark plasma sintering, the proposed approach results in improved energy efficiency with massive energy and time savings while maintaining a comparable relative density (94.6%) and Vickers hardness of 2124 HV. The novelty of this work relies on (i) multiple steps current discharge profile to suit the rapid change of electrical conductivity experienced by the sintering powder, (ii) upgraded low thermal inertia CFC dies and (iii) ultra-high consolidation temperature approaching 2750 °C. Compared to SPS process, the UFS process is highly energy efficient (≈200 times faster and it consumes ≈95% less energy) and it holds the promise of energy efficient and ultrafast consolidation of several conductive refractory compounds