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The article contains sections titled: 1. Introduction 2. History 3. Physical Properties 3.1. Radioactivity 3.2. Modifications 3.3. Mechanical Properties 3.4. Thermal Properties 3.5. Electrical and Electrochemical Properties 3.6. Magnetic Properties 4. Chemical Properties 5. Occurrence, Requirement, and Production Figures 5.1. Occurrence 5.2. Resources, Requirement, and Production Figures 6. Production 6.1. Uses of Uranium and Uranium Compounds 6.2. From Ore to End Product‐A Review of Processes 6.2.1. From Crude Ore to Yellow Cake 6.2.2. From Yellow Cake to UF 6 6.2.3. From UF 6 to the Nuclear Fuel UO 2 6.3. Detailed Description of the Processes 6.3.1. Digestion and Leaching of Ores 6.3.1.1. Acidic Ores 6.3.1.2. Alkaline Ores 6.3.1.3. Digestion of Phosphate Rock 6.3.2. Treatment of the Liquor 6.3.2.1. Uranium Recovery by Ion Exchange 6.3.2.2. Uranium Recovery by Solvent Extraction 6.3.2.3. Eluex Process 6.3.3. Production of Uranium Ore Concentrate 6.3.3.1. From Precipitation to Yellow Cake Production 6.3.3.2. Processing of Phosphate Liquor and Precipitation of AUC 6.3.4. Final Purification of Uranium Concentrate 6.3.4.1. Dissolution of Yellow Cake 6.3.4.2. Extractive Purification 6.3.5. Production of UO 3 and UO 2 from Purified Uranyl Nitrate Solution 6.3.5.1. Evaporation of Uranyl Nitrate Solution and Denitration by Thermal Decomposition 6.3.5.2. Precipitation of Uranium by the ADU and AUC Processes 6.3.5.3. Reduction of Precipitated Product to UO 2 Powder 6.3.6. Production of UF 4 6.3.6.1. Hydrofluorination of UO 2 6.3.6.2. Hydration and Hydrofluorination of UO 3 6.3.7. Production of UF 6 from UF 4 6.3.7.1. Process Description 6.3.7.2. Chemical Reactors 6.3.7.3. Removal of Excess Fluorine from UF 6 6.3.8. Complete Plant for Production of UF 6 from Uranyl Nitrate 6.3.8.1. French Process in Pierrelatte 6.3.8.2. Allied Chemical Process 6.3.9. Enrichment of 235 U 6.3.9.1. Diffusion Process 6.3.9.2. Ultracentrifuges 6.3.9.3. Nozzle Process 6.3.9.4. Chemical Enrichment 6.3.9.5. Laser Separation Process 6.3.9.6. Plasma Processes 6.3.10. Production of UO 2 Pellets from UF 6 6.3.10.1. Conversion of UF 6 to UO 2 6.3.10.2. Possible Future Developments in the Conversion of UF 6 to UO 2 Powder 6.3.10.3. Pelletizing of UO 2 Powder 6.3.11. Production of Uranium Metal 6.3.11.1. Reduction of UF 6 to UF 4 6.3.11.2. Reduction of UF 4 to Uranium Metal 6.3.11.3. Production of Uranium Powder 7. Uranium Alloys 7.1. Classification 7.2. Production of Important Alloys 8. Uranium Compounds 8.1. Halides 8.1.1. Trivalent Halides 8.1.2. Uranium Tetrahalides 8.1.3. Uranium Pentafluoride 8.1.4. Uranium Hexafluoride 8.2. Carbides 8.3. Nitrides 8.4. Oxides 8.4.1. Uranium Dioxide 8.4.2. Uranium Trioxide 8.4.3. Triuranium Octaoxide 8.4.4. Peroxides 8.5. Nitrates, Sulfates, and the Carbonato Complex 8.5.1. Nitrates 8.5.2. Sulfates 8.5.3. Tricarbonatodioxouranate 9. Safety 9.1. Radiation Shielding 9.2. Safety Against Uncontrolled Criticality 9.3. Geometrically Safe Vessels 9.4. Apparatus with Heterogeneous Neutron Absorbers
The surface morphology characteristics of postenrichment deconversion products in the nuclear fuel cycle are important for producing nuclear fuel pellets. They also provide the first opportunity for a microstructural signature after conversion to gaseous uranium hexafluoride (UF 6 ). This work synthesizes uranium oxides from uranyl fluoride (UO 2 F 2 ) starting solutions by the wet ammonium diuranate route and a modification of the dry route. Products are reduced under a nitrogen/hydrogen atmosphere, with and without water vapor in the reducing environment. The crystal structures of the starting materials and resulting uranium oxides are characterized by powder X-ray diffraction. Scanning electron microscopy (SEM) and focused ion beam SEM with energy-dispersive X-ray spectroscopy (EDX) are used to investigate microstructural properties and quantify fluorine impurity concentrations. Heterogeneous distributions of fluorine with unique morphology characteristics were identified by backscatter electron imaging and EDX; these regions had elevated concentrations of fluorine impurities relating to the incomplete reduction of UO 2 F 2 to UO 2 and may provide a novel nuclear forensics morphology signature for nuclear fuel and U metal precursors.
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