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The rare earth elements (REEs) comprise a set of 17 chemical elements in the periodic table, specifically the 15 lanthanides plus scandium and yttrium. REEs and alloys that contain them are used in devices such as computer memory, rechargeable batteries, cell phones, catalytic converters, magnets, fluorescent lighting, and many more (Krishnamurthy and Gupta, 2004). China supplies about 94% of the REE demand, with the remaining 6% coming from Russia and Estonia, the USA, India, Malaysia, and Brazil (Zhanheng, 2011). Increased industrial development in China has prompted the Chinese government to limit annual export quotas to approximately 35 kt of rare earth oxides (REOs), while non-Chinese annual demand is expected to reach 80 kt by the year 2015. This constriction of supply is being met by the development of many new rare earth mining projects, each of which has its own unique mining and processing
The rare earth elements (REEs) comprise a set of 17 chemical elements in the periodic table, specifically the 15 lanthanides plus scandium and yttrium. REEs and alloys that contain them are used in devices such as computer memory, rechargeable batteries, cell phones, catalytic converters, magnets, fluorescent lighting, and many more (Krishnamurthy and Gupta, 2004). China supplies about 94% of the REE demand, with the remaining 6% coming from Russia and Estonia, the USA, India, Malaysia, and Brazil (Zhanheng, 2011). Increased industrial development in China has prompted the Chinese government to limit annual export quotas to approximately 35 kt of rare earth oxides (REOs), while non-Chinese annual demand is expected to reach 80 kt by the year 2015. This constriction of supply is being met by the development of many new rare earth mining projects, each of which has its own unique mining and processing
The article contains sections titled: 1. Introduction 2. Mineralogy, Abundance, Occurrence 3. Properties 3.1. Properties of the Nuclei 3.2. Properties of the Atoms and Ions 3.2.1. Electronic Configuration, Position in the Periodic Table 3.2.2. Oxidation States, Atomic and Ionic Radii 3.2.3. Magnetic and Spectral Properties 3.2.4. Bonding, Coordination Numbers 3.3. Other Chemical and Physical Properties 3.3.1. Reactivity 3.3.2. Crystal Structures 3.3.3. Melting and Boiling Points 3.3.4. Elastic Properties 3.4. Miscibility and Alloying Behavior 3.5. Mechanical Workability 4. Digestion of Rare Earth Ores 4.1. Wet Chemical Digestion 4.1.1. Monazite 4.1.2. Bastnaesite 4.1.3. Other Ores 4.2. Direct Chlorination at High Temperature 5. Rare‐Earth Separation 5.1. Principles of Separation 5.2. Separation by Classical Methods 5.2.1. Fractional Crystallization 5.2.2. Fractional Precipitation 5.2.3. Separations Based on Oxidation State Changes 5.3. Separation by Ion Exchange 5.3.1. Ion Exchange with Chelating Agents 5.3.2. Separation Process 5.3.3. Industrial Processes 5.3.4. Disadvantages of Ion Exchange 5.3.5. Molecular Recognition Processes 5.4. Separation by Liquid‐Liquid Extraction 5.4.1. Theoretical Basis 5.4.1.1. Distribution Coefficient and Separation Factor 5.4.1.2. Method of Operation 5.4.2. Extractants 5.4.2.1. Neutral Extractants 5.4.2.2. Acidic Extractants 5.4.2.3. Amines and Quaternary Ammonium Salts as Extractants 5.4.2.4. Synergistic Effects 5.4.2.5. Ionic Liquids 5.4.3. Industrial Liquid–Liquid Extraction 5.4.3.1. Separation of Europium and Yttrium Oxides 5.4.3.2. Separation of Scandium 6. Production of the Metals 6.1. Fused‐Salt Electrolysis 6.2. Metallothermic Reduction 6.3. Purification 7. Analysis 8. Compounds 8.1. Hydrides 8.2. Oxides, Hydroxides, Peroxides, Salts of Inorganic Oxoacids, Double Salts 8.3. Halides 8.3.1. Trivalent Halides 8.3.2. Tetravalent Halides 8.3.3. Divalent Halides 8.3.4. Monovalent Halides 8.4. Chalcogenides 8.5. Nitrides 8.6. Carbides 8.7. Coordination Compounds with Organic Ligands 8.8. Organometallic Compounds 9. Uses 9.1. Industrial Periods 9.2. Metallurgy 9.2.1. Metals 9.2.2. Alloys and Intermetallic Compounds 9.3. Catalysts 9.3.1. Fluidified Cracking Catalysts 9.3.2. Automotive Catalysts 9.3.3. Production of Organic Compounds 9.4. Glass and Ceramic Industry 9.5. Electronics 9.6. Magnets 9.7. Photonics 9.7.1. Lasers 9.7.2. Telecommunications 9.7.3. Phosphors for Lighting and Displays 9.7.4. Security and Identification Tags, Signage, and Structural Health Sensors 9.7.4.1. Downshifting Tags 9.7.4.2. Upconversion Tags 9.7.4.3. Persistent‐Luminescence Phosphors 9.7.4.4. Mechanoluminescent Detectors 9.7.4.5. Scintillators 9.7.5. Luminescent Thermometers 9.8. Energy‐Related Applications 9.8.1. Fuel Cells 9.8.2. Photovoltaic Processes 9.8.3. Luminescent Solar Concentrators and Solar Cells 9.8.4. Magnetic and Optical Cooling 9.8.5. Other Applications 9.9. Medical Applications 9.10. Miscellaneous Applications 10. Economic Aspects 11. Toxicology
The Young's modulus for a series of binary Mg–Gd and Mg–Nd alloys are studied in the present work. Fine and homogeneous grain structures are prepared by using hot extrusion. The results demonstrate that the Young's modulus of Mg–Gd alloys increase linearly by the increase of Gd in solid solution. Aging treatments are applied to the Mg–0.79–2.43 at% Gd alloys. A needle‐like orthorhombic structure β′ phase is formed in Mg matrix. Due to a higher Young's modulus of the intermetallic β′ phase which is estimated to be 80 GPa, the Young's modulus of Mg–Gd alloys are enhanced by aging. The results for Mg–Nd alloys indicate that Young's modulus firstly decreases and reaches 42.53 GPa for Mg–0.18 at% Nd which is attributed to the solid solution of Nd in Mg. The Mg41Nd5 particles appear in Mg matrix when Nd content is higher than 0.18 at%, and Young's modulus of the particles is tested as 57.0 GPa. Thus, the Young's modulus increases to 43.42 GPa for Mg–0.63 at% Nd. The Young's modulus of Mg alloys are affected by altering the crystal cell parameters with solid solutes, and/or the formation of precipitate phases with varying amounts.
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