Metallurgical grade alumina is produced worldwide through the well-known Bayer process, which unavoidably generates bauxite residue (BR, also known as red mud) in almost equal amounts to alumina. This study aims the valorization of BR through a smelting-reduction process to obtain calcium aluminate slags that can be a proper feed for alumina recovery via the Pedersen process. It investigates the thermodynamics and characteristics of the slags and pig iron produced from mixtures of BR, a bauxite beneficiation byproduct, and lime. In this context, the evolution of the different phases in the slags is studied with advanced analytical techniques and thermodynamic calculations. According to the results, a CaO/Al2O3 mass ratio within 1.3 to 1.4 in the slags can yield more Al2O3-containing leachable phases, such as CaO·Al2O3 and 12CaO·7Al2O3. The cooling dictates the amount and the characteristics of these phases, and the slower cooling rate yields improved slag characteristics. The distribution of the elements between the slag and metal phases shows that iron is separated, and the majority of the P, Cr, Ni, and V are distributed in the produced pig iron, while S, Ti, and Si are mostly concentrated in the slags.
The metallurgical structure of an ingot produced by vacuum arc remelting ( VAR) depends critically on the temperature distribution within the liquid portion of the partially solidified ingot. This, in turn, depends on the fluid motion in the pool, since the dominant mechanism for transporting heat is convection. There are three primary sources of motion: buoyancy; Lorentz forces arising from the passage of current through the pool; and Lorentz forces arising from the presence of external inductors. These forces are constantly in competition with each other, and each tends to induce a quite different distribution of velocity and temperature. We examine the transition between these different flow regimes and derive dimensionless criteria which determine which regime is dominant. We show that the structure of an ingot produced by VAR depends critically on the temperature distribution within the liquid portion of the partially solidified ingot. This, in turn, depends on the fluid motion in the pool, since the dominant mechanism for transporting heat is convection. There are three primary sources of motion: buoyancy; Lorentz forces arising from the passage of current through the pool; and Lorentz forces arising from the presence of external inductors. These forces are constantly in competition with each other, and each tends to induce a quite different distribution of velocity and temperature. We examine the transition between these different flow regimes and derive dimensionless criteria which determine which regime is dominant. We show that modest changes in ingot current can produce radical changes in temperature distribution, and that weak, steady magnetic fields, of only ~1 Gs, can induce a powerful swirling motion which suppresses the normal flow.MST/4376
A high temperature process for recycling spent nickel-metal hydride rechargeable batteries has been recently developed at SINTEF/NTNU. The spent battery modules were first frozen with liquid nitrogen for the de-activation and brittle fracture treatment. The broken steel scraps and plastics were then separated by the mechanical classification and magnetic separation. The remaining positive and negative electrodes, together with the polymer separator, were heated to 600-800oC in order to remove the organic components and further separate the Ni-based negative electrode. XRF analyses indicate that the heat-treated materials consist mainly of nickel, rare earth and cobalt oxides. The valuable rare earth oxides were further recovered by the high-temperature slagging treatment. The waste metallurgical slags, consist mainly of SiO2 and CaO, were used as the rare earth oxide absorbent. After the high temperature slagging treatment, over 98% of nickel and cobalt oxides were reduced to the metal phase; meanwhile almost all rare earth oxides remain in the molten slags. Furthermore, EPMA and XRF analyses of the slag samples indicate that the rare earth oxides selectively precipitate in the forms of solid xSiO2•yCaO•zRe2O3. The matrix of slag phase is Re2O3 deficient, typically being less than 5 wt%. This provides a sound basis to further develop the high-temperature process of concentrating the Re2O3 oxides in slags
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