The casting structure of the AA6063 alloy contains intermetallic particles of β-Al₅FeSi, which can result in the fragility of the cast pieces. However, with heat treatment, the β phase transforms from a needle or plate form into an intermetallic phase known as α, which resembles Chinese-script in its morphology. To analyze the effect of the ratio of Fe/Mn with different ratios of 0.5, 0.75, and 1, a heat treatment process is used with intermittent interruptions. The alloy is subjected to a temperature of 575 °C for 12 h to determine the microstructural evolution of the β-Al₆FeMn and α-Al₁₅(FeMn)₃Si₂ phases. This study used scanning electron microscopy to conduct point analyses and elemental mappings of the intermetallics found in the casting and heat treatment samples. Additionally, X-ray diffraction was employed to determine the stoichiometry of the present phases. The results indicated that the cast structure contains β-Al₆FeMn and α-Al₁₅(FeMn)₃Si₂ phases and that the β-Al₆FeMn phase transforms into the α-Al₁₅(FeMn)₃Si₂ phase upon completion of the heat treatment process. By using specific Fe/Mn ratios, the formation of the needle-shaped Al₅FeSi phase in the casting structure of the alloy can be inhibited, leading to the precipitation of phases such as β-Al₆FeMn and α-Al₁₅(FeMn)₃Si₂ instead.

The study of aluminothermic reduction in manganese compounds is a complex challenge in preparing Al-Mn alloys. The primary objective of this study was to ascertain the activation energy values for the aluminothermic reduction of MnO and Mn₃O₄ oxides derived from alkaline batteries. The study melted aluminum found in beverage cans and utilized the technique of powder addition with mechanical agitation. The kinetics of the reaction were studied under the effects of temperature (750, 800, and 850 °C), degree of agitation (200, 250, and 300 rpm), and the initial concentration of magnesium in molten aluminum (1, 2, 3, and 4% by weight). Kinetic measurements for Mn₃O₄ particles suggest a reaction mechanism that occurs in stages, where manganese undergoes oxidation states [Mn⁺³] to [Mn⁺²] until it reaches the oxidation state Mn⁰, which allows it to dissolve in the molten aluminum, forming alloys with up to 1.5 wt.% of Mn. Therefore, the kinetic of the aluminothermic reduction of MnO is described by the geometric contraction model, while the mechanism of Mn₃O₄ reduction occurs in two stages: geometric contraction, followed by an additional stage involving the diffusion of chemical species to the boundary layer. In addition, this stage can be considered a competition between the formation of MnO and the chemical reaction itself.

This paper aimed at studying the effect of magnesium concentration in molten aluminum produced from beverage cans on the process of aluminothermic reduction of Mn₂O₃ particles obtained from the cathodes of discharged alkaline batteries. The experimental results were analyzed by using thermodynamic fundamentals and kinetic modeling, while the characterization of the reaction products obtained allowed the mechanism of the process to be described. It was found that the addition of magnesium improves the wettability of solid particles by molten aluminum, thus increasing the reaction and its subsequent incorporation into the molten aluminum solution of Mn released from the reduction reaction. This work was carried out using several initial magnesium concentrations; 1.0, 2.0, 3.0, and 4.0 wt %, under a constant temperature of 1073 K, a constant treatment time of 240 min, and a constant agitation speed of 200 rpm. The results show that the higher the initial magnesium concentration in the molten alloy, the higher the speed of the chemical reduction reaction of the Mn₂O₃ particles.

The aluminum alloys corresponding to the 6000 series are mainly manufactured by mechanical forming processes. Their properties are enhanced by the homogeneous distribution of intermetallic phases such as β-Al₅FeSi or α-Al_x (Fe, Mn) Si. By thermal homogenization treatment, the intermetallic compound β-Al₅FeSi changes its morphology from a needle type with a monoclinic structure to an acicular form known as α-Al₁₂(Fe, Mn)₃Si with an fcc structure. In the present study, samples of the 6063 alloy were subjected to different temperatures of homogenization (798, 823, and 848 K) and treatment times from 0 to 660 min (in intervals of 30 min) to evaluate their effects on the microstructures and morphologies of the intermetallic phases. For the kinetic study, the microstructures of the β and α intermetallic phases were quantified using the Image-Pro software. The results indicate that as the temperature and homogenization time increase, the percentage of phase α also increments. The results of the kinetic analysis revealed that the β → α transformation is controlled by two stages; the first corresponds to the diffusion of Mn atoms from the matrix to the interface of reaction for the formation of the intermetallic phases, while the second corresponds to the nucleation and growth of the iron- and manganese-rich intermetallic phases.

In this work, the experimental results obtained during the preparation of Al-Ni and Al-Ni-Mg alloys using the aluminothermic reduction of NiO by submerged powder injection, assisted with mechanical agitation are presented and discussed. The analyzed variables were melt temperature, agitation speed, and initial magnesium concentration in the molten alloy. For some of the experiments performed, it was found that the Ni concentration increased from 0 to about 3 wt-% after 90 min of treatment at constant temperature and constant agitation speed. In order to determine the values of the kinetic parameters of interest, such as the activation energy and the rate constants, the values of the results obtained were fitted to the kinetic formulae available. Moreover, the kinetics of the reaction were found to be governed by the diffusion of Al and Mg to the NiO boundary layer, where MgAl₂O₄ or Al₂O₃ were formed as the main reaction products. Finally, from a thermodynamic study of the system, the main reactions that took place are explained.

The design of an aluminium melting furnace has faced two challenges: mathematical modelling and simulative optimization. This paper first uses fluid dynamics to model the aluminium process mathematically. Then, the model is utilized to simulate a round shaped reverberatory furnace for melting aluminium alloys. In order to achieve the highest thermal efficiency of the furnace, modelling and simulation are performed to predict complex flow patterns, geometries, temperature profiles of the mixture-gas air through the main chamber, as well as the melting tower attached to the furnace. The results led to the establishment of optimal position and angle of the burner, which are validated through physical experiments, ensuring recirculation of the combustion gases through the melting chamber and the melting tower. Furthermore, a proper arrangement of refractory materials is derived to avoid heat losses through the outer surface of the furnace. Temperature profiles are also determined for the optimization to arrive at the final design of the furnace. Compared with manual designs previously practiced, the simulation-based optimal design of furnaces offers excellent guidance, an increase in the aluminium processing and magnesium removal for more refined alloys, and an increased processing rate of aluminium chip accession.