The evolution of microstructure, texture, and mechanical properties of an Mg–1.43Nd (wt%) alloy is investigated after processing by high‐pressure torsion at room temperature through five turns and isochronal annealing for 1 h at 150, 250, 350, and 450 °C using electron backscatter diffraction and Vickers microhardness. The alloy exhibits a good thermal stability up to annealing at 250 °C, with mean grain size of ≈0.65 μm. The microhardness shows an initial hardening after annealing at 150 °C and then a subsequent softening. The deformation texture, a basal texture shifted 60° away from the shear direction (SD), is retained during annealing up to 250 °C. In contrast, a basal texture with symmetrical splitting toward SD is developed after annealing at 350 °C. The precipitation sequence and their pinning effects are responsible for the age‐hardening, stabilization of grain size, and the texture modification. The kinetics of grain growth in the Mg–1.43Nd alloy follows two stages depending on the temperature annealing range, with an activation energy of ≈26 kJ mol−1 in the low temperature range of 150–250 °C and ≈147 kJ mol−1 in the high temperature range of 250–450 °C.
The corrosion behaviour of Mg-0.3Ce, Mg-0.41Dy, Mg-0.63Gd, Mg-1.44Nd and Mg-1.43La (wt.%) alloys in 3.5 wt.% NaCl solution was investigated using electrochemical tests. The ascast microstructures of the Mg-RE alloys were characterized by the presence of second phases (MgxCe, Mg41Dy5, Mg12Gd, Mg12Nd, Mg41Nd5, Mg24Nd and Mg12La) with different volume fraction and distribution. Results show that the corrosion mechanism was altered from uniform to localized corrosion mechanism depending on the specific RE alloying elements.The corrosion resistance of the Mg-RE alloys is increasing in the following order: Mg-1.43La, Mg-1.44Nd, Mg-0.3Ce, Mg-0.63Gd and Mg-0.41Dy. Accordingly, the corrosion morphology in the best resistant Mg-0.41Dy alloy and the worst Mg-1.43La alloy were observed and compared after 2h and 24 h of immersion using SEM-EDS, XPS and XRD analysis. The formation of the Dy2O3 oxide prevents the Mg-0.41Dy alloy from pitting corrosion and lead to an excellent corrosion surface even after 24 h of immersion. Meanwhile, the presence of a high fraction of the Mg12La phase along the grains boundaries in the Mg-1.43La alloy causes severe pitting corrosion by acting as anodic phase.
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