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PLASTIC DEFORMATION AND ANISOTROPY OF LONG-PERIOD-STACKING-ORDERED STRUCTURES IN MG-ZN-Y ALLOYS

机译:MG-ZN-Y合金长周期有序结构的塑性变形和各向异性

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Wider application of magnesium alloys as light-weight structural materials requires improvement of strength and toughness. Recently, Mg-Y-Zn and Mg-RE-Zn alloys containing long period stacking ordered (LPSO) structures have received considerable attention, due to their potential to possess excellent mechanical performance at ambient and elevated temperatures. Sharing the same basal plane of α-Mg, LPSO structures are periodically stacked along the c-axis of the hexagonal crystal structure forming so-called 10H, 14H, 18R and 24R structures. LPSO structures are also chemically ordered where Y/RE and Zn atoms replace the positions of Mg atoms in neighboring (0001) planes. The underlying deformation mechanisms of LPSO structures and their co-deformation with α-Mg leading to a concomitant increase of strength and ductility with respect to pure Mg and most commercial Mg alloys are not understood yet. Therefore, we performed micro-pillar compression experiments on 7°(0001), 46°(0001) and 90°(0001) oriented α-Mg and 18R LPSO micro-pillars to investigate the deformation and co-deformation mechanisms of Mg-LPSO alloys. Electron backscatter diffraction-assisted slip trace analysis and post-mortem transmission electron microscopy analysis showed predominant deformation by basal dislocation slip in 46°(0001) and 7°(0001) oriented micro-pillars in both phases, LPSO and a-Mg. In 90°(0001) oriented micro-pillars (1-100)[11-20] prismatic slip was predominantly activated during the early deformation stages. With increasing strain, the formation of kink bands, shear bands and (-211-4)[-4223] deformation twins was observed. The activation energies of basal and prismatic slip are higher for 18R LPSO than for α-Mg. These results shed light on how LPSO structures deform plastically and might be used to purposely design microstructure and texture of Mg-LPSO alloys in the future.
机译:镁合金作为轻质结构材料的广泛应用需要提高强度和韧性。近年来,由于具有在环境和升高的温度下具有优异的机械性能的潜力,包含长期堆叠有序(LPSO)结构的Mg-Y-Zn和Mg-RE-Zn合金受到了广泛的关注。 LPSO结构共享相同的α-Mg基面,沿着六方晶体结构的c轴定期堆叠,形成所谓的10H,14H,18R和24R结构。 LPSO结构在化学上也是有序的,其中Y / RE和Zn原子替换了相邻(0001)平面中Mg原子的位置。相对于纯Mg和大多数市售Mg合金,LPSO结构的潜在变形机理及其与α-Mg的共同变形会导致强度和延展性的同时提高,目前尚不清楚。因此,我们在7°(0001),46°(0001)和90°(0001)取向的α-Mg和18R LPSO微柱上进行了微柱压缩实验,以研究Mg-LPSO的变形和共变形机制合金。电子背散射衍射辅助滑移痕迹分析和验后透射电子显微镜分析显示,在46°(0001)和7°(0001)取向的微柱中,基相位错滑移在LPSO和a-这两个阶段均产生主要变形。镁在变形初期,在90°(0001)取向的微柱(1-100)[11-20]中,棱柱形滑动主要被激活。随着应变的增加,观察到扭结带,剪切带和(-211-4)[-4223]形变孪晶的形成。对于18R LPSO,基和棱柱形滑移的活化能比α-Mg高。这些结果揭示了LPSO结构如何塑性变形,并可能在将来用于有目的地设计Mg-LPSO合金的微观结构和织构。

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