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Effect of Gd content on microstructure and mechanical properties of Mg-xGd-Zr alloys via semicontinuous casting 钆含量对半连续铸造 Mg-xGd-Zr 合金微观结构和机械性能的影响
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-12 DOI: 10.1016/j.jma.2024.10.013
Qianye Wu, Yujuan Wu, Qingchen Deng, Chenyang Ding, Yu Zhang, Nanxi Peng, Licheng Jia, Zhiyu Chang, Liming Peng
Mg-Gd based alloys are an important class of high-performance Mg alloys. In this study, three Mg-Gd alloys with different gadolinium (Gd) contents: Mg-9.54Gd-0.40Zr (wt.%, G10 K), Mg-15.11Gd-0.35Zr (wt.%, G15 K) and Mg-19.67Gd-0.33Zr (wt.%, G20 K) were prepared by semicontinuous casting and subsequent solution and aging heat treatments. The role of Gd content on microstructures and mechanical properties of the Mg-Gd-Zr alloy is studied. All three as-cast alloys exhibit eutectic phases of Mg5Gd, with the amount increasing as the Gd content rises. Mg5Gd disappears after the solution heat treatment (the G10 K alloy solution-treated at 480 °C for 4 h, the G15 K alloy at 500 °C for 12 h and the G20 K alloy at 520 °C for 24 h, respectively). Aging heat treatment at 200 °C for 64 h after solution introduces numerous prismatic β′ precipitates, with a significant increase in their area number density corresponding to increased Gd content. Additionally, the morphology of the β′ precipitates exhibits distinct variations: the G10 K alloy is characterized by an enhanced aspect ratio. Consequently, the peak-aged G10 K alloy demonstrates superior strength-ductility synergy, with a yield strength (YS) of 216 ± 1 MPa, an ultimate tensile strength (UTS) of 363 ± 1 MPa, and an elongation (EL) of 8.7 ± 0.6 %. This study suggests that plasticity diminishes and precipitation strengthening is limited when the gadolinium content exceeds 15 wt.%.
镁钆基合金是一类重要的高性能镁合金。本研究采用了三种不同钆(Gd)含量的镁钆合金:通过半连续铸造以及随后的固溶和时效热处理,制备了三种不同钆(Gd)含量的镁钆合金:Mg-9.54Gd-0.40Zr(重量百分比,G10 K)、Mg-15.11Gd-0.35Zr(重量百分比,G15 K)和 Mg-19.67Gd-0.33Zr(重量百分比,G20 K)。研究了钆含量对 Mg-Gd-Zr 合金微观结构和机械性能的影响。所有三种铸造合金都呈现出 Mg5Gd 共晶相,且随着 Gd 含量的增加而增加。Mg5Gd 在固溶热处理后消失(G10 K 合金分别在 480 ℃ 固溶处理 4 小时,G15 K 合金在 500 ℃ 固溶处理 12 小时,G20 K 合金在 520 ℃ 固溶处理 24 小时)。固溶后在 200 °C 下进行 64 小时的时效热处理会产生大量棱柱形 β′ 沉淀,其面积数密度会随着钆含量的增加而显著增加。此外,β′沉淀的形态也有明显的变化:G10 K 合金的特征是长宽比增大。因此,峰值时效 G10 K 合金显示出卓越的强度-电导率协同作用,屈服强度(YS)为 216 ± 1 MPa,极限拉伸强度(UTS)为 363 ± 1 MPa,伸长率(EL)为 8.7 ± 0.6 %。这项研究表明,当钆含量超过 15 wt.% 时,塑性减弱,沉淀强化受到限制。
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引用次数: 0
Strengthening of Mg-Li alloy dominated by continuously hardened Mg phase during room temperature rolling 室温轧制过程中连续硬化镁相主导的镁锂合金强化
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-12 DOI: 10.1016/j.jma.2024.10.002
Zhonghao Heng, Xianzhe Shi, Lijuan Huang, Biao Chen, Jianghua Shen
The process of room temperature rolling is a straightforward and efficient method for producing high strength Mg-Li alloys, but the underlying strengthening mechanism remains unclear. In this study, we successfully enhanced the tensile properties of a novel dual-phase Mg-Li alloy through room temperature rolling, with a remarkable yield strength of 201 MPa and an elongation-to-failure of 14 %. Microhardness testing was conducted to evaluate the contribution of the Mg- and Li- phases to the improvement in strength. The results demonstrate that the hardness of Mg-phase reaches 60 HV, which is significantly higher than the 49 HV observed in Li-phase, indicating that the Mg-phase after rolling plays a pivotal role in enhancing material strength. The presence of a high density of dislocations stored in the Mg-phase emerges as the dominant factor contributing to improved strength in Mg-Li alloys. In-situ compression testing reveals that 〈c + a〉 slip activation and twinning-induced slip serve as internal mechanisms for continuous deformation and hardening within the Mg-phase. Despite numerous precipitated Mg-phase particles within the Li-phase matrix, the hardness analysis reveals minimal strain-induced phase transformation effects on the overall strength of the Al-free and Zn-free Mg-Li alloy. These findings provide valuable insights for designing and fabricating high-strength dual-phase Mg-Li alloys.
室温轧制工艺是生产高强度镁锂合金的一种直接而高效的方法,但其潜在的强化机制仍不清楚。在本研究中,我们通过室温轧制成功提高了新型双相镁锂合金的拉伸性能,屈服强度达到 201 兆帕,伸长率达到 14%。为了评估镁相和锂相对强度提高的贡献,还进行了显微硬度测试。结果表明,镁相的硬度达到 60 HV,明显高于锂相的 49 HV,这表明轧制后的镁相在提高材料强度方面发挥了关键作用。储存在镁相中的高密度位错是提高镁锂合金强度的主要因素。原位压缩测试表明,〈c + a〉滑移激活和孪生诱导滑移是镁相内持续变形和硬化的内部机制。尽管锂相基体中存在大量析出的镁相颗粒,但硬度分析显示,应变诱导相变对无铝无锌镁锂合金整体强度的影响微乎其微。这些发现为设计和制造高强度双相镁锂合金提供了宝贵的启示。
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引用次数: 0
Revealing Hetero-Deformation Induced (HDI) Hardening and Dislocation Activity in a Dual-Heterostructure Magnesium Matrix Composite 揭示双异质结构镁基复合材料中的异质变形诱导(HDI)硬化和位错活性
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-12 DOI: 10.1016/j.jma.2024.10.012
Lingling Fan, Ran Ni, Lingbao Ren, Peng Xiao, Ying Zeng, Dongdi Yin, Hajo Dieringa, Yuanding Huang, Gaofeng Quan, Wei Feng
Integrating a heterogeneous structure can significantly enhance the strength-ductility synergy of composites. However, the relationship between hetero-deformation induced (HDI) strain hardening and dislocation activity caused by heterogeneous structures in the magnesium matrix composite remains unclear. In this study, a dual-heterogeneous TiC/AZ61 composite exhibits significantly improved plastic elongation (PEL) by nearly one time compared to uniform FG composite, meanwhile maintaining a high strength (UTS: 417 MPa). This is because more severe deformation inhomogeneity in heterogeneous structure leads to more geometrically necessary dislocations (GNDs) accumulation and stronger HDI stress, resulting in higher HDI hardening compared to FG and CG composites. During the early stage of plastic deformation, the pile-up types of GND in the FG zone and CG zone are significantly different. GNDs tend to form substructures in the FG zone instead of the CG zone. They only accumulate at grain boundaries of the CG region, thereby leading to obviously increased back stress in the CG region. In the late deformation stage, the elevated HDI stress activates the new 〈c + a〉 dislocations in the CG region, resulting in dislocation entanglements and even the formation of substructures, further driving the high hardening in the heterogeneous composite. However, For CG composite, 〈c + a〉 dislocations are not activated even under large plastic strains, and only 〈a〉 dislocations pile up at grain boundaries and twin boundaries. Our work provides an in-depth understanding of dislocation variation and HDI hardening in heterogeneous magnesium-based composites.
整合异质结构可显著提高复合材料的强度-电导率协同效应。然而,镁基复合材料中异质结构引起的异质变形诱导(HDI)应变硬化与位错活动之间的关系仍不清楚。在本研究中,与均匀 FG 复合材料相比,双异质 TiC/AZ61 复合材料的塑性延伸率(PEL)显著提高了近一倍,同时保持了较高的强度(UTS:417 兆帕)。这是因为与 FG 和 CG 复合材料相比,异质结构中更严重的变形不均匀性导致更多的几何必要位错(GNDs)积累和更强的 HDI 应力,从而产生更高的 HDI 硬化。在塑性变形的早期阶段,FG 区和 CG 区的 GND 堆积类型明显不同。GND 往往在 FG 区而不是 CG 区形成亚结构。它们只在 CG 区的晶界处堆积,从而导致 CG 区的背应力明显增加。在变形后期,HDI应力的升高激活了CG区新的〈c + a〉位错,导致位错缠结,甚至形成亚结构,进一步推动了异质复合材料的高硬化。然而,对于CG复合材料,〈c + a〉位错即使在大塑性应变下也不会被激活,只有〈a〉位错堆积在晶界和孪晶边界。我们的研究深入了解了异质镁基复合材料中的位错变化和高密度互连硬化。
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引用次数: 0
Grain refinement, twin formation and mechanical properties of magnesium welds with addition of CNTs and TiC particles 添加 CNT 和 TiC 粒子后镁焊缝的晶粒细化、孪晶形成和力学性能
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-12 DOI: 10.1016/j.jma.2024.10.009
Yongkang Gao, Lianyong Xu, Kangda Hao, Yongdian Han, Lei Zhao, Wenjing Ren
In this work, microstructure and mechanical properties of Mg weld with addition of carbon nanotubes (CNTs) and TiC particles were investigated. The results showed that the weld microstructure was mainly presented as equiaxed grains with almost high angle grain boundaries. The introduction of reinforcements promoted the formation of precipitates and refined the grains effectively, the average grain size was refined by 51 % and 23 % with addition of CNTs and TiC particles, respectively. The dislocation density and the fraction of CSL boundaries were increased with addition of CNTs, while those were decreased with addition of TiC particles. Besides, the infrequent {101¯3} contraction twins formed within the weld due to the stress concentration caused by dislocation accumulation, which contributed to the Σ29 CSL boundary. The ultimate tensile strength and elongation rate were increased by 13.5 % and 40 % with addition of CNTs, while the ultimate tensile strength and micro-hardness were increased by 14.8 % and 20.9 % with addition of TiC particles.
本文研究了添加碳纳米管(CNT)和 TiC 粒子的镁焊缝的微观结构和机械性能。结果表明,焊缝的微观结构主要表现为等轴晶粒,晶界几乎呈高角度。添加 CNTs 和 TiC 粒子后,平均晶粒尺寸分别细化了 51% 和 23%。添加 CNTs 后,位错密度和 CSL 边界比例增加,而添加 TiC 粒子后,位错密度和 CSL 边界比例降低。此外,由于位错堆积导致的应力集中,焊缝内部形成了不常见的{101¯1¯3}收缩孪晶,从而形成了Σ29 CSL边界。添加 CNTs 后,极限拉伸强度和伸长率分别提高了 13.5 % 和 40 %;添加 TiC 颗粒后,极限拉伸强度和显微硬度分别提高了 14.8 % 和 20.9 %。
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引用次数: 0
On the origin of non-basal texture in extruded Mg-RE alloys and its implication for texture engineering 挤压 Mg-RE 合金非基质纹理的起源及其对纹理工程的影响
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-12 DOI: 10.1016/j.jma.2024.10.004
X.Z. Jin, G.J. Yang, Xinyu Xu, D.B. Shan, B. Guo, B.B. He, C. Fan, W.C. Xu
The work aims to investigate the formation and transformation mechanism of non-basal texture in the extruded Mg alloys. With this purpose a pure Mg as reference and eight Mg-Gd binary alloys with the Gd concentration ranging from 0.5 wt.% to 18 wt.% were prepared for extrusion. This study shows that the basal fiber texture in pure Mg transited into RE (rare earth) texture in diluted Mg-Gd alloys and into the abnormal C-texture in high-concentration Mg-Gd alloys. In pure Mg, discontinuous dynamic recrystallization plays a predominant role during the extrusion process, resulting in the formation of a typical basal fiber texture. Alloying with high concentration of Gd impedes the dynamic recrystallization process, facilitating the heterogeneous nucleation of shear bands as well as the dynamic recrystallization within shear bands. Dynamic recrystallized grains within shear bands nucleate with a similar orientation to the host deformed parent grains and gradually tilt their c-axis to the extrusion direction during growth by absorbing dislocations, leading to the formation of either the RE-texture orientation or the C-texture orientation, depending on the stored energy within shear bands. The analysis aided by IGMA and TEM characterization reveals that the shear bands originate from the extensive but heterogeneous activation of pyramidal I slip. Tensile tests illustrate a close correlation between the fracture elongation and texture types. A comprehensive understanding of the formation and transformation mechanism of different texture components in Mg alloys holds significant importance for the design of high-performance Mg alloys by texture engineering.
这项工作旨在研究挤压镁合金中非基态纹理的形成和转变机制。为此,以纯镁为参照物,制备了八种镁钆二元合金(钆浓度范围为 0.5 wt.%-18wt.%)进行挤压。研究表明,在稀释的镁钆合金中,纯镁的基底纤维纹理转变为稀土(RE)纹理,而在高浓度镁钆合金中则转变为异常的 C 型纹理。在纯镁中,不连续动态再结晶在挤压过程中起主导作用,从而形成典型的基底纤维纹理。高浓度钆合金阻碍了动态再结晶过程,促进了剪切带的异质成核以及剪切带内的动态再结晶。剪切带内的动态再结晶晶粒的成核取向与寄主变形母晶粒相似,并在生长过程中通过吸收位错使其 c 轴逐渐向挤压方向倾斜,从而形成 RE 纹理取向或 C 纹理取向,具体取决于剪切带内的存储能量。通过 IGMA 和 TEM 表征分析发现,剪切带源于金字塔 I 滑移的广泛但异质的激活。拉伸试验表明,断裂伸长率与纹理类型密切相关。全面了解镁合金中不同纹理成分的形成和转变机制,对于通过纹理工程设计高性能镁合金具有重要意义。
{"title":"On the origin of non-basal texture in extruded Mg-RE alloys and its implication for texture engineering","authors":"X.Z. Jin, G.J. Yang, Xinyu Xu, D.B. Shan, B. Guo, B.B. He, C. Fan, W.C. Xu","doi":"10.1016/j.jma.2024.10.004","DOIUrl":"https://doi.org/10.1016/j.jma.2024.10.004","url":null,"abstract":"The work aims to investigate the formation and transformation mechanism of non-basal texture in the extruded Mg alloys. With this purpose a pure Mg as reference and eight Mg-Gd binary alloys with the Gd concentration ranging from 0.5 wt.% to 18 wt.% were prepared for extrusion. This study shows that the basal fiber texture in pure Mg transited into RE (rare earth) texture in diluted Mg-Gd alloys and into the abnormal C-texture in high-concentration Mg-Gd alloys. In pure Mg, discontinuous dynamic recrystallization plays a predominant role during the extrusion process, resulting in the formation of a typical basal fiber texture. Alloying with high concentration of Gd impedes the dynamic recrystallization process, facilitating the heterogeneous nucleation of shear bands as well as the dynamic recrystallization within shear bands. Dynamic recrystallized grains within shear bands nucleate with a similar orientation to the host deformed parent grains and gradually tilt their c-axis to the extrusion direction during growth by absorbing dislocations, leading to the formation of either the RE-texture orientation or the C-texture orientation, depending on the stored energy within shear bands. The analysis aided by IGMA and TEM characterization reveals that the shear bands originate from the extensive but heterogeneous activation of pyramidal I slip. Tensile tests illustrate a close correlation between the fracture elongation and texture types. A comprehensive understanding of the formation and transformation mechanism of different texture components in Mg alloys holds significant importance for the design of high-performance Mg alloys by texture engineering.","PeriodicalId":16214,"journal":{"name":"Journal of Magnesium and Alloys","volume":"95 1","pages":""},"PeriodicalIF":17.6,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142601112","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Cation-induced topical disordered niobium nickel oxide for robust hydrogen storage in magnesium hydride 阳离子诱导的局部无序氧化铌镍在氢化镁中实现稳健储氢
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-09 DOI: 10.1016/j.jma.2024.10.011
Shuai Li, Liuting Zhang, Fuying Wu, Qian Li
Catalytic doping is one of the economic and efficient strategies to optimize the operating temperature and kinetic behavior of magnesium hydride (MgH2). Herein, efficient regulation of electronic and structural rearrangements in niobium-rich nickel oxides was achieved through precise compositional design and niobium cation functionalized doping, thereby greatly enhancing its intrinsic catalytic activity in hydrogen storage systems. As the niobium concentration increased, the Ni-Nb catalysts transformed into a mixed state of multi-phase nanoparticles (composed of nickel and niobium-rich nickel oxides) with smaller particle size and uniform distribution, thus exposing more nucleation sites and diffusion channels at the MgH2/Mg interface. In addition, the additional generation of active Ni-Nb-O mixed phase induced numerous highly topical disordered and distorted crystalline, promoting the transfer and reorganization of H atoms. As a result, a stable and continuous multi-phase/component synergistic catalytic microenvironment could be constructed, exerting remarkable enhancement on MgH2's hydrogen storage performance. After comparative tests, Ni0.7Nb0.3-doped MgH2 presented the optimal low-temperature kinetics with a dehydrogenation activation energy of 78.8 kJ·mol−1. The onset dehydrogenation temperature of MgH2+10 wt% Ni0.7Nb0.3 was reduced to 198 °C and 6.18 wt% H2 could be released at 250 °C within 10 min. In addition, the dehydrogenated MgH2single bondNiNb composites absorbed 4.87 wt% H2 in 10 min at 125 °C and a capacity retention rate was maintained at 6.18 wt% even after 50 reaction cycles. In a word, our work supplies fresh insights for designing novel defective-state multiphase catalysts for hydrogen storage and other energy related field.
催化掺杂是优化氢化镁(MgH2)操作温度和动力学行为的经济而有效的策略之一。在这里,通过精确的成分设计和铌阳离子功能化掺杂,实现了对富铌镍氧化物中电子和结构重排的有效调节,从而大大提高了其在储氢系统中的内在催化活性。随着铌浓度的增加,镍-铌催化剂转变为粒径更小、分布更均匀的多相纳米颗粒(由镍和富铌镍氧化物组成)的混合状态,从而在 MgH2/Mg 界面暴露出更多的成核点和扩散通道。此外,活性镍-铌-氧化物混合相的额外生成诱导了大量高度拓扑无序和扭曲的晶体,促进了 H 原子的转移和重组。因此,可以构建一个稳定、连续的多相/组分协同催化微环境,显著提高 MgH2 的储氢性能。经过对比试验,掺杂 Ni0.7Nb0.3 的 MgH2 具有最佳的低温动力学性能,其脱氢活化能为 78.8 kJ-mol-1。MgH2+10 wt% Ni0.7Nb0.3的起始脱氢温度降低到198 °C,在250 °C的温度下,10分钟内可释放出6.18 wt%的H2。此外,脱氢的 MgH2NiNb 复合材料在 125 ℃ 下 10 分钟内吸收了 4.87 wt% 的 H2,即使经过 50 个反应循环,容量保持率仍为 6.18 wt%。总之,我们的工作为设计新型缺陷态多相催化剂用于储氢和其他能源相关领域提供了新的见解。
{"title":"Cation-induced topical disordered niobium nickel oxide for robust hydrogen storage in magnesium hydride","authors":"Shuai Li, Liuting Zhang, Fuying Wu, Qian Li","doi":"10.1016/j.jma.2024.10.011","DOIUrl":"https://doi.org/10.1016/j.jma.2024.10.011","url":null,"abstract":"Catalytic doping is one of the economic and efficient strategies to optimize the operating temperature and kinetic behavior of magnesium hydride (MgH<sub>2</sub>). Herein, efficient regulation of electronic and structural rearrangements in niobium-rich nickel oxides was achieved through precise compositional design and niobium cation functionalized doping, thereby greatly enhancing its intrinsic catalytic activity in hydrogen storage systems. As the niobium concentration increased, the Ni-Nb catalysts transformed into a mixed state of multi-phase nanoparticles (composed of nickel and niobium-rich nickel oxides) with smaller particle size and uniform distribution, thus exposing more nucleation sites and diffusion channels at the MgH<sub>2</sub>/Mg interface. In addition, the additional generation of active Ni-Nb-O mixed phase induced numerous highly topical disordered and distorted crystalline, promoting the transfer and reorganization of H atoms. As a result, a stable and continuous multi-phase/component synergistic catalytic microenvironment could be constructed, exerting remarkable enhancement on MgH<sub>2</sub>'s hydrogen storage performance. After comparative tests, Ni<sub>0.7</sub>Nb<sub>0.3</sub>-doped MgH<sub>2</sub> presented the optimal low-temperature kinetics with a dehydrogenation activation energy of 78.8 kJ·mol<sup>−1</sup>. The onset dehydrogenation temperature of MgH<sub>2</sub>+10 wt% Ni<sub>0.7</sub>Nb<sub>0.3</sub> was reduced to 198 °C and 6.18 wt% H<sub>2</sub> could be released at 250 °C within 10 min. In addition, the dehydrogenated MgH<sub>2</sub><img alt=\"single bond\" src=\"https://sdfestaticassets-us-east-1.sciencedirectassets.com/shared-assets/55/entities/sbnd.gif\" style=\"vertical-align:middle\"/>NiNb composites absorbed 4.87 wt% H<sub>2</sub> in 10 min at 125 °C and a capacity retention rate was maintained at 6.18 wt% even after 50 reaction cycles. In a word, our work supplies fresh insights for designing novel defective-state multiphase catalysts for hydrogen storage and other energy related field.","PeriodicalId":16214,"journal":{"name":"Journal of Magnesium and Alloys","volume":"105 1","pages":""},"PeriodicalIF":17.6,"publicationDate":"2024-11-09","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142597024","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mechanism of work hardening and softening behavior of AZ31 magnesium alloy sheets with hard plate accumulative roll bonding 硬板累积轧制结合 AZ31 镁合金板材的加工硬化和软化行为机理
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-09 DOI: 10.1016/j.jma.2024.10.003
Lu Sun, Feng Li, Jia Yang Zhang, Wen Tao Niu, Mu Zi Cao
In this paper, the work hardening and softening behavior of AZ31 magnesium alloy sheets by hard plate accumulative roll bonding (HP-ARB) process in a specific temperature range was studied for the first time, and the cyclic stress relaxation test, EBSD, TEM and other characterization methods were used. When the rolling temperature is 350 °C, the grain size of magnesium sheets is refined to 4.32 (±0.36) µm on average, and it shows an excellent combination of strength and plasticity. The tensile strength reaches 307 (±8.52) MPa and the elongation is 12.73 (±0.84) %. At this time, the curve of work hardening rate decreases smoothly and the degree of hardening is the lowest, and the amplitude of stress drop Δσp in work softening test is the smallest with the increase of cycle times, which shows that the well coordination between work hardening and softening behavior has been achieved. Research has found that the combined effect of grain boundary strengthening and fine grain strengthening enhances the yield and tensile strength of magnesium sheets after three passes HP-ARB process at 350 °C. This is attributed to the high degree of dislocation slip opening in the pyramidal surface 〈a〉 and 〈c + a〉, which not only coordinates the c-axis strain of the entire grain, but also promotes the slip transfer of dislocations in the fine-grained region, significantly improving the elongation of the sheets. This study provides a new idea for the forming and manufacturing of high performance magnesium alloy sheets.
本文首次采用硬板累积轧制结合(HP-ARB)工艺研究了 AZ31 镁合金板材在特定温度范围内的加工硬化和软化行为,并采用了循环应力松弛试验、EBSD、TEM 等表征方法。当轧制温度为 350 ℃ 时,镁板的晶粒尺寸平均细化至 4.32 (±0.36) µm,并显示出极佳的强度和塑性组合。拉伸强度达到 307 (±8.52) 兆帕,伸长率为 12.73 (±0.84) %。此时,随着循环次数的增加,加工硬化率曲线平稳下降,硬化程度最低,加工软化试验中的应力下降幅度Δσp最小,这表明加工硬化和软化行为之间实现了良好的协调。研究发现,晶界强化和细晶粒强化的共同作用提高了镁板在 350 °C 下经过三道 HP-ARB 工艺后的屈服强度和抗拉强度。这归功于金字塔形表面〈a〉和〈c + a〉的位错滑移开口度高,不仅协调了整个晶粒的c轴应变,还促进了细晶粒区位错的滑移转移,显著提高了板材的伸长率。这项研究为高性能镁合金板材的成形和制造提供了新思路。
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引用次数: 0
Quasi-in situ electron backscatter diffraction analysis of twinning–detwinning behavior in AZ31 magnesium- alloy rolled plates subjected to compression loading in different directions 不同方向压缩加载下 AZ31 镁合金轧制板中孪晶-脱晶行为的准原位电子反向散射衍射分析
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-07 DOI: 10.1016/j.jma.2024.10.007
Le Zhou, Guiyuan Ren, Tianqi Huang, Zhi Wang, Feng Wang, Ziqi Wei, Pingli Mao, Zheng Liu
In this study, the twinning–detwinning behavior and slip behavior of rolled AZ31 magnesium-alloy plates during a three-step intermittent dynamic compression process along the rolling direction (RD) and normal direction (ND), are investigated via quasi-in situ electron backscatter diffraction, and the causes of the twinning and detwinning behavior are explained according to Schmid law, local strain coordination, and slip trajectories. It is found that the twins are first nucleated and grow at a compressive strain of 3% along the RD. In addition to the Schmid factor (SF), the strain coordination factor (m') also influences the selection of the twin variants during the twinning process, resulting in the nucleation of twins with a low SF. During the second and third steps of the application of continuous compressive strains with magnitudes and directions of 3%RD+3%ND and 3%RD+3%ND+2.5%ND, detwinning occurs to different extents. The observation of the detwinning behavior reveals that the order in which multiple twins within the same grain undergo complete detwinning is related to Schmid law and the strain concentration, with a low SF and a high strain concentration promoting complete detwinning. The interaction between slip dislocations and twin boundaries in the deformed grains as well as the pinning of dislocations at the tips of the {101¯2} tensile twins with a special structure result in incomplete detwinning. Understanding the microstructural evolution and twinning behavior of magnesium alloys under different deformation geometries is important for the development of high-strength and high-toughness magnesium alloys.
本研究通过准原位电子反向散射衍射,研究了轧制的 AZ31 镁合金板材在三步间歇动态压缩过程中沿轧制方向(RD)和法线方向(ND)的孪晶-脱晶行为和滑移行为,并根据施密德定律、局部应变协调和滑移轨迹解释了孪晶和脱晶行为的原因。研究发现,孪晶首先成核,并在沿 RD 3% 的压缩应变下生长。在孪生过程中,除了施密德因子(SF)外,应变协调因子(m')也会影响孪生变体的选择,导致低施密德因子的孪生成核。在施加幅度和方向分别为 3%RD+3%ND 和 3%RD+3%ND+2.5%ND 的连续压缩应变的第二和第三步中,脱孪现象在不同程度上发生。对脱赢行为的观察表明,同一晶粒内多个孪晶发生完全脱赢的顺序与施密德定律和应变浓度有关,低SF和高应变浓度会促进完全脱赢。变形晶粒中滑移位错和孪晶边界之间的相互作用以及具有特殊结构的{101¯1¯2}拉伸孪晶顶端的位错钉扎导致了不完全脱晶。了解镁合金在不同变形几何条件下的微结构演变和孪晶行为对开发高强度和高韧性镁合金具有重要意义。
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引用次数: 0
Precipitation-strengthened micromechanical behaviors of magnesium alloy under cyclic loading 循环加载下镁合金的沉淀强化微机械行为
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-04 DOI: 10.1016/j.jma.2024.09.008
Chuhao Liu, Di Xie, Yanfei Gao, Xiaodan Zhang, Shengyi Zhong, Huamiao Wang, Ke An, Peter K. Liaw, Yinghong Peng
The microscopic-deformation mechanisms of an extruded magnesium alloy with and without precipitates [Guinier-Preston (GP) zones] subjected to cyclic deformation were investigated by in-situ neutron-diffraction (ND) measurements and crystal-plasticity modeling. The relationship between the macroscopic-cyclic-deformation behavior and the microscopic responses (particularly twinning and detwinning) at the grain level was established. The general deformation-mechanism evolution in the solution-state (ST) sample was similar to that in the peak-aged-state (PA) sample over fatigue cycles. Both samples plastically deformed by extension twinning during compression, and by a sequential process of detwinning and dislocation motion under reverse tension. The main difference is that in the PA sample, the presence of precipitating particles constrains the twinning/detwinning behaviors, which leads to an increase in the participation of dislocation slip in the plastic deformation and then induces a strengthening effect during cyclic loading. Based on the combination of the previous in-situ ND results and crystal-plasticity model, our work provides a comprehensive analysis of the interaction between the precipitation strengthening and twinning/detwinning mechanism under the whole multi-cycle cyclic loading and their effect on the macro- and micro-mechanical behavior of the precipitate-strengthened magnesium alloys.
通过原位中子衍射(ND)测量和晶体塑性建模,研究了有沉淀物和无沉淀物[Guinier-Preston(GP)区]的挤压镁合金在循环变形下的微观变形机制。建立了宏观循环变形行为与晶粒级微观反应(尤其是孪晶和脱晶)之间的关系。在疲劳循环过程中,溶液态(ST)样品的一般变形机制演变与峰值老化态(PA)样品相似。两种样品在压缩过程中都通过拉伸孪晶产生塑性变形,而在反向拉伸过程中则通过连续的脱翅和位错运动产生塑性变形。主要区别在于,在 PA 样品中,沉淀颗粒的存在限制了孪生/脱孪行为,导致位错滑移在塑性变形中的参与度增加,进而在循环加载过程中产生强化效应。结合之前的原位 ND 结果和晶体塑性模型,我们的工作全面分析了在整个多循环周期加载下沉淀强化和孪晶/脱晶机制之间的相互作用,以及它们对沉淀强化镁合金宏观和微观力学行为的影响。
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引用次数: 0
Breaking Mg matrix composite property trade-offs via in-situ interface reaction and heterogeneous structure design 通过原位界面反应和异质结构设计打破镁基复合材料的性能权衡
IF 17.6 1区 材料科学 Q1 METALLURGY & METALLURGICAL ENGINEERING Pub Date : 2024-11-02 DOI: 10.1016/j.jma.2024.10.008
Z.Y. Xu, Y.Q. You, Q. Lu, C.J. Li, M. Song, J. Tan, L. Liu, X.F. Chen, J.H. Yi
Many properties of Mg matrix composites are mutually incompatible, and even completely repel each other. Here, we constructed a magnetic layered component in Mg matrix composite reinforced with reduced graphene oxide (RGO) through an in-situ interface reaction strategy, achieving simultaneous improvement in the strength, ductility, and electromagnetic shielding performance of the composite. The magnetic component is generated by the in-situ reaction of Fe2O3 nanoparticles encapsulated on RGO with the Mg matrix. The superior strength-ductility synergy originates from layered heterostructure, which actives non-basal dislocations and enables a stable microcrack-multiplication. The heterogeneous layered structure strengthens the multi-level reflection of electromagnetic wave (EMW) inside the composite. The in-situ interfacial reaction introduces abundant of heterogeneous interfaces into the composites, which improves the interfacial polarization loss ability of the composites. The magnetic RGO layer can provide shape anisotropy that breaks the Snoek limit, thus improving the magnetic loss ability of composite in high-frequency electromagnetic fields. The synergistic action of multiple EMW loss mechanisms improves the electromagnetic shielding performance of composite. The current study emphasizes the influence of interface structure on the mechanical and functional properties of composites, and presents a promising approach for the development of structure/functional integrated composites with enhanced properties.
镁基复合材料的许多性能互不兼容,甚至完全相斥。在这里,我们通过原位界面反应策略,在用还原氧化石墨烯(RGO)增强的镁基复合材料中构建了磁性层状成分,实现了复合材料强度、延展性和电磁屏蔽性能的同步提高。磁性成分是由封装在 RGO 上的 Fe2O3 纳米颗粒与镁基体原位反应产生的。卓越的强度-电导率协同作用源于分层异质结构,它激活了非基底位错,并实现了稳定的微裂纹增殖。异质层状结构增强了复合材料内部电磁波(EMW)的多级反射。原位界面反应为复合材料引入了丰富的异质界面,提高了复合材料的界面极化损耗能力。磁性 RGO 层可提供打破斯诺克极限的形状各向异性,从而提高复合材料在高频电磁场中的磁损耗能力。多种电磁波损耗机制的协同作用提高了复合材料的电磁屏蔽性能。本研究强调了界面结构对复合材料机械和功能特性的影响,为开发性能更强的结构/功能一体化复合材料提供了一种可行的方法。
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引用次数: 0
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Journal of Magnesium and Alloys
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