研究課題/領域番号 |
22KF0310
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補助金の研究課題番号 |
22F22720 (2022)
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研究種目 |
特別研究員奨励費
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配分区分 | 基金 (2023) 補助金 (2022) |
応募区分 | 外国 |
審査区分 |
小区分18010:材料力学および機械材料関連
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研究機関 | 九州大学 |
研究代表者 |
陳 強 九州大学, 工学研究院, 教授 (30264451)
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研究分担者 |
CHEN YAO 九州大学, 工学研究院, 外国人特別研究員
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研究期間 (年度) |
2023-03-08 – 2025-03-31
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研究課題ステータス |
交付 (2023年度)
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配分額 *注記 |
2,200千円 (直接経費: 2,200千円)
2024年度: 600千円 (直接経費: 600千円)
2023年度: 1,100千円 (直接経費: 1,100千円)
2022年度: 500千円 (直接経費: 500千円)
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キーワード | Mg-RE alloy / Very high cycle fatigue / Crack initiation / Oxidation / Oxygen embrittlement |
研究開始時の研究の概要 |
The proposed research is to undertake quasi-in situ fatigue observation to characterize fatigue transitions from a crack-free stage to a cracked stage, and further short crack growth stage. This study aims at revealing dislocation structures associated with nucleation of microcracks and connecting atomic scale deformation with macroscopic fatigue performance.
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研究実績の概要 |
We investigated the very high cycle fatigue behavior of a Mg alloy with long-period stacking ordered (LPSO) phase. Fatigue fracture and damage observation revealed that microcracks nucleate from the thick alpha-Mg layers, away from the dense LPSO lamellae. Notably, microcrack nucleation was observed inside the localized oxides. This investigation highlights the critical role of highly localized oxide thickening, orders of magnitude thicker than native oxide, in the process of microcrack nucleation. The proposed model reaffirms the importance of the extrusion/intrusion process, but more importantly highlights a mechanism in which fatigue-induced oxidation results in the embrittlement of the extrusion/intrusion structure, which in turn affects the nucleation of microcracks.
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現在までの達成度 (区分) |
現在までの達成度 (区分)
2: おおむね順調に進展している
理由
As planned, macroscopic fatigue strength and damage evolution investigation have been conducted on the Mg/LPSO alloy after solution hot treatment. The results obtained have been submitted to the journal of Scripta Materialia. Further research will be conducted to investigate the plastic localization according to the hierarchical anisotropic nanostructures during fatigue crack nucleation, as well as the microstructural mechanisms involved in the early propagation of microcracks. On the whole, we have achieved the research goals set up for FY2022, and the progress of the project was partially advanced.
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今後の研究の推進方策 |
T-EBSD and AC-STEM will be utilized to investigate the impact of the hierarchical anisotropic nanostructures and the aging heat treatment on the mechanism of microcrack nucleation, especially fatigue-induced oxidation process. By identifying critical microstructure configurations, we will establish a correlation between the configurations and the mechanism of microcrack nucleation. This, in turn, will provide novel insights into the design of microstructures that can enhance the fatigue damage resistance of Mg-RE alloys.
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