Thermodynamic origin of solute-enriched stacking-fault in dilute Mg-Zn-Y alloys
書誌事項
- 公開日
- 2020-03
- 資源種別
- journal article
- 権利情報
-
- https://www.elsevier.com/tdm/userlicense/1.0/
- https://www.elsevier.com/legal/tdmrep-license
- http://creativecommons.org/licenses/by/4.0/
- DOI
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- 10.1016/j.matdes.2019.108452
- 10.2139/ssrn.3411750
- 10.48550/arxiv.1906.05176
- 公開者
- Elsevier BV
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説明
We investigate thermodynamic behaviors of dilute Mg-Zn-Y ternary alloys to form a unique solute-enriched stacking-fault (SESF), which is an intrinsic-II type stacking-fault (I2-SF) enriched by the Zn and Y atoms and represents the structural-unit of the long-period stacking/order (LPSO) phase. SESF in the hexagonal-close-packed (hcp) Mg matrix forms a local face-centered-cubic (fcc) environment, and hence our thermodynamic analysis is based on the Gibbs energy comparison between hcp and fcc phases over the Mg-Zn-Y ternary composition ranges, using the calculation of phase diagrams (CALPHAD) method aided by the first principles calculations. Segregation behaviors of solute Zn/Y atoms into the SESF are firstly estimated according to the Hillert's parallel tangent law, followed by the possible disorder-order phase transformation within the SESF using the multiple-sublattice model. We find that the Zn/Y co-segregations at the SESF provide a remarkable condition that the fcc layers become more stable than the hcp-Mg matrix. Besides, within the SESF, the following spinodal-like decomposition into the Mg-rich solid-solution and the Zn/Y-rich L12-type order phase causes a significant reduction of the total Gibbs energy of the system. These thermodynamic behaviors explain fairly well a phenomenological origin of the Zn-Y clustering with the L12-type short-range order, which is known to occur for the LPSO phases and also confirmed for the present SESF by electron microscopy experiments. Therefore, strong Zn-Y interactions even in dilute conditions play a key role to stabilize firmly the SESF in the Mg-Zn-Y alloys.
53 pages, 10 figures, 4 tables; submitted to Acta Materialia
収録刊行物
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- Materials & Design
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Materials & Design 188 108452-, 2020-03
Elsevier BV
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詳細情報 詳細情報について
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- CRID
- 1361412891995360896
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- ISSN
- 15565068
- 02641275
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- 資料種別
- journal article
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- データソース種別
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