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Acta Metall Sin  2025, Vol. 61 Issue (12): 1803-1816    DOI: 10.11900/0412.1961.2024.00230
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Effect of Long-Period Stacking Ordered Phase Content on the Corrosion Resistance of As-Extruded Mg-Y-Zn-Mn Alloy
JIANG Shujia1, YANG Hongran1, LI Chuanqiang1(), WANG Naiguang1, WANG Desheng2,3()
1 School of Materials and Energy, Guangdong University of Technology, Guangzhou 510006, China
2 National Key Laboratory of Marine Corrosion and Protection, Luoyang Ship Material Research Institute, Luoyang 471023, China
3 School of Materials Science and Engineering, Shanghai Jiao Tong University, Shanghai 200240, China
Cite this article: 

JIANG Shujia, YANG Hongran, LI Chuanqiang, WANG Naiguang, WANG Desheng. Effect of Long-Period Stacking Ordered Phase Content on the Corrosion Resistance of As-Extruded Mg-Y-Zn-Mn Alloy. Acta Metall Sin, 2025, 61(12): 1803-1816.

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Abstract  

Mg alloys with high-strength and long-period stacking ordered (LPSO) phases are promising materials for lightweight structural applications because of their exceptional properties. However, corrosion remains a major challenge that limits their widespread use. The influence of the LPSO phase on the corrosion behavior of these alloys is substantial. On one hand, the microgalvanic effect between the LPSO phase and α-Mg matrix can accelerate corrosion. On the other hand, the LPSO phase may serve as an effective barrier that hinders the spread of corrosion in as-cast Mg alloys. Although the distribution of the LPSO phases considerably influences the corrosion resistance, the relationship between the LPSO phase content and the corrosion resistance remains poorly understood. In this work, a series of as-extruded Mg-xY-yZn-0.1Mn (x = 2, 4, and 8, mass fraction, %; x / y = 2) alloys with varying LPSO contents and morphologies were prepared, and their corrosion resistance were investigated in detail. Microstructural analyses were conducted using OM, SEM, and XRD. Corrosion resistance was evaluated through hydrogen evolution, mass loss, and electrochemical testing. Corrosion morphologies were examined using OM, SEM, confocal laser scanning microscopy (CLSM), while the local corrosion potential was analyzed using scanning Kelvin probe force microscopy (SKPFM). The results showed that the alloys primarily consisted of α-Mg and LPSO phases. The volume fraction of LPSO increased with the elevation of Zn and Y contents, and the morphology of the LPSO phases varied among the alloys. In the Mg-2Y-1Zn-0.1Mn (WZ21M) alloy, which exhibited the lowest Zn and Y contents, the LPSO phases appeared as small blocks. In contrast, the Mg-4Y-2Zn-0.1Mn (WZ42M) alloy, with moderate Zn and Y contents, featured LPSO phases arranged zonally along the extrusion direction. The Mg-8Y-4Zn-0.1Mn (WZ84M) alloy, which exhibited the highest LPSO content, also exhibited a zonal distribution of LPSO phases but with a considerably reduced spacing between adjacent phases. Corrosion tests performed in a 3.5%NaCl (mass fraction) solution revealed that the corrosion resistance decreased in the following order: WZ84M < WZ42M < WZ21M. The WZ21M alloy, exhibited a smoother discharge process and a more negative discharge potential across different current densities, indicating higher corrosion resistance compared to the WZ42M and WZ84M alloys. Conversely, the WZ84M alloy, showed the poorest corrosion resistance due to the pronounced microgalvanic effect between the LPSO phase and α-Mg matrix. The deformed LPSO phases in the as-extruded alloy were less effective in inhibiting corrosion spread. The WZ21M alloy benefited from reduced microgalvanic effects, leading to improved corrosion resistance. Therefore, the corrosion resistance of as-extruded Mg-Y-Zn-Mn alloys is inversely related to the LPSO content, with higher LPSO contents generally resulting in decreased resistance due to intensified microgalvanic effects. Additionally, the morphology of the LPSO phase plays a critical role in determining corrosion resistance.

Key words:  Mg-Y-Zn alloy      LPSO phase      microstructure      corrosion resistance     
Received:  10 July 2024     
ZTFLH:  TG146.2  
Fund: National Natural Science Foundation of China(52171067);Natural Science Foundation of Guangdong Province(2024A1515030065);International Science and Technology Cooperation of Guangdong Science and Technology Plan Project(2023A0505050152);Basic and Applied Basic Research Project of Guangzhou(2024A04J6299);Young Talent Support Project of Guangzhou Association for Science and Technology(QT2024-012)
Corresponding Authors:  LI Chuanqiang, associate professor, Tel: 13060861457, E-mail: chuanqiang.li@gdut.edu.cn; WANG Desheng, senior engineer, Tel: 15038673657, E-mail: wangdesheng07@163.com

URL: 

https://www.ams.org.cn/EN/10.11900/0412.1961.2024.00230     OR     https://www.ams.org.cn/EN/Y2025/V61/I12/1803

Fig.1  Schematic of the testing surface of sample (ND—normal direction, TD—transverse direction, ED—extrusion direction)
Fig.2  XRD spectra of as-extruded Mg-2Y-1Zn-0.1Mn (WZ21M), Mg-4Y-2Zn-0.1Mn (WZ42M), and Mg-8Y-4Zn-0.1Mn (WZ84M) alloys (LPSO—long-period stacking ordered)
Fig.3  OM images of as-extruded WZ21M (a), WZ42M (b), and WZ84M (c) alloys
Fig.4  Low (a-c) and locally high (d-f) magnified SEM images of as-extruded WZ21M (a, d), WZ42M (b, e), and WZ84M (c, f) alloys
Fig.5  Hydrogen evolution rates (a) and mass loss rates (b) of as-extruded WZ21M, WZ42M, and WZ84M alloys exposed to 3.5%NaCl solution
Fig.6  Potentiodynamic polarization curves (a), Nyquist plots (b), Bode impedance plots (c), and Bode phase angle diagrams (d) of as-extruded WZ21M, WZ42M, and WZ84M alloys (E—potential, i—current density, Z″—imaginary part of impedance, Z′—real part of impedance, |Z|—impedance modulus. Inset in Fig.6c shows the equivalent circuit (Rssolution resistance; Rdl and CPEdl—charge transfer resistance and capacitance of the electrical double layer at the interface between substrate and electrolyte solution, respectively; Rfand CPEfresistance and capacitance of the corrosion products generated on the surface, respectively; RL—inductive resistance; L—inductance))
AlloyEcorr (vs SCE) / Vicorr / (μA·cm-2)
WZ21M-1.7126.49
WZ42M-1.6138.95
WZ84M-1.5845.60
Table 1  Tafel fitting results of as-extruded WZ21M, WZ42M, and WZ84M alloys derived from Fig.6a
Alloy

Rs

Ω·cm2

Rt

Ω·cm2

Ydl

μΩ-1·cm-2·sndl

ndl

Rf

Ω·cm2

Yf

μΩ-1·cm-2·snf

nf

RL

Ω·cm2

L

H·cm-2

WZ21M24.4606.013.400.93149.26200.30.872131.031598
WZ42M25.2511.218.050.93291.15076.90.871078.013511
WZ84M24.3459.416.140.94147.86509.70.812345.016867
Table 2  Fitted EIS data of as-extruded WZ21M, WZ42M, and WZ84M alloys
Fig.7  Discharge curves of as-extruded WZ21M, WZ42M, and WZ84M alloys under current densities of 2.5 mA/cm2 (a), 5 mA/cm2 (b), 10 mA/cm2 (c), and 20 mA/cm2 (d) (Vave—average voltage)
Fig.8  In situ OM images of the corrosion morphologies of as-extruded WZ21M (a1-a5), WZ42M (b1-b5), and WZ84M (c1-c5) alloys immersed in 3.5%NaCl solution for 1 h (a1-c1), 2 h (a2-c2), 4 h (a3-c3), 8 h (a4-c4), and 24 h (a5-c5)
Fig.9  Low (a-c) and locally high (d-f) magnified SEM images of as-extruded WZ21M (a, d), WZ42M (b, e), and WZ84M (c, f) alloys after immersion in 3.5%NaCl solution for 1 h and subsequently removing corrosion products
Fig.10  Low (a-c) and locally high (d-f) magnified SEM images of as-extruded WZ21M (a, d), WZ42M (b, e), and WZ84M (c, f) alloys after immersion in 3.5%NaCl solution for 24 h and subsequently removing corrosion products
Fig.11  3D corrosion morphologies of as-extruded WZ21M (a), WZ42M (b), and WZ84M (c) alloys after immersion in 3.5%NaCl solution for 24 h and subsequently removing corrosion products
Fig.12  Low (a-c) and locally high (d-f) magnified cross-sectional SEM images of as-extruded WZ21M (a, d), WZ42M (b, e), and WZ84M (c, f) alloys after immersion in 3.5%NaCl solution for 24 h and subsequently removing products
Fig.13  SKPFM testing results of as-extruded WZ21M, WZ42M, and WZ84M alloys
(a-c) potential distribution mappings of WZ21M (a), WZ42M (b), and WZ84M (c) alloys, respectively (d-f) line-profile analyses of relative voltage potential along the white lines in Figs.13a-c, respectively
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