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Full Length Article | Open Access

Mechanistic switch in corrosion behavior of magnesium alloy diamond lattice structures induced by argon plasma treatment

Viviana M. Posadaa,b,c,i( )Alexandru Marina,g,h( )Tonny Naranjod,eJuan Ramírezb( )Patricia Fernández-Moralesf
Ken and Mary Alice Lindquist Department of Nuclear Engineering, Pennsylvania State University, PA USA
Department of Mechanical Engineering, School of Mines, Universidad Nacional de Colombia, Bogotá, Colombia
Department of Nuclear, Plasma and Radiological Engineering, College of Engineering, University of Illinois at Urbana-Champaign, IL, USA
Medicine Faculty, Universidad Pontificia Bolivariana, Antioquia, Colombia
Corporación para Investigaciones Biológicas, Antioquia, Colombia
Industrial Engineering Faculty, Universidad Pontificia Bolivariana, Antioquia, Colombia
Materials Science and Engineering Department, Pennsylvania State University, University Park, PA, 16802, USA
Surface Analysis Laboratory, Institute for Nuclear Research Pitesti, Mioveni, 15400, Romania
Department of Electronics and Computer Science, Pontificia Universidad Javeriana de Cali, Colombia
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Abstract

Advancing 3D magnesium (Mg) development beyond current limitations requires controlling Mg alloy degradation in pre-designed, low-dimension architectures. This study reveals a mechanistic switch in the corrosion behavior of Mg alloy (3.6% Al, 0.8% Zn) diamond lattice structures, induced by plasma nanosynthesis (400 eV Ar+ ions, fluence 1 × 1017 ions/cm2). Plasma treatment of the Mg alloy increases surface Mg from 1.5% to 14.5%, enhances carbonate formation, and generates a nanostructured surface with a Mg carbonate layer over an oxide/hydroxide layer. In vitro and in vivo analyses over 8 wk demonstrate how this treatment fundamentally alters the degradation process and stability of these 3D architectures.

While untreated samples initially formed a protective film that subsequently diminished, DPNS-treated samples demonstrated an inverse corrosion behavior. X-ray photoelectron spectroscopy (XPS) and electrochemical impedance spectroscopy (EIS) confirmed the presence of a stable, protective layer composed of magnesium oxide, magnesium hydroxide, and magnesium carbonate on the DPNS-treated surfaces. After 14 days, the DPNS-treated sample exhibited a more positive corrosion potential (-0.69 V versus -1.36 V) and a marginally lower current density (0.73 mA/cm2 compared to 0.75 mA/cm2) relative to the control. This protective layer, combined with modified surface topology, initiated a core-to-periphery degradation pattern that maintained structural integrity for up to 8 wk post-implantation. These findings support the conclusion that the DPNS-treated scaffold demonstrates sustained improved corrosion resistance over time compared to the untreated control.

Micro-CT revealed plasma-treated samples retained larger struts (504.9 ± 95.3 µm at 8 wk) and formed larger H2 pockets extending 14.2 mm from the implant center, versus 4.9 mm in controls. This corrosion behavior switch enhances stability but risks pore clogging, offering insights for tailoring Mg alloy degradation and H2 evolution in 3D architectures for biomedical applications.

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Journal of Magnesium and Alloys
Pages 101-119

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Cite this article:
Posada VM, Marin A, Naranjo T, et al. Mechanistic switch in corrosion behavior of magnesium alloy diamond lattice structures induced by argon plasma treatment. Journal of Magnesium and Alloys, 2025, 13(1): 101-119. https://doi.org/10.1016/j.jma.2024.12.021

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Received: 01 August 2024
Revised: 16 December 2024
Accepted: 22 December 2024
Published: 14 January 2025
© 2025 Chongqing University

This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/) Peer review under responsibility of Chongqing University