Lithium nitrate salt-assisted CO2 absorption for the formation of corrosion barrier layer on AZ91D magnesium alloy

Gyoung G. Jang, Jiheon Jun, Jong K. Keum, Yi Feng Su, Mayur Pole, Sridhar Niverty, Vineet V. Joshi

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Mg alloy corrosion susceptibility is a major issue that limits its wide industrial application in transport, energy and medical sectors. A corrosion-resistant layer containing crystalline MgCO3 was formed on the surface of AZ91D Mg alloy by Li salt loading and thermal CO2 treatment. Compared to the uncoated AZ91D surface, the surface layer exhibited up to a ∼15-fold increase in corrosion resistance according to the electrochemical results in 3.5 wt% NaCl solution and ∼32% decrease in wear rate compared to untreated AZ91D. The improved corrosion resistance is attributed to the formation of a <10 μm thick dense layer containing Mg, O, C and Li with crystalline MgCO3 phases. The initial step was to form a porous MgO layer on the surface of AZ91D Mg alloy, followed by loading an alkali metal salt (i.e., LiNO3) onto the MgO surface. The porous MgO surface was then reconstructed into a dense insulation layer containing Mg carbonate through CO2 absorption facilitated by molten Li salt during thermal CO2 treatment at 350 °C. As a potential method to utilize excessive CO2 for beneficial outcomes, the formation of the carbonate-containing film introduced in this study opens a new pathway for protecting various existing Mg alloys for diverse industrial applications.

Original languageEnglish
Pages (from-to)17696-17709
Number of pages14
JournalRSC Advances
Volume14
Issue number25
DOIs
StatePublished - Jun 3 2024

Funding

This work was supported by the US Department of Energy's (DOE's) Office of Energy Efficiency and Renewable Energy, Vehicle Technology Office, Lightweight Materials Core Program. Part of the materials characterization (SEM and in situ XRD) was performed at the Center for Nanophase Materials Sciences, which is sponsored at ORNL by DOE's Scientific User Facilities Division. This manuscript has been authored by UT-Battelle, LLC, under contract DE-AC05-00OR22725 with the US Department of Energy (DOE). The US government and the publisher, by accepting the article for publication, acknowledge that the US government retains a nonexclusive, paid-up, irrevocable, worldwide license to publish or reproduce the published form of this manuscript or allow others to do so for US government purposes. DOE will provide public access to these results of federally sponsored research in accordance with the DOE Public Access Plan (http://energy.gov/downloads/doe-public-access-plan).

FundersFunder number
U.S. Department of Energy
DOE Public Access Plan
US Government
Office of Energy Efficiency and Renewable EnergyDE-AC05-00OR22725

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