Effect of the Surface Film Formed by Hydrogen Charging on the Corrosion Behavior of an As-Cast Mg–8%Li (in wt. %) Alloy

Author:

Wang Shuo123,Xu Daokui245ORCID,Wang Baojie6,Wang Dongliang2,Zhang Zhiqiang13,Xu Xiangbo2

Affiliation:

1. Key Lab of Electromagnetic Processing of Materials, Ministry of Education, Northeastern University, Shenyang 110819, China

2. Key Laboratory of Nuclear Materials and Safety Assessment, Institute of Metal Research, Chinese Academy of Sciences, Shenyang 110016, China

3. Engineering Research Center of Advanced Materials Preparing Technology, Ministry of Education, Northeastern University, Shenyang 110819, China

4. Binzhou Institute of Technology, Binzhou 256606, China

5. Shandong Key Laboratory of Advanced Aluminium Materials and Technology, Binzhou 256606, China

6. School of Environmental and Chemical Engineering, Shenyang Ligong University, Shenyang 110159, China

Abstract

In this study, the effect of electrochemical hydrogen charging on the corrosion behavior of an as-cast Mg–8%Li alloy was investigated. It was revealed that after being cathodically hydrogen charged in a 0.1 M NaCl solution at a constant current density of 50 mA/cm2 for 3 h, a product film with an average thickness of 20 μm was formed in the α-Mg phase, whilst the average thickness of the product film being formed in the β-Li phase was 6 μm. When the charging time was prolonged to 18 h, the thicknesses of the product films being formed on the α-Mg and β-Li phases were increased to 75 and 20 μm, respectively. The results of the grazing incidence X-ray diffraction (GIXRD) testing showed that the product films of the differently charged samples mainly consisted of Mg(OH)2, LiOH and Li2CO3. The formed product films on the two matrix phases were dense and could hinder the erosion of Cl− in a solution, and hence improved the corrosion resistance of the alloy. After being hydrogen charged for 3 h, the charge-transfer resistance (Rct) value of the alloy was increased from 527 to 1219 Ω·cm2. However, when the hydrogen charging time was prolonged to 18 h, the Rct was slightly reduced to 1039 Ω·cm2 due to the cracking of the surface product films and the interfacial cracking of the film/substrate matrix.

Funder

National Natural Science Foundation of China

Liaoning Province’s project of “Revitalizing Liaoning Talents”

the Doctor Startup Fund of the Natural Science Foundation Program of Liaoning Province

the Strategic New Industry Development Special Foundation of Shenzhen

International Joint Laboratory for Light Alloys

the National Key Research and Development Program of China

the Innovation Fund of the Institute of Metal Research

the Fundamental Research Fund for the Central Universities

Bintech-IMR R&D Program

Publisher

MDPI AG

Subject

Materials Chemistry,Surfaces, Coatings and Films,Surfaces and Interfaces

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