Abstract
Anodic oxidation of an AZ91D magnesium alloy was carried out in an attempt to increase the corrosion resistance. The alloy was placed in an electrolyte containing 0.1 M sodium silicate (Na2SiO3), 2.0 m sodium hydroxide (NaOH) and 0.1 m sodium phosphate (Na3PO4), and treated with a current density of 100-400 mA/cm2 for 1 to 4 min. After the anodic oxidation treatment, the surface characteristics were analyzed by SEM, X-ray diffraction (XRD) and a surface roughness tester. The corrosion resistance was determined by measuring the corrosion potential and corrosion current density using potentiodynamic polarization in a 3.5 wt% NaCI electrolyte solution. Although the anodic oxidation treatment with the base electrolyte resulted in an arrival voltage ranging from 60 to 70 V, the addition of silicate tended to reduce this arrival voltage by approximately 10-20 V and decrease the critical voltage required for the formation of a porous oxide film. The pore size and film thickness increased with increasing applied current and treatment time. The addition of silicate to the electrolyte resulted in films with a homogeneous pore size and a film thickness increasing with the increasing applied current and treatment time. XRD showed the formation of a new MgO and Mg2Si04 phase. The formation of Mg2 SiO 4 was attributed to the presence of SiO44- in the film. After the addition of silicate, the corrosion potential increased and corrosion current decreased, resulting in improved corrosion resistance.
| Original language | English |
|---|---|
| Pages (from-to) | 1270-1277 |
| Number of pages | 8 |
| Journal | Surface and Interface Analysis |
| Volume | 40 |
| Issue number | 9 |
| DOIs | |
| State | Published - 2008.09 |
Keywords
- Anodic oxidation
- AZ91D magnesium alloy
- Oxide layer
- Sodium silicate
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