Magnesium and its alloys are widely used in many areas because of their light weight, excellent dimensional stability, and high strength-to-weight ratio. However, the material exhibits poor wear and corrosion resistance, which limits its use. Plasma electrolytic oxidation (PEO) is an effective surface modification method for producing ceramic oxide layers on Mg and their alloys. The influence of the additions of sodium tetrafluoroborate (NaBF₄) and sodium fluoride (NaF) into alkaline-silicate electrolyte on the properties of the conversion layers formed in the magnesium AZ91D alloy has been investigated. Surface morphology and chemical composition were determined by scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS). The anticorrosive properties of the layers were evaluated by electrochemical impedance spectroscopy (EIS) and potentiodynamic polarization (PDP) methods in simulated body fluid (SBF). The presence of NaBF₄ or NaF in the electrolyte increases the corrosion resistance of the protective layer. However, the best anticorrosive properties show the layers obtained in the presence of NaBF₄. This is probably caused by the incorporation of boron and fluorine in the form of Mg (BF₄)₂ mainly in the barrier layer.

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In this study, conversion coatings were produced on the AM50 magnesium alloy by a plasma electrolytic oxidation (PEO) process in alkaline-silicate electrolyte with the addition of potassium hexafluorophosphate, using a unipolar pulse power source. The coating microstructure and its composition were determined using scanning electron microscopy (SEM) and an X-ray photoelectron spectroscopy (XPS). The corrosion resistance of the conversion coatings was evaluated by means of potentiodynamic polarization tests (PDP) and electrochemical impedance spectroscopy (EIS) in a dilute Harrison solution (DHS). It has been found that the properties (microstructure, composition, and coating thickness) of the obtained layer and, therefore, their anticorrosive resistance strongly depend on the electrolyte composition. The best anticorrosive properties were observed in the layers obtained in the presence of 2.5 g/L KPF₆. It was found that the conversion coating produced with the addition of hexafluorophosphate is characterized by a different morphology (sponge-like) and better anticorrosion properties, in comparison to the coating obtained with the addition of fluoride and orthophosphate salts commonly used in PEO synthesis. The sponge-like structure, which is similar to bone structure in combination with the presence of phosphates in the layer, can increase the biocompatibility and the possibility of self-healing of this coating. However, neither Mg(PF₆)₂, nor any other compounds containing PF₆⁻, have been found in the layers produced.

Magnesium alloys, because of their excellent strength-to-weight ratio, are increasingly used in many industries. When used in external elements, the key factor is to provide adequate anticorrosion protection. High-temperature, cured-powder coatings are widely used to protect most metals, but their use on magnesium alloys is difficult as a result of the instability of the magnesium substrate at elevated temperatures. Another problem is ensuring the proper adhesion of the organic coating to the magnesium substrate. This paper presents the procedure for the synthesis of a duplex coating on AZ91 magnesium alloy. The topcoat was a powder coating based on acrylic resin, the main ingredient of which was glycidyl methacrylate. Because of the presence of epoxy groups, the coating was cured using ultraviolet (UV) radiation (low-temperature technology). The conversion subcoating was produced by plasma electrolytic oxidation (PEO) in an alkaline silicate electrolyte. The synthesized coating system was tested, among others, for microscopic (SEM), adhesive (mesh of cuts), and anticorrosion (EIS). The duplex PEO/UV-curable powder coating showed very good adhesion to the metal and increased the anticorrosion properties of the magnesium substrate, compared to the powder coating produced directly on the magnesium alloy and on an alternative conversion coating (synthesized in the process of chemical zircon phosphating).