Marie-Georges Olivier

Magnesium alloys are promising candidates for biomedical implants, but their rapid corrosion limits clinical use. Simulated body fluid (SBF) is commonly used to evaluate corrosion behaviour; however, Ca-P and carbonate deposits can mask the intrinsic performance of protective coatings. Tris(hydroxymethyl)aminomethane (Tris) has been proposed as an SBF modifier, although its effect on coated magnesium remains poorly understood. While Tris modifies the buffering characteristics of the solution, it also alters the stability of Mg(OH)₂ and the precipitation equilibria of corrosion products, resulting in more aggressive corrosion conditions than standard SBF. Here, the corrosion behaviour of AZ31 alloy, a plasma electrolytic oxidation (PEO) coating, and a sol-gel sealed PEO coating was investigated in SBF with and without Tris. Electrochemical impedance spectroscopy, immersion tests, pH monitoring, and post-immersion SEM/EDS analyses were used to evaluate coating performance under physiological and aggressive conditions. The results show that AZ31 and PEO coatings exhibit higher apparent corrosion resistance in SBF without Tris due to corrosion-product stabilization and Ca-P-rich deposits that partially block electrolyte access. In contrast, SBF with Tris accelerates degradation, causing uniform corrosion of AZ31 and premature PEO failure through electrolyte penetration and coating cracking. The PEO-AR/ZTP system maintains the highest electrochemical resistance and the best protective performance in both media.

ZnAl and ZnAlCe layered double hydroxide (LDH) conversion layers modified with picolinoyl N4-phenylthiosemicarbazide (HL) are fabricated on hot-dip galvanized steel (HDG) to improve corrosion protection. X-ray diffraction (XRD) confirms that HL molecules are not intercalated within the LDH interlayers, whereas Fourier transform infrared spectroscopy (FT-IR), X-ray photoelectron spectroscopy (XPS), and energy-dispersive X-ray spectroscopy (EDS) analyses reveal their surface adsorption. Moreover, scanning electron microscopy (FE-SEM) observations reveal that HL modification induces changes in surface morphology. After 168 h in 0.1 M NaCl, the LDH structure remains intact, and N and S signals are still detected, confirming the persistence of both the LDH layer and adsorbed HL molecules under corrosive conditions. During 168 h immersion in NaCl, electrochemical measurements indicate that the modified LDH layers exhibit higher corrosion resistance than the unmodified ones, with the ZnAlCe LDH/HL coating providing the most effective protection.

This study aims to investigate the effects of different fluoride salts added in the PEO bath on the corrosion resistance and morphology of AZ31 magnesium alloy coatings. The PEO process was performed using a bipolar cycle with varying durations (4 and 30 min) in baths containing different fluoride salts (NaF, LiF, Na₂SiF₆) and a reference bath without fluoride. The coatings were characterised using SEM-EDS, XRD, and electrochemical impedance spectroscopy (EIS) to assess their morphology, chemical composition, and corrosion resistance. The results indicate that the presence of fluorides significantly influences the coating properties. NaF and Na₂SiF₆ coatings exhibited better corrosion resistance and more compact microstructures compared to LiF and the fluoride-free reference. The study highlights the importance of the fluoride counter ion in the PEO bath, demonstrating that NaF and Na₂SiF₆ provide superior protection against corrosion, making them suitable for biomedical applications where both porosity and corrosion resistance are critical.

Polybenzoxazine (PBz) resins exhibit excellent mechanical, thermal, and adhesive properties, making them interesting candidates for coating applications. Moreover, thanks to the incorporation of exchangeable ester bonds within the PBz network, the coating presents healable properties that are catalyzed by the intrinsic presence of tertiary amine within the PBz backbone. Unfortunately, these tertiary amine functions are also responsible for the limited resistance of such systems to acid environments by protonation. To address this limitation, the protection of tertiary amines inherent to the PBz network was investigated in this study by incorporating an aromatic group close to the amine function to minimize its protonation via hindrance/mesomeric effects. More precisely, benzoxazine precursors based on monoethanolamine (mea) and aminophenylethyl alcohol (Apa) were synthesized and tested as protective coatings of aluminium alloy substrates (AA1050). The resins were characterized by NMR, FTIR, rheology, TGA, DSC, and DMA. PBz synthesized from Apa exhibits enhanced thermal stability, reduced swelling rates in both water and acid, and shortened relaxation times. After application via solvent casting on AA1050 substrates, the acid resistance of the coatings was evaluated. Electrochemical impedance spectroscopy results demonstrated better resistance of the Apa-based resins in 0.1 M sulfuric acid after one month of immersion.

In recent years, there has been significant research and development in area of corrosion prevention and protection, focusing on hydrotalcites layers on zinc and zinc alloys due to their distinct attributes, such as their capability to accommodate anions, ability to exchange anions, capability for structural memory, and its resistance to barriers. This review primarily aims to summarize findings related to how the formation of HT layers on zinc and zinc alloys is affected by various synthesis conditions. Besides, we compared and deliberated upon HT layers' anti-corrosion mechanism and corrosion protection.

In this investigation, the sol–gel method is employed along with a corrosion inhibitor to seal a plasma electrolytic oxidation (PEO) coating, aiming to improve the long-term corrosion resistance of the AZ31 Mg alloy. Following an initial screening of corrosion inhibitors, 8-hydroxyquinoline (8HQ) is incorporated into the hybrid PEO/sol–gel system using two methods: (i) post-treatment of the PEO layer through immersion in an inhibitor-containing solution; (ii) loading the inhibitor into the sol–gel precursor. The characterization includes scanning electron microscopy (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), ultraviolet-visible spectroscopy (UV-vis), and water drop contact angle measurements. The rheological properties of the inhibitor-loaded sol–gel precursors are assessed by measuring flow curves. The corrosion processes are evaluated in a saline solution through electrochemical impedance spectroscopy (EIS) and immersion tests with unscratched and scratched specimens, respectively. The results demonstrate the successful incorporation of the inhibitor for both loading strategies. Regardless of the loading approach, systems containing 8HQ exhibit the most favourable long-term corrosion resistance.