Corrosion resistance of in-situ growth of nano-sized Mg（OH）2 on micro-arc oxidized magnesium alloy AZ31—Influence of EDTA

One of the major obstacles for the clinical use of biodegradable magnesium(Mg)-based materials is their high corrosion rate. Micro-arc oxidation(MAO) coatings on Mg alloys provide mild corrosion protection owing to their porous structure. Hence, in this study a dense Mg(OH)2 film was fabricated on MAO-coated Mg alloy AZ31 in an alkaline electrolyte containing ethylenediamine tetraacetic acid disodium(EDTA-2 Na) to reinforce the protection. Surface morphology, chemical composition and growth process of the MAO/Mg(OH)2 hybrid coating were examined using field-emission scanning electron microscopy, energy dispersive X-ray spectrometer, X-ray diffraction, X-ray photoelectron spectroscopy and Fourier transform infrared spectrophotometer. Corrosion resistance of the coatings was evaluated via potentiodynamic polarization curves and hydrogen evolution tests. Results manifested that the Mg(OH)2 coating possesses a porous nano-sized structure and completely seals the micro-pores and micro-cracks of the MAO coating.The intermetallic compound of AlMn phase in the substrate plays a key role in the growth of Mg(OH)2 film. The current density of Mg(OH)2-MAO composite coating decreases three orders of magnitude in comparison with that of bare substrate, indicating excellent corrosion resistance. The Mg(OH)2-MAO composite coating is beneficial to the formation of calcium phosphate corrosion products on the surface of Mg alloy AZ31, demonstrating a great promise for orthopaedic applications.

Corrosion resistance of nanostructured magnesium hydroxide coating on magnesium alloy AZ31: influence of EDTA

A hexagonal nanosheet Mg(OH)2 coating was prepared through a one-step hydrothermal method using LiOH solution as mineralizer and then modified by ethylenediaminetetraacetic acid(EDTA) to minimize the rapid corrosion of AZ31 Mg alloy.The performance of the coating was evaluated using electrochemical technique,hydrogen evolution measurements, nanoscratch test,Fourier-transform infrared spectroscopy(FTIR), X-ray diffraction(XRD) patterns and field-emission scanning electron microscopy(FESEM).The results suggested that the corrosion rate of bare AZ31 Mg alloys was significantly reduced by one and two orders of magnitude through the protection from Mg(OH)2 coating and modification with EDTA(i.e., EDTA-Mg(OH)2 coating), respectively.FESEM micrographs indicated that the modification in EDTA elicits to the formation of an EDTA-Mg(OH)2 composite with a thickness as twice as that of as-prepared Mg(OH)2 coating.Nanoscratch tests revealed strong adhesion between the composite or Mg(OH)2 coating and the substrate.The study of formation and corrosion mechanisms of the coatings manifested that Mg(OH)2 was first formed near the intermetallic compound AlMn particles and gradually covered the entire surface, wherein the AlMn particles played an important role in the coating growth process.And it also proved that EDTA accelerated the formation of Mg(OH)2.

Biodegradation behavior of micro-arc oxidation coating on magnesium alloy-from a protein perspective

Protein exerts a critical influence on the degradation behavior of absorbable magnesium(Mg)-based implants.However,the interaction mechanism between protein and a micro-arc oxidation(MAO)coating on Mg alloys remains unclear.Hereby,a MAO coating was fabricated on AZ31 Mg alloy.And its degradation behavior in phosphate buffer saline(PBS)containing bovine serum albumin(BSA)was investigated and compared with that of the uncoated alloy.Surface morphologies and chemical compositions were studied using Field-emission scanning electron microscope(FE-SEM),Fourier transform infrared spectrophotometer(FT-IR)and X-ray diffraction(XRD).The degradation behavior of the bare Mg alloy and its MAO coating was studied through electrochemical and hydrogen evolution tests.Cytotoxicity assay was applied to evaluate the biocompatibility of Mg alloy substrate and MAO coating.Results indicated that the presence of BSA decreased the degradation rate of Mg alloy substrate because BSA(RCH(NH2)COO‾)molecules combined with Mg2+ions to form(RCH(NH2)COO)2Mg and thus inhibited the dissolution of Mg(OH)2 by impeding the attack of Cl‾ions.In the case of MAO coated Mg alloy,the adsorption of BSA on MAO coating and the formation of(RCH(NH2)COO)2Mg exhibited a synergistic effect and enhanced the corrosion resistance of the coated alloy significantly.Furthermore,cell bioactive assay suggested that the MAO coating had good viability for MG63 cells due to its high surface area.