High entropy alloys are a newly developed class of alloys, which tend to form a single solid solution or a mixture of solid solutions with simple crystal structures. These alloys possess excellent mechanical properties, thermal stability and corrosion resistance. In the present paper, an AlCoCrFeNiTi high entropy alloy was obtained by induction melting, and the influence of the remelting process on the mechanical and corrosion resistance characteristics of the alloy was investigated. Thus, optical and scanning electron microscopy revealed less phase segregation and a fine dendritic structure for the remelted alloy, while corrosion tests indicated that present alloy, in remelted state, has better corrosion resistance than as cast alloy and stainless steel. The Vickers microhardness measurements demonstrated an improvement of the alloy microhardness by remelting process due to the decrease in phase segregation and the increase in dendrite refinement level.
Potentiostatic electrodeposition was used to obtain CoCrFeMnNi high-entropy alloy (HEA) thin films on copper substrate. An electrolyte based on a DMSO (dimethyl sulfoxide)-CH3CN (acetonitrile) organic compound was used for the HEA deposition. The microstructure of the high-entropy deposits before and after corrosion in artificial seawater was investigated by scanning electron microscopy (SEM) and energy dispersive spectrometry (EDS) investigation. SEM analysis revealed that compact and uniform film consists of compact and uniform 50 nm–5 μm particles that form the HEA films. The successful co-deposition of all five elements was highlighted by the energy dispersive spectrometry investigation (EDS). Electrochemical measurements carried out in an aerated artificial seawater solution under ambient conditions demonstrated the promising potential for application in the field of anti-corrosion protection, due to the protective behavior of the HEA thin films.
In this paper, we investigate what effects heat treatment can have on potentiodynamically electrodeposited high-entropy thin film (HEA) CoCrFeMnNi alloys. We focused our study on the corrosion resistance in synthetic seawater, corroborated with the structure and microstructure of these thin films. Thin films of HEA alloys were deposited on a copper foil substrate, using an electrolyte based on the organic system dimethyl-sulfoxide (DMSO-(CH3)2SO)-acetonitrile (AN-CH3CN) (in a volume ratio of 4:1), which contains LiClO4 as electrolyte support and chloride salts of CoCl2, CrCl3 × 6H2O, FeCl2 × 4H2O, MnCl2 × 4H2O and NiCl2 × 6H2O. Using MatCalc PC software, based on the CALPHAD method, the structure and characteristics of the HEA system were investigated, and thermodynamic and kinetic criteria were calculated. The modeling process generated in the body-centered-cubic (BCC) or face-centered-cubic (FCC) structures a series of optimal compositions that are appropriate to be used in anticorrosive and tribological applications in a marine environment. Electrochemical measurements were carried out in an aerated artificial seawater solution at ambient temperature. In the experimental media, HEA thin films proved to have good corrosion resistance and were even better than the copper substrate. Corrosion resistance was improved after heat treatment, as shown by polarization and EIS tests. The structure and microstructure of HEA thin films before and after corrosion in artificial seawater were investigated by X-ray diffraction (XRD), scanning electron microscopy (SEM) and energy dispersive spectrometry (EDS). The XRD data showed no significant changes in the structure of HEA heat-treated thin films after the corrosion in saline media. The data obtained by polarization and ESI are supported by results from SEM-EDS. This complex study reveals that, for HEA thin films, heat treatment leads to an increase in corrosion resistance. So, this finding suggests that thermal annealing is an appropriate method for improving the corrosion performance of HEA thin films.
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