This paper aimed to develop and characterize superhydrophobic surfaces with anticorrosive properties obtained by the chemical modification of the 5052 aluminum alloy with variation of acid etching time, formation of lamellar double hydroxides (LDH) film and immersion in stearic acid. The specimens were etched in HCl (2M) at 5, 10 and 30 min. The aluminum plates were treated with aqueous solution of zinc nitrate (0.1 M) in the presence of ammonia and then immersed in a stearic acid and ethanol solution (1% w/w) to reduce surface energy. Contact angles (CA) were determined. Surface morphology and composition were analyzed by scanning electron microscopy (SEM) and X-ray energy dispersion spectroscopy (EDS), respectively. Linear polarization tests were performed to analyze corrosion resistance. The optimal superhydrophobic performance was obtained with a contact angle of 154º for 30 min of acid etching. This condition also showed higher corrosion resistance, obtaining higher values of Ecorr and lower values of corrosion current density.

A variety of metallic components rely on properties that are specific to the alloy and its surface. Coatings have been extensively used to protect metallic surfaces from the aggressive effects of the environment to which it is exposed. In this investigation, the high temperature oxidation behavior of a FeCr and a FeCrY alloy coated with an aluminium based paint has been studied. The objective was to form the more resistant alumina surface layer on an aluminium free alloy. Aluminium based paint coated and uncoated specimens of the two alloys were oxidized for up to 200 hours at 1000 °C in air. The oxidized specimens were examined in a scanning electron microscope coupled to an energy dispersive system and the surfaces were analyzed by X ray diffraction analysis. The aluminium based paint coating increased the oxidation resistance of the alloys, mainly over extended periods. The FeCrY alloy coated with the Al based paint exhibited the highest oxidation resistance.

AISI 304L stainless steel powder compacts containing 2 vol% high purity rare earth oxides were prepared by mixing the different powders in a vibratory mill followed by pressing. The compacts thus obtained were sintered in a vacuum furnace and isothermal oxidation measurements were carried out in a muffle furnace, in air, up to 200 hours at 900 °C. The oxidized surfaces were examined in a scanning electron microscope and micro regions of the reaction products were studied using energy dispersive analysis. The addition of rare earth oxides decreased the oxidation rate of the stainless steel. Further evidence of predominant oxygen ion diffusion controlling the overall oxidation process in rare earth containing chromium oxide forming alloys has been observed.