MARIANA XAVIER MILAGRE

MARIANA XAVIER MILAGRE

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Investigação da atividade eletroquímica de liga Al-Cu-Li após processo de soldagem por fricção e mistura
2023 - SILVA, REJANE M.P. da; MILAGRE, MARIANA X.; ARAUJO, JOAO V. de S.; RAMIREZ, OSCAR M.P.; MACHADO, CARULINE de S.C.; ANTUNES, RENATO A.; COSTA, ISOLDA
In this work, the local electrochemical activity of the zones coupled by Friction Stir Welding (FSW) of an Al-Cu-Li alloy was studied and the results were correlated to the microstructural characteristics of each zone. Electrochemical studies were carried out in the zones affected by welding using cyclic voltammetry (CV) and scanning electrochemical techniques (namely, SECM - Scanning Electrochemical Microscopy and LEIS – Local electrochemical impedance spectroscopy). The results showed that the welding joint (WJ) is predominantly cathodic relatively to the heat affected zones (HAZ). The HAZ was always anodic and showed the highest electrochemical activities among the tested ones. The high electrochemical activity of the HAZ was associated with the effect of galvanic coupling between the cathodic region (WJ) and the anodic region (HAZ). In addition, the advancing side (AS) presented increased electrochemical activity compared to the retreating one (RS).
Compreendendo os mecanismos de corrosão de ligas de Al-Cu-Li
2022 - ARAUJO, JOAO V. de S.; SILVA, REJANE M.P. da; VIVEIROS, BARBARA V.; MILAGRE, MARIANA X.; MACHADO, CARULINE de S.C.; COSTA, ISOLDA
In this study, the corrosion mechanism of an Al-Cu-Li alloy manufactured by two different treatment routes (T3 and T851) was evaluated by immersion and electrochemical tests in solutions containing chloride ions (Cl-). For both alloys, the formation of cavities on the surface was associated with micrometer-sized intermetallics (IM’s), however, in addition to this attack, the alloy submitted to T851 treatment also presented an attack called severe localized corrosion (SLC), caused by the preferential attack to the nanometric T1 (Al2CuLi) phase. The electrochemical concepts involved in these two types of attacks were discussed. During the IM’s corrosive process, whereas the O2 reduction occurred over the IM’s, the Al dissolution is favored around the particle, forming trenching and cavities (with 2 and 6 mm of depth). On the other hand, the mechanism associated with the SLC is related to the formation of a differential aeration cell followed by the evolution of H2, with greater depth of attack penetration (8 and 35 mm). Additionally, by the use of the Scanning Vibrating Electrode Technique (SVET), it was concluded that the higher anodic currents observed for the T851 temper were related to the relation between the anodic area (Aa) and the cathodic area (Ac).
Corrosion protection of the AA2198-T8 alloy by environmentally friendly organic-inorganic sol-gel coating based on bis-1,2-(triethoxysilyl) ethane
2021 - KLUMPP, RAFAEL E.; DONATUS, UYIME; SILVA, REJANE M.P. da; ANTUNES, RENATO A.; MACHADO, CARULINE de S.C.; MILAGRE, MARIANA X.; ARAUJO, JOAO V. de S.; VIVEIROS, BARBARA V.G. de; COSTA, ISOLDA
In this work, a surface coating composed of organic‐inorganic hybrid sol‐gel based on bis‐1,2‐(triethoxysilyl) (BTSE) ethane was applied on AA2198‐T8 samples, and its effect on corrosion resistance was investigated and compared with that of a chromate layer formed in a solution with hexavalent chromium ions. The corrosion resistance of BTSE coated samples was evaluated by immersion tests in sodium chloride solution (0.005 mol/L NaCl) and monitored by global electrochemical techniques such as electrochemical impedance spectroscopy (EIS) and local electrochemical techniques such as scanning vibrating electrode technique (SVET) and scanning electrochemical microscopy (SECM). The formed coating layers were characterized by X‐ray photoelectron spectroscopy (XPS). The results pointed out that the BTSE is an effective alternative coating for corrosion protection of new generation Al‐Cu‐Li alloys and could replace chromates obtained in toxic and carcinogenic CrVI containing solutions leading to improved corrosion protection.
Mecanismo de evolução de hidrogênio durante a corrosão da liga 2198-T8 em meio contendo cloreto
2020 - ARAUJO, JOAO V. de S.; SILVA, REJANE M.P. da; MILAGRE, MARIANA X.; MACHADO, CARULINE de S.C.; COSTA, ISOLDA
Corrosion is still one of the most serious and frequent problems in industries. The phenomena involved in the corrosion mechanism of Al-alloys may be explained by formation of galvanic cells between the metal matrix and heterogeneities, such as precipitates, intermetallic phases leading to potential differences and electrochemical reactions. In the cathodic sites, the main reactions are oxygen reduction reaction, in aerated neutral environments, and hydrogen evolution in acid media. This last type of reaction might also occur in neutral solutions inside pits (anodic region). In this study, the mechanism of hydrogen evolution during corrosion of the 2198-T8 Al-Cu-Li alloy exposed in a chloride solution was investigated. The mechanism was related to the presence of T1 phase (Al2CuLi), which is the main strengthening phase in this material. This phase is highly active and, when exposed to corrosive media, leads to severe localized corrosion (SLC). One of the main characteristics related to SLC is hydrogen gas evolution which was confirmed by gel visualization. In this study, the hydrogen evolution mechanism inside the SLC sites was studied by scanning electrochemical microscopy (SECM).
The local electrochemical behavior of the AA2098‐T351 and surface preparation effects investigated by scanning electrochemical microscopy
2019 - SILVA, REJANE M.P. da; MILAGRE, MARIANA X.; OLIVEIRA, LEANDRO A. de; DONATUS, UYIME; ANTUNES, RENATO A.; COSTA, ISOLDA
In this work, scanning electrochemical microscopy (SECM) measurements were employed to characterize the electrochemical activities on polished and as‐received surfaces of the 2098‐T351 aluminum alloy (AA2098‐T351). The effects of the near surface deformed layer (NSDL) and its removal by polishing on the electrochemical activities of the alloy surface were evaluated and compared by the use of different modes of SECM. Confocal laser scanning microscopy (CLSM) and scanning electron microscopy (SEM) were also employed to characterize the morphology of the surfaces. The surface chemistry was analyzed by X‐ray photoelectron spectroscopy (XPS). The surface generation/tip collection (SG/TC) and competition modes of the SECM were used to study hydrogen gas (H2) evolution and oxygen reduction reactions, respectively. H2 evolution and oxygen reduction were more pronounced on the polished surfaces. The feedback mode of SECM was adopted to characterize the electrochemical activity of the polished surface that was previously corroded by immersion in a chloride‐containing solution, in order to investigate the influence of the products formed on the active/passive domains. The precorroded surface and as‐received surfaces revealed lower electrochemical activities compared with the polished surface showing that either the NSDL or corrosion products largely decreased the local electrochemical activities at the AA2098‐T351 surfaces.
Effect of surface treatments on the localized corrosion resistance of the AA2198‐T8 aluminum lithium alloy welded by FSW process
2019 - MACHADO, CARULINE de S.C.; KLUMPP, RAFAEL E.; AYUSSO, VICTOR H.; DONATUS, UYIME; MILAGRE, MARIANA X.; ARAUJO, JOAO V. de S.; MACHADO, GLAUSON A.F.; COSTA, ISOLDA
In this work, the effect of eight types of surface treatments on the corrosion resistance of friction stir welded samples of an AA2198‐T8 Al‐Cu‐Li alloy were tested and compared in an attempt to find suitable alternatives to toxic and carcinogenic hexavalent chromium treatments. All the samples were anodized and subjected to different post‐anodizing treatments. The post‐anodizing treatments were (1) hydrothermal treatment in Ce (NO3)3 6H2O solution; (2) hydrothermal treatment in Ce (NO3)3 6H2O solution with H2O2; (3) hydrothermal treatment in boiling water; (4) hexavalent chromium conversion coating; and (5) immersion in BTSE (bis‐1,2‐(triethoxysilyl) ethane. The corrosion resistance of the treated samples was evaluated by immersion tests in sodium chloride solution (0.1 mol L−1 NaCl) and electrochemical impedance spectroscopy (EIS) of the friction stir weldment. The results showed that among the alternative treatments, the Ce‐containing solutions presented the best corrosion resistance, especially when used without peroxide.
The effect of surface pretreatment on the corrosion behaviour of silanated AA2198‐T851 Al‐Cu‐Li alloy
2019 - DONATUS, UYIME; KLUMPP, RAFAEL E.; MOGILI, NAGA V.V.; ANTUNES, RENATO A.; MILAGRE, MARIANA X.; COSTA, ISOLDA
The corrosion behaviour of silanated AA2198‐T851 alloy substrates with and with no manufacturing‐process induced near‐surface deformed layer (MPI‐NSDL) has been investigated. Two methods (alkaline etching + desmutting and mechanical polishing) were employed in removing the MPI‐NSDL. Silanization was performed using 2‐bistriethoxysilylethane. Electrochemical impedance spectroscopy (EIS), salt spray test, and microscopy techniques were employed in the investigation of the corrosion behaviours. The studies revealed that polishing appeared to be the best silanating pre‐treatment (compared with degreasing and etching + desmutting) for the new generation AA2198‐T851 Al‐Cu‐Li alloy, and this was reflected in the EIS spectra. The etched + desmutted and the degreased surface with MPI‐NSDL did not respond well to silanization and presented more pitting sites per square millimeter. However, the severity of corrosion per pit was more on the polished sample compared with the other two. Also, the corrosion mechanisms were different for the three cases.