REJANE MARIA PEREIRA DA SILVA

REJANE MARIA PEREIRA DA SILVA

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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).
O processo de anodização do alumínio e suas ligas
2021 - ARAUJO, JOAO V. de S.; SILVA, REJANE M.P. da; KLUMPP, RAFAEL E.; COSTA, ISOLDA
Al and its alloys are found in several industrial applications. However, like most metals, this material is not immune to corrosion, being necessary to be protected against corrosion. One of the methods most commonly employed to improve the corrosion resistance of Al alloys is the anodizing process, which consists of thickening of the natural oxide (Al2O3) presents in Al through anodic oxidation. The anodizing process is accomplished by immersion of the Al alloy into an acid bath and passing an electric current through it. This process produces two layers: a barrier layer thicker than the natural oxide and a layer with regular arrangement of nanopores (porous layer). This duplex structure forms the anodized layer with a large specific surface area. With the advent of nanotechnology, this layer has been applied in other areas due to its low cost, stability, absence of toxicity, and biocompatibility. In this context, this paper addresses a historical and electrochemical review of the anodizing process of Al and its alloys, presenting the main events that culminated in the development of the current processes and the understanding of the relationship between the chemical reactions and the mechanisms that occur during nucleation and development of the oxide layer.
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).
Microstructural, electrochemical and localized corrosion characterization of the AA2198-T851 alloy
2020 - ARAUJO, JOAO V. de S.; SILVA, REJANE M.P. da; DONATUS, UYIME; MACHADO, CARULINE de S.C.; COSTA, ISOLDA
In the present work, the microstructure, electrochemical behavior and localized corrosion of the AA2198-T851 Al-Cu-Li alloy were studied. The microstructure was correlated with corrosion results obtained by immersion, gel visualization and scanning electrochemical microscopy (SECM) tests. Immersion and gel visualization tests showed high kinetics of corrosion attack during the first hours of immersion. SECM analyzes by means of surface generation/tip collection (SG/TC) mode detected hydrogen evolution generated during spontaneous corrosion from severe localized corrosion (SLC) sites on the metal surface. SECM results revealed sites of intense hydrogen evolution after 2 h of immersion and increased amounts of corrosion products after 4 h of immersion. Hydrogen evolution sites detected by SECM were associated with severe localized corrosion (SLC).
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.