A comparative study on the passivation and localized corrosion of α, β, and α + β brass in borate buffer solutions containing sodium chloride : I. Electrochemical data

The passivation and localized corrosion of α-, β-, and (α + β)-brass in borate-boric acid buffer solutions (pH 9) containing different NaCl concentrations (c<sub>NaCl</sub>) were studied comparatively using conventional electrochemical techniques at 25 °C. The passivation of brass in bor...

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Detalles Bibliográficos
Autores: Morales, Jose Carlos, Fernández, Guillermina T., Esparza, Pedro, González, Sergio G., Salvarezza, Roberto Carlos, Arvia, Alejandro Jorge
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:1995
País:Argentina
Institución:Universidad Nacional de La Plata
Repositorio:SEDICI (UNLP)
Idioma:inglés
OAI Identifier:oai:sedici.unlp.edu.ar:10915/80404
Acceso en línea:http://sedici.unlp.edu.ar/handle/10915/80404
Access Level:acceso abierto
Palabra clave:Ciencias Exactas
Química
Boratos
Cloruro de Sodio
Electroquímica
Corrosión
Boricum Acidum
Ácidos Bóricos
Técnicas Electroquímicas
Descripción
Sumario:The passivation and localized corrosion of α-, β-, and (α + β)-brass in borate-boric acid buffer solutions (pH 9) containing different NaCl concentrations (c<sub>NaCl</sub>) were studied comparatively using conventional electrochemical techniques at 25 °C. The passivation of brass in borate-boric acid buffer was due to the electroformation of a complex passive layer consisting of ZnO · xH<sub>2</sub>O and Cu<sub>2</sub>O—CuO. In NaCl-containing borate-boric acid buffer the breakdown of the passive layer occurs leading to pitting corrosion when the applied potential exceeds a certain critical value, E<sub>b</sub>. For a given type of brass, the value of E<sub>b</sub> is shifted negatively as c<sub>NaCl</sub> is increased. At a constant c<sub>NaCl</sub> the localized corrosion resistance of brass increases in the following order (α + β)-brass ≅ β-brass < α-brass. For all brass the localized corrosion resistance was lower than that of polycrystalline Cu, but considerably greater than that of polycrystalline Zn. Passive film composition and de-alloying can account for the localized corrosion resistance of these alloys.