CATHODIC BEHAVIOUR of ANODIZED TITANIUM IN SIMULATED PHYSIOLOGICAL CONDITIONS

In the present work, anodic oxide films on titanium specimens were formed in physiological solution under potentiostatic condition. The immediate- to short-term changes in the oxide film were studied by open-circuit potential measurements and cyclic voltammetry. The results show that the intensity o...

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Detalles Bibliográficos
Autores: Pelaez Abellan, E., Rocha-Sousa, L., Guastaldi, Antonio Carlos [UNESP]
Tipo de recurso: artículo
Estado:Versión publicada
Fecha de publicación:2011
País:Brasil
Institución:Universidade Estadual Paulista (UNESP)
Repositorio:Repositório Institucional da UNESP
Idioma:inglés
OAI Identifier:oai:repositorio.unesp.br:11449/41487
Acceso en línea:http://www.scielo.org.ar/scielo.php?script=sci_arttext&pid=S0327-07932011000300001&lng=pt&nrm=iso&tlng=en
http://hdl.handle.net/11449/41487
Access Level:acceso abierto
Palabra clave:Cathodic Behaviour
Cyclic Voltammetry
Anodized Titanium
Titanium Oxide
Descripción
Sumario:In the present work, anodic oxide films on titanium specimens were formed in physiological solution under potentiostatic condition. The immediate- to short-term changes in the oxide film were studied by open-circuit potential measurements and cyclic voltammetry. The results show that the intensity of the cathodic current peak related to oxygen reduction at around -0.7 Vsce, decreased and disappeared after 30 minutes of finishing the anodic oxidation. For titanium without anodization (non-coated titanium), the cyclic voltammograms show an anodic current in the range that begins at -0.9 Vsce and continues to more positive potentials (vs SCE), related to the hydrogen oxidation reaction. For anodically polarized titanium (coated titanium), in the anodic direction of the cyclic voltammograms an anodic current in the range that begins at -0.9 Vsce and continues to more positive potentials (vs SCE) was observed. In this case, the oxidation process is related to previous cathodic processes: the hydrogen formation and the cathodic transformation of titanium oxides before the oxygen reduction potential region.