2019
DOI: 10.1016/j.jmrt.2019.09.023
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Corrosion behaviour of Ti6Al4V ELI nanotubes for biomedical applications

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Cited by 24 publications
(11 citation statements)
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“…The corrosion potential measured by potentiodynamic polarization has a lower value for anodized than bare Ti alloy. EIS results confirm that anodic anodization of Ti-6Al-4V ELI alloy permits the growth of a thick oxide compact layer at the base of the nanotubes array (see Scheme of Figure 8b), guaranteeing high corrosion resistance [131].…”
Section: Electrochemical Biocorrosion Of Passive Coatings On Ti-6al-4vmentioning
confidence: 52%
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“…The corrosion potential measured by potentiodynamic polarization has a lower value for anodized than bare Ti alloy. EIS results confirm that anodic anodization of Ti-6Al-4V ELI alloy permits the growth of a thick oxide compact layer at the base of the nanotubes array (see Scheme of Figure 8b), guaranteeing high corrosion resistance [131].…”
Section: Electrochemical Biocorrosion Of Passive Coatings On Ti-6al-4vmentioning
confidence: 52%
“…The corrosion potential measured by potentiodynamic polarization has a lower value for anodized than bare Ti alloy. EIS results confirm that anodic anodization of Ti-6Al-4V ELI alloy permits the growth of a thick oxide compact layer at the base of the nanotubes array (see Scheme of Figure 8b), guaranteeing high corrosion resistance [131]. The research trend to increase the corrosion resistance of Ti-6Al-4V alloy goes toward the fabrication of uniform and highly ordered nanoporous layer by anodic oxidation.…”
Section: Electrochemical Biocorrosion Of Passive Coatings On Ti-6al-4vmentioning
confidence: 56%
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“…The experimental results were fitted using the equivalent circuit C (Figure c). The element R el corresponds to the solution resistance, R 1 and Q 1 represent the charge transfer resistance and the constant phase element of the nanotube layer with and without cerium mixed oxide coating, while R 2 and Q 2 are related to the inner oxide layer . It was possible to employ the same equivalent circuit for nanotubular surfaces after cerium mixed oxide deposition because this outer layer did not occlude the nanotube system.…”
Section: Resultsmentioning
confidence: 99%
“…The element R el corresponds to the solution resistance, R 1 and Q 1 represent the charge transfer resistance and the constant phase element of the nanotube layer with and without cerium mixed oxide coating, while R 2 and Q 2 are related to the inner oxide layer. 33 It was possible to employ the same equivalent circuit for nanotubular surfaces after cerium mixed oxide deposition because this outer layer did not occlude the nanotube system. From the Nyquist spectra and the fit lines shown in Figure 4 (black and green lines), it can be observed that the samples (TiNT) without the presence of cerium oxide showed remarkable corrosion resistance, remaining unaffected in the presence of hydrogen peroxide in the SBF solution.…”
Section: Electrochemicalmentioning
confidence: 99%