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March 6, 2026Materials Letters0 citationsOpen Access

Initiation stage of Ti6Al4V corrosion in H2O2-containing phosphate buffer saline

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EME. MauriotFVF. VuckoPMP. Marmet

Key Points

  • The aim is to investigate the early dissolution of the β phase in Ti6Al4V in a hydrogen peroxide solution.
  • Ti6Al4V samples were exposed to 1 M H2O2 in phosphate buffer saline for 30 minutes.
  • Electrochemical impedance spectroscopy (EIS) was conducted to assess corrosion rates.
  • Scanning electron microscopy (SEM) and bright-field transmission electron microscopy (BF-TEM) were performed to observe surface changes.
  • Random dissolution of the β phase occurred after 30 minutes of exposure.
  • Hydrogen peroxide exposure caused defects up to 250 nm in size.
  • Galvanic coupling was observed between the α phase (cathodic) and β phase (anodic).
  • The identified defects are not expected to compromise the mechanical integrity of dental implants.

Abstract

α + β Ti6Al4V samples were exposed to a phosphate buffer saline (PBS) solution containing 1 M of H 2 O 2 for short durations (30 min) to investigate the initial stage of the β phase dissolution. Electrochemical impedance spectroscopy (EIS) measurements and post-mortem scanning electron microscopy (SEM) analysis of the samples revealed randomness in the initiation of β phase dissolution. Bright-field transmission electron microscopy (BF-TEM) imaging and scanning kelvin probe force microscopy (SKPFM) measurements suggested a galvanic coupling between the α and β phases. • Random β phase dissolution after 30-min exposure of Ti6Al4V surfaces to 1 M H 2 O 2 . • Galvanic coupling between cathodic α phase and anodic β phase. • Up to 250 nm defects may appear after 30-min exposure to H 2 O 2 . • Such defects are unlikely to affect mechanical integrity of a dental implant.

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Cite This Study

Mauriot et al. (2026) studied this question.

synapsesocial.com/papers/69aa6f3c531e4c4a9ff5955ehttps://doi.org/10.1016/j.matlet.2026.140379
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