Kinetics of the Fe+++/Fe++ Reaction on Fe-Cr Alloys

Abstract

The electrode kinetics of the Fe+++/Fe++ couple on passive Fe-Cr alloys were studied in acid solutions of constant ionic strength (M MgSO4). Tafel behavior is generally observed with exchange currents of the order of 10 to the -6th power amp/sq cm, a cathodic transfer coefficient of 0.40, and an anodic transfer coefficient of 0.36. The electrochemical reaction order is unity both for oxidation of Fe++ and reduction of Fe+++; the heat of activation at the reversible potential is 10.8 kcal/mol. The results show that an apprecible fraction (about 0.4) of the total potential drop on anodic polarization occurs within the passive film. This potential drop is probably associated with changes in the average oxidation state of cations between the inner and outer layer of the surface oxide. The electrochemical characteristics of the film depend on the pH of the solution, probably because of the migration of protons into the passive film. A change in the kinetics of Fe++ oxidation which occurs in the transpassive region for the Fe-Cr alloy is probably due to the production of Fe(+3) or Cr(+6) ions in the inner oxide layer.

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Document Details

Document Type
Technical Report
Publication Date
Jun 01, 1963
Accession Number
AD0411164

Entities

People

  • A. C. Makrides

Tags

Communities of Interest

  • Advanced Electronics
  • Air Platforms
  • Counter WMD
  • Weapons Technologies

DTIC Thesaurus Topics

  • Anodic Polarization
  • Chemical Reactions
  • Chemistry
  • Current Density
  • Electrochemical Reactions
  • Electrodes
  • Electrolytes
  • Ionic Current
  • Materials Science
  • Metals
  • Military Research
  • Oxidation
  • Oxidation Reduction Reactions
  • Oxides
  • Reaction Orders
  • Steady State
  • Temperature Coefficients

Fields of Study

  • Materials science

Readers

  • Electrochemical Engineering/ Fuel Cell Technologies