Faraday paradox (electrochemistry)

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This article is about Faraday paradox in electrochemistry. For Faraday paradox in electromagnetism, see Faraday paradox.

The Faraday paradox was a once inexplicable aspect of the reaction between nitric acid and steel. Around 1830, the English scientist Michael Faraday found that diluted nitric acid would attack steel, but concentrated nitric acid would not.[1] The attempt to explain this discovery led to advances in electrochemistry.

Passivation[]

Faraday's electrochemical paradox arises from his famous iron in the nitric acid experiment of 1833. Concentrated nitric acid had been synthesized and although Faraday did not have a pH meter (the pH scale would not be developed for another seventy years), Faraday knew from various tests (e.g., taste and time of dissolution of calcite chips) that concentrated nitric acid was a much stronger acid than dilute nitric acid. Thus, when he placed the iron in the dilute acid gas (we now know to be hydrogen) was evolved from the surface and the iron dissolved. When he placed the iron in the concentrated nitric acid, he expected that it would dissolve at a higher rate but no attack was observed. He then scratched the surface and a burst of bubbles was generated but then ceased. He opined that the surface had become "passive" and he correctly surmised that the surface was oxidized and become covered with a protective oxide film. But, why did the oxide film not dissolve and the attack continue in the concentrated nitric acid? This became known as Faraday's electrochemical paradox, and was not resolved until 1989[2]

The key to resolving the paradox is passivation. When the acid is concentrated enough, and because concentrated nitric acid is an oxidizing agent, the potential of the metal is raised to the point that a layer of metastable Fe3O4 forms on the surface and protects it from further corrosion, even though the pH is so low that stable Fe3O4 cannot exist. This explanation is supported by the observation that scratching the surface causes a burst of bubbles. Diluted nitric acid is not as strong an oxidizing agent and hence does not raise the potential of the metal to the extent that metastable Fe3O4 forms on the surface. In this case, the metal freely corrodes.[3]

References[]

  1. ^ Digby D. Macdonald, Passivity - the key to our metals-based civilization, IUPAC 1999 (PDF here)
  2. ^ D. D. Macdonald and G. A. Cragnolino. “Corrosion and Erosion-Corrosion of Steam Cycle Materials”. Chapter 9 in Water Technology for Thermal Power Systems. Edited by P. Cohen. New York, NY. (1989). American Society of Mechanical Engineers.
  3. ^ Strong, Oxidizing acids at the National Oceanic and Atmospheric Administration
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