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Corrosion and passivation

Most corrosion-resistant metals are protected by an invisible oxide film. Cleaning either preserves that film or breaks it, and breaking it is how stainless steel rusts.

In detail

Several metals that behave as though they are unreactive are in fact highly reactive metals carrying a protective skin. Aluminium and stainless steel both form a thin surface oxide within moments of exposure to air, and that passive film — not the bulk metal — is what resists corrosion. The film is self-repairing while oxygen is available, which is why a scratch in stainless steel does not usually lead to rust. Two things defeat it. Chloride ions can break the passive film down at localised points, producing pitting corrosion: small deep pits rather than general rusting, which is why chloride-containing residues such as bleach or salt left in contact with stainless steel are a genuine risk. And strong alkalis dissolve the oxide on aluminium outright, since aluminium oxide is amphoteric, exposing the reactive metal beneath. Both mechanisms share a practical conclusion: what matters is not only which cleaner is used but how completely it is removed afterwards.

Why

Sources for this page

Sources

  1. ASTM A967/A967M, Standard Specification for Chemical Passivation Treatments for Stainless Steel Parts

    ASTM International · Standards body

    Relied on for: That passivation produces a chromium-rich protective oxide film on stainless steel.

    Verification: the work exists and is described correctly. Nobody has yet read the specific passage.

  2. Kirk-Othmer Encyclopedia of Chemical Technology

    John Wiley & Sons · Reference work

    Relied on for: That chloride ions promote localised breakdown of passive films leading to pitting corrosion, and that aluminium oxide is amphoteric.

    Verification: the work exists and is described correctly. Nobody has yet read the specific passage.

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