What Causes Stainless Steel to Rust?

Stainless steel is an iron-based alloy known for its superior resistance to corrosion, which is why it is used widely in applications from cookware to architecture. While standard steel rusts readily when iron reacts with oxygen and moisture to form iron oxide, stainless steel is not entirely immune to corrosion. The material is better described as corrosion-resistant, meaning it can still suffer damage under specific, aggressive conditions that overwhelm its built-in defenses.

The Passivation Layer

The corrosion resistance of stainless steel stems from a unique, self-forming surface defense mechanism called the passivation layer. Stainless steel must contain a minimum of 10.5% chromium, which forms this protection. When the steel surface is exposed to oxygen, the chromium atoms react spontaneously to form a microscopically thin layer of chromium oxide.

This film is tightly adherent, non-porous, and chemically stable, acting as an invisible barrier between the underlying metal and the environment. The concept of “passivity” means the steel has become chemically unreactive under normal conditions because this oxide film blocks the diffusion of oxygen and water to the iron atoms beneath.

The layer’s most remarkable property is its ability to self-repair, provided oxygen is present. If the surface is damaged, the exposed chromium immediately reacts with oxygen to regenerate the protective chromium oxide film. This continuous, dynamic capability is the primary defense system that keeps the steel “stainless.”

Specific Environmental Factors That Cause Breakdown

The protection offered by the passivation layer can be overwhelmed when the steel is exposed to specific external agents or conditions that compromise the film’s stability or prevent its self-repair. The most common and aggressive factor is the presence of chloride ions, such as those found in salt, seawater, or many common household cleaning products.

These small, highly mobile ions are capable of penetrating and chemically breaking down the chromium oxide film, especially at localized weak points on the surface. Once the layer is breached, the underlying iron is exposed, initiating a localized corrosion reaction.

Environments that restrict the flow of oxygen to the steel surface also pose a significant threat because they inhibit the layer’s ability to self-repair. In tight spaces, such as under gaskets, washers, or beneath accumulated dirt and deposits, the oxygen supply becomes depleted. Without sufficient oxygen, the passive film cannot regenerate after localized damage, allowing corrosion to progress unchecked in that specific area.

Another major cause of breakdown is surface contamination, particularly from carbon steel particles. This often occurs when stainless steel is fabricated or cleaned using tools previously used on ordinary steel, such as a wire brush or grinder. These embedded iron particles act as localized sites for conventional rusting, sometimes called “flash rust,” which then disrupts the surrounding passive layer and accelerates the damage.

Exposure to excessive heat can also destroy the protective mechanism. Exposure to temperatures typically between 450°C and 850°C (842°F and 1562°F) can cause sensitization. During sensitization, chromium combines with carbon within the steel to form chromium carbides along the grain boundaries. This depletes the chromium content near the surface, preventing the formation of a robust passive layer and making the steel highly susceptible to corrosion.

Common Forms of Stainless Steel Corrosion

When the passivation layer is compromised, the damage manifests as specific, localized forms of corrosion. The most frequent type of failure is pitting corrosion, primarily driven by the presence of chloride ions. This process begins when chlorides break down the passive film in a small, isolated spot, leading to the formation of a tiny pit that deepens rapidly into the metal. The corrosion product formed inside the pit accelerates the attack, making pitting an aggressive and difficult-to-detect form of localized damage.

Another common manifestation is crevice corrosion, which occurs in tight, stagnant spaces where oxygen is excluded. This form is typically found under bolt heads, washers, flanges, or deposits of dirt where the environment becomes chemically imbalanced. The lack of oxygen prevents the passive film from healing, while the localized chemistry within the crevice becomes more acidic and concentrated with aggressive ions, leading to rapid material loss confined to the gap.

A third distinct form is galvanic corrosion, which occurs when stainless steel is in electrical contact with a less noble metal. In the presence of an electrolyte, such as moisture, an electrical current flows between the two dissimilar metals. The less noble metal, like aluminum or carbon steel, becomes the anode and corrodes at an accelerated rate. The stainless steel itself can also be affected if the corrosive conditions are severe.