Passive Film Formation and Localized Corrosion

Passivating inhibitors act in two ways. First they can reduce the passivating current density by encouraging passive film formation, and second they raise the cathodic partial current density by their reduction. Inhibitors can have either both or only one of these properties. Passivating inhibitors belong to the group of so-called dangerous inhibitors because with incomplete inhibition, severe local active corrosion occurs. In this case, passivated cathodic surfaces are close to noninhibited anodic surfaces. 

If the passive film cannot be reestablished and active corrosion occurs, a potential drop is established in the occluded region equal to IR where R is the electrical resistance of the electrolyte and any salt film in the restricted region. The IR drop lowers the electrochemical potential at the metal interface in the pit relative to that of the passivated surface. Fluctuations in corrosion current and corrosion potential (electrochemical noise) prior to stable pit initiation indicates that critical local conditions determine whether a flaw in the film will propagate as a pit or repassivate. For stable pit propagation, conditions must be established at the local environment/metal interface that prevents passive film formation. That is, the potential at the metal interface must be forced lower than the passivating potential for the metal in the environment within the pit. Mechanisms of pit initiation and propagation based on these concepts are developed in more detail in the following section. 

The alloy composition (and microstructure) has strong effects on all the aspects of passivity that have been described above chemical composition and thickness of the passive film, electronic properties, structure, and kinetics of formation. The influence of alloyed elements on the electrochemical characteristics of passive systems can be seen in Fig. 3-16. This is the same current-potential curve as in Fig. 3-1, on which the two major effects of alloyed elements are indicated lowering of the dissolution current in the active region and at the active-passive transition, and broadening of the passive region. A third effect, not illustrated in Fig. 3-16 but which will be discussed later, is the improvement of the resistance of the alloy to passivity breakdown and localized corrosion. For iron-based alloys, these beneficial effects are obtained with chromium, molybdenum, nickel, and nitrogen. 

The formation of corrosion products, the solubility of corrosion products in the surface electrolyte, and the formation of passive films affect the overall rate of the anodic metal dissolution process and cause deviations from simple rate equations. Passive films distinguish themselves from corrosion products, in the sense that these films tend to be more tightly adherent, are of lower thickness, and provide a higher degree of protection from corrosive attack. Atmospheric corrosive attack on a surface protected by a passive film tends to be of a localized nature. Surface pitting and stress corrosion cracking in aluminum and stainless alloys are examples of such attack. 

The following mechanisms in corrosion behavior have been affected by implantation and have been reviewed (119) (/) expansion of the passive range of potential, (2) enhancement of resistance to localized breakdown of passive film, (J) formation of amorphous surface alloy to eliminate grain boundaries and stabilize an amorphous passive film, (4) shift open circuit (corrosion) potential into passive range of potential, (5) reduce/eliminate attack at second-phase particles, and (6) inhibit cathodic kinetics. 

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