Abstract

This article presents a synthesis of recent studies focused on the corrosion product layers forming on carbon steel in natural seawater and the link between the composition of these layers and the corrosion mechanisms. Additional new experimental results are also presented to enlighten some important points. First, the composition and stratification of the layers produced by uniform corrosion are described. A focus is made on the mechanism of formation of the sulfate green rust because this compound is the first solid phase to precipitate from the dissolved species produced by the corrosion of the steel surface. Secondly, localized corrosion processes are discussed. In any case, they involve galvanic couplings between anodic and cathodic zones of the metal surface and are often associated with heterogeneous corrosion product layers. The variations of the composition of these layers with the anodic/cathodic character of the underlying metal surface, and in particular the changes in magnetite content, are thoroughly described and analyzed to enlighten the self-sustaining ability of the process. Finally, corrosion product layers formed on permanently immersed steel surfaces were exposed to air. Their drying and oxidation induced the formation of akaganeite, a common product of marine atmospheric corrosion that was, however, not detected on the steel surface after the permanent immersion period.

Highlights

  • Seawater is one of the most complex and aggressive media

  • The thorough characterization of the corrosion product layers provided important information that led to a better understanding of the mechanisms of marine corrosion of carbon steel permanently immersed in natural seawater

  • - It is generally admitted that, after a sufficiently long immersion time, anoxic conditions are met at the steel surface and inside the inner part of the corrosion product layer

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Summary

Introduction

Seawater is one of the most complex and aggressive media. Marine corrosion depends on numerous interdependent parameters and combines chemical, biological and mechanical factors. This article reports recent advances in the understanding of localized corrosion processes of carbon steel permanently immersed in natural seawater, obtained through a detailed analysis of the corrosion product layers [26,30,36,41,42,44] These layers, formed on steel surfaces in laboratory experiments or seaport exposure sites, reflect the complexity of iron chemistry in natural seawater. Their composition differs in anodic and cathodic zones [9,41,42] so that they participate actively in the persistence of corrosion cells and favor localized corrosion processes [41]

Materials and Exposure Sites
Characterization of the Corrosion Product Layers
Stratification of the Corrosion Product Layer
Composition of the Corrosion Product Layer
Heterogeneity of the Corrosion Product Layer and Role of Interfacial pH
Variations of the Magnetite Content
Oxidation of the Corrosion Product Layers and FORMATION of Akaganeite
Findings
Conclusions
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