This chapter discusses some important factors involved in the atmospheric corrosion of engineering materials. The discussion begins with a description of elements necessary for the operation of a galvanic corrosion cell and corrosion reactions, followed by the types of atmospheric corrosion attack. Some of the atmospheric parameters and their effects on the corrosion of several metals are then reviewed. The following sections provide information on air chemistry, principal pollutants inducing corrosion, thermodynamics as well as models for prediction of atmospheric corrosion, and use of Pourbaix diagrams. The phenomenon of precipitation runoff on the corroded metal surface is then discussed. The chapter also describes the role of microbes or bacteria in the corrosion of metals. It concludes by providing information on the trends in atmospheric corrosion research and methods.

Corrosion can be defined as a chemical or electrochemical reaction between a material and its environment that causes the material and its properties to degrade. In most cases, it refers to the electrochemical oxidation of metals accompanied by the production of oxides or salts of the base material. This chapter discusses the process of corrosion and how to prevent or mitigate its effects. It describes several forms of corrosion, including uniform, intergranular, pitting, crevice, and stray-current corrosion, and the effects of stress-corrosion cracking, corrosion fatigue, and selective leaching. It discusses the use of corrosion inhibitors, cathodic and anodic protection, pH control, and Pourbaix diagrams.

Corrosion is a key subject for more or less all classes of alloys that fall within the broad definition of stainless steels because these alloys were developed with the intention of preventing corrosion. This chapter provides an introduction to the fundamentals of electrochemical theory as it pertains to corrosion resistance of stainless steels. The discussion provides an overview of electrochemical reactions, Faraday's law, the Nernst equation, galvanic versus electrochemical cells, corrosion tendency, and Pourbaix diagrams.

This chapter provides a thorough introduction to the electrochemical thermodynamics that govern electrode reactions associated with corrosion. It begins with a review of the thermodynamic criteria for the stability of chemical reactions based on Gibbs free energy and explains how energies of formation are determined using the oxidation of iron as an example. It then considers how iron reacts with hydrochloric acid, explaining how it can be expressed as two half reactions modeled as electrodes in an electrochemical cell. It goes on to describe the chemical reactions occurring at each electrode, accounting for different variables, mechanisms, and electrochemical effects. The chapter concludes with an in-depth review of Pourbaix diagrams, explaining what they reveal about the stability of metal-water systems and the formation of corrosion products.

This chapter discusses the complex polarization characteristics of active-passive metals and addresses related problems in interpreting their corrosion behavior. It begins by presenting several experimentally derived polarization curves for iron, comparing and contrasting them with the iron-water Pourbaix diagram. It then explains how anodic polarization is extremely sensitive to the environment and, as a result, a reasonably complete curve for a given metal-environment system usually can only be inferred. It goes on to describe how such curves are constructed, demonstrating the procedures for a wide range of alloys and environments. The examples also show how factors such as alloy concentration, crystal lattice orientation, temperature, and dissolved oxygen affect corrosion behavior.