Corrosion Theory
Humans have most likely been trying to understand and control corrosion for as long as they have been using metal objects. The most important periods of prerecorded history are named for the metals that were used for tools and weapons (Iron Age, Bronze Age). With a few exceptions, metals are unstable in ordinary aqueous environments. Metals are usually extracted from ores through the application of a considerable amount of energy.
Certain environments offer opportunities for these metals to combine chemically with elements to form compounds and return to their lower energy levels. A modern and comprehensive document on the subject is the second edition of the classic CORROSION BASICS textbook. Some excerpts of that document are used here.
Corrosion is the primary means by which metals deteriorate. Most metals corrode on contact with water (and moisture in the air), acids, bases, salts, oils, aggressive metal polishes, and other solid and liquid chemicals. Metals will also corrode when exposed to gaseous materials like acid vapors, formaldehyde gas, ammonia gas, and sulfur containing gases. Corrosion specifically refers to any process involving the deterioration or degradation of metal components. The best known case is that of the rusting of steel. Corrosion processes are usually electrochemical in nature, having the essential features of a battery.
When metal atoms are exposed to an environment containing water molecules they can give up electrons, becoming themselves positively charged ions, provided an electrical circuit can be completed. This effect can be concentrated locally to form a pit or, sometimes a crack, or it can extend across a wide area to produce general wastage. Localized corrosion that leads to pitting may provide sites for fatigue initiation and, additionally, corrosive agents like seawater may lead to greatly enhanced growth of the fatigue crack. Pitting corrosion also occurs much faster in areas where microstructural changes have occurred due to welding operations.
The corrosion process (anodic reaction) of the metal dissolving as ions generates some electrons, as shown in the simple model on the left, that are consumed by a secondary process (cathodic reaction). These two processes have to balance their charges. The sites hosting these two processes can be located close to each other on the metal's surface, or far apart depending on the circumstances. This simple observation has a major impact in many aspects of corrosion prevention and control, for designing new corrosion monitoring techniques to avoiding the most insidious or localized forms of corrosion.
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