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TO 35-1-3 - Robins Air Force Base

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<strong>TO</strong> <strong>35</strong>-1-3<br />

Figure 1-7. Example of Pitting Corrosion<br />

Figure 1-6. Example of Galvanic Corrosion - Steel Hinge<br />

Bolted to an Aluminum Door<br />

1.7.3 Pitting Corrosion. The most common corrosion on<br />

aluminum and magnesium alloys is called pitting corrosion<br />

(see Figure 1-7). It is first noticeable as a white or gray powdery<br />

deposit, similar to dust, that blotches the surface. When<br />

the deposits are cleaned away, tiny pits or holes can be seen in<br />

the surface. Pitting corrosion may also occur in other types of<br />

alloys. The combination of small active anodes to large passive<br />

cathodes causes severe pitting. Pitting starts as an<br />

advanced form of uniform etch. It can worsen into very severe<br />

corrosion that results in localized and relatively deep holes in<br />

the metal. Pits are isolated holes that can vary in shape and<br />

size and usually take several months to a year before they<br />

become visible. Pitting is an extremely destructive and insidious<br />

form of corrosion. It causes equipment to fail because of<br />

perforation with very little weight or material loss on the<br />

entire structure. It is also difficult to detect because the pits are<br />

often covered with corrosion products. Pitting usually initiates<br />

at anodic points on a metal surface such as breaks in protective<br />

coatings or films, scratches, and irregularities that are exposed<br />

to an aggressive electrolyte. Even though a pit is slow to initiate,<br />

once started, it will progress at an ever-increasing rate<br />

and will tend to undercut the surface as it grows.<br />

1.7.4 Intergranular Corrosion. Intergranular corrosion (see<br />

Figure 1-8) is an attack on the grain boundaries of the metal. A<br />

highly magnified cross-section of any commercial alloy shows<br />

the granular structure of the metal. This consists of quantities<br />

of individual grains, each having a clearly defined boundary<br />

that chemically differ from the metal within the grain. The<br />

grain boundaries are frequently anodic (i.e., tend to corrode<br />

more easily) to the metal within the grain. When in contact<br />

with an electrolyte, rapid corrosion occurs at the grain boundaries.<br />

1.7.5 Exfoliation Corrosion. Exfoliation corrosion (see Figure<br />

1-9) is an advanced form of intergranular corrosion and<br />

occurs when the surface grains of a metal are lifted up by the<br />

force of expanding corrosion products occurring at the metal<br />

grain boundaries. The lifting up or swelling is visible evidence<br />

of exfoliation corrosion. Exfoliation occurs on extruded,<br />

rolled, wrought, and forged high strength aluminum and magnesium<br />

parts.<br />

1.7.6 Concentration/Crevice Corrosion. Crevice corrosion<br />

(see Figure 1-10 and Figure 1-11) occurs when the electrolyte<br />

in a crevice has a different concentration than the area<br />

adjacent to the crevice. This type of corrosion is also known as<br />

concentration cell corrosion. Electrolyte inside the crevice<br />

contains less oxygen and more metal ions than electrolyte just<br />

outside the crevice. As a result, the metal surfaces have different<br />

activities, even though they may be part of the same metal,<br />

and corrosion occurs inside the crevice. This form of corrosion<br />

often occurs between faying surfaces or when a surface is<br />

covered by a foreign material (such as dirt) or under gaskets,<br />

rubber, or plastic tape. The mechanisms involved in crevice<br />

corrosion are very similar to pitting corrosion. Crevice corrosion<br />

most often occurs where there are stagnant solutions<br />

(electrolytes) in holes, gasket surfaces, lap joints, under surface<br />

deposits (sand, dirt, corrosion products, etc.), and in crevices<br />

under bolt and rivet heads. To become a site for corrosion,<br />

a crevice must be wide enough to allow liquid entry but narrow<br />

enough to keep the liquid stagnant. As with pitting, crevice<br />

corrosion is slow to start, but once started, progresses at<br />

ever increasing rates (due to various electrochemical factors).<br />

Crevice corrosion is also most intense in solutions containing<br />

chlorides (saltwater). Metals susceptible to pitting (stainless<br />

steel, aluminum, magnesium) are also susceptible to crevice<br />

corrosion. However, not all metals that are susceptible to crevice<br />

corrosion will be susceptible to pitting. Three general types<br />

of crevice corrosion are: Metal ion concentration cells, Oxygen<br />

concentration cells, Active-passive cells.<br />

1-9

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