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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 1-11. Illustration of a Typical Concentration Corrosion Cell<br />

1.7.7 Stress Corrosion Cracking. Stress corrosion cracking<br />

(SCC) is the intergranular cracking of a metal caused by<br />

the combined effects of constant tensile stress (internal or<br />

applied) and corrosion. Internal or residual stresses are produced<br />

by cold working, forming, and heat treatment operations<br />

during manufacture of a part and remain concealed in the<br />

part unless stress relief operations are used. Other hidden<br />

stresses are induced in parts when press or shrink fits are used<br />

and when slightly mismatched parts are clamped together with<br />

rivets and bolts. All these stresses add to those caused by<br />

applying normal loads to parts in operation. Metals have<br />

threshold stresses below which stress corrosion cracking will<br />

not occur. This threshold stress varies from metal to metal and<br />

depends on the characteristics of the stress that is applied. The<br />

following conditions must be present for SCC to occur. The<br />

component or structure must be under a tensile stress. This<br />

tensile stress may be provided by an externally applied service<br />

load or a residual stress resulting from manufacturing procedures<br />

such as rolling, punching, deep drawing, or welding.<br />

The material must also be exposed to an environment that<br />

causes SCC. Whereas all metals will form stress corrosion<br />

cracks in some environment under the proper conditions, there<br />

is no one environment that will cause SCC in all metals. SCC<br />

is most prevalent and of the most concern in high strength<br />

steels, stainless steels (mostly in the austenitic group), high<br />

strength aluminum alloys (2000 and 7000 series), copperbased<br />

alloys, and titanium alloys.<br />

1.7.8 Hydrogen Embrittlement. Hydrogen embrittlement is<br />

the weakening of materials such as high-strength steel (typically<br />

180 Ksi and above), some high-strength aluminum, titanium,<br />

and some types of stainless steels when they are<br />

exposed to acidic materials such as acid paint removers, acidic<br />

metal pretreatments and cleaners, plating solutions, and some<br />

alkaline materials. This occurs when the materials causes a<br />

cathodic reaction on the metal surface that produces hydrogen.<br />

The hydrogen diffuses into the bulk metal, accumulating at<br />

grain boundaries and weldments weakening the structure. If<br />

the part is under load or contains residual manufacturing<br />

stresses, sudden catastrophic failure occurs when the part can<br />

no longer sustain the internal and/or applied stresses. Hydrogen<br />

embrittlement has been known to occur in parts stressed to<br />

only 15% of nominal tensile strength.<br />

1.7.9 Corrosion Fatigue. Corrosion fatigue is the cracking<br />

of metals caused by the combined effects of cyclic stress and<br />

corrosion and is very similar to stress corrosion cracking. If it<br />

is in a corrosive environment, no metal is immune to some<br />

reduction in resistance to cyclic stressing. Corrosion fatigue<br />

failure occurs in two stages. During the first stage, the combined<br />

action of corrosion and cyclic stress damages the metal<br />

by pitting and forming cracks in the pitted area. The second<br />

stage is the continuation of crack propagation, in which the<br />

rate of cracking is controlled by. In simplified terms, corrosion<br />

fatigue is mechanical fatigue aggravated by a corrosive environment.<br />

In corrosion fatigue, the corrosive environment<br />

causes a lowering or reduction of the fatigue limit (the ability<br />

of a metal to resist fatigue cracking) of a metal as it undergoes<br />

cycles of stress. In the absence of a corrosive environment,<br />

this same metal would be able to withstand significantly more<br />

cycles of stress before cracking. Corrosion fatigue seems to be<br />

most prevalent in environments that cause pitting corrosion.<br />

1.7.10 Filiform Corrosion. Filiform corrosion is a special<br />

form of oxygen concentration cell corrosion (or crevice corrosion)<br />

that occurs on metal surfaces having an organic coating<br />

system. It is recognizable by its characteristic wormlike trace<br />

of corrosion products beneath the paint film (see Figure 1-12).<br />

Filiform occurs when the relative humidity of the air is<br />

between 78% and 90% and when the surface is slightly acidic.<br />

It starts at breaks in the coating system (such as scratches and<br />

cracks around fasteners and seams) and proceeds underneath<br />

the coating because of the diffusion of water vapor and oxygen<br />

from the air through the coating. Filiform corrosion can attack<br />

steel, magnesium, and aluminum surfaces and may lead to<br />

more serious corrosion in some locations. Filiform corrosion<br />

can be prevented by: storing equipment in an environment<br />

with a relative humidity below 70%; using coating systems<br />

with a low rate of diffusion for oxygen and water vapors;<br />

maintaining coatings in good conditions; and washing equipment<br />

to remove acidic contaminants from the surface (such as<br />

those created by air pollutants). Filiform corrosion most often<br />

occurs in humid environments. Once the humidity drops<br />

below 65%, Filiform corrosion stops. When the humidity rises<br />

above 95%, blisters form rather than filaments. Filiform corrosion<br />

forms mostly on steel, aluminum, magnesium, and zinc.<br />

1-11

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