Corrosion Control – Part One (Types)

in Aircraft Cleaning and Corrosion Control

Corrosion Control

Many aircraft structures are made of metal, and the most insidious form of damage to those structures is corrosion. From the moment the metal is manufactured, it must be protected from the deleterious effects of the environment that surrounds it. This protection can be the introduction of certain elements into the base metal, creating a corrosion resistant alloy, or the addition of a surface coating of a chemical conversion coating, metal or paint. While in use, additional moisture barriers, such as viscous lubricants and protectants may be added to the surface.


The introduction of airframes built primarily of composite components has not eliminated the need for careful monitoring of aircraft with regard to corrosion. While the airframe itself may not be subject to corrosion, the use of metal components and accessories within the airframe means the aircraft maintenance technician must be on the alert for the evidence of corrosion when inspecting any aircraft.

This chapter provides an overview to the problems associated with aircraft corrosion. For more in-depth information on the subject, refer to the latest edition of FAA Advisory Circular (AC) 43-4A, Corrosion Control for Aircraft. The advisory circular is an extensive handbook, which deals with the sources of corrosion particular to aircraft structures, as well as steps the aircraft maintenance technician can take in the course of maintaining aircraft that have been attacked by corrosion.

Metal corrosion is the deterioration of the metal by chemical or electrochemical attack. This type of damage can take place internally as well as on the surface. As in the rotting of wood, this deterioration may change the smooth surface, weaken the interior, or damage or loosen adjacent parts.

Water or water vapor containing salt combines with oxygen in the atmosphere to produce the main source of corrosion in aircraft. Aircraft operating in a marine environment, or in areas where the atmosphere contains industrial fumes that are corrosive, are particularly susceptible to corrosive attacks. [Figure 6-1]

Figure 6-1. Seaplane operations.

Figure 6-1. Seaplane operations.

If left unchecked, corrosion can cause eventual structural failure. The appearance of corrosion varies with the metal. On the surface of aluminum alloys and magnesium, it appears as pitting and etching, and is often combined with a gray or white powdery deposit. On copper and copper alloys, the corrosion forms a greenish film; on steel, a reddish corrosion byproduct commonly referred to as rust. When the gray, white, green, or reddish deposits are removed, each of the surfaces may appear etched and pitted, depending upon the length of exposure and severity of attack. If these surface pits are not too deep, they may not significantly alter the strength of the metal; however, the pits may become sites for crack development, particularly if the part is highly stressed. Some types of corrosion burrow between the inside of surface coatings and the metal surface, and can spread until the part fails.

Types of Corrosion

There are two general classifications of corrosion that cover most of the specific forms: direct chemical attack and electrochemical attack. In both types of corrosion, the metal is converted into a metallic compound such as an oxide, hydroxide, or sulfate. The corrosion process always involves two simultaneous changes: The metal that is attacked or oxidized suffers what may be called anodic change, and the corrosive agent is reduced and may be considered as undergoing cathodic change.

Direct Chemical Attack

Direct chemical attack, or pure chemical corrosion, is an attack resulting from a direct exposure of a bare surface to caustic liquid or gaseous agents. Unlike electrochemical attack where the anodic and cathodic changes may be taking place a measurable distance apart, the changes in direct chemical attack are occurring simultaneously at the same point. The most common agents causing direct chemical attack on aircraft are: (1) spilled battery acid or fumes from batteries; (2) residual flux deposits resulting from inadequately cleaned, welded, brazed, or soldered joints; and (3) entrapped caustic cleaning solutions. [Figure 6-2]

Figure 6-2. Direct chemical attack in a battery compartment.

Figure 6-2. Direct chemical attack in a battery compartment.

With the introduction of sealed lead-acid batteries and the use of nickel-cadmium batteries, spilled battery acid is becoming less of a problem. The use of these closed units lessens the hazards of acid spillage and battery fumes.

Many types of fluxes used in brazing, soldering, and welding are corrosive, and they chemically attack the metals or alloys with which they are used. Therefore, it is important to remove residual flux from the metal surface immediately after the joining operation. Flux residues are hygroscopic in nature; that is, they absorb moisture, and unless carefully removed, tend to cause severe pitting.

Caustic cleaning solutions in concentrated form should be kept tightly capped and as far from aircraft as possible. Some cleaning solutions used in corrosion removal are, in themselves, potentially corrosive agents; therefore, particular attention should be directed toward their complete removal after use on aircraft. Where entrapment of the cleaning solution is likely to occur, use a noncorrosive cleaning agent, even though it is less efficient.

Electrochemical Attack

An electrochemical attack may be likened chemically to the electrolytic reaction that takes place in electroplating, anodizing, or in a dry cell battery. The reaction in this corrosive attack requires a medium, usually water, which is capable of conducting a tiny current of electricity. When a metal comes in contact with a corrosive agent and is also connected by a liquid or gaseous path through which electrons may flow, corrosion begins as the metal decays by oxidation. [Figure 6-3] During the attack, the quantity of corrosive agent is reduced and, if not renewed or removed, may completely react with the metal, becoming neutralized. Different areas of the same metal surface have varying levels of electrical potential and, if connected by a conductor, such as salt water, will set up a series of corrosion cells and corrosion will commence.

Figure 6-3. Electrochemical attack.

Figure 6-3. Electrochemical attack.

All metals and alloys are electrically active and have a specific electrical potential in a given chemical environment. This potential is commonly referred to as the metal’s “nobility.” [Figure 6-4] The less noble a metal is, the more easily it can be corroded. The metals chosen for use in aircraft structures are a studied compromise with strength, weight, corrosion resistance, workability, and cost balanced against the structure’s needs.

Figure 6-4. The galvanic series of metals and alloys.

Figure 6-4. The galvanic series of metals and alloys.

The constituents in an alloy also have specific electrical potentials that are generally different from each other. Exposure of the alloy surface to a conductive, corrosive medium causes the more active metal to become anodic and the less active metal to become cathodic, thereby establishing conditions for corrosion. These are called local cells. The greater the difference in electrical potential between the two metals, the greater will be the severity of a corrosive attack, if the proper conditions are allowed to develop.

The conditions for these corrosion reactions are the presence of a conductive fluid and metals having a difference in potential. If, by regular cleaning and surface refinishing, the medium is removed and the minute electrical circuit eliminated, corrosion cannot occur. This is the basis for effective corrosion control. The electrochemical attack is responsible for most forms of corrosion on aircraft structure and component parts.