Corrosion Chemistry

BASIC CONCEPT OF CORROSION

Corrosion is the gradual destruction of materials, (usually metals), by chemical reaction with its environment.Corrosion is the deterioration of materials by chemical interaction with their environment.The term corrosion is sometimes also applied to the degradation of plastics, concrete and wood, but generally refers to metals. The most widely used metal is iron (usually as steel) and the following discussion is mainly related to its corrosion.

In the most common use of the word, it means electrochemical oxidation of metals in reaction with an oxidant such as oxygen. Rusting, the formation of iron oxides, is a well-known example of electrochemical corrosion. This type of damage typically produces oxide(s) or salt(s) of the original metal. Corrosion can also occur in materials other than metals, such as ceramics or polymers, although in this context, the term degradation is more common. Corrosion degrades the useful properties of materials and structures including strength, appearance and permeability to liquids and gases.

Many structural alloys corrode merely from exposure to moisture in air, but the process can be strongly affected by exposure to certain substances. Corrosion can be concentrated locally to form a pit or crack, or it can extend across a wide area more or less uniformly corroding the surface. Because corrosion is a diffusion-controlled process, it occurs on exposed surfaces. As a result, methods to reduce the activity of the exposed surface, such as passivation and chromate conversion, can increase a material's corrosion resistance. However, some corrosion mechanisms are less visible and less predictable. Rust is the most familiar example of corrosion.

Metals corrode because we use them in environments where they are chemically unstable. Only copper and the precious metals (gold, silver, platinum, etc.) are found in nature in their metallic state. All other metals, to include iron-the metal most commonly used-are processed from minerals or ores into metals which are inherently unstable in their environments.

There are many elements that affect the type, speed, cause and seriousness of metal corrosion. Corrosion contributes to the failure of any metal that it starts to consume. Therefore, proper and enough protection of metals from corrosion help the equipment and structures to last longer and look better. As prevention is always better than cure, it is the owner’s responsibility to observe and take the necessary actions to maintain the appearance and quality of your belongings – be it appliances, automobiles, outdoor equipment, etc… But if you are not certain what method to use, it is best to consult an expert. Remember, incorrect methods in treating metal corrosion can damage your things and might even cost you more.

Metal Corrosion happens when metals are exposed to moisture in the air. This is because most metals react with oxygen which creates rust and eventually leads to corrosion. The end result of corrosion on various appliances, vehicles and other items that include metal components.

Technically, metal corrosion is the process that happens when properties within a particular material start to deteriorate, after exposure to the elements that occur within the environment. Metal Corrosion can be concentrated locally to form a pit or crack, or it can even extend across a large area more or less corroding the surface. Usually metal corrosion occurs on areas exposed to the elements. Metals corrode because they are used in environments where they are chemically unstable. Only copper and precious metals such as gold, silver and platinum are found in nature in their metallic state. All other metals, including the most commonly used which is iron, are processed from minerals or ores into metals and are inherently unstable in their environments.

Metal corrosion can cause extensive problems, but thankfully, there are ways to prevent this by increasing the durability and wear of a product with metal parts. Below are 10 ways on how you can aim to prevent corrosion.

Tips on how to Prevent Metal Corrosion:

Choose products that are made of non-corrosive metals like stainless steel and aluminum.

Metal Corrosion can be best controlled by maintaining a dry environment using suitable moisture barriers and drying agents.

Make sure that your electrical connections are clean.

To prevent metal corrosion on a car or truck, apply a thin coating of petroleum jelly after you clean the terminal.

Always clean and dry the blades of garden tools after every use as this eliminates moisture. Also wash away soil from shovels, hoes and rakes before storing them in a cool and dry place. In addition, wash your garden tools with soap and water, dry them and rub motor oil on the metal parts before you put them away for winter season.

Coat metals with oil, paint, grease or varnish because it can prevent corrosion.

Utilize cleaning agents like soaps, solvents, emulsion compounds and chemicals to efficiently get rid of oil, grease, dirt and other unwanted foreign deposits and follow the correct procedures in applying them.

Metal Corrosion that has already formed on car batteries can be removed by using a mix of cola and baking soda to create a paste. The paste will eat at the corrosion.

To prevent soil corrosion, install correctly copper or copper alloy plumbing underground. The main reasons that lead to corrosion of copper pipelines are poor drainage and moisture. A loose layer of backfill such as limestone or pea level must be put down in the trench before laying copper pipes.

Galvanizing also provides metal corrosion protection. This is the process of giving a thin coating of zinc or steel material by immersing the object in a bath primarily composed of molten zinc. Galvanizing is an efficient way to protect steel because even if the surface is scratched, the zinc still protects the underlying layer. This process is widely used by the automotive industry.

Galvanic corrosion

 Galvanic corrosion occurs when two different metals have physical or electrical contact with each other and are immersed in a common electrolyte, or when the same metal is exposed to electrolyte with different concentrations. In a galvanic couple, the more active metal (the anode) corrodes at an accelerated rate and the more noble metal (the cathode) corrodes at a retarded rate. When immersed separately, each metal corrodes at its own rate. What type of metal(s) to use is readily determined by following the galvanic series. For example, zinc is often used as a sacrificial anode for steel structures. Galvanic corrosion is of major interest to the marine industry and also anywhere water (containing salts) contacts pipes or metal structures.

 Factors such as relative size of anode, types of metal, and operating conditions (temperature, humidity, salinity, etc.) affect galvanic corrosion. The surface area ratio of the anode and cathode directly affects the corrosion rates of the materials. Galvanic corrosion is often utilized in sacrificial anodes.

Corrosion removal

Often it is possible to chemically remove the products of corrosion. For example [phosphoric acid] in the form of [naval jelly] is often applied to ferrous tools or surfaces to remove rust. Corrosion removal should not be confused with electropolishing, which removes some layers of the underlying metal to make a smooth surface. For example, phosphoric acid may also be used to electropolish copper but it does this by removing copper, not the products of copper corrosion.

There are various ways of protecting metals from corrosion including painting, hot dip galvanizing, and combinations of these.

Intrinsic chemistry

Gold nuggets do not naturally corrode, even on a geological time scale.

The materials most resistant to corrosion are those for which corrosion is thermodynamically unfavorable. Any corrosion products of gold or platinum tend to decompose spontaneously into pure metal, which is why these elements can be found in metallic form on Earth and have long been valued. More common "base" metals can only be protected by more temporary means.

Some metals have naturally slow reaction kinetics, even though their corrosion is thermodynamically favorable. These include such metals as zinc, magnesium, and cadmium. While corrosion of these metals is continuous and ongoing, it happens at an acceptably slow rate. An extreme example is graphite, which releases large amounts of energy upon oxidation, but has such slow kinetics that it is effectively immune to electrochemical corrosion under normal conditions.

Passivation

Passivation refers to the spontaneous formation of an ultrathin film of corrosion products known as passive film, on the metal's surface that act as a barrier to further oxidation. The chemical composition and microstructure of a passive film are different from the underlying metal. Typical passive film thickness on aluminium, stainless steels and alloys is within 10 nanometers. The passive film is different from oxide layers that are formed upon heating and are in the micrometer thickness range – the passive film recovers if removed or damaged whereas the oxide layer does not. Passivation in natural environments such as air, water and soil at moderate pH is seen in such materials as aluminium, stainless steel, titanium, and silicon. Passivation is primarily determined by metallurgical and environmental factors. Some conditions that inhibit passivation include high pH for aluminium and zinc, low pH or the presence of chloride ions for stainless steel, high temperature for titanium (in which case the oxide dissolves into the metal, rather than the electrolyte) and fluoride ions for silicon. On the other hand, unusual conditions may result in passivation of materials that are normally unprotected, as the alkaline environment of concrete does for steel rebar. Exposure to a liquid metal such as mercury or hot solder can often circumvent passivation mechanisms. Passivation is primarily determined by metallurgical and environmental factors.

Corrosion in passivated materials

Passivation is extremely useful in mitigating corrosion damage, however even a high-quality alloy will corrode if its ability to form a passivating film is hindered. Proper selection of the right grade of material for the specific environment is important for the long-lasting performance of this group of materials. If breakdown occurs in the passive film due to chemical or mechanical factors, the resulting major modes of corrosion may include pitting corrosion, crevice corrosion and stress corrosion cracking.

Pitting corrosion

The scheme of pitting corrosion

Certain conditions, such as low concentrations of oxygen or high concentrations of species such as chloride which complete as anions, can interfere with a given alloy's ability to re-form a passivating film. In the worst case, almost all of the surface will remain protected, but tiny local fluctuations will degrade the oxide film in a few critical points. Corrosion at these points will be greatly amplified, and can cause corrosion pits of several types, depending upon conditions. While the corrosion pits only nucleate under fairly extreme circumstances, they can continue to grow even when conditions return to normal, since the interior of a pit is naturally deprived of oxygen and locally the pH decreases to very low values and the corrosion rate increases due to an autocatalytic process. In extreme cases, the sharp tips of extremely long and narrow corrosion pits can cause stress concentration to the point that otherwise tough alloys can shatter; a thin film pierced by an invisibly small hole can hide a thumb sized pit from view. These problems are especially dangerous because they are difficult to detect before a part or structure fails. Pitting remains among the most common and damaging forms of corrosion in passivated alloys but it can be prevented by control of the alloy's environment.

Crevice corrosion

Crevice corrosion is a localized form of corrosion occurring in confined spaces (crevices), to which the access of the working fluid from the environment is limited. Formation of a differential aeration cell leads to corrosion inside the crevices. Examples of crevices are gaps and contact areas between parts, under gaskets or seals, inside cracks and seams, spaces filled with deposits and under sludge piles. Crevice corrosion is influenced by the crevice type (metal-metal, metal-nonmetal), crevice geometry (size, surface finish), and metallurgical and environmental factors. A critical crevice corrosion temperature is commonly used to rank a material's resistance to crevice corrosion.

Microbial corrosion

Microbial corrosion, or commonly known as microbiologically influenced corrosion (MIC), is a corrosion caused or promoted by microorganisms, usually chemoautotrophs. It can apply to both metallic and non-metallic materials, in the presence or absence of oxygen. Sulfate-reducing bacteria are active in the absence of oxygen (anaerobic); they produce hydrogen sulfide, causing sulfide stress cracking. In the presence of oxygen (aerobic), some bacteria may directly oxidize iron to iron oxides and hydroxides, other bacteria oxidize sulfur and produce sulfuric acid causing biogenic sulfide corrosion. Concentration cells can form in the deposits of corrosion products, leading to localized corrosion.

Accelerated low-water corrosion

Accelerated low-water corrosion (ALWC) is a particularly aggressive form of MIC that affects steel piles in seawater near the low water tide mark. It is characterized by an orange sludge, which smells of hydrogen sulfide when treated with acid. Corrosion rates can be very high and design corrosion allowances can soon be exceeded leading to premature failure of the steel pile.[5] Piles that have been coating and have cathodic protection installed at the time of construction are not susceptible to ALWC. For unprotected piles, sacrificial anodes can be installed local to the affected areas to inhibit the corrosion or a complete retrofitted sacrificial anode system can be installed. Affected areas can also be treated electrochemically by using an electrode to first produce chlorine to kill the bacteria, and then to produced a calcareous deposit, which will help shield the metal from further attack.

Temperature corrosion

High-temperature corrosion is chemical deterioration of a material (typically a metal) as a result of heating. This non-galvanic form of corrosion can occur when a metal is subjected to a hot atmosphere containing oxygen, sulfur or other compounds capable of oxidizing (or assisting the oxidation of) the material concerned. For example, materials used in aerospace, power generation and even in car engines have to resist sustained periods at high temperature in which they may be exposed to an atmosphere containing potentially highly corrosive products of combustion. The products of high-temperature corrosion can potentially be turned to the advantage of the engineer. The formation of oxides on stainless steels, for example, can provide a protective layer preventing further atmospheric attack, allowing for a material to be used for sustained periods at both room and high temperatures in hostile conditions. Such high-temperature corrosion products, in the form of compacted oxide layer glazes, prevent or reduce wear during high-temperature sliding contact of metallic (or metallic and ceramic) surfaces.

Metal Dusting

Metal dusting is a catastrophic form of corrosion that occurs when susceptible materials are exposed to environments with high carbon activities, such as synthesis gas and other high-CO environments. The corrosion manifests itself as a break-up of bulk metal to metal powder. The suspected mechanism is firstly the deposition of a graphite layer on the surface of the metal, usually from carbon monoxide (CO) in the vapour phase. This graphite layer is then thought to form metastable M3C species (where M is the metal), which migrate away from the metal surface. However, in some regimes no M3C species is observed indicating a direct transfer of metal atoms into the graphite layer.

Galvanization

Galvanized surface

Plating, painting, and the application of enamel are the most common anti-corrosion treatments. They work by providing a barrier of corrosion-resistant material between the damaging environment and the structural material. Aside from cosmetic and manufacturing issues, there are tradeoffs in mechanical flexibility versus resistance to abrasion and high temperature. Platings usually fail only in small sections, and if the plating is more noble than the substrate (for example, chromium on steel), a galvanic couple will cause any exposed area to corrode much more rapidly than an unplated surface would. For this reason, it is often wise to plate with active metal such as zinc or cadmium. Painting either by roller or brush is more desirable for tight spaces; spray would be better for larger coating areas such as steel decks and waterfront applications. Flexible polyurethane coatings, like Durabak-M26 for example, can provide an anti-corrosive seal with a highly durable slip resistant membrane. Painted coatings are relatively easy to apply and have fast drying times although temperature and humidity may cause dry times to vary.

Reactive coatings

If the environment is controlled (especially in recirculating systems), corrosion inhibitors can often be added to it. These form an electrically insulating or chemically impermeable coating on exposed metal surfaces, to suppress electrochemical reactions. Such methods obviously make the system less sensitive to scratches or defects in the coating, since extra inhibitors can be made available wherever metal becomes exposed. Chemicals that inhibit corrosion include some of the salts in hard water (Roman water systems are famous for their mineral deposits), chromates, phosphates, polyaniline, other conducting polymers and a wide range of specially-designed chemicals that resemble surfactants (i.e. long-chain organic molecules with ionic end groups).

Anodization

Aluminium alloys often undergo a surface treatment. Electrochemical conditions in the bath are carefully adjusted so that uniform pores several nanometers wide appear in the metal's oxide film. These pores allow the oxide to grow much thicker than passivating conditions would allow. At the end of the treatment, the pores are allowed to seal, forming a harder-than-usual surface layer. If this coating is scratched, normal passivation processes take over to protect the damaged area. Anodizing is very resilient to weathering and corrosion, so it is commonly used for building facades and other areas that the surface will come into regular contact with the elements. Whilst being resilient, it must be cleaned frequently. If left without cleaning, panel edge staining will naturally occur.

Biofilm coatings

A new form of protection has been developed by applying certain species of bacterial films to the surface of metals in highly corrosive environments. This process increases the corrosion resistance substantially. Alternatively, antimicrobial-producing biofilms can be used to inhibit mild steel corrosion from sulfate-reducing bacteria.

Controlled permeability formwork

Controlled permeability formwork (CPF) is a method of preventing the corrosion of reinforcement by naturally enhancing the durability of the cover during concrete placement. CPF has been used in environments to combat the effects of carbonation, chlorides, frost and abrasion.

Cathodic protection

Cathodic protection (CP) is a technique to control the corrosion of a metal surface by making that surface the cathode of an electrochemical cell. Cathodic protection systems are most commonly used to protect steel, water, and fuel pipelines and tanks; steel pier piles, ships, and offshore oil platforms.

Sacrificial anode protection

Sacrificial anode in the hull of a ship

For effective CP, the potential of the steel surface is polarized (pushed) more negative until the metal surface has a uniform potential. With a uniform potential, the driving force for the corrosion reaction is halted. For galvanic CP systems, the anode material corrodes under the influence of the steel, and eventually it must be replaced. The polarization is caused by the current flow from the anode to the cathode, driven by the difference in electrochemical potential between the anode and the cathode.

Impressed current cathodic protection

For larger structures, galvanic anodes cannot economically deliver enough current to provide complete protection. Impressed current cathodic protection (ICCP) systems use anodes connected to a DC power source (such as a cathodic protection rectifier). Anodes for ICCP systems are tubular and solid rod shapes of various specialized materials. These include high silicon cast iron, graphite, mixed metal oxide or platinum coated titanium or niobium coated rod and wires.

Anodic protection

Anodic protection impresses anodic current on the structure to be protected (opposite to the cathodic protection). It is appropriate for metals that exhibit passivity (e.g., stainless steel) and suitably small passive current over a wide range of potentials. It is used in aggressive environments, e.g., solutions of sulfuric acid.

Rate of corrosion

A simple test for measuring corrosion is the weight loss method.[citation needed] The method involves exposing a clean weighed piece of the metal or alloy to the corrosive environment for a specified time followed by cleaning to remove corrosion products and weighing the piece to determine the loss of weight. The rate of corrosion (R) is calculated as

R = KW/(ρAt)

where k is a constant, W is the weight loss of the metal in time t, A is the surface area of the metal exposed, and ρ is the density of the metal (in g/cm³).

Economic impact

Rust is one of the most common causes of bridge accidents. As rust has a much higher volume than the originating mass of iron, its build-up can also cause failure by forcing apart adjacent parts

Similarly, corrosion of concrete-covered steel and iron can cause the concrete to spall, creating severe structural problems. It is one of the most common failure modes of reinforced concrete bridges. Measuring instruments based on the half-cell potential can detect the potential corrosion spots before total failure of the concrete structure is reached.

Until 20–30 years ago; galvanized steel pipe was used extensively in the potable water systems for single and multi-family residents as well as commercial and public construction. Today, these systems have long consumed the protective zinc and are corroding internally resulting in poor water quality and pipe failures.[8] The economic impact on homeowners, condo dwellers, and the public infrastructure is estimated at 22 billion dollars as insurance industry braces for a wave of claims due to pipe failures.

CORROSION IN NON-METALS

Most ceramic materials are almost entirely immune to corrosion. The strong chemical bonds that hold them together leave very little free chemical energy in the structure; they can be thought of as already corroded. When corrosion does occur, it is almost always a simple dissolution of the material or chemical reaction, rather than an electrochemical process. A common example of corrosion protection in ceramics is the lime added to soda-lime glass to reduce its solubility in water; though it is not nearly as soluble as pure sodium silicate, normal glass does form sub-microscopic flaws when exposed to moisture. Due to its brittleness, such flaws cause a dramatic reduction in the strength of a glass object during its first few hours at room temperature.

Corrosion of polymers

Ozone cracking in natural rubber tubing

Polymer degradation involves several complex and often poorly-understood physiochemical processes. These are strikingly different from the other processes discussed here, and so the term "corrosion" is only applied to them in a loose sense of the word. Because of their large molecular weight, very little entropy can be gained by mixing a given mass of polymer with another substance, making them generally quite difficult to dissolve. While dissolution is a problem in some polymer applications, it is relatively simple to design against. A more common and related problem is swelling, where small molecules infiltrate the structure, reducing strength and stiffness and causing a volume change. Conversely, many polymers (notably flexible vinyl) are intentionally swelled with plasticizers, which can be leached out of the structure, causing brittleness or other undesirable changes. The most common form of degradation, however, is a decrease in polymer chain length. Mechanisms which break polymer chains are familiar to biologists because of their effect on DNA: ionizing radiation (most commonly ultraviolet light), free radicals, and oxidizers such as oxygen, ozone, and chlorine. Ozone cracking is a well-known problem affecting natural rubber for example. Additives can slow these process very effectively, and can be as simple as a UV-absorbing pigment (i.e., titanium dioxide or carbon black). Plastic shopping bags often do not include these additives so that they break down more easily as litter.

Corrosion of glasses

Glass corrosion

Glass disease is the corrosion of silicate glasses in aqueous solutions. It is governed by two mechanisms: diffusion-controlled leaching (ion exchange) and hydrolytic dissolution of the glass network.  Both mechanisms strongly depend on the pH of contacting solution.