Hot dip galvanizing protects steel from corrosion by providing a thick, tough, metallurgically bonded zinc envelope, which completely covers the steel surface and seals it from the corrosive action of its environment.
The hot dip galvanized coating provides outstanding abrasion resistance. Where there is damage or minor discontinuity in the sealing coat of zinc, protection of the steel is maintained by the cathodic action of the surrounding galvanized coating.
The durability of hot dip galvanized steel is particularly important in Australia and New Zealand where 85% of the population live within 50 kilometres of the coast. Corrosion rates for structural steel in these coastal regions vary from 1µm to 1mm per year, while the hot dip galvanized coating can protect structural steel by providing barrier and cathodic protection for over 50 years close to calm seas and over 30 years when the steel is at least 200m from surf beaches. Inland, examples of the original hot dip galvanized overland telegraph poles installed in the 1870’s to counter the termites can still be found with their original coating intact and protecting the steel.
The galvanized coating
The galvanizing process produces a durable, abrasion-resistant coating of metallic zinc and zinc-iron alloy layers bonded metallurgically to the steel base and completely covering the work piece.
No other coating for steel matches galvanizing’s unique combination of properties and advantages:
- For most classes of steelwork, galvanizing provides the lowest long-term cost. In many cases galvanizing also provides lowest initial cost.
- The galvanized coating becomes part of the steel surface it protects.
- The unique metallurgical structure of the galvanized coating provides outstanding toughness and resistance to mechanical damage in transport, erection, and service.
- The galvanized coating is subject to corrosion at a predictably slow rate, between one-seventeenth and one-eightieth that of steel, depending on the environment to which it is exposed.
- Galvanizing’s cathodic protection for steel ensures that small areas of the base steel exposed through severe impacts or abrasion, are protected from corrosion by the surrounding galvanized coating.
- An inherent advantage of the process is that a standard minimum coating thickness is applied.
- During galvanizing the work is completely immersed in molten zinc and the entire surface is coated, even recesses and returns which often cannot be coated using other processes. If required, internal surfaces of vessels and containers can be coated simultaneously.
- Galvanized coatings are virtually ‘self-inspecting’ because the reaction between steel and molten zinc in the galvanizing bath does not occur unless the steel surface is chemically clean. Therefore, a galvanized coating which appears sound and continuous is sound and continuous.
- Galvanizing is a highly versatile process. Items ranging from small fasteners and threaded components, up to massive structural members can be coated.
- The mechanical properties of commonly galvanized steels are not significantly affected by galvanizing.
- Galvanizing provides outstanding corrosion performance in a wide range of environments.
- ‘Duplex’ coatings of galvanizing-plus-paint are often the most economical solution to the problem of protecting steel in highly corrosive environments. Such systems provide a synergistic effect in which the life of the combined coatings exceeds the total life of the two coatings if they were used alone.
The nature of corrosion
The corrosion of a metal is a physiochemical interaction between a metal and its environment which results in changes in the properties of the metal. Corrosion of metal results in the degradation of the metal to an oxidized form, for example the conversion of metallic iron to rust. For corrosion to occur it is necessary that the metal is in contact with an electrolyte, typically surface moisture including condensation or rain and ponding water. The electrolyte facilitates the flow of charge and matter and enables the electrochemical reaction to proceed. It is a key requirement for metal corrosion. These electrolytes serve to allow formation of small electrolytic cells on the metal surface, which then results in corrosion.
Another factor influencing the corrosion of a metal is the difference in electric potential on the surface of the metal, which can be caused by variations in composition, the presence of impurities, uneven internal stresses, or a non-uniform environment.
Each electrolytic cell comprises a positive electron-producing anode and a negative cathode. Negatively charged electrons flow from anode to cathode. The loss of electrons converts some atoms of the anode to positively charged ions which in turn react with negatively charged ions in the electrolyte. This reaction between anode and electrolyte causes disintegration and corrosion of the anode metal. There is no corrosion of the cathode metal.
The corrosion of steel is described in more detail in the following graphics.
Corrosion of steel
Differences in electrical potential on the steel surface are caused by non-uniformity of the surface composition, by surface moisture or by the electrolyte in which it is immersed. Small electrolytic cells are formed comprising anodes and cathodes.
As the result of differences in electrical potential within the cell, negatively charged electrons flow from the anode to the cathode and iron atoms in the anode area are converted to positively charged ions.
The positive iron ions from the anode attract and react with negatively charged hydroxyl ions in the electrolyte to form iron oxide (i.e., rust). Negatively charged electrons react at the cathode surface with positively charged hydrogen ions in the electrolyte to form hydrogen gas.
Under suitable conditions corrosion occurs at the rate of billions of complete reactions every second and soon results in a layer of rust appearing over the surface of the anodic area.
The anodic and cathodic areas on a piece of steel are microscopic in size. When greatly magnified, the surface might appear as the mosaic of anodes and cathodes visualised here, all electrically connected by the underlying steel. Corrosion occurs in the anodic areas.
As anodic areas corrode new material of different composition and structure is exposed. This results in changes in electrical potentials, causing anodes and cathodes to exchange roles, though not all at once, and areas previously not corroded are now attacked. These processes may continue until the steel is entirely consumed.
Hot dip galvanizing – Protecting steel 3 ways.
1. Barrier protection
Barrier protection, as its name implies, works by providing an impermeable barrier between the steel item and its environment. Galvanizing provides barrier protection in two ways: firstly, the galvanized layer provides a protective physical envelope around the steel; secondly, the galvanized layer also develops a protective patina on its surface upon exposure to the environment which serves to further extend the life of the galvanized coatings.
The barrier protection qualities of galvanized steel are also enhanced by the fact that it is immune to ultraviolet radiation and thus will not degrade on exposure to Australia’s harsh environment. Most other corrosion protection coatings will degrade on exposure to solar radiation. This is usually one of the key limiting factors to the performance of such coatings.
The problem with conventional barrier protection, such as painting, is that it will not prevent corrosion if the base steel is exposed due to mechanical impact damage or abrasion of the coating. In fact, some barrier protection paints allow corrosion to proceed undetected in the form of under-film corrosion. In the event of severe mechanical damage and exposure of the base steel to the environment, galvanizing also provides cathodic protection. The galvanizing performs in a similar way to other sacrificial protection systems, except in this case the sacrificial anode is distributed over the article to be protected and electrical continuity is assured. The cathodic protection characteristics of galvanizing ensure that mechanical damage does not result in concealed under-film corrosion and potential catastrophic failure prevalent in some other protective coatings.
2. Protective Patina
A protective patina is generally made up of insoluble zinc oxides, hydroxides, and carbonates, but can contain other basic zinc salts depending on the environment. Once the patina stabilises, it reduces the exposure of the galvanized coating to the environment, thus considerably slowing the corrosion process. This patina regenerates itself after damage by slowly consuming the zinc in the coating.
The zinc patina begins its development with exposure to oxygen in the atmosphere, forming a layer of zinc oxide on the surface. Moisture from rain or humid air reacts with the zinc oxide to form zinc hydroxide which then reacts with carbon dioxide present in the air to form the tightly adherent, insoluble zinc patina.
3. Cathodic protection
When zinc and steel are in contact in an electrolyte, differences in electrical potential develop and an electrolytic cell is formed. Zinc is more electrochemically active than steel (Figure 1). The zinc therefore becomes the anode for all the steel, preventing the formation of small anodic and cathodic areas on the steel surface.
As a result of the differences in electrical potential within the cell, negatively charged electrons flow from the zinc anode to the steel cathode and zinc atoms in the anode are converted to positively charged zinc ions.
At the cathode surface, negatively charged electrons attract and react with positively charged hydrogen ions from the electrolyte, liberating hydrogen gas. There is no chemical reaction between the steel cathode and the electrolyte. This phenomenon which prevents corrosion of the cathode, is known as cathodic protection. The positively charged zinc ions at the anode surface react with negatively charged hydroxyl ions from the electrolyte and zinc is slowly consumed, providing sacrificial protection for the steel.
Galvanic series of metals in a sea water electrolyte
Figure 2 shows a series of metals arranged left to right in order of electrochemical activity in sea water. Metals on the left of the scale provide cathodic or sacrificial protection to the metals to the right. The scale indicates that magnesium, zinc, and aluminium protect steel. In most normal applications magnesium is highly reactive and is too rapidly consumed. Aluminium forms a resistant oxide coating and its effectiveness in providing cathodic protection is limited.
Cathodic protection of damaged areas
Where continuity of galvanized coating is broken by cut edges, drilled holes or surface damage, small areas of exposed steel are protected from corrosion cathodically by the surrounding coating. Touch up may not be necessary for areas less than 5mm in diameter due to the cathodic protection provided and this sacrificial protection can continue for many years. In service, zinc corrosion product tends to build up in the coating discontinuities, slowing the rate at which the surrounding coating is consumed to protect a damaged area. A practical example of this cathodic protection phenomenon is the uncoated internal threads of certain fasteners. The uncoated internal threads of galvanized nuts are protected from corrosion by the zinc coating on mating bolts and studs.