A cast iron pan.

Iron-cementite meta-stable diagram.

This article needs additional citations for verification. Please help improve this article by adding citations to reliable sources. Unsourced material may be challenged and removed. (October 2008)

Cast iron is iron or a ferrous alloy which has been heated until it liquifies, and is then poured into a mould to solidify. It is usually made from pig iron. The alloy constituents affect its colour when fractured: white cast iron has carbide impurities which allow cracks to pass straight through. Grey cast iron, or grey iron, has graphitic flakes which deflect a passing crack and initiate countless new cracks as the material breaks.

Carbon (C) and silicon (Si) are the main alloying elements, with the amount ranging from 2.1 to 4 wt% and 1 to 3 wt%, respectively. Iron alloys with less carbon content are known as steel. While this technically makes these base alloys ternary Fe-C-Si alloys, the principle of cast iron solidification is understood from the binary iron-carbon phase diagram. Since the compositions of most cast irons are around the eutectic point of the iron-carbon system, the melting temperatures closely correlate, usually ranging from 1,150 to 1,200 °C (2,102 to 2,192 °F), which is about 300 °C (572 °F) lower than the melting point of pure iron.

Cast iron tends to be brittle, except for malleable cast irons. With its relatively low melting point, good fluidity, castability, excellent machinability, resistance to deformation and wear resistance, cast irons have become an engineering material with a wide range of applications and are used in pipes, machines and automotive industry parts, such as cylinder heads (declining usage), cylinder blocks and gearbox cases (declining usage). It is resistant to destruction and weakening by oxidation (rust).

Production[link]

Cast iron is made by re-melting pig iron, often along with substantial quantities of scrap iron, scrap steel, lime stone, carbon(coke) and taking various steps to remove undesirable contaminants. Phosphorus and sulphur may be burnt out of the molten iron, but this also burns out the carbon, which must be replaced. Depending on the application, carbon and silicon content are adjusted to the desired levels, which may be anywhere from 2 to 3.5% and 1 to 3% respectively. Other elements are then added to the melt before the final form is produced by casting.^{[citation needed]}

Iron is sometimes melted in a special type of blast furnace known as a cupola, but more often melted in electric induction furnaces or electric arc furnaces.^{[citation needed]} After melting is complete, the molten iron is poured into a holding furnace or ladle.

Production in the World[link]

World cast iron production in 2009 was 898,261 mln ton (that 3,2% lower than in 2008 - 927,123 mln ton)^[1].

World's top-10 cast iron producers (in mln ton) are:

1	China	543,748
2	Japan	66,943
3	Russia	43,945
4	India	29,646
5	South Korea	27,278
6	Ukraine	25,676
7	Brazil	25,267
8	Germany	20,154
9	United States	18,936
10	France	8,105

Types[link]

Cast iron drain, waste and vent piping

Cast iron plate on grand piano

Alloying elements[link]

Cast iron's properties are changed by adding various alloying elements, or alloyants. Next to carbon, silicon is the most important alloyant because it forces carbon out of solution. Instead the carbon forms graphite which results in a softer iron, reduces shrinkage, lowers strength, and decreases density. Sulfur, when added, forms iron sulfide, which prevents the formation of graphite and increases hardness. The problem with sulfur is that it makes molten cast iron sluggish, which causes short run defects. To counter the effects of sulfur, manganese is added because the two form into manganese sulfide instead of iron sulfide. The manganese sulfide is lighter than the melt so it tends to float out of the melt and into the slag. The amount of manganese required to neutralize sulfur is 1.7×sulfur content+0.3%. If more than this amount of manganese is added, then manganese carbide forms, which increases hardness and chilling, except in grey iron, where up to 1% of manganese increases strength and density.^[2]

Nickel is one of the most common alloyants because it refines the pearlite and graphite structure, improves toughness, and evens out hardness differences between section thicknesses. Chromium is added in small amounts to the ladle to reduce free graphite, produce chill, and because it is a powerful carbide stabilizer; nickel is often added in conjunction. A small amount of tin can be added as a substitute for 0.5% chromium. Copper is added in the ladle or in the furnace, on the order of 0.5 to 2.5%, to decrease chill, refine graphite, and increase fluidity. Molybdenum is added on the order of 0.3 to 1% to increase chill and refine the graphite and pearlite structure; it is often added in conjunction with nickel, copper, and chromium to form high strength irons. Titanium is added as a degasser and deoxidizer, but it also increases fluidity. 0.15 to 0.5% vanadium are added to cast iron to stabilize cementite, increase hardness, and increase resistance to wear and heat. 0.1 to 0.3% zirconium helps to form graphite, deoxidize, and increase fluidity.^[2]

In malleable iron melts, bismuth is added, on the scale of 0.002 to 0.01%, to increase how much silicon can be added. In white iron, boron is added to aid in the production of malleable iron; it also reduces the coarsening effect of bismuth.^[2]

Grey cast iron[link]

Grey cast iron is characterized by its graphitic microstructure, which causes fractures of the material to have a grey appearance. It is the most commonly used cast iron and the most widely used cast material based on weight. Most cast irons have a chemical composition of 2.5 to 4.0% carbon, 1 to 3% silicon, and the remainder is iron. Grey cast iron has less tensile strength and shock resistance than steel, but its compressive strength is comparable to low and medium carbon steel.

[edit] White cast iron

It is the iron that displays white fractured surface due to the presence of cementite. With a lower silicon content and faster cooling, the carbon in white cast iron precipitates out of the melt as the metastable phase cementite, Fe₃C, rather than graphite. The cementite which precipitates from the melt forms as relatively large particles, usually in a eutectic mixture, where the other phase is austenite (which on cooling might transform to martensite). These eutectic carbides are much too large to provide precipitation hardening (as in some steels, where cementite precipitates might inhibit plastic deformation by impeding the movement of dislocations through the ferrite matrix). Rather, they increase the bulk hardness of the cast iron simply by virtue of their own very high hardness and their substantial volume fraction, such that the bulk hardness can be approximated by a rule of mixtures. In any case, they offer hardness at the expense of toughness. Since carbide makes up a large fraction of the material, white cast iron could reasonably be classified as a cermet. White iron is too brittle for use in many structural components, but with good hardness and abrasion resistance and relatively low cost, it finds use in such applications as the wear surfaces (impeller and volute) of slurry pumps, shell liners and lifter bars in ball mills and autogenous grinding mills, balls and rings in coal pulverisers, and the teeth of a backhoe's digging bucket (although cast medium-carbon martensitic steel is more common for this application).

It is difficult to cool thick castings fast enough to solidify the melt as white cast iron all the way through. However, rapid cooling can be used to solidify a shell of white cast iron, after which the remainder cools more slowly to form a core of grey cast iron. The resulting casting, called a chilled casting, has the benefits of a hard surface and a somewhat tougher interior.

High-chromium white iron alloys allow massive castings (for example, a 10-tonne impeller) to be sand cast, i.e., a high cooling rate is not required, as well as providing impressive abrasion resistance.^{[citation needed]}

Malleable cast iron[link]

Malleable iron starts as a white iron casting that is then heat treated at about 900 °C (1,650 °F). Graphite separates out much more slowly in this case, so that surface tension has time to form it into spheroidal particles rather than flakes. Due to their lower aspect ratio, spheroids are relatively short and far from one another, and have a lower cross section vis-a-vis a propagating crack or phonon. They also have blunt boundaries, as opposed to flakes, which alleviates the stress concentration problems faced by grey cast iron. In general, the properties of malleable cast iron are more like mild steel. There is a limit to how large a part can be cast in malleable iron, since it is made from white cast iron.

Ductile cast iron[link]

A more recent development is nodular or ductile cast iron. Tiny amounts of magnesium or cerium added to these alloys slow down the growth of graphite precipitates by bonding to the edges of the graphite planes. Along with careful control of other elements and timing, this allows the carbon to separate as spheroidal particles as the material solidifies. The properties are similar to malleable iron, but parts can be cast with larger sections.

Table of comparative qualities of cast irons[link]

Historical uses[link]

Because cast iron is comparatively brittle, it is not suitable for purposes where a sharp edge or flexibility is required. It is strong under compression, but not under tension. Cast Iron was first invented in China in the 4th century BC (see also: Du Shi) and poured into moulds to make ploughshares and pots as well as weapons and pagodas.^[4] In the west, where it did not become available till the late 14th century, its earliest uses included cannon and shot. Henry VIII initiated the casting of cannon in England. Soon, English iron workers using blast furnaces developed the technique of producing cast iron cannons, which, while heavier than the prevailing bronze cannons, were much cheaper and enabled England to arm her navy better. The ironmasters of the Weald continued producing cast irons until the 1760s and armament was one of the main uses of irons after the Restoration.

Cast iron pots were made at many English blast furnaces at the time. In 1707, Abraham Darby patented a method of making pots (and kettles) thinner and hence cheaper than his rivals could. This meant that his Coalbrookdale furnaces became dominant as suppliers of pots, an activity in which they were joined in the 1720s and 1730s by a small number of other coke-fired blast furnaces.

The development of the steam engine by Thomas Newcomen provided further market for cast iron, since cast iron was considerably cheaper than the brass of which the engine cylinders were originally made. John Wilkinson was a great exponent of cast iron, who, amongst other things, cast the cylinders for many of James Watt's improved steam engines until the establishment of the Soho Foundry in 1795.

Cast iron bridges[link]

The use of cast iron for structural purposes began in the late 1770s, when Abraham Darby III built the Iron Bridge, although short beams had already been used, such as in the blast furnaces at Coalbrookdale. Other inventions followed, including one patented by Thomas Paine. Cast iron bridges became commonplace as the Industrial Revolution gathered pace. Thomas Telford adopted the material for his bridge upstream at Buildwas, and then for a canal trough aqueduct at Longdon-on-Tern on the Shrewsbury Canal.

It was followed by the Chirk Aqueduct and the Pontcysyllte Aqueduct, both of which remain in use following the recent restorations. Cast iron beam bridges were used widely by the early railways, such as the Water Street Bridge at the Manchester terminus of the Liverpool and Manchester Railway. Problems arose when a new bridge carrying the Chester and Holyhead Railway across the River Dee in Chester collapsed in May 1847, less than a year after it was opened. The Dee bridge disaster was caused by excessive loading at the centre of the beam by a passing train, and many similar bridges had to be demolished and rebuilt, often in wrought iron. The bridge had been erroneously designed, being trussed with wrought iron straps, which were wrongly thought to reinforce the structure. The centres of the beams were put into bending, with the lower edge in tension, where cast iron, like masonry, is very weak.

The best way of using cast iron for bridge construction was by using arches, so that all the material is in compression. Cast iron, again like masonry, is very strong in compression. Wrought iron, like most other kinds of iron and indeed like most metals in general, is strong in tension, and also tough - resistant to fracturing. The relationship between wrought iron and cast iron, for structural purposes, may be thought of as analogous to the relationship between wood and stone.

Nevertheless, cast iron continued to be used in inappropriate structural ways, until the Tay Rail Bridge disaster of 1879 cast serious doubt on the use of the material. Crucial lugs for holding tie bars and struts in the Tay Bridge had been cast integral with the columns and they failed in the early stages of the accident. In addition, the bolt holes were also cast and not drilled, so that all the tension from the tie bars was placed on a corner, rather than being spread over the length of the hole. The replacement bridge was built in wrought iron and steel.

Further bridge collapses occurred, however, culminating in the Norwood Junction rail accident of 1891. Thousands of cast iron rail underbridges were eventually replaced by steel equivalents.

• 

  Original Tay Bridge from the north

• 

  Fallen Tay Bridge from the north

• 

  The iron bridge over the River Severn at Coalbrookdale, England

• 

  The Eglinton Tournament Bridge, North Ayrshire, Scotland, built from cast iron

Buildings[link]

Cast iron columns enabled architects to build tall buildings without the enormously thick walls required to construct masonry buildings of any height. Such flexibility allowed tall buildings to have large windows. In urban centres like SoHo-Cast Iron Historic District in New York City, manufacturing buildings and early department stores were built with cast iron columns to allow daylight to enter. Slender cast iron columns could also support the weight that would otherwise require thick masonry columns or piers, opening up floor spaces in factories, and sight lines in churches and auditoriums. The historic Iron Building in Watervliet, New York, is a cast iron building.

Textile mills[link]

Another important use was in textile mills. The air in the mills contained flammable fibres from the cotton, hemp, or wool being spun. As a result, textile mills had an alarming propensity to burn down. The solution was to build them completely of non-combustible materials, and it was found convenient to provide the building with an iron frame, largely of cast iron, replacing flammable wood. The first such building was at Ditherington in Shrewsbury, Shropshire. Many other warehouses were built using cast iron columns and beams, although faulty designs, flawed beams or overloading sometimes caused building collapses and structural failures.

During the Industrial Revolution, cast iron was also widely used for frame and other fixed parts of machinery, including spinning and later weaving machines in textile mills. Cast iron became widely used, and many towns had foundries producing industrial and agricultural machinery.

See also[link]

• Cast-iron architecture
• Cast-iron cookware
• Meehanite
• Sand casting

References[link]

Further reading[link]

• John Gloag and Derek Bridgwater, A History of Cast Iron in Architecture, Allen and Unwin, London (1948)
• Peter R Lewis, Beautiful Railway Bridge of the Silvery Tay: Reinvestigating the Tay Bridge Disaster of 1879, Tempus (2004) ISBN 0-7524-3160-9
• Peter R Lewis, Disaster on the Dee: Robert Stephenson's Nemesis of 1847, Tempus (2007) ISBN 978-0-7524-4266-2
• George Laird, Richard Gundlach and Klaus Röhrig, Abrasion-Resistant Cast Iron Handbook, ASM International (2000) ISBN 0-87433-224-9

External links[link]

Wikimedia Commons has media related to: Cast iron

• Metallurgy of Cast Irons, Cambridge University
• Paper on the Tay bridge disaster
• Cast Iron In China and Europe

Look up cast in Wiktionary, the free dictionary.

Cast may refer to:

• Cast member, (c.1631) a group of performers in a play, movie, or performing arts
• Orthopedic cast, a protective shell which is used to help heal broken bones by holding the limb in place
• In archaeology, a cavity formed by the decomposition of wood furnishings or human or animal remains, previously covered due to volcanic ash fall
• The casting of magic spells
• In falconry, flying two or more falconry birds together
• In computer science, a typecast is a programming language method for changing data types
• Plaster cast, a copy made in plaster of another three-dimensional form, for example a sculpture

In music[link]

• Cast (band), an English alternative rock band
• Cast (Mexican band), a progressive Mexican rock band

Other[link]

• Cast, Finistère, a commune of the Finistère département, in France
• Cast (earthworm), mineral-rich organic matter that is excreted by earthworms
• Urinary cast, tubules found in urine
• Cast (archery), the distance a bow can shoot its arrow

See also[link]

• Caste, social division in society
• Casting (disambiguation)

This disambiguation page lists articles associated with the same title. If an internal link led you here, you may wish to change the link to point directly to the intended article.

manganese ← iron → cobalt - ↑ Fe ↓ Ru 26Fe Periodic table
Appearance
lustrous metallic with a grayish tinge Spectral lines of iron
General properties
Name, symbol, number	iron, Fe, 26
Pronunciation	/ˈaɪ.ərn/
Element category	transition metal
Group, period, block	8, 4, d
Standard atomic weight	55.845(2)
Electron configuration	[Ar] 3d6 4s2
Electrons per shell	2, 8, 14, 2 (Image)
Physical properties
Phase	solid
Density (near r.t.)	7.874 g·cm−3
Liquid density at m.p.	6.98 g·cm−3
Melting point	1811 K, 1538 °C, 2800 °F
Boiling point	3134 K, 2862 °C, 5182 °F
Heat of fusion	13.81 kJ·mol−1
Heat of vaporization	340 kJ·mol−1
Molar heat capacity	25.10 J·mol−1·K−1
Vapor pressure
P (Pa) 1 10 100 1 k 10 k 100 k at T (K) 1728 1890 2091 2346 2679 3132
Atomic properties
Oxidation states	8,[1] 7,[1] 6, 5[2], 4, 3, 2, 1[3], -1, -2 (amphoteric oxide)
Electronegativity	1.83 (Pauling scale)
Ionization energies (more)	1st: 762.5 kJ·mol−1
	2nd: 1561.9 kJ·mol−1
	3rd: 2957 kJ·mol−1
Atomic radius	126 pm
Covalent radius	132±3 (low spin), 152±6 (high spin) pm
Miscellanea
Crystal structure	body-centered cubic a=286.65 pm; face-centered cubic between 1185–1667 K
Magnetic ordering	ferromagnetic
	1043 K
Electrical resistivity	(20 °C) 96.1 nΩ·m
Thermal conductivity	80.4 W·m−1·K−1
Thermal expansion	(25 °C) 11.8 µm·m−1·K−1
Speed of sound (thin rod)	(r.t.) (electrolytic) 5120 m·s−1
Young's modulus	211 GPa
Shear modulus	82 GPa
Bulk modulus	170 GPa
Poisson ratio	0.29
Mohs hardness	4
Vickers hardness	608 MPa
Brinell hardness	490 MPa
CAS registry number	7439-89-6
Most stable isotopes
Main article: Isotopes of iron
iso NA half-life DM DE (MeV) DP 54Fe 5.8% >3.1×1022y 2ε capture  ? 54Cr 55Fe syn 2.73 y ε capture 0.231 55Mn 56Fe 91.72% 56Fe is stable with 30 neutrons 57Fe 2.2% 57Fe is stable with 31 neutrons 58Fe 0.28% 58Fe is stable with 32 neutrons 59Fe syn 44.503 d β− 1.565 59Co 60Fe syn 2.6×106 y β− 3.978 60Co
v t e · r

Iron (/ˈaɪərn/ EYE-ər-n) is a chemical element with the symbol Fe (from Latin: ferrum) and atomic number 26. It is a metal in the first transition series. It is the most common element (by mass) forming the planet Earth as a whole, forming much of Earth's outer and inner core. It is the fourth most common element in the Earth's crust. Iron's very common presence in rocky planets like Earth is due to its abundant production as a result of fusion in high-mass stars, where the production of nickel-56 (which decays to the most common isotope of iron) is the last nuclear fusion reaction that is exothermic. This causes radioactive nickel to become the last element to be produced before collapse of a supernova leads to the explosive events that scatter this precursor radionuclide of iron abundantly into space.

Like other group 8 elements, iron exists in a wide range of oxidation states, −2 to +8, although +2 and +3 are the most common. Elemental iron occurs in meteoroids and other low oxygen environments, but is reactive to oxygen and water. Fresh iron surfaces appear lustrous silvery-gray, but oxidize in normal air to give iron oxides, also known as rust. Unlike many other metals which form passivating oxide layers, iron oxides occupy more volume than iron metal, and thus iron oxides flake off and expose fresh surfaces for corrosion.

Iron metal has been used since ancient times, though lower-melting copper alloys were used first in history. Pure iron is soft (softer than aluminium), but is unobtainable by smelting. The material is significantly hardened and strengthened by impurities from the smelting process, such as carbon. A certain proportion of carbon (between 0.2% and 2.1%) produces steel, which may be up to 1000 times harder than pure iron. Crude iron metal is produced in blast furnaces, where ore is reduced by coke to cast iron, which has a high carbon content. Further refinement with oxygen reduces the carbon content to the correct proportion to make steel. Steels and low carbon iron alloys with other metals (alloy steels) are by far the most common metals in industrial use, due to their great range of desirable properties.

Iron chemical compounds, which include ferrous and ferric compounds, have many uses. Iron oxide mixed with aluminium powder can be ignited to create a thermite reaction, used in welding and purifying ores. It forms binary compounds with the halogens and the chalcogens. Among its organometallic compounds is ferrocene, the first sandwich compound discovered.

Iron plays an important role in biology, forming complexes with molecular oxygen in hemoglobin and myoglobin; these two compounds are common oxygen transport proteins in vertebrates. Iron is also the metal used at the active site of many important redox enzymes dealing with cellular respiration and oxidation and reduction in plants and animals.

Characteristics[link]

Mechanical properties[link]

The mechanical properties of iron and its alloys can be evaluated using a variety of tests, including the Brinell test, Rockwell test and the Vickers hardness test. The data on iron is so consistent that it is often used to calibrate measurements or to compare tests.^[5][6] However, the mechanical properties of iron are significantly affected by the sample's purity: pure research-purpose single crystals of iron are actually softer than aluminium,^[4] and the purest industrially produced iron (99.99%) has a hardness of 20–30 Brinell.^[7] An increase in the carbon content of the iron will initially cause a significant corresponding increase in the iron's hardness and tensile strength. Maximum hardness of 65 R_c is achieved with a 0.6% carbon content, although this produces a metal with a low tensile strength.^[8]

Phase diagram and allotropes[link]

Iron represents an example of allotropy in a metal. There are at least four allotropic forms of iron, known as α, γ, δ, and ε; at very high pressures, some controversial experimental evidence exists for a phase β stable at very high pressures and temperatures.^[9]

Low-pressure phase diagram of pure iron

As molten iron cools down it crystallizes at 1538 °C into its δ allotrope, which has a body-centered cubic (bcc) crystal structure. As it cools further its crystal structure changes to face-centered cubic (fcc) at 1394 °C, when it is known as γ-iron, or austenite. At 912 °C the crystal structure again becomes bcc as α-iron, or ferrite, is formed, and at 770 °C (the Curie point, T_c) iron becomes magnetic. As the iron passes through the Curie temperature there is no change in crystalline structure, but there is a change in "domain structure", where each domain contains iron atoms with a particular electronic spin. In unmagnetized iron, all the electronic spins of the atoms within one domain are in the same direction; the neighboring domains point in various directions and thus cancel out. In magnetized iron, the electronic spins of all the domains are aligned, so that the magnetic effects of neighboring domains reinforce each other. Although each domain contains billions of atoms, they are very small, about 10 micrometres across.^[10] At pressures above approximately 10 GPa and temperatures of a few hundred kelvin or less, α-iron changes into a hexagonal close-packed (hcp) structure, which is also known as ε-iron; the higher-temperature γ-phase also changes into ε-iron, but does so at higher pressure. The β-phase, if it exists, would appear at pressures of at least 50 GPa and temperatures of at least 1500 K; it has been thought to have an orthorhombic or a double hcp structure.^[9]

Iron is of greatest importance when mixed with certain other metals and with carbon to form steels. There are many types of steels, all with different properties, and an understanding of the properties of the allotropes of iron is key to the manufacture of good quality steels.

α-iron, also known as ferrite, is the most stable form of iron at normal temperatures. It is a fairly soft metal that can dissolve only a small concentration of carbon (no more than 0.021% by mass at 910 °C).^[11]

Above 912 °C and up to 1400 °C α-iron undergoes a phase transition from bcc to the fcc configuration of γ-iron, also called austenite. This is similarly soft and metallic but can dissolve considerably more carbon (as much as 2.04% by mass at 1146 °C). This form of iron is used in the type of stainless steel used for making cutlery, and hospital and food-service equipment.^[10]

The high-pressure phases of iron are important as endmember models for the solid parts of planetary cores. The inner core of the Earth is generally assumed to consist essentially of an iron-nickel alloy with ε (or β) structure.

The melting point of iron is experimentally well constrained for pressures up to approximately 50 GPa. For higher pressures, different studies placed the γ-ε-liquid triple point at pressures differing by tens of gigapascals and yielded differences of more than 1000 K for the melting point. Generally speaking, molecular dynamics computer simulations of iron melting and shock wave experiments suggest higher melting points and a much steeper slope of the melting curve than static experiments carried out in diamond anvil cells.^[12]

Isotopes[link]

Naturally occurring iron consists of four stable isotopes: 5.845% of ⁵⁴Fe, 91.754% of ⁵⁶Fe, 2.119% of ⁵⁷Fe and 0.282% of ⁵⁸Fe. Of these stable isotopes, only ⁵⁷Fe has a nuclear spin (−1/2). The nuclide ⁵⁴Fe is predicted to undergo double beta decay, but this process had never been observed experimentally for these nuclei, and only the lower limit on the half-life was established: t_1/2>3.1×10²² years.

⁶⁰Fe is an extinct radionuclide of long half-life (2.6 million years).^[13] It is not found on Earth, but its ultimate decay product is the stable nuclide nickel-60.

Much of the past work on measuring the isotopic composition of Fe has focused on determining ⁶⁰Fe variations due to processes accompanying nucleosynthesis (i.e., meteorite studies) and ore formation. In the last decade however, advances in mass spectrometry technology have allowed the detection and quantification of minute, naturally occurring variations in the ratios of the stable isotopes of iron. Much of this work has been driven by the Earth and planetary science communities, although applications to biological and industrial systems are beginning to emerge.^[14]

The most abundant iron isotope ⁵⁶Fe is of particular interest to nuclear scientists as it represents the most common endpoint of nucleosynthesis. It is often cited, falsely, as the isotope of highest binding energy, a distinction which actually belongs to nickel-62.^[15] Since ⁵⁶Ni is easily produced from lighter nuclei in the alpha process in nuclear reactions in supernovae (see silicon burning process), nickel-56 (14 alpha particles) is the endpoint of fusion chains inside extremely massive stars, since addition of another alpha particle would result in zinc-60, which requires a great deal more energy. This nickel-56, which has a half-life of about 6 days, is therefore made in quantity in these stars, but soon decays by two successive positron emissions within supernova decay products in the supernova remnant gas cloud, first to radioactive cobalt-56, and then stable iron-56. This last nuclide is therefore common in the universe, relative to other stable metals of approximately the same atomic weight.

In phases of the meteorites Semarkona and Chervony Kut a correlation between the concentration of ⁶⁰Ni, the daughter product of ⁶⁰Fe, and the abundance of the stable iron isotopes could be found which is evidence for the existence of ⁶⁰Fe at the time of formation of the Solar System. Possibly the energy released by the decay of ⁶⁰Fe contributed, together with the energy released by decay of the radionuclide ²⁶Al, to the remelting and differentiation of asteroids after their formation 4.6 billion years ago^{[citation needed]}. The abundance of ⁶⁰Ni present in extraterrestrial material may also provide further insight into the origin of the Solar System and its early history.

Nuclei of iron atoms have some of the highest binding energies per nucleon, surpassed only by the nickel isotope ⁶²Ni. This is formed by nuclear fusion in stars. Although a further tiny energy gain could be extracted by synthesizing ⁶²Ni, conditions in stars are unsuitable for this process to be favored. Elemental distribution on Earth greatly favors iron over nickel, and also presumably in supernova element production.^[16]

Iron-56 is the heaviest stable isotope produced by the alpha process in stellar nucleosynthesis; elements heavier than iron and nickel require a supernova for their formation. Iron is the most abundant element in the core of red giants, and is the most abundant metal in iron meteorites and in the dense metal cores of planets such as Earth.

Nucleosynthesis[link]

Iron is created by extremely large, extremely hot (over 2.5 billion kelvin) stars, through a process called the silicon burning process. It is the heaviest stable element to be produced in this manner. The process starts with the second largest stable nucleus created by silicon burning: calcium. One stable nucleus of calcium fuses with one helium nucleus, creating unstable titanium. Before the titanium decays, it can fuse with another helium nucleus, creating unstable chromium. Before the chromium decays, it can fuse with another helium nucleus, creating unstable iron. Before the iron decays, it can fuse with another helium nucleus, creating unstable nickel-56. Any further fusion of nickel-56 consumes energy instead of producing energy, so after the production of nickel-56, the star does not produce the energy necessary to keep the core from collapsing. Eventually, the nickel-56 decays to unstable cobalt-56 which, in turn decays to stable iron-56. When the core of the star collapses, it creates a Supernova. Supernovas also create additional forms of stable iron via the r-process.

Occurrence[link]

Planetary occurrence[link]

Iron meteorites of similar composition of Earth's inner and outer core

Iron is the sixth most abundant element in the Universe, and the most common refractory element.^[17] It is formed as the final exothermic stage of stellar nucleosynthesis, by silicon fusion in massive stars. Metallic iron is rarely found on the surface of the Earth because it tends to oxidize, but its oxides are pervasive and represent the primary ores. While it makes up about 5% of the Earth's crust, both the Earth's inner and outer core are believed to consist largely of an iron-nickel alloy constituting 35% of the mass of the Earth as a whole. Iron is consequently the most abundant element on Earth, but only the fourth most abundant element in the Earth's crust.^[18][19] Most of the iron in the crust is found combined with oxygen as iron oxide minerals such as hematite and magnetite. Large deposits of iron are found in banded iron formations. These geological formations are a type of rock consisting of repeated thin layers of iron oxides, either magnetite (Fe₃O₄) or hematite (Fe₂O₃), alternating with bands of iron-poor shale and chert. The banded iron formations are common in the time between 3,700 million years ago and 1,800 million years ago^[20][21]

About 1 in 20 meteorites consist of the unique iron-nickel minerals taenite (35–80% iron) and kamacite (90–95% iron). Although rare, iron meteorites are the main form of natural metallic iron on the Earth's surface.^[22] It was proven by Mössbauer spectroscopy that the red color of the surface of Mars is derived from an iron oxide-rich regolith.^[23]

Stocks in use in society[link]

According to the International Resource Panel's Metal Stocks in Society report, the global per capita stock of iron in use in society is 2200 kg. Much of this is in more-developed countries (7000–14000 kg per capita) rather than less-developed countries (2000 kg per capita).

Chemistry and compounds[link]

Iron forms compounds mainly in the +2 and +3 oxidation states. Traditionally, iron(II) compounds are called ferrous, and iron(III) compounds ferric. Iron also occurs in higher oxidation states, an example being the purple potassium ferrate (K₂FeO₄) which contains iron in its +6 oxidation state. Iron(IV) is a common intermediate in many in biochemical oxidation reactions.^[24][25] Numerous organometallic compounds contain formal oxidation states of +1, 0, −1, or even −2. The oxidation states and other bonding properties are often assessed using the technique of Mössbauer spectroscopy.^[26] There are also many mixed valence compounds that contain both iron(II) and iron(III) centers, such as magnetite and Prussian blue (Fe₄(Fe[CN]₆)₃).^[25] The latter is used as the traditional "blue" in blueprints.^[27]

Hydrated iron(III) chloride, also known as ferric chloride

The iron compounds produced on the largest scale in industry are iron(II) sulfate (FeSO₄·7H₂O) and iron(III) chloride (FeCl₃). The former is one of the most readily available sources of iron(II), but is less stable to aerial oxidation than Mohr's salt ((NH₄)₂Fe(SO₄)₂·6H₂O). Iron(II) compounds tend to be oxidized to iron(III) compounds in the air.^[25]

Unlike many other metals, iron does not form amalgams with mercury. As a result, mercury is traded in standardized 76 pound flasks (34 kg) made of iron.^[28]

Binary compounds[link]

Iron reacts with oxygen in the air to form various oxide and hydroxide compounds; the most common are iron(II,III) oxide (Fe₃O₄), and iron(III) oxide (Fe₂O₃). Iron(II) oxide also exists, though it is unstable at room temperature. These oxides are the principal ores for the production of iron (see bloomery and blast furnace). They are also used in the production of ferrites, useful magnetic storage media in computers, and pigments. The best known sulfide is iron pyrite (FeS₂), also known as fool's gold owing to its golden luster.^[25]

The binary ferrous and ferric halides are well known, with the exception of ferric iodide. The ferrous halides typically arise from treating iron metal with the corresponding binary halogen acid to give the corresponding hydrated salts.^[25]

Fe + 2 HX → FeX₂ + H₂

Iron reacts with fluorine, chlorine, and bromine to give the corresponding ferric halides, ferric chloride being the most common:

2 Fe + 3 X₂ → 2 FeX₃ (X = F, Cl, Br)

Coordination and organometallic compounds[link]

Prussian blue

Several cyanide complexes are known. The most famous example is Prussian blue, (Fe₄(Fe[CN]₆)₃). Potassium ferricyanide and potassium ferrocyanide are also known; the formation of Prussian blue upon reaction with iron(II) and iron(III) respectively forms the basis of a "wet" chemical test.^[25] Prussian blue is also used as an antidote for thallium and radioactive caesium poisoning.^[29][30] Prussian blue can be used in laundry bluing to correct the yellowish tint left by ferrous salts in water.^[31]

Ferrocene

Several carbonyl compounds of iron are known. The premier iron(0) compound is iron pentacarbonyl, Fe(CO)₅, which is used to produce carbonyl iron powder, a highly reactive form of metallic iron. Thermolysis of iron pentacarbonyl gives the trinuclear cluster, triiron dodecacarbonyl. Collman's reagent, disodium tetracarbonylferrate, is a useful reagent for organic chemistry; it contains iron in the −2 oxidation state. Cyclopentadienyliron dicarbonyl dimer contains iron in the rare +1 oxidation state.^[32]

Ferrocene is an extremely stable complex. The first sandwich compound, it contains an iron(II) center with two cyclopentadienyl ligands bonded through all ten carbon atoms. This arrangement was a shocking novelty when it was first discovered,^[33] but the discovery of ferrocene has led to a new branch of organometallic chemistry. Ferrocene itself can be used as the backbone of a ligand, e.g. dppf. Ferrocene can itself be oxidized to the ferrocenium cation (Fc⁺); the ferrocene/ferrocenium couple is often used as a reference in electrochemistry.^[34]

History[link]

Wrought iron[link]

The symbol for Mars has been used since antiquity to represent iron.

The Delhi iron pillar is an example of the iron extraction and processing methodologies of India. The iron pillar at Delhi has withstood corrosion for the last 1600 years.

Iron objects of great age are much rarer than objects made of gold or silver due to the ease of corrosion of iron.^[35] Beads made of meteoric iron in 3500 B.C. or earlier were found in Gerzah, Egypt by G. A. Wainwright.^[36] The beads contain 7.5% nickel, which is a signature of meteoric origin since iron found in the Earth's crust has very little to no nickel content. Meteoric iron was highly regarded due to its origin in the heavens and was often used to forge weapons and tools or whole specimens placed in churches.^[36] Items that were likely made of iron by Egyptians date from 2500 to 3000 BC.^[35] Iron had a distinct advantage over bronze in warfare implements. It was much harder and more durable than bronze, although susceptible to rust. However, this is contested. Hittitologist Trevor Bryce argues that before advanced iron-working techniques were developed in India, cast-iron weapons used by early Mesopotamian armies had a tendency to shatter in combat, due to their high carbon content.^[37]

The first iron production started in the Middle Bronze Age but it took several centuries before iron displaced bronze. Samples of smelted iron from Asmar, Mesopotamia and Tall Chagar Bazaar in northern Syria were made sometime between 2700 and 3000 BC.^[38] The Hittites appear to be the first to understand the production of iron from its ores and regard it highly in their society.^[31] They began to smelt iron between 1500 and 1200 BC and the practice spread to the rest of the Near East after their empire fell in 1180 BC.^[38] The subsequent period is called the Iron Age. Iron smelting, and thus the Iron Age, reached Europe two hundred years later and arrived in Zimbabwe, Africa by the 8th century.^[38]

Artifacts from smelted iron occur in India from 1800 to 1200 BC,^[39] and in the Levant from about 1500 BC (suggesting smelting in Anatolia or the Caucasus).^[40][41]

The Book of Genesis, fourth chapter, verse 22 contains the first mention of iron in the Old Testament of the Bible; "Tubal-cain, an instructor of every artificer in brass and iron."^[35] Other verses allude to iron mining (Job 28:2), iron used as a stylus (Job 19:24), furnace (Deuteronomy 4:20), chariots (Joshua 17:16), nails (I Chron. 22:3), saws and axes (II Sam. 12:31), and cooking utensils (Ezekiel 4:3).^[42] The metal is also mentioned in the New Testament, for example in Acts chapter 12 verse 10, "[Peter passed through] the iron gate that leadeth unto the city" of Antioch.^[43] The Quran referred to Iron 1400 years ago.

Iron working was introduced to Greece in the late 11th century BC.^[44] The spread of ironworking in Central and Western Europe is associated with Celtic expansion. According to Pliny the Elder, iron use was common in the Roman era.^[36] The annual iron output of the Roman Empire is estimated at 84,750 t,^[45] while the similarly populous Han China produced around 5,000 t.^[46]

During the Industrial Revolution in Britain, Henry Cort began refining iron from pig iron to wrought iron (or bar iron) using innovative production systems. In 1783 he patented the puddling process for refining iron ore. It was later improved by others including Joseph Hall.

Cast iron[link]

Cast iron was first produced in China about 550 BC,^[47] but was hardly in Europe until the medieval period.^[48][49] During the medieval period, means were found in Europe of producing wrought iron from cast iron (in this context known as pig iron) using finery forges. For all these processes, charcoal was required as fuel.

Coalbrookdale by Night, 1801. Blast furnaces light the iron making town of Coalbrookdale.

Medieval blast furnaces were about 10 feet (3.0 m) tall and made of fireproof brick; forced air was usually provided by hand-operated bellows.^[49] Modern blast furnaces have grown much bigger.

In 1709, Abraham Darby I established a coke-fired blast furnace to produce cast iron. The ensuing availability of inexpensive iron was one of the factors leading to the Industrial Revolution. Toward the end of the 18th century, cast iron began to replace wrought iron for certain purposes, because it was cheaper. Carbon content in iron wasn't implicated as the reason for the differences in properties of wrought iron, cast iron and steel until the 18th century.^[38]

Since iron was becoming cheaper and more plentiful, it also became a major structural material following the building of the innovative first iron bridge in 1778.

Steel[link]

Steel (with smaller carbon content than pig iron but more than wrought iron) was first produced in antiquity by using a bloomery. Blacksmiths in Luristan in western Iran were making good steel by 1000 BC.^[38] Then improved versions, Wootz steel by India and Damascus steel by China were developed around 300 B.C. and 500 A.D. respectively. These methods were specialized, and so steel did not become a major commodity until the 1850s.^[50]

New methods of producing it by carburizing bars of iron in the cementation process were devised in the 17th century AD. In the Industrial Revolution, new methods of producing bar iron without charcoal were devised and these were later applied to produce steel. In the late 1850s, Henry Bessemer invented a new steelmaking process, involving blowing air through molten pig iron, to produce mild steel. This made steel much more economical, thereby leading to wrought iron no longer being produced.^{[citation needed]}

Foundations of modern chemistry[link]

Antoine Lavoisier used the reaction of water steam with metallic iron inside an incandescent iron tube to produce hydrogen in his experiments leading to the demonstration of the mass conservation. Anaerobic oxidation of iron at high temperature can be schematically represented by the following reactions:

   Fe +    H₂O → FeO + H₂

2 Fe + 3 H₂O → Fe₂O₃ + 3 H₂

3 Fe + 4 H₂O → Fe₃O₄ + 4 H₂

Recent discoveries[link]

• discovery of Mössbauer effect
• many enzymes use iron in the catalytic center
• Nickel-56 is the natural end product of silicon burning in massive stars. However Nickel-56 decays to cobalt-56 and then to stable iron-56, ultimately making iron the most abundant heavy element produced by that nucleosynthesis.^[51]
• superconductivity?
• magnetic effect
• ferrocene

Industrial production[link]

The production of iron or steel is a process containing two main stages, unless the desired product is cast iron. The first stage is to produce pig iron in a blast furnace. Alternatively, it may be directly reduced. The second is to make wrought iron or steel from pig iron by a further process.

The fining process of smelting iron ore to make wrought iron from pig iron, with the right illustration displaying men working a blast furnace, from the Tiangong Kaiwu encyclopedia, published in 1637 by Song Yingxing.

How iron was extracted in the 19th century

For a few limited purposes like electromagnet cores, pure iron is produced by electrolysis of a ferrous sulfate solution^[31]

Blast furnace[link]

Ninety percent of all mining of metallic ores is for the extraction of iron^{[citation needed]}. Industrially, iron production involves iron ores, principally hematite (nominally Fe₂O₃) and magnetite (Fe₃O₄) in a carbothermic reaction (reduction with carbon) in a blast furnace at temperatures of about 2000 °C. In a blast furnace, iron ore, carbon in the form of coke, and a flux such as limestone (which is used to remove silicon dioxide impurities in the ore which would otherwise clog the furnace with solid material) are fed into the top of the furnace, while a massive blast of heated air, about 4 tons per ton of iron,^[49] is forced into the furnace at the bottom.

Iron output in 2005

In the furnace, the coke reacts with oxygen in the air blast to produce carbon monoxide:

2 C + O₂ → 2 CO

The carbon monoxide reduces the iron ore (in the chemical equation below, hematite) to molten iron, becoming carbon dioxide in the process:

Fe₂O₃ + 3 CO → 2 Fe + 3 CO₂

Some iron in the high-temperature lower region of the furnace reacts directly with the coke:

2 Fe₂O₃ + 3 C → 4 Fe + 3 CO₂

The flux is present to melt impurities in the ore, principally silicon dioxide sand and other silicates. Common fluxes include limestone (principally calcium carbonate) and dolomite (calcium-magnesium carbonate). Other fluxes may be used depending on the impurities that need to be removed from the ore. In the heat of the furnace the limestone flux decomposes to calcium oxide (also known as quicklime):

CaCO₃ → CaO + CO₂

Then calcium oxide combines with silicon dioxide to form a liquid slag.

CaO + SiO₂ → CaSiO₃

The slag melts in the heat of the furnace. In the bottom of the furnace, the molten slag floats on top of the denser molten iron, and apertures in the side of the furnace are opened to run off the iron and the slag separately. The iron, once cooled, is called pig iron, while the slag can be used as a material in road construction or to improve mineral-poor soils for agriculture^[49]

This heap of iron ore pellets will be used in steel production.

In 2005, approximately 1,544 million metric tons of iron ore were produced worldwide. According to the British Geological Survey, China was the top producer of iron ore with at least one quarter world share, followed by Brazil, Australia and India.

Direct iron reduction[link]

Since coke is becoming more regulated due to environmental concerns, alternative methods of processing iron have been developed. One of them is known as direct iron reduction.^[49] It reduces iron ore to a powder substance called sponge iron, which is suitable for steelmaking. There are two main reactions that go on in the direct reduction process:

Natural gas is partially oxidized (with heat and a catalyst):

2 CH₄ + O₂ → 2 CO + 4 H₂

These gases are then treated with iron ore in a furnace, producing solid sponge iron:

Fe₂O₃ + CO + 2 H₂ → 2 Fe + CO₂ + 2 H₂O

Silica is removed by adding a flux, i.e. limestone, later.

Further processes[link]

Iron-carbon phase diagram, various stable solid solution forms

Pig iron is not pure iron, but has 4–5% carbon dissolved in it with small amounts of other impurities like sulfur, magnesium, phosphorus and manganese. As the carbon is the major impurity, the iron (pig iron) becomes brittle and hard. This form of iron, also known as cast iron, is used to cast articles in foundries such as stoves, pipes, radiators, lamp-posts and rails.

Alternatively pig iron may be made into steel (with up to about 2% carbon) or wrought iron (commercially pure iron). Various processes have been used for this, including finery forges, puddling furnaces, Bessemer converters, open hearth furnaces, basic oxygen furnaces, and electric arc furnaces. In all cases, the objective is to oxidize some or all of the carbon, together with other impurities. On the other hand, other metals may be added to make alloy steels.

The hardness of the steel depends upon its carbon content: the higher the percentage of carbon, the greater the hardness and the lesser the malleability. The properties of the steel can also be changed by several methods.

Annealing involves the heating of a piece of steel to 700–800 °C for several hours and then gradual cooling. It makes the steel softer and more workable.

Steel may be hardened by cold working. The metal is bent or hammered into its final shape at a relatively cool temperature. Cold forging is the stamping of a piece of steel into shape by a heavy press. Wrenches are commonly made by cold forging. Cold rolling, which involves making a thinner but harder sheet, and cold drawing, which makes a thinner but stronger wire, are two other methods of cold working. To harden the steel, it is heated to red-hot and then cooled by quenching it in the water. It becomes harder and more brittle. If it is too hardened, it is then heated to a required temperature and allowed to cool. The steel thus formed is less brittle.

Heat treatment is another way to harden steel. The steel is heated red-hot, then cooled quickly. The iron carbide molecules are decomposed by the heat, but do not have time to reform. Since the free carbon atoms are stuck, it makes the steel much harder and stronger than before.^[49]

Sometimes both toughness and hardness are desired. A process called case hardening may be used. Steel is heated to about 900 °C then plunged into oil or water. Carbon from the oil can diffuse into the steel, making the surface very hard. The surface cools quickly, but the inside cools slowly, making an extremely hard surface and a durable, resistant inner layer.

Iron may be passivated by dipping it into a concentrated nitric acid solution. This forms a protective layer of oxide on the metal, protecting it from further corrosion.^[52]

Applications[link]

Metallurgical[link]

Photon mass attenuation coefficient for iron.

Iron is the most widely used of all the metals, accounting for 95% of worldwide metal production.^{[citation needed]} Its low cost and high strength make it indispensable in engineering applications such as the construction of machinery and machine tools, automobiles, the hulls of large ships, and structural components for buildings. Since pure iron is quite soft, it is most commonly used in the form of steel.

Commercially available iron is classified based on purity and the abundance of additives. Pig iron has 3.5–4.5% carbon^[53] and contains varying amounts of contaminants such as sulfur, silicon and phosphorus. Pig iron is not a saleable product, but rather an intermediate step in the production of cast iron and steel from iron ore. Cast iron contains 2–4% carbon, 1–6% silicon, and small amounts of manganese. Contaminants present in pig iron that negatively affect material properties, such as sulfur and phosphorus, have been reduced to an acceptable level. It has a melting point in the range of 1420–1470 K, which is lower than either of its two main components, and makes it the first product to be melted when carbon and iron are heated together. Its mechanical properties vary greatly, dependent upon the form carbon takes in the alloy.

"White" cast irons contain their carbon in the form of cementite, or iron carbide. This hard, brittle compound dominates the mechanical properties of white cast irons, rendering them hard, but unresistant to shock. The broken surface of a white cast iron is full of fine facets of the broken carbide, a very pale, silvery, shiny material, hence the appellation.

In gray iron the carbon exists free as fine flakes of graphite, and also renders the material brittle due to the stress-raising nature of the sharp edged flakes of graphite. A newer variant of gray iron, referred to as ductile iron is specially treated with trace amounts of magnesium to alter the shape of graphite to spheroids, or nodules, vastly increasing the toughness and strength of the material.

Wrought iron contains less than 0.25% carbon.^[53] It is a tough, malleable product, but not as fusible as pig iron. If honed to an edge, it loses it quickly. Wrought iron is characterized by the presence of fine fibers of slag entrapped in the metal. Wrought iron is more corrosion resistant than steel. It has been almost completely replaced by mild steel for traditional "wrought iron" products and blacksmithing.

Mild steel corrodes more readily than wrought iron, but is cheaper and more widely available. Carbon steel contains 2.0% carbon or less,^[54] with small amounts of manganese, sulfur, phosphorus, and silicon. Alloy steels contain varying amounts of carbon as well as other metals, such as chromium, vanadium, molybdenum, nickel, tungsten, etc. Their alloy content raises their cost, and so they are usually only employed for specialist uses. One common alloy steel, though, is stainless steel. Recent developments in ferrous metallurgy have produced a growing range of microalloyed steels, also termed 'HSLA' or high-strength, low alloy steels, containing tiny additions to produce high strengths and often spectacular toughness at minimal cost.

Apart from traditional applications, iron is also used for protection from ionizing radiation. Although it is lighter than another traditional protection material, lead, it is much stronger mechanically. The attenuation of radiation as a function of energy is shown in the graph.

The main disadvantage of iron and steel is that pure iron, and most of its alloys, suffer badly from rust if not protected in some way. Painting, galvanization, passivation, plastic coating and bluing are all used to protect iron from rust by excluding water and oxygen or by cathodic protection.

Of compounds[link]

Although its metallurgical role is dominant in terms of amounts, iron compounds are pervasive in industry as well being used in many niche uses. Iron catalysts are traditionally used in the Haber-Bosch Process for the production of ammonia and the Fischer-Tropsch process for conversion of carbon monoxide to hydrocarbons for fuels and lubricants.^[55] Powdered iron in an acidic solvent was used in the Bechamp reduction the reduction of nitrobenzene to aniline.^[56]

Iron(III) chloride finds use in water purification and sewage treatment, in the dyeing of cloth, as a coloring agent in paints, as an additive in animal feed, and as an etchant for copper in the manufacture of printed circuit boards.^[57] It can also be dissolved in alcohol to form tincture of iron.^[31] The other halides tend to be limited to laboratory uses.

Iron(II) sulfate is used as a precursor to other iron compounds. It is also used to reduce chromate in cement. It is used to fortify foods and treat iron deficiency anemia. These are its main uses. Iron(III) sulfate is used in settling minute sewage particles in tank water. Iron(II) chloride is used as a reducing flocculating agent, in the formation of iron complexes and magnetic iron oxides, and as a reducing agent in organic synthesis.

Biological role[link]

Iron is abundant in biology. Iron-proteins are found in all living organisms, ranging from the evolutionarily primitive archaea to humans. The color of blood is due to the hemoglobin, an iron-containing protein. As illustrated by hemoglobin, iron often is bound to cofactors, e.g. in hemes. The iron-sulfur clusters are pervasive and include nitrogenase, the enzymes responsible for biological nitrogen fixation. Influential theories of evolution have invoked a role for iron sulfides in the iron-sulfur world theory.

Structure of Heme b, in the protein additional ligand(s) would be attached to Fe.

Iron is a necessary trace element found in nearly all living organisms. Iron-containing enzymes and proteins, often containing heme prosthetic groups, participate in many biological oxidations and in transport. Examples of proteins found in higher organisms include hemoglobin, cytochrome (see high-valent iron), and catalase.^[58]

Bioinorganic compounds[link]

The most commonly-known and studied "bioinorganic" compounds of iron (i.e., iron compounds used in biology) are the heme proteins: examples are hemoglobin, myoglobin, and cytochrome P450. These compounds can transport gases, build enzymes, and be used in transferring electrons. Metalloproteins are a group of proteins with metal ion cofactors. Some examples of iron metalloproteins are ferritin and rubredoxin. Many enzymes vital to life contain iron, such as catalase, lipoxygenases, and IRE-BP.

Health and diet[link]

Iron is pervasive, but particularly rich sources of dietary iron include red meat, lentils, beans, poultry, fish, leaf vegetables, watercress, tofu, chickpeas, black-eyed peas, blackstrap molasses, fortified bread, and fortified breakfast cereals. Iron in low amounts is found in molasses, teff and farina. Iron in meat (heme iron) is more easily absorbed than iron in vegetables.^[59] Although some studies suggest that heme/hemoglobin from red meat has effects which may increase the likelihood of colorectal cancer,^[60][61] there is still some controversy,^[62] and even a few studies suggesting that there is not enough evidence to support such claims.^[63]

Iron provided by dietary supplements is often found as iron(II) fumarate, although iron sulfate is cheaper and is absorbed equally well. Elemental iron, or reduced iron, despite being absorbed at only one third to two thirds the efficiency (relative to iron sulfate),^[64] is often added to foods such as breakfast cereals or enriched wheat flour. Iron is most available to the body when chelated to amino acids^[65] and is also available for use as a common iron supplement. Often the amino acid chosen for this purpose is the cheapest and most common amino acid, glycine, leading to "iron glycinate" supplements.^[66] The Recommended Dietary Allowance (RDA) for iron varies considerably based on age, gender, and source of dietary iron (heme-based iron has higher bioavailability).^[67] Infants may require iron supplements if they are bottle-fed cow's milk.^[68] Blood donors and pregnant women are at special risk of low iron levels and are often advised to supplement their iron intake.^[69]

Uptake and storage[link]

Iron acquisition poses a problem for aerobic organisms, because ferric iron is poorly soluble near neutral pH. Thus, bacteria have evolved high-affinity sequestering agents called siderophores.^[70][71][72]

After uptake, in cells, iron storage is carefully regulated; "free" iron ions do not exist as such. A major component of this regulation is the protein transferrin, which binds iron ions absorbed from the duodenum and carries it in the blood to cells.^[73] In animals, plants, and fungi, iron is often the metal ion incorporated into the heme complex. Heme is an essential component of cytochrome proteins, which mediate redox reactions, and of oxygen carrier proteins such as hemoglobin, myoglobin, and leghemoglobin.

Inorganic iron contributes to redox reactions in the iron-sulfur clusters of many enzymes, such as nitrogenase (involved in the synthesis of ammonia from nitrogen and hydrogen) and hydrogenase. Non-heme iron proteins include the enzymes methane monooxygenase (oxidizes methane to methanol), ribonucleotide reductase (reduces ribose to deoxyribose; DNA biosynthesis), hemerythrins (oxygen transport and fixation in marine invertebrates) and purple acid phosphatase (hydrolysis of phosphate esters).

Iron distribution is heavily regulated in mammals, partly because iron ions have a high potential for biological toxicity.^[74]

Regulation of uptake[link]

Iron uptake is tightly regulated by the human body, which has no regulated physiological means of excreting iron. Only small amounts of iron are lost daily due to mucosal and skin epithelial cell sloughing, so control of iron levels is mostly by regulating uptake.^[75] Regulation of iron uptake is impaired in some people as a result of a genetic defect that maps to the HLA-H gene region on chromosome 6. In these people, excessive iron intake can result in iron overload disorders, such as hemochromatosis. Many people have a genetic susceptibility to iron overload without realizing it or being aware of a family history of the problem. For this reason, it is advised that people do not take iron supplements unless they suffer from iron deficiency and have consulted a doctor. Hemochromatosis is estimated to cause disease in between 0.3 and 0.8% of Caucasians.^[76]

MRI finds that iron accumulates in the hippocampus of the brains of those with Alzheimer's disease and in the substantia nigra of those with Parkinson disease.^[77]

Permeable reactive barriers[link]

Zero-valent iron is the main reactive material for permeable reactive barriers.^{[citation needed]}

Precautions[link]

NFPA 704
1 0 1
Fire diamond for powdered iron metal

Large amounts of ingested iron can cause excessive levels of iron in the blood. High blood levels of free ferrous iron react with peroxides to produce free radicals, which are highly reactive and can damage DNA, proteins, lipids, and other cellular components. Thus, iron toxicity occurs when there is free iron in the cell, which generally occurs when iron levels exceed the capacity of transferrin to bind the iron. Damage to the cells of the gastrointestinal tract can also prevent them from regulating iron absorption leading to further increases in blood levels. Iron typically damages cells in the heart, liver and elsewhere, which can cause significant adverse effects, including coma, metabolic acidosis, shock, liver failure, coagulopathy, adult respiratory distress syndrome, long-term organ damage, and even death.^[78] Humans experience iron toxicity above 20 milligrams of iron for every kilogram of mass, and 60 milligrams per kilogram is considered a lethal dose.^[79] Overconsumption of iron, often the result of children eating large quantities of ferrous sulfate tablets intended for adult consumption, is one of the most common toxicological causes of death in children under six.^[79] The Dietary Reference Intake (DRI) lists the Tolerable Upper Intake Level (UL) for adults as 45 mg/day. For children under fourteen years old the UL is 40 mg/day.

The medical management of iron toxicity is complicated, and can include use of a specific chelating agent called deferoxamine to bind and expel excess iron from the body.^[78][80]

See also[link]

Chemistry portal

• El Mutún in Bolivia, where 20% of the world's accessible iron is located.
• Iron fertilization – proposed fertilization of oceans to stimulate phytoplankton growth.
• Iron (metaphor)
• Iron in folklore
• List of countries by iron production
• Pelletising – process of creation of iron ore pellets.
• Rustproof iron

References[link]

Books[link]

• H. R. Schubert, History of the British Iron and Steel Industry ... to 1775 AD (Routledge, London, 1957)
• R. F. Tylecote, History of Metallurgy (Institute of Materials, London 1992).
• R. F. Tylecote, 'Iron in the Industrial Revolution' in J. Day and R. F. Tylecote, The Industrial Revolution in Metals (Institute of Materials 1991), 200–60.
• Weeks, Mary Elvira; Leichester, Henry M. (1968). "Elements Known to the Ancients". Discovery of the Elements. Easton, PA: Journal of Chemical Education. pp. 29–40. ISBN 0-7661-3872-0. LCCCN 68-15217. 

External links[link]

Look up iron in Wiktionary, the free dictionary.

Wikimedia Commons has media related to: Iron

• WebElements.com – Iron
• It's Elemental – Iron
• The Most Tightly Bound Nuclei
• Crystal structure of iron
• Chemistry in its element podcast (MP3) from the Royal Society of Chemistry's Chemistry World: Iron
• The periodic table of videos: Iron

vep:Raud