'Iron' (
IPA: ) is a
chemical element with the symbol 'Fe' () and
atomic number 26. Iron is a
group 8 and
period 4 metal. Iron is a lustrous, silvery soft metal. Iron and
nickel are notable for being the final elements produced by
stellar nucleosynthesis, and thus are the heaviest elements which do not require a
supernova or similarly cataclysmic event for formation. Iron and nickel are therefore the most abundant metals in metallic meteorites and in the dense-metal cores of planets such as Earth.
Characteristics
Iron is believed to be the tenth most
abundant element in the
universe, and the fourth most abundant in the Earth's crust. The concentration of iron in the various layers in the
structure of the Earth ranges from high (probably greater than 80%, perhaps even a nearly pure iron crystal) at the inner core, to only 5% in the outer crust. Iron is second in abundance to
aluminium among the metals and fourth in abundance in the crust. Iron is the most abundant element by mass of our entire planet, making up 35% of the mass of the Earth as a whole.
Iron is a
metal extracted from
iron ore, and is almost never found in the free elemental state. In order to obtain elemental iron, the impurities must be removed by chemical
reduction. Iron is the main component of
steel, and it is used in the production of
alloys or
solid solutions of various metals, as well as some non-metals, particularly
carbon. The many iron-carbon alloys, which have very different properties, are discussed in the article on
steel.
Nuclei of iron have some of the highest binding energies per nucleon, surpassed only by the
nickel isotope 62Ni. The universally most abundant of the highly stable nuclides is, however,
56Fe. 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 favoured, and iron abundance on Earth greatly favors iron over nickel, and also presumably in supernova element production. When a very large
star contracts at the end of its life, internal pressure and temperature rise, allowing the star to produce progressively heavier elements, despite these being less stable than the elements around mass number 60, known as the "iron group". This leads to a
supernova.
Iron (as Fe
2+, ferrous ion) is a necessary
trace element used by almost all living organisms, the only exceptions are a few prokaryotic organisms which live in iron-poor conditions (such as the
lactobacilli in iron-poor milk) which use manganese for catalysis, instead. Iron-containing enzymes, usually containing
heme prosthetic groups, participate in catalysis of oxidation reactions in biology, and in transport of a number of soluble gases. See
hemoglobin,
cytochrome, and
catalase.
Applications
Iron is the most used of all the metals, comprising 95% of all the metal tonnage produced worldwide. Its combination of low cost and high strength make it indispensable, especially in applications like
automobiles, the
hulls of large
ships, and structural components for
buildings.
Steel is the best known alloy of iron, and some of the forms that iron can take include:
★
Pig iron has 4% – 5% carbon and contains varying amounts of contaminants such as
sulfur,
silicon and
phosphorus. Its only significance is that of an intermediate step on the way from
iron ore to
cast iron and
steel.
★
Cast iron contains 2% – 4.0%
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
grey 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 grey 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.
★
Carbon steel contains between 0.4% and 1.5%
carbon, with small amounts of
manganese,
sulfur,
phosphorus, and
silicon.
★
Wrought iron contains less than 0.2% carbon. It is a tough, malleable product, not as fusible as pig iron. It has a very small amount of carbon, a few tenths of a percent. If honed to an edge, it loses it quickly. Wrought iron is characterised, especially in old samples, by the presence of fine 'stringers' or filaments of
slag entrapped in the metal. Wrought iron does not
rust particularly quickly when used outdoors. It has largely been replaced by
mild steel for "wrought iron" gates and
blacksmithing. Mild steel does not have the same corrosion resistance but is cheaper and more widely available.
★
Alloy steels contain varying amounts of carbon as well as other metals, such as
chromium,
vanadium,
molybdenum,
nickel,
tungsten, etc. They are used for structural purposes, as their alloy content raises their cost and necessitates justification of their use. 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.
★
Iron(III) oxides are used in the production of
magnetic storage media in computers. They are often mixed with other compounds, and retain their magnetic properties in solution.
The main drawback to iron and steel is that pure iron, and most of its alloys, suffer badly from
rust if not protected in some way.
Painting,
galvanization, plastic coating and
bluing are some techniques used to protect iron from rust by excluding
water and
oxygen or by sacrificial protection.
Iron is believed to be the critical missing nutrient in the ocean that limits the growth of
plankton. Experimental
iron fertilization of areas of the ocean using
iron(II) sulfate has proven successful in increasing plankton growth
[1][2][3]. Larger scaled efforts are being attempted with the hope that iron seeding and ocean plankton growth can remove
carbon dioxide from the atmosphere, thereby counteracting the
greenhouse effect that is generally agreed by climatologists to cause
global warming[4].
Iron compounds
:''See also .''
_chloride_hexahydrate.jpg)
Iron chloride hexahydrate
★ Iron(III) acetate (Fe(C
2H
3O
2)
3 is used in the
dyeing of
cloth.
★ Iron(III) ammonium oxalate (Fe(NH
4)
3(C
2O
4)
4) is used in
blueprints.
★ Iron(III) arsenate (FeAsO
4) is used in
insecticide.
★
Iron(III) chloride (FeCl
3) is used: 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 etching material for engravement,
photography and printed circuits.
★ Iron(III) chromate (Fe
2(CrO
4)
3) is used as a yellow pigment for
paints and
ceramic.
★
Iron(III) hydroxide (Fe(OH)
3) is used as a brown
pigment for
rubber and in water purification systems.
★
Iron(III) phosphate (FePO
4) is used in
fertilizer and as an
additive in human and animal food.
★
Iron(II) acetate (Fe(C
2H
3O
2)
2 is used in the dyeing of fabrics and
leather, and as a
wood preservative.
★
Iron(II) gluconate (Fe(C
6H
11O
7)
2) is used as a dietary supplement in
iron pills.
★ Iron(II) oxalate (FeC
2O
4) is used as yellow
pigment for
paints,
plastics,
glass and
ceramic, and in
photography.
★
Iron(II) sulfate (FeSO
4) is used in
water purification and sewage treatment systems, as a
catalyst in the production of
ammonia, as an ingredient in
fertilizer and
herbicide, as an
additive in animal feed, in
wood preservative and as an
additive to
flour to increase iron levels.
★ Iron-Fluorine complex (FeF
6)
3- is found in solutions containing both Fe(III)
ions and
fluoride ions.
Historical aspects
The first iron used by mankind, far back in prehistory, came from meteors. The
smelting of iron in
bloomeries probably began in
Anatolia or the
Caucasus in the second millennium BC or the latter part of the preceding one.
Cast iron was first produced in
China about 550 BC, but not in Europe until the medieval period. 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.
Steel (with a smaller carbon content than
pig iron but more than
wrought iron) was first produced in antiquity. 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 and other
19th century and later processes have led to
wrought iron no longer being produced.
Occurrence

The red appearance of this water is due to iron in the rocks.
Iron is one of the most common elements on Earth, making up about 5% of the Earth's crust. Most of this iron is found in various
iron oxides, such as the minerals
hematite,
magnetite, and
taconite. The
earth's core is believed to consist largely of a metallic iron-
nickel alloy. About 5% of the
meteorites similarly consist of iron-nickel alloy. Although rare, these are the major form of natural metallic iron on the earth's surface.
The reason for Mars's red colour is thought to be an iron-oxide-rich soil.
''See also .''
Production of iron from iron ore
Main articles: Blast furnace

How Iron was extracted in the 19th century

Iron output in 2005
Industrially, iron is produced starting from
iron ores, principally
haematite (nominally Fe
2O
3) and
magnetite (Fe
3O
4) by 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 impurities in the ore which would otherwise clog the furnace with solid material) are fed into the top of the furnace, while a blast of heated
air is forced into the furnace at the bottom.
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:
:3
CO +
Fe2O3 → 2 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 (quicklime):
:
CaCO3 →
CaO +
CO2
Then calcium oxide combines with silicon dioxide to form a ''slag''.
:
CaO +
SiO2 →
CaSiO3
The slag melts in the heat of the furnace, which silicon dioxide would not have. In the bottom of the furnace, the molten slag floats on top of the more dense 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.
Pig iron is not pure iron, but has 4-5% carbon dissolved in it. This is subsequently reduced to
steel or commercially pure iron, known as
wrought iron, using other furnaces or converters.
In 2005, approximately 1,544Mt (million tons) of iron ore was produced worldwide. China was the top producer of iron ore with at least one-fourth world share followed by Brazil, Australia and India, reports the
British Geological Survey.
Isotopes
Naturally occurring iron consists of four
isotopes: 5.845% of radioactive
54Fe (half-life: >3.1×10
22 years), 91.754% of stable
56Fe, 2.119% of stable
57Fe and 0.282% of stable
58Fe.
60Fe is an extinct
radionuclide of long
half-life (1.5 million years).
Much of the past work on measuring the isotopic composition of Fe has centered 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.
[5]
The isotope
56Fe is of particular interest to nuclear scientists. A common misconception is that this isotope represents the most stable nucleus possible, and that it thus would be impossible to perform fission or fusion on
56Fe and still liberate energy. This is not true, as both
62Ni and
58Fe are more stable, being the most stable nuclei. However, since
56Fe is much more easily produced from lighter nuclei in nuclear reactions, it is the endpoint of fusion chains inside
extremely massive stars and is therefore common in the universe, relative to other
metals.
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. The abundance of
60Ni present in material may also provide further insight into the origin of the
solar system and its early history.
Of the stable isotopes, only
57Fe has a nuclear
spin (−1/2).
Iron in organic synthesis
The usage of iron metal filings in organic synthesis is mainly for the
reduction of
nitro compounds.
[6] Additionally, iron has been used for
desulfurizations
[7],
reduction of
aldehydes
[8], and the
deoxygenation of amine oxides
[9].
Iron in biology
Main articles: human iron metabolism
Iron is essential to nearly all known
organisms. In
cells, iron is generally stored in the centre of
metalloproteins, because "free" iron -- which binds non-specifically to many cellular components -- can catalyse production of toxic
free radicals.
In animals, plants, and fungi, iron is often 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 also 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 has a high potential for biological toxicity. Iron distribution is also regulated because many bacteria require iron, so restricting its availability to bacteria (generally by ing it inside cells) can help to prevent or limit infections. This is probably the reason for the relatively low amounts of iron in mammalian milk. A major component of this regulation is the protein
transferrin, which binds iron absorbed from the
duodenum and carries it in the
blood to cells.
[10]
Nutrition and dietary sources
Good sources of dietary iron include
red meat,
fish,
poultry,
lentils,
beans,
leaf vegetables,
tofu,
chickpeas,
black-eyed peas, potatoes with skin, bread made from completely whole-grain flour,
molasses,
teff and
farina. Iron in meat is more easily absorbed than iron in vegetables.
[11]
Iron provided by
dietary supplements is often found as
iron (II) fumarate, although iron sulfate is cheaper and is absorbed equally well. Elemental iron, despite being absorbed to a much smaller extent (stomach acid is sufficient to convert some of it to ferrous iron), is often added to foods such as breakfast cereals or "enriched" wheat flour (where it is listed as "reduced iron" in the list of ingredients). Iron is most available to the body when chelated to amino acids - iron in this form is ten to fifteen times more bioavailable than any other, 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.
[ ''Conversations on Chelation and Mineral Nutrition'', , H. DeWayne, Ashmead, Keats Publishing, 1989, ISBN 0-87983-501-X ] The
RDA for iron varies considerably based on age, gender, and source of dietary iron (
heme-based iron has higher
bioavailability)
[12]. Infants will require iron supplements if they are not breast-fed.
Blood donors are at special risk of low iron levels and are often advised to supplement their iron intake.
Regulation of iron uptake
Excessive iron can be toxic, because free ferrous iron reacts 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.
Iron uptake is tightly regulated by the human body, which has no physiological means of excreting iron, so controls iron levels solely by regulating uptake. Although uptake is regulated, large amounts of ingested iron can cause excessive levels of iron in the blood, because high iron levels can cause damage to the cells of the
gastrointestinal tract that prevents them from regulating iron absorption. High blood concentrations of iron damage cells in the
heart,
liver and elsewhere, which can cause serious problems, including long-term organ damage and even death.
Humans experience iron toxicity above 20 milligrams of iron for every
kilogram of mass, and 60 milligrams per kilogram is a
lethal dose.
[13] Over-consumption 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 cause of death in children under six
. The
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.
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 should 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.
[14]
The medical management of iron toxicity is complex, and can include use of a specific
chelating agent called deferoxamine to bind and expel excess iron from the body.
Bibliography
★
Los Alamos National Laboratory — Iron
★ 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.
★ http://www.webelements.com/webelements/elements/text/Fe/xtal.html
References
1. The Little Plankton That Could…Maybe, Vivian Marx, , , Scientific American, 2002
2. The Effect of Iron on Plankton Use of CO2
3. The Iron Hypothesis
4. Researchers 'seed' ocean with iron to soak up CO2 Steve O'Conner
5. Dauphas, N. & Rouxel, O. 2006. Mass spectrometry and natural variations of iron isotopes. ''Mass Spectrometry Reviews'', '25,' 515-550
6. Fox, B. A.; Threlfall, T. L. ''Organic Syntheses'', Coll. Vol. 5, p.346 (1973); Vol. 44, p.34 (1964). (Article)
7. Blomquist, A. T.; Dinguid, L. I. ''J. Org. Chem.'' '1947', ''12'', 718 & 723.
8. Clarke, H. T.; Dreger, E. E. ''Org. Syn.'', Coll. Vol. 1, p.304 (1941); Vol. 6, p.52 (1926). (Article)
9. den Hertog, J.; Overhoff, J. ''Recl. Trav. Chim. Pays-Bas'' '1950', ''69'', 468.
10. How Mammals Acquire and Distribute Iron Needed for Oxygen-Based Metabolism Tracey A. Rouault
11. http://www.eatwell.gov.uk/healthissues/irondeficiency/
12. Dietary Reference Intakes: Elements
13.
Toxicity, Iron
14. Durupt S, Durieu I, Nove-Josserand R, et al: [Hereditary hemochromatosis]. Rev Med Interne 2000 Nov; 21(11): 961-71[Medline].
16. Doulias PT, Christoforidis S, Brunk UT, Galaris D. Endosomal and lysosomal effects of desferrioxamine: protection of HeLa cells from hydrogen peroxide-induced DNA damage and induction of cell-cycle arrest. Free Radic Biol Med. 2003;35:719-28.
See also
★
El Mutún in
Bolivia, where 20% of the world's accessible iron and
magnesium is located
★
Iron (metaphor)
★
Iron Age
★
Iron fertilization - Fertilization of oceans to stimulate
phytoplankton growth
★
Pelletizing - Process of creation of iron ore pellets
★
Al-Hadid (Iron) in the
Qur'an
★
Specht Building - A historic landmark in
Omaha, Nebraska utilizing an iron facade.
External links
★
WebElements.com – Iron
★
It's Elemental – Iron
★
The Most Tightly Bound Nuclei