84-780: Thabazimbi is an iron mining town in the Limpopo province of South Africa . The town is at the feet of the Ysterberg and is surrounded by the Witfonteinrand and Boshofberg with the majestic Kransberg in the background. The name Thabazimbi means mountain of iron because of the large iron ore reef that was discovered in 1919 by J. H. Williams. The mine boasts one of the largest mining shafts in Africa. More than two million tonnes of ore are mined every year and hauled by train to Mittal 's iron and steel works. The railway line from Rustenburg reached
168-434: A body-centered cubic (bcc) crystal structure . As it cools further to 1394 °C, it changes to its γ-iron allotrope, a face-centered cubic (fcc) crystal structure, or austenite . At 912 °C and below, the crystal structure again becomes the bcc α-iron allotrope. The physical properties of iron at very high pressures and temperatures have also been studied extensively, because of their relevance to theories about
252-430: A nuclear spin (− 1 ⁄ 2 ). The nuclide Fe theoretically can undergo double electron capture to Cr, but the process has never been observed and only a lower limit on the half-life of 4.4×10 years has been established. Fe is an extinct radionuclide of long half-life (2.6 million years). It is not found on Earth, but its ultimate decay product is its granddaughter, the stable nuclide Ni . Much of
336-499: A supernova for their formation, involving rapid neutron capture by starting Fe nuclei. In the far future of the universe, assuming that proton decay does not occur, cold fusion occurring via quantum tunnelling would cause the light nuclei in ordinary matter to fuse into Fe nuclei. Fission and alpha-particle emission would then make heavy nuclei decay into iron, converting all stellar-mass objects to cold spheres of pure iron. Iron's abundance in rocky planets like Earth
420-437: A deep violet complex: Passivation (chemistry) In physical chemistry and engineering, passivation is coating a material so that it becomes "passive", that is, less readily affected or corroded by the environment. Passivation involves creation of an outer layer of shield material that is applied as a microcoating, created by chemical reaction with the base material, or allowed to build by spontaneous oxidation in
504-565: A dilute solution of nitric acid and peroxide alternating with deionized water . The nitric acid and peroxide mixture oxidizes and dissolves any impurities on the inner surface of the container, and the deionized water rinses away the acid and oxidized impurities. Generally, there are two main ways to passivate aluminium alloys (not counting plating , painting , and other barrier coatings): chromate conversion coating and anodizing . Alclading , which metallurgically bonds thin layers of pure aluminium or alloy to different base aluminium alloy,
588-454: A distorted sodium chloride structure. The binary ferrous and ferric halides are well-known. The ferrous halides typically arise from treating iron metal with the corresponding hydrohalic acid to give the corresponding hydrated salts. Iron reacts with fluorine, chlorine, and bromine to give the corresponding ferric halides, ferric chloride being the most common. Ferric iodide is an exception, being thermodynamically unstable due to
672-411: A gel-like composition hydrated with water. Chromate conversion is a common way of passivating not only aluminium, but also zinc , cadmium , copper , silver , magnesium , and tin alloys. Anodizing is an electrolytic process that forms a thicker oxide layer. The anodic coating consists of hydrated aluminium oxide and is considered resistant to corrosion and abrasion. This finish is more robust than
756-399: A hard, relatively inert surface layer, usually an oxide (termed the "native oxide layer") or a nitride , that serves as a passivation layer - i.e. these metals are "self-protecting". In the case of silver , the dark tarnish is a passivation layer of silver sulfide formed from reaction with environmental hydrogen sulfide . Aluminium similarly forms a stable protective oxide layer which
840-553: A macroscopic piece of iron will have a nearly zero overall magnetic field. Application of an external magnetic field causes the domains that are magnetized in the same general direction to grow at the expense of adjacent ones that point in other directions, reinforcing the external field. This effect is exploited in devices that need to channel magnetic fields to fulfill design function, such as electrical transformers , magnetic recording heads, and electric motors . Impurities, lattice defects , or grain and particle boundaries can "pin"
924-475: A mixture of O 2 /Ar. Iron(IV) is a common intermediate in many biochemical oxidation reactions. Numerous organoiron 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 . Many mixed valence compounds contain both iron(II) and iron(III) centers, such as magnetite and Prussian blue ( Fe 4 (Fe[CN] 6 ) 3 ). The latter
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#17328550986911008-447: A piece of iron is placed in dilute nitric acid , it will dissolve and produce hydrogen , but if the iron is placed in concentrated nitric acid and then returned to the dilute nitric acid, little or no reaction will take place. In 1836, Schönbein named the first state the active condition and the second the passive condition while Faraday proposed the modern explanation of the oxide film described above (Schönbein disagreed with it), which
1092-442: A process called oxidation , which creates a physical barrier to corrosion or further oxidation in many environments. Some aluminium alloys , however, do not form the oxide layer well, and thus are not protected against corrosion. There are methods to enhance the formation of the oxide layer for certain alloys. For example, prior to storing hydrogen peroxide in an aluminium container, the container can be passivated by rinsing it with
1176-471: A result, mercury is traded in standardized 76 pound flasks (34 kg) made of iron. Iron is by far the most reactive element in its group; it is pyrophoric when finely divided and dissolves easily in dilute acids, giving Fe . However, it does not react with concentrated nitric acid and other oxidizing acids due to the formation of an impervious oxide layer, which can nevertheless react with hydrochloric acid . High-purity iron, called electrolytic iron ,
1260-402: A thickness of about 1.5 nm for silicon, 1–10 nm for beryllium , and 1 nm initially for titanium , growing to 25 nm after several years. Similarly, for aluminium, it grows to about 5 nm after several years. In the context of the semiconductor device fabrication , such as silicon MOSFET transistors and solar cells , surface passivation refers not only to reducing
1344-470: A thin passivation layer of titanium oxide , mostly titanium dioxide . This layer makes it resistant to further corrosion, aside from gradual growth of the oxide layer, thickening to ~25 nm after several years in air. This protective layer makes it suitable for use even in corrosive environments such as sea water. Titanium can be anodized to produce a thicker passivation layer. As with many other metals, this layer causes thin-film interference which makes
1428-455: A type of rock consisting of repeated thin layers of iron oxides alternating with bands of iron-poor shale and chert . The banded iron formations were laid down in the time between 3,700 million years ago and 1,800 million years ago . Materials containing finely ground iron(III) oxides or oxide-hydroxides, such as ochre , have been used as yellow, red, and brown pigments since pre-historical times. They contribute as well to
1512-435: A very large coordination and organometallic chemistry : indeed, it was the discovery of an iron compound, ferrocene , that revolutionalized the latter field in the 1950s. Iron is sometimes considered as a prototype for the entire block of transition metals, due to its abundance and the immense role it has played in the technological progress of humanity. Its 26 electrons are arranged in the configuration [Ar]3d 4s , of which
1596-814: Is a chemical element ; it has the symbol Fe (from Latin ferrum 'iron') and atomic number 26. It is a metal that belongs to the first transition series and group 8 of the periodic table . It is, by mass, the most common element on Earth , forming much of Earth's outer and inner core . It is the fourth most abundant element in the Earth's crust , being mainly deposited by meteorites in its metallic state. Extracting usable metal from iron ores requires kilns or furnaces capable of reaching 1,500 °C (2,730 °F), about 500 °C (932 °F) higher than that required to smelt copper . Humans started to master that process in Eurasia during
1680-630: Is also rarely found in basalts that have formed from magmas that have come into contact with carbon-rich sedimentary rocks, which have reduced the oxygen fugacity sufficiently for iron to crystallize. This is known as telluric iron and is described from a few localities, such as Disko Island in West Greenland, Yakutia in Russia and Bühl in Germany. Ferropericlase (Mg,Fe)O , a solid solution of periclase (MgO) and wüstite (FeO), makes up about 20% of
1764-683: Is also the home of some of the Tuli elephants that were caught up in controversy in 1999 involving animal cruelty in South Africa. In the post-apartheid era, the town made headlines in 2003 as the site of Kamp Staaldraad , the Springboks' infamous training camp prior to the Rugby World Cup . The excesses of Kamp Staaldraad helped lead to an almost complete housecleaning of the upper administrative levels of South African rugby union . Iron Iron
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#17328550986911848-491: Is commonly used as a passivating acid for stainless steel, citric acid is gaining in popularity as it is far less dangerous to handle, less toxic, and biodegradable, making disposal less of a challenge. Passivating temperatures can range from ambient to 60 °C (140 °F), while minimum passivation times are usually 20 to 30 minutes. After passivation, the parts are neutralized using a bath of aqueous sodium hydroxide , then rinsed with clean water and dried. The passive surface
1932-407: Is considered to be resistant to rust, due to its oxide layer. Iron forms various oxide and hydroxide compounds ; the most common are iron(II,III) oxide (Fe 3 O 4 ), and iron(III) oxide (Fe 2 O 3 ). Iron(II) oxide also exists, though it is unstable at room temperature. Despite their names, they are actually all non-stoichiometric compounds whose compositions may vary. These oxides are
2016-495: Is due to its abundant production during the runaway fusion and explosion of type Ia supernovae , which scatters the iron into space. Metallic or native iron is rarely found on the surface of the Earth because it tends to oxidize. However, both the Earth's inner and outer core , which together account for 35% of the mass of the whole Earth, are believed to consist largely of an iron alloy, possibly with nickel . Electric currents in
2100-474: Is experimentally well defined for pressures less than 50 GPa. For greater pressures, published data (as of 2007) still varies by tens of gigapascals and over a thousand kelvin. Below its Curie point of 770 °C (1,420 °F; 1,040 K), α-iron changes from paramagnetic to ferromagnetic : the spins of the two unpaired electrons in each atom generally align with the spins of its neighbors, creating an overall magnetic field . This happens because
2184-443: Is in Earth's crust only amounts to about 5% of the overall mass of the crust and is thus only the fourth most abundant element in that layer (after oxygen , silicon , and aluminium ). Most of the iron in the crust is combined with various other elements to form many iron minerals . An important class is the iron oxide minerals such as hematite (Fe 2 O 3 ), magnetite (Fe 3 O 4 ), and siderite (FeCO 3 ), which are
2268-401: Is not like that of Mn with its weak, spin-forbidden d–d bands, because Fe has higher positive charge and is more polarizing, lowering the energy of its ligand-to-metal charge transfer absorptions. Thus, all the above complexes are rather strongly colored, with the single exception of the hexaquo ion – and even that has a spectrum dominated by charge transfer in the near ultraviolet region. On
2352-409: Is not strictly passivation of the base alloy. However, the aluminium layer clad on is designed to spontaneously develop the oxide layer and thus protect the base alloy. Chromate conversion coating converts the surface aluminium to an aluminium chromate coating in the range of 0.00001–0.00004 inches (250–1,000 nm) in thickness. Aluminium chromate conversion coatings are amorphous in structure with
2436-443: Is obtained. These molecules will generally have lone electron pairs or pi-electrons, so they can bind to the defective states on the surface of the cell film and thus achieve passivation of the material. Therefore, molecules such as carbonyl , nitrogen-containing molecules, and sulfur-containing molecules are considered, and recently it has been shown that π electrons can also play a role. In addition, passivation not only improves
2520-479: Is often required as an additive to oxidise the chromium in certain 'types' of nitric-based acid baths, however this chemical is highly toxic. With citric acid, simply rinsing and drying the part and allowing the air to oxidise it, or in some cases the application of other chemicals, is used to perform the passivation of the surface. It is not uncommon for some aerospace manufacturers to have additional guidelines and regulations when passivating their products that exceed
2604-407: Is possible, but nonetheless the sequence does effectively end at Ni because conditions in stellar interiors cause the competition between photodisintegration and the alpha process to favor photodisintegration around Ni. This Ni, which has a half-life of about 6 days, is created in quantity in these stars, but soon decays by two successive positron emissions within supernova decay products in
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2688-548: Is somewhat different). Pieces of magnetite with natural permanent magnetization ( lodestones ) provided the earliest compasses for navigation. Particles of magnetite were extensively used in magnetic recording media such as core memories , magnetic tapes , floppies , and disks , until they were replaced by cobalt -based materials. Iron has four stable isotopes : Fe (5.845% of natural iron), Fe (91.754%), Fe (2.119%) and Fe (0.282%). Twenty-four artificial isotopes have also been created. Of these stable isotopes, only Fe has
2772-442: Is such a strong oxidizing agent that it oxidizes ammonia to nitrogen (N 2 ) and water to oxygen: The pale-violet hex aquo complex [Fe(H 2 O) 6 ] is an acid such that above pH 0 it is fully hydrolyzed: As pH rises above 0 the above yellow hydrolyzed species form and as it rises above 2–3, reddish-brown hydrous iron(III) oxide precipitates out of solution. Although Fe has a d configuration, its absorption spectrum
2856-502: Is supposed to have an orthorhombic or a double hcp structure. (Confusingly, the term "β-iron" is sometimes also used to refer to α-iron above its Curie point, when it changes from being ferromagnetic to paramagnetic, even though its crystal structure has not changed. ) The inner core of the Earth is generally presumed to consist of an iron- nickel alloy with ε (or β) structure. The melting and boiling points of iron, along with its enthalpy of atomization , are lower than those of
2940-418: Is thus very important economically, and iron is the cheapest metal, with a price of a few dollars per kilogram or pound. Pristine and smooth pure iron surfaces are a mirror-like silvery-gray. Iron reacts readily with oxygen and water to produce brown-to-black hydrated iron oxides , commonly known as rust . Unlike the oxides of some other metals that form passivating layers, rust occupies more volume than
3024-451: Is used as the traditional "blue" in blueprints . Iron is the first of the transition metals that cannot reach its group oxidation state of +8, although its heavier congeners ruthenium and osmium can, with ruthenium having more difficulty than osmium. Ruthenium exhibits an aqueous cationic chemistry in its low oxidation states similar to that of iron, but osmium does not, favoring high oxidation states in which it forms anionic complexes. In
3108-437: Is used in chemical actinometry and along with its sodium salt undergoes photoreduction applied in old-style photographic processes. The dihydrate of iron(II) oxalate has a polymeric structure with co-planar oxalate ions bridging between iron centres with the water of crystallisation located forming the caps of each octahedron, as illustrated below. Iron(III) complexes are quite similar to those of chromium (III) with
3192-473: Is usually implemented by thermal oxidation at about 1000 °C to form a coating of silicon dioxide . Surface passivation is critical to solar cell efficiency . The effect of passivation on the efficiency of solar cells ranges from 3–7%. The surface resistivity is high, > 100 Ωcm. The easiest and most widely studied method to improve perovskite solar cells is passivation. These defects usually lead to deep energy level defects in solar cells due to
3276-408: Is validated using humidity, elevated temperature, a rusting agent (salt spray), or some combination of the three. The passivation process removes exogenous iron, creates/restores a passive oxide layer that prevents further oxidation ( rust ), and cleans the parts of dirt, scale, or other welding-generated compounds (e.g. oxides). Passivation processes are generally controlled by industry standards,
3360-451: Is when small spots on the surface begin to rust because grain boundaries or embedded bits of foreign matter (such as grinding swarf ) allow water molecules to oxidize some of the iron in those spots despite the alloying chromium . This is called rouging . Some grades of stainless steel are especially resistant to rouging; parts made from them may therefore forgo any passivation step, depending on engineering decisions. Common among all of
3444-539: Is why it does not "rust". (In contrast, some base metals, notably iron , oxidize readily to form a rough, porous coating of rust that adheres loosely, is of higher volume than the original displaced metal, and sloughs off readily; all of which permit & promote further oxidation.) The passivation layer of oxide markedly slows further oxidation and corrosion in room-temperature air for aluminium , beryllium , chromium , zinc , titanium , and silicon (a metalloid ). The inert surface layer formed by reaction with air has
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3528-557: The 2nd millennium BC and the use of iron tools and weapons began to displace copper alloys – in some regions, only around 1200 BC. That event is considered the transition from the Bronze Age to the Iron Age . In the modern world , iron alloys, such as steel , stainless steel , cast iron and special steels , are by far the most common industrial metals, due to their mechanical properties and low cost. The iron and steel industry
3612-432: The supernova remnant gas cloud, first to radioactive Co, and then to stable Fe. As such, 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 . It is also very common in the universe, relative to other stable metals of approximately the same atomic weight . Iron is the sixth most abundant element in
3696-488: The trans - chlorohydridobis(bis-1,2-(diphenylphosphino)ethane)iron(II) complex is used as a starting material for compounds with the Fe( dppe ) 2 moiety . The ferrioxalate ion with three oxalate ligands displays helical chirality with its two non-superposable geometries labelled Λ (lambda) for the left-handed screw axis and Δ (delta) for the right-handed screw axis, in line with IUPAC conventions. Potassium ferrioxalate
3780-466: The universe , and the most common refractory element. Although a further tiny energy gain could be extracted by synthesizing Ni , which has a marginally higher binding energy than Fe, conditions in stars are unsuitable for this process. Element production in supernovas greatly favor iron over nickel, and in any case, Fe still has a lower mass per nucleon than Ni due to its higher fraction of lighter protons. Hence, elements heavier than iron require
3864-570: The 3d and 4s electrons are relatively close in energy, and thus a number of electrons can be ionized. Iron forms compounds mainly in the oxidation states +2 ( iron(II) , "ferrous") and +3 ( iron(III) , "ferric"). Iron also occurs in higher oxidation states , e.g., the purple potassium ferrate (K 2 FeO 4 ), which contains iron in its +6 oxidation state. The anion [FeO 4 ] with iron in its +7 oxidation state, along with an iron(V)-peroxo isomer, has been detected by infrared spectroscopy at 4 K after cocondensation of laser-ablated Fe atoms with
3948-589: The Earth's surface. Items made of cold-worked meteoritic iron have been found in various archaeological sites dating from a time when iron smelting had not yet been developed; and the Inuit in Greenland have been reported to use iron from the Cape York meteorite for tools and hunting weapons. About 1 in 20 meteorites consist of the unique iron-nickel minerals taenite (35–80% iron) and kamacite (90–95% iron). Native iron
4032-555: The air. As a technique, passivation is the use of a light coat of a protective material, such as metal oxide , to create a shield against corrosion . Passivation of silicon is used during fabrication of microelectronic devices. Undesired passivation of electrodes, called "fouling", increases the circuit resistance so it interferes with some electrochemical applications such as electrocoagulation for wastewater treatment, amperometric chemical sensing , and electrochemical synthesis . When exposed to air, many metals naturally form
4116-441: The area in the 1930s and full scale iron and steel production began. The town was proclaimed in 1953. Kumba Iron Ore, previously Kumba Resources , is now the principal operator of the iron ore mine. The Marakele National Park about 20 km north-east of the town and in the heart of Waterberg Mountains is characterised by contrasting mountain landscapes, hills and valleys, as well a variety of wildlife. Marakele National Park
4200-450: The brown deposits present in a sizeable number of streams. Due to its electronic structure, iron has a very large coordination and organometallic chemistry. Many coordination compounds of iron are known. A typical six-coordinate anion is hexachloroferrate(III), [FeCl 6 ] , found in the mixed salt tetrakis(methylammonium) hexachloroferrate(III) chloride . Complexes with multiple bidentate ligands have geometric isomers . For example,
4284-484: The buildup of an electronic barrier opposing electron flow and an electronic depletion region that prevents further oxidation reactions. These results indicate a mechanism of "electronic passivation". The electronic properties of this semiconducting oxide film also provide a mechanistic explanation of corrosion mediated by chloride , which creates surface states at the oxide surface that lead to electronic breakthrough, restoration of anodic currents, and disruption of
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#17328550986914368-407: The chemical reactivity of the surface but also to eliminating the dangling bonds and other defects that form electronic surface states , which impair performance of the devices. Surface passivation of silicon usually consists of high-temperature thermal oxidation . There has been much interest in determining the mechanisms that govern the increase of thickness of the oxide layer over time. Some of
4452-683: The color of various rocks and clays , including entire geological formations like the Painted Hills in Oregon and the Buntsandstein ("colored sandstone", British Bunter ). Through Eisensandstein (a jurassic 'iron sandstone', e.g. from Donzdorf in Germany) and Bath stone in the UK, iron compounds are responsible for the yellowish color of many historical buildings and sculptures. The proverbial red color of
4536-464: The cores of the Earth and other planets. Above approximately 10 GPa and temperatures of a few hundred kelvin or less, α-iron changes into another 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. Some controversial experimental evidence exists for a stable β phase at pressures above 50 GPa and temperatures of at least 1500 K. It
4620-404: The different specifications and types are the following steps: Prior to passivation, the object must be cleaned of any contaminants and generally must undergo a validating test to prove that the surface is 'clean.' The object is then placed in an acidic passivating bath that meets the temperature and chemical requirements of the method and type specified between customer and vendor. While nitric acid
4704-401: The domains in the new positions, so that the effect persists even after the external field is removed – thus turning the iron object into a (permanent) magnet . Similar behavior is exhibited by some iron compounds, such as the ferrites including the mineral magnetite , a crystalline form of the mixed iron(II,III) oxide Fe 3 O 4 (although the atomic-scale mechanism, ferrimagnetism ,
4788-479: The earlier 3d elements from scandium to chromium , showing the lessened contribution of the 3d electrons to metallic bonding as they are attracted more and more into the inert core by the nucleus; however, they are higher than the values for the previous element manganese because that element has a half-filled 3d sub-shell and consequently its d-electrons are not easily delocalized. This same trend appears for ruthenium but not osmium . The melting point of iron
4872-433: The electronic passivation mechanism ("transpassivation"). The fact that iron doesn't react with concentrated nitric acid was discovered by Mikhail Lomonosov in 1738 and rediscovered by James Keir in 1790, who also noted that such pre-immersed Fe doesn't reduce silver from nitrate anymore. In the 1830s, Michael Faraday and Christian Friedrich Schönbein studied that issue systematically and demonstrated that when
4956-406: The exception of iron(III)'s preference for O -donor instead of N -donor ligands. The latter tend to be rather more unstable than iron(II) complexes and often dissociate in water. Many Fe–O complexes show intense colors and are used as tests for phenols or enols . For example, in the ferric chloride test , used to determine the presence of phenols, iron(III) chloride reacts with a phenol to form
5040-417: The formation of a passivation layer on the surface of the metals to which they are applied. Some compounds, dissolved in solutions ( chromates , molybdates ) form non-reactive and low solubility films on metal surfaces. It has been shown using electrochemical scanning tunneling microscopy that during iron passivation, an n-type semiconductor Fe(III) oxide grows at the interface with the metal that leads to
5124-462: The global stock of iron in use in society is 2,200 kg per capita. More-developed countries differ in this respect from less-developed countries (7,000–14,000 vs 2,000 kg per capita). Ocean science demonstrated the role of the iron in the ancient seas in both marine biota and climate. Iron shows the characteristic chemical properties of the transition metals , namely the ability to form variable oxidation states differing by steps of one and
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#17328550986915208-640: The important factors are the volume of oxide relative to the volume of the parent metal, the mechanism of oxygen diffusion through the metal oxide to the parent metal, and the relative chemical potential of the oxide. Boundaries between micro grains, if the oxide layer is crystalline, form an important pathway for oxygen to reach the unoxidized metal below. For this reason, vitreous oxide coatings – which lack grain boundaries – can retard oxidation. The conditions necessary, but not sufficient, for passivation are recorded in Pourbaix diagrams . Some corrosion inhibitors help
5292-449: The liquid outer core are believed to be the origin of the Earth's magnetic field . The other terrestrial planets ( Mercury , Venus , and Mars ) as well as the Moon are believed to have a metallic core consisting mostly of iron. The M-type asteroids are also believed to be partly or mostly made of metallic iron alloy. The rare iron meteorites are the main form of natural metallic iron on
5376-446: The literature, this mineral phase of the lower mantle is also often called magnesiowüstite. Silicate perovskite may form up to 93% of the lower mantle, and the magnesium iron form, (Mg,Fe)SiO 3 , is considered to be the most abundant mineral in the Earth, making up 38% of its volume. While iron is the most abundant element on Earth, most of this iron is concentrated in the inner and outer cores. The fraction of iron that
5460-407: The major ores of iron . Many igneous rocks also contain the sulfide minerals pyrrhotite and pentlandite . During weathering , iron tends to leach from sulfide deposits as the sulfate and from silicate deposits as the bicarbonate. Both of these are oxidized in aqueous solution and precipitate in even mildly elevated pH as iron(III) oxide . Large deposits of iron are banded iron formations ,
5544-775: The metal and thus flakes off, exposing more fresh surfaces for corrosion. Chemically, the most common oxidation states of iron are iron(II) and iron(III) . Iron shares many properties of other transition metals, including the other group 8 elements , ruthenium and osmium . Iron forms compounds in a wide range of oxidation states , −4 to +7. Iron also forms many coordination compounds ; some of them, such as ferrocene , ferrioxalate , and Prussian blue have substantial industrial, medical, or research applications. The body of an adult human contains about 4 grams (0.005% body weight) of iron, mostly in hemoglobin and myoglobin . These two proteins play essential roles in oxygen transport by blood and oxygen storage in muscles . To maintain
5628-410: The metal surface appear colored, with the thickness of the passivation layer directly affecting the color produced. Nickel can be used for handling elemental fluorine , owing to the formation of a passivation layer of nickel fluoride . This fact is useful in water treatment and sewage treatment applications. In the area of microelectronics and photovoltaic solar cells , surface passivation
5712-606: The meteorites Semarkona and Chervony Kut, a correlation between the concentration of Ni, the granddaughter of Fe, and the abundance of the stable iron isotopes provided evidence for the existence of Fe at the time of formation of the Solar System . Possibly the energy released by the decay of Fe, along with that released by Al , contributed to the remelting and differentiation of asteroids after their formation 4.6 billion years ago. The abundance of Ni present in extraterrestrial material may bring further insight into
5796-515: The most prevalent among them today being ASTM A 967 and AMS 2700. These industry standards generally list several passivation processes that can be used, with the choice of specific method left to the customer and vendor. The "method" is either a nitric acid -based passivating bath, or a citric acid -based bath, these acids remove surface iron and rust, while sparing the chromium. The various 'types' listed under each method refer to differences in acid bath temperature and concentration. Sodium dichromate
5880-574: The national standard. Often, these requirements will be cascaded down using Nadcap or some other accreditation system. Various testing methods are available to determine the passivation (or passive state) of stainless steel. The most common methods for validating the passivity of a part is some combination of high humidity and heat for a period of time, intended to induce rusting. Electro-chemical testers can also be utilized to commercially verify passivation. The surface of titanium and of titanium-rich alloys oxidizes immediately upon exposure to air to form
5964-559: The necessary levels, human iron metabolism requires a minimum of iron in the diet. Iron is also the metal at the active site of many important redox enzymes dealing with cellular respiration and oxidation and reduction in plants and animals. At least four allotropes of iron (differing atom arrangements in the solid) are known, conventionally denoted α , γ , δ , and ε . The first three forms are observed at ordinary pressures. As molten iron cools past its freezing point of 1538 °C, it crystallizes into its δ allotrope, which has
6048-436: The orbitals of those two electrons (d z and d x − y ) do not point toward neighboring atoms in the lattice, and therefore are not involved in metallic bonding. In the absence of an external source of magnetic field, the atoms get spontaneously partitioned into magnetic domains , about 10 micrometers across, such that the atoms in each domain have parallel spins, but some domains have other orientations. Thus
6132-533: The origin and early history of the Solar System . The most abundant iron isotope Fe is of particular interest to nuclear scientists because it represents the most common endpoint of nucleosynthesis . Since Ni (14 alpha particles ) is easily produced from lighter nuclei in the alpha process in nuclear reactions in supernovae (see silicon burning process ), it is the endpoint of fusion chains inside extremely massive stars . Although adding more alpha particles
6216-444: The other hand, the pale green iron(II) hexaquo ion [Fe(H 2 O) 6 ] does not undergo appreciable hydrolysis. Carbon dioxide is not evolved when carbonate anions are added, which instead results in white iron(II) carbonate being precipitated out. In excess carbon dioxide this forms the slightly soluble bicarbonate, which occurs commonly in groundwater, but it oxidises quickly in air to form iron(III) oxide that accounts for
6300-483: The other processes and also provides electrical insulation , which the other two processes may not. In carbon quantum dot (CQD) technology, CQDs are small carbon nanoparticles (less than 10 nm in size) with some form of surface passivation. Ferrous materials, including steel, may be somewhat protected by promoting oxidation ("rust") and then converting the oxidation to a metalophosphate by using phosphoric acid and add further protection by surface coating. As
6384-581: The oxidizing power of Fe and the high reducing power of I : Ferric iodide, a black solid, is not stable in ordinary conditions, but can be prepared through the reaction of iron pentacarbonyl with iodine and carbon monoxide in the presence of hexane and light at the temperature of −20 °C, with oxygen and water excluded. Complexes of ferric iodide with some soft bases are known to be stable compounds. The standard reduction potentials in acidic aqueous solution for some common iron ions are given below: The red-purple tetrahedral ferrate (VI) anion
6468-497: The past work on isotopic composition of iron has focused on the nucleosynthesis of Fe through studies of meteorites and ore formation. In the last decade, advances in mass spectrometry have allowed the detection and quantification of minute, naturally occurring variations in the ratios of the stable isotopes of iron. Much of this work is driven by the Earth and planetary science communities, although applications to biological and industrial systems are emerging. In phases of
6552-412: The presence of hanging bonds on the surface of perovskite films. Usually, small molecules or polymers are doped to interact with the hanging bonds and thus reduce the defect states. This process is similar to Tetris, i.e., we always want the layer to be full. A small molecule with the function of passivation is some kind of square that can be inserted where there is an empty space and then a complete layer
6636-414: 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 (FeS 2 ), also known as fool's gold owing to its golden luster. It is not an iron(IV) compound, but is actually an iron(II) polysulfide containing Fe and S 2 ions in
6720-437: The second half of the 3d transition series, vertical similarities down the groups compete with the horizontal similarities of iron with its neighbors cobalt and nickel in the periodic table, which are also ferromagnetic at room temperature and share similar chemistry. As such, iron, cobalt, and nickel are sometimes grouped together as the iron triad . Unlike many other metals, iron does not form amalgams with mercury . As
6804-547: The surface of Mars is derived from an iron oxide-rich regolith . Significant amounts of iron occur in the iron sulfide mineral pyrite (FeS 2 ), but it is difficult to extract iron from it and it is therefore not exploited. In fact, iron is so common that production generally focuses only on ores with very high quantities of it. According to the International Resource Panel 's Metal Stocks in Society report ,
6888-591: The uncoated surface is water-soluble, a preferred method is to form manganese or zinc compounds by a process commonly known as parkerizing or phosphate conversion . Older, less effective but chemically similar electrochemical conversion coatings included black oxidizing , historically known as bluing or browning . Ordinary steel forms a passivating layer in alkali environments, as reinforcing bar does in concrete . Stainless steels are corrosion-resistant, but they are not completely impervious to rusting. One common mode of corrosion in corrosion-resistant steels
6972-455: The volume of the lower mantle of the Earth, which makes it the second most abundant mineral phase in that region after silicate perovskite (Mg,Fe)SiO 3 ; it also is the major host for iron in the lower mantle. At the bottom of the transition zone of the mantle, the reaction γ- (Mg,Fe) 2 [SiO 4 ] ↔ (Mg,Fe)[SiO 3 ] + (Mg,Fe)O transforms γ-olivine into a mixture of silicate perovskite and ferropericlase and vice versa. In
7056-401: Was experimentally proven by Ulick Richardson Evans only in 1927. Between 1955 and 1957, Carl Frosch and Lincoln Derrick discovered surface passivation of silicon wafers by silicon dioxide, using passivation to build the first silicon dioxide field effect transistors. Aluminium naturally forms a thin surface layer of aluminium oxide on contact with oxygen in the atmosphere through
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