Chromium is a chemical element with symbol Cr and atomic number 24. It is the first element in group 6. It is a steely-grey, lustrous, hard and brittle transition metal. Chromium boasts a high usage rate as a metal that is able to be highly polished while resisting tarnishing. Chromium is also the main additive in stainless steel, a popular steel alloy due to its uncommonly high specular reflection. Simple polished chromium reflects almost 70% of the visible spectrum, with almost 90% of infrared light being reflected. The name of the element is derived from the Greek word χρῶμα, chrōma, meaning color, because many chromium compounds are intensely colored.
Ferrochromium alloy is commercially produced from chromite by silicothermic or aluminothermic reactions and chromium metal by roasting and leaching processes followed by reduction with carbon and then aluminium. Chromium metal is of high value for its high corrosion resistance and hardness. A major development in steel production was the discovery that steel could be made highly resistant to corrosion and discoloration by adding metallic chromium to form stainless steel. Stainless steel and chrome plating (electroplating with chromium) together comprise 85% of the commercial use.
In the United States, trivalent chromium (Cr(III)) ion is considered an essential nutrient in humans for insulin, sugar and lipid metabolism. However, in 2014, the European Food Safety Authority, acting for the European Union, concluded that there was not sufficient evidence for chromium to be recognized as essential.
|Standard atomic weight Ar, std(Cr)||51.9961(6)|
|Chromium in the periodic table|
|Atomic number (Z)||24|
|Element category||transition metal|
|Electron configuration||[Ar] 3d5 4s1|
Electrons per shell
|2, 8, 13, 1|
|Phase at STP||solid|
|Melting point||2180 K (1907 °C, 3465 °F)|
|Boiling point||2944 K (2671 °C, 4840 °F)|
|Density (near r.t.)||7.19 g/cm3|
|when liquid (at m.p.)||6.3 g/cm3|
|Heat of fusion||21.0 kJ/mol|
|Heat of vaporization||347 kJ/mol|
|Molar heat capacity||23.35 J/(mol·K)|
|Oxidation states||−4, −2, −1, +1, +2, +3, +4, +5, +6 (depending on the oxidation state, an acidic, basic, or amphoteric oxide)|
|Electronegativity||Pauling scale: 1.66|
|Atomic radius||empirical: 128 pm|
|Covalent radius||139±5 pm|
Spectral lines of chromium
|Crystal structure|| body-centered cubic (bcc)|
|Speed of sound thin rod||5940 m/s (at 20 °C)|
|Thermal expansion||4.9 µm/(m·K) (at 25 °C)|
|Thermal conductivity||93.9 W/(m·K)|
|Electrical resistivity||125 nΩ·m (at 20 °C)|
|Magnetic ordering||antiferromagnetic (rather: SDW)|
|Magnetic susceptibility||+280.0·10−6 cm3/mol (273 K)|
|Young's modulus||279 GPa|
|Shear modulus||115 GPa|
|Bulk modulus||160 GPa|
|Vickers hardness||1060 MPa|
|Brinell hardness||687–6500 MPa|
|Discovery and first isolation||Louis Nicolas Vauquelin (1794, 1797)|
|Main isotopes of chromium|
Chromium is the fourth transition metal found on the periodic table, and has an electron configuration of [Ar] 3d5 4s1. It is also the first element in the periodic table whose ground-state electron configuration violates the Aufbau principle. This occurs again later in the periodic table with other elements and their electron configurations, such as copper, niobium, and molybdenum. This occurs because electrons in the same orbital repel each other due to their like charges. In the previous elements, the energetic cost of promoting an electron to the next higher energy level is too great to compensate for that released by lessening inter-electronic repulsion. However, in the 3d transition metals, the energy gap between the 3d and the next-higher 4s subshell is very small, and because the 3d subshell is more compact than the 4s subshell, inter-electron repulsion is smaller between 4s electrons than between 3d electrons. This lowers the energetic cost of promotion and increases the energy released by it, so that the promotion becomes energetically feasible and one or even two electrons are always promoted to the 4s subshell. (Similar promotions happen for every transition metal atom but one, palladium.)
Chromium is the first element in the 3d series where the 3d electrons start to sink into the inert core; they thus contribute less to metallic bonding, and hence the melting and boiling points and the enthalpy of atomisation of chromium are lower than those of the preceding element vanadium. Chromium(VI) is a strong oxidising agent in contrast to the molybdenum(VI) and tungsten(VI) oxides.
Chromium is extremely hard, and is the third hardest element behind carbon (diamond) and boron. Its Mohs hardness is 8.5, which means that it can scratch samples of quartz and topaz, but can be scratched by corundum. Chromium is highly resistant to tarnishing, which makes it useful as a metal that preserves its outermost layer from corroding, unlike other metals such as copper, magnesium, and aluminium.
Chromium has a melting point of 1907 °C (3465 °F), which is relatively low compared to the majority of transition metals. However, it still has the second highest melting point out of all the Period 4 elements, being topped by vanadium by 3 °C (5 °F) at 1910 °C (3470 °F). The boiling point of 2671 °C (4840 °F), however, is comparatively lower, having the third lowest boiling point out of the Period 4 transition metals alone[a] behind manganese and zinc. The electrical resistivity of lead at 20 °C is 125 nanoohm-meters.
Chromium has an unusually high specular reflection in comparison to that of other transition metals. At 425 μm, chromium was found to have a relative maximum reflection of about 72% reflectance, before entering a depression in reflectivity, reaching a minimum of 62% reflectance at 750 μm before rising again to reflecting roughly 90% of 4000 μm of infrared waves.. When chromium is formed into a stainless steel alloy and polished, the specular reflection decreases with the inclusion of additional metals, yet is still rather high in comparison with other alloys. Between 40% and 60% of the visible spectrum is reflected from polished stainless steel. The explanation on why chromium displays such a high turnout of reflected photon waves in general, especially the 90% of infrared waves that were reflected, can be attributed to chromium's magnetic properties. Chromium has unique magnetic properties in the sense that chromium is the only elemental solid which shows antiferromagnetic ordering at room temperature (and below). Above 38 °C, its magnetic ordering changes to paramagnetic.. The antiferromagnetic properties, which cause the chromium atoms to temporarily ionize and bond with themselves, are present because the body-centric cubic's magnetic properties are disproportionate to the lattice periodicity. This is due to the fact that the magnetic moments at the cube's corners and the cube centers are not equal, but are still antiparallel. From here, the frequency-dependent relative permittivity of chromium, deriving from Maxwell's equations in conjunction with chromium's antiferromagnetivity, leaves chromium with a high infrared and visible light reflectance.
Chromium metal left standing in air is passivated by oxidation, forming a thin, protective, surface layer. This layer is a spinel structure only a few molecules thick. It is very dense, and prevents the diffusion of oxygen into the underlying metal. This is different from the spongy oxide that forms on iron and carbon steel, through which elemental oxygen continues to migrate, reaching the underlying material to cause continued further rusting. Passivation can be enhanced by short contact with oxidizing acids like nitric acid. Passivated chromium is stable against acids. Passivation can be removed with a strong reducing agent that destroys the protective oxide layer on the metal. Chromium metal treated in this way readily dissolves in weak acids.
Chromium, unlike such metals as iron and nickel, does not suffer from hydrogen embrittlement. However, it does suffer from nitrogen embrittlement, reacting with nitrogen from air and forming brittle nitrides at the high temperatures necessary to work the metal parts.
Naturally occurring chromium is composed of three stable isotopes; 52Cr, 53Cr and 54Cr, with 52Cr being the most abundant (83.789% natural abundance). 19 radioisotopes have been characterized, with the most stable being 50Cr with a half-life of (more than) 1.8×1017 years, and 51Cr with a half-life of 27.7 days. All of the remaining radioactive isotopes have half-lives that are less than 24 hours and the majority less than 1 minute. Chromium also has two metastable nuclear isomers.
53Cr is the radiogenic decay product of 53Mn (half-life = 3.74 million years). Chromium isotopes are typically collocated (and compounded) with manganese isotopes. This circumstance is useful in isotope geology. Manganese-chromium isotope ratios reinforce the evidence from 26Al and 107Pd concerning the early history of the solar system. Variations in 53Cr/52Cr and Mn/Cr ratios from several meteorites indicate an initial 53Mn/55Mn ratio that suggests Mn-Cr isotopic composition must result from in-situ decay of 53Mn in differentiated planetary bodies. Hence 53Cr provides additional evidence for nucleosynthetic processes immediately before coalescence of the solar system.
The isotopes of chromium range in atomic mass from 43 u (43Cr) to 67 u (67Cr). The primary decay mode before the most abundant stable isotope, 52Cr, is electron capture and the primary mode after is beta decay. 53Cr has been posited as a proxy for atmospheric oxygen concentration.
Chromium is a member of group 6, of the transition metals. Chromium(0) has an electron configuration of [Ar]3d54s1, owing to the lower energy of the high spin configuration. Chromium exhibits a wide range of oxidation states, but chromium being ionized into a cation with a positive 3 charge serves as chromium's most stable ionic state. The +3 and +6 states occur the most commonly within chromium compounds; charges of +1, +4 and +5 for chromium are rare, but do nevertheless occasionally exist.
A large number of chromium(III) compounds are known, such as chromium(III) nitrate, chromium(III) acetate, and chromium(III) oxide. Chromium(III) can be obtained by dissolving elemental chromium in acids like hydrochloric acid or sulfuric acid, but it can also be formed through the reduction of chromium(VI) by cytochrome c7. The Cr3+
ion has a similar radius (63 pm) to Al3+
(radius 50 pm), and they can replace each other in some compounds, such as in chrome alum and alum. When a trace amount of Cr3+
in corundum (aluminium oxide, Al2O3), pink sapphire or red-colored ruby is formed, depending on the amount of chromium.
Chromium(III) tends to form octahedral complexes. Commercially available chromium(III) chloride hydrate is the dark green complex [CrCl2(H2O)4]Cl. Closely related compounds are the pale green [CrCl(H2O)5]Cl2 and violet [Cr(H2O)6]Cl3. If water-free green chromium(III) chloride is dissolved in water, the green solution turns violet after some time as the chloride in the inner coordination sphere is replaced by water. This kind of reaction is also observed with solutions of chrome alum and other water-soluble chromium(III) salts.
Chromium(III) hydroxide (Cr(OH)3) is amphoteric, dissolving in acidic solutions to form [Cr(H2O)6]3+, and in basic solutions to form [Cr(OH)
. It is dehydrated by heating to form the green chromium(III) oxide (Cr2O3), a stable oxide with a crystal structure identical to that of corundum.
Chromium(VI) compounds are oxidants at low or neutral pH. Chromate anions (CrO2−
4) and dichromate (Cr2O72−) anions are the principal ions at this oxidation state. They exist at an equilibrium, determined by pH:
Sodium chromate is produced industrially by the oxidative roasting of chromite ore with calcium or sodium carbonate. The change in equilibrium is visible by a change from yellow (chromate) to orange (dichromate), such as when an acid is added to a neutral solution of potassium chromate. At yet lower pH values, further condensation to more complex oxyanions of chromium is possible.
They are, however, only moderately oxidizing at high pH:
Chromium(VI) compounds in solution can be detected by adding an acidic hydrogen peroxide solution. The unstable dark blue chromium(VI) peroxide (CrO5) is formed, which can be stabilized as an ether adduct CrO
Chromic acid has the hypothetical formula H
4. It is a vaguely described chemical, despite many well-defined chromates and dichromates being known. The dark red chromium(VI) oxide CrO
3, the acid anhydride of chromic acid, is sold industrially as "chromic acid". It can be produced by mixing sulfuric acid with dichromate, and is a strong oxidizing agent.
The oxidation state +5 is only realized in few compounds but are intermediates in many reactions involving oxidations by chromate. The only binary compound is the volatile chromium(V) fluoride (CrF5). This red solid has a melting point of 30 °C and a boiling point of 117 °C. It can be prepared by treating chromium metal with fluorine at 400 °C and 200 bar pressure. The peroxochromate(V) is another example of the +5 oxidation state. Potassium peroxochromate (K3[Cr(O2)4]) is made by reacting potassium chromate with hydrogen peroxide at low temperatures. This red brown compound is stable at room temperature but decomposes spontaneously at 150–170 °C.
Compounds of chromium(IV) (in the +4 oxidation state) are slightly more common than those of chromium(V). The tetrahalides, CrF4, CrCl4, and CrBr4, can be produced by treating the trihalides (CrX
3) with the corresponding halogen at elevated temperatures. Such compounds are susceptible to disproportionation reactions and are not stable in water.
Many chromium(II) compounds are known, such as the water-stable chromium(II) chloride CrCl
2 that can be made by reducing chromium(III) chloride with zinc. The resulting bright blue solution created from dissolving chromium(II) chloride is only stable at neutral pH. Some other notable chromium(II) compounds include chromium(II) oxide CrO, and chromium(II) sulfate CrSO
4. Many chromous carboxylates are known as well, the most famous of these being the red chromium(II) acetate (Cr2(O2CCH3)4) that features a quadruple bond.
Most chromium(I) compounds are obtained solely by oxidation of electron-rich, octahedral chromium(0) complexes. Other chromium(I) complexes contain cyclopentadienyl ligands. As verified by X-ray diffraction, a Cr-Cr quintuple bond (length 183.51(4) pm) has also been described. Extremely bulky monodentate ligands stabilize this compound by shielding the quintuple bond from further reactions.
Chromium is the 13th most abundant element in Earth's crust with an average concentration of 100 ppm. Chromium compounds are found in the environment from the erosion of chromium-containing rocks, and can be redistributed by volcanic eruptions. Typical background concentrations of chromium in environmental media are: atmosphere <10 ng m−3; soil <500 mg kg−1; vegetation <0.5 mg kg−1; freshwater <10 μg L−1; seawater <1 μg L−1; sediment <80 mg kg−1. Chromium is mined as chromite (FeCr2O4) ore.
About two-fifths of the chromite ores and concentrates in the world are produced in South Africa, about a third in Kazakhstan, while India, Russia, and Turkey are also substantial producers. Untapped chromite deposits are plentiful, but geographically concentrated in Kazakhstan and southern Africa. Although rare, deposits of native chromium exist. The Udachnaya Pipe in Russia produces samples of the native metal. This mine is a kimberlite pipe, rich in diamonds, and the reducing environment helped produce both elemental chromium and diamonds.
The relation between Cr(III) and Cr(VI) strongly depends on pH and oxidative properties of the location. In most cases, Cr(III) is the dominating species, but in some areas, the ground water can contain up to 39 µg/liter of total chromium of which 30 µg/liter is Cr(VI).
Chromium was first discovered as an element after it came to the attention of the Western world in the red crystalline mineral crocoite (which is lead(II) chromate). This mineral was discovered in 1761 and was initially used as a pigment; the distinctive color was attributed to the chromium from within the crocoite. In present day, nearly all chromium is commercially extracted from the only viable ore for extensiveness and predicted long term use, being chromite, which is iron chromium oxide (FeCr2O4); chromite is now the principal source of chromium for use in pigments.
Weapons found in burial pits dating from the late 3rd century B.C. Qin Dynasty of the Terracotta Army near Xi'an, China, have been analyzed by archaeologists. Although these weapons were presumably buried more than two millennia ago, the ancient bronze tips of both the swords and crossbow bolts found at the site showed unexpectedly little corrosion, possibly because the bronze was deliberately coated with a thin layer of chromium oxide. Still, this oxide layer that was found on the weapons was not pure chromium metal or chrome plating as it is commonly produced today, but a mere 10-15 μm layer of chromium oxide molecules at up to 2% chromium was discovered, which turned out to be enough to protect the bronze from corroding.
Chromium minerals as pigments came to the attention of the west in the 18th century. On 26 July 1761, Johann Gottlob Lehmann found an orange-red mineral in the Beryozovskoye mines in the Ural Mountains which he named Siberian red lead. Though misidentified as a lead compound with selenium and iron components, the mineral was in fact crocoite (or lead(II) chromate) with a formula of PbCrO4. In 1770, Peter Simon Pallas visited the same site as Lehmann and found a red lead mineral that was discovered to possess useful properties as a pigment in paints. After Pallas, the use of Siberian red lead as a paint pigment began to develop rapidly throughout the region.
In 1794, Louis Nicolas Vauquelin received samples of crocoite ore. He produced chromium trioxide (CrO3) by mixing crocoite with hydrochloric acid. In 1797, Vauquelin discovered that he could isolate metallic chromium by heating the oxide in a charcoal oven, for which he is credited as the one who truly discovered the element. Vauquelin was also able to detect traces of chromium in precious gemstones, such as ruby or emerald.
During the 19th century, chromium was primarily used not only as a component of paints, but in tanning salts as well. For quite some time, the crocoite found in Russia was the main source for such tanning materials. In 1827, a larger chromite deposit was discovered near Baltimore, United States, which quickly met the demand for tanning salts much more adequately than the crocoite that had been used previously. This made the United States the largest producer of chromium products until the year 1848, when larger deposits of chromite were uncovered near the city of Bursa, Turkey.
Chromium is also famous for its reflective, metallic luster when polished. It is used as a protective and decorative coating on car parts, plumbing fixtures, furniture parts and many other items, usually applied by electroplating. Chromium was used for electroplating as early as 1848, but this use only became widespread with the development of an improved process in 1924.
Approximately 28.8 million metric tons (Mt) of marketable chromite ore was produced in 2013, and converted into 7.5 Mt of ferrochromium. According to John F. Papp, writing for the USGS, "Ferrochromium is the leading end use of chromite ore, [and] stainless steel is the leading end use of ferrochromium."
The largest producers of chromium ore in 2013 have been South Africa (48%), Kazakhstan (13%), Turkey (11%), India (10%) with several other countries producing the rest of about 18% of the world production.
The two main products of chromium ore refining are ferrochromium and metallic chromium. For those products the ore smelter process differs considerably. For the production of ferrochromium, the chromite ore (FeCr2O4) is reduced in large scale in electric arc furnace or in smaller smelters with either aluminium or silicon in an aluminothermic reaction.
For the production of pure chromium, the iron must be separated from the chromium in a two step roasting and leaching process. The chromite ore is heated with a mixture of calcium carbonate and sodium carbonate in the presence of air. The chromium is oxidized to the hexavalent form, while the iron forms the stable Fe2O3. The subsequent leaching at higher elevated temperatures dissolves the chromates and leaves the insoluble iron oxide. The chromate is converted by sulfuric acid into the dichromate.
The dichromate is converted to the chromium(III) oxide by reduction with carbon and then reduced in an aluminothermic reaction to chromium.
The strengthening effect of forming stable metal carbides at the grain boundaries and the strong increase in corrosion resistance made chromium an important alloying material for steel. The high-speed tool steels contain between 3 and 5% chromium. Stainless steel, the primary corrosion-resistant metal alloy, is formed when chromium is introduced to iron in sufficient concentrations, usually where the chromium concentration is above 11%. For stainless steel's formation, ferrochromium is added to the molten iron. Also, nickel-based alloys increase in strength due to the formation of discrete, stable metal carbide particles at the grain boundaries. For example, Inconel 718 contains 18.6% chromium. Because of the excellent high-temperature properties of these nickel superalloys, they are used in jet engines and gas turbines in lieu of common structural materials.
The relative high hardness and corrosion resistance of unalloyed chromium makes chrome a reliable metal for surface coating; it is still the most popular metal for sheet coating with its above average durability compared to other coating metals. A layer of chromium is deposited on pretreated metallic surfaces by electroplating techniques. There are two deposition methods: thin and thick. Thin deposition involves a layer of chromium below 1 µm thickness deposited by chrome plating, and is used for decorative surfaces. Thicker chromium layers are deposited if wear-resistant surfaces are needed. Both methods use acidic chromate or dichromate solutions. To prevent the energy-consuming change in oxidation state, the use of chromium(III) sulfate is under development; for most applications of chromium, the previously established process is used.
In the chromate conversion coating process, the strong oxidative properties of chromates are used to deposit a protective oxide layer on metals like aluminium, zinc and cadmium. This passivation and the self-healing properties by the chromate stored in the chromate conversion coating, which is able to migrate to local defects, are the benefits of this coating method. Because of environmental and health regulations on chromates, alternative coating methods are under development.
Chromic acid anodizing (or Type I anodizing) of aluminium is another electrochemical process, which does not lead to the deposition of chromium, but uses chromic acid as electrolyte in the solution. During anodization, an oxide layer is formed on the aluminium. The use of chromic acid, instead of the normally used sulfuric acid, leads to a slight difference of these oxide layers. The high toxicity of Cr(VI) compounds, used in the established chromium electroplating process, and the strengthening of safety and environmental regulations demand a search for substitutes for chromium or at least a change to less toxic chromium(III) compounds.
The mineral crocoite (which is also lead chromate PbCrO4) was used as a yellow pigment shortly after its discovery. After a synthesis method became available starting from the more abundant chromite, chrome yellow was, together with cadmium yellow, one of the most used yellow pigments. The pigment does not photodegrade, but it tends to darken due to the formation of chromium(III) oxide. It has a strong color, and was used for school buses in the United States and for the Postal Service (for example, the Deutsche Post) in Europe. The use of chrome yellow has since declined due to environmental and safety concerns and was replaced by organic pigments or other alternatives that are free from lead and chromium. Other pigments that are based around chromium are, for example, the deep shade of red pigment chrome red, which is simply lead chromate with lead(II) hydroxide (PbCrO4·Pb(OH)2). A very important chromate pigment, which was used widely in metal primer formulations, was zinc chromate, now replaced by zinc phosphate. A wash primer was formulated to replace the dangerous practice of pre-treating aluminium aircraft bodies with a phosphoric acid solution. This used zinc tetroxychromate dispersed in a solution of polyvinyl butyral. An 8% solution of phosphoric acid in solvent was added just before application. It was found that an easily oxidized alcohol was an essential ingredient. A thin layer of about 10–15 µm was applied, which turned from yellow to dark green when it was cured. There is still a question as to the correct mechanism. Chrome green is a mixture of Prussian blue and chrome yellow, while the chrome oxide green is chromium(III) oxide.
Chromium oxides are also used as a green pigment in the field of glassmaking and also as a glaze for ceramics. Green chromium oxide is extremely lightfast and as such is used in cladding coatings. It is also the main ingredient in infrared reflecting paints, used by the armed forces to paint vehicles and to give them the same infrared reflectance as green leaves.
Natural rubies are corundum (aluminum oxide) crystals that are colored red (the rarest type) due to chromium (III) ions (other colors of corundum gems are termed sapphires). A red-colored artificial ruby may also be achieved by doping chromium(III) into artificial corundum crystals, thus making chromium a requirement for making synthetic rubies. Such a synthetic ruby crystal was the basis for the first laser, produced in 1960, which relied on stimulated emission of light from the chromium atoms in such a crystal. A ruby laser is lasing at 694.3 nanometers, in a deep red color.
Because of their toxicity, chromium(VI) salts are used for the preservation of wood. For example, chromated copper arsenate (CCA) is used in timber treatment to protect wood from decay fungi, wood-attacking insects, including termites, and marine borers. The formulations contain chromium based on the oxide CrO3 between 35.3% and 65.5%. In the United States, 65,300 metric tons of CCA solution were used in 1996.
Chromium(III) salts, especially chrome alum and chromium(III) sulfate, are used in the tanning of leather. The chromium(III) stabilizes the leather by cross linking the collagen fibers. Chromium tanned leather can contain between 4 and 5% of chromium, which is tightly bound to the proteins. Although the form of chromium used for tanning is not the toxic hexavalent variety, there remains interest in management of chromium in the tanning industry. Recovery and reuse, direct/indirect recycling, use of less chromium, or "chrome-less" tanning are practiced to better manage chromium in tanning.
The high heat resistivity and high melting point makes chromite and chromium(III) oxide a material for high temperature refractory applications, like blast furnaces, cement kilns, molds for the firing of bricks and as foundry sands for the casting of metals. In these applications, the refractory materials are made from mixtures of chromite and magnesite. The use is declining because of the environmental regulations due to the possibility of the formation of chromium(VI). 
Several chromium compounds are used as catalysts for processing hydrocarbons. For example, the Phillips catalyst, prepared from chromium oxides, is used for the production of about half the world's polyethylene. Fe-Cr mixed oxides are employed as high-temperature catalysts for the water gas shift reaction. Copper chromite is a useful hydrogenation catalyst.
The biologically beneficial effects of Chromium(III) continue to be debated. Some experts believe that they reflect pharmacological rather than nutritional responses, while others suggest that they are side effects of a toxic metal. The discussion is marred by elements of negativity and occasionally becomes acrimonious. Chromium is accepted by the U.S. National Institutes of Health as a trace element for its roles in the action of insulin, a hormone critical to the metabolism and storage of carbohydrate, fat and protein. The precise mechanism of its actions in the body, however, have not been fully defined, leaving in question whether chromium is essential for healthy people.
In contrast, hexavalent chromium (Cr(VI) or Cr6+) is highly toxic and mutagenic when inhaled. Ingestion of chromium(VI) in water has been linked to stomach tumors, and it may also cause allergic contact dermatitis (ACD).
Chromium deficiency, involving a lack of Cr(III) in the body, or perhaps some complex of it, such as glucose tolerance factor is controversial. Some studies suggest that the biologically active form of chromium (III) is transported in the body via an oligopeptide called low-molecular-weight chromium-binding substance (LMWCr), which might play a role in the insulin signaling pathway.
Chromium content of common foods is generally low (1-13 micrograms per serving). Chromium content of food varies widely due to differences in soil mineral content, growing season, plant cultivar, and contamination during processing. In addition, chromium (and nickel) leach into food cooked in stainless steel, with the effect largest when the cookware is new. Acidic foods such as tomato sauce which are cooked for many hours also exacerbate this effect.
There is disagreement on chromium's status as an essential nutrient. Governmental departments from Australia, New Zealand, India, Japan and the United States consider chromium essential while the European Food Safety Authority (EFSA), representing the European Union, does not.
The National Academy of Medicine (NAM) updated the Estimated Average Requirements (EARs) and the Recommended Dietary Allowances (RDAs) for chromium in 2001. For chromium, there was not sufficient information to set EARs and RDAs, so its needs are described as estimates for Adequate Intakes (AIs). The current AIs of chromium for women ages 14 through 50 is 25 μg/day, and the AIs for women ages 50 and above is 20 μg/day. The AIs for women who are pregnant are 30 μg/day, and for women who are lactating, the set AIs are 45 μg/day. The AIs for men ages 14 through 50 are 35 μg/day, and the AIs for men ages 50 and above are 30 μg/day. For children ages 1 through 13, the AIs increase with age from 0.2 μg/day up to 25 μg/day. As for safety, the NAM sets Tolerable Upper Intake Levels (ULs) for vitamins and minerals when the evidence is sufficient. In the case of chromium, there is not yet enough information and hence no UL has been established. Collectively, the EARs, RDAs, AIs and ULs are the parameters for the nutrition recommendation system known as Dietary Reference Intake (DRI). Australia and New Zealand consider chromium to be an essential nutrient, with an AI of 35 μg/day for men, 25 μg/day for women, 30 μg/day for women who are pregnant, and 45 μg/day for women who are lactating. A UL has not been set due to the lack of sufficient data. India considers chromium to be an essential nutrient, with an adult recommended intake of 33 μg/day. Japan also considers chromium to be an essential nutrient, with an AI of 10 μg/day for adults, including women who are pregnant or lactating. A UL has not been set. The EFSA of the European Union however, does not consider chromium to be an essential nutrient; chromium is the only mineral for which the United States and the European Union disagree.
For the United States' food and dietary supplement labeling purposes, the amount of the substance in a serving is expressed as a percent of the Daily Value (%DV). For chromium labeling purposes, 100% of the Daily Value was 120 μg. As of May 27, 2016, the percentage of daily value was revised to 35 μg to bring the chromium intake into a consensus with the official Recommended Dietary Allowance. The original deadline to be in compliance was July 28, 2018, but on September 29, 2017 the Food and Drug Administration released a proposed rule that extended the deadline to January 1, 2020 for large companies and January 1, 2021 for small companies.
Food composition databases such as the those maintained by the U.S. Department of Agriculture do not contain information on the chromium content of foods. A wide variety of animal-sourced and vegetable-sourced foods contain chromium. Content per serving is influenced by the chromium content of the soil in which the plants are grown and by feedstuffs fed to animals; also by processing methods, as chromium is leached into foods if processed or cooked in chromium-containing stainless steel equipment. One diet analysis study conducted in Mexico reported an average daily chromium intake of 30 micrograms. An estimated 31% of adults in the United States consume multi-vitamin/mineral dietary supplements which often contain 25 to 60 micrograms of chromium.
Chromium is an ingredient in total parenteral nutrition (TPN) because deficiency can occur after months of intravenous feeding with chromium-free TPN. For this reason, chromium is added to TPN solutions, along with other trace minerals. It is also in nutritional products for preterm infants. Although the mechanism in biological roles for chromium is unclear, in the United States chromium-containing products are sold as non-prescription dietary supplements in amounts ranging from 50 to 1,000 μg. Lower amounts of chromium are also often incorporated into multi-vitamin/mineral supplements consumed by an estimated 31% of adults in the United States. Chemical compounds used in dietary supplements include chromium chloride, chromium citrate, chromium(III) picolinate, chromium(III) polynicotinate, and other chemical compositions. The benefit of supplements has not been proven.
In 2005, the U.S. Food and Drug Administration had approved a Qualified Health Claim for chromium picolinate with a requirement for very specific label wording: "One small study suggests that chromium picolinate may reduce the risk of insulin resistance, and therefore possibly may reduce the risk of type 2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type 2 diabetes is highly uncertain." At the same time, in answer to other parts of the petition, the FDA rejected claims for chromium picolinate and cardiovascular disease, retinopathy or kidney disease caused be abnormally high blood sugar levels. In 2010, chromium(III) picolinate was approved by Health Canada to be used in dietary supplements. Approved labeling statements include: a factor in the maintenance of good health, provides support for healthy glucose metabolism, helps the body to metabolize carbohydrates and helps the body to metabolize fats. The European Food Safety Authority (EFSA) approved claims in 2010 that chromium contributed to normal macronutrient metabolism and maintenance of normal blood glucose concentration, but rejected claims for maintenance or achievement of a normal body weight, or reduction of tiredness or fatigue.
Given the evidence for chromium deficiency causing problems with glucose management in the context of intravenous nutrition products formulated without chromium, research interest turned to whether chromium supplementation for people who have type 2 diabetes but are not chromium deficient could benefit. Looking at the results from four meta-analyses, one reported a statistically significant decrease in fasting plasma glucose levels (FPG) and a non-significant trend in lower hemoglobin A1C. A second reported the same, a third reported significant decreases for both measures, while a fourth reported no benefit for either. A review published in 2016 listed 53 randomized clinical trials that were included in one or more of six meta-analyses. It concluded that whereas there may be modest decreases in FPG and/or HbA1C that achieve statistical significance in some of these meta-analyses, few of the trials achieved decreases large enough to be expected to be relevant to clinical outcome.
Two systematic reviews looked at chromium supplements as a mean of managing body weight in overweight and obese people. One, limited to chromium picolinate, a popular supplement ingredient, reported a statistically significant -1.1 kg (2.4 lb) weight loss in trials longer than 12 weeks. The other included all chromium compounds and reported a statistically significant -0.50 kg (1.1 lb) weight change. Change in percent body fat did not reach statistical significance. Authors of both reviews considered the clinical relevance of this modest weight loss as uncertain/unreliable. The European Food Safety Authority reviewed the literature and concluded that there was insufficient evidence to support a claim.
Chromium is promoted as a sports performance dietary supplement, based on the theory that it potentiated insulin activity, with anticipated results of increased muscle mass, and faster recovery of glycogen storage during post-exercise recovery. A review of clinical trials reported that chromium supplementation did not improve exercise performance or increase muscle strength. The International Olympic Committee reviewed dietary supplements for high-performance athletes in 2018 and concluded there was no need to increase chromium intake for athletes, nor support for claims of losing body fat.
Chromium is naturally present in the environment in trace amounts, but industrial use in rubber and stainless steel manufacturing, chrome plating, dyes for textiles, tanneries and other uses contaminates aquatic systems. In Bangladesh, rivers in or downstream from industrialized areas exhibit heavy metal contamination. Irrigation water standards for chromium are 0.1 mg/L, but some rivers are more than five times that amount. The standard for fish for human consumption is less than 1 mg/kg, but many tested samples were more than five times that amount. Chromium, especially hexavalent chromium, is highly toxic to fish because it is easily absorbed across the gills, readily enters blood circulation, crosses cell membranes and bioconcentrates up the food chain. In contrast, the toxicity of trivalent chromium is very low, attributed to poor membrane permeability and little biomagnification.
Acute and chronic exposure to chromium(VI) affect fish behavior, physiology, reproduction and survival. Hyperactivity and erratic swimming have been reported in contaminated environments. Egg hatching and fingerling survival are affected. In adult fish there are reports of histopathological damage to liver, kidney, muscle, intestines, and gills. Mechanisms include mutagenic gene damage and disruptions of enzyme functions.
There is evidence that fish may not require chromium, but benefit from a measured amount in diet. In one study, juvenile fish gained weight on a zero chromium diet, but the addition of 500 μg of chromium in the form of chromium chloride or other supplement types, per kilogram of food (dry weight), increased weight gain. At 2,000 μg/kg the weight gain was no better than with the zero chromium diet, and there were increased DNA strand breaks.
Water-insoluble chromium(III) compounds and chromium metal are not considered a health hazard, while the toxicity and carcinogenic properties of chromium(VI) have been known for a long time. Because of the specific transport mechanisms, only limited amounts of chromium(III) enter the cells. Acute oral toxicity ranges between 1.5 and 3.3 mg/kg. A 2008 review suggested that moderate uptake of chromium(III) through dietary supplements poses no genetic-toxic risk. In the US, the Occupational Safety and Health Administration (OSHA) has designated an air permissible exposure limit (PEL) in the workplace as a time-weighted average (TWA) of 1 mg/m3. The National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 0.5 mg/m3, time-weighted average. The IDLH (immediately dangerous to life and health) value is 250 mg/m3.
The acute oral toxicity for chromium(VI) ranges between 50 and 150 mg/kg. In the body, chromium(VI) is reduced by several mechanisms to chromium(III) already in the blood before it enters the cells. The chromium(III) is excreted from the body, whereas the chromate ion is transferred into the cell by a transport mechanism, by which also sulfate and phosphate ions enter the cell. The acute toxicity of chromium(VI) is due to its strong oxidant properties. After it reaches the blood stream, it damages the kidneys, the liver and blood cells through oxidation reactions. Hemolysis, renal, and liver failure result. Aggressive dialysis can be therapeutic.
The carcinogenity of chromate dust has been known for a long time, and in 1890 the first publication described the elevated cancer risk of workers in a chromate dye company. Three mechanisms have been proposed to describe the genotoxicity of chromium(VI). The first mechanism includes highly reactive hydroxyl radicals and other reactive radicals which are by products of the reduction of chromium(VI) to chromium(III). The second process includes the direct binding of chromium(V), produced by reduction in the cell, and chromium(IV) compounds to the DNA. The last mechanism attributed the genotoxicity to the binding to the DNA of the end product of the chromium(III) reduction.
Chromium salts (chromates) are also the cause of allergic reactions in some people. Chromates are often used to manufacture, amongst other things, leather products, paints, cement, mortar and anti-corrosives. Contact with products containing chromates can lead to allergic contact dermatitis and irritant dermatitis, resulting in ulceration of the skin, sometimes referred to as "chrome ulcers". This condition is often found in workers that have been exposed to strong chromate solutions in electroplating, tanning and chrome-producing manufacturers.
Because chromium compounds were used in dyes, paints, and leather tanning compounds, these compounds are often found in soil and groundwater at active and abandoned industrial sites, needing environmental cleanup and remediation. Primer paint containing hexavalent chromium is still widely used for aerospace and automobile refinishing applications.
In 2010, the Environmental Working Group studied the drinking water in 35 American cities in the first nationwide study. The study found measurable hexavalent chromium in the tap water of 31 of the cities sampled, with Norman, Oklahoma, at the top of list; 25 cities had levels that exceeded California's proposed limit.
Blink is a browser engine used in the Google Chrome browser and many other projects. It is developed as part of the Chromium project with contributions from Google, Opera Software ASA, Adobe Systems, Intel, Samsung and others. It was first announced in April 2013.Chrome OS
Chrome OS is a Linux kernel-based operating system designed by Google. It is derived from the free software Chromium OS and uses the Google Chrome web browser as its principal user interface. As a result, Chrome OS primarily supports web applications.Google announced the project in July 2009, conceiving it as an operating system in which both applications and user data reside in the cloud: hence Chrome OS primarily runs web applications. Source code and a public demo came that November. The first Chrome OS laptop, known as a Chromebook, arrived in May 2011. Initial Chromebook shipments from Samsung and Acer occurred in July 2011.
Chrome OS has an integrated media player and file manager. It supports Chrome Apps, which resemble native applications, as well as remote access to the desktop. Android applications started to become available for the operating system in 2014, and in 2016, access to Android apps in the entire Google Play Store was introduced on supported Chrome OS devices. Reception was initially skeptical, with some observers arguing that a browser running on any operating system was functionally equivalent. As more Chrome OS machines have entered the market, the operating system is now seldom evaluated apart from the hardware that runs it.
Chrome OS is only available pre-installed on hardware from Google manufacturing partners, but there are unofficial methods that allow it to be installed in other equipment. An open source equivalent, Chromium OS, can be compiled from downloaded source code. Early on, Google provided design goals for Chrome OS, but has not otherwise released a technical description.Chrome plating
Chrome plating (less commonly chromium plating), often referred to simply as chrome, is a technique of electroplating a thin layer of chromium onto a metal object. The chromed layer can be decorative, provide corrosion resistance, ease cleaning procedures, or increase surface hardness. Sometimes, a less expensive imitator of chrome may be used for aesthetic purposes.Chromium(II) fluoride
Chromium(II) fluoride is an inorganic compound with the formula CrF2. It exists as a blue-green iridescent solid. Chromium(II) fluoride is sparingly soluble in water, almost insoluble in alcohol, and is soluble in boiling hydrochloric acid, but is not attacked by hot distilled sulfuric acid or nitric acid. Like other chromous compounds, chromium(II) fluoride is oxidized to chromium(III) oxide in air.Chromium(III) chloride
Chromium(III) chloride (also called chromic chloride) describes any of several compounds of with the formula CrCl3 · xH2O, where x can be 0, 5, and 6. The anhydrous compound with the formula CrCl3 is a violet solid. The most common form of the trichloride is the dark green "hexahydrate", CrCl3 · 6H2O. Chromium chloride finds uses as catalysts and as precursors to dyes for wool.Chromium(III) oxide
Chromium(III) oxide (or chromia) is the inorganic compound of the formula Cr2O3. It is one of the principal oxides of chromium and is used as a pigment. In nature, it occurs as the rare mineral eskolaite.Chromium(IV) oxide
Chromium dioxide or chromium(IV) oxide is an inorganic compound with the formula CrO2. It is a black synthetic magnetic solid. It once was widely used in magnetic tape emulsion. With the increasing popularity of CDs and DVDs, the use of chromium(IV) oxide has declined. However, it is still used in data tape applications for enterprise-class storage systems. It is still considered by many oxide and tape manufacturers to have been one of the best magnetic recording particulates ever invented.Chromium (web browser)
Chromium is Google's open-source web browser project. It is a fully functional browser on its own and supplies the vast majority of code for the Google Chrome browser. The two browsers have always had some differences, as indicated by their names: chromium is the metal used to make chrome plating.The Chromium code is also widely used by other parties to create their own browsers. Many vendors use the code in a similar manner as Google, while others simply build it as-is and release browsers with the Chromium name.
The user interface is minimalist because Google wanted its browser to "feel lightweight (cognitively and physically) and fast".Chromium OS
Chromium OS is an open-source operating system designed for running web applications and browsing the World Wide Web. It is the development version of Chrome OS, a Linux distribution made by Google.
Like Chrome OS, Chromium OS is based on the Linux kernel, but its principal user interface is the Chromium web browser rather than the Google Chrome browser. Chromium also includes the Portage package manager, which was originally developed for Gentoo Linux. Because Chromium OS and Chrome OS use a web browser engine for the user interface, they are oriented toward web applications rather than desktop applications or mobile apps.Google first published the Chromium OS source code in late 2009.Chromium pentafluoride
Chromium pentafluoride is the inorganic compound with the chemical formula CrF5. It is a red volatile solid that melts at 30 °C, which easily hydrolyses to chromium(III) and chromium(VI). It has the same crystal structure as vanadium pentafluoride. It is the highest known chromium fluoride, since the hypothetical chromium hexafluoride has not yet been synthesized.Chromium pentafluoride is one of the products of the action of fluorine on a mixture of potassium and chromic chlorides.In terms of its structure, the compound is a one-dimensional coordination polymer. Each Cr(V) center has octahedral molecular geometry.Chromium trifluoride
Chromium(III) fluoride is the name for the inorganic compounds with the chemical formula CrF3 as well as several related hydrates. The compound CrF3 is a green crystalline solid that is insoluble in common solvents, but the coloured hydrates [Cr(H2O)6]F3 and [Cr(H2O)6]F3•3H2O are soluble in water. The trihydrate is green, and the hexahydrate is violet. The anhydrous form sublimes at 1100–1200 °C.Chromium trioxide
Chromium trioxide is an inorganic compound with the formula CrO3. It is the acidic anhydride of chromic acid, and is sometimes marketed under the same name.
This compound is a dark-purple solid under anhydrous conditions, bright orange when wet and which dissolves in water concomitant with hydrolysis. Millions of kilograms are produced annually, mainly for electroplating. Chromium trioxide is a powerful oxidiser and a suspected carcinogen.Google Chrome
Google Chrome (commonly known simply as Chrome) is a cross-platform web browser developed by Google. It was first released in 2008 for Microsoft Windows, and was later ported to Linux, macOS, iOS, and Android. The browser is also the main component of Chrome OS, where it serves as the platform for web apps.
Most of Chrome's source code comes from Google's open-source Chromium project, but Chrome is licensed as proprietary freeware. WebKit was the original rendering engine, but Google eventually forked it to create the Blink engine; all Chrome variants except iOS now use Blink.As of February 2019, StatCounter estimates that Chrome has a 62% worldwide browser market share across all platforms. Because of this success, Google has expanded the "Chrome" brand name to other products: Chrome OS, Chromecast, Chromebook, Chromebit, Chromebox, and Chromebase.Group 6 element
Group 6, numbered by IUPAC style, is a group of elements in the periodic table. Its members are chromium (Cr), molybdenum (Mo), tungsten (W), and seaborgium (Sg). These are all transition metals and chromium, molybdenum and tungsten are refractory metals. The period 8 elements of group 6 are likely to be either unpenthexium (Uph) or unpentoctium (Upo). This may not be possible; drip instability may imply that the periodic table ends around unbihexium. Neither unpenthexium nor unpentoctium have been synthesized, and it is unlikely that this will happen in the near future.
Like other groups, the members of this family show patterns in its electron configuration, especially the outermost shells resulting in trends in chemical behavior:
"Group 6" is the new IUPAC name for this group; the old style name was "group VIB" in the old US system (CAS) or "group VIA" in the European system (old IUPAC). Group 6 must not be confused with the group with the old-style group crossed names of either VIA (US system, CAS) or VIB (European system, old IUPAC). That group is now called group 16.Hexavalent chromium
Hexavalent chromium (chromium(VI), Cr(VI), chromium 6) is any chemical compound that contains the element chromium in the +6 oxidation state (thus hexavalent). Virtually all chromium ore is processed via hexavalent chromium, specifically the salt sodium dichromate. Approximately 136,000 tonnes (300,000,000 lb) of hexavalent chromium were produced in 1985. Additional hexavalent chromium compounds are chromium trioxide and various salts of chromate and dichromate, among others. Hexavalent chromium is used in textile dyes, wood preservation, anti-corrosion products, chromate conversion coatings, and a variety of niche uses. Industrial uses of hexavalent chromium compounds include chromate pigments in dyes, paints, inks, and plastics; chromates added as anticorrosive agents to paints, primers, and other surface coatings; and chromic acid electroplated onto metal parts to provide a decorative or protective coating. Hexavalent chromium can be formed when performing "hot work" such as welding on stainless steel or melting chromium metal. In these situations the chromium is not originally hexavalent, but the high temperatures involved in the process result in oxidation that converts the chromium to a hexavalent state. Hexavalent chromium can also be found in drinking water and public water systems.Inhaled hexavalent chromium is recognized as a human carcinogen. Workers in many occupations are exposed to hexavalent chromium. Problematic exposure is known to occur among workers who handle chromate-containing products and those who grind and/ or weld stainless steel. Workers who are exposed to hexavalent chromium are at increased risk of developing lung cancer, asthma, or damage to the nasal epithelia and skin. Within the European Union, the use of hexavalent chromium in electronic equipment is largely prohibited by the Restriction of Hazardous Substances Directive.Isotopes of chromium
Naturally occurring chromium (24Cr) is composed of four stable isotopes; 50Cr, 52Cr, 53Cr, and 54Cr with 52Cr being the most abundant (83.789% natural abundance). 50Cr is suspected of decaying by β+β+ to 50Ti with a half-life of (more than) 1.8×1017 years. Twenty-two radioisotopes, all of which are entirely synthetic, have been characterized with the most stable being 51Cr with a half-life of 27.7 days. All of the remaining radioactive isotopes have half-lives that are less than 24 hours and the majority of these have half-lives that are less than 1 minute, the least stable being 66Cr with a half-life of 10 milliseconds. This element also has 2 meta states, 45mCr, the more stable one, and 59mCr, the least stable isotope or isomer.
53Cr is the radiogenic decay product of 53Mn. Chromium isotopic contents are typically combined with manganese isotopic contents and have found application in isotope geology. Mn-Cr isotope ratios reinforce the evidence from 26Al and 107Pd for the early history of the solar system. Variations in 53Cr/52Cr and Mn/Cr ratios from several meteorites indicate an initial 53Mn/55Mn ratio that suggests Mn-Cr isotope systematics must result from in-situ decay of 53Mn in differentiated planetary bodies. Hence 53Cr provides additional evidence for nucleosynthetic processes immediately before coalescence of the solar system. The same isotope is preferentially involved in certain leaching reactions, thereby allowing its abundance in seawater sediments to be used as a proxy for atmospheric oxygen concentrations.The isotopes of chromium range from 42Cr to 67Cr. The primary decay mode before the most abundant stable isotope, 52Cr, is electron capture and the primary mode after is beta decay.Leather
Leather is a natural durable and flexible material created by tanning animal rawhides and skins. The most common raw material is cattle hide. It can be produced at manufacturing scales ranging from artisan to modern industrial scale.
Leather is used to make a variety of articles, including footwear, automobile seats, clothing, bags, book bindings, fashion accessories, and furniture. It is produced in a wide variety of types and styles and decorated by a wide range of techniques. The earliest record of leather artifacts dates back to 2200 BC.Stainless steel
In metallurgy, stainless steel, also known as inox steel or inox from French inoxydable (inoxidizable), is a steel alloy, with highest percentage contents of iron, chromium, and nickel, with a minimum of 10.5% chromium content by mass and a maximum of 1.2% carbon by mass.Stainless steels are most notable for their corrosion resistance, which increases with increasing chromium content. Additions of molybdenum increase corrosion resistance in reducing acids and against pitting attack in chloride solutions. Thus, there are numerous grades of stainless steel with varying chromium and molybdenum contents to suit the environment the alloy must endure. Stainless steel's resistance to corrosion and staining, low maintenance, and familiar luster make it an ideal material for many applications where both the strength of steel and corrosion resistance are required.
Stainless steels are rolled into sheets, plates, bars, wire, and tubing to be used in: cookware, cutlery, surgical instruments, major appliances; construction material in large buildings, such as the Chrysler Building; industrial equipment (for example, in paper mills, chemical plants, water treatment); and storage tanks and tankers for chemicals and food products (for example, chemical tankers and road tankers). Stainless steel's corrosion resistance, the ease with which it can be steam cleaned and sterilized, and no need for surface coatings has also influenced its use in commercial kitchens and food processing plants.Tanning (leather)
Tanning is the process of treating skins and hides of animals to produce leather. A tannery is the place where the skins are processed.
Tanning hide into leather involves a process which permanently alters the protein structure of skin, making it more durable and less susceptible to decomposition, and also possibly coloring it.
Before tanning, the skins are unhaired, degreased, desalted and soaked in water over a period of 6 hours to 2 days. Historically this process was considered a noxious or "odoriferous trade" and relegated to the outskirts of town.
Traditionally, tanning used tannin, an acidic chemical compound from which the tanning process draws its name (tannin is in turn named after an old German word for oak or fir trees, from which the compound was derived). The use of a chromium (III) solution was adopted by tanners in the Industrial Revolution.