Chromium is valued 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. Chromium is also greatly valued as a metal that is able to be highly polished while resisting tarnishing. Polished chromium reflects almost 70% of the visible spectrum, and almost 90% of infrared light.[11] The name of the element is derived from the Greek word χρῶμα, chrōma, meaning color,[12] because many chromium compounds are intensely colored.
Industrial production of chromium proceeds from chromite ore (mostly FeCr2O4) to produce ferrochromium, an iron-chromium alloy, by means of aluminothermic or silicothermic reactions. Ferrochromium is then used to produce alloys such as stainless steel. Pure chromium metal is produced by a different process: roasting and leaching of chromite to separate it from iron, followed by reduction with carbon and then aluminium.
Trivalent chromium (Cr(III)) occurs naturally in many foods and is sold as a dietary supplement, although there is insufficient evidence that dietary chromium provides nutritional benefit to people.[13][14] In 2014, the European Food Safety Authority concluded that research on dietary chromium did not justify it to be recognized as an essential nutrient.[15]
While chromium metal and Cr(III) ions are considered non-toxic, chromate and its derivatives, often called "hexavalent chromium", is toxic and carcinogenic. According to the European Chemicals Agency (ECHA), chromium trioxide that is used in industrial electroplating processes is a "substance of very high concern" (SVHC).[16]
Physical properties
Atomic
Gaseous chromium has a ground-state electron configuration of [ Ar] 3d5 4s1. It is the first element in the periodic table whose configuration violates the Aufbau principle. Exceptions to the principle also occur later in the periodic table for elements such as copper, niobium and molybdenum.[17]
Chromium is the first element in the 3d series where the 3d electrons start to sink into the 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.[18]
Bulk
Sample of chromium metal
Chromium is the third hardest element after 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 high specular reflection in comparison to other transition metals. In infrared, at 425μm, chromium has a maximum reflectance of about 72%, reducing to a minimum of 62% at 750μm before rising again to 90% at 4000μm.[11] When chromium is used in stainless steel alloys and polished, the specular reflection decreases with the inclusion of additional metals, yet is still high in comparison with other alloys. Between 40% and 60% of the visible spectrum is reflected from polished stainless steel.[11] The explanation on why chromium displays such a high turnout of reflected photon waves in general, especially the 90% in infrared, can be attributed to chromium's magnetic properties.[19] Chromium has unique magnetic properties; it is the only elemental solid that shows antiferromagnetic ordering at room temperature and below. Above 38°C, its magnetic ordering becomes paramagnetic.[7] 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 magnetic moments at the cube's corners and the unequal, but antiparallel, cube centers.[19] From here, the frequency-dependent relative permittivity of chromium, deriving from Maxwell's equations and chromium's antiferromagnetism, leaves chromium with a high infrared and visible light reflectance.[20]
Passivation
Chromium metal in air is passivated: it forms a thin, protective surface layer of chromium oxide with the corundum structure. 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.[21]
The surface chromiaCr2O3 scale, is adherent to the metal. In contrast, iron forms a more porous oxide which is weak and flakes easily and exposes fresh metal to the air, causing continued rusting. At room temperature, the chromia scale is a few atomic layers thick, growing in thickness by outward diffusion of metal ions across the scale. Above 950 °C volatile chromium trioxideCrO3 forms from the chromia scale, limiting the scale thickness and oxidation protection.[22]
Chromium, unlike 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.[23]
Naturally occurring chromium is composed of four stable isotopes; 50Cr, 52Cr, 53Cr and 54Cr, with 52Cr being the most abundant (83.789% natural abundance). 50Cr is observationally stable, as it is theoretically capable of decaying to 50Ti via double electron capture with a half-life of no less than 1.3×1018 years. Twenty-five radioisotopes have been characterized, ranging from 42Cr to 70Cr; the most stable radioisotope is 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 metastablenuclear isomers.[9] The primary decay mode before the most abundant stable isotope, 52Cr, is electron capture and the primary mode after is beta decay.[9]
53Cr is the radiogenic decay product of 53Mn (half-life 3.74million years).[24] 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.[25]53Cr has been posited as a proxy for atmospheric oxygen concentration.[26]
The Pourbaix diagram for chromium in pure water, perchloric acid, or sodium hydroxide
Chromium is a member of group 6, of the transition metals. The +3 and +6 states occur most commonly within chromium compounds, followed by +2; charges of +1, +4 and +5 for chromium are rare, but do nevertheless occasionally exist.[29][30]
Chromium(II) compounds are uncommon, in part because they readily oxidize to chromium(III) derivatives in air. Water-stable chromium(II) chlorideCrCl 2 that can be made by reducing chromium(III) chloride with zinc. The resulting bright blue solution created from dissolving chromium(II) chloride is stable at neutral pH.[21] Some other notable chromium(II) compounds include chromium(II) oxideCrO, and chromium(II) sulfateCrSO 4. Many chromium(II) carboxylates are known. The red chromium(II) acetate (Cr2(O2CCH3)4) is somewhat famous. It features a Cr-Cr quadruple bond.[32]
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 anhydrous violet[35]chromium(III) chloride is dissolved in water, the violet solution turns green 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. A tetrahedral coordination of chromium(III) has been reported for the Cr-centered Keggin anion [α-CrW12O40]5–.[36]
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) 6]3− . 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.[21]
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:
2 [CrO4]2− + 2 H+⇌ [Cr2O7]2− + H2O
Chromium(VI) oxyhalides are known also and include chromyl fluoride (CrO2F2) and chromyl chloride (CrO 2Cl 2).[21] However, despite several erroneous claims, chromium hexafluoride (as well as all higher hexahalides) remains unknown, as of 2020.[37]
Chromium(VI) oxide
Sodium chromate is produced industrially by the oxidative roasting of chromite ore with 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.
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 5·OR 2.[21]
Chromic acid has the hypothetical formula H 2CrO 4. It is a vaguely described chemical, despite many well-defined chromates and dichromates being known. The dark red chromium(VI) oxideCrO 3, the acid anhydride of chromic acid, is sold industrially as "chromic acid".[21] It can be produced by mixing sulfuric acid with dichromate and is a strong oxidizing agent.
Compounds of chromium(V) are rather rare; 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.[38]
Compounds of chromium(IV) 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. Organic compounds containing Cr(IV) state such as chromium tetra t-butoxide are also known.[39]
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.[40] Extremely bulky monodentate ligands stabilize this compound by shielding the quintuple bond from further reactions.
Chromium compound determined experimentally to contain a Cr-Cr quintuple bond
Chromium is the 21st most abundant element in Earth's crust[41] with an average concentration of 100ppm. 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 <10ng/m3; soil <500mg/kg; vegetation <0.5mg/kg; freshwater <10μg/L; seawater <1μg/L; sediment <80mg/kg.[42] Chromium is mined as chromite (FeCr2O4) ore.[43]
About two-fifths of the chromite ores and concentrates in the world are produced in South Africa, about a third in Kazakhstan,[44] while India, Russia, and Turkey are also substantial producers. Untapped chromite deposits are plentiful, but geographically concentrated in Kazakhstan and southern Africa.[45] Although rare, deposits of native chromium exist.[46][47] 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.[48]
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,[27] but in some areas, the ground water can contain up to 39μg/L of total chromium, of which 30μg/L is Cr(VI).[49]
History
Early applications
Chromium minerals as pigments came to the attention of the west in the eighteenth century. On 26July 1761, Johann Gottlob Lehmann found an orange-red mineral in the Beryozovskoye mines in the Ural Mountains which he named Siberian red lead.[50][51] Though misidentified as a lead compound with selenium and iron components, the mineral was in fact crocoite with a formula of PbCrO4.[52] 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.[53] Crocoite would be the principal source of chromium in pigments until the discovery of chromite many years later.[54]
The red color of rubies is due to trace amounts of chromium within the corundum.
In 1794, Louis Nicolas Vauquelin received samples of crocoite ore. He produced chromium trioxide (CrO3) by mixing crocoite with hydrochloric acid.[52] 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.[55][56] Vauquelin was also able to detect traces of chromium in precious gemstones, such as ruby and emerald.[52][57]
During the nineteenth 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.[58] 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.[43] With the development of metallurgy and chemical industries in the Western world, the need for chromium increased.[59]
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.[60]
Production
Piece of chromium produced with aluminothermic reactionWorld production trend of chromiumChromium, remelted in a horizontal arc zone-refiner, showing large visible crystal grains
Approximately 28.8 million metric tons (Mt) of marketable chromite ore was produced in 2013, and converted into 7.5 Mt of ferrochromium.[45] 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."[45]
The largest producers of chromium ore in 2013 have been South Africa (48%), Kazakhstan (13%), Turkey (11%), and India (10%), with several other countries producing the rest of about 18% of the world production.[45]
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.[61]
Chromium ore output in 2002
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.[61]
The dichromate is converted to the chromium(III) oxide by reduction with carbon and then reduced in an aluminothermic reaction to chromium.[61]
Na2Cr2O7 + 2 C → Cr2O3 + Na2CO3 + CO
Cr2O3 + 2 Al → Al2O3 + 2 Cr
Applications
The creation of metal alloys account for 85% of the available chromium's usage. The remainder of chromium is used in the chemical, refractory, and foundry industries.[63]
Metallurgy
Stainless steel cutlery made from Cromargan 18/10, containing 18% chromium
The strengthening effect of forming stable metal carbides at grain boundaries, and the strong increase in corrosion resistance made chromium an important alloying material for steel. High-speed tool steels contain 3–5% chromium. Stainless steel, the primary corrosion-resistant metal alloy, is formed when chromium is introduced to iron in concentrations above 11%.[64] For stainless steel's formation, ferrochromium is added to the molten iron. Also, nickel-based alloys have increased 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.[65]ASTM B163 relies on chromium for condenser and heat-exchanger tubes, while castings with high strength at elevated temperatures that contain chromium are standardised with ASTM A567.[66]AISI type 332 is used where high temperature would normally cause carburization, oxidation or corrosion.[67]Incoloy 800 "is capable of remaining stable and maintaining its austenitic structure even after long time exposures to high temperatures".[68]Nichrome is used as resistance wire for heating elements in things like toasters and space heaters. These uses make chromium a strategic material. Consequently, during World War II, U.S. road engineers were instructed to avoid chromium in yellow road paint, as it "may become a critical material during the emergency".[69] The United States likewise considered chromium "essential for the German war industry" and made intense diplomatic efforts to keep it out of the hands of Nazi Germany.[70]
Decorative chrome plating on a motorcycle
The high hardness and corrosion resistance of unalloyed chromium makes it 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.[71] 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 1μm 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.[60]
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 of the chromate stored in the chromate conversion coating, which is able to migrate to local defects, are the benefits of this coating method.[72] Because of environmental and health regulations on chromates, alternative coating methods are under development.[73]
Chromic acid anodizing (or Type I anodizing) of aluminium is another electrochemical process that does not lead to the deposition of chromium, but uses chromic acid as an 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.[74] 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.[60]
Pigment
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 services (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 10–15μm 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.[75]
Chromium oxides are also used as a green pigment in the field of glassmaking and also as a glaze for ceramics.[76] 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.[77]
Other uses
Red crystal of a ruby laser
Chromium(III) ions present in corundum crystals (aluminium oxide) cause them to be colored red; when corundum appears as such, it is known as a ruby. If the corundum is lacking in chromium(III) ions, it is known as a sapphire.[note 3] 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.[note 4][78] 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. Ruby has a laser transition at 694.3 nanometers, in a deep red color.[79]
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.[80] 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.[80]
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.[81] Chromium tanned leather can contain 4–5% of chromium, which is tightly bound to the proteins.[43] 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,[82] and "chrome-less" or "chrome-free" tanning are practiced to better manage chromium usage.[83]
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).[61][84]
Chromic acid is a powerful oxidizing agent and is a useful compound for cleaning laboratory glassware of any trace of organic compounds.[92] It is prepared by dissolving potassium dichromate in concentrated sulfuric acid, which is then used to wash the apparatus. Sodium dichromate is sometimes used because of its higher solubility (50g/L versus 200g/L respectively). The use of dichromate cleaning solutions is now phased out due to the high toxicity and environmental concerns. Modern cleaning solutions are highly effective and chromium free.[93]
The possible nutritional value of chromium(III) is unproven.[97][98] Although chromium is regarded as a trace element and dietary mineral, its suspected roles in the action of insulin– a hormone that mediates the metabolism and storage of carbohydrate, fat, and protein – have not been adequately established.[13][14] The mechanism of its actions in the body is undefined, leaving in doubt whether chromium has a biological role in healthy people.[13][14][15]
"Chromium deficiency", involving a lack of Cr(III) in the body, or perhaps some complex of it, such as glucose tolerance factor, is not accepted as a medical condition, as it has no symptoms and healthy people do not require chromium supplementation.[13][14] 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 (chromodulin), which might play a role in the insulin signaling pathway.[13][101]
The chromium content of common foods is generally low (1–13 micrograms per serving).[13][102] The chromium content of food varies widely, due to differences in soil mineral content, growing season, plant cultivar, and contamination during processing.[14][102] Chromium (and nickel) leach into food cooked in stainless steel, with the effect being largest when the cookware is new. Acidic foods that are cooked for many hours also exacerbate this effect.[103][104]
There is disagreement on chromium's status as an essential nutrient. Governmental departments from Australia, New Zealand, India, and Japan consider chromium as essential,[105][106][107] while the United States and European Food Safety Authority of the European Union do not.[13][15]
The U.S. 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 insufficient information to set EARs and RDAs, so its needs are described as estimates for Adequate Intake (AI). From a 2001 assessment, AI of chromium for women ages 14 through 50 is 25μg/day, and the AI for women ages 50 and above is 20μg/day. The AIs for women who are pregnant are 30μg/day, and for women who are lactating, the set AI is 45μg/day. The AI for men ages 14 through 50 is 35μg/day, and the AI for men ages 50 and above is 30μg/day. For children ages 1 through 13, the AI increases with age from 0.2μg/day up to 25μg/day.[13] 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, 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).[108]
Australia and New Zealand consider chromium to be an essential nutrient, with an AI of 35μg/day for men, 25μg/day for women, 30μg/day for women who are pregnant, and 45μg/day for women who are lactating. A UL has not been set due to the lack of sufficient data.[105] India considers chromium to be an essential nutrient, with an adult recommended intake of 33μg/day.[106] Japan also considers chromium to be an essential nutrient, with an AI of 10μg/day for adults, including women who are pregnant or lactating. A UL has not been set.[107]
The EFSA does not consider chromium to be an essential nutrient.[15][109][110]
Labeling
For U.S. 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 120μg. As of 27May 2016, the percentage of daily value was revised to 35μg to bring the chromium intake into a consensus with the official Recommended Dietary Allowance.[111][112] A table of the old and new adult daily values in the United States is provided at Reference Daily Intake.
After evaluation of research on the potential nutritional value of chromium, the European Food Safety Authority concluded that there was no evidence of benefit by dietary chromium in healthy people, thereby declining to establish recommendations in Europe for dietary intake of chromium.[15]
Food sources
Food composition databases such as those maintained by the U.S. Department of Agriculture do not contain information on the chromium content of foods.[113] A wide variety of animal and vegetable foods contain chromium.[13][108] Content per serving is influenced by the chromium content of the soil in which the plants are grown, by foodstuffs fed to animals, and by processing methods, as chromium is leached into foods if processed or cooked in stainless steel equipment.[114] One diet analysis study conducted in Mexico reported an average daily chromium intake of 30 micrograms.[115] An estimated 31% of adults in the United States consume multi-vitamin/mineral dietary supplements,[116] which often contain 25 to 60 micrograms of chromium.
Supplementation
Chromium is an ingredient in total parenteral nutrition (TPN), because deficiency can occur after months of intravenous feeding with chromium-free TPN.[117] It is also added to nutritional products for preterm infants.[118] Although the mechanism of action 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.[116] Chemical compounds used in dietary supplements include chromium chloride, chromium citrate, chromium(III) picolinate, chromium(III) polynicotinate, and other chemical compositions.[13] The benefit of supplements has not been proven.[13][119]
Initiation of research on glucose
The notion of chromium as a potential regulator of glucose metabolism began in the 1950s when scientists performed a series of experiments controlling the diet of rats.[120] The experimenters subjected the rats to a chromium deficient diet, and witnessed an inability to respond effectively to increased levels of blood glucose. A chromium-rich Brewer's yeast was provided in the diet, enabling the rats to effectively metabolize glucose, and so giving evidence that chromium may have a role in glucose management.[120]
Approved and disapproved health claims
In 2005, the U.S. Food and Drug Administration had approved a qualified health claim for chromium picolinate with a requirement for 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 type2 diabetes. FDA concludes, however, that the existence of such a relationship between chromium picolinate and either insulin resistance or type2 diabetes is highly uncertain."
In other parts of the petition, the FDA rejected claims for chromium picolinate and cardiovascular disease, retinopathy or kidney disease caused by abnormally high blood sugar levels.[121] As of March 2024, this ruling on chromium remains in effect.[122]
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.[123] The European Food Safety Authority 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.[124]
However, in a 2014 reassessment of studies to determine whether a Dietary Reference Intake value could be established for chromium, EFSA stated:[15]
"The Panel concludes that no Average Requirement and no Population Reference Intake for chromium for the performance of physiological functions can be defined." and
"The Panel considered that there is no evidence of beneficial effects associated with chromium intake in healthy subjects. The Panel concludes that the setting of an Adequate Intake for chromium is also not appropriate."
Diabetes
Given the evidence for chromium deficiency causing problems with glucose management in the context of intravenous nutrition products formulated without chromium,[117] research interest turned to whether chromium supplementation would benefit people who have type2 diabetes but are not chromium deficient. Looking at the results from four meta-analyses, one reported a statistically significant decrease in fasting plasma glucose levels and a non-significant trend in lower hemoglobin A1C.[125] A second reported the same,[126] a third reported significant decreases for both measures,[127] while a fourth reported no benefit for either.[128] 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 fasting blood glucose 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.[129]
Body weight
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 common supplement ingredient, reported a statistically significant −1.1kg (2.4lb) weight loss in trials longer than 12 weeks.[130] The other included all chromium compounds and reported a statistically significant −0.50kg (1.1lb) weight change.[131] 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.[130][131] The European Food Safety Authority reviewed the literature and concluded that there was insufficient evidence to support a claim.[15]
Sports
Chromium is promoted as a sports performance dietary supplement, based on the theory that it potentiates insulin activity, with anticipated results of increased muscle mass, and faster recovery of glycogen storage during post-exercise recovery.[119][132][133] A review of clinical trials reported that chromium supplementation did not improve exercise performance or increase muscle strength.[134] 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.[135]
Fresh-water fish
Irrigation water standards for chromium are 0.1mg/L, but some rivers in Bangladesh are more than five times that amount. The standard for fish for human consumption is less than 1mg/kg, but many tested samples were more than five times that amount.[136] 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.[137]
Acute and chronic exposure to chromium(VI) affects 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.[137]
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 500μg of chromium in the form of chromium chloride or other supplement types, per kilogram of food (dry weight), increased weight gain. At 2,000μg/kg the weight gain was no better than with the zero chromium diet, and there were increased DNA strand breaks.[138]
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.[139] Because of the specific transport mechanisms, only limited amounts of chromium(III) enter the cells. Acute oral toxicity ranges between 50 and 150mg/kg.[140] A 2008 review suggested that moderate uptake of chromium(III) through dietary supplements poses no genetic-toxic risk.[141] 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 1mg/m3. The National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 0.5mg/m3, time-weighted average. The IDLH (immediately dangerous to life and health) value is 250mg/m3.[142]
Chromium(VI) toxicity
The acute oraltoxicity for chromium(VI) ranges between 1.5 and 3.3mg/kg.[140] 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.[143]
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.[144][145] 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.[146][147]
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.[148][149]
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.[151]
The more toxic hexavalent chromium form can be reduced to the less soluble trivalent oxidation state in soils by organic matter, ferrous iron, sulfides, and other reducing agents, with the rates of such reduction being faster under more acidic conditions than under more alkaline ones. In contrast, trivalent chromium can be oxidized to hexavalent chromium in soils by manganese oxides, such as Mn(III) and Mn(IV) compounds. Since the solubility and toxicity of chromium (VI) are greater that those of chromium (III), the oxidation-reduction conversions between the two oxidation states have implications for movement and bioavailability of chromium in soils, groundwater, and plants.[152]
Notes
↑ The melting/boiling point of transition metals are usually higher compared to the alkali metals, alkaline earth metals, and nonmetals, which is why the range of elements compared to chromium differed between comparisons
↑ Most common oxidation states of chromium are in bold. The right column lists a representative compound for each oxidation state.
↑ Any color of corundum (disregarding red) is known as a sapphire. If the corundum is red, then it is a ruby. Sapphires are not required to be blue corundum crystals, as sapphires can be other colors such as yellow and purple
↑ When Cr3+ replaces Al3+ in corundum (aluminium oxide, Al2O3), pink sapphire or ruby is formed, depending on the amount of chromium.
Related Research Articles
Chromic acid is jargon for a solution formed by the addition of sulfuric acid to aqueous solutions of dichromate. It consists at least in part of chromium trioxide.
Chromate salts contain the chromate anion, CrO2− 4. Dichromate salts contain the dichromate anion, Cr 2O2− 7. They are oxyanions of chromium in the +6 oxidation state and are moderately strong oxidizing agents. In an aqueous solution, chromate and dichromate ions can be interconvertible.
Chromite is a crystalline mineral composed primarily of iron(II) oxide and chromium(III) oxide compounds. It can be represented by the chemical formula of FeCr2O4. It is an oxide mineral belonging to the spinel group. The element magnesium can substitute for iron in variable amounts as it forms a solid solution with magnesiochromite (MgCr2O4). Substitution of the element aluminium can also occur, leading to hercynite (FeAl2O4). Chromite today is mined particularly to make stainless steel through the production of ferrochrome (FeCr), which is an iron-chromium alloy.
Potassium dichromate, K2Cr2O7, is a common inorganic chemical reagent, most commonly used as an oxidizing agent in various laboratory and industrial applications. As with all hexavalent chromium compounds, it is acutely and chronically harmful to health. It is a crystalline ionic solid with a very bright, red-orange color. The salt is popular in laboratories because it is not deliquescent, in contrast to the more industrially relevant salt sodium dichromate.
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 and bright orange when wet. The substance dissolves in water accompanied by hydrolysis. Millions of kilograms are produced annually, mainly for electroplating. Chromium trioxide is a powerful oxidiser, a mutagen, and a carcinogen.
Hexavalent chromium (chromium(VI), Cr(VI), chromium 6) is any chemical compound that contains the element chromium in the +6 oxidation state (thus hexavalent). It has been identified as carcinogenic, which is of concern since approximately 136,000 tonnes (150,000 tons) of hexavalent chromium were produced in 1985. Hexavalent chromium compounds can be carcinogens (IARC Group 1), especially if airborne and inhaled where they can cause lung cancer.
Chromium(III) oxide is an inorganic compound with the formula Cr 2O 3. 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(III) picolinate is a chemical compound with the formula Cr(C5H4N )3, commonly abbreviated as CrPic3. It is a bright-red coordination compound derived from chromium(III) and picolinic acid.
Chromium deficiency is described as the consequence of an insufficient dietary intake of the mineral chromium. Chromium was first proposed as an essential element for normal glucose metabolism in 1959, but its biological function has not been identified. Cases of deficiency were described in people who received all of their nutrition intravenously for long periods of time.
Sodium dichromate is the inorganic compound with the formula Na2Cr2O7. However, the salt is usually handled as its dihydrate Na2Cr2O7·2H2O. Virtually all chromium ore is processed via conversion to sodium dichromate and virtually all compounds and materials based on chromium are prepared from this salt. In terms of reactivity and appearance, sodium dichromate and potassium dichromate are very similar. The sodium salt is, however, around twenty times more soluble in water than the potassium salt (49 g/L at 0 °C) and its equivalent weight is also lower, which is often desirable.
Chromate conversion coating or alodine coating is a type of conversion coating used to passivate steel, aluminium, zinc, cadmium, copper, silver, titanium, magnesium, and tin alloys. The coating serves as a corrosion inhibitor, as a primer to improve the adherence of paints and adhesives, as a decorative finish, or to preserve electrical conductivity. It also provides some resistance to abrasion and light chemical attack on soft metals.
Chromyl chloride is an inorganic compound with the formula CrO2Cl2. It is a reddish brown compound that is a volatile liquid at room temperature, which is unusual for transition metal compounds. It is the dichloride of chromic acid.
Chromium compounds are compounds containing the element chromium (Cr). Chromium is a member of group 6 of the transition metals. The +3 and +6 states occur most commonly within chromium compounds, followed by +2; charges of +1, +4 and +5 for chromium are rare, but do nevertheless occasionally exist.
Chromium(III) sulfate usually refers to the inorganic compounds with the formula Cr2(SO4)3.x(H2O), where x can range from 0 to 18. Additionally, ill-defined but commercially important "basic chromium sulfates" are known. These salts are usually either violet or green solids that are soluble in water. It is commonly used in tanning leather.
Sodium chromate is the inorganic compound with the formula Na2CrO4. It exists as a yellow hygroscopic solid, which can form tetra-, hexa-, and decahydrates. It is an intermediate in the extraction of chromium from its ores.
Chromate or chromat, and their derived terms, may refer to:
Chromium toxicity refers to any poisonous toxic effect in an organism or cell that results from exposure to specific forms of chromium—especially hexavalent chromium. Hexavalent chromium and its compounds are toxic when inhaled or ingested. Trivalent chromium is a trace mineral that is essential to human nutrition. There is a hypothetical risk of genotoxicity in humans if large amounts of trivalent chromium were somehow able to enter living cells, but normal metabolism and cell function prevent this.
Chromium(VI) oxide peroxide is the name given to a collection of chromium coordination complexes. They have the formula CrO(O2)2L where L is a ligand. These species are dark blue and often labile. They all feature oxo ligand and two peroxo ligands, with the remaining coordination sites occupied by water, hydroxide, ether, or other Lewis bases.
The Jones oxidation is an organic reaction for the oxidation of primary and secondary alcohols to carboxylic acids and ketones, respectively. It is named after its discoverer, Sir Ewart Jones. The reaction was an early method for the oxidation of alcohols. Its use has subsided because milder, more selective reagents have been developed, e.g. Collins reagent.
Chromium(III) phosphate describes inorganic compounds with the chemical formula CrPO4·(H2O)n, where n = 0, 4, or 6. All are deeply colored solids. Anhydrous CrPO4 is green. The hexahydrate CrPO4·6H2O is violet.
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