Main isotopes			Decay
	abundance	half-life (t_1/2)	mode	product
⁵⁶Co	synth	77.236 d	β⁺	⁵⁶Fe
⁵⁷Co	synth	271.811 d	ε	⁵⁷Fe
⁵⁸Co	synth	70.844 d	β⁺	⁵⁸Fe
⁵⁹Co	100%	stable
⁶⁰Co	trace	5.2714 y	β⁻100%	⁶⁰Ni

Cobalt is a chemical element with the symbol Co and atomic number 27. As with nickel, cobalt is found in the Earth's crust only in a chemically combined form, save for small deposits found in alloys of natural meteoric iron. The free element, produced by reductive smelting, is a hard, lustrous, silver metal.

Cobalt-based blue pigments (cobalt blue) have been used since ancient times for jewelry and paints, and to impart a distinctive blue tint to glass, but the color was for a long time thought to be due to the known metal bismuth. Miners had long used the name kobold ore (German for goblin ore) for some of the blue-pigment-producing minerals; they were so named, because they were poor in known metals, and gave off poisonous arsenic-containing fumes when smelted. In 1735, such ores were found to be reducible to a new metal (the first discovered since ancient times), and this was ultimately named for the kobold.

Today, some cobalt is produced specifically from one of a number of metallic-lustered ores, such as cobaltite (CoAsS). The element is, however, more usually produced as a by-product of copper and nickel mining. The Copperbelt in the Democratic Republic of the Congo (DRC) and Zambia yields most of the global cobalt production. World production in 2016 was 116,000 tonnes (114,000 long tons; 128,000 short tons) (according to Natural Resources Canada), and the DRC alone accounted for more than 50%.

Cobalt is primarily used in lithium-ion batteries, and in the manufacture of magnetic, wear-resistant and high-strength alloys. The compounds cobalt silicate and cobalt(II) aluminate (CoAl₂O₄, cobalt blue) give a distinctive deep blue color to glass, ceramics, inks, paints and varnishes. Cobalt occurs naturally as only one stable isotope, cobalt-59. Cobalt-60 is a commercially important radioisotope, used as a radioactive tracer and for the production of high-energy gamma rays.

Cobalt is the active center of a group of coenzymes called cobalamins. Vitamin B₁₂, the best-known example of the type, is an essential vitamin for all animals. Cobalt in inorganic form is also a micronutrient for bacteria, algae, and fungi.

Characteristics

A block of electrolytically refined cobalt (99.9% purity) cut from a large plate

Cobalt is a ferromagnetic metal with a specific gravity of 8.9. The Curie temperature is 1,115 °C (2,039 °F) and the magnetic moment is 1.6–1.7 Bohr magnetons per atom. Cobalt has a relative permeability two-thirds that of iron.Metallic cobalt occurs as two crystallographic structures: hcp and fcc. The ideal transition temperature between the hcp and fcc structures is 450 °C (842 °F), but in practice the energy difference between them is so small that random intergrowth of the two is common.

Cobalt is a weakly reducing metal that is protected from oxidation by a passivating oxide film. It is attacked by halogens and sulfur. Heating in oxygen produces Co₃O₄ which loses oxygen at 900 °C (1,650 °F) to give the monoxide CoO. The metal reacts with fluorine (F₂) at 520 K to give CoF₃; with chlorine (Cl₂), bromine (Br₂) and iodine (I₂), producing equivalent binary halides. It does not react with hydrogen gas (H₂) or nitrogen gas (N₂) even when heated, but it does react with boron, carbon, phosphorus, arsenic and sulfur. At ordinary temperatures, it reacts slowly with mineral acids, and very slowly with moist, but not dry, air.

Compounds

Common oxidation states of cobalt include +2 and +3, although compounds with oxidation states ranging from −3 to +5 are also known. A common oxidation state for simple compounds is +2 (cobalt(II)). These salts form the pink-colored metal aquo complex [Co(H
₂O)
₆]²⁺
in water. Addition of chloride gives the intensely blue [CoCl
₄]²⁻
. In a borax bead flame test, cobalt shows deep blue in both oxidizing and reducing flames.

Oxygen and chalcogen compounds

Several oxides of cobalt are known. Green cobalt(II) oxide (CoO) has rocksalt structure. It is readily oxidized with water and oxygen to brown cobalt(III) hydroxide (Co(OH)₃). At temperatures of 600–700 °C, CoO oxidizes to the blue cobalt(II,III) oxide (Co₃O₄), which has a spinel structure. Black cobalt(III) oxide (Co₂O₃) is also known. Cobalt oxides are antiferromagnetic at low temperature: CoO (Néel temperature 291 K) and Co₃O₄ (Néel temperature: 40 K), which is analogous to magnetite (Fe₃O₄), with a mixture of +2 and +3 oxidation states.

The principal chalcogenides of cobalt include the black cobalt(II) sulfides, CoS₂, which adopts a pyrite-like structure, and cobalt(III) sulfide (Co₂S₃).

Halides

Cobalt(II) chloride hexahydrate

Four dihalides of cobalt(II) are known: cobalt(II) fluoride (CoF₂, pink), cobalt(II) chloride (CoCl₂, blue), cobalt(II) bromide (CoBr₂, green), cobalt(II) iodide (CoI₂, blue-black). These halides exist in anhydrous and hydrated forms. Whereas the anhydrous dichloride is blue, the hydrate is red.

The reduction potential for the reaction Co³⁺
+ e⁻ → Co²⁺
is +1.92 V, beyond that for chlorine to chloride, +1.36 V. Consequently, cobalt(III) chloride would spontaneously reduce to cobalt(II) chloride and chlorine. Because the reduction potential for fluorine to fluoride is so high, +2.87 V, cobalt(III) fluoride is one of the few simple stable cobalt(III) compounds. Cobalt(III) fluoride, which is used in some fluorination reactions, reacts vigorously with water.

Coordination compounds

As for all metals, molecular compounds and polyatomic ions of cobalt are classified as coordination complexes, that is, molecules or ions that contain cobalt linked to one or more ligands. These can be combinations of a potentially infinite variety of molecules and ions, such as:

water H
₂O, as in the cation hexaaquocobalt(II) [Co(H
₂O)
₆]²⁺
. This pink-colored complex is the predominant cation in solid cobalt sulfate CoSO
₄·(H
₂O)_x, with x = 6 or 7, as well as in water solutions thereof.
ammonia NH
₃, as in cis-diaquotetraamminecobalt(III) [Co(NH
₃)
₄(H
₂O)
₂]³⁺
, in hexol [Co(Co(NH
₃)
₄(HO)
₂)
₃]⁶⁻
, in [Co(NO
₂)
₄(NH
₃)
₂]⁻
(the anion of Erdmann's salt), and in [Co(NH
₃)
₅(CO
₃)]⁻
.
carbonate [CO
₃]²⁻
, as in the green triscarbonatocobaltate(III) [Co(CO
₃)
₃]³⁻
anion.
nitrite [NO
₂]⁻
as in [Co(NO
₂)
₄(NH
₃)
₂]⁻
.
hydroxide [HO]⁻
, as in hexol.
chloride [Cl]⁻
, as in tetrachloridocobaltate(II) CoCl
₄]²⁻
.
bicarbonate [HCO
₃]⁻
, as in [Co(CO
₃)
₂(HCO
₃)(H
₂O)]³⁻
.
oxalate [C
₂O
₄]²⁻
, as in trisoxalatocobaltate(III) [Co(C
₂O
₄)³⁻
_3].

These attached groups affect the stability of oxidation states of the cobalt atoms, according to general principles of electronegativity and of the hardness–softness. For example, Co³⁺ complexes tend to have ammine ligands. Because phosphorus is softer than nitrogen, phosphine ligands tend to feature the softer Co²⁺ and Co⁺, an example being tris(triphenylphosphine)cobalt(I) chloride (P(C
₆H
₅)
₃)
₃CoCl). The more electronegative (and harder) oxide and fluoride can stabilize Co⁴⁺ and Co⁵⁺ derivatives, e.g. caesium hexafluorocobaltate(IV) (Cs₂CoF₆) and potassium percobaltate (K₃CoO₄).

Alfred Werner, a Nobel-prize winning pioneer in coordination chemistry, worked with compounds of empirical formula [Co(NH
₃)
₆]³⁺
. One of the isomers determined was cobalt(III) hexammine chloride. This coordination complex, a typical Werner-type complex, consists of a central cobalt atom coordinated by six ammine orthogonal ligands and three chloride counteranions. Using chelating ethylenediamine ligands in place of ammonia gives tris(ethylenediamine)cobalt(III) ([Co(en)
₃]³⁺
), which was one of the first coordination complexes to be resolved into optical isomers. The complex exists in the right- and left-handed forms of a "three-bladed propeller". This complex was first isolated by Werner as yellow-gold needle-like crystals.

Organometallic compounds

Structure of tetrakis(1-norbornyl)cobalt(IV)

Cobaltocene is a structural analog to ferrocene, with cobalt in place of iron. Cobaltocene is much more sensitive to oxidation than ferrocene. Cobalt carbonyl (Co₂(CO)₈) is a catalyst in carbonylation and hydrosilylation reactions. Vitamin B₁₂ (see below) is an organometallic compound found in nature and is the only vitamin that contains a metal atom. An example of an alkylcobalt complex in the otherwise uncommon +4 oxidation state of cobalt is the homoleptic complex tetrakis(1-norbornyl)cobalt(IV) (Co(1-norb)₄), a transition metal-alkyl complex that is notable for its resistance to β-hydrogen elimination, in accord with Bredt's rule. The cobalt(III) and cobalt(V) complexes [Li(THF)
₄]⁺
[Co(1-norb)
₄]⁻
and [Co(1-norb)
₄]⁺
[BF
₄]⁻
are also known.

Isotopes

⁵⁹Co is the only stable cobalt isotope and the only isotope that exists naturally on Earth. Twenty-two radioisotopes have been characterized: the most stable, ⁶⁰Co, has a half-life of 5.2714 years; ⁵⁷Co has a half-life of 271.8 days; ⁵⁶Co has a half-life of 77.27 days; and ⁵⁸Co has a half-life of 70.86 days. All the other radioactive isotopes of cobalt have half-lives shorter than 18 hours, and in most cases shorter than 1 second. This element also has 4 meta states, all of which have half-lives shorter than 15 minutes.

The isotopes of cobalt range in atomic weight from 50 u (⁵⁰Co) to 73 u (⁷³Co). The primary decay mode for isotopes with atomic mass unit values less than that of the only stable isotope, ⁵⁹Co, is electron capture and the primary mode of decay in isotopes with atomic mass greater than 59 atomic mass units is beta decay. The primary decay products below ⁵⁹Co are element 26 (iron) isotopes; above that the decay products are element 28 (nickel) isotopes.

History

Early Chinese blue and white porcelain, manufactured c. 1335

Cobalt compounds have been used for centuries to impart a rich blue color to glass, glazes, and ceramics. Cobalt has been detected in Egyptian sculpture, Persian jewelry from the third millennium BC, in the ruins of Pompeii, destroyed in 79 AD, and in China, dating from the Tang dynasty (618–907 AD) and the Ming dynasty (1368–1644 AD).

Cobalt has been used to color glass since the Bronze Age. The excavation of the Uluburun shipwreck yielded an ingot of blue glass, cast during the 14th century BC. Blue glass from Egypt was either colored with copper, iron, or cobalt. The oldest cobalt-colored glass is from the eighteenth dynasty of Egypt (1550–1292 BC). The source for the cobalt the Egyptians used is not known.

The word cobalt is derived from the German kobalt, from kobold meaning "goblin", a superstitious term used for the ore of cobalt by miners. The first attempts to smelt those ores for copper or silver failed, yielding simply powder (cobalt(II) oxide) instead. Because the primary ores of cobalt always contain arsenic, smelting the ore oxidized the arsenic into the highly toxic and volatile arsenic oxide, adding to the notoriety of the ore.Paracelsus, Georgius Agricola, and Basil Valentine all referred to such silicates as "cobalt".

Swedish chemist Georg Brandt (1694–1768) is credited with discovering cobalt c. 1735, showing it to be a previously unknown element, distinct from bismuth and other traditional metals. Brandt called it a new "semi-metal". He showed that compounds of cobalt metal were the source of the blue color in glass, which previously had been attributed to the bismuth found with cobalt. Cobalt became the first metal to be discovered since the pre-historical period. All other known metals (iron, copper, silver, gold, zinc, mercury, tin, lead and bismuth) had no recorded discoverers.

During the 19th century, a significant part of the world's production of cobalt blue (a pigment made with cobalt compounds and alumina) and smalt (cobalt glass powdered for use for pigment purposes in ceramics and painting) was carried out at the Norwegian Blaafarveværket. The first mines for the production of smalt in the 16th century were located in Norway, Sweden, Saxony and Hungary. With the discovery of cobalt ore in New Caledonia in 1864, the mining of cobalt in Europe declined. With the discovery of ore deposits in Ontario, Canada in 1904 and the discovery of even larger deposits in the Katanga Province in the Congo in 1914, the mining operations shifted again. When the Shaba conflict started in 1978, the copper mines of Katanga Province nearly stopped production. The impact on the world cobalt economy from this conflict was smaller than expected: cobalt is a rare metal, the pigment is highly toxic, and the industry had already established effective ways for recycling cobalt materials. In some cases, industry was able to change to cobalt-free alternatives.

In 1938, John Livingood and Glenn T. Seaborg discovered the radioisotope cobalt-60. This isotope was famously used at Columbia University in the 1950s to establish parity violation in radioactive beta decay.

After World War II, the US wanted to guarantee the supply of cobalt ore for military uses (as the Germans had been doing) and prospected for cobalt within the U.S. border. An adequate supply of the ore was found in Idaho near Blackbird canyon in the side of a mountain. The firm Calera Mining Company started production at the site.

It has been argued that cobalt will be one of the main objects of geopolitical competition in a world running on renewable energy and dependent on batteries, but this perspective has also been criticised for underestimating the power of economic incentives for expanded production.

Occurrence

The stable form of cobalt is produced in supernovae through the r-process. It comprises 0.0029% of the Earth's crust. Free cobalt (the native metal) is not found on Earth because of the oxygen in the atmosphere and the chlorine in the ocean. Both are abundant enough in the upper layers of the Earth's crust to prevent native metal cobalt from forming. Except as recently delivered in meteoric iron, pure cobalt in native metal form is unknown on Earth. The element has a medium abundance but natural compounds of cobalt are numerous and small amounts of cobalt compounds are found in most rocks, soils, plants, and animals.

In nature, cobalt is frequently associated with nickel. Both are characteristic components of meteoric iron, though cobalt is much less abundant in iron meteorites than nickel. As with nickel, cobalt in meteoric iron alloys may have been well enough protected from oxygen and moisture to remain as the free (but alloyed) metal, though neither element is seen in that form in the ancient terrestrial crust.

Cobalt in compound form occurs in copper and nickel minerals. It is the major metallic component that combines with sulfur and arsenic in the sulfidic cobaltite (CoAsS), safflorite (CoAs₂), glaucodot ((Co,Fe)AsS), and skutterudite (CoAs₃) minerals. The mineral cattierite is similar to pyrite and occurs together with vaesite in the copper deposits of Katanga Province. When it reaches the atmosphere, weathering occurs; the sulfide minerals oxidize and form pink erythrite ("cobalt glance": Co₃(AsO₄)₂·8H₂O) and spherocobaltite (CoCO₃).

Cobalt is also a constituent of tobacco smoke. The tobacco plant readily absorbs and accumulates heavy metals like cobalt from the surrounding soil in its leaves. These are subsequently inhaled during tobacco smoking.

In the ocean

Cobalt is a trace metal involved in photosynthesis and nitrogen fixation detected in most ocean basins and is a limiting micronutrient for phytoplankton and cyanobacteria. The Co-containing complex cobalamin is only synthesized by cyanobacteria and a few archaea, so dissolved cobalt concentrations are low in the upper ocean. Like Mn and Fe, Co has a hybrid profile of biological uptake by phytoplankton via photosynthesis in the upper ocean and scavenging in the deep ocean, although most scavenging is limited by complex organic ligands. Co is recycled in the ocean by decaying organic matter that sinks below the upper ocean, although most is scavenged by oxidizing bacteria.

Sources of cobalt for many ocean bodies include rivers and terrestrial runoff with some input from hydrothermal vents. In the deep ocean, cobalt sources are found lying on top of seamounts (which can be large or small) where ocean currents sweep the ocean floor to clear sediment over the span of millions of years allowing them to form as ferromanganese crusts. Although limited mapping of the seafloor has been done, preliminary investigation indicates that there is a large amount of these cobalt-rich crusts located in the Clarion Clipperton Zone, an area garnering increasing interest for deep sea mining ventures due to the mineral-rich environment within its domain. Anthropogenic input contributes as a non-natural source but in very low amounts. Dissolved cobalt (dCo) concentrations across oceans are controlled primarily by reservoirs where dissolved oxygen concentrations are low. The complex biochemical cycling of cobalt in the ocean is still not fully understood, but patterns of higher concentrations have been found in areas of low oxygen such as the Oxygen Minimum Zone (OMZ) in the Southern Atlantic Ocean.

Cobalt is considered toxic for marine environments at high concentrations. Safe concentrations fall around 18 μg/L in marine waters for plankton such as diatoms.

Production

Cobalt ore

Cobalt mine production (2022) and reserves in tonnes according to USGS
Country	Production	Reserves
DR Congo	130,000	4,000,000
Indonesia	10,000	600,000
Russia	8,900	250,000
Australia	5,900	1,500,000
Canada	3,900	220,000
Cuba	3,800	500,000
Philippines	3,800	260,000
Madagascar	3,000	100,000
Papua New Guinea	3,000	47,000
Turkey	2,700	36,000
Morocco	2,300	13,000
China	2,200	140,000
United States	800	69,000
Other countries	5,200	610,000
World total	190,000	8,300,000

The main ores of cobalt are cobaltite, erythrite, glaucodot and skutterudite (see above), but most cobalt is obtained by reducing the cobalt by-products of nickel and copper mining and smelting.

Since cobalt is generally produced as a by-product, the supply of cobalt depends to a great extent on the economic feasibility of copper and nickel mining in a given market. Demand for cobalt was projected to grow 6% in 2017.

Primary cobalt deposits are rare, such as those occurring in hydrothermal deposits, associated with ultramafic rocks, typified by the Bou-Azzer district of Morocco. At such locations, cobalt ores are mined exclusively, albeit at a lower concentration, and thus require more downstream processing for cobalt extraction.

Several methods exist to separate cobalt from copper and nickel, depending on the concentration of cobalt and the exact composition of the used ore. One method is froth flotation, in which surfactants bind to ore components, leading to an enrichment of cobalt ores. Subsequent roasting converts the ores to cobalt sulfate, and the copper and the iron are oxidized to the oxide. Leaching with water extracts the sulfate together with the arsenates. The residues are further leached with sulfuric acid, yielding a solution of copper sulfate. Cobalt can also be leached from the slag of copper smelting.

The products of the above-mentioned processes are transformed into the cobalt oxide (Co₃O₄). This oxide is reduced to metal by the aluminothermic reaction or reduction with carbon in a blast furnace.

World production trend

Extraction

The United States Geological Survey estimates world reserves of cobalt at 7,100,000 metric tons. The Democratic Republic of the Congo (DRC) currently produces 63% of the world's cobalt. This market share may reach 73% by 2025 if planned expansions by mining producers like Glencore Plc take place as expected. Bloomberg New Energy Finance has estimated that by 2030, global demand for cobalt could be 47 times more than it was in 2017.

Changes that Congo made to mining laws in 2002 attracted new investments in Congolese copper and cobalt projects. Glencore's Mutanda Mine shipped 24,500 tons of cobalt in 2016, 40% of Congo DRC's output and nearly a quarter of global production. After oversupply, Glencore closed Mutanda for two years in late 2019. Glencore's Katanga Mining project is resuming as well and should produce 300,000 tons of copper and 20,000 tons of cobalt by 2019, according to Glencore.

Democratic Republic of the Congo

In 2005, the top producer of cobalt was the copper deposits in the Democratic Republic of the Congo's Katanga Province. Formerly Shaba province, the area had almost 40% of global reserves, reported the British Geological Survey in 2009.

Artisanal mining supplied 17% to 40% of the DRC production. Some 100,000 cobalt miners in Congo DRC use hand tools to dig hundreds of feet, with little planning and fewer safety measures, say workers and government and NGO officials, as well as The Washington Post reporters' observations on visits to isolated mines. The lack of safety precautions frequently causes injuries or death. Mining pollutes the vicinity and exposes local wildlife and indigenous communities to toxic metals thought to cause birth defects and breathing difficulties, according to health officials.

Human rights activists have alleged, and investigative journalism reported confirmation, that child labor is used in mining cobalt from African artisanal mines. This revelation prompted cell phone maker Apple Inc., on March 3, 2017, to stop buying ore from suppliers such as Zhejiang Huayou Cobalt who source from artisanal mines in the DRC, and begin using only suppliers that are verified to meet its workplace standards.

There is a push globally by the EU and major car manufacturers (OEM) for global production of cobalt to be sourced and produced sustainably, responsibly and traceability of the supply chain. Mining companies are adopting and practising ESG initiatives in line with OECD Guidance and putting in place evidence of zero to low carbon footprint activities in the supply chain production of Lithium-ion batteries. These initiatives are already taking place with major mining companies, Artisanal and Small-Scale Mining companies (ASM). Car manufacturers and battery manufacturer supply chains Tesla, VW, BMW, BASF, Glencore are participating in several initiatives, such as the Responsible Cobalt Initiative and Cobalt for Development study. In 2018 BMW Group in partnership with BASF, Samsung SDI and Samsung Electronics have launched a pilot project in the DRC over one pilot mine, to improve conditions and address challenges for artisanal miners and the surrounding communities.

The political and ethnic dynamics of the region have in the past caused outbreaks of violence and years of armed conflict and displaced populations. This instability affected the price of cobalt and also created perverse incentives for the combatants in the First and Second Congo Wars to prolong the fighting, since access to diamond mines and other valuable resources helped to finance their military goals—which frequently amounted to genocide—and also enriched the fighters themselves. While DR Congo has in the 2010s not recently been invaded by neighboring military forces, some of the richest mineral deposits adjoin areas where Tutsis and Hutus still frequently clash, unrest continues although on a smaller scale and refugees still flee outbreaks of violence.

Cobalt extracted from small Congolese artisanal mining endeavors in 2007 supplied a single Chinese company, Congo DongFang International Mining. A subsidiary of Zhejiang Huayou Cobalt, one of the world's largest cobalt producers, Congo DongFang supplied cobalt to some of the world's largest battery manufacturers, who produced batteries for ubiquitous products like the Apple iPhones. Because of accused labour violations and environmental concerns, LG Chem subsequently audited Congo DongFang in accordance with OECD guidelines. LG Chem, which also produces battery materials for car companies, imposed a code of conduct on all suppliers that it inspects.

The Mukondo Mountain project, operated by the Central African Mining and Exploration Company (CAMEC) in Katanga Province, may be the richest cobalt reserve in the world. It produced an estimated one-third of the total global cobalt production in 2008. In July 2009, CAMEC announced a long-term agreement to deliver its entire annual production of cobalt concentrate from Mukondo Mountain to Zhejiang Galico Cobalt & Nickel Materials of China.

In February 2018, global asset management firm AllianceBernstein defined the DRC as economically "the Saudi Arabia of the electric vehicle age", due to its cobalt resources, as essential to the lithium-ion batteries that drive electric vehicles.

On March 9, 2018, President Joseph Kabila updated the 2002 mining code, increasing royalty charges and declaring cobalt and coltan "strategic metals".

The 2002 mining code was effectively updated on December 4, 2018.

In December 2019, International Rights Advocates, a human rights NGO, filed a landmark lawsuit against Apple, Tesla, Dell, Microsoft and Google company Alphabet for "knowingly benefiting from and aiding and abetting the cruel and brutal use of young children" in mining cobalt. The companies in question denied their involvement in child labour.

Canada

In 2017, some exploration companies were planning to survey old silver and cobalt mines in the area of Cobalt, Ontario, where significant deposits are believed to lie.

Cuba

Canada's Sherritt International processes cobalt ores in nickel deposits from the Moa mines in Cuba, and the island has several others mines in Mayari, Camaguey, and Pinar del Rio. Continued investments by Sherritt International in Cuban nickel and cobalt production while acquiring mining rights for 17–20 years made the communist country third for cobalt reserves in 2019, before Canada itself.

Indonesia

Starting from smaller amounts in 2021, Indonesia began producing cobalt as a byproduct of nickel production. By 2022, the country had become the world's second-largest cobalt producer, with Benchmark Mineral Intelligence forecasting Indonesian output to make up 20 percent of global production by 2030.

Applications

In 2016, 116,000 tonnes (128,000 short tons) of cobalt was used. Cobalt has been used in the production of high-performance alloys. It is also used in some rechargeable batteries.

Alloys

Cobalt-based superalloys have historically consumed most of the cobalt produced. The temperature stability of these alloys makes them suitable for turbine blades for gas turbines and aircraft jet engines, although nickel-based single-crystal alloys surpass them in performance. Cobalt-based alloys are also corrosion- and wear-resistant, making them, like titanium, useful for making orthopedic implants that don't wear down over time. The development of wear-resistant cobalt alloys started in the first decade of the 20th century with the stellite alloys, containing chromium with varying quantities of tungsten and carbon. Alloys with chromium and tungsten carbides are very hard and wear-resistant. Special cobalt-chromium-molybdenum alloys like Vitallium are used for prosthetic parts (hip and knee replacements). Cobalt alloys are also used for dental prosthetics as a useful substitute for nickel, which may be allergenic. Some high-speed steels also contain cobalt for increased heat and wear resistance. The special alloys of aluminium, nickel, cobalt and iron, known as Alnico, and of samarium and cobalt (samarium-cobalt magnet) are used in permanent magnets. It is also alloyed with 95% platinum for jewelry, yielding an alloy suitable for fine casting, which is also slightly magnetic.

Batteries

Lithium cobalt oxide (LiCoO₂) is widely used in lithium-ion battery cathodes. The material is composed of cobalt oxide layers with the lithium intercalated. During discharge (i.e. when not actively being charged), the lithium is released as lithium ions.Nickel-cadmium (NiCd) and nickel metal hydride (NiMH) batteries also include cobalt to improve the oxidation of nickel in the battery. Transparency Market Research estimated the global lithium-ion battery market at $30 billion in 2015 and predicted an increase to over US$75 billion by 2024.

Although in 2018 most cobalt in batteries was used in a mobile device, a more recent application for cobalt is rechargeable batteries for electric cars. This industry has increased five-fold in its demand for cobalt, which makes it urgent to find new raw materials in more stable areas of the world. Demand is expected to continue or increase as the prevalence of electric vehicles increases. Exploration in 2016–2017 included the area around Cobalt, Ontario, an area where many silver mines ceased operation decades ago. Cobalt for electric vehicles increased 81% from the first half of 2018 to 7,200 tonnes in the first half of 2019, for a battery capacity of 46.3 GWh.

Since child and slave labor have been repeatedly reported in cobalt mining, primarily in the artisanal mines of DR Congo, technology companies seeking an ethical supply chain have faced shortages of this raw material and the price of cobalt metal reached a nine-year high in October 2017, more than US$30 a pound, versus US$10 in late 2015. After oversupply, the price dropped to a more normal $15 in 2019. As a reaction to the issues with artisanal cobalt mining in DR Congo a number of cobalt suppliers and their customers have formed the Fair Cobalt Alliance (FCA) which aims to end the use of child labor and to improve the working conditions of cobalt mining and processing in the DR Congo. Members of FCA include Zhejiang Huayou Cobalt, Sono Motors, the Responsible Cobalt Initiative, Fairphone, Glencore and Tesla, Inc.

Research is being conducted by the European Union into the possibility of eliminating cobalt requirements in lithium-ion battery production. As of August 2020 battery makers have gradually reduced the cathode cobalt content from 1/3 (NMC 111) to 1/5 (NMC 442) to currently 1/10 (NMC 811) and have also introduced the cobalt free lithium iron phosphate cathode into the battery packs of electric cars such as the Tesla Model 3. In September 2020, Tesla outlined their plans to make their own, cobalt-free battery cells.

Lithium iron phosphate batteries officially surpassed ternary cobalt batteries in 2021 with 52% of installed capacity. Analysts estimate that its market share will exceed 60% in 2024.

Catalysts

Several cobalt compounds are oxidation catalysts. Cobalt acetate is used to convert xylene to terephthalic acid, the precursor of the bulk polymer polyethylene terephthalate. Typical catalysts are the cobalt carboxylates (known as cobalt soaps). They are also used in paints, varnishes, and inks as "drying agents" through the oxidation of drying oils. However, their use is being phased out due to toxicity concerns. The same carboxylates are used to improve the adhesion between steel and rubber in steel-belted radial tires. In addition they are used as accelerators in polyester resin systems.

Cobalt-based catalysts are used in reactions involving carbon monoxide. Cobalt is also a catalyst in the Fischer–Tropsch process for the hydrogenation of carbon monoxide into liquid fuels.Hydroformylation of alkenes often uses cobalt octacarbonyl as a catalyst,

The hydrodesulfurization of petroleum uses a catalyst derived from cobalt and molybdenum. This process helps to clean petroleum of sulfur impurities that interfere with the refining of liquid fuels.

Pigments and coloring

Cobalt blue glass

Cobalt-colored glass

Before the 19th century, cobalt was predominantly used as a pigment. It has been used since the Middle Ages to make smalt, a blue-colored glass. Smalt is produced by melting a mixture of roasted mineral smaltite, quartz and potassium carbonate, which yields a dark blue silicate glass, which is finely ground after the production. Smalt was widely used to color glass and as pigment for paintings. In 1780, Sven Rinman discovered cobalt green, and in 1802 Louis Jacques Thénard discovered cobalt blue. Cobalt pigments such as cobalt blue (cobalt aluminate), cerulean blue (cobalt(II) stannate), various hues of cobalt green (a mixture of cobalt(II) oxide and zinc oxide), and cobalt violet (cobalt phosphate) are used as artist's pigments because of their superior chromatic stability.

Radioisotopes

Cobalt-60 (Co-60 or ⁶⁰Co) is useful as a gamma-ray source because it can be produced in predictable amounts with high activity by bombarding cobalt with neutrons. It produces gamma rays with energies of 1.17 and 1.33 MeV.

Cobalt is used in external beam radiotherapy, sterilization of medical supplies and medical waste, radiation treatment of foods for sterilization (cold pasteurization),industrial radiography (e.g. weld integrity radiographs), density measurements (e.g. concrete density measurements), and tank fill height switches. The metal has the unfortunate property of producing a fine dust, causing problems with radiation protection. Cobalt from radiotherapy machines has been a serious hazard when not discarded properly, and one of the worst radiation contamination accidents in North America occurred in 1984, when a discarded radiotherapy unit containing cobalt-60 was mistakenly disassembled in a junkyard in Juarez, Mexico.

Cobalt-60 has a radioactive half-life of 5.27 years. Loss of potency requires periodic replacement of the source in radiotherapy and is one reason why cobalt machines have been largely replaced by linear accelerators in modern radiation therapy.Cobalt-57 (Co-57 or ⁵⁷Co) is a cobalt radioisotope most often used in medical tests, as a radiolabel for vitamin B₁₂ uptake, and for the Schilling test. Cobalt-57 is used as a source in Mössbauer spectroscopy and is one of several possible sources in X-ray fluorescence devices.

Nuclear weapon designs could intentionally incorporate ⁵⁹Co, some of which would be activated in a nuclear explosion to produce ⁶⁰Co. The ⁶⁰Co, dispersed as nuclear fallout, is sometimes called a cobalt bomb.

Other uses

Cobalt is used in electroplating for its attractive appearance, hardness, and resistance to oxidation.
It is also used as a base primer coat for porcelain enamels.

Biological role

Cobalt is essential to the metabolism of all animals. It is a key constituent of cobalamin, also known as vitamin B₁₂, the primary biological reservoir of cobalt as an ultratrace element.Bacteria in the stomachs of ruminant animals convert cobalt salts into vitamin B₁₂, a compound which can only be produced by bacteria or archaea. A minimal presence of cobalt in soils therefore markedly improves the health of grazing animals, and an uptake of 0.20 mg/kg a day is recommended, because they have no other source of vitamin B₁₂.

Proteins based on cobalamin use corrin to hold the cobalt. Coenzyme B₁₂ features a reactive C-Co bond that participates in the reactions. In humans, B₁₂ has two types of alkyl ligand: methyl and adenosyl. MeB₁₂ promotes methyl (−CH₃) group transfers. The adenosyl version of B₁₂ catalyzes rearrangements in which a hydrogen atom is directly transferred between two adjacent atoms with concomitant exchange of the second substituent, X, which may be a carbon atom with substituents, an oxygen atom of an alcohol, or an amine. Methylmalonyl coenzyme A mutase (MUT) converts MMl-CoA to Su-CoA, an important step in the extraction of energy from proteins and fats.

Although far less common than other metalloproteins (e.g. those of zinc and iron), other cobaltoproteins are known besides B₁₂. These proteins include methionine aminopeptidase 2, an enzyme that occurs in humans and other mammals that does not use the corrin ring of B₁₂, but binds cobalt directly. Another non-corrin cobalt enzyme is nitrile hydratase, an enzyme in bacteria that metabolizes nitriles.

Cobalt deficiency

In humans, consumption of cobalt-containing vitamin B₁₂ meets all needs for cobalt. For cattle and sheep, which meet vitamin B₁₂ needs via synthesis by resident bacteria in the rumen, there is a function for inorganic cobalt. In the early 20th century, during the development of farming on the North Island Volcanic Plateau of New Zealand, cattle suffered from what was termed "bush sickness". It was discovered that the volcanic soils lacked the cobalt salts essential for the cattle food chain. The "coast disease" of sheep in the Ninety Mile Desert of the Southeast of South Australia in the 1930s was found to originate in nutritional deficiencies of trace elements cobalt and copper. The cobalt deficiency was overcome by the development of "cobalt bullets", dense pellets of cobalt oxide mixed with clay given orally for lodging in the animal's rumen.

Cobalamin
Cobalt-deficient sheep

Health issues

Cobalt
Hazards
GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H302, H317, H319, H334, H341, H350, H360F, H412
Precautionary statements	P273, P280, P301+P312, P302+P352, P305+P351+P338, P308+P313
NFPA 704 (fire diamond)	2 0 0

The LD₅₀ value for soluble cobalt salts has been estimated to be between 150 and 500 mg/kg. In the US, the Occupational Safety and Health Administration (OSHA) has designated a permissible exposure limit (PEL) in the workplace as a time-weighted average (TWA) of 0.1 mg/m³. The National Institute for Occupational Safety and Health (NIOSH) has set a recommended exposure limit (REL) of 0.05 mg/m³, time-weighted average. The IDLH (immediately dangerous to life and health) value is 20 mg/m³.

However, chronic cobalt ingestion has caused serious health problems at doses far less than the lethal dose. In 1966, the addition of cobalt compounds to stabilize beer foam in Canada led to a peculiar form of toxin-induced cardiomyopathy, which came to be known as beer drinker's cardiomyopathy.

Furthermore, cobalt metal is suspected of causing cancer (i.e., possibly carcinogenic, IARC Group 2B) as per the International Agency for Research on Cancer (IARC) Monographs.

It causes respiratory problems when inhaled. It also causes skin problems when touched; after nickel and chromium, cobalt is a major cause of contact dermatitis.

External links

Wikimedia Commons has media related to Cobalt.

Look up cobalt in Wiktionary, the free dictionary.

Cobalt at The Periodic Table of Videos (University of Nottingham)
Centers for Disease and Prevention – Cobalt
The Cobalt Institute
Responsible Cobalt Institute Archived 2021-03-07 at the Wayback Machine

v t e Cobalt compounds
Cobalt(I)	HCo(CO)₄
Cobalt(II)	CoBr₂ Co(CN)₂ CoCO₃ CoC₂O₄ CoCl₂ Co(ClO₃)₂ CoF₂ Co(HCO₂)₂ CoI₂ Co(NO₃)₂ Co₃(PO₄)₂ Co(OAc)₂ CoO Co(OH)₂ CoS CO(SCN)₂ CoSO₄ CoSe Co₃P₂ CoH₂ Co(C₃H₆O₃)₂ C ₂₄H ₄₈CoO ₄ C ₃₆H ₇₀CoO ₄
Cobalt(0, III)	CoSi CoGe
Cobalt(II, III)	Co₃O₄
Cobalt(III)	CoAs CoCl₃ Co(NO₃)₃ Co₂O₃ CoF₃ Co(OH)₃ LiCoO₂
Cobalt(III,IV)	Na_xCoO₂
Cobalt(IV)	Cs₂CoF₆ CoC₂₈H₄₄
Cobalt(V)	Na₃CoO₄

Cobalt