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Cobalt
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| Cobalt | ||||||||||||||||||||||||||||||||||||
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| Pronunciation | /ˈkoʊbɒlt/ ⓘ[1] | |||||||||||||||||||||||||||||||||||
| Appearance | Hard lustrous bluish gray metal | |||||||||||||||||||||||||||||||||||
| Standard atomic weight Ar°(Co) | ||||||||||||||||||||||||||||||||||||
| Cobalt in the periodic table | ||||||||||||||||||||||||||||||||||||
| Atomic number (Z) | 27 | |||||||||||||||||||||||||||||||||||
| Group | group 9 | |||||||||||||||||||||||||||||||||||
| Period | period 4 | |||||||||||||||||||||||||||||||||||
| Block | d-block | |||||||||||||||||||||||||||||||||||
| Electron configuration | [Ar] 3d7 4s2 | |||||||||||||||||||||||||||||||||||
| Electrons per shell | 2, 8, 15, 2 | |||||||||||||||||||||||||||||||||||
| Physical properties | ||||||||||||||||||||||||||||||||||||
| Phase at STP | solid | |||||||||||||||||||||||||||||||||||
| Melting point | 1768 K (1495 °C, 2723 °F) | |||||||||||||||||||||||||||||||||||
| Boiling point | 3200 K (2927 °C, 5301 °F) | |||||||||||||||||||||||||||||||||||
| Density (at 20° C) | 8.834 g/cm3 [4] | |||||||||||||||||||||||||||||||||||
| when liquid (at m.p.) | 7.75 g/cm3 | |||||||||||||||||||||||||||||||||||
| Heat of fusion | 16.06 kJ/mol | |||||||||||||||||||||||||||||||||||
| Heat of vaporization | 377 kJ/mol | |||||||||||||||||||||||||||||||||||
| Molar heat capacity | 24.81 J/(mol·K) | |||||||||||||||||||||||||||||||||||
Vapor pressure
| ||||||||||||||||||||||||||||||||||||
| Atomic properties | ||||||||||||||||||||||||||||||||||||
| Oxidation states | common: +2, +3 −3,[5] −1,[6] 0,[6] +1,[6] +4,[6] +5[7] | |||||||||||||||||||||||||||||||||||
| Electronegativity | Pauling scale: 1.88 | |||||||||||||||||||||||||||||||||||
| Ionization energies |
| |||||||||||||||||||||||||||||||||||
| Atomic radius | empirical: 125 pm | |||||||||||||||||||||||||||||||||||
| Covalent radius | Low spin: 126±3 pm High spin: 150±7 pm | |||||||||||||||||||||||||||||||||||
| Other properties | ||||||||||||||||||||||||||||||||||||
| Natural occurrence | primordial | |||||||||||||||||||||||||||||||||||
| Crystal structure | hexagonal close-packed (hcp) (hP2) | |||||||||||||||||||||||||||||||||||
| Lattice constants | a = 250.71 pm c = 407.00 pm (at 20 °C)[4] | |||||||||||||||||||||||||||||||||||
| Thermal expansion | 12.9×10−6/K (at 20 °C)[a] | |||||||||||||||||||||||||||||||||||
| Thermal conductivity | 100 W/(m⋅K) | |||||||||||||||||||||||||||||||||||
| Electrical resistivity | 62.4 nΩ⋅m (at 20 °C) | |||||||||||||||||||||||||||||||||||
| Magnetic ordering | Ferromagnetic | |||||||||||||||||||||||||||||||||||
| Young's modulus | 209 GPa | |||||||||||||||||||||||||||||||||||
| Shear modulus | 75 GPa | |||||||||||||||||||||||||||||||||||
| Bulk modulus | 180 GPa | |||||||||||||||||||||||||||||||||||
| Speed of sound thin rod | 4720 m/s (at 20 °C) | |||||||||||||||||||||||||||||||||||
| Poisson ratio | 0.31 | |||||||||||||||||||||||||||||||||||
| Mohs hardness | 5.0 | |||||||||||||||||||||||||||||||||||
| Vickers hardness | 1043 MPa | |||||||||||||||||||||||||||||||||||
| Brinell hardness | 470–3000 MPa | |||||||||||||||||||||||||||||||||||
| CAS Number | 7440-48-4 | |||||||||||||||||||||||||||||||||||
| History | ||||||||||||||||||||||||||||||||||||
| Naming | from the kobelt ore, possibly named after Kobolds | |||||||||||||||||||||||||||||||||||
| Discovery and first isolation | Georg Brandt (1735) | |||||||||||||||||||||||||||||||||||
| Isotopes of cobalt | ||||||||||||||||||||||||||||||||||||
| ||||||||||||||||||||||||||||||||||||
Cobalt is a chemical element; it has 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, somewhat brittle, gray metal.
Cobalt-based blue pigments (cobalt blue) have been used since antiquity for jewelry and paints, and to impart a distinctive blue tint to glass. The color was long thought to be due to the 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.[9] In 1735, such ores were found to be reducible to a new metal (the first discovered since ancient times), which was ultimately named for the kobold.
Today, cobalt is usually produced as a by-product of copper and nickel mining, but sometimes also from one of a number of metallic-lustered ores such as cobaltite (CoAsS). 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%.[10] In 2024, production exceeded 300,000 tons, of which DRC accounted for more than 80%.[11]
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 also used in the petroleum industry as a catalyst when refining crude oil. This is to purge it of sulfur, which is very polluting when burned and causes acid rain.[12]
Cobalt is the active center of a group of coenzymes called cobalamins. [[Vitamin B12|Vitamin B 12]], 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.
The name cobalt derives from a type of ore considered a nuisance by 16th century German silver miners, which in turn may have been named from a spirit or goblin held superstitiously responsible for it; this spirit is considered equitable to the kobold (a household spirit) by some, or, categorized as a gnome (mine spirit) by others.
Characteristics
[edit]
Cobalt is a ferromagnetic metal with a specific gravity of 8.9. The Curie temperature is 1,115 °C (2,039 °F)[13] and the magnetic moment is 1.6–1.7 Bohr magnetons per atom.[14] Cobalt has a relative permeability two-thirds that of iron.[15] 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.[16][17][18]
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.[19] 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.[20] At ordinary temperatures, it reacts slowly with mineral acids, and very slowly with moist, but not dry, air.[citation needed]
Compounds
[edit]
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−
.[7] In a borax bead flame test, cobalt shows deep blue in both oxidizing and reducing flames.[21]
Oxygen and chalcogen compounds
[edit]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.[7] Black cobalt(III) oxide (Co2O3) is also known.[22] 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.[23]
The principal chalcogenides of cobalt are the black cobalt(II) sulfides, CoS2 (pyrite structure), Co2S3 (spinel structure), and CoS (nickel arsenide structure).[7]: 1118
Halides
[edit]
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.[24]
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.[19]
Coordination compounds
[edit]The inventory of complexes is very large. Starting with higher oxidation states, complexes of Co(IV) and Co(V) are rare. Examples are found in caesium hexafluorocobaltate(IV) (Cs2CoF6) and potassium percobaltate (K3CoO4).[19]
Cobalt(III) forms a wide variety of coordination complexes with ammonia and amines, which are called ammine complexes. Examples include [Co(NH3)6]3+, [Co(NH3)5Cl]2+ (chloropentamminecobalt(III)), and cis- and trans-[Co(NH3)4Cl2]+. The corresponding ethylenediamine complexes are also well known. Analogues are known where the halides are replaced by nitrite, hydroxide, carbonate, etc. Alfred Werner worked extensively on these complexes in his Nobel-prize winning work.[25] The robustness of these complexes is demonstrated by the optical resolution of tris(ethylenediamine)cobalt(III) ([Co(en)
3]3+
).[26]
Cobalt(II) forms a wide variety of complexes, but mainly with weakly basic ligands. The pink-colored cation hexaaquocobalt(II) [Co(H2O)6]2+ is found in several routine cobalt salts such as the nitrate and sulfate. Upon addition of excess chloride, solutions of the hexaaquo complex converts to the deep blue CoCl2−4, which is tetrahedral.[citation needed]
Softer ligands like triphenylphosphine form complexes with Co(II) and Co(I), examples being bis- and tris(triphenylphosphine)cobalt(I) chloride, CoCl2(PPh3)2 and CoCl(PPh3)3. These Co(I) and Co(II) complexes represent a link to the organometallic complexes described below.[citation needed]
Organometallic compounds
[edit]
Cobaltocene is a structural analog to ferrocene, with cobalt in place of iron. Cobaltocene is much more sensitive to oxidation than ferrocene.[27] Cobalt carbonyl (Co2(CO)8) is a catalyst in carbonylation and hydrosilylation reactions.[28] Vitamin B12 (see below) is an organometallic compound found in nature and is the only vitamin that contains a metal atom.[29] 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,[30] 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.[31]
Isotopes
[edit]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 271.81 days; 56Co has a half-life of 77.24 days; and 58Co has a half-life of 70.84 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.[32]
The isotopes of cobalt range from 50Co to 73Co. The primary decay mode for isotopes with atomic masses 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 that is beta decay. The primary decay products below 59Co are element 26 (iron) isotopes; above that the decay products are element 28 (nickel) isotopes.[32]
Because 59Co has a nuclear spin, it is possible to detect it using nuclear magnetic resonance.[33] The nucleus has a magnetic quadrupole moment. Among all NMR active nuclei, 59Co has the largest chemical shift range and the chemical shift can be correlated with the spectrochemical series.[34] Resonances are observed over a range of 20000 ppm, the width of the signals being up to 20 kHz. A widely used standard is potassium hexacyanocobaltate (0.1M K3Co(CN)6 in D2O), which, due to its high symmetry, has a rather small line width. Systems of low symmetry can yield broadened signals to an extent that renders the signals unobservable in fluid phase NMR, but still observable in solid state NMR.
Etymology
[edit]Many different stories about the origin of the word "cobalt" have been proposed. In one version the element cobalt was named after "kobelt", the name which 16th century German silver miners had given to a nuisance type of ore which occurred that was corrosive and issued poisonous gas.[35][36] Although such ores had been used for blue pigmentation since antiquity, the Germans at that time did not have the technology to smelt the ore into metal (cf. § History below).[37]
The authority on such kobelt ore (Latinized as cobaltum or cadmia[38][39]) at the time was Georgius Agricola.[35][37] He was also the oft-quoted authority on the mine spirits called "kobel" (Latinized as cobalus or pl. cobali) in a separate work.[40][41][42]
Agricola did not make a connection between the similarly named ore and spirit. However, a causal connection (ore blamed on "kobel") was made by a contemporary,[44] and a word origin connection (word "formed" from cobalus) made by a late 18th century writer.[45] Later, Grimms' dictionary (1868) noted the kobalt/kobelt ore was blamed on the mountain spirit (Bergmännchen[b]) which was also held responsible for "stealing the silver and putting out an ore that caused poor mining atmosphere (Wetter[46]) and other health hazards".[36]
Grimms' dictionary entries equated the word "kobel" with "kobold", and listed it as a mere variant diminutive,[48] but the latter is defined in it as a household spirit.[47] Whereas some of the more recent commentators prefer to characterize the ore's namesake kobelt (recté kobel) as a gnome.[49][52]
The early 20th century Oxford English Dictionary (1st edition, 1908) had upheld Grimm's etymology.[c][53] However, by around the same time in Germany, the alternate etymology not endorsed by Grimm (kob/kof "house, chamber" + walt "power, ruler") was being proposed as more convincing.[54][55]
Somewhat later, Paul Kretschmer (1928) explained that while this "house ruler" etymology was the proper one that backed the original meaning of kobold as household spirit, a corruption later occurred introducing the idea of "mine demon" to it.[56] The present edition of the Etymologisches Wörterbuch (25th ed., 2012) under "kobold" lists the latter, not Grimm's etymology, but still persists, under its entry for "kobalt", that while the cobalt ore may have got its name from "a type of mine spirit/demon" (daemon metallicus) while stating that this is "apparently" the kobold.[57]
Joseph William Mellor (1935) also stated that cobalt may derive from kobalos (κόβαλος), though other theories had been suggested.[58]
Alternate theories
[edit]Several alternative etymologies that have been suggested, which may not involve a spirit (kobel or kobold) at all. Karl Müller-Fraureuth conjectured that kobelt derived from Kübel, a bucket used in mining, frequently mentioned by Agricola,[54] namely the kobel/köbel (Latinized as modulus).[59]
Another theory given by the Etymologisches Wörterbuch derives the term from kōbathium[57] or rather cobathia (κωβάθια, "arsenic sulfide"[60]) which occurs as noxious fumes.[37]
An etymology from Slavonic kowalti was suggested by Emanuel Merck (1902).[61][58]
W. W. Skeat and J. Berendes construed κόβαλος as "parasite", i.e. as an ore parasitic to nickel,[58] but this explanation is faulted for its anachronism since nickel was not discovered until 1751.[62][63]
History
[edit]
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).[64]
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.[65][66] 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 Egyptians sourced this cobalt from cobaltiferous alums found in Egypt's Western Oases.[67]
The word cobalt is derived from the 16th century German "kobelt", a type of ore, as aforementioned. 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.[68] Paracelsus, Georgius Agricola, and Basil Valentine all referred to such silicates as "cobalt".[69]
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",[70][71] naming it for the mineral from which he had extracted it.[72]: 153 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 previously known metals (iron, copper, silver, gold, zinc, mercury, tin, lead and bismuth) had no recorded discoverers.[73]
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.[74][75] 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, mining operations shifted again.[68] When the Shaba conflict started in 1978, the copper mines of Katanga Province nearly stopped production.[76][77] 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.[76][77]
In 1938, John Livingood and Glenn T. Seaborg discovered the radioisotope cobalt-60.[78] This isotope was famously used at Columbia University in the 1950s to establish parity violation in radioactive beta decay.[79][80]
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 US. High purity cobalt was highly sought after for its use in jet engines and gas turbines.[81] An adequate supply of the ore was found in Idaho near Blackbird canyon. Calera Mining Company started production at the site.[82]
Cobalt demand has further accelerated in the 21st century as an essential constituent of materials used in rechargeable batteries, superalloys, and catalysts.[81] 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.[83]
Occurrence
[edit]The stable form of cobalt is produced in supernovae through the r-process.[84] It comprises 0.0029% of the Earth's crust. Except as recently delivered in meteoric iron, free cobalt (the native metal) is not found on Earth's surface because of its tendency to react with oxygen in the atmosphere. Small amounts of cobalt compounds are found in most rocks, soils, plants, and animals.[85] In the ocean cobalt typically reacts with chlorine.
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.[86]
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.[19] The mineral cattierite is similar to pyrite and occurs together with vaesite in the copper deposits of Katanga Province.[87] When it reaches the atmosphere, weathering occurs; the sulfide minerals oxidize and form pink erythrite ("cobalt glance": Co3(AsO4)2·8H2O) and spherocobaltite (CoCO3).[88][89]
Cobalt is also a constituent of tobacco smoke.[90] 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.[91]
Production
[edit]
| Country | Production | Reserves |
|---|---|---|
| 130,000 | 4,000,000 | |
| 10,000 | 600,000 | |
| 8,900 | 250,000 | |
| 5,900 | 1,500,000 | |
| 3,900 | 220,000 | |
| 3,800 | 500,000 | |
| 3,800 | 260,000 | |
| 3,000 | 100,000 | |
| 3,000 | 47,000 | |
| 2,700 | 36,000 | |
| 2,300 | 13,000 | |
| 2,200 | 140,000 | |
| 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.[93][94]
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.[95]
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.[96][97]
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.[98]
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.[19]

Extraction
[edit]
The United States Geological Survey estimates world reserves of cobalt at 11,000,000 metric tons.[99] 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.[100]
Democratic Republic of the Congo
[edit]
Changes that Congo made to mining laws in 2002[further explanation needed] attracted new investments in Congolese copper and cobalt projects.[101] 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.[102]
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.[103] 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.[104]
In 2016, Chinese ownership of cobalt production in the Congo was estimated at over 10% of global cobalt supply, forming a key input to the Chinese cobalt refining industry and granting China substantial influence over the global cobalt supply chain.[105] Chinese control of Congolese cobalt has raised concern in Western nations which have sought to reduce supply chain reliance upon China and have expressed concern regarding labor and human rights violations in cobalt mines in the DRC.[106][107]
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.[101][108] 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.[95]
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.[109]
On 9 March 2018, President Joseph Kabila updated the 2002 mining code, increasing royalty charges and declaring cobalt and coltan "strategic metals".[110][111] The 2002 mining code was effectively updated on 4 December 2018.[112]
In February 2025, the DRC implemented a four-month suspension of cobalt exports, citing an oversupply of the metal amid a price decline to its lowest level in 21 years. Cobalt, a key byproduct of copper mining, is an essential material in battery technology. The DRC accounts for approximately 75 percent of the global supply. Within the country, the China Molybdenum Company (CMOC) dominates the industry, contributing roughly 40 percent of the world's cobalt production. Over the past year, CMOC has significantly increased its output, doubling production from two of its mines in the DRC from 56,000 tonnes to 114,000 tonnes.[citation needed]
Labor conditions
[edit]Artisanal mining supplied 17% to 40% of the DRC production as of 2016.[113] 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.[114] 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.[115]
Child labor is used in mining cobalt from African artisanal mines.[113][116] Human rights activists have highlighted this and investigative journalism reporting has confirmed it.[117][118] This revelation prompted cell phone maker Apple Inc., on 3 March 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.[119][120] In 2023, Apple announced it would convert to using recycled cobalt by 2025.[121]
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 and Glencore are participating in several initiatives, such as the Responsible Cobalt Initiative[122] and Cobalt for Development[123] 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.[124]
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.[125]
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.[126] The companies in question denied their involvement in child labour.[127] In 2024 the court ruled that the suppliers facilitate force labor but the US tech companies are not liable because they don't operate as a shared enterprise with the suppliers and that the "alleged injuries are not fairly traceable" to any of the defendants' conduct.[128] The book Cobalt Red[129][130] alleges that workers including children suffer injuries, amputations, and death as the result of the hazardous working conditions and mine tunnel collapses during artisanal mining of cobalt in the DRC.[131]
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[132] 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.[133] After oversupply, the price dropped to a more normal $15 in 2019.[134][135] 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.[136][137]
Canada
[edit]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.[138]
Cobalt mined in Canada is a by-product of nickel mining. Even so, in 2023 the country produced more than 5,000 tons of cobalt (43% is mined in Newfoundland and Labrador, the rest in Ontario, Manitoba and Quebec). Exports of cobalt and cobalt products totaled $568 million in 2023.[139]
Cuba
[edit]Canada's Sherritt International processes cobalt ores in nickel deposits from the Moa mines in Cuba, and the island has several others mines in Mayarí, Camagüey, and Pinar del Río. 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.[140]
Indonesia
[edit]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.[141] Cobalt production increased from 1,300 tons to 20,500 tons between 2015 and 2024 due to the Indonesian government's strategic initiative to develop a robust domestic supply chain for electric vehicles. An export ban in 2020 has ensured an influx of foreign investment in nickel and cobalt processing in the country.[11]
Applications
[edit]In 2016, 116,000 tonnes (128,000 short tons) of cobalt was used.[10] Cobalt has been used in the production of high-performance alloys.[93][94] It is also used in some rechargeable batteries.
Alloys
[edit]Cobalt-based superalloys have historically consumed most of the cobalt produced.[93][94] 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.[142] Cobalt-based alloys are also corrosion- and wear-resistant, making them, like titanium, useful for making orthopedic implants that do not 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.[143] Special cobalt-chromium-molybdenum alloys like Vitallium are used for prosthetic parts (hip and knee replacements).[144] Cobalt alloys are also used for dental prosthetics as a useful substitute for nickel, which may be allergenic.[145] 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.[146] It is also alloyed with 95% platinum for jewelry, yielding an alloy suitable for fine casting, which is also slightly magnetic.[147] In addition to structural and magnetic roles, cobalt alloys are critical in aerospace-grade electrical components. They are used in connectors, thermal switches, and microsensors that must endure extreme temperatures, vibration, and radiation—conditions typical in satellites, fighter aircraft, and hypersonic systems.[148] These alloys maintain conductivity and mechanical integrity even under fluctuating mission-critical loads.[149]
Batteries
[edit]Lithium cobalt oxide (LiCoO2, aka "LCO"), first sold commercially in 1991 by Sony, was widely used in lithium-ion battery cathodes until the 2010s. The material is composed of cobalt oxide layers with the lithium intercalated. These LCO batteries continue to dominate the market for consumer electronics. Batteries for electric cars however have shifted to lower cobalt technologies.[150]
In 2018 most cobalt in batteries was used in a mobile device,[151] a more recent application for cobalt is rechargeable batteries for electric cars. This industry increased five-fold in its demand for cobalt from 2016 to 2020, which made it urgent to find new raw materials in more stable areas of the world.[152] Demand is expected to continue or increase as the prevalence of electric vehicles increases.[153] Exploration in 2016–2017 included the area around Cobalt, Ontario, an area where many silver mines ceased operation decades ago.[152] 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.[154][155]
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.[156][157] Research was also conducted by the European Union into the possibility of eliminating cobalt requirements in lithium-ion battery production.[158][159] In September 2020, Tesla outlined their plans to make their own, cobalt-free battery cells.[160]
Nickel–cadmium[161] (NiCd) and nickel metal hydride[162] (NiMH) batteries also included cobalt to improve the oxidation of nickel in the battery.[161] 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.[163]
Catalysts
[edit]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.[164][165] However, their use is being phased out due to toxicity concerns.[166] 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.[167][168][169]
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.[170] Hydroformylation of alkenes often uses cobalt octacarbonyl as a catalyst.[171] 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.[165]
Pigments and coloring
[edit]

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.[172] Smalt was widely used to color glass and as pigment for paintings.[173] In 1780, Sven Rinman discovered cobalt green, and in 1802 Louis Jacques Thénard discovered cobalt blue.[174] 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.[175][176]
Radioisotopes
[edit]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.[32][177]
Cobalt is used in external beam radiotherapy, sterilization of medical supplies and medical waste, radiation treatment of foods for sterilization (cold pasteurization),[178] 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.[179][180]
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.[181] Cobalt-57 (Co-57 or 57Co) is a cobalt radioisotope most often used in medical tests, as a radiolabel for vitamin B 12 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.[182][183]
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.[184][185]
Magnetic materials
[edit]Due to the ferromagnetic properties of cobalt, it is used in the production of various magnetic materials.[186] It is used in creating permanent magnets like Alnico magnets, known for their strong magnetic properties used in electric motors, sensors, and MRI machines.[187][188] It is also used in production of magnetic alloys like cobalt steel, widely used in magnetic recording media such as hard disks and tapes.[189]
Cobalt's ability to maintain magnetic properties at high temperatures makes it valuable in magnetic recording applications, ensuring reliable data storage devices.[190] Cobalt also contributes to specialized magnets such as samarium-cobalt magnets, which are vital in electronics for components like sensors and actuators.[191]
Other uses
[edit]- Cobalt is used in electroplating for its attractive appearance, hardness, and resistance to oxidation.[192]
- It is also used as a base primer coat for porcelain enamels.[193]
Biological role
[edit]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.[194][195] 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.[196]
Proteins based on cobalamin use corrin to hold the cobalt. Coenzyme B12 features a reactive C-Co bond that participates in the reactions.[197] 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.[198]
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.[199]
Cobalt deficiency
[edit]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.[200][201] 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.[clarification needed][202][201][203]
-
Cobalt-deficient sheep
Health issues
[edit]| Hazards | |
|---|---|
| GHS labelling:[204] | |
| Danger | |
| H302, H317, H319, H334, H341, H350, H360F, H412 | |
| P273, P280, P301+P312, P302+P352, P305+P351+P338, P308+P313 | |
| NFPA 704 (fire diamond) | |
The LD50 value for soluble cobalt salts has been estimated to be between 150 and 500 mg/kg.[205] 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.[206]
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.[207][208]
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.[209]
It causes respiratory problems when inhaled.[210] It also causes skin problems when touched; after nickel and chromium, cobalt is a major cause of contact dermatitis.[211]
Notes
[edit]- ^ The thermal expansion of cobalt is anisotropic: the coefficients for each crystal axis are (at 20 °C): αa = 10.9×10−6/K, αc = 17.9×10−6/K, and αaverage = αV/3 = 12.9×10−6/K.
- ^ Grimm's dictionary more specifically calls it "spectral mountain manikin" (gespenstisches Bergmännchen), elsewhere ("Kobold" II) it is notes kobold also refers to Berggeist in bergmännisch (miners' lingo).
- ^ Grimm derived and kobold from Greek kobalos, as aforestated; the OED concurred that kobold, kobelt (ore), kobel (mine spirit) were the same word.
References
[edit]- ^ "cobalt". Oxford English Dictionary (2nd ed.). Oxford University Press. 1989.
- ^ "Standard Atomic Weights: Cobalt". CIAAW. 2017.
- ^ Prohaska, Thomas; Irrgeher, Johanna; Benefield, Jacqueline; Böhlke, John K.; Chesson, Lesley A.; Coplen, Tyler B.; Ding, Tiping; Dunn, Philip J. H.; Gröning, Manfred; Holden, Norman E.; Meijer, Harro A. J. (4 May 2022). "Standard atomic weights of the elements 2021 (IUPAC Technical Report)". Pure and Applied Chemistry. doi:10.1515/pac-2019-0603. ISSN 1365-3075.
- ^ a b Arblaster, John W. (2018). Selected Values of the Crystallographic Properties of Elements. Materials Park, Ohio: ASM International. ISBN 978-1-62708-155-9.
- ^ Co(–3) is known in Na3Co(CO)3; see John E. Ellis (2006). "Adventures with Substances Containing Metals in Negative Oxidation States". Inorganic Chemistry. 45 (8): 3167–3186. doi:10.1021/ic052110i.
- ^ a b c d Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. p. 28. doi:10.1016/C2009-0-30414-6. ISBN 978-0-08-037941-8.
- ^ a b c d Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 1117–1119. doi:10.1016/C2009-0-30414-6. ISBN 978-0-08-037941-8.
- ^ Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S.; Audi, G. (2021). "The NUBASE2020 evaluation of nuclear properties" (PDF). Chinese Physics C. 45 (3) 030001. doi:10.1088/1674-1137/abddae.
- ^ "cobalt". Oxford English Dictionary (2nd ed.). Oxford University Press. 1989.
- ^ a b Danielle Bochove (1 November 2017). "Electric car future spurs Cobalt rush: Swelling demand for product breathes new life into small Ontario town". Vancouver Sun. Bloomberg. Archived from the original on 28 July 2019.
- ^ a b GlobalData (17 January 2025). "Global cobalt supply to surpass 300kt mark in 2024, driven by production from the DRC and Indonesia". Mining Technology. Retrieved 20 April 2025.
- ^ "Catalysts". Cobalt Institute. Archived from the original on 16 August 2023. Retrieved 15 August 2023.
- ^ Enghag, Per (2004). "Cobalt". Encyclopedia of the elements: technical data, history, processing, applications. Wiley. p. 667. ISBN 978-3-527-30666-4.
- ^ Murthy, V. S. R (2003). "Magnetic Properties of Materials". Structure And Properties of Engineering Materials. McGraw-Hill Education (India) Pvt Limited. p. 381. ISBN 978-0-07-048287-6.
- ^ Celozzi, Salvatore; Araneo, Rodolfo; Lovat, Giampiero (1 May 2008). Electromagnetic Shielding. Wiley. p. 27. ISBN 978-0-470-05536-6.
- ^ Lee, B.; Alsenz, R.; Ignatiev, A.; Van Hove, M.; Van Hove, M. A. (1978). "Surface structures of the two allotropic phases of cobalt". Physical Review B. 17 (4): 1510–1520. Bibcode:1978PhRvB..17.1510L. doi:10.1103/PhysRevB.17.1510.
- ^ "Properties and Facts for Cobalt". American Elements. Archived from the original on 2 October 2008. Retrieved 19 September 2008.
- ^ Cobalt. Brussels: Centre d'Information du Cobalt. 1966. p. 45.
- ^ a b c d e Holleman, A. F.; Wiberg, E.; Wiberg, N. (2007). "Cobalt". Lehrbuch der Anorganischen Chemie (in German) (102nd ed.). de Gruyter. pp. 1146–1152. ISBN 978-3-11-017770-1.
- ^ Housecroft, C. E.; Sharpe, A. G. (2008). Inorganic Chemistry (3rd ed.). Prentice Hall. p. 722. ISBN 978-0-13-175553-6.
- ^ Rutley, Frank (6 December 2012). Rutley's Elements of Mineralogy. Springer Science & Business Media. p. 40. ISBN 978-94-011-9769-4.
- ^ Krebs, Robert E. (2006). The history and use of our earth's chemical elements: a reference guide (2nd ed.). Greenwood Publishing Group. p. 107. ISBN 0-313-33438-2.
- ^ Petitto, Sarah C.; Marsh, Erin M.; Carson, Gregory A.; Langell, Marjorie A. (2008). "Cobalt oxide surface chemistry: The interaction of CoO(100), Co3O4(110) and Co3O4(111) with oxygen and water". Journal of Molecular Catalysis A: Chemical. 281 (1–2): 49–58. doi:10.1016/j.molcata.2007.08.023. S2CID 28393408.
- ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. pp. 1119–1120. doi:10.1016/C2009-0-30414-6. ISBN 978-0-08-037941-8.
- ^ Werner, A. (1912). "Zur Kenntnis des asymmetrischen Kobaltatoms. V". Chemische Berichte. 45: 121–130. doi:10.1002/cber.19120450116.
- ^ Gispert, Joan Ribas (2008). "Early Theories of Coordination Chemistry". Coordination chemistry. Wiley. pp. 31–33. ISBN 978-3-527-31802-5. Archived from the original on 5 May 2016. Retrieved 27 June 2015.
- ^ House, James e. (2008). Inorganic chemistry. Academic Press. p. 767. ISBN 978-0-12-356786-4. Retrieved 16 May 2011.
- ^ Starks, Charles M.; Liotta, Charles Leonard; Halpern, Marc (1994). Phase-transfer catalysis: fundamentals, applications, and industrial perspectives. Springer. p. 600. ISBN 978-0-412-04071-9. Retrieved 16 May 2011.
- ^ Sigel, Astrid; Sigel, Helmut; Sigel, Roland, eds. (2010). Organometallics in Environment and Toxicology (Metal Ions in Life Sciences). Cambridge, UK: Royal Society of Chemistry Publishing. p. 75. ISBN 978-1-84755-177-1.
- ^ Byrne, Erin K.; Richeson, Darrin S.; Theopold, Klaus H. (1 January 1986). "Tetrakis(1-norbornyl)cobalt, a low spin tetrahedral complex of a first row transition metal". Journal of the Chemical Society, Chemical Communications (19): 1491. doi:10.1039/C39860001491. ISSN 0022-4936.
- ^ Byrne, Erin K.; Theopold, Klaus H. (1 February 1987). "Redox chemistry of tetrakis(1-norbornyl)cobalt. Synthesis and characterization of a cobalt(V) alkyl and self-exchange rate of a Co(III)/Co(IV) couple". Journal of the American Chemical Society. 109 (4): 1282–1283. doi:10.1021/ja00238a066. ISSN 0002-7863.
- ^ a b c Kondev, F. G.; Wang, M.; Huang, W. J.; Naimi, S.; Audi, G. (2021). "The NUBASE2020 evaluation of nuclear properties" (PDF). Chinese Physics C. 45 (3) 030001. doi:10.1088/1674-1137/abddae.
- ^ Chan J, Auyeung S (2000). "Cobalt-59 NMR spectroscopy". In Webb GA (ed.). Annual Reports on NMR Spectroscopy. Vol. 41. Elsevier. pp. 1–54. doi:10.1016/S0066-4103(00)41008-2. ISBN 978-0-12-505341-9.
- ^ Yamasaki, A (1991). "Cobalt-59 Nuclear Magnetic Resonance Spectroscopy in Coordination Chemistry". Journal of Coordination Chemistry. 24 (3): 211–260. doi:10.1080/00958979109407886.
- ^ a b c Ball, Philip (2003). Bright Earth: Art and the Invention of Color. University of Chicago Press. pp. 118–119. ISBN 9780226036281.
- ^ a b c Grimms; Hildebrand, Rudolf (1868). Deutsches Wörterbuch, Band 5, s.v. "Kobalt"
- ^ a b c d e f Wothers, Peter (2019). Antimony, Gold, and Jupiter's Wolf: How the elements were named. Oxford University Press. pp. 47–49. ISBN 9780192569905.
- ^ Agricola, Georgius (1546) [1530]. "Bermannus, sive de re metallica dialogus". Georgii Agricolae De ortu & causis subterraneorum lib. 5. De natura eorum quae effluunt ex terra lib. 4. De natura fossilium lib. 10. De ueteribus & nouis metallis lib. 2. Bermannus, siue De re metallica dialogus lib.1. Interpretatio Germanica uocum rei metallicæ, addito Indice fœcundissimo. Basel: Froben. pp. 441–442.
cobaltum nostri uocant, Græci cadmiam
; Cf. index under "cobaltum". - ^ Agricola, Georgius (1912). Georgius Agricola De Re Metallica: Tr. from the 1st Latin Ed. of 1556 (Books I–VIII). Translated by Hoover, Herbert Clark and Lou Henry Hoover. London: The Mining Magazine. pp. 112–113. Describes (and tabulates) German form kobelt; In two volumes: Second Part, Books IX–XII, contiguous pagination.
- ^ Agricola, Georgius (1614) [1549]. "37". In Johannes Sigfridus (ed.). Georgii Agricolae De Animantibus subterraneis. Witebergæ: Typis Meisnerianis. pp. 78–79.
- ^ a b Agricola, Georgius (1657) [1530]. "Animantium nomina latina, graega, q'ue germanice reddita, quorum author in Libro de subterraneis animantibus meminit". Georgii Agricolae Kempnicensis Medici Ac Philosophi Clariss. De Re Metallica Libri XII.: Quibus Officia, Instrumenta, Machinae, Ac Omnia Denique Ad Metallicam Spectantia, Non Modo Luculentissime describuntur; sed & per effigies, suis locis insertas ... ita ob oculos ponuntur, ut clarius tradi non possint. Basel: Sumptibus & Typis Emanuelis König. p. [762].
Dæmonum: Dæmon subterraneus trunculentus: bergterufel; mitis bergmenlein/kobel/guttel
- ^ This passage from the separate work, de animantibus is translated in footnote by the Agricola & Hoovers trr. (1912), p. 217, n26: "the Germans as well as the Greeks call cobalos".
- ^ Agricola & Hoovers trr. (1912), p. 214, n21.
- ^ Lutheran reformist theologian Johannes Mathesius's sermon (1652) on the nuisance kobelt ore believed caused by a demon known to the masses as kobel. Quoted in English by the Hoovers,[43] excerpted by Wothers.[37]
- ^ Johann Beckmann (Eng. tr. 1797), who did explicitly comment on the derivation of the word for "cobalt" ore as formed from kobel (Agricola's cobalus) has been cited by chemist Peter Wothers on this topic.[37]
- ^ "New and complete dictionary of the German language for Englishmen" s.v. "Das Wetter": "4. Air and vapours, damps, steams... among Miners", Küttner, Carl Gottlob; Nicholson, William, edd. (1813), vol. 3.
- ^ a b Grimms; Hildebrand, Rudolf (1868). Deutsches Wörterbuch, Band 5, s.v. "Kobold" at "III. 3) nebenformen"
- ^ Grimms dictionary states that kobalt and kobold are "the same word at its original source (ursprünglich)".[36] Also, Grimm's entry in "kobold", III. ursprung, nebenformen, 3) a) lists kobel as a diminutive Nebenname.[47]
- ^ Actually, among "gnomes and goblins".[35][37]
- ^ Lecouteux, Claude (2016). "BERGMÄNNCHEN (Bergmännlein, Bergmönch, Knappenmanndl, Kobel, Gütel; gruvrå in Sweden)". Encyclopedia of Norse and Germanic Folklore, Mythology, and Magic. Simon and Schuster. ISBN 9781620554814., cf. (in French) Lecouteux (2014), "BERGMÄNNCHEN", Dictionnaire de mythologie germanique, pp. 1995–1996.
- ^ Verardi, Donato (2023). Aristotelianism and Magic in Early Modern Europe: Philosophers, Experimenters and Wonderworkers. Bloomsbury Publishing. p. 85. ISBN 9781350357174.
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- ^ Kobayashi, Michihiko; Shimizu, Sakayu (1999). "Cobalt proteins". European Journal of Biochemistry. 261 (1): 1–9. doi:10.1046/j.1432-1327.1999.00186.x. PMID 10103026.
- ^ "Soils". Waikato University. Archived from the original on 25 January 2012. Retrieved 16 January 2012.
- ^ a b McDowell, Lee Russell (2008). Vitamins in Animal and Human Nutrition (2nd ed.). Hoboken: John Wiley & Sons. p. 525. ISBN 978-0-470-37668-3.
- ^ Australian Academy of Science > Deceased Fellows > Hedley Ralph Marston 1900–1965 Accessed 12 May 2013.
- ^ Snook, Laurence C. (1962). "Cobalt: its use to control wasting disease". Journal of the Department of Agriculture, Western Australia. 4. 3 (11): 844–852.
- ^ "Cobalt 356891". Sigma-Aldrich. 14 October 2021. Retrieved 22 December 2021.
- ^ Donaldson, John D. and Beyersmann, Detmar (2005) "Cobalt and Cobalt Compounds" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim. doi:10.1002/14356007.a07_281.pub2
- ^ NIOSH Pocket Guide to Chemical Hazards. "#0146". National Institute for Occupational Safety and Health (NIOSH).
- ^ Morin Y; Tětu A; Mercier G (1969). "Quebec beer-drinkers' cardiomyopathy: Clinical and hemodynamic aspects". Annals of the New York Academy of Sciences. 156 (1): 566–576. Bibcode:1969NYASA.156..566M. doi:10.1111/j.1749-6632.1969.tb16751.x. PMID 5291148. S2CID 7422045.
- ^ Barceloux, Donald G. & Barceloux, Donald (1999). "Cobalt". Clinical Toxicology. 37 (2): 201–216. doi:10.1081/CLT-100102420. PMID 10382556.
- ^ [PDF]
- ^ Elbagir, Nima; van Heerden, Dominique; Mackintosh, Eliza (May 2018). "Dirty Energy". CNN. Retrieved 30 May 2018.
- ^ Basketter, David A.; Angelini, Gianni; Ingber, Arieh; Kern, Petra S.; Menné, Torkil (2003). "Nickel, chromium and cobalt in consumer products: revisiting safe levels in the new millennium". Contact Dermatitis. 49 (1): 1–7. doi:10.1111/j.0105-1873.2003.00149.x. PMID 14641113. S2CID 24562378.
Further reading
[edit]
- Harper, E. M.; Kavlak, G.; Graedel, T. E. (2012). "Tracking the metal of the goblins: Cobalt's cycle of use". Environmental Science & Technology. 46 (2): 1079–86. Bibcode:2012EnST...46.1079H. doi:10.1021/es201874e. PMID 22142288. S2CID 206948482.
- Narendrula, R.; Nkongolo, K. K.; Beckett, P. (2012). "Comparative soil metal analyses in Sudbury (Ontario, Canada) and Lubumbashi (Katanga, DR-Congo)". Bulletin of Environmental Contamination and Toxicology. 88 (2): 187–92. Bibcode:2012BuECT..88..187N. doi:10.1007/s00128-011-0485-7. PMID 22139330. S2CID 34070357.
- Pauwels, H.; Pettenati, M.; Greffié, C. (2010). "The combined effect of abandoned mines and agriculture on groundwater chemistry". Journal of Contaminant Hydrology. 115 (1–4): 64–78. Bibcode:2010JCHyd.115...64P. doi:10.1016/j.jconhyd.2010.04.003. PMID 20466452.
- Bulut, G. (2006). "Recovery of copper and cobalt from ancient slag". Waste Management & Research. 24 (2): 118–24. Bibcode:2006WMR....24..118B. doi:10.1177/0734242X06063350. PMID 16634226. S2CID 24931095.
- Jefferson, J. A.; Escudero, E.; Hurtado, M. E.; Pando, J.; Tapia, R.; Swenson, E. R.; Prchal, J.; Schreiner, G. F.; Schoene, R. B.; Hurtado, A.; Johnson, R. J. (2002). "Excessive erythrocytosis, chronic mountain sickness, and serum cobalt levels". Lancet. 359 (9304): 407–8. doi:10.1016/s0140-6736(02)07594-3. PMID 11844517. S2CID 12319751.
- Løvold, T. V.; Haugsbø, L. (1999). "Cobalt mining factory--diagnoses 1822-32". Tidsskrift for den Norske Laegeforening. 119 (30): 4544–6. PMID 10827501.
- Bird, G. A.; Hesslein, R. H.; Mills, K. H.; Schwartz, W. J.; Turner, M. A. (1998). "Bioaccumulation of radionuclides in fertilized Canadian Shield lake basins". The Science of the Total Environment. 218 (1): 67–83. Bibcode:1998ScTEn.218...67B. doi:10.1016/s0048-9697(98)00179-x. PMID 9718743.
- Nemery, B. (1990). "Metal toxicity and the respiratory tract". The European Respiratory Journal. 3 (2): 202–19. doi:10.1183/09031936.93.03020202. PMID 2178966.
- Kazantzis, G. (1981). "Role of cobalt, iron, lead, manganese, mercury, platinum, selenium, and titanium in carcinogenesis". Environmental Health Perspectives. 40: 143–61. Bibcode:1981EnvHP..40..143K. doi:10.1289/ehp.8140143. PMC 1568837. PMID 7023929.
- Kerfoot, E. J.; Fredrick, W. G.; Domeier, E. (1975). "Cobalt metal inhalation studies on miniature swine". American Industrial Hygiene Association Journal. 36 (1): 17–25. doi:10.1080/0002889758507202. PMID 1111264.
External links
[edit]- . Encyclopædia Britannica. Vol. VI (9th ed.). 1878. pp. 81–83.
- Cobalt at The Periodic Table of Videos (University of Nottingham)
- Centers for Disease and Prevention – Cobalt
- usgs.gov (Mineral Commodity Summaries 2025): Cobalt
Cobalt
View on GrokipediaProperties
Physical and atomic properties
Cobalt is a chemical element with symbol Co and atomic number 27.[7] Its standard atomic weight is 58.933194(4).[8] The ground-state electron configuration of the cobalt atom is [Ar] 3d7 4s2.[7] Cobalt is a transition metal that occurs as a hard, lustrous, bluish-gray solid under standard conditions.[9] It has a density of 8.90 g/cm3 at 20 °C.[8] The melting point is 1495 °C and the boiling point is 2927 °C.[8] Cobalt exhibits a Mohs hardness of 5, Vickers hardness of 1043 MPa, and Brinell hardness of 700 MPa.[8] At room temperature, elemental cobalt adopts a hexagonal close-packed crystal structure (alpha phase), with space group P63/mmc and lattice parameters a = 250.71 pm, c = 406.73 pm.[10] Above 422 °C, it transitions to a face-centered cubic structure (beta phase).[11] Cobalt is ferromagnetic, with a Curie temperature of 1115–1131 °C above which it loses its permanent magnetism.[12] This property arises from the alignment of unpaired d-electrons in its atomic structure, contributing to its use in magnetic alloys.[13]Isotopes
Cobalt occurs naturally as a single stable isotope, cobalt-59 (⁵⁹Co), which accounts for 100% of its elemental abundance in the Earth's crust. This isotope has an atomic mass of 58.933198 u, a nuclear spin of 7/2, and a magnetic moment of +4.627 nuclear magnetons.[14][15] Cobalt-59 is monoisotopic for the element, meaning no other stable isotopes exist, and its atomic weight determines the standard atomic mass of cobalt at 58.933194(3) u.[16] All other cobalt isotopes are radioactive and synthetic, with 22 characterized radioisotopes having mass numbers from 48Co to 69Co. These decay primarily via beta minus emission, electron capture, or beta plus emission, with half-lives ranging from microseconds to years; most shorter-lived isotopes have half-lives under 80 days.[17][18] The longest-lived radioactive isotope, cobalt-60 (⁶⁰Co), has a half-life of 5.2714 years and is generated by neutron activation of ⁵⁹Co in nuclear reactors, where it captures a neutron to form ⁶⁰Co. It decays by beta emission to stable nickel-60, emitting high-energy gamma rays (1.17 and 1.33 MeV), making it valuable for gamma radiography to detect material flaws, food and medical sterilization, and external beam radiotherapy for cancer treatment.[19][18][20] Other significant radioisotopes include cobalt-57 (⁵⁷Co), with a half-life of 271.79 days, which undergoes electron capture decay and emits gamma rays suitable for medical imaging, such as in single-photon emission computed tomography (SPECT) for organ function studies and as a calibration standard for dose calibrators.[21] Cobalt-56 (⁵⁶Co) has a half-life of 77.2 days and is observed in supernova remnants as a decay product influencing light curves. Shorter-lived isotopes like ⁵⁸Co (half-life 70.9 days) arise as fission products or activation byproducts in reactors but have limited practical applications due to rapid decay.[18]| Isotope | Half-life | Primary Decay Mode | Key Applications |
|---|---|---|---|
| ⁵⁹Co | Stable | N/A | Natural occurrence; NMR reference standard[15] |
| ⁶⁰Co | 5.2714 years | β⁻, γ | Radiotherapy, industrial sterilization, radiography[19][20] |
| ⁵⁷Co | 271.79 days | EC, γ | Medical imaging, calibration sources[21] |
| ⁵⁶Co | 77.2 days | β⁻, γ, EC | Astrophysical studies (supernovae)[18] |
Chemical reactivity and compounds
Cobalt exhibits moderate chemical reactivity as a transition metal. It does not react with water at room temperature but dissolves slowly in dilute acids such as sulfuric acid, producing hydrogen gas and aqueous Co(II) ions.[22] Upon heating in air, cobalt forms the mixed oxide Co₃O₄, which converts to CoO above 900°C.[22] In powder form, it burns brilliantly when exposed to air.[23] The element predominantly adopts +2 and +3 oxidation states in its compounds, with Co(II) being more stable in aqueous solutions and Co(III) requiring stabilization by ligands due to its oxidizing nature.[24] Higher states like +4 occur in certain fluorides, while lower states appear in organometallic complexes.[25] Common inorganic compounds include cobalt(II) oxide (CoO), a greenish-black solid used in ceramics, and cobalt(III) oxide (Co₂O₃), which decomposes to Co₃O₄ upon heating.[26] Cobalt(II) chloride (CoCl₂) forms a pink hexahydrate in water, turning anhydrous blue upon dehydration, and reacts with concentrated ammonia to yield hexaamminecobalt(II) chloride.[27] Cobalt(II) sulfate (CoSO₄) is employed in electroplating and as a mordant in dyeing.[26] Coordination compounds are prevalent, such as [Co(NH₃)₆]³⁺ for Co(III), which demonstrates ligand field effects influencing color and stability.[26] Cobalt aluminate (CoAl₂O₄), known as cobalt blue pigment, provides a stable deep blue color in glass and ceramics due to its spinel structure.[26] Organometallic derivatives, like cobaltocene (Co(C₅H₅)₂), exhibit reactivity akin to iron analogs but with distinct electronic properties from the d⁷ configuration.[25]History
Etymology and early recognition
The name cobalt originates from the German word Kobold, denoting a goblin or mischievous underground spirit, a term used by 16th-century silver miners in regions like Saxony to describe troublesome ores that emitted toxic arsenic vapors during smelting, resisted yielding precious metals, and instead afflicted workers with illness.[28][29][30] Cobalt compounds were employed in antiquity for producing vivid blue pigments in glass and ceramics, with evidence of their use appearing in Egyptian statuettes and beads from the 3rd millennium BCE, Roman-era glass from Pompeii, and early Chinese porcelain glazes dating to around 1335 CE.[25][31] Swedish chemist Georg Brandt first isolated metallic cobalt around 1735, demonstrating through experiments that it formed a distinct blue-tinted oxide responsible for coloring glass and minerals, separate from bismuth, copper, or iron.[1][7][32] Brandt's isolation involved reducing cobalt ore with charcoal, yielding a metal that resisted dissolution in acids unlike previously known substances, though initial scientific acceptance was delayed until Torbern Bergman's confirmation in 1780 established cobalt unequivocally as a novel element.[33][34]Industrial development and key milestones
Industrial applications of cobalt emerged in the early 20th century, transitioning from its longstanding use in pigments and ores to high-performance alloys that leveraged its hardness, magnetic properties, and heat resistance.[33] The first U.S. patent for a cobalt alloy was granted in 1907, enhancing machining tool productivity through improved wear resistance.[33] This marked the onset of cobalt's role in metallurgy, driven by demand for durable materials in manufacturing and emerging technologies. Key advancements accelerated during the interwar and World War II periods. In the 1930s, aluminum-nickel-cobalt (Alnico) permanent magnets were developed, offering superior magnetic strength for electrical and military applications.[35] Cobalt-chromium alloys, such as Stellite invented by Elwood Haynes around 1907 and refined thereafter, found use in cutting tools and later in medical implants like Vitallium by the 1930s.[36] Post-1940, cobalt-based superalloys proliferated for gas turbine engines, with British Rolls-Royce developing X-40 alloy containing 25% cobalt in 1940 to withstand temperatures up to 850°C in jet propulsion systems.[37] These innovations, spurred by aviation and defense needs, elevated cobalt from a byproduct of nickel and copper mining to a critical strategic metal.[38] The late 20th century introduced cobalt's pivotal role in electrochemistry. In 1980, researchers including John Goodenough developed lithium cobalt oxide (LiCoO2) cathodes, enabling higher energy density in rechargeable batteries.[39] Sony commercialized the first lithium-ion batteries using this material in 1991, powering portable electronics and foreshadowing explosive demand from electric vehicles.[40] Global cobalt consumption shifted dramatically, with battery applications comprising over 50% of demand by the 2010s, reflecting cobalt's enabling function in energy storage amid the transition to electrification.[33]Occurrence and Reserves
Natural distribution in Earth's crust
Cobalt occurs at low concentrations throughout the Earth's crust, with an estimated average abundance of 25 to 30 parts per million (ppm) by weight, ranking it approximately 33rd among elements in crustal composition.[41] [42] This value derives from geochemical models balancing upper and lower crustal compositions, though estimates for the upper continental crust alone are lower, around 17 to 20 ppm.[43] Concentrations vary widely due to cobalt's siderophile and lithophile affinities, leading to its preferential incorporation into ferromagnesian minerals during igneous processes. In igneous rocks, cobalt is markedly enriched in mafic and ultramafic varieties compared to felsic ones, reflecting its compatible behavior as a trace element that partitions into early-crystallizing phases. Ultramafic rocks such as peridotite and serpentinite average about 110 ppm, mafic rocks like basalt contain around 47 ppm, and felsic granites typically hold only 2 to 3 ppm.[41] [44] Cobalt substitutes for iron and magnesium in minerals including olivine, pyroxene, amphibole, and spinel, which dominate mafic-ultramafic lithologies.[41] During fractional crystallization, it depletes in residual felsic melts, explaining the low levels in granitic rocks. Sedimentary rocks show intermediate concentrations, with shales averaging 19 ppm due to adsorption onto clays and association with iron oxides, while sandstones and limestones contain less, often below 10 ppm.[44] In metamorphic rocks, cobalt follows protolith compositions, remaining elevated in amphibolites (around 48 ppm) derived from mafic sources.[41] Overall, cobalt rarely forms independent minerals in the crust but disperses as trace substitutions or minor sulfides (e.g., linnaéite, cobaltite) within polymetallic assemblages, limiting its primary dispersion to geochemical provinces enriched in iron-nickel-copper systems.[41]Major global deposits and reserves
The Democratic Republic of the Congo possesses the world's largest cobalt reserves, estimated at 6,000,000 metric tons, accounting for over half of the global total of 11,000,000 metric tons as of 2024.[45] These reserves are concentrated in sediment-hosted stratiform copper-cobalt deposits within the Katanga Copperbelt, particularly around major sites such as Kisanfu, Mutanda, and Tenke Fungurume, where cobalt occurs as a byproduct of copper mining in oxidized zones of sedimentary rock formations.[45] [46] Australia follows with 1,700,000 metric tons, primarily in nickel-cobalt laterite deposits in Western Australia, such as those at Murrin Murrin and Ravensthorpe, formed through supergene enrichment of ultramafic rocks.[45] Indonesia's reserves stand at 640,000 metric tons, largely in lateritic nickel-cobalt deposits on Sulawesi and other islands, associated with ophiolite complexes and intensified by recent exploration in high-pressure acid leach amenable ores.[45] Other significant reserves include Cuba's 500,000 metric tons in laterite profiles overlying serpentinized peridotites in eastern provinces like Moa Bay, and the Philippines' 260,000 metric tons in similar nickel laterites on non-volcanic islands.[45] Canada's 220,000 metric tons are mainly in magmatic nickel-copper sulfide deposits, such as those in the Sudbury Basin (Ontario) and Voisey's Bay (Labrador), where cobalt substitutes in pentlandite and pyrrhotite minerals.[45] Russia's 250,000 metric tons derive from Norilsk-Talnakh sulfide deposits in Siberia, linked to Siberian Traps magmatism, while smaller holdings like Madagascar's 100,000 metric tons occur in laterites and Zambia's contributions (included in "other countries" at 800,000 metric tons globally) stem from Copperbelt extensions.[45]| Country | Reserves (metric tons) |
|---|---|
| Congo (Kinshasa) | 6,000,000 |
| Australia | 1,700,000 |
| Indonesia | 640,000 |
| Cuba | 500,000 |
| Philippines | 260,000 |
| Russia | 250,000 |
| Canada | 220,000 |
| Other countries | 800,000 |
Production
Global production trends and statistics
Global cobalt mine production has expanded rapidly since the early 2010s, driven by surging demand for lithium-ion batteries in electric vehicles and consumer electronics, which now account for over half of total cobalt consumption. According to U.S. Geological Survey data, worldwide mine output increased from approximately 102,000 metric tons in 2010 to 164,000 metric tons in 2021, reflecting a compound annual growth rate exceeding 4%.[47][48] This growth accelerated further, with production reaching record highs of nearly 190,000 metric tons in 2022 and approximately 230,000 metric tons in 2023, primarily due to expanded mining in the Democratic Republic of the Congo and emerging output from Indonesian laterite deposits.[3][49] The Democratic Republic of the Congo dominates global supply, producing 74% of the world's cobalt in 2023, equivalent to about 170,000 metric tons, while Indonesia contributed around 10%, marking its rise as a key laterite-based producer.[50][51] Other contributors, including Australia, Canada, and Russia, accounted for the remainder, with diversified efforts in these nations aiming to mitigate supply risks from geopolitical instability in the DRC.[52] In 2024, mine production continued to set records, supported by operational expansions, while global refined cobalt output hit 222,000 metric tons, up 17% from 2023 levels, largely from increased Chinese processing capacity.[45][53]| Year | Global Mine Production (metric tons) | Key Driver |
|---|---|---|
| 2010 | 102,000 | Baseline industrial demand[47] |
| 2015 | ~130,000 | Early battery sector growth[3] |
| 2020 | 142,000 | Pandemic recovery and EV boom[54] |
| 2021 | 164,000 | DRC expansion[48] |
| 2023 | ~230,000 | Indonesia ramp-up and battery demand[49] |
| 2024 | Record high (est.) | Continued mine and refinery increases[45] |
Extraction techniques
Cobalt extraction primarily occurs as a by-product during the mining of copper, nickel, and other base metals, with dedicated cobalt mining limited to specific high-grade deposits. The process begins with ore extraction via open-pit or underground mining methods, selected based on deposit depth, grade, and geology; open-pit mining predominates for shallow, large-volume oxidized ores, while underground methods are used for deeper sulfide deposits to minimize overburden removal.[56][57] Ore beneficiation follows mining and involves crushing, grinding, and physical separation techniques such as froth flotation, gravity concentration, or magnetic separation to produce a cobalt-enriched concentrate. For sulfide ores, which constitute much of global supply alongside copper, flotation separates cobalt-bearing minerals like carrollite (CuCo2S4) or cobaltite (CoAsS) into a mixed Cu-Co sulfide concentrate, achieving recoveries of 80-90% under optimized conditions. Oxide ores, prevalent in regions like the Democratic Republic of Congo, often require less beneficiation due to their friable nature but may involve hand-sorting or simple screening in artisanal operations before chemical processing.[56][58][59] Hydrometallurgical methods dominate industrial cobalt recovery, involving acid leaching—typically with sulfuric acid under atmospheric or high-pressure conditions—to dissolve cobalt from concentrates or ores, followed by purification via solvent extraction and electrowinning. In the pressure acid leach (PAL) process for lateritic ores, ore is leached at 250°C and 40-60 bar, yielding cobalt recoveries exceeding 90%, though it demands significant energy for autoclave operation. For sulfide concentrates, roasting or bioleaching can precede sulfuric acid leaching to oxidize sulfides, with solvent extraction using organophosphorus reagents like Cyanex 272 to selectively separate cobalt from impurities such as copper, nickel, and iron. Pyrometallurgical routes, less common for cobalt due to high energy costs, include smelting to produce a matte from which cobalt is recovered via converting and leaching, often integrated with nickel processing.[59][60][61] Emerging techniques aim to improve efficiency and reduce environmental impact, such as bioleaching with acidophilic bacteria to extract cobalt from low-grade tailings, achieving up to 70% recovery in pilot tests without high-pressure equipment, or reductive leaching with sulfur dioxide gas for selective dissolution. These methods, however, remain secondary to established hydrometallurgical flowsheets, which account for over 70% of global cobalt production and are tailored to ore mineralogy—sulfides favoring roasting-leach-solvent extraction, and oxides direct leaching—to optimize yield while managing arsenic and other contaminants inherent in cobalt ores.[62][63][57]Key producing countries and methods
The Democratic Republic of the Congo (DRC) dominates global cobalt production, accounting for 74% of world mine output in 2023 with approximately 126,000 metric tons from a total of 170,000 metric tons.[3] Indonesia ranks second, contributing around 10% primarily through processing of nickel laterites, while Australia, Canada, Russia, and others make up the remainder, each under 5%.[51][3] These shares reflect cobalt's status as a by-product in most operations, tied to copper and nickel mining economics.[64] Extraction methods differ by ore type and regional geology. In the DRC, cobalt is recovered from oxidized copper-cobalt ores in the Katanga Copperbelt via open-pit and underground mining, followed by crushing, flotation for concentration, and hydrometallurgical processing such as solvent extraction and electrowinning to yield cobalt cathode or hydroxide precipitate.[64] Pyrometallurgical smelting is less common but used for some sulphide ores. Artisanal methods, involving manual digging and basic leaching, supplement industrial output but pose safety and environmental risks.[65] Indonesia's production centers on lateritic nickel-cobalt deposits in Sulawesi, processed via high-pressure acid leaching (HPAL) integrated with nickel solvent extraction, yielding mixed hydroxide precipitate (MHP) for battery precursors; this method has expanded rapidly since 2019 but faces technical challenges like tailings management.[53] In Australia, cobalt emerges as a by-product from nickel laterite and sulfide ores, treated through a mix of HPAL, atmospheric leaching, and bioleaching at operations like those in Western Australia.[64] Canada employs similar hydrometallurgical recovery from nickel-copper sulfides in Ontario's Sudbury Basin and other sites, often via pressure leaching.[64] Russia's output, from Norilsk Nickel, involves pyrometallurgical refining of nickel-copper mattes containing cobalt.[3]| Country | 2023 Production (metric tons) | Global Share (%) | Primary Ore Type and Method |
|---|---|---|---|
| Democratic Republic of the Congo | 126,000 | 74 | Copper-cobalt oxides; hydrometallurgy |
| Indonesia | 17,000 | 10 | Nickel laterites; HPAL |
| Australia | 5,000 | 3 | Nickel sulfides/laterites; leaching |
| Russia | 4,000 | 2.5 | Nickel-copper sulfides; pyrometallurgy |
| Canada | 3,500 | 2 | Nickel-copper sulfides; hydrometallurgy |
Democratic Republic of the Congo
The Democratic Republic of the Congo (DRC) dominates global cobalt production, supplying over 70% of the world's mined cobalt, with output estimated at 220,000 metric tons in 2024.[67][68] This production occurs primarily as a byproduct of copper mining in the Copperbelt region, spanning Lualaba and Haut-Katanga provinces, where oxide and sulfide ore deposits are processed via hydrometallurgical methods such as solvent extraction and electrowinning.[3][55] The sector's rapid expansion, driven by demand for lithium-ion batteries, has boosted DRC's economy, with mining contributing significantly to GDP growth of 6.5% in 2024, though it is marred by governance challenges, including export restrictions and ownership dominated by Chinese firms.[69][70]Industrial mining operations
Industrial-scale cobalt extraction in the DRC is concentrated in large copper-cobalt complexes operated by multinational corporations, including Glencore's Mutanda mine (producing around 20,000-30,000 tons of cobalt annually in recent years) and CMOC Group's Tenke Fungurume mine (output exceeding 40,000 tons in peak operations).[46] Other key sites include Kamoa-Kakula, managed by Ivanhoe Mines and Zijin Mining, and Kamoto Copper Company under Glencore, which together account for the bulk of the country's industrial output, estimated at 70-85% of total DRC cobalt.[71][72] These operations employ open-pit and underground methods, followed by ore concentration and leaching, with production ramping up due to global battery demand; for instance, Mutanda resumed full operations in 2021 after suspensions tied to low prices.[46] Chinese entities control a significant portion of these assets, influencing supply chains amid geopolitical tensions.[70]Artisanal and small-scale mining
Artisanal and small-scale mining (ASM) in the DRC historically contributed 10-30% of national cobalt output, with estimates of 12,000-18,000 tons from such sites in 2015-2016, though this share declined sharply to under 2% by 2024 due to low cobalt prices, regulatory crackdowns, and industrial encroachment.[73][74][75] ASM involves informal diggers using basic tools to extract high-grade oxide ores from shallow pits or tailings near industrial sites, often selling to intermediaries for processing; it employs 500,000 to 2 million people, providing livelihoods in impoverished areas but yielding inconsistent volumes amid market fluctuations.[76][71] Efforts to formalize ASM, such as zoning cooperatives and traceability pilots, have had limited success, with output integration into global supply chains complicating separation from industrial sources.[77]Labor conditions, child involvement, and ethical controversies
Labor conditions in DRC cobalt mining vary sharply: industrial operations adhere to international standards with mechanized safety measures, though reports document forced evictions and community displacements during expansions, as at Tenke Fungurume where thousands were affected without adequate compensation.[78] In contrast, ASM sites feature hazardous manual labor, including tunnel collapses and toxic dust exposure, with poverty compelling family involvement; child labor persists, affecting an estimated 40,000 children under 18 in cobalt ASM as of recent surveys, often for $1-2 daily wages to supplement household income.[79][80][81] Ethical controversies center on supply chain opacity, where ASM cobalt contaminates industrial streams, implicating downstream buyers like tech firms in child exploitation and fatalities—over 100 child deaths reported in mine accidents since 2019—despite audits and blockchain traceability initiatives by companies such as IBM and RCS Global.[82][83] Critics, including Amnesty International, argue that demand-driven growth exacerbates abuses without addressing root causes like extreme poverty, while proponents of industrial dominance note ASM's decline reduces risks but displaces workers into informal economies.[78][84][85]Industrial mining operations
Industrial cobalt mining in the Democratic Republic of the Congo (DRC) focuses on large-scale extraction primarily as a byproduct of copper production from oxide and sulfide ores in the Katangan Copperbelt, particularly in Lualaba and Haut-Katanga provinces. Operations utilize open-pit mining for oxide ores and underground methods for deeper sulfide deposits, followed by hydrometallurgical processing involving crushing, grinding, acid leaching, solvent extraction, and electrowinning to recover copper cathodes and cobalt hydroxide.[86][87] Glencore operates two major industrial assets: the Mutanda mine, an open-pit copper-cobalt operation in Lualaba Province, which produced 25,100 tonnes of cobalt hydroxide in 2019 before a temporary suspension, and the Kamoto Copper Company (KCC), a joint venture with Gécamines (Glencore 75%), encompassing open-pit mines at KOV and Mashamba East plus the underground KTO mine, recognized as the world's largest active cobalt mine as of 2022.[88][89] KCC processes ore at the Luilu metallurgical plant to yield copper cathodes and cobalt hydroxide.[88] Mutanda faced production cuts of up to 15% annually from 2023 due to depleting cobalt ore grades.[90] CMOC Group, holding an 80% stake in Tenke Fungurume Mining (TFM), manages one of the DRC's largest copper-cobalt complexes in Lualaba Province, employing open-pit methods and expanding with a $1.08 billion investment in the adjacent KFM mine announced in 2025 to boost output by approximately 100,000 metric tons of copper annually, alongside cobalt recovery.[87][91] TFM was the first African mine to receive The Copper Mark certification in 2024 for responsible practices.[92] These operations contributed to DRC's industrial cobalt output increase from 27,547 tonnes between 2015 and 2018, driven by expansions amid rising global demand, though challenges include infrastructure limitations and regulatory export quotas, such as allocations of 3,925 tonnes to KCC and 18,840 tonnes to Mutanda in 2025.[75][93] Chinese firms, including CMOC affiliates, control significant portions of DRC's industrial cobalt production capacity.[94]Artisanal and small-scale mining
Artisanal and small-scale mining (ASM) of cobalt in the Democratic Republic of the Congo (DRC) involves informal operations using basic tools to extract ore from surface deposits, underground tunnels, or industrial mine tailings. These activities are concentrated in the southeastern Copperbelt region, particularly around Kolwezi and Lubumbashi, where cobalt occurs in copper-cobalt ores like heterogenite and carrollite. Miners, often organized in cooperatives or individually, dig shallow pits or narrow shafts up to 30 meters deep without mechanization, then crush and wash ore manually to concentrate it for sale to intermediaries.[95] ASM has historically supplied 10-30% of DRC's cobalt output, equivalent to 5-15% of global production, but volumes fluctuate with cobalt prices and regulations; production peaked around 2008 at 40-53% of DRC totals before declining. In recent years, amid low prices and enforcement of mining codes restricting ASM on industrial concessions, artisanal output fell to less than 2% of DRC production by 2023, or roughly 3,000-4,000 metric tons annually from DRC's estimated 170,000-ton output. This represents about 1% of global cobalt mine production of approximately 200,000 tons. Estimates vary due to the sector's opacity, with informal sales often evading official tracking and ore smuggling to neighboring countries.[95][74][74] Operations pose severe hazards, including tunnel collapses killing dozens annually, exposure to toxic dust causing respiratory illnesses, and flooding risks in unregulated sites. Workers earn $1-2 per day, sifting ore for 12-hour shifts in unstable excavations lacking safety gear. An estimated 255,000 people engage in DRC cobalt ASM, with 40,000 children involved as of 2023, some as young as seven, performing dangerous tasks like hauling heavy loads underground. These conditions stem from poverty driving families to mining amid limited alternatives, compounded by weak enforcement of the 2018 Mining Code's child labor bans.[96][6][79] Efforts to formalize ASM include zoning designated areas away from industrial sites and traceability initiatives by buyers, but implementation lags due to corruption and artisanal encroachment on concessions. Environmental impacts involve acid mine drainage polluting waterways with heavy metals, though data on extent remains limited by underreporting. Despite ethical concerns raised by advocacy groups, which some industry sources view as exaggerated for leverage, the sector persists as a livelihood for marginalized communities, with cobalt from ASM entering global supply chains via refineries in China and elsewhere.[95]Labor conditions, child involvement, and ethical controversies
Artisanal and small-scale cobalt mining in the Democratic Republic of the Congo (DRC) involves hazardous working conditions, including manual excavation in unstable tunnels without protective equipment, exposure to toxic dust, and heavy physical labor in flooded or collapsing sites.[96] Miners often work 12- to 24-hour shifts for daily earnings of $1 to $2, with frequent injuries from rockfalls, machinery accidents, and chemical exposure leading to respiratory illnesses and skin conditions.[82] A 2024 U.S. Department of Labor report on forced labor documented widespread indicators such as debt bondage, withheld wages, and threats of violence among cobalt workers, affecting nearly all in the sector.[6] Child labor is prevalent, with estimates indicating at least 25,000 children engaged in cobalt mining across the DRC as of 2025, many as young as seven years old performing tasks like digging narrow tunnels and carrying ore sacks weighing up to 50 kilograms.[97] These children face heightened risks of fatal accidents, such as tunnel collapses that have killed or maimed dozens annually, and long-term health issues from inhaling cobalt-laden dust without masks or ventilation.[80] Government and NGO efforts, including a pilot Child Labor Monitoring and Remediation System in 10 sites that identified and addressed cases involving 5,346 children by December 2023, have had limited impact due to poverty driving families to mining for survival.[98] Ethical controversies center on the global supply chain, where artisanal cobalt—comprising 15-20% of DRC's output—enters industrial streams with minimal traceability, implicating battery manufacturers and tech firms in child exploitation.[99] A 2019 U.S. lawsuit accused companies like Apple, Google, Dell, Microsoft, and Tesla of benefiting from child labor after two miners under 18 died in landslides, highlighting failures in due diligence despite industry audits.[100] Chinese firms control about 80% of DRC cobalt production, often blending artisanal ore into exports, which critics argue enables forced labor propagation despite international pressure for ethical sourcing.[101] A 2025 University of Nottingham report found the majority of artisanal miners trapped in forced labor conditions, underscoring systemic abuses amid rising demand for electric vehicle batteries.[102]Other major producers
Indonesia emerged as the second-largest cobalt producer in 2024, with output reaching 28,000 metric tons (MT), primarily from nickel-cobalt laterite deposits processed via high-pressure acid leaching (HPAL).[67] These operations, concentrated in Sulawesi and Halmahera, are dominated by Chinese firms like Tsingshan Holding Group and Zhejiang Huayou Cobalt, leveraging Indonesia's vast nickel laterite reserves—estimated at over 21 million MT of cobalt content—to supply battery-grade intermediates.[67] Production surged 937% since 2017, driven by downstream integration into electric vehicle battery manufacturing, though environmental concerns from tailings and deforestation have prompted regulatory scrutiny.[67]Indonesia and laterite deposits
Cobalt production in Indonesia relies almost exclusively on lateritic ores, formed from weathered ultramafic rocks rich in nickel and cobalt, unlike the sedimentary copper-cobalt deposits dominant in the DRC.[3] Key projects include the Morowali Industrial Park and Weda Bay Industrial Park, where HPAL facilities recover cobalt hydroxide alongside nickel sulfate, with capacities exceeding 100,000 MT of nickel annually and co-product cobalt yields of several thousand MT.[53] In 2024, these methods accounted for over 90% of Indonesia's cobalt output, benefiting from government bans on raw nickel ore exports since 2020 that spurred domestic refining.[67] However, HPAL processes are energy-intensive and technically challenging, with recovery rates for cobalt typically 80-90%, and acid consumption posing scalability issues amid fluctuating ore grades averaging 0.1-0.2% cobalt.[3]Australia, Canada, and diversification efforts
Australia produced approximately 4,800 MT of cobalt in 2023, mainly from the Murrin Murrin operation in Western Australia, a laterite mine operated by Glencore that yields cobalt as a nickel by-product via HPAL and solvent extraction.[3] The Symon Mine, also by Glencore, contributes additional output from similar deposits. Canada's production stood at around 3,300 MT in 2023, primarily from Vale's Voisey's Bay mine in Labrador, extracting cobalt from nickel-copper sulfide ores, with emerging projects like Fortune Minerals' NICO deposit targeting refractory ore processing for 1,300 MT annual capacity by 2027.[64] These countries represent diversification priorities for Western nations, with Australia and Canada holding combined reserves of over 1.5 million MT and benefiting from stable governance and environmental standards.[103] Efforts to expand non-DRC supply include government-backed initiatives, such as Australia's Critical Minerals Strategy allocating AUD 1.25 billion for downstream processing and Canada's CAD 3.8 billion Critical Minerals Strategy funding exploration and refining to reduce reliance on Chinese-dominated supply chains controlling 70% of global cobalt refining.[64] Projects like IGO's Nova-Bollinger expansion and Cobalt 27's North American refinery aim to boost output by 5,000-10,000 MT combined by 2026, emphasizing ethical sourcing and recycling to mitigate geopolitical risks from DRC instability and Indonesian export controls.[45] Russia, with 8,700 MT in 2024 from Norilsk Nickel's sulfide operations in Siberia, remains a notable producer but faces sanctions limiting Western market access.[67]Indonesia and laterite deposits
Indonesia's cobalt production derives primarily from laterite deposits rich in nickel-cobalt ores, concentrated in regions such as Sulawesi, Maluku, and West Papua.[104] These saprolitic and limonitic laterites form through weathering of ultramafic rocks, yielding lower cobalt grades compared to sedimentary copper-cobalt ores but enabling large-scale open-pit extraction.[105] In 2023, Indonesia accounted for 8% of global cobalt mine production, ranking second behind the Democratic Republic of the Congo, with output estimated at 17,000 metric tons.[106] Production rose to 28,000 metric tons in 2024, driven by expansions in nickel processing facilities that recover cobalt as a byproduct.[67] Key projects include the Weda Bay Industrial Park on Halmahera Island, operated by Tsingshan Holding Group and partners, which processes laterite ores via high-pressure acid leaching (HPAL) to produce mixed nickel-cobalt hydroxide precipitate (MHP).[107] The PT Halmahera Persada Lygend (HPL) project, a joint venture involving Chinese firm Lygend Resources, features multiple HPAL lines with a combined cobalt capacity exceeding 14,000 metric tons annually from processing over 3 million tons of laterite ore per phase.[108] Other notable operations, such as the Huayue Nickel Cobalt HPAL facility where Nickel Industries holds a stake, focus on battery-grade outputs from low-carbon processing of domestic laterites.[109] HPAL technology dominates laterite processing in Indonesia, involving sulfuric acid leaching under high temperature and pressure to selectively extract nickel and cobalt, followed by precipitation into MHP for downstream refining.[110] A 2020 export ban on raw nickel ores compelled investment in domestic smelting and hydrometallurgical plants, boosting cobalt recovery rates despite challenges like high capital costs and environmental tailings management.[111] By early 2024, tracked HPAL projects had expanded rapidly, with Indonesia poised to supply 16% of global cobalt by 2030 through nickel-cobalt integrations.[110] Chinese firms control much of the investment and output, leveraging Indonesia's 21 million tons of nickel reserves—20.6% of the global total—which co-occur with cobalt.[112]Australia, Canada, and diversification efforts
Australia's cobalt production primarily derives from nickel-cobalt laterite deposits, with major operations including Glencore's Murrin Murrin mine in Western Australia, which processes ore through high-pressure acid leaching to recover cobalt as a hydroxide byproduct.[113] In 2024, national output reached 5.33 thousand tonnes, representing approximately 1-2% of global supply despite holding the world's second-largest reserves at 1.7 million metric tons.[114][115] Queensland accounts for about 14% of Australia's resources, supporting exploration and development amid efforts to expand dedicated cobalt projects like Cobalt Blue's Broken Hill initiative.[116][117] Canada produces cobalt mainly as a byproduct of nickel-copper sulfide mining, with key sites such as Vale's Voisey's Bay in Newfoundland and Labrador and Glencore's Sudbury operations in Ontario.[118] In 2023, output exceeded 5,000 tonnes, with Newfoundland and Labrador contributing 43% (2,188 tonnes) and the remainder from Ontario, Manitoba, and Quebec.[64][119] Production is projected to grow at a 7% CAGR through 2027, driven by expansions in these established sulfide deposits.[118] Diversification initiatives emphasize Australia and Canada as stable alternatives to DRC dominance, leveraging their regulatory frameworks and technological capabilities for ethical, low-risk supply chains.[120] The US-Australia Critical Minerals Partnership, valued at $8.5 billion as of 2025, targets end-to-end cobalt processing to reduce import dependencies, while tripartite efforts with Canada under the Critical Minerals Mapping Initiative aim to map and develop North American-Australasian resources.[121][122] In Canada, a $20 million US Department of Defense grant in 2024 supports Ontario's first cobalt sulfate refinery, enhancing refining independence from overseas processors.[123] These strategies, including waste stream recovery projects spanning both nations, prioritize advanced mining techniques over artisanal methods to secure battery-grade cobalt for electric vehicles and renewables.[124][125]Applications
Alloys and high-performance materials
Cobalt-based superalloys are utilized in gas turbine components, including turbine blades and engine parts, to provide elevated temperature strength exceeding 1000°C, along with resistance to oxidation and hot corrosion.[126] These alloys typically comprise 35% to 70% cobalt, with additions of chromium, nickel, and other elements to form stable microstructures under extreme thermal loads.[127] In aviation applications, such as jet engines produced by manufacturers like Rolls-Royce and Pratt & Whitney, cobalt enhances high-temperature stability, corrosion resistance, and wear performance, enabling efficient operation in demanding environments.[128][129] Superalloys represent the primary use of cobalt in the United States, consuming over 90% of the metal in aircraft engine production as of 1980, with demand driven by the need for materials that resist creep and fatigue.[130] Wear-resistant cobalt alloys, such as the Stellite family, consist of cobalt-chromium matrices with carbide formers like tungsten and molybdenum, offering superior resistance to abrasion, erosion, galling, and cavitation.[131] Stellite 6, for instance, maintains hardness and integrity up to 600°C, making it suitable for hardfacing on cutting tools, valves, and pump components exposed to corrosive slurries or high-velocity flows.[132] These alloys' performance stems from the formation of hard chromium-rich carbides dispersed in a tough cobalt matrix, which provides five to ten times the wear life of steel in abrasive conditions.[133] In permanent magnets, samarium-cobalt (SmCo) alloys deliver high coercivity and energy product, with operational temperatures up to 350°C and inherent corrosion resistance without coatings, ideal for motors in aerospace and military systems.[134] Alnico magnets, combining aluminum, nickel, iron, and 20-30% cobalt, exhibit directional magnetism and thermal stability up to 525°C, used in sensors and actuators where demagnetization resistance is critical.[135] Cobalt-chromium-molybdenum (CoCrMo) alloys are applied in medical implants, such as hip and knee prostheses, due to their biocompatibility, fatigue strength, and low wear rates in articulating joints.[136] These materials form passive oxide layers that minimize ion release and support long-term osseointegration, with clinical data showing reduced revision rates compared to alternatives in load-bearing applications.[137]Batteries and energy storage
Cobalt serves primarily as a component in the cathodes of lithium-ion batteries, where it enhances structural stability, electronic conductivity, and volumetric energy density in layered oxide materials such as lithium cobalt oxide (LiCoO₂) and nickel-manganese-cobalt oxides (NMC).[138][139] In these cathodes, cobalt compensates for charge variations during lithium-ion intercalation and deintercalation, mitigating phase transitions that could degrade performance.[140] High-nickel variants like NMC 811 incorporate approximately 10% cobalt by molar ratio to suppress cation mixing and preserve layered integrity during cycling.[141] In electric vehicle (EV) batteries, NMC and nickel-cobalt-aluminum (NCA) cathodes dominate high-energy-density applications, with cobalt enabling higher specific capacities compared to cobalt-free alternatives like lithium iron phosphate (LFP).[142] LFP batteries, which omit cobalt, offer lower energy density (typically 160-180 Wh/kg versus 200-250 Wh/kg for NMC) but greater thermal stability and cost advantages, prompting a shift in some EV models and nearly all stationary energy storage.[143][144] Despite this, cobalt-containing cathodes persist in premium EVs for their superior range and power output, with cobalt comprising 5-15% of cathode mass depending on the NMC ratio.[145] Global cobalt demand from batteries reached significant levels in 2024, driven by EV adoption and grid storage expansion, accounting for over 70% of total consumption; energy storage systems alone saw battery demand rise 56% year-over-year.[53] Projections indicate a 4% increase in overall cobalt demand for 2025 and 6% for 2026, tempered by ongoing cathode innovations aiming to reduce cobalt content to below 5% in high-nickel formulations while maintaining cycle life.[146] For grid-scale energy storage, the pivot to LFP has diminished cobalt reliance, as these systems prioritize longevity and safety over density, though cobalt-enhanced batteries remain viable for high-power applications requiring rapid discharge.[147][148] Efforts to eliminate cobalt entirely face challenges in preserving energy density and stability, with empirical data showing cobalt's role in extending cycle life by 30-40% in demanding conditions.[149]Catalysts, pigments, and radioisotopes
Cobalt compounds, particularly cobalt oxides and sulfides, function as heterogeneous catalysts in petroleum refining processes, notably in hydrodesulfurization (HDS) where cobalt-molybdenum catalysts remove sulfur impurities from fuels to meet environmental regulations.[150] These catalysts operate under high-pressure hydrogen atmospheres, promoting the conversion of organosulfur compounds into hydrogen sulfide, with cobalt enhancing the active sites' selectivity and stability compared to molybdenum alone.[150] Cobalt-based catalysts also find application in the Fischer-Tropsch synthesis for producing synthetic hydrocarbons from syngas, though iron catalysts dominate larger-scale operations due to cost factors.[151] Emerging uses include cobalt spinel oxides (Co3O4) for oxygen evolution reactions in water electrolysis for hydrogen production, valued for their electrochemical stability but challenged by overpotential issues in acidic media.[152] Cobalt pigments, primarily derived from cobalt(II) aluminate (CoAl2O4) or cobalt oxide (CoO), impart intense blue hues to ceramics, glass, and paints due to their thermal and chemical stability.[153] In ceramics, cobalt oxide is incorporated into glazes or underglazes for durable decoration, resisting leaching and fading under high firing temperatures up to 1300°C, as seen in historical applications like 14th-century Chinese blue-and-white porcelain.[154] For glassmaking, small additions of 0.1-1% cobalt oxide yield deep blue colors via d-d electron transitions in octahedral Co²⁺ ions, historically used since ancient Mesopotamian times for perfume bottles and later in European stained glass.[155] Modern formulations extend to artists' pigments in oils, acrylics, and watercolors, though high toxicity limits raw cobalt use, prompting substitutions with less vibrant alternatives amid supply concerns.[156] Cobalt-60 (²⁶⁰Co), a beta and gamma emitter with a half-life of 5.27 years, serves as a high-intensity radiation source in medical radiotherapy, delivering gamma rays at 1.17 and 1.33 MeV to target deep-seated tumors in teletherapy units.[19] Its primary non-medical application is sterilizing single-use medical devices like syringes, gloves, and implants via gamma irradiation, which penetrates packaging to eliminate bacteria without heat damage, accounting for over 50% of global Co-60 demand.[157] Industrial uses include nondestructive testing via radiography to detect welds and material flaws, as well as density gauges and thickness control in manufacturing.[19] Cobalt-57 (²⁷Co), with a shorter half-life of 271 days, supports nuclear medicine imaging as a tracer in vitamin B12 absorption studies and positron emission tomography precursors, though its production remains limited compared to Co-60.[158] Production of these isotopes occurs via neutron activation of stable cobalt-59 in nuclear reactors, with Canada supplying about 75% of global Co-60 as of 2023.[159]Emerging and niche uses
Cobalt-chromium alloys, prized for their biocompatibility, wear resistance, and mechanical durability, are employed in orthopedic implants including hip, knee, and spinal replacements, as well as dental prosthetics and surgical instruments. These alloys, typically comprising 60-65% cobalt with additions of chromium and molybdenum, enable long-term implantation by resisting corrosion in physiological environments and maintaining structural integrity under load.[160] [161] Such applications leverage cobalt's historical track record in load-bearing medical devices, though device-specific performance varies based on alloy composition and manufacturing.[162] In additive manufacturing, cobalt-chrome superalloys serve as feedstock powders for direct metal laser sintering (DMLS) and selective laser melting (SLM), facilitating the production of intricate, high-strength components for aerospace turbines and customized medical implants. These materials exhibit excellent creep resistance at elevated temperatures and a favorable strength-to-weight ratio, enabling lightweight designs unattainable via traditional casting.[163] [164] Adoption has grown with advancements in 3D printing precision, supporting rapid prototyping and on-demand fabrication in sectors demanding corrosion-resistant, biocompatible parts.[165] Emerging catalytic roles position cobalt as a non-precious metal alternative in green hydrogen production, particularly through electrocatalysts for water splitting and hydrogen evolution reactions. Cobalt complexes and nanoparticles demonstrate high activity in acidic or neutral media, with recent formulations achieving stability against deactivation for sustained electrolysis.[166] [167] Bimetallic cobalt systems, such as nickel-cobalt hybrids, enable lower-temperature hydrogen release from ammonia borane, enhancing efficiency in decentralized energy applications.[168] These developments, driven by cobalt's abundance relative to platinum-group metals, support scalable renewable hydrogen pathways amid net-zero transitions.[169]Economic and Geopolitical Significance
Market dynamics, pricing, and supply chains
Global cobalt demand reached approximately 139,000 metric tons in 2024, driven primarily by lithium-ion battery applications, which accounted for over 70% of consumption, with electric vehicle production as the key end-use.[170] Supply exceeded demand in 2024, leading to market oversupply estimated at around 20,000-30,000 tons, influenced by increased output from the Democratic Republic of Congo (DRC), which produced 74% of global mined cobalt, and rising contributions from Indonesia's nickel laterite processing.[3] This imbalance stemmed from slower-than-expected battery demand growth amid economic headwinds in EV markets, though projections indicate demand surpassing 210,000 tons by 2025 as battery chemistries stabilize and EV adoption accelerates.[171] Cobalt prices exhibited volatility, plummeting to lows around $24,000 per metric ton in late 2023 before surging early in 2025 to over $32,500 per metric ton in Q2, reflecting supply disruptions and speculative trading.[172] By October 2025, spot prices hovered near $33,482 per metric ton in the US, up from $24,080 a year prior, buoyed by anticipated demand recovery and easing oversupply.[173] Forecasts suggest an average of 10.98 per pound) for 2025, lower than 2024's $29,000 equivalent but signaling stabilization as supply growth moderates to 5-8% annually while demand grows at 8-10%.[174] Price sensitivity arises from the metal's role in nickel-manganese-cobalt (NMC) cathodes, where substitution efforts toward lower-cobalt formulas have tempered but not eliminated reliance. The cobalt supply chain begins with mining, predominantly as a byproduct of copper and nickel extraction: in the DRC from sedimentary copper deposits yielding cobalt hydroxide intermediates, and in Indonesia from lateritic nickel ores processed via high-pressure acid leaching (HPAL).[175] Refining, which converts intermediates to battery-grade chemicals like cobalt sulfate, is highly concentrated, with over 70% of capacity in China as of 2023, creating chokepoints vulnerable to export restrictions and processing bottlenecks.[176] Downstream, refined cobalt feeds into cathode production (primarily in Asia) and alloy manufacturing, with recycling recovering only 10-15% of supply, mostly from spent batteries and superalloys, limiting circularity due to collection inefficiencies.[177] Geopolitical risks amplify chain fragility, as DRC instability and Chinese refining dominance expose markets to disruptions, prompting Western efforts to onshore processing despite higher costs.[178]China's dominance and Western diversification strategies
China controls approximately 65-75% of global cobalt refining capacity, processing the majority of output from the Democratic Republic of the Congo (DRC), which accounted for 74% of worldwide mine production in 2024.[3] [179] Chinese firms hold ownership stakes in about 80% of DRC cobalt mines, enabling vertical integration from extraction to battery-grade chemicals, while exporting 66% of global unwrought cobalt by value in 2024.[180] [181] This dominance stems from state-backed investments since the early 2000s, including infrastructure-for-minerals deals in the DRC, which have secured long-term supply amid rising electric vehicle demand.[179] Western nations, facing supply vulnerabilities exposed by price volatility—such as cobalt's 59.5% decline from $82,000 per ton in May 2022 to $33,250 per ton in May 2025—have pursued diversification through policy incentives and international partnerships, including establishing national strategic reserves. Cobalt's status as a key battery mineral, combined with supply concentration in the DRC (accompanied by ethical concerns in mining practices) and refining dominance by China, positions it as a candidate for such reserves by countries like the US and China to mitigate risks.[182][183] The United States, via the Inflation Reduction Act of 2022 and Bipartisan Infrastructure Law, allocated billions for domestic processing facilities, including grants to projects like Jervois Global's Idaho cobalt operations, aiming to reduce reliance on Chinese refineries that handle over 60% of global supply.[53] [184] European efforts center on the Critical Raw Materials Act (2024), which targets 10% domestic extraction and 40% processing capacity by 2030, fostering joint ventures in Australia and Canada for non-Chinese laterite deposits and nickel-cobalt projects.[185] [186] Allies like Australia have expanded output, with 2024 production reaching significant levels through mines such as Glencore's Murrin Murrin, supported by U.S. and EU offtake agreements to bypass Chinese intermediaries.[67] Canada similarly advances sulfide deposits in Ontario and Quebec, backed by federal subsidies exceeding CAD 1 billion since 2023 for refining independence.[187] These strategies emphasize allied supply chains, though challenges persist due to higher Western production costs and China's alleged market flooding tactics.[188]Recycling advancements and future supply security
Global cobalt recycling remains limited, with end-of-life recycling rates estimated at around 16% for batteries and portable electronics, resulting in significant losses such as over 34,000 tonnes of cobalt in e-waste in 2022, equivalent to one-sixth of annual global supply.[189][190] Advancements in hydrometallurgical processes have improved recovery efficiency, achieving up to 95% for cobalt from lithium-ion batteries while reducing greenhouse gas emissions by 80% compared to primary mining.[191][192] Companies like Apple have committed to using 100% recycled cobalt in batteries by 2025, driven by supply chain diversification goals.[193] The cobalt recycling market, valued at USD 1.443 billion in 2024, is projected to grow to USD 1.587 billion in 2025 and reach USD 3.479 billion by an unspecified later date, fueled by rising electric vehicle battery end-of-life volumes and regulatory mandates such as the EU Battery Regulation requiring 90% cobalt recovery by 2027 and 95% by 2031.[194][195] Pyrometallurgical and advanced hydrometallurgical technologies are enhancing material purity and yield, though challenges persist, including low collection rates below 15% in regions like the United States and technical difficulties in separating cobalt from complex alloys or degraded cathodes, which limit overall efficiency.[196][197][198] For future supply security, battery recycling could supply 20-30% of cobalt demand by mid-century under scenarios with improved collection, potentially increasing global supply by 23% and reducing prices by 60% by 2030 if EU regulations are fully implemented, thereby mitigating risks from concentrated mining in the Democratic Republic of Congo.[199][200] Combined efficiency gains and recycling may lower primary cobalt requirements by up to 75% through 2050, supporting energy transition goals without fully resolving short-term deficits projected at 50% for cobalt over the next decade absent accelerated low-cobalt cathode adoption.[201][202] However, geopolitical vulnerabilities, including China's dominance in processing over 65% of recycled battery minerals, underscore the need for Western investments in domestic facilities to enhance strategic autonomy.[203]Biological Role
Essential functions in organisms
Cobalt functions primarily as the central metal ion in the corrin ring of cobalamin (vitamin B12), the only known biologically active organometallic compound containing cobalt-carbon bonds. In humans and other mammals, cobalamin serves as a cofactor for two enzymes essential to metabolic processes: methionine synthase, which catalyzes the transfer of a methyl group from 5-methyltetrahydrofolate to homocysteine, producing methionine and tetrahydrofolate for DNA synthesis and epigenetic regulation; and methylmalonyl-CoA mutase, which isomerizes methylmalonyl-CoA derived from propionate, isoleucine, valine, methionine, threonine, and odd-chain fatty acids into succinyl-CoA for entry into the tricarboxylic acid cycle. These reactions support red blood cell formation, myelin sheath maintenance, and fatty acid oxidation, with daily human requirements met through microgram-level dietary intake via B12 absorption in the ileum.[204][205][206] In ruminants such as cattle and sheep, cobalt's role is indirect but critical, as rumen bacteria synthesize cobalamin de novo using dietary cobalt, which is then absorbed by the host animal for the same enzymatic functions; deficiency disrupts propionate utilization, leading to impaired energy metabolism and weight loss. Non-ruminant animals rely on exogenous B12 from animal-derived foods or microbial sources, underscoring cobalt's indispensability across vertebrate metabolism.[207][208] Among microorganisms, cobalt enables cobalamin-dependent enzymes in bacteria, archaea, and certain algae, facilitating reactions like ribonucleotide reduction, glycerol dehydration, and carbon skeleton rearrangements in anaerobic pathways such as methanogenesis in Methanosarcina species and acetogenesis in Acetobacterium genera. Prokaryotes capable of B12 biosynthesis, including those in the gut microbiome, incorporate cobalt to sustain these redox-active processes, which are absent in higher plants where cobalt exhibits no established essentiality despite occasional benefits to symbiotic nitrogen-fixing bacteria in legumes.[205][209]Deficiency symptoms and dietary sources
Cobalt serves an essential role in human biology solely as the central metal ion in vitamin B12 (cobalamin), a coenzyme critical for DNA synthesis, red blood cell maturation, and myelin sheath maintenance in the nervous system.[206][204] Humans cannot synthesize vitamin B12 and rely on dietary intake, where cobalt deficiency manifests indirectly through insufficient bioavailable B12, rather than free cobalt ions, which the body does not utilize directly.[206] Isolated cobalt deficiency apart from B12 shortfall is exceedingly rare in humans due to the element's incorporation exclusively into this vitamin form.[205] Symptoms of cobalt-related deficiency align with those of vitamin B12 depletion and typically develop gradually over years, as body stores (primarily in the liver) can last 2–5 years in adults.[210] Early signs include fatigue, weakness, pallor, and shortness of breath from megaloblastic anemia, characterized by enlarged, immature red blood cells impairing oxygen transport.[211][212] Neurological manifestations, stemming from demyelination, encompass paresthesia (tingling or numbness in extremities), ataxia (impaired coordination), diminished reflexes, memory loss, cognitive impairment, mood swings, and glossitis (inflamed tongue).[210][211][213] Untreated progression can yield irreversible neuropathy, subacute combined degeneration of the spinal cord, and increased homocysteine levels elevating cardiovascular risk.[210] Populations at elevated risk include vegans without supplementation, elderly individuals with atrophic gastritis reducing absorption, and those with pernicious anemia (autoimmune intrinsic factor deficiency) or ileal resection impairing B12 uptake.[214][212] Dietary cobalt intake occurs primarily via vitamin B12-containing foods, with average daily absorption supplying 1–3 μg of B12 (equating to trace cobalt quantities) in omnivorous diets.[205] Animal products dominate as sources, as B12 is synthesized by bacteria in ruminant guts or marine environments and accumulates in tissues:- Organ meats: Liver (e.g., beef liver provides ~70 μg B12/100 g) and kidneys offer the highest concentrations.[215]
- Meat and poultry: Beef, pork, and chicken (~2–5 μg B12/100 g).[216]
- Fish and shellfish: Salmon, tuna, oysters, and clams (up to 80–100 μg B12/100 g in mollusks).[217][215]
- Dairy and eggs: Milk, cheese, and eggs (~0.5–1 μg B12/serving).[212][216]

