Cobalt CAS 7440-48-4

Introduction:Basic information about Cobalt CAS 7440-48-4, including its chemical name, molecular formula, synonyms, physicochemical properties, and safety information, etc.

Cobalt Basic informationChemical Properties Physical properties Discovery History Uses Production Methods

Product Name:Cobalt
Synonyms:Cobalt, plasma standard solution, Co 10μg/mL;Cobalt wire, 0.1mm (0.004 in.) dia.;Cobalt wire, 0.25mm (0.01 in.) dia.;Cobalt slug, 3.175mm (0.125 in.) dia. x 3.175mm (0.125 in.) length;Cobalt rod, 12mm (0.47 in.) dia.;Cobalt sputtering target, 50.8mm (2.0 in.) dia. x 3.18mm (0.125 in.) thick;Cobalt sputtering target, 76.2mm (3.0 in.) dia. x 6.35mm (0.250 in.) thick;Cobalt foil, 0.127mm (0.005 in.) thick, 50x50mm (2x2 in.)
CAS:7440-48-4
MF:Co
MW:58.93
EINECS:231-158-0
Product Categories:metal or element;nano structured metal;Metals;Inorganics;Catalysis and Inorganic Chemistry;Chemical Synthesis;Cobalt;Metal and Ceramic Science;CobaltMetal and Ceramic Science;C-D, Puriss p.a.Chemical Synthesis;Analytical Reagents for General Use;Puriss p.a.
Mol File:7440-48-4.mol

Cobalt Chemical Properties

Melting point 1495°C
Boiling point 2900 °C (lit.)
bulk density850kg/m3
density 8.9 g/mL at 25 °C (lit.)
vapor pressure 0Pa at 20℃
storage temp. no restrictions.
solubility H2O: soluble
form wire
color Pink to red to violet
Specific Gravity8.9
Flame ColorSilvery white
resistivity6.24 μΩ-cm, 20°C
Water Solubility insoluble
Merck 13,2452
Exposure limitsTLV-TWA 0.05 mg as Co/m3 (ACGIH)
PEL-TWA: 0.05 mg as Co/m3 (NIOSH,OSHA)
TLV-STEL 0.1 mg as Co/m3 (ACGIH)
IDLH 20 mg as Co/m3 (NIOSH)
.
Stability:Stable, but pyrophoric in air when finely divided. Incompatible with acetylene, hydrazinium nitrate, oxidizing agents, acids.
InChI1S/Co
InChIKeyGUTLYIVDDKVIGB-UHFFFAOYSA-N
SMILES[Co]
Shear Modulus82.6 GPa
Poissons Ratio0.32
Modulus of Elasticity211 GPa
Hardness, Brinell125
Hardness, Vickers253
CAS DataBase Reference7440-48-4(CAS DataBase Reference)
IARC2B (Vol. 52) 1991, 2B (Vol. 86) 2006, 2A (Vol. 86) 2006
NIST Chemistry ReferenceCobalt(7440-48-4)
EPA Substance Registry SystemCobalt (7440-48-4)

Safety Information

Hazard Codes T,Xn,F
Risk Statements 45-23/24/25-34-53-42/43-40-36/37-36/38-17-11-15
Safety Statements 53-23-26-36/37/39-45-61-37-24-22-36/37-5-43
OEBD
OELTWA: 0.05 mg/m3
RIDADR UN 3264 8/PG 3
WGK Germany 3
RTECS GF8750000
TSCA TSCA listed
HS Code 8105 20 00
HazardClass 4.1
PackingGroup III
Storage Class4.1B - Flammable solid hazardous materials
Hazard ClassificationsAquatic Chronic 4
Carc. 1B
Eye Irrit. 2
Flam. Sol. 1
Muta. 2
Repr. 1B
Resp. Sens. 1
Skin Sens. 1
Hazardous Substances Data7440-48-4(Hazardous Substances Data)
ToxicityLD50 orally in Rabbit: 6170 mg/kg
IDLA20 mg Co/m3

Cobalt Usage And Synthesis

Chemical PropertiesCobalt is a silvery-gray brittle but hard metal, which is distributed widely in nature, including rocks, soil, plants, and animals. It is a metal with no odor and no vapor pressure at room temperature and is insoluble in water, except for ultrafine cobalt powder, which is water soluble. It is stable in air but chemically reactive with dilute acids and is a nonvolatile metal. Required in small amounts, cobalt is important for the sustenance of life. It is the only metal found in vitamins, most importantly as a part of vitamin B12 and is necessary in the formation of blood. Cobalt is a component of many naturally occurring minerals like sulfides, hydrates, and oxides. Cobalt compounds can occur in various oxidation states (0, +1, +2, +3, and +4) but the most common oxidation states are +2 and +3. Cobalt has one naturally occurring isotope, cobalt-59 and 26 radioactive isotopes.

Cobalt and its compounds are used as an important catalyst in various industrial processes. Cobalt catalysts are used in various processes such as a desulfurization catalyst for gas and oil and for polyesters, pottery, plastic, and detergent production. Cobalt is usually recovered as a byproduct of mining and refining of various minerals like copper and iron. It has the unique ability to be ductile as well as a malleable metal. This property allows it to be transformed into both thin wires and thin sheets.
Physical propertiesCobalt is a hard magnetic metal, like iron and nickel. It has the properties of both ductility as well as malleability. Due to this property, it can be molded into wires and compressed into sheets. Cobalt occurs in two allotropic forms, hexagonal and cubic. The hexagonal form is more stable than the cubic form at room temperature. The boiling point of cobalt is about 2927 °C (5301°F) and the melting point is about 1490 °C (2723°F). Cobalt as a metal is mildly reactive with oxygen and will burn only in powder form. It is soluble in dilute acids but is water soluble only in ultrafine powder form (Kyono et al., 1992).
DiscoveryCobalt(Co) is a metallic chemical element, specifically number 27 on the Periodic Table of the Elements. Cobalt was first discovered by George Brandt in 1739, a Swedish chemist, but it was not until 1780 that cobalt was confirmed as an element by Torbern Bergman. Cobalt has a long history of being mined, from which its name is a relic. Cobalt is derived from the German word kobold, which translates into“goblin”or “evil spirit,”as it was obtained as a byproduct of silver mining in Germany. When the cobalt-containing ore was smelted to isolate the silver, toxic arsenic-trioxide (AsO3) gas was released, which the miners attributed to the cobalt rather than the arsenic contained in the ore. Despite its inauspicious beginnings, cobalt has become an integral part of our technologically advanced world.
HistoryThe metal was isolated by Brandt in 1735 and confirmed as an element by Bergman in 1780. Cobalt is widely distributed in nature, but in small concentrations. Its concentration in the earth’s crust is estimated to be about 0.0025% and in the sea water is about 0.02 µg/L.Most cobalt found on earth is diffused into the rocks. It also is found in coal and soils, and at trace concentations in animals and plants. It is an essential element for plants and animals (as vitamin B12). Its absence in animals can cause retarded growth, anemia and loss of apetite. The element has been detected in meteorites and in the atmospheres of the sun and other stars.
UsesCobalt has been in use as a coloring agent for glass since ancient times. The most imporant use of cobalt is in the manufacture of various wearresistant and superalloys. Its alloys have shown high resistance to corrosion and oxidation at high temperatures. They are used in machine components. Also, certain alloys are used in desulfurization and liquefaction of coal and hydrocracking of crude oil shale. Cobalt catalysts are used in many industrial processes. Several cobalt salts have wide commercial applications Cobalt oxide is used in glass to impart pink or blue color. Radioactive cobalt–60 is used in radiography and sterilization of food.
Production MethodsCobalt is obtained from its ores, which are mostly sulfide, arsenic sulfide or oxide in nature. The finely ground ore is subjected to multistep processing, depending on the chemical nature of the ore.
When the sulfide ore carrollite, CuS•Co2S3, is the starting material, first sulfides are separated by flotation with frothers. Various flotation processes are applied. The products are then treated with dilute sulfuric acid producing a solution known as copper-cobalt concentrate. This solution is then electrolyzed to remove copper. After the removal of copper, the solution is treated with calcium hydroxide to precipitate cobalt as hydroxide. Cobalt hydroxide is filtered out and separated from other impurities. Pure cobalt hydroxide then is dissolved in sulfuric acid and the solution is again electrolyzed. Electrolysis deposits metallic cobalt on the cathode.
Production of cobalt in general is based on various physical and chemical processes that include magnetic separation (for arsenic sufide ores), sulfatizing roasting (for sulfide ores), ammoniacal leaching, catalytic reduction, and electrolysis.
Finely divided cobalt particles can be prepared by reduction of cobalt(II) chloride by lithium naphthalenide in glyme.
DescriptionCobalt was discovered by George Brandt in 1737. Cobalt existsin valence states from 0 to 5, with the most stable (+2 and +3)being the most common. Although there is only one stableisotope of cobalt, there are a number of unstable isotopes. Twoof these, cobalt-60 and cobalt-57, are in use commercially.Cobalt-60 is used for cancer treatment and food irradiation.Cobalt-57 has research applications.
Chemical PropertiesCobalt is a silver-gray to black, hard, brittle, magnetic metal. It is relatively rare; the important mineral sources are the arsenides, sulfides, and oxidized forms. It is generally obtained as a by-product of other metals, particularly copper. The fume and dust of cobalt metal is odorless and black. The appearance and odor of cobalt compounds and their dusts and fumes vary with the compound. Cobalt metal in powdered form is incompatible with fused ammonium nitrate, hydrozinium nitrate, and strong oxidizing agents and should be avoided. It ignites on contact with bromide pentafl uoride. Powdered cobalt ignites spontaneously in air. Exposure to cobalt metal fume and dust can occur through inhalation, ingestion, and eye or skin contact.
Chemical PropertiesThere are two allotropic modifications of cobalt, a close-packed hexagonal form (ε) with space group P63/mmc, stable at temperatures below 417 °C; and a face-centered cubic form (α) with space group Fm3m, stable at higher temperatures—up to the melting point. The metal is silvery gray in color. The only naturally occurring isotope, 59Co, is stable, but the other twelve known isotopes are radioactive, their mass numbers ranging from 54 to 64. Half lives range from 0.2 second for 54Co to 5.3 years for the industrially and medically important 60Co.
Cobalt was identified and described by Georg Brandt in 1735, but had to wait until the last decade of the nineteenth century before the new sources of metal supply from New Caledonia and Canada stimulated its metallurgical usage.
Physical propertiesCobalt is a bluish steel-gray metal that can be polished to a bright shine. It is brittle andis not malleable unless alloyed with other metals. It is magnetic, and when alloyed with aluminum and nickel, it is called alnico metal, which acts as a super-magnet with many uses inindustry. Chemically and physically, cobalt acts much as do its two partners, iron (Fe) andnickel (Ni), located on each side of it in period 4 on the periodic table. In particular, iron,cobalt, and nickelare unique in that they possess natural magnetic properties. Cobalt’s meltingpoint is 1,495°C, its boiling point is 2,927°C, and its density is 8.86 g/cm3.
IsotopesThere are 33 isotopes of cobalt, ranging from Co-48 to Co-75, with half-livesranging from a few nanoseconds to 5.272 years for cobalt-60. Cobalt-59 is the onlystable isotope that constitutes almost all (roughly 100%) of the element’s natural presence on Earth. All the other isotopes are radioactive and are created artificially in nuclearreactors or nuclear explosions.
Origin of NameCobalt was given the name kobolds (or kolalds, or kololos) by Germanminers. It means “goblin” (see “History” for more on this story).
OccurrenceCobalt is the 32nd most abundant element on Earth even though it makes up only 0.003%of the Earth’s crust. It is not found in the free metallic state, despite being widely distributedin igneous rocks as minerals. Its two most common mineral ores are cobaltite (CoAsS) anderythrite [Co3(AsO4)2]. These ores are placed in blast furnaces to produce cobalt arsenide(Co2As), which is then treated with sulfuric acid to remove the arsenic. Finally, the productcobalt tetraoxide (Co3O4) is reduced by heat with carbon (Co3O4 + C → 3Co + 2CO2), resulting in cobalt metal.Cobalt is also found in seawater, meteorites, and other ores such as linnaeite, chloanthite,and smaltite, and traces are found mixed with the ores of silver, copper, nickel, zinc, andmanganese. Cobalt ores are found in Canada and parts of Africa, but most of the cobalt usedin the United States is recovered as a by-product of the mining, smelting, and refining of theores of iron, nickel, lead, copper, and zinc.
CharacteristicsCobalt has the highest Curie point of any metal or alloy of cobalt. The Curie point is thetemperature at which an element will lose its magnetism before it reaches its melting point.Cobalt’s Curie point is 1,121°C, and its melting point is 1,495°C. About 25% of all cobaltmined in the world is used as an alloy with other metals. The most important is the alloyalnico, which consists of nickel, aluminum, and cobalt. Alnico is used to make powerful permanent magnets with many uses, such as CT, PET, and MRI medical instruments. It is alsoused for electroplating metals to give a fine surface that resists oxidation.
HistoryCobalt occurs in the mineral cobaltite,smaltite, and erythrite, and is often associated with nickel,silver, lead, copper, and iron ores, from which it is most frequentlyobtained as a by-product. It is also present in meteorites.Important ore deposits are found in Congo-Kinshasa,Australia, Zambia, Russia, Canada, and elsewhere. The U.S.Geological Survey has announced that the bottom of the northcentral Pacific Ocean may have cobalt-rich deposits at relativelyshallow depths in waters close to the Hawaiian Islandsand other U.S. Pacific territories. Cobalt is a brittle, hard metal,closely resembling iron and nickel in appearance. It has a magneticpermeability of about two thirds that of iron. Cobalt tendsto exist as a mixture of two allotropes over a wide temperaturerange; the β-form predominates below 400°C, and the α abovethat temperature. The transformation is sluggish and accountsin part for the wide variation in reported data on physicalproperties of cobalt. It is alloyed with iron, nickel and othermetals to make Alnico, an alloy of unusual magnetic strengthwith many important uses. Stellite alloys, containing cobalt,chromium, and tungsten, are used for high-speed, heavy-duty,high-temperature cutting tools, and for dies. Cobalt is also usedin other magnet steels and stainless steels, and in alloys used injet turbines and gas turbine generators. The metal is used inelectroplating because of its appearance, hardness, and resistanceto oxidation. The salts have been used for centuries forthe production of brilliant and permanent blue colors in porcelain,glass, pottery, tiles, and enamels. It is the principal ingredientin Sevre’s and Thenard’s blue. A solution of the chloride(CoCl2 · 6H2O) is used as sympathetic ink. The cobalt amminesare of interest; the oxide and the nitrate are important. Cobaltcarefully used in the form of the chloride, sulfate, acetate, ornitrate has been found effective in correcting a certain mineraldeficiency disease in animals. Soils should contain 0.13 to 0.30ppm of cobalt for proper animal nutrition. Cobalt is found inVitamin B-12, which is essential for human nutrition. Cobaltof 99.9+% purity is priced at about $250/kg. Cobalt-60, an artificialisotope, is an important gamma ray source, and is extensivelyused as a tracer and a radiotherapeutic agent. Singlecompact sources of Cobalt-60 vary from about $1 to $10/curie,depending on quantity and specific activity. Thirty isotopesand isomers of cobalt are known.
UsesFor alloys; manufacture of cobalt salts; in nuclear technology. Since 60Co can be encapsulated compactly, it has replaced radium in experimental medicine and cancer research. Cobalt is also used in the cobalt bomb, a hydrogen bomb surrounded by a cobalt metal shell. When the nuclear explosion occurs 60Co is formed from 59Co by neutron capture. Considered a "dirty bomb" because of long half-life and intense b- and g radiation. Max permissible concentration of 60Co in air: 10-7mCi/cc, Natl. Bur. Stand. Handb. 69, 31 (1959).
UsesCobalt has many practical uses.Historically, as well as today, different compounds of cobalt have been used for their colorsknown as cobalt blue, cerulean, new blue, smalt, cobalt yellow, and green.For many centuries cobalt was used to color glass, pottery, and porcelain and as an enamel.It is also used as a dye and paint pigment.As mentioned, cobalt alloyed with iron and nickel is used to make powerful permanentmagnets that are used in many industries.A major use is as an alloy with chromium to produce high-speed machine-cutting toolsthat are resistant to high temperatures.A cobalt alloy of copper and tungsten, called “stellite,” also maintains its hardness at hightemperatures, making it an ideal alloy for high-speed drills and cutting tools.The radioisotope cobalt-60, with a half-life of 5.27 years (1925.3 days) through beta (β)emission, decays to form the stable element nickel-60. It is used to test welds and metal castsfor flaws, to irradiate food crops to prolong freshness, as a portable source of ionizing gamma(γ) radiation, for radiation research, and for a medical source of radiation to treat cancers andother diseases.Cobalt is an important trace element for proper human nutrition. It is also a natural component of vitamin B12.
UsesCobalt is used in steel alloys, cementedcarbide abrasives and jet engines.
Production MethodsWorld sources of the metal and the oxide are chiefly fromZaire, Belgium–Luxembourg, Norway, and Finland, in thatorder, with Zaire furnishing 58% of the world’s supply.
Practically all cobalt produced is a by- or coproduct ofother metals, chiefly copper; accordingly, a description of themining process is omitted. The processes used in extractingcobalt from its ores vary according to the type of ore andlocations of the ore deposit.
Arsenical ores are concentrated by hand sorting, gravityseparation, or froth flotation, and are smelted in a blastfurnace with coke and limestone to a speiss (an impuremixture of iron, cobalt, and nickel arsenides). The speiss isground, roasted with salt, and leached with water. Insolublechlorides remaining after the leaching process areground with sulfuric acid, washed, and filtered, and thewashings are added to the liquid from the leaching step.The combined solution is oxidized and then neutralizedwith lime.
Basic ferric arsenate precipitates and is removed, leavinga solution-containing cobalt and nickel. The addition ofsuccessive portions of sodium hydroxide and sodium hypochloriteprecipitates cobalt as the hydroxide, which isinitially pure but finally admixes with nickel hydroxide.The cobalt precipitate is dried, ground, and formed intopellets, which are reduced by heating with charcoal tocobalt metal.
DefinitionChEBI: A cobalt group element atom that has atomic number 27.
DefinitionA lustrous silverybluehard ferromagnetic transition metaloccurring in association with nickel. It isused in alloys for magnets, cutting tools,and electrical heating elements and in catalystsand some paints.
Definitioncobalt: Symbol Co. A light-greytransition element; a.n. 27; r.a.m.58.933; r.d. 8.9; m.p. 1495°C; b.p.2870°C. Cobalt is ferromagneticbelow its Curie point of 1150°C.Small amounts of metallic cobalt arepresent in meteorites but it is usuallyextracted from ore deposits workedin Canada, Morocco, and Za?re. It ispresent in the minerals cobaltite,smaltite, and erythrite but also associatedwith copper and nickel as sulphidesand arsenides. Cobalt ores areusually roasted to the oxide and thenreduced with carbon or water gas.Cobalt is usually alloyed for use. Alnicois a well-known magnetic alloyand cobalt is also used to make stainlesssteels and in high-strength alloysthat are resistant to oxidation at hightemperatures (for turbine blades andcutting tools).
The metal is oxidized by hot airand also reacts with carbon, phosphorus,sulphur, and dilute mineralacids. Cobalt salts, usual oxidationstates II and III, are used to give abrilliant blue colour in glass, tiles,and pottery. Anhydrous cobalt(II)chloride paper is used as a qualitativetest for water and as a heat-sensitiveink. Small amounts of cobalt salts areessential in a balanced diet for mam-mals. Artificiallyproduced cobalt–60 is an importantradioactive tracer andcancer-treatment agent. The elementwas discovered by Georg Brandt(1694–1768) in 1737.
ReactionsCobalt absorbs very little hydrogen even at high temperatures and nitrogen is practicallyinsoluble up to 1200°C. Finely divided cobalt is pyrophoric in air, but the massive metalis scarcely attacked below 300°C. The oxide scale on cobalt heated in air or oxygen up to900° consists of an outside layer of CO3O4 and a layer of CoO next to the metal ; above900°, Co3O4 decomposes and the scale consists of CoO only. Cobalt reacts with manynon-metals when heated, e.g. the halogens, boron, sulphur, phosphorus, arsenic andantimony, the reactions often proceeding with incandescence. Fluorine forms CoF3, whilethe other halogens give the cobalt(II) halide.
Brand nameC.i. 77320;Cobalt-59;Impromin;Inter-con;Kometileneamin;Levacide-c;Orkomin;Panacur;Sofracaps;Tasvite;Trelenium.
World Health Organization (WHO)WHO Comment(non-radioactive forms): The World Health Organization has no information further to theabove regarding preparations containing cobalt or to indicate that they are stillcommercially manufactured.
Air & Water ReactionsBurns brilliantly when exposed to air [Mellor 14:453(1946-1947)]. Insoluble in water.
Reactivity ProfilePyrophoric Cobalt is a reducing agent. Decomposes acetylene in the cold as the metal becomes incandescent [Mellor 14:513(1946-1947]. Incompatible with oxidizing agents such as ammonium nitrate, bromine pentafluoride, and nitryl fluoride.
HazardCobalt is found in most natural foods. Although a necessary trace element, it is toxic to humans if ingested in large amounts. The human body does excrete in urine excessive amounts of cobalt compounds such as found in vitamin B12.
Cobaltous chromate (CoCrO4) is brownish-yellow to grayish-black (the color depends on its purity) is a dangerous carcinogen (causes cancer).
Some years ago, a cobalt additive was used by some beer makers to maintain a foam head on their beer. Those who imbibed excessively developed what is known as beer drinkers syndrome, which caused some deaths from enlarged and flabby hearts.
Health HazardCobalt is an essential element. Its deficiencycan result in pernicious anemia. It is present invitamin B12. Excessive intake of this elementmay result in polycythemia or overproductionof erythrocytes and heart lesions. Exposure toits dusts can produce cough and respiratoryirritation. Chronic inhalation of its dusts orfumes can decrease pulmonary functions andmay cause diffuse nodular fibrosis and otherpulmonary diseases. Skin contact may inducedermal hypersensitivity reactions, producingan allergy-type dermatitis.
Co(II) ion is reported to be genotoxicin vitro and in vivo and carcinogenic inrodents (De Boeck et al. 2003) Occupationalexposure to hard metal (cemented carbide)dust is linked to an increased risk of lungcancer.
Fire HazardLiterature sources indicate that the dust of Cobalt is flammable.
Flammability and ExplosibilityNot classified
reaction suitabilityreagent type: catalyst
core: cobalt
Agricultural UsesCobalt (Co), a metallic element with an atomic weight of 58.94, is one of the transition elements belonging to the Group 9 (formerly Group VIII ) of the Periodic Table. However, in extremely low concentrations ranging from 0.1 to 10parts per billion (ppb), cobalt have been observed to improve growth, transpiration and photosynthesis of cotton, mustard and beans. Cobalt is required by symbiotic micro-organisms (e.g., rhizobia) for the fixation of elemental nitrogen through the formation of vitaminB12.
Cobalt forms a complex with nitrogen atoms of the porphyrin ring structure and provides a prosthetic group for association with nucleotides in vitamin B12 co-enzyme. This complex is called cobamide. Other cobalt functions include leghemoglobin metabolism and ribonucleotide reductase in Rhizobium, and activation of enolase, lecithinase and succinic kinase.
The concentration of cobalt in dry matter of plants ranges from 0.02 to 0.5 ppm. One ppb of cobalt in nutrient solution was found adequate for nitrogen fixation in alfalfa. The water content and catalase activity in leaves increased and the concentration of the cell sap decreased with cobalt application.
Cobalt content in soil is low and variable. In India, for instance, it ranges from 4 to 80ppm. The humus content of the soil influences the availability of cobalt in it. The nature of clay affects the absorption of cobalt from solutions, in the order muscovite > hematite > bentonite = kaolin. An increase in the pH of the soil decreases the availability of cobalt. Cobalt deficiency is more pronounced in coarse sandy soils and under high rainfall conditions. To overcome deficiency, cobalt fertilization with 100to 200g/ha as cobaltous sulphate (CoSO,) is recommended.
Industrial usesCobalt (symbol Co) is a lustrous, silvery-bluemetallic chemical element, resembling nickelbut with a bluish tinge instead of the yellow ofnickel. It is rarer and costlier than nickel andits price has varied widely in recent years.Although allied to nickel, it has distinctive differences.It is more active chemically thannickel. It is dissolved by dilute H2SO4, HNO3,or HCl acids, and is attacked slowly by alkalis.The oxidation rate of pure cobalt is 25 timesthat of nickel. Its power of whitening copperalloys is inferior to that of nickel, but smallamounts in Ni–Cu alloys will neutralize theyellowish tinge of the nickel and make themwhiter. The metal is diamagnetic like nickel, buthas three times the maximum permeability.Like tungsten, it imparts red-hardness to toolsteels. It also hardens alloys to a greater extentthan nickel, especially in the presence of carbon,and can form more chemical compoundsin alloys than nickel.
Its chemical properties resemble, in part,those of both nickel and iron. Cobalt is themetal with the highest Curie temperature(1121°C) and the lowest allotropic transformationtemperature (399°C). Below 421°C, cobaltis close-packed hexagonal; above, it is facecenteredcubic.
Biological ActivityCobalt is a vital trace element in animal nutrition. Ruminants grazing upon cobaltdeficient pastures exhibit retarded growth, loss of appetite and anaemia ; rapid recovery from these symptoms occurs upon feeding the animals with a cobalt-supplemented diet. Cobalt salts are not therefore considered to be particularly toxic to animals, but to man they can in sufficiently large doses irritate the gastro-intestinal tract and cause nausea, vomiting and diarrhoea. Small amounts of cobalt, however, are invaluable in the treatment of pernicious anaemia. The discovery in 1926 of the antipernicious anaemia factor in liver led to the discovery in 1948 of vitamin B12, which was very soon after shown to contain cobalt.
Safety ProfileConfirmed carcinogen with experimental neoplastigenic and tumorigenic data. Poison by intravenous, intratracheal, and intraperitoneal routes. Moderately toxic by ingestion. Inhalation of the dust may cause pulmonary damage. The powder may cause dermatitis. Ingestion of soluble salts produces nausea and vomiting by local irritation. Powdered cobalt igmtes spontaneously in air. Flammable when exposed to heat or flame. Explosive reaction with hydrazinium nitrate, ammonium nitrate + heat, and 1,3,4,7-tetramethylisoindole (at 39OOC). Ignites on contact with bromine pentafluoride. Incandescent reaction with acetylene or nitryl fluoride. See also COBALT COMPOUNDS.
Potential ExposurePossible risk of forming tumors, Suspected reprotoxic hazard. Nickel-aluminumcobalt alloys are used for permanent magnets. Alloys with nickel, aluminum, copper, beryllium, chromium, and molybdenum are used in the electrical, automobile, and aircraft industries. Cobalt is added to tool steels to improve their cutting qualities and is used as a binder in the manufacture of tungsten carbide tools. Various cobalt compounds are used as pigments in enamels, glazes, and paints; as catalysts in afterburners; and in the glass, pottery, photographic, electroplating industries. Radioactive cobalt (60Co) is used in the treatment of cancer. Cobalt has been added to beer to promote formation of foam but cobalt acts with alcohol to produce severe cardiac effects at concentrations as low as 1.2-1.5 mg/L of beer. Cobalt is part of the vitamin B12 molecule and as such is an essential nutrient. The requirement of humans for cobalt in the form of vitamin B12 is about 0.13 μg/day.
First aidIf this chemical gets into the eyes, remove anycontact lenses at once and irrigate immediately for at least15 min, occasionally lifting upper and lower lids. Seek medical attention immediately. If this chemical contacts theskin, remove contaminated clothing and wash immediatelywith soap and water. Seek medical attention immediately. Ifthis chemical has been inhaled, remove from exposure,begin rescue breathing (using universal precautions, including resuscitation mask) if breathing has stopped and
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