Cobalt(II) carbonate

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Cobalt(II) carbonate
Calcium-carbonate-xtal-3D-SF.png
Cobalt(2) carbonate.jpg
Names
IUPAC name
Cobalt(II) carbonate
Other names
Cobaltous carbonate; cobalt(II) salt
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.428 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • InChI=1S/CH2O3.Co/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2 X mark.svgN
    Key: ZOTKGJBKKKVBJZ-UHFFFAOYSA-L X mark.svgN
  • InChI=1/CH2O3.Co/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2
    Key: ZOTKGJBKKKVBJZ-NUQVWONBAB
  • C(=O)([O-])[O-].[Co+2]
Properties
CoCO3
Molar mass 118.941 g/mol
Appearancered-pink solid
Density 4.13 g/cm3
Melting point 427 °C (801 °F; 700 K) [1]
decomposes before melting to cobalt(II) oxide (anhydrous)
140 °C (284 °F; 413 K)
decomposes (hexahydrate)
0.000142 g/100 mL (20 °C) [2]
1.0·10−10 [3]
Solubility soluble in acid
negligible in alcohol, methyl acetate
insoluble in ethanol
1.855
Structure
Rhombohedral (anhydrous)
Trigonal (hexahydrate)
Thermochemistry
Std molar
entropy
(S298)
79.9 J/mol·K [1]
−722.6 kJ/mol [1]
-651 kJ/mol [1]
Hazards
GHS labelling:
GHS-pictogram-exclam.svg GHS-pictogram-silhouette.svg [4]
Warning
H302, H315, H317, H319, H335, H351 [4]
P261, P280, P305+P351+P338 [4]
NFPA 704 (fire diamond)
NFPA 704.svgHealth 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g. chloroformFlammability 0: Will not burn. E.g. waterInstability 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g. liquid nitrogenSpecial hazards (white): no code
2
0
0
Lethal dose or concentration (LD, LC):
640 mg/kg (oral, rats)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Cobalt(II) carbonate is the inorganic compound with the formula CoCO3. This reddish paramagnetic solid is an intermediate in the hydrometallurgical purification of cobalt from its ores. It is an inorganic pigment, and a precursor to catalysts. [5] Cobalt(II) carbonate also occurs as the rare red/pink mineral spherocobaltite. [6]

Contents

Preparation and structure

It is prepared by combining solutions cobaltous sulfate and sodium bicarbonate:

CoSO4 + 2 NaHCO3 → CoCO3 + Na2SO4 + H2O + CO2

This reaction is used in the precipitation of cobalt from an extract of its roasted ores. [5]

CoCO3 adopts a structure like calcite, consisting of cobalt in an octahedral coordination geometry. [7]

Reactions

Like most transition metal carbonates, cobalt carbonate is insoluble in water, but is readily attacked by mineral acids:

CoCO3 + 2 HCl + 5 H2O → [Co(H2O)6]Cl2 + CO2

It is used to prepare many coordination complexes. The reaction of cobalt(II) carbonate and acetylacetone in the presence of hydrogen peroxide gives tris(acetylacetonato)cobalt(III). [8]

Heating the carbonate proceeds in a typical way for calcining, except that the product becomes partially oxidized:

6 CoCO3 + O2 → 2 Co3O4 + 6 CO2

The resulting Co3O4 converts reversibly to CoO at high temperatures. [9]

Uses

Cobalt carbonate is a precursor to cobalt carbonyl and various cobalt salts. It is a component of dietary supplements since cobalt is an essential element. It is a precursor to blue pottery glazes, famously in the case of Delftware.

At least two cobalt(II) carbonate-hydroxides are known: Co2(CO3)(OH)2 and Co6(CO3)2(OH)8·H2O. [10]

The moderately rare spherocobaltite is a natural form of cobalt carbonate, with good specimens coming especially from the Republic of Congo. "Cobaltocalcite" is a cobaltiferous calcite variety that is quite similar in habit to spherocobaltite. [6]

Safety

Toxicity has rarely been observed. Animals, including humans, require trace amounts of cobalt, a component of vitamin B12. [5]

Related Research Articles

<span class="mw-page-title-main">Magnesium carbonate</span> Chemical compound

Magnesium carbonate, MgCO3, is an inorganic salt that is a colourless or white solid. Several hydrated and basic forms of magnesium carbonate also exist as minerals.

In chemistry, water(s) of crystallization or water(s) of hydration are water molecules that are present inside crystals. Water is often incorporated in the formation of crystals from aqueous solutions. In some contexts, water of crystallization is the total mass of water in a substance at a given temperature and is mostly present in a definite (stoichiometric) ratio. Classically, "water of crystallization" refers to water that is found in the crystalline framework of a metal complex or a salt, which is not directly bonded to the metal cation.

<span class="mw-page-title-main">Nickel(II) chloride</span> Chemical compound

Nickel(II) chloride (or just nickel chloride) is the chemical compound NiCl2. The anhydrous salt is yellow, but the more familiar hydrate NiCl2·6H2O is green. Nickel(II) chloride, in various forms, is the most important source of nickel for chemical synthesis. The nickel chlorides are deliquescent, absorbing moisture from the air to form a solution. Nickel salts have been shown to be carcinogenic to the lungs and nasal passages in cases of long-term inhalation exposure.

<span class="mw-page-title-main">Manganese(II) carbonate</span> Chemical compound

Manganese carbonate is a compound with the chemical formula MnCO3. Manganese carbonate occurs naturally as the mineral rhodochrosite but it is typically produced industrially. It is a pale pink, water-insoluble solid. Approximately 20,000 metric tonnes were produced in 2005.

<span class="mw-page-title-main">Nickel(II) carbonate</span> Chemical compound

Nickel(II) carbonate describes one or a mixture of inorganic compounds containing nickel and carbonate. From the industrial perspective, an important nickel carbonate is basic nickel carbonate with the formula Ni4CO3(OH)6(H2O)4. Simpler carbonates, ones more likely encountered in the laboratory, are NiCO3 and its hexahydrate. All are paramagnetic green solids containing Ni2+ cations. The basic carbonate is an intermediate in the hydrometallurgical purification of nickel from its ores and is used in electroplating of nickel.

<span class="mw-page-title-main">Manganese(II) sulfate</span> Chemical compound

Manganese(II) sulfate usually refers to the inorganic compound with the formula MnSO4·H2O. This pale pink deliquescent solid is a commercially significant manganese(II) salt. Approximately 260,000 tonnes of manganese(II) sulfate were produced worldwide in 2005. It is the precursor to manganese metal and many other chemical compounds. Manganese-deficient soil is remediated with this salt.

<span class="mw-page-title-main">Cobalt(II) sulfate</span> Inorganic compound

Cobalt(II) sulfate is any of the inorganic compounds with the formula CoSO4(H2O)x. Usually cobalt sulfate refers to the hexa- or heptahydrates CoSO4.6H2O or CoSO4.7H2O, respectively. The heptahydrate is a red solid that is soluble in water and methanol. Since cobalt(II) has an odd number of electrons, its salts are paramagnetic.

<span class="mw-page-title-main">Strontium sulfide</span> Chemical compound

Strontium sulfide is the inorganic compound with the formula SrS. It is a white solid. The compound is an intermediate in the conversion of strontium sulfate, the main strontium ore called celestite, to other more useful compounds.

<span class="mw-page-title-main">Manganese(II) acetate</span> Chemical compound

Manganese(II) acetate are chemical compounds with the formula Mn(CH3CO2)2·(H2O)n where n = 0, 2, 4. These materials are white or pale pink solids. Some of these compounds are used as a catalyst and as fertilizer.

<span class="mw-page-title-main">Copper(II) phosphate</span> Chemical compound

Copper(II) phosphate are inorganic compounds with the formula Cu3(PO4)2. They can be regarded as the cupric salts of phosphoric acid. Anhydrous copper(II) phosphate and a trihydrate are blue solids.

Aluminium carbonate (Al2(CO3)3), is a carbonate of aluminium. It is not well characterized; one authority says that simple carbonates of aluminium are not known. However related compounds are known, such as the basic sodium aluminium carbonate mineral dawsonite (NaAlCO3(OH)2) and hydrated basic aluminium carbonate minerals scarbroite (Al5(CO3)(OH)13•5(H2O)) and hydroscarbroite (Al14(CO3)3(OH)36•nH2O).

<span class="mw-page-title-main">Nickel(II) acetate</span> Chemical compound

Nickel(II) acetate is the name for the coordination compounds with the formula Ni(CH3CO2)2·x H2O where x can be 0, 2, and 4. The green tetrahydrate Ni(CH3CO2)2·4 H2O is most common. It is used for electroplating.

<span class="mw-page-title-main">Nickel oxyacid salts</span>

The Nickel oxyacid salts are a class of chemical compounds of nickel with an oxyacid. The compounds include a number of minerals and industrially important nickel compounds.

<span class="mw-page-title-main">Fluorocarbonate</span> Class of chemical compounds

A carbonate fluoride, fluoride carbonate, fluorocarbonate or fluocarbonate is a double salt containing both carbonate and fluoride. The salts are usually insoluble in water, and can have more than one kind of metal cation to make more complex compounds. Rare-earth fluorocarbonates are particularly important as ore minerals for the light rare-earth elements lanthanum, cerium and neodymium. Bastnäsite is the most important source of these elements. Other artificial compounds are under investigation as non-linear optical materials and for transparency in the ultraviolet, with effects over a dozen times greater than Potassium dideuterium phosphate.

The carbonate oxalates are mixed anion compounds that contain both carbonate (CO3) and oxalate (C2O4) anions. Most compounds incorporate large trivalent metal ions, such as the rare earth elements. Some carbonate oxalate compounds of variable composition are formed by heating oxalates.

<span class="mw-page-title-main">Carbonatobis(ethylenediamine)cobalt(III) chloride</span> Chemical compound

Carbonatobis(ethylenediamine)cobalt(III) chloride is a salt with the formula [CoCO3(en)2]Cl (en = ethylenediamine). It is a red diamagnetic solid that is soluble in water. It is the monochloride salt of a cationic carbonate complex [CoCO3(en)2]+. The chloride ion in this salt readily undergoes ion exchange. The compound is synthesized by the oxidation of a mixture of cobalt(II) chloride, lithium hydroxide, and ethylenediamine in the presence of carbon dioxide:

Cobalt compounds are chemical compounds formed by cobalt with other elements.

<span class="mw-page-title-main">Sodium tris(carbonato)cobalt(III)</span> Chemical compound

Sodium tris(carbonato)cobalt(III) is the inorganic compound with the formula Na3Co(CO3)3•3H2O. The salt contains an olive-green metastable cobalt(III) coordination complex. The salt, a homoleptic metal carbonato complex, is sometimes referred to as the “Field-Durrant precursor” and is prepared by the “Field-Durrant synthesis”. It is used in the synthesis of other cobalt(III) complexes. Otherwise cobalt(III) complexes are generated from cobalt(II) precursors, a process that requires an oxidant.

<span class="mw-page-title-main">Transition metal carbonate and bicarbonate complexes</span>

Transition metal carbonate and bicarbonate complexes are coordination compounds containing carbonate (CO32-) and bicarbonate (HCO3-) as ligands. The inventory of complexes is large, enhanced by the fact that the carbonate ligand can bind metal ions in a variety of bonding modes. They illustrate the fate of low valent complexes when exposed to air.

Carbonate nitrates are mixed anion compounds containing both carbonate and nitrate ions.

References

  1. 1 2 3 4 "Cobalt(II) carbonate".
  2. Haynes, W.M., ed. (2017). CRC Handbook of Chemistry and Physics (97th ed.). CRC Press, Taylor & Francis Group. pp. 4–58. ISBN   978-1-4987-5429-3.
  3. "Solubility product constants". Archived from the original on 2012-06-15. Retrieved 2012-05-17.
  4. 1 2 3 Sigma-Aldrich Co., Cobalt(II) carbonate. Retrieved on 2014-05-06.
  5. 1 2 3 Donaldson, John Dallas; Beyersmann, Detmar (2005). "Cobalt and Cobalt Compounds". Ullmann's Encyclopedia of Industrial Chemistry . Weinheim: Wiley-VCH. doi:10.1002/14356007.a07_281.pub2. ISBN   978-3527306732.
  6. 1 2 "Spherocobaltite: Spherocobaltite mineral information and data". www.mindat.org. Retrieved 7 August 2018.
  7. Pertlik, F. (1986). "Structures of hydrothermally synthesized cobalt(II) carbonate and nickel(II) carbonate". Acta Crystallographica Section C. 42: 4–5. doi:10.1107/S0108270186097524.
  8. Bryant, Burl E.; Fernelius, W. Conard (1957). "Cobalt(III) Acetylacetonate". Inorganic Syntheses. pp. 188–189. doi:10.1002/9780470132364.ch53. ISBN   9780470132364.
  9. G.A. El-Shobaky, A.S. Ahmad, A.N. Al-Noaimi and H.G. El-Shobaky Journal of Thermal Analysis and Calorimetry 1996, Volume 46, Number 6 , pp.1801-1808. online abstract
  10. Bhojane, Prateek; Le Bail, Armel; Shirage, Parasharam M. (2019). "A Quarter of a Century After its Synthesis and with >200 Papers Based on its Use, 'Co(CO3)0.5(OH)0.11H2O′ Proves to be Co6(CO3)2(OH)8·H2O from Synchrotron Powder Diffraction Data". Acta Crystallographica Section C: Structural Chemistry. 75 (Pt 1): 61–64. doi:10.1107/S2053229618017734. PMID   30601132. S2CID   58657483.