Cobalt(II) carbonate

Cobalt(II) carbonate
Co2+ CO32−
Cobalt(II) carbonate powder
Cobalt(II) carbonate powder
Names
IUPAC name
Cobalt(II) carbonate
Other names
Cobaltous carbonate; cobalt(II) salt
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.007.428
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/CH2O3.Co/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2 ☒N
    Key: ZOTKGJBKKKVBJZ-UHFFFAOYSA-L ☒N
  • InChI=1/CH2O3.Co/c2-1(3)4;/h(H2,2,3,4);/q;+2/p-2
    Key: ZOTKGJBKKKVBJZ-NUQVWONBAB
SMILES
  • C(=O)([O-])[O-].[Co+2]
Properties
Chemical formula
CoCO3
Molar mass 118.941 g/mol
Appearance pink solid
Density 4.13 g/cm3
Melting point 427 °C (801 °F; 700 K) [3]
decomposes before melting to cobalt(II) oxide (anhydrous)
140 °C (284 °F; 413 K)
decomposes (hexahydrate)
Solubility in water
0.000142 g/100 mL (20 °C)[1]
Solubility product (Ksp)
1.0·10−10[2]
Solubility soluble in acid
negligible in alcohol, methyl acetate
insoluble in ethanol
Refractive index (nD)
1.855
Structure
Crystal structure
Rhombohedral (anhydrous)
Trigonal (hexahydrate)
Thermochemistry
Std molar
entropy (S298)
79.9 J/mol·K[3]
Std enthalpy of
formation fH298)
−722.6 kJ/mol[3]
Gibbs free energy fG)
−651 kJ/mol[3]
Hazards
GHS labelling:
Pictograms
GHS07: Exclamation markGHS08: Health hazard[4]
Signal word
Warning
Hazard statements
H302, H315, H317, H319, H335, H351[4]
Precautionary statements
P261, P280, P305+P351+P338[4]
NFPA 704 (fire diamond)
NFPA 704 four-colored diamond
2
0
0
Lethal dose or concentration (LD, LC):
LD50 (median dose)
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).
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Infobox references

Cobalt(II) carbonate is the inorganic compound with the formula CoCO3. This pink 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]

Preparation and structure

Structure of solid cobalt(II) carbonate shown with space-filling ions. Color code: red = O, green = Co, blck = C

It is prepared by combining solutions of cobalt(II) 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

Aqueous solutions of cobalt chloride can be prepared from cobalt(II) carbonate with hydrochloric acid according to this idealized equation:[8]

CoCO3 + 2 HCl + 3 H2O → CoCl2·(H2O)4 + CO2

The reaction of cobalt(II) carbonate and acetylacetone in the presence of hydrogen peroxide gives tris(acetylacetonato)cobalt(III).[9]

Heating the carbonate in air (calcining) is accompanied by partial oxidation:

6 CoCO3 + O2 → 2 Co3O4 + 6 CO2

The resulting Co3O4 converts reversibly to CoO at high temperatures.[10]

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.[11]

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]

Sodium tris(carbonato)cobalt(III) is a cobalt(III) complex containing three carbonate ligands.

Safety

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

References

  1. ^ 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.
  2. ^ "Solubility product constants". Archived from the original on 2012-06-15. Retrieved 2012-05-17.
  3. ^ a b c d "Cobalt(II) carbonate".
  4. ^ a b c Sigma-Aldrich Co., Cobalt(II) carbonate. Retrieved on 2014-05-06.
  5. ^ a b c 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 3527306730.
  6. ^ a b "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. ^ O. Glemser (1963). "Cobalt(II) Chloride". In G. Brauer (ed.). Handbook of Preparative Inorganic Chemistry, 2nd Ed. Vol. 2. NY, NY: Academic Press. p. 1515.
  9. ^ Bryant, Burl E.; Fernelius, W. Conard (1957). "Cobalt(III) Acetylacetonate". Inorganic Syntheses. pp. 188–189. doi:10.1002/9780470132364.ch53. ISBN 9780470132364. {{cite book}}: ISBN / Date incompatibility (help)
  10. ^ El-Shobaky, G. A.; Ahmad, A. S.; Al-Noaim, A. N.; El-Shobaky, H. G. (1996). "Thermal Decomposition of Basic Cobalt and Copper Carbonates". Journal of Thermal Analysis and Calorimetry. 46: 1801. doi:10.1007/BF01980784.
  11. ^ 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.
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