Copper(II) oxide
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| Names | |
|---|---|
| IUPAC name Copper(II) oxide | |
| Other names Cupric oxide | |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.013.882 |
| EC Number |
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PubChem CID | |
| RTECS number |
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| UNII | |
CompTox Dashboard (EPA) | |
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| Properties | |
| CuO | |
| Molar mass | 79.545 g/mol |
| Appearance | black to brown powder |
| Density | 6.315 g/cm3 |
| Melting point | 1,326 °C (2,419 °F; 1,599 K) |
| Boiling point | 2,000 °C (3,630 °F; 2,270 K) |
| insoluble | |
| Solubility | soluble in ammonium chloride, potassium cyanide insoluble in alcohol, ammonium carbonate |
| Band gap | 1.2 eV |
| +238.9·10−6 cm3/mol | |
Refractive index (nD) | 2.63 |
| Structure | |
| monoclinic, mS8[1] | |
| C2/c, #15 | |
a = 4.6837, b = 3.4226, c = 5.1288 α = 90°, β = 99.54°, γ = 90° | |
| Thermochemistry | |
Std molar entropy (S⦵298) | 43 J·mol−1·K−1 |
Std enthalpy of formation (ΔfH⦵298) | −156 kJ·mol−1 |
| Hazards | |
| GHS labelling: | |
 | |
| Warning | |
| H410 | |
| P273, P391, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | Non-flammable |
| NIOSH (US health exposure limits): | |
PEL (Permissible) | TWA 1 mg/m3 (as Cu)[2] |
REL (Recommended) | TWA 1 mg/m3 (as Cu)[2] |
IDLH (Immediate danger) | TWA 100 mg/m3 (as Cu)[2] |
| Safety data sheet (SDS) | Fisher Scientific |
| Related compounds | |
Other anions | Copper(II) sulfide |
Other cations | Nickel(II) oxide Zinc oxide |
Related compounds | Copper(I) oxide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Copper(II) oxide or cupric oxide is an inorganic compound with the formula CuO. A black solid, it is one of the two stable oxides of copper, the other being Cu2O or copper(I) oxide (cuprous oxide). As a mineral, it is known as tenorite, or sometimes black copper. It is a product of copper mining and the precursor to many other copper-containing products and chemical compounds.[3]
Production
[edit]It is produced on a large scale by pyrometallurgy, as one stage in extracting copper from its ores. The ores are treated with an aqueous mixture of ammonium carbonate, ammonia, and oxygen to ultimately give copper(II) ammine complex carbonates, such as [Cu(NH3)4]CO3. After extraction from the residues and after separation from iron, lead, etc. impurities, the carbonate salt is decomposed with steam to give CuO.[3]
It can be formed by heating copper in air at around 300–800 °C:
- 2 Cu + O2 → 2 CuO
For laboratory uses, copper(II) oxide is conveniently prepared by pyrolysis of copper(II) nitrate or basic copper(II) carbonate:[4]
- 2 Cu(NO3)2 → 2 CuO + 4 NO2 + O2 (180°C)
- Cu2(OH)2CO3 → 2 CuO + CO2 + H2O
Dehydration of cupric hydroxide has also been demonstrated:
- Cu(OH)2 → CuO + H2O
Reactions
[edit]Copper(II) oxide reacts with mineral acids such as hydrochloric acid, sulfuric acid, and nitric acid to give the corresponding hydrated copper(II) salts:[4]
- CuO + 2 HNO3 → Cu(NO3)2 + H2O
- CuO + 2 HCl → CuCl2 + H2O
- CuO + H2SO4 → CuSO4 + H2O
In presence of water it reacts with concentrated alkali to form the corresponding cuprate salts:
- 2 NaOH + CuO + H2O → Na2[Cu(OH)4]
It can also be reduced to copper metal using hydrogen, carbon monoxide, and carbon:
- CuO + H2 → Cu + H2O
- CuO + CO → Cu + CO2
- 2 CuO + C → 2Cu + CO2
When cupric oxide is substituted for iron oxide in thermite the resulting mixture is a low explosive, not an incendiary.
Structure and physical properties
[edit]Copper(II) oxide belongs to the monoclinic crystal system. The copper atom is coordinated by 4 oxygen atoms in an approximately square planar configuration.[1]
The work function of bulk CuO is 5.3 eV.[5]
Uses
[edit]As a significant product of copper mining, copper(II) oxide is the starting point for the production of many other copper salts. For example, many wood preservatives are produced from copper oxide.[3]
Cupric oxide is used as a pigment in ceramics to produce blue, red, and green, and sometimes gray, pink, or black glazes.[3]
It is incorrectly used as a dietary supplement in animal feed.[6] Due to low bioactivity, negligible copper is absorbed.[7]
It is used when welding with copper alloys.[8]
A copper oxide electrode formed part of the early battery type known as the Edison–Lalande cell. Copper oxide was also used in a lithium battery type (IEC 60086 code "G").
Pyrotechnics and fireworks
[edit]Used as moderate blue coloring agent in blue flame compositions with additional chlorine donors and oxidizers such as chlorates and perchlorates. Providing oxygen it can be used as flash powder oxidizer with metal fuels such as magnesium, aluminium, or magnalium powder. Sometimes it is used in strobe effects and thermite compositions as crackling stars effect.
Similar compounds
[edit]An example of natural copper(I,II) oxide is the mineral paramelaconite, Cu+2Cu2+2O3.[9][10]
See also
[edit]References
[edit]- ^ a b The effect of hydrostatic pressure on the ambient temperature structure of CuO, Forsyth J.B., Hull S., J. Phys.: Condens. Matter 3 (1991) 5257–5261, doi:10.1088/0953-8984/3/28/001. Crystallographic point group: 2/m or C2h. Space group: C2/c. Lattice parameters: a = 4.6837(5), b = 3.4226(5), c = 5.1288(6), α = 90°, β = 99.54(1)°, γ = 90°.
- ^ a b c NIOSH Pocket Guide to Chemical Hazards. "#0150". National Institute for Occupational Safety and Health (NIOSH).
- ^ a b c d Richardson, H. Wayne (2002). "Copper Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a07_567. ISBN 978-3527306732.
- ^ a b O. Glemser and H. Sauer (1963). "Copper, Silver, Gold". In G. Brauer (ed.). Handbook of Preparative Inorganic Chemistry, 2nd Ed. Vol. 1. NY, NY: Academic Press.
- ^ F. P. Koffyberg and F. A. Benko (1982). "A photoelectrochemical determination of the position of the conduction and valence band edges of p-type CuO". J. Appl. Phys. 53 (2): 1173. Bibcode:1982JAP....53.1173K. doi:10.1063/1.330567.
- ^ "Uses of Copper Compounds: Other Copper Compounds". Copper Development Association. 2007. Archived from the original on 2013-08-15. Retrieved 2007-01-27.
- ^ Baker, David H. (1999). "Cupric Oxide Should Not be Used as a Copper Supplement for Either Animals or Humans". The Journal of Nutrition. 129 (12): 2278–2279. doi:10.1093/jn/129.12.2278. PMID 10573563.
- ^ "Cupric Oxide Data Sheet". Hummel Croton Inc. 2006-04-21. Archived from the original on 2011-07-07. Retrieved 2007-02-01.
- ^ "Paramelaconite".
- ^ "List of Minerals". 21 March 2011.
External links
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