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Copper(I) sulfide

From Wikipedia, the free encyclopedia
Copper(I) sulfide
Names
IUPAC name
Copper(I) sulfide
Other names
Cuprous sulfide
Chalcocite
Copper glance
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard100.040.751Edit this at Wikidata
RTECS number
  • GL8910000
UNII
  • InChI=1S/2Cu.S/q2*+1;-2 checkY
    Key: AQMRBJNRFUQADD-UHFFFAOYSA-N checkY
  • InChI=1/2Cu.S/q2*+1;-2
    Key: AQMRBJNRFUQADD-UHFFFAOYAN
  • [Cu+].[Cu+].[S-2]
Properties
Cu2S
Molar mass159.16 g/mol
Density5.6 g/cm3[1][page needed]
Melting point1,130 °C (2,070 °F; 1,400 K)[2]
insoluble[citation needed]
Solubility inhydrochloric acidslightly soluble[citation needed][quantify]
Solubility inammonium hydroxidesoluble[citation needed][quantify]
Hazards[4]
NFPA 704 (fire diamond)
Flash pointNonflammable
NIOSH (US health exposure limits):[5]
PEL (Permissible)
TWA1 mg/m3 (as Cu)
REL (Recommended)
TWA1 mg/m3 (as Cu)
IDLH (Immediate danger)
TWA100 mg/m3 (as Cu)
Safety data sheet (SDS)Sigma-Aldrich[3]
Related compounds
Otheranions
Othercations
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa).
checkY verify (what is checkY☒N ?)
Chemical compound

Copper(I) sulfide is acopper sulfide, a chemical compound ofcopper andsulfur. It has thechemical formula ofCu2S. It is found in nature as the mineralchalcocite. It has a narrow range of stoichiometry ranging fromCu1.997S toCu2.000S.[6] Samples are typically black.[citation needed]

Preparation and reactions

[edit]

Cu2S can be prepared by treating copper with sulfur orH2S.[2] The rate depends on the particle size and temperature.[7]Cu2S reacts with oxygen to formSO2:[8][page needed]

2 Cu2S + 3 O2 → 2 Cu2O + 2 SO2

The production of copper from chalcocite is a typical process in extracting the metal from ores. Usually, the conversion involves roasting, to giveCu2O as an intermediate which is further reduced to the metal, and sulfur dioxide:[8][page needed]

Cu2S + O2 → 2 Cu + SO2

Copper(I) oxide readily converts tocopper(II) oxide when heated in the presence of oxygen, and to copper metal upon heating in a reducing environment. (cf.Carbothermic reduction)

Structure

[edit]
Crystals of chalcocite (mineral form of Cu2S).

Stoichiometric

[edit]

Two forms (a dimorphism) ofCu2S are known. The so-called low temperaturemonoclinic form ("low-chalcocite") has a complex structure with 96 copper atoms in the unit cell.[9] The hexagonal form, stable above 104 °C (219 °F),[10][page needed] has 24 crystallographically distinct Cu atoms. Its structure has been described as approximating to ahexagonal close packed array of sulfur atoms with Cu atoms in planar 3 coordination. This structure was initially assigned an orthorhombic cell due to the twinning of the sample crystal.

Non-stoichiometric

[edit]

As illustrated by the mineraldjurleite, a cuprous sulfide is also known.[clarification needed] With the approximate formulaCu1.96S, this material isnon-stoichiometric (rangeCu1.934S-Cu1.965S and has a monoclinic structure with 248 copper and 128 sulfur atoms in the unit cell.[9]Cu2S andCu1.96S are similar in appearance and hard to distinguish one from another.[11]

Phase transition

[edit]

Theelectrical resistivity increases abruptly at the phase transition point around 104 °C (219 °F), with the precise temperature depending on the stoichiometry.[12][13]

See also

[edit]

References

[edit]
  1. ^Patnaik, Pradyot (2003).Handbook of inorganic chemicals. New York: McGraw-Hill.ISBN 0-07-049439-8.
  2. ^abGreenwood, Norman N.; Earnshaw, Alan (1984).Chemistry of the Elements. Oxford:Pergamon Press. p. 1373.ISBN 978-0-08-022057-4.
  3. ^"Copper (I) sulfite, SDS".Sigma-Aldrich. Retrieved18 July 2025.
  4. ^Sigma-Aldrich Co.,Copper(I) sulfide. Retrieved on 18-07-2025.
  5. ^"NIOSH Pocket Guide to Chemical Hazards".
  6. ^Potter, R. W. (1977). "An electrochemical investigation of the system copper-sulfur".Economic Geology.72 (8):1524–1542.Bibcode:1977EcGeo..72.1524P.doi:10.2113/gsecongeo.72.8.1524.
  7. ^Blachnik R., Müller A. (2000). "The formation of Cu2S from the elements I. Copper used in form of powders".Thermochimica Acta.361: 31.doi:10.1016/S0040-6031(00)00545-1.
  8. ^abWiberg, Egon; Wiberg, Nils; Holleman, A. F. (2001).Inorganic chemistry (1st English ed.). San Diego : Berlin ; New York: Academic Press ; De Gruyter.ISBN 0-12-352651-5.
  9. ^abEvans, H. T. (1979). "Djurleite (Cu1.94S) and Low Chalcocite (Cu2S): New Crystal Structure Studies".Science.203 (4378):356–8.Bibcode:1979Sci...203..356E.doi:10.1126/science.203.4378.356.PMID 17772445.S2CID 6132717.
  10. ^Wells, A. F. (1984).Structural inorganic chemistry (5th ed.). Oxford [Oxfordshire] : New York: Clarendon Press ; Oxford University Press.ISBN 0-19-855370-6.
  11. ^Evans H.T. (1981)."Copper coordination in low chalcocite and djurleite and other copper-rich sulfides"(PDF).American Mineralogist.66 (7–8):807–818.
  12. ^Garisto, Dan (2023-08-16)."LK-99 isn't a superconductor — how science sleuths solved the mystery".Nature.620 (7975):705–706.Bibcode:2023Natur.620..705G.doi:10.1038/d41586-023-02585-7.PMID 37587284.S2CID 260955242.
  13. ^Jain, Prashant K. "Phase transition of copper (I) sulfide and its implication for purported superconductivity of LK-99."arXiv preprint arXiv:2308.05222 (2023).
Cu(0,I)
Cu(I)
Cu(I,II)
Cu(II)
Cu(III)
Cu(IV)
Sulfides(S2−)
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