Chemistry:Antimony(III) sulfate

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Antimony sulfate
Antimony sulfate.svg
Names
IUPAC name
Antimony(III) sulfate
Other names
Antimonous sulfate
Antimony trisulfate
Diantimony trisulfate
Diantimony tris(sulphate)
Identifiers
3D model (JSmol)
ChemSpider
EC Number
  • 231-207-6
UNII
Properties[2]
Sb2(SO4)3
Molar mass 531.7078 g/mol
Density 3.94 g/cm3[1]
Hydrolysis[1]
Structure[1]
monoclinic
P21/c
a = 13.12 Å, b = 4.75 Å, c = 17.55 Å
α = 90°, β = 126.3°, γ = 90°
881 Å3
Hazards
Safety data sheet MSDS
NIOSH (US health exposure limits):
PEL (Permissible)
TWA 0.5 mg/m3 (as Sb)[3]
REL (Recommended)
TWA 0.5 mg/m3 (as Sb)[3]
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

Antimony sulfate, Sb2(SO4)3, is a hygroscopic salt formed by reacting antimony or its compounds with hot sulfuric acid. It is used in doping of semiconductors and in the production of explosives and fireworks.[4]

Structure

Antimony(III) sulfate consists of interconnected SbO6 octahedra, which the corners are bonded to the sulfate ion.[1]

Production

Antimony(III) sulfate was first produced in 1827 by the reaction of antimony(III) oxide and 18 molar sulfuric acid at 200 °C:[1]

Sb2O3 + 3 H2SO4 → Sb2(SO4)3 + 3 H2O

The concentration of the sulfuric acid is important, as a lower concentration will produce basic antimony oxides, while a higher concentration will produce antimony(III) pyrosulfate. The reaction of elemental antimony and 18 M sulfuric acid will also produce antimony(III) sulfate:[4]

2 Sb + 6 H2SO4 → Sb2(SO4)3 + 3 SO2 + 6 H2O

Chemical properties

Antimony sulfate is deliquescent, hydrolyzing in moist air and water, producing various basic antimony oxides and antimony(III) oxide. It is soluble in acids.[1][4][5]

Uses

Owing to its solubility, antimony sulfate has uses in the doping of semiconductors.[6] It is also used for coating anodes in electrolysis and in the production of explosives and fireworks.[4]

Safety

Antimony(III) sulfate causes irritation to the skin and mucous membranes.[7]

Natural occurrence

Natural analogue of the exact compound is yet unknown. However, basic hydrated Sb sulfates are known as the minerals klebelsbergite[8][9] and coquandite.[10][9]

References

  1. 1.0 1.1 1.2 1.3 1.4 1.5 R. Mercier; J. Douglade; J. Bernard (1976). "Structure cristalline de Sb2O3.3SO3" (in fr). Acta Crystallographica Section B 32 (10): 2787-2791. doi:10.1107/S0567740876008881. 
  2. Lide, D. R., ed (2005). CRC Handbook of Chemistry and Physics (86th ed.). Boca Raton (FL): CRC Press. p. 4.64. ISBN 0-8493-0486-5. 
  3. 3.0 3.1 NIOSH Pocket Guide to Chemical Hazards. "#0036". National Institute for Occupational Safety and Health (NIOSH). https://www.cdc.gov/niosh/npg/npgd0036.html. 
  4. 4.0 4.1 4.2 4.3 Herbst, Karl Albert et al. (1985) Antimony and antimony compounds in Ullmann's Encyclopedia of Industrial Chemistry 5th ed., vol. A3, p. 70. ISBN:3-527-20103-3.
  5. Nicholas C. Norman (31 December 1997). Chemistry of arsenic, antimony, and bismuth. Springer. pp. 193–. ISBN 978-0-7514-0389-3. https://books.google.com/books?id=vVhpurkfeN4C&pg=PA193. 
  6. Method of forming phase change layer, method of manufacturing a storage node using the same, and method of manufacturing phase change memory device using the same – Samsung Electronics Co., Ltd. Freepatentsonline.com (2007-01-02). Retrieved on 2011-12-23.
  7. Antimony(III) Sulfate Material Safety Data Sheet . Prochemonline.
  8. "Klebelsbergite". https://www.mindat.org/min-2223.html. 
  9. 9.0 9.1 "List of Minerals". 21 March 2011. https://www.ima-mineralogy.org/Minlist.htm. 
  10. "Coquandite". https://www.mindat.org/min-1125.html.