Jump to content

Peroxydisulfuric acid

From Wikipedia, the free encyclopedia
(Redirected from Peroxodisulfuric acid)
Peroxydisulfuric acid
Names
IUPAC names
μ-peroxido-bis(hydroxidodioxidosulfur)
peroxydisulfuric acid
Other names
Persulfuric acid, Peroxodisulfuric acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/H2O8S2/c1-9(2,3)7-8-10(4,5)6/h(H,1,2,3)(H,4,5,6) checkY
    Key: JRKICGRDRMAZLK-UHFFFAOYSA-N checkY
  • InChI=1/H2O8S2/c1-9(2,3)7-8-10(4,5)6/h(H,1,2,3)(H,4,5,6)/f/h1,4H
  • InChI=1/H2O8S2/c1-9(2,3)7-8-10(4,5)6/h(H,1,2,3)(H,4,5,6)
    Key: JRKICGRDRMAZLK-UHFFFAOYAS
  • O=S(=O)(OOS(=O)(=O)O)O
Properties
H2O8S2
Molar mass 194.13 g·mol−1
Appearance Colourless solid
Melting point 65 °C (149 °F; 338 K) (decomposes)
soluble
Conjugate base Peroxydisulfate
Related compounds
Other cations
Potassium persulfate
Sodium persulfate
Ammonium persulfate
Related compounds
Peroxymonosulfuric acid
Pyrosulfuric acid
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
☒N verify (what is checkY☒N ?)

Peroxydisulfuric acid is an inorganic compound with a chemical formula (HO3SO)2. Also called Marshall's acid after Professor Hugh Marshall, who discovered it in 1891.[1]

Structure and bonding

[edit]

This oxoacid features sulfur in its +6 oxidation state and a peroxide group. Sulfur adopts the usual tetrahedral geometry.[2]

Synthesis

[edit]

The acid is prepared by the reaction of chlorosulfuric acid with hydrogen peroxide:[3]

2 ClSO3H + H2O2 → H2S2O8 + 2 HCl

Another method is the electrolysis of moderately concentrated sulfuric acid (60-70%) with platinum electrodes at high current density and voltage:

H2SO4 + H2O → H3O+ + HSO4 (dissociation of sulfuric acid)
2 HSO4 → H2S2O8 + 2 e (E0 = +2.4V) (bisulfate oxidation)
2 H2SO4 → H2S2O8 + H2 (overall reaction)
3 H2O → O3 + 6 H+ (ozone produced as a side product)

Uses

[edit]

Peroxydisulfuric acid is a precursor to several salts including sodium peroxydisulfate, potassium peroxydisulfate, and ammonium peroxydisulfate. These salts are used to initiate the polymerization of acrylonitrile, styrene, and related monomers. This application exploits the tendency of the peroxydisulfate anion to undergo homolysis to produce radicals. They are also used as cleaning of circuit boards.[3]

See also

[edit]

References

[edit]
  1. ^ Senning, Alexander (2006-10-30). Elsevier's Dictionary of Chemoetymology: The Whys and Whences of Chemical Nomenclature and Terminology. ISBN 9780080488813.
  2. ^ Greenwood, Norman N.; Earnshaw, Alan (1997). Chemistry of the Elements (2nd ed.). Butterworth-Heinemann. ISBN 978-0-08-037941-8.
  3. ^ a b Harald Jakob, Stefan Leininger, Thomas Lehmann, Sylvia Jacobi, Sven Gutewort. "Peroxo Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a19_177.pub2. ISBN 978-3527306732.{{cite encyclopedia}}: CS1 maint: multiple names: authors list (link)