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Peroxymonosulfuric acid

From Wikipedia, the free encyclopedia

Pe roxym onos ulfuric acid, (H2SO5), also know n as pe rs ulfuric acid, pe roxys ulfuric acid, or Caro's acid,
Peroxymonosulfuric acid
has a melting point of 45 degree Celsius. In this acid, the S(VI) center adopts its characteristic tetrahedral
geometry; the connectivity is indicated by the f ormula HO–O–S(O) 2–OH. It is one of the strongest oxidants know n
(E0 = +2.51 V) and is highly explosive.

H2SO5 is sometimes conf used w ith H2S2O8, know n as peroxydisulf uric acid. The disulf uric acid, w hich appears to
be more w idely used as its alkali metal salts, has the structure HO–S(O) 2–O–O–S(O) 2–OH.

Contents [hide]
1 History
2 Synthesis and production
3 Uses in industry
4 Hazards
5 See also
6 References
Names
IUPAC names
Peroxy sulf uric acid
History [ edit ]
Sulf uroperoxoic acid[1]
H2SO5 w as f irst described in 1898 by Heinrich Caro, af ter w hom it is named.[3] Sy stematic IUPAC name
(Dioxidanido)hy droxidodioxidosulf ur[1][2]
Other names
Synthesis and production [ edit ]
Peroxosulf uric acid[1]
The laboratory scale preparation of Caro's acid involves the combination of chlorosulf uric acid and hydrogen Peroxomonosulf uric acid[citation needed]
Persulf uric acid[citation needed]
peroxide.
Identifiers
H2O2 + ClSO2OH ⇌ H2SO5 + HCl [4] CAS Number 10361-76-9
Published patents include more than one reaction f or preparation of Caro's acid, usually as an intermediate f or the 3D model (JSmol) Interactiv e image
production of potassium monopersulf ate (PMPS), a bleaching and oxidizing agent. One patent f or production of Interactiv e image

Caro's acid f or this purpose gives the f ollow ing reaction: ChEBI CHEBI:29286
ChemSpider 2035480
H2O2 + H2SO4 ⇌ H2SO5 + H2O [5]
ECHA Inf oCard 100.028.879
EC Number 231-766-6
Uses in industry [ edit ] Gmelin Ref erence 101039

H2SO5 has been used f or a variety of disinf ectant and cleaning applications, e.g., sw imming pool treatment and PubChem CID 2754594

denture cleaning. Alkali metal salts of H2SO5 show promise f or the delignif ication of w ood.[6] UN number 1483
InChI [show]
Ammonium, sodium, and potassium salts of H2SO5 are used in the plastic industry as polymerization initiators,
SMILES [show]
etchants, desizing agents, soil conditioner, and f or decolorizing and deodorizing oils.
Properties
Potassium peroxymonosulf ate, KHSO5, is the potassium acid salt of peroxymonosulf uric acid. It is w idely used as Chemical f ormula H 2SO5
an oxidizing agent. Molar mass 114.078 g mol−1
Appearance White cry stals
Hazards [ edit ] Density 2.239 g cm −3
Conjugate base Peroxomonosulf ate
Pure Caro's acid is highly explosive. Explosions have been reported at Brow n University [7] and Sun Oil. As w ith all
Structure
strong oxidizing agents, peroxysulf uric acid should be kept aw ay f rom organic compounds such as ethers and
Coordination Tetrahedral at S
ketones because of its ability to peroxidize these compounds, creating highly unstable molecules such as acetone geometry
peroxide. Hazards
Main hazards strong oxidizer
See also [ edit ] Except where otherwise noted, data are giv en
f or materials in their standard state (at 25 °C
Peroxydisulf uric acid [77 °F], 100 kPa).

Peroxomonosulf ate v erif y (what is ?)


Inf obox ref erences

References [ edit ]

1. ^ a b c International Union of Pure and Applied Chemistry (2005). Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005). Cambridge (UK): RSC–IUPAC.
ISBN 0-85404-438-8. p. 139. Electronic v ersion.
2. ^ "peroxy sulf uric acid (CHEBI:29286)" . Chemical Entities of Biological Interest. UK: European Bioinf ormatics Institute. 20 Nov ember 2007. Retriev ed 17 Nov ember 2011.
3. ^ Caro, H. (1898). "Zur Kenntniss der Oxy dation aromatischer Amine" [[Contribution] to [our] knowledge of the oxidation of aromatic amines]. Zeitschrift für angewandte
Chemie. 11 (36): 845–846. doi:10.1002/ange.18980113602 .
4. ^ "Sy nthesis of Caro's acid" . PrepChem.com. 2017-02-13. Retriev ed 2018-10-12.
5. ^ A method and apparatus for producing a peroxyacid solution , retriev ed 2018-10-12
6. ^ Springer, E. L.; McSweeny, J. D. (1993). "Treatment of sof twood kraf t pulps with peroxy monosulf ate bef ore oxy gen delignif ication" . Tappi Journal. 76 (8): 194–199.
ISSN 0734-1415 .
7. ^ J.O. Edwards (1955). "SAFETY". Chem. Eng. News. 33 (32): 3336. doi:10.1021/cen-v 033n032.p3336 .

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