Peroxymonosulfuric acid

Last updated
Peroxymonosulfuric acid
Peroxomonoschwefelsaure.svg
Caro's-acid-3D-balls.png
Names
IUPAC names
Peroxysulfuric acid
Sulfuroperoxoic acid [1]
Systematic IUPAC name
(Dioxidanido)hydroxidodioxidosulfur [1] [2]
Other names
Peroxosulfuric acid [1]
Peroxomonosulfuric acid[ citation needed ]
Persulfuric acid[ citation needed ]
Caro's acid
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
ECHA InfoCard 100.028.879 OOjs UI icon edit-ltr-progressive.svg
EC Number
  • 231-766-6
101039
PubChem CID
UNII
UN number 1483
  • InChI=1S/H2O5S/c1-5-6(2,3)4/h1H,(H,2,3,4) Yes check.svgY
    Key: FHHJDRFHHWUPDG-UHFFFAOYSA-N Yes check.svgY
  • OOS(O)(=O)=O
  • [O].[O].OOSO
Properties
H
2
SO
5
Molar mass 114.078 g mol−1
AppearanceWhite crystals
Density 2.239 g cm−3
Melting point 45 °C
Acidity (pKa)1, 9.3 [3]
Conjugate base Peroxomonosulfate
Structure
Tetrahedral at S
Hazards
Occupational safety and health (OHS/OSH):
Main hazards
strong oxidizer
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
X mark.svgN  verify  (what is  Yes check.svgYX mark.svgN ?)

Peroxymonosulfuric acid, also known as persulfuric acid, peroxysulfuric acid is the inorganic compound with the formula H2SO5. It is a white solid. It is a component of Caro's acid, which is a solution of peroxymonosulfuric acid in sulfuric acid containing small amounts of water. [4] Peroxymonosulfuric acid is a very strong oxidant (E0  = +2.51 V).

Contents

Structure

In peroxymonosulfuric acid, the S(VI) center adopts its characteristic tetrahedral geometry; the connectivity is indicated by the formula HO–O–S(O)2–OH. The S-O-H proton is more acidic. [4]

History

The German chemist Heinrich Caro first reported investigations of mixtures of hydrogen peroxide and sulfuric acid. [5]

Synthesis and production

One laboratory scale preparation of Caro's acid involves the combination of chlorosulfuric acid and hydrogen peroxide: [6]

H2O2 + ClSO2OH ⇌ H2SO5 + HCl

Patents include more than one reaction for preparation of Caro's acid, usually as an intermediate for the production of potassium monopersulfate (PMPS), a bleaching and oxidizing agent. One route employs the following reaction: [7]

H2O2 + H2SO4 ⇌ H2SO5 + H2O

This reaction is related to "piranha solution".

Uses in industry

H
2
SO
5
and Caro's acid have been used for a variety of disinfectant and cleaning applications, e.g., swimming pool treatment and denture cleaning. It is used in gold mining to destroy the cyanide in the waste stream ("Tailings").

Alkali metal salts of H
2
SO
5
, especially oxone, are widely investigated.

Hazards

These peroxy acids can be explosive. Explosions have been reported at Brown University [8] and Sun Oil. As with all strong oxidizing agents, peroxysulfuric acid is incompatible with organic compounds.

See also

Related Research Articles

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Hydrogen peroxide is a chemical compound with the formula H2O2. In its pure form, it is a very pale blue liquid that is slightly more viscous than water. It is used as an oxidizer, bleaching agent, and antiseptic, usually as a dilute solution in water for consumer use and in higher concentrations for industrial use. Concentrated hydrogen peroxide, or "high-test peroxide", decomposes explosively when heated and has been used as both a monopropellant and an oxidizer in rocketry.

<span class="mw-page-title-main">Redox</span> Chemical reaction in which oxidation states of atoms are changed

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2
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2
is for dry-cell batteries, such as the alkaline battery and the zinc–carbon battery. MnO
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is also used as a pigment and as a precursor to other manganese compounds, such as KMnO
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. It is used as a reagent in organic synthesis, for example, for the oxidation of allylic alcohols. MnO
2
has an α-polymorph that can incorporate a variety of atoms in the "tunnels" or "channels" between the manganese oxide octahedra. There is considerable interest in α-MnO
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Hydrobromic acid is an aqueous solution of hydrogen bromide. It is a strong acid formed by dissolving the diatomic molecule hydrogen bromide (HBr) in water. "Constant boiling" hydrobromic acid is an aqueous solution that distills at 124.3 °C (255.7 °F) and contains 47.6% HBr by mass, which is 8.77 mol/L. Hydrobromic acid is one of the strongest mineral acids known.

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<span class="mw-page-title-main">Potassium peroxymonosulfate</span> Chemical compound

Potassium peroxymonosulfate is widely used as an oxidizing agent, for example, in pools and spas. It is the potassium salt of peroxymonosulfuric acid. Potassium peroxymonosulfate per se is rarely encountered. It is often confused with the triple salt 2KHSO5·KHSO4·K2SO4, known as Oxone.

<span class="mw-page-title-main">Sodium sulfide</span> Chemical compound

Sodium sulfide is a chemical compound with the formula Na2S, or more commonly its hydrate Na2S·9H2O. Both the anhydrous and the hydrated salts in pure crystalline form are colorless solids, although technical grades of sodium sulfide are generally yellow to brick red owing to the presence of polysulfides and commonly supplied as a crystalline mass, in flake form, or as a fused solid. They are water-soluble, giving strongly alkaline solutions. When exposed to moisture, Na2S immediately hydrates to give sodium hydrosulfide.

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Piranha solution, also known as piranha etch, is a mixture of sulfuric acid and hydrogen peroxide. The resulting mixture is used to clean organic residues off substrates, for example silicon wafers. Because the mixture is a strong oxidizing agent, it will decompose most organic matter, and it will also hydroxylate most surfaces, making them highly hydrophilic (water-compatible). This means the solution can also easily dissolve fabric and skin, potentially causing severe damage and chemical burns in case of inadvertent contact. It is named after the piranha fish due to its tendency to rapidly dissolve and 'consume' organic materials through vigorous chemical reactions.

Peracetic acid (also known as peroxyacetic acid, or PAA) is an organic compound with the formula CH3CO3H. This peroxy acid is a colorless liquid with a characteristic acrid odor reminiscent of acetic acid. It can be highly corrosive.

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3
H
. It is one of the unstable hydrogen polyoxides. In aqueous solutions, trioxidane decomposes to form water and singlet oxygen:

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<span class="mw-page-title-main">Metal peroxide</span>

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2
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References

  1. 1 2 3 International Union of Pure and Applied Chemistry (2005). Nomenclature of Inorganic Chemistry (IUPAC Recommendations 2005). Cambridge (UK): RSCIUPAC. ISBN   0-85404-438-8. p. 139. Electronic version.
  2. "Peroxysulfuric acid (CHEBI:29286)". Chemical Entities of Biological Interest. UK: European Bioinformatics Institute. 20 November 2007. Retrieved 17 November 2011.
  3. Perrin, D. D., ed. (1982) [1969]. Ionisation Constants of Inorganic Acids and Bases in Aqueous Solution. IUPAC Chemical Data (2nd ed.). Oxford: Pergamon (published 1984). Entry 176. ISBN   0-08-029214-3. LCCN   82-16524.
  4. 1 2 Jakob, Harald; Leininger, Stefan; Lehmann, Thomas; Jacobi, Sylvia; Gutewort, Sven (2007). "Peroxo Compounds, Inorganic". Ullmann's Encyclopedia of Industrial Chemistry. doi:10.1002/14356007.a19_177.pub2. ISBN   978-3-527-30673-2.
  5. Caro, H. (1898). "Zur Kenntniss der Oxydation 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.
  6. "Synthesis of Caro's acid". PrepChem.com. 2017-02-13. Retrieved 2018-10-12.
  7. A method and apparatus for producing a peroxyacid solution , retrieved 2018-10-12
  8. Edwards, J.O. (1955). "Safety". Chem. Eng. News . 33 (32): 3336. doi:10.1021/cen-v033n032.p3336.