Peroxymonosulfuric acid

{{Short description|Powerful oxidizing agent}}

{{Chembox

| Verifiedfields = changed

| Watchedfields = changed

| verifiedrevid = 464199379

| Name = Peroxymonosulfuric acid

| ImageFile = Peroxomonoschwefelsäure.svg

| ImageClass = skin-invert-image

| ImageFile_Ref = {{chemboximage|correct|??}}

| ImageName = Skeletal formula of peroxymonosulfuric acid

| ImageFile1 = Caro's-acid-3D-balls.png

| ImageClass1 = bg-transparent

| ImageFile1_Ref = {{chemboximage|correct|??}}

| ImageName1 = Ball and stick model of peroxymonosulfuric acid

| IUPACNames = Peroxysulfuric acid
Sulfuroperoxoic acid{{RedBookRef|page=139}}

| SystematicName = (Dioxidanido)hydroxidodioxidosulfur{{Cite web|title = Peroxysulfuric acid (CHEBI:29286)|url = http://www.ebi.ac.uk/chebi/searchId.do?chebiId=CHEBI:29286|work = Chemical Entities of Biological Interest|publisher = European Bioinformatics Institute|access-date = 17 November 2011|location = UK|date = 20 November 2007}}

| OtherNames = Peroxosulfuric acid
Peroxomonosulfuric acid{{Citation needed|date = November 2011}}

Persulfuric acid{{Citation needed|date = November 2011}}
Caro's acid

|Section1={{Chembox Identifiers

| CASNo = 7722-86-3

| CASNo_Ref = {{cascite|changed|CAS}}

| UNII_Ref = {{fdacite|correct|FDA}}

| UNII = JC6U8R2UJ9

| PubChem = 2754594

| ChemSpiderID = 2035480

| ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}}

| EINECS = 231-766-6

| UNNumber = 1483

| ChEBI = 29286

| ChEBI_Ref = {{ebicite|correct|EBI}}

| Gmelin = 101039

| SMILES = OOS(O)(=O)=O

| SMILES1 = [O].[O].OOSO

| StdInChI = 1S/H2O5S/c1-5-6(2,3)4/h1H,(H,2,3,4)

| StdInChI_Ref = {{stdinchicite|correct|chemspider}}

| StdInChIKey = FHHJDRFHHWUPDG-UHFFFAOYSA-N

| StdInChIKey_Ref = {{stdinchicite|correct|chemspider}}

}}

|Section2={{Chembox Properties

| Formula = {{Chem|H|2|SO|5}}

| MolarMass = 114.078 g mol−1

| Appearance = White crystals

| Density = 2.239 g cm−3

| ConjugateBase = Peroxomonosulfate

| pKa = 1, 9.3{{cite book|title=Ionisation Constants of Inorganic Acids and Bases in Aqueous Solution|editor-first=D. D.|editor-last=Perrin|edition=2nd|series=IUPAC Chemical Data|issue=29|publisher=Pergamon|location=Oxford|year=1982|publication-date=1984|orig-date=1969|lccn=82-16524|isbn=0-08-029214-3|at=Entry 176}}

| MeltingPt = 45 °C

}}

|Section3={{Chembox Structure

| Coordination = Tetrahedral at S

}}

|Section4={{Chembox Hazards

| MainHazards = strong oxidizer

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Peroxymonosulfuric acid, also known as persulfuric acid, peroxysulfuric acid is the inorganic compound with the formula {{chem2|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. Peroxymonosulfuric acid is a very strong oxidant (E0 = +2.51 V).

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.{{cite book |doi=10.1002/14356007.a19_177.pub2 |chapter=Peroxo Compounds, Inorganic |title=Ullmann's Encyclopedia of Industrial Chemistry |date=2007 |last1=Jakob |first1=Harald |last2=Leininger |first2=Stefan |last3=Lehmann |first3=Thomas |last4=Jacobi |first4=Sylvia |last5=Gutewort |first5=Sven |isbn=978-3-527-30673-2 }}

History

The German chemist Heinrich Caro first reported investigations of mixtures of hydrogen peroxide and sulfuric acid.{{cite journal |first=H. |last=Caro |year=1898 |title=Zur Kenntniss der Oxydation aromatischer Amine |trans-title=[Contribution] to [our] knowledge of the oxidation of aromatic amines |journal=Zeitschrift für angewandte Chemie |volume=11 |issue=36 |pages=845–846 |url=http://babel.hathitrust.org/cgi/pt?id=mdp.39015073166319;view=1up;seq=855 |doi=10.1002/ange.18980113602 |url-access=subscription }}

Synthesis and production

One laboratory scale preparation of Caro's acid involves the combination of chlorosulfuric acid and hydrogen peroxide:{{Cite web |url=http://www.prepchem.com/synthesis-caros-acid/ |title=Synthesis of Caro's acid |date=2017-02-13 |website=PrepChem.com |language=en-US |access-date=2018-10-12}}

:{{chem2 | 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:{{Citation |title=A method and apparatus for producing a peroxyacid solution |url=https://patents.google.com/patent/WO2005016511A1/da |access-date=2018-10-12}}

:{{chem2 | H2O2 + H2SO4 <-> H2SO5 + H2O }}

This reaction is related to "piranha solution".

Uses in industry

{{Chem|H|2|S|O|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 {{Chem|H|2|S|O|5}}, especially oxone, are widely investigated.

Hazards

These peroxy acids can be explosive. Explosions have been reported at Brown University{{cite journal | last1 = Edwards | first1 = J.O. | journal = Chem. Eng. News | volume = 33 | pages = 3336 | year = 1955 | doi = 10.1021/cen-v033n032.p3336 | title = Safety | issue = 32}} and Sun Oil. As with all strong oxidizing agents, peroxysulfuric acid is incompatible with organic compounds.

See also

References