Performic acid

From Wikipedia, the free encyclopedia
Jump to navigation Jump to search

<templatestyles src="Chembox/styles.css"/>

Template:Chembox AllOtherNamesTemplate:Chembox headerbarTemplate:Chembox IndexlistTemplate:Chembox JmolTemplate:Chembox ChEMBLTemplate:Chembox ECHATemplate:Chembox E numberTemplate:Chembox IUPHAR ligandTemplate:Chembox UNIITemplate:Chembox CompToxTemplate:Chembox headerbarTemplate:Chembox HazardsTemplate:Chembox Datapage checkTemplate:Yesno
Performic acid
Template:Chembox image sbs cell
Template:Longitem Template:Unbulleted list
ChEBI Template:Unbulleted list
ChemSpider Template:Unbulleted list
DrugBank Template:Unbulleted list
EC Number Template:Unbulleted list
KEGG Template:Unbulleted list
Template:Longitem Template:Unbulleted list
RTECS number Template:Unbulleted list
Script error: No such module "collapsible list".
Script error: No such module "collapsible list".
Template:Longitem Template:Chembox Elements/molecular formula
Molar mass Template:Chem molar mass
Appearance Colorless liquid
Melting point Template:Chembox CalcTemperatures
Boiling point Template:Chembox CalcTemperatures
Acidity (pKa) 7.1[2][3]

Template:Chembox Footer/tracking container onlyScript error: No such module "TemplatePar".Template:Short description

Performic acid (PFA) is an organic compound with the formula CH2O3. It is an unstable colorless liquid which can be produced by mixing formic acid with hydrogen peroxide. Owing to its oxidizing and disinfecting action, it is used in the chemical, medical and food industries.

Properties and applications

Performic acid is a colorless liquid soluble in water, alcohols, ether, benzene, chloroform and other organic solvents.[4][5] Its strong oxidizing properties are used for cleaving disulfide bonds in protein mapping,[6] as well as for epoxidation, hydroxylation[7] and oxidation reactions in organic synthesis.[5] In the medical and food industries, performic acid is commonly used to disinfect equipment. It is effective against viruses, bacterial spores, algae, microscopic fungi and mycobacteria, as well as other microorganisms such as zooplankton.

The popularity of performic acid as a sterilizer originates from the safe nature of its degradation products, mostly carbon dioxide, oxygen and water.[4][8] The disinfecting action of performic acid is also faster than that of the related compounds peracetic acid and hydrogen peroxide.[9] The major drawbacks of performic acid are handling dangers related to its high reactivity, as well as instability, especially upon heating, which means that the acid must be used within about 12 hours of it being synthesised.[9][10][11]

Synthesis

Performic acid is synthesized by the reaction of formic acid and hydrogen peroxide by the following equilibrium reaction:

Synthesis of Performic acid
Synthesis of Performic acid

Synthesis of pure performic acid has not been reported, but aqueous solutions up to about 48% can be formed by simply mixing equimolar amounts of concentrated aqueous reactant solutions.[4] Using an excess of either reactant shifts the equilibrium towards the product side. The aqueous product solution can be distilled to increase the concentration of performic acid to about 90%.[4]

This reaction is reversible and can be used for large scale industrial production if accelerated with a catalyst; however, its temperature must be kept below 80–85 °C to avoid an explosion.[12] The catalyst can be nitric, hydrofluoric, phosphoric or sulfuric acid or their salts;[4][13] it can also be an organic compound containing at least one ester group, such as carboxylic acid ester[14] or peracetic acid.[9]

Safety

Performic acid is non-toxic; it does irritate the skin, but less so than peracetic acid. Concentrated acid (above 50%) is highly reactive; it readily decomposes upon heating, and explodes upon rapid heating to 80–85 °C. It may ignite or explode at room temperature when combined with flammable substances, such as formaldehyde, benzaldehyde, or aniline, and explodes violently upon addition of metal powders.[4] For this reason, spilled performic acid is diluted with cold water and collected with neutral, non-flammable inorganic absorbents, such as vermiculite.[5]

References

<templatestyles src="Reflist/styles.css" />

  1. Script error: No such module "citation/CS1".
  2. a b Cite error: Script error: No such module "Namespace detect".Script error: No such module "Namespace detect".
  3. F. A. Carroll Perspectives on Structure and Mechanism in Organic Chemistry, Wiley-Interscience, 2010, Template:ISBN p. 416
  4. a b c d e f Script error: No such module "Citation/CS1".
  5. a b c Pradyot Patnaik A comprehensive guide to the hazardous properties of chemical substances, Wiley-Interscience, 2007, Template:ISBN, p. 128
  6. Script error: No such module "Citation/CS1".
  7. Script error: No such module "Citation/CS1".
  8. Script error: No such module "Citation/CS1".
  9. a b c Preuss, A., Fuchs, R., Huss, M. & Schneider, R. 2001 Aqueous Disinfecting Agent Containing Performic Acid and Peracetic Acid Process for Production and Process for Use Thereof U.S. patent 6211237, Issue date: April 3, 2001
  10. Script error: No such module "Citation/CS1".
  11. Script error: No such module "Citation/CS1".
  12. Elvers, B. et al. (ed.) (1991) Ullmann's Encyclopedia of Industrial Chemistry, 5th ed. Vol. A12, Wiley, p. 16
  13. Script error: No such module "Citation/CS1".
  14. Matilla, T. and Aksela, R. 2000 Method for the Preparation of Aqueous Solutions Containing Performic Acid as Well as Their Use. U.S. patent 6049002, Issue date: April 11, 2000

Script error: No such module "Check for unknown parameters".