Sodium percarbonate
Names | |
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IUPAC name
sodium carbonate—hydrogen peroxide (2/3)
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Other names
sodium carbonate sesquiperhydrate, PCS, SPC, solid hydrogen peroxide, Sodium carbonate hydrogen peroxide, sodium carbonate peroxyhydrate
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.036.082 |
EC Number |
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PubChem CID
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RTECS number |
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
Na2CO3·1.5 H2O2 | |
Molar mass | 156.982 g/mol |
Appearance | white solid |
150 g/l | |
Hazards | |
Occupational safety and health (OHS/OSH): | |
Main hazards
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Irritant, Oxidizer |
Flash point | Non-flammable |
Related compounds | |
Other anions
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Sodium carbonate Sodium bicarbonate |
Other cations
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Calcium percarbonate Magnesium percarbonate |
Related compounds
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Sodium perborate Sodium persulfate Sodium perphosphate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Sodium percarbonate is a chemical substance with formula Na
2H
3CO
6. It is an adduct of sodium carbonate ("soda ash" or "washing soda") and hydrogen peroxide (that is, a perhydrate) whose formula is more properly written as 2 Na
2CO
3 · 3 H
2O
2. It is a colorless, crystalline, hygroscopic and water-soluble solid.[1] It is sometimes abbreviated as SPC. It contains 32.5% by weight of hydrogen peroxide.
The product is used in some eco-friendly bleaches and other cleaning products, and as a laboratory source of anhydrous hydrogen peroxide.
History
Sodium percarbonate was first prepared in 1899 by Russian Empire's chemist Sebastian Moiseevich Tanatar (Template:Lang-ru) (7 October 1849, Odessa – 30 November 1917, Odessa).[2]
Structure
At room temperature, solid sodium percarbonate has the orthorhombic crystal structure, with the Cmca crystallographic space group. The structure changes to Pbca as the crystals are cooled below about −30 °C.[3]
Chemistry
Dissolved in water, sodium percarbonate yields a mixture of hydrogen peroxide (which eventually decomposes to water and oxygen), sodium cations Na+
, and carbonate CO2−
3.[1][4]
Production
Sodium percarbonate is produced industrially by crystallization of a solution of sodium carbonate and hydrogen peroxide, with proper control of the pH and concentrations.[5][3][6] This is also a convenient laboratory method.
Alternatively, dry sodium carbonate may be treated directly with concentrated hydrogen peroxide solution.[7]
World production capacity of this compound was estimated at several hundred thousand tons for 2004.[8]
Uses
As an oxidizing agent, sodium percarbonate is an ingredient in a number of home and laundry cleaning products, including non-chlorine bleach products such as Oxyper, OxiClean, Tide laundry detergent,[1] and Vanish.[4]
Many commercial products mix a percentage of sodium percarbonate with sodium carbonate. The average percentage of an "Oxy" product in the supermarket is 65% sodium percarbonate and 35% sodium carbonate. The "ultra boosters" seen on infomercials may contain as much as 80% sodium percarbonate. However, sodium percarbonate is less expensive in its pure form [citation needed] and can be adjusted to any percentage the user desires.
Sodium percarbonate can be used in organic synthesis as a convenient source of anhydrous H2O2, in particular in solvents that cannot dissolve the carbonate but can leach the H2O2 out of it.[9] A method for generating trifluoroperacetic acid in situ for use in Baeyer–Villiger oxidations from sodium percarbonate and trifluoroacetic anhydride has been reported; it provides a convenient and cheap approach to this reagent without the need to obtain highly concentrated hydrogen peroxide.[10][11]
References
- ^ a b c Craig W. Jones (1999). Applications of hydrogen peroxide and its derivatives. Royal Society of Chemistry. ISBN 0-85404-536-8.
- ^ S. Tanatar (1899) "Percarbonate", Berichte der Deutschen chemischen Gesellschaft zu Berlin, 32 : 1544–1546.
- ^ a b
R. G. Pritchard; E. Islam (2003). "Sodium percarbonate between 293 and 100 K". Acta Crystallographica Section B. B59 (5): 596–605. doi:10.1107/S0108768103012291. PMID 14586079.
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: Unknown parameter|lastauthoramp=
ignored (|name-list-style=
suggested) (help) - ^ a b "Oxygen-based bleaches Archived 2012-01-24 at the Wayback Machine", The Royal Society of Chemistry, and Reckitt Benckiser (the manufacturers of Vanish).
- ^ J. M. Adams and R. G. Pritchard (1977): "The crystal structure of sodium percarbonate: an unusual layered solid". Acta Crystallographica Section B, volume B33, issue 12, pages 3650–3653. doi:10.1107/S0567740877011790
- ^ Alun P. James, Graham R. Horne, Richard Roesler, and others (1997): "Process for producing sodium percarbonate". US Patent US6231828B1, priority date 1997-03-26.
- ^ Sang Ryul Kim, Chong Yun Kwag, Hwan Kee Heo, Jong-Pill Lee (1996): "Process for manufacturing granular sodium percarbonate". US Patent US5851420A, priority date 1996-02-29
- ^ 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) - ^ McKillop, A (1995). "Sodium perborate and sodium percarbonate: Cheap, safe and versatile oxidising agents for organic synthesis". Tetrahedron. 51 (22): 6145–6166. doi:10.1016/0040-4020(95)00304-Q.
- ^ Kang, Ho-Jung; Jeong, Hee-Sun (1996). "New Method of Generating Trifluoroperoxyacetic acid for the Baeyer-Villiger Reaction". Bull. Korean Chem. Soc. 17 (1): 5–6.
- ^ Caster, Kenneth C.; Rao, A. Somasekar; Mohan, H. Rama; McGrath, Nicholas A.; Brichacek, Matthew (2012). "Trifluoroperacetic Acid". Encyclopedia of Reagents for Organic Synthesis. e-EROS Encyclopedia of Reagents for Organic Synthesis. doi:10.1002/047084289X.rt254.pub2. ISBN 978-0471936237.