Sodium sulfite
















































































































































Sodium sulphite

Sodium sulfite

Sodium sulfite ball-and-stick.png





Sodium sulfite.jpg

anhydrous


Sodium sulfite hydrate.jpg

hydrate


Names

IUPAC name
Sodium sulfite

Other names
Hypo clear (photography)
E221

Identifiers

CAS Number



  • 7757-83-7 ☑Y


3D model (JSmol)


  • Interactive image


ChEBI


  • CHEBI:86477 ☒N


ChemSpider


  • 22845 ☑Y


ECHA InfoCard

100.028.929

EC Number
231-821-4

E number
E221 (preservatives)


PubChem CID


  • 24437


RTECS number
WE2150000

UNII


  • VTK01UQK3G ☑Y





Properties

Chemical formula

Na2SO3

Molar mass
126.043 g/mol
Appearance
White solid

Odor
Odorless

Density
2.633 g/cm3 (anhydrous)
1.561 g/cm3 (heptahydrate)

Melting point
33.4 °C (92.1 °F; 306.5 K) (dehydration of heptahydrate)
500 °C (anhydrous)

Boiling point
Decomposes

Solubility in water

27.0 g/100mL water (20 °C)

Solubility
Soluble in glycerol
Insoluble in ammonia, chlorine

log P
−4

Acidity (pKa)
~9 (heptahydrate)


Refractive index (nD)

1.565
Structure

Crystal structure

Hexagonal (anhydrous)
Monoclinic (heptahydrate)
Hazards

Safety data sheet

ICSC 1200

NFPA 704



Flammability code 0: Will not burn. E.g., water
Health code 2: Intense or continued but not chronic exposure could cause temporary incapacitation or possible residual injury. E.g., chloroform
Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen
Special hazards (white): no code
NFPA 704 four-colored diamond


0


2


0



Flash point
Non-flammable
Related compounds

Other anions


Sodium selenite

Other cations


Potassium sulfite

Related compounds


Sodium bisulfite
Sodium metabisulfite
Sodium sulfate

Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).


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Infobox references



Sodium sulfite (sodium sulphite) is a soluble sodium salt of sulfurous acid (sulfite) with the chemical formula Na2SO3. It is also used as a preservative to prevent dried fruit from discoloring, and for preserving meats, and is used in the same way as sodium thiosulfate to convert elemental halogens to their respective hydrohalic acids, in photography and for reducing chlorine levels in pools. In boiler systems, sulfite and bisulfite are the most commonly employed oxygen scavengers used to prevent pitting corrosion. Sodium sulfite is also a byproduct of sulfur dioxide scrubbing, a part of the flue-gas desulfurization process.




Contents






  • 1 Preparation


  • 2 Applications


  • 3 Reactions


  • 4 Descriptive chemistry


  • 5 References





Preparation


Sodium sulfite can be prepared in lab by reacting sodium hydroxide solution with sulfur dioxide gas:


2 NaOH + SO2 → Na2SO3 + H2O

Evolution of SO2 by adding few drops of concentrated hydrochloric acid will indicate if sodium hydroxide is nearly gone, turned to aqueous sodium sulfite:


Na2SO3 + 2 HCl → 2 NaCl + SO2 + H2O

Sodium sulfite is made industrially by reacting sulfur dioxide with a solution of sodium carbonate. The initial combination generates sodium bisulfite (NaHSO3), which is converted to the sulfite by reaction with sodium hydroxide or sodium carbonate.[1]


The overall reaction is:


SO2 + Na2CO3 → Na2SO3 + CO2


Applications


Sodium sulfite is primarily used in the pulp and paper industry. It is used in water treatment as an oxygen scavenger agent, to treat water being fed to steam boilers to avoid corrosion problems,[2] in the photographic industry to protect developer solutions from oxidation and (as hypo clear solution) to wash fixer (sodium thiosulfate) from film and photo-paper emulsions, in the textile industry as a bleaching, desulfurizing and dechlorinating agent and in the leather trade for the sulphonation of tanning extracts. It is used in the purification of TNT for military use. It is used in chemical manufacturing as a sulfonation and sulfomethylation agent. It is used in the production of sodium thiosulfate. It is used in other applications, including froth flotation of ores, oil recovery, food preservatives, and making dyes.



Reactions


Sodium sulfite forms a bisulfite adduct with aldehydes, and with ketones forms a sulfonic acid. It is used to purify or isolate aldehydes and ketones.



Descriptive chemistry


Sodium sulfite is decomposed by even weak acids, giving up sulfur dioxide gas.


Na2SO3 + 2 H+ → 2 Na+ + H2O + SO2

A saturated aqueous solution has pH of ~9. Solutions exposed to air are eventually oxidized to sodium sulfate. If sodium sulfite is allowed to crystallize from aqueous solution at room temperature or below, it does so as a heptahydrate. The heptahydrate crystals effloresce in warm dry air. Heptahydrate crystals also oxidize in air to form the sulfate. The anhydrous form is much more stable against oxidation by air.[3]



References





  1. ^ Weil, Edward D.; Sandler, Stanley R. (1999). "Sulfur Compounds". In Kroschwitz, Jacqueline I. Kirk-Othmer Concise Encylclopedia of Chemical Technology (4th ed.). New York: John Wiley & Sons, Inc. p. 1937. ISBN 978-0471419617..mw-parser-output cite.citation{font-style:inherit}.mw-parser-output .citation q{quotes:"""""""'""'"}.mw-parser-output .citation .cs1-lock-free a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/6/65/Lock-green.svg/9px-Lock-green.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-limited a,.mw-parser-output .citation .cs1-lock-registration a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/d/d6/Lock-gray-alt-2.svg/9px-Lock-gray-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .citation .cs1-lock-subscription a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/a/aa/Lock-red-alt-2.svg/9px-Lock-red-alt-2.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration{color:#555}.mw-parser-output .cs1-subscription span,.mw-parser-output .cs1-registration span{border-bottom:1px dotted;cursor:help}.mw-parser-output .cs1-ws-icon a{background:url("//upload.wikimedia.org/wikipedia/commons/thumb/4/4c/Wikisource-logo.svg/12px-Wikisource-logo.svg.png")no-repeat;background-position:right .1em center}.mw-parser-output code.cs1-code{color:inherit;background:inherit;border:inherit;padding:inherit}.mw-parser-output .cs1-hidden-error{display:none;font-size:100%}.mw-parser-output .cs1-visible-error{font-size:100%}.mw-parser-output .cs1-maint{display:none;color:#33aa33;margin-left:0.3em}.mw-parser-output .cs1-subscription,.mw-parser-output .cs1-registration,.mw-parser-output .cs1-format{font-size:95%}.mw-parser-output .cs1-kern-left,.mw-parser-output .cs1-kern-wl-left{padding-left:0.2em}.mw-parser-output .cs1-kern-right,.mw-parser-output .cs1-kern-wl-right{padding-right:0.2em}


  2. ^ "Pre-boiler and Boiler Corrosion Control | GE Water".


  3. ^ Merck Index of Chemicals and Drugs, 9th ed. monograph 8451










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