CAS Number 127-09-3
·
Linear Formula CH3COONa
·
Molecular Weight 82.03
·
Beilstein Registry
Number 3595639
·
EC Number 204-823-8
·
MDL number MFCD00012459
·
PubChem Substance ID 57654611
·
eCl@ss 39021906
Sodium acetate, CH3COONa, also abbreviated NaOAc,[8] also known as sodium ethanoate, is the sodium salt of acetic acid. This colorless deliquescent salt has a wide
range of uses.
Detailed description
Applications
Industrial
Sodium acetate is used in the textile industry to
neutralize sulfuric
acid waste streams and also as a photoresist while using aniline
dyes. It is also a pickling agent in chrome tanning and helps to impede vulcanization of chloroprene in synthetic
rubber production. In processing cotton for disposable cotton pads,
sodium acetate is used to eliminate the buildup of static electricity.
Concrete longevity
Sodium acetate is used to mitigate water damage to
concrete by acting as a concrete sealant, while also being environmentally benign and cheaper than the
commonly used epoxy alternative for
sealing concrete against water permeation.[9]
Food
Sodium acetate may be added to food as a seasoning,
sometimes in the form of sodium
diacetate, a one-to-one complex of sodium acetate and acetic
acid,[10] given the E-number E262. It is often used to give potato chips a salt
and vinegar flavor.
Buffer solution
As the conjugate base of acetic
acid, a solution of sodium acetate and acetic acid can
act as a buffer to keep a relatively
constant pH level. This is useful especially in biochemical applications where
reactions are pH-dependent in a mildly acidic range (pH 4-6).
Heating pad
Sodium acetate is also used in heating
pads, hand
warmers, and hot ice. Sodium acetate trihydrate crystals
melt at 136.4 °F/58 °C[11] (to 137.12 °F/58.4 °C),[12] dissolving in their water of crystallization. When they are heated past the melting point and subsequently
allowed to cool, the aqueous solution becomes supersaturated. This solution is capable of cooling to room temperature
without forming crystals. By pressing on a metal disc within the heating pad, a nucleation center is formed,
causing the solution to crystallize back into solid sodium acetate trihydrate.
The bond-forming process of crystallization is exothermic.[13][14]The latent heat of fusion is about
264–289 kJ/kg.[11] Unlike some types of
heat packs, such as those dependent upon irreversible chemical reactions, a
sodium acetate heat pack can be easily reused by immersing the pack in boiling
water for a few minutes, until the crystals are completely dissolved, and
allowing the pack to slowly cool to room temperature.[15]
Preparation
For laboratory use, sodium acetate is inexpensive
and usually purchased instead of being synthesized. It is sometimes produced in
a laboratory experiment by the reaction of acetic
acid, commonly in the 5–8% solution known as vinegar, with sodium
carbonate ("washing soda"), sodium bicarbonate ("baking
soda"), or sodium
hydroxide ("lye"). Any of these reactions produce sodium acetate
and water. When a sodium and carbonate ion-containing compound is used as the
reactant, the carbonate anion from sodium bicarbonate or carbonate, reacts with
hydrogen from the carboxyl group (-COOH) in acetic acid, forming carbonic
acid. Carbonic acid readily decomposes under normal
conditions into gaseous carbon dioxide and water. This is the reaction taking
place in the well-known "volcano" that occurs when the household
products, baking soda and vinegar, are combined.
CH3COOH + NaHCO3 → CH3COONa + H2CO
3
3
H2CO
3 → CO
2 + H
2O
3 → CO
2 + H
2O
Industrially, sodium acetate is prepared from glacial acetic acid and sodium
hydroxide.
CH3COOH
+ NaOH → CH3COONa + H2O
PRICE
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