Sodium dichromate

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Sodium dichromate

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EC Number	Template:Unbulleted list
Template:Longitem	21597
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UN number	3288
Template:Longitem	Na2Cr2O7
Molar mass	261.97 g/mol (anhydrous) 298.00 g/mol (dihydrate)
Appearance	bright orange
Odor	odorless
Density	2.52 g/cm3
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Solubility in other solvents	soluble in methanol, ethanol
Template:Longitem	1.661 (dihydrate)
NFPA 704 (fire diamond)	Template:NFPA 704 diamond
Template:Longitem	Sodium chromate Sodium molybdate Sodium tungstate
Template:Longitem	Potassium dichromate Ammonium dichromate

Sodium dichromate is the inorganic compound with the formula Na₂Cr₂O₇. However, the salt is usually handled as its dihydrate Na₂Cr₂O₇·2H₂O. Virtually all chromium ore is processed via conversion to sodium dichromate and virtually all compounds and materials based on chromium are prepared from this salt. In terms of reactivity and appearance, sodium dichromate and potassium dichromate are very similar. The sodium salt is, however, around twenty times more soluble in water than the potassium salt (49 g/L at 0 °C) and its equivalent weight is also lower, which is often desirable.

Preparation

Sodium dichromate is generated on a large scale from ores containing chromium(III) oxides. The ore is fused with a base, typically sodium carbonate, at around 1000 °C in the presence of air (source of oxygen):

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This step solubilizes the chromium and allows it to be extracted into hot water. At this stage, other components of the ore such as aluminium and iron compounds, are poorly soluble. Acidification of the resulting aqueous extract with sulfuric acid or carbon dioxide affords the dichromate:

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The dichromate is isolated as the dihydrate by crystallization. In this way, many millions of kilograms of sodium dichromate are produced annually.

Since chromium(VI) is toxic, especially as the dust, such factories are subject to stringent regulations. For example, effluent from such refineries is treated with reducing agents to return any chromium(VI) to chromium(III), which is less threatening to the environment. A variety of hydrates of this salt are known, ranging from the decahydrate below 19.5 °C (CAS# 13517-17-4 ) as well as hexa-, tetra-, and dihydrates. Above 62 °C, these salts lose water spontaneously to give the anhydrous material. It is crystallised around 30 to 35 degrees C

Reactions

Dichromate and chromate salts are oxidizing agents. For the tanning of leather, sodium dichromate is first reduced with sulfur dioxide.

In the area of organic synthesis, this compound oxidizes benzylic and allylic C-H bonds to carbonyl derivatives. For example, 2,4,6-trinitrotoluene is oxidized to the corresponding carboxylic acid. Similarly, 2,3-dimethylnaphthalene is oxidized by Na₂Cr₂O₇ to 2,3-naphthalenedicarboxylic acid.

Secondary alcohols are oxidized to the corresponding ketone, e.g. menthol to menthone; dihydrocholesterol to cholestanone:

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Relative to the potassium salt, the main advantage of sodium dichromate is its greater solubility in water and polar solvents like acetic acid.

For hexavalent chrome plating, chromate is converted to the so-called chromic acid (essentially chromium trioxide) by sulfuric acid.

Sodium dichromate can be used in fluorene to fluorenone conversion.

Safety

Like all hexavalent chromium compounds, sodium dichromate is carcinogenic. The compound is also corrosive and exposure may produce severe eye damage or blindness. Human exposure further encompasses impaired fertility, heritable genetic damage and harm to unborn children.