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Chromium(III) sulfate

Chromium(III) sulfate
Chromium(III) sulfate.jpg
Names
IUPAC name
Chromium(III) sulfate
Other names
Basic chromium sulfate, chromic sulfate
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.030.217
PubChem CID
UNII
Properties
Cr2(SO4)3 • 12H2O
Molar mass 392.16 g/mol
608.363 g/mol (dodecahydrate)

716.45 g/mol (octadecahydrate)

Appearance reddish-brown crystals (anhydrous), purple crystals (hydrated)
Density 3.10 g/cm3 (anhydrous)
1.86 g/cm3 (pentadecahydrate)
1.709 g/cm3 (octadecahydrate)
Melting point 90 °C
Boiling point decomposes to chromic acid
insoluble (anhydrous)
soluble (hydrated)
Solubility soluble in alcohol
practically insoluble in acid
+11,800·10−6 cm3/mol
Hazards
Safety data sheet MSDS
NFPA 704
Flammability code 0: Will not burn. E.g., water Health code 1: Exposure would cause irritation but only minor residual injury. E.g., turpentine Reactivity code 0: Normally stable, even under fire exposure conditions, and is not reactive with water. E.g., liquid nitrogen Special hazards (white): no codeNFPA 704 four-colored diamond
Flash point Non-flammable
US health exposure limits (NIOSH):
PEL (Permissible)
TWA 1 mg/m3
REL (Recommended)
TWA 0.5 mg/m3
IDLH (Immediate danger)
250 mg/m3
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

716.45 g/mol (octadecahydrate)

Chromium(III) sulfate usually refers to the inorganic compounds with the formula Cr2(SO4)3.x(H2O), where x can range from 0 to 18. Additionally, ill-defined but commercially important "basic chromium sulfates" are known. These salts are usually either violet or green solids that are soluble in water.

Three chromium(III) sulfates are well characterized:

A variety of other chromium(III) sulfates are known, but also contain hydroxide or oxide ligands. Most important commercially is basic chromium sulfate, which is thought to be [Cr2(H2O)6(OH)4]SO4 (CAS#39380-78-4). It results from the partial neutralization of the hexahydrates. It is associated with environmental damage. Other chromium(III) hydroxides have been reported.

The most useful source of chromium(III) sulfate are the Cr(III) wastes from the chromate oxidation of various organic compounds. Anthroquinone and quinone are produced by on large scale by treatment of anthracene and phenol with chromic acid. A chromium(III) oxide coproduct is generated which is readily extracted into sulfuric acid. Evaporation of these acidic solutions affords the hydrate salt described above. The hydrated salts of chromium sulfate can also be produced, albeit impure, by extraction of various other chromium compounds, but these routes are not economically viable.. Extraction of chromite ore with sulfuric acid in the presence of some chromate gives solutions of chromium(III) sulfate contaminated with other metal ions. Similarly, dissolution of chrome alloys gives chromium sulfate together with ferrous sulfate.

Basic chromium sulfate is produced from chromate salts by reduction with sulfur dioxide, although other methods exist. The reduction could formally be written:

Since 33% of the anion charges are due to hydroxy ions the basicity is 33% (but in tanning jargon it is known as 33% reduced). Products with higher basicities, e.g. 42 or 50% may be obtained by the addition of sodium carbonate, these are often used in combination with sodium formate. The sodium sulfate is often left in the technical product since it is inert with respect to the tanning process. It is important to fully reduce the hexavalent chromium to trivalent since the hexavalent is more likely to cause health problems for tanners and leather consumers.


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