French
DeutschSodium chromate
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| Names | |
|---|---|
| IUPAC name Sodium chromate | |
| Other names Chromic acid, (Na2CrO4), disodium salt Chromium disodium oxide Rachromate | |
| Identifiers | |
3D model (JSmol) | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.028.990 |
| EC Number |
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PubChem CID | |
| RTECS number |
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| UNII | |
| UN number | 3288 |
CompTox Dashboard (EPA) | |
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| Properties | |
| Na2CrO4 | |
| Molar mass | 161.97 g/mol |
| Appearance | yellow crystals |
| Odor | odorless |
| Density | 2.698 g/cm3 |
| Melting point | 792 °C (1,458 °F; 1,065 K) (anhydrous) 20 °C (decahydrate) |
| 31.8 g/100 mL (0 °C) 84.5 g/100 mL (25 °C) 126.7 g/100 mL (100 °C) | |
| Solubility | slightly soluble in ethanol |
| Solubility in methanol | 0.344 g/100 mL (25 °C) |
| +55.0·10−6 cm3/mol | |
| Structure | |
| orthorhombic (hexagonal above 413 °C) | |
| Thermochemistry | |
Heat capacity (C) | 142.1 J/mol K |
Std molar entropy (S⦵298) | 174.5 J/mol K |
Std enthalpy of formation (ΔfH⦵298) | −1329 kJ/mol |
Gibbs free energy (ΔfG⦵) | -1232 kJ/mol |
| Hazards | |
| GHS labelling: | |
     | |
| Danger | |
| H301, H312, H314, H317, H330, H334, H340, H350, H360, H372, H410 | |
| P201, P202, P260, P261, P264, P270, P271, P272, P273, P280, P281, P284, P285, P301+P310, P301+P330+P331, P302+P352, P303+P361+P353, P304+P340, P304+P341, P305+P351+P338, P308+P313, P310, P312, P314, P320, P321, P322, P330, P333+P313, P342+P311, P363, P391, P403+P233, P405, P501 | |
| NFPA 704 (fire diamond) | |
| Flash point | Non-flammable |
| Safety data sheet (SDS) | ICSC 1370 |
| Related compounds | |
Other anions | Sodium dichromate Sodium molybdate Sodium tungstate |
Other cations | Potassium chromate Calcium chromate Barium chromate |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Sodium chromate is the inorganic compound with the formula Na2CrO4. It exists as a yellow hygroscopic solid, which can form tetra-, hexa-, and decahydrates. It is an intermediate in the extraction of chromium from its ores.
Production and reactivity
[edit]It is obtained on a vast scale by roasting chromium ores in air in the presence of sodium carbonate:
- 2Cr2O3 + 4 Na2CO3 + 3 O2 → 4 Na2CrO4 + 4 CO2
This process converts the chromium into a water-extractable form, leaving behind iron oxides. Typically calcium carbonate is included in the mixture to improve oxygen access and to keep silicon and aluminium impurities in an insoluble form. The process temperature is typically around 1100 °C.[1] For lab and small scale preparations a mixture of chromite ore, sodium hydroxide and sodium nitrate reacting at lower temperatures may be used (even 350 C in the corresponding potassium chromate system).[2] Subsequent to its formation, the chromate salt is converted to sodium dichromate, the precursor to most chromium compounds and materials.[3] The industrial route to chromium(III) oxide involves reduction of sodium chromate with sulfur.
Acid-base behavior
[edit]It converts to sodium dichromate when treated with acids:
- 2 Na2CrO4 + 2HCl → Na2Cr2O7 + 2NaCl + H2O
Further acidification affords chromium trioxide:
- Na2CrO4 + H2SO4 → CrO3 + Na2SO4 + H2O
Uses
[edit]Aside from its central role in the production of chromium from its ores, sodium chromate is used as a corrosion inhibitor in the petroleum industry.[3] It is also a dyeing auxiliary in the textile industry.[3] It is a diagnostic pharmaceutical in determining red blood cell volume.[4]
In organic chemistry, sodium chromate is used as an oxidant, converting primary alcohols to carboxylic acids and secondary alcohols to ketones.[5] Sodium chromate is a strong oxidizer.
Safety
[edit]As with other Cr(VI) compounds, sodium chromate is carcinogenic.[6] The compound is also corrosive and exposure may produce severe eye damage or blindness.[7] Human exposure further encompasses impaired fertility, heritable genetic damage and harm to unborn children.
See also
[edit]References
[edit]- ^ IARC Monographs 49 Ch. 2 (PDF). ISBN 9789283212492.
- ^ Zhi Sun, Yi Zhang, Shi-Li Zheng, Yang Zhang (2009). "A new method of potassium chromate production from chromite and KOH-KNO3-H2O binary submolten salt system". AIChE Journal. 55 (10): 2646–2656. doi:10.1002/aic.11871.
{{cite journal}}: CS1 maint: multiple names: authors list (link) - ^ a b c Gerd Anger, Jost Halstenberg, Klaus Hochgeschwender, Christoph Scherhag, Ulrich Korallus, Herbert Knopf, Peter Schmidt, Manfred Ohlinger. "Chromium Compounds". Ullmann's Encyclopedia of Industrial Chemistry. Weinheim: Wiley-VCH. doi:10.1002/14356007.a07_067. ISBN 978-3527306732.
{{cite encyclopedia}}: CS1 maint: multiple names: authors list (link) - ^ Bracco Diagnostics Inc. "chromitope sodium (Sodium Chromate, Cr 51) injection, solution". DailyMed. Retrieved 2008-06-20.
- ^ Louis F. Fieser "Δ4-cholesten-3,6-dione" Org. Synth. 1955, 35, 36. doi:10.15227/orgsyn.035.0036
- ^ IARC (2012) [17-24 March 2009]. Volume 100C: Arsenic, Metals, Fibres, and Dusts (PDF). Lyon: International Agency for Research on Cancer. ISBN 978-92-832-0135-9. Archived from the original (PDF) on 2020-03-17. Retrieved 2020-01-05.
There is sufficient evidence in humans for the carcinogenicity of chromium (VI) compounds. Chromium (VI) compounds cause cancer of the lung. Also positive associations have been observed between exposure to Chromium (VI) compounds and cancer of the nose and nasal sinuses. There is sufficient evidence in experimental animals for the carcinogenicity of chromium (VI) compounds. Chromium (VI) compounds are carcinogenic to humans (Group 1).
- ^ "Potassium dichromate MSDS". JT Baker.
Further reading
[edit]- "Sodium chromate". inchem. Retrieved 2008-06-20.
- Record of Sodium chromate in the GESTIS Substance Database of the Institute for Occupational Safety and Health