Difference between revisions of "Chromium trioxide"
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==Preparation== | ==Preparation== | ||
− | Chromium trioxide can be prepared by reacting a Cr(VI) containing compound, such as [[sodium chromate]] | + | Chromium trioxide can be readily prepared by reacting a Cr(VI) containing compound, such as [[sodium|sodium chromate]]/[[sodium dichromate|dichromate]], or [[potassium|potassium chromate]]/[[potassium dichromate|dichromate]] with concentrated [[sulfuric acid]], albeit its purification is complicated. |
− | :H<sub>2</sub>SO<sub>4</sub> + Na<sub>2</sub>CrO<sub>4</sub> → CrO<sub>3</sub> + Na<sub>2</sub>SO<sub>4</sub> + H<sub>2</sub>O | + | : H<sub>2</sub>SO<sub>4</sub> + Na/K<sub>2</sub>CrO<sub>4</sub> → CrO<sub>3</sub> + Na/K<sub>2</sub>SO<sub>4</sub> + H<sub>2</sub>O |
− | :H<sub>2</sub>SO<sub>4</sub> + Na<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub> → 2 CrO<sub>3</sub> + Na<sub>2</sub>SO<sub>4</sub> + H<sub>2</sub>O | + | : H<sub>2</sub>SO<sub>4</sub> + Na/K<sub>2</sub>Cr<sub>2</sub>O<sub>7</sub> → 2 CrO<sub>3</sub> + Na/K<sub>2</sub>SO<sub>4</sub> + H<sub>2</sub>O |
− | The | + | Potassium dichromate is generally used, as it's cheap and more readily available. |
+ | |||
+ | Chromium trioxide can be obtained as such; in a beaker, 100 g of potassium dichromate is added. 200 ml of distilled water is added, and the solution is heated on a hotplate with a stirrer, until all the salt dissolves in the hot water. Then, 400 ml of conc. (98%) sulfuric acid is slowly added to the hot solution of dichromate, and this must be done carefully to prevent the solution from boiling, and all of this must be done outside or in a fume hood. After the H<sub>2</sub>SO<sub>4</sub> is added, the solution turns dark, and then another 200 ml of conc. sulfuric acid is added, while solution is cooled. This causes the chromium trioxide to precipitate out of the solution. Cooling the solution will cause more CrO<sub>3</sub> to precipitate, though the solution should not be cooled too much, as potassium bisulfate might precipitate out of the solution. The resulting thick suspension of chromium trioxide is filtered using a fritted glass funnel under vacuum. The crude filtrate still contains lots of sulfuric acid and leftover potassium sulfate salts, and needs washing. But because CrO<sub>3</sub> will react with water and most solvents, only conc. [[nitric acid]] (>65%) is suitable for washing this compound. The filtrate is washed using conc. nitric acid, and then it is dried using an oven and under vacuum. The final product may still contain traces of acids, which can be removed by further washing and vacuum drying.<ref>[https://www.youtube.com/watch?v=Hr-CsQDhgkc The Most Dangerous Chemical I've Ever Made.]</ref> | ||
==Projects== | ==Projects== |
Latest revision as of 21:18, 10 December 2024
Impure chromium trioxide
| |
Names | |
---|---|
IUPAC name
Chromium trioxide
| |
Other names
Chromic anhydride
Chromic acid anhydride Chromium(VI) oxide | |
Identifiers | |
Jmol-3D images | Image |
| |
Properties | |
CrO3 | |
Molar mass | 99.99 g/mol |
Appearance | Dark red solid |
Odor | Odorless |
Density | 2.7 g/cm3 (at 20 °C) |
Melting point | 197 °C (387 °F; 470 K) |
Boiling point | 250 °C (482 °F; 523 K) (decomposes) |
164.8 g/100 mL (0 °C) 169 g/100 mL (25 °C) 172.6 g/100 mL (40 °C) 198.1 g/100 mL (100 °C) | |
Solubility | Soluble in acetic acid, acetone, diethyl ether, nitric acid, sulfuric acid |
Vapor pressure | ~0 mmHg |
Thermochemistry | |
Std molar
entropy (S |
73.2 J/mol·K |
Std enthalpy of
formation (ΔfH |
−589.3 kJ/mol |
Hazards | |
Safety data sheet | ScienceLab |
Flash point | Non-flammable |
Lethal dose or concentration (LD, LC): | |
LD50 (Median dose)
|
80 mg/kg (rats, oral) |
Related compounds | |
Related compounds
|
Chromium(III) oxide |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
Infobox references | |
Chromium trioxide is an inorganic compound with the formula CrO3. It is a dark red/crimson solid, widely used in synthesis and industry. It is the acidic anhydride of chromic acid.
Contents
Properties
Chemical
Chromium trioxide decomposes above 197 °C, yielding chromium(III) oxide and liberating oxygen:
- 4 CrO3 → 2 Cr2O3 + 3 O2
It is used in organic synthesis as an oxidant, often as a solution in acetic acid, or acetone in the case of the Jones oxidation. In these oxidations, the Cr(VI) converts primary alcohols to the corresponding carboxylic acids and secondary alcohols to ketones.[1] The reactions are shown below:
Primary alcohols to carboxylic acids:
- 4 CrO3 + 3 RCH2OH + 12 H+ → 3 RCOOH + 4 Cr3+ + 9 H2O
Secondary alcohols to ketones:
- 2 CrO3 + 3 R2CHOH + 6 H+ → 3 R2C=O + 2 Cr3+ + 6 H2O
Dry chromium trioxide reacts violently with ethanol and other organic compounds, causing them to combust on contact.
Physical
Chromium trioxide is a dard red/crimson solid in its anhydrous form, and red-orange in aqueous solution. It is very soluble in water and soluble in some organic solvents, such as acetone or diethyl ether, as well as sulfuric acid.
Availability
Chromium trioxide is sold by various chemical suppliers, though due to its hazards it's not easy to get hold of.
Preparation
Chromium trioxide can be readily prepared by reacting a Cr(VI) containing compound, such as sodium chromate/dichromate, or potassium chromate/dichromate with concentrated sulfuric acid, albeit its purification is complicated.
- H2SO4 + Na/K2CrO4 → CrO3 + Na/K2SO4 + H2O
- H2SO4 + Na/K2Cr2O7 → 2 CrO3 + Na/K2SO4 + H2O
Potassium dichromate is generally used, as it's cheap and more readily available.
Chromium trioxide can be obtained as such; in a beaker, 100 g of potassium dichromate is added. 200 ml of distilled water is added, and the solution is heated on a hotplate with a stirrer, until all the salt dissolves in the hot water. Then, 400 ml of conc. (98%) sulfuric acid is slowly added to the hot solution of dichromate, and this must be done carefully to prevent the solution from boiling, and all of this must be done outside or in a fume hood. After the H2SO4 is added, the solution turns dark, and then another 200 ml of conc. sulfuric acid is added, while solution is cooled. This causes the chromium trioxide to precipitate out of the solution. Cooling the solution will cause more CrO3 to precipitate, though the solution should not be cooled too much, as potassium bisulfate might precipitate out of the solution. The resulting thick suspension of chromium trioxide is filtered using a fritted glass funnel under vacuum. The crude filtrate still contains lots of sulfuric acid and leftover potassium sulfate salts, and needs washing. But because CrO3 will react with water and most solvents, only conc. nitric acid (>65%) is suitable for washing this compound. The filtrate is washed using conc. nitric acid, and then it is dried using an oven and under vacuum. The final product may still contain traces of acids, which can be removed by further washing and vacuum drying.[2]
Projects
- Chrome plating
- Instantaneous ignition of alcohols
Handling
Safety
Chromium trioxide is a powerful oxidizer, highly toxic, corrosive, and carcinogenic. Avoid contact with alcohols.
Storage
Chromium trioxide should be kept in plastic or glass containers, with a proper label and a hazard symbol, in a dry place. If you're using glass, a good idea would be to keep the glass container inside a plastic container.
Since the compound ignites alcohols on contact, keep it away from any source of volatile solvents or products containing alcohols.
Disposal
A reducing agent, such as sodium metabisulfite, sodium sulfite or sodium thiosulfate can be used to turn CrO3 into the less toxic Cr(III) oxide. Glucose may also be used, albeit in a diluted solution. The neutralization must be done outside or in a fumehood, as the process will release Cr(VI) aerosoles, which are harmful and carcinogenic.
References
- ↑ Cotton, F. Albert; Wilkinson, Geoffrey; Murillo, Carlos A.; Bochmann, Manfred (1999), Advanced Inorganic Chemistry (6th ed.), New York: Wiley-Interscience
- ↑ The Most Dangerous Chemical I've Ever Made.
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