Ammonium dichromate

[5] It is also used as a mordant for dyeing pigments, in manufacturing of alizarin, chrome alum, leather tanning and oil purification.

[6] The volcano demonstration involves igniting a pile of the salt, which initiates the following exothermic conversion:- [8] Like ammonium nitrate, it is thermodynamically unstable.

[9][10] Its decomposition reaction proceeds to completion once initiated, producing voluminous dark green powdered chromium(III) oxide.

The characteristic darkening of (NH4)2Cr2O7 crystals as a consequence of the onset of decomposition can be ascribed to the dissociative loss of ammonia accompanied by progressive anion condensation to Cr3O2−10, Cr4O2−13, etc., ultimately yielding CrO3.

Ammonium dichromate, in the presence of Mg(HSO4)2 and wet SiO2 can act as a very efficient reagent for the oxidative coupling of thiols under solvent free conditions.

[9] In 1986, two workers were killed and 14 others injured at Diamond Shamrock Chemicals in Ashtabula, Ohio, when 2,000 lb (910 kg) of ammonium dichromate exploded as it was being dried in a heater.

NFPA 704 four-colored diamond Health 4: Very short exposure could cause death or major residual injury. E.g. VX gas Flammability 2: Must be moderately heated or exposed to relatively high ambient temperature before ignition can occur. Flash point between 38 and 93 °C (100 and 200 °F). E.g. diesel fuel Instability 3: Capable of detonation or explosive decomposition but requires a strong initiating source, must be heated under confinement before initiation, reacts explosively with water, or will detonate if severely shocked. E.g. hydrogen peroxide Special hazard OX: Oxidizer. E.g. potassium perchlorate
A few drops of ethanol are added to a small pile of ammonium dichromate ((NH 4 ) 2 Cr 2 O 7 ) and ignited. Sparks are emitted and an ash-like product is formed. The phenomenon resembles the eruption of a volcano. The reaction starts at 180 °С, becoming self-sustaining at approximately 225 °С. [ 7 ]
Ammonium dichromate decomposition