Potassium dichromate

Potassium dichromate is usually prepared by the reaction of potassium chloride on sodium dichromate. Alternatively, it can be also obtained from potassium chromate by roasting chromite ore with potassium hydroxide. It is soluble in water and in the dissolution process it ionizes:

K₂Cr₂O₇ → 2 K⁺ + Cr
₂O²⁻
₇

Cr
₂O²⁻
₇ + H₂O ⇌ 2 CrO²⁻
₄ + 2 H⁺

Potassium dichromate is an oxidising agent in organic chemistry, and is milder than potassium permanganate. It is used to oxidize alcohols. It converts primary alcohols into aldehydes and, under more forcing conditions, into carboxylic acids. In contrast, potassium permanganate tends to give carboxylic acids as the sole products. Secondary alcohols are converted into ketones. For example, menthone may be prepared by oxidation of menthol with acidified dichromate.[7] Tertiary alcohols cannot be oxidized.

In an aqueous solution the color change exhibited can be used to test for distinguishing aldehydes from ketones. Aldehydes reduce dichromate from the +6 to the +3 oxidation state, changing color from orange to green. This color change arises because the aldehyde can be oxidized to the corresponding carboxylic acid. A ketone will show no such change because it cannot be oxidized further, and so the solution will remain orange.

When heated strongly, it decomposes with the evolution of oxygen.

4 K₂Cr₂O₇ → 4 K₂CrO₄ + 2 Cr₂O₃ + 3 O₂

When an alkali is added to an orange-red solution containing dichromate ions, a yellow solution is obtained due to the formation of chromate ions (CrO2−4). For example, potassium chromate is produced industrially using potash:

K₂Cr₂O₇ + K₂CO₃ → 2 K₂CrO₄ + CO₂

The reaction is reversible.

Treatment with cold sulfuric acid gives red crystals of chromic anhydride (chromium trioxide, CrO₃):

K₂Cr₂O₇ + 2 H₂SO₄ → 2 CrO₃ + 2 KHSO₄ + H₂O

On heating with concentrated acid, oxygen is evolved:

2 K₂Cr₂O₇ + 8 H₂SO₄ → 2 K₂SO₄ + 2 Cr₂(SO₄)₃ + 8 H₂O + 3 O₂

Like other chromium(VI) compounds (chromium trioxide, sodium dichromate), potassium dichromate has been used to prepare "chromic acid" for cleaning glassware and etching materials. Because of safety concerns associated with hexavalent chromium, this practice has been largely discontinued.

It is used as an ingredient in cement in which it retards the setting of the mixture and improves its density and texture. This usage commonly causes contact dermatitis in construction workers.[9]

In 1839, Mungo Ponton discovered that paper treated with a solution of potassium dichromate was visibly tanned by exposure to sunlight, the discoloration remaining after the potassium dichromate had been rinsed out. In 1852, Henry Fox Talbot discovered that exposure to ultraviolet light in the presence of potassium dichromate hardened organic colloids such as gelatin and gum arabic, making them less soluble.

These discoveries soon led to the carbon print, gum bichromate, and other photographic printing processes based on differential hardening. Typically, after exposure, the unhardened portion was rinsed away with warm water, leaving a thin relief that either contained a pigment included during manufacture or was subsequently stained with a dye. Some processes depended on the hardening only, in combination with the differential absorption of certain dyes by the hardened or unhardened areas. Because some of these processes allowed the use of highly stable dyes and pigments, such as carbon black, prints with an extremely high degree of archival permanence and resistance to fading from prolonged exposure to light could be produced.

Dichromated colloids were also used as photoresists in various industrial applications, most widely in the creation of metal printing plates for use in photomechanical printing processes.

Chromium intensification or Photochromos uses potassium dichromate together with equal parts of concentrated hydrochloric acid diluted down to approximately 10% v/v to treat weak and thin negatives of black and white photograph roll. This solution reconverts the elemental silver particles in the film to silver chloride. After thorough washing and exposure to actinic light, the film can be redeveloped to its end-point yielding a stronger negative which is able to produce a more satisfactory print.

A potassium dichromate solution in sulfuric acid can be used to produce a reversal negative (that is, a positive transparency from a negative film). This is effected by developing a black and white film but allowing the development to proceed more or less to the end point. The development is then stopped by copious washing and the film then treated in the acid dichromate solution. This converts the silver metal to silver sulfate, a compound that is insensitive to light. After thorough washing and exposure to actinic light, the film is developed again allowing the previously unexposed silver halide to be reduced to silver metal. The results obtained can be unpredictable, but sometimes excellent results are obtained producing images that would otherwise be unobtainable. This process can be coupled with solarisation so that the end product resembles a negative and is suitable for printing in the normal way.

Cr(VI) compounds have the property of tanning animal proteins when exposed to strong light. This quality is used in photographic screen-printing.

In screen-printing a fine screen of bolting silk or similar material is stretched taut onto a frame similar to the way canvas is prepared before painting. A colloid sensitized with a dichromate is applied evenly to the taut screen. Once the dichromate mixture is dry, a full-size photographic positive is attached securely onto the surface of the screen, and the whole assembly exposed to strong light – times vary from 3 minutes to a half an hour in bright sunlight – hardening the exposed colloid. When the positive is removed, the unexposed mixture on the screen can be washed off with warm water, leaving the hardened mixture intact, acting as a precise mask of the desired pattern, which can then be printed with the usual screen-printing process.

Because it is non-hygroscopic, potassium dichromate is a common reagent in classical "wet tests" in analytical chemistry.

Acidified solution of potassium dichromate

The concentration of ethanol in a sample can be determined by back titration with acidified potassium dichromate. Reacting the sample with an excess of potassium dichromate, all ethanol is oxidized to acetic acid:

CH₃CH₂OH + 2[O] → CH₃COOH + H₂O

Full reaction of converting ethanol to acetic acid:

3 C₂H₅OH + 2 K₂Cr₂O₇ + 8 H₂SO₄ → 3 CH₃COOH + 2 Cr₂(SO₄)₃ + 2 K₂SO₄ + 11 H₂O

The excess dichromate is determined by titration against sodium thiosulfate. Adding the amount of excess dichromate from the initial amount, gives the amount of ethanol present. Accuracy can be improved by calibrating the dichromate solution against a blank.

One major application for this reaction is in old police breathalyzer tests. When alcohol vapor makes contact with the orange dichromate-coated crystals, the color changes from Cr(VI) orange to Cr(III) green. The degree of the color change is directly related to the level of alcohol in the suspect's breath.

When dissolved in an approximately 35% nitric acid solution it is called Schwerter's solution and is used to test for the presence of various metals, notably for determination of silver purity. Pure silver will turn the solution bright red, sterling silver will turn it dark red, low grade coin silver (0.800 fine) will turn brown (largely due to the presence of copper which turns the solution brown) and even green for 0.500 silver. Brass turns dark brown, copper turns brown, lead and tin both turn yellow while gold and palladium do not change.

Potassium dichromate paper can be used to test for sulfur dioxide, as it turns distinctively from orange to green. This is typical of all redox reactions where hexavalent chromium is reduced to trivalent chromium. Therefore, it is not a conclusive test for sulfur dioxide. The final product formed is Cr₂(SO₄)₃.

${\displaystyle {\ce {SO2 + K2Cr2O7 + 3H2SO4 -> K2SO4 + Cr2(SO4)3 + 3H2O}}}$

Potassium dichromate is used to stain certain types of wood by darkening the tannins in the wood. It produces deep, rich browns that cannot be achieved with modern color dyes. It is a particularly effective treatment on mahogany.[10]