Group IX of the periodic table contains the transition metal cobalt, which is vital in many applications due to its special chemical and physical characteristics. Cobalt is very useful in the creation of magnetic and heat-resistant alloys because of its physical properties, which are comparable to those of iron and nickel. Beyond its industrial uses, cobalt plays a crucial role in biological processes, supporting the proper functioning of the nervous system and DNA production in many living organisms, including humans.
Cobalt (Co) is a transition metal on the periodic table, with an atomic number of 27 and an atomic mass of 58.933195. It was first discovered in 1735 by George Brandt in Stockholm, Sweden. Cobalt has many applications today, including in magnets, paint pigments, glass, and even cancer therapy. The name “cobalt” comes from the German word kobold, meaning "goblin" or "evil spirit," a term used by miners due to the metal's challenging extraction and the health hazards associated with it.
The stable form of cobalt can be produced in supernovae through the r-process, making up about 0.0029% of the Earth’s crust. Pure, or native, cobalt metal is not typically found on Earth due to the abundance of chlorine in seawater and oxygen in the atmosphere, which prevents its formation in a natural metallic form.
While pure cobalt metal is rarely found on Earth, except in meteoric iron, cobalt compounds are more widely distributed. Though cobalt is moderately abundant, its compounds are found in trace amounts in many soils, rocks, animals, and plants.
Cobalt is a moderately reactive element. It reacts with oxygen in the air, though it does not ignite or burn unless in powdered form. Cobalt also reacts with most acids to produce hydrogen gas but is stable in water at room temperature.
In aqueous solutions, cobalt forms the pink hexaaquacobalt(II) ion, [Co(H2O)6]2+. This ion, which changes from blue (dry form) to pink (hydrated form), is commonly used in cobalt (II) chloride humidity indicators.
When hydroxide ions are introduced, they deprotonate the water ligands attached to the cobalt ion, forming a neutral, water-insoluble complex that precipitates:
[Co(H2O)6]2++ 2OH−→ [Co(H2O)4(OH)2] + 2H2O
Ammonia acts as both a ligand and a base. Adding a small amount of ammonia forms the same neutral complex as with hydroxide:
[Co(H2O)6]2++2NH3 → [Co(H2O)4(OH)2] + 2NH4+
When excess ammonia is added, it fully replaces water as a ligand, forming hexaamminecobalt(II) ions:
[Co(H2O)6]2++ 6NH3→[Co(NH3)6]2++ 6H2O
The hexaamminecobalt(II) complex readily oxidises to cobalt(III) upon exposure to air, forming a deep red-brown solution due to a mix of cobalt(III) complexes.
Adding hydrogen peroxide after ammonia accelerates oxidation, turning the solution dark red-brown:
2[Co(NH3)6]2++H2O2 → 2[Co(NH3)6]3++ 2OH−
With sodium hydroxide, cobalt(II) hydroxide precipitates, and hydrogen peroxide addition produces oxygen bubbles and a chocolate-brown precipitate of cobalt(III).
Hexaaquacobalt(II) ions react with carbonate ions to form a basic cobalt carbonate precipitate:
Co2++CO32−→CoCO3
This precipitate is often a basic carbonate with a general formula.
When concentrated hydrochloric acid is added to a hexaaquacobalt(II) solution, it turns blue as chloride ions replace the water ligands:
[Co(H2O)6]2++ 4Cl− ⇌ [CoCl4]2−+ 6H2O
This reaction is reversible and highlights the colour change associated with ligand exchange.
Cobalt is a metal with a wide range of applications across various industries. Its diverse uses support sectors such as clean energy, transportation, healthcare, and petrochemicals. Some of the key applications of cobalt include:
(Session 2025 - 26)