Dynamic balance of ozone formation and destruction
- Stratospheric ozone concentrations have remained relatively constant for thousands of years because ozone formation and ozone destruction occur at the same rate.
- UV radiation naturally splits oxygen molecules (O₂) into individual oxygen atoms (O), which then recombine with O₂ to form ozone (O₃).
- When an O₃ molecule absorbs UV radiation, it breaks apart into O₂ + O, meaning the destruction process is also natural.
- The steady state equilibrium exists because ozone destroyed = ozone produced, maintaining a stable ozone concentration under natural conditions.
- Although the ozone layer fluctuates seasonally and geographically, long-term concentrations remain stable under natural, pre-industrial conditions.
Ozone Formation and Destruction
Formation of Ozone
- Ozone (O₃) is formed when ultraviolet (UV-C) radiation from the Sun breaks apart molecular oxygen (O₂) in the stratosphere.
- The freed oxygen atoms (O) then react with other O₂ molecules to form ozone (O₃).
This process predominantly occurs in the stratosphere, between 15-35 km above Earth’s surface.
Destruction of Ozone
- Ozone is naturally destroyed when it absorbs UV radiation, splitting back into an oxygen molecule (O₂) and a free oxygen atom (O).
- The free oxygen atom can then recombine with another ozone molecule, breaking it down into more oxygen molecules.
- This cycle continuously occurs, maintaining an equilibrium concentration of ozone in the stratosphere.
- This balance is not static.
- It is a dynamic equilibrium, meaning the processes of formation and destruction are continuously occurring.
Ozone-Depleting Substances (ODSs) and Their Impact on the Ozone Layer
Ozone-depleting substances (ODSs)
Ozone-depleting substances (ODSs) are chemicals that accelerate ozone destruction beyond natural levels.
- Ozone-depleting substances (ODSs) accelerate the destruction of ozone molecules, disrupting the natural equilibrium between ozone formation and breakdown in the stratosphere.
- This imbalance leads to ozone depletion, especially over polar regions like Antarctica.
- They include chlorofluorocarbons (CFCs), halons, hydrochlorofluorocarbons (HCFCs), carbon tetrachloride and methyl bromide.
- These substances were extensively used because they were non-toxic, non-reactive and excellent refrigerants, which made them popular in:
- Aerosols
- Refrigeration and air-conditioning
- Gas-blown insulating foams
- Fire-extinguishing systems
- Agricultural fumigants
Key ODSs and Their Effects
- Chlorofluorocarbons (CFCs): Used in refrigeration, air conditioning, and aerosol propellants.
- Halons: Found in fire extinguishers.
- Hydrochlorofluorocarbons (HCFCs): Transitional substitutes for CFCs but still have ozone-depleting potential.
- Methyl bromide: Used as a pesticide but phased out due to its ozone-depleting effects.
How ODSs disrupt ozone equilibrium
- ODS molecules slowly migrate to the stratosphere because they are chemically stable in the troposphere.
- In the stratosphere, exposure to strong UV radiation breaks ODS molecules apart.
- This releases halogen radicals (especially chlorine and bromine) that trigger chain reactions destroying ozone molecules faster than they are formed.
- One chlorine atom can destroy up to 100,000 ozone molecules before being removed, which massively disrupts equilibrium.
The rapid increase in atmospheric CFCs during the 1970s–1990s correlated strongly with a sharp decline in Dobson Unit values over Antarctica, leading to the world’s first recognized “ozone hole.”


