Common synthetic polymers that can be attacked include polypropylene and LDPE, where tertiary carbon bonds in their chain structures are the centres
of attack. Ultraviolet rays interact with these bonds to form free radicals, which then react further with oxygen in the atmosphere, producing
carbonyl groups in the main chain. The exposed surfaces of products may then discolour and crack, and in extreme cases, complete product
disintegration can occur.
Many organic chemicals are thermodynamically unstable in the presence of oxygen, however, their rate of spontaneous oxidation is slow at room
temperature. In the language of physical chemistry, such reactions are kinetically limited. This kinetic stability allows the accumulation of complex
environmental structures in the environment. Upon the absorption of light, triplet oxygen converts to singlet oxygen, a highly reactive form of the
gas, which effects spin-allowed oxidations. In the atmosphere, the organic compounds are degraded by hydroxyl radicals, which are produced from water
and ozone.[3]
Photochemical reactions are initiated by the absorption of a photon, typically in the wavelength range 290-700 nm (at the surface of the Earth). The
energy of an absorbed photon is transferred to electrons in the molecule and briefly changes their configuration (i.e., promotes the molecule from a
ground state to an excited state). The excited state represents what is essentially a new molecule. Often excited state molecules are not kinetically
stable in the presence of O2 or H2O and can spontaneously decompose (oxidize or hydrolyze). Sometimes molecules decompose to produce high energy,
unstable fragments that can react with other molecules around them. The two processes are collectively referred to as direct photolysis or indirect
photolysis |