Thermal degradation of polymers is molecular deterioration as a result of overheating. At high temperatures the components of the long chain backbone of the polymer can begin to be broken (chain scission) and react with one another to change the properties of the polymer. Thermal degradation can present an upper limit to the service temperature of plastics as much as the possibility of mechanical property loss. Indeed unless correctly prevented, significant thermal degradation can occur at temperatures much lower than those at which mechanical failure is likely to occur. The chemical reactions involved in thermal degradation lead to physical and optical property changes relative to the initially specified properties. Thermal degradation generally involves changes to the molecular weight (and molecular weight distribution) of the polymer and typical property changes include reduced ductility and embrittlement, chalking, color changes, cracking, general reduction in most other desirable physical properties. Thermal breakdown products may include a complex mixture of compounds, including but not limited to carbon monoxide, ammonia, aliphatic amines, ketones, nitriles, and hydrogen cyanide, which may be flammable, toxic and/or irritating. The specific materials generated will vary depending on the additives and colorants used, specific temperature, time of exposure and other immediate environmental factors.
Most types of degradation follow a similar basic pattern. The conventional model for thermal degradation is that of an auto-oxidation process which involves the major steps of initiation, propagation, branching, and termination.
The initiation of thermal degradation involves the loss of a hydrogen atom from the polymer chain as a result of energy input from heat or light. This creates a highly reactive and unstable polymer ‘free radical’ (R•) and a hydrogen atom with an unpaired electron (H•).
The propagation of thermal degradation can involve a variety of reactions and one of these is where the free radical (R•) reacts with an oxygen (O2) molecule to form a peroxy radical (ROO•) which can then remove a hydrogen atom from another polymer chain to form a hydroperoxide (ROOH) and so regenerate the free radical (R•). The hydroperoxide can then split into two new free radicals, (RO•) + (•OH), which will continue to propagate the reaction to other polymer molecules. The process can therefore accelerate depending on how easy it is to remove the hydrogen from the polymer chain.