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Styrene is an organic compound with the chemical formula C 6 H 5 CH=CH 2. Its structure consists of a vinyl group as substituent on benzene. Styrene is a colorless, oily liquid, although aged samples can appear yellowish. The compound evaporates easily and has a sweet smell, although high concentrations have a less pleasant odor.
The styrene monomer (from which polystyrene is made) is a cancer suspect agent. [109] Styrene is "generally found in such low levels in consumer products that risks aren't substantial". [110] Polystyrene which is used for food contact may not contain more than 1% (0.5% for fatty foods) of styrene by weight. [111]
Styrene, for example, is distilled at temperatures above 100 °C whereupon it undergoes thermal polymerisation at a rate of ~2% per hour. [1] This polymerisation is undesirable, as it can foul the fractionating tower ; it is also typically exothermic , which can lead to a runaway reaction and potential explosion if left unchecked.
Styrene-butadiene is a commodity material which competes with natural rubber. The elastomer is used widely in pneumatic tires. This application mainly calls for E-SBR, although S-SBR is growing in popularity. Other uses include shoe heels and soles, gaskets, and even chewing gum. [3]
Styrene monomer (SM) is an intermediate product. It is a colorless liquid that polymerizes easily. Polystyrene (PS) is a thermoplastic resin that is used in many applications, such as disposable packaging, electronic devices, large appliances (for example in refrigeration liners) and household goods.
On the other hand, the use of milder conditions such as acetyl sulfate leads to incomplete sulfonation. Recently, the atom transfer radical polymerization (ATRP) of protected styrene sulfonates has been reported, [12] [13] leading to well defined linear polymers, as well as more complicated molecular architectures. [14]
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