Uses
Additive to sealants, caulks, adhesives, and coatings.
Preparation
a-Methylstyrene is obtained from benzene and propylene by the following
route:
a-Methylstyrene is not readily polymerized by free radical initiators
but it is susceptible to cationic polymerization. Polymerization can be
effected, for example, in ethyl chloride at -130??C with aluminium chloride
but poly(a-methylstyrene) prepared in this manner is a clear brittle solid
which has little commercial application. Polymers with much lower molecular weight (300-600) obtained by using alkaline earth catalysts, however, are
viscous liquids and have found some use as plasticizers in surface coatings and adhesives.
Styrene-a-methylstyrene copolymers are marketed for extrusion and injection moulding. Compared to polystyrene, these copolymers have the advantage of higher softening points (104-106??C); they too are transparent and colourless.
