Abstract
AbstractThe copolymerization of methyl acrylate (MA) and isobutylene (IB) in the presence of Lewis acids (EtAlCl2, Et2AlCl, Et3Al, AlCl3, and ZnCl2) at low Lewis acid/MA mole ratio was investigated. EtAlCl2 and Et2AlCl were found to initiate the spontaneous reaction. An alternating copolymer was produced in this reaction when an excess of IB in the initial monomer feed was used. The copolymerization in the presence of Et3Al, AlCl3, and ZnCl2 did not proceed spontaneously and was initiated by dibenzoyl peroxide (BPO). In this case MA‐rich copolymers are formed even in systems containing a large excess of IB in the monomer feed. The addition of BPO to systems containing ethylaluminium chlorides strongly diminishes the tendency towards alternating propagation. It was concluded that the mode of initiation has a significant influence on the copolymer composition. The alternating copolymerization by EtAlCl2 was studied in detail in order to determine the influence of the catalyst concentration, monomer feed ratio, reaction temperature and time on the monomer conversion, copolymer composition, molecular weight and tacticity.
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