ABSTRACT
The study is related to an integrated process for the utilization of carbon dioxide to polymer blends via a copolymer bearing cyclic carbonate group. Poly(glycidyl methacrylate-co-acrylonitrile) [poly(PG MA-co-AN)] was converted to a poly[(2-oxo-1,3-dioxolane-4-yl) methyl methacrylate-co-acrylonitrile] [poly(DOMA-co-AN)] by the polymer reaction with carbon dioxide using quaternary ammonium salt as a catalyst. Among the quaternary salts tested, the one having a larger alkyl group and more nucleophilic counter anions, exhibited better catalytic activity in the addition of CO2 to poly(GMA-co-AN). In a semibatch reaction system, pseudo first-order rate equation agreed with the experimental results. The miscibility of poly(DOMA-co-AN) with styrene/acrylonitrile (SAN, 25 wt% of AN) copolymer or methyl methacrylate/ethyl acrylate (MMA-EA, 7 wt% of EA) copolymer has been investig ated both by differential scanning calorimetry (DSC) and visual inspection of the blends. Poly(DOMA-co-AN) formed clear films when blended with SAN or MMA-EA. DSC analysis also showed that poly(DOMA-co-AN) containing blends were miscible in the whole composition ranges. The glass transition temperatures (Tg) of the polymer blends closely matched the Fox equation.
ACKNOWLEDGMENTS
This work was supported by the Korea Science and Engineering Foundation (KOSEF 2000-2-30700-002-3) and Pusan National University Research Grant.