Author/Authors :
FAWCETT، A. H. نويسنده , , T.MCNALLY، نويسنده , , MCNALLY، G. M. نويسنده ,
Abstract :
This paper summarizes the experimental results in a new class of polyolefm co- and terpolymers containing "reactive" p-methylstyrene ( p-MS) groups, which includes the materials from high Tm thermoplastics to low Tg elastomers. Due to the extraordinary copolymerization capability of metallocene catalysts with constrained ligand geometry, p-MS can be effectively copolymerized with (alpha)-olefins (i.e., ethylene, propylene, l-octene, etc.) to form co- and terpolymers having narrow molecular weight and composition distributions. Comparing with other relative styrenic comonomers, i.e., styrene, o-methylstyrene and m-methylstyrene, p-MS shows significantly higher reactivity in metallocene catalysis. In turn, the incorporated p-MS units in polyolefins are very versatile, which not only can be interconverted to various functional groups, such as -OH, -COOH, anhydride, silane and halides, but also can be conveniently transformed to "stable" anionic initiators for "living" anionic graft-from polymerization reactions. Many new functional polyolefin graft copolymers have been prepared, containing polyolefin backbone (PE, EP, EO, etc.) and functional polymer side chains, such as PMMA, PAN, PS, etc.
Keywords :
differential scanning calorimetry , fluorescence optical microscopy , bitumen , polymer , dynamic mechanical thermal analysis , Blend