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Influence of polymerization conditions on the copolymerization of styrene with ethylene using Me 2 Si(Me 4 Cp)( N ‐ tert ‐butyl)TiCl 2 /methylaluminoxane Ziegler‐Natta catalysts
Author(s) -
Sernetz Friedrich G.,
Mülhaupt Rolf,
Waymouth Robert M.
Publication year - 1996
Publication title -
macromolecular chemistry and physics
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.57
H-Index - 112
eISSN - 1521-3935
pISSN - 1022-1352
DOI - 10.1002/macp.1996.021970325
Subject(s) - copolymer , styrene , methylaluminoxane , polymer chemistry , ethylene , monomer , polymerization , differential scanning calorimetry , glass transition , materials science , activation energy , chemistry , catalysis , metallocene , polymer , organic chemistry , composite material , physics , thermodynamics
Styrene was copolymerized with ethylene using Me 2 Si(Me 4 Cp)( N‐tert ‐butyl)TiCl 2 /methylaluminoxane (Me = methyl, Cp = cyclopentadienyl) varying monomer concentration, styrene/ethylene molar ratio and polymerization temperature. Increasing styrene or decreasing ethylene concentration, respectively, in the monomer feed lowered both activity of the catalyst system and molecular weight of the copolymer. Only at low styrene content, a linear correlation of styrene concentration in the monomer feed and styrene incorporation in the copolymer was found. From copolymerizations at various temperatures the activation energy of the insertion step was calculated to be 56 kJ/mol. According to Fineman‐Ross plot, the copolymerization parameters are r E = 23,4 for ethylene and r S = 0,015 for styrene. Investigation of the thermal properties by means of differential scanning calorimetry and dynamic mechanical analysis revealed pronounced decrease of melting temperature and increase of glass transition temperature with increasing styrene content.