Macromolecular Chemistry and Physics · 2000 · 16 citations · 0 references
Natural SciencesChemical EngineeringChemistryOrganic ChemistryPolymer ChemistryPolymer MaterialsFree-radical PolymerizationPolymer CharacterizationPolymer ProcessingPolymer SynthesisPolymerization ChemistryPolymerization ProcessesCopolymer Composition AnalysisCopolymerizationCopolymerization KineticsElemental Abundance AnalysisMonomer Reactivity RatiosPolymer-monomer RatioTemperature Dependence Of Polymerization
Free-radical copolymerizations of ethene (E) with methacrylic acid (MAA) and of E with acrylic acid (AA) were carried out in a continuously operated tank reactor at 2000 bar and temperatures up to 280°C. The (M)AA content of the polymer, F(M)AA, that may be reached by polymerization in homogeneous phase, e. g., at 260°C, is below 10 mol-% and the associated (M)AA content of the monomer mixture is below 1 mol-%. Under such conditions, the ethene and the comonomer reactivity ratios, rE and r(M)AA, respectively, can not be simultaneously derived by fitting the measured F(M)AA and f(M)AA data according to the classical procedure. With r(M)AA, however, being available from a preceding 13C NMR study1), rE may be calculated from each pair of experimental F(M)AA and f(M)AA values. F(M)AA values are determined by means of elemental analysis of carbon and oxygen with consistency checks of copolymer composition being performed via FT-IR spectroscopy on polymeric films. f(M)AA is deduced from the measured monomer feed fluxes and from the amount and composition of the copolymer produced within given intervals of stationary polymerization. The rE data for the E/MAA and E/AA systems are presented and discussed. At identical polymerization pressure and temperature, the measured rE values of both systems agree within about ± 10%. The rE values, in addition, are very close to the ethene reactivity ratios that were recently measured for several E/(meth)acrylate copolymerizations. Arguments for this family-type behavior of rE are discussed.