DONOR-MODIFIED AND ACCEPTOR-MODIFIED METALLOCENE-BASED HOMOGENEOUS ZIEGLER-NATTA CATALYSTS

The polymerization kinetics of propene polymerization using metallocene/methylaluminoxane (MAO) homogeneous catalysts have been investigated to explore the role of donor/acceptor interactions and to enhance the catalyst productivities. In the case of the non-stereospecific Cp2ZrCl/MAO model system it has been demonstrated that, in addition to the wen known irreversible deactivation, reversible deactivations, which are second order relative to the zirconium active site concentration, account for the decay of the polymerization rate. While MAO injection during polymerization enhances the polymerization rate, zirconocene addition deactivates the catalyst which can be reactivated by injecting additional MAO. A sequence of dynamic equilibria involving the formation of active cationic metallocene intermediates as well as inactive zirgonocene species, e.g., zirconocene dimers, is proposed. Lewis base and Lewis acid additives have been added as probes to examine the role of such equilibria in the case of metallocene-based catalyst systems such as MAO-activated Cp2ZrCl2, racemic ethylenebisindenyl zirconium dichloride (EBlZrCl2), and racemic ethylenebis (4,5,6,7-tetrahydroindenyl) zirconium dichloride (EBTHlZrCl2). While the conventional donors such as 2,6-ditert.butyl-4-methylphenol (BHT) and 2,2,6,6-tetramethylpiperidine (TMP) reduce catalyst productivities, even at very low donor/Al molar ratios, increasing propene concentration and addition of trimethylboroxine (TMB) substantially enhance catalyst productivities and affect molecular weights of the polypropylene produced with metallocene/MAO catalysts.