The “comonomer effect” in ethylene/α‐olefin copolymerization using homogeneous and silica‐supported Cp2ZrCl2/MAO catalyst systems: Some insights from the kinetics of polymerization, active center studies, and polymerization temperature

Abstract

AbstractHomogeneous and silica‐supported Cp2ZrCl2/methylaluminoxane (MAO) catalyst systems have been used for the copolymerization of ethylene with 1‐butene, 1‐hexene, 4‐methylpentene‐1 (4‐MP‐1), and 1‐octene in order to compare the “comonomer effect” obtained with a homogeneous metallocene‐based catalyst system with that obtained using a heterogenized form of the same metallocene‐based catalyst system. The results obtained indicated that at 70 °C there was general rate depression with the homogeneous catalyst system whereas rate enhancement occurred in all copolymerizations carried out with the silica‐supported catalyst system. Rate enhancement was observed for both the homogeneous and the silica‐supported catalyst systems when ethylene/4‐MP‐1 copolymerization was carried out at 50 °C. Active center studies during ethylene/4‐MP‐1 copolymerization indicated that the rate depression during copolymerization using the homogeneous catalyst system at 70 °C was due to a reduction in the active center concentration. However, the increase in polymerization rate when the silica‐supported catalyst system was used at the same temperature resulted from an increase in the propagation rate coefficient. © 2007 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 46: 267–277, 2008