Ethylene Copolymerization with Linear and End-Cyclized Olefins via a Metallocene Catalyst: Polymerization Behavior and Thermal Properties of Copolymers

Abstract

Olefin solution polymerization can be used to obtain high-performance polyolefin materials that cannot be obtained via other polymerization processes. Polyolefin elastomers (POE) are a typical example. Due to cost, only a few linear α-olefins (e.g., 1-butene, 1-hexene, and 1-octene) are used as comonomers in solution polymerization in industry. However, α-olefin comonomers with other structures may have different effects on polymerization in comparison with common linear ones. Moreover, the properties of the corresponding materials may differ significantly. In this work, copolymers of ethylene with linear and end-cyclized α-olefins are synthesized using a metallocene catalyst. The copolymerization of ethylene with linear α-olefins results in a higher turn-over frequency (TOF) and lower incorporation than copolymerization with end-cyclized α-olefins, which may indicate that end-cyclized α-olefins have a higher coordination probability and lower insertion rate. In this reaction, the comonomer is distributed randomly in the polymer chain and efficiently destroys crystallization. End-cyclized α-olefins exhibit a much stronger crystallization destructive capacity (CDC) in the copolymer than linear α-olefins, possibly because linear α-olefins act mainly in the radial direction of the main chain of the polymer, while end-cyclized α-olefins act mainly in the axial direction of the main chain.

Keywords

• Metallocene catalyst
• Ethylene copolymerization
• Comonomer distribution
• Crystallization destructive capacity