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Video Microscopy for the Investigation of Gas Phase Copolymerization

✍ Scribed by Daniela Ferrari; Gerhard Fink


Publisher
John Wiley and Sons
Year
2005
Tongue
English
Weight
540 KB
Volume
290
Category
Article
ISSN
1438-7492

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✦ Synopsis


Abstract

Summary: Video microscopy as a tool for investigating olefin gas phase copolymerization is presented for the first time in this paper. The central theme of this work is the study of the comonomer effect shown by an unbridged metallocene catalyst supported on silica. By using video microscopy, it is possible to observe the increase in catalytic activity in terms of particle growth as well as monomer consumption. The observation that a more pronounced induction period in the particle growth profile is shown with increasing propylene concentration led us to investigate the copolymers obtained at different polymerization times using ^13^C NMR analysis and single particle energy dispersive X‐ray (EDX mapping). This allowed us to adapt the β€œpolymer growth and particle expansion model” to the copolymerization. Besides physical causes for the comonomer effect, we wanted to determine whether the catalyst structure plays an important role in the comonomer effect. To this end we investigated two metallocenes bearing the same long bridging unit but differing in the ligand bound to the zirconium center. One metallocene bears a cyclopentadienyl ring, while the other bears an indenyl group. From a close analysis of the ^13^C NMR, it is clear that both catalysts insert ethylene more easily then propylene, probably due to the long bridging unit that results in a narrower aperture angle of the ligand. In addition to this, the indenyl ligand does not allow the formation of propylene blocks even at high propylene concentration.

Snapshot of the polymer particles taken after 165 min of ethylene‐1‐butene copolymerization with catalyst 1.

imageSnapshot of the polymer particles taken after 165 min of ethylene‐1‐butene copolymerization with catalyst 1.


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The gas phase reaction of NzOs with water vapor was investigated in a 17.3-m' Teflon lined chamber. Temporal concentration profiles for ozone, total nitrogen oxides, and nitrogen dioxide were measured. Concentration profiles for N2OS and HNO, were calculated from a combination of measurements of nit