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Effect of 1‐Hexene Comonomer on Polyethylene Particle Growth and Kinetic Profiles
Author(s) -
van Grieken Rafael,
Carrero Alicia,
Suarez Inmaculada,
Paredes Beatriz
Publication year - 2007
Publication title -
macromolecular symposia
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.257
H-Index - 76
eISSN - 1521-3900
pISSN - 1022-1360
DOI - 10.1002/masy.200751329
Subject(s) - comonomer , 1 hexene , polymerization , polyethylene , hexene , polymer , polymer chemistry , ethylene , materials science , copolymer , chain transfer , catalysis , chemistry , radical polymerization , organic chemistry , composite material
Summary: The polymer growth and the microstructure of the final polymer are greatly affected by mass transfer, especially in the early stages of polymerization. In the present work, the catalytic system ( n BuCp) 2 ZrCl 2 /MAO immobilized over SiO 2 ‐Al 2 O 3 has been tested in ethylene‐1‐hexene copolymerizations using different amounts of comonomer. The catalytic activity shows a positive comonomer effect up to 1‐hexene concentration of 0.724 mol/L since larger amounts of 1‐hexene lead to a decrease in the activity. Copolymer properties analyzed by 13 C NMR, GPC, CRYSTAF and DSC point to the presence of important amorphous regions in the growing polymer chains as the 1‐hexene concentration increases. In order to study the incorporation of 1‐hexene during ethylene polymerization, several experiments were performed with 0.194 mol/L of 1‐hexene, 5 bar of ethylene pressure and different polymerization times. The incorporation of 1‐hexene decreases slightly at polymerization times above 20 minutes. From cross‐sectioned SEM images it can be concluded that the presence of 1‐hexene helps catalyst fragmentation which could be related with the filter effect proposed by Fink.