Premium
Poly(4‐vinylpyridine)‐supported cationic bis(cyclopentadienyl)zirconocene catalyst: Development of a new simple method to prepare polymer‐supported cationic zirconocene and its application to ethylene polymerization
Author(s) -
Musikabhumma Kittichote,
Uozumi Toshiya,
Sano Tsuneji,
Soga Kazuo
Publication year - 2000
Publication title -
macromolecular rapid communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 154
eISSN - 1521-3927
pISSN - 1022-1336
DOI - 10.1002/1521-3927(20000601)21:10<675::aid-marc675>3.0.co;2-i
Subject(s) - cationic polymerization , cyclopentadienyl complex , polymerization , polymer chemistry , polymer , catalysis , materials science , polyethylene , ethylene , crystallinity , solvent , copolymer , chemistry , organic chemistry , composite material
Bis(cyclopentadienyl)zirconocene dimethyl (Cp 2 ZrMe 2 ) combined with triphenylcarbenium tetrakis(pentafluorophenyl)borate ([Ph 3 C][B(C 6 F 5 ) 4 ]) was brought into contact with a suspension of 2% cross‐linked poly(4‐vinylpyridine) to give a new type of polymer‐supported cationic zirconocene catalyst. The resulting polymer‐supported catalyst system combined with Al( i‐ Bu 3 ) showed markedly high activity for ethylene polymerization in even a non‐polar solvent like hexane at 25–60°C and [Al]/[Zr] molar ratio 40–200. By the analysis of Zr content of the hexane solution, it was found that no Zr was detected in the solution, i. e. no leaching of the cationic catalyst into the hexane medium. The catalytic activity was found to increase with an increase of polymerization temperature and showed the highest at [Al]/[Zr] = 100. The molecular weight, crystalline melting temperature, crystallinity, and bulk density of polyethylene formed were higher than those of the polymer obtained from the homogeneous system.