Preparation method and application of cycloolefin copolymer
A technology of cycloolefin copolymer and cycloolefin, which is applied in the field of preparation of cycloolefin copolymer, can solve the problems of inability to realize addition copolymerization, low polymerization activity, low catalytic activity, etc., and achieve high monomer conversion rate and high Catalytic activity, the effect of high catalytic activity
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Embodiment 1
[0061] This embodiment provides a kind of preparation method of cyclic olefin copolymer, concrete operation is as follows:
[0062] The polymerization reactor was pumped four times with high-purity nitrogen to discharge the air in the reactor, and then 3044g of toluene and cycloolefin monomer were added under the protection of nitrogen 160.2g (1.0mol), start stirring and heat up to 80°C, then add 99mg (0.5mmol) of triisobutylaluminum and 20.6mg (25μmol) of catalyst in sequence and organoboron compound B(C 6 f 5 ) 3 25.6 mg (50 μmol), and finally continue to feed ethylene gas to keep the ethylene pressure at 2.0 MPa, stop heating after 3 hours of reaction and cool to 25 °C. After the polymerization reaction was completed, it was terminated with acidified ethanol, and a white powdery solid was precipitated, which was washed with ethanol and suction-filtered to obtain cycloolefin copolymer A1, which was vacuum-dried at 70° C. for 8 hours.
Embodiment 2
[0064] This embodiment provides a kind of preparation method of cyclic olefin copolymer, concrete operation is as follows:
[0065] The polymerization reactor was pumped four times with high-purity nitrogen to discharge the air in the reactor, and then 1442g of toluene and cycloolefin monomer were added under the protection of nitrogen. 160.2g (1.0mol), start stirring and heat up to 80°C, then add 213mg (1.1mmol) of triisobutylaluminum and 44.4mg (53.8μmol) of catalyst in sequence and organoboron compound B(C 6 f 5 ) 3 55.1 mg (0.11 mmol), and finally continue to feed ethylene gas to keep the ethylene pressure at 0.5 MPa, stop heating after 10 hours of reaction and cool to 25 °C. After the polymerization reaction was completed, it was terminated with acidified ethanol, and a white powdery solid was precipitated, which was washed with ethanol and suction-filtered to obtain cycloolefin copolymer A2, which was vacuum-dried at 70° C. for 8 hours.
Embodiment 3
[0067] This embodiment provides a kind of preparation method of cyclic olefin copolymer, and the difference of specific operation and embodiment 1 is only not to add organoboron compound B (C 6 f 5 ) 3 , and other conditions remain the same. Cycloolefin copolymer A3 was obtained.
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