A kind of cyclic olefin copolymer and preparation method thereof
A cyclic olefin copolymer and cyclic olefin technology, applied in the field of cyclic olefin copolymer, can solve the problems of harsh equipment and reaction conditions, etc.
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[0036]The present invention also provides a preparation method of the above-mentioned cycloolefin copolymer, comprising the following steps: dissolving the above-mentioned comonomer and metathesis polymerization catalyst in a solvent and dispersing them uniformly; removing the solvent under reduced pressure, and injecting the obtained liquid composition into a molding mold Inside; temperature rise for copolymerization reaction.
[0037] In the preparation method according to the present invention, the dissolving, dispersing and depressurizing steps have no limitation on the temperature of the system, as long as the comonomer and the metathesis polymerization catalyst are uniformly dispersed in the solvent, and the solvent can be discharged out of the system smoothly That's it. In order to prevent the comonomer and the metathesis polymerization catalyst from starting to react before entering the molding die, resulting in an increase in the viscosity of the system, in the steps ...
Embodiment 1
[0044] This example is used to illustrate the cycloolefin copolymer of the present invention and its preparation method.
[0045] Get the dicyclopentadiene of 100 molar parts, 0.04 molar parts dichloro (o-isopropoxyphenylmethylene) (tricyclohexylphosphine) ruthenium (II), 1 molar part of bismaleyl shown in formula I imine (where R 1 and R 2 Both are hydrogen atoms) and mixed evenly, placed in a 50mL single-necked flask, added 5mL of purified n-pentane, stirred at 30°C to dissolve, and vacuumed to remove the solvent in the system. When the reactant becomes a viscous liquid, it is poured into a mold preheated at 30° C., and the temperature is gradually raised to carry out ring-opening polymerization to obtain a copolymer P1. Heating temperature and time: 70°C (4h) + 130°C (3h) + 160°C (4h) + 185°C (3h) + 200°C (3h).
Embodiment 2
[0047] This example is used to illustrate the cycloolefin copolymer of the present invention and its preparation method.
[0048] Take 40 molar parts of norbornene, 60 molar parts of methyldicyclopentadiene, 0.2 molar parts of [1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene] Dichloro(benzylidene) (tricyclohexylphosphine) ruthenium, bismaleimide (wherein R shown in 15 mole parts formula II 1 is methyl, R 2 is a hydrogen atom), mix well, place in a 50mL single-necked flask, add 2mL of purified CH 2 Cl 2 , Stir at -20°C to dissolve it, and remove the solvent in the system by vacuuming. When the reactant becomes a viscous liquid, it is poured into a preheated mold at 30°C and the temperature is gradually raised to carry out ring-opening polymerization to obtain the copolymer P2. Heating temperature and time: 40°C (3h) + 100°C (4h) + 150°C (2h) + 165°C (4h) + 190°C (4h).
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