Cyclic olefin-based copolymers and methods for their preparation
A technology of cyclic olefin and binary copolymer, applied in the field of cyclic olefin-based copolymer and preparation thereof, can solve the problems of operability, insufficient heat resistance, etc.
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Embodiment 1
[0067] 20 g of the polymer obtained in Comparative Example 1 was dissolved in 60 g of dichloromethane. While stirring, the temperature was lowered to 0° C., and 8.6 g of mCPBA (m-chloroperoxybenzoic acid) was slowly added dropwise. After stirring for 1 hour, the temperature was raised to room temperature, followed by reaction for 5 hours. After the reaction, the reaction mixture was filtered, and the obtained reaction solution was poured into excess methanol to obtain a white solid precipitate. The precipitate was filtered with a glass funnel, and dried in a vacuum oven at 30°C for 24 hours to obtain a copolymer having an epoxy conversion of 30% and a repeating unit of Chemical Formula 1:a repeating unit of Chemical Formula 2 in a molar ratio of 3:7 (Mw = 5600 g / mol, PDI = 1.95, yield 80%).
Embodiment 2
[0069] In the same manner as in Example 1, the epoxy conversion rate was 60% and the repeating unit of chemical formula 1: the molar ratio of the repeating unit of chemical formula 2 was a copolymer of 6:4 (Mw=5700g / mol, PDI=1.97, Yield 82%), except that the content of mCPBA (m-chloroperoxybenzoic acid) was changed from 8.6 g to 17.2 g.
Embodiment 3
[0079] In the same manner as in Example 1, the epoxy conversion rate was 30% and the repeating unit of chemical formula 1: the molar ratio of the repeating unit of chemical formula 2 was a copolymer (Mw=7800g / mol, PDI=2.08, Yield 80%), except that the polymer of Comparative Example 1 was changed to the polymer of Comparative Example 5.
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