Polymer(Korea), Vol.23, No.4, 517-522, July, 1999
Rosin을 하뮤하는 광경화성 고분자의 합성과 특성
Synthesis and Properties of Phtocrosslinkable Polymers Containing Rosin Moiety
E-mail:
초록
트리메틸암모니늄브롬마이드를 촉매로 사용하여 abietic acid와 glycidylmethacrylate를 메틸에틸케톤 중에서 반응시켜 로진 moiety를 함유하는 아크릴단랑체 (AMR)을 합성하였다. AMRDMF 5-20 mol%의 감광성 단량체 cinnamoyloxymethylmaleimide (COMMI)와 라디칼 공중합하여 rosin moiety를 함유하는 몇 가지 광경화성 고분자를 합성하였다. UV 분광법과 원소분석으로 결정된 공중합체중의 COMMI함량은 4.6-21 mol%정도였다. 이들 고분자의 수평균 분자량은 20000-28000 정도였고 다분산지수는 1.8 정도였으며, 또한 이들 고분자의 유리전이온도는 140-175 ℃였고 초기 열분해온도는 250 ℃정도였다. 이들 고분자의 광경화반응은 UV분광법과 잔막 수율법으로 추적될 수 있었다.
Rosin moiety-containing monomer(AMR) was synthesized by reacting abietic acid and glycidylmethacrylate in methylethylketone using trimethylammonium bromide as a catalyst. Photocrosslinkable polymers containing rosin moiety were then prepared by radically copolymerizing AMR with cinnamoyloxymethylmaleimide(COMMI) as a photosensitive monomer. In these copolymerizations, the COMMI feed ratios of 5 to 20 mol% were used. The contents of COMMI units in the copolymers were determined to be 4.6 to 21 mol%. The number-average molecular weights of these polymers were in the range of 20000 to 28000 polydispersity indexes were about 1.8. The glass transition temperatures were ranged between 140 and 175 ℃, and the initial decomposition temperatures were about 250 ℃. In addition, the photocrosslinking reaction of these copolymers could be traced by the UV spectroscopy and the residual yield method.
- Stonecipher WD, Dimido AG, "Encyclopedia of Polymer Science and Technology," eds. by H.F. Mark and N.G. Gaylord, vol. 12, p. 139, Wiley & Interscience, New York (1970)
- Maiti M, Maiti S, J. Macromol. Sci.-Chem., 20, 109 (1983)
- Ray SS, Kundu AK, Maiti S, J. Macromol. Sci.-Chem., 23, 271 (1989)
- Kim JS, Choi HK, Polym.(Korea), 13(8), 692 (1989)
- Hoa JLTN, Pascault JP, My LT, Son CPN, Eur. Polym. J., 29, 491 (1993)
- Sowa JR, Marvel CS, J. Polym. Sci. C: Polym. Lett., 4, 431 (1966)
- Kim WS, Seo KH, Chang WS, Macromol. Rapid Commun., 17, 835 (1996)
- Palkin S, Harris TH, J. Am. Chem. Soc., 56, 1935 (1934)
- Liepins R, Marvel CS, J. Polym. Sci. A: Polym. Chem., 4, 2003 (1966)
- Kurihashi T, Kawashima M, Yamaguchi T, U.S. Patent, 5,644,010 (1997)
- Vanpaesschen G, Timmerman D, Makromol. Chem., 78, 112 (1964)
- Matsumoto A, Fukazawa A, Oiwa M, J. Appl. Polym. Sci., 28, 11 (1983)
- Nishikubo T, Yamada M, Iizawa Y, J. Polym. Sci. A: Polym. Chem., 21, 2025 (1983)
- Reiser A, Egerton PL, Macromolecules, 12, 670 (1979)
- Shindo Y, Sugimwa T, Horie K, Eur. Polym. J., 25, 1033 (1989)
- Torii T, Ushiki H, Horie K, Polym. J., 24, 1057 (1992)