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아크릴/우레아 가교 폴리머의 하이솔리드 도료에의 적용

Acrylic/Urea Crosslinked Polymers for High-Solid Coatings Applications

  • 정동진 (명지대학교 공과대학 화학공학과) ;
  • 박형진 (명지대학교 공과대학 화학공학과) ;
  • 김성래 (명지대학교 공과대학 화학공학과) ;
  • 함현식 (명지대학교 공과대학 화학공학과) ;
  • 박홍수 (명지대학교 공과대학 화학공학과) ;
  • 김성길 (삼화페인트공업(주))
  • 발행 : 2003.03.31

초록

Environmental friendly acrylics/urea high-solid paints (BEHCU) were prepared through the curing reaction of acrylics resin(BEHC) containing 70wt% of solids content and butylated urea curing agent. BEHC was synthesized by addition copolymerization of caprolactone acrylate(CLA), 2-hydroxypropyl methacrylate(2-HPMA), ethyl methacrylate, and n-butyl acrylate. The addition polymerization of these monomers, especially including flexible CLA monomer and 2-HPMA monomer with OH funtional group, under appropriate reaction conditions resulted in polymers with controlled glass transition temperature($T_g$) and crosslinking density. The molecular weight($M_w$) of these polymers(BEHCs) was 2940${\sim}$3240 and polydispersity ($M_w/M_n$) was in the range of 1.61${\sim}$1.72. The viscosity and the molecular weight of these acrylic resins increased with increasing $T_g$. The coated films were prepared using curing reaction between BEHC resin and butylated urea curing agent at 100$^{\circ}C$ for 30 minutes. Our experimental resulted showed that enhancement of the coating properties such as adhesion, flexibility, impact resistance, water resistance, and abrasion resistance could be expected through introducing CLA component in acrylic resin for the high-solid content acrylics/urea coatings.

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참고문헌

  1. E. Denise and F. Fiori, Progress in Organic Coatings, 32(1-4), 65 (1997) https://doi.org/10.1016/S0300-9440(97)00076-3
  2. V. R. Kamath and J. D. Sargent, Jr., J. Coat. Technol., 59(746), 51 (1987)
  3. A. T. Chen, L. E. Katz, R. T. Wojcik, and J. M. O'Connor, 'Novel Water-Borne Polyurethane Coatings', Waterborne, High-Solids, and Powder Coatings Symposium, Feb. 14-16, New Orleans (1996)
  4. J. J. Gummeson, J. Coat. Technol., 62(785), 43 (1990)
  5. C. M. Neag and R. B. Prime, J. Coat. Technol., 63(797), 37 (1991)
  6. T. Morimoto and S. Nakano, J. Coat. Technol., 66(833), 75 (1994)
  7. R. Buter, J. Coat. Technol., 59(749), 37 (1987)
  8. H. S. Hahm and H. S. Park, J. Kor. Soc. Text. Eng. Chemists, 26, 208 (1989)
  9. G. Haacke, J. S. Brinen, and P. J. Larkin, J. Coat. Technol., 67(843), 29 (1995)
  10. B. J. Exsted and M. W. Urban, J. Appl. Polym. sci, 47, 2019 (1993) https://doi.org/10.1002/app.1993.070471113
  11. J. D. Nordstrom and A. H. Dervan, 'Blocked Isocyanate Crosslinkers for Automotive Topcoats' ,16th Water-Borne & Higher-Solids, and Powder Coatings Symposium, 16, 2 (1989)
  12. C. A. Zezza and K. D. Talmo, J. Coat. Technol., 68(856), 49 (1996)
  13. L. J. Boggs, M. Rivers, and S. G. Bike, J. Coat. Technol., 68(855), 63 (1996)
  14. Union Carbide Co., 'Tone M-I00 Monomer Caprolactone Acrylate Monomer for Radiation Curing' , UCAR Coatings Resins, CT 06817-0001, Danbury (1987)
  15. S. Guo, U. S. Patent, 5,646,213A (1987)
  16. S. J. Kim, Ph. D. Dissertation, Myongji Univ., Yongin, Korea (1998)
  17. J. R. Fried, 'Polymer Science and Technology', p. 161, Prentice-Hall International, Inc., New Jersey (1995)
  18. S. Zhu, Y. Tian, A. E. Hamielec, and D. R. Eaton, Macromolecules, 23(4), 1144 (1990) https://doi.org/10.1021/ma00206a037
  19. O. Yasufumi, A. Takeshi, and W. Koichiro, J. Rheal., 31(3), 251 (1987) https://doi.org/10.1122/1.549924
  20. H. R. Kricheldorf, 'Handbook of Polymer Synthesis' , Part A, pp. 713-721, Marcel Dekker, Inc., New York (1992)
  21. K. J. Ha, M. S. Dissertation, Myongji Univ., Yongin, Korea (1998)
  22. Y. Otsubo, T. Amari, K. Watanabe, and T. Nakamichi, J. Rheol., 31(3), 251 (1987) https://doi.org/10.1122/1.549924
  23. S. Paul, J. Coat. Techol., 54(692), 59 (1982)