DOI QR코드

DOI QR Code

Preparation of Transparent Film by Coating of Acrylate Copolymer as MMA-co-GMA-co-AA

(MMA-co-GMA-co-AA)형 아크릴레이트 공중합체를 도포한 투명필름의 제조

  • Kim, Ji-Hye (Department of Chemical Engineering, Sungkyunkwan University) ;
  • Kim, Moon-Sun (Bio/Nano-Fusion Material Research Center, Sungkyunkwan University) ;
  • Hong, Sung-Chul (Department of Chemical Engineering, Sungkyunkwan University) ;
  • Kim, Byung-Woo (Department of Chemical Engineering, Sungkyunkwan University)
  • 김지혜 (성균관대학교 화학공학과) ;
  • 김문선 (성균관대학교 바이오/나노융합재료연구단) ;
  • 홍성철 (성균관대학교 화학공학과) ;
  • 김병우 (성균관대학교 화학공학과)
  • Published : 2011.01.30

Abstract

In the study, acrylate copolymer as MMA-co-GMA-co-AA with a high hardness and flexibility was synthesized for applying to the clear protection film, where GMA was used as a mediator to enhance polymerization-efficiency between MMA and AA. With an increase of GMA content, molecular weight and hardness of acrylate copolymer increased, however, flexibility decreased. With an increase of AA content, its molecular weight and hardness decreased, however, flexibility increased. Molar ratio of GMA/MMA and AA/GMA were optimized as 1.6 and 1.8, respectively, at 30 g of MMA to enhance hardness and flexibility of acrylate copolymer film. Molecular weight and Tg of the acrylate copoylmer were 13,300 g/mol and 136.5 $^{\circ}C$, respectively. Hardness of the coated film at 1.4 g/$m^2$ of spread was 1 H and no crack was observed at expansion ratio of 5% and 15%, respectively. Hardness of film was improved to 3 H by increasing spread of 4.1-4.6 g/$m^2$.

본 연구에서는 투명 보호필름에 적용할 수 있는 내구성과 연신성이 우수한(MMA-co-GMA-co-AA) 형의 아크릴레이트 공중합체를 합성하였으며 MMA와 AA 간의 중합효율을 높이기 위하여 GMA를 매개제로 선택하였다. GMA의 함량이 증가할수록 아크릴레이트 공중합체의 분자량과 내구성은 개선되었으나 연신성은 떨어졌고 AA의 함량이 증가할수록 공중합체의 분자량과 내구성은 낮아졌으나 반대로 연신성은 개선되었다. MMA의 함량이 30 g인 조건에서, 아크릴레이트 공중합체 막의 내구성과 연신성을 개선할 수 있는 GMA/MMA의 최적 몰 비는 1.6, AA/GMA의 최적 몰비는 1.8이였으며 공중합체의 평균분자량과 Tg는 각각 13,300 g/mol, 136.5 $^{\circ}C$였다. 아크릴레이트 공중합체를 1.4 g/$m^2$ 도포된 필름의 표면경도는 1 H였으며 5, 15% 연신조건에서 연신성이 모두 양호하였다. 도포량을 4.1-4.6 g/$m^2$으로 높으면 표면경도는 3 H로 개선되었다.

Keywords

References

  1. Kardar, P., Ebrahimi, M., Bastanib, S. and Jalili, M., "Using Mixture Experimental Design to Study the Effect of Multifunctional Acrylate Monomers on UV Cured Epoxy Acrylate Resins," Prog. Org. Coat., 64(1), 74-80(2009). https://doi.org/10.1016/j.porgcoat.2008.07.022
  2. Wang, H., Xu, S. and Shi, W., "Photopolymerization Behaviors of Hyperbranched Polyphosphonate Acrylate and Properties of the UV Cured Film," Prog. Org. Coat., 65(4), 417-424(2009). https://doi.org/10.1016/j.porgcoat.2009.03.005
  3. Do, H. S., Kim, D. J. and Kim, H. J., "Application of UV-Curable Materials," J. Adhes. Interface, 4(3), 41-51(2003).
  4. Kim, U. Y. and Huang, R. Y., "Hydrophilic Polymer Membranes Containing Carboxylic Groups," Eur. Polym. J., 15(4), 325-332 (1979). https://doi.org/10.1016/0014-3057(79)90151-4
  5. EI-Hamouly, S. H., Aziz, W., El-Shamy, E. H. and Abd-El-Nour, K. N., "Ultrasonic Detection of Photo Cross-Linking in Some Acrylate Copolymers," Polym. Degrad. Stab., 37(1), 41-49(1992). https://doi.org/10.1016/0141-3910(92)90090-R
  6. Abusafieh, A., Gobran, R and Kalidindi, S. R., "Synthesis and Characterization of a Poly(Methacrylate-Acrylic Acid) Copolymer for Biomplant Applications," J. Appl. Polym. Sci., 63(1), 75-87(1997). https://doi.org/10.1002/(SICI)1097-4628(19970103)63:1<75::AID-APP8>3.0.CO;2-P
  7. Chae, K. H. and Song, H. B., "Crosslinking Reaction of Glycidyl Methacrylate Copolymers Containing Oxime-Urethane Groups Using Photogenerated Pendant Amines," Polym. Bull., 40(6), 667-674(1998). https://doi.org/10.1007/s002890050306
  8. Gonzalez, I., Asua, J. M. and Leiza, J. R., "The Role of Methyl Methacrylate on Braching and Gel Formation in the Emulsion Copolymerization of BA/MMA," Polym., 48(9), 2542-2547(2007). https://doi.org/10.1016/j.polymer.2007.03.015
  9. Fernandez-Garcia, M., Canamero, P. F. and Fuente la de, J. L., "Synthesis and Characterization of Functional Gradient Copolyners of Glycidyl Methacrylate and Butyl Aacrylalate," React. Funct. Polym., 68(9), 1384-1391(2008). https://doi.org/10.1016/j.reactfunctpolym.2008.06.019
  10. Chang, S. T. and Chou, P. L., "Photodiscoloration Inhibition of Wood Coated with UV-Curable with UV-Curable Acrylic Clear Coatings and Its Elucidation," Polym. Degrad. Stab., 69(3), 355-360(2000). https://doi.org/10.1016/S0141-3910(00)00082-3
  11. Hwang, H. D., Choi, J. H., Moon, J. I. and Kim, H. J., "Thermal Stability and Surface Hardnees of UV-curable Epoxy Acrylate Coatings for Wooden Flooring," Mokchae Konghak, 36(6), 121-129(2008).
  12. Kim, H. J., "The Physical Properties of Polycarbonate Films Coated with Hard and Color Coating Materials," J. Kor. Chem. Eng., 47(3), 316-320(2009).
  13. Jian, Z., Yong, H., Ming, X. and Jun, N., "Preparation and Properties of Dual-Cure Polyurethane Acrylate," Prog. Org. Coat, 66(1), 35-39(2009). https://doi.org/10.1016/j.porgcoat.2009.05.001
  14. Palanisamy, A. and Rao, B. S., "Tetrafuncyional Acrylates Based on $\beta$-Hydroxy Alkyl Amides as Crosslinkers for UV Curable Coatings," Prog. Org. Coat., 56(4), 297-303(2006). https://doi.org/10.1016/j.porgcoat.2006.05.014
  15. Tasic, S., Bozic, B. and Dunjic, B., "Synthesis of New Hyperbranched Urethane-Acrylates and Their Evaluation in UV-Curable Coatings," Prog. Org. Coat, 51(4), 321-328(2004).
  16. Lim, J. K., Kim, D. K. and Hwang, J. Y., "Synthesis and Preperties of Photocurable Aliphatic Epoxy Acrylate (I)," J. Kor. Ind. Eng. Chem, 14(6), 818-823(2003).
  17. Peng, D., Zhang, X., Feng, C., Lu, G., Zhang, S. and Huang, X., "Synthesis and Characterization of Amphiphlic Graft Copolymers with Hydrophilic Poly(acrylic acid) Backbone and Hydrophobic Poly(methyl methacrylate) Side Chain," Polym., 48(18), 5250-5258(2007). https://doi.org/10.1016/j.polymer.2007.07.005
  18. Kalal, J., Svec, F. and Marousek, V., "Reactions of Epoxide Groups of Glycidyl Methacrylate Copolymers," J. Polym. Sci., 47(1), 155-166(1974).
  19. Navarro-Rodrjguez, D., Rodrjguez-Gonzqlez, F. J., Romero-Garcia, J., Jimenmz- Regaado, E. J. and Guillon, D., "Chemical Modification of Glycidyl Methacrylate Polymers with 4-Hydroxy-4'-Methoxybiphenyl Groups," Eur. Polym. J., 34(7), 1039-1045(1998). https://doi.org/10.1016/S0014-3057(97)00219-X
  20. Nakamura, Y., "Thermo and Active Energy Ray Curable Resin Composition Used for Protecting Layer of Transfer Material Transfer Material Surface Protecting Material and Process for Producing Molded Article Excellent in Abrasion Resistance and Cheminal Resistance," US Patent, No. 5,993,588(1997).
  21. Schwalm, R., "UV Coatings-Basics, Recent Denelopments and New Applications," Elesvier, Netherlands, 160-178(2007).
  22. Safa, K. D. and Nasirtabrizi, M. H., "Ring Opening Reactions of Glycidyl Methacrylate Copolymer to Introduce Bulky Oranosilicon Sside Chain Substituents," Polym. Bull., 57(3), 293-304(2006). https://doi.org/10.1007/s00289-006-0564-9
  23. Choi, Y. H., Kang, J. K. and Lee, W. K., "Effect of Functional Monomers on Pressure-Sensitive Adhesives of Acrylic Emulsion," J. Adhes. Interface, 10(1), 1-10(2009).
  24. Garay, M. T., Llamas, M. C. and Iglesias, E., "Study of Polymer-Polymer Complexes and Blends of Poly(N-Iisopropylacrylamide) with Poly(Carboxylic Acid): 1. Poly(Acrylic Acid) and Poly(Methacrylic Acid)," Polym., 38(20), 5091-5096(1997). https://doi.org/10.1016/S0032-3861(97)00060-8
  25. Schwalm, R., HauBling, L., Reich, W., Beck, E., Eeck, P., Enenkl, P. and Menzel, K., "Tuning the Mechanical Properties of UV Coatings towards Hard and Flexible Systems," Prog. Org. Coat, 32, 191-196(1997). https://doi.org/10.1016/S0300-9440(97)00060-X
  26. Choi, M. H. and Chung, I. J., "Effect of Curing Kinetics on the Cross-link Density and Mechanical Property of Resol Type of Phenolic Resin," J. Korean. Chem. Eng., 36(3), 399-406(1998).