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Synthesis of UV-Curable Modified (3,4-epoxycyclohexane)methyl 3,4-epoxycyclohexylcarboxylate Acrylate

자외선 경화형 변성 (3,4-epoxycyclohexane)methyl 3,4-epoxycyclohexylcarboxylate 아크릴레이트의 합성

  • Received : 2017.01.26
  • Accepted : 2017.03.13
  • Published : 2017.04.27

Abstract

In this study, (3,4-epoxycyclohexane)methyl 3,4-epoxycyclohexylcarboxylate acrylate was synthesized by reacting (3,4-epoxycyclohexane)methyl 3,4-epoxycyclohexylcarboxylate with acrylic acid to minimize hardening shrinkage and to improve heat resistance, which are known as disadvantages of photopolymers for 3D printing application. Urethane acrylate was synthesized by reacting 1,3,5-triazine-2,4,6-triamino alcohol, 2-hexylethyl acrylate, and isophorone diisocyanate in order to improve the mechanical properties without deteriorating the heat resistance. The physical properties before and after the synthesis of the acrylate and the mechanical properties when the urethane acrylate was applied were investigated. The reaction progress of the composite was examined by FTIR and $^{13}C$ NMR. The heat deflection temperature, flexural strength, and surface hardness of the molding were measured. The curing behavior by Photo-DSC ultraviolet irradiation was also examined.

Keywords

References

  1. 3D Printing and Additive Manufacturing State of the Industry Annual Worldwide Progress Report, p.15-64, Wohlers Associates, Inc. USA (2015).
  2. 3D Printing(Printer, Materials) Market Report, p.23-36, IRS Global, Korea (2013).
  3. S. P. Pappas, UV Curing : Science and Technology, 1th ed., p.178-211, Technology Marketing Corporation, Norwalk, CT, USA (1985).
  4. R. Holman, in Proceedings of SITA Technology, p.7-13, London (1984).
  5. M. Ueda et al, Recent Advances in UV/EB Radiation Curing Technology, p.300, CMC, Japan (2006).
  6. M. J. Moon, J. H. Park, G. D. Lee, C. S. Suh and J. R. Kim, J. Ind. Eng. Chem., 2, 175 (1991).
  7. J. B. Lee, J. H. Lee and K. C. Sung, J. Korean Oil Chem. Soc., 29, 159 (2012).
  8. H. Sasaki et al, Application of Photo-Cation Curing System of the Oxetane Compound, 2, p.4, TOAGOSEI Group Research Annual Report, Japan (1999).
  9. N. Koike, Monofunctional Oxetane Excellent Toughness, 10, p.40, Toagosei Group Research Annual Report, Japan (2007).
  10. J. M. Lee, H. P. Yi, S. G. Lee, H. N. Park and G. S. Choi, Patent(in Korea), 10-2016-0114889, Aekyung Chemical Co. Ltd., Seoul (2016).
  11. J. M. Lee, H. P. Yi, S. G. Lee, H. N. Park and G. S. Choi, Patent(in Korea), 10-2016-0114893, Aekyung Chemical Co. Ltd., Seoul (2016).
  12. M. J. Han and H. H. Lim, Patent(in Korea), 10-1569-3440000, Korea Research Institute of Chemical Technology, Daejeon (2015).
  13. H. N. Park, J. M. Lee, H. P. Yi and G. S. Choi, Patent(in Korea), 10-2016-0058958, Aekyung Chemical Co. Ltd., Seoul (2016).
  14. ASTM D648-16, Standard Test Method for Deflection Temperature of Plastics Under Flexural Load in the Edgewise Position, ASTM International, West Conshohocken, PA, 2016, www.astm.org
  15. ASTM D790-15e2, Standard Test Methods for Flexural Properties of Unreinforced and Reinforced Plastics and Electrical Insulating Materials, ASTM International, West Conshohocken, PA, 2015, www.astm.org
  16. ASTM D2240-15, Standard Test Method for Rubber Property-Durometer Hardness, ASTM International, West Conshohocken, PA, 2015, www.astm.org