• Synthesis and Properties of Photocurable Epoxy Modified Acrylates Using Half-Ester Acrylates
  • Kim DK, Lim JK, Kim WG, Haw JR
  • 하프-에스터 아크릴레이트를 이용한 광경화형 에폭시 변성 아크릴레이트의 합성과 물성
  • 김동국, 임진규, 김우근, 허정림
Abstract
Various half-ester acrylates were prepared from anhydrides and 2-hydroxyethyl acrylate. Photocurable epoxy modified acrylates were prepared from synthesized half-ester acrylate and neopentylglycol diglycidylether. Physical properties such as hardness, yellowing, tensile strength and elongation were tested and compared as the structure of oligomer in cured-film differs. It was found that viscosity of neopentylglycol diglycidylether-hexahydrophthalic anhydride (NP-HA) was highest. Hardness and tensile strength of photocrosslinked neopentylglycol diglycidylether-hexahydrophthalic anhydride were better than those of other photocrosslinked epoxy acrylates. And 5% weight loss temperature of photocrosslinked neopentylglycol diglycidylether-hexahydrophthalic anhydride was higher than those of other photocrosslinked epoxy acrylates. Value of yellow index of photocrosslinked neopentylglycol diglycidyl ether-succinic anhydride (NP-SA) was lower than the other products.

다양한 하프-에스터 아크릴레이트를 합성하기 위하여 다양한 산 무수물에 2-하이드록시에틸 아크릴레이트 (2-hydroxyethyl acrylate)를 반응시켰다. 합성된 하프-에스터 아크릴레이트에 지방족 에폭시 화합물인 네오펜틸글리콜 디글리시딜에테르 (neopentylglycol diglycidylether)를 반응시켜 광경화형 에폭시 변성 아크릴레이트를 제조하였다. 점도는 헥사하이드로프탈산 무수물 (hexahydrophthalic anhydride)을 사용하여 반응시킨 네오펜틸글리콜 디글리시딜에테르-헥사하이드로프탈산 무수물 (NP-HA)이 가장 높았다. 또한 헥사하이드로프탈산 무수물을 사용한 네오펜틸글리콜 디글리시딜에테르-헥사하이드로프탈산 무수물의 광경화물은 비교적 다른 산 무수물을 사용하여 제조한 에폭시 변성 아크릴레이트의 광경화물보다 경도, 인장 강도가 우수하였으며, 5% 무게 감소 온도도 높은 것으로 보아 열적으로 안정하다는 것을 알 수 있었다. 황변 지수값은 숙신산 무수물 (succinic anhydride)을 사용하여 반응시킨 네오펜틸글리콜 디글리시딜에테르-숙신산 무수물 (NP-SA)이 가장 낮았다.

Keywords: epoxy acrylate; photocurable; 2-hydroxyethyl acrylate; half-ester acrylate

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  • Polymer(Korea) 폴리머
  • Frequency : Bimonthly(odd)
    ISSN 0379-153X(Print)
    ISSN 2234-8077(Online)
    Abbr. Polym. Korea
  • 2024 Impact Factor : 0.6
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This Article

  • 2004; 28(6): 531-537

    Published online Nov 25, 2004

  • Received on Aug 23, 2004
  • Accepted on Nov 19, 2004