Article
  • Preparation and Characterization of Photochromic Organic-Inorganic Hybrid Coating Using 1,2-Bis(2,4-dimethyl-5-phenyl-3-thienyl)3,3,4,4,5,5-hexafluoro-1-cyclopentene
  • Lee CH, Lee SG, Lee JD
  • 1,2-Bis(2,4-dimethyl-5-phenyl-3-thienyl)-3,3,4,4,5,5-hexafluoro-1-cyclopentene을 사용한 유-무기 혼성 광 변색 코팅 막의 제조 및 특성
  • 이창호, 이상구, 이종대
Abstract
Organic-inorganic hybrid coating film using 1,2-bis(2,4-dimethyl-5-phenyl-3-thienyl)-3,3,4,4,5,5-hexafluoro-1-cyclopentene (BTHFC) as a photochromic material was prepared under various reaction conditions such as the amounts of tetramethoxysilane (TMOS), various silane coupling agents, and solvent. It was found that color-fading speed and absorbance of the coating film was strongly dependent upon the polarity of silane coupling agent and solvent. In addition, the mole ratio of TMOS and methacryloyloxypropyltrimethoxysilane (MPTMS) was an important factor to determine color-fading speed and absorbance of the coating film. With increasing TMOS contents in coating film, the pencil hardness was increased. On the other hands, the transmittance of coating film was relatively decreased with the increase of TMOS.

광 변색 물질로 1,2-bis(2,4-dimethyl-5-phenyl-3-thienyl)-3,3,4,4,5,5-hexafluoro-1-cyclopentene(BTHFC)를 사용하는 유-무기 혼성 코팅막이 금속 알콕사이드인 tetramethoxysilane(TMOS), 다양한 실란 커플링제, 그리고 용매와 같은 다양한 반응 조건하에서 제조되었다. 제조된 코팅 막 중에서 상대적으로 비극성인 실린 커플링제를 사용한 경우, 광 변색 유기물인 BTHFC는 우수한 흡광도 및 소색속도를 나타내었다. 더욱이 용매 THF 존재 하에서 TMOS와 methacryloyloxypropyltrimethoxysilane(MPTMS)의 몰 비가 1:1로 하여 제조되었을 때 흡광도와 소색속도는 크고 빠른 것을 알 수 있었다. 연필강도는 TMOS의 함량이 증가할수록 증가한 반면, 투과도는 상대적으로 감소하였다.

Keywords: photochromic; 1,2-bis(2,4-dimethyl-5-phenyl-3-thienyl)-3,3,4,4,5,5-hexafluoro-1-cyclopentene; sol-gel; organic-inorganic hybrid coating.

  • Polymer(Korea) 폴리머
  • Frequency : Bimonthly(odd)
    ISSN 0379-153X(Print)
    ISSN 2234-8077(Online)
    Abbr. Polym. Korea
  • 2023 Impact Factor : 0.4
  • Indexed in SCIE

This Article

  • 2012; 36(1): 16-21

    Published online Jan 25, 2012

  • 10.7317/pk.
  • Received on May 6, 2011
  • Revised on Nov 30, -0001
  • Accepted on Jul 12, 2011

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