Preparation and Characteristics of Partially Fluorinated-Sulfonated Poly(biphenylene-co-sulfone)ether Membranes for Polymer Electrolyte Membrane Fuel Cell

고분자전해질 연료전지용 부분 불소계 설폰화 Poly(biphenylene-co-sulfone)ether 막의 제조와 특성

  • Park, Jae-Wan (Environment & Resources Research Center, Korea Research Institute of Chemical Technology) ;
  • Chang, Bong-Jun (Environment & Resources Research Center, Korea Research Institute of Chemical Technology) ;
  • Kim, Jeong-Hoon (Environment & Resources Research Center, Korea Research Institute of Chemical Technology) ;
  • Lee, Yong-Taek (Department of Chemical Engineering, Chungnam National University)
  • 박재완 (한국화학연구원 환경자원센터) ;
  • 장봉준 (한국화학연구원 환경자원센터) ;
  • 김정훈 (한국화학연구원 환경자원센터) ;
  • 이용택 (충남대학교 화학공학과)
  • Received : 2009.11.02
  • Accepted : 2009.11.26
  • Published : 2010.03.25

Abstract

A series of partially fluorinated, sulfonated poly(biphenylene-co-sulfone)ether containing perfluorocyclobutane(PFCB) groups were prepared for fuel cell applications through three synthetic steps: synthesis of trifluorovinylether-terminated monomers, thermal cycloaddition and post-sulfonation. Two kinds of trifluorovinylether-terminated monomers were synthesized and statistically copolymerized via thermal cycloaddition to obtain a series of polymers containing 20-60 mol% of biphenyl units(PBS-X). The post-sulfonation of PBS-X was carried out using chlorosulfonic acid(CSA) to obtain copolymers with various sulfonation levels(SPBS-X). All the synthesized compounds, monomers and polymers were characterized by $^1H$-NMR, $^{19}F$-NMR and FT-IR. It was confirmed that the ion exchange capacity(IEC), water uptake and ion conductivity of SPBS-X increased with the increment of sulfonated biphenyl units. Particularly, SPBS-60 showed higher ion conductivity compared to Nafion$^{(R)}$-115 at 25~80 $^{\circ}C$.

불소 관능기인 perfluorocyclobutane(PFCB)기를 함유하는 설폰화된 부분 불소계 poly(biphenyleneco-sulfone)ether 공중합체(SPBS-X)를 제조하였다. 제조과정은 trifluorovinylether그룹을 양 말단에 포함하는 단량체의 합성, 고리화부가 반응형태의 열중합 그리고 후설폰화(post-sulfonation)의 3단계 합성과정을 통하였다. Trifluorovinylether그룹을 양 말단에 포함하는 biphenyl계와 sulfonyl계 단량체를 합성하였고, biphenyl계의 함량을 20 mol%에서 60 mol%까지 조절하면서 고리화부가 반응형태의 열중합을 통해 랜덤 공중합체가 얻어졌다(PBS-X). 후설폰화는 chlorosulfonic acid(CSA)를 사용하여 수행되었으며, 이를 통해 다양한 설폰화도를 가지는 고분자를 합성하였다. $^1H$-NMR, $^{19}F$-NMR 및 FT-IR 분석을 통하여, 제조된 화합물, 단량체 및 중합체들이 성공적으로 합성되었음을 확인하였다. 상온에서 CSA에 대해 설폰화 활성을 가지는 biphenyl기의 함량이 증가함에 따라 이온교환능력(IEC), 함수율 및 이온전도도가 증가하는 경향을 보였고, SPBS-60의 경우 넓은 온도범위(25~80 $^{\circ}C$)에서 Nafion$^{(R)}$-115보다 높은 이온전도도(80 $^{\circ}C$: 0.08 S/cm at RH 100%)를 나타내었다.

Keywords

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