Synthesis and Characteristics of Aminated Poly(arylene ether sulfone) as Thermostable Anion Exchanger

내열성 음이온교환수지로서 Aminated Poly(arylene ether sulfone)의 합성과 물성

  • 손원근 (충남대학교 고분자공학과) ;
  • 유현지 (충남대학교 고분자공학과) ;
  • 황택성 (충남대학교 화학공학과) ;
  • 김동철 (충남대학교 섬유공학과) ;
  • 김상헌 (한밭대학교 응용화학공학부) ;
  • 송해영 (충남대학교 고분자공학과)
  • Published : 2002.01.01

Abstract

In this study, poly(arylene ether sulfone) (PAES) having thermal stability and excellent mechanical properties was synthesized to be useful for the matrix of anion exchange resin. $1^{\circ}$-Aminated poly(arylene ether sulfone) ($1^{\circ}$-APAES) was prepared by reduction reaction after lithiation of PAES. Then $3^{\circ}$-APAES was Prepared by alkylation of the amino group of $1^{\circ}$-APAES. The structures of PAES and APAESs were confirmed with FT-IR and $^1H-NMR$ spectroscopy. Also, thermal properties of the resins were characterized by DSC and TG analysis. The introduction of amine groups in PAES resulted in the increase of glass transition temperature and decrease of initial thermal degradation temperature. The ion exchange capacities of $1^{\circ}$-APAES and $1^{\circ}$-APAES were 1.19 and 1.45 meq/g, respectively.

열 안정성과 우수한 기계적 성질을 갖는 poly(arylene ether sulfone) (PAES)을 음이온교환수지의 지지체로 이용하였다. $1^{\circ}$-Aminated poly(arylene ether sulfone) ($1^{\circ}$-APAES)은 PAES을 리튬화한후 환원 반응시켜 제조하였고, $3^{\circ}$-APAES의 아민기를 알킬화 반응시켜 제조하였다. PAES와 APAES들의 구조는 FT-IR과 H$^1$-NMR으로 확인하였고, 열적 특성은 DSC와 TG 분석을 통하여 조사하였다. PAES에 아민기가 도입됨에 따라 $T_g$는 증가하였고, 초기 열분해 온도는 감소하였다. $1^{\circ}$-APAES과 $3^{\circ}$-APAES의 이온교환용량은 각각 1.19와 1.45 meq/g 이었다.

Keywords

References

  1. Polym. Sci. and Tech.(Korea) v.8 no.596 N.S. Cho;K.P. Lim
  2. J. Membr. Sci. v.49 no.121 Y. Mizutani
  3. J. Soc. Chem. Ind. v.54 no.1 B.A. Adams;E.L. Holmes
  4. Ion Exchange in Analytical Chemistry H.F. Walton;R.D. Rocklin
  5. Ion Exchange Separations in Analytical Chemistry O. Samuelson
  6. Ion Exchange F. Helfferich
  7. Macromol. Chem. v.184 no.779 W. Koch;W. Heitz
  8. J. Polym. Sci. Part A: Polym. Chem. v.31 no.853 M. Ueda;H. Toyota;T. Ouchi;J.I. Sugiyama;K. Yonetake;T. Masuko;T. Teramoto
  9. Ind. Eng. Chem. Res. v.36 K. Miyataka;H. Iyotani;K. Yamamoto;E. Tsuchida
  10. Polymer(Korea) v.23 no.1 Y.U. Kang;T.S. Hwang;H.Y. Song;W.K. Son;J.K. Park
  11. Purification of Laboratory Chemicals(3rd) B.D. Perrin;W.L.F. Armarego
  12. Macromolecules v.28 no.294 Michael D. Guiver;Gilles P. Robertston
  13. Macromolecules v.28 Michael D. Guiver;P. Robertston;Stephen Floey https://doi.org/10.1021/ma00127a005
  14. Simple Ion Exchange Equilibria V.S. Soldatov;H.B. Malaova(ed.)
  15. Reactive Polym. v.19 no.105 V.S. Soldatov