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Experimental and Computational Approaches to Sulfonated Poly(arylene ether sulfone) Synthesis Using Different Halogen Atoms at the Reactive Site.
Jang, Seol; Cha, Jung-Eun; Moon, Seung Jae; Albers, Justin Georg; Seo, Min Ho; Choi, Young-Woo; Kim, Jong Hak.
Afiliación
  • Jang S; Fuel Cell Research and Demonstration Center, Future Energy Research Division, Korea Institute of Energy Research, Daejeon 56332, Republic of Korea.
  • Cha JE; Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonseiro, Seodaemun-gu, Seoul 03722, Republic of Korea.
  • Moon SJ; Fuel Cell Research and Demonstration Center, Future Energy Research Division, Korea Institute of Energy Research, Daejeon 56332, Republic of Korea.
  • Albers JG; Department of Chemical and Biomolecular Engineering, Yonsei University, 50 Yonseiro, Seodaemun-gu, Seoul 03722, Republic of Korea.
  • Seo MH; Fraunhofer Institute for Manufacturing Technology and Advanced Materials IFAM, Winterbergstrasse 28, 01277 Dresden, Germany.
  • Choi YW; Department of Nanotechnology Engineering, Pukyong National University, 45 Yongso-ro, Nam-gu, Busan 48547, Republic of Korea.
  • Kim JH; Fuel Cell Research and Demonstration Center, Future Energy Research Division, Korea Institute of Energy Research, Daejeon 56332, Republic of Korea.
Membranes (Basel) ; 12(12)2022 Dec 19.
Article en En | MEDLINE | ID: mdl-36557194
Engineering thermoplastics, such as poly(arylene ether sulfone), are more often synthesized using F-containing monomers rather than Cl-containing monomers because the F atom is considered more electronegative than Cl, leading to a better condensation polymerization reaction. In this study, the reaction's spontaneity improved when Cl atoms were used compared to the case using F atoms. Specifically, sulfonated poly(arylene ether sulfone) was synthesized by reacting 4,4'-dihydroxybiphenyl with two types of biphenyl sulfone monomers containing Cl and F atoms. No significant difference was observed in the structural, elemental, and chemical properties of the two copolymers based on nuclear magnetic resonance spectroscopy, Fourier transform infrared spectroscopy, thermogravimetric analysis, X-ray diffraction, transmission electron microscopy, and electrochemical impedance spectroscopy. However, the solution viscosity and mechanical strength of the copolymer synthesized with the Cl-terminal monomers were slightly higher than those of the copolymer synthesized with the F-terminal monomers due to higher reaction spontaneity. The first-principle study was employed to elucidate the underlying mechanisms of these reactions.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Membranes (Basel) Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Membranes (Basel) Año: 2022 Tipo del documento: Article