4.7 Article

Synthesis of the sulfonated poly(ether ether ketone ketone) proton exchange membrane with butane-1,4-diylbis(oxy) spacers and sulfopropyloxy pendants through Friedel-Crafts polyacylation

Journal

INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
Volume 46, Issue 54, Pages 27770-27783

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2021.06.022

Keywords

Proton exchange membrane fuel cells; Sulfonated poly(ether ether ketone ketone); Friedel-crafts polyacylation; Nanophase separation; Butane-1,4-diylbis(oxy) spacer

Funding

  1. National Natural Science Foun-dation of China [21376147, 21573143, 21706156]
  2. NSAF [U1630102]
  3. Research Fund program of Key laboratory of Fuel Cell Tech-nology of Guangdong Province

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The translation describes the synthesis method and characteristics of a novel proton exchange membrane, which has high proton conductivity, moderate water uptake, and high ion exchange capacity, attributed to the features of flexible spacers and sidechains.
A novel proton exchange membrane composed of the sulfonated poly(ether ether ketone ketone) (SPEEKK) with butane-1,4-diylbis(oxy) spacers in the backbone and sulfopropyloxy pendants is synthesized through the Friedel-Crafts polyacylation of 1,4-diphenoxybutane (DPB), diethyl-3,3'-([1,1'-biphenyl]-2,2'-diylbis(oxy))bis(propane-1-sulfonate) (SBP-OEt), and terephthaloyl chloride (TPC) under mild conditions. The monomer DPB can introduce the flexible aliphatic butane-1,4-diylbis(oxy) spacers into the polymeric backbone and thus promote the formation of proton transport channels. The as-synthesized SPEEKK exhibits a high proton conductivity of 152.5 mS cm(-1) at 95 degrees C and 90% relative humidity (RH), a moderate water uptake of 53.2% at 100 degrees C and also a high ion exchange capacity of 1.74 mmol g(-1). These characteristics are attributed to the enhanced nanophase separation induced by the flexible butane-1,4-diylbis(oxy) spacers and hydrophilic sulfopropyloxy sidechains. (C) 2021 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.

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