Multi-phenyl structured aromatic hydrocarbon polymer

Authors

  • MA Hossain Department of Chemistry, Jagannath University, Dhaka-1100, Bangladesh
  • - Morium Department of Chemistry, Jagannath University, Dhaka-1100, Bangladesh
  • M Elias Department of Chemistry, Jagannath University, Dhaka-1100, Bangladesh
  • MM Rahman Department of Chemistry, Jagannath University, Dhaka-1100, Bangladesh
  • MM Rahaman Department of Polymer, Bangladesh Council of Scientific and Industrial Research (BCSIR), Dhaka 1205, Bangladesh
  • MS Ali Department of Chemistry, Jagannath University, Dhaka-1100, Bangladesh
  • MA Razzak Department of Chemistry, Jagannath University, Dhaka-1100, Bangladesh

DOI:

https://doi.org/10.3329/bjsir.v55i2.47634

Keywords:

Multi-phenyl; Aromatic hydrocarbon polymer; Condensation polymerization; Thermooxidative stability; Inherent viscosity

Abstract

Multi-phenyl structured random polymer was synthesized via condensation polymerization reaction by applying different monomer ratios and characterized by various spectroscopic methods (FT-IR, 1H NMR). The prepared polymers showed good thermooxidative stability up to 400 ºC. The surface morphology was studied by FESEM that showed the good linkage among the polymer chains. The EDS data of poly(fluorenylene ether ketone), PFEK; demonstrated that all the monomers participated in the copolymerization reaction. Inherent viscosity values of the polymers were obtained in the range of 0.76∼1.12 dL g-1. The polymers’ yield was within 85~90%. The obtained results indicate that the multi-phenyl structured polymer will be the good candidates to prepare the effective aromatic hydrocarbon polymer electrolyte membrane.

Bangladesh J. Sci. Ind. Res.55(2), 139-146, 2020

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Published

2020-06-16

How to Cite

Hossain, M., Morium, .-., Elias, M., Rahman, M., Rahaman, M., Ali, M., & Razzak, M. (2020). Multi-phenyl structured aromatic hydrocarbon polymer. Bangladesh Journal of Scientific and Industrial Research, 55(2), 139–146. https://doi.org/10.3329/bjsir.v55i2.47634

Issue

Vol. 55 No. 2 (2020)

Section

Articles

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