Polymers (Mar 2021)

Resin Transfer Moldable Fluorinated Phenylethynyl-Terminated Imide Oligomers with High T<sub>g</sub>: Structure–Melt Stability Relationship

  • Weijie Hong,
  • Lili Yuan,
  • Yanping Ma,
  • Chao Cui,
  • Haoyang Zhang,
  • Shiyong Yang,
  • Wen-Hua Sun

DOI
https://doi.org/10.3390/polym13060903
Journal volume & issue
Vol. 13, no. 6
p. 903

Abstract

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Phenylethynyl-terminated aromatic polyimides meet requirements of resin transfer molding (RTM) and exhibits high glass transition temperature (Tg) were prepared. Moreover, the relationship between the polyimide backbones structure and their melting stability was investigated. The phenylethynyl-terminated polyimides were based on 4,4′-(hexafluorosiopropylidene)-diphthalic anhydride (6FDA) and different diamines of 3,4′-oxydianiline (3,4′-ODA), m-phenylenediamine (m-PDA) and 2,2′-bis(trifluoromethyl)benzidine (TFDB) were prepared. These oligoimides exhibit excellent melting flowability with wide processing temperature window and low minimum melt viscosities (gs, 363–391 °C) and good tensile strength (51–66 MPa). The cure kinetics studied by the differential scanning calorimetry (DSC), 13C nuclear magnetic resonance (13C NMR) characterization and density functional theory (DFT) definitely confirmed that the electron-withdrawing ability of oligoimide backbone can tremendously affect the curing reactivity of terminated phenylethynyl groups. The replacement of 3,4′-ODA units by m-PDA or TFDB units increase the electron-withdrawing ability of the backbone, which increase the curing rate of terminated phenylethynyl groups at processing temperatures, hence results in the worse melting stability.

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