4.8 Article

Polyimide Hybrid Nanocomposites with Controlled Polymer Filling and Polymer-Matrix Interaction

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 14, Issue 24, Pages 28239-28246

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c02575

Keywords

polyimide; hybrid nanocomposites; polymer confinement; fracture resistance; molecular bridging; polymer-surface interaction

Funding

  1. Air Force Office of Scientific Research (AFOSR) [FA9550-12-1-0120]
  2. National Science Foundation [ECCS-1542152]

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This study presents an easier approach to fabricate polyimide nanocomposites with enhanced fracture resistance by cross-linking shorter preimidized polyimide chains filled in a nanoporous matrix. The higher chain mobility and stronger polymer-surface interaction achieved with this method significantly improve the fracture resistance of the nanocomposite.
Polyimide hybrid nanocomposites with the polyimide confined at molecular length scales exhibit enhanced fracture resistance with excellent thermal-oxidative stability at low density. Previously, polyimide nanocomposites were fabricated by infiltration of a polyimide precursor into a nanoporous matrix followed by sequential thermally induced imidization and cross-linking of the polyimide under nanometer-scale confinement. However, byproducts formed during imidization became volatile at the cross-linking temperature, limiting the polymer fill level and degrading the nanocomposite fracture resistance. This is solved in the present work with an easier approach where the nanoporous matrix is filled with shorter preimidized polyimide chains that are cross-linked while in the pores to eliminate the need for confined imidization reactions, which produces better results compared to the previous study. In addition, we selected a preimidized polyimide that has a higher chain mobility and a stronger interaction with the matrix pore surface. Consequently, the toughness achieved with un-cross-linked preimidized polyimide chains in this work is equivalent to that achieved with the cross- linking of the previously used polyimide chains and is doubled when preimidized polyimide chains are cross-linked. The increased chain mobility enables more efficient polymer filling and higher polymer fill levels. The higher polymer-pore surface interaction increases the energy dissipation during polyimide molecular bridging, increasing the nanocomposite fracture resistance. The combination of the higher polymer fill and the stronger polymer-surface interaction is shown to provide significant improvements to the nanocomposite fracture resistance and is validated with a molecular bridging model.

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