Aromatic thermosetting copolyester nanocomposite foams: High thermal and mechanical performance lightweight structural materials

In this study, we present carbon nanoparticle incorporated high-performance aromatic thermosetting copolyester (ATSP) nanocomposite foams. The ATSP nanocomposite foams were fabricated through a facile solid-state mixing method wherein carboxylic acid and acetoxy-functional group oligomers were initi...

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Veröffentlicht in:Polymer (Guilford) 2017-08, Vol.123, p.311-320
Hauptverfasser: Bakir, Mete, Meyer, Jacob L., Economy, James, Jasiuk, Iwona
Format: Artikel
Sprache:eng
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Zusammenfassung:In this study, we present carbon nanoparticle incorporated high-performance aromatic thermosetting copolyester (ATSP) nanocomposite foams. The ATSP nanocomposite foams were fabricated through a facile solid-state mixing method wherein carboxylic acid and acetoxy-functional group oligomers were initially combined with chemically pristine carbon nanofillers separately, while in powder form. The mixtures were then subjected to a thermal condensation polymerization reaction in which the constituent oligomers formed the ester backbone of the ATSP matrix and advanced the molecular weight while acetic acid was emitted as the by-product, and generated a porous nanocomposite morphology. As compared to a neat ATSP foam, the nanocomposite foams exhibited a reduced coefficient of thermal expansion by 25% to 75 × 10−6 °C−1. Thermal stability temperature at 5% mass loss was increased by 30 °C exceeding 500 °C. Compressive mechanical strength was enhanced two-fold, reaching 16 MPa along with a nearly doubled fracture strain, which ultimately yielded improved material toughness. [Display omitted] •Facile fabrication of carbon nanofiller incorporated polymer nanocomposite foams.•Homogenous distribution of nanofillers in the matrix enabled via solid state mixing.•Characterization of cure and post-cure behaviors influenced by the nanofillers.•Characterization of thermal expansion, thermal degradation, and compressive strength.
ISSN:0032-3861
1873-2291
DOI:10.1016/j.polymer.2017.07.030