Poly(phenylene-carborane) for boron-carbide/carbon ceramic precursor synthesized via nickel catalysis
High thermally and thermo-oxidatively stable poly(phenylene-carborane) (PPB) was synthesized via Ni(0)-catalyzed polymerization of bis(aryl chloride) monomer containing carborane. This polymer was soluble in THF and NMP at room temperature, thus allowing molecular weight and spectroscopic analysis....
Gespeichert in:
Veröffentlicht in: | Polymer (Guilford) 2017-04, Vol.115, p.224-231 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
Zusammenfassung: | High thermally and thermo-oxidatively stable poly(phenylene-carborane) (PPB) was synthesized via Ni(0)-catalyzed polymerization of bis(aryl chloride) monomer containing carborane. This polymer was soluble in THF and NMP at room temperature, thus allowing molecular weight and spectroscopic analysis. Number-average molecular weight determined by 1H-NMR spectroscopy was 5.4 × 103 g/mol. The crystalline character of PPB was verified by XRD analysis. This polymer exhibited excellent thermal and thermo-oxidative stability with 5% weight loss temperature to be 707 °C and >1000 °C in nitrogen and air, respectively. High char yields of 93.2% and 97.9% were obtained at 1000 °C in nitrogen and air, respectively. Additionally, PPB has proven to be excellent sing-source precursor to boron-carbide/carbon ceramic materials with high ceramic yields in the range of 91.1%–92.6%. According to XRD analysis, boron carbide crystallization for PPB occurred between 1000 and 1200 °C.
[Display omitted]
•A poly(phenylene-carborane) (PPB) was synthesized via Ni(0)-catalyzed polymerization.•PPB exhibited excellent thermal and thermo-oxidative stability.•PPB has proven to be excellent precursors to boron-carbide/carbon ceramic materials.•The ceramics showed excellent thermo-oxidative stability. |
---|---|
ISSN: | 0032-3861 1873-2291 |
DOI: | 10.1016/j.polymer.2017.03.036 |