Abstract
A series of tetra-functional fluorene-based benzoxazines containing both flexible linear aliphatic chain and rigid aromatic structure in their backbones were synthesized using mixed amines such as aniline and n-octylamine, 2,7-dihydroxy-9,9-bis-(4-hydroxyphenyl)fluorene (THPF) and paraformaldehyde as raw materials via Mannich reaction. The prepared benzoxazine monomers were identified by fourier transform infrared spectroscopy (FTIR), hydrogen nuclear magnetic resonance (1H NMR). In addition, the curing behavior, curing kinetics and rheological properties of these monomers as well as the thermal and mechanical properties of their cured resins were studied using a rheometer, differential scanning calorimeter (DSC), thermogravimetric analyzer (TGA), and dynamic thermomechanical analyzer (DMA). The newly developed benzoxazines show good processibility, excellent thermal stability and high glass transition temperature (Tg) values ranging from 291 to 307°C. By varying the proportion of n-octylamine to aniline, the properties of these resins are tuned.
Published Version
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