A new fully biobased trioxazine benzoxazine is synthesized by reacting resveratrol, furfurylamine, and paraformaldehyde via the Mannich condensation reaction. The chemical structure of this biobenzoxazine is characterized by 1 H and 13 C nuclear magnetic resonance and Fourier transform infrared (FT-IR) spectroscopies. 1 H− 1 H nuclear Overhauser effect spectroscopy is utilized to unambiguously identify the isomer obtained. Monomer polymerization is investigated by differential scanning calorimetry and in situ FT-IR. Thermal stability of the fully polymerized polybenzoxazine is evaluated by thermogravimetric analysis, and flammability is assessed by microscale combustion calorimetry. The biothermoset obtained shows high thermal stability and low flammability, T d10 of 403°C and char yield of 64%, respectively, low heat release capacity (54 J/gK), and low total heat release (9.3 KJ/g), thus exhibiting self-extinguishing and nonignitable properties. Consequently, this new fully biobased trioxazine benzoxazine and its corresponding polybenzoxazine possess excellent processability and thermal properties, suggesting great potential toward high-performance and fire-resistant materials.

A fully bio-based benzoxazine containing latent catalytic system is designed and successfully synthesized and it can be used as both an initiator and a beneficial property modifier of other thermosetting systems, especially for fire related properties.

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In recent years, main-chain-type benzoxazine resins have been extensively investigated due to their excellent comprehensive properties for many potential applications. In this work, two new types of main-chain benzoxazine polymers were synthesized from daidzein, aromatic/aliphatic diamine, and paraformaldehyde. Unlike the approaches used synthesizing traditional main-chain-type benzoxazine polymers, the precursors derived from daidzein can undergo a further cross-linking polymerization in addition to the ring-opening polymerization of the oxazine ring. The structures of the new polymers were then studied by 1H nuclear magnetic resonance spectroscopy (NMR) and Fourier-transform infrared spectroscopy (FT-IR), and the molecular weights were determined by using gel permeation chromatography (GPC). We also monitored the polymerization process by differential scanning calorimetry (DSC) and in situ FT-IR. In addition, the thermal stability and flame-retardant properties of the resulting polybenzoxazines were investigated using TGA and microscale combustion calorimeter (MCC). The polybenzoxazines obtained in this study exhibited a very high thermal stability and low flammability, with a Tg value greater than 400 °C, and a heat release capacity (HRC) value lower than 30 J/(g K).