4.7 Article

Solvent-free Synthesis of Alkynyl-Based Biobased Benzoxazine Resins with Excellent Heat Resistance

Journal

ACS APPLIED POLYMER MATERIALS
Volume 5, Issue 4, Pages 3015-3022

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsapm.3c00183

Keywords

biobased benzoxazine; solvent-less synthesis; thermal properties; mechanical properties; flame-retardant properties

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The synthesis of high-performance biomass benzoxazine resin using a solvent-free method is important for environmental sustainability and industrial application. Biobased eugenol and magnolol with allyl cross-linking sites, along with 3-aminophenylacetylene with alkynyl cross-linking sites, were used to prepare two biomass benzoxazine monomers E-apa and M-apa. The cured resins poly(E-apa) and poly(M-apa) exhibited superior properties compared to typical biobased heat-resistant benzoxazine resins, with higher glass-transition temperature (Tg) and thermal decomposition temperature (Tdi), better mechanical properties, and improved flame retardancy. These enhanced properties are attributed to the combination of multiple cross-linking sites and rigid phenol sources in poly(M-apa).
The synthesis of high-performance biomass benzox-azine resin by a solvent-free method is of great significance for environmental sustainability and practical application in the industrial field. In this paper, biobased eugenol and magnolol with additional allyl cross-linking sites were taken as phenol sources, and 3-aminophenylacetylene with alkynyl cross-linking sites was used as an amine source to prepare two biomass benzoxazine monomers E-apa and M-apa, and the corresponding cured resins poly(E-apa) and poly(M-apa) were prepared through a certain curing process. The comprehensive properties of the cured resins were studied. The results show that the glass-transition temperature (Tg) of poly(M-apa) is as high as over 400 degrees C, which is higher than that of poly(E-apa) (215 degrees C), as well as the Tg values of the typical biobased heat-resistant benzoxazine resins reported so far. At the same time, the initial thermal decomposition temperature (Tdi) of poly(M-apa) (441 degrees C) is higher than that of poly(E-apa) (373 degrees C), showing better thermostability. In addition, poly(M-apa) also exhibits better mechanical properties including higher storage modulus and tensile strength (5.03 GPa, measured at 25 degrees C, and 48.0 +/- 2.2 MPa, respectively) than poly(E-apa) (3.93 GPa and 37.5 +/- 1.5 MPa, respectively). Besides, poly(M-apa) performs better in flame retardancy. The better comprehensive properties of poly(M-apa) are based on the combined action of multiple cross-linking sites and rigid phenol sources.

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