High glass transition catalyst-free polybenzoxazine vitrimer through one-pot solventless method

Date published

2025-04

Free to read from

2025-02-14

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Journal Title

Journal ISSN

Volume Title

Publisher

Elsevier

Department

Type

Article

ISSN

1381-5148

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Citation

Anagwu FI, Dossi E, Skordos AA. (2025) High glass transition catalyst-free polybenzoxazine vitrimer through one-pot solventless method. Reactive and Functional Polymers, Volume 209, April 2025, Article number 106186

Abstract

A high glass transition polybenzoxazine has been synthesised by a one-pot solventless method via the Mannich condensation of a phenolic disulphide, paraformaldehyde and aniline. The solventless process reduces synthesis time, material costs, and the need for post-synthesis purification. The polybenzoxazine exhibits a glass transition temperature (Tg) of 155 °C and thermosetting behaviour below this temperature. Dynamic disulphide bond metathesis associated with a topological freezing temperature of 78 °C and an activation energy of 127 kJ/mol delivers vitrimeric functionality with fast, catalyst-free stress relaxation above Tg. This material fully relaxes stress within 5 s at 190 °C, with thermal degradation beginning above 250 °C. It exhibits a glassy modulus of 3.6 GPa, high char yield (57.4 %) translating to a high limiting oxygen index (LOI) of 40.5 % and excellent environmental resistance, as evidenced by low water uptake (1.4 %) after immersion at 75 °C for 31 days. The combination of environmental resistance, due to thermosetting character, high glass transition, facile synthesis, high char yield, good processability, and fast stress relaxation position this polybenzoxazine as a promising candidate matrix system for repairable aerospace thermosetting continuous fibre composites.

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Software Description

Software Language

Github

Keywords

Polybenzoxazine; Vitrimer; Aerospace; Composites, 3403 Macromolecular and Materials Chemistry, 34 Chemical Sciences, Polymers, 3403 Macromolecular and materials chemistry, 4004 Chemical engineering

DOI

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Attribution 4.0 International

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Funder/s

Tertiary Education Trust Fund
This research was supported by the Tertiary Education Trust Fund, Nigeria, through the overseas scholarship award grant reference TETF/ES/POLY/IMO STATE/TSAS/2019/VOL.I.