Search

To provide molecular‐scale insight into the structural evolution from tris(methylamino)borane to boron nitride (BN) fiber during the chemical thermal‐treating process, polymeric green fiber is cured in hot synthetic air at 300°C and then treats to 400, 600, 800, and 1000°C in ammonia. The chemical composition and structure of the volatile compounds and residual products are analyzed during the pyrolysis process for the polymeric green fiber. It is demonstrated that oxygen can be used to cure polymeric green fiber rapidly under the premise of ensuring a final fiber content of less than 1 wt% carbon and 2 wt% oxygen while maintaining the fiber tensile strength at 1000°C. The molecular structure evolution during the pyrolysis process for polymeric green fiber after oxygen curing is determined. Specifically, in hot synthetic air, introducing oxygen and releasing methylamine generates a B–O six‐membered ring structure in the polymer in the first stage. Then, the removal of methyl results in the formation of a B–N–O network in hot ammonia. Afterward, nitridation of the B–O six‐membered ring promotes the evolution of the B–N six‐membered ring structure with the release of water and carbon dioxide. Finally, the growth and rearrangement of the BN structure are achieved. [ABSTRACT FROM AUTHOR]

Oxygen plays a crucial role in the synthesis of boron nitride (BN) and the preparation of BN ceramics. The effects of oxygen content on the microstructure and properties of BN fibers treated at 1600 °C have not been studied yet. In this work, polymer-derived BN fibers are cured at 300 °C under oxygen and pyrolyzed at 600 °C, 700 °C and 800 °C under ammonia as the pre-heated BN fibers. Then, these pre-heated BN fibers are treated at 1600 °C under nitrogen as the final BN fibers. The compositions and microstructures of the pre-heated and final BN fibers are investigated. As the pre-heated temperature increases, the oxygen contents of the pre-heated BN fibers decrease to 24 wt%, 17 wt% and 5 wt%, respectively. The structures of the pre-heated BN fibers transform from amorphous BN to turbostratic BN. The oxygen in the pre-heated BN fiber volatilizes as boron oxide during treatment at 1600 °C, promoting the formation and growth of h-BN in the final BN fiber, with the maximum grain size reaching 74 × 20 nm (La × Lc). As the grain size of the final BN fiber increases, the Young's modulus, density and oxidation resistance level of the BN fiber improve, and the dielectric properties decrease. The final BN fiber that underwent pre-heating at 700 °C has the best comprehensive properties, with a tensile strength of 1.11 GPa and a Young's modulus of 265 GPa. This study researches the relationship between composition, structure and performance, and provides a scientific basis for the preparation process of BN fibers. • The initial BN fibers with gradient oxygen content are obtained by controlling the nitridation temperature after air curing. • The higher the oxygen content in the initial BN fibers, the better the crystallinity of the BN fibers treating at 1600 °C. • The tensile strength of BN fiber with a grain size of 34 × 11 nm (La × Lc) is 1.11 GPa, and the Young's modulus is 265 GPa. [ABSTRACT FROM AUTHOR]