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Synthesis of h‐BN composite powders via aluminothermic reduction combustion route
h‐BN composite powders were prepared by an aluminothermic reduction combustion synthesis route using a mixture of B2O3 and Al as raw material, and MgO as diluent under low‐pressure nitrogen (.6 MPa). The phase transformation and structural evaluation during the combustion synthesis were investigated...
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Published in: | International journal of applied ceramic technology 2024-03, Vol.21 (2), p.727-740 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites |
Online Access: | Get full text |
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Summary: | h‐BN composite powders were prepared by an aluminothermic reduction combustion synthesis route using a mixture of B2O3 and Al as raw material, and MgO as diluent under low‐pressure nitrogen (.6 MPa). The phase transformation and structural evaluation during the combustion synthesis were investigated. Samples with B2O3 to Al molar ratio of 1:6 exhibited the highest diffraction peaks of h‐BN, in which the phases are h‐BN, Al2O3·7AlN, AlN, and MgAlON spinel phase. The combustion wave quenching test revealed that h‐BN is mainly formed via following routes: first, Al reacts with nitrogen; then the resulting AlN reacts with B2O3 to form h‐BN. Due to solid solution formation between Al2O3, AlN, and MgO, both MgAlON and Al2O3·7AlN were formed in the resulting samples. The composite powders obtained by aluminothermic reduction combustion synthesis in this work exhibit potential application in refractories industry for replacing graphite in carbon‐containing refractories.
h‐BN composite powders were combustion synthesized via aluminothermic reaction. Product with B2O3 to Al molar ratio of 1:6 exhibited highest h‐BN diffraction peaks. Nitriding of Al formed AlN and release heat maintaining the reaction forming h‐BN. h‐BN was mainly formed via the reaction between AlN and B2O3. The h‐BN composite powder can be used as substitution for graphite in refractories. |
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ISSN: | 1546-542X 1744-7402 |
DOI: | 10.1111/ijac.14539 |