Boron nitride nanotubes and process for production thereof
US-2016083253-A1 · Mar 24, 2016 · US
US12286347B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-12286347-B2 |
| Application number | US-201816647959-A |
| Country | US |
| Kind code | B2 |
| Filing date | Sep 18, 2018 |
| Priority date | Sep 21, 2017 |
| Publication date | Apr 29, 2025 |
| Grant date | Apr 29, 2025 |
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The present application relates to boron nitride nanotube (BNNT)-nanoparticle composites, to methods of preparing such composites and their use, for example, in metal/ceramic matrix composites and/or macroscopic assemblies. For example, the methods comprise subjecting a source of hydrogen, a source of boron, a source of nitrogen and a nanoparticle precursor to a stable induction thermal plasma and cooling the reaction mixture to obtain the composite.
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The invention claimed is: 1. A method for preparing a boron nitride nanotube (BNNT)-nanoparticle composite, the method comprising: subjecting a source of hydrogen, a source of boron, a source of nitrogen and a nanoparticle precursor that is a non-catalytic metal or a non-catalytic ceramic to a stable induction thermal plasma to form a reaction mixture in the plasma; and cooling the reaction mixture to obtain the BNNT-nanoparticle composite with nanoparticles attached to on outer surface of BNNTs. 2. The method of claim 1 , wherein the stable induction thermal plasma has a plasma temperature of about 1,000 K to about 10,000 K. 3. The method of claim 1 , wherein the reaction mixture is formed in the plasma at a pressure of less than 2 atm. 4. The method of claim 1 , wherein (a) the source of boron is boron nitride, elemental boron, borane, ammonia borane (borazane), borazine, a boron trihalide, a metal boride or mixtures thereof; (b) the source of nitrogen is boron nitride, N 2 , NH 3 , NH 4 OH, borazane, borazine or mixtures thereof; and/or (c) the source of hydrogen is H 2 , NH 3 , NH 4 OH, borane, borazane, borazine or mixtures thereof. 5. The method of claim 1 , wherein the nanoparticle precursor is a metal ceramic, or a metallic element or alloy. 6. The method of claim 5 , wherein the nanoparticle precursor is aluminum nitride (AIN), gallium nitride (GaN), tantalum nitride (TaN), tungsten nitride (W 2 N, WN, WN 2 ), magnesium nitride (Mg 3 N 2 ) or titanium nitride (TIN). 7. The method of claim 6 , wherein the nanoparticle precursor is AIN. 8. The method of claim 5 , wherein the nanoparticle precursor is copper metal, aluminum metal, silver metal, gold metal, gallium metal or magnesium metal. 9. The method of claim 8 , wherein the nanoparticle precursor is copper metal. 10. The method of claim 1 , wherein the source of boron is hexagonal boron nitride (h-BN); the source of nitrogen is a mixture of hexagonal boron nitride (h-BN) and N 2 ; and the source of hydrogen is H 2 . 11. The method of claim 10 , wherein the N 2 and H 2 are introduced into the stable induction plasma in a sheath gas. 12. The method of claim 11 , wherein the sheath gas further comprises argon. 13. The method of claim 10 , wherein the h-BN and the nanoparticle precursor are introduced into the stable induction plasma as a powder. 14. The method of claim 13 , wherein the ratio by weight of the h-BN to the nanoparticle precursor is from about 99:0.1 to about 50:50. 15. The method of claim 14 , wherein the ratio by weight of the h-BN to the nanoparticle precursor is from about 93.5:6.5 to about 50:50. 16. The method of claim 1 , wherein cooling the reaction mixture comprises cooling in a reaction zone downstream of the stable induction plasma.
Nanotubes · CPC title
obtained by TEM, STEM, STM or AFM · CPC title
by UV- or VIS- data · CPC title
by IR- or Raman-data · CPC title
After-treatment, e.g. grinding, purification (transformation of hexagonal into cubic or wurtzitic boron nitride C04B35/5831) · CPC title
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