Modified boron nitride nanotubes and solutions thereof
A modified boron nitride nanotube (BNNT) comprising pendant hydroxyl (OH) and amino (NH 2 ) functional groups covalently bonded to a surface of the BNNT. Aqueous and organic solutions of these modified BNNTs are disclosed, along with methods of producing the same. The modified BNNTs and their solutions can be used to coat substrates and to make nanocomposites.
1. A modified boron nitride nanotube (BNNT) comprising pendant hydroxyl (OH) and pendant amino (NH 2 ) functional groups covalently bonded to a surface of the BNNT.
2. The modified BNNT of claim 1 , wherein the modified BNNT is single-walled, double-walled, few-walled, or multi-walled.
3. The modified BNNT of claim 1 , wherein a ratio of the pendant OH groups to pendant NH 2 groups is about 2:1.
4. The modified BNNT of claim 1 , wherein the number of pendant OH groups is between about 1 OH per 6 BN-units and about 1 OH per 240 BN-units.
5. An aqueous solution of modified boron nitride nanotubes (BNNTs) comprising modified BNNTs as defined in claim 1 , wherein the aqueous solution has a pH of between about 4 and about 8.
6. The aqueous solution of claim 5 , wherein the solubility of the modified BNNTs is about 1 mg/mL of solution, or less.
7. An organic solution of modified boron nitride nanotubes (BNNTs) comprising:
a) a polar organic solvent; and
b) modified BNNTs as defined in claim 1 .
8. The organic solution of claim 7 , wherein the polar organic solvent is an alkyl alcohol, acetonitrile, dimethylformamide (DMF), acetone or tetrahydrofuran (THF).
9. A method for producing an aqueous solution of modified boron nitride nanotubes (BNNTs), the aqueous solution having a pH of from about 4 to about 8, wherein:
the modified BNNTs are as defined in claim 1 ; and
the method comprises treating BNNTs with a halogen in an aqueous medium.
10. The method of claim 9 , further comprising adjusting the pH of the aqueous medium to between about 5 and about 7.
11. A method for producing an organic solution of modified boron nitride nanotubes (BNNTs), wherein:
the modified BNNTs are as defined in claim 1 ; and
the method comprises:
a) treating BNNTs with a halogen in an aqueous medium to provide an aqueous solution of the modified BNNTs;
b) adjusting a pH of the aqueous solution outside a range of about 4 to about 8 to precipitate at least a portion of the modified BNNTs
c) collecting the precipitate from step (b) comprising modified BNNTs; and
d) adding a polar organic solvent to the modified BNNTs to solubilize at least a portion of the modified BNNTs in the polar organic solvent.
12. A method of coating a surface of a substrate with modified boron nitride nanotubes (BNNTs), wherein the method comprises:
contacting the surface of the substrate with the aqueous solution of claim 5 ; and
evaporating the solvent of the aqueous solution from the surface of the substrate.
13. The method of claim 12 , wherein the substrate is a hydrophilic substrate.
14. The method of claim 12 , wherein the substrate is an optical glass fibre, a polyacrylate, a silicon wafer, a glass, a PC film, a PET film or a polyimide film.
15. A method of coating a surface of a substrate with modified boron nitride nanotubes (BNNTs), wherein the method comprises:
contacting the surface of the substrate with the organic solution of claim 7 ; and
evaporating the polar organic solvent of the organic solution from the surface of the substrate.
16. The method of claim 15 , wherein the substrate is a hydrophobic substrate.
17. The method of claim 15 , wherein the substrate is an optical glass fibre, a polyacrylate, a glass or a silicon wafer.
18. A nanocomposite comprising:
modified boron nitride nanotubes (BNNTs) as defined in claim 1 ; and
one or more of a polymer, a ceramic, a metal, an epoxy resin polymer, and an epoxy resin monomer.
19. A method for producing modified boron nitride nanotubes (BNNTs) comprising pendant hydroxyl (OH) and pendant amino (NH 2 ) functional groups covalently bonded to a surface of the BNNTs, the method comprising treating BNNTs with a halogen in an aqueous solution.
20. The method of claim 19 , wherein the treatment is carried out at a temperature of between about 20° C. and about 50° C. for a period of about 4 hours to about 48 hours.
21. The method of claim 19 , wherein the halogen is chlorine, bromine or iodine.
22. The method of claim 21 , wherein the halogen is bromine.