IP Library Granted Patent US 7,879,306
Granted Patent B2
US 7,879,306 · App. 11/263,413 · Granted Feb 1, 2011

Dispersion and separation of nanostructured carbon in organic solvents

Assignee: Rochester Institute of Technology
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Quick Facts
Patent No.
US 7,879,306
App. No.
11/263,413
Granted
Feb 1, 2011
Kind
B2
Abstract

The present invention relates to dispersions of nanostructured carbon in organic solvents containing alkyl amide compounds and/or diamide compounds. The invention also relates to methods of dispersing nanostructured carbon in organic solvents and methods of mobilizing nanostructured carbon. Also disclosed are methods of determining the purity of nanostructured carbon.

Claims (72)

1. A dispersion of nanostructured carbon in an organic solvent, wherein the organic solvent comprises an alkyl amide compound having the structure:

wherein

R 1 and R 2 are independently selected from the group consisting of H, C 1 -C 6 alkyl, and phenyl, provided that R 1 and R 2 are not both H, and

R 3 is selected from the group consisting of C 1 -C 6 alkyl, phenyl, and

wherein

Z is N or CH;

R 4 , R 5 , R 6 , and R 7 are independently selected from the group consisting of H, C 1 -C 6 alkyl, and phenyl; and

n is an integer from 1 to 3.

2. The dispersion according to claim 1 , wherein R 1 , R 2 , and R 3 are independently selected from C 1 -C 6 alkyl and phenyl.

3. The dispersion according to claim 2 , wherein the alkyl amide compound is selected from the group consisting of N,N-dimethylacetamide, N,N-dimethylpropanamide, and N,N-diethylacetamide.

4. The dispersion according to claim 3 , wherein the alkyl amide compound is N,N-dimethylacetamide.

5. The dispersion according to claim 1 , wherein

R 3 is

R 1 , R 2 , R 4 , and R 5 are independently selected from C 1 -C 6 alkyl and phenyl.

6. The dispersion according to claim 5 , wherein

Z is N and

n is 1.

7. The dispersion according to claim 6 , wherein the alkyl amide compound is selected from the group consisting of N,N,N′,N′-tetramethylmalonamide, N,N′-dibutyl-N,N′-dimethylmalonamide, N,N,N′,N′-tetra(isopropyl)malonamide, N,N,N′,N′-tetrahexylmalonamide, 2-methyl-N,N,N′,N′-tetrahexylmalonamide, and N,N,N′,N′-tetrahexyl-2,2-dimethylmalonamide.

8. The dispersion according to claim 7 , wherein the alkyl amide compound is N,N,N′,N′-tetramethylmalonamide.

9. The dispersion according to claim 5 , wherein

Z is CH,

n is 1, and

R 4 and R 5 are H.

10. The dispersion according to claim 9 , wherein the alkyl amide compound is N,N-dimethylacetoacetamide.

11. The dispersion according to claim 5 , wherein

Z is N and

n is 2.

12. The dispersion according to claim 11 , wherein the alkyl amide compound is N,N,N′,N′-tetramethylsuccinamide.

13. The dispersion according to claim 1 , wherein the nanostructured carbon is selected from the group consisting of raw nanostructured carbon soot, purified nanostructured carbon, and mixtures thereof.

14. The dispersion according to claim 1 , wherein the nanostructured carbon is selected from the group consisting of carbon nanotubes, nano-onions, nano-horms, and fullerenes.

15. The dispersion according to claim 14 , wherein the nanostructured carbon comprises carbon nanotubes selected from the group consisting of single wall carbon nanotubes, double wall carbon nanotubes, and multi-wall carbon nanotubes.

16. The dispersion according to claim 15 , wherein the nanostructured carbon comprises single wall carbon nanotubes.

17. A method of mobilizing nanostructured carbon, said method comprising:

providing a dispersion of nanostructured carbon according to claim 1 and

applying an electrical field to the dispersion under conditions effective to mobilize the nanostructured carbon.

18. The method according to claim 17 , wherein the nanostructured carbon comprises single wall carbon nanotubes.

19. The method according to claim 17 further comprising:

depositing the nanostructured carbon onto a substrate.

20. The method according to claim 19 , wherein the substrate is selected from the group consisting of a metal electrode and a doped semiconductor.

21. A method of dispersing nanostructured carbon in an organic solvent, said method comprising:

providing nanostructured carbon and

contacting the nanostructured carbon with an organic solvent comprising an alkyl amide compound having the structure:

wherein

R 1 and R 2 , are independently selected from the group consisting of H, C 1 -C 6 alkyl, and phenyl, provided that R 1 and R 2 are not both H, and

R 3 is selected from the group consisting of H, C 1 -C 6 alkyl, phenyl and

wherein

Z is N or CH;

R 4 , R 5 , R 6 , and R 7 are independently selected from the group consisting of H, C 1 to C 6 alkyl, and phenyl; and

n is an integer from 1 to 3

under conditions effective to disperse the nanostructured carbon in the organic solvent.

22. The method according to claim 21 , wherein R 1 , R 2 , and R 3 are independently selected from C 1 -C 6 alkyl and phenyl.

23. The method according to claim 22 , wherein the alkyl amide compound is selected from the group consisting of N,N-dimethylacetamide, N,N-dimethylpropanamide, and N,N-diethylacetamide.

24. The method according to claim 23 , wherein the alkyl amide compound is N,N-dimethylacetamide.

25. The method according to claim 21 , wherein

R 3 is

R 1 , R 2 , R 4 , and R 5 are independently selected from C 1 -C 6 alkyl and phenyl.

26. The method according to claim 25 , wherein

Z is N and

n is 1.

27. The method according to claim 26 , wherein the alkyl amide compound is selected from the group consisting of N,N,N′,N′-tetramethylmalonamide, N,N′-dibutyl-N,N′-dimethylmalonamide, N,N,N′,N′-tetra(isopropyl)malonamide, N,N,N′,N′-tetrahexylmalonamide, 2-methyl-N,N,N′,N′-tetrahexylmalonamide, and N,N,N′,N′-tetrahexyl-2,2-dimethylmalonamide.

28. The method according to claim 27 , wherein the alkyl amide compound is N,N,N′,N′-tetramethylmalonamide.

29. The method according to claim 25 , wherein

Z is CH,

n is 1, and

R 4 and R 5 are H.

30. The method according to claim 29 , wherein the alkyl amide compound is N,N-dimethylacetoacetamide.

31. The method according to claim 25 , wherein n is 2.

32. The method according to claim 31 , wherein the alkyl amide compound is N,N,N′,N′-tetramethylsuccinamide.

33. The method according to claim 21 , wherein the nanostructured carbon is selected from the group consisting of raw nanostructured carbon soot, purified nanostructured carbon, and mixtures thereof.

34. The method according to claim 21 , wherein the nanostructured carbon is selected from the group consisting of carbon nanotubes, nano-onions, nano-horms, and fullerenes.

35. The method according to claim 34 , wherein the nanostructured carbon comprises carbon nanotubes selected from the group consisting of single wall carbon nanotubes, double wall carbon nanotubes, and multi-wall carbon nanotubes.

36. The method according to claim 35 , wherein the nanostructured carbon comprises single wall carbon nanotubes.

Assignments (2)
CONFIRMATORY LICENSE Recorded Jul 31, 2009
From: ROCHESTER INSTITUTE OF TECHNOLOGY
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 023042/0846 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2006
From: LANDI, BRIAN J.; RAFFAELLE, RYNE P.; RUF, HERBERT J.; EVANS CHRISTOPHER M.
To: ROCHESTER INSTITUTE OF TECHNOLOGY
Reel/Frame 017443/0954 →
Continuity (2)
Provisional Application 6062332200 · Oct 29, 2004
Related Publication 20080008643A1 · Jan 10, 2008