IP Library Granted Patent US 9,394,174
Granted Patent B2
US 9,394,174 · App. 13/975,745 · Granted Jul 19, 2016

Alkyne-assisted nanostructure growth

Inventors: Desiree L. Plata (Holyoke, MA); Philip M. Gschwend (Lexington, MA); Anastasios John Hart (Cambridge, MA); Eric R. Meshot (Ann Arbor, MI); Christopher M. Reddy (Falmouth, MA)
Assignees: Massachusetts Institute of Technology; Woods Hole Oceanographic Institute; The Regents of the University of Michigan
C01B31/0226B82Y30/00B82Y40/00C01B31/0293
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Quick Facts
Patent No.
US 9,394,174
App. No.
13/975,745
Granted
Jul 19, 2016
Kind
B2
Abstract

The present invention relates to the formation and processing of nanostructures including nanotubes. Some embodiments provide processes for nanostructure growth using relatively mild conditions (e.g., low temperatures). In some cases, methods of the invention may improve the efficiency (e.g., catalyst efficiency) of nanostructure formation and may reduce the production of undesired byproducts during nanostructure formation, including volatile organic compounds and/or polycylic aromatic hydrocarbons. Such methods can both reduce the costs associated with nanostructure formation, as well as reduce the harmful effects of nanostructure fabrication on environmental and public health and safety.

Claims (27)

1. A method for forming carbon nanostructures, comprising:

providing a reactant vapor having a temperature of less than 300° C.;

maintaining the reactant vapor at a temperature of less than 300° C.; and

contacting the reactant vapor with a catalyst material to cause formation of nanostructures,

wherein the reactant vapor comprises an alkyne and an alkene,

wherein the catalyst material is positioned within a reaction chamber having a temperature of less than 70° C.

2. A method as in claim 1 , wherein the alkyne is ethyne, propyne, but-1-en-3-yne, or 1,3-butadiyne.

3. A method as in claim 1 , wherein the reactant vapor comprises ethylene, hydrogen, and an alkyne.

4. A method as in claim 1 , wherein the reactant vapor comprises, by volume, 16% to 35% ethylene, 16% to 70% hydrogen, and 0.1% or less alkyne, such that the total amount of ethylene, hydrogen, and alkyne equals 100%.

5. A method as in claim 1 , wherein the reactant vapor comprises, by volume, 20% ethylene, 51% hydrogen, and 29% helium.

6. A method as in claim 1 , wherein the reactant gas is substantially free of an oxygen-containing species, provided that the oxygen-containing species is not water.

7. A method as in claim 1 , wherein the act of contacting causes formation of a product vapor comprising at least one carbon-containing byproduct.

8. A method as in claim 1 , wherein the reactant vapor is maintained at a temperature of less than 100° C. prior to contacting the catalyst material.

9. A method as in claim 1 , wherein the reactant vapor is maintained at a temperature of less than 50° C. prior to contacting the catalyst material.

10. A method as in claim 1 , wherein the reactant vapor is maintained at a temperature of less than 25° C. prior to contacting the catalyst material.

11. A method as in claim 1 , wherein the nanostructures are formed on a surface of the catalyst material.

12. A method as in claim 1 , wherein the nanostructures are single-walled carbon nanotubes or multi-walled carbon nanotubes.

13. A method as in claim 1 , wherein the nanostructures are vertically aligned multi-walled carbon nanotubes.

14. A method as in claim 1 , wherein the catalyst material comprises iron.

15. A method as in claim 1 , wherein the act of contacting causes formation of a product vapor comprising at least one volatile organic compound (VOC) or polycyclic aromatic hydrocarbon (PAH).

16. A method as in claim 15 , wherein the volatile organic compound is methane, ethane, propane, propene, 1,2-butadiene, 1,3-butadiene, 1,3-butadiyne, pentane, pentene, cyclopentadiene, hexene, or benzene.

17. A method as in claim 15 , wherein the polycyclic aromatic hydrocarbon is naphthalene, acenaphthalene, fluorene, phenanthrene, anthracene, fluoranthene, pyrene, chrysene, coronene, triphenylene, naphthacene, phenanthrelene, picene, fluorene, perylene, or benzopyrene.

18. A method as in claim 16 , wherein the product vapor comprises methane in an amount less than 0.4% of the total volume of product vapor that exits the reaction chamber during formation of the nanostructure, and wherein methane is substantially not present in the reactant vapor.

19. A method as in claim 16 , wherein the product vapor comprises 1,3-butadiene in an amount less than 0.4% of the total volume of product vapor that exits the reaction chamber during formation of the nanostructure, and wherein 1,3-butadiene is substantially not present in the reactant vapor.

20. A method as in claim 17 , wherein the product vapor comprises benzene in an amount less than 0.3% of the total volume of product vapor that exits the reaction chamber during formation of the nanostructure, and wherein benzene is substantially not present in the reactant vapor.

21. A method as in claim 1 , wherein the nanostructures are formed at a growth rate of at least 1 micron per second.

22. A method as in claim 1 , wherein the nanostructures are formed with a catalyst efficiency of about 1×10 2 grams of nanostructure/grams of catalyst material or greater.

Assignments (5)
CONFIRMATORY LICENSE Recorded Jun 25, 2014
From: UNIVERSITY OF MICHIGAN
To: NATIONAL SCIENCE FOUNDATION
Reel/Frame 033227/0897 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2014
From: HART, ANASTASIOS JOHN; MESHOT, ERIC R.
To: UNIVERSITY OF MICHIGAN, THE BOARD OF REGENTS ACTING FOR AND ON BEHALF OF THE C/O TECHNOLOGY MANAGEMENT OFFICE
Reel/Frame 032774/0072 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2014
From: PLATA, DESIREE L.
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY; WOODS HOLE OCEANOGRAPHIC INSTITUTE
Reel/Frame 032774/0275 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2014
From: GSCHWEND, PHILIP M.
To: MASSACHUSETTS INSTITUTE OF TECHNOLOGY
Reel/Frame 032774/0416 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Apr 29, 2014
From: REDDY, CHRISTOPHER M.
To: WOODS HOLE OCEANOGRAPHIC INSTITUTE
Reel/Frame 032774/0520 →
Continuity (3)
Continuation 12817818 · Jun 17, 2010
Provisional Application 61187704 · Jun 17, 2009
Related Publication 20140134093A1 · May 15, 2014