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This invention relates generally to a method for growing carbon fiber from single-wall carbon nanotube (SWNT) molecular arrays. In one embodiment, the present invention involves a macroscopic molecular array of at least about 106tubular carbon molecules in generally parallel orientation and having s

This invention relates generally to a method for growing carbon fiber from single-wall carbon nanotube (SWNT) molecular arrays. In one embodiment, the present invention involves a macroscopic molecular array of at least about 106tubular carbon molecules in generally parallel orientation and having substantially similar lengths in the range of from about 50 to about 500 nanometers. The hemispheric fullerene cap is removed from the upper ends of the tubular carbon molecules in the array. The upper ends of the tubular carbon molecules in the array are then contacted with a catalytic metal. A gaseous source of carbon is supplied to the end of the array while localized energy is applied to the end of the array in order to heat the end to a temperature in the range of about 500° C. to about 1300° C. The growing carbon fiber is continuously recovered.

대표청구항 ▼

1. A method for continuously growing macroscopic carbon fiber comprising at least about 10 6single-wall nanotubes in generally parallel orientation, said method comprising the steps of: (a) providing a macroscopic molecular array of at least about 10 6tubular carbon molecules in generally parallel

1. A method for continuously growing macroscopic carbon fiber comprising at least about 10 6single-wall nanotubes in generally parallel orientation, said method comprising the steps of: (a) providing a macroscopic molecular array of at least about 10 6tubular carbon molecules in generally parallel orientation and having substantially similar lengths in the range of from about 50 to about 500 nanometers; (b) removing an end cap from an end of the tubular carbon molecules in said array to form a plurality of open ends of the tubular carbon molecules; (c) contacting the open ends of the tubular carbon molecules in said array with at least one catalytic metal; (d) supplying a gaseous source of carbon to the open ends of the tubular carbon molecules of said array while applying localized energy to the open ends of the tubular carbon molecules of said array to heat said open ends to a temperature in the range of about 500° C. to about 1300° C.; and (e) continuously recovering the growing carbon fiber. 2. The method of claim 1 wherein said fullerene caps are removed by heating in an oxidative environment.3. The method of claim 2, wherein said oxidative environment comprises aqueous etching with nitric acid.4. The method of claim 1 wherein said catalytic metal is selected from the group consisting of Group VIII transition metals, Group VI transition metals, metals of the lanthanide series, metals of the actinide series, and mixtures thereof.5. The method of claim 4 wherein said catalytic metal is selected from the group consisting of Fe, Co, Ni, Ru, Rh, Pd, Os, Ir and Pt.6. The method of claim 5 wherein said catalytic metal is selected from the group consisting of Fe, Ni, and Co, and mixtures thereof.7. The method of claim 4 wherein said catalytic metal is selected from the group consisting of Cr, Mo, and W.8. The method of claim 1 wherein said catalytic metal is deposited in situ on each nanotube as a metal atom cluster.9. The method of claim 8 wherein said metal atom cluster has from about 10 to about 200 metal atoms.10. The method of claim 1 wherein said catalytic metal is deposited as preformed nanoparticles.11. The method of claim 10 wherein said catalytic metal is Mo.12. The mod of claim 1 wherein said catalytic metal is deposited in the form of a metal precursor selected from the group consisting of salts, oxides and complexes of said metal.13. The method of claim 1 wherein said catalytic metal is deposited by evaporating metal atoms and allowing them to condense and coalesce on said open ends of the tubular carbon molecules.14. The method of claim 13 wherein said evaporating is done by heating at least one wire comprising said catalytic metal.15. The method of claim 13 wherein said evaporating is done by molecular beam evaporation.16. The method of claim 1 wherein the gaseous source of carbon is selected from the group consisting of hydrocarbons and carbon monoxide.17. The method of claim 1 wherein said hydrocarbon is a chemical selected from the group consisting methane, ethane, ethylene, acetylene, acetone, propane, propylene and mixtures thereof.18. The method of claim 1 wherein the gaseous source of carbon is selected from the group consisting of hydrocarbons and carbon monoxide.19. The method of claim 1 wherein said localized energy is provided by a laser beam.20. The method of claim 1 wherein said localized energy is provided by a source selected from the group consisting of a microwave generator, an R-F coil and a solar concentrator.21. The method of claim 1 wherein said open end is heated to a temperature in the range of about 900° C. to about 1100° C.22. The method of claim 2 wherein said oxidative environment comprises gas phase etching at temperatures of about 500° C. in an atmosphere of oxygen and CO2.23. A method for growing continuous carbon fiber comprising: a) providing an array of single-wall carbon nanotubes in generally parallel orientation; b) removing end caps from at least some of t he ends of the single-wall carbon nanotubes; c) contacting the ends of the single-wall carbon nanotubes with at least one catalytic metal, wherein the catalytic metal comprises a Group VI metal; d) activating the catalytic metal; e) adding a gaseous source of carbon to the array and catalytic metal; f) heating at least one of the array, the catalytic metal and the gaseous source of carbon; g) growing the single-wall carbon nanotubes at the ends of the single-wall carbon nanotubes to form a continuous carbon fiber, wherein the fiber comprises the single-wall carbon nanotubes in generally parallel orientation; and h) recovering the continuous carbon fiber. 24. The method of claim 23 wherein the catalytic metal is selected from the group consisting of chromium (Cr), molybdenum (Mo), tungsten (W) and mixtures thereof.25. The method of claim 23 wherein the gaseous source of carbon is selected from the group consisting of hydrocarbons and carbon monoxide.26. The method of claim 25 wherein the gaseous source of carbon is introduced at a partial pressure between 0.001 Torr and 1000 Torr.27. A method for growing continuous carbon fiber comprising: a) providing an array of single-wall carbon nanotubes in generally parallel orientation, wherein the array comprises at least 10 6of the single-wall carbon nanotubes; b) removing end caps from at least some of the ends of single-wall nanotubes; c) contacting the ends of the single-wall carbon nanotubes with at least one catalytic metal; d) activating the catalytic metal; e) adding a gaseous source of carbon to the array and catalytic metal; f) heating at least one of the array, the catalytic metal and the gaseous source of carbon; g) growing the single-wall carbon nanotubes at the ends of the single-wall carbon nanotubes to form a continuous carbon fiber, wherein the fiber comprises the single-wall carbon nanotubes in generally parallel orientation; and h) recovering the continuous carbon fiber. 28. A method for growing continuous carbon fiber comprising: a) providing an array of single-wall carbon nanotubes in generally parallel orientation, wherein the array comprises a plurality of single-wall carbon nanotubes having substantially similar lengths in the range from the about 50 to about 500 nm; b) removing end caps from at least some of the ends of single-wall nanotubes; c) contacting the ends of the single-wall carbon nanotubes with at least one catalytic metal; d) activating the catalytic metal; e) adding a gaseous source of carbon to the array and catalytic metal; f) heating at least one of the array, the catalytic metal and the gaseous source of carbon; g) growing the single-wall carbon nanotubes at the ends of the single-wall carbon nanotubes to form a continuous carbon fiber, wherein the fiber comprises the single-wall carbon nanotubes in generally parallel orientation; and h) recovering the continuous carbon fiber.