|Publication number||US20060008403 A1|
|Application number||US 11/173,419|
|Publication date||Jan 12, 2006|
|Filing date||Jul 1, 2005|
|Priority date||Jul 9, 2004|
|Also published as||EP1928785A2, EP1928785A4, US7815886, US20080050303, US20110033366, WO2008036065A2, WO2008036065A3|
|Publication number||11173419, 173419, US 2006/0008403 A1, US 2006/008403 A1, US 20060008403 A1, US 20060008403A1, US 2006008403 A1, US 2006008403A1, US-A1-20060008403, US-A1-2006008403, US2006/0008403A1, US2006/008403A1, US20060008403 A1, US20060008403A1, US2006008403 A1, US2006008403A1|
|Original Assignee||Clean Technologies International Corporation|
|Export Citation||BiBTeX, EndNote, RefMan|
|Patent Citations (47), Referenced by (14), Classifications (16), Legal Events (2)|
|External Links: USPTO, USPTO Assignment, Espacenet|
This application is a continuation-in-part of U.S. patent application Ser. No. 10/887,695, entitled “Method and Apparatus for Producing Carbon Nanostructures,” and a continuation-in-part of U.S. patent application Ser. No. 11/025,717, entitled “Method and Apparatus for Preparing A Collection Surface for Use in Producing Carbon Nanostructures.” The Applicant claims the benefit of each of these applications under 35 U.S.C. § 120. The entire content of each of these applications is incorporated herein by this reference.
The present invention relates to methods for manufacturing carbon nanotubes and other carbon nanostructures from a carbon-bearing feedstock. In particular, the invention relates to methods for placing carbon atoms in condition to form impurity-free carbon nanostructures. The invention also includes a particular type of carbon nanostructure.
Carbon nanostructures have received a great deal of interest since their discovery. It has been suggested that carbon nanostructures may have important applications in electronics, in materials sciences, and in a number of additional fields. As used in this disclosure, a carbon nanostructure comprises a structure formed from chemically bonded carbon atoms, with or without impurities or intentionally added materials incorporated in the carbon structure or adjacent to the carbon structure. Carbon nanostructures include structures in which carbon atoms are arranged in generally a series of interconnected hexagonal rings formed into a tube or other structure. Carbon nanostructures may be single walled or multiple walled nanotubes, nanofibers, nanorope, or nanowire. Single wall nanotubes include a single layer of the hexagonally arranged carbon atoms, while multiple walled nanotubes are made up of an inner layer of carbon atoms and a series of one or more outer layers of hexagonally arranged carbon atom structures.
Despite the interest in carbon nanostructures and the potentially important uses for such structures, the practical application of carbon nanostructures in products has been slowed by the difficulty in manufacturing such structures. Two general types of processes have been employed to produce or isolate carbon nanostructures. One process type uses a plasma arc between carbon electrodes. U.S. Pat. Nos. 5,482,601 and 5,753,088 describe such carbon plasma arc processes for producing carbon nanotubes. Another process type involves simply isolating naturally formed carbon nanotubes from graphite and soot. Such an isolation process or refinement process for carbon nanotubes is described in U.S. Pat. No. 5,560,898.
The prior processes for producing or isolating carbon nanotubes have been found to produce only small quantities of carbon nanotubes of inconsistent quality. The low quality carbon nanotubes produced or isolated by the prior methods commonly included metal or other atoms incorporated in the carbon structure. These impurities incorporated in the walls of the carbon nanotubes may have a negative impact on the qualities and properties of the nanotube and may render it unsuitable for an intended purpose. In particular, prior carbon nanostructure production techniques include no mechanism for preventing hydrogen atoms and other atoms that may be present in the carbon-bearing feed material from being incorporated into the nanocarbon structure. Also, prior carbon nanostructure production techniques tend to allow carbon from the feed material to become incorporated into the carbon nanostructures in an unpredictable fashion outside of the desired interconnected hexagonal ring structure. This inclusion of amorphous carbon in the resulting carbon nanostructure greatly degrades the properties and usefulness of the resulting carbon nanostructure.
The present invention provides methods for placing carbon in condition to form high-quality, substantially impurity-free carbon nanostructures. The present invention also encompasses a novel type of carbon nanostructure.
A method according to the present invention includes isolating carbon atoms as conditioned carbide anions below a surface of a reactant liquid. The conditioned carbide anions are then allowed to escape from the reactant liquid to a collection area where carbon nanostructures may form. The isolation of carbon atoms as conditioned carbide anions includes two components. A first component involves separating the carbon atoms from a carbon-bearing feed material that has been introduced into the reactant liquid and preventing the carbon atoms from combining with other materials. The second component of isolating carbon atoms as the desired conditioned carbide anions involves increasing the energy state of the separated and isolated carbon atoms. The desired energy state of carbide anions within the scope of the present claims is at least the SP3 hybrid energy state, in which the carbide anions have absorbed greater than 22 eV (electron volt) of energy from the reactant liquid bath. Thus, a “conditioned carbide anion” within the scope of the present claims refers to a carbide anion at least at the SP3 hybrid energy state.
The isolation of carbon atoms as conditioned carbide anions within the scope of the present invention may be accomplished by chemical reduction, chemical oxidation, reactions from acids, bases, or salts, or pyrolysis in the reactant liquid. For example, one preferred form of the invention utilizes a liquid reactant metal to chemically reduce a carbon-bearing feed material to isolate carbon atoms from the feed material and elevate the energy state of the isolated carbon atoms to form the desired conditioned carbon anions, that is, carbon anions at least at the SP3 hybrid energy state. Regardless of the particular mechanism by which the reactant liquid isolates the carbon atoms, maintaining carbon atoms that have been separated from the feed material below the surface of the reactant liquid allows the carbon atoms to remain isolated from each other and other materials with which bonds could form and allows the carbon atoms to be energized to the desired conditioned state.
A carbon structure according to the present invention includes at least one layer made up of hexagonally arranged carbon atoms. Each carbon atom has three covalent bonds to adjoining carbon atoms and one unbound pi electron. Thus, the carbon structure according to the present invention is a pure carbon structure, free of contaminating amorphous carbon and any other contaminating atoms. The carbon structure according to the invention is also free of hydrogen that would otherwise form a fourth covalent bond with each carbon atom. This contamination-free and hydrogen-free carbon structure may take the form of flat sheets of material or single or multi-walled tubes.
These and other advantages and features of the invention will be apparent from the following description of the preferred embodiments, considered along with the accompanying drawings.
The claims at the end of this application set out novel features which the Applicant believes are characteristic of the invention. The various advantages and features of the invention together with preferred modes of use of the invention will best be understood by reference to the following description of illustrative embodiments read in conjunction with the drawings introduced above.
Referring to the diagrammatic representation of
The apparatus shown in
The function of the tunnel structure defined by side walls 115 and upper wall 114 is to help ensure good contact between the reactant liquid and the feed material and between the reactant liquid and any intermediate reaction products that form from initial reactions of feed material, and to ensure sufficient residence time for the feed material and reaction products in the reactant liquid. This contact and residence time helps ensure the isolation of substantially all carbon from the carbon-bearing feed material and elevation of the resulting carbon anions to the desired conditioned carbon anions. The placement of the tunnel below the reactant liquid level 102 also ensures that a pressure is maintained on the feed material and intermediate reaction products. This pressure results from the column of reactant liquid above the feed material and intermediate reaction products. The tunnel structure shown in the present drawings includes one or more vents or passages 120 along the length of the tunnel structure to allow fresh reactant liquid to continually flow into the tunnel structure along its length and to help accommodate the expansion of gasses in the tunnel.
The form of the invention shown in
Feed material injection arrangement 103 includes an injection conduit 124 having an outlet end that extends to injection point 104 below the reactant liquid level 102. The injection point 104 is located so that the feed material exiting the conduit is captured within the tunnel structure under upper wall 114, and thus is forced to flow along the upper wall and along the entire length of the tunnel structure before it can exit the reactant liquid in effluent ejection area 108. This flow along the lower surface of upper tunnel wall 114 helps ensure complete destruction of the feed material and any intermediate reaction products that may form as the feed material is destroyed by reaction with or in the reactant liquid, and results in the formation of the desired isolated carbon anions in the reactant liquid. Injection point 104 is also preferably at a depth below the reactant liquid level 102 to produce a desired reaction pressure due to the column of reactant liquid above the injection point. For a predominantly aluminum reactant liquid, this pressure is approximately 2.4 pounds per square inch above atmospheric pressure. Due to the relatively high temperature that may be present in the reactant liquid, conduit 124 is preferably enclosed in a suitable thermal insulating sheath 127 which may comprise one or more layers of insulating material or a jacket through which a cooling fluid may be circulated. The upper end of conduit 124 is connected to a line which ultimately extends to a feed material supply 128 and preferably a purge gas supply 129 through a suitable arrangement of control valves 130.
Collection chamber 107 is located with respect to the outlet end 117 of the tunnel structure so that reaction products 118 are ultimately captured in the collection chamber. That is, the reaction products 118 flow up from flow channels 119 and traverse the surface of the reactant liquid in effluent ejection area 108 into the area defined as collection chamber 107. This area is defined by chamber walls 134. An outlet conduit 135 receives material that is not collected within chamber 107, and removes that material from the system. This material removed through conduit 135 may include gasses such as hydrogen and nitrogen, carbon, and particulates that escape the reactant liquid bath. Although it is not shown in
In the form of the invention shown in
Collection surface 110 may be located from just above reactant liquid level 102 (an inch or less) to as much as three feet above the reactant liquid. One or more seed objects may be included on collection surface 110. Seed objects may be any type of objects that encourage or facilitate the assembly of carbon nanostructures from the conditioned carbon atoms exiting the reactant liquid bath. Seed objects may include pure catalyst metals such as titanium and platinum, for example, or metal oxides such as manganese oxide, magnesium oxide, copper oxide, chromium oxide, and titanium oxide, for example. The catalyst may or may not be sacrificial. Seed objects may also include graphite surfaces, carbon surfaces, and seed carbon nanostructures. The seed objects may be spaced apart across collection surface 110 or may make up the entire collection surface. For example, the entire collection structure 138 may be formed from graphite or carbon or some other material that serves as a seed material. In another example, seed objects comprising atoms of catalyst metals may be liberated from reactant liquid 105 and deposited across collection surface 110 as described in related U.S. patent application Ser. No. 11/025,717.
The alternative embodiment shown in
The alternate collection arrangement shown in
A method according to the present invention may now be described with reference particularly to the embodiment shown in
The time and energy required to liberate carbon atoms from the carbon-bearing feed material will depend upon the nature of the feed material. For example, assuming a feed material of CH3, approximately 1735.5 Btu of kinetic energy per mole of feed material will be required to liberate the carbon atoms from the CH3 molecules. The energy required for this carbon liberation step may also be calculated for other carbon-bearing feed materials based on the bond energy required to break the chemical bonds to or between the carbon atoms in the respective feed material. Additional energy is then required to produce the desired conditioned carbon anions, that is, carbon anions at least at the SP3 hybrid energy state. Specifically, about 11 eV of kinetic energy is required to energize the carbon from the ground state to the first activation energy level, and about another 1.88 eV of energy is required to move the carbon (that is, the electrons associated with the carbon atom) from the first activation energy to the second activation energy level, which may be referred to as the 3PS2P2 energy state. From this point, additional energy in the amount of approximately 8 eV is required to move the electrons associated with the carbon atom from the second activation energy level to the 5S atomic structure of the SP3 hybrid energy state. Thus, once the chemical bonds of the feed stock are broken to isolate a carbon atom into the reactant liquid, the carbon then requires about 3.1703×10−21 Btus of energy per carbon atom, that is, about 25 electron volts of kinetic energy per atom, to be converted to the desired conditioned carbon anions. It will be noted that these conditioned carbon anions remain highly energetic while in the high energy conditions of the liquid reactant, and remain highly energetic and unstable at the time they escape from the high energy conditions of the liquid reactant material, such as by eluding into the collection chamber 107 shown in
To produce carbon nanostructure from the conditioned carbon anions generated in the reactant liquid, the conditioned carbon anions are allowed to traverse the surface of the reactant liquid in the effluent ejection area 108, and are directed across collection surface 110 which may include one or more seed materials or objects. Collection conditions are maintained in chamber 107 and at collection surface 110 at which the conditioned carbon anions phase change to a ground state by carbon nanostructure self-assembly.
Maintaining collection conditions in chamber 107 and at surface 110 may include controlling the temperature and effluent flow conditions as well as the appropriate atmosphere in chamber 107. In particular, an appropriate collection atmosphere comprises an atmosphere that does not chemically or physically interfere with the desired carbon nanostructure formation. Purging collection chamber 107 of materials that could chemically react with the conditioned carbon anions before they can form the desired nanocarbon structures may be particularly important in creating and maintaining the desired collection atmosphere. Thus, a preferred process includes first purging the chamber 107 by directing a suitable purge gas such as argon or some other noble gas or an inert gas from purge supply 129 to chamber 107. A separate purge arrangement may alternatively or additionally be included in the system with a purge inlet directly in chamber 107 to prevent having to run the purge gas through the reactant liquid.
The flow regime of effluent exiting the reactant liquid and flowing through collection chamber 107 may be important for allowing the conditioned carbon anions to bond together to produce the desired carbon nanostructures without extraneous atoms becoming incorporated in the structures. It is believed that a low velocity turbulent flow regime over collection surface 110 (that is, a flow producing eddy currents over the collection surface) best facilitates the production of carbon nanostructures without incorporating heavier atoms (such as metals) that may escape from the reactant liquid bath. It may also be possible to adjust the flow rate and composition of effluent flowing over collection surface in order to encourage the incorporation of various atoms other than carbon in the carbon nanostructures produced at the collection surface. The invention encompasses numerous techniques for controlling the composition and flow rate of effluent through collection chamber 107 and over collection surface 110. The relative amount of carbon-bearing feed material in the material injected at point 104 and the type or types of hydrocarbon materials injected may influence both flow rate and content of flow. An inert or noble gas may be injected together with the feed material from purge gas supply 129 or from some other supply to affect the flow rate of effluent through chamber 107 and the content of the effluent.
Some forms of the invention may purposefully inject one or more materials into the collection chamber 107 through a separate collection chamber input, that is, separate from effluent ejection area 108, in order to affect the flow characteristics in the flow chamber and in order to provide desired materials to be incorporated in the carbon nanostructures. Such a separate collection chamber input may include a suitable tube (not shown) which traverses a collection chamber wall and which includes an injection end at a point to direct injected materials against collection surface 110 and effluent flows up from the reactant liquid 105 and passes over the collection surface. Particles of seed material may also be injected into collection chamber 107 with such an injection conduit. These particles of seed material may be injected prior to enabling the conditioned carbon anions to flow across collection surface 110 or while conditioned carbon anions are flowing across the collection surface.
Numerous other variations may be employed to produce the desired flow regime and flow characteristics through collection chamber 107. Two methods are employed in apparatus 100 shown in
Any number of reactant liquids may be used to react the feed materials or feed material constituents according to the present invention. A preferred reactant liquid comprises liquid aluminum either alone or with other metals as disclosed in U.S. Pat. No. 5,000,101, which is also incorporated herein in its entirety. Temperatures may preferably range from approximately 650 degrees Celsius to approximately 950 degrees Celsius for reactant metals incorporating a substantial fraction of aluminum. Other reactant liquids may be used within different temperature ranges sufficient to liberate carbon atoms and place them in the desired chemically excited state as conditioned carbon anions for assembly into nanostructures at collection surface 110. The invention encompasses any liquid that either reacts with the feed material or otherwise causes carbon atoms to be liberated from the feed material and excited to conditioned carbon anions. The carbon atoms may be liberated by chemical reduction (as in the case of a reactant liquid made up predominantly of aluminum), by chemical oxidation, by providing chemically neutral electron reduction potentials, or by applying sufficient kinetic energy (through heat) to break the carbon bonds to other atoms in the feed molecules, or by any of these mechanisms. Liberated carbon atoms may then be converted to the desired conditioned carbon anions by any suitable process, preferably by heat applied through the reactant liquid. The reactant liquid may be a metal, acid, base, salt, or any combination of these. The temperature of the particular liquid will depend upon the particular reaction required to liberate carbon atoms from the feed material and the nature of the reactant liquid itself. For example, chemically neutral liquids that liberate carbon atoms by heat alone may be held at very high temperatures to produce the desired carbon liberation, and excitation to conditioned carbon anions. Temperatures on the order of approximately 1500 degrees Celsius or more may be required for carbon liberation and excitation by heat alone.
Collection surface 110 is also preferably maintained in a similar temperature range as the reactant liquid, and most preferably at a temperature just below the reactant liquid temperature, for example, approximately fifty (50) degrees Celsius or less below the liquid reactant temperature. Thus, the collection surface 110 and collection chamber 107 in areas near the collection surface will be isothermic or nearly isothermic with respect to the reactant liquid. It is believed that these reactant liquids, and temperatures, together with the reaction pressure and contact time with the reactant liquid not only liberate the carbon atoms from the hydrocarbon feed material but also places the liberated carbon in the excited state as conditioned carbon anions. The reactant liquid is also believed to surround the liberated carbon atoms while they are still in the reactant liquid to maintain the carbon atoms in the chemically excited state as conditioned carbon anions and prevent them from phase changing to a ground state before they have a chance to self-assemble into the desired nanostructures at the collection surface 110. The conditions are maintained at the collection surface according to the present invention so that these conditioned carbon anions phase change to a ground state as they bond covalently with other carbon atoms at the collection surface to form the desired carbon nanostructures.
It will be appreciated that some carbon that escapes the reactant liquid may also be diatomic carbon and double or triple bonded carbon. As used in this disclosure and the accompanying claims, “liberated carbon atoms” includes single atom carbon, diatomic carbon, and other two-carbon combinations such as two-carbon double bonded structures and two-carbon triple bonded structures. All of the liberated carbon atoms as well as all surviving carbon molecules escaping the reactant liquid will also be chemically excited, that is, will have active electrons. Some of the two-carbon combinations and/or other surviving carbon molecules that may escape the reactant liquid may be incorporated, together with single, chemically excited carbon atoms, into molecularly combined carbon nanostructures within the scope of the present invention.
The present invention may use any number of carbon-bearing compounds as the feed material or as part of the feed material. Preferred forms of the invention utilize hydrocarbon compounds including single-bonded carbon either predominantly or exclusively. However, compounds including double and triple bonded carbon may be used according to the invention provided sufficient contact time with the reactant liquid to liberate carbon atoms and energize them to conditioned carbon anions for assembly into carbon nanostructures, or to produce chemically excited carbon molecules for assembly into carbon nanostructures. Some forms of the invention may adjust the content of the various carbon-bearing materials in a feed material mixture to provide a desired concentration of liberated single carbon atoms and liberated carbon molecules for incorporation into the desired carbon nanostructures. For example, the feed materials may be manipulated so that the effluent escaping the reactant liquid includes carbon in desired relative concentrations of single carbon atoms and double bonded carbon molecules.
It is also noted that some reactant liquids are capable of liberating carbon atoms from highly stable forms of carbon. For example, the preferred reactant liquid made up of aluminum or alloys of aluminum has the capability of liberating carbon atoms from even highly stable forms of carbon such as graphite and carbon nanostructures given sufficient contact time. Thus, some types of reactant liquids, whether they operate by chemical reduction, chemical oxidation, pyrolysis, or by reactions from acids, bases, or salts, may be used to destroy carbon nanostructures and recycle the carbon atoms from these materials in different types of carbon materials. In one aspect of the present invention, carbon nanostructure materials may be introduced into a reactant liquid such as liquid aluminum or liquid aluminum alloy at 650 to 950 degrees Celsius to isolate conditioned carbon anions from the carbon nanostructure material. The conditioned carbon anions may then be directed to a recovery area where the liberated carbon may be recovered. The recovery area may comprise a collection chamber such as chamber 107 in
Tests which were conducted according to the present invention may be described with reference to the test apparatus 600 shown diagrammatically in
In the tests, once the injection conduit/collection structure was in place in vessel 601, argon gas was injected through input line 612 and ultimately through conduit 604 and the reactant metal to displace air and any other gasses trapped in the area between level 607 and top 605 which formed the collection area of the apparatus. Once the collection area was purged with argon gas, methane was injected through input 614 at a rate of approximately four liters per minute for between thirty and forty-eight hours. Thereafter, acetylene gas and motor oil were also pumped through conduit 604. The injection conduit/collection structure was then removed from vessel 601 and allowed to cool in open air. Black soot-like material was observed over substantially the entire upper surface of collection plate 610. This material was scraped off plate 610 in several areas and observed through a scanning electron microscope down to a resolution of approximately one micron and a transmission electron microscope at up to 200,000 times magnification. These observations showed single-walled carbon nanotubes, double-walled carbon nanotubes, nanofibers, and carbon nanoropes in the sample material.
It is believed that the hydrogen-free and impurity-free carbon nanostructures illustrated in
The above described preferred embodiments are intended to illustrate the principles of the invention, but not to limit the scope of the invention. Various other embodiments and modifications to these preferred embodiments may be made by those skilled in the art without departing from the scope of the present invention.
|Cited Patent||Filing date||Publication date||Applicant||Title|
|US500101 *||Dec 12, 1892||Jun 20, 1893||Charles w||Benjamin f|
|US3066099 *||Jun 29, 1959||Nov 27, 1962||Nilok Chemicals Inc||Mineral active carbon and process for producing same|
|US4357234 *||May 18, 1981||Nov 2, 1982||Canadian Patents & Development Limited||Alternating potential electrostatic separator of particles with different physical properties|
|US4663230 *||Dec 6, 1984||May 5, 1987||Hyperion Catalysis International, Inc.||Carbon fibrils, method for producing same and compositions containing same|
|US5000101 *||May 16, 1990||Mar 19, 1991||Wagner Anthony S||Hazardous waste reclamation process|
|US5094906 *||Apr 12, 1990||Mar 10, 1992||Exxon Research And Engineering Company||Ceramic microtubular materials and method of making same|
|US5167919 *||Mar 15, 1990||Dec 1, 1992||Wagner Anthony S||Waste treatment and metal reactant alloy composition|
|US5271341 *||Nov 27, 1992||Dec 21, 1993||Wagner Anthony S||Equipment and process for medical waste disintegration and reclamation|
|US5346683 *||Mar 26, 1993||Sep 13, 1994||Gas Research Institute||Uncapped and thinned carbon nanotubes and process|
|US5359947 *||Aug 9, 1993||Nov 1, 1994||Wagner Anthony S||Equipment and process for waste pyrolysis and off gas oxidative treatment|
|US5424054 *||May 21, 1993||Jun 13, 1995||International Business Machines Corporation||Carbon fibers and method for their production|
|US5431113 *||Oct 18, 1994||Jul 11, 1995||Wagner; Anthony S.||Equipment and process for molten alloy treatment of hazardous liquids and slurries|
|US5452671 *||Oct 7, 1994||Sep 26, 1995||Wagner; Anthony S.||Equipment and process for ultra hazardous liquid and gas molecular decomposition|
|US5457343 *||Dec 21, 1993||Oct 10, 1995||Nec Corporation||Carbon nanotubule enclosing a foreign material|
|US5461991 *||Apr 11, 1994||Oct 31, 1995||Wagner; Anthony S.||Equipment and process for molten alloy pyrolysis of hazardous liquid waste|
|US5482601 *||Jan 13, 1995||Jan 9, 1996||Director-General Of Agency Of Industrial Science And Technology||Method and device for the production of carbon nanotubes|
|US5489477 *||Mar 16, 1994||Feb 6, 1996||Nec Corporation||High-molecular weight carbon material and method of forming the same|
|US5553558 *||Apr 1, 1994||Sep 10, 1996||Wagner; Anthony S.||Equipment and process for surface treatment of hazardous solids and slurries with molten alloy|
|US5560898 *||Aug 1, 1994||Oct 1, 1996||Director-General Of Agency Of Industrial Science And Technology||Process of isolating carbon nanotubes from a mixture containing carbon nanotubes and graphite particles|
|US5564351 *||Oct 3, 1994||Oct 15, 1996||Wagner; Anthony S.||Equipment and process for molecular decomposition of chlorinated hydrocarbons|
|US5640702 *||Sep 1, 1994||Jun 17, 1997||Shultz; Clifford G.||Method of and system for treating mixed radioactive and hazardous wastes|
|US5641466 *||Jun 2, 1994||Jun 24, 1997||Nec Corporation||Method of purifying carbon nanotubes|
|US5695734 *||Sep 15, 1995||Dec 9, 1997||Director-General Of Agency Of Industrial Science & Technology||Process for the separation of carbon nanotubes from graphite|
|US5698175 *||Jul 3, 1995||Dec 16, 1997||Nec Corporation||Process for purifying, uncapping and chemically modifying carbon nanotubes|
|US5753088 *||Feb 18, 1997||May 19, 1998||General Motors Corporation||Method for making carbon nanotubes|
|US5832845 *||Oct 15, 1996||Nov 10, 1998||Wagner; Anthony S.||Equipment for molecular decomposition of hazardous wastes using a molten media reactor|
|US6037517 *||Nov 4, 1998||Mar 14, 2000||Clean Technologies International Corporation||Apparatus and method for treating waste materials which include charged particle emitters|
|US6069290 *||Jun 1, 1998||May 30, 2000||Clean Technologies International Corporation||Waste treatment process and reactant metal alloy|
|US6195382 *||Mar 23, 1999||Feb 27, 2001||Clean Technologies International Corporation||High temperature molten metal reactor and waste treatment method|
|US6227126 *||Jan 15, 1999||May 8, 2001||Clean Technologies, International Corporation||Molten metal reactor and treatment method for treating gaseous materials and materials which include volatile components|
|US6256466 *||Mar 9, 2000||Jul 3, 2001||Kyocera Mita Corporation||Developing device capable of preventing toner particles from being accumulated at a front end of a cover member|
|US6270735 *||Aug 18, 1998||Aug 7, 2001||Clean Technologies International Corporation||Apparatus for thermal stripping and molecular decomposition for waste streams|
|US6303094 *||Mar 23, 1998||Oct 16, 2001||Japan Fine Ceramics Center||Process for producing carbon nanotubes, process for producing carbon nanotube film, and structure provided with carbon nanotube film|
|US6333016 *||Sep 3, 1999||Dec 25, 2001||The Board Of Regents Of The University Of Oklahoma||Method of producing carbon nanotubes|
|US6346221 *||Sep 17, 1998||Feb 12, 2002||Clean Technologies International Corporation||Apparatus for recovering materials from waste tires|
|US6451175 *||Aug 15, 2000||Sep 17, 2002||Wisconsin Alumni Research Foundation||Method and apparatus for carbon nanotube production|
|US6455021 *||Jul 20, 1999||Sep 24, 2002||Showa Denko K.K.||Method for producing carbon nanotubes|
|US6683783 *||Mar 6, 1998||Jan 27, 2004||William Marsh Rice University||Carbon fibers formed from single-wall carbon nanotubes|
|US6717026 *||Dec 11, 2001||Apr 6, 2004||Clean Technologies International Corporation||Molten metal reactor utilizing molten metal flow for feed material and reaction product entrapment|
|US6740224 *||Jun 11, 2002||May 25, 2004||The United States Of America As Represented By The Administrator Of The National Aeronautics And Space Administration||Method of manufacturing carbon nanotubes|
|US6740403 *||Apr 2, 2001||May 25, 2004||Toyo Tanso Co., Ltd.||Graphitic polyhederal crystals in the form of nanotubes, whiskers and nanorods, methods for their production and uses thereof|
|US6761871 *||May 22, 2001||Jul 13, 2004||Reginald Bernard Little||Magnetic production of carbon nanotubes and filaments|
|US6765949 *||Aug 29, 2002||Jul 20, 2004||Robert P. H. Chang||Carbon nanostructures and methods of preparation|
|US6841003 *||Nov 22, 2002||Jan 11, 2005||Cdream Display Corporation||Method for forming carbon nanotubes with intermediate purification steps|
|US6843850 *||Aug 23, 2002||Jan 18, 2005||International Business Machines Corporation||Catalyst-free growth of single-wall carbon nanotubes|
|US20020102193 *||Jan 29, 2002||Aug 1, 2002||William Marsh Rice University||Process utilizing two zones for making single-wall carbon nanotubes|
|US20030129119 *||May 24, 2002||Jul 10, 2003||Hsin-Tien Chiu||Nanocarbon materials and process for producing the same|
|Citing Patent||Filing date||Publication date||Applicant||Title|
|US7550128||Jul 9, 2004||Jun 23, 2009||Clean Technologies International Corporation||Method and apparatus for producing carbon nanostructures|
|US7563426||Dec 29, 2004||Jul 21, 2009||Clean Technologies International Corporation||Method and apparatus for preparing a collection surface for use in producing carbon nanostructures|
|US7587985||Aug 16, 2004||Sep 15, 2009||Clean Technology International Corporation||Method and apparatus for producing fine carbon particles|
|US7814846||Oct 31, 2007||Oct 19, 2010||Clean Technology International Corporation||Method and apparatus for preparing a collection area for use in producing carbon nanostructures|
|US7815885||Oct 31, 2007||Oct 19, 2010||Clean Technology International Corporation||Method and apparatus for producing carbon nanostructures|
|US7815886||Oct 31, 2007||Oct 19, 2010||Clean Technology International Corporation||Reactant liquid system for facilitating the production of carbon nanostructures|
|US7901653||Oct 31, 2007||Mar 8, 2011||Clean Technology International Corporation||Spherical carbon nanostructure and method for producing spherical carbon nanostructures|
|US7922993||May 9, 2006||Apr 12, 2011||Clean Technology International Corporation||Spherical carbon nanostructure and method for producing spherical carbon nanostructures|
|US8197787||Sep 14, 2009||Jun 12, 2012||Clean Technology International Corporation||Method and apparatus for producing fine carbon particles|
|US8263037||Apr 11, 2011||Sep 11, 2012||Clean Technology International Corporation||Spherical carbon nanostructure and method for producing spherical carbon nanostructures|
|US8299014||Dec 5, 2011||Oct 30, 2012||Clean Technology International Corporation||Material for facilitating thermal treatments of biological tissues and method of energy targeting leading to thermal treatment of biological tissues|
|US20060008405 *||Jul 9, 2004||Jan 12, 2006||Wagner Anthony S||Method and apparatus for producing carbon nanostructures|
|US20060008406 *||Dec 29, 2004||Jan 12, 2006||Clean Technologies International Corporation||Method and apparatus for preparing a collection surface for use in producing carbon nanostructures|
|US20060034746 *||Aug 16, 2004||Feb 16, 2006||Wagner Anthony S||Method and apparatus for producing fine carbon particles|
|Cooperative Classification||Y10S977/842, Y10S977/844, C01B31/0246, C01B31/0293, B82Y40/00, C01B2202/04, B82Y30/00, C01B2202/02, C01B31/30|
|European Classification||B82Y30/00, C01B31/02B4B6, C01B31/02B6, B82Y40/00, C01B31/30|
|Jul 1, 2005||AS||Assignment|
Owner name: CLEAN TECHNOLOGIES INTERNATIONAL CORPORATION, TEXA
Free format text: ASSIGNMENT OF ASSIGNORS INTEREST;ASSIGNOR:WAGNER, ANTHONY S.;REEL/FRAME:016721/0377
Effective date: 20050630
|Oct 15, 2009||AS||Assignment|
Owner name: CLEAN TECHNOLOGY INTERNATIONAL CORPORATION, TEXAS
Free format text: CORRECTIVE ASSIGNMENT TO CORRECT THE NAME OF THE ASSIGNEE SHOWN IN THE ORIGINAL ASSIGNMENT PREVIOUSLY RECORDED ON REEL 016721 FRAME 0377;ASSIGNOR:WAGNER, ANTHONY S.;REEL/FRAME:023374/0867
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