Abstract: By a method that includes coking a residue resulting from distillation of crude oil under reduced pressure and having API gravity of 1 to 5, an asphaltene content of 10 to 50%, a resin content of 5 to 30%, and a sulfur content of 1 to 12% to obtain coke, pulverizing the coke to obtain a carbon powder, and heating the carbon powder at 1000 to 3500 deg C., a graphite anode active material for use in a lithium secondary battery is obtained that has, in X-ray powder diffraction, d002 of not smaller than 0.3354 nm and not greater than 0.337 nm, Lc(004) of smaller than 100 nm, La(110) of not smaller than 100 nm, and a half width of the peak of a plane (101) at a diffraction angle (2?) of 44 degrees to 45 degrees of not smaller than 0.65 degree.

Abstract: An object of the present invention is to provide a graphite film, and a graphite composite film both having an excellent thermal diffusivity which can sufficiently manage heat dissipation of electronic instruments, precision instruments and the like, along with an excellent flex resistance which can withstand application to bent portions. Means for Resolution of the present invention is a graphite film exhibiting the number of reciprocal foldings being 10,000 times or more as measured using a rectangular strip test piece having a width of 15 mm until the test piece breaks in a MIT folding endurance test under conditions of: a curvature radius R of the bending clamp being 2 mm; a left-and-right bending angle being 135°; a bending rate being 90 times/min; and a load being 0.98 N.

Abstract: The present invention generally relates to methods and systems relating to the selection of substrates comprising crystalline templates for the controlled crystallization of molecular species. In some embodiments, the methods and systems allow for the controlled crystallization of a molecular species in a selected polymorphic form. In some embodiments, the molecular species is a small organic molecule (e.g., pharmaceutically active agent).

Abstract: Provided is a stock oil composition for a carbonaceous material for a negative electrode of a lithium-ion secondary battery which composition is useful for achieving excellent high-speed charge and discharge characteristics. The stock oil composition for a carbonaceous material for a negative electrode of a lithium-ion secondary battery uses a bottom oil of residue fluid catalytic cracking apparatus as a raw material. The stock oil composition comprises, of a saturated component, an aromatic component, a resin component and an asphaltene component detectable by development of the stock oil composition using thin-layer chromatography, the saturated component ranging from 30 to 50% by weight and the aromatic component ranging from 50 to 70% by weight; and has an average molecular weight of from 400 to 600.

Abstract: Methods of producing layers of patterned graphene with smooth edges are provided. The methods comprise the steps of fabricating a layer of crystalline graphene on a surface, wherein the layer of crystalline graphene has a crystallographically disordered edge, and decreasing the crystallographic disorder of the edge of the layer of crystalline graphene by heating the layer of crystalline graphene on the surface at an elevated temperature in a catalytic environment comprising carbon-containing molecules.

Abstract: Disclosed is a method for producing graphene functionalized at its edge positions of graphite. Organic material having one or more functional groups is reacted with graphite in reaction medium comprising methanesulfonic acid and phosphorus pentoxide, or in reaction medium comprising trifluoromethanesulfonic acid, to produce graphene having organic material fuctionalized at edges. And then, high purity and large scaled graphene and film can be obtained by dispersing, centrifugal separating the functionalized graphene in a solvent and reducing, in particular heat treating the graphene. According to the present invention graphene can be produced inexpensively in a large amount with a minimum loss of graphite.

Abstract: Provided are a method of manufacturing graphene, graphene manufactured by the method, a conductive thin film including the graphene, a transparent electrode comprising the graphene, and a radiating or heating device comprising the graphene. The method includes: preparing a graphene member including a base member, a hydrophilic oxide layer formed on the base member, a hydrophobic metal catalyst layer formed on the oxide layer, and graphene grown on the metal catalyst layer; applying water to the graphene member; separating the metal catalyst layer from the oxide layer; and removing the metal catalyst layer using an etching process.

Abstract: A low-temperature process for preparing flat carbon based nanostructured material, and namely foliated, fine graphite particles having low thickness and high aspect ratio. The process comprises the steps of: subjecting a particulate graphite to a mechanical attrition treatment in the presence of an alkaline reactant or a mixture comprising the alkaline reactant; exposing the graphite particles to an intercalating solvent to cause the solvent to penetrate between carbon layers of graphite; and delivering an ultrasonic energy into a dispersion of the graphite particles for a period of time sufficient to cause the formation of the nanostructured material. The carbon based nanostructures (CBNS) obtained by this method have a thickness in the range of 4-20 nm and an aspect ratio 500-7000 and various surface chemistry, and can be used as a highly functional graphite material in a wide range of applications, in particular for electrochemical applications in batteries and fuel cells.

Abstract: There is provided a method for forming a graphene layer. The method includes forming an article that comprises a carbon-containing self-assembled monolayer (SAM). A layer of nickel is deposited on the SAM. The article is heated in a reducing atmosphere and coolded. The heating and cooling steps are carried out so as to convert the SAM to a graphene layer.

Abstract: Methods of forming graphene by graphite exfoliation, wherein the methods include: providing a graphite sample having atomic layers of carbon; introducing a salt and a solvent into the space between the atomic layers; expanding the space between the atomic layers using organic molecules and ions from the solvent and the salt; and separating the atomic layers using a driving force to form one or more sheets of graphene; the graphene produced by the methods can be used to form solar cells, to perform DNA analysis, and for other electrical, optical and biological applications.

Abstract: Providing a roaster that operates at temperatures in the range of 800° Celsius to 2000° Celsius with inert, optional oxidizing and reducing gases to treat graphite contaminated with radionuclides including tritium, carbon-14, and chlorine-36. The combination of temperatures and gases allow for the removal of most to substantially all the carbon-14 within the graphite while substantially limiting gasifying the bulk graphite.

Abstract: A process for producing a filmy graphite includes the steps of forming a polyimide film having a birefringence of 0.12 or more and heat-treating the polyimide film at 2,400° C. or higher.

Abstract: A method of fabricating pillared graphene assembles alternate layers of graphene sheets and fullerenes to form a stable protostructure. Energy is added to the protostructure to break the carbon-carbon bonds at the fullerene-to-graphene attachment points of the protostructure and allow the bonds to reorganize and reform into a stable lower energy unitary pillared graphene nanostructure in which open nanotubes are conjoined between graphene sheets. The attachment points may be functionalized using tether molecules to aid in attachment, and add chemical energy to the system. The arrangement and attachment spacing of the fullerenes may be determined using spacer molecules or an electric potential.

Abstract: A method of transferring graphene, the method including: preparing a graphene forming structure including a base member, an oxide layer that is hydrophilic and is formed on the base member, a metal catalyst layer that is hydrophobic and is formed on the oxide layer, and graphene that is formed on the metal catalyst layer; attaching the graphene forming structure on a surface of a first carrier; separating the oxide layer from the metal catalyst layer by applying steam to the graphene forming structure; and removing the metal catalyst layer.

Abstract: Provided is a raw petroleum coke composition as a raw material of an anode carbon material that can improve, when a battery is discharged at a high current, the ratio capable of maintaining the capacity obtained during discharge at a low current. More specifically, provided is a raw petroleum coke composition for an anode carbon material of a lithium ion secondary battery, the raw petroleum coke composition being produced by subjecting a heavy-oil composition to a delayed coking process, and comprising an atomic ratio of hydrogen atoms H to carbon atoms C(H/C atomic ratio) of 0.30 to 0.50, and a micro-strength of 7 to 17% by weight.

Abstract: A method is disclosed for making graphenic carbon particles. The method includes introducing a methane precursor material into a thermal zone, heating the methane precursor material in the thermal zone to form the graphenic carbon particles from the methane precursor material, and collecting the graphenic carbon particles. Apparatus for performing such a method, and graphenic particles produced by the method, are also disclosed.

Abstract: A method is disclosed for making graphenic carbon particles. The method includes introducing a hydrocarbon precursor material capable of forming a two-carbon-fragment species into a thermal zone, heating the hydrocarbon precursor material in the thermal zone to form the graphenic carbon particles from the hydrocarbon precursor material, and collecting the graphenic carbon particles. Apparatus for performing such a method, and graphenic particles produced by the method, are also disclosed.

Abstract: A negative electrode material for a nonaqueous secondary battery capable of realizing a nonaqueous secondary battery having a small charging/discharging irreversible capacity at an initial cycle and exhibiting an excellent high-rate charging/discharging characteristics and an excellent cycle performances is provided. The main component of the material is graphite particles. The median diameter is 5 ?m or more, and 40 ?m or less in the volume-basis particle size distribution based on the laser diffraction/scattering particle size distribution measurement. The tapping density is 0.7 g/cm3 or more. The specific surface area measured by a BET method is 0.2 m2/g or more, and 8 m2/g or less. The average circularity is 0.83 or more, and 1.00 or less. When an electrode is produced by a predetermined method for manufacturing an electrode and, the resulting electrode is subjected to X-ray diffraction, the graphite crystal orientation ratio I110/I004 on the electrode is 0.

Abstract: Solvents for macromolecules generally believed to be insoluble in their pristine form are identified by generation of a “solvent resonance” in the relationship between solvent quality (deduced by Rayleigh scattering) and an intrinsic property of solvents. A local extreme of the solvent resonance identifies the ideal intrinsic property of an ideal solvent which may then be used to select a particular solvent or solvent combination. A solvent for graphene is used in the production of transparent conductive electrodes.

Abstract: A method for preparing a graphene based conductive material and the graphene based conductive material prepared by the method. The method includes: preparing a solid film on a substrate layer by using graphene oxide sol and metal salt solution and/or metal colloidal solution, keeping the solid film separated or without separated from the substrate layer standing for from 30 s to 10000 h in an atmosphere consisting of hydrogen or containing hydrogen with temperature of ?50° C.˜200° C. and hydrogen pressure of 0.01-100 MPa, obtaining the graphene based conductive material. The preparation method can be processed at low temperature and uses cheap hydrogen as reductant, so the preparation process is simple and environment friendly.

Abstract: The present application relates generally to methods for growth of high quality graphene films. In particular, a method is provided for forming a graphene film using a modified chemical vapor deposition process using an oxygen-containing hydrocarbon liquid precursor. Desirably, the graphene films are a single-layer and have a single grain continuity of at least 1 ?m2.

Abstract: An object of the present invention is to solve a problem such as a small crystal size, which is the issue of a conventional method for formation of a film of graphene by a thermal CVD technique using a copper foil as a substrate, and thus providing a carbon film laminate in which graphene having a larger crystal size is formed. The carbon film laminate is configured to include a sapphire (0001) single crystal having a surface composed of terrace surfaces which are flat at the atomic level, and atomic-layer steps, a copper (111) single crystal thin film formed by epitaxial growth on the substrate and graphene deposited on the copper (111) single crystal thin film, and thus enabling formation of graphene having a large crystal size.

Abstract: Disclosed are a process for preparing a solution comprising few-layered graphene, a process for preparing a few-layered graphene solid, and a process for preparing a film thereof.

Abstract: Provided are a graphite material suitable as an electrode material for nonaqueous electrolyte secondary batteries, a carbonaceous material for battery electrodes, and secondary batteries which exhibit excellent charge-discharge cycle characteristics and excellent severe-current-load characteristics. A graphite material which has specific sizes of optically anisotropic and isotropic structures, a specific content ratio between both structures, and various orientation of crystallization; and a carbonaceous material for battery electrodes which is made using the graphite material and which exhibits a large discharge capacity and a small irreversible capacity with the severe-current-load characteristics and cycle characteristics being kept at high levels.

Abstract: A graphite material includes a plurality of graphite particles and a plurality of pores. The plurality of graphite particles and the plurality of pores form a microstructure. A ratio of an elastic modulus to a compression strength of the graphite material ranges from 109 to 138. Preferably, a ratio of a total area of the pores to a whole area of the graphite material in a cross-section of the graphite material ranges from 17.94% to 19.97%.

Abstract: This disclosure includes a process that unexpectedly can produce very inexpensive graphene and a new compound called graphenol in particulate or dispersions in solvents. The process can also produce graphene layers on metallic and nonmetallic substrates. Further, the graphenol and graphene can be utilized to form nanocomposites that yield property improvements exceeding anything reported previously.

Abstract: A process for the production of exfoliated graphite is presented, involving providing a graphite intercalation compound; and exfoliating the graphite intercalation compound by passing the graphite intercalation compound through a plasma which is at a temperature of at least about 6000° C. to bring the graphite intercalation compound to a temperature between about 1600° C. and about 3400° C.

Abstract: A method for growing a graphene nanoribbon on an insulating substrate having a cleavage plane with atomic level flatness is provided, and belongs to the field of low-dimensional materials and new materials. The method includes the following steps. Step 1: Cleave an insulating substrate to obtain a cleavage plane with atomic level flatness, and prepare a single atomic layer step. Step 2: Directly grow a graphene nanoribbon on the insulating substrate having regular single atomic steps. In the method, a characteristic that nucleation energy of graphene on the atomic step is different from that on the flat cleavage plane is used, and conditions, such as the temperature, intensity of pressure and supersaturation degree of activated carbon atoms, are adjusted, so that the graphene grows only along a step edge into a graphene nanoribbon of an adjustable size. The method is mainly applied to the field of new-type graphene optoelectronic devices.

Abstract: [Means for solving] A graphene oxide sheet which changes to a substance having a graphene structure when reduced, and which is obtainable by dispersing a graphene-containing carbon substance using a dispersant to reduce the size of the aggregate units of the graphene-containing carbon substance, and then oxidizing the graphene-containing carbon substance.

Abstract: A method for modifying graphite particles having a prismatic shape or a cylindrical shape characterized by an edge function fe and a basal function fb, said method providing increase of the edge function and lowering of the basal function, wherein the method includes submitting the graphite particles to at least one physical means selected from attrition, jet mill, ball mill, hammer mill, or atomizer mill, in the presence of at least one chemical compound chosen from the group of compounds of the formula MFz, in which M represents an alkaline or alkaline-earth metal and z represents 1 or 2, NaCl and NH4F or a mixture thereof, said compound or compounds being added in solid form, at the beginning of the step using the physical means.

Abstract: A metal-carbon composition including a metal and carbon, wherein the metal and the carbon form a single phase material, characterized in that the carbon does not phase separate from the metal when the single phase material is heated to a melting temperature, the metal being selected from the group consisting of gold, silver, tin, lead, and zinc.

Abstract: A graphite film showing an extremely low average tearing force is more likely to suffer from various kinds of defects, such as splitting, winding deviation, wrinkling, and poor dimensional accuracy, in a step of producing the graphite film and in a step of processing the graphite film. However, these defects can be prevented by using a graphite film that satisfies the following requirements: 1) having an average tearing force of not more than 0.08 N as determined by Trouser tear method in accordance with JIS K7128; and 2) having sag of not less than 5 mm and not greater than 80 mm as determined by a method of film windability evaluation in accordance with JIS C2151.

Abstract: Small particle size expandable graphite materials are described which are highly expandable, as well as methods of making such unique graphite materials. In one embodiment, expandable graphite particles are described having a particle size nominally between about 100 and 200 US mesh, a chromium content of less than 5 parts per million (ppm) and an expansion of about 80 cc/g or greater when heated at about 500° C.

Abstract: The present invention relates to a method for production of graphite bodies. Carbon bodies are formed from a mixture of electric calcined coke particles calcined at a temperature between 1200 and 3000° C. and a binder where the coke particles have sulphur-and nitrogen content varying between 0 and 1.5% by weight and where the coke particles have an average sulphur content less than 0.6% by weight and a nitrogen content of less than 0.6% by weight, baking of the carbon bodies at a temperature between 700 and 1400° C. and graphitizing of the baked carbon bodies at a temperature above 2300° C.

Abstract: The invention relates to a method for producing a graphite-based peptide purification material, which is characterized in that graphite is adjusted to a pH of <7 (acid) by incubation at least once in at least one organic or inorganic acid for at least one minute. The invention further relates to a method for peptide purification, wherein the peptide has a terminal planar aromatic protective group, using graphite in a packed form as the purification material, wherein the method is characterized in that previously acidified graphite (pH<7), which has been produced according to the method for producing a graphite-based peptide purification material, is used as the purification material.

Abstract: Disclosed is a method of manufacturing graphene, a transparent electrode and an active layer including the graphene, and a display, an electronic device, an optoelectronic device, a solar cell, and a dye-sensitized solar cell including the transparent electrode and the active layer. The method of manufacturing graphene includes: (a) preparing a subject substrate; (b) forming a metal thin film on the subject substrate and heat-treating the metal thin film to increase the grain size of the metal thin film; (c) supplying a carbon source material on the metal thin film; (d) heating the supplied carbon source material, the subject substrate, and the metal thin film; (e) diffusing carbon atoms generated from the heated carbon source material due to thermal decomposition into the metal thin film; and (f) forming graphene on the subject substrate by the carbon atoms diffused through the metal thin film.

Abstract: Graphene which is permeable to lithium ions and can be used for electric appliances is provided. A carbocyclic ring including nine or more ring members is provided in graphene. The maximum potential energy of the carbocyclic ring including nine or more ring members to a lithium ion is substantially 0 eV. Therefore, the carbocyclic ring including nine or more ring members can function as a hole through which lithium ions pass. When a surface of an electrode or an active material is coated with such graphene, reaction of the electrode or the active material with an electrolyte can be suppressed without interference with the movement of lithium ions.

Abstract: A process for producing a filmy graphite includes the steps of forming a polyimide film having a birefringence of 0.12 or more and heat-treating the polyimide film at 2,400° C. or higher.

Abstract: Technologies are generally described for forming graphene and structures including graphene. In an example, a system effective to form graphene may include a chamber adapted to receive graphite oxide. The system may also include a source of an inert gas and a source of hydrogen, which may both be configured in communication with the chamber. A processor may be configured in communication with the chamber, the inert gas source and/or the hydrogen source. The processor may be further configured to control the flow of the inert gas from the first source through the chamber under first sufficient reaction conditions to remove at least some oxygen from the atmosphere of the chamber. The processor may also be configured to control the flow of the hydrogen from the second source to the graphite oxide in the chamber under second sufficient reaction conditions to form graphene from the graphite oxide.

Abstract: The present invention relates a method for producing a graphite intercalation compound (GIC) and to the production of graphene using the same. The method of the present invention comprises the following steps: (a) obtaining alkaline metals or alkaline metal ions, or alkaline earth metals or alkaline metal ions, from alkaline metal salts or alkaline earth metal salts; (b) forming a graphite intercalation compound using the alkaline metals or alkaline metal ions, or the alkaline earth metals or alkaline earth metal ions; and (c) dispersing the graphite intercalation compound so as to obtain graphene. As the method of the present invention uses salts which are inexpensive and safe, graphite intercalation compounds can be easily produced at a low cost, and the graphene can be obtained from the thus-produced compounds, thereby reducing the costs of producing the graphene and enabling the easy mass production of the graphene.

Abstract: There is provided a method for producing a graphite material and a graphite material produced by the method The method includes a kneading step of adding a hydrophobic binding material to a first carbonaceous raw material containing coke powder, followed by heat kneading to obtain a mixture, a pulverizing step of pulverizing the mixture obtained in the kneading step to obtain a second carbonaceous raw material, a granulating step of obtaining a granulated powder using the second carbonaceous raw material obtained in the pulverizing step, a hydrophilic binding material and a solvent, a molding step of subjecting the granulated powder obtained in the granulating step to cold isostatic press molding to obtain a molded body, a burning step of burning the molded body obtained in the molding step to obtain a burnt product, and a graphitizing step of graphitizing the burnt product obtained in the burning step.

Abstract: There are provided a cluster of thin sheet graphite crystals or the like which is useful as an electrode material for lithium ion batteries, hybrid capacitors and the like, and a method for efficiently producing the same at high productivity. The method is one for producing a cluster of thin sheet graphite crystals composed of aggregates in such a state that thin sheet graphite crystals extend from the inside toward the outside, comprising charging a powdery and/or particulate material of an organic compound pre-baked to an extent of containing remaining hydrogen in a graphite vessel, and subjecting the powdery and/or particulate material together with the vessel to hot isostatic pressing treatment (HIP treatment) using a compressed gas atmosphere under the predetermined conditions.

Abstract: The present invention relates to a graphite particle and a carbon-graphite composite particle both suitable for use in electrode for lithium ion secondary battery, as well as to processes for producing these particles. The graphite particle of the present invention has an average particle diameter of 5 to 50 ?m, wherein one or more recesses having a depth of 0.1 to 10 ?m are formed in the surface. The graphite particle is produced by a mixing step for mixing raw material graphite particles and recess-forming particles, a press molding step for press-molding the mixture composed of the raw material graphite particles and the recess-forming particles to obtain a molded article, a pulverization step for pulverizing the molded article, and a separation step for separating and removing the recess-forming particles from the pulverized molded article.

Abstract: A method of forming a graphitic carbon body employs compression and resistance heating of a stock blend of a carbon material and a binder material. During molding of the body, resistance heating is accompanied by application of mechanical pressure to increase the density and carbonization of the resulting preform body. The preform can then be subjected to a graphitization temperature to form a graphite article.

Abstract: An electrode active material for an all solid state secondary battery, which is able to have the controlled orientation of a crystal face at the interface between an electrode layer and an electrolyte layer in order to enhance the battery performance, and an all solid state secondary battery including the electrode active material. The electrode active material includes a carbon material having an intensity ratio (P002/P100) of 600 or less between the X-ray diffraction peak intensity P002 in the (002) plane and the X-ray diffraction peak intensity P100 in the (100) plane, which are obtained when a surface of a compact prepared by compression molding of a powder of the carbon material at a pressure of 110 MPa is irradiated with X-ray. The all solid state secondary battery includes a positive electrode, a negative electrode, and a solid electrolyte, and the negative electrode contains the electrode active material.

Abstract: Disclosed are a method for preparing pure graphene using chemical bonding between graphite oxide and metal oxide nanoparticles, and graphene and nanoparticles having a quasi metal oxide-graphene core-shell prepared therefrom. The disclosed method for preparing graphene allows chemical bonding and separation through a simple acid treatment process using inexpensive materials. Also, because the reaction can be carried out at low temperature, the processing cost is low. And, pure graphene with few impurities can be prepared quickly in large scale.

Abstract: Carbon nanostructures are synthesized from carbon-excess explosives having a negative oxygen balance. A supercritical fluid provides an environment that safely dissolves and decomposes the explosive molecules into its reactant products including activated C or CO and provides the temperature and pressure for the required collision rate of activated C atoms and CO molecules to form carbon nanostructures such as graphene, fullerenes and nanotubes. The nanostructures may be synthesized without a metal reactant at relatively low temperatures in the supercritical fluid to provide a cost-effective path to bulk fabrication. These nanostructures may be synthesized “metal free”. As the supercritical fluid provides an inert buffer that does not react with the explosive, the fluid is preserved. Once the nanostructures are removed, the other reaction products may be removed and the fluid recycled.

Abstract: A crystalline carbon material with controlled interlayer spacing and a method of manufacturing the crystalline carbon material are disclosed. The crystalline carbon material has peaks of a (002) plane at 2?=23°±5.0° and 2?=26.5°±1.0° when X-ray diffraction is measured using a CuK? ray. The peak height at 2?=23°±5.0° is higher than the one at 2?=26.5°±1.0°.

Abstract: The present invention relates to novel nanocomposite materials, methods of making nanocomposites and uses of nanocomposite materials.

Abstract: Methods for producing carbon films are disclosed herein. The methods include treating a carbon nanostructure with one or more dispersing agents, filtering the solution through a filter membrane to form the carbon film, releasing the carbon film from the filter membrane, and transferring the film onto a desired substrate without the use of sonication. Carbon films formed by said methods are also disclosed herein.