Abstract: Provided are a method for producing artificial graphite through a vertical graphitization furnace with easy circulation of inert gas, uniform heating and no damage to the furnace; and particulates used therefor. The method comprises steps of: introducing graphitizable particulates having average particle diameter of 3 to 30 mm into an inside of the furnace from upper part thereof, heating the particulates at 2200° C. to 3200° C. while making inert gas flow from lower part toward upper part thereof to graphitize the particulates, and removing the graphite through lower part thereof. The particulates have average particle diameter of 3 to 30 mm and are obtained by granulating mixture comprising 100 wt parts of graphitizable carbonaceous substance powder having average particle diameter of 10 to 20 ?m, 3 to 20 wt parts of binder decomposable at lower than 1000° C., and 5 to 30 wt parts of liquid which can dissolve the binder.

Abstract: A process for producing GNP-based polymeric nanocomposites for electromagnetic applications such as shielding and/or absorption of the energy associated to electromagnetic fields envisages a plurality of steps that include: controlled synthesis, for optimizing the morphological and electrical properties thereof, of graphene nanoplatelets (GNPs) to be used as nanofillers in a polymeric matrix; selection of the polymeric matrix so as to optimize its chemical compatibility with the type of GNPs thus obtained; production via the solution-processing technique of GNP-based polymeric nanocomposites with dielectric permittivity and electric conductivity controlled and predictable via the equivalent-effective-medium model by calibrating the parameters of the model for the specific type of polymeric matrix and GNPs used.

Abstract: A process for producing fine particles with a high aspect ratio and/or a low specific surface area includes use of a jet mill. An alkaline grinding aid is added to a grinding gas before the grinding gas is fed into a grinding chamber of the jet mill. The process includes micronization of particles of layered structure material having an interplanar distance ranging from 0.30 nm to 0.40 nm as measured by X-ray diffraction method.

Abstract: Technologies described herein are generally related to graphene production. In some examples, a system is described that may include a first container, a second container, and/or a chamber. The first container may include a first solution with a reducing agent, while the second container may include a second solution with graphene oxide. The chamber may be in operative relationship with the first and the second containers, and configured effective to receive the first and second solutions and provide reaction conditions that facilitate contact of the first and second solutions at an interfacial region sufficient to produce graphene at the interfacial region.

Abstract: The green synthesis of reduced graphene oxide nanoparticles using Nigella sativa seed extract comprises the steps of mixing a quantity of soot or other carbon source in an acid solution while stirring to obtain a solution; adding a first oxidant gradually into the solution to oxidize the soot and obtain a suspension; stirring the suspension while maintaining the temperature of the suspension at about 35° C.; adding Nigella sativa seed extract to the suspension while raising the temperature of the suspension to about 60° C.; adding hydrogen peroxide to the suspension; and isolating the reduced graphene oxide nanoparticles by centrifugation.

Abstract: A conductive circuit containing a polymer composite, which contains at least one polymer and a modified graphite oxide material, containing thermally exfoliated graphite oxide having a surface area of from about 300 m2/g to 2600 m2/g, and a method of making the same.

Abstract: A method of preparing a graphene material. The method includes: (1) preparing a liquid polyacrylonitrile (LPAN) solution, stirring the LPAN solution to yield a cyclized polyacrylonitrile solution; (2) stirring the cyclized LPAN solution at between 200 and 300° C. to yield a thermally-oxidized polyacrylonitrile; (3) grinding and sieving the thermally-oxidized polyacrylonitrile, and drying a resulting product at room temperature, to yield a thermally-oxidized precursor; (4) calcining the thermally-oxidized precursor in the presence of an inert gas flow of between 10 and 500 mL/min for between 1 and 24 hrs at the temperature of between 400 and 1000° C., to yield a carbonized precursor; and (5) calcining the carbonized precursor in the presence of an inert gas flow of between 10 and 500 mL/min for between 1 and 10 hrs at the temperature of between 1000 and 3000° C., to yield a graphene material.

Abstract: Provided is a method of producing an integral 3D graphene-carbon hybrid foam, comprising: (a) mixing multiple particles of a graphitic material and multiple particles of a solid polymer carrier material to form a mixture in an impacting chamber of an energy impacting apparatus; (b) operating the energy impacting apparatus to peel off graphene sheets from the graphitic material and transferring the graphene sheets to surfaces of solid polymer carrier material particles to produce graphene-coated polymer particles; (c) recovering the graphene-coated polymer particles from the impacting chamber and consolidating the graphene-coated polymer particles into a desired shape of graphene-polymer composite structure; and (d) pyrolyzing the shape of graphene-polymer composite structure to thermally convert the polymer into carbon or graphite that bonds the graphene sheets to form the integral 3D graphene-carbon hybrid foam.

Abstract: The invention provides methods for the combustion synthesis (CS) of graphene by a novel exothermic self-sustained reaction between a refractory ceramic compound and a carbon-containing polymer under an inert gas atmosphere. The synthesis of graphene was confirmed by both transmission electron microscopy and Raman spectroscopy. The graphene produced has very low (<1 wt. %) oxygen content. Fluorocarbon gases released due to decomposition of the carbon-containing polymer in the combustion wave can reduce the ceramic to a gas and mesoporous carbon particles and graphene layers. The method does not require an external energy source because it occurs in a self-sustained synergetic manner after ignition. The methods are flexible in terms of tuning the synthesis conditions for desired products, and the method can be scaled to provide kilogram quantities.

Abstract: Provided is a method for room-pressure and low-temperature preparation of graphene, comprising: heat treating a compound of graphite oxide and sulfuric acid in either room pressure or negative pressure at a temperature between 50 and 400° C., thus converting graphite oxide into graphene. Also provided is a method for low-temperature preparation of a graphene composite material. The acquired graphene and graphene composite material are applicable in optical materials, electrically-conductive materials, sensor materials, catalytic materials, battery materials, and supercapacitor materials.

Abstract: A preparation method of a graphene nanoribbon on h-BN, comprising: 1) forming a h-BN groove template with a nano ribbon-shaped groove structure on the h-BN by adopting a metal catalysis etching method; 2) growing a graphene nanoribbon in the h-BN groove template by adopting a chemical vapor deposition method. In the present invention, a CVD method is adopted to directly prepare a morphology controllable graphene nanoribbon on the h-BN, which helps to solve the long-term critical problem that the graphene is difficult to nucleate and grow on an insulating substrate, and to avoid the series of problems introduced by the complicated processes of the transferring of the graphene and the subsequent clipping manufacturing for a nanoribbon and the like.

Abstract: A method for preparing photoluminescent carbon nanodots includes preparing and drying a sample, ashing the sample, extracting the ashed sample with solvent, filtering the extracted sample, concentrating the filtered sample, dissolving the sample in water, and freeze-drying the dissolved sample. The sample is preferably a food waste residue or animal excrement.

Abstract: A method of forming graphene comprises patterning an organic material monolayer disposed on a first substrate to yield a patterned organic material monolayer, and supplying thermal energy to the patterned organic material monolayer. The thermal energy is sufficient to carbonize the monolayer to form a patterned layer of graphene on said substrate.

Abstract: A method of producing single or few-layer graphene comprises exfoliating graphite with a polymer to form a graphene-polymer composite and subsequently treating the composite to disassociate graphene. The exfoliation process is conducted using sonication. The graphene is disassociated from the polymer by a treatment step such as acid hydrolysis. The method results in highly pure graphene.

Abstract: The present invention relates to a process for preparing a graphene nanoribbon, which comprises: (a) providing at least one aromatic monomer compound which is selected from at least one polycyclic aromatic monomer compound, at least one oligo phenylene aromatic monomer compound, or combinations thereof, on a solid substrate, (b) polymerization of the aromatic monomer compound so as to form at least one polymer on the surface of the solid substrate, (c) at least partially cyclodehydrogenating the one or more polymers of step (b), wherein at least step (b) is carried out at a total pressure p(total) of at least 1×10?9 mbar; and a partial oxygen pressure p(O2) and partial water pressure p(H2O) which satisfy the following relation: p(O2)×p(H20)<3×10?14 mbar2.

Abstract: The present invention relates to a method for preparing reduced graphene oxide from graphene oxide using a solid hydrazine derivative.

Abstract: An object of the present invention is to provide an anisotropic heat conductive composition comprising: resin; and graphite fillers dispersed into the resin, wherein the graphite fillers each have a maximum diameter A in parallel with a basal plane of each of the graphite fillers and a maximum length C perpendicular to the basal plane, an average of the maximum diameters A ranges from 1 ?m to 300 ?m, an average ratio of the maximum diameter A to the maximum length C represented by A/C is at least 30, a content of the graphite fillers is 20 mass % to 40 mass %, and an average of a smaller angle made by the basal plane and a sheet surface of the sheet anisotropic heat conductive composition is less than 15°.

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: An intercalated graphite compound composition, comprising a layered graphite with interlayer spaces or interstices and an intercalant residing in at least one of said interstices, wherein said intercalant comprises a carboxylic acid and an oxidant selected from Li2FeO4, Na2FeO4, K2FeO4, LixCoO4, NaxCoO4, KxCoO4, LixNiO4, NaxNiO4, KxNiO4, or a combination thereof. This compound can be produced in an environmentally benign process. The compound can be further treated to produce separate graphene sheets.

Abstract: The present invention relates to a method for preparing graphite layers, comprising the step of heating at least one monolayer with low-molecular weight aromatics and/or low-molecular weight heteroaromatics crosslinked in the lateral direction under vacuum or inert gas to a temperature of >800 K, and to graphite layers which are obtainable by this method.

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: A method of surface modifying graphene is disclosed and includes placing powder-like graphene into a closed container, heating up to a preset impurity detaching temperature higher than 100° C. so as to detach the impurity from the surface of graphene, further adjusting the treatment temperature to a preset surface modifying temperature, and injecting the gaseous surface modifying agent to be physically adsorbed by the surface of graphene. Thus, surface modified graphene is formed. The surface modifying temperature is higher than the sublimation temperature of the surface modifying agent and less than the decomposition temperature of the surface modifying agent. Therefore, the present invention is simpler and safer because of only physical adsorption used and no chemical reaction involved. Dispersibility of surface modified graphene in the solution is greatly increased to improve uniformity and enhance the performance of the final product formed of surface modified graphene.

Abstract: A composite lubricating material including at least a graphite-based carbon material and/or graphene-like graphite exfoliated from the graphite-based carbon material dispersed in a base material. The graphite-based carbon material is characterized by having a rhombohedral graphite layer (3R) and a hexagonal graphite layer (2H), wherein a Rate (3R) of the rhombohedral graphite layer (3R) and the hexagonal graphite layer (2H), based on an X-ray diffraction method, which is defined by following Equation 1 is 31% or more: Rate (3R)=P3/(P3+P4)×100 ??Equation 1 wherein P3 is a peak intensity of a (101) plane of the rhombohedral graphite layer (3R) based on the X-ray diffraction method, and P4 is a peak intensity of a (101) plane of the hexagonal graphite layer (2H) based on the X-ray diffraction method.

Abstract: The present invention provides a process for producing a two-dimensional nanomaterial by chemical vapor deposition (CVD), the process comprising contacting a substrate in a reaction chamber with a first flow which contains hydrogen and a second flow which contains a precursor for said material, wherein the contacting takes place under conditions such that the precursor reacts in the chamber to form said material on a surface of the substrate, wherein the ratio of the flow rate of the first flow to the flow rate of the second flow is at least 5:1. Two-dimensional nanomaterials obtainable by said process are also provided, as well as devices comprising said nanomaterials.

Abstract: A thermal and electrical conducting apparatus includes a few-layer graphene film having a thickness D where D?1.5 nm and a plurality of carbon nanotubes crystallographically aligned with the few-layer graphene film.

Abstract: A thermal and electrical conducting apparatus includes a few-layer graphene film having a thickness D where D?1.5 nm and a plurality of carbon nanotubes crystallographically aligned with the few-layer graphene film.

Abstract: A method of making an anode includes the steps of providing fibers from a carbonaceous precursor, the carbon fibers having a glass transition temperature Tg. In one aspect the carbonaceous precursor is lignin. The carbonaceous fibers are placed into a layered fiber mat. The fiber mat is fused by heating the fiber mat in the presence of oxygen to above the Tg but no more than 20% above the Tg to fuse fibers together at fiber to fiber contact points and without melting the bulk fiber mat to create a fused fiber mat through oxidative stabilization. The fused fiber mat is carbonized by heating the fused fiber mat to at least 650° C. under an inert atmosphere to create a carbonized fused fiber mat. A battery anode formed from carbonaceous precursor fibers is also disclosed.

Abstract: Rigid foam insulating products and processes for making such insulation products are disclosed. The foam products are formed from a polymer, a blowing agent, and nano-graphite. The nano-graphite has a size in at least one dimension less than about 100 nm and, in exemplary embodiments may be an intercalated, expanded nano-graphite. In addition, the nano-graphite may include a plurality of nanosheets having a thickness between about 10 to about 100 nanometers. The nano-graphite acts as a process additive to improve the physical properties of the foam product, such as thermal insulation and compressive strength. In addition, the nano-graphite in the foam controls cell morphology and acts as a nucleating agent in the foaming process. Further, the nano-graphite exhibits overall compound effects on foam properties including improved insulating value (increased R-value) for a given thickness and density and improved ultraviolet (UV) stability.

Abstract: Polymeric article reinforced with a reinforcing component. The reinforcing component includes a composition made from at least one polymer and graphene sheets.

Abstract: A graphene sheet is provided. The graphene sheet includes a carbon lattice and a spatial distribution of defects in the carbon lattice. The spatial distribution of defects is configured to tailor the buckling properties of the graphene sheet.

Abstract: The present invention resolves the problem by using a multilayer-structured carbon material, as a nonaqueous electrolytic solution secondary battery negative electrode, which satisfies the following (a) and (b): (a) (Void fraction calculated from DBP oil absorption)/(Void fraction calculated from tapping density) is less than 1.01; and (b) Surface oxygen content (O/C) determined by X-ray photoelectron spectroscopy is 1.5 atomic % or more.

Abstract: A composite wafer including a carrier substrate having a graphite core and a monocrystalline semiconductor substrate or layer attached to the carrier substrate and a corresponding method for manufacturing such a composite wafer is provided.

Abstract: The invention includes a controlled graphene film growth process including the production on the surface of a substrate of a layer of a metal having with carbon a phase diagram such that, above a molar concentration threshold ratio CM/CM+CC, where CM is the molar metal concentration in a metal/carbon mixture and CC is the molar carbon concentration in the mixture, a homogeneous solid solution is obtained. The metal layer is exposed to a controlled flux of carbon atoms or carbon-containing radicals or carbon-containing ions at a temperature such that the molar concentration ratio obtained is greater than the threshold ratio to obtain a solid solution of carbon in the metal. The process further includes an operation for modifying the phase of the mixture into two phases, a metal phase and a graphite phase, leading to the formation of at least a lower graphene film at the metal layer incorporating carbon atoms-substrate interface and an upper graphene film at the surface of the metal layer.

Abstract: The present invention relates to a nitrate salt-based process for preparing a graphite oxide. The invention nitrate salt-based process employs starting materials comprising a sulfuric acid, an inorganic nitrate salt, an amount of water, a first amount of chlorate salt, and a graphite.

Abstract: Graphene transferring methods, a device manufacturing method using the same, and substrate structures including graphene, include forming a catalyst layer on a first substrate, forming a graphene layer on the catalyst layer, forming a protection metal layer on the graphene layer, attaching a supporter to the protection metal layer, separating the first substrate from the catalyst layer such that the protection metal layer, the graphene layer, and the catalyst layer remain on the supporter, removing the catalyst layer from the supporter, and transferring the protection metal layer and the graphene layer from the supporter to a second substrate.

Abstract: A method for controllable layer-by-layer removal of graphene layers is provided. The method includes the steps of: disposing a single-layer or multi-layer graphene on a heat source, arranging graphene layer or layers in a sealed chamber filled with ozone gas, and removing a targeted area of graphene with a laser. The method provides low-temperature removal of graphene layer-by-layer. The heat source, laser, and the highly oxidizing ozone gas selectively control the removal of graphene layers.

Abstract: The present invention provides a method for preparing graphene, including reacting graphite in an acid solution in which an oxidant is present so as to obtain a graphene. Compared with the prior art, the advantages of the present invention reside in that, the graphene prepared by the method of the present invention has excellent quality and substantially increased yield and production rate, as compared with mechanical stripping, epitaxial growth, and chemical vapor deposition; and the graphene prepared by the method of the present invention has significantly improved quality, substantially reduced structural defects, and significantly increased conductivity, as compared with oxidation-reduction preparation in the solution-phase; besides, the method is also advantageous for a simple process, mild conditions, low cost, and very easy for scale production.

Abstract: A functionalised graphene oxide and a method of making a functionalized graphene oxide comprising: (i) oxidizing graphite to form graphite oxide wherein the graphene sheets which make up the graphite independently of each other have a basal plane fraction of carbon atoms in the sp2-hybridised state between 0.1 and 0.9, wherein the remainder fraction comprises sp3-hybridised carbon atoms which are bonded to oxygen groups selected from hydroxyl and/or epoxy and/or carboxylic acid; and (ii) exfoliating and in-situ functionalizing the graphite oxide surface with one or more functional groups such that fictionalization of the surface is effected at a concentration greater than one functional group per 100 carbon atoms and less than one functional group per six carbon atoms. The functionalized graphene oxide is dispersible at high concentrations in appropriate solvents without aggregating or precipitating over extended periods at room temperature.

Abstract: A graphitization furnace (100) includes: split electrodes (122) that are conductive and are provided so as to be freely movable; crucibles (120) that are conductive and that contain carbon powder, with a bottom end portion (122a) of each split electrode (122) being buried in the carbon powder; upper electrodes (190) that are positioned so as to face a split electrode (122); lower electrodes (192) that are positioned so as to face a crucible (120); and a power supply unit (132) that, when a bottom end portion (190a) of an upper electrode (190) is placed in contact with a top end portion (122b) of a split electrode (122) and a top end portion (192a) of a lower electrode (192) is placed in contact with a base portion (120b) of a crucible (120), applies a voltage between the upper electrode (190) and the lower electrode (192).

Abstract: The present invention provides a process for the preparation of graphene or graphene-like fragments of another layered structure, said process comprising the step of mixing and grinding graphite or said other layered structure with at least one ionic liquid. The invention also provides the use of grinding in ionic liquids in such a process and products formed or formable by such methods.

Abstract: Disclosed is an anode for secondary batteries comprising a combination of an anode active material having a relatively low charge/discharge voltage and a relatively low hardness (A) and an anode active material having a relatively high charge/discharge voltage and a relatively high hardness (B), wherein the anode active material (A) is surface-coated with carbon having a high hardness or a composite thereof, and a particle size of the anode active material (B) is smaller than a size of a space formed by the anode active materials (A) arranged in a four-coordination. The anode provides an electrode that prevents lithium precipitation caused by overvoltage, improves ionic conductivity as well as electric conductivity and exhibits superior capacity.

Abstract: A method of manufacturing a graphene oxide composite fiber includes forming a supporting fiber having positive charges thereon; forming a solution containing graphene oxide having a negative charge thereon to provide a graphene oxide-containing solution; coating the supporting fiber with the graphene oxide-containing solution; and permitting self-assembly of the graphene oxide of the graphene oxide -containing solution and the supporting fiber by an attraction between the positive and negative charges to form the graphene oxide composite fiber. The method may include coating the supporting fiber with a solution containing a material having an amine group to provide a positive surface charge on the supporting fiber. The method may include reducing the graphene oxide composite fiber to a graphene composite fiber, such as by one of a thermal reduction method, an optical reduction method, and a chemical reduction method.

Abstract: A simple and easy method for fabricating graphene quantum dots with uniformed size and high quality of emission property comprises steps of, mixing graphite powders with metallic hydrate salts, forming an intercalation compound of graphite wherein metal ions are inserted by heating the mixed solution, and removing the metal ions from the intercalation compound of graphite. The graphene quantum dots is applicable to the development of electronic products in next generation such as display devices, recording devices, various sensors and nanocomputers and is applicable to biological and medicinal field as well.

Abstract: A graphite carbon composite material including a graphite material having diversity in the sizes of optical anisotropic structure and optical isotropic structure, the ratio thereof, and crystal direction, and a carbon material on the way to a graphitized structure of easily-graphitizable carbon. Also disclosed is a carbon material for a battery electrode, a past for an electrode, an electrode, a battery, a lithium ion secondary battery and a method of producing the graphite carbon composite material.

Abstract: A graphite composite material obtained by mixing graphite material 1 having diversity in the sizes of optical anisotropic structure and optical isotropic structure, the ratio thereof, and crystal direction, and graphite material 2 having a rhombohedron structure, which is different from graphite material 1 and has an average interplanar spacing d002 of plane (002) of 0.3354 nm to 0.3370 nm measured by the powder X-ray diffraction method and Lc of 100 nm or more. Also disclosed is a carbon material for a battery electrode, a paste for an electrode, an electrode, a battery, a lithium ion secondary battery and a method of producing the graphite composite material.

Abstract: The present invention relates to a nano-graphite plate structure with N graphene layers stacked together, where N is 30 to 300. The nanometer nano-graphite structure has a tap density of 0.1 g/cm3 to 0.01 cm3, a thickness of 10 nm to 100 nm, and a lateral dimension of 1 ?m to 100 ?m. The ratio of the lateral dimension to the thickness is between 10 and 10,000. The oxygen content is less than 3 wt %, and the carbon content is larger than 95 wt %. The nano-graphite plate structure has both the excellent features of the graphene and the original advantages of easy processability of the natural graphite so as to be broadly used in various application fields.

Abstract: A reliable graphene film that provides complete semiconductive properties without mixing of metallic properties, redacts an off current, achieves a high current on/off ratio of 105 or more sufficient for practical use, and prevents variations in electric properties is obtained. In a grapheme film 3, a plurality of ribbon-shaped graphenes 3a having a longitudinal edge structure of as arm chair type constitute a network structure, and the grapheme 3a includes three or more six-membered rings of carbon atoms bonded in parallel in a short direction and has a width of 0.7 nm or more.

Abstract: A graphite material for a negative electrode of a lithium-ion secondary battery is provided. A ratio Lc(112)/Lc(006) defined as a ratio of expansion of graphene sheets to sheet displacement ranges from 0.08 to 0.11, both inclusive. A crystallite size Lc(006) calculated from a wide-angle X-ray diffraction line ranges from 30 nm to 40 nm, both inclusive. An average particle size ranges from 3 ?m to 20 ?m, both inclusive.

Abstract: Biogenic activated carbon compositions disclosed herein comprise at least 55 wt % carbon, some of which may be present as graphene, and have high surface areas, such as Iodine Numbers of greater than 2000. Some embodiments provide biogenic activated carbon that is responsive to a magnetic field. A continuous process for producing biogenic activated carbon comprises countercurrently contacting, by mechanical means, a feedstock with a vapor stream comprising an activation agent including water and/or carbon dioxide; removing vapor from the reaction zone; recycling at least some of the separated vapor stream, or a thermally treated form thereof, to an inlet of the reaction zone(s) and/or to the feedstock; and recovering solids from the reaction zone(s) as biogenic activated carbon. Methods of using the biogenic activated carbon are disclosed.

Abstract: A method of preparing functionalized graphene, comprises treating graphene with an alkali metal in the presence of an electron transfer agent and coordinating solvent, and adding a functionalizing compound. The method further includes quenching unreacted alkali metal by addition of a protic medium, and isolating the functionalized graphene.