1402 results about "Graphite particle" patented technology

A process for producing nano-scaled graphene plates with each plate comprising a sheet of graphite plane or multiple sheets of graphite plane with the graphite plane comprising a two-dimensional hexagonal structure of carbon atoms. The process includes the primary steps of: (a) providing a powder of fine graphite particles comprising graphite crystallites with each crystallite comprising one sheet or normally a multiplicity of sheets of graphite plane bonded together; (b) exfoliating the graphite crystallites to form exfoliated graphite particles, which are characterized by having at least two graphite planes being either partially or fully separated from each other; and (c) subjecting the exfoliated graphite particles to a mechanical attrition treatment to further reduce at least one dimension of the particles to a nanometer scale, <100 nm, for producing the nano-scaled graphene plates.

A flame retardant, intumescent pressure sensitive adhesive (PSA) composition for EMI shielding gaskets, tapes, wraps, and the like. The composition is formulated as an admixture of: (a) a PSA component; (b) a halogenated first flame retardant component; (c) a metal-based second flame retardant component; and (d) a filler component of expandable, intercalated graphite particles. In a representative embodiment the PSA component (a) is acrylic-based, the halogenated first flame retardant component (b) is a polybrominated diphenyl compound such as decabromodiphenyl oxide or decabromodiphenyl ether, the metal oxide-based second flame retardant component (c) is antimony oxide, antimony trioxide, or antimony pentoxide, and the filler component (d) is graphite flake.

The invention relates to expanded graphite and methods of making the graphite and products that can be made from the graphite made from the inventive process. The invention includes the step of introducing a fluid into at least one of a plurality of interstices of graphite flake, wherein the fluid comprises at least one of a sub-critical point fluid, a near critical point fluid, or a supercritical fluid. The graphite flake is also intercalated with an intercalant and optionally an oxidizing agent. The invention may further include novel techniques of exfoliating the graphite. The invention may be practiced to make nano-sized graphite particles and also graphite composites. Preferred composites which may be made in accordance with the invention include conductive polymeric composites (thermally or electrically), paint composites, battery composites, capacitor composites, and pollution abatement catalyst support composites.

The invention relates to a lithium ion battery silicon-based composite anode material, a preparation method of the lithium ion battery silicon-based composite anode material, and a battery. The lithium ion battery silicon-based composite anode material adopts an embedded composite core-shell structure, a core has a structure formed by embedding nano silicon particles into a gap of an inner layer of hollowed graphite, and a shell is made from a non-graphite carbon material. According to the silicon-based composite anode material, mechanical grinding, mechanical fusing, isotropic compression processing and carbon coating technologies are combined, so that the nano silicon particles can be successfully embedded into the inner layer of the graphite and the surfaces of graphite particles are uniformly coated; the high-performance silicon-based composite anode material is obtained and is excellent in cycle performance (the 300-times cycle capacity retention ratio is more than 90%) and high in first efficiency (more than 90%); in addition, the silicon-based composite anode material is high in specific energy and compaction density, and can meet the requirements of a high-power density lithium ion battery; the preparation process is simple, the raw material cost is low, and the environment is protected.

Disclosed is a negative active material for a rechargeable lithium battery that includes graphite particles, silicon micro-particles attached on the graphite particles and a carbon film partially or totally coated on the graphite particles.

This invention provides a graphite or graphite-carbon particulate for use as a lithium secondary battery anode material having a high-rate capability. The particulate is formed of a core carbon or graphite particle and a plurality of satellite carbon or graphite particles that are each separately bonded to the core particle wherein the core particle is spherical in shape, slightly elongate in shape with a major axis-to-minor axis ratio less than 2, or fibril in shape, and wherein the satellite particles are disc-, platelet-, or flake-like particles each containing a graphite crystallite with a crystallographic c-axis dimension Lc and a lateral dimension. Preferably, Lc is less than 100 nm and the flake/platelet lateral dimension is less than 1 μm. The core particle may be selected from natural graphite, artificial graphite, spherical graphite, graphitic coke, meso-carbon micro-bead, soft carbon, hard carbon, graphitic fibril, carbon nano-fiber, carbon fiber, or graphite fiber. Preferably, the flat-shaped particles are randomly oriented with respect to one another.

An object is to increase the conductivity of an electrode including active material particles and the like, which is used for a battery. Two-dimensional carbon including 1 to 10 graphenes is used as a conduction auxiliary agent, instead of a conventionally used conduction auxiliary agent extending only one-dimensionally at most, such as graphite particles, acetylene black, or carbon fibers. A conduction auxiliary agent extending two-dimensionally has higher probability of being in contact with active material particles or other conduction auxiliary agents, so that the conductivity can be improved.

Disclosed is a negative active material for a rechargeable lithium battery including a composite of a graphite particle and at least one supermicroparticle, wherein the supermicroparticle has a diameter in the range of 1 nm to 100 nm, is produced using an evaporation method under a gas atmosphere, and includes elements alloyable with lithium.

The present invention relates to a negative active material for a rechargeable lithium battery, a method of manufacturing the negative active material, and a rechargeable lithium battery including the negative active material. The negative active material includes a sphere-shaped first graphite particle that a first particle precursor, a flake-shaped graphite piece, is linked to each other; and at least one second particle dispersed between the flake-shaped graphite pieces inside the sphere-shaped first graphite particle and selected from the group consisting of at least one element particle selected from the group consisting of Si, Sn, Al, Ge, Pb, and combinations thereof; at least one element compound particle selected from the group consisting of Si, Sn, Al, Ge, Pb, and combinations thereof; a composite particle including at least one element selected from the group consisting of Si, Sn, Al, Ge, Pb, and combinations thereof; a carbon composite particle including at least one element selected from the group consisting of Si, Sn, Al, Ge, Pb, and combinations thereof; and a combination particle thereof.

The present invention provides a carbon-cladded composite composition for use as a fuel cell flow field plate or bipolar plate. In one preferred embodiment, the composition comprises a core composite layer sandwiched between two clad layers, wherein (a) the clad layer comprises a conductive carbon or graphite material (e.g., carbon nano-tubes, nano-scaled graphene plates, graphitic nano-fibers, and fine graphite particles); (b) the core composite layer comprises a matrix resin and a conductive filler present in a sufficient quantity to render the composite layer electrically conductive with an electrical conductivity no less than 1 S/cm (preferably no less than 100 S/cm); and (c) the composition has a planar outer surface on each clad side having formed therein a fluid flow channel.

The object of the present invention is to provide a nonaqueous electrolyte secondary battery which has excellent balance of general performance with respect to performance including durability, capacity, resistance, and output characteristics. Provided is a nonaqueous electrolyte battery comprising a positive electrode and a negative electrode each being capable of occluding and releasing metal ions, and a nonaqueous electrolyte solution, wherein the nonaqueous electrolyte solution contains an electrolyte, a nonaqueous solvent, and at least one compound selected from the group consisting of a compound having a fluorosulfonyl structure (—SO₂F), a difluorophosphate, and an isocyanate compound, and wherein the negative electrode has a negative electrode active material containing metal particles capable of alloying with Li and graphite particles.

There are provided modified and rounded graphite particles derived from scaly natural graphite particles by modification so as to bring their form close to a spherical form and satisfying all the following requirements (a) to (c): (a) that the degree of circularity should be not less than 0.86; (b) that, upon microscopic observation, the broken-out section should show a cabbage-like appearance with graphite slices taking various directions; and (c) that, upon X ray diffraction, the peak intensity ratio (Ih110/Ih002) between the 002 face (parallel to graphite layers) and 110 face (perpendicular to graphite layers), which serves as an index of the randomness of orientation, should be not less than 0.0050. They retain good qualities of the raw material scaly natural graphite particles and are additionally unique in structure and characteristics. A method of producing such modified particles is also provided. Further provided are secondary cells or batteries in which the modified particles showing good slurry characteristics are used as an electrode material and with which the decrease in discharge capacity is small even at high discharge current values.

The iron-based sintered sliding material comprises: a sintered structure which contains 10-50 wt. % copper and 1-15 wt. % carbon and has been formed by sintering a powder mixture obtained by mixing at least one of an Fe—Cu alloy powder containing copper in an amount which is the solid solubility or larger and is 5-50 wt. %, excluding 50 wt. %, and an Fe—Cu—C alloy powder containing copper in an amount which is the solid solubility or larger and is 5-50 wt. %, excluding 50 wt. %, and containing carbon in an amount of 0-5 wt. %, excluding 0 wt. %, with a graphite powder and at least one of a copper powder and a copper alloy powder; and graphite particles dispersed in the sintered sliding material in an amount of 1-14 wt. % or 3-50 vol. %.

The invention discloses a hard carbon coated lithium ion battery anode material and a preparation method thereof. The anode material is characterized in that the coating material is formed by a heteroatom modifier, a hard carbon precursor material and a soft carbon precursor material, wherein the weight ratio of the heteroatom modifier to the hard carbon precursor to the soft carbon precursor is 1:(2-3.3):(3-9). The preparation method is mainly characterized by comprising the following steps: fully mixing graphite and the coating material, and then carrying out heat treatment on the mixture under the protection of inert atmosphere; preserving the temperature for 0.5-6 hours, and then cooling; and carrying out secondary high-temperature graphitization treatment under the protection of inert atmosphere. The heteroatom modifier can change the structure of the hard carbon in the coating material, and the hard carbon precursor has the characteristics of dissolvability and condensation polymerization with the soft carbon precursor asphalt, thus improving the uniformity and operability of the coated graphite particles; and the ratio of the heteroatom modifier to the hard carbon precursor to the soft carbon precursor has an important effect on the performance of the three. By optimizing the ratio of the heteroatom to the hard carbon precursor to the soft carbon precursor in the coated graphite material, the aims of increasing the capacity of the anode material and improving the cycle performance of the anode material are achieved.

The present invention provides a lithium secondary battery having high-capacity as well as good cycle characteristics. The lithium secondary battery includes a positive electrode comprising a positive active material, a negative electrode comprising a negative active material and an electrolyte. The negative active material includes graphite particles combined to Si particulate. The electrolyte includes a solvent, a polyether modified silicone oil where a linear polyether chain is linked to a polysiloxane chain, and a solute comprising a lithium salt.

The invention discloses a core-shell synergistic flame retardant polyurethane microencapsulation expandable graphite and the application of the expandable graphite in rigid polyurethane foaming plastic. The core-shell synergistic flame retardant polyurethane microencapsulation expandable graphite comprises polyether and/ or polyester polyol, a foaming agent, a foam stabilizer, a catalyst, an organic phosphorus-based flame retardant, a halogen-free intumescent flame retardant, an organic modified nano inorganic filler, core-shell synergistic flame retardant polyurethane microencapsulation expandable graphite, polyisocyanate compound and isocyanate index, wherein the polyisocyanate compound has two or more isocyanate groups; the core-shell synergistic flame retardant polyurethane microencapsulation expandable graphite takes expandable graphite particles as a capsule core and takes cyclodextrin or polyurethane as a capsule shell, wherein the cyclodextrin or polyurethane is formed by crosslinking cyclodextrin/ modified resin and toluene diisocynate. The expandable graphite microcapsule can effectively improve the initial decomposition temperature, the heat stability and the flame retardant effect of a material and remarkably reduces the heat release rate and the total heat release quality during combustion.

A nonaqueous secondary battery includes a working electrode containing graphite particles coated with less crystallized carbon and a nonaqueous electrolyte, which contains at least ethylene carbonate and propylene carbonate.

The invention discloses a carbon-containing material, comprising: graphite particles, which have a 002 plane interval d002 of less than 0.337 nm measured by X-ray wide-angle diffraction method; composite particles, which are arranged and distributed near the surface of the graphite particles, and the composite particles contain Si and C, the particle size of which is smaller than the particle size of graphite; and an amorphous carbon layer, whose in-plane spacing d002 is greater than 0.37 nm, the amorphous carbon layer is a polymer layer and is coated on the graphite particles and composite particles, wherein the said The composite particles include: Si particles, conductive carbon materials arranged and distributed near the surface of the Si particles, and a hard carbon material layer coated on the Si particles and the conductive carbon materials, and the Si particles are composed of crystalline Si phases. Carbonaceous materials have high charge-discharge capacity and improved cycle life characteristics.

The invention discloses a silicon and carbon composite negative electrode material for a lithium ion battery. The material is a three-dimensional composite material of a core-shell structure, and sequentially comprises nanometer silicon/ graphite, a conductive network layer and an organic cracking carbon layer from inside to outside, wherein the nanometer silicon/ graphite uses the graphite as aninner core volume expansion buffer base body; the nanometer silicon particles are embedded in graphite particle gaps or are attached onto the surface of the graphite particles; the conductive networklayer is formed by nanometer conductive agents which penetrate and insert into silicon particle gaps, silicon particle and graphite particle gaps and graphite particle gaps and/or coat the surface ofthe nanometer silicon particles; the organic cracking carbon layer uniformly coat the surface of the silicon nanometer silicon/graphite. The invention also discloses a preparation method of the silicon and carbon negative electrode material. The dispersing agents are used for directly compounding the nanometer silicon slurry, the nanometer conducting agents and organic carbon source; the production process is simple; the operation is easy; the method is suitable for mass production. The material has excellent first time efficiency, circulation performance, rate capability and relatively low volume expansion effects.

The present invention relates to nanostructured materials for use in rechargeable energy storage devices such as lithium batteries, particularly rechargeable secondary lithium batteries, or lithium-ion batteries (LIBs). The present invention includes materials, components, and devices, including nanostructured materials for use as battery active materials, and lithium ion battery (LIB) electrodes comprising such nanostructured materials, as well as manufacturing methods related thereto. Exemplary nanostructured materials include silicon-based nanostructures such as silicon nanowires and coated silicon nanowires, nanostructures disposed on substrates comprising active materials or current collectors such as silicon nanowires disposed on graphite particles or copper electrode plates, and LIB anode composites comprising high-capacity active material nanostructures formed on a porous copper and/or graphite powder substrate.

The present invention is directed to a fire retardant composition, comprising: a primer solution; expandable graphite particles; triethyl phosphate; and aluminum trihydrate, wherein the triethyl phosphate comprises from about 1 wt. % to about 15 wt. % based on the weight of the composition.