364 results about "Carbon graphite" patented technology

An iron golf club head having a thin (less than 0.12 inches) first section that has an expanded unsupported front face region. The first section including a central portion forming part of a leading edge and wrapping around a sole section of the club, to create an increase the coefficient of restitution of the club head to greater than 0.8. The club head utilizes a rear insert that in addition to providing support for the front face, also allows for the fine tuning of swing weights with no change in geometry or size of the club head. This is accomplished this by the utilization of weight adjustment inserts that impregnate tungsten loaded plastic into sheets of carbon graphite and epoxy. The percentage of tungsten creating a weight range without any size change in the sheets.

Novel composite disc brake rotor assemblies are provided, along with novel and efficient methods for manufacturing them. Preferably, the rotor assemblies comprise annular wear plates formed of particle reinforced aluminum-based metal matrix composite (MMC), ceramic matrix composite (CMC), or of ‘carbon graphite foam.’ The wear plates, made of a first material, are attached to annular surfaces of a central rotor, made of a second material, by fusing bonding layers between the wear plates and the rotor surfaces. The bonding layers are comprised of at least one of a metal alloy having a melting temperature lower than that of either the first or second materials, and a high-temperature adhesive. Preferably, the wear plates comprise projections that are positioned within adjacent receiving recesses in the center rotor. The bonding layers and projections enhance thermal and acoustical transference between the wear plates and the center rotor section. Carbon graphite foam provides for substantially enhanced heat transference. Use of the fusable binding layer, or adhesive provides for an efficient, low cost method of manufacturing for composite disc brake rotor assemblies.

A light-emitting diode reflector assembly having a heat pipe and a reflector body is provided. The assembly further includes a mounting member for mounting a circuit board having an array of light-emitting diodes. The mounting member and reflector body are made from a thermally-conductive polymer composition comprising: i) about 20% to about 80% by weight of a base polymer matrix such as polycarbonate; and ii) about 20% to about 80% by weight of a thermally-conductive material such as carbon graphite.

A fusion cage having a substantially continuous sidewall made from any of various materials including titanium, PEEK, a carbon graphite fiber, or even a combination of these materials. A hollow core defined by the sidewall is typically filled with bone graft in order to form a solid fusion with vertebrae. The sidewall of the cage has upper and lower surfaces, an anterior section, at least two lateral sections each connected to the anterior section, and a posterior section connected to the lateral sections. The sidewall is preferably tapered at one of either a four or eight degree incline from the posterior to the anterior section so as to maintain backbone curvature. A plurality of distinct tool ports provide for anterior, lateral and/or anterolateral insertion of the device. Each tool port is provided with screw insertion orifices.

A thermally actuated shutdown seal provides a shutdown seal usable in a pump having a primary seal assembly positioned circumferentially about a rotating shaft for separating a region of high pressure coolant fluid from the shaft. The shutdown seal includes a two-piece interlocked housing which encompasses carbon graphite ring segments positioned circumferentially about the shaft, a garter spring and a series of compression springs. The replaceable insert with machined recess contains the shutdown seal assembly and is biased axially with a wave spring and held with the annular recess by a closure ring. The seal is designed with coolant fluid flow directly in contact with such ring segments and specially designed paths around the ring segments during normal pump operation. The seal requires a thermally actuated means for moving the two-piece interlocked housing axially into a blocking position within the coolant flow path to shutdown and minimize fluid flow bypassing the ring segments and between the ring segments and the pump shaft, upon occurrence of a process failure in the facility served by the pump and consequent temperature rise of the fluid being pumped.

The invention provides a lightweight brake drum (10) comprising a lightweight, tubular inner member (14) having a reinforcement wrapping retention pattern (e.g., groove) cast in the exterior surface thereof, a length of reinforcement material (e.g., wrapped wire, cable, mesh, fibers, etc.) (16) in communication with a reinforcement retention pattern (e.g., a groove around the inner member) (14), the drum including an outer shell (18). The inner member (14) and the outer shell (18) are made of lightweight materials. Single, or multiple layers of reinforcement material (e.g. wrapping) are applied (e.g., wrapped) around the inner member (14) to support and inhibit expansion of the inner member (14). Because the reinforcement material (16) provides support against expansion, the inner member (14) and the outer shell (18) can be made of lightweight materials. In preferred embodiments, a bonding layer (66) is applied to the exterior surface of the inner member prior to application of the reinforcement material thereon. In preferred embodiments the reinforcement material comprises a low-impedance material such as copper along with another material that has good tensile strength characteristics (e.g., steel, composite fibers, Basalt-fibers, etc.). Preferably, the inner member comprises at least one material selected from the group consisting of a aluminum-based metal matrix composite (MMC) with a particulate reinforcement, ceramic matrix composite (CMC), and carbon graphite foam.

A preparing method of a soft carbon graphite composite anode material is provided. The method includes S1) a step of mixing natural spherical graphite and asphalt, heating and dipping under a preset pressure after fully mixing to allow the asphalt to be softened and to flow into and fill inner pores of the natural spherical graphite, and cooling to obtain an intermediate, and S2) a step of carbonizing the intermediate, crushing and grading to obtain the composite anode material. According to the method, the asphalt is softened at a high temperature, flows into and fills the inner pores of the graphite particles and then carbonization is performed to obtain the composite anode material with excellent cyclic performance. The method is simple in process, low in cost and high in practicality. The soft carbon graphite composite anode material prepared by the method and a lithium ion battery applying the soft carbon graphite composite anode material are also provided.

The invention discloses a preparation method of a soft/hard carbon modified anode material for lithium ion batteries. The method comprises the following steps: (1) carrying out mixed granulation; (2)screening and crushing; (3) mixing; (4) treating at high temperature; (5) screening; (6) modifying; (7) carrying out secondary carbonization. The method is characterized in that a soft carbon precursor and a hard carbon precursor are both used as binding agents, kneading and granulating are carried out at a certain temperature and under other conditions, small graphite particles are polymerized soas to enable the internal structure to be further densified and increase the volume density, high-temperature graphitization is then performed, and asphalt and resin are converted to pyrolytic carbon, so that a soft/hard carbon graphite composite systems is formed; the surface of the modified soft/hard carbon composite anode material is evenly coated with a layer of Ti3SiC2, having good electrical conductivity and stable chemical properties, and a conductive network, so that the improvement of the discharge capacity, discharge efficiency and cycling stability of the graphite anode material isbetter promoted.

The invention relates to a preparation method of a carbon-graphite composite material. The preparation method is characterized in that the carbon-graphite composite material is prepared from the following raw materials in percentage by weight: 1.5-2.5% of carbon black, 5%-8% of graphite with the particle size smaller than or equal to 1mm, 25%-30% of calcined petroleum coke powder with the particle size smaller than or equal to 0.075mm, 15%-20% of calcined petroleum coke with the particle size of 1mm-4mm, 10%-15% of electric calcined anthracite with the particle size of 4mm-10mm, 5%-10% of electric calcined anthracite with the particle size of 10mm-16mm, 5%-15% of calcined pitch coke with the particle size of 10mm-16mm, 18%-20% of coal pitch and short carbon fiber, wherein short carbon fiber is equal to 1%-3% of total weight of the raw materials. The carbon-graphite composite material is prepared by the steps of material preparation, mixed kneading, forming, roasting and graphitization and is excellent in performance, high in breaking strength, relatively good in thermal shock resistance and relatively low in expansion factor; the carbon-graphite composite material does not crack and break and has good stability.

Disclosed is a nm carbon lubricity additive belongs to preparing technique of lubricant material, which is made by the following steps: make use of the effect high temperature electric arc of graphite (nm carbon ball ) pole in the discharge course of the graphite (nm carbon ball ) electric arc discharge method to generate carbon graphite (nm carbon ball ), then assemble them to do surface procession and supersonic dispersion, getting the carbon nm ball with diameter of 5-30 nm. Proved by experiment that after adding into carbon nm lubricity additive, its wear resistance is advanced remarkably, the friction coefficient is decreased by more than 60% and the friction coefficient of surface is notably advanced. Besides, with outstanding biological compatibility, it can be used as lubricity additive of elements of machine, biological and medical equipment. Therefore, the invention has significant practical value and potential application in biological and medical equipment field.

The invention discloses a riser heating and insulating agent, which comprises the following components in percentage by weight: 5 to 35 percent of Al, 10 to 25 percent of AlN, 3 to 20 percent of low-carbon graphite, 5 to 25 percent of magnesia-alumina spinel, 5 to 15 percent of quartz, 10 to 30 percent of ferric oxide powder, 5 to 20 percent of corundum, 5 to 10 percent of organosilicon phlogopite, and 1 to 10 percent of MgO; and the riser heating and insulating agent is prepared by the following processes: crushing, pulverizing, mixing, pelletizing, drying, and the like. The riser heating and insulating agent has double effects of heating and insulating, and has good insulating effect. Because the riser heating and insulating agent has a granular appearance, dust and smoke are not generated in the using process, and the environment is not polluted. Due to the adoption of the low-carbon graphite, castings do not have carburizing phenomenon, and the molten steel is not polluted. The riser heating and insulating agent is particularly applied to open risers of low carbon steel large-scale steel castings and stainless steel castings with the weight of over 80 tons.

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 μm, wherein one or more recesses having a depth of 0.1 to 10 μm 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. The carbon-graphite composite particle of the present invention is produced by performing a thermal CVD step which comprises covering the surface of the above-mentioned graphite particle with a carbon layer.

The invention relates to a copper/graphite compound material and a preparation method thereof. In the compound material, carbon graphite is used as a substrate material, and a tin bronze alloy is used as a dipping metal. The preparation method comprises the following steps: (1) melting the tin bronze alloy to meltwater in a heat treatment furnace, immersing carbon graphite material blocks, and cooling so as to form a copper clad wrap coated by the graphite material blocks; (2) putting the copper clad wrap obtained in the step (1) in a hot isostatic press for hot isostatic press dipping at the temperature of 1100-1300 DEG C under the pressure of 60-80MPa at the atmosphere of argon, carrying out thermal insulation and pressure preservation for 60-120 minutes, and then carrying out belt pressure cooling; and (3) taking out the copper clad wrap obtained in the step (2) and then dissecting the copper clad wrap by using a machining method. The copper/graphite compound material is applied to machinery motive seal or bearings with high parameters (the temperature changes between minus 253 to 350 DEG C and the rotate speed is over 10000 rpm).

Embodiments of the invention provide a lead-acid battery having a positive electrode, a negative electrode, and a separator positioned between the electrodes to electrically insulate the electrodes. Battery includes a nonwoven fiber mat positioned adjacent an electrode. Mat includes a mixture of first glass fibers having diameters between 8 μm to 13 μm and second glass fibers having diameters of at least 6 μm and a silane sizing. An acid resistant binder bonds the glass fibers to form mat. A wetting component is applied to increase the wettability such that mat exhibits an average water wick height of at least 1.0 cm after exposure to water for 10 minutes. A conductive material is disposed on a surface of mat such that when mat is adjacent an electrode, the conductive material contacts the electrode. An electrical resistance of less than 100,000 ohms per square enables electron flow about mat.

The invention relates to a production method for a composite carbon graphite material. The method comprises the following steps: putting pitch coke powder and carbon black in a kneading kettle for mixed kneading, adding melted coal pitch heating and keeping the temperature to obtain carbon powder; putting three carbon fibers in a mixing tank and adding a polyvinyl alcohol aqueous solution to prepare a carbon fiber mixed solution; and adding the carbon powder and the carbon fiber mixed solution to the kneading kettle for mixed kneading, press forming, high-temperature roasting, coal pitch soakage, secondary high-temperature roasting, rough turning, resin soakage, machine processing, secondary resin soakage and grinding into powder. The prepared carbon powder and short fibers are roasted into the composite carbon graphite material which improves the thermal shock resistance, the strength and the impact resistance by 50 percent to 100 percent than a common carbon material and has excellent wearing resistance, thereby being a first-choice carbon graphite material in the aeronautical and astronautic industry and the war industry.

A method for manufacturing a large-specification carbon graphite sealing material matrix comprises the following steps that 1, carbon black and modified pitch are subjected to mixing and pinching, lump making and carbonizing treatment, secondary carbon black powder is obtained, a dispersing agent and modified pitch are mixed and stirred, and modified pitch slurry is obtained; 2, coke powder, graphite powder and the secondary carbon black powder are mixed, mixed powder is obtained, then the mixed powder and the modified pitch slurry are subjected to mixing and pinching, flaking and smashing, flakes are obtained, mesocarbon microbeads and the obtained flakes are mixed, and mixed aggregate is obtained; 3, the mixed aggregate is subjected to isostatic compaction treatment, and green blanks are obtained after demolding; 4, the green blanks are calcined and carbonized, and the carbon graphite sealing material matrix is obtained.The method for manufacturing the large-specification carbon graphite sealing material matrix is short in machining period and low in production cost, and the obtained carbon graphite sealing material matrix has the advantages of being large in specification, high in strength and the like.

The invention provides a grading and separating method for protecting crystalline graphite flakes, and aims to solve the problem of high loss rate of the crystalline graphite flakes. The method comprises the following steps: (1) performing closed circuit grinding on raw ore with a high-pressure grinding roller; (2) grading and separating a ground product obtained in step (1) after 'primary rougherflotation, primary concentration and primary scavenging' flotation; (3) re-grinding and re-separating a coarse-grain low-carbon product to obtain medium-carbon graphite concentrate and middling, screening the medium-carbon graphite concentrate to obtain medium-carbon positive-mesh concentrate and medium-carbon negative-mesh concentrate I; re-grinding and re-separating a medium-grain high-carbon product to obtain high-carbon positive-mesh concentrate and middling; re-grinding and re-separating a fine-grain medium-carbon product to obtain medium-carbon negative-mesh concentrate I; grading the medium-carbon negative-mesh concentrate to obtain high-carbon negative-mech concentrate and medium-carbon negative mesh concentrate II. By adopting the method, differential separation of graphite is realized, and the added value of the graphite concentrate is increased.

The invention discloses a porous carbon-graphene-metal oxide composite material and a preparation method and an application thereof. By the method, the porous carbon-graphene-metal oxide composite material is obtained by searching a substance with a porous material in the natural world, carrying out high-temperature thermal treatment on the substance and graphene oxide to obtain a porous carbon-graphene composite material and compounding a metal oxide on the composite material. By the porous carbon-graphene-metal oxide composite material, the contradictive problems that the artificially prepared porous material is discontinuous in specific surface area and structure and relatively high in internal resistance can be solved; the specific surface area and the conductivity of the porous material are further improved by a graphene material; and the characteristics of high specific surface area and high conductivity are unified on the same composite material. Meanwhile, the capacitive property of the composite material and the strength of the composite material can be further improved by addition of the metal oxide; the composite material can be applied to the aspects of a super capacitor electrode material and the like; the production process is simple and feasible; and the production cost is low.

The invention relates to a preparation method of high-purity graphite. The preparation method of high-purity graphite includes the following steps that 1, medium-carbon or high-carbon graphite is taken, charged into a first-stage graphite extraction device and treated for 0.5-2.0 h at 1000-2000 DEG C; 2, a solid product obtained in the step 1 is charged into a second-stage graphite extraction device and treated for 0.5-1.0 h at 2000-3000 DEG C, and then high-purity graphite is obtained. By means of the preparation method of high-purity graphite, the requirements of a high-temperature method for graphite purification equipment can be lowered, and conditions can be created for industrial promotion of the high-temperature method and industrial production of high-purity graphite with the carbon content larger than 99.99%; meanwhile, the preparation method of high-purity graphite has the advantages of being high in production efficiency, low in energy consumption and the like, is beneficial for large-scale industrial production and has great practical promotion value.