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3031 results about "Volume fraction" patented technology

In chemistry, the volume fraction φᵢ is defined as the volume of a constituent Vᵢ divided by the volume of all constituents of the mixture V prior to mixing: ϕᵢ=Vᵢ/∑ⱼVⱼ Being dimensionless, its unit is 1; it is expressed as a number, e.g., 0.18. It is the same concept as volume percent (vol%) except that the latter is expressed with a denominator of 100, e.g., 18%. The volume fraction coincides with the volume concentration in ideal solutions where the volumes of the constituents are additive (the volume of the solution is equal to the sum of the volumes of its ingredients).

Hybrid cemented carbide composites

Embodiments of the present invention include hybrid composite materials comprising a cemented carbide dispersed phase and a cemented carbide continuous phase. The contiguity ratio of the dispersed phase of embodiments may be less than or equal to 0.48. The hybrid composite material may have a hardness of the dispersed phase that is greater than the hardness of the continuous phase. For example, in certain embodiments of the hybrid composite material, the hardness of the dispersed phase is greater than or equal to 88 HRA and less than or equal to 95 HRA and the hardness of the continuous phase is greater than or equal to 78 and less than or equal to 91 HRA. Additional embodiments may include hybrid composite materials comprising a first cemented carbide dispersed phase wherein the volume fraction of the dispersed phase is less than 50 volume percent and a second cemented carbide continuous phase, wherein the contiguity ratio of the dispersed phase is less than or equal to 1.5 times the volume fraction of the dispersed phase in the composite material. The present invention also includes a method of making a hybrid cemented carbide composite by blending partially and / or fully sintered granules of the dispersed cemented carbide grade with “green” and / or unsintered granules of the continuous cemented carbide grade to provide a blend. The blend may then be consolidated to form a compact. Finally, the compact may be sintered to form a hybrid cemented carbide.
Owner:KENNAMETAL INC

Hybrid cemented carbide composites

Embodiments of the present invention include hybrid composite materials comprising a cemented carbide dispersed phase and a cemented carbide continuous phase. The contiguity ratio of the dispersed phase of embodiments may be less than or equal to 0.48. The hybrid composite material may have a hardness of the dispersed phase that is greater than the hardness of the continuous phase. For example, in certain embodiments of the hybrid composite material, the hardness of the dispersed phase is greater than or equal to 88 HRA and less than or equal to 95 HRA and the hardness of the continuous phase is greater than or equal to 78 and less than or equal to 91 HRA.Additional embodiments may include hybrid composite materials comprising a first cemented carbide dispersed phase wherein the volume fraction of the dispersed phase is less than 50 volume percent and a second cemented carbide continuous phase, wherein the contiguity ratio of the dispersed phase is less than or equal to 1.5 times the volume fraction of the dispersed phase in the composite material.The present invention also includes a method of making a hybrid cemented carbide composite by blending partially and / or fully sintered granules of the dispersed cemented carbide grade with “green” and / or unsintered granules of the continuous cemented carbide grade to provide a blend. The blend may then be consolidated to form a compact. Finally, the compact may be sintered to form a hybrid cemented carbide.
Owner:KENNAMETAL INC

Reticulated and controlled porosity battery structures

The effective ionic conductivity in a composite structure is believed to decrease rapidly with volume fraction. A system, such as a bipolar device or energy storage device, has structures or components in which the diffusion length or path that electrodes or ions must traverse is minimized and the interfacial area exposed to the ions or electrons is maximized. The device includes components that can be reticulated or has a reticulated interface so that an interface area can be increased. The increased interfacial perimeter increases the available sites for reaction of ionic species. Many different reticulation patterns can be used. The aspect ratio of the reticulated features can be varied. Such bipolar devices can be fabricated by a variety of methods or procedures. A bipolar device having structures of reticulated interface can be tailored for the purposes of controlling and optimizing charge and discharge kinetics. A bipolar device having graded porosity structures can have improved transport properties because the diffusion controlling reaction kinetics can be modified. Graded porosity electrodes can be linearly or nonlinearly graded. A bipolar device having perforated structures also provides improved transport properties by removing tortuosity and reducing diffusion distance.
Owner:MASSACHUSETTS INST OF TECH

Selected processing for non-equilibrium light alloys and products

A new class of light or reactive elements and monophase α′-matrix magnesium- and aluminum-based alloys with superior engineering properties, for the latter being based on a homogeneous solute distribution or a corrosion-resistant and metallic shiny surface withstanding aqueous and saline environments and resulting from the control during synthesis of atomic structure over microstructure to net shape of the final product, said α′-matrix being retained upon conversion into a cast or wrought form. The manufacture of the materials relies on the control of deposition temperature and in-vacuum consolidation during vapor deposition, on maximized heat transfer or casting pressure during all-liquid processing and on controlled friction and shock power during solid state alloying using a mechanical milling technique. The alloy synthesis is followed by extrusion, rolling, forging, drawing and superplastic forming for which the conditions of mechanical working, thermal exposure and time to transfer corresponding metastable α′-matrix phases and microstructure into product form depend on thermal stability and transformation behavior at higher temperatures of said light alloy as well as on the defects inherent to a specific alloy synthesis employed. Alloying additions to the resulting α′-monophase matrix include 0.1 to 40 wt. % metalloids or light rare earth or early transition or simple or heavy rare earth metals or a combination thereof. The eventually more complex light alloys are designed to retain the low density and to improve damage tolerance of corresponding base metals and may include an artificial aging upon thermomechanical processing with or without solid solution heat and quench and annealing treatment for a controlled volume fraction and size of solid state precipitates to reinforce alloy film, layer or bulk and resulting surface qualities. Novel processes are employed to spur production and productivity for the new materials.
Owner:HEHMANN FRANZ

Graphene and carbon nanotube mixed enhanced metal-matrix composite material and preparation method thereof

The invention discloses a graphene and carbon nanotube mixed enhanced metal-matrix composite material and a preparation method thereof. The graphene and carbon nanotube mixed enhanced metal-matrix composite material is characterized in that graphene and a carbon nanotube are mutually connected to constitute an enhanced network in a metal matrix, wherein the graphene is few-layer graphene with 10 layers or less, the radius-thickness ratio of the graphene is larger than 200, and the volume fraction of the graphene is 0.1-1%; and the carbon nanotube is a single-wall, double-wall or multi-wall carbon nanotube, the length-diameter ratio of the carbon nanotube is larger than 20, and the volume fraction of the carbon nanotube is 0.5-5%. Compared with the composite material enhanced only by the carbon nanotube, the graphene and carbon nanotube mixed enhanced metal-matrix composite material disclosed by the invention not only has greatly improved mechanical properties, but also has more excellent electric conduction and heat conduction properties, and is a multi-purpose structure and function integrated material. In addition, the preparation method provided by the invention based on slurry blending and graphene oxide reduction is simple and efficient and is easy for large-scale production.
Owner:SHANGHAI JIAO TONG UNIV
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