C04B2235/386

DRILLING TOOLS MADE OF WURTZITE BORON NITRIDE (W-BN)

Systems and methods include a computer-implemented method can be used to make drilling tools from new wurtzite boron nitride (w-BN) superhard material. An ultra-high-pressure, high-temperature operation is performed on pure w-BN powder to synthesize w-BN and cubic boron nitride (c-BN) compact having a first size greater than particles of the pure w-BN powder. The ultra-high-pressure, high-temperature operation includes pressurizing the w-BN powder to a pressure of approximately 20 Gigapascal, heating the w-BN powder at a heating rate of 100° C./minute and cooling the w-BN powder at a cooling rate of 50° C./minute. The compact is cut to a second size smaller than the first size using laser cutting tools. The cut compact is bonded metallurgically, mechanically, or both metallurgically and mechanically onto a tool substrate to form the drilling tool.

CUBIC BORON NITRIDE SINTERED MATERIAL

A cubic boron nitride sintered material includes: 20 to 80 volume % of cBN grains; and 20 to 80 volume % of a binder phase, wherein the binder phase includes first binder grains and second binder grains, in each of the first binder grains, a ratio of the number of atoms of the first metal element to a total of the number of atoms of the titanium and the first metal element is more than or equal to 0.01% and less than 10%, in each of the second binder grains, the ratio is more than or equal to 10% and less than or equal to 80%, and an average grain size of the second binder grains is more than or equal to 0.2 μm and less than or equal to 1 μm.

CUBIC BORON NITRIDE SINTERED MATERIAL AND METHOD OF PRODUCING SAME
20220204411 · 2022-06-30 ·

A cubic boron nitride sintered material includes: more than or equal to 20 volume % and less than 80 volume % of cubic boron nitride grains; and more than 20 volume % and less than or equal to 80 volume % of a binder phase, and when a carbon content is measured from a cubic boron nitride grain into the binder phase in a direction perpendicular to an interface between the cubic boron nitride grain and the binder phase using TEM-EDX, a first region having a carbon content larger than an average value of a carbon content of the binder phase exists, the interface exists in the first region, and a length of the first region is more than or equal to 0.1 nm and less than or equal to 10 nm.

CUBIC BORON NITRIDE SINTERED MATERIAL

A cubic boron nitride sintered material includes: 20 to 80 volume % of cBN grains; and 20 to 80 volume % of a binder phase, wherein the binder phase includes first binder grains and second binder grains, in each of the first binder grains, a ratio of the number of atoms of the first metal element to a total of the number of atoms of the titanium and the number of atoms of the first metal element is more than or equal to 0.01% and less than 10%, in each of the second binder grains, this ratio is more than or equal to 10% and less than or equal to 80%, and in an X-ray diffraction spectrum of the cubic boron nitride sintered material, one or both of conditions 1 and 2 are satisfied.

Dense sintered product
11370710 · 2022-06-28 · ·

Sintered product having a chemical analysis such that, in mass percentages: SiO.sub.2 content is greater than 0.2% and less than 2%, and CaO content is greater than 0.1% and less than 1.5%, and MgO content is less than 0.3%, and alumina and other elements being the complement at 100%, the content of other elements being less than 1.5%, having a relative density greater than 90%, comprising, for more than 90% of its volume, a stack of ceramic platelets (10) laid flat, all of said platelets having an average thickness less than 3 μm, more than 95% by number of said platelets each containing more than 95% by mass of alumina, having a width (l) greater than 81 mm.

COMPOSITE, METHOD FOR PRODUCING COMPOSITE, LAMINATE, AND METHOD FOR PRODUCING LAMINATE

The present disclosure provides a composite including a nitride sintered body having a porous structure and a semi-cured product of a heat-curable composition impregnated into the nitride sintered body, wherein a dielectric breakdown voltage obtainable after disposing the composite between adherends, heating and pressurizing the composite for 5 minutes under the conditions of 200° C. and 10 MPa, and further heating the composite for 2 hours under the conditions of 200° C. and atmospheric pressure, is greater than 5 kV.

HYBRID WOVEN FIBER PREFORM-REINFORCED COMPOSITE MATERIAL AND PREPARATION METHOD THEREOF

The present disclosure discloses a hybrid woven fiber preform-reinforced composite material, including a fiber preform, a composite material interface and a matrix, where the fiber preform is a three-dimensional fabric hybrid woven by 2-5 high-performance inorganic fibers, and the matrix is selected from the group consisting of resin, light alloy, carbon and ceramic. A preparation method of the composite material includes: preparing ceramic slurry, fiber bundle impregnation treatment, fiber weaving, molding of three-dimensional overall structure preform, preform heat treatment, preparing interface and preparing matrix. The present disclosure improves the weaving performance of inorganic rigid fibers, and the prepared hybrid woven fiber preform-reinforced composite material has desirable integrity, high interlayer bonding strength, and is not easy to layer. Meanwhile, the present disclosure realizes the functions of wave transmission, wave-absorbing, high-temperature structural material, thermal insulation and thermal prevention through the combination of hybrid woven fibers.

CONTINUOUS ELECTROPHORETIC DEPOSITION MODIFIED CARBON FIBER REINFORCED MULTI-MATRIX COMPOSITE AND PREPARATION METHOD THEREOF

The present disclosure discloses a continuous electrophoretic deposition modified carbon fiber reinforced multi-matrix composite and a preparation method thereof, composing of a carbon fiber with a volume fraction of 30-55%, an inorganic powder with a volume fraction of 3-25% and a matrix with a volume fraction of 20-67%, wherein the inorganic powder is wrapped on the surface of the carbon fiber filament or embedded in the carbon fiber bundle, and the concentration gradually decreases from the fiber filament to the surface of the fiber bundle. The preparation method of the composite is as follows: (1) pretreating the carbon fibers; (2) preparing a slurry of the inorganic powder; (3) widening the pretreated carbon fiber to form a carbon fiber strip, and then carrying out electrophoretic deposition on the inorganic powders; (4) preparing a preform from the deposited carbon fibers; and (5) compounding a matrix in the preform.

Method for producing a particulate carrier material, which is sheathed in a graphene-containing material, and a ceramic component, and ceramic component

The invention relates to a sliding member having a first sliding surface, wherein the first sliding surface (29) comprises a particulate support material (6) and a graphene-containing material (7), wherein the particulate support material (6) is at least partially coated with the graphene-containing material (7), and wherein a material bond (14) is present between the particulate support material (6) and the graphene-containing material (7).

Indirect additive manufacturing process for producing SiC—B4C—Si composites

A method for indirect additive manufacturing of an object constructed of boron carbide, silicon carbide, and free silicon, comprising: (i) producing a porous preform constructed of boron carbide and silicon carbide by an indirect ceramic additive manufacturing (ICAM) process in which particles of a powder mixture become bonded together with an organic binder, wherein the powder mixture comprises: a) boron carbide particles, and b) silicon carbide particles, wherein at least 80 vol % of the silicon carbide particles are larger than the boron carbide particles; and wherein the boron carbide and silicon carbide particles are each included in an amount of 40-60 wt. % of the powder mixture, provided that the foregoing amounts sum to at least 95 wt. %; (ii) subjecting the porous preform to a temperature of 500-900° C. to volatilize the organic binder; and (iii) infiltrating molten silicon into pores of the porous preform to produce the object.