C04B2235/661

Polycrystalline cubic boron nitride and method for manufacturing the same

A polycrystalline cubic boron nitride comprising 98.5% by volume or more of cubic boron nitride, wherein the cubic boron nitride has a dislocation density of more than 8×10.sup.15/m.sup.2, the polycrystalline cubic boron nitride comprises a plurality of crystal grains, and the plurality of crystal grains have a median diameter d50 of an equivalent circle diameter of 0.1 μm or more and 0.5 μm or less.

CARBON FIBER, CARBON COMPOSITE AND FURNACE PURIFICATION BY HYDROGEN REDUCTION FOLLOWED BY THERMAL HEAT TREATMENT
20210381769 · 2021-12-09 · ·

A method of manufacture for a carbon/carbon part including a method to remove contamination from an intermediate product of the carbon/carbon part and furnace utilizing a gaseous reducing agent hydrogen gas to reduce the contaminates, thereby causing the contaminates to transition to a gaseous state at relatively lower temperatures. A method to remove contamination from an intermediate product of the carbon/carbon part and furnace utilizing hydrogen gas to reduce the contaminates, thereby causing the contaminates to transition to a gaseous state at relatively lower temperatures.

DENTAL ZIRCONIA MILL BLANK FOR CUTTING AND MACHINING INCLUDING INDIUM AND YTTRIUM
20220202544 · 2022-06-30 · ·

[Problem]

A technique for imparting high translucency which is similar to an enamel of a natural tooth to a zirconia sintered body, has been required.

[Solution]

To provide a zirconia mill blank for dental cutting and machining, containing, an yttrium compound and an indium compound as stabilizers, wherein, an amount of the yttrium compound is within a range of 3.0 mol % to 6.0 mol % in terms of oxide, an amount of the indium compound is within a range of 0.2 mol % to 3.0 mol % in terms of oxide, and a total amount of the yttrium compound and the indium compound is within a range of 5.5 mol % to 7.0 mol % in terms of oxide.

REFRACTORY OBJECT AND METHOD OF FORMING
20220204408 · 2022-06-30 ·

A refractory object may include a zircon body that is intentionally doped with a dopant including an alkaline earth element and aluminum. The refractory object can have an improved creep deformation rate. In an embodiment, the refractory object can have a creep deformation rate of not greater than about 1.8 E-5 h.sup.−1 at a temperature of 1350° C. and a stress of 2 MPa. In another embodiment, the zircon body may include an amorphous phase including an alkaline earth metal element.

Decorative sheet and decorative material using same

Provided is a decorative sheet comprising a base material layer, a transparent resin layer and a surface protection layer in the presented order, wherein at least one of the base material layer and the transparent resin layer is constituted by a resin composition comprising a resin having an ultraviolet absorption wavelength at least at 270 to 300 nm; absorbance All of the surface protection layer at wavelengths from 270 to 300 nm is 0.6 or more; and absorbance A.sub.12 of the transparent resin layer and the surface protection layer at wavelengths from 270 to 300 nm is 2.7 or more, and wherein the decorative sheet can suppress time-dependent degradation caused by ultraviolet ray, and has excellent weather resistance. Also provided is a decorative material obtained using the decorative sheet.

CERAMIC MATRIX COMPOSITE MANUFACTURING METHOD AND CERAMIC MATRIX COMPOSITE
20220185741 · 2022-06-16 ·

A ceramic matrix composite manufacturing method includes: forming a zirconia-sol containing layer that contains zirconia sol, on fabric having an interface layer formed on a periphery of each of a plurality of ceramic-made fibers; impregnating the fabric having the zirconia-sol containing layer formed, with a polymer as a precursor, to form a body; supplying oxygen to the polymer included in the body; heating the body in an inert gas atmosphere to cause a reaction of the polymer to form a matrix; and heating the body in an oxygen atmosphere to remove the interface layer, after supplying the oxygen and heating the body in the inert gas atmosphere, to generate a ceramic matrix composite in which the matrix is interposed between the fibers.

PROCESS FOR THE PREPARATION OF A POROUS CARBONACEOUS MATERIAL, POROUS CARBONACEOUS MATERIAL, AND A CATALYST MADE OF THE MATERIAL

Known processes for preparing a porous carbonaceous material require lengthy polymerization and washing steps involving solvents or neutralizing agents. The use of high quantities of pore formers leads to a lower carbon yield and higher costs, and use of sulphuric acid leads to sulphur contamination of the final material, but also to corrosion and corrosive by-products and a more complicated handling of the process. In order allows the manufacturing of a porous carbonaceous material with a high pore volume and avoiding the disadvantages of the known methods, a process is provide that comprise the steps of a) providing at least one carbon source and at least one amphiphilic species, b) combining at least the carbon source and the amphiphilic species to obtain a precursor material, c) heating the precursor material to a temperature in the range between 300° C. and 600° C. for at least 15 min so as to obtain a porous carbonaceous material, which is then cooled so as to form the porous carbonaceous material having a modal pore size and a pore volume and a skeleton density.

Garnet materials for Li secondary batteries and methods of making and using garnet materials
11355779 · 2022-06-07 · ·

Set forth herein are garnet material compositions, e.g., lithium-stuffed garnets and lithium-stuffed garnets doped with alumina, which are suitable for use as electrolytes and catholytes in solid state battery applications. Also set forth herein are lithium-stuffed garnet thin films having fine grains therein. Disclosed herein are novel and inventive methods of making and using lithium-stuffed garnets as catholytes, electrolytes and/or anolytes for all solid state lithium rechargeable batteries. Also disclosed herein are novel electrochemical devices which incorporate these garnet catholytes, electrolytes and/or anolytes. Also set forth herein are methods for preparing novel structures, including dense thin (<50 um) free standing membranes of an ionically conducting material for use as a catholyte, electrolyte, and, or, anolyte, in an electrochemical device, a battery component (positive or negative electrode materials), or a complete solid state electrochemical energy storage device. Also, the methods set forth herein disclose novel sintering techniques, e.g., for heating and/or field assisted (FAST) sintering, for solid state energy storage devices and the components thereof.

ZIRCONIA SINTERED BODY AND METHOD FOR PRODUCING SAME
20220162127 · 2022-05-26 · ·

Provided is at least one of a zirconia sintered body and a method for producing the same. The zirconia sintered body can be used in a wide range of applications compared with ceramic joined bodies of the related art that include transparent zirconia. A zirconia sintered body includes a transparent zirconia portion and an opaque zirconia portion, wherein the zirconia sintered body has a biaxial flexural strength of greater than or equal to 300 MPa.

Sputtering Target, Manufacturing Method Therefor, And Manufacturing Method For Magnetic Recording Medium
20230272521 · 2023-08-31 ·

A sputtering target containing silicon nitride (Si.sub.3N.sub.4) with reduced specific resistance of is provided. A sputtering target including Si.sub.3N.sub.4, SiC, MgO and TiCN, wherein a specific resistance of the sputtering target is 10 mΩ.Math.cm or less.