A method for the preparation of a dense HfC(Si)—HfB.sub.2 composite ceramic. hafnium oxide powders, nano-sized carbon black and silicon hexaboride powders are mixed in a molar ratio of (1-10):(1-20):(1-5) to obtain a powder mixture. The powder mixture is subjected to ball milling, dried and transferred to a graphite mold for spark plasma sintering. In this way, an in-situ carbon-boron reduction reaction and the sintering densification are completed in one step, and the obtained HfC(Si)—HfB.sub.2 composite ceramic has a density of 94.0%-100% and uniformly dispersed grains.

The present invention relates to sintered platelet-like randomly shaped abrasive particles based on alpha alumina having a hardness H.sub.V of at least 20 GPa and a crystal structure with an average crystal size between 100 nm and 300 nm, whereby the abrasive particles comprise a body having a first surface and a second surface opposite to the first surface, both surfaces are separated from each other by a randomly shaped sidewall having a thickness (T) between 20 μm and 500 μm.

The present invention relates to a method for manufacturing a zirconia block for a dental prosthesis having a layered color gradient by a water absorption rate, in which the permeation degree of a coloring solution is controlled by setting a different particle size of powder for each layer of the zirconia block on the basis of the property that the amount of water absorption per hour is differentiated according to the particle size of powder, and as a result, the zirconia block is constituted so as to realize an esthetically excellent resultant product with the same color as natural teeth without carrying out the existing coloring liquid process for zirconia.

The MnZn ferrite material includes principal components and auxiliary components, where the principal components include: 52.5 mol % to 53.8 mol % of Fe.sub.2O.sub.3, 8.8 mol % to 12 mol % of ZnO, and the balance of MnO; the auxiliary components include: 0.35 wt % to 0.5 wt % of Co.sub.2O.sub.3, 0.03 wt % to 0.08 wt % of CaSiO.sub.3, 0.01 wt % to 0.04 wt % of Nb.sub.2O.sub.5, and 0.05 wt % to 0.12 wt % of TiO.sub.2 and RE elemental components; the RE elemental components include one or more from the group consisting of 0 wt % to 0.04 wt % of Gd.sub.2O.sub.3, 0 wt % to 0.02 wt % of HO.sub.2O.sub.3, and 0 wt % to 0.03 wt % of Ce.sub.2O.sub.3; the auxiliary components are all represented by a mass percentage relative to a total mass of the Fe.sub.2O.sub.3, the MnO, and the ZnO.

Embodiments disclosed herein relate to using cobalt (Co) to fine tune the magnetic properties, such as permeability and magnetic loss, of nickel-zinc ferrites to improve the material performance in electronic applications. The method comprises replacing nickel (Ni) with sufficient Co.sup.+2 such that the relaxation peak associated with the Co.sup.+2 substitution and the relaxation peak associated with the nickel to zinc (Ni/Zn) ratio are into near coincidence. When the relaxation peaks overlap, the material permeability can be substantially maximized and magnetic loss substantially minimized. The resulting materials are useful and provide superior performance particularly for devices operating at the 13.56 MHz ISM band.

A method for drying at least one unfired columnar honeycomb formed body comprising a raw material composition containing at least one raw material of ceramics, water and at least one heat-gelling binder, and cells defined by partition walls comprising flow paths from a first end surface to a second end surface. The method comprising drying the honeycomb formed body by passing hot gas satisfying 0.8≤T2/T1≤3.3, where T1 represents a gelation temperature of the binder (° C.) and T2 represents a wet-bulb temperature of the hot gas (° C.) through the flow paths from the first end surface and out the second end surface, while surrounding the honeycomb formed body with a correction mold to correct the shape of the honeycomb formed body during drying.

A porous material includes aggregate particles and a binding material. In the aggregate particles, oxide films containing cristobalite are provided on surfaces of particle bodies that are silicon carbide particles or silicon nitride particles. The binding material contains cordierite and binds the aggregate particles together in a state where pores are provided therein. The mass ratio of the cordierite to the whole of the porous material is in the range of 10 to 40 mass %. The oxide films that exist between the particle bodies and the binding material have a thickness less than or equal to 0.90 μm.

A process for manufacturing a porous abradable coating includes: filling a mold with hollow glass or thermosetting polymer beads and a slurry; and sintering heat treatment to obtain a ceramic layer with pores. A maximum sintering temperature of the green body of the ceramic part is either higher than the melting temperature of the hollow glass beads so that at the end of the sintering heat treatment the hollow glass beads are melted, or higher than the decomposition temperature of the hollow thermosetting polymer beads so that at the end of the sintering heat treatment the hollow thermosetting polymer beads are decomposed.

A low melting-point porous ceramic material, a sintering temperature of the low melting-point porous ceramic material is 680-830° C., a porosity of the low melting-point porous ceramic material is 24-42%, raw materials of the low melting-point porous ceramic material comprise a binder (i.e., a temporary binder) and powder of raw materials.

A ceramic body is provided that is suitable for use in dental applications to provide a natural aesthetic appearance. A colorized ceramic body is formed that has at least one color region and a color gradient region. A ceramic body is formed having at least two color regions and a color gradient that forms a transition region between two color regions. A method for making the colorized ceramic body includes unidirectional infiltration of a coloring composition into the ceramic body.