A high-purity calcium carbonate sintered body containing less impurities and available for biological and like applications, a production method, a high-purity calcium carbonate porous sintered body containing less impurities and available for biological and like applications, and a production method. A method for producing a high-purity calcium carbonate sintered body includes the steps of: compaction molding calcium carbonate with a purity of 99.7% by mass or more to make a green body; and sintering the green body to produce a calcium carbonate sintered body. A method for producing a high-purity calcium carbonate porous sintered body according to the present invention includes the steps of: preparing a dispersion liquid containing calcium carbonate with a purity of 99.7% by mass or more; adding a foaming agent to the dispersion liquid, followed by stirring until foamy to make a foam; and sintering the foam to produce a calcium carbonate porous sintered body.

A slurry or slip composed of a dispersion medium and a dispersoid including sinterable raw material powder containing a complex oxide powder represented by the following formula (1):
(Tb.sub.1-x-yR.sub.xSc.sub.y).sub.3(Al.sub.1-zSc.sub.z).sub.5O.sub.12  (1)
wherein R is yttrium and/or lutetium, 0.05≤x<0.45, 0<y<0.1, 0.5<1-x-y<0.95, and 0.004<z<0.2 is prepared; the slurry or slip is subsequently enclosed in a mold container to be subjected to solid-liquid separation by centrifugal casting to mold a cast compact; the cast compact is dried thereafter; a dried compact is degreased; a degreased compact is sintered thereafter; and a sintered body is further subjected to a hot isostatic pressing treatment to obtain the transparent ceramic material composed of the sintered body of garnet-type rare earth complex oxide represented by the formula (1).

Provided is a ferrite sintered magnet including a ferrite phase having a magnetoplumbite-type crystal structure. x, y, and m satisfy the following Equations (1), (2), and (3) when composition of the ferrite sintered magnet is represented by R.sub.1-xA.sub.xFe.sub.m-yCo.sub.y, where R denotes at least one kind of element selected from rare earth elements including Y and A denotes Ca or Ca and elements including at least one kind selected from Sr or Ba. The content of B in the ferrite sintered magnet is from 0.1% to 0.6% by mass in terms of B.sub.2O.sub.3.

0.2≤x≤0.8  (1)

0.1≤y≤0.65  (2)

3≤m≤14  (3)

A method of making a formed ceramic abrasive particle is presented that includes molding a dispersion of a ceramic abrasive particle precursor mixture. The method also includes drying the molded dispersion to form a ceramic abrasive particle particle precursor. The method also includes calcining the ceramic abrasive particle precursor. The method also includes sintering the ceramic abrasive particle precursor to form the formed ceramic abrasive particle. The method also includes impregnating the ceramic abrasive particle precusor with a mixture. The mixture includes one or more of a first group consisting of: an oxide of yttrium, praseodymium, samarium, ytterbium, neodymium, lanthanum, gadolinium, dysprosium, and erbium or one or more of a second group consisting of: oxide of iron, magnesium, zinc, silicon, cobalt, nickel, zirconium, hafnium, chromium, cerium, titanium. Impregnating the ceramic abrasive particle precursor occurs after drying, calcining or sintering.

An abrasive particle having a body including a first major surface, a second major surface opposite the first major surface, and a side surface extending between the first major surface and the second major surface, such that a majority of the side surface comprises a plurality of microridges.

The present disclosure discloses a nanoporous ceramic for an atomization core, and a preparation method thereof. The nanoporous ceramic includes: nano-silica 1 to 60 parts, a ceramic powder 10 to 80 parts, a pore-forming agent 1 to 50 parts, and a sintering additive 1 to 40 parts. The preparation method includes: (1) weighing raw materials, and mixing and ball-milling the raw materials in a ball mill; (2) bake-drying the ball-milled raw materials to obtain a dried mixed powder; (3) adding the dried mixed powder to molten paraffin under stirring, and continuously stirring a resulting mixture to obtain a paraffin slurry; (4) injecting the paraffin slurry into a mold, cooling the mold for forming, and performing demolding to obtain a paraffin mold; (5) preheating the paraffin mold for paraffin removal to obtain a paraffin-removed sample; and (6) sintering and cooling the paraffin-removed sample to obtain the nanoporous ceramic.

The present invention relates to a green body, a pre-ceramic body and a ceramic body based on metal oxide particles, in particular zirconium oxide. The present invention also relates to the method of producing said materials and to the use thereof, in particular in the field of dentistry.

Method for manufacturing a CMC, i.e. ceramic matrix composite material, part provided with at least one cutout, as well as to such a CMC part provided with at least one cutout, the method comprising the following steps: providing (E1) a fibrous reinforcement (10), forming (E2′) a cavity in a portion of the fibrous reinforcement (10), injecting (E3) a slip comprising at least a ceramic powder and a solvent, the slip being injected so as to impregnate the fibrous reinforcement (10′) and to fill the cavity of the fibrous reinforcement (10′), drying (E4) the obtained assembly, carrying out a densification (E6) by infiltration of a liquid densification material and solidification of said densification material, machining (E7) at least one cutout in the obtained blank (30) within the volume corresponding to the cavity of the fibrous reinforcement (10).

A cubic boron nitride (cBN)-based composite including about 30-65 vol. % cBN, about 15-45 vol. % titanium (Ti)-containing binders, about 2-20 vol. % zirconium dioxide (ZrO.sub.2), about 3-15 vol. % cobalt-tungsten-borides (Co.sub.xW.sub.yB.sub.z), and about 2-15 vol. % aluminum oxide (Al.sub.2O.sub.3).

A cubic boron nitride (cBN)-based composite including about 30-65 vol. % cBN, about 3-30 vol. % zirconium (Zr)-containing compounds, about 0-10 vol. % cobalt-tungsten-borides (Co.sub.xW.sub.yB.sub.z), about 2-30 vol. % aluminum oxide (Al.sub.2O.sub.3), about 0.5-10 vol. % tungsten borides, and less than or equal to about 5 vol. % aluminum nitride (AlN).