A sacrificial ceramic CO.sub.2 sequestration architectural product comprising a sintered/heat-treated mixture that comprises: one or more reactive solid phases, wherein each reactive solid phase comprises one or more weathering materials capable of enhanced mineralization, and one or more particle-bridging phases that bridge the one or more reactive solid phases, and an open porosity that is in a range from about 15 vol% to about 30 vol%.

A cubic boron nitride sintered material includes: 0 to 85 volume % of cubic boron nitride grains; and a binder phase, wherein the binder phase includes at least one selected from a group consisting of one or more first compounds and a solid solution originated from the first compounds, the cubic boron nitride grains include, on number basis, more than or equal to 50% of cubic boron nitride grains each having an equivalent circle diameter of more than 0.5 μm, and includes, on number basis, less than or equal to 50% of cubic boron nitride grains each having an equivalent circle diameter of more than 2 μm, and when a mass of the cubic boron nitride grains is assumed as 100 mass %, a total content of lithium, magnesium, calcium, strontium, beryllium, and barium in the cubic boron nitride grains is less than 0.001 mass %.

A cubic boron nitride sintered material includes: to 98 volume % of cubic boron nitride grains; and a binder phase, wherein the binder phase includes at least one selected from a group consisting of one or more first compounds and a solid solution originated from the first compounds, the cubic boron nitride grains include, on number basis, more than or equal to 50% of cubic boron nitride grains each having an equivalent circle diameter of more than 0.5 μm, and includes, on number basis, less than or equal to 50% of cubic boron nitride grains each having an equivalent circle diameter of more than 2 μm, and when a mass of the cubic boron nitride grains is assumed as 100 mass %, a total content of lithium, magnesium, calcium, strontium, beryllium, and barium in the cubic boron nitride grains is less than 0.001 mass %.

Polycrystalline cubic boron nitride, PCBN, material and methods of making PCBN. A method includes providing a matrix precursor powder comprising particles having an average particle size no greater than 250 nm, providing a cubic boron nitride, cBN, powder comprising particles of cBN having an average particle size of at least 0.2 intimately mixing the matrix precursor powder and the cBN powder, and sintering the intimately mixed powders at a temperature of at least 1100° C. and a pressure of at least 3.5 GPa to form the PCBN material comprising particles of cubic boron nitride, cBN dispersed in a matrix material.

The present invention provides a ferrite sintered magnet comprising ferrite crystal grains having a hexagonal structure, wherein the ferrite sintered magnet comprises metallic elements at an atomic ratio represented by formula (1). In formula (1), R is at least one element selected from the group consisting of Bi and rare-earth elements, and R comprises at least La. In formula (1), w, x, z and m satisfy formulae (2) to (5). The above-mentioned ferrite sintered magnet further has a coefficient of variation of a size of the crystal grains in a section parallel to a c axis of less than 45%.
Ca.sub.1-w-xR.sub.wSr.sub.xFe.sub.zCo.sub.m  (1)
0.360≤w≤0.420  (2)
0.110≤x≤0.173  (3)
8.51≤z≤9.71  (4)
0.208≤m≤0.269  (5)

Polycrystalline cubic boron nitride, PCBN, material and methods of making PCBN. A method includes providing a matrix precursor powder comprising particles having an average particle size no greater than 250 nm, providing a cubic boron nitride, cBN, powder comprising particles of cBN having an average particle size of at least 0.2 μm, intimately mixing the matrix precursor powder and the cBN powder, and sintering the intimately mixed powders at a temperature of at least 1100° C. and a pressure of at least 3.5 GPa to form the PCBN material comprising particles of cubic boron nitride, cBN dispersed in a matrix material.

A heat-dissipating member includes aluminum oxide ceramics that includes crystal particles of aluminum oxide. The aluminum oxide ceramics includes 98 mass % or higher of aluminum in terms of Al.sub.2O.sub.3 with respect to 100 mass % of all constituents. The crystal particles have an average equivalent circle diameter of 1.6 μm or more and 2.4 μm or less. An equivalent circle diameter cumulative distribution curve of the crystal particles has a first diameter at 10 cumulative percent and a second diameter at 90 cumulative percent that is different from the first diameter by 2.1 μm or more and 4.2 μm or less.

A method of making a ceramic matrix composite component includes forming a ceramic matrix composite component by infiltrating an array of ceramic-based reinforcements with a ceramic-based matrix, applying filler particles to a surface of the ceramic matrix composite component such that the filler particles fill in gaps between adjacent ones of the ceramic-based reinforcements, and infiltrating the filler particles with a filler matrix. A ceramic matrix composite component is also disclosed.

The disclosure relates to sintered ceramic grains comprising 3-55 wt. % alumina, 40-95 wt. % zirconia and 1-30 wt. % of one or more other inorganic components. The invention further relates to a method for preparing ceramic grains according to the invention, comprising: making a slurry comprising alumina, zirconia; making droplets of the slurry; introducing the droplets in a liquid gelling-reaction medium wherein the droplets are gellified; drying the gellified deformed droplets.

A sintered bead and an associated method. The sintered bead has the following chemical composition, as mass percentages on the basis of the oxides: ZrO.sub.2+HfO.sub.2+Y.sub.2O.sub.3+CeO.sub.2: remainder to 100%; 0%≤Al.sub.2O.sub.3≤1.5%; CaO≤2%; oxides other than ZrO.sub.2, HfO.sub.2, Y.sub.2O.sub.3, CeO.sub.2, Al.sub.2O.sub.3 and CaO: ≤5%. The contents of Y.sub.2O.sub.3 and CeO.sub.2, as molar percentages on the basis of the sum of ZrO.sub.2, HfO.sub.2, Y.sub.2O.sub.3 and CeO.sub.2, being such that 1.8%≤Y.sub.2O.sub.3≤2.5% and 0.1%≤CeO.sub.2≤0.9%. The sintered bead has following crystalline phases, as mass percentages on the basis of the crystalline phases and for a total of 100%: stabilized zirconia: remainder to 100%; monoclinic zirconia: ≤10%; crystalline phases other than stabilized zirconia and monoclinic zirconia: <7%.