A cubic boron nitride sintered material comprises cubic boron nitride particles and a bonding material, wherein the bonding material comprises at least one first metallic element selected from the group consisting of titanium, zirconium, vanadium, niobium, hafnium, tantalum, chromium, rhenium, molybdenum, and tungsten; cobalt; and aluminum; the cubic boron nitride sintered material has a first interface region sandwiched between an interface between the cubic boron nitride particles and the bonding material, and a first virtual line passing through a point 10 nm apart from the interface to the bonding material side; and when an element that is present at the highest concentration among the first metallic elements in the first interface region is defined as a first element, an atomic concentration of the first element in the first interface region is higher than an atomic concentration of the first element in the bonding material excluding the first interface region.

A cutting element may include a substrate; and an ultrahard layer on the substrate, the substrate and the ultrahard layer defining a non-planar working surface of the cutting element such that the ultrahard layer forms a cutting portion and the substrate is at least laterally adjacent to the ultrahard layer. Another cutting element includes a pointed region having a side surface extending from the pointed region outer perimeter to a peak. An ultrahard material body forms a portion of the pointed region including the peak, and a base region extends a depth from the pointed region outer perimeter. The ultrahard material body has a height to width aspect ratio with the height and width measured between two points of the body having the greatest distance apart along a dimension parallel with a longitudinal axis (i.e., height) along a dimension perpendicular to the longitudinal axis (i.e., width).

The present disclosure provides a powder material that makes it possible to achieve higher flowability than before and to increase the crushing strength of particles. The powder material of the present disclosure has a dendritic structure 1. The dendritic structure 1 has a cemented carbide composition or a cermet composition.

Metallic matrix composites are synthesized by mixing a first reactant, a second reactant and a nucleator compound to obtain a reaction mixture, and heating the reaction mixture to an auto-activation temperature to initiate a self-propagating high-temperature synthesis reaction between the first and second reactants. The metallic matrix composite can include a metallic matrix and an in situ formed reinforcement. The reinforcement can be formed of discrete particles substantially uniformly dispersed within the metallic matrix. Each of the particles can have a reinforcement constituent disposed about a core formed of the nucleator compound.

Metallic matrix composites are synthesized by mixing a first reactant, a second reactant and a nucleator compound to obtain a reaction mixture, and heating the reaction mixture to an auto-activation temperature to initiate a self-propagating high-temperature synthesis reaction between the first and second reactants. The metallic matrix composite can include a metallic matrix and an in situ formed reinforcement. The reinforcement can be formed of discrete particles substantially uniformly dispersed within the metallic matrix. Each of the particles can have a reinforcement constituent disposed about a core formed of the nucleator compound.

The present disclosure relates to a method of making a powder of dense and spherically shaped cemented carbide or cermet granules. The present disclosure also relates to a powder produced by the method and use of said powder in additive manufacturing such as 3D printing by the binder jetting technique. Furthermore, the present disclosure relates to a Hot Isostatic Pressing (HIP) process for manufacturing a product by using said powder.

The present disclosure relates to a method of making a powder of dense and spherically shaped cemented carbide or cermet granules. The present disclosure also relates to a powder produced by the method and use of said powder in additive manufacturing such as 3D printing by the binder jetting technique. Furthermore, the present disclosure relates to a Hot Isostatic Pressing (HIP) process for manufacturing a product by using said powder.

Disclosed is a TiN-based sintered body and a cutting tool made of the TiN-based sintered body, which has 70 to 94 area % of a TiN phase, 1 to 25 area % of a Mo.sub.2C phase, and a remainder including a binder phase. The binder phase contains Fe and Ni whose total area ratio is 5 to 15 area %, and an amount of Ni to a total amount of Fe and Ni is 15 to 35 mass %. When an X-ray diffraction profile is measured in the cross section of the TiN-based sintered body, the diffraction peaks of TiN, Mo.sub.2C and Fe—Ni having an fcc structure are present, but the diffraction peaks of Fe—Ni having a bcc structure, a Fe.sub.3Mo.sub.3C phase, and a Fe.sub.3Mo.sub.3N phase are absent. The lattice constant of the TiN is 4.235 to 4.245 Å, and that of the Fe—Ni having an fcc structure is 3.58 to 3.62 Å.

Disclosed is a TiN-based sintered body and a cutting tool made of the TiN-based sintered body, which has 70 to 94 area % of a TiN phase, 1 to 25 area % of a Mo.sub.2C phase, and a remainder including a binder phase. The binder phase contains Fe and Ni whose total area ratio is 5 to 15 area %, and an amount of Ni to a total amount of Fe and Ni is 15 to 35 mass %. When an X-ray diffraction profile is measured in the cross section of the TiN-based sintered body, the diffraction peaks of TiN, Mo.sub.2C and Fe—Ni having an fcc structure are present, but the diffraction peaks of Fe—Ni having a bcc structure, a Fe.sub.3Mo.sub.3C phase, and a Fe.sub.3Mo.sub.3N phase are absent. The lattice constant of the TiN is 4.235 to 4.245 Å, and that of the Fe—Ni having an fcc structure is 3.58 to 3.62 Å.

Disclosed is a TiN-based sintered body and a cutting tool made of the TiN-based sintered body, which has 70 to 94 area % of a TiN phase, 1 to 25 area % of a Mo.sub.2C phase, and a remainder including a binder phase. The binder phase contains Fe and Ni whose total area ratio is 5 to 15 area %, and an amount of Ni to a total amount of Fe and Ni is 15 to 35 mass %. When an X-ray diffraction profile is measured in the cross section of the TiN-based sintered body, the diffraction peaks of TiN, Mo.sub.2C and Fe—Ni having an fcc structure are present, but the diffraction peaks of Fe—Ni having a bcc structure, a Fe.sub.3Mo.sub.3C phase, and a Fe.sub.3Mo.sub.3N phase are absent. The lattice constant of the TiN is 4.235 to 4.245 Å, and that of the Fe—Ni having an fcc structure is 3.58 to 3.62 Å.