The present invention relates to a method for preparing ferrite/reducing metal composite particles and a method for preparing a high temperature resistant stealth coating based on 3D laser printing, belonging to the technical field of preparation of absorbing coatings. The present invention aims to solve the problems that an existing high-temperature absorbing coating has insufficient coating/matrix bonding force, the microstructure of the coating is difficult to control, and electromagnetic properties cannot be ensured. In the present invention, nano ferrite powder and nano reducing metal powder are prepared into composite particles by a mixing granulation process. In a sealed preparation chamber of a 3D printing device, composite particles are subjected to laser-induced in-situ reaction on the surface of a substrate to prepare a high temperature resistant stealth coating. The present invention is applied to high temperature resistance and stealth of components and prevention and control of electromagnetic pollution.

The present invention relates to a method for preparing ferrite/reducing metal composite particles and a method for preparing a high temperature resistant stealth coating based on 3D laser printing, belonging to the technical field of preparation of absorbing coatings. The present invention aims to solve the problems that an existing high-temperature absorbing coating has insufficient coating/matrix bonding force, the microstructure of the coating is difficult to control, and electromagnetic properties cannot be ensured. In the present invention, nano ferrite powder and nano reducing metal powder are prepared into composite particles by a mixing granulation process. In a sealed preparation chamber of a 3D printing device, composite particles are subjected to laser-induced in-situ reaction on the surface of a substrate to prepare a high temperature resistant stealth coating. The present invention is applied to high temperature resistance and stealth of components and prevention and control of electromagnetic pollution.

A nanoparticle or agglomerate which contains connected multi-walled spherical fullerenes coated in layers of graphite. In different embodiments, the nanoparticles and agglomerates have different combinations of: a high mass fraction compared to other carbon allotropes present, a low concentration of defects, a low concentration of elemental impurities, a high Brunauer, Emmett and Teller (BET) specific surface area, and/or a high electrical conductivity. Methods are provided to produce the nanoparticles and agglomerates at a high production rate without using catalysts.

A method for manufacturing an alloy formed from a boride of a precious metal, the method involving reacting a source of the precious metal with a source of boron in a salt or a mixture of salts in the molten state. The present invention also relates to an alloy formed from a boride of a precious metal, the alloy including crystalline nanoparticles of M.sub.xB.sub.y with M which is a precious metal, distributed in an amorphous matrix of B or in an amorphous matrix of B and of M.sub.zB.sub.a.

Molybdenum composites containing silicon and boron for environmental resistance are combined so as to minimize the silicon solid solution in the molybdenum phase. The composites include ratios of molybdenum, silicon, and boron to form three phase mixtures of molybdenum, A15 (Mo.sub.3Si), and T2 (Mo.sub.5SiB.sub.2) or molybdenum, SiO.sub.2, and T2 (Mo.sub.5SiB.sub.2). Beneficial additives, including manganese and strontium aluminosilicate, are included to improve the composite's properties. Manufacturing processes to produce these composites as either powders or solid parts are included.

Molybdenum composites containing silicon and boron for environmental resistance are combined so as to minimize the silicon solid solution in the molybdenum phase. The composites include ratios of molybdenum, silicon, and boron to form three phase mixtures of molybdenum, A15 (Mo.sub.3Si), and T2 (Mo.sub.5SiB.sub.2) or molybdenum, SiO.sub.2, and T2 (Mo.sub.5SiB.sub.2). Beneficial additives, including manganese and strontium aluminosilicate, are included to improve the composite's properties. Manufacturing processes to produce these composites as either powders or solid parts are included.

A metallic part is disclosed. The part may comprise a functionally graded monolithic structure characterized by a variation between a first material composition of a first structural element and a second material composition of at least one of a second structural element. The first material composition may comprise an alpha-beta titanium alloy. The second material composition may comprise a beta titanium alloy.

A metallic part is disclosed. The part may comprise a functionally graded monolithic structure characterized by a variation between a first material composition of a first structural element and a second material composition of at least one of a second structural element. The first material composition may comprise an alpha-beta titanium alloy. The second material composition may comprise a beta titanium alloy.

A tungsten electrode material contains a tungsten-based material and oxide particles dispersed in the tungsten-based material. The oxide particles are composed of an oxide solid solution in which a Zr oxide and/or an Hf oxide and an oxide of at least one rare earth selected from the group consisting of Sc, Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu are dissolved as a solid solution. A content of the rare-earth oxide with respect to a total amount of the Zr oxide and/or the Hf oxide and the rare-earth oxide is not lower than 66 mol % and not higher than 97 mol %, a content of the oxide solid solution is not lower than 0.5 mass % and not higher than 9 mass %, and the remainder is composed substantially of tungsten.

A tungsten electrode material contains a tungsten-based material and oxide particles dispersed in the tungsten-based material. The oxide particles are composed of an oxide solid solution in which a Zr oxide and/or an Hf oxide and an oxide of at least one rare earth selected from the group consisting of Sc, Y, La, Ce, Pr, Nd, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu are dissolved as a solid solution. A content of the rare-earth oxide with respect to a total amount of the Zr oxide and/or the Hf oxide and the rare-earth oxide is not lower than 66 mol % and not higher than 97 mol %, a content of the oxide solid solution is not lower than 0.5 mass % and not higher than 9 mass %, and the remainder is composed substantially of tungsten.