The present invention provides a powder for layer manufacturing including non-hydratable matrix particles, and water-soluble adhesive particles. The powder for layer manufacturing includes, as the water-soluble adhesive particles, polyvinyl alcohol resin particles with a saponification degree of 86.5 mol % to 89.0 mol %, an average degree of polymerization of 400 to 600, a viscosity of a 4 mass % aqueous solution at 20 C. of 4.6 mPa to 5.4 mPa, and an average particle diameter of 20 m to 60 m.

A method for producing a thin-walled metal part with complex geometry includes mixing a metal powder with a polymer binder in order to obtain a composite mixture, producing a flexible composite sheet from the composite mixture, cutting, in the flexible composite sheet, a preform based on a contour of the metal part, applying the preform in a mold having a surface configured with a relief of the metal part, and debinding and sintering the preform in order to obtain the metal part.

A method for producing a thin-walled metal part with complex geometry includes mixing a metal powder with a polymer binder in order to obtain a composite mixture, producing a flexible composite sheet from the composite mixture, cutting, in the flexible composite sheet, a preform based on a contour of the metal part, applying the preform in a mold having a surface configured with a relief of the metal part, and debinding and sintering the preform in order to obtain the metal part.

Anisotropic rare earth magnet powder particles include R.sub.2TM.sub.14B.sub.1-type crystals of a tetragonal compound consisting of one or more rare earth element, B, and one or more transition element, and enveloping layers containing at least Nd and Cu. Surfaces of the R.sub.2TM.sub.14B.sub.1-type crystals are enveloped by the enveloping layers. The particles has an average crystal grain diameter of 0.05 to 1 m. The particles contain, when the whole particles are taken as 100 atomic %, 11.5 to 15 atomic % of total rare earth element (Rt); 5.5 to 8 atomic % of B; and about 0.05 atomic % to about 2 atomic % of Cu. The powder particles have an atomic ratio of Cu, which is a ratio of the total number of Cu atoms to a total number of atoms of Rt, falling within the range of 1 to 6%. The powder particles do not include dysprosium Dy, Tb, Ho and Ga. Coercivity of the magnetic powder is more than 955 kA/m.

There is provided a composite material containing magnetic powder and a polymeric material including the powder in a dispersion state, wherein a content of the magnetic powder with respect to the whole composite material is more than 50% by volume and 75% by volume or less, a saturation magnetic flux density of the composite material is 0.6 T or more, and a relative magnetic permeability of the composite material is more than 20 and is 35 or less. It is preferable that a density ratio of the magnetic powder should be 0.38 or more and 0.65 or less. The density ratio is set to be an apparent density/a true density. Moreover, it is preferable that the magnetic powder should include a plurality of particles constituted of the same material.

Systems and methods for formation of highly reactive alkali dendrites are provided. For example, in some embodiments alkali metals are dissolved in ammonia to form metal electrides after which the ammonia is removed via vacuum to reveal highly activated metal surfaces in the form of crystalline alkali dendrites. The alkali dendrites can mimic powders but have the advantage of being freshly prepared from inexpensive and readily available metal sources. These uniquely activated metals exhibit enhanced reactivity comparatively to similar off the shelf sources of the corresponding metals. For example, the dendrites can have about 100 times greater surface area than conventional metal sources and/or be about 19 times more reactive than powders that serve as the industry standard for the preparation of organometallic compounds. After surface activation, these metals can be used to prepare various organometallic reagents.

A dynamically impacting method comprising simultaneously peening a substrate surface and forming a thin film of metallic glass on the substrate surface for increasing the surface hardness, fatigue resistance, anti-fracture toughness and corrosion resistance of the substrate simultaneously.

Metal nanoparticles and compositions derived therefrom can be used in a number of different applications. Methods for making metal nanoparticles can include providing a first metal salt in a solvent; converting the first metal salt into an insoluble compound that constitutes a plurality of nanoparticle seeds; and after forming the plurality of nanoparticle seeds, reacting a reducing agent with at least a portion of a second metal salt in the presence of at least one surfactant and the plurality of nanoparticle seeds to form a plurality of metal nanoparticles. Each metal nanoparticle can include a metal shell formed around a nucleus derived from a nanoparticle seed, and the metal shell can include a metal from the second metal salt. The methods can be readily scaled to produce bulk quantities of metal nanoparticles.

Example nanoparticles may include an iron-based core, and a shell. The shell may include a non-magnetic, anti-ferromagnetic, or ferrimagnetic material. Example alloy compositions may include an iron-based grain, and a grain boundary. The grain boundary may include a non-magnetic, anti-ferromagnetic, or ferrimagnetic material. Example techniques for forming iron-based core-shell nanoparticles may include depositing a shell on an iron-based core. The depositing may include immersing the iron-based core in a salt composition for a predetermined period of time. The depositing may include milling the iron-based core with a salt composition for a predetermined period of time. Example techniques for treating a composition comprising core-shell nanoparticles may include nitriding the composition.

A method for manufacturing a wrought metallic article from metallic-powder compositions comprises steps of (1) compacting the metallic-powder composition to yield a compact, having a surface, a cross-sectional area, and a relative density of less than 100 percent, (2) reducing the cross-sectional area of the compact via an initial forming pass of a rotary incremental forming process so that the compact has a decreased cross-sectional area, and (3) reducing the decreased cross-sectional area of the compact via a subsequent forming pass of the rotary incremental forming process by a greater percentage than that, by which the cross-sectional area of the compact was reduced during the initial forming pass.