Provided is a copper powder manufactured by means of a wet method, wherein the absolute value of the zeta potential of the copper powder is at least 20 mV. The copper powder can be manufactured so as to reduce the burden of the steps of crushing a dry cake and classification, and there is a sufficient reduction in residual secondary particles.

The given invention is related to the field of medicine, namely to experimental research in oncology, and can be used to obtain a pharmaceutical agent for inhibiting the proliferation of HeLa cervical cancer cells. It entails the use of a metal powder obtained in a gaseous medium by means of an electric explosion of a wire made of low-carbon steel carried out with a specific energy of 7-18 kJ/g and a pulse duration of 1.2-2 s. The explosion is carried out inside a reactor that is pre-evacuated to a residual pressure of 10.sup.2 Pa, and then filled with carbon monoxide to a pressure of 10.sup.5 Pa at a gas circulation rate flow of 10 m/s. The products of the explosion deposited in a hopper are passivated in air for at least 48 hours. The resulting powder is extracted and mixed with a solution of the RPMI-1640 nutrient medium with L-glutamine, a pH of 7.2, in the proportion of the mass of the powder to the volume of the specified solution from 1:10 to 2.7:10. The solution is then centrifuged until the phases are separated. The liquid phase is decanted and used as a pharmaceutical agent. The purpose of the given invention is to expand the arsenal of tools for inhibiting the proliferation of tumor cells.

The metal magnetic powder includes Co as a main component, and an average particle size (D50) of 1 nm to 100 nm. An X-ray diffraction chart of the metal magnetic powder has a first peak that appears in a range of a diffraction angle 2? of 41.6?0.3?, and a second peak that appears in a range of a diffraction angle 20? of 47.4?0.3?. When a full width at half maximum of the first peak is set as FW1, and a full width at half maximum of the second peak is set as FW2, a ratio (FW2/FW1) of FW2 to FW1 is 1 to 5.

A metal magnetic powder includes: metal nanoparticles having an average particle size (D50) is 1 nm to 100 nm, and a main phase of hcp-Co; and an additive elements ? including at least one of Fe, Ni, and Cu.

In an example of a method for three-dimensional (3D) printing, one or more dispersions is/are sprayed to form a layer including build material particles and a liquid agent. The liquid agent is evaporated from the layer to form a build material layer, and based on a 3D object model, a binder agent is applied on at least a portion of the build material layer.

In an example of a method for three-dimensional (3D) printing, one or more dispersions is/are sprayed to form a layer including build material particles and a liquid agent. The liquid agent is evaporated from the layer to form a build material layer, and based on a 3D object model, a binder agent is applied on at least a portion of the build material layer.

The present invention discloses a method for preparing nano-copper powder, comprising: (1) providing a dispersion solution, containing copper salt precursor and disperser, the disperser is dissoluble in both water and weak solvents, and is an acrylic modified polyurethane disperser; (2) providing a reducer dispersion solution, containing reducer, the reducer is organic borane; (3) contacting the reducer dispersion solution with the dispersion solution in a condition enough to reduce the copper salt precursor by the reducer into elementary copper; (4) separating copper nano-particles from reaction solution obtained by step (3), and drying separated copper nano-particles by spray drying, so as to obtain the nano-copper powder. The nano-copper powder prepared by the method in accordance with the present invention is dispersible in both water and environment-friendly weak solvents, which can be used to prepare weak solvent-type electrically conductive ink.

The present invention relates to a method for preparing highly active silica magnetic nanoparticles, highly active silica magnetic nanoparticles prepared by the method, and a method of isolating nucleic acid using the highly active silica magnetic nanoparticles. The highly active silica magnetic nanoparticles prepared according to the present invention contain magnetic nanoparticles completely coated with silica, can be used as a reagent for isolating biomaterials, particularly, nucleic acids, and can isolate and purify nucleic acid in a high yield.

The present invention relates to a method for preparing highly active silica magnetic nanoparticles, highly active silica magnetic nanoparticles prepared by the method, and a method of isolating nucleic acid using the highly active silica magnetic nanoparticles. The highly active silica magnetic nanoparticles prepared according to the present invention contain magnetic nanoparticles completely coated with silica, can be used as a reagent for isolating biomaterials, particularly, nucleic acids, and can isolate and purify nucleic acid in a high yield.

A process of forming an oxide dispersion strengthened alloy, comprises distributing an alloy powder on a platform; applying a uniform nanometer-scale metal oxide onto the alloy powder; applying an energy beam onto the alloy powder and the uniform nanometer-scale metal oxide; and forming an oxide dispersion strengthened alloy.