The invention relates to a method for preparing high-melting-point metal powder through multi-stage deep reduction, and belongs to the technical field of preparation of powder. The method includes the following steps of mixing dried high-melting-point metal oxide powder with magnesium powder and performing a self-propagating reaction, placing an intermediate product into a closed reaction kettle, leaching the intermediate product with hydrochloric acid as a leaching solution so as to obtain a low-valence oxide Me.sub.xO precursor of the low-valence high-melting-point metal; uniformly mixing the precursor with calcium powder, pressing the mixture, placing the pressed mixture into a vacuum reduction furnace, heating the vacuum reduction furnace to 700-1200° C., performing deep reduction for 1-6 h, leaching a deep reduction product with hydrochloric acid as a leaching solution and performing treatment, so as to obtain the high-melting-point metal powder.

This invention relates to a method for controlling exothermic reactions between metal chlorides of Zn, V, Cr, Co, Sn, Ag, Ta, Ni, Fe, Nb Cu, Pt, W, Pd, and Mo, and Al and the use of the method for preparation of metallic alloys and compounds based on base metals Zn, V, Cr, Co, Sn, Ag, Ta, Ni, Fe, Nb Cu, Pt, W, Pd, and Mo. The method provides for a mixture of precursor chemicals including at least one solid base metal chloride to be mixed and reacted exothermically with a control powder based on Zn, V, Cr, Co, Sn, Ag, Ta, Ni, Fe, Nb Cu, Pt, W, Pd, and Mo and then reacting the resulting intermediates with an Al scavenger. Reduction is carried out in a controlled manner to regulate reaction rates and prevent excessive rise in the temperature of the reactants and the reaction products.

The invention relates to a method for preparing high-melting-point metal powder through multi-stage deep reduction, and belongs to the technical field of preparation of powder. The method includes the following steps of mixing dried high-melting-point metal oxide powder with magnesium powder and performing a self-propagating reaction, placing an intermediate product into a closed reaction kettle, leaching the intermediate product with hydrochloric acid as a leaching solution so as to obtain a low-valence oxide Me.sub.xO precursor of the low-valence high-melting-point metal; uniformly mixing the precursor with calcium powder, pressing the mixture, placing the pressed mixture into a vacuum reduction furnace, heating the vacuum reduction furnace to 700-1200 C., performing deep reduction for 1-6 h, leaching a deep reduction product with hydrochloric acid as a leaching solution and performing treatment, so as to obtain the high-melting-point metal powder.

This invention relates to a method for controlling exothermic reactions between metal chlorides of Zn, V, Cr, Co, Sn, Ag, Ta, Ni, Fe, Nb Cu, Pt, W, Pd, and Mo, and Al and the use of the method for preparation of metallic alloys and compounds based on base metals Zn, V, Cr, Co, Sn, Ag, Ta, Ni, Fe, Nb Cu, Pt, W, Pd, and Mo. The method provides for a mixture of precursor chemicals including at least one solid base metal chloride to be mixed and reacted exothermically with a control powder based on Zn, V, Cr, Co, Sn, Ag, Ta, Ni, Fe, Nb Cu, Pt, W, Pd, and Mo and then reacting the resulting intermediates with an Al scavenger. Reduction is carried out in a controlled manner to regulate reaction rates and prevent excessive rise in the temperature of the reactants and the reaction products.

The invention provides a method for the production of a metal, the method comprising the steps of mixing an oxide of the metal with a reducing agent comprising a Group II metal or a hydride thereof in the presence of water and/or an organic solvent, heating the mixture of oxide and reducing agent, leaching the resulting material with water; and washing the leached material with a dilute aqueous acid. Typically, the metal is a transition or rare earth metal, the oxide of the metal is an oxide of a transition or rare earth metal, and the reducing agent is selected from calcium or magnesium or the hydrides of calcium and magnesium. The metal is generally obtained at a purity of around 98.5-99.1%, and the method is much quicker than the methods of the prior art and has a much lower carbon footprint, thereby providing an option which is more sustainable, environmentally friendly, and accommodative for industries. Particularly good results are observed in the production of transition metals such as titanium, tantalum and niobium.

The invention provides a method for the production of a metal, the method comprising the steps of mixing an oxide of the metal with a reducing agent comprising a Group II metal or a hydride thereof in the presence of water and/or an organic solvent, heating the mixture of oxide and reducing agent, leaching the resulting material with water; and washing the leached material with a dilute aqueous acid. Typically, the metal is a transition or rare earth metal, the oxide of the metal is an oxide of a transition or rare earth metal, and the reducing agent is selected from calcium or magnesium or the hydrides of calcium and magnesium. The metal is generally obtained at a purity of around 98.5-99.1%, and the method is much quicker than the methods of the prior art and has a much lower carbon footprint, thereby providing an option which is more sustainable, environmentally friendly, and accommodative for industries. Particularly good results are observed in the production of transition metals such as titanium, tantalum and niobium.

A niobium or niobium alloy which contains pure or substantially pure niobium and at least one metal element selected from the group consisting of Ru, Rh, Pd, Os, Ir, Pt, Mo, W and Re to form a niobium alloy that is resistant to aqueous corrosion. The invention also relates to the process of preparing the niobium alloy.