Patent classifications
B22F9/22
METHODS FOR THE PRODUCTION OF FINE METAL POWDERS
Methods for the manufacture of fine metal powders from metal-containing ammonium compounds such as ammonium oxalate metal salts. The method includes decomposing particulates of the ammonium oxalate metal salt by heating to a decomposition temperature in the presence of a dilute hydrogen gas to decompose the ammonium oxalate compound, and form a fine metal powder by heating to a higher refining temperature to remove contaminants from the fine metal powder. The method may include the conversion of a non-oxalate metal compound to a hydrated metal oxalate and the dehydration of the hydrated metal oxalate before decomposition to the metal. The method is applicable to the production of a wide variety of metals of high purity and fine particle size.
METHODS FOR THE PRODUCTION OF FINE METAL POWDERS
Methods for the manufacture of fine metal powders from metal-containing ammonium compounds such as ammonium oxalate metal salts. The method includes decomposing particulates of the ammonium oxalate metal salt by heating to a decomposition temperature in the presence of a dilute hydrogen gas to decompose the ammonium oxalate compound, and form a fine metal powder by heating to a higher refining temperature to remove contaminants from the fine metal powder. The method may include the conversion of a non-oxalate metal compound to a hydrated metal oxalate and the dehydration of the hydrated metal oxalate before decomposition to the metal. The method is applicable to the production of a wide variety of metals of high purity and fine particle size.
METHODS FOR FABRICATING REFRACTORY COMPLEX CONCENTRATED ALLOYS AND COMPOSITES CONTAINING SUCH ALLOYS, AND BODIES CONTAINING THE SAME
Methods for producing final bodies that contain a fine-grained refractory complex concentrated alloy (RCCA), as well as RCCAs, intermediate materials and final bodies containing the RCCAs, and high-temperature devices formed by such final bodies. Such a method includes providing a precursor with one or more precursor compounds containing elements of an RCCA, reducing the precursor compounds in the precursor via reaction with a reducing agent so as to generate the RCCA and a compound comprising a product of the reaction between the reducing agent and the precursor compounds, generating a solid material that contains at least the RCCA, forming with the solid material a porous intermediate body, and consolidating the porous intermediate body so as to partially or completely remove the pore volume from the porous intermediate body, and in doing so yield either a denser final body or a denser film.
METHODS FOR FABRICATING REFRACTORY COMPLEX CONCENTRATED ALLOYS AND COMPOSITES CONTAINING SUCH ALLOYS, AND BODIES CONTAINING THE SAME
Methods for producing final bodies that contain a fine-grained refractory complex concentrated alloy (RCCA), as well as RCCAs, intermediate materials and final bodies containing the RCCAs, and high-temperature devices formed by such final bodies. Such a method includes providing a precursor with one or more precursor compounds containing elements of an RCCA, reducing the precursor compounds in the precursor via reaction with a reducing agent so as to generate the RCCA and a compound comprising a product of the reaction between the reducing agent and the precursor compounds, generating a solid material that contains at least the RCCA, forming with the solid material a porous intermediate body, and consolidating the porous intermediate body so as to partially or completely remove the pore volume from the porous intermediate body, and in doing so yield either a denser final body or a denser film.
Process for production of particulate ruthenium
Process for the production of particulate ruthenium with a purity of 99.99 wt. % and a specific surface area of 0.2-0.5 m.sup.2/g, comprising: (1) providing a hydrochloric solution prepared by dissolving RuO.sub.4 in hydrochloric acid and has a content of ruthenium in the form of dissolved ruthenium species of 15-22 wt. %; (2) providing an aqueous solution with an ammonium chloride content of 200-600 g/litre; (3) forming a reaction mixture by dosing the hydrochloric solution provided in step (1) to the aqueous solution provided in step (2) at a molar ratio of 1 mol ruthenium: 3-6 mol ammonium chloride, at a temperature of 55-90 C. over the course of 0.2-5 hours and while adjusting and maintaining a pH of 0.6 to 0; (4) separating solid material formed during step (3) from the hydrochloric reaction mixture; and (5) calcinating the solid material separated in step (4) at an object temperature of 350-1,000 C.
Process for production of particulate ruthenium
Process for the production of particulate ruthenium with a purity of 99.99 wt. % and a specific surface area of 0.2-0.5 m.sup.2/g, comprising: (1) providing a hydrochloric solution prepared by dissolving RuO.sub.4 in hydrochloric acid and has a content of ruthenium in the form of dissolved ruthenium species of 15-22 wt. %; (2) providing an aqueous solution with an ammonium chloride content of 200-600 g/litre; (3) forming a reaction mixture by dosing the hydrochloric solution provided in step (1) to the aqueous solution provided in step (2) at a molar ratio of 1 mol ruthenium: 3-6 mol ammonium chloride, at a temperature of 55-90 C. over the course of 0.2-5 hours and while adjusting and maintaining a pH of 0.6 to 0; (4) separating solid material formed during step (3) from the hydrochloric reaction mixture; and (5) calcinating the solid material separated in step (4) at an object temperature of 350-1,000 C.
Process for production of particulate ruthenium
Process for the production of particulate ruthenium with a purity of 99.99 wt. % and a specific surface area of 0.2-0.5 m.sup.2/g, comprising: (1) providing a hydrochloric solution prepared by dissolving RuO.sub.4 in hydrochloric acid and has a content of ruthenium in the form of dissolved ruthenium species of 15-22 wt. %; (2) providing an aqueous solution with an ammonium chloride content of 200-600 g/litre; (3) forming a reaction mixture by dosing the hydrochloric solution provided in step (1) to the aqueous solution provided in step (2) at a molar ratio of 1 mol ruthenium: 3-6 mol ammonium chloride, at a temperature of 55-90 C. over the course of 0.2-5 hours and while adjusting and maintaining a pH of 0.6 to 0; (4) separating solid material formed during step (3) from the hydrochloric reaction mixture; and (5) calcinating the solid material separated in step (4) at an object temperature of 350-1,000 C.
Methods using high surface area per volume reactive particulate
A method of processing finely divided reactive particulates (R.sub.Particulate) and forming a product comprising: providing a composite material comprising finely divided reactive particulates (R.sub.Particulate) dispersed in a protective matrix; at least partially exposing the finely divided reactive particulates (R.sub.Particulate); and forming the product.
Methods using high surface area per volume reactive particulate
A method of processing finely divided reactive particulates (R.sub.Particulate) and forming a product comprising: providing a composite material comprising finely divided reactive particulates (R.sub.Particulate) dispersed in a protective matrix; at least partially exposing the finely divided reactive particulates (R.sub.Particulate); and forming the product.
Methods of producing a titanium alloy product
A method for producing a particulate titanium alloy product can include preparing a composite particulate oxide mixture with TiO.sub.2 powder and at least one alloying element powder. The composite particulate oxide mixture can be co-reduced using a metallic reducing agent under a hydrogen atmosphere at a reduction temperature for a reduction time sufficient to produce a hydrogenated titanium alloy product. The hydrogenated titanium alloy product can then be heat treated under a hydrogen atmosphere and a heat treating temperature to reduce pore size and specific surface area to form a heat treated hydrogenated titanium product. The heat treated hydrogenated titanium product can be deoxygenated to reduce residual oxygen to less than 0.2 wt % to form a deoxygenated hydrogenated titanium product as a particulate. The deoxygenated hydrogenated titanium product can optionally be dehydrogenated to form the titanium alloy product as a particulate.