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443 results about "Liquid alloy" patented technology

Liquid Metal Alloys Liquidmetal alloys are a revolutionary class of metal materials that redefine performance, process, and design paradigms.

Vacuum low-pressure casting forming device for titanium alloy component

InactiveCN104028729AImprove feeding capacitySuppresses the tendency to segregate chemical componentsActuatorPressure difference
The invention provides a vacuum low-pressure casting forming device for a titanium alloy component. The vacuum low-pressure casting forming device for the titanium alloy component comprises a device body, a vacuum low-pressure casting pneumatic control system and an electronic control system. An upper chamber and lower chamber type structure is adopted by the device body, a water-cooled copper crucible is arranged in a lower chamber, a casting mold is arranged in an upper chamber, an intermediate separation plate is arranged between the upper chamber and the lower chamber, and a liquid lifting pipe is arranged on the intermediate separation plate. The vacuum low-pressure casting pneumatic control system is connected with the device body, a vacuum system and a protective gas source system, and digital combination valves are adopted as flow regulation actuators. The electronic control system is composed of an industrial control computer and a PLC. After the smelting process of titanium alloy is completed in a smelting chamber, the water-cooled copper crucible is lifted to a casting position through a lifting device, an upper chamber and lower chamber intercommunication valve is closed, the flow of protective gas fed into the lower chamber is controlled through the computer, the pressure difference between the upper chamber and the lower chamber is established, the liquid alloy is filled in the casting mold through the liquid lifting pipe under the action of the pressure difference, and the casting process is completed. Compared with traditional centrifugal casting and bottom leakage type suction casting, the mold-filling capacity and solidification feeding capacity of the titanium alloy can be improved, castings with better casting quality and thinner wall thicknesses can be obtained, and a new means is provided for batch production of minitype titanium alloy components.
Owner:NORTHWESTERN POLYTECHNICAL UNIV

Silica gel compositions containing alkali metals and alkali metal alloy

The invention relates to Group 1 metal/silica gel compositions comprising silica gel and an alkali metal or an alkali metal alloy. The compositions of the inventions are described as Stage 0, I, II, and III materials. These materials differ in their preparation and chemical reactivity. Each successive stage may be prepared directly using the methods described below or from an earlier stage material. Stage 0 materials may, for example, be prepared using liquid alloys of Na and K which are rapidly absorbed by silica gel (porous SiO2) under isothermal conditions, preferably at or just above room temperature, to form loose black powders that retain much of the reducing ability of the parent metals. When the low melting Group 1 metals are absorbed into the silica gel, a mild exothermic reaction produces Stage I material, loose black powders that are indefinitely stable in dry air. Subsequent heating to 400° C. produces Stage II materials, which are also loose black powders. Further heating above 400° C. forms Stage III material with release of some Group 1 metal. It is believed that Stage I, II and III materials represent reductions of the silica gel after absorption of the Group 1 metal. Preferred Group 1 metal/silica gel compositions of the invention are those containing sodium, potassium, or sodium-potassium alloys with sodium and sodium-potassium alloys being most preferred. Each stage of the Group 1 metal/silica gel composition of the invention may be used as a reducing agent reacting with a number of reducible organic materials in the same manner known for alkali metals and their alloys.
Owner:SIGNA CHEM INC +1

Silica gel compositions containing alkali metals and alkali metal alloys

The invention relates to Group 1 metal / silica gel compositions comprising silica gel and an alkali metal or an alkali metal alloy. The compositions of the inventions are described as Stage 0, I, II, and III materials. These materials differ in their preparation and chemical reactivity. Each successive stage may be prepared directly using the methods described below or from an earlier stage material. Stage 0 materials may, for example, be prepared using liquid alloys of Na and K which are rapidly absorbed by silica gel (porous SiO2) under isothermal conditions, preferably at or just above room temperature, to form loose black powders that retain much of the reducing ability of the parent metals. When the low melting Group 1 metals are absorbed into the silica gel, a mild exothermic reaction produces Stage I material, loose black powders that are indefinitely stable in dry air. Subsequent heating to 400° C. produces Stage II materials, which are also loose black powders. Further heating above 400° C. forms Stage III material with release of some Group 1 metal. It is believed that Stage I, II and III materials represent reductions of the silica gel after absorption of the Group 1 metal. Preferred Group 1 metal / silica gel compositions of the invention are those containing sodium, potassium, or sodium-potassium alloys with sodium and sodium-potassium alloys being most preferred. Each stage of the Group 1 metal / silica gel composition of the invention may be used as a reducing agent reacting with a number of reducible organic materials in the same manner known for alkali metals and their alloys.
Owner:SIGNA CHEM INC +1

High-strength antibacterial aluminum alloy for aluminum alloy ladder and preparation method thereof

The invention relates to the technical field of aluminum alloy ladder preparation, and particularly relates to high-strength antibacterial aluminum alloy for an aluminum alloy ladder and a preparation method thereof. The aluminum alloy comprises a high-strength aluminum alloy matrix and a micro-arc oxidation film, wherein the micro-arc oxidation film is arranged on the surface of the aluminum alloy matrix, the weight of a hole sealing agent on the micro-arc oxidation film is 0.15 g / cm<2> to 0.90 g / cm<2>, and the hole sealing agent covers at least 92% of micropores in the micro-arc oxidation film. The preparation method comprises the steps of smelting metal, modifying, refining and degassing, pouring and forming and performing quenching treatment, aging treatment, micro-arc oxidation and hole sealing treatment, wherein in the step of modifying, nanometer modificators are uniformly dispersed into liquid alloy obtained by smelting; in the step of refining and degassing, 0.23% to 0.38% of hexachloroethane is added to the modified liquid alloy so as to refine and degas; and the aging treatment is divided into four-stage aging treatment. The aluminum alloy prepared by adopting the preparation method has the characteristics of high hardness, high strength, wear resistance, corrosion resistance, good anti-cracking performance, good antibacterial effect, difficulty in aging and deformation and long service life.
Owner:浙江洋铭实业有限公司

High strength nickel base corrosion resistance alloy and manufacturing method thereof

ActiveCN102899582AConducive to refining the initial solidification structure of continuous castingImprove mechanical propertiesTurbineMechanical property
The present invention relates to a high strength nickel base corrosion resistance alloy, which has the following components, by mass, 0.06-0.10% of C, less than or equal to 1.0% of Si, less than or equal to 1.50% of Mn, 19.0-23.0% of Cr, less than or equal to 0.035% of P, less than or equal to 0.001% of S, less than or equal to 0.020% of N, 29.0-35.0% of Ni, 0.15-0.6% of Ti, 0.15-0.6% of Al, 0.001-0.005% of Mg, less than or equal to 0.5% of Cu+O, and the balance of Fe and unavoidable impurities. The nickel base corrosion resistance alloy has a fully austenite structure, and forms MgO and/or MgO.Al2O3 particles with a diameter of about 10 nm-1 mum and a number of 30-50/mm<2> in a liquid alloy so as to refine the diameter of the initial solidified grains of the alloy continuous casting billet to about 0.5-1.0 mm. In addition, a vertical continuous casting process is adopted to produce, such that surface cracks of the continuous casting billet are avoided; and the grain size of the final product is controlled to the 3.5-4 level, such that the product has characteristics of excellent mechanical property, excellent high temperature creep resistance, and the like, and is suitable for manufacture of parts of furnace devices, heat exchangers, steam-powered turbines, and the like.
Owner:BAOSHAN IRON & STEEL CO LTD

Pressure difference injection moulding method and equipment for amorphous magnesium alloy

The invention provides an amorphous magnesium alloy differential pressure injection molding method and equipment thereof and pertains to the technical field of alloy preparation engineering and equipment. A mould (10) is cooled; a mother alloy is added in from the upper end of a compression chamber (7); an upper compression bar (3) goes down to the place over the compression chamber (7); a working cavity (12) is vacuumized by a vacuum pump (16); the compression chamber (7) is heated by a heater coil (6) so as to cause the mother alloy to be melted; a quick-opening valve (19) is opened, the upper compression bar (3) and a lower compression bar (4) go down for carrying out the injection, and the liquid alloy is injected into a die cavity of a mould (10); the liquid ally is solidified and the amorphous magnesium alloy is obtained; the operation of injection is finished. The equipment includes the upper compression bar (3), the lower compression bar (4), the heater coil (6) and a working chamber (12), etc. The method and the equipment of the invention have high heating efficiency; the molten bath of magnesium alloy can be cooled quickly; the operation of differential pressure injection is simple, the applicability is better, the working is stable and reliable, and the process is easy to be controlled, thus being very suitable for preparing bulk amorphous magnesium alloy.
Owner:TSINGHUA UNIV

Method for preparing molybdenum nickel alloy by directly reducing and smelting molybdenum nickel ore

The invention relates to a method for preparing molybdenum nickel alloy by directly reducing and smelting molybdenum nickel ore. The method comprises the following steps: grinding the molybdenum nickel ore into molybdenum nickel ore powder with the average particle size of less than or equal to 0.18 mm; adding a slag forming agent and a reducing agent with the average particle size of less than or equal to 0.18 mm into the molybdenum nickel ore powder to obtain furnace charge; mixing the furnace charge uniformly and pelletizing to obtain pellet; heating the pellet to 1,600 to 1,800 DEG C; smelting; and collecting liquid alloy, slag, smoke dust and furnace gas respectively, wherein the liquid alloy is crude molybdenum nickel alloy; the direct yield of the molybdenum and the nickel is 96 percent and 94 percent respectively; the molybdenum content of the smoke dust is less than 0.2 percent and the nickel content of the smoke dust is less than 0.2 percent; and the SO2 concentration of thefurnace gas is less than or equal to 400 mg / m<3>. The process method is simple and reasonable, and convenient to operate; the molybdenum nickel ore is not subjected to oxidizing roasting de-sulfuration; and the crude molybdenum nickel alloy is prepared by directly reducing and smelting the molybdenum nickel ore and by using the carbon of the molybdenum nickel ore as a reducing agent, so that indirect smelting is changed into direct smelting. The prepared molybdenum nickel alloy is low in sulfur content and phosphorus content, environment friendly and low in production cost; and the method is suitable for extraction of the molybdenum nickel ore.
Owner:CENT SOUTH UNIV +2

Silicide compositions containing alkali metals and methods of making the same

The invention relates to Group 1 metal/silica gel compositions comprising silica gel and an alkali metal or an alkali metal alloy. The compositions of the inventions are described as Stage 0, I, II, and III materials. These materials differ in their preparation and chemical reactivity. Each successive stage may be prepared directly using the methods described below or from an earlier stage material. Stage 0 materials may, for example, be prepared using liquid alloys of Na and K which are rapidly absorbed by silica gel (porous Si02) under isothermal conditions, preferably at or just above room temperature, to form loose black powders that retain much of the reducing ability of the parent metals. When the low melting Group 1 metals are absorbed into the silica gel, a mild exothermic reaction produces Stage I material, loose black powders that are indefinitely stable in dry air. Subsequent heating to 400 DEG C produces Stage II materials, which are also loose black powders. Further heating above 400 DEG C forms Stage III material with release of some Group 1 metal. It is believed that Stage I, II and III materials represent reductions of the silica gel after absorption of the Group 1 metal. Preferred Group 1 metal/silica gel compositions of the invention are those containing sodium, potassium, or sodium-potassium alloys with sodium and sodium- potassium alloys being most preferred. Each stage of the Group 1 metal/silica gel composition of the invention may be used as a reducing agent reacting with a number of reducible organic materials in the same manner known for alkali metals and their alloys.
Owner:SIGNA CHEM INC +1

Gallium liquid metal material and application of gallium liquid metal material to teletransmission pressure and different pressure transmitter

The invention discloses application of a gallium liquid metal material to a teletransmission pressure and different pressure transmitter. The pressure and different pressure transmitter is provided with a capillary tube filled with a liquid medium, and the whole or part of the capillary tube is filled with the gallium liquid metal material. According to parameter requirements of the gallium liquid metal material, the heat conductivity is larger than 10 W/m*k, the kinematic viscosity is (5*10-8-9*10-8) m<2>/s, the melting point is lower than 15 DEG C, and the boiling point is larger than 1000 DEG C. The gallium liquid metal material is gallium liquid metal or gallium-based liquid alloy metal. The application has the beneficial effects that the gallium liquid metal material with the very high nominal melting point is used on the pressure and different pressure transmitter, the gallium liquid metal material is not liable to be vaporized even the nominal high-temperature boundary point is approached, the gallium liquid metal material still has very good fluidity, the performance cannot be affected, and sensitivity and precision of a measuring instrument are maintained. The highest use temperature of the gallium liquid metal material can be 1200 DEG C or higher, and the gallium liquid metal material can also be used on high-temperature and negative-pressure occasions.
Owner:SHANGHAI ROCKSENSOR AUTOMATION
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