Method for producing surface-activated superfine nickel powder
A technology of surface activation and production method, applied in the field of metal powder preparation, can solve the problems of difficult implementation, low production efficiency and high cost, and achieve the effects of easy industrialization implementation, reduced consumption cost and low production cost
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Embodiment 1
[0026] Example 1 2 kg of nickel sulfate hexahydrate was prepared into a solution and mixed with excess sodium hydroxide solution, the pH was controlled to be 8-10, and the concentration of ruthenium trichloride was added to 2.5 mg / L, fully stirred, and the slurry was transferred to an autoclave for passage. For hydrogen reaction, control the reaction temperature at 65°C, hydrogen partial pressure at 0.8MPa, react for 40 minutes, take out the liquid-solid separation, wash the solid phase with deionized water three times, and dry it in an oven at 100-120°C. The precursor powder is placed in a belt-type hydrogen reduction furnace with continuous feeding and discharging, and the reduction temperature is controlled at 300°C for 40 minutes to obtain ultra-fine nickel powder with a purity greater than 99.5% and an average particle size of less than 2.0 microns. The ultra-fine nickel powder after being baked can be stored in vacuum packaging.
Embodiment 2
[0027] Example 2 2 kg of nickel sulfate hexahydrate was made into a solution and mixed with excess sodium hydroxide solution, the pH was controlled to be 8-10, and the concentration of ruthenium trichloride was added to be 5 mg / L, fully stirred, and transferred to an autoclave for hydrogen reaction. Control the reaction temperature to 75°C, hydrogen partial pressure to 0.8MPa, react for 40 minutes to take out the liquid-solid separation, wash the solid phase with deionized water three times, and dry it in an oven at 100-120°C. The powder is placed in a belt-type hydrogen reduction furnace with continuous feeding and discharging, and the reduction temperature is controlled at 400°C for 30 minutes to obtain ultra-fine nickel powder with a purity greater than 99.5% and an average particle size of less than 2.0 microns. The ultra-fine nickel powder after being baked can be stored in vacuum packaging.
Embodiment 3
[0028] Example 3 2 kg of nickel sulfate hexahydrate was prepared into a solution and mixed with excess sodium hydroxide solution, the pH was controlled to be 8-10, the concentration of ruthenium trichloride was added to be 10 mg / L, fully stirred, and transferred to an autoclave for hydrogen reaction. Control the reaction temperature to 85°C, hydrogen partial pressure to 0.8MPa, react for 40 minutes to take out the liquid-solid separation, wash the solid phase with deionized water three times, and dry it in an oven at 100-120°C, and dry the precursor The powder is placed in a belt-type hydrogen reduction furnace with continuous feeding and discharging, and the reduction temperature is controlled at 500°C for 30 minutes to obtain ultra-fine nickel powder with a purity greater than 99.5% and an average particle size of less than 2.0 microns. The ultra-fine nickel powder after being baked can be stored in vacuum packaging.
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