Preparation method of multi-component hydrogen storage composite material
A composite material and hydrogen storage technology, applied in the field of preparation of multi-component hydrogen storage composite materials, can solve the problems of high hydrogen absorption and desorption temperature, poor cycle stability, etc., and achieve the effects of high cost performance, avoiding long-term high-temperature melting and homogenization treatment
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Embodiment 1
[0027] Dissolve 3 g of indium chloride, 4 g of stannous chloride, 3 g of calcium nitrate, and 4 g of bismuth nitrate in 200 ml of deionized water, and add deionized water until the volume of the solution is 1 l to obtain an aqueous solution of mixed metal salts.
[0028] Dissolve 1g of urea, 4g of diammonium hydrogen phosphate, 1g of sodium hexadecylsulfonate, and 2g of sodium polyacrylate in 100ml of deionized water, add dropwise 100ml of a mixed metal salt solution, and stir for 12 hours after dropping, and filter with suction. Dry at 120°C for 3 hours to obtain the precursor of the hydrogen storage material; crush 15g of the precursor of the hydrogen storage material into 50nm particles in a ball mill, mix it with 20g of LiAlH4 evenly, place it in a tube furnace, and heat it to 600 ℃, reduced for 2 hours, cooled, and the solid was washed three times with 100ml deionized water and 3 times with 100ml 1M acetic acid aqueous solution, and then dried at 100℃ for 4 hours to obtain...
Embodiment 2
[0031] Dissolve 5 g of indium chloride, 6 g of stannous chloride, 5 g of calcium nitrate, and 6 g of bismuth nitrate in 200 ml of deionized water, and add deionized water until the volume of the solution is 1 l to obtain an aqueous solution of mixed metal salts.
[0032] Dissolve 3g of urea, 6g of diammonium hydrogen phosphate, 3g of sodium hexadecylsulfonate, and 4g of sodium polyacrylate in 100ml of deionized water, add dropwise 100ml of a mixed metal salt solution, and stir for 24 hours after dropping, and filter with suction. Dry at 120°C for 3 hours to obtain the precursor of the hydrogen storage material; crush 15 g of the precursor of the hydrogen storage material into 100 nm particles in a ball mill, and then mix it with 30 g of LiAlH 4 Mix evenly, place in a tube furnace, heat to 750°C under a hydrogen atmosphere, reduce for 3 hours, cool, wash the solid with 100ml deionized water three times, 100ml 1M acetic acid aqueous solution for three times, and then dry at 100°C...
Embodiment 3
[0035] Dissolve 3.5 g of indium chloride, 4.5 g of stannous chloride, 3.5 g of calcium nitrate, and 4.5 g of bismuth nitrate in 200 ml of deionized water, and add deionized water until the volume of the solution is 1 l to obtain a mixed metal salt solution.
[0036] Dissolve 1.5g of urea, 4.5g of diammonium hydrogen phosphate, 1.5g of sodium hexadecylsulfonate, and 2.5g of sodium polyacrylate in 100ml of deionized water, add 100ml of mixed metal salt aqueous solution dropwise, stir for 12 hours, and pump Filter, and dry the solid at 120°C for 3 hours to obtain a hydrogen storage material precursor; crush 15g of the hydrogen storage material precursor into 80nm particles in a ball mill, then mix it with 25gLiAlH4 evenly, place it in a tube furnace, and under a hydrogen atmosphere Heating to 600°C, reducing for 2 hours, cooling, washing the solid with 100ml of deionized water three times, 100ml of 1M acetic acid aqueous solution for three times, and drying at 100°C for 4 hours to...
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