Preparation method of composite hydrogen storage material
A technology of hydrogen storage materials and mixed metals, which is applied in the field of preparation of composite hydrogen storage materials, can solve the problems of high hydrogen absorption and desorption temperature, poor cycle stability, etc., achieve high cost performance, avoid long-term high-temperature melting and homogenization treatment effects
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Embodiment 1
[0026] Dissolve 5g of lanthanum nitrate, 2g of nickel chloride, 3g of magnesium nitrate, and 1g of lead nitrate in 200ml of deionized water, add deionized water to make the solution volume 1l, and obtain a mixed metal salt aqueous solution.
[0027] Dissolve 3g of ammonium oxalate, 6g of trisodium nitrilotriacetic acid, 3g of sodium laurylaminopropionate, and 1g of polyvinyl alcohol in 100ml of deionized water. Add 100ml of mixed metal salt aqueous solution dropwise. After dripping, stir for 12 hours and filter with suction. , The solid was dried at 100°C for 4 hours to obtain the hydrogen storage material precursor; 20g hydrogen storage material precursor was crushed into 50nm particles in a ball mill, and then mixed with 10g CaH 2 Mix well, put it in a tube furnace, heat to 500℃ under hydrogen atmosphere, reduce for 3 hours; cool, wash the solid with 100ml deionized water 3 times, 100ml 1M acetic acid aqueous solution 3 times, and then dry at 80℃ After 6 hours, a composite hydro...
Embodiment 2
[0030] Dissolve 10g lanthanum nitrate, 5g nickel chloride, 6g magnesium nitrate, and 3g lead nitrate in 200ml deionized water, add deionized water to make the solution volume 1l, and obtain a mixed metal salt aqueous solution.
[0031] Dissolve 5g ammonium oxalate, 8g trisodium nitrilotriacetic acid, 5g sodium laurylaminopropionate, 3g polyvinyl alcohol in 100ml deionized water, add 100ml mixed metal salt aqueous solution dropwise, after dripping, stir for 24 hours, suction filter , The solid was dried at 100°C for 4 hours to obtain hydrogen storage material precursor; 20g hydrogen storage material precursor was crushed into 100nm particles in a ball mill, and then mixed with 20g CaH 2 Mix uniformly, place in a tube furnace, heat to 650℃ under hydrogen atmosphere, reduce for 6 hours; cool, wash the solid with 100ml deionized water 3 times, 100ml 1M acetic acid aqueous solution 3 times, and then dry at 80℃ After 6 hours, a composite hydrogen storage material was obtained.
[0032] T...
Embodiment 3
[0034] Dissolve 8g of lanthanum nitrate, 4g of nickel chloride, 5g of magnesium nitrate, and 2g of lead nitrate in 200ml of deionized water, add deionized water to the volume of the solution to 1l, and obtain a mixed metal salt aqueous solution.
[0035] Dissolve 4g of ammonium oxalate, 7g of trisodium nitrilotriacetic acid, 4g of sodium laurylaminopropionate, and 2g of polyvinyl alcohol in 100ml of deionized water. Add 100ml of mixed metal salt aqueous solution dropwise. After dripping, stir for 16 hours and filter with suction. , The solid was dried at 100°C for 4 hours to obtain hydrogen storage material precursor; 20g hydrogen storage material precursor was crushed into 80nm particles in a ball mill, and then mixed with 16g CaH 2 Mix uniformly, place in a tube furnace, heat to 600℃ under hydrogen atmosphere, reduce for 4 hours; cool, wash the solid with 100ml deionized water 3 times, 100ml 1M acetic acid aqueous solution 3 times, and then dry at 80℃ After 6 hours, a composite ...
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