Magnetic ferrocobalt ferrite prepared by hard formwork method and preparation method thereof
A hard template method and ferrite technology are applied in the field of new cobalt ferrite and its preparation, and achieve the effects of low equipment requirements, simple process and good UV light degradation performance
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Embodiment 1
[0035] A. 3.9 grams of Co (NO 3 ) 2 ·6H 2 O, 4.6 g FeSO 4 ·7H 2 O and 2.6 g Fe 2 (SO 4 ) 3 Place in 50.0 ml of 1.0% high quality wood pulp and stir until the solid mixture is fully dissolved.
[0036] B. Prepare 1.5M NaOH and 1.0M Na with deoxygenated deionized water 2 CO 3 50.0 ml of mixed alkali solution, and under nitrogen protection and vigorous stirring, slowly add the alkali solution dropwise to the above salt solution until pH ≈ 10.5, then continue to stir for 6.0 hours, stand for 16.0 hours at room temperature for crystallization, filter , and washed three times with deionized water and absolute ethanol, respectively. The solid substance is vacuum dried to obtain a cobalt iron iron hydrotalcite / paper fiber adsorption assembly.
[0037] C. The adsorption assembly is placed in a muffle furnace, and the muffle furnace is heated to 1100 °C at a heating rate of 5.0 °C / min, and kept for 2 hours to obtain a cobalt ferrite microtube.
Embodiment 2
[0041] A. Weigh 4.1 grams of Co (NO 3 ) 2 ·6H 2 O, 3.9 g FeSO 4 ·7H 2 O and 2.8 g Fe 2 (SO 4 ) 3 Place in 50.0 ml of 1.0% high quality wood pulp and stir until the solid mixture is fully dissolved. Separately prepare 2.5M NaOH and 1.8M Na with deoxygenated deionized water 2 CO 3 50.0 ml of mixed alkali solution of 50.0 ml, under nitrogen protection and vigorous stirring, slowly drop the mixed alkali solution into the above three-necked flask containing the salt solution until pH ≈ 10.5, and then continue to stir for 6.0 hours.
[0042] B. After stirring, the product was left to stand for crystallization for 16.0 hours at room temperature.
[0043] C. Filter the above mixture and wash with deionized water and absolute ethanol for 3 times successively.
[0044] D, vacuum drying solid matter, obtain Co 2+ Fe 2+ Fe 3+ -LDH / paper fiber adsorption assembly.
[0045] E. Place the adsorption assembly in a muffle furnace, heat the muffle furnace to 1100 °C at a heating ra...
Embodiment 3
[0048] A. Weigh 5.8 grams of Co (NO 3 ) 2 ·6H 2 O, 5.6 g FeSO 4 ·7H 2 O and 8.1 g Fe 2 (SO 4 ) 3 Place in 50.0 ml of 1.0% high quality wood pulp and stir until the solid mixture is fully dissolved. Separately prepare 2.5M NaOH and 2.0M Na with deoxygenated deionized water 2 CO 3 50.0 ml of mixed alkali solution of 50.0 ml, under nitrogen protection and vigorous stirring, slowly drop the mixed alkali solution into the above three-necked flask containing the salt solution until pH ≈ 10.5, and then continue to stir for 6.0 hours.
[0049] B. After stirring, the product was left to stand for crystallization for 16.0 hours at room temperature.
[0050] C. Filter the above mixture and wash with deionized water and absolute ethanol for 3 times successively.
[0051] D, vacuum drying solid matter, namely get Co 2+ Fe 2+ Fe 3+ -LDH / paper fiber adsorption assembly.
[0052] E. Place the adsorption assembly in the muffle furnace at 5.0. The muffle furnace was heated to 110...
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