Porous iron oxide structured by nanocrystals and preparation method thereof
A technology of nano-iron oxide and iron oxide, which is applied in the direction of iron oxide, iron oxide/iron hydroxide, etc., can solve the problems of soft template method residue and hard template method preparation method, and achieve the effect of simple and controllable method
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Embodiment 1
[0020] Dissolve 1.47g of potassium oxalate in 40.0mL of deionized water and stir to make it evenly dispersed in the solution. The concentration of oxalate is 0.2mol / L; dissolve 3.14g of ammonium ferrous sulfate in 40.0mL of deionized water and stir to make it evenly Dispersed in the solution, the concentration of ferrous ammonium sulfate is 0.2mol / L. Then slowly add the potassium oxalate solution into the ferrous ammonium sulfate solution under constant stirring, the ratio of ferrous ions to oxalate ions is 1:1. After the reaction was completed, it was transferred to a 100 mL hydrothermal kettle, and reacted at 120° C. for 10 hours, and the obtained product was dried at 80° C. for 5 hours to obtain a strip-shaped precursor. figure 1 It is the XRD pattern of the precursor, which is consistent with the standard ferrous oxalate XRD data (JCPDS No. 23-0293), indicating that the crystalline phase of the precursor is ferrous oxalate. The dried precursor ferrous oxalate was placed i...
Embodiment 2
[0022] Dissolve 0.88g potassium oxalate in 40.0mL deionized water, stir to make it evenly dispersed in the solution, the concentration of oxalate is 0.12mol / L; dissolve 1.12g ferrous sulfate in 40.0mL deionized water, stir to make it evenly Dispersed in the solution, the concentration of ferrous sulfate is 0.1mol / L. Then slowly add the potassium oxalate solution into the ferrous sulfate solution under constant stirring, and the ratio of ferrous ions to oxalate ions is 1.2:1. After the reaction was completed, it was transferred to a 100 mL hydrothermal kettle and reacted at 100° C. for 12 hours, and the obtained product was dried at 80° C. for 5 hours to obtain a strip-shaped precursor. The dried precursor ferrous oxalate was placed in a muffle furnace, the temperature was raised to 600°C at a heating rate of 5°C / min and kept for 4 hours, and then slowly cooled to room temperature with the furnace temperature to obtain nanostructured porous iron oxide. The electron microscope ...
Embodiment 3
[0024] Dissolve 0.37g sodium oxalate in 40.0mL deionized water, stir to make it evenly dispersed in the solution, the concentration of oxalate is 0.05mol / L; dissolve 0.800g ammonium ferrous sulfate in 40.0mL deionized water, stir to make it Evenly dispersed in the solution, the concentration of ferrous ammonium sulfate is 0.05mol / L; then slowly add the sodium oxalate solution into the ferrous ammonium sulfate solution under continuous stirring, the content of ferrous ions and oxalate ions The volume ratio is 1:1. After the reaction was completed, it was transferred to a 100 mL hydrothermal kettle, and reacted at 80° C. for 8 hours, and the obtained product was dried at 80° C. for 5 hours to obtain a strip-shaped precursor. The dried precursor ferrous oxalate was placed in a muffle furnace, and the temperature was raised to 600°C at a heating rate of 2°C / min and kept for 4 hours, and then slowly cooled to room temperature with the furnace temperature to obtain nanostructured po...
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