A preparation method of ordered mesoporous iron oxyhydroxide nanorods
An iron oxide nanometer, mesoporous hydroxyl technology, applied in the direction of iron oxide/iron hydroxide, etc., can solve the problems of complex crystal phase, skeleton collapse, affecting the order degree of mesopores, etc. Inexpensive and readily available effects
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Embodiment 1
[0035] (1) Dissolve 0.5g of non-ionic block copolymer surfactant in 35mL of distilled water, add anhydrous ferric chloride, stir and disperse fully to obtain a yellow solution.
[0036] (2) While stirring the yellow solution, 0.5 g of urea precipitation agent was added dropwise at a rate of 1.5 mL / min, and stirred at a constant temperature of 30 ° C for 12 h to obtain a precursor solution.
[0037] (3) Transfer the precursor solution to a reaction kettle with a polytetrafluoroethylene liner, conduct a hydrothermal reaction at 80°C, and centrifuge to collect the precipitate. After the precipitate is fully washed with ethanol and water, it is vacuum-dried overnight at 100°C. , to obtain solid powder.
[0038] (4) Transfer the solid powder to a crucible, and in an inert atmosphere, start from room temperature at a rate of 5 °C / min to 150 °C, keep the temperature for 2.5 h, and cool down naturally to obtain ordered mesoporous iron oxyhydroxide nanorods.
Embodiment 2
[0040](1) Dissolve 2 g of the nonionic block copolymer surfactant PEOPPOPEO in 80 mL of distilled water, add ferric nitrate, stir and disperse fully to obtain a yellow solution.
[0041] (2) While stirring the yellow solution, 2 g of urea precipitation agent was added dropwise at a rate of 3 mL / min, and stirred at a constant temperature of 60 °C for 48 h to obtain a precursor solution.
[0042] (3) Transfer the precursor solution to a reaction kettle with a polytetrafluoroethylene liner, react hydrothermally at 120°C, centrifuge to collect the precipitate, wash the precipitate fully with ethanol and / or water, and vacuum at 100°C Dry overnight to obtain a solid powder.
[0043] (4) Transfer the solid powder into a crucible, and in an inert atmosphere, start from room temperature at a rate of 5 °C / min to 250 °C, keep it warm for 2.5 h, and cool down naturally to obtain ordered mesoporous iron oxyhydroxide nanorods.
Embodiment 3
[0045] (1) Dissolve 1 g of non-ionic block copolymer surfactant in 45 mL of distilled water, add hydrous ferric chloride, stir and disperse fully to obtain a yellow solution.
[0046] (2) While stirring the yellow solution, 1.5 g of urea precipitation agent was added dropwise at a rate of 2 mL / min, and stirred at a constant temperature of 40 °C for 24 h to obtain a precursor solution.
[0047] (3) Transfer the precursor solution to a reaction kettle with a polytetrafluoroethylene liner, conduct a hydrothermal reaction at 120°C, centrifuge to collect the precipitate, wash the precipitate with ethanol or water, and dry it under vacuum at 100°C overnight , to obtain solid powder.
[0048] (4) Transfer the solid powder to a crucible, and in an inert atmosphere, start from room temperature at a rate of 5 °C / min to 200 °C, keep it warm for 2.5 h, and cool down naturally to obtain ordered mesoporous iron oxyhydroxide nanorods.
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Abstract
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Application Information
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