Method of preparing Mn3O4 porous materials
A porous material, 5min technology, applied in manganese oxide/manganese hydroxide and other directions, can solve the problems of porous structure collapse cost, porous materials are not widely reported, etc., to achieve low cost, easy large-scale synthesis, good crystallinity effect
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Embodiment 1
[0016] 1) Dissolve 1.1 g manganese acetate dihydrate in 30 ml ethanol, then add 0.8 ml formic acid, stir until uniform to obtain a suspension.
[0017] 2) Transfer the suspension to a solvothermal device, perform a solvothermal reaction at 150 °C for 6 h, then centrifuge the obtained material, and then dry it at 80 °C.
[0018] 3) Heat the dried powder at 200°C for 12 h to obtain Mn 3 o 4 porous material.
[0019] Prepared Mn 3 o 4 The X-ray diffraction pattern of the porous material is shown in Figure 1, and its diffraction peaks are similar to those of hausmannite Mn 3 o 4 The standard spectrum is consistent, indicating that the obtained product is black manganese ore Mn 3 o 4 . Calculated by Scherrer's formula, the average crystal diameter is 20 nm. Figure 2 shows the Mn prepared in this example 3 o 4 Scanning electron micrographs of porous materials. It can be seen from the figure that Mn 3 o 4 Porous materials have a large number of mesoporous and macropo...
Embodiment 2
[0021] 1) Dissolve 1.1 g manganese acetate dihydrate in 30 ml ethanol, then add 0.8 ml formic acid, stir until uniform to obtain a suspension.
[0022] 2) The suspension was centrifuged, and the resulting substance was dried at 80°C.
[0023] 3) Heat the dried powder at 200°C for 12 h to obtain Mn 3 o 4 porous material.
[0024] Prepared Mn 3 o 4 SEM images of porous materials such as Figure 4 shown. It can be seen from the figure that the prepared Mn 3 o 4 The porous material is ellipsoidal, and a large number of pore structures are distributed on the sphere.
Embodiment 3
[0026] 1) Dissolve 1.1 g of manganese acetate dihydrate in 30 ml of methanol, then add 1 ml of formic acid, stir until uniform to obtain a suspension.
[0027] 2) Transfer the suspension to a solvothermal device, perform a solvothermal reaction at 170 °C for 12 h, then centrifuge the obtained material, and then dry it at 80 °C.
[0028] 3) Heat the dried powder at 400°C for 3 h to obtain Mn 3 o 4 porous material.
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