Preparation method of composite oxide
A composite oxide and solution technology, applied in chemical instruments and methods, catalyst activation/preparation, chemical/physical processes, etc., can solve the problems of inhibiting large-scale application, difficult industrial application, poor material performance, etc., and achieve low stacking The effect of density, low cost and high catalytic performance
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Embodiment 1
[0021] 7.7g Mg(NO 3 ) 2 ·6H 2 O, 22.5g Al(NO 3 ) 3 9H 2 O dissolved in 35ml H 2 O forms A liquid; 12g (NH 4 ) 2 CO 3 dissolved in 41ml H 2 O, forming liquid B. Liquids A and B were cooled to -28°C, then quickly mixed, stirred and ground, and the reaction liquid solidified rapidly to obtain a powdery substance. Place it at -28°C for 12 hours, then thaw the formed powder, add water to dissolve impurities, filter, dry at 110°C, and bake at 700°C for 2 hours to obtain MgAl with a perfect spinel crystal phase 2 o 4 powder. The bulk density of the material is 0.138g / ml, and the specific surface area is 326.5m 2 / g. Compared with other methods, (NH 4 ) 2 CO 3 The sample obtained by co-precipitation method is 66m 2 / g [Br.Ceram.Trans.J.91 volume, 77 pages], the sample obtained by dialkoxide hydrolysis method is 160m 2 / g [Chem. Mater. Vol. 8, p. 2850].
Embodiment 2
[0023] 4.3g La(NO 3 ) 3 ·6H 2 O, 2.3ml 50wt.% Mn(NO 3 ) 3 The solution was dissolved in 6ml H 2 O forms liquid A; 2.1g Na 2 CO 3 , 0.8g NaOH dissolved in 8ml H 2 O, forming liquid B. Liquids A and B were cooled to -23°C, then quickly mixed, stirred and ground, and the reaction liquid solidified rapidly to obtain a powdery substance. Place it in an environment of -23°C for 12h, then thaw the formed powder, add water to dissolve impurities, filter, dry at 110°C, and bake at 700°C for 2h to obtain LaMnO with a perfect perovskite crystal phase 3 powder. The specific surface of the material is 42.7m 2 / g.
Embodiment 3
[0025] 3.3g Ce(NO 3 ) 3 ·6H 2 O, 1.8g ZrOCl 2 dissolved in 7ml H 2 O forms liquid A; 6ml of 10mol / L ammonia water becomes liquid B. Liquids A and B were cooled to -34°C, then quickly mixed, stirred and ground, and the reaction liquid solidified rapidly to obtain a powdery substance. Place it in an environment of -34°C for 12h, then thaw the formed powder, add water to dissolve impurities, filter, dry at 110°C, and bake at 800°C for 2h to obtain Ce with a perfect crystal phase. 0.75 Zr 0.25 o 2 Solid solution, the specific surface is 97.5m 2 / g.
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