Preparation method of cerium lanthanium complex oxide
A composite oxide, cerium lanthanum technology, applied in chemical instruments and methods, rare earth metal compounds, chemical/physical processes, etc., can solve the problem of difficult to obtain microscopic uniformity, unsatisfactory effect of catalytic elimination of VOCs, and difficult control of preparation process conditions, etc. question
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[0020] Refer to the above preparation steps
[0021] Weigh Ce(NO 3 ) 3 ·6H 2 O, La(NO 3 ) 4 ·6H 2 O, add appropriate amount of water to dissolve and set aside. The molar ratio of the above substances is: X:1-X (X=0.1-0.9).
[0022] Slowly add the above-mentioned mixed solution dropwise in an aqueous solution containing polyethylene glycol (molecular weight is 6000-20000) weight percent of 1-10wt%, under magnetic stirring conditions, when the pH value of the solution is adjusted to 9-10 with ammonia water, Dropping was stopped.
[0023] After continuing to stir the above solution for 10-20 minutes, keep the solution at -5-0° C. for 20-30 hours.
[0024] Remove the solvent by suction filtration of the solution, dissolve the gel in n-butanol which is 8-10 times of the weight of the gel in n-butanol, heat in a three-necked flask, and when it reaches 93-100°C, the azeotrope is evaporated After the water is completely removed, the temperature rises rapidly to 118°C, the boi...
Embodiment 2
[0027] A specific embodiment of the preparation of cerium-lanthanum composite oxide powder, the steps are:
[0028] (1) Calculate and weigh 5.05-15.5g Ce (NO 3 ) 3 ·6H 2 O, 9.00-0.5g La(NO 3 ) 4 ·6H 2 O, add appropriate amount of water to dissolve and set aside.
[0029] (2) Slowly add the mixed solution described in ① in 100ml of aqueous solution containing polyethylene glycol (molecular weight: 20000) 5g, under magnetic stirring conditions, when the pH value of the solution is adjusted to 9-10 with ammonia water, stop the dripping .
[0030] (3) After continuing to stir for 15 minutes, the solution was kept at -5°C for 24 hours.
[0031] (4) Then the solution is suction filtered to remove the solvent, and the solid is dissolved in excess n-butanol, and heated in a three-necked flask. When it reaches 93-100°C, the azeotrope is distilled off, and the water is completely removed. Afterwards, the temperature rose rapidly to the boiling point of n-butanol, 118°C, and cont...
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