Preparation method of active nano-aluminium oxide for coating
A nano-alumina and active technology, applied in the field of fine chemicals, can solve the problems of affecting the performance of powder coatings, it is difficult to prevent particles from coarsening hard agglomerates, and the cost is high, so as to improve thermal stability and specific surface area, eliminate hard Agglomeration phenomenon, the effect of mild production conditions
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[0024] The preparation process of the present invention is as follows:
[0025]
[0026] The basic steps are: firstly, take aluminum ammonium sulfate and ammonium carbonate and dissolve them in secondary water respectively to make a stock solution; secondly, take the above stock solution and add polyethylene glycol to prepare polyethylene glycol-aluminum ammonium sulfate The mixed solution of the mixed solution of polyethylene glycol-ammonium carbonate; the third is after adjusting the pH value, adding the mixed solution of polyethylene glycol-ammonium aluminum sulfate in the mixed solution of polyethylene glycol-ammonium carbonate, stirring, Centrifugation, washing, and drying; the fourth is azeotropic distillation and dehydration; the fifth is high-temperature calcination.
[0027] The step of preparing a kind of active nano-alumina powder for coating is as follows:
[0028] 1. Weigh ammonium aluminum sulfate and ammonium carbonate, dissolve them in double distilled wate...
Embodiment 1
[0038] Embodiment 1: under the magnetic stirring of 1300r / min, the concentration that will contain 10wt% PEG2000 is the NH of 0.44mol / L 4 Al(SO 4 ) 2 The solution is added with the concentration of 0.80mol / L (NH 4 ) 2 CO 3 In the solution (pH 9.3), after the titration is completed, continue to stir for 0.5 h; centrifuge, wash 4 times with secondary water and 3 times with ethanol, dry at 80°C for 4 h, remove surface water, and obtain a dry powder. Add the obtained dry powder into 80ml of n-butanol, after ultrasonic dispersion, reflux for 2h, distill and remove the n-butanol-water azeotrope at 93°C, when the fraction temperature rises to the boiling point of n-butanol at 117°C, After stopping the distillation and continuing to reflux for 2 h, the n-butanol was recovered by distillation under reduced pressure to obtain a loose powder.
[0039] Calcined at 900°C to obtain γ-Al 2 o 3 product, its particle morphology see figure 1 , good particle size and shape uniformity, go...
Embodiment 2
[0040] Embodiment 2: Under the magnetic stirring of 1300r / min, the NH containing 2wt% PEG2000 concentration is 0.44mol / L 4 Al(SO 4 ) 2 The solution is added into an equal volume of (NH 4 ) 2 CO 3 In the solution (pH 9.3), after the titration is completed, continue to stir for 0.5 h; centrifuge, wash 4 times with secondary water and 3 times with ethanol, dry at 80°C for 4 h, remove surface water, and obtain a dry powder. Add the obtained dry powder into 80ml of n-butanol, after ultrasonic dispersion, reflux for 2h, distill and remove the n-butanol-water azeotrope at 93°C, when the fraction temperature rises to the boiling point of n-butanol at 117°C, After stopping the distillation and continuing to reflux for 2 h, the n-butanol was recovered by distillation under reduced pressure to obtain a loose powder.
[0041] Calcined at 900°C to obtain γ-Al 2 o 3 product, its particle morphology see image 3 , the uniformity of particle size and shape is good, there is some hard ...
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