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Method for mfg. lanthana nanopowder

A technology of nano-lanthanum oxide and powder, applied in the field of chemical industry, can solve problems such as difficult to effectively control the particle size of rare earth oxide precursors, unable to limit the degree of precipitation reaction, wide particle size distribution, etc.

Inactive Publication Date: 2003-03-12
XI AN JIAOTONG UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

Due to the large concentration gradient of the reactants in the common precipitation method, the particle size distribution of the rare earth oxide precursor is wide; the traditional uniform precipitation method cannot limit the extent of the precipitation reaction, and it is difficult to effectively control the particle size of the rare earth oxide precursor
Therefore, the above preparation process is difficult to control the particle size and particle size distribution of the final synthesized nanopowder

Method used

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Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0024] Embodiment 1: According to the technical scheme of the present invention, 20.5gCTAB and 10ml n-hexanol were added in 120ml cyclohexane under magnetic stirring respectively. Then add 10 ml of mixed solution of lanthanum nitrate and dimethyl oxalate, wherein the concentration of lanthanum nitrate is 0.12 mol / l, and the concentration of dimethyl oxalate is 0.18 mol / l. Stir at room temperature until a clear microemulsion is obtained. The concentration of the surfactant in the microemulsion is 0.4 mol / l, the concentration of the co-surfactant is 0.55 mol / l, and the volume ratio of the organic solvent to A is 12:1. The microemulsion was heated to 85°C and stirred at 85°C for 15h. Then under the reduced pressure of the water pump, cyclohexane is recovered by distillation. The residue was washed three times each with deionized water and 95% ethanol. The obtained precipitate was vacuum-dried at 45°C for 3 hours, and then calcined at 650°C for 1 hour to obtain nanometer lantha...

Embodiment 2

[0025] Embodiment 2: According to the technical scheme of the present invention, 15gCTAB and 12ml n-heptanol were added in 120ml cyclohexane under magnetic stirring respectively. Then add 15 ml of mixed solution of lanthanum nitrate and dimethyl oxalate, wherein the concentration of lanthanum nitrate is 0.18 mol / l, and the concentration of dimethyl oxalate is 0.18 mol / l. Stir at room temperature until a clear microemulsion is obtained. The concentration of the surfactant in the microemulsion is 0.26 mol / l, the concentration of the co-surfactant is 0.56 mol / l, and the volume ratio of the organic solvent to A is 8:1. The microemulsion was heated to 40°C and stirred at 40°C for 18h. Then under the reduced pressure of the water pump, cyclohexane is recovered by distillation. The residue was washed three times each with deionized water and 95% ethanol. The obtained precipitate was vacuum-dried at 45°C for 3 hours, and then calcined at 800°C for 1 hour to obtain nanometer lanthan...

Embodiment 3

[0026] Embodiment 3: According to the technical scheme of the present invention, 12.1g NP-9 and 20ml n-hexanol were added into 200ml cyclohexane under magnetic stirring respectively. Then add 23 ml of mixed solution of lanthanum nitrate and dimethyl oxalate, wherein the concentration of lanthanum nitrate is 0.12 mol / l, and the concentration of dimethyl oxalate is 0.18 mol / l. Stir at room temperature until a clear microemulsion is obtained. The concentration of the surfactant in the microemulsion is 0.08 mol / l, the concentration of the co-surfactant is 0.66 mol / l, and the volume ratio of the organic solvent to A is 8.7:1. The microemulsion was heated to 50°C and stirred at 50°C for 12h. Then under the reduced pressure of the water pump, cyclohexane is recovered by distillation. The residue was washed three times each with deionized water and 95% ethanol. The obtained precipitate was vacuum-dried at 60°C for 3 hours, and then calcined at 750°C for 2 hours to obtain nanometer ...

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Abstract

A process for preparing lanthanum oxide nanoparticles includes preparing water-in-oil microemulsion from the solution of surfactant, co-surfactant, non-polar organic solvent, dimethyl oxalate and lanthanum nitrate, heating, reaction, vacuum evaporation of solvent, washing precipitate with alcohol and water, drying and calcining.

Description

[0001] 1. Field [0002] The invention belongs to the field of chemical industry and relates to a method for preparing oxides, in particular to a chemical method for preparing nanometer lanthanum oxide powder. 2. Background technology [0003] In recent years, the specific properties of lanthanum oxide nanopowders in the fields of superconductivity, magnetism, catalysis, optics and functional devices have attracted great attention. The synthesis of nanopowders has become an important research field in chemistry and materials science, and the preparation of nanopowders with a certain particle size and narrow particle size distribution is particularly critical. A variety of nanopowder preparation methods have been reported at home and abroad, which can be divided into physical methods and chemical methods. The physical methods mainly include evaporation condensation method, mechanical alloy method and pulverization method. Chemical laws mainly include vapor deposition method, ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01B13/14C01G17/00
Inventor 杨伯伦贺拥军
Owner XI AN JIAOTONG UNIV
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