Preparation method for nano-copper with oxidation resistance and dispersibility
A technology of anti-oxidation and dispersibility, applied in the field of nanomaterials, to achieve the effect of good monodispersity, uniform particle size, easy transportation and storage
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Embodiment 1
[0024] (1) Disperse 3.70 g of copper glycinate and 0.02 g of dispersant sodium dodecylbenzenesulfonate in 300 mL of distilled water, and obtain a mixed solution by magnetic stirring and ultrasonic dispersion;
[0025] (2) Heat the above mixed solution to 25°C in a water bath under the action of magnetic stirring;
[0026] (3) Disperse 3.31 g of reducing agent sodium borohydride and 0.021 g of dispersant sodium dodecylbenzenesulfonate in 50 mL of distilled water, and stir to disperse;
[0027] (4) Add the mixture in step (3) dropwise to the mixture in step (2) for 30 seconds, then continue to react at 25°C for 3 hours;
[0028] (5) The resulting suspension was centrifuged (10,000 rpm), washed twice with absolute ethanol and distilled water, and the resulting solid product was dispersed in 50 g of n-butanol and left to stand for 1 hour. XRD such as figure 1 As shown: the crystal phase of simple copper appears, no other copper oxides appear, and the surface has good oxidation r...
Embodiment 2
[0031] (1) Disperse 2.50 g of anhydrous cuprous acetate and 0.01 g of dispersant sodium dodecylbenzenesulfonate in 500 mL of distilled water, and obtain a mixed solution by magnetic stirring and ultrasonic dispersion;
[0032] (2) Heat the above mixed solution to 50°C in a water bath under the action of magnetic stirring;
[0033] (3) Disperse 1.56 g of sodium borohydride and 0.015 g of dispersant sodium dodecylbenzenesulfonate in 200 mL of distilled water, stir to disperse, and obtain a mixed solution;
[0034] (4) Add the mixture in step (3) dropwise to the mixture in step (2) for 90 seconds, then continue to react at 50°C for 3 hours;
[0035] (5) The resulting suspension was centrifuged (10,000 rpm), washed twice with absolute ethanol and distilled water, and the resulting solid product was dispersed in 20 g of tributyl phosphate and left to stand for 1 hour.
[0036] SEM detects the morphology and structure of copper nanoparticles, such as Figure 2A shown. The obtaine...
Embodiment 3
[0039] (1) Disperse 3.40 g of copper tartrate trihydrate and 0.10 g of dispersant sodium polyacrylate (molecular weight 3000) in 300 mL of distilled water, and obtain a mixed liquid by magnetic stirring and ultrasonic dispersion;
[0040] (2) Heat the above mixed solution to 75°C in a water bath under the action of magnetic stirring;
[0041] (3) Disperse 1.50 g of hydrazine hydrate and 0.24 g of dispersant sodium polyacrylate (molecular weight 3000) in 100 mL of distilled water, and stir to disperse;
[0042] (4) Add the mixture in step (3) dropwise to the mixture in step (2) for 50 seconds, then continue to react at 75°C for 3 hours;
[0043] (5) The resulting suspension was centrifuged (rotating at 10,000 rpm), washed twice with absolute ethanol and distilled water, and the resulting solid product was dispersed in 50 g of oleic acid and left to stand for 1 hour. SEM detects the morphological structure of the obtained nano-copper particles, such as Figure 2B shown. The o...
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