CN101070186A - Method for preparing Zirconium dioxide nano powder - Google Patents
Method for preparing Zirconium dioxide nano powder Download PDFInfo
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- CN101070186A CN101070186A CN 200710057427 CN200710057427A CN101070186A CN 101070186 A CN101070186 A CN 101070186A CN 200710057427 CN200710057427 CN 200710057427 CN 200710057427 A CN200710057427 A CN 200710057427A CN 101070186 A CN101070186 A CN 101070186A
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Abstract
The invention is a kind of preparation method of nanometer powder of zirconium dioxide, it relates to zirconic oxide,it makes nanometer powder of zirconium dioxide using anodic oxidation, add solution of fluorid whose weight percentage concentrations is 0.5-1.0% into the reaction container, zirconium tablets is anode, platinum or graphite tablets is as cathode, the distance of anode and cathode is 1.5cm, adopt the direct current of 3.0- 3.5V to oxidize the anode, make them react for 30-60 minutes at room temperature, then take zirconium tablets out and absterge it with little water, and air it under the natural state or dry it at low temperature smaller than 105deg.C, then peel oxide equal and loose on surface of zirconium tablets off and crash it down, and then get cubical nanometer powder of zirconium dioxide of 10-100nm whose granule is equal. The method conquers the problems that the existing preparation method and craft of nanometer powder of zirconium dioxide is complex, the amount of waste liquid is great and it needs to be calcined at high temperature.
Description
Technical field
Technical scheme of the present invention belongs to the oxide compound of zirconium, specifically, relates to a kind of preparation method of Zirconium dioxide nano powder.
Background technology
Zirconium dioxide has excellent physics and chemical property, is widely used in pottery, refractory materials, catalyzer, support of the catalyst, piezoelectric element, the joints of optical fibre, gas sensor, solid fuel cell and thermal barrier coating.The particle diameter of zirconium dioxide powder is more little, and specific surface area is big more, and the surface energy of powder increases severely, and can improve its application performance.For example, the sintering activating energy of Zirconium dioxide nano powder is less, and sintering densification speed is accelerated, and sintering temperature is reduced, and sintering time shortens.
The main method of preparation zirconium dioxide powder has the precipitator method, sol-gel method, metal alkoxide method, reverse micro emulsion method at present.CN 1169958A discloses a kind of preparation method of pulverulent zirconium dioxide, and zirconium compounds is dissolved in the aqueous formic acid, is spray dried to powder, 850-1350 ℃ calcine product; CN1260324A discloses a kind of preparation method of zirconium dioxide, with ZrOCl
2The aqueous solution is added drop-wise to and makes Zr (OH) in the precipitation agent
4Hydrogel is with Zr (OH)
4Hydrogel thorough washing after drying, roasting get product; CN 1482065A discloses a kind of hydrolysis Zircosol ZN and prepares Zirconium dioxide nano powder technology, adds carbon nanotube in the aqueous solution of concentrated nitric acid oxygen zirconium, refluxes, boils, and oven dry, roasting get product; CN 1733611A discloses a kind of manufacture method of Zirconium dioxide nano powder material, zirconium saline solution and ammonia aqueous solution are joined dispersion and emulsion in the organic solution respectively, then two emulsions are mixed, ultra-sonic dispersion, distillation, wash head product, head product through cryogenic freezing and 600-800 ℃ calcine product.These methods generally will pass through liquid phase reaction, separation, washing, oven dry, reach the high-temperature calcination flow process, and technology is comparatively complicated, and energy consumption is big; Particularly separation, washing procedure because the intermediate particle diameter is very little, even are gel, and isolating difficulty and cost are improved, and the waste liquid amount that washing produces is big, and remaining foreign ion is many, cause the product purity reduction.
Summary of the invention
Technical problem to be solved by this invention is: a kind of preparation method of Zirconium dioxide nano powder is provided, and it is an anonizing, and this method has overcome the shortcoming that existing zirconium dioxide powder preparation method technical matters complexity, waste liquid amount are big, need high-temperature calcination.
The present invention solves this technical problem the technical scheme that is adopted: adopt anonizing to prepare Zirconium dioxide nano powder, concrete steps are: the adding weight percent concentration is 0.5～1.0% fluoride aqueous solution in reaction vessel, the zirconium sheet is made anode, platinized platinum or graphite flake are made negative electrode, anode and cathode spacing are from being 1.5cm, adopt 3.0～3.5V direct current to carry out anodic oxidation, room temperature reaction 30～60 minutes, take out the zirconium sheet then, wash with less water, under state of nature, dry again or oven dry under＜105 ℃ low temperature, then evenly with zirconium sheet surface, loose oxide compound is peeled off, pulverize, promptly make 10～100nm, uniform cube of phase Zirconium dioxide nano powder of particle diameter.
Fluorochemical among the above-mentioned preparation method is a kind of or two or more mixture in Sodium Fluoride, Potassium monofluoride, Neutral ammonium fluoride, the hydrogen fluoride.
Among the above-mentioned preparation method, the purity of used zirconium sheet is not less than 99.9%.
The invention has the beneficial effects as follows:
(1) substantive distinguishing features of the present invention and marked improvement are, at ambient temperature, adopt anonizing to prepare Zirconium dioxide nano powder, the Zirconium dioxide nano powder that reaction generates is stable cube phase, attached to zirconium sheet surface (seeing accompanying drawing), can directly wash with water, not have filtration, calcination process, technology is simple, with short production cycle, energy consumption is low, and is pollution-free, is easy to suitability for industrialized production.
(2) innovative point of the present invention is: with the high purity metal zirconium is raw material, the product purity height; Other method is generally made raw material with the compound of zirconium.Metal zirconium generates the zirconium dioxide molecule with water molecule reaction under electric field action, the zirconium dioxide molecule mutually combines, and becomes zirconium dioxide nanoparticles at zirconium sheet surface aggregation, peels off the later zirconium sheet of product and can reuse, until complete reaction.
(3) another innovative point of the present invention is: in 0.5～1.0% fluoride aqueous solution, adopt 3.0～3.5V direct current to carry out anodic oxidation reactions, the Zirconium dioxide nano powder that zirconium sheet surface is generated is loose, and product was both easily peeled off, and easily pulverized again.
(4) the present invention is at room temperature reaction, and with the reaction times prolongation, the zirconium dioxide amount that zirconium sheet surface generates increases, and conductive capability descends, and the suitable reactions time is 30～60 minutes.
In a word, the inventive method just can be prepared 10～100nm, uniform cube of phase Zirconium dioxide nano powder of particle diameter by adjusting fluorochemical composition and concentration, anodic oxidation voltage and reaction times.
Description of drawings
The present invention is further described below in conjunction with drawings and Examples.
Fig. 1 is the in kind photo of Zirconium dioxide nano powder at the attachment state on zirconium sheet surface.
Embodiment
Fig. 1 shows that the stable cube phase Zirconium dioxide nano powder that is made by the following example of the present invention is even on zirconium sheet surface, loosens and adhere to, and both can directly wash with water, is beneficial to again and peels off, pulverizes operation.
Embodiment 1
The adding weight percent concentration is 0.5% aqueous hydrogen fluoride solution in reaction vessel, the zirconium sheet is made anode, and platinized platinum is made negative electrode, and anode and cathode spacing are from being 1.5cm, adopt the 3.5V direct current to carry out anodic oxidation, room temperature reaction 30 minutes takes out the zirconium sheet then, washs with less water, under state of nature, dry, then even, the loose oxide compound in zirconium sheet surface is peeled off, pulverized, promptly make Zirconium dioxide nano powder.
Embodiment 2
The adding weight percent concentration is 1.0% ammonium fluoride aqueous solution in reaction vessel, the zirconium sheet is made anode, and graphite flake is made negative electrode, and anode and cathode spacing are from being 1.5cm, adopt the 3.0V direct current to carry out anodic oxidation, room temperature reaction 50 minutes takes out the zirconium sheet then, washs with less water, in＜105 ℃ of oven dry, then even, the loose oxide compound in zirconium sheet surface is peeled off, pulverized, promptly make Zirconium dioxide nano powder.
Embodiment 3
The adding weight percent concentration is 0.8% sodium fluoride aqueous solution in reaction vessel, the zirconium sheet is made anode, and platinized platinum is made negative electrode, and anode and cathode spacing are from being 1.5cm, adopt the 3.3V direct current to carry out anodic oxidation, room temperature reaction 60 minutes takes out the zirconium sheet then, washs with less water, in＜105 ℃ of oven dry, even, the loose oxide compound in zirconium sheet surface is peeled off, pulverized, promptly make Zirconium dioxide nano powder.
Embodiment 4
Except that replacing the Sodium Fluoride with Potassium monofluoride, other make Zirconium dioxide nano powder thus all with embodiment 3.
Embodiment 5
Preparation contains the aqueous solution that weight percent concentration is the Sodium Fluoride of 0.3% Neutral ammonium fluoride and 0.3%, adds in the reaction vessel, and the zirconium sheet is made anode, platinized platinum is made negative electrode, anode and cathode spacing adopt the 3.2V direct current to carry out anodic oxidation, room temperature reaction 40 minutes from being 1.5cm, take out the zirconium sheet then, with the less water washing, under state of nature, dry, even, the loose oxide compound in zirconium sheet surface is peeled off, pulverize, promptly make Zirconium dioxide nano powder.
Embodiment 6
Except that replacing the Sodium Fluoride with Potassium monofluoride, other make Zirconium dioxide nano powder thus all with embodiment 5.
Embodiment 7
Except that replacing the Sodium Fluoride with hydrogen fluoride, other make Zirconium dioxide nano powder thus all with embodiment 5.
Embodiment 8
It is 0.6% the Neutral ammonium fluoride and 0.3% the hydrofluoric aqueous solution that preparation contains weight percent concentration, adds in the reaction vessel, and the zirconium sheet is made anode, graphite flake is made negative electrode, anode and cathode spacing adopt the 3.2V direct current to carry out anodic oxidation, room temperature reaction 50 minutes from being 1.5cm, take out the zirconium sheet then, with the less water washing,, even, the loose oxide compound in zirconium sheet surface is peeled off in＜105 ℃ of oven dry, pulverize, promptly make Zirconium dioxide nano powder.
Embodiment 9
It is 0.3% Neutral ammonium fluoride, 0.3% Sodium Fluoride and 0.3% the hydrofluoric aqueous solution that preparation contains weight percent concentration, adds in the reaction vessel, and the zirconium sheet is made anode, platinized platinum is made negative electrode, anode and cathode spacing adopt the 3.0V direct current to carry out anodic oxidation, room temperature reaction 30 minutes from being 1.5cm, take out the zirconium sheet then, with the less water washing, under state of nature, dry, even, the loose oxide compound in zirconium sheet surface is peeled off, pulverize, promptly make Zirconium dioxide nano powder.
Embodiment 10
Except that replacing the Sodium Fluoride with Potassium monofluoride, other make Zirconium dioxide nano powder thus all with embodiment 9.
Embodiment 11
Preparation contains the aqueous solution that weight percent concentration is the Potassium monofluoride of 0.3% Neutral ammonium fluoride, 0.3% Sodium Fluoride and 0.3%, adds in the reaction vessel, and the zirconium sheet is made anode, platinized platinum is made negative electrode, anode and cathode spacing adopt the 3.4V direct current to carry out anodic oxidation, room temperature reaction 60 minutes from being 1.5cm, take out the zirconium sheet then, with the less water washing,, even, the loose oxide compound in zirconium sheet surface is peeled off in＜105 ℃ of oven dry, pulverize, promptly make Zirconium dioxide nano powder.
Embodiment 12
It is 0.2% Neutral ammonium fluoride, 0.2% Sodium Fluoride, 0.2% Potassium monofluoride and 0.2% the hydrofluoric aqueous solution that preparation contains weight percent concentration, adds in the reaction vessel, and the zirconium sheet is made anode, graphite flake is made negative electrode, anode and cathode spacing adopt the 3.0V direct current to carry out anodic oxidation, room temperature reaction 60 minutes from being 1.5cm, take out the zirconium sheet then, with the less water washing,, even, the loose oxide compound in zirconium sheet surface is peeled off in＜105 ℃ of oven dry, pulverize, promptly make Zirconium dioxide nano powder.
The purity of used zirconium sheet all is not less than 99.9% in the foregoing description.
Claims (3)
1. the preparation method of Zirconium dioxide nano powder, it is characterized in that: adopt anonizing to prepare Zirconium dioxide nano powder, concrete steps are: the adding weight percent concentration is 0.5～1.0% fluoride aqueous solution in reaction vessel, the zirconium sheet is made anode, platinized platinum or graphite flake are made negative electrode, anode and cathode spacing are from being 1.5cm, adopt 3.0～3.5V direct current to carry out anodic oxidation, room temperature reaction 30～60 minutes, take out the zirconium sheet then, wash with less water, under state of nature, dry again or oven dry under＜105 ℃ low temperature, then evenly with zirconium sheet surface, loose oxide compound is peeled off, and pulverizes, and promptly makes 10～100nm, uniform cube of phase Zirconium dioxide nano powder of particle diameter.
2. according to the preparation method of the described Zirconium dioxide nano powder of claim 1, it is characterized in that: the fluorochemical among the above-mentioned preparation method is a kind of or two or more mixture in Sodium Fluoride, Potassium monofluoride, Neutral ammonium fluoride, the hydrogen fluoride.
3. according to the preparation method of the described Zirconium dioxide nano powder of claim 1, it is characterized in that: used zirconium sheet purity is not less than 99.9% among the above-mentioned preparation method.
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| CNB2007100574275A CN100551830C (en) | 2007-05-23 | 2007-05-23 | The preparation method of Zirconium dioxide nano powder |
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102068989A (en) * | 2010-12-02 | 2011-05-25 | 河北工业大学 | Method for preparing ZrO2 nanotube supported copper catalyst |
| CN106470958A (en) * | 2014-07-14 | 2017-03-01 | 里弗雷克特里知识产权两合公司 | Refractory product, the purposes of zirconium dioxide, zirconium dioxide, be used for the method manufacturing refractory product and the refractory product being produced from |
| CN108609652A (en) * | 2018-06-13 | 2018-10-02 | 李春月 | A method of preparing Zirconium dioxide nano powder using fused salt |
-
2007
- 2007-05-23 CN CNB2007100574275A patent/CN100551830C/en not_active Expired - Fee Related
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN102068989A (en) * | 2010-12-02 | 2011-05-25 | 河北工业大学 | Method for preparing ZrO2 nanotube supported copper catalyst |
| CN102068989B (en) * | 2010-12-02 | 2012-10-03 | 河北工业大学 | Method for preparing ZrO2 nanotube supported copper catalyst |
| CN106470958A (en) * | 2014-07-14 | 2017-03-01 | 里弗雷克特里知识产权两合公司 | Refractory product, the purposes of zirconium dioxide, zirconium dioxide, be used for the method manufacturing refractory product and the refractory product being produced from |
| CN108609652A (en) * | 2018-06-13 | 2018-10-02 | 李春月 | A method of preparing Zirconium dioxide nano powder using fused salt |
| CN108609652B (en) * | 2018-06-13 | 2020-02-07 | 李春月 | Method for preparing zirconium dioxide nano powder by using molten salt |
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| CN100551830C (en) | 2009-10-21 |
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Granted publication date: 20091021 Termination date: 20120523 |