CN1618765A - Preparation method of niobium doped barium sodium titanate nano-powder - Google Patents
Preparation method of niobium doped barium sodium titanate nano-powder Download PDFInfo
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- CN1618765A CN1618765A CN 200410073215 CN200410073215A CN1618765A CN 1618765 A CN1618765 A CN 1618765A CN 200410073215 CN200410073215 CN 200410073215 CN 200410073215 A CN200410073215 A CN 200410073215A CN 1618765 A CN1618765 A CN 1618765A
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Abstract
A process for preparing the Nb-doped barium titanate nanoparticles by sol-gel method includes mixing butyl titanate with acetic acid or alcohol to obtain the solution of butyl titanate, adding the solution of barium acetate to it, using acetic acid to regulate pH=3.5-4.5, adding H3[Nb(O2)4] solution, gelatinizing at 40-80 deg.C, drying, calcining at 700-1200 deg.C for 0.5-4 hr, and ball grinding.
Description
Technical field
The present invention relates to a kind of preparation method of niobium doped barium sodium titanate nano-powder, particularly a kind of method for preparing niobium doped barium sodium titanate nano-powder by sol-gel method.
Background technology
Barium titanate based ceramic is widely used as the dielectric materials of laminated ceramic capacitor (MLCC) because of having higher dielectric constant and environmentally safe.But the dielectric temperature less stable of pure barium titanate pottery, be that its specific inductivity is very big with the environment for use variation of temperature, and at room temperature specific inductivity is less, therefore need control its microtexture by other element that mixes, and improves its specific inductivity and improves its dielectric temperature stability; The more important thing is that the thin brilliant thin layer MLCC material of preparation must adopt the adulterated barium phthalate base nano-powder material of multiple composition, to satisfy the demand for development of MLCC miniaturization day by day, high capacity.In many properties-correcting agent, Nb
2O
5In Nb
5+Replace BaTiO
3Ti in the lattice
4+, can obviously suppress grain growth, and can improve the dielectric temperature stability of barium titanate based ceramic greatly when composite mixed, thereby obtain extensive studies and application with rare earth, cobalt etc.Rare earth and cobalt element with which kind of method mix all to be easy to realize, but Nb
5+Doping but be difficult for to realize.Because the singularity of high price niobium compound chemical property is mixed the niobium mode at present and mostly is the solid phase doping, promptly earlier makes the pure barium titanate powder by solid phase method, hydrothermal synthesis method or chemical precipitation method etc., then with oxide compound (Nb
2O
5) form mixes, need to realize mix (Mitic V.V, Mitrovic I., The influence of Nb through technologies such as ball milling, calcinings
2O
5On BaTiO
3Ceramics dielectricproperties, Journal of the European Ceramic Society, 2001,21:2693-2696; Brzozowski.E, Castro.M.S, Foschini.C.R, et al, Secondary phase in Nb-doped BaTiO
3Ceramics.Ceramics International, 2002,28:773-777).This adulterating method, to the purity and the granularity requirements strictness of raw material, and easily the generation doping is inhomogeneous, influences the stability of product.Utilize sol-gel method in parent colloidal sol, to add pure niobium and be expected to make the Barium Titanate nano-powder material of mixing niobium, but pure niobium costs an arm and a leg, and be difficult for storing and transportation, in preparation process, also need waterless operation, complex process, cost is higher.If the water-soluble cpds substituted alcohols niobium with the lower niobium of price then can reduce its manufacturing cost greatly, but because Nb
2O
5Chemical stability good, be difficult to make and can contain the niobium water-soluble cpds with titanium, barium coexistence form colloidal sol.
Summary of the invention
The purpose of this invention is to provide a kind of method for preparing even niobium doped barium sodium titanate nano-powder, this method is with H
3[Nb (O
2)
4] solution replaces expensive pure niobium, prepares the niobium doped barium sodium titanate nano-powder material by sol-gel method, overcomes the prior art inhomogeneous or expensive deficiency of mixing.
The step of preparation process of the present invention of realizing above-mentioned purpose is as follows successively:
A. with butyl (tetra) titanate and acetic acid, ethanol mixed butyl (tetra) titanate solution;
B. barium acetate solution being added in the butyl (tetra) titanate solution, is 3.5-4.5 with acetic acid regulator solution pH value, adds H then
3[Nb (O
2)
4] solution, 40-80 ℃ of gelation, the dry dry gel powder that gets;
C. dry gel powder is incubated 700～1200 ℃ of roastings, and ball milling gets the pre-burning powder.
Among the above-mentioned processing step a, butyl (tetra) titanate and acetic acid, ethanol mixed butyl (tetra) titanate solution, both can stirring and dissolving, also can help dissolving with ultra-sonic dispersion; Ethanol occurs as solvent, and the adding of acetic acid mainly is the hydrolysis and the polymerization velocity of control butyl (tetra) titanate, and therefore, its add-on makes butyl (tetra) titanate not decompose at least and is advisable.
Among the above-mentioned processing step b, H
3[Nb (O
2)
4] solution can obtain by three kinds of methods: 1., be dissolved in H at last with Niobium Pentxoxide and the reaction of potassium pyrosulfate heating and melting
2O
2Make; 2. H
3[Nb (O
2)
4] solution is by Niobium Pentxoxide and salt of wormwood reacting by heating, makes potassium niobate, through the oxalic acid dissolving, ammonia precipitation process makes Nb (OH) then
5, be dissolved in H afterwards
2O
2Make; 3. H
3[Nb (O
2)
4] solution is to make Nb (OH) by the columbium pentachloride hydrolysis
5, be dissolved in H afterwards
2O
2Make.
Among the above-mentioned processing step b, butyl (tetra) titanate and barium acetate amount of substance ratio can change between 0.95～1.05.
In order to obtain the good niobium doped barium sodium titanate nano-powder of phase composite and microstructure, the content of titanium relatively, the add-on of niobium is 0.1～10.0mol%, H
3[Nb (O
2)
4] content of niobium is determined by weighting method in the solution; Dry gel powder roasting soaking time 0.5～4h gets final product.
Use traditional solid phase doping method, be difficult to obtain the high and good niobium doped barium sodium titanate nano-powder material of distributing homogeneity of reactive behavior, also just be unfavorable for the manufacturing of the thin brilliant stupalith of miniaturization MLCC thin layer.The present invention is with water-soluble H
3[Nb (O
2)
4] replace expensive pure niobium (as the ethanol niobium) as mixing niobium component, adopt the sol-gel method preparation evenly to mix the Barium Titanate nano-powder of niobium, raw material is easy to get, equipment is simple, technology is succinct, with low cost, be easy to suitability for industrialized production.
The method for preparing niobium doped barium sodium titanate nano-powder of the present invention has the following advantages and positively effect:
1, uses H
3[Nb (O
2)
4] solution replaces pure niobium, compares with pure niobium, greatly reduces the preparation cost of sol-gel method.
2, the niobium doped barium sodium titanate nano-powder that makes of the method for the invention can be used for preparing thin brilliant thin layer barium phthalate base MLCC material, also can be used for PTC thermal sensitive ceramic material etc.
3, by the Nb-doped barium titanate precursor sol and the gel of the method for the invention preparation, make the chemical constitution of Nb-doped barium titanate powder even, the purity height, titanium barium than and mix the niobium amount and be easy to control.
4, the method for the invention makes water, acetic acid and ethanol as solvent in preparation process, production safety, and operating environment requires simple.
5, the Nb-doped barium titanate nanocrystalline powder that obtains of preparation method of the present invention helps reducing the sintering temperature of pottery, thereby has reduced energy consumption and production cost.
Description of drawings
The XRD figure spectrum of Fig. 1 sample 1-4
The TEM photo of Fig. 2 sample 1-4
The XRD figure spectrum of Fig. 3 sample 5-8
The TEM photo of Fig. 4 sample 5-8
Embodiment
The analysis of the Japanese D/MAX-3CX of company diffractometer of science is adopted in the phase composite of Nb-doped barium titanate powder; The microstructure of Nb-doped barium titanate powder is by the H-600 of HIT type transmission electron microscope observing.
Example 1:
(1) taking by weighing potassium pyrosulfate 10 grams at 1: 10 by Niobium Pentxoxide and potassium pyrosulfate mass ratio places mortar to grind, add 1 gram Niobium Pentxoxide, be transferred in the crucible after grinding evenly, be heated to melt temperature (300～320 ℃) reaction 50min after, naturally cooling gets frit I.
(2) the hot oxalic acid solution (about 30ml) of 8% (massfraction) is poured in the crucible, dissolved above-mentioned frit I.After leaving standstill, remove by filter insolubles, in filtrate, drip the ammoniacal liquor of 14% (massfraction) while stirring, regulating pH is about 10, after suitably heating, and suction filtration, elder generation washs 3～4 times with 3% thermal chlorination ammonium solution (or ammonium nitrate solution), is washed till no SO with hot distilled water then
4 2-, Cl
-(use BaCl respectively
2Solution and AgNO
3The solution check), obtain Nb (OH)
5Precipitation II.
(3) gained is precipitated II and be dissolved in 5% hot oxalic acid solution, drip 14% ammoniacal liquor once more when stirring, produce precipitation, circulation 2-3 time is not contained the Nb (OH) of other foreign ion
5The about 2.7g of solid precipitation adds entry 5ml, H
2O
210ml, the H of clear
3[Nb (O
2)
4] solution III.
(5) adopt H in the gravimetric determination solution III
3[Nb (O
2)
4] be equivalent to Nb
2O
5Content be 0.047g/ml.
(6) in butyl (tetra) titanate: the ratio (amount of substance mark) of barium acetate=1: 1 takes by weighing the 21.8898g butyl (tetra) titanate, add 13ml Glacial acetic acid and 6ml dehydrated alcohol, add the aqueous solution that contains the 16.4289g barium acetate when stirring, ultra-sonic dispersion makes its thorough mixing even, regulate pH=4 with acetic acid, under agitation drip the above-mentioned niobium solution of 3.67ml then, behind the stirring 30min, 45 ℃ of gelations, 70 ℃ of dryings, again with them respectively 900,1000,1100, ball milling 12h behind 1200 ℃ of following roasting 2h obtains mixing the Barium Titanate nano-powder material of niobium 1.0mol%, is designated as sample 1 respectively, sample 2, sample 3 and sample 4.
All can access cubic phase barium titanate under the different as can be seen from Figure 1 calcined temperatures, its diameter of particle calculates between 27nm～30nm according to the Scherrer formula according to XRD figure spectrum, and the particle diameter that obtains from the TEM photo of Fig. 2 is between 40nm～2 μ m.
Example 2:
(1) makes the aqueous solution of niobium according to the method for embodiment 1;
(2) in butyl (tetra) titanate: the ratio (amount of substance mark) of barium acetate=1: 1 takes by weighing four parts of 21.8898g butyl (tetra) titanates, respectively add 13ml Glacial acetic acid and 6ml dehydrated alcohol under the room temperature, under agitation drip the aqueous solution that contains the 16.4289g barium acetate respectively, mix, regulate pH=4 with acetic acid, adding volume respectively when stirring is 3.67,11.25,19.14 and the concentration of 40.42ml is 0.047g/ml niobium solution, after stirring 30min, 65 ℃ of gelations, 70 ℃ of dryings, again they are calcined 2h down at 900 ℃, ball milling 12h, obtain mixing the niobium amount and be respectively 1.0,3.0,5.0 the Barium Titanate nano-powder material with 10.0mol% is designated as sample 5 respectively, sample 6, sample 7 and sample 8.
By the XRD figure of Fig. 3 spectrum as seen, the pre-burning powder is a cubic phase barium titanate, its diameter of particle according to the XRD figure spectrum according to the calculating of Scherrer formula between 20nm～31nm, the particle diameter that obtains from the TEM photo of Fig. 4 is between 25nm～40nm.
Claims (7)
1, a kind of preparation method of niobium doped barium sodium titanate nano-powder, its preparation technology in turn includes the following steps:
A. with butyl (tetra) titanate and acetic acid, ethanol mixed butyl (tetra) titanate solution;
B. barium acetate solution being added in the butyl (tetra) titanate solution, is 3.5-4.5 with acetic acid regulator solution pH value, adds H then
3[Nb (O
2)
4] solution, 40-80 ℃ of gelation, the dry dry gel powder that gets;
C. dry gel powder is incubated 700～1200 ℃ of roastings, and ball milling gets the pre-burning powder.
2, the preparation method of niobium doped barium sodium titanate nano-powder according to claim 1 is characterized in that: with respect to the content of titanium, the add-on of niobium is 0.1～10.0mol%, H
3[Nb (O
2)
4] content of niobium is determined by weighting method in the solution.
3, the preparation method of niobium doped barium sodium titanate nano-powder according to claim 1 and 2 is characterized in that: H
3[Nb (O
2)
4] solution is with the reaction of Niobium Pentxoxide and potassium pyrosulfate heating and melting, is dissolved in H at last
2O
2Make.
4, the preparation method of niobium doped barium sodium titanate nano-powder according to claim 1 and 2 is characterized in that: H
3[Nb (O
2)
4] solution is by Niobium Pentxoxide and salt of wormwood reacting by heating, makes potassium niobate, through the oxalic acid dissolving, ammonia precipitation process makes Nb (OH) then
5, be dissolved in H afterwards
2O
2Make.
5, the preparation method of niobium doped barium sodium titanate nano-powder according to claim 1 and 2 is characterized in that: H
3[Nb (O
2)
4] solution is to make Nb (OH) by the columbium pentachloride hydrolysis
5, be dissolved in H afterwards
2O
2Make.
6, the preparation method of niobium doped barium sodium titanate nano-powder according to claim 1 and 2 is characterized in that: dry gel powder roasting insulation 0.5～4h.
7, the preparation method of niobium doped barium sodium titanate nano-powder according to claim 1 is characterized in that: butyl (tetra) titanate is 0.95～1.05 with barium acetate amount of substance ratio.
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| CN1272280C CN1272280C (en) | 2006-08-30 |
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Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101935210A (en) * | 2010-08-29 | 2011-01-05 | 青岛理工大学 | Method for synthesizing lithium-niobium-titanium microwave medium ceramic powder by Ti gel |
| CN102276254A (en) * | 2011-06-01 | 2011-12-14 | 天津大学 | Method for modifying barium strontium titanate material through sol-gel doping technology |
| CN102603288A (en) * | 2011-12-05 | 2012-07-25 | 合肥工业大学 | Lead-free piezoelectric film material and preparation method thereof |
| CN102963928A (en) * | 2012-11-12 | 2013-03-13 | 西北大学 | Barium zirconate titanate based Y5V powder material and preparation method thereof |
| CN103980859A (en) * | 2014-05-28 | 2014-08-13 | 天津大学 | Silver-doped barium titanate nanometre wave-absorbing material and preparation method thereof |
| CN106751780A (en) * | 2016-12-26 | 2017-05-31 | 东莞市佳乾新材料科技有限公司 | For the daiamid composition and manufacture method of piezoelectric |
-
2004
- 2004-11-02 CN CN 200410073215 patent/CN1272280C/en not_active Expired - Fee Related
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN101935210A (en) * | 2010-08-29 | 2011-01-05 | 青岛理工大学 | Method for synthesizing lithium-niobium-titanium microwave medium ceramic powder by Ti gel |
| CN101935210B (en) * | 2010-08-29 | 2014-11-05 | 青岛理工大学 | Method for synthesizing lithium-niobium-titanium microwave medium ceramic powder by Ti gel |
| CN102276254A (en) * | 2011-06-01 | 2011-12-14 | 天津大学 | Method for modifying barium strontium titanate material through sol-gel doping technology |
| CN102276254B (en) * | 2011-06-01 | 2013-04-03 | 天津大学 | Method for modifying barium strontium titanate material through sol-gel doping technology |
| CN102603288A (en) * | 2011-12-05 | 2012-07-25 | 合肥工业大学 | Lead-free piezoelectric film material and preparation method thereof |
| CN102963928A (en) * | 2012-11-12 | 2013-03-13 | 西北大学 | Barium zirconate titanate based Y5V powder material and preparation method thereof |
| CN102963928B (en) * | 2012-11-12 | 2016-04-13 | 西北大学 | Barium zirconate titanate-based Y5V powder body material and preparation method thereof |
| CN103980859A (en) * | 2014-05-28 | 2014-08-13 | 天津大学 | Silver-doped barium titanate nanometre wave-absorbing material and preparation method thereof |
| CN106751780A (en) * | 2016-12-26 | 2017-05-31 | 东莞市佳乾新材料科技有限公司 | For the daiamid composition and manufacture method of piezoelectric |
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| Publication number | Publication date |
|---|---|
| CN1272280C (en) | 2006-08-30 |
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