CN1373089A - Process for preparing anatase-phase nano TiO2 - Google Patents
Process for preparing anatase-phase nano TiO2 Download PDFInfo
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- CN1373089A CN1373089A CN 02115507 CN02115507A CN1373089A CN 1373089 A CN1373089 A CN 1373089A CN 02115507 CN02115507 CN 02115507 CN 02115507 A CN02115507 A CN 02115507A CN 1373089 A CN1373089 A CN 1373089A
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Abstract
A process for preparing anatase-phase nano-TiO2 includes dissolving cheap metatitanic acid in sulfuric acid to obtain the solution of titanyl sulfate, adding dropwise ammonium solution or the solution of sodium hydroxide, or the solution of ammonia and ammonium carbonate to obtain titanic acid, washing, drying and calcining. Its advantages are low cost, high high-temp stability, and high dispersity.
Description
Technical field
The present invention relates to anatase-phase nano TiO
2Preparation, belong to field of fine chemical, use present method can prepare at the high temperature nano-anatase phase TiO of stable existence still
2
Background technology
Nano-TiO
2Be meant the titanium dioxide product of grain-size less than 100 nanometers, because its particle is little, specific surface area is big, thereby higher chemically reactive is arranged, and is widely used in the Chemical Manufacture.Titanium dioxide has three kinds of crystal formations: sharp titanium, and rutile and brookite, the front is the kind of present widespread use for two kinds.Rutile is widely used in coating, makeup, and sunscreen, in the high-grade paint, its tinting strength is better than anatase octahedrite.Anatase octahedrite then is widely used in the chemical fibre delustring mutually, the photochemical catalysis decontamination, and photo-catalyst, its photochemidal activity is better than rutile TiO
2Anatase octahedrite is at cryostatic stabilization, generally just begin to transform but arrived high temperature to rutile at 600 ℃, 800 ℃ mostly with rutile mutually for mainly there being crystalline phase, and this crystal transition is a non-reversible process.In order to utilize the photochemical catalysis stain removal bactericidal of anatase octahedrite phase, need it is solidificated in the surface of glass and pottery and plays easy to clean and the antimicrobial characteristics, but with TiO
2Be solidificated in the surface of glass or pottery, particularly to pottery, its glaze temperature of fusion is generally more than 800 ℃, therefore requires at high-temperature stable and keeps nanocrystalline anatase octahedrite phase TiO
2Prepare TiO at present
2Method generally be to take TiCl
4Hydrolysis or thermal-flame method obtain, and are TiCl as the P25 product of Germany
4Flame method preparation, particle diameter is 30nm, anatase octahedrite and rutile mutually and save as sharp titanium: rutile=80: 20, TiCl
4The TiO of hydrolysis method preparation
2In the time of 700 ℃, begun to transform and granularity>100nm to rutile.The TiO of traditional sulfuric acid process preparation
2Still can keep most of anatase octahedrite phase at 800 ℃, but its particle diameter is bigger,, does not belong to nanocrystalline greater than 0.5 μ m.The sharp titanium nano-TiO of useful Prepared by Sol Gel Method
2, quality is better but cost is too high, only suitable prepared in laboratory and use.
Summary of the invention
It is lower and at the anatase-phase nano TiO of high-temperature stable that problem to be solved by this invention provides a kind of cost
2The preparation method.
Technical scheme provided by the invention is a kind of anatase-phase nano TiO
2The preparation method:
(1) uses H
2SO
4The dissolving metatitanic acid obtains titanyl sulfate;
(2) dilute sulphuric acid oxygen titanium solution concentration is at 0.05~0.5mol/L;
(3) use ammoniacal liquor, (NH
4)
2CO
3Regulate PH to 8-11 with the mixed solution of NaOH or ammoniacal liquor;
(4) the positive metatitanic acid of washing with 3% Ba (NO3), 2 mensuration to there not being SO
4 -
(5) calcination temperature is controlled at 500~800 ℃, and the treatment time is 1~2 hour;
Can obtain evenly by above-mentioned steps, disperse the TiO of 30~80nm of pure preferably sharp titanium phase
2
Outstanding feature of the present invention:
1. technology is simple, and raw material is cheap, is easy to scale operation.
2. temperature controllable obtains different big or small anatase octahedrite nano titanium oxides.
3. still be stable pure sharp titanium at 800 ℃ high temperature, and crystal grain only is the 80nm size.
Description of drawings:
Fig. 1 is the TEM photo of the present invention at 500 ℃ of calcining products obtained therefroms, magnification 33000;
Fig. 2 is the TEM photo of the present invention at 800 ℃ of calcining products obtained therefroms, magnification 33000;
Fig. 3 is a process flow sheet of the present invention.
Embodiment preparation flow of the present invention is as shown in Figure 3:
1, metatitanic acid and sulfuric acid are the commercially available prod, can obtain titanyl sulfate solution through heating for dissolving.
2, titanyl sulfate is diluted to 0.05~0.5mol/ and rises concentration, dropping ammonia then, 10% NaOH or ammoniacal liquor and 10-20% (NH
4)
2CO
3Mixed solution, slowly drip and stir, a large amount of CO will be arranged
2Gas produces, and regulates PH to 8-11.
3, with a large amount of water washing precipitations, to SO
4 -Clean.
4, the dry precipitation of cleaning is removed surface water.
5, intensification calcination, constant temperature in 500 ℃~800 ℃ intervals as required.The setting of warm area is relevant with nanocrystalline size, can obtain the TiO of about 30nm at 500 ℃ of constant temperature
2Crystal grain.Grow up at 800 ℃ of constant temperature crystal grain, about 80nm, but be all pure anatase octahedrite phase, Fig. 1 is the TEM photo of 500 ℃ product, the TEM photo when Fig. 2 is 800 ℃, and as seen from the figure, the dispersiveness of sample is better, uniform crystal particles.The X-ray diffraction figure main diffraction peak of 800 ℃ of constant temperature after 1 hour is: 25.28 ° (100), 48.09 ° (29), 37.85 ° (20), ° 53.90 (18), 55.06 ° (17) are the characteristic peaks of anatase octahedrite phase, and do not find the characteristic diffraction peak [27.45 ° (100)] of any rutile.
Embodiment 1: the dense H of metatitanic acid
2SO
4Dissolving obtains titanyl sulfate solution, and thin up is to the 0.4mol/ liter, and control drips 10%N down
aOH and 10% (NH
4)
2CO
3Mixing solutions, the limit edged stirs, and up to PH=8, drips off through 1 hour approximately, filtering reaction thing, and washing precipitation then is washed till 3% Ba (NO
3)
2Inspection is less than SO
4 -, 100 ℃ of dryings are sloughed surface water then, calcine 1 hour for 500 ℃, obtain product, and its big or small pattern is seen Fig. 1, and particle is even, and size is about 30nm.
Embodiment 2: the dense H of metatitanic acid
2SO
4Dissolving obtains titanyl sulfate solution, and thin up is controlled down the slowly ammoniacal liquor of dropping 10% and 20% (NH to the 0.06mol/ liter
4)
2CO
3Mixed solution, the limit edged stirred, and, dripped off filtering reaction thing, and washing precipitation then, the Ba (NO to 3% approximately up to PH=10 through 1 hour
3)
2Inspection is less than SO
4 -, 100 ℃ of dryings are sloughed surface water then, calcine 1 hour for 800 ℃, obtain product, and its big or small pattern is seen Fig. 2, and particle is even, and size is 50nm~80nm, its x-ray diffraction pattern is the characteristic peak of anatase octahedrite phase entirely, does not have the signal of any rutile.
Embodiment 3: the dense H of metatitanic acid
2SO
4Dissolving obtains titanyl sulfate solution, and thin up is to the 0.2mol/ liter, and control drips 10% ammoniacal liquor down, and the limit edged stirs, and up to PH=9, drips off through 1 hour approximately, and filtering reaction thing, and washing precipitation then is washed till 3% Ba (NO
3)
2Inspection is less than SO
4 -, 100 ℃ of dryings are sloughed surface water then, calcine 1 hour, and obtain product for 700 ℃.
Claims (1)
- A kind of anatase-phase nano TiO 2The preparation method, it is characterized in that:(1) uses H 2SO 4The dissolving metatitanic acid obtains titanyl sulfate;(2) dilute sulphuric acid oxygen titanium solution concentration is at 0.05~0.5mol/L;(3) use ammoniacal liquor, (NH 4) 2CO 3Regulate PH to 8-11 with the mixed solution of NaOH or ammoniacal liquor;(4) the positive metatitanic acid of washing is to there not being SO 4 -(5) calcination temperature is controlled at 500~800 ℃, and the treatment time is 1--2 hour;Can obtain evenly by above-mentioned steps, disperse the TiO of 30~80nm of pure preferably sharp titanium phase 2
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CNB021155070A CN1147431C (en) | 2002-02-01 | 2002-02-01 | Process for preparing anatase-phase nano TiO2 |
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CN1147431C CN1147431C (en) | 2004-04-28 |
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Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
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CN1330414C (en) * | 2005-09-20 | 2007-08-08 | 鞍山科技大学 | Method for preparing anatase type nano titanium dioxide photocatalyst |
CN100387526C (en) * | 2002-10-15 | 2008-05-14 | 北京化工大学 | Preparing method for nano titanium dioxide |
CN100448783C (en) * | 2004-12-09 | 2009-01-07 | 江苏大学 | Prepn process of anatase nanometer TiO2 powder |
CN100450935C (en) * | 2006-04-20 | 2009-01-14 | 华中师范大学 | Method for preparing size-controllable electronic grade anatase titania nanopowder |
CN100484880C (en) * | 2005-09-22 | 2009-05-06 | 中国科学院理化技术研究所 | Low-temperature crystallized nano titanium dioxide powder and synthesis method of sol |
CN104069843A (en) * | 2014-07-22 | 2014-10-01 | 苏州志佳电子科技有限公司 | Preparation method of titanium dioxide nanometer photocatalyst |
CN104923199A (en) * | 2015-06-09 | 2015-09-23 | 同济大学 | Preparation method for anatase TiO2 photocatalytic material with 1,100 DEG C high temperature stability |
CN107598090A (en) * | 2017-08-24 | 2018-01-19 | 合肥正明机械有限公司 | A kind of Steel Casting Risers coverture |
CN108070315A (en) * | 2017-11-28 | 2018-05-25 | 马鞍山蓝科再制造技术有限公司 | A kind of high-temp.-resisting fire-proof composite nano paint |
CN109482167A (en) * | 2018-11-09 | 2019-03-19 | 宁波水熊环保科技有限公司 | A kind of photochemical catalyst is spraying and preparation method thereof |
CN116153560A (en) * | 2023-02-28 | 2023-05-23 | 重庆大学 | Surface-modified titanium dioxide nano-sieve, preparation method thereof and application thereof in improving electrical strength of mineral insulating oil |
Families Citing this family (1)
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2002
- 2002-02-01 CN CNB021155070A patent/CN1147431C/en not_active Expired - Fee Related
Cited By (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100387526C (en) * | 2002-10-15 | 2008-05-14 | 北京化工大学 | Preparing method for nano titanium dioxide |
CN100448783C (en) * | 2004-12-09 | 2009-01-07 | 江苏大学 | Prepn process of anatase nanometer TiO2 powder |
CN1330414C (en) * | 2005-09-20 | 2007-08-08 | 鞍山科技大学 | Method for preparing anatase type nano titanium dioxide photocatalyst |
CN100484880C (en) * | 2005-09-22 | 2009-05-06 | 中国科学院理化技术研究所 | Low-temperature crystallized nano titanium dioxide powder and synthesis method of sol |
CN100450935C (en) * | 2006-04-20 | 2009-01-14 | 华中师范大学 | Method for preparing size-controllable electronic grade anatase titania nanopowder |
CN104069843A (en) * | 2014-07-22 | 2014-10-01 | 苏州志佳电子科技有限公司 | Preparation method of titanium dioxide nanometer photocatalyst |
CN104923199A (en) * | 2015-06-09 | 2015-09-23 | 同济大学 | Preparation method for anatase TiO2 photocatalytic material with 1,100 DEG C high temperature stability |
CN107598090A (en) * | 2017-08-24 | 2018-01-19 | 合肥正明机械有限公司 | A kind of Steel Casting Risers coverture |
CN108070315A (en) * | 2017-11-28 | 2018-05-25 | 马鞍山蓝科再制造技术有限公司 | A kind of high-temp.-resisting fire-proof composite nano paint |
CN109482167A (en) * | 2018-11-09 | 2019-03-19 | 宁波水熊环保科技有限公司 | A kind of photochemical catalyst is spraying and preparation method thereof |
CN116153560A (en) * | 2023-02-28 | 2023-05-23 | 重庆大学 | Surface-modified titanium dioxide nano-sieve, preparation method thereof and application thereof in improving electrical strength of mineral insulating oil |
CN116153560B (en) * | 2023-02-28 | 2024-01-19 | 重庆大学 | Surface-modified titanium dioxide nano-sieve, preparation method thereof and application thereof in improving electrical strength of mineral insulating oil |
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