CN1473791A - Core-shell structure nano titanium serial composition and its preparing method - Google Patents
Core-shell structure nano titanium serial composition and its preparing method Download PDFInfo
- Publication number
- CN1473791A CN1473791A CNA031322174A CN03132217A CN1473791A CN 1473791 A CN1473791 A CN 1473791A CN A031322174 A CNA031322174 A CN A031322174A CN 03132217 A CN03132217 A CN 03132217A CN 1473791 A CN1473791 A CN 1473791A
- Authority
- CN
- China
- Prior art keywords
- mixture
- nano
- nano titanium
- titanium
- weighing
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Images
Landscapes
- Inorganic Compounds Of Heavy Metals (AREA)
Abstract
The present invention discloses serial nano titanium compositions in core-shell structure and their preparing process. Through homogeneous precipitation process, the precipitation reaction and chemical processing are completed in one step. Transmissive electronic microscope detection shows that the initial particle has size of 30-80 nm; X-ray diffraction detection shows the crystal grain size of 10-30 nm; X-ray electronic energy spectrum analysis shows the oxide of Si or Al is concentrated mainly on the surface shell layer; and precipitation performance analysis shows that the serial nano titanium compositions in core-shell structure have slow precipitation speed in deionized water and have dispersivity greatly superior to nano titania prepared in the same process.
Description
Technical field
The present invention relates to a kind of nuclear shell structured nano-titanium is mixture and preparation method thereof.
Background technology
Nano titanium oxide is owing to the particulate super-refinement, and produced the not available characteristic of many macrobead titanium dioxide: (1) specific surface area is big; (2) surfactivity can be high; (3) ultravioletlight screening rate height; (4) magnetic is strong; (5) heat conductance is good.Thereby be able to widespread use in fields such as photochemical catalysis, functional high molecule material, transmitter, support of the catalyst.Along with the expansion of nano titanium oxide Application Areas, the nano titanium oxide of low, the good dispersity of processability excellence, cost how becomes the focus and the difficult point in research and development field.Various corresponding preparation method are arisen at the historic moment as gas phase hydrolysis method, vapour phase oxidation process, peptisation, sol-gel method, hydrothermal synthesis method, liquid-phase precipitation method etc., nano titanium oxide purity height, little, the good dispersity of particle diameter that gas phase hydrolysis method and gaseous oxidation are prepared, at high temperature moment finishes but react, equipment and technology controlling and process are had relatively high expectations, be difficult to industrialization promotion; Nano titanium oxide dispersiveness, the transparency height of peptisation preparation, but technical process is long, cost is higher; The sol-gel method cost is higher, relatively is suitable for in-situ compositing and prepares nanometer titanium dioxide composite material; The nano titanium oxide particle diameter of Hydrothermal Preparation is little, it is few to be evenly distributed, to reunite, but equipment requirements is high pressure resistant, high temperature, and cost is higher; Comparatively speaking, it is lower that liquid-phase precipitation method prepares the nano titanium oxide cost, and technology is simple relatively, and processing condition are easy to control, are suitable for industrialization promotion, and the CONTROL PROCESS condition can be controlled size of particles and distribution.Chinese patent CN1192992 discloses a kind of method of Preparation by Uniform Precipitation nano titanium oxide, and technology is simple relatively, is easy to industrialization.
Above-mentioned numerous technological method can prepare the less nano titanium oxide of particle diameter, but improves dispersing nanometer titanium dioxide and dispersion stabilization, particularly prevents the secondary aggregation in the application process, still is technological difficulties.For cohesion and the scattering problem that solves nano titanium oxide, bring into play the excellent properties of nano titanium oxide better, adopt the surface-treated method usually, improve dispersing nanometer titanium dioxide.
Chinese patent CN1296917 discloses a kind of nano titanium oxide surface-treated method, is after titanic oxide shaping, adopts tensio-active agent, carries out hydrophilic respectively and the oleophylic processing, has improved dispersing nanometer titanium dioxide.Chinese patent CN1328962 discloses a kind of method for preparing nano titanium oxide, is to carry out inorganic coating to handle after washing and filtering, improves dispersing nanometer titanium dioxide and weathering resistance.Chinese patent CN1296917 discloses a kind of preparation method of uniform compound monodispersed nm-class spherical TiO 2 particles, is to be raw material with the titanic acid ester, adds silicon-dioxide in polar organic solvent, the nano titanium oxide of the good dispersity that preparation size is controlled.
Nano titanium oxide surface-treated method also has a lot, as high power treatment method, mechanochemical reaction, surface grafting method etc.Its major part is to adopt the method for aftertreatment, and the technology circuit is longer, and the prepared nano titanium oxide of the method for aftertreatment, and many physical indexs all depend on its former process, thereby the post-processing function performance is subjected to restriction to a certain degree.
Summary of the invention
The objective of the invention is: it is mixture and preparation method thereof that a kind of nuclear shell structured nano-titanium is provided, and adopts sluggish precipitation, and a step is finished precipitin reaction and chemical treatment, and the dispersed stable nuclear shell structured nano-titanium of preparation is a mixture.
Technical scheme of the present invention is: a kind of nuclear shell structured nano-titanium is a mixture, and its component is:
TiO
2:90-99%
SiO
2Or Al
2O
3Or SiO
2+ Al
2O
3: 1-10%.
The particle diameter of mixture is 30-80nm.
A kind of nuclear shell structured nano-titanium is the preparation method of mixture, adopts even coprecipitation method, is raw material with the metatitanic acid, and urea is precipitation agent, with Al
2(SO
4)
3Or Na
2SiO
3Or Al
2(SO
4)
3+ Na
2SiO
3Be inorganic dispersant, comprise the following steps:
(1) quantitatively takes by weighing metatitanic acid, add 18% sulphuric acid soln, regulate pH value, stir also and slowly be heated to 90-100 ℃, reacted 1-1.5 hour to 1-2;
(2) quantitatively take by weighing urea, the mol ratio of urea and metatitanic acid is 1: 1-5: 1, add in the solution of step (1), and continued stirring reaction 1-1.5 hour;
(3) quantitatively take by weighing Tai-Ace S 150 or water glass or Tai-Ace S 150+water glass, slowly add in the mixture of step (2), continued stirring reaction 2-3 hour, get white precipitate;
(4) throw out after filtration, after the washing, vacuum-drying 400-800 ℃ of calcining down, obtain the mixture of nano titanium oxide.
Advantage of the present invention is:
1. the present invention adopts even coprecipitation method, and solvent is a water, and product is easy to purifying, and is pollution-free.
2. the present invention adopts precipitin reaction and chemically treated one-step preppn process, and operation is short, and processing condition are controlled, and product structure and particle diameter are controlled.
3. particle diameter of the present invention is little, good dispersity.
Description of drawings
Fig. 1 is the structural representation of mixture for the nuclear shell structured nano-titanium;
Wherein: A-titanium dioxide; The mixture of B-titanium, silicon and/or aluminium.
Fig. 2 is embodiment one, two, three and Comparative Examples experimental result synopsis;
Fig. 3 is an X ray diffracting spectrum;
Fig. 4 is the turbidity-time curve of nano-powder in deionized water.
Embodiment
Embodiment one: the nuclear shell structured nano-titanium is one of preparation method of mixture:
(1) quantitatively takes by weighing metatitanic acid 9.8g, add 18% sulphuric acid soln of 30ml, regulate pH value, stir also and slowly be heated to 95 ℃, reacted 1.5 hours to 1-2;
(2) quantitatively take by weighing urea, the mol ratio of urea and metatitanic acid is 5: 1, adds in the solution of step (1), continues stirring reaction 1.2 hours;
(3) quantitatively take by weighing water glass 3.03g, be dispersed in the 30ml water, slowly add in the mixture of step (2), continued stirring reaction 2.5 hours, get white precipitate;
(4) throw out after filtration, after the washing, vacuum-drying 400 ℃ of calcinings down, obtain the mixture of nanometre titanium dioxide/silicon dioxide.
Embodiment two: the nuclear shell structured nano-titanium be mixture the preparation method two:
(1) quantitatively takes by weighing metatitanic acid 9.8g, add 18% sulphuric acid soln of 30ml, regulate pH value, stir also and slowly be heated to 95 ℃, reacted 1.5 hours to 1-2;
(2) quantitatively take by weighing urea, the mol ratio of urea and metatitanic acid is 5: 1, adds in the solution of step (1), continues stirring reaction 1.2 hours;
(3) quantitatively take by weighing Tai-Ace S 150 2.13g, be dispersed in the 30ml water, slowly add in the mixture of step (2), continued stirring reaction 2.5 hours, get white precipitate;
(4) throw out after filtration, after the washing, vacuum-drying 400 ℃ of calcinings down, obtain the mixture of nano titanium oxide/aluminium sesquioxide.
Embodiment three: the nuclear shell structured nano-titanium be mixture the preparation method three:
(1) quantitatively takes by weighing metatitanic acid 9.8g, add 18% sulphuric acid soln of 30ml, regulate pH value, stir also and slowly be heated to 95 ℃, reacted 1.5 hours to 1-2;
(2) quantitatively take by weighing urea, the mol ratio of urea and metatitanic acid is 5: 1, adds in the solution of step (1), continues stirring reaction 1.2 hours;
(3) quantitatively take by weighing water glass 1.52g and Tai-Ace S 150 1.07g, be dispersed in the 30ml water, slowly add in the mixture of step (2), continued stirring reaction 2.5 hours, get white precipitate;
(4) throw out after filtration, after the washing, vacuum-drying 400 ℃ of calcinings down, obtain the mixture of nanometre titanium dioxide/silicon dioxide/aluminium sesquioxide.
Comparative Examples: Preparation by Uniform Precipitation nano titanium oxide
(1) quantitatively takes by weighing metatitanic acid 9.8g, add 18% sulphuric acid soln of 30ml, regulate pH value to 1~2, stir also and slowly be heated to 95 ℃, reaction 1.5hr;
(2) quantitatively take by weighing urea, the mol ratio of urea and metatitanic acid is 5: 1, adds in the solution of step (1), continues stirring reaction 1.2hr;
(3) throw out after filtration, after the washing, vacuum-drying 400 ℃ of calcinings down, obtain nano titanium oxide.
Nano titanium oxide through the above-mentioned steps preparation is a mixture, detect through transmission electron microscope, primary particle is of a size of 30-80nm, detect through X-ray diffraction, grain-size is 10-30nm, through X-ray electron spectroscopy analysis, the oxide compound of silicon or aluminium mainly is enriched in the shell on surface, through the settleability analysis, this nuclear shell structured nano-titanium is that the settling velocity of mixture in deionized water is slow, the dispersed nano titanium oxide that is better than greatly with the quadrat method preparation.
Claims (4)
1. a nuclear shell structured nano-titanium is a mixture, and its component is:
TiO
2:90-99%
SiO
2Or Al
2O
3Or SiO
2+ Al
2O
3: 1-10%.
2. nuclear shell structured nano-titanium according to claim 1 is a mixture, it is characterized in that: the particle diameter of described mixture is 30-80nm.
3. preparation method that aforesaid nuclear shell structured nano-titanium is a mixture, it is characterized in that: adopting even coprecipitation method, is raw material with the metatitanic acid, and urea is precipitation agent, with Al
2(SO
4)
3Or Na
2SiO
3Or Al
2(SO
4)
3+ Na
2SiO
3Be inorganic dispersant.
4. nuclear shell structured nano-titanium according to claim 3 is the preparation method of mixture, it is characterized in that comprising the following steps:
(1) quantitatively takes by weighing metatitanic acid, add 18% sulphuric acid soln, regulate pH value, stir also and slowly be heated to 90-100 ℃, reacted 1-1.5 hour to 1-2;
(2) quantitatively take by weighing urea, the mol ratio of urea and metatitanic acid is 1: 1-5: 1, add in the solution of step (1), and continued stirring reaction 1-1.5 hour;
(3) quantitatively take by weighing Tai-Ace S 150 or water glass or Tai-Ace S 150+water glass, slowly add in the mixture of step (2), continued stirring reaction 2-3 hour, get white precipitate;
(4) throw out after filtration, after the washing, vacuum-drying 400-800 ℃ of calcining down, obtain the mixture of nano titanium oxide.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB031322174A CN1194935C (en) | 2003-07-31 | 2003-07-31 | Core-shell structure nano titanium serial composition and its preparing method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CNB031322174A CN1194935C (en) | 2003-07-31 | 2003-07-31 | Core-shell structure nano titanium serial composition and its preparing method |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1473791A true CN1473791A (en) | 2004-02-11 |
CN1194935C CN1194935C (en) | 2005-03-30 |
Family
ID=34154046
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB031322174A Expired - Fee Related CN1194935C (en) | 2003-07-31 | 2003-07-31 | Core-shell structure nano titanium serial composition and its preparing method |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1194935C (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1328217C (en) * | 2004-10-21 | 2007-07-25 | 华楙生化科技股份有限公司 | Core-shell structured powder production method |
CN100503448C (en) * | 2006-05-23 | 2009-06-24 | 中国科学院理化技术研究所 | Method for synthesizing anatase type crystallized titanium dioxide nano core-shell or hollow-shell structure material by aqueous phase one-step |
CN105873677A (en) * | 2014-01-28 | 2016-08-17 | 夏普株式会社 | Photocatalyst material and method for producing same |
-
2003
- 2003-07-31 CN CNB031322174A patent/CN1194935C/en not_active Expired - Fee Related
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1328217C (en) * | 2004-10-21 | 2007-07-25 | 华楙生化科技股份有限公司 | Core-shell structured powder production method |
CN100503448C (en) * | 2006-05-23 | 2009-06-24 | 中国科学院理化技术研究所 | Method for synthesizing anatase type crystallized titanium dioxide nano core-shell or hollow-shell structure material by aqueous phase one-step |
CN105873677A (en) * | 2014-01-28 | 2016-08-17 | 夏普株式会社 | Photocatalyst material and method for producing same |
Also Published As
Publication number | Publication date |
---|---|
CN1194935C (en) | 2005-03-30 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1128106C (en) | Method for prodn. of mono-dispersed and crystalline TiO2 ultrafine powders from aqueous TiOCl2 solution using homogeneous precipitation | |
CN1263807C (en) | Methods for producing titanium dioxide having improved gloss at low temp. | |
WO2011086567A1 (en) | Magnetic dye-adsorbent catalyst | |
CN1884095A (en) | UV-shielding nano normal zinc titanate powder and process for preparing same | |
CN101058679A (en) | Method of preparing sericite ultraviolet radiation screening agent | |
CN101049563A (en) | Preparing Nano Ag/CeO2 catalyst possessing catalytic activity of visible light | |
CN114773882B (en) | Titanium dioxide for delustering chinlon chemical fiber and preparation method thereof | |
CN1927452A (en) | Ternary composite octahedrite type titanium dioxide photocatalyst and preparation process thereof | |
Watson et al. | Studies on the preparation of magnetic photocatalysts | |
CN1398789A (en) | Prepn of nano barium sulfate | |
CN111715188A (en) | Titanium dioxide-based nano composite material and preparation method and application thereof | |
Zeng et al. | Comparison of the phase transition and degradation of methylene blue of TiO2, TiO2/montmorillonite mixture and TiO2/montmorillonite composite | |
Zhang et al. | Effect of calcination temperature on the structure and properties of SiO2 microspheres/nano-TiO2 composites | |
JP4681879B2 (en) | Producing a solution for use as a coating in a transparent film of a photocatalyst | |
CN1709567A (en) | Hydrothermal method for preparing nano crystal Bi2WO6 powder photocatalytic material with visible light activity | |
Zhang et al. | Immobilization of penicillin G acylase on a novel paramagnetic composite carrier with epoxy groups | |
CN110694607A (en) | Preparation method and application of activated carbon silicon dioxide/zinc oxide composite photocatalyst | |
CN1194935C (en) | Core-shell structure nano titanium serial composition and its preparing method | |
CN1778682A (en) | Production of nanometer copper oxide with controllable microstructure | |
CN1171796C (en) | Oxidation and coprecipitation process of preparing Sb-doped nano tin dioxide | |
Khaksar et al. | In situ solvothermal crystallization of TiO 2 nanostructure on alumina granules for photocatalytic wastewater treatment | |
CN1891335A (en) | Method for preparing nano titanium dioxide photocatalyst and its product | |
CN112246264B (en) | Molybdenum carbide metal molybdenum silicon carbide ternary composite material, preparation method thereof and effect of molybdenum carbide metal molybdenum silicon carbide ternary composite material on photocatalytic hydrogen production | |
CN1268548C (en) | Method for preparing rutile titanic oxide electronic powder with metatitanic acid as main material | |
CN1530327A (en) | Preparing method for crystalline nanometer titania material with controllable size |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
C19 | Lapse of patent right due to non-payment of the annual fee | ||
CF01 | Termination of patent right due to non-payment of annual fee |