CN1375449A - Perovskite type La1-x-yBaxDyyMnO3 compound oxide superfine particle and its prepn. - Google Patents
Perovskite type La1-x-yBaxDyyMnO3 compound oxide superfine particle and its prepn. Download PDFInfo
- Publication number
- CN1375449A CN1375449A CN 01109482 CN01109482A CN1375449A CN 1375449 A CN1375449 A CN 1375449A CN 01109482 CN01109482 CN 01109482 CN 01109482 A CN01109482 A CN 01109482A CN 1375449 A CN1375449 A CN 1375449A
- Authority
- CN
- China
- Prior art keywords
- mno
- solution
- ultrafine particle
- perovskite
- composite oxides
- 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
- Catalysts (AREA)
Abstract
The present invention uses nitrate containing La, Ba, Dy and Mn as raw material, dissolves it in water to obtain solution (A) and dissolves Na2CO3 and NaOH in water to obtain solution (B), mixes two solutions and makes them undergo the processes of stirring, precipitation and washing, drying precipitate and roasting it to obtain the invented La1-x-yBaxDyyMnO3 perovskite type rare earth compound oxide superfine particles. Their mean grain size is 10-50 nm, and specific area is 15-50 sq.m g(-1), and the grain size distribution is narrow, so that it possesses high catalytic activity for complete oxidation of CO, CH4 and volatile organic substance.
Description
The present invention relates to a kind of complex rare-earth oxidate containing valuable metal ultrafine particle and preparation method thereof, it is raw material with nitrate, makes through processes such as precipitation, drying, roastings.
La
1-x-yBa
xDy
yMnO
3Belong to perovskite composite oxide, it can be used for combustioncatalysts, cleaning catalyst for tail gases of automobiles and new ceramic material etc.It is that specific surface area is too little as one of existing key issue of catalyzer, so the technology of preparing of bigger serface perovskite-type rare-earth composite oxides is quite with practical value.Its preparation can be adopted atomizing freeze drying method or organic reagent complexometry etc.With the atomizing freeze drying method [Catal, Letters, 1993,21: //; Appl, Catal.A, 1994,109:181] specific surface area of the perovskite-type rare-earth composite oxides that makes can reach 22.7m
2g
-1, but specific surface area is just reduced to 11.7m after 800 ℃ of roastings
2g
-1And this method needs liquid nitrogen refrigerating, production cost height.Adopt the organic reagent complexometry can make the higher perovskite-type rare-earth composite oxides of specific surface area [Appl, Catal., 1986,26:265; Stud.in suf.Sci.and Catal., 1998,118:431], yet this method is raw material with the organic reagent, the cost height.By organic acid salt, decomposition can make perovskite-type rare-earth composite oxides ultrafine particle [JP4193701A2] as acetate, and the particle diameter of its product reaches one micron, and the cost of organic acid salt is than higher.Patent [US5939354, US5977017] is a raw material with inorganic salt or oxide compound, and hydroxy-butanedioic acid is a precipitation agent, and the specific surface area that makes perovskite-type rare-earth composite oxides is up to 30m
2g
-1Weak point is, hydroxy-butanedioic acid price height, and the carbon in the two hydroxy-butanedioic acid has disadvantageous effect to the catalytic performance of product.
The purpose of this invention is to provide a kind of perovskite typed La
1-x-yBa
xDy
yMnO
3Composite oxides ultrafine particle and preparation method thereof, this method are raw material with the rare earth nitrate, to contain Na
+And CO
3 2-The ionic mixed alkali liquor is a precipitation agent, makes the ultrafine particle that specific surface area is big, particle diameter is little through chemical reaction, drying, roasting.
The objective of the invention is to realize by following measure:
Perovskite typed La
1-x-yBa
xDy
yMnO
3X in the chemical constitution formula of composite oxides ultrafine particle is between 0.1～0.3, and y is between 0.05～0.15, and median size is 10～50nm, and specific surface area is 15～50m
2g
-1, bulk structure is single perovskite structure.
It is raw material with nitrate, makes through processes such as precipitation, drying, roastings, it is characterized in that by forming expression La
1-x-yBa
xDy
yMnO
3The nitrate that contains La, Ba, Dy, Mn of getting stoichiometric ratio is water-soluble, makes solution (I), gets Na
2CO
3With water-soluble solution (II), the wherein Na of making of NaOH
2CO
3And the mol ratio of NaOH is between 0.2 to 2.0, solution (I) and solution (II) are mixed, carry out chemical reaction, the pH value of control reaction is between 4～12, this process forms flocks, again through stirring 1～5 hour after-filtration, washing, will be deposited in air at room temperature to 120 ℃ temperature range drying 8～24 hours after the washing, 300 ℃～500 ℃ temperature range preroastings 1 hour～3 hours, the temperature roasting just got perovskite typed La in 2～4 hours between 600 ℃～1200 ℃ then
1-x-yBa
xDy
yMnO
3The composite oxides ultrafine particle.
The advantage of present method is: a process for preparing the La of single perovskite structure
1-x-yBa
xDy
yMnO
3Ultrafine particle detects less than other compound with X-ray diffraction means, and is different with proportioning according to maturing temperature, the particle median size between 10～50nm, the particle size distribution narrow range.Specific surface area is at 15m
2G-50m
2g
-1Between, it is to CO, CH
4Present high catalytic activity with the complete oxidation of volatile organic matter.
The synthetic hot stage that carries out solid state reaction of experience that needs of perovskite-type rare-earth composite oxides will be so the homodisperse of each component will be beneficial to the carrying out of solid state reaction in the presoma.Present method is precipitation agent with carbonate and controls pH value between 4～12, is intended to form the purpose of double salt with the homodisperse that reaches each component molecular level.Ultra-fine grain is easy to assemble and longly is macrobead, particularly more than 700 ℃ during high temperature; The agglomeration of particles growth process is achieved by the intergranular surface diffusion migration that contacts.Present method has specific structure at perovskite-type rare-earth composite oxides, and the size of the metal ion that constitutes it and valence state etc. is had the characteristics of certain requirement; In the preparation process, Ba mixes in presoma
2+And Dy
3+Ion, this dopant ion are enriched in the surface and form the substitution ion of calcium titanium type complex rare-earth oxidate containing valuable metal after high-temperature roasting; This unique texture that forms on the surface has played the effect that particle aggregation is grown up that hinders.These 2 is the characteristics place of the present invention on thinking.Among this preparation method, lanthanum, manganese, barium, the isoionic basic carbonate double salt precipitation of dysprosium have been generated, owing to these ions are present in the macromole, so each component has obtained the homodisperse of molecular level through acid-base reaction.
Present method has been removed water and planar water and the part-structure water that precipitates in the hole by drying, and the purpose of preroasting is to decompose the nitrate radical plasma that removal retains.The temperature roasting then is the forming process of perovskite structure and the surface enrichment process of dopant ion more than 600 ℃.
Granular size records with transmission electron microscope in the following example, and specific surface area is recorded by the liquid nitrogen physical adsorption on ASAP2000 type physical adsorption appearance.
Description of drawings: this accompanying drawing is preparation method's process flow sheet.
Example is to produce 100 gram La
0.7Dy
0.1Ba
0.2MnO
3Ultrafine particle is a benchmark, and (1) gets 124 gram La (NO
3)
36H
2O, 21 gram Ba (NO
3)
2, 14 gram Dy (NO
3)
3, the Mn (NO of 147 grams 50%
3)
2Solution and 1080ml deionized water are made solution (I).Get 108 gram Na
2CO
3, 42 gram NaOH and 720ml deionized waters make solution (II).In the deionized water with solution (I) and solution (II) and stream adding 320ml, keep PH in 10 ± 0.5 scopes.And stream generates the khaki color precipitation after finishing.Stirring at room 120 minutes, precipitation darkened in the whipping process.(2) filter, with deionized water wash to Na
+Content in precipitation is less than 10ppm.To be deposited in making beating-filtration in the dehydrated alcohol then, so triplicate.(3) filter cake is in 80 ℃ of still airs dry 20 hours, 350 ℃ of roastings 2 hours, 800 ℃ of roastings 2 hours product.
Product is single perovskite structure La
0.7Dy
0.1Ba
0.2MnO
3Composite oxides ultrafine particle, its median size are 12nm, and specific surface area is 38.6m2g-1, is catalyzer with this ultrafine particle, on fixed-bed reactor, at air speed 20000mlg
-1h
-1, temperature is 390 ℃, 3.5%CH
4, 18%O
2, 78.5%N
2In the atmosphere, 99% above CH
4Be oxidized to CO
2And water.
Claims (2)
1. perovskite typed La
1-x-yBa
xDy
yMnO
3The composite oxides ultrafine particle is characterized in that x in the chemical constitution formula of ultrafine particle between 0.1～0.3, and y is between 0.05～0.15, and median size is 10～50nm, and specific surface area is 15～50m
2g
-1, bulk structure is single perovskite structure.
2. perovskite typed La
1-x-yBa
xDy
yMnO
3The preparation method of composite oxides ultrafine particle, it is raw material with nitrate, makes through processes such as precipitation, drying, roastings, it is characterized in that by forming expression La
1-x-yBa
xDy
yMnO
3The nitrate that contains La, Ba, Dy, Mn of getting stoichiometric ratio is water-soluble, makes solution (I), gets Na
2CO
3With water-soluble solution (II), the wherein Na of making of NaOH
2CO
3And the mol ratio of NaOH is between 0.2 to 2.0, solution (I) and solution (II) are mixed, carry out chemical reaction, the pH value of control reaction is between 4～12, this process forms flocks, again through stirring 1～5 hour after-filtration, washing, will be deposited in air at room temperature to 120 ℃ temperature range drying 8～24 hours after the washing, 300 ℃～500 ℃ temperature range preroastings 1 hour～3 hours, the temperature roasting just got perovskite typed La in 2～4 hours between 600 ℃～1200 ℃ then
1-x-yBa
xDy
yMnO
3The composite oxides ultrafine particle.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB011094826A CN1170763C (en) | 2001-03-15 | 2001-03-15 | Perovskite type La1-x-yBaxDyyMnO3 compound oxide superfine particle and its prepn. |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB011094826A CN1170763C (en) | 2001-03-15 | 2001-03-15 | Perovskite type La1-x-yBaxDyyMnO3 compound oxide superfine particle and its prepn. |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1375449A true CN1375449A (en) | 2002-10-23 |
| CN1170763C CN1170763C (en) | 2004-10-13 |
Family
ID=4657956
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB011094826A Expired - Fee Related CN1170763C (en) | 2001-03-15 | 2001-03-15 | Perovskite type La1-x-yBaxDyyMnO3 compound oxide superfine particle and its prepn. |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN1170763C (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100349654C (en) * | 2004-09-03 | 2007-11-21 | 石油大学(北京) | Nano superfine micro-particle catalyst for carbon particle combustion in diesel engine tail gas and preparing method therefor |
| CN101284215B (en) * | 2008-06-03 | 2011-06-15 | 华南理工大学 | Preparation method of perovskite hollow fiber membrane |
| CN102603299A (en) * | 2012-03-22 | 2012-07-25 | 中北大学 | High conductivity nanometer complex phase perovskite type proton conductor |
| CN102765964A (en) * | 2012-06-29 | 2012-11-07 | 南京工业大学 | Method for improving specific surface area of perovskite oxide through liquid post-treatment |
| CN103449536A (en) * | 2013-08-30 | 2013-12-18 | 华北水利水电大学 | Preparation method of perovskite type nano Nd1-xMgxCoO3 |
| CN112125281A (en) * | 2020-10-28 | 2020-12-25 | 中国科学院上海应用物理研究所 | Method for preparing lanthanide oxide material by using coprecipitation combined with molten salt deposition method and application thereof |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100431693C (en) * | 2006-11-10 | 2008-11-12 | 北京工业大学 | Process for preparing catalyst contg. La(1-x)SrxMO3 used for removing volatile organic matter |
-
2001
- 2001-03-15 CN CNB011094826A patent/CN1170763C/en not_active Expired - Fee Related
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN100349654C (en) * | 2004-09-03 | 2007-11-21 | 石油大学(北京) | Nano superfine micro-particle catalyst for carbon particle combustion in diesel engine tail gas and preparing method therefor |
| CN101284215B (en) * | 2008-06-03 | 2011-06-15 | 华南理工大学 | Preparation method of perovskite hollow fiber membrane |
| CN102603299A (en) * | 2012-03-22 | 2012-07-25 | 中北大学 | High conductivity nanometer complex phase perovskite type proton conductor |
| CN102765964A (en) * | 2012-06-29 | 2012-11-07 | 南京工业大学 | Method for improving specific surface area of perovskite oxide through liquid post-treatment |
| CN102765964B (en) * | 2012-06-29 | 2014-04-09 | 南京工业大学 | Method for improving specific surface area of perovskite oxide through liquid post-treatment |
| CN103449536A (en) * | 2013-08-30 | 2013-12-18 | 华北水利水电大学 | Preparation method of perovskite type nano Nd1-xMgxCoO3 |
| CN112125281A (en) * | 2020-10-28 | 2020-12-25 | 中国科学院上海应用物理研究所 | Method for preparing lanthanide oxide material by using coprecipitation combined with molten salt deposition method and application thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1170763C (en) | 2004-10-13 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Hou et al. | Recent advances in cobalt-activated sulfate radical-based advanced oxidation processes for water remediation: A review | |
| AU2020377609B2 (en) | Hydrogenated TiO2 denitration catalyst, preparation method therefor and application thereof | |
| CN111359625B (en) | Carbon composite nano cobaltosic oxide-based formaldehyde normal-temperature catalyst and preparation method thereof | |
| KR100655133B1 (en) | METAL OXIDE CATALYST FOR REMOVING NOx AND METHOD OF PREPARING THE SAME | |
| CN1170763C (en) | Perovskite type La1-x-yBaxDyyMnO3 compound oxide superfine particle and its prepn. | |
| CN109772465A (en) | A kind of preparation method of water solubility carbon dots modified perovskite type catalysis material | |
| CN111167432A (en) | Cerium oxide-hydrotalcite composite catalyst, preparation method and application | |
| CN106799249B (en) | For N2Co oxide/BaCO of O catalytic decomposition3Catalyst and preparation method thereof | |
| CN115676896A (en) | Amorphous manganese oxide composite material and preparation method and application thereof | |
| CN110743537A (en) | OMS-2 catalytic material and preparation method and application thereof | |
| CN110560062A (en) | Preparation method and application of two-dimensional iron oxide nanosheet catalyst | |
| EP1478459A1 (en) | Metal-oxide supported au catalysts, method for their production and use thereof | |
| CN103212419B (en) | Preparation method and application of catalyst for treating acrylonitrile contained waste gas | |
| CN115138367A (en) | Ozone oxidation catalyst and preparation method and application thereof | |
| US6911413B2 (en) | Nano-gold catalyst and process for preparing the same | |
| CN101759232A (en) | Porous manganese dioxide of nanofibre texture and preparation method thereof | |
| US11554362B2 (en) | Rare-earth metal vanadates catalysts for NOx reduction at low temperatures | |
| CN104624203B (en) | Pb modified Co oxide matrix N2O decomposition catalyst as well as preparation method and application of catalyst | |
| CN114471531A (en) | Nano porous spherical birnessite, preparation method thereof and application thereof in formaldehyde degradation | |
| Zhang et al. | Research progress on the preparation of alkali/alkaline earth metal-modified metal oxide catalysts and their application to diesel engine exhaust soot particle catalytic purification | |
| CN114149068B (en) | High-valence iron-containing Fe (IV) perovskite type composite oxide and low-temperature roasting synthesis method and application thereof | |
| JPH08183617A (en) | Production of fine lepidocrocite particles or powder | |
| KR101891110B1 (en) | Reinforced extinguishing agent for removal of carbon monooxide and producing method thereof | |
| CN115501877A (en) | Layered composite cobalt cerium catalyst for catalyzing selective oxidation of ammonia nitrogen in water by ozone and preparation method and application thereof | |
| CN114749163A (en) | Preparation method of Ce-Al dephosphorization material |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| C10 | Entry into substantive examination | ||
| SE01 | Entry into force of request for substantive examination | ||
| 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 |