CN1760157A - A kind of preparation method of lutecia based transparent ceramics - Google Patents
A kind of preparation method of lutecia based transparent ceramics Download PDFInfo
- Publication number
- CN1760157A CN1760157A CN 200510027208 CN200510027208A CN1760157A CN 1760157 A CN1760157 A CN 1760157A CN 200510027208 CN200510027208 CN 200510027208 CN 200510027208 A CN200510027208 A CN 200510027208A CN 1760157 A CN1760157 A CN 1760157A
- Authority
- CN
- China
- Prior art keywords
- preparation
- based transparent
- transparent ceramics
- lutecia
- sintering
- 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
- Compositions Of Oxide Ceramics (AREA)
- Luminescent Compositions (AREA)
Abstract
The present invention relates to a kind of preparation method of lutecia based transparent ceramics, belong to the transparent optical ceramic field.The present invention adopts ammoniacal liquor to add bicarbonate of ammonia and is used as compound precipitants and lutetium and dopant ion nitrate by proportioning (Lu
1-xRE
x)
2O
3Form the precipitation presoma, RE is the Doped Rare Earth ion in the formula, x represents the molar weight of dopant ion, 0≤x≤0.30 is through ageing, washing, drying, calcining, moulding and can obtain the lutecia based base ceramic material of the highly transparent of visible waveband straight line transmitance more than 80% by pressureless sintering in the mobile nitrogen atmosphere.
Description
Technical field
The present invention relates to a kind of preparation method of lutecia based transparent ceramics, more precisely relate to, belong to the transparent optical ceramic field with wet-chemical lutecia based powder of coprecipitation method synthesis of nano and atmosphere pressureless sintering method thereof.
Background technology
Along with the fast development of photoelectron and information detection technology, need a large amount of high performance optical functional materialses crucial basic substance is provided.Because advanced inorganic materials preparation method's continuous progress and innovation, transparent ceramic material more and more shows its unique advantage, and growth momentum is very swift and violent.Crystalline ceramics has characteristics such as high temperature resistant, corrosion-resistant, the high insulation of ceramic inherent, high strength, has the optical property of glass again, and large-sized monocrystalline material growth needs the equipment and the complicated technology of special expensive, and the production cycle is long, cost height, scrap rate height.Special in the novel optical function material with complicated dopant states, traditional crystal technique is difficult to guarantee the high density and the uniform distribution of dopant ion, and then can't realize the optical property optimization of material.The continuous progress of crystalline ceramics technology of preparing makes development polycrystalline ceramics scintillator and ceramic laser material become possibility.Crystalline ceramics preparation technology is simple, and cost is lower, can be significantly less than the preparation of finishing the high-compactness optical material under the temperature of material melting point, and the technology required time is far below the pulling crystal required time.Be easy to realize the mass low cost production.Particularly can require to realize the even doping of high concentration ion according to device application more conveniently, avoid because crystal growth technique limits low, the pockety situation of doping content that is caused, and this raising to the material luminescent properties be most important.The performance of crystalline ceramics has has met or exceeded monocrystal material under a stable condition, is expected in some specific occasions progressively substitute the monocrystalline optical material.
Since first transparent Al
2O
3Since pottery " Lucalox " came out, crystalline ceramics had been developed Al in succession through the development of decades
2O
3, Y
2O
3, MgO, ZrO
2Deng oxidic transparent pottery and AlN, CaF
2Etc. Non-oxide Transparent Ceramics.Crystalline ceramics is applied to aspects such as lighting and saturating ripple window at first, and last decade comes, GE, and Siemens, company such as Hitachi and some research units have carried out the research of ceramic scintillator in succession, develop (Y, Gd)
2O
3: Eu, Pr (YGO), Gd
2O
2S:Pr, Ce, F (GOS), Gd
3Ga
5O
12: Cr, Ce rare earth oxide ceramic scintillators such as (GGG), and successfully they are applied on the medical science X-CT.In addition, the someone attempted crystalline ceramics is applied to optoelectronic areas again in recent years, as with YAG, and Y
2O
3Developed Nd as matrix
3+: YAG, Nd
3+: Y
2O
3Deng the ceramic laser material.
And Y
2O
3Lutecium oxide (Lu with same crystal structure
2O
3) have a high density (～9.42g/cm
3), Lu Atom of Elements (71) is also higher simultaneously, and this makes it quite high to the stopping power of all kinds of rays (X ray, gamma-rays), Lu
2O
3Band gap very wide (6.5ev) can hold many activator ions such as Eu as the luminescent material matrix between valence band and conduction band, Tb, Tm, the emission level of Er etc.Lutecium oxide Lu
2O
3Have extremely good physical and chemical stability, be not subjected to the influence of other component of atmosphere.As the Lu of the 5%Eu that mixes
2O
3The light output of base transparent flickering body is approximately 50%CsI:Tl, is applicable to the X ray digital imagery.In addition, Lu
2O
3Body material has high heat conductance, low thermal coefficient of expansion, low effective phonon energy, can make solid statelaser superpower ceramic laser material by mixing Nd or Yb.
In sum, Lu
2O
3Be a kind of extremely promising luminescent material matrix.Yet Lu
2O
3Fusing point is up to 245O ℃, and the employing Czochralski grown contains the not only difficult realization of technology of monocrystal material of various doping components, and cost is quite high.Lu
2O
3Have cubic crystal structure, optical isotropy, specific refractory power does not rely on directivity, can powder be made crystalline ceramics by nanocrystalline technology and reducing atmosphere pressureless sintering technology.Therefore developing the lutecia based transparent ceramics material is that this class material obtains key in application.And the key that obtains transparent ceramic material is the precursor powder for preparing the sintering character excellence earlier, requires powder to have good dispersiveness, little particle size, and spheroidal particle pattern, wet chemistry method are the most feasible methods that reaches this purpose.
Existing in the world several families begin Lu
2O
3The research of base transparent ceramic.For example, the synthetic Eu of human oxalate precipitation method such as A.Lempicki
3+Adulterated Lu
2O
3Ceramic scintillator is because oxalate K
SpBigger, it is bigger to adopt the oxalate precipitation method to obtain the powder granule size, and very easily reunites.E.Zych etc. utilize urea to make fuel with the synthetic RE of solution combustion method
3+Adulterated Lu
2O
3Luminescent powder, vacuum sintering then only can obtain translucent ceramics sample, and this is that sintering activity is low because the burning synthetic powder is reunited seriously.J.Lu adopts the urea precipitation from homogeneous solution (PFHS) to prepare powder, and vacuum sintering prepares Lu then
2O
3: Nd
3+The ceramic laser material, however hydrolysis of urea speed is slower, and productive rate is lower, and particle is relatively large.The pressureless sintering technology prepares crystalline ceramics requirement powder and has good dispersiveness and high sintering activity.Coprecipitation method is widely used for synthetic various oxide ceramic powder bodies as a kind of typical powder preparing technology, is to be fit to be used for preparing a kind of wet chemistry method of crystalline ceramics with powder.
Summary of the invention
The present invention adopts the mixed solution of ammoniacal liquor and ammonium hydrogencarbonate as compound precipitants, and the mol ratio of control ammoniacal liquor and bicarbonate of ammonia prepares the active Lu of high sintering by coprecipitation technology
2O
3Powder, and be placed in the reducing atmosphere stove, prepare the rear-earth-doped oxidation lutetium base optical ceramics of highly transparent with normal atmosphere sintering method.
The object of the present invention is to provide and a kind ofly prepare rare earth ion doped Lu with coprecipitation method
2O
3Base nano-powder, and the method for nitrogen atmosphere pressureless sintering crystalline ceramics.
The RE of the present invention's preparation
3+Doping Lu
2O
3Transparent ceramic material, its general formula is expressed as: (Lu
1-xRE
x)
2O
3, RE is the Doped Rare Earth ion in the formula, as Eu, and Tb, Nd, Yb, one or both among the Tm, x are represented the molar weight of dopant ion, common 0≤x≤0.30; Preparation process comprises the steps:
(1) powder preparing: synthetic powder of the present invention is for being to add bicarbonate of ammonia as compound precipitants by employing ammoniacal liquor, and the mol ratio of control ammoniacal liquor and bicarbonate of ammonia is 0.01-3; Press the composition formula proportioning and introduce lutetium ion and amounts of dopant ions, and compound precipitants forms the precipitation presoma and control final pH value and be controlled between the 8-9, after the drying, in 800-1200 ℃ of calcining 1-5 hour with the form of nitrate.The diameter of particle that obtains is 20-50nm, and narrow diameter distribution, do not have reunion substantially, particle is intimate spherical in shape.
(2) moulding: the two-way compacting of punching block is adopted in the powder moulding, and is dry-pressing formed in 10-50MPa, and the back is in the 100-300MPa isostatic pressing.
(3) sintering: the pressureless sintering in the mobile nitrogen atmosphere of the biscuit after the moulding, soaking time 3-9 hour, can obtain the lutecia based transparent ceramics of highly transparent by sintering temperature 1750-1950 ℃.
RE is synthesized in co-precipitation provided by the invention
3+Doping Lu
2O
3The characteristics of the preparation of nano-powder and the non-pressure sintering technology of crystalline ceramics are:
(1) can mix other rare earth ion as required easily, and can reach the evenly mixed of atom level in solution, Lu is advanced in solid solution
2O
3The matrix lattice.
The powder of characteristics such as (2) existence of an amount of carbanion can obtain to have low reunion, narrow particle size distribution, pattern are close to spherical in shape, sintering activity height.
(3) normal pressure nitrogen atmosphere sintering can obtain the transparent ceramics sample of high compaction.The Archimedes method is measured its density near theoretical density, the about 50-60 μ of grain size m, and visible waveband straight line transmitance reaches more than 80%
(4) according to the difference of mixing activator ion, can realize flicker, different optical such as last conversion and laser are used.
Description of drawings
Fig. 1 obtains the TEM photo of precipitation presoma by compound precipitants.The sedimentary dispersiveness of presoma is better.
Fig. 2 obtains Lu for precipitating after presoma is calcined 2h through 1000 ℃
2O
3The XRD figure spectrum of powder shows that product is a single cube of phase.
Fig. 3 obtained the TEM of powder in 2 hours in 850 ℃ of calcinings for the precipitation presoma.Particles dispersed is good, is close to globulate, the about 20nm of average grain size.
Fig. 4 is the TEM pattern of precipitation presoma in 2 hours powders of 1000 ℃ of calcinings.Particles dispersed is good, the about 30nm of average grain size.
Fig. 5 is the photo (1mm is thick) of sample after the surface finish.Sample has the good optical transparency.
Fig. 6 for sample after the surface finish in the transmittance curve of visible waveband.Transmitance at visible waveband surpasses 80%.
The fresh fracture apperance of Fig. 7 sintering transparent ceramics.About average grain size 50 μ m, do not observe the existence of defectives such as pore, have the micro-structural feature of typical crystalline ceramics.
Embodiment
Further illustrate the present invention with the form of embodiment below but not limitation embodiment.
Embodiment 1
Get 5ml ammoniacal liquor, the ammonium bicarbonate soln uniform mixing of 250ml1mol/l is titrated to the Lu (NO that fills 75.7ml 0.815mol/l in the pyriform funnel of 500ml
3)
3Eu (NO with 4ml 0.812mol/l
3)
3The beaker of mixing solutions in, the while vigorous stirring, the about 5ml/min of rate of titration, the pH value of titration end point is controlled to be between the 8-9, and titration finishes to continue to stir 30min, will precipitate presoma in room temperature ageing 2 days, ageing finishes and uses deionized water wash 4 times, the vacuum pump suction filtration, the dehydrated alcohol rinsing is 2 times then, the precipitation presoma after the filtering and washing is placed 80 ℃ the dry 24h of baking oven.Calcine 2h at 850 ℃ and 1000 ℃ respectively afterwards in retort furnace, furnace cooling promptly gets required nano-powder.Dry-pressing is adopted in the powder moulding, waits static pressure then.Dry-pressing is the biscuit with the two-way Φ of the being pressed into 20mm of punching block, forming pressure 30MPa, and waiting static pressure is to adopt oil bath, forming pressure 200MPa.At last, the biscuit after the moulding places hydrogen furnace by the reducing atmosphere non-pressure sintering technology, in 1850 ℃ temperature insulation 6h, can obtain the 5%Eu of highly transparent
3+Doping Lu
2O
3Base transparent optical pottery.
Embodiment 2
Get 15ml ammoniacal liquor, the ammonium bicarbonate soln uniform mixing of 500ml 1mol/l is titrated to the Lu (NO that fills 52.6ml 0.815mol/l in the funnel of 500ml
3)
3Tb (NO with 0.5ml 0.866mol/l
3)
3The beaker of 3000ml of mixing solutions in, remaining step is with embodiment 1.Can obtain the adulterated Lu of 1%Tb
2O
3Crystalline ceramics.
Get 15ml ammoniacal liquor, the ammonium bicarbonate soln uniform mixing of 250ml1mol/l is titrated to the Lu (NO that fills 59.83ml 0.815mol/l in the funnel of 500ml
3)
3Nd (NO with 5ml 0.0985mol/l
3)
3The beaker of 3000ml of mixing solutions in, remaining step is with embodiment 1.Can obtain the adulterated Lu of 1%Nd
2O
3Crystalline ceramics.
Embodiment 4
Get 15ml ammoniacal liquor, the ammonium bicarbonate soln uniform mixing of 250ml 1mol/l is titrated to the Lu (NO that fills 37.3ml 0.815mol/l in the funnel of 500ml
3)
3Yb (NO with 20ml 0.08mol/l
3)
3The beaker of 3000ml of mixing solutions in, remaining step is with embodiment 1.Can obtain the adulterated Lu of 1%Yb
2O
3Crystalline ceramics.
Embodiment 5
Get 7.5ml ammoniacal liquor, the ammonium bicarbonate soln uniform mixing of 475ml 1mol/l is titrated to the Lu (NO that fills 72.88ml 0.815mol/l in the funnel of 500ml
3)
3Tm (NO with 10ml 0.06mol/l
3)
3The beaker of 3000ml of mixing solutions in, remaining step is with embodiment 1.Can obtain the adulterated Lu of 1%Tm
2O
3Crystalline ceramics.
Claims (6)
1, a kind of preparation method of lutecia based transparent ceramics is characterized in that:
(1) presses composition formula (Lu
1-xRE
x)
2O
3With the form proportioning lutetium ion and the amounts of dopant ions of nitrate, RE is the Doped Rare Earth ion in the formula, and x represents the molar weight of dopant ion, 0≤x≤0.30;
(2) adopt ammoniacal liquor to add bicarbonate of ammonia as compound precipitants;
(3) nitrate and compound precipitants mixing gained precipitation agent presoma are obtained lutecia based transparent ceramics behind ageing, washing, drying, calcining, moulding, sintering.
2, by the preparation method of the described a kind of lutecia based transparent ceramics of claim 1, it is characterized in that described dopant ion is Eu, Tb, Nd, Yb, one or both among the Tm.
3, by the preparation method of the described a kind of lutecia based transparent ceramics of claim 1, the mol ratio that it is characterized in that described ammoniacal liquor and bicarbonate of ammonia is 0.01-3.
4,, it is characterized in that calcination condition is 800-1200 ℃ of calcining 1-5 hour by the preparation method of claim 1 or 2 or 3 described a kind of lutecia based transparent ceramics.
5, by the preparation method of claim 1 or 2 or 3 described a kind of lutecia based transparent ceramics, it is characterized in that described condition of molding for adopting the two-way compacting of punching block, dry-pressing formed in 10-50MPa, the back is in the 100-300MPa isostatic pressing.
6, by the preparation method of claim 1 or 2 or 3 described a kind of lutecia based transparent ceramics, it is characterized in that described sintering condition is pressureless sintering in the mobile nitrogen atmosphere, sintering temperature 1750-1950 ℃, soaking time 3-9 hour.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100272083A CN100336777C (en) | 2005-06-28 | 2005-06-28 | Method for preparing lutecia based transparent ceramics |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CNB2005100272083A CN100336777C (en) | 2005-06-28 | 2005-06-28 | Method for preparing lutecia based transparent ceramics |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| CN1760157A true CN1760157A (en) | 2006-04-19 |
| CN100336777C CN100336777C (en) | 2007-09-12 |
Family
ID=36706403
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CNB2005100272083A Expired - Fee Related CN100336777C (en) | 2005-06-28 | 2005-06-28 | Method for preparing lutecia based transparent ceramics |
Country Status (1)
| Country | Link |
|---|---|
| CN (1) | CN100336777C (en) |
Cited By (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1867618A1 (en) * | 2006-06-14 | 2007-12-19 | Schott AG | Optical elements as well as mapping optics |
| EP1867617A1 (en) * | 2006-06-14 | 2007-12-19 | Schott AG | Opto-ceramics, optical elements prepared therefrom as well as mapping optics |
| CN102557598A (en) * | 2011-03-21 | 2012-07-11 | 上海大学 | Pressureless sintering preparation method of Ce:Lu2SiO5 polycrystal flicker optical ceramics |
| CN103058256A (en) * | 2012-09-22 | 2013-04-24 | 包头市京瑞新材料有限公司 | Method for preparing large-granule dysprosium oxide |
| CN103058254A (en) * | 2012-09-22 | 2013-04-24 | 包头市京瑞新材料有限公司 | Preparation method of large-particle lutetium oxide |
| CN105236980A (en) * | 2015-11-19 | 2016-01-13 | 中国工程物理研究院化工材料研究所 | ZrO2-LiF-codoped vacuum sintering method for lutetium oxide transparent ceramic |
| CN106145959A (en) * | 2016-07-10 | 2016-11-23 | 九江学院 | A kind of preparation method of luteium oxide crystalline ceramics |
| CN106588014A (en) * | 2016-12-19 | 2017-04-26 | 中国科学院长春光学精密机械与物理研究所 | Luminescence enhanced Tm<3+>-doped Lu2O3-based transparent ceramic and preparation method thereof |
| CN108751991A (en) * | 2018-08-17 | 2018-11-06 | 徐州市江苏师范大学激光科技有限公司 | A kind of laser sintered preparation Tb:Lu2O3The method of ceramics |
| CN110256074A (en) * | 2019-07-16 | 2019-09-20 | 上海应用技术大学 | A kind of yttrium stablizes terbium oxide powder, magneto-optic crystalline ceramics and preparation method thereof |
| CN111138192A (en) * | 2020-01-03 | 2020-05-12 | 上海应用技术大学 | Vacuum hot-pressing preparation method of lutetium terbium oxide magneto-optical transparent ceramic |
| CN112853489A (en) * | 2021-01-06 | 2021-05-28 | 安徽工业大学 | Rare earth ion doped sesquioxide visible laser crystal material |
| CN114988876A (en) * | 2022-06-24 | 2022-09-02 | 中国工程物理研究院化工材料研究所 | Eu and Sc co-doped transparent lutetium oxide ceramic and preparation method thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4506090B2 (en) * | 2003-03-25 | 2010-07-21 | 株式会社村田製作所 | Dielectric ceramic and multilayer ceramic capacitors |
-
2005
- 2005-06-28 CN CNB2005100272083A patent/CN100336777C/en not_active Expired - Fee Related
Cited By (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1867618A1 (en) * | 2006-06-14 | 2007-12-19 | Schott AG | Optical elements as well as mapping optics |
| EP1867617A1 (en) * | 2006-06-14 | 2007-12-19 | Schott AG | Opto-ceramics, optical elements prepared therefrom as well as mapping optics |
| JP2007332023A (en) * | 2006-06-14 | 2007-12-27 | Schott Ag | Optical ceramic, optical element prepared from the optical ceramic, and mapping optics |
| US7700510B2 (en) | 2006-06-14 | 2010-04-20 | Schott Ag | Opto-ceramics made from In2O3 or oxides Y, Lu, Sc, Yb, In, Gd, and La, optical elements made therefrom, and mapping optics including the optical elements |
| US7751123B2 (en) | 2006-06-14 | 2010-07-06 | Schott Ag | Optical elements made from ceramics comprising one or more oxides of Y, Sc, in and/or lanthanide elements and mapping optics including the optical elements |
| CN102557598A (en) * | 2011-03-21 | 2012-07-11 | 上海大学 | Pressureless sintering preparation method of Ce:Lu2SiO5 polycrystal flicker optical ceramics |
| CN102557598B (en) * | 2011-03-21 | 2014-10-01 | 上海大学 | Pressureless sintering preparation method of Ce:Lu2SiO5 polycrystal flicker optical ceramics |
| CN103058256A (en) * | 2012-09-22 | 2013-04-24 | 包头市京瑞新材料有限公司 | Method for preparing large-granule dysprosium oxide |
| CN103058254A (en) * | 2012-09-22 | 2013-04-24 | 包头市京瑞新材料有限公司 | Preparation method of large-particle lutetium oxide |
| CN103058256B (en) * | 2012-09-22 | 2014-12-17 | 包头市京瑞新材料有限公司 | Method for preparing large-granule dysprosium oxide |
| CN105236980A (en) * | 2015-11-19 | 2016-01-13 | 中国工程物理研究院化工材料研究所 | ZrO2-LiF-codoped vacuum sintering method for lutetium oxide transparent ceramic |
| CN106145959A (en) * | 2016-07-10 | 2016-11-23 | 九江学院 | A kind of preparation method of luteium oxide crystalline ceramics |
| CN106588014A (en) * | 2016-12-19 | 2017-04-26 | 中国科学院长春光学精密机械与物理研究所 | Luminescence enhanced Tm<3+>-doped Lu2O3-based transparent ceramic and preparation method thereof |
| CN106588014B (en) * | 2016-12-19 | 2019-08-23 | 中国科学院长春光学精密机械与物理研究所 | A kind of Tm of luminescence enhancement3+Adulterate lutecia based transparent ceramics and preparation method |
| CN108751991A (en) * | 2018-08-17 | 2018-11-06 | 徐州市江苏师范大学激光科技有限公司 | A kind of laser sintered preparation Tb:Lu2O3The method of ceramics |
| CN108751991B (en) * | 2018-08-17 | 2020-03-13 | 徐州华焰特种陶瓷有限公司 | Preparation of Tb: Lu by laser sintering2O3Method for producing ceramic |
| CN110256074A (en) * | 2019-07-16 | 2019-09-20 | 上海应用技术大学 | A kind of yttrium stablizes terbium oxide powder, magneto-optic crystalline ceramics and preparation method thereof |
| CN111138192A (en) * | 2020-01-03 | 2020-05-12 | 上海应用技术大学 | Vacuum hot-pressing preparation method of lutetium terbium oxide magneto-optical transparent ceramic |
| CN112853489A (en) * | 2021-01-06 | 2021-05-28 | 安徽工业大学 | Rare earth ion doped sesquioxide visible laser crystal material |
| CN114988876A (en) * | 2022-06-24 | 2022-09-02 | 中国工程物理研究院化工材料研究所 | Eu and Sc co-doped transparent lutetium oxide ceramic and preparation method thereof |
| CN114988876B (en) * | 2022-06-24 | 2023-05-12 | 中国工程物理研究院化工材料研究所 | Eu and Sc co-doped transparent lutetium oxide ceramic and preparation method thereof |
Also Published As
| Publication number | Publication date |
|---|---|
| CN100336777C (en) | 2007-09-12 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CN100336777C (en) | Method for preparing lutecia based transparent ceramics | |
| CN104557041B (en) | Preparation method of yttria-base transparent ceramic | |
| CN101993240B (en) | Preparation method of Ce3+doped lutetium silicate (Lu2SiO5) polycrystalline flashing optical ceramic | |
| CN101333110B (en) | Method for preparing Nd<3+> -doped Lu2O3transparent laser ceramic | |
| CN110629288B (en) | Method for preparing whisker-shaped gadolinium aluminate powder material by hydrothermal technology | |
| CN101269964A (en) | Method for preparing yttrium oxide transparent ceramic | |
| CN101580393B (en) | Preparation method of transparent yttrium hafnate ceramics | |
| Li et al. | Up-conversion luminescence of new phosphors of Gd3Al5O12: Yb/Er stabilized with Lu3+ | |
| CN103214018B (en) | Preparation method for rare earth oxide nanosheet sol with positive charge | |
| CN1256300C (en) | Process for preparing yttrium oxide based transparent ceramic material | |
| CN108358635A (en) | A kind of preparation method of magneto-optic holimium oxide crystalline ceramics | |
| CN104341152A (en) | Preparation method for garnet phase nano-powder | |
| CN1275903C (en) | Textured columbate leadless piezoelectric materials and method for making same | |
| CN107445608B (en) | Method for preparing ZnO transparent ceramic by adopting discharge plasma sintering process | |
| CN103011806B (en) | In-situ preparation method of ferroelectric-dielectric composite ceramic material | |
| CN110550945B (en) | Preparation method of LuAG Ce transparent ceramic and LuAG Ce transparent ceramic | |
| CN107523298B (en) | Yttrium cerium composite oxide based up-conversion luminescent material and preparation method thereof | |
| CN113549458B (en) | High-color-rendering trivalent Eu ion-doped red fluorescent material based on apatite structure and preparation method thereof | |
| CN101648726B (en) | Hydrothermal synthesis method of LuO(OH) nanorods and Lu2O3 nanorods luminescent powder | |
| Li et al. | Photoluminescence properties of (Y1− xCex) 3Al5O12 (x= 0.005–0.03) nanophosphors and transparent ceramic by a homogeneous co-precipitation method | |
| CN1760327A (en) | Nano fluorophor powder based on lutecium oxide and synthetic method of solution burning thereof | |
| CN102701723A (en) | Preparation method of Ce-doped LaAlO3 flickering ceramic material | |
| CN111253152B (en) | Fast-attenuation high-light-efficiency scintillation material and preparation method thereof | |
| CN1609045A (en) | Prepn process of non-aggregate nanometer doped YAG powder | |
| CN101838849B (en) | Preparation method of CuAlO2 monocrystal |
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 | ||
| ASS | Succession or assignment of patent right |
Owner name: NINGBO YUNSHENG PHOTO-COMMUNICATION TECHNOLOGY CO. Free format text: FORMER OWNER: SHANGHAI INSTITUTE OF CERAMICS, CHINESE ACADEMY OF SCIENCES Effective date: 20100604 |
|
| C41 | Transfer of patent application or patent right or utility model | ||
| COR | Change of bibliographic data |
Free format text: CORRECT: ADDRESS; FROM: 200050 NO.1295, DINGXI ROAD, SHANGHAI CITY TO: 315000 NO.1, YANGFAN ROAD, NATIONAL NEW+HIGH-TECH ZONE, NINGBO CITY |
|
| TR01 | Transfer of patent right |
Effective date of registration: 20100604 Address after: 315000, No. 1, sailing Road, Ningbo national hi tech Zone Patentee after: Ningbo Yunsheng Photo-Communication Technology Co. Ltd. Address before: 1295 Dingxi Road, Shanghai, No. 200050 Patentee before: Shanghai Silicates Institute, the Chinese Academy of Sciences |
|
| CF01 | Termination of patent right due to non-payment of annual fee | ||
| CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20070912 Termination date: 20190628 |