CN113880588B - Method for preparing uniformly coated AlON powder and transparent ceramic thereof - Google Patents
Method for preparing uniformly coated AlON powder and transparent ceramic thereof Download PDFInfo
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Abstract
The invention relates to a method for preparing uniformly coated AlON powder and transparent ceramics thereof, which mainly comprises the following steps: the method comprises the steps of taking deionized water as a dispersion medium, adopting a chemical precipitation method based on the heterogeneous nucleation theory to deposit a compact sintering aid or a precursor of an activator on the surface of AlON powder subjected to hydrolysis resistance treatment by phosphoric acid in a non-homogeneous nucleation way, and sintering the AlON powder coated uniformly at 1780-1950 ℃ for several hours to obtain the AlON high-transparency ceramic. Compared with the traditional introduction mode, the method can improve the uniformity of the sintering aid or the activator in the AlON ceramic, effectively avoid differential sintering, inhibit abnormal growth of crystal grains and generation of intracrystalline pores caused by the abnormal growth of the crystal grains, and reduce the precipitation of a second phase so as to improve the transparency and improve the doping concentration of the activated ions. The method has the advantages of simple process, health, environmental protection, strong repeatability and relatively low sintering temperature, and the prepared AlON transparent ceramic has high optical transmittance, good mechanical property and high luminous efficiency.
Description
Technical Field
The invention relates to a method for preparing uniformly coated AlON powder and transparent ceramic thereof, belonging to the field of transparent ceramic and solid illumination/display.
Background
The aluminum oxynitride (AlON) transparent ceramic not only has the excellent characteristics of high hardness, high strength, good chemical stability and the like, but also has excellent optical transmittance in the near ultraviolet-middle infrared wavelength range (0.2-6 mu m), and the theoretical transmittance of the aluminum oxynitride transparent ceramic exceeds 85 percent. AlON structural transparent ceramics have been considered as a preferred material for high temperature infrared windows, missile hoods and bullet proof transparent armors. The AlON fluorescent transparent ceramic doped with the active ions also becomes a high-power solid-state lighting/displaying fluorescent material with very high potential.
At present, the transparent ceramics with AlON structure is mainly prepared by adopting a two-step method, namely synthesizing AlON powder and then sintering at high temperature. In order to enhance the optical transmittance by promoting the densification as much as possible, a small amount of a sintering aid is generally added to the AlON powder. The sintering aid is generally introduced by the following method: oxide, carbonate or nitrate containing sintering aid ions is added into AlON powder, and wet ball milling mixing is carried out by taking absolute ethyl alcohol or deionized water and the like as a dispersion medium [ Y.Shan et al.Script.Mater.,2018,157,148-151], [ Wangjun et al, CN201310491922.2,2013]. The introduction method using such wet ball milling is simple and convenient, however, even if the particle size of the sintering aid particles is reduced or soluble nitrate is used, it is still difficult to ensure uniform distribution of the sintering aid. In addition, when the colloidal forming technique is used, the surface characteristics of AlON and sintering aid are considered synergistically, otherwise uniform suspension is difficult to achieve. The differential sintering of the AlON ceramic in the heating and heat preservation process is easy to occur due to the uneven distribution of the sintering aids. On one hand, in a partial area where the sintering aid is absent, due to the lack of mass transfer effects such as inhibiting the movement of a grain boundary and promoting the diffusion of the grain boundary or volume diffusion, the growth of grains is easy to be too fast, so that intracrystalline pores which are difficult to discharge are formed; on the other hand, in a partial region where the sintering aid is excessive, the content may be too high to easily generate a second phase at the grain boundary, resulting in an influence on the optical transmission performance. For the preparation of the AlON fluorescent transparent ceramic, an appropriate amount of oxide, carbonate or nitrate containing active ions, which can also be used as a sintering aid per se, is generally added into AlON powder to perform wet ball milling [ zhangfang et al, CN200910247864.2,2009], so that the above problems are also generated, and more importantly, the uneven distribution of the active ions may generate concentration quenching due to too high local concentration, which seriously affects the luminescence effect.
Disclosure of Invention
Aiming at the problems caused by the difficulty in uniform distribution of the sintering aid or the activating ion-containing substance in the AlON powder in the traditional adding mode, the invention aims to provide a method for uniformly coating the sintering aid or the activating ion-containing AlON powder by a chemical precipitation method, and the powder can be used for preparing AlON high-transparency ceramic.
In order to realize the purpose, the technical scheme of the invention is as follows: a method for preparing uniformly coated AlON powder and transparent ceramics thereof is characterized by comprising the following steps:
(1) Weighing a proper amount of AlON powder, putting the AlON powder into a phosphoric acid solution with the concentration of 0.5-3wt.%, magnetically stirring for 10-30min at normal temperature, centrifugally filtering and drying to obtain hydrolysis-resistant hydrophilic AlON powder, wherein the mass ratio of the AlON powder to the phosphoric acid solution is 1;
(2) Mixing the AlON powder obtained in the step (1) with deionized water and a dispersing agent, and performing ultrasonic dispersion for 10-30min to obtain a highly dispersed suspension, wherein the mass ratio of AlON to deionized water is 1;
(3) Weighing nitrate of M ions and dissolving the nitrate in deionized water to obtain a solution A, wherein: m ion is Mg 2+ 、Ca 2+ 、Sr 2 + 、Ba 2+ 、Mn 2+ 、Sc 3+ 、Y 3+ 、La 3+ 、Ce 3+ 、Eu 3+ 、Pr 3+ 、Sm 3+ 、Gd 3+ 、Tb 3+ 、Dy 3+ 、Ho 3+ 、Er 3+ 、Tm 3+ 、Yb 3+ 、Lu 3+ 、Zr 4 + One or more of the solutions, wherein the purity of the nitrate is more than 99%, and the mass of the oxide converted by the nitrate is 0.04-0.7 wt% of AlON powder, and then the solution A is poured into the suspension obtained in the step (2) to form a suspension B, wherein the mass ratio of AlON in the suspension B to deionized water is 1;
(4) Preparing 0.002-0.2 mol/l of precipitator solution C, dropwise adding the precipitator solution C into the suspension B at the speed of 1-10ml/min, violently stirring in the dropwise adding process until the PH reaches a set value or the precipitator is excessive, then continuously stirring for 1-4h, carrying out centrifugal washing and drying to obtain AlON powder uniformly coated with M ions, wherein: the solution C is one of ammonia water, ammonium carbonate and ammonium phosphate solution;
(5) Forming the AlON powder obtained in the step (4), and removing glue in the air at 650 ℃ for 1-10h to obtain an AlON biscuit;
(6) Placing the AlON biscuit obtained in the step (5) in N 2 Sintering at 1780-1950 deg.C for 1-12h, cooling with furnace, grinding, and polishing to obtain AlON transparent ceramic.
According to the scheme, the molecular formula of AlON in the step (1) is Al (64+x)/3 O 32-x N x Wherein x is more than or equal to 2.5 and less than or equal to 5, and the average particle size of the powder is less than 3 mu m.
According to the scheme, the dispersing agent in the step (2) is one of PEG2000, ammonium polyacrylate and ammonium polymethacrylate, and the content of the dispersing agent accounts for 0.1-2 wt% of the AlON powder.
According to the scheme, the forming in the step (5) is one of dry pressing forming, slip casting forming and gel injection molding forming, wherein cold isostatic pressing forming is needed after the dry pressing forming is adopted.
According to the scheme, the sintering in the step (6) is one of pressureless sintering, hot-pressing sintering and spark plasma sintering, or one of the sintering and the hot isostatic pressing sintering are combined for use.
The principle of the invention is as follows: in order to prepare AlON suspension liquid taking deionized water as a dispersion medium, firstly, phosphoric acid hydrolysis resistance treatment is carried out on AlON powder, then, based on the non-uniform nucleation theory, a chemical precipitation method is adopted, and the thickness and chemical components of a uniform coating layer are accurately regulated and controlled by adjusting the concentration of a sintering aid or an activated ion and the dropping rate of a precipitator solution, so that a compact precursor which can be decomposed into the sintering aid or an activator is uniformly deposited on the surface of AlON particles. The uniformly distributed sintering aid or activator can effectively avoid differential sintering in the sintering process, inhibit the formation of crystal pores and reduce the formation of a second phase caused by over-fast growth of local crystal grains.
The invention has the beneficial results that:
1. the method adopts a chemical precipitation method to uniformly coat AlON powder, takes deionized water as a dispersion medium, is healthy and environment-friendly, and has strong operability; 2. the prepared AlON ceramic has high transparency, fine crystal grains, small internal stress and high strength; 3. the sintering temperature of the AlON transparent ceramic is relatively low, and the time is short; 4. the prepared AlON fluorescent transparent ceramic has high quenching concentration and high luminous efficiency; 5. the method has simple process and strong repeatability, and is beneficial to preparing large-size transparent ceramics.
Drawings
FIG. 1 is a scanning electron micrograph of AlON transparent ceramic prepared in example 1 of the present invention.
FIG. 2 is a graph showing the in-line transmittance of AlON transparent ceramic obtained in example 1 of the present invention.
FIG. 3 is a photograph of an AlON transparent ceramic prepared in example 1 of the present invention.
Detailed Description
For a better understanding of the present invention, the following description is further illustrated with reference to the accompanying drawings and examples, but the present invention is not limited to the following examples.
Example 1:
weighing 10g of self-made AlON powder, adding the self-made AlON powder into 200g of phosphoric acid solution with the concentration of 0.5wt.%, magnetically stirring for 10 minutes, centrifugally filtering at the speed of 3000r/min, and air-drying for 24 hours at the temperature of 40 ℃. Mixing the dried powder with 30g of deionized water and 0.01g of dispersant ammonium polymethacrylate, magnetically stirring, and adding 0.07g of prepared Y with equivalent mass 2 O 3 Y (NO) of 3 ) 3 And (3) maintaining the mass ratio of the final AlON powder to the deionized water to be 1. 0.2mol/l aqueous ammonia solution was then added dropwise at a rate of 10ml/min to the vigorously stirred suspension, the dropwise addition was stopped at pH =9.2 and stirring was continued for 2h to ensure complete precipitation. The suspension was washed 3 times by centrifugal filtration at 3000r/min and dried at 70 ℃ for 24 hours. Taking a proper amount of dried AlON powder, adding PVA with the mass of 1wt.% of the AlON powder for granulation, performing dry pressing at 20MPa to obtain a biscuit, performing cold isostatic pressing at 200MPa, and discharging glue in air at 650 ℃ for 5 hours. At 0.1MPa N 2 Under protection, the temperature is raised to 1880 ℃ at the heating rate of 10 ℃/min, pressureless sintering is carried out for 12h, and furnace cooling is carried out. And cutting, grinding and polishing the cooled sintered body to obtain the AlON structure transparent ceramic.
The AlON transparent ceramic obtained in this example was subjected to SEM test (see fig. 1), and fig. 1 illustrates: the prepared material is mainly isometric crystal, the average grain size is about 102 mu m, and almost no air holes exist.
The transmittance test was performed (see fig. 2), fig. 2 illustrates: the linear transmittance of a sample with the thickness of 4mm at 600nm measured by an ultraviolet-visible spectrophotometer is 77%. The microhardness is 16.2GPa and the fracture toughness is 2.3 MPa.m measured by an indentation method 1/2 。
Example 2:
weighing 20g of self-made AlON powder, adding 40g of phosphoric acid solution with the concentration of 3wt.%, magnetically stirring for 30 minutes, centrifugally filtering at the speed of 3000r/min, and drying by air blast at 40 ℃ for 24 hours. Mixing the dried powder with 60g deionized water and 0.4g dispersant PEG2000, magnetically stirring, and adding 0.04gY 2 O 3 And 0.16g La 2 O 3 Y (NO) of 3 ) 3 And La (NO) 3 ) 3 And (3) mixing the solution, wherein the mass ratio of the final AlON powder to the deionized water is 1. 0.002mol/l aqueous ammonia solution was then added dropwise at a rate of 1ml/min to the vigorously stirred suspension, stopping the addition when the pH =9.1, and stirring was continued for 4h to ensure complete precipitation. The suspension was washed 3 times by centrifugal filtration at 3000r/min and dried at 70 ℃ for 24 hours. Taking 10g of dried AlON powder, 15g of deionized water, 0.3g of monomer acrylamide, 0.03g of cross-linking agent N, N' -methylene acrylamide and 0.2g of dispersing agent PEG20000.2g, and magnetically stirring for 2h. And (3) degassing the obtained slurry in vacuum, adding 0.03g of initiator ammonium persulfate, stirring uniformly, pouring into a mould, and curing for 3 hours at 70 ℃. The demoulded biscuit is dried for 2 days at 50 ℃ and then is subjected to gel removal in air at 650 ℃ for 10 hours. At 0.1MPaN 2 Under the protection, the temperature is raised to 1800 ℃ at the heating rate of 10 ℃/min, pressureless sintering is carried out for 2h, then hot isostatic pressing is carried out for 4h at 1850 ℃, and the pressure is 200MPa. And cutting, grinding and polishing the cooled sintered body to obtain the AlON structure transparent ceramic.
The ceramic sample having an average crystal grain size of 48 μm and a thickness of 4mm was measured to have a linear transmittance at 600nm of 81%, a microhardness of 16.4GPa, and a fracture toughness of 2.5MPa m 1/2 。
Example 3:
weighing 20g of self-made AlON powder, adding the self-made AlON powder into 100g of phosphoric acid solution with the concentration of 1wt.%, magnetically stirring for 10 minutes, centrifugally filtering at the speed of 3000r/min, and drying by air blowing at 40 ℃ for 24 hours. Mixing the dried powder with 80gDeionized water and 0.1g dispersant ammonium polymethacrylate are mixed and stirred by magnetic force, and then Sr (NO) with the same mass as 0.2g SrO is added 3 ) 2 And (3) keeping the mass ratio of the final AlON powder to the deionized water to be 1. 0.1mol/l ammonium carbonate solution was then added dropwise at a rate of 5ml/min to the vigorously stirred suspension, the dropwise addition being stopped when the precipitant was in excess and stirring continued for 4h. The suspension was washed 3 times by centrifugal filtration at 3000r/min and dried at 70 ℃ for 24h. Taking 10g of dried AlON powder, 20g of deionized water and 0.1g of dispersant ammonium polymethacrylate, magnetically stirring for 2h, degassing in vacuum, and pouring porous Al 2 O 3 Drying in ceramic mold at room temperature for 24 hr, demolding, and drying at 60 deg.C for 24 hr to obtain biscuit of 0.1MPaN 2 Pressureless sintering for 8h under the protection of 1920 ℃, and then cooling along with the furnace. And cutting, grinding and polishing the cooled sintered body to obtain the AlON structure transparent ceramic.
The ceramic has an average grain size of 87 μm, a linear transmittance at 600nm of a sample with a thickness of 4mm of 79%, a microhardness of 16.3GPa, and a fracture toughness of 2.2 MPa-m 1/2 。
Example 4:
weighing 20g of self-made AlON powder, adding the self-made AlON powder into 100g of phosphoric acid solution with the concentration of 2wt.%, magnetically stirring for 10 minutes, centrifugally filtering at the speed of 3000r/min, and air-drying for 24 hours at the temperature of 40 ℃. Mixing the dried powder with 100g deionized water and 0.1g dispersant ammonium polyacrylate, magnetically stirring, and adding 0.1g CaO-containing Ca (NO) 3 ) 2 And (3) keeping the mass ratio of the final AlON powder to the deionized water to be 1. 0.1mol/l ammonium phosphate solution is then added dropwise at a rate of 2ml/min to the vigorously stirred suspension, the dropwise addition being stopped when the precipitant is in excess, and stirring is continued for 4h. The suspension was washed 3 times by centrifugal filtration at 3000r/min and dried at 70 ℃ for 24 hours. Carbon is removed in air for 1h at 650 ℃. Taking appropriate amount of dried AlON powder at 0.1MPaN 2 Hot-pressing and sintering at 1820 ℃ for 1h under the protection of 30MPa, and then cooling along with the furnace. And cutting, grinding and polishing the cooled sintered body to obtain the AlON structure transparent ceramic.
The ceramic has an average grain size of 28 μm and a thickness of 4mmThe sample (2) had a straight-line transmittance at 600nm of 71%, a microhardness of 16.2GPa, and a fracture toughness of 2.7 MPa.m 1/2 。
Example 5:
weighing 20g of self-made AlON powder, adding 50g of phosphoric acid solution with the concentration of 1wt.%, magnetically stirring for 20 minutes, centrifugally filtering at the speed of 3000r/min, and drying by air blowing at 40 ℃ for 24 hours. Mixing the dried powder with 60g deionized water and 0.3g dispersant PEG2000, magnetically stirring, and adding 0.004g Eu 2 O 3 Eu (NO) 3 ) 3 And (3) maintaining the mass ratio of the final AlON powder to the deionized water to be 1. 0.2mol/l aqueous ammonia solution was then added dropwise at a rate of 1ml/min to the vigorously stirred suspension, the dropwise addition was stopped at pH =9.3 and stirring was continued for 4h to ensure complete precipitation. The suspension was washed 3 times by centrifugal filtration at 3000r/min and dried at 70 ℃ for 24 hours. Taking a proper amount of dried AlON powder, dry-pressing into a biscuit at 20MPa, then carrying out cold isostatic pressing at 200MPa, and removing carbon in air at 650 ℃ for 1h. At 0.1MPa N 2 Under protection, the temperature is raised to 1950 ℃ at the heating rate of 15 ℃/min, pressureless sintering is carried out for 12 hours, and furnace cooling is carried out. And cutting, grinding and polishing the cooled sintered body to obtain the AlON fluorescent transparent ceramic.
The measurement shows that the ceramic block has an average grain size of 106 μm, the linear transmittance at 600nm of a sample with the thickness of 4mm is 72%, the peak wavelength of an emission spectrum is 490nm, the microhardness is 16.0GPa, and the fracture toughness is 2.1 MPa.m 1/2 。
Example 6:
weighing 20g of self-made AlON powder, adding the self-made AlON powder into 100g of phosphoric acid solution with the concentration of 2wt.%, magnetically stirring for 10 minutes, centrifugally filtering at the speed of 3000r/min, and drying by air blowing at 40 ℃ for 24 hours. Mixing the dried powder with 100g deionized water and 0.2g dispersant ammonium polyacrylate, magnetically stirring, and adding 0.1g MgO and 0.04g MnO Mg (NO) 3 ) 2 And Mn (NO) 3 ) 2 And mixing the solution, and keeping the mass ratio of the final AlON powder to the deionized water to be 1. Then 0.01mol/l ammonia solution was added dropwise at a dropping rate of 5ml/min to the vigorously stirred suspension, stopping the addition when the PH =9.3, and stirring was continued for 4h. The suspension is heated to 3Washed 3 times by centrifugal filtration at a speed of 000r/min and dried for 24 hours at 70 ℃. Carbon is removed in air for 1h at 650 ℃. Taking appropriate amount of dried AlON powder at 0.1MPaN 2 Under protection, the plasma is discharged at 1780 ℃ at the heating rate of 100 ℃/min for rapid sintering for 10min, and the pressure is 30MPa. And cutting, grinding and polishing the cooled sintered body to obtain the AlON fluorescent transparent ceramic.
The ceramic sample with the average grain size of 7 mu m and the thickness of 4mm has the linear transmittance of 52 percent at 600nm, the peak wavelength of the emission spectrum of 512nm, the microhardness of 16.6GPa and the fracture toughness of 3.0 MPa-m 1/2 。
Example 7:
weighing 20g of self-made AlON powder, adding the self-made AlON powder into 100g of phosphoric acid solution with the concentration of 2wt.%, magnetically stirring for 10 minutes, centrifugally filtering at the speed of 3000r/min, and drying by air blowing at 40 ℃ for 24 hours. Mixing the dried powder with 100g of deionized water and 0.2g of dispersant ammonium polyacrylate, magnetically stirring, and adding 0.02g of prepared Er 2 O 3 And 0.03g Yb 2 O 3 Er (NO) of 3 ) 3 And Yb (NO) 3 ) 3 And (3) mixing the solution, and keeping the mass ratio of the final AlON powder to the deionized water to be 1. 0.01mol/l aqueous ammonia solution was then added dropwise at a rate of 5ml/min to the vigorously stirred suspension, the dropwise addition was stopped at pH =9.3 and stirring was continued for 4h. The suspension was washed 3 times by centrifugal filtration at 3000r/min and dried at 70 ℃ for 24 hours. Taking a proper amount of dried AlON powder, adding PVA (polyvinyl alcohol) with the mass of 1wt.% of the AlON powder for granulation, performing dry pressing at 20MPa to form a biscuit, performing cold isostatic pressing at 200MPa, and discharging glue in air at 650 ℃ for 5 hours. At 0.1MPaN 2 Under the protection, the temperature is raised to 1900 ℃ at the heating rate of 10 ℃/min, pressureless sintering is carried out for 8h, and furnace cooling is carried out. And cutting, grinding and polishing the cooled sintered body to obtain the AlON fluorescent transparent ceramic.
The ceramic material was measured to have an average crystal grain size of 123 μm, a linear transmittance at 600nm of a 4mm thick sample of 63%, a peak wavelength of emission spectrum under 980nm laser irradiation of 655nm, a microhardness of 15.9GPa, and a fracture toughness of 2.0 MPa.m 1 /2 。
Claims (5)
1. A method for preparing uniformly coated AlON powder and transparent ceramics thereof is characterized by comprising the following steps:
(1) Weighing a proper amount of AlON powder, putting the AlON powder into a phosphoric acid solution with the concentration of 0.5-3wt.%, magnetically stirring for 10-30min at normal temperature, centrifugally filtering and drying to obtain hydrolysis-resistant hydrophilic AlON powder, wherein the mass ratio of the AlON powder to the phosphoric acid solution is 1;
(2) Mixing the AlON powder obtained in the step (1) with deionized water and a dispersing agent, and performing ultrasonic dispersion for 10-30min to obtain a highly dispersed suspension, wherein the mass ratio of AlON to deionized water is 1;
(3) Weighing nitrate of M ions and dissolving the nitrate in deionized water to obtain a solution A, wherein: m ion is Mg 2+ 、Ca 2+ 、Sr 2+ 、Ba 2 + 、Mn 2+ 、Sc 3+ 、Y 3+ 、La 3+ 、Ce 3+ 、Eu 3+ 、Pr 3+ 、Sm 3+ 、Gd 3+ 、Tb 3+ 、Dy 3+ 、Ho 3+ 、Er 3+ 、Tm 3+ 、Yb 3+ 、Lu 3+ 、Zr 4+ One or more nitrate(s) with the purity of more than 99% and the oxide mass converted from the nitrate(s) is 0.04-0.7 wt% of AlON powder, and then the solution A is poured into the suspension obtained in the step (2) to form a suspension B, wherein the mass ratio of AlON to deionized water in the suspension B is 1;
(4) Preparing 0.002-0.2 mol/l of precipitator solution C, dropwise adding the precipitator solution C into the suspension B at the speed of 1-10ml/min, violently stirring in the dropwise adding process until the PH reaches a set value or the precipitator is excessive, then continuously stirring for 1-4h, carrying out centrifugal washing and drying to obtain AlON powder uniformly coated with M ions, wherein: the solution C is one of ammonia water, ammonium carbonate and ammonium phosphate solution;
(5) Forming the AlON powder obtained in the step (4), and removing glue in the air at 650 ℃ for 1-10h to obtain an AlON biscuit;
(6) Placing the AlON biscuit obtained in the step (5) in N 2 Sintering at 1780-1950 deg.C for 1-12h, cooling with furnace, grinding, and polishing to obtain AlONAnd (3) bright ceramics.
2. The method for preparing the uniformly coated AlON powder and the transparent ceramic thereof according to claim 1, wherein the method comprises the following steps: the molecular formula of AlON in the step (1) is Al (64+x)/3 O 32-x N x Wherein x is more than or equal to 2.5 and less than or equal to 5, and the average particle size of the powder is less than 3 mu m.
3. The method for preparing the uniformly coated AlON powder and the transparent ceramic thereof as claimed in claim 1, wherein the method comprises the following steps: the dispersing agent in the step (2) is one of PEG2000, ammonium polyacrylate and ammonium polymethacrylate, and the content of the dispersing agent accounts for 0.1-2 wt% of the AlON powder.
4. The method for preparing the uniformly coated AlON powder and the transparent ceramic thereof as claimed in claim 1, wherein the method comprises the following steps: the forming in the step (5) is one of dry pressing, slip casting and gel injection molding, wherein cold isostatic pressing is needed after the dry pressing.
5. The method for preparing the uniformly coated AlON powder and the transparent ceramic thereof according to claim 1, wherein the method comprises the following steps: and (3) the sintering in the step (6) is pressureless sintering, hot pressing sintering or spark plasma sintering, or the sintering is combined with hot isostatic pressing sintering.
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| CN105732050A (en) * | 2016-01-13 | 2016-07-06 | 广东工业大学 | Preparation technology of net size transparent ceramic part in complex shape |
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| CN105732050A (en) * | 2016-01-13 | 2016-07-06 | 广东工业大学 | Preparation technology of net size transparent ceramic part in complex shape |
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