WO2010140644A1 - 高強度透明ジルコニア焼結体及びその製造方法、並びにその用途 - Google Patents
高強度透明ジルコニア焼結体及びその製造方法、並びにその用途 Download PDFInfo
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Definitions
- the present invention is transparent and excellent in mechanical strength, and relates to a titania-added transparent zirconia sintered body that can be used for timepiece parts, decorative members, electronic equipment exterior parts, aesthetic dental parts, and the like.
- Non-patent Document 1 Since the transparent zirconia sintered body has a high refractive index and a high dielectric constant, it is expected to be used as an optical member (Patent Document 1). In particular, since the transparent zirconia sintered body to which titania is added exhibits high transmittance, application to optical lenses and the like has been energetically studied (Non-patent Document 1 and Patent Document 2).
- zirconia sintered bodies have recently been examined for application to decorative parts and exterior parts. There is a demand for a titania-added zirconia sintered body having sufficient strength.
- the conventional titania-added transparent zirconia has translucency, but has insufficient mechanical strength.
- Patent Document 2 reports a zirconia sintered body having a measurement wavelength of 600 nm and a linear transmittance of 65% at a sample thickness of 0.8 mm. However, the crystal grain size was as large as about 100 ⁇ m and the mechanical strength was low. Non-Patent Document 2 discloses a titania-added transparent zirconia sintered body having a particle diameter of 200 ⁇ m, but its mechanical strength (bending strength) is as low as about 210 MPa.
- titania-added zirconia sintered body having both mechanical strength and high translucency and a method for producing the same have not been known.
- a transparent zirconia sintered body and the like having a linear transmittance of 72% (sample thickness of 1 mm) and the like are reported (Patent Documents 2, 4, and 5, and Non-Patent Document 1).
- these sintered bodies are so-called cloudy sintered bodies having a certain degree of translucency but having turbidity, and further transparency is required for optical applications.
- the manufacturing method disclosed in the cited document 1 has prepared the manufacturing atmosphere by the sample container installation method, it is necessary to stably control the atmosphere in a high-temperature HIP process accompanied by deformation of the container.
- titania-containing zirconia sintered body having excellent translucency and mechanical strength.
- yttria is 6 mol% to 15 mol% and titania is 3 mol% to 3 mol%.
- the inventors have found that a zirconia sintered body containing 20 mol% can obtain a sintered body having a sample thickness of 1 mm and a linear transmittance of 50% or more at a measurement wavelength of 600 nm, thereby completing the present invention.
- the gist of the present invention resides in the following (1) to (16).
- the zirconia sintered body according to (2) above, wherein the average bending strength is 250 MPa or more.
- the zirconia sintered body according to the above (1) having a linear transmittance of 73% or more and a haze ratio of 2.0% or less at a sample thickness of 1 mm and a measurement wavelength of 600 nm.
- the lightness L * is 84 or more and 90 or less, the zirconia sintered body according to (7) above, wherein (9) The zirconia according to (7), wherein the hue is preferably a * of ⁇ 1.5 to 0.2 and b * of 0.0 to 4.0. Sintered body. (10) After forming a zirconia powder containing 3 mol% to 20 mol% titania and 6 mol% to 15 mol% yttria, primary sintering is performed at normal pressure, and hot isostatic pressing (HIP) treatment is performed to obtain a Ti reduction ratio of 20 % Of sintered body, and the sintered body is annealed.
- HIP hot isostatic pressing
- a method for producing a zirconia sintered body containing 3 mol% to 20 mol% of titania and 6 mol% to 15 mol% of yttria (11) Preferably, the method for producing a zirconia sintered body according to (10) above, wherein the primary sintered body having a relative density of 94% or more and an average particle diameter of 3 ⁇ m or less is subjected to HIP treatment. (12) The method for producing a zirconia sintered body according to (10), wherein the sintered body sintered at 1200 ° C. to 1400 ° C. is preferably subjected to HIP treatment.
- the zirconia sintered body of the present invention has high translucency with a linear transmittance of 50% or more (sample thickness 1 mm and measurement wavelength 600 nm). Furthermore, it is preferable that the average bending strength has a high mechanical strength of 250 MPa or more.
- the zirconia sintered body having particularly high translucency has a linear transmittance of 73% or more (sample thickness of 1 mm and measurement wavelength of 600 nm) and a haze ratio of 2.0% or less and no turbidity (cloudiness). It has quality transparency. Compared with transparent materials such as glass and plastic, the refractive index and dielectric constant are remarkably high, infrared transmission of longer wavelengths, and excellent mechanical properties such as hardness, bending strength, and fracture toughness. is there.
- FIG. 1 is a view showing a sintered body structure (Example 6) of the present invention (scale in the figure is 10 ⁇ m).
- FIG. 2 is a graph showing the transmittance (Example 6) of the sintered body of the present invention.
- FIG. 3 is a view showing a schlieren image (Example 6) of the sintered body of the present invention.
- FIG. 4 is a view showing a schlieren image (Comparative Example 4) of a sintered body of a comparative example.
- FIG. 1 is a view showing a sintered body structure (Example 6) of the present invention (scale in the figure is 10 ⁇ m).
- FIG. 2 is a graph showing the transmittance (Example 6) of the sintered body of the present invention.
- FIG. 3 is a view showing a schlieren image (Example 6) of the sintered body of the present invention.
- FIG. 4 is a view showing a schlieren image (Comparative Example
- FIG. 5A is a diagram showing the result of SEM observation (10 h at 1300 ° C.) (9 mol% yttria and 10 mol% titania-containing zirconia) of the structure of the primary sintered body (scale in the figure is 5 ⁇ m).
- FIG. 5B is a diagram showing the results of SEM observation (2 h at 1400 ° C.) of the structure of the primary sintered body (9 mol% yttria and 10 mol% titania-containing zirconia) (scale in the figure is 5 ⁇ m).
- FIG. 5A is a diagram showing the result of SEM observation (10 h at 1300 ° C.) (9 mol% yttria and 10 mol% titania-containing zirconia) of the structure of the primary sintered body (scale in the figure is 5 ⁇ m).
- FIG. 5B is a diagram showing the results of SEM observation (2 h at 1400 ° C.) of the structure of the primary sintered body (9 mol
- 5C is a diagram showing the results of SEM observation (2 hours at 1500 ° C.) of the structure of the primary sintered body (9 mol% yttria and 10 mol% titania-containing zirconia) (scale in the figure is 10 ⁇ m).
- FIG. 6 is a graph showing the relationship between haze ratio and Ti reduction ratio.
- FIG. 7 is a graph showing the relationship between haze ratio and primary sintering temperature.
- the zirconia sintered body of the present invention contains 6 mol% to 15 mol%, preferably 8 mol% to 12 mol%, of yttria (Y 2 O 3 ).
- yttria Y 2 O 3
- the crystal phase of the zirconia sintered body can be made only to have a cubic fluorite structure.
- the yttria content is less than 6 mol%, tetragonal crystals are mixed in addition to cubic crystals, and when it exceeds 15 mol%, different crystal phases other than cubic crystals such as pyrochlore oxide (Y 2 Ti 2 O 7 ) are mixed. However, the translucency is lowered.
- the zirconia sintered body of the present invention contains 3 mol% to 20 mol% of titania (TiO 2 ), preferably 8 mol% to 15 mol%. If the titania content is less than 3 mol%, sufficient light transmission cannot be obtained. On the other hand, if it exceeds 20 mol%, a compound phase such as ZrTiO 4 is mixed, and the translucency is also lowered.
- titania TiO 2
- the zirconia sintered body of the present invention preferably contains both yttria and titania, which are dissolved in zirconia.
- the zirconia sintered body of the present invention preferably has a metal impurity of 10 ppm or less. If the metal impurity exceeds 10 ppm, the sintered body tends to be colored.
- the metal impurity include metals other than Ti, Y, and Zr, and examples thereof include Al, Fe, and Mg.
- the average bending strength is preferably 250 MPa or more, more preferably 260 MPa or more, further preferably 280 MPa or more, and particularly preferably 300 MPa or more. preferable. If it is less than 250 MPa, the zirconia sintered body tends to be damaged.
- the average crystal grain size of the zirconia sintered body having particularly high translucency is preferably 60 ⁇ m or less, more preferably 56 ⁇ m or less. Moreover, as a lower limit, it is preferable that it is 30 micrometers or more, It is more preferable that it is 40 micrometers or more, It is still more preferable that it is 45 micrometers or more.
- the average crystal grain size of the zirconia sintered body having particularly high strength is preferably less than 30 ⁇ m, more preferably 25 ⁇ m or less, and further preferably 22 ⁇ m or less.
- the lower limit of the crystal grain size is not particularly limited, but is preferably 6 ⁇ m or more and more preferably 10 ⁇ m or more from the viewpoint of translucency.
- the zirconia sintered body of the present invention is dense without pores, and the sintered density is preferably 99.9% or more, more preferably 99.99% or more in terms of relative density. More preferably, it is 998% or more.
- the pore volume of the zirconia sintered body is preferably 0.002% by volume or less, and more preferably 0.001% by volume or less. When the amount of pores exceeds 0.002% by volume, the linear transmittance tends to be lowered.
- the crystal phase of the sintered body of the present invention is preferably cubic, and more preferably a cubic fluorite structure. Since cubic crystals do not have optical anisotropy, the transparency of the obtained sintered body is increased by making individual crystals of the polycrystalline body cubic. When a crystal phase having optical anisotropy such as tetragonal crystal is contained, the linear transmittance is likely to decrease.
- the zirconia sintered body of the present invention has a sample thickness of 1 mm and a linear transmittance at a measurement wavelength of 600 nm of 50% or more, preferably 60% or more, more preferably 65% or more, and further preferably 70% or more.
- a linear transmittance at a measurement wavelength of 600 nm 50% or more, preferably 60% or more, more preferably 65% or more, and further preferably 70% or more.
- the linear transmittance is more preferably 73% or more at a measurement wavelength of 600 nm at a sample thickness of 1 mm, and particularly preferably 73.5% or more.
- the linear transmittance is a parameter having the following relational expression.
- the sample thickness is preferably 1 mm and the haze ratio is preferably 2.0% or less, and more preferably 1.0% or less. If the haze ratio exceeds 2.0%, the sintered body becomes cloudy and is difficult to use for optical materials. On the other hand, the haze ratio is preferably as small as possible. However, if it is 2.0% or less, the transparency becomes sufficient for use in optical materials.
- the haze ratio H (%) can be obtained from the following relational expression.
- the zirconia sintered body of the present invention preferably has no striae. When striae occur, the translucency tends to decrease due to light scattering due to the difference in refractive index.
- the sintered body of the present invention preferably has a diffusion coefficient ⁇ of 0.15 cm ⁇ 1 or less at a measurement wavelength of 600 nm.
- a diffusion coefficient can be calculated
- the diffusion coefficient increases as the haze ratio increases. For example, if the haze ratio is 2.0% or less, the diffusion coefficient obtained by the equation (3) at a measurement wavelength of 600 nm is 0.15 cm ⁇ 1 or less.
- the average crystal grain size is preferably 30 ⁇ m or more and 60 ⁇ m or less.
- the sintered body of the present invention preferably has a lightness L * of 84 or more and 90 or less. By making the brightness within this range, the transparency of the sintered body is improved. When L * is less than 84, the lightness is too low and the transparency is lowered.
- the hue a * is ⁇ 1.5 or more and 0.2 or less and b * is 0.0 or more and 4.0 or less, the color of the sintered body is lost.
- the hue b * exceeds 4.0, the sintered body tends to be light yellowish.
- the sintered body of the present invention can be manufactured by molding a raw material powder containing zirconia, yttria, and titania, followed by primary sintering, followed by hot isostatic pressing (HIP) treatment and annealing.
- HIP hot isostatic pressing
- a powder containing zirconia, yttria, and titania is used as a raw material powder.
- the raw material powder is not particularly limited as long as it contains a predetermined amount of these components, but it is industrially advantageous to use a mixed powder obtained by mixing yttria solid solution zirconia powder and titania powder.
- the yttria solid solution zirconia powder used for the mixed powder is preferably a powder having a purity of 99.9% or more and a specific surface area of 5 m 2 / g to 20 m 2 / g. Further, the yttria solid solution zirconia powder is preferably a powder having an average crystallite size of 10 nm to 50 nm and an average secondary particle size of 100 nm to 500 nm, and more preferably a powder produced by a wet synthesis method such as a hydrolysis method. .
- the titania powder used for the mixed powder preferably has a purity of 99.9% or more and a specific surface area of 10 m 2 / g to 100 m 2 / g, a purity of 99.95% or more, an average crystallite diameter of 30 nm or less, and an average of 2
- a fine powder having a secondary particle size of 500 nm or less is more preferable.
- a powder produced by a sulfuric acid method or a gas phase pyrolysis method is more preferable.
- the method is not particularly limited as long as both are uniformly dispersed, but wet mixing such as a wet ball mill or a wet stirring mill is preferable because it can be mixed more uniformly.
- the raw material powder preferably has few metal impurities, for example, Fe 2 O 3 is preferably 10 ppm or less. When Fe 2 O 3 exceeds 10 ppm, the obtained zirconia sintered body is colored yellow.
- a raw material powder is molded to obtain a molded body for primary sintering.
- the raw material powder molding method is not limited as long as it can obtain a molded body having a shape suitable for primary sintering, and is generally used for ceramic molding, such as press molding and cold isostatic pressing.
- a molding method such as cast molding, extrusion molding, or injection molding can be used.
- a primary sintered body to be subjected to HIP treatment by primary sintering of the molded body is produced.
- the primary sintered body preferably has a relative density of 90% or more. If the relative density is less than 90%, the pores cannot be completely excluded in the HIP treatment, so that the density of the obtained zirconia sintered body does not increase and the translucency tends to be lowered.
- the relative density of the primary sintered body is preferably 94% or more.
- the sintered body includes open pores, and the HIP processing gas enters the inside of the sintered body, so that the density does not increase and the transmittance decreases.
- the average particle size of the sintered particles of the primary sintered body is preferably 10 ⁇ m or less, more preferably 3 ⁇ m or less, and even more preferably 2 ⁇ m or less.
- the translucency of the zirconia sintered body of the present invention strongly depends on the structure of the primary sintered body, and when the average particle size of the sintered particles of the primary sintered body exceeds 10 ⁇ m, The pores are likely to remain, and the pores are difficult to be excluded even after the HIP treatment. On the other hand, when the average particle size of the sintered particles is 10 ⁇ m or less, all the pores in the primary sintered body are present at the grain boundaries of the sintered particle size, and the pores are sufficiently excluded after the HIP treatment.
- the average particle size is 10 ⁇ m or less, plastic flow of the sintered particles is likely to occur during the HIP process, which is considered to be a cause of easily removing the pores.
- the average particle size is 3 ⁇ m or less, this effect tends to be remarkable.
- the transparency of the zirconia sintered body of the present invention strongly depends on the structure of the primary sintered body, particularly the presence of pores contained in the sintered body.
- As the existence form of pores contained in the primary sintered body two forms of grain boundary pores and intragranular pores are conceivable, but it is particularly preferable that no intragranular pores are contained. If the grain boundary pores exist between the crystal grains of the primary sintered body, even if they exist, they are likely to disappear by HIP treatment, and the influence on the transparency of the finally obtained sintered body is small.
- the crystal phase of the primary sintered body is preferably a mixed phase of a cubic phase and a tetragonal phase.
- the sintering temperature of primary sintering is preferably 1200 ° C. or higher and 1400 ° C. or lower, more preferably 1250 ° C. or higher and 1400 ° C. or lower, and further preferably 1300 ° C. or higher and 1375 ° C. or lower.
- the sintering temperature of primary sintering is lower than the HIP treatment temperature, preferably 1200 ° C. to 1400 ° C., more preferably 1250 ° C. to 1400 ° C.
- the temperature is preferably 1300 ° C to 1400 ° C.
- the temperature raising rate is preferably 100 ° C. to 300 ° C./h.
- the holding time of primary sintering varies depending on the sintering temperature and cannot be determined uniformly, but is in the range of about 1 to 10 hours. For example, when the sintering temperature is 1300 ° C., about 10 hours is preferable, and when the sintering temperature is higher than that, sintering can be performed in a short time of 1 hour to 5 hours. Primary sintering can be usually performed in the air, but sintering in an atmosphere such as oxygen or vacuum may be applied.
- the primary sintered body is next subjected to HIP treatment.
- the HIP treatment temperature is higher than the primary sintering temperature, preferably 1250 ° C. or higher and lower than 1600 ° C., more preferably 1275 ° C. or higher and 1550 ° C. or lower, and more preferably 1300 ° C. or higher and 1500 ° C. or lower. Further preferred. If the temperature is 1600 ° C. or higher, the sintered particle size becomes extremely coarse and the strength tends to decrease. However, at a temperature lower than 1250 ° C., even if HIP treatment is performed, the crystal phase of the primary sintered body in which cubic crystals and tetragonal crystals are mixed is not limited to cubic crystals, and the translucency of the resulting zirconia sintered body decreases. Cheap.
- the HIP treatment temperature is preferably 1400 ° C. or higher and 1800 ° C. or lower, more preferably 1550 ° C. to 1800 ° C., and further preferably 1600 ° C. to 1700 ° C.
- Transparency of the sintered body obtained by setting it as 1400 degreeC or more improves, and transparency improves further at 1550 degreeC or more.
- a temperature exceeding 1800 ° C. can be applied, the crystal grain size of the obtained zirconia sintered body becomes extremely large, so that the strength decreases.
- the zirconia sintered body of the present invention has higher transparency as the ratio of Ti 3+ in Ti contained in the sintered body during HIP treatment (hereinafter referred to as Ti reduction ratio) increases. This is considered to be due to the following mechanism.
- Ti reduction can be performed during either primary sintering or HIP treatment, but it is more preferably performed during HIP treatment.
- the Ti reduction ratio can be obtained by calculation assuming that the weight difference between the sintered body after HIP treatment and after annealing (oxidation) is an oxygen defect of titania.
- the weight difference between the sintered body after the HIP treatment and after annealing (oxidation) in the method of the present invention is a titania-derived reduction. It can be seen that it is.
- the Ti reduction ratio in the method of the present invention is preferably 20% or more, and more preferably 25% or more.
- the Ti reduction ratio is 20% or more, many oxygen vacancies are formed, the movement (disappearance) of residual pores is promoted, and a highly transparent zirconia sintered body is obtained.
- the Ti reduction ratio is less than 20%, the number of oxygen vacancies formed is small, and thus the removal of residual pores is difficult to proceed.
- the Ti reduction ratio is preferably 20% or more, more preferably 30% or more, and further preferably 40% or more. If the Ti reduction ratio is less than 20%, the translucency of the obtained zirconia sintered body is lowered.
- Ti reduction in HIP treatment is generated by the reaction of trace amounts of oxygen contained in HIP pressure media such as non-oxidizing gases such as argon and nitrogen, and carbon such as heaters and heat insulating materials in HIP equipment. It can be reduced using carbon monoxide.
- sample container a reducing material such as carbon is preferable.
- restoration is further accelerated
- a zirconia sintered body can be obtained by annealing the sintered body after the HIP treatment.
- the sintered body after the HIP treatment with a Ti reduction ratio of 20% or more exhibits a black color, it does not have sufficient transparency as it is.
- the sintered body can be oxidized by annealing to obtain a zirconia sintered body having high transparency and no turbidity (cloudiness).
- the annealing is preferably performed at a temperature of 1000 ° C. to 1200 ° C. for 1 hour or more and normal pressure in the atmosphere or an oxidizing atmosphere using oxygen.
- Ti reduction ratio The weight change of the sintered body after the HIP treatment and after annealing was measured, and the Ti 3+ content (z) and Ti reduction ratio (z / y) were calculated from the obtained weight reduction by the following equation (5).
- Total light transmittance and linear transmittance The total light transmittance and linear transmittance were measured with a double beam type spectrophotometer (manufactured by JASCO Corporation, model V-650). The measurement sample was the same as that used for haze rate measurement. Using a deuterium lamp and a halogen lamp as a light source, the wavelength of 200 nm to 800 nm was scanned, and the linear transmittance at each wavelength was measured. A value at a wavelength of 600 nm was used as a representative value.
- the diffusion coefficient was calculated using equation (3).
- ⁇ ⁇ log (1-H) / d (3) (Average particle size)
- the primary sintered body and the sintered body after the HIP treatment were subjected to surface grinding, and then mirror polished using diamond abrasive grains 9 ⁇ m, 6 ⁇ m, and 1 ⁇ m. After the polished surface was thermally etched, SEM observation was performed.
- the thermal etching was performed by holding for 2 hours at a temperature 50 to 100 ° C. lower than the HIP processing temperature. From the SEM observation of the sintered body after etching, it was found that Am. Ceram. Soc. , 52 [8] 443-6 (1969), the average particle size was determined by the equation (6).
- D 1.56L (6)
- D is an average crystal grain size ( ⁇ m)
- L is an average length ( ⁇ m) of particles crossing an arbitrary straight line
- a value of L is an average value of 100 or more actually measured lengths.
- the bending strength of the zirconia sintered body was measured according to JIS R1601. The measurement was performed 10 times, and the average value was defined as the average bending strength.
- a schlieren image was observed as the refractive index distribution of the zirconia sintered body.
- the schlieren image was observed using a small schlieren apparatus (SLM-10; manufactured by Mizojiri Optical Co., Ltd.).
- Examples 1-7 (Raw material powder) Predetermined amounts of zirconia powder and titania powder were weighed and mixed in a ball mill for 72 hours with a zirconia ⁇ 10 mm ball in an ethanol solvent to prepare a dried powder to obtain a raw material powder.
- zirconia powder 8 mol% yttria-containing zirconia powder (manufactured by Tosoh, TZ-8Y) or 10 mol% yttria-containing zirconia powder (manufactured by Tosoh, TZ-10Y) manufactured by the hydrolysis method is used as the titania powder.
- the molded body was sintered in the atmosphere at a temperature rising rate of 100 ° C./h, a sintering temperature of 1325 ° C. or 1350 ° C., and a sintering time of 2 hours to obtain a primary sintered body (sample number: No. 1 to 4).
- Table 1 shows the composition, density, average particle diameter, and crystal phase of the obtained primary sintered body.
- any of the primary sintered bodies had a relative density of 90% or more, an average particle diameter of 2 ⁇ m or less, and the crystal phase was a mixed phase of cubic and tetragonal crystals.
- HIP processing Sample No.
- the primary sintered bodies of 1, 2, 3, or 4 were subjected to HIP treatment at a predetermined HIP temperature of 1400 ° C. to 1500 ° C., a pressure of 150 MPa, and a holding time of 1 hour.
- Argon gas having a purity of 99.9% was used as the pressure medium.
- a container for installing the sample a carbon container with a lid was used.
- the HIP-treated body after the HIP treatment was all black, and a light-transmitting zirconia sintered body was obtained by annealing at 1000 ° C. for 2 hours in the atmosphere.
- the obtained zirconia sintered body had a density of 100% within the measurement error range of the Archimedes method, and the crystal phase was a fluorite-type cubic single phase.
- Table 2 shows the Ti reduction ratio after the HIP treatment and the characteristics of the zirconia sintered body after the annealing treatment.
- any of the zirconia sintered bodies had a high linear transmittance of 60% or more and a bending strength of 250 MPa or more.
- the sintered body of the present invention was composed of fine crystal particles as shown in FIG.
- Example 8 A schlieren image was observed for the zirconia sintered body of Example 6, and the obtained schlieren image is shown in FIG.
- the zirconia sintered body was a homogeneous sintered body without striae.
- Example 9 The zirconia sintered body of Example 4 was measured for refractive index, Abbe number, relative dielectric constant, dielectric loss, and Vickers hardness.
- the refractive index was measured by a prism coupling method, the relative dielectric constant and dielectric loss were measured in the frequency range of 100 kHz to 1000 kHz, and the Vickers hardness was measured at a load of 5 kg. The results are shown in Table 3.
- Refractive index and relative dielectric constant were extremely high compared to transparent materials such as glass, and dielectric loss was also very small.
- the linear transmittance was less than 1%, and the transmittance was remarkably lowered by the decrease in the HIP processing temperature.
- the crystal phase of the zirconia sintered body of this comparative example was a cubic phase and a tetragonal phase.
- Comparative Example 3 A primary sintered body (sample number: No. 5) was manufactured by using zirconia containing Y 2 O 3 : 9 mol% and TiO 2 : 10 mol% at a temperature of 1500 ° C. and a sintering time of 2 hours. The results of the obtained primary sintered body are shown in Table 5.
- the crystal phase of the obtained primary sintered body was a cubic single phase, and the average particle size was as coarse as 20 ⁇ m or more.
- Example number: No. 5 The obtained primary sintered body (sample number: No. 5) was processed under the same conditions as in Example 1 to produce a zirconia sintered body. The results are shown in Table 6.
- the zirconia sintered body obtained from the cubic sintered body having a crystalline phase has low transmittance after HIP.
- Comparative Example 4 A zirconia sintered body was produced by the same treatment as in Example 4 except that the raw material powder was not mixed.
- the results of the obtained zirconia sintered body are shown in Table 7, and the schlieren image is shown in FIG.
- Examples 10 to 21 Predetermined amounts of zirconia powder and titania powder were weighed, mixed in a ball mill for 72 hours with zirconia ⁇ 10 mm balls in an ethanol solvent, and the dried powder was used as a raw material powder.
- zirconia powder 8 mol% yttria-containing zirconia powder (manufactured by Tosoh, TZ-8Y) or 10 mol% yttria-containing zirconia powder (manufactured by Tosoh, TZ-10Y) produced by the hydrolysis method is used, and sulfuric acid is used as the titania powder.
- the high-purity titania powder produced by the above method Ishihara Sangyo, PT-401M was used.
- the physical properties of the raw material powder are shown in Table 8.
- the raw material powder was molded at a pressure of 50 MPa by a die press, and then further solidified at a pressure of 200 MPa using a cold isostatic press to obtain a cylindrical molded body having a diameter of 20 mm and a thickness of 2 mm.
- a temperature increase rate of 100 ° C./h in the atmosphere, a primary sintering temperature of 1300 ° C. to 1375 ° C. and a sintering time of 2 hours or 10 hours were obtained to obtain a primary sintered body ( Sample number: No. 6 to 13).
- Table 9 shows the composition, density, average particle diameter, and crystal phase of the obtained primary sintered body.
- Each of the primary sintered bodies had a relative density of 94% to 98%, an average particle size of 3 ⁇ m or less, and the crystal phase was a two-phase system of cubic and tetragonal crystals.
- HIP treatment and annealing Sample No. Using the primary sintered body of any one of 6 to 13, HIP treatment was performed at a temperature of 1650 ° C., a pressure of 150 MPa, and a holding time of 1 hour. Argon gas having a purity of 99.9% was used as the pressure medium.
- any one of three types of a carbon container with a lid, a carbon container without a lid, and an alumina container without a lid was used.
- zirconia sintered bodies after the HIP treatment were black, they were annealed in the atmosphere at 1000 ° C. for 2 hours. All the annealed zirconia sintered bodies were colorless and transparent.
- the obtained zirconia sintered body had a density of 100% within the measurement error range of the Archimedes method, and the crystal phase was a fluorite-type cubic single phase.
- Table 10 shows the Ti reduction ratio during the HIP treatment, and the average particle diameter, haze ratio, linear transmittance, diffusion coefficient, brightness, and hue of the zirconia sintered body after annealing.
- the linear transmittance (sample thickness 1 mm and measurement wavelength 600 nm) of any zirconia sintered body is 73% to 74%, the haze ratio is very low, 0.3% to 1.0%, and high without turbidity. It had transparency.
- Examples 22-25 Preparation of raw material powder 8 mol% yttria-containing zirconia powder (manufactured by Tosoh, TZ-8Y) and titania powder (manufactured by Showa Denko, super titania) manufactured by a gas phase method are mixed in a ball mill to produce 7.2 mol% yttria and 10 mol% titania-containing zirconia powder.
- 8 mol% yttria-containing zirconia powder manufactured by Tosoh, TZ-8Y
- titania powder manufactured by Showa Denko, super titania
- Table 11 shows the physical properties of the titania powder used.
- a primary sintered body was obtained by molding and primary firing in the same manner as in Examples 19 to 21 except that primary sintering was held in air at 1325 ° C. for 2 hours (sample number: No. 14).
- HIP treatment and annealing A zirconia sintered body was obtained in the same manner as in Examples 19 to 21, except that the HIP treatment temperature was changed to 1600 ° C or 1700 ° C. The characteristics of the zirconia sintered body are shown in Table 12.
- Example 26 A zirconia sintered body containing yttria 7.2 mol% and titania 10 mol% was produced in the same manner as in Example 12. The refractive index, Abbe number, relative dielectric constant, 3-point bending strength, and Vickers hardness were measured. The results are shown in Table 13.
- the refractive index was measured by the prism coupling method, the relative dielectric constant was measured in the frequency range of 100 kHz to 1000 kHz, the three-point bending strength was measured based on JIS R1601, and the Vickers hardness was measured at a load of 5 kg.
- Refractive index and relative dielectric constant were extremely high compared to transparent materials such as glass, and excellent mechanical properties.
- the zirconia sintered body obtained from any primary sintered body has a low Ti reduction ratio.
- the sintered body obtained from No. 7 was 3%, sample No.
- the sintered body obtained from 10 was 5%.
- the linear transmittance of the sintered body is the sample No.
- the sintered body obtained from No. 7 was 45%, sample No.
- the sintered body obtained from 10 was 64%.
- the haze ratio is the sample number no. 29% of the sintered body obtained from No. 7, sample number No.
- the sintered body obtained from 10 was 11%. In both cases, the haze ratio is 10% or more and the linear transmittance is 65% or less, the transparency is low, and Sample No.
- the diffusion coefficient of the sintered body obtained from No. 10 was as high as 1.03 cm ⁇ 1 .
- Comparative Example 6 A primary sintered body using the molded body made of the raw material powder (9.0 mol% yttria and Y 2 O 3 10 mol% titania) used in Examples 16 to 19 and holding at 1500 ° C. and 1600 ° C. for 2 hours. Got. The average grain size of the primary sintered body was 15.0 ⁇ m of the primary sintered body (sample number: No. 15) sintered at 1500 ° C. (sample number: No. 16). ) was 30.3 ⁇ m.
- the obtained primary sintered body was subjected to HIP treatment in the same manner as in Example 18 to obtain a zirconia sintered body.
- the linear transmittance is the sample number No.
- the zirconia sintered body obtained from No. 15 was 55%
- the zirconia sintered body obtained from No. 16 was 48%
- the haze ratio was Sample No. No. 15 is 20% of the zirconia sintered body obtained from Sample No.
- the zirconia sintered body obtained from No. 16 was 27%, both of which had poor transparency.
- Example 27 and Comparative Example 7 With respect to 9.0 mol% yttria and 10 mol% titania-containing zirconia, changes in the primary sintered body structure due to the sintering temperature were observed. The figure which shows the result of SEM observation was shown to FIG. 5A, 5B, and 5C.
- the primary sintered body (sample number: No. 10) held at 1300 ° C. for 10 hours and the primary sintered body held at 1400 ° C. for 2 hours, all the pores are present at the grain boundaries, but at 1500 ° C.
- the primary sintered body (sample number: No. 15) held for 2 hours, a large number of pores incorporated in the grains were present.
- Example 28 Based on the data of Examples 10 to 25 and Comparative Example 5, the relationship between the Ti reduction ratio and the haze ratio was determined. The results are shown in FIG.
- Example 29 Based on the data of Examples 10 to 25 and Comparative Example 6, the relationship between the primary sintering temperature and the haze ratio was determined. The results are shown in FIG.
- Comparative Example 8 According to Patent Document 2, a zirconia sintered body was obtained. According to Patent Document 2 Powder Production Examples 8 to 13, 7 mol% yttria and 10 mol% titania-containing zirconia powder was obtained, and sintered according to Sintering Example A at 1700 ° C. in an oxygen flow and then subjected to HIP treatment at 1500 ° C. and 100 MPa. The Ti reduction ratio after the HIP treatment was 18%.
- the obtained zirconia sintered body had a linear transmittance of 65% and a haze ratio of 9%, which was lower in transparency than the zirconia sintered body of the present invention.
- Patent Document 1 According to the method described in Patent Document 1, a zirconia sintered body was obtained.
- Patent Document 1 According to Example 1, using 8 mol% yttria-containing zirconia powder (manufactured by Tosoh Corporation, TZ-8Y), primary sintering was performed at 1375 ° C., and HIP treatment was performed at 1750 ° C. and 150 MPa in a semi-sealed alumina container. .
- the obtained sintered body had a linear transmittance of 72.5%, a haze ratio of 2.5%, and a diffusion coefficient of 0.251 cm ⁇ 1 and was turbid (cloudy).
- the zirconia sintered body of the present invention is excellent in high translucency and mechanical strength, it can be used as a decorative product.
- electronic parts such as watch parts, decorative members, transparent panels for mobile phones and electronic devices, etc. It can be used as equipment exterior parts, aesthetic dental parts, and the like.
- the zirconia sintered bodies of the present invention in the case of a sintered body having a particularly high translucency, when used as an optical lens or an optical prism, a high refraction with a refractive index of 2.0 or higher that cannot be achieved with glass. You can do things of rate. Furthermore, since it is excellent in mechanical properties, it can also be used as a decorative part. For example, it can be used as an exterior part for electronic devices such as watches and mobile phones.
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Abstract
Description
(1)イットリアを6mol%~15mol%とチタニアを3mol%~20mol%含有し、試料厚さ1mmで測定波長600nmにおいて直線透過率が50%以上であることを特徴とするジルコニア焼結体。
(2)好ましくは、平均粒径が30μm未満であることを特徴とする上記(1)に記載のジルコニア焼結体。
(3)好ましくは、平均曲げ強度が250MPa以上であることを特徴とする上記(2)に記載のジルコニア焼結体。
(4)好ましくは、焼結密度が99.9%以上であることを特徴とする上記(2)に記載のジルコニア焼結体。
(5)好ましくは、結晶相が立方晶蛍石構造であることを特徴とする上記(2)に記載のジルコニア焼結体。
(6)好ましくは、試料厚さ1mmで測定波長600nmにおいて、直線透過率が73%以上であり、かつ、ヘーズ率2.0%以下の上記(1)に記載のジルコニア焼結体。
(7)好ましくは、平均結晶粒径が30μm以上60μm以下であることを特徴とする上記(1)に記載のジルコニア焼結体。
(8)好ましくは、明度L*が84以上90以下であることを特徴とする上記(7)に記載のジルコニア焼結体。
(9)好ましくは、色相が、a*が-1.5以上0.2以下、かつ、b*が0.0以上4.0以下であることを特徴とする上記(7)に記載のジルコニア焼結体。
(10)3mol%~20mol%のチタニアと6mol%~15mol%のイットリアを含有するジルコニア粉末を成形後、常圧で一次焼結し、熱間静水圧プレス(HIP)処理してTi還元比率20%以上の焼結体を得、該焼結体をアニール処理することを特徴とする3mol%~20mol%のチタニアと6mol%~15mol%のイットリアを含有するジルコニア焼結体の製造方法。
(11)好ましくは、相対密度94%以上及び平均粒径3μm以下の一次焼結体をHIP処理することを特徴とする上記(10)に記載のジルコニア焼結体の製造方法。
(12)好ましくは、1200℃~1400℃で焼結した焼結体をHIP処理することを特徴とする上記(10)に記載のジルコニア焼結体の製造方法。
(13)好ましくは、HIP処理を1400℃以上1800℃以下で行うことを特徴とする上記(10)に記載のジルコニア焼結体の製造方法。
(14)上記(1)に記載のジルコニア焼結体を用いた光学部品。
(15)好ましくは、光学用レンズに用いる上記(14)の光学部品。
(16)上記(1)に記載のジルコニア焼結体を用いる電子機器用外装部品。
Tt:全光線透過率(%)
Td:拡散透過率(%)
Ti:直線透過率(%)
特に高い透光性を有するジルコニアの場合は、試料厚さ1mmでヘーズ率2.0%以下であることが好ましく、1.0%以下であることがより好ましい。ヘーズ率が2.0%を越えると焼結体に曇りが多くなり、光学材料用途へは用いることができにくい。一方、ヘーズ率は小さい程好ましいが、2.0%以下であれば光学材料用途に用いるのに十分な透明性となる。
H :ヘーズ率(%)
Tt:全光線透過率(%)
Td:拡散透過率(%)
本発明のジルコニア焼結体は脈理が無いことが好ましい。脈理が発生すると、屈折率差による光散乱のため透光性が低下しやすい。
κ=-log(Ti/Tt)/d (3)’
κ:拡散係数(cm-1)
H:ヘーズ率(%)
Ti:直線透過率(%)
Tt:全光線透過率(%)
d:試料厚み(cm)
拡散係数はヘーズ率が高いほど増加し、例えば、ヘーズ率が2.0%以下であれば、測定波長600nmにおいて(3)式により求まる拡散係数は0.15cm-1以下となる。
酸素空孔の形成により結晶格子内での物質移動が容易になるため、残留気孔の移動(消滅)が促進される。
HIP処理後とアニール後の焼結体の重量変化を測定し、得られた重量減少から下記(5)式によって、Ti3+含量(z)、Ti還元比率(z/y)を算出した。
(全光線透過率及び直線透過率)
全光線透過率及び直線透過率はダブルビーム方式の分光光度計(日本分光株式会社製、V-650型)で測定した。測定試料はヘーズ率測定に用いたのと同様のものとした。重水素ランプ及びハロゲンランプを光源として波長200nm~800nmをスキャンして各波長での直線透過率を測定した。600nmの波長での値を代表値とした。
ジルコニア焼結体を、厚み1mmに加工し、表面粗さRa=0.02μm以下に両面鏡面研磨したものを測定試料として用いた。ヘーズ率はJIS K7105「プラスチックの光学的特性試験方法」、JIS K7136「プラスチック-透明材料のヘーズの求め方」に準じた方法で、ヘーズメーター(東京電色製、TC-HIII)を用いて測定した。
(平均粒径)
一次焼結体及びHIP処理後の焼結体を平面研削した後、ダイアモンド砥粒9μm、6μm、及び1μmを用いて鏡面研磨した。研磨面を熱エッチングした後、SEM観察した。
ここで、Dは平均結晶粒径(μm)、Lは任意の直線を横切る粒子の平均長さ(μm)であり、Lの値は100本以上の実測長さの平均値とした。
測定試料として試料厚みを1mmに加工し、表面粗さRa=0.02μm以下に両面鏡面研磨したものを用いた。測定はJIS K7105「プラスチックの光学的特性試験方法」の5.3項、5.4項に準じて、精密型分光光度色彩計(東京電色製、TC-1500SX)を用いて行った。試料の裏面に常用標準白色板を置き、試料からの反射光を測定して、明度L*、色相a*及びb*を求めた。
ジルコニア焼結体の曲げ強度はJIS R1601に従い測定した。測定は10回行い、その平均値を平均曲げ強度とした。
ジルコニア焼結体の屈折率分布としてシュリーレン像を観察した。シュリーレン像は、小型シュリーレン装置(SLM-10;、溝尻光学工業所製)を用いて観察した。
(原料粉末)
ジルコニア粉末及びチタニア粉末を所定量秤量し、エタノール溶媒中ジルコニア製φ10mmボールで72時間ボールミル混合し、乾燥した粉末を調製して原料粉末とした。
原料粉末を金型プレスによって圧力50MPaで成形した後、冷間静水圧プレス装置を用い圧力200MPaで更に固め、直径20mmの円柱成形体を得た。
(HIP処理)
試料番号No.1、2、3、又は4の一次焼結体を1400℃~1500℃の所定のHIP温度、圧力150MPa、保持時間1時間でHIP処理した。なお、圧力媒体として純度99.9%のアルゴンガスを用いた。試料を設置する容器としては、蓋付きカーボン製容器を用いた。
いずれのジルコニア焼結体も直線透過率は60%以上と高く、かつ、曲げ強度も250MPa以上と高いものであった。本発明の焼結体は、図1に示したように微細な結晶粒子から構成されていた。
実施例6のジルコニア焼結体についてシュリーレン像を観察し、得られたシュリーレン像を図3に示した。ジルコニア焼結体は脈理の無い均質な焼結体であった。
実施例4のジルコニア焼結体について屈折率、アッベ数、比誘電率、誘電損失、及びビッカース硬度を測定した。屈折率はプリズムカップリング法で、比誘電率及び誘電損失は周波数100kHz~1000kHzの範囲で、ビッカース硬度は荷重5kgでそれぞれ測定した。結果を表3に示した。
Y2O3:9mol%、TiO2:10mol%を含むジルコニアを、温度1500℃、焼結時間2時間として一次焼結体(試料番号:No.5)を製造した。得られた一次焼結体の結果を表5に示した。
原料粉末の混合を行わなかった以外は、実施例4と同様な処理によりジルコニア焼結体を製造した。得られたジルコニア焼結体の結果を表7に、シュリーレン像を図4に示した。
(HIP処理及びアニール)
試料番号No.6~13のいずれかの一次焼結体を用い、温度1650℃、圧力150MPa、及び保持時間1時間でHIP処理した。なお、圧力媒体として純度99.9%のアルゴンガスを用いた。
(原料粉末の調製)
8mol%イットリア含有ジルコニア粉末(東ソー製、TZ-8Y)と気相法で製造されたチタニア粉末(昭和電工製、スーパーチタニア)をボールミル混合して、7.2mol%イットリア及び10mol%チタニア含有ジルコニア粉末を得た。
(一次焼結)
一次焼結を大気中、1325℃で、2h保持した以外は、実施例19~21と同様に成型、一次焼成して一次焼結体を得た(試料番号:No.14)。
(HIP処理及びアニール)
HIP処理温度を1600℃もしくは1700℃に変えた以外は、実施例19~21と同様の方法でジルコニア焼結体を得た。ジルコニア焼結体の特性を表12に示した。
実施例26
実施例12と同様の方法でイットリア7.2mol%及びチタニア10mol%を含有するジルコニア焼結体を作製した。それについて、屈折率、アッベ数、比誘電率、3点曲げ強度、及びビッカース硬度を測定した。結果を表13に示した。
比較例5
試料番号No.7(7.2mol%イットリア及び10mol%チタニア)、並びに試料番号No.10(9.0mol%イットリア及び10mol%チタニア)の一次焼結体を用い、それを蓋付きアルミナ容器に設置した以外は実施例11と全く同様の方法でHIP処理してジルコニア焼結体を得た。
実施例16~19で用いた原料粉末(9.0mol%イットリア及びY2O310mol%チタニア)からなる成形体を用い、1500℃及び1600℃の各温度で2時間保持して一次焼結体を得た。一次焼結体の平均粒径は、1500℃で焼結した一次焼結体(試料番号:No.15)が15.0μm、1600℃で焼結した一次焼結体(試料番号:No.16)が30.3μmであった。
9.0mol%イットリア及び10mol%チタニア含有ジルコニアについて、焼結温度による一次焼結体組織の変化を観察した。SEM観察の結果を示す図を図5A、5B及び5Cに示した。1300℃で、10h保持した一次焼結体(試料番号:No.10)、及び1400℃で、2時間保持した一次焼結体では、気孔はすべて粒界に存在しているが、1500℃で、2時間保持した一次焼結体(試料番号:No.15)では、粒内に取り込まれた気孔が多数存在していた。又、各試料の結晶相をXRDで同定した結果、1300℃又は1400℃で焼結した一次焼結体(実施例27)には立方晶の他に正方晶が認められたが、1500℃で焼結した一次焼結体(比較例7)には立方晶のみ認められた。
実施例10~25、及び比較例5のデータをもとにTi還元比率とヘーズ率との関係を求めた。結果を図6に示した。
実施例10~25、及び比較例6のデータをもとに一次焼結温度とヘーズ率との関係を求めた。結果を図7に示した。
特許文献2に従って、ジルコニア焼結体を得た。特許文献2粉末製造例8~13に従って、7mol%イットリア及び10mol%チタニア含有ジルコニア粉末を得、焼結例Aに従って、酸素流通中1700℃で焼結後、1500℃及び100MPaでHIP処理した。HIP処理後のTi還元比率は18%であった。
特許文献1に記載された方法に従ってジルコニア焼結体を得た。特許文献1実施例1に従って、8mol%イットリア含有ジルコニア粉末(東ソー製、TZ-8Y)を用い、一次焼結を1375℃で行い、HIP処理を半密閉アルミナ容器中で1750℃及び150MPaで行った。得られた焼結体は、直線透過率72.5%、ヘーズ率2.5%、及び拡散係数0.251cm-1であり、濁り(曇り)があるものであった。
Claims (16)
- イットリアを6mol%~15mol%とチタニアを3mol%~20mol%含有し、試料厚さ1mmで測定波長600nmにおいて直線透過率が50%以上であることを特徴とするジルコニア焼結体。
- 平均粒径が30μm未満であることを特徴とする請求項1に記載のジルコニア焼結体。
- 平均曲げ強度が250MPa以上であることを特徴とする請求項2に記載のジルコニア焼結体。
- 焼結密度が99.9%以上であることを特徴とする請求項2に記載のジルコニア焼結体。
- 結晶相が立方晶蛍石構造であることを特徴とする請求項2に記載のジルコニア焼結体。
- 試料厚さ1mmで測定波長600nmにおいて、直線透過率が73%以上であり、かつ、ヘーズ率2.0%以下の請求項1に記載のジルコニア焼結体。
- 平均結晶粒径が30μm以上60μm以下であることを特徴とする請求項6に記載のジルコニア焼結体。
- 明度L*が84以上90以下であることを特徴とする請求項7に記載のジルコニア焼結体。
- 色相が、a*が-1.5以上0.2以下、かつ、b*が0.0以上4.0以下であることを特徴とする請求項7に記載のジルコニア焼結体。
- 3mol%~20mol%のチタニアと6mol%~15mol%のイットリアを含有するジルコニア粉末を成形後、常圧で一次焼結し、熱間静水圧プレス(HIP)処理してTi還元比率20%以上の焼結体を得、該焼結体をアニール処理することを特徴とする3mol%~20mol%のチタニアと6mol%~15mol%のイットリアを含有するジルコニア焼結体の製造方法。
- 相対密度94%以上及び平均粒径3μm以下の一次焼結体をHIP処理することを特徴とする請求項10に記載のジルコニア焼結体の製造方法。
- 1200℃~1400℃で焼結した焼結体をHIP処理することを特徴とする請求項10に記載のジルコニア焼結体の製造方法。
- HIP処理を1400℃以上1800℃以下で行うことを特徴とする請求項10に記載のジルコニア焼結体の製造方法。
- 請求項1に記載のジルコニア焼結体を用いた光学部品。
- 光学用レンズに用いる請求項14の光学部品。
- 請求項1に記載のジルコニア焼結体を用いる電子機器用外装部品。
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US13/320,441 US8722555B2 (en) | 2009-06-04 | 2010-06-03 | High-strength transparent zirconia sintered body, process for producing the same, and uses thereof |
EP21153959.8A EP3831797B1 (en) | 2009-06-04 | 2010-06-03 | High-strength transparent zirconia sintered body, process for producing the same, and uses thereof |
CN2010800244542A CN102803180A (zh) | 2009-06-04 | 2010-06-03 | 高强度透明氧化锆烧结体、其制造方法及其用途 |
US14/168,651 US9249058B2 (en) | 2009-06-04 | 2014-01-30 | High-strength transparent zirconia sintered body, process for producing the same, and uses thereof |
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US14/168,651 Continuation US9249058B2 (en) | 2009-06-04 | 2014-01-30 | High-strength transparent zirconia sintered body, process for producing the same, and uses thereof |
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Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011102227A (ja) * | 2009-10-16 | 2011-05-26 | Tosoh Corp | 高強度透明ジルコニア焼結体 |
JP2014218398A (ja) * | 2013-05-08 | 2014-11-20 | 信越化学工業株式会社 | 透光性金属酸化物焼結体の製造方法及び透光性金属酸化物焼結体 |
US20150283791A1 (en) * | 2012-12-07 | 2015-10-08 | Tosoh Corporation | Composite plate and method for producing same |
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EP3831797B1 (en) | 2009-06-04 | 2023-05-10 | Tosoh Corporation | High-strength transparent zirconia sintered body, process for producing the same, and uses thereof |
WO2011016325A1 (ja) | 2009-08-07 | 2011-02-10 | 東ソー株式会社 | 透明ジルコニア焼結体及びその製造方法、並びにその用途 |
WO2012063746A1 (ja) * | 2010-11-11 | 2012-05-18 | 東ソー株式会社 | 着色透光性ジルコニア焼結体及びその製造方法並びにその用途 |
EP3088374B1 (en) | 2010-12-20 | 2018-09-05 | Tosoh Corporation | Gallium nitride molded article and method for producing same |
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KR20130142000A (ko) * | 2012-06-18 | 2013-12-27 | 삼성전자주식회사 | 이미지 센서, 이를 포함하는 이미지 처리 장치, 및 이의 제조 방법 |
DE102012022237A1 (de) * | 2012-11-14 | 2014-05-15 | Heraeus Materials Technology Gmbh & Co. Kg | Sputtertarget mit optimierten Gebrauchseigenschaften |
WO2014142080A1 (ja) * | 2013-03-11 | 2014-09-18 | クラレノリタケデンタル株式会社 | ジルコニア焼結体、並びにジルコニアの組成物及び仮焼体 |
KR102215498B1 (ko) | 2013-06-27 | 2021-02-15 | 이보클라 비바덴트 인코퍼레이티드 | 나노결정질 지르코니아 및 그의 가공 방법 |
US9520303B2 (en) | 2013-11-12 | 2016-12-13 | Applied Materials, Inc. | Aluminum selective etch |
EP2889279B1 (en) * | 2013-12-27 | 2022-08-24 | Vatechacucera, Inc. | Machinable Zirconia |
KR101846488B1 (ko) | 2014-08-07 | 2018-04-09 | 주식회사 페코텍 | 상이한 결정상을 포함하는 지르코니아-이트리아-지르코늄 실리케이트 소결체 |
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US9822039B1 (en) | 2016-08-18 | 2017-11-21 | Ivoclar Vivadent Ag | Metal oxide ceramic nanomaterials and methods of making and using same |
DE102018103906A1 (de) | 2017-02-22 | 2018-08-23 | James R. Glidewell Dental Ceramics, Inc. | Hochfeste und transluzente Dentalkeramikmaterialien, -einrichtungen und -verfahren |
US11161789B2 (en) | 2018-08-22 | 2021-11-02 | James R. Glidewell Dental Ceramics, Inc. | Highly translucent zirconia material, device, methods of making the same, and use thereof |
EP3659548A1 (de) * | 2018-11-29 | 2020-06-03 | Ivoclar Vivadent AG | Verfahren zur herstellung einer dentalen restauration |
EP3950638A4 (en) * | 2019-03-26 | 2022-12-21 | Tosoh Corporation | ZIRCONIA SINTERED BODY AND METHOD OF MANUFACTURE THEREOF |
EP4003938A4 (en) * | 2019-07-26 | 2023-08-30 | The Regents of The University of California | ULTRA-RAPID LASER WELDING OF CERAMICS |
CN110357621B (zh) * | 2019-08-12 | 2022-05-17 | Oppo广东移动通信有限公司 | 陶瓷壳体及其制备方法、电子设备 |
US11672632B2 (en) | 2020-10-05 | 2023-06-13 | Pritidenta Gmbh | Multi-layered zirconia dental blank with reverse layers, process for its preparation and uses thereof |
CN114751740B (zh) * | 2022-04-28 | 2023-03-28 | 中国科学院上海硅酸盐研究所 | 大尺寸高透明钇稳定氧化锆陶瓷及其制备方法 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6291467A (ja) * | 1985-06-20 | 1987-04-25 | 東ソー株式会社 | 透光性ジルコニア焼結体の製造法 |
JP2008222450A (ja) * | 2007-03-08 | 2008-09-25 | Tosoh Corp | 透光性イットリア含有ジルコニア焼結体及びその製造方法並びにその用途 |
Family Cites Families (16)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4758541A (en) * | 1985-06-20 | 1988-07-19 | Toyo Soda Manufacturing Co., Ltd. | Zirconia sintered body of improved light transmittance |
US4753902A (en) * | 1986-11-24 | 1988-06-28 | Corning Glass Works | Transformation toughened zirconia-titania-yttria ceramic alloys |
JPH01113038A (ja) | 1987-07-02 | 1989-05-01 | Tosoh Corp | 歯列矯正ブラケット |
JP2569622B2 (ja) | 1987-11-11 | 1997-01-08 | 東ソー株式会社 | 透光性ジルコニア質焼結体の製造方法 |
JP2569662B2 (ja) * | 1987-12-28 | 1997-01-08 | 東ソー株式会社 | 透光性ジルコニア質焼結体の製造方法 |
JP2762508B2 (ja) | 1989-01-30 | 1998-06-04 | 東ソー株式会社 | ジルコニア焼結体およびその製造法 |
JPH03150263A (ja) | 1989-11-02 | 1991-06-26 | Jgc Corp | 黒色ジルコニアセラミックスおよびその製造方法 |
JP2569662Y2 (ja) | 1991-10-02 | 1998-04-28 | フジコピアン株式会社 | 塗膜転写テープの走行構造 |
US20050165835A1 (en) | 2001-06-14 | 2005-07-28 | Sharp Kabushiki Kaisha | Data processing method, program and data processing apparatus |
JP4470378B2 (ja) | 2003-02-28 | 2010-06-02 | 住友化学株式会社 | ジルコニア焼結体およびその製造方法 |
JP2007108734A (ja) | 2005-09-21 | 2007-04-26 | Schott Ag | 光学素子及び同光学素子から成る撮像光学素子 |
JP5125065B2 (ja) | 2006-02-17 | 2013-01-23 | 東ソー株式会社 | 透明ジルコニア焼結体 |
WO2008013099A1 (fr) | 2006-07-25 | 2008-01-31 | Tosoh Corporation | Zircone frittée ayant une transmission de lumière élevée et une résistance élevée, son utilisation et son procédé de fabrication |
JP4946939B2 (ja) | 2008-03-27 | 2012-06-06 | 双葉電子工業株式会社 | 相関器及び超広帯域無線受信装置 |
JP5325518B2 (ja) | 2008-07-22 | 2013-10-23 | ショット アクチエンゲゼルシャフト | 透明セラミック及びその製造方法ならびにその透明セラミックスを用いた光学素子 |
EP3831797B1 (en) | 2009-06-04 | 2023-05-10 | Tosoh Corporation | High-strength transparent zirconia sintered body, process for producing the same, and uses thereof |
-
2010
- 2010-06-03 EP EP21153959.8A patent/EP3831797B1/en active Active
- 2010-06-03 EP EP10783426.9A patent/EP2439182B1/en active Active
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- 2014-01-30 US US14/168,651 patent/US9249058B2/en active Active
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS6291467A (ja) * | 1985-06-20 | 1987-04-25 | 東ソー株式会社 | 透光性ジルコニア焼結体の製造法 |
JP2008222450A (ja) * | 2007-03-08 | 2008-09-25 | Tosoh Corp | 透光性イットリア含有ジルコニア焼結体及びその製造方法並びにその用途 |
Non-Patent Citations (1)
Title |
---|
See also references of EP2439182A4 * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011102227A (ja) * | 2009-10-16 | 2011-05-26 | Tosoh Corp | 高強度透明ジルコニア焼結体 |
US20150283791A1 (en) * | 2012-12-07 | 2015-10-08 | Tosoh Corporation | Composite plate and method for producing same |
US10682831B2 (en) * | 2012-12-07 | 2020-06-16 | Tosoh Corporation | Composite plate and method for producing same |
JP2014218398A (ja) * | 2013-05-08 | 2014-11-20 | 信越化学工業株式会社 | 透光性金属酸化物焼結体の製造方法及び透光性金属酸化物焼結体 |
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EP2439182A1 (en) | 2012-04-11 |
KR20120030401A (ko) | 2012-03-28 |
US9249058B2 (en) | 2016-02-02 |
EP3831797B1 (en) | 2023-05-10 |
EP2439182B1 (en) | 2021-03-17 |
KR101699525B1 (ko) | 2017-01-24 |
US20120058883A1 (en) | 2012-03-08 |
CN102803180A (zh) | 2012-11-28 |
US20140145125A1 (en) | 2014-05-29 |
US8722555B2 (en) | 2014-05-13 |
EP3831797A1 (en) | 2021-06-09 |
EP2439182A4 (en) | 2013-07-17 |
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