JP2018030775A - Zirconia sintered body, zirconia composition and zirconia calcined body, and prosthesis for dentistry - Google Patents

Abstract

PROBLEM TO BE SOLVED: To provide a zirconia sintered body which suppresses distorted shrinkage deformation.SOLUTION: A plurality of zirconia powder which contains zirconia and a stabilizer and has different compositions is formed and laminated to form a zirconia composition, which is fired at 800°C-1,200°C to produce a zirconia calcined body 20. The zirconia calcined body 20 is molded into a rectangular parallelepiped having a width of 50 mm, a height of 10 mm and a depth of 5 mm to prepare a test piece. In the test piece, when the surface of a width of 50 mm and a depth of 5 mm is a bottom face, a boundary surface formed by laminating the zirconia powder is parallel to the bottoms surface. The test piece is fired at 1,500°C for two hours, and a bottom face 20a of two bottom faces that is deformed in a concave surface is set downward. The zirconia calcined body, in which a ratio of (maximum space between concave bottom face and contact surface) d/(distance between contact parts in width direction) L×100 is 0.15 or less, is fired at 1,400-1,600°C to obtain a zirconia sintered body.SELECTED DRAWING: Figure 3

Description

  The present invention relates to a zirconia calcined body. The present invention also relates to a composition for producing a zirconia calcined body. The present invention relates to a zirconia sintered body produced from a zirconia calcined body. Furthermore, this invention relates to the dental prosthesis (prosthetic material) which has a zirconia sintered compact.

Ceramics such as a sintered body of zirconium oxide (IV) (ZrO ₂ ) (hereinafter referred to as “zirconia”) are used in various fields. For example, zirconia sintered bodies having high strength are applied to dental prosthetic materials, tools, and the like.

  Such ceramics are manufactured by sintering a compact of a raw material powder or a calcined body thereof. In the sintering process, the molded body and the calcined body shrink. Therefore, the dimensions of the compact or calcined body and the dimensions of the sintered body are different. Then, the method of relieving the influence by baking shrinkage is disclosed (for example, refer patent documents 1-3).

  Patent Document 1 discloses a method for producing a ceramic sintered body in which a starting material is mixed with a stabilizer, a sintering aid, and the like, and a material added with a binder is molded and fired. Obtain the relationship between the average particle size and the shrinkage rate during firing, prepare molds with different dimensions according to each shrinkage rate, and determine the average particle size of the mixed raw material before adding the binder during the main molding. A method of manufacturing a ceramic sintered body that is measured, molded using a molding die corresponding to the shrinkage ratio obtained from the average particle diameter, and fired is disclosed.

  In Patent Document 2, a part of the pre-molding raw material is taken out and molded in a ceramic sintered body obtained by molding and sintering a pre-molding raw material in which a stabilizer, a sintering aid, etc. are added to a starting raw material and a binder is added. Then, after measuring the dimension of the specific part of the ceramic molded body or the dimension of the specific part of the molding die, drying or firing, and again measuring the dimension of the specific part of the ceramic dried body or ceramic sintered body, After performing a preliminary test to calculate the shrinkage rate, select a molding die based on the shrinkage rate calculated above so that a specific part of the ceramic sintered body has a desired size, and perform main molding and main firing. A method for manufacturing a ceramic sintered body is disclosed.

  In Patent Document 3, there is a dimension-fidelity sintering method for a ceramic molded object, in which a fired product is supported on a non-metal-coated support material during sintering, and the support material is generated during the firing process. Disclosed is a method for size-fidelity sintering of ceramic molding objects that automatically adapts to shrinkage or allows the molding objects to be supported without contact.

  When a zirconia sintered body is used for an artificial tooth as a substitute for a natural tooth, the artificial tooth is required to have the same appearance as the natural tooth. As a technique for adjusting the appearance of an artificial tooth, Patent Document 4 discloses a multi-colored molded article having layers arranged on top of each other in order to manufacture a dental restoration. The molded body described in Patent Document 4 includes at least two of (a) at least two continuous and different color main layers, and (b) the at least two continuous and different color main layers. With different color intermediate layers, where the change in color between these intermediate layers occurs in a direction opposite to the direction of change in color between the main layers.

JP 2003-137651 A JP 2003-73164 A Special Table 2002-536279 Publication JP 2008-68079 A

  The following analysis is given from the perspective of the present invention.

  Some types of products to which the zirconia sintered body is applied require high dimensional accuracy. For example, in the case of an artificial tooth used for dental treatment, the artificial tooth cannot be applied to the patient unless the shape and size of the artificial tooth and the size and shape of the patient's abutment tooth collected in advance are matched.

  If the sintered body is different from the planned shape / dimension, it may be possible to adjust it to the desired shape / dimension by machining such as cutting / grinding, but since the zirconia sintered body has high strength, It is not easy, and it is necessary to remanufacture, especially when the adjustment amount is large. In this case, production time and product cost increase.

  The methods described in Patent Documents 1 to 3 require labor and new manufacturing equipment, and even if a sintered body having a desired size is obtained, an increase in manufacturing time and manufacturing cost is inevitable. In particular, when an artificial tooth is manufactured, since the artificial tooth is a one-point object, as in Patent Documents 1 and 2, when a mold for it is manufactured, the product cost becomes very high.

  Further, in the heat treatment or sintering of a molded body having a laminated structure as described in Patent Document 4, peeling between layers or distorted shrinkage deformation may occur. Such peeling and deformation cannot be prevented by the methods described in Patent Documents 1 to 3.

  According to the first aspect of the present invention, a zirconia composition containing a stabilizer that suppresses phase transition of zirconia and zirconia is formed by forming a plurality of zirconia powders having different compositions, and laminating a plurality of zirconia powders. And the zirconia calcined body manufactured by baking a zirconia composition at 800 to 1200 degreeC is provided. When the calcined body is molded into a rectangular parallelepiped shape with dimensions of 50 mm width × 10 mm height × 5 mm depth, the test piece has a bottom surface that is 50 mm wide × 5 mm depth by stacking zirconia powder. The formed boundary surface is parallel to the bottom surface, and when the test piece was baked at 1500 ° C. for 2 hours and placed with the bottom surface of the two bottom surfaces deformed into the concave surface (deformed into the concave surface) The maximum distance between the bottom surface and the ground contact surface / (distance between ground contact portions in the width direction) × 100 is 0.15 or less.

  According to the 2nd viewpoint of this invention, the zirconia sintered compact manufactured by the method including the process of sintering the zirconia calcined body of this invention at 1400 degreeC-1600 degreeC is provided.

  According to the 3rd viewpoint of this invention, the zirconia composition used as the calcined body of this invention by baking at 800 to 1200 degreeC is provided.

  According to the 4th viewpoint of this invention, the zirconia composition used as the zirconia sintered compact of this invention by sintering at 1400 degreeC-1600 degreeC is provided.

  According to the fifth aspect of the present invention, there is provided a dental prosthesis that is sintered after the calcined body of the present invention is cut. The dental prosthesis is in a state where it is sintered after cutting the calcined body according to the first viewpoint.

  The present invention has at least one of the following effects.

  According to the zirconia calcined body of the present invention, a zirconia sintered body with high dimensional accuracy can be obtained even when a zirconia calcined body is manufactured by laminating zirconia powders having different compositions.

The schematic diagram of the test piece for measuring the deformation amount at the time of sintering. The schematic diagram of the test piece for measuring the deformation amount at the time of sintering. The schematic diagram for demonstrating the measuring method of deformation. The schematic diagram for demonstrating a three-point bending test method. The schematic diagram of a zirconia sintered compact. The schematic diagram and measurement result of the test piece in Example 5. FIG. The schematic diagram of a test piece in comparative example 3, and a measurement result.

  The preferable form of each said viewpoint is described below.

  According to a preferred embodiment of the first aspect, (the maximum distance between the bottom surface deformed into a concave surface and the ground contact surface) / (the distance between the ground contact portions in the width direction) × 100 is 0.1 or less.

  According to the preferred form of the first aspect, the plurality of zirconia powders contain pigments, and the pigment content is different.

According to the preferable form of the second viewpoint, the L ^* a ^* b ^* table of the first point in the section extending from one end to 25% of the total length on a straight line extending from the one end to the other end in the first direction. The chromaticity (L ^* , a ^* , b ^* ) by the color system is (L1, a1, b1), and the L ^* a ^* b ^* color system of the second point in the section from the other end to 25% of the total length. When the chromaticity (L ^* , a ^* , b ^* ) by (1) is (L2, a2, b2), L1 is 58.0 or more and 76.0 or less, and a1 is -1.6 or more and 7.6 or less. B1 is 5.5 to 26.7, L2 is 71.8 to 84.2, a2 is −2.1 to 1.8, and b2 is 1.9 to 16. is less than or equal to 0, <is L2, a1> L1 is a2, a b1> b2, from a first point towards the second point ^L * ^a * ^{b *} It does not change tendency of increase or decrease the chromaticity due to color system.

According to the preferred form of the second viewpoint, there is no section in which the L ^* value decreases by 1 or more from the first point toward the second point on the straight line connecting the first point and the second point. There is no section where the a ^* value increases by 1 or more from one point toward the second point, and there is no section where the b ^* value increases by one or more from the first point toward the second point.

According to the preferred form of the second viewpoint, on the straight line connecting the first point to the second point, the color by the L ^* a ^* b ^* color system of the third point between the first point and the second point When the degree (L ^* , a ^* , b ^* ) is (L3, a3, b3), L3 is 62.5 or more and 80.5 or less, a3 is −1.8 or more and 5.5 or less, b3 is 4.8 to 21.8, L1 <L3 <L2, a1>a3> a2, and b1>b3> b2.

According to the preferred form of the second viewpoint, the color by the L ^* a ^* b ^* color system of the fourth point between the third point and the second point on the straight line connecting the first point to the second point When the degree (L ^* , a ^* , b ^* ) is (L4, a4, b4), L4 is 69.1 or more and 82.3 or less, a4 is −2.1 or more and 1.8 or less, b4 is 3.5 or more and 16.2 or less, a1>a3>a4> a2, and b1>b3>b4> b2.

  According to a preferred form of the second viewpoint, the third point is at a distance of 45% of the total length from one end. The fourth point is at a distance of 55% of the total length from one end.

According to the preferred form of the second viewpoint, at the first point, the third point, the fourth point, and the second point, the difference between the L ^* values at two adjacent points is ΔL ^*, and a ^{* at} the two adjacent points ^. the difference between the value and .DELTA.a ^*, if the difference in ^{b *} values in 2 adjacent points and [Delta] b ^*, which was calculated from the Delta] E ^* ab formula 1 below, the first point and the Delta] E ^* ab between a third point 3 7 to 14.3, ΔE ^* ab between the third point and the fourth point is 1.8 to 17.9 and ΔE ^* ab between the fourth point and the second point is 1.0. It is 9.0 or less.

Formula 1

According to the preferred form of the second viewpoint, on the straight line connecting the first point to the second point, the color by the L ^* a ^* b ^* color system of the third point between the first point and the second point When the degree (L ^* , a ^* , b ^* ) is (L3, a3, b3), L3 is 69.1 or more and 82.3 or less, a3 is -2.1 or more and 1.8 or less, b3 is 3.5 or more and 16.2 or less, L1 <L3 <L2, a1>a3> a2, and b1>b3> b2.

According to the preferred form of the second viewpoint, the color changes in the first direction from one end to the other end, and the color according to the L ^* a ^* b ^* color system on the straight line from the one end to the other end. The tendency to increase or decrease the degree does not change.

According to the preferred form of the second viewpoint, the L ^* value tends to increase from the first point toward the second point on the straight line connecting the one end and the other end, and the a ^* value and the b ^* value decrease. There is a tendency.

  According to the preferable form of the second viewpoint, the distance from one end to the other end is 5 mm to 18 mm.

  According to the preferable form of the second viewpoint, the color does not change along the second direction orthogonal to the first direction.

According to the preferred form of the second viewpoint, at two points on the straight line extending in the second direction, the difference in L ^* value between the two points is ΔL ^*, and the difference in the a ^* value between the two points is Δa. ^{When *} and a difference in b ^* value between two points is Δb ^* and ΔE ^* ab is calculated from Equation 1 above, ΔE ^* ab is less than 1.

  According to a preferred form of the second aspect, the bending strength measured according to JIS R1601 is 1000 MPa or more.

According to a preferred form of the second aspect, the fracture toughness measured according to JIS R1607 is 3.5 MPa · m ^1/2 or more.

  According to a preferred embodiment of the second aspect, in the X-ray diffraction pattern of the zirconia sintered body after being subjected to a hydrothermal test at 180 ° C. and 1 MPa for 5 hours, [111] derived from a tetragonal crystal having 2θ of around 30 °. The ratio of the height of the peak existing near the position where the [11-1] peak derived from the monoclinic crystal having 2θ of about 28 ° to the height of the peak existing near the position where the peak occurs is 1 or less.

  According to a preferred form of the fifth aspect, the cutting is performed using a CAD / CAM system.

  In the present invention, for example, when the zirconia sintered body has a crown shape, the “one end” and the “other end” preferably refer to one point on the cut end side and one point on the root side. The one point may be one point on the end face or one point on the cross section. The point in the section from one end or the other end to 25% of the total length means, for example, a point separated from the one end or the other end by a distance corresponding to 10% of the height of the crown.

  When the zirconia sintered body has a hexahedral shape such as a disk shape or a rectangular parallelepiped, the “one end” and the “other end” preferably refer to one point on the upper surface and the lower surface (bottom surface). The one point may be one point on the end face or one point on the cross section. The point in the section from one end or the other end to 25% of the total length means a point separated from the one end or the other end by a distance corresponding to 10% of the thickness of the hexahedron or the disc.

  In the present invention, the “first direction from one end to the other end” means the direction in which the color changes. For example, the first direction is preferably a direction in which powders in the manufacturing method described later are stacked. For example, when the zirconia sintered body has a crown shape, the first direction is preferably a direction connecting the cut end side and the root side.

  The zirconia calcined body and composition of the present invention will be described. The zirconia calcined body and the composition of the present invention are a composition and a calcined body for producing the zirconia sintered body of the present invention, and a precursor (intermediate product) of the zirconia sintered body of the present invention described later and It will be. The calcined body is obtained by firing (that is, calcining) the composition at a temperature that does not lead to sintering. In addition, the calcined body includes a molded product. For example, a dental prosthesis (for example, a crown shape) obtained by processing a calcined zirconia disk with a CAD / CAM (Computer-Aided Design / Computer-Aided Manufacturing) system is also included in the calcined body.

  The composition and calcined body of the present invention are prepared by laminating zirconia powders having different compositions.

  The composition and calcined body contain (mainly monoclinic) zirconia crystal particles, a stabilizer, and titanium oxide. The composition may contain aluminum oxide. The aluminum oxide is preferably α-alumina.

  The average particle diameter of the zirconia powder (granular state) in the composition is preferably 20 μm to 40 μm.

Examples of the stabilizer in the composition and calcined body include oxides such as calcium oxide (CaO), magnesium oxide (MgO), yttria, and cerium oxide (CeO ₂ ). The stabilizer is preferably added in such an amount that the zirconia particles in the sintered body can be partially stabilized. For example, when using yttria as a stabilizer, the content of yttria is preferably 2.5 mol% to 4.5 mol% with respect to the total number of moles of zirconia and yttria, and 3 mol% to 4.5 mol%. It is preferable and it is more preferable in it being 3.5 mol%-4.5 mol%.

  The content of aluminum oxide in the composition and the calcined body is preferably 0% by mass (not contained) to 0.3% by mass with respect to the total mass of the zirconia crystal particles and the stabilizer. This is to increase the strength of the zirconia sintered body. If it is more than 0.3% by mass, the transparency of the zirconia sintered body is lowered.

  The content of titanium oxide in the composition and the calcined body is preferably 0% by mass (no content) to 0.6% by mass with respect to the total mass of the zirconia crystal particles and the stabilizer. This is for growing grains of zirconia crystals. If it is more than 0.6% by mass, the strength of the zirconia sintered body will decrease.

In the composition and calcined body of the present invention, the content of silicon oxide is preferably 0.1% by mass or less with respect to the total mass of the zirconia crystal particles and the stabilizer, It is preferable that silicon oxide (SiO ₂ ; silica) is not substantially contained. This is because when the silicon oxide is contained, the transparency of the zirconia sintered body is lowered. Here, “substantially does not contain” means within a range that does not particularly affect the properties and characteristics of the present invention, and preferably means that it does not exceed the impurity level, and is not necessarily below the detection limit. Not that there is.

The composition and calcined body of the present invention may contain a pigment for coloring. For example, when a zirconia sintered body produced from the composition of the present invention and a calcined body is applied to a dental material, examples of the pigment include chromium oxide (Cr ₂ O ₃ ) and erbium oxide (Er ₂ O). ₃ ), iron oxide (Fe ₂ O ₃ ), praseodymium oxide (Pr ₆ O ₁₁ ), and the like can be used. These pigments may be used in combination. The pigment content can be partially varied.

  For example, in the molded composition and calcined body, the whole is divided into four layers, and the region of 25% to 45% of the total thickness from the lower end is the first layer, the total thickness on the first layer 5% to 25% of the area on the second layer, on the second layer, 5% to 25% of the total thickness on the third layer, and from the top to the top of the third layer, When the region of 25% to 45% of the entire thickness is the fourth layer, it is preferable that the pigment content decreases from the first layer to the fourth layer.

  For example, when using the sintered compact manufactured from the composition and the calcined body as a dental material, erbium oxide and iron oxide can be added as a pigment. In this case, in the first layer, the content of erbium oxide is 0.33 mass% to 0.52 mass% with respect to the total mass of zirconia and stabilizer, and the content of iron oxide is 0.05. It is preferable that it is mass%-0.12 mass%. In the second layer, the erbium oxide content is 0.26% to 0.45% by mass and the iron oxide content is 0.04% by mass to the total mass of zirconia and stabilizer. The content is preferably 0.11% by mass. In the third layer, the erbium oxide content is 0.05% to 0.24% by mass and the iron oxide content is 0.012% by mass to the total mass of zirconia and stabilizer. It is preferable in it being 0.08 mass%. In the fourth layer, the erbium oxide content is 0% by mass to 0.17% by mass and the iron oxide content is 0% by mass to 0.07% by mass with respect to the total mass of zirconia and the stabilizer. % Is preferable. It is preferable that the contents of erbium oxide and iron oxide decrease in order from the first layer to the fourth layer.

  For example, when using the sintered compact manufactured from the composition and the calcined body as a dental material, erbium oxide, iron oxide and chromium oxide can be added as a pigment. For example, when using the sintered compact manufactured from the composition and the calcined body as a dental material, the content of erbium oxide in the first layer is 0. 0 relative to the total mass of zirconia and stabilizer. The content of iron oxide is 0.08 mass% to 0.15 mass%, and the content of chromium oxide is 0.0008 mass% to 0.0012 mass%. Preferably there is. In the second layer, the content of erbium oxide is 0.06% by mass to 0.42% by mass and the content of iron oxide is 0.06% by mass to the total mass of zirconia and stabilizer. It is 0.18 mass%, and it is preferable in the content rate of chromium oxide being 0.0006 mass%-0.001 mass%. In the third layer, the erbium oxide content is 0.06% by mass to 0.17% by mass and the iron oxide content is 0.018% by mass to the total mass of zirconia and stabilizer. It is 0.042 mass%, and it is preferable in the content rate of chromium oxide being 0.0001 mass%-0.0003 mass%. In the fourth layer, the erbium oxide content is 0% by mass to 0.12% by mass and the iron oxide content is 0% by mass to 0.001% by mass with respect to the total mass of zirconia and the stabilizer. %, And the chromium oxide content is preferably 0% by mass to 0.0001% by mass. The contents of erbium oxide, iron oxide, and chromium oxide are preferably decreased in order from the first layer to the fourth layer.

  For example, when using the sintered compact manufactured from the composition and the calcined body as a dental material, erbium oxide, iron oxide, and praseodymium oxide can be added as pigments. For example, when using the sintered compact manufactured from the composition and the calcined body as a dental material, the content of erbium oxide in the first layer is 0. 0 relative to the total mass of zirconia and stabilizer. It is 08 mass% to 2.2 mass%, the content of iron oxide is 0.003 mass% to 0.12 mass%, and the content of praseodymium oxide is 0.003 mass% to 0.12 mass%. Preferably there is. In the second layer, the content of erbium oxide is 0.06% by mass to 1.9% by mass and the content of iron oxide is 0.002% by mass to the total mass of zirconia and stabilizer. It is 0.11 mass%, and it is preferable in the content rate of praseodymium oxide being 0.002 mass%-0.11 mass%. In the third layer, the erbium oxide content is 0.018% by mass to 1% by mass and the iron oxide content is 0.008% by mass to 0.00% with respect to the total mass of zirconia and the stabilizer. It is 06 mass%, and it is preferable in the content rate of praseodymium oxide being 0.0008 mass%-0.06 mass%. In the fourth layer, the content of erbium oxide is 0% by mass to 0.7% by mass and the content of iron oxide is 0% by mass to 0.05% by mass with respect to the total mass of zirconia and the stabilizer. %, And the praseodymium oxide content is preferably 0% by mass to 0.05% by mass. The contents of erbium oxide, iron oxide, and praseodymium oxide are preferably decreased in order from the first layer to the fourth layer.

  The pigment content can be theoretically calculated from the amount of the zirconia and the stabilizer added relative to the total mass and the production method.

  About the calcined body of this invention, the bending strength measured based on JISR1601 is preferable in it being 38 MPa or more, it is more preferable in it being 40 MPa or more, and it is further more preferable in it being 42 MPa or more.

  In the calcined body of the present invention, in the three-point bending test, as shown in the manufacturing method described later, the load point is located at the boundary between layers when zirconia powders having different compositions are laminated. However, the bending strength can be obtained. For example, when the bending strength is measured by the same test as the bending test of a sintered body described later, higher strength can be obtained as compared with a calcined body produced by simply laminating powders. Moreover, even if the bending strength is measured by a test in which a load is applied to the boundary, the same strength as that of a calcined body that is not laminated (without a boundary) can be obtained. In the calcined body of the present invention, the bending strength measured by applying a load to the boundary between layers is the bending strength of the region other than the boundary (for example, the same conditions (for example, the same calcining temperature and 90% or more of the bending strength) of the calcined body produced in (time), and more preferably 95% or more.

  Even if the composition and calcined body of the present invention are subjected to heat treatment for calcining or sintering, there is no separation at the boundary between layers in which zirconia powders having different compositions are laminated. Can also be suppressed. The schematic diagram of the test piece for measuring the deformation amount at the time of sintering in FIG.1 and FIG.2 is shown. FIG. 1 is a schematic view of a two-layer laminate. FIG. 2 is a schematic diagram of a four-layer laminate. In FIG. 3, the schematic diagram for demonstrating the measuring method of deformation is shown. For example, a plurality of zirconia powders having different compositions are laminated to form a composition, and the composition is fired at 800 ° C. to 1200 ° C. for 2 hours to prepare a calcined body. And as shown in FIG.1 and FIG.2, a calcined body is shape | molded by the CAD / CAM system in the rectangular parallelepiped shape of a dimension of width 50mm * height 10mm * depth 5mm. This becomes a test piece. For example, a two-layer test piece 20 shown in FIG. 1 has a first layer 21a and a second layer 21b. The thickness of the first layer 21a and the thickness of the second layer 21b are 50% of the total thickness, respectively. The test piece 22 of a four-layer laminate shown in FIG. 2 has a first layer 23a, a second layer 23b, a third layer 23c, and a fourth layer 23d. The thicknesses of the first layer 23a and the fourth layer 23d are 35% of the total thickness. The thickness of the second layer 23b and the third layer 23c is 15% of the total thickness. When the 50 mm × 5 mm surface of the test pieces 20 and 22 is a bottom surface (upper surface and lower surface), each layer extends in the same direction as the bottom surfaces 20 a and 22 a, and preferably extends in parallel. That is, the boundary between the layers is parallel to the bottom surfaces 20a and 22a. When this test piece is fired at 1500 ° C. for 2 hours and sintered, the bottom surfaces 20a and 22a are deformed so as to be curved. The test pieces 20 and 22 are placed on a flat place (grounding surface 30) with the concave surface of the bottom surfaces 20a and 22a facing down. And the width | variety after the test pieces 20 and 22 deform | transformed, ie, the distance L between the grounding parts in the width direction, is measured. Further, the distance d of the largest portion among the distances between the bottom surfaces 20a, 22a deformed into the concave surface and the grounding surface 30 is measured. Then, the deformation amount is calculated as (d / L × 100). The amount of deformation is preferably 0.15 or less, more preferably 0.1 or less, more preferably 0.05 or less, and further preferably 0.03 or less.

  Compositions and calcined bodies prepared by laminating zirconia powders having different compositions are easily deformed when sintered. However, according to the composition and calcined body of the present invention, Compared to the calcined body, the amount of deformation can be reduced. Thereby, the dimensional accuracy of the final product can be increased. For example, the composition and calcined body of the present invention can be suitably applied to a dental prosthesis having a large individual difference. In FIGS. 1 and 2, the upper and lower mixed layers presumed to be formed at the boundaries of the layers are not shown for the sake of simplicity.

  The composition of the present invention includes a powder, a fluid obtained by adding the powder to a solvent, and a molded body obtained by molding the powder into a predetermined shape. That is, the composition may be in the form of a powder, or a paste or a wet composition (that is, it may be in a solvent or may contain a solvent). The composition may contain additives such as a binder and a pigment. In addition, in the calculation of the content rate, the mass of additives such as a solvent and a binder is not considered.

  When the composition of the present invention is a molded body, it may be molded by any molding method, and may be molded by, for example, press molding, injection molding, stereolithography, or multistage. It may be molded. For example, the composition of the present invention may be subjected to press molding and further subjected to CIP (Cold Isostatic Pressing) treatment.

  The calcined body of the present invention can be obtained by firing the composition of the present invention at 800 ° C. to 1200 ° C. under normal pressure.

  The length (thickness) in the stacking direction of the composition and the calcined body is preferably determined so as to realize the target length of the sintered body in consideration of sintering shrinkage. For example, when using the sintered compact manufactured from the composition and the calcined body as a dental material, for example, the length of the target sintered body in the stacking direction is 5 mm to 18 mm, and the composition and the calcined body The length (thickness) in the stacking direction can be set to 10 mm to 26 mm.

  Next, the zirconia sintered body of the present invention will be described. The zirconia sintered body of the present invention is a sintered body in which partially stabilized zirconia crystal particles are mainly sintered, and has partially stabilized zirconia as a matrix phase. In the zirconia sintered body of the present invention, the main crystal phase of zirconia is tetragonal or tetragonal and cubic. It is preferable that the zirconia sintered body does not substantially contain a monoclinic system (in a hydrothermal test untreated stage described later).

  The zirconia sintered body of the present invention includes not only a sintered body obtained by sintering molded zirconia particles under normal pressure or non-pressurization, but also HIP (Hot Isostatic Pressing) treatment, etc. A sintered body densified by high-temperature pressure treatment is also included.

The zirconia sintered body of the present invention contains zirconia and its stabilizer. The stabilizer suppresses the phase transition of tetragonal zirconia to the monoclinic system. By suppressing the phase transition, strength, durability and dimensional accuracy can be increased. Examples of the stabilizer include oxides such as calcium oxide (CaO), magnesium oxide (MgO), yttrium oxide (Y ₂ O ₃ ) (hereinafter referred to as “yttria”), and cerium oxide (CeO ₂ ). It is done. The stabilizer is preferably added in such an amount that the tetragonal zirconia particles can be partially stabilized. For example, when using yttria as a stabilizer, the yttria content is preferably 2.5 mol% to 5 mol% with respect to the total number of moles of zirconia and yttria, and is 3 mol% to 4.5 mol%. More preferably, it is 3.5 mol%-4.5 mol%. When the content of the stabilizer is increased too much, the bending strength and fracture toughness are lowered even if the phase transition can be suppressed. On the other hand, if the content of the stabilizer is too low, the progress of the phase transition is not sufficiently suppressed even if the decrease in bending strength and fracture toughness can be suppressed. Note that tetragonal zirconia partially stabilized by adding a stabilizer is called partially stabilized zirconia (PSZ).

The zirconia sintered body of the present invention preferably contains aluminum oxide (Al ₂ O ₃ ; alumina). The aluminum oxide is preferably α-alumina. If aluminum oxide is contained, the strength can be increased. The content of aluminum oxide in the zirconia sintered body is preferably 0% by mass (not contained) to 0.3% by mass with respect to the total mass of zirconia and the stabilizer. When the aluminum oxide is contained in an amount of more than 0.3% by mass, the transparency is lowered.

The zirconia sintered body of the present invention preferably contains titanium oxide (TiO ₂ ; titania). When titanium oxide is contained, grain growth can be promoted. The content of titanium oxide in the zirconia sintered body is preferably 0% by mass (not contained) to 0.6% by mass with respect to the total mass of zirconia and the stabilizer. If titanium oxide is contained in an amount of more than 0.6% by mass, the strength is lowered.

In the zirconia sintered body of the present invention, the content of silicon oxide (SiO ₂ ; silica) is preferably 0.1% by mass or less based on the total mass of zirconia and the stabilizer, It is preferable that silicon oxide is not substantially contained. This is because when the silicon oxide is contained, the transparency of the zirconia sintered body is lowered. Here, “substantially does not contain” means within a range that does not particularly affect the properties and characteristics of the present invention, and preferably means that it does not exceed the impurity level, and is not necessarily below the detection limit. Not that there is.

The zirconia sintered body of the present invention may contain a coloring pigment. When the zirconia sintered body is applied to a dental material, examples of the pigment include chromium oxide (Cr ₂ O ₃ ), erbium oxide (Er ₂ O ₃ ), iron oxide (Fe ₂ O ₃ ), and praseodymium oxide (Pr). ₆ O ₁₁ ) or the like can be used. These pigments may be used in combination. The pigment content can be partially varied.

  For example, when the zirconia sintered body used as the dental material contains chromium oxide, the partial content of chromium oxide in the region containing chromium oxide is 0. 0% with respect to the total mass of zirconia and stabilizer. It is preferable that it is 001 mass% or less. When the zirconia sintered body used as a dental material contains erbium oxide, the partial content of erbium oxide in the region containing erbium oxide is 2% by mass or less based on the total mass of zirconia and the stabilizer. Is preferable. For example, when the zirconia sintered body used as the dental material contains iron oxide, the partial content of iron oxide in the region containing iron oxide is 0. 0 relative to the total mass of zirconia and the stabilizer. It is preferable that it is 1 mass% or less. For example, when the zirconia sintered body used as a dental material contains praseodymium oxide, the partial content of praseodymium oxide in the region containing praseodymium oxide is 0. 0 relative to the total mass of zirconia and stabilizer. It is preferable that it is 1 mass% or less.

  After the sintering of the zirconia sintered body, in the X-ray diffraction pattern measured by CuKα ray of the hydrothermal treatment test (described later), an untreated zirconia sintered body, which is an accelerated deterioration test, 2θ is derived from a tetragonal crystal having a vicinity of 30 °. It exists in the vicinity of the position where the [11-1] peak derived from the monoclinic crystal having 2θ of about 28 ° relative to the height of the peak existing in the vicinity of the position where the [111] peak occurs (hereinafter referred to as “first peak”) The height ratio of peaks (hereinafter referred to as “second peak”) (that is, “second peak height / first peak height”; hereinafter referred to as “monoclinic peak ratio”) is 0.1 Or less, more preferably 0.05 or less.

  In the zirconia sintered body of the present invention, the progress of the phase transition from tetragonal to monoclinic is suppressed even when subjected to a hydrothermal treatment test. For example, when hydrothermal treatment at 180 ° C. and 1 MPa for 5 hours is performed on the zirconia sintered body of the present invention, the monoclinic crystal in the X-ray diffraction pattern measured with CuKα rays on the surface of the zirconia sintered body after hydrothermal treatment The peak ratio is preferably 1 or less, more preferably 0.8 or less, still more preferably 0.7 or less, and even more preferably 0.6 or less.

  In this document, the “hydrothermal treatment test” refers to a test based on ISO13356. However, the conditions defined in ISO 13356 are “134 ° C., 0.2 MPa, 5 hours”. However, in the present invention, the test conditions are set to “180 ° C., 1 MPa” in order to make the test conditions more severe. The test time is appropriately set according to the purpose. The hydrothermal treatment test is also called a “low temperature deterioration acceleration test” or a “hydrothermal deterioration test”.

  About the zirconia sintered compact of this invention, the bending strength measured based on JISR1601 is preferable in it being 1000 MPa or more, it is more preferable in it being 1100 MPa or more, and it is further more preferable in it being 1200 MPa or more. In addition, these are numerical values in a state where the hydrothermal treatment test is not performed.

  In the zirconia sintered body of the present invention, in the three-point bending test, the bending strength can be obtained even when a load point is located at a boundary portion between layers in a manufacturing method described later. FIG. 4 shows a schematic diagram of a three-point bending test. For example, in the test piece, the boundary when the zirconia powders having different compositions are laminated is located at the center (the middle in the longitudinal direction) of the test piece. The boundary extends along the load application direction (along the smallest area direction) and crosses the test piece. The load point of the three-point bending test is adjusted to the position of the boundary. Thus, even if the bending strength is measured by a test in which a load is applied to the boundary, it is possible to obtain the same strength as a sintered body that is not laminated (without a boundary). For example, in the sintered body of the present invention, the bending strength measured by applying a load to the boundary between layers is the bending strength in a region other than the boundary (for example, the same conditions (for example, the same calcining temperature / 90% or more of the bending strength of the calcined body produced in the calcining time), and more preferably 95% or more.

For zirconia sintered body of the present invention, fracture toughness was measured according to JISR1607 is preferable to be 3.5 MPa ^{· m 1/2} or more, more preferably 3.8 MPa ^{· m 1/2} or more, 4 MPa · More preferably, it is m ^1/2 or more, and more preferably 4.2 MPa · m ^1/2 or more. In addition, these are numerical values in a state where the hydrothermal treatment test is not performed.

  In the zirconia sintered body of the present invention, in the fracture toughness measurement test, the fracture toughness can be obtained even when the load point is located at the boundary between layers in the manufacturing method described later. For example, in the test piece, the boundary when the zirconia powders having different compositions are laminated is located at the center (the middle in the longitudinal direction) of the test piece. The boundary extends along the load application direction (along the smallest area direction) and crosses the test piece. The position of the diamond indenter in the measurement test is set on the boundary. In this way, even when the fracture toughness is measured by a test in which a load is applied to the boundary, the same fracture toughness as a non-laminated (no boundary) sintered body can be obtained.

The zirconia sintered body of the present invention preferably satisfies the above numerical values for the monoclinic peak ratio after hydrothermal treatment, bending strength, and fracture toughness. For example, the zirconia sintered body of the present invention has a monoclinic peak ratio after hydrothermal treatment of 1 or less, a fracture toughness of 3.5 MPa · m ^1/2 or more, and a bending strength of 1000 MPa or more. preferable. More preferably, in the zirconia sintered body of the present invention, the monoclinic peak ratio after hydrothermal treatment is 0.6 or less, the fracture toughness is 4 MPa · m ^1/2 or more, and the bending strength is 1000 MPa or more. is there.

Even when the zirconia sintered body of the present invention is colored, particularly when the color gradually changes in one direction (becomes a gradation), the zirconia sintered body of the present invention has a color. It is preferable that there is a direction in which does not substantially change. In FIG. 5, the schematic diagram of a zirconia sintered compact is shown. For example, in the zirconia sintered body 10 shown in FIG. 5, it is preferable that the color does not substantially change in the first direction X. For example, between any two points on a straight line extending in the first direction X, the difference between the L ^* value, a ^* value, and b ^* value, which are chromaticities in the L ^* a ^* b ^* color system (JISZ8729) the [Delta] L ^*, respectively, and .DELTA.a ^* and [Delta] b ^*, when calculating the Delta] E ^* ab of the following formula, preferably a Delta] E ^* ab is less than 1, more preferably less than 0.5.

Formula 2

Moreover, when the zirconia sintered body of the present invention is colored, it is preferable that the color changes from one end connecting both ends to the other end (has gradation). On the straight line extending in the second direction Y from one end P to the other end Q of the zirconia sintered body 10 shown in FIG. 5, the increasing or decreasing tendency of the L ^* value, a ^* value, and b ^* value is in the reverse direction. It is preferable if it does not change. That is, if the L ^* value on a straight line toward the other Q from one end P is increasing, the L ^* value is not substantially reduced interval exists preferred. For example, if the L ^* value on a straight line toward the other Q from one end P is increasing, preferably the L ^* value is no section to reduce one or more, if there is no section that decreases 0.5 or more preferable. When the a ^* value tends to decrease on the straight line from the one end P to the other end Q, it is preferable that there is no section in which the a ^* value substantially increases. For example, if the a ^* value on a straight line toward the other Q from one P is decreasing, preferably when there is no section where the a ^* value increases by one or more, if there is no section to increase 0.5 or more preferable. Also, if the b ^* value is decreasing on a straight line toward the other Q from one end P, when the b ^* value does not substantially increase the interval to present preferred. For example, if the b ^* value is decreasing on a straight line toward the other Q from one end P, preferably the b ^* value does not exist interval increase of 1 or more, the absence of section to be increased by 0.5 or more and more preferable.

The direction of color change in the zirconia sintered body 10 is preferably such that when the L ^* value tends to increase from one end P to the other end Q, the a ^* value and b ^* value tend to decrease. For example, when the zirconia sintered body 10 is used as a dental prosthetic material, it is preferable to change from light yellow, light orange, or light brown toward the white direction from one end P to the other end Q.

  In FIG. 5, points on a straight line connecting one end P to the other end Q are defined as a first point A, a second point B, a third point C, and a fourth point D in this order from the one end P side. When the zirconia sintered body 10 is used as a dental prosthetic material, the first point A is from one end P to 25% to 45% of the length between the one end P and the other end Q (hereinafter referred to as “full length”). It is preferable to be in the section. The second point B is preferably in a section from one end P to 30% of the total length from a position 30% away from the total length. The fourth point D is preferably in the section from the other end Q to 25% to 45% of the entire length. The third point C is preferably in a section from the other end Q to 30% of the total length from a position 30% away from the other end Q.

Chromaticity (L ^* , a ^* , b ^* ) of the zirconia sintered body 10 according to the L ^* a ^* b ^* color system (JISZ8729) at the first point A, the second point B, the third point C, and the fourth point D ) Are (L1, a1, b1), (L2, a2, b2), (L3, a3, b3) and (L4, a4, b4). At this time, it is preferable that the following magnitude relationship is established. In addition, the chromaticity of each point can be calculated | required by producing the zirconia sintered compact of the composition corresponding to each point, and measuring the chromaticity of the said zirconia sintered compact.

L1 <L2 <L3 <L4
a1>a2>a3> a4
b1>b2>b3> b4

  When the zirconia sintered body of the present invention is applied to a dental material, for example, L1 is preferably 58.0 or more and 76.0 or less. L2 is preferably 62.5 or more and 80.5 or less. L3 is preferably 69.1 or more and 82.3 or less. L4 is preferably 71.8 or more and 84.2 or less.

  When the zirconia sintered body of the present invention is applied to a dental material, for example, a1 is preferably −1.6 or more and 7.6 or less. a2 is preferably −1.8 or more and 5.5 or less. a3 is preferably −2.1 or more and 1.6 or less. a4 is preferably -2.1 or more and 1.8 or less.

  When the zirconia sintered body of the present invention is applied to a dental material, for example, b1 is preferably from 5.5 to 26.7. b2 is preferably 4.8 or more and 21.8 or less. b3 is preferably 3.5 or more and 16.2 or less. b4 is preferably 1.9 or more and 16.0 or less.

  When the zirconia sintered body of the present invention is applied to a dental material, preferably, L1 is 60.9 or more and 72.5 or less, a1 is 0.2 or more and 5.9 or less, and b1 is 11.5. 24.9 or less, L4 is 72.2 or more and 79.2 or less, a4 is −1.2 or more and 1.7 or less, and b4 is 6.0 or more and 15.8 or less. More preferably, L1 is 63.8 or more and 68.9 or less, a1 is 2.0 or more and 4.1 or less, b1 is 17.5 or more and 23.4 or less, and L4 is 72.5 or more and 74. 0.1 or less, a4 is −0.2 or more and 1.6 or less, and b4 is 10.1 or more and 15.6 or less. As a result, the color tone of the average tooth can be adapted.

The color difference ΔE ^* ab between two adjacent points can be expressed by the following equation. ΔL ^* is a difference between L ^* values in two adjacent layers (for example, L1−L2). Δa ^* is a difference between a ^* values in two adjacent layers (for example, a1−a2). Δb ^* is a difference between b ^* values in two adjacent layers (for example, b1−b2). The color difference between the first point A and the second point B is ΔE ^* ab1, the color difference between the second point B and the third point C is ΔE ^* ab2, and the color difference between the third point C and the fourth point D is ΔE ^* ab3. When the chromaticity of the first point A, the second point B, the third point C, and the fourth point D has the above relationship, for example, ΔE ^* ab1 is preferably 3.7 or more and 14.3 or less. ΔE ^* ab2 is preferably 1.8 or more and 17.9 or less. ΔE ^* ab3 is preferably 1.0 or more and 9.0 or less. Thereby, the color change similar to a natural tooth can be reproduced.

Formula 3

When the color difference between the first point A and the fourth point D is ΔE ^* ab4, when the chromaticity of the first point A, the second point B, the third point C, and the fourth point D has the above relationship, ΔE ^* ab4 is preferably 36 or less. Color difference Delta] E ^* ab1 the first point A and the second point B, and the sum of the color difference Delta] E ^* ab2 and the three points C and a fourth point color difference Delta] E ^* ab3 of the second point B and the third point C, the first point The value obtained by subtracting the color difference ΔE ^* ab4 between A and the fourth point D is preferably 1 or less. Thereby, a natural color change can be shown.

In the zirconia sintered body of the present invention, the second direction Y shown in FIG. 5 is linear, so as to cross the layer when the powders having different compositions are laminated in the manufacturing method described later (so as to cross the boundary). When the continuous change in the b ^* value of the L ^* a ^* b ^* color system (JISZ8729) along the line is measured, the b ^* value does not become constant even when crossing the layer, and it gradually increases (or decreases) (Tendency) is preferable. Further, even when the boundary portion is crossed, it is preferable that no sudden increase or decrease in the b ^* value is observed. The change in the b ^* value can be measured using, for example, a two-dimensional color meter RC-300 of Paparabo Co., Ltd. In this measurement, the interval between adjacent measurement points can be set to 13 μm, for example.

  When the zirconia sintered body of the present invention is applied to a dental material, if the chromaticity of the fourth point D is in the above range, a zirconia sintered body is produced with the composition alone corresponding to the fourth point, The light transmittance measured by making a mirror-finished 0.5 mm thick sample according to JIS K 7361 is preferably 27% or more. In addition, when the chromaticity of the first point A is in the above range, a zirconia sintered body is prepared with the composition corresponding to the first point alone, and a sample having a thickness of 0.5 mm is prepared by mirror-processing both surfaces. The light transmittance measured according to JISK7361 is preferably 10% or more.

  When the zirconia sintered body of the present invention is applied to a dental material, it is preferable that the length L in the first direction Y of the zirconia sintered body 10 of the present invention satisfies at least the length corresponding to the exposed portion of natural teeth. . For example, the length L of the zirconia sintered body 10 is preferably 5 mm to 18 mm.

  The sintered body of the present invention can be produced by firing the calcined body or composition of the present invention at 1350 ° C. to 1600 ° C. under normal pressure.

  Next, an example of the manufacturing method of the composition of this invention, a calcined body, and a sintered compact is demonstrated. Here, a method of gradually changing the color of the sintered body (gradation) will also be described.

  First, zirconia and a stabilizer are wet mixed in water to form a slurry. Next, the slurry is dried and granulated. Next, the granulated product is calcined to produce a primary powder.

  Next, when adding gradation to the sintered body, the primary powder is divided into two. Next, the pigment is added to at least one of the two primary powders so that a difference occurs in the pigment addition rate. For example, no pigment may be added to one, and a pigment may be added to the other. Hereinafter, a powder having a lower addition rate of a specific pigment is referred to as a low addition rate powder, and a secondary powder having a higher addition rate of the specific pigment is referred to as a high addition rate powder. The addition amount of the pigment in the high addition rate powder is preferably matched to the addition amount in the darkest region of the sintered body. And about each, zirconia is grind | pulverized and mixed until it becomes a desired particle size in water, and a zirconia slurry is formed. Next, the slurry is dried and granulated to produce a secondary powder. When an additive such as aluminum oxide, titanium oxide, or a binder is added, it may be added when producing the primary powder, or may be added when producing the secondary powder.

  Next, based on the secondary powder of the low addition rate powder and the high addition rate powder, a plurality of powders having different pigment content ratios are prepared. For example, when producing the above-mentioned composition and calcined body of a total of 4 layers, the 1st powder for the 1st layer is made into 100% of high addition rate powder, without mixing low addition rate powder. The second powder for the second layer is mixed in a ratio of low addition rate powder: high addition rate powder = 5: 95 to 15:85. The third powder for the third layer is mixed at a ratio of low addition rate powder: high addition rate powder = 35: 65 to 45:55. The fourth powder for the fourth layer is mixed at a ratio of low addition rate powder: high addition rate powder = 45: 55 to 55:45. As another mixing ratio, for example, in the case of producing the above-described total four-layer composition and calcined body, the first powder for the first layer is not mixed with the low addition rate powder, but the high addition rate powder 100. %. The second powder for the second layer is mixed at a ratio of low addition rate powder: high addition rate powder = 10: 90 to 30:70. The third powder for the third layer is mixed at a ratio of low addition rate powder: high addition rate powder = 70: 30 to 90:10. The fourth powder for the fourth layer is made into a low addition rate powder 100% without mixing the high addition rate powder.

  When the zirconia sintered body is used for a dental material, it is preferable that the blending difference between the second layer and the third layer is larger than the blending difference between the first layer and the second layer and the blending difference between the third layer and the fourth layer. Thereby, the color change similar to a natural tooth can be reproduced.

  In this way, by adjusting the pigment content of each layer based on two types of powders in which the sintered body exhibits different colors, the colors can be naturally changed by sequentially laminating each powder (gradation). Can produce).

  When laminating for purposes other than coloring, it is divided into the number of layers on which the secondary powder is laminated. A desired additive may be added to each powder.

  Next, a plurality of powders having different pigment contents are sequentially laminated. When gradation is formed on the sintered body, it is preferable that the layers are laminated so that the addition rate of a specific pigment increases or decreases stepwise in the order of lamination. First, after filling the mold with the first layer of powder, the upper surface of the first layer of powder is flattened. As a method of leveling the surface flat, for example, a method of vibrating a mold or scraping the upper surface of the first layer of powder can be employed. However, it is preferable that the press treatment is not performed until all the layers are laminated. Next, the powder of the second layer is filled on the powder of the first layer. Next, a vibration is given to the mold. The vibration is transmitted to the powder in the mold. As a method for applying vibration, for example, a mechanical vibration can be applied to the mold, the mold can be shaken manually, or the mold can be struck with a hammer or the like. Thereby, it is considered that the powder of the first layer and the powder of the second layer are partially mixed at the boundary between the powder of the first layer and the powder of the second layer. That is, in the case of mechanical vibration, the frequency, amplitude, etc. of the vibration are such that the powder particle size, particle size distribution, particle shape, etc. It can be set appropriately depending on the situation. Next, the upper surface of the second layer powder is leveled in the same manner as the first layer powder. This operation is repeated until all layers are laminated.

  For example, when producing the above-mentioned total of four layers of composition and calcined body, the mold is filled with the first powder to a predetermined thickness (for example, 25% to 45% of the total thickness). At this time, the upper surface of the first powder is leveled, but no press treatment is performed. Next, the second powder is filled on the first powder to a predetermined thickness (for example, 5% to 25% of the total thickness). Next, a vibration is given to the mold. This vibration is presumed to form a first boundary layer in which the first powder and the second powder are mixed at the boundary between the upper surface of the first powder and the lower surface of the second powder. Next, the upper surface of the second powder is leveled flat. Prior to filling the third powder, the second powder is not pressed. Next, the third powder is filled on the second powder to a predetermined thickness (for example, 5% to 25% of the total thickness). Next, a vibration is given to the mold. This vibration is presumed to form a second boundary layer in which the second powder and the third powder are mixed at the boundary between the upper surface of the second powder and the lower surface of the third powder. Next, the upper surface of the third powder is leveled flat. Before the fourth powder filling, the third powder is not pressed. Next, the fourth powder is filled on the third powder to a predetermined thickness (for example, 25% to 45% of the total thickness). Next, a vibration is given to the mold. This vibration is presumed to form a third boundary layer in which the third powder and the fourth powder are mixed at the boundary between the upper surface of the third powder and the lower surface of the fourth powder.

  After all the layers are laminated, press molding is performed to produce a molded product as the composition of the present invention. The molded product may be further subjected to CIP treatment.

  By not applying a press treatment before filling the next layer powder and applying vibration every time each layer is filled, a boundary layer in which the upper and lower layer powders are mixed can be formed between adjacent layers. Conceivable. Thereby, in a sintered compact, the adhesiveness between adjacent layers can be improved. The amount of shrinkage or shrinkage rate during heat treatment can be made equal in each layer, preventing peeling between layers during heat treatment, and preventing the sintered body from deforming to the target shape. can do. Furthermore, the color difference between adjacent layers can be reduced. Thereby, in a sintered compact, a color can be naturally changed in the lamination direction (a gradation can be created).

  Further, according to this method, no intermediate layer is required between the main layers. That is, when four main layers are stacked, only four layers need be stacked. Further, no pressing process is required for each layer. Thereby, labor and time can be greatly reduced, and the manufacturing cost can be reduced.

  When the calcined body is not prepared, the zirconia powder is sintered by firing the composition at 1400 ° C. to 1600 ° C., preferably 1450 ° C. to 1550 ° C., to produce the zirconia sintered body of the present invention. . You may shape | mold in a desired shape in the stage of a molding.

  When producing a calcined body, the composition is fired at 800 ° C. to 1200 ° C. to produce a calcined body. Next, the calcined body is fired at 1400 ° C. to 1600 ° C., preferably 1450 ° C. to 1550 ° C., thereby sintering the zirconia powder to produce the zirconia sintered body of the present invention. The molding may be performed by cutting or the like at the stage of the calcined body, or may be performed after sintering. Molding can be performed with a CAD / CAM system.

  The method for producing a dental prosthesis is the same as the method for producing a sintered body, except that the calcined body or the sintered body is formed into a crown shape.

  In the above embodiment, a composition, a calcined body, and a sintered body based on a four-layer laminate are illustrated, but the present invention is not limited to four layers. For example, it may be a composition, a calcined body, and a sintered body prepared from the above-described two-layer laminate of the first layer and the fourth layer. Or a composition, a calcined body, and a sintered body made from the above-described first layer, second layer, and fourth layer, or a three-layer laminate of the first layer, third layer, and fourth layer. May be. Moreover, FIG. 4 is for facilitating the explanation of the positional relationship and direction of each point, and the shape and dimensions are not limited to the form shown in FIG.

[Examples 1 to 4]
[Production of composition, calcined body and sintered body]
A sintered body was prepared based on a composition prepared by laminating zirconia powders having different compositions, and bending strength, chromaticity, and deformation amount were measured.

  First, zirconia powder containing a stabilizer was prepared. Yttria 7.2% by mass (4 mol%) was added as a stabilizer to mainly 92.8% by mass of monoclinic zirconia powder. Alumina sol is added so that 0.1% by mass of alumina is added to the mixed powder of zirconia and yttria (100% by mass), and 150% by mass of water is added to the mixed powder of zirconia and yttria (100% by mass). Then, 0.2% by mass of an antifoaming agent and 1% by mass of a dispersing agent were added, and the mixture was pulverized with a ball mill for 10 hours. The average particle size of the slurry obtained after pulverization was 0.12 μm. Next, it was granulated with a spray dryer, and the resulting granule was calcined at 1000 ° C. for 2 hours to produce a primary powder.

  Next, the primary powder was divided into two and the pigment was added to at least one of them. The lower addition rate of the pigment was defined as the low addition rate powder, and the higher addition rate of the pigment was defined as the high addition rate powder. Table 1 shows the addition rates of Examples 1 to 3. Table 4 shows the addition rate of Example 4. The numerical values shown in Tables 1 and 2 are addition rates with respect to the mixed powder (100% by mass) of zirconia and yttria. In addition, 0.2% by mass of titania, 200% by mass of water, 0.2% by mass of antifoaming agent, and 1% by mass of dispersant are added to each powder with respect to the mixed powder of zirconia and yttria (100% by mass). The mixture was then pulverized with a ball mill for 15 hours. The average particle size of the slurry obtained after pulverization was 0.13 μm. Next, 6% by mass of a binder and 0.5% by mass of a release agent were added and mixed for 15 minutes by a ball mill. Next, the resulting slurry was granulated with a spray dryer to produce a secondary powder of a low addition rate powder and a high addition rate powder.

  Next, the low addition rate powder and the high addition rate powder were mixed in the ratios shown in Tables 3 to 6 to prepare first to fourth powders.

Next, a molded body was produced. In Examples 1, 3, and 4, 35 g of the first powder was filled in a mold having an inner size of 82 mm × 25 mm, and the upper surface was ground to make the upper surface of the first powder flat. Next, 15 g of the second powder was filled on the first powder, and the mold was vibrated by a vibration device. Thereafter, the upper surface of the second powder was ground to flatten the upper surface of the second powder. Next, 15g of 3rd powder was filled on the 2nd powder, and the metal mold | die was vibrated with the vibration apparatus. Thereafter, the upper surface of the third powder was ground to make the upper surface of the third powder flat. Next, 35 g of the fourth powder was filled on the third powder, and the mold was vibrated by the vibration device. Thereafter, the upper surface of the fourth powder was ground to make the upper surface of the fourth powder flat. Example 2 is the same as Examples 1, 3 and 4 except that 50 g of the first powder is filled and 50 g of the second powder is filled. Next, the upper mold was set, and primary press molding was performed for 90 seconds at a surface pressure of 200 kg / cm ² using a uniaxial press molding machine. Next, the primary press-molded body was CIP-molded at 1500 kg / cm ² for 5 minutes to produce a molded body.

  Next, the compact was fired at 1000 ° C. for 2 hours to prepare a calcined body. Next, it was molded into a crown shape using a CAD / CAM system (Katana System, Kurarenoritake Dental Co., Ltd.). Next, the calcined body was fired at 1500 ° C. for 2 hours to produce a sintered body. The length of the sintered body in the stacking direction of the first to fourth powders was 8 mm.

  In any of the sintered bodies of Examples 1 to 4, a gradation changing from light yellow to yellowish white is formed from the region corresponding to the first layer of the composition to the region corresponding to the fourth layer. It had the same appearance as the teeth.

[Measurement of bending strength]
About the calcined body and sintered body produced in Example 4, bending strength was measured based on JISR1601. As a comparative example, the bending strength was also measured for a calcined body and a sintered body that were not vibrated when filling each powder. Comparative Example 1 is a calcined body and a sintered body produced from a composition that is not subjected to press treatment each time each layer is filled. Comparative Example 2 is a calcined body and a sintered body produced from a composition subjected to press treatment each time each layer is filled. The bending strength was measured according to JIS R1601. However, the test piece is cut out in the longitudinal direction along the stacking direction. As shown in FIG. 4, in the test piece, the boundary between the second powder and the third powder was set to the center of the test piece. The boundary extends along the load application direction (along the smallest area direction) and crosses the test piece. The bending strength was measured by aligning the load point of the three-point bending test with the position of the boundary. Table 7 shows the measurement results.

  Regarding the calcined body, the bending strength of Example 4 was 40 MPa or more, while the bending strength of the comparative example was 36 MPa or less. From this, it can be seen that by applying vibration during powder lamination, the bonding strength between the layers can be increased at the stage of the calcined body. The sintered body was 1200 MPa or more in Example 4, but Comparative Examples 1 and 2 were less than 1100 MPa and lower than Example 4 by 100 MPa or more. It can be seen that the bonding strength between the layers can be similarly increased for the sintered body.

  Further, as shown in Example 9 described later, the bending strength of Example 4 is the same as the bending strength of the sintered body produced without lamination in both the sintered body and the calcined body. It can be seen that no decrease in bonding strength has been caused. From this, it can be seen that the boundary between the stacked layers has the same strength as the region other than the boundary in both the sintered body and the calcined body by applying vibration during the powder stacking.

  This is presumably because the upper and lower layer powders are partially mixed at the boundary by applying vibration when the powders of each layer are laminated, thereby increasing the bonding strength between the layers. In addition, secondarily, the first to fourth powders were prepared by mixing two kinds of powders, so that the difference in properties between the powders was reduced, and it was assumed that the powders were familiar.

[Measurement of fracture toughness]
About the sintered compact produced in Example 4, fracture toughness was measured based on JISR1607. The position of the boundary in the test piece is the same as in the above bending test. Moreover, the presser is matched with the position of the boundary between the second powder and the third powder. As a result, the fracture toughness was 4.3 MPa · m ^1/2 . As shown in Example 9 to be described later, this numerical value is the same as the fracture toughness of the sintered body produced without lamination, and it is understood that the fracture toughness is not reduced by the lamination.

[Measurement of shrinkage deformation during sintering]
In Example 4, with the calcined body produced by calcining at 1000 ° C. for 2 hours, the above-described test piece shown in FIGS. 1 and 2 was produced, and the test piece was fired at 1500 ° C. for 2 hours to deform. The amount (d / L × 100) was measured. The measuring method of the deformation was the same as the measuring method described above. Moreover, as a comparative example, the same test piece was produced also about the comparative example 1 and the comparative example 2 similarly to the bending test, and the deformation after sintering was measured. Table 8 shows the measurement results.

  In all the comparative examples, the deformation amount was 0.15 or more. On the other hand, in Example 4, the deformation amount can be 0.05 or less, and it can be seen that the deformation amount can be greatly suppressed as compared with the comparative example. From this, it is thought that the shrinkage deformation at the time of sintering can be suppressed by applying vibration to the composition during the lamination of powders having different compositions.

  Moreover, when the comparative example 1 and the comparative example 2 are compared, the deformation amount of the comparative example 1 is smaller. From this, it is thought that the direction which does not perform the press process after filling each layer can suppress the shrinkage deformation at the time of sintering more.

  Further, when comparing the two-layer laminate and the four-layer laminate, the deformation amount of the four-layer laminate is smaller than that of the two-layer laminate. From this, it is considered that shrinkage deformation can be further suppressed by increasing the number of layers.

[Measurement of chromaticity and color difference]
A single sintered body was prepared for each of the first powder, the second powder, the third powder, and the fourth powder in Examples 1 to 4, and the chromaticity according to the L ^* a ^* b ^* color system was measured. . The chromaticity was measured using a measuring apparatus CE100-DC / US manufactured by Olympus Corporation after processing the sintered body into a disk having a diameter of 14 mm and a thickness of 1.2 mm, and polishing both surfaces thereof. Moreover, based on the measurement result of chromaticity, the color difference ΔE ^* ab _1-3 between adjacent layers was calculated. Further, the color difference ΔE ^* ab ₄ between the first layer and the fourth layer was calculated. Then, (ΔE ^* ab ₁ + ΔE ^* ab ₂ + ΔE ^* ab ₃ ) −ΔE ^* ab ₄ was calculated. Tables 9-12 show chromaticity. Table 13 shows the color difference.

  The chromaticity of the sintered body of each powder is considered to represent the chromaticity of the color partially exhibited by the zirconia sintered body.

In the sintered body of the first layer of the four-layer laminate, L ^* was 58 to 73, a ^* was 0 to 8, and b ^* was 14 to 27. In the sintered body of the second layer, L ^* was 64-73, a ^* was 0-6, and b ^* was 16-22. In the sintered body of the third layer, L ^* was 70 to 78, a ^* was −2 to 2, and b ^* was 5 to 17. In the sintered body of the fourth layer, L ^* was 72 to 84, a ^* was −2 to 1, and b ^* was 4 to 15.

  The color difference between the sintered body of the first layer and the sintered body of the second layer was 7 to 14. The color difference between the sintered body of the second layer and the sintered body of the third layer was 10-18. The color difference between the third layer sintered body and the fourth layer sintered body was 4 to 9. The color difference between the sintered body of the first layer and the sintered body of the fourth layer was 28 to 36. Color difference between the sintered body of the first layer and the sintered body of the second layer, color difference between the sintered body of the second layer and the sintered body of the third layer, and sintering of the sintered body of the third layer and the fourth layer The value obtained by subtracting the color difference between the first layer sintered body and the fourth layer sintered body from the total body color difference was 1 or less.

[Example 5]
[Measurement of change in b ^* value]
For the mixed powder of zirconia and yttria (100% by mass), a low addition rate powder and a high addition rate powder in which a pigment is added at the addition rate shown in Table 14 are produced, and a composition is produced at the blending ratio shown in Table 15 Then, a sintered body was prepared in the same manner as in Examples 1 to 4, and the b ^* value of the L ^* a ^* b ^* color system was measured along the stacking direction (along the second direction Y in FIG. 1). Changes were measured. In FIG. 6, the schematic diagram and measurement result of the produced test piece are shown. The upper diagram of FIG. 6 is a schematic diagram of a test piece, showing dimensions and measurement directions. The lower diagram of FIG. 6 is a graph showing the measurement results. The sintered test piece was prepared to have a size of 20 mm × 20 mm × 1 mm after sintering. The first layer is a region filled with the first powder, and the fourth layer is a region filled with the fourth powder. b ^* value is measured by using a two-dimensional colorimeter RC-300 manufactured by Paparabo, placing a test piece in the center of an image of 29 mm × 22 mm size, and scanning in a direction perpendicular to the boundary surface of each layer. Performed at intervals of about 13 μm. The numerical value on the X axis in the lower graph of FIG. 6 indicates the number of measurement points. As Comparative Example 3, the change in the b ^* value was also measured for a sintered body produced by applying a press treatment each time the layers were filled without applying vibration when the powder of each layer was laminated. The composition and blending ratio of the low addition rate powder and the high addition rate powder in Comparative Example 3 are the same as in Example 5. In FIG. 7, the schematic diagram and measurement result of a test piece are shown.

From the graph of FIG. 7, it can be seen that the b ^* value tends to be flat in the central portion of each layer. In addition, at the boundary between the layers, a sudden step-like change in b ^* value is also observed. This is considered to be because the powder in each layer having a different pigment composition is sintered independently. According to this, a beautiful gradation is not formed in the appearance of the test piece of Comparative Example 3. On the other hand, looking at the graph of FIG. 6, the b ^* value tends to increase gradually even at the center of each layer. Further, no step-like change in b ^* value is observed at the boundary between the layers, and it is difficult to determine where the boundary is. In particular, the transition is linear at the boundary between the first layer and the second layer and the boundary between the third layer and the fourth layer. According to this, it turns out that the beautiful gradation is formed in the external appearance of the sintered compact of this invention. As a result, in the present invention, by applying vibration when filling the first to fourth powders, powder mixing occurs between adjacent layers in the vicinity of the boundary between the upper and lower layers, and the difference in the pigment content ratio between the adjacent layers occurs. This is thought to be due to the decrease in size. In addition, since the difference in pigment content is large between the second powder and the third powder, it is considered that the b ^* value in the graph also changes more rapidly than the other parts.

[Examples 6 to 15]
Based on the composition produced by laminating zirconia powders having different pigment compositions, a sintered body to be a dental prosthesis was produced. Moreover, the chromaticity of the sintered compact of each powder based on each layer was measured. Further, the bending strength, fracture toughness and monoclinic peak ratio after hydrothermal treatment were measured for the sintered body according to Example 9.

  First, a primary powder was produced in the same manner as in Examples 1 to 4. Next, the primary powder was divided into four parts. Let each powder be the 1st-4th powder. In Examples 6 to 15, pigments shown in Tables 6 to 16 below were added to each powder. The numerical value shown in the table is the addition rate with respect to the mixed powder (100% by mass) of zirconia and yttria. And the secondary powder of the 1st-4th powder was produced like Example 1-4 except having not produced the low addition rate powder and the high addition rate powder, and the addition rate of the pigment.

  Next, the molded object was produced by the method similar to Examples 1-4. Next, the compact was fired at 1000 ° C. for 2 hours to prepare a calcined body. Next, it was molded into a crown shape using a CAD / CAM system (Katana System, Kurarenoritake Dental Co., Ltd.). Next, the calcined body was fired at 1500 ° C. for 2 hours to produce a sintered body. The length of the sintered body in the stacking direction of the first to fourth powders was 8 mm.

  In any of the sintered bodies of Examples 6 to 16, a gradation changing from light yellow to yellowish white was formed from the region corresponding to the first layer of the composition to the region corresponding to the fourth layer. It had the same appearance as the teeth.

  In the same manner as in Examples 1 to 4, the chromaticity and color difference of the sintered bodies of the first powder, the second powder, the third powder, and the fourth powder were measured. Tables 26 to 35 show chromaticity. Tables 36 to 37 show the color differences.

  The chromaticity of each powder is considered to represent the chromaticity of each point of a zirconia sintered body produced from a laminate of a plurality of powders. The combination of the four sintered bodies of Example 9 exhibited a bright color as a whole. The combination of the four sintered bodies of Example 10 exhibited a dark color as a whole.

In the sintered body of the first layer, ^{L *} is from 58 to 76, ^{a *} is -2~8, ^{b *} was 5 to 27. In the sintered body of the second layer, L ^* was 66 to 81, a ^* was −2 to 6, and b ^* was 4 to 21. In the sintered body of the third layer, L ^* was 69 to 83, a ^* was −2 to 2, and b ^* was 3 to 17. In the sintered body of the fourth layer, L ^* was 71 to 84, a ^* was −2 to 1, and b ^* was 2 to 15.

  The color difference between the sintered body of the first layer and the sintered body of the second layer was 3-15. The color difference between the sintered body of the second layer and the sintered body of the third layer was 1 to 11. The color difference between the sintered body of the third layer and the sintered body of the fourth layer was 1 to 4. The color difference between adjacent layers tends to decrease from the first layer to the fourth layer. The color difference between the sintered body of the first layer and the sintered body of the fourth layer was 8 to 29. Color difference between the sintered body of the first layer and the sintered body of the second layer, color difference between the sintered body of the second layer and the sintered body of the third layer, and sintering of the sintered body of the third layer and the fourth layer The value obtained by subtracting the color difference between the first layer sintered body and the fourth layer sintered body from the total body color difference was 1 or less.

For each of the first powder, the second powder, the third powder, and the fourth powder in Example 9, single zirconia sintered bodies were prepared, and the bending strength, fracture toughness, and the peak ratio of monoclinic crystals after hydrothermal treatment were determined. It was measured. The measurement results are shown in Table 38. The bending strength of the zirconia sintered body was measured according to JIS R1601. The fracture toughness of the zirconia sintered body was measured according to JIS R1607. The hydrothermal treatment test conformed to ISO13356 under the conditions of 180 ° C., 1 MPa, and 5 hours. After the hydrothermal treatment test, the X-ray diffraction pattern of the zirconia sintered body was measured with CuKα rays, and the peak ratio of monoclinic crystals, that is, the degree of phase transition to monoclinic crystals was measured by the hydrothermal treatment test. All the sintered bodies had a bending strength of 1200 MPa or more, a fracture toughness of 4 MPa · m ^1/2 or more, and a monoclinic peak ratio of 1 or less. Since the zirconia sintered bodies in other examples have the same composition, it is considered that the same results can be obtained. The test results of bending strength and fracture toughness were the same as the numerical values when the test was performed with a load applied to the boundary of the laminate.

  Moreover, about the 2nd powder, the bending strength of the calcined body produced by baking at 1000 degreeC for 2 hours was also measured based on JISR1601. The bending strength of the calcined body of the second powder was 41 MPa. This numerical value was the same as the numerical value when the load was applied to the boundary of the laminate.

[Example 16]
In the above example, the yttria content was 4 mol% in terms of the total number of moles of zirconia and yttria. In Example 16, a 3 mol% sintered body was produced and the chromaticity was measured. The sintered body used for the measurement is the same as Example 4 shown in Tables 14 and 15 except for the yttria content. Table 39 shows the measurement results. Compared with the chromaticity shown in Table 12, when the yttria content was decreased, L ^* tended to decrease and a ^* and b ^* tended to increase.

  The zirconia sintered body of the present invention, and the composition and calcined body for the zirconia sintered body have been described based on the above embodiment, but are not limited to the above embodiment and are within the scope of the present invention. And various modifications to various disclosed elements (including each element of each claim, each element of each embodiment or example, each element of each drawing, etc.) based on the basic technical idea of the present invention. Needless to say, modifications and improvements can be included. Various combinations and replacements of various disclosed elements (including each element of each claim, each element of each embodiment or example, each element of each drawing, etc.) within the scope of the claims of the present invention. Or you can choose.

  Further problems, objects, and developments of the present invention will become apparent from the entire disclosure of the present invention including the claims.

  Regarding numerical ranges described in this document, any numerical value or small range included in the range should be construed as being specifically described even if there is no specific description.

A part or all of the above embodiment may be described as in the following supplementary notes, but is not limited to the following description.
[Appendix 1]
Containing a zirconia and a stabilizer that suppresses the phase transition of zirconia, forming a plurality of zirconia powders having different compositions;
Laminating the plurality of zirconia powders to form a zirconia composition;
Producing a zirconia sintered body obtained by sintering the zirconia composition;
In accordance with JISR1601, the load point of the three-point bending test is set to the position of the boundary with respect to the test piece of the sintered body in which the boundary of the plurality of zirconia powders crosses the test piece along the load application direction. A zirconia sintered body characterized in that the bending strength measured in accordance with the above is 1100 MPa or more.
[Appendix 2]
The zirconia sintered body according to the supplementary note, wherein the bending strength is 1200 MPa or more.
[Appendix 3]
When preparing a zirconia calcined body obtained by calcining the zirconia composition at 800 ° C. to 1200 ° C.,
According to JISR1601, the load point of the three-point bending test is set to the position of the boundary with respect to the test piece of the calcined body in which the boundary of the plurality of zirconia powders crosses the test piece along the load application direction. The bending strength measured in accordance with the zirconia powder is 90% or more of the bending strength of a zirconia calcined body obtained by calcining one of the zirconia powders at the same temperature as the calcining temperature of the test piece. The zirconia sintered body according to the supplementary note.
[Appendix 4]
The zirconia sintered body according to the supplementary note, wherein the plurality of zirconia powders contain a pigment and have different pigment contents.
[Appendix 5]
The zirconia sintered body according to the supplementary note, wherein each of the sintered bodies obtained by sintering the plurality of zirconia powders alone at 1500 ° C has a bending strength measured in accordance with JIS R1601 of 1100 MPa or more.
[Appendix 6]
Containing a zirconia and a stabilizer that suppresses the phase transition of zirconia, forming a plurality of zirconia powders having different compositions;
Laminating the plurality of zirconia powders to form a zirconia composition;
A zirconia calcined body obtained by calcining the composition at 800 ° C. to 1200 ° C.,
According to JISR1601, the load point of the three-point bending test is set to the position of the boundary with respect to the test piece of the calcined body in which the boundary of the plurality of zirconia powders crosses the test piece along the load application direction. The bending strength measured in accordance with the zirconia powder is 90% or more of the bending strength of a zirconia calcined body obtained by calcining one of the zirconia powders at the same temperature as the calcining temperature of the test piece. Zirconia calcined body.
[Appendix 7]
The zirconia calcined body as described in the supplementary note, wherein the plurality of zirconia powders contain a pigment and have different pigment contents.
[Appendix 8]
Zirconia, containing a stabilizer and a pigment that suppresses the phase transition of zirconia, and producing a plurality of lamination powders having different pigment content rates; and
Laminating a plurality of laminating powders in a mold,
In the laminating step, after the mold is filled with at least two powders for laminating, the mold is vibrated, and the method for producing a zirconia composition.
[Appendix 9]
The method for producing a zirconia composition according to the supplementary note, wherein in the laminating step, the die is vibrated each time the die is filled with one laminating powder.
[Appendix 10]
A step of producing a low addition rate powder and a high addition rate powder containing a stabilizer and a pigment for suppressing phase transition of zirconia and zirconia, and different content rates of the pigment;
A mixing step of mixing the low addition rate powder and the high addition rate powder to produce at least one lamination powder;
A laminating step of laminating at least two of the low addition rate powder, the high addition rate powder and the laminating powder in a mold;
The manufacturing method of the zirconia composition characterized by including.
[Appendix 11]
The method for producing a zirconia composition according to the supplementary note, wherein, in the laminating step, after the mold is filled with at least two powders, the mold is vibrated.
[Appendix 12]
In the mixing step, two or more laminating powders having different mixing ratios of the low addition rate powder and the high addition rate powder are produced,
The method for producing a zirconia composition according to the supplementary note, wherein in the laminating step, a plurality of powders are laminated so that the content of the low addition rate powder or the high addition rate powder changes in order.
[Appendix 13]
The method for producing a zirconia composition according to the supplementary note, wherein, in the laminating step, after the powder is filled into the mold, the upper surface of the powder is flattened.
[Appendix 14]
The method for producing a zirconia composition according to the supplementary note, wherein the powder is laminated so that the content of the pigment in the powder changes in order in the lamination step.
[Appendix 15]
A method for producing the zirconia composition according to the supplementary note,
Baking the composition at 800 ° C. to 1200 ° C .;
The manufacturing method of the zirconia calcined body characterized by including this.
[Appendix 16]
A method for producing the zirconia composition according to the supplementary note,
Baking the composition at 1400 ° C. to 1600 ° C .;
The manufacturing method of the zirconia sintered compact characterized by including this.
[Appendix 17]
A method for producing the zirconia calcined body described in the supplementary notes,
Firing the calcined body at 1400 ° C. to 1600 ° C .;
The manufacturing method of the zirconia sintered compact characterized by including this.

  The zirconia sintered body of the present invention includes dental materials such as prostheses, optical fiber connection parts such as ferrules and sleeves, various tools (for example, grinding balls and grinding tools), various parts (for example, screws, bolts and nuts). ), Various sensors, electronic parts, ornaments (for example, watch bands), and the like. When using a zirconia sintered body as a dental material, for example, coping, framework, crown, crown bridge, abutment, implant, implant screw, implant fixture, implant bridge, implant bar, bracket, denture base, inlay, It can be used for onlays, onlays, straightening wires, laminate veneers and the like.

10 Zirconia sintered body 20, 22 Calcined body 20a, 22a Bottom surface 21a, 21b First layer, second layer 23a-23d First to fourth layer 30 Grounding surface A-D First point to fourth point P One end Q The other end X 1st direction Y 2nd direction

According to the first aspect of the present invention, a zirconia composition containing yttria as a stabilizer for suppressing phase transition of zirconia and zirconia, forming a plurality of zirconia powders having different compositions, and laminating the plurality of zirconia powders. And a zirconia calcined body in a state of being produced by firing the zirconia composition at 800 ° C. to 1200 ° C. is provided. When the calcined body is molded into a rectangular parallelepiped shape with dimensions of 50 mm width × 10 mm height × 5 mm depth, the test piece has a bottom surface that is 50 mm wide × 5 mm depth by stacking zirconia powder. The formed boundary surface is parallel to the bottom surface, and when the test piece was baked at 1500 ° C. for 2 hours and placed with the bottom surface of the two bottom surfaces deformed into the concave surface (deformed into the concave surface) The maximum distance between the bottom surface and the ground contact surface / (distance between ground contact portions in the width direction) × 100 is 0.15 or less.

According to the 2nd viewpoint of this invention, the zirconia sintered compact which is the state which sintered the zirconia calcined body of this invention at 1400 degreeC-1600 degreeC is provided.

According to a fifth aspect of the present invention, a dental prosthesis a calcined body is in a state of being sintered after cutting of the present invention is provided.

Claims (23)

Containing a zirconia and a stabilizer that suppresses the phase transition of zirconia, forming a plurality of zirconia powders having different compositions;
Laminating the plurality of zirconia powders to form a zirconia composition;
A zirconia calcined body produced by firing the zirconia composition at 800 ° C. to 1200 ° C.,
When the calcined body is formed into a rectangular parallelepiped shape having dimensions of width 50 mm × height 10 mm × depth 5 mm, a test piece is used. The boundary surface formed by the lamination of is parallel to the bottom surface,
The test piece was fired at 1500 ° C. for 2 hours,
Of the two bottom surfaces, when placed with the bottom surface deformed into a concave surface,
A zirconia calcined body, wherein (maximum distance between the bottom surface deformed into a concave surface and the ground contact surface) / (distance between ground contact portions in the width direction) × 100 is 0.15 or less.   2. The zirconia calcination according to claim 1, wherein (maximum distance between the bottom surface deformed into a concave surface and the ground contact surface) / (distance between the ground contact portions in the width direction) × 100 is 0.1 or less. body.   3. The zirconia calcined body according to claim 1, wherein the plurality of zirconia powders contain a pigment and have different pigment contents.   A zirconia sintered body produced by a method including a step of sintering the zirconia calcined body according to any one of claims 1 to 3 at 1400 ° C to 1600 ° C. On a straight line extending in the first direction from one end to the other end,
The chromaticity (L ^* , a ^* , b ^* ) according to the L ^* a ^* b ^* color system of the first point in the section from one end to 25% of the total length is defined as (L1, a1, b1).
When the chromaticity (L ^* , a ^* , b ^* ) according to the L ^* a ^* b ^* color system of the second point in the section from the other end to 25% of the total length is (L2, a2, b2) ,
L1 is 58.0 or more and 76.0 or less,
a1 is -1.6 or more and 7.6 or less,
b1 is 5.5 or more and 26.7 or less,
L2 is 71.8 or more and 84.2 or less,
a2 is -2.1 or more and 1.8 or less,
b2 is 1.9 or more and 16.0 or less,
L1 <L2 and
a1> a2, and
b1> b2,
5. The zirconia sintered body according to claim 4, wherein an increasing / decreasing tendency of chromaticity due to the L ^* a ^* b ^* color system does not change from the first point toward the second point. On the straight line connecting the first point and the second point,
There is no section in which the L ^* value decreases by 1 or more from the first point toward the second point,
There is no section in which the a ^* value increases by 1 or more from the first point toward the second point,
6. The zirconia sintered body according to claim 5, wherein there is no section in which the b ^* value increases by 1 or more from the first point toward the second point. On the straight line connecting the first point to the second point, the chromaticity (L ^* , a ^* ) of the third point between the first point and the second point by the L ^* a ^* b ^* color system , B ^* ) is (L3, a3, b3),
L3 is 62.5 or more and 80.5 or less,
a3 is −1.8 or more and 5.5 or less,
b3 is 4.8 or more and 21.8 or less,
L1 <L3 <L2, and
a1>a3> a2,
b1>b3> b2.
The zirconia sintered body according to claim 5 or 6, characterized in that On the straight line connecting the first point to the second point, the chromaticity (L ^* , a ^* ) of the fourth point L ^* a ^* b ^* color system between the third point and the second point ^. , B ^* ) is (L4, a4, b4),
L4 is 69.1 or more and 82.3 or less,
a4 is -2.1 or more and 1.8 or less,
b4 is 3.5 or more and 16.2 or less,
L1 <L3 <L4 <L2,
a1>a3>a4> a2,
b1>b3>b4> b2.
The zirconia sintered body according to claim 7. The third point is at a distance of 45% of the total length from the one end,
The fourth point is at a distance of 55% of the total length from the one end,
The zirconia sintered body according to claim 8, wherein: In the first point, the third point, the fourth point, and the second point,
The difference between L ^* values at two adjacent points is ΔL ^* ,
The difference between a ^* values at two adjacent points is Δa ^* ,
The difference between b ^* values at two adjacent points is Δb ^* ,
When ΔE ^* ab is calculated from Equation 1 below,
ΔE ^* ab between the first point and the third point is 3.7 or more and 14.3 or less,
ΔE ^* ab between the third point and the fourth point is 1.8 or more and 10.5 or less,
ΔE ^* ab between the fourth point and the second point is 1.0 or more and 9.0 or less,
The zirconia sintered body according to claim 8 or 9, characterized in that.
[Formula 1]

On the straight line connecting the first point to the second point, the chromaticity (L ^* , a ^* ) of the third point between the first point and the second point by the L ^* a ^* b ^* color system , B ^* ) is (L3, a3, b3),
L3 is 69.1 or more and 82.3 or less,
a3 is -2.1 or more and 1.8 or less,
b3 is 3.5 or more and 16.2 or less,
L1 <L3 <L2, and
a1>a3> a2,
b1>b3> b2.
The zirconia sintered body according to claim 5 or 6, characterized in that The color changes in the first direction from one end to the other,
6. The zirconia sintered body according to claim 5, wherein an increasing / decreasing tendency of chromaticity due to the L ^* a ^* b ^* color system does not change on a straight line from the one end to the other end. On the straight line connecting the one end and the other end, the L ^* value tends to increase from the first point toward the second point, and the a ^* value and the b ^* value tend to decrease. The zirconia sintered body according to claim 12.   The zirconia sintered body according to any one of claims 5 to 13, wherein a distance from the one end to the other end is 5 mm to 18 mm.   The zirconia sintered body according to any one of claims 5 to 14, wherein the color does not change along a second direction orthogonal to the first direction. At two points on a straight line extending in the second direction,
The difference in L ^* value between the two points is ΔL ^* ,
The difference in a ^* value between the two points is Δa ^* ,
The difference in b ^* value between the two points is Δb ^* ,
When ΔE ^* ab is calculated from Equation 2 below,
The zirconia sintered body according to claim 15, wherein ΔE ^* ab is less than 1.
[Formula 2]

  The bending strength measured based on JISR1601 is 1000 MPa or more, The zirconia sintered compact as described in any one of Claims 5-16 characterized by the above-mentioned. The zirconia sintered body according to any one of claims 5 to 17, wherein the fracture toughness measured in accordance with JIS R1607 is 3.5 MPa · m ^1/2 or more.   In the X-ray diffraction pattern of the zirconia sintered body after the hydrothermal treatment test at 180 ° C. and 1 MPa for 5 hours, the height of the peak existing near the position where the [111] peak derived from tetragonal crystals with 2θ of around 30 ° occurs. The ratio of the height of the peak existing near the position where the [11-1] peak derived from the monoclinic crystal with 2θ of around 28 ° to 1 is 1 or less, The zirconia sintered body according to claim 1.   A zirconia composition comprising the calcined body according to any one of claims 1 to 3 by firing at 800 ° C to 1200 ° C.   It becomes a zirconia sintered compact as described in any one of Claims 5-19 by sintering at 1400 degreeC-1600 degreeC, The zirconia composition characterized by the above-mentioned.   A dental prosthesis characterized by being sintered after cutting the calcined body according to any one of claims 1 to 3.   The dental prosthesis according to claim 22, wherein the cutting is performed using a CAD / CAM system.

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