WO2023157923A1 - ジルコニアの仮焼体及び焼結体 - Google Patents

ジルコニアの仮焼体及び焼結体 Download PDF

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Publication number
WO2023157923A1
WO2023157923A1 PCT/JP2023/005481 JP2023005481W WO2023157923A1 WO 2023157923 A1 WO2023157923 A1 WO 2023157923A1 JP 2023005481 W JP2023005481 W JP 2023005481W WO 2023157923 A1 WO2023157923 A1 WO 2023157923A1
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WIPO (PCT)
Prior art keywords
zirconia
layer
less
region
sintered body
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
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PCT/JP2023/005481
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English (en)
French (fr)
Japanese (ja)
Inventor
祐貴 牛尾
翔 畦地
仁士 永山
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Tosoh Corp
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Tosoh Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Tosoh Corp filed Critical Tosoh Corp
Priority to US18/838,733 priority Critical patent/US20250197294A1/en
Priority to CN202380022180.0A priority patent/CN118742525A/zh
Priority to EP23756448.9A priority patent/EP4480935A4/en
Priority to KR1020247030480A priority patent/KR20240146063A/ko
Priority to JP2024501434A priority patent/JPWO2023157923A1/ja
Publication of WO2023157923A1 publication Critical patent/WO2023157923A1/ja
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C5/00—Filling or capping teeth
    • A61C5/70—Tooth crowns; Making thereof
    • A61C5/77—Methods or devices for making crowns
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    • C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
    • C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
    • C04B35/48—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on zirconium or hafnium oxides, zirconates, zircon or hafnates
    • C04B35/486—Fine ceramics
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    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C13/00—Dental prostheses; Making same
    • A61C13/0003—Making bridge-work, inlays, implants or the like
    • A61C13/0022—Blanks or green, unfinished dental restoration parts
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61C—DENTISTRY; APPARATUS OR METHODS FOR ORAL OR DENTAL HYGIENE
    • A61C13/00—Dental prostheses; Making same
    • A61C13/08—Artificial teeth; Making same
    • A61C13/083—Porcelain or ceramic teeth
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B32—LAYERED PRODUCTS
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    • C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C04B2235/9607—Thermal properties, e.g. thermal expansion coefficient
    • C04B2235/9615—Linear firing shrinkage
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C04B2235/9646—Optical properties
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C04B2235/9646—Optical properties
    • C04B2235/9653—Translucent or transparent ceramics other than alumina
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2235/00—Aspects relating to ceramic starting mixtures or sintered ceramic products
    • C04B2235/70—Aspects relating to sintered or melt-casted ceramic products
    • C04B2235/96—Properties of ceramic products, e.g. mechanical properties such as strength, toughness, wear resistance
    • C04B2235/9646—Optical properties
    • C04B2235/9661—Colour
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/30—Composition of layers of ceramic laminates or of ceramic or metallic articles to be joined by heating, e.g. Si substrates
    • C04B2237/32—Ceramic
    • C04B2237/34—Oxidic
    • C04B2237/345—Refractory metal oxides
    • C04B2237/348—Zirconia, hafnia, zirconates or hafnates
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
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    • C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/50—Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating
    • C04B2237/58—Forming a gradient in composition or in properties across the laminate or the joined articles
    • C—CHEMISTRY; METALLURGY
    • C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2237/00—Aspects relating to ceramic laminates or to joining of ceramic articles with other articles by heating
    • C04B2237/50—Processing aspects relating to ceramic laminates or to the joining of ceramic articles with other articles by heating
    • C04B2237/66—Forming laminates or joined articles showing high dimensional accuracy, e.g. indicated by the warpage

Definitions

  • the present disclosure relates to a zirconia calcined body and a zirconia sintered body, which are zirconia laminates.
  • a sintered body of zirconia (ZrO 2 ) is produced by molding, calcining and sintering raw material powder mainly containing zirconia.
  • the raw material powder is thermally shrunk and densified by heat treatment such as sintering and calcination, but the behavior during heat treatment varies depending on the characteristics of the raw material powder, particularly the composition of the raw material powder.
  • Zirconia accounts for most of the raw material powder. In spite of this, even if the raw material powders differ only in the additive content of less than 0.1% by mass, the thermal shrinkage behaviors of the two powders are significantly different. When a compact obtained by laminating raw material powders having such a slight difference in composition is heat-treated, problems such as peeling of a part of the layers or occurrence of distortion occur. The above mentioned drawbacks occur even with the same zirconia but with additives added to it. In order to heat-treat the compact without causing these problems, special adjustments and treatments have been required (eg, Patent Documents 1 and 2).
  • Patent Document 1 discloses that by coating the powder with a dopant to adjust the composition and thermal shrinkage behavior of the raw material powder and molding it, it is possible to obtain a sintered body composed of laminates of different colors without distortion. disclosed.
  • Patent Document 2 by applying vibration to form a boundary layer in which powders of upper and lower layers are mixed and laminating and molding, it consists of layers with different contents of coloring elements and has a change in color tone. It is disclosed that a sintered body consisting of a laminate can be obtained.
  • zirconia which accounts for the majority of the raw material powder, has the same composition, and these laminates have the same texture mainly due to the translucency of zirconia. . Therefore, a texture different from that of a natural tooth, which has a texture derived from a change in translucency, was provided.
  • Patent Document 3 discloses a laminate obtained by laminating a plurality of zirconia composition layers having different chemical compositions.
  • Patent Literature 3 layers in which the amounts of yttrium and coloring elements are changed stepwise are laminated from the bottom layer to the top layer so that the color tone and transmittance are gradually changed.
  • layers with different compositions are stacked so that the color tone and transmittance gradually change, the composition of the bottom layer and the top layer will differ greatly.
  • the shrinkage rate of the layers varies greatly.
  • a molded body having such a large difference in contraction rate between the lowermost layer and the uppermost layer is heat-treated, a calcined body or a sintered body that warps greatly toward the side with a larger contraction rate is obtained.
  • the present disclosure provides a sintered body having translucency and color gradation that can give an impression close to natural teeth when viewed visually, and a calcined body that provides such a sintered body,
  • An object of the present invention is to provide at least one of a zirconia calcined body and a sintered body in which warpage is suppressed even after heat treatment such as calcination and calcination.
  • Another object of the present disclosure is to provide at least one of a calcined body and a sintered body suitable as a dental prosthetic material, and a method for producing them.
  • the present inventors have found the relationship between the content of the stabilizing element in the zirconia composition contained in the bottom layer and the content of the stabilizing element in the zirconia composition contained in the top layer, or By focusing on the relationship between the shrinkage rate and the shrinkage rate of the uppermost layer and controlling them to a specific relationship, despite having a laminated structure that gradually changes the translucency and color tone like natural teeth. , a sintered body with suppressed warpage and a calcined body that gives such a sintered body can be obtained.
  • a sintered body of zirconia contains (i) stabilizing element-containing zirconia, or (ii) stabilizing element-containing zirconia and a coloring element
  • the sintered body has three or more regions laminated in layers, and the content of at least one of the stabilizing element and the coloring element is different in two adjacent regions among the regions. , Among the laminated regions, the content of the stabilizing element contained in the first region located at one end and the content of the stabilizing element contained in the second region located at the other end difference is 2.0 mol% or less.
  • the third region includes two or more regions, and from the first region to the third region or from the second region to the third region along the stacking direction
  • a sintered body of zirconia, The zirconia contains (i) stabilizing element-containing zirconia, or (ii) stabilizing element-containing zirconia and a coloring element,
  • the sintered body has three or more regions laminated in layers, and the content of at least one of the stabilizing element and the coloring element is different in two adjacent regions among the regions.
  • the third region includes two or more regions, and from the first region to the third region or from the second region to the third region along the stacking direction.
  • a calcined body of a zirconia composition contains (iii) a stabilizing element-containing zirconia composition having a necking structure, or (iv) a zirconia composition containing a stabilizing element-containing zirconia having a necking structure and a coloring element. death,
  • the calcined body has three or more regions laminated in layers, and the content of at least one of the stabilizing element and the coloring element is different in two adjacent regions among the regions. , Among the laminated regions, the content of the stabilizing element contained in the first region located at one end and the content of the stabilizing element contained in the second region located at the other end difference is 2.0 mol% or less, the calcined body.
  • the third region includes two or more regions, and from the first region to the third region or from the second region to the third region along the stacking direction
  • a calcined body of a zirconia composition contains (iii) a stabilizing element-containing zirconia composition having a necking structure, or (iv) a zirconia composition containing a stabilizing element-containing zirconia having a necking structure and a coloring element.
  • the calcined body has three or more regions laminated in layers, and the content of at least one of the stabilizing element and the coloring element is different in two adjacent regions among the regions. , Among the laminated regions, the difference (shrinkage rate difference) is 0.4% or less.
  • the calcined body according to [10] wherein the third region layered on the first region and the second region includes one or more regions.
  • the third region includes two or more regions, and from the first region to the third region or from the second region to the third region along the stacking direction
  • the calcined body according to [11] wherein the color tone does not change with increasing or decreasing.
  • [13] The method for producing a sintered body according to any one of [1] to [6], Sintering at 1200° C. or higher and 1600° C. or lower a molded body in which three or more layers of a powder composition layer composed of a zirconia raw material powder containing a stabilizing element-containing zirconia and, if a coloring element is contained, a coloring element are laminated.
  • a method for producing a sintered body comprising the step of: [14] The method for producing a sintered body according to any one of [1] to [6], calcining at 800° C. or more and less than 1200° C.
  • a molded body having three or more layers of powder composition layers composed of zirconia raw material powders containing stabilizing element-containing zirconia and, if a coloring element is contained, a coloring element; and sintering the calcined body at 1200° C. or higher and 1600° C. or lower.
  • a method for producing a calcined body comprising the step of: [16] A dental material containing the sintered body according to any one of [1] to [6]. [17] A dental material comprising the calcined body according to any one of [7] to [12].
  • a sintered body having translucency and color gradation that can give an impression close to natural teeth when viewed visually and a calcined body that provides such a sintered body
  • a zirconia calcined body and a sintered body in which warpage is suppressed even after heat treatment such as calcination and calcination.
  • Schematic diagram showing a cross section of a sintered body having a structure in which three zirconia layers are laminated Schematic diagram showing a cross section of a sintered body having a structure in which four zirconia layers are laminated
  • Schematic diagram explaining the molding process of uniaxial press molding Schematic diagram explaining the molding process of CIP processing
  • Schematic diagram showing how to measure warpage Schematic diagram showing how to measure three-point bending strength
  • Schematic diagram for explaining the molding process of uniaxial press molding when producing a laminate in the example Schematic diagram for explaining the forming process of the CIP treatment when producing the laminate in the example.
  • a zirconia sintered body and a calcined body according to one embodiment of the present disclosure will be described in detail below. Note that the description of the constituent elements described below is an example for describing one mode of the present disclosure, and the present disclosure is not limited to these contents.
  • the laminate may include any form of a sintered body, a calcined body, and a molded body.
  • the laminate of the present embodiment is a sintered body as a dental prosthesis, and a calcined body as a precursor thereof.
  • the sintered body when the laminate is a sintered body, is "a stabilizing element-containing zirconia that is zirconia in which a stabilizing element is dissolved, and a coloring element if it contains a coloring element.
  • the calcined body has a structure in which regions made of zirconia containing a and, if a coloring element is contained, a zirconia composition containing a coloring element" has a structure in which layers are laminated, and when the laminate is a molded article, It has a structure in which regions composed of "a powder composition containing a stabilizing element-containing zirconia and, when a coloring element is contained, a powder composition containing a coloring element" are laminated in layers.
  • the transparency and color tone can be changed to form gradation of translucency and color tone.
  • the region is “laminated in layers”, which means that the region made of zirconia with different compositions due to different contents of stabilizing elements and coloring elements is a sintered body or multiple regions in the calcined body, and these multiple regions exist along the stacking direction.
  • the present disclosure does not define a "layer lamination" state in which the interface between layers can be visually recognized and the lamination state of each layer can be confirmed.
  • it is not required to visually recognize the lamination state of each layer, and even if there is no visible interface, a plurality of regions with different compositions are visible. , exists along one direction, it can be said that the region referred to in the present disclosure corresponds to “laminated in layers”.
  • the calcined body and the sintered body are formed by laminating a powder composition layer made of a zirconia raw material powder containing a stabilizing element-containing zirconia and a coloring element if it contains a coloring element, and then molding. It is obtained by calcining or sintering the compact after producing the compact.
  • a "region" in a sintered body or a calcined body is formed by calcining or sintering each powder composition layer in the molded body. That is, each "region" in the sintered body or the calcined body substantially corresponds to each powder composition layer in the molded body.
  • the lower limit is 1 mm or more, more preferably 2 mm or more, while the upper limit is 20 mm or less, more preferably 15 mm or less.
  • Preferred embodiments of the thickness of the layer are, for example, 1 mm to 20 mm, 1 mm to 15 mm, 2 mm to 20 mm, or 2 mm to 15 mm.
  • the sintered body according to this embodiment is A sintered body of zirconia,
  • the zirconia includes (i) zirconia containing a stabilizing element, or (ii) zirconia containing a stabilizing element and a coloring element.
  • the zirconia contains (i) stabilizing element-containing zirconia.
  • Stabilizing element-containing zirconia may further contain a coloring element, in which case the zirconia contains (ii) stabilizing element-containing zirconia and coloring element-containing zirconia.
  • the sintered body has three or more regions laminated in layers, and the contents of at least one of the stabilizing element and the coloring element are different in two adjacent regions among the regions.
  • a sintered body of zirconia includes (i) zirconia containing a stabilizing element, or (ii) zirconia containing a stabilizing element and a coloring element.
  • the sintered body has three or more regions laminated in layers, and the contents of at least one of the stabilizing element and the coloring element are different in two adjacent regions among the regions. and The difference (shrinkage index difference) is 0.4% or less.
  • a sintered body is a laminate composed of a sintered structure.
  • the sintered structure is a structure mainly composed of zirconia in the later stage of sintering.
  • the sintered body of the present embodiment includes a zirconia layer made of zirconia containing a stabilizing element, or a zirconia layer made of zirconia containing zirconia containing a stabilizing element and a coloring element when a coloring element is contained (hereinafter referred to as these
  • the zirconia layers of are also simply referred to as “zirconia layers”.).
  • the zirconia layer consists mainly of crystal grains of zirconia containing stabilizing elements.
  • the sintered body of the present embodiment can be regarded as a zirconia layer made of zirconia crystal grains containing a stabilizing element, or when a coloring element is contained, the zirconia crystal grains containing a stabilizing element It can also be regarded as a laminate having three or more layers of zirconia and a zirconia layer containing a coloring element. In this specification, the zirconia layer is also referred to as a sintered body layer.
  • FIG. 1 is a schematic diagram showing an example of the laminated structure of the sintered body of this embodiment.
  • FIG. 1 shows a cross section of a sintered body (100) having a structure in which three zirconia layers are laminated.
  • Each of the three layers in FIG. 1 corresponds to each "region" described in this disclosure.
  • the Y-axis direction indicates the stacking direction
  • the X-axis direction indicates the direction in which each layer spreads (hereinafter, also referred to as "horizontal direction").
  • the sintered body (100) includes a first zirconia layer (hereinafter also referred to as "first layer”) (11) and a second zirconia layer (hereinafter also referred to as “second layer”) (12). and a third zirconia layer (hereinafter also referred to as “third layer”) (13), and the first layer (11), the third layer (13), and the second layer (12 ) and are stacked in this order.
  • first layer first layer
  • second layer second zirconia layer
  • third layer a third zirconia layer
  • Each layer (each region) indicated by the first layer (11), the third layer (13) and the second layer (12) has the same composition of zirconia in each layer (region), but is adjacent to each other. The composition of zirconia between the layers is different.
  • Each layer (each region) of the first layer (11), the third layer (13), and the second layer (12) may further contain a coloring element in addition to the stabilizing element-containing zirconia.
  • the coloring element may be contained in all three layers of the first layer (11), the third layer (13), and the second layer (12), or may be contained in only some of them. good.
  • the first layer (11), the third layer (13), and the second layer (12) does not contain a coloring element, the first layer (11), the third layer (13), Each layer (each region) indicated by the second layer (12) differs from the adjacent layer (adjacent region) in the content of the stabilizing element.
  • the coloring element is contained in all or part of the first layer (11), the third layer (13), and the second layer (12), the first layer (11), the Each layer (each region) indicated by the third layer (13) and the second layer (12) differs from the adjacent layer (adjacent region) in the content of at least one of the stabilizing element and the coloring element. .
  • the sintered body of the present embodiment will be specifically described below with reference to FIG. 1, taking as an example the case where the coloring element is contained in the three zirconia layers shown in FIG.
  • the sintered body (100) includes a first zirconia layer (first layer) (11) containing zirconia containing a stabilizing element and a coloring element, and a first zirconia layer (11) containing zirconia containing a stabilizing element and a coloring element.
  • 2 zirconia layer (second layer) (12) and a third zirconia layer (third layer) (13) containing a stabilizing element-containing zirconia and a coloring element, and the first layer (11), a third layer (13), and a second layer (12) are laminated in this order.
  • Each layer (each region) indicated by the first layer (11), the third layer (13), and the second layer (12) has the same zirconia composition within each layer (region). Therefore, along the X direction in FIG. 1, no change in translucency or color tone due to the difference in content of at least one of the stabilizing element and the coloring element is observed.
  • each layer (each region) represented by the first layer (11), the third layer (13), and the second layer (12) has different zirconia compositions in adjacent layers (adjacent regions).
  • the content of at least one of the stabilizing element and the coloring element is different between adjacent layers (adjacent regions).
  • "Adjacent layers have different zirconia compositions” means, for example, that the content of the stabilizing element in the adjacent layers does not change and only the content of the coloring element changes, or that the content of the coloring element in the layers adjacent to each other changes is the same, but only the content of the stabilizing element is changed, or the content of the stabilizing element and the content of the coloring element are changed in adjacent layers. In the example of FIG.
  • the content of at least one of the stabilizing element and the coloring element contained in the zirconia layer of the third layer (13) is the same as that of the stabilizing element contained in the adjacent zirconia layer of the first layer (11). different from the content of at least one of the stabilizing element and the coloring element, and different from the content of at least one of the stabilizing element and the coloring element contained in the zirconia layer of the adjacent second layer (12).
  • Each layer (each region) represented by the first layer (11), the third layer (13), and the second layer (12) is composed of adjacent layers (adjacent regions) and at least one of a stabilizing element and a coloring element.
  • the adjacent layers have different contents of the stabilizing element and the coloring element.
  • the content of the stabilizing element and the coloring element contained in the zirconia layer of the third layer (13) is the content of the stabilizing element and the content of the coloring element contained in the adjacent zirconia layer of the first layer (11). It is preferably different from the content of the stabilizing element and the content of the coloring element contained in the adjacent zirconia layer of the second layer (12).
  • the stabilizing element and the coloring element are arranged along the Y direction in FIG. It is possible to form a sintered body in which a change in translucency and color tone based on the difference in the content of is visible.
  • the sintered body (100) of FIG. 1 the first layer and the third layer, or the third layer and the second layer are in contact with each other through the interface.
  • the sintered body of the present embodiment may be laminated without a visible interface, and the interface between layers is not limited to being linear.
  • the sintered body of the present embodiment may have a structure in which three or more zirconia layers containing a stabilizing element-containing zirconia and, if a coloring element is contained, a coloring element are laminated. It may have a structure in which one or more layers, or five or more layers are laminated. By increasing the number of layers, the sintered body becomes a laminate in which fine changes in texture can be visually recognized. When the texture is more similar to that of a natural tooth, the sintered body of the present embodiment has 3 to 10 zirconia layers, further 3 to 6 layers, further 4 to 7 layers, or Furthermore, a structure in which 4 to 6 layers are laminated can be exemplified.
  • a zirconia layer other than the first layer and the second layer may be provided between the first layer and the second layer, and the sintered body of the present embodiment has a plurality of An intermediate layer may be included. That is, the third region (intermediate layer) layered between the first region and the second region may include not only one region but also two or more regions.
  • the order of stacking the intermediate layers is arbitrary, but for example, a plurality of intermediate layers (the intermediate layer adjacent to the first layer is the "third layer", the second or more intermediate layers adjacent to the third layer Also referred to as “fourth layer”, “fifth layer”, etc.) in the stacking direction from the intermediate layer, the sintered body of the present embodiment contains at least one of a stabilizing element and a coloring element in the stacking direction. It is preferable to have a structure in which the zirconia layers are stacked so that the change in the amount is constant, that is, to have a structure in which the zirconia layers are stacked so that the change in amount is increased (or decreased).
  • the structure in which the intermediate layer is sandwiched between the first layer and the second layer is a structure in which the intermediate layer is positioned between the first layer and the second layer in the stacking direction,
  • An example in which the first layer, the third layer, and the second layer are laminated in this order is as described with reference to FIG. A case where the intermediate layer has a plurality of layers will be described below with reference to FIG.
  • the first, second, third, etc. are numbers given for convenience of explanation, and are limited to cases where the order of lamination and the lamination state are shown in FIGS. not to be
  • FIG. 2 is a schematic diagram showing another example of the structure of the sintered body of this embodiment.
  • FIG. 2 shows a cross section of a sintered body (200) having a structure in which four zirconia layers are laminated.
  • the sintered body (200) has a structure in which a third layer (23) and a fourth layer (24), which are intermediate layers, are laminated in addition to the first layer (21) and the second layer (22). ing.
  • Each layer (each region) of the first layer (21), the third layer (23), the fourth layer (24), and the second layer (22) further contains a coloring element in addition to the stabilizing element-containing zirconia. may be contained.
  • the coloring element may be contained in all four layers of the first layer (21), the third layer (23), the fourth layer (24), and the second layer (22), or may be contained in some of them. may be contained only in When each layer of the first layer (21), the third layer (23), the fourth layer (24), and the second layer (22) does not contain a coloring element, the first layer (21), Each layer (each region) indicated by the third layer (23), the fourth layer (24), and the second layer (22) has a different stabilizing element content from the adjacent layers (adjacent regions). .
  • first layer (21), third layer (23), fourth layer (24), and second layer (22) contains a coloring element
  • first layer (21), the third layer (23), the fourth layer (24), the second layer (22) each layer (each region) is connected to the adjacent layer (adjacent region) and the stabilizing The content of at least one of the element and the coloring element is different from each other.
  • the sintered body (200) includes a first zirconia layer (first layer) (21) containing stabilizing element-containing zirconia and a coloring element, and a stabilizing element-containing zirconia and a coloring element.
  • first layer first layer
  • second layer 22
  • stabilizing element-containing zirconia 2
  • third zirconia layer 3rd layer
  • fourth zirconia layer fourth layer
  • Each layer (each region) represented by the first layer (21), the third layer (23), the fourth layer (24), and the second layer (22) has zirconia composition is different. That is, the content of at least one of the stabilizing element and the coloring element is different between adjacent layers (adjacent regions).
  • the content of at least one of the stabilizing element and the coloring element contained in the zirconia layer of the third layer (23) is equal to the content of at least one of the stabilizing element and the coloring element contained in the adjacent zirconia layer of the first layer (21) It differs from the above content and differs from the content of at least one of the stabilizing element and the coloring element contained in the adjacent zirconia layer of the fourth layer (24).
  • the content of at least one of the stabilizing element and the coloring element contained in the zirconia layer of the fourth layer (24) is equal to that of the stabilizing element and the coloring element contained in the adjacent zirconia layer of the third layer (23). It is different from the content of at least one of them and is also different from the content of at least one of the stabilizing element and the coloring element contained in the zirconia layer of the adjacent second layer (22).
  • the contents of at least one of the element and the coloring element are different, in order to obtain the desired change in translucency and color tone
  • the adjacent layers (adjacent regions) and the contents of the stabilizing element and the coloring element are preferably different. That is, the content of the stabilizing element and the coloring element contained in the zirconia layer of the third layer (23) is the content of the stabilizing element and the content of the coloring element contained in the adjacent zirconia layer of the first layer (21).
  • the content of the stabilizing element and the content of the coloring element contained in the adjacent zirconia layer of the fourth layer (24) is the content of the stabilizing element and the content of the coloring element contained in the adjacent zirconia layer of the third layer (23). It is preferably different from the content of the stabilizing element and the content of the coloring element contained in the zirconia layer of the adjacent second layer (22).
  • the zirconia layers are laminated so that the tendency of at least one of the light transmittance and the color tone does not change along the lamination direction.
  • the zirconia layers are laminated so that the increase or decrease tendency of at least one of the translucency and color tone does not change along the lamination direction.
  • gradation of translucency and color tone can be formed based on the content difference of at least one of the stabilizing element and the coloring element.
  • the stabilizing element and the coloring element are formed based on the content difference of at least one of the stabilizing element and the coloring element.
  • one of the stacked layers The layer located at the end (that is, one region that is the top layer or the bottom layer in the stacking direction) and the layer located at the other end (that is, the other region that is the top layer or the bottom layer in the stacking direction)
  • the amount of stabilizing element or shrinkage of the layer should be close to each other.
  • the present disclosure in the case of a sintered body in which four or more zirconia layers are laminated, either the layer positioned at one end or the layer positioned at the other end is transparent along the lamination direction.
  • the increase/decrease trend of at least one of lightness and color tone may be reversed with respect to the increase/decrease trend of other layers.
  • the present disclosure includes such forms. A more specific description of such a form is as shown in (a) and (b) below. (a) When the third region includes two or more regions, the increasing or decreasing tendency of at least one of the translucency and color tone does not change along the stacking direction from the first region to the third region can be the composition of the layer without changing. That is, in FIG.
  • the composition of the layer can be such that the increasing or decreasing tendency of at least one of lightness and color tone does not change. As a result, translucency and color gradation close to those of natural teeth can be formed.
  • a second layer (corresponding to the second region) (22) is laminated on the fourth layer (24).
  • the second layer (22) is a layer that exhibits a value close to the content of the stabilizing element in the first layer or a value close to the shrinkage rate of the first layer.
  • the first layer (21) to the fourth layer (24) In this way, by laminating the second layer (22) close to at least one of the stabilizing element content and shrinkage rate of the first layer, in some cases, the first layer (21) to the fourth layer (24) In some cases, the direction of increase or decrease of at least one of the translucency and color tone that appeared over the period of time is reversed. However, in such a case, for example, when processing into the shape of a dental product such as a crown shape, adjustment may be made so that the crown shape is processed within the layered range in which the desired gradation is formed. (b) When the third region includes two or more regions, a layer in which at least one of translucency and color tone does not change along the stacking direction from the second region to the third region composition. That is, in FIG.
  • the composition of the layer can be such that the increasing or decreasing tendency of at least one of lightness and color tone does not change. As a result, translucency and color gradation close to those of natural teeth can be formed.
  • a first layer (corresponding to the first region) (21) is laminated under the third layer (23). Since the first layer (21) is a layer that exhibits a value close to the content of the stabilizing element in the second layer or a value close to the shrinkage rate of the second layer, the stabilization of the second layer is performed in this way.
  • the translucency and color tone that appeared from the second layer (22) to the third layer (23) The direction of increase or decrease of at least one of may be reversed.
  • adjustment may be made so that the crown shape is processed within the layered range in which the desired gradation is formed.
  • Preferred embodiments of the sintered body of the present disclosure include a sintered body described in the following mode (A) and a sintered body described in the following mode (B).
  • the sintered body of the present embodiment has translucency and color gradation similar to those of natural teeth, while suppressing warpage and causing little deformation.
  • the relationship between the first region (eg, the first layer (11)) located at one end and the second region (eg, the second layer (12)) located at the other end
  • the warping of the sintered body can be effectively suppressed. Therefore, a zirconia layer having an arbitrary composition can be laminated for each layer of the intermediate layer disposed between the first layer (11) and the second layer (12).
  • the difference between the content of the stabilizing element contained in the first region and the content of the stabilizing element contained in the second region is 2.0 mol% or less, It is preferably 1.8 mol % or less, 1.5 mol % or less, or 0.8 mol % or less.
  • the difference between the content of the stabilizing element contained in the first region and the content of the stabilizing element contained in the second region is preferably small. .1 mol % or more, or 0.3 mol % or more.
  • the difference may be 0 mol % or more and 2.0 mol % or less, 0 mol % or more and 1.5 mol % or less, 0 mol % or more and 1.8 mol % or less, or 0 mol % or more and 1.5 mol % or less.
  • the content of the stabilizing element in each region is the molar ratio of the stabilizing element converted to oxide with respect to the total of the stabilizing element converted to zirconia and oxide.
  • the oxide conversion of the stabilizing element is Y2O3 for yttrium, CaO for calcium, MgO for magnesium, CeO2 for cerium, Pr6O11 for praseodymium , Nd2O3 for neodymium, Tb4O7 for terbium , Erbium may be Er 2 O 3 and ytterbium may be Yb 2 O 3 .
  • the content (mol%) of stabilizing elements is (Y 2 O 3 +Er 2 O 3 )/(ZrO 2 +Y 2 O 3 +Er 2 O 3 ) ⁇ 100. requested from.
  • the shrinkage rate of the sintered body in the first region located at one end of the stacked regions and the sintered body in the second region located at the other end is 0.4% or less.
  • the form (B) will be described with reference to FIG. Along the Y-axis direction (stacking direction) in FIG.
  • the shrinkage rate of the sintered body with the second layer (12)) is set to a value close to that of the second layer (12) (specifically, 0.4% or less).
  • the sintered body of the present embodiment has translucency and color gradation similar to those of natural teeth, while suppressing warpage and causing little deformation.
  • the relationship between the first region (eg, the first layer (11)) located at one end and the second region (eg, the second layer (12)) located at the other end can be adjusted by adjusting the shrinkage ratio of the regions (layers) located at both ends. Therefore, a zirconia layer having an arbitrary composition can be laminated for each layer of the intermediate layer disposed between the first layer (11) and the second layer (12).
  • the difference between the shrinkage rate of the sintered body in the first region and the shrinkage rate of the sintered body in the second region is 0.4% or less, and 0.36% Below, it is preferably 0.3% or less or 0.2% or less.
  • the difference between the shrinkage rate of the sintered body in the first region and the shrinkage rate of the sintered body in the second region is preferably small, for example, 0% or more, more than 0%, or 0.01% or more. Alternatively, it may be 0.02% or more. Even if the difference is 0% or more and 0.4% or less, more than 0% and 0.36% or less, 0.0.01% or more and 0.2% or less, or 0.02% or more and 0.2% or less good.
  • the shrinkage ratios of the first region (eg, the first layer (11)) located at one end and the second region (eg, the second layer (12)) located at the other end are as follows.
  • a zirconia raw material powder having the same composition as the first layer (11) and the second layer (12) is filled in a mold, uniaxially pressurized (hereinafter also referred to as “uniaxial press”), and cold isostatic press (hereinafter referred to as cold isostatic press). , also referred to as “CIP”) to form a powder composition layer that is a sample for shrinkage measurement.
  • the powder composition layer is calcined at 800° C.
  • the shrinkage rate of the zirconia layer is determined by the method described in the section [Method for evaluating shrinkage rate] below.
  • a sample for shrinkage measurement may be prepared under the following conditions.
  • Mold diameter ⁇ 25mm
  • Powder mass 4g
  • Molding pressure Uniaxial press molding: 49 MPa +
  • CIP treatment 196 MPa
  • Molding process Put the powder to be evaluated into the mold ⁇ leveling ⁇ uniaxial press molding ⁇ CIP processing
  • FIG. 3 schematically shows a molding process of uniaxial press molding in the preparation of the above sample
  • FIG. 4 schematically shows a molding process of CIP treatment.
  • the powder (31) is put into the mold (32) ⁇
  • the powder is leveled ⁇
  • the uniaxial press molding (33) is performed to press the powder.
  • the uniaxially pressed powder (41) is placed in a high-pressure container, the high-pressure container is filled with a solvent (42) such as water, and the powder is isotropically pressurized by water pressure (CIP treatment). It is shown.
  • the obtained shrinkage measurement sample is calcined under the following conditions and then sintered.
  • Calcination is performed at 800° C. or more and less than 1200° C., and sintering is performed at 1200° C. or more and 1600° C. or less. More detailed conditions can be selected as appropriate.
  • calcination and then sintering may be performed under the following conditions. Calcination: 15°C/hour from room temperature to 300°C, held at 300°C for 5 hours, 15°C/hour from 300°C to 700°C, held at 700°C for 1 hour, 50°C/hour from 700°C to 1000°C, 1000 C. for 2 hours and then cooled in the furnace. Sintering: from room temperature to 1500°C at 100°C/hour, held at 1500°C for 2 hours, and then cooled in the furnace.
  • the contraction rate is measured for the sintered body of the shrinkage rate measurement sample obtained as described above.
  • a caliper is used to measure the diameter of the sintered body of the sample for shrinkage rate measurement (hereinafter also referred to as "sample diameter").
  • the diameter of the sample may be obtained by measuring the diameter of the shrinkage measurement sample at four points each using a vernier caliper, and taking the average value of the measured values as the sample diameter.
  • the shrinkage ratio is calculated from the following formula (1).
  • the sintered body of the present embodiment is composed of a zirconia layer containing a stabilizing element-containing zirconia and a coloring element when the coloring element is contained.
  • the zirconia layer is a layer containing zirconia as a main component, and the zirconia is zirconia containing a stabilizing element.
  • the sintered body and the zirconia layer (sintered body layer) of the present embodiment may contain not only the stabilizing element zirconia and the coloring element, but also unavoidable impurities such as hafnia (HfO 2 ).
  • hafnia as an unavoidable impurity varies greatly depending on the raw material ore and production method, but can be exemplified as 2.0% by mass or less.
  • calculation of values related to composition such as calculation of content and density, may be performed by regarding hafnia as zirconia (ZrO 2 ).
  • the zirconia is preferably zirconia obtained by sintering zirconia obtained by heat-treating a zirconia sol, and zirconia obtained by heat-treating a zirconia sol obtained by hydrolysis of a zirconium compound.
  • Zirconia in a sintered state is more preferred, and zirconia in a sintered state of zirconia obtained by heat-treating a zirconia sol obtained by hydrolyzing zirconium oxychloride is even more preferred.
  • the zirconia contained in the zirconia layer is sintered zirconia, that is, zirconia crystal grains.
  • the stabilizing element may be any element that has a function of suppressing the phase transition of zirconia.
  • the stabilizing element is an element that does not have the function of coloring zirconia but has the function of suppressing phase transition (hereinafter also referred to as "non-coloring stabilizing element”), and has the function of coloring zirconia,
  • At least one of elements having a function of suppressing phase transition (hereinafter also referred to as "coloring stabilizing element”), may be a non-coloring stabilizing element and a coloring stabilizing element, and at least a non-coloring stabilizing element It is preferable to contain a chemical element.
  • Specific stabilizing elements include yttrium (Y), calcium (Ca), magnesium (Mg), cerium (Ce), praseodymium (Pr), neodymium (Nd), terbium (Tb), erbium (Er) and ytterbium ( One or more selected from the group Yb) can be exemplified.
  • the non-color stabilizing element one or more selected from the group of yttrium, calcium, magnesium and cerium can be exemplified, preferably at least one of yttrium and cerium, more preferably yttrium.
  • the coloring stabilizing element examples include one or more selected from the group consisting of praseodymium, neodymium, terbium, erbium and ytterbium, preferably at least one of terbium and erbium.
  • Preferred stabilizing elements are one or more selected from the group of yttrium, terbium and erbium, further yttrium, terbium and erbium, moreover at least one of terbium and erbium and yttrium, moreover are erbium and yttrium, or even yttrium.
  • the stabilizing element is contained in zirconia and dissolved in zirconia.
  • the sintered body of the present embodiment does not contain an undissolved stabilizing element, that is, does not contain a stabilizing element that is not dissolved in zirconia.
  • "not containing an undissolved stabilizing element” means that no XRD peak derived from the stabilizing element is confirmed in the XRD measurement and XRD pattern analysis described later. It is permissible to contain an undissolved stabilizing element as long as the XRD peak derived from is not confirmed.
  • the stabilizing element content of the stabilizing element-containing zirconia contained in each layer is, for example, a lower limit of 1.5 mol% or more and 2.5 mol% or more. , 3.0 mol % or more, 3.5 mol % or more, or 4.0 mol % or more, and the upper limit is 7.0 mol % or less, 6.0 mol % or less, or 5.0 mol % or less. Any combination of these upper and lower limits may be used.
  • the stabilizing element content of the stabilizing element-containing zirconia contained in each layer (corresponding to each region) of the present embodiment is 1.5 mol% or more and 7.0 mol% or less, and 2.5 mol% or more and 6.0 mol%. or less, or 3.0 mol % or more and 6.0 mol % or less.
  • the content of the stabilizing element of zirconia for example, preferably has a lower limit of 1.5 mol % or more or 2.5 mol % or more, and an upper limit of 6.0 mol % or less or 5.5 mol % or less. Any combination of these upper and lower limits may be used. Therefore, the stabilizing element content of the stabilizing element-containing zirconia contained in the first layer (corresponding to the first region) (11) and the second layer (corresponding to the second region) (12) of the present embodiment may be 1.5 mol % or more and 6.0 mol % or less, or 2.5 mol % or more and 5.5 mol % or less. In the sintered body of FIG.
  • the content of the stabilizing element in the stabilizing element-containing zirconia contained in the third layer (corresponding to the third region) (13) is, for example, a lower limit of 2.5 mol% or more. Or 3.0 mol% or more is preferable, and the upper limit is preferably 7.0 mol% or less or 6.0 mol% or less. Any combination of these upper and lower limits may be used. Therefore, the stabilizing element content of the stabilizing element-containing zirconia contained in the third layer (corresponding to the third region) (13) of the present embodiment is 2.5 mol% or more and 7.0 mol% or less, or 3.0 mol % or more and 6.0 mol % or less is sufficient. In FIG.
  • the difference in stabilizing element content between adjacent layers is 0.01 mol% or more, further 0.2 mol% or more, further 0.3 mol% or more, or further 0.5 mol% or more, Furthermore, it is preferably 0.7 mol % or more, further 1.0 mol % or more, and furthermore 1.2 mol % or more.
  • the difference in stabilizing element content increases, the difference in translucency between zirconia layers tends to increase, but warpage may increase. If the difference in content of the stabilizing element in adjacent layers is less than 2.5 mol%, further 2.0 mol% or less, or further 1.7 mol% or less, the translucency of the sintered body naturally changes. Translucency change is likely to be the same as that of teeth.
  • the difference in stabilizing element content between adjacent layers is 0.01 mol % or more and less than 2.5 mol %, 0.2 mol % or more and 2.0 mol % or less, 0.3 mol % or more and 1.7 mol % or less, or Examples include 0.5 mol % or more and 1.7 mol % or less, or 1.2 mol % or more and 1.7 mol % or less.
  • the lower limit is preferably 1.5 mol % or more or 2.5 mol % or more
  • the upper limit is preferably 7.0 mol % or less or 6.0 mol % or less. Any combination of these upper and lower limits may be used. Therefore, the stabilizing element content of the stabilizing element-containing zirconia contained in the first layer (corresponding to the first region) (21) and the second layer (corresponding to the second region) (22) of the present embodiment is preferably 1.5 mol % or more and 7.0 mol % or less, or 2.5 mol % or more and 6.0 mol % or less.
  • the lower limit is preferably 2.0 mol % or more or 2.5 mol % or more
  • the upper limit is preferably 6.0 mol % or less or 5.5 mol % or less. Any combination of these upper and lower limits may be used.
  • the stabilizing element content of the stabilizing element-containing zirconia contained in the third layer (corresponding to the third region) (23) and the fourth layer (corresponding to the third region) (24) of the present embodiment is preferably 2.0 mol % or more and 6.0 mol % or less, or 2.5 mol % or more and 5.5 mol % or less.
  • the difference in stabilizing element content between adjacent layers is 0.01 mol% or more, further 0.2 mol% or more, further 0.3 mol% or more, or further 0.5 mol% or more, Furthermore, it is preferably 0.7 mol % or more, further 1.0 mol % or more, and furthermore 1.2 mol % or more.
  • the difference in content of the stabilizing element in adjacent layers is 2.5 mol% or less, less than 2.5 mol%, further 2.0 mol% or less, or even 1.7 mol% or less, the sintered body Translucency change is likely to be equivalent to that of natural teeth.
  • the difference in content of the stabilizing element between adjacent layers is 0.01 mol % or more and 2.5 mol % or less, 0.01 mol % or more and less than 2.5 mol %, 0.2 mol % or more and 2.0 mol % or less, or 0.3 mol %. % or more and 1.7 mol % or less, further 0.5 mol % or more and 1.7 mol % or less, or 1.2 mol % or more and 1.7 mol % or less.
  • the stabilizing element content of the sintered body is obtained from the following formula, and varies depending on the thickness of each zirconia layer.
  • Content of stabilizing element in sintered body (thickness of first layer/height of sintered body) x content of stabilizing element in first layer + (thickness of second layer/height of sintered body ) x stabilizing element content of the second layer + + (thickness of n-th layer/height of sintered body) x content of stabilizing element in n-th layer
  • the content of the stabilizing element is is the molar proportion of the stabilizing element to the total.
  • the content of each stabilizing element may be obtained by converting the above oxides.
  • the coloring element in this embodiment is an element having a function of coloring zirconia.
  • Specific coloring elements include at least one of transition metal elements and lanthanoid rare earth elements, preferably iron (Fe), cobalt (Co), nickel (Ni), manganese (Mn), and titanium (Ti).
  • Pr praseodymium
  • Nd neodymium
  • Eu europium
  • Gd gadolinium
  • Tb terbium
  • Er erbium
  • Yb ytterbium
  • iron more preferably iron
  • cobalt manganese
  • the coloring elements contained in the sintered body of the present embodiment include coloring elements contained in the state of oxides (hereinafter also referred to as "oxide coloring elements"), and coloring stabilizing elements, etc., which are dissolved in zirconia. At least one of the coloring elements included in the state may be used.
  • Preferred oxide coloring elements include one or more selected from the group of iron, cobalt, nickel, manganese and titanium, and more preferably one or more selected from the group of iron, cobalt and titanium.
  • the sintered body of the present embodiment may contain two or more coloring elements, for example, two to five coloring elements, or three to four coloring elements.
  • the sintered body of the present embodiment preferably contains at least a coloring stabilizing element, more preferably at least one of terbium and erbium, and even more preferably at least terbium and erbium.
  • the type and content of the coloring element contained in each zirconia layer may be appropriately selected in consideration of the shrinkage rate of each layer.
  • the content of the coloring element in the sintered body of the present embodiment has a lower limit of more than 0% by mass, preferably 0, as a mass ratio of the coloring element converted to oxide with respect to the mass of the sintered body of the present embodiment.
  • the content of the coloring element in the sintered body of the present embodiment is, for example, more than 0% by mass and 2.0 mass as a mass ratio of the coloring element converted to oxide with respect to the mass of the sintered body of the present embodiment. % or less, 0.01 mass % or more and 1.2 mass % or less, 0.03 mass % or more and 0.8 mass % or less, or 0.04 mass % or more and 0.3 mass % or less.
  • the content of coloring element is obtained from (Co 3 O 4 +Er 2 O 3 )/(ZrO 2 +Y 2 O 3 +Er 2 O 3 +Co 3 O 4 +Al 2 O 3 ) ⁇ 100.
  • the oxide equivalents of the coloring elements are Pr6O11 for praseodymium , Nd2O3 for neodymium, Tb4O7 for terbium, Er2O3 for erbium, Yb2O3 for ytterbium , Fe2O3 for iron , Cobalt may be Co 3 O 4 , nickel NiO, manganese Mn 3 O 4 and titanium TiO 2 .
  • the content of the coloring element in the sintered body layer of the present embodiment is a mass ratio of the coloring element converted to oxide with respect to the mass of the sintered body of the present embodiment, for example, the lower limit exceeds 0% by mass, It is preferably 0.01% by mass or more, 0.03% by mass or more, or 0.04% by mass or more, and the upper limit is 2.0% by mass or less, 1.2% by mass or less, and 0.8% by mass. or less or 0.3% by mass or less. Any combination of these upper and lower limits may be used.
  • the mass ratio of the coloring element in terms of oxide with respect to the mass of the sintered body of the present embodiment is more than 0% by mass and 2.0% by mass or less, 0.01% by mass or more and 1.2% by mass or less, 0 0.03% by mass or more and 0.8% by mass or less, or 0.04% by mass or more and 0.3% by mass or less.
  • the content of the coloring element for example, the lower limit is 0.01% by mass or more, 0.05% by mass or more, or 0.1% by mass or more, and the upper limit is 2.0% by mass or less or 1.2 mass % or less is mentioned. Any combination of these upper and lower limits may be used.
  • the content of the coloring element in the coloring element-containing zirconia contained in the first layer (corresponding to the first region) (11) and the second layer (corresponding to the second region) (12) of the present embodiment is 0.01% by mass or more and 2.0% by mass or less, or 0.05% by mass or more and 1.2% by mass or less.
  • the content of the coloring element in the coloring element-containing zirconia contained in the third layer (corresponding to the third region) (13) in the sintered body of FIG. .1% by mass or more is preferable, and the upper limit is more preferably 2.0% by mass or less or 1.2% by mass or less. Any combination of these upper and lower limits may be used.
  • the content of the coloring element in the coloring element-containing zirconia contained in the third layer (corresponding to the third region) (13) of the present embodiment is 0.001% by mass or more and 2.0% by mass or less, or It may be 0.1% by mass or more and 1.2% by mass or less.
  • the difference in content of coloring elements in adjacent layers is 0.002% by mass or more, 0.005% by mass or more, 0.01% by mass or more, 0.015% by mass or more, or 0.02% by mass. It is preferable that it is above.
  • the difference in content of the coloring element increases, the difference in color tone between the zirconia layers tends to increase, but warping may also increase.
  • the difference in the content of the coloring element between adjacent layers is 1% by mass or less, further 0.8% by mass or less, or further 0.5% by mass or less, the color tone of the sintered body does not change from that of natural teeth. It is easy to become the same color tone change.
  • the difference in content of the coloring element between adjacent layers is 0.002% by mass or more and 1% by mass or less, 0.005% by mass or more and 0.8% by mass or less, 0.01% by mass or more and 0.5% by mass or less, It is preferably 0.015% by mass or more and 0.5% by mass or less, or 0.02% by mass or more and 0.5% by mass or less.
  • the lower limit is preferably 0.01% by mass or more, 0.05% by mass or more, or 0.1% by mass or more, and the upper limit is 2.0% by mass or less or 1.0% by mass or more. 2 mass % or less is preferable. Any combination of these upper and lower limits may be used.
  • the content of the coloring element in the coloring element-containing zirconia contained in the first layer (corresponding to the first region) (21) and the second layer (corresponding to the second region) (22) of the present embodiment is It may be 0.01% by mass or more and 2.0% by mass or less, or 0.05% by mass or more and 1.2% by mass or less.
  • the lower limit is preferably 0.001% by mass or more or 0.1% by mass or more, and the upper limit is preferably 2.0% by mass or less or 1.2% by mass or less.
  • the coloring element content of the coloring element-containing zirconia contained in the third layer (corresponding to the third region) (23) and the fourth layer (corresponding to the third region) (24) of the present embodiment is It may be 0.001% by mass or more and 2.0% by mass or less, or 0.1% by mass or more and 1.2% by mass or less.
  • the difference in content of the coloring element between adjacent layers is 0.001% by mass or more, 0.002% by mass or more, 0.005% by mass or more, 0.01% by mass or more, and 0.05% by mass. or more or 0.1% by mass or more.
  • the difference in color tone between the zirconia layers tends to increase, but warping may also increase. If the difference in the content of the coloring element between adjacent layers is 1% by mass or less, further 0.8% by mass or less, or further 0.5% by mass or less, the color tone of the sintered body does not change from that of natural teeth. It is easy to become the same color tone change.
  • the difference in content of the coloring element between adjacent layers is 0.002% by mass or more and 1% by mass or less, 0.005% by mass or more and 0.8% by mass or less, 0.01% by mass or more and 0.5% by mass or less, It is preferably 0.015% by mass or more and 0.5% by mass or less, or 0.02% by mass or more and 0.5% by mass or less.
  • the sintered body of the present embodiment may contain alumina, and at least one zirconia layer preferably contains alumina.
  • the alumina content of the sintered body of the present embodiment may be 0% by mass or more, 0% by mass or more and 0.15% by mass or less, and further 0% by mass as the ratio of the mass of alumina to the mass of the sintered body. % or more and 0.10 mass % or less, or further 0 mass % or more and 0.07 mass % or less.
  • the lower limit of the alumina content exceeds 0% by mass, preferably 0.005% by mass or more or 0.01% by mass or more, and the upper limit of the alumina content is 0.005% by mass or more or 0.01% by mass or more. 15% by mass or less, 0.10% by mass or less, or 0.07% by mass or less. Any combination of these upper and lower limits may be used. Therefore, the alumina content is, for example, more than 0% by mass and 0.15% by mass or less, 0.005% by mass or more and 0.10% by mass or less, or 0.01% by mass or more and 0.07% by mass or less Things are mentioned.
  • each zirconia layer is also within the same range as described above.
  • the alumina content of each zirconia layer can affect the thermal shrinkage behavior during the calcination stage.
  • the alumina content of each zirconia layer is arbitrary, and although each zirconia layer may have a different alumina content, it is preferred that they have the same alumina content.
  • the lower limit of the difference in alumina content between adjacent zirconia layers is more than 0% by mass, and is 0.005% by mass or more.
  • the upper limit of the difference in alumina content is 0.15% by mass or less, 0.1% by mass or less, 0.03% by mass or less, or 0.01% by mass or less. Any combination of these upper and lower limits may be used. Therefore, the difference in alumina content between adjacent zirconia layers is more than 0% by weight and 0.15% by weight or less, more than 0% by weight and 0.1% by weight or less, more than 0% by weight and 0.03% by weight or less, Alternatively, it can be exemplified that it is 0.005% by mass or more and 0.01% by mass or less.
  • the non-colored stabilizing element is yttrium (Y 2 O 3 ), and the colored stabilizing element is erbium (Er 2 O 3 ), alumina
  • the content can be determined as ⁇ Al 2 O 3 /(ZrO 2 +Y 2 O 3 +Er 2 O 3 +Al 2 O 3 ) ⁇ 100 (% by mass).
  • the sintered body of the present embodiment does not substantially contain silica (SiO 2 ), and more preferably the amount of silica is below the measurable limit.
  • the sintered body of the present embodiment preferably includes at least a zirconia layer containing zirconia whose crystal phase is at least one of tetragonal (T phase) and cubic (C phase). It is more preferable to include a zirconia layer containing zirconia as a phase, more preferably a zirconia layer containing zirconia having a tetragonal crystal as a main phase and a zirconia layer containing zirconia having a cubic crystal as a main phase.
  • the “main phase” in the present embodiment means a crystal phase having the largest existence ratio (percentage of peak integrated intensity) among the crystal phases of zirconia. The abundance ratio can be obtained from the XRD pattern of the surface of the sintered body.
  • the following conditions can be exemplified as the conditions for measuring the XRD pattern of the surface of the sintered body.
  • the obtained XRD pattern is subjected to smoothing treatment and background removal treatment, and profile fitting is performed with a split pseudo-Voigt function to obtain the ratio of tetragonal and cubic crystals (the ratio of peak integrated intensity), and a crystal phase with a high ratio should be the main phase.
  • XRD pattern measurement and fitting are performed using a general-purpose powder X-ray diffractometer (e.g., Ultima IV, manufactured by RIGAKU) and an analysis program attached to the X-ray diffractometer (e.g., integrated powder X-ray analysis software PDXL Ver.2.2 , manufactured by RIGAKU).
  • a general-purpose powder X-ray diffractometer e.g., Ultima IV, manufactured by RIGAKU
  • an analysis program attached to the X-ray diffractometer e.g., integrated powder X-ray analysis software PDXL Ver.2.2 , manufactured by RIGAKU.
  • each sintered body layer constituting the sintered body>
  • the thicknesses of the first layer, the third layer and the second layer are approximately the same.
  • the thickness of each layer hereinafter also referred to as "layer thickness" may be different, and the layer thickness of any one of the first to third layers may be different.
  • the layer thicknesses of the first to third layers may For example, as the layer thicknesses of the first to third layers, the lower limit of the layer thickness is 1 mm or more, further 2 mm or more, or further 3 mm or more, and the upper limit of the layer thickness is 20 mm or less, and further 15 mm or less, or even 10 mm or less. Any combination of these upper and lower limits may be used. Therefore, the layer thicknesses of the first to third layers are, for example, 1 mm or more and 20 mm or less, further 2 mm or more and 15 mm or less, or further 3 mm or more and 10 mm or less. More specifically, in the sintered body of FIG.
  • the layer thickness of the first layer is preferably 0.5 mm or more and 10 mm or less
  • the layer thickness of the second layer is preferably 0.5 mm or more and 10 mm or less.
  • the thickness of the layer is preferably 1 mm or more and 20 mm or less.
  • the layer thickness of the first layer is preferably 0.5 mm or more and 10 mm or less
  • the layer thickness of the second layer is preferably 0.5 mm or more and 10 mm or less.
  • the layer thickness of each layer in the intermediate layer is preferably 1 mm or more and 10 mm or less.
  • the shape of the sintered body of the present embodiment may be any shape according to the purpose, and at least one selected from the group of spherical, elliptical, disk-like, cylindrical, cubic, rectangular parallelepiped and polyhedral shapes. , a shape suitable for dental materials such as dental prosthetic materials such as crowns, bridges, onlays and onlays, and any other shape according to the intended use.
  • the spherical shape may include shapes similar to true spheres other than true spheres, such as a substantially spherical shape
  • the polyhedral shape may include shapes similar to polyhedrons, such as substantially polyhedral shapes, in addition to polyhedrons.
  • the dimensions of the sintered body of the present embodiment are arbitrary, and can be exemplified by a length of 10 mm or more and 120 mm or less, a width of 12 mm or more and 120 mm or less, and a height of 6 mm or more and 40 mm or less.
  • the thickness of the sintered body of the present embodiment in the stacking direction ie, the height of the sintered body, is arbitrary, but may be, for example, 4 mm or more and 40 mm or less, more preferably 5 mm or more and 30 mm or less.
  • the sintered body of the present embodiment has a warpage (hereinafter simply referred to as "warp") measured using a thickness gauge (hereinafter also simply referred to as "gauge”) conforming to JIS B 7524: 2008. 0 mm or less.
  • warp a warpage measured using a thickness gauge
  • gauge a thickness gauge conforming to JIS B 7524: 2008. 0 mm or less.
  • a sintered body having a structure including three or more zirconia layers is warped in the stacking direction (or the direction opposite to the stacking direction) by sintering. When such a sintered body is arranged on a horizontal plate, a gap is formed between the sintered body and the horizontal plate.
  • the warp in this embodiment is a value measured using a gauge.
  • the warpage of the sintered body of the present embodiment is preferably 0.3 mm or less, 0.2 mm or less, 0.1 mm or less, or 0.05 mm or less.
  • the sintered body preferably has no warpage (warpage of 0 mm), but the sintered body of the present embodiment may have warpage that cannot be measured with a gauge (warpage of 0 mm or more).
  • the warp of the sintered body of this embodiment exceeds 0 mm, and can be exemplified by 0.01 mm or more.
  • the warpage is 0.06 mm or less, more preferably 0.05 mm or less, or even less than the measurable limit (less than 0.03 mm).
  • the warp can be measured by the maximum thickness of a gauge that can be inserted into a gap formed when the sintered body is arranged so that the convex portion is in contact with the horizontal plate.
  • the warp of the sintered body of the present embodiment is 0 mm or more and 0.3 mm or less, 0 mm or more and 0.05 mm or less, 0 mm or more and less than 0.03 mm, or more than 0 mm and less than 0.03 mm.
  • FIG. 5 is a schematic diagram showing a method of measuring warpage.
  • a sintered body (500) shows a cross section of a disk-shaped sample, and shows a sintered body that is warped in the stacking direction (Y-axis direction).
  • the warp of the sintered body (500) is emphasized for explanation.
  • the sintered compact (500) having the uneven shape is arranged so that the convex portion is in contact with the horizontal plate (51).
  • a gap is formed between the surface where the sintered body (500) and the horizontal plate (51) are in contact (hereinafter also referred to as "bottom surface") and the horizontal plate (51).
  • gauge (52A) is located below the bottom surface of the sintered body (500) and shows a state in which it has been inserted into the gap, while the gauge (52B) is the sintered body (500). It is not positioned at the bottom of the bottom surface and cannot be inserted into the gap.
  • Gauges (52A) and (52B) in FIG. 5 are gauges that differ in thickness by one step (for example, 0.01 mm), and the warp of the sintered body (500) is the thickness of the gauge (52A). In order to simplify the explanation, FIG.
  • FIG 5 shows both the gauges (52A) and (52B) inserted, but the warp measurement is performed by inserting the gauges into the gaps in order from the thinner gauges. (eg, after measuring using gauge (52A), remove it and then measure using thicker gauge (52B), etc.).
  • the warpage (hereinafter also referred to as "deformation amount") with respect to the dimensions of the sintered body is 1.0 or less, 0.5 or less, 0.2 or less, or 0.15 or less. is preferred.
  • the deformation amount is 0 or more, further 0.01 or more, or further 0.05 or more.
  • the amount of deformation may be 0 or more and 1.0 or less, 0 or more and 0.15 or less, 0.01 or more and 1.0 or less, or 0.05 or more and 0.15 or less.
  • the amount of deformation can be obtained from the following formula (2).
  • the dimension of the sintered body is the size of the sintered body in the direction perpendicular to the direction of warpage. Since the sintered body (500) in FIG. 5 is along the stacking direction (Y-axis direction), the dimension of the sintered body (500) is the horizontal direction (X-axis direction) perpendicular to the stacking direction. is the magnitude of (53).
  • the dimensions can be measured by known measuring methods using vernier calipers, micrometers, or the like. For example, in the case of a disk-shaped or columnar laminate, the dimension of the sintered body indicates the diameter of the sintered body.
  • the dimensions of the sintered body can be measured using a vernier caliper.
  • the diameter of the upper end and the diameter of the lower end are measured at four points each, the average value of the diameters of the upper end and the lower end is obtained, and the average value of the obtained values is used as the dimension of the laminate.
  • the sintered body of the present embodiment has a lower limit of density measured by a method according to JIS R 1634 of 5.7 g/cm 3 or more or 5.9 g/cm 3 or more, and an upper limit of density of For example, it is 6.3 g/cm 3 or less or 6.1 g/cm 3 or less. Any combination of these upper and lower limits may be used. Therefore, the density of the sintered body of the present embodiment is, for example, 5.7 g/cm 3 or more and 6.3 g/cm 3 or less, preferably 5.9 g/cm 3 or more and 6.1 g/cm 3 or less.
  • a density within this range corresponds to a relative density of 99% or more, and is a density that provides a so-called dense sintered body with practical strength.
  • the color tone of the sintered body of the present embodiment or each zirconia layer can be evaluated, for example, by color tone according to the L * a * b * color system.
  • the color tone of the sintered body or each zirconia layer (each sintered body layer) of the present embodiment has a lower limit value of lightness L * indicated by the L * a * b * color system of 50 or more or 55 or more,
  • the upper limit of lightness L * is 80 or less or 70 or less
  • the lower limit of hue a * is -5 or more or -3 or more
  • the upper limit of hue a * is 15 or less or 10 or less
  • the lower limit of b * is 0 or more or 3 or more
  • the upper limit of hue b * is 45 or less or 35 or less. Any combination of these upper and lower limits may be used.
  • the color tone of the sintered body or each zirconia layer (each sintered body layer) of the present embodiment is such that the lightness L * indicated by the L * a * b * color system is 50 or more and 80 or less, or 55 or more. 70 or less, the hue a * is -5 or more and 15 or less, or -3 or more and 10 or less, and the hue b * is 0 or more and 45 or less, or 3 or more and 35 or less.
  • the sintered body exhibits a color tone similar to that of natural teeth.
  • the lower limit of the absolute value ( ⁇ C * ) of the difference in saturation C * between adjacent layers is 0.1 or more, 0.3 or more, 1.0 or more, or 1.5 or more, and the absolute value ( ⁇ C * ) is 20.0 or less, 15.0 or less, 10.0 or less, or 5.0 or less.
  • the absolute value ( ⁇ C * ) of the difference in chroma C * between adjacent layers is, for example, 0.1 or more and 20.0 or less, or 0.3 or more and 15.0 or less. , 1.0 to 10.0, or 1.5 to 5.0.
  • the layered product can be visually recognized as having a vivid gradation close to that of natural teeth.
  • the lower limit of the absolute value ( ⁇ L * ) of the difference in lightness L * between adjacent layers is 1.0 or more, further 1.5 or more
  • the upper limit of the absolute value ( ⁇ L * ) is 30. .0 or less, and further 15.0 or less.
  • the absolute value ( ⁇ L * ) of the difference in lightness L * between adjacent layers is 1.0 or more and 30.0 or less, further 1.5 or more and 15.0 or less.
  • Color tone (L * , a * and b * ) and C * were measured using a colorimetric color difference meter (e.g., ZE6000, manufactured by Nippon Denshoku Industries Co., Ltd.) equipped with an illumination/light-receiving optical system conforming to JIS Z 8722 geometric condition c. can be used and asked for.
  • the following conditions can be exemplified in a method of placing a zero calibration box on a measurement sample (so-called black background measurement).
  • the color tone of the sintered body of this embodiment can be measured by cutting out an arbitrary portion of the sintered body in the horizontal direction and processing the sample so that the sample thickness is 2.8 ⁇ 0.1 mm.
  • Light source D65 light source Viewing angle: 2° Measurement method: SCI
  • the sintered body of the present embodiment preferably includes at least a translucent zirconia layer. Furthermore, at least the lower limit of the total light transmittance (hereinafter also simply referred to as "total light transmittance") for CIE standard light source D65 at a sample thickness of 1.0 ⁇ 0.1 mm is 15% or more, 20% or more, 30 %, 32% or more, or 35% or more, and the upper limit of the total light transmittance is 50% or less, 45% or less, or 42% or less. Any combination of these upper and lower limits may be used.
  • the sintered body of the present embodiment has a zirconia layer having a total light transmittance of, for example, 15% or more and 50% or less, further 20% or more and 45% or less, further 32% or more and 42% or less. is preferred.
  • the sintered body of this embodiment absorbs different wavelengths of light depending on its coloration. Therefore, the total light transmittance for light containing different wavelengths, such as CIE standard light source D65, is suitable as an indicator of translucency.
  • the lower limit of the difference in total light transmittance between adjacently laminated zirconia layers is preferably 1% or more or 1.5% or more.
  • the upper limit is preferably 10% or less or 5% or less. Any combination of these upper and lower limits may be used. Therefore, in the sintered body of the present embodiment, the difference in total light transmittance between adjacently laminated zirconia layers is, for example, 1% or more and 10% or less, or 1.5% or more and 5% or less. preferable.
  • the total light transmittance is measured by a method according to JIS K 7361, CIE standard light source D65 is used as incident light, and it can be obtained as a transmittance value that is the sum of the diffuse transmittance and the linear transmittance for the incident light.
  • Cut out an arbitrary part of the sintered body in the horizontal direction use this as a sample with a thickness of 1.0 ⁇ 0.1 mm and a surface roughness (Ra) ⁇ 0.02 ⁇ m, and use a general turbidity meter (haze meter ;For example, NDH4000, manufactured by Nippon Denshoku Industries) is used to irradiate the sample with light from the CIE standard light source D65, and the transmittance of the sample is measured by collecting the transmitted light with an integrating sphere (diffuse transmittance and linear transmittance transmittance) is measured and may be taken as the total light transmittance.
  • haze meter haze meter
  • NDH4000 manufactured by Nippon Denshoku Industries
  • the three-point bending strength of each zirconia layer (each sintered body layer) in the sintered body of the present embodiment is 500 MPa or more, 550 MPa or more, or 600 MPa or more measured by a method according to JIS R 1601. more preferred.
  • Three-point bending strength can be exemplified by less than 1200 MPa, and further less than 1160 MPa.
  • Preferred three-point bending strength is 500 MPa sulfur less than 1200 MPa, 550 MPa to 1160 MPa, or 600 MPa to 1160 MPa.
  • FIG. 6 is a schematic diagram showing how the three-point bending strength of the zirconia layer (sintered body layer) (600) is measured.
  • a measurement sample used for measuring the three-point bending strength is a rectangular parallelepiped sintered body produced with the thickness in the stacking direction and the width and length in the horizontal direction. As shown in FIG. 6, the three-point bending strength can be measured by applying a load (61) perpendicular to the length of the measurement sample (600). The measurement sample should be arranged so that the load (61) is applied in the middle of the inter-fulcrum distance (62).
  • Three-point bending strength was measured using a pillar-shaped sintered body with a fulcrum distance of 30 mm, a width of 4 mm, and a thickness of 3 mm as a measurement sample, and the crosshead speed was 0.5 mm / min.
  • the average value of 10 measurements. is the three-point bending strength of the zirconia layer (sintered body layer) according to the present embodiment.
  • the calcined body according to this embodiment is A calcined body of a zirconia composition,
  • the zirconia composition contains (iii) a stabilizing element-containing zirconia composition having a necking structure, or (iv) a zirconia composition containing a stabilizing element-containing zirconia having a necking structure and a coloring element. do.
  • the calcined body has three or more regions laminated in layers, and the content of at least one of the stabilizing element and the coloring element is different in two adjacent regions among the regions.
  • the content of the stabilizing element contained in the first region located at one end and the content of the stabilizing element contained in the second region located at the other end is 2.0 mol % or less.
  • the calcined body of another form according to the present embodiment is A calcined body of a zirconia composition,
  • the zirconia composition contains (iii) a stabilizing element-containing zirconia composition having a necking structure, or (iv) a zirconia composition containing a stabilizing element-containing zirconia having a necking structure and a coloring element. do.
  • the calcined body has three or more regions laminated in layers, and the content of at least one of the stabilizing element and the coloring element is different in two adjacent regions among the regions. and Among the laminated regions, the difference (shrinkage rate difference) is 0.4% or less.
  • a calcined body is a layered body composed of a structure having a necking structure, ie, so-called calcined particles.
  • a calcined body can be processed as necessary and used as a precursor of a sintered body, and is also called a pre-sintered body, a soft sintered body, or a semi-sintered body.
  • the necking structure is a structure possessed by zirconia heat-treated below the sintering temperature, and is a structure in which zirconia particles are chemically adhered to each other. As shown in FIG. 7, the zirconia (71) contained in the zirconia composition layer of the calcined body can be partially confirmed as the particle shape of zirconia in the powder composition.
  • the structure having the necking structure is a structure made of zirconia in the initial stage of sintering. This is different from the sintered structure, ie the structure consisting of zirconia crystal grains in the later stages of sintering. Therefore, the calcined body of the present embodiment is a zirconia composition layer composed of zirconia particles having a necking structure of zirconia containing a stabilizing element, or, when a coloring element is contained, a necking structure of zirconia containing a stabilizing element. It can also be regarded as a laminate having three or more zirconia composed of zirconia particles having a structure and zirconia composition layers containing a coloring element.
  • the calcined body is a zirconia composition layer made of zirconia containing a stabilizing element having a necking structure, or when a coloring element is contained, zirconia containing a stabilizing element having a necking structure and a coloring element.
  • these zirconia composition layers are collectively referred to simply as "zirconia composition layer” or “composition layer”). It has a structure equivalent to the laminated structure shown in FIG. 1 or FIG.
  • the stabilizing element and the coloring element may be in the form of a solid solution in zirconia, or in the form of oxides or precursors thereof.
  • the zirconia composition layer is also referred to as a calcined body layer.
  • Preferred embodiments of the calcined body of the present disclosure include a calcined body described in the following mode (C) and a calcined body described in the following mode (D).
  • the calcined body of the present embodiment is less warped and less deformed.
  • such a calcined body can effectively form a sintered body with reduced warpage and less deformation while having translucency and color gradation similar to those of natural teeth when viewed visually.
  • the relationship between the first region (eg, the first layer (11)) located at one end and the second region (eg, the second layer (12)) located at the other end can be adjusting the shrinkage ratio of the regions (layers) located at both ends, the warping of the calcined body can be effectively suppressed. Therefore, a zirconia composition layer having an arbitrary composition can be laminated for each intermediate layer disposed between the first layer (11) and the second layer (12).
  • the difference between the content of the stabilizing element contained in the first region and the content of the stabilizing element contained in the second region is 2.0 mol% or less, 1.8 mol % or less is preferable, 1.5 mol % or less is more preferable, and 0.8 mol % or less is even more preferable.
  • the difference between the content of the stabilizing element contained in the first region and the content of the stabilizing element contained in the second region is preferably small. .1 mol % or more, or 0.3 mol % or more.
  • the difference between the content of the stabilizing element contained in the first region and the content of the stabilizing element contained in the second region is 0 mol% or more and 2.0 mol% or less, and more than 0 mol% and 1.8 mol% or less. , 0.1 mol % to 1.5 mol %, or 0.3 mol % to 0.8 mol %.
  • the contraction rate of the calcined body in the first region located at one end of the laminated regions and the calcined body in the second region located at the other end is 0.4% or less.
  • the shrinkage ratio of the calcined body is set to a close value (specifically, 0.4% or less).
  • a close value specifically, 0.4% or less.
  • first region e.g., the first layer (11)
  • second region e.g., the second layer (12)
  • warping of the calcined body can be effectively suppressed by adjusting the shrinkage ratio of the regions (layers) located at both ends. Therefore, a zirconia composition layer having an arbitrary composition can be laminated for each layer of the intermediate layer disposed between the first layer (11) and the second layer (12).
  • the difference between the shrinkage rate of the calcined body in the first region and the shrinkage rate of the calcined body in the second region is 0.4% or less, 0.36% or less, 0.3% or less or 0.2% or less is preferable.
  • the difference between the shrinkage rate of the calcined body in the first region and the shrinkage rate of the calcined body in the second region is preferably small, for example, 0% or more, 0% or more, 0.01% or more. Alternatively, it may be 0.02% or more.
  • the difference between the shrinkage rate of the calcined body in the first region and the shrinkage rate of the calcined body in the second region is 0% or more and 0.4% or less, more than 0% and 0.36% or less, 0.01% 0.3% or less, or 0.02% or more and 0.2% or less.
  • the shrinkage ratios of the first region (eg, the first layer (11)) located at one end and the second region (eg, the second layer (12)) located at the other end are as follows.
  • a powder composition which is a sample for shrinkage measurement, was obtained by filling a mold with raw material powder of zirconia having the same composition as the first layer (11) and the second layer (12), followed by uniaxial press molding and CIP treatment. form a layer.
  • the powder composition layer is calcined at 800° C. or more and less than 1200° C. to obtain a zirconia composition layer.
  • the shrinkage ratio of the zirconia composition layer is determined by the method described in the [Evaluation method for shrinkage ratio] described in the section ⁇ Form of (B)>> in the above (sintered body).
  • the method of preparing the sample for shrinkage rate measurement and the calcination conditions are as described above.
  • the zirconia contained in the calcined body is preferably in a state in which zirconia obtained by heat-treating a zirconia sol is heat-treated below the sintering temperature. It is more preferable that the zirconia is heat-treated below the sintering temperature, and more preferably the zirconia obtained by heat-treating the zirconia sol obtained by hydrolysis of zirconium oxychloride is heat-treated below the sintering temperature.
  • the content of the stabilizing element in zirconia containing stabilizing element contained in first composition layer (corresponding to first region), stabilizing element contained in second composition layer (corresponding to second region) are The content of the stabilizing element may be the same as that of the first layer, the second layer, and the third layer (intermediate layer) described above.
  • the content of the stabilizing element in each composition layer in the calcined body is arbitrary, but may be the same as in the sintered body layer of the present embodiment described above. More preferably, the calcined body contains at least a zirconia composition layer containing zirconia having a tetragonal or cubic crystal as a main phase.
  • the calcined body preferably has a warp of 1.0 mm or less, 0.5 mm or less, 0.3 mm or less, 0.2 mm or less, 0.1 mm or less, or 0.05 mm or less.
  • the calcined body preferably has no warpage (warpage of 0 mm), but may have warpage that cannot be measured with a gauge (warpage of 0 mm or more). It can be exemplified that the calcined body has a warpage of more than 0 mm, more preferably 0.01 mm or more.
  • the warp is 0.06 mm or less, more preferably 0.05 mm or less, or even less than the measurable limit (less than 0.03 mm).
  • Warp of the calcined body is 0 mm or more and 0.3 mm or less, 0 mm or more and 0.05 mm or less, 0 mm or more and less than 0.03 mm, or more than 0 mm and less than 0.03 mm.
  • the calcined body preferably has a deformation amount of 1.0 or less, 0.5 or less, 0.2 or less, or 0.15 or less.
  • the deformation amount is 0 or more, further 0.01 or more, or further 0.05 or more.
  • the amount of deformation may be 0 or more and 1.0 or less, 0 or more and 0.15 or less, 0.01 or more and 1.0 or less, or 0.05 or more and 0.15 or less.
  • the calcined body has a lower limit of density of 2.4 g/cm 3 or more or 3.1 g/cm 3 or more, and an upper limit of density of 3.7 g/cm 3 or less or 3.5 g/cm 3 .
  • the following can be exemplified. Any combination of these upper and lower limits may be used. Therefore, the density of the calcined body is 2.4 g/cm 3 or more and 3.7 g/cm 3 or less, preferably 3.1 g/cm 3 or more and 3.5 g/cm 3 or less. This range of densities corresponds to a relative density of 40% to 60%.
  • the calcined body may be a laminate having a strength suitable for processing such as CAD/CAM processing.
  • the density of the calcined body is determined from the mass determined by mass measurement and the volume determined by dimensional measurement.
  • the color tone of the zirconia composition layer contained in the calcined body may be different from that of the sintered body (sintered body layer) obtained by sintering this.
  • the calcined body and each composition layer are opaque and have a total light transmittance of 0%, but when considering measurement errors, the total light transmittance is 0% or more and 0.2%
  • the following can be exemplified.
  • the calcined body and each composition layer only need to have strength to the extent that defects are unlikely to occur during processing such as CAD/CAM and cutting.
  • the Vickers hardness can be measured using a general Vickers tester (for example, Q30A, manufactured by Qness) equipped with a regular square pyramid indenter made of diamond.
  • the indenter is statically pressed into the surface of the measurement sample, and the diagonal length of the indentation mark formed on the surface of the measurement sample is visually measured.
  • Hv is the Vickers hardness (HV)
  • F is the measured load (1 kgf)
  • d is the diagonal length of the indentation mark (mm)
  • ⁇ is the facing angle of the indenter (136°).
  • the Vickers hardness measurement conditions include the following conditions.
  • Measurement sample Disk shape with a thickness of 2.0 ⁇ 0.5 mm
  • Measurement load 1 kgf
  • the sample to be measured may be prepared by cutting out an arbitrary portion of the calcined body in the horizontal direction and polishing the measurement surface with #800 water-resistant abrasive paper to remove irregularities exceeding 0.1 mm.
  • the laminate of the present embodiment can be used for known zirconia applications such as decorative members, structural materials, and optical materials. It can be suitably used as a material, and can be used as a dental material containing the sintered body of the present embodiment.
  • the laminate when the laminate is a calcined body, it can be suitably used as a precursor of dental materials such as dentures such as crowns and bridges, and dental prosthetic materials such as blanks, discs, blocks and mill blanks. It can be provided as a precursor of these.
  • the laminate of the sintered body or calcined body of this embodiment can be used as a dental material. Next, a method for manufacturing each laminate (specifically, a sintered body, a calcined body, and a molded body) of this embodiment will be described below.
  • a method for manufacturing the sintered body of the present embodiment is as follows. Sintering a compact at 1200° C. or higher and 1600° C. or lower, in which three or more layers of a powder composition layer composed of a zirconia raw material powder containing a stabilizing element-containing zirconia and, if a coloring element is contained, a coloring element, are laminated.
  • a method for producing a sintered body, comprising: Another method for producing the sintered body of the present embodiment is as follows.
  • a molded body in which three or more powder composition layers made of zirconia raw material powder containing stabilizing element-containing zirconia and, if a coloring element is contained, a coloring element, is laminated is calcined at 800 ° C. or more and less than 1200 ° C. and sintering the calcined body at 1200° C. or higher and 1600° C. or lower.
  • the method for manufacturing the calcined body of the present embodiment is as follows.
  • a molded body in which three or more layers of a powder composition layer composed of zirconia raw material powder containing stabilizing element-containing zirconia and a coloring element when containing a coloring element are laminated is calcined at 800 ° C. or more and less than 1200 ° C.
  • a method for manufacturing a molded body for manufacturing the sintered body or the calcined body is as follows.
  • a method for producing a molded body comprising a step of laminating three or more powder composition layers composed of zirconia raw material powder containing stabilizing element-containing zirconia and, if a coloring element is contained, a coloring element, to produce a molded body.
  • the powder composition layer is also referred to as a compact layer.
  • the molded body to be subjected to the production method of the present embodiment is a powder composition layer made of raw material powder of zirconia containing a stabilizing element, or when a coloring element is contained, zirconia containing zirconia containing a stabilizing element and a coloring element. Three or more powder composition layers made of raw material powder are laminated.
  • the compact is a laminate obtained by stacking powder composition layers, and the compact can be provided as a precursor of a calcined body or a sintered body.
  • the molded body has a powder composition layer made of a powder composition of zirconia containing a stabilizing element, or when a coloring element is contained, a powder composition containing zirconia containing a stabilizing element and a coloring element.
  • these powder composition layers are hereinafter collectively referred to simply as “powder layers”. It has a structure equivalent to the laminated structure shown in FIG. 1 or FIG. Therefore, the compact can also be regarded as a laminate comprising three or more layers containing zirconia powder containing a stabilizing element.
  • the stabilizing element and the coloring element may be in a solid solution state in zirconia, or may be in a state of an oxide or its precursor.
  • a precursor one or more selected from the group of sulfides, chlorides, nitrates, sulfates, hydroxides and oxyhydroxides, and one selected from the group of chlorides, hydroxides and oxyhydroxides
  • the coloring element preferably contains at least an oxide.
  • the zirconia contained in the powder layer is preferably heat-treated zirconia, more preferably heat-treated zirconia sol obtained by hydrolysis of a zirconium compound, and hydrolysis of zirconium oxychloride. It is further preferred that the zirconia sol that has been heat-treated is heat-treated zirconia.
  • the zirconia contained in the powder layer is preferably zirconia powder.
  • the zirconia powder preferably has a lower limit of average particle size of 0.3 ⁇ m or more or 0.4 ⁇ m or more, and an upper limit of average particle size of 0.7 ⁇ m or less or 0.5 ⁇ m or less. Any combination of these upper and lower limits may be used. Therefore, the average particle size of the zirconia powder is preferably, for example, 0.3 ⁇ m or more and 0.7 ⁇ m or less, or 0.4 ⁇ m or more and 0.5 ⁇ m or less.
  • the zirconia powder preferably has a BET specific surface area of 7.5 m 2 /g or more and 15 m 2 /g or less.
  • BET specific surface area 7.5 m 2 /g or more and 15 m 2 /g or less.
  • the lower limit of the BET specific surface area is 8 m 2 /g or more, 9 m 2 /g or more, or 9.5 m 2 /g or more, and the upper limit of the BET specific surface area is preferably 15 m 2 /g or less, 13 m 2 /g or less, or 11 m 2 /g or less. Any combination of these upper and lower limits may be used.
  • the BET specific surface area of the zirconia powder is, for example, 8 m 2 /g or more and 15 m 2 /g or less, 9 m 2 /g or more and 13 m 2 /g or less, or 9.5 m 2 /g or more and 11 m 2 /g or less. is preferred.
  • the BET specific surface area is a BET specific surface area measured according to JIS R 1626, and may be measured by the BET 5-point method by the carrier gas method using nitrogen as the adsorption gas. The following conditions can be exemplified as specific measurement conditions for the BET specific surface area.
  • Adsorption medium N2
  • Adsorption temperature -196°C
  • Pretreatment conditions degassing treatment in air at 250° C. for 1 hour or more
  • the BET specific surface area can be measured using a general device (for example, Tristar II 3020, manufactured by Shimadzu Corporation).
  • the coloring element contained in the powder layer is preferably in at least one of a state of being mixed with zirconia powder and a state of solid solution in zirconia.
  • the coloring element powder and the zirconia powder may be mixed.
  • the molded body may contain a binder.
  • a binder By including a binder, the shape retention of the molded article is enhanced.
  • a known binder used for molding ceramics can be used, and an organic binder is preferred.
  • the organic binder is one or more selected from the group of polyvinyl alcohol, polyvinyl butyrate, wax and acrylic resin, preferably one or more of polyvinyl alcohol and acrylic resin, more preferably acrylic resin.
  • the acrylic resin is a polymer containing at least one of acrylic acid ester and methacrylic acid ester.
  • acrylic resins include one or more selected from the group consisting of polyacrylic acid, polymethacrylic acid, acrylic acid copolymers and methacrylic acid copolymers, and derivatives thereof.
  • acrylic resin binder one or more selected from the group of acrylic resins used for ceramic powders, AS-1100, AS-1800 and AS-2000 (all product names. Toagosei company) can be exemplified.
  • the content of the stabilizing element in the zirconia containing the stabilizing element contained in the first powder layer, the content of the stabilizing element in the zirconia containing the stabilizing element contained in the second powder layer, and the third powder layer may be the same as the stabilizing element content of the above-described first, second, and third layers (intermediate layers).
  • the content of the stabilizing element and the coloring element in each powder layer in the molded body is arbitrary, but may be the same as in the sintered body of the present embodiment described above.
  • the lower limit of the content of the binder in each powder layer is 1.5% by mass or more, 1.5% by mass or more, 2 0% by mass or more or 2.5% by mass or more, and the upper limit is preferably 8.0% by mass or less, 6.0% by mass or less, or 5.5% by mass or less. Any combination of these upper and lower limits may be used. Therefore, the content of the binder in each powder layer is, for example, 1.5% by mass or more and 8.0% by mass or less, 2.0% by mass or more and 6.0% by mass or less, or 2.5% by mass or more5 It is preferably 0.5% by mass or less.
  • the binder content is the mass ratio of the binder to the mass of the powder composition in the powder layer excluding the binder ( ⁇ binder/(powder composition-binder) ⁇ 100).
  • the binder content is the mass ratio of the binder to the mass of the powder composition in the powder layer excluding the binder ( ⁇ binder/(powder composition-binder) ⁇ 100).
  • the powder composition contained in the powder layer is a zirconia powder, a coloring element if it contains a coloring element, and a powder in which a binder is granulated if it contains a binder ( hereinafter also referred to as “granulated powder"), and more preferably granulated powder granulated by spray drying or the like (hereinafter also referred to as "powder granules").
  • the particle size of the granulated powder is arbitrary, but the average aggregate size (hereinafter also referred to as "average particle size") can be exemplified by a lower limit of 1 ⁇ m or more or 5 ⁇ m or more, and an upper limit of 150 ⁇ m or less and 100 ⁇ m or less. , 50 ⁇ m or less, or 30 ⁇ m or less. Any combination of these upper and lower limits may be used. Therefore, the particle size of the granulated powder can be exemplified by an average aggregate size of 1 ⁇ m to 150 ⁇ m, 1 ⁇ m to 100 ⁇ m, 5 ⁇ m to 50 ⁇ m, or 5 ⁇ m to 30 ⁇ m.
  • the average aggregate diameter is the diameter corresponding to cumulative 50% in volume particle size distribution measurement.
  • the volume particle size distribution is a value that can be measured by a general-purpose device (eg, MT3100II, manufactured by Microtrack Bell), and is the volume diameter of particles that approximate a spherical shape.
  • MT3100II manufactured by Microtrack Bell
  • the granulated powder is sieved through a sieve with an opening of 125 ⁇ m, and the granulated powder that has passed through the sieve is measured.
  • the compact preferably contains at least a powder layer containing zirconia having a tetragonal or cubic crystal as a main phase.
  • the molded article preferably has a warp of 1.0 mm or less, 0.3 mm or less, 0.2 mm or less, 0.1 mm or less, or 0.05 mm or less.
  • the molded body preferably has no warpage (warpage of 0 mm), but may have warpage that cannot be measured with a gauge (warpage of 0 mm or more).
  • the molded article has a warpage of more than 0 mm, and more preferably 0.01 mm or more.
  • the warpage is 0.06 mm or less, more preferably 0.05 mm or less, or even less than the measurable limit (less than 0.03 mm).
  • the warp of the compact is 0 mm or more and 0.06 mm or less, 0 mm or more and 0.05 mm or less, 0 mm or more and less than 0.03 mm, or more than 0 mm and less than 0.03 mm.
  • the compact preferably has a deformation amount of 1.0 or less, 0.5 or less, 0.2 or less, or 0.15 or less.
  • the deformation amount is 0 or more, further 0.01 or more, or further 0.05 or more.
  • the amount of deformation may be 0 or more and 1.0 or less, 0 or more and 0.15 or less, 0.01 or more and 1.0 or less, or 0.05 or more and 0.2 or less.
  • the molded body can be exemplified by having a lower limit of density of 2.4 g/cm 3 or more or 3.1 g/cm 3 or more, and an upper limit of density of 3.7 g/cm 3 or less or 3.5 g/cm 3 .
  • the following can be exemplified. Any combination of these upper and lower limits may be used. Therefore, the density of the compact can be exemplified to be 2.4 g/cm 3 or more and 3.7 g/cm 3 or less, or 3.1 g/cm 3 or more and 3.5 g/cm 3 or less. This range of densities corresponds to a relative density of 40% to 60%. In some cases, the density of the molded body is approximately the same as the density of the calcined body.
  • the density of the compact is determined from the mass determined by mass measurement and the volume determined by dimensional measurement.
  • the color tone of the zirconia powder composition layer (molded body layer) contained in the molded body may be different from that of the sintered body (sintered body layer) obtained by sintering the zirconia powder composition layer. It doesn't have to be.
  • the compact and each powder layer are opaque and have a total light transmittance of 0%. Considering measurement errors, the total light transmittance is 0% or more and 0.2% or less.
  • the compact should have enough strength to prevent cracking or chipping during calcination or sintering.
  • a compact is obtained by layering the powder composition and molding it.
  • Each powder composition is obtained by mixing zirconia powder and a binder, if any, in any desired ratio by a known method.
  • the molding is preferably pressure molding.
  • a mold is filled with a powder composition having a composition corresponding to the bottom layer to form the bottom layer.
  • a powder composition having a composition corresponding to the composition of the layer adjacent to the bottom layer is then filled over the bottom layer.
  • the same operation may be repeated to laminate necessary powder compositions.
  • uniaxial pressure molding is performed at an arbitrary pressure to obtain a preform, which is subjected to CIP treatment to obtain a formed article. During lamination, it is not necessary to apply vibration such as vibration using a vibrator to form a mixed layer between layers.
  • uniaxial pressure molding is preferably performed after filling the powder composition having a composition corresponding to the uppermost layer, and pressure before filling the powder composition having a composition corresponding to the uppermost layer is not performed. preferable.
  • the molding pressure for uniaxial pressure molding is preferably 15 MPa or more and 200 MPa or less, more preferably 18 MPa or more and 100 MPa or less. In uniaxial pressure molding, warpage of the molded body tends to be suppressed as the molding pressure increases.
  • the pressure of the CIP treatment may be a molding pressure of 98 MPa or more and 392 MPa or less.
  • the molded body By treating the molded body at a temperature lower than the sintering temperature, the molded body becomes a calcined body.
  • a known method can be used for the calcining method and calcining conditions.
  • the holding temperature during calcination (hereinafter also referred to as "calcination temperature”) has a lower limit of 800 ° C. or higher, 900 ° C. or higher, or 950 ° C. or higher, and an upper limit of 1200 ° C. or lower, 1150 ° C. or lower, or 1100° C. or lower can be mentioned. Any combination of these upper and lower limits may be used. Therefore, the calcination temperature is, for example, 800° C. or higher and lower than 1200° C., preferably 900° C.
  • the holding time at the calcining temperature (hereinafter also referred to as "calcining time") may be appropriately set depending on the size of the compact to be calcined and the characteristics of the calcining furnace, but the lower limit is preferably 0. 0.5 hours or more, more preferably 0.5 hours or more, and the upper limit is preferably 5 hours or less, more preferably 3 hours or less. Any combination of these upper and lower limits may be used. Therefore, the calcination time is, for example, 0.5 hours or more and 5 hours or less, or 0.5 hours or more and 3 hours or less.
  • the temperature may be raised by dividing the temperature to be raised, the rate of temperature increase at that time, and the holding time at the raised temperature into a plurality of steps. For example, 15°C/hour from room temperature to 300°C, hold at 300°C for 5 hours, 15°C/hour from 300°C to 700°C, hold at 700°C for 1 hour, 50°C/hour from 700°C to 1000°C, hold at 1000°C It may be calcined under conditions such as holding for 2 hours at .
  • the atmosphere in the calcination step (hereinafter also referred to as “calcination atmosphere”) is preferably an atmosphere other than a reducing atmosphere, more preferably at least one of an oxygen atmosphere and an air atmosphere. It is even more preferable to have
  • either a molded body or a calcined body (hereinafter collectively referred to as a "molded body, etc.") is treated at 1200° C. or higher and 1600° C. or lower.
  • the molded body or the like becomes a sintered body.
  • the compact or the like Prior to sintering, the compact or the like may be processed into an arbitrary shape.
  • a known method can be used for the sintering method and sintering conditions. At least one selected from the group of pressureless sintering, HIP treatment, SPS and vacuum sintering can be used as the sintering method.
  • the sintering method is preferably normal pressure sintering, more preferably normal pressure sintering in an air atmosphere.
  • the sintering method is preferably normal pressure sintering only, and more preferably pressure sintering after normal pressure sintering is not performed.
  • pressureless sintering is a method of sintering by simply heating without applying an external force to the sintered material during sintering.
  • the holding temperature during sintering (hereinafter also referred to as "sintering temperature”) has a lower limit of 1200 ° C. or higher, preferably 1300 ° C. or higher, 1400 ° C. or higher, 1430 ° C. or higher, or 1480 ° C. or higher.
  • the upper limit is 1650°C or less, preferably 1580°C or less, 1560°C or less, 1560°C or less, or 1560°C or less. Any combination of these upper and lower limits may be used.
  • the sintering temperature is, for example, 1200°C to 1650°C, 1300°C to 1580°C, 1400°C to 1560°C, 1430°C to 1560°C, or 1480°C to 1560°C.
  • the sintering temperature is 1450°C to 1650°C, preferably 1500°C to 1650°C, more preferably 1550°C to 1650°C.
  • the heating rate up to the sintering temperature has a lower limit of 50° C./hour or more, 100° C./hour or more or 150° C./hour or more, and an upper limit of 800° C./hour or less or 700° C./hour. It is below. Any combination of these upper and lower limits may be used.
  • the heating rate to the sintering temperature is, for example, 50°C/hour or more and 800°C/hour or less, 100°C/hour or more and 800°C/hour or less, 150°C/hour or more and 800°C/hour or less, or 150°C/hour. / hour or more and 700° C./hour or less.
  • the holding time at the sintering temperature (hereinafter also referred to as "sintering time") varies depending on the sintering temperature, the size of the molded body, and the characteristics of the sintering furnace, but preferably the lower limit is 1 hour.
  • the upper limit is 5 hours or less, 3 hours or less, or 2 hours or less. Any combination of these upper and lower limits may be used.
  • the sintering time is, for example, 1 hour or more and 5 hours or less, more preferably 1 hour or more and 3 hours or less, and still more preferably 1 hour or more and 2 hours or less.
  • sintering may be performed under conditions such as from room temperature to 1500° C. at 100° C./hour and holding at 1500° C. for 2 hours.
  • the sintering atmosphere (hereinafter also referred to as “sintering atmosphere”) is preferably an atmosphere other than a reducing atmosphere, more preferably at least one of an oxygen atmosphere and an air atmosphere, and is an air atmosphere. is more preferred.
  • the air atmosphere is mainly composed of nitrogen and oxygen, and can be exemplified by an oxygen concentration of about 18 to 23% by volume.
  • Preferable sintering conditions in the sintering step include normal pressure sintering in an air atmosphere.
  • BET specific surface area The BET specific surface area was measured by the BET 5-point method according to JIS R 1626 using an automatic specific surface area measuring device (device name: Tristar II 3020, manufactured by Shimadzu Corporation). The measurement conditions are as follows. Adsorption medium: N2 Adsorption temperature: -196°C Pretreatment conditions: Air atmosphere, degassing treatment at 250°C for 1 hour or longer
  • the average granule diameter was measured by particle size distribution measurement by a laser diffraction/scattering method using a Microtrac particle size distribution meter (device name: MT3100II, manufactured by Microtrac Bell).
  • the measurement conditions are as follows.
  • Light source semiconductor laser (wavelength: 780 nm)
  • the granulated powder was sieved through a sieve with an opening of 125 ⁇ m, and the granulated powder that passed through the sieve was measured.
  • a disk-shaped molded body, a calcined body, or a sintered body was used as a measurement sample, and the deformation amount of each was obtained from the following formula (3).
  • Amount of deformation (warp: mm) / (dimension: mm) x 100 (3)
  • FIG. 8 schematically shows a molding process of uniaxial press molding in the production of the laminate
  • FIG. 9 schematically shows a molding process of CIP treatment.
  • the powder composition (81) is put into the mold (82) ⁇
  • the powder composition is leveled ⁇
  • the second layer is formed in the same manner, and is repeated thereafter.
  • (d) shows how the powder composition is pressed in uniaxial press molding (83).
  • the uniaxially pressed powder (laminate) (91) is placed in a high-pressure container, the high-pressure container is filled with a solvent (92), and the powder is isotropically pressurized (CIP treatment). show.
  • the measurement of warpage was performed for each laminate of the molded body, the calcined body, and the sintered body by the measurement method shown in FIG.
  • the measurement sample was placed so that the convex portion of the measurement sample was in contact with the horizontal plate.
  • a gauge (product name: 75A19, manufactured by Nagai Gauge Mfg. Co., Ltd.) was inserted into the gap formed between the horizontal plate and the bottom surface to measure warpage.
  • a gauge placed parallel to the horizontal plate is inserted into the gap formed between the horizontal plate and the bottom surface of the sample to be measured, and the maximum thickness of the gauge that can be inserted into the gap is measured.
  • the gauge thickness was taken as the warpage.
  • the warpage was measured sequentially from a gauge thickness of 0.03 mm in increments of 0.01 mm by using a single gauge or a combination of gauges.
  • the dimensions of the measurement sample were obtained by measuring the diameter of the upper end and the diameter of the lower end at four points each using vernier calipers, and obtaining the average value of the diameters of the upper and lower ends.
  • zirconia powder A1 A commercially available zirconia powder Zpex Smile (manufactured by TOSOH) was used as the zirconia powder A1.
  • Zirconia powder A1 was subjected to uniaxial press molding at a pressure of 49 MPa and CIP treatment at a pressure of 196 MPa to obtain a powder layer (molding layer) of zirconia powder A1.
  • a zirconia layer (sintered layer) was obtained by calcining and sintering the obtained powder layer (molded layer) under the following conditions.
  • [Conditions of calcination and sintering] Calcination: 15°C/hour from room temperature to 300°C, held at 300°C for 5 hours, 15°C/hour from 300°C to 700°C, held at 700°C for 1 hour, 50°C/hour from 700°C to 1000°C, 1000 C. for 2 hours and then cooled in the furnace.
  • Sintering from room temperature to 1500°C at 100°C/hour, held at 1500°C for 2 hours, and then cooled in the furnace.
  • the color tone was measured using a calorimeter (apparatus name: ZE6000, manufactured by Nippon Denshoku Industries Co., Ltd.).
  • the measurement conditions are as follows.
  • As specific measurement conditions for color tone and C * a method of placing a zero calibration box on a measurement sample (so-called black background measurement) for measurement was performed under the following conditions.
  • Light source D65 light source
  • Viewing angle 2°
  • Measurement method SCI
  • SCI For the sintered body sample, after cutting out an arbitrary part of the sintered body in the horizontal direction, the measurement surface of the sample was mirror-polished, and the sample thickness was 2.8 ⁇ 0.1 mm and the surface roughness (Ra) was 0. 02 ⁇ m or less.
  • Table 1-2 shows the evaluation results of the properties of the zirconia layer (sintered body layer) using the zirconia powder A1.
  • This is mixed with ⁇ -alumina, iron oxide as an oxide coloring element, and pure water to form a slurry, which is treated with a ball mill for 22 hours to obtain 0.05% by mass of alumina and iron oxide as an oxide coloring element.
  • a slurry containing powder containing 0.085% by mass of iron in terms of conversion and the balance being zirconia containing 5.05 mol% yttrium and 0.15 mol% erbium was obtained.
  • An acrylic binder was added to and mixed with the obtained slurry so that the mass ratio of the binder to the mass of the powder in the slurry was 3% by mass.
  • the slurry was spray-dried at 180° C. in air to obtain zirconia powder A2.
  • the obtained zirconia powder had a BET specific surface area of 10.1 m 2 /g and an average particle size of 44 ⁇ m.
  • Zirconia powder A3 to A6 In the same manner as zirconia powder A2, except that it was fired at 1130 ° C. and that yttrium chloride, erbium oxide ⁇ -alumina, and iron oxide were used to have the compositions shown in Table 1-1, respectively, Zirconia powders A3 to A6 were obtained. The compositions of zirconia powders A1 to A6 are shown in Table 1-1.
  • a zirconia layer (sintered body layer) was produced using each of the zirconia powders A2 to A6 by the same method as described in the section (Zirconia powder A1) above, and the properties of the zirconia layer (sintered body layer) were measured. evaluated. Evaluation results are shown in Table 1-2.
  • Zirconia powder B1 A commercially available zirconia powder Zpex4 (manufactured by TOSOH) was used as the zirconia powder B1.
  • zirconia powder C1 A commercially available zirconia powder Zpex (manufactured by TOSOH) was used as the zirconia powder C1.
  • Zirconia powder B8 to B11 Zirconia powder except that it was fired at 1125 ° C. and that yttrium chloride, erbium oxide, ⁇ -alumina, iron oxide, tricobalt tetraoxide and titanium oxide were used to achieve the compositions shown in Table 1-1.
  • Zirconia powders B8 to B11 were produced in the same manner as A2.
  • sintered layers were produced using these powders, and the properties of the sintered layers were evaluated. Evaluation results are shown in Table 1-2. Incidentally, ppm in Table 1-2 is mass ppm.
  • the sample layer was produced by the molding process shown in FIGS. 3 and 4 as described above.
  • a sample layer of the molded body layer composed of the obtained powder layer (powder composition layer) was calcined under the following conditions to obtain a sample layer of the zirconia composition layer (calcined body layer).
  • the sample layer of the zirconia composition layer (calcined body layer) was sintered under the following conditions to obtain a sample layer of the zirconia layer (sintered body layer).
  • the shrinkage rate was measured for each sample layer obtained as described above.
  • the diameter of the shrinkage measurement sample (hereinafter also referred to as "sample diameter") was measured with a caliper.
  • the sample diameter was determined by measuring the diameter of each sample for contraction rate measurement at four points using a vernier caliper, and taking the average value of the measured values as the sample diameter.
  • the shrinkage ratio was calculated from the following formula (1).
  • ⁇ Shrinkage rate (%) ⁇ (mold diameter: ⁇ 25mm - sample diameter) / mold diameter: ⁇ 25mm ⁇ x 100 (1)
  • a powder layer (molded body layer), a zirconia composition layer (calcined body layer), and a zirconia layer (sintered body Table 2 shows the measurement results of the shrinkage rate of each sample layer.
  • Example 1 (Molded body) After filling a mold with an inner diameter of 110 mm with an amount (21 g) of zirconia powder A1 that will give a layer thickness of 1 mm when calcined, the mold is tapped to form the (i)-th powder layer ( corresponding to the first layer (21)). After filling the amount (214 g) of zirconia powder A2 that makes the layer thickness of the calcined body 10 mm on the (i)-th powder layer, the mold is tapped to form the (ii)-th powder layer ( (corresponding to the third layer (23) in FIG. 2).
  • the filling material of the (i)th powder layer to the (iv)th powder layer was subjected to uniaxial pressure press molding at a pressure of 98 MPa. After that, a CIP treatment was performed at a pressure of 196 MPa to obtain a four-layer laminate, which was used as a compact according to this example.
  • the molded body was calcined under the following calcination conditions to obtain a laminate, which was used as a calcined body according to the present example.
  • [Pre-firing conditions] Calcination: 15°C/hour from room temperature to 300°C, hold at 300°C for 5 hours, 15°C/hour from 300°C to 700°C, hold at 700°C for 1 hour, 50°C/hour from 700°C to 1000°C, 1000 C. for 2 hours and then cooled in the furnace.
  • the calcined body was fired under the following sintering conditions to obtain a laminated body, which was used as a sintered body according to this example.
  • [Sintering conditions] Sintering: from room temperature to 1500°C at 100°C/hour, held at 1500°C for 2 hours, and then cooled in the furnace.
  • Table 3-1 shows the types of powders used in Example 1, the order of powder stacking, and the conditions of Example 1, and Table 3-2-1 shows the evaluation results.
  • the warp measurement result of the sintered body of Example 1 was less than the measurement limit (0.03 mm).
  • Table 3-2-1 and Table 3-2-2 are collectively referred to as Table 3-2.
  • Example 2 A laminate shown in Table 3-1 was produced in the same manner as in Example 1 except that the type of powder used and the order of lamination of the powder used were changed as shown in Table 3-1 with respect to Example 1. did.
  • the evaluation results are shown in Table 3-2 below.
  • the measurement result of warpage described as “less than 0.03 mm” means that the measurement limit is less than 0.03 mm, and the amount of deformation is "less than 0.03 mm" in the forming and calcining columns. means a measurement limit of less than 0.03 mm, and "less than 0.04 mm” in the sintering column of the deformation amount means a measurement limit of less than 0.04 mm.
  • the content of the stabilizing element to be a close value (specifically, 2.0 mol% or less)
  • the warp of the sintered body can be suppressed, and the translucency and color tone close to those of natural teeth can be obtained. It was found that a sintered body having gradation and little deformation can be produced.
  • the first region eg, the bottom layer located at one end of the laminate and the second region (eg, the top layer) located at the other end
  • the shrinkage rate of the sintered body to a value close to (specifically, 0.4% or less)
  • the warp of the sintered body can be suppressed, and the translucency and color gradation close to natural teeth can be achieved. It was found that a sintered body with less deformation can be produced while having the
  • the entire contents of the specification, claims, drawings and abstract of Japanese Patent Application No. 2022-024064 filed on February 18, 2022 are cited here, and the specification of the present disclosure is Incorporate as a disclosure.

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US18/838,733 US20250197294A1 (en) 2022-02-18 2023-02-16 Calcined body and sintered body of zirconia
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EP23756448.9A EP4480935A4 (en) 2022-02-18 2023-02-16 CALCINED OBJECT AND SINTERED OBJECT BASED ON ZIRCONIA
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CN117263717A (zh) * 2023-09-27 2023-12-22 先导薄膜材料(淄博)有限公司 一种未完全烧结的氧化锆陶瓷板及其制备方法

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