Alumina sintered body and manufacturing method therefor

Abstract

The present invention relates to an alumina sintered body and a manufacturing method therefor; for example, the present invention relates to an alumina sintered body that is suitably utilized for a member or similar used in a plasma processing device, an etcher for semiconductor/liquid crystal display device manufacturing, a CVD device, or similar, or that is suitably utilized for a substrate or similar of a plasma-resistant member which is to be coated, as well as a manufacturing method for said alumina sintered body.

Claims

1. An alumina-based sintered object having an Al content, in terms of Al.sub.2O.sub.3 content, of 99.8 wt % or higher, wherein the alumina-based sintered object has an Si content, in terms of SiO.sub.2 content, of 321 ppm to 600 ppm and an Na content, in terms of Na.sub.2O content, of more than zero and 27 ppm or less, and wherein the alumina-based sintered object has a density of 3.96 g/cm.sup.3 or higher and an average pore diameter of 5 μm or less.

2. The alumina-based sintered object according to claim 1, containing Mg in an amount which, in terms of MgO content, is 1.0 to 4.0 times the Si content in terms of SiO.sub.2 content.

3. The alumina-based sintered object according to claim 1, containing Ca in an amount which, in terms of CaO content, is up to 3.0 times the Si content in terms of SiO.sub.2 content.

4. The alumina-based sintered object according to claim 1, wherein Al.sub.2O.sub.3 crystals contained in the alumina-based sintered object have an average crystal grain diameter of 3 μm to 40 μm.

5. The alumina-based sintered object according to claim 1, wherein a corrosion-resistant film or a corrosion-resistant layer is formed on at least a part of the alumina-based sintered object.

6. The alumina-based sintered object according to claim 1, wherein the alumina-based sintered object has a surface roughness Ra of less than 0.1 μm.

7. The alumina-based sintered object according to claim 1, wherein the Na content, in terms of the Na.sub.2O content, is in a range from 2 ppm to 27 ppm.

8. The alumina-based sintered object according to claim 1, wherein the Na content, in terms of the Na.sub.2O content, is in a range from 10 ppm to 27 ppm.

9. A process for producing the alumina-based sintered object according to claim 4, the process comprising: granulating and molding a raw-material powder to obtain a molded object, and firing the molded object in a hydrogen atmosphere at 1,600° C. to 1,900° C.

Description

BRIEF DESCRIPTION OF DRAWINGS

(1) FIG. 1 shows a photograph of a cross-section obtained in Example 1A.

DESCRIPTION OF EMBODIMENTS

(2) The alumina-based sintered object of a first embodiment according to the first aspect of the present invention is explained below.

(3) The alumina-based sintered object according to the first embodiment is an alumina-based sintered object having an Al content, in terms of Al.sub.2O.sub.3 content, of 70% by weight or higher, in which the alumina-based sintered object has a Zr content, in terms of ZrO.sub.2 content, of 30% by weight or less, an Si content, in terms of SiO.sub.2 content, of 170 ppm to 600 ppm, and an Na content, in terms of Na.sub.2O content, of 27 ppm or less.

(4) This alumina-based sintered object has high flexural strength, has both corrosion resistance and low-dielectric-loss characteristics, and serves as a substrate on which an even and dense film can be deposited.

(5) This alumina-based sintered object has an Al content, in terms of Al.sub.2O.sub.3 content, of 70% by weight or higher and has a Zr content, in terms of ZrO.sub.2 content, of 30% by weight or less.

(6) In this alumina-based sintered object, a ZrO.sub.2 crystal phase has been formed besides the main crystals of Al.sub.2O.sub.3. This ZrO.sub.2 crystal phase not only contributes to a reduction in the amount of pores but also is inhibited from undergoing abnormal grain growth and has a reduced grain diameter. The ZrO.sub.2 crystal phase hence serves to enhance the strength.

(7) However, in case where the Zr content in terms of ZrO.sub.2 content exceeds 30% by weight, the Al content in terms of Al.sub.2O.sub.3 content is less than 70% by weight and this alumina-based sintered object does not have high resistance to corrosion by highly reactive halogen-based corrosive gases or plasmas thereof. Such Zr contents are hence undesirable.

(8) In addition, in case where the Zr content in terms of ZrO.sub.2 content exceeds 30% by weight, the ZrO.sub.2 crystal phase is present in an increased amount and this results in a decrease in the strength of the alumina-based sintered object. Furthermore, the dielectric loss tangent tan δ exceeds 10.sup.−3. Such Zr contents are hence undesirable.

(9) Consequently, the Al content in terms of Al.sub.2O.sub.3 content is 70% by weight or higher, and the Zr content in terms of ZrO.sub.2 content is 30% by weight or less.

(10) Any ingredients contained in the alumina-based sintered object other than Al.sub.2O.sub.3 and ZrO.sub.2 are substances which have unavoidably come into the alumina in the steps for alumina production. Examples thereof include Si, Mg, Na, and Ca.

(11) In this alumina-based sintered object, the Si content in terms of SiO.sub.2 content is 170 ppm to 600 ppm.

(12) In case where the Si content in terms of SiO.sub.2 content is less than 170 ppm, silicates which are necessary for imparting low-dielectric-loss characteristics are not evenly formed, resulting in an increase in dielectric loss and making it impossible to obtain the effect of power saving. Such Si contents are hence undesirable.

(13) Meanwhile, in case where the Si content in terms of SiO.sub.2 content exceeds 600 ppm, this alumina-based sintered object has a low density and is not dense. Such Si contents are hence undesirable.

(14) In the alumina-based sintered object according to the first embodiment, the Na content in terms of Na.sub.2O content is 27 ppm or less. In case where the Na content in terms of Na.sub.2O content exceeds 27 ppm, this alumina-based sintered object has an increased dielectric loss and does not have the effect of power saving. Such Na contents are hence undesirable.

(15) It is preferable that, in the alumina-based sintered object according to the first embodiment, the content of Mg, in terms of MgO content, is 1.0 to 4.0 times the Si content in terms of SiO.sub.2 content.

(16) In cases when the content of Mg, in terms of MgO content, is 1.0 to 4.0 times the Si content in terms of SiO.sub.2 content, silicates can be formed at grain boundaries of the alumina-based sintered object. Hence, an alumina-based sintered object having a high density and a low dielectric loss can be obtained.

(17) It is preferable that in the alumina-based sintered object according to the first embodiment, the content of Ca, in terms of CaO content, is up to 3.0 times the Si content in terms of SiO.sub.2 content.

(18) In cases when the content of Ca, in terms of CaO content, is up to 3.0 times the Si content in terms of SiO.sub.2 content, silicates can be formed at grain boundaries. Hence, an alumina-based sintered object having a low dielectric loss can be obtained.

(19) It is preferable that, in the alumina-based sintered object according to the first embodiment, the Al.sub.2O.sub.3 crystals have an average crystal grain diameter of 3 μm to 15 μm.

(20) In cases when the Al.sub.2O.sub.3 crystals contained in the alumina-based sintered object have an average crystal grain diameter of 3 μm to 15 μm, this alumina-based sintered object can be made to have a smaller amount of pores. It is hence possible to obtain a sintered object having a higher density and to obtain an alumina-based sintered object having a three-point bending strength of 320 MPa or higher.

(21) It is preferable that the alumina-based sintered object according to the first embodiment has a water absorption of 0.2% or less. The water absorption is the smaller, the porosity of the alumina-based sintered object is smaller. Thus the smaller the water absorption is, the denser the alumina-based sintered object is.

(22) Consequently, a thin film can be evenly formed on the surface of the alumina-based sintered object having a water absorption of 0.2% or less.

(23) It is preferable that the alumina-based sintered object according to the first embodiment has an average pore diameter of 5 μm or less. In cases when the alumina-based sintered object has an average pore diameter of 5 μm or less, a thin film can be more evenly formed on the surface of the alumina-based sintered object.

(24) Although the alumina-based sintered object according to the first embodiment may be used as such, the alumina-based sintered object may be used after a dense film is formed on a surface thereof.

(25) The film is obtained, for example, by depositing a film of an yttria material on the alumina-based sintered object using an aerosol deposition method or PVD. The alumina-based sintered object on which a film of an yttria material has been thus deposited has high plasma resistance, is highly inhibited from causing dusting, and is capable of attaining power saving, etc. due to the low-dielectric-loss characteristics of the substrate.

(26) As stated above, in cases when the alumina-based sintered object has a water absorption of 0.2% or less, a thin film can be evenly formed on the surface of this alumina-based sintered object.

(27) Especially in the case where the alumina-based sintered object has an average pore diameter of 5 μm or less, a thin film of yttria can be more evenly deposited on the surface of the alumina-based sintered object.

(28) The film to be formed on the surface of the alumina-based sintered object is not limited to yttria materials. For example, the film may be any of: a composite oxide (YAG) including yttrium oxide and aluminum oxide; erbium oxide; oxides of other rare earth elements; and composite oxides including oxides of rare earth elements.

(29) It is desirable that the surface of the alumina-based sintered object on which a film is to be formed has a surface roughness Ra of less than 0.1 μm. The surface of the alumina-based sintered object may be mirror-polished before film formation, thereby reducing the surface roughness to less than 0.1 pun. Namely, it is desirable that the surface of the alumina-based sintered object on which a film is to be formed has an average pore diameter of 5 μm or less and a surface roughness Ra of less than 0.1 μm.

(30) On the alumina-based sintered object having such a surface, a thin film can be more evenly formed. This thin film is inhibited from peeling off, and particle generation can be inhibited.

(31) The film to be formed on the alumina-based sintered object may be one to be formed on a part of the surface of the alumina-based sintered object. The thickness of the film is not particularly limited. However, the thickness thereof is preferably 1 μm to 20 μm.

(32) The alumina-based sintered object can be produced by a process generally used for producing an alumina-based sintered object. For example, the alumina-based sintered object can be produced by the following process.

(33) First, a ZrO.sub.2 powder or an aqueous solution thereof is added to an Al.sub.2O.sub.3 powder having a predetermined median diameter. A binder or the like (e.g., PVA) is added thereto to prepare a raw-material powder. This raw-material powder is stirred and mixed by a mixer to obtain a raw-material slurry, which is then granulated.

(34) The resultant granules are molded to thereby produce a molded object. For the molding, use can be made of various methods such as uniaxial press molding, CIP molding, wet molding, and pressure casting.

(35) The molded object is fired at a temperature in the range of 1,600° C. to 1,900° C. for 6 hours or longer in a hydrogen atmosphere, thereby obtaining the alumina-based sintered object.

(36) By thus firing the molded object at 1,600° C. to 1,900° C. in a hydrogen atmosphere, an alumina-based sintered object having a high density can be obtained.

(37) Next, the alumina-based sintered object of a second embodiment according to the second aspect of the present invention is explained.

(38) The alumina-based sintered object according to the second embodiment is an alumina-based sintered object having an Al content, in terms of Al.sub.2O.sub.3 content, of 70% by weight or higher, in which the alumina-based sintered object has a Zr content, in terms of ZrO.sub.2 content, of 30% by weight or less, a Y content, in terms of Y.sub.2O.sub.3 content, of 1% to 10% by weight, an Si content, in terms of SiO.sub.2 content, of 170 ppm to 600 ppm, and an Na content, in terms of Na.sub.2O content, of 27 ppm or less, and the Y content, in terms of Y.sub.2O.sub.3 content, is not more than the Zr content, in terms of ZrO.sub.2 content.

(39) The alumina-based sintered object according to the second embodiment has high flexural strength, has both corrosion resistance and low-dielectric-loss characteristics, and serves as a substrate on which an even and dense film can be deposited.

(40) In the alumina-based sintered object according to the second embodiment, the content of Al, in terms of Al.sub.2O.sub.3 content, is 70% by weight or higher. The content of Zr therein, in terms of ZrO.sub.2 content, is 30% by weight or less, and the content of Y therein, in terms of Y.sub.2O.sub.3 content, is 1% to 10% by weight.

(41) In the alumina-based sintered object according to the second embodiment, a ZrO.sub.2 crystal phase has been formed besides the main crystals of Al.sub.2O.sub.3. The ZrO.sub.2 crystal phase not only contributes to a reduction in the amount of pores but also is inhibited from undergoing abnormal grain growth and has a reduced grain diameter. The ZrO.sub.2 crystal phase hence serves to enhance the strength.

(42) However, in case where the Zr content in terms of ZrO.sub.2 content exceeds 30% by weight, the Al content in terms of Al.sub.2O.sub.3 content is less than 70% by weight and this alumina-based sintered object does not have high resistance to corrosion by highly reactive halogen-based corrosive gases or plasmas thereof. Such Zr contents are hence undesirable.

(43) In addition, in case where the Zr content in terms of ZrO.sub.2 content exceeds 30% by weight, the ZrO.sub.2 crystal phase is present in an increased amount and this results in a decrease in the strength of the alumina-based sintered object. Furthermore, the dielectric loss tangent tan δ exceeds 10.sup.−3. Such Zr contents are hence undesirable.

(44) Consequently, the Al content in terms of Al.sub.2O.sub.3 content is 70% by weight or higher, and the Zr content in terms of ZrO.sub.2 content is 30% by weight or less.

(45) Furthermore, in this embodiment, the content of Y, in terms of Y.sub.2O.sub.3 content, is 1% to 10% by weight.

(46) In cases when the Zr addition amount is large, this alumina-based sintered object may crack due to the influence of phase transition. Yttrium has the effect of inhibiting the cracking due to the addition of Zr.

(47) With respect to the addition amount of Y, in case where the content of Y, in terms of Y.sub.2O.sub.3 content, is less than 1% by weight, the effect of cracking inhibition is too low. In case where Y is added in an amount exceeding 10% by weight, some of the Y reacts with Al.sub.2O.sub.3 during the firing step to yield YAG. In case where the YAG is present in too large an amount, the alumina-based sintered object has a reduced three-point bending strength. The content of Y is hence 10% by weight or less.

(48) In addition, in case where the content of Y, in terms of Y.sub.2O.sub.3 content, is more than the content of Zr, in terms of ZrO.sub.2 content, the alumina-based sintered object has a reduced three-point bending strength, and hence it is not preferable. Therefore, it is preferable that the content of Y, in terms of Y.sub.2O.sub.3 content, is not more than the content of Zr, in terms of ZrO.sub.2 content.

(49) Any ingredients contained in the alumina-based sintered object according to the second embodiment other than Al.sub.2O.sub.3, ZrO.sub.2, and Y.sub.2O.sub.3 are substances which have unavoidably come into the alumina in the steps for alumina production, as in the first embodiment. Examples thereof include Si, Mg, Na, and Ca.

(50) As in the first embodiment, the content of Si, in terms of SiO.sub.2 content, in this alumina-based sintered object is 170 ppm to 600 ppm. The content of Na therein, in terms of Na.sub.2O content, is 27 ppm or less. It is preferable that the content of Mg, in terms of MgO content, is 1.0 to 4.0 times the Si content in terms of SiO.sub.2 content.

(51) Furthermore, it is preferable that the content of Ca, in terms of CaO content, is up to 3.0 times the Si content in terms of SiO.sub.2 content.

(52) It is preferable that the Al.sub.2O.sub.3 crystals contained in the alumina-based sintered object according to the second embodiment have an average crystal grain diameter of 3 μm to 15 μm, as in the first embodiment.

(53) It is preferable that the alumina-based sintered object according to the second embodiment has a water absorption of 0.2% or less, as in the first embodiment.

(54) It is preferable that this alumina-based sintered object has an average pore diameter of 5 μm or less.

(55) Although the alumina-based sintered object according to the second embodiment may be used as such, the alumina-based sintered object may be used after a dense film is formed on a surface thereof, as in the first embodiment.

(56) The film is obtained, for example, by depositing a film of an yttria material on the alumina-based sintered object using an aerosol deposition method or PVD, as in the first embodiment.

(57) As stated above, in cases when the alumina-based sintered object has a water absorption of 0.2% or less, a thin film can be evenly formed on the surface of this alumina-based sintered object.

(58) Especially in the case where the alumina-based sintered object has an average pore diameter of 5 μm or less, a thin film of yttria can be more evenly deposited on the surface of the alumina-based sintered object.

(59) The film to be formed on the surface of the alumina-based sintered object is not limited to yttria materials. For example, the film may be any of: a composite oxide (YAG) including yttrium oxide and aluminum oxide; erbium oxide; oxides of other rare earth elements; and composite oxides including oxides of rare earth elements.

(60) It is desirable that the surface of the alumina-based sintered object on which a film is to be formed has a surface roughness Ra of less than 0.1 μm, as in the first embodiment. The surface of the alumina-based sintered object may be mirror-polished before film formation, thereby reducing the surface roughness to less than 0.1 μm. Namely, it is desirable that the surface of the alumina-based sintered object on which a film is to be formed has an average pore diameter of 5 μm or less and a surface roughness Ra of less than 0.1 μm.

(61) On the alumina-based sintered object having such a surface, a thin film can be more evenly formed. This thin film is inhibited from peeling off, and particle generation can be inhibited.

(62) The film to be formed on the alumina-based sintered object may be one to be formed on a part of the surface of the alumina-based sintered object. The thickness of the film is not particularly limited. However, the thickness thereof is preferably 1 μm to 20 μm.

(63) The alumina-based sintered object can be produced by a process generally used for producing an alumina-based sintered object, as stated above with regard to the first embodiment. For example, the alumina-based sintered object can be produced by the following process.

(64) First, either a ZrO.sub.2 powder and a Y.sub.2O.sub.3 powder or an aqueous solution of these is added to an Al.sub.2O.sub.3 powder having a predetermined median diameter. A binder or the like (e.g., PVA) is added thereto to prepare a raw-material powder. This raw-material powder is stirred and mixed by a mixer to obtain a raw-material slurry, which is then granulated.

(65) The resultant granules are molded to thereby produce a molded object. For the molding, use can be made of various methods such as uniaxial press molding, CIP molding, wet molding, and pressure casting.

(66) The molded object is fired at a temperature in the range of 1,600° C. to 1,900° C. for 6 hours or longer in a hydrogen atmosphere, thereby obtaining the alumina-based sintered object.

(67) By thus firing the molded object at 1,600° C. to 1,900° C. in a hydrogen atmosphere, an alumina-based sintered object having a three-point bending strength of 320 MPa or higher, including Al.sub.2O.sub.3 crystals with an average crystal grain diameter of 3 μm to 15 μm, and having a water absorption of 0.2% or less is obtained. This alumina-based sintered object can be obtained as an alumina-based sintered object which has such low-dielectric-loss characteristics that the value of the dielectric loss tangent tan δ at 10 MHz to 20 MHz is 10.sup.−3 or less.

(68) The alumina-based sintered object of a third embodiment according to the third aspect of the present invention is explained.

(69) The alumina-based sintered object according to the third embodiment is an alumina-based sintered object having an Al content, in terms of Al.sub.2O.sub.3 content, of 99.8 wt % or higher, in which the alumina-based sintered object has an Si content, in terms of SiO.sub.2 content, of 170 ppm to 600 ppm and an Na content, in terms of Na.sub.2O content, of 27 ppm or less, and the alumina-based sintered object has a density of 3.96 g/cm.sup.3 or higher.

(70) The alumina-based sintered object according to the third embodiment has both corrosion resistance and low-dielectric-loss characteristics and serves as a substrate on which an even and dense film can be deposited.

(71) The alumina-based sintered object according to the third embodiment has an Al content, in terms of Al.sub.2O.sub.3 content, of 99.8 wt % or higher. In case where the content of Al in terms of Al.sub.2O.sub.3 content is less than 99.8 wt %, this alumina-based sintered object does not have high resistance to corrosion by highly reactive halogen-based corrosive gases or plasmas thereof. Such Al contents are hence undesirable.

(72) Any ingredients contained in the alumina-based sintered object according to the third embodiment other than Al.sub.2O.sub.3 are substances which have unavoidably come into the alumina in the steps for alumina production. Examples thereof include Si, Mg, Na, and Ca.

(73) In the alumina-based sintered object according to the third embodiment, the Si content in terms of SiO.sub.2 content is 170 ppm to 600 ppm.

(74) In case where the Si content in terms of SiO.sub.2 content is less than 170 ppm, silicates which are necessary for imparting low-dielectric-loss characteristics are not evenly formed, resulting in an increase in dielectric loss and making it impossible to obtain the effect of power saving. Such Si contents are hence undesirable.

(75) Meanwhile, in case where the Si content in terms of SiO.sub.2 content exceeds 600 ppm, this alumina-based sintered object has a low density and is not dense. Such Si contents are hence undesirable.

(76) Specifically, the density of the alumina-based sintered object according to the third embodiment is 3.96 g/cm.sup.3 or higher.

(77) In the alumina-based sintered object according to the third embodiment, the Na content in terms of Na.sub.2O content is 27 ppm or less. In case where the Na content in terms of Na.sub.2O content exceeds 27 ppm, this alumina-based sintered object has an increased dielectric loss and does not have the effect of power saving. Such Na contents are hence undesirable.

(78) It is preferable that, in the alumina-based sintered object according to the third embodiment, the content of Mg, in terms of MgO content, is 1.0 to 4.0 times the Si content in terms of SiO.sub.2 content.

(79) In cases when the content of Mg, in terms of MgO content, is 1.0 to 4.0 times the Si content in terms of SiO.sub.2 content, silicates can be formed at grain boundaries of the alumina-based sintered object. Hence, an alumina-based sintered object having a high density and a low dielectric loss can be obtained.

(80) It is preferable that, in the alumina-based sintered object according to the third embodiment, the content of Ca, in terms of CaO content, is up to 3.0 times the Si content in terms of SiO.sub.2 content.

(81) In cases when the content of Ca, in terms of CaO content, is up to 3.0 times the Si content in terms of SiO.sub.2 content, silicates can be formed at grain boundaries. Hence, an alumina-based sintered object having a low dielectric loss can be obtained.

(82) It is preferable that, in the alumina-based sintered object according to the third embodiment, the Al.sub.2O.sub.3 crystals have an average crystal grain diameter of 3 μm to 40 μm. The average crystal grain diameter thereof is more preferably 10 μm to 25 μm.

(83) In cases when the Al.sub.2O.sub.3 crystals in the alumina-based sintered object have an average crystal grain diameter of 3 μm to 40 μm, this alumina-based sintered object can be made to have a smaller amount of pores. It is hence possible to obtain a sintered object having a higher density and to obtain an alumina-based sintered object having a three-point bending strength of 250 MPa or higher.

(84) It is preferable that the alumina-based sintered object according to the third embodiment has an average pore diameter of 5 μm or less. In cases when the alumina-based sintered object has an average pore diameter of 5 μm or less, a thin film can be evenly formed on the surface of the alumina-based sintered object.

(85) Although the alumina-based sintered object according to the third embodiment may be used as such, the alumina-based sintered object may be used after a dense film is formed on a surface thereof.

(86) The film is obtained, for example, by depositing a film of an yttria material on the alumina-based sintered object using an aerosol deposition method or PVD. The alumina-based sintered object on which a film of an yttria material has been thus deposited has high plasma resistance, is highly inhibited from causing dusting, and is capable of attaining power saving, etc. due to the low-dielectric-loss characteristics of the substrate.

(87) As stated above, in cases when the alumina-based sintered object has an average pore diameter of 5 μm or less, a thin film of yttria can be evenly deposited on the surface of the alumina-based sintered object.

(88) The film to be formed on the surface of the alumina-based sintered object is not limited to yttria materials. For example, the film may be any of: a composite oxide (YAG) including yttrium oxide and aluminum oxide; erbium oxide; oxides of other rare earth elements; and composite oxides including oxides of rare earth elements.

(89) It is desirable that the surface of the alumina-based sintered object on which a film is to be formed has a surface roughness Ra of less than 0.1 μm. The surface of the alumina-based sintered object may be mirror-polished before film formation, thereby reducing the surface roughness to less than 0.1 μm. Namely, it is desirable that the surface of the alumina-based sintered object on which a film is to be formed has an average pore diameter of 5 μm or less and a surface roughness Ra of less than 0.1 μm.

(90) On the alumina-based sintered object having such a surface, a thin film can be more evenly formed. This thin film is inhibited from peeling off, and particle generation can be inhibited.

(91) The film to be formed on the alumina-based sintered object may be one to be formed on a part of the surface of the alumina-based sintered object. The thickness of the film is not particularly limited. However, the thickness thereof is preferably 1 μm to 20 μm.

(92) The alumina-based sintered object can be produced by a process generally used for producing an alumina-based sintered object. For example, the alumina-based sintered object can be produced by the following process.

(93) First, a binder or the like (e.g., PVA) is added to an Al.sub.2O.sub.3 powder having a predetermined median diameter to prepare a raw-material powder. This raw-material powder is stirred and mixed by a mixer to obtain a raw-material slurry, which is then granulated.

(94) The resultant granules are molded to thereby produce a molded object. For the molding, use can be made of various methods such as uniaxial press molding, CIP molding, wet molding, and pressure casting.

(95) The molded object is fired at a temperature in the range of 1,600° C. to 1,900° C. for 6 hours or longer in a hydrogen atmosphere, thereby obtaining the alumina-based sintered object.

(96) By thus firing the molded object at 1,600° C. to 1,900° C. in a hydrogen atmosphere, an alumina-based sintered object having a high density can be obtained.

EXAMPLES

(97) The present invention is explained below in detail by reference to Examples, but the invention should not be construed as being limited by the following Examples.

Experiment 1A

(98) As shown in Table 1, a ZrO.sub.2 powder was added to an alumina powder having a median diameter of 2 μm or less using water as a medium, and PVA was added thereto to prepare a raw-material powder. This raw-material powder was stirred and mixed for 16 hours or longer to obtain a raw-material slurry. This raw-material slurry was granulated, and the granules were packed into a molding die and molded by CIP at a molding pressure of 1.5 tons.

(99) Furthermore, the resultant molded object was subjected to a degreasing step in the air and then fired at 1,600° C. in a hydrogen atmosphere. Thus, samples of Examples 1A to 7A and Comparative Examples 1A to 6A were produced.

(100) SiO.sub.2 and Na.sub.2O were added according to need so as to give sintered objects each having an Si content and an Na content within the ranges according to the present invention.

(101) The samples of Examples 1A to 7A and Comparative Examples 1A to 6A were evaluated for water absorption, average Al.sub.2O.sub.3 crystal grain diameter, dielectric loss tangent tan δ, and three-point bending strength. The results thereof are shown in Table 1.

(102) The average alumina crystal gram diameter was determined by mirror-polishing a cross-section of each sample, subjecting the polished cross-section to thermal etching, subsequently taking a photograph of the cross-section with a scanning electron microscope (SEM), and calculating the average crystal grain diameter by image analysis.

(103) The photograph of the cross-section taken with the scanning electron microscope (SEM) in Example 1A is shown in FIG. 1.

(104) The three-point bending strength was measured in accordance with JIS R 1601:2008. The purity of each sintered object was determined by ICP emission analysis. The dielectric loss tangent tan δ was determined at frequencies of 10 MHz to 20 MHz using an impedance analyzer.

(105) The water absorption was determined by obtaining dry weight W1 and weight in water W2 by the same method as that described in JIS R 1634:1998 and calculating the water absorption using the following equation.
Water absorption (%)=(W2−W1)W1×100

(106) Furthermore, a surface of each of the samples (alumina-based sintered object) of Examples 1A to 7A and Comparative Examples 1A to 6A obtained above was mirror-polished so as to result in Ra<0.1 μm, and the polished surface was coated with an yttrium oxide material in a thickness of 1 μm by the aerosol deposition method.

(107) The deposition material was dried at 270° C. for 12 hours or longer as a pretreatment, and the deposition was then conducted by aerosol jetting under the following conditions:

(108) Sample temperature, room temperature; powder container temperature, 150° C.; raising/conveying gas, He; powder raising rate, 3 L/min; powder conveying rate, 10 L/min; powder collision angle, 60σ; nozzle opening shape, 5×0.3 mm; sample-to-nozzle distance, 5 mm; sample traveling speed, 200 mm/min; number of passes for deposition, 10.

(109) The thus-obtained thin-film-coated samples of Examples 1A to 7A and Comparative Examples 1A to 6A were each examined for surface state over a range of about 200 μm×200 μm using a scanning electron microscope. From the image obtained, the diameters of voids and the number of the voids were determined using an image analysis software. As shown in Table 1, each sample which satisfied the number of voids of 100 or less was regarded as having been coated with an even film and indicated by “A”, and each sample which did not satisfy the requirement was regarded as having been coated with an uneven film and indicated by “B”.

(110) TABLE-US-00001 TABLE 1 Three- Average Al content Zr content Si content Na content point crystal- State of voids in (in terms (in terms (in terms (in terms bending tanδ grain Water thin-film surface: of Al.sub.2O.sub.3) of ZrO.sub.2) of SiO.sub.2) of Na.sub.2O) strength @10 to 20 diameter absorption Number of voids ≤ 100; (wt %) (wt %) (ppm) (ppm) (MPa) MHz (μm) (%) Average diameter ≤ 5 μm Example 1A 90 10 300 10 350 <10.sup.−3 5 ≤0.2 A Example 2A 90 10 300 27 350 <10.sup.−3 5 ≤0.2 A Example 3A 90 10 300 2 350 <10.sup.−3 5 ≤0.2 A Example 4A 90 10 170 10 340 <10.sup.−3 4 ≤0.2 A Example 5A 90 10 600 10 340 <10.sup.−3 6 ≤0.2 A Example 6A 70 30 300 10 320 <10.sup.−3 3 ≤0.2 A Example 7A 99 1 300 10 325 <10.sup.−3 12 ≤0.2 A Comparative 50 50 300 10 250 >10.sup.−3 3 >0.2 B Example 1A Comparative 50 50 800 10 230 >10.sup.−3 3 >0.2 B Example 2A Comparative 90 10 800 10 310 <10.sup.−3 16 >0.2 B Example 3A Comparative 90 10 800 50 310 >10.sup.−3 16 >0.2 B Example 4A Comparative 90 10 5 10 330 >10.sup.−3 5 >0.2 B Example 5A Comparative 90 10 300 50 350 >10.sup.−3 5 ≤0.2 A Example 6A

(111) Table 1 shows that the samples of Examples 1A to 7A each had a three-point bending strength of 320 MPa or higher, a tan δ of less than 10.sup.−3, an average alumina crystal grain diameter of 3 μm to 15 μm, and a water absorption of 0.2% or less. It was thus ascertained that these samples were alumina-based sintered objects which had high strength, were dense, and had low-dielectric-loss characteristics.

(112) Furthermore, as FIG. 1 shows, it is ascertained that ZrO.sub.2 crystal grains having a small diameter had come into the spaces between alumina crystal grains to inhibit the inclusion of pores.

(113) Furthermore, in each of the thin films, the number of surface voids in a region of about 200 μm×200 μm was 100 or less and the average diameter thereof was 5 μm or less. It was thus ascertained that an even film was able to be formed.

(114) In Comparative Examples 1A and 2A, the alumina-based sintered objects each had a low three-point bending strength and a tan δ exceeding 10.sup.−3 because of the too high Zr content. Furthermore, these alumina-based sintered objects had cracked.

(115) In Comparative Example 3A, the alumina-based sintered object had a low three-point bending strength and a large average Al.sub.2O.sub.3 crystal grain diameter because of the high Si content. It was found that formation of an even film on the surface of this alumina-based sintered object was difficult.

(116) In Comparative Example 4A, the alumina-based sintered object had a low three-point bending strength and a tan δ exceeding 10.sup.−3 because of the high Si and Na contents. In addition, this alumina-based sintered object had a large average Al.sub.2O.sub.3 crystal grain diameter, and it was found that formation of an even film on the surface of this alumina-based sintered object was difficult.

(117) In Comparative Example 5A, the alumina-based sintered object had a tan δ exceeding 10.sup.−3 because of the low Si content. It was found that formation of an even film on the surface of this alumina-based sintered object was difficult.

(118) In Comparative Example 6A, the alumina-based sintered object had a tan δ exceeding 10.sup.−3 because of the high Na content. This alumina-based sintered object was found to have poor dielectric loss characteristics.

Experiment 2A

(119) Next, as shown in Table 2, a ZrO.sub.2 powder and a Y.sub.2O.sub.3 powder were added to an alumina powder having a median diameter of 2 μm or less using water as a medium, and PVA was added thereto to prepare a raw-material powder. This raw-material powder was stirred and mixed for 16 hours or longer to obtain a raw-material slurry. This raw-material slurry was granulated, and the granules were packed into a molding die and molded by CIP at a molding pressure of 1.5 tons.

(120) Furthermore, the resultant molded object was subjected to a degreasing step in the air and then fired at 1,600° C. in a hydrogen atmosphere. Thus, samples of Examples 8A to 12A and Comparative Examples 7A and 8A were produced.

(121) SiO.sub.2 and Na.sub.2O were added according to need so as to give sintered objects having an Si content and an Na content within the ranges according to the present invention.

(122) As in Experiment 1A, the samples of Examples 8A to 12A and Comparative Examples 7A and 8A were evaluated for water absorption, average Al.sub.2O.sub.3 crystal grain diameter, dielectric loss tangent tan δ, and three-point bending strength. The results thereof are shown in Table 2.

(123) Furthermore, as in Experiment 1A, a surface of each of the samples (alumina-based sintered object) of Examples 8A to 12A and Comparative Examples 7A and 8A obtained above was mirror-polished so as to result in Ra<0.1 μm, and the polished surface was coated with an yttrium oxide material in a thickness of 1 μm by the aerosol deposition method. The deposition material was dried at 270° C. for 12 hours or longer as a pretreatment, and the deposition was then conducted by aerosol jetting under the same conditions as in Example 1A.

(124) The thus-obtained thin-film-coated samples of Examples 8A to 12A and Comparative Examples 7A and 8A were each examined for surface state over a range of about 200 μm×200 μm using a scanning electron microscope in the same manner as in Experiment 1A. From the image obtained, the diameters of voids and the number of the voids were determined using an image analysis software. As shown in Table 2, each sample which satisfied the number of voids of 100 or less was regarded as having been coated with an even film and indicated by “A”, and each sample which did not satisfy the requirement was regarded as having been coated with an uneven film and indicated by “B”, as in Experiment 1A.

(125) TABLE-US-00002 TABLE 2 Three- Average Al content Zr content Y content Si content Na content point crystal- State of voids in (in terms (in terms (in terms (in terms (in terms bending tanδ grain Water thin-film surface: of Al.sub.2O.sub.3) of ZrO.sub.2) of Y.sub.2O.sub.3) of SiO.sub.2) of Na.sub.2O) strength @10 to 20 diameter absorption Number of voids ≤ 100; (wt %) (wt %) (wt %) (ppm) (ppm) (MPa) MHz (μm) (%) Average diameter ≤ 5 μm Example 8A 85 10 5 300 10 350 <10.sup.−3 7 ≤0.2 A Example 9A 90 5 5 300 10 340 <10.sup.−3 5 ≤0.2 A Example 10A 65 30 5 300 10 360 <10.sup.−3 4 ≤0.2 A Example 11A 89 10 1 300 10 350 <10.sup.−3 5 ≤0.2 A Example 12A 80 10 10 300 10 320 <10.sup.−3 10 ≤0.2 A Comparative 70 10 20 300 10 290 <10.sup.−3 16 ≤0.2 A Example 7A Comparative 60 10 30 300 10 250 <10.sup.−3 18 ≤0.2 A Example 8A

(126) Table 2 shows that the samples of Examples 8A to 12A each had a three-point bending strength of 320 MPa or higher, a tan δ of less than 10.sup.−3, an average alumina crystal grain diameter of 4 μm to 10 μm, and a water absorption of 0.2% or less. It was thus ascertained that these samples were alumina-based sintered objects which had high strength, were dense, and had low-dielectric-loss characteristics.

(127) Furthermore, in each of the thin films, the number of surface voids in a region of about 200 μm×200 μm was 100 or less and the average diameter thereof was 5 μm or less. It was thus ascertained that an even film was able to be formed.

(128) In Comparative Examples 7A and 8A, the alumina-based sintered objects each had a large average Al.sub.2O.sub.3 crystal grain diameter because of the high Y content. In addition, these alumina-based sintered objects each had a low three-point bending strength.

Experiment 1B

(129) As shown in Table 3, PVA was added to an alumina powder having a purity of 99.7 wt % to 99.9 wt % and a median diameter of 2 μm or less to prepare a raw-material powder. This raw-material powder was stirred and mixed for 16 hours or longer to obtain a raw-material slurry. This raw-material slurry was granulated, and the granules were packed into a molding die and molded by CIP at a molding pressure of 1.5 tons.

(130) Furthermore, the resultant molded object was subjected to a degreasing step in the air and then fired in a hydrogen atmosphere at 1,800° C. (Examples 1B to 4B and 7B and Comparative Examples 1B to 4B), 1,700° C. (Example 5B and Comparative Example 5B), or 1,900° C. (Examples 6B and Comparative Example 6B). Thus, samples of Examples 1B to 7B and Comparative Examples 1B to 6B were produced.

(131) SiO.sub.2 and Na.sub.2O were added according to need so as to give sintered objects each having an Si content and an Na content within the ranges according to the present invention. Furthermore, the median diameter of the alumina powder was changed so that the sintered objects each had a density within the range according to the present invention.

(132) The samples of Examples 1B to 7B and Comparative Examples 1B to 6B were evaluated for density and dielectric loss tangent tan. The results thereof are shown in Table 3.

(133) In Experiment 1B and in the following Experiments 2B to 4B, the density was determined in accordance with JIS R 1634:1998. The tan δ was determined at frequencies of 10 MHz 20 MHz using an impedance analyzer. Furthermore, the average alumina crystal grain diameter was determined by mirror-polishing a cross-section of each sample, subjecting the polished cross-section to thermal etching, subsequently taking a photograph of the cross-section with a scanning electron microscope (SEM), and calculating the average crystal grain diameter by image analysis. The three-point bending strength was measured in accordance with JIS R 1601:2008. The purity of each sintered object was determined by ICP emission analysis.

(134) Furthermore, a surface of each of the samples (alumina-based sintered object) of Examples 1B to 7B and Comparative Examples 1B to 6B obtained above was mirror-polished so as to result in Ra<0.1 μm, and the polished surface was coated with an yttrium oxide material in a thickness of 1 μm by the aerosol deposition method.

(135) The deposition material was dried at 270° C. for 12 hours or longer as a pretreatment, and the deposition was then conducted by aerosol jetting under the following conditions:

(136) Sample temperature, room temperature; powder container temperature, 150° C.; raising/conveying gas, He: powder raising rate, 3 L/min; powder conveying rate, 10 L/min; powder collision angle, 60°; nozzle opening shape, 5×0.3 mm; sample-to-nozzle distance, 5 mm; sample traveling speed, 200 mm/min: number of passes for deposition, 10.

(137) The thus-obtained thin-film-coated samples of Examples 1B to 7B and Comparative Examples 1B to 6B were each examined for surface state over a range of about 200 μm×200 μm using a scanning electron microscope. From the image obtained, the diameters of voids and the number of the voids were determined using an image analysis software. As shown in Table 3, each sample which satisfied the number of voids of 100 or less was regarded as having been coated with an even film and indicated by “A”, and each sample which did not satisfy the requirement was regarded as having been coated with an uneven film and indicated by “B”. Moreover, especially preferred samples in which the average void diameter was 5 μm or less and the number of voids was less than 80 were indicated by “AA”. Consequently, “A” indicates that the number of voids was 80 to 100. The criteria for “AA”, “A” and “B” apply also in Tables 4 to 6, which will be given later.

(138) TABLE-US-00003 TABLE 3 Si content Na content Density of State of voids in Purity of (in terms (in terms sintered tanδ thin-film surface: alumina of SiO.sub.2) of Na.sub.2O) object @10 to 20 Number of voids ≤ 100; (wt %) (ppm) (ppm) (g/cm.sup.3) MHz Average diameter ≤ 5 μm Example 1B 99.9 385 4.3 3.99 <10.sup.−3 AA Example 2B 99.9 363 18.9 4.00 <10.sup.−3 AA Example 3B 99.9 492 27.0 4.00 <10.sup.−3 AA Example 4B 99.9 600 13.0 3.99 <10.sup.−3 AA Example 5B 99.9 471 6.8 3.98 <10.sup.−3 AA Example 6B 99.9 321 1.1 4.00 <10.sup.−3 AA Example 7B 99.9 203 3.4 3.99 <10.sup.−3 AA Comparative 99.9 407 41.2 3.95 >10.sup.−3 B Example 1B Comparative 99.9 54 32.4 3.99 >10.sup.−3 AA Example 2B Comparative 99.8 1305 6.3 3.94 <10.sup.−3 B Example 3B Comparative 99.8 1070 8.6 3.95 <10.sup.−3 B Example 4B Comparative 99.7 600 17.5 3.95 >10.sup.−3 B Example 5B Comparative 99.7 600 27.0 3.95 >10.sup.−3 B Example 6B

(139) Table 3 shows that the samples of Examples 1B to 7B each had a density of 3.96 g/cm.sup.3 or higher and a tan δ of less than 10.sup.−3. It was thus ascertained that these samples were alumina-based sintered objects which were dense and had low-dielectric-loss characteristics.

(140) In Comparative Example 1B, the alumina-based sintered object had a density of less than 3.96 g/cm.sup.3 because of the high Na content, and had a tan δ exceeding 10.sup.−3. This alumina-based sintered object was thus found to be poor in denseness and dielectric loss characteristics.

(141) In Comparative Example 2B, the alumina-based sintered object had a tan δ exceeding 10.sup.−3 because of the low Si content and high Na content. Namely, this alumina-based sintered object was found to have poor dielectric loss characteristics.

(142) In Comparative Example 3B, the alumina-based sintered object had a density of less than 3.96 g/cm.sup.3 because of the high Si content. Namely, this alumina-based sintered object was found to have poor denseness.

(143) In Comparative Example 4B, densification had been inhibited due to the too high Si content, and the alumina-based sintered object had a density of less than 3.96 g/cm.sup.3. Namely, this alumina-based sintered object was found to have poor denseness, making it difficult to form a dense film on the surface of the alumina-based sintered object.

(144) In Comparative Example 5B, the purity of the alumina was low and the alumina-based sintered object had a density of less than 3.96 g/cm.sup.3 and a tan δ exceeding 10.sup.3. Namely, this alumina-based sintered object was found to have poor denseness.

(145) In Comparative Example 6B, the purity of the alumina was low and the alumina-based sintered object had a density of less than 3.96 g/cm.sup.3 and a tan δ exceeding 10.sup.−3. Namely, this alumina-based sintered object was found to have poor denseness.

(146) The thin films formed on the samples of Examples 1B to 7B and Comparative Examples 2B each had a surface state in which the average diameter of voids was 5 μm or less and the number of the voids in a region of about 200 μm×200 μm was 100 or less (less than 80). It was found that an even film was able to be formed thereon.

Experiment 2B

(147) Next, as shown in Table 4, PVA was added to an alumina powder having a purity of 99.8 wt % to 99.9 wt % and a median diameter of 2 μm or less to prepare a raw-material powder. This raw-material powder was stirred and mixed for 16 hours or longer to obtain a raw-material slurry. This raw-material slurry was granulated, and the granules were packed into a molding die and molded by CIP at a molding pressure of 1.5 tons.

(148) Furthermore, the resultant molded object was subjected to a degreasing step in the air and then fired in a hydrogen atmosphere at 1,800° C. Thus, samples of Examples 9B, 118B, 13B, and 15B were produced. Meanwhile, the molded object was subjected to a degreasing step in the air and then fired in a hydrogen atmosphere at 1,900° C. Thus, samples of Examples 8B, 10B, 12B, and 14B were produced.

(149) As shown in Table 4, SiO.sub.2 and Na.sub.2O were added so as to give sintered objects each having an Si content and an Na content within the ranges according to the present invention, and MgO was added so that the ratio of the content of Mg, in terms of MgO, to the Si content, in terms of SiO.sub.2, was in the range of 0.9 to 4.1. Furthermore, the median diameter of the alumina powder was changed so that the sintered objects each had a density within the range according to the present invention.

(150) The samples of Examples 8B to 15B were evaluated for density and dielectric loss tangent tan δ. The results thereof are shown in Table 4.

(151) As Examples 8B, 9B, 12B, and 13B in Table 4 show, it was found that sintered objects having higher densities of 3.99 g/cm.sup.3 and 4.00 g/cm.sup.3 were able to be obtained.

(152) Furthermore, as in Experiment 1B, a surface of each of the samples (alumina-based sintered object) of Examples 8B to 15B was mirror-polished so as to result in Ra<0.1 μm, and the polished surface was coated with an yttrium oxide material in a thickness of 1 μm by the aerosol deposition method. The state of the surface of the thin film was examined. The results thereof are shown in Table 4.

(153) As Table 4 shows, the thin films formed on the samples of Examples 8B to 15B each had a surface state in which the average diameter of voids was 5 μm or less and the number of the voids in a region of about 200 μm×200 μm was 100 or less (less than 80). It was found that an even film was able to be formed thereon.

(154) TABLE-US-00004 TABLE 4 Si content Na content Density of State of voids in Purity of (in terms (in terms Ratio of Mg sintered tanδ thin-film surface: alumina of SiO.sub.2) of Na.sub.2O) content to object @10 to 20 Number of voids ≤ 100; (wt %) (ppm) (ppm) Si content (g/cm.sup.3) MHz Average diameter ≤ 5 μm Example 8B 99.8 600 13.0 4.0 3.99 <10.sup.−3 AA Example 9B 99.9 600 13.0 1.0 3.99 <10.sup.−3 AA Example 10B 99.9 600 13.0 0.9 3.98 <10.sup.−3 AA Example 11B 99.8 600 13.0 4.1 3.97 <10.sup.−3 AA Example 12B 99.9 170 13.0 4.0 4.00 <10.sup.−3 AA Example 13B 99.9 170 13.0 1.0 4.00 <10.sup.−3 AA Example 14B 99.9 170 13.0 0.9 3.98 <10.sup.−3 AA Example 15B 99.9 170 13.0 4.1 3.98 <10.sup.−3 AA

Experiment 3B

(155) Next, as shown in Table 5, PVA was added to an alumina powder having a purity of 99.8 wt % to 99.9 wt % and a median diameter of 2 μm or less to prepare a raw-material powder. This raw-material powder was stirred and mixed for 16 hours or longer to obtain a raw-material slurry. This raw-material slurry was granulated, and the granules were packed into a molding die and molded by CIP at a molding pressure of 1.5 tons.

(156) Furthermore, the resultant molded object was subjected to a degreasing step in the air and then fired in a hydrogen atmosphere at 1,600° C. Thus, samples of Examples 16B, 17B, 18B, and 19B were produced.

(157) The samples of Examples 16B, 17B, 18B, and 19B were evaluated for density, average Al.sub.2O.sub.3 crystal grain diameter, dielectric loss tangent tan δ, and three-point bending strength. The samples of Examples 8B, 10B, 12B, and 14B described above were also evaluated for average Al.sub.2O.sub.3 crystal grain diameter and three-point bending strength. The results thereof are shown in Table 5.

(158) The average alumina crystal grain diameter was determined by mirror-polishing a cross-section of each sample, subjecting the polished cross-section to thermal etching, subsequently taking a photograph of the cross-section with a scanning electron microscope (SEM), and calculating the average crystal grain diameter by image analysis. The three-point bending strength was measured in accordance with JIS R 1601:2008. The purity of each sintered object was determined by ICP emission analysis.

(159) As a result, it was found that sintered objects each having a density of 3.97 g/cm.sup.3 or higher and a three-point bending strength of 250 MPa or higher were obtained as shown by Examples 8B and 16B and Examples 12B and 18B in Table 5.

(160) Furthermore, as in Experiment 1B, a surface of each of the samples (alumina-based sintered object) of Examples 16B to 19B was mirror-polished so as to result in Ra<0.1 μm, and the polished surface was coated with an yttrium oxide material in a thickness of 1 μm by the aerosol deposition method. The state of the surface of the thin film was examined. The results thereof are shown in Table 5.

(161) As Table 5 shows, the thin films formed on the samples of Examples 16B and 18B each had a surface state in which the average diameter of voids was 5 μm or less and the number of the voids in a region of about 200 μm×200 μm was 100 or less (less than 80). It was found that an even film was able to be formed thereon. Meanwhile, the thin films formed on the samples of Examples 17B and 19B each had a surface state in which the average diameter of voids was 5 μm or less and the number of the voids in a region of about 200 μm×200 μm was 80 to 100. It was found that an even film was able to be formed thereon.

(162) TABLE-US-00005 TABLE 5 Average Three- Si content Na content crystal Density of point State of voids in (in terms (in terms grain sintered tanδ bending thin-film surface: of SiO.sub.2) of Na.sub.2O) diameter object @10 to 20 strength Number of voids ≤ 100; (ppm) (ppm) (μm) (g/cm.sup.3) MHz (MPa) Average diameter ≤ 5 μm Example 16B 600 13.0 3.0 3.97 <10.sup.−3 300 AA Example 8B 600 13.0 40.0 3.99 <10.sup.−3 270 AA Example 17B 600 13.0 2.0 3.96 <10.sup.−3 310 A Example 10B 600 13.0 45.0 3.98 <10.sup.−3 240 AA Example 18B 170 13.0 3.0 3.97 <10.sup.−3 315 AA Example 12B 170 13.0 40.0 4.00 <10.sup.−3 270 AA Example 19B 170 13.0 2.0 3.96 <10.sup.−3 320 A Example 14B 170 13.0 45.0 3.98 <10.sup.−3 245 AA

Experiment 4B

(163) Next, PVA was added to an alumina powder having the same alumina purity and median diameter as in Example 18B to prepare a raw-material powder. This raw-material powder was stirred and mixed for 16 hours or longer to obtain a raw-material slurry. This raw-material slurry was granulated, and the granules were packed into a molding die and molded by CIP at a molding pressure of 1.5 tons.

(164) Furthermore, the resultant molded object was subjected to a degreasing step in the air and then fired under the conditions shown in Table 6. Thus, samples of Examples 20B to 22B and Comparative Examples 7B to 10B were produced.

(165) The samples of Examples 20B to 22B and Comparative Examples 7B to 10B were evaluated for density and dielectric loss tangent tan. The results thereof are shown in Table 6 together with the results obtained in Example 18B.

(166) Furthermore, as in Experiment 1B, a surface of each of the samples (alumina-based sintered object) of Examples 20B to 22B and Comparative Examples 7B to 10B was mirror-polished so as to result in Ra<0.1 μm, and the polished surface was coated with an yttrium oxide material in a thickness of 1 μm by the aerosol deposition method. The state of the surface of the thin film was examined. The results thereof are shown in Table 6 together with the results obtained in Example 18B.

(167) TABLE-US-00006 TABLE 6 State of voids in thin-film surface: Number Density of voids of ≤100; Firing sintered tanδ Average Firing temperature object @10 to diameter atmosphere (° C.) (g/cm.sup.3) 20 MHz ≤5 μm Example 18B hydrogen 1600 3.97 <10.sup.−3 AA Example 20B hydrogen 1700 3.98 <10.sup.−3 AA Example 21B hydrogen 1800 3.99 <10.sup.−3 AA Example 22B hydrogen 1900 4.00 <10.sup.−3 AA Comparative hydrogen 1500 3.81 <10.sup.−3 B Example 7B  Comparative hydrogen 2000 4.00 >10.sup.−3 AA Example 8B  Comparative air 1600 3.91 >10.sup.−3 B Example 9B  Comparative air 1800 3.95 >10.sup.−3 B Example 10B

(168) It was found from Examples 18B and 20B to 22B that the sintered objects obtained through firing in a hydrogen atmosphere at 1,600° C. to 1.900° C. each had a density of 3.96 g/cm.sup.3 or higher and a dielectric loss tangent tan δ of less than 10.sup.−3.

(169) Furthermore, as Table 6 shows, the thin films formed on the samples of Examples 18B and 20B to 22B each had a surface state in which the average diameter of voids was 5 μm or less and the number of the voids in a region of about 200 μm×200 μm was 100 or less (less than 80). It was found that an even film was able to be formed thereon.

(170) This application is based on a Japanese patent application filed on Oct. 5, 2017 (Application No. 2017-195292), a Japanese patent application filed on Sep. 25, 2018 (Application No. 2018-178652), and a Japanese patent application filed on Sep. 26, 2018 (Application No. 2018-180299), the contents thereof being incorporated herein by reference.

INDUSTRIAL APPLICABILITY

(171) The present invention is usable as constituent members for use in, for example, production devices in the field of semiconductor production and the field of liquid-crystal display device production. For example, the present invention is suitable for use as members for use in plasma treatment devices, etchers for semiconductor/liquid-crystal display device production, CVD devices, etc. The alumina-based sintered objects according to the present invention may be used as such, or may be used as plasma-resistant members after a plasma-resistant corrosion-resistant film or corrosion-resistant layer is formed on a part or all of the surfaces of the alumina-based sintered objects as substrates.

REFERENCE SIGNS LIST

(172) 1 Al.sub.2O.sub.3 crystal grain 2 ZrO.sub.2 crystal grain 3 Pore