JPH0443867B2 - - Google Patents
Info
- Publication number
- JPH0443867B2 JPH0443867B2 JP6903290A JP6903290A JPH0443867B2 JP H0443867 B2 JPH0443867 B2 JP H0443867B2 JP 6903290 A JP6903290 A JP 6903290A JP 6903290 A JP6903290 A JP 6903290A JP H0443867 B2 JPH0443867 B2 JP H0443867B2
- Authority
- JP
- Japan
- Prior art keywords
- porcelain
- particle size
- plastic raw
- wet
- raw materials
- 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.)
- Expired
Links
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 68
- 229910052573 porcelain Inorganic materials 0.000 claims description 36
- 239000002994 raw material Substances 0.000 claims description 30
- 239000002245 particle Substances 0.000 claims description 23
- 239000004575 stone Substances 0.000 claims description 15
- 239000000377 silicon dioxide Substances 0.000 claims description 14
- 239000004927 clay Substances 0.000 claims description 13
- 229910052906 cristobalite Inorganic materials 0.000 claims description 11
- 239000004576 sand Substances 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 9
- 239000010433 feldspar Substances 0.000 claims description 8
- 238000004519 manufacturing process Methods 0.000 claims description 7
- 238000001556 precipitation Methods 0.000 claims description 2
- 238000000926 separation method Methods 0.000 claims 1
- 238000001238 wet grinding Methods 0.000 claims 1
- 239000010453 quartz Substances 0.000 description 18
- 238000010298 pulverizing process Methods 0.000 description 12
- 239000000463 material Substances 0.000 description 8
- 230000000052 comparative effect Effects 0.000 description 7
- 238000005245 sintering Methods 0.000 description 5
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 3
- 238000005452 bending Methods 0.000 description 3
- 239000013078 crystal Substances 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 238000007796 conventional method Methods 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 235000019589 hardness Nutrition 0.000 description 2
- 239000002075 main ingredient Substances 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 239000011802 pulverized particle Substances 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 229910004298 SiO 2 Inorganic materials 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012212 insulator Substances 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 238000004445 quantitative analysis Methods 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
Description
(産業上の利用分野)
本発明は、食器用磁器や電気用磁器として用途
が広く、かつ機械的強度の大きい磁器製品を生成
するクリストバライト磁器素地の製造方法に関す
るものである。
(従来の技術)
磁器は白色度および機械的強度に優れているた
め、食器や置物、碍子のような電気用製品などに
広く用いられているが、これらの磁器の製造方法
の1つとして従来より、石英および絹雲母(セリ
サイト)を主成分とする天草陶石や泉山陶石な
ど、即ち石英成分の多い陶石を主原料とし、珪
砂、長石、粘土等を加えて粉砕、混合などの原材
料処理工程を行つた後成型工程および乾燥、焼成
工程を経て石英成分をクリストバライトへ転移さ
せ、磁器固有の機械的強度を発現しようとする方
法がある。とくに陶石原料として良質高品位の天
草陶石を用いるとその中に含まれる石英が微細で
あるので、焼成後の磁器中にクリストバライト結
晶が生成し機械的強度に優れた高品質の磁器を提
供することができる。
ところが近年、良質で高品位の天草陶石が枯渇
化する傾向にあり、その代替原料として石英成分
である珪砂(平均粒径700μm程度)を用い、長
石、陶石、粘土などとともに湿式粉砕して磁器素
地を製造することが提案されている。
(発明が解決しようとする課題)
しかしながら、平均粒径700μm程度の原珪砂、
長石、珪石等の比較的硬度の硬い非可塑性原料と
陶石、粘土などの硬度の低い可塑性原料とを同時
に湿式粉砕すると非可塑性原料である硬質の珪砂
や長石は粉砕されにくいので、調合原料全体の粉
砕効率が悪くなつて均質粉砕ができず、粉砕原料
素地中に粗粒の石英(粒径30μm程度以上)が残
留する。焼成過程で微細な石英は溶融し、かつそ
の融液からクリストバライトが晶出するが石英が
粗粒であると焼結後も粗粒石英のまま磁器中に存
在し、磁器そのものが不均質となり、これにより
磁器の機械的強度が低下する。その上、素地中に
残留した石英は磁器の透明度をも減じるため、こ
の点においても磁器製品としての品質低下を招く
という欠点を有していた。
(課題を解決するための手段)
そこで、本発明は上記の点に鑑み、硬度や性状
の異なる各種原料を同時粉砕することによつて生
ずる粉砕の不均質を解消し、粗粒の石英の残留を
抑制し、石英のクリストバライトへの転移を促進
して機械的強度の強いクリストバライト磁器を得
ることを目的としてなされたクリストバライト磁
器素地の製造方法であり、珪砂、長石等の非可塑
性原料に沈澱分離を防止する量の粘土を加えて所
定粒度に湿式粉砕し、その後両粉砕物に残余の粘
土質を加えて混合し、組成および粒度を調製する
ことを特徴とするものである。
特に本発明は、従来性状の異なる各種原料を同
時粉砕することにより生じていた粉砕の不均質
を、性状及び硬度により区分して、非可塑性原料
および可塑性原料をそれぞれ区分して所定粒度に
湿式粉砕するものである。そしてさらに、非可塑
性原料である珪砂、珪石、長石等は粉砕後におい
て沈澱分離するので、粉砕物の沈澱分離を防止す
るため、粘土を沈澱分離を防止する量、通常は粉
砕物の4〜8重量%、好ましくは5〜6重量%添
加することが大切である。また組成および素地の
粒度は残余粘土分の混合後に所定の組成および粒
度となるように非可塑性原料および可塑性原料の
混合および粒度を予め算出し、それに一致させる
ことも大切である。なお、微細なアルミナ粉末を
アルミナ源原料として用いるときは、可塑性原料
の粉砕時に加えて凝集を解粒する程度でもよい。
(実施例)
まず、珪砂と長石などの非可塑性原料を予め決
められた所定の割合で混合し、さらに沈澱防止を
目的として5%前後の粘土を加えてボールミルに
て粒径が10μm以上の粒度の粗粒部が第1表の素
地粒度に記載する21〜31wt%、平均粒径が3
〜6μmとなるまで湿式粉砕する。一方、陶石など
の可塑性原料と所望の場合に微細なアルミナ粉末
等も所定量加え、ボールミルにて第1表の素地粒
度に記載する粒径10μm以上の粒度の粗粒部が
17〜42wt%、平均粒径が3〜7μmとなるまで湿
式粉砕する。次に、先の別々に湿式粉砕された非
可塑性原料と可塑性原料とを第1表の素地粒度
に記載する27wt%となるように混合、さらに残
余の粘土を加えて素地組成が第1表記載の素地組
成および素地粒度となるように調合し、本発明
のNo.1〜No.6のクリストバライト磁器素地を製造
した。
これに対し、1番目の比較例として磁器素地A
を珪砂を加えず陶石、珪石、長石などを予め決め
られた割合で混合し、組成および粒度が上記本発
明とほぼ同じになるように同時に湿式粉砕し、続
いて先の実施例と同様、粘土とタンク混合するこ
とで第1表比較例Aに示す磁器素地を製造した。
又、2番目の比較例として磁器素地Bを珪砂、陶
石、長石、粘土などを同時に湿式粉砕混合するこ
とにより第1表比較例Bに示す磁器素地を製造し
た。
(作用及び効果)
上記のとおり、本発明の方法により製造された
磁器素地、及び比較例として製造した磁器素地と
を常法により成型、乾燥後焼成を昇温速度10〜20
℃/hr、焼結温度1200〜1220℃、焼結温度での保
持時間0.5〜2hr、降温速度10〜20℃/hrで行い、
得られた磁器の性状(熱膨脹率、析出結晶量、抗
折強度、残留石英粒径)を素地の製造条件ととも
に第1表に示した。
なお、第1表において磁器の析出結晶量はX線
回折定量法により測定、また、抗折強度は12φ×
100mmの円柱状供試体を3点支持曲げ試験法によ
り測定、さらに磁器中の残留石英粒径は走査型電
子顕微鏡により測定した値である。
(Field of Industrial Application) The present invention relates to a method for producing a cristobalite porcelain base, which produces a porcelain product that has a wide range of uses as tableware porcelain and electrical porcelain, and has high mechanical strength. (Prior art) Porcelain has excellent whiteness and mechanical strength, so it is widely used in tableware, ornaments, and electrical products such as insulators. The main ingredients are Amakusa pottery stone and Izumiyama pottery stone, which have quartz and sericite as their main ingredients. There is a method in which the quartz component is transferred to cristobalite through a raw material processing step, followed by a molding step, drying, and firing step, thereby developing the mechanical strength unique to porcelain. In particular, when high-quality Amakusa pottery stone is used as a raw material for pottery stone, the quartz contained therein is fine, so cristobalite crystals are formed in the porcelain after firing, providing high-quality porcelain with excellent mechanical strength. can do. However, in recent years, high-quality Amakusa pottery stone has become depleted, and as an alternative raw material, silica sand (average particle size of about 700 μm), which is a quartz component, is used and wet-pulverized along with feldspar, pottery stone, clay, etc. It is proposed to produce porcelain blanks. (Problem to be solved by the invention) However, raw silica sand with an average particle size of about 700 μm,
If relatively hard non-plastic raw materials such as feldspar and silica stone are simultaneously wet-pulverized with low-hardness plastic raw materials such as pottery stone and clay, the hard silica sand and feldspar, which are non-plastic raw materials, are difficult to crush, so the entire blended raw material is The pulverization efficiency deteriorates, making it impossible to achieve homogeneous pulverization, and coarse quartz particles (particle size of about 30 μm or more) remain in the pulverized raw material matrix. During the firing process, fine quartz melts and cristobalite crystallizes from the melt, but if the quartz is coarse-grained, the coarse-grained quartz remains in the porcelain even after sintering, and the porcelain itself becomes heterogeneous. This reduces the mechanical strength of the porcelain. Furthermore, since the quartz remaining in the base material also reduces the transparency of the porcelain, this also has the disadvantage of causing a deterioration in the quality of the porcelain product. (Means for Solving the Problems) Therefore, in view of the above points, the present invention eliminates the non-uniformity of pulverization caused by simultaneously pulverizing various raw materials with different hardnesses and properties, and eliminates the non-uniformity of pulverization that occurs when coarse quartz remains. This is a method for producing cristobalite porcelain with the aim of suppressing the silica sand, promoting the transition of quartz to cristobalite, and obtaining cristobalite porcelain with strong mechanical strength. It is characterized by adding a certain amount of clay and wet-pulverizing it to a predetermined particle size, and then adding and mixing the remaining clay to both crushed products to adjust the composition and particle size. In particular, the present invention solves the non-uniformity of pulverization that conventionally occurred by simultaneously pulverizing various raw materials with different properties, by classifying them according to their properties and hardness, and separating non-plastic raw materials and plastic raw materials into wet pulverization to a predetermined particle size. It is something to do. Furthermore, since silica sand, silica stone, feldspar, etc., which are non-plastic raw materials, are precipitated and separated after being crushed, in order to prevent the sedimentation of the pulverized material, clay is added in an amount that prevents the pulverized material from settling, usually 4 to 8 ml of clay. It is important to add 5% to 6% by weight, preferably 5 to 6% by weight. It is also important to calculate the composition and particle size of the base material in advance so that the mixture of the non-plastic raw materials and the plastic raw materials and the particle size match the predetermined composition and particle size after mixing the residual clay. Note that when fine alumina powder is used as an alumina source material, it may be added at the time of pulverizing the plastic raw material to disintegrate agglomerates. (Example) First, silica sand and non-plastic raw materials such as feldspar are mixed in a predetermined ratio, and approximately 5% clay is added to prevent precipitation, and the mixture is milled in a ball mill to obtain particles with a particle size of 10 μm or more. The coarse grain part of
Wet grind until ~6 μm. On the other hand, a predetermined amount of plastic raw materials such as pottery stone and fine alumina powder, etc., are added if desired, and a coarse grain portion with a grain size of 10 μm or more as described in the base grain size in Table 1 is produced using a ball mill.
Wet grind until the powder has a content of 17 to 42 wt% and an average particle size of 3 to 7 μm. Next, the separately wet-milled non-plastic raw material and plastic raw material are mixed to give the base particle size of 27wt% as shown in Table 1, and the remaining clay is added to make the base composition as shown in Table 1. The cristobalite porcelain bases No. 1 to No. 6 of the present invention were manufactured by preparing the base composition and the base particle size as follows. On the other hand, as the first comparative example, porcelain base A
was mixed with pottery stone, silica stone, feldspar, etc. in a predetermined ratio without adding silica sand, and wet-pulverized at the same time so that the composition and particle size were almost the same as those of the present invention, and then, as in the previous example, A porcelain base shown in Comparative Example A in Table 1 was produced by mixing with clay in a tank.
In addition, as a second comparative example, a porcelain base shown in Comparative Example B in Table 1 was produced by wet-pulverizing porcelain base B with silica sand, pottery stone, feldspar, clay, etc. at the same time. (Functions and Effects) As described above, the porcelain base produced by the method of the present invention and the porcelain base produced as a comparative example were molded by a conventional method, and fired after drying at a temperature increase rate of 10 to 20.
℃/hr, sintering temperature 1200-1220℃, holding time at sintering temperature 0.5-2hr, cooling rate 10-20℃/hr,
The properties of the obtained porcelain (thermal expansion coefficient, amount of precipitated crystals, bending strength, residual quartz grain size) are shown in Table 1 together with the manufacturing conditions of the base material. In addition, in Table 1, the amount of precipitated crystals of porcelain is measured by X-ray diffraction quantitative method, and the bending strength is 12φ×
A 100 mm cylindrical specimen was measured using a three-point support bending test method, and the residual quartz grain size in the porcelain was measured using a scanning electron microscope.
【表】【table】
【表】
この表に示すように、非可塑性原料と可塑性原
料とを別々に所望粒度まで湿式粉砕する本発明の
製造方法により製造された素地を焼結して得られ
た磁器は、非可塑性原料と可塑性原料とを同時に
湿式粉砕して製造された素地Bを焼結して得られ
た磁器(比較例B)に比べて抗折強度が大きく、
かつ磁器中に残る石英粒径も小さいので強度に優
れている。
また、珪砂を用いず製造される素地Aから得ら
れた磁器(比較例A)に比べても強度、残留石英
粒径ともに劣ることなく、枯渇化傾向にある良質
の陶石のSiO2成分を一部珪砂に代替させても磁
器の品質を維持することができる。ただ、本発明
においても可塑性原料、非可塑性原料とも粉砕粒
度が粗くなると残留石英粒径が大きくなり機械的
強度が低下するので、非可塑性原料の粉砕粒度は
10μm以上が30%以下、可塑性原料の粉砕粒度は
10μm以上が37%以上であることが好ましい。
以上の説明からも明らかなように、本発明は磁
器中の粗粒石英の残留を抑制し、石英のクリスト
バライトへの転移を促進して、強度に優れた高品
質の磁器を提供することのできる磁器素地の製造
方法として、従来の問題点を一掃し、産業の発展
に寄与するところは極めて大きいものである。[Table] As shown in this table, the porcelain obtained by sintering the base material manufactured by the manufacturing method of the present invention, in which non-plastic raw materials and plastic raw materials are separately wet-pulverized to the desired particle size, is made from non-plastic raw materials. The flexural strength is greater than that of the porcelain obtained by sintering the base material B produced by wet-pulverizing and the plastic raw material at the same time (Comparative Example B).
Moreover, the quartz grains remaining in the porcelain are small in size, so it has excellent strength. In addition, the strength and residual quartz grain size are not inferior to the porcelain obtained from base A manufactured without using silica sand (comparative example A), and the SiO 2 component of high-quality pottery stone, which is tending to be depleted, is The quality of porcelain can be maintained even if some of it is replaced with silica sand. However, even in the present invention, when the pulverized particle size of both plastic and non-plastic raw materials becomes coarse, the residual quartz particle size increases and the mechanical strength decreases, so the pulverized particle size of the non-plastic raw material is
10μm or more is 30% or less, and the crushed particle size of plastic raw materials is
It is preferable that 37% or more is 10 μm or more. As is clear from the above description, the present invention can suppress the residual coarse-grained quartz in porcelain, promote the transition of quartz to cristobalite, and provide high-quality porcelain with excellent strength. As a manufacturing method for porcelain bases, it eliminates the problems of the conventional method and greatly contributes to the development of industry.
Claims (1)
止する量の粘土を加えて所定粒度に湿式粉砕し、
これとは別に陶石等の可塑性原料を所定粒度に湿
式粉砕し、その後両粉砕物に残余の粘土質を加え
て混合することを特徴とするクリストバライト磁
器素地の製造方法。 2 可塑性原料の湿式粉砕後の平均粒度を素地の
平均粒度と同等もしくはそれより小さくする請求
項1記載のクリストバライト磁器素地の製造方
法。[Scope of Claims] 1. Clay is added in an amount that prevents precipitation and separation to non-plastic raw materials such as silica sand and feldspar, and the mixture is wet-pulverized to a predetermined particle size.
Separately, a method for producing a cristobalite porcelain base is characterized in that a plastic raw material such as pottery stone is wet-pulverized to a predetermined particle size, and then residual clay is added to and mixed with both crushed products. 2. The method for producing a cristobalite porcelain base according to claim 1, wherein the average particle size of the plastic raw material after wet milling is equal to or smaller than the average particle size of the base.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6903290A JPH03271148A (en) | 1990-03-19 | 1990-03-19 | Production of cristobalite ceramic body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP6903290A JPH03271148A (en) | 1990-03-19 | 1990-03-19 | Production of cristobalite ceramic body |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPH03271148A JPH03271148A (en) | 1991-12-03 |
| JPH0443867B2 true JPH0443867B2 (en) | 1992-07-17 |
Family
ID=13390834
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP6903290A Granted JPH03271148A (en) | 1990-03-19 | 1990-03-19 | Production of cristobalite ceramic body |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03271148A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5374350B2 (en) * | 2009-12-14 | 2013-12-25 | 株式会社ノリタケカンパニーリミテド | White porcelain manufacturing method and glaze suitable therefor |
-
1990
- 1990-03-19 JP JP6903290A patent/JPH03271148A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPH03271148A (en) | 1991-12-03 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPS61168560A (en) | High strength feldspar ceramic and manufacture | |
| JPH09502689A (en) | White porcelain ceramic composition | |
| US5641720A (en) | Corundum porcelain composition, processes for its preparation and use | |
| GB1592267A (en) | Production of electrofusion corundum | |
| US2768087A (en) | Silicon carbide aggregates | |
| JPH0443867B2 (en) | ||
| JPH05345662A (en) | Production of forsterite ceramic | |
| JPH0611668B2 (en) | Manufacturing method of high strength porcelain products | |
| JP3083681B2 (en) | MgO-SiO2-based porcelain and method of manufacturing the same | |
| JPH0443866B2 (en) | ||
| CN115872723A (en) | Earthenware green body material | |
| JPH0544428B2 (en) | ||
| RU2366637C1 (en) | Method for preparation of high-density water slip based on lithium-alumosilicate glass | |
| JP2000169201A (en) | Production of admixture for cement and composition using the admixture | |
| KR20190056494A (en) | Method for fabricating the Punchong porcelain used Muan Clay and Punchong porcelain produced by the method | |
| KR102820775B1 (en) | Yttria sintered body and manufacturing method of the same | |
| JPH06305809A (en) | High-strength ceramic whiteware and its production | |
| JPS58156569A (en) | Manufacture of pottery clay | |
| JPH0624728A (en) | Production of cristobalite | |
| JPH0420586A (en) | Manufacture of sintered alumina abrasive grain | |
| JPH02275753A (en) | High strength feldspathic porcelain | |
| JPH0139987B2 (en) | ||
| JPH04300235A (en) | Production of ceramic body | |
| Andreeva et al. | Technological implications in increasing the strength of porcelain | |
| JPS5935064A (en) | Chamotte and manufacture |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| LAPS | Cancellation because of no payment of annual fees |