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JPH0443866B2 - - Google Patents
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JPH0443866B2 - - Google Patents

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Publication number
JPH0443866B2
JPH0443866B2 JP6903190A JP6903190A JPH0443866B2 JP H0443866 B2 JPH0443866 B2 JP H0443866B2 JP 6903190 A JP6903190 A JP 6903190A JP 6903190 A JP6903190 A JP 6903190A JP H0443866 B2 JPH0443866 B2 JP H0443866B2
Authority
JP
Japan
Prior art keywords
porcelain
silica sand
quartz
particle size
base
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
Application number
JP6903190A
Other languages
Japanese (ja)
Other versions
JPH03271147A (en
Inventor
Kazuo Yamaguchi
Satoru Tanaka
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.)
NGK Insulators Ltd
Original Assignee
NGK Insulators Ltd
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 NGK Insulators Ltd filed Critical NGK Insulators Ltd
Priority to JP6903190A priority Critical patent/JPH03271147A/en
Publication of JPH03271147A publication Critical patent/JPH03271147A/en
Publication of JPH0443866B2 publication Critical patent/JPH0443866B2/ja
Granted legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

(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、できあがつた磁器製品の気孔率が小さくなり
緻密で機械的強度に優れ、かつ色調の明るい高品
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、
長石等の比較的硬度の硬い非可塑性原料と陶石、
粘土等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する
ことになり、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ことになる。
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、枯渇化が著
しい良質の陶石の代替原料として珪砂を用い、し
かも粉砕工程での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、最
大粒径が100μm以下でかつ平均粒径が5〜35μm
に分級された珪砂を、磁器素地構成の前記珪砂以
外の可塑性原料および非可塑性原料とともに湿式
粉砕した後、粘土質を加えて混合することを特徴
とするものである。 本発明は特にクリストバライト磁器において従
来一般的に用いられている陶石の原料枯渇にとも
ない石英分を、多量に産出する珪砂の特定粒度に
分級された分級珪砂で補おうとするもので、最大
粒径が100μm以下でかつ平均粒径が5〜35μmに
分級された珪砂を用いることが最も重要である。
そして最大粒径を100μm以下とするのは100μm以
上の粗い珪砂が存在すると後工程の粉砕工程にお
いても細かく粉砕されず、30〜40μmの石英粒と
して磁器中に残留し、機械的強度の低下をきたす
ので好ましくない。また平均粒径を5〜35μmと
限定するのは5μm未満であると溶融する石英分が
多くなつてクリストバライト磁器特有の高強度が
得られなくなり、反対に35μmを超えると磁器の
焼結性が低下し、密度低下が著しくなつて機械的
強度が低下する。従つて、分級珪砂の最大粒径と
平均粒径は極めて重要である。 (実施例) まず、珪砂を乾式粉砕して最大粒径および平均
粒径が第1表記載の粒度となるように粒度調整を
行つた分級珪砂と、陶石、長石、その他の原料と
を所望の素地組成となるように原石を調合し、ボ
ールミルにて粒径10μm以上の粒度の粗粒部が第
1表素地粒度に記載する25〜29wt%となるま
で湿式粉砕を行つて原石スラリーとした。続い
て、この原石スラリーに粘土を加えてタンク混合
することにより第1表に記載する素地組成及び素
地粒度に調整し、No.5〜No.11の本発明のクリス
トバライト磁器素地を製造した。 これに対し、従来例として磁器素地Aを分級珪
砂を全く用いず陶石、長石、粘土及びその他の原
料を第1表に記載する素地組成となるように調合
すること以外は先の実施例と同じ条件で製造し、
又、2番目の従来例として磁器素地Bを先の実施
例の分級珪砂に代えて分級していない原珪砂(平
均粒径700μm程度)を用いること以外は先の実施
例と同じ条件で製造した。 また、本発明の珪砂の最大粒径および平均粒径
が本発明の数値限定範囲外であるものを比較例と
して上記と同様に調整し、粒径の粗い比較例No.1
〜No.4および粒径の細かい比較例No.12〜No.15をそ
れぞれ準備した。 (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お
よび実施例として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
1200〜1250℃、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 the porosity of the finished porcelain product is reduced, making it dense, excellent in mechanical strength, and bright in color. We can provide quality porcelain. 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,
Relatively hard non-plastic raw materials such as feldspar and pottery stone,
When wet-pulverizing low-hardness plastic raw materials such as clay at the same time, hard silica sand and feldspar, which are non-plastic raw materials, are difficult to crush, so the crushing efficiency of the entire blended raw material becomes poor, and homogeneous crushing is not possible, resulting in the formation of particles in the crushed raw material base. Coarse-grained quartz (grain size of approximately 30 μm or more) remains.
During the firing process, fine quartz melts and cristobalite crystallizes from the melt, but if the quartz is coarse-grained, it will remain in the porcelain as coarse-grained quartz even after sintering, and the porcelain itself will become This results in non-uniformity, which 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 uses silica sand as a substitute raw material for high-quality pottery stone, which is being rapidly depleted, and also suppresses the residue of coarse quartz during the crushing process. , is a method for producing cristobalite porcelain with the aim of promoting the transition of quartz to cristobalite to obtain porcelain with strong mechanical strength.
The method is characterized in that silica sand classified into 1 is wet-pulverized together with plastic raw materials and non-plastic raw materials other than the silica sand of the porcelain base composition, and then clay is added and mixed. The present invention aims to compensate for the quartz content caused by the depletion of the raw material of pottery stone, which has traditionally been commonly used in cristobalite porcelain, with classified silica sand that has been classified to a specific grain size of silica sand that is produced in large quantities. It is most important to use silica sand classified to have a grain size of 100 μm or less and an average particle size of 5 to 35 μm.
The reason for setting the maximum particle size to 100 μm or less is that if coarse silica sand of 100 μm or more is present, it will not be finely crushed in the subsequent crushing process and will remain in the porcelain as quartz grains of 30 to 40 μm, resulting in a decrease in mechanical strength. This is not desirable as it may cause damage. In addition, the average grain size is limited to 5 to 35 μm. If it is less than 5 μm, a large amount of quartz will melt, making it impossible to obtain the high strength characteristic of cristobalite porcelain. On the other hand, if it exceeds 35 μm, the sinterability of the porcelain will decrease. However, the density decreases significantly and the mechanical strength decreases. Therefore, the maximum particle size and average particle size of classified silica sand are extremely important. (Example) First, the desired classified silica sand, which is obtained by dry-pulverizing silica sand and adjusting the particle size so that the maximum particle size and average particle size become the particle sizes listed in Table 1, and chinastone, feldspar, and other raw materials are used. The raw stone was mixed to have a base composition of , and wet-pulverized using a ball mill until the coarse particles with a particle size of 10 μm or more reached 25 to 29 wt% as described in Table 1: Base Particle Size to obtain a raw stone slurry. . Subsequently, clay was added to this raw stone slurry and mixed in a tank to adjust the base composition and base particle size as shown in Table 1, thereby producing cristobalite porcelain bases No. 5 to No. 11 of the present invention. On the other hand, as a conventional example, porcelain base A is the same as the previous example except that no classified silica sand is used at all, and pottery stone, feldspar, clay, and other raw materials are mixed to have the base composition shown in Table 1. Manufactured under the same conditions,
In addition, as a second conventional example, porcelain base B was manufactured under the same conditions as the previous example except that unclassified raw silica sand (average particle size of about 700 μm) was used instead of the classified silica sand of the previous example. . In addition, the silica sand of the present invention whose maximum particle size and average particle size are outside the numerical limit range of the present invention was prepared as a comparative example in the same manner as above, and Comparative Example No. 1 with a coarse particle size was prepared.
- No. 4 and Comparative Examples No. 12 to No. 15 with fine particle sizes were prepared, respectively. (Actions and Effects) As described above, the porcelain base produced by the method of the present invention, the porcelain base produced as a comparative example, and the porcelain base as an example were molded by a conventional method,
After drying, sintering at a heating rate of 10 to 20℃/hr, sintering temperature
1200~1250℃, holding time at sintering temperature 0.5~2hr,
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、SiO2成分として特定粒
径に分級された分級珪砂を用いる本発明の製造方
法により製造された素地を焼結して得られた磁器
は、SiO2成分として分級されていない原珪砂を
用いて製造された素地Bを焼結して得られた磁器
(従来例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、透明度と
もに優れている。 また、珪砂を用いず製造される素地Aから得ら
れた磁器(従来例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。 また、本発明品は比較例に比べ磁器中に残留す
る石英粒径あるいは磁器中に析出するクリストバ
ライト結晶量において異なり、結果的に機械的強
度に優れていることが確認された。 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、強度及び透明度と
も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 using classified silica sand classified to a specific particle size as the SiO 2 component is Compared to porcelain obtained by sintering base material B manufactured using unclassified raw silica sand (conventional example B), the bending strength is greater, and the quartz grain size remaining in the porcelain is also smaller, resulting in stronger strength. Excellent transparency. In addition, the strength and residual quartz grain size are not inferior to porcelain obtained from base A manufactured without using silica sand (conventional example A), and the SiO 2 component of high-quality pottery stone, which is on the decline, can be used. The quality of porcelain can be maintained even if some of it is replaced with silica sand. Furthermore, it was confirmed that the products of the present invention were different from the comparative examples in terms of the quartz grain size remaining in the porcelain or the amount of cristobalite crystals precipitated in the porcelain, and as a result, they were superior in mechanical strength. As is clear from the above description, the present invention suppresses the residual coarse quartz in porcelain, promotes the transition of quartz to cristobalite, and provides high quality porcelain with excellent strength and transparency. As a method for manufacturing porcelain bases that can be used in a variety of ways, it eliminates the problems of the past and greatly contributes to the development of industry.

Claims (1)

【特許請求の範囲】[Claims] 1 最大粒径が100μm以下でかつ平均粒径が5〜
35μmに分級された珪砂を、磁器素地構成の前記
珪砂以外の可塑性原料および非可塑性原料ととも
に湿式粉砕した後、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。
1 The maximum particle size is 100μm or less and the average particle size is 5~
A method for producing a cristobalite porcelain base, characterized in that silica sand classified to 35 μm is wet-pulverized together with plastic raw materials and non-plastic raw materials other than the silica sand in the porcelain base composition, and then clay is added and mixed.
JP6903190A 1990-03-19 1990-03-19 Production of cristobalite ceramic body Granted JPH03271147A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6903190A JPH03271147A (en) 1990-03-19 1990-03-19 Production of cristobalite ceramic body

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6903190A JPH03271147A (en) 1990-03-19 1990-03-19 Production of cristobalite ceramic body

Publications (2)

Publication Number Publication Date
JPH03271147A JPH03271147A (en) 1991-12-03
JPH0443866B2 true JPH0443866B2 (en) 1992-07-17

Family

ID=13390808

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6903190A Granted JPH03271147A (en) 1990-03-19 1990-03-19 Production of cristobalite ceramic body

Country Status (1)

Country Link
JP (1) JPH03271147A (en)

Also Published As

Publication number Publication date
JPH03271147A (en) 1991-12-03

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