JPS6020342B2 - Low thermal expansion porcelain composition - Google Patents
Low thermal expansion porcelain compositionInfo
- Publication number
- JPS6020342B2 JPS6020342B2 JP51120902A JP12090276A JPS6020342B2 JP S6020342 B2 JPS6020342 B2 JP S6020342B2 JP 51120902 A JP51120902 A JP 51120902A JP 12090276 A JP12090276 A JP 12090276A JP S6020342 B2 JPS6020342 B2 JP S6020342B2
- Authority
- JP
- Japan
- Prior art keywords
- thermal expansion
- low thermal
- temperature range
- firing temperature
- porcelain composition
- 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
Landscapes
- Compositions Of Oxide Ceramics (AREA)
Description
【発明の詳細な説明】
本発明は機械的強度、耐蝕性、可塑成型性の点で通常の
磁器に遜色なく耐熱性の面で優れた特性を示すべタラィ
ト等の含リチウム物質と粘土質原料とよりなる低熱膨脹
性磁器組成物の改良に関するもので、特にその焼成温度
範囲が広くなるようにして工業的に有利な低熱膨脹性磁
器を得るようにしたものである。Detailed Description of the Invention The present invention uses lithium-containing materials such as betalite and clay raw materials that are comparable to ordinary porcelain in terms of mechanical strength, corrosion resistance, and plastic moldability, and have excellent properties in terms of heat resistance. The present invention relates to the improvement of low thermal expansion porcelain compositions, and in particular, to widen the firing temperature range to obtain industrially advantageous low thermal expansion porcelain.
なおここで用いた焼成温度範囲というのは焼結体の吸水
率がほぼ0%で、収縮の増加と形状の軟化のみとめられ
ない領域とした。従来、低熱膨脹性を示し耐熱性磁器と
して利用される倉リチウム物質素地はべ夕ライト等の含
リチウム物質と可塑性向上のための粘土質材料を配合す
るのが普通である。The firing temperature range used here was a range in which the water absorption rate of the sintered body was approximately 0% and no increase in shrinkage or softening of the shape could be observed. Conventionally, the lithium material base material, which exhibits low thermal expansion and is used as heat-resistant porcelain, is usually blended with a lithium-containing material such as bayite and a clay material to improve plasticity.
ところがこの含リチウム物質素地は焼成温度範囲が20
o0程度と狭く近年の窯炉の大型化にともなう焼成温度
の制御の困難さを考えると少なくとも40oo以上の焼
成温度範囲がなければ工業的な生産は困難となって来て
いた。そこでこの焼成温度範囲を拡大するための種々の
研究が行われていたが工業的に有利な方法でこの問題を
解決するには至っていない。また一方、コージラィト素
地など比較的低熱堀彰眼性磁器に用いられる柚薬の研究
も進められており本発明者はこの柚薬として7山203
・56.$i02・狐Nao・母けg0・Xaoの如き
アルカリ及びアルカリ士金属酸化物を含む調合物が有効
であると見いだし、更にこの調合物が前述の焼成温度範
囲拡大に寄与することを見いだして本発明をするに至つ
た。However, this lithium-containing material base has a firing temperature range of 20
Considering the difficulty in controlling the firing temperature as kilns have become larger in recent years, industrial production has become difficult unless there is a firing temperature range of at least 40 oo. Various studies have been conducted to expand this firing temperature range, but this problem has not yet been solved by an industrially advantageous method. On the other hand, research is also progressing on yuzu medicine used in relatively low-temperature Hori Shogen porcelain such as cordierite base material, and the present inventor has proposed that this yuzu medicine can be used in 7 mountains 203.
・56. We have found that formulations containing alkali and alkali metal oxides such as $i02, Kitsune Nao, Mokke g0, and Xao are effective, and furthermore, we have discovered that this formulation contributes to expanding the firing temperature range mentioned above, and have published this book. I came up with an invention.
すなわち、本発明は含リチウム物質30〜60%と粘土
質原料20〜60%とよりなる低熱膨脹性磁器の配合原
料に長石23.0%、珪石31.5%、タルク15.4
%、石灰石4.0%、カオリン26.2%を含む調合物
10〜40%配合して1220〜1340q0で焼成し
てその焼成温度範囲を40oo〜60午0程度とかなり
拡大できるようにして、工業的に有利な低熱膨脹性磁器
組成物である。That is, in the present invention, 23.0% of feldspar, 31.5% of silica, and 15.4% of talc are added to the raw materials for low thermal expansion porcelain, which is composed of 30 to 60% of lithium-containing material and 20 to 60% of clay material.
%, limestone 4.0%, and kaolin 26.2% by 10 to 40%, and fired at 1220 to 1340q0, so that the firing temperature range can be considerably expanded to about 4000 to 60000. It is an industrially advantageous low thermal expansion porcelain composition.
本発明において焼成温度範囲拡大のために添加すべきア
ルカリ及びアルカリ士金属酸化物を含む調合物は7AI
203・56.$j02・狐Nao・QMg○・Xa○
の如きものがよい。In the present invention, the formulation containing alkali and alkali metal oxides to be added to expand the firing temperature range is 7AI.
203・56. $j02・Fox Nao・QMg○・Xa○
Something like this is good.
次に配合すべき原料としては、含リチウム物質物質の原
料にべタラィトを粘土質原料に蛙目粘士あるいは木節粘
土を用いればよく、またアルカリ及びアルカリ士金属酸
化物を含む調合物は、シリカの原料に桂石を、アルミナ
の原料にカオリンを酸化カルシウムの原料に石灰石を、
酸化マグネシウムの原料にタルクあるいはマグネサィト
を、酸化カリウム及び酸化ナトリウムの原料に長石を用
いればよい。Next, as the raw materials to be blended, Betalite may be used as the raw material for the lithium-containing substance, and Frogme clay or Kibushi clay may be used as the clayey raw material.For a mixture containing an alkali and an alkali metal oxide, Katsuraite is the raw material for silica, kaolin is the raw material for alumina, limestone is the raw material for calcium oxide,
Talc or magnesite may be used as a raw material for magnesium oxide, and feldspar may be used as a raw material for potassium oxide and sodium oxide.
またアルカリ及びアルカリ土金属酸化物を含む調合物は
上記原料を長石23.0%、桂石31.5%、タルク1
5.4%、石灰石4.0%、朝鮮カオリン26.2%(
Wt.%)とすればよく、この調合物をWt.%でべタ
ラィト30〜60%、粘土質原料20〜60%とともに
10〜40%配合すればよい。In addition, a formulation containing alkali and alkaline earth metal oxides is made by combining the above raw materials with 23.0% feldspar, 31.5% laurel, and 1 talc.
5.4%, limestone 4.0%, Korean kaolin 26.2% (
Wt. %), and this formulation can be expressed as Wt. It is sufficient to mix 10 to 40% of betalite with 30 to 60% of betalite and 20 to 60% of clay raw material.
実施例 1
べタライト40%、原蛙目粘土40%、井上長石4.6
%、石6.3%、タルク3.1%、石灰石0.8%、朝
鮮カオリン5.24%(Wt.%)を配合して化学組成
がSi。Example 1 40% Betalite, 40% Frog-eye clay, 4.6 Inoue feldspar
%, stone 6.3%, talc 3.1%, limestone 0.8%, and Korean kaolin 5.24% (Wt.%), and the chemical composition is Si.
267・87%、N2031892%、Fe2030・
49%、Ti020.斑%、Mg01.26%、Ca0
0.86%、K201.16%、Na00.75%、L
i201.74%、灼熱減量665%(Wt.%)にな
るようにし、ポットミルで4時間湿式混合縄梓後脱水し
て適当な可塑性を有する坪土に調整し、これを真空押出
機で170×17仇h/mの試験棒を作り乾燥後ェレマ
発熱体電気炉により加熱速度5℃/min最高温度保持
時間1時間で処理後炉内で自然放冷してその物理試験等
を行なつoなお最高処理温度を120000毎に変化さ
せ130ぴCまで変化させた各々の試料により隣結の度
合を知り焼成温度範囲を知ることができる。267.87%, N2031892%, Fe2030.
49%, Ti020. Spot%, Mg01.26%, Ca0
0.86%, K20 1.16%, Na00.75%, L
i201.74%, loss on ignition 665% (Wt.%), wet-mixed in a pot mill for 4 hours, dehydrated and adjusted to a tsubo soil with appropriate plasticity, and then mixed in a vacuum extruder at 170× A test bar of 17 h/m was prepared, dried, and then treated in an electric furnace with heating element heating element at a heating rate of 5°C/min and a maximum temperature holding time of 1 hour.After that, it was allowed to cool naturally in the furnace and physical tests were performed on it. By changing the maximum processing temperature in steps of 120,000 to 130 picoC, the degree of adjacency can be determined and the firing temperature range can be determined.
試験の結果は次の通りである。第 1 表
このように吸水率は122ぴ○〜128ぴ0までほぼ0
%となり軟化もなく、この間60℃が完全に磁化される
範囲ということができる。The test results are as follows. Table 1 As shown, the water absorption rate is almost 0 from 122 pi○ to 128 pi 0.
%, and there is no softening, and 60° C. can be said to be the range of complete magnetization during this period.
次に、三成分系組成図の数部分について吸水率、熱駒鞍
張係数、嫌成範囲、化学組成を示して焼成温度範囲40
℃〜60ooの最適範囲を示す。Next, we will show the water absorption rate, thermal tension coefficient, anaerobic range, and chemical composition for several parts of the ternary composition diagram.
The optimum range of ℃~60oo is shown.
ここで調合物とは前記のアルカリ及びアルカリ士金属酸
化物を含む調合物を言い、番号は三成分系組成図中の番
号と一致する。船
澱
級上の如く、ベタラィトが60%より多くなれば暁結温
度が高くなり例えば図の■の如く1私ぴ0以上で高温で
ありしかも、135ぴ0以上では軟化するため結局焼成
温度範囲は10qoと極めて狭いものとなる。The formulation herein refers to a formulation containing the alkali and alkali metal oxides described above, and the numbers correspond to the numbers in the ternary composition diagram. As shown in the ship's starch grade, if betalite is more than 60%, the dawning temperature will be high.For example, as shown in the figure (■), the temperature is high above 100%, and it softens above 1350%, so the sintering temperature range will eventually change. is extremely narrow at 10 qo.
又一方べタラィトを30%より少くすると図中10,1
1,12に示す如く熱膨脹係数は4×10‐6以上と大
きく低熱膨脹性磁器としては不適であり、その焼成温度
範囲も2ぴ0と狭い。また粘土分が20%以下となって
も図中5,9に示す如く糠成温度範囲1000〜20q
0と狭く工業的に利用し難いものである。同様に調合物
を10%より少くあるいは40%より多い場合も図中4
,10あるいは9,12に示す如く焼成温度範囲は1ぴ
0〜2ぴ0となり同機の結果となる。On the other hand, if betalite is reduced to less than 30%, it becomes 10,1 in the figure.
As shown in Nos. 1 and 12, the coefficient of thermal expansion is large, 4×10-6 or more, making it unsuitable as a low thermal expansion porcelain, and the firing temperature range is narrow, at 2.0. Furthermore, even if the clay content is less than 20%, the braning temperature range is 1000~20q as shown in 5 and 9 in the figure.
0, making it difficult to use industrially. Similarly, if the mixture is less than 10% or more than 40%, 4 in the figure
, 10 or 9, 12, the firing temperature range is 1pi0 to 2pi0, which is the result of the same machine.
縞局べタラィト30〜60%、粘土質原料20〜60%
、調合物10〜40%とした場合は図中2,3,6,7
,8に示す如く熱膨脹係数は1〜3.5×10‐6と低
く更に焼成温度範囲が40℃〜60qo程度と競成時の
窯炉の制御が容易となり工業的に有利な低熱膨脹性磁器
組成物を得ることができる。Striped betalite 30-60%, clay raw material 20-60%
, 2, 3, 6, 7 in the figure when the formulation is 10 to 40%.
, 8, the coefficient of thermal expansion is as low as 1 to 3.5 x 10-6, and the firing temperature range is approximately 40°C to 60qo, making it easy to control the kiln during production, making it an industrially advantageous low thermal expansion porcelain. A composition can be obtained.
第1図は本発明に配合する調合物のみの鱗鯖体の温度‐
熱膨脹率のグラフ、又第2図は調合物のX線解析線図、
第3図はべタラィト、粘士、調合物の三成分系組成図。
オー図オ之図
外3図Figure 1 shows the temperature of the mackerel body of only the formulation blended in the present invention.
A graph of the coefficient of thermal expansion, and Figure 2 is an X-ray analysis diagram of the formulation.
Figure 3 is a three-component system composition diagram of betalite, viscosity, and a compound. 3 diagrams outside the diagram
Claims (1)
粘土質原料20〜60%よりなる配合原料に焼成温度範
囲拡大のための添加物として、長石23.0%、珪石3
1.5%、タルク15.4%石灰石4.0%、カオリン
26.2%を含む調合物を10〜40%(Wt%)配合
し、1220〜1340℃で焼成してなる低熱膨脹性磁
器組成物。30-60% fine powder of lithium-containing materials such as petalite,
As additives to expand the firing temperature range, feldspar 23.0% and silica stone 3
Low thermal expansion porcelain made by blending 10 to 40% (wt%) of a formulation containing 1.5% talc, 15.4% limestone, and 26.2% kaolin and firing at 1220 to 1340°C. Composition.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51120902A JPS6020342B2 (en) | 1976-10-06 | 1976-10-06 | Low thermal expansion porcelain composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51120902A JPS6020342B2 (en) | 1976-10-06 | 1976-10-06 | Low thermal expansion porcelain composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5345311A JPS5345311A (en) | 1978-04-24 |
| JPS6020342B2 true JPS6020342B2 (en) | 1985-05-21 |
Family
ID=14797815
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP51120902A Expired JPS6020342B2 (en) | 1976-10-06 | 1976-10-06 | Low thermal expansion porcelain composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6020342B2 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6846768B1 (en) * | 2003-03-26 | 2005-01-25 | Carlisle Foodservice Products, Incorporated | Methods and compositions for low thermal expansion ceramic |
| JP6918351B2 (en) * | 2017-07-14 | 2021-08-11 | 株式会社チップトン | Ceramic member and flow path member |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2919995A (en) * | 1958-02-12 | 1960-01-05 | Corning Glass Works | Low expansion ceramic body and a method of making it |
-
1976
- 1976-10-06 JP JP51120902A patent/JPS6020342B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5345311A (en) | 1978-04-24 |
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