JPS58101006A - Casting molding method for ceramic product - Google Patents

Casting molding method for ceramic product

Info

Publication number
JPS58101006A
JPS58101006A JP56200675A JP20067581A JPS58101006A JP S58101006 A JPS58101006 A JP S58101006A JP 56200675 A JP56200675 A JP 56200675A JP 20067581 A JP20067581 A JP 20067581A JP S58101006 A JPS58101006 A JP S58101006A
Authority
JP
Japan
Prior art keywords
parts
slurry
molding method
ceramic product
casting molding
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.)
Pending
Application number
JP56200675A
Other languages
Japanese (ja)
Inventor
稔也 田中
斉藤 和美
南里 隼人
金子 泰成
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.)
Taiko Refractories Co Ltd
Original Assignee
Taiko Refractories Co 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 Taiko Refractories Co Ltd filed Critical Taiko Refractories Co Ltd
Priority to JP56200675A priority Critical patent/JPS58101006A/en
Publication of JPS58101006A publication Critical patent/JPS58101006A/en
Pending legal-status Critical Current

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  • Compositions Of Oxide Ceramics (AREA)
  • Producing Shaped Articles From Materials (AREA)

Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 なセラミック製品の鋳込み成形方法に関するものである
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a casting method for ceramic products.

鋳込み成形法は古くから陶磁器、食器、微生陶器をはじ
め理化学用セラミックなどの成形に広く利用されており
、セラミック製品の成形法としては最も一般的である。
The cast molding method has been widely used for molding ceramics, tableware, microporcelain, and ceramics for physical and chemical use since ancient times, and is the most common method for molding ceramic products.

粉体は水中で電荷をおびているが、特定のPHでは■に
もOKも電荷をおびない所(これを等電点という)があ
る。安定な泥漿を作るためには、この等電点が関与する
。即ち、PHをHclやNaOHで酸性やアルカリ性に
調整することで粉体表面に電荷を与え、電荷間の反発で
2次粒子を1次粒子化して解膠させるのが従来の鋳込み
成形方法である0がしかし、従来法は酸性やアルカリ性
で泥漿を作り型枠に鋳込むために泥漿と型枠との反応に
より型枠が損耗して寿命が短かくなり、成形品の寸法精
度が悪くなるという欠点がある。
Powder is charged in water, but at certain pHs there is a point where neither ■ nor OK is charged (this is called the isoelectric point). This isoelectric point is involved in creating a stable slurry. In other words, in the conventional casting molding method, the pH is adjusted to acidic or alkaline with HCl or NaOH to give an electric charge to the powder surface, and the repulsion between the electric charges causes the secondary particles to become primary particles and peptize. However, in the conventional method, slurry is created using acidic or alkaline conditions and poured into the mold, and the reaction between the slurry and the mold causes wear and tear on the mold, shortening its lifespan and reducing the dimensional accuracy of the molded product. There are drawbacks.

これに対し、泥漿を中性として鋳込み成形するいわゆる
中性鋳込み成形方法は、1配した酸性やアルカリ性で鋳
込み成形した場合の様な型枠との反応による型枠の損耗
が非常に小さいという長所を有している。しかし、中性
鋳込み成形方法では等電点が中性域にあるもの(例えば
アルミナ、ジルコニア、酸化クロム、酸化チタンなど)
はHcjやNaOHを用いてPR調整しても電荷間の反
発が非常に小さく、粒子がうまく解膠しないため鋳込み
成形できなかった。
On the other hand, the so-called neutral casting method, in which slurry is cast in a neutral slurry, has the advantage that there is very little wear and tear on the formwork due to reaction with the formwork, which is the case when casting is carried out in an acidic or alkaline solution. have. However, in the neutral casting method, materials whose isoelectric points are in the neutral range (e.g. alumina, zirconia, chromium oxide, titanium oxide, etc.)
Even if PR was adjusted using Hcj or NaOH, the repulsion between the charges was very small, and the particles did not deflocculate well, so casting could not be performed.

本発明者らは、中性鋳込み成形方法を可能にするため神
々検討し、本発明をなし得たものである。
The present inventors have made extensive studies to enable a neutral cast molding method, and have accomplished the present invention.

その要旨とするところは、セラミック粉体に対して解膠
剤と1でポリアクリル酸オリゴマーまたはポリアクリル
酸オリゴマーのアンモニウム塩(共に分子置約3000
〜12000)と有機結合剤と水を混治し、泥漿を中性
としたことを特徴とするセラミック極品の鋳込み成形方
法にある。
The gist of this is that a polyacrylic acid oligomer or an ammonium salt of a polyacrylic acid oligomer (both with a molecular size of about 3000
12,000), an organic binder, and water to make the slurry neutral.

本発明の対象となるセラミック粉体は、アルミナ、酸化
チタン、チタン酸バリウム、ジルコン、ジルコニア、ス
ピネルなどの酸化物をはじめ、炭化珪素、窒化珪素など
の炭化物、窒化物にも適用できる。
Ceramic powders to which the present invention is applicable include oxides such as alumina, titanium oxide, barium titanate, zircon, zirconia, and spinel, as well as carbides and nitrides such as silicon carbide and silicon nitride.

本発明における構成要素の一つである解膠剤としてはポ
リアクリル酸オリゴマーまたはこのオリゴマーヲ液体ア
ンモニア、アンモニア水で中和したアンモニウム塩を粉
体の柚類により使い分ける。
As the deflocculant, which is one of the constituent elements of the present invention, polyacrylic acid oligomer or ammonium salt obtained by neutralizing this oligomer with liquid ammonia or aqueous ammonia is used depending on the powder of yuzu.

ポリアクリル酸オリゴマーは水中で HcjやNaOHのような単分子と異なり、ポリアクリ
ル酸オリゴマーは分子量が大きく、分子構造が適当に大
きいので水和膜中に入りこむことはなく、もし入っても
+OH,−CjH+構造の疎液性と000の組液性が分
子内に存在するために粉体表面を安定化する働きをする
0ゆえに、ポリアクリル酸オリゴマーは水中ではPHを
容易に中性に保つことができ、凝集を起さずに粉体の等
電点に関係なく解膠状態を保持できるという性質を有し
ている。
Unlike single molecules such as Hcj and NaOH, polyacrylic acid oligomers have a large molecular weight and a suitably large molecular structure in water, so they do not enter the hydrated film, and even if they do, +OH, The lyophobicity of the -CjH+ structure and the lyotropic property of 000 present in the molecule work to stabilize the powder surface, so polyacrylic acid oligomers can easily keep the pH neutral in water. It has the property of being able to maintain a peptized state regardless of the isoelectric point of the powder without causing agglomeration.

ポリアクリル酸オリゴマーまたはポリアクリル酸オリゴ
マーのアンモニウム塩の分子量を3000〜] 200
0に限定したのは、分子量が3000以下のものはセラ
ミック粉体に対して解膠作用のみを示し、粒子の沈降を
防止する作用は全くなく、逆に沈降を促進し、長時間た
つと解膠した粒子がまた凝集してしまう。また1200
0以上になると解膠作用が弱く、粉体粒子間を結びつけ
る結合力が大きいという理由からである。
The molecular weight of polyacrylic acid oligomer or ammonium salt of polyacrylic acid oligomer is 3000~] 200
The reason why we limited it to 0 is because those with a molecular weight of 3000 or less only have a peptizing effect on ceramic powder, have no effect at all to prevent particle sedimentation, and on the contrary promote sedimentation and cause decomposition over a long period of time. The sticky particles will coagulate again. 1200 again
This is because when it is 0 or more, the peptizing effect is weak and the bonding force that binds the powder particles is large.

本発明の解−剤の添加量はセラミック粉体】00部に対
して0.2〜2.5部、特には0.4〜1.5部が好ま
しい00.2部以下では解膠剤としての効果がなく、泥
漿がうまく解膠しない。また2、5部以上では解膠性は
殆んど変わらず、逆に焼結体の密度に悪影響を及ぼす。
The amount of the deflocculant added in the present invention is preferably 0.2 to 2.5 parts, particularly 0.4 to 1.5 parts, and preferably 0.4 to 1.5 parts or less, as a peptizer based on 0.00 parts of the ceramic powder. is not effective and the slurry does not deflocculate well. Moreover, if it exceeds 2.5 parts, the peptizing property will hardly change, and the density of the sintered body will be adversely affected.

もう一つの構成要素である有機結合剤は成形体の強度を
付与するもので、ポリビニルアルコール、デンプン、ポ
リビニルピロリドン、水溶性アクリル系ポリマー、グリ
セリンなどの多価アルコール、メチルセルロース、ゼラ
チンなどが用いられる。
The organic binder, which is another component, imparts strength to the molded product, and includes polyvinyl alcohol, starch, polyvinylpyrrolidone, water-soluble acrylic polymers, polyhydric alcohols such as glycerin, methylcellulose, gelatin, and the like.

添加量はセラミック粉体100部に対して0.01〜2
.0部、特には0.05〜1.0部が好ましい。
The amount added is 0.01 to 2 parts per 100 parts of ceramic powder.
.. 0 part, especially 0.05 to 1.0 part is preferred.

0.01部以下では結合剤としての効果がなく、成形体
の強度が得られない。また2、0部以上では強度の増大
はあまり認められず、乾燥条件などに悪影響を及ぼす。
If it is less than 0.01 part, it will not be effective as a binder and the strength of the molded article will not be obtained. Further, if the amount is 2.0 parts or more, no significant increase in strength is observed, which adversely affects drying conditions.

また泥漿の粘性の安定性を高めたり、着肉速度を調整し
たり、脱型性を良好にする目的で必要があれば保論コロ
イドや湿潤剤などを添加することも目■能である。
It is also possible to add colloids, wetting agents, etc., if necessary, for the purpose of increasing the stability of the viscosity of the slurry, adjusting the deposition rate, or improving demoldability.

以下に実施例を挙げて説明を捕足するが、一本発明はこ
の実施例にのみ限定されるものではない。
The following description will be given with reference to examples; however, the present invention is not limited to these examples.

実施例1 77Mす粉体(純度99.5%、平均粒径0.5Aa3
100部に対して水35部と解膠剤としてポリアクリル
酸オリゴマー(分子量5500)0.44ffl有機結
合剤としてポリビニルアルコール(重合度500 ) 
0.15部、m*剤としてシリコンポリエーテル系ノニ
オン活性剤を0.08部加えてボールミルで6時間攪拌
し均一な泥漿を作った。この泥漿を146φ×120鴎
の型枠に鋳込み3,0分間放置する。その後説枠して6
0℃で2時間乾燥後、さらに120℃で2時間乾燥後、
8時間で1600℃に昇温し、1600℃で2時間保持
後放冷した。以上の本発明方法と酸性鋳込み成形方法を
表1に比較して示す。
Example 1 77M powder (purity 99.5%, average particle size 0.5Aa3
35 parts of water per 100 parts, 0.44 ffl of polyacrylic acid oligomer (molecular weight 5500) as a deflocculant, and polyvinyl alcohol (degree of polymerization 500) as an organic binder.
0.15 parts and 0.08 parts of a silicone polyether nonionic activator as an m* agent were added and stirred in a ball mill for 6 hours to form a uniform slurry. This slurry was cast into a 146φ x 120 mold and left for 3.0 minutes. After that, the frame is 6
After drying at 0°C for 2 hours, and then at 120°C for 2 hours,
The temperature was raised to 1600°C over 8 hours, maintained at 1600°C for 2 hours, and then allowed to cool. Table 1 shows a comparison between the method of the present invention and the acid casting method described above.

表  1 型枠損耗度は侵食厚/使用回数で表わしたものである。Table 1 The degree of formwork wear is expressed as erosion thickness/number of uses.

実施例2 イツトリア3mo 1%で安定化したジルコニア粉体(
粒径0.3部%)100部に対して水40部と解−剤と
してポリアクリル酸オリゴマーのアンモニウム塩(分子
量5500 ) 1.5部、有機結合剤としてメトキシ
メチルメタアクリレートとアクリル銀との共重合体(分
子量20000 J O,4部、湿潤剤としてポリアル
キレン系誘導体を0.]部加えてボールミルで6時間攪
拌して均一な泥漿を作つた。この泥漿をl0IIIII
XIOIIIIX100IIIIBの型枠に流し込んで
50分間放置後説枠し、60℃で2時間乾燥後、さらに
120℃で2時間乾燥後8時間で1600℃まで昇温し
、1600℃で2時間保持後放冷した。以上の本発明方
法とアルカリ性鋳込み成形方法を表2に比較して示す0
表  2 以上の実施例から本発明は従来の鋳込み成形方法に較べ
て型枠の寿命が向上し、しかも焼結体の機械的性質に優
れるという特徴を有するセラミック製品の鋳込み成形方
法であることが明らかであるO
Example 2 Zirconia powder stabilized with Ittria 3mo 1% (
40 parts of water, 1.5 parts of ammonium salt of polyacrylic acid oligomer (molecular weight 5500) as a peptizer, methoxymethyl methacrylate and acrylic silver as an organic binder, per 100 parts (particle size: 0.3 parts%). A copolymer (4 parts of molecular weight 20,000 JO, 0.] part of a polyalkylene derivative as a wetting agent) was added and stirred in a ball mill for 6 hours to make a uniform slurry.
Pour into a mold of XIOIII did. Table 2 shows a comparison of the above method of the present invention and the alkaline casting method.
Table 2 From the above examples, it can be seen that the present invention is a method for casting ceramic products, which has the characteristics that the life of the mold is improved compared to the conventional casting method, and the mechanical properties of the sintered body are excellent. O is obvious

Claims (1)

【特許請求の範囲】[Claims] (1)  セラミック粉体に対して、解膠剤としてポリ
、アクリル酸オリゴマーまたはポリアクリル酪オリゴマ
ーのアンモニウム塩(共に分子量約3000〜3200
0)と有機結合剤と水を混合し、泥漿を中性としたこと
を特徴とするセラミック製品の鋳込み成形方法。
(1) Ammonium salts of poly, acrylic acid oligomers or polyacrylic butyric oligomers (both with molecular weights of about 3000 to 3200) are used as deflocculants for ceramic powder.
0), an organic binder, and water to make the slurry neutral.
JP56200675A 1981-12-11 1981-12-11 Casting molding method for ceramic product Pending JPS58101006A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP56200675A JPS58101006A (en) 1981-12-11 1981-12-11 Casting molding method for ceramic product

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP56200675A JPS58101006A (en) 1981-12-11 1981-12-11 Casting molding method for ceramic product

Publications (1)

Publication Number Publication Date
JPS58101006A true JPS58101006A (en) 1983-06-16

Family

ID=16428366

Family Applications (1)

Application Number Title Priority Date Filing Date
JP56200675A Pending JPS58101006A (en) 1981-12-11 1981-12-11 Casting molding method for ceramic product

Country Status (1)

Country Link
JP (1) JPS58101006A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61202804A (en) * 1985-03-06 1986-09-08 キヤタラ−工業株式会社 Muddy casting molding method of silicon nitride ceramics
JPS61233503A (en) * 1985-03-28 1986-10-17 キヤタラ−工業株式会社 Slurry casting molding method of silicon nitride ceramics
JPH01222902A (en) * 1988-03-02 1989-09-06 Toshiba Ceramics Co Ltd Ceramic hollow body, its manufacture and ceramic ball for valve
US5342563A (en) * 1991-11-22 1994-08-30 The Lubrizol Corporation Methods of preparing sintered shapes and green bodies used therein

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61202804A (en) * 1985-03-06 1986-09-08 キヤタラ−工業株式会社 Muddy casting molding method of silicon nitride ceramics
JPS61233503A (en) * 1985-03-28 1986-10-17 キヤタラ−工業株式会社 Slurry casting molding method of silicon nitride ceramics
JPH01222902A (en) * 1988-03-02 1989-09-06 Toshiba Ceramics Co Ltd Ceramic hollow body, its manufacture and ceramic ball for valve
US5342563A (en) * 1991-11-22 1994-08-30 The Lubrizol Corporation Methods of preparing sintered shapes and green bodies used therein
US5585428A (en) * 1991-11-22 1996-12-17 The Lubrizol Corporation Green bodies formed from inorganic powders and a carboxylic acylating agent

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