JPS59199570A - Ceramic forming composition and dewaxing process - Google Patents

Ceramic forming composition and dewaxing process

Info

Publication number
JPS59199570A
JPS59199570A JP58075377A JP7537783A JPS59199570A JP S59199570 A JPS59199570 A JP S59199570A JP 58075377 A JP58075377 A JP 58075377A JP 7537783 A JP7537783 A JP 7537783A JP S59199570 A JPS59199570 A JP S59199570A
Authority
JP
Japan
Prior art keywords
ceramic
forming composition
degreasing
dewaxing process
ceramic forming
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
JP58075377A
Other languages
Japanese (ja)
Inventor
岩田 幸一
西本 達也
英雄 高橋
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.)
Sumitomo Electric Industries Ltd
Original Assignee
Sumitomo Electric Industries 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 Sumitomo Electric Industries Ltd filed Critical Sumitomo Electric Industries Ltd
Priority to JP58075377A priority Critical patent/JPS59199570A/en
Publication of JPS59199570A publication Critical patent/JPS59199570A/en
Pending legal-status Critical Current

Links

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】 (イ)技術分野 本発明は各種セラミック製品を押出成形あるいは射出成
形するためのセラミック成形用、i、ll bM 物1
1に。
Detailed Description of the Invention (a) Technical field The present invention relates to ceramic molding for extrusion molding or injection molding various ceramic products.
To 1.

ひに脱脂方法に関するものであり、成形後の成ハタ体か
ら新規な方法で有(浅成分を除去するものである。
This relates to a method for degreasing seaweed, which involves removing superficial components from the molded grouper body using a novel method.

(ロ)発明の背景 近年その優れた高温強度の為は構;1s品へのニューセ
ラミックス(以下11iにセラミックと記す)の用途が
拡大している。その成形方法としては従来のホットプレ
ス、静圧プレスといっブこ加圧bE Il’3に加え、
複全11な形状でも成形可能なこと、及び生産コストか
廉価なことから押出成形あるいは射出成形といった可塑
成形法が次第に)1イ及しつつある。
(B) Background of the Invention In recent years, the use of new ceramics (hereinafter referred to as 11i as ceramics) for 1s products has been expanding due to their excellent high-temperature strength. In addition to the conventional hot press, static pressure press, and press bE Il'3, the molding method is
Plastic molding methods such as extrusion molding and injection molding are gradually becoming popular because they can be molded into complex shapes and are inexpensive to produce.

これらの可塑成形を行なう為には本来、11J qjl
川牛用持たないセラミック粉体に流動izl: 、 1
llll:形計をイ」与する為に有機バインダーを添加
しなければならない。従来この有機バインダーとしてス
チレン系1ろj脂、オレフィン系樹脂、ポリブテン、メ
チルメタアクリレ−1・、エポキシ樹脂、フェノールt
VJ脂。
In order to perform these plastic moldings, originally 11J qjl
Ceramic powder that does not have fluidity for river cattle: 1
llll: An organic binder must be added to give the shape. Conventionally, organic binders such as styrene resin, olefin resin, polybutene, methyl methacrylate, epoxy resin, and phenol have been used as organic binders.
VJ fat.

パラフィン、ワックス等が1史川されているか、成jは
後にセラしツク成形体から有(3成分を除去する1i(
a脂1.程に大きなり111点があった。即ち、従来の
脱脂l’、 i”+”では、老ラミック成形体を甲、に
加熱し、有(政1戊分を加ゼ1分解させて除去する為、
分解ガスによるフクレ、キレソが生じない様に極めてゆ
るやかにy邑ill!させ数1′から数百時間かけて脱
脂処理を1」すっテイタ。尚がっ脱指後の成形品にフク
レ。
If paraffin, wax, etc. are removed from the molded body, it is later removed from the ceramic molded body (1i) to remove the three components.
a fat 1. There was a huge score of 111 points. That is, in the conventional degreasing method, the old ramic molded body is heated to a high temperature, and the laminate is removed by decomposing it.
Rinse very gently so as not to cause blisters or cracks due to decomposed gas! The degreasing process takes anywhere from several minutes to several hundred hours. Blisters appear on the molded product after removing fingers.

キレンの生じる頻度は比較的高く、工業的に満足し得る
方法とは苦い、ゴ[がった。
The frequency of generation of oxidation is relatively high, and there is no industrially satisfactory method for producing it.

(ハ) 発明の構成 熱手段とを併用することにより、比較的短時間でフクレ
、キレッ等の生じないセラミック成形用組成1勿及び脱
脂方法を見い出したものである。脱脂l: f’+’、
において重要なことはセラミック成形体の表面からイJ
()成分を分解ガスとして徐々に揮11夕せしめ、Il
[+’i次内部へと分解を進行させることにある。
(c) By using the heating means of the invention in combination, we have discovered a composition for ceramic molding and a degreasing method that does not cause blisters, cracks, etc. in a relatively short period of time. Degreasing l: f'+',
What is important is that the surface of the ceramic molded body is
The components () are gradually vaporized as a decomposed gas, and the Il
The purpose is to proceed with the decomposition to the +'i-order interior.

甲に加熱ト!没のみを用いる方法では、この分解の進行
を制御卸することは非常に回加であるか、不発明の方法
によれば容易にセラ< ツク成形体の表は電子線を照射
すると、これらの線量は照射面で起こり、順次内部へと
分解は移行し発生した分解ガスは既に形成されたミクロ
パスを通して揮1牧する。しかる後に残余の有機バイン
ダー成分を加熱脱脂すると、照射によって形成されたミ
クロバスが成形体内部から表面にかけて存在しているの
で、発生じたガスの内部にょるフクレ、キレソを生ぜメ
チル基を有するポリマーであり、具体的には、ポリプロ
ピレン7 ポリイソブチレン、ポリメタクリレ−1・、
ポリα−メチルスチレン等をあげることぞC ができる。これらのポリマーは、砦外線あるいは電子線
によってメチル基と結合しているイぐ斉炭素原子に遊離
ラジカルがブこ生し、例えばポリプロピレンてはドに示
すようなラジカル崩壊が発生する。
Heat the instep! In the method using only molten metal, controlling the progress of this decomposition is very repetitive, but in the uninvented method, it is easy to control the progress of this decomposition. The dose occurs on the irradiated surface, and the decomposition gradually moves to the inside, and the generated decomposed gas evaporates through the already formed micropaths. When the remaining organic binder component is then heated and degreased, the microbaths formed by the irradiation are present from the inside of the molded product to the surface, so the generated gas causes blisters and creases inside the molded product, resulting in polymers with methyl groups. Yes, specifically, polypropylene 7, polyisobutylene, polymethacrylate 1,
Poly-alpha-methylstyrene and the like can be used as examples. In these polymers, free radicals are generated at the ionic carbon atoms bonded to methyl groups by external radiation or electron beams, and for example, in polypropylene, radical decay as shown in (d) occurs.

左側は崩壊l)i+であり、右側は崩壊後の形を示す。The left side shows the collapse l)i+, and the right side shows the form after collapse.

〜C1l 2 C−C112−CI−T〜−2〜CI−
I 2−C= CI−I 2+・CH〜1    ’l
       l     1CI−Tろ  CI5 
    CH3C!(3啼 これら檗外線崩壊型樹脂は、単独でセラミックの有(幾
バインダーとして用いることも出来るが、セラミック粉
末との親和12+を高め、成形時の流動性を高める為に
は、他の公知の有椴バインダーと組み合わせることも出
来る。その他の1+、+17成材料としでは既存のlj
;j料を適宜組み合わせて用いることが出来る。即ちセ
ラミック粉末としては、アルミ九酸化ノルコン、望化ア
ルミ、窒化珪素、炭化珪素やあるいはタングステンカー
バイド等の超硬合金やサーメットを用いることが出来、
焼結助剤としではマグネシア、アルミナ、酸化イツトリ
ウム。
~C1l2C-C112-CI-T~-2~CI-
I2-C=CI-I2+・CH~1'l
l 1CI-Tro CI5
CH3C! (3) These outer-line collapsible resins can be used alone as a ceramic binder, but in order to increase the affinity with ceramic powder (12+) and improve the fluidity during molding, it is necessary to use other known It can also be combined with Arisa binder.Other 1+ and +17 materials include existing lj
;J ingredients can be used in appropriate combination. That is, as the ceramic powder, a cemented carbide or cermet such as aluminum nonaoxide, aluminum oxide, silicon nitride, silicon carbide, or tungsten carbide can be used.
Sintering aids include magnesia, alumina, and yttrium oxide.

La系1唆化物、ボロンカーバイド、鉄属金属等を猶げ
ることが出来る。又加工助剤として、公知り分:”、y
、”’J f’、lJ 、滑i’jlj 、に:E!v
r’i i+Jが用いられ、飽和脂肪1−1不(・a和
°[11肪)、金属石ケン、高j汲アルコール、動植物
油。
La-based monoxides, boron carbide, ferrous metals, etc. can be contained. Also known as a processing aid: ", y
,”'J f', lJ, slipi'jlj, ni:E!v
r'i i+J is used, saturated fat 1-1 fat (・a sum ° [11 fat), metal soap, high-j alcohol, animal and vegetable oil.

鉱物油5合成エステル油等を使用することが出来る。以
下に実施例をあげて本発明の効果を小す。
Mineral oil, synthetic ester oil, etc. can be used. Examples are given below to reduce the effects of the present invention.

に)実施例 実施例1 窒化珪素粉末100 ’U j、、+に部に対し、マグ
ネシアを4重量部、ステアリン酸を2屯11(部、パラ
フィンを4重量部、低密度ポリエチレンを20重11(
部及び紫外線崩壊型樹脂としてポリイソフチシン4重h
−(部とを添加混合し、溶盗混練りした後、粉砕してフ
レーク状とし、このものを射出成形膜にて、5 X 1
2X 40 mrnのセラミック成;1ヨ体を出た。次
にこのセラミック成形体の脱脂工程として、波長掌 域600〜4 口Q nmの紫外線照射を10分間行な
つ滅 た。この紫外線強度は20111″w/A・rjiであ
った。し7かる後に、加熱による脱脂処理を1Jなった
。セラ(ツク成形体にフクレ、キレッ′3を生じさせず
に脱脂出来る条j牛は、200℃−2Hr−250℃−
41−I r−350℃−4Hr−500℃−4Hrで
あった。このようにして脱脂処理を行なったセラE ツ
ク成形体を、1700’C−12Hrで焼結し、セラミ
ックD’を結体を得た。
Examples Example 1 For 100 parts of silicon nitride powder, 4 parts by weight of magnesia, 2 parts by weight of stearic acid, 11 parts by weight of stearic acid, 4 parts by weight of paraffin, and 20 parts by weight of low density polyethylene. (
Polyisobutycin 4-h as part and UV-degradable resin
-(parts) were added and mixed, and after melting and kneading, it was crushed into flakes, and this material was molded into a 5 x 1 film by injection molding.
2X 40 mrn ceramic composition; 1 body. Next, as a degreasing step for this ceramic molded body, it was irradiated with ultraviolet rays in the wavelength range of 600 to 4 Q nm for 10 minutes. The intensity of this ultraviolet ray was 20111"w/A・rji. After 7 days, the degreasing treatment by heating was carried out to 1 J. is 200℃-2Hr-250℃-
41-I r-350°C-4Hr-500°C-4Hr. The Cera E Tsuk molded body thus degreased was sintered at 1700'C-12Hr to obtain Ceramic D'.

このも67曲げ強度をイ則定したところ、62 ノ9y
’;gm’であつtこ、。
When this 67 bending strength was defined as A, it was 62 no 9y.
It's ';gm'.

実狗飽]1において、砦外線崩壊型樹脂として、ポリプ
ロピレンのかわりにポリプロピレン4重量部とを添加混
合し、溶融混練りした後、粉砕してフレーク状とし、こ
のものを射出成形機にて5×12 X 402I〃lの
セラミック成形体を1!]た。次にこのセラミック(成
形体の脱脂工程として、5秒間の電」′線照射を行ない
10 Mradの線量を与え、しかる(りに実施例1 
と同じ条件で加熱による脱脂処理をt」なった。;j)
3脂後のセラミック成形体にはフクレ、キレツ等の問題
は生じなかった。
In 1, instead of polypropylene, 4 parts by weight of polypropylene was added and mixed as a fort external line collapsible resin, melted and kneaded, and then crushed into flakes. 1 x 12 x 402I〃l ceramic molded body! ]Ta. Next, as a degreasing process for this ceramic (molded body), irradiation with electric radiation was performed for 5 seconds to give a dose of 10 Mrad (as in Example 1).
Degreasing treatment by heating was carried out under the same conditions as above. ;j)
No problems such as blistering or cracking occurred in the ceramic molded product after the third coating.

Cつ  発明の効果 本発明の実施例によれば、従来の単に加熱処理だけを行
なう脱脂l’、 f’I“に比へて極めて短時間で脱脂
処理を行なうことが出来る。しかも脱脂によるフクレ、
キレツ′Sを生じさせずに安定してセラミック成形体の
脱脂処理を行なうことが可能となつア、。      
        不U里人弁J甲士上イ欠祈司417−
C. Effects of the Invention According to the embodiments of the present invention, degreasing can be carried out in an extremely short time compared to conventional degreasing l', f'I'' which merely performs heat treatment. ,
It becomes possible to stably degrease a ceramic molded body without causing cracks.
Fuu Satonoben J Koshijou I Kashikushi 417-

Claims (1)

【特許請求の範囲】 有することを特徴とするセラミック成形用組成物。 イソブチレン、ポリメタクリレートあるいはポリα−メ
チルスチレン樹脂を含有することを特徴とするセラミッ
ク成形用組成物。 (6)成形体から有機バインダーを除去する脱脂工尤 [“1:において、成形品に槃外線あるいは電子線を照
射してこれによって反応する有(幾成分を分解せしめ、
しかる後に加熱手段によって残余の有機成分を除去する
りtを特徴とするセラミック成形組成物の11)a脂方
法。
[Claims] A ceramic molding composition characterized by comprising: A ceramic molding composition characterized by containing isobutylene, polymethacrylate or polyα-methylstyrene resin. (6) Degreasing process to remove the organic binder from the molded product [In step 1, the molded product is irradiated with a beam or electron beam and reacts with it (decomposes some components,
11) A method for preparing a ceramic molding composition, which comprises: thereafter removing residual organic components by heating means.
JP58075377A 1983-04-27 1983-04-27 Ceramic forming composition and dewaxing process Pending JPS59199570A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58075377A JPS59199570A (en) 1983-04-27 1983-04-27 Ceramic forming composition and dewaxing process

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58075377A JPS59199570A (en) 1983-04-27 1983-04-27 Ceramic forming composition and dewaxing process

Publications (1)

Publication Number Publication Date
JPS59199570A true JPS59199570A (en) 1984-11-12

Family

ID=13574445

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58075377A Pending JPS59199570A (en) 1983-04-27 1983-04-27 Ceramic forming composition and dewaxing process

Country Status (1)

Country Link
JP (1) JPS59199570A (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH01183456A (en) * 1988-01-13 1989-07-21 Shinko Electric Ind Co Ltd Formation of ceramic green sheet and via hole
JPH02275748A (en) * 1989-04-14 1990-11-09 Citizen Watch Co Ltd Molding method for powder injection-molding component
US5314850A (en) * 1985-10-31 1994-05-24 Kyocera Corporation Aluminum nitride sintered body and production thereof

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5314850A (en) * 1985-10-31 1994-05-24 Kyocera Corporation Aluminum nitride sintered body and production thereof
JPH01183456A (en) * 1988-01-13 1989-07-21 Shinko Electric Ind Co Ltd Formation of ceramic green sheet and via hole
JPH02275748A (en) * 1989-04-14 1990-11-09 Citizen Watch Co Ltd Molding method for powder injection-molding component

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