JPH0229416B2 - - Google Patents

Info

Publication number
JPH0229416B2
JPH0229416B2 JP60121581A JP12158185A JPH0229416B2 JP H0229416 B2 JPH0229416 B2 JP H0229416B2 JP 60121581 A JP60121581 A JP 60121581A JP 12158185 A JP12158185 A JP 12158185A JP H0229416 B2 JPH0229416 B2 JP H0229416B2
Authority
JP
Japan
Prior art keywords
mold
strength
alumina
slurry
minutes
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 - Lifetime
Application number
JP60121581A
Other languages
Japanese (ja)
Other versions
JPS61279335A (en
Inventor
Kazuhiro Matsuno
Toshimitsu Hori
Kazuo Sezaki
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.)
IHI Corp
Original Assignee
Ishikawajima Harima Heavy Industries 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 Ishikawajima Harima Heavy Industries Co Ltd filed Critical Ishikawajima Harima Heavy Industries Co Ltd
Priority to JP60121581A priority Critical patent/JPS61279335A/en
Publication of JPS61279335A publication Critical patent/JPS61279335A/en
Publication of JPH0229416B2 publication Critical patent/JPH0229416B2/ja
Granted legal-status Critical Current

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  • Mold Materials And Core Materials (AREA)
  • 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) この発明は精密鋳造用鋳型の製作方法に係り、
さらに詳しくいえば改良されたスラリーを使用し
て熱間強度の大きな鋳型を製作する方法に係る。 (従来技術) 例えば熱制御一方向凝固或いは単結晶精密鋳造
品を鋳型する場合、鋳型は溶融金属を注入する前
におよそ金属の融点以上の温度例えば1500℃前後
に加熱して約10分間保持したのち溶融金属を注入
し、鋳型の外側から鋳型を介して熱制御しながら
徐冷するのが通例である。 この熱制御を容易にするためには鋳型は熱伝導
率が良いか、または鋳型の肉厚が薄いものが望ま
しい。しかしながら鋳型材料として用いられる耐
火材料のアルミナは熱伝導が小さく、また肉厚を
薄くすると鋳型の強度が低下して破損し易く、湯
漏れ等の事故を起こし易いので肉厚を余り薄くで
きず、経験上肉厚は少なくとも8〜10mmとしてお
り、この点からも冷却時の熱制御が難しくなる。 (発明が解決しようとする問題点) 一般に鋳型材料として使用されるアルミナで製
作した鋳型の抗折強度(以下単に強度という)は
その組成にもよるが鑞模型を溶融して除去するい
わゆる脱鑞前の生型で30〜50Kg/cm2であり、加熱
すると約1100℃で300〜400Kg/cm2となつて最大に
なる。しかしながら更に加熱して1200℃以上にな
ると熱間の強度は急激に低下し、例えば単結晶鋳
造品の鋳造の場合の予熱温度の1500℃に10分間保
持すると約25〜30Kg/cm2まで低下する。 従つて鋳型の熱間強度がかなり小さい状態で溶
融金属を注入することになり、鋳型の肉厚を薄く
することができなかつた。 本発明はこのような事情に鑑み、熱間強度の大
きな精密鋳造用鋳型の製作方法を提供することを
目的とする。 (問題点を解決するための手段) 鑞型にスラリーと耐火物粒とを被覆してシエル
を形成する精密鋳造用鋳型の製作方法において、
アルミナ粉末とその0.1〜4重量%の二三酸化鉄
粉とをコロイダルシリカに懸濁したスラリーを使
用することを特徴とする熱間強度の大きな精密鋳
造用鋳型の製作方法に係る。 ところで、アルミナ鋳型の熱間強度低下の理由
は明らかではなく、アルミナに不純物として含ま
れるNa2Oやコロイダルシリカの安定剤である
Na2O或いはアルミナと結合材のシリカとの固相
反応による局部的なガラス相または液相の生成な
どが関与していると言われている。 しかしながら発明者の研究によればNa2Oと
1500℃の鋳型の強度との間には有意な関係は認め
られなかつた。一方、アルミナとコロイダルシリ
カとの固相反応をX線回折によつて調査した結
果、1300℃未満ではシリカが非晶質であるためα
アルミナしか同定できなかつたが、130℃ではシ
リカがクリストバライトに変態し、1500℃で1時
間以上加熱するとムライトが生成することが判つ
た。 そこでコロイダルシリカで結合したアルミナ鋳
型を1500℃で1時間加熱して熱間強度を測定した
ところ約200Kg/cm2で、著しい強度の増加が認め
られたが、同様な試料を1500℃で10分間加熱した
場合にはX線回折で同定できるほどの量のムライ
トの生成は認められず、強度も約30Kg/cm2であつ
た。 即ちコロイダルシリカで結合したアルミナ鋳型
は高温で十分な時間をかけて反応焼結させればム
ライトが生成し、鋳型の熱間強度を改善すること
ができる。 これを短時間で達成させることができれば実用
上有益であるので、これを可能にする条件を求め
るため種々実験を重ねた結果、アルミナとシリカ
との固相反応の促進には鉱化剤として二三酸化鉄
の添加が有効であることがX線回折による同定で
確認された。すなわち前記したようにアルミナと
コロイダルシリカによるムライトの生成には1500
℃およそ1時間加熱することが必要であるが、こ
れに二三酸化鉄を加えると1500℃で約10分間の加
熱でムライトが生成する。 次に実施例について説明する。 実施例 1 鑞型(70×150×7mm)の両面にゴム板(70×
150×2mm)を張り付けた模型2個を準備し、そ
れぞれに第1表に示すスラリーの配合のうちスラ
リーFと100#のアルミナを用い、常法によつて
鋳型シエルの第1層を形成した。次いで一つは第
1表のスラリーA、他の一つはスラリーBを用
い、耐火物粒即ちスタツコ材はいずれもアルミナ
粒で常法によつて合計7層から成るシエルを製作
した。シエルを十分乾燥したのちゴム板から機械
的に離して幅15mm、長さ70mmに切出し、試験片と
した。
(Industrial Application Field) This invention relates to a method for manufacturing a precision casting mold,
More specifically, the present invention relates to a method of manufacturing a mold with high hot strength using the improved slurry. (Prior art) For example, when molding a heat-controlled unidirectional solidification or single crystal precision casting product, the mold is heated to a temperature above the melting point of the metal, for example around 1500°C, and held for about 10 minutes before pouring the molten metal. The molten metal is then injected and then cooled slowly while controlling the heat from outside the mold through the mold. In order to facilitate this thermal control, it is desirable that the mold has good thermal conductivity or has a thin wall. However, alumina, which is a refractory material used as a mold material, has low thermal conductivity, and if the wall thickness is made thin, the strength of the mold decreases and it is easily damaged, and accidents such as hot water leakage are likely to occur, so the wall thickness cannot be made very thin. Experience has shown that the wall thickness is at least 8 to 10 mm, which also makes it difficult to control heat during cooling. (Problem to be solved by the invention) The bending strength (hereinafter simply referred to as strength) of a mold made of alumina, which is generally used as a mold material, depends on its composition, but the so-called de-soldering process, in which the solder model is melted and removed, In the previous raw form, it is 30-50Kg/cm 2 , and when heated, it reaches a maximum of 300-400Kg/cm 2 at about 1100℃. However, when heated further to 1,200℃ or higher, the hot strength rapidly decreases.For example, when casting a single crystal cast product, if the preheating temperature of 1,500℃ is held for 10 minutes, it decreases to about 25-30Kg/ cm2. . Therefore, molten metal must be injected while the hot strength of the mold is quite low, making it impossible to reduce the wall thickness of the mold. In view of these circumstances, an object of the present invention is to provide a method for manufacturing a precision casting mold with high hot strength. (Means for solving the problem) In a method for manufacturing a precision casting mold in which a solder mold is coated with slurry and refractory particles to form a shell,
The present invention relates to a method for manufacturing a precision casting mold with high hot strength, which uses a slurry in which alumina powder and 0.1 to 4% by weight of tri-iron oxide powder are suspended in colloidal silica. By the way, the reason for the decrease in the hot strength of alumina molds is not clear, but it may be due to Na 2 O and colloidal silica stabilizers contained in alumina as impurities.
It is said that local formation of a glass phase or liquid phase due to a solid phase reaction between Na 2 O or alumina and silica as a binder is involved. However, according to the inventor's research, Na 2 O and
No significant relationship was observed with the strength of the mold at 1500°C. On the other hand, as a result of investigating the solid phase reaction between alumina and colloidal silica using X-ray diffraction, it was found that at temperatures below 1300°C, silica is amorphous, so α
Although only alumina could be identified, it was found that silica transforms into cristobalite at 130°C, and that mullite is produced when heated at 1500°C for more than 1 hour. Therefore, when we heated an alumina mold bonded with colloidal silica at 1500℃ for 1 hour and measured its hot strength, we found that it was about 200Kg/ cm2 , which was a significant increase in strength. When heated, no mullite was produced in an amount that could be identified by X-ray diffraction, and the strength was about 30 kg/cm 2 . That is, if an alumina mold bonded with colloidal silica is reacted and sintered at high temperature for a sufficient period of time, mullite will be generated and the hot strength of the mold can be improved. It would be of practical benefit if this could be achieved in a short period of time, so we conducted various experiments to find conditions that would make this possible. Identification by X-ray diffraction confirmed that the addition of iron trioxide was effective. In other words, as mentioned above, the production of mullite from alumina and colloidal silica requires 1500
It is necessary to heat the product for about 1 hour at 1500°C, but if triiron oxide is added to this, mullite is produced by heating at 1500°C for about 10 minutes. Next, an example will be described. Example 1 Rubber plates (70×
150 x 2 mm) were prepared, and using slurry F and 100# alumina from the slurry composition shown in Table 1 on each model, the first layer of the mold shell was formed by a conventional method. . Next, using slurry A shown in Table 1 for one shell and slurry B for the other shell, shells consisting of a total of seven layers were fabricated using alumina particles as refractory particles, that is, stucco materials, by a conventional method. After thoroughly drying the shell, it was mechanically separated from the rubber plate and cut into a piece of 15 mm wide and 70 mm long to be used as a test piece.

【表】 試験片の生強度は35〜45Kg/cm2、1200〜1500℃
で10分間加熱保持したときの熱間強度を第1図に
示す。なお第1図には1500℃に1時間保持したと
きの強度を対比のため示してある。 スラリーAとアルミナで製作した鋳型の強度は
1200℃の約200Kg/cm2から1500℃、10分加熱で約
25Kg/cm2に低下した。この状態ではX線回折でム
ライトは同定できなかつた。これを1500℃に1時
間加熱すると前記したようにムライトが生成さ
れ、強度も約200Kg/cm2に増加する。 一方、スラリーに鉱化剤として二三酸化鉄を添
加したスラリーBを用いて製作した鋳型は1400℃
ではスラリーAを用いたものと強度は同等であつ
たが、1500℃×10分間加熱で約150Kg/cm2に増加
し、X線回折でムライトの生成が同定された。
1500℃×1時間加熱では強度が約250Kg/cm2に上
昇した。 二三酸化鉄の添加量はアルミナ紛に対して0.1
〜4重量%が適当で、0.1%以下では1500℃×10
分間の加熱ではムライトの生成が不充分であつて
鋳型の強度の増加が期待できない。ムライトの生
成量はX線回折で同定できるおよそ5%以上が必
要であるが、ムライトの量を多くしようとして二
三酸化鉄の量を多くすると鋳型の耐火度が低下す
るので好ましくなく、従つて4%を限度とするの
が良く、好ましくは0.5〜2%とする。その粒度
はおよそ300メツシユとするのが反応性の点から
好ましい。 加熱温度は単結晶鋳造品鋳造の場合の注入温度
に近い温度の1500℃を基準とし、注入温度が高い
場合には高くするが、経済性と作業性の点からお
よそ1570℃以下とするのが良く、またおよそ1450
℃以下では満足な鋳造品を得ることが難しい。 加熱時間は10分間を基準とし、経済性と作業性
の点からおよそ5分以上、15分以下とするのが良
い。 スラリーと共に用いる耐火物粒の大きさは強度
と通気性を考慮しておよそ0.5〜1.5mmが適当であ
る。 このように、コロイダルシリカに二三酸化鉄を
所定量添加したスラリーとアルミナ紛とを使つて
鑞型模型に着せてシエルを形成し、脱鑞したのち
1500℃で10分間という短い時間加熱するだけで、
鑞型の熱間強度は従来の抗析力の約6倍の150
Kg/cm2程度となるので、従来10mm程度の肉厚が必
要であつた鋳型が4〜5mmの肉厚の鋳型としても
充分な強度を有することとなる。従つて、精密鋳
造に際して熱制御が行いやすく、方向性凝固或い
は単結晶鋳物の鋳造が容易になり、良品歩留りが
上昇し、或いはシエルのコ−テイング回数を減少
させることができる等、実用上の効果が極めて大
きい。 実施例 2 直径6mmのクリープラプチヤ試験片2本を含む
単結晶鋳造用の鑞型模型を用い、鋳型は実施例1
と同様にして6回のコーテイングで肉厚4〜5mm
の鋳型を製作し、脱鑞後1100℃で1時間焼成して
冷却した。ついで鋳型を単結晶炉に入れ、1500℃
まで40分で昇温、10分間保持したのち、通常の単
結晶鋳物鋳造条件で注入した。鋳型の破壊その他
の事故や欠陥を生ずることなく、満足な単結晶精
密鋳造品を得ることができた。 (効果) アルミナ粉末とその0.1〜4重量%の二三酸化
鉄粉とをコロイダルシリカに懸濁したスラリーを
使用し、1450〜1570℃で5〜15分間加熱するよう
にしたので、鋳型の熱間強度を高めることがで
き、その肉厚を薄くすることが可能になつて精密
鋳造の際の熱制御が行いやすくなると共に、短時
間で焼成されることで、鋳型製作上の作業性及び
経済性が良好で、極めて実際的である。
[Table] The green strength of the test piece is 35~45Kg/ cm2 , 1200~1500℃
Figure 1 shows the hot strength when heated and held for 10 minutes. For comparison, Fig. 1 shows the strength when held at 1500°C for 1 hour. The strength of the mold made with slurry A and alumina is
Approximately 200Kg/cm 2 at 1200℃ to approximately 10 minutes at 1500℃
It decreased to 25Kg/cm 2 . In this state, mullite could not be identified by X-ray diffraction. When this is heated to 1500° C. for 1 hour, mullite is produced as described above, and the strength increases to about 200 kg/cm 2 . On the other hand, the mold made using Slurry B, in which iron dioxide was added as a mineralizing agent, was heated to 1400℃.
Although the strength was the same as that using slurry A, it increased to about 150 kg/cm 2 after heating at 1500° C. for 10 minutes, and the formation of mullite was identified by X-ray diffraction.
After heating at 1500°C for 1 hour, the strength increased to approximately 250Kg/cm 2 . The amount of triferric oxide added is 0.1 per alumina powder.
~4% by weight is appropriate, and if it is less than 0.1%, the temperature is 1500℃ x 10
Heating for 1 minute will not produce enough mullite and no increase in the strength of the mold can be expected. The amount of mullite produced needs to be approximately 5% or more, which can be identified by X-ray diffraction, but increasing the amount of tri-iron oxide in an attempt to increase the amount of mullite is undesirable because the refractory of the mold will decrease. The limit is preferably 4%, preferably 0.5 to 2%. The particle size is preferably about 300 mesh from the viewpoint of reactivity. The standard heating temperature is 1500℃, which is close to the injection temperature for single-crystal casting.If the injection temperature is high, it will be higher, but from the viewpoint of economy and workability, it is recommended to keep it at about 1570℃ or less. Good, also around 1450
If the temperature is below ℃, it is difficult to obtain a satisfactory cast product. The standard heating time is 10 minutes, and from the point of view of economy and workability, it is preferable to set the heating time to about 5 minutes or more and 15 minutes or less. The appropriate size of the refractory particles used with the slurry is approximately 0.5 to 1.5 mm in consideration of strength and air permeability. In this way, a slurry made by adding a predetermined amount of iron dioxide to colloidal silica and alumina powder are applied to a solder model to form a shell, and after de-soldering,
Just by heating at 1500℃ for 10 minutes,
The hot strength of the solder mold is 150, which is about 6 times the resistance strength of conventional products.
Since it is about Kg/cm 2 , the mold, which conventionally required a wall thickness of about 10 mm, has sufficient strength even as a mold with a wall thickness of 4 to 5 mm. Therefore, it is easy to control heat during precision casting, directional solidification or casting of single crystal castings is facilitated, the yield of good products is increased, and the number of times of shell coating can be reduced. The effect is extremely large. Example 2 A chisel type model for single crystal casting containing two creep rapture test pieces with a diameter of 6 mm was used, and the mold was the same as that of Example 1.
In the same manner as above, coat the wall 6 times to obtain a wall thickness of 4-5 mm.
A mold was made, and after de-soldering, it was fired at 1100°C for 1 hour and cooled. The mold was then placed in a single crystal furnace and heated to 1500°C.
The temperature was raised in 40 minutes to 100%, held for 10 minutes, and then poured under normal single-crystal casting conditions. A satisfactory single-crystal precision cast product could be obtained without mold destruction or other accidents or defects. (Effect) We used a slurry of alumina powder and 0.1 to 4% by weight of iron dioxide powder suspended in colloidal silica, and heated it at 1450 to 1570°C for 5 to 15 minutes. It is possible to increase the mechanical strength and reduce the wall thickness, which makes it easier to control heat during precision casting, and because it is fired in a short time, it improves the workability and economy of mold production. It has good properties and is very practical.

【図面の簡単な説明】[Brief explanation of drawings]

第1図はアルミナ鋳型の加熱温度時間と熱間強
度との関係を示すグラフである。
FIG. 1 is a graph showing the relationship between heating temperature time and hot strength of an alumina mold.

Claims (1)

【特許請求の範囲】[Claims] 1 鑞型にスラリーと耐火物粒とを被覆してシエ
ルを形成する精密鋳造用鋳型の製作方法におい
て、アルミナ粉末とその0.1〜4重量%の二三酸
化鉄粉とをコロイダルシリカに懸濁したスラリー
を使用し、1450〜1570℃で5〜15分間加熱するこ
とを特徴とする熱間強度の大きな精密鋳造用アル
ミナ鋳型の製作方法。
1. In a method for manufacturing a precision casting mold in which a solder mold is coated with slurry and refractory particles to form a shell, alumina powder and 0.1 to 4% by weight of triiron dioxide powder are suspended in colloidal silica. A method for producing an alumina mold for precision casting with high hot strength, characterized by using slurry and heating at 1450 to 1570°C for 5 to 15 minutes.
JP60121581A 1985-06-06 1985-06-06 Production of alumina mold for precision casting Granted JPS61279335A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60121581A JPS61279335A (en) 1985-06-06 1985-06-06 Production of alumina mold for precision casting

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60121581A JPS61279335A (en) 1985-06-06 1985-06-06 Production of alumina mold for precision casting

Publications (2)

Publication Number Publication Date
JPS61279335A JPS61279335A (en) 1986-12-10
JPH0229416B2 true JPH0229416B2 (en) 1990-06-29

Family

ID=14814783

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60121581A Granted JPS61279335A (en) 1985-06-06 1985-06-06 Production of alumina mold for precision casting

Country Status (1)

Country Link
JP (1) JPS61279335A (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS59197338A (en) * 1983-04-21 1984-11-08 Agency Of Ind Science & Technol Production of mold for precision casting

Also Published As

Publication number Publication date
JPS61279335A (en) 1986-12-10

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