JPH038533A - Rare earth oxide slurry - Google Patents

Rare earth oxide slurry

Info

Publication number
JPH038533A
JPH038533A JP3552690A JP3552690A JPH038533A JP H038533 A JPH038533 A JP H038533A JP 3552690 A JP3552690 A JP 3552690A JP 3552690 A JP3552690 A JP 3552690A JP H038533 A JPH038533 A JP H038533A
Authority
JP
Japan
Prior art keywords
slurry
rare earth
casting
wax
earth oxide
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
JP3552690A
Other languages
Japanese (ja)
Inventor
Yuji Kimura
裕司 木村
Akifumi Yoshida
吉田 紀史
Koji Nishikawa
浩二 西川
Kenichiro Suzuki
健一郎 鈴木
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.)
JFE Steel Corp
Shin Etsu Chemical Co Ltd
Original Assignee
Shin Etsu Chemical Co Ltd
Kawasaki Steel Corp
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 Shin Etsu Chemical Co Ltd, Kawasaki Steel Corp filed Critical Shin Etsu Chemical Co Ltd
Priority to JP3552690A priority Critical patent/JPH038533A/en
Publication of JPH038533A publication Critical patent/JPH038533A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To produce a casting having good dimensional accuracy by alternately applying a slurry contg. a rare earth oxide and water soluble polycarboxylic acid and granular ceramics on the surface of a lost wax pattern and drying the coatings at the time of casting a high melting active metal, such as Ti, by a lost wax method. CONSTITUTION:The slurry consisting of the aq. soln. contg. 0.1 to 2.5 pts.wt. alginate, such as sodium alginate per 100 pts.wt. oxide of the rare earth element having the grain size distribution of 30 to 100wt.%<=2mum is applied on the surface of the wax pattern having the same shape and size as the shape and size of the casting and the powder of the ceramics consisting of the oxide of the rare earth element used to the above-mentioned slurry is stuck thereon at the time of casting the metal, such as Ti or Ti alloy, having the high melting temp. and high activity by the lost wax casting method. Refractory coating layers are formed on the surface of the wax pattern by repeating this operation >=1 times and thereafter, the wax is melted away and the Ti, etc., are cast into the formed hole. The Ti casting which has no brittle reaction cured layers on the surface and has the high dimensional accuracy is thus produced.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は希土類酸化物を主剤とするチタンあるいはチタ
ン合金等の高融点活性金属の鋳造に用いるロストワック
ス鋳型用スラリー組成物に関するものである。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a slurry composition for lost wax casting molds, which is used for casting high melting point active metals such as titanium or titanium alloys, which has a rare earth oxide as a main ingredient.

(従来の技術) 希土類酸化物はセラミックス原料としてその特性を利用
して顔料、釉薬、ガラス、耐火ルツボ等に用途が拡大し
ている。ロストワックス鋳造法の鋳型の表面被覆剤(特
開昭63−115644 参照)として非水系のイツト
リア(y、o、)スラリーが用いられているが、これは
例えば、エチルシリケート加水分解液をバインダーとし
て鋳型を製造した場合、 SiO□分がチタンあるいは
チタン合金等の高融点活性金属を鋳造した際にこれらと
反応して、鋳造体表面に硬(て脆い反応硬化層を生じ、
これを除去するためケミカルミーリング等の研削、研磨
等を施すので高い寸法精度が得られず、また、非水系の
プロピレングリコール、エチルエーテルを使用するため
防爆対策や作業衛生環境対策に多大の費用を要する等の
欠点があった。
(Prior Art) Rare earth oxides are used as raw materials for ceramics, and their properties are being utilized to expand their use in pigments, glazes, glasses, refractory crucibles, and the like. A non-aqueous ittria (y, o,) slurry is used as a surface coating agent for a mold in the lost wax casting method (see JP-A-63-115644). When manufacturing molds, SiO□ reacts with high melting point active metals such as titanium or titanium alloys when they are cast, creating a hard (and brittle) reaction hardening layer on the surface of the cast body.
In order to remove this, grinding and polishing such as chemical milling is required, making it impossible to obtain high dimensional accuracy.Also, since non-aqueous propylene glycol and ethyl ether are used, a large amount of cost is required for explosion-proof measures and work hygiene environment measures. There were some drawbacks, such as the need for

(発明が解決しようとする課題) 本発明は前述した不利、欠点を解決することを技術的課
題とするもので、鋳造体表面に硬化層のない、寸法精度
の高いロストワックス鋳造品を得るための鋳型用希土類
酸化物スラリーを提供することにある。
(Problems to be Solved by the Invention) The technical object of the present invention is to solve the above-mentioned disadvantages and drawbacks, and to obtain a lost wax cast product with high dimensional accuracy and no hardened layer on the surface of the cast product. An object of the present invention is to provide a rare earth oxide slurry for molding.

(課題を解決するための手段) 本発明者等はかかる課題を解決するために希土類酸化物
の粒度分布、スラリー濃度、水溶性ポリカルボン酸塩と
添加量、水溶液濃度等鋳型被覆層の特性に関与する因子
について検討を重ねた結果、本発明を完成するに到った
(Means for Solving the Problem) In order to solve the problem, the present inventors have investigated the characteristics of the mold coating layer, such as the particle size distribution of the rare earth oxide, the slurry concentration, the amount of water-soluble polycarboxylate added, and the concentration of the aqueous solution. As a result of repeated studies on the factors involved, the present invention has been completed.

本発明の要旨は、 希土類酸化物100重量部に対し、水溶性ポリカルボン
酸塩0,1〜2.5重量部を含む水溶液を添加して成る
希土類酸化物スラリーにある。
The gist of the present invention resides in a rare earth oxide slurry made by adding an aqueous solution containing 0.1 to 2.5 parts by weight of a water-soluble polycarboxylate to 100 parts by weight of the rare earth oxide.

以下、本発明の詳細な説明する。The present invention will be explained in detail below.

先づ、本発明の対象となるスラリー用希土類酸化物はL
a、 Ce、Pr、Nd、Sm、Eu、Gd、Tb、D
y、Ha、Er、Tm、 Yb、 Lu等の他、Yある
いはScの酸化物から選択される1種または2種以上の
混合物に適応される。
First, the rare earth oxide for slurry that is the object of the present invention is L
a, Ce, Pr, Nd, Sm, Eu, Gd, Tb, D
In addition to oxides of Y, Ha, Er, Tm, Yb, Lu, etc., the present invention is applicable to one type or a mixture of two or more types selected from oxides of Y or Sc.

これら酸化物の粒度分布は2 jt m以下の粒子が3
0〜100重量%(以下wt%とする)のものが良(、
さらに好ましくは、2μm以下が50〜90wt%、2
〜5μmが0〜40wt%、および5μm以上が10〜
50wt%である。2μm以下の微粒子が30wt%未
満で、5μm以上が50wt%以上になると焼成後の被
覆層の強度が弱く、剥げ落ち易くなる。希土類酸化物の
スラリー濃度は40〜80wt%が良く、好ましくは5
5〜65wt%である。40wt%以下では乾燥時にク
ラックを生じ易く、80wt%以上ではスラリーの粘度
が高過ぎて、所望の厚さの被覆Mを構成することが困難
となる。
The particle size distribution of these oxides is such that particles of 2 jt m or less are 3
0 to 100% by weight (hereinafter referred to as wt%) is good (,
More preferably, 50 to 90 wt%, 2 μm or less
~5μm is 0~40wt%, and 5μm or more is 10~
It is 50wt%. If the amount of fine particles of 2 μm or less is less than 30 wt% and the amount of fine particles of 5 μm or more is 50 wt% or more, the strength of the coating layer after firing will be weak and it will easily peel off. The slurry concentration of rare earth oxide is preferably 40 to 80 wt%, preferably 5
It is 5 to 65 wt%. If it is less than 40 wt%, cracks will easily occur during drying, and if it is more than 80 wt%, the viscosity of the slurry will be too high, making it difficult to form a coating M with a desired thickness.

次に本発明の最大の特徴である希土類酸化物スラリーの
安定性を保持し、酸化物微粒子の分散性を高め、被覆層
乾燥時のグリーン強度を維持するために水溶性ポリカル
ボン酸塩を添加するが、本発明では、アルギン酸ソーダ
(以下SAAとする)、アルギン酸アンモニウム(以下
AAAとする)、アルギン酸アミン、ポリアクリル酸ソ
ーダ(以下5PAAとする)、ポリアクリル酸アンモニ
ウムから選択される1種または2種以上から成る混合物
がよく、中でもアルギン酸塩が好適に使用される。その
水溶液濃度は0.1〜5wt%がよく、さらに好ましく
は0.5〜2wt%である。  0.1wt%以下では
バインダー効果がなく、5wt%以上ではスラリーが高
粘度となり所望の被で層の厚さにならない。希土類酸化
物に対する添加】は酸化物100重量部に対しく1.1
〜2.5重量部がよく、好ましくは03〜1.0重量部
である。0.1重量部以下では乾燥時にクラックを生じ
易く、2.5重量部以上ではスラリーの粘度が高過ぎて
成形不能となる。
Next, water-soluble polycarboxylate is added to maintain the stability of the rare earth oxide slurry, which is the most important feature of the present invention, to increase the dispersibility of the oxide fine particles, and to maintain the green strength when the coating layer dries. However, in the present invention, one selected from sodium alginate (hereinafter referred to as SAA), ammonium alginate (hereinafter referred to as AAA), amine alginate, sodium polyacrylate (hereinafter referred to as 5PAA), or ammonium polyacrylate. A mixture of two or more types is preferable, and among them, alginates are preferably used. The concentration of the aqueous solution is preferably 0.1 to 5 wt%, more preferably 0.5 to 2 wt%. If it is less than 0.1 wt%, there will be no binder effect, and if it is more than 5 wt%, the slurry will have a high viscosity and will not have the desired layer thickness. Addition to rare earth oxide] is 1.1 per 100 parts by weight of oxide.
-2.5 parts by weight is good, preferably 03-1.0 parts by weight. If it is less than 0.1 part by weight, cracks are likely to occur during drying, and if it is more than 2.5 parts by weight, the viscosity of the slurry is too high and it becomes impossible to mold.

この希土類酸化物スラリーの製法は常法に従えばよ(、
先づ水溶性ポリカルボン酸塩水溶液を未溶解分のない所
望の濃度に溶解調整し、これを撹拌しつつ粒度調整した
希土類酸化物微粉末を少量づつ添加し所定1度のスラリ
ーとする。次いでこのスラリーをボールミル、自動乳鉢
等に仕込み、未分散粒子が消滅するまで充分混練しスラ
リーを製造する。脱水成形体に気泡の混入を防止するた
め、必要に応じ消泡剤を添加することが好ましく、シリ
コーン系、POE−POP縮合縮合環系用いられる。添
加量としては、希土類酸化物100重量部に対し、0.
O1〜1.0重量部が好ましい。
This rare earth oxide slurry can be produced according to the conventional method (
First, a water-soluble polycarboxylate aqueous solution is dissolved and adjusted to a desired concentration without any undissolved matter, and while stirring, rare earth oxide fine powder whose particle size has been adjusted is added little by little to form a predetermined slurry. Next, this slurry is charged into a ball mill, an automatic mortar, etc., and sufficiently kneaded until undispersed particles disappear to produce a slurry. In order to prevent air bubbles from being mixed into the dehydrated molded product, it is preferable to add an antifoaming agent if necessary, and a silicone type or a POE-POP condensed ring type is used. The amount added is 0.00 parts by weight per 100 parts by weight of the rare earth oxide.
1 to 1.0 parts by weight of O is preferred.

次に上記スラリーを用いたロストワックス鋳造法による
高融点活性金属鋳造品の製造方法について詳述する。
Next, a method for manufacturing a high melting point active metal casting by a lost wax casting method using the above slurry will be described in detail.

■目的とする鋳造品と同形状のワックス模型を1個以上
準備し、これをワックス製の湯口、湯道に接着し、所謂
ツリーとする。
■Prepare one or more wax models of the same shape as the desired cast product, and glue them to wax sprues and runners to form a so-called tree.

■上記ツリーを前記水溶性ポリカルボン酸塩含有希土類
酸化物スラリーに浸漬し、ワックス表面をスラリーにて
被覆する。
(2) The tree is immersed in the water-soluble polycarboxylate-containing rare earth oxide slurry, and the wax surface is coated with the slurry.

■ワックス表面のスラリーが乾(前に、スラリー被覆層
の上からセラミック粒状物(以下スタッコという)を万
遍なく付着させる。ここで用いるスタッコは耐火度の高
い耐火材であればその種類を問わないが、スラリーに使
用した希土類酸化物が好ましい。
■ Once the slurry on the wax surface dries, apply ceramic granules (hereinafter referred to as stucco) evenly over the slurry coating layer. However, rare earth oxides used in the slurry are preferred.

■上記■および■の工程を1回以上繰返す。■Repeat the steps of ■ and ■ above one or more times.

■その後は、従来から実施されている公知の方法に基づ
き、コロイダルシリカあるいはエチルシリケート加水分
解液及びジルコン粉末あるいは溶融シリカ粉末等のセラ
ミック微粉から成るスラリーに浸漬した後、ムライト質
あるいはジルコン等のセラミックで被覆するという操作
を被覆層の厚さが所定の厚さになるまで繰返す。
■After that, based on the conventionally known method, after immersing in a slurry consisting of colloidal silica or ethyl silicate hydrolyzed solution and ceramic fine powder such as zircon powder or fused silica powder, The operation of coating with is repeated until the thickness of the coating layer reaches a predetermined thickness.

■被覆層が充分に乾燥した後ワックスを溶出し、残った
鋳型を焼成する。
■After the coating layer has sufficiently dried, the wax is eluted and the remaining mold is fired.

■チタンあるいはチタン合金等の高融点活性金属を溶解
し、前記鋳型に注湯する。これら金属の溶解方法は問わ
ないが、真空あるいは非酸化性雰囲気中での溶解が望ま
しい。
(2) A high melting point active metal such as titanium or titanium alloy is melted and poured into the mold. The method of melting these metals is not critical, but melting in a vacuum or in a non-oxidizing atmosphere is preferable.

■鋳型内で金属が凝固、冷却した後、鋳型を除去して鋳
造品を取出し、湯道、湯口等を除去して製品とする。
■After the metal solidifies and cools in the mold, the mold is removed to take out the cast product, and the runners, sprues, etc. are removed to make the product.

以下本発明をロストワックス鋳造用鋳型の表面被覆剤に
適応した実施例を挙げて具体的に説明するが、本発明は
これら実施例に限定されるものではない。例中、部およ
び%はすべで重量基準である。
The present invention will be specifically described below with reference to examples in which it is applied to a surface coating agent for lost wax casting molds, but the present invention is not limited to these examples. In the examples, all parts and percentages are by weight.

始めに、鋳型の性状について述べる。First, the properties of the mold will be described.

(実施例1) 1、スラリーの調整 アルギン酸アンモニウム(AAA)2部に水198部を
加えて1wt%水溶液とし、これに消泡剤として、プル
ロニックL−61(サンノブコ社製商品名)を加えて完
全に溶解した。次にボールミルにイツトリア(Y、O,
)  100部を仕込み、これに上記水溶液55部を添
加し40分間混練しスラリーを調整した。イツトリアの
粒度分布は第2表I−Aのものを使用した。
(Example 1) 1. Preparation of slurry Add 198 parts of water to 2 parts of ammonium alginate (AAA) to make a 1 wt% aqueous solution, and add Pluronic L-61 (trade name, manufactured by San Nobuco Co., Ltd.) as an antifoaming agent to this. Completely dissolved. Next, ittria (Y, O,
) to which 55 parts of the above aqueous solution was added and kneaded for 40 minutes to prepare a slurry. The particle size distribution of Ittria was as shown in Table 2 I-A.

2、ロストワックス法鋳造鋳型の製作 ■目的とする鋳物の形をしたワックス製の型を準備し、
上記スラリーにこの型を浸漬し、ワックス表面をスラリ
ーで被覆する。
2. Production of lost wax casting mold■ Prepare a wax mold in the shape of the desired casting,
The mold is immersed in the slurry to coat the wax surface with the slurry.

■ワックス表面のスラリーが乾(前に、スラリー被覆層
の上からイツトリアスタッコを互選なく付着させる。
■The slurry on the wax surface dries (first, apply ittria stucco on top of the slurry coating layer without any overlap).

■第2層以降は従来から実施されている公知の方法にも
とづき、コロイダルシリカ及びジルコン粉末から成るス
ラリーに浸漬した後、ムライト質耐火物のスタッコ被覆
という操作を被覆層の厚さが所定の厚さになるまで繰り
返す。
■The second layer and subsequent layers are coated with stucco using mullite refractories after being immersed in a slurry made of colloidal silica and zircon powder, based on a conventionally known method. Repeat until it is.

■被覆層が十分に乾燥した後ワックスを溶出し、残った
鋳型を焼成する。
■After the coating layer has sufficiently dried, the wax is eluted and the remaining mold is fired.

次いで、作製した鋳型の表面被覆層(イツトリアスラリ
ーおよびイツトリアスタッコ層)の厚さ約1mmの外観
および断面を観察し評価した。被覆属表面にクラックは
全(な(、また、被覆層の断面に気泡は存在しなかった
。このスラリー組成と鋳型の表面被覆層の外観評価結果
を第1表に示した。
Next, the appearance and cross section of the surface coating layer (Yutria slurry and Yetria stucco layer) of about 1 mm in thickness of the produced mold were observed and evaluated. There were no cracks on the surface of the coating, and no bubbles were present in the cross section of the coating layer. Table 1 shows the composition of this slurry and the results of evaluating the appearance of the surface coating layer of the mold.

(実施例2、比較例1.2) 実施例2は消泡剤を無添加とした以外は実施例1と同様
に実施し、比較例1はAAAの対イツトノア添加量が少
ない場合、比較例2は多い場合でスラリー組成と鋳型の
表面被覆層の評価結果を第1表に示した。
(Example 2, Comparative Example 1.2) Example 2 was carried out in the same manner as Example 1 except that no antifoaming agent was added. Table 1 shows the slurry composition and the evaluation results of the surface coating layer of the mold.

(実施例3.4) 実施例3.4はイツトリアの粒度分布が第2表のI−B
、I−Cのものを使用した以外は実施例1と同様に実施
し、スラリー組成と鋳型の表面被覆層の評価結果を第1
表に示した。
(Example 3.4) In Example 3.4, the particle size distribution of Ittria was I-B in Table 2.
, I-C was used in the same manner as in Example 1, and the evaluation results of the slurry composition and the surface coating layer of the mold were
Shown in the table.

(実施例5.6) 実施例5.6は希土類酸化物を夫々セリウム酸化物、エ
ルビウム酸化物に変えた以外は実施例1と同様に実施し
、その条件と結果を第1表に示す。また、希土類酸化物
の粒度分布を第2表に示す。
(Example 5.6) Examples 5 and 6 were carried out in the same manner as in Example 1 except that the rare earth oxides were changed to cerium oxide and erbium oxide, respectively, and the conditions and results are shown in Table 1. Furthermore, the particle size distribution of the rare earth oxides is shown in Table 2.

(比較例3.4) 比較例3.4はイツトリアのスラリー濃度と水溶性ポリ
カルボン酸塩の対イツトリア添加量を変化させた以外は
実施例1と同様に実施し、その条件と結果を第1表に示
した。
(Comparative Example 3.4) Comparative Example 3.4 was carried out in the same manner as Example 1, except that the slurry concentration of yttria and the amount of water-soluble polycarboxylate added to yttria were changed, and the conditions and results were It is shown in Table 1.

(実施例7.8) 実施例7.8はバインダーとしての水溶性ポリカルボン
酸塩を夫々SAA、5PAAに変え、これらバインダー
の水溶液濃度、対イツトリア添加量を変化させた以外は
実施例1と同様に実施し、その条件と結果を第1表に示
す。
(Example 7.8) Example 7.8 is the same as Example 1 except that the water-soluble polycarboxylate as the binder was changed to SAA and 5PAA, respectively, and the aqueous solution concentration of these binders and the amount added to itria were changed. The same procedure was carried out, and the conditions and results are shown in Table 1.

次に、上記実施例に示した鋳型にチタン合金を鋳造した
際の条件と結果を述べる。
Next, the conditions and results when titanium alloy was cast into the mold shown in the above example will be described.

(実施例9.10、比較例5.6) 実施例9.10として実施例1.8で作製した鋳型並び
に比較例5.6として第3表に示すスラリーおよびスタ
ッコを第1層とし、以後、実施例1と同一条件で作製し
た鋳型を1個の湯口を共有する1連の鋳型に組み合わせ
た。電子ビーム溶解炉にアルミニウム6%、バナジウム
4%を含むチタン合金を溶解し、前記鋳型内に遠心鋳造
した。
(Example 9.10, Comparative Example 5.6) The mold prepared in Example 1.8 as Example 9.10 and the slurry and stucco shown in Table 3 as Comparative Example 5.6 were used as the first layer, and thereafter The molds produced under the same conditions as in Example 1 were combined into a series of molds sharing one sprue. A titanium alloy containing 6% aluminum and 4% vanadium was melted in an electron beam melting furnace and centrifugally cast into the mold.

チタン合金が凝固、冷却後鋳型を除去し、サンドブラス
ト仕上した後、表面硬化層深さおよび表面粗さを測定し
た。その結果を第3表に示す。
After the titanium alloy had solidified and cooled, the mold was removed and the hardened surface layer depth and surface roughness were measured after sandblasting. The results are shown in Table 3.

(発明の効果) 本発明の水溶性ポリカルボン酸塩を配合した希土類酸化
物スラリーは、ロストワックス鋳造用鋳型の表面被覆剤
用スラリーとして使用した場合に好適であり、鋳型表面
に肌荒れがな(、寸法精度が高く、気泡、空隙のない精
密な鋳造品を作製可第 2 表 能で産業上極めて利用価値の高いものである。
(Effects of the Invention) The rare earth oxide slurry blended with the water-soluble polycarboxylate of the present invention is suitable when used as a slurry for a surface coating agent of a lost wax casting mold, and does not cause roughness on the surface of the mold. It has high dimensional accuracy and can produce precision cast products without bubbles or voids, making it extremely useful in industry.

Claims (1)

【特許請求の範囲】 1、希土類酸化物100重量部に対し、水溶性ポリカル
ボン酸塩0.1〜2.5重量部を含む水溶液を添加して
成る希土類酸化物スラリー。 2、所定形状を有するワックス模型に耐火物粉末のスラ
リーを塗布した後、セラミックス粒状物を散布する工程
を1回以上繰返して、該模型に耐火物による被覆層を形
成し乾燥する工程と、該模型からワックスを溶出し焼成
する工程を経て鋳型を作製し、該鋳型に金属融液を注入
して成形品を得る高融点活性金属成形品の製造法におい
て、該スラリーとして請求項1に記載の希土類酸化物ス
ラリーを用いることを特徴とする表面性状の優れた高融
点活性金属成形品の製造方法。
[Claims] 1. A rare earth oxide slurry obtained by adding an aqueous solution containing 0.1 to 2.5 parts by weight of a water-soluble polycarboxylate to 100 parts by weight of the rare earth oxide. 2. After applying a refractory powder slurry to a wax model having a predetermined shape, repeating the step of scattering ceramic granules one or more times to form a refractory coating layer on the model and drying it; In a method for manufacturing a high melting point active metal molded article, in which a mold is prepared through a step of eluting wax from a model and firing it, and a molded product is obtained by injecting a metal melt into the mold, the slurry is the slurry according to claim 1. A method for producing a high melting point active metal molded article with excellent surface properties, characterized by using a rare earth oxide slurry.
JP3552690A 1989-03-22 1990-02-16 Rare earth oxide slurry Pending JPH038533A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP3552690A JPH038533A (en) 1989-03-22 1990-02-16 Rare earth oxide slurry

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP1-70191 1989-03-22
JP7019189 1989-03-22
JP3552690A JPH038533A (en) 1989-03-22 1990-02-16 Rare earth oxide slurry

Publications (1)

Publication Number Publication Date
JPH038533A true JPH038533A (en) 1991-01-16

Family

ID=26374525

Family Applications (1)

Application Number Title Priority Date Filing Date
JP3552690A Pending JPH038533A (en) 1989-03-22 1990-02-16 Rare earth oxide slurry

Country Status (1)

Country Link
JP (1) JPH038533A (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1999030854A1 (en) * 1997-12-15 1999-06-24 Pcc Structurals, Inc. Method for imaging inclusions in investment castings
US6237671B1 (en) 1997-10-30 2001-05-29 Howmet Research Corporation Method of casting with improved detectability of subsurface inclusions
JP2003081241A (en) * 2001-09-14 2003-03-19 Daiwa Can Co Ltd Drawn-formed can made of aluminum and its manufacturing method
US6619368B1 (en) 1997-12-15 2003-09-16 Pcc Structurals, Inc. Method for imaging inclusions in investment castings
CN105397026A (en) * 2015-11-30 2016-03-16 贵州安吉航空精密铸造有限责任公司 Casting process for forming complex pipeline in titanium alloy investment casting

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6237671B1 (en) 1997-10-30 2001-05-29 Howmet Research Corporation Method of casting with improved detectability of subsurface inclusions
WO1999030854A1 (en) * 1997-12-15 1999-06-24 Pcc Structurals, Inc. Method for imaging inclusions in investment castings
US6102099A (en) * 1997-12-15 2000-08-15 Pcc Structurals, Inc. Method for imaging inclusions in investment castings
US6619368B1 (en) 1997-12-15 2003-09-16 Pcc Structurals, Inc. Method for imaging inclusions in investment castings
JP2003081241A (en) * 2001-09-14 2003-03-19 Daiwa Can Co Ltd Drawn-formed can made of aluminum and its manufacturing method
CN105397026A (en) * 2015-11-30 2016-03-16 贵州安吉航空精密铸造有限责任公司 Casting process for forming complex pipeline in titanium alloy investment casting

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