JPS60221501A - Production of sintered metallic body - Google Patents
Production of sintered metallic bodyInfo
- Publication number
- JPS60221501A JPS60221501A JP59077117A JP7711784A JPS60221501A JP S60221501 A JPS60221501 A JP S60221501A JP 59077117 A JP59077117 A JP 59077117A JP 7711784 A JP7711784 A JP 7711784A JP S60221501 A JPS60221501 A JP S60221501A
- Authority
- JP
- Japan
- Prior art keywords
- molding
- heated
- binder
- powder
- plastic material
- 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
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22F—WORKING METALLIC POWDER; MANUFACTURE OF ARTICLES FROM METALLIC POWDER; MAKING METALLIC POWDER; APPARATUS OR DEVICES SPECIALLY ADAPTED FOR METALLIC POWDER
- B22F3/00—Manufacture of workpieces or articles from metallic powder characterised by the manner of compacting or sintering; Apparatus specially adapted therefor ; Presses and furnaces
- B22F3/12—Both compacting and sintering
Landscapes
- Engineering & Computer Science (AREA)
- Manufacturing & Machinery (AREA)
- Mechanical Engineering (AREA)
- Powder Metallurgy (AREA)
Abstract
Description
【発明の詳細な説明】 A0発明の目的 (11産業上の利用分野 本発明は金属焼結体の製造方法に関する。[Detailed description of the invention] A0 Purpose of invention (11 industrial application fields The present invention relates to a method for manufacturing a metal sintered body.
(2)従来の技術
金属焼結体を製造する場合、その成形作業を容易に行う
ため焼結性金属粉末と合成樹脂バインダとを混練した可
塑性物を用い、これを所定の形状に成形し、次いで成形
体中の合成樹脂バインダを熱分解すると共に金属粉末を
焼結することが提案されている。(2) Conventional technology When manufacturing a metal sintered body, in order to facilitate the molding operation, a plastic material made by kneading sinterable metal powder and a synthetic resin binder is used, and this is molded into a predetermined shape. It has been proposed that the synthetic resin binder in the molded body is then thermally decomposed and the metal powder is sintered.
(3)発明が解決しようとする問題点
上記方法において、金属粉末の焼結時それに何等バンク
アップ手段を講じておかないと焼結体が膨張による寸法
変化を惹起し、焼結前後で略4%近い狂いが発生するお
それがある。(3) Problems to be Solved by the Invention In the above method, if no bank-up means is taken during sintering of the metal powder, the sintered body will undergo dimensional changes due to expansion, resulting in approximately There is a possibility that a deviation of nearly % may occur.
本発明は上記に鑑み、簡単な手段により焼結体の膨張を
抑制し得る前記製造方法を提供することを内的とする。In view of the above, it is an object of the present invention to provide the above-mentioned manufacturing method capable of suppressing expansion of a sintered body by simple means.
B0発明の構成
(11問題点を解決するための手段
本発明は、焼結性金属粉末と合成樹脂バインダとを混練
した可塑性物を所定の形状に成形して成形体を得る工程
と、前記成形体を粒状バックアツプ材により包む工程と
、前記成形体中の合成樹脂バインダを熱分解すると共に
前記金属粉末を焼結する工程とを用いることを特徴とす
る。B0 Structure of the Invention (11 Means for Solving Problems) The present invention comprises a step of molding a plastic material obtained by kneading sinterable metal powder and a synthetic resin binder into a predetermined shape to obtain a molded body, and The molded body is characterized by using a step of wrapping the molded body with a granular back-up material, and a step of thermally decomposing the synthetic resin binder in the molded body and sintering the metal powder.
(2)作 用
上記ハックアップ材の押付力により膨張による° 金属
焼結体の寸法変化を抑制して金属焼結体の寸法精度を向
上させるものである。(2) Function The pressing force of the hack-up material suppresses dimensional changes in the metal sintered body due to expansion, thereby improving the dimensional accuracy of the metal sintered body.
(3)実施例
〔実施例I〕
1、可塑性物の製造
Ni自溶性合金粉 80部と、MO粉砕粉 20部とを
■−ブレンダにより十分に混合して混合粉を得る。(3) Example [Example I] 1. Production of plastic material 80 parts of Ni self-fusing alloy powder and 20 parts of MO pulverized powder are sufficiently mixed in a ■-blender to obtain a mixed powder.
四フフ化エチレン樹脂エマルジョンとアクリル樹脂エマ
ルジョンを1:1に混合して合成樹脂バインダを得る。A synthetic resin binder is obtained by mixing a tetrafluoroethylene resin emulsion and an acrylic resin emulsion at a ratio of 1:1.
上記混合粉 100部に対し合成樹脂バインダ3部を添
加して卓上ニーダにより十分に混練し、この混線物を1
00〜150℃に加熱して合成樹脂バインダ中の水分を
蒸発させる。得られた混練物の性状は、合成樹脂バイン
ダにより粘結されて無数の団塊状を呈する。Add 3 parts of synthetic resin binder to 100 parts of the above mixed powder and knead thoroughly using a table kneader.
The water in the synthetic resin binder is evaporated by heating to 00 to 150°C. The obtained kneaded product has a shape of numerous nodules due to being caked by the synthetic resin binder.
上記混練物を80〜lOO℃に加熱してロール機に複数
回通しシート状可塑性物を得る。この場合ロール機のロ
ールを混練物と同程度に加熱するとシート成形作業が容
易に行われる。得られたシート状可塑性物は常温におい
て適度な可撓性と引裂き強度を有する。The above-mentioned kneaded material is heated to 80 to 100° C. and passed through a roll machine several times to obtain a sheet-like plastic material. In this case, if the rolls of the roll machine are heated to the same degree as the kneaded material, the sheet forming operation can be easily performed. The obtained sheet-like plastic material has appropriate flexibility and tear strength at room temperature.
ii 、焼結体の製造
上記シート状可塑性物を用いて、加圧力1kg/m”で
直径20鶴、長さ20龍の円柱状成形体F1〜F、を成
形し、これらに焼結処理を施す。ii. Production of sintered bodies Using the above-mentioned sheet-like plastic material, cylindrical molded bodies F1 to F with a diameter of 20 cranes and a length of 20 dragons are formed using a pressing force of 1 kg/m'', and these are subjected to a sintering treatment. give
焼結処理に当・たり、成形体F、の場合は、第1図(a
、)に示すようにそれを容器1に入れ、その成形体F1
を粒状バックアンプ材としての、直径0.5〜1鶴、線
膨張11 x 10−”/’cの鋼球21により包み、
その容器1を真空焼結炉3に設置する。During the sintering process, in the case of compact F, Figure 1 (a
, ), put it in a container 1, and the molded body F1
is wrapped in a steel ball 21 as a granular back amplifier material with a diameter of 0.5 to 1 Tsuru and a linear expansion of 11 x 10-''/'c,
The container 1 is placed in a vacuum sintering furnace 3.
成形体F2の場合は、第1図(a2)に示すようにそれ
を容器1に入れ、その成形体F2を粒状バックアツプ材
としての、線膨張4 X 10−’/’Cの5号ケイ砂
2□により包み、その容器1を真空焼結炉3に設置する
。In the case of the molded body F2, it is placed in a container 1 as shown in FIG. 1 (a2), and the molded body F2 is placed in a No. Wrapped with sand 2□, the container 1 is placed in a vacuum sintering furnace 3.
成形体F3の場合は、第1図(a3)に示すようにバン
クアップ材無しで真空焼結炉3に設置する。In the case of the compact F3, it is installed in the vacuum sintering furnace 3 without a bank-up material, as shown in FIG. 1 (a3).
そして第2図に示す加熱−冷却条件で有機物質の分解と
金属粉末の焼結を行う。キャリヤガスには窒素ガスまた
は還元性の強い水素ガスが用いられる。Then, the organic substance is decomposed and the metal powder is sintered under the heating-cooling conditions shown in FIG. Nitrogen gas or highly reducing hydrogen gas is used as the carrier gas.
(A)第1加熱ゾーン(第3図A)
この加熱ゾーンAは常温から650℃までであり、昇温
速度は10〜b
熱ゾーンAでは先ず水分が蒸発し、次いで合成樹脂バイ
ンダ中の四フッ化エチレン樹脂およびアクリル樹脂が分
解してガス化する。これら合成樹脂は300〜400℃
でガス化するが、熱伝導を考慮して600〜650℃に
90分間均熱保持して殆どの有機物質を除去し、Ni自
溶性合金−M’。(A) First heating zone (Fig. 3A) This heating zone A is from room temperature to 650°C, and the temperature increase rate is 10~b. In the heating zone A, water first evaporates, and then the Fluorinated ethylene resin and acrylic resin decompose and gasify. These synthetic resins have a temperature of 300 to 400℃
However, in consideration of heat conduction, most of the organic substances were removed by soaking at 600-650°C for 90 minutes, and Ni self-soluble alloy-M' was produced.
粉末よりなる圧粉体を残置する。この場合第1図(al
)、(a、)においてはバックアツプ材としての鋼球2
1およびケイ砂2□は粒状であるがら、生成ガスは鋼球
2□相互間およびケイ砂22相互間の無数の連続気孔を
通じてバックアツプ材より散逸する。A green compact made of powder is left behind. In this case, Figure 1 (al
), (a,), the steel ball 2 is used as a back-up material.
Although 1 and the silica sand 2□ are granular, the generated gas is dissipated from the back-up material through countless continuous pores between the steel balls 2□ and between the silica sand 22.
(B)第2加熱ゾーン(第3図B)
この加熱ゾーンBは900〜1000 ”Cの範囲であ
り、圧粉体をNi自溶性合金の固相線(1010〜10
20℃)以下の温度、例えば950℃に30分間均熱保
持して固相焼結処理を施し、これを仮焼結する。第1加
熱ゾーンAがらの昇温速度は10〜b
真空焼結炉3内の圧粉体は、その表面から加熱されて昇
温するので、圧粉体全体が均一温度に達するまでは所定
の加熱時間が必要である。若し焼結温度である1000
〜1200℃にいきなり加熱すると圧粉体に温度差がで
きて、気孔率のばらつきが多くなり均一な焼結体が得ら
れないだけでなく、焼結後クランク等の欠陥を生じ易く
なる。(B) Second heating zone (Fig. 3B) This heating zone B is in the range of 900 to 1000''C, and the green compact is heated to the solidus line of the Ni self-fluxing alloy (1010 to 10
20° C.) or lower, for example, 950° C., for 30 minutes to perform a solid phase sintering treatment, and then pre-sinter this. The temperature increase rate in the first heating zone A is 10-b.The compact in the vacuum sintering furnace 3 is heated from its surface and increases in temperature, so the temperature rises at a predetermined rate until the entire compact reaches a uniform temperature. Heating time is required. If the sintering temperature is 1000
If it is suddenly heated to ~1200°C, a temperature difference will be created in the green compact, which will increase the variation in porosity, making it impossible to obtain a uniform sintered body, and also making it likely that defects such as cranks will occur after sintering.
第2加熱ゾーンBでは未分解の有機物質が完全にガス化
して除去される。In the second heating zone B, undecomposed organic substances are completely gasified and removed.
(C)第3加熱ゾーン(第3図C)
この加熱ゾーンCは、Ni自溶性合金の固相線(101
0〜1020℃)直下から液相線(1075〜1,08
5℃)を越える温度、即ち1000〜1200℃の範囲
であり、仮焼結体を、例えば液相線を越える温度である
1100〜1180℃、好ましくは1120“Cに12
0分間恒温保持してNi自溶性合金の溶融により液相焼
結処理を施し焼結体を得る。この場合Ni自溶性合金の
流動はMOの存在により妨げられ、したがって形状維持
性が良い。(C) Third heating zone (Fig. 3C) This heating zone C is located at the solidus line (101
0~1020℃) to just below the liquidus line (1075~1,08℃)
5°C), i.e., in the range of 1000 to 1200°C, and the pre-sintered body is heated to a temperature exceeding the liquidus, for example, 1100 to 1180°C, preferably 1120°C, for 12
A sintered body is obtained by holding the temperature at a constant temperature for 0 minutes and performing a liquid phase sintering process by melting the Ni self-fluxing alloy. In this case, the flow of the Ni self-fusing alloy is hindered by the presence of MO, and therefore shape retention is good.
第2加熱ゾーンBからの昇温速度は15〜20’c 7
分であり、仮焼結体は第2加熱ゾーンBで既に高温加熱
されているので、第3加熱ゾーンCまでの昇温時間は僅
かである。この第3加熱ゾーンCの保持時間が不充分で
あると焼結が完全に行われず、焼結体に欠陥を生ずる。The temperature increase rate from the second heating zone B is 15 to 20'c 7
minutes, and since the pre-sintered body has already been heated to a high temperature in the second heating zone B, the time required to raise the temperature to the third heating zone C is short. If the holding time in the third heating zone C is insufficient, sintering will not be completed completely, resulting in defects in the sintered body.
・
(D)冷却ゾーン(第3図D)
この冷却ゾーンDは、前記焼結温度から略800℃まで
の1次冷却ゾーンD、と、略800℃から略400℃ま
での2次冷却ゾーンD2と、略400℃から常温までの
3次冷却ゾーンD3とに分けられる。- (D) Cooling zone (Figure 3 D) This cooling zone D includes a primary cooling zone D from the sintering temperature to approximately 800°C, and a secondary cooling zone D2 from approximately 800°C to approximately 400°C. and a tertiary cooling zone D3 from approximately 400° C. to room temperature.
1次冷却ゾーンD、は、焼結体の高温下における安定域
であり、この冷却ゾーンD、ではできるだけ熱的な刺激
を避け、同時に冷却効率を考慮して最高2℃/分程度の
ゆっくりした速度で冷却する。この冷却ゾーンD、で急
冷が行われると焼結体にクランクが多発する。The primary cooling zone D is a stable region of the sintered body at high temperatures.In this cooling zone D, thermal stimulation is avoided as much as possible, and at the same time, cooling is performed slowly at a maximum rate of about 2°C/min in consideration of cooling efficiency. Cool at speed. When rapid cooling is performed in this cooling zone D, cranks occur frequently in the sintered body.
2次冷却ゾーンD2では、最高3℃/分程度のゆっくり
した速度で冷却する。この冷却ゾーンD2で急冷が行わ
れると焼結体にクランクが多発するおそれがある。In the secondary cooling zone D2, cooling is performed at a slow rate of about 3° C./min at maximum. If rapid cooling is performed in this cooling zone D2, there is a risk that the sintered body will frequently crack.
3次冷却ゾーンD3では、水、油等の液冷以外のガス冷
却(空冷を含む)により焼結体の温度を常温まで冷却す
る。In the tertiary cooling zone D3, the temperature of the sintered body is cooled to room temperature by gas cooling (including air cooling) other than liquid cooling such as water or oil.
上記工程を経て得られた3個の焼結体における焼結処理
前後の長さについて伸び率を測定したところ下表の結果
が得られた。表中、焼結体f、〜f3は成形体F1〜F
3にそれぞれ対応する。When the elongation rate of the three sintered bodies obtained through the above steps was measured before and after the sintering treatment, the results shown in the table below were obtained. In the table, sintered bodies f, ~f3 are molded bodies F1~F
3 respectively.
上記表から明らかなように、可塑性物よりなる成形体F
、〜F3を焼結する場合、バンクアンプ材21.2□を
用いて得られる焼結体f、、f2は、焼結時ハックアッ
プ材21.2□の押付力を受けて膨張が抑制されるので
、バンクアンプ材を用いないで得られる焼結体f3に比
べて伸び率が大幅に減少している。As is clear from the table above, the molded body F made of plastic material
, ~F3, the sintered bodies f, , f2 obtained using the bank amplifier material 21.2□ are suppressed from expanding due to the pressing force of the hack-up material 21.2□ during sintering. Therefore, the elongation rate is significantly reduced compared to the sintered body f3 obtained without using the bank amplifier material.
金型のワーク成形部の形成
第3図(a)に示すように、鋳鋼(JIS SC46材
)よりタンク用金型素材4を鋳造する。この金型素材4
は鋳放しのまま使用されるもので、その黒皮を持つベー
ス面4aには清掃後アクリル樹脂接着剤を塗布する。Formation of the workpiece molding part of the mold As shown in FIG. 3(a), a tank mold material 4 is cast from cast steel (JIS SC46 material). This mold material 4
is used as-cast, and an acrylic resin adhesive is applied to the base surface 4a having a black crust after cleaning.
第3図(b)に示すように、ベース面4aに前記実施例
■と同様のシート状可塑性物を貼着し、雌形模型Mを用
いて0.5 kg/鶴2の圧力を以て押圧し、ワーク形
成部と同一形状の成形体F4を成形する。As shown in FIG. 3(b), a sheet-like plastic material similar to that in Example 2 was pasted on the base surface 4a, and pressed using a female model M with a pressure of 0.5 kg/Tsuru 2. , a molded body F4 having the same shape as the workpiece forming portion is molded.
第3図(c)に示すように、金型素材4を容器1に入れ
、成形体F4をバックアツプ材′としての前記鋼球2I
により包み、その容器1を真空焼結炉3に設置して前記
加熱−冷却条件で成形体F4中の有機物質の分解とN
i自溶性合金−Mo粉末の焼結を行う。As shown in FIG. 3(c), the mold material 4 is placed in the container 1, and the molded body F4 is used as a back-up material' for the steel balls 2I.
The container 1 is placed in the vacuum sintering furnace 3, and the organic substance in the compact F4 is decomposed and the N
i. Sinter the self-fusing alloy-Mo powder.
第3図(d)に示すように、上記工程を経て金型素材4
のベース面4aに、Ni自溶性合金−MO焼結体f4よ
りなるワーク成形部5を持った金型6が得られる。As shown in FIG. 3(d), after the above steps, the mold material 4
A mold 6 having a workpiece forming portion 5 made of a Ni self-fusing alloy-MO sintered body f4 on the base surface 4a is obtained.
上記金型6のワーク成形部5における各部位X〜Zの焼
結前後の厚み方向の伸びを3次元測定機を用いて測定し
たところ、部位Xでは0.2 sva、部位yでは0.
5 mm、部位2では0.1 ml T:あり、ハック
アップ材2Iにより焼結体f、の寸法変化が大幅に抑制
されていることが明らかである。When the elongation in the thickness direction before and after sintering of each part X to Z in the workpiece molding part 5 of the mold 6 was measured using a three-dimensional measuring machine, the elongation in the thickness direction was 0.2 sva in the part X and 0.2 sva in the part y.
5 mm, and 0.1 ml T: in part 2, and it is clear that the dimensional change of the sintered body f is significantly suppressed by the hack-up material 2I.
なお、ハックアップ材としては、mI記鋼球、ケイ砂の
外、球状アルミナ、球状セラミック等を用いることがで
き、必要に応じて鋼球等を水ガラス等の無機バインダに
より部分的に接着して、ハックアップ材を成形体の形状
に合致するように成形してもよい。また第3図(b)工
程におりる可塑性物の成形は、模型Mを用いる場合に限
らず、可塑性物を半硬化させてそれに研削加工を施すよ
うにしてもよい。In addition, as the hack-up material, mI steel balls, silica sand, spherical alumina, spherical ceramics, etc. can be used, and if necessary, the steel balls etc. can be partially bonded with an inorganic binder such as water glass. Then, the hack-up material may be molded to match the shape of the molded article. Further, the molding of the plastic material in the step of FIG. 3(b) is not limited to the case where the model M is used, but the plastic material may be semi-hardened and then subjected to grinding.
C0発明の効果
本発明によれば、可塑性物よりなる成形体を粒状ハック
アップ材による包むという極めて簡単な手段により膨張
による金属焼結体の寸法変化を抑制して、寸法精度の良
い金属焼結体を得ることができる。C0 Effects of the Invention According to the present invention, dimensional changes in the metal sintered body due to expansion are suppressed by an extremely simple method of wrapping a molded body made of a plastic material with a granular hack-up material, and metal sintering with good dimensional accuracy can be achieved. You can get a body.
図面は本発明の実施例を示すもので、第1図(at)〜
(a3)は第1実施例における3個の成形体の焼結処理
を示す説明図、第2図は焼結処理における温度と時間の
関係を示すグラフ、第3図(a)〜(d)は第2実施例
における焼結体の製造工程説明図である。
F、、F、、F4・・・成形体、f4・・・焼結体、2
1,2□・・・バックアツプ材としての鋼球、ケイ砂The drawings show embodiments of the present invention, and are shown in FIG.
(a3) is an explanatory diagram showing the sintering process of three compacts in the first example, FIG. 2 is a graph showing the relationship between temperature and time in the sintering process, and FIGS. 3(a) to (d) FIG. 2 is an explanatory diagram of a manufacturing process of a sintered body in a second example. F,, F,, F4... Molded body, f4... Sintered body, 2
1, 2□・・・Steel balls and silica sand as back-up materials
Claims (1)
物を所定の形状に成形して成形体を得る工程と、前記成
形体を粒状バンクアンプ材により包む工程と、前記成形
体中の合成樹脂バインダを熱分解すると共に前記金属粉
末を焼結する工程と、よりなる金属焼結体の製造方法。A step of molding a plastic material obtained by kneading sinterable metal powder and a synthetic resin binder into a predetermined shape to obtain a molded object, a step of wrapping the molded object with a granular bank amplifier material, and a step of forming a synthetic resin in the molded object. A method for producing a metal sintered body, comprising the steps of thermally decomposing a binder and sintering the metal powder.
Priority Applications (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59077117A JPS60221501A (en) | 1984-04-17 | 1984-04-17 | Production of sintered metallic body |
| IN284/MAS/85A IN164461B (en) | 1984-04-17 | 1985-04-15 | |
| US06/723,030 US4608317A (en) | 1984-04-17 | 1985-04-15 | Material sheet for metal sintered body and method for manufacturing the same and method for manufacturing metal sintered body |
| BE2/60665A BE902203A (en) | 1984-04-17 | 1985-04-16 | MATERIAL LAYER FOR SINTERED METAL BODY AND METHOD FOR MANUFACTURING IT AND METHOD FOR MANUFACTURING A SINTERED METAL BODY |
| BR8501806A BR8501806A (en) | 1984-04-17 | 1985-04-16 | PROCESS FOR THE MANUFACTURE OF A SINTERIZED METAL BODY AND MATERIAL SHEET FOR A SINTERIZED METAL BODY AND PROCESS FOR THE MANUFACTURE OF A MATERIAL SHEET FOR A SINTERIZED METAL BODY |
| KR1019850002591A KR900004597B1 (en) | 1984-04-17 | 1985-04-17 | Material sheet for metal sintered body and method for manufacturing the same and method for manufacturing metal sintered body |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP59077117A JPS60221501A (en) | 1984-04-17 | 1984-04-17 | Production of sintered metallic body |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPS60221501A true JPS60221501A (en) | 1985-11-06 |
Family
ID=13624842
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP59077117A Pending JPS60221501A (en) | 1984-04-17 | 1984-04-17 | Production of sintered metallic body |
Country Status (3)
| Country | Link |
|---|---|
| JP (1) | JPS60221501A (en) |
| KR (1) | KR900004597B1 (en) |
| IN (1) | IN164461B (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4019522B2 (en) * | 1998-10-13 | 2007-12-12 | セイコーエプソン株式会社 | Method for manufacturing sintered body |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53113208A (en) * | 1977-03-15 | 1978-10-03 | Hitachi Funmatsu Yakin Kk | Production of powder metallurgic article |
| JPS5681603A (en) * | 1979-12-10 | 1981-07-03 | Nissan Motor Co Ltd | Sintering method for green material of aluminum powder |
| JPS58113302A (en) * | 1981-12-28 | 1983-07-06 | Nissan Motor Co Ltd | Sintering method for powder molding |
-
1984
- 1984-04-17 JP JP59077117A patent/JPS60221501A/en active Pending
-
1985
- 1985-04-15 IN IN284/MAS/85A patent/IN164461B/en unknown
- 1985-04-17 KR KR1019850002591A patent/KR900004597B1/en not_active Expired
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS53113208A (en) * | 1977-03-15 | 1978-10-03 | Hitachi Funmatsu Yakin Kk | Production of powder metallurgic article |
| JPS5681603A (en) * | 1979-12-10 | 1981-07-03 | Nissan Motor Co Ltd | Sintering method for green material of aluminum powder |
| JPS58113302A (en) * | 1981-12-28 | 1983-07-06 | Nissan Motor Co Ltd | Sintering method for powder molding |
Also Published As
| Publication number | Publication date |
|---|---|
| IN164461B (en) | 1989-03-18 |
| KR850007742A (en) | 1985-12-09 |
| KR900004597B1 (en) | 1990-06-30 |
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