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JPS5852526B2 - Manufacturing method of bronze sintered bearing material - Google Patents
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JPS5852526B2 - Manufacturing method of bronze sintered bearing material - Google Patents

Manufacturing method of bronze sintered bearing material

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Publication number
JPS5852526B2
JPS5852526B2 JP6949279A JP6949279A JPS5852526B2 JP S5852526 B2 JPS5852526 B2 JP S5852526B2 JP 6949279 A JP6949279 A JP 6949279A JP 6949279 A JP6949279 A JP 6949279A JP S5852526 B2 JPS5852526 B2 JP S5852526B2
Authority
JP
Japan
Prior art keywords
temperature
sintering
dewaxing
powder
atmosphere
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
Application number
JP6949279A
Other languages
Japanese (ja)
Other versions
JPS55161005A (en
Inventor
英雄 四方
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.)
Resonac Corp
Original Assignee
Hitachi Powdered Metals 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 Hitachi Powdered Metals Co Ltd filed Critical Hitachi Powdered Metals Co Ltd
Priority to JP6949279A priority Critical patent/JPS5852526B2/en
Priority to GB7931410A priority patent/GB2050429B/en
Publication of JPS55161005A publication Critical patent/JPS55161005A/en
Publication of JPS5852526B2 publication Critical patent/JPS5852526B2/en
Priority to SG687/84A priority patent/SG68784G/en
Expired legal-status Critical Current

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  • Sliding-Contact Bearings (AREA)
  • Powder Metallurgy (AREA)

Description

【発明の詳細な説明】 本発明は、従来品よりも強度の高い青銅系焼結軸受材を
製造する方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for manufacturing a bronze-based sintered bearing material having higher strength than conventional products.

なお青銅系焼結合金の製造においては、青銅の粉末を原
料とする場合と、銅、錫各々の粉末の混合粉を原料とす
る場合とがあるが、本発明の技術は後者の場合を対象と
して開発されたものである。
In the production of bronze-based sintered alloys, there are cases where bronze powder is used as the raw material, and cases where mixed powder of copper and tin powders are used as the raw material, and the technology of the present invention targets the latter case. It was developed as.

はじめに粉末冶金の一般的な工程を述べると、まず原料
粉末にステアリン酸亜鉛その他の粉末状潤滑剤0.3〜
2重量優を添加して充分に混合し、これを金型により所
要の形状に圧縮成形し、次に焼結炉で焼結した後、サイ
ジングおよび含油処理を施して完成するのが標準的な工
程である。
First, to describe the general process of powder metallurgy, first, zinc stearate or other powdered lubricant is added to the raw material powder.
The standard method is to add 2 parts by weight, mix well, compression mold it into the desired shape using a mold, then sinter it in a sintering furnace, and then complete it by sizing and oil impregnation treatment. It is a process.

ここで、焼結合金の材質特性に最も関係の深い焼結工程
に触れると、まず焼結炉の型式は、通常小規模の焼結に
用いられるバッチ型炉と、量産に適する連続型炉とに二
大別される。
Here, we will touch on the sintering process, which is most closely related to the material properties of sintered alloys. First, there are two types of sintering furnaces: batch-type furnaces, which are usually used for small-scale sintering, and continuous-type furnaces, which are suitable for mass production. There are two main categories.

連続型の炉は横に長い管状の炉で、挿入物(成形体)を
移動させる機構によって、たとえば耐熱合金製の鋼ベル
トを用いるメツシュベルト式炉、成形体を入れた焼結箱
を半連続的に順次炉内に押し入れるプッシャ一式炉、そ
の他ローラ一式炉、リフト・ビーム式炉などと種々の方
式があるが、いずれも基本的に&ち炉の入口側から順に
、成形体の予熱・脱ろう室、焼結室、冷却室の3帯域を
備える構造となっている。
Continuous furnaces are horizontally long tube-shaped furnaces that use a mechanism to move the inserts (formed bodies), such as mesh belt furnaces that use heat-resistant alloy steel belts, or semi-continuous sintering boxes containing the formed bodies. There are various methods such as pusher type furnaces, roller type furnaces, lift beam type furnaces, etc., but all of them basically preheat and deheat the compact in order from the inlet side of the furnace. The structure has three zones: a wax chamber, a sintering chamber, and a cooling chamber.

なお、炉内の雰囲気としては、一般に水素ガスあるいは
アンモニア分解ガスなどの還元性雰囲気が用いられてい
る。
Note that, as the atmosphere in the furnace, a reducing atmosphere such as hydrogen gas or ammonia decomposition gas is generally used.

次に焼結工程は、前段の脱ろう工程と、後段の本焼結工
程との二段階に分けられる。
Next, the sintering process is divided into two stages: an earlier dewaxing process and a later main sintering process.

即ち、成形体が前述の炉内を通過する間に、まず比較的
低温の予熱・脱ろう室で成形体中の潤滑剤を蒸発させて
除去し、次いで所定の高温に保たれた焼結炉で本格的に
焼結された後、常温近くまで徐冷されて焼結工程を終了
する。
That is, while the compact passes through the above-mentioned furnace, the lubricant in the compact is first evaporated and removed in a relatively low-temperature preheating/dewaxing chamber, and then in a sintering furnace maintained at a predetermined high temperature. After being sintered in earnest, it is gradually cooled to near room temperature to complete the sintering process.

ここで、脱ろつ温度は約400℃、この温度に至る昇温
速度は毎分lO〜30℃、本焼結温度は約780℃なる
条件が、青銅系における従来の標準的焼結条件である。
Here, the conditions are that the dewaxing temperature is approximately 400°C, the temperature increase rate to reach this temperature is 10 to 30°C per minute, and the main sintering temperature is approximately 780°C. be.

第1図のグラフ&転成形体が上述の焼結工程で受ける熱
履歴を表わしたもので、図中←A→の範囲が脱ろう工程
に、←B→の範囲が本焼結および冷却工程に相当する。
The graph in Figure 1 shows the thermal history that the rolled compact undergoes in the above-mentioned sintering process. Equivalent to.

さて、このようにして還元性雰囲気中で脱ろうおよび焼
結して得られる青銅系焼結合金は、その強度が圧環強度
で18V4/uIt2を僅かに上回る程度である。
Now, the bronze-based sintered alloy obtained by dewaxing and sintering in a reducing atmosphere in this manner has a strength slightly exceeding 18V4/uIt2 in terms of radial crushing strength.

そこで、含油軸受も機械要素の一種である以上、設計の
自由度を増すためにもその強度をできるだけ高めること
が望まれている。
Therefore, since oil-impregnated bearings are also a type of mechanical element, it is desired to increase their strength as much as possible in order to increase the degree of freedom in design.

しかし、軸受材の高強度化はそう容易なことではない。However, increasing the strength of bearing materials is not so easy.

何故ならば、含油軸受の場合はそれ自身の耐摩耗性と共
に相手部材の軸をも摩耗させないこと、さらに、できる
だけ多孔質で、多量の潤滑油な含浸保持できることが必
須の条件であって、従って、例えば歯車などの機械構成
部品の場合のように、強化成分の添力11によって高合
金化するとか、あるいは高圧で圧縮成形して部材を緻密
化するなどの、粉末冶金における一般的な強化方法が採
用できないからである。
This is because in the case of an oil-impregnated bearing, it is essential that it not only has its own wear resistance, but also that it does not wear out the shaft of the mating member, and that it is as porous as possible and capable of retaining a large amount of lubricating oil. , common strengthening methods in powder metallurgy, such as high alloying with the addition of reinforcing components 11, as in the case of mechanical components such as gears, or densification of parts by compression molding at high pressure. This is because it cannot be adopted.

そこで発明者は、専ら成形体の焼結工程の研究に努めた
結果、その前段である予熱・脱ろう工程の改良によって
、本来の軸受特性を保ちながらその強度を向上させるこ
とに成功した。
Therefore, the inventor devoted his efforts to researching the sintering process of the compact, and by improving the preheating and dewaxing process that precedes it, he succeeded in improving the strength of the bearing while maintaining its original characteristics.

※※ この改良点即ち本発明の性徴は、脱
ろう工程における脱ろう温度を従来法よりも高めの41
5〜710℃とすることと、それぞれ還元性雰囲気中で
行なわれる脱ろうと、それに続く本焼結工程との間に、
酸化性雰囲気中での酸化反応工程を介在させることを骨
子とするものである。
※※ This improvement, that is, the characteristic of the present invention, is that the dewaxing temperature in the dewaxing process is 41% higher than that of the conventional method.
5 to 710°C, dewaxing carried out in a reducing atmosphere, and the subsequent main sintering process.
The main point of this method is to include an oxidation reaction step in an oxidizing atmosphere.

なお、ここにいう酸化性雰囲気としては特別な酸化性ガ
スを用いてもよいが、通常は大気を用いることによって
、簡便にその目的を達することが可能である。
Note that although a special oxidizing gas may be used as the oxidizing atmosphere here, the purpose can usually be easily achieved by using the atmosphere.

以下本発明をその一実施例について説明する。The present invention will be described below with reference to one embodiment thereof.

まず銅粉と錫粉とを銅91%、賂9優の割合に配合し、
その全量に対して0.3%のステアリン酸亜鉛を潤滑剤
として添加して充分に混合し、この混合粉を金型に入れ
て圧縮し、形が外径18m、内径101EJI、長さ1
4130円筒状で、圧粉密度が6.35t/crILの
試料多数を成形する。
First, copper powder and tin powder are mixed in a ratio of 91% copper and 9% copper,
Add 0.3% zinc stearate as a lubricant to the total amount, mix thoroughly, put this mixed powder into a mold and compress it, and the shape is 18 m in outer diameter, 101 EJI in inner diameter, and 1 in length.
A large number of samples with a cylindrical shape of 4130 and a green powder density of 6.35 t/crIL are molded.

次に試料の焼結については、脱ろう室と本焼結室とが分
離され、両者をメツシュベルトで連結した型式の連続焼
結炉を用い、上記の試料なI〜■の群に分けて、それぞ
れを第1表に記した脱ろう条件に基づいて焼結する。
Next, regarding the sintering of the samples, a continuous sintering furnace of the type in which the dewaxing chamber and the main sintering chamber are separated and both are connected by a mesh belt is used, and the samples are divided into the above groups I to ■. Each was sintered based on the dewaxing conditions listed in Table 1.

即ち、表中試料■の群は本発明に係るもので、まず試料
を還元性雰囲気の脱ろう室に送り込み、毎分30℃の昇
温速度で700℃まで上昇させて数分間保持し、潤滑剤
を蒸発させる。
That is, the sample group ① in the table is related to the present invention. First, the sample is sent to a dewaxing chamber with a reducing atmosphere, and the temperature is raised to 700 °C at a rate of 30 °C per minute, held for several minutes, and then lubricated. Evaporate the agent.

昇温速度は炉室内の温度分布および送り速度の調節によ
って任意に設定することができる。
The temperature increase rate can be arbitrarily set by adjusting the temperature distribution in the furnace chamber and the feed rate.

次に、脱ろう後の試料を脱ろう室から大気(酸化性雰囲
気)中に移し、その表面を酸化させる。
Next, the dewaxed sample is transferred from the dewaxing chamber to the atmosphere (oxidizing atmosphere) to oxidize its surface.

なおこの間に試料の温度が低下するが、これは焼結結果
には殆ど影響しない。
Although the temperature of the sample decreases during this time, this has little effect on the sintering results.

続いて、試料の本焼結が還元性雰囲気中780℃の温度
を約15分間保持して行なわれ、以後通常の冷却工程を
経て焼結を完了する。
Subsequently, main sintering of the sample is carried out in a reducing atmosphere by maintaining the temperature at 780° C. for about 15 minutes, and then a normal cooling process is performed to complete the sintering.

なお第2図のグラフは、試料■が上述の工程で受ける熱
履歴を表わしたもので、図中←AI→の範囲が還元性雰
囲気中での予熱・脱ろう工程に、それに続く←AII→
の範囲が酸化性雰囲気中での酸化反応工程に、また、←
B→の範囲が還元性雰囲気中での本焼結および冷却工程
に相当する。
The graph in Figure 2 shows the thermal history that sample ■ undergoes in the above process.
For the oxidation reaction process in an oxidizing atmosphere, the range of ←
The range B→ corresponds to the main sintering and cooling steps in a reducing atmosphere.

かくして焼結された試料■について、その圧環強度をJ
IS Z2507(ISO2739)に従って測定し
たところ、30Ky/Jの高い値を示した。
For the sample ■ thus sintered, its radial crushing strength is J
Measurement according to IS Z2507 (ISO2739) showed a high value of 30 Ky/J.

これに対して、表中試料■の群は、脱ろう工程を従来の
方法、即ち脱ろう室と本焼結室を気密に連結して炉内の
雰囲気を還元性雰囲気とし、先ず毎分30℃の昇温速度
で400℃まで上昇させて脱ろうし、引き続き試料■の
場合と同一の条件で焼結したものであり、その圧環強度
は19〜〆−2であった。
On the other hand, for the group of samples (2) in the table, the dewaxing process was carried out using the conventional method, that is, the dewaxing chamber and the main sintering chamber were airtightly connected to create a reducing atmosphere in the furnace. The sample was dewaxed by raising the temperature to 400°C at a heating rate of 10°C, and then sintered under the same conditions as Sample 1, and its radial crushing strength was 19 to -2.

次に試料■の群は、試料■に示す従来の脱ろう条件の一
部を変えた、即ち脱ろつ温度を400℃から700℃に
高めたもので、温度が高いだけにその圧環強度も従来よ
り僅かに上昇しているが、しかし、とくに有意と認めら
れるほどではない。
Next, the sample group (2) is one in which some of the conventional dewaxing conditions shown in sample (2) are changed, that is, the dewaxing temperature is increased from 400°C to 700°C. Although it is slightly higher than before, it is not significant enough.

次に試料■の群は、本発明と同じ〈従来方法の改良技術
として、本発明者が別途提案した脱ろう方法に基づく例
である。
Next, sample group (2) is an example based on the same method as the present invention (a dewaxing method separately proposed by the present inventor as an improved technique of the conventional method).

この方法の従来方法との違いは、脱ろう工程が終始酸化
性雰囲気中で行なわれることと、脱ろう時の昇温速度を
毎分50℃以上と従来の毎分10〜30℃に比べ高速に
したことであり、この改良により、26〜メム2という
従来より著しく高い圧環強度が得られる。
The difference between this method and the conventional method is that the dewaxing process is carried out in an oxidizing atmosphere throughout, and the temperature increase rate during dewaxing is faster than 50°C per minute, compared to the conventional 10-30°C. With this improvement, a radial crushing strength of 26 to 2 mem, which is significantly higher than the conventional one, can be obtained.

但し、本発明による焼結材がこれより更に高強度を示す
ことは、前述の通りである。
However, as described above, the sintered material according to the present invention exhibits even higher strength than this.

なお、以上4種の試料にサイジングおよび含油を施して
軸受に仕上げ、軸受性能試験機にかけて比較試験をした
ところ、いずれもほぼ同等の特性を示し、格別の有意差
は認められなかった。
Furthermore, when the four types of samples mentioned above were sized and oil-impregnated into bearings and then subjected to a comparative test using a bearing performance tester, all of them showed almost the same characteristics, and no particularly significant difference was observed.

そこで更に実験を重ねて、本発明において圧環強度が顕
著に向上する限界条件を求めたところ、昇温速度は従来
同様に毎分10〜30℃でよく、要は脱ろ5温度な液相
の生じない温度範囲、即ち銅−錫系平衡状態図における
L−ε→η包晶温度(415℃)より高く液相発生温度
(γ+Lの領域に接するγの固相線とε相の組成の延長
線との交点で、710℃に相当する)より低い範囲内と
して、この温度から酸化反応工程に移れば試料■に代表
される従来法よりも優れた結果が得られることが判明し
た。
After repeated experiments, we determined the critical conditions under which the radial crushing strength of the present invention would be significantly improved.We found that the temperature increase rate could be 10 to 30 degrees Celsius per minute, as in the case of the conventional method, and that the temperature rise rate of the liquid phase at the 5-temperature of the removal temperature was sufficient. The temperature range in which this does not occur is higher than the L-ε→η peritectic temperature (415°C) in the copper-tin system equilibrium phase diagram, and the liquid phase generation temperature (the extension of the solidus line of γ and the composition of the ε phase in contact with the γ+L region) It was found that if the oxidation reaction step was carried out from this temperature within a lower range (corresponding to 710° C. at the intersection with the line), results superior to the conventional method typified by sample ① could be obtained.

以上の結果に明らかなように、本発明によれば従来品よ
り以上の高強度の軸受材が、また、強度は従来程度でよ
い場合にはより高含油率の軸受材が得られ、従って、本
発明は青銅系焼結含油軸受の適用範囲の拡大に大きく寄
与するものである。
As is clear from the above results, according to the present invention, a bearing material with higher strength than the conventional product can be obtained, and if the strength is the same as the conventional product, a bearing material with a higher oil content can be obtained. The present invention greatly contributes to expanding the range of application of bronze-based sintered oil-impregnated bearings.

さて、以上で本発明の構成およびその効果を詳述したが
、最後に、本発明による作用効果の原理について考察す
る。
Now, the structure of the present invention and its effects have been described in detail above, and finally, the principle of the operation and effect of the present invention will be considered.

先ず、粉末粒子間に潤滑剤が介在しない(即ち金型潤滑
法で成形された)成形体における、純然たる焼結現象に
のみ着目すれば、粉末の表面がある程度酸化されている
方が以後の焼結がより良く進行する。
First, if we focus only on the pure sintering phenomenon in a molded body in which no lubricant is present between the powder particles (that is, molded by the mold lubrication method), it is better to have the surface of the powder oxidized to some extent. Sintering progresses better.

これは、還元性雰囲気中での焼結の過程で酸化膜が還元
され、粒表面が活性にな−るためである。
This is because the oxide film is reduced during the sintering process in a reducing atmosphere and the grain surface becomes active.

従って、この意味からは、酸化性雰囲気中での予熱・脱
ろうに有利な点が認められるが、他方、この方式には次
のような不利な点がある。
Therefore, from this point of view, preheating and dewaxing in an oxidizing atmosphere is advantageous, but on the other hand, this method has the following disadvantages.

即ち、酸化性雰囲気中での加熱により生成される酸化物
によって成形体の表面および内部の空孔が被覆される結
果、成形体内部からの潤滑剤の蒸発飛散が阻害され、さ
らに、潤滑剤組成中のカーボン物質がすす状になって残
留し、その結果、粉末相互の拡散焼結が十分に行なわれ
なくなる。
That is, as a result of coating the surface and internal pores of the molded body with oxides generated by heating in an oxidizing atmosphere, the evaporation and scattering of the lubricant from inside the molded body is inhibited, and furthermore, the lubricant composition The carbon material therein remains in the form of soot, and as a result, the powders are not sufficiently diffused and sintered.

そしてこのマイナスの方が、活性化焼結によるプラスよ
り大きい。
And this minus is greater than the plus due to activated sintering.

これが従来、成形体の予熱・脱ろうを還元性の雰囲気中
で行なっている大きな理由である。
This is the main reason why molded bodies are conventionally preheated and dewaxed in a reducing atmosphere.

これに対して、本発明の説明に入る前に、先ず試料■に
示した改良方法の得失について触れる。
On the other hand, before going into the explanation of the present invention, we will first discuss the advantages and disadvantages of the improved method shown in sample (2).

この方法は、予熱・脱ろうの全工程を酸化性雰囲気中で
、しかも毎分50℃以上の高速で昇温させながら行なう
ことにより、先ず潤滑剤の脱ろうが先行し、その後に成
形体の酸化反応が進行するように両反応を制御し、もっ
て軸受特性を低下させずに高強度化を達成できたもので
あるが、しかしその反面、酸化性雰囲気下に液相を経る
ため組織および寸法変化が不安定になり易いこと、高速
で昇温させる必要上、とくに一連のメツシュベルト式炉
の場合など、炉体を改造して延長しなげればならないこ
となどの問題がある。
In this method, the entire process of preheating and dewaxing is carried out in an oxidizing atmosphere while raising the temperature at a high rate of 50°C or more per minute, so that the lubricant is first dewaxed, and then the molded body is dewaxed. By controlling both reactions so that the oxidation reaction progresses, high strength can be achieved without degrading the bearing properties.However, on the other hand, because the bearing undergoes a liquid phase in an oxidizing atmosphere, its structure and dimensions deteriorate. Problems include the tendency for changes to become unstable, the need to raise the temperature at high speeds, and the need to modify and extend the furnace body, especially in the case of series meshbelt furnaces.

しかるに、本発明においては予熱・脱ろうの際の雰囲気
が還元性なので、潤滑剤の脱ろうが円滑に行なわれる。
However, in the present invention, since the atmosphere during preheating and dewaxing is reducing, the lubricant can be smoothly dewaxed.

また、この際の昇温速度も従来の標準速度でよく、従っ
て炉長その他に対する配慮も不必要である。
In addition, the temperature increase rate at this time may be the conventional standard rate, and therefore there is no need to consider the furnace length or the like.

脱ろう完了後、成形体を酸化性雰囲気中に移してその表
面を酸化させるが、これが固相域である415〜710
’Cの温度範囲から行なわれるために、組織および寸
法変化への影響が防止されるものである。
After the dewaxing is completed, the molded body is transferred to an oxidizing atmosphere to oxidize its surface, which is the solid phase region of 415 to 710.
Since the process is carried out in the temperature range of 1000 C, effects on the structure and dimensional changes are prevented.

かくして完全な脱ろうと活性化焼結の利用とが共に達成
され、その結果として従来法に比べて高強度の軸受材が
得られるものと考えられる。
In this way, it is believed that both complete dewaxing and the use of activated sintering are achieved, resulting in a bearing material with higher strength compared to conventional methods.

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

第1図は従来の焼結工程における熱履歴を示す温度一時
間特性図、第2図は本発明の焼結工程における熱履歴を
示す温度一時間特性図である。 AI・・・予熱・脱ろう工程、AII・・・酸化工程、
・・・本焼結工程。
FIG. 1 is a temperature one-hour characteristic diagram showing the thermal history in a conventional sintering process, and FIG. 2 is a temperature one-hour characteristic diagram showing the thermal history in the sintering process of the present invention. AI... preheating/dewaxing process, AII... oxidation process,
...Main sintering process.

Claims (1)

【特許請求の範囲】 1 銅粉および錫粉等を原料として粉末冶金法により軸
受材を製造する方法において、銅粉、錫粉および潤滑剤
を所定の割合で混合して所定の形状に成形した後、還元
性雰囲気中で銅−錫状態図におけるL十ε→η包晶温度
(415℃)より高く液相発生温度(710℃)より低
い温度範囲内に一定時間保持することにより前記潤滑剤
を蒸発させて除去すると同時に仮焼結を行ない、次にこ
の成形体を酸化性雰囲気中に数分間保持して固相状態で
酸化反応を生じさせ、次いで還元性雰囲気中で液相焼結
を行なうことを特徴とする青銅系焼結軸受材の製造法。 2 上記酸化性雰囲気として大気を用いることを特徴と
する特許請求の範囲第1項記載の青銅系焼結軸受材の製
造法。
[Claims] 1. A method for manufacturing bearing materials by powder metallurgy using copper powder, tin powder, etc. as raw materials, in which copper powder, tin powder, and lubricant are mixed in a predetermined ratio and formed into a predetermined shape. After that, the lubricant is maintained in a reducing atmosphere for a certain period of time within a temperature range higher than the L1ε→η peritectic temperature (415°C) and lower than the liquid phase generation temperature (710°C) in the copper-tin phase diagram. At the same time as evaporation and removal, temporary sintering is performed, and then this compact is held in an oxidizing atmosphere for several minutes to cause an oxidation reaction in the solid state, and then liquid phase sintering is performed in a reducing atmosphere. A method for producing a bronze-based sintered bearing material. 2. The method for manufacturing a bronze-based sintered bearing material according to claim 1, characterized in that the atmosphere is used as the oxidizing atmosphere.
JP6949279A 1979-06-05 1979-06-05 Manufacturing method of bronze sintered bearing material Expired JPS5852526B2 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
JP6949279A JPS5852526B2 (en) 1979-06-05 1979-06-05 Manufacturing method of bronze sintered bearing material
GB7931410A GB2050429B (en) 1979-06-05 1979-09-11 Method of producing bronze-based sintered bearing material
SG687/84A SG68784G (en) 1979-06-05 1984-09-25 Method of producing bronze-based sintered bearing material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6949279A JPS5852526B2 (en) 1979-06-05 1979-06-05 Manufacturing method of bronze sintered bearing material

Publications (2)

Publication Number Publication Date
JPS55161005A JPS55161005A (en) 1980-12-15
JPS5852526B2 true JPS5852526B2 (en) 1983-11-24

Family

ID=13404252

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6949279A Expired JPS5852526B2 (en) 1979-06-05 1979-06-05 Manufacturing method of bronze sintered bearing material

Country Status (1)

Country Link
JP (1) JPS5852526B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0692604B2 (en) * 1989-11-30 1994-11-16 川崎製鉄株式会社 Method for producing iron-based metal sintered body by metal powder injection molding
CN113399672A (en) * 2021-06-21 2021-09-17 扬州保来得科技实业有限公司 Cu-10Sn bronze powder and preparation method and application thereof

Also Published As

Publication number Publication date
JPS55161005A (en) 1980-12-15

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