JPS5914537B2 - Sintered sliding parts - Google Patents
Sintered sliding partsInfo
- Publication number
- JPS5914537B2 JPS5914537B2 JP11748876A JP11748876A JPS5914537B2 JP S5914537 B2 JPS5914537 B2 JP S5914537B2 JP 11748876 A JP11748876 A JP 11748876A JP 11748876 A JP11748876 A JP 11748876A JP S5914537 B2 JPS5914537 B2 JP S5914537B2
- Authority
- JP
- Japan
- Prior art keywords
- sintered sliding
- sliding parts
- sintered
- powder
- cu2s
- 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
Links
Landscapes
- Powder Metallurgy (AREA)
Description
【発明の詳細な説明】
本発明は粉末冶金法による高温での耐摩性、耐酸化性に
優れた摺動部材に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a sliding member manufactured by powder metallurgy that has excellent wear resistance and oxidation resistance at high temperatures.
焼結合金は複合性に優れ、耐摩性に富む硬質成分の分散
と併せて、低融点金属や、硫黄化合物の如き潤滑性に富
む成分を同時に含有せしめ、耐摩摺動特性を改善するこ
とが可能である。Sintered alloys have excellent composite properties, and in addition to dispersing hard components with high wear resistance, it is possible to simultaneously contain low melting point metals and components with high lubricity such as sulfur compounds, thereby improving the wear and sliding properties. It is.
本発明はこの考えに基き、安価で耐摩性に優れた摺動材
料を提供せんとするもので、本発明材は以下の様な方法
で作られる鉄粉にCrあるいはFe−Cr粉をCr%で
8〜30%、MoあるいはFe−Mo粉をMo%で0.
2% 〜5%、Cu2S又はW2Sを5〜15φ、炭素
粉0.1〜2.0係と少量の成形用型潤滑剤を加え、混
合、プレス成形後1000〜1150℃の還元性雰囲気
中で焼結して得られる。Based on this idea, the present invention aims to provide a sliding material that is inexpensive and has excellent wear resistance. 8 to 30%, Mo or Fe-Mo powder at Mo% of 0.
Add 2% to 5% of Cu2S or W2S to 5 to 15φ, carbon powder of 0.1 to 2.0 mm, and a small amount of mold lubricant, mix and press mold in a reducing atmosphere at 1000 to 1150°C. Obtained by sintering.
成分中Crは鉄中に固溶しマトリックスの耐熱性と耐酸
化性をCと共存した場合一部炭化物となって析出し耐摩
性向上に役立て、8%以下ではこれらの効果が充分でな
く、又30%を超えても材質的に脆くなり加工性が低下
するので好ましい組成範囲を8〜30係とした。Cr in the component dissolves in iron and improves the heat resistance and oxidation resistance of the matrix. When it coexists with C, it partially precipitates as carbide and helps improve wear resistance. If it is less than 8%, these effects are not sufficient. Moreover, if it exceeds 30%, the material becomes brittle and workability decreases, so the preferred composition range is set to 8 to 30%.
Moの添加はFe −Cr系に於て耐熱性、耐酸化性の
改善に有効であるが0.2%以下ではその効果が小さく
、5%以上になると加工性が悪くなる。Addition of Mo is effective in improving heat resistance and oxidation resistance in Fe-Cr systems, but if it is less than 0.2%, the effect is small, and if it is more than 5%, workability deteriorates.
Cは本系に添加された場合、マトリックスはマルテンサ
イト組織となり著しく硬化し耐摩性、耐熱性が改善され
、0.1楚以下ではその効果が殆んどないが2%以上と
なっても炭化物が網状に析出し脆化するので量的に0.
1〜2係の範囲が好ましい。When C is added to this system, the matrix becomes a martensitic structure, which hardens significantly and improves wear resistance and heat resistance.If C is less than 0.1%, there is almost no effect, but if it is more than 2%, carbide formation occurs. is precipitated in a network and becomes brittle, so the quantity is 0.
A range of 1 to 2 is preferable.
Cu25−WS2は本系に於て潤滑成分として添加され
るものである。Cu25-WS2 is added as a lubricating component in this system.
一般に硫黄ないし硫黄化合物は潤滑性を示すことが知ら
れているが、実際にこれらを含有する焼結体を得ること
は還元雰囲気中で、これらの化合物が簡単に分解してし
まい焼結を害するのでかなり難かしい。It is generally known that sulfur or sulfur compounds exhibit lubricity, but actually obtaining a sintered body containing these compounds is difficult because these compounds easily decompose in a reducing atmosphere, impairing sintering. So it's quite difficult.
数多くの硫黄化合物のうち硫化第一銅(Cu2S)
と硫化タングステンは比較的高温まで安定(硫化第一銅
の融点→1130℃1130℃硫化タングステラ℃まで
安定)で1000〜1150℃の焼結温度であれば、こ
れらの硫黄化合物は、焼結後もほぼ完全な形で焼結体中
に残存する。Among many sulfur compounds, cuprous sulfide (Cu2S)
and tungsten sulfide are stable up to relatively high temperatures (melting point of cuprous sulfide → stable up to 1130℃ 1130℃ tungsten sulfide ℃), and if the sintering temperature is 1000 to 1150℃, these sulfur compounds will remain stable even after sintering. It remains in the sintered body in almost perfect form.
潤滑成分としての機能は5係以下の添加では充分と云え
ず、又15%を超えても強度低下が大きくなる為、5〜
15係の範囲の添加が好ましい。The function as a lubricating component cannot be said to be sufficient if the addition ratio is less than 5%, and even if it exceeds 15%, there will be a significant decrease in strength.
It is preferable to add in a range of 15%.
以下実施例にて詳細に述べることにする。This will be described in detail in Examples below.
〈実施例〉
一325メツシュのクロウム又はフェロクロウム粉末、
同じ<−325メツシユのモリブデン又はフェロモリブ
デン粉末とグラファイト粉末及びCu2S、WS2粉末
、−100メツシユの鉄粉を下記組成割合に配合、混合
後85%の密度に成形し、その後に1230℃で1時間
焼結(雰囲気は水素)を行った。<Example> 1325 mesh chromium or ferrochrome powder,
Molybdenum or ferromolybdenum powder of the same <-325 mesh, graphite powder, Cu2S, WS2 powder, and iron powder of -100 mesh were mixed in the following composition ratio, and after mixing, molded to a density of 85%, and then heated at 1230°C for 1 hour. Sintering (in hydrogen atmosphere) was performed.
得られた焼結材に対し高温での摩耗試験を実施した。A high-temperature wear test was conducted on the obtained sintered material.
比較材としてFe12、リン青銅、焼結合金Fe−0,
3P−5M o−I C−3P bを選び同時に試験を
行った。Fe12, phosphor bronze, sintered alloy Fe-0,
3P-5Mo-I C-3P b were selected and tested at the same time.
以上の結果より明らかの様に自己潤滑成分として硫化第
一銅ないしは硫化タングステンを含有するフェライト及
びマルテンサイト系組成の焼結材料は耐摩性の優れてい
る材料として良く知られている鋳鉄やリン青銅あるいは
鉛成分を含有する焼結合金を上回る高温、酸化雰囲気中
での耐摩性、耐焼き付き性を示した。As is clear from the above results, sintered materials with ferritic and martensitic compositions containing cuprous sulfide or tungsten sulfide as a self-lubricating component are better suited to cast iron and phosphor bronze, which are well known as materials with excellent wear resistance. Moreover, it exhibited wear resistance and seizure resistance at high temperatures and in an oxidizing atmosphere that exceeded that of sintered alloys containing lead components.
これは本発明材が耐熱性と耐酸化性に富むマ) IJラ
ック常温から比較的高温までの巾広い温度域で優れた潤
滑性を発揮する硫黄化合物から構成されていることによ
るものと思われる。This is thought to be due to the fact that the material of the present invention is composed of a sulfur compound that exhibits excellent lubricity over a wide temperature range from room temperature to relatively high temperatures. .
Claims (1)
5〜15%、残り鉄の組成より成る焼結摺動部材 2 重量係でCr:8〜30%、Mo : 0.2〜5
%、Cu2S又はWS2 :5〜15係、残り鉄の組成
より成る焼結摺動部材 3 重量係でCr:8〜30%、Mo : 0.2〜5
係、C:0.1〜2.0%、Cu2S又はWS2 :5
〜15%、残り鉄の組成より成る焼結摺動部材[Claims] 1. Cr: 8 to 30% by weight, Cu2S or WS2:
Sintered sliding member 2 consisting of a composition of 5 to 15% and remaining iron; Cr by weight: 8 to 30%, Mo: 0.2 to 5
%, Cu2S or WS2: 5-15%, remaining iron composition Sintered sliding member 3 Weight: Cr: 8-30%, Mo: 0.2-5
C: 0.1-2.0%, Cu2S or WS2: 5
Sintered sliding member consisting of ~15% residual iron composition
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11748876A JPS5914537B2 (en) | 1976-09-29 | 1976-09-29 | Sintered sliding parts |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11748876A JPS5914537B2 (en) | 1976-09-29 | 1976-09-29 | Sintered sliding parts |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5342109A JPS5342109A (en) | 1978-04-17 |
JPS5914537B2 true JPS5914537B2 (en) | 1984-04-05 |
Family
ID=14712948
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11748876A Expired JPS5914537B2 (en) | 1976-09-29 | 1976-09-29 | Sintered sliding parts |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5914537B2 (en) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0310037B1 (en) * | 1987-09-28 | 1993-07-14 | Kuraray Co., Ltd. | Leather-like sheet material and method of producing same |
JPH0772318B2 (en) * | 1990-08-30 | 1995-08-02 | 帝国カーボン工業株式会社 | Manufacturing method of ferrous wear-resistant sintered alloy for current collecting sliding |
JPH0772319B2 (en) * | 1990-08-30 | 1995-08-02 | 帝国カーボン工業株式会社 | Manufacturing method of ferrous wear-resistant sintered alloy for current collecting sliding |
-
1976
- 1976-09-29 JP JP11748876A patent/JPS5914537B2/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
JPS5342109A (en) | 1978-04-17 |
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