JPH0285338A - Iron-based sintered sliding material - Google Patents
Iron-based sintered sliding materialInfo
- Publication number
- JPH0285338A JPH0285338A JP23558588A JP23558588A JPH0285338A JP H0285338 A JPH0285338 A JP H0285338A JP 23558588 A JP23558588 A JP 23558588A JP 23558588 A JP23558588 A JP 23558588A JP H0285338 A JPH0285338 A JP H0285338A
- Authority
- JP
- Japan
- Prior art keywords
- iron
- steadite
- sliding material
- based sintered
- heat treatment
- 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
Landscapes
- Powder Metallurgy (AREA)
Abstract
(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。(57) [Abstract] This bulletin contains application data before electronic filing, so abstract data is not recorded.
Description
【発明の詳細な説明】
(ti業上の利用分野)
本発明は、エンジンのシリンダライナや軸受は等、高速
油潤滑時の耐Jツ耗鉄系焼結摺動材料に関する。DETAILED DESCRIPTION OF THE INVENTION (Field of Application in Ti Industry) The present invention relates to a wear-resistant iron-based sintered sliding material for engine cylinder liners, bearings, etc. during high-speed oil lubrication.
(従来の技術)
従来、耐摩耗鋳鉄の場合、Fe−C−P系のステゲイト
組織を析出させ耐摩耗性を持たせている。(Prior Art) Conventionally, in the case of wear-resistant cast iron, a Fe-C-P-based stegate structure is precipitated to impart wear resistance.
P成分を0.7%以上添加した焼結部材は、焼結時ステ
ダイトがFe粉粒子界面に液相として出現するため、ネ
ット状で析出した部材となる。(発明C発明が解決しよ
うとする課題)
前記従来の技術に於て、耐摩耗鋳鉄を鋳造する場合、i
5加できるFe−C,−Pの量は品質的安定性を号慮す
ると、0.7%が上限である。また、Pを0.7% 以
上添加した焼結材はステダイトがネット状に析出するた
め、靭性が下がり摺動材として好ましくない欠点があっ
た。一般に摺動材料としては限界pv値が4000 (
kg/cm−m /5ec)以上が、事実上好ましいと
されCいる。In a sintered member to which 0.7% or more of the P component is added, steadite appears as a liquid phase at the Fe powder particle interface during sintering, resulting in a member precipitated in a net shape. (Problem to be solved by Invention C) In the conventional technology, when casting wear-resistant cast iron, i
The upper limit of the amount of Fe-C and -P that can be added is 0.7%, considering quality stability. In addition, sintered materials containing 0.7% or more of P have the disadvantage that steadite precipitates in the form of a net, resulting in a decrease in toughness and making them undesirable as sliding materials. Generally, the limit pv value for sliding materials is 4000 (
kg/cm-m/5ec) or more is actually considered preferable.
(課題を解決するための手段)
本発明は前記従来の技術に於ける課題を解決するために
成されたもので、
重量比でNi:Q、2〜4%、Cr:0.5〜3%、M
o:0.05〜2%のうちから選ばれた1種以上を総量
で0.1〜5%含み、残部が実質的にFeがら成る合金
鋼粉に、黒鉛とリン−合金粉及び必要があ11゜ば純鉄
粉及び他合金粉を混合し、重量比でC018〜1.4%
、p:o、6〜1.0%から成る焼結部材を焼結した後
、850℃〜tooo℃で溶体化熱処理を施し、析出し
たステダイトを球状化処理したことを特徴とする鉄系焼
結摺動材料により構成して目的を達成するようにした。(Means for Solving the Problems) The present invention has been made to solve the problems in the above-mentioned conventional technology, and includes a weight ratio of Ni: Q, 2 to 4%, Cr: 0.5 to 3. %, M
o: Alloy steel powder containing one or more selected from 0.05 to 2% in a total amount of 0.1 to 5%, with the remainder substantially consisting of Fe, graphite and phosphorus alloy powder, and as necessary. A11: Mix pure iron powder and other alloy powder, and make CO18~1.4% by weight.
, p:o, 6 to 1.0% is sintered, and then subjected to solution heat treatment at 850°C to tooo°C, and the precipitated steadite is spheroidized. It is made of bonded and sliding material to achieve the purpose.
(fヤ用)
前3己構成によるときは、鋳造に於けるP成分の上限値
以上のP成分を添加することができ、ネット状に析出し
たステダイトを溶体化熱処理することにより、ステダイ
トを素地に固溶させ、一部球状のステダイトを残在させ
るようにして靭性の低下を防止するようにし、限界Pv
性の向上を図った。請求項に於ける成分の限定理由はN
i : 0.2%、Cr:0.5%、 Mo: 0.0
5%以下ではFe基材料への焼入れ効果が少なく、耐摩
耗材料としては使用できない。ス、Ni:4%、Cr:
3 % +Mo:2%以上ではコストメリlトがなく
なる為である。又、C:0.8%、PEoJ%以下では
Fe−c −p系ステダイトが析出せず、又、C: 1
.4%、P : 1.0%以上では焼結時に出現するI
”e−CP液相量が多くなり過ぎ、形状を保つことがで
きなくなるためである。(For f-ya) When using the previous 3-self configuration, it is possible to add a P component exceeding the upper limit of the P component in casting, and by solution heat treating the steadite precipitated in a net shape, the steadite can be made into a base material. In order to prevent a decrease in toughness, some spherical steadite remains in the solid solution, and the limit Pv
We aimed to improve the quality of the product. The reason for limiting the ingredients in the claim is N.
i: 0.2%, Cr: 0.5%, Mo: 0.0
If it is less than 5%, the hardening effect on the Fe-based material is small and it cannot be used as a wear-resistant material. Ni: 4%, Cr:
3% +Mo: This is because if it exceeds 2%, there is no cost advantage. Moreover, if C: 0.8% and PEoJ% or less, Fe-c-p steadite does not precipitate, and C: 1
.. 4%, P: At 1.0% or more, I appears during sintering.
This is because the e-CP liquid phase amount becomes too large and the shape cannot be maintained.
(実施例)
以下、本発明の実施例について添付図面により詳述する
。(Example) Hereinafter, an example of the present invention will be described in detail with reference to the accompanying drawings.
表1の第1実施例に示す成分組成を1100℃で1時間
保持して焼結した後、950℃で1.5時間保持して溶
体化熱処理した後、さらに、600℃で1時間保持して
焼き戻し熱処理し′C得らtした焼結晶の硬度はHv3
24で、限界Pv値は6000((kg/cm”)・(
m/sec ) lであった。又、前記第1実施例と比
較するため表1に示す比較IF’llとして、成分組成
及び焼結条件を前記第1実施例と同一とし、溶体化熱処
理及び焼き戻し熱処理をしない場合の焼結晶の硬度はH
v (s 37であったが、限界Pv値がaoo。The component composition shown in Example 1 in Table 1 was held at 1100°C for 1 hour for sintering, then held at 950°C for 1.5 hours for solution heat treatment, and then held at 600°C for 1 hour. The hardness of the fired crystal obtained by tempering heat treatment is Hv3.
24, the limit Pv value is 6000 ((kg/cm”)・(
m/sec) l. In addition, as a comparison IF'll shown in Table 1 for comparison with the first example, a sintered crystal with the same component composition and sintering conditions as the first example and without solution heat treatment and tempering heat treatment was prepared. The hardness of
v (s 37, but the limit Pv value is aoo.
((kg/can’ ) 、(m/sec ) lで実
用上吊も低イ値シカ得られなかった・
第2図は比較例1による焼結晶のNi熾を示t tff
式図で、ステダイトがネット状に析出されており、球状
化されていない状態を示す図である。((kg/can'), (m/sec) l, it was not possible to obtain a low value for practical use. Figure 2 shows the nickel content of the fired crystal according to Comparative Example 1.
FIG. 2 is a diagram showing a state in which steadite is precipitated in a net shape and is not spheroidized.
次に、表1に於ける第2実施例として成分組成を第1実
施例と少し変えたものを、第1実施例と同様に溶体化熱
処理して得られた焼結晶は硬度Hv358、限界Pv値
5500(kg/cm” −m/5ec)となり第1図
は第1実施例による焼結晶の組織写真を示す図で球状化
したステダ、イトがa察される。。Next, as a second example in Table 1, the composition was slightly different from the first example, and the sintered crystal obtained by solution heat treatment in the same manner as the first example had a hardness of Hv358 and a limit of Pv. The value is 5500 (kg/cm"-m/5ec), and FIG. 1 is a photograph showing the structure of the fired crystal according to the first example, in which spheroidized spheroidal crystals can be seen.
表2
又、第2実施例と比較するために表1に示す比較例2と
して、成分組成及び焼結条件を第2実施例と同一とし、
溶体化熱処理を施さない場合の焼結晶は、硬度がHv3
09であったが限界Pv値は3000(kg/cm”
−m/5ec)で、実用上利用できない値しか得られな
かった。尚、前記限界Pv値は表2に示す条件により行
った値である。Table 2 In addition, in order to compare with the second example, as a comparative example 2 shown in Table 1, the component composition and sintering conditions were the same as the second example,
The hardness of the sintered crystal without solution heat treatment is Hv3.
09, but the limit Pv value was 3000 (kg/cm")
-m/5ec), only a value that could not be practically used was obtained. Note that the limit Pv value is a value determined under the conditions shown in Table 2.
(発明の効果)
以上詳述したよ、うに、本発明によるときは鋳造品以上
のP成分を添加することにより焼結晶に多量のステゲイ
トがネット状に析出するが、溶体化熱処理によりステダ
イトを素地に固溶させ一部球状化して残在させることが
できる。従って、多量のステダイト組織により焼結晶の
耐摩耗性が向上すると共に、ステダイトがネット状に析
出することによる靭性の低下を防止することができ、靭
性のある高耐摩耗性焼N摺動材料を得ることができる。(Effects of the Invention) As detailed above, in the case of the present invention, a large amount of stegate is precipitated in the fired crystal in the form of a net by adding more P than in the cast product, but the solution heat treatment removes the stegate from the base material. It can be made into a solid solution and left partially spheroidized. Therefore, the abrasion resistance of the sintered crystal is improved due to the large amount of steadite structure, and it is possible to prevent a decrease in toughness due to the precipitation of steadite in the form of a net. Obtainable.
第1図は本発明の第1実施例に於ける焼結晶の組織写真
を示す図、第2図は第1実施例の比較例1に於ける焼結
晶のmwLを示す模式図である・・・・ステダイト
2・・・・マルテンサイ
ト+バーライ
3・・・・空孔Fig. 1 is a diagram showing a microstructure photograph of the sintered crystal in the first example of the present invention, and Fig. 2 is a schematic diagram showing the mwL of the sintered crystal in Comparative Example 1 of the first example. ... Steadite 2 ... Martensite + Barley 3 ... Void
Claims (1)
o:0.05〜2%のうちから選ばれた1種以上を総量
で0.1〜5%含み、残部が実質的にFeから成る合金
鋼粉に、黒鉛とリン合金粉及び必要があれば純鉄粉及び
他合金粉を混合し、重量比でC:0.8〜1.4%、P
:0.6〜1.0%から成る焼結部材を焼結した後、8
50℃〜1000℃で溶体化熱処理を施し、析出したス
テダイトを球状化処理したことを特徴とする鉄系焼結摺
動材料。Weight ratio: Ni: 0.2-4%, Cr: 0.5-3%, M
o: Alloy steel powder containing one or more selected from 0.05 to 2% in a total amount of 0.1 to 5%, with the remainder substantially consisting of Fe, graphite and phosphorus alloy powder, and as necessary. If pure iron powder and other alloy powder are mixed, the weight ratio is C: 0.8 to 1.4%, P
: After sintering a sintered member consisting of 0.6 to 1.0%, 8
An iron-based sintered sliding material characterized by subjecting the precipitated steadite to spheroidization by subjecting it to solution heat treatment at 50°C to 1000°C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23558588A JPH0285338A (en) | 1988-09-20 | 1988-09-20 | Iron-based sintered sliding material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP23558588A JPH0285338A (en) | 1988-09-20 | 1988-09-20 | Iron-based sintered sliding material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0285338A true JPH0285338A (en) | 1990-03-26 |
Family
ID=16988179
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP23558588A Pending JPH0285338A (en) | 1988-09-20 | 1988-09-20 | Iron-based sintered sliding material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0285338A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7094473B2 (en) | 2002-12-27 | 2006-08-22 | Komatsu Ltd. | Wear-resistant sintered contact material, wear-resistant sintered composite contact component and method of producing the same |
| CN103008644A (en) * | 2012-11-22 | 2013-04-03 | 宁波市群星粉末冶金有限公司 | Gasoline engine piston powder metallurgical material |
| CN103008645A (en) * | 2012-11-22 | 2013-04-03 | 宁波市群星粉末冶金有限公司 | Preparation method for piston powder metallurgy material of gasoline engine |
| CN103014502A (en) * | 2012-11-22 | 2013-04-03 | 宁波市群星粉末冶金有限公司 | Powdery metallurgy material for automobile engine piston and preparation method |
| CN103357861A (en) * | 2013-06-21 | 2013-10-23 | 马鞍山市恒毅机械制造有限公司 | Powder metallurgy material of gasoline engine piston and preparation method of powder metallurgy material |
| CN112658258A (en) * | 2020-11-27 | 2021-04-16 | 无锡科宇模具有限公司 | Preparation method of copper-iron brake pad friction block |
-
1988
- 1988-09-20 JP JP23558588A patent/JPH0285338A/en active Pending
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7094473B2 (en) | 2002-12-27 | 2006-08-22 | Komatsu Ltd. | Wear-resistant sintered contact material, wear-resistant sintered composite contact component and method of producing the same |
| US7279228B2 (en) | 2002-12-27 | 2007-10-09 | Komatsu Ltd. | Wear-resistant sintered contact material, wear-resistant sintered composite contact component and method of producing the same |
| US7282078B2 (en) | 2002-12-27 | 2007-10-16 | Komatsu Ltd. | Wear-resistant sintered contact material, wear-resistant sintered composite contact component and method of producing the same |
| US7473296B2 (en) | 2002-12-27 | 2009-01-06 | Komatsu, Ltd. | Wear-resistant sintered contact material, wear-resistant sintered composite contact component and method of producing the same |
| CN103008644A (en) * | 2012-11-22 | 2013-04-03 | 宁波市群星粉末冶金有限公司 | Gasoline engine piston powder metallurgical material |
| CN103008645A (en) * | 2012-11-22 | 2013-04-03 | 宁波市群星粉末冶金有限公司 | Preparation method for piston powder metallurgy material of gasoline engine |
| CN103014502A (en) * | 2012-11-22 | 2013-04-03 | 宁波市群星粉末冶金有限公司 | Powdery metallurgy material for automobile engine piston and preparation method |
| CN103357861A (en) * | 2013-06-21 | 2013-10-23 | 马鞍山市恒毅机械制造有限公司 | Powder metallurgy material of gasoline engine piston and preparation method of powder metallurgy material |
| CN103357861B (en) * | 2013-06-21 | 2016-07-20 | 安徽吉思特智能装备有限公司 | A kind of piston powder metallurgy material of gasoline engine and preparation method thereof |
| CN112658258A (en) * | 2020-11-27 | 2021-04-16 | 无锡科宇模具有限公司 | Preparation method of copper-iron brake pad friction block |
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