JPS5823463B2 - High temperature sliding parts - Google Patents
High temperature sliding partsInfo
- Publication number
- JPS5823463B2 JPS5823463B2 JP13492976A JP13492976A JPS5823463B2 JP S5823463 B2 JPS5823463 B2 JP S5823463B2 JP 13492976 A JP13492976 A JP 13492976A JP 13492976 A JP13492976 A JP 13492976A JP S5823463 B2 JPS5823463 B2 JP S5823463B2
- Authority
- JP
- Japan
- Prior art keywords
- parts
- porosity
- melting point
- low melting
- temperature sliding
- 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
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- Powder Metallurgy (AREA)
Description
【発明の詳細な説明】
本発明は高温にて連続的又は間歇的摺動部分に使用され
る材料に関するもので例えば内燃機関、加熱炉、熱間圧
延装置等の摺動部品に広く使用される材料を提供するも
のである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a material used for continuous or intermittent sliding parts at high temperatures, and is widely used for sliding parts of internal combustion engines, heating furnaces, hot rolling equipment, etc. It provides materials.
更に具体的には内燃機関におけるバタフライバルブ軸を
支持する軸受材として好適な材料を提供しようとするも
のである。More specifically, the present invention aims to provide a material suitable as a bearing material for supporting a butterfly valve shaft in an internal combustion engine.
本軸受は排気ガスの流れをエンジン温度により変える排
気マニホールドに装入される。This bearing is installed in an exhaust manifold that changes the flow of exhaust gas depending on the engine temperature.
即ち、エンジンが冷えている時(始動時)、マニホール
ドバルブは閉じ排気ガスを吸気マニホールド経路に流す
。That is, when the engine is cold (when starting), the manifold valve closes and allows exhaust gas to flow into the intake manifold path.
この高温ガスが吸入されてきた燃料混合ガスを暖めてウ
オームアツプ時に完全な燃料の気化を生じさせるもので
ある。This high-temperature gas warms the inhaled fuel mixture gas and causes complete fuel vaporization during warm-up.
エンジンが暖まるとバタフライバルブは開き排気ガスは
定常経路で排気される。When the engine warms up, the butterfly valve opens and exhaust gas is discharged through a steady path.
排気ガス温度は約700〜800℃前後であるために、
バルブの回転シャフトと軸受表面に焼付と酸化が生じる
という問題が発生し、バルブの回転が円滑に作動しない
問題があった。Since the exhaust gas temperature is around 700-800℃,
Seizure and oxidation occurred on the surface of the valve's rotating shaft and bearing, causing the valve to not rotate smoothly.
従来、一般に使用される耐熱材料としては、溶製法によ
る超合金、ステライト合金及びステンレス鋼等があるが
、本軸受のごとき高温で間歇的に摺動する軸受には焼付
きが生じて不満足であることが判明している。Conventionally, commonly used heat-resistant materials include superalloys, stellite alloys, and stainless steels made by melting, but these are unsatisfactory because they cause seizure in bearings that slide intermittently at high temperatures, such as this bearing. It turns out that.
また従来の粉末冶金法で作られている銅系含油軸受及び
これに類似する材料では耐熱性に問題あり、使用条件に
満足しない。Furthermore, copper-based oil-impregnated bearings made by conventional powder metallurgy methods and similar materials have problems with heat resistance and do not satisfy the usage conditions.
このように高温で酸化雰囲気中で使用される間歇的摺動
材料としては、従来の耐熱合金及び軸受材料では要求を
満足できず、新しい合金の開発が必要であった。Conventional heat-resistant alloys and bearing materials cannot meet the requirements for such intermittent sliding materials used in oxidizing atmospheres at high temperatures, and it has been necessary to develop new alloys.
本発明は、このように高温軸受を初めとして汎用性のあ
る高温摺動部材としての性能を満足する安価な合金を提
供することを目的とするものであリ、以下にその内容を
述べる。The object of the present invention is thus to provide an inexpensive alloy that satisfies the performance as a versatile high-temperature sliding member, including high-temperature bearings, and its contents will be described below.
合金組成としては、重量比にてCr15〜35係、Ni
又はMn8〜40%、M o 0.1〜6 %、Cu3
〜30%、C0,1〜2%、Pb0.2〜15係及び低
融点ガラス0.5〜8係、残部Feの組成で、空孔率0
.5〜30%を有する焼結複合材である。The alloy composition is Cr15-35, Ni
Or Mn8-40%, Mo0.1-6%, Cu3
~30%, C0.1~2%, Pb 0.2~15 parts, low melting point glass 0.5~8 parts, balance Fe, porosity 0
.. 5-30%.
実施例 1
鉄粉(−100mesh)、Fe−Cr母合金粉末(−
325mesh)及び銅粉(電解)とNi粉又はフェロ
マンガン粉、モリブデン粉、グラファイト粉、鉛及び低
融点ガラス粉末を第1表に示めす組成にそれぞれ配合し
、これらの混合粉末を6t/dで成形後アンモニア分解
ガス中で1200°C焼結を行なった。Example 1 Iron powder (-100mesh), Fe-Cr master alloy powder (-
325mesh), copper powder (electrolytic), Ni powder, ferromanganese powder, molybdenum powder, graphite powder, lead, and low melting point glass powder were mixed into the composition shown in Table 1, and these mixed powders were mixed at 6t/d. After molding, sintering was performed at 1200°C in ammonia decomposition gas.
これらの焼結体の中から一部は更に窒素ガス中で100
0℃で加熱したのち加圧処理し空孔率5%以下の高密度
焼結体とした。Some of these sintered bodies were further heated to 100% in nitrogen gas.
After heating at 0° C., the material was subjected to pressure treatment to obtain a high-density sintered body with a porosity of 5% or less.
実施例 2
実施例1で配合したFe−20%Cr−10%N i
−1,5%Mo−5%Cu−1 %C−5%Pb−2係
低融点ガラス組成の混合粉末に、Co粉末及びW粉末を
添加混合して第1表に示めす組成にそれぞれ配合し、こ
れらの粉末を6t/cr?Lで成形後、アンモニア分解
ガス中で1200°C焼結を行なった。Example 2 Fe-20%Cr-10%Ni blended in Example 1
Co powder and W powder are added and mixed to the mixed powder of -1,5%Mo-5%Cu-1%C-5%Pb-2 low melting point glass composition to form the composition shown in Table 1. And these powders are 6t/cr? After molding with L, sintering was performed at 1200°C in ammonia decomposition gas.
これらの焼結体の中から一部は更に窒素ガス中で100
0°Cで加熱したのち加圧処理し空孔率5係以下の高密
度焼結体を得た。Some of these sintered bodies were further heated to 100% in nitrogen gas.
After heating at 0°C, the material was subjected to pressure treatment to obtain a high-density sintered body with a porosity of 5 or less.
実施例 3
実施例1,2にて作成した混合粉末に、低融点金属粉末
としてBi、Sb、Sn及びl’、また固体潤滑剤とし
てS2MoS2.WS2を添加混合し、前述の成形、焼
結及び熱間加圧処理を行ない、第1表に示す焼結体を得
た。Example 3 To the mixed powder prepared in Examples 1 and 2, Bi, Sb, Sn, and l' were added as low melting point metal powders, and S2MoS2. WS2 was added and mixed, and the above-described molding, sintering, and hot pressing treatments were performed to obtain the sintered bodies shown in Table 1.
斯くして得た焼結体のうち第2表に示す試料7種及び比
較材については、軸受形状に加工し、バタフライバルブ
の開閉実験を行った。Of the sintered bodies thus obtained, the seven types of samples shown in Table 2 and the comparative material were processed into a bearing shape, and an opening/closing experiment of a butterfly valve was conducted.
実験条件は下記の通りである。The experimental conditions are as follows.
(1)軸受形状=10φ×6φX25mm(2)バタフ
ライシャフト材質ニ
オーステナイト系ステンレス
(3)よう動角度:0〜100゜
(4)よう動速度:3同/ rn 1 n(5)加熱サ
イクル:
図面に示す通り
但し、A=0.5Hr
B=2Hr
C=0.5Hr
D=1.0Hr
(6)雰囲気=10係H20気中
(7)ハウジング:鋳鉄
スムーズな作動が困難になった時点(よう動トルクが1
0kgvtm以上に相当)をもって耐久時間とした。(1) Bearing shape = 10φ x 6φ x 25mm (2) Butterfly shaft material: Niostenitic stainless steel (3) Swivel angle: 0 to 100° (4) Swivel speed: 3/rn 1 n (5) Heating cycle: Drawing However, as shown in , A = 0.5 Hr B = 2 Hr C = 0.5 Hr D = 1.0 Hr (6) Atmosphere = 10 ratio H20 air (7) Housing: Cast iron When smooth operation becomes difficult ( dynamic torque is 1
(equivalent to 0 kgvtm or more) was taken as the durability time.
この耐久実験の結果を第2表に示す。比較材の硬さ
316ステンレス RB80〜90
ニレジスト 80〜90
焼結材(I) 75〜85これらの結
果から明らかな様に本発明材は苛酷な摺動条件にも拘ら
ず焼付き現象が生じなかった。The results of this durability experiment are shown in Table 2. Hardness of comparison materials: 316 Stainless steel RB80-90 Niresist 80-90 Sintered material (I) 75-85 As is clear from these results, the invention material did not cause seizure despite severe sliding conditions. Ta.
次に本発明部材の構成元素の機能と組成について説明す
る。Next, the functions and compositions of the constituent elements of the member of the present invention will be explained.
Ni又はMn:8〜40係 鉄中に固溶しオーステナイト化を促進する。Ni or Mn: 8-40 section It forms a solid solution in iron and promotes austenitization.
8係以下ではオーステナイト化が不十分、40係を超え
ると効果はなく、価格が高くなる。If the ratio is less than 8, the austenitization is insufficient, and if it exceeds 40, there is no effect and the price becomes high.
Mo:0.1〜6係
7トリツクスに固溶し耐熱性、耐酸化性を改善するが、
0.1係以下では効果不十分、6%以上では脆化する。Mo: 0.1 to 6 and 7 solid solution in Trix to improve heat resistance and oxidation resistance,
If it is less than 0.1%, the effect is insufficient, and if it is more than 6%, it becomes brittle.
Cu:3〜30係
鉄中に固溶し耐食性改善に役立つ他、未固溶の銅は摺動
中に酸化銅となって耐焼き付き性の改善に寄与し、又熱
伝導性を高めて放熱性、熱膨張係数の調整に役立つが、
3係以下では効果が小さく、30係以上となっては強度
低下が大きくなる。Cu: 3 to 30 In addition to being solid dissolved in the steel and helping to improve corrosion resistance, undissolved copper turns into copper oxide during sliding, contributing to improving seizure resistance, and also improves thermal conductivity and dissipates heat. It is useful for adjusting the properties and coefficient of thermal expansion.
When the ratio is 3 or less, the effect is small, and when it is 30 or more, the strength decreases greatly.
C:0.2〜2係
鉄中に同容してマトリックスの強度を改善すると同時に
炭化物を形成し耐摩性の改善に寄与するが、0.2係以
下では不十分で、2係以上となっては網状の炭化物量が
増し却って強度が低下する。C: 0.2 to 2 C is incorporated in iron to improve the strength of the matrix and at the same time forms carbides, contributing to the improvement of wear resistance, but if it is less than 0.2, it is insufficient, and if it is more than In this case, the amount of net-like carbide increases and the strength decreases.
Pb:0.2〜15係
マ) IJラックス固溶せず、焼結体の空隙内に収まっ
て存在する常温から300〜400°Cの温度範囲で潤
滑成分として作用し焼付きを防止する。Pb: 0.2 to 15%) IJ Lux does not form a solid solution and acts as a lubricating component in the temperature range from room temperature to 300 to 400°C where it exists within the voids of the sintered body and prevents seizure.
0.2係以下では効果なく、15係以上となると強度低
下が大きくなる。If the ratio is less than 0.2, there is no effect, and if it is more than 15, the strength will decrease significantly.
ガラス二0.5〜8係
P2O5、B2O3,PbO、K2O、Na2Oを主構
成成分とし、300℃前後に軟化点を有する低融点ガラ
ス。A low-melting glass whose main constituents are P2O5, B2O3, PbO, K2O, and Na2O and has a softening point around 300°C.
300°C以上の温度域で潤滑成分として作用するが、
0.5係以下では潤滑機能不十分、8係以上となると強
度低下が大きくなる。It acts as a lubricating component in the temperature range of 300°C or higher, but
If the ratio is less than 0.5, the lubrication function is insufficient, and if it is more than 8, the strength will be significantly reduced.
Co:1〜15係
マトリックス中に固溶し耐熱性の改善に寄与するが、1
係以下では効果が小さく、15係以上では強度低下が大
きくなる。Co: 1 to 15 Co dissolves solidly in the matrix and contributes to improving heat resistance;
If the ratio is less than 15, the effect will be small, and if it is 15 or more, the strength will decrease significantly.
Cr :W: 1〜15%
マトリックス中に固溶し耐熱性、耐酸化性を改善すると
同時に一部耐摩耗性改善に役立つが、1係以下では、こ
れらの効果が小さく、15%以上になると加工性が著し
く低下する。Cr:W: 1 to 15% Solid solution in the matrix improves heat resistance and oxidation resistance, and at the same time helps to partially improve wear resistance, but below 1%, these effects are small, and above 15% Workability is significantly reduced.
なお、本発明材料の多孔率は0.5〜30係の範囲が適
当である。The porosity of the material of the present invention is suitably in the range of 0.5 to 30.
即ち高温摺動時に生じた酸化物及び周囲の雰囲気からデ
ポジットした異物が摺動面に付着した場合、表面空孔部
にこれらの付着物を埋め込ませて、アブレツシブ摩耗を
防止させ、逆にCu、Pb、Mo等の酸化物は耐焼付性
に効果がある。That is, when oxides generated during high-temperature sliding and foreign matter deposited from the surrounding atmosphere adhere to the sliding surface, these deposits are buried in the surface pores to prevent abrasive wear. Oxides such as Pb and Mo are effective in improving seizure resistance.
空孔率が0.5以下では効果がなく、30係以上では材
料の強度低下が大となる。If the porosity is less than 0.5, there is no effect, and if the porosity is more than 30, the strength of the material will decrease significantly.
尚、実施例においては粉末混合法によるものについて示
したが、例えばCu、Pbガラス及び固体潤滑材等は含
浸して添加しても勿論差支えない。In the examples, the powder mixing method was used, but it goes without saying that Cu, Pb glass, solid lubricants, etc. may be impregnated and added.
図面は本発明部材の耐久実験における加熱サイクルの条
件を示す図表である。The drawing is a chart showing heating cycle conditions in durability tests of members of the present invention.
Claims (1)
0係、Mo0.1〜6%、Cu3〜30%、C0,1〜
2係、Pb0.2〜15係、及び低融点ガラス0.5〜
8係、残部Feの組成で、空孔率0.5〜30係を有す
る焼結複合材からなる高温摺動部材。 2 重量比にてCr15〜35%、Ni又はMn8〜4
0%、Mo0.1〜6%、Cu3〜30%、C0,1〜
2係、Pb0.2〜15係、低融点ガラス0.5〜8%
、及びCo 、Wの1種又は2種1〜15係、残部Fe
の組成で、空孔率0.5〜30係を有する焼結複合材か
らなる高温摺動部材。 3 重量比にてCr15〜35%、Ni又はMn8〜4
0%、Mo0.1〜6%、Cu3〜30係、C061〜
2係、Pb0.2〜15係、低融点ガラス0.5〜8係
、及びAg又は低融点金属のBi。 Sb 、Snの1種又は2種以上0.5〜5%、残部F
eの組成で、空孔率0.5〜30係を有する焼結複合材
からなる高温摺動部材。 4 重量比にてCr15〜35%、Ni又はMn8〜4
0係、Mo0.1〜6%、Cu3〜30%、co、i〜
2係、PbO,2〜15係、低融点ガラス0.5〜8%
、及び固体潤滑剤として、S 、MoS2 。 WS2の1種又は2種以上0..5〜5 %、残部Fe
の組成で、空孔率0.5〜30係を有する焼結複合材か
らなる高温摺動部材。[Claims] 1 Cr: 15-35%, Ni or Mn: 8-4% by weight
0 ratio, Mo0.1-6%, Cu3-30%, C0.1-
2 parts, Pb 0.2~15 parts, and low melting point glass 0.5~
A high-temperature sliding member made of a sintered composite material having a composition of 8 parts, the balance being Fe, and a porosity of 0.5 to 30 parts. 2 Cr15-35%, Ni or Mn8-4 in weight ratio
0%, Mo0.1-6%, Cu3-30%, C0.1-
2 parts, Pb 0.2 to 15 parts, low melting point glass 0.5 to 8%
, and Co, one or two types 1 to 15 of W, the remainder Fe
A high-temperature sliding member made of a sintered composite material having a composition of 0.5 to 30 and a porosity of 0.5 to 30. 3 Cr15-35%, Ni or Mn8-4 in weight ratio
0%, Mo0.1-6%, Cu3-30, C061-
2 parts, Pb 0.2 to 15 parts, low melting point glass 0.5 to 8 parts, and Bi of Ag or low melting point metal. 0.5-5% of one or more of Sb and Sn, balance F
A high-temperature sliding member made of a sintered composite material having a composition of e and a porosity of 0.5 to 30. 4 Cr15-35%, Ni or Mn8-4 in weight ratio
0 ratio, Mo0.1~6%, Cu3~30%, co, i~
2 parts, PbO, 2 to 15 parts, low melting point glass 0.5 to 8%
, and S, MoS2 as solid lubricants. One or more types of WS2 0. .. 5-5%, balance Fe
A high-temperature sliding member made of a sintered composite material having a composition of 0.5 to 30 and a porosity of 0.5 to 30.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13492976A JPS5823463B2 (en) | 1976-11-10 | 1976-11-10 | High temperature sliding parts |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP13492976A JPS5823463B2 (en) | 1976-11-10 | 1976-11-10 | High temperature sliding parts |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5360306A JPS5360306A (en) | 1978-05-30 |
| JPS5823463B2 true JPS5823463B2 (en) | 1983-05-16 |
Family
ID=15139842
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP13492976A Expired JPS5823463B2 (en) | 1976-11-10 | 1976-11-10 | High temperature sliding parts |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5823463B2 (en) |
-
1976
- 1976-11-10 JP JP13492976A patent/JPS5823463B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5360306A (en) | 1978-05-30 |
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