JPS62177159A - Sintered alloy member having excellent wear resistance - Google Patents

Sintered alloy member having excellent wear resistance

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Publication number
JPS62177159A
JPS62177159A JP1995286A JP1995286A JPS62177159A JP S62177159 A JPS62177159 A JP S62177159A JP 1995286 A JP1995286 A JP 1995286A JP 1995286 A JP1995286 A JP 1995286A JP S62177159 A JPS62177159 A JP S62177159A
Authority
JP
Japan
Prior art keywords
sintered alloy
wear resistance
carbide
hardness
alloy member
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
Application number
JP1995286A
Other languages
Japanese (ja)
Inventor
Shigezo Osaki
茂三 大崎
Sumio Jinno
神野 純夫
Tsuyoshi Morishita
強 森下
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.)
Mazda Motor Corp
Original Assignee
Mazda Motor Corp
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 Mazda Motor Corp filed Critical Mazda Motor Corp
Priority to JP1995286A priority Critical patent/JPS62177159A/en
Publication of JPS62177159A publication Critical patent/JPS62177159A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To obtain a sintered alloy member having excellent wear resistance, hardness and toughness by uniformly dispersing fine carbide such as Cr3C2 having high hardness into a sintered alloy matrix made of a specific compsn. consisting of C, Cr, P, Mo, B and Fe. CONSTITUTION:The carbide such as Cr3C2, NbC, TaC, TiC, WC, VC, ZrC or HfC which has <=10mu average grain size, has about >=1,300 Hv hardness and does not decompose at a sintering temp. of about 1,000-1,130 deg.C is dispersed into the sintered alloy matrix which contains 1.0-4.0wt% C, 4.0-7.0% Cr and least one kind of 0.5-2.0% P, 2.0-6.0% Mo and 0.5-3.0% B and consists of the balance Fe and unavoidable components. The sintered alloy member having the sorbite structure which is excellent in the wear resistance, hardness and toughness is thus obtd. The above-mentioned member can be made into a sliding member having an excellent sliding characteristic by forming fine oil holding recesses on the surface with good dispersibility by buffing, etc.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、高血圧のかかる摺動部材として用いられ、耐
摩耗性において優れるとともに、相手部材をH1傷しな
い焼結合金flll材に関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a sintered alloy full material that is used as a sliding member subject to high blood pressure, has excellent wear resistance, and does not cause H1 damage to a mating member.

(従来の技術) 近年、車両の高速化および高出力化に伴い、内燃機関の
動弁系部材、特に高面圧のかかるロッカアームバット面
、カム、スリーブ、およびバルブシートなどに対する耐
摩耗性、耐スカッフィング性、および耐ピツチング性に
関する要求はきわめて厳しくなりつつあり、しかもこの
場合相手部組をも千員傷しないものでなければならない
(Prior Art) In recent years, with the increase in speed and output of vehicles, the wear resistance and resistance of internal combustion engine valve train members, especially rocker arm butt surfaces, cams, sleeves, and valve seats, which are subject to high surface pressure, has increased. Requirements regarding scuffing resistance and pitting resistance are becoming extremely strict, and in this case, it is also necessary to avoid damaging the mating assembly.

このような高面圧のかかる摺動部材に適用される焼結合
金部材として、従来、液相焼結法により、焼結合金マト
リックス中にNbC等の高硬度の炭化物を析出させ、分
散させたものが提案されている(特公昭60−3318
1号公報参照)。しかしながら、該焼結合金部材では、
炭化物が粗大化し易く、耐摩耗性の向上を妨げるという
問題点があった。
Conventionally, high hardness carbides such as NbC are precipitated and dispersed in a sintered alloy matrix using liquid phase sintering to produce sintered alloy members that are applied to sliding members that are subject to high surface pressure. (Special Publication No. 60-3318)
(See Publication No. 1). However, in this sintered alloy member,
There was a problem in that carbides tend to become coarse, which hinders improvement in wear resistance.

そこで、予め用意したNbC等の炭化物の粒子を合金粉
末に混ぜた後、焼結を行うようにしたものが特開昭59
−118859号公報において提案されている。
Therefore, in JP-A-59, a method was developed in which pre-prepared carbide particles such as NbC were mixed with alloy powder and then sintered.
This is proposed in Japanese Patent No.-118859.

しかし、従来の焼結合金fall拐では、耐摩耗性に関
連する炭化物の粒径において、なお改善の余地を残すと
ともに、焼結合金マトリックスにNiが含有されること
から、残留オーステナイトが存在して、軟らかく、かつ
強度的にも弱いという問題、Wがあった。
However, in conventional sintered alloy fall grinding, there is still room for improvement in the grain size of carbides related to wear resistance, and since Ni is contained in the sintered alloy matrix, residual austenite is present. , W had the problem of being soft and having low strength.

また、パフ研摩または化学エツチングにより、焼結合金
部材の表面を凹凸化した際に形成される凹部は微細化さ
れておらず、オイル保持四部としては適さないという問
題点もあった。
Another problem is that the recesses that are formed when the surface of the sintered metal member is roughened by puff polishing or chemical etching are not miniaturized, making them unsuitable for use as oil retaining parts.

(発明の目的) 本発明は、前記従来の問題点に鑑みなされたもので、微
細な高硬度の炭化物が均一に分散して耐摩耗性において
優れるとともに、組織がソルバイト組織であって硬さお
よび靭性においても優れた焼結合金部材を提供すること
を目的とする。
(Object of the Invention) The present invention has been made in view of the above-mentioned conventional problems, and has excellent wear resistance by uniformly dispersing fine, high-hardness carbides, and has a sorbite structure that improves hardness and The object is to provide a sintered alloy member that is also excellent in toughness.

本発明の他の目的は、パフ研摩または化学エツチングに
より、微細なオイル保持凹部が分散性良く形成される焼
結合金部材を提供することを目的とする。
Another object of the present invention is to provide a sintered alloy member in which fine oil retaining recesses are formed with good dispersion by puff polishing or chemical etching.

(発明の構成)゛ 前記目的を達成するために、本発明の耐摩耗性に優れた
焼結合金部材は、重量比でC・1.0〜4.0%、 C
r : 4.0〜7.0%、およびP:0.5〜2.0
%。
(Structure of the Invention) ``In order to achieve the above object, the sintered alloy member of the present invention having excellent wear resistance has a weight ratio of 1.0 to 4.0% C.
r: 4.0-7.0%, and P: 0.5-2.0
%.

M O: 2.0−6.0%、  B :0.5〜3.
0%のうちの少なくとも一種を含有し、残部がFeおよ
び不可避成分からなる焼結合金マトリックスに、平均粒
径が10μ以下であるCr3C2、NbC,TaC,T
iC,WC,VC,ZrC,HfCのうち少なくとも一
種の炭化物を分散したソルバイト組織を有することを特
徴としている。
MO: 2.0-6.0%, B: 0.5-3.
Cr3C2, NbC, TaC, T having an average particle size of 10μ or less in a sintered alloy matrix containing at least one of 0% and the remainder consisting of Fe and unavoidable components.
It is characterized by having a sorbite structure in which at least one type of carbide among iC, WC, VC, ZrC, and HfC is dispersed.

以下、本発明において組成を上記の通りに限定した理由
を述べる。
The reason why the composition is limited as described above in the present invention will be described below.

(a) C C成分には、焼結合金マトリックス中に固溶してこれを
強化し、かつFeおよびP、Mo、Bの少なくとも一種
とともに低融点の三元集品を形成して液相を発生させ、
焼結合金部材を緻密化させる作用がある。その含有量が
1.0%未満の場合は、液相量が不足するため、焼結密
度が7.0 g /cff!未満となることからもわか
るように気孔が多くなり、耐摩耗性が低下する。また、
含有量が4.0%を越えると、液相量が過多になって、
焼結時に変形を招くとともに、炭化物量が多くなり、脆
くなる。
(a) The C component is solid-dissolved in the sintered alloy matrix to strengthen it, and forms a low melting point ternary collection with Fe and at least one of P, Mo, and B to form a liquid phase. generate,
It has the effect of making the sintered alloy member denser. If the content is less than 1.0%, the amount of liquid phase is insufficient, so the sintered density is 7.0 g/cff! As can be seen from the fact that it is less than 100%, the number of pores increases and the abrasion resistance decreases. Also,
When the content exceeds 4.0%, the amount of liquid phase becomes excessive,
In addition to causing deformation during sintering, the amount of carbides increases and becomes brittle.

したがって、Cの含有量は1.0〜4.0%が好ましい
Therefore, the C content is preferably 1.0 to 4.0%.

(b)Cr Cr成分は、焼結合金マトリックスに固溶し、強度を高
め、またCと結合してCr炭化物を形成し耐摩耗性を向
上させる。その焼結合金マトリックス中の含有量が4.
0%未満では所望する耐摩耗性を得ることができず、7
.0%を越えると炭化物が粗大化し靭性を低下させる傾
向があるので、これを越えてはならない。したがって、
Crの含有量は4.0〜7.0%が好ましい。
(b) Cr The Cr component solidly dissolves in the sintered alloy matrix to increase strength, and also combines with C to form Cr carbide to improve wear resistance. The content in the sintered alloy matrix is 4.
If it is less than 0%, the desired wear resistance cannot be obtained;
.. If it exceeds 0%, the carbides tend to become coarse and the toughness decreases, so it should not be exceeded. therefore,
The content of Cr is preferably 4.0 to 7.0%.

(c)P、Mo、B P、Mo、Bは、何れもFe、 cとともに三元集品を
形成して焼結中に液相させ、焼結体の緻密化に寄与する
。しかし、その含有量が、Pの場合は0.5%未満、M
oの場合は2.0%未満、Bの場合は0.5%未満のと
きは、液相量が不足して摩耗量の急激な増加を招く。ま
た、その含有量が、Pの場合は2.0%、Moの場合は
6.0%、Bの場合は3.0%を越えるときは、液相量
が過多になり、焼結合金部材の焼結時における変化およ
び脆化を招く。したがって、Pの含有量は0.5〜2.
0%、M。
(c) P, Mo, B P, Mo, and B all form a ternary assembly together with Fe and c, are brought into a liquid phase during sintering, and contribute to the densification of the sintered body. However, the content is less than 0.5% in the case of P, M
If it is less than 2.0% in the case of o, and less than 0.5% in the case of B, the amount of liquid phase will be insufficient, leading to a rapid increase in the amount of wear. In addition, when the content exceeds 2.0% for P, 6.0% for Mo, and 3.0% for B, the amount of liquid phase becomes excessive and the sintered alloy member This leads to changes and embrittlement during sintering. Therefore, the P content is between 0.5 and 2.
0%, M.

の含有量は2.0〜6.0%、Bの含有量は0.5〜3
.0%であることが好ましい。
The content of B is 2.0 to 6.0%, and the content of B is 0.5 to 3.
.. Preferably it is 0%.

(d)CrlCIl NbC,TaC,Tic、wc。(d) CrlCIl NbC, TaC, Tic, wc.

VC,ZrC,Hfに れらの炭化物は何れもHv1300以上の高硬度を有す
るので、焼結合金マトリックス中に分散させることによ
り、耐摩耗性の向上が可能である。
Since carbides such as VC, ZrC, and Hf all have high hardness of Hv1300 or more, it is possible to improve wear resistance by dispersing them in the sintered alloy matrix.

前記炭化物の平均粒径が10μ以下であることが好まし
いのは、次の理由に基づく。すなわち、平均粒径が10
μを越すと、炭化物は焼結合金マトリックス中で粗大化
し易く、かつ分散性も悪くなるので、相手部材を損傷す
る虞があるとともに、炭化物が粗大化すると、該炭化物
を保持する焼結合金マトリックスが減少するので、該焼
結合金部材を適用した摺動部材を使用した際に炭化物が
脱落し易く、摺動特性が劣化するからである。さらに、
炭化物の分散性が悪いと、該焼結合金部材の表面にパフ
研摩等を施しても、油膜形成に都合のよい分散性の良好
なオイル保持四部が形成され難くなるからである。
The reason why the average particle size of the carbide is preferably 10 μm or less is based on the following reason. That is, the average particle size is 10
If μ is exceeded, the carbide tends to become coarse in the sintered alloy matrix and the dispersibility becomes poor, so there is a risk of damaging the mating member, and if the carbide becomes coarse, the sintered alloy matrix that holds the carbide This is because when a sliding member to which the sintered alloy member is applied is used, the carbide tends to fall off and the sliding properties deteriorate. moreover,
This is because if the dispersibility of the carbide is poor, even if the surface of the sintered alloy member is subjected to puff polishing or the like, it will be difficult to form oil retaining portions with good dispersibility that are convenient for forming an oil film.

なお、高硬度を有する炭化物のうちでも、前記Cr、C
,等が好ましいのは、次の理由に基づく。
Furthermore, among the carbides having high hardness, the above-mentioned Cr, C
, etc. are preferable for the following reasons.

すなわち、前記Cr、C2等の炭化物は、1000〜1
130℃の焼結温度で熱分解せず、添加した際の粒径の
ままで焼結合金マトリックス中に存在するからである。
That is, the carbides such as Cr and C2 have a content of 1000 to 1
This is because it does not thermally decompose at the sintering temperature of 130° C. and remains in the sintered alloy matrix with the same particle size as when it was added.

これに対し、例えばMoCのように、上記焼結温度で熱
分解する炭化物は、分解後に再結晶する際に粗大化して
、平均粒径が10μを越えた場合と同様の弊害をもたら
すので、本発明においては好ましくない。
On the other hand, carbides such as MoC, which are thermally decomposed at the above sintering temperature, become coarse when recrystallized after decomposition, causing the same problems as when the average particle size exceeds 10 μm. This is not preferable in terms of invention.

(実施例) 以下、本発明による焼結合金部材を摺動部材に適用した
具体的な実施例について説明する。
(Example) Hereinafter, a specific example in which the sintered alloy member according to the present invention is applied to a sliding member will be described.

本発明の焼結合金部材を摺動部材として適したものにす
るには、Fe−P(またはMo、B)−Cの共晶合金粉
末と5OS410合金粉末および硬さHv 1300以
上、粒径10μ以下、さらに焼結温度1000〜113
0’cの範囲で熱分解しない炭化物粉(Cr3C2、N
bC,TaC,TiC。
In order to make the sintered alloy member of the present invention suitable as a sliding member, it is necessary to use a Fe-P (or Mo, B)-C eutectic alloy powder, a 5OS410 alloy powder, a hardness of Hv 1300 or more, and a particle size of 10μ. Below, the sintering temperature is 1000 to 113
Carbide powder (Cr3C2, N
bC, TaC, TiC.

WC,VC,Zr、C,HfC)からなる焼結合金部材
の摺動面をパフ研摩加工または化学エツチング処理し、
表面の組織中のマトリックスを優先的に研摩もしくはエ
ツチングすることにより、摺動面を凹凸化させ、表面粗
さをRmax 1.0〜3,0μとし、該摺動面の凹部
をもって容易にオイル保持凹部となすことのできる焼結
合金部材を製造する。
Puff polishing or chemical etching is applied to the sliding surface of a sintered alloy member made of WC, VC, Zr, C, HfC,
By preferentially polishing or etching the matrix in the surface structure, the sliding surface is made uneven, with a surface roughness of Rmax 1.0 to 3.0μ, and the recesses on the sliding surface make it easy to retain oil. A sintered metal member that can be formed into a recess is manufactured.

前記炭化物の硬さをHv1300以上としたのは、Hv
1300未満では、所望の優れた耐摩耗性が得られず、
また、パフ研摩にて炭化物が研摩され易いため、摺動面
の凹凸化が難しくなるからである。パフ研摩または化学
エツチングにより凹凸化した摺動面の表面粗さがRma
xl、Oμ未満では十分なオイル溜め作用が望めず、R
max3.0μを越えると相手部材を損傷する虞がある
ため、表面粗さはRmax 1.0〜3.0μの範囲が
良い。
The hardness of the carbide is set to Hv1300 or more because Hv
If it is less than 1300, the desired excellent wear resistance cannot be obtained,
Further, since carbide is easily polished by puff polishing, it becomes difficult to make the sliding surface uneven. The surface roughness of the sliding surface made uneven by puff polishing or chemical etching is Rma
If it is less than xl or Oμ, a sufficient oil reservoir effect cannot be expected, and R
If Rmax exceeds 3.0μ, there is a risk of damaging the mating member, so the surface roughness is preferably in the range of Rmax 1.0 to 3.0μ.

次に、より具体的な実施例について説明する。Next, a more specific example will be described.

〈実施例1〉 C: 1.94重量%、P : 1.12重量%、M 
o : 4.78重量%、Crニア、95重量%、残部
Feからなる粒径150メツシユ以下の耐摩耗性共晶合
金粉末90重量%と粉末粒径1.1μのNbC粉末10
重量%を混合してなる混合粉末97容量%と、トルエン
で溶いたアクリル樹脂3容量%とを混練した後、厚さ1
.5mmにシート化し、幅16.5mm、長さ18.5
mmにカットし、チップ材(鋼材)にアクリル樹脂系の
接竹剤で接着後、水素雰囲気中でlO℃/分の昇温速度
で300℃まで加熱昇温し、その温度に60分間保持し
て予備焼結を行った。次に、これを真空炉で10℃/分
の昇温速度で1100℃まで加熱昇温し、その温度に2
0分間保持した後、900℃まで降温し、この温度に3
0分間保持した後、 N2ガスにて焼入れを行う。次に
、560℃の真空炉に100分間保持して焼戻しを行う
ことにより、ロックウェルC硬度59のtt%結合金部
拐が得られた。
<Example 1> C: 1.94% by weight, P: 1.12% by weight, M
o: 90% by weight of wear-resistant eutectic alloy powder with a particle size of 150 mesh or less consisting of 4.78% by weight, near Cr, 95% by weight and the balance Fe, and NbC powder 10 with a powder particle size of 1.1μ
After kneading 97% by volume of mixed powder obtained by mixing % by weight with 3% by volume of acrylic resin dissolved in toluene,
.. 5mm sheet, width 16.5mm, length 18.5mm
After cutting the pieces into 1/4 inch pieces and adhering them to a chip material (steel material) using an acrylic resin-based grafting agent, the pieces were heated to 300°C at a heating rate of 10°C/min in a hydrogen atmosphere and held at that temperature for 60 minutes. Preliminary sintering was performed. Next, this was heated to 1100°C in a vacuum furnace at a heating rate of 10°C/min, and the temperature was increased to 2
After holding for 0 minutes, the temperature was lowered to 900℃, and the temperature was kept at this temperature for 3
After holding for 0 minutes, harden with N2 gas. Next, by holding it in a vacuum furnace at 560° C. for 100 minutes and tempering it, a tt% alloy flake having a Rockwell C hardness of 59 was obtained.

この焼結合金部材をAQダイカストにて鋳ぐるむことに
より、AQロッカアームを得た。次に、このAf1ロッ
カアームを機械加工し、摺動面を研削加工後、研摩剤青
棒にてパフ研摩することにより、表面が凹凸化し、表面
粗さRmax 1.2〜2.1μのAQロッカアームが
得られた。
An AQ rocker arm was obtained by casting this sintered metal member using AQ die casting. Next, this Af1 rocker arm is machined, and after grinding the sliding surface, it is puff-polished with an abrasive blue rod to make the surface uneven, and the AQ rocker arm has a surface roughness Rmax of 1.2 to 2.1μ. was gotten.

第1図はこのようにして製造された本発明例のロッカア
ーム1を図示したもので、鋼材よりなるチップ材2の底
部に、摺動部材として、本発明による焼結合金部材3が
接着されている。該焼結合金部材3の表面にパフ研摩が
施され、カム部材と摺動する摺動面4が形成されている
FIG. 1 shows a rocker arm 1 according to an example of the present invention manufactured in this manner, in which a sintered alloy member 3 according to the present invention is bonded as a sliding member to the bottom of a chip material 2 made of steel. There is. Puff polishing is applied to the surface of the sintered metal member 3 to form a sliding surface 4 that slides on the cam member.

次に、このAQロッカアーム1をエンジンに組込み、摺
動特性をモータリング法にて評価した。
Next, this AQ rocker arm 1 was assembled into an engine, and its sliding characteristics were evaluated by the motoring method.

テスト条件は以下の通りである。The test conditions are as follows.

エンジン回転数×テスト時間: 2000rpmX100Hr 潤滑油: 商品名〔出先アポロブイーゼル5AZ30#];渭滑油
温度:50℃ スプリングセット荷重:34kg 相手部材・タフトライド処理したチル合金鋳鉄製カムシ
ャフト さらに、本発明例の焼結合金部材3の代りに、組成が重
量比でC:2.4%、Cr:11.3%、M。
Engine rotation speed x test time: 2000 rpm x 100 Hr Lubricating oil: Product name [Department Apollo Bueasel 5AZ30#]; Wei lubricating oil temperature: 50°C Spring set load: 34 kg Mating member: Chill alloy cast iron camshaft treated with Tuftride Furthermore, the present invention example Instead of the sintered alloy member 3, the composition is C: 2.4%, Cr: 11.3%, M in weight ratio.

:1.8%、残部Feの焼結合金部材を用いた従来例の
ロッカアームについて、上記と同一の条件でテストを行
った。これら本発明例および従来例についてのテスト結
果を下記第1表に示す。数値は何れも摩耗量であって、
()の外が平均値、()の中が最小値および最大値であ
る。
A conventional rocker arm using a sintered alloy member having: 1.8% and the balance Fe was tested under the same conditions as above. Test results for these examples of the present invention and conventional examples are shown in Table 1 below. All numbers are the amount of wear,
The values outside the parentheses are the average value, and the values inside the parentheses are the minimum and maximum values.

第  1  表 上記テスト結果から明らかなように、本発明例において
は、摺動部材の摩耗量は−に、また相平部材の摩耗量は
約半分に減少し、摺動特性の著しい向上が達成される。
Table 1 As is clear from the above test results, in the example of the present invention, the amount of wear on the sliding member was reduced to -, and the amount of wear on the opposing member was reduced by about half, achieving a significant improvement in the sliding characteristics. be done.

次に、第2図ないし第4図の写真(倍率400)により
、焼結合金部材の組織について説明する。
Next, the structure of the sintered alloy member will be explained using the photographs (magnification: 400) shown in FIGS. 2 to 4.

第2図はテストに用いた従来例についての写真である。FIG. 2 is a photograph of the conventional example used in the test.

マトリックスはベイナイト組織であり、棒状または粒状
白色部はOrの炭化物またはCr−Moの複合炭化物か
らなる。
The matrix is a bainite structure, and the rod-like or granular white parts are made of Or carbide or Cr-Mo composite carbide.

第3図は比較例として、NbCを分散させない一方、そ
の他については本発明のものと同一の条件で製造した焼
結合金部材の組織を示す。マトリックスはソルバイト組
織であるが、白色部はCrの炭化物またはCr−Moの
複合炭化物からなる。
FIG. 3 shows, as a comparative example, the structure of a sintered alloy member manufactured under the same conditions as those of the present invention but without dispersing NbC. The matrix is a sorbite structure, and the white part is made of Cr carbide or Cr-Mo composite carbide.

第4図はテストに用いた本発明例(実施例1)について
の写真である。マトリックスはソルバイト組織である。
FIG. 4 is a photograph of an example of the present invention (Example 1) used in the test. The matrix is a sorbite tissue.

そして、従来例および比較例と異なり、マトリックスと
白色部の境界に綿状白色部が形成されている。該綿状白
色部はNbCからなる。また、白色部は、Crの炭化物
とNbCまたはCr−Moの複合炭化物からなることが
確かめられている。
Unlike the conventional example and the comparative example, a cottony white part is formed at the boundary between the matrix and the white part. The flocculent white part consists of NbC. Furthermore, it has been confirmed that the white portion is composed of a Cr carbide and a composite carbide of NbC or Cr-Mo.

このように、微細なNbCが均一に分散しているので、
焼結合金部材に優れた耐摩耗性がもたらされる。また、
組織がソルバイト組織であるので、高硬度および優れた
靭性がもたらされる。
In this way, fine NbC is uniformly dispersed, so
Excellent wear resistance is provided to the sintered alloy member. Also,
Since the structure is a sorbite structure, high hardness and excellent toughness are provided.

次に、第5図、第6図の写真により、前記従来例および
本発明例の焼結合金部材をパフ研摩した後の摺動面につ
いて説明する。写真は何れも走査型電子顕微鏡により、
倍率1000で撮影したものである。
Next, referring to the photographs shown in FIGS. 5 and 6, the sliding surfaces of the sintered alloy members of the conventional example and the example of the present invention after being puff-polished will be described. All photographs were taken using a scanning electron microscope.
This photo was taken at a magnification of 1000.

第5図は従来例についての写真である。色の濃い部分が
凸部、htJ、い部分が凹部である。写真の通り、形成
される四部が極めて大きいため、該凹部にはオイル溜め
作用が乏しい。
FIG. 5 is a photograph of a conventional example. The dark colored parts are convex parts, htJ, and dark colored parts are concave parts. As shown in the photo, since the four parts formed are extremely large, the recesses have poor oil storage function.

これに対して第6図の写真に示す本発明例のものは、写
真の通り微細な凹部が分散した状態で存在するので、該
凹部がオイル保持凹部として有効に作用する。前記テス
トにおいて、本発明例のロッカアームの方が従来例のも
のより良い摺動特性が得られたのは、このような凹部の
構造の違いに基づく。
On the other hand, in the example of the present invention shown in the photograph of FIG. 6, fine recesses are present in a dispersed state as shown in the photograph, so that the recesses effectively act as oil retaining recesses. The reason why the rocker arm of the present invention had better sliding characteristics than the conventional example in the above test is due to the difference in the structure of the recess.

〈実施例2〉 実施例1と同じ組成の対摩純性共品合金粉末83重量%
と粒径1.5μのTaC粉末17重量%を混合した混合
粉末に、アセトンで稀釈したしょうのう2重量%を加え
て混練した後、プレス圧6.0ton/−で圧粉体のチ
ップを成形した。次にこの圧粉体チップを600℃の水
素雰囲気中で予備焼結後、1120’cの真空炉に20
分間保持して焼結した。さらに、950℃まで降温し、
30分間保持した後、 N、ガスで焼入れをした6その
後、これを550℃X100分間保持して焼戻しを行い
、ロックウェルC硬度58の焼結合金部材が得られた。
<Example 2> 83% by weight of alloy powder with the same composition and friction resistance as Example 1
After adding 2% by weight of acetone diluted with acetone to a mixed powder of 17% by weight of TaC powder with a particle size of 1.5μ and kneading, chips of the green compact were formed with a press pressure of 6.0 ton/-. Molded. Next, this compacted powder chip was pre-sintered in a hydrogen atmosphere at 600°C, and then placed in a 1120'c vacuum furnace for 20 minutes.
It was held for a minute to sinter. Furthermore, the temperature dropped to 950℃,
After holding for 30 minutes, it was quenched with N gas.Then, this was held at 550° C. for 100 minutes to temper, and a sintered alloy member with a Rockwell C hardness of 58 was obtained.

この焼結合金部材を実施例1と同じ方法にてロッカアー
ム化し、機械加工を行い1表面粗さRmax 1.6〜
2.5μのAQロッカアームを得た。
This sintered alloy member was made into a rocker arm using the same method as in Example 1, and machined to a surface roughness Rmax of 1.6 to
A 2.5μ AQ rocker arm was obtained.

第7図は焼結合金部材の組織を示す写真(400倍)で
ある。実施例1と同様に、マトリックスはソルバイト組
織である。白色部はCrの炭化物またはCr−Moの複
合炭化物からなる。マトリックスと白色部の境界に位置
する綿状白色81)は、TaCからなる。写真の通り、
TaCは微細で、かつ分散性が良好である。
FIG. 7 is a photograph (400x magnification) showing the structure of the sintered alloy member. As in Example 1, the matrix is a sorbite structure. The white part is made of Cr carbide or Cr-Mo composite carbide. The flocculent white 81) located at the boundary between the matrix and the white part consists of TaC. As the photo shows,
TaC is fine and has good dispersibility.

(発明の効果) 以上のように、本発明の焼結合金部材によれば次のよう
な効果が得られる。
(Effects of the Invention) As described above, the sintered alloy member of the present invention provides the following effects.

(1)微細な高硬度の炭化物が均一に分散しているので
、耐摩耗性において優れている。
(1) Excellent wear resistance because fine, highly hard carbides are uniformly dispersed.

(2)組織がソルバイト組織であるので、硬さおよび靭
性においても優れている。
(2) Since the structure is a sorbite structure, it has excellent hardness and toughness.

(3)パフ研摩または化学エツチングにより、微細なオ
イル保持凹部が分散性良く形成されるので。
(3) Puff polishing or chemical etching creates fine oil-holding recesses with good dispersion.

該凹部を備えた摺動部材は、摺動特性において優れてい
る。
A sliding member provided with the recessed portion has excellent sliding properties.

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

第1図はロッカアームの部分断面図、第2図は従来例の
焼結合金部材の組織を示す写真(倍率400)、第3図
は比較例の焼結合金部材の組織を示す写真(倍率400
)、第4図は実施例1の焼結合金部材の組織を示す写真
((8率400)、第5図は従来例の焼結合金部Hのパ
フ研摩後の摺動面を示す走査型電子顕微鏡による写真(
倍率1000)、第6図は実施例1の焼結合金部材のパ
フ研摩後の摺動面を示す走査型電子顕微鏡による写真(
倍率1000)、第7図は実施例2の焼結合金部材の組
織を示す写真(倍率400)である。 3・・・・焼結合金部材。 属 1 図 弔5署:     第6囮 第2才゛     第3互′j
Fig. 1 is a partial sectional view of the rocker arm, Fig. 2 is a photograph showing the structure of a conventional sintered alloy member (400 magnification), and Fig. 3 is a photo showing the structure of a comparative sintered alloy member (400 magnification).
), FIG. 4 is a photograph ((8 ratio: 400)) showing the structure of the sintered alloy member of Example 1, and FIG. 5 is a scanning type photograph showing the sliding surface of the sintered alloy part H of the conventional example after puff polishing. Photo taken with an electron microscope (
Fig. 6 is a photograph taken by a scanning electron microscope showing the sliding surface of the sintered alloy member of Example 1 after puff polishing (magnification: 1000).
FIG. 7 is a photograph (magnification: 400) showing the structure of the sintered alloy member of Example 2. 3...Sintered alloy member. Genus 1 Figure 5 stations: 6th decoy 2nd year 3rd year

Claims (1)

【特許請求の範囲】[Claims] (1)重量比でC:1.0〜4.0%、Cr:4.0〜
7.0%、およびP:0.5〜2.0%、Mo:2.0
〜6.0%、B:0.5〜3.0%のうちの少なくとも
一種を含有し、残部がFeおよび不可避成分からなる焼
結合金マトリックスに、平均粒径が10μ以下であるC
r_3C_2、NbC、TaC、TiC、WC、VC、
ZrC、HfCのうち少なくとも一種の炭化物を分散し
たソルバイト組織を有することを特徴とする耐摩耗性に
優れた焼結合金部材。
(1) C: 1.0-4.0%, Cr: 4.0-4.0% by weight
7.0%, P: 0.5-2.0%, Mo: 2.0
~6.0%, B: at least one of 0.5 to 3.0%, and the balance is Fe and unavoidable components.
r_3C_2, NbC, TaC, TiC, WC, VC,
A sintered alloy member having excellent wear resistance, characterized by having a sorbite structure in which at least one type of carbide among ZrC and HfC is dispersed.
JP1995286A 1986-01-30 1986-01-30 Sintered alloy member having excellent wear resistance Pending JPS62177159A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1995286A JPS62177159A (en) 1986-01-30 1986-01-30 Sintered alloy member having excellent wear resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1995286A JPS62177159A (en) 1986-01-30 1986-01-30 Sintered alloy member having excellent wear resistance

Publications (1)

Publication Number Publication Date
JPS62177159A true JPS62177159A (en) 1987-08-04

Family

ID=12013535

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1995286A Pending JPS62177159A (en) 1986-01-30 1986-01-30 Sintered alloy member having excellent wear resistance

Country Status (1)

Country Link
JP (1) JPS62177159A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6040357A (en) * 1998-05-28 2000-03-21 Dsm N.V. Method of making a radiation-curable ink composition, radiation-curable ink composition and ribbon assembly
US6085010A (en) * 1997-06-11 2000-07-04 Dsm N.V. Optical glass fiber ribbon assemblies and radiation-curable compositions for use in forming ribbon assemblies
US6130980A (en) * 1997-05-06 2000-10-10 Dsm N.V. Ribbon assemblies and ink coating compositions for use in forming the ribbon assemblies
US6301415B1 (en) 1997-08-14 2001-10-09 Dsm N.V Optical glass fiber ribbon assemblies, matrix forming compositions radiation-curable compositions
CN103537674A (en) * 2013-10-11 2014-01-29 芜湖市鸿坤汽车零部件有限公司 Powder metallurgy spring steel material and manufacturing method thereof
WO2020031702A1 (en) * 2018-08-07 2020-02-13 国立大学法人広島大学 Fe-based sintered body, fe-based sintered body production method, and hot-pressing die

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5985847A (en) * 1982-11-08 1984-05-17 Mitsubishi Metal Corp Fe-base sintered material for sliding member of internal-combustion engine
JPS6033181A (en) * 1983-07-30 1985-02-20 株式会社昭和製作所 Oil locking device for front fork

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5985847A (en) * 1982-11-08 1984-05-17 Mitsubishi Metal Corp Fe-base sintered material for sliding member of internal-combustion engine
JPS6033181A (en) * 1983-07-30 1985-02-20 株式会社昭和製作所 Oil locking device for front fork

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6130980A (en) * 1997-05-06 2000-10-10 Dsm N.V. Ribbon assemblies and ink coating compositions for use in forming the ribbon assemblies
US6085010A (en) * 1997-06-11 2000-07-04 Dsm N.V. Optical glass fiber ribbon assemblies and radiation-curable compositions for use in forming ribbon assemblies
US6301415B1 (en) 1997-08-14 2001-10-09 Dsm N.V Optical glass fiber ribbon assemblies, matrix forming compositions radiation-curable compositions
US6040357A (en) * 1998-05-28 2000-03-21 Dsm N.V. Method of making a radiation-curable ink composition, radiation-curable ink composition and ribbon assembly
CN103537674A (en) * 2013-10-11 2014-01-29 芜湖市鸿坤汽车零部件有限公司 Powder metallurgy spring steel material and manufacturing method thereof
WO2020031702A1 (en) * 2018-08-07 2020-02-13 国立大学法人広島大学 Fe-based sintered body, fe-based sintered body production method, and hot-pressing die
JP2020023733A (en) * 2018-08-07 2020-02-13 国立大学法人広島大学 Fe-BASED SINTERED BODY, METHOD FOR PRODUCING Fe-BASED SINTERED BODY, AND HOT PRESS DIE
US11858045B2 (en) 2018-08-07 2024-01-02 Hiroshima University Fe-based sintered body, Fe-based sintered body production method, and hot-pressing die

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