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JPH0559982B2 - - Google Patents
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JPH0559982B2 - - Google Patents

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Publication number
JPH0559982B2
JPH0559982B2 JP4563186A JP4563186A JPH0559982B2 JP H0559982 B2 JPH0559982 B2 JP H0559982B2 JP 4563186 A JP4563186 A JP 4563186A JP 4563186 A JP4563186 A JP 4563186A JP H0559982 B2 JPH0559982 B2 JP H0559982B2
Authority
JP
Japan
Prior art keywords
iron
alloy
carbon
valve seat
sintered alloy
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 - Fee Related
Application number
JP4563186A
Other languages
Japanese (ja)
Other versions
JPS6296662A (en
Inventor
Yukio Kadota
Akira Manabe
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.)
Toyota Motor Corp
Original Assignee
Toyota 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 Toyota Motor Corp filed Critical Toyota Motor Corp
Publication of JPS6296662A publication Critical patent/JPS6296662A/en
Publication of JPH0559982B2 publication Critical patent/JPH0559982B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 本発明は内燃期間のバルブシート用焼結合金に
係わり、より詳しくは合金自身の耐摩耗性を高め
るとともに、相手バルブに対する攻撃性を弱めた
鉄系焼結合金に関する。 〔従来の技術〕 最近、自動車用内燃機関は高出力、高回転化、
低燃費化が計られ、また排気ガス対策が施される
傾向にある。このため、バルブやバルブシート部
品は従来以上に厳しい条件にさらされるようにな
つている。 このバルブシートには高温での耐摩耗性を高め
るため、Cr、Ni、Co、Mo等の合金元素を添加
した鉄系焼結合金が多用されつつある。 〔発明が解決しようとする問題点〕 ところで、バルブシートは、自身の耐摩耗性を
向上させるとともに相手バルブへの攻撃性の低減
が求められており、バルブシートの材質の選択
は、相手バルブとの相関において決定されるべき
もので、この選択を誤るとバルブ自身の耐摩耗性
を弱めるばかりか、相手部材に対する攻撃性を増
して、バルブ機構全体に思わしくない影響を与え
ることになる。そのため、従来のような、例えば
ただ単にフエロモリブデン等の金属間化合物や複
合炭化物を添加して極度に耐摩耗性を高めたバル
ブシートをそのまま使用すると、エンジンバルブ
の摩耗を増大させる結果となる。 本発明は通常の耐摩耗性が特に高められていな
い汎用エンジンバルブ(例えばJIS NFC 751製)
を相手にした場合にも相手材を摩耗することな
く、又は自身の摩耗を著しく増大させることのな
いようにしようとするものである。 〔問題点を解決するための手段〕 本発明のバルブシート用鉄系焼結合金は、重量
比で、クロム(Cr)10〜70%、タングステン
(W)5〜20%、モリブデン(Mo)5〜20%、
炭素(C)0.5〜3%、鉄(Fe)20%以下及び残
部コバルト(Co)からなる合金粒子5〜25%を
炭素(C)0.5〜2%、所望によりニツケル(Ni)
1〜10%及び残部鉄(Fe)と不可避不純物から
なるパーライトを主体とする基地中に均一に分散
させたことを特徴とする。 また、本発明は前記焼結合金に鉛(Pb)1〜
20%を溶浸したことを特徴とする。 なお、本発明において%は特記しない限り重量
%を示す。 本発明で用いる各成分元素の限定理由について
説明する。 まず、硬質粒子として加える合金粒子の各成分
元素について説明する。 合金粒子中のCr(クロム)はC(炭素)と化合
して炭化物を形成するとともに一部がCoと合金
を形成し合金粒子の硬さを向上させる効果を有し
ているが、Crが10%未満では上記の効果が不十
分であり、70%を超えるとCrの拡散が周囲の基
地へ進み過ぎ、合金粒子の内部及び周縁に空隙を
生じ、合金粒子がもろくなる。そのためCrは10
〜70%と限定した。しかしながら、40〜70%がさ
らに好ましい。 W(タングステン)は、Cと化合してMC型の
硬質炭化物とCoとの複炭化物を形成し、合金粒
子の硬さを向上させるが、Wが5%未満ではその
効果が発揮されず、20%を超えると合金粒子が硬
くなり過ぎ、相手材であるバルブへの攻撃性が増
大するため、Wは5〜20%とした。 Mo(モリブデン)はCと化合して硬質炭化物
を形成し、合金粒子の硬さを増すが、Moが5%
未満ではその効果が現れず、20%を超えると合金
粒子が硬くなり過ぎて相手部材を攻撃するので5
〜20%とした。 CはCr、Mo及びWと化合して炭化物を形成
し、合金粒子の硬さを向上させるが、Cが0.5%
未満ではその効果が発揮されず、3%を超えると
炭化物量が多すぎてもろくなる。そのため、Cは
0.5〜3%とした。 Co(コバルト)は合金粒子において他の金属成
分の残部をなしており、粒子の耐熱性を向上させ
ると共に、一部が基地に拡散して粒子と基地の接
合性を向上させ、粒子の脱落を防止する効果があ
る。この効果は5%未満では得られにくく、ま
た、30%を超えてもその効果に変化がないため、
5〜30%とするのが好ましい。 Fe(鉄)は特に添加しなくてもよいが、バルブ
シートに必要とする強度等に問題がなければ、高
価なCoの代わりに20%以下の任意の範囲で用い
ることができる。また、Cr、W、Moを単体とし
てではなくフエロアロイとして合金の原料に用い
る場合に添加されることになる。 合金粒子は耐摩耗性の向上に効果があることか
ら用いられる。その粒径は20μm未満では耐摩耗
性が低下し、200μm以上では成形性、圧縮性が低
下し、耐摩耗性が低下する。そのため20〜200μm
とするのが好ましい。また、さらに好ましくは30
〜150μmである。合金粒子の硬さは、Hv1000未
満では粒子が摩耗しやすいため、耐摩耗性が発揮
されない。従つてHv1000以上とするのが好まし
い。合金粒子は、5%未満では得られる焼結合金
の耐摩耗効果が発揮されず、25%を超えると成形
性、圧縮性及び被削性が低下するとともに相手材
であるバルブへの攻撃性が増大するため、合金粒
子は5〜25%と限定した。 次に基地について説明する。 Cは基地のFeに固溶してパーライト組織を形
成し、焼結合金の強度と硬さを向上させ、また、
前記合金粒子中のCr、Mo及びWと化合して硬質
の炭化物を形成し、合金粒子の硬さを更に向上さ
せる効果があるとともに、未反応の遊離黒鉛が、
ある程度基地中に内在することにより、潤滑効果
が発揮されるが、Cが0.5%未満ではその効果が
なく、20%を超えるとセメンタイトが粗大化し遊
離黒鉛が多すぎて基地がもろくなるため、Cは
0.5〜2%とした。 Ni(ニツケル)はFe基地に固溶して基地の強度
を向上させるのに役立つため、更に強度を必要と
する場合に添加されるが、Niが1%未満ではそ
の効果が発揮されず、10%を超えると基地が軟化
し、耐摩耗性が低下するため、Niは1〜10%と
した。 Pb(鉛)の焼結合金への溶浸は、よりきびしい
条件下で使用されるバルブシートの場合に行われ
る。溶浸されたPbは、バルブとバルブシートの
接触部に介在してPb酸化物層を形成することに
より潤滑剤として作用してバルブ及びバルブシー
ト相互の耐摩耗性を向上させるが、Pbの溶浸が
1%未満ではPb溶浸の効果が発揮されず、20%
を超えて溶浸すると焼結合金のスケルトンが弱化
して摩耗が増大することから1〜20%とした。 〔実施例〕 本発明を実施例により説明する。以下の実施例
において%は重量%を表わす。 実施例 1 Cr30%、W10%、Mo10%、Fe10%、C25%及
び残部Coからなる合金アトマイズ粉(−100メツ
シユ)15%、黒鉛粉末(−350メツシユ)1.5%、
カルボニルNi粉末(10μm以下)4%及び残部還
元鉄粉(−100メツシユ)に潤滑剤としてステア
リン酸亜鉛粉末0.8%を混合した後、この混合粉
末を金型内に充てんし、成形圧7t/cm2で成形して
バルブシート粗形状の粉末成形体を得た。 この粉末成形体をアンモニア分解ガス雰囲気中
で1150℃の温度にて60分間焼結して焼結体を得
た。焼結体密度は7.0g/cm2。 得られた焼結体を排気弁座の形状に加工して排
気量2000c.c.4気筒のデイーゼルエンジンに装着
し、全負荷で200時間台上耐久試験を実施し、バ
ルブシート当り面幅増加量及びバルブ摩耗量を測
定した。なお、相手バルブにはJIS NFC 751を
用いた。 実施例 2〜4 各材料を第1表に示す各組成割合にそれぞれ配
合して実施例1と同様に行つて、各焼結体を得
た。なお、実施例3及び4は得られた焼結体を
Pb塊と接触させて再度アンモニア分解ガス雰囲
気中で1050℃の温度にて30分間加熱して焼結体中
にPbを溶浸したものである。 得られた各焼結体を弁座形状に加工し、バルブ
シート当り面幅増加量及びバルブ摩耗量を実施例
1と同様に試験したのち測定した。 実施例 5 Cr45%、W18%、Mo10%、Fe6%、C1%及び
残部Coからなる合金アトマイズ粉(−100メツシ
ユ)15%、黒鉛粉末(−350メツシユ)1.1%、カ
ルボニルNi粉末(10μm以下)2%及び残部還元
鉄粉(−100メツシユ)に潤滑剤としてステアリ
ン酸亜鉛粉末0.8%を混合した後、この混合粉末
を金型内に充てんし、成形圧7t/cm2で成形してバ
ルブシート粗形状の粉末成形体を得た。 この粉末成形体をアンモニア分解ガス雰囲気中
で1140℃の温度にて60分間焼結して焼結体を得
た。焼結体密度は7.0g/cm2。 得られた焼結体を排気弁座の形状に加工して排
気量2000c.c.4気筒のデイーゼルエンジンに装着
し、全負荷で300時間台上耐久試験を実施し、バ
ルブシート当り面幅増加量及びバルブ摩耗量を測
定した。なお、相手バルブにはJIS NFC 751を
用いた。 実施例 6〜8 各材料を第1表に示す各組成割合にそれぞれ配
合して実施例5と同様に行つて、各焼結体を得
た。なお、実施例7及び8は得られた焼結体を
Pb塊と接触させて再度アンモニア分解ガス雰囲
気中で1050℃の温度にて30分間加熱して焼結体中
にPbを溶浸したものである。 得られた各焼結体を弁座形状に加工し、バルブ
シート当り面幅増加量及びバルブ摩耗量を実施例
5と同様に試験したのち測定した。 なお、合金粒子の粒子径及び硬さを第2表に示
す。 比較例1及び2 比較例1としてJIS FC 30鋳鉄、比較例2とし
てJIS耐熱鋼材SUH4Bをそれぞれ用いて弁座形
状に加工し、これらを実施例1と同様に試験して
バルブシート当り面幅増加量及びバルブ摩耗量を
測定した。 以上の測定結果をまとめて第1表に示す。
[Industrial Field of Application] The present invention relates to a sintered alloy for valve seats during internal combustion, and more particularly to an iron-based sintered alloy that has improved wear resistance of the alloy itself and is less aggressive against mating valves. [Conventional technology] Recently, internal combustion engines for automobiles have been increasing in output and rotation speed.
There is a trend towards lower fuel consumption and measures against exhaust gas. For this reason, valves and valve seat components are now exposed to more severe conditions than ever before. In order to improve wear resistance at high temperatures, iron-based sintered alloys containing alloying elements such as Cr, Ni, Co, and Mo are increasingly being used for valve seats. [Problems to be solved by the invention] By the way, the valve seat is required to improve its own wear resistance and reduce its aggressiveness to the mating valve, and the selection of the material of the valve seat is dependent on the mating valve and the valve seat. If this selection is incorrect, it will not only weaken the wear resistance of the valve itself, but also increase its aggressiveness against the mating member, which will have an undesirable effect on the entire valve mechanism. Therefore, if conventional valve seats, for example, which have extremely high wear resistance by simply adding intermetallic compounds such as ferromolybdenum or composite carbides, are used as they are, engine valve wear will increase. . The present invention applies to general-purpose engine valves that do not have particularly high wear resistance (e.g., manufactured by JIS NFC 751).
The aim is to avoid abrasion of the mating material or a significant increase in wear of the mating material even when the mating material is used as a mating material. [Means for Solving the Problems] The iron-based sintered alloy for valve seats of the present invention contains, by weight, chromium (Cr) 10 to 70%, tungsten (W) 5 to 20%, and molybdenum (Mo) 5%. ~20%,
5 to 25% alloy particles consisting of 0.5 to 3% carbon (C), 20% or less iron (Fe), and the balance cobalt (Co), 0.5 to 2% carbon (C), and optionally nickel (Ni).
It is characterized by being uniformly dispersed in a matrix mainly composed of pearlite, which is composed of 1 to 10% iron (Fe) and inevitable impurities. Further, the present invention provides that the sintered alloy contains 1 to 10% of lead (Pb).
Characterized by 20% infiltration. In the present invention, % indicates weight % unless otherwise specified. The reason for limiting each component element used in the present invention will be explained. First, each component element of the alloy particles added as hard particles will be explained. Cr (chromium) in the alloy particles combines with C (carbon) to form carbides, and a portion also forms an alloy with Co, which has the effect of improving the hardness of the alloy particles. If it is less than 70%, the above effect is insufficient, and if it exceeds 70%, the diffusion of Cr will proceed too much to the surrounding base, creating voids inside and at the periphery of the alloy particles, making the alloy particles brittle. Therefore Cr is 10
Limited to ~70%. However, 40-70% is more preferred. W (tungsten) combines with C to form a double carbide of MC-type hard carbide and Co, improving the hardness of the alloy particles, but this effect is not exhibited when W is less than 5%. If the W content exceeds 5%, the alloy particles become too hard and attack against the valve, which is the mating material, increases, so W is set at 5 to 20%. Mo (molybdenum) combines with C to form hard carbides and increases the hardness of alloy particles, but Mo
If it is less than 20%, the effect will not appear, and if it exceeds 20%, the alloy particles will become too hard and attack the mating material.
~20%. C combines with Cr, Mo and W to form carbides and improves the hardness of alloy particles, but when C is 0.5%
If it is less than 3%, the effect will not be exhibited, and if it exceeds 3%, the amount of carbide will be too large and it will become brittle. Therefore, C is
It was set at 0.5 to 3%. Co (cobalt) forms the remainder of other metal components in the alloy particles, and it improves the heat resistance of the particles, and a portion of it diffuses into the matrix, improving the bonding properties between the particles and the matrix, and preventing the particles from falling off. It has the effect of preventing This effect is difficult to obtain when it is less than 5%, and there is no change in the effect even when it exceeds 30%.
It is preferably 5 to 30%. Fe (iron) does not need to be particularly added, but if there is no problem with the strength required for the valve seat, it can be used in any range of 20% or less in place of the expensive Co. Furthermore, when Cr, W, and Mo are used as raw materials for alloys as ferroalloys rather than as single substances, they are added. Alloy particles are used because they are effective in improving wear resistance. When the particle size is less than 20 μm, wear resistance decreases, and when it is 200 μm or more, moldability and compressibility decrease, resulting in a decrease in wear resistance. Therefore 20~200μm
It is preferable that Also, more preferably 30
~150 μm. If the hardness of the alloy particles is less than 1000 Hv, the particles will easily wear out, so wear resistance will not be exhibited. Therefore, it is preferable to set it to Hv1000 or more. If the alloy particles are less than 5%, the resulting sintered alloy will not exhibit the wear-resisting effect, and if it exceeds 25%, the formability, compressibility, and machinability will decrease, and the mating material, the valve, will be attacked. The alloy particles were limited to 5 to 25% due to the increase in the amount of alloy particles. Next, I will explain the base. C forms a solid solution in the base Fe to form a pearlite structure, improving the strength and hardness of the sintered alloy, and
It combines with Cr, Mo, and W in the alloy particles to form hard carbides, which has the effect of further improving the hardness of the alloy particles, and unreacted free graphite.
C has a lubricating effect by being present in the base to some extent, but if it is less than 0.5%, it has no effect, and if it exceeds 20%, the cementite becomes coarse and there is too much free graphite, making the base brittle. teeth
It was set at 0.5 to 2%. Ni (nickel) dissolves in the Fe base and helps improve the strength of the base, so it is added when further strength is required, but if Ni is less than 1%, its effect will not be exhibited, and 10 If the Ni content exceeds 1%, the base becomes soft and the wear resistance decreases, so the Ni content was set to 1 to 10%. Infiltration of sintered alloys with Pb (lead) is carried out in the case of valve seats used under more severe conditions. The infiltrated Pb acts as a lubricant by forming a Pb oxide layer at the contact area between the valve and the valve seat, improving mutual wear resistance between the valve and the valve seat. If the Pb infiltration is less than 1%, the effect of Pb infiltration will not be exhibited;
If infiltration exceeds 1%, the skeleton of the sintered alloy will weaken and wear will increase, so it was set at 1% to 20%. [Example] The present invention will be explained with reference to an example. In the following examples, percentages refer to percentages by weight. Example 1 Alloy atomized powder (-100 mesh) 15%, graphite powder (-350 mesh) 1.5%, consisting of 30% Cr, 10% W, 10% Mo, 10% Fe, 25% C, and the balance Co.
After mixing 0.8% zinc stearate powder as a lubricant with 4% carbonyl Ni powder (10μm or less) and the balance reduced iron powder (-100 mesh), this mixed powder was filled into a mold and the molding pressure was 7t/cm. 2 to obtain a powder compact with a rough valve seat shape. This powder compact was sintered at a temperature of 1150°C for 60 minutes in an ammonia decomposition gas atmosphere to obtain a sintered body. The density of the sintered body is 7.0g/cm 2 . The obtained sintered body was processed into the shape of an exhaust valve seat and installed in a 2000 c.c. 4-cylinder diesel engine, and a bench durability test was conducted for 200 hours under full load to increase the surface width of the valve seat. The amount of wear and valve wear were measured. Note that JIS NFC 751 was used for the mating valve. Examples 2 to 4 Each material was blended in the respective composition ratios shown in Table 1 and the same procedure as in Example 1 was carried out to obtain each sintered body. In addition, in Examples 3 and 4, the obtained sintered body was
The sintered body was brought into contact with the Pb lump and heated again at a temperature of 1050°C for 30 minutes in an ammonia decomposition gas atmosphere to infiltrate Pb into the sintered body. Each of the obtained sintered bodies was processed into a valve seat shape, and the increase in surface width per valve seat and the amount of valve wear were tested and measured in the same manner as in Example 1. Example 5 Alloy atomized powder consisting of 45% Cr, 18% W, 10% Mo, 6% Fe, 1% C, and the balance Co (-100 mesh) 15%, graphite powder (-350 mesh) 1.1%, carbonyl Ni powder (10 μm or less) After mixing 0.8% zinc stearate powder as a lubricant with 2% and the balance reduced iron powder (-100 mesh), this mixed powder is filled into a mold and molded at a molding pressure of 7t/cm 2 to form a valve seat. A roughly shaped powder compact was obtained. This powder compact was sintered at a temperature of 1140° C. for 60 minutes in an ammonia decomposition gas atmosphere to obtain a sintered body. The density of the sintered body is 7.0g/cm 2 . The obtained sintered body was processed into the shape of an exhaust valve seat and installed in a 2000 c.c. 4-cylinder diesel engine, and a bench durability test was conducted for 300 hours under full load, resulting in an increase in the surface width of the valve seat. The amount of wear and valve wear were measured. Note that JIS NFC 751 was used for the mating valve. Examples 6 to 8 Each material was blended in the respective composition ratios shown in Table 1 and the same procedure as in Example 5 was carried out to obtain each sintered body. In addition, in Examples 7 and 8, the obtained sintered body was
The sintered body was brought into contact with the Pb lump and heated again at a temperature of 1050°C for 30 minutes in an ammonia decomposition gas atmosphere to infiltrate Pb into the sintered body. Each of the obtained sintered bodies was processed into a valve seat shape, and the amount of increase in surface width per valve seat and the amount of valve wear were tested and measured in the same manner as in Example 5. In addition, the particle diameter and hardness of the alloy particles are shown in Table 2. Comparative Examples 1 and 2 JIS FC 30 cast iron as Comparative Example 1 and JIS heat-resistant steel SUH4B as Comparative Example 2 were processed into a valve seat shape, and tested in the same manner as Example 1 to increase the face width per valve seat. The amount of wear and valve wear were measured. The above measurement results are summarized in Table 1.

【表】【table】

〔発明の効果〕〔Effect of the invention〕

本発明のバルブシート用鉄系焼結合金は上記し
たように合金粒子をパーライトを主体とする鉄基
地中に均一に分散させたので耐摩耗性に優れ、か
つ相手材であるバルブに対する攻撃性が低く、バ
ルブシート用焼結合金として最適なものである。
As mentioned above, the iron-based sintered alloy for valve seats of the present invention has alloy particles uniformly dispersed in an iron base mainly composed of pearlite, so it has excellent wear resistance and is less aggressive against the mating material of the valve. It is a low alloy sintered alloy suitable for valve seats.

Claims (1)

【特許請求の範囲】 1 重量比で、クロム(Cr)10〜70%、タング
ステン(W)5〜20%、モリブデン(Mo)5〜
20%、炭素(C)0.5〜3%、鉄(Fe)20%以下
及び残部コバルト(Co)からなる合金粒子5〜
25%を炭素(C)0.5〜2%及び残部鉄(Fe)と
不可避不純物からなるパーライトを主体とする基
地中に均一に分散させたことを特徴とするバルブ
シート用鉄系焼結合金。 2 合金粒子の中のクロム(Cr)の含有量が重
量比で40〜70%であることを特徴とする特許請求
の範囲第1項記載のバルブシート用鉄系焼結合
金。 3 合金粒子の粒子径が20〜200μmであり、合金
粒子の硬さがHv1000以上であることを特徴とす
る特許請求の範囲第1項記載のバルブシート用鉄
系焼結合金。 4 重量比で、クロム(Cr)10〜70%、タング
ステン(W)5〜20%、モリブデン(Mo)5〜
20%、炭素(C)0.5〜3%、鉄(Fe)20%以下
及び残部コバルト(Co)からなる合金粒子5〜
25%を炭素(C)0.5〜2%、ニツケル(Ni)1
〜10%及び残部鉄(Fe)と不可避不純物からな
るパーライトを主体とする基地中に均一に分散さ
せたことを特徴とするバルブシート用鉄系焼結合
金。 5 合金粒子中のクロム(Cr)の含有量が重量
比で40〜70%であることを特徴とする特許請求の
範囲第4項記載のバルブシート用鉄系焼結合金。 6 合金粒子の粒子径が20〜200μmであり、合金
粒子の硬さがHv1000以上であることを特徴とす
る特許請求の範囲第4項記載のバルブシート用鉄
系焼結合金。 7 重量比で、クロム(Cr)10〜70%、タング
ステン(W)5〜20%、モルブデン(Mo)5〜
20%、炭素(C)0.5〜3%、鉄(Fe)20%以下
及び残部コバルト(Co)からなる合金粒子5〜
25%を炭素(C)0.5〜2%及び残部鉄(Fe)と
不可避不純物からなるパーライトを主体とする基
地中に均一に分散してなる焼結合金に鉛(Pb)
1〜20%を溶浸したことを特徴とするバルブシー
ト用鉄系焼結合金。 8 合金粒子中のクロム(Cr)の含有量が重量
比で40〜70%であることを特徴とする特許請求の
範囲第7項記載のバルブシート用鉄系焼結合金。 9 合金粒子の粒子径が20〜200μmであり、合金
粒子の硬さがHv1000以上であることを特徴とす
る特許請求の範囲第7項記載のバルブシート用鉄
系焼結合金。 10 重量比で、クロム(Cr)10〜70%、タン
グステン(W)5〜20%、モリブデン(Mo)5
〜20%、炭素(C)0.5〜3%、鉄(Fe)20%以
下及び残部コバルト(Co)からなる合金粒子5
〜25%を炭素(C)0.5〜2%、ニツケル(Ni)
1〜10%及び残部鉄(Fe)と不可避不純物から
なるパーライトを主体とする基地中に均一に分散
してなる焼結合金に鉛(Pb)1〜20%を溶浸し
たことを特徴とするバルブシート用鉄系焼結合
金。 11 合金粒子中のクロム(Cr)の含有量が重
量比で40〜70%であることを特徴とする特許請求
の範囲第10項記載のバルブシート用鉄系焼結合
金。 12 合金粒子の粒子径が20〜200μmであり、合
金粒子の硬さがHv1000以上であることを特徴と
する特許請求の範囲第10項記載のバルブシート
用鉄系焼結合金。
[Claims] 1. Chromium (Cr) 10 to 70%, tungsten (W) 5 to 20%, molybdenum (Mo) 5 to 70% by weight
20% carbon (C), 0.5 to 3% carbon (C), 20% or less iron (Fe), and the balance cobalt (Co) 5 to
An iron-based sintered alloy for valve seats, characterized in that 25% of carbon (C) is uniformly dispersed in a pearlite-based matrix consisting of 0.5 to 2% of carbon (C) and the balance iron (Fe) and inevitable impurities. 2. The iron-based sintered alloy for a valve seat according to claim 1, wherein the content of chromium (Cr) in the alloy particles is 40 to 70% by weight. 3. The iron-based sintered alloy for a valve seat according to claim 1, wherein the alloy particles have a particle diameter of 20 to 200 μm and a hardness of Hv1000 or more. 4 By weight, chromium (Cr) 10-70%, tungsten (W) 5-20%, molybdenum (Mo) 5-5%
20% carbon (C), 0.5 to 3% carbon (C), 20% or less iron (Fe), and the balance cobalt (Co) 5 to
25%, carbon (C) 0.5-2%, nickel (Ni) 1
An iron-based sintered alloy for valve seats, characterized by being uniformly dispersed in a pearlite-based matrix consisting of ~10% iron (Fe) and inevitable impurities. 5. The iron-based sintered alloy for a valve seat according to claim 4, wherein the content of chromium (Cr) in the alloy particles is 40 to 70% by weight. 6. The iron-based sintered alloy for a valve seat according to claim 4, wherein the alloy particles have a particle diameter of 20 to 200 μm and a hardness of Hv1000 or more. 7 By weight, chromium (Cr) 10-70%, tungsten (W) 5-20%, molybdenum (Mo) 5-5%
20% carbon (C), 0.5 to 3% carbon (C), 20% or less iron (Fe), and the balance cobalt (Co) 5 to
Lead (Pb) is added to a sintered alloy in which 25% of lead (Pb) is uniformly dispersed in a pearlite-based matrix consisting of 0.5-2% carbon (C) and the balance iron (Fe) and inevitable impurities.
An iron-based sintered alloy for valve seats characterized by infiltration of 1 to 20%. 8. The iron-based sintered alloy for a valve seat according to claim 7, wherein the content of chromium (Cr) in the alloy particles is 40 to 70% by weight. 9. The iron-based sintered alloy for a valve seat according to claim 7, wherein the alloy particles have a particle diameter of 20 to 200 μm and a hardness of Hv1000 or more. 10 Weight ratio: chromium (Cr) 10-70%, tungsten (W) 5-20%, molybdenum (Mo) 5
Alloy particles 5 consisting of ~20%, carbon (C) 0.5 to 3%, iron (Fe) 20% or less, and the balance cobalt (Co)
~25% carbon (C) 0.5~2%, nickel (Ni)
It is characterized by infiltrating 1-20% of lead (Pb) into a sintered alloy that is uniformly dispersed in a pearlite-based base consisting of 1-10% lead (Pb) and the balance iron (Fe) and unavoidable impurities. Iron-based sintered alloy for valve seats. 11. The iron-based sintered alloy for a valve seat according to claim 10, wherein the content of chromium (Cr) in the alloy particles is 40 to 70% by weight. 12. The iron-based sintered alloy for a valve seat according to claim 10, wherein the alloy particles have a particle diameter of 20 to 200 μm and a hardness of Hv1000 or more.
JP4563186A 1985-06-10 1986-03-03 Sintered iron alloy for valve seat Granted JPS6296662A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP12593385 1985-06-10
JP60-125933 1985-06-10

Publications (2)

Publication Number Publication Date
JPS6296662A JPS6296662A (en) 1987-05-06
JPH0559982B2 true JPH0559982B2 (en) 1993-09-01

Family

ID=14922552

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4563186A Granted JPS6296662A (en) 1985-06-10 1986-03-03 Sintered iron alloy for valve seat

Country Status (1)

Country Link
JP (1) JPS6296662A (en)

Also Published As

Publication number Publication date
JPS6296662A (en) 1987-05-06

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