JPS6140001B2 - - Google Patents
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- Publication number
- JPS6140001B2 JPS6140001B2 JP11438280A JP11438280A JPS6140001B2 JP S6140001 B2 JPS6140001 B2 JP S6140001B2 JP 11438280 A JP11438280 A JP 11438280A JP 11438280 A JP11438280 A JP 11438280A JP S6140001 B2 JPS6140001 B2 JP S6140001B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- valve
- valve seat
- sintered body
- 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.)
- Expired
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- Powder Metallurgy (AREA)
Description
この発明は、すぐれた耐摩耗性を有し、かつ組
織的にきわめて安定なFe基焼結合金製弁座の製
造法に関するものである。
従来、一般にFe基焼結合金製弁座は、C:0.5
〜1.5%、Cr:1〜10%を含有し、さらに必要に
応じてNiおよびCoのいずれか、または両方:1
〜15%、および/またはMoおよびWのいずれ
か、または両方:1〜15%を含有し、残りがFe
と不可避不純物からなる組成(以上重量%、以下
%はすべて重量%を意味する)を有する焼結体
を、焼結後急冷することによつて製造されてい
た。
しかし、上記従来Fe基焼結合金製弁座におい
ては、その組織が、通常マルテンサイトと残留オ
ーステナイトの混合組織からなるため、例えばこ
れをエンジンの鋳鉄製ヘツドに焼ばめにより取付
けて使用した場合、前記焼ばめ時あるいは使用時
の温度上昇により前記残留オーステナイトがマル
テンサイト変態を起し、このマルテンサイト変態
により弁座は寸法変化(膨張)を起すことから、
前記弁座がエンジンヘツドより脱落することがし
ばしば発生し、さらに前記残留オーステナイトの
存在によつて所望の耐摩耗性確保も困難であつ
た。
そこで、このような不安定な組織、すなわち残
留オーステナイトの存在する組織を有する従来
Fe基焼結合金製弁座に焼戻し処理を施して組織
の安定化をはかる試みもなされたが、この焼戻し
処理によつても残留オーステナイトを皆無とする
ことができないばかりか、むしろマルテンサイト
がソルバイト化するために硬さ低下をきたし、耐
摩耗性の低下をもたらすものであつた。
本発明者等は、上述のような観点から、従来
Fe基焼結合金製弁座のもつ問題点を解決すべく
研究を行なつた結果、上記の従来Fe基焼結合金
製弁座にCuを合金成分として原料粉末に配合す
るか、あるいは焼結後にCu含浸処理により含有
させるかして、CのFe基地中への固溶量を増大
させ、ついで、前記Cu含有によつて焼入れ処理
後、残留オーステナイトを多く含むようになつた
前記弁座にサブゼロ処理を施して前記残留オース
テナイトをマルテンサイト変態させると共に、C
を多く固溶したマルテンサイト組織とし、引続い
て焼戻し処理を施して固溶Cを炭化物として析出
させると、硬さがきわめて高く、かつ熱影響を全
く受けない安定した組織のFe基焼結合金製弁座
が得られるという知見を得たのである。
この発明は、上記知見にもとづいてなされたも
のであつて、C:0.5〜1.5%、Cr:1〜10%、
Cu:1〜30%を含有し、さらに必要に応じてNi
およびCoのうちの1種または2種:1〜15%、
および/またはMoおよびWのうちの1種または
2種:1〜15%を含有し、残りがFeと不可避不
純物からなる組成を有する焼結体、またはCo含
浸焼結体を、900〜1200℃の温度から焼入れし、−
20℃以下の温度でサブゼロ処理し、引続いて400
〜700℃の温度で焼戻し処理することからなるFe
基焼結合金製弁座の製造法に特徴を有するもので
ある。
つぎに、この発明のFe基焼結合金製弁座にお
いて、成分、組成範囲、焼入れ温度、サブゼロ処
理温度、および焼戻し温度を上記の通りに限定し
た理由を説明する。
(a) 成分組成
C
C成分には、素地に固溶してこれを強化すると
共に、炭化物を形成して耐摩耗性を向上させる作
用があるが、その含有量が0.5%未満では前記作
用に所望の効果が得られず、一方1.5%を越えて
含有させると、脆化が著しくなるほか、硬さ上昇
も著しくなり、相手材たる弁への攻撃性が増すよ
うになることから、その含有量を0.5〜1.5%と定
めた。
Cr
Cr成分には、大部分のCと結合して炭化物を
形成し、耐摩耗性を向上させるほか、素地に固溶
して耐熱性を向上させる作用があるが、その含有
量が1%未満では前記作用に所望の向上効果が得
られず、一方10%を越えて含有させると、強度が
急激に低下するようになると共に、硬さの上昇に
よつて弁の損傷が著しく増大するようになること
から、その含有量を1〜10%と定めた。
Cu
上記のようにCu成分には、素地中へのCの固
溶量を増大させ、これによつてサブゼロ処理によ
る残留オーステナイトを含まない微細マルテンサ
イト組織の確保、並びに焼戻し処理による炭化物
の析出を可能ならしめる作用があるほか、多量に
含有した場合には熱伝導性が向上して弁の冷却効
率を増大させる作用があるが、その含有量が1%
未満では前記作用に所望の効果が得られず、一方
30%を越えて含有させると、強度低下が著しくな
ることから、その含有量を1〜30%と定めた。
NiおよびCo
これらの成分には、素地に固溶して、これを強
化し、かつ耐熱性を向上させる均等的作用がある
ので、特に高い強度および耐熱性が要求される場
合に必要に応じて添加含有されるが、その含有量
が1%未満では前記作用に所望の改善効果が得ら
れず、一方15%を越えて含有させても、さらに一
段の改善効果は現われず、経済性を考慮して、そ
の含有量を1〜15%と定めた。
MoおよびW
これらの成分には、Crと同様にCと結合して
炭化物を形成するほか、未拡散のフエロモリブデ
ン粒子およびフエロタングステン粒子として素地
中に分散して耐摩耗性を向上させ、さらに素地に
固溶してその耐熱性を向上させる均等的作用があ
らるので、特に耐摩耗性および耐熱性が要求され
る場合に必要に応じて含有されるが、その含有量
が1%未満では前記作用に所望の向上効果が得ら
れず、一方15%を越えて含有させると、脆化が著
しく、強度が劣化するようになるばかりでなく、
被削性も著しくそこなわれるようになることか
ら、その含有量を1〜15%と定めた。
(b) 焼入れ温度
900℃未満の焼入れ温度では、焼戻し処理後、
所望の高硬度を確保することができず、一方1200
℃を越えた焼入れ温度は、1200℃が焼結温度の上
限値であることから、組織の著しい粗大化をもた
らすようになるので、焼入れ温度を900〜1200℃
と定めた。
(c) サブゼロ処理温度
−20℃を越えて高い温度では、残留オーステナ
イトが多く存在した組織しか得られず、しかもマ
ルテンサイトも微細化しないので、その上限値を
−20℃とすることによつて、残留オーステナイト
の存在しない微細なマルテンサイト組織の確保を
はかつた。
(d) 焼戻し温度
エンジンヘツドへの弁座の焼ばめ取付け、およ
び弁座の使用に際しては、前記弁座は300℃以上
の温度に加熱されるようになるので、400℃以上
の温度で焼戻し処理を施すことによつて組織の安
定化と炭化物析出による硬さ上昇をはかる必要が
ある。しかし700℃を越えた温度での焼戻し処理
は、硬さの著しい低下をもたらすことから、その
上限温度を700℃としなければならない。
つぎに、この発明の方法を実施例により比較例
と対比しながら説明する。
実施例 1
原料粉末として、粒度:−100meshのFe粉
末、同−100meshのFe−Cr合金(Cr:12%含
有)粉末、同−100mecshのCu粉末、同−
100meshの炭素粉末、同−200meshのNi粉末、同
−200meshのCo粉末、同−200meshのFe−Mo金
(Mo:60%含有)粉末、および同−200meshのFe
−W合金(W:75%含有)粉末を用意し、これら
原料粉末を第1表に示される配合組成に配合し、
混合し、6ton/cm2の圧力で圧粉体に成形し、つい
で水素雰囲気中、温度:1170℃に1時間保持して
焼結した後、この焼結温度より急冷による焼入れ
を行ない、引続いて液体窒素を用い、温度:−
150℃に15分間保持のサブゼロ処理を行ない、最
終的にアンモニア分解ガス中、温度:550℃に1
時間保持の焼戻し処理を施すことによつて配合組
成と実質的に同一の組成をもつた本発明弁座1〜
22をそれぞれ製造した。
The present invention relates to a method for manufacturing a valve seat made of an Fe-based sintered alloy that has excellent wear resistance and is structurally extremely stable. Conventionally, valve seats made of Fe-based sintered alloy generally have a C: 0.5.
~1.5%, Cr: 1 to 10%, and optionally either Ni or Co, or both: 1
~15% and/or Mo and/or W: 1~15%, the remainder being Fe.
It was manufactured by rapidly cooling a sintered body having a composition (all percentages by weight, all percentages by weight) consisting of and unavoidable impurities. However, since the conventional valve seat made of Fe-based sintered alloy mentioned above usually has a mixed structure of martensite and retained austenite, for example, when it is used by being attached to the cast iron head of an engine by shrink fit, , the retained austenite undergoes martensitic transformation due to the temperature increase during shrink fitting or use, and this martensitic transformation causes the valve seat to undergo dimensional changes (expansion).
The valve seat often falls off from the engine head, and furthermore, the presence of the retained austenite makes it difficult to maintain desired wear resistance. Therefore, conventional methods with such an unstable structure, that is, a structure in which retained austenite exists,
Attempts have been made to stabilize the structure by subjecting the valve seat made of Fe-based sintered alloy to a tempering process, but even with this tempering process, it is not possible to completely eliminate residual austenite. This resulted in a decrease in hardness and a decrease in wear resistance. From the above-mentioned viewpoint, the present inventors have proposed
As a result of research to solve the problems of valve seats made of Fe-based sintered alloy, we have found that Cu can be added to the raw material powder as an alloying component to the conventional valve seats made of Fe-based sintered alloy, or sintered Later, Cu is added through impregnating treatment to increase the solid solution amount of C in the Fe base, and then, due to the Cu inclusion, after quenching, the valve seat contains a large amount of retained austenite. Sub-zero treatment is performed to transform the retained austenite to martensite, and C
By creating a martensitic structure with a large amount of solid solution of C, and then subjecting it to a tempering treatment to precipitate the solid solution C as carbide, an Fe-based sintered alloy with extremely high hardness and a stable structure that is completely unaffected by heat can be created. This led to the discovery that a valve seat could be produced. This invention was made based on the above findings, and includes C: 0.5 to 1.5%, Cr: 1 to 10%,
Contains Cu: 1 to 30%, and further Ni as necessary.
and one or two of Co: 1 to 15%,
and/or one or two of Mo and W: 1 to 15%, and the remainder is Fe and inevitable impurities, or a Co-impregnated sintered body is heated to 900 to 1200°C. Quenched from a temperature of -
Subzero treatment at temperatures below 20°C followed by 400°C
Fe consisting of tempering treatment at a temperature of ~700℃
This method is unique in the manufacturing method of a valve seat made of sintered alloy. Next, in the Fe-based sintered alloy valve seat of the present invention, the reason why the components, composition range, quenching temperature, sub-zero treatment temperature, and tempering temperature are limited as described above will be explained. (a) Component composition C The C component has the effect of forming a solid solution in the base material and strengthening it, as well as forming carbide and improving wear resistance, but if its content is less than 0.5%, the above effect will not be achieved. If the desired effect is not obtained, and on the other hand, if the content exceeds 1.5%, embrittlement will become significant, hardness will also increase significantly, and the aggressiveness of the valve, which is the mating material, will increase. The amount was determined to be 0.5-1.5%. Cr The Cr component combines with most of the C to form carbides and improves wear resistance, as well as solid solution in the base material and improves heat resistance, but if the content is less than 1% However, if the content exceeds 10%, the strength will rapidly decrease and the damage to the valve will increase significantly due to the increase in hardness. Therefore, the content was set at 1 to 10%. Cu As mentioned above, the Cu component increases the solid solution amount of C in the matrix, thereby ensuring a fine martensitic structure that does not contain residual austenite through sub-zero treatment, and preventing the precipitation of carbides through tempering treatment. In addition, when it is contained in a large amount, it has the effect of improving thermal conductivity and increasing the cooling efficiency of the valve, but the content is 1%.
If it is less than the desired effect, the desired effect cannot be obtained;
If the content exceeds 30%, the strength decreases significantly, so the content was set at 1 to 30%. Ni and Co These components have the uniform effect of solid-dissolving in the base material, strengthening it, and improving heat resistance, so they can be used as needed when particularly high strength and heat resistance are required. However, if the content is less than 1%, the desired improvement effect on the above action cannot be obtained, and on the other hand, even if the content exceeds 15%, no further improvement effect will be obtained, and economic efficiency should be considered. The content was determined to be 1-15%. Mo and W These components, like Cr, combine with C to form carbides, and also disperse in the base material as undiffused ferromolybdenum particles and ferrotungsten particles to improve wear resistance. In addition, it is dissolved in the base material and has a uniform effect of improving its heat resistance, so it is included as necessary when particularly abrasion resistance and heat resistance are required, but the content is less than 1%. However, if the content exceeds 15%, not only will embrittlement become significant and the strength will deteriorate.
The content was set at 1 to 15% since machinability would be significantly impaired. (b) Quenching temperature At a quenching temperature of less than 900℃, after tempering treatment,
While unable to ensure the desired high hardness, 1200
Since 1200°C is the upper limit of sintering temperature, a quenching temperature exceeding 1200°C will result in significant coarsening of the structure.
It was determined that (c) Sub-zero treatment temperature If the temperature is higher than -20℃, only a structure with a large amount of retained austenite will be obtained, and martensite will not be refined, so by setting the upper limit to -20℃, , we ensured a fine martensitic structure with no retained austenite. (d) Tempering temperature When attaching the valve seat to the engine head by shrink-fitting and using the valve seat, the valve seat will be heated to a temperature of 300°C or higher, so it must be tempered at a temperature of 400°C or higher. It is necessary to stabilize the structure and increase hardness through carbide precipitation through treatment. However, tempering treatment at a temperature exceeding 700°C causes a significant decrease in hardness, so the upper limit temperature must be set at 700°C. Next, the method of the present invention will be explained using examples and comparing with comparative examples. Example 1 As raw material powders, Fe powder with a particle size of -100mesh, Fe-Cr alloy (containing Cr: 12%) powder with a particle size of -100mesh, Cu powder with a particle size of -100mesh, and -
100mesh carbon powder, -200mesh Ni powder, -200mesh Co powder, -200mesh Fe-Mo gold (Mo: 60% content) powder, and -200mesh Fe
- Prepare W alloy (W: 75% content) powder, blend these raw material powders into the composition shown in Table 1,
The mixture was mixed and formed into a green compact under a pressure of 6 tons/cm 2 , and then sintered in a hydrogen atmosphere at a temperature of 1170°C for 1 hour. using liquid nitrogen, temperature: -
Sub-zero treatment is carried out by holding at 150℃ for 15 minutes, and finally at 550℃ in ammonia decomposition gas.
Valve seats 1 to 1 of the present invention having substantially the same composition as the blended composition by subjecting to time-maintenance tempering treatment.
22 were produced respectively.
【表】【table】
【表】
また比較の目的で、第1表に示されるように構
成成分のうちのいずれかが、この発明の範囲から
外れた組成をもつ以外は、上記本発明弁座の製造
条件と同一の条件にて比較弁座1〜6をそれぞれ
製造した。
さらに、第1表に示されるように焼入れ温度、
サブゼロ処理温度および焼戻し処理温度のいずれ
かが、この発明の範囲から外れる以外は、上記本
発明弁座2の製造条件と同一の条件にて比較弁座
7〜11をそれぞれ製造した。
なお、第1表には、これらの比較弁座1〜11に
関し、この発明の範囲から外れた条件に※印を付
した。
ついで、この結果得られた本発明弁座1〜22お
よび比較弁座1〜11について、ロツクウエル硬さ
を測定すると共に、弁材:オーステナイト鋼、弁
温度:900℃、弁リフト量:6.8mm、弁座温度:
350℃、着座荷重:40Kg、回転数:3000r.p.m
(雰囲気:LPG燃焼ガス、試験時間:50時間の条
件で耐摩耗性試験を行ない、弁および弁座の摩耗
性を装定した。これらの測定結果を第1表に合せ
て示した。
さらに、上記本発明弁座1〜22および比較弁座
1〜11を、ヘツド材:FC20(鋳鉄)および
AC5A(A合金)、圧入面ヘツド寸法:44.00±
0.01mm、圧入面弁座寸法:44.1±0.01mm、圧入
代:100μm、ヘツド寸法:44mmφ×90mmφ×2.0
mm、弁座寸法:44.1mmφ×34mmφ×8mm、圧入荷
重:800〜1000Kg(鋳鉄ヘツドの場合)および
1000〜1300Kg(A合金ヘツドの場合)の条件
で、鋳鉄ヘツドおよびA合金ヘツドに嵌合取付
け、この状態で大気中、温度:500℃に10時間加
熱保持した後、前記ヘツドよりの前記弁座の抜出
荷重をそれぞれ測定した。この測定結果も合せて
示した。
第1表に示される結果から明らかなように、い
ずれかの条件がこの発明の範囲から外れた普較弁
座1〜11においては、耐摩耗性、相手攻撃性、お
よび抜出荷重の少なくともいずれかが劣つたもの
になつているのに対して、本発明弁座1〜22にお
いては、いずれもすぐれた耐摩耗性を有し、しか
も相手攻撃性も小さく、かつ抜出荷重もきわめて
大きなものになつている。
実施例 2
原料粉末として、粒度:−100meshのFe粉
末、同−100meshのFe−Cr合金(Cr:12%含
有)粉末、同−100meshの炭素粉末、同−
100meshのCu粉末、同−200meshのNi粉末、同
−200meshのCo粉末、同−200meshのFe−Mo合
金(Mo:60%含有)粉末、および同−200mesh
のFe−W合金(W:75%含有)粉末を用意し、
これら原料粉末を第2表に示される配合組成に配
合し、混合し6ton/cm2の圧力で圧粉体に成形し、
ついで水素雰囲気中、温度:1170℃に1時間保持
して焼結し、さらに、この結果得られた焼結体上
に、それぞれ第2表に示される量(全体割合量)
のCuが含浸されるように、所定量のCu粉末をの
せ、アンモニア分解ガス中、温度:1130℃に30分
間保持の条件でCu溶浸処理を施した後、直ちに
このCu溶浸処理温度より油焼入れし、引続いて
実施例1における本発明弁座1〜22と同一の条件
でサブゼロ処理および焼戻し処理を行なうことに
よつて、上記の配合組成およびCu含浸量と実質
的に同一の最終成分組成をもつた本発明弁座23〜
40をそれぞれ製造した。[Table] For the purpose of comparison, the same manufacturing conditions as the above-mentioned valve seat of the present invention were used, except that one of the constituent components had a composition outside the scope of the present invention, as shown in Table 1. Comparative valve seats 1 to 6 were manufactured under the following conditions. Furthermore, as shown in Table 1, the quenching temperature,
Comparative valve seats 7 to 11 were manufactured under the same manufacturing conditions as the valve seat 2 of the present invention described above, except that either the sub-zero treatment temperature or the tempering treatment temperature was outside the scope of the present invention. Note that in Table 1, conditions that are outside the scope of the present invention are marked with * regarding these comparative valve seats 1 to 11. Next, Rockwell hardness was measured for the resulting valve seats 1 to 22 of the present invention and comparative valve seats 1 to 11, and valve material: austenitic steel, valve temperature: 900°C, valve lift amount: 6.8 mm, Valve seat temperature:
350℃, seating load: 40Kg, rotation speed: 3000r.pm
(A wear resistance test was conducted under the conditions of atmosphere: LPG combustion gas and test time: 50 hours to determine the wear resistance of the valve and valve seat. These measurement results are shown in Table 1. The above-mentioned valve seats 1 to 22 of the present invention and comparative valve seats 1 to 11 were made of head material: FC20 (cast iron) and
AC5A (A alloy), press-fit surface head dimensions: 44.00±
0.01mm, press-fit face valve seat dimensions: 44.1±0.01mm, press-fit allowance: 100μm, head dimensions: 44mmφ×90mmφ×2.0
mm, valve seat dimensions: 44.1mmφ x 34mmφ x 8mm, press-fit load: 800 to 1000Kg (for cast iron head) and
1000 to 1300 kg (in case of A alloy head), fit and install on cast iron head and A alloy head, heat and hold in the atmosphere at 500℃ for 10 hours, and then remove the valve seat from the head. The extraction load of each was measured. The measurement results are also shown. As is clear from the results shown in Table 1, in the common valve seats 1 to 11 in which any of the conditions is outside the scope of the present invention, at least any of the wear resistance, attack resistance, and extraction load On the other hand, valve seats 1 to 22 of the present invention all have excellent wear resistance, are less likely to attack others, and have an extremely large extraction load. It's getting old. Example 2 As raw material powders, Fe powder with a particle size of -100mesh, Fe-Cr alloy (containing Cr: 12%) powder with a particle size of -100mesh, carbon powder with a particle size of -100mesh, and -
100mesh Cu powder, -200mesh Ni powder, -200mesh Co powder, -200mesh Fe-Mo alloy (Mo: 60% content) powder, and -200mesh
Prepare Fe-W alloy (containing 75% W) powder,
These raw material powders were blended into the composition shown in Table 2, mixed, and molded into a green compact at a pressure of 6 tons/cm 2 .
Then, in a hydrogen atmosphere, the temperature was maintained at 1170°C for 1 hour for sintering, and the amounts shown in Table 2 (total percentage amounts) were added to the resulting sintered body.
A predetermined amount of Cu powder is placed on top so that the Cu powder is impregnated, and Cu infiltration treatment is performed in ammonia decomposition gas at a temperature of 1130℃ for 30 minutes. By oil quenching, followed by sub-zero treatment and tempering treatment under the same conditions as the valve seats 1 to 22 of the present invention in Example 1, a final product with substantially the same composition and Cu impregnation amount as described above was obtained. Valve seat of the present invention having a component composition 23~
40 were produced each.
【表】
この結果得られた本発明弁座23〜40について、
実施例1におけると同一の条件で、硬さ、摩耗
量、および抜出荷重を測定し、この測定結果を第
2表に合せて示した。
第2表に示されるように、本発明弁座23〜40に
おいても本発明弁座1〜22の場合と同様に、すぐ
れた耐摩耗性、きわめて小さな相手攻撃性、さら
に大きな抜出荷重が得られることが明らかであ
る。
上述のように、この発明のFe基焼結合金製弁
座は、残留オーステナイトが存在しない、安定な
微細マルテンサイト組織を有するので、すぐれた
耐摩耗性をもつと共に、相手材たる弁を損傷する
こともなく、さらに熱的影響を全く受けない安定
した組織をもつので、使用中にヘツドから脱落す
ることもないなど工業上有用な特性をもつもので
ある。[Table] Regarding the valve seats 23 to 40 of the present invention obtained as a result,
Hardness, wear amount, and extraction load were measured under the same conditions as in Example 1, and the measurement results are shown in Table 2. As shown in Table 2, the valve seats 23 to 40 of the present invention also have excellent wear resistance, extremely low attack resistance, and a large extraction load, similar to the valve seats 1 to 22 of the present invention. It is clear that As mentioned above, the Fe-based sintered alloy valve seat of the present invention has a stable fine martensitic structure with no residual austenite, so it has excellent wear resistance and does not damage the mating material of the valve. Moreover, since it has a stable structure that is completely unaffected by heat, it has industrially useful properties such as not falling off from the head during use.
Claims (1)
30%を含有し、残りがFeと不可避不純物からな
る組成(以上重量%)を有する焼結体またはCu
含浸焼結体を、900〜1200℃の温度から焼入れ
し、−20℃以下の温度でサブゼロ処理し、引続い
て400〜700℃の温度で焼戻し処理することを特徴
とするFe基焼結合金製弁座の製造法。 2 C:0.5〜1.5%、Cr:1〜10%、Cu:1〜
30%を含有し、さらにNiおよびCuのうちの1種
または2種:1〜15%を含有し、残りがFeと不
可避不純物からなる組成(以上重量%)を有する
焼結体またはCu含浸焼結体を、900〜1200℃の温
度から焼入れし、−20℃以下の温度でサブゼロ処
理し、引続いて400〜700℃の温度で焼戻し処理す
ることを特徴とするFe基焼結合金製弁座の製造
法。 3 C:0.5〜1.5%、Cr:1〜10%、Cu:1〜
30%を含有し、さらにMoおよびWのうちの種ま
たは2種:1〜15%を含有し、残りがFeと不可
避不純物からなる組成(以上重量%)を有する焼
結体またはCu含浸焼結体を、900〜1200℃の温度
から焼入れし、−20℃以下の温度でサブゼロ処理
し、引続いて400〜700℃の温度で焼戻し処理する
ことを特徴とするFe基焼結合金製弁座の製造
法。 4 C:0.5〜1.5%、Cr:1〜10%、Cu:1〜
30%を含有し、さらにNiおよびCoのうちの1種
または2種:1〜1.5%と、MoおよびWのうちの
1種または2種:1〜15%とを含有し、残りが
Feと不可避不純物からなる組成(以上重量%)
を有する焼結体またはAu含浸焼結体を、900〜
1200℃の温度から焼入れし、−20℃以下の温度で
ザブゼロ処理し、引続いて400〜700℃の温度だ焼
戻し処理することを特徴とするFe基焼結合金製
弁座の製造法。[Claims] 1 C: 0.5-1.5%, Cr: 1-10%, Cu: 1-1
A sintered body or Cu having a composition (more than 30% by weight) with the remainder consisting of Fe and unavoidable impurities.
An Fe-based sintered alloy characterized in that the impregnated sintered body is quenched at a temperature of 900 to 1200°C, subjected to sub-zero treatment at a temperature of -20°C or less, and subsequently tempered at a temperature of 400 to 700°C. Manufacturing method for valve seats. 2 C: 0.5~1.5%, Cr: 1~10%, Cu: 1~
A sintered body or a Cu-impregnated sintered body having a composition (weight %) containing 1 to 15% of one or two of Ni and Cu, and the remainder consisting of Fe and unavoidable impurities. A valve made of Fe-based sintered alloy, characterized in that the body is quenched at a temperature of 900 to 1200°C, subjected to sub-zero treatment at a temperature of -20°C or less, and subsequently tempered at a temperature of 400 to 700°C. Manufacturing method for seats. 3 C: 0.5~1.5%, Cr: 1~10%, Cu: 1~
A sintered body or Cu-impregnated sintered body containing 30% of Mo and W, and 1 to 15% of one or two of Mo and W, with the remainder consisting of Fe and unavoidable impurities (weight %) A valve seat made of Fe-based sintered alloy, characterized in that the body is quenched at a temperature of 900 to 1200°C, subjected to sub-zero treatment at a temperature of -20°C or less, and subsequently tempered at a temperature of 400 to 700°C. manufacturing method. 4 C: 0.5~1.5%, Cr: 1~10%, Cu: 1~
30%, further contains one or two of Ni and Co: 1 to 1.5%, one or two of Mo and W: 1 to 15%, and the rest is
Composition consisting of Fe and unavoidable impurities (more than % by weight)
sintered body or Au-impregnated sintered body with
A method for manufacturing a valve seat made of an Fe-based sintered alloy, characterized by quenching at a temperature of 1200°C, subzero treatment at a temperature of -20°C or lower, and subsequent tempering treatment at a temperature of 400 to 700°C.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11438280A JPS5739104A (en) | 1980-08-20 | 1980-08-20 | Production of valve seat made of fe based sintered alloy |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP11438280A JPS5739104A (en) | 1980-08-20 | 1980-08-20 | Production of valve seat made of fe based sintered alloy |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5739104A JPS5739104A (en) | 1982-03-04 |
| JPS6140001B2 true JPS6140001B2 (en) | 1986-09-06 |
Family
ID=14636270
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP11438280A Granted JPS5739104A (en) | 1980-08-20 | 1980-08-20 | Production of valve seat made of fe based sintered alloy |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5739104A (en) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8921260D0 (en) * | 1989-09-20 | 1989-11-08 | Brico Engineering Company | Sintered materials |
| KR100492313B1 (en) * | 2002-01-22 | 2005-06-03 | 삼성전자주식회사 | Method of manufacturing sintered metal and flange of rotary compressor manufactured thereby |
| KR100461306B1 (en) * | 2002-06-21 | 2004-12-14 | 한국분말야금(주) | Wear resist sintering alloy for valve seat and method for manufacturing the same |
| DE102012013226A1 (en) * | 2012-07-04 | 2014-01-09 | Bleistahl-Produktions Gmbh & Co Kg | High heat conducting valve seat ring |
| JP5658804B1 (en) * | 2013-07-26 | 2015-01-28 | 株式会社リケン | Sintered alloy valve guide and manufacturing method thereof |
| CN103758746B (en) * | 2014-01-17 | 2015-10-28 | 钢铁研究总院 | A kind of steel-bimetal copper-steel rotor and manufacture method thereof |
| CN103757550B (en) * | 2014-01-17 | 2015-11-25 | 钢铁研究总院 | A kind of self-lubricating abrasion-resistant steel antifriction layer material and preparation method thereof |
| CN105586535B (en) * | 2015-12-28 | 2017-12-08 | 仪征市昌达粉末冶金制品有限公司 | Without cobalt-alloy material powder metallurgy valve seat and its preparation method and application |
-
1980
- 1980-08-20 JP JP11438280A patent/JPS5739104A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5739104A (en) | 1982-03-04 |
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