JPS6119759A - Abrasion resistant cast iron - Google Patents

Abrasion resistant cast iron

Info

Publication number
JPS6119759A
JPS6119759A JP13942884A JP13942884A JPS6119759A JP S6119759 A JPS6119759 A JP S6119759A JP 13942884 A JP13942884 A JP 13942884A JP 13942884 A JP13942884 A JP 13942884A JP S6119759 A JPS6119759 A JP S6119759A
Authority
JP
Japan
Prior art keywords
cast iron
wear
carbide
resistant cast
iron according
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
JP13942884A
Other languages
Japanese (ja)
Inventor
Masami Suzuki
鈴木 正実
Shigetoshi Sugimoto
杉本 繁利
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
Priority to JP13942884A priority Critical patent/JPS6119759A/en
Publication of JPS6119759A publication Critical patent/JPS6119759A/en
Pending legal-status Critical Current

Links

Abstract

PURPOSE:To provide the titled cast iron improved in abrasion resistance, which is constituted of a composition consisting of a specific amount of C, Si, Mn, Ni and Mo, one or more of a carbide forming element selected from Cr, V, W, Nb and Ta and the remainder of Fe and inevitable impurities and has a bainite structure on which one or more of carbide of said carbide forming element is precipitated. CONSTITUTION:The titled cast iron has a composition consisting of, on a wt. basis, 2.4-3.4% C, 2.0-3.0% Si, 0.2-1.0% Mn, 0.5-1.5% Ni, 1.0-2.0% Mo, 0.3-2.0% of one or more of a carbide forming element selected from Cr, V, W, Nb and Ta and the remaider of Fe and inevitable impurities. The structure of said cast iron is based on bainite formed by cast and one or more of Cr7C3, VC, WC and carbide based on Nb and Ta is precipitated thereon. By this constitution, cast iron more enhanced in abrasion resistance and suitable for the intake valve seat used in the dynamic valve mechanism of the internal-combustion engine of an automobile is obtained.

Description

【発明の詳細な説明】 [産業上の利用分野] 本発明は耐摩耗性鋳鉄に関する。本発明は、自動車の内
燃機関の動弁機構で用いられるインテークバルブシート
やバルブガイド等に利用することができる。ここでイン
テークバルブシートは、混合ガスを吸入する側のバルブ
を保持するシートであり、バルブが着脱することでガス
をシールする。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to wear-resistant cast iron. INDUSTRIAL APPLICATION This invention can be utilized for an intake valve seat, a valve guide, etc. used in the valve train of the internal combustion engine of an automobile. Here, the intake valve seat is a seat that holds a valve on the side that sucks in mixed gas, and seals the gas by attaching and detaching the valve.

[従来の技術] 例えば、自動車の内燃機関の動弁機構で使用されるイン
テークバルブシートは、従来より、耐摩耗性、潤滑性、
価格等を考慮して鋳鉄や焼結合金から作製されている。
[Prior Art] For example, intake valve seats used in the valve train of an automobile's internal combustion engine have traditionally had wear resistance, lubricity,
It is manufactured from cast iron or sintered alloy in consideration of cost and other factors.

ところで、近年、熱効率の向上、出力の増大等の要請か
ら、過給機付きエンジン、1気筒複数パルプエンジン等
が開発され、内燃機関はより高性能化しつつある。この
ように内燃機関が高性能化しつつあるといった情況を鑑
みると、従来がら使用されている鋳鉄や焼結合金では耐
摩耗性が不足する。そのため耐摩耗性を一層向上させる
必要性が大きくなっている。
Incidentally, in recent years, in response to demands for improved thermal efficiency, increased output, etc., engines with superchargers, single-cylinder multiple pulp engines, etc. have been developed, and internal combustion engines are becoming more efficient. In view of the fact that the performance of internal combustion engines is increasing, the wear resistance of conventionally used cast iron and sintered alloys is insufficient. Therefore, there is an increasing need to further improve wear resistance.

[発明が解決しようとする問題点] 本発明は、上記した実情に鑑みなされたものであり、耐
摩耗性を改良した耐摩耗性鋳鉄を提供することをも目的
とする。
[Problems to be Solved by the Invention] The present invention has been made in view of the above-mentioned circumstances, and it is also an object of the present invention to provide a wear-resistant cast iron with improved wear resistance.

[問題点を解決するための手段コ 本発明に係る耐摩耗性鋳鉄は、重量%で炭素2゜4〜3
.4%、ケイ素2.0〜3.0%、マンガン0.2〜1
.0%、ニッケル0.5〜1.5%、モリブデン1.0
〜2.0%、クロム、バナジウム、タングステン、ニオ
ブ及びタンタルの1種または2種以上の炭化物形成元素
0.3〜2.0%、残部鉄、不可避の不純物からなる組
成の鋳鉄であって、その組織は、鋳放しで形成されたベ
イナイトを主体どし、 クロム炭化物、バナジウム炭化物、タングステン炭化物
、ニオブとタンタルを主体とする炭化物のうち、少なく
とも一種を有することを特徴とするものである。
[Means for solving the problem] The wear-resistant cast iron according to the present invention has a carbon content of 2°4 to 3% by weight.
.. 4%, silicon 2.0-3.0%, manganese 0.2-1
.. 0%, nickel 0.5-1.5%, molybdenum 1.0
~2.0%, one or more carbide-forming elements of chromium, vanadium, tungsten, niobium, and tantalum 0.3 to 2.0%, the balance iron, and unavoidable impurities. Its structure is mainly composed of bainite formed in as-cast conditions, and is characterized by having at least one of chromium carbide, vanadium carbide, tungsten carbide, and carbide mainly composed of niobium and tantalum.

本発明に係る耐摩耗性鋳鉄の組織は、ベイナイトを主体
とする。ベイナイトは通常、適冷オーステナイトに恒温
変態等の熱処理を施したときに生じるが、本発明に係る
耐摩耗性鋳鉄では、熱処理を施すことなく鋳放しのまま
でベイナイトとする。
The structure of the wear-resistant cast iron according to the present invention is mainly composed of bainite. Bainite is normally produced when properly cooled austenite is subjected to heat treatment such as isothermal transformation, but in the wear-resistant cast iron according to the present invention, bainite is produced as-cast without any heat treatment.

組織をベイナイトとしたのは、主として、耐摩耗性、強
度、靭性などを改善するためである。ベイナイト中には
通常、黒鉛が生じている。黒鉛は潤滑性を確保する役割
を果す。黒鉛の形状は一般的に片状である。黒鉛の大き
さは、粗大化していないものがよく、一般には30〜1
20μ程度が望ましい。組織中には、クロムの炭化物、
バナジウムの炭化物、タングステンの炭化物、ニオブと
タンタルを主体とする炭化物のうち、一種類の炭化物が
析出している。場合によっては上記炭化物のうち二種以
上を析出させてもよい。本発明で生じる炭化物は、一般
的には複炭化物であり、硬さは通常f−1v1800〜
2800である。クロムの炭化物としては一般にM7C
3型であり、バナジウム、タングステン、ニオブとタン
タルを主体とする炭化物は一般にMC型である。これら
の炭化物は、該表面にもあられれ、耐摩耗性に寄与する
The reason why the structure is bainite is mainly to improve wear resistance, strength, toughness, etc. Graphite usually occurs in bainite. Graphite plays a role in ensuring lubricity. The shape of graphite is generally flaky. The size of the graphite is preferably one that is not coarse, and is generally 30 to 1
A thickness of about 20μ is desirable. The structure contains chromium carbide,
One type of carbide is precipitated out of vanadium carbide, tungsten carbide, and carbide mainly composed of niobium and tantalum. In some cases, two or more of the above carbides may be precipitated. The carbide produced in the present invention is generally a double carbide, and the hardness is usually f-1v1800 ~
It is 2800. The carbide of chromium is generally M7C.
3 type, and carbides mainly composed of vanadium, tungsten, niobium, and tantalum are generally MC type. These carbides are also present on the surface and contribute to wear resistance.

次に組成の限定理由についてのべる。Next, we will discuss the reasons for limiting the composition.

炭素は黒鉛を生じさせるため、チル化傾向を抑えるため
、又、上記炭化物を生じさせるために必要である。炭素
を2.4〜3.4%としたのは、2.4%より少ないと
チル化傾向が増すため、黒鉛生成上好ましくなく、3.
4%を越えると黒鉛が粗大化して硬さが低下するため好
ましくないからである。
Carbon is necessary to form graphite, to suppress the tendency to chill, and to form the carbides mentioned above. The reason why the carbon content is 2.4 to 3.4% is because if it is less than 2.4%, the tendency to chill increases, which is not preferable in terms of graphite formation.
This is because if it exceeds 4%, graphite becomes coarse and hardness decreases, which is not preferable.

ケイ素を2.0〜3.0%としたのは、2.0%より少
ないとチル化傾向が増すため黒鉛生成上好ましくなく、
3.0%を越えると黒鉛が粗大化して硬さが低下するた
め好ましくないからである。
The reason why silicon is set at 2.0 to 3.0% is that if it is less than 2.0%, the tendency to chill increases, which is not preferable in terms of graphite formation.
This is because if it exceeds 3.0%, graphite becomes coarse and hardness decreases, which is not preferable.

fマンガンを0.2〜1.0%としたのは、0゜2%よ
り少ないと不可避の不純物であるSの有害性を除去でき
ず、1.0%を越えるとチル化傾向が増して黒鉛生成上
好ましくないからである。
The reason for setting f-manganese to 0.2 to 1.0% is that if it is less than 0.2%, the harmfulness of S, which is an unavoidable impurity, cannot be removed, and if it exceeds 1.0%, the tendency to chill increases. This is because it is unfavorable in terms of graphite formation.

ニッケルとモリブデンは主として、組織を鋳放しのまま
でベイナイト化する役割を果す。ニッケルを0.5〜1
.5%としたのは、又モリブデンを1.0〜2.0%と
したのは、鋳放しのままで、組織をベイナイト化するた
めである。
Nickel and molybdenum primarily serve to bainitize the as-cast structure. 0.5-1 nickel
.. The reason why the molybdenum content is 5% and the molybdenum content is 1.0 to 2.0% is to convert the structure into bainite in the as-cast state.

炭化物形成元素のうち、クロムのみを含む場合には、ク
ロムは0.3〜1.0%であることが望ましい。この場
合には、鋳放しのままのベイナイトにクロムの複炭化物
が析出する。
When only chromium is included among the carbide-forming elements, the content of chromium is preferably 0.3 to 1.0%. In this case, double carbide of chromium is precipitated in the as-cast bainite.

炭化物形成元素のうち、バナジウムのみを含む場合には
、バナジウムは0.3〜1.0%であることが望ましい
。この場合には、鋳放しのままのベイナイトにバナジウ
ムの複炭化物が析出する。
When only vanadium is included among the carbide-forming elements, the content of vanadium is preferably 0.3 to 1.0%. In this case, double carbide of vanadium is precipitated in the as-cast bainite.

炭化物形成元素のうちタングステンのみを含む場合には
、タングステンは0.3〜1.0%であることが望まし
い。この場合には、鋳放しのままのベイナイトにタング
ステンの炭化物が析出する。
When only tungsten is included among the carbide-forming elements, the content of tungsten is preferably 0.3 to 1.0%. In this case, tungsten carbide precipitates in the as-cast bainite.

クロム、バナジウム、タングステンを上記含有量とした
理由は、0.3%よりも少ない複炭化物を形成しノにく
いし、1.0%を越えるとチル化傾向が大きくなり好ま
しくないからである。
The reason why the content of chromium, vanadium, and tungsten is set as above is that it is difficult to form double carbides when the content is less than 0.3%, and when it exceeds 1.0%, the tendency to chill increases, which is not preferable.

本発明に係る耐摩耗性鋳鉄を製造するにあたっては、溶
解温度は1350〜1650℃、注湯温度は1250〜
1550℃、鋳物の断面肉厚は5−15mmとすること
ができる。
In producing the wear-resistant cast iron according to the present invention, the melting temperature is 1350-1650°C, and the pouring temperature is 1250-1650°C.
At 1550°C, the cross-sectional thickness of the casting can be 5-15 mm.

[発明の効果〕 本発明に係る耐摩耗性鋳鉄は、後述する試験例で示すよ
うに当り幅増加量、摩耗痕面積ともに小さく、耐摩耗性
が従来品に比して向上している。
[Effects of the Invention] As shown in the test examples described below, the wear-resistant cast iron according to the present invention has a small increase in contact width and a small wear scar area, and has improved wear resistance compared to conventional products.

従ってバルブシート、バルブガイド等に用いられる耐摩
耗材料として好適する。
Therefore, it is suitable as a wear-resistant material for use in valve seats, valve guides, etc.

[試験例1] まず、自動車の内燃機関の動弁機構で用いられるインテ
ークバルブシートを、本発明に係る耐摩耗性鋳鉄、及び
比較材から作製した。バルブシートを作製した本発明に
係る耐摩耗性鋳鉄及び比較材の組成を第1表に示した。
[Test Example 1] First, intake valve seats used in the valve train of an internal combustion engine of an automobile were manufactured from wear-resistant cast iron according to the present invention and a comparative material. Table 1 shows the compositions of the wear-resistant cast iron according to the present invention and comparative materials from which valve seats were made.

第1表においてAlB、Cはそれぞれ比較材(従来より
バルブシートに用いられている材料)を示し、D、E、
F、Gはそれぞれ本発明材を示す。
In Table 1, AlB and C indicate comparative materials (materials conventionally used for valve seats), D, E,
F and G each indicate the materials of the present invention.

本発明に係る耐摩耗性鋳鉄でバルブシートを作製するに
あたっては、具体的には以下のようにして行なった。溶
解温度は1500℃、注湯温度は1400℃とし、外径
φ33、内径φ13、長さ1501RR1の円筒状粗材
を鋳造した。この粗材から所定形状のバルブ;−トを機
械加工にて作製した。
Specifically, a valve seat was manufactured using wear-resistant cast iron according to the present invention as follows. The melting temperature was 1500° C., the pouring temperature was 1400° C., and a cylindrical rough material with an outer diameter of φ33, an inner diameter of φ13, and a length of 1501 RR1 was cast. A valve of a predetermined shape was fabricated from this crude material by machining.

本試験では、具体的に上記インテークバルブシートをエ
ンジンに組み込み、6800rllll1150時間の
耐久試験を行なった。バルブシートの耐摩耗性は、該バ
ルブシートの当り幅増加量で測定した。ここで当り幅増
加邑とはバルブによってたたかれる面の巾の増加量の意
味である。試験結果を第1表に示す。
In this test, the above-mentioned intake valve seat was specifically assembled into an engine, and a durability test of 6,800 rllll for 1,150 hours was conducted. The wear resistance of the valve seat was measured by the amount of increase in the contact width of the valve seat. Here, the term "increase in contact width" means the amount of increase in the width of the surface struck by the valve. The test results are shown in Table 1.

本発明材であるり、E、F、Gのそれぞれの当り幅増加
量は、0.18〜0.25ミリメートル程麿と少なかっ
た。特にクロムの炭化物が析出している試験片りが最も
小さく、耐摩耗性が向上していた。一方、比較材の当り
幅増加量は、0.33.0.45.0.64ミリメート
ルと大きかった。以上のことから本発明に係る耐摩耗性
鋳鉄では、従来品に比して、耐摩耗性が向上しているの
がわかる。
For the materials of the present invention, the increase in contact width for each of E, F, and G was as small as 0.18 to 0.25 mm. In particular, the test piece with precipitated chromium carbide was the smallest, showing improved wear resistance. On the other hand, the increase in contact width of the comparative material was as large as 0.33, 0.45, and 0.64 mm. From the above, it can be seen that the wear-resistant cast iron according to the present invention has improved wear resistance compared to conventional products.

なお、参考までに本発明材りの顕微鏡組織写真を第1図
に示す。大きな黒いすし状のものが炭素、中央下方およ
び左側下方のアメーバ状の白いものがクロムの炭化物、
細い白い結晶がベーナイトである。
For reference, a photograph of the microscopic structure of the material of the present invention is shown in FIG. The large black sushi-shaped substance is carbon, and the amoeba-shaped white substance in the lower center and lower left side is chromium carbide.
The thin white crystals are bainite.

[試験例2] まず本発明に係る耐摩耗性鋳鉄及び比較材で試料を作製
した。試験片の形状は板状であり、その大きさは、25
 X 60 x 5 amである。本発明に係る耐摩耗
性鋳鉄及び比較材の組成を第2表に示した。
[Test Example 2] First, samples were prepared using wear-resistant cast iron according to the present invention and a comparative material. The shape of the test piece is a plate, and its size is 25
x 60 x 5 am. The compositions of the wear-resistant cast iron according to the present invention and comparative materials are shown in Table 2.

本発明に係る耐摩耗性鋳鉄で試料を作製するにあたって
は具体的には以下のようにして行なった。
Specifically, samples were prepared using the wear-resistant cast iron according to the present invention as follows.

溶解温度は1500℃、注湯温度は1400℃とし、1
50X150×101IIIIlの板状粗材を鋳造した
。この粗材から上記形状の試料を機械加工にて作製した
The melting temperature was 1500℃, the pouring temperature was 1400℃, and 1
A plate-shaped rough material measuring 50×150×101III1 was cast. A sample having the above shape was fabricated from this rough material by machining.

第2図に人感式摩擦摩耗試験の概略を示す。本試験では
、第2図に示すように、板状をなす試験片1に回転体2
を所定の荷重及びすべり速度で押しつりながら、所定の
距離摺動させた。そして試験片1の摺動向に形成された
摩耗痕面積の大きさで耐摩耗性を評価した。このときの
試験条件は、最終荷重6.3kg、すべり速度Q、3m
/5eC1すべり距離100mであり、回転体2はJI
s−suHi相当の耐熱鋼から作製した。
Figure 2 shows an outline of the human friction and wear test. In this test, as shown in FIG.
was slid for a predetermined distance while being pushed with a predetermined load and sliding speed. The wear resistance was evaluated based on the size of the wear scar area formed in the sliding movement of the test piece 1. The test conditions at this time were: final load 6.3 kg, sliding speed Q, 3 m.
/5eC1 sliding distance is 100m, and rotating body 2 is JI
It was made from heat-resistant steel equivalent to s-suHi.

試験結果を第3図に示す。第2図に示すように本発明材
の試験片Cr(e)〜試験片Cr(g)、試験片V(e
)〜試験片V(g)、試験片Nb(e)〜試験片Nb(
g>の場合には摩耗痕面積はいずれも15mm2以下の
値であった。一方比較材の摩耗痕面積は19mm2以上
と大きかった。
The test results are shown in Figure 3. As shown in FIG. 2, test pieces Cr(e) to Cr(g), test pieces V(e
) ~ test piece V (g), test piece Nb (e) ~ test piece Nb (
g>, the wear scar area was 15 mm2 or less in all cases. On the other hand, the wear scar area of the comparative material was as large as 19 mm2 or more.

このことからも、本発明に係る耐摩耗性鋳鉄は耐摩耗性
に優れていることがわかる。
This also shows that the wear-resistant cast iron according to the present invention has excellent wear resistance.

は摩擦摩耗試験を概略して示す側面図である。第3図は
摩擦摩耗試験の試験結果を示すグラフである。
FIG. 2 is a side view schematically showing a friction and wear test. FIG. 3 is a graph showing the results of the friction and wear test.

Claims (7)

【特許請求の範囲】[Claims] (1)重量%で炭素2.4〜3.4%、ケイ素2.0〜
3.0%、マンガン0.2〜1.0%、ニッケル0.5
〜1.5%、モリブデン1.0〜2.0%、クロム、バ
ナジウム、タングステン、ニオブ及びタンタルの1種ま
たは2種以上の炭化物形成元素0.3〜2.0%、残部
鉄、不可避の不純物からなる組成の鋳鉄であって、その
組織は、鋳放しで形成されたベイナイトを主体とし、 クロム炭化物、バナジウム炭化物、タングステン炭化物
、ニオブとタンタルを主体とする炭化物のうち、少なく
とも一種を有することを特徴とする耐摩耗性鋳鉄。
(1) Carbon 2.4-3.4%, silicon 2.0-2.0% by weight
3.0%, manganese 0.2-1.0%, nickel 0.5
~1.5%, molybdenum 1.0-2.0%, one or more carbide-forming elements of chromium, vanadium, tungsten, niobium and tantalum 0.3-2.0%, balance iron, unavoidable Cast iron with a composition consisting of impurities, whose structure is mainly composed of bainite formed in as-cast conditions, and has at least one of chromium carbide, vanadium carbide, tungsten carbide, and carbide mainly composed of niobium and tantalum. Wear-resistant cast iron.
(2)クロムは重量%で0.3〜1.0%である特許請
求の範囲第1項記載の耐摩耗性鋳鉄。
(2) The wear-resistant cast iron according to claim 1, wherein the chromium content is 0.3 to 1.0% by weight.
(3)バナジウムは重量%で0.3〜1.0%である特
許請求の範囲第1項記載の耐摩耗性鋳鉄。
(3) The wear-resistant cast iron according to claim 1, wherein vanadium is contained in an amount of 0.3 to 1.0% by weight.
(4)タングステンは重量%で0.3〜1.0%である
特許請求の範囲第1項記載の耐摩耗性鋳鉄。
(4) The wear-resistant cast iron according to claim 1, wherein the content of tungsten is 0.3 to 1.0% by weight.
(5)ニオブ及びタンタルの合計は、重量で0.8〜2
.0%である特許請求の範囲第1項記載の耐摩耗性鋳鉄
(5) The total amount of niobium and tantalum is 0.8 to 2 by weight
.. 0% wear-resistant cast iron according to claim 1.
(6)JIS−SUH1相当の耐熱鋼から作製した回転
体を荷重6.3kgで押しつけて、すべり速度0.3m
/secで100m摺動させたとき、摩耗痕面積は、1
5mm^2以下である特許請求の範囲第1項記載の耐摩
耗性鋳鉄。
(6) A rotating body made of heat-resistant steel equivalent to JIS-SUH1 is pressed with a load of 6.3 kg, and the sliding speed is 0.3 m.
/sec when sliding 100m, the wear scar area is 1
The wear-resistant cast iron according to claim 1, which has a thickness of 5 mm^2 or less.
(7)自動車の内燃機関の動弁機構で用いられるインテ
ークバルブシートに使用される特許請求の範囲第1項記
載の耐摩耗性鋳鉄。
(7) The wear-resistant cast iron according to claim 1, which is used for an intake valve seat used in a valve train of an internal combustion engine of an automobile.
JP13942884A 1984-07-05 1984-07-05 Abrasion resistant cast iron Pending JPS6119759A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP13942884A JPS6119759A (en) 1984-07-05 1984-07-05 Abrasion resistant cast iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP13942884A JPS6119759A (en) 1984-07-05 1984-07-05 Abrasion resistant cast iron

Publications (1)

Publication Number Publication Date
JPS6119759A true JPS6119759A (en) 1986-01-28

Family

ID=15244963

Family Applications (1)

Application Number Title Priority Date Filing Date
JP13942884A Pending JPS6119759A (en) 1984-07-05 1984-07-05 Abrasion resistant cast iron

Country Status (1)

Country Link
JP (1) JPS6119759A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63166929A (en) * 1986-12-22 1988-07-11 フォード モーター カンパニー Production of gray cast iron having increased abrasion resistance and toughness
WO1997032049A1 (en) * 1996-02-28 1997-09-04 Kabushiki Kaisha Riken Cast iron and piston ring

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63166929A (en) * 1986-12-22 1988-07-11 フォード モーター カンパニー Production of gray cast iron having increased abrasion resistance and toughness
WO1997032049A1 (en) * 1996-02-28 1997-09-04 Kabushiki Kaisha Riken Cast iron and piston ring
US5972128A (en) * 1996-02-28 1999-10-26 Kabushiki Kaisha Riken Cast iron and piston ring
KR100260348B1 (en) * 1996-02-28 2000-07-01 오구찌 구니히코 Cast iron and piston ring
CN1064719C (en) * 1996-02-28 2001-04-18 株式会社理研 Cast iron and piston ring

Similar Documents

Publication Publication Date Title
US4929419A (en) Heat, corrosion, and wear resistant steel alloy and article
US4268309A (en) Wear-resisting sintered alloy
WO2009122985A1 (en) Iron-base sintered alloy for valve sheet and valve sheet for internal combustion engine
US4778522A (en) Wear resistant iron-base sintered alloy
US5019332A (en) Heat, corrosion, and wear resistant steel alloy
US5221321A (en) Fe-base sintered alloy for valve seats for use in internal combustion engines
EP0668367A1 (en) Heat-resistant, austenitic cast steel and exhaust equipment member made thereof
KR890002282B1 (en) Co base alloy for engine valve and engine valve sheet
US5194220A (en) Austenitic cast steel and articles made thereof
US20030188808A1 (en) Thermal fatigeue resistant cast steel
US20080112815A1 (en) Blade Mounting Ring For A Turbocharger On An Internal Combustion Engine
EP0359085B1 (en) Heat-resistant cast steels
JPH0610321B2 (en) Abrasion resistant sintered alloy
JPS6119759A (en) Abrasion resistant cast iron
KR20030055751A (en) Cast iron with improved oxidation resistance at high temperature
US4948556A (en) Piston ring material and piston ring
JP2706561B2 (en) Valve seat material for internal combustion engine and method of manufacturing the same
US4218243A (en) Fully martensitic steel for a metal mold for molding glass and the metal mold
JPH05230596A (en) Piston ring material
JP2866868B2 (en) Piston ring material
JP3440008B2 (en) Sintered member
JPS60138050A (en) Corrosion and wear resistant cast iron
EP4190931A1 (en) Nickel-niobium intermetallic alloy useful for valve seat inserts
JP2594505B2 (en) Rocker arm
JPS58120756A (en) Ni alloy for valve and valve sheet of internal combustion engine