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JPS5910988B2 - Spheroidal graphite cast iron and its manufacturing method - Google Patents

Spheroidal graphite cast iron and its manufacturing method

Info

Publication number
JPS5910988B2
JPS5910988B2 JP54161365A JP16136579A JPS5910988B2 JP S5910988 B2 JPS5910988 B2 JP S5910988B2 JP 54161365 A JP54161365 A JP 54161365A JP 16136579 A JP16136579 A JP 16136579A JP S5910988 B2 JPS5910988 B2 JP S5910988B2
Authority
JP
Japan
Prior art keywords
cast iron
spheroidal graphite
graphite cast
content
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.)
Expired
Application number
JP54161365A
Other languages
Japanese (ja)
Other versions
JPS5594459A (en
Inventor
ホルスト・ミユ−ルバ−ガ−
ブルノ−・プリンツ
ボルフ・ブンデル
ウルリツヒ・シエ−フア−
ジヨゼフ・ボグナ−
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Individual
Original Assignee
Individual
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Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
    • C21D5/00Heat treatments of cast-iron
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C37/00Cast-iron alloys
    • C22C37/04Cast-iron alloys containing spheroidal graphite

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  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Refinement Of Pig-Iron, Manufacture Of Cast Iron, And Steel Manufacture Other Than In Revolving Furnaces (AREA)
  • Heat Treatment Of Articles (AREA)

Description

【発明の詳細な説明】 本発明、オーステナイトとペイナイトとの混合組織を有
する球状黒鉛鋳鉄及びその製造方法(%に対応する熱処
理及び冷却工程を有する方法)に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a spheroidal graphite cast iron having a mixed structure of austenite and paynite, and a method for manufacturing the same (a method having heat treatment and cooling steps corresponding to %).

この種の基礎組織を有する球状黒鉛鋳鉄及びその機械的
特性は、通常の使用範囲は別として、構造用材料として
も適している。
Spheroidal graphite cast iron with a basic structure of this type and its mechanical properties are suitable, apart from its normal use, as a structural material.

この材料はこれ迄専ら使用さfてきた精鋼を含み、自動
車モータ用クランク軸、流体力・じ取装置用セグメント
軸及びピストン、LKW−関節連結クラッチ用牽引連結
ジャーナル、自動車たわみ軸用たわみ軸頭部、トレーラ
クラッチ用クラッチ体等の構造用材料として適している
This material includes refined steel that has hitherto been used exclusively for crankshafts for automobile motors, segment shafts and pistons for fluid power steering devices, traction coupling journals for LKW-articulated clutches, and flexible shaft heads for automobile deflection shafts. It is suitable as a structural material for clutch bodies for trailer clutches, etc.

球状黒鉛鋳鉄の中で、高硬度の耐摩耗性材料としてペイ
ナイト組織全有する種類のものが古ぐ刀・ら知らnてお
り、使用さnてきた。
Among spheroidal graphite cast irons, those having a complete payinite structure as a highly hard and wear-resistant material are known from ancient times and have been used.

この場合、一般に鋳物の製造に際して920−950℃
のオーステナイト化湛度[2〜5分間保持するが、これ
によってマトリックスがほぼ均一な炭素含有量全有する
ようになり、或いは場合によっては鋳造後に存在するレ
デブリットが分解する。
In this case, generally 920-950℃ is used when manufacturing castings.
The austenitizing impregnation [held for 2 to 5 minutes, which ensures that the matrix has an almost uniform overall carbon content, or in some cases decomposes the redebrit present after casting.

オーステナイト化後に鋳物全急冷して、等温的なペイナ
イト変態飄度に達する前にオーステナイトのパーライ}
化k防いでいる。
After austenitization, the casting is completely rapidly cooled, and the austenite is pearlized before reaching the isothermal payinite transformation degree.
Preventing damage.

ペイナイト反応が終了する迄、鋳物?その飄度に保持し
、しかる後に通常通り室飄に冷却するしギーセライ(G
ie−βerei)6臣(1978)扁4、73〜80
頁〕。
Casting until the paynight reaction ends? It is maintained at that temperature, and then cooled to room temperature as usual.
ie-βerei) 6 Omi (1978) Bi 4, 73-80
page〕.

ペイナイト組織全有する別の球状黒鉛鋳鉄として知られ
ているものは、合金鋳鉄を出発材料とし、鋳造プロセス
に続く冷却段階に直接関連して、鋳物の厚みを目的とす
る量のニッケル、モリブデン、銅、場合によってはクロ
ム、マンガンによるペイナイト反応が生じる(ドイツ連
邦共和国出願公開第1808515号)。
Another type of cast iron, known as spheroidal graphite cast iron, which has a full paynitic structure, uses an alloyed cast iron as a starting material and, in direct connection with the cooling step that follows the casting process, the thickness of the casting is adjusted to the desired amount of nickel, molybdenum, and copper. In some cases, a payinite reaction occurs due to chromium and manganese (German Published Application No. 1808515).

ドイツ連邦共和国出願公開第2334992号によれば
、通常の量の炭素、シリコン、リン、イオウ及びマグネ
シウムと、0.10〜0.26%のモリブデンと0.3
〜1.4%のマンガンとを含有する低合金球状黒鉛鋳鉄
が公知となっている。
According to DE-A-2334992, conventional amounts of carbon, silicon, phosphorus, sulfur and magnesium, 0.10-0.26% molybdenum and 0.3%
Low alloy spheroidal graphite cast irons containing ~1.4% manganese are known.

これから得られる鋳物は900℃のオーステナイト化温
度に加熱し、しかる後に300℃の浴中で2時間保持し
てから10分〜4時間で冷却する。
The resulting castings are heated to an austenitizing temperature of 900 DEG C. and then kept in a 300 DEG C. bath for 2 hours before being cooled for 10 minutes to 4 hours.

この方法ではオーステナイトーベイナイト組織が形成さ
れるために、10%の伸び率、270〜3 00HBの
硬度が得られる。
In this method, an austenite-bainite structure is formed, so that an elongation rate of 10% and a hardness of 270 to 300 HB can be obtained.

また、特開昭53−48015号公報には、球状黒鉛の
外に少なくとも5容量%の残留オーステナイト、残部か
主としてペイナイトである顕微鏡組織を有するノジュラ
ー鋳鉄が記載されている。
Furthermore, JP-A-53-48015 describes nodular cast iron having a microscopic structure consisting of at least 5% by volume of retained austenite in addition to spheroidal graphite, with the remainder being mainly paynite.

この鋳鉄は摩擦による伝動用の金属機械部品に使用する
のを目的とするものであって、それまでのかかる金属機
械部品の最大の欠点である高摩耗と低い摩擦抵抗性を改
善するものである。
This cast iron was intended to be used in metal mechanical parts for transmission by friction, and was intended to improve the major drawbacks of such metal mechanical parts up to that time: high wear and low frictional resistance. .

またかかる鋳鉄は硬度が高いので機械加工後に、熱処理
が通常行なわnている。
Furthermore, since such cast iron has high hardness, heat treatment is usually performed after machining.

またその鋳鉄の代表例の組成は、鉄の外に例えば2.4
%C,1.5%Si,0.5%凧、0.05%P及び0
.1%S(何れも重量%)である。
In addition to iron, the typical composition of cast iron is, for example, 2.4
%C, 1.5%Si, 0.5%Kite, 0.05%P and 0
.. 1% S (all percentages by weight).

本発明は、オーステナイトーベイナイト混合組織を有す
る球状黒鉛鋳鉄及びその製造方法全、使用するのに有利
な材料価値を損うことなしに改良することを目的とする
The object of the present invention is to improve a spheroidal graphite cast iron having a mixed austenite-bainite structure and a method for producing the same without impairing the material's advantageous value for use.

この目的は、マンガン0.3%未満、モリブデン0.2
〜0.8%、銅0.1〜1.5%、ケイ素2.0〜3.
0係、炭素2.5〜3.9%、ニッケル3%以下及び残
部が実質的に鉄力・らなる球状黒鉛鋳鉄に係る本発明に
よって達成される。
The purpose is to use less than 0.3% manganese and 0.2% molybdenum.
~0.8%, copper 0.1-1.5%, silicon 2.0-3.
This is achieved by the present invention, which relates to spheroidal graphite cast iron consisting essentially of 0% carbon, 2.5 to 3.9% carbon, 3% or less nickel, and the remainder substantially iron.

この球状黒鉛鋳鉄はオーステナイトーベイナイト組織の
形成に適しており、その形成に際しては、上記組成の鋳
物材料を800〜860℃、望ましくは820〜830
℃のオーステナイト化温度に加熱して10〜60分間、
望ましくは10〜25分間その扁度を保持し、次いで2
分以内で350〜400℃、望ましくは約375℃に急
冷し、この湛度に約5〜60分間、望ましくは20〜2
5分間保持する。
This spheroidal graphite cast iron is suitable for forming an austenite-bainite structure, and when forming it, the casting material having the above composition is heated to 800 to 860°C, preferably 820 to 830°C.
heating to the austenitizing temperature of °C for 10 to 60 minutes;
Preferably hold the flatness for 10-25 minutes, then
Rapidly cool to 350-400°C, preferably about 375°C within minutes, and keep at this temperature for about 5-60 minutes, preferably 20-200°C.
Hold for 5 minutes.

しかる後、室篇に冷却する。この球状黒鉛鋳鉄の上記組
成において、マンガンの含有量か0.01〜0. 2
5 %、モリブデンの含有量が0.25〜0.4%、銅
の含有量が0.4〜0.6係、ケイ素の含有量が2.2
〜2.6%、炭素の含有量が2.5〜37%更には30
〜3.2係であるのが好ましい。
After that, it is cooled down to room temperature. In the above composition of this spheroidal graphite cast iron, the manganese content is 0.01 to 0. 2
5%, molybdenum content 0.25-0.4%, copper content 0.4-0.6%, silicon content 2.2%.
~2.6%, carbon content 2.5-37% and even 30
~3.2 is preferable.

次に、上記組成の限定理由を説明する。Next, the reasons for limiting the above composition will be explained.

尚、炭素及びケイ素の含有量についてぱ=般に知らtて
いる球状黒鉛鋳鉄と同じ範囲にあり、かつその限定理由
もよく知らnたものと同じである力・ら説明全省略する
The content of carbon and silicon is within the same range as that of generally known spheroidal graphite cast iron, and the reason for the limitation is also the same as that well known, so a complete explanation will be omitted.

マンガンの含有量’to.3%未満、好ましくは0.0
1〜0.25%とした理由は、マンガンの含有量が多す
ぎると鋳造構造中に(少くともその肉厚が小さい場合)
カーバイトが生成するからである。
Manganese content'to. Less than 3%, preferably 0.0
The reason for setting it at 1 to 0.25% is that if the content of manganese is too high, it will cause damage to the cast structure (at least when the wall thickness is small).
This is because carbide is generated.

カーバイドが生成しこれを融解しなけ汎ばならない場合
に比べ、本発明では約100℃低い温度で熱処理可能で
ある。
In the present invention, heat treatment can be performed at a temperature approximately 100° C. lower than when carbide is generated and must be melted.

この点から見れば理論上マンガンの含有量は少ないほど
好ましいが、実際にはマンガン全完全に除去することは
不可能であり、カーバイドが生成しない程度にマンガン
が含有されているのは差しつかえない。
From this point of view, the lower the manganese content, the better in theory, but in reality it is impossible to completely remove all manganese, and it is okay to contain manganese to the extent that carbide is not produced. .

また、上述した範囲f 含有3nているマンガンは鋳鉄
の強度を高める効果を有する。
Further, manganese in the above-mentioned range f 3n has the effect of increasing the strength of cast iron.

モリブデンの含有量は0.2〜0,8%好ましくは0.
25〜0.4%である。
The content of molybdenum is 0.2 to 0.8%, preferably 0.8%.
It is 25-0.4%.

モリブデンによってペイナイトの成長が特に肉厚が20
rrrInより大きい場合に安定化ざれ促進されること
か知られている。
Molybdenum inhibits the growth of paynite, especially when the wall thickness is 20
It is known that stabilization is promoted when the value is larger than rrrIn.

しかし、モリブデンの量が多すぎるとカーバイドが生ず
るので、従来モリブテンの量の上限は0.2%とされて
いた。
However, if the amount of molybdenum is too large, carbide is generated, so the upper limit of the amount of molybdenum has conventionally been set at 0.2%.

本発明ではマンガンの量ヲ0.3%未満とすることによ
りカーバイドの生成が抑制さわることからモリプテンの
量’k 0. 2%より多くすることができるようにな
った。
In the present invention, the amount of molyptene 'k0. It is now possible to increase the rate to more than 2%.

その結果、通常2〜4%のニッケルが含有されている場
合にのみ可能であった肉厚が小さい場合のべイナイトー
オーステナイト構造の望ましい成長も可能になった。
As a result, the desirable growth of a bainitic-austenitic structure is also possible in the case of small wall thicknesses, which was normally only possible with a 2-4% nickel content.

モリプテンはiたパーライトの生成を防ぐという特異な
効果を有する。
Molyptene has the unique effect of preventing the formation of pearlite.

この効果はニッケルのそれよりも非常に大きいため、少
量のモリブデン添加によって通常必要なニッケルを大部
分節約可能となり、モリプテンが高価であるにもかかわ
らずコストを低減できる。
This effect is much greater than that of nickel, so adding a small amount of molybdenum can largely save the normally required nickel, reducing costs despite the high cost of molybdenum.

ニッケルの含有量は3.0%以下である。The content of nickel is 3.0% or less.

ニッケルはパーライトの生成を防ぎオーステナイト、特
に熱処理後の鋳造物に30〜40%含有ざnるオーステ
ナイトの安定化効果を有する。
Nickel prevents the formation of pearlite and has a stabilizing effect on austenite, especially when it is contained in a cast product after heat treatment at 30 to 40%.

ニッケルの含有量は肉厚に依存するが、上述した効果は
3.0係で飽和に達し、それ以上ではコストが高くなる
ばかりである。
Although the nickel content depends on the wall thickness, the above-mentioned effect reaches saturation at a factor of 3.0, and if it exceeds that, the cost will only increase.

ニッケルの平均含有量は約100一以下の肉厚を有する
鋳造物では1.0〜1.5%である。
The average nickel content is 1.0-1.5% for castings with wall thicknesses of about 100 mm or less.

銅の含有量は0. 1〜1.5%、好ましくは04〜0
.6%である。
Copper content is 0. 1-1.5%, preferably 04-0
.. It is 6%.

銅は高温におけるペイナイトーオーステナイト構造の安
定化効果を有するが、含有量が小さすぎるとこの効果は
十分でなく、また太きすぎると組織間に望ましくない相
が形成される。
Copper has the effect of stabilizing the paynitic-austenite structure at high temperatures, but if the content is too small, this effect will not be sufficient, and if the content is too thick, undesirable phases will be formed between the structures.

実施例 1 下記の化学組成を有する鋳鉄を常法に従って作成した。Example 1 Cast iron having the following chemical composition was prepared according to a conventional method.

0 375% P 0.02%Si
2.65係 S (0.01%Mn
0.18% Mg 0.04%Ni
1.35% Mo O.35%C
u O.80% この鋳鉄を820℃で20分間加熱し、次いで2分以内
に375℃になるように急冷し、この湛度で20分間保
持しfc後、室幅に冷却した。
0 375% P 0.02%Si
Section 2.65 S (0.01%Mn
0.18% Mg 0.04% Ni
1.35% MoO. 35%C
uO. 80% This cast iron was heated at 820°C for 20 minutes, then rapidly cooled to 375°C within 2 minutes, held at this level for 20 minutes, fc, and then cooled to room width.

この鋳鉄の物性は次の通りであった。The physical properties of this cast iron were as follows.

降伏強さ 61 6N/rnA極限強さ
8 9 2 N/Fna伸び
148% ブリネル硬度 2 6 9 KpAnjt′゛
7代し”” 8 0 ft lbs( 室1n
)衝撃強さ 48.5 ft lbs (−40°F/−40℃) 実施例 2 実施例lと同様にして、下記化学組成を有する鋳鉄?作
成した。
Yield strength 61 6N/rnA ultimate strength
8 9 2 N/Fna elongation
148% Brinell hardness 2 6 9 KpAnjt'゛7th grade'' 80 ft lbs (chamber 1n
) Impact strength 48.5 ft lbs (-40°F/-40°C) Example 2 Cast iron having the following chemical composition was prepared in the same manner as in Example 1. Created.

C388 % p o.oio%Si
2.61% S O.007係Mn 0
.22% Mg 0.042%Ni 1.
47% Mo 0.35 %Cu
O.76% Cr O.03 %この鋳鉄
全実施例1と同様に熱処理した後冷却した。
C388% po. oio%Si
2.61% SO. 007 Section Mn 0
.. 22% Mg 0.042% Ni 1.
47%Mo 0.35%Cu
O. 76% CrO. 03% All of this cast iron was heat treated in the same manner as in Example 1 and then cooled.

この鋳鉄は次のような物性を有していた。降伏強さ
6 4 0N/m法極限強さ 9
8 3 NAnA伸び 13.9% ブリネル硬度 298Kp/2yj本発明により
得られる利点は、技術の現状に対し、熱処理に要する消
費が著しく少なくて済むことである。
This cast iron had the following physical properties. yield strength
6 4 0N/m method ultimate strength 9
8 3 NAnA elongation 13.9% Brinell hardness 298 Kp/2yj The advantage obtained by the present invention is that, compared to the state of the art, the consumption required for heat treatment is significantly lower.

しかもこれが、オーステナイトーベイナイト組織全有す
る球状黒鉛鋳鉄の良好な材料特性を損うことなしに達成
できることである。
Moreover, this can be achieved without impairing the good material properties of spheroidal graphite cast iron, which has an entirely austenite-bainite structure.

顕微鏡写真によnば、内添されたスフエロライトを有す
るペイナイトーオーステナイト組織が存在した本発明に
よる球状黒鉛鋳鉄の磨面が示ざnた。
The micrograph shows a polished surface of the spheroidal graphite cast iron according to the present invention in which a paynitic-austenite structure with internally added spherolite was present.

t:(7)写Jノ黒い丸い部分が黒鉛ノジュールを示し
、そして暗い針状部分がペイナイトを、明るい組織成分
がオーステナイトヲ夫々示している。
t: (7) In photo J, the black round parts indicate graphite nodules, the dark needle-shaped parts indicate paynite, and the bright structural components indicate austenite.

以上述べた本発明全要約すると次のようになる。The present invention described above can be summarized as follows.

対応する熱処理及び冷却によって製造された、オーステ
ナイトーベイナイト混合組織を有する球状黒鉛鋳鉄は、
使用に際して好適な材料価値を示す。
Spheroidal graphite cast iron with austenite-bainite mixed structure produced by corresponding heat treatment and cooling,
Shows suitable material values for use.

その製造に要する消費を減らすために、球状黒鉛鋳鉄が
通常の量の炭素、シリコン、リン、イオウ、マグネシウ
ムの池に、0−0.3%(但し、0%及び0.3%k含
まず)のマンガンを含有している。
In order to reduce the consumption required for its production, spheroidal graphite cast iron is added to a pond of normal amounts of carbon, silicon, phosphorus, sulfur, and magnesium at 0-0.3% (excluding 0% and 0.3%K). ) contains manganese.

Claims (1)

【特許請求の範囲】 1 オーステナイトとペイナイトとの混合組織を有する
球状黒鉛鋳鉄において、マンガン0.3%未満、モリプ
テン0.2〜0.8%、銅0.1〜1.5%、ケイ素2
.0〜3,0%、炭素2.5〜3.9%、ニッケル3%
以下及び残部が実質的に鉄からなることを特徴とする球
状黒鉛鋳鉄。 2 マンガンの含有量が0.01〜0.25%であるこ
とを特徴とする特許請求の範囲第1項に記載の球状黒鉛
鋳鉄。 3 モリブデンの含有量が0.25〜0.4%であるこ
と’k%徴とする特許請求の範囲第1項または第2項に
記載の球状黒鉛鋳鉄。 4 銅の含有量が0.4〜0.6%であることを特徴と
する特許請求の範囲第1項〜第3項のいずnか1項に記
載の球状黒鉛鋳鉄。 5 ケイ素の含有量が2.2〜2.6%であること全特
徴とする特許請求の範囲第1項〜第4項のいずnか1項
に記載の球状黒鉛鋳鉄。 6 炭素の含有量が3.0〜3.2%であることを特徴
とする特許請求の範囲第1項〜第5項のいずれか1項に
記載の球状黒鉛鋳鉄。 γ マンガン0.3%未満、モリブデン0.2〜0.8
係、銅0.1〜1.5%、ケイ素2,0〜3.0%、炭
素2.5〜3.9%、ニッケル3%以下及び残部が実質
的に鉄からなる球状黒鉛鋳鉄材料全800〜860℃で
10〜60分間熱処理してオーステナイト化し、次いで
2分以内で350〜400℃に急冷し、この扁度に約5
〜60分間保持すること全特徴とする球状黒鉛鋳鉄の製
造方法。 8 オーステナイト化を820〜830℃で10〜25
分間行い、次いで約375℃に急冷し、更にこの温度に
20〜25分間保持することを特徴とする特許請求の範
囲第7項に記載の球状黒鉛鋳鉄の製造方法。 9 球状黒鉛鋳鉄材料に0.01〜0.25%のマンガ
ンを含有させることを特徴とする特許請求の範囲第γ項
または第8項に記載の球状黒鉛鋳鉄の製造方法。 10 球状黒鉛鋳鉄材料に0525〜0.4%のモリ
プテン全含有させることk%徴とする特許請求の範囲第
7項〜第9項のいずnか1項に記載の球状黒鉛鋳鉄の製
造方法。 11 球状黒鉛鋳鉄材料に0.4〜0.6%の銅を含
有させることを特徴とする特許請求の範囲第7項〜第1
0項のいずれか1項に記載の球状黒鉛鋳鉄の製造方法。 12球状黒鉛鋳鉄材料に2.2〜2.6%のケイ素全含
有させることを特徴とする特許請求の範囲弟7項〜第1
1項のいずれか1項に記載の球状黒鉛鋳鉄の製造方法。 13球状黒鉛鋳鉄材料に3.0〜3.2%の炭素全含有
させることを特徴とする特許請求の範囲第7項〜第12
項のいずnか1項に記載の球状黒鉛鋳鉄の製造方法。
[Claims] 1 Spheroidal graphite cast iron having a mixed structure of austenite and paynite, less than 0.3% manganese, 0.2 to 0.8% molypten, 0.1 to 1.5% copper, 2 silicon
.. 0-3.0%, carbon 2.5-3.9%, nickel 3%
Spheroidal graphite cast iron characterized in that the following and the remainder essentially consist of iron. 2. Spheroidal graphite cast iron according to claim 1, wherein the manganese content is 0.01 to 0.25%. 3. Spheroidal graphite cast iron according to claim 1 or 2, characterized in that the content of molybdenum is 0.25 to 0.4%. 4. Spheroidal graphite cast iron according to any one of claims 1 to 3, characterized in that the copper content is 0.4 to 0.6%. 5. Spheroidal graphite cast iron according to any one of claims 1 to 4, characterized in that the silicon content is 2.2 to 2.6%. 6. Spheroidal graphite cast iron according to any one of claims 1 to 5, characterized in that the carbon content is 3.0 to 3.2%. γ Manganese less than 0.3%, molybdenum 0.2-0.8
All spheroidal graphite cast iron materials consisting of 0.1 to 1.5% copper, 2.0 to 3.0% silicon, 2.5 to 3.9% carbon, 3% or less nickel, and the balance substantially iron. It is heat-treated at 800-860°C for 10-60 minutes to austenitize, then rapidly cooled to 350-400°C within 2 minutes, and the degree of flatness is approximately 5
A method for producing spheroidal graphite cast iron characterized by holding for ~60 minutes. 8 Austenitization at 820-830℃ 10-25
8. The method for producing spheroidal graphite cast iron according to claim 7, characterized in that the process is carried out for 1 minute, then rapidly cooled to about 375°C, and further maintained at this temperature for 20 to 25 minutes. 9. The method for producing spheroidal graphite cast iron according to claim γ or 8, characterized in that the spheroidal graphite cast iron material contains 0.01 to 0.25% manganese. 10. The method for producing spheroidal graphite cast iron according to any one of claims 7 to 9, wherein the total molyptene content is 0525 to 0.4% in the spheroidal graphite cast iron material. . 11 Claims 7 to 1, characterized in that the spheroidal graphite cast iron material contains 0.4 to 0.6% copper.
The method for producing spheroidal graphite cast iron according to any one of item 0. 12 Claims 7 to 1, characterized in that the spheroidal graphite cast iron material has a total silicon content of 2.2 to 2.6%
The method for producing spheroidal graphite cast iron according to any one of Item 1. 13 Claims 7 to 12, characterized in that the spheroidal graphite cast iron material has a total carbon content of 3.0 to 3.2%.
A method for producing spheroidal graphite cast iron according to any one of item n or 1.
JP54161365A 1978-12-13 1979-12-12 Spheroidal graphite cast iron and its manufacturing method Expired JPS5910988B2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19782853870 DE2853870A1 (en) 1978-12-13 1978-12-13 BALL GRAPHITE CAST IRON WITH AUSTENITIC-BAINITIC MIXED TEXTURE
DE28538707CBH 1978-12-13

Publications (2)

Publication Number Publication Date
JPS5594459A JPS5594459A (en) 1980-07-17
JPS5910988B2 true JPS5910988B2 (en) 1984-03-13

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Country Status (4)

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EP (1) EP0018445B2 (en)
JP (1) JPS5910988B2 (en)
DE (2) DE2853870A1 (en)
ZA (1) ZA796750B (en)

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JPS61264155A (en) * 1985-01-30 1986-11-22 Asahi Malleable Iron Co Ltd Spheroidal graphite cast iron having bainite matrix and its manufacture
JPH04333369A (en) * 1991-05-07 1992-11-20 Hitachi Zosen Corp Column welding equipment in structures

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JPS61264155A (en) * 1985-01-30 1986-11-22 Asahi Malleable Iron Co Ltd Spheroidal graphite cast iron having bainite matrix and its manufacture
JPH04333369A (en) * 1991-05-07 1992-11-20 Hitachi Zosen Corp Column welding equipment in structures

Also Published As

Publication number Publication date
DE2967045D1 (en) 1984-07-12
EP0018445A1 (en) 1980-11-12
EP0018445B1 (en) 1984-06-06
EP0018445B2 (en) 1990-01-03
DE2853870C2 (en) 1987-08-06
DE2853870A1 (en) 1980-07-03
ZA796750B (en) 1980-11-26
JPS5594459A (en) 1980-07-17

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