JPS6026610A - Production of cv graphite cast iron - Google Patents

Production of cv graphite cast iron

Info

Publication number
JPS6026610A
JPS6026610A JP58134354A JP13435483A JPS6026610A JP S6026610 A JPS6026610 A JP S6026610A JP 58134354 A JP58134354 A JP 58134354A JP 13435483 A JP13435483 A JP 13435483A JP S6026610 A JPS6026610 A JP S6026610A
Authority
JP
Japan
Prior art keywords
cast iron
molten metal
graphite cast
low
graphite
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.)
Granted
Application number
JP58134354A
Other languages
Japanese (ja)
Other versions
JPH0357164B2 (en
Inventor
Tomoji Ashikawa
芦川 友治
Takeshi Mitsuya
三ツ矢 彪
Tatsuo Suzuki
達夫 鈴木
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.)
MEIDEN CHUKO KK
Meidensha Corp
Meidensha Electric Manufacturing Co Ltd
Original Assignee
MEIDEN CHUKO KK
Meidensha Corp
Meidensha Electric Manufacturing Co Ltd
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 MEIDEN CHUKO KK, Meidensha Corp, Meidensha Electric Manufacturing Co Ltd filed Critical MEIDEN CHUKO KK
Priority to JP58134354A priority Critical patent/JPS6026610A/en
Publication of JPS6026610A publication Critical patent/JPS6026610A/en
Publication of JPH0357164B2 publication Critical patent/JPH0357164B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21CPROCESSING OF PIG-IRON, e.g. REFINING, MANUFACTURE OF WROUGHT-IRON OR STEEL; TREATMENT IN MOLTEN STATE OF FERROUS ALLOYS
    • C21C1/00Refining of pig-iron; Cast iron
    • C21C1/10Making spheroidal graphite cast-iron
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P10/00Technologies related to metal processing
    • Y02P10/20Recycling

Abstract

PURPOSE:To obtain efficiently a CV graphite cast iron having excellent mechanical characteristics by adding a CV treating alloy consisting of Fe-Mg-Ca-Ce alloy to a molten base metal having a prescribed compsn., subjecting the same to a pocket process treatment, inoculating Fe-Si and casting the molten metal. CONSTITUTION:Silicon steel plate scrap, low-S carburized material and Fe-Si are melted in the remaining molten metal corresponding to FC15 and the molten metal is then desulfurized by using a low frequency induction furance, by which the molten base metal for a spheroidal graphite cast iron consisting of 3.6- 3.9wt% T.C, 1.4-1.6% Si, 0.3-0.4% Mn, 0.044-0.057% P, 0.02-0.03% S and the balance Fe is produced. A CV treating alloy consisting of 1.5Mg-0.4%Ca-3.5%Ce- the balance Fe is added at 1.04-1.15% to the molten base metal which is then subjected to a pocket process treatment. The molten metal is thereafter inoculated by Fe-Si and is cast. The CV graphite cast iron having excellent characteristics such as tensile strength, elongation, hardness, etc. is stably obtd. by the above-mentioned method.

Description

【発明の詳細な説明】 本発明はコンパクテド・バーミキュラー黒鉛鋳鉄(以下
C,V、黒鉛鋳鉄という)の製造方法、詳しくは低周波
誘導炉溶解の脱硫処理された溶湯組成、溶湯温度、処理
量の変動の小さい球状黒鉛鋳鉄用溶湯を用いて、Fe 
−Mg Ca Ce 系合金処理により安定してCVV
鉛鋳鉄を製造する方法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing compacted vermicular graphite cast iron (hereinafter referred to as C, V, graphite cast iron). Using molten metal for spheroidal graphite cast iron with small fluctuation, Fe
- Stable CVV by Mg Ca Ce alloy treatment
The present invention relates to a method for manufacturing lead cast iron.

要とする。Mgでの球状化処理溶湯が鋳型に注湯されず
保持されると、時間とともにMgは溶湯から逸出し所謂
フエイデイング現象を起し、残留Mg量は急減する。溶
湯の保持時間が長(なると、黒鉛は球状化しな(なる。
Essential. Spheroidization treatment with Mg If the molten metal is held without being poured into a mold, Mg escapes from the molten metal over time, causing a so-called fading phenomenon, and the amount of residual Mg rapidly decreases. If the molten metal is held for a long time, the graphite will not become spheroidized.

しかし微量のMgの影響で、先端が丸味をもった、いも
去状の黒鉛が現れる。この鋳鉄をコンパクテド・バーミ
キュラ黒鉛鋳鉄(C,V、黒鉛鋳鉄)と呼んでいる。こ
のC,V、黒鉛鋳鉄鉱、引張強さや伸びの点で球状黒鉛
鋳鉄に劣るが、片状黒鉛鋳鉄よりもずっとよ(、振動減
衰能、熱伝導度などの点で片状黒鉛鋳鉄に劣るが球状黒
鉛鋳鉄よりも優れているものである。
However, due to the influence of a small amount of Mg, graphite with a rounded tip appears. This cast iron is called compacted vermicular graphite cast iron (C, V, graphite cast iron). This C, V, graphite cast iron ore is inferior to spheroidal graphite cast iron in terms of tensile strength and elongation, but is much better than flake graphite cast iron (inferior to flake graphite cast iron in terms of vibration damping ability, thermal conductivity, etc.) is superior to spheroidal graphite cast iron.

従来CV黒鉛鋳鉄をMg −Ca −Ce系合金の添加
処理によって現場的に製造するときは、冗漫中のS含有
量を正確に知ることが難しいこと、添加方法が単なる置
注ぎ法による添加合金の有効性が劣化し、過剰添加によ
る不経済等なかなかCV黒鉛鋳鉄製造のための適正添加
量の把握が困難でめったことが実情である。
Conventionally, when CV graphite cast iron is produced on-site by addition treatment of Mg-Ca-Ce alloy, it is difficult to know the S content in the redundant accurately, and the addition method is a simple pouring method. The reality is that it is difficult to determine the appropriate amount of addition for CV graphite cast iron production, resulting in decreased effectiveness and uneconomical effects due to excessive addition.

本発明はMg −Ca −Ce 鉄系合金を添加処理し
、CV黒鉛鋳鉄を製造するに当って、従来の上述の問題
点を解消し機械的特性値においても優れたCV黒鉛鋳鉄
を能率良く製造する方法を提供すること全目的とするも
のである。
The present invention solves the above-mentioned conventional problems in manufacturing CV graphite cast iron by adding Mg-Ca-Ce iron-based alloy, and efficiently manufactures CV graphite cast iron with excellent mechanical properties. The overall purpose is to provide a method for doing so.

本発明の要旨は低周波誘導炉を用いて、該炉のFC15
相当の残湯に、けい素鋼板層、低Sの加炭材、Fe−8
i を装入溶解し、得られた溶湯に脱硫剤を添加し、T
、C:3.6〜3.9mJt%、Si:1.4る球状黒
鉛銑鉄用溶湯の冗漫を溶製し、該冗漫にポケット法処理
を行いF’e−8tで接種し鋳込むことを特徴とするC
V黒鉛鋳鉄の製造方法にある。
The gist of the present invention is to use a low frequency induction furnace to
A considerable amount of residual hot metal, silicon steel plate layer, low S recarburizer, Fe-8
i is charged and melted, a desulfurizing agent is added to the obtained molten metal, and T
, C: 3.6 to 3.9 mJt%, Si: 1.4, a molten metal for spheroidal graphite pig iron is melted, and the molten metal is subjected to pocket method treatment, inoculated with F'e-8t, and cast. Characteristic C
It is in the manufacturing method of V-graphite cast iron.

以下本発明の詳細について、実施例の知見に基づいて述
べる。
The details of the present invention will be described below based on the findings of Examples.

本発明は低周波誘導炉を用いること全特徴とし、該炉の
FC−i5相当の残湯に、けい素鋼板層。
The present invention is characterized in that a low frequency induction furnace is used, and the remaining molten metal equivalent to FC-i5 in the furnace is coated with a silicon steel sheet layer.

故銑、低S加炭材として電極黒鉛層、Fe−8i を適
宜配合して溶解し、取鍋に出湯温度1520土10℃に
て移しとって低S溶湯をうるために脱硫処理を行なう。
The waste pig iron, an electrode graphite layer as a low S recarburizing material, and Fe-8i are suitably blended and melted, and the mixture is transferred to a ladle at a tapping temperature of 1520° C. and desulfurized to obtain a low S molten metal.

Stをき有する溶湯中にては脱硫できないので、取鍋や
キュポラの前炉などで脱硫剤としてソーダ灰9石灰、カ
ルシウムカーバイド等を用いて脱硫する。カルシウムカ
ーバイドCαCが脱硫率の点で好ましくその添加量は溶
湯に対して0.5%であり、処理温度が高い程脱硫反応
が速く進むので前記出湯温度の範囲が好ましい。
Since desulfurization cannot be performed in a molten metal containing St, desulfurization is carried out in a ladle or cupola forehearth using soda ash 9 lime, calcium carbide, or the like as a desulfurization agent. Calcium carbide CαC is preferable from the viewpoint of desulfurization rate, and its addition amount is 0.5% based on the molten metal, and the desulfurization reaction proceeds more quickly as the treatment temperature is higher, so the above range of tapping temperature is preferable.

斯くしてT、C:3,6〜6.9%、Si:1.4〜1
.6%、 Mn: [1,3〜0.4%、p : 0.
044〜O,[357%。
Thus T, C: 3.6-6.9%, Si: 1.4-1
.. 6%, Mn: [1.3-0.4%, p: 0.
044~O, [357%.

S:0.02〜0.06%残部Feからなる組成範囲に
なるよう冗漫を溶製する。本発明者はこの冗漫に対して
1.5%Mg −0,4%ca−3,5%Ce残部Fe
の合金をCV化処理合金として添加量を種々変化せしめ
、Fe−81(Sj : 50%)を黒鉛の粒数調整、
チル化の防IFやパーライト地金フェライト地にするた
め0.5%添加接種し、1680〜1480℃で鋳込ん
で組織を顕微鏡で観察しCV化をしらべた。この場合0
69%添加でlハ添加合金を単に取鍋底に設置し溶湯を
注ぐ置注ぎ法と取鍋底に一部ポケット部を構築してその
中に添加合金を設置し溶湯を注ぐポケット法のいずれに
おいても参考写真トI[11に示すようにCV黒鉛鋳鉄
は得られなかった。
S: The redundant is melted to have a composition range of 0.02 to 0.06% with the balance being Fe. The present inventor has solved this redundancy with 1.5% Mg - 0.4% ca - 3.5% Ce and balance Fe
The alloy was used as a CV treated alloy and the amount added was varied, Fe-81 (Sj: 50%) was adjusted to the number of graphite grains,
In order to prevent IF from chilling and to create a pearlite base ferrite base, 0.5% inoculation was added, cast at 1680-1480°C, and the structure was observed under a microscope to check for CV conversion. In this case 0
Both the pouring method where the 69% additive alloy is simply placed on the bottom of the ladle and pouring the molten metal, and the pocket method where a pocket is constructed at the bottom of the ladle, the additive alloy is placed in it, and the molten metal is poured. As shown in reference photograph I [11], no CV graphite cast iron was obtained.

つぎに1,1%象加で、ポケット法による場合は写真阻
2に示す如<CV黒鉛鋳鉄は得られたが置注ぎ法による
場合は写真Nn3に示す如くcv黒鉛鋳鉄は得られなか
った。さらに1.2%添加では写真IVkL4に示す如
(置注ぎ法ポケット法いずれにおいても、CV黒鉛組織
が認められるが同時に球状黒鉛が多く出現し、さらに基
地に遊離セメントが出現し好ましくなかった。
Next, with 1.1% inlay, when using the pocket method, CV graphite cast iron was obtained as shown in Photo No. 2, but when using the pouring method, no CV graphite cast iron was obtained as shown in Photo No. 3. Furthermore, when adding 1.2%, as shown in Photo IVkL4 (in both the pouring method and the pocket method, a CV graphite structure was observed, but at the same time, a large amount of spheroidal graphite appeared, and furthermore, free cement appeared in the matrix, which was not desirable).

以上より添加量1.1%前後かCV黒鉛鋳鉄製造に好ま
しいことが判明したので、さらに11%前後でポケット
法添加の実験を重ねた結果、1,04〜1.15重量%
の範囲内で引張り強さ34〜404g//胴2.伸び4
.2〜7.0%、硬さHB 160〜180の優れたC
V黒鉛鋳鉄が経済的に安定して得られた。
From the above, it was found that an addition amount of around 1.1% is preferable for CV graphite cast iron production, and as a result of repeated experiments with the pocket method addition at around 11%, the result was 1.04 to 1.15% by weight.
Tensile strength within the range of 34 to 404 g //Channel 2. Elongation 4
.. Excellent C of 2-7.0%, hardness HB 160-180
V-graphite cast iron was economically and stably obtained.

以下実施例について述べる。Examples will be described below.

実施例1 6トン容量低周波誘導炉を用いて、FC15相当の残湯
、けい素鋼板層、故銑、′電極黒鉛屑の低S加炭材、F
e−8i(St : 50%)合金を適宜配合して溶解
し、出湯温度1520±10′Cにて、取鍋に移しとっ
た500〜600kgの溶湯に、脱硫剤としてC60’
c 0.5%を添加して脱硫した球状黒鉛鋳鉄用溶湯の
冗漫を溶製する。この場合冗漫の組成は次の範囲になる
よう制御する。
Example 1 Using a 6-ton capacity low-frequency induction furnace, residual metal equivalent to FC15, silicon steel plate layer, waste pig iron, low S carburization material of 'electrode graphite scrap, F
E-8i (St: 50%) alloy was suitably mixed and melted, and C60' was added as a desulfurizing agent to 500 to 600 kg of molten metal, which was transferred to a ladle at a tapping temperature of 1520±10'C.
c. Add 0.5% of desulfurized molten metal for spheroidal graphite cast iron. In this case, the redundant composition is controlled to be within the following range.

T、 C,二 3. 6 〜3. 9 %、 Si :
 1. 4 〜1. 6 %、 Mn二0.6〜0.4
%、p : 0.044〜0.057%、 S。
T, C, two 3. 6-3. 9%, Si:
1. 4 ~1. 6%, Mn2 0.6-0.4
%, p: 0.044-0.057%, S.

0.02〜0.03% 残部Fe 上上記揚湯対して、1.5%Mg O,4%Ca−6,
5%Ce−残部Fe の合金′!1l−0,9,1,1
,1,2%添加し、Fe−8t(St :50%)合金
0.5%で接1重し1680゜〜1480℃で鋳込む。
0.02-0.03% Balance Fe For the above fried hot water, 1.5% Mg O, 4% Ca-6,
5% Ce-balance Fe alloy'! 1l-0,9,1,1
, 1.2%, and 0.5% of Fe-8t (St: 50%) alloy is added at 1 weight and cast at 1680° to 1480°C.

合金添加に当って置注ぎ法とポケット法の2種について
行い、得られた黒鉛鋳鉄の組織を顕微鏡にて200倍に
拡大し、1睨察した組織の状態を参考写真Nll−1東
4に示す。
Two methods were used to add the alloy: the pouring method and the pocket method.The structure of the graphite cast iron obtained was magnified 200 times with a microscope, and the state of the structure observed at one glance is shown in reference photo Nll-1 East 4. show.

写真陽1は前述球状黒鉛鋳鉄用溶湯の冗漫に対して、F
e −Mg−Ca−Ce @金ヲ0.9%、置注ぎ法筐
たはポケット法によって処理し、Fe−8i(St :
50%)0.5%で接種しfc場合の鋳鉄組織でCV黒
鉛が認められず本添加量ではCVV鉛鋳鉄は得られない
Photo 1 shows F
Fe-8i (St:
50%) CV graphite is not observed in the cast iron structure when fc is inoculated at 0.5%, and CVV lead cast iron cannot be obtained with this addition amount.

写真N112 iは、前記の冗漫に対して、同じ(Fe
−Mg −Ca−Ce合金11%ポケット法によって処
理し、Fe−8i(St : 50%)0.5%で接種
した場合の7.tノ!鉄組織でCV黒黒鉛低紙認められ
CVV鉛鋳鉄である。機械的性質は引張り強さ36 ’
 f’、f /Wnn2H伸び4.2%ブリネル硬さ値
は16ろであった。
Photograph N112i has the same (Fe
-Mg-Ca-Ce alloy 11% treated by pocket method and inoculated with 0.5% Fe-8i (St: 50%) 7. T-no! The iron structure is CVV lead cast iron with low CV graphite. Mechanical properties are tensile strength 36'
f', f /Wnn2H elongation 4.2% Brinell hardness value was 16 F.

写真N[lL3は、前記合金11%を市注ぎ法によって
処理し、同様々接錘全行つ/こ〜合の鍜j鉄組織でCV
黒鉛組絨が認められなかった。この粗大片状黒鉛鋳鉄は
写j’4Nn1とほぼ同様であり引張り強さ12〜16
 ’gf/mm2T <申ひ0%、ブリネルもり、1.
−、X値は126〜167であった。
Photo N [lL3 shows the CV of the alloy 11% processed by the market pouring method and the iron structure of this case.
No graphite carpet was observed. This coarse flaky graphite cast iron is almost the same as photoj'4Nn1 and has a tensile strength of 12 to 16.
'gf/mm2T <0%, Brinell, 1.
-, X values were 126-167.

写真Nu Aは、前記合金12%を直圧ぎ法7[たはポ
ケット法によって処理し、同様な接イ!]!を行った場
合の鋳鉄低域で、CV愚鉛組低域同時に球状黒鉛が多(
、かつ基地Vこ遊離した七メンタイトも認められ、引張
強さ52.6ルgf/□2.伸び2″;b、ブリネル硬
さ値は212であり、CVV鉛鋳鉄と1゜では好捷しい
ものではなかつ/こ。
Photo Nu A shows that 12% of the above alloy was processed by the direct pressure method 7 [or the pocket method] and the same bonding method was applied. ]! In the cast iron low range when doing this, there is a lot of spheroidal graphite (
, and free heptite was also observed, and the tensile strength was 52.6 gf/□2. The elongation is 2''; b, and the Brinell hardness value is 212, which is not favorable at 1° with CVV lead cast iron.

実施例2 実施例1と同様に冗漫を得て、この冗漫に対しCV化処
理全実施例10合金添加tを11%前後でかつポケット
法による添加により処理し得られたCVV鉛鋳鉄の物理
性を調べた、その結果添加fr1.04〜1.15%の
範囲で引張り強さ6A〜dOAg//咽”)伸び4.2
〜7.0%、 硬さHB 160〜180の特性値が得
られた。
Example 2 Physical properties of CVV lead cast iron obtained by obtaining redundancy in the same manner as in Example 1 and treating this redundancy with CV treatment All Examples 10 alloy addition t was around 11% and addition by pocket method As a result, the tensile strength ranged from 6 A to dOAg//Elongation 4.2 within the range of addition fr 1.04 to 1.15%.
Characteristic values of hardness HB 160-180 were obtained.

代理人 弁理士 木 村 三 朗Agent: Patent Attorney Sanro Kimura

Claims (2)

【特許請求の範囲】[Claims] (1)低周波誘導炉を用いて、該炉のFC15相当の残
湯に、けい素鋼板層、低Sの加炭材、Fe−81を装入
溶解し、得られた溶湯に脱硫剤を添加し、鉄用浴湯の冗
漫を溶製し、該冗漫に対して1.5%処理を行いF e
 −84で接種し、鋳込むことを特徴とするCVV鉛鋳
鉄の製造方法。
(1) Using a low-frequency induction furnace, charge and melt a silicon steel sheet layer, low S recarburizer, and Fe-81 into the remaining molten metal equivalent to FC15 in the furnace, and add a desulfurization agent to the resulting molten metal. Addition of Fe
A method for producing CVV lead cast iron, which comprises inoculating with -84 and casting.
(2)前記球状黒鉛鋳鉄用溶湯の冗漫を溶製するに当り
、故銑ならび圧低S加炭材として電極黒鉛前記組成の冗
漫を溶製し、該冗漫に前記CV処処理台ことを特徴とす
る特許請求の範囲第1項記載のCVV鉛鋳鉄の製造方法
(2) In melting the redundant molten metal for spheroidal graphite cast iron, the redundant iron and the electrode graphite having the above composition are melted as a low-pressure S carburizing material, and the redundant is used in the CV treatment table. A method for manufacturing CVV lead cast iron according to claim 1.
JP58134354A 1983-07-25 1983-07-25 Production of cv graphite cast iron Granted JPS6026610A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP58134354A JPS6026610A (en) 1983-07-25 1983-07-25 Production of cv graphite cast iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP58134354A JPS6026610A (en) 1983-07-25 1983-07-25 Production of cv graphite cast iron

Publications (2)

Publication Number Publication Date
JPS6026610A true JPS6026610A (en) 1985-02-09
JPH0357164B2 JPH0357164B2 (en) 1991-08-30

Family

ID=15126402

Family Applications (1)

Application Number Title Priority Date Filing Date
JP58134354A Granted JPS6026610A (en) 1983-07-25 1983-07-25 Production of cv graphite cast iron

Country Status (1)

Country Link
JP (1) JPS6026610A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002146468A (en) * 2000-11-02 2002-05-22 Kitagawa Iron Works Co Ltd Cast iron having high vibration damping capacity and its production method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5361513A (en) * 1976-11-16 1978-06-02 Osaka Tokushiyu Goukin Kk Addition alloy for making semiductile cast iron
JPS5616613A (en) * 1979-07-21 1981-02-17 Toyota Motor Corp Additive for cast iron
JPS5693808A (en) * 1979-12-19 1981-07-29 Foseco Int Molten metal treating agent and production of vermicular graphite cast iron

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5361513A (en) * 1976-11-16 1978-06-02 Osaka Tokushiyu Goukin Kk Addition alloy for making semiductile cast iron
JPS5616613A (en) * 1979-07-21 1981-02-17 Toyota Motor Corp Additive for cast iron
JPS5693808A (en) * 1979-12-19 1981-07-29 Foseco Int Molten metal treating agent and production of vermicular graphite cast iron

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002146468A (en) * 2000-11-02 2002-05-22 Kitagawa Iron Works Co Ltd Cast iron having high vibration damping capacity and its production method

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JPH0357164B2 (en) 1991-08-30

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