[go: up one dir, main page]

JPS62256913A - Manufacture of high strength black heat malleable cast iron - Google Patents

Manufacture of high strength black heat malleable cast iron

Info

Publication number
JPS62256913A
JPS62256913A JP9992486A JP9992486A JPS62256913A JP S62256913 A JPS62256913 A JP S62256913A JP 9992486 A JP9992486 A JP 9992486A JP 9992486 A JP9992486 A JP 9992486A JP S62256913 A JPS62256913 A JP S62256913A
Authority
JP
Japan
Prior art keywords
cast iron
malleable cast
pig iron
high strength
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.)
Pending
Application number
JP9992486A
Other languages
Japanese (ja)
Inventor
Shinya Mizuno
慎也 水野
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 JP9992486A priority Critical patent/JPS62256913A/en
Publication of JPS62256913A publication Critical patent/JPS62256913A/en
Pending legal-status Critical Current

Links

Landscapes

  • Heat Treatment Of Steel (AREA)
  • Heat Treatment Of Articles (AREA)

Abstract

PURPOSE:To manufacture high strength black heat malleable cast iron by chilling the surface of white pig iron and subjecting the pig iron to austenitizing, rapid cooling and isothermal transformation under specified conditions so as to make the structure fine. CONSTITUTION:A part or the whole of the surface layer of white pig iron is melted by rapid heating and is rapidly cooled to form a chilled structure. The pig iron is then held at 870-1,050 deg.C for >=30min to carry out graphitizing as well as austenitizing and it is rapidly cooled to 200-400 deg.C and is held at the temp. for >=10min to convert the structure of the matrix into bainite by isothermal transformation. By this method, high strength black heart malleable cast iron having a fine structure can be manufactured in a short time.

Description

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

〔産業上の利用分野〕 本発明は高強度黒心可鍛鋳鉄の製造方法に関するもので
ある。 〔従来の技術〕 従来、高強度材料として鍛鋼が用いられているが、鍛造
は鋳造に比べて製造コストが高く、また、複雑な形状の
製品を作るのが困難である。 そこで、複雑な形状でも容易に安価に製造できる鋳鉄の
高強度化が行われている。 上記の鋳鉄の高強度化としては、例えば白銑に第一、第
二段にわたる黒鉛死焼なましを施して悪心可鍛鋳鉄とす
る方法が行われている。また、最近、高強度化するため
に、白銑を950℃の塩浴中で4ないし8時間保持して
オーステナイト化し、250ないし450°Cの塩浴中
で1時間保持してオーステンパー処理して基地をベーナ
イト組織にする可鍛鋳鉄のオーステンパー処理が提案さ
れている(内山ら、日不鋳物協会第106 回全国講演
大会講演概要集16頁)。 〔発明が解決しようとする問題点〕 しかしながら、上記悪心可鍛鋳鉄は、鋳放しでも表面が
チル化するが、チル組織が荒いため、黒鉛化処理におい
て析出する黒鉛が大きく、強度は十分ではない。また、
オーステンパー処理を施した可鍛鋳鉄は、上記と同様に
、通常の白銑ではチル組織が荒いため、その後の黒鉛化
処理において析出する黒鉛が大きく、またオーステンパ
ー処理によってできるベイナイト組織も荒くなり、強度
は十分高いとは言えない。 本発明は上記問題点を解決するためのもので、高強度の
焦心可鍛鋳鉄の製造方法を提供することを目的とするも
のである。 〔問題点を解決するための手段〕 本発明の高強度焦心可鍛鋳鉄は、白銑の表面層の一部又
は全部を急速加熱して溶融し、急冷することによりチル
化したのち、該白銑を870ないし1050℃で30分
間以上保持してオーステナイト化処理し、その後急冷し
、200 ないし400°Cで10分間以上保持して恒
温変態処理することを特徴とするものである。 表面層のみを゛急速に加温して溶融する方法としては、
高密度にエネルギーを与えることができるティグアーク
(tungsten −1nert −gas arc
 )、プラズマジェットトーチ、レーザーなどを短時間
当てる方法が挙げられる。 本発明に用いる白銑は、析出する黒鉛を球状にするため
にマグネシウム(Mg )  を添加してもよい。 〔作 用〕 白銑の表面層の一部又は全部を急速に加熱して溶融し、
急冷することによジチル化するため、表面層の一部又は
全部が細かいチル組織となる。 このチル化した白銑を870ないし1050°Cで30
分以上保持することにより細かいチル組織中のセメンタ
イトが細かい黒鉛となるとともに基地がオーステナイト
化する。次いで急冷して20Gないし400℃で10分
間以上保持して恒温変態処理することによυ基地が細か
いベイナイト組織となる。 以下に限定理由を述べる。 オーステナイト化処理は、基地をオーステナイト化する
と同時にセメンタイトを黒鉛化するためのもので、87
0℃未満の温度では黒鉛化が著しく遅くなり、1050
℃を越えるとオーステナイト粒及び黒鉛が粗大化するた
め、処理温度は870ないし1050 ”(lとした。 また、処理時間は、30分未満では十分に黒鉛化しない
ため、50分以上とした。 恒温変態処理は基地のオーステナイトをベイナイト化す
るためのもので、処理温度は200℃未満では基地がぜ
い化し、400℃ を越るとベイナイト組織が荒くなり
、強度が低下するため、200ないし400℃とした。 処理時間は10分未満では十分ベイナイト化することが
できず、もろくなるため、10分以上とした。 〔実施例〕 本発明を一実施例により説明する。 実施例1 炭素(C)2%、ケイ素(Si)t3チ、マンガン(M
n)α3チ、リン(P)IllL01%、硫黄(S)α
08%及び残部鉄(Fe)からなる白銑の表面を、ティ
グ(TIG)  を走査して表面から2n程度の深さま
で溶融した。ティグは走査しているため、溶融した部分
は他の加熱されていない部分へ放熱して急冷され、チル
化し、表面層は細かいチル組織となる。次に、900”
(l で2時間保持してオーステナイト化するとともに
黒鉛化した。次いで急冷して575℃クシ、その温度で
1時間保持して恒温変態処理を行って基地をベイナイト
化し九〇 比較例1として、実施例1で用いたのと同成分の白銑を
用いて、ティグ処理せずに、実施例1と同一条件で、オ
ーステナイト化処理及び恒温変態処理からなるオーステ
ンパー処理を施した。 実施例1及び比較例1の焦心可鍛鋳鉄の表面層の金属組
織を表わす顕微鏡写真をそれぞれ第1図及び第2図に示
す。実施例1は比較例1に比べて黒鉛及びベイナイト組
織が微細であった。 これはチル化によりチル組織が細かくなったためである
。また、チル組織が細かいため比較的短時間で黒鉛化す
ることができた。 表1に両者の引張り強さ及び疲れ限度を示す。 なお、疲れ限度は小野式回転曲げ疲労試験によシ平滑試
験片を用いて求めた。 表1 引張り強さ及び疲れ限度は、比較例1がそれぞれ824
f/in、 35 Qf/dであるのに対し、実施例1
はそれぞれ102即f/ld、43即f/xiと大きく
、強度が優れている。これは実施例1の金属組織が微細
なためである。 実施例2 実施例1で用いた白銑と同成分のものを用い、白銑の表
面を実施例1と同一条件でティグ処理してチル化した。 次
[Industrial Field of Application] The present invention relates to a method for manufacturing high-strength black-core malleable cast iron. [Prior Art] Conventionally, forged steel has been used as a high-strength material, but forging has higher manufacturing costs than casting, and it is difficult to manufacture products with complex shapes. Therefore, efforts are being made to improve the strength of cast iron, which can be manufactured easily and inexpensively even in complex shapes. In order to increase the strength of cast iron, for example, white pig iron is subjected to first and second stages of graphite dead annealing to obtain core malleable cast iron. Recently, in order to increase the strength, white pig iron is austenitized by holding it in a salt bath at 950°C for 4 to 8 hours, and austempering by holding it in a salt bath at 250 to 450°C for 1 hour. Austempering treatment of malleable cast iron to make the base into a bainite structure has been proposed (Uchiyama et al., Japan-Foundry Association 106th National Lecture Conference Abstracts, p. 16). [Problems to be Solved by the Invention] However, the surface of the above-mentioned core malleable cast iron is chilled even when it is as cast, but because the chill structure is rough, a large amount of graphite precipitates during graphitization treatment, and the strength is not sufficient. . Also,
As mentioned above, in malleable cast iron that has been subjected to austempering treatment, the chill structure of ordinary white pig iron is rough, so the graphite that precipitates in the subsequent graphitization treatment is large, and the bainite structure formed by austempering treatment is also rough. , the strength cannot be said to be sufficiently high. The present invention is intended to solve the above-mentioned problems, and an object of the present invention is to provide a method for manufacturing high-strength focused malleable cast iron. [Means for Solving the Problems] The high-strength focused malleable cast iron of the present invention rapidly heats part or all of the surface layer of white pig iron to melt it, chills it by rapid cooling, and then melts the surface layer of the white pig iron. It is characterized by holding the pig iron at 870 to 1050°C for 30 minutes or more to austenitize it, then rapidly cooling it, and holding it at 200 to 400°C for 10 minutes or more to perform isothermal transformation treatment. A method of rapidly heating and melting only the surface layer is as follows:
Tungsten gas arc can provide energy at high density.
), plasma jet torch, laser, etc. for a short period of time. Magnesium (Mg) may be added to the white pig iron used in the present invention in order to make the precipitated graphite spherical. [Function] Rapidly heats and melts part or all of the surface layer of white pig iron,
Since dithylation occurs by rapid cooling, part or all of the surface layer becomes a fine chilled structure. This chilled white pig iron is heated at 870 to 1050°C for 30 minutes.
By holding the temperature for more than a minute, the cementite in the fine chilled structure becomes fine graphite and the base becomes austenite. Next, it is rapidly cooled and held at 20G to 400°C for 10 minutes or more to perform isothermal transformation treatment, so that the υ base becomes a fine bainite structure. The reasons for this limitation are explained below. The austenitization process is to austenite the base and graphitize the cementite at the same time.
At temperatures below 0°C, graphitization is significantly slowed down and 1050
If the temperature exceeds ℃, the austenite grains and graphite will become coarse, so the treatment temperature was set to 870 to 1050'' (l).The treatment time was set to 50 minutes or more, since graphitization would not be sufficient if it was less than 30 minutes. Transformation treatment is to convert austenite in the matrix into bainite. If the treatment temperature is less than 200°C, the matrix becomes brittle, and if it exceeds 400°C, the bainite structure becomes rough and the strength decreases, so the treatment temperature is 200 to 400°C. If the treatment time is less than 10 minutes, sufficient bainite formation cannot be achieved and the material becomes brittle, so the treatment time was set to 10 minutes or more. [Example] The present invention will be explained by an example. Example 1 Carbon (C) 2%, silicon (Si) t3, manganese (M
n) α3, phosphorus (P) IllL01%, sulfur (S) α
The surface of white pig iron consisting of 0.8% iron (Fe) and the balance was melted to a depth of about 2n from the surface by scanning with a TIG. Since the TIG scans, the melted part radiates heat to other unheated parts and is rapidly cooled, becoming chilled, and the surface layer becomes a fine chilled structure. Next, 900”
(l) for 2 hours to austenitize and graphitize. Next, it was rapidly cooled to 575℃, and kept at that temperature for 1 hour to perform isothermal transformation treatment to convert the base to bainite. Using white pig iron with the same composition as that used in Example 1, an austempering treatment consisting of an austenitization treatment and a constant temperature transformation treatment was performed under the same conditions as in Example 1 without TIG treatment.Example 1 and Micrographs showing the metal structure of the surface layer of the focused malleable cast iron of Comparative Example 1 are shown in FIGS. 1 and 2, respectively. In Example 1, the graphite and bainite structures were finer than in Comparative Example 1. This is because the chilled structure became finer due to chilling.Also, because the chilled structure was finer, it was possible to graphitize in a relatively short time.Table 1 shows the tensile strength and fatigue limit of both. The fatigue limit was determined by the Ono rotary bending fatigue test using a smooth test piece. Table 1 Tensile strength and fatigue limit were 824 for Comparative Example 1, respectively.
f/in, 35 Qf/d, whereas in Example 1
are as large as 102 f/ld and 43 f/xi, respectively, and have excellent strength. This is because the metal structure of Example 1 is fine. Example 2 Using white pig iron having the same composition as that used in Example 1, the surface of the white pig pig was subjected to TIG treatment under the same conditions as in Example 1 to chill it. Next

【、実施例1と同一条件でオーステナイト化し、急冷
して230℃にし、その温度で2時間保持して恒温変態
処理することによりオーステンパー旭】を施した。 比較例2として、実施例2と同成分の白銑を用いて、テ
ィグ処理はせずに、実施例2と同一条件でオーステンパ
ー処理を施した。 実施例2及び比較例20黒心可態鋳鉄の表面層の金属組
織を表わす顕微鏡写真をそれぞれ第3図及び第4図に示
す。実施例2は比較例2に比べて黒鉛及びベイナイト組
織が微細であった。 これはチル化によりチル組織が細かくなったためである
。また、チル組織が細かいため比較的短時間で黒鉛化す
ることができた。 表2に実施例2及び比較例2の引張り強さ及び疲れ限度
を示す。なお、疲れ限度は小野式回転曲げ疲労試験によ
り平滑試験片を用いて求めた。 表2 引張シ強さ及び疲れ限度は、比較例2がそれぞれ98即
f/Id、  32即f/dであるのに対して、実施例
2はそれぞれ152即レー、40 QiAIIと大きく
、優れている。これは実施例2の金属組織が微細なため
である。 〔発明の効果〕 本発明の製造方法は、上記したように、白銑を再チル化
してチル組織を微細にしたのち、オースチッパ処理する
ので、黒鉛及びベイナイト組織が微細になυ、高強度の
悪心可鍛鋳鉄を製造することができる。更にまた、チル
組織が微細なため、比較的短時間で黒鉛化することがで
きる。そのため、製造コストの低減が可能である。 更に、本発明の方法によυ製造した悪心可鍛鋳鉄は高強
度であるため、鍛鋼の代替として用いることにより低コ
スト化、軽量化が図れるとともに、複雑な形状でも高強
度の製品を容易に製造することができる。
[Austenitization was performed under the same conditions as in Example 1, rapidly cooled to 230° C., and maintained at that temperature for 2 hours to carry out a constant temperature transformation treatment to perform austempering]. As Comparative Example 2, austempering treatment was performed under the same conditions as Example 2 using white pig iron having the same composition as in Example 2 without TIG treatment. Microscopic photographs showing the metallographic structure of the surface layer of the black-core malleable cast iron of Example 2 and Comparative Example 20 are shown in FIGS. 3 and 4, respectively. In Example 2, the graphite and bainite structures were finer than in Comparative Example 2. This is because the chilled structure became finer due to chilling. In addition, since the chill structure was fine, graphitization could be achieved in a relatively short time. Table 2 shows the tensile strength and fatigue limit of Example 2 and Comparative Example 2. The fatigue limit was determined by the Ono rotary bending fatigue test using a smooth specimen. Table 2 The tensile strength and fatigue limit of Comparative Example 2 are 98 instant f/Id and 32 instant f/d, respectively, whereas Example 2 has a large and excellent tensile strength of 152 instant f/Id and 40 QiAII, respectively. There is. This is because the metal structure of Example 2 is fine. [Effects of the Invention] As described above, in the manufacturing method of the present invention, the white pig iron is re-chilled to make the chill structure fine and then subjected to auschipper treatment, so that the graphite and bainite structures become fine υ, resulting in high strength. Nausea malleable cast iron can be manufactured. Furthermore, since the chill structure is fine, it can be graphitized in a relatively short time. Therefore, manufacturing costs can be reduced. Furthermore, since the core malleable cast iron manufactured by the method of the present invention has high strength, it can be used as a substitute for forged steel to reduce costs and weight, and it is also possible to easily manufacture high-strength products even with complex shapes. can be manufactured.

【図面の簡単な説明】[Brief explanation of drawings]

第1図は本発明の実施例1で製造した悪心可鍛鋳鉄の表
面層の金属組織の顕微鏡写真、第2図は比較例1で製造
した悪心可鍛鋳鉄の表面層の金属組織の顕微鏡写真、 第5図は本発明の実施例2で製造した悪心可鍛鋳鉄の表
面層の金属組織の顕微鏡写真、第4図は比較例2で人造
した悪心可鍛鋳鉄の表面層の金属組織の顕微鏡写真を表
わす。 特許出願人  トヨタ自動車株式会社 第1114 第3!ヅ (100侶) ・ρ、2 :′、 (1001音) 伐 4  ′ (100格)
Figure 1 is a micrograph of the metal structure of the surface layer of the core malleable cast iron produced in Example 1 of the present invention, and Figure 2 is a micrograph of the metal structure of the surface layer of the core malleable cast iron produced in Comparative Example 1. , Figure 5 is a microscopic photograph of the metal structure of the surface layer of the core malleable cast iron manufactured in Example 2 of the present invention, and Figure 4 is a microscope photo of the metal structure of the surface layer of the core malleable cast iron manufactured in Comparative Example 2. Represents a photo. Patent applicant Toyota Motor Corporation No. 1114 3rd! ㅅ (100 cases) ・ρ, 2 :', (1001 sounds) 凉 4' (100 cases)

Claims (1)

【特許請求の範囲】[Claims] 白銑の表面層の一部又は全部を急速加熱して溶融し、急
冷することによりチル化したのち、該白銑を870ない
し1050℃で30分間以上保持してオーステナイト化
処理し、その後急冷し、200ないし400℃で10分
間以上保持して恒温変態処理することを特徴とする高強
度黒心可鍛鋳鉄の製造方法。
Part or all of the surface layer of the white piglet is melted by rapid heating and chilled by rapid cooling, and then the white pigtail is held at 870 to 1050°C for 30 minutes or more to undergo austenitization treatment, and then rapidly cooled. , a method for producing high-strength black-core malleable cast iron, characterized by holding it at 200 to 400° C. for 10 minutes or more to undergo isothermal transformation treatment.
JP9992486A 1986-04-30 1986-04-30 Manufacture of high strength black heat malleable cast iron Pending JPS62256913A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9992486A JPS62256913A (en) 1986-04-30 1986-04-30 Manufacture of high strength black heat malleable cast iron

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9992486A JPS62256913A (en) 1986-04-30 1986-04-30 Manufacture of high strength black heat malleable cast iron

Publications (1)

Publication Number Publication Date
JPS62256913A true JPS62256913A (en) 1987-11-09

Family

ID=14260312

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9992486A Pending JPS62256913A (en) 1986-04-30 1986-04-30 Manufacture of high strength black heat malleable cast iron

Country Status (1)

Country Link
JP (1) JPS62256913A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5837069A (en) * 1997-09-16 1998-11-17 Weyburn-Bartel Inc. Cast iron components and method of making

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5837069A (en) * 1997-09-16 1998-11-17 Weyburn-Bartel Inc. Cast iron components and method of making

Similar Documents

Publication Publication Date Title
US5876523A (en) Method of producing spheroidal graphite cast iron article
JPH0461047B2 (en)
JPS6115930B2 (en)
JPS62256913A (en) Manufacture of high strength black heat malleable cast iron
US4619713A (en) Method of producing nodular graphite cast iron
KR100946129B1 (en) Spherical heat treatment method to soften medium carbon steel quickly
JPH0570685B2 (en)
Strobl et al. Investigation of the diffusion couple ductile cast iron/iron
JPH0617186A (en) Spheroidal graphite cast iron member and manufacture thereof
JPS6383245A (en) Graphite cast iron member and its production
JPS627260B2 (en)
JPS6176612A (en) Manufacture of high strength spheroidal graphite cast iron
JPH09316540A (en) Manufacture of steel for machine structural use for contour induction hardening, excellent in cold forgeability, and manufacture of cold forged part
JP2659352B2 (en) Manufacturing method of Bamikiura graphite cast iron
JPH0688123A (en) Production of spheroidal graphite cast iron and spheroidal graphite cast iron
JP2659354B2 (en) Manufacturing method of tough malleable cast iron
JPS6164814A (en) Production of spheroidal graphite cast iron
JPS626612B2 (en)
JP4495800B2 (en) Induction hardening of cast iron
US3673008A (en) Carbonitriding and other thermal treatment of columbium steels
JPS61149428A (en) Spheroidal graphite cast iron
JPS6386815A (en) Production of steel having excellent cold workability
KR20230094651A (en) Low carbon spherodial alloy steel and method of manufacturing the same
JPH03122250A (en) Iron-base alloy having high vibration-absorbing property and its production
JPH01100218A (en) Manufacture of spheroidal graphite cast-iron product