JPS58120719A - Manufacture of case hardening b steel - Google Patents

Manufacture of case hardening b steel

Info

Publication number
JPS58120719A
JPS58120719A JP194882A JP194882A JPS58120719A JP S58120719 A JPS58120719 A JP S58120719A JP 194882 A JP194882 A JP 194882A JP 194882 A JP194882 A JP 194882A JP S58120719 A JPS58120719 A JP S58120719A
Authority
JP
Japan
Prior art keywords
steel
temperature
heated
coarsening
case hardening
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
JP194882A
Other languages
Japanese (ja)
Other versions
JPS6364495B2 (en
Inventor
Takeshi Inoue
毅 井上
Koji Kaneko
金子 晃司
Masao Toyama
雅雄 外山
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.)
Kobe Steel Ltd
Original Assignee
Kobe Steel 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 Kobe Steel Ltd filed Critical Kobe Steel Ltd
Priority to JP194882A priority Critical patent/JPS58120719A/en
Publication of JPS58120719A publication Critical patent/JPS58120719A/en
Publication of JPS6364495B2 publication Critical patent/JPS6364495B2/ja
Granted legal-status Critical Current

Links

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
    • C21D7/00Modifying the physical properties of iron or steel by deformation
    • C21D7/13Modifying the physical properties of iron or steel by deformation by hot working

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Heat Treatment Of Steel (AREA)

Abstract

PURPOSE:To obtain a case hardening B steel inhibiting the austenitic grains from being made coarse during reheating by heating a steel contg. specified percentages of C, Si, Mn, B, N, SolAl and Ti in iron to a specified temp. and by hot rolling the heated steel. CONSTITUTION:A steel consisting of 0.1-0.3% C, 0.1-0.5% Si, 0.3-2.0% Mn, 0.0005-0.003% B, <=0.0035% N, 0.005-0.1% SolAl, (5XN%+0.02)-0.05% Ti and the balance Fe with impurities or further contg. <=2% Cr and/or <=0.5% Mo is heated to 1,150 deg.C- the A3 point, and the heated steel is hot rolled. The austenitic grains of the resulting case hardening B steel is prevented from being made coarse during carburization or other treatment.

Description

【発明の詳細な説明】 本発明は、低温加熱法で製造される含B肌焼鋼について
浸炭処理特等再加熱時のオーステナイト結晶粒の粗大化
を抑制できる含B肌焼鋼の製造法に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing B-containing case-hardened steel that can suppress coarsening of austenite crystal grains during carburizing and special reheating of B-containing case-hardened steel produced by a low-temperature heating method. It is.

含B鋼は微量のB添加により焼入性を改善できるため安
価な鋼材とする特長を有しているが、Bを有効に作用せ
しめるためには、オーステナイト化時にポロンを7リー
な状態(析出物BNになっていない状態)で存在するこ
とが必要である。このため従来から含B鋼にTlを添加
し、NをTiで固定することが行なわれている。そして
このT」添加はまた結晶粒の微細化にも寄与することと
なっている。
B-containing steel has the advantage of being an inexpensive steel material because its hardenability can be improved by adding a small amount of B. However, in order for B to work effectively, poron must be kept in a 7-li state (precipitated) during austenitization. It is necessary for it to exist in a state where it is not a physical entity (BN). For this reason, it has been conventional practice to add Tl to B-containing steel and fix N with Ti. The addition of T also contributes to the refinement of crystal grains.

ところで近時省エネルギ一対策等として圧延時の鋼材(
ビレット)の加熱温度を1150℃以下(従来は120
0〜1250℃)とする低温加熱が行なわれて来つつあ
る。
By the way, recently as a measure to save energy, steel materials (
billet) heating temperature below 1150°C (previously 120°C)
Low-temperature heating (0 to 1250°C) is becoming increasingly common.

この方法をTI添添加含銅鋼適用することを検討すると
、低温加熱法の場合にはTiN等のT1析出物が鋼中に
溶は込まず凝集することとなるため、再加熱時にオース
テナイト結晶粒が粗大化しやすいことが判明した。
When considering the application of this method to TI-added copper-containing steel, in the case of low-temperature heating, T1 precipitates such as TiN do not melt into the steel and agglomerate, so austenite crystal grains are removed during reheating. It was found that it is easy to become coarse.

本発明は、T+添加含B鋼の低温加熱法における上述の
問題全解決し、浸炭処理等の再加熱時にオーステナイト
結晶粒の粗大化を抑制した含B肌焼鋼を得ることを目的
としてなされたものである。
The present invention has been made with the aim of solving all the above-mentioned problems in the low-temperature heating method for T+-added B-containing steel, and obtaining a B-containing case-hardened steel that suppresses coarsening of austenite crystal grains during reheating such as carburizing treatment. It is something.

0.005〜α1チ、Ti(5XNチ+0.02)〜0
.05%を含み、更に必要に応じてCr 2%以下、M
o015チ以下の1種又は2種を含み、残部鉄及び不純
物からなる鋼材を1150℃〜A3点の温度に加熱した
後、熱間圧延することに%徴とする再加熱時のオーステ
ナイト結晶粒グの粗大化を抑制した含B肌焼鋼の製造法
、である。
0.005~α1chi, Ti(5XNchi+0.02)~0
.. 05%, and if necessary, Cr 2% or less, M
The austenite grain size during reheating is determined by heating a steel material containing one or two of the following O015 and the balance consisting of iron and impurities to a temperature of 1150°C to A3 point and then hot rolling it. This is a method for producing B-containing case-hardened steel that suppresses coarsening of the steel.

本発明において、Ti及びNの含有量及び両者の関係は
重要な意味を有する。
In the present invention, the contents of Ti and N and the relationship between them have important meanings.

すなわちTiiζBの焼入性効果を減するBNの析出を
抑制すべくNO固定のために必要な元素である。理論的
にはNの3.4倍(重量)のTIが存在すればNを固定
できるが、酸化物等となるTiを考えると、TiはNの
5倍必要となる。
That is, it is an element necessary for fixing NO in order to suppress the precipitation of BN which reduces the hardenability effect of TiiζB. Theoretically, N can be fixed if 3.4 times (by weight) of TI exists as N, but when considering Ti in the form of oxides, 5 times as much Ti as N is required.

ところでTiをNの5倍又はそれ以上添加した2種の含
B鋼(第1表)について、圧延前扉熱温度を種々変えて
熱間圧延し、得られた棒鋼ヲ925℃×6時間で浸炭処
理し、オーステナイト結晶粒の粗大化挙動を調べた。そ
の結果を第1図に示す。
By the way, two types of B-containing steels (Table 1) containing 5 times more Ti than N or more were hot-rolled at various pre-rolling door heating temperatures, and the resulting steel bars were rolled at 925°C for 6 hours. After carburizing, the coarsening behavior of austenite grains was investigated. The results are shown in FIG.

第1図から知られるように、Ti含有量がNの約5倍で
ある供試材No、1では低温加熱の場合に結晶粒の粗大
化率(結晶粒度No、が4以下の粗大結晶粒の占める面
積比率)が大きくなり、一方Ti含有量が(N%X5+
α03)%程度と過剰である供試材No、2の場合には
低温加熱においても結晶粒粗大化率がほとんど0であり
、微細結晶粒状態が維持されている。
As is known from Fig. 1, in sample material No. 1, in which the Ti content is about 5 times that of N, when heated at low temperature, the coarse crystal grains with a crystal grain coarsening rate (crystal grain size No. 4) The area ratio occupied by ) increases, while the Ti content increases (N%
In the case of sample materials No. 2, which have an excess of about α03)%, the crystal grain coarsening rate is almost 0 even when heated at low temperature, and the fine crystal grain state is maintained.

この第1図から知られるように、低温加熱法において結
晶粒の微細化を図るためにはT1をNの5倍を越えて過
剰に含有せしめる必要があり、第1図の例からみて、T
1含有量の下限は(0,02+5xN%)チが適当であ
る。一方後述の第3図からも知られるように、介在物型
のTI析出物が多くなり過ぎ、延性、冷間加工性を劣化
せしめることになるので、 Ti含有量の上限はα05
%に抑えるべきである。
As is known from FIG. 1, in order to refine the crystal grains in the low-temperature heating method, it is necessary to contain T1 in excess of five times the amount of N.
The appropriate lower limit of the content is (0.02+5xN%). On the other hand, as can be seen from Figure 3 below, the amount of inclusion-type TI precipitates becomes too large and deteriorates ductility and cold workability, so the upper limit of the Ti content is set at α05.
%.

第1表化学成分(wtチ) 次にNについて述べると、NはBの効果を減するという
点では有害な元素であるが、一方TiNの生成による結
晶粒微細化効果が期待できる。第2図は0.2%C−0
,25%5t−0,9%M n −0,03%A4−0
.02%、又は0.04%Ti−0,0015%B肌焼
鋼についてN含有量を変えて低温加熱法で熱間圧延して
製造した棒鋼についてオーステナイト域に再加熱した場
合の、オーステナイト結晶粒の粗大化温度(結晶粒度N
o。
Table 1 Chemical Composition (wt) Next, referring to N, N is a harmful element in that it reduces the effect of B, but on the other hand, it can be expected to have a crystal grain refinement effect due to the formation of TiN. Figure 2 shows 0.2%C-0
,25%5t-0,9%Mn-0,03%A4-0
.. Austenite crystal grains when steel bars manufactured by hot rolling 02% or 0.04%Ti-0,0015%B case-hardening steel with varying N content using a low-temperature heating method are reheated to the austenite region. Coarsening temperature (grain size N
o.

4以下の粗大粒が面積比率で10%となる 温度)とN
@有量との関係?示す図である。第2図から仰られるよ
うに、Ti含有量が上述の(N%×50、al +→)チ以上であって、しかもN含有量が0.003%
以下の場合にオーステナイト結晶粒の粗大化が相当の高
温まで抑えられる。また第3図は第2図と同様の含B肌
焼鋼についてTi、NO含有量を変えた場合にはTi系
介在物が極めて少なくなることが知られる。
The area ratio of coarse particles of 4 or less is 10% (temperature) and N
@Relationship with quantity? FIG. As shown in Figure 2, the Ti content is greater than or equal to the above (N% x 50, al + →), and the N content is 0.003%.
In the following cases, coarsening of austenite grains can be suppressed up to a considerably high temperature. Furthermore, FIG. 3 shows that when the Ti and NO contents are changed for the same B-containing case hardened steel as in FIG. 2, the amount of Ti-based inclusions is extremely reduced.

次に他の化学成分について述べる。Cは強度付与元素で
あり、α1%以下では必要な強度が得られず、またα3
チ以上では延靭性が劣化するので、C0,1〜0.3%
である。肌焼鋼としてはCα13〜α27チが好適であ
る。siは脱酸剤として使用されα05チ以上必要であ
るが、一方多すぎると延性、冷間加工性が悪くなるので
、上限をα5チとする。
Next, we will discuss other chemical components. C is a strength-imparting element, and if it is less than α1%, the required strength cannot be obtained, and if α3% is less than
C0.1~0.3% as the ductility deteriorates if it exceeds
It is. Suitable case hardening steels are Cα13 to α27. Si is used as a deoxidizing agent and is required to have an amount of α05 or more, but if it is too large, ductility and cold workability deteriorate, so the upper limit is set at α5.

Mnは脱酸・脱硫剤ならびに焼入性向上元素として含有
され、α3チ以上必要であるが、多すぎると偏析による
組織の不均一が生じ、冷間加工性も悪くなるので上限を
20%とする。Bは微量の添加で焼入性を向上させる元
素であシ、00005〜0.0031が適量である。h
(lは脱酸剤として使用され、また結晶粒a細化にも有
効であシ、酸可溶性he(soeAn)として0.00
5〜旧チ が適量である。
Mn is contained as a deoxidizing/desulfurizing agent and a hardenability improving element, and is required in an amount of α3 or more, but if it is too large, the structure will become uneven due to segregation and cold workability will deteriorate, so the upper limit should be set at 20%. do. B is an element that improves hardenability when added in a trace amount, and a suitable amount is 00005 to 0.0031. h
(L is used as a deoxidizing agent and is also effective for grain refinement. 0.00 as acid-soluble he (soeAn)
5 to old chi is an appropriate amount.

本発明では上述の元素の他に必要に応じて強度付与元素
としてCr、Mo  の1種又は2種を含有せしめるこ
とができる。Cr2%以上、MoQ、5%以上ではいず
れも延性、冷間加工性が悪くなる。
In the present invention, in addition to the above-mentioned elements, one or both of Cr and Mo can be contained as strength-imparting elements, if necessary. When Cr is 2% or more and MoQ is 5% or more, ductility and cold workability deteriorate.

上述の化学成分を有する鋼材(ビレット)は低温加熱法
によ多熱間圧延される。加熱温度は省エネルギーの観点
、及び圧延後の組織を微細にするために1150℃以下
にする必要がある。なお加熱温度の下限は完全オーステ
ナイト化の必要からA3点となる。
A steel material (billet) having the above-mentioned chemical composition is multi-hot rolled by a low temperature heating method. The heating temperature needs to be 1150°C or less from the viewpoint of energy saving and to make the structure after rolling fine. Note that the lower limit of the heating temperature is A3 point due to the necessity of complete austenitization.

次に本発明の実施例を比較例と共に示す。Next, examples of the present invention will be shown together with comparative examples.

第2表に示す化学成分を有する鋼材(ビレット) ’e
 1150〜900℃の温度に加熱し熱間圧延により棒
鋼を製造した。これらの棒鋼のTi系介在物の清浄度及
び925℃での浸炭処理後のオーステナイト結晶粒の粗
大化率を第3表に示す。第2表、第3表から知られるよ
うに、本発明である記号D−Jはいずれも本発明に規定
するTi、 N の含有量の条件を満足したものについ
て低温加熱法による熱間圧延を行なったものであシ、浸
炭処理時にオーステナイト結晶粒の粗大化が起っていな
い。
Steel material (billet) having the chemical composition shown in Table 2 'e
A steel bar was produced by heating to a temperature of 1150 to 900°C and hot rolling. Table 3 shows the cleanliness of Ti-based inclusions in these steel bars and the coarsening rate of austenite crystal grains after carburizing at 925°C. As is known from Tables 2 and 3, the symbols D-J, which are the present invention, refer to hot rolling by low temperature heating method for products that satisfy the conditions of Ti and N content stipulated in the present invention. No coarsening of austenite crystal grains occurred during the carburizing process.

第2表化生成分(wt%〕 * ppm 第3表 *925℃での浸炭処理Second table production (wt%) * ppm Table 3 *Carburizing treatment at 925℃

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

第1図は圧延前加熱温度とオーステナイト結晶粒の粗大
化率の関係を示す図、第2図はN含有量とオーステナイ
ト結晶粒の粗大化温度との関係を示す図、第3図はTi
、 N/含有量とTi系介在物の清浄度との関係を示す
図である。 λEyと薊力8表シシ1度 (°C) N舎内量(PP’)
Figure 1 is a diagram showing the relationship between heating temperature before rolling and coarsening rate of austenite crystal grains, Figure 2 is a diagram showing the relationship between N content and coarsening temperature of austenite grains, and Figure 3 is a diagram showing the relationship between coarsening temperature of austenite crystal grains.
, is a diagram showing the relationship between the N/content and the cleanliness of Ti-based inclusions. λEy and power 8 tables 1 degree (°C) Amount of N in the building (PP')

Claims (1)

【特許請求の範囲】 (5XN%+0.02)〜0.05%を含み、残部鉄及
び不純物力)らなる鋼材を1150℃〜A3点の温度に
加熱した後熱間圧延することを特徴とする再加熱時のオ
ーステナイト結晶粒、の粗大化を抑制した含B肌焼鋼の
製造法 Ns+o、az ) 〜α05チヲ含み、更にcr2%
以下、M。 O,5チ  以下の1種又は2種を含み、残部鉄及び不
純物からなる鋼材を1150”C−As点の温度に加熱
した後、熱間圧延することを特徴とする再加熱時のオー
ステナイト結晶粒の粗大化を抑制した含B肌焼鋼の製造
[Claims] A steel material comprising (5XN% + 0.02) to 0.05%, the balance being iron and impurities) is heated to a temperature of 1150°C to A3 point and then hot rolled. Manufacturing method of B-containing case hardened steel that suppresses coarsening of austenite crystal grains during reheating
Below, M. Austenite crystals during reheating, characterized in that a steel material containing one or two of the following, with the balance consisting of iron and impurities, is heated to a temperature of 1150"C-As point and then hot rolled. Manufacturing method of B-containing case-hardened steel that suppresses grain coarsening
JP194882A 1982-01-08 1982-01-08 Manufacture of case hardening b steel Granted JPS58120719A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP194882A JPS58120719A (en) 1982-01-08 1982-01-08 Manufacture of case hardening b steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP194882A JPS58120719A (en) 1982-01-08 1982-01-08 Manufacture of case hardening b steel

Publications (2)

Publication Number Publication Date
JPS58120719A true JPS58120719A (en) 1983-07-18
JPS6364495B2 JPS6364495B2 (en) 1988-12-12

Family

ID=11515824

Family Applications (1)

Application Number Title Priority Date Filing Date
JP194882A Granted JPS58120719A (en) 1982-01-08 1982-01-08 Manufacture of case hardening b steel

Country Status (1)

Country Link
JP (1) JPS58120719A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61253347A (en) * 1985-04-30 1986-11-11 Kobe Steel Ltd Low carbon steel having superior cold workability
JPS63103052A (en) * 1986-10-20 1988-05-07 Daido Steel Co Ltd Case hardening steel for cold forging
JPH02197546A (en) * 1989-01-26 1990-08-06 Kobe Steel Ltd Steel for surface quenching having excellent workability
JPH0347918A (en) * 1989-04-08 1991-02-28 Kobe Steel Ltd Production of b-containing steel
JPH03219043A (en) * 1990-01-23 1991-09-26 Topy Ind Ltd Low carbon boron steel track shoe and its manufacture
JPH116048A (en) * 1997-06-12 1999-01-12 Daihatsu Motor Co Ltd Carburized member and carburizing method for steel containing boron
US6126897A (en) * 1995-08-11 2000-10-03 Sumitomo Metal Industries, Ltd. Carburizing steel and steel products manufactured making use of the carburizing steel
KR20170106462A (en) 2015-01-27 2017-09-20 제이에프이 스틸 가부시키가이샤 Case hardening steel

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61253347A (en) * 1985-04-30 1986-11-11 Kobe Steel Ltd Low carbon steel having superior cold workability
JPS63103052A (en) * 1986-10-20 1988-05-07 Daido Steel Co Ltd Case hardening steel for cold forging
JPH0765140B2 (en) * 1986-10-20 1995-07-12 大同特殊鋼株式会社 Case hardening steel for cold forging
JPH02197546A (en) * 1989-01-26 1990-08-06 Kobe Steel Ltd Steel for surface quenching having excellent workability
JPH0347918A (en) * 1989-04-08 1991-02-28 Kobe Steel Ltd Production of b-containing steel
JPH03219043A (en) * 1990-01-23 1991-09-26 Topy Ind Ltd Low carbon boron steel track shoe and its manufacture
US6126897A (en) * 1995-08-11 2000-10-03 Sumitomo Metal Industries, Ltd. Carburizing steel and steel products manufactured making use of the carburizing steel
JPH116048A (en) * 1997-06-12 1999-01-12 Daihatsu Motor Co Ltd Carburized member and carburizing method for steel containing boron
KR20170106462A (en) 2015-01-27 2017-09-20 제이에프이 스틸 가부시키가이샤 Case hardening steel
US11702716B2 (en) 2015-01-27 2023-07-18 Jfe Steel Corporation Case hardening steel

Also Published As

Publication number Publication date
JPS6364495B2 (en) 1988-12-12

Similar Documents

Publication Publication Date Title
JP3358135B2 (en) High strength steel excellent in sulfide stress cracking resistance and method of manufacturing the same
JPH0421718A (en) Production of high strength steel excellent in sulfide stress cracking resistance
JPS58120719A (en) Manufacture of case hardening b steel
JPS61295356A (en) High strength stainless steel
JPS6145685B2 (en)
JPS63286517A (en) Manufacture of high-tensile steel with low yielding ratio
JPS61279656A (en) Non-heattreated steel for hot forging
JPS6223929A (en) Manufacture of steel for cold forging
JPS6164815A (en) Manufacture of high strength steel excellent in delay breakdown resistance
JPH0250916A (en) Production of low alloy high tension seamless steel pipe having fine grained structure
JPS6137334B2 (en)
JP3246993B2 (en) Method of manufacturing thick steel plate with excellent low temperature toughness
JPS6156235A (en) Manufacture of high toughness nontemper steel
JPH0217608B2 (en)
JPH01319650A (en) Low-decarburization spring steel
JP3267653B2 (en) Manufacturing method of high strength steel sheet
JP2541389B2 (en) Method of manufacturing low yield ratio high strength steel
JP2578598B2 (en) Manufacturing method of low yield ratio steel with excellent sulfide stress corrosion cracking resistance
JPS58120720A (en) Production of tempered steel
JPS609825A (en) Production of tough and hard steel
JPS582244B2 (en) Method for manufacturing thick-walled non-tempered high-strength steel with excellent toughness
JPS6046318A (en) Preparation of steel excellent in sulfide cracking resistance
JP2521547B2 (en) Low-temperature steel manufacturing method
JPS6286122A (en) Production of structural steel having high strength and high weldability
JPH07113126B2 (en) Method for producing stainless steel with excellent resistance to stress corrosion cracking