JP2000063943A - Production of steel for high temperature carburizing and steel for high temperature carburizing obtained by this method - Google Patents

Production of steel for high temperature carburizing and steel for high temperature carburizing obtained by this method

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Publication number
JP2000063943A
JP2000063943A JP23758398A JP23758398A JP2000063943A JP 2000063943 A JP2000063943 A JP 2000063943A JP 23758398 A JP23758398 A JP 23758398A JP 23758398 A JP23758398 A JP 23758398A JP 2000063943 A JP2000063943 A JP 2000063943A
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JP
Japan
Prior art keywords
steel
temperature
less
coarsening
carburizing
Prior art date
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Application number
JP23758398A
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Japanese (ja)
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JP4149576B2 (en
Inventor
Sumie Suda
澄恵 須田
Yoshitake Matsushima
義武 松島
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Kobe Steel Ltd
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Kobe Steel Ltd
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Abstract

PROBLEM TO BE SOLVED: To provide a method for producing steel for high temperature carburizing capable of preventing the coarsening of crystal grains at the time of carburizing treatment. SOLUTION: Steel contg., by mass, 0.001 to 0.1% Nb, 0.001 to 0.1% Al and 0.010 to 0.03% N is heated at the heating temp. T( deg.C) satisfying T>=1000× 1.62×[Nb]+2.28×[N])+1000 ([ ] denotes the content (%) of each element), is thereafter hot-worked and is cooled in the temp. range of the hot working finishing temp. to the A3 transformation point at the average cooling rate of >=30 deg.C/sea.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【発明の属する技術分野】本発明は、高温浸炭用鋼(肌
焼鋼)の製造方法および該方法により得られる高温浸炭
用鋼材に関する。詳細には、冷間鍛造または温間鍛造の
後に浸炭処理する際、オーステナイト結晶粒の粗大化や
異常成長の発生を防止することのできる高温浸炭用鋼の
製造方法、および該方法により得られる高温浸炭用鋼材
に関するものである。
TECHNICAL FIELD The present invention relates to a method for producing high-temperature carburizing steel (case hardening steel) and a high-temperature carburizing steel material obtained by the method. Specifically, when performing carburizing treatment after cold forging or warm forging, a method for producing high-temperature carburizing steel capable of preventing coarsening and abnormal growth of austenite crystal grains, and a high temperature obtained by the method The present invention relates to carburizing steel materials.

【0002】[0002]

【従来の技術】歯車、シャフト、ピン等に用いられる肌
焼鋼は、温間鍛造または冷間鍛造を行った後、浸炭焼入
れ処理するが、こうした一連の熱処理を行う際、鋼材が
高温で長時間加熱される為、オーステナイト結晶粒が粗
大化したり異常成長するという問題がある。オーステナ
イト結晶粒が粗大化等すると、焼入れ硬さのバラツキや
歪みの発生、靭性の低下及び疲労強度の低下といった弊
害を招いてしまう。
BACKGROUND ART Case hardening steel used for gears, shafts, pins and the like is carburized and quenched after warm forging or cold forging. Since it is heated for a time, there are problems that the austenite crystal grains become coarse or abnormally grow. When the austenite crystal grains are coarsened, there are adverse effects such as variations in quenching hardness and strain, deterioration of toughness and deterioration of fatigue strength.

【0003】特に近年では、部品製造コストの低減を狙
って、浸炭時間を短縮する為に高温で浸炭処理する傾向
にある。しかしながら、浸炭温度が高くなるとオーステ
ナイト結晶粒の粗大化が益々発生し易くなる為、上述し
た弊害は一層顕著に見られる様になる。
Particularly in recent years, there has been a tendency to carry out carburizing treatment at a high temperature in order to shorten the carburizing time in order to reduce the cost of manufacturing parts. However, as the carburizing temperature becomes higher, coarsening of the austenite crystal grains is more likely to occur, so that the above-mentioned adverse effects become more prominent.

【0004】一方、鋼材の歩留まり向上を目指して、部
品を冷間鍛造する試みが盛んに行われている。ところ
が、冷間鍛造された部品に浸炭処理すると、たとえ加熱
温度を低くしたとしても、部分的にオーステナイト結晶
粒の粗大化が起こりり易くなり、やはり、焼入れ硬さの
バラツキ等といった上記弊害は避けられない。
On the other hand, attempts have been actively made to cold forge parts in order to improve the yield of steel products. However, when carburizing a cold forged part, even if the heating temperature is lowered, coarsening of austenite crystal grains is likely to occur partially, and the above adverse effects such as variation in quenching hardness are avoided. I can't.

【0005】そこで、オーステナイト結晶粒の粗大化を
抑制し、上述した不具合を回避する為に種々の提案がな
されている。例えば、特公平3−7744には、鋼中の
Al,Nb,N量を抑制することによって表面硬化処理
時の異常粗粒発生を完全に防止すると共に、N含有量の
増加による靱性の低下をAl量の添加で補う方法が;特
開平4−176816には、加工温度等の熱間加工条件
及び加工後の冷却速度を制御する方法が;特公平6−6
3079には、浸炭後に鍛造する方法が、夫々開示され
ている。しかしながら、近年では浸炭温度の上昇や冷間
加工における加工率の上昇を余儀なくされる為、これら
の方法では所望の結晶粒粗大化抑制効果が充分得られな
いことが分かった。
Therefore, various proposals have been made in order to suppress coarsening of austenite crystal grains and avoid the above-mentioned problems. For example, in Japanese Examined Patent Publication No. 3-7744, the generation of abnormal coarse grains during surface hardening treatment is completely prevented by suppressing the amounts of Al, Nb, and N in steel, and the toughness decreases due to the increase in N content. Japanese Patent Laid-Open No. 4-176816 discloses a method of controlling hot working conditions such as working temperature and a cooling rate after working;
No. 3079 discloses a method of forging after carburizing, respectively. However, in recent years, since it has been unavoidable to raise the carburizing temperature and the working rate in the cold working, it has been found that these methods cannot sufficiently obtain the desired grain coarsening suppressing effect.

【0006】[0006]

【発明が解決しようとする課題】本発明は上記事情に着
目してなされたものであり、温間鍛造または冷間鍛造し
た後、浸炭焼入れする浸炭用鋼であって、浸炭処理時に
結晶粒の粗大化を防止することのできる高温浸炭用鋼の
製造方法を提供することにある。
SUMMARY OF THE INVENTION The present invention has been made in view of the above circumstances, and is a carburizing steel which is carburized and quenched after warm forging or cold forging. An object of the present invention is to provide a method for producing high-temperature carburizing steel that can prevent coarsening.

【0007】[0007]

【課題を解決するための手段】上記課題を解決すること
のできた本発明に係る高温浸炭用鋼の製造方法とは、質
量%で(以下、同じ) Nb:0.001〜0.1%,Al:0.001〜0.
1%,N :0.010〜0.03%を含有する鋼を、 T≧1000×{1.62×[Nb]+2.28×[N]}+1
000 (式中、[ ]は各元素の含有量(%)を意味する)を
満足する加熱温度T(℃)で加熱した後、熱間加工し、
次いで、熱間加工終了温度〜A3 変態点の温度範囲を3
0℃/sec以上の平均冷却速度で冷却するところに要
旨を有するものである。
The method for producing a steel for high temperature carburizing according to the present invention, which has been able to solve the above-mentioned problems, is the mass% (hereinafter the same) Nb: 0.001 to 0.1%, Al: 0.001 to 0.
1%, N: Steel containing 0.010 to 0.03%, T ≧ 1000 × {1.62 × [Nb] + 2.28 × [N]} + 1
000 (in the formula, [] means the content (%) of each element), and after heating at a heating temperature T (° C.), hot working,
Next, the temperature range from the hot working finish temperature to the A 3 transformation point is set to 3
The gist is to cool at an average cooling rate of 0 ° C./sec or more.

【0008】その後、更にA3 変態点〜600℃の温度
範囲を0.5℃/sec以下の平均冷却速度で冷却した
り;鋼中に、更にV:1.5%以下(0%を含まな
い),Ti:0.1%以下(0%を含まない),Ta:
0.1%以下(0%を含まない),Zr:0.1%(0
%を含まない),Te:0.1%(0%を含まない),
およびREM:0.1%(0%を含まない)よりなる群
から選択される少なくとも一種を含有することは、高温
浸炭時におけるオーステナイト結晶粒の粗大化抑制作用
が一層向上するので、本発明の好ましい態様である。こ
こで、「平均冷却速度」とは、鋼材表面での平均冷却速
度を意味する。
Thereafter, the temperature range from A 3 transformation point to 600 ° C. is further cooled at an average cooling rate of 0.5 ° C./sec or less; V: 1.5% or less (0% included) in steel. No), Ti: 0.1% or less (not including 0%), Ta:
0.1% or less (not including 0%), Zr: 0.1% (0
%), Te: 0.1% (0% is not included),
And REM: containing at least one selected from the group consisting of 0.1% (not including 0%) further improves the effect of suppressing coarsening of austenite crystal grains during high temperature carburization, and This is the preferred embodiment. Here, the “average cooling rate” means the average cooling rate on the surface of the steel material.

【0009】また、上記方法により製造された高温浸炭
用鋼材も本発明の範囲内に包含される。
The steel material for high temperature carburization produced by the above method is also included in the scope of the present invention.

【0010】[0010]

【発明の実施の形態】本発明者らは、高温浸炭時におけ
るオーステナイト結晶粒の粗大化を充分抑制し得る高温
浸炭用鋼を提供すべく鋭意検討してきた。その結果、N
b、Al、Nの量を適切に制御した鋼を用い、これらの
析出物を固溶させることのできる温度で加熱した後、オ
ーステナイト域では速やかに冷却すれば、上記析出物が
微細分散される為、オーステナイト結晶粒の粗大化を極
めて効率良く防止し得ること;次いで、2相域およびフ
ェライト域の領域を徐冷すれば、ベイナイト組織・マル
テンサイト組織の生成が抑制され、所望のフェライト・
パーライトの混合組織が得られる為、伸線性や冷鍛性が
確保できることを見出し、本発明を完成した。
BEST MODE FOR CARRYING OUT THE INVENTION The present inventors have earnestly studied to provide a high-temperature carburizing steel capable of sufficiently suppressing coarsening of austenite crystal grains during high-temperature carburization. As a result, N
If the steel in which the amounts of b, Al, and N are appropriately controlled is used and the precipitates are heated at a temperature at which they can form a solid solution, and then rapidly cooled in the austenite region, the precipitates are finely dispersed. Therefore, coarsening of austenite crystal grains can be prevented very efficiently; then, by gradually cooling the two-phase region and the ferrite region, the formation of bainite structure / martensite structure is suppressed, and the desired ferrite
Since a mixed structure of pearlite is obtained, it was found that wire drawability and cold forgeability can be secured, and the present invention was completed.

【0011】この様に本発明では、鋼中の成分組成のみ
ならず、熱間加工時における加熱温度、熱間加工後にお
けるオーステナイト域の冷却速度、更には2相域および
フェライト域の冷却速度を制御することにより、高温浸
炭時におけるオーステナイト結晶粒の粗大化を抑制した
ところに最重要ポイントが存在する。鋼中のNb,A
l,Nを適切に制御してこれらの析出物(炭化物、窒化
物、炭窒化物等)を形成せしめ、該析出物を固溶させた
後、鋼中に微細分散させることによりオーステナイト結
晶粒の成長を防止すること自体は公知であり、前述した
従来技術も、この思想を基礎とするものである。しか
し、本発明では、成分組成の制御に加え、更に熱間加工
時における加熱温度、熱間加工後におけるオーステナイ
ト域の冷却速度、或いは2相域およびフェライト域の冷
却速度を所定範囲に制御することにより上記析出物をう
まく微細析出させたところに技術的意義を有するもので
あり、この様な本発明法独自の構成要件は上記従来技術
には開示されておらず、新規である。
As described above, according to the present invention, not only the composition of components in steel, but also the heating temperature during hot working, the cooling rate in the austenite region after hot working, and the cooling rates in the two-phase region and the ferrite region are determined. The most important point lies in the fact that the control suppresses the coarsening of the austenite crystal grains during high temperature carburization. Nb and A in steel
1 and N are appropriately controlled to form these precipitates (carbides, nitrides, carbonitrides, etc.), and these precipitates are solid-solved and then finely dispersed in the steel to form austenite crystal grains. It is known per se to prevent growth, and the above-mentioned prior art is also based on this idea. However, in the present invention, in addition to controlling the component composition, the heating temperature during hot working, the cooling rate in the austenite region after hot working, or the cooling rate in the two-phase region and the ferrite region should be controlled within a predetermined range. Therefore, it has a technical significance in successfully finely depositing the above-mentioned precipitates, and such constitutional features unique to the method of the present invention are not disclosed in the above-mentioned prior art and are novel.

【0012】以下、本発明法を構成する各要件について
説明する。
Each requirement constituting the method of the present invention will be described below.

【0013】Nb:0.001〜0.1% Nbは、鋼中のCやNと結合してNb炭化物,Nb窒化
物,Nb炭窒化物の析出物を生成するが、該析出物が鋼
中に微細分散すると、浸炭加熱時におけるオーステナイ
ト結晶粒の粗大化防止に極めて有効である。この様な作
用を有効に発揮させる為には、Nbを0.001%以上
添加することが必要である。好ましくは0.02%以上
である。しかし、0.1%を超えて過剰に添加すると、
Nb炭窒化物が凝集してしまい、結晶粒粗大化防止に有
効な析出物が減少し、かえって結晶粒粗大化防止温度が
低下してしまう為、上限を0.1%とした。好ましくは
0.05%以下である。
Nb: 0.001 to 0.1% Nb is combined with C and N in steel to form precipitates of Nb carbide, Nb nitride, and Nb carbonitride, and the precipitate is steel. Finely dispersed in it is extremely effective in preventing coarsening of austenite crystal grains during carburizing and heating. In order to exert such an effect effectively, it is necessary to add 0.001% or more of Nb. It is preferably 0.02% or more. However, if added in excess of 0.1%,
The Nb carbonitrides agglomerate and precipitates effective for preventing crystal grain coarsening decrease, and the crystal grain coarsening prevention temperature lowers on the contrary, so the upper limit was made 0.1%. It is preferably 0.05% or less.

【0014】Al:0.001〜0.1% Alは、鋼中のNと結合してAlNを生成するが、この
窒化物は浸炭加熱時におけるオーステナイト結晶粒の成
長防止に有効である。この様な作用を有効に発揮させる
為には、0.001%以上の添加が必要である。好まし
くは0.01%以上である。しかし、0.1%を超えて
添加するとAlNが凝集し、結晶粒の粗大化防止に有効
な析出物が減少してしまい、かえって結晶粒の粗大化防
止温度が低下してしまう。よって、その上限を0.1%
とした。好ましくは0.06%以下である。
Al: 0.001 to 0.1% Al combines with N in steel to form AlN, and this nitride is effective for preventing growth of austenite crystal grains during carburizing and heating. In order to exert such an effect effectively, it is necessary to add 0.001% or more. It is preferably 0.01% or more. However, if added in excess of 0.1%, AlN aggregates and the precipitates effective for preventing the coarsening of the crystal grains decrease, and the temperature for preventing the coarsening of the crystal grains lowers. Therefore, the upper limit is 0.1%
And It is preferably 0.06% or less.

【0015】N:0.010〜0.03% Nは、NbやAlと結合してNbN、NbCN、AlN
の析出物を生成し、オーステナイト結晶粒の成長を抑制
するのに有効な元素である。この様な作用を有効に発揮
する為には、0.010%以上添加することが必要であ
る。しかし、0.03%を超えて過剰に添加すると、鍛
造時や熱間加工時に割れが発生し易くなる為、その上限
を0.03%とした。好ましくは0.025%以下であ
る。
N: 0.010 to 0.03% N combines with Nb or Al to form NbN, NbCN, AlN
Is an element effective in suppressing the growth of austenite crystal grains. In order to effectively exhibit such an effect, it is necessary to add 0.010% or more. However, if added in excess of 0.03%, cracking tends to occur during forging or hot working, so the upper limit was made 0.03%. It is preferably 0.025% or less.

【0016】本発明は、上記元素を必須的に含有し、残
部:Fe及び不可避的不純物からなるものであるが、更
に、高温浸炭時におけるオーステナイト結晶粒の粗大化
防止を目的として、下記元素を少なくとも1種積極的に
含有させることが有効である。
The present invention essentially contains the above elements, and the balance: Fe and unavoidable impurities. Further, the following elements are added for the purpose of preventing coarsening of austenite crystal grains during high temperature carburization. It is effective to positively contain at least one kind.

【0017】V:1.5%以下,Ti:0.1%以下,
Ta:0.1%以下,Zr:0.1%,Te:0.1
%,およびREM:0.1%よりなる群から選択される
少なくとも一種(いずれの元素も0%を含まない)これ
らの元素は、いずれも微細な析出物(炭窒化物等)を生
成し、高温浸炭時におけるオーステナイト結晶粒の粗大
化を抑制するのに有効である。この様な作用を有効に発
揮させる為には、V:0.001%以上,Ti:0.0
01%以上,Ta:0.001%以上,Zr:0.00
1%以上,Te:0.001%以上,REM:0.00
03%以上、夫々添加することが好ましい。しかし、
V:1.5%,Ti:0.1%,Ta:0.1%,Z
r:0.1%,Te:0.1%,REM:0.1%を超
えて添加すると炭窒化物等が凝集・粗大化してしまい、
結晶粒の粗大化防止に有効な析出物の数が少なくなり、
かえって結晶粒粗大化防止温度が低下する為、上記数値
を上限とすることが好ましい。より好ましくは、V:
1.0%以下,Ti:0.05%以下,Ta:0.05
%以下,Zr:0.05%以下,Te:0.05%以
下,REM:0.05%以下である。これらの元素は単
独で添加しても良いし、或いは2種以上を併用しても構
わない。
V: 1.5% or less, Ti: 0.1% or less,
Ta: 0.1% or less, Zr: 0.1%, Te: 0.1
%, And REM: 0.1%
At least one of these elements (which does not contain 0% of any element) produces fine precipitates (carbonitride, etc.) and is effective in suppressing coarsening of austenite crystal grains during high temperature carburization. Is. In order to effectively exhibit such an effect, V: 0.001% or more, Ti: 0.0
01% or more, Ta: 0.001% or more, Zr: 0.00
1% or more, Te: 0.001% or more, REM: 0.00
It is preferable to add each of them in an amount of 03% or more. But,
V: 1.5%, Ti: 0.1%, Ta: 0.1%, Z
If added in excess of r: 0.1%, Te: 0.1%, REM: 0.1%, carbonitrides and the like will aggregate / coarse,
The number of precipitates effective in preventing coarsening of crystal grains is reduced,
On the contrary, since the crystal grain coarsening prevention temperature is lowered, it is preferable to set the above numerical value to the upper limit. More preferably, V:
1.0% or less, Ti: 0.05% or less, Ta: 0.05
% Or less, Zr: 0.05% or less, Te: 0.05% or less, REM: 0.05% or less. These elements may be added alone or in combination of two or more.

【0018】次いで、上記成分組成からなる鋼を、下式
を満足する加熱温度T(℃)で加熱する。
Next, the steel having the above composition is heated at a heating temperature T (° C.) satisfying the following formula.

【0019】T≧1000×{1.62×[Nb]+2.28×
[N]}+1000 (式中、[ ]は各元素の含有量(%)を意味する) 前述した通り、オーステナイト結晶粒の粗大化を防止す
る為には、Nb炭化物、Nb窒化物、Nb炭窒化物の析
出物を微細且つ多量に分散させる必要がある。一般に、
鋳造後に得られるNb析出物は粗大であり、結晶粒粗大
化防止作用に有効な微細析出物は極めて少ない為、該微
細析出物を得る為には、上記のNb析出物を一旦固溶さ
せた後、微細析出させなければならない。本発明者らが
検討したところ、所定の微細析出物を効率良く得る為に
は上記加熱温度T(℃)をうまく制御することが必要で
あること;この加熱温度Tは、[Nb]及び[N]によ
って大きく左右され、これら元素の含有量との関係で設
定することが有効であることが分かった。この様に本発
明では、熱間加工時における加熱温度T(℃)を、[N
b]及び[N]との関係で特定したところにポイントが
ある。
T ≧ 1000 × {1.62 × [Nb] + 2.28 ×
[N]} + 1000 (In the formula, [] means the content (%) of each element) As described above, in order to prevent coarsening of austenite crystal grains, Nb carbide, Nb nitride, Nb carbon It is necessary to disperse the nitride precipitate in a fine and large amount. In general,
The Nb precipitates obtained after casting are coarse, and there are very few fine precipitates effective in preventing grain coarsening. Therefore, in order to obtain the fine precipitates, the Nb precipitates were once solid-dissolved. After that, it has to be finely precipitated. As a result of studies by the present inventors, it is necessary to control the heating temperature T (° C.) well in order to efficiently obtain a predetermined fine precipitate; the heating temperature T is [Nb] and [Nb]. It was found that it is effective to set in relation to the contents of these elements, which is largely influenced by N]. Thus, in the present invention, the heating temperature T (° C.) during hot working is [N
There is a point where it is specified in relation to [b] and [N].

【0020】このことを明らかにする為に、図1にN
b,Nの含有量と加熱温度との関係をグラフ化して示
す。N含有量を夫々、0.010%,0.015%,
0.020%,0.025%に設定した場合における加
熱温度Tの範囲は、鋼中のNb量との関係で決定され、
上記式に基づいて得られるプロット及びその上方域を満
足する温度で加熱した場合に限り、Nb析出物が固溶し
て微細析出することが分かった。
In order to clarify this, in FIG.
The relationship between the contents of b and N and the heating temperature is shown in the form of a graph. N content is 0.010%, 0.015%,
The range of the heating temperature T in the case of setting 0.020% and 0.025% is determined in relation to the amount of Nb in steel,
It was found that Nb precipitates were solid-dissolved and finely precipitated only when the plot obtained based on the above formula and the upper region thereof were heated at a temperature satisfying them.

【0021】この様に上記加熱温度Tで加熱した後、熱
間加工するが、本発明では、熱間加工終了温度〜A3
態点の温度範囲を30℃/sec以上の平均冷却速度で
冷却しなければならない。
After heating at the heating temperature T as described above, hot working is performed, but in the present invention, the temperature range from the hot working finish temperature to the A 3 transformation point is cooled at an average cooling rate of 30 ° C./sec or more. Must.

【0022】Nb炭化物等のNb析出物は、オーステナ
イト域よりもフェライト域(2相域を含む)で析出させ
た方が、微細化し易く、結晶の成長も起こり難い。従っ
て、上記の如く高温で加熱させ、Nb析出物を一旦固溶
させた後、冷却する過程において、オーステナイト域で
Nb炭化物等が析出しない様、冷却速度に留意すること
が非常に重要であり、本発明では、熱間加工終了温度〜
3 変態点の温度範囲を30℃/sec以上の平均冷却
速度で冷却することとした。この様に本発明では、所望
の微細析出物がうまく得られる様、熱間加工における加
熱温度のみならず加工後の冷却速度を細かく制御したと
ころに特徴を有する。好ましくは35℃/sec以上で
ある。尚、その上限は特に限定されないが、実操業レベ
ル等を考慮すれば、100℃/sec以下に制御するこ
とが推奨される。
When Nb precipitates such as Nb carbides are precipitated in the ferrite region (including the two-phase region) rather than in the austenite region, they are more easily miniaturized and crystal growth is less likely to occur. Therefore, it is very important to pay attention to the cooling rate so that Nb carbide or the like does not precipitate in the austenite region in the process of cooling after heating at high temperature as described above, once solid-dissolving the Nb precipitate, and then cooling. In the present invention, the hot working end temperature ~
The temperature range of the A 3 transformation point was set to cool at an average cooling rate of 30 ° C./sec or more. As described above, the present invention is characterized in that not only the heating temperature in hot working but also the cooling rate after working are finely controlled so that a desired fine precipitate can be obtained successfully. It is preferably 35 ° C./sec or more. The upper limit is not particularly limited, but it is recommended to control it to 100 ° C./sec or less in consideration of the actual operation level and the like.

【0023】以上が本発明法の必須工程であるが、更
に、A3 変態点〜600℃の温度範囲を0.5℃/se
c以下の平均冷却速度で冷却することにより、所望のN
b析出物を一層効率良く微細分散させることができる。
即ち、上述した通り、Nb炭化物等のNb析出物はオー
ステナイト域よりもフェライト域(2相域を含む)で析
出させた方が微細な析出物が得られ、結晶の成長も起こ
り難い。また、圧延後にベイナイト組織やマルテンサイ
ト組織が生成すると伸線時に断線が発生したり、冷間加
工性が低下する等の弊害が生じる。この様な弊害を防ぐ
為には、圧延後の組織を均一なフェライト・パーライト
の混合組織にすることが必要であり、その為に上記の温
度範囲を0.5℃/sec以下の冷却速度で徐冷するこ
とにした次第である。
The above are the essential steps of the method of the present invention. Furthermore, the temperature range from the A 3 transformation point to 600 ° C. is 0.5 ° C./se.
By cooling at an average cooling rate of c or less, the desired N
b The precipitate can be finely dispersed more efficiently.
That is, as described above, when Nb precipitates such as Nb carbide are precipitated in the ferrite region (including the two-phase region) rather than in the austenite region, finer precipitates are obtained and crystal growth is less likely to occur. Further, when a bainite structure or martensite structure is formed after rolling, there are problems such as breakage during wire drawing and deterioration of cold workability. In order to prevent such an adverse effect, it is necessary to make the structure after rolling into a uniform mixed structure of ferrite and pearlite. For this reason, the above temperature range is kept at a cooling rate of 0.5 ° C / sec or less. It depends on the slow cooling.

【0024】更に、上述の様にして得られた高温浸炭用
鋼を部品に適用するに当たっては、部品に加工した後、
ガス、真空、プラズマ等による浸炭若しくは浸炭窒化、
または高周波焼入れを行い、必要によりショットピーニ
ング加工してから表面を強化する等の方法を採用するこ
とができる。
Further, when the high temperature carburizing steel obtained as described above is applied to parts, after the parts are processed,
Carburizing or carbonitriding with gas, vacuum, plasma, etc.
Alternatively, it is possible to employ a method in which induction hardening is performed and, if necessary, shot peening is performed and then the surface is strengthened.

【0025】以下、実施例に基づいて本発明を詳細に述
べる。ただし、下記実施例は本発明を制限するものでは
なく、前・後記の趣旨を逸脱しない範囲で変更実施する
ことは本発明の技術的範囲に包含される。
The present invention will be described in detail below based on examples. However, the following examples do not limit the present invention, and it is within the technical scope of the present invention to make changes and modifications without departing from the spirit of the above and the following.

【0026】[0026]

【実施例】表1に示す化学組成の鋼材を溶製し、一辺が
155mmの正方形ビレットに分塊圧延した後、種々の
加熱温度に加熱し、φ19mm線材に圧延した。圧延後
直ちにA3 変態点までの温度範囲を種々の冷却速度で冷
却した後、更にA3 変態点から600℃までの温度範囲
につき、冷却速度を変化させて冷却した。圧延後の組
織、および測定した硬さの結果を表2に示す。
EXAMPLE Steel materials having the chemical compositions shown in Table 1 were melted, slab-rolled into a square billet having a side length of 155 mm, heated to various heating temperatures, and rolled into a φ19 mm wire rod. Immediately after rolling, the temperature range up to the A 3 transformation point was cooled at various cooling rates, and then the temperature range from the A 3 transformation point to 600 ° C. was changed by changing the cooling rate. Table 2 shows the structure after rolling and the result of the measured hardness.

【0027】その後、各供試材を減面率30%で伸線加
工した後、図2に示す熱処理条件で球状化焼鈍(750
℃×7Hr→650℃まで炉冷)を行い、引続き減面率
10%のスキンパス加工、更に加工率50%の冷間押出
し加工を行った。次いで、図3に示す如く900〜11
00℃に加熱して3時間保持した後、水焼入れ処理し
た。
After that, each test material was wire-drawn at a surface reduction rate of 30%, and then spheroidized (750) under the heat treatment conditions shown in FIG.
(° C × 7 Hr → furnace cooling to 650 ° C.), followed by skin pass processing with a surface reduction rate of 10% and cold extrusion processing with a processing rate of 50%. Then, as shown in FIG.
After heating to 00 ° C. and holding for 3 hours, water quenching treatment was performed.

【0028】この様にして得られた各焼入れ材の結晶粒
度につき、各加熱温度でのオーステナイト結晶粒度(J
IS G 0551)を測定し、結晶粒5番以上の整細
粒である限界の温度を粗大化温度とした。
With respect to the grain size of each of the quenched materials thus obtained, the austenite grain size (J
IS G 0551) was measured, and the critical temperature at which the crystal grains were fine grains of size 5 or more was defined as the coarsening temperature.

【0029】これらの結果を表2に併記する。The results are also shown in Table 2.

【0030】[0030]

【表1】 [Table 1]

【0031】[0031]

【表2】 [Table 2]

【0032】表より以下の様に考察することができる。The following can be considered from the table.

【0033】No.1〜9は、本発明の要件を満足する本
発明例であるが、いずれも粗大化温度は975℃以上と
極めて高く、断線も全く見られなかった。
Nos. 1 to 9 are examples of the present invention satisfying the requirements of the present invention, but in all of them, the coarsening temperature was extremely high at 975 ° C. or higher, and no disconnection was observed.

【0034】これに対し、本発明のいずれかの要件を満
足しないNo.10〜16は、夫々以下の不具合を伴って
いる。
On the other hand, Nos. 10 to 16 which do not satisfy any of the requirements of the present invention are accompanied by the following problems.

【0035】No.10はNb無添加鋼であり、高温での
結晶粒粗大化防止に有効な微細析出物の析出量が少ない
為、低温でも結晶粒の粗大化が発生した。
No. 10 is a Nb-free steel, and the amount of fine precipitates effective for preventing crystal grain coarsening at high temperatures was small, so that coarsening of crystal grains occurred even at low temperatures.

【0036】No.11はNbの添加量が多い例であり、
Nb炭化物、Nb窒化物、Nb炭窒化物の凝集が起こっ
て析出物が粗大化する為、所望の微細析出物が少なくな
り、低温でも結晶粒の粗大化が発生した。
No. 11 is an example in which the amount of Nb added is large,
Aggregation of Nb carbide, Nb nitride, and Nb carbonitride occurs to coarsen the precipitate, so that desired fine precipitates are reduced, and coarsening of crystal grains occurs even at low temperature.

【0037】No.12はAlの添加量が多い例であり、
AlNの凝集が起こって析出物が粗大化する為、目的と
する微細析出物が少なくなり、低温でも結晶粒の粗大化
が見られた。
No. 12 is an example in which a large amount of Al is added,
Since agglomeration of AlN occurred and the precipitate was coarsened, the desired fine precipitate was reduced, and the coarsened crystal grains were observed even at low temperature.

【0038】No.13はNの添加量が少ない例であり、
Nb窒化物、Nb炭窒化物、AlNの析出量が少ない
為、低温でも結晶粒の粗大化が発生した。
No. 13 is an example in which the amount of N added is small,
Since the precipitation amounts of Nb nitride, Nb carbonitride, and AlN were small, coarsening of crystal grains occurred even at low temperatures.

【0039】No.14は、熱間加工時における加熱温度
Tが本発明で特定する範囲を外れる例であり、熱間加工
前に存在したNb析出物が十分に固溶せず、粗大なまま
残っている為、熱間加工後の析出物が少なくなり、低温
でも結晶粒の粗大化が見られた。
No. 14 is an example in which the heating temperature T during hot working is out of the range specified in the present invention, and the Nb precipitates existing before hot working do not sufficiently form a solid solution and remain coarse. Since it remained, the amount of precipitates after hot working decreased, and coarsening of crystal grains was observed even at low temperature.

【0040】No.15は、熱間加工終了後A3 変態点ま
での冷却速度が遅い例であり、オーステナイト域でNb
炭化物、Nb窒化物、Nb炭窒化物の析出・成長が起こ
って微細析出物量が少なくなる為、低温でも結晶粒の粗
大化が発生した。
No. 15 is an example in which the cooling rate up to the A 3 transformation point after completion of hot working is slow, and Nb in the austenite region.
Precipitation / growth of carbides, Nb nitrides, and Nb carbonitrides occurred and the amount of fine precipitates decreased, so that coarsening of crystal grains occurred even at low temperatures.

【0041】No.16は、熱間加工終了後、A3 変態点
〜600℃の温度範囲を、本発明の好ましい冷却速度を
超えて冷却した例であり、圧延後の組織が(フェライト
+パーライト+ベイナイト)の混合組織となる為、伸線
加工の際、断線が発生してしまい、部品に加工すること
ができなかった。
No. 16 is an example in which after the hot working, the temperature range of A 3 transformation point to 600 ° C. was cooled beyond the preferable cooling rate of the present invention, and the structure after rolling was (ferrite + pearlite). Since it has a mixed structure of + bainite), wire breakage occurred during wire drawing, and it could not be processed into parts.

【0042】[0042]

【発明の効果】本発明は以上の様に構成されており、鋼
中の化学成分および熱間加工時の熱処理条件を制御する
ことによって、浸炭焼入れ時に高温まで結晶粒の粗大化
が生成しない鋼、即ち粗大化温度の高い高温浸炭用鋼を
効率良く提供することができた。
EFFECTS OF THE INVENTION The present invention is configured as described above, and by controlling the chemical composition in steel and the heat treatment conditions during hot working, steel that does not cause coarsening of crystal grains up to high temperatures during carburizing and quenching That is, it was possible to efficiently provide high-temperature carburizing steel having a high coarsening temperature.

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

【図1】Nb,Nの含有量と加熱温度との関係を示すグ
ラフである
FIG. 1 is a graph showing the relationship between Nb and N contents and heating temperature.

【図2】実施例で用いた球状化焼鈍処理を説明する概略
図である。
FIG. 2 is a schematic diagram illustrating a spheroidizing annealing process used in Examples.

【図3】実施例で用いた熱処理パターンを示す概略図で
ある。
FIG. 3 is a schematic diagram showing a heat treatment pattern used in Examples.

───────────────────────────────────────────────────── フロントページの続き Fターム(参考) 4K032 AA01 AA05 AA16 AA19 AA21 AA22 AA31 AA33 AA34 AA35 AA36 AA39 AA40 BA02 CB02 CD01 CD03 CF02 CG02 CH05 CH06 CJ05    ─────────────────────────────────────────────────── ─── Continued front page    F term (reference) 4K032 AA01 AA05 AA16 AA19 AA21                       AA22 AA31 AA33 AA34 AA35                       AA36 AA39 AA40 BA02 CB02                       CD01 CD03 CF02 CG02 CH05                       CH06 CJ05

Claims (4)

【特許請求の範囲】[Claims] 【請求項1】質量%で(以下、同じ) Nb:0.001〜0.1%,Al:0.001〜0.
1%,N :0.010〜0.03%を含有する鋼を、 T≧1000×{1.62×[Nb]+2.28×[N]}+1
000 (式中、[ ]は各元素の含有量(%)を意味する)を
満足する加熱温度T(℃)で加熱した後、熱間加工し、 熱間加工終了温度〜A3 変態点の温度範囲を30℃/s
ec以上の平均冷却速度で冷却することを特徴とする高
温浸炭用鋼の製造方法。
1. In mass% (hereinafter the same), Nb: 0.001 to 0.1%, Al: 0.001 to 0.
1%, N: Steel containing 0.010 to 0.03%, T ≧ 1000 × {1.62 × [Nb] + 2.28 × [N]} + 1
000 (wherein, [] means the content of each element (%)) was heated at a heating temperature T (° C.) which satisfies, hot worked, the hot working finishing temperature to A 3 transformation point Temperature range is 30 ℃ / s
A method for producing high-temperature carburizing steel, which comprises cooling at an average cooling rate of ec or more.
【請求項2】 更に、A3 変態点〜600℃の温度範囲
を0.5℃/sec以下の平均冷却速度で冷却するもの
である請求項1に記載の製造方法。
2. The manufacturing method according to claim 1, further comprising cooling in a temperature range from A 3 transformation point to 600 ° C. at an average cooling rate of 0.5 ° C./sec or less.
【請求項3】 鋼中に、更に V :1.5%以下(0%を含まない),Ti :
0.1%以下(0%を含まない),Ta :0.1%以
下(0%を含まない),Zr :0.1%以下(0%を
含まない),Te :0.1%以下(0%を含まな
い),およびREM:0.1%以下(0%を含まない)
よりなる群から選択される少なくとも一種を含有するも
のである請求項1または2に記載の製造方法。
3. V: 1.5% or less (not including 0%), Ti:
0.1% or less (not including 0%), Ta: 0.1% or less (not including 0%), Zr: 0.1% or less (not including 0%), Te: 0.1% or less (0% is not included), and REM: 0.1% or less (0% is not included)
The manufacturing method according to claim 1 or 2, which contains at least one selected from the group consisting of:
【請求項4】 請求項1〜3のいずれかに記載の方法に
より製造された高温浸炭用鋼材。
4. A steel material for high-temperature carburizing produced by the method according to claim 1.
JP23758398A 1998-08-24 1998-08-24 Method for producing high-temperature carburizing steel and high-temperature carburizing steel obtained by the method Expired - Fee Related JP4149576B2 (en)

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003027135A (en) * 2001-07-10 2003-01-29 Aichi Steel Works Ltd Method for producing steel for high temperature carburization, and steel for high temperature carburization produced by the method
JP2010222634A (en) * 2009-03-23 2010-10-07 Kobe Steel Ltd Case hardening steel superior in properties of reducing size of maximum crystal grain and manufacturing method therefor
JP2020094236A (en) * 2018-12-12 2020-06-18 日本製鉄株式会社 Carburized component, shaped material for carburized component, and method for producing same

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2003027135A (en) * 2001-07-10 2003-01-29 Aichi Steel Works Ltd Method for producing steel for high temperature carburization, and steel for high temperature carburization produced by the method
JP4681160B2 (en) * 2001-07-10 2011-05-11 愛知製鋼株式会社 Manufacturing method of high temperature carburizing steel and high temperature carburizing steel manufactured by the method
JP2010222634A (en) * 2009-03-23 2010-10-07 Kobe Steel Ltd Case hardening steel superior in properties of reducing size of maximum crystal grain and manufacturing method therefor
JP2020094236A (en) * 2018-12-12 2020-06-18 日本製鉄株式会社 Carburized component, shaped material for carburized component, and method for producing same
JP7200646B2 (en) 2018-12-12 2023-01-10 日本製鉄株式会社 CARBURIZED PARTS, MATERIALS FOR CARBURIZED PARTS, AND PRODUCTION METHOD THEREOF

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