JPS63162811A - Manufacture of precipitation-hardening steel - Google Patents

Manufacture of precipitation-hardening steel

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Publication number
JPS63162811A
JPS63162811A JP30890786A JP30890786A JPS63162811A JP S63162811 A JPS63162811 A JP S63162811A JP 30890786 A JP30890786 A JP 30890786A JP 30890786 A JP30890786 A JP 30890786A JP S63162811 A JPS63162811 A JP S63162811A
Authority
JP
Japan
Prior art keywords
weight
steel
hot
precipitation
hardness
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
JP30890786A
Other languages
Japanese (ja)
Inventor
Akihiro Matsuzaki
明博 松崎
Hiroshi Otsubo
宏 大坪
Yutaka Oka
裕 岡
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.)
JFE Steel Corp
Original Assignee
Kawasaki Steel 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 Kawasaki Steel Corp filed Critical Kawasaki Steel Corp
Priority to JP30890786A priority Critical patent/JPS63162811A/en
Publication of JPS63162811A publication Critical patent/JPS63162811A/en
Pending legal-status Critical Current

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  • Heat Treatment Of Steel (AREA)

Abstract

PURPOSE:To manufacture a precipitation hardening-type structural steel improved in crimping workability, by heating a steel containing specific percentages of C, Si, Mn, Ni, Mo, Cu, and Al and by subjecting the above steel to hot working and aging treatment under specific conditions and then to cooling. CONSTITUTION:The steel containing, by weight, 0.05-0.20% C, 0.1-2.0% Si, 0.5-2.1% Mn, 0.5-3.5% Ni, 0.05-0.6% Mo, 0.5-2.0% Cu, and 0.4-1.5% Al is heated up to about 950-1,300 deg.C. Subsequently, without being hot-rolled or after hot-rolled, the above steel is hot-worked at 700-900 deg.C at 10-40% draft, held at 450-550 deg.C for 1-100hr to undergo aging treatment, and then cooled. In this way, the precipitation-hardening steel improved in crimping workability and used for metal mold for plastic molding can be obtained.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、金型とくにプラスチック成型用金型が主たる
使途である析出硬化型構造用鋼の製造方法に関するもの
である。
DETAILED DESCRIPTION OF THE INVENTION (Industrial Application Field) The present invention relates to a method for manufacturing precipitation hardening structural steel, which is mainly used as a mold, particularly a plastic mold.

(従来の技術) 従来、プラスチック成形用の金型には、−殻構造用炭素
鋼(JIS−3C,SS等)、低合金鋼(JIS−S0
M改良鋼)、高合金@ (JIS−SKD、 SO5等
)が使用されてきた。特に、大型のプラスチック成型用
金型材料としては、主としてコストの観点から、−殻構
造用炭素鋼および低合金鋼(SCM系)が主流であった
(Prior art) Conventionally, molds for plastic molding are made of carbon steel for shell structure (JIS-3C, SS, etc.), low alloy steel (JIS-S0
M improved steel), high alloy @ (JIS-SKD, SO5, etc.) have been used. In particular, carbon steel for shell structures and low alloy steel (SCM type) have been the mainstream as mold materials for large-sized plastic molding, mainly from the viewpoint of cost.

近年、プラスチック製品の大型化に伴い、使用される金
型も必然的に厚肉のものが必要となってきた。ところが
、前記−殻構造用炭素鋼は、肉厚数百間までは製造可能
であるが、硬さがHv 200程度と低いために型の寿
命が短いという欠点があった。
In recent years, as plastic products have become larger, the molds used have inevitably become thicker. However, although the above-mentioned carbon steel for shell structures can be manufactured to a wall thickness of several hundred centimeters, the hardness is as low as about 200 Hv, so the mold life is short.

そのため、従来より高寿命を要求される場合には、Hv
 300前後を確保できる低合金@ (SCM系)が使
用されていた。しかし、SCM系鋼は、肉厚が200 
mmを越えるとフェライト相が生成するようになり、よ
り厚肉になった場合の硬さの確保が困難であるとともに
、硬さは冷却速度に大きく依存するだめに均一性の点で
も問題が生じていた。更に、SCM系鋼は高C鋼である
ため、溶接性が悪い。金型には、設計変更、補修等のた
めに頻繁に溶接が施されるため、溶接前後の加熱作業、
溶接割れを軽減できる金型材料が望まれている。
Therefore, when a longer life than before is required, Hv
Low alloy @ (SCM type) that can secure around 300 was used. However, SCM steel has a wall thickness of 200 mm.
If the thickness exceeds mm, a ferrite phase will begin to form, making it difficult to ensure hardness when the wall becomes thicker, and problems will also arise in terms of uniformity since hardness is largely dependent on the cooling rate. was. Furthermore, since SCM steel is a high C steel, weldability is poor. Molds are frequently welded for design changes, repairs, etc., so heating work before and after welding,
A mold material that can reduce weld cracking is desired.

また、従来提案されている析出硬化型鋼の場合、溶接し
たときに熱影響部(HAZ)に軟化域が生成し、このH
AZが母材に比べてビッカース硬さで 100以上も低
くなる。従って、通常は数時間の後熱処理(時効処理を
兼ねる)により、これらの軟化域を再硬化し、略母材に
近い硬さに調整する処理を行っていた。しかしながら、
大型の金型に限って見ると、上記後熱処理は困難である
In addition, in the case of precipitation hardening steels that have been proposed so far, a softening region is generated in the heat affected zone (HAZ) when welding, and this HAZ
The Vickers hardness of AZ is more than 100 lower than that of the base material. Therefore, normally, these softened regions are re-hardened by post-heat treatment (which also serves as aging treatment) for several hours, and the hardness is adjusted to approximately that of the base material. however,
When considering only large molds, the above-mentioned post-heat treatment is difficult.

そこで、最近では、硬さおよび溶接性を改善し、特に溶
接のままでもHAZ部の硬さが母材と略同等の特性を示
し、特にプラスチック鋳造品の大型化に伴う厚肉の金型
材に使用しても前述した困難を解決し得る鋼材の開発が
望まれている。この点、溶接性や放電加工性を改良した
従来の時効硬化型プラスチック金型用鋼の場合、低C化
にあわせてCu、AI!、およびNiを添加し、時効析
出により強度を確保している。しかし、Cu、 Niは
焼入性向上元素でもあるため、これらの元素を低減して
コスト減を図った場合には、時効前の組織にフェライト
が生成しやすくなり、時効化性が阻害される。このこと
は大型のプラスチック金型用鋼では加熱後の冷却速度が
極めて遅くなるために致命的欠陥となる。また、溶接部
の硬さが不均一になることから、後熱処理を施さなけれ
ばならず、大型のプラスチック金型用鋼としては大きな
欠点となっていた。
Therefore, recently, we have improved the hardness and weldability, and in particular, the hardness of the HAZ part shows almost the same characteristics as the base metal even as welded, and it is especially suitable for thick mold materials as plastic casting products increase in size. It is desired to develop a steel material that can solve the above-mentioned difficulties even when used. In this regard, in the case of conventional age-hardening plastic mold steels with improved weldability and electrical discharge machinability, Cu, AI! , and Ni are added to ensure strength through aging precipitation. However, Cu and Ni are also elements that improve hardenability, so when reducing costs by reducing these elements, ferrite tends to form in the structure before aging, which inhibits aging properties. . This is a fatal flaw in steel for large plastic molds because the cooling rate after heating is extremely slow. Furthermore, since the hardness of the welded part becomes uneven, post-heat treatment must be performed, which is a major drawback when used as steel for large plastic molds.

(発明が解決しようとする問題点) 上記問題点を解決するために、−〇の微量添加が、Cu
、 Ni、 Al21が少ない場合でも大型金型用鋼と
して十分に遅い冷却速度でもベイナイト組織を確保し、
時効硬化に寄与するという知見の基に、C:0.05〜
0.20重量%、 Si : 0.1〜2.0重量%、
Mn:0.5〜2.1重量%、 Ni : 0.5〜1
.4重景%重量o:0.05〜0.6重量%、 Cu 
: 0.5〜2.0重量%、 Af :0.4〜1.5
重量%を含む時効硬化型構造用鋼を開発した。
(Problems to be solved by the invention) In order to solve the above problems, the addition of a trace amount of -〇
Even when , Ni, and Al21 are low, the bainite structure is secured even at a sufficiently slow cooling rate as a steel for large molds,
Based on the knowledge that it contributes to age hardening, C: 0.05~
0.20% by weight, Si: 0.1-2.0% by weight,
Mn: 0.5-2.1% by weight, Ni: 0.5-1
.. 4-layered view% weight o: 0.05-0.6% by weight, Cu
: 0.5-2.0% by weight, Af: 0.4-1.5
We have developed an age-hardening structural steel containing %wt.

上記析出硬化型構造用鋼は、ε−Cu相とNiA l相
の析出による相乗効果を利用したものであるが、通常は
熱間加工し、溶体化後、時効処理が施される。しかしな
がら、上記熱処理工程では、溶体化処理した後に時効処
理をするために、再度加熱することになり、コストアッ
プとなる。また、処理後の冷却速度が速し)場合には、
マルテンサイトとベイナイトの2相組織となり、前記析
出硬化型鋼を、例えばプラスチック金型として使用する
場合にはシボ加工性の低下を招く。
The above-mentioned precipitation hardening structural steel utilizes the synergistic effect of the precipitation of the ε-Cu phase and the NiAl phase, and is usually hot-worked, solution-treated, and then subjected to aging treatment. However, in the above-mentioned heat treatment step, in order to perform an aging treatment after the solution treatment, heating is required again, which increases the cost. In addition, if the cooling rate after processing is faster),
This results in a two-phase structure of martensite and bainite, which leads to a decrease in texturability when the precipitation hardening steel is used, for example, as a plastic mold.

本発明の目的は、熱処理工程において再加熱を省略して
製造コストを低減すると共に、マルテンサイトの生成を
抑制してベイナイト相組織にすることによりシボ加工性
を改善することにある。
An object of the present invention is to reduce manufacturing costs by omitting reheating in the heat treatment process, and to improve texturing property by suppressing the formation of martensite and creating a bainite phase structure.

(問題点を解決するための手段) 本発明は、C: 0.05〜0.20重量%、Si:0
.1〜2.0重量%、 Mn : 0.5〜2.1重量
%、 Ni :0.5〜3.5重量%、 Mo : 0
.05〜0.6重量%、Cu : 0.5〜2.0重量
%、Affi:0.4〜1.5重量%を含有する鋼を加
熱し、熱間圧延を経ず又は熱間圧延した後、700〜9
00 ”Cの温度範囲で10〜40%の加工を施し、そ
の後450〜550℃の温度範囲に1〜100時間保持
した後、冷却することを特徴とする析出硬化鋼の製造方
法、 とすることで前述した問題点を解決した。
(Means for solving the problems) The present invention provides C: 0.05 to 0.20% by weight, Si: 0
.. 1 to 2.0% by weight, Mn: 0.5 to 2.1% by weight, Ni: 0.5 to 3.5% by weight, Mo: 0
.. Steel containing 0.05 to 0.6% by weight, Cu: 0.5 to 2.0% by weight, and Affi: 0.4 to 1.5% by weight was heated and hot rolled or not hot rolled. After, 700~9
A method for producing precipitation hardened steel, characterized in that the steel is processed by 10 to 40% in a temperature range of 0.00"C, then held in a temperature range of 450 to 550C for 1 to 100 hours, and then cooled. solved the problems mentioned above.

(作 用) 本発明者等は、C: 0.09重量%、 Si : 0
.41重量%、Mn:1.3重量%、Ni:1.3重量
%、 Mo : 0.41重量%、Cu:1.4重量%
、Affi:0.7重量%を含有する鋼を真空溶解後、
第1図に示すパターンに従い、1200℃に加熱後、’
100ffllllの厚さに予備圧延し、1時間保持後
、1050’C以上の温度域で50%の圧下を加えた後
、種々の温度(’r+)で、圧下率3%。
(Function) The present inventors have determined that C: 0.09% by weight, Si: 0
.. 41% by weight, Mn: 1.3% by weight, Ni: 1.3% by weight, Mo: 0.41% by weight, Cu: 1.4% by weight
, Affi: After vacuum melting steel containing 0.7% by weight,
Following the pattern shown in Figure 1, after heating to 1200℃,'
Pre-rolling to a thickness of 100ffllll, holding for 1 hour, applying a 50% reduction in a temperature range of 1050'C or higher, and then applying a reduction of 3% at various temperatures ('r+).

7%、13%、20%の一パス圧延を行い、種々の保持
温度(T2)で3時間保持後、冷却する熱処理を行なっ
た。
One-pass rolling was performed at 7%, 13%, and 20%, and heat treatment was performed by holding at various holding temperatures (T2) for 3 hours and then cooling.

上述の熱処理工程で得られた鋼と、第2図に示す通常の
溶体化一時効処理で得られたHRC=30゜ベイナイl
−ff190%の鋼とを比較した結果を第38〜3d図
に示す。第3a図は上記T、における圧下率が3%の結
果を、第3b図はT1における圧下率が7%の結果を、
第3c図はT1における圧下率が13%の結果を、第3
d図はT1における圧下率が20%の結果を示すもので
あり、各図中のO印は通常の溶体化一時効処理(以下、
通常の熱処理という)材と比較してベイナイト量が同等
であることを示すものであり、Δ印は通常の熱処理に比
較してベイナイト量が多いことを示しており、黒い印は
、硬さが通常の熱処理に比較して同等以上であることを
示しており、0印は、硬さが通常の熱処理に比較して低
いことを示している。各図からも判るように、圧延温度
(T、)の温度範囲が700〜900℃で10%以上の
圧延を行い、更に保持温度(T2)を450〜550℃
にした場合に、通常の熱処理で得られた鋼と比較して、
ベイナイト−相に近い組織が得られ、機械的性質も同等
になっていることが判る。
The steel obtained by the above heat treatment process and the HRC = 30° bainyl obtained by the normal solution temporary treatment shown in Fig. 2.
The results of comparison with -ff190% steel are shown in Figures 38 to 3d. Figure 3a shows the results when the rolling reduction rate at T is 3%, and Figure 3b shows the results when the rolling reduction rate at T1 is 7%.
Figure 3c shows the results when the rolling reduction rate at T1 is 13%, and
Figure d shows the results when the rolling reduction rate at T1 is 20%, and the O mark in each figure indicates the normal solution temporary treatment (hereinafter referred to as
This indicates that the amount of bainite is the same as that of the normal heat-treated material, and the Δ mark indicates that the amount of bainite is greater than that of the normal heat-treated material, and the black mark indicates that the hardness has increased. This indicates that the hardness is equivalent to or higher than that of normal heat treatment, and the 0 mark indicates that the hardness is lower than that of normal heat treatment. As can be seen from each figure, 10% or more rolling is performed at a rolling temperature (T, ) of 700 to 900°C, and the holding temperature (T2) is 450 to 550°C.
compared to steel obtained by normal heat treatment,
It can be seen that a structure close to a bainite phase was obtained, and the mechanical properties were also the same.

即ち、本発明は、熱間圧延後の適切な熱間加工時の歪み
により、ベイナイト変態とε−Cu相およびN1Aj!
相の析出を促進させて、マルテンサイトを低下させ、ベ
イナイト−相の組織にすることが可能となる。そのため
には、700〜900℃の温度範囲で10〜40%の熱
間加工を施した後、直ちに450〜550℃の温度範囲
に保持した後、冷却することが必要条件となる。
That is, the present invention achieves bainite transformation, ε-Cu phase, and N1Aj! by appropriate strain during hot working after hot rolling.
By promoting phase precipitation, it is possible to reduce martensite and create a bainite phase structure. For this purpose, it is necessary to perform 10 to 40% hot working in a temperature range of 700 to 900°C, immediately maintain the temperature in a temperature range of 450 to 550°C, and then cool it.

以下、本発明の成分と製造条件の限定理由について述べ
る。
The reasons for limiting the components and manufacturing conditions of the present invention will be described below.

CTCは、焼入性および焼入相の硬さを確保するために
必要な元素であり、そのためには0.05重量%以上必
要である。しかし、多過ぎると溶接性、放電加工性等を
阻害するために、上限は0.20重量%とする。
CTC is an element necessary to ensure hardenability and hardness of the hardened phase, and for this purpose, it is required in an amount of 0.05% by weight or more. However, if it is too large, weldability, electrical discharge machinability, etc. will be impaired, so the upper limit is set to 0.20% by weight.

Si : Stは、鋼の脱酸元素として用いるものであ
って0.1重量%以上必要である。しかし、多過ぎると
、延性及び靭性を劣化させるために上限は2.0重量%
とする。
Si: St is used as a deoxidizing element for steel and is required in an amount of 0.1% by weight or more. However, if the amount is too high, the ductility and toughness will deteriorate, so the upper limit is 2.0% by weight.
shall be.

Mn : Mnは、溶体化処理後の時効硬さを高めるた
めに、0.5重量%以上添加するが、あまり多過ぎると
溶接性および熱間加工性を阻害するので、上限は2.1
重量%とする。
Mn: Mn is added in an amount of 0.5% by weight or more in order to increase the aging hardness after solution treatment, but if it is too large, weldability and hot workability are inhibited, so the upper limit is 2.1%.
Weight%.

Ni : Niは、焼入性の向上、Cuの粒界析出によ
る熱間加工性低減の防止、ベイナイト相中にA2と共存
したN1Affi相を析出することによる時効硬化に寄
与する。そのためには、0.5重量%以上添加する必要
があるが、過剰に添加すると、硬さの上昇および溶接部
の硬さの差が大きくなり過ぎるため、上限は3.5重量
%とする。
Ni: Ni improves hardenability, prevents reduction in hot workability due to grain boundary precipitation of Cu, and contributes to age hardening by precipitating N1Affi phase coexisting with A2 in the bainite phase. For this purpose, it is necessary to add 0.5% by weight or more, but if added in excess, the hardness will increase and the difference in hardness of the weld will become too large, so the upper limit is set to 3.5% by weight.

Mo : Moは、焼入性および析出硬化に寄与する元
素であり、そのためには0.05重重景以上添加する必
要がある。一方、多過ぎるとコスト増となるために、上
限は0.6重量%とする。
Mo: Mo is an element that contributes to hardenability and precipitation hardening, and for this purpose it is necessary to add 0.05% or more. On the other hand, if it is too large, the cost will increase, so the upper limit is set to 0.6% by weight.

Cu : Cuは、ベイナイト組織中にε−Cu相とし
て析出して時効硬化に寄与するので、0.5重量%以上
添加する必要がある。しかし、余り多過ぎると熱間加工
性を阻害するために、上限は2.0重量%とする。
Cu: Cu precipitates as an ε-Cu phase in the bainite structure and contributes to age hardening, so it is necessary to add 0.5% by weight or more. However, if the content is too large, hot workability will be inhibited, so the upper limit is set to 2.0% by weight.

八l:^2は、Niと共存してN1Af相を析出し、時
効硬化に寄与する。そのためには0.4重量%以上の添
加が必要であるが、余り多過ぎると熱間加工性を阻害す
るので上限は1.5重量%とする。
8l:^2 coexists with Ni and precipitates the N1Af phase, contributing to age hardening. For this purpose, it is necessary to add 0.4% by weight or more, but if it is too large, hot workability will be inhibited, so the upper limit is set at 1.5% by weight.

更に、下記成分を添加しても本発明の効果を妨げない。Furthermore, even if the following components are added, the effects of the present invention will not be impaired.

S、 Pb、 Se、 Te、 Bi : S、 Pb
、 Se、 Ti、 Biは、いずれも被削性を向上さ
せる元素であり、そのためにはS≦0.3重量%、 p
b≦0.5重量%、 Se≦0.5重量%、 Te≦0
.5重量%、 Bi≦0.5重量%のうち、いずれか1
種または2種以上をそれぞれの量を上限として添加して
もよい。
S, Pb, Se, Te, Bi: S, Pb
, Se, Ti, and Bi are all elements that improve machinability, and for this purpose S≦0.3% by weight, p
b≦0.5% by weight, Se≦0.5% by weight, Te≦0
.. 5% by weight, any one of Bi≦0.5% by weight
A species or two or more species may be added in an amount of each species as an upper limit.

Ti+ L Nb+ Tan Zr : Ti、 L 
Nb+ Ta、 Zrなどの細粒化促進元素を靭性向上
のために添加してもよい。各添加元素は、Ti≦0.5
重量%、■≦0.5重量%、 Zr≦0.3重量%、 
Nb+Ta≦0.5重量%のうち一種以上を添加しても
よい。
Ti+ L Nb+ Tan Zr: Ti, L
Elements promoting grain refinement such as Nb+Ta and Zr may be added to improve toughness. Each additive element is Ti≦0.5
Weight%, ■≦0.5% by weight, Zr≦0.3% by weight,
One or more types of Nb+Ta≦0.5% by weight may be added.

Cr : Crは、耐食性を向上させるために必要な元
素であり、5.0重量%以下添加するとよい。
Cr: Cr is an element necessary to improve corrosion resistance, and is preferably added in an amount of 5.0% by weight or less.

前述した組成の鋼を加熱するに当っては、加熱温度を9
50″C〜1300″Cの範囲とする。即ち、950℃
未満では熱間加工であり、1300℃を超えるとスケー
ル生成または粒界溶融による熱間加工性の低下の恐れが
あるので、加熱温度範囲は950℃〜1300℃の範囲
とする。
When heating steel with the above-mentioned composition, the heating temperature should be set to 9.
The range is 50″C to 1300″C. That is, 950℃
If it is less than 1,300°C, it is hot working, and if it exceeds 1,300°C, there is a risk of deterioration in hot workability due to scale formation or grain boundary melting, so the heating temperature range is set in the range of 950°C to 1,300°C.

また、熱間加工温度が、700℃未満であると残留応力
が太き(歪が大きくなり、900 ’Cを超えると硬度
が低下し、機械的性質が劣化するので、熱間加工温度範
囲は700〜900℃の範囲とする。
In addition, if the hot working temperature is less than 700°C, residual stress (strain will increase), and if it exceeds 900°C, the hardness will decrease and the mechanical properties will deteriorate, so the hot working temperature range is The temperature should be in the range of 700 to 900°C.

次に、上記熱間加工温度における熱間加工率が10%未
満であると、ベイナイト変態を促進するための歪が不十
分であり、熱間加工率が40%を超えると鋼板の変形の
原因となるために、熱間加工率は10〜40%の範囲と
する。
Next, if the hot working rate at the above hot working temperature is less than 10%, the strain to promote bainite transformation will be insufficient, and if the hot working rate exceeds 40%, it will cause deformation of the steel plate. Therefore, the hot working rate is set in a range of 10 to 40%.

次に、時効処理時間は、1時間以上であれば充分である
が、100時間を超えると過時効となるので、1〜10
0時間とする。
Next, as for the aging treatment time, it is sufficient if it is 1 hour or more, but if it exceeds 100 hours, it will be overaged, so 1 to 10 hours or more is sufficient.
Let it be 0 hours.

(実施例) 第1表に示すC:0.12重置%、 St : 0.6
5重重量、Mn : 1.3重量%、Ni:2.11量
%、Mo : 0.25重量%、Cu : 1.1重量
%、Aj!:1.2重量%を含む鋼と、C: 0.07
重量%、Si : 0.41重量%、Mn : 1.5
重量%、Ni : 1.4重量%、Mo : 0.43
重量%、Cu:1.0重量%、Al:0.8重量%を含
む鋼を真空溶解後、1200”Cに加熱し、厚みが10
0 tmになるように予備圧延した。その後、第1図に
示すように、1200℃に1時間保持後、1050℃ま
でに50%圧延した後、第1表に示す各熱間圧延温度(
T、)で、同表中に示す各圧下率で熱間加工後、同表中
に示す温度(T2)で各保持時間、保持した後、冷却し
た。
(Example) C shown in Table 1: 0.12% overlapping, St: 0.6
5 weight, Mn: 1.3% by weight, Ni: 2.11% by weight, Mo: 0.25% by weight, Cu: 1.1% by weight, Aj! : Steel containing 1.2% by weight, C: 0.07
Weight %, Si: 0.41 weight %, Mn: 1.5
Weight%, Ni: 1.4% by weight, Mo: 0.43
After vacuum melting, steel containing Cu: 1.0 wt% and Al: 0.8 wt% was heated to 1200"C, and the thickness was 10% by weight.
Preliminary rolling was carried out so that it became 0 tm. Thereafter, as shown in Figure 1, after holding at 1200°C for 1 hour and rolling 50% to 1050°C, each hot rolling temperature shown in Table 1 (
After hot working at T, ) at each rolling reduction rate shown in the same table, the samples were held at the temperature (T2) shown in the same table for each holding time, and then cooled.

また、比較のために第1表に示す鋼を860℃に加熱し
て2時間保持後、30″C/分の冷却速度で冷却した後
、再度500℃に加熱し、3時間保持後、冷却した。(
第2図に示す。) 各熱処理により得られた材料の特性についての比較を第
2表に示す。同表からも判るように、本発明の製造条件
を満足するNαl−3及びN(L 10−12は、通常
の熱処理を経た処理材と比較して、同等の硬さとなると
共にベイナイトも多くなっている。
For comparison, the steel shown in Table 1 was heated to 860°C, held for 2 hours, cooled at a cooling rate of 30"C/min, heated again to 500°C, held for 3 hours, and then cooled. did.(
Shown in Figure 2. ) Table 2 shows a comparison of the properties of the materials obtained by each heat treatment. As can be seen from the same table, Nαl-3 and N(L 10-12, which satisfy the manufacturing conditions of the present invention, have the same hardness and more bainite than the treated materials that have undergone normal heat treatment. ing.

(発明の効果) 以上説明したように本発明によれば、ベイナイト相が多
くなるのでシボ加工性が改善され、また熱処理工程が短
縮されるので製品の納期も短縮される。
(Effects of the Invention) As explained above, according to the present invention, the amount of bainite phase is increased, so the texturing property is improved, and the heat treatment step is shortened, so the delivery time of the product is also shortened.

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

第1図は、本発明の熱処理パターンを示す一実施例であ
り、 第2図は、通常の熱処理パターンを示す図であり、 第38乃至第3d図は、熱間加工における各圧下率にお
ける圧延温度(T、)及び時効保持温度(T2)と、ベ
イナイト量及び硬さとの関係を示す図である。 第1図 hU工11ftWtY’l−7 第2図 (a) 600   9QQ    1000 丁1:圧延1度(’c) (圧下1!3%) 600    goo    1000η:圧延1虐(
’C) (圧1’$7%) 13図 (C) soo   Boo   wo。 丁1;圧延Jilt (’c) (圧7【樺ビ f3’をン 600    BOO1000 了−t :/1Jt−XI (”C) (圧F#2o%)
FIG. 1 is an example showing a heat treatment pattern of the present invention, FIG. 2 is a diagram showing a normal heat treatment pattern, and FIGS. It is a figure showing the relationship between temperature (T, ) and aging holding temperature (T2), and the amount of bainite and hardness. Figure 1 hU work 11ftWtY'l-7 Figure 2 (a) 600 9QQ 1000 1: Rolling 1 degree ('c) (Reduction 1!3%) 600 goo 1000η: Rolling 1 degree ('c)
'C) (Pressure 1'$7%) Figure 13 (C) soo boo wo. Rolling Jilt ('c) (pressure 7

Claims (1)

【特許請求の範囲】 1、C:0.05〜0.20重量%、 Si:0.1〜2.0重量%、 Mn:0.5〜2.1重量%、 Ni:0.5〜3.5重量%、 Mo:0.05〜0.6重量%、 Cu:0.5〜2.0重量%、 Al:0.4〜1.5重量%を含有する鋼を加熱し、熱
間圧延を経ず又は熱間圧延した後、700〜900℃の
温度範囲で10〜40%の加工を施し、その後450〜
550℃の温度範囲に1〜100時間保持した後、冷却
することを特徴とする析出硬化鋼の製造方法。
[Claims] 1. C: 0.05-0.20% by weight, Si: 0.1-2.0% by weight, Mn: 0.5-2.1% by weight, Ni: 0.5-0.5% by weight. 3.5% by weight, Mo: 0.05-0.6% by weight, Cu: 0.5-2.0% by weight, and Al: 0.4-1.5% by weight. After hot rolling or without inter-rolling, 10-40% processing is performed in a temperature range of 700-900°C, and then 450-400°C
A method for producing precipitation hardened steel, which comprises maintaining the temperature in a temperature range of 550°C for 1 to 100 hours, and then cooling.
JP30890786A 1986-12-26 1986-12-26 Manufacture of precipitation-hardening steel Pending JPS63162811A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP30890786A JPS63162811A (en) 1986-12-26 1986-12-26 Manufacture of precipitation-hardening steel

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP30890786A JPS63162811A (en) 1986-12-26 1986-12-26 Manufacture of precipitation-hardening steel

Publications (1)

Publication Number Publication Date
JPS63162811A true JPS63162811A (en) 1988-07-06

Family

ID=17986709

Family Applications (1)

Application Number Title Priority Date Filing Date
JP30890786A Pending JPS63162811A (en) 1986-12-26 1986-12-26 Manufacture of precipitation-hardening steel

Country Status (1)

Country Link
JP (1) JPS63162811A (en)

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02294449A (en) * 1989-04-24 1990-12-05 Boehler Gmbh Maraging steel
JPH04263041A (en) * 1991-02-15 1992-09-18 Nkk Corp High hardness steel for forming molds and its manufacturing method
JPH04263014A (en) * 1991-02-15 1992-09-18 Nkk Corp High hardness forming die steel and its production
JPH04263042A (en) * 1991-02-15 1992-09-18 Nkk Corp Steel for molding die having high hardness and its manufacture
JPH04263013A (en) * 1991-02-15 1992-09-18 Nkk Corp High hardness forming die steel and its production
JPH04263043A (en) * 1991-02-15 1992-09-18 Nkk Corp Steel for molding die having high hardness and its manufacture
JPH04263040A (en) * 1991-02-15 1992-09-18 Nkk Corp High hardness steel for forming molds and its manufacturing method
JP2007024260A (en) * 2005-07-20 2007-02-01 Ntn Corp Rolling member and roller bearing using the same

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH02294449A (en) * 1989-04-24 1990-12-05 Boehler Gmbh Maraging steel
JPH04263041A (en) * 1991-02-15 1992-09-18 Nkk Corp High hardness steel for forming molds and its manufacturing method
JPH04263014A (en) * 1991-02-15 1992-09-18 Nkk Corp High hardness forming die steel and its production
JPH04263042A (en) * 1991-02-15 1992-09-18 Nkk Corp Steel for molding die having high hardness and its manufacture
JPH04263013A (en) * 1991-02-15 1992-09-18 Nkk Corp High hardness forming die steel and its production
JPH04263043A (en) * 1991-02-15 1992-09-18 Nkk Corp Steel for molding die having high hardness and its manufacture
JPH04263040A (en) * 1991-02-15 1992-09-18 Nkk Corp High hardness steel for forming molds and its manufacturing method
JP2007024260A (en) * 2005-07-20 2007-02-01 Ntn Corp Rolling member and roller bearing using the same

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