JPH0314898B2 - - Google Patents

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Publication number
JPH0314898B2
JPH0314898B2 JP58044302A JP4430283A JPH0314898B2 JP H0314898 B2 JPH0314898 B2 JP H0314898B2 JP 58044302 A JP58044302 A JP 58044302A JP 4430283 A JP4430283 A JP 4430283A JP H0314898 B2 JPH0314898 B2 JP H0314898B2
Authority
JP
Japan
Prior art keywords
rolling
steel
strength
toughness
grain size
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.)
Expired - Lifetime
Application number
JP58044302A
Other languages
Japanese (ja)
Other versions
JPS59170241A (en
Inventor
Makoto Saito
Atsuyoshi Kimura
Yukio Ito
Kyoaki Nishigori
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.)
Daido Steel Co Ltd
Original Assignee
Daido Steel Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Daido Steel Co Ltd filed Critical Daido Steel Co Ltd
Priority to JP4430283A priority Critical patent/JPS59170241A/en
Publication of JPS59170241A publication Critical patent/JPS59170241A/en
Publication of JPH0314898B2 publication Critical patent/JPH0314898B2/ja
Granted legal-status Critical Current

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  • Heat Treatment Of Steel (AREA)

Description

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

本発明は、高強度でかつ高靭性を有し、疲労強
度が高く、特に自動車などの車両用懸架ばね素材
としての使用に適する高強度・高靭性ばね用鋼を
製造するのに利用される高強度・高靭性ばね用鋼
の製造方法に関するものである。 近年、自動車の走行性能や燃費を向上させるた
めに、その軽量化が進められており、自動車の構
成部品である懸架ばねにおいても軽量化が要求さ
れるようになつてきている。このような要求に対
し、ばね用鋼としては高応力化で対応することが
通常の考え方であり、その一つとして耐へたり性
を向上させたばね用鋼の開発がなされている。 従来、耐へたり性の優れたばね用鋼としては、
鋼中に含まれるSiが耐へたり性に有効な元素であ
ることから、JIS SUP6およびこれよりもSi含有
量が多いSUP7が使用されてきた。そして、最近
ではSUP7よりもさらに耐へたり性の優れたばね
用鋼の開発が進められ、一部ではSUP6、SUP7
にNb、Vなどを添加した鋼が使用されている。 本発明者らはこのような要求に対応すべく鋭意
研究を進め、耐へたり性だけではなく疲労強度を
著しく高めた高強度・高靭性ばね用鋼を得ること
を目的としてその製造方法について詳細に研究を
行つた結果、C、Si、Mn、Crを特定量組合わせ
て含有させ、これにAl、V、Nbの1種以上を添
加し、使用目的に応じてさらにBを添加し、さら
には疲労強度をより一層改善するために[S]お
よび[O]含有量を規制し、さらにはこのような
特定成分の鋼に対して特定の圧延条件を選択して
圧延を行つて鋼の結晶粒度を9番とすることによ
り、上記目的を達成することができることを見い
出した。 すなわち、本発明による特許請求の範囲第1項
に記載された高強度・高靭性ばね用鋼の製造方法
は、重量%で、C:0.40〜0.75%、Si:1.0〜2.5
%、Mn:0.5〜1.0%、Cr:0.1〜1.0%、および
Al:0.01〜0.1%、V:0.03〜0.3%、Nb:0.01〜
0.3%の1種または2種以上を含有し、残部Feお
よび不純物からなる鋼を930〜980℃に加熱して熱
間圧延を行い、仕上圧延温度を900℃以下にする
と共に仕上圧延での圧下率を5%以上にし、圧延
後Ar1変態点までの冷却速度を30℃/min以上と
することにより結晶粒度が9番以上である高強
度・高靭性ばね用鋼を得る構成としたことを特徴
としており、また本発明による特許請求の範囲第
2項に記載された高強度・高靭性ばね用鋼の製造
方法は、重量%で、C:0.40〜0.75%、Si:1.0〜
2.5%、Mn:0.5〜1.0%、Cr:0.1〜1.0%、および
Al:0.01〜0.1%、V:0.03〜0.3%、Nb:0.01〜
0.3%の1種または2種以上を含有し、さらに
[S]≦0.010%、[O]≦0.0015%に規制し、残部
Feおよび不純物からなる鋼を930〜980℃に加熱
して熱間圧延を行い、仕上圧延温度を900℃以下
にすると共に仕上圧延での圧下率を5%以上に
し、圧延後Ar1変態点までの冷却速度を30℃/
min以上とすることにより結晶粒度が9番以上で
ある高強度・高靭性ばね用鋼を得る構成としたこ
とを特徴としており、さらに、本発明による特許
請求の範囲第3項に記載された高強度・高靭性ば
ね用鋼の製造方法は、重量%で、C:0.40〜0.75
%、Si:1.0〜2.5%、Mn:0.5〜1.0%、Cr:0.1〜
1.0%、およびAl:0.01〜0.1%、V:0.03〜0.3%、
Nb:0.01〜0.3%の1種または2種以上を含有し、
さらにB:0.0005〜0.01%を含み、残部Feおよび
不純物からなる鋼を930〜980℃に加熱して熱間圧
延を行い、仕上圧延温度を900℃以下にすると共
に仕上圧延での圧下率を5%以上にし、圧延後
Ar1変態点までの冷却速度を30℃/min以上とす
ることにより結晶粒度が9番以上である高強度・
高靭性ばね用鋼を得る構成としたことを特徴とし
ており、さらにまた、本発明による特許請求の範
囲第4項に記載された高強度・高靭性ばね用鋼の
製造方法は、重量%で、C:0.40〜0.75%、Si:
1.0〜2.5%、Mn:0.5〜1.0%、Cr:0.1〜1.0%、
およびAl:0.01〜0.1%、V:0.03〜0.3%、Nb:
0.01〜0.3%の1種または2種以上を含有し、さ
らにB:0.0005〜0.01%を含み、[S]≦0.010%、
[O]≦0.0015%に規制し、残部Feおよび不純物か
らなる鋼を930〜980℃に加熱して熱間圧延を行
い、仕上圧延温度を900℃以下にすると共に仕上
圧延での圧下率を5%以上にし、圧延後Ar1変態
点までの冷却速度を30℃/min以上とすることに
より結晶粒度が9番以上である高強度・高靭性ば
ね用鋼を得る構成としたことを特徴としている。 次に、本発明による高強度・高靭性ばね用鋼の
製造方法において適用される鋼の成分範囲(重量
%)および当該鋼に対する圧延条件の限定理由を
説明する。 C(炭素): Cは、鋼の強度を高めるのに有効な元素である
が、0.40%未満ではばねとしての必要な強度を得
ることができず、0.75%を超えると鋼状のセメン
タイトが出やすくなり、ばねの疲労強度が損われ
るので、0.40〜0.75%の範囲とした。 Si(けい素); Siは、鋼の強度を向上し、ばねの耐へたり性を
向上させるのに有効な元素であるが、1.0%未満
ではばねとして必要な耐へたり性を得ることがで
きず、2.5%を超えると靭性が劣化するので、1.0
〜2.5%の範囲とした。 Mn(マンガン); Mnは、鋼の脱酸に有効であると共にSによる
害を阻止するのに有効な元素であり、このために
は0.5%以上含有させることが必要であるが、1.0
%を超えると焼入性が過大になつて靭性を劣化す
ると共に焼入れ時の変形の原因となりやすいの
で、0.5〜1.0%の範囲とした。 Cr(クロム); Crは、高炭素鋼の脱炭および黒鉛化を防止す
るのに有効な元素であるが、0.1%未満ではこれ
らの効果を十分に期待することができず、1.0%
を超えると靭性が劣化するので、0.1〜1.0%の範
囲とした。 Al(アルミニウム)、V(バナジウム)、Nb(ニオ
ブ); Al、V、Nbは、低温圧延時の結晶粒微細化効
果が大きく、ばね特性の向上および信頼性の増大
を得ることができ、また、V、Nbは焼入れ焼も
どし時の析出硬化にも寄与する。そして、Alに
ついては、0.01%未満では結晶粒微細化の効果が
小さく、0.1%を超えると地疵発生の原因となる
ので、0.01〜0.1%の範囲とした。また、Vにつ
いては、0.03%未満では上記した結晶粒微細化お
よび析出硬化の効果があまり期待できず、0.3%
を超えると製鋼上の取扱いが困難となるので、
0.03〜0.3%の範囲とした。さらに、Nb(Nb+Ta
でも可)については、0.01%未満では結晶粒微細
化および析出硬化の効果があまり期待できず、ま
た焼入加熱時の結晶粒粗大化をおさえる効果が十
分得られず、0.3%を超えると造塊時に炭化物
(NbC)がストリンガー状に生成し、これが通常
の分塊圧延時に溶体化せず、また後の熱処理で溶
解しにくく、製品としてのばね特性を低下させる
ので、0.01〜0.3%の範囲とした。 B(ボロン); Bは、鋼の焼入性を増大させるのに有効な元素
であり、必要なばね特性が得られるように使用目
的等に応じて添加するが、0.0005%未満では上記
した効果が得られず、0.01%を超えても上記した
効果は増大しないので、0.0005〜0.01%の範囲と
した。 [S](いおう): Sは、ばねの疲労強度を損う元素であり、S含
有量が低いほどばねとしての信頼性を高めること
ができるので、使用目的等に応じてその上限を規
制するのが良い。そして、0.010%以下であれば
Sによる害はほとんどなくなるので、0.010%以
下とした。 [O](酸素): Oは酸化物系の介在物を生成し、これが疲労破
壊の起点となりやすいので、使用目的等に応じて
その含有量を規制するのが良く、この場合、
0.0015%以下であれば、疲労破壊の起点となりに
くいので、0.0015%以下とした。 圧延条件; このような成分含有量の鋼を素材とするばねに
おいて、その耐へたり性および疲労強度をさらに
向上させるように、特定の圧延条件を選定するこ
とによつて結晶粒度を9番以上とする。ここで、
特定の圧延条件を選定することにより結晶粒度を
9番以上となるようにしたのは、結晶粒度が9番
未満では十分な耐へたり性および疲労強度が得ら
れないためであり、結晶粒度が同じ9番以上であ
つても、以下に示す特定の圧延条件によつて9番
以上としたものは耐へたり性および疲労強度がさ
らに向上するためである。 本発明において選定した圧延条件は、上記にお
いて示した特定の鋼に対する加熱温度を930〜980
℃、仕上圧延温度を900℃以下、仕上圧延での圧
下率を5%以、圧延後Ar1変態点までの冷却速度
を30℃/min以上としている。 加熱温度;930〜980℃ 従来、Si含有量が1.0%以上である高Si鋼にお
いては、加熱温度を1000℃以上としている。これ
は、高Si鋼は低温加熱領域において元来脱炭を生
じやすい(α領域が広い)うえに、スケール(酸
化物)の生成速度が脱炭速度を上回り、さらには
脱炭の生じやすいα+γ領域を徐冷する結果とし
て大きな脱炭層が形成され、ばねの耐へたり性を
大きく低下させてしまうのを防止するためであ
る。また、NbやVを添加した鋼においても従来
の場合には脱炭の懸念があるとして1000℃以の加
熱温度を採用するようにしていた。これはまた、
高温加熱によりいつたん固溶したNbやVが圧延
過程においてNbCやVCあるいはこれらの複合化
合物として析出し、この析出効果によつてそれな
りに耐へたり性向上の効果が得られることにもよ
つている。 このような従来の技術に対して、本発明におい
てはビレツトなどの圧延素材において析出した
NbCやVCが素材加熱時に脱炭の抵抗となること
を見い出した。また、このような炭化物が結晶粒
の粗大化を防止するのに寄与することもわかつ
た。 したがつて、本発明においては従来の加熱温度
よりも低い温度にすることを可能にしたものであ
り、加熱温度が930℃よりも低いとばね用鋼が高
炭素鋼であることも影響して圧延時の負荷が増大
して圧延効率が低下したりロールの折損をきたし
たりするおそれがあるためであり、980℃よりも
高いとNbやVの炭化物が一部基地中に溶け込ん
でビレツト加熱時の初期結晶粒が粗大化するおそ
れがあるためである。 仕上圧延温度;900℃以下、仕上圧延での圧下
率;5%以上 最終圧延ロールでの圧延温度および圧下率に関
し、熱間圧延後の再結晶および再結晶粒の成長を
効果的におさえるようにするためには、仕上圧延
温度を900℃以下、仕上圧延での圧下率を5%以
上とするのが有効であるので、このような仕上圧
延条件を設定した。 圧延後Ar1変態点までの冷却速度:30℃/min
以上 圧延後Ar1変態点までの冷却速度は、これが遅
すぎると再結晶をおさえることができないととも
に、使用にとつて有害な脱炭層が残存するように
なるので、圧延後の再結晶をおさえるためおよび
脱炭を防止するために、30℃/min以上とするこ
とが必要である。 次に本発明の実施例を比較例とともに説明す
る。 次表に示す化学成分の鋼を溶製したのち鋳造し
分塊圧延してビレツトを作成した。次いで、ビレ
ツト加熱温度を同表に示す値にして圧延を開始
し、最終圧延ロールにより同表に示す仕上圧延温
度および圧下で圧延を行い、仕上圧延後Ar1変態
点までを同表に示す冷却速度で冷却してばね用鋼
線を製造した。その後、各ばね用鋼線の結晶粒度
をJISの規定に準じて測定したところ、同じく表
に示す結果が得られた。 次に、各ばね用鋼線の静的へたりおよび疲労強
度を測定した。このとき、静的へたりは、へたり
時応力が180Kgf/mm2であるように調質したばね
常数3のコイルばねを120Kgfの荷重でセツテイ
ングし、110Kgfの荷重で150時間加圧した後の静
的へたり(残留剪断歪)で測定した。その結果を
同じく表に示す。一方、疲労強度は、各ばね用鋼
線の硬さがHRC45〜48となるように調質し、小野
式回転曲げ疲労試験機により測定した。この結果
を同じく表に示す。
The present invention has high strength, high toughness, and high fatigue strength, and is particularly suitable for use as a suspension spring material for vehicles such as automobiles. The present invention relates to a method for producing high-strength, high-toughness spring steel. In recent years, in order to improve the driving performance and fuel efficiency of automobiles, efforts have been made to reduce the weight of automobiles, and suspension springs, which are component parts of automobiles, are also required to be reduced in weight. It is a common idea to meet such demands by increasing the stress of spring steels, and one of the ways to do this is to develop spring steels with improved fatigue resistance. Traditionally, spring steels with excellent resistance to fatigue include:
JIS SUP6 and SUP7, which has a higher Si content, have been used because Si contained in steel is an effective element for resistance to fatigue. Recently, the development of spring steels that are even more resistant to fatigue than SUP7 has progressed, and in some cases SUP6, SUP7
Steel to which Nb, V, etc. are added is used. In order to meet these demands, the present inventors have carried out extensive research and have detailed the manufacturing method with the aim of obtaining a high-strength, high-toughness spring steel with significantly improved fatigue strength as well as fatigue resistance. As a result of our research, we found that by containing a specific amount of C, Si, Mn, and Cr in combination, adding one or more of Al, V, and Nb, and further adding B depending on the purpose of use. In order to further improve the fatigue strength, [S] and [O] contents are regulated, and specific rolling conditions are selected for steel with such specific components to improve the crystallization of the steel. It has been found that the above objective can be achieved by setting the particle size to No. 9. That is, the method for manufacturing a high-strength, high-toughness spring steel according to claim 1 of the present invention includes C: 0.40 to 0.75% and Si: 1.0 to 2.5% by weight.
%, Mn: 0.5-1.0%, Cr: 0.1-1.0%, and
Al: 0.01~0.1%, V: 0.03~0.3%, Nb: 0.01~
Steel containing 0.3% of one or more of the above, with the balance consisting of Fe and impurities is heated to 930-980°C and hot-rolled, and the finish rolling temperature is reduced to 900°C or less and the rolling is performed in the finish rolling. By setting the ratio to 5% or more and the cooling rate to the Ar 1 transformation point after rolling to 30°C/min or more, a high-strength and high-toughness spring steel with a grain size of No. 9 or more can be obtained. The method for producing high-strength and high-toughness spring steel according to the present invention, which is characterized by the following claim 2, is characterized in that, in weight percent, C: 0.40 to 0.75%, Si: 1.0 to
2.5%, Mn: 0.5~1.0%, Cr: 0.1~1.0%, and
Al: 0.01~0.1%, V: 0.03~0.3%, Nb: 0.01~
Contains one or more of 0.3% of
Steel consisting of Fe and impurities is heated to 930-980°C and hot rolled, the finish rolling temperature is set to 900°C or less, the rolling reduction in finish rolling is set to 5% or more, and the temperature is reduced to Ar 1 transformation point after rolling. cooling rate of 30℃/
min or more to obtain a high-strength, high-toughness spring steel having a crystal grain size of No. 9 or more, and furthermore, the high The manufacturing method for high-strength/high-toughness spring steel is C: 0.40 to 0.75 in weight%.
%, Si: 1.0~2.5%, Mn: 0.5~1.0%, Cr: 0.1~
1.0%, and Al: 0.01-0.1%, V: 0.03-0.3%,
Nb: Contains 0.01 to 0.3% of one or more types,
Further, the steel containing 0.0005 to 0.01% of B, with the remainder Fe and impurities, is heated to 930 to 980°C and hot rolled, and the finish rolling temperature is set to 900°C or less, and the rolling reduction in the finish rolling is reduced to 5. % or more and after rolling
By setting the cooling rate to the Ar 1 transformation point at 30°C/min or more, the crystal grain size is 9 or more.
It is characterized by having a configuration for obtaining a high-toughness steel for springs, and furthermore, the method for producing high-strength and high-toughness steel for springs according to claim 4 of the present invention has the following features: C: 0.40-0.75%, Si:
1.0~2.5%, Mn: 0.5~1.0%, Cr: 0.1~1.0%,
and Al: 0.01-0.1%, V: 0.03-0.3%, Nb:
Contains one or more of 0.01 to 0.3%, further contains B: 0.0005 to 0.01%, [S]≦0.010%,
[O] is regulated to 0.0015%, and the steel consisting of the balance Fe and impurities is heated to 930 to 980°C and hot rolled, the finish rolling temperature is set to 900°C or less, and the rolling reduction in the finish rolling is set to 5%. % or more and the cooling rate to the Ar 1 transformation point after rolling is 30°C/min or more to obtain a high-strength, high-toughness spring steel with a grain size of No. 9 or more. . Next, the reason for limiting the range of steel components (weight %) and rolling conditions for the steel applied in the method for manufacturing high-strength, high-toughness spring steel according to the present invention will be explained. C (carbon): C is an effective element for increasing the strength of steel, but if it is less than 0.40%, it will not be possible to obtain the strength necessary for a spring, and if it exceeds 0.75%, steel-like cementite will be produced. Since the fatigue strength of the spring is impaired, it is set in the range of 0.40 to 0.75%. Si (silicon): Si is an effective element for improving the strength of steel and the fatigue resistance of springs, but if it is less than 1.0%, it may not be possible to obtain the fatigue resistance required for springs. If it exceeds 2.5%, the toughness will deteriorate, so 1.0
The range was set at ~2.5%. Mn (manganese): Mn is an element that is effective in deoxidizing steel as well as preventing damage caused by S. For this purpose, it is necessary to contain 0.5% or more, but 1.0
If it exceeds 0.5%, the hardenability becomes excessive, degrading the toughness and easily causing deformation during quenching. Cr (chromium): Cr is an element effective in preventing decarburization and graphitization of high carbon steel, but if it is less than 0.1%, these effects cannot be fully expected;
Since toughness deteriorates when the content exceeds 0.1% to 1.0%. Al (aluminum), V (vanadium), Nb (niobium); Al, V, and Nb have a large grain refinement effect during low-temperature rolling, and can improve spring characteristics and reliability. , V, and Nb also contribute to precipitation hardening during quenching and tempering. Regarding Al, if it is less than 0.01%, the effect of grain refinement will be small, and if it exceeds 0.1%, it will cause scratches, so it was set in the range of 0.01 to 0.1%. Regarding V, if it is less than 0.03%, the effects of grain refinement and precipitation hardening described above cannot be expected;
If it exceeds, it becomes difficult to handle in steel manufacturing.
The range was 0.03% to 0.3%. Furthermore, Nb (Nb+Ta
If it is less than 0.01%, the effect of crystal grain refinement and precipitation hardening cannot be expected, and the effect of suppressing crystal grain coarsening during quenching heating cannot be sufficiently obtained, and if it exceeds 0.3%, Carbide (NbC) is formed in the form of stringers during lumping, and this does not become a solution during normal blooming and is difficult to dissolve during subsequent heat treatment, reducing the spring properties of the product, so the range is 0.01 to 0.3%. And so. B (Boron): B is an effective element for increasing the hardenability of steel, and is added depending on the purpose of use to obtain the necessary spring characteristics, but if it is less than 0.0005%, it will not have the above effects. is not obtained, and the above-mentioned effects do not increase even if the content exceeds 0.01%, so the content was set in the range of 0.0005 to 0.01%. [S] (sulfur): S is an element that impairs the fatigue strength of springs, and the lower the S content, the more reliable the spring will be, so its upper limit is regulated depending on the purpose of use, etc. It's good. If it is 0.010% or less, there will be almost no harm caused by S, so it was set at 0.010% or less. [O] (Oxygen): O generates oxide-based inclusions, which tend to become the starting point of fatigue failure, so it is best to regulate its content depending on the purpose of use, etc. In this case,
If it is 0.0015% or less, it is unlikely to become a starting point for fatigue fracture, so it is set to 0.0015% or less. Rolling conditions: In order to further improve the fatigue resistance and fatigue strength of springs made of steel with such component contents, by selecting specific rolling conditions, the grain size can be increased to No. 9 or higher. shall be. here,
The reason why the grain size was made to be No. 9 or higher by selecting specific rolling conditions was because if the grain size was less than No. 9, sufficient fatigue resistance and fatigue strength could not be obtained. This is because even if the number is 9 or higher, if the number is 9 or higher depending on the specific rolling conditions shown below, the sag resistance and fatigue strength are further improved. The rolling conditions selected in the present invention include heating temperatures of 930 to 980 for the specific steel shown above.
℃, the finish rolling temperature is 900℃ or less, the reduction rate in finish rolling is 5% or more, and the cooling rate after rolling to the Ar 1 transformation point is 30℃/min or more. Heating temperature: 930 to 980°C Conventionally, in high-Si steel with a Si content of 1.0% or more, the heating temperature is set to 1000°C or more. This is because high-Si steel is inherently prone to decarburization in the low-temperature heating region (the α region is wide), and the rate of scale (oxide) formation exceeds the decarburization rate, making it more likely that decarburization will occur (α + γ). This is to prevent a large decarburized layer from being formed as a result of slowly cooling the region, which would greatly reduce the fatigue resistance of the spring. Furthermore, even for steels containing Nb or V, heating temperatures of 1000°C or higher have traditionally been adopted due to concerns about decarburization. This is also
This is because Nb and V, which have been dissolved in solid solution due to high-temperature heating, precipitate as NbC, VC, or a composite compound of these during the rolling process, and this precipitation effect can improve the resistance to settling to a certain extent. There is. In contrast to such conventional techniques, in the present invention, the precipitated material in rolled materials such as billets can be
We found that NbC and VC act as resistance to decarburization when heating the material. It was also found that such carbides contribute to preventing coarsening of crystal grains. Therefore, in the present invention, it is possible to lower the heating temperature than the conventional heating temperature, and if the heating temperature is lower than 930°C, the fact that the spring steel is high carbon steel also affects the heating temperature. This is because the load during rolling increases, which may reduce rolling efficiency or breakage of the rolls. If the temperature is higher than 980°C, some Nb and V carbides will melt into the matrix and cause problems during billet heating. This is because the initial crystal grains may become coarse. Finish rolling temperature: 900℃ or less, Reduction rate in finish rolling: 5% or more The rolling temperature and reduction rate in the final rolling roll are set to effectively suppress recrystallization and growth of recrystallized grains after hot rolling. In order to achieve this, it is effective to set the finish rolling temperature to 900° C. or less and the rolling reduction in finish rolling to 5% or more, so these finish rolling conditions were set. Cooling rate to Ar 1 transformation point after rolling: 30℃/min
The cooling rate to the Ar 1 transformation point after rolling should be set to suppress recrystallization after rolling, because if it is too slow, it will not be possible to suppress recrystallization, and a decarburized layer will remain that is harmful to use. In order to prevent decarburization, it is necessary to set the temperature at 30°C/min or higher. Next, examples of the present invention will be described together with comparative examples. Steel with the chemical composition shown in the table below was melted, cast, and bloomed to form billets. Next, rolling was started with the billet heating temperature set to the value shown in the same table, and rolling was carried out using the final rolling roll at the finish rolling temperature and rolling pressure shown in the same table. After finishing rolling, the billet was cooled to the Ar 1 transformation point shown in the table. A steel wire for springs was manufactured by cooling at a high speed. Thereafter, the grain size of each spring steel wire was measured according to JIS regulations, and the same results shown in the table were obtained. Next, the static fatigue and fatigue strength of each spring steel wire were measured. At this time, the static settiness is determined by setting a coil spring with a spring constant of 3 that has been tempered so that the stress at sett is 180Kgf/mm 2 under a load of 120Kgf, and pressurizing it with a load of 110Kgf for 150 hours. Measured by static settling (residual shear strain). The results are also shown in the table. On the other hand, the fatigue strength was measured using an Ono rotary bending fatigue tester after tempering each spring steel wire to have a hardness of H R C45 to 48. The results are also shown in the table.

【表】【table】

【表】 表に示す結果より明らかなように、本発明で特
定した圧延条件を満足せず、結晶粒度が9番以下
である試料No.1〜7のものでは、いずれも残留剪
断歪が大きく、疲労強度が低いことがわかる。こ
れに対して、本発明で特定した圧延条件による圧
延を行い、結晶粒度が9番以上である試料No.8〜
32では、いずれも残留剪断歪が小さく、疲労強度
も高いことがわかる。そして、とくに〔S〕、
〔O〕含有量をそれぞれ0.010%以下、0.0015%以
下に規制した本発明の試料No.15〜20および試料No.
27〜32のものでは、疲労強度がさらに高くなつて
いた。また、Bを添加した場合にも疲労強度を高
めることができ、とくに線径の太いばねの性能お
よび信頼性を高めることができた。そして、脱炭
層の深さはいずれも0.05mm程度であつた。 一方、添付図面は、試料No.1、7について結晶
粒度の変化による疲労強度の変化を示したもので
あつて、熱処理のみによつては結晶粒度の調整は
せいぜい10までが限度であり、疲労強度も低いも
のである。これに対して制御圧延した場合には結
晶粒度の調製は12位までも可能であり、また疲労
強度もかなり高めることができた。そして、同じ
結晶粒度であつても制御圧延をした場合としない
場合とでは疲労強度にかなり差を生ずることが確
認された。 以上説明してきたように、本発明による高強
度・高靭性ばね用鋼の製造方法では、C、Si、
Mn、Crを特定量組合わせて含有させ、これに
Al、V、Nbの1種以上を添加し、使用目的に応
じてさらにBを添加し、疲労強度をより一層改善
するために使用目的に応じて[S]および[O]
含有量を規制し、さらにはこのような特定成分の
鋼に対して特定の圧延条件を選択して圧延を行う
ことにより鋼の結晶粒度を9番以上としたから、
耐へたり性だけでなく疲労強度を著しく高めた高
強度・高靭性ばね用鋼が得られ、車両用懸架ばね
素材として使用した場合の軽量化を実現すること
ができるという優れた効果を有する。
[Table] As is clear from the results shown in the table, all samples Nos. 1 to 7, which did not satisfy the rolling conditions specified in the present invention and had a grain size of 9 or less, had large residual shear strains. , it can be seen that the fatigue strength is low. On the other hand, samples No.8 to
32, it can be seen that the residual shear strain is small and the fatigue strength is high. And especially [S],
Sample Nos. 15 to 20 and Sample No. 2 of the present invention whose [O] content was regulated to 0.010% or less and 0.0015% or less, respectively.
Those with numbers 27 to 32 had even higher fatigue strength. Furthermore, when B was added, the fatigue strength could be increased, and in particular, the performance and reliability of springs with large wire diameters could be improved. The depth of the decarburized layer was approximately 0.05 mm in all cases. On the other hand, the attached drawings show changes in fatigue strength due to changes in grain size for Samples Nos. 1 and 7, and show that by heat treatment alone, the grain size can only be adjusted to 10 at most, and fatigue The strength is also low. On the other hand, when controlled rolling was carried out, it was possible to adjust the grain size to as low as 12, and it was also possible to considerably increase the fatigue strength. It was also confirmed that even if the grain size is the same, there is a considerable difference in fatigue strength between controlled rolling and non-controlled rolling. As explained above, in the method for producing high-strength and high-toughness spring steel according to the present invention, C, Si,
Contains a specific amount of Mn and Cr in combination, and
One or more of Al, V, and Nb are added, and B is further added depending on the purpose of use, and [S] and [O] are added according to the purpose of use to further improve fatigue strength.
By regulating the content and further selecting specific rolling conditions for steel with such specific components, the grain size of the steel was made to be No. 9 or higher.
A high-strength, high-toughness spring steel with significantly improved fatigue strength as well as fatigue resistance is obtained, and has the excellent effect of reducing weight when used as a suspension spring material for vehicles.

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

添付図面は、結晶粒度の変化による疲労強度の
変化を制御圧延の有無とともに調べた結果の一例
を示すグラフである。
The attached drawing is a graph showing an example of the results of examining changes in fatigue strength due to changes in grain size, together with the presence or absence of controlled rolling.

Claims (1)

【特許請求の範囲】 1 重量%で、C:0.40〜0.75%、Si:1.0〜2.5
%、Mn:0.5〜1.0%、Cr:0.1〜1.0%、および
Al:0.01〜0.1%、V:0.03〜0.3%、Nb:0.01〜
0.3%の1種または2種以上を含有し、残部Feお
よび不純物からなる鋼を930〜980℃に加熱して熱
間圧延を行い、仕上圧延温度を900℃以下にする
と共に仕上圧延での圧下率を5%以上にし、圧延
後Ar1変態点までの冷却速度を30℃/min以上と
することにより結晶粒度が9番以上である高強
度・高靭性ばね用鋼を得ることを特徴とする高強
度・高靭性ばね用鋼の製造方法。 2 重量%で、C:0.40〜0.75%、Si:1.0〜2.5
%、Mn:0.5〜1.0%、Cr:0.1〜1.0%、および
Al:0.01〜0.1%、V:0.03〜0.3%、Nb:0.01〜
0.3%の1種または2種以上を含有し、さらに
[S]≦0.010%、[O]≦0.0015%に規制し、残部
Feおよび不純物からなる鋼を930〜980℃に加熱
して熱間圧延を行い、仕上圧延温度を900℃以下
にすると共に仕上圧延での圧下率を5%以上に
し、圧延後Ar1変態点までの冷却速度を30℃/
min以上とすることにより結晶粒度が9番以上で
ある高強度・高靭性ばね用鋼を得ることを特徴と
する高強度・高靭性ばね用鋼の製造方法。 3 重量%で、C:0.40〜0.75%、Si:1.0〜2.5
%、Mn:0.5〜1.0%、Cr:0.1〜1.0%、および
Al:0.01〜0.1%、V:0.03〜0.3%、Nb:0.01〜
0.3%の1種または2種以上を含有し、さらに
B:0.0005〜0.01%を含み、残部Feおよび不純物
からなる鋼を930〜980℃に加熱して熱間圧延を行
い、仕上圧延温度を900℃以下にすると共に仕上
圧延での圧下率を5%以上にし、圧延後Ar1変態
点までの冷却速度を30℃/min以上とすることに
より結晶粒度が9番以上である高強度・高靭性ば
ね用鋼を得ることを特徴とする高強度・高靭性ば
ね用鋼の製造方法。 4 重量%で、C:0.40〜0.75%、Si:1.0〜2.5
%、Mn:0.5〜1.0%、Cr:0.1〜1.0%、および
Al:0.01〜0.1%、V:0.03〜0.3%、Nb:0.01〜
0.3%の1種または2種以上を含有し、さらに
B:0.0005〜0.01%を含み、[S]≦0.010%、[O]
≦0.0015%に規制し、残部Feおよび不純物からな
る鋼を930〜980℃に加熱して熱間圧延を行い、仕
上圧延温度を900℃以下にすると共に仕上圧延で
の圧下率を5%以上にし、圧延後Ar1変態点まで
の冷却速度を30℃/min以上とすることにより結
晶粒度が9番以上である高強度・高靭性ばね用鋼
を得ることを特徴とする高強度・高靭性ばね用鋼
の製造方法。
[Claims] 1% by weight, C: 0.40-0.75%, Si: 1.0-2.5
%, Mn: 0.5-1.0%, Cr: 0.1-1.0%, and
Al: 0.01~0.1%, V: 0.03~0.3%, Nb: 0.01~
Steel containing 0.3% of one or more of the above, with the balance consisting of Fe and impurities is heated to 930-980°C and hot-rolled, and the finish rolling temperature is reduced to 900°C or less and the rolling is performed in the finish rolling. It is characterized by obtaining a high-strength, high-toughness spring steel with a grain size of No. 9 or more by setting the rolling ratio to 5% or more and cooling rate to the Ar 1 transformation point after rolling to 30°C/min or more. A method for manufacturing high-strength, high-toughness spring steel. 2 Weight%: C: 0.40-0.75%, Si: 1.0-2.5
%, Mn: 0.5-1.0%, Cr: 0.1-1.0%, and
Al: 0.01~0.1%, V: 0.03~0.3%, Nb: 0.01~
Contains one or more of 0.3% of
Steel consisting of Fe and impurities is heated to 930-980°C and hot rolled, the finish rolling temperature is set to 900°C or less, the rolling reduction in finish rolling is set to 5% or more, and the temperature is reduced to Ar 1 transformation point after rolling. cooling rate of 30℃/
A method for producing a high-strength, high-toughness spring steel, characterized in that a high-strength, high-toughness spring steel having a crystal grain size of No. 9 or higher is obtained by adjusting the grain size to be at least min. 3 In weight%, C: 0.40-0.75%, Si: 1.0-2.5
%, Mn: 0.5-1.0%, Cr: 0.1-1.0%, and
Al: 0.01~0.1%, V: 0.03~0.3%, Nb: 0.01~
A steel containing 0.3% of one or two or more kinds, further containing 0.0005 to 0.01% of B, and the balance consisting of Fe and impurities is heated to 930 to 980°C and hot rolled, and the finish rolling temperature is set to 900°C. ℃ or less, the rolling reduction in finish rolling is 5% or more, and the cooling rate to the Ar 1 transformation point after rolling is 30℃/min or more, resulting in high strength and toughness with a grain size of No. 9 or more. A method for producing high-strength and high-toughness spring steel, characterized by obtaining spring steel. 4 In weight%, C: 0.40-0.75%, Si: 1.0-2.5
%, Mn: 0.5-1.0%, Cr: 0.1-1.0%, and
Al: 0.01~0.1%, V: 0.03~0.3%, Nb: 0.01~
Contains 0.3% of one or more types, further contains B: 0.0005 to 0.01%, [S]≦0.010%, [O]
≦0.0015%, and the remaining Fe and impurity steel is heated to 930 to 980°C and hot rolled, the finish rolling temperature is 900°C or less, and the rolling reduction in finish rolling is 5% or more. A high-strength, high-toughness spring characterized by obtaining a high-strength, high-toughness spring steel having a grain size of No. 9 or higher by cooling the cooling rate to the Ar 1 transformation point after rolling at 30°C/min or higher. Manufacturing method for industrial steel.
JP4430283A 1983-03-18 1983-03-18 Steel for high-strength and high-toughness spring Granted JPS59170241A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4430283A JPS59170241A (en) 1983-03-18 1983-03-18 Steel for high-strength and high-toughness spring

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4430283A JPS59170241A (en) 1983-03-18 1983-03-18 Steel for high-strength and high-toughness spring

Publications (2)

Publication Number Publication Date
JPS59170241A JPS59170241A (en) 1984-09-26
JPH0314898B2 true JPH0314898B2 (en) 1991-02-27

Family

ID=12687701

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4430283A Granted JPS59170241A (en) 1983-03-18 1983-03-18 Steel for high-strength and high-toughness spring

Country Status (1)

Country Link
JP (1) JPS59170241A (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62170460A (en) * 1986-01-21 1987-07-27 Honda Motor Co Ltd High strength valve spring steel and its manufacture
JP2650225B2 (en) * 1986-01-30 1997-09-03 大同特殊鋼株式会社 Spring steel
JP2619864B2 (en) * 1986-12-09 1997-06-11 日本発条株式会社 Spring steel
JP2860789B2 (en) * 1987-04-30 1999-02-24 愛知製鋼 株式会社 Spring steel with excellent hardenability and durability
JP2613601B2 (en) * 1987-09-25 1997-05-28 日産自動車株式会社 High strength spring
JP2839900B2 (en) * 1989-05-29 1998-12-16 愛知製鋼株式会社 Spring steel with excellent durability and sag resistance
US5258082A (en) * 1991-11-18 1993-11-02 Nhk Spring Co., Ltd. High strength spring
KR100398387B1 (en) * 1998-12-22 2003-12-18 주식회사 포스코 A method of manufacturing high strength wire rods having superior fatigue life for engine valve-spring

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5925024B2 (en) * 1980-06-26 1984-06-13 株式会社神戸製鋼所 steel for suspension springs
JPS6041699B2 (en) * 1981-05-16 1985-09-18 愛知製鋼株式会社 Spring steel with excellent hardenability and fatigue resistance
JPS5827956A (en) * 1981-08-11 1983-02-18 Aichi Steel Works Ltd Spring steel with superior wear resistance
JPS5827759A (en) * 1981-08-12 1983-02-18 Toshiba Corp Metallic painting method
JPS5842754A (en) * 1981-09-04 1983-03-12 Kobe Steel Ltd Spring steel with superior heat resistance

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Publication number Publication date
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