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JPS6041699B2 - Spring steel with excellent hardenability and fatigue resistance - Google Patents
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JPS6041699B2 - Spring steel with excellent hardenability and fatigue resistance - Google Patents

Spring steel with excellent hardenability and fatigue resistance

Info

Publication number
JPS6041699B2
JPS6041699B2 JP7463981A JP7463981A JPS6041699B2 JP S6041699 B2 JPS6041699 B2 JP S6041699B2 JP 7463981 A JP7463981 A JP 7463981A JP 7463981 A JP7463981 A JP 7463981A JP S6041699 B2 JPS6041699 B2 JP S6041699B2
Authority
JP
Japan
Prior art keywords
steel
resistance
spring steel
hardness
hardenability
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
Application number
JP7463981A
Other languages
Japanese (ja)
Other versions
JPS57188651A (en
Inventor
俊郎 山本
良平 小林
衛 栗本
敏夫 小曽根
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.)
Chuo Hatsujo KK
Aichi Steel Corp
Original Assignee
Chuo Hatsujo KK
Aichi 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 Chuo Hatsujo KK, Aichi Steel Corp filed Critical Chuo Hatsujo KK
Priority to JP7463981A priority Critical patent/JPS6041699B2/en
Priority to US06/289,852 priority patent/US4448617A/en
Priority to DE19813130914 priority patent/DE3130914A1/en
Publication of JPS57188651A publication Critical patent/JPS57188651A/en
Priority to US06/585,479 priority patent/US4574016A/en
Publication of JPS6041699B2 publication Critical patent/JPS6041699B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は焼入性、耐へたり性の優れたばね用鋼に関する
ものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a spring steel having excellent hardenability and resistance to settling.

近年、自動車軽量化の一環として懸架ばねの軽量化が強
く求められるようになつてきた。
In recent years, as part of efforts to reduce the weight of automobiles, there has been a strong demand for lighter suspension springs.

この要求に対して、ばねの設計応力を上昇させ、高応力
状態で使用することにより軽量化を図ることが効果的と
されている。しかし、現用のばね用鋼を高応力下で使用
すると、耐久性と、へたりが増加するという問題が生じ
、後者の「へたり」は、ばね高さの減少、しいては車高
の減少として現われ、バンパー高さが低下するため安全
上大きな問題となる。
In response to this demand, it is considered effective to increase the design stress of the spring and use it in a high stress state to reduce the weight. However, when current spring steel is used under high stress, problems arise in terms of durability and increased sagging. This results in a reduction in the height of the bumper, which poses a major safety problem.

そこで、近年高応力設計を可能とする耐へたり性の優れ
たばね用鋼が求められている。
Therefore, in recent years, there has been a demand for spring steel with excellent fatigue resistance that enables high-stress designs.

従来、耐へたり性の優れたばね用鋼としては、ばね鋼中
のSiが耐へたり性に有効な元素であるこ112L−、
、−ツ、゛−ムッ゛ CITDQ1、7を11+こl−
q書1の高いSUP7が多く用いられるようになつてき
た。
Conventionally, as a spring steel with excellent resistance to setting, Si in the spring steel is an effective element for resistance to setting.
,-tsu,゛-mu゛ CITDQ1, 7 to 11 + 1-
SUP7, which has a high q-book of 1, has come to be widely used.

しかるに、懸架ばねの軽量化に対する要求は厳しいもの
があり、SUP7よりもさらに耐へたり性の優れたばね
用鋼の開発が強く望まれていた。本願出願人はこのよう
な背景の下に、先に高Siばね用鋼に適量のV、Nbを
1種ないし2種添加することにより、SUP7よりもさ
らに耐へたり性が優れ、かつ、ばね用鋼として必要な耐
疲労性、靭性についてもSUP7と同等な性能を有する
ばね用鋼を開発して出願(特願昭55−10802賜)
した。しかし、比較的大型の自動車等に使用される大物
のコイルばね、トーシヨンバーおよび厚物の重ね板ばね
においては、熱処理時、芯部まで焼が入、り難いことに
より、芯部の組織はベイナイトあるいはフエライーパー
ライトとなり、マルテンサイト組織に比べて硬さが低く
、V、Nbによる耐へたり性向上効果が著しく損なわれ
る。
However, there are strict requirements for reducing the weight of suspension springs, and there has been a strong desire to develop a steel for springs that is even more resistant to fatigue than SUP7. Against this background, the applicant of the present application first added appropriate amounts of one or two types of V and Nb to high-Si spring steel, thereby creating a spring with even better fatigue resistance than SUP7. Developed and applied for a spring steel with performance equivalent to SUP7 in terms of fatigue resistance and toughness required for a spring steel (Patent Application No. 10802/1983)
did. However, in large coil springs, torsion bars, and thick stacked leaf springs used in relatively large automobiles, it is difficult to harden down to the core during heat treatment, so the structure of the core is bainite or The structure becomes ferrite pearlite, which has lower hardness than a martensitic structure, and the effect of improving the fatigue resistance due to V and Nb is significantly impaired.

本発明者等は、前記の大物または厚物のばねに)対して
も十分に耐へたり性を得るべき研究を重ねた結果、高S
iばね用鋼に適量のりあるいはV、Nbを添加するとと
もに、さらにBを添加し、かつNo、0080%以下と
することによつて大物のコイルばね、トーシヨンバーお
よび厚物の重ね板ばね5においても熱処理時、芯部まで
マルテンサイト組織が得られ、耐へたり性を損うことの
ない焼入性の優れたばね用鋼の開発に成功したものであ
る。
The present inventors have conducted research to obtain sufficient fatigue resistance even for the above-mentioned large or thick springs, and have found that
By adding an appropriate amount of glue, V, and Nb to the steel for springs, and further adding B, and making the amount less than 0.080%, it can be used even in large coil springs, torsion bars, and thick stacked leaf springs 5. During heat treatment, a martensitic structure is obtained up to the core, and we have successfully developed a spring steel with excellent hardenability that does not impair set resistance.

以下に本発明について詳述する。本発明は重量比にして
CO.5O−0.80%、Sil.5O〜2.50%、
MnO.5O〜1.50%と、VO.O5〜0.50%
あるいはVO.O5〜0.50%、NbO.O5〜0.
50%と、かつBO.OOO5〜0.01%を含有し、
さらにNO.OO8O%以下とし、残部実質的にFeよ
りなる焼入性、耐へたり性に優れ、かつ、耐疲労性、靭
性が良好なばね用鋼である。
The present invention will be explained in detail below. The present invention is CO. 5O-0.80%, Sil. 5O~2.50%,
MnO. 5O to 1.50% and VO. O5~0.50%
Or VO. O5~0.50%, NbO. O5~0.
50% and BO. Contains OOO5-0.01%,
Furthermore, NO. This is a spring steel with an OO of 80% or less and the remainder being substantially Fe, which has excellent hardenability and set resistance, as well as good fatigue resistance and toughness.

本発明鋼におけるV,NbおよびBの耐へたり性焼入性
向上機構を以下に説明する。
The mechanism for improving the setting resistance and hardenability of V, Nb and B in the steel of the present invention will be explained below.

V,Nbは鋼中において炭化物を形成し、このV炭化物
、Nb炭化物(以下、合金炭化物という)は、焼入れ時
に加熱に際してオーステナイト中に溶解し、焼入れによ
りマルテンサイト中に過飽和に固溶される。
V and Nb form carbides in steel, and these V carbides and Nb carbides (hereinafter referred to as alloy carbides) are dissolved in austenite during heating during quenching, and are supersaturated solid dissolved in martensite by quenching.

これを焼もどしすると、その過程で微細な合金炭化物が
再析出し、二次硬化を生じ、これが銅中において転位の
動きを阻止することにより耐へたり性を向上させる働き
をするものである。また、焼入れ時の加熱においてオー
ステナイト中に溶解されない合金炭化物は、オーステナ
イト結晶粒を微細化するとともにその粗大化を防止する
When this is tempered, fine alloy carbides re-precipitate during the process, causing secondary hardening, which functions to improve the resistance to settling by inhibiting the movement of dislocations in the copper. In addition, alloy carbides that are not dissolved in austenite during heating during quenching refine the austenite crystal grains and prevent them from becoming coarser.

このように微細化した結晶粒界は転位の移動−量を少な
くすることにより耐へたり性を向上させる。また、原子
状のBは焼入性に有効な働きをする。
The grain boundaries refined in this manner improve the resistance to settling by reducing the amount of movement of dislocations. In addition, atomic B has an effective effect on hardenability.

この原子状のBは鋼中において侵入型として結晶内に固
溶するもので、特に転位付近に侵入し.易い。このよう
にBが侵入した転位は移動が困難となることからへたり
減少に効果を有するものである。さらに、本発明鋼はN
b,■を含有することにより、通常のはね用銅の焼入れ
温度である900℃!から焼入れた場合においても、そ
の後の焼もどし過程で再析出し、2次硬化を生ずる。
This atomic B forms a solid solution in the crystals of steel as an interstitial type, and particularly penetrates near dislocations. easy. Since the dislocations into which B has invaded in this way become difficult to move, they are effective in reducing fatigue. Furthermore, the steel of the present invention has N
By containing b and ■, the quenching temperature of normal spring copper is 900℃! Even in the case of hardening, redeposition occurs during the subsequent tempering process, resulting in secondary hardening.

これは同一焼もどし硬さ範囲を狙う場合、従来鋼に比較
して焼もどし温度範囲をより広い範囲とすることが可能
であり、狙いの硬さが安定して得られることにクなる。
このことを、さらに明らかにするとともにBの作用につ
いて説明するため高Si鋼をベースとして、後述の0.
28%の■と0.0029%のBを含有させたA1鋼、
0.21%のVと0.09%のNb.l5O.OO2l
%のBを含有させたA2鋼、0.26%の■を含有させ
たB1鋼、さらに現用の高S1鋼であるC1鋼とを30
0〜600℃の間で焼もどしを行い、その硬さを測定し
た結果を第1図に示した。
This means that when aiming for the same tempering hardness range, it is possible to set the tempering temperature range to a wider range compared to conventional steel, and the target hardness can be stably obtained.
In order to further clarify this and explain the effect of B, we used high-Si steel as a base and 0.
A1 steel containing 28% ■ and 0.0029% B,
0.21% V and 0.09% Nb. l5O. OO2l
A2 steel containing 0.26% B, B1 steel containing 0.26% ■, and C1 steel, which is a currently used high S1 steel,
Tempering was performed at a temperature between 0 and 600°C, and the hardness was measured. The results are shown in Figure 1.

第1図から明らかなように、■,NbとBを含有させた
Al,A?判およびVを単独で含有させたB1鋼はとも
に、通常の900℃からの焼入れにおいても、二次硬化
の発生を示す硬さ増加のピークが550℃付近の焼もど
し温度)で認められる。これによりBの添加によりニ次
硬化の発生が阻害されないことは明らかであり、また現
用のばね用鋼の硬さ規定範囲(HRC45〜51)付近
の硬さを得るための焼もどし温度で、析出強化を十分利
用できることも明らかである。また、前記の鋼について
、焼入性温度850〜1100゜Cの範囲で順次高くし
、550′Cて焼もどしした時の硬さを第2図に示した
。これによりC1鋼を除いて、Al,M錆およびB1鋼
においては焼入れ温度が高くなるにしたがつて硬さが上
昇していることがわかる。これは上述したオーステナイ
ト相に溶解する合金炭化物が焼入れ温度の上昇にともな
い増加し、これによりニ次硬化が顕著に生じたことを物
語つている。さらに、前記の鋼について、850〜11
00℃の焼入温度で加熱し、酸化法により測定した、オ
ーステナイト結晶粒度を第3図に示した。
As is clear from Figure 1, ■, Al containing Nb and B, A? Even in the normal quenching from 900° C., a peak in hardness increase indicating the occurrence of secondary hardening is observed at a tempering temperature of around 550° C. for both B1 steel and B1 steel containing V alone. As a result, it is clear that the addition of B does not inhibit the occurrence of secondary hardening, and at the tempering temperature to obtain a hardness near the hardness regulation range (HRC 45 to 51) of current spring steels, precipitation occurs. It is also clear that reinforcement can be fully utilized. Further, the hardness of the above-mentioned steel is shown in FIG. 2 when the hardenability temperature is gradually increased in the range of 850 to 1100°C and tempered at 550'C. This shows that, with the exception of C1 steel, the hardness of Al, M rust, and B1 steels increases as the quenching temperature increases. This indicates that the amount of alloy carbides dissolved in the austenite phase increases as the quenching temperature rises, resulting in significant secondary hardening. Furthermore, for the above steel, 850 to 11
The austenite grain size measured by the oxidation method after heating at a quenching temperature of 00° C. is shown in FIG.

第3図から明らかなように、V,Nb(5Bを含有させ
たAl,A鋼は、Vを単独で含有させたB1鋼と同等の
オーステナイト結晶粒度を有しており、これよりB添加
により、合金炭化物による結晶粒の微細化オーステナイ
ト結晶粒の粗大化阻止作用が可等損なわれないことがわ
かる。また、前記の鋼のジョミニー曲線を第4図に示し
た。
As is clear from Figure 3, the Al, A steel containing V, Nb (5B) has the same austenite grain size as the B1 steel containing V alone, and from this it can be seen that the addition of B , it can be seen that the effect of the alloy carbides on refining the crystal grains and inhibiting the coarsening of the austenite crystal grains is not significantly impaired.Furthermore, the Jominy curve of the above-mentioned steel is shown in FIG.

第4図から明らかなようにBを含有させたAl,A潔は
、Bを含有しないB1鋼およびC1鋼に比較して、その
焼入性は飛躍的に向上していることがわかる。上述のよ
うに本発明鋼は高S1ばね用鋼に適量■,Nb(5Bを
併せて含有させることにより、合金炭化物による二次硬
化と結晶粒の微細化作用および原子状Bによる焼入性の
向上と転位の固定化の作用を利用して焼入性、耐へたり
性に優れたはね用鋼が得られたものである。
As is clear from FIG. 4, the hardenability of Al and A steel containing B is dramatically improved compared to B1 steel and C1 steel that do not contain B. As mentioned above, the steel of the present invention has a high S1 spring steel containing an appropriate amount of ■, Nb (5B), thereby improving secondary hardening and grain refinement by alloy carbides and hardenability by atomic B. A spring steel with excellent hardenability and set resistance was obtained by utilizing the effects of hardening and fixation of dislocations.

つぎに本発明鋼の成分限定理由について説明する。Next, the reasons for limiting the composition of the steel of the present invention will be explained.

C量を0.50〜0.80%としたのは0.50%以下
では焼入れ、焼もどしにより高応力ばね用鋼として十分
な強度が得られないためであり、0.80%を越えて含
有させると過共析鋼となり靭性の低下が著しくなるため
である。
The reason why the C content is set to 0.50 to 0.80% is because if it is less than 0.50%, sufficient strength cannot be obtained as a steel for high stress springs by quenching and tempering. This is because if it is contained, it becomes hypereutectoid steel, resulting in a significant decrease in toughness.

Sl量を1.50〜2.50%としたのは、1.50%
以下ではS】の有するフェライト中に固溶することによ
り素地の強度を上げ、耐へたり性を改善するという効果
が十分に得られないためであり、2.50%を越えて含
有させても耐へたり性向上の効果が飽和し、かつ、熱処
理により遊離炭素を生じる恐れがあるためである。
The reason for setting the Sl amount to 1.50 to 2.50% is 1.50%.
This is because the effect of increasing the strength of the base material and improving the resistance to settling by solid solution in the ferrite of S] cannot be sufficiently obtained, and even if it is contained in an amount exceeding 2.50%. This is because there is a possibility that the effect of improving the settling resistance is saturated and that free carbon is generated due to heat treatment.

Mn量を0.50〜1.50%としたのは、0.50%
以下ではばね用鋼としての強度が不足し、さらに焼入性
の点でも不十分であるためであり、1.50%を越えて
含有させると靭性を阻害するためである。
The Mn amount was set to 0.50 to 1.50% by 0.50%.
This is because if the content is less than 1.5%, the strength as a spring steel is insufficient, and the hardenability is also insufficient, and if the content exceeds 1.50%, the toughness will be impaired.

■,Nbはいずれも本発明鋼においては耐へたり性を改
善する元素である。このような働きを奏する■,Nbの
含有量をそれぞれ0.05〜0.50%としたのは、0
.05%以下ては上記の効果が十分に得られないためで
あり、0.50%を越えて含有させてもその効果が飽和
し、かつ、オーステナイト中に溶解されない合金炭化物
が増加し、大きな塊となることにより非金属介在物的な
作用により鋼の疲労強度を低下させる恐れがあるためで
ある。
(2) and Nb are both elements that improve the sag resistance in the steel of the present invention. The content of ■ and Nb, which play this role, was set at 0.05% to 0.50%, respectively.
.. This is because if the content is less than 0.50%, the above effect cannot be obtained sufficiently, and if the content exceeds 0.50%, the effect will be saturated, and the amount of alloy carbides that will not be dissolved in the austenite will increase, resulting in large lumps. This is because the fatigue strength of the steel may be reduced due to the action of nonmetallic inclusions.

これらの■,Nbは2種を複合添加することにより、V
,Nbを単独で添加した場合に比べ、より低い温度でオ
ーステナイト中への溶解を開始させ、また焼もどし過程
において微細な合金炭化物の析出は、二次硬化をより促
進させることにより耐へたり性をさらに向上させるもの
である。
By adding these two types in combination, V and Nb can be
, Nb starts to dissolve into austenite at a lower temperature than when it is added alone, and the precipitation of fine alloy carbides during the tempering process promotes secondary hardening, which improves the resistance to setting. This further improves the

B量を0.0005〜0.01%としたのは、0.00
05%以下では焼入性向上効果および耐へたり性減少効
果が十分に得られないためであり、0.01%を越えて
含有させるとボロン化合物が析出し、熱間脆性が現われ
るためである。N量を0.0080%以下としたのは、
BがNと結合し、原子状のBが減少することにより、B
の効果が損なわれるのを防止するためてある。
The amount of B was set to 0.0005 to 0.01% because 0.00
This is because if the content is less than 0.05%, the effect of improving hardenability and reducing the fatigue resistance cannot be sufficiently obtained, and if the content exceeds 0.01%, boron compounds will precipitate and hot embrittlement will appear. . The reason why the N amount was set to 0.0080% or less was because
By combining B with N and reducing atomic B, B
This is to prevent the effects from being impaired.

つきに本発明鋼の特徴を、比較鋼、従来鋼と比べ実施例
でもつて明らかにする。
At the same time, the characteristics of the steel of the present invention will be clarified by comparing it with comparative steels and conventional steels through examples.

第1表はこれらの供試鋼の化学成分を示すものてある。Table 1 shows the chemical composition of these test steels.

第1表においてAl,A潔は本発明鋼で、Bl,B2は
高S]銅に■,Nbを添加した比較鋼で、C1は従来鋼
てSUP7てある。なお、Al,A2鋼、Bl,B2鋼
およびC1鋼に含有される0.11〜0.13%のCr
量は原材料より混入したものでいずれも不純物量である
In Table 1, Al and A are the steels of the present invention, Bl and B2 are comparative steels made of high S] copper with ■ and Nb added, and C1 is the conventional steel SUP7. In addition, 0.11 to 0.13% Cr contained in Al, A2 steel, Bl, B2 steel and C1 steel
All amounts are amounts of impurities mixed in from raw materials.

第2表は鋳造後、圧延比50以上で熱間圧延を施した第
1表の供試鋼を、焼もどし硬さがI(RC48程度にな
るよう熱処理を行い、この時の引張り強さ、0.2%耐
力、伸び、絞り、衝撃値、ねじり強さを示したものであ
る。
Table 2 shows the test steels in Table 1 that were hot-rolled at a rolling ratio of 50 or more after casting, and were heat-treated to have a tempering hardness of about I (RC48). 0.2% proof stress, elongation, reduction of area, impact value, and torsional strength are shown.

引張強さ、0.2%耐力、伸び、絞りについては、JI
S4号試験片を用いて測定したものであり、衝撃値はJ
IS3号試験片を用いて測定し、ねじり強さは平行部9
TWL丸の試験片を用いて測定したものである。
For tensile strength, 0.2% proof stress, elongation, and area of area, please refer to JI
It was measured using a No. S4 test piece, and the impact value was J
Measured using an IS3 test piece, and the torsional strength was 9 in the parallel part.
This was measured using a test piece with a TWL circle.

第2表により明らかなようにBを添加した本発明鋼であ
るAl,A′$uは、■,Nbを添加した比較鋼である
Bl,B2鋼と同等な機械的性質を示し、従来鋼である
C1鋼に比べて0.2%耐力が優れているものである。
As is clear from Table 2, B-added steels of the present invention, Al and A'$u, exhibit mechanical properties equivalent to Bl and B2 steels, which are comparison steels with ■ and Nb added, and the conventional steels It has a 0.2% yield strength superior to that of C1 steel.

つぎに前記供試鋼を素材として、第3表に示す諸元を有
する平行部径307S!lφのトーシヨン・バーを製作
し、最終硬さがHRC45〜55となるように焼入れ、
焼もどし処理を行つた後、ショットピーニング処理を施
し、へたり試験片とした。へたり試験に先立って、試験
片平行部の表面に剪断応力γ=110k9f/WrlL
が現われるようなトルクを両端に付加し、セツチングを
施した。セツチングの後剪断応力τ=100k9f/i
となるトルクを加え、そのまま961寺間放置し、その
後、ねじれ角度の減少量からYR=ΔQ−d/21に従
つて残留剪断歪量を求めた。上記試験片の硬さに対する
へたり量を第5図に示した。
Next, using the above-mentioned test steel as a material, the diameter of the parallel part is 307S with the specifications shown in Table 3! A torsion bar of lφ was manufactured and quenched to a final hardness of HRC45 to 55.
After the tempering treatment, shot peening treatment was performed to obtain a set test piece. Prior to the settling test, a shear stress γ = 110k9f/WrlL was applied to the surface of the parallel part of the specimen.
Torque was added to both ends to create a setting. Shear stress after setting τ=100k9f/i
A torque of 961 was applied, and the sample was left as it was, and then the amount of residual shear strain was determined from the amount of decrease in twist angle according to YR=ΔQ−d/21. FIG. 5 shows the amount of set in relation to the hardness of the test piece.

第5図から明らかなようにBを含有する本発明鋼Al,
A2から作製した平行部径30Twtφの試験片のへた
り量は、従来鋼であるC1鋼よりも非常に優れており、
また比較鋼であるB1鋼と比較しても良い値を示してい
る。これはBを含有させたことにより、30Tf$tφ
のトーシヨン・バーにおいても焼入れ処理により芯部ま
で完全にマルテンサイトの硬化組織を得ることができ耐
へたり性がノ損なわれなかつたことと、Bが侵入型とし
て結晶内、転位付近に侵入し、転位の移動が困難となる
ことによりへたり減少に効果があつたものと考えられる
。さらに、本発明鋼であるAl,A2鋼、比較鋼で・あ
るBl,B@から作製した上記トーシヨン・バーに対し
て、剪断応力60±50kgf/Tf7ltで繰り返し
負荷を与え疲労試験を行つた結果、いずれのトーシヨン
・バーも20万回繰り返し負荷を与えても折損しなくB
添加による疲れ寿命に対する影響のなlいことが確認さ
れた。
As is clear from FIG. 5, the present invention steel Al containing B,
The amount of settling of a test piece with a parallel part diameter of 30Twtφ made from A2 is much better than that of C1 steel, which is a conventional steel.
It also shows good values when compared with B1 steel, which is a comparative steel. This is due to the inclusion of B, resulting in 30Tf$tφ
In the torsion bar, a hardened martensite structure was obtained completely down to the core through quenching, and the fatigue resistance was not impaired. This is thought to be effective in reducing fatigue by making it difficult for dislocations to move. Furthermore, the results of a fatigue test were conducted by repeatedly applying a shear stress of 60±50 kgf/Tf7lt to the above-mentioned torsion bars made from Al and A2 steels, which are the steels of the present invention, and Bl and B@, which are comparative steels. , all torsion bars do not break even after being repeatedly loaded 200,000 times.B
It was confirmed that the addition had no effect on fatigue life.

上述の如く本発明鋼は従来の高S1ばね用鋼に適量の■
あるいは■,Nbを添加させるとともにBを含有し、さ
らにNを0.0080%以下とすることにより、従来の
高S1はね用鋼の焼入性、耐へたり性を大巾に改善する
ことに成功したもので、かつ、ばね用鋼として必要な耐
疲労性、靭性についても従来鋼と比べそん色のないもの
で、特に乗用車懸架ばね用鋼として極めて高い実用性を
有するものである。
As mentioned above, the steel of the present invention has an appropriate amount of ■
Or ■, by adding Nb and containing B, and further reducing N to 0.0080% or less, the hardenability and settling resistance of conventional high S1 splash steel can be greatly improved. Furthermore, it has the same fatigue resistance and toughness as conventional steels, which are necessary for spring steel, and has extremely high practicality, especially as a steel for passenger car suspension springs.

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

第1図は本発明鋼、比較鋼、および従来鋼について焼入
れ後、300〜600℃の間で焼もどしを行い、その硬
さを示した線図、第2図は第4図の鋼を850〜120
0℃の温度から油中に焼入れし、その後550′Cで焼
もどしをした時の硬さを示した線図、第3図は第1図の
鋼を850〜1100′Cの焼入れ温度で加熱した場合
のオーステナイト結晶粒度を示した線図、第4図は第1
図の鋼について焼入性を示した線図、第5図は本発明鋼
、比較鋼および従来鋼について焼入れ、焼もどし処理後
、11RC45〜55の硬さの試験片のへたり量を示し
た線図である。
Figure 1 is a diagram showing the hardness of the steel of the present invention, comparative steel, and conventional steel after being quenched and then tempered between 300 and 600°C. ~120
A diagram showing the hardness when quenched in oil from a temperature of 0℃ and then tempered at 550'C. Figure 3 shows the hardness of the steel shown in Figure 1 heated at a quenching temperature of 850 to 1100'C. Figure 4 is a diagram showing the austenite grain size when
Figure 5 is a diagram showing the hardenability of the steel shown in the figure. Figure 5 shows the amount of set in test pieces with a hardness of 11RC45 to 55 after quenching and tempering for the inventive steel, comparative steel, and conventional steel. It is a line diagram.

Claims (1)

【特許請求の範囲】[Claims] 1 重量比にしてC0.50〜0.80%、Si1.5
0〜2.50%、Mn0.50〜1.50%と、V0.
05〜0.50%あるいはV0.05〜0.50%、N
b0.05〜0.50%と、かつB0.0005〜0.
01%を含有し、さらにN0.0080%以下とし、残
り実質的にFeよりなることを特徴とする焼入性、耐へ
たり性の優れたばね鋼。
1 Weight ratio: C0.50-0.80%, Si1.5
0 to 2.50%, Mn 0.50 to 1.50%, and V0.
05-0.50% or V0.05-0.50%, N
b0.05-0.50%, and B0.0005-0.
A spring steel having excellent hardenability and fatigue resistance, characterized in that it contains N0.001%, N0.0080% or less, and the remainder substantially consists of Fe.
JP7463981A 1980-08-05 1981-05-16 Spring steel with excellent hardenability and fatigue resistance Expired JPS6041699B2 (en)

Priority Applications (4)

Application Number Priority Date Filing Date Title
JP7463981A JPS6041699B2 (en) 1981-05-16 1981-05-16 Spring steel with excellent hardenability and fatigue resistance
US06/289,852 US4448617A (en) 1980-08-05 1981-08-04 Steel for a vehicle suspension spring having good sag-resistance
DE19813130914 DE3130914A1 (en) 1980-08-05 1981-08-05 STEEL FOR VEHICLE SUSPENSION SPRINGS WITH HIGH RESISTANCE TO INCREASING BENDING OR BENDING. Sagging
US06/585,479 US4574016A (en) 1980-08-05 1984-03-02 Method of treating steel for a vehicle suspension spring having a good sag-resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP7463981A JPS6041699B2 (en) 1981-05-16 1981-05-16 Spring steel with excellent hardenability and fatigue resistance

Publications (2)

Publication Number Publication Date
JPS57188651A JPS57188651A (en) 1982-11-19
JPS6041699B2 true JPS6041699B2 (en) 1985-09-18

Family

ID=13552976

Family Applications (1)

Application Number Title Priority Date Filing Date
JP7463981A Expired JPS6041699B2 (en) 1980-08-05 1981-05-16 Spring steel with excellent hardenability and fatigue resistance

Country Status (1)

Country Link
JP (1) JPS6041699B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5996246A (en) * 1982-11-22 1984-06-02 High Frequency Heattreat Co Ltd Steel wire for cold formed spring of extra high strength its production and cold formed spring of extra high strength obtained from said steel wire
JPS59170241A (en) * 1983-03-18 1984-09-26 Daido Steel Co Ltd Steel for high-strength and high-toughness spring
JP2860789B2 (en) * 1987-04-30 1999-02-24 愛知製鋼 株式会社 Spring steel with excellent hardenability and durability
CN111321346B (en) * 2020-03-05 2021-12-24 马鞍山钢铁股份有限公司 Ultrahigh-strength spring steel with excellent hydrogen-induced delayed fracture resistance and production method thereof

Also Published As

Publication number Publication date
JPS57188651A (en) 1982-11-19

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