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JPS6237108B2 - - Google Patents
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JPS6237108B2 - - Google Patents

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Publication number
JPS6237108B2
JPS6237108B2 JP56126281A JP12628181A JPS6237108B2 JP S6237108 B2 JPS6237108 B2 JP S6237108B2 JP 56126281 A JP56126281 A JP 56126281A JP 12628181 A JP12628181 A JP 12628181A JP S6237108 B2 JPS6237108 B2 JP S6237108B2
Authority
JP
Japan
Prior art keywords
steel
steels
resistance
fatigue
spring
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
JP56126281A
Other languages
Japanese (ja)
Other versions
JPS5827959A (en
Inventor
Toshiro Yamamoto
Ryohei Kobayashi
Mamoru Kurimoto
Toshio Kosone
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 JP12628181A priority Critical patent/JPS5827959A/en
Publication of JPS5827959A publication Critical patent/JPS5827959A/en
Publication of JPS6237108B2 publication Critical patent/JPS6237108B2/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]

本発明は耐へたり性の優れたばね用鋼に関する
ものである。 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。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反応下で使用する
と、耐久性が低下し、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れ、バンパー高
さが低下するた安全上大きな問題となる。 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。 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
とが知られるにつれて、CUP6よりもさらにSi
量の高いSUP7が多く用いられるようになつてき
た。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、Moを1種ないし2種
以上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55−108020
号)した。 本発明はこのような背景の下に、本発明者等が
研究を重ねた結果、高Siばね用鋼に適量のVある
いはVとNbを添加するとともに結晶粒度を微細
化するA1を添加させことにより耐へたり性をさ
らに向上させることに成功したものである。 また、本発明は必要に応じてBを添加して焼入
性を向上させ、かつ、Niを添加して焼入性に加
えて靭性を向上させるものであり、本発明は耐へ
たり性のみならず焼入性、靭性についても優れた
もので、かつ、ばね用鋼として必要な耐疲労性に
ついてもSUP7と同等の性能を有するものであ
る。 以下に本発明について詳述する。 第1発明鋼は、重量比にしてC0.50〜0.80%、
Si1.50〜2.50%、Mn0.70〜1.50%と、V0.20〜0.50
%あるいはV0.20〜0.50%、Nb0.05〜0.15%を含
有し、さらにAl0.03〜0.10%を含有したもので、
第2発明は第1発明にさらにB0.0005〜0.0020
%、Ni0.20〜0.50%を含有させ第1発明鋼の焼入
性、靭性を向上させたものである。本発明鋼にお
けるV、Nbの耐へたり性向上機構を以下に説明
する。 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、焼入れ時の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。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、これが鋼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くをするも
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。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。 さらに、本発明鋼はNb、Vを含有することに
より、通常のばね用鋼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。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
なる。 また、Alは結晶粒微細化元素で、鋼中におい
て多くの場合窒化物を形成し、焼入れ時の加熱に
おいてこの窒化物がオーステナイト結晶粒の粗大
化を防止し得る。そして、このような微細な結晶
粒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。 さらに、焼入性を向上させるB、Niのうち、
特にBは耐へたり性にも有効な元素である。 すなわち、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が侵入した転位は転動が
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、比較的大型の自動車等に使用される太
物のコイルばね、トーシヨンバーおよび厚物の重
ね板ばねにおいても、B、Niの焼入性向上元素
を添加させることにより熱処理時、芯部までマル
テンサイト組織が得られ、耐へたり性を損なうこ
とがないものである。 以下に本発明鋼の成分限定理由について説明す
る。 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。 Si量を1.50〜2.50%としたのは、1.50%以下で
はSiの有するフエ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。 Mn量を0.70〜1.50%としたのは、0.70%以下で
は焼入性が不足して十分な強度が得られないため
でであり、1.50%を越えて含有させると靭性を阻
害するためである。 V、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V、Nbの含有量につ
いて、V0.20〜0.50%、Nb0.05〜0.15%としたの
は、Vが0.20%未満、Nbについては0.05%未満で
は上記の効果が十分に得られないためであり、か
つWが0.50%を越えて、Nbが0.15%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量が増加し、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。 これらのV、Nbはそれぞれを単独で添加する
ほかに、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。 Alは鋼中において微細な窒化物を形成し、こ
れがオーステナイト結晶粒界の移動を妨げること
により、結晶粒度の微細化を達成するものであ
る。Alを0.03〜0.10%としたのは、下限以下では
十分な結晶粒微細化を達成するだけの窒化物が得
られないためであり、0.10%を越えて添加しても
結晶粒微細化作用が飽和するとともに、窒化物が
粗大化し、耐久性の点から好ましくないためであ
る。 Bは焼入性を向上させる元素である。 B量を0.0005〜0.0020%としたのは、0.0005%
以下では焼入性向上効果および耐へたり性向上効
果が十分に得られないためであり、0.0020%を越
えて含有させるとボロン化合物が析出し、熱間脆
性が現れるためである。 Niは本発明鋼においては焼入性および靭性を
改善する元素である。 Niを0.20〜0.50%としたのは、通常電気炉を溶
製した鋼中には不純物としてNiが0.110%程度含
有されており、かつ、本発明において0.20%以下
では焼入性および靭性改善効果が不十分であり、
0.50%を越えて含有させても効果が飽和し、かつ
残留オーステナイトを形成する恐れがあるためで
ある。 つぎに本発明鋼の特徴を従来鋼と比べ実施例で
もつて明らかにする。 第1表は、これらの供試鋼の化学成分を示すも
のである。
The present invention relates to a spring steel with excellent resistance to fatigue. In recent years, as part of efforts to reduce the weight of automobiles, there has been a strong demand for lighter suspension springs. 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 reaction conditions, problems arise such as decreased durability and increased sag. This appears as a decrease in the bumper height, which poses a major safety problem. Therefore, in recent years, there has been a demand for spring steel with excellent fatigue resistance that enables high-stress designs. Traditionally, spring steels with excellent resistance to fatigue include:
As it is known that Si in spring steel is an effective element for fatigue resistance, Si is used even more than CUP6.
SUP7, which has a high volume, is becoming more and more used. 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 first developed a high-Si
By adding appropriate amounts of one or more of V, Nb, and Mo to spring steel, it has even better fatigue resistance than SUP7, and also has the same fatigue resistance and toughness as SUP7, which is necessary for spring steel. Developed and applied for spring steel with equivalent performance (patent application 1982-108020)
No.). Against this background, the present invention was developed as a result of repeated research by the inventors and others, and was developed by adding an appropriate amount of V or V and Nb to high-Si spring steel, as well as adding A1 to refine the grain size. As a result, we succeeded in further improving the resistance to sagging. In addition, the present invention improves hardenability by adding B as needed, and improves toughness in addition to hardenability by adding Ni. It also has excellent hardenability and toughness, and has the same performance as SUP7 in terms of fatigue resistance, which is necessary for spring steel. The present invention will be explained in detail below. The first invention steel has C0.50 to 0.80% by weight,
Si1.50~2.50%, Mn0.70~1.50%, V0.20~0.50
% or V0.20-0.50%, Nb0.05-0.15%, and Al0.03-0.10%,
The second invention is B0.0005 to 0.0020 in addition to the first invention.
% and 0.20 to 0.50% of Ni to improve the hardenability and toughness of the first invention steel. The mechanism for improving the settling resistance of V and Nb in the steel of the present invention will be explained below. 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 become a supersaturated solid solution in martensite by quenching. . When this is tempered, fine alloy carbides re-precipitate during the process, causing secondary hardening, which works to improve the resistance to settling by inhibiting the movement of dislocations in the steel. 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. The grain boundaries refined in this manner improve the settling resistance by reducing the amount of movement of dislocations. Furthermore, by containing Nb and V, the steel of the present invention can be heated to a temperature of 900℃, which is the quenching temperature of ordinary spring steel.
Even in the case of hardening, redeposition occurs during the subsequent tempering process, resulting in secondary hardening. 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 targeted hardness can be stably obtained. Furthermore, Al is a grain refining element and often forms nitrides in steel, and these nitrides can prevent austenite grains from becoming coarse during heating during quenching. Such fine crystal grains improve the resistance to settling by reducing the amount of movement of dislocations. Furthermore, among B and Ni, which improve hardenability,
In particular, B is an element that is effective for resistance to settling. That is, atomic B forms a solid solution in the crystals of steel as an interstitial type, and is particularly likely to enter near dislocations. Since the dislocations into which B has invaded in this way make it difficult to roll, they are effective in reducing fatigue. Furthermore, even in thick coil springs, torsion bars, and thick stacked leaf springs used in relatively large automobiles, by adding hardenability-improving elements such as B and Ni, martin is added to the core during heat treatment. A site structure can be obtained without impairing the resistance to settling. The reasons for limiting the composition of the steel of the present invention will be explained below. The reason why the C content is set at 0.50 to 0.80% is that if it is less than 0.50%, sufficient strength cannot be obtained as a steel for high stress springs through quenching and tempering. This is because the decrease in toughness becomes significant. The reason why the amount of Si is set at 1.50 to 2.50% is because if it is less than 1.50%, the effect of increasing the strength of the base material and improving the resistance to settling cannot be obtained sufficiently by solid solution of Si in the ferrite. This is because even if the content exceeds 2.50%, the effect of improving the resistance to settling is saturated, and there is a risk that free carbon may be generated by heat treatment. The reason for setting the Mn content to 0.70 to 1.50% is because if it is less than 0.70%, hardenability is insufficient and sufficient strength cannot be obtained, and if it is contained in excess of 1.50%, toughness will be inhibited. . Both V and Nb are elements that improve the sag resistance in the steel of the present invention. Regarding the content of V and Nb, which have these functions, we set the content to 0.20 to 0.50% for V and 0.05 to 0.15% for Nb because the above effects are sufficient when V is less than 0.20% and Nb is less than 0.05%. However, even if W exceeds 0.50% and Nb exceeds 0.15%, the effect is saturated, and the amount of alloy carbides that are not dissolved in austenite increases, resulting in large lumps. This is because the fatigue strength of the steel may be reduced due to the action of nonmetallic inclusions. These V and Nb can be added individually or by adding the two in combination.
Compared to when Nb is added alone, dissolution into austenite starts at a lower temperature, and the precipitation of fine alloy carbides during the tempering process is
By further promoting secondary curing, the sagging resistance is further improved. Al forms fine nitrides in steel, which prevent the movement of austenite grain boundaries, thereby achieving refinement of grain size. The reason why Al is set at 0.03 to 0.10% is because if it is below the lower limit, it is not possible to obtain enough nitride to achieve sufficient grain refinement, and even if it is added above 0.10%, the grain refinement effect will not be obtained. This is because as it becomes saturated, the nitride becomes coarser, which is unfavorable from the viewpoint of durability. B is an element that improves hardenability. The amount of B is 0.0005% to 0.0020%, which means 0.0005%.
This is because the effect of improving hardenability and the effect of improving setting resistance cannot be sufficiently obtained if the content is below 0.0020%, and if the content exceeds 0.0020%, boron compounds will precipitate and hot embrittlement will appear. Ni is an element that improves hardenability and toughness in the steel of the present invention. The reason why Ni is set at 0.20 to 0.50% is because steel made in an electric furnace normally contains about 0.110% Ni as an impurity, and in the present invention, if it is less than 0.20%, it has an effect on improving hardenability and toughness. is insufficient,
This is because even if the content exceeds 0.50%, the effect will be saturated and there is a risk of forming retained austenite. Next, the characteristics of the steel of the present invention will be clarified through examples in comparison with conventional steel. Table 1 shows the chemical composition of these test steels.

【表】 第1表においてA1、A3、A6鋼は本発明鋼で、
A1、A3鋼は第1発明鋼、A6鋼は第2発明鋼で、
B1鋼は従来鋼でSUP7である。 鋳造後、圧延比50以上で熱間圧延を施した第1
表の供試鋼のうちA1、A3鋼、B1鋼を素材として
第2表に示す諸元を有するコイルばねを成形し、
最終硬さがHRC45〜55となるように焼入・焼も
どし処理を行つた後、素線の剪断応力τ=115
Kg/mm2となるようにセツチングを加えてへたり試
験片を作製した。そしてこの試験片を20℃の一定
温度で、素線の剪断応力τ=105Kg/mm2となる荷
重を加え、96時間経過(以下、これを長期荷重と
いう)した後のコイルばねのへたり量を測定し
た。
[Table] In Table 1, A1, A3, and A6 steels are the steels of the present invention.
A1 and A3 steels are the first invention steels, A6 steels are the second invention steels,
B1 steel is a conventional steel with SUP7. After casting, the first part was hot rolled at a rolling ratio of 50 or more.
Among the test steels in the table, A1, A3 steel, and B1 steel are used as raw materials to form a coil spring having the specifications shown in Table 2.
After quenching and tempering so that the final hardness is HRC45-55, the shear stress of the wire is τ = 115
A setting test piece was prepared by setting the weight to Kg/mm 2 . Then, a load was applied to this test piece at a constant temperature of 20°C so that the shear stress of the wire was τ = 105Kg/ mm2 , and the amount of fatigue of the coil spring after 96 hours (hereinafter referred to as long-term load) was measured.

【表】 そして、上記試験片の硬さに対するへたり量を
第1〜2図に示した。第1〜2図より明らかなよ
うに本発明鋼であるV、Nbを添加するとともに
A1、を添加したA1、A3鋼は、いずれも従来鋼で
あるB1鋼に比べ優れた耐へたり性を有している
ことが認められる。そして、本発明鋼の中でも
V、Nbを複合添加した鋼は、Vを単独添加した
鋼よりさらにすぐれた耐へたり性を有しているこ
とが分る。 なお、へたり量は前記長期荷重を加える前にコ
イルばねを一定の高さまで圧縮するに要した荷重
P1と、前記長期荷重を加えた後に同一の高さまで
圧縮するに要した荷重P2を測定し、その差△P
(=P1−P2)より次式を用いて算出したもので、剪
断ひずみの単位を有し、残留剪断ひずみと称する
値をもつて評価した。 γR=1/G・K8D/πd△P G:横弾性率(Kgf/mm2) D:コイル中心径(mm) d:素線径(mm) K:ワールの修正係数(コイルばねの形状により
定める定数) また、本発明鋼のA1、A3鋼、B1鋼について前
記と同じ諸元を有するコイルばね素線に、剪断応
力が10〜110Kgf/mm2と変動する負荷を繰返し与
え疲労試験を行つた結果、いずれのコイルばねも
20万回繰り返しても折損しなかつた。 つぎに、A6鋼、B1鋼を素材として、第3表に
示す諸元を有する平行部径30mmφ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、シヨツト
ピーニング処理を施し、へたり試験片とした。へ
たり試験に先立つて、試験片平行部の表面に剪断
応力τ=110Kgf/mm2が現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=100Kgf/mm2となるトルクを加
え、そのまま96時間放置し、その後、ねじり角度
の減少量からYR=△θ・d/2に従つて残留
剪断歪量を求めた。
[Table] Figures 1 and 2 show the amount of set in relation to the hardness of the test piece. As is clear from Figures 1 and 2, when adding V and Nb, which is the steel of the present invention,
It is recognized that both A1 and A3 steels to which A1 has been added have superior fatigue resistance compared to B1 steel, which is a conventional steel. It can be seen that among the steels of the present invention, the steel to which V and Nb are added in combination has better resistance to settling than the steel to which V is added alone. The amount of setback is the load required to compress the coil spring to a certain height before applying the long-term load.
Measure P 1 and the load P 2 required to compress to the same height after applying the long-term load, and calculate the difference △P
(=P 1 −P 2 ) using the following formula, and has a unit of shear strain, and was evaluated using a value called residual shear strain. γR=1/G・K8D/πd 3 △PG G: Transverse elastic modulus (Kgf/mm 2 ) D: Coil center diameter (mm) d: Wire diameter (mm) K: Whirl correction coefficient (shape of coil spring In addition, a fatigue test was conducted by repeatedly applying a load with a shear stress varying from 10 to 110 Kgf/mm 2 to coil spring wires having the same specifications as above for A1, A3 steel, and B1 steel of the present invention steel. As a result, both coil springs
It did not break even after being repeated 200,000 times. Next, using A6 steel and B1 steel as materials, a torsion with a parallel part diameter of 30 mmφ and having the specifications shown in Table 3 was prepared.
A bar was manufactured, quenched and tempered to a final hardness of HRC45 to 55, and shot peened to obtain a set test piece. Prior to the settling test, a torque was applied to both ends of the parallel portion of the test piece so that a shear stress τ = 110 Kgf/mm 2 appeared on the surface of the parallel portion, and setting was performed. After setting, a torque was applied to make the shear stress τ = 100Kgf/mm 2 , and it was left as it was for 96 hours, and then the amount of residual shear strain was determined from the amount of decrease in the twist angle according to YR = △θ・d/2. .

【表】 上記試験片の硬さに対するへたり量を第3図に
示した。第3図から明らかなようにBを含有する
本発明鋼A6から作製した平行部径30mmφの試験
片のへたり量は、従来鋼であるB1鋼よりも非常
に優れている。これは、Bを含有させたことによ
り、30mmφ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。 また、供試鋼のうち、A6鋼およびB1鋼のジヨ
ミニー曲線を第4図に示した。第4図から明らか
なようにBを含有させたA6鋼は、それを含有し
ないB1鋼と比較して、その焼入性は飛躍的に向
上していることがわかる。 さらに、供試鋼のうちA1、A3鋼およびB1鋼に
ついて、85〜1100℃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5
図に示した。第5図から明らかなように、V、
NbおよびA1を含有させたA1、A3鋼は、それら
を含有しないB1鋼に比べて優れたオーステナイ
ト結晶粒度を有している。 さらに、本発明鋼であるA6鋼、従来鋼、B1鋼
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/mm2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いことが確認さ
れた。 上述の如く本発明鋼は従来の高Siばね用鋼に適
量のV、Nbを単独あるいは複合して添加させる
ととも、Alを含有し、さらに必要に応じてB、
Niの2種を含有し、従来の高Siばね用鋼の耐へた
り性、焼入性を大幅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。
[Table] Figure 3 shows the amount of set in relation to the hardness of the above test piece. As is clear from FIG. 3, the amount of sag of the test piece with a diameter of 30 mm in the parallel portion made from the steel A6 of the present invention containing B is much better than that of the conventional steel B1. This is because by including B, even in a 30 mmφ torsion bar, a hardened martensite structure can be obtained completely up to the core through quenching, and the resistance to set- ting is not impaired. It is thought that this is effective in reducing fatigue by entering into the crystal and near dislocations as an interstitial type, making it difficult for dislocations to move. Furthermore, among the test steels, the Giyominy curves of A6 steel and B1 steel are shown in Fig. 4. As is clear from FIG. 4, the hardenability of A6 steel containing B is dramatically improved compared to B1 steel that does not contain B. Furthermore, among the test steels, A1, A3 steel, and B1 steel were heated at a quenching temperature of 85 to 1100℃, and the austenite grain size was measured by an oxidation method.
Shown in the figure. As is clear from Fig. 5, V,
The A1 and A3 steels containing Nb and A1 have superior austenite grain size compared to the B1 steel that does not contain them. Furthermore, the above torsion bars made from A6 steel, conventional steel, and B1 steel, which are the steels of the present invention, were subjected to a fatigue test by repeatedly applying a shear stress of 60±50 Kgf/ mm2 . Bar too
No breakage occurred even after repeated loading 200,000 times, confirming that the addition of B had no effect on fatigue life. As mentioned above, the steel of the present invention is made by adding appropriate amounts of V and Nb singly or in combination to conventional high-Si spring steels, and also contains Al, and further contains B, if necessary.
It contains two types of Ni, and has succeeded in significantly improving the fatigue resistance and hardenability of conventional high-Si spring steels, and also has the fatigue resistance and toughness required for spring steels. It is also comparable to conventional steel,
In particular, it has extremely high practicality as a steel for suspension springs for passenger cars.

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

第1〜3図は本発明鋼、従来鋼について焼入
れ、焼もどし処理後、HRC45〜55の硬さの試験
片のへたり量を示した線図、第4図はA6、B1鋼
について焼入性を示した線図、第5図はA1〜
A3、B1鋼について850〜1100℃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
図である。
Figures 1 to 3 are graphs showing the amount of settling of test specimens with hardness of HRC45 to 55 after quenching and tempering for the present invention steel and conventional steel, and Figure 4 is for A6 and B1 steels after quenching. Diagram showing gender, Figure 5 is A1~
It is a diagram showing the austenite grain size when A3 and B1 steels are heated at a quenching temperature of 850 to 1100°C.

Claims (1)

【特許請求の範囲】 1 重量比にしてC0.50〜0.80%、Si1.50〜2.50
%、Mn0.70〜1.50%と、V0.20〜0.50%あるいは
V0.20〜0.50%、Nb0.05〜0.15%を含有し、さら
にAl0.03〜0.10%を含有させ、残り実質的にFeよ
りなることを特徴とする耐へたり性の優れたばね
用鋼。 2 重量比にしてC0.50〜0.80%、Si1.50〜2.50
%、Mn0.70〜1.50%と、V0.20〜0.50%を含有
し、さらにAl0.03〜0.10%と、B0.0005〜0.0020
%、Ni0.20〜0.50%を含有させ、残り実質的にFe
よりなることを特徴とする耐へたり性の優れたば
ね用鋼。
[Claims] 1. C0.50-0.80%, Si1.50-2.50 in terms of weight ratio
%, Mn0.70~1.50% and V0.20~0.50% or
A spring steel with excellent fatigue resistance characterized by containing 0.20 to 0.50% of V, 0.05 to 0.15% of Nb, and further containing 0.03 to 0.10% of Al, with the remainder substantially consisting of Fe. 2 C0.50~0.80%, Si1.50~2.50 by weight
%, Mn0.70~1.50%, V0.20~0.50%, and Al0.03~0.10%, B0.0005~0.0020
%, Ni 0.20-0.50%, and the rest is substantially Fe.
Spring steel with excellent fatigue resistance.
JP12628181A 1981-08-11 1981-08-11 Spring steel with superior yielding resistance Granted JPS5827959A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP12628181A JPS5827959A (en) 1981-08-11 1981-08-11 Spring steel with superior yielding resistance

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP12628181A JPS5827959A (en) 1981-08-11 1981-08-11 Spring steel with superior yielding resistance

Publications (2)

Publication Number Publication Date
JPS5827959A JPS5827959A (en) 1983-02-18
JPS6237108B2 true JPS6237108B2 (en) 1987-08-11

Family

ID=14931324

Family Applications (1)

Application Number Title Priority Date Filing Date
JP12628181A Granted JPS5827959A (en) 1981-08-11 1981-08-11 Spring steel with superior yielding resistance

Country Status (1)

Country Link
JP (1) JPS5827959A (en)

Families Citing this family (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6089553A (en) * 1983-10-19 1985-05-20 Daido Steel Co Ltd High-strength spring steel and method for manufacturing high-strength springs using the steel
JP2734347B2 (en) * 1986-10-24 1998-03-30 大同特殊鋼株式会社 Manufacturing method of high strength spring steel
JPS63128152A (en) * 1986-11-18 1988-05-31 Kobe Steel Ltd Spring steel having superior settling fatigue resistance
JPH076037B2 (en) * 1986-12-01 1995-01-25 新日本製鐵株式会社 Spring steel with excellent fatigue strength
JP2575711B2 (en) * 1987-06-15 1997-01-29 新日本製鐵株式会社 High strength spring steel for hot forming
JPS648249A (en) * 1987-06-27 1989-01-12 Aichi Steel Works Ltd Spring steel having excellent resistance to permanent set in fatigue and durability
JP2756031B2 (en) * 1990-10-22 1998-05-25 三菱製鋼株式会社 High strength spring steel
CA2057190C (en) * 1991-02-22 1996-04-16 Tsuyoshi Abe High strength spring steel
JPH0578785A (en) * 1991-06-19 1993-03-30 Mitsubishi Steel Mfg Co Ltd High strength spring steel
JP3403913B2 (en) * 1997-03-12 2003-05-06 新日本製鐵株式会社 High strength spring steel
CN102586692A (en) * 2012-04-01 2012-07-18 方大特钢科技股份有限公司 Yttrium composite-treated spring flat steel

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5422771B2 (en) * 1974-01-28 1979-08-09
JPS52127422A (en) * 1976-04-19 1977-10-26 Kobe Steel Ltd Spring steel with high fatigue resistance
JPS57171648A (en) * 1981-04-14 1982-10-22 Kobe Steel Ltd Spring steel

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Publication number Publication date
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