JPS6237109B2 - - Google Patents
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- Publication number
- JPS6237109B2 JPS6237109B2 JP56126283A JP12628381A JPS6237109B2 JP S6237109 B2 JPS6237109 B2 JP S6237109B2 JP 56126283 A JP56126283 A JP 56126283A JP 12628381 A JP12628381 A JP 12628381A JP S6237109 B2 JPS6237109 B2 JP S6237109B2
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- steel
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- spring
- hardenability
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- Springs (AREA)
Description
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。
従来、自動車等の懸架装置に用いられるばね用
鋼としてはSUP6、SUP9が主なものであつた。近
年自動車の軽量化が要請され、懸架装置自体の軽
量化も強く求められるようになつてきた。
これに対して、懸架装置全般にわたつて各種の
手段が試みられているが、その中でもばね設計応
力を上昇させる手段が効果的とされている。この
ように高応力設計にともない、従来の上記ばね用
鋼を素材としばねを製作した場合、へたりが増大
という問題が発生した。特に乗用車に用いた場合
へたりの増大はバンパ高さの低下につながり安全
上の大きな問題となつた。
そこで、各種の研究がなされた結果、ばね用鋼
中のSi含有量を増加させると耐へたり性が向上す
るということを見い出し近時、SUP6よりもさら
にSi含有量が多く、JISG4801に規定されるばね
用鋼中では最も高いSiのSUP7が乗用車懸架ばね
用鋼として広く使用されるに至つている。
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、
Nbを添加し、さらに目的に応じてBあるいはB
とNi、希土類元素のうち1種、あるいはまたTi
を添加することにより、SUP7よりも耐へたり
性、焼入性、靭性がすぐれ、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
を有するばね用鋼を開発したものである。
V、Nbは鋼中において炭化物を形成し、この
バナジウム・カーバイト、ニオブ・カーバイト
(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する。これを急
冷して焼入れするとこれら元素を過飽和に固溶し
たマルテンサイトが得られる。
これを焼もどしするとその過程で微細な合金炭
化物が再析出を始め、これが鋼中において転位の
動きを阻止し、二次硬化を生じ、V、Nbを添加
しないばね用鋼よりも硬さを上昇させ、さらに耐
へたり性を向上させる働きをする。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し得る。
また、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。
本発明鋼においてMn量を低くしたのは、焼入
れに際しての残留オーステナイトの形成を抑える
ことにより鋼の靭性を高めるためである。ばねの
へたりを少なくするために、最近ばねの硬さを上
げる傾向にあるが、ばねの硬さを上げた場合に
は、靭性の低下という新たな問題が生じる。
そこで本発明鋼は、Mn量を低く限定すること
によつてこの新たに生じた問題の解決を図つたも
のである。
このことを明らかにするために後述の0.38%の
Mnを含有するA2鋼と、0.86%のMnを含有する従
来鋼で実質的にSUP7であるB1鋼について実施し
た衝撃試験の結果を第1表に示す。
第1表から明らかなように、本発明鋼である
Mn量の少ないA2鋼は、従来鋼のB1鋼に比べて高
い靭性を有していることがわかる。
The present invention relates to a spring steel with excellent resistance to settling. Conventionally, SUP6 and SUP9 have been the main spring steels used in suspension systems for automobiles and the like. In recent years, there has been a demand for lighter automobiles, and there has also been a strong demand for lighter suspension systems themselves. In response to this problem, various measures have been attempted for suspension systems in general, and among these measures, a measure of increasing the spring design stress is considered to be effective. With this high stress design, when springs are manufactured using the above-mentioned conventional spring steel as a material, a problem arises in that the set-off increases. Particularly when used in passenger cars, increased sag leads to a reduction in bumper height, posing a major safety problem. As a result of various studies, it was discovered that increasing the Si content in spring steel improves the fatigue resistance. SUP7, which has the highest Si among all spring steels, has come to be widely used as a steel for passenger car suspension springs. However, there are strict requirements for reducing the weight of suspension springs, and there has been a strong desire to develop a spring steel with even better fatigue resistance than SUP7. Against this background, the present invention was developed as a result of repeated research by the present inventors, and was developed by adding an appropriate amount of V to high-Si spring steel.
Add Nb and then add B or B depending on the purpose.
and Ni, one of the rare earth elements, or also Ti
By adding , we have developed a spring steel that has better fatigue resistance, hardenability, and toughness than SUP7, and also has the same fatigue resistance as SUP7, which is necessary for spring steel. be. V and Nb form carbides in steel, and vanadium carbide and niobium carbide (hereinafter referred to as alloy carbides) are dissolved in austenite during heating during quenching. When this is rapidly cooled and quenched, martensite containing these elements in a supersaturated solid solution is obtained. When this is tempered, fine alloy carbides begin to re-precipitate in the process, which prevents the movement of dislocations in the steel, causing secondary hardening, making the steel harder than spring steel without the addition of V and Nb. It also works to improve the resistance to fatigue. In addition, alloy carbides that are not dissolved in austenite during heating during quenching can refine austenite crystal grains and prevent them from becoming coarser. Moreover, such fine crystal grains improve the resistance to settling by reducing the amount of movement of dislocations. The reason why the amount of Mn is lowered in the steel of the present invention is to improve the toughness of the steel by suppressing the formation of retained austenite during quenching. Recently, there has been a trend to increase the hardness of springs in order to reduce spring fatigue, but increasing the hardness of springs causes a new problem of reduced toughness. Therefore, the steel of the present invention attempts to solve this new problem by limiting the amount of Mn to a low level. To clarify this, the 0.38%
Table 1 shows the results of impact tests conducted on A2 steel containing Mn and B1 steel, which is a conventional steel containing 0.86% Mn and is substantially SUP7. As is clear from Table 1, it is the steel of the present invention.
It can be seen that A2 steel with a small amount of Mn has higher toughness than B1 steel, which is a conventional steel.
【表】
またB、Ni、希土類元素置は、鋼の焼入性を
高める元素で、特に本発明鋼のような低Mn鋼で
は焼入性が不足する場合があるため、これらの元
素はそれを補う意味で有効に作用するだけでな
く、本発明鋼のさらに大物、厚物のばねへの適用
を可能にするものである。
このことを明らかにするため後述の0.24%のV
と0.11%のNb、0.0022%のBを含有するA4鋼、
0.20%のV、0.13%のNb、0.48%のNi、0.0027%
のBを含有するA6鋼、0.21%のV、0.12%の
Nb、0.0029%のB、0.05%の希土類元素を含有す
るA8鋼と従来鋼のSUP7であるB1鋼について焼入
性を比較した結果を第1表に示す。
第1図から明らかなように、焼入性向上元素の
添加によつてどれも従来鋼以上の焼入性が得られ
ることがわかる。
つぎにTiは鋼中で多くの場合、Nと結合して
窒化物を形成し、熱間圧延段階でオーステナイト
結晶粒を微細化し、オーステナイト化温度に加熱
した時はオーステナイト結晶粒の粗大化を阻止す
る働きを有する。
結晶粒が微細化した組織中では転位の移動量が
少ないことから鋼の耐へたり性を向上することが
できる。
第2図に、Tiを添加した後述のA12鋼と従来鋼
のB1鋼について850〜1100℃の各オーステナイト
化温度に加熱、保持した時のオーステナイト結晶
粒の大きさを示すが、結晶粒の微細化元素の添加
による効果が明瞭に認められる。
本発明鋼の化学組成はC0.50〜0.80%、Si1.50
〜2.50%、Mn0.45%以下を含有し、さらにV0.05
〜0.50%、Nb0.11〜0.50%を含有したもので、使
用目的によつてはさらにB0.0005〜0.0100%ある
いはB0.0005〜0.0100%とNi0.20〜0.60%、希土類
元素0.10%以下のうち1種を含有し、あるいはま
たTi0.02〜0.10%のうち1種を含有し、残り実質
的にFeよりなるものである。
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0.45%以下としたのは、Mn量を0.45%
以下に限定することにより残留オーステナイトの
形成を低く抑えることにより、鋼に靭性を付与す
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の含有量を0.05〜
0.50%としたのは、0.05%以下では上記の効果が
十分に得られないためであり、Nbの含有量を
0.11〜0.50%としたのは、下限以下では上記の効
果が十分に得られないためである。
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。
また鋼の焼入性を高める元素であるB、Ni、
希土類元素の量をそれぞれB0.0005〜0.0100%、
Ni0.20〜0.60%、希土類元素0.10%以下としたの
は、Bについては、0.0005%以下では焼入性向上
に十分でないからであり、0.0100%を越えて含有
させても効果が飽和し、かつ、B化合物の形成に
より熱間脆性を招く恐れがあるためである。
またNiについては、0.20%以下では焼入性の向
上、及び靭性の向上効果が十分に得られないため
であり、0.60%を超えて含有させても効果の向上
が少ないためである。
希土類元素量を0.30%以下としたのは、それ以
上含有させると結晶粒が粗大化する恐れがあるた
めである。
また結晶粒を微細化して耐へたり性を向上させ
るTiの含有量を0.02〜0.10%としたのは、それ以
下では窒化物の分布が疎らで、結晶粒の微細化に
寄与しないからであり、0.10%を越えて含有させ
ると、熱間圧延時に割れを発生したり、非金属介
在物として鋼の靭性を劣化させる恐れがあるため
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2表は、これらの供試鋼の化学成分を示すも
のである。[Table] In addition, B, Ni, and rare earth elements are elements that improve the hardenability of steel.In particular, low Mn steel such as the steel of the present invention may have insufficient hardenability, so these elements are This not only works effectively in the sense of supplementing the above, but also enables the steel of the present invention to be applied to even larger and thicker springs. In order to clarify this, the 0.24% V described below
A4 steel containing 0.11% Nb and 0.0022% B,
0.20% V, 0.13% Nb, 0.48% Ni, 0.0027%
A6 steel containing B, 0.21% V, 0.12%
Table 1 shows the results of comparing the hardenability of A8 steel containing Nb, 0.0029% B, and 0.05% rare earth elements and B1 steel, which is a conventional steel SUP7. As is clear from FIG. 1, it can be seen that the addition of hardenability-improving elements makes it possible to obtain hardenability higher than that of conventional steels. Next, Ti often combines with N to form nitrides in steel, which refines austenite grains during hot rolling and prevents austenite grains from coarsening when heated to the austenitizing temperature. It has the function of Since the amount of movement of dislocations in a structure with finer grains is smaller, the fatigue resistance of the steel can be improved. Figure 2 shows the size of austenite crystal grains when heated and held at each austenitizing temperature of 850 to 1100°C for A12 steel with Ti added and conventional steel B1, which will be described later. The effect of the addition of chemical elements is clearly recognized. The chemical composition of the steel of the present invention is C0.50-0.80%, Si1.50
Contains ~2.50%, Mn0.45% or less, and V0.05
~0.50%, Nb0.11~0.50%, and depending on the purpose of use, it may further contain B0.0005~0.0100% or B0.0005~0.0100%, Ni0.20~0.60%, and rare earth elements 0.10% or less. It contains one of these, or it also contains one of 0.02 to 0.10% Ti, and the rest is essentially Fe. 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 why the Mn amount is 0.45% or less is that the Mn amount is 0.45%.
This is to provide toughness to the steel by suppressing the formation of retained austenite by limiting it to the following. Both V and Nb are elements that improve the sag resistance in the steel of the present invention. The content of V, which plays this role, is 0.05~
The reason why the Nb content was set at 0.50% is that the above effects cannot be obtained sufficiently below 0.05%.
The reason for setting it to 0.11 to 0.50% is that the above effects cannot be sufficiently obtained below the lower limit. Even if the content exceeds 0.50%, the effect is saturated, and the amount of alloy carbides that are not dissolved in austenite increases, forming large lumps that reduce the fatigue strength of steel by acting like nonmetallic inclusions. This is because there is fear. 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. In addition, B, Ni, which are elements that improve the hardenability of steel,
The amount of rare earth elements is B0.0005~0.0100%, respectively.
The reason for setting Ni to 0.20 to 0.60% and rare earth elements to 0.10% or less is because B is not sufficient to improve hardenability when it is contained at 0.0005% or less, and even if it is contained in excess of 0.0100%, the effect is saturated. This is also because the formation of the B compound may cause hot embrittlement. Regarding Ni, if it is less than 0.20%, the effect of improving hardenability and toughness cannot be sufficiently obtained, and if it is contained in an amount exceeding 0.60%, the effect is not improved much. The reason why the amount of rare earth elements is set to 0.30% or less is that if it is contained more than that, the crystal grains may become coarse. In addition, the content of Ti, which refines crystal grains and improves resistance to settling, was set at 0.02 to 0.10% because if it is less than that, the distribution of nitrides will be sparse and will not contribute to grain refinement. This is because if the content exceeds 0.10%, it may cause cracks during hot rolling or deteriorate the toughness of the steel as nonmetallic inclusions. Next, the characteristics of the steel of the present invention will be clarified through examples in comparison with conventional steel. Table 2 shows the chemical composition of these test steels.
【表】
第2表においてA2鋼は第1発明鋼で、A4鋼は
第2発明鋼、A6、A8鋼は第3発明鋼、A12鋼は
第4発明鋼で、B1鋼は従来鋼でSUP7である。
供試鋼はすべて鋳造後圧延比50以上で熱間圧延
を施し、次に述べるへたり試験に供した。
へたり試験を施行するに当たつては、第3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=115Kg/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 2, A2 steel is the first invention steel, A4 steel is the second invention steel, A6 and A8 steel are the third invention steel, A12 steel is the fourth invention steel, and B1 steel is the conventional steel with SUP7 It is. All of the sample steels were hot-rolled at a rolling ratio of 50 or higher after casting, and were subjected to the sag test described below. To carry out the fatigue test, a coil spring with the specifications shown in Table 3 is formed, quenched and tempered to a final hardness of HRC45 to 55, and then A setting test piece was prepared by setting the wire so that the shear stress τ=115 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 ,
The amount of fatigue of the coil spring was measured after 96 hours (hereinafter referred to as long-term loading).
【表】
しかし、焼入性向上元素を添加したA4、A6、
A8鋼については、第4表に示す諸元を有するト
ーシヨン・バーを作成し、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τ
=110Kgf/mm2の応力でセツチングを施し、その
後、τ=100Kgf/mm2の応力を96時間負荷し、そ
の間に発生したへたり量を測定した。[Table] However, A4, A6, which added hardenability improving elements,
For A8 steel, we created a torsion bar with the specifications shown in Table 4, and the final hardness was HRC45~
After quenching and tempering so that it becomes 55, τ
Setting was performed with a stress of =110 Kgf/mm 2 , and then a stress of τ = 100 Kgf/mm 2 was applied for 96 hours, and the amount of settling that occurred during that time was measured.
【表】
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とを測定し、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/πd3△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
定まる定数)
また、トーシヨン・バーからのへたり量は、ね
じり角度の減少量△θからYR=△θ・d/2lに
従つて残留剪断歪量に変換して求めた。
d:線径(mm)
l:有効長さ(mm)
そして、上記試験片の硬さに対するへたり量を
第3〜6図に示した。第3〜6図より明らかなよ
うに本発明鋼はいずれも従来鋼であるB1鋼に比
べすぐれた耐へたり性を有していることが認めら
れる。
また本発明鋼のA2およびB1鋼については前記
と同じ諸元を有するコイルばねで、またA4、
A6、A8については前記のトーシヨン・バーを用
いて10〜110Kgf/mm2の応力を繰り返し負荷して
疲労試験を実施したが、いずれの試料も20万回繰
り返しても折損しなかつた。
上述の如く、本発明鋼は高Siばね用鋼に、V、
Nbなどの析出強化元素、B、Ni、希土類元素等
の焼入性向上元素、またさらにはAl、Tiのよう
な結晶粒の微細化元素を添加することにより、従
来の高Siばね用鋼の優れた耐へたり性をさらに改
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] The amount of set is the load required to compress the coil spring to a certain height before applying the long-term load mentioned above.
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, the amount of setback from the torsion bar was determined by converting the amount of decrease in the torsion angle Δθ into the amount of residual shear strain according to YR=Δθ·d/2l. d: Wire diameter (mm) l: Effective length (mm) The amount of set in relation to the hardness of the test piece is shown in Figures 3 to 6. As is clear from FIGS. 3 to 6, it is recognized that all of the steels of the present invention have superior sag resistance compared to B1 steel, which is a conventional steel. In addition, A2 and B1 steels of the present invention are coil springs having the same specifications as above, and A4,
A fatigue test was conducted on A6 and A8 by repeatedly applying a stress of 10 to 110 Kgf/mm 2 using the above-mentioned torsion bar, but none of the samples broke even after 200,000 repetitions. As mentioned above, the steel of the present invention is a high-Si spring steel with V,
By adding precipitation-strengthening elements such as Nb, hardenability-improving elements such as B, Ni, and rare earth elements, and grain-refining elements such as Al and Ti, conventional high-Si spring steels can be improved. This product has succeeded in further improving its excellent fatigue resistance, and the fatigue resistance required for spring steel is also comparable to that of conventional steel, and is particularly high as a steel for passenger car suspension springs. It is practical.
第1図は、特に焼入性向上元素を添加した本発
明鋼と従来鋼について焼入性を比較した線図で、
第2図は、本発明鋼と従来鋼を850〜1100℃の各
オーステナイト化温度で加熱保持した時のオース
テナイト結晶粒度を示した線図、第3〜5図は、
本発明鋼と従来鋼を焼入れ・焼もどし処理後、硬
さをHRC45〜55にした時の試験片のへたり量を
示した線図である。
Figure 1 is a diagram comparing the hardenability of the present invention steel with added hardenability-improving elements and conventional steel.
Figure 2 is a diagram showing the austenite grain size when the present invention steel and conventional steel are heated and held at various austenitizing temperatures of 850 to 1100°C, and Figures 3 to 5 are
FIG. 2 is a diagram showing the amount of settling of test pieces when the steel of the present invention and the conventional steel are hardened to HRC45 to HRC55 after being quenched and tempered.
Claims (1)
%、Mn0.45%以下と、V0.05〜0.50%、Nb0.11〜
0.50%を含有し、残り実質的にFeからなること
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
%、Mn0.45%以下と、V0.05〜0.50%、Nb0.11〜
0.50%を含有し、さらにB0.0005〜0.0100%を含
有し、残り実質的にFeからなることを特徴とす
る耐へたり性の優れたばね用鋼。 3 重量比にしてC0.50〜0.80%、Si1.50〜2.50
%、Mn0.45%以下と、V0.05〜0.50%、Nb0.11〜
0.50%を含有し、さらにB0.0005〜0.0100%と、
Ni0.20〜0.60%、希土類元素0.10%以下のうち1
種を含有し、残り実質的にFeからなることを特
徴とする耐へたり性の優れたばね用鋼。 4 重量比にしてC0.50〜0.80%、Si1.50〜2.50
%、Mn0.45%以下と、V0.05〜0.50%、Nb0.11〜
0.50%を含有し、さらにTi0.020〜0.10%を含有
し、残り実質的にFeから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
%, Mn0.45% or less, V0.05~0.50%, Nb0.11~
A spring steel with excellent fatigue resistance characterized by containing 0.50% Fe with the remainder essentially consisting of Fe. 2 C0.50~0.80%, Si1.50~2.50 by weight
%, Mn0.45% or less, V0.05~0.50%, Nb0.11~
A spring steel with excellent fatigue resistance, characterized in that it contains 0.50% B, further contains 0.0005 to 0.0100% B, and the remainder substantially consists of Fe. 3 C0.50~0.80%, Si1.50~2.50 by weight
%, Mn0.45% or less, V0.05~0.50%, Nb0.11~
Contains 0.50% and further B0.0005 to 0.0100%,
1 of Ni 0.20-0.60%, rare earth elements 0.10% or less
A spring steel with excellent fatigue resistance, which is characterized by containing seeds and the remainder being essentially Fe. 4 C0.50~0.80%, Si1.50~2.50 by weight
%, Mn0.45% or less, V0.05~0.50%, Nb0.11~
A spring steel with excellent fatigue resistance, characterized by containing 0.50% of Ti, further containing 0.020 to 0.10% of Ti, and the remainder substantially consisting of Fe.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12628381A JPS5827957A (en) | 1981-08-11 | 1981-08-11 | Spring steel with excellent fatigue resistance |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP12628381A JPS5827957A (en) | 1981-08-11 | 1981-08-11 | Spring steel with excellent fatigue resistance |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5827957A JPS5827957A (en) | 1983-02-18 |
| JPS6237109B2 true JPS6237109B2 (en) | 1987-08-11 |
Family
ID=14931376
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP12628381A Granted JPS5827957A (en) | 1981-08-11 | 1981-08-11 | Spring steel with excellent fatigue resistance |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5827957A (en) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62198007A (en) * | 1986-02-25 | 1987-09-01 | 松下冷機株式会社 | Wiring harness |
| JPH01267910A (en) * | 1988-03-18 | 1989-10-25 | Dsg Schrumpfschlauch Gmbh | Method and apparatus for providing water-tight sealing of multiple cable strand longitudinally |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2505235B2 (en) * | 1988-01-18 | 1996-06-05 | 新日本製鐵株式会社 | High strength spring steel |
| JP2683960B2 (en) * | 1991-02-22 | 1997-12-03 | 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 |
| JP2932943B2 (en) * | 1993-11-04 | 1999-08-09 | 株式会社神戸製鋼所 | High corrosion resistance and high strength steel for springs |
| KR960005230B1 (en) * | 1993-12-29 | 1996-04-23 | 포항종합제철주식회사 | Manufacturing method of high strength high toughness spring steel |
| CN110592319B (en) * | 2019-09-10 | 2020-12-01 | 中国科学院金属研究所 | Rare earth microalloyed steel and control method |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS57171648A (en) * | 1981-04-14 | 1982-10-22 | Kobe Steel Ltd | Spring steel |
-
1981
- 1981-08-11 JP JP12628381A patent/JPS5827957A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62198007A (en) * | 1986-02-25 | 1987-09-01 | 松下冷機株式会社 | Wiring harness |
| JPH01267910A (en) * | 1988-03-18 | 1989-10-25 | Dsg Schrumpfschlauch Gmbh | Method and apparatus for providing water-tight sealing of multiple cable strand longitudinally |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5827957A (en) | 1983-02-18 |
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