JPS625215B2 - - Google Patents
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- Publication number
- JPS625215B2 JPS625215B2 JP21916682A JP21916682A JPS625215B2 JP S625215 B2 JPS625215 B2 JP S625215B2 JP 21916682 A JP21916682 A JP 21916682A JP 21916682 A JP21916682 A JP 21916682A JP S625215 B2 JPS625215 B2 JP S625215B2
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- Prior art keywords
- less
- rolling
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- steel
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Classifications
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Heat Treatment Of Steel (AREA)
Description
本発明は溶接性と低温靭性の優れた高張力鋼の
製造方法に関するものであり、特に本発明は溶接
をともない低温靭性が要求される高張力厚鋼板た
とえば氷海域構造用鋼板、造船用高張力鋼板、ブ
タン、プロパン向けタンクなどの圧力容器用鋼
板、寒冷地向けラインパイプ用鋼板等を調質を施
さずに製造する方法に関するものである。
従来溶接をともなう低温靭性の優れた高張力鋼
板はNorma処理、QT処理によつて製造されてき
ているが熱処理費等の高騰により製造コストが高
くなるという欠点がある。また熱処理を施さない
いわゆる非調質で高張力化、高靭性化を図る製造
方法としては制御圧延(以下CRと称す)による
方法があるが、CR材でNorma材、QT材に代わる
程の高張力化を図るためには、CRの仕上げ圧延
温度を下げる必要があるため、圧延能率が著しく
低下するばかりか、得られた鋼板のシヤルピー衝
撃破面にはセパレーシヨンが発生し、ユーザーか
ら嫌われ適用鋼種の拡大がむずかしいという欠点
がある。
CRによる上記欠点を改善した低温域までのCR
を必要としないで高張力化を図る製造方法として
圧延後の加速冷却をなす方法があるが、この加速
冷却による方法では、第1図に示すC0.06%,
Mn1.4%、Geq0.29%を含む鋼板について行つた
冷却速度と強度(以下TSと称す)ならびに降伏
強度(以下YSと称す)との関係からわかるよう
に、冷却速度を速くすることによつてTSは容易
に上昇させることはできるが、一方YSは冷却速
度が比較的遅いときは降下し、逆に冷却速度が速
くなると上昇するが、その上昇量は非常に少ない
という欠点があり、加速冷却によつて製造された
鋼は、YS不足のためNorma材、QT材の代替鋼と
なり得る鋼種は限られ、いまだ十分満足されてい
ない。
本発明は、上記従来の製造方法においてみられ
る欠点を除いた溶接性と低温靭性の優れた高張力
鋼を調質処理を施さずに生産性の向上と低廉な製
造方法を提供することを目的とし特許請求の範囲
記載の方法を提供することにより前記目的を達成
することができる。
次に本発明を詳細に説明する。
本発明者等は、熱処理を施さずにYSを上昇さ
せる方法を検討した結果、圧延後ただちに加速冷
却をなし、圧延鋼板が500℃未満の温度において
加速冷却を停止し、500℃未満から200℃以上の温
度域で圧下率0.5%から20%未満の範囲内の軽圧
下を施すことによりYSが著しく上昇することを
新規に知見した。すなわちYSの急上昇は加速冷
却後再び軽圧下を施すことにより得ることができ
る。
ところでこの軽圧下を施すことにより、TSは
YSの上昇率には及ばないながら、相当上昇する
という利点があり、さらにシヤルピー衝撃破面に
はセパレーシヨンが発生しないという利点もある
が、一方この軽圧下は靭性を悪化させるという欠
点が生じ、低温靭性を要求する鋼種には適用が難
しいという問題が生起した。
本発明者らは低温靭性を改善する方法について
日夜研鑽の結果、本発明の特許請求の範囲記載の
成分組成にしめすTiを含有させることにより、
スラブ加熱においてγ粒の細粒維持ができるの
で、CRを施し引続き加速冷却をなした鋼板の組
織は微細化されておるので、加速冷却停止後に軽
圧下を施しても靭性の劣化が少なくして、YS、
TSが上昇することをさらに知見して本発明に想
到した。
次に本発明を実験データについて説明する。
第2図はC0.06〜0.07%,Mn1.4%を含有する
Ti含有鋼(すなわち本発明鋼、〇印)と同じく
Ti無含有鋼(すなわち比較鋼、△印)とのYS、
TSおよび遷移温度(以下VTrsと称す)の関係を
400℃において圧下率の変化により比較したもの
である。同図によればTi含有鋼はTi無含有鋼に
くらべTS、YSに悪影響を及ぼすことなくvTrsを
大幅に改善できることがわかる。
すなわちTi含有鋼にCRを施し、ただちに加速
冷却をなすことによりTSが上昇し、引き続き加
速冷却を停止したのち軽圧下を施すことにより
YSが上昇するので熱処理を施すことなく高い
TS、YSを得ることができ、さらに低温靭性も非
常に高くなるのでNorma材、QT材より低いか多
くとも同量の炭素当量(以下Ceqと称す)で高張
力を得ることができる。
次に本発明の成分組成を限定する理由を説明す
る。
Cは0.005%未満では鋼板の強度が低下し、ま
た溶接熱影響部(以下HAZと称す)の軟化が大
きくなり、一方0.15%を越えると母材の靭性が劣
化するとともに溶接部の硬化、耐割れ性の劣化が
著しくなるので、Cは0.005〜0.15%の範囲内に
する必要がある。
Siは鋼精錬時に脱酸上必然的に含有される元素
であるが、0.1%未満では母材靭性が劣化し、一
方0.5%を越えると鋼の清浄度が劣化し靭性が低
下するので、Siは0.1〜0.5%の範囲内にする必要
がある。
Mnは0.8%未満では鋼板の強度および靭性が低
下し、さらにHAZの軟化が大きくなり、一方2.0
%を越えるとHAZの靭性が劣化するので、Mnは
0.8〜2.0%の範囲内にする必要がある。
Alは鋼の脱酸上最低0.005%のAlが固溶するよ
うに添加することが必要であり、一方0.08%を越
えるとHAZの靭性のみならず溶接金属の靭性も
著しく劣化するので、Alは0.005〜0.08%の範囲
内にする必要がある。
Sは0.008%を越えるとC方向の吸収エネルギ
ーが著しく低下するので、Sは0.008%以下にす
る必要がある。
TiはTiN析出物となりγ粒を微細化させフエラ
イト、ベイナイト粒を微細にする効果があるが、
0.003%未満ではTiN析出物量が不足し細粒効果
がなく、一方0.04%を越えるとTiN析出物が過剰
となり靭性が劣化するので、Tiは0.003〜0.04%
の範囲内にする必要がある。
Nは溶接部靭性の劣化を防止するために限定す
る必要がある。すなわちHAZ靭性のためには固
溶Nが少ない程好ましく、また溶接時に溶接金属
へNが流入し溶接金属の靭性をも劣化させるが
0.0010%以下では細粒に必要なTiN析出物量が不
足し、一方0.010%以上ではTiN析出物量が過剰
もしくは固溶Nが残在し、いずれにおいても溶接
部の靭性を劣化させるので、Nは0.0010%を越え
0.010%未満の範囲内にする必要があり、更にTi
含有量との関係においてN量を下式に限定したの
は
(Ti%/3.4−0.0020%)
<N<(Ti%/3.4+0.0020%)
固溶Nを減少させるためのものである。すなわち
NとTiの関係で両元素が過不足なくTiN析出物と
なるためには、N含有量は理論上ではTi%/3.4と
な
るが、N含有量をTi%/3.4に調整することは事実
上
不可能であるので、Nは実操業上から(Ti%/3.4
−
0.0020%)を越え(Ti%/3.4+0.0020%)未満の
範囲
内にする。
以上が本発明において使用される鋼スラブの基
本成分であり、さらに必要によりNi,Mo,Cu,
V,Cr,Ca,RENのうちから選ばれる何れか少
なくとも1種を添加含有させることができ、それ
ぞれの元素の適正な含有によつて後述するように
特有な効果が付加される。
NiはHAZの硬化性および靭性に悪い影響を与
えることなく母材の強度、靭性を向上させるが、
0.5%を越えて添加含有させると製造コストの上
昇を招き、また本発明の目的ならびに効果を達成
するために必要ではないので、Niは0.5%以下に
する。
CuはNiとほぼ同様の効果があるだけでなく、
耐食性も向上させるが、0.5%を越えると熱間圧
延中にクラツクが発生しやすくなり、鋼板の表面
性状が劣化するので、Cuは0.5%以下にする必要
がある。
Moは圧延時のγ粒を整粒となし、なおかつ微
細なベイナイトを生成するので強度、靭性を向上
させるが、この発明の目的を達成するには0.5%
を越えて添加含有させる必要はなく、それ以上は
製造コストの上昇を招くので、Moは0.5%以下に
する。
Crは鋼板の母材強度と継手部強度確保のため
に添加含有させるが0.5%を越えると母材の靭性
ばかりか溶接部靭性も劣化するので、Crは0.5%
以下にする必要がある。
Vは鋼板の母材強度と靭性向上、継手部強度確
保のために添加含有させるが、0.01%未満ではそ
の効果がなく、一方0.10%を越えると母材及び
HAZの靭性を著しく劣化させるので、Vは0.01〜
0.10%の範囲内にする必要がある。
Caは0.002%未満ではMnSの形態制御に不十分
でC方向の靭性向上に効果がなく、一方0.010%
を越えると鋼の清浄度が悪くなり内部欠陥の原因
となるので、Caは0.002〜0.010%の範囲内にする
必要がある。
REMは0.005%未満ではMnSの形態制御に不十
分で鋼板のC方向の靭性向上に有効でなく、一方
0.010%を越えると鋼の清浄度が悪くなり、また
アーク溶接面でも不利であるので、REMは0.005
〜0.010%の範囲内にする必要がある。
次に本発明の製造条件を限定する理由を説明す
る。
鋼片を加熱後、Ar3+70℃からAr3までの未再
結晶γ域で50〜90%の圧下を施す。圧延仕上げ温
度をAr3+70℃からAr3まで限定する理由は、こ
の温度域で圧延を施すことによる細粒化機構はオ
ーステナイト粒内にフエライト核となる変形帯を
多く生成させることにあるが、Ar3+70℃を越え
る温度域だけの圧延ではオーステナイト粒内に変
形帯が生成されず。フエライト粒を十分に微細化
できないので微細粒による高い靭性を得ることが
できず、一方Ar3点未満の温度域で圧延を施すと
シヤルピー衝撃破面にセパレーシヨンが生じるの
で、圧延温度域はAr3+70℃〜Ar3の範囲内にす
る必要がある。更に上記温度域における圧延にお
いて圧下率を50〜90%に限定する理由は、圧下率
が50%未満ではオーステナイト粒内に変形帯の生
成が不十分なため、後述する圧延後の加速冷却を
施すことによりフエライト粒は細粒化せずに塊状
のベイナイトが生成するため、靭性が著しく劣化
する。一方、90%を越える圧下率で圧延を施すと
導入される変形帯が飽和するため、その後の加速
冷却を施しても靭性の向上効果が小さくなるの
で、未再結晶γ域での圧下率は50〜90%の範囲内
にする必要がある。
圧延後直ちに2〜40℃/secの冷却速度で500℃
未満の温度域まで加速冷却を施す理由は(1)γ→α
変態後のフエライト粒の成長を抑え、靭性を向上
させること、(2)パーライト組織となる変態域をベ
イナイト組織あるいは島状マルテンサイト組織に
変態させることにより主としてTSを上昇させる
ことにあるが、冷却速度が2℃/sec未満ではベ
イナイト組織等の生成効果がなく、一方40℃/
secを越えると塊状のマルテンサイト組織が生成
して著しく靭性を劣化させるので、冷却速度は2
〜40℃/secの範囲内にする必要がある。また冷
却停止温度は500℃以上ではベイナイトやマルテ
ンサイト組織の生成量が不足しTSの上昇が空冷
材に比べ5Kgf/mm2以下となり、本発明の目的と
するQT鋼の代替とならないので、冷却停止温度
は500℃未満にする必要がある。
冷却停止後500℃未満から200℃以上の温度域に
おいて0.5%から20%未満の圧下率で軽圧下を施
す理由は、主としてYSの上昇を目的とするもの
であり、500℃以上の温度域による軽圧下ではYS
の上昇量が少なく、一方200℃より低い温度域で
軽圧下を施すと水素の除去が十分出来ないため水
素欠陥が起るので、軽圧下を施す温度域は500℃
未満から200℃以上の範囲内にする必要がある。
軽圧下の圧下率は第2図に示されているように
0.5%未満ではYSの上昇に顕著な効果がなく、一
方20%以上ではシヤルピー衝撃破面にセパレーシ
ヨンが発生するので、500℃未満から200℃以上の
温度域による圧下率は0.5%から20%未満の範囲
内にする必要がある。
200℃未満の温度域において空冷ないし徐冷を
なすのは水素の除去を容易にし水素欠陥を防止す
るためである。
次に本発明を実施例について説明する。
実施例
第1表に成分組成を示す供試鋼種を第2表に示
す圧延―冷却条件により処理した鋼板の機械的性
質を同表に示す。
The present invention relates to a method for manufacturing high-strength steel with excellent weldability and low-temperature toughness, and in particular, the present invention relates to a method for manufacturing high-strength steel with excellent weldability and low-temperature toughness. The present invention relates to a method for manufacturing steel plates, steel plates for pressure vessels such as tanks for butane and propane, steel plates for line pipes for cold regions, etc., without thermal refining. Conventionally, high-strength steel sheets with excellent low-temperature toughness that involve welding have been manufactured by Norma treatment and QT treatment, but they have the disadvantage of increasing manufacturing costs due to the rise in heat treatment costs. Controlled rolling (hereinafter referred to as CR) is a manufacturing method that uses so-called non-thermal treatment that does not involve heat treatment to achieve high tensile strength and high toughness. In order to increase the tension, it is necessary to lower the finish rolling temperature of CR, which not only significantly reduces rolling efficiency but also causes separation on the shear py impact fracture surface of the resulting steel plate, which is disliked by users. The drawback is that it is difficult to expand the range of applicable steel types. CR that improves the above drawbacks of CR up to low temperature range
There is a method of accelerated cooling after rolling that achieves high tensile strength without requiring C0.06%, as shown in Figure 1.
As can be seen from the relationship between cooling rate and strength (hereinafter referred to as TS) and yield strength (hereinafter referred to as YS) for a steel plate containing 1.4% Mn and 0.29% Geq, increasing the cooling rate Therefore, TS can be easily increased, but YS decreases when the cooling rate is relatively slow, and conversely increases when the cooling rate increases, but the disadvantage is that the amount of increase is very small. Due to the lack of YS in steel produced by cooling, there are only a limited number of steel types that can be used as substitutes for Norma and QT materials, and they are still not fully satisfied. The purpose of the present invention is to provide a method for manufacturing high-strength steel with excellent weldability and low-temperature toughness, which eliminates the drawbacks seen in the conventional manufacturing methods, without heat treatment, and which improves productivity and is inexpensive. The above object can be achieved by providing the method as described in the claims. Next, the present invention will be explained in detail. The present inventors investigated a method of increasing YS without heat treatment, and found that accelerated cooling is performed immediately after rolling, and accelerated cooling is stopped when the rolled steel sheet reaches a temperature of less than 500°C. We have newly discovered that YS increases significantly by applying light reduction within the range of 0.5% to less than 20% in the above temperature range. In other words, a rapid increase in YS can be obtained by applying light pressure reduction again after accelerated cooling. By the way, by applying this light reduction, the TS becomes
Although it does not reach the rate of increase of YS, it has the advantage of increasing considerably, and also has the advantage that separation does not occur on the sharpey impact fracture surface, but on the other hand, this light reduction has the disadvantage of worsening toughness. A problem arose in that it was difficult to apply to steel types that required low-temperature toughness. The present inventors have studied day and night on a method for improving low-temperature toughness, and as a result, by incorporating Ti into the component composition described in the claims of the present invention,
Since the fine γ grains can be maintained during slab heating, the structure of the steel sheet that has been subjected to CR and then accelerated cooling is refined, so even if light reduction is applied after the accelerated cooling has stopped, there is less deterioration in toughness. , Y.S.
The present invention was conceived after further discovering that TS increases. Next, the present invention will be explained using experimental data. Figure 2 contains 0.06-0.07% C and 1.4% Mn.
Same as Ti-containing steel (i.e. steel of the present invention, marked with ○)
YS with Ti-free steel (i.e. comparative steel, marked △),
The relationship between TS and transition temperature (hereinafter referred to as VTrs) is
A comparison was made by changing the rolling reduction rate at 400°C. According to the figure, it can be seen that Ti-containing steel can significantly improve vTrs without adversely affecting TS and YS compared to Ti-free steel. In other words, by applying CR to Ti-containing steel and immediately performing accelerated cooling, TS increases, and by subsequently stopping accelerated cooling and applying light reduction.
YS increases, so it is high without heat treatment.
TS and YS can be obtained, and the low-temperature toughness is also very high, so high tensile strength can be obtained with a carbon equivalent (hereinafter referred to as Ceq) lower than or at most the same amount as Norma and QT materials. Next, the reason for limiting the component composition of the present invention will be explained. If C is less than 0.005%, the strength of the steel plate will decrease and the weld heat affected zone (hereinafter referred to as HAZ) will become significantly softened, while if it exceeds 0.15%, the toughness of the base metal will deteriorate, and the weld will harden and become resistant. Since deterioration of crackability becomes significant, C needs to be within the range of 0.005 to 0.15%. Si is an element that is inevitably included for deoxidation during steel refining, but if it is less than 0.1%, the toughness of the base material will deteriorate, while if it exceeds 0.5%, the cleanliness of the steel will deteriorate and the toughness will decrease. must be within the range of 0.1-0.5%. If Mn is less than 0.8%, the strength and toughness of the steel plate will decrease, and the softening of the HAZ will increase;
%, the toughness of HAZ deteriorates, so Mn
It must be within the range of 0.8 to 2.0%. Al needs to be added in such a way that at least 0.005% of Al becomes a solid solution for deoxidizing the steel.On the other hand, if it exceeds 0.08%, not only the toughness of the HAZ but also the toughness of the weld metal will deteriorate significantly. Must be within the range of 0.005-0.08%. If S exceeds 0.008%, the absorbed energy in the C direction will drop significantly, so S must be kept at 0.008% or less. Ti forms TiN precipitates and has the effect of refining γ grains and refining ferrite and bainite grains.
If it is less than 0.003%, the amount of TiN precipitates will be insufficient and there will be no fine grain effect, while if it exceeds 0.04%, the amount of TiN precipitates will be excessive and the toughness will deteriorate, so Ti is 0.003 to 0.04%.
Must be within the range. N needs to be limited in order to prevent deterioration of the weld toughness. In other words, for HAZ toughness, it is better to have as little solid solution N as possible, and N flows into the weld metal during welding, which also deteriorates the toughness of the weld metal.
If it is less than 0.0010%, the amount of TiN precipitates required for fine grains will be insufficient, while if it is more than 0.010%, the amount of TiN precipitates will be excessive or solid solution N will remain, and in either case, the toughness of the weld will deteriorate, so N is 0.0010. over %
It must be within the range of less than 0.010%, and Ti
In relation to the content, the N amount is limited to the following formula: (Ti%/3.4-0.0020%) <N< (Ti%/3.4+0.0020%) This is to reduce solid solution N. It is. In other words, in order to form TiN precipitates with just the right amount of both elements in the relationship between N and Ti, the N content should theoretically be Ti%/3.4, but the N content should be Ti%/3.4. Since it is virtually impossible to adjust, N is set to (Ti%/3.4
- 0.0020%) and less than (Ti%/3.4 + 0.0020%). The above are the basic components of the steel slab used in the present invention, and if necessary, Ni, Mo, Cu, etc.
At least one selected from V, Cr, Ca, and REN can be added, and proper inclusion of each element adds a unique effect as described later. Ni improves the strength and toughness of the base metal without adversely affecting the hardenability and toughness of HAZ.
If Ni is added in an amount exceeding 0.5%, it will increase the manufacturing cost and is not necessary to achieve the objects and effects of the present invention, so the content of Ni should be 0.5% or less. Cu not only has almost the same effect as Ni, but also
It also improves corrosion resistance, but if it exceeds 0.5%, cracks are likely to occur during hot rolling and the surface quality of the steel sheet deteriorates, so it is necessary to keep Cu at 0.5% or less. Mo makes the γ grains regular during rolling and also produces fine bainite, which improves strength and toughness, but in order to achieve the purpose of this invention, 0.5% Mo
It is not necessary to add more than 0.5%, and any more will increase the manufacturing cost, so the content of Mo should be 0.5% or less. Cr is added to ensure the strength of the base metal of the steel plate and the strength of the joint, but if it exceeds 0.5%, not only the toughness of the base metal but also the toughness of the weld will deteriorate, so Cr should be added at 0.5%.
It is necessary to do the following. V is added to improve the strength and toughness of the base material of steel sheets and ensure joint strength, but if it is less than 0.01%, it has no effect, while if it exceeds 0.10%, it will damage the base material and the strength of the joint.
Since it significantly deteriorates the toughness of HAZ, V is 0.01~
Must be within 0.10%. If Ca is less than 0.002%, it is insufficient to control the morphology of MnS and has no effect on improving the toughness in the C direction;
If it exceeds Ca, the cleanliness of the steel will deteriorate and cause internal defects, so Ca must be within the range of 0.002 to 0.010%. If REM is less than 0.005%, it is insufficient to control the morphology of MnS and is not effective in improving the toughness of the steel plate in the C direction.
If it exceeds 0.010%, the cleanliness of the steel will deteriorate and it will also be disadvantageous for arc welding, so REM is 0.005%.
Must be within the range of ~0.010%. Next, the reason for limiting the manufacturing conditions of the present invention will be explained. After heating the steel slab, it is rolled down by 50 to 90% in the non-recrystallized γ range from Ar 3 +70°C to Ar 3 . The reason why the finishing rolling temperature is limited from Ar 3 +70℃ to Ar 3 is that the grain refining mechanism caused by rolling in this temperature range generates many deformed bands that become ferrite nuclei within the austenite grains. Ar 3 Rolling only in the temperature range exceeding +70°C does not produce deformation bands within the austenite grains. Since the ferrite grains cannot be made sufficiently fine, it is not possible to obtain high toughness due to the fine grains.On the other hand, if rolling is performed in a temperature range below the Ar 3 point, separation will occur on the shear pie impact fracture surface, so the rolling temperature range is 3 Must be within the range of +70℃~ Ar3 . Furthermore, the reason why the rolling reduction rate is limited to 50 to 90% during rolling in the above temperature range is that if the rolling reduction rate is less than 50%, the generation of deformation bands in the austenite grains is insufficient, so accelerated cooling after rolling, which will be described later, is performed. As a result, the ferrite grains do not become finer, but massive bainite is produced, resulting in a significant deterioration in toughness. On the other hand, when rolling is carried out at a reduction rate exceeding 90%, the introduced deformation band becomes saturated, and even if subsequent accelerated cooling is performed, the effect of improving toughness becomes small, so the reduction rate in the non-recrystallized γ region is It should be within the range of 50-90%. Immediately after rolling, heat to 500℃ at a cooling rate of 2 to 40℃/sec.
The reason for performing accelerated cooling to the temperature range below is (1) γ→α
(2) Mainly to increase TS by suppressing the growth of ferrite grains after transformation and improving toughness, and (2) transforming the transformation region that becomes pearlite structure into bainite structure or island-like martensite structure. If the speed is less than 2℃/sec, there is no effect of forming bainite structure, etc., while if the rate is less than 2℃/sec,
If the cooling rate exceeds sec, a lumpy martensitic structure will be generated and the toughness will deteriorate significantly, so the cooling rate should be set to 2.
It is necessary to keep it within the range of ~40℃/sec. Furthermore, if the cooling stop temperature is 500°C or higher, the amount of bainite and martensitic structures generated is insufficient, and the TS rises to less than 5 kgf/mm 2 compared to air-cooled materials. The stop temperature must be less than 500℃. The reason for performing light reduction at a reduction rate of 0.5% to less than 20% in the temperature range from less than 500℃ to 200℃ or more after cooling is stopped is mainly to increase YS, YS under light pressure
On the other hand, if light pressure is applied in a temperature range lower than 200℃, hydrogen defects will occur because hydrogen cannot be removed sufficiently, so the temperature range for applying light pressure is 500℃.
It must be within the range of below 200℃.
The rolling reduction rate of light rolling is as shown in Figure 2.
If it is less than 0.5%, there is no noticeable effect on increasing YS, while if it is more than 20%, separation will occur on the shear peace impact fracture surface, so the reduction rate in the temperature range from less than 500℃ to more than 200℃ is 0.5% to 20%. Must be within the range below. The reason why air cooling or slow cooling is performed in a temperature range below 200°C is to facilitate the removal of hydrogen and prevent hydrogen defects. Next, the present invention will be explained with reference to examples. Examples The mechanical properties of steel plates obtained by processing the test steel types whose compositions are shown in Table 1 under the rolling-cooling conditions shown in Table 2 are shown in the same table.
【表】【table】
【表】【table】
【表】
第2表に示す実験例1〜10は本発明の成分組成
を有するA1の鋼片について種々の圧延―冷却条
件により製造したものであり、第2表によれば、
実験例1は圧延後加速冷却を施しておらず、実験
例5は加速冷却を施しているが500℃以上で冷却
を停止したため、いずれもTSが50Kgf/mm2未満
であることがわかり、実験例2は冷却後の軽圧下
がないためLYSが36Kgf/mm2であることがわか
り、実験例3はAr3+70℃からAr3までの圧下率
が50%未満であるためvTrsが−40℃であること
がわかり、実験例9は冷却停止温度が200℃以下
となつているため含有H2による割れが発生して
いることがわかり、実験例10は(α+γ)2相域
で圧延を施しているためセパレーシヨンが発生し
ていることがわかり、実験例4,6,7,8は本
発明の全ての構成要件の範囲内において製造をな
したため適用鋼種の拡大の目標の1つである造船
用YP36キロ鋼の規格に示されているLYS36Kg
f/mm2以上TS50Kgf/mm2以上、vTrs−40℃以下
の条件をいずれも十分に満足していることがわか
る。
実験例11は本発明の圧延―冷却条件の範囲内に
おいて製造されているが、成分組成が第1表に示
すB1鋼をもちいたため、Tiが含有されていない
のでvTrsが−40℃以上であることがわかる。
実験例12,13は従来の製造方法であるNorma材
QTの50キロ級の比較鋼の機械的性質を示してお
り、本発明鋼のCeqは比較鋼のCeqに比べNorma
材においては0.08%も少なくQT材においては
0.03%も少ないことがわかる。
実験例14〜22は、本発明の構成要件の範囲内に
おいて製造をなしており、特に成分組成において
はNi,Cu,Cr,Ca等を適性に含有しており、実
験例14によればTS50キロ級、実験例15〜20によ
ればTS60キロ級、実験例21〜22によればTS70キ
ロ級の高張力鋼を得ることができることがわか
る。
以上実施例からもわかるように本発明の製造方
法によれば低炭素当量で高降伏強度を有し、シヤ
ルピー衝撃破面のセパレーシヨン現象がなく、
vTrsの低い溶接性と低温靭性の優れた高張力鋼
板を安価にかつ安定して製造することができる。[Table] Experimental Examples 1 to 10 shown in Table 2 were produced using A1 steel slabs having the composition of the present invention under various rolling-cooling conditions. According to Table 2,
In Experimental Example 1, accelerated cooling was not performed after rolling, and in Experimental Example 5, accelerated cooling was performed, but cooling was stopped at 500°C or higher, so it was found that the TS was less than 50 Kgf/mm 2 in both cases, and the experiment In Example 2, LYS was found to be 36Kgf/mm 2 because there was no light reduction after cooling, and in Experimental Example 3, vTrs was -40℃ because the reduction rate from Ar 3 +70℃ to Ar 3 was less than 50%. It was found that in Experimental Example 9, the cooling stop temperature was below 200°C, so cracking occurred due to the contained H2 , and in Experimental Example 10, rolling was performed in the (α + γ) two-phase region. It was found that separation occurred due to the presence of steel, and Experimental Examples 4, 6, 7, and 8 were manufactured within the scope of all the constituent requirements of the present invention, so this is one of the goals for expanding the applicable steel types. LYS36Kg shown in the standard of YP36kg steel for shipbuilding
It can be seen that the conditions of f/ mm2 or more, TS50Kgf/ mm2 or more, and vTrs-40°C or less are all fully satisfied. Experimental Example 11 was manufactured within the range of rolling-cooling conditions of the present invention, but since it used B1 steel whose composition is shown in Table 1, it did not contain Ti, so vTrs was -40°C or higher. I understand that. Experimental examples 12 and 13 are Norma material, which is the conventional manufacturing method.
It shows the mechanical properties of QT's 50 kg class comparative steel, and the Ceq of the invention steel is Normal compared to the Ceq of the comparative steel.
In the case of QT material, it is less than 0.08%.
It can be seen that it is less than 0.03%. Experimental Examples 14 to 22 were manufactured within the scope of the constituent requirements of the present invention, and in particular, the component composition appropriately contained Ni, Cu, Cr, Ca, etc. According to Experimental Example 14, TS50 It can be seen that it is possible to obtain high tensile strength steel of kg class, TS60 kg class according to Experimental Examples 15 to 20, and TS70 kg class according to Experimental Examples 21 to 22. As can be seen from the above examples, the manufacturing method of the present invention has a low carbon equivalent and high yield strength, and there is no separation phenomenon on the shear peace impact fracture surface.
High-strength steel plates with low vTrs weldability and excellent low-temperature toughness can be produced inexpensively and stably.
第1図は制御圧延後の加速冷却条件(冷却速
度、冷却停止温度)が引張り特性とシヤルピー衝
撃特性に及ぼす影響を示す図、第2図は加速冷却
後に400℃における軽圧下量が引張り特性とシヤ
ルピー衝撃特性に及ぼす影響(制御圧延後10℃/
secの冷却速度で450℃まで冷却)を示す図であ
る。
Figure 1 shows the influence of accelerated cooling conditions (cooling rate, cooling stop temperature) on tensile properties and sharpie impact properties after controlled rolling, and Figure 2 shows the effects of light reduction at 400°C on tensile properties after accelerated cooling. Effect on Shapey impact properties (10℃/after controlled rolling)
FIG.
Claims (1)
%,Ti0.003〜0.04%,Al0.005〜0.08%,S0.008
%以下,N0.0010%を越え0.010%未満でかつTi含
有量との関係においてN含有量を下式の範囲内と
なして含有し、 Ti%/3.4−0.0020%<N<Ti%/3.4+0.00
20% 残部Feおよび不可避的不純物よりなる鋼片をAr3
+70℃からAr3までの温度域で50〜90%の圧下率
で圧延を施し、その後直ちに2〜40℃/secの加
速冷却速度で500℃未満の温度になるまで冷却を
施し、次いで加速冷却を停止した後500℃未満か
ら200℃以上の温度域で圧下率が0.5以上から20%
未満の範囲内の圧下を施し、その後空冷ないし徐
冷することを特徴とする溶接性と低温靭性の優れ
た高張力鋼の製造方法。 2 C0.005〜0.15%,Si0.1〜0.5%,Mn0.8〜2.0
%,Ti0.003〜0.04%,Al0.005〜0.08%,S0.008
%以下,N0.0010%を越え0.010%未満でかつTi含
有量との関係においてN含有量を下式の範囲内と
なし Ti%/3.4−0.0020%<N<Ti%/3.4+0.00
20% さらに下記(a)群、(b)群の中から選ばれるいずれか
1群または2群を含有し、残部Feおよび不可避
的不純物よりなる鋼片をAr3+70℃からAr3まで
の温度域で50〜90%の圧下率で圧延を施し、その
後直ちに2〜40℃/secの加速冷却速度で500℃未
満の温度になるまで冷却を施し、次いで加速冷却
を停止した後500℃未満から200℃以上の温度域で
圧下率が0.5%以上から20%未満の範囲内の圧下
を施し、その後空冷ないし徐冷することを特徴と
する溶接性と低温靭性の優れた高張力鋼の製造方
法。 (a)群:V0.01〜0.10%,Cu0.5%以下, Ni0.5%以下,Cr0.5%以下, Mo0.5%以下のなかから選ばれる何れか1種
または2種以上。 (b)群:Ca0.002〜0.010%,REM0.005〜0.010%の
なかから選ばれる何れか1種または2種。[Claims] 1 C0.005-0.15%, Si0.1-0.5%, Mn0.8-2.0
%, Ti0.003~0.04%, Al0.005~0.08%, S0.008
% or less, more than 0.0010% and less than 0.010%, and in relation to the Ti content, the N content is within the range of the following formula, Ti%/3.4-0.0020%<N<Ti% /3.4+0.00
A steel billet consisting of 20% balance Fe and unavoidable impurities is heated to Ar 3
Rolling is performed at a reduction rate of 50 to 90% in the temperature range from +70°C to Ar 3 , followed by immediate cooling at an accelerated cooling rate of 2 to 40°C/sec until the temperature is below 500°C, and then accelerated cooling. After stopping, the reduction rate is 0.5 or more to 20% in the temperature range from less than 500℃ to 200℃ or more.
1. A method for producing high-strength steel with excellent weldability and low-temperature toughness, characterized by applying a reduction within a range of less than or equal to 100 ml, followed by air cooling or gradual cooling. 2 C0.005~0.15%, Si0.1~0.5%, Mn0.8~2.0
%, Ti0.003~0.04%, Al0.005~0.08%, S0.008
% or less, more than 0.0010% and less than 0.010%, and in relation to the Ti content, the N content must be within the range of the following formula: Ti%/3.4-0.0020%<N<Ti%/3.4+0 .00
20% A steel billet containing one or two groups selected from the following groups (a) and (b), with the balance consisting of Fe and unavoidable impurities, is heated at a temperature from Ar 3 +70℃ to Ar 3 Rolling is performed at a rolling reduction rate of 50 to 90% in the area, and then immediately cooled at an accelerated cooling rate of 2 to 40°C/sec until the temperature is below 500°C, and then after stopping the accelerated cooling, the rolling process is performed from below 500°C. A method for manufacturing high-strength steel with excellent weldability and low-temperature toughness, characterized by applying rolling reduction in the range of 0.5% or more to less than 20% in a temperature range of 200°C or higher, followed by air cooling or slow cooling. . Group (a): One or more selected from V0.01-0.10%, Cu0.5% or less, Ni0.5% or less, Cr0.5% or less, Mo0.5% or less. Group (b): Any one or two selected from Ca0.002-0.010% and REM0.005-0.010%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21916682A JPS59110725A (en) | 1982-12-16 | 1982-12-16 | Preparation of high tensile steel excellent in weldability and low temperature toughness |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP21916682A JPS59110725A (en) | 1982-12-16 | 1982-12-16 | Preparation of high tensile steel excellent in weldability and low temperature toughness |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS59110725A JPS59110725A (en) | 1984-06-26 |
| JPS625215B2 true JPS625215B2 (en) | 1987-02-03 |
Family
ID=16731231
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP21916682A Granted JPS59110725A (en) | 1982-12-16 | 1982-12-16 | Preparation of high tensile steel excellent in weldability and low temperature toughness |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS59110725A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2668169B1 (en) * | 1990-10-18 | 1993-01-22 | Lorraine Laminage | IMPROVED WELDING STEEL. |
-
1982
- 1982-12-16 JP JP21916682A patent/JPS59110725A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS59110725A (en) | 1984-06-26 |
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