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JPS622613B2 - - Google Patents
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JPS622613B2 - - Google Patents

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Publication number
JPS622613B2
JPS622613B2 JP22034082A JP22034082A JPS622613B2 JP S622613 B2 JPS622613 B2 JP S622613B2 JP 22034082 A JP22034082 A JP 22034082A JP 22034082 A JP22034082 A JP 22034082A JP S622613 B2 JPS622613 B2 JP S622613B2
Authority
JP
Japan
Prior art keywords
less
rolling
toughness
cooling
temperature
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
JP22034082A
Other languages
Japanese (ja)
Other versions
JPS59113120A (en
Inventor
Chiaki Shiga
Taneo Hatomura
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.)
JFE Steel Corp
Original Assignee
Kawasaki 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 Kawasaki Steel Corp filed Critical Kawasaki Steel Corp
Priority to JP22034082A priority Critical patent/JPS59113120A/en
Publication of JPS59113120A publication Critical patent/JPS59113120A/en
Publication of JPS622613B2 publication Critical patent/JPS622613B2/ja
Granted legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D8/00Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment

Landscapes

  • 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

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

本発明は、溶接性と低温靭性の優れた低炭素当
量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
等を調質処理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厚
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
冷却による方法によれば、第1図に示すC0.06
%、Mn1.4%、Ceq0.29%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ができるが、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低炭素
当量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つて
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℃未満から200℃以上の温
度域で圧下率0.5%から20%未満の軽圧下を施す
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
て日夜研鑚の結果、本発明の特許請求の範囲記載
の成分組成に示すNbを含有させ、更にNbを固溶
状態となしてCRを施し、その後直ちに加速冷却
をなすことによりフエライトやベイナイト等の組
織が一段と微細化されるので、加速冷却停止後軽
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。 すなわちNb含有鋼にCRを施しその後直ちに加
速冷却を施すことにより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材の炭素当量
(以下Ceqと称す)以下で高張力を得ることがで
き前記に示す適用鋼種の拡大を容易になすことが
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
化するので、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。 Nbはフエライトの細粒化に効果があるが0.005
%未満ではその効果がなく、一方0.1%を越える
と溶接時に溶接金属に拡散し、溶接金属の靭性を
低下させるので、Nbは0.005〜0.1%の範囲内にす
る必要がある。 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、REM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%
を越えて添加する必要はなく、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
に添加されるが、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
保のために添加されるが、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。 Nbが少なくとも0.005%固溶する温度まで加熱
した後、Ar3+150℃からAr3までの温度域で50〜
90%の圧下率で圧延を施す理由は、固溶Nbの未
再結晶γ域の開始温度は未固溶Nbの上記開始温
度がAr3+70℃であるのに比べAr3+150℃と高
く、未再結晶γ域を拡大することができ、また未
再結晶γ域での圧下により、変形帯を有効に生成
することができ、これらはいずれもフエライトの
細粒化を促進させ靭性を高める効果があるが、固
溶Nbは0.005%未満では十分その効果を得ること
ができないので、Nbが少なくとも0.005%固溶す
る温度に加熱する必要がある。 圧延仕上げ温度域をAr3+150℃からAr3まで限
定する理由は、上記固溶Nbの未再結晶γ域の開
始温度であるAr3+150℃から圧延を施すことに
よりフエライト核となる変形帯が生成され、一方
Ar3より低い温度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+150℃〜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℃
未満の温度まで加速冷却を施すのは(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
靭性が劣化させるので、冷却速度は2〜40℃/sec
の範囲内にする必要がある。また加速冷却停止温
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、強度が不足しQT鋼の代替
とならないので、加速冷却停止温度は500℃未満
にする必要がある。 加速冷却停止後500℃未満から200℃以上の温度
域において0.5%以上から20%未満の圧下率で軽
圧下を施す理由は、主としてYSを上昇させるこ
とにあり、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、圧下
率は0.5%以上から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
施すのは、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 producing low-carbon equivalent high-strength steel with excellent weldability and low-temperature toughness, and in particular, the present invention relates to a method for manufacturing a low-carbon equivalent high-strength steel with excellent weldability and low-temperature toughness. The present invention relates to a method for manufacturing high-strength steel plates for shipbuilding, steel plates for pressure vessels such as tanks for butane and propane, steel plates for line pipes for cold regions, etc., without thermal treatment. Conventionally, high-strength steel plates 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. In addition, controlled rolling (hereinafter referred to as CR) is a manufacturing method that does not apply heat treatment, so-called non-thermal treatment, to achieve high tensile strength and high toughness.
However, in order to achieve high tensile strength with CR material that can replace Norma and QT materials, it is necessary to lower the finish rolling temperature of CR, which not only significantly reduces rolling efficiency but also reduces the Separation occurs on the shear peace impact fracture surface, which is disliked by users and makes it difficult to expand the range of applicable steel types. CR that improves the above drawbacks of CR up to low temperature range
As a manufacturing method that achieves high tensile strength without requiring rolling, there is a method of accelerated cooling after rolling.According to this accelerated cooling method, the C0.06
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 steel plates containing %, Mn1.4%, and Ceq0.29%, increasing the cooling rate TS can be easily increased by , but on the other hand, 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, steel produced by accelerated cooling is limited in steel types that can be substituted for Norma and QT materials, and is still not fully satisfied. The present invention provides a low-carbon equivalent high-strength steel with excellent weldability and low-temperature toughness, which eliminates the drawbacks seen in the conventional manufacturing methods described above, and provides improved productivity and an inexpensive manufacturing method without heat treatment. The object can be achieved by providing the method described in the claims. Next, the present invention will be explained in detail. As a result of studying a method to increase YS without heat treatment, the inventors of the present invention found that accelerated cooling is performed immediately after rolling, and the rolling reduction rate is from 0.5% to less than 20% in the temperature range from less than 500°C to more than 200°C. We have newly found that YS increases significantly by applying light pressure reduction. 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
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. However, a problem arose in that it was difficult to apply to steel types that required low-temperature toughness. As a result of day and night research into a method for improving low-temperature toughness, the present inventors have incorporated Nb as shown in the component composition described in the claims of the present invention, and further applied CR with Nb in a solid solution state, Immediately after that, accelerated cooling further refines the structure of ferrite, bainite, etc., so even if light reduction is applied after stopping accelerated cooling, there is less deterioration in toughness, and YS,
The present invention was conceived after further discovering that TS increases. In other words, by applying CR to Nb-containing steel and then immediately applying 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 at less than the carbon equivalent (hereinafter referred to as Ceq) of Norma and QT materials, making it easy to expand the applicable steel types listed above. can be done. 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 crack resistance will increase. C should be within the range of 0.005 to 0.15% since the deterioration of properties becomes significant. 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. Si must be within the range of 0.1 to 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. Nb is effective in refining ferrite, but 0.005
If it is less than 0.1%, it has no effect, while if it exceeds 0.1%, it will diffuse into the weld metal during welding and reduce the toughness of the weld metal, so Nb needs to be in the range of 0.005 to 0.1%. The above are the basic components of the steel slab used in the present invention, and if necessary, Ni, Mo, Cu,
At least one selected from V, Cr, Ca, and REM can be added, and proper inclusion of each element adds a unique effect as described below. 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 Mo in excess of 0.5%, and any more will increase manufacturing costs, so Mo should be added at 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 must be kept at 0.5% or less. V is added to improve the strength and toughness of the base metal of steel plates and ensure joint strength, but if it is less than 0.01%, it has no effect, while if it exceeds 0.10%, it will significantly deteriorate the toughness of the base metal and HAZ. V is 0.01~0.10%
Must be within the range. 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 R EM 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 R EM 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 to a temperature at which at least 0.005% Nb is dissolved in solid solution, heating in the temperature range from Ar 3 + 150℃ to Ar 3
The reason why rolling is performed at a rolling reduction ratio of 90% is that the onset temperature of the non-recrystallized γ region of solid-dissolved Nb is higher at Ar 3 +150°C, compared to the above-mentioned starting temperature of Ar 3 +70°C for undissolved Nb. The unrecrystallized γ region can be expanded, and deformation bands can be effectively generated by rolling down the unrecrystallized γ region, both of which have the effect of promoting grain refinement of ferrite and increasing toughness. However, if the solid solution Nb is less than 0.005%, the effect cannot be obtained sufficiently, so it is necessary to heat to a temperature at which at least 0.005% Nb is dissolved. The reason why the rolling finishing temperature range is limited from Ar 3 +150°C to Ar 3 is that by rolling from Ar 3 +150°C, which is the starting temperature of the non-recrystallized γ region of solid solute Nb, a deformation zone that becomes a ferrite nucleus is formed. generated, while
If rolling is performed at a temperature lower than Ar 3 , separation will occur on the Shapey impact fracture surface, so the rolling temperature range needs to be within the range of Ar 3 +150°C to Ar 3 .
Furthermore, during rolling in the above temperature range, the rolling reduction rate was increased to 50
The reason for limiting the rolling reduction to ~90% is that if the rolling reduction is less than 50%, the formation of deformation bands within the austenite grains is insufficient, so by applying accelerated cooling after rolling, which will be described later, the ferrite grains will not become finer. Since massive bainite is generated, toughness is significantly deteriorated. On the other hand, 90
If rolling is performed at a reduction rate exceeding 50%, the introduced deformation band will be saturated, and even if subsequent accelerated cooling is performed, the effect of improving toughness will be small. Must be within the range of %. Immediately after rolling, heat to 500℃ at a cooling rate of 2 to 40℃/sec.
The purpose of accelerated cooling to a temperature below The main purpose is to increase TS by transforming into TS, but if the cooling rate is less than 2°C/sec, there is no effect of generating bainite structure, etc., while if it exceeds 40°C/sec, a lumpy martensite structure is generated. The cooling rate should be 2 to 40℃/sec as it will significantly deteriorate the toughness.
Must be within the range. In addition, when the accelerated cooling stop temperature is 500℃ or higher, the amount of bainite and martensitic structure generated is insufficient, and the TS rise is less than 5Kgf/mm 2 compared to air-cooled materials, and the strength is insufficient and it cannot be used as a substitute for QT steel. The stop temperature must be less than 500℃. The reason for performing light reduction at a reduction rate of 0.5% or more to less than 20% in the temperature range from less than 500°C to more than 200°C after stopping accelerated cooling is mainly to increase YS, and to under pressure
If the increase in YS is small and 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 in which light pressure is applied is 500℃.
It must be within the range of below ℃ to 200℃ or higher. If the reduction rate of light reduction is less than 0.5%, it will not have a significant 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 should be within the range of 0.5% or more and less than 20%. It is necessary to 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 sheets prepared 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No.1〜11は本発明の成分組
成を有するA1の鋼片について種々の加熱―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No.1〜4はNbの固溶条件、圧延条
件、冷却条件、冷却後の軽圧下条件、徐冷開始条
件特の本発明の全ての構成要件の範囲内において
製造されているため、適用鋼種の拡大の目標の1
つとする溶接用構造用高張力鋼板の規格に示す
WES―135、HW36の機械的性質の基準である
LYS36Kgf/mm2以上、TS53Kgf/mm2以上の値を非常
に低い炭素当量で得ることができ、さらに低温靭
性も優れていることがわかる。 実験例No.5〜14は本発明の構成要件のいずれか
が満足されていないため溶接用構造用高張力鋼の
規格(たとえばHW36)を満足することができな
いことがわかる。すなわち実験例No.5は圧延後加
速冷却を施さず空冷(以下ACと称す)したもの
であるため、また実験例No.11は固溶Nb量が0.005
%未満であるためいずれも目標とするTS53Kgf/
mm2を満足していないことがわかり、実験例No.6は
冷却後の軽圧下を施しておらないためLYSが36Kg
f/mm2を満足していないことがわかり、実験例No.7
はAr3+150℃からAr3までの圧下率が50%未満で
あるため、vTrsが目標とする−40℃より高いこ
とがわかり、実験例No.9は軽圧下後の徐冷開始温
度が200℃未満であるため、水素割れが起つてい
ることがわかり、実験例No.10はAr3以下の温度で
圧下率30%の圧延を施したためセパレーシヨンが
発生していることがわかる。 実験例No.15〜23は本発明の構成要件の範囲内に
おいて製造されており、特に成分組成において
Ni、Cu、Cr、Mo、V、Ca、REM等を適正に含
有しておるので、実験例15〜19によれば60Kgf/mm2
級、実験例20、21によれば70Kgf/mm2級、そして実
験例22、23によれば80Kgf/mm2級の鋼板を、非常に
低い炭素当量でLYSとTSのバランスもよく、さ
らに低温靭性の優れたかつシヤルピー衝撃破面に
セパレーシヨンの発生もなしに、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、低炭素当量で溶接性が優れた、シヤ
ルピー衝撃破面にセパレーシヨンの発生しない、
vTrsの低い、低温靭性の優れた低炭素当量高張
力鋼を安価にかつ安定して製造することができ
る。
[Table] Experimental examples Nos. 1 to 11 shown in Table 2 are those produced using A1 steel slabs having the composition of the present invention under various heating-rolling-cooling conditions. Examples Nos. 1 to 4 are manufactured within the scope of all the constituent requirements of the present invention, including Nb solid solution conditions, rolling conditions, cooling conditions, light reduction conditions after cooling, and slow cooling start conditions, so they are applicable. Goal 1 of expanding steel types
As shown in the standards for high-strength steel plates for structural use for welding.
WES-135 is the standard for mechanical properties of HW36
It can be seen that values of LYS36Kgf/mm 2 or higher and TS53Kgf/mm2 or higher can be obtained with a very low carbon equivalent, and the low-temperature toughness is also excellent. It can be seen that Experimental Examples Nos. 5 to 14 cannot satisfy the standards for high-strength structural steel for welding (for example, HW36) because any of the constituent requirements of the present invention are not satisfied. In other words, Experimental Example No. 5 was air-cooled (hereinafter referred to as AC) without accelerated cooling after rolling, and Experimental Example No. 11 had a solid solution Nb amount of 0.005.
Since it is less than %, both targets are TS53Kgf/
mm 2 was not satisfied, and in Experimental Example No. 6, the LYS was 36 kg because light compression was not applied after cooling.
It was found that f/mm 2 was not satisfied, and Experimental Example No. 7
Since the rolling reduction rate from Ar 3 +150℃ to Ar 3 is less than 50%, it can be seen that vTrs is higher than the target -40℃, and in Experimental Example No. 9, the slow cooling start temperature after light pressure reduction is 200℃. It can be seen that hydrogen cracking occurs because the temperature is less than 0.degree. C., and in Experimental Example No. 10, separation occurs because rolling was performed at a temperature of Ar 3 or less with a reduction ratio of 30%. Experimental examples Nos. 15 to 23 were manufactured within the scope of the constituent requirements of the present invention, especially in terms of component composition.
It contains Ni, Cu, Cr, Mo, V, Ca, REM, etc. appropriately, so according to Experimental Examples 15 to 19, it is 60Kgf/mm 2
According to Experimental Examples 20 and 21, the steel plate is 70Kgf/mm 2nd grade, and according to Experimental Examples 22 and 23, 80Kgf/mm 2nd grade steel plate has a very low carbon equivalent, a good balance of LYS and TS, and a low temperature. It can be seen that excellent toughness can be obtained with no separation occurring on the Charpey impact fracture surface. As can be seen from the above examples, the manufacturing method of the present invention has a low carbon equivalent, excellent weldability, and no separation on the shear py impact fracture surface.
Low carbon equivalent high tensile strength steel with low vTrs and excellent low temperature toughness can be produced inexpensively and stably.

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

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
におよぼす影響を示す図である。
The figure shows the influence of accelerated cooling conditions (cooling rate, cooling stop temperature) after controlled rolling on tensile properties and Charpy impact properties.

Claims (1)

【特許請求の範囲】 1 C0.005〜0.15%、Si0.1〜0.5%、Mn0.8〜2.0
%、Nb0.005〜0.1%、Al 0.005〜0.08%、S0.008
%以下を含有し、残部Feおよび不可避的不純物
よりなる鋼片を、鋼片に含有されているNbが少
なくとも0.005%固溶する温度に加熱した後、Ar3
+150℃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の冷
却速度で500℃未満の温度まで冷却をなし、冷却
停止後500℃未満から200℃以上の温度域で0.5%
以上から20%未満の圧下率で圧延を施し、引続き
空冷ないし徐冷することを特徴とする溶接性と保
温靭性の優れた低炭素当量高張力鋼の製造方法。 2 C0.005〜0.15%、Si0.1〜0.5%、Mn0.8〜2.0
%、Nb0.005〜0.1%、Al 0.005〜0.08%、S0.008
%以下を含有し、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、鋼片
に含有されているNbが少なくとも0.005%固溶す
る温度に加熱した後、Ar3+150℃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の冷却速度で500℃未満の温
度まで冷却をなし、冷却停止後500℃未満から200
℃以上の温度域で0.5%以上から20%未満の圧下
率で圧延を施し、引続き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低炭素当
量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
%, Nb0.005~0.1%, Al 0.005~0.08%, S0.008
% or less, with the remainder consisting of Fe and unavoidable impurities .
Rolling is performed at a reduction rate of 50 to 90% in the temperature range from +150℃ to Ar 3 , and then immediately cooled to a temperature of less than 500℃ at a cooling rate of 2 to 40℃/sec, and after cooling is stopped, it is less than 500℃. 0.5% in the temperature range from to 200℃ or higher
From the above, a method for producing low carbon equivalent high tensile strength steel with excellent weldability and heat retention toughness, which is characterized by rolling at a reduction rate of less than 20% and subsequent air cooling or slow cooling. 2 C0.005~0.15%, Si0.1~0.5%, Mn0.8~2.0
%, Nb0.005~0.1%, Al 0.005~0.08%, S0.008
% or less, and further contains one or two groups selected from the following groups (a) and (b), and the remainder
After heating a steel slab consisting of Fe and unavoidable impurities to a temperature at which at least 0.005% of Nb contained in the steel slab becomes a solid solution, it is reduced by 50 to 90% in a temperature range from Ar 3 +150℃ to Ar 3 . Rolling is carried out at a cooling rate of 2 to 40℃/sec.
A method for producing a low carbon equivalent high tensile strength steel with excellent weldability and low temperature toughness, which is characterized by rolling at a reduction rate of 0.5% or more to less than 20% in a temperature range of ℃ or higher, followed by air cooling or slow cooling. Group (a): V0.01~0.10%, Cu0.5% or less, Ni0.5%
One or more types selected from the following: Cr 0.5% or less, Mo 0.5% or less. Group (b): Ca0.002-0.010%, REM0.005-0.010%
One or two selected from
seed.
JP22034082A 1982-12-17 1982-12-17 Production of low carbon equivalent high tensile steel having excellent weldability and low temperature toughness Granted JPS59113120A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP22034082A JPS59113120A (en) 1982-12-17 1982-12-17 Production of low carbon equivalent high tensile steel having excellent weldability and low temperature toughness

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP22034082A JPS59113120A (en) 1982-12-17 1982-12-17 Production of low carbon equivalent high tensile steel having excellent weldability and low temperature toughness

Publications (2)

Publication Number Publication Date
JPS59113120A JPS59113120A (en) 1984-06-29
JPS622613B2 true JPS622613B2 (en) 1987-01-21

Family

ID=16749609

Family Applications (1)

Application Number Title Priority Date Filing Date
JP22034082A Granted JPS59113120A (en) 1982-12-17 1982-12-17 Production of low carbon equivalent high tensile steel having excellent weldability and low temperature toughness

Country Status (1)

Country Link
JP (1) JPS59113120A (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62205230A (en) * 1986-03-04 1987-09-09 Kobe Steel Ltd Manufacture of steel plate for low temperature service superior in characteristic for stopping brittle cracking propagation
CN100396809C (en) * 2005-09-12 2008-06-25 鞍钢股份有限公司 Thick steel plate with high input energy and low welding crack sensitivity and production method thereof
CN110714171B (en) * 2019-10-13 2021-08-24 河钢股份有限公司 A kind of high ductility EH420 grade ship plate steel and its production method

Also Published As

Publication number Publication date
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