JPS58733B2 - Method for manufacturing non-temperature high tensile strength hot rolled steel strip for processing - Google Patents
Method for manufacturing non-temperature high tensile strength hot rolled steel strip for processingInfo
- Publication number
- JPS58733B2 JPS58733B2 JP4241178A JP4241178A JPS58733B2 JP S58733 B2 JPS58733 B2 JP S58733B2 JP 4241178 A JP4241178 A JP 4241178A JP 4241178 A JP4241178 A JP 4241178A JP S58733 B2 JPS58733 B2 JP S58733B2
- Authority
- JP
- Japan
- Prior art keywords
- temperature
- less
- tensile strength
- elements
- transformation
- 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
Links
- 229910000831 Steel Inorganic materials 0.000 title claims description 23
- 239000010959 steel Substances 0.000 title claims description 23
- 238000004519 manufacturing process Methods 0.000 title claims description 8
- 238000000034 method Methods 0.000 title description 14
- 238000001816 cooling Methods 0.000 claims description 32
- 238000005096 rolling process Methods 0.000 claims description 30
- 230000009466 transformation Effects 0.000 claims description 29
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 14
- 230000003014 reinforcing effect Effects 0.000 claims description 11
- 229910052802 copper Inorganic materials 0.000 claims description 9
- 239000010949 copper Substances 0.000 claims description 9
- 229910052804 chromium Inorganic materials 0.000 claims description 8
- 238000004804 winding Methods 0.000 claims description 8
- 229910052742 iron Inorganic materials 0.000 claims description 7
- 229910052750 molybdenum Inorganic materials 0.000 claims description 7
- 238000005098 hot rolling Methods 0.000 claims description 6
- 239000000203 mixture Substances 0.000 claims description 6
- 229910000859 α-Fe Inorganic materials 0.000 claims description 6
- 229910052759 nickel Inorganic materials 0.000 claims description 5
- 230000009467 reduction Effects 0.000 claims description 5
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 claims description 4
- 229910052748 manganese Inorganic materials 0.000 claims description 4
- 229910052758 niobium Inorganic materials 0.000 claims description 4
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 229910052720 vanadium Inorganic materials 0.000 claims description 4
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 229910052749 magnesium Inorganic materials 0.000 claims description 3
- 229910052761 rare earth metal Inorganic materials 0.000 claims description 3
- 229910052726 zirconium Inorganic materials 0.000 claims description 3
- 229910052719 titanium Inorganic materials 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims 5
- 229910001563 bainite Inorganic materials 0.000 description 37
- 230000000694 effects Effects 0.000 description 20
- 238000010791 quenching Methods 0.000 description 9
- 230000000171 quenching effect Effects 0.000 description 9
- 238000005728 strengthening Methods 0.000 description 9
- 230000007423 decrease Effects 0.000 description 8
- 238000010586 diagram Methods 0.000 description 7
- 229910000734 martensite Inorganic materials 0.000 description 7
- 229910001562 pearlite Inorganic materials 0.000 description 7
- 239000006104 solid solution Substances 0.000 description 6
- 239000000126 substance Substances 0.000 description 6
- 230000000052 comparative effect Effects 0.000 description 5
- 238000010438 heat treatment Methods 0.000 description 5
- 229910001566 austenite Inorganic materials 0.000 description 4
- 230000006866 deterioration Effects 0.000 description 4
- 229920006395 saturated elastomer Polymers 0.000 description 4
- 238000007792 addition Methods 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 2
- 238000007796 conventional method Methods 0.000 description 2
- 230000007246 mechanism Effects 0.000 description 2
- 230000001105 regulatory effect Effects 0.000 description 2
- 238000005482 strain hardening Methods 0.000 description 2
- 150000003568 thioethers Chemical class 0.000 description 2
- 229910000746 Structural steel Inorganic materials 0.000 description 1
- 229910010055 TiB Inorganic materials 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000004881 precipitation hardening Methods 0.000 description 1
- 238000003672 processing method Methods 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 230000002787 reinforcement Effects 0.000 description 1
- 230000000979 retarding effect Effects 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
Landscapes
- Heat Treatment Of Steel (AREA)
- Heat Treatment Of Sheet Steel (AREA)
- Heat Treatment Of Strip Materials And Filament Materials (AREA)
Description
【発明の詳細な説明】
本発明は、熱延鋼帯の製造方法に係り、特に靭性、冷間
加工性、溶接性等がともにすぐれた高張力鋼板の製造方
法に関する。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a method for producing a hot-rolled steel strip, and particularly to a method for producing a high-strength steel plate with excellent toughness, cold workability, weldability, etc.
冷間加工用の高張力熱延鋼板には、高い強度水準とすぐ
れた加工性が同時に要求されるが、一般に、強度を増大
させると加工性が低下する傾向にあり、それらの調和あ
る向上が希求されている。High-strength hot-rolled steel sheets for cold working require a high level of strength and excellent workability at the same time, but in general, increasing strength tends to reduce workability, so it is important to improve these in a harmonious manner. It is desired.
すなわち、強度を増大させるにともない、伸び、張り出
し性、伸びフランジ性等の加工性因子が低下する上に、
成形時におけるスプリングバック量の増大に起因する形
状凍結性悪化の問題や加工力の増大化にともなう設備、
機械面での不利といった種々の障害が発生する。In other words, as the strength increases, workability factors such as elongation, stretchability, stretch flangeability, etc. decrease, and
Problems with deterioration of shape fixability due to increased springback during molding and equipment due to increased processing force,
Various obstacles arise, such as mechanical disadvantages.
これらの加工性に関する問題は、素材の降伏応力が相対
的に高い場合に著しくなることが知られている。It is known that these problems regarding workability become significant when the yield stress of the material is relatively high.
ちなみに、冷間加工用に適用されている所謂高張力熱延
鋼板は、一般に引張強度は60kg/mm2以上、降伏
点は45kg/mm2以上であるが、この際、引張強度
を高めると降伏点も上昇するばかりか前者に対する後者
の比(降伏比)は一層高くなり、これにつれて成形性が
飛躍的に困難になる場合が多い。By the way, so-called high-strength hot-rolled steel sheets used for cold working generally have a tensile strength of 60 kg/mm2 or more and a yield point of 45 kg/mm2 or more, but in this case, increasing the tensile strength also increases the yield point. Not only does this increase, but the ratio of the latter to the former (yield ratio) also becomes higher, and as a result, formability often becomes dramatically difficult.
従って、現実的で好ましい高張力鋼とは、素材の状態で
は高い引張強度を有するにもかかわらず降伏応力は可及
的に低く、一方、加工された後では降伏限が所定水準ま
で上昇するようなものと云える。Therefore, a realistic and preferable high-strength steel is one that has as low a yield stress as possible despite having high tensile strength in its raw state, while having a yield limit that rises to a predetermined level after processing. It can be said that it is something.
前記を達成するため、従来より種々の試みがなされてい
るが、未だ充分な結果に到っていない上に、溶接性不良
等の他の欠点をともなう場合も多い。In order to achieve the above, various attempts have been made in the past, but they have not yet achieved satisfactory results and are often accompanied by other drawbacks such as poor weldability.
例えば、鋼板の強度上昇を計るため、鉄スラブに強化元
素等を添加する方法がよく知られている。For example, a well-known method is to add reinforcing elements to an iron slab in order to increase the strength of the steel plate.
この方法は、主強化元素としてNb、V、TiB等を用
い、これら元素による析出強化と細粒化作用を主たる強
化機構として活用する一方、補助的に添加するSi、M
n、Ni、C1l、Cr、Mo等の固溶硬(強)化作用
によって強度上昇を達成するものであるが、この方法に
よるときは、引張強度に比して降伏応力の増加割合が大
きいため、降伏比が実用上の目安とされる70%を越え
80〜95%に達する欠点がある。This method uses Nb, V, TiB, etc. as the main strengthening elements, and utilizes the precipitation strengthening and grain refining effects of these elements as the main strengthening mechanism, while supplementary additions of Si, M
The strength is increased by the solid solution hardening (strengthening) effect of n, Ni, Cl, Cr, Mo, etc., but when this method is used, the rate of increase in yield stress is large compared to the tensile strength. However, there is a drawback that the yield ratio exceeds 70%, which is considered as a practical guideline, and reaches 80 to 95%.
この欠点を改善するためには、周知の通り、C含有量あ
るいは固溶強化元素の添加量を増加させることが有効で
あるが、前者の場合には、加工性靭性、溶接性に極めて
悪影響があり、後者の場合には、強度上昇のために比較
的多量の添加を必要とし、結果的にC当量の上昇とこれ
にともなう靭性、溶接性の悪化を招くので、これらの手
段による降伏比の低下には限度がある。In order to improve this drawback, as is well known, it is effective to increase the C content or the amount of solid solution strengthening elements added, but in the case of the former, it has a very negative effect on workability toughness and weldability. In the latter case, a relatively large amount of addition is required to increase the strength, resulting in an increase in C equivalent and a concomitant deterioration in toughness and weldability. There is a limit to the decline.
次に、従来他側として、ベイナイト組織を利用する方法
も知られている。Next, as the other side, a method using a bainite structure is also known.
、この方法は、ベイナイト組織の性質、すなわち、比較
的低C当量の化学成分で高強度が得られることおよび変
態時に導入された多数の自由転位のために引張試験時に
土降伏点が現われず、然してフェライト・パーライト・
組織鋼に比して低降伏化が得られることを利用して高強
度、低降伏点の鋼板を得る方法である。, this method is based on the properties of the bainitic structure, i.e., high strength can be obtained with relatively low C equivalent chemical components and a large number of free dislocations introduced during transformation, so that no soil yield point appears during the tensile test. However, ferrite, pearlite,
This is a method to obtain a steel plate with high strength and low yield point by utilizing the fact that it has a lower yield than structural steel.
しかしながら、通常のベイナイト組織とするのみでは、
周知のごとく強度上昇に対する伸びの低下割合が極めて
大きい−すなわち降伏点が低すぎる−ため、加工法が悪
化する。However, if only a normal bainite structure is used,
As is well known, the rate of decrease in elongation relative to the increase in strength is extremely large - that is, the yield point is too low - and this deteriorates the processing method.
本発明の目的は、前記従来技術の欠点をなくし、強化元
素等の低含有量下において、靭性、冷間加工性および溶
接性等がともにすぐれた高張力熱延鋼帯の製造方法を提
供するにある。An object of the present invention is to eliminate the drawbacks of the prior art and provide a method for producing a high-strength hot-rolled steel strip that has excellent toughness, cold workability, weldability, etc. in a low content of reinforcing elements. It is in.
前記目的を達成するため、本発明は、強化元素等を含有
する鉄スラブを熱間圧延するに際1〜、該強化元素等の
含有量をC:0.02〜0.12%(重量、以下同じ)
、Mn:1.0−2.0%、Si:1.0%以下、Mo
:0.05〜1.0%、Al:0.10%以下、S:0
.020%以下にそれぞれ保ち、かつ前記熱間圧延に当
り、前記スラブの加熱を1000〜1300℃で、仕上
圧延を9500以下の開始温度であるが後記TFS以上
の終了温度にてかつ合計川下率50%以上で、冷却を前
記TFS〜後記TBSの温度範囲内にて後記VC以上の
冷却速度でおよび巻取を鋼のMS点〜(TBS−30℃
)の温度範囲内で順次行なうことを特徴とする。In order to achieve the above object, the present invention provides that when hot rolling an iron slab containing reinforcing elements etc., the content of the reinforcing elements etc. is C: 0.02-0.12% (weight, same as below)
, Mn: 1.0-2.0%, Si: 1.0% or less, Mo
: 0.05 to 1.0%, Al: 0.10% or less, S: 0
.. 020% or less, and during the hot rolling, the slab was heated at 1000 to 1300°C, and the finish rolling was performed at a starting temperature of 9500°C or less, but at a finishing temperature of TFS or higher as described later, and a total downstream rate of 50. % or more, cooling is performed within the temperature range of TFS to TBS described below at a cooling rate of VC or higher, and winding is performed to the MS point of the steel ~ (TBS - 30°C
) is characterized in that it is carried out sequentially within the temperature range.
ただし、TFsは準平衡状態における初析フェライト変
態開始温度(℃)、TBSは極微細ベイナイト変態の開
始温度(℃)、VCは極微細ベイナイト組成率を60%
以上とするために必要な冷却速度の下限(℃/S)でそ
れぞれ後代により与えられる。However, TFs is the starting temperature of pro-eutectoid ferrite transformation in a quasi-equilibrium state (℃), TBS is the starting temperature of ultrafine bainite transformation (℃), and VC is the ultrafine bainite composition ratio of 60%.
The lower limit (° C./S) of the cooling rate required to achieve the above is given by each posterity.
本発明において、鉄スラブに含有せしめる強化元素等は
、一般に固溶硬化元素として知られるMn、Si、Mo
の他、強化元素としてのC1脱酸元素としてのAI、不
可避元素としてのS、必要により加えることのある強化
元素例のNb、V。In the present invention, the reinforcing elements contained in the iron slab include Mn, Si, and Mo, which are generally known as solid solution hardening elements.
In addition, C1 is a reinforcing element, AI is a deoxidizing element, S is an unavoidable element, and Nb and V are examples of reinforcing elements that may be added as necessary.
Ti、固溶硬化元素例のCr、Ni、Cu、鋼中硫化物
の形状制御剤例のZr、Mg、Ca、希土類元素および
B等を広く意味する。It broadly refers to Ti, examples of solid solution hardening elements such as Cr, Ni, and Cu, Zr, Mg, Ca, rare earth elements, and B as examples of shape control agents for sulfides in steel.
強化元素等の作用および本発明含有量とする理由は以下
の通りである。The effects of the reinforcing elements and the reason for the content according to the present invention are as follows.
C:強化作用上0.02%以上が必要であるが、0.1
2%を越えると加工性、靭性、溶接性に悪影響を与える
ばかりか後記極微細ベイトナイト組織を形成する上で好
ましくない。C: 0.02% or more is required for strengthening effect, but 0.1%
If it exceeds 2%, it not only adversely affects workability, toughness, and weldability, but also is unfavorable for forming the ultrafine batonite structure described below.
Mn:強化作用およびAr3変態点の低下、フェライト
・パーライト変態の遅延、ベイナイト変態温度の低下等
によって極微細ベイナイト組織を得やすくする作用を有
しており、かかる目的のため1.0%以上が好ましい。Mn: Has the effect of making it easier to obtain an extremely fine bainite structure by strengthening, lowering the Ar3 transformation point, delaying the ferrite-pearlite transformation, lowering the bainite transformation temperature, etc., and for this purpose, 1.0% or more is added. preferable.
しかしながら、2.0%を越えると加工性、靭性、溶接
性を悪化させる上に、圧延集合組織が発達して機械的性
質の異方性を大きくするので好ましくない。However, if it exceeds 2.0%, it is not preferable because it deteriorates workability, toughness, and weldability, and also develops rolling texture and increases the anisotropy of mechanical properties.
Si:固溶硬化元素として降伏比を左程高めることなく
強度上昇作用を有するが、一方でAr3変態点およびベ
イナイト変態温度を上昇させる作用があり、然して1.
0%を越えると極微細ベイナイト組織を得る上で好まし
くないばかりか表面性状の劣化による商品価値の低下原
因にもなる。Si: As a solid solution hardening element, it has the effect of increasing the strength without significantly increasing the yield ratio, but on the other hand, it has the effect of increasing the Ar3 transformation temperature and the bainite transformation temperature, and therefore 1.
If it exceeds 0%, it is not only unfavorable for obtaining an extremely fine bainite structure, but also causes a decrease in commercial value due to deterioration of surface properties.
Mo:極微細ベイナイト組織を得る上で最も重要な元素
である。Mo: The most important element in obtaining an ultrafine bainite structure.
すなわち、フェライトおよびパーライト変態を著しく遅
らせる作用を有しているため極微細ベイナイト組織率の
向上を計り得ることおよび後記する仕上圧延中からの冷
却速度制御下において、より低温での圧延が可能となる
ため一層微細なベイナイト組織を達成できることによっ
て、降伏比、強度、加工性、靭性のいずれに対しても有
利となる。In other words, since it has the effect of significantly retarding ferrite and pearlite transformation, it is possible to improve the ultrafine bainite structure ratio, and it is possible to roll at a lower temperature under the control of the cooling rate during finish rolling, which will be described later. Therefore, by achieving a finer bainite structure, it is advantageous in terms of yield ratio, strength, workability, and toughness.
この効果を発揮させるためには0.05%以上が必要で
あるが、1.0%を越えると製造コストが徒らに上昇す
るばかりか変態が著しく遅延してマルテンサイト(MS
)相が生成され、加工性、靭性等に悪影響を与える。0.05% or more is required to exhibit this effect, but if it exceeds 1.0%, not only will manufacturing costs increase unnecessarily, but the transformation will be significantly delayed, resulting in martensite (MS).
) phase is generated, which adversely affects workability, toughness, etc.
A1:加工性、靭性の点から、主たる脱酸元素として使
用されるが、0.10%を越えて使用することは不必要
であるばかりでなく、かえってアルミナ系の介在物の増
加をもたらすため好ましくない。A1: From the viewpoint of workability and toughness, it is used as the main deoxidizing element, but its use in excess of 0.10% is not only unnecessary, but also causes an increase in alumina-based inclusions. Undesirable.
S:加工性、靭性、溶接性を向上させるためには可能な
限り低減させることが望ましいが、製造コストとの関連
もあり、商用鋼で比較的容易に達成でき、かつ実質的に
その悪影響を軽減可能な範囲として上限を0.020%
とする。S: It is desirable to reduce as much as possible in order to improve workability, toughness, and weldability, but it is also related to manufacturing costs, so it is relatively easy to achieve with commercial steel and it is possible to substantially reduce the negative effects. The upper limit is 0.020% as the range that can be reduced.
shall be.
Nb、V、Ti(X群):周知のごとく、これらのいず
れの元素もr粒の微細化作用が顕著であり、本発明にお
いても必要によりこの作用を利用することが可能である
。Nb, V, Ti (Group
しかしながら、添加量がこれら元素の合計で0.20%
を越えると前記効果は飽和するばかりでなく、析出硬化
による降伏比の上昇が著しくなって本発明の目的である
低降伏比を得る上で好ましくないので、上限を0.20
%とする必要がある。However, the total amount of these elements added is 0.20%.
If the value exceeds 0.20, the above effect not only becomes saturated, but also the yield ratio increases significantly due to precipitation hardening, which is not preferable for obtaining the low yield ratio that is the objective of the present invention.
It needs to be %.
Cr、Ni、Cu(Y群):固溶硬化元素として降伏比
を左程上昇させることなく強度向上を計り得ることおよ
びベイナイト変態温度を低下する作用のため極微細ベイ
ナイト組織を得易いこと等の効果を有するが、いずれも
高価な元素であるばかりか多量に添加すると加工性、靭
性、溶接性に悪影響があるので、これら元素の合計で1
.0%を上限とし、必要により添加すればよい。Cr, Ni, Cu (Y group): As solid solution hardening elements, it is possible to improve the strength without significantly increasing the yield ratio, and because it lowers the bainite transformation temperature, it is easy to obtain an extremely fine bainite structure. However, not only are these elements expensive, but adding them in large amounts has a negative effect on workability, toughness, and weldability.
.. The upper limit is 0%, and it may be added as necessary.
Zr、Mg、Ca、希土類元素(2群):鋼中硫化物の
形状制御に有効であり、適量の使用は機械的性質の異方
性を改善するので好ましいが、多量の添加は介在物量を
かえって増加させるので好ましくない。Zr, Mg, Ca, rare earth elements (group 2): Effective for controlling the shape of sulfides in steel, and using an appropriate amount is preferable because it improves the anisotropy of mechanical properties, but adding a large amount may reduce the amount of inclusions. This is not preferable because it actually increases the amount.
かかる悪影響の出ない範囲である元素合計量0.1%以
下において、必要により添加すればよい。They may be added as necessary within a total amount of elements of 0.1% or less, which is a range that does not cause such adverse effects.
B:微量の添加でフェライト・パーライト変態を遅延す
る効果があり、必要により0.020%以下に添加すれ
ばよい。B: Addition of a trace amount has the effect of delaying ferrite-pearlite transformation, and if necessary, it may be added in an amount of 0.020% or less.
次に、前記強化元素等を含有する鉄スラブを1000〜
1300℃で加熱する理由は、後続の処理工程における
効果を高めるためである。Next, the iron slab containing the above-mentioned strengthening elements etc.
The reason for heating at 1300° C. is to enhance the effect in subsequent treatment steps.
すなわち、本発明目的を達成するため、次工程の仕上圧
延工程では極微細ベイナイト組織を得る必要があるが、
そのためには鉄スラブ中における初期オーステナイト粒
は小さい方が好ましい。That is, in order to achieve the object of the present invention, it is necessary to obtain an extremely fine bainite structure in the next finish rolling process;
For this purpose, it is preferable that the initial austenite grains in the iron slab be small.
従って、スラブの加熱温度は低い方が望ましいが、10
00℃未満では所定の仕上圧延終了温度を確保できなく
なるので好ましくない。Therefore, it is desirable that the heating temperature of the slab be lower, but 10
If it is less than 00°C, it is not preferable because a predetermined finish rolling end temperature cannot be ensured.
一方、1300’Cを越える場合には、初期オーステナ
イト粒の粗大化に基因する整置を生じることおよび粗圧
延後に所定の仕上圧延開始温度を確保するに当り温度調
整を行なう必要を生じるので圧延能率の低下を来すこと
等のため望ましくない。On the other hand, if the temperature exceeds 1300'C, the initial austenite grains may become coarsened, resulting in misalignment, and it may be necessary to adjust the temperature to ensure a predetermined finish rolling start temperature after rough rolling, resulting in a reduction in rolling efficiency. This is undesirable as it may cause a decrease in
次に、仕上圧延条件およびその過程における冷却条件を
本発明範囲とする理由について述べる。Next, the reason why the finish rolling conditions and the cooling conditions in the process are within the scope of the present invention will be described.
既述したごと(、本発明目的にとって降伏比を実用上7
0%以下としかつ引張強度を高めることが要請されるが
、そのためには、本発明者等の検討による極微細ベイナ
イト組織率と降伏比の関係(第1図参照)や別途引張強
度と極微細ベイナイト組織率との関係はほぼ直線的な正
の関係にあるという知見等から、極微細ベイナイト組織
率を60%以上とする必要のあることが知られる。As already stated (for the purpose of the present invention, the yield ratio is practically 7
0% or less and to increase the tensile strength. To achieve this, the relationship between the ultrafine bainite structure ratio and the yield ratio (see Figure 1) and the relationship between the tensile strength and the ultrafine bainite structure, which have been studied by the present inventors, are required. From the knowledge that there is a substantially linear positive relationship with the bainite structure ratio, it is known that the ultrafine bainite structure ratio needs to be 60% or more.
そのためには、連続冷却変態曲線図(省略)からも明ら
かなように、まず第1にオースティナイト温度領域から
の冷却カーブが初析フェライト・パーライト変態ノーズ
を切らないような冷却速度すなわち臨界冷却速度以上の
急冷とすることが必要であり、第2にこの急冷を要する
温度範囲は、少くとも臨界冷却速度において初析フェラ
イト変態が開始する温度以上からベイナイト変態が開始
する温度以下までとすることが望ましいが、本発明にお
ける極微細ベイナイト組織は、加工歪が導入された微細
オーステナイト粒によってもたらされるものであり、そ
の変態特性は通常の熱処理によって得られるベイナイト
変態とは大巾に異なっているため、これを従来の変態曲
線図を用いて定量的に類推することは不可能である。In order to do this, as is clear from the continuous cooling transformation curve diagram (omitted), first of all, the cooling rate from the austinite temperature region does not cut the pro-eutectoid ferrite-pearlite transformation nose, that is, the critical cooling. It is necessary to perform rapid cooling at a rate higher than the cooling rate, and secondly, the temperature range that requires this rapid cooling must be from at least the temperature at which pro-eutectoid ferrite transformation begins to the temperature at which bainite transformation begins at the critical cooling rate. However, the ultrafine bainite structure in the present invention is produced by fine austenite grains to which processing strain has been introduced, and its transformation characteristics are vastly different from the bainite transformation obtained by ordinary heat treatment. , it is impossible to quantitatively infer this using conventional transformation curve diagrams.
従って、前記の定量推定を実施するためには、従来の変
態曲線図によらない新たなパラメータの導入が不可欠と
なる。Therefore, in order to carry out the quantitative estimation described above, it is essential to introduce new parameters that are not based on conventional transformation curve diagrams.
本発明者等は、鋭意検討の結果、既述の(1)〜(3)
式で示すTFS、TBSおよびVCを有効なパラメータ
として見出したものである。As a result of intensive study, the present inventors have determined that the above-mentioned (1) to (3)
TFS, TBS, and VC shown in the formula were found as effective parameters.
これらのパラメータは、各式からも明らかなように、主
として鋼の化学成分により規制されるが、その他にもス
ラブ加熱温度、仕上圧延温度、圧下率等の変化により影
響を受ける。As is clear from each equation, these parameters are mainly regulated by the chemical composition of the steel, but are also influenced by changes in the slab heating temperature, finish rolling temperature, rolling reduction, etc.
しかし、これらの影響は、本発明の処理条件内であれば
特に問題とする必要はない。However, these effects do not need to be a particular problem as long as the processing conditions of the present invention are met.
前記パラメータを使用し、本発明の条件下で仕上圧延お
よび冷却を実施することにより極微細ベイナイト組織率
60%以上を達成できる。By using the above parameters and performing finish rolling and cooling under the conditions of the present invention, an extremely fine bainite structure ratio of 60% or more can be achieved.
すなわち、第2図は、本発明に係る同一化学成分の鋼を
急冷終了温度はTBSに保って一定とし、冷却速度Vと
急冷開始温度(TI)を変化させた場合の極微細ベイナ
イト組織率の変化を模式的に示したものである。That is, Fig. 2 shows the ultrafine bainite structure percentage when the quenching end temperature of steel with the same chemical composition according to the present invention is kept constant at TBS, and the cooling rate V and quenching start temperature (TI) are varied. This diagram schematically shows the changes.
本図から明らかなように、いずれの冷却速度においても
、急冷開始温度が高くなるに従い極微細ベイナイト組織
率は上昇して急冷開始温度がTFSとほぼ同一となる温
度近傍で飽和する傾向となるが。As is clear from this figure, at any cooling rate, as the quenching start temperature increases, the ultrafine bainite structure rate increases and tends to be saturated near the temperature where the quenching start temperature is almost the same as TFS. .
飽和する極微細ベイナイト組織率の値は冷却速度が速い
もの程太きくなり、急冷開始温がTFS近傍ではv−■
cのときにほぼ60%に達することが確認される。The value of the saturated ultrafine bainite structure ratio increases as the cooling rate increases, and when the rapid cooling start temperature is near TFS, v-■
It is confirmed that it reaches approximately 60% when c.
次に、第3図は第2図と同一の鋼を急冷開始温度はTF
Sに保って一定とし、冷却速度Vと急冷終了温度(Tl
)を変化させた場合の極微細ベイナイト組織率の変化を
模式的に示1.たものである。Next, Figure 3 shows the same steel as in Figure 2, but the quenching start temperature is TF.
The cooling rate V and the quenching end temperature (Tl
) is schematically shown to show the change in ultrafine bainite structure ratio when changing 1. It is something that
本図から明らかなように、いずれの冷却速度においても
、急冷終了温度の低下とともに極微細ベイナイト組織率
は顕著に増加して急冷終了温度がTBSとほぼ同一とな
る温度近傍で飽和する傾向となる。As is clear from this figure, at any cooling rate, as the quenching end temperature decreases, the ultrafine bainite structure rate increases significantly, and tends to be saturated near the temperature where the quenching end temperature is almost the same as TBS. .
そして、この飽和時の値は、TBSの近傍において冷却
速度がVCより大きい場合には60%以上となるのに対
し、VCより小さい場合には60%を確保できないこと
が確認される。It is confirmed that this saturation value is 60% or more when the cooling rate is higher than VC in the vicinity of TBS, but 60% cannot be secured when it is lower than VC.
以−Fのことより、本発明において冷却をTFS〜TB
Sの温度範囲内にてvc以トの冷却速度で実施する理由
が理解される。From the above, in the present invention, cooling is performed from TFS to TB.
The reason for carrying out the cooling rate below vc within the temperature range of S is understood.
次に、前記冷却の前工程である仕上圧延について説明す
るに、仕上圧延開始温度の上限を950℃とする理由は
、これを越えると未再結晶温度領域での圧下が不十分と
なって加工歪の導入不良による比較的粗大なベイナイト
組織が混在するよめになり、加工性、靭性な劣化させる
ためである。Next, to explain the finish rolling, which is a pre-cooling step, the reason why the upper limit of the finish rolling start temperature is set at 950°C is that if it exceeds this, the reduction in the non-recrystallization temperature region becomes insufficient, resulting in This is because poor introduction of strain results in a relatively coarse bainite structure mixed in, which deteriorates workability and toughness.
また、仕上圧延終了温度をTFS以上とする理由は、こ
れより低温域では、通常の圧延法によると2相部度領域
(r+a)で圧下な受けることとなり、加工性および靭
性の劣化を生し易いからである。In addition, the reason why the finish rolling end temperature is set to be higher than TFS is that in a lower temperature range, under normal rolling method, rolling will be applied in the two-phase region (r+a), resulting in deterioration of workability and toughness. This is because it is easy.
しかしながら、本発明の化学成分、圧延条件下の処理で
は何らの制御を行なわない限り仕上圧延終了温度はTF
S以下となるので、これを避けるため、仕上圧延中にお
いても冷却速度制御を行って仕上圧延終了温度をTFS
以上に保つことが必要である。However, in the treatment under the chemical composition and rolling conditions of the present invention, unless any control is performed, the finish rolling end temperature will be TF
In order to avoid this, the cooling rate is controlled even during finish rolling to keep the finish rolling end temperature at TFS.
It is necessary to maintain the above level.
仕上圧延中の合計圧下率は、十分に均一な極微細ベイナ
イト組織を得るために少くとも50%以上とする必要が
ある。The total rolling reduction during finish rolling needs to be at least 50% or more in order to obtain a sufficiently uniform ultrafine bainite structure.
次に、最終工程である巻取について述べる。Next, the final process, winding, will be described.
前記により冷却された後の鋼の熱履歴は、出来る限り等
温変態的に極微細ベイナイト組織が生成される状態が好
ましいので、例えば熱延ホットストリップミルのごとく
巻取工程においてこの熱履歴を得易い場合は好都合であ
る。The thermal history of the steel after being cooled by the above method is preferably such that an extremely fine bainite structure is generated through isothermal transformation as much as possible, so this thermal history can be easily obtained in a winding process such as in a hot rolling hot strip mill, for example. The case is favorable.
しかしながら、本発明のように、フェライト・パーライ
ト変態温度領域を急冷してその進行を極力抑制するよう
な冷却条件とした場合には、巻取後に急激に変態が生じ
、その変態潜熱によりコイル温度が上昇して極微細ベイ
ナイト変態温度範囲を越えてパーライト変態温度領域ま
で達することがある。However, as in the present invention, when the cooling conditions are set such that the ferrite/pearlite transformation temperature region is rapidly cooled and its progress is suppressed as much as possible, transformation occurs rapidly after winding, and the coil temperature increases due to the latent heat of transformation. It may rise to exceed the extremely fine bainite transformation temperature range and reach the pearlite transformation temperature range.
かかる場合には、極微細ベイナイト組織率が低下するの
で、強度の低下、降伏比の上昇が著しくなり、目的とす
る機械的性質を確保できない場合がある。In such a case, the percentage of ultrafine bainite structure decreases, resulting in a significant decrease in strength and increase in yield ratio, and it may not be possible to secure the desired mechanical properties.
この巻取後の変態潜熱による温度上昇の影響は、本発明
の化学成分範囲であれば、巻取温度を(TBS−30℃
)以下とすることによって解消することができる。The effect of temperature rise due to latent heat of transformation after winding is that if the chemical composition is within the range of the present invention, the winding temperature is (TBS - 30℃
) This can be resolved by doing the following.
一方、巻取温度をMS点以上とする理由は、しからざる
場合には、部分的にマルテンサイト相が混合する危険が
あるためである。On the other hand, the reason why the winding temperature is set to be higher than the MS point is that there is a risk that the martensitic phase may be partially mixed if it is not done.
本発明の圧延条件下では、オーステナイト粒が十分に微
細化されているため、マルテンサイト相の割合が10%
未満であれば材質を大きく損うことはないが、これを越
えると加工性、靭性に悪影響を生じ、特に多量に混入す
ると鋼板形状の不良化原因にもなるので、いずれにして
もマルテンサイト相の混入はできる限り避けるべきであ
る。Under the rolling conditions of the present invention, the austenite grains are sufficiently refined, so that the proportion of martensite phase is 10%.
If it is less than this, the material quality will not be significantly damaged, but if it exceeds this, it will have a negative effect on workability and toughness, and if it is mixed in a particularly large amount, it can cause defects in the shape of the steel sheet, so in any case, martensitic phase Contamination should be avoided as much as possible.
実施例
第1表に示す化学成分の各種鉄スラブ(実施例1〜10
、比較例1〜4)を同表に示す圧延条件で処理して板厚
6龍の熱延鋼板を得、これらの機械的特性値を求めたと
ころ第2表の結果を得た。Examples Various iron slabs with chemical components shown in Table 1 (Examples 1 to 10)
, Comparative Examples 1 to 4) were processed under the rolling conditions shown in the same table to obtain hot-rolled steel sheets with a thickness of 6 mm, and their mechanical property values were determined, and the results shown in Table 2 were obtained.
第2表から明らかなように、本実施例のものは引張強度
(TS)が高い(特に実施例5〜10)にもかかわらず
、0.2%耐力(実質的に降伏点と見做し得る)は相対
的に低い(従って、降伏比は実用範囲の70%以下であ
る)ことの他、強度と伸び(El)とのバランスが良く
、衝撃性、加工性、溶接性の点でも極めてすぐれている
ことが理解される。As is clear from Table 2, although the tensile strength (TS) of the present examples is high (especially Examples 5 to 10), the yield strength is 0.2% (which is essentially considered as the yield point). In addition to being relatively low (therefore, the yield ratio is less than 70% of the practical range), it has a good balance between strength and elongation (El), and is extremely good in terms of impact resistance, workability, and weldability. It is understood that it is excellent.
これに対し、従来法による比較例のうち、仕上圧延過程
における冷却速度が遅い場合(比較例1)および巻取温
度が高い場合(比較例2)では、抗張力が極めて低いた
め降伏比も著しく高いが、これは極微細ベイナイトの生
成がいずれも不十分なためと云える。On the other hand, among the comparative examples using the conventional method, when the cooling rate in the finish rolling process is slow (Comparative Example 1) and when the coiling temperature is high (Comparative Example 2), the tensile strength is extremely low and the yield ratio is also extremely high. However, this can be said to be due to insufficient formation of ultrafine bainite.
また、仕上圧延開始温度を通常圧延法と同程度に高くし
た場合(比較例3)では、他の条件が本発明条件に適合
していても伸び、衝撃特性例である吸収エネルギ(E−
20℃)と遷移温度(vVrs)、加工特性例である切
欠き伸びがともに著しく悪化する。In addition, when the finish rolling start temperature is set to be as high as that in the normal rolling method (Comparative Example 3), even if other conditions meet the conditions of the present invention, elongation occurs, and the absorbed energy (E-
20° C.), transition temperature (vVrs), and notch elongation, which is an example of processing characteristics, are both significantly deteriorated.
これは、1粒の微細化が不充分となり、粗大なベイナイ
ト組織が形成されたことに起因するものと考えられる。This is considered to be due to insufficient refinement of one grain and the formation of a coarse bainite structure.
以上から明らかなように、従来例によるときは引張特性
、特に引張強度と降伏比や衝撃特性を総合した意味での
靭性、加工性および溶接性の向上を同時に達成すること
は不可能であるが、本実施例によればこれが可能となる
。As is clear from the above, when using conventional methods, it is impossible to simultaneously achieve improvements in tensile properties, especially in the comprehensive sense of tensile strength, yield ratio, and impact properties, toughness, workability, and weldability. , this is possible according to this embodiment.
本実施例により得られる熱延鋼帯は、降伏比の上限が規
制されている鋼材の用途、例えばラインパイプ、ケーシ
ングパイプを始めとする各種の加工用途に適する。The hot-rolled steel strip obtained in this example is suitable for various processing applications including steel materials whose upper limit of yield ratio is regulated, such as line pipes and casing pipes.
以上説明した通り、本発明によれば、(1)すぐれた特
性の銅帯を単に熱延のみで製造できる上に、得られる銅
帯団2)低降伏比であるため高強度鋼であっても加工が
容易である、(3)特に低歪領域の加工時に有利である
、(4)強化機構として組織強化を利用しているが、加
工熱処理的手法に従っているため強度に対する加工性、
靭性のバランスが良い、(5)低い合金元素含有量にも
かかわらず高強度を得ることができるので、溶接性にす
ぐれている等の種々の効果が得られる。As explained above, according to the present invention, (1) a copper strip with excellent properties can be produced simply by hot rolling, and the resulting copper strip (2) is a high-strength steel with a low yield ratio. (3) It is especially advantageous when processing low strain areas; (4) Although it uses structural reinforcement as a strengthening mechanism, it follows a processing heat treatment method, so it has low workability in terms of strength.
Various effects can be obtained, such as a good balance of toughness and (5) high strength despite low alloying element content, resulting in excellent weldability.
第1図は、降伏比と極微細ベイナイト組織率の関係を説
明する図、第2図は極微細ベイナイト組織率におよぼす
急冷開始温度と冷却速度の影響を説明する図、第3図※
場微細ベイナイト率におよぼす急冷終了温度と冷却速度
の影響を説明する図である。Figure 1 is a diagram explaining the relationship between the yield ratio and the ultra-fine bainite structure ratio, Figure 2 is a diagram explaining the influence of the rapid cooling start temperature and cooling rate on the ultra-fine bainite structure ratio, and Figure 3 *
FIG. 3 is a diagram illustrating the influence of the quenching end temperature and cooling rate on the field fine bainite fraction.
Claims (1)
、該強化元素等の含有量をC:0.02〜0.12%(
重量、以下同じ)、Mn:1.0〜2.0%、Si:1
.0%以下、Mo:0−05〜1−0%、Al:0.1
0%以下、S:0.020%以下にそれぞれ保ち、かつ
前記熱間圧延に当り、前記スラブの加熱を1000〜1
300℃で、仕上圧延を950℃以下の開始温度である
が、後記TFS以上の終了温度にてかつ合計圧下率50
%以上で、冷却を前記TFS〜後記TBSの温度範囲内
にて後記VC以上の冷却速度でおよび巻取を鋼のMS点
〜(TBS−30℃)の温度範囲内で順次行な、う〔た
だし、TFS(準平衛状態における初析フェライト変態
開始温度℃)−一204〔%C)−14(%Mn)+5
8C%5i)−23C%Ni)+24〔%Cr)+22
C%Mo)−14(%Cu)+(0,8−(%C〕)・
(−75〔%Mnl+47〔%5i)−30(%Cr)
+20C%Mo)−8,8C%Cu:l)+910、T
BS(極微細ベイトナイト変態の開始温度℃)=−15
8〔%C〕−11〔%Mn〕+35(%Si、)l−1
7C%Ni〕−25〔%Cr〕−19〔%Mo)、vc
(極微細ベイトナイト組成率を60%以上とするために
必要な冷却速度の下限、℃/5)−12−3(%C〕−
S、SC%Mn)+13.2(%5i)−4,7〔%N
1)−19,5(%Cr)+25exp(−2,5〔%
Mo))−6,6(%Cu)+15)ことを特徴とする
加工用非調質高張力熱延銅帯の製造方法。 2特許請求の範囲第1項において、強化元素等としてさ
らにNb、V、TiからなるX群から選ばれる1種以上
の元素を0.2%以下および(または)Cr、Ni、C
uからなるY群から選ばれる1種以上の元素を1.0%
以下および(または)Zr、Ca、Mg、希土類元素か
らなる2群から選ばれる1種以上の元素を0.1%以下
および(または)Bを0.020%以下含有せしめたこ
とを特徴とする加工用非調質高張力熱延銅帯の製造方法
。[Claims] 1. When hot rolling an iron slab containing reinforcing elements, etc., the content of the reinforcing elements, etc. is changed to C: 0.02 to 0.12% (
weight, the same below), Mn: 1.0 to 2.0%, Si: 1
.. 0% or less, Mo: 0-05 to 1-0%, Al: 0.1
0% or less and S: 0.020% or less, and during the hot rolling, the slab was heated to 1000 to 1
Finish rolling at 300°C, with a starting temperature of 950°C or lower, but with a finishing temperature of TFS or higher, and a total rolling reduction of 50°C.
% or more, cooling is performed sequentially within the temperature range of TFS to TBS described below at a cooling rate of VC or higher, and winding is performed within the temperature range of the MS point of the steel to (TBS - 30 ° C.). However, TFS (temperature at which pro-eutectoid ferrite transformation starts in semi-normal state °C) - -204 [%C] -14 (%Mn) +5
8C%5i)-23C%Ni)+24[%Cr)+22
C%Mo)-14(%Cu)+(0,8-(%C))・
(-75[%Mnl+47[%5i)-30(%Cr)
+20C%Mo)-8,8C%Cu:l)+910,T
BS (starting temperature of ultrafine baitonite transformation °C) = -15
8[%C]-11[%Mn]+35(%Si,)l-1
7C%Ni]-25[%Cr]-19[%Mo), vc
(Lower limit of cooling rate required to make ultrafine baitotonite composition ratio 60% or more, °C/5) -12-3 (%C] -
S, SC%Mn)+13.2(%5i)-4,7[%N
1) -19,5(%Cr)+25exp(-2,5[%
Mo)) -6,6 (% Cu) + 15) A method for producing a non-thermal high tensile strength hot rolled copper strip for processing. 2 In claim 1, it is further provided that 0.2% or less of one or more elements selected from group X consisting of Nb, V, and Ti as reinforcing elements and/or Cr, Ni, and C
1.0% of one or more elements selected from the Y group consisting of u
It is characterized by containing 0.1% or less of one or more elements selected from the following and/or two groups consisting of Zr, Ca, Mg, and rare earth elements and/or 0.020% or less of B. A method for producing a non-tempered high tensile strength hot rolled copper strip for processing.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4241178A JPS58733B2 (en) | 1978-04-11 | 1978-04-11 | Method for manufacturing non-temperature high tensile strength hot rolled steel strip for processing |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4241178A JPS58733B2 (en) | 1978-04-11 | 1978-04-11 | Method for manufacturing non-temperature high tensile strength hot rolled steel strip for processing |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS54134019A JPS54134019A (en) | 1979-10-18 |
| JPS58733B2 true JPS58733B2 (en) | 1983-01-07 |
Family
ID=12635316
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4241178A Expired JPS58733B2 (en) | 1978-04-11 | 1978-04-11 | Method for manufacturing non-temperature high tensile strength hot rolled steel strip for processing |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS58733B2 (en) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4472208A (en) * | 1982-06-28 | 1984-09-18 | Sumitomo Metal Industries, Ltd. | Hot-rolled high tensile titanium steel plates and production thereof |
| JPH0772323B2 (en) * | 1985-04-15 | 1995-08-02 | 株式会社神戸製鋼所 | Non-heat treated steel bar for hot forging |
| JP2515173B2 (en) * | 1990-09-28 | 1996-07-10 | 愛知製鋼株式会社 | High strength, high toughness non-heat treated steel for forging |
| EP0730042B1 (en) * | 1994-09-20 | 2002-12-11 | Kawasaki Steel Corporation | Bainite steel material of little scatter of quality and method of manufacturing the same |
-
1978
- 1978-04-11 JP JP4241178A patent/JPS58733B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS54134019A (en) | 1979-10-18 |
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