JPH0120210B2 - - Google Patents
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- Publication number
- JPH0120210B2 JPH0120210B2 JP58177701A JP17770183A JPH0120210B2 JP H0120210 B2 JPH0120210 B2 JP H0120210B2 JP 58177701 A JP58177701 A JP 58177701A JP 17770183 A JP17770183 A JP 17770183A JP H0120210 B2 JPH0120210 B2 JP H0120210B2
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Classifications
-
- 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
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
-
- 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
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/001—Heat treatment of ferrous alloys containing Ni
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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)
- Heat Treatment Of Strip Materials And Filament Materials (AREA)
Description
この発明は、降伏点:90Kgf/mm2以上、引張強
さ:97Kgf/mm2以上、衝撃破面遷移温度:−60℃以
下の高強度高靭性鋼材の製造方法、特に前記特性
を備えた板厚:40〜150mmの高張力鋼板をも安定
して製造し得る方法に関するものである。
近年、各種鋼構造物は大型化の一途をたどつて
おり、これにともない使用される高張力鋼板は
益々高強度化される傾向があり、例えば、揚水発
電所の水圧鉄管には180mm厚のHT80鋼板(引張
強さ:80Kgf/mm2以上を目安とするもの)が使用さ
れるに至つている。
しかしながら、現在、この種の構造物には、引
張強さ:60Kgf/mm2以上を目安とするHT60鋼板
や、前記HT80鋼板が使用に供されてはいるもの
の、降伏点:90Kgf/mm2以上、引張強さ:97Kgf/mm2
以上の高強度を有するHT100級鋼板の使用に踏
み切れないでいるのが現状であつた。なぜなら、
板厚:40mm以上の厚鋼板について、降伏点:
90Kgf/mm2以上、引張強さ:97Kgf/mm2以上の高強
度を得ることが極めて困難であること、
前記所定の強度と同時に、衝撃破面遷移温
度:−60℃以下という優れた低温靭性を鋼材に
満足せしめることが極めて困難であること、
更に、実際の構造物施工上何ら問題ないだけ
の溶接性を上述のような高強度鋼に付与するこ
とが難かしいこと、
等のような問題を解決できないからであつた。
ところで、従来試作されているHT100鋼材は、
主として板厚:20〜40mmの鋼板であり、強度を確
保するためにCを0.15%以上、或いはVを0.06%
以上含有しており、このため母材靭性に劣る上
(衝撃破面遷移温度:−40℃以上)、溶接性につい
ても十分に配慮されているとは言い難いものであ
つた。しかも、板厚を100mm程度に増加させるた
めには、焼入れ性を従来以上に増加させる必要が
あり、必然的に合金元素の添加量を増加せざるを
得ないという事情が生ずるが、単純に合金元素量
を増加させるだけでは母材靭性や溶接性の更なる
劣化を招くという問題を免れることができなかつ
たのである。
本発明者等は、上述のような観点から、溶接構
造物部材として使用できるだけの靭性値(衝撃破
面遷移温度:−60℃以下)と溶接性〔溶接割れ感
受性指数(PcM)が0.31%以下:但し、PcMは、
式、
PcM=C(%)+Si(%)/30+Mn(%)/20
+Cu(%)/20+Ni(%)/60+Cr(%)/20
+Mo(%)/15+V(%)/10+5×B(%)
で表わされるものであり、以下、成分割合を表わ
す%は重量%とする〕とを備え、更に構造物の大
型化に対応できるだけの肉厚(40mm〜150mm)を
有するHT100鋼材を提供すべく、特に、従来の
高張力鋼における微量元素の影響に着目して研究
を行つた結果、以下(a)〜(e)に示される如き知見を
得るに至つたのである。即ち、
(a) 従来の高張力鋼は、通常、0.008〜0.015%程
度のNを不純物として含有しているが、このN
含有量を、特に0.0040%以下という低い値にま
で低減すると鋼の焼入れ性が一段と向上し、合
金成分を多量に添加することなくマルテンサイ
トとベイナイトとの混合組織を容易に得られる
ようになること、
(b) 鋼中のN含有量を0.0040%以下に低減する
と、微量のV添加で十分な析出強化を得ること
ができ、このためVの添加量を0.06%以下に制
限することが可能となつて、析出強化による母
材靭性の劣化、溶接性の劣化を抑制できるこ
と、
(c) 更に、P含有量を0.008%以下に下げ、かつ
焼入れ処理に続いて、所定温度に加熱保持した
後の冷却を水冷とした焼もどし処理を施すと、
従来の焼もどし温度よりも低い焼もどし温度で
あつても十分に満足し得る低温靭性を備えた鋼
材が得られること、
(d) また、従来の高張力鋼は、脱酸及び焼もどし
軟化抵抗を付与することを目的として0.3%程
度のSiを含有しているが、このSi含有量を、特
に0.15%以下にすると焼入れの際に微量のベイ
ナイトが生成することとなり、低温靭性が大幅
に向上すること、
(e) このように、鋼中のN量を低減し、更にSi、
P及びSの含有量をも低く抑え、かつ微量のV
とBを添加した上で、これに焼入れ処理と、所
定温度に加熱後水冷するという焼もどし処理と
を施すと、例え肉厚が40mmを越えるものであつ
ても、強度と靭性に優れ、かつ良好な溶接性を
備えた100Kgf/mm2級高張力鋼材が安定して得ら
れること。
この発明は、上記知見に基づいてなされたもの
であり、
C:0.07〜0.15%、Si:0.15%以下、
Mn:0.40〜1.00%、Cr:0.40〜1.20%、
Ni:2.0〜4.2%、Mo:0.40〜0.80%、
V:0.01〜0.06%、
B:0.0004〜0.0015%、
Cu:0.50%以下、
Sol.Al:0.010〜0.100%、
P:0.008%以下、S:0.003%以下、
N:0.0040%以下、
Fe及びその他の不可避不純物:残り、
から成り、かつ溶接割れ感受性指数(PcM)が
0.31%以下である成分組成範囲を有し、板厚:40
mm〜150mmの鋼板を、〔Ac3変態点〜1000℃〕の温
度域に加熱後、焼入れし、次いで560〜630℃に加
熱後水冷するという焼もどし処理を施すことによ
り、優れた靭性と高強度を備え、かつ溶接性の良
好な、40mm〜150mmの肉厚のものをも含む高張力
鋼材を安定して製造する点に特徴を有するもので
ある。
次いで、この発明の方法において、鋼の化学成
分組成及び熱処理条件を上記のように数値限定し
た理由を説明する。
A 鋼の化学成分組成
a) C
C成分には、鋼の焼入れ性と強度を確保す
る作用があるが、その含有量が0.07%未満で
は前記作用に所望の効果を得ることができ
ず、他方0.15%を越えて含有させると溶接
性、特に低温割れ性を著しく劣化させること
から、C含有量を0.07〜0.15%と定めた。
b) Si
Siは、通常、鋼の脱酸と強度確保のために
0.3%程度添加されるものであるが、この発
明の方法においてはSi含有量を0.15%以下に
制限する点に特徴があり、これによつてベイ
ナイトの生成を促進し、マルテンサイトとベ
イナイトの混合組織を得て鋼材の靭性を向上
させるものである。そして、Si含有量が0.15
%を越えると前記ベイナイト生成促進効果が
減少することから、Si含有量を0.15%以下と
定めた。
なお、Si含有量の下限は格別に定める必要
がなく、少ないほど良好な効果が得られる
が、製鋼の容易さを考慮すれば0.01%程度に
まで低減するのを限度とすることが好まし
い。
c) Mn
Mn成分には、鋼の焼入れ性を確保する作
用があるが、その含有量が0.40%未満では前
記作用に所望の効果が得られず、他方1.00%
を越えて含有させると靭性並びに溶接性を劣
化するようになることから、Mn含有量を
0.40〜1.00%と定めた。
d) Cr
Cr成分は、焼入れ性と強度を確保するた
めに0.40%以上含有させるが、1.20%を越え
て含有させると靭性を劣化するようになるこ
とから、Cr含有量を0.40〜1.20%と定めた。
e) Ni
Ni成分には、焼入れ性の確保と低温靭性
向上作用があるので2.0%以上含有せしめる
が、経済性を考慮してその上限を4.2%と定
めた。なお、Niは靭性を低下させることな
く焼入れ性を増加できる元素であり、40〜
150mm厚のHT100鋼板を製造するためには2.7
%以上の量で含有させることが望ましい。
f) Mo
Mo成分には、鋼の焼入れ性を増大させ、
かつ焼もどし軟化抵抗を高めてその強度上昇
を達成する作用があるが、その含有量が0.40
%未満では前記作用に所望の効果が得られ
ず、他方0.80%を越えて含有させると溶接性
を著しく劣化させることから、Mo含有量を
0.40〜0.80%と定めた。
g) V
V成分には、析出強化により強度を増加さ
せる作用があり、所望の強度を確保するため
に0.01%以上含有せしめるものであるが、
0.06%を越えて含有させると靭性及び溶接性
を劣化するようになることから、V含有量を
0.01〜0.06%と定めた。
なお、本発明の方法においては、N含有量
を0.004%以下と低く抑えていること、また
低温焼もどしを行うことにより、微量のV添
加で十分な強度を確保できるので、V含有量
を0.01〜0.04%に調整することが靭性確保上
最も望ましい。
h) B
B成分は、微量添加で鋼の焼入れ性を大幅
に向上できるので0.0004%以上含有せしめる
ものであるが、0.0015%を越えて含有せしめ
ると靭性が劣化するようになることから、B
含有量を0.0004〜0.0015%と定めた。なお、
本発明の方法においてはN含有量を0.0040%
以下と低く抑えているので、B含有量は
0.0004〜0.0010%の範囲が望ましい。
i) Cu
Cu成分には、鋼の強度、靭性、耐食性を
向上させる作用があるが、0.50%を越えて含
有させると熱間加工性、靭性、或いは溶接時
の高温割れ性を劣化するようになることか
ら、Cu含有量を0.50%以下と定めた。なお、
Cu含有量が微量であつてその添加効果は認
められるが、顕著な効果を得るためには0.05
%以上のCuを含有させることが望ましい。
j) Sol.Al
Sol.Al成分には、鋼の脱酸作用と、B成分
の焼入れ性向上効果を増加させる作用がある
が、その含有量が0.010%未満では前記作用
に所望の効果が得られず、他方0.100%を越
えて含有させると靭性を劣化するようになる
ことから、Sol.Al含有量を0.010〜0.100%と
定めた。
k) P、及びS
これらの不純物は、鋼の靭性向上のために
は可能な限り低減することが望ましい。
焼入れ・焼もどしによつて鋼に降伏強さ:
90Kgf/mm2以上、引張強さ:97Kgf/mm2以上を満
足させるためには、低温で焼戻すことが好ま
しいが、このときP含有量が0.008%を越え
て高いと焼もどし脆性によつて靭性が大幅に
低下することとなる。従つて、P含有量を
0.008%以下と定めた。
また、S含有量が0.003%を越えて増加す
ると粗大なMnSを生成し、これが圧延時に
伸長されて靭性の劣化を招くことから、S含
有量を0.003%以下と定めた。
l) N
Nを0.0040%未満にすることは、鋼の焼入
れ性を高め、母材の強度と靭性向上に極めて
有効な手段である。即ち、N含有量を0.0040
%以下とし、Sol.Al含有量を0.01〜0.10%に
調整することにより、固溶B量を0.0003ppm
以上とすることができ、焼入れ性が向上する
のである。また、N量が低いためにAlNの
粗大化が抑制され、靭性が向上する。更に、
低N化によつてVNの生成が抑制されるた
め、通常のオーステナイト化温度でVが均一
固溶するので、Vの添加量を制限できる効果
もある。
このようなことから、N含有量を0.0040%
以下と定めた。
m) PcM(溶接割れ感受性指数)
溶接時に、十分に高い温度で予熱を行つた
としても、式
PcM(%)=C(%)+Si(%)/30
+Mn(%)/20+Cu(%)/20+Ni(%)/60
+Cr(%)/20+Mo(%)/15+V(%)/10
+5×B(%)
で表わされるPcM(溶接割れ感受性指数)が
0.31%を越えていると低温割れ発生率が極め
て高くなり、十分な溶接性を確保できなくな
ることから、PcMを0.31%以下と定めた。
B 熱処理条件
a) 焼入れ前の加熱温度
焼入れ前の加熱温度をAc3変態点以上とす
るのは、鋼を完全にオーステナイト化して合
金元素を均一に固溶させるためであり、Ac3
変態点以下の加熱では合金元素を均一固溶さ
せることができない。一方、該加熱温度が
1000℃を越えると、オーステナイト結晶粒が
粗大化して靭性低下を来たすようになること
から、焼入れ前の加熱温度を〔Ac3変態点〜
1000℃〕と定めた。
b) 焼もどし温度
560℃以上の温度で焼もどすのは、焼入れ
により導入された歪みを除去し、かつ炭化物
を微細に析出して強度及び靭性を向上させる
理由からであり、焼もどし温度が560℃未満
では前記効果を得ることができない。一方、
焼もどし温度が630℃を越えると、鋼材強度
が低下して、降伏強さ:90Kgf/mm2以上、引張
強さ:97Kgf/mm2以上を満足しなくなることか
ら、焼もどし温度を560〜630℃と定めた。
なお、鋼材を焼もどし温度に加熱・保持し
た後水冷することは本発明方法の特徴の1つ
であるが、このような処理によつて低温靭性
を著しく向上することができるのである。こ
れは、例えば40mmを越えるような肉厚の鋼材
では焼もどし後の冷却速度が低下し、焼もど
し脆性の感受性が高まるものであるが、焼も
どし温度に加熱・保持した後に水冷を実施し
て冷却速度:0.5〜6.0℃/secを確保すると、
前記不都合が解消されるとの理由によるもの
である。
また、この発明の方法は、板厚:40mm〜
150mmの高張力厚肉鋼板の製造において特に
顕著な効果を発揮するものである。なぜな
ら、40mm未満の肉厚の鋼材では、合金元素を
多量に添加しなくても母材の強度と靭性を比
較的容易に確保できるからである。
また板厚が150mmを越えると水冷の効果が
得られなくなる。
次に、この発明を実施例により比較例と対比し
ながら説明する。
実施例
まず、第1表に示す如き化学成分組成の本発明
対象鋼A〜F、及び比較鋼G〜Iを溶製した。
次いで、これを熱間鍛造によつて150mm厚のス
ラブとし、続いて熱間圧延によつて100mm厚の鋼
板とした。このときの圧延加熱温度は1150℃であ
つた。
次に、得られた100mm厚の鋼板を、第2表に示
されるように920℃に再加熱した後、水焼入れを
行い、引続いて580℃、或いは600℃に加熱して1
時間保持した後水冷するという焼もどしを施し
た。
また、これとは別に、本発明対象鋼A〜Fにつ
いては、前記と同様に焼入れしたものに、600℃
に1時間加熱保持した後空冷するという従来の
This invention relates to a method for producing a high-strength, high-toughness steel material having a yield point of 90 Kgf/mm 2 or more, a tensile strength of 97 Kgf/mm 2 or more, and an impact fracture transition temperature of -60°C or less, and in particular a plate having the above characteristics. The present invention relates to a method that can stably produce high-strength steel plates having a thickness of 40 to 150 mm. In recent years, various steel structures have become larger and larger, and the high-tensile steel plates used are becoming increasingly stronger. HT80 steel plates (with a tensile strength of 80Kgf/mm2 or higher as a guide) are now being used. However, although HT60 steel plates and the aforementioned HT80 steel plates, which have a tensile strength of 60 Kgf/mm 2 or higher, are currently used in this type of structure, they have a yield point of 90 Kgf/mm 2 or higher. , Tensile strength: 97Kgf/ mm2
At present, it has not been possible to use HT100 grade steel sheets, which have such high strength. This is because, for thick steel plates with a plate thickness of 40 mm or more, the yield point is:
It is extremely difficult to obtain a high strength of 90 Kgf/mm 2 or more, tensile strength: 97 Kgf/mm 2 or more, and at the same time, it has excellent low-temperature toughness with an impact fracture transition temperature of -60°C or less. It is extremely difficult to make steel materials satisfy these requirements, and furthermore, it is difficult to give the above-mentioned high-strength steel enough weldability to cause no problems when constructing actual structures. This was because the problem could not be resolved. By the way, the HT100 steel material that has been prototyped so far,
It is mainly a steel plate with a thickness of 20 to 40 mm, and contains 0.15% or more of C or 0.06% of V to ensure strength.
Therefore, not only is the toughness of the base material inferior (impact fracture surface transition temperature: -40°C or higher), but also it cannot be said that sufficient consideration has been given to weldability. Moreover, in order to increase the plate thickness to about 100 mm, it is necessary to increase the hardenability more than before, which inevitably necessitates an increase in the amount of alloying elements added. Simply increasing the amount of elements could not avoid the problem of further deterioration of base metal toughness and weldability. From the above-mentioned viewpoints, the present inventors have developed a material with a toughness value (impact fracture transition temperature: -60°C or less) and weldability [weld cracking susceptibility index (PcM) of 0.31% or less] that can be used as a welded structure member. :However, PcM is
Formula, PcM=C (%) + Si (%) / 30 + Mn (%) / 20 + Cu (%) / 20 + Ni (%) / 60 + Cr (%) / 20 + Mo (%) / 15 + V (%) / 10 + 5 × B (%) ), and hereinafter, % representing the component proportion is expressed as weight %]. In particular, as a result of research focusing on the influence of trace elements on conventional high-strength steel, we have obtained the findings shown in (a) to (e) below. That is, (a) Conventional high-strength steel usually contains about 0.008 to 0.015% N as an impurity;
If the content is reduced to a low value, especially 0.0040% or less, the hardenability of the steel will further improve, and a mixed structure of martensite and bainite can be easily obtained without adding large amounts of alloying components. (b) When the N content in steel is reduced to 0.0040% or less, sufficient precipitation strengthening can be obtained with the addition of a small amount of V, and therefore it is possible to limit the amount of V added to 0.06% or less. (c) In addition, after the P content is lowered to 0.008% or less and after being heated and held at a specified temperature following quenching treatment, When tempering is performed using water cooling,
(d) In addition, conventional high-strength steel has low deoxidation and tempering softening resistance. It contains about 0.3% Si for the purpose of imparting the same properties, but if this Si content is reduced to 0.15% or less, a small amount of bainite will be generated during quenching, which will significantly improve low-temperature toughness. (e) In this way, the amount of N in the steel is reduced and further Si,
The content of P and S is kept low, and a trace amount of V
By adding B and B, and then subjecting it to quenching and tempering, which involves heating to a predetermined temperature and cooling with water, even if the wall thickness exceeds 40 mm, it will have excellent strength and toughness, and 100Kgf/mm class 2 high tensile strength steel with good weldability can be stably obtained. This invention was made based on the above findings, and includes C: 0.07 to 0.15%, Si: 0.15% or less, Mn: 0.40 to 1.00%, Cr: 0.40 to 1.20%, Ni: 2.0 to 4.2%, Mo : 0.40 to 0.80%, V: 0.01 to 0.06%, B: 0.0004 to 0.0015%, Cu: 0.50% or less, Sol.Al: 0.010 to 0.100%, P: 0.008% or less, S: 0.003% or less, N: 0.0040 % or less, Fe and other unavoidable impurities: remaining, and the weld cracking susceptibility index (PcM) is
It has a component composition range of 0.31% or less, plate thickness: 40
mm~150mm steel plate is heated to a temperature range of [Ac 3 transformation point ~1000℃], quenched, then heated to 560~630℃, and then water-cooled to achieve excellent toughness and high It is characterized by the stable production of high-strength steel materials, including those with wall thicknesses of 40 mm to 150 mm, that have strength and good weldability. Next, the reason why the chemical composition and heat treatment conditions of the steel are numerically limited as described above in the method of the present invention will be explained. A Chemical composition of steel a) C The C component has the effect of ensuring the hardenability and strength of steel, but if its content is less than 0.07%, the desired effect cannot be obtained, and on the other hand If the C content exceeds 0.15%, the weldability, especially the cold crackability, will be significantly deteriorated, so the C content was set at 0.07 to 0.15%. b) Si Si is usually used to deoxidize steel and ensure strength.
The method of this invention is characterized by limiting the Si content to 0.15% or less, which promotes the formation of bainite and improves the mixing of martensite and bainite. It improves the toughness of steel by obtaining a structure. And the Si content is 0.15
If the Si content exceeds 0.15%, the effect of promoting bainite formation decreases, so the Si content was set at 0.15% or less. Note that there is no need to set a lower limit for the Si content; the lower the Si content, the better the effect. However, in consideration of ease of steel manufacturing, it is preferable to reduce the Si content to about 0.01%. c) Mn The Mn component has the effect of ensuring the hardenability of steel, but if its content is less than 0.40%, the desired effect cannot be obtained;
If the Mn content is exceeded, the toughness and weldability will deteriorate.
It was set at 0.40-1.00%. d) Cr The Cr component should be contained at 0.40% or more to ensure hardenability and strength, but if it is contained in excess of 1.20%, toughness will deteriorate, so the Cr content should be set at 0.40 to 1.20%. Established. e) Ni The Ni component has the effect of ensuring hardenability and improving low-temperature toughness, so it should be contained at 2.0% or more, but in consideration of economic efficiency, the upper limit was set at 4.2%. In addition, Ni is an element that can increase hardenability without reducing toughness, and
2.7 to produce 150mm thick HT100 steel plate
It is desirable to contain it in an amount of % or more. f) Mo Mo component increases the hardenability of steel,
It has the effect of increasing the tempering resistance and increasing its strength, but its content is 0.40
If the Mo content is less than 0.80%, the desired effect cannot be obtained, and if it exceeds 0.80%, the weldability will be significantly deteriorated.
It was set at 0.40-0.80%. g) V The V component has the effect of increasing strength through precipitation strengthening, and is contained at 0.01% or more to ensure the desired strength.
If the V content exceeds 0.06%, the toughness and weldability will deteriorate.
It was set at 0.01-0.06%. In addition, in the method of the present invention, the N content is kept low at 0.004% or less, and by performing low-temperature tempering, sufficient strength can be ensured with a small amount of V addition, so the V content is reduced to 0.01%. It is most desirable to adjust the content to ~0.04% in order to ensure toughness. h) B The B component can greatly improve the hardenability of steel by adding a small amount, so it should be included at 0.0004% or more, but if it is included in excess of 0.0015%, the toughness will deteriorate, so B
The content was set at 0.0004% to 0.0015%. In addition,
In the method of the present invention, the N content is reduced to 0.0040%.
The B content is kept low as below.
A range of 0.0004 to 0.0010% is desirable. i) Cu The Cu component has the effect of improving the strength, toughness, and corrosion resistance of steel, but if it is contained in excess of 0.50%, it may deteriorate hot workability, toughness, or hot cracking resistance during welding. Therefore, the Cu content was set at 0.50% or less. In addition,
Although the Cu content is small and its addition effect is recognized, in order to obtain a noticeable effect, 0.05
% or more of Cu is desirable. j) Sol.Al The Sol.Al component has the effect of deoxidizing the steel and increasing the hardenability improvement effect of the B component, but if its content is less than 0.010%, the desired effect is not obtained. On the other hand, if the Sol.Al content exceeds 0.100%, the toughness will deteriorate, so the Sol.Al content was set at 0.010 to 0.100%. k) P and S It is desirable to reduce these impurities as much as possible in order to improve the toughness of steel. Yield strength of steel by quenching and tempering:
In order to satisfy 90Kgf/mm 2 or more, tensile strength: 97Kgf/mm 2 or more, it is preferable to temper at a low temperature, but at this time, if the P content is higher than 0.008%, tempering will cause brittleness. Toughness will be significantly reduced. Therefore, the P content
It was set at 0.008% or less. Furthermore, if the S content increases beyond 0.003%, coarse MnS will be produced, which will be elongated during rolling and cause deterioration of toughness, so the S content was set at 0.003% or less. l) N Setting N to less than 0.0040% is an extremely effective means for increasing the hardenability of steel and improving the strength and toughness of the base metal. That is, the N content is 0.0040
% or less, and by adjusting the Sol.Al content to 0.01 to 0.10%, the amount of solid solution B can be reduced to 0.0003ppm.
As a result, the hardenability is improved. Furthermore, since the amount of N is low, coarsening of AlN is suppressed and toughness is improved. Furthermore,
Since the generation of VN is suppressed by lowering the N content, V is uniformly dissolved in solid solution at the normal austenitizing temperature, which also has the effect of limiting the amount of V added. For this reason, the N content was reduced to 0.0040%.
It was determined as follows. m) PcM (weld crack susceptibility index) Even if preheating is performed at a sufficiently high temperature during welding, the formula PcM (%) = C (%) + Si (%) / 30 + Mn (%) / 20 + Cu (%) / PcM (welding crack susceptibility index) expressed as 20 + Ni (%) / 60 + Cr (%) / 20 + Mo (%) / 15 + V (%) / 10 + 5 × B (%) is
If it exceeds 0.31%, the incidence of cold cracking becomes extremely high and sufficient weldability cannot be ensured, so PcM was set at 0.31% or less. B Heat treatment conditions a) Heating temperature before quenching The reason why the heating temperature before quenching is set to the Ac 3 transformation point or higher is to completely austenite the steel and uniformly dissolve the alloying elements as a solid solution.
Heating below the transformation point does not allow the alloying elements to form a uniform solid solution. On the other hand, the heating temperature
If the temperature exceeds 1000℃, the austenite crystal grains will become coarser and the toughness will decrease .
1000℃]. b) Tempering temperature The reason for tempering at a temperature of 560℃ or higher is to remove the strain introduced by quenching and to improve strength and toughness by finely precipitating carbides. If the temperature is lower than 0.degree. C., the above effects cannot be obtained. on the other hand,
If the tempering temperature exceeds 630℃, the strength of the steel material will decrease and the yield strength will no longer satisfy the requirements of 90Kgf/mm 2 or higher and tensile strength of 97Kgf/mm 2 or higher. It was set as ℃. Note that one of the characteristics of the method of the present invention is that the steel material is heated and held at the tempering temperature and then water-cooled, and such treatment can significantly improve the low-temperature toughness. This is because, for example, in steel materials with a wall thickness exceeding 40 mm, the cooling rate after tempering decreases and the susceptibility to tempering brittleness increases. If you ensure cooling rate: 0.5~6.0℃/sec,
This is because the above-mentioned disadvantages will be resolved. In addition, the method of this invention has plate thickness: 40 mm ~
It is particularly effective in manufacturing 150mm high-tensile, thick-walled steel plates. This is because for steel materials with a wall thickness of less than 40 mm, it is relatively easy to ensure the strength and toughness of the base material without adding large amounts of alloying elements. Also, if the plate thickness exceeds 150 mm, the water cooling effect will not be obtained. Next, the present invention will be explained using examples and comparing with comparative examples. Examples First, steels A to F and comparison steels G to I, which are subject to the present invention and have chemical compositions as shown in Table 1, were melted. Next, this was made into a 150 mm thick slab by hot forging, and then into a 100 mm thick steel plate by hot rolling. The rolling heating temperature at this time was 1150°C. Next, the obtained 100 mm thick steel plate was reheated to 920°C as shown in Table 2, water quenched, and then heated to 580°C or 600°C for 1
It was tempered by holding it for a period of time and then cooling it in water. Separately, steels A to F targeted by the present invention were quenched at 600°C in the same manner as above.
The conventional method involves heating and holding for one hour and then cooling in the air.
【表】
注2)*印は、本発明範囲から外れていることを示す
。
[Table] Note 2) * indicates that it is outside the scope of the present invention.
【表】
焼入れ・焼もどし処理をも行つた。
これらの各鋼板の板厚中央部から、JIS4号シヤ
ルピー試験片と、8.5φで平行部長さ:50mmの丸棒
引張試験片とをそれぞれ圧延方向に採取し、その
機械的性質を調査した。
これらの結果を第2表に併せて示した。
第2表からも明らかなように、本発明法1〜12
によれば、降伏点:90Kgf/mm2以上、引張強さ:97
Kgf/mm2以上を満足してHT100鋼材としての強度
を満たすとともに、衝撃破面遷移温度も−60℃以
下という優れた靭性を有する鋼板の得られること
がわかる。
これに対して、比較法13〜21によつて得られた
鋼板は、いずれも本発明法によつて得られた鋼板
に比して靭性が劣つていることがわかる。
更に、本発明法1〜12によつて得られた各鋼板
よりy開先拘束割れ試験片(板厚:50mm)を採取
し、125℃に予熱後、入熱量:17KJ/cmでMIG溶
接し、表面割れ、ルート割れ、断面割れの有無を
調査したところ、いずれも欠陥を発生せずという
良好な結果が得られた。
上述のように、この発明によれば、優れた靭性
と高強度とを兼備し、かつ溶接性も良好な厚肉高
張力鋼材を得ることができ、鋼構造物の性能をよ
り以上に向上することが可能となるなど、工業上
有用な効果がもたらされるのである。[Table] Hardening and tempering treatments were also performed. A JIS No. 4 Shapey test piece and a round bar tensile test piece with a diameter of 8.5 and a parallel length of 50 mm were taken from the center of the thickness of each of these steel plates in the rolling direction, and their mechanical properties were investigated. These results are also shown in Table 2. As is clear from Table 2, methods 1 to 12 of the present invention
According to, yield point: 90Kgf/mm 2 or more, tensile strength: 97
It can be seen that a steel plate can be obtained which satisfies Kgf/mm 2 or more and satisfies the strength as an HT100 steel material, and also has excellent toughness with an impact fracture transition temperature of -60°C or less. On the other hand, it can be seen that the steel plates obtained by Comparative Methods 13 to 21 are all inferior in toughness to the steel plates obtained by the method of the present invention. Furthermore, y groove restrained crack test pieces (plate thickness: 50 mm) were taken from each steel plate obtained by methods 1 to 12 of the present invention, and after preheating to 125°C, MIG welding was performed at a heat input of 17 KJ/cm. When we investigated the presence or absence of surface cracks, root cracks, and cross-sectional cracks, good results were obtained, with no defects occurring in any of them. As described above, according to the present invention, it is possible to obtain a thick high-strength steel material that has both excellent toughness and high strength and also has good weldability, thereby further improving the performance of steel structures. This brings about industrially useful effects, such as making it possible to
Claims (1)
0.31%以下である成分組成範囲を有し、板厚:40
mm〜150mmの鋼板を、〔Ac3変態点〜1000℃〕の温
度域に加熱後、焼入れし、次いで560〜630℃に加
熱後水冷するという焼もどし処理を施すことを特
徴とする、溶接性の良好な引張強さが97Kgf/mm2以
上の高強度高靭性鋼材の製造方法。[Claims] 1. In weight percentage: C: 0.07-0.15%, Si: 0.15% or less, Mn: 0.40-1.00%, Cr: 0.40-1.20%, Ni: 2.0-4.2%, Mo: 0.40-0.80 %, V: 0.01-0.06%, B: 0.0004-0.0015%, Cu: 0.50% or less, sol.Al: 0.010-0.100%, P: 0.008% or less, S: 0.003% or less, N: 0.0040% or less, Fe and other unavoidable impurities: the remainder, and the weld cracking susceptibility index (PcM) is
It has a component composition range of 0.31% or less, plate thickness: 40
Weldability, characterized by subjecting a steel plate of mm to 150 mm to a tempering treatment in which it is heated to a temperature range of [Ac 3 transformation point to 1000 °C], quenched, then heated to 560 to 630 °C, and then water-cooled. A method for manufacturing high-strength, high-toughness steel materials with a good tensile strength of 97 Kgf/mm 2 or more.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17770183A JPS6070120A (en) | 1983-09-26 | 1983-09-26 | Manufacture of steel material with high strength, toughness and satisfactory weldability |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP17770183A JPS6070120A (en) | 1983-09-26 | 1983-09-26 | Manufacture of steel material with high strength, toughness and satisfactory weldability |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS6070120A JPS6070120A (en) | 1985-04-20 |
| JPH0120210B2 true JPH0120210B2 (en) | 1989-04-14 |
Family
ID=16035588
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP17770183A Granted JPS6070120A (en) | 1983-09-26 | 1983-09-26 | Manufacture of steel material with high strength, toughness and satisfactory weldability |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS6070120A (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62174321A (en) * | 1986-01-24 | 1987-07-31 | Kobe Steel Ltd | Manufacture of 80kgf/mm2 secondary grade steel plate having good toughness of base metal and welded joint part |
| US7967923B2 (en) | 2008-10-01 | 2011-06-28 | Nippon Steel Corporation | Steel plate that exhibits excellent low-temperature toughness in a base material and weld heat-affected zone and has small strength anisotropy, and manufacturing method thereof |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5782459A (en) * | 1980-11-10 | 1982-05-22 | Nippon Steel Corp | Steel products with superior weldability |
| JPS604250B2 (en) * | 1981-06-22 | 1985-02-02 | 新日本製鐵株式会社 | Manufacturing method of high toughness heat-treated high tensile strength steel |
-
1983
- 1983-09-26 JP JP17770183A patent/JPS6070120A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS6070120A (en) | 1985-04-20 |
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