JPS621456B2 - - Google Patents
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- JPS621456B2 JPS621456B2 JP15679682A JP15679682A JPS621456B2 JP S621456 B2 JPS621456 B2 JP S621456B2 JP 15679682 A JP15679682 A JP 15679682A JP 15679682 A JP15679682 A JP 15679682A JP S621456 B2 JPS621456 B2 JP S621456B2
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- less
- brittle fracture
- steel
- points
- toughness
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Classifications
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
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- 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 Articles (AREA)
Description
本発明は母材においては脆性破壊伝播停止特性
にすぐれ、また溶接部においては脆性破壊発生特
性のすぐれた高張力鋼の製造法にかかわるもので
ある。
LPG、LNG等のエネルギー源を貯蔵する低温
容器用鋼材や寒冷地で使用に供せられるラインパ
イプ用鋼材には、その構造物としての安全性を確
保するために脆性破壊伝播停止特性に関する高い
靭性値が必要とされている。鋼材の使用される環
境が厳しくなるにつれて、より高い靭性値が必要
となる傾向は今後ますます強くなるであろう。こ
のような趨勢に対処するために、鋼に合金元素、
特にNiを添加したり、また熱間圧延方法あるい
は熱処理方法に工夫をこらしているのが実状であ
る。
ところで一般に鋼構造物、とりわけ大型鋼構造
物では主要部材は主として溶接によつて製作さ
れ、これらの構造物で脆性破壊の発生のおそれが
あるとすれば、それは殆んどの場合溶接部であ
り、したがつて高い溶接部靭性(脆性破壊発生に
対する抵抗)を鋼材に付与ることは重要である。
大型鋼構造物の安全性、すなわち脆性破壊による
崩壊の防止を意図するならば、溶接部においては
主として脆性破壊発生に対する抵抗、すなわち溶
接部靭性にすぐれ、また母材においては一たび発
生した脆性亀裂の伝播を阻止する性能、すなわ
ち、脆性破壊伝播停止特性にすぐれた鋼材を使用
に供することが肝要である。しかしながら、従来
技術においては両特性を高い水準で具備し、かつ
大量使用を可能ならしめる程度の製造コストで製
造するには困難が大きかつた。たとえばNi添加
によつて脆性破壊伝播停止特性を向上させ得るも
のの、Ni添加量の増加と共に溶接部の最高硬さ
は高くなり、溶接部の靭性、特に脆性破壊発生の
指標である限界CODが低下することが知られて
いる(鉄と鋼、68(1982)S629、図2)。
かかる実状を踏えて本発明者らは、鋼材の脆性
破壊伝播現象について従来の常識とは全く異なる
現象を発見し、詳細な冶金的検討を加えることに
よつて溶接部においてはCOD値によつて特徴付
けられる脆性破壊発生特性、母材においては脆性
破壊伝播停止特性の優れた高張力鋼の製造法を発
明するに到つたものである。
以下に本発明の詳細を記述するが初めに成分限
定の理由を述べる。
Cは鋼材の所要強度を確保するためには不可欠
な元素であつて、0.05%未満では強度不足となる
惧れがあり、かつ本発明の最も特徴とする微細分
散したマルテンサイトの量が過少となり、また
0.15%を越えると、溶接部靭性が低下するので添
加量を0.05%以上0.15%以下に限定した。
Siは溶鋼中の脱酸を促進し、しかも固溶体強化
による強度上昇の効果を期待できる元素であるの
で0.01%以上添加するが、溶接部にしばしば高炭
素マルテンサイトを発生させ、溶接部靭性を劣化
させる傾向が大きいので0.3%を上限とした。
Mnは母材の低温靭性を改善させる元素として
有効であるので下限は0.5%としたが、過量に添
加すると溶接部の硬度を上昇させ冷間割れ性を増
大させ、また溶接部靭性の低下も招来するので、
この発明では2.0%を上限にした。
Alは良く知られているように強力な脱酸剤で
あり、また結晶粒の微細化にも効果的に機能する
ので、基本成分の一種として不可欠な元素である
が、過量に添加すると材質に有害であるアルミナ
クラスターを形成するため上限として0.1%を設
定した。
本発明においては適量のTiおよびNの添加は
必須である。TiおよびNは鋼材中でTiN化合物を
形成し、適当に分散したTiN析出物はオーステナ
イト結晶粒の粗大化抑制の機能を有するからであ
る。添加Ti量が0.005%未満ではこの効果を期待
しにくく、また0.030%を超過すると、オーステ
ナイト結晶粒粗大化防止に無効であるのみなら
ず、材質、特に溶接部靭性に有害であるような粗
大なTiN化合物生成の傾向が顕著になるので、
0.030%を上限とした。
添加する趣旨から明らかなようにNはTiNを形
成するに必要かつ十分な量に制御することが必要
であるが製鋼作業におけるバラツキも考慮して添
加範囲を(0.2〜0.5)×Ti%とした。
Vは通常は析出強化元素として活用されるが、
本発明の趣旨ではむしろ焼入性向上の観点から必
要であれば添加する。過量添加は、母材の脆性破
壊伝播停止特性および溶接部靭性を劣化するので
0.2%以下に制限した。
Nbは熱間圧延時のオーステナイト結晶粒の微
細化に有効であるが、溶接熱影響部を硬化させ結
果的には靭性劣化を惹起するので、0.08%以下の
添加量に制限した。
Cr、Moはいずれも焼入性および母材の強化の
観点では適当量の使用は有効であるが、焼入性向
上機能はまた溶接部を著しく硬化させるので、
Crについては1.0%、Moについては0.5%をその
上限とした。
Niは母材の脆性破壊伝播停止特性を著しく向
上させる元素として知られているが、前記したよ
うに、溶接部の硬度上昇をもたらし、溶接部靭性
を低下させること、および本発明の趣旨から添加
する場合であつても高々1.5%とした。
Cuは固溶体強化元素として必要とあれば添加
することが可能であるが過量添加は母材、溶接部
靭性の劣化、また熱間脆性の誘発の恐れがあり
0.5%以下に制限した。
以上の各元素の個々の添加量の他に本発明にお
いては{C+Mn/6+Cr+Mo+V/5+Ni+C
u/15}(以
後、本発明では炭素当量と呼ぶ)の値が0.40%以
下にあることを必須条件としている。炭素当量が
0.40%を超えると、溶接部の硬度、特に溶接入熱
が比較的小さい場合の硬度が著しく高くなり、溶
接部靭性、とりわけ脆性破壊発生特性の指標であ
る限界COD値の低下がより顕著になるので上限
値として0.40%を設定した。
次に製造条件の限定理由について記述する。
熱間圧延前に鋳片または鋼片をAr3点以上に加
熱するのは鋳片または鋼片を全体に一様にオース
テナイト化するためであつて、圧延後に所要の機
械的特性値を得るには不可欠である。加熱温度を
1150℃以下に制限することによつて、必須元素と
して添加されているTiおよびNの効能と相まつ
て圧延前のオーステナイト結晶粒を細粒にかつ整
粒に保つことが可能であるとの理由により加熱温
度に上限を設定した。特に、優れた脆性破壊停止
特性を得るには、整粒のオーステナイト結晶粒を
得ることは必要条件である。本発明に該当する鋼
材の化学成分は低炭素当量であつてこれはAr3変
態点が相対的に高いことを意味する。したがつ
て、圧延終了後のオーステナイト結晶粒の細粒化
を計るために900℃以下での圧下量を30%以上確
保することを必須条件とする。ただし900℃以下
での圧延を過度に行うと集合組織が発達し、セパ
レーシヨンと称する板面平行な割れが発生し易く
なるので、圧下量の上限を80%に制限した。セパ
レーシヨンの導入により見掛けの脆性破壊特性の
向上が得られるが、板厚方向に応力負荷がかかる
場合の安全性確保を考慮すれば、むしろセパレー
シヨンの発生は抑制すべきである。また圧延仕上
温度はAr3変態点以上とし、初析フエライトの析
出を抑制しなければならない。
鋼の含有成分量を上記の範囲に制御し、かつ炭
素当量を0.40%以下に制限することにより、当該
鋼をAc3点以上1150℃以下に加熱した後、Ar3点
以上で熱間圧延を施し、圧延後空気中に放冷する
ことによつて得られる主たる金属組織は厚板材相
当の鋼材厚みの場合にはフエライトとパーライト
の混合組織が主体である。しかるに本発明におい
てはAr3点以上で熱間圧延した後、Ar3点以上の
温度から35℃/秒以上90℃/秒以下の冷却速度
(750℃から200℃の間の平均冷却速度を意味す
る。)で強制的に冷却し、主たる組織をフエライ
トと微細に分散したマルテンサイトの混合組織に
し、かつフエライト中には微細な析出物の析出を
可能な限り抑制することを特徴とするものであ
る。
本発明の成分範囲では35℃/秒未満の冷却速度
では、第二相としてのマルテンサイトを得ること
ができず、90℃/秒超の冷却速度ではフエライト
の析出が抑制され、本発明の最も特徴とするフエ
ライトと微細分散したマルテンサイトの混合組織
を確保することが困難となるので、上記範囲に限
定した。
本発明者らは鋼材の脆性破壊伝播停止特性を支
配する冶金因子として、従来から知られている結
晶粒の微細化とNiの添加の他に、微細析出物の
少ないフエライトと微細分散したマルテンサイト
の混合組織を生成させることによつて脆性破面生
成表面エネルギーの増加をはかることができるこ
とを発見したものであり、この事実は本発明の根
幹をなすものである。脆性破壊を停止させるに
は、進展する脆性亀裂の有する運動エネルギーを
吸収する必要があるが、本発明者は詳細な実験と
観察を基にして、既存技術の他にさらに2種の方
策によつて、脆性破面生成表面エネルギーの増加
が可能であることを見出した。即ち、その第一の
要点は脆性破面がフエライト結晶粒を越えて隣接
する結晶粒に伝播する際結晶粒界にはテイアリツ
ジと呼ばれる延性破壊部分が形成されるが、その
テイアリツジの塑性変形能を上昇させる方法であ
る。そのためには塑性変形能の大きい、フエライ
ト結晶粒を確保する必要がある。その最も効果的
な方法が圧延後の急冷である。圧延後の冷却速度
が空冷程度の場合には粒内に無数の炭化物等が析
出し、あるいは集合体を形成する結果、フエライ
ト結晶粒の塑性変形能は著しく低下する。
第2の要点はフエライトと微細分散したマルテ
ンサイトによつて高い加工硬化係数を得ることが
でき、このことは塑性変形の局在下を抑制し、こ
れはテイアリツジの塑性変形能を増加させる効果
を有し結果的には、脆性破面生成エネルギーの増
加に寄与するものである。第1点および第2点の
技術思想は相互に独立したものであるが本発明の
製造法に従えば両方の効果を同時に活用でき、脆
性破壊伝播停止特性の大幅な向上が可能なのであ
る。
従来技術においては、微細分散したマルテンサ
イトは広義の意味で靭性に悪影響を与えると考え
られてきたが、本発明においては、その悪影響が
でない理由を説明する。靭性に対する、微細分散
したマルテンサイトの悪影響は主として従来は溶
接部において知られた現象であり、その解析が行
なわれてきた。オーステナイト温度域から急速に
冷却する場合、主として含有する化学成分によつ
て決まるマルテンサイト変態開始温度以下でマル
テンサイトが形成されるが、生成したマルテンサ
イトは体積膨張を伴なうために隣接したフエライ
トに転位が導入される。この事実は透過型電子顕
微鏡観察によつて本発明者は確認している。しか
るにこのような転位が導入された後もさらに急速
に冷却を続けることにより鋼中に固溶する炭素あ
るいは窒素等が導入された転位に拡散し、固着す
る確率は小さくなる。従つて室温以下にまで急冷
を続けた場合には微細分散したマルテンサイトが
形成されるもののそれに隣接している塑性変形能
に富んだフエライト粒内に自由な転位が随伴して
いることが特徴である。この事はたとえ微細分散
したマルテンサイトが脆く、外力によつて破壊し
たとしても隣接する自由転位の移動によつて、そ
れが脆性破壊発生の源となるグリフイス亀裂とし
て働らきにくいことを意味している。事実、同一
成分の鋼材を、本発明に従つて製造した場合と圧
延後に空冷した場合(組織はフエライト・パーラ
イト鋼)とにおける、脆性破壊発生特性は殆んど
優劣の差はない。COD値についてはむしろ本発
明法になる鋼材の方がやや優れてさえいる。この
結果を第1図に示す。他方、溶接部に生成される
微細なマルテンサイトはマルテンサイト変態後も
徐冷されることおよびマルテンサイトに隣接する
金属組織が多くの場合靭性の低い、上部ベーナイ
トであつて、脆弱なマルテンサイトがグリフイス
亀裂として作用する可能性が大きく、結果として
シヤルピー試験あるいはCOD試験等で評価され
る靭性値を低下させるものと考えられる。
以上詳細に述べてきた本発明の技術思想に基ず
き製造した鋼材の母材の脆性破壊伝播停止特性お
よび溶接部をシミユレートした溶接再現熱サイク
ルを施した場合の脆性破壊発生特性を従来法との
比較において第1表に示す。同表で冷却速度は鋼
板の板厚中心部に装着した熱電対で測定した750
℃乃至200℃の間の平均冷却速度を意味する。脆
性破壊伝播停止特性は簡易型のDWTT(Drop
Weight Tear Test)を使用し、試験片破面が脆
性破面率50%を示す温度をその指標とした。試験
片形状は厚み14mm、長さ180mm、幅45mmであり、
深さ5mmのノツチ部は脆性破壊発生を容易にし、
かつ逆破面を防止するため、局所的に脆化させて
いる。溶接部における脆性破壊発生特性は
BS5762に準拠したCOD試験によつて評価した。
また溶接再現熱サイクルを施した鋼材のブイツカ
ーズ硬度を荷重20Kgで測定した。
第1表から明らかなように、本発明による鋼材
は2%Ni含有鋼とほぼ同等の脆性破壊伝播停止
特性を有し、溶接部についてはその硬度は低く、
また溶接部靭性の指標である限界CODは、はる
かに優れていることが明らかである。溶接部の硬
度が低いことは溶接冷間割れあるいは溶接部の応
力硫化物腐食割れ特性にも優れていると言えよ
う。
The present invention relates to a method for manufacturing high-strength steel that has excellent brittle fracture propagation arresting properties in the base material and excellent brittle fracture occurrence properties in the welded part. Steel materials for low-temperature containers that store energy sources such as LPG and LNG, and steel materials for line pipes used in cold regions, have high toughness to ensure the safety of their structures. value is required. As the environment in which steel materials are used becomes more severe, the tendency for higher toughness values to be required will become stronger in the future. To cope with this trend, alloying elements,
In particular, the current situation is that Ni is added, and the hot rolling method or heat treatment method is devised. By the way, in general steel structures, especially large steel structures, the main components are mainly manufactured by welding, and if there is a risk of brittle fracture occurring in these structures, it is almost always the welded parts. Therefore, it is important to provide steel with high weld toughness (resistance to brittle fracture occurrence).
If the aim is to ensure the safety of large steel structures, that is, to prevent collapse due to brittle fracture, the welds should mainly have resistance to brittle fractures, that is, excellent weld toughness, and the prevention of brittle cracks once generated in the base metal. It is important to use steel materials that have excellent properties to stop the propagation of brittle fractures, that is, to stop the propagation of brittle fractures. However, in the prior art, it is very difficult to manufacture a device that has both characteristics at a high level and at a manufacturing cost that allows mass use. For example, although the addition of Ni can improve brittle fracture propagation arresting properties, as the amount of Ni added increases, the maximum hardness of the weld increases, and the toughness of the weld, especially the limit COD, which is an indicator of brittle fracture occurrence, decreases. (Tetsu to Hagane, 68 (1982) S629, Figure 2). Based on these actual circumstances, the present inventors discovered a phenomenon that is completely different from the conventional wisdom regarding the brittle fracture propagation phenomenon of steel materials, and by adding detailed metallurgical studies, it was found that the COD value of the welded part This led to the invention of a method for manufacturing high-strength steel that is characterized by excellent brittle fracture occurrence characteristics and, in the base material, excellent brittle fracture propagation arresting characteristics. The details of the present invention will be described below, but first the reason for limiting the ingredients will be described. C is an essential element to ensure the required strength of steel materials, and if it is less than 0.05%, there is a risk that the strength will be insufficient, and the amount of finely dispersed martensite, which is the most characteristic of the present invention, will be too small. ,Also
If it exceeds 0.15%, the toughness of the weld zone will deteriorate, so the amount added is limited to 0.05% or more and 0.15% or less. Si is an element that promotes deoxidation in molten steel and can be expected to increase strength through solid solution strengthening, so it is added in an amount of 0.01% or more, but it often generates high-carbon martensite in welds and deteriorates weld toughness. The upper limit was set at 0.3%, as there is a large tendency to Mn is effective as an element for improving the low-temperature toughness of the base metal, so the lower limit was set at 0.5%; however, if added in excess, it increases the hardness of the weld, increases the cold cracking resistance, and also reduces the toughness of the weld. Because I'm inviting you,
In this invention, the upper limit is set at 2.0%. As is well known, Al is a strong deoxidizing agent and also functions effectively in refining crystal grains, so it is an essential element as a basic component. The upper limit was set at 0.1% because it forms harmful alumina clusters. In the present invention, addition of appropriate amounts of Ti and N is essential. This is because Ti and N form a TiN compound in the steel material, and appropriately dispersed TiN precipitates have the function of suppressing coarsening of austenite crystal grains. If the amount of added Ti is less than 0.005%, it is difficult to expect this effect, and if it exceeds 0.030%, it is not only ineffective in preventing austenite crystal grain coarsening, but also causes coarse grains that are harmful to the material, especially the weld toughness. Since the tendency of TiN compound formation becomes noticeable,
The upper limit was set at 0.030%. As is clear from the purpose of adding N, it is necessary to control the amount of N to a necessary and sufficient amount to form TiN, but taking into account the variations in steelmaking operations, the addition range was set as (0.2 to 0.5) x Ti%. . V is usually utilized as a precipitation strengthening element, but
Rather, in the spirit of the present invention, it is added if necessary from the viewpoint of improving hardenability. Excessive addition will deteriorate the brittle fracture propagation arresting properties of the base metal and the weld toughness.
It was limited to 0.2% or less. Although Nb is effective in refining austenite grains during hot rolling, it hardens the weld heat affected zone and ultimately causes deterioration of toughness, so the amount added was limited to 0.08% or less. Although it is effective to use appropriate amounts of both Cr and Mo from the viewpoint of hardenability and strengthening of the base metal, the hardenability improving function also significantly hardens the welded part, so
The upper limit was set at 1.0% for Cr and 0.5% for Mo. Ni is known as an element that significantly improves the brittle fracture propagation arresting properties of the base metal, but as mentioned above, it increases the hardness of the weld and reduces the toughness of the weld, and is added for the purposes of the present invention. Even if it does, it is set at 1.5% at most. Cu can be added as a solid solution strengthening element if necessary, but adding too much may cause deterioration of the toughness of the base metal and weld zone, as well as induction of hot embrittlement.
It was limited to 0.5% or less. In addition to the individual addition amounts of each element mentioned above, in the present invention, {C+Mn/6+Cr+Mo+V/5+Ni+C
u/15} (hereinafter referred to as carbon equivalent in the present invention) is an essential condition that the value is 0.40% or less. Carbon equivalent is
If it exceeds 0.40%, the hardness of the weld, especially when the welding heat input is relatively small, will increase significantly, and the weld toughness, especially the critical COD value, which is an indicator of brittle fracture occurrence characteristics, will decrease more significantly. Therefore, we set 0.40% as the upper limit. Next, the reasons for limiting the manufacturing conditions will be described. The purpose of heating a slab or steel slab to Ar 3 or higher before hot rolling is to uniformly austenite the entire slab or steel slab, and to obtain the required mechanical property values after rolling. is essential. heating temperature
The reason is that by limiting the temperature to 1150℃ or less, it is possible to keep the austenite crystal grains fine and well-sized before rolling, together with the effectiveness of Ti and N added as essential elements. An upper limit was set on the heating temperature. In particular, in order to obtain excellent brittle fracture arresting properties, it is a necessary condition to obtain well-sized austenite crystal grains. The chemical composition of the steel material applicable to the present invention has a low carbon equivalent, which means that the Ar 3 transformation point is relatively high. Therefore, in order to refine the austenite crystal grains after rolling, it is essential to ensure a rolling reduction of 30% or more at 900°C or lower. However, excessive rolling at temperatures below 900°C will cause the texture to develop and cracks parallel to the sheet surface, called separation, will likely occur, so the upper limit of the rolling reduction was limited to 80%. Although the apparent brittle fracture properties can be improved by introducing separation, in consideration of ensuring safety when stress is applied in the thickness direction, the occurrence of separation should be suppressed. In addition, the finishing temperature of rolling must be at least the Ar 3 transformation point to suppress the precipitation of pro-eutectoid ferrite. By controlling the content of the steel components within the above range and limiting the carbon equivalent to 0.40% or less, the steel can be heated to 3 or more Ac points and 1150℃ or less, and then hot rolled at 3 or more Ar points. The main metallographic structure obtained by cooling in the air after rolling is mainly a mixed structure of ferrite and pearlite in the case of a steel material whose thickness is equivalent to that of a thick plate. However, in the present invention, after hot rolling at 3 or more Ar points, the cooling rate from the temperature at 3 or more Ar points is 35°C/sec to 90°C/sec (meaning the average cooling rate between 750°C and 200°C). ), the main structure is a mixed structure of ferrite and finely dispersed martensite, and the precipitation of fine precipitates in the ferrite is suppressed as much as possible. be. In the composition range of the present invention, martensite as a second phase cannot be obtained at a cooling rate of less than 35°C/sec, and precipitation of ferrite is suppressed at a cooling rate of more than 90°C/sec. Since it would be difficult to secure the characteristic mixed structure of ferrite and finely dispersed martensite, it was limited to the above range. In addition to grain refinement and the addition of Ni, which are conventionally known as metallurgical factors that control the brittle fracture propagation arresting characteristics of steel materials, the present inventors have investigated ferrite with few fine precipitates and finely dispersed martensite. It has been discovered that the surface energy for forming a brittle fracture surface can be increased by generating a mixed structure of , and this fact forms the basis of the present invention. In order to stop brittle fracture, it is necessary to absorb the kinetic energy of the propagating brittle crack, but based on detailed experiments and observations, the present inventor has devised two additional measures in addition to the existing technology. We found that it is possible to increase the surface energy for forming brittle fracture surfaces. That is, the first point is that when a brittle fracture surface propagates across a ferrite grain to an adjacent grain, a ductile fracture portion called a tear ridge is formed at the grain boundary, but the plastic deformation ability of the tear ridge is This is a method of increasing For this purpose, it is necessary to secure ferrite crystal grains with large plastic deformability. The most effective method is rapid cooling after rolling. When the cooling rate after rolling is about that of air cooling, numerous carbides and the like precipitate within the grains or form aggregates, resulting in a marked decrease in the plastic deformability of the ferrite crystal grains. The second point is that a high work hardening coefficient can be obtained by ferrite and finely dispersed martensite, which suppresses the localization of plastic deformation, which has the effect of increasing the plastic deformation ability of the tie ridge. As a result, this contributes to an increase in the energy for forming brittle fracture surfaces. Although the technical ideas of the first point and the second point are independent from each other, if the manufacturing method of the present invention is followed, both effects can be utilized at the same time, and the brittle fracture propagation stopping characteristics can be significantly improved. In the prior art, it has been thought that finely dispersed martensite has an adverse effect on toughness in a broad sense, but in the present invention, the reason why it does not have such an adverse effect will be explained. The adverse effect of finely dispersed martensite on toughness is a phenomenon known mainly in welds and has been analyzed. When rapidly cooling from the austenite temperature range, martensite is formed below the martensite transformation start temperature, which is determined mainly by the chemical components contained, but the formed martensite is accompanied by volume expansion, so the adjacent ferrite A dislocation is introduced. This fact has been confirmed by the present inventor through transmission electron microscopy. However, by continuing to rapidly cool the steel even after such dislocations have been introduced, carbon, nitrogen, etc. dissolved in the steel will diffuse into the introduced dislocations, reducing the probability that they will stick. Therefore, when rapid cooling is continued to below room temperature, finely dispersed martensite is formed, but it is characterized by the accompanying free dislocations within the adjacent ferrite grains, which are rich in plastic deformability. be. This means that even if finely dispersed martensite is brittle and fractured by an external force, it is unlikely to act as a Griffith crack, which is the source of brittle fracture, due to the movement of adjacent free dislocations. There is. In fact, there is almost no difference in the brittle fracture occurrence characteristics when steel materials with the same composition are manufactured according to the present invention and when they are air-cooled after rolling (ferrite/pearlite steel structure). In terms of COD value, the steel produced using the method of the present invention is even slightly better. The results are shown in FIG. On the other hand, the fine martensite generated in the weld zone is slowly cooled even after the martensite transformation, and the metal structure adjacent to the martensite is often upper bainite with low toughness, and the brittle martensite is There is a high possibility that this will act as a Griffiths crack, and as a result, it is thought that the toughness value evaluated by the Shapey test or COD test will be reduced. The brittle fracture propagation arresting characteristics of the base metal of steel manufactured based on the technical idea of the present invention described in detail above and the brittle fracture occurrence characteristics when subjected to a welding reproduction thermal cycle simulating a welded part were compared with conventional methods. A comparison is shown in Table 1. In the same table, the cooling rate was measured with a thermocouple attached to the center of the thickness of the steel plate.
Means the average cooling rate between ℃ and 200℃. The brittle fracture propagation arresting property is a simple type of DWTT (Drop
Weight Tear Test) was used, and the temperature at which the fracture surface of the test piece showed a brittle fracture ratio of 50% was used as an index. The specimen shape is 14 mm thick, 180 mm long, and 45 mm wide.
The 5mm deep notch facilitates brittle fracture,
In addition, in order to prevent reverse fracture surfaces, they are locally embrittled. The characteristics of brittle fracture occurrence in welds are
Evaluated by COD test in accordance with BS5762.
In addition, the Buitskars hardness of the steel material subjected to the welding simulated thermal cycle was measured under a load of 20 kg. As is clear from Table 1, the steel material according to the present invention has almost the same brittle fracture propagation arresting properties as steel containing 2% Ni, and the hardness of the welded part is low.
It is also clear that the critical COD, which is an indicator of weld toughness, is much better. It can be said that the low hardness of the welded part also has excellent properties against weld cold cracking and stress sulfide corrosion cracking of the welded part.
【表】【table】
【表】【table】
【表】
なお本発明は主として脆性破壊伝播停止特性に
ついて記述してきたが、母材の延性値が大きいこ
とは主としてガスラインパイプで問題となる不安
定延性破壊の抑制にも有効に機能にするものであ
る。不安定延性破壊とDWTTでの吸収エネルギ
ーには相関のあることが知られているが、本発明
法による鋼材の方が従来法によるそれより高い吸
収エネルギーを示しているからである。
本発明においては溶接部については脆性破壊発
生特性を主たる対象にしているが溶接法あるいは
その後の熱処理に工夫をこらして溶接部における
脆性破壊伝播停止特性の向上に本発明の技術思想
を活用することも可能である。
以上記述した事実は主として鋼板についてであ
つてが、本発明の要件を満足していれば、鋼材の
形状、寸法については何等制約を与えるものでは
ない。[Table] Although the present invention has mainly been described regarding brittle fracture propagation arresting characteristics, the large ductility value of the base material makes it effective in suppressing unstable ductile fractures, which are a problem mainly in gas line pipes. It is. It is known that there is a correlation between unstable ductile fracture and absorbed energy in DWTT, but the steel produced by the method of the present invention exhibits higher absorbed energy than that produced by the conventional method. In the present invention, the main target is the brittle fracture occurrence characteristics of welded parts, but the technical idea of the present invention can be utilized to improve the brittle fracture propagation stopping characteristics in welded parts by devising the welding method or subsequent heat treatment. is also possible. Although the facts described above mainly concern steel plates, they do not impose any restrictions on the shape and dimensions of the steel material as long as the requirements of the present invention are satisfied.
第1図は本発明による鋼材の脆性破壊発生を従
来法によつて製造した鋼材のそれと比較した図で
ある。図において○印はvTrs(シヤルピー試験
における50%破面遷移温度)、●印はTδ0.2
(COD試験において限界CODが0.2mmを示す遷移
温度。COD試験はBS5762に準拠)である。
FIG. 1 is a diagram comparing the occurrence of brittle fracture in a steel material according to the present invention with that in a steel material produced by a conventional method. In the figure, the ○ mark is vTrs (50% fracture surface transition temperature in the Charpy test), and the ● mark is Tδ 0.2
(The transition temperature at which the limit COD is 0.2 mm in the COD test. The COD test complies with BS5762).
Claims (1)
%、Mn:0.5〜2.0%、Al:0.01〜0.1%、Ti:
0.005〜0.030%、N:(0.2〜0.5)×Ti%を含有
し、残部Feおよび不純物から成る鋼鋳片または
鋼片をAc3点以上1150℃以下に加熱した後、900
℃以下Ar3点以上の温度域における圧下率が30%
以上80%以下となる熱間圧延を施した後、Ar3点
以上から35℃/秒以上90℃/秒以下の冷却速度で
200℃以下まで冷却することを特徴とする溶接部
靭性および脆性破壊伝播停止特性の優れた高張力
鋼の製造法。 2 重量%でC:0.05〜0.15%、Si:0.01〜0.3
%、Mn:0.5〜2.0%、Al:0.01〜0.1%、Ti:
0.005〜0.030%、N:(0.2〜0.5)×Ti%を含有
し、さらにV:0.2%以下、Nb:0.08%以下、
Cr:1.0%以下、Mo:0.5%以下、Cu:0.5%以
下、Ni:1.5%以下の一種または二種以上を {C+Mn/6+Cr+Mo+V/5+Ni+Cu/1
5}≦0.40% となるように含有し、残部Feおよび不純物から
なる鋼鋳片または鋼片をAc3点以上1150℃以下に
加熱した後、900℃以下Ar3点以上の温度域にお
ける圧下率が30%以上80%以下となる熱間圧延を
施した後、Ar3点以上から35℃/秒以上90℃/秒
以下の冷却速度で200℃以下まで冷却することを
特徴とする溶接部靭性および脆性破壊伝播停止特
性の優れた高張力鋼の製造法。[Claims] 1 C: 0.05 to 0.15%, Si: 0.01 to 0.3 by weight
%, Mn: 0.5~2.0%, Al: 0.01~0.1%, Ti:
After heating a steel slab or billet containing 0.005 to 0.030%, N: (0.2 to 0.5) x Ti%, and the balance consisting of Fe and impurities to 1150℃ or less at 3 Ac points, 900
The reduction rate is 30% in the temperature range of 3 or more Ar points below ℃
After hot rolling to a temperature of 80% or more, the cooling rate is 35°C/sec or more and 90°C/sec or less from Ar 3 or more points.
A method for producing high-strength steel with excellent weld toughness and brittle fracture propagation arresting properties, which is characterized by cooling to below 200℃. 2 C: 0.05-0.15%, Si: 0.01-0.3 in weight%
%, Mn: 0.5~2.0%, Al: 0.01~0.1%, Ti:
Contains 0.005 to 0.030%, N: (0.2 to 0.5) x Ti%, further V: 0.2% or less, Nb: 0.08% or less,
One or more of Cr: 1.0% or less, Mo: 0.5% or less, Cu: 0.5% or less, Ni: 1.5% or less {C+Mn/6+Cr+Mo+V/5+Ni+Cu/1
5}≦0.40%, with the remainder being Fe and impurities, after heating the steel slab or billet to Ac 3 points or more and 1150°C or less, the reduction rate in the temperature range of Ar 3 points or more of 900°C or less Weld toughness characterized by hot rolling where the temperature is 30% or more and 80% or less, and then cooling from 3 Ar points or more to 200°C or less at a cooling rate of 35°C/sec or more and 90°C/sec or less. and a method for manufacturing high-strength steel with excellent brittle fracture propagation arresting properties.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15679682A JPS5947323A (en) | 1982-09-10 | 1982-09-10 | Production of high tension steel having excellent toughness in weld zone and property for stopping propagation of brittle fracture |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15679682A JPS5947323A (en) | 1982-09-10 | 1982-09-10 | Production of high tension steel having excellent toughness in weld zone and property for stopping propagation of brittle fracture |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5947323A JPS5947323A (en) | 1984-03-17 |
| JPS621456B2 true JPS621456B2 (en) | 1987-01-13 |
Family
ID=15635495
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15679682A Granted JPS5947323A (en) | 1982-09-10 | 1982-09-10 | Production of high tension steel having excellent toughness in weld zone and property for stopping propagation of brittle fracture |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5947323A (en) |
Families Citing this family (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6425916A (en) * | 1987-07-21 | 1989-01-27 | Nippon Steel Corp | Manufacture of high-strength steel for electric resistance welded tube excellent in toughness at low temperature |
| JPH02217416A (en) * | 1988-11-08 | 1990-08-30 | Nippon Steel Corp | Production of steel stock excellent in arresting property |
| JP4677685B2 (en) * | 2001-06-13 | 2011-04-27 | Jfeスチール株式会社 | Cooling method for thick-walled high-tensile hot-rolled steel strip |
| WO2005080621A1 (en) | 2004-02-19 | 2005-09-01 | Nippon Steel Corporation | Steel sheet or steel pipe being reduced in expression of baushinger effect, and method for production thereof |
| JP4058097B2 (en) | 2006-04-13 | 2008-03-05 | 新日本製鐵株式会社 | High strength steel plate with excellent arrestability |
| KR20090078807A (en) * | 2006-10-06 | 2009-07-20 | 엑손모빌 업스트림 리서치 캄파니 | Low yield ratio composite tissue steel line pipe with excellent strain aging resistance |
| JP4309946B2 (en) | 2007-03-05 | 2009-08-05 | 新日本製鐵株式会社 | Thick high-strength steel sheet excellent in brittle crack propagation stopping characteristics and method for producing the same |
| JP5713135B1 (en) | 2013-11-19 | 2015-05-07 | 新日鐵住金株式会社 | steel sheet |
| KR20160075927A (en) | 2014-12-19 | 2016-06-30 | 주식회사 포스코 | The steel sheet having excellent strength and toughness at the center of thickness and method for manufacturing the same |
-
1982
- 1982-09-10 JP JP15679682A patent/JPS5947323A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5947323A (en) | 1984-03-17 |
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