JPH0569902B2 - - Google Patents

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Publication number
JPH0569902B2
JPH0569902B2 JP31467089A JP31467089A JPH0569902B2 JP H0569902 B2 JPH0569902 B2 JP H0569902B2 JP 31467089 A JP31467089 A JP 31467089A JP 31467089 A JP31467089 A JP 31467089A JP H0569902 B2 JPH0569902 B2 JP H0569902B2
Authority
JP
Japan
Prior art keywords
steel
toughness
oxides
haz
oxide
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 - Fee Related
Application number
JP31467089A
Other languages
Japanese (ja)
Other versions
JPH03177535A (en
Inventor
Toshinaga Hasegawa
Koichi Yamamoto
Shuji Aihara
Kentaro Okamoto
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP31467089A priority Critical patent/JPH03177535A/en
Publication of JPH03177535A publication Critical patent/JPH03177535A/en
Publication of JPH0569902B2 publication Critical patent/JPH0569902B2/ja
Granted legal-status Critical Current

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Description

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

(産業上の利用分野) 本発明は溶接入熱が200kJ/cm程度の大入熱溶
接に至る広範な入熱の溶接においても、良好な溶
接熱影響部の低温靭性を有する溶接用低温高靭性
鋼の製造方法にかかわるものである。 (従来の技術) 近年、海洋構造物、船舶等、大型構造物の材質
に対する要求は安全性確保の点から厳しさを増し
ている。特に母材に比べて材質が劣化する傾向に
ある溶接熱影響部の低温靭性の向上が望まれてい
る。一般に鋼材をサブマージアーク溶接やエレク
トロスラグ溶接などの溶接入熱の大きい自動溶接
を行うと、溶接熱影響部(以下、HAZと称する)
のオーステナイト結晶粒が粗大化することにより
HAZの組織が粗くなり、HAZ靭性が著しく低下
する。 HAZ靭性向上のためにはHAZ、特に高温にさ
らされる融合部(フユージヨンライン、以下FL
と称する)近傍のHAZ組織を微細化する必要が
あり、従来、以下に示すような種々のHAZ組織
微細化方法が提案されている。 例えば、昭和54年6月発行の「鉄と鋼」第65巻
第8号1232頁においては、TiNを微細析出させ
ることによりHAZのオーステナイト粒を微細化
して、50Kgf/mm2級高張力鋼の大入熱溶接時の
HAZ靭性を改善する技術が開示されているが、
TiNはFL直近では溶接時に大部分が溶解し、オ
ーステナイトの粗粒化と固溶Nの増加とにより、
HAZ靭性の劣化が避けられないという欠点が存
在する。 ごく最近では、例えば特開昭61−117213号公報
に見られるように、オーステナイトの細粒化によ
らずに粒内フエライトを生成させることにより、
HAZ組織の微細化を図る技術が開発されている。
本発明者らの一部は粒内フエライトの生成核とし
てTi酸化物が有効であり、Ti酸化物は高温にさ
らされても溶解することがなく、FL直近でも粒
内フエライトの核として働き、組織微細化が可能
で、TiN等を利用した鋼に比較してFL近傍の
HAZ靭性の著しい改善が可能であることを、例
えば特開昭61−117245号公報に示した。 (発明が解決しようとする課題) Ti酸化物を粒内フエライトの変態核とした場
合は、TiNや他の複合単窒化物等を核とした場
合に比べて高温安定性には優れているが、酸化物
であるため、凝固時にその分散状態が決定され、
単窒化物に比べて分散状態の制御が困難であり、
またTi酸化物の個数自体も現状の製鋼、凝固法
においてはTiN等と比べて非常に少ないなどの
問題がある。 さらに、粗大なTi酸化物ができやすく、その
場合には酸化物自身が脆性破壊の起点となつて
HAZ靭性劣化を招く。従つて、酸化物を用いた
鋼材で安定したHAZ靭性を確保し、一層のHAZ
靭性向上を図るためには粒内フエライトの核とな
り得る酸化物を微細、多量且つ均一に分布できる
手法が必要となる。 本発明は過酷な使用条件に対して安全性の高い
溶接用低温高靭性鋼の製造方法を提供するもので
ある。 (課題を解決するための手段) 本発明は鋼中に安定して微細分散し、且つ粒内
フエライトの生成核となる酸化物の検討を種々行
つた結果発明に至つたものであり、その要旨とす
るところは、C:0.02〜0.18%、Si:0.5%以下、
Mn:0.4〜2.0%、S:0.001〜0.01%、N:0.006
%以下、Al:0.006%以下を基本成分とし、必要
に応じてさらに、Cr:1.0%以下、Ni:3.0%以
下、Mo:0.5%以下、V:0.1%以下、Nb:0.05
%以下、Cu:1.5%以下の1種または2種以上を
含有し、不純物としてP:0.015%以下、残部は
Fe及び不可避不純物からなる溶鋼中のO量を
0.0030〜0.015%とし、TiとYをTi:0.005〜0.020
%、Y:0.0010〜0.010%の範囲で添加後、凝固
させることを特徴とする溶接用低温高靭性鋼の製
造方法にある。 (作用) 本発明はFL直近の高温にさらされるHAZにお
いても、安定に存在し得る酸化物の内で、粒内フ
エライトの生成核として有効に働き、且つ従来の
Ti酸化物を利用した鋼以上に鋼中に安定して、
多量に均一微細分散し、HAZ靭性を著しく改善
することができる酸化物を含む鋼について種々検
討した結果、発明に至つたものである。 以下、本発明の要旨を実験結果に基づいて詳細
に説明する。 本発明者らはC:0.06%、Si:0.1%、Mn:1.4
%、Ni:0.3%、Cu:0.3%、Nb:0.015%、P:
0.005%、S:0.0030%、N:0.003%程度の化学
成分を有する鋼を真空溶解炉で溶製し、Ti酸化
物及び種々の酸化物を鋼中に分散させることを目
的として、出鋼前5〜10分の間にTiを約0.015%
添加し、さらに以下にのべる1種類の元素を
0.0050〜0.010%の範囲で添加した後、鋳型に鋳
込んで重量25Kgのインゴツトとした。 Ti以外の添加元素としてはLa、Ca、Ce、Yを
選んだ。 各々のインゴツトを熱間圧延し、焼入れ焼戻し
処理を加えて素材とした。素材より採取した試験
片にFL近傍のHAZの受ける熱履歴をシミユレー
トした溶接再現熱サイクルを加えた。 溶接再現熱サイクル条件は加熱温度1400℃、保
持時間1秒で、800〜500℃までの冷却時間
(Δ8/5)がサブマージアーク(SAW)溶接の中入
熱溶接に相当する40秒と大入熱溶接に相当する
161秒の2種類とした。 再現熱サイクルを施した後、酸化物の調査及び
2mmVノツチシヤルピー特性を調査した。 先ず、抽出レプリカの電子顕微鏡観察により酸
化物の調査を行つた結果、Ti以外にはLa、Ca、
Ce、Yを複合添加した鋼において、鋼中に含ま
れる主要な酸化物は、何れもTiと添加したもう
一つの元素の複合酸化物であることが判明した。 複合酸化物の分布状態は第1図に示す通りで、
TiとYの複合酸化物が他の複合酸化物に比べて、
粒子径が2.0μm以下の微細な酸化物個数が多く、
平均サイズも小さい。 即ち、同一の溶解、凝固条件で比較した場合、
TiとYの複合酸化物は、従来からHAZ靭性改善
に有効として用いられているTi単独の酸化物よ
りも一層、微細分散が可能であることが判明し
た。 第2図、第3図に0.1〜2.0μmの粒子径の酸化
物個数とシヤルピー特性(50%破面遷移温度:
vTrs)の関係を調べた結果を示す。 TiとCeの複合酸化物以外はTi単独の酸化物も
含めて、0.1〜2.0μmの粒子径の酸化物個数と
vTrsは概略直線関係にあり、酸化物個数が増加
するにつれてvTrsは向上し、酸化物が微細分散
する分、TiとYの複合酸化物の方がTi単独酸化
物によるよりも一層のHAZ靭性向上が図れる。
TiとCeの複合酸化物は比較的多量且つ微細分散
するが、熱サイクル組織に粒内フエライトの生成
が認められず、靭性も低い。 即ち、TiとCeの複合酸化物は粒内フエライト
生成能を有しないため、有効でない。その他は何
れも粒内フエライト生成能を有するが、TiとLa
の複合参加は個数が非常に少ないため、第2図、
第3図の熱サイクル条件においては粒内フエライ
トの生成量が少なく、靭性は著しく劣つている。 以上の実験結果から酸化物を用いた鋼材で安定
したHAZ靭性を確保し、Ti酸化物を利用した鋼
以上の一層のHAZ靭性向上を図るための方法と
して、TiとYを溶鋼中に添加することにより、
粒内フエライトの核となり、且つ微細、多量且つ
均一に分布できるTiとYの複合酸化物を形成さ
せることが極めて有効であるとの結論に至つた。 なお、本発明におけるTiとYの複合酸化物と
は、TiとYとOを主要元素とする酸化物のこと
で、この酸化物には鋼中や原料の不純物から持ち
きたされる他の元素が微量に含まれることもある
が、これらの元素もフエライト生成能を有する限
りはTiとYの複合酸化物に包含する。 具体的には微量のFe、Mn、Ca、Al等がTi、
Y、O以外に含有される場合が多いが、何れも十
分な粒内フエライト生成能を有する。 TiとYの量は、以下に述べる理由から、添加
量として溶鋼重量に対し、Ti:0.005〜0.020%、
Y:0.0010〜0.010%の範囲が好ましい。 先ず、Tiは0.005%未満では必要な酸化物量が
確保できないので、0.005%以上は必要である。
TiはTiとYの複合酸化物を形成する以外に、
TiNを形成することによつて、母材の加熱オー
ステナイトの細粒化や、HAZのFLから遠い領域
でのオーステナイト細粒化を生じさせ、母材、
HAZの靭性向上に有効であるので、酸化物を形
成する量以上に含有させることが可能であるが、
0.020%を超えると粗大なTiNが形成されたり、
析出脆化を生じる恐れがあるため、0.005〜0.020
%の範囲とした。 次に、YはTiと複合酸化物を形成することに
より、酸化物の均一微細分散を可能にしている元
素で、多量の添加は不要であるが、0.0010%以上
添加しないと十分な効果が得られない。一方、
0.010%を超える添加では粗大な酸化物を生じて、
酸化物の微細分散に有効でなく、さらに靭性上も
好ましくないので、0.0010〜0.010%の範囲とし
た。 TiとYの添加手段は、溶鋼に純チタンもしく
はチタン合金及び純イツトリウムもしくはイツト
リウムを含む母合金を、同時にあるいは順次添加
して鋳造・凝固させる手段でもよいし、予め前記
粒度の範囲内に調整したTiとYの複合酸化物を
溶鋼に噴射添加し、そのまま、鋳造・凝固させて
もよい。TiとYの添加順序は問わない。 加えて、TiとYの複合酸化物は溶鋼中にTiと
Yを添加することによつて形成されるので、Ti
とYを添加するときのO濃度が重要となる。本発
明者らの検討結果によれば、Oが0.0030%未満で
は粒内フエライト生成に十分なTiとYの複合酸
化物が形成され難い。 一方、0.015%を超えたO濃度の溶鋼中にTi、
Yを添加すると、粗大な酸化物を形成して、複合
酸化物の数が減少するとともに、粗大な酸化物が
破壊の起点となることにより靭性が劣化するよう
になる。従つて、TiとYを添加するときの溶鋼
中のO濃度は0.005〜0.015%とする必要がある。 凝固後の鋼材は何らかの手段により、所望の形
状とするが、鋼材は通常の圧延ままのもの、制御
圧延をしたもの、さらにこれに制御冷却と焼戻し
を加えたもの、及び焼入れ・焼戻しまたは焼なら
し及び両者を組み合わせたものであつても、該酸
化物の効果は何ら影響を受けることはない。 次に、本発明鋼の基本成分範囲の限定理由につ
いて述べる。 先ず、Cは鋼の強度を向上させる有効な成分と
して添加するもので、0.02%未満では構造溶鋼に
必要な強度の確保が困難であり、また、0.18%を
超える過剰の添加は耐溶接割れ性などを著しく低
下させるので、0.02〜0.18%の範囲とした。 次に、Siは母材の強度確保に有効な元素である
が、0.5%を超える過剰の添加はHAZに高炭素島
状マルテンサイトを生成して靭性を低下させるた
め、上限を0.5%とした。 また、Mnは母材の強度靭性の確保に必要な元
素であり、最低限0.4%以上添加する必要がある
が、溶接部の靭性、割れ性など許容できる範囲で
上限を2.0%とした。 一方、Pは母材、溶接部との靭性に悪影響を及
ぼすので、極力低減するべきであり、上限を
0.015%とした。 SについてはMnSを形成して粒内フエライト
生成を助長する元素であるので、0.001%以上必
要であるが、0.01%を超える過剰の添加は粗大な
A系介在物を形成して母材の延性、靭性の低下と
機械的性質の異方性の増加を招く上から避けるべ
きであり、従つて、Sは0.001〜0.01%の範囲と
した。 NはTiNとして母材の細粒化に寄与するが、
特に大入熱溶接時に高炭素島状マルテンサイトを
生成して靭性を低下させるため、上限を0.006%
とした。 Alは通常の鋼では脱酸、母材の細粒化等に必
要が元素であるが、通常アルミキルド程度の添加
でも溶鋼酸素量を著しく低下させ、フエライト生
成核となるTiとYの複合酸化物の形成が難しく
なるため、上限を0.006%とした。 以上が本発明鋼の基本成分であるが、母材強度
の上昇、母材及びHAZ靭性向上の目的で、必要
に応じてCr、Ni、Mo、V、Nb、Cuの1種また
は2種以上を含有することができる。 先ず、Niは母材の強度、靭性とHAZの靭性を
同時に向上できる極めて有効な元素であるが、
3.0%を超す過剰の添加をすると焼入性の増加に
より本発明鋼に必要な粒内フエライトの形成が抑
制され、HAZ靭性が劣化するため、上限を3.0%
とした。 次に、Cuは母材強度を高める割にはHAZの硬
さ上昇が少ないという点で有効な元素であるが、
応力除去焼鈍によるHAZの硬化、靭性劣化の恐
れがあることから、上限を1.5%とした。 さらにCr、Mo、V、Nbは焼入性の向上と析
出硬化により母材の強度上昇に有効な元素である
が、上限値を超える添加はHAZ靭性の劣化を招
くので、Cr、Mo、V、Nbのそれぞれについて
上限を1.0%、0.5%、0.1%、0.05%とした。 次に、本発明の効果を実施例によつてさらに具
体的に述べる。 (実施例) 第1表に本発明に従つて試作した鋼及び比較鋼
の化学成分、Ti、Y等の酸化物形成元素の種類、
添加量、酸化物のサイズ、個数、溶接部の靭性等
を示す。 ここで、No.1〜No.10が本発明鋼であり、No.11〜
No.16が比較鋼である。 本発明鋼、比較鋼とも圧延により20mm及び30mm
の鋼板とした。 20mm材についてはX開先で、電流700A、電圧
32V、溶接速度30cm/min、入熱45kJ/cmの両面
1層1電極潜弧溶接(サブマージアーク溶接)を
行つた。 30mm材についてはY開先で、電流1380A(L
極)、1150A(T1極)、1040A(T2極)、電圧36V
(L極)、42V(T1極)、46V(T2極)、溶接速度45
cm/min、入熱194kJ/cmの片面1層3電極サブ
マージアーク溶接を行い、いずれも2mmVノツチ
シヤルピー衝撃試験片を板表面から7mmの位置が
試験片の中心部となり、溶接金属とHAZの境界
(融合部:FL)からHAZ側に1mm入つた位置が
ノツチ位置となるよう採取し、60℃で試験を実施
した。
(Industrial Application Field) The present invention provides a low-temperature high-toughness welding material that has good low-temperature toughness of the weld heat-affected zone even in welding with a wide range of heat inputs, including large heat input welding with a welding heat input of about 200 kJ/cm. It is related to the method of manufacturing steel. (Prior Art) In recent years, requirements for materials for large structures such as offshore structures and ships have become increasingly strict from the standpoint of ensuring safety. In particular, it is desired to improve the low-temperature toughness of the weld heat-affected zone, which tends to deteriorate in quality compared to the base metal. Generally, when steel materials are subjected to automatic welding with a large welding heat input such as submerged arc welding or electroslag welding, the weld heat affected zone (hereinafter referred to as HAZ)
By coarsening the austenite grains of
The structure of the HAZ becomes coarse and the HAZ toughness decreases significantly. In order to improve HAZ toughness, HAZ, especially the fusion line (hereinafter FL) exposed to high temperatures, must be
There is a need to refine the HAZ structure in the vicinity (referred to as . For example, in "Tetsu to Hagane" Vol. 65, No. 8, p. 1232, published in June 1978, the austenite grains in HAZ were refined by finely precipitating TiN, and 50Kgf/mm grade 2 high-strength steel was produced. During large heat input welding
Although techniques for improving HAZ toughness have been disclosed,
Most of TiN melts during welding in the vicinity of the FL, and due to the coarsening of austenite and the increase in solute N,
There is a drawback that deterioration of HAZ toughness is unavoidable. Very recently, as seen in JP-A-61-117213, for example, by generating intragranular ferrite without refining austenite,
Techniques have been developed to refine the HAZ structure.
Some of the present inventors believe that Ti oxide is effective as a generation nucleus for intragranular ferrite, that Ti oxide does not dissolve even when exposed to high temperatures, and that it acts as a nucleus for intragranular ferrite even in the vicinity of the FL. It is possible to refine the structure, and compared to steels using TiN etc.
For example, it was shown in JP-A-61-117245 that HAZ toughness can be significantly improved. (Problem to be solved by the invention) When Ti oxide is used as the transformation nucleus of intragranular ferrite, it has better high-temperature stability than when TiN or other composite mononitrides are used as the nucleus. , since it is an oxide, its dispersion state is determined during solidification,
It is difficult to control the dispersion state compared to mononitrides,
Furthermore, there are problems in that the number of Ti oxides itself is very small compared to TiN etc. in the current steel manufacturing and solidification methods. Furthermore, coarse Ti oxides tend to form, and in that case, the oxide itself becomes the starting point for brittle fracture.
This leads to deterioration of HAZ toughness. Therefore, steel materials using oxides ensure stable HAZ toughness and further improve HAZ
In order to improve toughness, a method is required that can uniformly distribute oxides that can form the nucleus of intragranular ferrite in a fine, large amount and uniformly. The present invention provides a method for producing a low-temperature, high-toughness steel for welding that is highly safe under severe usage conditions. (Means for Solving the Problems) The present invention was developed as a result of various studies on oxides that are stably and finely dispersed in steel and that serve as nuclei for the formation of intragranular ferrite. Where C: 0.02 to 0.18%, Si: 0.5% or less,
Mn: 0.4-2.0%, S: 0.001-0.01%, N: 0.006
% or less, Al: 0.006% or less as a basic component, and if necessary further added: Cr: 1.0% or less, Ni: 3.0% or less, Mo: 0.5% or less, V: 0.1% or less, Nb: 0.05
% or less, Cu: contains one or more of 1.5% or less, P: 0.015% or less as impurities, the remainder is
The amount of O in molten steel consisting of Fe and unavoidable impurities
0.0030~0.015%, Ti and Y: 0.005~0.020
%, Y: in the range of 0.0010 to 0.010%, and then solidified. (Function) The present invention effectively functions as a generation nucleus for intragranular ferrite among oxides that can stably exist even in the HAZ exposed to high temperatures near the FL, and
More stable in steel than steel using Ti oxide,
The invention was developed as a result of various studies on steel containing oxides that can be uniformly and finely dispersed in large amounts and significantly improve HAZ toughness. Hereinafter, the gist of the present invention will be explained in detail based on experimental results. The present inventors found that C: 0.06%, Si: 0.1%, Mn: 1.4
%, Ni: 0.3%, Cu: 0.3%, Nb: 0.015%, P:
Steel having a chemical composition of about 0.005%, S: 0.0030%, N: 0.003% is melted in a vacuum melting furnace, and the purpose of dispersing Ti oxide and various oxides in the steel is to melt the steel before tapping. Approximately 0.015% Ti for 5-10 minutes
Add one type of element listed below.
After adding it in a range of 0.0050 to 0.010%, it was cast into a mold to form an ingot weighing 25 kg. La, Ca, Ce, and Y were selected as additive elements other than Ti. Each ingot was hot rolled and subjected to quenching and tempering treatment to obtain a material. A welding reproduction thermal cycle was applied to the test piece taken from the material, simulating the thermal history experienced by the HAZ near the FL. The welding reproduction thermal cycle conditions are a heating temperature of 1400℃, a holding time of 1 second, and a cooling time (Δ 8/5 ) from 800 to 500℃ of 40 seconds, which is equivalent to medium heat input welding of submerged arc (SAW) welding. Equivalent to heat input welding
There are two types of 161 seconds. After repeated thermal cycling, the oxide and 2 mm V notch characteristics were investigated. First, we investigated oxides by observing the extracted replica with an electron microscope, and found that in addition to Ti, there were La, Ca,
It has been found that in steels with combined addition of Ce and Y, the main oxides contained in the steel are all composite oxides of Ti and another element added. The distribution state of the composite oxide is as shown in Figure 1.
Compared to other composite oxides, Ti and Y composite oxides are
There are many fine oxides with a particle size of 2.0μm or less,
The average size is also small. That is, when compared under the same dissolution and solidification conditions,
It has been found that the composite oxide of Ti and Y can be dispersed more finely than the oxide of Ti alone, which has traditionally been used to improve HAZ toughness. Figures 2 and 3 show the number of oxides with a particle size of 0.1 to 2.0 μm and the shear pi properties (50% fracture surface transition temperature:
vTrs). The number of oxides with a particle size of 0.1 to 2.0 μm, except for composite oxides of Ti and Ce, including oxides of Ti alone.
vTrs has an approximately linear relationship, and as the number of oxides increases, vTrs improves, and because the oxides are finely dispersed, the composite oxide of Ti and Y improves the HAZ toughness even more than the single oxide of Ti. can be achieved.
Although the composite oxide of Ti and Ce is dispersed in a relatively large amount and finely, the formation of intragranular ferrite is not observed in the thermal cycle structure, and the toughness is low. That is, the composite oxide of Ti and Ce does not have the ability to generate intragranular ferrite, and is therefore not effective. All of the others have the ability to generate intragranular ferrite, but Ti and La
Since the number of multiple participants is very small, Figure 2,
Under the thermal cycle conditions shown in FIG. 3, the amount of intragranular ferrite produced is small, and the toughness is significantly inferior. Based on the above experimental results, adding Ti and Y to molten steel is a method to ensure stable HAZ toughness in steel materials using oxides and to further improve HAZ toughness than steels using Ti oxides. By this,
It was concluded that it is extremely effective to form a composite oxide of Ti and Y that serves as the core of intragranular ferrite and can be distributed finely, in large quantities, and uniformly. In addition, the composite oxide of Ti and Y in the present invention is an oxide whose main elements are Ti, Y, and O, and this oxide contains other elements brought in from impurities in the steel and raw materials. may be contained in trace amounts, but these elements are included in the composite oxide of Ti and Y as long as they have the ability to form ferrite. Specifically, trace amounts of Fe, Mn, Ca, Al, etc.
It is often contained in addition to Y and O, but both have sufficient ability to generate intragranular ferrite. For the reasons described below, the amount of Ti and Y added is 0.005% to 0.020% based on the weight of molten steel.
Y: The range is preferably 0.0010% to 0.010%. First, if Ti is less than 0.005%, the necessary oxide amount cannot be secured, so 0.005% or more is necessary.
In addition to forming a composite oxide of Ti and Y, Ti
By forming TiN, the heated austenite in the base metal becomes finer, and the austenite becomes finer in the region far from the FL of the HAZ.
Since it is effective in improving the toughness of the HAZ, it is possible to contain it in an amount exceeding the amount that forms oxides.
If it exceeds 0.020%, coarse TiN may be formed,
0.005 to 0.020 as there is a risk of precipitation embrittlement.
% range. Next, Y is an element that enables uniform and fine dispersion of the oxide by forming a composite oxide with Ti, and although it is not necessary to add a large amount, sufficient effects cannot be obtained unless it is added in an amount of 0.0010% or more. I can't. on the other hand,
Addition of more than 0.010% produces coarse oxides,
Since it is not effective for fine dispersion of oxides and is also unfavorable in terms of toughness, it is set in the range of 0.0010 to 0.010%. The means for adding Ti and Y may be a method in which pure titanium or a titanium alloy and pure yttrium or a master alloy containing yttrium are added to molten steel simultaneously or sequentially and then cast and solidified, or by adjusting the particle size in advance within the above range. A composite oxide of Ti and Y may be added to molten steel by injection, and the molten steel may be directly cast and solidified. The order of addition of Ti and Y does not matter. In addition, since composite oxides of Ti and Y are formed by adding Ti and Y to molten steel, Ti
The O concentration when adding Y and Y is important. According to the study results of the present inventors, when O is less than 0.0030%, it is difficult to form a composite oxide of Ti and Y sufficient for intragranular ferrite formation. On the other hand, Ti in molten steel with an O concentration exceeding 0.015%
When Y is added, coarse oxides are formed, the number of composite oxides decreases, and toughness deteriorates as the coarse oxides become a starting point for fracture. Therefore, when adding Ti and Y, the O concentration in the molten steel needs to be 0.005 to 0.015%. After solidification, the steel material is shaped into the desired shape by some means, and the steel material may be as-rolled, controlled-rolled, controlled-cooled and tempered, or quenched, tempered, or tempered. Even if the oxide is used or a combination of the two is used, the effect of the oxide is not affected in any way. Next, the reason for limiting the basic component range of the steel of the present invention will be described. First of all, C is added as an effective component to improve the strength of steel; if it is less than 0.02%, it is difficult to secure the strength required for structural molten steel, and if it is added in excess of 0.18%, it may reduce the weld cracking resistance. Because it significantly reduces the Next, although Si is an effective element for ensuring the strength of the base metal, excessive addition of more than 0.5% will generate high carbon island martensite in the HAZ and reduce toughness, so the upper limit was set at 0.5%. . In addition, Mn is an element necessary to ensure the strength and toughness of the base metal, and must be added at least 0.4%, but the upper limit was set at 2.0% as long as it was acceptable for the toughness and crackability of the welded part. On the other hand, P has a negative effect on the toughness of the base metal and weld, so it should be reduced as much as possible, and the upper limit should be
It was set as 0.015%. S is an element that forms MnS and promotes intragranular ferrite formation, so 0.001% or more is required, but excessive addition of more than 0.01% may form coarse A-based inclusions and reduce the ductility of the base metal. S should be avoided because it causes a decrease in toughness and an increase in anisotropy of mechanical properties. Therefore, S is set in the range of 0.001 to 0.01%. N contributes to grain refinement of the base material as TiN, but
In particular, during high heat input welding, high carbon island martensite is generated and toughness is reduced, so the upper limit has been set to 0.006%.
And so. Al is an element necessary for deoxidation and grain refinement of the base material in ordinary steel, but even when added to the normal level of aluminum kill, it significantly reduces the amount of oxygen in molten steel and forms a composite oxide of Ti and Y that becomes the nucleus for ferrite formation. The upper limit was set at 0.006%. The above are the basic components of the steel of the present invention, but one or more of Cr, Ni, Mo, V, Nb, and Cu may be added as necessary for the purpose of increasing base metal strength and improving base metal and HAZ toughness. can contain. First of all, Ni is an extremely effective element that can simultaneously improve the strength and toughness of the base metal and the toughness of the HAZ.
If excessive addition exceeds 3.0%, the hardenability will increase and the formation of intragranular ferrite, which is necessary for the steel of the present invention, will be suppressed and the HAZ toughness will deteriorate, so the upper limit is set at 3.0%.
And so. Next, Cu is an effective element in that it does not increase the hardness of HAZ even though it increases the strength of the base metal.
The upper limit was set at 1.5% due to the risk of hardening of the HAZ and deterioration of toughness due to stress relief annealing. Furthermore, Cr, Mo, V, and Nb are effective elements for increasing the strength of the base metal by improving hardenability and precipitation hardening, but addition exceeding the upper limit causes deterioration of HAZ toughness, so Cr, Mo, , Nb were set at 1.0%, 0.5%, 0.1%, and 0.05%, respectively. Next, the effects of the present invention will be described in more detail with reference to Examples. (Example) Table 1 shows the chemical composition of steel prototyped according to the present invention and comparative steel, types of oxide-forming elements such as Ti and Y,
Indicates the amount added, the size and number of oxides, the toughness of the weld, etc. Here, No. 1 to No. 10 are the steels of the present invention, and No. 11 to No. 10 are the steels of the present invention.
No.16 is the comparison steel. Both the invention steel and comparative steel are 20mm and 30mm by rolling.
steel plate. For 20mm material, X groove, current 700A, voltage
Double-sided, single-layer, single-electrode latent arc welding (submerged arc welding) was performed at 32V, welding speed of 30cm/min, and heat input of 45kJ/cm. For 30mm material, Y groove, current 1380A (L
pole), 1150A (T1 pole), 1040A (T2 pole), voltage 36V
(L pole), 42V (T1 pole), 46V (T2 pole), welding speed 45
Single-sided, single-layer, three-electrode submerged arc welding with a heat input of 194 kJ/cm and a heat input of 194 kJ/cm was performed, and a 2 mm V notched pylon impact test piece was placed at the center of the test piece at a position 7 mm from the plate surface, and the boundary between the weld metal and the HAZ ( A sample was taken so that the notch position was 1 mm from the fusion part (FL) to the HAZ side, and the test was conducted at 60°C.

【表】【table】

【表】【table】

【表】 第1表から明らかなように、本発明鋼は比較鋼
に比べて優れたHAZ靭性を有し、−60℃の低温で
も構造物の安全性確保に十分なシヤルピー試験の
吸収エネルギーを示すことが分かる。即ち、本発
明鋼はいずれもOを0.0030〜0.015%とした溶鋼
中にTiとYを添加することにより0.1〜2.0μm径
の微細なTiとYの複合酸化物が多量に鋼中に分
散しており、その結果として、入熱40kJ/cmの
両面1層溶接だけでなく、入熱194kJ/cmの片面
1層大入熱溶接においても極めて優れたシヤルピ
ー特性を示している。 一方、比較鋼においてNo.11、No.12はTi単独の
酸化物を分散させた鋼であるが、No.11は酸化物個
数が十分確保できておらず、またNo.12は2.0μmを
超える酸化物が存在するために、何れも本発明鋼
に比べてHAZ靭性が若干劣る。比較鋼No.113〜No.
15は複合酸化物を含有する鋼であるが、複合酸化
物がTiとYの複合酸化物ではないため、酸化物
数が不十分であつたり、酸化物自体に粒内フエラ
イト生成能がないために極めて低い靭性値となつ
ている。比較鋼No.16はAlを含有した鋼で、Ti酸
化物は少なく、TiNにより組織の微細化を図つ
た鋼であるが、FL直近でTiNが溶解してオース
テナイオ粒径の粗大化が生じ、固溶N量も増加し
たためにFL近傍のHAZ靭性は本発明鋼に比べて
劣つている。 以上の実施例から本発明によれば、200kJ/cm
程度の大入熱溶接に至るまで、−60℃でも十分な
吸収エネルギーを示す、極めて優れたHAZ靭性
が得られることが明白である。 (発明の効果) Ti酸化物を利用してHAZ組織に粒内フエライ
トを生成させて組織の微細化を図る技術は、
HAZ靭性向上のための優れた技術である。本発
明に従えばTiとYの複合酸化物の微細分散によ
り、Ti酸化物によるよりも一層のHAZ靭性向上
が図れることが以上の実施例からも明らかであ
る。 従つて、本発明は、より過酷な使用条件に対し
ても安全性の高い溶接構造用低温高靭性鋼を提供
することを可能とするものであり、その効果は極
めて顕著である。
[Table] As is clear from Table 1, the steel of the present invention has superior HAZ toughness compared to comparative steels, and absorbs enough energy in the Charpy test to ensure the safety of structures even at temperatures as low as -60°C. I understand what is shown. That is, in all of the steels of the present invention, by adding Ti and Y to molten steel containing 0.0030 to 0.015% O, a large amount of fine composite oxides of Ti and Y with a diameter of 0.1 to 2.0 μm is dispersed in the steel. As a result, it shows extremely excellent shear strength properties not only in double-sided, single-layer welding with a heat input of 40 kJ/cm, but also in single-sided, single-layer large heat input welding with a heat input of 194 kJ/cm. On the other hand, among comparative steels, No. 11 and No. 12 are steels in which Ti oxide alone is dispersed, but No. 11 does not have a sufficient number of oxides, and No. 12 has a 2.0 μm In both cases, the HAZ toughness is slightly inferior to that of the steel of the present invention due to the presence of oxides exceeding the above. Comparative steel No.113~No.
15 is a steel containing a composite oxide, but because the composite oxide is not a composite oxide of Ti and Y, the number of oxides is insufficient, or the oxide itself does not have the ability to generate intragranular ferrite. The toughness value is extremely low. Comparison steel No. 16 is a steel that contains Al, has little Ti oxide, and has a finer structure with TiN, but the TiN melts near the FL and coarsens the austenio grain size. , the HAZ toughness near the FL is inferior to that of the steel of the present invention due to the increased amount of solid solute N. From the above embodiments, according to the present invention, 200kJ/cm
It is clear that extremely excellent HAZ toughness, which shows sufficient absorbed energy even at -60°C, can be obtained up to moderately high heat input welding. (Effects of the invention) The technology that uses Ti oxide to generate intragranular ferrite in the HAZ structure to refine the structure is as follows:
This is an excellent technology for improving HAZ toughness. It is clear from the above examples that according to the present invention, by finely dispersing the composite oxide of Ti and Y, the HAZ toughness can be further improved than by using Ti oxide. Therefore, the present invention makes it possible to provide a low-temperature, high-toughness steel for welded structures that is highly safe even under harsher usage conditions, and its effects are extremely significant.

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

第1図は鋼中に含有される各種複合酸化物の粒
子径と粒子数の関係を示す図表、第2図は酸化物
粒子数とΔ8/5=40秒の溶接再現熱サイクルを加え
たときのシヤルピー特性の関係を示す図表、第3
図は酸化物粒子数とΔ8/5=161秒の溶接再現熱サ
イクルを加えたときのシヤルピー特性の関係を示
す図表である。
Figure 1 is a chart showing the relationship between the particle size and number of particles of various composite oxides contained in steel, and Figure 2 is a graph showing the relationship between the number of oxide particles and the simulated welding thermal cycle of Δ 8/5 = 40 seconds. Chart showing the relationship between the Charpey characteristics when
The figure is a chart showing the relationship between the number of oxide particles and the shear pie characteristics when a welding reproduction thermal cycle of Δ 8/5 = 161 seconds is applied.

Claims (1)

【特許請求の範囲】 1 重量%で C:0.02〜0.18% Si:0.5%以下 Mn:0.4〜2.0% S:0.001〜0.01% N:0.006%以下 Al:0.006%以下 を基本成分とし、不純物としてP:0.015%以下、
残部はFe及び不可避不純物からなる溶鋼中のO
量を0.0030〜0.015%とし、TiとYをTi:0.005〜
0.020%、Y:0.0010〜0.010%の範囲で添加後、
凝固させることを特徴とする溶接用低温高靭性鋼
の製造方法。 2 重量%で Cr:1.0%以下 Ni:3.0%以下 Mo:0.5%以下 V:0.1%以下 Nb:0.05%以下 Cu:1.5%以下 の1種または2種以上を含有することを特徴とす
る特許請求の範囲第1項記載の溶接用低温高靭性
鋼の製造方法。
[Claims] 1 In terms of weight%, C: 0.02 to 0.18% Si: 0.5% or less Mn: 0.4 to 2.0% S: 0.001 to 0.01% N: 0.006% or less Al: 0.006% or less as basic components, and as impurities P: 0.015% or less,
The remainder is O in molten steel consisting of Fe and unavoidable impurities.
The amount is 0.0030-0.015%, and Ti and Y are Ti: 0.005-0.005%.
After adding 0.020%, Y: in the range of 0.0010 to 0.010%,
A method for producing a low-temperature high-toughness steel for welding, characterized by solidifying it. 2. A patent characterized by containing one or more of the following in weight%: Cr: 1.0% or less Ni: 3.0% Mo: 0.5% or less V: 0.1% or less Nb: 0.05% or less Cu: 1.5% or less A method for producing a low-temperature high-toughness steel for welding according to claim 1.
JP31467089A 1989-12-04 1989-12-04 Manufacture of low temperature high toughness steel for welding Granted JPH03177535A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31467089A JPH03177535A (en) 1989-12-04 1989-12-04 Manufacture of low temperature high toughness steel for welding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31467089A JPH03177535A (en) 1989-12-04 1989-12-04 Manufacture of low temperature high toughness steel for welding

Publications (2)

Publication Number Publication Date
JPH03177535A JPH03177535A (en) 1991-08-01
JPH0569902B2 true JPH0569902B2 (en) 1993-10-04

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Family Applications (1)

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Country Status (1)

Country Link
JP (1) JPH03177535A (en)

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Publication number Priority date Publication date Assignee Title
JP2940647B2 (en) * 1991-08-14 1999-08-25 新日本製鐵株式会社 Method for producing low-temperature high-toughness steel for welding
JP2653594B2 (en) * 1991-12-18 1997-09-17 新日本製鐵株式会社 Manufacturing method of thick steel plate with excellent toughness of weld heat affected zone
JP3802810B2 (en) * 1999-10-12 2006-07-26 新日本製鐵株式会社 Steel for welded structures having no dependence on heat input of HAZ toughness and method for manufacturing
KR100368242B1 (en) * 2000-08-02 2003-02-06 주식회사 포스코 Steel plate having superior toughness in weld heat-affected zone and method for manufacturing the same, welding fabric using the same
KR200448270Y1 (en) * 2007-10-30 2010-03-29 주식회사 지비 Breakers and Excavators for Excavators
CN112011739B (en) * 2020-08-27 2021-08-06 江苏大学 A kind of high toughness iron alloy and its preparation method and application

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