JP2002003986A - High tensile steel for large heat input welding - Google Patents

High tensile steel for large heat input welding

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Publication number
JP2002003986A
JP2002003986A JP2000184986A JP2000184986A JP2002003986A JP 2002003986 A JP2002003986 A JP 2002003986A JP 2000184986 A JP2000184986 A JP 2000184986A JP 2000184986 A JP2000184986 A JP 2000184986A JP 2002003986 A JP2002003986 A JP 2002003986A
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JP
Japan
Prior art keywords
steel
heat input
haz
particles
welding
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.)
Granted
Application number
JP2000184986A
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Japanese (ja)
Other versions
JP3782645B2 (en
Inventor
Manabu Hoshino
学 星野
Naoki Saito
直樹 斎藤
Ryuji Uemori
龍治 植森
Toshimichi Nagao
年道 長尾
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Nippon Steel Corp
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Nippon Steel Corp
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Priority to JP2000184986A priority Critical patent/JP3782645B2/en
Publication of JP2002003986A publication Critical patent/JP2002003986A/en
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Publication of JP3782645B2 publication Critical patent/JP3782645B2/en
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Expired - Fee Related legal-status Critical Current

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Abstract

PROBLEM TO BE SOLVED: To provide high tensile steel for large heat input welding, having excellent toughness in a heat affected zone when welding at a heat input of >=200 kj/cm (e.g. as high as about 1,500 kj/cm). SOLUTION: The steel has a composition consisting of, by weight, 0.04-0.25% C, 0.02-0.5% Si, 0.2-2.0% Mn, <=0.02% pP, 0.002-0.02% S, 0.015-0.5% Al, 0.0005-0.005% Mg, proper amounts of one or more elements among Cu, Ni, Cr, Mo, Nb, V, Ti and B as selective elements, and the balance Fe with inevitable impurities and also has a structure containing (Mn, Mg)S of 0.005-0.5 μm particle size in proportions of 1.0×105 to 1.0×107 pieces per square mm. The growth of γ-grains in HAZ in very large heat input welding can be suppressed by the pinning action of the fine (Mn, Mg)S particles, and toughness in HAZ can be improved.

Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【発明の属する技術分野】本発明は高層建築等のボック
ス柱の組み立てで適用されるエレクトロスラグ溶接、あ
るいは、造船・橋梁等で適用されるエレクトロガス溶接
などの超大入熱溶接における熱影響部(以下、HAZと
称する)靭性に優れた溶接用高張力鋼に関するものであ
る。特に、入熱が200kJ/cm以上で、例えば75
0〜1500kJ/cm程度でも優れたHAZ靭性を有
するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a heat-affected zone in ultra-high heat input welding such as electroslag welding applied in assembling box columns of high-rise buildings or electrogas welding applied in ships and bridges. The present invention relates to a high-strength steel for welding having excellent toughness. Particularly, when the heat input is 200 kJ / cm or more, for example, 75 kJ / cm.
It has excellent HAZ toughness even at about 0 to 1500 kJ / cm.

【0002】[0002]

【従来の技術】最近の建築構造物の高層化に伴い、鋼製
柱が大型化し、これに使用される鋼材の板厚も増してき
た。このような大型の鋼製柱を溶接で組み立てる際に、
高能率で溶接することが必要であり、極厚鋼板を1パス
で溶接できるエレクトロスラグ溶接が広く適用されるよ
うになってきている。また、造船・橋梁分野においても
板厚が25mm程度以上の鋼板を1パスで溶接するエレ
クトロガス溶接が広く適用されるようになってきた。典
型的な入熱の範囲は200〜1500kJ/cmであ
り、このような超大入熱溶接ではサブマージアーク溶接
などの大入熱溶接(入熱は200kJ/cm未満)とは
異なり、溶接融合線(FL)付近やHAZが受ける熱履
歴において1350℃以上の高温滞留時間が極めて長く
なり(超大入熱溶接では大入熱溶接の数倍〜数十倍長時
間滞留する)、オーステナイト粒の粗大化が極めて顕著
であり、HAZの靭性を確保することが困難であった。
最近の大地震を契機として建築構造物の信頼性確保が急
務の課題であり、このような超大入熱溶接HAZ部の靭
性向上を達成することは極めて重要な課題である。
2. Description of the Related Art With the recent increase in the height of building structures, steel columns have become larger and the thickness of steel materials used for the columns has also increased. When assembling such large steel columns by welding,
It is necessary to perform welding with high efficiency, and electroslag welding, which can weld extremely thick steel plates in one pass, has been widely applied. Also, in the field of shipbuilding and bridges, electrogas welding in which a steel plate having a thickness of about 25 mm or more is welded in one pass has been widely applied. A typical heat input range is 200 to 1500 kJ / cm, and such a super large heat input welding differs from a large heat input welding such as a submerged arc welding (heat input is less than 200 kJ / cm) and a welding fusion wire (the heat input is less than 200 kJ / cm). In the thermal history near FL or HAZ, the high-temperature residence time of 1350 ° C. or more becomes extremely long (remains several to several tens of times longer in large heat input welding than in large heat input welding), and austenite grains become coarse. It was extremely remarkable, and it was difficult to secure the toughness of HAZ.
It is an urgent task to secure the reliability of building structures in the wake of the recent large earthquake, and it is extremely important to achieve such improvement in the toughness of the HAZ portion having a very large heat input weld.

【0003】従来から大入熱溶接HAZ部の靭性向上に
関しては以下に示すように多くの知見・技術があるが、
上記の通り、超大入熱溶接と大入熱溶接とではHAZが
受ける熱履歴、特に、1350℃以上における滞留時間
が大きく異なるために、大入熱溶接HAZ靭性向上技術
を単純に本発明の対象分野に適用することはできない。
[0003] Conventionally, there are many knowledge and techniques for improving the toughness of a high heat input welding HAZ as shown below.
As described above, since the heat history applied to the HAZ between the very large heat input welding and the large heat input welding, especially the residence time at 1350 ° C. or more, is greatly different, the technique for improving the large heat input welding HAZ toughness is simply applied to the present invention. It cannot be applied to the field.

【0004】従来の大入熱溶接HAZ靭性向上は大きく
分類すると主に二つの基本技術に基づいたものであっ
た。その一つは鋼中粒子によるピン止め効果を利用した
オーステナイト粒粗大化防止技術であり、他の一つはオ
ーステナイト粒内フェライト変態利用による有効結晶粒
微細化技術である。
[0004] The conventional high heat input welding HAZ toughness improvement is largely based on two basic technologies. One is a technique for preventing austenite grain coarsening using the pinning effect of particles in steel, and the other is an effective grain refinement technique using ferrite transformation in austenite grains.

【0005】「鉄と鋼」、第61年(1975)第11
号には、各種の鋼中窒化物・炭化物についてオーステナ
イト粒成長抑制効果を検討し、Tiを添加した鋼ではT
iNの微細粒子が鋼中に生成し、大入熱溶接HAZにお
けるオーステナイト粒成長を効果的に抑制する技術が開
示されている。
"Iron and Steel", 61th year (1975), eleventh
No. 3 examines the effect of suppressing austenite grain growth on various types of nitrides and carbides in steel.
There is disclosed a technique in which fine particles of iN are generated in steel to effectively suppress austenite grain growth in a large heat input welding HAZ.

【0006】特開昭60−184663号公報には、A
lを0.04〜0.10%、Tiを0.002〜0.0
2%、さらに、希土類元素(REM)を0.003〜
0.05%含有する鋼において、入熱が150kJ/c
mの大入熱溶接HAZ靭性を向上させる技術が開示され
ている。これは、REMが硫・酸化物を形成して大入熱
溶接時にHAZ部の粗粒化を防止する作用を有するため
である。
[0006] Japanese Patent Application Laid-Open No. 60-184663 discloses A
1 to 0.04 to 0.10%, Ti to 0.002 to 0.0
2%, rare earth element (REM) 0.003 to
Heat input of 150 kJ / c in steel containing 0.05%
A technique for improving the high heat input welding HAZ toughness of m is disclosed. This is because the REM has an action of forming sulfur / oxide and preventing the HAZ portion from coarsening during large heat input welding.

【0007】特開昭60−245768号公報には、粒
子径が0.1〜3.0μm、粒子数が5×103 〜1×
107 個/mm3 のTi酸化物、あるいはTi酸化物と
Ti窒化物との複合体のいずれかを含有する鋼では、入
熱が100kJ/cmの大入熱溶接HAZ内でこれら粒
子がフェライト変態核として作用することによりHAZ
組織が微細化してHAZ靭性を向上できる技術が開示さ
れている。
Japanese Patent Application Laid-Open No. 60-245768 discloses that the particle size is 0.1 to 3.0 μm and the number of particles is 5 × 10 3 to 1 ×.
In steels containing either 10 7 / mm 3 Ti oxide or a composite of Ti oxide and Ti nitride, these particles become ferrite in a large heat input welding HAZ with a heat input of 100 kJ / cm. HAZ by acting as a transformation nucleus
A technique capable of improving the HAZ toughness by refining the structure is disclosed.

【0008】特開平2−254118号公報には、Ti
とSを適量含有する鋼において大入熱溶接HAZ組織中
にTiNとMnSの複合析出物を核として粒内フェライ
トが生成し、HAZ組織を微細化することによりHAZ
靭性の向上が図れる技術が開示されている。
[0008] JP-A-2-254118 discloses that Ti
In a steel containing a proper amount of S and S, intragranular ferrite is formed in the large heat input welding HAZ structure by using a composite precipitate of TiN and MnS as a nucleus, and the HAZ structure is refined.
A technique capable of improving toughness is disclosed.

【0009】特開昭61−253344号公報には、A
lを0.005〜0.08%、Bを0.0003〜0.
0050%含み、さらに、Ti、Ca、REMのうち少
なくとも1種以上を0.03%以下含む鋼は大入熱溶接
HAZで未溶解のREM・Caの酸化・硫化物あるいは
TiNを起点として冷却過程でBNを形成し、これから
フェライトが生成することにより大入熱HAZ靭性が向
上する技術が開示されている。
Japanese Patent Application Laid-Open No. 61-253344 discloses A
1 is 0.005 to 0.08%, and B is 0.0003 to 0.
Steel containing at least 0050% and at least 0.03% of at least one of Ti, Ca and REM is subjected to a cooling process starting from unmelted REM / Ca oxide / sulfide or TiN in the large heat input welding HAZ. A technique is disclosed in which a high heat input HAZ toughness is improved by forming BN and forming ferrite from the BN.

【0010】特開平9−157787号公報には、Mg
含有酸化物を1平方mmあたり40,000〜100,
000個含み、且つ、粒子径が0.20〜5.0μmの
Ti含有酸化物とMnSからなる複合体を1平方mmあ
たり20〜400個含む鋼では、オーステナイト粒成長
抑制と粒内フェライト変態促進により超大入熱溶接HA
Z靭性を向上できる技術が開示されている。
Japanese Patent Application Laid-Open No. 9-157787 discloses that Mg
The content of oxides is 40,000 to 100,
Steel containing 20 to 400 per square mm of a composite comprising Ti-containing oxide and MnS having a particle diameter of 0.20 to 5.0 μm and suppressing austenite grain growth and promoting intragranular ferrite transformation is included. High heat input welding HA
A technique capable of improving the Z toughness is disclosed.

【0011】特開平11−286743号公報には、粒
子径が0.005〜0.5μmのMgO、MgS、Mg
(O、S)の2種以上を含む鋼では、これらの微細粒子
によるオーステナイト粒成長抑制により超大入熱溶接H
AZ靭性を向上できる技術が開示されている。
JP-A-11-286743 discloses that MgO, MgS, Mg having a particle size of 0.005 to 0.5 μm is used.
In steels containing two or more types of (O, S), ultra-high heat input welding H
A technique capable of improving AZ toughness is disclosed.

【0012】[0012]

【発明が解決しようとする課題】「鉄と鋼」、第61年
(1975)第11号に開示されている技術はTiNを
はじめとする窒化物を利用してオーステナイト粒成長抑
制を図るものであり、大入熱溶接では効果が発揮される
が、本発明が対象とする超大入熱溶接では1350℃以
上の滞留時間が極めて長いために、ほとんどのTiNは
固溶し、粒成長抑制の効果を失う。従って、この技術を
本発明が目的とする超大入熱溶接HAZの靭性には適用
できない。
The technique disclosed in "Iron and Steel", No. 11, 1986 (1975) aims at suppressing austenite grain growth by using nitrides such as TiN. Yes, the effect is exhibited in large heat input welding, but in the ultra-high heat input welding targeted by the present invention, since the residence time at 1350 ° C. or more is extremely long, most of TiN forms a solid solution, and the effect of suppressing grain growth is exhibited. Lose. Therefore, this technique cannot be applied to the toughness of the ultra-high heat input welding HAZ which is the object of the present invention.

【0013】特開昭60−184663号公報に開示さ
れた技術はREMの硫化・ 酸化物を利用して大入熱溶接
時にHAZ部の粗粒化を防止するものである。硫化・酸
化物は窒化物に比べて1350℃以上の高温における安
定性は高いので、粒成長抑制効果は維持される。しかし
ながら、硫・酸化物を微細に分散させることは困難であ
る。硫・酸化物の個数密度が低いために、個々の粒子の
ピン止め効果は維持されるとしても超大入熱溶接HAZ
のオーステナイト粒径を小さくすることには限度があ
り、これだけで靭性向上をはかることはできない。
The technique disclosed in Japanese Patent Application Laid-Open No. 60-184663 is to prevent the HAZ from coarsening during large heat input welding by using REM sulfide / oxide. Sulfurized oxide has a higher stability at a high temperature of 1350 ° C. or higher than nitride, so that the effect of suppressing grain growth is maintained. However, it is difficult to finely disperse sulfur oxides. Ultra-high heat input welding HAZ even though pinning effect of individual particles is maintained due to low number density of sulfur and oxide
There is a limit to reducing the austenite grain size of the steel, and it is not possible to improve the toughness by itself.

【0014】特開昭60−245768号公報に記載さ
れた技術はTi酸化物、あるいはTi酸化物とTi窒化
物との複合体のいずれかの粒子がフェライト変態核とし
て作用することによりHAZ組織を微細化させてHAZ
靭性を向上させるものであり、Ti酸化物の高温安定性
を考慮すると超大入熱溶接においてもその効果は維持さ
れる。しかしながら、粒内変態核から生成するフェライ
トの結晶方位は全くランダムというわけではなく、母相
オーステナイトの結晶方位の影響を受ける。従って、超
大入熱溶接でオーステナイト粒が粗大化する場合には粒
内変態だけでHAZ組織を微細化することには限度があ
る。
The technique described in Japanese Patent Application Laid-Open No. 60-245768 discloses that a HAZ structure is formed by particles of either Ti oxide or a composite of Ti oxide and Ti nitride acting as ferrite transformation nuclei. HAZ
It improves toughness, and its effect is maintained even in ultra-high heat input welding in consideration of the high temperature stability of Ti oxide. However, the crystal orientation of ferrite generated from the intragranular transformation nucleus is not completely random, and is affected by the crystal orientation of the parent phase austenite. Therefore, when austenite grains are coarsened by ultra-high heat input welding, there is a limit to reducing the HAZ structure only by intragranular transformation.

【0015】特開平2−254118号公報に開示され
た技術は、TiN−MnS複合析出物からフェライトを
変態させるものであり、大入熱溶接のように1350℃
以上の滞留時間が比較的短い場合には効果を発揮する
が、エレクトロスラグあるいはエレクトロガス溶接のよ
うな超大入熱溶接においては1350℃以上の滞留時間
が長く、この間に多くのTiNは固溶してしまうために
フェライト変態核が消失し、その効果が十分には発揮で
きない。
The technique disclosed in Japanese Patent Application Laid-Open No. 2-254118 is for transforming ferrite from a TiN—MnS composite precipitate, and is similar to large heat input welding at 1350 ° C.
The effect is exhibited when the above residence time is relatively short. However, in ultra-high heat input welding such as electroslag or electrogas welding, the residence time of 1350 ° C. or more is long, and during this time, a large amount of TiN forms a solid solution. As a result, the ferrite transformation nuclei disappear and the effect cannot be sufficiently exhibited.

【0016】特開昭61−253344号公報に開示さ
れた技術は、REM・Caの酸化・硫化物あるいはTi
N上にBNを形成し、これからフェライトを生成させる
ことによりHAZ組織を微細化するものであり、超大入
熱溶接においても同様な効果は期待できる。しかしなが
ら、REM・Caの酸化・硫化物の個数を増加させるこ
とは困難であり、しかもTiNは固溶してフェライト変
態だけでは超大入熱溶接HAZの靭性向上には限度があ
る。
The technique disclosed in Japanese Patent Application Laid-Open No. 61-253344 discloses an oxidation / sulfide of REM / Ca or Ti
BN is formed on N and ferrite is formed from the BN to refine the HAZ structure. Similar effects can be expected in ultra-high heat input welding. However, it is difficult to increase the number of oxides and sulfides of REM / Ca, and TiN forms a solid solution, and there is a limit in improving the toughness of ultra-high heat input welding HAZ only by ferrite transformation.

【0017】特開平9−157787号公報に開示され
た技術は本発明者らによるものであり、0.01〜0.
20μmの微細なMg含有酸化物によるオーステナイト
粒成長抑制と0.20〜5.0μmのTi含有酸化物と
MnSからなる複合体による粒内フェライト変態促進に
より超大入熱溶接HAZ靭性を向上できる。しかしなが
ら、Ti含有酸化物の生成にはAl量を0.005%以
下に抑制する必要があり、従来のAl添加鋼の利点を損
なう。すなわち、従来のAl量が0.010〜0.5%
程度のAl脱酸鋼においては、鋼中のAlによる酸化発
熱を利用することで溶鋼温度を容易に制御することがで
き、安価かつ安定な鋼の量産を可能にしてきた。Al添
加量を0.005%程度以下に制限すると、溶鋼加熱装
置による加熱等の、Alの酸化発熱による溶鋼温度制御
を代替する手段が必要となる。溶鋼中のAlは大気中の
酸素による溶鋼汚染防止の役割も有し、また、Alは窒
化物を形成することで材質確保に有効であることも広く
知られており、Al量の0.005%以下への低減はこ
れらのAl添加の利点を損なうことが課題として残る。
The technique disclosed in Japanese Patent Application Laid-Open No. 9-157787 has been developed by the present inventors, and is disclosed in Japanese Patent Application Laid-Open No. H09-157787.
The super large heat input welding HAZ toughness can be improved by suppressing the austenite grain growth by the 20 μm fine Mg-containing oxide and promoting the intragranular ferrite transformation by the composite of 0.20-5.0 μm Ti-containing oxide and MnS. However, in order to generate a Ti-containing oxide, it is necessary to suppress the Al content to 0.005% or less, which impairs the advantages of the conventional Al-added steel. That is, the conventional Al content is 0.010 to 0.5%
In a degree of Al deoxidized steel, the temperature of molten steel can be easily controlled by utilizing the heat generated by oxidation of Al in the steel, and low-cost and stable mass production of steel has been enabled. If the amount of Al added is limited to about 0.005% or less, a means for controlling the temperature of molten steel by heat generated by oxidation of Al, such as heating by a molten steel heating device, is required. It is widely known that Al in molten steel also has a role of preventing molten steel from being contaminated by oxygen in the atmosphere, and that Al is effective in securing the material by forming nitrides. The problem remains that the reduction to less than% impairs the advantages of these Al additions.

【0018】特開平11−286743号公報に開示さ
れた技術も本発明者らによるものであり、0.005〜
0.5μmのMgO、MgS、Mg(O、S)の2種以
上を含む鋼では、これらの微細粒子によるオーステナイ
ト粒成長抑制により超大入熱溶接HAZ靭性を向上でき
る。しかしながら、微細なMgOの生成にはAl量を
0.01%以下に抑制する必要があり、やはり、上述し
たAl添加の利点を損なうことが課題として残る。
The technique disclosed in Japanese Patent Application Laid-Open No. H11-286743 is also based on the present inventors, and is disclosed in US Pat.
In steel containing two or more of 0.5 μm of MgO, MgS, and Mg (O, S), the super large heat input welding HAZ toughness can be improved by suppressing austenite grain growth by these fine particles. However, in order to generate fine MgO, it is necessary to suppress the amount of Al to 0.01% or less, and the problem remains that the advantage of the above-described addition of Al is lost.

【0019】本発明は高層建築物のボックス柱の組み立
てで適用されるエレクトロスラグ溶接、造船・橋梁等で
適用されるエレクトロガス溶接などの入熱が200kJ
/cm以上の超大入熱溶接におけるHAZ靭性に優れた
溶接用高張力鋼をAl添加鋼を前提に提供することにあ
る。
The present invention has a heat input of 200 kJ such as electroslag welding applied in assembling box columns of a high-rise building and electrogas welding applied in shipbuilding and bridges.
Another object of the present invention is to provide a high-strength steel for welding having excellent HAZ toughness in ultra-high heat input welding of at least / cm or more on the premise of Al-added steel.

【0020】[0020]

【課題を解決するための手段】本発明者らは、超大入熱
溶接HAZの靭性向上にはHAZ組織の微細化が必須で
あり、これはHAZのオーステナイト粒成長を著しく抑
制することにより可能であること、さらに、Al添加鋼
を前提として、微細な(Mn,Mg)S粒子が1350
℃以上の高温で極めて安定であり、かつ微細分散が可能
であることを新規に知見した。この新規知見によりHA
Zのオーステナイト粒成長を著しく抑制し得ること、そ
の結果、超大入熱HAZ靭性を大きく向上できることを
知見して本発明を成した。
Means for Solving the Problems The inventors of the present invention have found that miniaturization of the HAZ structure is indispensable for improving the toughness of the ultra-high heat input welding HAZ, and this can be achieved by remarkably suppressing the austenite grain growth of the HAZ. In addition, assuming that Al-added steel, fine (Mn, Mg) S particles are 1350
It has been newly discovered that the composition is extremely stable at a high temperature of not less than ° C and that fine dispersion is possible. With this new finding, HA
The present invention has been made based on the finding that the austenite grain growth of Z can be remarkably suppressed, and as a result, the ultra-high heat input HAZ toughness can be greatly improved.

【0021】本発明の要旨は次の通りである。 (1)重量%で、0.04≦C≦0.25、0.02≦
Si≦0.5、0.2≦Mn≦2.0、P≦0.02、
0.002≦S≦0.02、0.015<Al≦0.
5、0.0005≦Mg≦0.005、を含有し、粒子
径が0.005〜0.5μmの(Mn,Mg)Sを1平
方mmあたり1.0×105 〜1.0×107 個含み、
残部Feおよび不可避的不純物よりなる鋼であることを
特徴とする超大入熱溶接用高張力鋼。 (2)更に母材強度上昇元素群を、重量%で、0.05
≦Cu≦1.5、0.05≦Ni≦2.0、0.02≦
Cr≦1.0、0.02≦Mo≦1.0、0.005≦
Nb≦0.05、0.005≦V≦0.1、0.005
≦Ti≦0.025、0.0004≦B≦0.004、
の1種または2種以上を含有することを特徴とする
(1)記載の超大入熱溶接用高張力鋼にある。
The gist of the present invention is as follows. (1) 0.04 ≦ C ≦ 0.25, 0.02 ≦
Si ≦ 0.5, 0.2 ≦ Mn ≦ 2.0, P ≦ 0.02,
0.002 ≦ S ≦ 0.02, 0.015 <Al ≦ 0.
5, (Mn, Mg) S containing 0.0005 ≦ Mg ≦ 0.005 and having a particle diameter of 0.005 to 0.5 μm per square mm of 1.0 × 10 5 to 1.0 × 10 5 Including seven ,
A high-strength steel for ultra-high heat input welding, characterized in that the steel is composed of a balance of Fe and unavoidable impurities. (2) Further, the group of elements for increasing the base metal strength is 0.05% by weight.
≦ Cu ≦ 1.5, 0.05 ≦ Ni ≦ 2.0, 0.02 ≦
Cr ≦ 1.0, 0.02 ≦ Mo ≦ 1.0, 0.005 ≦
Nb ≦ 0.05, 0.005 ≦ V ≦ 0.1, 0.005
≦ Ti ≦ 0.025, 0.0004 ≦ B ≦ 0.004,
(1) The high tensile strength steel for ultra-high heat input welding according to (1), characterized in that it contains one or more of the following.

【0022】また、本発明で言うところの「溶接用高張
力鋼」とは、例えば、JIS G3106「溶接構造用
圧延鋼材」、JIS G3115「圧力容器用鋼板」、
JIS G3118「中・常温圧力容器用炭素鋼鋼
板」、JIS G3124「中・常温圧力容器用高強度
鋼板」、JIS G3126「低温用圧力容器用炭素鋼
鋼板」、及び、JIS G3128「溶接構造用高降伏
点鋼板」に相当するものである。
The "high-strength steel for welding" referred to in the present invention includes, for example, JIS G3106 "Rolled steel material for welded structures", JIS G3115 "Steel for pressure vessels",
JIS G3118 “Carbon steel sheet for medium / normal temperature pressure vessel”, JIS G3124 “High strength steel sheet for medium / normal temperature pressure vessel”, JIS G3126 “Carbon steel sheet for low pressure pressure vessel”, and JIS G3128 “Height for welded structure” Yield point steel plate ".

【0023】[0023]

【発明の実施の形態】このような超大入熱溶接用高張力
鋼を、大量の製造実績があり優れた量産プロセスである
Al脱酸を前提に製造する。本発明者らは、超大入熱溶
接HAZの組織と靭性の関係に関する詳細な調査・研究
を実施した結果、従来の大入熱溶接HAZの組織制御ま
たは靭性向上法をそのまま適用しても、超大入熱溶接H
AZ靭性は限られたものであり、靭性向上にはHAZの
オーステナイト粒を著しく微細化する必要があるとの結
論に達した。
DESCRIPTION OF THE PREFERRED EMBODIMENTS Such a high-tensile steel for ultra-high heat input welding is manufactured on the premise of Al deoxidation, which is an excellent mass production process with a large production track record. The present inventors have conducted detailed investigations and studies on the relationship between the structure and toughness of the ultra-high heat input welding HAZ. Heat input welding H
AZ toughness was limited, and it was concluded that austenitic grains of HAZ had to be remarkably refined to improve toughness.

【0024】まず、オーステナイト粒の微細化には鋼中
粒子によるピン止め効果を利用することが有効である
が、窒化物の中で最も熱的に安定であるとされるTiN
でも1350℃以上に長時間加熱されるとほとんどが溶
解し、ピン止め効果を失うために、超大入熱溶接への適
用には限度がある。従って、高温で安定である粒子の利
用が必須となる。しかしながら、従来技術のREMある
いはCa酸化物(酸化・硫化物も含む)では、超大入熱
溶接HAZのオーステナイト粒粗大化抑制に十分な程度
にこれら酸化物を鋼中に微細分散させることは極めて困
難である。
First, it is effective to use the pinning effect of the particles in the steel to refine the austenite grains, but TiN is considered to be the most thermally stable among nitrides.
However, if it is heated to 1350 ° C. or more for a long time, most of it melts and loses the pinning effect, so that there is a limit to its application to ultra-high heat input welding. Therefore, the use of particles that are stable at high temperatures is essential. However, with conventional REM or Ca oxides (including oxides and sulfides), it is extremely difficult to finely disperse these oxides in steel to an extent sufficient to suppress austenite grain coarsening in ultra-high heat input welding HAZs. It is.

【0025】本発明者らは、これまでに各種の粒子につ
いて比較検討した結果、微細なMg含有酸化物が有効で
あることをすでに知見している。しかしながら、これら
の微細酸化物を鋼中に多量に生成させるには、鋼中のA
l量を例えば0.005%程度以下に抑制する必要があ
り、先に述べたようにAl添加の利点を損なう。
The inventors of the present invention have already found that fine Mg-containing oxides are effective as a result of comparative studies on various particles. However, in order to generate a large amount of these fine oxides in steel, A
It is necessary to suppress the l content to, for example, about 0.005% or less, which impairs the advantage of Al addition as described above.

【0026】本発明者らはAl脱酸鋼を前提に各種の粒
子について比較検討した結果、(Mn,Mg)S粒子が
高温で安定で、しかも微細分散に適した粒子であること
を新規に知見した。HAZのオーステナイト粒成長抑制
に効果を発揮する粒子は主に0.1μm以下のものであ
るが、Mn、Mg、S、Al添加量などを制御すること
により、微細な(Mn,Mg)Sを鋼中に多量に微細分
散させることが可能である。
The present inventors have conducted a comparative study on various particles based on the assumption that Al deoxidized steel is used. As a result, it has been newly found that (Mn, Mg) S particles are stable at high temperatures and suitable for fine dispersion. I learned. Particles that exhibit an effect of suppressing austenite grain growth of HAZ are mainly 0.1 μm or less, but fine (Mn, Mg) S can be produced by controlling the amounts of Mn, Mg, S, and Al added. It can be finely dispersed in a large amount in steel.

【0027】従来よりAl脱酸鋼には0.2〜2%程度
のMnおよび0.002〜0.02%程度のSは添加さ
れており、MnSを形成することは広く知られている。
このMnSは高温で不安定であり溶解してしまうため、
オーステナイト粒微細化粒子にはなり得なかった。しか
しながら、MnS中のMnのいくつかがMgに置き換わ
ったと考えられる(Mn,Mg)Sでは、MnSとはそ
の性質が全く異なり、高温で極めて安定であり、しかも
容易に微細分散することができる。(Mn,Mg)Sが
高温で安定でありしかも微細分散しやすい理由は現在の
所不明である。
Conventionally, Mn of about 0.2 to 2% and S of about 0.002 to 0.02% have been added to Al deoxidized steel, and it is widely known that MnS is formed.
Since this MnS is unstable at high temperature and is dissolved,
Austenitic grains could not be refined. However, (Mn, Mg) S, which is considered to have some of Mn in MnS replaced by Mg, is completely different from MnS in its properties, is extremely stable at high temperatures, and can be easily finely dispersed. The reason why (Mn, Mg) S is stable at high temperature and easily dispersed finely is unknown at present.

【0028】単に鋼中にMgを添加しただけでは(M
n,Mg)Sはほとんど生成しない。その理由はMgが
強脱酸元素であり酸化物となってしまうことにある。M
gは蒸気圧が高く、多量に添加しても溶鋼中に歩留りに
くい元素である。このため、0.0005〜0.005
%程度の微量のMgが酸化物として消費されてしまうの
を防ぎ、(Mn,Mg)Sを生成させることは極めて重
要となる。図1にMn、Mg、S添加量が本発明範囲内
の鋼における、0.005〜0.5μmの大きさの(M
n,Mg)S粒子の個数に及ぼすAl添加量の影響を示
す。Al添加量が0.015%未満では(Mn,Mg)
S粒子の個数は少ない。この時のMgは主にMgAl2
4 あるいはMgOとして酸化物として存在する。一
方、Al添加量が0.015%以上では、(Mn,M
g)S粒子の個数が顕著に増加し、酸化物はAl2 3
主体でMgの多くは(Mn,Mg)Sとして存在する。
すなわち、0.015%以上のAl添加により微細な
(Mn,Mg)S粒子を多数生成させることができる。
Simply adding Mg to steel (M
n, Mg) S is hardly formed. The reason is that Mg is a strong deoxidizing element and becomes an oxide. M
g is an element that has a high vapor pressure and is difficult to yield in molten steel even when added in a large amount. Therefore, 0.0005 to 0.005
It is extremely important to prevent a trace amount of Mg of about% from being consumed as an oxide and to generate (Mn, Mg) S. FIG. 1 shows (M) having a size of 0.005 to 0.5 μm in a steel in which the added amounts of Mn, Mg and S are within the range of the present invention.
The effect of the amount of Al added on the number of (n, Mg) S particles is shown. When the amount of Al added is less than 0.015%, (Mn, Mg)
The number of S particles is small. Mg at this time is mainly MgAl 2
It exists as an oxide as O 4 or MgO. On the other hand, when the amount of Al added is 0.015% or more, (Mn, M
g) The number of S particles is significantly increased, and the oxide is Al 2 O 3
Most of Mg mainly exists as (Mn, Mg) S.
That is, a large number of fine (Mn, Mg) S particles can be generated by adding 0.015% or more of Al.

【0029】本発明では、(Mn,Mg)Sの粒子径を
0.005〜0.5μmに限定した。0.005μm未
満ではオーステナイト粒成長抑制効果が小さくなる。ま
た、0.5μm超ではこれらの粒子や粒子と地鉄との界
面が破壊起点となる確率が高くなり靭性を低下させる。
0.005〜0.5μmのサイズの(Mn,Mg)S粒
子の個数が1平方mmあたり1.0×105 個以上の場
合にオーステナイト粒成長抑制効果が顕著となり、1.
0×107 個を超えると鋼の延性を低下させるので、
(Mn, Mg)S粒子の個数を1平方mmあたり1.0
×105 〜1.0×107 個に制限した。
In the present invention, the particle diameter of (Mn, Mg) S is limited to 0.005 to 0.5 μm. If the thickness is less than 0.005 μm, the effect of suppressing austenite grain growth becomes small. On the other hand, if it exceeds 0.5 μm, the probability that these particles or the interface between the particles and the base iron become fracture starting points increases, and the toughness decreases.
When the number of (Mn, Mg) S particles having a size of 0.005 to 0.5 μm is 1.0 × 10 5 or more per 1 mm 2, the effect of suppressing austenite grain growth becomes remarkable.
If it exceeds 0 × 10 7, the ductility of the steel will be reduced.
The number of (Mn, Mg) S particles is set to 1.0 per square mm.
× 10 5 to 1.0 × 10 7 .

【0030】粒子個数の測定方法は、鋼板から抽出レプ
リカを作成し、特性X線検出器(EDX)付きの透過型
電子顕微鏡(TEM)で、0.005〜0.5μmの大
きさの粒子個数を、少なくとも1000μm2 以上の面
積につき測定し、単位面積当たりの個数に換算する。例
えば、2万倍の倍率にて1視野を100mm×80mm
として観察した場合、1視野あたりの観察面積は20μ
2 であるから少なくとも50視野につき観察を行う。
この時の0.005〜0.5μmの粒子の個数が50視
野(1000μm2 )で200個であれば、粒子個数は
1平方mmあたり2×105 個と換算できる。
The number of particles is measured by preparing an extraction replica from a steel plate and measuring the number of particles having a size of 0.005 to 0.5 μm with a transmission electron microscope (TEM) equipped with a characteristic X-ray detector (EDX). Is measured for an area of at least 1000 μm 2 and converted to the number per unit area. For example, one field of view is 100 mm x 80 mm at a magnification of 20,000 times.
Observed area per visual field is 20μ
Observe at least 50 fields of view because of m 2 .
If the number of particles of 0.005 to 0.5 μm at this time is 200 in 50 visual fields (1000 μm 2 ), the number of particles can be converted to 2 × 10 5 per square mm.

【0031】次に、個数を測定した粒子のうち、(M
n,Mg)S粒子がどれだけ存在したかを測定するが、
粒子個数は最低でも100個以上、多い場合には100
00個以上となるため全粒子を逐一同定することは大変
な作業となる。このため、少なくとも50個以上の粒子
について下記の条件にて(Mn,Mg)Sを同定しその
存在割合を求め、先に求めた粒子個数に(Mn,Mg)
Sの存在割合をかけることで(Mn,Mg)Sの個数を
求める。例えば、上述した粒子個数、1平方mmあたり
2×105 個に対し、(Mn,Mg)Sの存在割合が9
0%であった場合には(Mn,Mg)Sの個数は1平方
mmあたり1.8×105 個であるとする。
Next, among the particles whose number was measured, (M
Measure how much n, Mg) S particles were present,
The number of particles should be at least 100 or more,
Since the number of particles is 00 or more, identifying all the particles one by one is a serious task. For this reason, (Mn, Mg) S was identified for at least 50 or more particles under the following conditions, and its abundance was determined.
The number of (Mn, Mg) S is obtained by multiplying the existence ratio of S. For example, for the number of particles described above and 2 × 10 5 per square mm, the existing ratio of (Mn, Mg) S is 9
If it is 0%, the number of (Mn, Mg) S is assumed to be 1.8 × 10 5 per square mm.

【0032】次に(Mn,Mg)Sの同定方法について
述べる。本発明では(Mn,Mg)S中のMnとMgの
割合を重量%で60%≦Mn≦95%、5%≦Mg≦4
0%に限定する。Mn、Mg以外の元素が検出されて
も、Mn、Mgを主体とする硫化物であれば本発明のオ
ーステナイト粒微細化効果を発揮するものと考えられ
る。また、粒子中から微量のOが検出される場合がある
が、SとOの割合が重量%にて95%≦Sであり、含ま
れているOが5%未満と微量であれば(Mn,Mg)S
であるとみなす。尚、SとOの割合が重量%にて95%
≦Sであり、含まれているOが5%未満であっても、粒
子が明らかにMnSとMgOの複合体であると同定でき
る場合には、(Mn,Mg)Sとはみなさない。Mnと
Mgの割合およびSとOの割合は、EDXにて定量して
求める。この定量時に使用する電子ビーム径は0.00
1〜0.02μm、TEM観察倍率は5万〜100万倍
とし、微細な(Mn, Mg)S粒子内の任意の位置を定
量する。
Next, a method for identifying (Mn, Mg) S will be described. In the present invention, the ratio of Mn and Mg in (Mn, Mg) S is 60% ≦ Mn ≦ 95% and 5% ≦ Mg ≦ 4 by weight%.
Limited to 0%. Even if an element other than Mn and Mg is detected, it is considered that a sulfide mainly composed of Mn and Mg exerts the austenite grain refinement effect of the present invention. In addition, a small amount of O may be detected in the particles. However, if the ratio of S and O is 95% ≦ S in weight% and the contained O is less than 5% (Mn , Mg) S
Is assumed to be. The ratio of S and O is 95% by weight.
If ≦ S and the particles are clearly identified as a complex of MnS and MgO, even if the contained O is less than 5%, they are not regarded as (Mn, Mg) S. The ratios of Mn and Mg and the ratios of S and O are determined quantitatively by EDX. The electron beam diameter used for this determination is 0.00
1 to 0.02 μm, the TEM observation magnification is 50,000 to 1,000,000 times, and an arbitrary position in fine (Mn, Mg) S particles is quantified.

【0033】鋼板から抽出レプリカを作成した場合に、
0.005〜0.5μmのサイズの(Mn,Mg)S以
外の析出物、例えばセメンタイトや合金炭窒化物などが
多数生成して(Mn,Mg)S粒子の個数を測定しにく
い場合には、1400℃にて60秒程度保持して(M
n,Mg)S以外の粒子を固溶させ、その後急冷してセ
メンタイトや合金炭窒化物が少ないサンプルを作成し、
これから抽出レプリカを作成すると良い。
When an extraction replica is made from a steel sheet,
When a large number of precipitates other than (Mn, Mg) S having a size of 0.005 to 0.5 μm, such as cementite and alloy carbonitride, are formed, and it is difficult to measure the number of (Mn, Mg) S particles, , Held at 1400 ° C for about 60 seconds (M
n, Mg) Solution of particles other than S, and then quenching to make a sample with less cementite and alloy carbonitride,
It is good to make an extraction replica from now on.

【0034】上記のようなサイズおよび個数の粒子を鋼
中に分散させるためには、Mn、Mg、S、およびAl
の含有量を下記のとおり限定することが望ましい。Mn
は(Mn,Mg)Sを構成する元素であるため本発明に
必須の元素である。Mnは0.2%以上添加することで
微細な(Mn,Mg)Sの多量分散が可能となるので
0.2%を下限とした。Mnが2.0%を超えると(M
n,Mg)Sが粗大化しやすくなりHAZ靭性向上効果
が小さくなるため2.0%を上限とした。
In order to disperse particles having the above-mentioned size and number in steel, Mn, Mg, S, and Al
Is desirably limited as follows. Mn
Is an element constituting (Mn, Mg) S and is an essential element in the present invention. When Mn is added in an amount of 0.2% or more, a large amount of fine (Mn, Mg) S can be dispersed, so the lower limit is made 0.2%. When Mn exceeds 2.0% (M
Since (n, Mg) S tends to become coarse and the effect of improving the HAZ toughness is reduced, the upper limit is set to 2.0%.

【0035】Mgは(Mn,Mg)Sの生成に必須の元
素である。0.0005%未満では必要な個数の(M
n,Mg)S粒子を得ることはできない。より多量の微
細な(Mn,Mg)S粒子を生成させるためには0.0
015%以上の添加がより好ましい。0.005%超の
添加はMgが酸化物を生成するため(Mn,Mg)S量
が飽和しHAZ靭性向上効果も飽和する上、経済性を損
なうのでその上限値を0.005%とした。
Mg is an element essential for producing (Mn, Mg) S. If it is less than 0.0005%, the required number of (M
n, Mg) S particles cannot be obtained. In order to generate a larger amount of fine (Mn, Mg) S particles, 0.0
Addition of 015% or more is more preferable. If the addition exceeds 0.005%, Mg forms an oxide, so that the amount of (Mn, Mg) S is saturated, the effect of improving the HAZ toughness is saturated, and the economy is impaired. Therefore, the upper limit is made 0.005%. .

【0036】Sは(Mn,Mg)Sを生成させるために
必須の元素である。0.002%未満では(Mn,M
g)Sの量が不十分であるので、下限を0.002%と
した。より多量の微細な(Mn,Mg)S粒子を生成さ
せるためには0.003%以上の添加がより好ましい。
0.02%超含有すると、粗大な(Mn,Mg)Sが生
成して超大入熱溶接HAZのγ粒細粒化効果が得られな
いため上限値を0.02%とした。
S is an essential element for producing (Mn, Mg) S. If less than 0.002%, (Mn, M
g) Since the amount of S is insufficient, the lower limit was made 0.002%. In order to generate a larger amount of fine (Mn, Mg) S particles, 0.003% or more is more preferable.
If the content exceeds 0.02%, coarse (Mn, Mg) S is generated and the effect of refining the γ grains of the ultra-high heat input welding HAZ cannot be obtained, so the upper limit is set to 0.02%.

【0037】AlはMgが酸化物を生成することを抑制
し、Mgが(Mn,Mg)Sを生成するために必須の元
素であり、0.015%以上の添加が必要である。より
多量の微細な(Mn,Mg)S粒子を生成させるために
は、0.02%以上のAl添加がより好ましい。0.5
%を超えて含有すると、固溶AlによるHAZ脆化が起
るため(Mn,Mg)SによってHAZのオーステナイ
ト粒を微細化しても大きな靭性向上効果が得られない。
従って、上限を0.5%とした。
Al suppresses the formation of oxides by Mg, and Mg is an essential element for forming (Mn, Mg) S, and it is necessary to add 0.015% or more. In order to generate a larger amount of fine (Mn, Mg) S particles, Al addition of 0.02% or more is more preferable. 0.5
%, HAZ embrittlement due to solid-solution Al occurs, so that even if the austenitic grains of HAZ are refined by (Mn, Mg) S, a large effect of improving toughness cannot be obtained.
Therefore, the upper limit is set to 0.5%.

【0038】HAZ靭性はオーステナイト粒微細化と粒
内組織微細化だけではなく、合金元素により大きく変化
する。また、母材の強度確保のためにも適正な合金元素
を含有させる場合があるので、以下の理由により合金元
素の添加量を限定した。
The HAZ toughness varies not only with the refinement of austenite grains and with the refinement of the intragranular structure, but also with the alloy elements. Further, since an appropriate alloy element may be contained in order to secure the strength of the base material, the amount of the alloy element added is limited for the following reasons.

【0039】Cは母材の強度を上昇できる元素である。
0.04%未満では母材強度の確保が得られないので
0.04%を下限とした。逆に、Cを多く含有すると、
脆性破壊の起点となるセメンタイトや島状マルテンサイ
トを増加させるため、(Mn,Mg)SによってHAZ
のオーステナイト粒を微細化しても大きな靭性向上効果
が得られない。0.25%を超えると靭性低下が顕著と
なるので、これを上限値とした。
C is an element capable of increasing the strength of the base material.
If it is less than 0.04%, the base material strength cannot be secured, so 0.04% was made the lower limit. Conversely, if a large amount of C is contained,
In order to increase cementite and island-like martensite which are the starting points of brittle fracture, HAZ is formed by (Mn, Mg) S.
However, even if the austenite grains are refined, a large toughness improving effect cannot be obtained. If it exceeds 0.25%, the toughness is significantly reduced.

【0040】Siは母材強度上昇に有効な元素である。
0.02%未満ではこの効果が得られないので下限値を
0.02%とした。逆に、0.5%超含有すると、HA
Z組織中に島状マルテンサイトが多量に生成し、さら
に、フェライト地を硬化させるので、(Mn,Mg)S
によってHAZのオーステナイト粒を微細化しても大き
な靭性向上効果が得られない。従って、上限を0.5%
とした。
Si is an element effective for increasing the strength of the base material.
If less than 0.02%, this effect cannot be obtained, so the lower limit is set to 0.02%. Conversely, if the content exceeds 0.5%, HA
Since a large amount of island martensite is generated in the Z structure and hardens the ferrite ground, (Mn, Mg) S
Therefore, even if the austenite grains of the HAZ are made fine, a large toughness improving effect cannot be obtained. Therefore, the upper limit is 0.5%
And

【0041】Pは粒界脆化をもたらし、靭性に有害な元
素であり、低いほうが望ましい。0.02%超含有する
と(Mn,Mg)SによってHAZのオーステナイト粒
を微細化しても靭性低下が顕著となるので0.02%を
上限とする。
P is an element that causes grain boundary embrittlement and is harmful to toughness. If the content exceeds 0.02%, even if the austenite grains of the HAZ are refined by (Mn, Mg) S, the reduction in toughness becomes remarkable, so the upper limit is made 0.02%.

【0042】さらに、母材強度上昇に効果のある選択元
素の限定範囲を以下の理由で決定した。Cuは母材強度
上昇に有効な元素であり、特に、時効熱処理により微細
Cu相を析出させることにより著しい強度上昇が得られ
る。0.05%未満では強度上昇が得られないので、
0.05%を下限値とした。逆に、1.5%超含有する
と母材やHAZの脆化が顕著となるので上限値を1.5
%とした。
Further, the limited range of the selected element effective for increasing the base material strength was determined for the following reason. Cu is an element effective in increasing the strength of the base material. In particular, a remarkable increase in strength can be obtained by precipitating a fine Cu phase by aging heat treatment. If it is less than 0.05%, the strength cannot be increased,
0.05% was made the lower limit. Conversely, if the content exceeds 1.5%, the embrittlement of the base material and HAZ becomes remarkable, so the upper limit value is set to 1.5.
%.

【0043】Niは焼入れ性を上昇させることにより母
材強度上昇に効果を有し、さらに、靭性を向上させる。
0.05%未満ではこれらの効果が得られないので下限
値を0.05%とした。Niは高価な元素であり、2.
0%超含有すると経済性を損なうため上限値を2.0%
とした。
Ni has the effect of increasing the strength of the base metal by increasing the hardenability, and further improves the toughness.
If the content is less than 0.05%, these effects cannot be obtained, so the lower limit is set to 0.05%. Ni is an expensive element;
If the content exceeds 0%, the economical efficiency is impaired, so the upper limit is 2.0%.
And

【0044】Crは母材強度上昇に効果を有する。0.
02%未満ではこの効果が得られないので下限値を0.
02%とした。逆に、1.0%超含有するとHAZに硬
化組織を生成し、(Mn,Mg)SによってHAZのオ
ーステナイト粒を微細化しても大きなHAZ靭性向上効
果が得られない。従って、上限値を1.0%とした。
Cr is effective in increasing the strength of the base material. 0.
If it is less than 02%, this effect cannot be obtained, so the lower limit is set to 0.
02%. Conversely, if the content exceeds 1.0%, a hardened structure is formed in the HAZ, and even if the austenite grains of the HAZ are refined by (Mn, Mg) S, a large HAZ toughness improving effect cannot be obtained. Therefore, the upper limit was set to 1.0%.

【0045】Moは母材強度上昇に効果を有する。0.
02%未満ではこの効果が得られないので下限値を0.
02%とした。逆に、1.0%超含有するとHAZに硬
化組織を生成し、(Mn,Mg)SによってHAZのオ
ーステナイト粒を微細化しても大きなHAZ靭性向上効
果が得られない。従って、上限値を1.0%とした。
Mo is effective in increasing the strength of the base material. 0.
If it is less than 02%, this effect cannot be obtained, so the lower limit is set to 0.
02%. Conversely, if the content exceeds 1.0%, a hardened structure is formed in the HAZ, and even if the austenite grains of the HAZ are refined by (Mn, Mg) S, a large HAZ toughness improving effect cannot be obtained. Therefore, the upper limit was set to 1.0%.

【0046】Nbは母材の強度上昇および細粒化に有効
な元素である。0.005%未満ではこれらの効果が得
られないので下限値を0.005%とした。逆に、0.
05%超含有するとHAZにおけるNb炭窒化物の析出
が顕著となり、(Mn,Mg)SによってHAZのオー
ステナイト粒を微細化しても大きなHAZ靭性向上効果
が得られない。従って、上限値を0.05%とした。
Nb is an element effective for increasing the strength and refining the base material. If the content is less than 0.005%, these effects cannot be obtained, so the lower limit is set to 0.005%. Conversely, 0.
If the content exceeds 0.05%, precipitation of Nb carbonitride in the HAZ becomes remarkable, and even if the austenite grains of the HAZ are refined by (Mn, Mg) S, a large effect of improving the HAZ toughness cannot be obtained. Therefore, the upper limit is set to 0.05%.

【0047】Vは母材の強度上昇および細粒化に有効な
元素である。0.005%未満ではこれらの効果が得ら
れないので下限値を0.005%とした。逆に、0.1
%超含有するとHAZにおける炭窒化物の析出が顕著と
なり、(Mn,Mg)SによってHAZのオーステナイ
ト粒を微細化しても大きなHAZ靭性向上効果が得られ
ない。従って、上限値を0.1%とした。
V is an element effective for increasing the strength and refining the base material. If the content is less than 0.005%, these effects cannot be obtained, so the lower limit is set to 0.005%. Conversely, 0.1
%, The precipitation of carbonitrides in the HAZ becomes remarkable, and even if the austenite grains of the HAZ are refined by (Mn, Mg) S, a large effect of improving the HAZ toughness cannot be obtained. Therefore, the upper limit is set to 0.1%.

【0048】Tiは母材の強度上昇および細粒化に有効
な元素である。0.005%未満ではこれらの効果が得
られないので下限値を0.005%とした。逆に、0.
025%超含有すると粗大なTiNを生成しこれが破壊
の発生起点となるため、(Mn, Mg)SによってHA
Zのオーステナイト粒を微細化しても大きなHAZ靭性
向上効果が得られない。従って、上限値を0.025%
とした。
Ti is an element effective for increasing the strength and reducing the grain size of the base material. If the content is less than 0.005%, these effects cannot be obtained, so the lower limit is set to 0.005%. Conversely, 0.
If the content exceeds 025%, coarse TiN is generated and this becomes a starting point of the destruction, so that HA is formed by (Mn, Mg) S.
Even if the austenite grains of Z are refined, a large HAZ toughness improving effect cannot be obtained. Therefore, the upper limit is set to 0.025%
And

【0049】Bは制御冷却および焼入れ熱処理を施す場
合に特に顕著な強度上昇の効果を発揮する。0.000
4%未満の含有量では強度上昇効果が得られないので下
限値を0.0004%とした。逆に、0.004%超含
有すると粗大なB窒化物や炭硼化物を析出してこれが破
壊の起点となるために、(Mn, Mg)SによってHA
Zのオーステナイト粒を微細化しても大きなHAZ靭性
向上効果が得られない。従って、上限値を0.004%
とした。
B exerts a particularly remarkable increase in strength when subjected to controlled cooling and quenching heat treatment. 0.000
If the content is less than 4%, the effect of increasing the strength cannot be obtained, so the lower limit was made 0.0004%. Conversely, if the content exceeds 0.004%, coarse B nitrides and carbides are precipitated and serve as starting points of destruction.
Even if the austenite grains of Z are refined, a large HAZ toughness improving effect cannot be obtained. Therefore, the upper limit is 0.004%
And

【0050】本発明では微細な(Mn, Mg)Sを生成
させることが必要であり、このためにMn、Mg以外の
硫化物形成元素は極力下げることが望ましい。代表的な
元素はCaおよびREMであり、これらは0.0005
%以下とすることが望ましい。
In the present invention, it is necessary to generate fine (Mn, Mg) S. For this reason, it is desirable to reduce sulfide-forming elements other than Mn and Mg as much as possible. Representative elements are Ca and REM, which are 0.0005
% Is desirable.

【0051】本発明では鋼中酸素量については特に制限
しない。0.015〜0.5%のAl添加鋼では鋼中酸
素量は0.0003〜0.0040%程度となるが、こ
の範囲内の酸素量であれば本発明の細粒化効果を損なう
ことはない。本発明では鋼中窒素量については特に制限
しない。通常の0.0010〜0.010%程度の窒素
量であれば本発明の細粒化効果を損なうことはない。本
発明によるHAZ靭性向上効果は超大入熱溶接ばかりで
なく、大入熱溶接(例えば、100〜200未満kJ/
cm程度)でも有効である。なお、本発明では鋼中に通
常不可避的に含有される不純物元素は許容できる。C
u、Ni、Cr、Mo、Nb、V、B、N、Ti等が不
純物として混入しても本発明の性質を損なうことはな
い。例えば、Cu、Niは0.05%未満、Cr、およ
びMoは0.02%未満、Nb、V、Tiは0.005
%未満、Bは0.0004%未満まで不純物として含有
されていても特に悪影響を及ぼさない。
In the present invention, the oxygen content in steel is not particularly limited. In the case of the Al-added steel of 0.015 to 0.5%, the oxygen content in the steel is about 0.0003 to 0.0040%. However, if the oxygen content is within this range, the grain refining effect of the present invention is impaired. There is no. In the present invention, the amount of nitrogen in steel is not particularly limited. If the amount of nitrogen is about 0.0010 to 0.010% of the normal amount, the effect of the present invention on grain refinement is not impaired. The effect of improving the HAZ toughness according to the present invention is not only super large heat input welding but also large heat input welding (for example, 100 to less than 200 kJ /
cm) is also effective. In the present invention, impurity elements usually inevitably contained in steel are acceptable. C
Even if u, Ni, Cr, Mo, Nb, V, B, N, Ti and the like are mixed as impurities, the properties of the present invention are not impaired. For example, Cu and Ni are less than 0.05%, Cr and Mo are less than 0.02%, Nb, V, and Ti are 0.005%.
%, And B does not adversely affect even if it is contained as an impurity up to less than 0.0004%.

【0052】鋼の溶製方法は、例えば溶鋼温度を165
0℃以下として、溶鋼O濃度を0.01%以下、溶鋼S
濃度を0.02%以下とした状態で、適量のMn、M
g、およびAlを添加することにより溶鋼中に微細な
(Mn, Mg)Sを生成できる。この溶鋼を連続鋳造に
より鋳造することにより鋼中に(Mn, Mg)Sの微細
粒子を含有させることができる。鋼の製造方法は、(M
n, Mg)Sが所定量存在すれば良いので、鋳造後の加
熱、圧延、熱処理条件は母鋼材の機械的性質に応じて適
宜選定すればよい。
The method of smelting steel includes, for example, setting the temperature of molten steel to 165.
0 ° C or less, molten steel O concentration 0.01% or less, molten steel S
With the concentration set to 0.02% or less, appropriate amounts of Mn and M
By adding g and Al, fine (Mn, Mg) S can be generated in the molten steel. By casting the molten steel by continuous casting, fine particles of (Mn, Mg) S can be contained in the steel. The steel production method is (M
Since it is sufficient that a predetermined amount of (n, Mg) S is present, heating, rolling and heat treatment conditions after casting may be appropriately selected according to the mechanical properties of the base steel material.

【0053】[0053]

【実施例】以下に本発明の実施例を示す。転炉により鋼
を溶製し、連続鋳造により厚さが240〜400mmの
スラブを製造した。表1に鋼材の化学成分を示す。HA
Z靭性は鋼材の炭素等量にも大きく依存するので、本発
明の効果を確認するために、ほぼ同一の化学成分でM
n、Mg、S、Alのみを変えた鋼を溶製して比較し
た。
Examples of the present invention will be described below. Steel was melted by a converter, and a slab having a thickness of 240 to 400 mm was manufactured by continuous casting. Table 1 shows the chemical components of the steel materials. HA
Since the Z toughness greatly depends on the carbon equivalent of steel, in order to confirm the effect of the present invention, M
Steels in which only n, Mg, S, and Al were changed were melted and compared.

【0054】表2に鋼板の製造方法と板厚、母材の機械
的性質を示す。同表に示すとおり、制御圧延・制御冷却
法、焼入れ・焼戻し法、直接焼入れ・焼戻し法、および
直接焼入れ・二相域熱処理・焼戻し法により鋼板を製造
した。板厚は40〜100mmとした。図2に示すエレ
クトロガス溶接及び図3に示すエレクトロスラグ溶接に
より溶接試験体を作成した。板厚を35mmにそろえ
て、入熱が310kJ/cmのエレクトロガス溶接を実
施した。ここで、溶接の電流を610A、電圧を35
V、速度を4.1cm/分とした。同図に示すように、
溶接融合線(FL)および溶接融合線から3mm(HA
Z3)の位置がノッチ位置に一致するようにシャルピー
衝撃試験片を採取した。また、エレクトロスラグ溶接の
電流は380A、電圧は46V、速度は1.14cm/
分とした。入熱は920kJ/cmである。エレクトロ
スラグ溶接と同じノッチ位置となるようにシャルピー衝
撃試験片を採取した。衝撃試験は−5℃で行い、3本繰
り返しの平均値で靭性を評価した。結果を表3に示す。
また、エレクトロスラグ溶接部FL直近のHAZのミク
ロ組織観察を実施しγ粒径を測定し、さらに、0.00
5〜0.5μmの粒子径の(Mn, Mg)Sの粒子個数
を上記の方法に従って測定した結果を表3に併せて示
す。
Table 2 shows the steel sheet manufacturing method, the sheet thickness, and the mechanical properties of the base material. As shown in the table, steel sheets were produced by a controlled rolling / controlled cooling method, a quenching / tempering method, a direct quenching / tempering method, and a direct quenching / two-phase region heat treatment / tempering method. The plate thickness was 40 to 100 mm. Weld specimens were prepared by electrogas welding shown in FIG. 2 and electroslag welding shown in FIG. The plate thickness was adjusted to 35 mm, and electrogas welding with a heat input of 310 kJ / cm was performed. Here, the welding current was 610 A and the voltage was 35.
V, the speed was 4.1 cm / min. As shown in the figure,
3mm from welding fusion line (FL) and welding fusion line (HA
A Charpy impact test piece was collected so that the position of Z3) coincided with the notch position. The current of the electroslag welding was 380 A, the voltage was 46 V, and the speed was 1.14 cm /.
Minutes. The heat input is 920 kJ / cm. A Charpy impact test specimen was collected so as to be at the same notch position as in electroslag welding. The impact test was performed at −5 ° C., and the toughness was evaluated by the average value of three repetitions. Table 3 shows the results.
In addition, the microstructure of the HAZ near the electroslag weld FL was observed to measure the γ particle size, and further, 0.00
Table 3 also shows the results obtained by measuring the number of (Mn, Mg) S particles having a particle diameter of 5 to 0.5 μm according to the above method.

【0055】表3から明らかなとおり、本発明鋼は(M
n, Mg)Sの粒子個数が多く、エレクトロスラグ溶接
HAZのγ粒径が小さい。その結果、超大入熱溶接HA
Zの靭性が高い。同様に、エレクトロガス溶接でも本発
明鋼のHAZ靭性向上が明らかである。これに対して、
比較鋼9、10、18、20、24、26、28ではM
n、S、Al添加量は適正であるもののMg添加量が本
発明範囲より低いため(Mn, Mg)S粒子の個数が少
なくγ粒成長抑制効果は小さくHAZ靭性向上効果は小
さい。比較鋼5、16、22ではMn、Mg、Al添加
量は適正であるもののS添加量が本発明範囲より低いた
め(Mn, Mg)S粒子の個数が少なくγ粒成長抑制効
果は小さくHAZ靭性向上効果は小さい。比較鋼6では
S添加量が本発明範囲より高いため微細な(Mn, M
g)S粒子の個数が少なくγ粒成長抑制効果は小さくH
AZ靭性向上効果は小さい。比較鋼7、8ではMn、M
g、S添加量は適正であるもののAl添加量が本発明範
囲より低いため(Mn, Mg)S粒子の個数が少なくγ
粒成長抑制効果は小さくHAZ靭性向上効果は小さい。
比較鋼15ではMg、S、Al添加量は適正であるもの
のMn添加量が本発明範囲より低いため(Mn, Mg)
S粒子の個数が少なくγ粒成長抑制効果は小さくHAZ
靭性向上効果は小さい。
As is evident from Table 3, the steel of the present invention (M
The number of particles of n, Mg) S is large, and the γ particle size of the electroslag welding HAZ is small. As a result, very large heat input welding HA
Z has high toughness. Similarly, the improvement of the HAZ toughness of the steel of the present invention is evident also by electrogas welding. On the contrary,
For comparative steels 9, 10, 18, 20, 24, 26, 28, M
Although the addition amounts of n, S, and Al are appropriate, the addition amount of Mg is lower than the range of the present invention, so that the number of (Mn, Mg) S particles is small, the effect of suppressing γ grain growth is small, and the effect of improving HAZ toughness is small. In Comparative Steels 5, 16, and 22, the addition amounts of Mn, Mg, and Al are appropriate, but the addition amount of S is lower than the range of the present invention. The improvement effect is small. In Comparative Steel 6, since the amount of S added is higher than the range of the present invention, fine (Mn, M
g) The number of S particles is small and the effect of suppressing the
The effect of improving AZ toughness is small. In comparative steels 7 and 8, Mn, M
Although the amounts of g and S are appropriate, the number of (Mn, Mg) S particles is small because the amount of Al added is lower than the range of the present invention.
The effect of suppressing grain growth is small and the effect of improving HAZ toughness is small.
In Comparative Steel 15, although the added amounts of Mg, S, and Al were appropriate, the added amount of Mn was lower than the range of the present invention, so that (Mn, Mg)
The number of S particles is small and the effect of suppressing the growth of γ grains is small, and HAZ
The effect of improving toughness is small.

【0056】[0056]

【表1】 [Table 1]

【0057】[0057]

【表2】 [Table 2]

【0058】[0058]

【表3】 [Table 3]

【0059】[0059]

【発明の効果】以上説明したとおり、本発明鋼ではAl
脱酸鋼において鋼中に(Mn, Mg)Sの粒子を微細分
散させることにより入熱が200kJ/cm以上の超大
入熱溶接のFL及びHAZのγ粒成長抑制作用によりH
AZの有効結晶粒が微細化され、HAZ靭性を顕著に向
上させることができ、本発明を超大入熱溶接が適用され
る構造物に適用することにより、極めて信頼性の高い溶
接構造物を製造することが可能である。従って、本発明
は工業上極めて効果が大きい。
As described above, in the steel of the present invention, Al
Fine particles of (Mn, Mg) S are dispersed in steel in deoxidized steel so that the heat input is 200 kJ / cm or more.
Effective crystal grains of AZ are refined, HAZ toughness can be remarkably improved, and by applying the present invention to a structure to which ultra-high heat input welding is applied, a highly reliable welded structure is manufactured. It is possible to Therefore, the present invention is extremely effective industrially.

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

【図1】0.005〜0.5μmの大きさの(Mn, M
g)S粒子の個数に及ぼすAl添加量の影響を示す図で
ある。
FIG. 1: (Mn, M) with a size of 0.005 to 0.5 μm
g) is a diagram showing the effect of the amount of Al added on the number of S particles.

【図2】エレクトロガス溶接の条件を示す図である。FIG. 2 is a diagram showing conditions of electrogas welding.

【図3】エレクトロスラグ溶接の条件を示す図である。FIG. 3 is a diagram showing conditions of electroslag welding.

【符号の説明】[Explanation of symbols]

1 シャルピー試験片 2 シャルピー試験片のノッチ位置 : FL 3 シャルピー試験片のノッチ位置 : HAZ3mm 1 Charpy test piece 2 Notch position of Charpy test piece: FL 3 Notch position of Charpy test piece: HAZ 3 mm

───────────────────────────────────────────────────── フロントページの続き (72)発明者 植森 龍治 千葉県富津市新富20−1 新日本製鐵株式 会社技術開発本部内 (72)発明者 長尾 年道 愛知県東海市東海町5−3 新日本製鐵株 式会社名古屋製鐵所内 ──────────────────────────────────────────────────続 き Continuing on the front page (72) Inventor Ryuji Uemori 20-1 Shintomi, Futtsu-shi, Chiba Nippon Steel Corporation Technology Development Division (72) Inventor Tomoo Nagao 5-3 Tokai-cho, Tokai-shi, Aichi Nippon Steel Corporation Nagoya Works

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】 重量%で、0.04≦C≦0.25、
0.02≦Si≦0.5、0.2≦Mn≦2.0、P≦
0.02、0.002≦S≦0.02、0.015<A
l≦0.5、0.0005≦Mg≦0.005、を含有
し、粒子径が0.005〜0.5μmの(Mn,Mg)
Sを1平方mmあたり1.0×105 〜1.0×107
個含み、残部Feおよび不可避的不純物よりなる鋼であ
ることを特徴とする超大入熱溶接用高張力鋼。
(1) 0.04 ≦ C ≦ 0.25 by weight,
0.02 ≦ Si ≦ 0.5, 0.2 ≦ Mn ≦ 2.0, P ≦
0.02, 0.002 ≦ S ≦ 0.02, 0.015 <A
(Mn, Mg) containing l ≦ 0.5, 0.0005 ≦ Mg ≦ 0.005, and having a particle size of 0.005 to 0.5 μm.
S is set to 1.0 × 10 5 to 1.0 × 10 7 per 1 mm 2.
A high-strength steel for ultra-high heat input welding, characterized in that it is a steel containing, in balance, Fe and unavoidable impurities.
【請求項2】 更に母材強度上昇元素群を、重量%で、
0.05≦Cu≦1.5、0.05≦Ni≦2.0、
0.02≦Cr≦1.0、0.02≦Mo≦1.0、
0.005≦Nb≦0.05、0.005≦V≦0.
1、0.005≦Ti≦0.025、0.0004≦B
≦0.004、の1種または2種以上を含有することを
特徴とする請求項1記載の超大入熱溶接用高張力鋼。
2. The method of claim 1, further comprising:
0.05 ≦ Cu ≦ 1.5, 0.05 ≦ Ni ≦ 2.0,
0.02 ≦ Cr ≦ 1.0, 0.02 ≦ Mo ≦ 1.0,
0.005 ≦ Nb ≦ 0.05, 0.005 ≦ V ≦ 0.
1, 0.005 ≦ Ti ≦ 0.025, 0.0004 ≦ B
The high-strength steel for ultra-high heat input welding according to claim 1, comprising one or more of ≦ 0.004.
JP2000184986A 2000-06-20 2000-06-20 High strength steel for super large heat input welding Expired - Fee Related JP3782645B2 (en)

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