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JP4332064B2 - High HAZ toughness steel for high heat input welding with heat input of 20-100 kJ / mm - Google Patents
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JP4332064B2 - High HAZ toughness steel for high heat input welding with heat input of 20-100 kJ / mm - Google Patents

High HAZ toughness steel for high heat input welding with heat input of 20-100 kJ / mm Download PDF

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JP4332064B2
JP4332064B2 JP2004138064A JP2004138064A JP4332064B2 JP 4332064 B2 JP4332064 B2 JP 4332064B2 JP 2004138064 A JP2004138064 A JP 2004138064A JP 2004138064 A JP2004138064 A JP 2004138064A JP 4332064 B2 JP4332064 B2 JP 4332064B2
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実 伊藤
明彦 児島
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Nippon Steel Corp
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Description

本発明は、船舶、海洋構造物、中高層ビル、橋梁などに使用される溶接熱影響部(以下、HAZと称す。)の靭性に優れた溶接構造用鋼材に関するものである。   The present invention relates to a steel material for welded structure excellent in the toughness of a weld heat affected zone (hereinafter referred to as HAZ) used for ships, offshore structures, mid-to-high-rise buildings, bridges and the like.

近年、船舶、海洋構造物、中高層ビル、橋梁などの大型構造物に使用される溶接用鋼材の材質特性に対する要望は厳しさを増している。さらに、そのような構造物を建造する際、溶接の効率化を促進するため、エレクトロガス溶接法、エレクトロスラグ溶接法などに代表されるような大入熱溶接法の適用が希望されており、鋼材自身の靭性と同様に、HAZの靭性への要求も厳しさを増している。   In recent years, demands for material properties of steel materials for welding used in large structures such as ships, offshore structures, high-rise buildings, and bridges have increased. Furthermore, when building such a structure, in order to promote the efficiency of welding, it is desired to apply a high heat input welding method represented by an electrogas welding method, an electroslag welding method, Similar to the toughness of the steel itself, the demands on the toughness of the HAZ are becoming stricter.

従来から、大入熱溶接法が適用される鋼材のHAZ靭性に注目した提案は、数多くなされてきた。例えば、特許文献1等に開示されるように、微細なTi窒化物を鋼中に確保することによって、HAZのオーステナイト粒を小さくし、靭性を向上させる方法がある。また、特許文献2ではTi窒化物とMnSとの複合析出物をフェライトの変態核として活用し、HAZの靭性を向上させる方法が提案されている。さらに、特許文献3ではTi窒化物とBNとの複合析出物を粒界フェライトの析出核として活用し、HAZ靭性を向上させる方法が提案されている。   Conventionally, many proposals have been made focusing on the HAZ toughness of steel materials to which the high heat input welding method is applied. For example, as disclosed in Patent Document 1 and the like, there is a method of reducing the HAZ austenite grains and improving toughness by securing fine Ti nitrides in the steel. Patent Document 2 proposes a method for improving the toughness of HAZ by utilizing a composite precipitate of Ti nitride and MnS as a transformation nucleus of ferrite. Further, Patent Document 3 proposes a method for improving HAZ toughness by utilizing a composite precipitate of Ti nitride and BN as precipitation nuclei of grain boundary ferrite.

しかしながら、このTi窒化物は、HAZのうち最高到達温度が1400℃を超える溶接金属との境界(以下、溶接ボンド部とも称する。)近傍ではほとんど固溶してしまうので、靭性向上効果が低下してしまうという問題がある。そのため、上記のようなTi窒化物を利用した鋼材では、近年のHAZ靭性に対する厳しい要求や、超大入熱溶接におけるHAZ靭性の必要特性を達成することが困難である。   However, since this Ti nitride is almost dissolved in the vicinity of the boundary (hereinafter also referred to as a weld bond portion) with the weld metal having a maximum ultimate temperature exceeding 1400 ° C. of HAZ, the effect of improving toughness is reduced. There is a problem that it ends up. For this reason, it is difficult for steel materials using Ti nitride as described above to achieve the strict requirements for HAZ toughness in recent years and the required characteristics of HAZ toughness in super-high heat input welding.

この溶接ボンド部近傍の靭性を改善する方法として、Ti酸化物を含有した鋼が厚板、形鋼などの様々な分野で使用されている。例えば、厚板分野では特許文献4や特許文献5に例示されているように、Ti酸化物を含有した鋼が大入熱溶接部靭性向上に非常に有効であり、高張力鋼への適用が有望である。この原理は、鋼の融点においても安定なTi酸化物をサイトとして、溶接後の温度低下途中にTi窒化物、MnS等が析出し、さらにそれらをサイトとして微細フェライトが生成し、その結果、靭性に有害な粗大フェライトの生成が抑制されて、靭性の劣化が防止できるというものである。   As a method for improving the toughness in the vicinity of the weld bond portion, steel containing Ti oxide is used in various fields such as thick plates and section steel. For example, as exemplified in Patent Document 4 and Patent Document 5 in the thick plate field, steel containing Ti oxide is very effective in improving the toughness of a high heat input weld, and is applicable to high-tensile steel. Promising. This principle is based on Ti oxide, which is stable even at the melting point of steel, and Ti nitride, MnS, etc. are precipitated in the middle of the temperature drop after welding, and fine ferrite is formed using these as sites, resulting in toughness. The generation of coarse ferrite that is harmful to steel is suppressed, and deterioration of toughness can be prevented.

しかしながら、このようなTi酸化物は、鋼中へ分散される個数をあまり多くすることができないという問題がある。その原因は、Ti酸化物の粗大化や凝集合体であり、Ti酸化物の個数を増加させようとすれば5μm以上の粗大なTi酸化物、いわゆる介在物が増加してしまうためと考えられる。この5μm以上の介在物は、構造物の破壊の起点となったり、靭性の低下を引き起こしたりして、有害であるため回避すべきものである。そのため、さらなるHAZ靭性の向上を達成するためには、粗大化や凝集合体が起こりにくく、Ti酸化物よりも微細に分散する酸化物を活用する必要があった。   However, such a Ti oxide has a problem that the number dispersed in steel cannot be increased too much. The cause is considered to be coarsening or aggregation of Ti oxides, and if the number of Ti oxides is increased, coarse Ti oxides of 5 μm or more, so-called inclusions are increased. This inclusion of 5 μm or more should be avoided because it is harmful because it becomes a starting point of destruction of the structure or causes a decrease in toughness. Therefore, in order to achieve further improvement in HAZ toughness, it is necessary to utilize an oxide that is less likely to be coarsened or aggregated and is more finely dispersed than Ti oxide.

また、このようなTi酸化物の鋼中への分散方法としては、Al等の強脱酸元素を実質的に含まない溶鋼中へのTi添加によるものが多い。しかしながら、単に溶鋼中にTiを添加するだけでは鋼中のTi酸化物の個数、分散度を制御することは困難であり、さらには、TiN、MnS等の析出物の個数、分散度を制御することも困難である。そのため、Ti脱酸のみによってTi酸化物を分散させた鋼においては、例えば、Ti酸化物の個数が充分ではなかったり、厚板の板厚方向の靭性変動を生じたりする問題があった。   Further, as a method of dispersing such Ti oxide in steel, there are many methods by adding Ti to molten steel which does not substantially contain a strong deoxidizing element such as Al. However, it is difficult to control the number of Ti oxides and the degree of dispersion in the steel simply by adding Ti to the molten steel. Further, the number and the degree of dispersion of precipitates such as TiN and MnS are controlled. It is also difficult. Therefore, in steel in which Ti oxide is dispersed only by Ti deoxidation, for example, there are problems that the number of Ti oxides is not sufficient or that the toughness variation in the thickness direction of the thick plate occurs.

さらに、上記特許文献4などの方法では、Ti酸化物を生成しやすくするために、Al量の上限を、0.007%という非常に少ない量で制限している。そのため、鋼材中のAl量が少ない場合、AlN析出物量の不足などの原因により、母材の靭性が低下する場合があった。また、通常使用されている溶接材料を用いてAl量の少ない鋼板を溶接した場合、溶接金属の靭性が低下する場合があった。   Furthermore, in the method disclosed in Patent Document 4 and the like, the upper limit of the Al amount is limited to a very small amount of 0.007% in order to easily generate a Ti oxide. Therefore, when the amount of Al in the steel material is small, the toughness of the base material may be lowered due to a shortage of the amount of AlN precipitates. Further, when a steel sheet having a small Al content is welded using a commonly used welding material, the toughness of the weld metal may be lowered.

このような問題に対して、特許文献6や特許文献7において、Ti添加直後のAl添加、あるいはAl、Ca複合添加で、生成するTi−Al複合酸化物やTi、Al、Caの複合酸化物を活用する技術が提案されている。このような技術により、大入熱溶接HAZ靭性を大幅に向上させることが可能となった。   In order to solve such a problem, in Patent Document 6 and Patent Document 7, Ti—Al composite oxide or composite oxide of Ti, Al, and Ca generated by adding Al immediately after adding Ti or adding Al and Ca composite. A technology that utilizes the above has been proposed. With such a technique, it has become possible to greatly improve the high heat input welding HAZ toughness.

特公昭55−026164号公報Japanese Patent Publication No. 55-026164 特開平03−264614号公報Japanese Patent Laid-Open No. 03-264614 特開平04−143246号公報Japanese Patent Laid-Open No. 04-143246 特開昭61−079745号公報JP 61-079745 A 特開昭62−103344号公報JP-A-62-103344 特開平06−293937号公報Japanese Patent Laid-Open No. 06-293937 特開平10−183295号公報JP-A-10-183295

しかしながら、造船業界、建設業界においては、近年、20kJ/mm以上の大入熱溶接、大きいものでは100kJ/mmにもなる大入熱溶接の適用が検討されるようになり、上記の特許文献5〜7などの従来手法より飛躍的に溶接熱影響部靱性を向上させた鋼材が必要とされるようになってきた。さらに、強度確保の点から炭素当量(Ceq)を0.35以上に高めた場合では、従来手法ではHAZ靭性、特に溶接ボンド部近傍の靭性向上が大きく低下することから更なる改善が必要とされるようになった。   However, in the shipbuilding industry and the construction industry, in recent years, application of large heat input welding of 20 kJ / mm or more, and large heat input welding of 100 kJ / mm at large has been studied. Steel materials having dramatically improved weld heat-affected zone toughness than conventional methods such as ˜7 have been required. Furthermore, when the carbon equivalent (Ceq) is increased to 0.35 or more from the viewpoint of securing strength, the conventional method requires a further improvement because the HAZ toughness, particularly the toughness improvement in the vicinity of the weld bond portion, is greatly reduced. It became so.

そこで、本発明は、Ceqが0.35以上0.40以下の鋼材で、入熱20〜100kJ/mmの大入熱溶接においても優れたHAZ靭性を実現できる、入熱20〜100kJ/mmの大入熱溶接用高HAZ靭性鋼材を提供することを目的とするものである。   Therefore, the present invention is a steel material having a Ceq of 0.35 or more and 0.40 or less, and can realize excellent HAZ toughness even in a large heat input welding with a heat input of 20 to 100 kJ / mm, with a heat input of 20 to 100 kJ / mm. An object of the present invention is to provide a high HAZ toughness steel material for high heat input welding.

本発明者らは、Ceqが0.35以上0.40以下の鋼材で大入熱溶接がなされたときのHAZ部の金属組織を添加元素の適正化により制御することで達成することを着想した。以下に、本発明がなされるまでの経緯を説明する。   The present inventors have conceived that this can be achieved by controlling the metallographic structure of the HAZ part by optimizing the additive elements when high heat input welding is performed with a steel material having a Ceq of 0.35 or more and 0.40 or less. . The background until the present invention is made will be described below.

再加熱オーステナイト粒を細粒化するためには、前述のとおり、高温でのオーステナイト粒の成長を抑制することが必要である。その手段として最も有効な方法は、分散粒子によりオーステナイトの粒界をピンニングし、粒界の移動を止める方法が考えられる。そのような作用をする分散粒子としては、従来、Ti窒化物(特許文献1〜3参照)や、1400℃以上の高温で安定なTi酸化物(特許文献4、5参照)がピンニング粒子として活用されてきた。そして、分散粒子による結晶粒界のピンニング効果は、分散粒子の体積率が大きいほど大きいことから、Al、Caを随時脱酸元素として用いて酸化物の体積分率を大きくし、かつ適正な粒子径とする方法が提案されてきた(特許文献6、7参照)。これにより、HAZの再加熱オーステナイト粒はピンニングにより極めて有効に細粒化し、HAZ靭性もそれに伴い向上する。   In order to refine the reheated austenite grains, it is necessary to suppress the growth of the austenite grains at a high temperature as described above. The most effective method for that is to pin the austenite grain boundaries with dispersed particles and stop the grain boundary movement. As the dispersed particles having such an action, conventionally, Ti nitrides (see Patent Documents 1 to 3) and Ti oxides stable at a high temperature of 1400 ° C. or higher (see Patent Documents 4 and 5) are utilized as pinning particles. It has been. And, since the pinning effect of the grain boundaries by the dispersed particles is larger as the volume fraction of the dispersed particles is larger, the volume fraction of the oxide is increased by using Al and Ca as occasional deoxidizing elements, and appropriate particles are obtained. A method of making the diameter has been proposed (see Patent Documents 6 and 7). Thereby, the reheated austenite grains of HAZ are refined very effectively by pinning, and the HAZ toughness is improved accordingly.

しかし、溶接入熱が20〜100kJ/mmと大入熱である場合、特にCeqが0.35以上0.40以下の鋼材ではHAZ組織が上部ベイナイト主体の粗い組織となるため十分なHAZ靭性が得られないという問題が新たに生じた。従って、HAZ靭性を改善するためには、粒内の組織を細かくすることが必要であると考えた。そして、粒内のベイナイト組織を細かくするにはBの添加が有効であることを見出した。   However, when the welding heat input is a large heat input of 20 to 100 kJ / mm, the HAZ structure becomes a coarse structure mainly composed of upper bainite, particularly in steel materials having a Ceq of 0.35 or more and 0.40 or less, so that sufficient HAZ toughness is obtained. A new problem has arisen. Therefore, in order to improve the HAZ toughness, it was considered necessary to make the structure in the grains fine. And it discovered that addition of B was effective in order to make the bainite structure in a grain fine.

しかし、単にBを添加するだけでは粒内のベイナイト組織を細かくしない場合がある。そこで、本発明者らは更に詳細検討した。その結果、下記(2)式で示されるEBが−0.0012以上0以下を満たすことにより粒内の組織が針状のフェライトを含む微細な組織となることを見出した。   However, simply adding B may not make the bainite structure in the grains fine. Therefore, the present inventors have further studied in detail. As a result, it was found that when the EB represented by the following formula (2) satisfies −0.0012 or more and 0 or less, the structure in the grains becomes a fine structure including acicular ferrite.

本発明は、以上の知見に基づき、さらに検討を重ねてはじめてなされたものであり、その要旨は、下記のとおりである。
(1)質量%で、C:0.03〜0.18%、Si:0.01〜0.50%、Mn:0.40〜2.00%、Al:0.005〜0.017%、Ti:0.005〜0.030%、Ca:0.0005〜0.0050%、N:0.0010〜0.0100%、B:0.0002〜0.0024%を含有し、P:0.020%以下、S:0.020%以下であり、残部はFeおよび不可避不純物からなり、かつ、下記(1)式で示される炭素当量(Ceq)が0.35≦Ceq≦0.40、下記(2)式で示される固溶B量(EB)が−0.0012≦EB≦0を満たし、45kJ/mm相当の溶接熱サイクルを付与したときの再現HAZ組織のオーステナイト粒の平均粒径が250μm以下であることを特徴とする、入熱20〜100kJ/mmの大入熱溶接用高HAZ靭性鋼材。
Ceq=C+Mn/6+(Cr+Mo+V)/5+(Ni+Cu)/15 (1)
EB=B−0.77×N+0.23×Ti (2)
ただし、C、Mn、Cr、Mo、V、Ni、Cu、B、N、Tiは、各元素の含有量(質量%)である。
(2)さらに選択元素として、質量%で、Cu:0.10〜1.00%、Ni:0.10〜4.00%、Nb:0.005〜0.100%、V:0.010〜0.100%、Cr:0.01〜0.60%、Mo:0.01〜0.60%、Mg:0.0002〜0.0050%、REM:0.0002〜0.1000%の1種または2種以上を含有することを特徴とする、上記(1)に記載の入熱20〜100kJ/mmの大入熱溶接用高HAZ靭性鋼材。
The present invention has been made for the first time after further studies based on the above findings, and the gist thereof is as follows.
(1) By mass%, C: 0.03 to 0.18%, Si: 0.01 to 0.50%, Mn: 0.40 to 2.00%, Al: 0.005 to 0.017 % Ti: 0.005-0.030%, Ca: 0.0005-0.0050%, N: 0.0010-0.0100%, B: 0.0002-0.0024%, P: 0.020% or less, S: 0.020% or less, the balance is Fe and inevitable impurities, and the carbon equivalent (Ceq) represented by the following formula (1) is 0.35 ≦ Ceq ≦ 0.40 The average grain size of austenite grains with a reproducible HAZ structure when the amount of dissolved B (EB) represented by the following formula (2) satisfies −0.0012 ≦ EB ≦ 0 and a welding heat cycle equivalent to 45 kJ / mm is applied. Heat input 20-100 kJ /, characterized in that the diameter is 250 μm or less mm high HAZ toughness steel for high heat input welding.
Ceq = C + Mn / 6 + (Cr + Mo + V) / 5 + (Ni + Cu) / 15 (1)
EB = B−0.77 × N + 0.23 × Ti (2)
However, C, Mn, Cr, Mo, V, Ni, Cu, B, N, and Ti are content (mass%) of each element.
(2) Further, as selective elements, in mass%, Cu: 0.10 to 1.00%, Ni: 0.10 to 4.00%, Nb: 0.005 to 0.100%, V: 0.010 -0.100%, Cr: 0.01-0.60%, Mo: 0.01-0.60%, Mg: 0.0002-0.0050%, REM: 0.0002-0.1000% The high HAZ toughness steel material for high heat input welding having a heat input of 20 to 100 kJ / mm as described in the above (1), comprising one or more kinds.

本発明は、船舶、海洋構造物、中高層ビルなどの破壊に対する厳しい靭性要求を満足する鋼板を供給するものであり、この種の産業分野にもたらす効果は極めて大きく、さらに構造物の安全性の意味から社会に対する貢献も非常に大きい。   The present invention supplies steel sheets that satisfy severe toughness requirements for the destruction of ships, offshore structures, mid-to-high-rise buildings, etc., and has an extremely large effect on this type of industrial field. Further, it means the safety of structures. The contribution to society is very large.

以下、本発明の実施の形態について詳細に説明する。   Hereinafter, embodiments of the present invention will be described in detail.

本発明は、船舶、海洋構造物、中高層ビル、橋梁などに使用される溶接構造用鋼材全般に加えて、鋼管用素材の鋼板、棒鋼、条鋼、熱延鋼板などにも適用可能であり、いずれの場合も溶接継手部の靭性の大幅向上が得られるものである。   The present invention can be applied to steel pipe materials, steel bars, strips, hot-rolled steel sheets, etc., in addition to general steel materials for welded structures used in ships, offshore structures, medium-rise buildings, bridges, etc. In this case, the toughness of the welded joint can be greatly improved.

まず、本発明の基本成分範囲の限定理由について述べる。   First, the reasons for limiting the basic component range of the present invention will be described.

Cは、鋼の強度を向上させる有効な成分として下限を0.03%とし、また過剰の添加は、鋼材の溶接性やHAZ靭性などを著しく低下させるので、上限を0.18%とした。   C is an effective component for improving the strength of steel, and the lower limit is set to 0.03%. Excessive addition significantly reduces the weldability and HAZ toughness of the steel material, so the upper limit is set to 0.18%.

Siは、母材の強度確保、脱酸などに必要な成分であり0.01%以上添加するが、HAZの硬化により靭性が低下するのを防止するため上限を0.50%とした。   Si is a component necessary for securing the strength of the base material, deoxidation and the like, and is added in an amount of 0.01% or more, but the upper limit was made 0.50% in order to prevent the toughness from being lowered by the hardening of HAZ.

Mnは、母材の強度、靭性の確保に有効な成分として0.40%以上の添加が必要であるが、溶接部の靭性、割れ性などの許容できる範囲で上限を2.00%とした。   Mn needs to be added in an amount of 0.40% or more as an effective component for securing the strength and toughness of the base material, but the upper limit is set to 2.00% within an acceptable range of toughness and cracking of the welded portion. .

Pは、含有量が少ないほど望ましいが、これを工業的に低減させるためには多大なコストがかかることから、許容範囲を0.020%以下とした。   The smaller the content of P, the better. However, in order to reduce this industrially, it takes a great deal of cost, so the allowable range was set to 0.020% or less.

Sは、含有量が少ないほど望ましいが、これを工業的に低減させるためには多大なコストがかかることから、許容範囲を0.020%以下とした。   The content of S is preferably as small as possible. However, since it takes a great deal of cost to reduce this industrially, the allowable range is set to 0.020% or less.

Alは、重要な脱酸元素であり、下限値を0.005%とした。また、Alが多量に存在すると、鋳片の表面品位が劣化するため、上限を0.070%とした。なお、Al量の上限は、実施例に基づき、0.017%以下とする。 Al is an important deoxidizing element, and the lower limit was set to 0.005%. In addition, when Al is present in a large amount, the surface quality of the slab deteriorates, so the upper limit was made 0.070%. Note that the upper limit of the Al content is 0.017% or less based on the examples.

Tiは、Nと結合してTi窒化物を形成させるために0.005%以上添加する。しかし、固溶Ti量が増加するとHAZ靭性が低下するため、0.030%を上限とした。   Ti is added in an amount of 0.005% or more in order to combine with N to form Ti nitride. However, since the HAZ toughness decreases as the amount of dissolved Ti increases, the upper limit is set to 0.030%.

Caは、Ca系酸化物を生成させるために0.0005%以上の添加が必要である。しかしながら、過剰の添加は粗大介在物を生成させるため、0.0050%を上限とした。   Ca needs to be added in an amount of 0.0005% or more in order to produce a Ca-based oxide. However, excessive addition generates coarse inclusions, so 0.0050% was made the upper limit.

Nは、Tiと結合してTi窒化物を形成させるために0.0010%以上添加するが、量が増えると固溶Nが増大しHAZ靭性の低下を招くことから0.0100%を上限とした。   N is added in an amount of 0.0010% or more in order to combine with Ti to form Ti nitride. However, as the amount increases, the solid solution N increases and the HAZ toughness is lowered, so 0.0100% is made the upper limit. did.

Bは、加熱オーステナイト粒界に生成するフェライトの成長を抑制する上で有効な元素であり、少なくとも0.0002%添加する。しかし、多量に添加すると鋼材の靭性を劣化させるため、上限を0.0024%とした。 B is an element effective in suppressing the growth of ferrite generated at the heated austenite grain boundary, and is added at least 0.0002%. However, if added in a large amount, the toughness of the steel material is deteriorated, so the upper limit was made 0.0024 %.

Cuは、鋼材の強度および耐食性を向上させるために必要に応じて0.10%以上添加するが、1.00%を越えるとHAZ靭性を低下させることから、1.00%を上限とした。   Cu is added in an amount of 0.10% or more as necessary in order to improve the strength and corrosion resistance of the steel material. However, if it exceeds 1.00%, the HAZ toughness is lowered, so the upper limit was made 1.00%.

Niは、母材靭性を大きく低下させずに強度を向上させ、またHAZ靭性を改善させる傾向があることから必要に応じて0.10%以上添加するが、4.00%超の添加は製造コストを上昇させることから、Niの範囲を0.10%以上4.00%以下とした。   Ni tends to improve strength without significantly reducing the toughness of the base metal and also improve HAZ toughness. Therefore, Ni is added in an amount of 0.10% or more as necessary. In order to increase the cost, the range of Ni is set to 0.10% to 4.00%.

Nbは、焼き入れ性を向上させることにより母材の強度を向上させるために有効な元素であり必要に応じて添加するが、0.005%未満の添加では十分な強度上昇が得られず、また0.100%を超える過剰な添加は母材の靭性を著しく低下させることから、Nbの添加範囲を0.005%以上0.100%以下とした。   Nb is an effective element for improving the strength of the base material by improving the hardenability, and is added as necessary. However, if the addition is less than 0.005%, a sufficient strength increase cannot be obtained. Further, excessive addition exceeding 0.100% significantly reduces the toughness of the base metal, so the Nb addition range was set to 0.005% or more and 0.100% or less.

Vは、母材の強度を向上させるために有効な元素であり、必要に応じて0.010%以上添加するが、過剰な添加は母材靭性を著しく低下させることから、それぞれ0.100%を上限とした。   V is an element effective for improving the strength of the base material, and is added in an amount of 0.010% or more as necessary. However, excessive addition significantly reduces the base material toughness. Was the upper limit.

Cr、Moもまた母材の強度を向上させるために有効な元素であることから必要に応じて0.01%以上添加するが、ともに過剰な添加は母材靭性を著しく低下させることから、それぞれ0.60%、0.60%を上限とした。   Since Cr and Mo are also effective elements for improving the strength of the base material, 0.01% or more is added as necessary. However, excessive addition significantly reduces the base material toughness, respectively. The upper limits were 0.60% and 0.60%.

Mg、REMは、いずれも溶鋼中Caに次ぐ脱酸力を有し、Caによる微細酸化物形成を補助する働きがあることからともに必要に応じて0.0002%以上添加するが、過剰に入れるとCaと比較してコストアップが大きいとともに、粗大介在物を作って鋼板およびHAZの靭性を阻害することから、それぞれの上限を0.0050%、0.1000%とした。   Both Mg and REM have deoxidizing power next to Ca in molten steel, and have the function of assisting the formation of fine oxides by Ca. Compared with Ca, the cost increase is large, and coarse inclusions are formed to inhibit the toughness of the steel sheet and the HAZ. Therefore, the upper limits were set to 0.0050% and 0.1000%, respectively.

次に、上述(2)式で示されるEB値の限定理由について説明する。   Next, the reason for limiting the EB value represented by the above equation (2) will be described.

発明者らは上述の通り、HAZ靭性改善に粒内のベイナイト組織の細粒化が必要と考え、そのためにはBの添加が有効であることを見出した。45kJ/mm相当の溶接熱サイクルを付与したときの再現HAZ組織中のオーステナイト粒界から生成する組織が、B無添加時には上部ベイナイトの塊が主体であったものが、B添加により針状に伸びたフェライトが占める割合の多い組織へと変化し、組織が微細になることを見出した。但し、単にBを添加するだけでは全面が上部ベイナイト組織となり、HAZ靭性が改善しないどころかかえって低下することがある。   As described above, the inventors considered that it is necessary to refine the bainite structure in the grains to improve the HAZ toughness, and for that purpose, the addition of B was found to be effective. The structure formed from the austenite grain boundary in the reproduced HAZ structure when a welding heat cycle equivalent to 45 kJ / mm is applied, which was mainly composed of upper bainite lumps when B was not added, was elongated in a needle shape by addition of B. It was found that the structure changed to a structure with a large proportion of ferrite and the structure became finer. However, if B is simply added, the entire surface becomes an upper bainite structure, and the HAZ toughness may not be improved, but may decrease.

そこで、本発明者らが更に鋭意検討した結果、Bが固溶している状態であることがHAZ靭性が改善しない原因のひとつであることを見出した。そして、Bと化合物を形成するTi、Nを含む上述(2)式で示される固溶B量(EB)を指標として、HAZ靭性との関係を検討した。   Therefore, as a result of further intensive studies by the present inventors, it was found that the state in which B is in a solid solution is one of the causes that the HAZ toughness is not improved. And the relationship with HAZ toughness was examined by using as an index the solid solution B amount (EB) represented by the above formula (2) containing Ti and N forming compounds with B.

検討には、45kJ/mm相当の溶接熱サイクルを付与したときの再現HAZ組織(以下単に「再現HAZ組織」ともいう。)を用いた。45kJ/mm相当の溶接熱サイクルとは、熱サイクル試験片を用いて、板厚65mmの鋼板を入熱45kJのエレクトロガス溶接を施した際に得られるHAZのいくつかの部位から得られた熱履歴をもとに解析した板厚中心の溶融線での熱履歴を意味する。より具体的には、図1に示すように、室温から最高加熱温度1400℃まで40秒で加熱し、この最高加熱温度に25秒間保持した後、800℃から500℃までを5分間かけて冷却する熱履歴を意味する。   In the examination, a reconstructed HAZ structure when a welding heat cycle equivalent to 45 kJ / mm was applied (hereinafter also simply referred to as “reproduced HAZ structure”) was used. Welding heat cycle equivalent to 45 kJ / mm means heat obtained from several parts of HAZ obtained when electrogas welding of heat input of 45 kJ is performed on a steel plate having a thickness of 65 mm using a heat cycle test piece. It means the thermal history at the melting line at the center of the thickness analyzed based on the history. More specifically, as shown in FIG. 1, heating is performed from room temperature to a maximum heating temperature of 1400 ° C. in 40 seconds, held at this maximum heating temperature for 25 seconds, and then cooled from 800 ° C. to 500 ° C. over 5 minutes. It means the heat history to do.

その結果、図2に示すように、EBの値が0質量%以下の範囲であれば、再現HAZ組織中の針状に伸びたフェライトが占める割合の多い組織へと変化し組織が微細になることを見出した。そして図3に示すように、オーステナイト粒の粒径が250μm以下であり、かつ、EBの値が−0.0012質量%以上0質量%以下の範囲であれば、再現HAZ組織が上述の微細組織となり、再現HAZ靱性は、−20℃におけるシャルピー吸収エネルギー値で−100J以上となり、目標とする靭性が得られることを見出した。図3において、「オーステナイト粗大」と記載したプロット以外のプロットについては平均オーステナイト粒径が250μm以下である。また、EBの値が−0.0012質量%未満のときに再現HAZ靭性が劣化する原因については明らかではないが、恐らくHAZ中の固溶N量が多いためと考えられる。   As a result, as shown in FIG. 2, when the value of EB is in the range of 0% by mass or less, the structure changes to a structure having a high proportion of the needle-shaped ferrite in the reproduced HAZ structure, and the structure becomes finer. I found out. As shown in FIG. 3, when the austenite grain size is 250 μm or less and the EB value is in the range of −0.0012 mass% to 0 mass%, the reproduced HAZ structure is the above-described microstructure. Thus, it was found that the reproduced HAZ toughness was -100 J or more in the Charpy absorbed energy value at -20 ° C, and the target toughness was obtained. In FIG. 3, the average austenite grain size is 250 μm or less for plots other than the plot described as “Austenite coarse”. Further, although the reason why the reproduced HAZ toughness deteriorates when the value of EB is less than −0.0012% by mass is not clear, it is probably because the amount of dissolved N in the HAZ is large.

なお、再現HAZ組織のオーステナイト粒を250μm以下に細粒化させる方法として本発明は、Caを0.0005質量%以上含有させることによって鋼中に微細酸化物を多数分散させ、酸化物のピンニングによって結晶粒を微細化する方法を用いることができる。溶鋼の精錬時に溶鋼をAl、Caにより逐次脱酸することで、より確実に鋼中に微細酸化物を多数分散させることが可能となる。   In addition, as a method of refining austenite grains having a reproduced HAZ structure to 250 μm or less, the present invention disperses a number of fine oxides in steel by containing Ca in an amount of 0.0005 mass% or more, and pinning the oxides. A method of refining crystal grains can be used. By sequentially deoxidizing the molten steel with Al and Ca during the refining of the molten steel, it becomes possible to more reliably disperse many fine oxides in the steel.

表1に示した化学成分で試験材を試作した。A1〜A19が本発明鋼、B1〜11が比較鋼である。試験材は真空溶解で溶製している。脱酸は、Ti投入前に溶鋼の溶存酸素をCで調整し、その後、B9およびB10以外の試験材についてはTi、Al、Caを順に添加し脱酸を行った。B9については、TiおよびAlを同時に添加し脱酸を行い、B10については、Ti、Al、Caを同時に添加し脱酸を行った。その後、これら鋼材を1200℃に加熱し15mmの圧延材とし、熱サイクル試験片を採取した。得られた試験片に45kJ/mm相当の大入熱溶接を模擬した図1に示す熱サイクルを付与し、シャルピー衝撃試験による靭性を評価した。靭性は、各試験材を−20℃で3本ずつ試験して得られた平均のエネルギー値で評価した。各試験材の再現HAZ組織の金属組織は、ナイタール腐食して光学顕微鏡により観察した。具体的には、オーステナイト粒の測定は50倍の倍率で撮影した写真(160mm×200mm)から切断法から求めた。   Test materials were made with the chemical components shown in Table 1. A1 to A19 are invention steels, and B1 to 11 are comparative steels. The test material is melted by vacuum melting. Deoxidation was performed by adjusting the dissolved oxygen of the molten steel with C before adding Ti, and then adding Ti, Al, and Ca in order for the test materials other than B9 and B10. For B9, Ti and Al were added simultaneously for deoxidation, and for B10, Ti, Al, and Ca were added simultaneously for deoxidation. Then, these steel materials were heated to 1200 ° C. to obtain 15 mm rolled materials, and heat cycle test pieces were collected. The obtained test piece was subjected to the thermal cycle shown in FIG. 1 simulating high heat input welding equivalent to 45 kJ / mm, and the toughness by the Charpy impact test was evaluated. Toughness was evaluated based on an average energy value obtained by testing three test materials at -20 ° C. The metal structure of the reproduced HAZ structure of each test material was subjected to nital corrosion and observed with an optical microscope. Specifically, the austenite grains were measured from a photograph (160 mm × 200 mm) taken at a magnification of 50 times by a cutting method.

表2には、式(1)で示されるCeq値、式(2)で示されるEB値、再現HAZ組織のオーステナイト粒径、およびHAZ靭性値を示す。   Table 2 shows the Ceq value represented by the formula (1), the EB value represented by the formula (2), the austenite grain size of the reproduced HAZ structure, and the HAZ toughness value.

表2から明らかなように、A1〜A19の本発明鋼は、−20℃におけるシャルピー衝撃試験での吸収エネルギー値が100J以上となり優れたHAZ靭性を有することが判る。   As is apparent from Table 2, the steels of the present invention A1 to A19 have an excellent HAZ toughness with an absorption energy value of 100 J or more in a Charpy impact test at -20 ° C.

一方、比較例のB1〜11は、いずれも−20℃におけるシャルピー吸収エネルギー値が100J以下となっておりHAZ靭性が低い。これらの原因は、いずれも本発明範囲から外れているためである。すなわち、B1〜8は、EB値が本発明範囲から外れているためである。B9は、脱酸条件が他鋼と異なり再現HAZ組織のオーステナイト粒の粗大化を抑制するに十分な微細酸化物が分散できていないため、オーステナイト粒径が250μmを超えて粗大になったためである。B10は、B9同様の理由に加え、Ceq値が低くHAZ組織が粗大なフェライト主体となったためである。B11はCeq値が高くHAZ組織が粗大な上部ベイナイト組織となったためである。   On the other hand, B1 to 11 of Comparative Examples all have Charpy absorbed energy values at −20 ° C. of 100 J or less and have low HAZ toughness. These causes are all out of the scope of the present invention. That is, B1 to 8 are because the EB values are out of the scope of the present invention. B9 is because the deoxidation condition is different from other steels, and the fine oxide sufficient to suppress the coarsening of the austenite grains of the reproduced HAZ structure cannot be dispersed, so the austenite grain size becomes coarser than 250 μm. . This is because B10 is mainly composed of ferrite having a low Ceq value and a coarse HAZ structure in addition to the same reason as B9. This is because B11 has an upper bainite structure having a high Ceq value and a coarse HAZ structure.

Figure 0004332064
Figure 0004332064

Figure 0004332064
Figure 0004332064

溶接入熱45kJ/mm相当の溶接熱影響部を再現する熱サイクル再現を示す図である。It is a figure which shows the thermal cycle reproduction which reproduces the welding heat affected zone of welding heat input 45kJ / mm equivalency. 固溶B量(EB値)と再現HAZ組織中に占める針状フェライトの面積分率との関係を示す図である。It is a figure which shows the relationship between the amount of solute B (EB value), and the area fraction of the acicular ferrite which occupies in reproduction | regeneration HAZ structure | tissue. 固溶B量(EB値)とHAZ靱性の関係を示す図である。It is a figure which shows the relationship between solid solution B amount (EB value) and HAZ toughness.

Claims (2)

質量%で、
C :0.03〜0.18%
Si:0.01〜0.50%
Mn:0.40〜2.00%
Al:0.005〜0.017
Ti:0.005〜0.030%
Ca:0.0005〜0.0050%
N :0.0010〜0.0100%
B :0.0002〜0.0024%を含有し、
P :0.020%以下
S :0.020%以下であり、
残部はFeおよび不可避不純物からなり、かつ、下記(1)式で示される炭素当量(Ceq)が0.35≦Ceq≦0.40、下記(2)式で示される固溶B量(EB)が−0.0012≦EB≦0を満たし、45kJ/mm相当の溶接熱サイクルを付与したときの再現HAZ組織のオーステナイト粒の平均粒径が250μm以下であることを特徴とする、
入熱20〜100kJ/mmの大入熱溶接用高HAZ靭性鋼材。
Ceq=C+Mn/6+(Cr+Mo+V)/5+(Ni+Cu)/15 (1)
EB=B−0.77×N+0.23×Ti (2)
ただし、C、Mn、Cr、Mo、V、Ni、Cu、B、N、Tiは、各元素の含有量(質量%)である。
% By mass
C: 0.03-0.18%
Si: 0.01 to 0.50%
Mn: 0.40 to 2.00%
Al: 0.005 to 0.017 %
Ti: 0.005-0.030%
Ca: 0.0005 to 0.0050%
N: 0.0010 to 0.0100%
B: 0.0002 to 0.0024% is contained,
P: 0.020% or less S: 0.020% or less,
The balance is Fe and inevitable impurities, and the carbon equivalent (Ceq) represented by the following formula (1) is 0.35 ≦ Ceq ≦ 0.40, and the solid solution B amount (EB) represented by the following formula (2) The average particle size of the austenite grains of the reproduced HAZ structure when satisfying −0.0012 ≦ EB ≦ 0 and applying a welding heat cycle corresponding to 45 kJ / mm is 250 μm or less,
A high HAZ toughness steel material for large heat input welding with a heat input of 20 to 100 kJ / mm.
Ceq = C + Mn / 6 + (Cr + Mo + V) / 5 + (Ni + Cu) / 15 (1)
EB = B−0.77 × N + 0.23 × Ti (2)
However, C, Mn, Cr, Mo, V, Ni, Cu, B, N, and Ti are content (mass%) of each element.
さらに、質量%で、選択元素として
Cu:0.10〜1.00%
Ni:0.10〜4.00%
Nb:0.005〜0.100%
V :0.010〜0.100%
Cr:0.01〜0.60%
Mo:0.01〜0.60%
Mg:0.0002〜0.0050%
REM:0.0002〜0.1000%
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に記載の入熱20〜100kJ/mmの大入熱溶接用高HAZ靭性鋼材。
Furthermore, as a selection element by mass%, Cu: 0.10 to 1.00%
Ni: 0.10 to 4.00%
Nb: 0.005 to 0.100%
V: 0.010-0.100%
Cr: 0.01-0.60%
Mo: 0.01-0.60%
Mg: 0.0002 to 0.0050%
REM: 0.0002 to 0.1000%
The high HAZ toughness steel material for large heat input welding with a heat input of 20 to 100 kJ / mm according to claim 1, characterized by containing one or more of the following.
JP2004138064A 2004-05-07 2004-05-07 High HAZ toughness steel for high heat input welding with heat input of 20-100 kJ / mm Expired - Fee Related JP4332064B2 (en)

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