JPH0126797B2 - - Google Patents
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- JPH0126797B2 JPH0126797B2 JP54088926A JP8892679A JPH0126797B2 JP H0126797 B2 JPH0126797 B2 JP H0126797B2 JP 54088926 A JP54088926 A JP 54088926A JP 8892679 A JP8892679 A JP 8892679A JP H0126797 B2 JPH0126797 B2 JP H0126797B2
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Description
本発明は高張力鋼の溶接法に関し、特に引張強
さが80Kg/mm2級以上の高張力鋼を予熱なしで溶接
する方法に関するものである。
近年、各の鋼構造物はますます大型化する傾向
にあり、重量の軽減、製造コストの低減並びに製
造時間の短縮等を図る為、高張力鋼に対する需要
は年々大幅に増大しており、すでに60Kg/mm2級
(以下Kg/mm2級をキロ級と略記する)の高張力鋼
については、各分野で広く使用されている。
しかし現在市販されている80キロ級高張力鋼で
は、高強度を確保する為に多量の合金元素を含有
させる必要があり、その結果PCM(後述する)が
高くなつて耐溶接割れ感受性が極端に悪化する。
もつとも溶接時の低温割れを防止する方法として
溶接前に母材を予熱する方法も有効であるが、80
キロ級高張力鋼では60キロ級高張力鋼に比べて相
当高い予熱温度を採用しなければならず、溶接施
工性の難点からごく僅かの用途にしか使用されて
いないのが現状である。
これらの事情から、溶接時の低温割れを防止す
る対策が種々検討され、たとえば以下に示す様な
方法が提案されている。
溶接材料については水素量の低減及び難吸湿
タイプ化。
構造物の設計施工においては拘束応力の緩
和。
鋼材については溶接硬化性の低減。
しかしこれらの方法しても80キロ級高張力鋼を
溶接するには相当高温に予熱することが不可欠で
あり、予熱なしで溶接割れを完全に防止し得る様
な技術は提案されていない。
本発明者等はかねてより80キロ級高張力鋼を予
熱なしでも溶接割れを起こすことなく溶接し得る
様な方法の開発を期して種々研究を重ね、特に鋼
材と溶接材料の両者の成分組成等を特定してやれ
ば上記の目的が達成できるのではないかと考え、
その線に沿つて研究を進めてきた。その結果、鋼
材の化学成分等を以下に示す様に調整すると共
に、以下に示す様な限られた化学成分の溶接材料
を使用すれば、上記の目的が見事に達成されるこ
とを知り、茲に本発明を完成するに至つた。
即ち本発明に係る溶接方法の構成とは、
C:0.04〜0.09%(重量%:以下同様)、Si:
0.55%以下、Mn:0.6〜1.4%、Cr:0.3%超1.0%
以下、Mo:0.3%超0.8%以下、V:0.1%以下、
B:0.0005〜0.002%、Al:0.04〜0.1%及びN:
0.002〜0.004%を必須成分とし、残部が鉄及び不
可避不純物であり、且つ下記〔〕式で算出され
るPCMが0.25%以下であると共に、焼入温度(T
〓)におけるAl量とN量の関係が下記〔〕式
で満足す鋼を焼入・焼戻処理してなる引張強さ80
Kg/mm2以上の耐溶接割れ感受性の優れた80Kg/mm2
級高張力鋼を母材とし、
〔〕…PCM=C(%)+1/30Si(%)+1/20Mn
(%)+1/20Cu(%)
+1/60Ni(%)+1/20Cr(%)+1/15Mo(%)
+1/10V(%)+5B(%)
下記組成即ち、
CaCO340〜60%、CaF210〜25%、Mn3〜5%、
Ni14〜8%、Cr0.5〜2.0%、Mo0.5〜2.0%を含む
と共に350〜2000℃におけるポテンシヤル水素量
が40PPm以下である被覆剤を軟鋼心線に被覆し
てなる高張力鋼用低水素系被覆アーク溶接棒を使
用して、前記母材を溶接するところに要旨が存在
する。この場合鋼材として上記した必須成分のほ
かCu:0.5%以下及び/若しくはNi:1.5%以下を
含有する80キロ級高張力鋼を使用すれば、溶接部
の性能を一段と高めることができる。
以下本発明の構成及び作用効果を、鋼材と溶接
材料に分けて説明するが、下記はもとより本発明
を限定する性質のものではなく、前・後記の趣旨
に沿つて適当に変更して実施することも可能であ
り、それらはすべて本発明技術の範疇に含まれ
る。
まず鋼材について説明する。
本発明者等は、前記した目的を達成する為には
80キロ級高張力鋼の耐溶接割れ感受性を高める必
要があると考え、その目安として現在比較的広く
使用されている60キロ級高張力鋼を基準とし、こ
れと同等及至上回る耐溶接割れ感受性の80キロ級
高張力鋼の開発を期して研究を行なつた。ところ
で耐溶接割れ感受性は、鋼材の最高硬さ及びPCM
に夫々反比例することが知られている。従つて60
キロ級鋼程度の耐溶接割れ感受性を確保する為に
は、80キロ級鋼に対して60キロ級鋼と同程度の最
高硬さ及びPCMを確保させる必要がある。ちなみ
に従来の60キロ級鋼の最高硬さはHv360以下、
PCMは0.25以下であるから、上記の目的を達成す
る為には、最高硬さ及びPCMを上記と同等及至そ
れ以下に抑える必要がある。
一方最高硬さはC含有量と密接な関係があり、
最高硬さを低くする為にはC含有量を少なくすれ
ばよいことも知られている。たとえば第1図は、
C含有量を種々変えて試作した鋼について行なつ
た最高硬さ試験の結果を示すグラフで、この結果
から、最高硬さをHv360以下に抑える為にはC含
有量を0.09%以下にすべきことが判る。しかしC
含有量を少なくすると鋼材の硬度は必然的に低下
するから、80キロ級程度の高張力を維持する為に
は他の合金元素量を増加しなければならない。
上記の知見をもとに本発明者等は、60キロ級高
張力鋼と同等若しくはそれ以上の耐溶接割れ感受
性を有する80キロ級高張力鋼、即ち最高硬さが
Hv360以下で且つPCMが0.25%以下であり、勿論
引張強さが80Kg/mm2以上である様な鋼材の開発を
目標に、まず低炭素鋼の焼入性に及ぼす合金元素
特にBの影響について検討した。
一般にBの焼入性倍数FBは、(A)式に示す様
にC含有量が減少するにつれて増大することが知
れている。
FB=1+1.5(0.9−C%) ……(A)
しかしこれらの関係が確認されているのはC量
が0.10%を超える領域のみであり、これ以下の低
C領域におけるBの焼入性倍数については推定さ
れていたにとどまる。
ところがC量を種々変化させた鋼材について行
なつたジヨミニー端焼入試験結果をもとに、C含
有量とBの焼入性倍数の関係を求めた結果第2図
に示す傾向が得られ、特にC量が0.10%以下の領
域におけるBの焼入性倍数は、相当のばらつきが
あるものの前記(A)式から推定される傾向(図中の
鎖線)よりも高い値を示すことが判つた。この様
な結果が得られたのは、低C領域ではB−C化合
物の析出が大幅に遅れると共にγ粒界への析出量
が大幅に低減する為と予想される。しかし第2図
からも明らかな様にBの焼入性倍数のばらつきは
極めて大きいから、Bの効果を確実に得る為には
ばらつきを可及的に少なくする必要がある。
そこで本発明は、前記ばらつきを少なくする為
の具体策について検討を進めた。そしてC含有量
が0.10%以下のものについてのBの焼入性倍数
を、N含有量との関係で整理したところ第3図に
示す結果が得られ、N含有量を規制することに
よつてBの焼入性倍数のばらつきが極めて小さく
なり、しかもN含有量が40PPm以下の領域で
は焼入性倍数が大幅に向上する、という新しい事
実を確認した。この理由については完全に解明し
た訳ではないが、N含有量の低い領域では粒界へ
のBN及びAlNの析出量が少なくなり、冷却時の
フエライト変態が大幅に遅れてマルテンサイトが
生成する為と考えられる。ちなみにAlは脱酸及
び結晶粒調整元素として有用な元素であるが、本
発明者等が実験によつて確認したところでは、
Alは上記効果のほか、B及びNの含有量との関
係において、焼入性向上に必要な固溶B量を安定
して確保するという極めて重要な作用がある。こ
れらの作用を有効に発揮させる為には少なくとも
0.04%以上含有させる必要があつた。しかしAlを
0.10%を超えて配合しても上記の効果は飽和状態
に達してそれ以上向上せず、むしろアルミナ系介
在物の量が増大して靭性及び板厚方向特性値が著
しく劣化するので、0.10%以下に抑えるべきであ
る。加えてAlは、先に述べた如くBの焼入性倍
数に及ぼすNの含有量と密接な関係を有し、満足
な焼入性倍数を確保する為には、任意の焼入温度
(T〓)におけるAl含有量とN含有量が前記
〔〕式を満足する様に成分調整しなければなら
ない。
即ち本発明においては、低C鋼中のN及びAl
の含有量を所定範囲に調整すると共に、焼入温度
におけるAl量とN量の間に一定の関係を持たせ
ることによつて、焼入性の良好な80キロ級高張力
鋼を得ることができる。たとえば第4図は、焼入
温度が900℃である場合に必要なAl及びNの含有
量の領域を図示したもので、斜線で示される範囲
が本発明の目的にかなう鋼を得る為の必須要件で
ある。尚焼入温度は鋼材の成分組成等によつて適
当に決められるが、最も好ましいのは(Ac3+50
℃)の温度である。
次に鋼材の成分範囲の前述の様に限定した理由
を補足説明する。
Cは、溶接硬化性の観点からできるだけ少ない
方が望ましく、Hv360以下の最高硬さを得る為に
は0.09%以下に抑えるべきである。しかし80キロ
級高張力鋼では、C含有量が0.04%未満になると
80Kg/mm2以上の引張り強さを確保するのに必要な
焼入硬さが得られなくなるので、少なくとも0.04
%以上含有させる必要がある。
Siは、この種のキルド鋼の場合、脱酸工程で必
然的に含まれてくる元素であり、また強度を高め
る作用も有している。しかし多すぎると溶接性や
靭性が損なわれるので、上限を0.55%とした。
Mnは、80キロ級高張力鋼として必要な強度と
靭性を確保するのに不可欠の元素であり、これら
の効果を有意に発揮させる為には少なくとも0.6
%以上含有させる必要がある。しかしMn含有量
が多すぎるとミクロ偏析及び溶接性の点で障害が
表わわれるので、1.4%以下に抑えるべきである。
Crは、焼入性を高める効果があり、80Kg/mm2
以上の引張り強度を確保する為には少なくとも
0.3%超含有させる必要がある。しかし多すぎる
と溶接性が低下するので1.0%以下に抑えねばな
らない。
Moは、鋼材の焼入性を一段と高め且つ焼戻し
軟化抵抗を高める作用があり、80Kg/mm2以上の引
張り強さを確保する為には0.3%超の添加が必要
である。しかし多量含有させると、溶接熱影響部
が硬化して耐溶接割れ感受性が劣化するほかコス
トも高くなるので、0.8%以下に止めるべきであ
る。
Vは、少量の添加で焼戻軟化抵抗を高め且つ強
度を高める作用があるが、多すぎると靭性が著し
く劣化するので0.1%以下に抑えるべきである。
Bは、極微量の添加で鋼の焼入性を著しく高め
る効果があり、これらの効果を有意に発揮させる
為には0.0005%以上含有させなければならない。
しかし0.002%を超えて含有させると、焼入時に
オーステナイト粒界にB−C化合物が多量生成
し、焼入性が劣化すると共に靭性も低下する。
Alは、先に詳述した理由から0.04〜0.1%の範
囲にすべきである。
NはB含有鋼にとつては一般に有害な元素とさ
れているが、前述の如く0.004%以下の低N鋼材
ではBの焼入性倍数を著しく向上させる。そして
0.002%未満でも低N化効果によつて焼入性は更
に向上するが、γ粒の微細化に寄与するAlN量
が不足する為γ粒が粗大化し、靭性が低下するの
で少なくとも0.002%以上含有させる必要がある。
Cuは、少量の添加で強度を高める効果がある
が、0.5%を超えて含有させてもそれ以上の強度
向上は殆んどみられず、むしろ溶接性及び表面性
状を劣化させるので0.5%以下に止めるべきであ
る。
Niは、強度及び靭性を高める効果があるが、
それらの効果はほぼ1.5%で飽和状態に達し、そ
れ以上の添加はコストを高めるだけであるので好
ましくない。
尚PCMは、溶接割れを防止する為に必要な予熱
温度を推定する為の指標とされるものである。従
来の60キロ級高張力鋼では、このPCMは通常0.25
%以下であり、80キロ級高張力鋼の溶接施工条件
を60キロ級鋼並みに改善する為には、このPCMを
0.25%以下に抑えることが必要である。
上記の如く本発明では、80キロ級高張力鋼の化
学成分殊にN及びBの含有率、任意の焼入温度に
おけるNとAlの含有量の関係並びにPCM等を適正
に調整することによつて、60キロ級高張力鋼に匹
敵し或はこれを上回る耐溶接割れ感受性を得るこ
とができるが、この鋼材を用た場合でも、予熱な
しで溶接割れが生じない様にする為には、下記成
分組成の被覆アーク溶接棒を使用する必要があ
り、これら両者の組み合わせによつてはじめて本
発明の最終目的が達成される。
即ち本発明では、溶接材料として、CaCO340
〜60%、CaF210〜25%、Mn3〜5%、Ni4〜8
%、Cr0.5〜20%、Mo0.5〜20%を含むと共に350
〜2000℃の温度範囲におけるポテンシヤル水素量
が40PPm以下である被覆剤を、軟鋼心線に被覆
した高張力鋼用低水素系被覆アーク溶接棒を使用
しなければならない。上記数値限定の理由は下記
の通りである。
Niは溶接金属の切欠靭性を高める作用があり
少なくとも4%以上含有させなければならない。
また8%を超えても高温側での靭性が低下し且つ
溶接割れが発生し易くなるのでこれ以下に止める
べきである。
Mnは3%以上含有させれば脱酸剤及び溶接金
属の強度及び靭性の改善、高温割れ防止に有効で
あるが、5%を超えると逆に靭性が悪化し低温割
れ発生し易くなる。
Cr及びMoは、溶接金属の強度向上に寄与す
る。溶接金属が80キロ級の強度を有するためそれ
ぞれ0.5%以上の添加が必要であるが多すぎると
靭性及び耐割れ性が低下する傾向があり、夫々2
%以下が好ましい。
更に本発明で極めて重要なことは、被覆剤中の
350〜2000℃の温度範囲におけるポテンシヤル水
素量(一般に溶接棒は、約350℃で乾燥しており、
乾燥した溶接棒を2000℃までの高温にしたときに
発生する水素量を測定した値をいう。)を40PPm
にしなければならないことである。即ち本発明者
等は、本発明の要件を満たす80キロ級高張力鋼
(第1表Aに示す鋼)を母材とし、80キロ級低水
素系被覆アーク溶接棒の被覆剤として350℃再乾
燥後のポテンシヤル水素量の異なるもの((第2
表)を使用してJIS Z 3158の斜めY形溶接割れ
試験を行なつた。25℃におけるルート割れ率の観
察結果として第5図が得られた。
第5図の結果からも明らかな様に、ルート割れ
率はポテンシヤル水素量が約80PPmを境界にし
急激に少なくなり、40PPm以下になるとルート
割れ率は零となる。これらの結果から、本発明で
は被覆剤中に含まれる元素の種類及び含有率を特
定すると共に、ポテンシヤル水素量を40PPm以
下にすることが不可欠の要件とされる。尚被覆剤
中のポテンシヤル水素量を40PPm以下にする手
段としては、ポテンシヤル水素の低い原料(例え
ば結晶水を含まない原料)及び吸湿性の小さい原
料と粘結剤を厳選使用し、並びに焼成時の温度及
び時間を適切に管理する方法等が挙げられる。
本発明は概略以上の様に構成されており、特定
成分組成の80キロ級高張力鋼と特定の80キロ級被
覆アーク溶接棒を使用することにより、以下の実
施例でも明らかにする如く予熱なしで溶接割れの
ない溶接を実施可能にしたものであつて、80キロ
級高張力鋼の溶接法として理想的な技術を提供す
るものである。
次に本発明の実施例を示す。
実施例 1
第1表に示す成分組成の80キロ級鋼板を母材と
し、第2表に示す成分組成の被覆剤(本発明棒
1,3、従来棒1,5)を軟鋼心線に被覆してな
る被覆アーク溶接棒を用いてJIS Z 3158による
斜めY形溶接割れ試験を行なつた。
結果を第3表に一括して示す。
The present invention relates to a method for welding high tensile strength steel, and particularly to a method for welding high tensile strength steel having a tensile strength of 80 Kg/mm 2 class or higher without preheating. In recent years, steel structures have become increasingly larger, and the demand for high-strength steel has increased significantly year by year in order to reduce weight, manufacturing costs, and manufacturing time. 60Kg/mm 2 class (hereinafter Kg/mm 2 class is abbreviated as kilo class) high tensile strength steel is widely used in various fields. However, the 80kg class high-strength steel currently on the market requires the inclusion of a large amount of alloying elements to ensure high strength, resulting in a high P CM (described later) and extreme susceptibility to weld cracking. worsens.
Of course, preheating the base material before welding is an effective way to prevent cold cracking during welding, but
Kilo-class high-tensile strength steel requires a considerably higher preheating temperature than 60-kg high-strength steel, and is currently only used in very few applications due to difficulties in welding workability. Under these circumstances, various measures to prevent cold cracking during welding have been studied, and the following methods have been proposed, for example. As for welding materials, we have reduced the amount of hydrogen and made them resistant to moisture absorption. Relaxation of restraint stress in the design and construction of structures. For steel materials, reduction of weld hardenability. However, even with these methods, preheating to a considerably high temperature is essential for welding 80 kg class high-strength steel, and no technology has been proposed that can completely prevent weld cracking without preheating. The present inventors have been conducting various researches for some time in the hope of developing a method that would be able to weld 80 kg class high-strength steel without preheating and without causing weld cracking, and in particular, the composition of both the steel material and the welding material. I thought that the above purpose could be achieved by identifying the
We have been conducting research along these lines. As a result, I learned that the above objectives could be achieved brilliantly by adjusting the chemical composition of the steel material as shown below, and by using welding materials with a limited chemical composition as shown below. The present invention was finally completed. That is, the composition of the welding method according to the present invention is as follows: C: 0.04 to 0.09% (weight %: the same applies hereinafter), Si:
0.55% or less, Mn: 0.6-1.4%, Cr: over 0.3% 1.0%
Below, Mo: more than 0.3% and 0.8% or less, V: 0.1% or less,
B: 0.0005-0.002%, Al: 0.04-0.1% and N:
0.002 to 0.004% is an essential component, the remainder is iron and unavoidable impurities, and P CM calculated by the following formula [] is 0.25% or less, and the quenching temperature (T
Tensile strength 80 obtained by quenching and tempering steel whose relationship between Al content and N content in 〓) satisfies the following formula []
80Kg/mm 2 with excellent weld cracking susceptibility over Kg/mm 2
Using grade high tensile strength steel as the base material, []...P CM = C (%) + 1/30Si (%) + 1/20Mn
(%) +1/20Cu (%) +1/60Ni (%) +1/20Cr (%) +1/15Mo (%) +1/10V (%) +5B (%) The following composition: CaCO 3 40-60%, CaF 2 10-25%, Mn 3-5%,
Low-strength steel for high-strength steel made by coating a mild steel core with a coating material containing 14-8% Ni, 0.5-2.0% Cr, and 0.5-2.0% Mo, and having a potential hydrogen content of 40PPm or less at 350-2000℃. The gist is that the base metal is welded using a hydrogen-based coated arc welding rod. In this case, the performance of the welded part can be further improved by using 80 kg class high tensile strength steel containing Cu: 0.5% or less and/or Ni: 1.5% or less in addition to the above-mentioned essential components. The structure, operation and effect of the present invention will be explained below separately for steel materials and welding materials, but the following does not limit the present invention, and may be implemented with appropriate changes in accordance with the spirit of the above and below. All of these are within the scope of the present technology. First, steel materials will be explained. The present inventors believe that in order to achieve the above-mentioned purpose,
We believe that it is necessary to improve the weld cracking resistance and susceptibility of 80 kg class high tensile strength steel, and as a guideline we use the 60 kg class high tensile strength steel, which is currently relatively widely used, as a standard, and develop products with equivalent or superior weld cracking susceptibility. Research was conducted with the aim of developing 80 kg class high tensile strength steel. By the way, weld cracking susceptibility depends on the maximum hardness of the steel material and P CM
It is known that they are inversely proportional to each other. Therefore 60
In order to ensure weld cracking resistance and susceptibility comparable to that of kg-class steel, it is necessary to ensure maximum hardness and P CM of 80 kg-class steel comparable to that of 60 kg-class steel. By the way, the maximum hardness of conventional 60 kg class steel is Hv360 or less.
Since P CM is 0.25 or less, in order to achieve the above objective, it is necessary to suppress the maximum hardness and P CM to the same level or lower than the above. On the other hand, maximum hardness is closely related to C content,
It is also known that in order to lower the maximum hardness, the C content can be reduced. For example, in Figure 1,
This is a graph showing the results of maximum hardness tests conducted on prototype steels with various C contents.From this result, in order to keep the maximum hardness below Hv360, the C content should be kept below 0.09%. I understand that. But C
If the content is reduced, the hardness of the steel material will inevitably decrease, so in order to maintain a high tensile strength of about 80 kg class, the amounts of other alloying elements must be increased. Based on the above knowledge, the present inventors have developed an 80 kg class high tensile strength steel that has a weld cracking susceptibility equal to or higher than that of 60 kg class high tensile strength steel, that is, the highest hardness steel.
With the goal of developing steel materials with Hv360 or less, P CM of 0.25% or less, and of course tensile strength of 80Kg/mm 2 or more, we first investigated the effects of alloying elements, especially B, on the hardenability of low carbon steel. We considered this. It is generally known that the hardenability multiple F B of B increases as the C content decreases, as shown in equation (A). F B = 1 + 1.5 (0.9 - C%) ... (A) However, these relationships have been confirmed only in regions where the amount of C exceeds 0.10%, and the incineration of B in the low C region below this has been confirmed. The incidence multiple has only been estimated. However, based on the results of geominy edge quenching tests conducted on steel materials with various C contents, the relationship between the C content and the hardenability multiple of B was determined, and the results showed the trends shown in Figure 2. In particular, it was found that the hardenability multiple of B in the region where the C content is 0.10% or less shows a value higher than the tendency estimated from the above equation (A) (dashed line in the figure), although there is considerable variation. . The reason why such a result was obtained is expected to be that in the low C region, the precipitation of the B-C compound is significantly delayed and the amount of precipitation at the γ grain boundaries is significantly reduced. However, as is clear from FIG. 2, the variation in the hardenability multiple of B is extremely large, so in order to reliably obtain the effect of B, it is necessary to reduce the variation as much as possible. Therefore, the present invention has proceeded with the study of specific measures to reduce the above-mentioned variations. When the hardenability multiple of B for materials with a C content of 0.10% or less was organized in relation to the N content, the results shown in Figure 3 were obtained, and by regulating the N content, A new fact was confirmed that the variation in the hardenability multiple of B becomes extremely small, and that the hardenability multiple improves significantly in the region where the N content is 40 PPm or less. The reason for this has not been completely elucidated, but in regions with low N content, the amount of BN and AlN precipitated at grain boundaries is small, and ferrite transformation during cooling is significantly delayed and martensite is formed. it is conceivable that. Incidentally, Al is a useful element as a deoxidizing and crystal grain adjusting element, but as the inventors have confirmed through experiments,
In addition to the above-mentioned effects, Al has an extremely important effect of stably securing the amount of solid solution B necessary for improving hardenability in relation to the B and N contents. In order to effectively exert these effects, at least
It was necessary to contain 0.04% or more. But Al
Even if the amount exceeds 0.10%, the above effects will reach a saturated state and will not improve any further.In fact, the amount of alumina-based inclusions will increase and the toughness and properties in the thickness direction will deteriorate significantly, so 0.10% It should be kept below. In addition, as mentioned above, Al has a close relationship with the N content that affects the hardenability multiple of B, and in order to ensure a satisfactory hardenability multiple, it is necessary to adjust the quenching temperature (T The components must be adjusted so that the Al content and N content in 〓) satisfy the above formula []. That is, in the present invention, N and Al in low C steel
It is possible to obtain 80kg-class high-strength steel with good hardenability by adjusting the content of Al to within a specified range and creating a certain relationship between the amount of Al and the amount of N at the quenching temperature. can. For example, Figure 4 shows the necessary range of Al and N content when the quenching temperature is 900°C, and the shaded range is essential for obtaining steel that meets the purpose of the present invention. It is a requirement. The quenching temperature can be determined appropriately depending on the composition of the steel material, but the most preferable temperature is (Ac 3 +50
The temperature is ℃). Next, we will provide a supplementary explanation of the reason for limiting the composition range of the steel material as described above. It is desirable that C be as small as possible from the viewpoint of weld hardenability, and in order to obtain the maximum hardness of Hv360 or less, it should be suppressed to 0.09% or less. However, in 80 kg class high-strength steel, when the C content is less than 0.04%,
Since it will not be possible to obtain the quenching hardness necessary to ensure a tensile strength of 80Kg/mm2 or more ,
% or more. In the case of this type of killed steel, Si is an element that is inevitably included in the deoxidation process, and also has the effect of increasing strength. However, too much content impairs weldability and toughness, so the upper limit was set at 0.55%. Mn is an essential element to ensure the strength and toughness required for 80 kg class high tensile strength steel, and in order to exhibit these effects significantly, Mn must be at least 0.6
% or more. However, if the Mn content is too high, problems will appear in terms of micro-segregation and weldability, so it should be kept below 1.4%. Cr has the effect of increasing hardenability, and has a value of 80Kg/mm 2
In order to secure tensile strength of at least
It is necessary to contain more than 0.3%. However, if it is too large, weldability deteriorates, so it must be kept below 1.0%. Mo has the effect of further increasing the hardenability of the steel material and the resistance to temper softening, and it is necessary to add more than 0.3% to ensure a tensile strength of 80 Kg/mm 2 or more. However, if it is contained in a large amount, the weld heat-affected zone will harden, the weld cracking resistance will deteriorate, and the cost will also increase, so it should be kept at 0.8% or less. When added in a small amount, V has the effect of increasing temper softening resistance and strength, but if it is added too much, the toughness will deteriorate significantly, so it should be kept at 0.1% or less. B has the effect of significantly increasing the hardenability of steel even when added in a very small amount, and in order to exhibit these effects significantly, it must be contained in an amount of 0.0005% or more.
However, if the content exceeds 0.002%, a large amount of B-C compounds will be generated at the austenite grain boundaries during quenching, resulting in deterioration of hardenability and toughness. Al should be in the range of 0.04-0.1% for the reasons detailed above. N is generally considered to be a harmful element for B-containing steel, but as mentioned above, in steel materials with a low N content of 0.004% or less, the hardenability factor of B is significantly improved. and
Even if it is less than 0.002%, hardenability will further improve due to the low N effect, but since the amount of AlN that contributes to the refinement of γ grains will be insufficient, the γ grains will become coarser and the toughness will decrease, so if it is contained at least 0.002% or more. It is necessary to do so. Cu has the effect of increasing strength when added in a small amount, but if it is added in excess of 0.5%, no further improvement in strength is seen, and on the contrary, it deteriorates weldability and surface quality, so it is less than 0.5%. should be stopped. Ni has the effect of increasing strength and toughness, but
Their effect reaches a saturation level at approximately 1.5%, and addition beyond that level is undesirable because it only increases cost. Note that P CM is used as an index for estimating the preheating temperature required to prevent weld cracking. For conventional 60 kg class high strength steel, this P CM is typically 0.25
% or less, and in order to improve the welding conditions of 80 kg class high tensile strength steel to the same level as 60 kg class steel, this P CM should be used.
It is necessary to keep it below 0.25%. As described above, in the present invention, the chemical components of 80 kg class high tensile strength steel, especially the content of N and B, the relationship between the content of N and Al at a given quenching temperature, and P CM etc. are adjusted appropriately. Therefore, it is possible to obtain a weld cracking susceptibility comparable to or exceeding that of 60 kg class high-strength steel, but even when using this steel, there are certain steps required to prevent weld cracking from occurring without preheating. It is necessary to use a coated arc welding rod having the following composition, and the final objective of the present invention can only be achieved by a combination of the two. That is, in the present invention, CaCO 3 40
~60%, CaF2 10~25%, Mn3~5%, Ni4~8
%, including Cr0.5~20%, Mo0.5~20% and 350
A low-hydrogen coated arc welding rod for high-strength steel must be used, in which a mild steel core is coated with a coating material that has a potential hydrogen content of 40 PPm or less in the temperature range of ~2000°C. The reason for the above numerical limitation is as follows. Ni has the effect of increasing the notch toughness of the weld metal and must be contained at least 4% or more.
Moreover, if it exceeds 8%, the toughness on the high temperature side decreases and weld cracking becomes more likely to occur, so it should be kept below this. If Mn is contained in an amount of 3% or more, it is effective as a deoxidizing agent and in improving the strength and toughness of the weld metal and in preventing hot cracking, but if it exceeds 5%, the toughness deteriorates and cold cracking becomes more likely to occur. Cr and Mo contribute to improving the strength of weld metal. Since the weld metal has a strength of 80 kg class, it is necessary to add 0.5% or more of each, but if too much, the toughness and cracking resistance tend to decrease.
% or less is preferable. Furthermore, what is extremely important in the present invention is that
Potential hydrogen content in the temperature range of 350 to 2000℃ (Generally, welding rods are dried at about 350℃,
This is the measured value of the amount of hydrogen generated when a dry welding rod is heated to a high temperature of 2000℃. )40PPm
This is something that must be done. That is, the present inventors used 80 kg class high-strength steel (steel shown in Table 1 A) that meets the requirements of the present invention as a base material, and recycled it at 350°C as a coating material for an 80 kg class low hydrogen-based coated arc welding rod. Items with different potential hydrogen amounts after drying ((2nd
JIS Z 3158 diagonal Y-shaped weld cracking test was conducted using (Table). Figure 5 shows the observation results of the root cracking rate at 25°C. As is clear from the results shown in Figure 5, the root cracking rate decreases rapidly when the potential hydrogen amount reaches a boundary of about 80 PPm, and becomes zero when the potential hydrogen amount becomes 40 PPm or less. From these results, in the present invention, it is essential to specify the type and content of elements contained in the coating material and to reduce the potential hydrogen amount to 40 PPm or less. As a means to reduce the amount of potential hydrogen in the coating material to 40 PPm or less, carefully select raw materials with low potential hydrogen (for example, raw materials that do not contain water of crystallization), raw materials with low hygroscopicity, and binders, and Examples include methods for appropriately controlling temperature and time. The present invention is roughly constructed as described above, and by using 80kg class high tensile strength steel with a specific composition and a specific 80kg class coated arc welding rod, no preheating is required as will be clear from the following examples. This makes it possible to perform welding without weld cracking, and provides an ideal technique for welding 80kg class high-strength steel. Next, examples of the present invention will be shown. Example 1 An 80 kg class steel plate having the composition shown in Table 1 was used as the base material, and a mild steel core wire was coated with a coating material having the composition shown in Table 2 (inventive bars 1 and 3, conventional bars 1 and 5). A diagonal Y-shaped welding cracking test was conducted in accordance with JIS Z 3158 using a coated arc welding rod made of the following materials. The results are summarized in Table 3.
【表】【table】
【表】【table】
【表】【table】
【表】【table】
【表】【table】
Claims (1)
0.55%以下、Mn:0.6〜1.4%、Cr:0.3%超1.0%
以下、Mo:0.3%超0.8%以下、V:0.1%以下、
B:0.0005〜0.0020%、Al:0.04〜0.1%及びN:
0.002〜0.004%を必須成分とし、残部が鉄及び不
可避不純物であり、且つ下記〔〕式で算出され
るPCMが0.25%以下であると共に、焼入温度(T
〓)におけるAl量とN量の関係が下記〔〕式
を満足する鋼を焼入・焼戻処理してなる引張強さ
80Kg/mm2以上の耐溶接割れ感受性の優れた80Kg/
mm2級高張力鋼を母材とし、 〔〕…PCM=C(%)+1/30Si(%)+1/20Mn
(%)+1/20Cu(%) +1/60Ni(%)+1/20Cr(%)+1/15Mo(%) +1/10V(%)+5B(%) 下記組成即ち、 CaCO340〜60%、CaF210〜25%、Mn3〜5%、
Ni4〜8%、Cr0.5〜2.0%、Mo0.5〜2.0%を含む
と共に、350〜2000℃におけるポテンシヤル水素
量が40PPm以下である被覆剤を軟鋼心線に被覆
してなる高張力鋼用低水素系被覆アーク溶接棒を
使用して、前記母材を溶接することを特徴とする
高張力鋼の溶接方法。 2 C:0.04〜0.09%(重量%:以下同様)、Si:
0.55%以下、Mn:0.6〜1.4%、Cr:0.3%超1.0%
以下、Mo:0.3%超0.8%以下、V:0.1%以下、
B:0.0005〜0.002%、Al:0.04〜0.1%及びN:
0.002〜0.004%を必須成分とするほか、Cu:0.5
%以下及び/若しくはNi:1.5%以下を含有し、
更に残部が鉄及び不可避不純物であり、且つ下記
〔〕式で算出されるPCMが0.25%以下であると共
に、焼入温度(T〓)におけるAl量とN量の関
係が下記〔〕式を満足する鋼を、焼入・焼戻処
理して得られる引張強さ80Kg/mm2以上の強度を有
する耐溶接割れ感受性の優れた80Kg/mm2級高張力
鋼を母材とし、 〔〕…PCM=C(%)+1/30Si(%)+1/20Mn
(%)+1/20Cu(%) +1/60Ni(%)+1/20Cr(%)+1/15Mo(%) +1/10V(%)+5B(%) 下記組成即ち、 CaCO340〜60%、CaF210〜25%、Mn3〜5%、
Ni4〜8%、Cr0.5〜2.0%、Mo0.5〜2.0%を含む
と共に、350〜2000℃におけるポテンシヤル水素
量が40PPm以下である被覆剤を軟鋼心線に被覆
してなる高張力鋼用低水素系被覆アーク溶接棒を
使用して、前記母材を溶接することを特徴とする
高張力鋼の溶接方法。[Claims] 1 C: 0.04 to 0.09% (weight %: the same applies hereinafter), Si:
0.55% or less, Mn: 0.6-1.4%, Cr: over 0.3% 1.0%
Below, Mo: more than 0.3% and 0.8% or less, V: 0.1% or less,
B: 0.0005-0.0020%, Al: 0.04-0.1% and N:
0.002 to 0.004% is an essential component, the remainder is iron and unavoidable impurities, and P CM calculated by the following formula [] is 0.25% or less, and the quenching temperature (T
Tensile strength obtained by quenching and tempering steel whose relationship between Al content and N content in 〓) satisfies the following formula []
80Kg/mm 2 or more with excellent weld cracking resistance and susceptibility
mm Class 2 high tensile strength steel is used as the base material, []...P CM = C (%) + 1/30Si (%) + 1/20Mn
(%) +1/20Cu (%) +1/60Ni (%) +1/20Cr (%) +1/15Mo (%) +1/10V (%) +5B (%) The following composition: CaCO 3 40-60%, CaF 2 10-25%, Mn 3-5%,
For high-strength steel made by coating a mild steel core with a coating material containing 4 to 8% Ni, 0.5 to 2.0% Cr, and 0.5 to 2.0% Mo, and having a potential hydrogen content of 40 PPm or less at 350 to 2000°C. A method for welding high-strength steel, the method comprising welding the base metal using a low-hydrogen coated arc welding rod. 2 C: 0.04 to 0.09% (weight%: the same applies below), Si:
0.55% or less, Mn: 0.6-1.4%, Cr: over 0.3% 1.0%
Below, Mo: more than 0.3% and 0.8% or less, V: 0.1% or less,
B: 0.0005-0.002%, Al: 0.04-0.1% and N:
In addition to 0.002-0.004% as an essential component, Cu: 0.5
% or less and/or Ni: 1.5% or less,
Furthermore, the remainder is iron and unavoidable impurities, P CM calculated by the following formula [] is 0.25% or less, and the relationship between the amount of Al and the amount of N at the quenching temperature (T〓) satisfies the formula [] below. The base material is 80Kg/mm class 2 high tensile strength steel, which has a tensile strength of 80Kg/mm2 or more and has excellent weld cracking resistance and susceptibility, obtained by quenching and tempering the steel that satisfies the requirements []... P CM = C (%) + 1/30Si (%) + 1/20Mn
(%) +1/20Cu (%) +1/60Ni (%) +1/20Cr (%) +1/15Mo (%) +1/10V (%) +5B (%) The following composition: CaCO 3 40-60%, CaF 2 10-25%, Mn 3-5%,
For high-strength steel made by coating a mild steel core with a coating material containing 4 to 8% Ni, 0.5 to 2.0% Cr, and 0.5 to 2.0% Mo, and having a potential hydrogen content of 40 PPm or less at 350 to 2000°C. A method for welding high-strength steel, the method comprising welding the base metal using a low-hydrogen coated arc welding rod.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8892679A JPS5614085A (en) | 1979-07-12 | 1979-07-12 | Welding method of high tensile steel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP8892679A JPS5614085A (en) | 1979-07-12 | 1979-07-12 | Welding method of high tensile steel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5614085A JPS5614085A (en) | 1981-02-10 |
| JPH0126797B2 true JPH0126797B2 (en) | 1989-05-25 |
Family
ID=13956506
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP8892679A Granted JPS5614085A (en) | 1979-07-12 | 1979-07-12 | Welding method of high tensile steel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5614085A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS55122726A (en) * | 1979-03-16 | 1980-09-20 | Asahi Chem Ind Co Ltd | Prolonged release drug composition |
Family Cites Families (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5852758B2 (en) * | 1974-10-04 | 1983-11-25 | 新日本製鐵株式会社 | Low hydrogen coated arc welding rod for high tensile strength steel |
| JPS527320A (en) * | 1975-07-08 | 1977-01-20 | Nippon Steel Corp | High tension steel of greatly reduced hardening property suitable for 80k joule/cm heat input welding |
-
1979
- 1979-07-12 JP JP8892679A patent/JPS5614085A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5614085A (en) | 1981-02-10 |
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