JPH04367393A - Low hydrogen type coated electrode - Google Patents

Low hydrogen type coated electrode

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Publication number
JPH04367393A
JPH04367393A JP20250191A JP20250191A JPH04367393A JP H04367393 A JPH04367393 A JP H04367393A JP 20250191 A JP20250191 A JP 20250191A JP 20250191 A JP20250191 A JP 20250191A JP H04367393 A JPH04367393 A JP H04367393A
Authority
JP
Japan
Prior art keywords
caf2
welding
clock
caco3
bead
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.)
Pending
Application number
JP20250191A
Other languages
Japanese (ja)
Inventor
Takashi Wada
俊 和田
Tomoyuki Abe
阿部知之
Shozo Naruse
成瀬省三
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Kobe Steel Ltd
Original Assignee
Kobe Steel Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Kobe Steel Ltd filed Critical Kobe Steel Ltd
Priority to JP20250191A priority Critical patent/JPH04367393A/en
Publication of JPH04367393A publication Critical patent/JPH04367393A/en
Pending legal-status Critical Current

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Abstract

PURPOSE:To provide the low hydrogen type coated electrode which allows downward welding even in welding in all positions and allows the enhancement of performance in downward welding of the circumferential butt joint of a pipe in particular. CONSTITUTION:This low hydrogen type coated electrode is constituted by coating the outer periphery of a steel core wire with a coating material contg. 35 to 55% CaCO3, 1 to 4% SrCO3, 1.5 to 4% CaF2, 1 to 5% TiO2, 5 to 12% SiO2, 3 to 9% Si, 1 to 6% Mn, and 15 to 40% Fe, and satisfying the relations 9 to 25 CaCO3/CaF2, and 5 to 22 Fe/CaF2. The effect of an extremely easy performability of the welding operation is obtd. without requiring the welding technique of a high degree if 0.5 to 3% Ti and 0.05 to 0.2% B are further incorporated into this coating material. Further, the toughness of the ferrite structure is increased and the low-temp. toughness is improved even for the additional requirement for the low-temp. toughness if 0.5 to 4.5% Ni is incorporated therein.

Description

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

【0001】0001

【産業上の利用分野】本発明は、低水素系被覆アーク溶
接棒に関し、特にパイプの円周突合せ継手の下進溶接に
適用して優れた効果を発揮するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a low-hydrogen coated arc welding rod, and is particularly effective when applied to downward welding of circumferential butt joints of pipes.

【0002】0002

【従来の技術】従来より、パイプラインの現場における
円周突合せ溶接は、国内では低水素系被覆アーク溶接棒
やイルミナイト系被覆アーク溶接棒を用いた上進溶接が
行われており、一方、外国ではハイセルロース系被覆ア
ーク溶接棒を用いた下進溶接が行なわれている。しかし
、高張力鋼管の溶接、特に寒冷地における現場溶接では
水素による割れが大きな問題となることから、低水素系
被覆アーク溶接棒の使用が望ましいものの、従来、低水
素系被覆アーク溶接棒では下進で溶接することが非常に
困難であった。
[Prior Art] Traditionally, circumferential butt welding at pipeline sites has been carried out in Japan by upward welding using low-hydrogen coated arc welding rods or illuminite coated arc welding rods; In other countries, downward welding is performed using high-cellulose coated arc welding rods. However, when welding high-strength steel pipes, especially on-site welding in cold regions, hydrogen-induced cracking is a major problem, so it is desirable to use a low-hydrogen coated arc welding rod. It was very difficult to weld in advance.

【0003】0003

【発明が解決しようとする課題】この問題を解決するた
め、本件出願人は先に特公昭56−21519号を提案
した。しかし、上記提案の低水素系被覆アーク溶接棒は
、それ以前のものに比較すると格段に優れた性能を有す
るものであるが、最近、より高能率化、苛酷な性能が求
められるようになり、必ずしも満足し得るものではなく
、改善が求められていた。
[Problem to be Solved by the Invention] In order to solve this problem, the applicant of the present invention previously proposed Japanese Patent Publication No. 56-21519. However, although the low hydrogen-based coated arc welding rod proposed above has much superior performance compared to previous ones, recently there has been a demand for higher efficiency and harsher performance. This was not necessarily satisfactory, and improvements were required.

【0004】すなわち、パイプの円周突合せ継手の下進
溶接において、図1に示すように4.5時〜6時(7.
5時〜6時)の位置を溶接する際、ビードと母材とのな
じみが不十分となることがあり、手直し作業(グライン
ダ作業等)が必要であった。
That is, in downward welding of circumferential butt joints of pipes, as shown in FIG.
When welding at the position (from 5 o'clock to 6 o'clock), the bead and the base metal may not fit together sufficiently, and rework (such as grinding work) is required.

【0005】本発明は、かゝる要請に応えるべくなされ
たものであって、特にパイプの円周突合せ継手の下進溶
接において4.5時〜6時(7.5時〜6時)の位置で
の溶接のみならず、全姿勢での溶接においても下進溶接
が可能であり、しかも高能率化も可能な低水素系被覆ア
ーク溶接棒を提供することを目的とするものである。
[0005] The present invention has been made in response to such demands, and is particularly suitable for downward welding of circumferential butt joints of pipes between 4.5 o'clock and 6 o'clock (7.5 o'clock - 6 o'clock). The object of the present invention is to provide a low-hydrogen-based coated arc welding rod that is capable of downward welding not only in position but also in all positions, and that can also be highly efficient.

【0006】[0006]

【課題を解決するための手段】前記課題を解決するため
、本発明者等は、高能率化と共に、特定の溶接位置(4
.5時〜6時、7.5時〜6時)において、ビードと母
材とのなじみが悪くなるのを防ぎ得る方策について種々
検討を重ねた結果、ここに本発明をなしたものである。
[Means for Solving the Problems] In order to solve the above-mentioned problems, the inventors of the present invention have developed a method for achieving high efficiency and a specific welding position (4
.. 5:00 to 6:00 and 7.5:00 to 6:00), the present invention was developed as a result of various studies on ways to prevent the bead from becoming poorly compatible with the base material.

【0007】すなわち、本発明(第1発明)は、CaC
O3:35〜55%、SrCO3:1〜4%、CaF2
:1.5〜4%、TiO2:1〜5%、SiO2:5〜
12%、Si:3〜9%、Mn:1〜6%及びFe:1
5〜40%を含有し、かつ、CaCO3/CaF2:9
〜25、Fe/CaF2:5〜22の関係を満たす被覆
剤を鋼心線外周に塗布してなることを特徴とする低水素
系被覆アーク溶接棒を要旨とするものである。
[0007] That is, the present invention (first invention)
O3: 35-55%, SrCO3: 1-4%, CaF2
: 1.5~4%, TiO2: 1~5%, SiO2: 5~
12%, Si: 3-9%, Mn: 1-6% and Fe: 1
Contains 5-40% and CaCO3/CaF2:9
~25, Fe/CaF2: The gist of the present invention is a low hydrogen-based coated arc welding rod characterized by coating the outer periphery of a steel core wire with a coating agent satisfying the relationship of 5 to 22.

【0008】また、他の本発明(第2発明)は、CaC
O3:35〜55%、SrCO3:1〜4%、CaF2
:1.5〜4%、TiO2:1〜5%、SiO2:5〜
12%、Si:3〜9%、Mn:1〜6%及びFe:1
5〜40%を含有し、更にTi:0.5〜3%及びB:
0.05〜0.2%を含有し、かつ、CaCO3/Ca
F2:9〜25、Fe/CaF2:5〜22の関係を満
たす被覆剤を鋼心線外周に塗布してなることを特徴とす
る低水素系被覆アーク溶接棒を要旨とするものである。
[0008] Another present invention (second invention) is that CaC
O3: 35-55%, SrCO3: 1-4%, CaF2
: 1.5~4%, TiO2: 1~5%, SiO2: 5~
12%, Si: 3-9%, Mn: 1-6% and Fe: 1
Contains 5 to 40%, furthermore Ti: 0.5 to 3% and B:
Contains 0.05-0.2%, and CaCO3/Ca
The gist of the present invention is a low hydrogen-based coated arc welding rod characterized by coating the outer periphery of a steel core wire with a coating material satisfying the relationships of F2: 9 to 25 and Fe/CaF2: 5 to 22.

【0009】また、更に他の本発明(第3発明)は、第
2発明において被覆剤が更にNi:0.5〜4.5%を
含有していることを特徴とするものである。
[0009] Still another aspect of the invention (third invention) is characterized in that the coating material in the second invention further contains Ni: 0.5 to 4.5%.

【0010】以下に本発明を更に詳述する。The present invention will be explained in more detail below.

【0011】[0011]

【作用】[Effect]

【0012】各本発明は前述の構成を有する低水素系被
覆アーク溶接棒であるが、第1発明によれば、特にパイ
プの円周突合せ継手においても下進溶接が可能であり、
しかも高能率化も可能な低水素系被覆アーク溶接棒を提
供することができる。
[0012] Each of the present inventions is a low hydrogen-based coated arc welding rod having the above-mentioned configuration, and according to the first invention, downward welding is possible especially in circumferential butt joints of pipes,
Furthermore, it is possible to provide a low hydrogen-based coated arc welding rod that can also be highly efficient.

【0013】一方、第2発明及び第3発明は、溶接オペ
レータの高齢化や、溶接作業性をより容易にし、負荷を
軽減したいとの要請が強まり、更に溶接作業性に優れた
低水素系被覆アーク溶接棒が望まれるようになり、特に
溶接作業性のなかでアークの集中性は安定した溶け込み
を得るのに必要であり、またビードと母材のなじみも従
来に増して良好なことが望まれるようになってきたこと
に鑑みて、特定の溶接位置(4.5時〜6時、7.5時
〜6時)において、ビードと母材とのなじみが悪くなる
のを防ぎ得る方策を勘案しつつ、更に全姿勢でのアーク
の集中性及び母材とのなじみを改善する点について種々
検討を重ねた結果、完成したものである。
On the other hand, the second and third inventions are directed to the aging of welding operators and the increasing demand for easier welding workability and lightening of the load. Arc welding rods have come to be desired, especially in terms of welding workability, arc concentration is necessary to obtain stable penetration, and it is desirable that the bead and base metal fit better than ever before. In light of this, we have developed measures to prevent the bead and base metal from becoming poorly compatible at specific welding positions (4.5 o'clock to 6 o'clock, 7.5 o'clock to 6 o'clock). With this in mind, we conducted various studies to improve arc concentration in all positions and compatibility with the base material, resulting in the completion of this work.

【0014】さて、本発明における被覆剤成分の特徴の
一つは、高能率化のために、Feを必須成分として添加
したことであり、その量も前記提案の低水素系被覆アー
ク溶接棒の場合よりも相当多く添加している。しかし、
Feの添加は高能率化を意図したものであるが、この多
量添加による高能率化がビードと母材のなじみに悪影響
を与える一因になっていることが判明した。
Now, one of the characteristics of the coating material component in the present invention is that Fe is added as an essential component in order to improve efficiency, and the amount of Fe is also the same as that of the low-hydrogen coated arc welding rod proposed above. Much more was added than in the case. but,
Although the addition of Fe was intended to increase efficiency, it was found that the increase in efficiency due to the addition of a large amount of Fe was a factor that adversely affected the compatibility between the bead and the base material.

【0015】そこで、この問題を解決するために、本発
明では、次のような基本的な手段をとることにより、全
姿勢でのビードと母材のなじみを飛躍的に改善したもの
である。
In order to solve this problem, the present invention takes the following basic measures to dramatically improve the fit between the bead and the base material in all positions.

【0016】(イ)CaF2の添加量を少なくすること
。 (ロ)CaCO3/CaF2の比を大きくすること。 (ハ)Fe/CaF2の比を特定すること。 (ニ)必要に応じてTiとBを添加したこと。 (ホ)衝撃性能を更に向上させたいときにNiを添加し
たこと。
(a) Reduce the amount of CaF2 added. (b) Increasing the ratio of CaCO3/CaF2. (c) Specifying the Fe/CaF2 ratio. (d) Ti and B were added as necessary. (e) Ni was added when it was desired to further improve impact performance.

【0017】次に本発明における被覆剤の成分限定理由
を説明する。
Next, the reasons for limiting the components of the coating material in the present invention will be explained.

【0018】(CaCO3:35〜55%)CaCO3
はガス発生剤として添加するが、35%未満ではガス発
生量が少なくシールド不足になると共にスラグの粘性が
小さくなってビード表面にピットが発生し、また2時〜
4時の位置でのビードのなじみが悪くなる。一方、55
%を超えるとスラグの粘性が著しく増大してビードのな
じみが悪くなり、またガス発生量が多くなってスパッタ
の発生が多くなる。したがって、CaCO3量は35〜
55%の範囲とする。
(CaCO3: 35-55%) CaCO3
is added as a gas generating agent, but if it is less than 35%, the amount of gas generated is small and shielding is insufficient, the viscosity of the slag is reduced, and pits are formed on the bead surface.
The bead does not fit well at the 4 o'clock position. On the other hand, 55
If it exceeds %, the viscosity of the slag will increase significantly, resulting in poor bead compatibility, and the amount of gas generated will increase, resulting in increased spatter. Therefore, the amount of CaCO3 is 35~
The range is 55%.

【0019】(SrCO3:1〜4%)SrCO3はク
レータの拡がりを大きくし、またビードのなじみを良好
にする作用がある。しかし、1%未満ではその効果がな
く、また4%を超えるとアークが不安定となってスパッ
タが増加し、またスラグの剥離性が悪くなる。したがっ
て、SrCO3量は1〜4%の範囲とする。
(SrCO3: 1 to 4%) SrCO3 has the effect of increasing the spread of the crater and improving the conformability of the bead. However, if it is less than 1%, there is no effect, and if it exceeds 4%, the arc becomes unstable, spatter increases, and the slag releasability deteriorates. Therefore, the amount of SrCO3 is set in the range of 1 to 4%.

【0020】(CaF2:1.5〜4%)CaF2はス
ラグの粘性と流動性を調整する作用がある。しかし、1
.5%未満ではその効果がなく、これより多くすると2
時〜4時の位置で良好なビードが形成されるが、4%を
超えるとスラグの粘性が比較的小さくなりスラグの流動
性が増して、4.5時〜6時及び7.5時〜6時の位置
においてビードと母材のなじみが悪くなる。したがって
、CaF2量は1.5〜4%の範囲とする。
(CaF2: 1.5-4%) CaF2 has the effect of adjusting the viscosity and fluidity of the slag. However, 1
.. Less than 5% has no effect, and more than 2%
A good bead is formed between 4:00 and 4:00, but when it exceeds 4%, the viscosity of the slag becomes relatively small and the fluidity of the slag increases. At the 6 o'clock position, the bead and base metal do not fit well. Therefore, the amount of CaF2 is set in the range of 1.5 to 4%.

【0021】(TiO2:1〜5%、SiO2:5〜1
2%)TiO2、SiO2はそれぞれスラグ形成剤とし
て添加するが、TiO2が1%未満ではビードのなじみ
が悪くなり、また5%を超えるとスラグの流動性が増し
て2時〜4時の位置でスラグが垂れ落ち易くなる。Si
O2が5%未満ではアークが弱くクレーターの拡がりも
小さく2時〜4時の位置でのビードのなじみが悪くなり
易く、また12%を超えると特に2時〜4時の位置でス
ラグが邪魔し巻き込み易く良好なビードが得られなくな
る。したがって、TiO2量は1〜5%の範囲とし、S
iO2量は5〜12%の範囲とする。なお、TiO2は
ルチール、イルメナイトとして、SiO2は硅酸塩や硅
砂として添加すればよい。
(TiO2: 1-5%, SiO2: 5-1
2%) TiO2 and SiO2 are each added as a slag forming agent, but if TiO2 is less than 1%, the bead will not fit well, and if it exceeds 5%, the fluidity of the slag will increase and Slag easily drips down. Si
If the O2 content is less than 5%, the arc will be weak and the crater will not spread too much, making it difficult for the bead to fit in between the 2 o'clock and 4 o'clock positions.If the O2 content exceeds 12%, the slag will get in the way, especially at the 2 o'clock to 4 o'clock positions. It is easy to get rolled up, making it impossible to obtain a good bead. Therefore, the amount of TiO2 should be in the range of 1 to 5%, and the amount of S
The amount of iO2 is in the range of 5 to 12%. Note that TiO2 may be added as rutile or ilmenite, and SiO2 may be added as silicate or silica sand.

【0022】(Si:3〜9%、Mn:1〜6%)Si
、Mnは脱酸剤として添加されるが、それぞれ下限値未
満ではその効果がなく、また上限値を超えると脱酸過剰
となってビード表面にピットが発生するようになる。な
お、Siは単体或いはFe−Si、Si−Mn、Ca−
Si等の形で添加できる。Mnは金属Mn或いはFe−
Mn、Si−Mn等の形で添加できる。
(Si: 3-9%, Mn: 1-6%) Si
, Mn are added as deoxidizing agents, but if they are below the lower limit, they have no effect, and if they exceed the upper limit, excessive deoxidation occurs and pits are generated on the bead surface. In addition, Si is a simple substance or Fe-Si, Si-Mn, Ca-
It can be added in the form of Si, etc. Mn is metal Mn or Fe-
It can be added in the form of Mn, Si-Mn, etc.

【0023】(CaCO3/CaF2:9〜25)Ca
CO3/CaF2の比は、スラグの粘性及び流動性に大
きな影響を及ぼし、全姿勢の下進溶接では重要な因子で
ある。この比が9未満ではスラグの粘性が比較的小さく
なり、4.5時〜6時(7.5〜6時)の位置での作業
性が悪く、この比を大きくしていくと、2時〜4時の位
置での作業性が良くなるが、25を超えるとスラグの粘
性が増して4.5時〜6時(7.5〜6時)の位置での
作業性が劣り、ビードと母材のなじみが悪くなる。した
がつて、CaCO3/CaF2の比は9〜25の範囲と
する。
(CaCO3/CaF2:9-25)Ca
The CO3/CaF2 ratio has a great effect on slag viscosity and fluidity and is an important factor in all-position downward welding. If this ratio is less than 9, the viscosity of the slag will be relatively small, and workability at the 4.5 o'clock to 6 o'clock (7.5 to 6 o'clock) positions will be poor. The workability at the ~4 o'clock position is better, but if it exceeds 25, the viscosity of the slag increases and the workability at the 4.5 o'clock to 6 o'clock (7.5 to 6 o'clock) position is poor, and the bead and Compatibility with the base material deteriorates. Therefore, the CaCO3/CaF2 ratio should be in the range of 9-25.

【0024】(Fe:15〜40%)Feは溶着効率を
向上させるために添加するが、15%未満ではその効果
が少なく、40%を超えると相対的にスラグ形成剤の量
が少なくなり、スラグの被包性が悪くなる。したがって
、Fe量は15〜40%の範囲とする。
(Fe: 15-40%) Fe is added to improve welding efficiency, but if it is less than 15%, the effect will be small, and if it exceeds 40%, the amount of slag forming agent will be relatively small. Slag encapsulation deteriorates. Therefore, the amount of Fe is in the range of 15 to 40%.

【0025】(Fe/CaF2:5〜22)上述の如く
溶着効率を向上させるためにFeを比較的多量に添加す
ると、高能率溶接が可能となるが、一方では4.5時〜
6時の位置及び7.5時〜6時の位置においてビードと
母材のなじみを悪くする一因となる。これを防止するた
めにはFe/CaF2の比を5以上とすればよいことが
判明した。この比が5未満では特に溶融金属がたれ易く
なり、前記位置でのビードと母材のなじみが改善されな
い。また、この比が22を超えるとクレーターの拡がり
が悪くなる。したがって、Fe/CaF2の比は5〜2
2の範囲とする。
(Fe/CaF2: 5-22) As mentioned above, when a relatively large amount of Fe is added to improve the welding efficiency, high efficiency welding becomes possible;
This contributes to poor compatibility between the bead and the base material at the 6 o'clock position and the 7.5 o'clock to 6 o'clock positions. It has been found that in order to prevent this, the Fe/CaF2 ratio should be set to 5 or more. If this ratio is less than 5, the molten metal tends to sag, and the fit between the bead and the base material at the above-mentioned positions is not improved. Moreover, if this ratio exceeds 22, the spread of the crater becomes worse. Therefore, the ratio of Fe/CaF2 is 5-2
The range shall be 2.

【0026】(Ti:0.5〜3%)Tiの溶接作業性
に与える作用としては、アークの集中性を改善し、かつ
アークをソフトにすることができるが、0.5%未満で
はアークの集中性が劣るので融合不良の発生原因となる
ので運棒操作に熟練を要する。また3%を超えるとアー
クが弱くなりすぎて溶け込み不良が発生する。したがっ
て、Ti量は0.5〜3%の範囲とする。
(Ti: 0.5-3%) The effect of Ti on welding workability is that it can improve arc concentration and soften the arc, but if it is less than 0.5%, the arc Since the concentration of the stick is poor, it causes poor fusion, and requires skill in operating the stick. If it exceeds 3%, the arc becomes too weak and poor penetration occurs. Therefore, the amount of Ti is set in the range of 0.5 to 3%.

【0027】(B:0.05〜0.2%)Bは母材との
なじみを改善するために有効であるが、0.05%以下
では母材とのなじみが劣るのでなじみ不足の発生原因と
なり、運棒操作に熟練を要する。また0.2%を超える
とアークが弱くなりすぎ、溶け込み不良が発生する。し
たがって、B量は0.05〜0.2%の範囲とする。
(B: 0.05-0.2%) B is effective for improving the compatibility with the base material, but if it is less than 0.05%, the compatibility with the base material is poor, resulting in insufficient compatibility. This causes the problem and requires skill to operate the stick. Moreover, if it exceeds 0.2%, the arc becomes too weak and poor penetration occurs. Therefore, the amount of B is set in the range of 0.05 to 0.2%.

【0028】(Ni:0.5〜4.5%)Niはフェラ
イト組織の強靱化を図るのに有効であるが、0.5%未
満ではその効果が得られず、一方、4.5%を超えると
アークが弱くなり溶滴移行性が悪くなって溶け込み不良
が発生する。したがって、Ni量は0.5〜4.5%の
範囲とする。
(Ni: 0.5-4.5%) Ni is effective in strengthening the ferrite structure, but if it is less than 0.5%, the effect cannot be obtained; If it exceeds this value, the arc becomes weaker, droplet migration becomes worse, and poor penetration occurs. Therefore, the amount of Ni is set in the range of 0.5 to 4.5%.

【0029】なお、溶着金属の機械的性質を調整するた
めにCr、Mo、Cu、Nb等の合金成分を1種類以上
を同時に添加してもよい。
[0029] In order to adjust the mechanical properties of the weld metal, one or more alloy components such as Cr, Mo, Cu, and Nb may be added at the same time.

【0030】また、本発明では通常粘結剤として水ガラ
スを使用するが、水ガラスにはNa2O、K2O等の成
分が若干量含まれているので、スラグ形成剤、アーク安
定剤としても作用する。本発明における被覆剤と鋼心線
の断面積比は適宜決定されるものである。
[0030] Also, in the present invention, water glass is normally used as a binder, but since water glass contains a small amount of components such as Na2O and K2O, it also acts as a slag forming agent and an arc stabilizer. . The cross-sectional area ratio between the coating material and the steel core wire in the present invention is determined as appropriate.

【0031】次に本発明の実施例を示す。Next, examples of the present invention will be shown.

【0032】[0032]

【実施例1】鋼心線に[Example 1] Steel core wire

【表1】 に示す成分組成の被覆剤を塗布して、試験溶接棒を試作
した。これらの試験溶接棒を使用し、水平固定管(10
.3mmt×1016mmφ)の突合せ継手(60°V
開先)を下進で溶接し、各溶接位置における作業性を調
査した。 その結果を
[Table 1] A test welding rod was prepared by applying a coating having the composition shown in Table 1. Using these test welding rods, a horizontal fixed pipe (10
.. 3mmt×1016mmφ) butt joint (60°V
The workability at each welding position was investigated by welding the groove in a downward direction. The result

【表2】 に併記する。[Table 2] Also listed in

【0033】表2より明らかなように、本発明例はいず
れも、どの位置の下進溶接においても優れた溶接性を示
している。
As is clear from Table 2, all of the examples of the present invention exhibit excellent weldability in downward welding at any position.

【0034】一方、比較例No.11はCaCO3が少
ないので3時(9時)の位置でのビードのなじみが悪く
、またCaCO3/CaF2比が小さいので6時の位置
でのビードのなじみがやや悪い。
On the other hand, comparative example No. No. 11 has a low amount of CaCO3, so the bead does not fit well at the 3 o'clock (9 o'clock) position, and the CaCO3/CaF2 ratio is small, so the bead does not fit well at the 6 o'clock position.

【0035】比較例No.12はCaCO3/CaF2
比が大きすぎるので6時の位置でのビードのなじみが悪
い。
Comparative Example No. 12 is CaCO3/CaF2
Because the ratio is too large, the bead does not fit well at the 6 o'clock position.

【0036】比較例No.13は、CaF2が少ないの
で、CaCO3/CaF2の比及びFe/CaF2の比
が大きくなりすぎ、スラグの安定性及びビードのなじみ
が悪い。しかもSrCO3が多いのでスラグの剥離性も
悪くなっている。
Comparative Example No. No. 13 has a small amount of CaF2, so the ratio of CaCO3/CaF2 and the ratio of Fe/CaF2 becomes too large, resulting in poor slag stability and bead conformability. Furthermore, since the amount of SrCO3 is large, the slag releasability is also poor.

【0037】比較例No.14はSrCO3及びTiO
2が低いのでビードのなじみが悪い。しかもFeが高い
のでスラグの被包性が悪い。また、Siが低いのでブロ
ーホールが発生した。
Comparative Example No. 14 is SrCO3 and TiO
2 is low, so the bead does not fit well. Moreover, since the Fe content is high, the slag encapsulation property is poor. In addition, blowholes occurred due to the low Si content.

【0038】比較例No.15はSiO2が低いのでア
ークがやや弱く、またFe/CaF2の比が低いので6
時の位置でビードが垂れ易くなり、なじみが悪い。
Comparative Example No. 15 has a low SiO2, so the arc is a little weak, and the Fe/CaF2 ratio is low, so 6
The bead tends to sag at the time position, making it difficult to blend in.

【0039】比較例No.16はTiO2が多いので3
時(9時)の位置でのスラグ安定性が悪くビードのなじ
みがやや悪い。
Comparative Example No. 16 has a lot of TiO2, so 3
The slug stability at the 9 o'clock position is poor, and the bead does not fit in well.

【0040】比較例No.17はCaCO3が少ないの
で3時(9時)の位置や6時の位置でのビードのなじみ
がやや悪い。
Comparative Example No. No. 17 has less CaCO3, so the bead conformability at the 3 o'clock (9 o'clock) and 6 o'clock positions is somewhat poor.

【0041】比較例No.18はSiO2が多いのでス
ラグが邪魔し易く、しかもFe/CaF2比が小さいの
で3時(9時)〜6時の位置でのビードのなじみが悪い
Comparative Example No. No. 18 has a large amount of SiO2, so the slag easily gets in the way, and the Fe/CaF2 ratio is small, so the bead does not conform well at the 3 o'clock (9 o'clock) to 6 o'clock positions.

【0042】比較例No.19はスラグ安定性やビード
のなじみは良いものの、脱酸剤が多すぎるため、ビード
表面にピットが発生した。
Comparative Example No. Although No. 19 had good slag stability and bead conformability, pits were generated on the bead surface because there was too much deoxidizing agent.

【0043】比較例No.20はSiO2が低いのでア
ークはやや弱く、3時(9時)の位置でのビードのなじ
みがやや悪い。また、Siが高いので脱酸過剰となり、
ビード表面にピットが発生した。
Comparative Example No. No. 20 has a low SiO2 content, so the arc is a little weak, and the bead conformation at the 3 o'clock (9 o'clock) position is a little bad. In addition, due to high Si content, excessive deoxidation occurs,
Pit occurred on the bead surface.

【0044】比較例No.21はMnが少ないため脱酸
不足し、ブローホールが発生した。
Comparative Example No. In No. 21, deoxidation was insufficient due to low Mn content, and blowholes occurred.

【0045】[0045]

【実施例2】鋼心線に[Example 2] Steel core wire

【表3】 、[Table 3] ,

【表4】 に示す成分組成の被覆剤を塗布して、試験溶接棒を試作
した。これらの試験溶接棒を使用し、水平固定管(12
mmt×1000mmφ)の突合せ継手(60°V開先
)を下進で溶接し、各溶接位置における作業性並びに靭
性を調査した。衝撃試験には図2に示す位置から採取し
た衝撃試験片(10mmt×10mmw×50mml、
2Vノッチ)を用いた。それらの結果を
[Table 4] A test welding rod was prepared by applying a coating having the composition shown in Table 4. Using these test welding rods, a horizontal fixed pipe (12
mmt×1000 mmφ) butt joints (60° V groove) were welded in a downward direction, and the workability and toughness at each welding position were investigated. For the impact test, impact test pieces (10mmt x 10mmw x 50mml,
2V notch) was used. those results

【表5】 、[Table 5] ,

【表6】 に併記する。[Table 6] Also listed in

【0046】表5、表6より明らかなように、本発明例
はいずれも、どの位置の下進溶接においても特に優れた
溶接作業性を示している。
As is clear from Tables 5 and 6, all of the examples of the present invention exhibit particularly excellent welding workability in downward welding at any position.

【0047】一方、比較例No.13は、Tiが少ない
ため、アークの集中性が劣るので溶接作業者に高度な溶
接技術が要求される。
On the other hand, Comparative Example No. In No. 13, the concentration of the arc is poor due to the small amount of Ti, so the welding operator is required to have advanced welding techniques.

【0048】比較例No.14は、Bが少ないため、母
材とのなじみが劣るので溶接作業者に高度な溶接技術が
要求される。
Comparative Example No. Since No. 14 has a small amount of B, it has poor compatibility with the base metal, and requires advanced welding techniques from the welding operator.

【0049】比較例No.15は、CaCO3及びSi
O2が少なく、Ti及びBが多く、しかもCaCO3/
CaF2の比が小さいため、アークが弱くなりすぎ、ク
レータの拡がりがなく、スラグが邪魔し易くなり、母材
とのなじみ不足及び溶け込み不良が発生した。
Comparative Example No. 15 is CaCO3 and Si
Low O2, high Ti and B, and CaCO3/
Because the ratio of CaF2 was small, the arc became too weak, the crater did not spread, and the slag easily got in the way, resulting in insufficient compatibility with the base metal and poor penetration.

【0050】比較例No.16は、CaF2とSiO2
が多く、しかもCaCO3/CaF2の比が小さいため
、スラグが邪魔して母材とのなじみが悪い。
Comparative Example No. 16 is CaF2 and SiO2
Since the CaCO3/CaF2 ratio is large and the ratio of CaCO3/CaF2 is small, the slag interferes and the compatibility with the base material is poor.

【0051】比較例No.17は、CaCO3が多く、
3時(9時)の位置でスラグがやや邪魔し易くビードの
なじみが悪い。
Comparative Example No. 17 has a lot of CaCO3,
At the 3 o'clock (9 o'clock) position, the slag tends to get in the way and the bead does not fit well.

【0052】比較例No.18は、CaF2が少ないの
で、CaCO3/CaF2の比及びFe/CaF2の比
が大きくなりすぎスラグの安定性及びビードのなじみが
悪い。しかもSrCO2が多いのでスラグの剥離性も悪
くなっている。
Comparative Example No. No. 18 has a small amount of CaF2, so the ratio of CaCO3/CaF2 and the ratio of Fe/CaF2 become too large, resulting in poor slag stability and bead conformability. Moreover, since there is a large amount of SrCO2, the slag removability is also poor.

【0053】比較例No.19は、Mnが多いため、脱
酸過剰となり、ビード表面にピットが発生した。
Comparative Example No. Sample No. 19 contained a large amount of Mn, resulting in excessive deoxidation, and pits were generated on the bead surface.

【0054】比較例No.20は、SrCO3及びTi
O2が低いのでビードのなじみが悪い。しかもFeが高
いのでスラグの被包性が悪い。またSiが低いのでブロ
ーホールが発生した。
Comparative Example No. 20 is SrCO3 and Ti
Beads do not conform well due to low O2. Moreover, since the Fe content is high, the slag encapsulation property is poor. In addition, blowholes occurred because the Si content was low.

【0055】比較例No.21は、Fe/CaF2の比
が低すぎるので、6時の位置でビードが垂れ易くなり、
なじみが悪くなる。またSiが高いので脱酸過剰となり
、ビード表面にピットが発生した。
Comparative Example No. 21 has a too low Fe/CaF2 ratio, so the bead tends to droop at the 6 o'clock position.
Familiarity deteriorates. Further, since the Si content was high, deoxidation was excessive, and pits were generated on the bead surface.

【0056】比較例No.22は、TiO2が多いので
スラグが邪魔し易くなり、ビードと母材のなじみが悪い
。またMnが少ないのでブローホールが発生した。
Comparative Example No. No. 22 has a large amount of TiO2, so the slag easily gets in the way, and the bead and base metal do not fit well. In addition, blowholes occurred due to the low Mn content.

【0057】比較例No.23は、Niが多いのでアー
クが弱くなり溶滴移行性が悪いため、溶け込み不良が発
生した。
Comparative Example No. Sample No. 23 had a large amount of Ni, which weakened the arc and caused poor droplet transfer, resulting in poor penetration.

【0058】[0058]

【発明の効果】以上詳述したように、本発明によれば、
特にパイプの円周突合せ継手の下進溶接において全姿勢
で溶接可能となり、特に4.5時〜6時(7.5時〜6
時)の位置でビードと母材のなじみが優れているので、
手直し作業が不要であり、高能率化も可能である。更に
は、これらの優れた効果のほか、アークの集中性及び母
材とのなじみを更に向上させることもできるので、高度
な溶接技術を必要とせず溶接作業が非常にやり易い効果
も得られる。一方、低温靭性の更なる要求に対しても、
フェライト組織の強靱化を図ることにより低温靭性を改
良することもできるという効果も得られる。
[Effects of the Invention] As detailed above, according to the present invention,
Particularly in downward welding of circumferential butt joints of pipes, it is possible to weld in all positions, especially from 4.5 o'clock to 6 o'clock (7.5 o'clock to 6 o'clock).
Since the bead and base metal are well matched at the position (time),
No rework is required and high efficiency is possible. Furthermore, in addition to these excellent effects, the concentration of the arc and its compatibility with the base metal can be further improved, so that the welding work can be performed very easily without requiring sophisticated welding techniques. On the other hand, in response to further demands for low-temperature toughness,
By strengthening the ferrite structure, it is also possible to improve low-temperature toughness.

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

【図1】パイプの円周突合せ継手の下進溶接における溶
接位置を時計式に表わした説明図である。
FIG. 1 is an explanatory diagram showing welding positions in downward welding of a circumferential butt joint of a pipe in a clockwise manner.

【図2】衝撃試験片の採取位置を示す図である。FIG. 2 is a diagram showing the sampling positions of impact test pieces.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】  重量%で(以下、同じ)、CaCO3
:35〜55%、SrCO3:1〜4%、CaF2:1
.5〜4%、TiO2:1〜5%、SiO2:5〜12
%、Si:3〜9%、Mn:1〜6%及びFe:15〜
40%を含有し、かつ、CaCO3/CaF2:9〜2
5、Fe/CaF2:5〜22の関係を満たす被覆剤を
鋼心線外周に塗布してなることを特徴とする低水素系被
覆アーク溶接棒。
[Claim 1] In weight% (hereinafter the same), CaCO3
:35-55%, SrCO3:1-4%, CaF2:1
.. 5-4%, TiO2: 1-5%, SiO2: 5-12
%, Si: 3-9%, Mn: 1-6% and Fe: 15-
40%, and CaCO3/CaF2:9-2
5. A low hydrogen-based coated arc welding rod, characterized in that a coating agent satisfying the relationship of Fe/CaF2: 5 to 22 is applied to the outer periphery of the steel core wire.
【請求項2】  CaCO3:35〜55%、SrCO
3:1〜4%、CaF2:1.5〜4%、TiO2:1
〜5%、SiO2:5〜12%、Si:3〜9%、Mn
:1〜6%及びFe:15〜40%を含有し、更にTi
:0.5〜3%及びB:0.05〜0.2%を含有し、
かつ、CaCO3/CaF2:9〜25、Fe/CaF
2:5〜22の関係を満たす被覆剤を鋼心線外周に塗布
してなることを特徴とする低水素系被覆アーク溶接棒。
[Claim 2] CaCO3: 35-55%, SrCO
3:1-4%, CaF2:1.5-4%, TiO2:1
~5%, SiO2: 5-12%, Si: 3-9%, Mn
:1 to 6% and Fe:15 to 40%, and further contains Ti.
:0.5-3% and B:0.05-0.2%,
and CaCO3/CaF2:9-25, Fe/CaF
A low hydrogen-based coated arc welding rod characterized in that a coating agent satisfying the relationship of 2:5 to 22 is applied to the outer periphery of a steel core wire.
【請求項3】  被覆剤が更にNi:0.5〜4.5%
を含有していることを特徴とする請求項2に記載の低水
素系被覆アーク溶接棒。
Claim 3: The coating further contains Ni: 0.5 to 4.5%.
The low hydrogen-based coated arc welding rod according to claim 2, characterized in that it contains.
JP20250191A 1990-07-24 1991-07-17 Low hydrogen type coated electrode Pending JPH04367393A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20250191A JPH04367393A (en) 1990-07-24 1991-07-17 Low hydrogen type coated electrode

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
JP19553190 1990-07-24
JP2-195531 1990-07-24
JP20250191A JPH04367393A (en) 1990-07-24 1991-07-17 Low hydrogen type coated electrode

Publications (1)

Publication Number Publication Date
JPH04367393A true JPH04367393A (en) 1992-12-18

Family

ID=26509184

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20250191A Pending JPH04367393A (en) 1990-07-24 1991-07-17 Low hydrogen type coated electrode

Country Status (1)

Country Link
JP (1) JPH04367393A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0796394A (en) * 1993-09-29 1995-04-11 Kobe Steel Ltd Low hydrogen type coated electrode
JP2019171399A (en) * 2018-03-27 2019-10-10 日鉄溶接工業株式会社 Low-hydrogen type coated electrode

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH0796394A (en) * 1993-09-29 1995-04-11 Kobe Steel Ltd Low hydrogen type coated electrode
JP2019171399A (en) * 2018-03-27 2019-10-10 日鉄溶接工業株式会社 Low-hydrogen type coated electrode

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