JPH0796394A - Low hydrogen type coated electrode - Google Patents

Low hydrogen type coated electrode

Info

Publication number
JPH0796394A
JPH0796394A JP26562893A JP26562893A JPH0796394A JP H0796394 A JPH0796394 A JP H0796394A JP 26562893 A JP26562893 A JP 26562893A JP 26562893 A JP26562893 A JP 26562893A JP H0796394 A JPH0796394 A JP H0796394A
Authority
JP
Japan
Prior art keywords
welding
core wire
coating material
rate
welding rod
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
JP26562893A
Other languages
Japanese (ja)
Other versions
JP2711060B2 (en
Inventor
Tomoyuki Abe
阿部知之
Noboru Kasai
登 笠井
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 JP5265628A priority Critical patent/JP2711060B2/en
Publication of JPH0796394A publication Critical patent/JPH0796394A/en
Application granted granted Critical
Publication of JP2711060B2 publication Critical patent/JP2711060B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Abstract

PURPOSE:To provide a low hydrogen type coated electrode preventing sagging, etc., of slag even with single layer single pass welding by a weaving procedure and executing welding with a small number of passes. CONSTITUTION:This low hydrogen type coated electrode is formed by coating the outer periphery of a steel core wire with a coating material contg. 1 to 6% Ti oxide contg. >=40% superfine Ti oxides having a grain size of <=0.3mum in a coating rate range of 20 to 30% and regulating the carbon content by the following equation over the entire part of the welding electrode to 0.08 to 0.25%. The carbon content = (the carbon content in the core wire)+{(the carbon content in the coating material)X(coating rate/core wire rate)}, where the coating rate = (the weight of the coating material/the weight of the entire part of the welding electrode)X100%, the core wire rate = (the weight of the core wire/the weight over the entire part of the welding electrode)X100%. As a result, this welding electrode is suitable for down hand welding of particularly the circumferential butt joints of pipes.

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, particularly, to an excellent effect when applied to downward welding of a circumferential butt joint of a pipe.

【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、従来は、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。
2. Description of the Related Art Conventionally, circumferential butt welding at a pipeline site has been performed in Japan by upward welding using a low-hydrogen coated arc welding rod or an illuminate-based coated arc welding rod. In foreign countries, downward welding using a high-cellulosic coated arc welding rod is performed. But,
Since hydrogen cracking is a major problem in welding high-strength steel pipes, especially in field welding in cold regions, it is desirable to use a low-hydrogen coated arc welding rod. It was very difficult to weld in.

【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開平4−367393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。
In order to solve this problem, the applicant of the present invention has previously proposed JP-A-4-376393. However, the low-hydrogen coated arc welding rod of the above-mentioned proposal has significantly superior performance as compared with those before it, but recently, higher efficiency, severer performance has been required, It was not always satisfactory, and improvements were required.

【0004】すなわち、高能率化を図るために、パス数
をできる限り少なくした1層1パス溶接が望まれてい
る。つまり、1層2パス溶接の場合は、第1ビードを溶
接した後、第2ビードを溶接する前に開先内の第1ビー
ド止端部をグラインダー等で研削して、開先を広げて溶
込み不足などを防止していた。しかし、その作業に時間
がかかるため、1層1パスで溶接すれば、上記の工程が
不要なことから、1層1パスが可能な低水素系被覆アー
ク溶接棒が望まれていた。
That is, in order to achieve high efficiency, one-layer one-pass welding in which the number of passes is reduced as much as possible is desired. That is, in the case of 1-layer 2-pass welding, after welding the first bead, before welding the second bead, grind the first bead toe portion in the groove with a grinder or the like to widen the groove. Prevents insufficient penetration. However, since the work takes time, the above steps are not required if the welding is performed in one layer and one pass. Therefore, a low hydrogen system covered arc welding rod capable of performing one layer and one pass has been desired.

【0005】しかしながら、従来の低水素系被覆アーク
溶接棒では、1層1パス溶接をするためにウィービング
施工を行うと、スラグが垂れやすく、溶接金属の垂れが
発生しやすい欠点があった。
However, in the conventional low hydrogen type covered arc welding rod, when weaving is carried out for one-layer one-pass welding, there is a drawback that the slag is liable to droop and the dripping of the weld metal is likely to occur.

【0006】また、従来の低水素系被覆アーク溶接棒で
は、裏波溶接を高能率に施工しようとして高電流、高溶
接速度の条件で行うと、スラグが垂れやすく、溶接金属
が凹形の裏波ビードになる欠点があった。
Further, in the conventional low hydrogen system coated arc welding rod, if the backside welding is carried out under the conditions of high current and high welding speed in order to carry out high efficiency welding, the slag tends to drip and the weld metal has a concave backing. It had the drawback of becoming a wave bead.

【0007】本発明は、上記従来技術の欠点を解消し
て、ウィービング施工による1層1パス溶接でもスラグ
の垂れ等を防止し得る結果、少ないパス数による溶接施
工が可能となる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。
The present invention solves the above-mentioned drawbacks of the prior art and can prevent the slag from sagging even in the one-layer one-pass welding by the weaving process. As a result, the welding process can be performed with a small number of passes. It is intended to provide an arc welding rod.

【0008】[0008]

【課題を解決するための手段】以上の状況において、本
発明者らは、まず、スラグの垂れを防止する方法を検討
した。従来の溶接棒はアークの広がりが少なく、また溶
滴移行も安定性に欠け、その結果、ウィービングを行っ
た時、クレータの広がりが不充分でスラグが垂れやすい
ことが判明した。したがって、クレータの広がりを充分
確保し、かつアークをスプレー化し、溶滴移行を安定に
させる手段について種々検討した。その結果、超微粒の
Ti酸化物を添加することにより、保護筒が安定し、つ
まり保護筒が均一に溶融して、アークの方向性が安定
し、クレータの広がりを制御しやすいことが判明した。
Under the above circumstances, the present inventors first examined a method for preventing slag sag. It was found that the conventional welding rod has a small arc spread and lacks stability in droplet transfer, and as a result, when weaving is performed, the spread of the crater is insufficient and the slag tends to droop. Therefore, various investigations were made on means for securing the spread of the crater, making the arc into a spray, and stabilizing the droplet transfer. As a result, it was found that by adding ultrafine Ti oxide, the protective cylinder was stabilized, that is, the protective cylinder was melted uniformly, the directionality of the arc was stabilized, and the spread of the crater was easily controlled. .

【0009】従来の溶接棒ではストレートに近い施工で
且つコンタクト溶接であるため、保護筒の安定性はそれ
ほど問題にはならなかったが、ウィービング施工におい
ては、若干溶接棒を母材から離して施工するため、より
保護筒の均一な溶融性が必要となり、これが、従来の溶
接棒ではウィービング施工に適さなかった理由と考えら
れた。
With conventional welding rods, since the work is almost straight and contact welding is performed, the stability of the protective cylinder does not pose a serious problem, but in the weaving work, the welding rod is slightly separated from the base metal. Therefore, it is necessary that the protective cylinder has more uniform meltability, which is considered to be the reason why the conventional welding rod is not suitable for weaving.

【0010】しかしながら、超微粒のTi酸化物は、上
記の効果が得られるものの、一方では、スパッタ量は充
分少なくならず、後工程でのスパッタ除去や溶接中の安
全面でより一層の改善が必要であることが判明した。
[0010] However, although the ultrafine-grained Ti oxide can obtain the above-mentioned effects, on the other hand, the amount of spatter is not sufficiently reduced, and further improvement can be made in terms of spatter removal in the subsequent process and safety during welding. It turned out to be necessary.

【0011】そこで、本発明者らは種々の成分を検討し
た結果、従来の低水素系被覆剤では耐割れ性の点で低い
のが望ましいとされていた炭素量を逆に増加させること
で、アークを安定化させ、かつスパッタの発生量も減少
できることを見い出し、ここに本発明を完成したもので
ある。
Therefore, as a result of studying various components, the present inventors conversely increase the amount of carbon, which is considered to be low in the crack resistance in the conventional low hydrogen type coating agent. It was found that the arc can be stabilized and the amount of spatter generated can be reduced, and the present invention has been completed here.

【0012】すなわち、本発明は、被覆剤全重量%で、
金属炭酸塩:30〜50%、金属フッ化物:1.5〜4
%、SiO2:5〜12%、Ti酸化物:1〜6%(但し、
粒径0.3μm以下である超微粒Ti酸化物を40%以上
含有すること。)、Si:3〜9%、Mn:1〜6%、F
e:25〜50%、を含有した被覆剤を、鋼心線外周に
被覆率20〜35%の範囲で塗布してなり、且つ溶接棒
全体の下記(1)式による炭素量を0.08〜0.25%に
規制してなることを特徴とする低水素系被覆アーク溶接
棒を要旨としている。 記 炭素量=(心線中の炭素量)+{(被覆剤中の炭素量)×(被覆率/心線率)}…(1) ここで、 被覆率=(被覆剤の重量/溶接棒全体の重量)×100% 心線率=(心線の重量/溶接棒全体の重量)×100%
That is, the present invention is based on the total weight% of the coating agent,
Metal carbonate: 30-50%, metal fluoride: 1.5-4
%, SiO 2 : 5 to 12%, Ti oxide: 1 to 6% (however,
Contain 40% or more of ultrafine Ti oxide having a particle size of 0.3 μm or less. ), Si: 3 to 9%, Mn: 1 to 6%, F
The coating material containing e: 25 to 50% is applied to the outer circumference of the steel core wire in a coverage of 20 to 35%, and the carbon content of the entire welding rod according to the following formula (1) is 0.08. The gist is a low-hydrogen coated arc welding rod characterized by being regulated to 0.25%. Notation Carbon amount = (carbon amount in core wire) + {(carbon amount in coating material) x (coverage rate / core rate)} (1) where, coverage rate = (weight of coating material / welding rod) Total weight) x 100% Core wire rate = (core wire weight / total weight of welding rod) x 100%

【0013】また、他の本発明は、被覆剤が更に、N
i:0.5〜4.5%、Mo:0.1〜4.5%、Ti:0.1
〜3%のうちの1種又は2種以上、及び/又は、B:
0.05〜0.2%を含有していることを特徴としてい
る。
According to another aspect of the present invention, the coating material further comprises N
i: 0.5-4.5%, Mo: 0.1-4.5%, Ti: 0.1
~ 1% or more of 3%, and / or B:
It is characterized by containing 0.05 to 0.2%.

【0014】[0014]

【作用】まず、本発明における各成分並びに被覆率の限
定理由は以下のとおりである。
The reasons for limiting the components and the coverage in the present invention are as follows.

【0015】金属炭酸塩:30〜50% 金属炭酸塩はガス発生剤として添加するが、30%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す
る。一方、50%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、金属炭
酸塩量は30〜50%の範囲とする。なお、金属炭酸塩
は例えばCaCO3、BaCO3、MgCO3などが使われ
る。
Metal carbonate: 30 to 50% Metal carbonate is added as a gas generating agent, but if it is less than 30%, the amount of gas generated is small and the shield becomes insufficient and the viscosity of the slag becomes small and pits are formed on the bead surface. To do. On the other hand, if it exceeds 50%, the viscosity of the slag remarkably increases, the familiarity of the bead deteriorates, and the amount of gas generation increases and the generation of spatter increases. Therefore, the amount of metal carbonate is set in the range of 30 to 50%. As the metal carbonate, for example, CaCO 3 , BaCO 3 , MgCO 3 or the like is used.

【0016】金属フッ化物:1.5〜4% 金属フッ化物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2〜4時の位置で良好なビードが形成さ
せるが、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、4.5〜6時及び7.5〜
6時の位置(図1参照)においてビードと母材のなじみが
悪くなる。したがって、金属フッ化物量は1.5〜4%
の範囲とする。なお、金属フッ化物としては例えばCa
2等々が使われる。
Metal Fluoride: 1.5 to 4% Metal Fluoride acts to adjust the viscosity and fluidity of the slag. However, if it is less than 1.5%, there is no effect, and if it is more than this, good beads are formed at the position of 2 to 4 o'clock, but if it exceeds 4%, the viscosity of the slag becomes relatively small, and the fluidity of the slag becomes relatively small. Increase, 4.5 to 6 o'clock and 7.5 to
At the 6 o'clock position (see FIG. 1), the bead and base metal become less compatible. Therefore, the amount of metal fluoride is 1.5-4%
The range is. As the metal fluoride, for example, Ca
F 2 etc. are used.

【0017】SiO2:5〜12% SiO2はアークを強くして溶込みを確保する作用があ
る。しかし、5%未満ではアークが弱く、クレータの広
がりが小さい。またビードのなじみも劣化する。一方、
12%を超えると2〜4時の位置において、スラグが邪
魔し巻き込み易くなり、良好なビードが得られなくな
る。したがって、SiO2量は5〜12%の範囲とする。
SiO 2 : 5 to 12% SiO 2 has a function of strengthening the arc to secure penetration. However, if it is less than 5%, the arc is weak and the spread of the crater is small. Also, the familiarity of the beads is deteriorated. on the other hand,
When it exceeds 12%, the slag interferes with the position at 2 to 4 o'clock, and it is easy to be involved, so that a good bead cannot be obtained. Therefore, the amount of SiO 2 is set in the range of 5 to 12%.

【0018】Ti酸化物:1〜6%(但し、粒径0.3μm
以下の超微粒Ti酸化物を40%以上含むこと) Ti酸化物は保護筒の溶融を均一化することにより、ア
ークの方向性が一定になり、ウィービング施工において
も溶接金属の垂れを防止する効果がある。そのために
は、粒径0.3μm以下の超微粒Ti酸化物を40%以上
含んだTi酸化物を1〜6%含有させることが必要であ
る。1%未満ではその効果が得られず、更にビードのな
じみも劣化する。また6%を超えるとスラグの流動性が
増し、2〜4時の位置でスラグ邪魔が生じやすい。
Ti oxide: 1 to 6% (however, the particle size is 0.3 μm
40% or more of the following ultrafine Ti oxides should be included.) The Ti oxides have the effect of preventing the sagging of the weld metal even during weaving work by making the arc of the arc uniform by homogenizing the melting of the protective cylinder. There is. For that purpose, it is necessary to contain 1 to 6% of Ti oxide containing 40% or more of ultrafine Ti oxide having a particle size of 0.3 μm or less. If it is less than 1%, the effect cannot be obtained, and the familiarity of the bead is deteriorated. On the other hand, if it exceeds 6%, the fluidity of the slag increases, and the slag hindrance is likely to occur at the 2-4 o'clock position.

【0019】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、Mnは金属Mn或いはFe−Mn、Si
−Mn等の形で添加できる。
Si: 3 to 9%, Mn: 1 to 6% Si and Mn are added as deoxidizing agents, but if each is less than the lower limit value, there is no effect, and if it exceeds the upper limit value, deoxidation becomes excessive. Pits will be generated on the bead surface.
Si is a single substance or Fe-Si, Si-Mn, Ca-Si.
Can be added in the form of Mn, Mn is metallic Mn or Fe-Mn, Si
-Mn or the like can be added.

【0020】Fe:25〜50% Feは溶着効率を向上させるために添加するが、25%
未満ではその効果が少なく、また50%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25〜50%の範囲と
する。なお、Feは鉄粉として、又はFe−Mn、Fe−S
i等のFe分として添加できる。
Fe: 25 to 50% Fe is added to improve the welding efficiency, but 25%
If it is less than 50%, the effect is small, and if it exceeds 50%, the amount of the slag forming agent is relatively small, and the slag encapsulating property is deteriorated. Therefore, the Fe amount is in the range of 25 to 50%. Fe is iron powder, or Fe-Mn, Fe-S
It can be added as Fe component such as i.

【0021】被覆率:20〜35% 被覆率が20%未満ではスラグ形成剤が少なくなり、シ
ールド不足によるピットが発生する。また35%を超え
るとスラグ形成剤が多くなりすぎ、スラグの邪魔が発生
し、良好なビードが得られない。したがって、被覆率は
20〜35%の範囲とする。
Coverage: 20-35% If the coverage is less than 20%, the amount of slag-forming agent decreases, and pits are generated due to insufficient shield. On the other hand, if it exceeds 35%, the amount of the slag-forming agent becomes too much, the slag is disturbed, and good beads cannot be obtained. Therefore, the coverage is set to the range of 20 to 35%.

【0022】炭素量(式(1)の値):0.08〜0.25% 下記の(1)式で定義される炭素量が0.08%未満では
溶滴が大粒になり、スパッタが増し、また、0.25%
を超えるとアークが強くなりすぎて、クレータを掘り下
げ溶接金属が垂れやすくなったり、またスパッタ量もや
や増すことが判明した。したがって、本発明では下記の
(1)式で定義される炭素量を0.08〜0.25%の範囲
に規制する。より好ましくは0.12〜0.20%であ
る。
Carbon amount (value of formula (1)): 0.08 to 0.25% If the carbon amount defined by the following formula (1) is less than 0.08%, the droplets become large and spatter occurs. Increased, also 0.25%
It has been found that the arc becomes too strong when the temperature exceeds the limit, the crater is dug down, the weld metal is easily dropped, and the amount of spatter is slightly increased. Therefore, in the present invention,
The amount of carbon defined by the formula (1) is regulated within the range of 0.08 to 0.25%. It is more preferably 0.12 to 0.20%.

【0023】 炭素量=(心線中の炭素量)+{(被覆剤中の炭素量)×(被覆率/心線率)}…(1) ここで、 被覆率=(被覆剤の重量/溶接棒全体の重量)×100% 心線率=(心線の重量/溶接棒全体の重量)×100%Carbon amount = (carbon amount in core wire) + {(carbon amount in coating material) × (coverage rate / core wire rate)} (1) where, coating rate = (weight of coating material / Welding rod total weight) x 100% Core wire ratio = (core wire weight / welding rod total weight) x 100%

【0024】なお、上記成分のほか、必要に応じて、以
下の成分の1種又は2種以上を適量にて被覆剤中に添加
することができる。
In addition to the above components, if necessary, one or more of the following components may be added to the coating agent in an appropriate amount.

【0025】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 for strengthening the toughness of the ferrite structure, but if it is less than 0.5%, the effect is not obtained, while on the other hand, it is 4.5.
If it exceeds%, the arc becomes weak and the droplet transferability deteriorates, resulting in poor penetration. Therefore, the amount of Ni is 0.5-
The range is 4.5%.

【0026】Mo:0.1〜4.5% Moは強度の調整のために有効であるが、0.1%未満で
はその効果が得られず、一方、4.5%を超えると衝撃
値が劣化する。したがって、Mo量は0.1〜4.5%と
する。
Mo: 0.1-4.5% Mo is effective for adjusting the strength, but if it is less than 0.1%, the effect cannot be obtained. On the other hand, if it exceeds 4.5%, an impact value is obtained. Deteriorates. Therefore, the Mo amount is set to 0.1 to 4.5%.

【0027】Ti:0.1〜3% 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点
である。しかし、0.1%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り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込み
不良が発生する。したがって、Ti量は0.1〜3%の範
囲とする。なお、Tiは例えばFe−Ti等の形態で添加
する。
Ti: 0.1 to 3% The effect of Ti on the welding workability is that the concentration of the arc can be improved and the arc can be softened. However, if it is less than 0.1%, the concentration of the arc is poor, which causes a defective fusion and requires skill in operating the rod. On the other hand, if it exceeds 3%, the arc becomes too weak, resulting in poor penetration. Therefore, the Ti amount is set in the range of 0.1 to 3%. Incidentally, Ti is added in the form of, for example, Fe-Ti.

【0028】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%未満では母材とのなじみが劣るので、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。なお、BはB合金若
しくはB酸化物の形態で添加することができる。
B: 0.05 to 0.2% B is effective for improving the compatibility with the base material,
If it is less than 0.05%, the familiarity with the base material is poor, so skill is required in operating the rod. If it exceeds 0.2%, the arc becomes too weak, resulting in defective penetration. Therefore, the amount of B is set in the range of 0.05 to 0.2%. B can be added in the form of B alloy or B oxide.

【0029】なお、溶着金属の機械的性質を調整するた
めにCr、Cu、Nb等の合金成分の1種類以上を被覆剤
又は心線中に添加してもよい。鋼心線の他の成分組成は
特に限定されない。
In order to adjust the mechanical properties of the deposited metal, one or more alloy components such as Cr, Cu and Nb may be added to the coating material or the core wire. The other component composition of the steel core wire is not particularly limited.

【0030】また、本発明では通常粘性剤として水ガラ
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。なお、直流電源を使用する場合に
は水ガラスとしてK2Oを含まないものの方が保護筒が
より安定して好ましい。
In the present invention, water glass is usually used as a viscous agent, but since water glass contains a small amount of components such as Na 2 O and K 2 O, it is used as a slag forming agent and an arc stabilizer. Also works. When a DC power source is used, it is preferable that the water glass does not contain K 2 O because the protective cylinder is more stable.

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

【実施例】【Example】

【0032】鋼心線に、表1及び表3に示す成分組成の
被覆剤を被覆率20〜35%の範囲で塗布して、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1層1パス溶接にて溶接条件:電流80〜2
20A、電圧18〜28V、溶接速度10〜25cm/mi
nで下進で溶接し、各溶接位置における作業性を調査し
た。その結果を表2に併記する。
A coating rod having the composition shown in Tables 1 and 3 was applied to the steel core wire in a coating ratio range of 20 to 35% to prepare a trial welding rod. Using these test welding rods, a horizontal fixed pipe (10.3 mmt x 1016 mmφ) butt joint (60 °
V groove) with 1 layer 1 pass welding Welding condition: current 80-2
20A, voltage 18-28V, welding speed 10-25cm / mi
Welding was performed downward at n and the workability at each welding position was investigated. The results are also shown in Table 2.

【0033】表中、No.1〜No.10はいずれも本発明
例であり、良好な結果を示した。溶接金属の垂れ、スラ
グの垂れもなく、スパッタ発性量も少ない。
In the table, No. 1 to No. 10 are all examples of the present invention and showed good results. No welding metal slag, no slag dripping, and little spatter generation.

【0034】これに対し、比較例のNo.11は、金属炭
酸塩が多すぎ、スパッタ発生量が増し、かつスラグの安
定性に欠けた。またTi酸化物中の超微粒Ti酸化物量が
40%未満であり、溶接金属の安定性(垂れ)に欠けた。
On the other hand, in Comparative Example No. 11, the amount of metal carbonate was too much, the amount of spatter was increased, and the stability of the slag was lacking. Further, the amount of ultrafine Ti oxide in the Ti oxide was less than 40%, and the weld metal lacked stability (sagging).

【0035】比較例No.12は、Ti酸化物が多すぎス
ラグの邪魔が生じている。また(1)式の炭素量も低いた
めスパッタが多発した。また金属フッ化物が多く、スラ
グの流動性が増し、母材とのなじみが劣化した。
In Comparative Example No. 12, the Ti oxide was too much and the slag was disturbed. Further, since the carbon content in the formula (1) is low, spatter frequently occurred. In addition, the amount of metal fluoride was large, the fluidity of the slag increased, and the compatibility with the base material deteriorated.

【0036】比較例No.13は、SiO2量が多く、スラ
グの邪魔が生じている。また(1)式の炭素量が高すぎて
溶接金属の安定性が劣化した。
In Comparative Example No. 13, the amount of SiO 2 was large and the slag was disturbed. Further, the carbon content in the formula (1) was too high, and the stability of the weld metal deteriorated.

【0037】[0037]

【表1】 [Table 1]

【0038】[0038]

【表2】 [Table 2]

【0039】[0039]

【表3】 [Table 3]

【0040】[0040]

【発明の効果】以上詳述したように、本発明の低水素系
被覆アーク溶接棒によれば、ウィービング施工による1
層1パス溶接でも、スラグの垂れ等を防止することがで
き、少ないパス数による施工が達成できる。また裏波施
工も可能である。
As described above in detail, according to the low hydrogen type covered arc welding rod of the present invention, the welding electrode 1
Even in the layer 1 pass welding, it is possible to prevent the slag from dripping, and it is possible to achieve construction with a small number of passes. It is also possible to use Uranami.

【図面の簡単な説明】[Brief description 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 in which a welding position in a downward welding of a circumferential butt joint of a pipe is represented by a clock type.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 被覆剤全重量%で(以下、同じ)、 金属炭酸塩:30〜50%、 金属フッ化物:1.5〜4%、 SiO2:5〜12%、 Ti酸化物:1〜6%(但し、粒径0.3μm以下である超
微粒Ti酸化物を40%以上含有すること。)、 Si:3〜9%、 Mn:1〜6%、 Fe:25〜50%、を含有した被覆剤を、鋼心線外周
に被覆率20〜35%の範囲で塗布してなり、且つ溶接
棒全体の下記(1)式による炭素量を0.08〜0.25%
に規制してなることを特徴とする低水素系被覆アーク溶
接棒。 記 炭素量=(心線中の炭素量)+{(被覆剤中の炭素量)×(被覆率/心線率)}…(1) ここで、 被覆率=(被覆剤の重量/溶接棒全体の重量)×100% 心線率=(心線の重量/溶接棒全体の重量)×100%
1. A coating material based on the total weight% (hereinafter the same), metal carbonate: 30 to 50%, metal fluoride: 1.5 to 4%, SiO 2 : 5 to 12%, Ti oxide: 1 ~ 6% (however, containing 40% or more of ultrafine Ti oxide having a particle size of 0.3 µm or less), Si: 3 to 9%, Mn: 1 to 6%, Fe: 25 to 50%, Is applied to the outer circumference of the steel core wire in a coverage of 20 to 35%, and the carbon content of the entire welding rod according to the following formula (1) is 0.08 to 0.25%.
A low-hydrogen coated arc welding rod characterized by being regulated according to. Notation Carbon amount = (carbon amount in core wire) + {(carbon amount in coating material) x (coverage rate / core rate)} (1) where, coverage rate = (weight of coating material / welding rod) Total weight) x 100% Core wire rate = (core wire weight / total weight of welding rod) x 100%
【請求項2】 被覆剤が更に、Ni:0.5〜4.5%、
Mo:0.1〜4.5%、Ti:0.1〜3%のうちの1種
又は2種以上を含有していることを特徴とする請求項1
に記載の低水素系被覆アーク溶接棒。
2. The coating material further comprises Ni: 0.5-4.5%,
2. One or more of Mo: 0.1 to 4.5% and Ti: 0.1 to 3% are contained.
The low-hydrogen coated arc welding rod according to 1.
【請求項3】 被覆剤が更に、B:0.05〜0.2%を
含有していることを特徴とする請求項1又は2に記載の
低水素系被覆アーク溶接棒。
3. The low-hydrogen coated arc welding rod according to claim 1, wherein the coating material further contains B: 0.05 to 0.2%.
JP5265628A 1993-09-29 1993-09-29 Low hydrogen coated arc welding rod Expired - Lifetime JP2711060B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5265628A JP2711060B2 (en) 1993-09-29 1993-09-29 Low hydrogen coated arc welding rod

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5265628A JP2711060B2 (en) 1993-09-29 1993-09-29 Low hydrogen coated arc welding rod

Publications (2)

Publication Number Publication Date
JPH0796394A true JPH0796394A (en) 1995-04-11
JP2711060B2 JP2711060B2 (en) 1998-02-10

Family

ID=17419780

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5265628A Expired - Lifetime JP2711060B2 (en) 1993-09-29 1993-09-29 Low hydrogen coated arc welding rod

Country Status (1)

Country Link
JP (1) JP2711060B2 (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004306094A (en) * 2003-04-08 2004-11-04 Nippon Steel & Sumikin Welding Co Ltd Low hydrogen-based tack welding rod
JP2009291802A (en) * 2008-06-03 2009-12-17 Nippon Steel Corp Low hydrogen covered electrode for welder using dc power source
JP2014151338A (en) * 2013-02-07 2014-08-25 Kobe Steel Ltd Low hydrogen type covered electrode

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61229494A (en) * 1985-04-03 1986-10-13 Nippon Steel Corp Low hydrogen type coated arc electrode
JPS62161496A (en) * 1986-01-09 1987-07-17 Kawasaki Steel Corp Covered electrode for cr-mo high temperature steel
JPH04367393A (en) * 1990-07-24 1992-12-18 Kobe Steel Ltd Low hydrogen type coated electrode

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS61229494A (en) * 1985-04-03 1986-10-13 Nippon Steel Corp Low hydrogen type coated arc electrode
JPS62161496A (en) * 1986-01-09 1987-07-17 Kawasaki Steel Corp Covered electrode for cr-mo high temperature steel
JPH04367393A (en) * 1990-07-24 1992-12-18 Kobe Steel Ltd Low hydrogen type coated electrode

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2004306094A (en) * 2003-04-08 2004-11-04 Nippon Steel & Sumikin Welding Co Ltd Low hydrogen-based tack welding rod
JP2009291802A (en) * 2008-06-03 2009-12-17 Nippon Steel Corp Low hydrogen covered electrode for welder using dc power source
JP2014151338A (en) * 2013-02-07 2014-08-25 Kobe Steel Ltd Low hydrogen type covered electrode

Also Published As

Publication number Publication date
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