Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS5914315B2 - Low hydrogen coated arc welding rod - Google Patents
[go: Go Back, main page]

JPS5914315B2 - Low hydrogen coated arc welding rod - Google Patents

Low hydrogen coated arc welding rod

Info

Publication number
JPS5914315B2
JPS5914315B2 JP5001980A JP5001980A JPS5914315B2 JP S5914315 B2 JPS5914315 B2 JP S5914315B2 JP 5001980 A JP5001980 A JP 5001980A JP 5001980 A JP5001980 A JP 5001980A JP S5914315 B2 JPS5914315 B2 JP S5914315B2
Authority
JP
Japan
Prior art keywords
slag
welding
amount
bead
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.)
Expired
Application number
JP5001980A
Other languages
Japanese (ja)
Other versions
JPS56144895A (en
Inventor
芳也 酒井
真澄 遠藤
茂雄 長岡
登 笠井
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 JP5001980A priority Critical patent/JPS5914315B2/en
Publication of JPS56144895A publication Critical patent/JPS56144895A/en
Publication of JPS5914315B2 publication Critical patent/JPS5914315B2/en
Expired legal-status Critical Current

Links

Landscapes

  • Nonmetallic Welding Materials (AREA)

Description

【発明の詳細な説明】 本発明は溶接作業性及び継手性能の優れた低水素系被覆
アーク溶接棒に関するものである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a low-hydrogen coated arc welding rod that has excellent welding workability and joint performance.

船体構造用鋼板として50kg/md級の高張力鋼5板
の需要が増大している。この種の鋼板の溶接には、拡散
性水素に起因する遅れ割れを防止する為低水素系溶接棒
が使用されている。しかし低水素系溶接棒を用いると、
継手性能殊に耐ペイント性(ピットの発生防止等)及び
溶接性が悪く手直し10溶接の対象となることが多い。
一方継手性能(耐ペイント性)を改善した低水素系溶接
棒も開発されてはいるが、ビードが凸状化して外観が悪
化するほかビード上端部で応力集中を起こし易くなる等
の欠点がある。15本発明は前述の様な事情に着目して
なされたものであつて、優れた継手性能を維持しつつビ
ードの外観及び上端部の応力集中を改善し得る様な低水
素系被覆アーク溶接棒の提供を目的とする。
There is an increasing demand for 50 kg/md class high tensile strength steel plates as steel plates for ship hull structures. In welding this type of steel plate, a low-hydrogen welding rod is used to prevent delayed cracking caused by diffusible hydrogen. However, when using a low hydrogen welding rod,
Joint performance, especially paint resistance (prevention of pits, etc.) and weldability are poor, and it is often subject to rework 10 welding.
On the other hand, low-hydrogen welding rods with improved joint performance (paint resistance) have been developed, but they have drawbacks such as a convex bead, which worsens the appearance, and stress concentration at the upper end of the bead. . 15 The present invention was made in view of the above-mentioned circumstances, and provides a low-hydrogen coated arc welding rod that can improve the appearance of the bead and the stress concentration at the upper end while maintaining excellent joint performance. The purpose is to provide.

あわせてアーク安定性、耐アンダーカット性、スラブ0
グ剥離性等の優れた低水素系被覆アーク溶接棒を提供
しようとするものである。しかして本発明に係る低水素
系被覆アーク溶接棒とは、MgO:5〜24%、TiO
2:6〜25%、SiO2:3〜20%、金属フッ化物
:3〜2515%、CO2をMgCO3の形で、MgC
03に換算して5〜25%、Fe及び/又はMnの酸化
物:2〜10%、Si、、Mg、、Al及びTiから選
択される1種以上の元素:0.5〜8%、Mn:2〜1
0%を夫々含み、且つ(Fe酸化物及びMn酸90化物
)の含有量をY%、〔(Si、Mg、Al、Ti)+1
15Mn〕の含有量をX%とした場合のXとYの関係が
次式を満足する被覆剤を、(X/2−1)≦Y≦(X/
2+6) ?5 鋼心線に塗布してなるものである。
In addition, arc stability, undercut resistance, and 0 slabs
The present invention aims to provide a low hydrogen-based coated arc welding rod with excellent peelability. However, the low hydrogen-based coated arc welding rod according to the present invention includes MgO: 5 to 24%, TiO
2: 6-25%, SiO2: 3-20%, metal fluoride: 3-2515%, CO2 in the form of MgCO3, MgC
5 to 25% in terms of 03, oxides of Fe and/or Mn: 2 to 10%, one or more elements selected from Si, Mg, Al and Ti: 0.5 to 8%, Mn: 2-1
0%, respectively, and the content of (Fe oxide and Mn acid 90ide) is Y%, [(Si, Mg, Al, Ti) + 1
15Mn] content is X%, the relationship between X and Y satisfies the following formula: (X/2-1)≦Y≦(X/
2+6)? 5 It is made by coating a steel core wire.

即ち本発明では被覆剤の成分組成を特定することによつ
て前述の目的を達成したもので、これを水ガラス系粘結
剤等と共に混練して鋼心線に塗布することにより、高張
力鋼板用として優れた性能を有する低水素系被覆アーク
溶接棒が得られる。
That is, in the present invention, the above-mentioned object has been achieved by specifying the composition of the coating material, and by kneading this with a water glass-based binder and applying it to the steel core wire, high-tensile steel sheets can be formed. A low hydrogen-based coated arc welding rod with excellent performance for practical use is obtained.

以下本発明における数値範囲設定の根拠を述べる。1M
g0:5〜24% MgOはスラグ生成剤及び粘性調整剤として作用し、ス
ラグの被包性を向上させる。
The basis for setting the numerical range in the present invention will be described below. 1M
g0: 5-24% MgO acts as a slag forming agent and a viscosity modifier and improves the encapsulation properties of the slag.

また塩基性酸化物であるから、他の酸性同効物質(Si
O2やTiO2等)の様に溶接金属の機械的性質を劣下
させる恐れがない。
Also, since it is a basic oxide, other acidic equivalent substances (Si
There is no risk of deteriorating the mechanical properties of the weld metal unlike O2, TiO2, etc.).

5%未満でぱ上記の効果が有意に発揮されず、スラグの
粘性不足によつてアンダーカツトが多発し、或はスラグ
の塩基度が低下して溶接金属の機械的性質が劣化する。
If it is less than 5%, the above-mentioned effects will not be exhibited significantly, and undercuts will occur frequently due to insufficient viscosity of the slag, or the basicity of the slag will decrease, resulting in deterioration of the mechanical properties of the weld metal.

一方24%を越えるとスラグの粘性が増大して被包性が
劣化しビードが凸状になる。なおMgO源としては、ク
リンカーや珪酸塩のほかにドロマイトやMgCO3など
がある。2Ti02:6〜25% スラグ生成剤及び粘性調整剤として作用しスラグ被包性
を高める機能があり、6%未満ではスラグ不足によつて
凸ビード化しアンダーカツトが発生し易くなると共にス
ラグ剥離性が劣化する。
On the other hand, if it exceeds 24%, the viscosity of the slag will increase, the encapsulation will deteriorate, and the beads will become convex. Note that MgO sources include dolomite, MgCO3, and the like in addition to clinker and silicates. 2Ti02: 6 to 25% It functions as a slag forming agent and a viscosity modifier to improve slag envelopment.If it is less than 6%, slag becomes insufficient and becomes convex beads, undercuts are likely to occur, and slag removability is reduced. to degrade.

一方25%を越えると、スラグの流動性 二が増大して
スラグが先行し2段ビードが形成され易くなるほか、見
掛けのスラグ量が増大して適正溶接電流値が高まり、棒
焼けによるアンダーカツトやピツトが多発する。3Si
02:3〜20% スラグ生成剤及び粘性調整剤としての作用があり、特に
粘性に大きな影響を与える成分で、3%未満ではスラグ
の流動状態が不安定になつてビード外観が悪化し、一方
20%を越えるとスラグが硬くなつて剥離が著しく困難
になるほ 5か、酸性酸化物である為に溶接金属の靭性
が劣化する。
On the other hand, if it exceeds 25%, the fluidity of the slag increases and the slag tends to take the lead and form a two-stage bead.In addition, the apparent amount of slag increases, the appropriate welding current value increases, and undercuts due to stick burn occur. and pits occur frequently. 3Si
02: 3 to 20% It acts as a slag forming agent and a viscosity modifier, and is a component that has a particularly large effect on viscosity.If it is less than 3%, the fluid state of the slag becomes unstable and the appearance of the bead deteriorates. If it exceeds 20%, the slag becomes so hard that it becomes extremely difficult to peel it off.Also, since it is an acidic oxide, the toughness of the weld metal deteriorates.

4金属フツ化物:3〜15% 具体例としてはCaF2・AlF3・MgF2、NaF
等が挙げられ、これらは単独で或は2種 ク以上の複合
で配合され得る。
4-metal fluoride: 3-15% Specific examples include CaF2, AlF3, MgF2, NaF
These may be used alone or in combination of two or more types.

これらは溶接金属中の拡散性水素量を低減し耐割れ性を
向上させると共に、母材表面に付着した錆、油脂類、ペ
イント等に起因するピツトやブローホールの発生を防止
する機能がある。3%未満では上記の機能が有意に発揮
されず、拡散性水素量の増大によつて耐割れ性が低下し
、また錆、油脂、ペイント等によるピツトやブローホー
ルが発生し易くなる。
These have the function of reducing the amount of diffusible hydrogen in the weld metal and improving cracking resistance, as well as preventing the formation of pits and blowholes caused by rust, oil, fat, paint, etc. attached to the surface of the base metal. If it is less than 3%, the above-mentioned functions will not be exhibited significantly, and cracking resistance will decrease due to an increase in the amount of diffusible hydrogen, and pits and blowholes due to rust, oil, paint, etc. will be likely to occur.

一方15%を越えると、スラグの流動性が増大して凸ビ
ードになり易く等脚性も損なわれる。5MgC03:5
〜25% MgCO3はガス発生剤として作用し、大気から溶接金
属を保護する為の成分である。
On the other hand, if it exceeds 15%, the fluidity of the slag increases, making it easy to form convex beads and impairing isopodal properties. 5MgC03:5
~25% MgCO3 acts as a gas generating agent and is a component for protecting the weld metal from the atmosphere.

アーク熱による分解後スラグに移行するMgOが作業性
を劣化させない。MgCO3が5%未満では、CO2ガ
スの発生量が少なすぎてシールド不良が起リピツトが発
生し易くなると共に、窒素ガスの吸収によつて溶接金属
の靭性が劣化する。一方25%を越えると、CO2ガス
の発生量は充分であるが、アークが不安定になつてアー
ク切れ現象が多発しアンダーカツト等の継手欠陥が生じ
易くなると共に、スラグの粘性が増大して被包性が低下
しビードが凸状になる。DFe及び/又はMnの酸化物
:2〜10%具体例としてはFeO,.Fe2O3、M
nOlMnO2等が挙げられ、これらは何れも同効物質
であるから単独で或は2種以上を適宜組み合わせて使用
できる。
MgO transferred to slag after decomposition due to arc heat does not deteriorate workability. If MgCO3 is less than 5%, the amount of CO2 gas generated is too small, causing shield failure and causing repeat pits, and the toughness of the weld metal deteriorates due to absorption of nitrogen gas. On the other hand, if it exceeds 25%, the amount of CO2 gas generated is sufficient, but the arc becomes unstable and arc breakage occurs frequently, joint defects such as undercuts are likely to occur, and the viscosity of the slag increases. The encapsulation property decreases and the bead becomes convex. DFe and/or Mn oxide: 2 to 10% Specific examples include FeO, . Fe2O3, M
nOlMnO2, etc., and since all of these have the same effect, they can be used alone or in an appropriate combination of two or more.

これら酸化物に含まれる酸素は、溶融金属中の炭素との
反応によつてCOガス又はCO2ガスを発生し、多孔質
の溶融スラグを生成するので、これらは以後酸化性酸化
物という。その結果スラグの見掛け体積が増大し、スラ
グの被包性が大幅に改善され美麗なビード形状が約束さ
れる。これらの効果を有意に発揮させる為には2%以上
の添加が必要であり、2%未満では見掛けスラグ量の不
足によつて凸ビードが形成され易く、また被包性の低下
によつてアンダーカツト等を起こし易くなる。一方10
%を越えると、見掛けスラグ量が増大しすぎる為にスラ
グの先行及び2段ビードの問題を惹起し、且つ酸素過剰
になつて脱酸不足によるブローホール発生を招く。う
Mn:2〜10% 金属Mn或はフエロマンガン等として配合され、脱酸剤
としての機能と合金元素としての機能を併有している。
Oxygen contained in these oxides generates CO gas or CO2 gas by reaction with carbon in the molten metal, producing porous molten slag, and therefore these are hereinafter referred to as oxidizing oxides. As a result, the apparent volume of the slag increases, the encapsulation of the slag is greatly improved, and a beautiful bead shape is guaranteed. In order to exhibit these effects significantly, it is necessary to add 2% or more; if it is less than 2%, convex beads are likely to be formed due to a lack of apparent slag amount, and underfilling may occur due to a decrease in encapsulation. It becomes easy to cause cuts, etc. On the other hand 10
If it exceeds %, the apparent amount of slag increases too much, causing problems of leading slag and two-stage beads, and excess oxygen, leading to the generation of blowholes due to insufficient deoxidation. cormorant
Mn: 2-10% Mn is blended as metal Mn or ferromanganese, and has both the function as a deoxidizing agent and the function as an alloying element.

しかし本発明の様な高張力鋼溶接用低水素系溶接棒にあ
つては、溶接金属の機械的性質を改善する為の合金元素
としての役割りが強い。2%未満では溶接金属の機械的
性質(衝撃強度、伸び率、しぼり特性等)を十分に改善
できず、高張力鋼溶接用としての適性を満足できない。
However, in the case of a low-hydrogen welding rod for high-strength steel welding as in the present invention, it plays a strong role as an alloying element for improving the mechanical properties of the weld metal. If it is less than 2%, the mechanical properties (impact strength, elongation, squeezing properties, etc.) of the weld metal cannot be sufficiently improved, and the suitability for welding high-strength steel cannot be satisfied.

一方10%を越えると高温割れ性が低下する。8Si.
Mg.A1、Tiの1種以上:0.5〜8%金属粉或は
フエロアロィ等の合金粉として配合され、強力な脱酸作
用を有している。
On the other hand, if it exceeds 10%, hot cracking properties will decrease. 8Si.
Mg. One or more of A1 and Ti: 0.5 to 8% It is blended as metal powder or alloy powder such as ferroalloy, and has a strong deoxidizing effect.

脱酸作用はMnよりも強力であるから、Mnとの共存下
ではこれらの元素が脱酸剤として作用し、溶接金属中へ
のMnの歩留りを高める。0.5%未満では脱酸不足に
よつてブローホールが発生し易くなるほか溶接金属への
Mnの歩留りも低下する。
Since the deoxidizing effect is stronger than that of Mn, these elements act as deoxidizing agents when coexisting with Mn, increasing the yield of Mn in the weld metal. If it is less than 0.5%, blowholes tend to occur due to insufficient deoxidation, and the yield of Mn in the weld metal also decreases.

一方8%を越えると、CO及びCO2ガスを発生させる
為の酸素が消費され、見掛けのスラグ量が不足して被包
性が劣化しアンダーカツトが発生し易くなる。このほか
被覆剤中に必要に応じて適量の鉄粉を配合すれば、アー
ク安定性が向上すると共に溶着金属量の増大によつて溶
接能率を高めることができるので好ましい。
On the other hand, if it exceeds 8%, oxygen for generating CO and CO2 gas will be consumed, the apparent amount of slag will be insufficient, the encapsulation will deteriorate, and undercuts will likely occur. In addition, it is preferable to incorporate an appropriate amount of iron powder into the coating material, if necessary, because it improves arc stability and increases welding efficiency by increasing the amount of deposited metal.

しかし鉄粉量が多すぎるとアークの広がり及び吹き付け
強さが劣化し、且つスラグの被包性が低下して凸ビード
になり易くなるので、60%以下に止めるべきである。
ところで本発明では前記6、7、8で説明した様に、酸
化性酸化物(Fe.Mn酸化物)と脱酸成分(Si.M
g.Al、Ti及びMnの一部)の含有量を特定するこ
とが不可欠の要件であるが、適正なビード形状を確保す
る為には酸化性酸化物中の酸素と脱酸成分の量の均衡を
考慮すべきであることが確認された。即ち脱酸成分が相
対的に少なすぎて酸素過剰の状態になると、見掛けのス
ラグ量が多くなりすぎて2段気昧の凸ビードが形成され
易くなり、一方酸素不足の状態では見掛けスラグ量が不
十分になつて単純な凸ビードが形成される。そこで酸化
性酸化物と脱酸成分との量的均衡の適正範囲を確保すべ
く、下記の確認実験を行なつた。即ちFe及びMnの酸
化物についてはほぼ全量が酸化性酸化物として作用する
から、酸化性酸化物(Y)の含有率はとし、また脱酸成
分のうちSi,.Mg,.Al,.Tiはほぼ全量が脱
酸剤として作用し、Mnは4/5量が溶接金属中に歩留
り1/5量が脱酸剤として消費されるから、脱酸成分(
X)はとし、被覆剤中のXとYがビード形状に及ぼす影
響を調べた。
However, if the amount of iron powder is too large, the spread of the arc and the blowing strength will deteriorate, and the encapsulation of the slag will decrease, making it easier to form convex beads, so it should be kept at 60% or less.
By the way, in the present invention, as explained in 6, 7, and 8 above, an oxidizing oxide (Fe.Mn oxide) and a deoxidizing component (Si.Mn oxide) are used.
g. Although it is essential to specify the content of Al, Ti, and some of Mn), it is necessary to balance the amount of oxygen in the oxidizing oxide and the deoxidizing component to ensure a proper bead shape. It was confirmed that this should be considered. In other words, if the deoxidizing component is relatively too small and there is an excess of oxygen, the apparent amount of slag becomes too large and two-stage convex beads are likely to be formed.On the other hand, if there is a lack of oxygen, the apparent amount of slag It becomes insufficient and a simple convex bead is formed. Therefore, in order to ensure an appropriate range of quantitative balance between the oxidizing oxide and the deoxidizing component, the following confirmation experiment was conducted. That is, since almost all of the oxides of Fe and Mn act as oxidizing oxides, the content of oxidizing oxides (Y) is set at a certain level, and among the deoxidizing components, Si, . Mg,. Al,. Almost all of Ti acts as a deoxidizing agent, and 4/5 of Mn is retained in the weld metal and 1/5 is consumed as a deoxidizing agent.
X) was used to examine the effects of X and Y in the coating on the bead shape.

結果を第1図に示す。The results are shown in Figure 1.

但し実験条件及び判定基準は下記の通りとした。〔実験
条件] 他の被覆剤成分:(配合比率) 心線:軟鋼、5.5mm(I)X7OOmml被覆率:
約43%試験板:12t×100W×7501(M77
!)、SM5OA(C=0.39%)表面に20μのウ
オツシユプライマ一塗布継手形状:第2図参照 溶接法:グラビテイ一溶接、運棒比1.2倍溶接電流:
A.C.24OA〔判定基準〕 ○:フラツトで良好なビード(第3図参照)X:2段気
昧の凸ビード(第4図参照)又は単純な凸ビード(第5
図参照)△:上記○と×の中間的形状 第1図の結果からも明らかな様に、X.!l:.Yの値
が夫々本発明の要件を満たしていても、Y値が(X/2
+6)の値を越えるとビード形状が悪化し、また(X/
2−1)の値未満であつても矢張り良好なビード形状は
得られない。
However, the experimental conditions and criteria were as follows. [Experimental conditions] Other coating components: (mixing ratio) Core wire: Mild steel, 5.5 mm (I) x 7 OO mml Coverage rate:
Approximately 43% test board: 12t x 100W x 7501 (M77
! ), SM5OA (C=0.39%) 20 μ of wash primer applied to the surface Joint shape: See Figure 2 Welding method: Gravity welding, rod operation ratio 1.2 times Welding current:
A. C. 24OA [Judgment Criteria] ○: Flat and good bead (see Figure 3)
(See figure) △: Intermediate shape between the above ○ and × As is clear from the results in Fig. 1, X. ! l:. Even if each value of Y satisfies the requirements of the present invention, the Y value is (X/2
If the value exceeds +6), the bead shape will deteriorate;
Even if the value is less than 2-1), a consistently good bead shape cannot be obtained.

しかしY値が(X/2+6)と(X/2−1)の範囲内
となる様に配合量を設定すると、フラツトで等脚性の優
れた美麗なビードを確実に得ることができる。本発明は
概略以上の様に構成されており、被覆剤の成分組成を前
述の如く特定することによつて、優れた溶接作業性(ア
ーク安定性、スラグ剥離性等)を確保しつつ、ペイント
等に起因するブローホールをはじめとしてピツトやアン
ダーカツト等の欠陥を可及的に防止し得ることになつた
。しかも本発明の溶接棒を使用すれば溶接金属自体の機
械的性質が改善されると共に、フラツトで等脚性の優れ
た溶接ビードを確実に得ることができ、特に高張力鋼用
低水素系被覆アーク溶接棒としての実用的価値は頗る大
きい。次に本発明の実施例を示す。
However, by setting the blending amount so that the Y value falls within the range of (X/2+6) and (X/2-1), it is possible to reliably obtain a beautiful bead that is flat and has excellent isopodal properties. The present invention is roughly constructed as described above, and by specifying the component composition of the coating material as described above, it is possible to ensure excellent welding workability (arc stability, slag removability, etc.) and This makes it possible to prevent defects such as blowholes, pits, and undercuts as much as possible. Furthermore, by using the welding rod of the present invention, the mechanical properties of the weld metal itself are improved, and a weld bead with excellent flat and isolateral properties can be reliably obtained. Its practical value as an arc welding rod is extremely large. Next, examples of the present invention will be shown.

実施例 第1表に示す成分組成の被覆剤原料を適量の水ガラス系
粘結剤と混練し、これを5.5mm(!)X7OOmm
l又は4.0mmφ×400mm1の軟鋼心線に塗布し
て被覆アーク溶接棒を製造し、各溶接棒について溶接作
業性(アーク安定性、スラグ被包性、ビード形状、アン
ダーカツト)、耐ペイント性(ピツト)、拡散性水素量
及び耐割れ性を試験した。
Example A coating material raw material having the composition shown in Table 1 was kneaded with an appropriate amount of water glass binder, and this was mixed into a 5.5 mm (!) x 7 OO mm.
A coated arc welding rod is manufactured by coating a mild steel core wire of 1 or 4.0 mmφ x 400 mm 1, and each welding rod is tested for welding workability (arc stability, slag encapsulation, bead shape, undercut) and paint resistance. (Pitt), diffusible hydrogen amount and cracking resistance were tested.

尚耐ペイント性、拡散性水素量及び耐割れ性は下記の方
法で試験した。〔耐ペイント性〕 供試棒:5.5mmφ×700mu1 試験板:12t×100W×7501(Mm)、SM5
OA(C=0.39%)表面に20μのウオツシユプラ
イマ一塗布継手形状:第2図参照、セカンド側のビード
で耐ペイント性を判定溶接電流:A.C.24OA 溶接法:グラビテイ一溶接、運棒比1.2倍(n一3)
〔拡散性水素量]・・・・・・・・・JIS−Z−31
13供試棒:4.0m71L(!)X4OOm7!Ll
溶接電流:A.C.l75A溶接法:手溶接 運棒比:ビード長115mm/使用棒長150mm〔耐
割れ性](JIS−Z−3157、U型スリツト溶接割
れ試験)供試棒:4.0mm(!)X4OOmml溶接
電流:A.C.l8OA 溶接法:手溶接 運棒比:ビード長60mm/使用棒長75門1試験板:
19t×150W×2001(M7!t)、SM5OA
(C−0.41%)試験温度:R.T.(約26〜30
℃) 結果を第2表に示す。
The paint resistance, diffusible hydrogen content, and cracking resistance were tested using the following methods. [Paint resistance] Test bar: 5.5mmφ x 700mu1 Test plate: 12t x 100W x 7501 (Mm), SM5
OA (C=0.39%) Apply 20μ of wash primer to the surface. Joint shape: See Figure 2. Paint resistance determined by bead on second side. Welding current: A. C. 24OA Welding method: gravity welding, rod operation ratio 1.2 times (n-3)
[Diffusible hydrogen amount]...JIS-Z-31
13 Test rod: 4.0m71L(!)X4OOm7! Ll
Welding current: A. C. 175A welding method: Manual welding Rod operation ratio: Bead length 115 mm / Rod length used 150 mm [Crack resistance] (JIS-Z-3157, U-type slit weld cracking test) Test rod: 4.0 mm (!) x 4 OO mml Welding current :A. C. 18OA Welding method: Manual welding Rod operation ratio: Bead length 60mm/Used rod length 75 gates 1 test plate:
19t x 150W x 2001 (M7!t), SM5OA
(C-0.41%) Test temperature: R. T. (about 26-30
℃) The results are shown in Table 2.

第1、2表より次の様に考察することができる。From Tables 1 and 2, the following considerations can be made.

(1) A6.l及び2は市販されているすみ肉溶接用
低水素系被覆アーク溶接棒の代表例で、溶接作業性が良
好なもの(腐1)は継手性能が悪く、継手性能を改善し
たもの(A6.2)は溶接性が劣悪である。(2) /
F6lO〜21は本発明で規定する要件の何れかを欠除
する比較例で、以下に示す如く本発明の目的を達成でき
ない。
(1) A6. 1 and 2 are representative examples of commercially available low-hydrogen-based coated arc welding rods for fillet welding.The one with good welding workability (A6.1) has poor joint performance, and the one with improved joint performance (A6. 2) has poor weldability. (2) /
F61O-21 are comparative examples that lack any of the requirements defined by the present invention, and cannot achieve the purpose of the present invention as shown below.

腐10:MgCO3量が不足する為シールド不良が起こ
り、ピツト数が多発する。
Corrosion 10: Due to insufficient amount of MgCO3, shield failure occurs and the number of pits increases.

腐11:MgCO3の不足分をCacO3で補なつたも
のであるが、スラグ被包性が悪くビード形状が悪化(凸
ビード)する。
Corrosion 11: The lack of MgCO3 was supplemented with CacO3, but the slag encapsulation was poor and the bead shape deteriorated (convex bead).

滝12:MgCO3量が多すぎる為アーク安定性が低下
し、アーク切れにより作業性が悪い。
Waterfall 12: Arc stability deteriorates due to too large amount of MgCO3, and workability deteriorates due to arc breakage.

滝13:SiO2量が不足する為スラグの流動性が不安
定になり、凸ビードが形成される。滝14:金属フツ化
物量が不足する為、耐ペイント性及び耐割れ性を満足で
きない。
Waterfall 13: Due to insufficient amount of SiO2, the fluidity of the slag becomes unstable and convex beads are formed. Waterfall 14: Due to insufficient amount of metal fluoride, paint resistance and cracking resistance cannot be satisfied.

./F6.l5:金属フツ化物量が多すぎる例で、耐ペ
イント性及び耐割れ性は良好であるものの溶接作業性が
劣悪である。
.. /F6. 15: An example in which the amount of metal fluoride is too large, and although paint resistance and cracking resistance are good, welding workability is poor.

./F6.l6:SiO2量が多すぎる為溶接作業性が
悪く、またスラグ剥離性も悪い。
.. /F6. 16: Because the amount of SiO2 is too large, welding workability is poor and slag removability is also poor.

滝17:Fe、Mnの酸化物量が多すぎる為見掛けスラ
グ量が増加し、安定したスラグ被包性が得られずビード
形状及びアンダーカツトの面で問題がある。
Waterfall 17: Because the amount of oxides of Fe and Mn is too large, the apparent amount of slag increases, and stable slag envelopment cannot be obtained, causing problems in terms of bead shape and undercut.

廃18:脱酸剤が多すぎる為に見掛けのスラグ量が少な
く、スラグ被包性の低下によりビードが凸気味になる。
Waste 18: Due to too much deoxidizing agent, the apparent amount of slag is small, and the bead becomes slightly convex due to a decrease in slag envelopment.

滉19:酸化性酸化物量が少ない為にスラグの見掛けス
ラグ量を十分に高めることができず、ビードが凸気昧に
なる。
滉19: Since the amount of oxidizing oxides is small, the apparent amount of slag cannot be sufficiently increased, and the beads become convex.

A62O:各配合成分の含有率は本発明の要件を満足す
るが、前述のY値が(X/2+6)値を越える比較例〔
Y=8.5%、(X/2+6)一8.1%〕で、酸化性
酸化物と脱酸剤とのバランスが悪く、見掛けのスラグ量
が多すぎる為に2段気昧の凸ビードになる。
A62O: Comparative example in which the content of each compounded component satisfies the requirements of the present invention, but the above-mentioned Y value exceeds (X/2+6) value [
Y=8.5%, (X/2+6)-8.1%], the balance between oxidizing oxide and deoxidizing agent is poor, and the apparent amount of slag is too large, resulting in a two-stage convex bead. become.

滝21:Y値が(X/2−1)値未満である比較例〔Y
=2.5%、(X/2−1)=3.3%]で、見掛けス
ラグ量が不足する為単純な凸ビードが形成される。
Waterfall 21: Comparative example where the Y value is less than the (X/2-1) value [Y
= 2.5%, (X/2-1) = 3.3%], a simple convex bead is formed because the apparent slag amount is insufficient.

(3)磨3〜9は何れも本発明の要件を充足する実施例
で、溶接作業性及び継手性能共に極めて優れている。
(3) Polishing Nos. 3 to 9 are all examples that satisfy the requirements of the present invention, and are extremely excellent in both welding workability and joint performance.

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

第1図は、ビード形状に及ぼす酸化性酸化物含有量(Y
)と脱酸成分含有量(X)の関係を示すグラフ、第2図
は、耐ペイント性試験で採用した継手形状を示す要部見
取り図、第3〜5図はビード形状の判定基準を示す概略
図である。
Figure 1 shows the effect of oxidizing oxide content (Y
) and deoxidizing component content (X), Figure 2 is a sketch of the main parts showing the joint shape adopted in the paint resistance test, and Figures 3 to 5 are schematic diagrams showing the criteria for determining bead shape. It is a diagram.

Claims (1)

【特許請求の範囲】 1 MgO:5〜24%、TiO_2:6〜25%、S
iO_2:3〜20%、金属フッ化物:3〜15%、C
O_2をMgCO_3の形でMgCO_3に換算して5
〜25%、Fe及び/若しくはMnの酸化物:2〜10
%、Si、Mg、Al及びTiから選択される1種以上
の元素:0.5〜8%、Mn:2〜10%を夫々含み、
且つ(Fe酸化物及びMn酸化物)の含有量をY%、〔
(Si、Mg、Al、Ti)+1/5Mn〕で与えられ
る含有量をX%とした場合のXとYの関係が次式を満足
する被覆剤を、(X/2−1)≦Y≦(X/2+6)固
着剤と混練し鋼心線に塗布したものであることを特徴と
する低水素系被覆アーク溶接棒。
[Claims] 1 MgO: 5-24%, TiO_2: 6-25%, S
iO_2: 3-20%, metal fluoride: 3-15%, C
Converting O_2 to MgCO_3 in the form of MgCO_3 is 5
~25%, Fe and/or Mn oxide: 2-10
%, one or more elements selected from Si, Mg, Al and Ti: 0.5 to 8%, Mn: 2 to 10%, respectively,
And the content of (Fe oxide and Mn oxide) is Y%, [
When the content given by (Si, Mg, Al, Ti) + 1/5Mn] is set to X%, the relationship between X and Y satisfies the following formula: (X/2-1)≦Y≦ (X/2+6) A low hydrogen-based coated arc welding rod, which is kneaded with a fixing agent and applied to a steel core wire.
JP5001980A 1980-04-14 1980-04-14 Low hydrogen coated arc welding rod Expired JPS5914315B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP5001980A JPS5914315B2 (en) 1980-04-14 1980-04-14 Low hydrogen coated arc welding rod

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP5001980A JPS5914315B2 (en) 1980-04-14 1980-04-14 Low hydrogen coated arc welding rod

Publications (2)

Publication Number Publication Date
JPS56144895A JPS56144895A (en) 1981-11-11
JPS5914315B2 true JPS5914315B2 (en) 1984-04-04

Family

ID=12847277

Family Applications (1)

Application Number Title Priority Date Filing Date
JP5001980A Expired JPS5914315B2 (en) 1980-04-14 1980-04-14 Low hydrogen coated arc welding rod

Country Status (1)

Country Link
JP (1) JPS5914315B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04116111U (en) * 1991-03-26 1992-10-16 太陽誘電株式会社 linearity coil

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP7039374B2 (en) * 2018-04-11 2022-03-22 日鉄溶接工業株式会社 Shielded metal arc welding rod for low hydrogen fillet welding
JP7440325B2 (en) * 2020-03-31 2024-02-28 Maアルミニウム株式会社 Aluminum brazing sheet for flux-free brazing

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH04116111U (en) * 1991-03-26 1992-10-16 太陽誘電株式会社 linearity coil

Also Published As

Publication number Publication date
JPS56144895A (en) 1981-11-11

Similar Documents

Publication Publication Date Title
JPS5915756B2 (en) Flux-cored wire for gas shield arc welding
KR20030021397A (en) Basic flux cored wire
KR100436489B1 (en) Flux cored wire for gas shielded arc welding of high tensile strength steel
JPS5913955B2 (en) Composite wire for stainless steel welding
JPS5914315B2 (en) Low hydrogen coated arc welding rod
CN102019519B (en) Welding stick filled with flux for welding
JP2001205483A (en) Flux-cored wire for gas shielded arc welding
JP2018114515A (en) Coated electrode for low hydrogen type fillet welding
JPH0335033B2 (en)
JP4311888B2 (en) Low hydrogen coated arc welding rod
JPH03285793A (en) Low hydrogen type coated arc welding electrode
JPH11216593A (en) Low hydrogen coated arc welding rod
JPS63199093A (en) Arc welding electrode coated on stainless core wire
JP7346328B2 (en) Low hydrogen coated arc welding rod for horizontal fillet welding
CN118977012B (en) Application of flux-cored wire for Q345qD steel in steel bridge U-rib upward internal welding
JP3577995B2 (en) Manufacturing method of fired flux for submerged arc welding
JPS58116990A (en) Flux for submerged arc welding
JP7752917B2 (en) Covered metal arc welding electrodes for galvanized steel sheets
JP2021049576A (en) Iron powder low-hydrogen type coated electrode
JPH01138098A (en) Coated electrode for stainless steel
JPS59110495A (en) Low hydrogen type coated arc welding electrode for fillet welding
JPH04356397A (en) Self-shielded arc welding composite wire
JPS591513B2 (en) Melting type flux for submerged arc welding
JPS58196195A (en) Baked flux for horizontal fillet submerged arc welding
JPH05293690A (en) Low-hydrogen type coated electrode for weather resistant steel