JPS58209499A - Low hydrogen covered arc welding rod - Google Patents

Low hydrogen covered arc welding rod

Info

Publication number
JPS58209499A
JPS58209499A JP9374782A JP9374782A JPS58209499A JP S58209499 A JPS58209499 A JP S58209499A JP 9374782 A JP9374782 A JP 9374782A JP 9374782 A JP9374782 A JP 9374782A JP S58209499 A JPS58209499 A JP S58209499A
Authority
JP
Japan
Prior art keywords
atomized
low hydrogen
welding rod
welding
arc welding
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
JP9374782A
Other languages
Japanese (ja)
Other versions
JPH0150519B2 (en
Inventor
Tomoyuki Abe
知之 阿部
Shozo Naruse
成瀬 省三
Naoki Yamanochi
山ノ内 直己
Seijiro Miura
三浦 精二郎
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 JP9374782A priority Critical patent/JPS58209499A/en
Publication of JPS58209499A publication Critical patent/JPS58209499A/en
Publication of JPH0150519B2 publication Critical patent/JPH0150519B2/ja
Granted legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/36Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
    • B23K35/365Selection of non-metallic compositions of coating materials either alone or conjoint with selection of soldering or welding materials

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Nonmetallic Welding Materials (AREA)

Abstract

PURPOSE:To stabilize an arc and to reduce spatters, by compounding fine particulate Fe-Mn, Fe-Si in a coating flux of a low hydrogen covered electrode thereby changing the droplet transfer in arc welding to spray transfer. CONSTITUTION:A flux of the compsn. consisting essentially of 1-25% SiO2, 0.5-20% TiO2, 12-60% carbonate such as CaCO3, MgCO3 or the like and 1- 25% fluoride such as CaF2, and contg. 1 or 2 kinds of 1-18% atomized Fe- Mn and 3-23% atomized Fe-Si of which >=55% has <=60 mesh grain sizes and <=45% iron powder is used as a coating material for a low hydrogen covered electrode. The electrode has good arc stability in the welding operation, produces less spatters per length of the electrode and forms excellent welding beads.

Description

【発明の詳細な説明】 本発明は、溶接作業特性の改祷された低水素系被覆アー
ク溶接棒に関し、特忙溶接アークのスプレー移行及び低
スパツタ等の特性を発揮する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 with improved welding properties, and relates to a low-hydrogen coated arc welding rod that exhibits properties such as spray transfer of a busy welding arc and low spatter. It's about sticks.

低水素糸′Ml覆アーク浴接棒(以下単に低水素糸溶接
棒という)は1機械的性質や耐割れ性能の良い♂接金属
を与えるものであるから、厚板や拘束力の大きい箇所に
おける溶接材料として汎用されてhる1、シかしイルミ
ナイト系やライムチタニア系等の一般溶接棒に比べて非
能率的であるということが指摘されている。その原因と
しては、被覆剤組成の違いもさることながら、被覆剤に
由来しして発生するシールドガスの違いによるところが
大きいとされて込る。即ち一般溶接棒におりて発生する
シールドガスの組成は、N2.N20.■等が主流を占
めているのでアークの安定性が良好であるのに対、して
、低水素系溶接棒ではCOやCO2が主流を占めるので
アークの安定性が悪くなるという煩向がある。又低水累
系の溶接棒では溶滴が大きくなってグロビュラ移行や短
絡移行や様相を呈し易(な9.使用棒長当りのスパッタ
発生倉が多くなって溶接作業性を著しく阻害するという
欠点があった。
Low-hydrogen yarn 'Ml arc-covered welding rod (hereinafter simply referred to as low-hydrogen yarn welding rod) provides a male weld metal with good mechanical properties and crack resistance, so it is suitable for thick plates and places with large binding force. Although it is widely used as a welding material, it has been pointed out that it is inefficient compared to general welding rods such as silica illuminite and lime titania. The reason for this is believed to be not only the difference in the composition of the coating material, but also the difference in the shielding gas generated from the coating material. That is, the composition of the shielding gas generated by a general welding rod is N2. N20. (2) etc. are the mainstream, resulting in good arc stability, whereas with low-hydrogen welding rods, CO and CO2 are the mainstream, resulting in poor arc stability. . In addition, welding rods with a low water composition tend to have large droplets that cause globular migration or short-circuit migration (9. The drawback is that the number of spatter generation chambers increases per length of the rod used, which significantly impedes welding workability. was there.

本発明はこの様な状況を憂慮してなされたものであって
、溶滴移行のスプレー化及びスパッタの減少を実現する
ことができる様な低水素系R1接棒の提供を目的とする
ものである。
The present invention was made in consideration of this situation, and aims to provide a low-hydrogen R1 contact rod that can realize spraying of droplet transfer and reduction of spatter. be.

上記目的を達成し得た本発明の低水素系溶接棒とは、ス
リブ形成剤、ガス発生剤等からなる7ラックス成分を固
着剤と共に鋼IL)線に塗着せしめたものにおいて、該
7ワツクスとして、 S i02 : 1〜25優(車量ヂ、以下同じ)Ti
02:O,F+〜20チ 次酸塩:12〜60係 金属弗化物:1〜25チ を含有し、更に アトマイズFe−8i:8〜28チ の1種又は2種以上を富有し、且つ全アトマイズ粉粒体
の55係以上が60メツシュ通過の細粒よシ構成される
ものを用いる点に要旨が仔在する、。
The low-hydrogen welding rod of the present invention that has achieved the above object is one in which a 7-lux component consisting of a rib forming agent, a gas generating agent, etc. is applied to a steel wire along with a bonding agent. As, Si02: 1 to 25 Yu (vehicle volume, the same below) Ti
02: Contains O,F+~20 thionic acid salt: 12~60 group metal fluoride: 1~25 thi, further enriched with one or more types of atomized Fe-8i: 8~28 thi, and The key point is to use a material in which 55 or more of the total atomized powder particles are composed of fine particles that pass through 60 meshes.

5j02.TiO2,CaCO2,CaF2゜MgCO
3,BaCO3等を上記範囲と一部重複する範囲で含有
する低水素系溶接棒用被覆剤Mi Iii物は、例えば
特公昭55−42678号によって知られている。叉ア
トマイズ合金鋼粉(例えは7e−Mn 、 F e−5
i 、 pe −N i等)を含有する被覆剤を合金t
4心線の周囲に破覆して一般の被憶アーク溶接棒とする
ことは例えば特公昭54−80908号によって知られ
ている。、しかし前者の公報によって開示された低水素
系溶接棒は。
5j02. TiO2, CaCO2, CaF2゜MgCO
3. A low-hydrogen welding rod coating Mi III containing BaCO3 and the like in a range partially overlapping with the above range is known, for example, from Japanese Patent Publication No. 55-42678. Atomized alloy steel powder (for example, 7e-Mn, Fe-5
i, pe-Ni, etc.) as an alloy t
It is known, for example, from Japanese Patent Publication No. Sho 54-80908, that the welding rod is broken around four core wires to form a general arc welding rod. However, the low hydrogen welding rod disclosed by the former publication.

(IIF2の存仕によって溶融スラグの一瀦点が低下し
てヒユーム発生呈が増大するという知見に基づき、スワ
ブ融点向上効果のあるTiO2をCaF2に対して2倍
(7&量比)以上にするということを要点とするもので
ある。しかしその結果高融点スラグによる#接作業性の
低下という問題が発生し、S i O2、B Fh C
03、M g C03の各成分配合址を調整して折合点
を求めるというものであるから、フラックス原料選択の
自国度が減少するという欠点がめシ、又本発明の課鵜と
するアークの安定やスパッタの軽減については、見るべ
き成果がなく、特に報告されていない。他方後者の公報
に記載された発明は、アトマイズ合金鋼粉が球状を呈し
ていることを利用し、溶接棒の塗装作業における被覆剤
のすべり性を良好にして被覆剤の固着性を向上させたも
のであシ、アークの安定性との関係については、被覆剤
の餓小割れや脱落によるヱー7切れ等を防止するという
程度に過ぎなかった。
(Based on the knowledge that the presence of IIF2 lowers the melting point of molten slag and increases the appearance of fume generation, it was decided to increase the amount of TiO2, which has the effect of improving the swab melting point, by at least twice that of CaF2 (7 & amount ratio). However, as a result, a problem arises in that # contact workability is reduced due to high melting point slag, and S i O2, B Fh C
03, M g C03 to find a compromise point by adjusting the composition of each component, there is a drawback that the degree of selection of flux raw materials is reduced, and the stability of the arc, which is a problem of the present invention, is Regarding the reduction of spatter, there are no notable results and no particular report has been made. On the other hand, the invention described in the latter publication takes advantage of the spherical shape of atomized alloy steel powder to improve the slipperiness of the coating material in the coating process of welding rods, thereby improving the adhesion of the coating material. However, in terms of the relationship with arc stability, it was only effective at preventing the coating material from cracking or breaking due to falling off.

こ九た対し本発明は、T j O2とCaF2の配合比
、あるいはがば酸塩の種類等について原料選択の自由度
が制約されずKf4接作業性の同上を図ろうとするもの
であシ、特にアトマイズFfl−Mnやアトマイズpe
−5iによって溶滴移行状態を改善し、その効果として
アークの安定やスパッタの軽減を達成させようとするも
のである。そして七の為には全アトマイズ粉粒体の粒度
構成も重要な役割りを果しているということを知見し、
これら総合的考察の上に立って本発明を完成するに至っ
たものである9、従って本明細書においては、アトマイ
ズ粉粒体に関する点から睨明をはじめる。
In contrast, the present invention aims to achieve the same Kf4 contact workability without restricting the degree of freedom in selecting raw materials with respect to the blending ratio of Tj O2 and CaF2, the type of gabarate, etc. Especially atomized Ffl-Mn and atomized pe
-5i is intended to improve the droplet transfer state and achieve the effect of stabilizing the arc and reducing spatter. We also discovered that the particle size composition of all atomized powder particles plays an important role for the purpose of
The present invention was completed based on these comprehensive considerations.9 Therefore, in this specification, we will begin with a focus on the atomized powder and granules.

Fe−MnやFe−8iは低水素系溶接棒用被覆剤にお
いて汎用の脱酸剤である。しかし本発明者等は、その性
状、種類、倉等について種々の角度から再検討したとこ
ろ、アトマイズ法(水アトマイズ及びガスアトマイズの
如何は問わない)によって製造される粉粒欽のFe−M
n及びpe−siを、前者:1〜18φ、後者二3〜2
B俤の範囲で、且つ全アトマイズ粉粒体の55優以上が
60メツシュ通過の細粒より構成されたものを用いるこ
とが、アーク溶接時の溶滴移行状態をスプレー移行とし
、且つスパッタの発生を抑制する上で極めて重要である
ということが分かった。即ち第1,2表に示す組成の7
ラツクス成分に固着剤を加えて混線し、これを軟鋼、U
線の外周に塗布して試作溶接棒(4,0關φX40(1
mm’)を製令した1、石、3図に示す如く、円形銅板
(1800mmφ)1上に試験板(400g’X613
f7m”X 19”)2を乗せ、8fの前傾姿勢を保ち
ながら、長さ方向にビードオンプレート溶接を行なった
(AC。
Fe-Mn and Fe-8i are general-purpose deoxidizers in low-hydrogen coating materials for welding rods. However, the present inventors reexamined its properties, types, storage, etc. from various angles, and found that Fe-M powder particles produced by the atomization method (regardless of water atomization or gas atomization)
n and pe-si, the former: 1-18φ, the latter two 3-2
Using particles in the range of B 2 and in which 55 or more of the total atomized particles are composed of fine grains that pass through 60 meshes will cause the droplet transfer state during arc welding to be spray transfer, and will prevent the generation of spatter. It was found that this is extremely important in suppressing the That is, 7 of the composition shown in Tables 1 and 2.
A fixing agent is added to the lux component to mix wires, and this is mixed into mild steel and U.
Coat the outer periphery of the wire and make a prototype welding rod (4.0 mm φX40 (1
As shown in Figure 3, a test plate (400 g' x 613
F7m"X 19")2 was mounted, and bead-on-plate welding was performed in the length direction while maintaining a forward leaning posture of 8f (AC).

18(IA)、、押祠反l上の91七敗スパッタ請を1
刑定し。
18 (IA), 91 seven defeats sputter request on Oshikihani 1
Sentenced.

F e −M 1(5F e−5iのata及び含有i
tとの関係を求めたところ、第4.夕図に示す様な結果
が得られた1、同飛散スパッタ址は、溶接棒の矩位消費
長さく cyn )に対する捕集総軍量で現わした(以
下同じ)。
F e -M 1 (5F e-5i ata and content i
When we sought the relationship with t, we found that the fourth. The results shown in Figure 1 were obtained. The amount of scattered spatter was expressed as the total amount of collected spatter against the rectangular consumption length (cyn) of the welding rod (the same applies hereinafter).

これらの結果を見れば明白である様に、アトマイズFe
−Mn又はアトマイズpe−5iを配合したもの(・印
)では、通常粉砕品(○印)に比べてスパッタ捕集量が
顕著に少なくなっている。
As is clear from these results, atomized Fe
The amount of spatter collected is significantly smaller in those containing -Mn or atomized PE-5i (marked with *) than in the normally pulverized product (marked with ○).

しかしアトマイズFfl−Mnの含有量が1q6未満、
アトマイズpa−53の含有量が8俤未満のものではス
パッタ発生量の軽減効果が不十分であるだけでなく、前
者では溶接金属の靭性不良、後者では脱酸不足によるブ
ローホールの発生等という不具合が付加されるので、前
者は196以上、後者は8俤以上と、夫々の下限を定め
た。他方前者がIB優を越えると溶接金属が硬くなって
耐割れ性が低下し、又後者が28係を越えると溶接金属
の靭性が低下すると共に生成スラグの粘度が増大してビ
ード表面に峨しい凹凸が残る。その為前者は18係以下
、後者は28%以下と、夫々上限を定めた。
However, the content of atomized Ffl-Mn is less than 1q6,
If the content of atomized PA-53 is less than 8 yen, not only will the effect of reducing the amount of spatter be insufficient, but the former will cause problems such as poor toughness of the weld metal, and the latter will cause blowholes due to insufficient deoxidation. is added, so we set the lower limits for the former as 196 or more and for the latter as 8 or more. On the other hand, when the former exceeds IB Excellent, the weld metal becomes hard and the cracking resistance decreases, and when the latter exceeds 28, the toughness of the weld metal decreases and the viscosity of the generated slag increases, causing it to thicken on the bead surface. Unevenness remains. For this reason, upper limits have been set for the former to be 18% or less, and for the latter to be 28% or less.

尚第8表はF6−Mnやpe−5iの配合址と溶接作業
性の関係を示すグラフであシ、被億剤基本成分は、 CaCU3及びMgCO3: 50%、S j O2:
 2俤 ’I’ j 02 : 2%、C11F2二15係、そ
の他=2〜29係 とした。又第11ン1は同表の(A−1)〜(A−6)
を用いたときの溶接金属の物性、第2図は(B−1)〜
(B−6)を用いたときの吸収エネルギー(vEo:K
g−m)を示すものである。即ち(A−1)はアトマイ
ズFe−Mnが少ない為スパッタ量が多く、(A−6)
はアトマイズpe−Mnが多いため強度および硬さが過
大であった。
Table 8 is a graph showing the relationship between F6-Mn and PE-5i compounding material and welding workability.The basic components of the coating agent are: CaCU3 and MgCO3: 50%, SjO2:
2 'I' j 02: 2%, C11F2215 ratio, others = 2 to 29 ratio. Also, No. 11 is (A-1) to (A-6) in the same table.
The physical properties of weld metal when using , Figure 2 is (B-1)~
(B-6) Absorbed energy (vEo:K
g-m). That is, (A-1) has a large amount of sputtering due to less atomized Fe-Mn, and (A-6)
had excessive strength and hardness due to the large amount of atomized pe-Mn.

(B−1)はアトマイズFe−5iが少ない為スパッタ
量が多(、(B−6)はアトマイズFe−5iが多い為
靭性が低い。冑(A−2)〜(A−5)、(B−2) 
〜(B−5) 、 (C−1)〜(C−4> 、 (D
−t )〜(D−4)は本発明を満足する例である。
(B-1) has a large amount of spatter due to a small amount of atomized Fe-5i (, (B-6) has a low toughness due to a large amount of atomized Fe-5i. B-2)
~(B-5), (C-1)~(C-4>, (D
-t) to (D-4) are examples that satisfy the present invention.

+、a     R表 ft1IFeNiやFe−Mo等のFe合金は、元々配
合片が制限されて(例えば2係以下)bる為、アークの
スプレー化やスパッタの低減に寄与する効果は少ない。
+, a R Table ft1 Since Fe alloys such as FeNi and Fe-Mo are inherently limited in composition (e.g., coefficient 2 or less), they have little effect in contributing to reducing arc spray and spatter.

しかし本発明者等はこれに鵬足せず、溶滴の移行状態及
びスパッタの発生欺忙つぃて更に検討を重ねた結果、次
の様なことが分かった。即ちアトマイズF e−Mnや
アトマイズFT3−si等の粒子形状は、通常粉砕品と
異なって球状を呈するから、粒子間の空t*が比較的少
なく且つ一定である。。
However, the inventors of the present invention were not satisfied with this, and as a result of further investigation into the transfer state of droplets and the occurrence of spatter, they found the following. That is, since the particle shape of atomized Fe-Mn, atomized FT3-si, etc. exhibits a spherical shape unlike a normal pulverized product, the spaces t* between particles are relatively small and constant. .

その為W覆がアーク熱で溶融する過程及び溶融して母材
側へ移行する過程が極めて清らかになシ、上述のスプレ
ー移行形態が得られるのであるが、アトマイズの粒度分
布が大きくばらつくと、それらの効果が不安定になるだ
けでなく、被覆剤塗装上の問題も発生する。第4表は、
全アトマイズ粉粒体の粒度;4を変更させたときの溶接
試験結果を示方枦メであるが、全アトマイズ粉粒体の5
5チ以上が60メツシュ通過の細粒より構成される4の
(C−1〜5)では、溶滴の移行がスプレー伏であると
共にスパッタ発生@が■著に少なく、本発明の目的がほ
ぼ完全に達成されていた。一方これらの条件を満足しな
いもの(C・6〜8)は溶滴の移行が不連続であシ、瞬
間的には爆発移行を見せることがあシ、スパッタの多発
につながると共に、アークの集中性が悪くなるという欠
陥があった。この他、C・4〜5では若干ながら被覆の
脱落がみられ、この様な問題も回避しようとすiば、6
0メツシュ通過、200メツンユ非通過のものが全アト
マイズ粉粒体の40係以上を占めるもの(C−1〜8)
が最處当であるとの結論を得た。換言すると、アトマイ
ズ粉粒体について細目のものが多(なるにつれてスパッ
タが減少し、溶滴の移行が女定するカニ、被覆の密度が
過大になって塗装被覆剤の脱落が起シ易くなる。他方粗
目のものが多くなると、被覆剤中の空隙率が過大になっ
てアークの集中性が悪くなると共にスパッタも多発して
くる。間第4表における溶接作業試験の条件は次のte
lであシ、又スパッタの1審生景は第3図の方法に準じ
て測定した。
Therefore, the process in which the W coating is melted by arc heat and the process in which it melts and transfers to the base metal side is extremely clear, and the above-mentioned spray transfer form can be obtained. However, if the particle size distribution of the atomize varies greatly, Not only do their effects become unstable, but also problems arise when applying the coating. Table 4 is:
The particle size of all atomized powder and granules is shown as a welding test result when changing the particle size of 4.
In No. 4 (C-1 to C-5), in which 5 or more meshes are composed of fine grains that have passed through 60 meshes, the transfer of the droplets is spray-free and the generation of spatter is extremely small. It was completely accomplished. On the other hand, for those that do not satisfy these conditions (C 6 to 8), the transfer of droplets is discontinuous, and explosive transfer may occur instantaneously, leading to frequent spatter and concentration of arc. There was a defect that the sex became worse. In addition, a slight amount of shedding of the coating was observed in C.4 to C.5, and if you tried to avoid this problem,
Items that pass 0 mesh and do not pass 200 mesh account for 40 or more of the total atomized powder (C-1 to 8)
It was concluded that this is the most appropriate option. In other words, the finer the atomized powder is, the less spatter occurs, the transfer of droplets is affected, and the density of the coating becomes excessive, making it easy for the paint coating to fall off. On the other hand, if the number of coarse grains increases, the porosity in the coating material will become excessive, resulting in poor arc concentration and frequent spatter.The conditions for the welding work test in Table 4 are as follows:
The first appearance of spatter was measured according to the method shown in FIG.

〈浴接条件〉 試験板: 8M50 (12txts” X75*mW
X45 (Irprs’ )供試棒:4.0間φX40
01繍1 16接’rTl流二150〜170A 浴接姿勢:下向きビードオンプレート溶接(水平すみ肉
及び立向上進すみ肉) 次にアトマイズF e−Mu (F e−8厘)以外の
成分について説明する。
<Bath contact conditions> Test plate: 8M50 (12txts”X75*mW
X45 (Irprs') Test rod: φX40 between 4.0
01 Embroidery 1 16 contact'rTl flow 2 150-170A Bath contact position: Downward bead-on-plate welding (horizontal fillet and vertical fillet) Next, regarding components other than atomized Fe-Mu (Fe-8 Rin) explain.

S !02 : 1〜25ダ スラグ形by剤として大きな役割りを果すが、1係未満
ではスラグの彼包性が過大となってビードの波形が乱れ
、他方25チを越えるとスラグの神色性が過大になって
スラグがビードに食す込ミ易くなる。
S! 02: 1 to 25 das It plays a major role as a slag-type bying agent, but if it is less than 1 part, the envelopment of the slag becomes excessive and the waveform of the bead becomes disordered, while if it exceeds 25 parts, the divine color of the slag becomes excessive. This makes it easier for the slag to dig into the bead.

T io2: 0,5〜20チ ビード外観に羨しい光沢を与えるが、0.5係に満たな
いとその効果が発揮されず、逆に20チを越えるとスラ
グが轍密になシ通ぎて剥離性が悪くなる。
T io2: 0.5 to 20 inches It gives an enviable luster to the exterior, but if it is less than 0.5 inches, its effect will not be exhibited, and on the other hand, if it exceeds 20 inches, the slag will pass through the ruts tightly. Peelability deteriorates.

伏酸塩:12〜60係 ガス発生剤であシ、CB、Mg、Ba、Sr等の汰酸塩
として配合されるが、12チ未満ではガス発生iが少な
くなってシールド不足に基づくブローホールの発生が見
られ、他方60%を越えるとスラグが高塩基性となシ、
アーク吹きが弱くなって溶面速度の低下も招く。
Acid salts: 12 to 60 gas generating agents, which are blended as salts of CB, Mg, Ba, Sr, etc., but if less than 12, gas generation i decreases and blowholes occur due to insufficient shielding. On the other hand, if it exceeds 60%, the slag becomes highly basic.
The arc blow becomes weaker and the melting surface speed decreases.

金属弗化物:1〜25係 スリグ一点の61節によって流動性を調整する成分であ
シ、通常CaF2 s A lF 3 、 Na p等
として添加されるが、1チ未綿ではこの効果が発揮され
ない為にスラグの粘性が大きくなシ、凸形ビードになシ
易い。他方25係を越えると、スラグの流動性が過大と
なシ、良好なビード形状とはならない。
Metal fluoride: A component that adjusts fluidity by the 61 nodes of one slig of 1 to 25. It is usually added as CaF2sAlF3, Nap, etc., but this effect is not exhibited in 1-inch cotton. As a result, the slag has a high viscosity and tends to form convex beads. On the other hand, if it exceeds 25, the fluidity of the slag will be excessive and a good bead shape will not be obtained.

上記各成分の他にも、被覆剤における常用成分例えば合
金剤(Cu 、Ni 、Cr 、Mo 、Fe −7i
、Fe−A1.Mg等)、X9グ形成剤(A1203.
MgO,CaO,ZrO2,MnO等)、酸化剤(F 
eO@ F 8203等)等を配合することができるが
、特に鉄粉はRR効率を高める機能があル、推奨成分の
1つとして挙げられる。
In addition to the above-mentioned components, common components in coating materials such as alloying agents (Cu, Ni, Cr, Mo, Fe-7i
, Fe-A1. Mg, etc.), X9 group forming agent (A1203.
MgO, CaO, ZrO2, MnO, etc.), oxidizing agent (F
eO@F 8203, etc.), but iron powder in particular has the function of increasing RR efficiency and is listed as one of the recommended components.

しかし45チを越える倉の鉄粉を加えると、特に立面姿
勢溶接において溶接金属が垂れ落ち易くなるので、上限
は45係とする。
However, if more than 45 inches of iron powder is added, the weld metal tends to drip down, especially in vertical position welding, so the upper limit is set at 45 degrees.

本発明の被覆剤成分は、上記々述に従って選択の上配合
された組成物に、固着剤、好ましくは無磯固耀月(例え
ばS ! 02−K 20−H20。
The coating components of the present invention may be added to a composition selectively formulated in accordance with the above description, with a fixing agent, preferably a bonding agent (such as S!02-K20-H20).

5i02−Na20 1120,5j02−に20−N
 a 20  H20等)の水溶准を加えて混練される
。そしてこれを鋼心線の外周に塗イ’Ii L、た後、
高温焼成によって水分を可及的に完全に放出する。
5i02-Na20 1120, 20-N to 5j02-
a 20 H20 etc.) is added and kneaded. After applying this to the outer circumference of the steel core wire,
Moisture is released as completely as possible by high temperature firing.

本発明の低水素糸被覆棒は上記の如く構成されているの
で、溶滴の移行をスプレー状態に保持すると共に、スパ
ッタの発生量を大幅に減少せしめることができた。
Since the low hydrogen thread-coated rod of the present invention is constructed as described above, it is possible to maintain the transfer of droplets in a spray state and to significantly reduce the amount of spatter generated.

次に本発明の詳細な説明する。Next, the present invention will be explained in detail.

第6表に示す組成のフラックス成分に固着剤を加えて混
練し、これを・鋼心線に部製して4. OLlImφ×
400mm1の溶接棒を試作し、第6表に示す条件で#
接を行なって、溶接作業特性及びスパッタ発生量を測足
した。結果は第7表に示す。
A fixing agent is added to the flux components shown in Table 6 and kneaded, and this is made into a steel core wire.4. OLlImφ×
A 400mm1 welding rod was prototyped and #
Welding work characteristics and amount of spatter generation were measured. The results are shown in Table 7.

第5表に水式れる様にJ’・1〜8の本発明例では、本
発明における全条件力稲聞足されているから、第7表に
見られる如く全項目において良好な結果が得られている
。これに対しS−1〜12の各比較例は1本発明におけ
る条件のいずれかを満足してないので、不都合な結果し
か得られていない、。
As shown in Table 5, in the present invention examples of J'・1 to 8, all conditions of the present invention were applied, so as shown in Table 7, good results were obtained in all items. It is being On the other hand, each of Comparative Examples S-1 to S-12 did not satisfy any of the conditions of the present invention, and therefore only inconvenient results were obtained.

まずS・1.2は5102の配合割合が不適当である為
、スラグの被包性が不安定になってビード形状が悪い。
First, in S-1.2, the blending ratio of 5102 is inappropriate, resulting in unstable slag encapsulation and poor bead shape.

S・8はTlO2が過多である為スラグが緻密になって
剥離性が低下する。S・4゜5は炭酸塩の含有量が不適
正である為、S・4では溶接金属中にブローホールが発
生し、S・5ではアークの集中性が豊〈なっている。又
S・6゜7は金属弗化物の含有量が不適当である為、S
・6では凸ビードが形成され、S・7ではスラグの巻込
みが発生した。S・8のF e −M n &び、Fe
−5iは、通常粉砕品(前者はJIS−G2801相当
、後者はJIS−G2802相当)である為。
Since S.8 contains too much TlO2, the slag becomes dense and the releasability deteriorates. Since S.4.5 has an inappropriate carbonate content, blowholes occur in the weld metal in S.4, and arc concentration is increased in S.5. Also, S.6゜7 has an inappropriate content of metal fluoride, so S.
A convex bead was formed in S.6, and slag entrainment occurred in S.7. Fe −M n &amp; Fe of S・8
-5i is a normally crushed product (the former corresponds to JIS-G2801, the latter corresponds to JIS-G2802).

溶滴の移行がグロビュワー状となシ、スパッタの発生量
も少なくならなかった。S・9はアトマイズF 6−M
 t+の含有Mが少ない為、溶滴のスプレー移行が不安
定であシ、且つスパッタ減少率も低かった。S・10は
アトマイズpe−MnlアトマイズFe−5iがいずれ
も少ない例で、スパッタが減少しないだけでなく、溶接
金属中にブローホールが発生した。S・11.12はア
トマイズpe−8iの配合量が不適切である為5−11
ではブローホールが発生し、S・12ではビード表面に
凹凸が形成された。S・1・8はアトマイズ粉粒体の粒
度構成が不適当であった為、溶滴の移行状I!pが不連
続となシ、瞬間的に爆発移行を起こすことがあり、スパ
ッタ発生着の軽減に寄与するところも少なかった。
The transfer of the droplets was globular, and the amount of spatter generated did not decrease. S・9 is atomized F 6-M
Since the content of M in t+ was small, the spray transfer of droplets was unstable, and the spatter reduction rate was also low. S.10 is an example in which the amount of atomized pe-Mnl and atomized Fe-5i is small, and not only the amount of spatter is not reduced, but also blowholes are generated in the weld metal. S・11.12 is 5-11 because the amount of atomized PE-8i is inappropriate.
Blowholes occurred in the sample S.12, and irregularities were formed on the bead surface in the sample S.12. In S・1・8, the particle size structure of the atomized powder was inappropriate, so the droplet migration pattern I! If p is discontinuous, explosive transition may occur instantaneously, and there are few places that contribute to reducing spatter generation and deposition.

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

第1,2図はアトマイズFe−Mn、同Fe−51の効
果を示すグラフ、第8図は試験溶接の実施状況を示す断
面図、第4,5図はF e −M nとpe−5iの種
類と配合量によるスパッタ発生量の変化を示すグラフで
ある。 出願人  株式会社神戸製鋼所
Figures 1 and 2 are graphs showing the effects of atomized Fe-Mn and Fe-51, Figure 8 is a sectional view showing the implementation status of test welding, and Figures 4 and 5 are graphs showing the effects of atomized Fe-Mn and Fe-51. 3 is a graph showing changes in the amount of spatter generated depending on the type and blending amount. Applicant Kobe Steel, Ltd.

Claims (1)

【特許請求の範囲】 +l)スラグ形成剤、ガス発生剤等からなるフラックス
成分を固着剤と共に軟鋼心線に塗着せしめた低水素系被
覆アーク溶接棒において、前記フラックスはs io2
 : 1〜25チ(重量%、以下同じ)、rio2:o
、rv〜20チ、次酸塩:12〜60俤、金属弗化物:
1〜25チを必須成分として含有し、さらにアトマイズ
Fe−Mn:1〜18俤、アトマイズFe−8i:8〜
28係の1種または2棚を含有し、且つ全アトマイズ粉
粒体の55係以上が60メツシュ通過の細粒より横取さ
れ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。 (2、特許請求の範囲第1項において、全アトマイズ粉
粒体の40qb以上25に60メツシュ通過、200メ
ツシュ非通過の細粒より構成されたものである低水素系
被覆アーク溶接棒1、 (3)特許N1Ii求の範囲第1又は2項において、フ
ラックスは45係以下の鉄粉を含有するものである低水
素糸被覆アーク溶接棒1.
[Claims] +l) A low hydrogen-based coated arc welding rod in which a flux component consisting of a slag forming agent, a gas generating agent, etc. is applied to a mild steel core wire together with a fixing agent, wherein the flux is s io2
: 1 to 25 inches (weight%, same below), rio2:o
, rv ~ 20 t, subacid: 12 to 60 t, metal fluoride:
Contains 1 to 25 g as an essential component, and further contains atomized Fe-Mn: 1 to 18 g, atomized Fe-8i: 8 to
A low hydrogen-based coated arc welding rod containing one or two shelves of 28 meshes, and characterized in that 55 or more of the total atomized powder and granules are intercepted from fine grains passing through 60 meshes. (2. In claim 1, a low hydrogen-based coated arc welding rod 1 is composed of fine grains of 40 qb or more of all atomized powder particles passing through 25 to 60 meshes and not passing through 200 meshes, ( 3) In the scope of patent N1Ii, in item 1 or 2, the flux contains iron powder with a coefficient of 45 or less.1.
JP9374782A 1982-05-31 1982-05-31 Low hydrogen covered arc welding rod Granted JPS58209499A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP9374782A JPS58209499A (en) 1982-05-31 1982-05-31 Low hydrogen covered arc welding rod

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP9374782A JPS58209499A (en) 1982-05-31 1982-05-31 Low hydrogen covered arc welding rod

Publications (2)

Publication Number Publication Date
JPS58209499A true JPS58209499A (en) 1983-12-06
JPH0150519B2 JPH0150519B2 (en) 1989-10-30

Family

ID=14091010

Family Applications (1)

Application Number Title Priority Date Filing Date
JP9374782A Granted JPS58209499A (en) 1982-05-31 1982-05-31 Low hydrogen covered arc welding rod

Country Status (1)

Country Link
JP (1) JPS58209499A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07276083A (en) * 1994-03-31 1995-10-24 Kobe Steel Ltd Low hydrogen type coated electrode

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS548340A (en) * 1977-06-20 1979-01-22 Tatsuo Okazaki Transmission device of bicycle
JPS5775300A (en) * 1980-10-28 1982-05-11 Kobe Steel Ltd Low hydrogen type coated electrode
JPS5781997A (en) * 1980-11-07 1982-05-22 Kobe Steel Ltd Coated electrode containing low hydrogen

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS548340A (en) * 1977-06-20 1979-01-22 Tatsuo Okazaki Transmission device of bicycle
JPS5775300A (en) * 1980-10-28 1982-05-11 Kobe Steel Ltd Low hydrogen type coated electrode
JPS5781997A (en) * 1980-11-07 1982-05-22 Kobe Steel Ltd Coated electrode containing low hydrogen

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPH07276083A (en) * 1994-03-31 1995-10-24 Kobe Steel Ltd Low hydrogen type coated electrode

Also Published As

Publication number Publication date
JPH0150519B2 (en) 1989-10-30

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