JPS6129836B2 - - Google Patents
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- Publication number
- JPS6129836B2 JPS6129836B2 JP55151007A JP15100780A JPS6129836B2 JP S6129836 B2 JPS6129836 B2 JP S6129836B2 JP 55151007 A JP55151007 A JP 55151007A JP 15100780 A JP15100780 A JP 15100780A JP S6129836 B2 JPS6129836 B2 JP S6129836B2
- Authority
- JP
- Japan
- Prior art keywords
- coating
- welding
- bulk density
- slag
- shedding
- 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
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- Nonmetallic Welding Materials (AREA)
Description
本発明は被覆アーク溶接棒に関し、特に被覆の
保護筒としての機能を改善し、溶接作業性及び継
手性能を高めた被覆アーク溶接棒に関するもので
ある。
溶接能率及び継手性能を向上すべく種々の溶接
方法及び溶接材料が提案されている。しかしなが
ら溶接後の手直し(補修溶接)を含めた全溶接所
要時間の短縮及び継手性能の両面を満足するもの
は少ない。特にライム・チタニア系或はイルミナ
イト系等の被覆アーク溶接棒を用いた溶接におい
ては、溶接時間を短縮すべく高電流溶接を行なう
と被覆が焼けて脆くなり、溶接中に保護筒の一部
が脱落することがある。その為被覆の保護筒とし
ての機能が低下してシールド不足等が起こり、ブ
ローホール等の継手欠陥が発生するだけでなく作
業性が劣化する。その結果補修溶接が必要にな
り、溶接時間を短縮できない。
本発明者等は前述の様な事情に着目し、継手性
能を阻害することなく優れた溶接作業性が得られ
る様な被覆アーク溶接棒を開発すべく、被覆剤の
成分組成や被覆の物性等について研究を進めてき
た。本発明はかかる研究の結果完成されたもので
あつて、その構成とは、CaCO3及びMgCO3の1
種又は2種:7〜25%(重量%:以下同じ)、
TiO2:13〜40%及びSiO2:14〜33%を含有する
ライム・チタニア系又はイルミナイト系の被覆剤
を軟鋼心線外周に塗布し焼成した被覆アーク溶接
棒において、焼成後の被覆剤の嵩密度が2.1〜3.1
g/cm3であることを特徴とする溶接中の被覆の耐
脱落性の優れた被覆アーク溶接棒であるところに
要旨が存在する。
本発明では、被覆剤の成分組成を特定すると共
に、焼成後における被覆の嵩密度を特定範囲に設
定することによつて溶接中の被覆の脱落を防止
し、保護筒としての本来の機能を保持せしめるこ
とができた。その為補修溶接のいらない高品質の
溶接継手が作業性よく得られることになつた。
以下本発明における数値範囲設定の根拠を説明
する。
CaCO3及び/若しくはMgCO3:7〜25%
ガス発生剤として不可欠の成分であり、発生し
たガスによつて溶接金属を大気から保護する。7
%未満ではシールド不足となり、ブローホール等
の継手欠陥が生じ易くなり、一方25%を越えると
スラグの粘性が低下しビード形状が悪化する。こ
れらの作用からすれば両者は同効物質であるか
ら、一方を単独で使用してもよく或は適量ずつ併
用してもかまわない。通常は石灰、ドロマイト、
マグネサイト等として添加される。尚他の炭酸塩
例えばMnCO3やFeCO3等は、分解温度が低い為
に十分なシールド効果が得られない。但し少量を
CaCO3やMgCO3と併用することは差支えない。
TiO2:13〜40%
スラグに適度の被包性を与えるのに不可欠の成
分で、13%未満ではスラグの被包性が悪化しビー
ドが凸状化する。しかし40%を越えるとスラグの
剥離性が著しく悪化し、特に多層盛り溶接の作業
性が極端に悪くなる。原料としてはルチールやイ
ルミナイト等が用いられる。
SiO2:14〜33%
スラグの粘性調整剤として重要な成分であり、
14%未満では粘性不足によつてスラグの被包性が
不安定になり、且つビード形状も劣化する。また
33%を越えるととスラグがガラス状になり、剥離
が困難になる。原料としては珪砂、タルク、マイ
カ及びその他の珪酸塩が使用され、粘結剤として
使用される水ガラス中のSiO2も含まれる。
本発明では上記3成分を被覆剤の必須成分とす
るが、このほか必要に応じて下記の成分を配合す
ることもある。
鉄酸化物:FeO換算で3〜20%
鉄酸化物は母材に対する溶け込みを良くする作
用があり、特にイルミナイト系溶接棒の場合には
3%以上配合する必要がある。しかし多すぎると
アーク力が強くなりすぎてアンダーカツトを生じ
易くなるので、20%以下に止めねばならない。原
料としてはイルミナイト、砂鉄、スケール等が用
いられる。
鉄粉:40%以下
溶着金属量を増大し溶接能率を高める作用があ
る。しかし40%を越えると被覆の絶縁性が乏しく
なり、ビード形状も凸気味になるので好ましくな
い。尚Fe−MnやFe−Cr等のフエロアロイ中の
鉄も同効物質としての効果がある。
合金粉:5%以下
溶接金属の機械的性質や耐食性等を改善する為
に、目標性能に応じてCu、Mo、Ni、Cr等の合金
元素単体或はこれらの鉄合金を添加することは極
めて有効であり、通常は5%以下の範囲で添加さ
れる。
本発明で使用する被覆剤の成分組成は上記の通
りであるが、この被覆剤を軟鋼心線外周に塗布し
焼成して得られる被覆アーク溶接棒の性能は、被
覆の耐脱落性と密接な関係を有している。即ち先
に説明した如く被覆は溶接時に保護筒を構成し、
アークを安定にすると共にシールド効果を高める
作用があるが、溶接中に被覆が脱落すると上記の
効果が失なわれる。そこで被覆の耐脱落性を改善
すべく研究を行なつたところ、耐脱落性は焼成後
の被覆の嵩密度と密接な関係があり、嵩密度が
2.1g/cm3以上となる様に被覆剤原料の粒度や製
造条件を設定すれば、優れた耐脱落性を確保し得
ることが分つた。ちなみに第1図は、上記成分組
成を満足するイルミナイト系被覆アーク溶接棒に
おける、被覆の嵩密度と溶接中の被覆の脱落回数
及びビード幅の関係を示したグラフである。但し
この実験では4.0mm〓×450mmlの供試棒を使用
し、平板上に240A(A.C.)で下向きコンタクト
溶接を行なつた。また被覆の嵩密度は次式により
算出した。
式中K:嵩密度(g/cm3)
G:溶接棒の両端を切断・除去した後の棒
の重量(g)
l:溶接棒の両端を切断・除去した後の棒
長(cm)
d:心線直径(cm)
D:被覆径(cm)
第1図からも明らかな様に、嵩密度が2.0g/
cm3以下のものは被覆の脱落が著しいのに対し、嵩
密度を2.1g/cm3以上にすると脱落は皆無にな
る。尚直径が4.0mm程度の被覆アーク溶接棒を用
いるときの適正電流は通常140〜180A程度である
から、第1図の実験データ(電流:240A)から
も明らかな様に、本発明の溶接棒は高溶接電流の
条件においても高い耐脱落性を発揮することが理
解される。但し嵩密度が3.1g/cm3を越えるとア
ークの広がりが減少してビード幅が狭くなり、ア
ンダーカツト等の継手欠陥が発生し易くなる。
尚上記嵩密度の好適範囲は、先に説明した好適
成分組成の被覆剤を使用した場合に限つて適合す
るのであつて、異なる成分組成の被覆剤に対して
は同様に考えることはできない。その理由は、被
覆剤中の熱分解成分の種類や配合率等が耐脱落性
に影響を及ぼしている為と考えられる。
被覆の嵩密度を調整する方法は特に限定されな
いが、最も一般的な方法としては、被覆剤原料
の粒度構成を調整する方法。軟鋼心線外周へ塗
布する際の圧力を調整する方法、上記,を
組み合わせた方法、等が挙げられる。
本発明は以上の様に構成されており、被覆剤の
成分組成を特定すると共に、特に焼成後における
被覆の嵩密度を特定範囲に調整することによつ
て、被覆の耐脱落性を著しく高め得ることになつ
た。その結果高電流を適用した高速溶接が可能に
なると共に、被覆の脱落に起因するシールド不足
も解消され、溶接能率及び継手性能向上の2大要
求を一挙に達成し得ることになつた。
次に実験例を挙げて本発明の構成及び作用効果
を明確にする。
実験例 1
第1表に示す成分組成のライム・チテニア系被
覆剤(粒度構成は第2表の通り)を、軟鋼心線
(4mm〓×450mml)外周に塗装圧80Kg/cm2、速度
330m/分で塗布し、130℃で1時間焼成してアー
ク溶接棒を製造した。得られた各溶接棒を使用
し、試験板(材質:SM−41、断面形状:第2
図)上に下向き姿勢で肉盛り溶接(溶接電流:
240A)し、溶接時における被覆の脱落回数、溶
接作業性及び得られた溶接金属のX線性能を調べ
た。結果を第1表に一括して示す。
The present invention relates to a coated arc welding rod, and more particularly to a coated arc welding rod in which the function of the coating as a protective tube is improved, and welding workability and joint performance are enhanced. Various welding methods and welding materials have been proposed to improve welding efficiency and joint performance. However, there are few methods that satisfy both the shortening of the total welding time including post-weld modifications (repair welding) and the joint performance. Particularly when welding using coated arc welding rods such as lime titania or illuminite, high current welding to shorten the welding time will cause the coating to burn and become brittle, resulting in parts of the protective tube being damaged during welding. may fall off. As a result, the function of the covering as a protective tube deteriorates, resulting in insufficient shielding, etc., which not only causes joint defects such as blowholes, but also deteriorates workability. As a result, repair welding becomes necessary, and welding time cannot be shortened. The present inventors focused on the above-mentioned circumstances, and in order to develop a coated arc welding rod that provides excellent welding workability without impairing joint performance, the inventors investigated the composition of the coating material, the physical properties of the coating, etc. We have been conducting research on this. The present invention was completed as a result of such research, and its composition consists of 1 of CaCO 3 and MgCO 3
Species or 2 types: 7 to 25% (weight%: same below),
In a coated arc welding rod in which a lime-titania-based or illuminite-based coating material containing 13 to 40% of TiO 2 and 14 to 33% of SiO 2 is applied to the outer periphery of a mild steel core wire and fired, the coating material after firing is The bulk density of is 2.1~3.1
The gist lies in that it is a coated arc welding rod with excellent resistance to shedding of the coating during welding, which is characterized by a resistance to shedding of the coating during welding. In the present invention, by specifying the composition of the coating material and setting the bulk density of the coating within a specific range after firing, the coating is prevented from falling off during welding, and the original function as a protective tube is maintained. I was able to force it. As a result, high-quality welded joints that do not require repair welding can be obtained with good workability. The basis for setting the numerical range in the present invention will be explained below. CaCO 3 and/or MgCO 3 : 7-25% An essential component as a gas generating agent, and the generated gas protects the weld metal from the atmosphere. 7
If it is less than 25%, shielding will be insufficient and joint defects such as blowholes will easily occur, while if it exceeds 25%, the slag viscosity will decrease and the bead shape will deteriorate. Considering these effects, both substances have the same effect, so one may be used alone or in appropriate amounts in combination. Usually lime, dolomite,
It is added as magnesite etc. In addition, other carbonates such as MnCO 3 and FeCO 3 do not have a sufficient shielding effect because their decomposition temperatures are low. However, a small amount
There is no problem in using it in combination with CaCO 3 or MgCO 3 . TiO2 : 13 to 40% This is an essential component to give the slag a suitable encapsulation property.If it is less than 13%, the slag encapsulation property deteriorates and the beads become convex. However, if it exceeds 40%, the slag releasability deteriorates significantly, and workability, especially in multilayer welding, becomes extremely poor. Rutile, illuminite, etc. are used as raw materials. SiO 2 : 14-33% is an important component as a slag viscosity modifier,
If it is less than 14%, the slag encapsulation becomes unstable due to insufficient viscosity, and the bead shape also deteriorates. Also
If it exceeds 33%, the slag becomes glassy and difficult to peel off. The raw materials used are silica sand, talc, mica and other silicates, including SiO 2 in water glass, which is used as a binder. In the present invention, the above three components are essential components of the coating material, but the following components may be added as necessary. Iron oxide: 3 to 20% in terms of FeO Iron oxide has the effect of improving dissolution into the base metal, and especially in the case of illuminite welding rods, it is necessary to add 3% or more. However, if it is too large, the arc force becomes too strong and undercuts tend to occur, so it must be kept at 20% or less. Illuminite, iron sand, scale, etc. are used as raw materials. Iron powder: 40% or less Increases the amount of deposited metal and increases welding efficiency. However, if it exceeds 40%, the insulation properties of the coating become poor and the bead shape becomes convex, which is not preferable. Note that iron in ferroalloys such as Fe-Mn and Fe-Cr also has the same effect. Alloy powder: 5% or less In order to improve the mechanical properties and corrosion resistance of weld metal, it is extremely difficult to add alloying elements such as Cu, Mo, Ni, Cr, etc. or their iron alloys depending on the target performance. It is effective and is usually added in an amount of 5% or less. The composition of the coating used in the present invention is as described above, but the performance of the coated arc welding rod obtained by applying this coating to the outer periphery of the mild steel core wire and firing it is closely related to the shedding resistance of the coating. have a relationship. That is, as explained earlier, the coating constitutes a protective tube during welding,
It has the effect of stabilizing the arc and increasing the shielding effect, but if the coating falls off during welding, the above effects will be lost. Therefore, we conducted research to improve the shedding resistance of the coating, and found that the shedding resistance is closely related to the bulk density of the coating after firing, and that the bulk density
It has been found that excellent shedding resistance can be ensured by setting the particle size and manufacturing conditions of the coating material raw material so that the particle size is 2.1 g/cm 3 or more. Incidentally, FIG. 1 is a graph showing the relationship between the bulk density of the coating, the number of times the coating falls off during welding, and the bead width in an illuminite-based coated arc welding rod that satisfies the above-mentioned composition. However, in this experiment, a 4.0 mm × 450 mm L test rod was used, and downward contact welding was performed on a flat plate at 240 A (AC). The bulk density of the coating was calculated using the following formula. In the formula, K: Bulk density (g/cm 3 ) G: Weight of the welding rod after cutting and removing both ends (g) l: Rod length after cutting and removing both ends of the welding rod (cm) d : Core wire diameter (cm) D: Coating diameter (cm) As is clear from Figure 1, the bulk density is 2.0g/
If the bulk density is less than 2.1 g/cm 3 , the coating will come off significantly, but if the bulk density is 2.1 g/cm 3 or more, there will be no shedding. Note that when using a coated arc welding rod with a diameter of about 4.0 mm, the appropriate current is usually about 140 to 180 A, so as is clear from the experimental data (current: 240 A) in Figure 1, the welding rod of the present invention It is understood that the material exhibits high resistance to falling off even under conditions of high welding current. However, if the bulk density exceeds 3.1 g/cm 3 , the spread of the arc decreases, the bead width becomes narrow, and joint defects such as undercuts are more likely to occur. It should be noted that the above preferred range of bulk density is applicable only when a coating material having the preferred component composition described above is used, and cannot be similarly considered for coating materials having different component compositions. The reason for this is thought to be that the type and blending ratio of the thermally decomposed components in the coating material have an effect on the shedding resistance. The method of adjusting the bulk density of the coating is not particularly limited, but the most common method is a method of adjusting the particle size structure of the coating material raw material. Examples include a method of adjusting the pressure when applying to the outer periphery of the mild steel core wire, a method that combines the above methods, and the like. The present invention is configured as described above, and by specifying the component composition of the coating material and adjusting the bulk density of the coating within a specific range, especially after firing, it is possible to significantly improve the shedding resistance of the coating. It became a matter of fact. As a result, high-speed welding using high current is possible, and the lack of shielding caused by shedding of the coating has been resolved, making it possible to achieve the two major requirements of welding efficiency and joint performance all at once. Next, experimental examples will be given to clarify the structure and effects of the present invention. Experimental example 1 A lime titenia-based coating agent having the composition shown in Table 1 (particle size composition is shown in Table 2) was applied to the outer periphery of a mild steel core wire (4 mm × 450 mm l ) at a pressure of 80 Kg/cm 2 and a speed of 80 Kg/cm 2 .
It was coated at 330 m/min and fired at 130°C for 1 hour to produce an arc welding rod. Using each of the obtained welding rods, test plates (material: SM-41, cross-sectional shape: 2nd
Figure) Overlay welding in a downward position (welding current:
240A), and the number of shedding of the coating during welding, welding workability, and X-ray performance of the obtained weld metal were investigated. The results are summarized in Table 1.
【表】【table】
【表】
第1表より次の様に考察できる。
(1) 従来棒は被覆の嵩密度が小さい為に溶接中の
脱落回数が多く、溶接作業性が悪いと共に溶接
金属のX線性能も劣悪である。またTiO2が多
過ぎる為にスラグの剥離も劣る。
(2) B−1及び2は炭酸塩の配合率が規定範囲を
外れる比較例で、不足の場合(B−1)はシー
ルド不良により良好なX線性能が得られず、多
すぎると(B−2)、スラグの粘性が低下して
スラグが先行し融合不良を起こす。
(3) B−3及び4はTiO2の配合率が規定範囲を
外れる比較例で、不足の場合(B−3)はスラ
グの被包性が乏しくなつてビード形状が凸状に
なる。一方多すぎると(B−4)スラグの剥離
性が悪く作業性が低下する。
(4) B−5及び6はSiO2の配合率が規定範囲を
外れる比較例で、不足の場合(B−5)はスラ
グの粘性が低下してスラグが先行し融合不良を
起こす。また多すぎると(B−6)、スラグの
剥離性が悪くなる。
(5) B−7及び8は被覆の嵩密度が規定範囲を外
れる比較例で、低すぎると(B−7)被覆の耐
脱落性及びX線性能を満足できず、一方高すぎ
ると(B−8)アークの広がりが小さくなつて
溶接しにくい。
(6) これらに対し本発明の要件を満たす実施例A
−1〜6は、被覆の脱落がなく作業性も良好で
あり、溶接金属のX線性能も優れている。
実験例 2
第3表に示す成分組成のイルミナイト系被覆剤
(粒度構成は第4表の通り)を、軟鋼心線(4.0mm
〓×450mml)外周に実験例1と同じ条件で塗布
し、130℃で1時間焼成して被覆アーク溶接棒を
製造した。得られた各溶接棒を使用し、試験板
(材質:SM−41、断面形状:第3図)上に下向き
姿勢で多層盛り溶接(溶接電流:240A)を行な
い溶接時における被覆の脱落回数、溶接作業性及
び得られた溶接金属のX線性能を調べた。結果を
第3表に一括して示す。[Table] From Table 1, the following conclusions can be drawn. (1) Because the bulk density of the coating on conventional rods is low, they often fall off during welding, resulting in poor welding workability and poor X-ray performance of the weld metal. Also, because there is too much TiO 2 , slag peeling is also poor. (2) B-1 and 2 are comparative examples in which the blending ratio of carbonate is outside the specified range; in the case of insufficient carbonate (B-1), good X-ray performance cannot be obtained due to poor shielding; -2) The viscosity of the slag decreases, leading to the slag leading to poor fusion. (3) B-3 and B-4 are comparative examples in which the TiO 2 blending ratio is outside the specified range, and in the case of insufficient TiO 2 (B-3), the encapsulation of the slag becomes poor and the bead shape becomes convex. On the other hand, if it is too large (B-4), the slag peelability will be poor and workability will be reduced. (4) B-5 and 6 are comparative examples in which the blending ratio of SiO 2 is outside the specified range, and when it is insufficient (B-5), the viscosity of the slag decreases, leading to slag leading to poor fusion. On the other hand, if the amount is too large (B-6), the slag releasability becomes poor. (5) B-7 and 8 are comparative examples in which the bulk density of the coating is outside the specified range; if it is too low (B-7), the shedding resistance and X-ray performance of the coating cannot be satisfied; on the other hand, if it is too high, (B-7) -8) It is difficult to weld because the spread of the arc is small. (6) Example A that satisfies the requirements of the present invention for these
-1 to 6, the coating did not fall off, the workability was good, and the X-ray performance of the weld metal was also excellent. Experimental Example 2 An illuminite coating material having the composition shown in Table 3 (particle size composition is shown in Table 4) was applied to a mild steel core wire (4.0 mm
〓×450mm l ) was coated on the outer periphery under the same conditions as in Experimental Example 1, and baked at 130°C for 1 hour to produce a coated arc welding rod. Using each of the obtained welding rods, multilayer welding (welding current: 240A) was performed on a test plate (material: SM-41, cross-sectional shape: Fig. 3) in a downward position, and the number of times the coating fell off during welding was determined. Welding workability and X-ray performance of the obtained weld metal were investigated. The results are summarized in Table 3.
【表】【table】
【表】
第3表からも明らかな様に、従来のイルミナイ
ト系溶接棒は被覆の脱落が著しく溶接作業性及び
溶着金属のX線性能も劣悪である。また本発明の
要件を1つでも欠くと(比較例D−1〜7)、被
覆の耐脱落性、溶接作業性及びX線性能の何れか
が悪くなり、目的を達成できない。これに対し本
発明の要件を満たす溶接棒(C−1〜6)は、上
記3つの要求性能のすべてにおいて良好な結果を
示している。[Table] As is clear from Table 3, conventional illuminite welding rods suffer from significant shedding of the coating and have poor welding workability and poor X-ray performance of the deposited metal. Moreover, if even one of the requirements of the present invention is lacking (Comparative Examples D-1 to D-7), any one of the shedding resistance of the coating, the welding workability, and the X-ray performance will deteriorate, making it impossible to achieve the objective. On the other hand, the welding rods (C-1 to C-6) that meet the requirements of the present invention show good results in all of the above three required performances.
第1図は、被覆の嵩密度と脱落回数の関係を示
すグラフ、第2,3図は実験例で採用した試験板
の断面形状を示す図である。
FIG. 1 is a graph showing the relationship between the bulk density of the coating and the number of times it falls off, and FIGS. 2 and 3 are diagrams showing the cross-sectional shape of the test plate employed in the experimental example.
Claims (1)
重量%、TiO2:13〜40重量%及びSiO2:14〜33
重量%を含有するライムチタニア系又はイルミナ
イト系の被覆剤を軟鋼心線外周に塗布し焼成した
被覆アーク溶接棒において、焼成後の被覆剤の嵩
密度が2.1〜3.1g/cm3であることを特徴とする溶
接中の被覆の耐脱落性の優れた被覆アーク溶接
棒。1 One or two of CaCO 3 and MgCO 3 : 7 to 25
wt%, TiO2 : 13-40 wt% and SiO2 : 14-33
In a coated arc welding rod in which a lime titania-based or illuminite-based coating containing % by weight is applied to the outer periphery of a mild steel core wire and fired, the bulk density of the coating after firing is 2.1 to 3.1 g/ cm3 . A coated arc welding rod with excellent coating fall-off resistance during welding.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15100780A JPS5772792A (en) | 1980-10-27 | 1980-10-27 | Coated electrode |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15100780A JPS5772792A (en) | 1980-10-27 | 1980-10-27 | Coated electrode |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5772792A JPS5772792A (en) | 1982-05-07 |
| JPS6129836B2 true JPS6129836B2 (en) | 1986-07-09 |
Family
ID=15509244
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15100780A Granted JPS5772792A (en) | 1980-10-27 | 1980-10-27 | Coated electrode |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5772792A (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100415984B1 (en) * | 2001-04-18 | 2004-01-24 | 한국과학기술연구원 | Preparing Method of Iron Thermit Welding Material with Mill Scale |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS5146535A (en) * | 1974-10-18 | 1976-04-21 | Sumikin Welding Electrode Co | |
| US4013987A (en) * | 1975-08-22 | 1977-03-22 | Westinghouse Electric Corporation | Mica tape binder |
| JPS5332847A (en) * | 1976-09-08 | 1978-03-28 | Nikko Yozai Kogyo Kk | Covered electrodes |
-
1980
- 1980-10-27 JP JP15100780A patent/JPS5772792A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5772792A (en) | 1982-05-07 |
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