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JPS6057955B2 - coated arc welding rod - Google Patents
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JPS6057955B2 - coated arc welding rod - Google Patents

coated arc welding rod

Info

Publication number
JPS6057955B2
JPS6057955B2 JP14475378A JP14475378A JPS6057955B2 JP S6057955 B2 JPS6057955 B2 JP S6057955B2 JP 14475378 A JP14475378 A JP 14475378A JP 14475378 A JP14475378 A JP 14475378A JP S6057955 B2 JPS6057955 B2 JP S6057955B2
Authority
JP
Japan
Prior art keywords
weight
welding
illuminite
rutile
particle size
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
JP14475378A
Other languages
Japanese (ja)
Other versions
JPS5570495A (en
Inventor
邦秋 林
英児 三木
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 JP14475378A priority Critical patent/JPS6057955B2/en
Publication of JPS5570495A publication Critical patent/JPS5570495A/en
Publication of JPS6057955B2 publication Critical patent/JPS6057955B2/en
Expired legal-status Critical Current

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  • Nonmetallic Welding Materials (AREA)

Description

【発明の詳細な説明】 本発明は被覆アーク溶接棒に関し、詳細には、比較的安
価な材料費で構成されながら優れた性能を発揮し得る新
規な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 coated arc welding rod, and more particularly to a novel coated arc welding rod that is constructed with relatively low material cost and can exhibit excellent performance.

被覆アーク溶接棒用被覆剤に配合される必須成分の1つ
としてはTiO。
One of the essential components added to the coating material for coated arc welding rods is TiO.

があり、これはスラグ形成剤、スラグの粘度調節剤、ア
ーク安定剤等としての多くの機能を有しており、溶接作
業性、ヒートの美麗化、アンダーカット等継手欠陥の防
止等を確保するうえで極めて重要な役割を果している。
チタニア源としては現在ルチールとイルミナイトが知ら
れている。
It has many functions as a slag forming agent, slag viscosity regulator, arc stabilizer, etc., and ensures welding workability, beautiful heat, and prevention of joint defects such as undercuts. It plays an extremely important role.
Rutile and illuminite are currently known sources of titania.

このうちルチール中のTiO2含有率は極めて高いが、
イルミナイトはTiO2含有率においてルチールよりも
数段劣つており、ルチールに対する補助原料とはなり得
てもルチールの代替物としては不足である。従つてルチ
ールは現在のところ被覆アーク溶接棒用被覆剤のTiO
2原料として不可欠のものとされている。ところで最近
の著しい溶接技術の進歩の中でも被覆アーク溶接棒の需
要比率は依然として溶接材料中最大てあり、ルチールの
消費量も依然として増大傾向にある。しかしルチールは
もはや枯渇状態にあり、その入手は年毎に困難になつて
きた。従つたルチールに代替し得るTiO。材料源の開
拓が強く望まれている。本発明者等は前述の様な事情に
着目し、かねてよりルチールに代わるTiO。
Among these, the TiO2 content in rutile is extremely high,
Illuminite is several steps inferior to rutile in TiO2 content, and although it can be used as an auxiliary raw material for rutile, it is insufficient as a substitute for rutile. Therefore, rutile is currently used as a coating material for coated arc welding rods such as TiO.
It is considered indispensable as a second raw material. However, despite recent remarkable advances in welding technology, the demand for coated arc welding rods remains the highest among all welding materials, and the consumption of rutile is still on the rise. However, rutile is now in a state of depletion, and its acquisition is becoming more difficult every year. TiO can be substituted for rutile according to the following. There is a strong desire to develop material sources. The present inventors have focused on the above-mentioned circumstances and have been developing TiO as a substitute for rutile.

材料を開拓すべく種々研究を進めてきた。その結果Ti
0。を75〜93.5重量%含有する高チタニア鉱物例
えばリユーコクシン(レucoxine)を適度に粒度
調整し、こ・れを被覆剤中に適量配合すると、ルチール
配合の被覆アーク溶接棒に優るとも劣らない性能が確保
できることを知り、舷に本発明を完成するに至つた。即
ち本発明に係る被覆アーク溶接棒はTIO−源・として
TiO2の含有率が75〜93.5重量%で、且つ粒度
が250〜105μのものを80〜95重量%含む粒度
構成の高チタニア鉱物を、全被覆剤中に10〜M重量%
配合してなることを第1の特徴とし、TiO2源として
イルミナナイトおよびTiO2の含有率が75〜93.
5重量%で、且つ粒度が250〜105μのものを80
〜9濾量%含む粒度構成の高チタニア鉱物とを含有し、
全被覆剤中にイルミナイトを10〜詔重量%、高チタニ
ア鉱物を5〜44重量%含有してなることを第2の特徴
とする。
We have been conducting various research to develop new materials. As a result, Ti
0. If a high titania mineral containing 75 to 93.5% by weight, such as leucoxin, is adjusted to an appropriate particle size and incorporated into the coating material in an appropriate amount, it will be as good as a rutile-containing coated arc welding rod. Knowing that the performance could be ensured, the present invention was finally completed. That is, the coated arc welding rod according to the present invention uses a high titania mineral having a particle size structure containing 75 to 93.5% by weight of TiO2 as a TIO source and 80 to 95% by weight of particles with a particle size of 250 to 105μ. from 10 to M% by weight in the total coating material.
The first feature is that the content of illuminite and TiO2 as a TiO2 source is 75 to 93.
5% by weight and a particle size of 250 to 105μ.
Contains a high titania mineral with a particle size structure containing ~9% filtration,
The second feature is that the total coating material contains 10 to 44% by weight of illuminite and 5 to 44% by weight of high titania mineral.

そして得られる被覆アーク溶接棒は市販溶接棒よりも優
れたアーク安定性を示し、溶滴の移行状態もスプレー状
となつて母材とのなじみも優れている。
The resulting coated arc welding rod exhibits better arc stability than commercially available welding rods, has a spray-like droplet transfer state, and has excellent compatibility with the base metal.

しかも本明細書で言う高チタニア鉱物とは、たとえばリ
ユーコクシンの如くこれまで溶接棒用被覆剤の原料とし
ては使用されていないもので、ルチールよりもはるかに
安価に入手でき、前記溶接棒を安価に提供し得ることに
なつた。ところで本発明で使用する高チタニア鉱物とは
、TlO2含有率が75〜93.5重量%のものをいう
。しかしてTiO2含有率が75重量%未満の鉱物では
、TiO2量が少なすぎるためイルミナイトと同様ルチ
ール代替物としての機能が期待できず、一方93.5重
量を越えるTiO2含有率の鉱物は、もはやルチールの
類に属し高価になるから、何れも本発明の目的には合致
しない。またこの高チタニア鉱物は、その使用に当り粒
度250〜105μのものの含有率が80〜95重量%
となる様に粒度調整しなければならない。その理由は後
記実施例で詳細に説明するが、粒度構成が粗目になると
、アークがj烈しくなるほか母材とのなじみも悪くなつ
て溶接作業性及び継手性能が劣化し、一方細目になりす
ぎると、アークカが弱くなつてクレータの拡がりが小さ
くなるなど溶接作業性が低下するからである。尚ルチー
ル、イルミナイト及び本発明で言う高チタニア鉱物の代
表例であるリユーコクシンの化学成分の一例を第1表に
示す。
Furthermore, the high titania minerals referred to in this specification are minerals such as lyucoccin, which have not been used as raw materials for coating materials for welding rods, and can be obtained much more cheaply than rutile, making it possible to make the welding rods cheaper. Now we can provide it. By the way, the high titania mineral used in the present invention refers to one having a TlO2 content of 75 to 93.5% by weight. However, minerals with a TiO2 content of less than 75% by weight cannot be expected to function as a rutile substitute like illuminite because the amount of TiO2 is too small, while minerals with a TiO2 content of more than 93.5% by weight can no longer be Since they belong to the rutile family and are expensive, none of them meet the purpose of the present invention. In addition, when using this high titania mineral, the content of particles with a particle size of 250 to 105μ is 80 to 95% by weight.
The particle size must be adjusted so that The reason for this will be explained in detail in the examples below, but when the grain size structure becomes coarse, the arc becomes more intense and the compatibility with the base metal deteriorates, resulting in poor welding workability and joint performance, while on the other hand, when the grain size becomes too fine, This is because the arc force becomes weaker and the spread of the crater becomes smaller, resulting in a decrease in welding workability. Table 1 shows an example of the chemical components of rutile, illuminite, and leucoccin, which is a representative example of the high titania mineral referred to in the present invention.

次に上記TlO2含有率及び粒度構成を共に満足する高
チタニア鉱物の配合率であるが、これは全被覆剤に対し
て10〜54重量%の範囲に設定しなければならない。
Next is the blending ratio of the high titania mineral that satisfies both the TlO2 content and particle size structure, which must be set in the range of 10 to 54% by weight based on the total coating material.

しかして高チタニア鉱物の配合率が少なすぎると、アー
クの安定性、溶滴移行状態及びクレータの拡がりが悪化
するほか母材とのなじみが悪くなつて当初の目的が達成
できず、一方配合率が54重量%を越えると、スラグの
流動性が過大になつてスラグ浴が極めて不安定になるほ
か、スラグの剥離性が著しく悪化する。この場.合、被
覆剤中には高チタニア鉱物のほか炭酸塩鉱物を16〜4
唾量%及びカリ長石を9〜3哩量%含有させることが望
まれる。その理由は、炭酸塩鉱物が多すぎてもまた少な
すぎても、アークカの強さ、アークの安定性、溶滴移行
状態、クレータの−拡がり、母材とのなじめ等が概して
悪くなる傾向があり、またカリ長石が前記好適範囲を外
れると前記諸性能のすべてが極端に低下するからである
。次にTiO2源として上記高チタニア鉱物以外にイル
ミナイトが含まれているときは、高チタニア鉱物の配合
率を5〜44重量%を設定することができる。
However, if the blending ratio of high titania minerals is too low, the stability of the arc, the droplet transfer state, the spread of the crater will deteriorate, and the compatibility with the base material will become poor, making it impossible to achieve the original purpose. If the amount exceeds 54% by weight, the fluidity of the slag becomes excessive, making the slag bath extremely unstable, and the peelability of the slag deteriorates significantly. This place. In addition to high titania minerals, carbonate minerals are also included in the coating.
It is desirable to contain 9% to 3% of saliva and potassium feldspar. The reason for this is that, whether there is too much or too little carbonate mineral, arc strength, arc stability, droplet transfer conditions, crater spread, and compatibility with the base metal generally tend to deteriorate. Moreover, if the potassium feldspar is out of the above-mentioned preferred range, all of the above-mentioned performances will be extremely degraded. Next, when illuminite is included as a TiO2 source in addition to the above-mentioned high titania mineral, the blending ratio of the high titania mineral can be set to 5 to 44% by weight.

即ち被覆剤中にイルミナイトが含まれていると、これが
TiO2の補助原料となつてTiO2の総含有率が高く
なるから、高チタニア鉱物の配合率を若干少ないめに抑
えるべきである。この場合、被覆剤中には高チタニア鉱
物のほかイルミナイトを10〜35重量%含有させなけ
ればならない。その理由は、イルミナイトが1鍾量%未
満ではアーク力が弱くなつて安定性が低下するほか、溶
滴移行状態、クレータの拡がり、母材とのなじみが悪化
しスラグの流動性が過大になる傾向があるからである。
また、炭酸塩鉱物(石灰石、ドロマイト等)を5〜2唾
量%含有させることが望まれ、炭酸塩鉱物の含有率が5
重量%未満或は2踵量%超の何れでも、アークカの強さ
、アーク安定性、溶滴移行状態、クレータの拡がり等す
べての性能が低くなる傾向がある。本発明は概略以上の
様に構成されるが、要は所定範囲のTlO2含有率を有
し所定の粒度構成に粒度調整した高チタニア鉱物を、被
覆剤中に所定量配合したことを第1の特徴とし、前記高
チタニア鉱物とイルミナイトとをそれぞれ被覆剤中に所
定量配合したことを第2の特徴とし、殊にルチールの代
替鉱物として比較的安価に入手てきるリユーコクシン等
を使用することにより、安価で高性能の被覆アーク溶接
棒が得られることになつた。
That is, if illuminite is contained in the coating material, it will serve as an auxiliary material for TiO2 and the total content of TiO2 will increase, so the blending ratio of high titania minerals should be kept to a slightly lower level. In this case, the coating must contain 10 to 35% by weight of illuminite in addition to the high titania mineral. The reason for this is that if the amount of illuminite is less than 1%, the arc force becomes weak and stability decreases, and the fluidity of the slag becomes excessive due to the droplet transfer state, the spread of craters, and poor compatibility with the base material. This is because there is a tendency to
In addition, it is desirable to contain carbonate minerals (limestone, dolomite, etc.) by 5 to 2%, and the content of carbonate minerals is 5% to 2%.
If the amount is less than 2% by weight or more than 2% by weight, all performances such as arc strength, arc stability, droplet transfer state, and crater spread tend to deteriorate. The present invention is generally constructed as described above, but the key point is that the first step is to blend a predetermined amount of high titania mineral having a TlO2 content within a predetermined range and whose particle size is adjusted to a predetermined particle size composition into a coating material. The second feature is that the high titania mineral and illuminite are each blended in predetermined amounts in the coating material, and in particular, by using lyucoccine, etc., which can be obtained relatively cheaply as a substitute mineral for rutile. As a result, an inexpensive and high-performance coated arc welding rod can be obtained.

従つて本発明では原則としてルチールを使用しない点に
特徴があるが、ルチール自体は性能面では何ら障害とな
ることはないので、少量のルチールを併用することを積
極的に排除するものではない。このほか本発明では前記
成分以外に珪砂、マイカ、タルク等の珪酸塩、砂鉄、二
酸化マンガン、アルミナ等の酸化物、螢石や氷晶石等の
弗化物、Fe−Si..Fe−Mn等の成分調整剤、鉄
粉、澱粉、アルギン酸ソーダ等の有機物や水ガラス等の
粘結*8剤等が必要に応じて適量配合されるが、高チタ
ニア鉱物のTlO2含有率、粒度構成及び被覆剤中への
配合率が前記の要件を満たす限りすべて本発明技術の範
鴫に含まれる。次に実験例を挙げて本発明を説明するが
、下記は本発明を限定する主旨ではなく、前・後記の趣
旨に沿つて適当に変更して実施することも勿論本発明範
囲内の実施とみるべきである。
Therefore, the present invention is characterized in that rutile is not used in principle, but since rutile itself does not pose any problem in terms of performance, the concomitant use of a small amount of rutile is not positively excluded. In addition to the above-mentioned components, the present invention uses silica sand, silicates such as mica and talc, oxides such as iron sand, manganese dioxide and alumina, fluorides such as fluorite and cryolite, Fe-Si. .. Component regulators such as Fe-Mn, iron powder, starch, organic substances such as sodium alginate, and caking agents such as water glass are added in appropriate amounts as necessary, but the TlO2 content and particle size of high titania minerals All of them fall within the scope of the technology of the present invention as long as the composition and blending ratio in the coating material meet the above requirements. Next, the present invention will be explained with reference to experimental examples, but the following is not intended to limit the present invention, and it is of course possible to implement the present invention with appropriate modifications in accordance with the spirit of the preceding and following. You should see it.

実験例1 イルミナイト、砂鉄、鉄鉱石等が配合される被覆系の一
例としてイルミナイト系を選択し、高チタニア鉱物とし
てリユーコクシンを用いた場合の実験結果を示す。
Experimental Example 1 Experimental results will be shown in which an illuminite system is selected as an example of a coating system in which illuminite, iron sand, iron ore, etc. are blended, and leucoccin is used as a high titania mineral.

使用したリユーコクシンの化学成分を第2表、粒度構成
を第3表、供試批覆剤の基本配合を第4表、、該基本配
合の一部を構成する副配合αを第5表に夫々示す。
The chemical components of the ryukoccin used are shown in Table 2, the particle size composition is shown in Table 3, the basic formulation of the test reversal agent is shown in Table 4, and the sub-composition α that constitutes a part of the basic formulation is shown in Table 5. .

まず第4表に示した基本配合Mを選択し、これに第6表
に示す比率でリユーコクシン(第2,3表)を配合して
得た被覆剤を、直径4.0WR1長さ40077177
!の軟鋼心線に対して被覆剤が6.25顛となる様に塗
布する。
First, the basic formulation M shown in Table 4 was selected, and a coating material obtained by blending ryukoccin (Tables 2 and 3) in the ratio shown in Table 6 was coated with a coating material having a diameter of 4.0 WR and a length of 40077177 mm.
! Coat the coating material to a thickness of 6.25 to the mild steel core wire.

得られた供試溶接棒を用い、溶接一電流145〜170
A(A−C)で且つ全姿勢で溶接したときの作業性を観
察した。尚溶接作業性は次の項目毎に判定した。
Using the obtained test welding rod, welding current 145 to 170
Workability was observed when welding was performed in A (A-C) and in all positions. The welding workability was evaluated based on the following items.

(1)アークの強さ :強い方がよい(2)アーク
の安定性 :安定な方がよい(3)溶滴移行状態
:スプレー状の方がよい(4)クレータの拡がり :
大きい方がよい(5)母材とのなじみ :なじみ易い
方がよい(6)スラグの邪魔 :邪摩しない方がよ
い(7)スラグの剥離性 :剥離し易い方がよい結果
を第7表に示す。
(1) Arc strength: The stronger the better (2) Arc stability: The more stable the better (3) Droplet transfer state
: Spray form is better (4) Crater spread:
The larger the size, the better (5) Compatibility with the base material: The easier it is to fit in, the better (6) Obstruction of the slag: It is better not to rub it in. (7) Peelability of the slag: The easier it is to peel, the better the results are shown in Table 7 Shown below.

第7表の結果からも明らかな様に、リユーコクシンの配
合率が少なすぎてもまた多すぎても優れた溶接作業性は
得られないが、その配合率が5〜4種量%の範囲におい
ては、何れの場合も市販品を凌駕する溶接作業性が得ら
れる。
As is clear from the results in Table 7, excellent welding workability cannot be obtained if the blending ratio of ryukoccin is too low or too high, but when the blending ratio is in the range of 5 to 4%, In either case, welding workability superior to commercially available products can be obtained.

次に第4表における基本配合M以外のものについて、基
本配合/リユーコクシンを7鍾量%/30重量%に設定
した被覆剤を調整し、前記と同様にして得た各供試溶接
棒の溶接作業性を観察した。
Next, for those other than the basic formulation M in Table 4, a coating material with the basic formulation/Ryucoccin set at 7% by weight/30% by weight was prepared, and each test welding rod obtained in the same manner as above was welded. Workability was observed.

結果を第8表に示す。第8表の結果からも明らかな如く
、リユーコクシンの配合率が好適範囲に入つている場合
(本例では3唾量%)でも、イルミナイト及び石灰石の
含有率の両者が好適範囲に入つていなければ、優れた溶
接作業性は得られ難い。
The results are shown in Table 8. As is clear from the results in Table 8, even when the ryukoccin content is within the preferred range (3% in this example), both the illuminite and limestone content are within the preferred range. Without it, it is difficult to obtain excellent welding workability.

しかしこれらをすべて満足する供試棒番号13,14,
15,18,19,22,23及び24では市販品を凌
駕する溶接作業性が得られている。次に溶接作業性に及
びすリユーコクシンの粒度構成の影響を確認するため、
第9表に示す3種の粒度構成のリユーコクシンを準備し
、これを第4表の基本配合Mでリユーコクシンの配合率
を7重量%及ひ42重量%(何れも本発明の規定範囲内
)にしたときの夫々の溶接作業性を前記と同様にして観
察した。
However, test rod numbers 13 and 14, which satisfy all of these requirements,
Nos. 15, 18, 19, 22, 23, and 24 have welding workability that exceeds that of commercially available products. Next, in order to confirm the influence of the particle size composition of Ryukokushin on welding workability,
Prepare ryukoccin with the three particle size configurations shown in Table 9, and adjust the blending ratio of ryukoccin to 7% by weight and 42% by weight (both within the specified range of the present invention) using the basic formulation M shown in Table 4. The welding workability of each was observed in the same manner as above.

注 イニ本発明範囲内のもの(第2表と同一)ロニ本発
明範囲より粗目のものハニ本発明範囲より細目のもの 結果を第1咳に示す。
Note: Items within the scope of the present invention (same as Table 2) Items that are coarser than the scope of the present invention H: Items that are finer than the scope of the present invention The results are shown in No. 1.

市販品:同前◎,0,Δ,×:同前 第1咳の結果からも明らかな如く、たとえリユーコクシ
ンの配合率が本発明で規定する範囲内であつても、リユ
ーコクシンの粒度構成が規定範囲を外れた場合(供試棒
番号2−0,2−ハ,5ーロ,5−ハ)は、満足な溶接
作業性が得られない。
Commercial product: Same as before ◎, 0, Δ, ×: As is clear from the results of the first cough from the same day, even if the blending ratio of ryukoccin is within the range specified by the present invention, the particle size structure of ryucoccin is not specified. If it is outside the range (sample rod numbers 2-0, 2-c, 5-ro, 5-c), satisfactory welding workability cannot be obtained.

しかし粒度構成が規定範囲内のリユーコクシンを使用す
ると(供試棒番号2−イ,5−イ)、市販品よりも優れ
た溶接作業性を得ることができる。実験例2 イルミナイト、砂鉄、鉄鉱石等が配合されない被覆系の
一例としてライム、チタニア系を選択し、高チタニア鉱
物としてリユーコクシンを用いた場合の実験結果を示す
However, when using Ryukoxin whose particle size structure is within the specified range (test rod numbers 2-I and 5-I), it is possible to obtain better welding workability than commercially available products. Experimental Example 2 Experimental results are shown in which lime and titania are selected as an example of a coating system in which illuminite, iron sand, iron ore, etc. are not blended, and leucoccin is used as the high titania mineral.

使用したリユーコクシンは実験例1と同一のものである
The ryukoccin used was the same as in Experimental Example 1.

供試被覆剤の基本配合を第11表に、該基本配合の一部
を構成する副配合βを第1渋に夫々示す。第11表に示
した基本配合N″を選択し、これに第1談に示す比率で
リユーコクシン(第1,2表)を配合して得た被覆剤を
、直径4.0wn1長さ400wtの軟鋼心線に対して
被覆径が6.30陽となる様に塗布する。
The basic formulation of the sample coating material is shown in Table 11, and the sub-mixture β forming a part of the basic formulation is shown in Table 1. The basic composition N'' shown in Table 11 was selected, and the coating material obtained by blending Ryucoccin (Tables 1 and 2) in the ratio shown in Part 1 was applied to a mild steel of 4.0wn in diameter and 400wt in length. Apply the coating so that the coating diameter is 6.30 mm on the core wire.

得られた供試溶接棒を用い、溶接電流150〜180A
(A−C)で且つ全姿勢で溶接し7たときの作業性を観
察した。尚溶接作業性の判定要領は実験例1と同様てあ
;る。
Using the obtained test welding rod, welding current 150-180A
(A-C) and when welding in all positions, the workability was observed. The procedure for determining welding workability is the same as in Experimental Example 1.

結果を第14表に示す。The results are shown in Table 14.

市販品:ライム・チタニア系被覆アーク溶接棒◎,0,
Δ,×:同前第14表の結果からも明らかな様に、リユ
ーコクシンが少なすぎてもまた多すぎても優れた溶接作
業性は得られないが、その配合率が10〜鴻量%の範囲
においては、何れの場合も市販品を凌駕する溶接作業性
が得られる。
Commercially available product: Lime titania coated arc welding rod ◎, 0,
Δ, Within this range, welding workability superior to commercially available products can be obtained in any case.

次に第11表における基本配合N″以外のものについて
、基本配合/リユコクシンを7踵量%/23重量%に設
定した被覆剤を調製し、前記と同様に化て得た各供試溶
接棒の溶接作業性を観察した。結果を第1俵に示す。第
1俵の結果からも明らかな如く、リユーコクシンの配合
率が好適範囲に入つている場合(本例では2踵量%)で
も、石灰石及びカリ長石の含有一率の両者が好適範囲に
入つていなければ、優れた溶接作業性は得られ難い。
Next, for those other than the basic formulation N'' in Table 11, a coating material was prepared with the basic formulation/ryukoccin set at 7% by weight/23% by weight, and each test welding rod was obtained in the same manner as above. Welding workability was observed.The results are shown in the first bale.As is clear from the results of the first bale, even when the blending ratio of ryukoccin is within the preferred range (in this example, 2%), Unless both the content percentages of limestone and potassium feldspar are within the preferred range, it is difficult to obtain excellent welding workability.

しかしこれらをすべて満足する供試棒番号43,44,
45,48,49,52,53,54では市販品を凌駕
する溶接作業性が得られる。次にライム●チタニア系の
ものについても、溶接作業性に及ぼすリユーコクシンの
粒度構成の影響を確認するため、実験例1と同様第9表
に示した粒度構成のリユーコクシンを準備し、これを第
11表の基本配合N″でリユーコクシンの配合率を1踵
量%及び5種量%(何れも本発明の規定範囲内)にした
ときの溶接作業性を、実験例1と同様にして観察した。
However, test rod numbers 43, 44, which satisfy all of these requirements,
No. 45, 48, 49, 52, 53, and 54 provide welding workability superior to commercially available products. Next, in order to confirm the influence of the particle size composition of Lieucoccin on the welding workability for lime-titania-based products, we prepared Lieucoccin with the particle size composition shown in Table 9 as in Experimental Example 1, and The welding workability was observed in the same manner as in Experimental Example 1 when the mixing ratio of ryukoccin was 1 heel weight % and 5 seed weight % (both within the specified range of the present invention) in the basic formulation N'' shown in the table.

結果を第1俵に示す。The results are shown in the first bale.

Claims (1)

【特許請求の範囲】 1 TiO_2源として、TiO_2の含有率が75〜
93.5重量%であると共にその80〜95重量%は2
50〜105μの粒度構成からなるものである高チタニ
ア鉱物を被覆剤中に含有し、該高チタニア鉱物を、全被
覆剤中に10〜54重量%含有してなることを特徴とす
る被覆アーク溶接棒。 2 TiO_2源として、イルミナイトおよびTiO_
2の含有率が75〜93.5重量%であると共にその8
0〜95重量%は250〜105μの粒度構成からなる
ものである高チタニア鉱物を被覆剤中に含有し、被覆剤
中にイルミナイトを10〜35重量%、高チタニア鉱物
を5〜44重量%含有してなることを特徴とする被覆ア
ーク溶接棒。
[Claims] 1. As a TiO_2 source, the content rate of TiO_2 is 75 to
93.5% by weight and 80-95% by weight is 2
Coated arc welding, characterized in that the coating material contains a high titania mineral having a grain size of 50 to 105μ, and the high titania mineral is contained in an amount of 10 to 54% by weight in the total coating material. rod. 2 Illuminite and TiO_2 as sources of TiO_2
The content of 2 is 75 to 93.5% by weight, and the 8
0 to 95% by weight consists of a particle size composition of 250 to 105μ High titania minerals are contained in the coating, 10 to 35% by weight of illuminite and 5 to 44% by weight of high titania minerals are contained in the coating. A coated arc welding rod characterized by containing:
JP14475378A 1978-11-21 1978-11-21 coated arc welding rod Expired JPS6057955B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP14475378A JPS6057955B2 (en) 1978-11-21 1978-11-21 coated arc welding rod

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP14475378A JPS6057955B2 (en) 1978-11-21 1978-11-21 coated arc welding rod

Publications (2)

Publication Number Publication Date
JPS5570495A JPS5570495A (en) 1980-05-27
JPS6057955B2 true JPS6057955B2 (en) 1985-12-17

Family

ID=15369570

Family Applications (1)

Application Number Title Priority Date Filing Date
JP14475378A Expired JPS6057955B2 (en) 1978-11-21 1978-11-21 coated arc welding rod

Country Status (1)

Country Link
JP (1) JPS6057955B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS58209498A (en) * 1982-05-06 1983-12-06 Kawasaki Steel Corp Covered electrode
JP5415891B2 (en) * 2009-10-07 2014-02-12 株式会社神戸製鋼所 Titanium oxide raw material for welding materials, flux cored wire, coated arc welding rod and flux for submerged arc welding
RU2630059C2 (en) * 2015-06-30 2017-09-05 Виктор Григорьевич Лозовой Electrode coating composition

Also Published As

Publication number Publication date
JPS5570495A (en) 1980-05-27

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