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JPS5852476B2 - Melt flux for horizontal submerged arc welding - Google Patents
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JPS5852476B2 - Melt flux for horizontal submerged arc welding - Google Patents

Melt flux for horizontal submerged arc welding

Info

Publication number
JPS5852476B2
JPS5852476B2 JP17242779A JP17242779A JPS5852476B2 JP S5852476 B2 JPS5852476 B2 JP S5852476B2 JP 17242779 A JP17242779 A JP 17242779A JP 17242779 A JP17242779 A JP 17242779A JP S5852476 B2 JPS5852476 B2 JP S5852476B2
Authority
JP
Japan
Prior art keywords
slag
flux
bead
arc welding
submerged arc
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
JP17242779A
Other languages
Japanese (ja)
Other versions
JPS5692000A (en
Inventor
芳雄 佐藤
辰美 細野
勲 杉岡
茂雄 木村
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.)
Nippon Steel Corp
Original Assignee
Nippon Steel Corp
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 Nippon Steel Corp filed Critical Nippon Steel Corp
Priority to JP17242779A priority Critical patent/JPS5852476B2/en
Publication of JPS5692000A publication Critical patent/JPS5692000A/en
Publication of JPS5852476B2 publication Critical patent/JPS5852476B2/en
Expired legal-status Critical Current

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Description

【発明の詳細な説明】 本発明は横向潜弧溶接用メルトフラックスtこ関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a melt flux for horizontal submerged arc welding.

横向潜弧溶接法は、軟鋼〜I(T−60鋼あるいは低温
鋼など広い範囲に適用されており、これら(こ使用され
ているフラックスは通常の下向姿勢で用いられるフラッ
クス1こ比べ特別な性能が要求される。
The horizontal submerged arc welding method is applied to a wide range of steels, including mild steel to T-60 steel and low-temperature steel. Performance is required.

すなわち横向潜弧溶接は一般の下向溶接とは異り、溶接
入熱量が小さいため]こ溶接金属および溶融スラグの凝
固が早くビード表面]こアバタやポックマークが発生し
やすく、狭い開先角度が採用されるのでスラグの剥離性
が悪くなる。
In other words, unlike general downward welding, horizontal submerged arc welding has a small welding heat input, so the weld metal and molten slag solidify quickly on the bead surface, which tends to cause flutter and pock marks, and a narrow bevel angle. is adopted, so the slag removability becomes poor.

また溶接金属内部の凝固方向はビード上側では下向き1
こなるので、スラグ巻込みやブロホールがビード内1こ
残留しやすいという問題がある。
Also, the solidification direction inside the weld metal is downward 1 on the upper side of the bead.
As a result, there is a problem in that slag entrainment and blowholes tend to remain in the bead.

すなわち、低入熱でかつ凝固方向が下向1こなる部分を
つくる横向溶接では、ブロホールやスラグ巻込みが発生
しやすく、ビード表面]こもアバタ、ポックマークが発
生する事1こなる。
That is, in lateral welding, which involves low heat input and creates a part where the solidification direction is downward, blowholes and slag entrainment are likely to occur, resulting in the bead surface being sluggish and having pockmarks.

そこで本発明者等はこのような特殊の溶接姿勢で、かつ
小人熱の潜弧溶接を行なっても上記欠陥のない良好な溶
接金属を得るために、メルトフラックス組成について検
討した結果、次の組成域1こおいてこれらを満足するこ
とを見出した。
Therefore, in order to obtain a good weld metal without the above defects even when performing latent arc welding using dwarf heat in such a special welding position, the inventors investigated the melt flux composition and found the following. It has been found that composition range 1 satisfies these requirements.

すなわち本発明はフラックス必須成分が5i0221〜
30%、Mn05〜15%、CaO3〜15□、A12
0321〜30%、CaF220〜30%からなり、上
記必須成分のS 102 + N1203+CaF2−
68〜83%であり、且つMgOを2%未満tこ制限し
、またかさ密度が1.49/i超であることを特徴とす
る横向潜弧溶接用メルトフラックスである。
That is, in the present invention, the essential flux components are 5i0221~
30%, Mn05-15%, CaO3-15□, A12
0321-30%, CaF220-30%, and the above essential components S 102 + N1203 + CaF2-
68 to 83%, limits MgO to less than 2%, and has a bulk density of more than 1.49/i.

即ちCaF2およびAl2O3の他にSiO2,MnO
,CaOを適量添加し、且つスラグの流動性の悪くなる
MgOをできるだけ減少させること1こよって溶接作業
性を小人熱の横向姿勢1こ適するよう向上せしめ、その
結果柱状晶の凝固が下側1こ向って進行していく不自然
な溶接姿勢1こおいても、溶融スラグの浮上を容易Iこ
すると共1こ、ポックマーク、アバク等の発生原因とな
るco 、 co□ガス等の逸出を容易にした。
That is, in addition to CaF2 and Al2O3, SiO2, MnO
, by adding an appropriate amount of CaO and reducing as much as possible MgO, which deteriorates the fluidity of the slag1.Thus, welding workability is improved to suit the horizontal position of the dwarf heat, and as a result, the solidification of columnar crystals is Even in an unnatural welding position in which the welding progresses in the opposite direction, the molten slag easily floats up and scrapes, as well as the escape of CO, CO□ gas, etc., which causes pockmarks, abductions, etc. It made it easier to get out.

またCaF2が高いために溶接金属部の酸素量、水素量
も低くなり、切欠き靭性も良好となり、またMnOを添
加しているのでビード形状をも良好となるものである。
Furthermore, since the CaF2 content is high, the amount of oxygen and hydrogen in the weld metal part is also low, and the notch toughness is also good, and since MnO is added, the bead shape is also good.

以下)こ本発明の詳細な説明する。The present invention will be described in detail below.

先ず各成分側の限定理由を述べると次の通りである。First, the reasons for the limitations on each component are as follows.

S i02は21%未満ではポックマークが発生し易く
なり、また溶接金属の水素量も多くなり好ましくない。
If S i02 is less than 21%, pock marks tend to occur and the amount of hydrogen in the weld metal increases, which is not preferable.

30%を超えるフラックスの融点が上昇するため良好な
スラグの剥離性が得られない。
Since the melting point of flux exceeding 30% increases, good slag releasability cannot be obtained.

従って8102は21〜30%未満ではポックマークが
発生し、またスラグ剥離性が悪くなり好ましくない。
Therefore, if 8102 is less than 21 to 30%, pock marks occur and slag removability becomes poor, which is not preferable.

CaOは15%を超えるとフラックスの融点が上がりス
ラグの流動性が悪くなり、スラグ巻込みが発生しゃすく
ビード外観も悪くなる。
If CaO exceeds 15%, the melting point of the flux will rise, the fluidity of the slag will deteriorate, slag entrainment will occur, and the bead appearance will also deteriorate.

MnOは15%を超えると逆1こ融点が下がりすぎ、ビ
ード外観的1こも悪くなる。
If MnO exceeds 15%, the melting point will drop too much and the appearance of the bead will deteriorate.

従ってMnO,CaOは夫々5〜15%の範囲1こする
必要がある。
Therefore, each of MnO and CaO must be in the range of 5 to 15%.

Al2O3は高CaF2系溶融スラグの耐火性およびス
ラグの剥離性を良好1こするため必要であるが、21%
未満ではその効果がなく、ビードのたれ下りが生じ易く
なり好ましくない。
Al2O3 is necessary to improve the fire resistance of high CaF2-based molten slag and the peelability of the slag, but at 21%
If it is less than that, the effect is not achieved and the bead tends to sag, which is not preferable.

30%を超えると融点が高くなりすぎ、スラグ剥離性、
ビード形状が悪くなり好ましくない。
If it exceeds 30%, the melting point will become too high, and the slag removability will deteriorate.
This is not preferable because the bead shape deteriorates.

従ってA4203は21〜30%の範囲1こする必要が
ある。
Therefore, A4203 needs to be rubbed in the range 21-30%.

CaF2は20%未満ではスラグの流動性が悪く、スラ
グ巻込みやブロホールが発生しやすくなると共1こ、ビ
ード表面にポックマークが発生しやすくなるので好まし
くない。
If CaF2 is less than 20%, the fluidity of the slag is poor and slag entrainment and blowholes are more likely to occur, and pock marks are more likely to occur on the bead surface, which is not preferable.

30%を超えるとスラグの流動性は良好1こなるが、融
点が低下しすぎ、またアークが不安定となり良好なビー
ド形状が得られないのでこれ以下でなければならない。
If it exceeds 30%, the fluidity of the slag will be good, but the melting point will drop too much and the arc will become unstable, making it impossible to obtain a good bead shape, so it must be below this range.

また必須成分のS i02 、Ae 203及びCaF
2の3者合計を68〜83%の範囲としたのは、次のよ
うな実験1こよって得られた知見)こ基くものである。
In addition, the essential components S i02 , Ae 203 and CaF
The reason why the total of the three factors in 2 was set in the range of 68 to 83% was based on the knowledge obtained from the following experiment 1).

即ち必須成分のCa010%、MnOL 1%に固定し
て5i0221〜30%A120321〜30%、Ca
F220〜30%の成分範囲内でSiO2+Al2O3
+CaF2添加量を63〜88%まで変化させたフラッ
クスを用い、その時の溶着金属の拡散性水素量、ポック
マーク、スラグ剥1雅性、ビード形状、アーク安定性t
こついて調べた。
That is, the essential components Ca010%, MnOL fixed at 1%, 5i0221~30%A120321~30%, Ca
SiO2+Al2O3 within the component range of F220-30%
Using flux with +CaF2 addition amount varying from 63 to 88%, the amount of diffusible hydrogen in the weld metal, pockmarks, slag peeling elegance, bead shape, arc stability t
I researched it carefully.

実験方法としては溶着金属の拡散性水素はJISZ31
.13−1951.1こ規定された溶着金属の水素量測
定方法1こ準じて測定した。
As for the experimental method, the diffusible hydrogen of the weld metal is determined according to JIS Z31.
.. The hydrogen content was measured in accordance with the method for measuring the amount of hydrogen in weld metal specified in 13-1951.1.

その時の試験板およびワイヤの化学成分を第1表1こ溶
接条件を第2表に示す。
The chemical composition of the test plate and wire at that time is shown in Table 1, and the welding conditions are shown in Table 2.

またポックマーク、ビード形状、スラグ剥離性、アーク
安定性1こついては第1図に示す開先形状(寸法単位m
vt’)を用い、第4表1こ示した溶接条件と、第2図
1こ示す溶接ビードの積層法(図中の数字は積層順)を
用いた。
In addition, regarding pockmarks, bead shape, slag removability, and arc stability, the groove shape shown in Figure 1 (dimension unit: m)
vt'), the welding conditions shown in Table 4 and the weld bead stacking method shown in FIG. 2 (the numbers in the figure indicate the order of stacking) were used.

その時の試験板およびワイヤの化学成分は第3表1こ示
すが、試験板SP■50Q鋼で板厚25間、巾200叩
、長さ7501mの犬ぎさの板を第1図のよう]こ開先
加工を行ない横向潜弧溶接を行なった。
The chemical composition of the test plate and wire at that time is shown in Table 3. The test plate was made of SP50Q steel with a thickness of 25 mm, width of 200 mm, and length of 7501 m as shown in Figure 1. A groove was prepared and horizontal submerged arc welding was performed.

その結果として5i02+A6203+CaF2の添加
量を拡散性水素量、ポックマーク、スラグ剥離性、ビー
ド形状、アーク安定性との関係を第3図に示す。
As a result, the relationship between the amount of 5i02+A6203+CaF2 added and the amount of diffusible hydrogen, pockmarks, slag removability, bead shape, and arc stability is shown in FIG.

フラックス中のSiO2+Al2O3+CaF2が68
%未満では溶着金属の拡散性水素量が上昇し、またポッ
クマークが発生しやすくなりビード外観が悪くなるので
好ましくない。
SiO2+Al2O3+CaF2 in flux is 68
If it is less than %, the amount of diffusible hydrogen in the weld metal increases, pock marks are likely to occur, and the bead appearance deteriorates, which is not preferable.

一方83%を超えるとスラグ剥離性が悪くなる。On the other hand, if it exceeds 83%, the slag removability deteriorates.

またアークが不安定となり、ビード形状も悪くなるので
、SiO2+Al2O3+CaF2は68〜83%の範
囲1こする必要がある。
Furthermore, the arc becomes unstable and the bead shape deteriorates, so it is necessary to rub SiO2 + Al2O3 + CaF2 in a range of 68 to 83%.

また上記必須成分とは別に、MgO成分を2%未満1こ
制限する必要がある。
In addition to the above-mentioned essential components, it is necessary to limit the MgO component to less than 2%.

MgOはビード外観を良好1こするためFこ2%未満ま
で使用できるが、2%を超えると溶接金属の水素量が増
加しポックマークが発生しやすいので、2%未満1こ抑
えることが必要である。
MgO can be used up to less than 2% to improve the appearance of the bead, but if it exceeds 2%, the amount of hydrogen in the weld metal increases and pock marks are likely to occur, so it is necessary to keep it below 2%. It is.

またかさ密度は1.4g/−超とする必要がある。Moreover, the bulk density needs to be more than 1.4 g/-.

かさ密度が1.4g/−以下になるとスラグ剥離性が悪
くなり、またビード形状が垂れやすくなり、さら1こ溶
接金属の水素量および窒素が増加するので好ましくない
ので、かさ密度は1.4g/−超とする。
If the bulk density is less than 1.4 g/-, the slag removability will be poor, the bead shape will tend to sag, and the amount of hydrogen and nitrogen in the weld metal will increase, which is undesirable. Therefore, the bulk density is 1.4 g. /-Super.

なお上限は特1こもうけないがフラックス成分組成など
から考えて1.8g/i程度よりも大きくなることはな
い。
Note that the upper limit is not particularly high, but considering the flux component composition, etc., it will not be greater than about 1.8 g/i.

またこの場合のかさ密度は疎充填法によって測定したも
ので具体的1こはJISK67211966の「塩化ビ
ニル樹脂試験方法のかさ比重の測定法−」1こ準じて測
定した。
The bulk density in this case was measured by a loose packing method, specifically in accordance with JIS K67211966 "Method for measuring bulk specific gravity in vinyl chloride resin testing method".

なお本発明フラックスにおいては上記添加成分1こより
十分その性能は満足できるが、靭性、流動性および融点
の調整の目的で、さら1こT 102 。
In the flux of the present invention, the performance can be sufficiently satisfied with one of the above additive components, but one additional component T 102 is added for the purpose of adjusting toughness, fluidity, and melting point.

Ba0Zr02およびに20.Na2O,LiO2を必
要)こ応じて1種又は2種以上の合計が10%以下まで
添加することができる。
Ba0Zr02 and 20. Na2O, LiO2 (necessary) may be added accordingly, up to a total amount of 10% or less of one or more of them.

まずTlO2は切欠き靭性を高めるため1こ有効である
が、3%を超えるとスラグの剥離性が悪くなるので3%
以下が適当である。
First, 1% TlO2 is effective in increasing notch toughness, but if it exceeds 3%, the slag removability deteriorates, so 3% TlO2 is effective.
The following are appropriate.

BangはZ r 02はスラグの流動性および融点の
調整の目的で使用できるが、5%を超えるとポックマー
ク、スラグ巻込みが発生しやすくなり、ビード外観も悪
くなるので5%以下が良い。
Bang says that Zr 02 can be used for the purpose of adjusting the fluidity and melting point of the slag, but if it exceeds 5%, pock marks and slag entrainment are likely to occur, and the bead appearance deteriorates, so it is preferably 5% or less.

Na2O,に20あるいはL i02はビード゛外観を
良好にし、またアークを安定させるため)こ好ましいが
、やはり5%を超えると逆1こアークの吹き上げが生じ
、ビード外観が悪くなるので5%以下であることが望ま
しい。
Na2O, 20 or Li02 is preferable (to improve the bead appearance and stabilize the arc), but if it exceeds 5%, the reverse arc will blow up and the bead appearance will worsen, so it should not exceed 5%. It is desirable that

かかる成分組成をもつ本発明フラックス1こよれば、従
来横向溶接で種々問題のあった諸点をすべて解決するこ
とができる。
By using the flux 1 of the present invention having such a component composition, all of the various problems that have conventionally occurred in horizontal welding can be solved.

以下1こ実施例1こついて本発明を述べる。The present invention will be described below with reference to Example 1.

実施例 本発明フラックスおよび比較フラックスを用いてその差
異を確認するため横向潜弧溶接を行ないスラグの剥離性
、ビード表面に発生するポックマークの有無とビード形
状、またX線によるスラグインクルージヨンあるいは溶
接金属の切欠き靭性と酸素量について比較試験を実施し
た。
EXAMPLE In order to confirm the differences between the flux of the present invention and a comparative flux, horizontal submerged arc welding was performed to examine the slag releasability, the presence or absence of pock marks on the bead surface, the bead shape, and the slag inclusions and welding by X-rays. Comparative tests were conducted on the notch toughness and oxygen content of metals.

第5表に供試フラックスの化学成分を示す。Table 5 shows the chemical composition of the sample flux.

F−L〜F−7が本発明フラックスで、F8が比較フラ
ックスである。
F-L to F-7 are the fluxes of the present invention, and F8 is the comparative flux.

なお、F−8はl 2 XI 50メツシユの市販フラ
ックスである。
Note that F-8 is a commercially available flux of 12XI 50 mesh.

F−1〜F−7の本発明フラックスは、いずれも各種粉
状もしくは粒状の原材料を混合溶解し、その溶融物を水
中Fこて冷却させたものであり、それぞれ32×Dメツ
シユに整粒してフラックスのかさ密度を1.4. g
lct&を超えるよう製造したものである。
The fluxes of the present invention F-1 to F-7 are all made by mixing and melting various powdered or granular raw materials, and cooling the melted product in water with an F trowel, and each is sized to a 32 x D mesh. and set the bulk density of the flux to 1.4. g
It is manufactured to exceed lct&.

これらのフラックスを用い第4図1こ示す開先形状(寸
法単位rnr/L)と、第7表の溶接条件と第5図)こ
示す溶接ビードの積層法(図中の数字は積層10を用い
横向潜弧溶接を行なった。
Using these fluxes, the groove shape shown in Fig. 1 (dimensional unit rnr/L), the welding conditions shown in Table 7, and the weld bead lamination method shown in Fig. 5 (the numbers in the figure indicate lamination 10) Lateral submerged arc welding was performed using

その時の試験板およびワイヤの化学成分を第6表1こ示
す。
The chemical composition of the test plate and wire at that time is shown in Table 6.

試験板は5PV−50Q鋼で板厚25閣、巾4、0 O
rILTrt、長さ750rnmの大きさの板2枚を第
4図のよう1こ開先加工を行ない組立て使用した。
The test plate was made of 5PV-50Q steel with a thickness of 25 mm and a width of 4.0 O.
Two plates having a length of 750 nm were assembled and used by cutting a single bevel as shown in FIG. 4.

上述1こ述べた溶接条件を用い、溶接作業性、内部欠陥
の調整あるいは第6図1こ示す要預)こよりFP側の板
表面より2rILrIL下から2mmVノツチシャルピ
ー衝撃試験片を採取した。
Using the welding conditions described above, a 2mm V notch Charpy impact test piece was taken from 2rILrIL below the plate surface on the FP side for welding workability, adjustment of internal defects, or storage required as shown in FIG.

図中Nはノツチ位置を示す。In the figure, N indicates the notch position.

これらの試験結果を第8表1こまとめて示す。The results of these tests are summarized in Table 8.

第8表から明らかな如く本発明フラックスF1〜F−7
は、スラグ剥離性、ビード形状も良くポックマークの発
生もなく、かつスラグインクルージヨンも皆無であり、
また良好な衝撃値が得られ溶接金属の酸素量も少なかっ
た。
As is clear from Table 8, the fluxes of the present invention F1 to F-7
has good slag removability, good bead shape, no pockmarks, and no slag inclusions.
In addition, good impact values were obtained and the amount of oxygen in the weld metal was small.

これ1こ対して比較フラックスF−8はスラグの剥離性
、形状は良いが、ポックマークの発生、衝撃値が低く、
酸素量が高いなどの問題があった。
In contrast, the comparative flux F-8 has good slag releasability and shape, but generates pock marks and has a low impact value.
There were problems such as high oxygen levels.

以上詳述したよう1こ本発明フラックスは、横向潜弧溶
接]こおいてスラグの剥離性が良く、またポックマーク
が存在せず、良好なビード外観が得られるのみでなく、
スラグインクルージヨンもなく溶接部の切欠き靭性も高
く、横向潜弧溶接用フラックスとして工業的価値はきわ
めて高い。
As detailed above, the flux of the present invention not only has good slag releasability in horizontal submerged arc welding, is free from pockmarks, and provides a good bead appearance;
It has no slag inclusions and has high notch toughness in welded parts, so it has extremely high industrial value as a flux for horizontal submerged arc welding.

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

第1図はS 102 + Al、203 +Ca F2
の成分範囲調査)こ用いた開先形状、寸法を示す模式図
、第2図はS i 02+Al2O3+CaF2の成分
範囲調査1こ用いた溶接ビードの積層順を示す模式図、
第3図はS i02 + Aj!! 203 + Ca
F2添加量と溶着金属の拡散性水素量の関係図、第4
図は実施例]こ用いた開先形状、寸法を示す模式図、第
5図は実施例(こおける溶接ビードの積層順を示す模式
図、第6図は実施例に用いた衝撃試験片の採取要領を示
す模式図である。
Figure 1 shows S 102 + Al, 203 + Ca F2
Fig. 2 is a schematic diagram showing the composition range investigation of S i 02 + Al2O3 + CaF2 (component range investigation 1) showing the groove shape and dimensions used here, and Fig. 2 is a schematic diagram showing the stacking order of the weld bead used
Figure 3 shows S i02 + Aj! ! 203 + Ca
Relationship diagram between the amount of F2 added and the amount of diffusible hydrogen in the weld metal, No. 4
The figure is a schematic diagram showing the shape and dimensions of the groove used in the example. Figure 5 is a schematic diagram showing the stacking order of weld beads in the example. Figure 6 is a schematic diagram showing the stacking order of the weld beads in the example. It is a schematic diagram showing a collection procedure.

Claims (1)

【特許請求の範囲】[Claims] I 5i0221%〜30%、MnO3〜15%、C
aO3〜15%、N12032I〜30%、CaF22
0〜30%を必須成分としS 102 +A l 20
3 +CaF2−68〜83%であり、且つMgOを2
%未満とし、かさ密度が1.4.!i2/c111.超
であることを特徴とする横向潜弧溶接用メルトフラック
ス。
I5i0221%~30%, MnO3~15%, C
aO3~15%, N12032I~30%, CaF22
S 102 +A l 20 with 0 to 30% as essential components
3 +CaF2-68 to 83%, and MgO to 2
%, and the bulk density is 1.4. ! i2/c111. A melt flux for horizontal submerged arc welding that is characterized by its super strength.
JP17242779A 1979-12-27 1979-12-27 Melt flux for horizontal submerged arc welding Expired JPS5852476B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP17242779A JPS5852476B2 (en) 1979-12-27 1979-12-27 Melt flux for horizontal submerged arc welding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP17242779A JPS5852476B2 (en) 1979-12-27 1979-12-27 Melt flux for horizontal submerged arc welding

Publications (2)

Publication Number Publication Date
JPS5692000A JPS5692000A (en) 1981-07-25
JPS5852476B2 true JPS5852476B2 (en) 1983-11-22

Family

ID=15941762

Family Applications (1)

Application Number Title Priority Date Filing Date
JP17242779A Expired JPS5852476B2 (en) 1979-12-27 1979-12-27 Melt flux for horizontal submerged arc welding

Country Status (1)

Country Link
JP (1) JPS5852476B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110293337A (en) * 2019-06-28 2019-10-01 东北大学 One kind low zirconium fluorine alkaline type sintered flux peculiar to vessel and preparation method thereof

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2010117074A1 (en) * 2009-04-10 2010-10-14 新日本製鐵株式会社 Highly basic fused flux for submerged arc welding
JP5627493B2 (en) * 2011-02-08 2014-11-19 日鐵住金溶接工業株式会社 Submerged arc welding method

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110293337A (en) * 2019-06-28 2019-10-01 东北大学 One kind low zirconium fluorine alkaline type sintered flux peculiar to vessel and preparation method thereof

Also Published As

Publication number Publication date
JPS5692000A (en) 1981-07-25

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