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JPH0237833B2 - SABUMAAJIAAKUYOSETSUYOSHOSEIFURATSUKUSU - Google Patents
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JPH0237833B2 - SABUMAAJIAAKUYOSETSUYOSHOSEIFURATSUKUSU - Google Patents

SABUMAAJIAAKUYOSETSUYOSHOSEIFURATSUKUSU

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Publication number
JPH0237833B2
JPH0237833B2 JP8414785A JP8414785A JPH0237833B2 JP H0237833 B2 JPH0237833 B2 JP H0237833B2 JP 8414785 A JP8414785 A JP 8414785A JP 8414785 A JP8414785 A JP 8414785A JP H0237833 B2 JPH0237833 B2 JP H0237833B2
Authority
JP
Japan
Prior art keywords
alumina
flux
amount
weight
water glass
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 - Lifetime
Application number
JP8414785A
Other languages
Japanese (ja)
Other versions
JPS61242789A (en
Inventor
Isao Sugioka
Saneji Nishimura
Masao Kamata
Kaneo Kumagai
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 JP8414785A priority Critical patent/JPH0237833B2/en
Publication of JPS61242789A publication Critical patent/JPS61242789A/en
Publication of JPH0237833B2 publication Critical patent/JPH0237833B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

(産業上の利用分野) 本発明は軟鋼、高張力鋼、低合金鋼あるいはス
テンレス鋼などの鋼の溶接に一般的に使用されて
いる、水ガラスを添加して造粒後焼成される吸湿
性を低く抑えうるサブマージアーク溶接用焼成フ
ラツクスに関する。 (従来の技術) 現在、鋼の自動溶接法としてはサブマージアー
ク溶接法が広く使われている。このサブマージア
ーク溶接用フラツクス(以下フラツクスという)
には各種の原材料を電気炉で溶融して冷却、粉
砕、製粒してなるいわゆる溶融型フラツクスと、
各種の細粒の原料を水ガラスで造粒して400℃〜
900℃の温度で焼成するいわゆる焼成フラツクス
とがある。 このうち焼成フラツクスは最近の各種の品質ア
ツプの要求に対し、高塩基性組成のものが容易に
得られること、かつ原材料中に炭酸塩を含有させ
うることによりより低水素化が達成できること、
さらには脱酸剤、合金剤が容易に添加できること
などその組成面での自由度が大きく、広く利用さ
れつつある。 しかしながら、この焼成フラツクスの最大の問
題点は造粒のための固着剤として水ガラスを使用
することである。従来、水ガラスを添加して造粒
した後400℃〜600℃の焼成を行なつたフラツクス
では、缶に密封されていた状態から溶接時に開缶
され、大気中に放置されると、水分の吸湿が著し
く、10時間以上大気中に放置されると、例えば1
重量%程度の吸湿量がみられる。このような場
合、そのまま溶接されるとその吸湿水分によつて
溶接部にピツトやブローホールが生じたり、ある
いは拡散性水素量の増加により溶接部に水素割れ
が生ずるなど問題が生ずることになる。 この吸湿現象は明らかに水ガラスの吸湿性にも
とづくものであり、この吸湿性をできるだけ少な
くするため、従来例えば特開昭55−133899号公報
にみられるような(SiO2/アルカリ酸化物)の
モル比と(K2O/Na2O+K2O)のモル比を制限
した水ガラス組成の検討などがなされてきている
が、十分な効果は得られず、実際には使用時フラ
ツクスの吸湿管理に多大な注意がはらわれている
のが現状である。 (発明が解決しようとする問題点) 本発明は、この固着剤として水ガラスを使用す
る焼成フラツクスの水ガラス添加量を大幅に少な
くでき、その結果フラツクスの吸湿性を非常に少
なくした焼成型フラツクスを提供する。 (問題点を解決するための手段) 本発明の要旨は、アルミナを50重量%以下含有
するサブマージアーク溶接用焼成フラツクスにお
いて、焼成前の原料に粒子径10μm以下の微細粒
アルミナを3重量%以上含有し、かつ平均粒子径
が40〜100μmの粗粒アルミナの含有量が15重量
%以下であることを特徴とするサブマージアーク
溶接用焼成フラツクスである。 (作用) 以下、本発明について詳細に説明する。 本発明者らは高張力鋼、低温用鋼、さらには高
合金鋼などの溶接に一般的によく使用されてい
る、アルミナを3〜50重量%含有し、その他に SiO2 5〜40重量%、 TiO2 0〜35重量%、 CaO 10〜50重量%、 MgO 15〜50重量%、 BaO 0〜25重量%、 アルカリ金属酸化物 2〜10重量%、 CO2 0〜20重量%、 金属弗化物 3〜60重量%、 金属粉 0〜50重量% を含有する焼成フラツクスについて、円筒内に高
速回転するプロペラ状の羽根をもつヘンシエル高
速造粒機を用いて、吸湿水分量を少なくするた
め、如何に水ガラス量を少なくして造粒でき、か
つ焼成後の粒子強度を大きく保ちうるかについ
て、主に原材料の粒度構成について種々検討し
た。 その結果、アルミナ原材料として、従来から使
用されている標準粒のアルミナに代えて微細粒化
したものを使用することによつて、水ガラス添加
量が大幅に低減できること、かつ焼成後の粒子強
度も十分になることが明らかとなつた。これによ
つて焼成フラツクスの吸湿量を従来の半分程度に
まで低減することが可能となつた。 アルミナは水酸化アルミニウムを焼成すること
によつてできる白色粉末結晶で、顕微鏡下で観察
すると微細なα結晶粒(コランダム)が多数凝集
した粒子としてみることができる。 溶接フラツクス用として従来から使用されてい
るのはこの数μmのα結晶粒が多数凝集した粒子
の平均粒子径が40〜100μmの粗粒アルミナで、
これはいわば多孔質状のものであり、平均粒子径
の大きさに比し比表面積が大きく、造粒時水ガラ
スを多く必要とするわりにフラツクス粒子の凝集
化(造粒)にはあまり水ガラスが有効に働かない
と考えられる。 一方、本発明でいう微細粒のアルミナとは、平
均粒子径を小さく、α結晶粒径に近い1〜10μm
に細かくしたものであり、多孔質の状態が少なく
なつたいわばα結晶粒そのものがアルミナ粒子で
あることを意味し、その比表面積があまり変化せ
ずに微細粒化した状態になつている。従つて水ガ
ラス添加時のフラツクス粒子の凝集力がアルミナ
粒子の微細化により大きくなるとともに、水ガラ
スが有効に働くためにその添加量が非常に少なく
ても容易に造粒し易くなる。造粒後焼成してフラ
ツクスの粉化試験を行ない、フラツクスの粒子強
度を測定したが、水ガラスが造粒に有効に働いて
いるため、フラツクスの粒子強度が劣化しないこ
とが明らかとなつた。 以下に数値限定理由をのべる。 前述したごとくアルミナは水酸化アルミニウム
を高温で焼成して安定なαアルミナ結晶粒の集合
体として作られるが、一般に見かけの粒度(α結
晶の凝集粒)とαアルミナ結晶粒弐大きさの両方
が製造条件によつてコントロールされる。このう
ち、α結晶粒の大きさは焼成温度と時間によつて
変化するものであるが、通常10μm以下のものと
なる。本発明でアルミナ粒子径を10μm以下とし
たのは、α結晶粒の凝集した粒を粉砕によつてほ
ぐしてアルミナ粒子径をできるだけαアルミナ結
晶粒径に近づけることにより多孔質性をできるだ
け少なくするためであり、これにより水ガラス添
加量を少なくできる効果が生ずることになる。さ
らに、10μm以上の粒子径のものが大部分を占め
る他のフラツクス原材料に10μm以下の微細粒ア
ルミナが混合されることにより、水ガラスを添加
して造粒しようとする場合、造粒性が良好になる
効果も加わり、さらに水ガラス量を少なくするこ
とができることになる。 フラツクス中へのこの微細粒アルミナの含有量
としては3重量%以上でその効果が明確になり、
その効果は、本発明者らが実験したアルミナを50
%まで含有させたフラツクスにおいて、全量この
微細粒アルミナに置換した場合も有効であつた。 しかし、この場合の粗粒アルミナの含有量につ
いては、15重量%以下でなければならない。粗粒
アルミナは前記のようにいわば多孔質状のもので
あり、15重量%を超えて含有させると造粒時の水
ガラスの添加量が多くなり、フラツクスの吸湿量
をピツト、ブローホール、あるいは水素割れなど
の発生防止に必要な1重量%以下にすることが困
難になる。 なお本発明は水ガラス添加量の減少により吸湿
性を減少させるものであり、水ガラスの組成は目
的に応じて自由に調整できLi2O系の低吸湿性の
水ガラス使用も勿論可能である。 (実施例) 表1に示すような標準粒のアルミナを含む原材
料からなる4種の組成のフラツクス(No.1、No.
5、No.7およびNo.10)のアルミナを微細粒アルミ
ナに一部又は全部置換した原料に水ガラスを添加
して造粒した。そのときの造粒に要した水ガラス
必要量を同表最右欄に記した。 なお、使用した標準粒のアルミナは粒径74μm
以上32%、44μm以上77%、10μm以下3%のも
の(平均粒子径の代表値として60μm、α結晶粒
径3μmとして提示されているもの)であり、ま
た微細粒アルミナは粒径10μm以下95%、4μm以
下86%、2μm以下55%のもの(平均粒子径の代
表として2μm、α結晶粒径0.3〜3μmとして提示
されているもの)を使用した。 造粒の固着剤として使用した水ガラスは
SiO228、Na2O10、K2O4比からなる40ボーメの
ものである。 造粒は高速回転のヘンシエルミキサーを使用
し、造粒時間は約1〜2分でいずれも完了してい
る。これらのNo.1〜No.11までのフラツクスは造粒
後250℃で短時間ロータリーキルン中で乾燥した
後、480℃〜500℃、1時間焼成後、12×100メツ
シユ(1410μm〜149μm)に造粒した。 これらのフラツクスは吸湿試験と粉化(粒子強
度)試験を行なつた。吸湿試験は雰囲気として30
℃、80%相対湿度の恒温恒湿炉中でフラツクス厚
さ20mmで実施し、24時間後の吸湿水分重量を測定
した。また、粉化試験は、フラツクス50gを直径
8mmの鉄球9個とともに内径40mm、長さ300mmの
円筒型容器に入れ、容器の両端部中心から軸線方
向150mmの点を中心としてその点を通り円筒軸に
直交する線の周りに30回転/分の回転数で30分間
回転させた後、149μmより小さい粒子の増加量
(重量%)を測定し、それを粒子強度とした。こ
れらの試験の結果を表2および第1図に示す。 表2中に示したように、微細粒アルミナの添加
によつて水ガラス添加量が減少できた。No.2、
3、4(ベースNo.1)、No.6(ベースNo.5)、No.8

9(ベースNo.7)、No.11(ベースNo.10)の吸湿量は
それぞれのベースのものに比べてほぼ水ガラス添
加量に比例して減少しており、微細粒アルミナの
添加量によつては使用しないものにくらべ約50%
まで低下させることが可能であつた。 また、粉化量については水ガラス量の差にほと
んど関係なく少なく、いずれも問題のないことが
明らかである。 なお、第1図は実施例における各フラツクスに
ついて、フラツクスの吸湿量に及ぼす微細粒アル
ミナの含有量と粗粒アルミナの含有量の影響を示
したものである。微細粒アルミナが3重量%以上
で、かつ粗粒アルミナが15重量%以下の範囲にお
いてフラツクスの吸湿量を1重量%以下に減少さ
せることができる。
(Industrial Application Field) The present invention is a hygroscopic material that is commonly used for welding steels such as mild steel, high-strength steel, low-alloy steel, or stainless steel. The present invention relates to a sintered flux for submerged arc welding that can keep the temperature low. (Prior Art) Submerged arc welding is currently widely used as an automatic welding method for steel. This flux for submerged arc welding (hereinafter referred to as flux)
There are so-called molten fluxes, which are made by melting various raw materials in an electric furnace, cooling them, crushing them, and granulating them.
Various fine grain raw materials are granulated with water glass and heated to 400℃~
There is a so-called fired flux that is fired at a temperature of 900°C. Of these, calcined fluxes meet the recent demands for improved quality, with the following advantages: a highly basic composition can be easily obtained, and low hydrogenation can be achieved by incorporating carbonate into the raw material;
Furthermore, it has a great degree of freedom in terms of composition, such as the ability to easily add deoxidizers and alloying agents, and is becoming widely used. However, the biggest problem with this calcined flux is the use of water glass as a sticking agent for granulation. Conventionally, fluxes that are granulated with water glass and then fired at 400°C to 600°C lose moisture when they are sealed in cans, opened during welding, and left in the atmosphere. If the moisture absorption is significant and it is left in the atmosphere for more than 10 hours, for example, 1
The amount of moisture absorbed is approximately % by weight. In such a case, if welding is continued as is, problems such as pits or blowholes will occur in the welded area due to the absorbed moisture, or hydrogen cracking will occur in the welded area due to an increase in the amount of diffusible hydrogen. This moisture absorption phenomenon is clearly based on the hygroscopicity of water glass, and in order to reduce this hygroscopicity as much as possible, conventional methods such as (SiO 2 /alkali oxide) as seen in JP-A-55-133899 have been used. Studies have been conducted on water glass compositions that limit the molar ratio (K 2 O / Na 2 O + K 2 O), but sufficient effects have not been obtained, and in reality, it is difficult to manage the moisture absorption of flux during use. Currently, a great deal of attention is being paid to (Problems to be Solved by the Invention) The present invention provides a fired flux in which the amount of water glass added to the fired flux using water glass as a fixing agent can be significantly reduced, and as a result, the hygroscopicity of the flux is extremely reduced. I will provide a. (Means for Solving Problems) The gist of the present invention is that, in a fired flux for submerged arc welding containing 50% by weight or less of alumina, 3% by weight or more of fine-grained alumina with a particle size of 10 μm or less is added to the raw material before firing. The fired flux for submerged arc welding is characterized in that the content of coarse-grained alumina having an average particle diameter of 40 to 100 μm is 15% by weight or less. (Function) Hereinafter, the present invention will be explained in detail. The present inventors have found that alumina, which is commonly used for welding high-strength steel, low-temperature steel, and even high-alloy steel, is contained in an amount of 3 to 50% by weight, and in addition, SiO 2 is contained in an amount of 5 to 40% by weight. , TiO 2 0-35% by weight, CaO 10-50% by weight, MgO 15-50% by weight, BaO 0-25% by weight, alkali metal oxide 2-10% by weight, CO 2 0-20% by weight, metal fluoride In order to reduce the amount of moisture absorbed by using a Henschel high-speed granulator, which has propeller-like blades that rotate at high speed in a cylinder, for the fired flux containing 3 to 60% by weight of chemical compounds and 0 to 50% by weight of metal powder, Various studies were conducted, mainly regarding the particle size structure of the raw materials, in order to find out how to reduce the amount of water glass for granulation and maintain a high particle strength after firing. As a result, by using fine-grained alumina as an alumina raw material instead of the conventionally used standard-grained alumina, the amount of water glass added can be significantly reduced, and the particle strength after firing can also be improved. It became clear that this would be sufficient. This has made it possible to reduce the amount of moisture absorbed by the fired flux to about half that of the conventional method. Alumina is a white powder crystal produced by firing aluminum hydroxide, and when observed under a microscope, it can be seen as agglomerated particles of many fine α-crystal grains (corundum). What has traditionally been used for welding flux is coarse-grained alumina, in which many α-crystal grains of several μm are aggregated, and the average particle diameter is 40 to 100 μm.
This is porous, so to speak, and has a large specific surface area compared to the average particle size, and although a large amount of water glass is required during granulation, it is not sufficient for agglomeration (granulation) of flux particles. is considered not to work effectively. On the other hand, fine-grained alumina in the present invention has a small average particle size, 1 to 10 μm, which is close to the α crystal grain size.
This means that the α-crystal grains themselves are alumina particles, which means that the porous state is reduced, and the specific surface area does not change much and is in a fine-grained state. Therefore, the cohesive force of the flux particles when water glass is added increases due to the finer alumina particles, and since the water glass works effectively, it becomes easier to granulate the flux particles even if the amount added is very small. After granulation and firing, the flux was subjected to a pulverization test and the particle strength of the flux was measured, and it was found that the particle strength of the flux did not deteriorate because the water glass was working effectively in granulation. The reasons for the numerical limitations are listed below. As mentioned above, alumina is produced as an aggregate of stable α-alumina crystal grains by firing aluminum hydroxide at high temperatures, but generally both the apparent particle size (agglomerated grains of α-crystals) and the size of the α-alumina crystal grains are Controlled by manufacturing conditions. Among these, the size of the α crystal grains varies depending on the firing temperature and time, but is usually 10 μm or less. The reason why the alumina particle size is set to 10 μm or less in the present invention is to reduce porosity as much as possible by loosening the agglomerated α crystal grains by crushing and making the alumina particle size as close to the α alumina crystal grain size as possible. This results in the effect of reducing the amount of water glass added. Furthermore, since fine alumina particles of 10 μm or less are mixed with other flux raw materials, most of which have particle diameters of 10 μm or more, granulation performance is good when granulation is attempted by adding water glass. In addition, the amount of water glass can be further reduced. The effect becomes clear when the content of fine alumina in the flux is 3% by weight or more.
The effect is that the alumina tested by the present inventors is 50%
It was also effective when the entire amount of the flux was replaced with this fine-grained alumina. However, the content of coarse alumina in this case must be 15% by weight or less. As mentioned above, coarse-grained alumina is porous, and if it is contained in an amount exceeding 15% by weight, the amount of water glass added during granulation increases, and the amount of moisture absorbed by the flux is reduced by pits, blowholes, or It becomes difficult to reduce the content to 1% by weight or less, which is necessary to prevent hydrogen cracking and the like. Note that the present invention reduces hygroscopicity by reducing the amount of water glass added, and the composition of water glass can be freely adjusted depending on the purpose, and of course it is also possible to use Li 2 O-based water glass with low hygroscopicity. . (Example) Fluxes with four compositions (No. 1, No.
5, No. 7, and No. 10) in which the alumina was partially or completely replaced with fine-grained alumina, water glass was added to the raw materials and granulated. The required amount of water glass required for granulation at that time was recorded in the rightmost column of the same table. The standard grain alumina used has a grain size of 74 μm.
32% or more, 77% of 44μm or more, and 3% of 10μm or less (representative values of average particle size are 60μm and alpha grain size of 3μm), and fine grain alumina has a grain size of 10μm or less95 %, 86% of 4 μm or less, 55% of 2 μm or less (representative of average particle diameter is 2 μm, and α crystal grain size is presented as 0.3 to 3 μm). Water glass used as a fixing agent for granulation
It is of 40 Baume, consisting of SiO 2 28, Na 2 O 10, K 2 O4 ratio. Granulation was performed using a high-speed rotating Henschel mixer, and the granulation time was approximately 1 to 2 minutes. After granulation, these fluxes No. 1 to No. 11 were dried in a rotary kiln at 250°C for a short time, then fired at 480°C to 500°C for 1 hour, and then formed into 12 × 100 meshes (1410 μm to 149 μm). It was grainy. These fluxes were subjected to moisture absorption tests and dusting (particle strength) tests. Moisture absorption test is conducted with an atmosphere of 30
The test was carried out with a flux thickness of 20 mm in a constant temperature and humidity oven at 80% relative humidity and the weight of absorbed moisture was measured after 24 hours. In addition, in the powdering test, 50 g of flux was placed in a cylindrical container with an inner diameter of 40 mm and a length of 300 mm together with nine iron balls of 8 mm in diameter, and a cylindrical tube was passed through the center at a point 150 mm in the axial direction from the center of both ends of the container. After rotating for 30 minutes around a line perpendicular to the axis at a rotation speed of 30 revolutions/minute, the increase in the amount of particles smaller than 149 μm (% by weight) was measured, and this was taken as the particle strength. The results of these tests are shown in Table 2 and FIG. As shown in Table 2, the addition of fine alumina reduced the amount of water glass added. No.2,
3, 4 (Base No. 1), No. 6 (Base No. 5), No. 8
,
The moisture absorption amount of No. 9 (Base No. 7) and No. 11 (Base No. 10) decreased in proportion to the amount of water glass added compared to those of each base, and the amount of moisture absorbed by No. 9 (Base No. 7) and No. 11 (Base No. 10) decreased in proportion to the amount of water glass added. Approximately 50% less than those that are not used
It was possible to reduce it to Moreover, the amount of powdering is small regardless of the difference in the amount of water glass, and it is clear that there is no problem in either case. Note that FIG. 1 shows the influence of the content of fine alumina and the content of coarse alumina on the amount of moisture absorbed by the flux for each flux in Examples. When the amount of fine alumina is 3% by weight or more and the amount of coarse alumina is 15% by weight or less, the amount of moisture absorbed by the flux can be reduced to 1% by weight or less.

【表】【table】

【表】 (発明の効果) 以上の結果から明らかなごとく、本発明フラツ
クスを用いれば水ガラスにもとづく吸湿性を大幅
に減少することが可能となり、それらのフラツク
スの使用により現場での使用時の吸湿管理が容易
になるとともに、溶接時水分吸湿にもとづくピツ
ト、ブローホールの発生や、水素割れの発生を防
止することが可能となる。
[Table] (Effects of the invention) As is clear from the above results, the use of the fluxes of the present invention makes it possible to significantly reduce the hygroscopicity caused by water glass, and the use of these fluxes makes it possible to reduce the hygroscopicity during on-site use. Moisture absorption management becomes easier, and it becomes possible to prevent the occurrence of pits and blowholes due to moisture absorption during welding, as well as hydrogen cracking.

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

第1図は実施例におけるフラツクスの吸湿試験
結果を示す図である。
FIG. 1 is a diagram showing the results of a moisture absorption test on flux in Examples.

Claims (1)

【特許請求の範囲】[Claims] 1 アルミナを50重量%以下含有するサブマージ
アーク溶接用焼成フラツクスにおいて、焼成前の
原料に粒子径10μm以下の微細粒アルミナを3重
量%以上含有し、かつ平均粒子径が40〜100μm
の粗粒アルミナの含有量が15重量%以下であるこ
とを特徴とするサブマージアーク溶接用焼成フラ
ツクス。
1 In the fired flux for submerged arc welding containing 50% by weight or less of alumina, the raw material before firing contains 3% by weight or more of fine-grained alumina with a particle size of 10 μm or less, and the average particle size is 40 to 100 μm.
A fired flux for submerged arc welding, characterized in that the content of coarse-grained alumina is 15% by weight or less.
JP8414785A 1985-04-19 1985-04-19 SABUMAAJIAAKUYOSETSUYOSHOSEIFURATSUKUSU Expired - Lifetime JPH0237833B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP8414785A JPH0237833B2 (en) 1985-04-19 1985-04-19 SABUMAAJIAAKUYOSETSUYOSHOSEIFURATSUKUSU

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP8414785A JPH0237833B2 (en) 1985-04-19 1985-04-19 SABUMAAJIAAKUYOSETSUYOSHOSEIFURATSUKUSU

Publications (2)

Publication Number Publication Date
JPS61242789A JPS61242789A (en) 1986-10-29
JPH0237833B2 true JPH0237833B2 (en) 1990-08-27

Family

ID=13822385

Family Applications (1)

Application Number Title Priority Date Filing Date
JP8414785A Expired - Lifetime JPH0237833B2 (en) 1985-04-19 1985-04-19 SABUMAAJIAAKUYOSETSUYOSHOSEIFURATSUKUSU

Country Status (1)

Country Link
JP (1) JPH0237833B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022030159A1 (en) * 2020-08-03 2022-02-10 株式会社神戸製鋼所 Welding flux and production method therefor, and submerged arc welding method using same welding flux

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2022030159A1 (en) * 2020-08-03 2022-02-10 株式会社神戸製鋼所 Welding flux and production method therefor, and submerged arc welding method using same welding flux

Also Published As

Publication number Publication date
JPS61242789A (en) 1986-10-29

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