Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JP5146998B2 - Fused flux for submerged arc welding - Google Patents
[go: Go Back, main page]

JP5146998B2 - Fused flux for submerged arc welding - Google Patents

Fused flux for submerged arc welding Download PDF

Info

Publication number
JP5146998B2
JP5146998B2 JP2007316223A JP2007316223A JP5146998B2 JP 5146998 B2 JP5146998 B2 JP 5146998B2 JP 2007316223 A JP2007316223 A JP 2007316223A JP 2007316223 A JP2007316223 A JP 2007316223A JP 5146998 B2 JP5146998 B2 JP 5146998B2
Authority
JP
Japan
Prior art keywords
amount
oxygen
slag
flux
viscosity
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 - Fee Related
Application number
JP2007316223A
Other languages
Japanese (ja)
Other versions
JP2009136898A (en
Inventor
浩久 田邉
昌彦 濱田
隆之 西
方史 花尾
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 and Sumitomo Metal 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 and Sumitomo Metal Corp filed Critical Nippon Steel and Sumitomo Metal Corp
Priority to JP2007316223A priority Critical patent/JP5146998B2/en
Publication of JP2009136898A publication Critical patent/JP2009136898A/en
Application granted granted Critical
Publication of JP5146998B2 publication Critical patent/JP5146998B2/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Landscapes

  • Nonmetallic Welding Materials (AREA)

Description

本発明は、サブマージアーク溶接時に使用される溶融型フラックスに関する。   The present invention relates to a melt type flux used during submerged arc welding.

サブマージアーク溶接用フラックスは、溶接に際して溶融スラグを形成することにより溶融金属を大気から遮断し溶接金属の窒化、酸化を防ぐとともに、スラグ/メタル反応を介して溶融金属と冶金反応を行い短時間で清浄な溶接金属を作り、良好なビードを形成する等の重要な働きを持っている。   Flux for submerged arc welding forms molten slag during welding to block molten metal from the atmosphere to prevent nitridation and oxidation of the weld metal and to perform metallurgical reaction with molten metal via slag / metal reaction in a short time. It has important functions such as making clean weld metal and forming good beads.

溶接金属に求められる特性として強度と靭性が挙げられるが、一般に強度と靱性とは相反する特性であるため、強度が増加するほど靱性の確保が困難になる。この課題に対応するためには溶接金属酸素量の低減が有効であることが知られており、種々の成分を有する溶融型フラックスが、例えば特許文献1〜11等に開示されている。いずれの文献においても、フラックス中の塩基性成分および酸性成分の調整による酸素量の低減(あるいは溶接金属靱性の改善)、および配合比の調整による溶接性確保の観点から提案がなされている。   Strength and toughness are listed as properties required for weld metal, but generally, strength and toughness are contradictory properties, so that it becomes difficult to ensure toughness as the strength increases. In order to cope with this problem, it is known that reduction of the amount of weld metal oxygen is effective, and molten fluxes having various components are disclosed in, for example, Patent Documents 1 to 11. In any literature, proposals have been made from the viewpoint of reducing the oxygen content (or improving the weld metal toughness) by adjusting the basic component and the acidic component in the flux, and securing weldability by adjusting the compounding ratio.

溶接金属酸素量を低減するには、SiO量を少なくすると共にフラックス中の塩基性成分量を高くする方法が一般に知られている。例えば、特許文献5には低SiO−高CaF系フラックスとすることにより、溶接金属酸素量を低減する技術が開示されている。 In order to reduce the amount of weld metal oxygen, generally known is a method of reducing the amount of SiO 2 and increasing the amount of basic components in the flux. For example, Patent Document 5 discloses a technique for reducing the amount of weld metal oxygen by using a low SiO 2 -high CaF 2 flux.

一方、溶接欠陥のない良好な溶接を行うためには、一般に、溶融池の形状を一定に保ちながら溶接を行う必要がある。サブマージアーク溶接の場合、溶融池は溶融スラグに常に覆われた状態であるため、溶融池形状の安定化には溶融スラグの高温物性、特に溶融スラグ粘度が重要な因子となる。サブマージアーク溶接のような大電流溶接ではアーク圧力により溶融池形状が乱されるため、この乱れを抑止するには溶融池を覆う溶融スラグの粘度が高い方が良い。この点に関し、特許文献12にはスラグ粘度に着目した高速溶接性に優れたフラックスが開示されている。
特開平6−31481号公報 特開平6−285679号公報 特開平7−256488号公報 特開平7−303990号公報 特開平8−187593号公報 特開平9−85488号公報 特開平9−262692号公報 特開平11−277294号公報 特開2004−154840号公報 特開2005−125345号公報 特開2005−329462号公報 特開平11−19795号公報
On the other hand, in order to perform good welding without welding defects, it is generally necessary to perform welding while keeping the shape of the molten pool constant. In the case of submerged arc welding, since the molten pool is always covered with molten slag, the high-temperature physical properties of the molten slag, particularly the molten slag viscosity, is an important factor for stabilizing the molten pool shape. In high current welding such as submerged arc welding, the molten pool shape is disturbed by the arc pressure. Therefore, the viscosity of the molten slag covering the molten pool is preferably high in order to suppress this disturbance. In this regard, Patent Document 12 discloses a flux excellent in high-speed weldability focusing on slag viscosity.
JP-A-6-31481 JP-A-6-285679 JP 7-256488 A Japanese Patent Laid-Open No. 7-303990 JP-A-8-187593 JP-A-9-85488 Japanese Patent Laid-Open No. 9-262692 Japanese Patent Laid-Open No. 11-277294 JP 2004-154840 A JP 2005-125345 A JP 2005-329462 A JP-A-11-19795

ところが、特許文献12では溶接金属酸素量についてはなんら検討されていない。これは、次の理由による。 前述したように、溶接金属酸素量を低減するには塩基性成分量を高くすることが必要となるが、高塩基性スラグは粘度が低いため、溶融池の乱れが大きくなりアンダーカットやスラグ巻き込み等の溶接欠陥が発生しやすくなる。つまり、溶接金属酸素量低減と耐溶接欠陥性とは相反の関係にある。このため、特許文献12では、双方のバランスを図るのではなく、相反する因子のうちの一方のみの改善に特化したものと考えられる。   However, Patent Document 12 does not discuss the amount of weld metal oxygen. This is due to the following reason. As mentioned above, it is necessary to increase the amount of basic components in order to reduce the amount of oxygen in the weld metal. However, because the viscosity of high basic slag is low, the turbulence of the molten pool increases, causing undercuts and slag entrainment. Such a welding defect is likely to occur. That is, there is a reciprocal relationship between the weld metal oxygen content reduction and the weld defect resistance. For this reason, in patent document 12, it is thought that it was specialized in the improvement of only one of the conflicting factors rather than trying to balance both.

このように、従来のフラックス塩基度に基づく成分調整では、溶接金属酸素量低減と耐溶接欠陥性とのバランスを取ることは容易でない。低酸素化と耐溶接欠陥性向上とを両立するためには、フラックス成分および溶融スラグ粘度を厳密に制御することが求められ、例えば、特許文献5では、複数の成分の相互関係を厳密に規定している。こうした対応が生産性の低下につながることはいうまでもない。   Thus, in the conventional component adjustment based on the flux basicity, it is not easy to balance the reduction in the amount of weld metal oxygen and the resistance to weld defects. In order to achieve both low oxygen and improved weld defect resistance, it is required to strictly control the flux component and the molten slag viscosity. For example, in Patent Document 5, the mutual relationship between a plurality of components is strictly defined. doing. It goes without saying that such a response leads to a decline in productivity.

そこで、本発明では、従来のフラックス塩基度に基づく成分調整とは異なる視点での検討を行い、溶接金属酸素量低減と耐溶接欠陥性を両立可能なサブマージアーク溶接用溶融型フラックスを提供することを目的とする。   In view of this, the present invention provides a molten flux for submerged arc welding that can perform both a reduction in the amount of oxygen in the weld metal and resistance to weld defects by conducting a study from a different viewpoint than the conventional component adjustment based on flux basicity. With the goal.

本発明者らは、まず、サブマージアーク溶接金属の酸素量を低減するべく、フラックス組成の溶接金属酸素量への影響に関する考察を行った。具体的には、フラックスが同一成分の溶融スラグを形成すると仮定して、溶融スラグと溶融金属との間の酸素の分配平衡を熱力学的に推定し、その影響を考察した。一般的な溶接反応は急速昇温、急速冷却の非平衡反応であるが、サブマージアーク溶接においては高温かつアーク圧力による強攪拌状態にある。そこで、溶融スラグ/メタル間に平衡が成り立つと仮定して熱力学平衡計算によりメタル中溶存酸素量を計算し、溶接金属の酸素量実測値と比較した。その結果、メタル中溶存酸素量計算値と溶接金属酸素量の実測値とが相関していることを見出し、溶接金属の酸素量を低減するためにはフラックス組成を低酸素ポテンシャル成分系にする、つまりスラグメタル熱力学平衡計算により得られるメタル中溶存酸素量が低くなる成分系にすることが重要であることを見出した。   In order to reduce the oxygen content of the submerged arc weld metal, the present inventors first considered the influence of the flux composition on the weld metal oxygen content. Specifically, assuming that the flux forms molten slag of the same component, the oxygen distribution equilibrium between the molten slag and the molten metal was estimated thermodynamically, and the effect was considered. The general welding reaction is a non-equilibrium reaction of rapid temperature rise and rapid cooling, but in submerged arc welding, it is in a state of strong stirring due to high temperature and arc pressure. Therefore, the amount of dissolved oxygen in the metal was calculated by thermodynamic equilibrium calculation, assuming that an equilibrium was established between the molten slag / metal, and compared with the measured oxygen amount of the weld metal. As a result, it was found that the calculated amount of dissolved oxygen in the metal and the measured value of the amount of oxygen in the weld metal were correlated, and in order to reduce the amount of oxygen in the weld metal, the flux composition was made a low oxygen potential component system. That is, it was found that it is important to use a component system in which the amount of dissolved oxygen in the metal obtained by slag metal thermodynamic equilibrium calculation is low.

また、耐溶接欠陥性を向上するべく溶融スラグ粘度についても考察した。前述したように、耐溶接欠陥性向上には高スラグ粘度化することが有効であるが、種々の実験、研究を行った結果、低酸素ポテンシャル成分系フラックスにおいても、溶融スラグ粘度が高すぎると酸素量を低減できないことを見出し、酸素量低減可能な溶融スラグ粘度上限値(1500℃)は1.00Poise未満であることを見出した。また、耐溶接欠陥性確保に必要な溶融スラグ粘度下限値は0.1Poise以上であることも合わせて見出した。低酸素ポテンシャル成分系フラックスの高スラグ粘度化により低酸素化が困難となる原因は明らかではないが、スラグ粘度が高すぎると溶接中の溶融スラグ・溶融金属間の攪拌力が弱くなり、溶融スラグ・溶融金属間の酸素分配時における物質移動速度が遅くなるためであると推定される。   In addition, the molten slag viscosity was also considered in order to improve the weld defect resistance. As described above, it is effective to increase the slag viscosity to improve the weld defect resistance. However, as a result of various experiments and researches, if the molten slag viscosity is too high even in a low oxygen potential component flux, It was found that the amount of oxygen could not be reduced, and it was found that the molten slag viscosity upper limit (1500 ° C.) capable of reducing the amount of oxygen was less than 1.00 poise. It was also found that the lower limit value of the melt slag viscosity necessary for ensuring the weld defect resistance is 0.1 Poise or more. The reason why it is difficult to reduce oxygen due to the high slag viscosity of the low oxygen potential component flux is not clear, but if the slag viscosity is too high, the stirring force between the molten slag and molten metal during welding will be weakened, resulting in molten slag.・ It is presumed that the mass transfer rate during oxygen distribution between the molten metals is slow.

以上の知見に基づき、フラックス組成を低酸素ポテンシャル成分系とし、そのうえ1500℃スラグ粘度を0.1Poise以上1.00Poise未満とすることで溶接金属酸素量低減と耐溶接欠陥性向上との両立が可能となる。   Based on the above knowledge, it is possible to achieve both reduced weld metal oxygen content and improved weld defect resistance by setting the flux composition to a low oxygen potential component system and 1500 ° C slag viscosity to 0.1 Poise or more and less than 1.00 Poise. It becomes.

具体的には、耐溶接欠陥性向上に必要であるが溶接金属酸素量を増加させるSiO(高粘度・高酸素ポテンシャル成分)を低くし、代わりに酸素量増加効果の小さくスラグ粘度向上効果を持つAl(高粘度・低酸素ポテンシャル成分)を多量添加する。Al多量添加によるフラックス融点上昇を適正な量のCaF添加により抑制してスラグ流動性を確保しつつ、好ましくはさらにCaO−CaF成分バランスを適正に調整することで低酸素ポテンシャル成分系とし、1500℃スラグ粘度も0.1Poise以上1.00Poise未満とすることで上記課題を解決し、溶接金属酸素量を300ppm未満、好適な態様では250ppm以下、特に好適な態様では200ppm以下にしつつ、ビード外観の劣化、アンダーカット、ポッツマークの発生などに由来する溶接欠陥の発生を抑制することが実現される。 Specifically, it is necessary to improve weld defect resistance, but lowers the SiO 2 (high viscosity / high oxygen potential component) that increases the amount of weld metal oxygen, and instead reduces the effect of increasing the amount of oxygen and improves the slag viscosity. A large amount of Al 2 O 3 (high viscosity / low oxygen potential component) is added. Low oxygen potential component by properly adjusting the CaO-CaF 2 component balance while preferably suppressing slag fluidity by suppressing an increase in flux melting point due to the addition of a large amount of Al 2 O 3 by adding an appropriate amount of CaF 2 The above-mentioned problem is solved by setting the system at 1500 ° C. and the slag viscosity at 1500 ° C. to 0.1 poise or more and less than 1.00 poise. In addition, it is possible to suppress the occurrence of welding defects resulting from the deterioration of the bead appearance, the undercut, the occurrence of potts marks, and the like.

こうして得られた本発明は、次のとおりである。
(1)質量%で、SiO:5〜20%、MnO:1〜5%、CaO:5〜40%、CaF:40%以下、MgO:1〜10%、Al:30〜45%、TiO:1〜4.5%、BaO:1〜10%を含有し、残部は不純物からなる化学組成を有し、1500℃の溶融スラグ粘度が0.1Poise以上1.00Poise未満であることを特徴とするサブマージアーク溶接用溶融型フラックス。
The present invention thus obtained is as follows.
(1) in mass%, SiO 2: 5~20%, MnO: 1~5%, CaO: 5~40%, CaF 2: 40% or less, MgO: 1~10%, Al 2 O 3: 30~ 45%, TiO 2 : 1 to 4.5%, BaO: 1 to 10%, the balance has a chemical composition consisting of impurities, and the molten slag viscosity at 1500 ° C. is 0.1 Poise or more and less than 1.00 Poise A melt type flux for submerged arc welding characterized by being.

本発明により、溶接金属酸素量低減と耐溶接欠陥性向上という、これまで相反していた問題が同時に解決され、溶接欠陥を防止しつつ溶接金属酸素量を低減することが可能となった。   According to the present invention, the conflicting problems of reducing the amount of weld metal oxygen and improving resistance to weld defects have been solved at the same time, and it has become possible to reduce the amount of weld metal oxygen while preventing weld defects.

以下に本発明に係るサブマージアーク溶接用溶融型フラックスの実施の形態について説明する。なお、本明細書において特段のことわりのない「%」は「質量%」を意味する。   Embodiments of a melt type flux for submerged arc welding according to the present invention will be described below. In the present specification, “%” unless otherwise specified means “mass%”.

1.化学組成
以下に、本実施の形態に係るサブマージアーク溶接用溶融型フラックスの化学組成について説明する。
1. Chemical composition The chemical composition of the molten flux for submerged arc welding according to the present embodiment will be described below.

(1)SiO:5〜20%
SiOはスラグを構成する重要な成分である。SiOはスラグをガラス化させ、ビード外観を改善する。またSiOの配合量が少ないとアンダーカットやスラグ巻き込み等の溶接欠陥を生じやすくなる。このため5%以上のSiO配合が必要である。一方でSiOは溶融スラグの酸素ポテンシャルを高くする成分でありSiO量の増加は溶接金属酸素量を増加させるため、上限を20%とする。溶接欠陥の抑制と溶接金属酸素量の低減とを安定して両立させる観点からは、SiOの配合量を7〜15%とすることが好ましい。
(1) SiO 2: 5~20%
SiO 2 is an important component constituting slag. SiO 2 vitrifies the slag and improves the bead appearance. The likely cause welding defects such as inclusion undercut and slag and the amount of SiO 2 is small. For this reason, 5% or more of SiO 2 is necessary. On the other hand, SiO 2 is a component that increases the oxygen potential of the molten slag, and an increase in the amount of SiO 2 increases the amount of weld metal oxygen, so the upper limit is made 20%. From the viewpoint of stably suppressing welding defects and reducing the amount of weld metal oxygen, it is preferable that the blending amount of SiO 2 is 7 to 15%.

(2)MnO:1〜5%
MnOはスラグの流動性を向上させビード外観を滑らかにする効果を有する。また、溶接金属へのMnの歩留まりを改善する効果も期待される。これらの効果を得るには1%以上の配合が必要である。一方でMnOの多量の配合は溶融スラグの酸素ポテンシャルを高くして溶接金属酸素量を増加させ、ビード外観を損なうため上限を5%とする。特に溶接金属へのMn歩留まり改善と良好なビード外観とを安定して両立させる観点からは、MnOの配合量を3.5〜4.5%とすることが好ましい。
(2) MnO: 1 to 5%
MnO has the effect of improving the fluidity of the slag and smoothing the bead appearance. Moreover, the effect which improves the yield of Mn to a weld metal is also anticipated. In order to obtain these effects, a blending ratio of 1% or more is necessary. On the other hand, a large amount of MnO increases the oxygen potential of the molten slag to increase the amount of weld metal oxygen and impair the bead appearance, so the upper limit is made 5%. In particular, from the viewpoint of stably achieving both improvement in Mn yield on the weld metal and good bead appearance, it is preferable that the blending amount of MnO is 3.5 to 4.5%.

(3)CaO:5〜40%
CaOは溶融スラグの酸素ポテンシャルを低くする成分であり、溶接金属酸素量を低減する効果を有する。この効果を得るには5%以上の配合が必要である。酸素量低減には添加量が多いほど好ましいが、多量の添加はスラグ剥離性劣化、フラックスの耐吸湿性劣化によるポックマークの形成などが生じ溶接性を損なう。よってその上限を40%とする。溶接金属酸素量の低減と良好な溶接性とを安定して両立させる観点からは、CaOの配合量を3〜30%とすることが好ましい。
(3) CaO: 5 to 40%
CaO is a component that lowers the oxygen potential of the molten slag and has the effect of reducing the amount of weld metal oxygen. In order to obtain this effect, 5% or more is necessary. Although a larger amount is preferable for reducing the amount of oxygen, a large amount of addition causes deterioration of slag removability and formation of pock marks due to deterioration of moisture absorption resistance of the flux, thereby impairing weldability. Therefore, the upper limit is made 40%. From the viewpoint of stably achieving both a reduction in the amount of weld metal oxygen and good weldability, the CaO content is preferably 3 to 30%.

(4)CaF:40%以下
CaFはスラグ流動性向上、溶接金属酸素量を低減する効果を有する。しかし、多量に配合するとスラグ粘度の低下による耐溶接欠陥性劣化を生じるため、その配合範囲を40%以下とする。好ましい配合範囲は20〜35%である。なお、CaOに対する比率(CaF/CaO)を1.0〜5.0の範囲にすれば、フラックス融点上昇によるスラグ流動性劣化防止の観点から特に好ましい。
(4) CaF 2 : 40% or less CaF 2 has the effect of improving the slag fluidity and reducing the amount of weld metal oxygen. However, if blended in a large amount, deterioration of weld defect resistance due to a decrease in slag viscosity occurs, so the blending range is made 40% or less. A preferred blending range is 20 to 35%. Incidentally, if ratio of CaO (CaF 2 / CaO) in the range of 1.0 to 5.0, particularly preferred from the viewpoint of preventing slag fluidity deterioration due to flux melting point-elevating.

(5)MgO:1〜10%
MgOは溶融スラグの酸素ポテンシャルを低くする成分であり溶接金属酸素量を低減する効果を有する。この効果を得るためには1%以上の配合が必要である。一方で10%を超えて配合す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溶接性を損なうため、その上限を10%とする。好ましい配合範囲は1〜5%である。
(5) MgO: 1 to 10%
MgO is a component that lowers the oxygen potential of the molten slag and has the effect of reducing the amount of weld metal oxygen. In order to obtain this effect, 1% or more is necessary. On the other hand, if the content exceeds 10%, the melting point of the flux increases, the fluidity of the slag deteriorates and the weldability is impaired, so the upper limit is made 10%. A preferred blending range is 1 to 5%.

(6)Al:30〜45%
AlはSiOと比べて溶融スラグの酸素ポテンシャルを高くしない成分であるため、溶接金属酸素量をあまり増加させることなく粘度を向上させる効果を有する。30%未満の添加ではスラグ粘度低下により耐溶接欠陥性を損なう。一方で、多量の添加は溶接金属酸素量を増加させるため、上限を45%とする。溶接金属酸素量の低減と溶接欠陥の抑制とを安定して両立させる観点からは、Alの配合量を30〜40%とすることが好ましい。
(6) Al 2 O 3: 30~45%
Since Al 2 O 3 is a component that does not increase the oxygen potential of the molten slag as compared with SiO 2, it has the effect of improving the viscosity without increasing the amount of weld metal oxygen. Addition of less than 30% impairs weld defect resistance due to a decrease in slag viscosity. On the other hand, since the addition of a large amount increases the amount of weld metal oxygen, the upper limit is made 45%. From the viewpoint of stably reducing the amount of weld metal oxygen and suppressing welding defects, it is preferable that the blending amount of Al 2 O 3 is 30 to 40%.

(7)TiO:1〜4.5%
TiOは少量の添加でスラグ剥離性を改善するとともに溶接金属へのTiの歩留まりを改善する。この効果を得るためには1%以上の添加が必要である。一方で多量の添加は溶融スラグの酸素ポテンシャルを高くして溶接金属酸素量を増加させるため、上限を4.5%とする。好ましい配合範囲は2〜4%である。
(7) TiO 2: 1~4.5%
TiO 2 can be added in a small amount to improve slag peelability and improve the yield of Ti to the weld metal. In order to obtain this effect, addition of 1% or more is necessary. On the other hand, the addition of a large amount increases the oxygen potential of the molten slag and increases the amount of weld metal oxygen, so the upper limit is made 4.5%. A preferable blending range is 2 to 4%.

(8)BaO:1〜10%
BaOはフラックスの融点を調整するとともに、溶融スラグの酸素ポテンシャルを低くして溶接金属酸素量を低減する効果を有する。この効果を得るために1%以上の添加を行う。一方で過剰の添加はビード形状を悪化させるため、その上限を10%とする。好ましい配合範囲は1〜5%である。
(8) BaO: 1-10%
BaO has the effect of adjusting the melting point of the flux and lowering the oxygen potential of the molten slag to reduce the amount of weld metal oxygen. In order to obtain this effect, 1% or more is added. On the other hand, excessive addition deteriorates the bead shape, so the upper limit is made 10%. A preferred blending range is 1 to 5%.

上記の必須成分の他に、溶融型フラックス作製時に不可避的に不純物としてFeO、B等が混入している。これらの成分の混入については、FeOで2.0%以下、Bで1.0%以下であれば、溶接金属酸素量および耐溶接欠陥性に影響しない。 In addition to the above essential components, FeO, B 2 O 3 and the like are inevitably mixed as impurities during the preparation of the molten flux. Regarding the mixing of these components, if the FeO content is 2.0% or less and the B 2 O 3 content is 1.0% or less, the amount of weld metal oxygen and weld defect resistance are not affected.

2.1500℃におけるスラグ粘度
本実施の形態に係るサブマージアーク溶接用溶融型フラックスは、1500℃におけるスラグ粘度が、0.1Poise〜1.00Poiseの範囲にある。
2. Slag Viscosity at 1500 ° C. The molten flux for submerged arc welding according to the present embodiment has a slag viscosity at 1500 ° C. in the range of 0.1 Poise to 1.00 Poise.

スラグ粘度は溶接金属酸素量および耐溶接欠陥性の双方に影響する物性である。スラグ粘度が低すぎると溶接中アーク圧力により溶融池が乱れ、溶接欠陥を生じる。一方でスラグ粘度が高すぎると、スラグ流動性が低下して溶融スラグ・溶融金属間の攪拌力が弱くなる。このため、スラグメタル間の酸素分配平衡における酸素の物質移動速度が低下し溶接金属酸素量は増加する。よって粘度範囲を0.1Poise〜1.00Poiseとする。溶接金属酸素量の低減と良好な溶接性とを安定して両立させる観点からは、好ましい粘度範囲は0.3Poise〜0.8Poiseであり、0.45Poise〜0.65Poiseとすればさらに好ましい。このように、粘度範囲はスラグメタル間の酸素の移動速度を維持する観点で設定されているため、従来のようにフラックス、例えば特許文献5に開示されるフラックスのように溶接欠陥防止の観点で設定される粘度範囲に比べると低めである。   Slag viscosity is a physical property that affects both the weld metal oxygen content and the weld defect resistance. If the slag viscosity is too low, the weld pool is disturbed by the arc pressure during welding, resulting in weld defects. On the other hand, if the slag viscosity is too high, the slag fluidity is lowered and the stirring force between the molten slag and the molten metal becomes weak. For this reason, the mass transfer rate of oxygen in the oxygen distribution equilibrium between slag metals decreases, and the amount of weld metal oxygen increases. Therefore, the viscosity range is 0.1 Poise to 1.00 Poise. From the standpoint of stably achieving both a reduction in the amount of weld metal oxygen and good weldability, the preferred viscosity range is 0.3 poise to 0.8 poise, more preferably 0.45 poise to 0.65 poise. Thus, since the viscosity range is set from the viewpoint of maintaining the movement speed of oxygen between the slag metals, the flux as in the prior art, for example, from the viewpoint of preventing welding defects like the flux disclosed in Patent Document 5 is used. It is lower than the set viscosity range.

なお、この粘度の制御はフラックス成分の調整によって行えばよく、このために調整される成分は特に制限されない。ただし、上記のように本発明に係るフラックスは高温粘度が比較的低く、その一方で粘度を高めるAlを比較的多く含有するため、粘度を低下させる成分の含有量を上記範囲内にて優先的に配合することが好ましい。 The viscosity may be controlled by adjusting the flux component, and the component adjusted for this purpose is not particularly limited. However, as described above, the high temperature viscosity of the flux according to the present invention is relatively low, and on the other hand, since it contains a relatively large amount of Al 2 O 3 that increases the viscosity, the content of the component that decreases the viscosity is within the above range. Therefore, it is preferable to blend them preferentially.

原材料の配合比率を変えることにより、表1に示す化学成分を有するフラックスを試作した。   By changing the mixing ratio of the raw materials, a flux having the chemical components shown in Table 1 was prototyped.

Figure 0005146998
溶接における母材としては、表2の化学成分を示す市販材SM400Bを用いた。母材の板厚は16mmであり、ビードオンプレート溶接で溶接長0.6mの1層溶接を行った。溶接には表3の化学成分を示す直径4mmのソリッドワイヤを用いて、表4に示す条件で単電極サブマージアーク溶接(使用装置:大阪電気製 形式(型式):G1-B3-CG)を実施した。
Figure 0005146998
As a base material in welding, a commercially available material SM400B showing chemical components in Table 2 was used. The thickness of the base material was 16 mm, and single layer welding with a weld length of 0.6 m was performed by bead-on-plate welding. For welding, solid electrode with a diameter of 4 mm indicating the chemical composition shown in Table 3 was used, and single electrode submerged arc welding was performed under the conditions shown in Table 4 (Applicable equipment: Osaka Denki model (model): G1-B3-CG). did.

Figure 0005146998
Figure 0005146998

Figure 0005146998
Figure 0005146998

Figure 0005146998
Figure 0005146998

1500℃スラグ粘度、溶接金属酸素量分析結果、耐溶接欠陥性の結果を表5に示す。また、フラックスと同一組成の溶融スラグを仮定し、スラグメタル熱力学平衡計算により得られたメタル中溶存酸素量計算値も表5に示す。なお、スラグメタル熱力学平衡の計算は汎用の熱力学計算ソフト(例えばFactStage)を用いて行った。   Table 5 shows the results of 1500 ° C slag viscosity, weld metal oxygen content analysis results, and weld defect resistance. Table 5 also shows the calculated amount of dissolved oxygen in the metal obtained by a slag metal thermodynamic equilibrium calculation assuming a molten slag having the same composition as the flux. The slag metal thermodynamic equilibrium was calculated using general-purpose thermodynamic calculation software (for example, FactStage).

ここで、溶接金属酸素量は、作製した溶接ビードを分析することにより求め、300ppm以上の酸素濃度が測定された場合には不適と判断した。また、耐溶接欠陥性については、作製した溶接ビードの健全性を目視検査で確認し、アンダーカットの有無やビード外観状態などを総合的に判断して○(良好)または×(不芳)で示した。   Here, the amount of weld metal oxygen was determined by analyzing the produced weld bead, and was judged to be inappropriate when an oxygen concentration of 300 ppm or more was measured. For weld defect resistance, check the soundness of the weld bead produced by visual inspection, and comprehensively judge the presence or absence of undercut and the appearance of the bead. Indicated.

スラグ粘度は振動片式粘度計を用いてスラグ温度1500℃で測定した。測定装置の概略図を図1に示す。装置は、振動発生器、振動片、レーザー変位計、電気炉および制御用パソコンで構成されている。測定は大気圧雰囲気で行い、振動片とるつぼの材質は白金である。振動発生器は工業用の加振器を用い、正弦発生器と増幅器によって電気的に駆動させる。振動片を加熱により液体状態となった試料内に浸け、振動発生器下方の板バネを中心に振動片を懸垂させ振動片を正弦波振動させる。一定の駆動力で振動させた薄い平板状の振動片を液体中に浸漬させると、液体の粘性抵抗によって振幅が減衰する。振幅の変化は振動片支持棒に固定した鏡の動きをレーザー変位計によって測定する。本測定に用いた粘度計算式は下記式(1)を適用して算出している。   The slag viscosity was measured at a slag temperature of 1500 ° C. using a vibrating piece viscometer. A schematic diagram of the measuring apparatus is shown in FIG. The apparatus is composed of a vibration generator, a vibration piece, a laser displacement meter, an electric furnace, and a control personal computer. The measurement is performed in an atmospheric pressure atmosphere, and the material of the vibrating piece crucible is platinum. The vibration generator uses an industrial vibrator and is electrically driven by a sine generator and an amplifier. The vibrating piece is dipped in a sample that has become a liquid state by heating, and the vibrating piece is suspended around a leaf spring below the vibration generator to vibrate the vibrating piece in a sine wave. When a thin flat plate-like vibrating piece vibrated with a constant driving force is immersed in the liquid, the amplitude is attenuated by the viscous resistance of the liquid. The change in the amplitude is measured by a laser displacement meter with the movement of the mirror fixed to the vibrating bar support rod. The viscosity calculation formula used in this measurement is calculated by applying the following formula (1).

Figure 0005146998
Figure 0005146998

K≡Rm2 / π・fa・A2
ここで、
ρ:試料密度(kg/m3)
μ:液体粘度(Pa・s)
Ea:空気中での振幅(m)
E:試料中の振幅(m
Rm:機械的インピーダンスの抵抗分(kg・m/s)
fa:空気中の共振周波数(Hz)
A:振動片の面積(m2)
K≡Rm 2 / π ・ fa ・ A 2
here,
ρ: Sample density (kg / m 3 )
μ: Liquid viscosity (Pa · s)
Ea: Amplitude in air (m)
E: Amplitude in sample (m
Rm: Mechanical impedance resistance (kg · m / s)
fa: Resonance frequency in air (Hz)
A: Area of vibrating piece (m 2 )

Figure 0005146998
Figure 0005146998

比較例1では、MnO、Al量が本発明範囲から逸脱しているため、ビード外観の劣化による溶接性の低下を生じた。また、フラックス組成は、メタル中溶存酸素量計算値が低く低酸素ポテンシャル成分系であるが、スラグ粘度が本発明範囲を超えているため、溶接金属酸素量を低減できなかった。 In Comparative Example 1, since the amounts of MnO and Al 2 O 3 deviated from the scope of the present invention, weldability was deteriorated due to deterioration of the bead appearance. Moreover, although the flux composition has a low calculated value of dissolved oxygen in the metal and a low oxygen potential component system, the weld metal oxygen content could not be reduced because the slag viscosity exceeded the range of the present invention.

比較例2では、Al量、スラグ粘度が本発明範囲の下限を満たさず、スラグ粘度不足によりアンダーカットが生じて溶接性が低下した。 In Comparative Example 2, the amount of Al 2 O 3 and the slag viscosity did not satisfy the lower limit of the range of the present invention, and undercut occurred due to insufficient slag viscosity, resulting in poor weldability.

比較例3では、SiO量が本発明範囲の上限を超えているため、溶接金属酸素量低減できなかった。 In Comparative Example 3, the amount of weld metal oxygen could not be reduced because the amount of SiO 2 exceeded the upper limit of the range of the present invention.

比較例4では、MnO量が本発明範囲を超えているため、溶接金属酸素量低減できなかった。   In Comparative Example 4, since the amount of MnO exceeded the range of the present invention, the amount of weld metal oxygen could not be reduced.

比較例5では、溶接金属酸素量を低減できたものの、CaO量が本発明範囲を超えているため、ビード表面にポックマークが生じビードの健全性を損ない、溶接性の低下を生じた。   In Comparative Example 5, although the amount of weld metal oxygen could be reduced, since the CaO amount exceeded the range of the present invention, a pock mark was generated on the bead surface, and the soundness of the bead was impaired, resulting in a decrease in weldability.

比較例6では、TiO量が本発明範囲の上限を満たしていないためスラグ流動性が悪くなり、ポックマークが生じビードの健全性を損ない、溶接性の低下を生じた。 In Comparative Example 6, since the amount of TiO 2 did not satisfy the upper limit of the range of the present invention, the slag fluidity deteriorated, pock marks were generated, the bead soundness was impaired, and weldability was deteriorated.

比較例7では、MnO、TiO、BaO量が本発明範囲から逸脱しているため、ビード外観の劣化による溶接性低下を生じた。 In Comparative Example 7, since the amounts of MnO, TiO 2 and BaO deviated from the scope of the present invention, weldability was deteriorated due to deterioration of the bead appearance.

比較例8では、Al量が本発明範囲を超えているため、溶接金属酸素量を十分に低減できなかった。 In Comparative Example 8, the amount of weld metal oxygen could not be reduced sufficiently because the amount of Al 2 O 3 exceeded the range of the present invention.

比較例9では、CaF量が本発明範囲の上限を超えているため、スラグ粘度が本発明範囲の下限を満たすことができなかった。このため、スラグ粘度不足によりアンダーカットが生じて溶接性が低下した。 In Comparative Example 9, since the amount of CaF 2 exceeded the upper limit of the present invention range, the slag viscosity could not satisfy the lower limit of the present invention range. For this reason, undercut occurred due to insufficient slag viscosity, and weldability deteriorated.

比較例10では、フラックス組成はメタル中溶存酸素量計算値が低く低酸素ポテンシャル成分系であり、フラックス組成も本発明範囲であるが、1500℃スラグ粘度が本発明範囲を超えているため、溶接金属酸素量を低減できなかった。   In Comparative Example 10, the flux composition is a low oxygen potential component system with a low calculated amount of dissolved oxygen in the metal, and the flux composition is also within the scope of the present invention, but since the 1500 ° C. slag viscosity exceeds the scope of the present invention, welding is performed. The amount of metal oxygen could not be reduced.

上記比較例に対して、本発明例11から15に示したように本発明範囲に配合比、スラグ粘度を制御した溶融型フラックスでは溶接金属酸素量を低減すると同時に耐溶接欠陥性向上も実現した。   Compared to the above comparative example, as shown in Invention Examples 11 to 15, in the melt type flux in which the blending ratio and slag viscosity are controlled within the scope of the present invention, the amount of weld metal oxygen was reduced and at the same time improved weld defect resistance was realized. .

スラグ粘度の測定に用いた振動片式粘度計の概略図である。It is the schematic of the vibrating piece type viscometer used for the measurement of slag viscosity.

Claims (1)

質量%で、SiO:5〜20%、MnO:1〜5%、CaO:5〜40%、CaF:40%以下、MgO:1〜10%、Al:30〜45%、TiO:1〜4.5%、BaO:1〜10%を含有し、残部は不純物からなる化学組成を有し、1500℃の溶融スラグ粘度が0.1Poise以上1.00Poise未満であることを特徴とするサブマージアーク溶接用溶融型フラックス。 By mass%, SiO 2: 5~20%, MnO: 1~5%, CaO: 5~40%, CaF 2: 40% or less, MgO: 1~10%, Al 2 O 3: 30~45%, TiO 2 : 1 to 4.5%, BaO: 1 to 10%, the balance has a chemical composition consisting of impurities, and the molten slag viscosity at 1500 ° C. is not less than 0.1 poise and less than 1.00 poise. Characteristic fusion flux for submerged arc welding.
JP2007316223A 2007-12-06 2007-12-06 Fused flux for submerged arc welding Expired - Fee Related JP5146998B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2007316223A JP5146998B2 (en) 2007-12-06 2007-12-06 Fused flux for submerged arc welding

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2007316223A JP5146998B2 (en) 2007-12-06 2007-12-06 Fused flux for submerged arc welding

Publications (2)

Publication Number Publication Date
JP2009136898A JP2009136898A (en) 2009-06-25
JP5146998B2 true JP5146998B2 (en) 2013-02-20

Family

ID=40868092

Family Applications (1)

Application Number Title Priority Date Filing Date
JP2007316223A Expired - Fee Related JP5146998B2 (en) 2007-12-06 2007-12-06 Fused flux for submerged arc welding

Country Status (1)

Country Link
JP (1) JP5146998B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5869023B2 (en) * 2013-04-04 2016-02-24 Jfeスチール株式会社 Fused flux for submerged arc welding

Also Published As

Publication number Publication date
JP2009136898A (en) 2009-06-25

Similar Documents

Publication Publication Date Title
JP5334725B2 (en) Sintered flux for 9% Ni steel submerged arc welding
JP5438663B2 (en) Flux cored wire
JP5111028B2 (en) Flux-cored wire for gas shielded arc welding
JP4903622B2 (en) Mold powder for continuous casting of steel and continuous casting method
US10112267B2 (en) Flux-cored wire for Ar—CO2 mixed gas shielded arc welding
JP2016137508A (en) Flux-cored wire for carbon dioxide gas shielded arc welding
KR102675635B1 (en) Flux Cored Wire and Welding Methods
JP2012115878A (en) Flux-cored wire
JPH08267282A (en) Flux-cored wire for austenitic stainless steel
JP5146998B2 (en) Fused flux for submerged arc welding
SE425891C (en) COATED ELECTROD BEFORE BAKING WELDING
JP4486878B2 (en) Mold powder for continuous casting of steel and continuous casting method
CA2024498C (en) Gas metal arc welding wire
RU2074800C1 (en) Flux for welding and surfacing
KR102864409B1 (en) Flux for submerged arc welding
KR101662373B1 (en) Flux cored wire for gas shielded arc welding, and gas shielded arc welding method
JP5869023B2 (en) Fused flux for submerged arc welding
JP6787043B2 (en) Flux for submerged arc welding
JP4581842B2 (en) Fused flux for submerged arc welding
JP2009291802A (en) Low hydrogen covered electrode for welder using dc power source
JP2022146842A (en) Fusion type flux for fillet submerged arc welding
KR100364873B1 (en) Agglomerated flux for submerged arc welding
JP2001219274A (en) Tic welding method
JP7787658B2 (en) Fusible flux for submerged arc welding
JP2023176305A (en) Ingot manufacturing method

Legal Events

Date Code Title Description
A621 Written request for application examination

Free format text: JAPANESE INTERMEDIATE CODE: A621

Effective date: 20100223

A521 Request for written amendment filed

Free format text: JAPANESE INTERMEDIATE CODE: A523

Effective date: 20121011

A711 Notification of change in applicant

Free format text: JAPANESE INTERMEDIATE CODE: A712

Effective date: 20121011

TRDD Decision of grant or rejection written
A01 Written decision to grant a patent or to grant a registration (utility model)

Free format text: JAPANESE INTERMEDIATE CODE: A01

Effective date: 20121023

A61 First payment of annual fees (during grant procedure)

Free format text: JAPANESE INTERMEDIATE CODE: A61

Effective date: 20121121

R150 Certificate of patent or registration of utility model

Ref document number: 5146998

Country of ref document: JP

Free format text: JAPANESE INTERMEDIATE CODE: R150

Free format text: JAPANESE INTERMEDIATE CODE: R150

FPAY Renewal fee payment (event date is renewal date of database)

Free format text: PAYMENT UNTIL: 20151207

Year of fee payment: 3

S533 Written request for registration of change of name

Free format text: JAPANESE INTERMEDIATE CODE: R313533

R350 Written notification of registration of transfer

Free format text: JAPANESE INTERMEDIATE CODE: R350

LAPS Cancellation because of no payment of annual fees