JPS589795A - Flux for submerged arc welding by belt-like electrode - Google Patents

Flux for submerged arc welding by belt-like electrode

Info

Publication number
JPS589795A
JPS589795A JP10711081A JP10711081A JPS589795A JP S589795 A JPS589795 A JP S589795A JP 10711081 A JP10711081 A JP 10711081A JP 10711081 A JP10711081 A JP 10711081A JP S589795 A JPS589795 A JP S589795A
Authority
JP
Japan
Prior art keywords
less
agent
welding
flux
alloying
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.)
Pending
Application number
JP10711081A
Other languages
Japanese (ja)
Inventor
Motoi Tokura
戸倉 基
Hiroyuki Koike
弘之 小池
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 JP10711081A priority Critical patent/JPS589795A/en
Publication of JPS589795A publication Critical patent/JPS589795A/en
Pending legal-status Critical Current

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B23MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
    • B23KSOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
    • B23K35/00Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
    • B23K35/22Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
    • B23K35/36Selection of non-metallic compositions, e.g. coatings, fluxes; Selection of soldering or welding materials, conjoint with selection of non-metallic compositions, both selections being of interest
    • B23K35/362Selection of compositions of fluxes

Landscapes

  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Nonmetallic Welding Materials (AREA)

Abstract

PURPOSE:To provide a flux for welding by which build-up layers of high toughness and high strength are easily obtained by slag making agents contg. specific amts. of CaO, CaF2, etc., by deoxygenizing agents for alloying agents contg. specific amts. of C, Si, Mn, etc.. CONSTITUTION:The flux contg. 5-25% CaO or CaCO3, 3-30% CaF2, 2-30% Al2O3, 3-30% MgO, 5-25% SiO2 as slag making agents, contg. <=0.5% C., 0.2- 3.0% Si, 1.9-11.5% Mn, 0.4-4.5% Ni, 1.3-10.2% Cr, <=40% iron as deoxygenizing agents for alloying and consisting of the balance unavoidable impurities is prepd. If necessary, it is possible to contain >=1 kind of <=3.6% Mo, <=5.7% V as alloying agents and further 1 or 2 kinds of <=15% TiO2 or ZrO2 as other components of the slag making agents.

Description

【発明の詳細な説明】 本発明は、高温靭性のすぐれた肉盛層を得るための帯状
電極サブマージアーク溶接に適するフラックスに関する
ものであり、特に高硬度肉盛層に使用中発生した割れ、
熱亀裂などが母材に急速に伝播することを防止するため
の高温靭性にすぐれた下盛層を得るための帯状電極サブ
マージアーク溶接用フラックスを提供することを目的と
している。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a flux suitable for band-shaped electrode submerged arc welding to obtain a build-up layer with excellent high-temperature toughness.
The object of the present invention is to provide a flux for submerged arc welding with a band-shaped electrode to obtain an underlay layer with excellent high-temperature toughness to prevent thermal cracks from rapidly propagating to the base metal.

従来より製鉄所における各種ロール、ローラ類、例えば
連続鋳造用ピンチロール、熱延ワークロール、テーブル
ローラ、冷延ワークロール、バックアップロール、連続
酸洗ピンチロールなどには肉盛溶接法による再生修理し
たものが使用され耐用期間の向上に貢献している。
Traditionally, various rolls and rollers used in steel mills, such as pinch rolls for continuous casting, hot rolling work rolls, table rollers, cold rolling work rolls, backup rolls, and continuous pickling pinch rolls, have been refurbished and repaired using the overlay welding method. This contributes to increasing the lifespan of products used.

しかし、これらの^盛施工の場合、直接耐摩耗性を要求
される上盛層を得るための溶接材料及び溶接法について
は数多く研究がなされており、それなりの成果が得られ
ているが、耐用期間向上を目的としだ下盛層を得るため
の溶接材料及び溶接法については、あまり研究がなσれ
てぃないのが現状である。
However, in the case of these overlay constructions, many studies have been conducted on welding materials and welding methods to obtain the overlay layer that requires direct wear resistance, and although some results have been obtained, At present, not much research has been conducted on welding materials and welding methods for obtaining a welding layer for the purpose of improving the welding period.

例えば肉盛層がうすくでも良い場合は、下盛をせず直接
上盛材で肉盛溶接したり、又厚い肉盛層を必要とする場
合、いわゆるビルドアップ材である軟鋼溶接材で下盛し
た後、肉盛溶接するなどの手段がとられている。
For example, if a thin build-up layer is acceptable, welding can be performed directly with overlay material without using the underlay, or if a thick overlay is required, underlay welding can be done with a mild steel welding material, which is a so-called build-up material. After that, measures such as overlay welding are taken.

この伯母材の炭素当量が高い場合、直接母材上へ上盛材
を肉盛すると母材からの炭素の移行により肉盛層に割れ
が発生するのを防止するため、低炭素軟鋼材あるいはオ
ーステナイト系ステンレス鋼材で下盛するなどの手段が
用いられている。
If the carbon equivalent of this base metal is high, if the overlay material is overlaid directly on the base metal, it is necessary to use low carbon mild steel or austenite to prevent cracks from occurring in the overlay layer due to carbon migration from the base metal. Measures such as underlaying with stainless steel materials are used.

このような下盛付選択の基準となるのは、溶接材料のコ
スト及び割れ発生防止の2点であり、耐用期間の延長を
はかるためには、上盛材の耐摩耗、耐割れ性等を改善す
ることに主力がおかれてぃた。
The criteria for selecting such underlayment are the cost of the welding material and the prevention of cracking.In order to extend the service life, the wear resistance, cracking resistance, etc. of the overlay material should be checked. The main focus was on improvement.

しかしながら、近年の飛躍的な生産性向上のすう勢の中
で、操業条件は一層苛酷となり、根本的に肉盛技術全般
を見直す必要が生じて来た。 ゛このような実情に!!
み、−例を連鋳ピンチロールにとり、耐用期間の長短を
決定する因子について検討した結果、表面から順次摩耗
していく場合は上盛層の硬さが大きな因子であること、
使用中発生する割れ、熱亀裂による廃却、折損の場合は
割れ、熱亀裂発生に及ぼす因子としては、上盛材の耐割
れ性、耐熱亀裂性が挙げられるが、これが大きく成長し
ていく段階になると、下盛材あるいは母材の靭性が大き
な要因となり、下盛材あるいは母材の靭性が高い場合に
は、割れは深く伝播せず、上盛材が全面摩耗するまで実
用に供しうろことが判明した。
However, with the trend of dramatic productivity improvement in recent years, operating conditions have become even more severe, and it has become necessary to fundamentally review the overlay technology in general.゛This is the reality! !
Taking the continuous casting pinch roll as an example, we investigated the factors that determine the length of the service life, and found that the hardness of the overlay layer is a major factor in the case of gradual wear starting from the surface.
Cracks that occur during use, scrapping due to thermal cracks, cracks in the case of breakage, and factors that affect the occurrence of thermal cracks include the cracking resistance of the overlay material and the heat cracking resistance, but this is the stage at which it grows significantly. In this case, the toughness of the underlayment material or base material is a major factor.If the underlayment material or base material has high toughness, the crack will not propagate deeply and the scales will not be used until the overlayment material is completely worn out. There was found.

その反面最悪の状態である折損事故は、下盛材あるいは
母材の靭性低下が主な原因であることも判明した。尚、
軟鋼材で下盛した場合についてみると、靭性はある程度
のレベルを保つが強度が上盛層、母材にくらべてはるか
に低いため割れ、熱亀裂の応力に抗しきれずに破断する
場合の多いことが分った。
On the other hand, it was also found that the worst case, the breakage accident, was mainly caused by a decrease in the toughness of the underlay material or the base material. still,
When we look at the case of underlaying with mild steel, the toughness is maintained at a certain level, but the strength is much lower than that of the overlaying layer and the base material, so it often cracks and breaks without being able to withstand the stress of thermal cracking. I found out.

本発明者らは強度を高いレベルに保ちながら、なおかつ
靭性を高くすればよいことを見出し、造滓剤成分の検討
及び合金成分系の検討を行なった結果、本発明を完成し
たものである。
The present inventors discovered that it is sufficient to increase toughness while maintaining strength at a high level, and as a result of studying slag forming agent components and alloy component systems, the present invention was completed.

すなわち本発明の要旨は、造滓剤としてCaO又はCa
C0,5〜25%、CaF25〜25%、A12032
〜30%、Mg03〜30%、SiO□5〜25%また
合金剤、脱酸剤としてC015%以下、SiO,2〜3
.0%、Mn 1.9〜] 1.5%、NiO,4〜4
.5%、Cr 1.3〜10.2%、鉄分40%以下を
含み、残部は不可避不純物よりなり、又はこれに合金剤
として3.6%以下のMo2S、7%以下のVの1種以
上を含み、又はこれに更に造滓剤の他の成分として15
%以下の’l’i02もしくは、ZrO2の1種又は2
種を含む帯状電極サブマージアーク゛溶接用フラックス
にある。
That is, the gist of the present invention is to use CaO or Ca as a slag forming agent.
C0.5-25%, CaF25-25%, A12032
~30%, Mg03~30%, SiO□5~25% Also as alloying agent and deoxidizing agent CO15% or less, SiO,2~3
.. 0%, Mn 1.9~] 1.5%, NiO, 4~4
.. 5%, Cr 1.3 to 10.2%, iron content 40% or less, the remainder consisting of unavoidable impurities, or one or more of the following as an alloying agent: 3.6% or less Mo2S, 7% or less V or further contains 15 as other components of the slag-forming agent.
% or less of 'l'i02 or one or two of ZrO2
A strip-shaped electrode containing seeds is used for submerged arc welding flux.

以下に本発明の詳細な説明する。The present invention will be explained in detail below.

先ず(:aCO3は、溶接アークによる熱分解により発
生するCOtガスの還元性雰囲気をもって大気よりアー
クを遮蔽するのに有効に作用するとともに、その分解生
成物であるCaOは強塩基性のスラグを゛形成し、精錬
作用が期待される。この場合、サブマージアーク溶接で
あるので、アーク周辺はフラックスで覆われており、必
らずしも強力なCO2ガスによる雰囲気の保護を必要と
せず、むしろCaOによるスラグ精錬作用への効果が必
要となる。
First of all, (aCO3) acts effectively to shield the arc from the atmosphere with the reducing atmosphere of COt gas generated by thermal decomposition by the welding arc, and its decomposition product CaO protects against strongly basic slag. In this case, since it is submerged arc welding, the area around the arc is covered with flux, and the atmosphere does not necessarily need to be protected by strong CO2 gas, but rather CaO It is necessary to have an effect on the slag refining action.

CaO又はCaCO3が5%未満では精錬作用が期待で
きず合金の歩留も低くなる。又、25%超の場合は、ス
ラグ自体が過剰に塩基性となりすぎスラグの粘性が増大
しすぎ、溶接作業性を損なうのでその配合量は5〜25
%に限定゛されるべきである。
If CaO or CaCO3 is less than 5%, no refining action can be expected and the yield of the alloy will be low. In addition, if it exceeds 25%, the slag itself becomes too basic and the viscosity of the slag increases too much, impairing welding workability, so the blending amount should be 5 to 25%.
%.

CaF2は5%以以上台することによりスラグの融点を
下げ、スラグの流動性を適度に保つのに有効であるが、
25%超の配合は、アークも不安定になりがちであるの
で5〜25%の範囲に限定した。
CaF2 is effective in lowering the melting point of slag and maintaining appropriate fluidity of slag by setting it at 5% or more.
If the content exceeds 25%, the arc tends to become unstable, so the content was limited to a range of 5 to 25%.

Al2O5は2%以以上台することによりスラグ形状が
安定し、肉盛溶接した場合、母材と溶接金属とのぬれ角
度が小さくなり、なじみがよくなりアンダーカットの防
止に効果があるが、多量に配合すると、スラグの融点が
上昇し、流動性が減じアークの不安定化を招くことにな
るので、30%以下とした。
When the Al2O5 content is 2% or more, the slag shape becomes stable, and when overlay welding, the wetting angle between the base metal and the weld metal becomes smaller, which improves familiarity and is effective in preventing undercuts. If it is added to the slag, the melting point of the slag will increase, the fluidity will decrease, and the arc will become unstable, so the content was set at 30% or less.

MgOは3%以上の配合によりアークの安定化とスラグ
の剥離性の向上、アンダーカットの防止に寄与しうるが
、30%超の配合はビード形状が乱れる原因となるので
、3〜30%の範囲とすべきである。
MgO in a proportion of 3% or more can contribute to stabilizing the arc, improving slag releasability, and preventing undercuts, but a proportion of more than 30% may cause the bead shape to be disordered, so MgO in a proportion of 3 to 30% should be within the range.

S i02は5%以以上台することによりスラグの流動
性が良好になり、安定した溶接ができるが、25%を超
えた配合では溶接金属中へStが過剰に含まれるので好
ましくない。
When the SiO2 content is 5% or more, the fluidity of the slag becomes good and stable welding is possible, but when the Si02 content exceeds 25%, excessive St is included in the weld metal, which is not preferable.

更に、上記造滓剤にTt02 +  ZrO2の1種以
上を、スラグの流動性を良好に保ちピード幅を拡げ、ア
ークの安定性、を良好に保つ目的で添加することができ
、これにより溶融プールの安定化などに効果がある。し
かし15%を超えると、逆にスラグの流動性が大となり
すぎスラグが先行する結果、ビード形状が乱れる傾向が
あるので15%以下とする必要がある。
Furthermore, one or more of Tt02 + ZrO2 can be added to the above-mentioned slag forming agent in order to maintain good fluidity of the slag, widen the peed width, and maintain good arc stability. It is effective in stabilizing the However, if it exceeds 15%, the fluidity of the slag becomes too high, and as a result, the slag tends to move forward, causing the bead shape to become disordered, so it is necessary to keep it below 15%.

次に本発明において用いられる合金剤、脱酸剤について
述べると、まずCは少量の添加で溶接金属強度を増すの
に有効な元素であるが、過度に含有されると靭性な低下
させる原因となり、肉盛溶接の如き母材が中高炭素鋼で
ある場合が多いことを想定すると、0.5%以下に押え
る必要がある。
Next, talking about the alloying agent and deoxidizing agent used in the present invention, first of all, C is an effective element for increasing the strength of weld metal when added in small amounts, but when contained in an excessive amount, it can cause a decrease in toughness. Assuming that the base material for overlay welding is often medium-high carbon steel, it is necessary to suppress the content to 0.5% or less.

なお、Cは鋳鉄粉、クロム力−ノくイドやCを含む合金
剤、例えばFe−Mn + Fe−8t + Fe−M
o + Fe−Crなどの形で添加される。
Note that C is cast iron powder, chromium oxide, or an alloying agent containing C, such as Fe-Mn + Fe-8t + Fe-M
It is added in the form of o + Fe-Cr, etc.

Stは通常の帯状電極サブマージアーク溶接では、脱酸
のため0.2%は必要であるが、3.0%超になると溶
接金属の靭性の低下をきたしやすい傾向があるので、0
,2〜3.0%の範囲とすべきである。なお、SIはF
e−8t + 51−Mn +金属Siなどの形で添加
することが可能である。
In normal strip electrode submerged arc welding, 0.2% of St is necessary for deoxidation, but if it exceeds 3.0%, it tends to reduce the toughness of the weld metal, so it should be 0.
, 2-3.0%. In addition, SI is F
It is possible to add in the form of e-8t + 51-Mn + metal Si.

Mnについても通常の鋼に含有している程度の量を脱酸
のために必要とし、フラックスから添加する場合最低で
も1.9%を必要とするが、11.5%超の添加によっ
ても溶接金属の機械的性質等の顕著な改善はみられない
ので、その含有量を1.9〜11.5%に限定した。な
おMnはFe −Mn + St −Mnなどの形で添
加することが可能である。
Regarding Mn, an amount similar to that contained in ordinary steel is required for deoxidation, and when added from flux, a minimum of 1.9% is required, but even if more than 11.5% is added, welding Since no significant improvement was observed in the mechanical properties of the metal, the content was limited to 1.9 to 11.5%. Note that Mn can be added in a form such as Fe-Mn+St-Mn.

Niは溶接金属の靭性を改善し、衝撃値を向上させる元
素であるが、過剰に添加するとかえって衝撃値が低下す
る。
Ni is an element that improves the toughness and impact value of weld metal, but when added in excess, the impact value decreases.

第1図は造滓剤としてCaCO37%、CaF220 
%、AI!20s 25%、Mg016%、5i022
0%、脱酸前11、合金剤として、CO,1%、Mn 
5 %、Cr 6 %を基本成分として、これにNi添
加量を種々変えて、軟鋼帯状電極(o、4txso闘幅
、0.06%C,0,29%Mn)を組合せて、溶接条
件900A、24V、18cm/mix 、予熱パス間
温度150〜200℃で6層盛した溶接金属から採取し
た衝撃試験片について高温衝撃試験を行ない、試験温度
200℃における衝撃値の変化をみたものである。
Figure 1 shows CaCO37% and CaF220 as slag forming agents.
%, AI! 20s 25%, Mg016%, 5i022
0%, before deoxidation 11, as alloying agent, CO, 1%, Mn
The basic components were 5% Cr and 6% Cr, and various Ni addition amounts were used in combination with a mild steel strip electrode (O, 4TxSO fighting width, 0.06%C, 0.29%Mn), and welding conditions were 900A. , 24V, 18cm/mix, and a preheating pass temperature of 150 to 200°C. A high-temperature impact test was conducted on an impact test piece taken from a six-layer weld metal, and the change in impact value at a test temperature of 200°C was observed.

図から明らかなようにN1の添加は溶接金属の衝撃値の
向上に寄与し、0.4%以上のNi添加により良好な値
を示すが、4.5%超のNi添加量になると、かえって
衝撃値は低くなるのでNi含有量は04〜4,5%の範
囲に限定した。なお、Niは金属Ni + Fe−Ni
などの形で添加しうる。
As is clear from the figure, the addition of N1 contributes to improving the impact value of the weld metal, and a good value is shown with the addition of 0.4% or more Ni, but when the amount of Ni added exceeds 4.5%, the impact value of the weld metal increases. Since the impact value is low, the Ni content is limited to a range of 0.4 to 4.5%. Note that Ni is metal Ni + Fe-Ni
It can be added in the form of

Crは溶接金属の強度を上げるのに必要な元素であり、
強度向上のためには、1.3%以上の添加が必要である
が、一方衝撃値についてみると、過剰のCr添加は好ま
しいものではない。
Cr is an element necessary to increase the strength of weld metal,
In order to improve the strength, it is necessary to add 1.3% or more of Cr, but on the other hand, in terms of impact value, excessive addition of Cr is not preferable.

第2.図は造滓剤としてCaCO37%、CaF220
%。
Second. The figure shows CaCO37% and CaF220 as sludge forming agents.
%.

U2os 25%、MgO16%、5i0220%、脱
酸剤、合金剤として、C011%、Mn 5%、Ni2
.5%を基本成分として、これにCr添加量を種々変え
て、軟鋼帯状電極(0,4tX50朋幅、0.06%C
,0,29%Mn)を組合せて溶接条件900A、 2
4V、 18(In/順、予熱パス間温度150〜20
0℃で6層盛した溶接金属から採取した衝撃試験片につ
いて高温衝撃試験を行ない試験温度200℃における衝
撃値の変化をみたものである。
U2os 25%, MgO 16%, 5i020%, deoxidizer, alloying agent, C011%, Mn 5%, Ni2
.. Using 5% as the basic component, and varying the amount of Cr added, mild steel strip electrodes (0.4t x 50mm width, 0.06%C
, 0.29%Mn), welding conditions 900A, 2
4V, 18 (In/order, preheating pass temperature 150~20
A high-temperature impact test was conducted on an impact test piece taken from a weld metal deposited in six layers at 0°C, and changes in impact value at a test temperature of 200°C were observed.

図から明らかなように、Crの添加により衝撃値は漸次
低下の傾向を示すが、Cr含有量が、]0,2%までは
その低下傾向はゆるやかであり高い水準を保っているが
、102%超となると急激に低下するので、Crの範囲
は1.3〜10.2%とした。
As is clear from the figure, the impact value shows a tendency to gradually decrease with the addition of Cr, but when the Cr content reaches ]0.2%, the decreasing trend is gradual and remains at a high level. %, the content of Cr decreases rapidly, so the range of Cr was set to 1.3 to 10.2%.

なお、Crは金属Cr r Fe −Cr +クロムカ
ーノ(イドなどの形で添加することが可能である。
Note that Cr can be added in the form of metal Cr r Fe -Cr + chromium carbide.

5.7%以下のVの1種以上を添加することができ、こ
れら元素の添加により、更に溶接金属の衝撃値を低下さ
せずに、強度レベルの向上をはかることができる。なお
、Mo + Vは金属Mo + Fa −Me +金属
V、Fe−Vなどの形で添加することが可能である。
One or more types of V can be added in an amount of 5.7% or less, and by adding these elements, it is possible to improve the strength level without further reducing the impact value of the weld metal. Note that Mo + V can be added in the form of metal Mo + Fa - Me + metal V, Fe-V, or the like.

また、 Si t Mrz Cr+ Mos Vなどを
合金鉄の形で添加する場合、これら合金鉄に含まれる鉄
分がフラックス中の鉄源となることは勿論であるが、そ
の他アークの安定性、ビード外観、母材とのなじみの改
善に効果がある鉄粉自体を単独に添加することも有効で
ある。しかしながら鉄分の合計が40%を超えると、ビ
ード外観の劣化、スラグ剥離性の劣化などが生じ適当で
ないので、適正成分範囲を40%以下と規定した。
In addition, when adding Si t Mrz Cr + Mos V etc. in the form of ferroalloy, the iron contained in these ferroalloys will of course become the iron source in the flux, but it will also affect the stability of the arc, the appearance of the bead, It is also effective to add iron powder alone, which is effective in improving compatibility with the base material. However, if the total iron content exceeds 40%, the bead appearance deteriorates, the slag removability deteriorates, etc., and this is not appropriate, so the appropriate content range is defined as 40% or less.

次に実施例に基いて本発明の効果を更に具体的に説rj
At−る。
Next, the effects of the present invention will be explained in more detail based on examples.
At-ru.

実施例 母材は全試験とも、第1表に示す545Cを使°用し、
第2表に示す条件で溶接を行なった。
The base material used in all tests was 545C shown in Table 1.
Welding was performed under the conditions shown in Table 2.

第1表 第2表 使用した帯状電極を第3表に示した。又、第4、 表に
フラックスを一括して示した。
Table 1 Table 2 Table 3 shows the strip electrodes used. Also, in the fourth table, fluxes are shown all at once.

第3表 第3表の帯状電極と第4表のフラックスを組1せて溶接
した結果を第5表に示す。
Table 3 Table 5 shows the results of welding a combination of the strip electrode shown in Table 3 and the flux shown in Table 4.

比較例として示したフラックスF−8,F−9は造滓剤
成分の配合比率が適正でないため、溶接作業性が悪く、
ビード外観不良、スラグの剥離性が劣化し、多層盛が困
難であるので以後の試験を中断した。
Fluxes F-8 and F-9 shown as comparative examples have poor welding workability because the blending ratio of slag-forming agent components is not appropriate.
The bead appearance was poor, the slag releasability deteriorated, and multilayer deposition was difficult, so subsequent tests were discontinued.

又、フラックスF−10,F−11,F−12は作業性
良好であり、健全な溶接は可能であるが、合金剤、脱酸
剤成分の配合比率が適正でないため溶接金属の衝撃値は
低く実用性があるとは云い難い。
Fluxes F-10, F-11, and F-12 have good workability and enable sound welding, but the impact value of the weld metal is low because the blending ratio of alloying agent and deoxidizing agent components is not appropriate. It is difficult to say that it is low and practical.

F −137ラツクスは溶接作業性も良好で、溶接金属
の衝撃値も高い水準を維持しているが、合金剤、脱酸剤
成分の配合比率が低いため引張強さが低く、これも又実
用性があるとは云い難い。
F-137 Lux has good welding workability and the impact value of the weld metal maintains a high level, but its tensile strength is low due to the low blending ratio of alloying agents and deoxidizing agents, which also makes it difficult to put into practical use. It is hard to say that there is a sex.

これと比較して本発明例では、溶接作業性は良好であり
、又溶接金属の衝撃値、引張強ざとも高い水準を維持で
き、良好な結果を示した。
In comparison, in the examples of the present invention, welding workability was good, and the impact value and tensile strength of the weld metal were able to maintain high levels, showing good results.

以上詳細に説叩したように、本発明フラックスにより高
靭性、高強度肉盛層を容易に得ることができ、その意義
は大きいものがある。
As explained in detail above, high toughness and high strength build-up layers can be easily obtained using the flux of the present invention, which has great significance.

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

第1図はNi含有量と溶接金属の衝撃値との関係を示す
グラフであり、第2図はCr含有量と溶接金属の衝撃値
との関係を示すグラフである。 第2図 53
FIG. 1 is a graph showing the relationship between the Ni content and the impact value of the weld metal, and FIG. 2 is a graph showing the relationship between the Cr content and the impact value of the weld metal. Figure 2 53

Claims (1)

【特許請求の範囲】 1、造滓剤としてCaO又はCaC0,5〜25 %、
CaF25〜25%、A12os 2〜30%、Mg0
3〜30%、5i025〜25%、また合金剤脱酸剤と
して、C0,5%以下、Si0.2〜3.0%、Mn1
.9〜11.5%、Ni0.4〜4.5%、Cr1.3
〜10.2%、鉄分40%以下を含み、残部は不可避不
純物よりなる帯状電極サブマージアーク溶接用フラック
ス。 2、造滓剤としてCaO又はCaCO35〜25 %、
CaF25〜25%、A12os 2〜30%、Mg0
3〜30%、5iOz5〜25%、また合金剤脱酸剤と
して、CO35%以下、8i 0.2〜3.0 %、M
n 1.9〜11.5%、Ni0.4〜4.5%、Cr
 1.3〜10.2%、鉄分40%以下、更に合金剤と
して3.6%以下のMo、5.7%以下のVの1種以上
を含み、残部は不可避不純物よりなる帯状電極サブマー
ジアーク溶接用スラックス。 3、造滓剤としてCaO又はCaC0,5〜25%、C
aF、 5〜25%、A40s 2〜30%、MgO3
〜30%、81025〜25%、また合金剤、脱酸剤と
してC0,5%以下、SiO,2〜3.0%、Mn 1
.9〜11.5%、Ni0.4〜4.5%、Cr 1.
3〜10.2%、鉄分40%以下、更に造滓剤として1
5%以下のTiO2もしくはZrO2の1種又は2種を
含み、残部の不可避不純物よりなる帯状電極サブマージ
アーク溶接用フラックス。 4、造滓剤としてCaO又はCaCO35〜25%、C
aF25〜25%、A12os 2〜30%、Mg03
〜30%、5i025〜25%、また合金剤、脱酸剤と
してSiO,2〜3.0%、Mn 1.9〜11.5%
、NiO,4〜4.5%、Cr 1.3〜10.2%、
鉄分40%以下、更に合金剤としてC015%以下、3
.6%以下のMo、5.7%以下のVの181以上、造
滓剤として15%以下のTie、もしくはZrO2の1
種又は2種を夫々含み、残部は不可避不純物よりなる帯
状電極サブマージアーク溶接用フラツクス。
[Claims] 1. CaO or CaC 0.5 to 25% as a slag forming agent;
CaF25-25%, A12os 2-30%, Mg0
3-30%, 5i025-25%, and as an alloying agent deoxidizer, C0.5% or less, Si0.2-3.0%, Mn1
.. 9-11.5%, Ni0.4-4.5%, Cr1.3
Flux for submerged arc welding with a band-shaped electrode, containing up to 10.2% iron and 40% or less iron, with the remainder consisting of unavoidable impurities. 2. CaO or CaCO35-25% as a slag forming agent,
CaF25-25%, A12os 2-30%, Mg0
3-30%, 5iOz5-25%, and as an alloying agent deoxidizer, CO35% or less, 8i 0.2-3.0%,
n 1.9-11.5%, Ni 0.4-4.5%, Cr
1.3 to 10.2%, iron content of 40% or less, and further contains one or more of the following alloying agents: 3.6% or less of Mo, 5.7% or less of V, and the remainder is unavoidable impurities. Slacks for welding. 3. CaO or CaC0.5-25%, C as a slag forming agent
aF, 5-25%, A40s 2-30%, MgO3
~30%, 81025~25%, and as an alloying agent and deoxidizing agent C0.5% or less, SiO, 2~3.0%, Mn 1
.. 9-11.5%, Ni 0.4-4.5%, Cr 1.
3 to 10.2%, iron content 40% or less, and 1 as a slag forming agent.
A flux for submerged arc welding with a band-shaped electrode, containing 5% or less of one or both of TiO2 or ZrO2, with the remainder being unavoidable impurities. 4. CaO or CaCO35-25%, C as a slag forming agent
aF25-25%, A12os 2-30%, Mg03
~30%, 5i025~25%, SiO2~3.0% as an alloying agent and deoxidizing agent, Mn 1.9~11.5%
, NiO, 4-4.5%, Cr 1.3-10.2%,
Iron content 40% or less, and CO as an alloying agent 15% or less, 3
.. 6% or less Mo, 5.7% or less V 181 or more, 15% or less Tie as a sludge forming agent, or 1 of ZrO2
A strip-shaped electrode submerged arc welding flux containing one or two species, with the remainder consisting of unavoidable impurities.
JP10711081A 1981-07-10 1981-07-10 Flux for submerged arc welding by belt-like electrode Pending JPS589795A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP10711081A JPS589795A (en) 1981-07-10 1981-07-10 Flux for submerged arc welding by belt-like electrode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP10711081A JPS589795A (en) 1981-07-10 1981-07-10 Flux for submerged arc welding by belt-like electrode

Publications (1)

Publication Number Publication Date
JPS589795A true JPS589795A (en) 1983-01-20

Family

ID=14450718

Family Applications (1)

Application Number Title Priority Date Filing Date
JP10711081A Pending JPS589795A (en) 1981-07-10 1981-07-10 Flux for submerged arc welding by belt-like electrode

Country Status (1)

Country Link
JP (1) JPS589795A (en)

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6135510A (en) * 1984-07-27 1986-02-20 Agency Of Ind Science & Technol Molecular beam epitaxy growth method
JPS62500998A (en) * 1984-11-30 1987-04-23 アメリカン テレフオン アンド テレグラフ カムパニ− Chemical beam deposition method
JPH02280996A (en) * 1989-04-19 1990-11-16 Kobe Steel Ltd Bond flux for submerged arc welding
JPH02280995A (en) * 1989-04-19 1990-11-16 Kobe Steel Ltd Bond flux for submerged arc welding
JPH06277878A (en) * 1993-03-29 1994-10-04 Kobe Steel Ltd Flux for one-side submerged arc welding and welding process using the same
JP2002336991A (en) * 2001-05-15 2002-11-26 Nippon Steel Corp Submerged arc welding method for duplex stainless steel
CN103358054A (en) * 2012-04-10 2013-10-23 机械科学研究院哈尔滨焊接研究所 Coating for removing slag on laser cutting reverse side of thick steel plate
CN104308394A (en) * 2014-09-15 2015-01-28 安徽鸿路钢结构(集团)股份有限公司 Steel flux and application process thereof
CN104772580A (en) * 2014-01-15 2015-07-15 日铁住金溶接工业株式会社 Multi-electrode single-side submerged-arc welding bond flux
JP2016040047A (en) * 2014-08-11 2016-03-24 日鐵住金溶接工業株式会社 Bonded flux for submerged arc buildup welding

Cited By (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6135510A (en) * 1984-07-27 1986-02-20 Agency Of Ind Science & Technol Molecular beam epitaxy growth method
JPH0137847B2 (en) * 1984-07-27 1989-08-09 Kogyo Gijutsuin
JPS62500998A (en) * 1984-11-30 1987-04-23 アメリカン テレフオン アンド テレグラフ カムパニ− Chemical beam deposition method
JPH02280996A (en) * 1989-04-19 1990-11-16 Kobe Steel Ltd Bond flux for submerged arc welding
JPH02280995A (en) * 1989-04-19 1990-11-16 Kobe Steel Ltd Bond flux for submerged arc welding
JPH06277878A (en) * 1993-03-29 1994-10-04 Kobe Steel Ltd Flux for one-side submerged arc welding and welding process using the same
JP2002336991A (en) * 2001-05-15 2002-11-26 Nippon Steel Corp Submerged arc welding method for duplex stainless steel
JP4672177B2 (en) * 2001-05-15 2011-04-20 新日鐵住金ステンレス株式会社 Submerged arc welding method for duplex stainless steel
CN103358054A (en) * 2012-04-10 2013-10-23 机械科学研究院哈尔滨焊接研究所 Coating for removing slag on laser cutting reverse side of thick steel plate
CN104772580A (en) * 2014-01-15 2015-07-15 日铁住金溶接工业株式会社 Multi-electrode single-side submerged-arc welding bond flux
JP2016040047A (en) * 2014-08-11 2016-03-24 日鐵住金溶接工業株式会社 Bonded flux for submerged arc buildup welding
CN104308394A (en) * 2014-09-15 2015-01-28 安徽鸿路钢结构(集团)股份有限公司 Steel flux and application process thereof

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