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JPH0242312B2 - - Google Patents
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JPH0242312B2 - - Google Patents

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Publication number
JPH0242312B2
JPH0242312B2 JP4247286A JP4247286A JPH0242312B2 JP H0242312 B2 JPH0242312 B2 JP H0242312B2 JP 4247286 A JP4247286 A JP 4247286A JP 4247286 A JP4247286 A JP 4247286A JP H0242312 B2 JPH0242312 B2 JP H0242312B2
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JP
Japan
Prior art keywords
content
welding rod
welding
core wire
coating material
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
JP4247286A
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Japanese (ja)
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JPS62199294A (en
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Priority to JP4247286A priority Critical patent/JPS62199294A/en
Publication of JPS62199294A publication Critical patent/JPS62199294A/en
Publication of JPH0242312B2 publication Critical patent/JPH0242312B2/ja
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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] 本発明は低水素系被覆アーク溶接棒に関し、殊
に靭性の良好な溶接金属が得られる低水素系被覆
アーク溶接棒に関するものである。 [従来の技術] LPGタンク、圧力容器、寒冷地向け海洋構造
物等の大型構造物については安全性確保の要求が
特に強い為、それらの構造物における溶接部は、
良好な脆性破壊発生特性を有することが要求され
ている。要求特性値としては、従来汎用されてい
るシヤルピー衝撃値に加え、(1)脆性破壊発生温度
と関連を有するシヤルピー衝撃試験での破面遷移
温度(vTrS)、(2)COD(Crack Opening
Displacement;亀裂先端での開口変位)概念の
導入による設計温度でのCOD値等を代表的なも
のとして挙げることができる。上記の様な大型構
造物は、自動乃至半自動溶接機の適用によつて効
率的溶接を行なつているが上記要求特性との関係
上、Mn、Ni、B等の合金を含む低水素系溶接棒
による小入熱(例えば20kj/cm程度)溶接を行な
う部分も多く残されており、次に述べる様な問題
が指摘されている。 [発明が解決しようとする問題点] 即ち上記の様な従来技術では、溶接部の靭性が
不安定である他、小入熱であることに起因して溶
接能率が悪い等の問題があり、高靭性且つ高能率
な溶接棒の開発が強く要望されている。 従つて本発明の目的は大入熱であつても高靭性
が得られ、それによつて溶接能率を向上させるこ
とを可能にした被覆アーク溶接棒を提供しようと
するものである。 [問題点を解決する為の手段] 本発明の低水素系被覆アーク溶接棒は、N:
0.005%(重量%、以下同じ)以下の鋼心線外周
に、金属炭酸塩をCO2換算で8〜28%、金属弗化
物をF2換算で2〜12%含み、更に少なくとも脱
酸剤及びスラグ形成剤を配合してなる被覆剤を被
覆し、 且つ 被覆率A=被覆重量/棒重量×100:20〜45% [溶接棒のP含有率]=[心線中のP含有率]×100−
A/100+[被覆剤中のP含有率]×A/100≦0.01% [溶接棒のMn含有率]=[心線中のMn含有率]×100−
A/100+[被覆剤中のMn含有率]×A/100≦1.9% [溶接棒のNi含有率]=[心線中のNi含有率]×100−
A/100+[被覆剤中のNi]×A/100≦4% [溶接棒のNi+Mn含有率]=1.2〜4.3%である
点に要旨を有するものである。 [作用] 本発明者らは、大入熱溶接であつても−60℃以
下の破面遷移温度(vTrS)、及び−60℃での0.5
mm以上のCOD値が得られる被覆アーク溶接棒に
ついて、鋼心線と被覆剤の両面から種々検討し
た。その結果、心線のNを0.005%以下、被覆
率を20〜45%、被覆剤中のCO2を8%以下として
溶接金属中のNを0.01%以下に抑えてフエライト
粒の粗大化を防止すること、溶接棒全体のPを
0.01%以下に抑えて大入熱溶接時における各溶接
パスの最終凝固部のPの偏析による脆化を防止す
ること、溶接棒のNi+Mnを1.2%以上としてフ
エライト粒の粗大化を防止すること、溶接棒全
体のMnを1.9%以下としてベイナイテイツクな針
状フエライトの析出を防止すること、溶接棒全
体のNiを4%以下、Ni+Mnを4.3%以下として、
大入熱溶接時における一次晶粒界の発達による粒
界破壊の発生を防止することによつて、脆弱な部
分がなく且つ均一な微細フエライトからなる溶接
金属が得られ、良好なvTrSとCOD値が得られる
ことを見出し、本発明を完成するに至つた。即ち
本発明は大入熱溶接での特異性に着目し且つ新し
い観点に立脚して達成されたものであり、本発明
に係る溶接棒の完成によつて、高能率な大入熱溶
接施工が実施されたとしても大型構造物の安全性
が十分確保され、溶接技術分野ひいては産業の発
展に大きく貢献するものである。 以下、本発明の各種構成要件について個別的に
説明する。 <被覆剤> 本発明の被覆剤は、金属炭酸塩をCO2換算で8
〜28%、金属弗化物をF2換算で2〜12%含み、
更に少なくとも脱酸剤及びスラグ形成剤を配合し
てなるものである。 金属炭酸塩とはCaCO3、MgCO3、BaCO3等を
指し、アーク中で分解してCO2を発生し、溶融金
属を大気から保護し大気の侵入を防止する為のも
のである。金属炭酸塩のCO2換算値が8%未満で
はガス発生量が不足するので溶接金属中へのNの
侵入量が増加し(第1図参照)、靭性が低下する
(第2図参照)、一方金属炭酸塩のCO2換算値が28
%を超えると、スラグの粘性が増加してビード外
観が劣化し、大入熱での立向溶接が困難となる。 金属弗化物とはCaF2、NaF、AlF3、BaF2等を
指し、スラグの粘性を調整して作業性を維持する
為のものである。金属弗化物がF2換算で2%未
満ではスラグの粘性が大きすぎてビード形状が劣
化し、大入熱での立向溶接が困難となる。一方金
属弗化物がF2換算で12%を超えると、アークが
不安定となり、特に低電流域での上向溶接でアー
クが短絡して溶接が困難となる。尚金属弗化物の
配合割合をF2換算としたのは、分析等の便宜を
考慮しただけである。 脱酸剤としてはAl、Mg等の単体金属、Fe−
Ti、Fe−Si、Fe−Al、Fe−Si−B等の鉄合金或
はSi−Mn、Ca−Si、Al−Mg等の合金から選ば
れる1種若しくは2種以上を必要に応じて20%ま
で配合することができる。 またスラグ形成剤としては、TiO2、SiO2
MgO、Al2O3、ZrO2等を、溶融金属の被覆並び
に粘性の調整を主目的として適宜添加することが
できる。 尚必要に応じ合金成分や鉄粉等を配合し得るこ
とは言うまでもない。 上述した様な被覆剤は、珪酸カリウムや珪酸ナ
トリウム等の粘結剤によつて混練され鋼心線の外
周に被覆される。 <鋼心線> 本発明において用いられる鋼心線は、合金成分
について格別の制限を受けないが、一般的にも不
純元素と考えられているNについて特にシビアな
制限があり、N:0.005%以下であることが必要
である。 低水素系溶接棒を用いる大入熱溶接では、被覆
中に多量の金属炭酸塩を含有していても大気中か
ら混入するNを完全に防止することは困難であ
り、本発明者等が実験によつて確認したところに
よると、鋼心線中のNと溶接金属中のNとの間に
は第3図の様にほぼ完全な比例関係が認められ
た。従つて溶接金属中のNを0.01%以下に抑制す
る為には心線中のNを0.005%以下にする必要が
ある。一方心線中のNが0.005%を超えると、前
記第2図に示す様にフエライト粒が粗大化して溶
接金属の靭性が著しく低下する。 本発明に用いる心線としては炭素鋼心線が一般
的であるが、必要に応じてSi、Mn、Ti、Al等の
脱酸性元素やNi、Cr、Mo、Cu等の元素を配合
したものであつてもよい。 <被覆率> 本発明における被覆率Aは、次式で表わされ、
被覆率Aが20〜45%の範囲内でなければならな
い。 被覆率A(%)=被覆重量/棒重量×100 即ち被覆率Aが20%未満では金属炭酸塩を被覆
剤中に多量に含んでいたとしても、保護筒が十分
形成されなくなつてシールド不良をおこし、第4
図に示す様に溶接金属中のNが増加し、その結果
前記第2図に示した様に靭性が低下する。他方45
%を超えると、高電流域においてアーク長が長く
なり、アーク切れを伴つてシールド不良をおこ
し、溶接金属中のNが増加して靭性が低下する。 <溶接棒中のP> [溶接棒のP含有率]は、0.01%以下にする必
要がある。即ち[溶接棒のP含有率]が0.01%を
超えると、大入熱溶接時における各溶接パスの最
終凝固部にPが偏析して第5図に示す様にCOD
値が著しく低下する。P含有率については当初心
線のみに着目していたが、被覆剤中にもPが多く
混入していることが判明し、溶接棒全体としてP
の含有率を抑えなければならないことを見出し
た。工業的な被覆剤原料を用いる場合には、被覆
剤中のP含有率は極力少ないときでも0.01%前後
であり、従つて溶接棒合体のPを0.01%以下に抑
える為には心線中のP含有率を0.008%以下にす
ることが望まれる。 <溶接棒のMn、Ni> また本発明においては[溶接棒のMn含有
率]:≦1.9%、[溶接棒のNi含有率]:≦4%及び
[溶接棒の(Mn+Ni)含有率]:1.2〜4.3%の各
条件を満足する必要がある。 NiはMn量に応じて適量添加できるが、Ni+
Mn含有率が1.2%未満では溶接金属のフエライト
粒が粗大化して靭性が低下する。Ni+Mn含有率
が4.3%を超えたり或はNi含有率が4%を超える
と、大入熱溶接では溶接金属の一次晶粒界が脆弱
になり、粒界破壊が生じて靭性が低下する(第6
図参照)。 一方Mn含有率が1.9%を超えると、溶接金属が
ベイナイテイツクなフエライト粒で構成されるよ
うになり、硬化してCOD値が低下する。尚Mnの
好ましい含有率は、0.3〜1.9%程度である。 MnとNiは、鋼心線又は被覆剤或は双方から添
加できるものであり、被覆剤中のMn源としては
金属Mn、Fe−Mn、Si−Mn等を一般的に用いる
ことができる。又本発明に係る溶接棒の様にスラ
グ塩基度が高い様な場合(金属炭酸塩、金属弗化
物ベースのいわゆる低水素系被覆剤であり、通常
塩基性となる)には、MnOやMnO2等のマンガ
ン酸化物は溶接中に還元されてMnと成り得るの
で、これらもMn源として活用できる。この場合
には別途添加されるMnと合わせて全Mn量とし
て計算すればよい。 [実施例] 第1表に示す様な各種化学成分の心線No.C1〜
C7を準備し、第2表に示す様な各種の溶接棒を
作成した。尚第2表中の溶接棒No.E1〜E7は本発
明で規定する各要件を全て満足する実施例であ
り、溶接棒No.G1〜G12はいずれかの要件を欠く
比較例である。第2表に示した各溶接棒を用い溶
接を行なつた。
[Industrial Field of Application] The present invention relates to a low-hydrogen coated arc welding rod, and particularly to a low-hydrogen coated arc welding rod from which weld metal with good toughness can be obtained. [Prior art] There is a particularly strong demand for ensuring safety for large structures such as LPG tanks, pressure vessels, and offshore structures for cold regions.
It is required to have good brittle fracture occurrence characteristics. In addition to the conventionally widely used Shapey impact value, the required characteristic values include (1) the fracture surface transition temperature (vTrS) in the Shapey impact test, which is related to the temperature at which brittle fracture occurs, and (2) COD (Crack Opening
A representative example is the COD value at the design temperature, which is based on the concept of displacement (opening displacement at the tip of a crack). Large structures such as those mentioned above can be efficiently welded using automatic or semi-automatic welding machines, but in relation to the required characteristics above, low hydrogen welding containing alloys such as Mn, Ni, B, etc. There are still many parts where welding with a small heat input (for example, about 20 kj/cm) using a rod remains, and the following problems have been pointed out. [Problems to be Solved by the Invention] In other words, in the prior art as described above, there are problems such as unstable toughness of the welded part and poor welding efficiency due to small heat input. There is a strong demand for the development of a welding rod with high toughness and high efficiency. SUMMARY OF THE INVENTION Accordingly, an object of the present invention is to provide a coated arc welding rod that can obtain high toughness even under large heat input, thereby improving welding efficiency. [Means for solving the problems] The low hydrogen-based coated arc welding rod of the present invention has N:
The outer periphery of the steel core wire is 0.005% (weight%) or less, contains 8 to 28% of metal carbonate in terms of CO2 , 2 to 12% of metal fluoride in terms of F2 , and further contains at least a deoxidizer and Coating with a coating compounded with a slag forming agent, and coverage ratio A = coating weight/rod weight x 100: 20 to 45% [P content of welding rod] = [P content in core wire] x 100−
A/100 + [P content in coating material] x A/100≦0.01% [Mn content in welding rod] = [Mn content in core wire] x 100-
A/100 + [Mn content in coating material] x A/100≦1.9% [Ni content in welding rod] = [Ni content in core wire] x 100-
A/100+[Ni in coating material]×A/100≦4% [Ni+Mn content of welding rod]=1.2 to 4.3%. [Function] The present inventors have found that even in high heat input welding, the fracture surface transition temperature (vTrS) is below -60℃, and the fracture surface transition temperature (vTrS) is 0.5 at -60℃.
We investigated various aspects of coated arc welding rods that can obtain COD values of mm or higher, from both the steel core wire and the coating material. As a result, the N in the weld metal was kept to 0.005% or less, the coating rate was 20 to 45%, the CO 2 in the coating was 8% or less, and the N in the weld metal was kept to 0.01% or less, preventing the coarsening of ferrite grains. The P of the entire welding rod should be
To prevent embrittlement due to segregation of P in the final solidified part of each welding pass during high heat input welding by suppressing it to 0.01% or less; To prevent coarsening of ferrite grains by keeping Ni + Mn in the welding rod to 1.2% or more; Preventing the precipitation of bainitic acicular ferrite by setting the Mn content of the entire welding rod to 1.9% or less, setting the Ni content of the entire welding rod to 4% or less, and setting Ni+Mn to 4.3% or less.
By preventing the occurrence of grain boundary fracture due to the development of primary grain boundaries during high heat input welding, weld metal with no weak parts and consisting of uniform fine ferrite can be obtained, resulting in good vTrS and COD values. The present inventors have discovered that the following can be obtained, and have completed the present invention. That is, the present invention has been achieved by focusing on the specificity of high heat input welding and based on a new perspective, and by completing the welding rod according to the present invention, highly efficient high heat input welding can be performed. Even if implemented, the safety of large structures will be sufficiently ensured and will greatly contribute to the development of welding technology and industry. Various constituent elements of the present invention will be individually explained below. <Coating agent> The coating agent of the present invention has a metal carbonate content of 8
~28%, containing 2-12% metal fluoride in terms of F2 ,
Furthermore, at least a deoxidizing agent and a slag forming agent are blended. Metal carbonates refer to CaCO 3 , MgCO 3 , BaCO 3 , etc., and are decomposed in an arc to generate CO 2 to protect molten metal from the atmosphere and prevent air from entering. If the CO 2 equivalent value of the metal carbonate is less than 8%, the amount of gas generated is insufficient, so the amount of N penetrating into the weld metal increases (see Figure 1), and the toughness decreases (see Figure 2). On the other hand, the CO 2 equivalent value of metal carbonate is 28
%, the viscosity of the slag increases, the bead appearance deteriorates, and vertical welding with large heat input becomes difficult. The metal fluoride refers to CaF 2 , NaF, AlF 3 , BaF 2 , etc., and is used to adjust the viscosity of the slag and maintain workability. If the metal fluoride content is less than 2% in terms of F 2 , the viscosity of the slag is too high and the bead shape deteriorates, making vertical welding difficult with large heat input. On the other hand, if the metal fluoride content exceeds 12% in terms of F2 , the arc becomes unstable, and the arc becomes short-circuited, making welding difficult, especially in upward welding in the low current range. The mixing ratio of the metal fluoride was expressed in terms of F 2 only for convenience of analysis and the like. As deoxidizers, single metals such as Al and Mg, Fe-
One or more types selected from iron alloys such as Ti, Fe-Si, Fe-Al, Fe-Si-B, etc., or alloys such as Si-Mn, Ca-Si, Al-Mg, etc. may be used as necessary. %. In addition, as a slag forming agent, TiO 2 , SiO 2 ,
MgO, Al 2 O 3 , ZrO 2 and the like can be appropriately added mainly for the purpose of coating the molten metal and adjusting the viscosity. It goes without saying that alloy components, iron powder, etc. can be added as necessary. The above-mentioned coating material is kneaded with a binder such as potassium silicate or sodium silicate and coated on the outer periphery of the steel core wire. <Steel core wire> The steel core wire used in the present invention is not subject to any particular restrictions on alloy composition, but there are particularly severe restrictions on N, which is generally considered an impurity element, and N: 0.005%. It is necessary that the following is true. In high heat input welding using a low hydrogen welding rod, it is difficult to completely prevent N from entering the atmosphere even if the coating contains a large amount of metal carbonate. As a result, it was confirmed that there was a nearly perfect proportional relationship between the N in the steel core wire and the N in the weld metal, as shown in Figure 3. Therefore, in order to suppress the N content in the weld metal to 0.01% or less, it is necessary to reduce the N content in the core wire to 0.005% or less. On the other hand, if the N content in the core wire exceeds 0.005%, the ferrite grains become coarse as shown in FIG. 2, and the toughness of the weld metal is significantly reduced. Carbon steel core wires are generally used as the core wires used in the present invention, but if necessary, deoxidizing elements such as Si, Mn, Ti, and Al, and elements such as Ni, Cr, Mo, and Cu may be added. It may be. <Coverage rate> Coverage rate A in the present invention is expressed by the following formula,
The coverage A must be within the range of 20-45%. Coverage rate A (%) = coating weight / rod weight x 100 In other words, if the coverage rate A is less than 20%, even if the coating material contains a large amount of metal carbonate, the protective tube will not be formed sufficiently and the shield will fail. 4th
As shown in the figure, N in the weld metal increases, and as a result, the toughness decreases as shown in Figure 2 above. the other 45
If it exceeds %, the arc length becomes long in the high current range, causing arc breakage and shielding failure, and N in the weld metal increases and toughness decreases. <P in the welding rod> [P content in the welding rod] must be 0.01% or less. In other words, if the [P content of the welding rod] exceeds 0.01%, P segregates in the final solidification part of each welding pass during high heat input welding, resulting in COD as shown in Figure 5.
The value drops significantly. Regarding the P content, we initially focused only on the core wire, but it turned out that a large amount of P was also mixed in the coating material, and the P content of the welding rod as a whole was
It was discovered that the content of When using industrial coating material raw materials, the P content in the coating material is around 0.01% even when it is as low as possible. It is desirable that the P content be 0.008% or less. <Mn, Ni in the welding rod> In the present invention, [Mn content in the welding rod]: ≦1.9%, [Ni content in the welding rod]: ≦4%, and [(Mn+Ni) content in the welding rod]: It is necessary to satisfy each condition of 1.2 to 4.3%. Ni can be added in an appropriate amount depending on the amount of Mn, but Ni+
If the Mn content is less than 1.2%, the ferrite grains of the weld metal will become coarse and the toughness will decrease. If the Ni + Mn content exceeds 4.3% or the Ni content exceeds 4%, the primary grain boundaries of the weld metal become brittle during high heat input welding, causing intergranular fracture and decreasing toughness ( 6
(see figure). On the other hand, if the Mn content exceeds 1.9%, the weld metal will be composed of bainitic ferrite grains, which will harden and reduce the COD value. The preferable content of Mn is about 0.3 to 1.9%. Mn and Ni can be added from the steel core wire, the coating material, or both, and metal Mn, Fe-Mn, Si-Mn, etc. can generally be used as the Mn source in the coating material. In addition, when the slag basicity is high like the welding rod according to the present invention (it is a so-called low hydrogen coating material based on metal carbonate or metal fluoride, and is usually basic), MnO or MnO 2 Since manganese oxides such as oxides can be reduced to Mn during welding, they can also be used as Mn sources. In this case, the total amount of Mn may be calculated by including Mn added separately. [Example] Core wire No.C1~ with various chemical components as shown in Table 1
C7 was prepared, and various welding rods as shown in Table 2 were made. Welding rods Nos. E1 to E7 in Table 2 are examples that satisfy all of the requirements defined by the present invention, and welding rods Nos. G1 to G12 are comparative examples that lack any of the requirements. Welding was performed using each welding rod shown in Table 2.

【表】【table】

【表】【table】

【表】【table】

【表】【table】

【表】 各溶接棒の直径は5mmであり、板厚32mmのアル
ミキルド鋼板にX開先を形成し、立向き姿勢で
200A(A・C)、60〜70KJ/cmの大入熱条件下に
溶接を行なつた。得られた溶接金属からシオルピ
ー衝撃試験片(2mmVノツチ)とCOD試験片
(疲労ノツチ)を採取し、各試験片について靭性
試験を行なつた。その結果を第3表に示す。
[Table] The diameter of each welding rod is 5 mm, and an X groove is formed on a 32 mm thick aluminum killed steel plate.
Welding was carried out under conditions of large heat input of 200 A (A/C) and 60 to 70 KJ/cm. Siopy impact test pieces (2 mm V notch) and COD test pieces (fatigue notch) were taken from the obtained weld metal, and a toughness test was conducted on each test piece. The results are shown in Table 3.

【表】【table】

【表】 第3表の結果から明らかな様に、本発明の実施
例である溶接棒No.E1〜E7のものを用いて溶接を
行なつた場合は、いずれも作業性が良好であり、
得られた溶接金属のvTrSは全て−60℃以下、−60
℃でのCOD値0.8mm以上と良好な靭性を示した。 一方溶接棒No.G1〜G12のものは本発明で規定
するいずれかの要件を欠いている為、下記に示す
様な問題が指摘される。 (1) 溶接棒No.G1のものを用いた場合はN:0.007
%の心線を使用しているので、溶接金属のフエ
ライト粒が粗大化して低靭性を示した。 (2) 溶接棒No.G2のものを用いた場合は溶接棒中
のP含有率が0.013%と高いので、Pの著しい
偏析を伴なつてCOD値が低い。 (3) 溶接棒No.G3及びG4のものを用いた場合は被
覆率Aが本発明で規定する範囲外であるので、
作業性が悪く、N含有率が増加して低靭性を示
した。 (4) 溶接棒No.G5のものを用いた場合はCO2換算
値が6.6%と少ないので、N含有率が増加して
低靭性を示した。 (5) 溶接棒No.G6のものを用いた場合はCO2換算
値が30.8%と多すぎる為に、又溶接棒No.G7の
ものは金属弗化物含有率が3%と少なすぎる為
に、いずれも凸ビードとなり機械試験を行なう
までもなかつた。 (6) 溶接棒No.G8のものを用いた場合は靭性は良
好であるが、金属弗化物を31%含有しているの
でアークが不安定であつた。 (7) 溶接棒No.G9のものを用いた場合は溶接棒の
Mn含有量が2.22%と高いので、溶接金属が硬
化して延性が低下し、COD値が低かつた。 (8) 溶接棒No.G10のものを用いた場合は溶接棒の
Ni+Mn含有率が1.06%と少ないので、溶接金
属のフエライト粒が粗大化して靭性が悪かつ
た。 (9) 溶接棒No.G11のものを用いた場合はNi含有率
が4%を超え、又Ni+Mn含有率が4.30%を超
える為、又溶接棒No.G12のものを用いた場合は
Ni+Mn含有率が4.3%を超える為に、いずれ
も一次晶粒界で破壊が生じ、vTrS、COD値共
に極端に悪い値を示した。 [発明の効果] 以上述べた如く本発明によれば既述の構成を採
用することによつて、大入熱であつても高靭性が
得られ、これにより溶接能率を著しく向上し得る
ものである。
[Table] As is clear from the results in Table 3, when welding was performed using welding rods No. E1 to E7, which are examples of the present invention, workability was good in all cases.
The vTrS of the obtained weld metals is all below -60℃, -60
It showed good toughness with a COD value of 0.8 mm or more at °C. On the other hand, welding rods No. G1 to G12 lack any of the requirements stipulated by the present invention, and therefore the following problems are pointed out. (1) When using welding rod No. G1, N: 0.007
%, the ferrite grains of the weld metal became coarse and showed low toughness. (2) When welding rod No. G2 is used, the P content in the welding rod is as high as 0.013%, so the COD value is low with significant segregation of P. (3) When using welding rods No. G3 and G4, the coverage ratio A is outside the range specified by the present invention, so
Workability was poor, N content increased, and toughness was low. (4) When welding rod No. G5 was used, the CO 2 equivalent value was as low as 6.6%, so the N content increased and showed low toughness. (5) When welding rod No. G6 is used, the CO 2 equivalent value is too high at 30.8%, and when welding rod No. G7 is used, the metal fluoride content is too low at 3%. In both cases, convex beads formed and there was no need to perform mechanical tests. (6) When welding rod No. G8 was used, the toughness was good, but the arc was unstable because it contained 31% metal fluoride. (7) When using welding rod No. G9, the welding rod
Since the Mn content was as high as 2.22%, the weld metal hardened and its ductility decreased, resulting in a low COD value. (8) When using welding rod No. G10, the welding rod
Since the Ni+Mn content was as low as 1.06%, the ferrite grains in the weld metal became coarse, resulting in poor toughness. (9) When welding rod No. G11 is used, the Ni content exceeds 4%, and the Ni + Mn content exceeds 4.30%, and when welding rod No. G12 is used,
Since the Ni+Mn content exceeded 4.3%, destruction occurred at the primary grain boundaries in all cases, and both the vTrS and COD values showed extremely poor values. [Effects of the Invention] As described above, according to the present invention, by employing the above-mentioned configuration, high toughness can be obtained even with large heat input, thereby significantly improving welding efficiency. be.

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

第1図は被覆剤中のCO2含有率と溶接金属中の
N含有率との関係を示すグラフ、第2図は心線中
のN含有率が溶接金属のvTrS及び−60℃のCOD
値に与える影響を示すグラフ、第3図は心線中の
N含有率と溶接金属中のN含有率との関係を示す
グラフ、第4図は被覆率Aと溶接金属中のN含有
率との関係を示すグラフ、第5図は溶接棒中のP
含有率が溶接金属のvTrS及び−60℃のCOD値に
与える影響を示すグラフ、第6図は溶接棒中の
Ni+Mn含有率が溶接金属のvTrS及び−60℃の
COD値に与える影響を示すグラフである。
Figure 1 is a graph showing the relationship between the CO 2 content in the coating material and the N content in the weld metal, and Figure 2 shows the relationship between the N content in the core wire and the vTrS of the weld metal and the COD at -60°C.
Figure 3 is a graph showing the relationship between the N content in the core wire and the N content in the weld metal, and Figure 4 is a graph showing the relationship between the coverage ratio A and the N content in the weld metal. Figure 5 is a graph showing the relationship between P in the welding rod.
Figure 6 is a graph showing the effect of content on vTrS of weld metal and COD value at -60℃.
Ni+Mn content is vTrS of weld metal and -60℃
It is a graph showing the influence on COD value.

Claims (1)

【特許請求の範囲】 1 N:0.005%(重量%、以下同じ)以下の鋼
心線外周に、金属炭酸塩をCO2換算で8〜28%、
金属弗化物をF2換算で2〜12%含み、更に少な
くとも脱酸剤及びスラグ形成剤を配合してなる被
覆剤を被覆し、 且つ 被覆率A=被覆重量/棒重量×100:20〜45% [溶接棒のP含有率]=[心線中のP含有率]×100−
A/100+[被覆剤中のP含有率]×A/100≦0.01% [溶接棒のMn含有率]=[心線中のMn含有率]×100−
A/100+[被覆剤中のMn含有率]×A/100≦1.9% [溶接棒のNi含有率]=[心線中のNi含有率]×100−
A/100+[被覆剤中のNi]×A/100≦4% [溶接棒のNi+Mn含有率]=1.2〜4.3% であることを特徴とする低水素系被覆アーク溶接
棒。
[Claims] 1 N: 0.005% (weight%, the same applies hereinafter) or less of metal carbonate on the outer periphery of the steel core wire, 8 to 28% in terms of CO2 ,
It is coated with a coating material containing 2 to 12% metal fluoride in terms of F2 , and further contains at least a deoxidizing agent and a slag forming agent, and coverage ratio A = coating weight/bar weight x 100: 20 to 45 % [P content in welding rod] = [P content in core wire] x 100−
A/100 + [P content in coating material] x A/100≦0.01% [Mn content in welding rod] = [Mn content in core wire] x 100-
A/100 + [Mn content in coating material] x A/100≦1.9% [Ni content in welding rod] = [Ni content in core wire] x 100-
A low hydrogen-based coated arc welding rod, characterized in that A/100+[Ni in coating material]×A/100≦4% [Ni+Mn content of welding rod]=1.2 to 4.3%.
JP4247286A 1986-02-26 1986-02-26 Low hydrogen coated electrode Granted JPS62199294A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP4247286A JPS62199294A (en) 1986-02-26 1986-02-26 Low hydrogen coated electrode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP4247286A JPS62199294A (en) 1986-02-26 1986-02-26 Low hydrogen coated electrode

Publications (2)

Publication Number Publication Date
JPS62199294A JPS62199294A (en) 1987-09-02
JPH0242312B2 true JPH0242312B2 (en) 1990-09-21

Family

ID=12637008

Family Applications (1)

Application Number Title Priority Date Filing Date
JP4247286A Granted JPS62199294A (en) 1986-02-26 1986-02-26 Low hydrogen coated electrode

Country Status (1)

Country Link
JP (1) JPS62199294A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6061712B2 (en) * 2013-02-07 2017-01-18 株式会社神戸製鋼所 Low hydrogen coated arc welding rod

Also Published As

Publication number Publication date
JPS62199294A (en) 1987-09-02

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