JPS5937720B2 - Low hydrogen type coated arc welding rod for fillet welding - Google Patents
Low hydrogen type coated arc welding rod for fillet weldingInfo
- Publication number
- JPS5937720B2 JPS5937720B2 JP14997680A JP14997680A JPS5937720B2 JP S5937720 B2 JPS5937720 B2 JP S5937720B2 JP 14997680 A JP14997680 A JP 14997680A JP 14997680 A JP14997680 A JP 14997680A JP S5937720 B2 JPS5937720 B2 JP S5937720B2
- Authority
- JP
- Japan
- Prior art keywords
- welding
- weight
- coating
- rod
- coated arc
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000003466 welding Methods 0.000 title claims description 51
- 239000001257 hydrogen Substances 0.000 title claims description 14
- 229910052739 hydrogen Inorganic materials 0.000 title claims description 14
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title description 7
- 239000011248 coating agent Substances 0.000 claims description 38
- 238000000576 coating method Methods 0.000 claims description 36
- 239000000463 material Substances 0.000 claims description 14
- 239000002184 metal Substances 0.000 claims description 9
- 229910052751 metal Inorganic materials 0.000 claims description 9
- 238000010304 firing Methods 0.000 claims description 7
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 5
- 229910001209 Low-carbon steel Inorganic materials 0.000 claims description 5
- 229910001512 metal fluoride Inorganic materials 0.000 claims description 5
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 4
- 150000003839 salts Chemical group 0.000 claims description 2
- 239000011324 bead Substances 0.000 description 16
- 239000002893 slag Substances 0.000 description 16
- 239000000203 mixture Substances 0.000 description 11
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 9
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 9
- 230000000694 effects Effects 0.000 description 9
- 238000000034 method Methods 0.000 description 6
- 230000007423 decrease Effects 0.000 description 5
- 230000001681 protective effect Effects 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 239000000377 silicon dioxide Substances 0.000 description 4
- 229910000640 Fe alloy Inorganic materials 0.000 description 3
- 229910052681 coesite Inorganic materials 0.000 description 3
- 229910052906 cristobalite Inorganic materials 0.000 description 3
- 238000005538 encapsulation Methods 0.000 description 3
- 239000002245 particle Substances 0.000 description 3
- 235000012239 silicon dioxide Nutrition 0.000 description 3
- 229910052682 stishovite Inorganic materials 0.000 description 3
- 229910052905 tridymite Inorganic materials 0.000 description 3
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminium flouride Chemical compound F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 2
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000005520 cutting process Methods 0.000 description 2
- 230000007547 defect Effects 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 230000005484 gravity Effects 0.000 description 2
- 239000011148 porous material Substances 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- 239000004034 viscosity adjusting agent Substances 0.000 description 2
- 229910002551 Fe-Mn Inorganic materials 0.000 description 1
- 229910017082 Fe-Si Inorganic materials 0.000 description 1
- 229910017133 Fe—Si Inorganic materials 0.000 description 1
- 229910045601 alloy Inorganic materials 0.000 description 1
- 239000000956 alloy Substances 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 229910001634 calcium fluoride Inorganic materials 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 229910052593 corundum Inorganic materials 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 230000001771 impaired effect Effects 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 235000019353 potassium silicate Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 238000012360 testing method Methods 0.000 description 1
- 229910001845 yogo sapphire Inorganic materials 0.000 description 1
Landscapes
- Nonmetallic Welding Materials (AREA)
Description
【発明の詳細な説明】
本発明は被覆アーク溶接棒に関し、特に被覆の保護筒と
しての機能を改善し、溶接作業性及び継手性能を高めた
低水素系のすみ肉溶接専用被覆アーク溶接棒に関するも
のである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a coated arc welding rod, and more particularly to a coated arc welding rod exclusively for fillet welding, which is a low-hydrogen type and has an improved function as a protective tube and improved welding workability and joint performance. It is something.
溶接能率及び継手性能を向上すべく種々の溶接方法及び
溶接材料が提案されており、水素脆化を抑えた低水素系
被覆アーク溶接棒についても多くの技術が開発されてい
る。Various welding methods and welding materials have been proposed to improve welding efficiency and joint performance, and many technologies have also been developed for low-hydrogen coated arc welding rods that suppress hydrogen embrittlement.
しかしながら溶接後の手直し(補修溶接)を含めた全溶
接所要時間の短縮及び継手性能の両面を満足するものは
少ない。特に低水素系すみ肉溶接被覆アーク溶接棒にお
いては、溶接時間を短縮すべく高電流溶接を行なうと被
覆が焼けて脆くなり、溶接中に脱落することがある。そ
の為被覆の保護筒としての機能が低下し、アークが不安
定になつて作業性が低下すると共にシールド不足によつ
てブローホール等の継手欠陥が発生し、更にはビードが
不揃いになつて等脚性が乱れる。またアーク雰囲気中に
大気中の水分等が混入し、低水素系溶接棒の特長である
耐水素脆性も害される。本発明者等は前述の様な事情に
着目し、継手性能を害することなく優れた溶接作業性が
得られる様な低水素系すみ肉溶接用被覆アーク溶接棒の
開発を期して、被覆剤の成分組成や被覆の物性等につい
て研究を進めてきた。However, there are few methods that satisfy both the shortening of the total welding time including post-weld modifications (repair welding) and the joint performance. Particularly in low-hydrogen fillet welding coated arc welding rods, when high current welding is performed to shorten the welding time, the coating burns and becomes brittle, and may fall off during welding. As a result, the function of the coating as a protective tube deteriorates, the arc becomes unstable and workability decreases, and joint defects such as blowholes occur due to insufficient shielding, and even beads become uneven. Legs become disordered. In addition, atmospheric moisture etc. get mixed into the arc atmosphere, impairing the hydrogen embrittlement resistance that is a feature of low-hydrogen welding rods. The present inventors focused on the above-mentioned circumstances, and with the aim of developing a low-hydrogen coated arc welding rod for fillet welding that would provide excellent welding workability without impairing joint performance, the present inventors developed a coating material. We have been conducting research on the component composition and physical properties of the coating.
本発明はかかる研究の結果完成されたものであつて、そ
の構成とは、SiO2:10〜20%(重量%:以下同
じ)、TiO2:5〜20%、鉄粉:15〜45%、炭
酸塩:5〜30%(但しMgCO3を除く炭酸塩の総和
が10%以下)、金属フッ化物:3〜15%、脱酸性金
属:3〜15%を含有する被覆剤を、軟鋼心線外周に塗
布し焼成してなる低水素系すみ肉溶接用被覆アーク溶接
棒であつて、焼成後の被覆剤の嵩密度を2.3〜3.3
1/d&Cしたところに要旨が存在する。本発明では、
被覆剤の成分組成を特定すると共に、焼成後における被
覆の嵩密度を特定範囲に設定することによつて溶接中の
被覆の脱落を防止し、保護筒としての本来の機能を保持
せしめることができた。The present invention was completed as a result of such research, and its composition is SiO2: 10 to 20% (weight %: the same below), TiO2: 5 to 20%, iron powder: 15 to 45%, carbonic acid A coating agent containing salt: 5 to 30% (however, the total carbonate excluding MgCO3 is 10% or less), metal fluoride: 3 to 15%, and deoxidizing metal: 3 to 15% is applied to the outer periphery of the mild steel core wire. A coated arc welding rod for low hydrogen fillet welding that is coated and fired, the bulk density of the coating material after firing being 2.3 to 3.3.
The gist lies in the 1/d&C. In the present invention,
By specifying the composition of the coating material and setting the bulk density of the coating within a specific range after firing, it is possible to prevent the coating from falling off during welding and maintain its original function as a protective tube. Ta.
その結果、等脚性及び耐水素脆性の優れた高品質の溶接
継手が作業性良く得られることになつた。以下本発明に
おける数値範囲設定の根拠を説明する。As a result, a high-quality welded joint with excellent isopodality and hydrogen embrittlement resistance was obtained with good workability. The basis for setting the numerical range in the present invention will be explained below.
SiO2:10〜20%
スラグの粘性調整剤として不可欠の成分であり、10%
未満ではスラグの粘性が低下し安定した被包性が得られ
ない。SiO2: 10-20% An essential component as a slag viscosity modifier;
If it is less than this, the viscosity of the slag decreases and stable encapsulation cannot be obtained.
一方20%を越えるとスラグの粘性が高くなりすぎて特
脚性が著しく劣化する。原料としては、珪砂、タルク、
マイカ或はその他の珪酸塩が用いられ、粘結剤として使
用される水ガラス中のSiO2も含まれる。TiO2:
5〜20%
スラグの被包性を決定する重要な成分で、5%未満では
スラグの被包性が悪くビードが凸状になる。On the other hand, if it exceeds 20%, the viscosity of the slag becomes too high, and its special characteristics deteriorate significantly. Raw materials include silica sand, talc,
Mica or other silicates are used, including SiO2 in water glass, which is used as a binder. TiO2:
5 to 20% This is an important component that determines the encapsulation of the slag. If it is less than 5%, the slag encapsulation is poor and the beads become convex.
また20%を越えるとスラグ量が多くなりすぎて2段ビ
ードが形成され易くなる。原料としてはルチールやイル
ミナイト等が使用される。鉄粉:15〜45%溶着金属
量を増大し溶接能率を高めるのに重要な成分であると共
に、すみ肉溶接専用棒として必要なビードの伸びを高め
る作用があり、15%未満ではこれらの効果が十分に発
揮されない。Moreover, if it exceeds 20%, the amount of slag becomes too large and two-stage beads are likely to be formed. Rutile, illuminite, etc. are used as raw materials. Iron powder: 15-45% It is an important component to increase the amount of deposited metal and improve welding efficiency, and it also has the effect of increasing the elongation of the bead, which is necessary as a fillet welding rod. If it is less than 15%, these effects will be reduced. is not fully demonstrated.
しかし45%を越えるとビードが凸状になり継手強度が
低下する。通常は鉄粉単独で使用されるが、Fe一Mn
やFe−Si等の鉄合金と併用することもできる。炭酸
塩:5〜30%
MgcO3−CacO3,BacO3が代表的なものと
して挙げられ、ガス発生剤としてシールド効果を発揮し
、耐ブローホール性及び耐ピツト性を高めると共に、大
気中の水分等の混入を防止して水素脆性の低下を防止す
る。However, if it exceeds 45%, the bead becomes convex and the joint strength decreases. Usually iron powder is used alone, but Fe-Mn
It can also be used in combination with iron alloys such as or Fe-Si. Carbonate: 5 to 30% MgcO3-CacO3 and BacO3 are typical examples, and they exert a shielding effect as a gas generating agent, increasing blowhole resistance and pitting resistance, and preventing contamination with atmospheric moisture, etc. This prevents deterioration of hydrogen embrittlement.
従つてルートキヤツプの大きいすみ肉溶接に通用する場
合は特に重要な成分となる。これらの効果を確保する為
には5%以上配合する必要があるが、30%を越えると
溶け込みが深くなつてアンダーカツトが発生し易くなる
。尚炭酸塩の中でもMgCO3が最も適当であり、これ
以外の炭酸塩(CacO3やBacO3等)の総和が1
0%を越えると、スラグが先行し2段ビードが形成され
易くなるので注意しなければならない。金属フツ化物:
3〜15%
金属フツ化物としては、CaF2、AlF3、MgF2
が用いられ気孔防止剤として不可欠の成分である。Therefore, it is a particularly important component when used for fillet welding with a large root cap. In order to ensure these effects, it is necessary to mix 5% or more, but if it exceeds 30%, the dissolution becomes deep and undercuts are likely to occur. Among carbonates, MgCO3 is the most suitable, and the sum of other carbonates (CacO3, BacO3, etc.) is 1.
If it exceeds 0%, slag tends to advance and two-stage beads are likely to be formed, so care must be taken. Metal fluoride:
3-15% Metal fluorides include CaF2, AlF3, MgF2
is used and is an essential ingredient as an anti-pore agent.
3%未満ではヒツト等の継手欠陥が発生する。If it is less than 3%, joint defects such as marks will occur.
しかし15%を越えるとスラグの粘性が低くなりすぎて
凸ビードになるので好ましくない。脱酸性金属:3〜1
5%MnlSisTilAlsMg或はこれらの鉄合金
が代表的なものとして挙げられ、3%未満では脱酸不足
によつてブローホールやアンダーカツトが発生し易く、
一方15%を越えると溶接金属が硬くなり耐割れ性が低
下する。However, if it exceeds 15%, the viscosity of the slag becomes too low, resulting in convex beads, which is not preferable. Deoxidizing metal: 3-1
Typical examples include 5%MnlSisTilAlsMg or iron alloys thereof; if it is less than 3%, blowholes and undercuts are likely to occur due to insufficient deoxidation;
On the other hand, if it exceeds 15%, the weld metal becomes hard and crack resistance decreases.
本発明では上記6成分を被覆剤の必須成分とするが、こ
のほか必要に応じて下記の成分を配合することもある。In the present invention, the above-mentioned six components are essential components of the coating material, but the following components may be added as necessary.
MgO:10%以下
ビード形状を滑らかにするのに有効であるが、10%を
越えると等脚性が著しく害される。MgO: 10% or less is effective in smoothing the bead shape, but if it exceeds 10%, isopodality is significantly impaired.
Al2O3:5%以下スラグの粘性調整剤として有効で
あるが、5%を越えると等脚性が劣化する。Al2O3: 5% or less is effective as a viscosity modifier for slag, but if it exceeds 5%, isopodity deteriorates.
合金粉:5%以下
溶接金属の機械的性質や耐食性等を改善する為に、目標
性能に応じてCUsMOsNisCr等の合金元素単体
或はこれらの鉄合金を添加することは極めて有効であり
、通常は5%以下の範囲で添加される。Alloy powder: 5% or less In order to improve the mechanical properties and corrosion resistance of weld metal, it is extremely effective to add single alloying elements such as CUsMOsNisCr or iron alloys of these, depending on the target performance. It is added in an amount of 5% or less.
本発明で使用する被覆剤の成分組成は上記の通りである
が、この被覆剤を軟鋼心線外周に塗布し焼成して得られ
る本発明溶接棒の性能は、被覆の耐脱落性と密接な関係
を有している。The composition of the coating material used in the present invention is as described above, but the performance of the welding rod of the present invention obtained by applying this coating material to the outer periphery of a mild steel core wire and firing it is closely related to the shedding resistance of the coating. have a relationship.
即ち先に説明した如く被覆は溶接時に保護筒を構成し、
アークを安定にすると共にシールド効果を高める作用が
あるが、溶接時に被覆が脱落すると上記の効果が失なわ
れる。そこで被覆の耐脱落性を改善すべく実験を行なつ
たところ、耐脱落性は焼成後の被覆の嵩密度と密接な関
係があり、嵩密度が2.3〜3.3g/dになる様に被
覆剤原料の粒度や製造条件等を設定すれば、優れた耐脱
落性を確保できることが分つた。ちなみに第1図は、上
記成分組成を満足する低水素系すみ肉溶接用被覆アーク
溶接棒における、被覆の嵩密度と溶接中の脱落回数及び
すみ肉溶接部の上脚の最小脚長との関係を示したグラフ
である。但しこの実験では、5.5鼎φ×700mm1
の供試棒を使用し、T型のすみ肉試験片に300A(A
.C.)でグラビテイー溶接を行なつた。また被覆の嵩
密度は次式により算出した。式中K:嵩密度(9/Cn
t)
G:溶接棒の両端を切断・除去した後の棒重量(9)
l:溶接棒の両端を切断・除去した後の棒長(C7rL
)
d:心線直径(CTrL)
D:被覆径((V7l)
第1図からも明らかな様に、嵩密度が2.3〜3.31
/Critを外れるものは被覆の脱落が著しいのに対し
、嵩密度が上記好適範囲のものの被覆の脱落は皆無であ
る。That is, as explained earlier, the coating constitutes a protective tube during welding,
It has the effect of stabilizing the arc and increasing the shielding effect, but if the coating falls off during welding, the above effects will be lost. Therefore, we conducted an experiment to improve the shedding resistance of the coating, and found that the shedding resistance is closely related to the bulk density of the coating after firing, and that the bulk density was 2.3 to 3.3 g/d. It has been found that excellent shedding resistance can be ensured by setting the particle size of the coating material raw material, manufacturing conditions, etc. Incidentally, Figure 1 shows the relationship between the bulk density of the coating, the number of times it falls off during welding, and the minimum leg length of the upper leg of the fillet weld in a low-hydrogen coated arc welding rod for fillet welding that satisfies the above-mentioned composition. This is the graph shown. However, in this experiment, 5.5 diameter x 700 mm1
300A (A
.. C. ) gravity welding was performed. The bulk density of the coating was calculated using the following formula. In the formula, K: bulk density (9/Cn
t) G: Rod weight after cutting and removing both ends of the welding rod (9) l: Rod length after cutting and removing both ends of the welding rod (C7rL
) d: Core wire diameter (CTrL) D: Covering diameter ((V7l) As is clear from Figure 1, the bulk density is 2.3 to 3.31
In the cases where the bulk density falls outside of /Crit, the coating falls off significantly, whereas in the cases where the bulk density falls within the above-mentioned preferred range, the coating does not fall off at all.
尚直径5.5mm程度の被覆アーク溶接棒を用いたとき
の適正電流は通常230〜270A程度であるから、第
1図の実験データ(電流:300A)からも明らかな様
に、本発明の溶接棒は高溶接電流の条件奢こおいても高
い耐脱落性を発揮することが理解される。また上記好適
嵩密度範囲においては上脚部の脚長低下も少なく、高い
等脚性が得られる。尚上記嵩密度の好適範囲は、先に説
明した好適成分組成の被覆剤を使用した場合に限つて適
合するのであつて、異なる成分組成の被覆剤に対して同
列に論することはできない。Note that the appropriate current when using a coated arc welding rod with a diameter of about 5.5 mm is usually about 230 to 270 A, so as is clear from the experimental data (current: 300 A) in Fig. 1, the welding of the present invention It is understood that the rod exhibits high dropout resistance even under extreme conditions of high welding current. Further, within the above-mentioned preferred bulk density range, the leg length of the upper leg portion decreases little, and high isopodality is obtained. It should be noted that the preferred range of bulk density mentioned above is applicable only when a coating material having the above-described preferred component composition is used, and cannot be similarly discussed for coating materials having different component compositions.
その理由は、嵩密度が好適範囲にあつても、その成分組
成が異なれば生成されるスラグの粘性が異なつてくる為
、良好なビード形状が形成されなくなる為である。被覆
の嵩密度を調整する方法は特に限定されないが、最も一
般的なのは、1被覆剤原料の粒度構成を調整する方法、
2軟鋼心線外周へ塗布する際の圧力を調整する方法、3
上記1,2を組み合わせた方法・等が挙げられる。本発
明は以上の様に構成されており、被覆剤の成分組成を特
定すると共に、特に焼成後における被覆の嵩密度を特定
範囲に調整することによつて、被覆の耐脱落性を著しく
高め得ることになつた。The reason for this is that even if the bulk density is within a suitable range, if the component composition differs, the viscosity of the produced slag will differ, making it impossible to form a good bead shape. The method for adjusting the bulk density of the coating is not particularly limited, but the most common methods are: 1) adjusting the particle size structure of the coating material raw material;
2. Method of adjusting the pressure when applying to the outer periphery of the mild steel core wire, 3.
Examples include methods that combine the above 1 and 2. The present invention is configured as described above, and by specifying the component composition of the coating material and adjusting the bulk density of the coating within a specific range, particularly after firing, it is possible to significantly improve the shedding resistance of the coating. It became a matter of fact.
その結果高電流を適用した高速溶接が可能になると共に
、被覆の脱落に起因するシールド不足や等脚性の低下も
解消され、溶接能率及び継手性能向上の2大要求を一挙
に達成し得ることになつた。次に実験例を挙げて本発明
の構成及び作用効果を明確にする。実験例
第1表に示す成分組成の被覆剤(粒度構成は第2表の通
り)を、軟鋼心線(5.5nφ×700m“)の外周に
塗装圧60k9/c?il)速度270m/分で塗布し
、50〜100℃で1時間予備乾燥した後400℃で1
時間本焼成して、低水素系すみ肉溶接用被覆アーク溶接
棒を製造した。As a result, high-speed welding using high current becomes possible, and the lack of shielding and deterioration of isopodity caused by shedding of the coating are eliminated, achieving the two major requirements of welding efficiency and joint performance improvement all at once. It became. Next, experimental examples will be given to clarify the structure and effects of the present invention. Experimental Example A coating agent having the composition shown in Table 1 (particle size composition is as shown in Table 2) was coated on the outer periphery of a mild steel core wire (5.5nφ x 700m") at a pressure of 60k9/c?il and at a speed of 270m/min. After pre-drying at 50-100°C for 1 hour, drying at 400°C for 1 hour.
A coated arc welding rod for low hydrogen fillet welding was produced by main firing for an hour.
得られた各溶接棒を使用し、試験板(材質:SM−50
)断面形状:第2図)の水平すみ肉溶接線を運棒比1.
3でグラビテイ溶接し、溶接時における被覆の脱落回数
、ビードの最小上脚長及び溶接作業性を調べtに結果を
第1表に一括して示す。Using each obtained welding rod, a test plate (material: SM-50
)Cross-sectional shape: Figure 2) horizontal fillet weld line with a rod travel ratio of 1.
Gravity welding was carried out in Step 3, and the number of times the coating fell off during welding, the minimum upper leg length of the bead, and welding workability were investigated. The results are summarized in Table 1.
第1表より次の様に考察できる。(1)比較棒B−1,
2はSiO遣が規定範囲を外れたもので、不足の場合(
B−1)はスラグが先行してアンダーカツトが発生し、
過剰の場合(B−2)はスラグの粘性が高すぎて等脚性
が低下する。From Table 1, the following can be considered. (1) Comparison bar B-1,
2 indicates that the SiO amount is outside the specified range, and if there is a shortage (
In B-1), slag precedes and undercut occurs,
In the case of excess (B-2), the viscosity of the slag is too high and the isopodity is reduced.
(2)比較棒B−3,4はTiO2量が規定範囲を外れ
たもので、不足の場合(B−3)はスラグの被包性が乏
しくビードが凸状になり、過剰の場合(B−4)はスラ
グ量が多すぎて先行し2段ビードが形成される。(2) Comparison bars B-3 and B-4 have TiO2 content outside the specified range; in the case of insufficient TiO2 (B-3), the slag coverage is poor and the bead becomes convex; -4) The amount of slag is too large and a two-stage bead is formed in advance.
(3)比較棒B−5は鉄粉量が多すぎたもので、アーク
の広がりが小さくなつてビードが凸状になる。(3) Comparison bar B-5 contains too much iron powder, so the spread of the arc becomes small and the bead becomes convex.
(4)比較棒B−6,7は炭酸塩量が規定範囲を外れた
もので、不足の場合(B−6)はシールド不良によつて
ピツトが発生し、過剰の場合(Bー7)は溶け込みが深
くなつてアンダーカツトが発生する。(4) Comparison bars B-6 and B-7 have a carbonate content outside the specified range. In the case of insufficient carbonate (B-6), pitting occurs due to poor shielding, and in the case of excess (B-7) The penetration becomes deep and an undercut occurs.
尚比較棒B−8,9は、MgCO3以外の炭酸塩(Ca
cO3又はBaCO3)が10%を越えたもので、スラ
グの先行が起こり2段ビードになる。(5)比較棒B−
10,11は金属フツ化物量が規定範囲を外れたもので
、不足の場合(B−10)は気孔防止効果が不十分でピ
ツトが発生し、過剰の場合(B−11)はスラグの粘性
が高すぎて凸ビードになる。Comparison bars B-8 and 9 contain carbonates other than MgCO3 (Ca
cO3 or BaCO3) exceeding 10%, slag leads and becomes a two-stage bead. (5) Comparison bar B-
Nos. 10 and 11 are those in which the amount of metal fluoride is out of the specified range; when it is insufficient (B-10), the pore prevention effect is insufficient and pits occur, and when it is excessive (B-11), the viscosity of the slag is is too high, resulting in a convex bead.
(6)比較棒B−12〜16は脱酸性金属量が規定範囲
を外れたもので、不足の場合(B−12,13)は脱酸
不足によつてブローホール及びアンダーカツトが発生し
、過剰の場合(B−14,15,16)は溶接金属の耐
割れ性が悪い。(6) Comparison bars B-12 to B-16 have deoxidizing metal amounts outside the specified range, and in the case of insufficient deoxidizing metals (B-12, 13), blowholes and undercuts occur due to insufficient deoxidizing. In the case of excess (B-14, 15, 16), the cracking resistance of the weld metal is poor.
(7)比較棒B−17,18は被覆の嵩密度が規定範囲
を外れたもので、嵩密度が低すぎると(B一18)被覆
が脱落してアンダーカツト等が発生し、高すぎると(B
−17)被覆に縦割れが発生する。(7) Comparison bars B-17 and B-18 have coating bulk densities outside of the specified range; if the bulk density is too low (B-18), the coating will fall off and undercuts will occur; if it is too high, the coating will fall off and undercuts will occur. (B
-17) Vertical cracks occur in the coating.
(8)これらに対し本発明の要件を満足するA−1〜1
0の溶接棒は、被覆の脱落が起こらず良好な作業性が得
られ、ビードの等脚性も優れている。(8) A-1 to 1 that satisfy the requirements of the present invention for these
The No. 0 welding rod does not cause the coating to fall off, provides good workability, and has excellent isopodity of the bead.
Claims (1)
20重量%、鉄粉:15〜45重量%、炭酸塩:5〜3
0重量%(但しMgCO_3を除く炭酸塩の総和が10
重量%以下)、金属フッ化物:3〜15重量%、脱酸性
金属:3〜15重量%を含有する被覆剤を軟鋼心線外周
に塗布し焼成してなる低水素系すみ肉溶接用被覆アーク
塩溶棒であつて、焼成後の被覆剤の嵩密度が2.3〜3
.3g/cm^3であることを特徴とする低水素系すみ
肉溶接用被覆アーク溶接棒。1 SiO_2: 10~20% by weight, TiO_2: 5~
20% by weight, iron powder: 15-45% by weight, carbonate: 5-3
0% by weight (however, the total amount of carbonates excluding MgCO_3 is 10% by weight)
% by weight or less), metal fluoride: 3 to 15% by weight, and deoxidizing metal: 3 to 15% by weight, coated on the outer periphery of a mild steel core wire and fired. It is a salt melt rod, and the bulk density of the coating material after firing is 2.3 to 3.
.. A low-hydrogen coated arc welding rod for fillet welding, characterized by having a welding strength of 3 g/cm^3.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14997680A JPS5937720B2 (en) | 1980-10-24 | 1980-10-24 | Low hydrogen type coated arc welding rod for fillet welding |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP14997680A JPS5937720B2 (en) | 1980-10-24 | 1980-10-24 | Low hydrogen type coated arc welding rod for fillet welding |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5772791A JPS5772791A (en) | 1982-05-07 |
| JPS5937720B2 true JPS5937720B2 (en) | 1984-09-11 |
Family
ID=15486737
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP14997680A Expired JPS5937720B2 (en) | 1980-10-24 | 1980-10-24 | Low hydrogen type coated arc welding rod for fillet welding |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5937720B2 (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62173604A (en) * | 1986-01-27 | 1987-07-30 | Hitachi Ltd | Rotating magnetic head device for magnetic recording and reproducing equipment |
-
1980
- 1980-10-24 JP JP14997680A patent/JPS5937720B2/en not_active Expired
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS62173604A (en) * | 1986-01-27 | 1987-07-30 | Hitachi Ltd | Rotating magnetic head device for magnetic recording and reproducing equipment |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5772791A (en) | 1982-05-07 |
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