JPH11192585A - Coated electrode for austenitic stainless steel - Google Patents
Coated electrode for austenitic stainless steelInfo
- Publication number
- JPH11192585A JPH11192585A JP78698A JP78698A JPH11192585A JP H11192585 A JPH11192585 A JP H11192585A JP 78698 A JP78698 A JP 78698A JP 78698 A JP78698 A JP 78698A JP H11192585 A JPH11192585 A JP H11192585A
- Authority
- JP
- Japan
- Prior art keywords
- terms
- oxide
- stainless steel
- welding
- austenitic stainless
- 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
Links
- 229910000963 austenitic stainless steel Inorganic materials 0.000 title claims abstract description 16
- 238000003466 welding Methods 0.000 claims abstract description 55
- 239000011248 coating agent Substances 0.000 claims abstract description 17
- 238000006243 chemical reaction Methods 0.000 claims abstract description 16
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 11
- 239000000843 powder Substances 0.000 claims abstract description 8
- 229910001220 stainless steel Inorganic materials 0.000 claims abstract description 4
- 239000010935 stainless steel Substances 0.000 claims abstract description 4
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 4
- 229910052751 metal Inorganic materials 0.000 claims description 18
- 239000002184 metal Substances 0.000 claims description 18
- 229910001512 metal fluoride Inorganic materials 0.000 claims description 9
- 229910010413 TiO 2 Inorganic materials 0.000 claims description 6
- 230000001105 regulatory effect Effects 0.000 claims description 2
- 238000000576 coating method Methods 0.000 abstract description 7
- 229910052700 potassium Inorganic materials 0.000 abstract description 7
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 abstract description 5
- 230000004907 flux Effects 0.000 abstract 2
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 abstract 1
- 229910004742 Na2 O Inorganic materials 0.000 abstract 1
- 239000002893 slag Substances 0.000 description 19
- 239000010936 titanium Substances 0.000 description 19
- 239000011324 bead Substances 0.000 description 16
- 230000001681 protective effect Effects 0.000 description 14
- 230000000694 effects Effects 0.000 description 8
- 235000019353 potassium silicate Nutrition 0.000 description 6
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 5
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 5
- 235000011941 Tilia x europaea Nutrition 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 5
- 239000004571 lime Substances 0.000 description 5
- 239000011591 potassium Substances 0.000 description 5
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 5
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 4
- 239000010436 fluorite Substances 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 235000019738 Limestone Nutrition 0.000 description 3
- 238000011156 evaluation Methods 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 239000006028 limestone Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- 229910001200 Ferrotitanium Inorganic materials 0.000 description 2
- 229910000831 Steel Inorganic materials 0.000 description 2
- 239000000853 adhesive Substances 0.000 description 2
- 230000001070 adhesive effect Effects 0.000 description 2
- 238000007664 blowing Methods 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 230000036544 posture Effects 0.000 description 2
- 239000010959 steel Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- 229910004261 CaF 2 Inorganic materials 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 239000004111 Potassium silicate Substances 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- DLHONNLASJQAHX-UHFFFAOYSA-N aluminum;potassium;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Si+4].[Si+4].[Si+4].[K+] DLHONNLASJQAHX-UHFFFAOYSA-N 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- AYJRCSIUFZENHW-UHFFFAOYSA-L barium carbonate Chemical compound [Ba+2].[O-]C([O-])=O AYJRCSIUFZENHW-UHFFFAOYSA-L 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- WEUCVIBPSSMHJG-UHFFFAOYSA-N calcium titanate Chemical compound [O-2].[O-2].[O-2].[Ca+2].[Ti+4] WEUCVIBPSSMHJG-UHFFFAOYSA-N 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N iron oxide Inorganic materials [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 238000005121 nitriding Methods 0.000 description 1
- 238000005504 petroleum refining Methods 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 1
- 229910052913 potassium silicate Inorganic materials 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- LLZRNZOLAXHGLL-UHFFFAOYSA-J titanic acid Chemical compound O[Ti](O)(O)O LLZRNZOLAXHGLL-UHFFFAOYSA-J 0.000 description 1
Landscapes
- Arc Welding In General (AREA)
- Nonmetallic Welding Materials (AREA)
Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、オーステナイト系
ステンレス鋼用のライム系全姿勢被覆アーク溶接棒に係
り、特に全姿勢の溶接での溶接作業性、とりわけスラグ
剥離性と耐棒焼け性に優れたオーステナイト系ステンレ
ス鋼用被覆アーク溶接棒に関するものである。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a lime-based all-position coated arc welding rod for austenitic stainless steel, and in particular, has excellent welding workability in all-position welding, especially excellent slag peeling and rod burning resistance. And a coated arc welding rod for austenitic stainless steel.
【0002】[0002]
【従来の技術】オーステナイト系ステンレス鋼は、耐錆
性や耐食性,耐酸化性,耐熱性などの優れた特性によ
り、石油精製,化学,食品の各種プラント関連機器など
の構造物材として幅広く用いられている。このオーステ
ナイト系ステンレス鋼用の被覆アーク溶接棒についても
使用環境に合わせてその被覆剤の設計が行われており、
一般には、石灰石,蛍石を主成分としたライム系(lime
系)と、石灰石,ルチールを主成分としたライムチタニ
ア系(lime−titania 系)の被覆材料が使用されてい
る。特に、固定管などの全姿勢溶接(下向溶接のみなら
ず、重力の影響でビードが垂れ易い立向及び上向溶接を
含む溶接)にはライム系の被覆アーク溶接棒が使用され
ている。2. Description of the Related Art Austenitic stainless steel is widely used as a structural material for various plant-related equipment such as petroleum refining, chemical, and food due to its excellent properties such as rust resistance, corrosion resistance, oxidation resistance, and heat resistance. ing. Regarding the coated arc welding rod for austenitic stainless steel, the coating agent is designed according to the usage environment,
Generally, lime based on limestone and fluorite
And lime-titania coating materials mainly containing limestone and rutile. In particular, a lime-based coated arc welding rod is used for all-position welding of fixed tubes and the like (including not only downward welding but also vertical and upward welding in which beads are easily dropped due to the influence of gravity).
【0003】[0003]
【発明が解決しようとする課題】しかし従来の、オース
テナイト系ステンレス鋼用のライム系の被覆アーク溶接
棒では、主成分の蛍石によってスラグの粘性を高めるこ
とで立向溶接や上向溶接時にはビードが垂れることなく
良好なビード形状が得られるものの、蛍石含有量が多い
ことで交流溶接電源使用時にはアーク安定性が劣るこ
と、耐棒焼け性が不十分なために保護筒形状が不均一に
なり易いこと等の問題があった。また、下向溶接時には
ビード上にスラグが薄く被り、スラグの焼き付きが発生
してスラグ除去が非常に困難でこれに多大の手間がかか
っているのが実情である。However, in the conventional lime-based coated arc welding rod for austenitic stainless steel, the slag viscosity is increased by fluorite as a main component, so that the bead is used in vertical welding and upward welding. Good bead shape can be obtained without dripping, but the arc stability is inferior when AC welding power is used due to the high fluorite content, and the protection tube shape is uneven due to insufficient bar burning resistance. There was a problem that it was apt to become easily. Further, during downward welding, slag is thinly covered on the bead, and seizure of the slag occurs, which makes it very difficult to remove the slag, which requires a lot of trouble.
【0004】一方、このような耐棒焼け性やスラグ剥離
性を改善すべく、例えば特開昭53−52256号公報
で開示されるような改良型ライム系の被覆アーク溶接棒
も提案されてはいるものの、改善が十分でなく特にスラ
グ剥離性の点で満足できるものではない。On the other hand, in order to improve such bar burning resistance and slag peeling property, an improved lime-based coated arc welding rod as disclosed in, for example, JP-A-53-52256 has been proposed. However, the improvement is not sufficient and the slag removability is not particularly satisfactory.
【0005】このように、全姿勢で使用されるオーステ
ナイト系ステンレス鋼用被覆アーク溶接棒では、スラグ
剥離性、耐棒焼け性(保護筒形成性)、ビード形状、ア
ーク安定性及びスパッタの各項目で優れたもの、すなわ
ち溶接作業性が良好な被覆アーク溶接棒が要望されてい
る。[0005] As described above, in the coated arc welding rod for austenitic stainless steel used in all positions, each item of slag peeling property, bar burning resistance (protective cylinder forming property), bead shape, arc stability, and spatter. In other words, there is a demand for a coated arc welding rod having excellent welding workability.
【0006】そこで本発明の目的は、全姿勢での良好な
溶接作業性を有するオーステナイト系ステンレス鋼用被
覆アーク溶接棒を提供することにある。SUMMARY OF THE INVENTION An object of the present invention is to provide a coated arc welding rod for austenitic stainless steel having good welding workability in all positions.
【0007】[0007]
【課題を解決するための手段】前記の目的を達成するた
めに、本発明によるオーステナイト系ステンレス鋼用被
覆アーク溶接棒は、被覆剤全重量比で、金属フッ化物
(F換算値で):15〜30%、金属炭酸塩(CO2 換
算値で):10〜25%、K酸化物(K2 O換算値):
1〜5%、Ti又は/及びTi酸化物(TiO2 換算値
で):2〜8%、を必須成分として含有し、かつ、F
(換算値)/CO2 (換算値)の比:1.0〜1.5を
満足し、Na酸化物(Na2 O換算値で)を1%以下に
規制するとともに、金属粉末の含有量が30%以下であ
る被覆剤を、ステンレス鋼心線に被覆したものであるこ
とを特徴としている。In order to achieve the above-mentioned object, a coated arc welding rod for austenitic stainless steel according to the present invention has a metal fluoride (in F conversion value) of 15 by weight based on the total weight of the coating agent. 3030%, metal carbonate (in terms of CO 2 ): 10 to 25%, K oxide (in terms of K 2 O):
Contains 1 to 5%, Ti or / and / or Ti oxide (in terms of TiO 2 ): 2 to 8% as an essential component, and
(Converted value) / CO 2 (converted value) ratio: Satisfies 1.0 to 1.5, regulates Na oxide (in terms of Na 2 O) to 1% or less, and contains metal powder. Is 30% or less coated on a stainless steel core wire.
【0008】[0008]
【発明の実施の形態】本発明者は、前記目的を達成すべ
く、特に従来その改善が困難であった、耐棒焼け性とス
ラグ剥離性とに関し種々検討した。その結果、溶接中の
溶接棒端に片溶けや欠け落ちしない適正形状の保護筒を
形成すること、つまり良好な保護筒を形成しうる難易程
度を表す耐棒焼け性については、被覆溶接棒の溶融速度
を高めて耐棒焼け性の良化に有効な金属フッ化物と、含
有量が多いと溶接中の心線の抵抗発熱による加熱で分解
されて保護筒の形成を困難にする金属炭酸塩との比を特
定範囲に規制するとともに、被覆剤を心線に被覆するた
めの固着剤には欠け落ちしない適正形状の保護筒を形成
すべくK酸化物を含むカリ系の水ガラスを用いることに
より、耐棒焼け性を良好にしうることを知見した。ま
た、スラグ剥離性については、被覆剤にTi又は/及び
Ti酸化物を含有させることにより、前記の耐棒焼け性
を損なうことなくスラグ剥離性を良好にしうることを知
見した。BEST MODE FOR CARRYING OUT THE INVENTION In order to achieve the above object, the present inventor has made various studies on bar burning resistance and slag removability, which have been difficult to improve in the past. As a result, to form a protective cylinder of an appropriate shape that does not melt or chip off at the end of the welding rod during welding, that is, the bar burning resistance, which indicates the degree of difficulty in forming a good protective cylinder, A metal fluoride that increases the melting rate and is effective for improving bar burning resistance, and a metal carbonate that, when its content is large, is decomposed by heating due to resistance heating of the core wire during welding, making it difficult to form a protective cylinder Use a potassium-based water glass containing K oxide to form a protective cylinder of appropriate shape that does not chip off in the adhesive for coating the core wire with the coating agent while regulating the ratio to a specific range. It was found that the resistance to bar burning could be improved. In addition, as for slag releasability, it was found that slag removability can be improved without impairing the above-described bar burning resistance by adding Ti or / and Ti oxide to the coating agent.
【0009】これらの知見に基づいて前記特徴を有する
本発明はなされたものであり、以下に本発明における被
覆剤成分の限定理由について詳細に説明する。なお、被
覆剤各成分の含有量は被覆剤全重量比、すなわち、被覆
剤全重量に対する重量%である。The present invention having the above features has been made based on these findings, and the reasons for limiting the coating components in the present invention will be described in detail below. The content of each component of the coating agent is the weight ratio of the entire coating agent, that is,% by weight based on the total weight of the coating agent.
【0010】金属フッ化物をF換算値で15〜30
%:金属フッ化物は、被覆溶接棒の溶融速度を大きくす
る効果があり、また、スラグ生成剤としてスラグの流動
性を調整する効果がある。しかし15%未満ではそのよ
うな効果がなく、30%を超えるとアークが不安定にな
るとともにスラグの流動性が過剰となり、立向・上向姿
勢での溶接が困難となる。したがって、金属フッ化物量
は換算値で15〜30%の範囲とする。なお、金属フッ
化物としては、蛍石(CaF2),氷晶石(Na3AlF6 ),珪
フッカ化カリウム(K2SiF6)等が挙げられる。The metal fluoride is converted to an F-equivalent value of 15 to 30.
%: Metal fluoride has the effect of increasing the melting rate of the coated welding rod, and also has the effect of adjusting the fluidity of the slag as a slag forming agent. However, if it is less than 15%, such an effect is not obtained, and if it exceeds 30%, the arc becomes unstable and the fluidity of the slag becomes excessive, making it difficult to perform welding in a vertical or upward posture. Therefore, the amount of metal fluoride is set in a range of 15 to 30% in terms of a converted value. Examples of the metal fluoride include fluorite (CaF 2 ), cryolite (Na 3 AlF 6 ), potassium silicofluoride (K 2 SiF 6 ), and the like.
【0011】金属炭酸塩をCO2 換算値で10〜25
%:金属炭酸塩は、溶融金属の酸化や窒化を防ぐための
ガス発生剤としてCO2 ガスの発生によるシールド効果
がある。しかし、10%未満ではそのような効果がな
く、25%を超えると溶接中のステンレス鋼心線の抵抗
発熱によって被覆剤も加熱されることで金属炭酸塩の分
解が著しいために保護筒の形成が困難になり、その結
果、アークの集中性、指向性及び吹き付け力が悪化す
る。したがって、金属炭酸塩量はCO2 換算値で10〜
25%の範囲とする。なお、金属炭酸塩としては、石灰
石(CaCO3 ),炭酸マンガン(MnCO3 ),炭酸バリウム
(BaCO3 )等が挙げられる。The metal carbonate is converted to a CO 2 conversion value of 10 to 25.
%: Metal carbonate has a shielding effect due to generation of CO 2 gas as a gas generating agent for preventing oxidation or nitriding of the molten metal. However, if the content is less than 10%, such an effect is not obtained. If the content is more than 25%, the coating material is heated by the resistance heating of the stainless steel core wire during welding, and the decomposition of the metal carbonate is remarkable. And the arc concentration, directivity, and blowing force are deteriorated. Therefore, the metal carbonate content is 10 in terms of CO 2 value
The range is 25%. The metal carbonate includes limestone (CaCO 3 ), manganese carbonate (MnCO 3 ), barium carbonate (BaCO 3 ), and the like.
【0012】F換算値/CO2 換算値の比を1.0〜
1.5の範囲とする:本発明の最も特徴的構成であり、
全姿勢での良好な溶接作業性を得るためにはF換算値/
CO2換算値の比を前記の特定範囲に制限する必要があ
る。この比が1.0を下回ると耐棒焼け性が劣化(悪
化)し、強固で適正な形状の保護筒を形成することがで
きず、全姿勢での溶接が困難となる。一方、この比が
1.5を上回るとアーク安定性が劣化しスパッタも増大
する。したがって、F換算値/CO2 換算値の比を1.
0〜1.5の範囲に調整する。When the ratio of F conversion value / CO 2 conversion value is 1.0 to
1.5: the most characteristic configuration of the present invention;
To obtain good welding workability in all positions, the F conversion value /
It is necessary to limit the ratio of the CO 2 conversion value to the above specific range. If this ratio is less than 1.0, the stick burning resistance deteriorates (deteriorates), making it impossible to form a strong and appropriately shaped protective cylinder, making it difficult to weld in all positions. On the other hand, if this ratio exceeds 1.5, the arc stability deteriorates and spatter increases. Therefore, the ratio of F conversion value / CO 2 conversion value is set to 1.
Adjust to the range of 0 to 1.5.
【0013】K酸化物をK2 O換算値で1〜5%:被
覆アーク溶接棒は、所定量配合した被覆剤粉末に水ガラ
ス等の固着剤を加え混練して適度な粘性を与え、このも
のを心線に塗布し、次いで高温で焼成するという工程で
製造されている。この固着剤による心線への固着作用が
弱く不十分であると溶接中に保護筒の欠け落ちが発生
し、アークの集中性や指向性が悪く、アークが著しく不
安定でビード形状も悪くなる。一方、固着作用が強すぎ
ると保護筒も過剰に強固で、かつその長さが長くなり過
ぎ、このためアーク切れが発生する。そこで、適正な形
状で欠け落ちしない保護筒を形成すべく固着剤の種類及
び添加量について検討した。その結果、本発明における
被覆剤成分系では固着剤としてケイ酸カリ(K2SiO3)の
水溶液であるカリ系水ガラスが有効であることがわかっ
た。また、カリ長石などのK酸化物を添加した水ガラス
でも良好な保護筒を形成できることがわかった。このよ
うな理由により、K酸化物量はK2 O換算値で1〜5%
とする。なお、K酸化物としては、前記カリ系水ガラス
に含有されるものの他に、カリ長石(K2O・Al2O3 ・6SiO
2),カリガラス(CaO・K2O ・SiO2)等が挙げられる。K oxide is converted to KTwo1-5% in O equivalent:
The coated arc welding rod is used to apply water
Add a fixing agent such as water and knead to give appropriate viscosity.
Is applied to the core wire and then fired at a high temperature.
Being manufactured. The fixing action to the core wire by this fixing agent is
Insufficient weakness causes chipping of the protective sleeve during welding
The arc concentration and directivity are poor, and the arc
Stable and bad bead shape. On the other hand, the fixing action is too strong
In this case, the protective cylinder is too strong and its length is too long.
As a result, an arc break occurs. So, the proper shape
Type of adhesive to form a protective cylinder
And the amount added. As a result, in the present invention
Potassium silicate (KTwoSiOThree)of
Potassium-based water glass, which is an aqueous solution, proves to be effective
Was. Water glass to which K oxide such as potassium feldspar is added
However, it was found that a good protective cylinder could be formed. This
For this reason, the amount of K oxide is KTwo1 to 5% in O equivalent
And In addition, as the K oxide, the potassium-based water glass is used.
K feldspar (KTwoO ・ AlTwoOThree・ 6SiO
Two), Potash glass (CaO ・ KTwoO ・ SiOTwo) And the like.
【0014】Ti又は/及びTi酸化物をTiO2 換
算値で2〜8%:Tiは、従来は脱酸を目的に添加され
ていたが、本発明の被覆剤成分系においてはスラグ剥離
性を良好にしてスラグ除去を容易にする効果があり、こ
のことが新たに知見された。また、Ti酸化物の形態で
添加した場合も同様の効果が得られることがわかった。
この効果を得るには、Ti又は/及びTi酸化物の総計
で2%以上の添加量が必要である。一方、添加量が8%
を超えるとスパッタが増大し、また、立向溶接ではビー
ドが凸気味となってビード形状が不良となる。したがっ
て、Ti又は/及びTi酸化物の総計はTiO2 換算値
で2〜8%の範囲とする。なお、Tiは金属チタンのほ
か、フェロチタン(Fe−Ti)の形態で添加してもよ
く、また、Ti酸化物としては、ルチール(TiO2),イ
ルミナイト(FeO ・TiO2),チタン酸カリウム(K2Ti
O3),チタン酸カルシウム(CaTiO3)等が挙げられる。 2 to 8% of Ti or / and Ti oxide in terms of TiO 2 : Ti has conventionally been added for the purpose of deoxidation, but the coating agent component system of the present invention has poor slag release properties. This has the effect of making it easier to remove slag, which was newly found. It was also found that the same effect was obtained when Ti was added in the form of Ti oxide.
To obtain this effect, the total amount of Ti and / or Ti oxide must be 2% or more in total. On the other hand, the addition amount is 8%
If it exceeds, spatter increases, and in vertical welding, the bead becomes slightly convex and the bead shape becomes poor. Therefore, the total Ti and / or Ti oxide is 2 to 8 percent range in terms of TiO 2 value. Ti may be added in the form of ferro-titanium (Fe-Ti) in addition to metallic titanium. Ti oxides include rutile (TiO 2 ), illuminite (FeO.TiO 2 ), and titanic acid. Potassium (K 2 Ti
O 3 ) and calcium titanate (CaTiO 3 ).
【0015】Na酸化物をNa2 O換算値で1%以
下:Na酸化物はアークの安定性を劣化させるとともに
スパッタを増大させる。したがって、Na酸化物量はN
a2 O換算値で1%以下にする必要がある。なお、Na
酸化物としては固着剤として用いられる水ガラス中のNa
2OのようなNa酸化物が挙げられる。Na oxide is 1% or less in terms of Na 2 O: Na oxide degrades arc stability and increases spatter. Therefore, the amount of Na oxide is N
It must be 1% or less in terms of a 2 O. In addition, Na
Na in water glass used as a fixing agent as an oxide
Examples include Na oxides such as 2 O.
【0016】金属粉末が30%以下:Cr,Ni,M
o,Nbなどの金属粉末は、溶接金属の成分を調整する
ために適宜添加することができる。しかし、金属粉末の
量が30%を超えるとアークの吹き付け力が弱くなっ
て、アークが不安定になるとともにスパッタ量が多くな
る。よって金属粉末量は30%以下とする。Metal powder is 30% or less: Cr, Ni, M
Metal powders such as o and Nb can be appropriately added to adjust the components of the weld metal. However, if the amount of the metal powder exceeds 30%, the blowing force of the arc becomes weak, the arc becomes unstable, and the amount of spatter increases. Therefore, the amount of the metal powder is set to 30% or less.
【0017】[0017]
【実施例】表2に示す化学成分のオーステナイト系ステ
ンレス鋼心線に表3及び表4に示す組成の被覆剤を被覆
し、本発明例および比較例のオーステナイト系ステンレ
ス鋼用被覆アーク溶接棒を作製した。心線寸法は、直径
3.2mm,長さ300mmであり、被覆率(溶接棒全
重量に対する被覆剤重量)はいずれも30%とした。EXAMPLE An austenitic stainless steel core wire having the chemical composition shown in Table 2 was coated with a coating material having the composition shown in Tables 3 and 4, and coated arc welding rods for austenitic stainless steel of the present invention and comparative examples were obtained. Produced. The core wire dimensions were 3.2 mm in diameter and 300 mm in length, and the coverage (coating agent weight based on the total weight of the welding rod) was 30%.
【0018】各溶接棒について溶接作業性評価試験を行
った。試験は、板厚6mm×幅50mm×長さ300m
mの供試鋼板を用いてT型すみ肉継手を形成し、下向、
立向及び上向の各姿勢ですみ肉溶接を行って実施した。
下向溶接での溶接電流値は105A、立向及び上向溶接
での溶接電流値は85Aであり、いずれも交流溶接電源
を使用した。供試鋼板(オーステナイト系ステンレス
鋼)の化学成分を表1に示す。Each welding rod was subjected to a welding workability evaluation test. The test is 6mm thick x 50mm wide x 300m long.
A T-shaped fillet joint is formed using a test steel sheet of
Fillet welding was performed in each of the vertical and upward positions.
The welding current value in the downward welding was 105 A, and the welding current value in the vertical and upward welding was 85 A, and an AC welding power source was used in each case. Table 1 shows the chemical components of the test steel sheet (austenitic stainless steel).
【0019】試験の結果を表5及び表6に示す。評価
は、◎:非常に優れている、○:普通(実用上問題な
し)、△:少し劣る、×:劣る(実用不可能)、とし
た。The test results are shown in Tables 5 and 6. The evaluation was ◎: extremely excellent, :: normal (no problem in practical use), Δ: slightly inferior, ×: inferior (impractical).
【0020】[0020]
【表1】 [Table 1]
【0021】[0021]
【表2】 [Table 2]
【0022】[0022]
【表3】 [Table 3]
【0023】[0023]
【表4】 [Table 4]
【0024】[0024]
【表5】 [Table 5]
【0025】[0025]
【表6】 [Table 6]
【0026】表5から明らかなように、本発明例(溶接
棒No.1〜No.9)は、全姿勢で非常に良好な溶接
作業性(スラグ剥離性、耐棒焼け性、ビード形状、アー
ク安定性及びスパッタ量)が得られている。As is clear from Table 5, the present invention examples (welding rods No. 1 to No. 9) have very good welding workability (slag peeling property, bar burning resistance, bead shape, Arc stability and the amount of spatter).
【0027】一方、表6に評価結果を示す比較例(溶接
棒No.10〜No.18)では本発明で規定する要件
の何れかを欠くため、次のような問題があった。すなわ
ち、No.10は金属フッ化物量、及び、F換算値/C
O2 換算値の比が下限値を下回り、耐棒焼け性が著しく
劣化して悪く、ビード形状もやや悪くなっている。N
o.11はF換算値/CO2 換算値の比が上限値を上回
り、アーク安定性がやや劣化しスパッタ量もやや多くな
っている。No.12は金属フッ化物量、及び、F換算
値/CO2 換算値の比が上限値を上回り、特に立向・上
向溶接でのアーク安定性及びビード形状が著しく悪い。
No.13は金属炭酸塩が下限値を下回るためにシール
ド不足によってビード形状が悪く、Ti酸化物量(Ti
O2 換算値)が上限値を上回るためにスパッタ量が非常
に多く、また立向・上向溶接ではビードが凸気味で形状
不良であった。On the other hand, the comparative examples (welding rods No. 10 to No. 18) whose evaluation results are shown in Table 6 lack any of the requirements specified in the present invention, and therefore have the following problems. That is, No. 10 is the amount of metal fluoride, and F conversion value / C
The ratio of the O 2 conversion value is lower than the lower limit, the sticking resistance is remarkably deteriorated, and the bead shape is slightly deteriorated. N
o. In No. 11, the ratio of the F conversion value / CO 2 conversion value exceeds the upper limit value, the arc stability is slightly deteriorated, and the spatter amount is slightly increased. No. In No. 12, the ratio of the metal fluoride content and the F-converted value / CO 2 -converted value exceeds the upper limit, and particularly the arc stability and bead shape in vertical / upward welding are extremely poor.
No. No. 13 had poor bead shape due to insufficient shielding because the metal carbonate was below the lower limit, and the amount of Ti oxide (Ti
(In terms of O 2 ) exceeds the upper limit, the amount of spatter is very large, and in vertical / upward welding, the bead tends to be convex and the shape is poor.
【0028】また、No.14は金属炭酸塩が上限値を
上回るとともに、F換算値/CO2換算値の比が下限値
を下回るために耐棒焼け性が著しく悪く、全姿勢でアー
クが不安定でビード形状も悪化している。No.15は
K酸化物が上限値を上回るために保護筒が過剰に強固
で、かつその長さが長くなり過ぎることでアーク切れが
多発し、アークが著しく不安定となり、またNa酸化物
が上限値を上回るためにスパッタが多発した。No.1
6は金属粉末量が上限値を上回るためにアークの吹き付
け力が弱く、アークが著しく不安定になるとともにスパ
ッタ発生量もやや多かった。No.17はK酸化物が下
限値を下回るために耐棒焼け性が著しく悪く、溶接中に
保護筒の欠け落ちが発生してアークが極めて不安定とな
り、ビード形状も悪い。No.18はTi量がTiO2
換算値で下限値を下回るために、スラグ除去が極めて困
難であった。In addition, No. No. 14 shows that the metal carbonate exceeds the upper limit value and the ratio of F conversion value / CO 2 conversion value is lower than the lower limit value, so that the bar burning resistance is remarkably poor, the arc is unstable in all postures, and the bead shape deteriorates. ing. No. No. 15 shows that the protective cylinder is excessively strong because the K oxide exceeds the upper limit value, and that the length of the protective tube is too long, so that the arc is frequently broken, the arc becomes remarkably unstable, and the Na oxide becomes the upper limit value. Spatter occurred frequently. No. 1
In No. 6, since the amount of metal powder exceeded the upper limit, the arc spraying force was weak, the arc became extremely unstable, and the amount of spatter generated was somewhat large. No. In No. 17, since the K oxide falls below the lower limit value, the bar burning resistance is extremely poor, the protective tube is chipped off during welding, the arc becomes extremely unstable, and the bead shape is also poor. No. No. 18 has a Ti content of TiO 2
Since the converted value was below the lower limit, slag removal was extremely difficult.
【0029】[0029]
【発明の効果】以上述べたように、本発明のオーステナ
イト系ステンレス鋼用被覆アーク溶接棒によると、オー
ステナイト系ステンレス鋼の全姿勢での溶接において、
スラグ除去が容易で、耐棒焼け性(保護筒形成性)に優
れ、アーク安定性が良くビード形状が良好で、スパッタ
が少ないなど溶接作業性に優れており、固定管などの全
姿勢溶接での高能率化や溶接品質の向上に貢献すること
ができる。As described above, according to the coated arc welding rod for austenitic stainless steel of the present invention, in welding of austenitic stainless steel in all positions,
Easy slag removal, excellent bar burning resistance (protective tube formation), good arc stability, good bead shape, excellent welding workability with little spatter, and all-position welding of fixed pipes etc. It can contribute to higher efficiency of welding and improvement of welding quality.
Claims (1)
算値で):15〜30%、金属炭酸塩(CO2 換算値
で):10〜25%、K酸化物(K2 O換算値):1〜
5%、Ti又は/及びTi酸化物(TiO2 換算値
で):2〜8%、を必須成分として含有し、かつ、F換
算値/CO2 換算値の比:1.0〜1.5を満足し、N
a酸化物(Na2 O換算値で)を1%以下に規制すると
ともに、金属粉末の含有量が30%以下である被覆剤
を、ステンレス鋼心線に被覆したものであることを特徴
とするオーステナイト系ステンレス鋼用被覆アーク溶接
棒。1. A metal fluoride (in terms of F): 15 to 30%, a metal carbonate (in terms of CO 2 ): 10 to 25%, and a K oxide (K 2 O) Conversion value): 1
5%, Ti and / or Ti oxide (in terms of TiO 2 ): 2 to 8%, as an essential component, and a ratio of F converted value / CO 2 converted value: 1.0 to 1.5 Satisfy N
a The oxide (in terms of Na 2 O) is regulated to 1% or less, and a coating agent having a metal powder content of 30% or less is coated on a stainless steel core wire. Covered arc welding rod for austenitic stainless steel.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP78698A JPH11192585A (en) | 1998-01-06 | 1998-01-06 | Coated electrode for austenitic stainless steel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP78698A JPH11192585A (en) | 1998-01-06 | 1998-01-06 | Coated electrode for austenitic stainless steel |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH11192585A true JPH11192585A (en) | 1999-07-21 |
Family
ID=11483390
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP78698A Pending JPH11192585A (en) | 1998-01-06 | 1998-01-06 | Coated electrode for austenitic stainless steel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH11192585A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012143810A (en) * | 2011-01-14 | 2012-08-02 | Nippon Steel & Sumikin Welding Co Ltd | Low hydrogen covered electrode |
-
1998
- 1998-01-06 JP JP78698A patent/JPH11192585A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2012143810A (en) * | 2011-01-14 | 2012-08-02 | Nippon Steel & Sumikin Welding Co Ltd | Low hydrogen covered electrode |
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