JPS6123076B2 - - Google Patents
Info
- Publication number
- JPS6123076B2 JPS6123076B2 JP4698879A JP4698879A JPS6123076B2 JP S6123076 B2 JPS6123076 B2 JP S6123076B2 JP 4698879 A JP4698879 A JP 4698879A JP 4698879 A JP4698879 A JP 4698879A JP S6123076 B2 JPS6123076 B2 JP S6123076B2
- Authority
- JP
- Japan
- Prior art keywords
- welding
- flux
- spatter
- weight
- amount
- 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
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/24—Selection of soldering or welding materials proper
- B23K35/30—Selection of soldering or welding materials proper with the principal constituent melting at less than 1550°C
- B23K35/3053—Fe as the principal constituent
- B23K35/308—Fe as the principal constituent with Cr as next major constituent
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Nonmetallic Welding Materials (AREA)
Description
本発明は、被覆アーク溶接棒や複合ワイヤの如
く、フラツクスと、金属心線及び/若しくは金属
ケースとで一体に構成された溶接材料に関し、特
にフラツクスと、金属心線又は金属ケースの少な
くともひとつにCrを含有する含Cr溶接材料にお
いて、溶接時に発生するスパツタを可及的に減少
した溶接材料に関するものである。
上記の様な含Cr溶接材料は、ステンレス系或
はCr−Mo系高張力鋼の溶接材料や硬化肉盛用の
溶接材料として優れた性能を有しており、その適
用分野は年々増加する傾向にある。
即ちステンレス鋼は耐食性、耐酸化性、耐熱性
等に優れているほか良好な加工性及び機械的性質
を有しており、石油化学、繊維工業、原子力産業
等の各種産業分野で広く使用されているので、含
Cr溶接材料の需要もこれに伴なつて増大すると
考えられる。また低合金耐熱鋼及び耐熱合金は、
火力発電並びに石油化学工業を中心とする高温高
圧利用分野等で、更に硬化肉盛用の溶接材料は土
木建築用、鉱山用、農業用等種々の分野で、夫々
利用拡大の傾向がみられる。
この様に含Cr溶接材料は多くの産業分野でそ
の優れた性能が生かされており、その需要が今後
も伸びていくことは明白である。ところがこれま
で用いられていた含Cr溶接材料は、溶接時に発
生する溶接ヒユーム中に有害な可溶性Crを含有
するという問題があり、溶接作業員の健康管理上
好ましくない。
これらに対し本出願人は先に特開昭52−114447
号及び同53−19154号を出願し、ヒユーム中の可
溶性Cr量を低減する技術を提案した。即ちこれ
らの技術は、含Cr溶接材料を構成するフラツク
ス中のNa及びK量を減少し、固着剤としてリチ
ウムシリケートを使用することにより、溶接ヒユ
ーム中の可溶性Cr量を可及的に減少することに
成功したものである。
本発明者等は、その後も上記公報所載の技術の
実用化を達成すべくまたその性能を一段と高める
べく、更に研究を進めてきた。その結果先に開発
した含Cr溶接材料は、溶着金属の機械的性質及
び耐食性等が良好で且つヒユーム中の可溶性Cr
量を大幅に低減できるものの、溶接工程で多量の
スパツタが発生し、実用化を達成するうえで障害
になることが判明した。
即ちスパツタの発生は、溶接構造物の美感を
損なう、スパツタの付着により耐食性が低下す
る、スパツタの除去に時間を要し溶接能率が低
下する、等種々の難点を惹起する。従つて溶接ヒ
ユーム中の可溶性Cr低減効果を実用面で有効に
発揮させる為には、同時にスパツタも低減し得る
様な対策を構じておく必要がある。
本発明は、上記の様な事情に着目し、溶接ヒユ
ーム中の可溶性Crを低減しつつ溶接作業性殊に
スパツタ発生等の障害も生じない様な含Cr溶接
材料の開発を期して鋭意研究を重ねた結果なされ
たもので、その構成とは、フラツクス中のNa及
びK成分をその酸化物に換算して1重量%以下に
抑え、ヒユーム中の可溶性Cr量を低減し得る様
にした含Cr溶接材料において、前記フラツクス
中に少なくともチタン酸カルシウムを1〜15重量
%含有させ、スパツタの発生を著しく減少したと
ころに要旨が存在する。
溶接時に発生するスパツタは、溶接条件(極
性及び電流値等)、溶接方法(アーク長及びワ
イヤ送給角度等)、及びフラツクスの成分組成
によつてその発生状況が相違するが、フラツクス
の成分組成については、生成するスラグの粘性を
低くしまたフラツクスを塩基性にした方が、スパ
ツタは減少すると言われている。
従つてスパツタを減少させる為には、フラツク
スの成分組成を上記の知見に沿つて調整するのが
最も近道と考えられる。ところが本発明の含Cr
溶接材料は、先に述べた如く可溶性Cr量を減少
する為にNa及びK成分の量を著しく減じている
から、一般的なスパツタ低減対策をそのまま本発
明に適用することはできない。
そこで本発明者等は、上記した従来の知見に拘
泥されることなく、ヒユーム中の可溶性Cr量の
減少及び溶接中のスパツタの減少の両面から、最
適のフラツクス成分組成を明確にすべく鋭意研究
を進めた結果、本発明に到達したものである。
まず本発明では、フラツクス中のNa及びK成
分をその酸化物(Na2O及びK2O)に換算して1
重量%以下に抑えることが前提となる。これは溶
接ヒユーム中の可溶性Cr量を低減させる為で、
数値限定の理由は特開昭52−114447号及び同53−
19154号で説明した通りである。
そして本発明では、上記フラツクス中に適量の
チタン酸カルシウムを添加する。即ちチタン酸カ
ルシウムは、含Cr溶接材料に要求される本来の
性能を損なうことなく、溶接時に発生するスパツ
タを減少させるのに不可欠の成分で、好適配合率
は全フラツクス中に1〜15重量%の範囲である。
チタン酸カルシウムの添加によつてスパツタが減
少する理由は、この中に含まれるCaO及びTiO2
が何れもアーク集中性を高める機能を有してお
り、且つスパツタ発生原因の1つであるガス発生
成分を含んでいない為と考えられる。これらの効
果を有意に発揮させる為には全フラツクス中に少
なくとも1重量%以上含有させる必要がある。し
かし15重量%を越えるとアークが絞られてビード
が凸気味になり、継手性能が低下するからこれ以
下に抑えるべきである。尚チタン酸カルシウムと
してはCaTiO3、CaTi3O7、Ca3Ti2O7等が挙げら
れ、またCaO:20〜50%、TiO2:15〜75%を含
む溶融フラツクスも適用でき更に同効物質として
チタン酸マグネシウムを代用することも可能であ
る。
この様に本発明ではフラツクス中に適量のチタ
ン酸カルシウムを配合することにより、スパツタ
を減少させた点に最大の特徴があるが、このほか
フラツクスに要求される本来の機能を有効に発揮
させ或はその機能を一段と高める為には、適量の
炭酸カルシウム、螢石、ルチール等を配合するこ
とが望まれる。即ち炭酸カルシウムはガス発生剤
としての機能を有しており、シールド効果を高め
るのに極めて有効である。しかし配合量が多すぎ
るとスパツタの発生量が増大してチタン酸カルシ
ウムの添加効果が薄れると共に、溶着金属中の炭
素量が増大し機械的性質が低下する傾向がある。
これらの点を考慮すると最も好ましい炭酸カルシ
ウムの配合量は10〜35重量%である。
螢石はスラグに流動性を付与すると共に溶接金
属のX線特性を高める効果がある。しかし多過ぎ
るとアークの集中性が低下してスパツタが増加す
る傾向があるので、通常は1〜15重量%の範囲か
ら選ばれる。
ルチールはアークをソフトにしてスパツタを一
段と低減するのに極めて有効であるが、多過ぎる
とスラグの流動性が過大になつてビード形状が劣
化するほかスラグの剥離性も低下してくるので、
通常は20〜60重量%の範囲から選択される。
このほか、フラツクス中に0.01重量%程度以上
の酸化ビスマスを配合すると、スラグの剥離性を
一段と高めることができるので有利である。しか
し配合量が多すぎるとビード形状が悪化し、且つ
それ自体他のフラツクス構成成分に比べて高価で
あるから、実用性を考慮すれば1重量%程度を上
限とすべきである。
尚本発明ではフラツクス中のNa及びK成分を
極力減少しなければならないから、最も一般的な
固着剤である珪酸ソーダや珪酸カリ等を用いるの
は好ましくなく、リチウムシリケート等を固着剤
として使用することが望まれる。
本発明は概略以上の様に構成されているが、要
はフラツクス中に適量のチタン酸カルシウムを配
合することによつて、スパツタの発生を著しく防
止し得たもので、殊にヒユーム中の可溶性Crを
低減すべくフラツクス中のNa及びK成分を減少
した含Cr溶接材料を実用化するうえで障害とな
るスパツタの問題を解消し得た意義は頗るきい。
次に本発明の実験例を示すが、下記は特許請求
の範囲に記載した実施態様と同様本発明を限定す
る性質のものではなく、前・後記の趣旨に沿つて
適当に変更して実施することも可能であり、それ
らはすべて本発明技術の範疇に含まれる。
実験例
第1表に示す如くチタン酸カルシウムの配合量
を変えたフラツクスを用い、固着剤としてリチウ
ムシリケート(SiO2:20重量%、Li2O:4重量
%)を使用し、これを金属心線(20%Cr−10%
Ni、4.0mmφ×350mml)に対し被覆径6.5mmφにな
る様に被覆して被覆アーク溶接棒を得た。
The present invention relates to a welding material such as a coated arc welding rod or a composite wire, which is integrally composed of a flux, a metal core wire, and/or a metal case, and particularly relates to a welding material that is integrally composed of a flux, a metal core wire, and/or a metal case, and more particularly, This invention relates to a Cr-containing welding material in which spatter generated during welding is reduced as much as possible. The above-mentioned Cr-containing welding materials have excellent performance as welding materials for stainless steel or Cr-Mo high-tensile steel and welding materials for hardfacing, and their application fields tend to increase year by year. It is in. In other words, stainless steel has excellent corrosion resistance, oxidation resistance, heat resistance, etc., as well as good workability and mechanical properties, and is widely used in various industrial fields such as petrochemicals, textile industry, and nuclear power industry. Since there are
It is thought that the demand for Cr welding materials will increase along with this. In addition, low alloy heat resistant steel and heat resistant alloys are
In addition to high-temperature and high-pressure fields such as thermal power generation and the petrochemical industry, welding materials for hardfacing are increasingly being used in various fields such as civil engineering, construction, mining, and agriculture. As described above, the excellent performance of Cr-containing welding materials is utilized in many industrial fields, and it is clear that the demand for them will continue to grow. However, the Cr-containing welding materials that have been used so far have the problem of containing harmful soluble Cr in the weld fume generated during welding, which is not desirable in terms of health care for welding workers. In response to these, the present applicant has previously published Japanese Patent Application Laid-Open No. 52-114447
No. 53-19154 and proposed a technology to reduce the amount of soluble Cr in hume. In other words, these techniques reduce the amount of soluble Cr in the welding fume as much as possible by reducing the amounts of Na and K in the flux that constitutes the Cr-containing welding material and by using lithium silicate as a fixing agent. It was successful. The inventors of the present invention have continued to conduct further research in order to achieve practical application of the technology described in the above-mentioned publication and to further improve its performance. As a result, the previously developed Cr-containing welding material has good mechanical properties and corrosion resistance of the weld metal, and also has soluble Cr in the fume.
Although it was possible to significantly reduce the amount of spatter, it was found that a large amount of spatter was generated during the welding process, which was an obstacle to achieving practical application. That is, the occurrence of spatters causes various problems, such as impairing the aesthetic appearance of the welded structure, reducing corrosion resistance due to the adhesion of spatters, and reducing welding efficiency as it takes time to remove the spatters. Therefore, in order to effectively demonstrate the effect of reducing soluble Cr in welding fume in practical terms, it is necessary to take measures to reduce spatter at the same time. The present invention has focused on the above-mentioned circumstances, and has carried out extensive research with the aim of developing a Cr-containing welding material that reduces soluble Cr in the welding fume and also improves welding workability and does not cause problems such as spatter. It was created as a result of repeated efforts, and its composition is a Cr-containing flux that suppresses the Na and K components in the flux to 1% by weight or less in terms of their oxides, and reduces the amount of soluble Cr in the fume. The gist of the welding material is that the flux contains at least 1 to 15% by weight of calcium titanate to significantly reduce the occurrence of spatter. The occurrence of spatter during welding varies depending on the welding conditions (polarity, current value, etc.), welding method (arc length, wire feeding angle, etc.), and the composition of the flux. It is said that spatter can be reduced by lowering the viscosity of the slag produced and by making the flux basic. Therefore, the shortest way to reduce spatter is to adjust the composition of the flux in accordance with the above findings. However, in the present invention, the Cr-containing
Since the welding material has significantly reduced amounts of Na and K components in order to reduce the amount of soluble Cr as described above, general spatter reduction measures cannot be directly applied to the present invention. Therefore, without being bound by the conventional knowledge described above, the present inventors conducted intensive research to clarify the optimal flux component composition from the viewpoint of reducing the amount of soluble Cr in the fume and reducing spatter during welding. As a result of these efforts, we have arrived at the present invention. First, in the present invention, the Na and K components in the flux are converted to their oxides (Na 2 O and K 2 O) and
It is a prerequisite that the amount must be kept below % by weight. This is to reduce the amount of soluble Cr in the welding fume.
The reason for numerical limitation is JP-A-52-114447 and JP-A No. 53-
As explained in issue 19154. In the present invention, an appropriate amount of calcium titanate is added to the flux. In other words, calcium titanate is an essential component for reducing spatter generated during welding without impairing the original performance required of Cr-containing welding materials, and the preferred blending ratio is 1 to 15% by weight in the total flux. is within the range of
The reason why spatter is reduced by adding calcium titanate is because of the CaO and TiO 2 contained in it.
This is thought to be because all of these have the function of increasing arc concentration and do not contain gas-generating components, which is one of the causes of spatter. In order to exhibit these effects significantly, it is necessary to contain at least 1% by weight or more in the total flux. However, if it exceeds 15% by weight, the arc becomes constricted and the bead becomes convex, degrading joint performance, so it should be kept below this range. Calcium titanate includes CaTiO 3 , CaTi 3 O 7 , Ca 3 Ti 2 O 7 and the like, and a molten flux containing CaO: 20-50% and TiO 2 : 15-75% can also be applied and has the same effect. It is also possible to substitute magnesium titanate as a substance. As described above, the greatest feature of the present invention is that spatter is reduced by incorporating an appropriate amount of calcium titanate into the flux. In order to further enhance its functionality, it is desirable to incorporate appropriate amounts of calcium carbonate, fluorite, rutile, etc. That is, calcium carbonate has a function as a gas generating agent and is extremely effective in enhancing the shielding effect. However, if the amount is too large, the amount of spatter will increase and the effect of adding calcium titanate will be weakened, and the amount of carbon in the weld metal will increase, which tends to deteriorate the mechanical properties.
Considering these points, the most preferred amount of calcium carbonate is 10 to 35% by weight. Fluorite has the effect of imparting fluidity to the slag and improving the X-ray characteristics of the weld metal. However, if the amount is too large, the arc concentration tends to decrease and spatter increases, so the amount is usually selected from the range of 1 to 15% by weight. Rutile is extremely effective in softening the arc and further reducing spatter, but if too much rutile is used, the fluidity of the slag becomes excessive, deteriorating the bead shape and reducing the peelability of the slag.
It is usually selected from the range of 20 to 60% by weight. In addition, it is advantageous to incorporate approximately 0.01% by weight or more of bismuth oxide into the flux because it can further improve the slag releasability. However, if the amount is too large, the bead shape will deteriorate, and the flux itself is more expensive than other flux components. Therefore, considering practicality, the upper limit should be about 1% by weight. In the present invention, since the Na and K components in the flux must be reduced as much as possible, it is not preferable to use the most common fixing agents, such as sodium silicate and potassium silicate, and instead use lithium silicate, etc. as the fixing agent. It is hoped that The present invention is generally constructed as described above, but the point is that by incorporating an appropriate amount of calcium titanate into the flux, the generation of spatter can be significantly prevented. The significance of being able to eliminate the problem of spatter, which is an obstacle to the practical application of Cr-containing welding materials with reduced Na and K components in the flux to reduce Cr, is significant. Next, experimental examples of the present invention are shown, but like the embodiments described in the claims, the following does not limit the present invention, and can be carried out with appropriate changes in accordance with the spirit of the above and below. All of these are within the scope of the present technology. Experimental Example Using fluxes with varying amounts of calcium titanate as shown in Table 1, lithium silicate (SiO 2 : 20% by weight, Li 2 O: 4% by weight) was used as a fixing agent, and this was attached to a metal core. Wire (20% Cr-10%
A coated arc welding rod was obtained by coating Ni, 4.0 mmφ x 350 mm l ) to a coating diameter of 6.5 mmφ.
【表】
得られた試験用含Cr溶接棒を用い、以下に示
す溶接条件、ヒユーム分析法、スパツタ採取法等
に基づいて試験を行なつた。
(1) 溶接条件:145A×20〜25V:A.C
(2) 母材:19mmt×75mmw×400mml:軟鋼
(3) ヒユーム分析法:
(採取法) 下部が開放され、上部にハイボリ
ユームエアサンブラーを有する鉄製の箱内で
夫々溶接しながら、エアサンブラーでヒユー
ムを吸引し、グラスフアイバー製の紙にて
ヒユームを採取する。
(分析法)
ヒユーム中の可溶性Cr:原子吸光法
フラツクス中のNa2O、K2O:原子吸光法
(4) スパツタ採取法:
軟鋼材上に上記溶接条件(速度は約25mm/
分)で長さ25cmの肉盛りビードを形成し、この
間に発生したスパツタを収集して秤量する。
(5) ビードの断面形状:
SUS304上に上記の溶接条件で肉盛りビード
を形成し、その断面形状を観察する。
結果を第2表に示す。[Table] Using the obtained Cr-containing welding rod for testing, tests were conducted based on the welding conditions, hume analysis method, spatter sampling method, etc. shown below. (1) Welding conditions: 145A x 20~25V: AC (2) Base metal: 19mm t x 75mm w x 400mm l : Mild steel (3) Humidity analysis method: (Sampling method) The lower part is open and the upper part is filled with high volume air. While welding in an iron box with a sampler, the air sampler sucks the fume and collects it using glass fiber paper. (Analysis method) Soluble Cr in fume: Atomic absorption method Na 2 O, K 2 O in flux: Atomic absorption method (4) Sputter collection method: Welding on mild steel material under the above welding conditions (speed of approximately 25 mm/min)
(min) to form a 25 cm long overlay bead, and collect and weigh the spatter generated during this time. (5) Bead cross-sectional shape: Form a built-up bead on SUS304 under the above welding conditions and observe its cross-sectional shape. The results are shown in Table 2.
【表】【table】
【表】
第2表の結果からも明らかな如く、フラツクス
中に適量のチタン酸カルシウムを配合すると、ヒ
ユーム中の可溶性Cr量を低く抑えたままでスパ
ツタを大幅に減少することができる。但しチタン
酸カルシウムの量が多すぎると(供試棒G)、ビ
ードが凸気味になつて継手性能が低下するので好
ましくない。[Table] As is clear from the results in Table 2, by incorporating an appropriate amount of calcium titanate into the flux, spatter can be significantly reduced while keeping the amount of soluble Cr in the hume low. However, if the amount of calcium titanate is too large (sample bar G), the bead becomes convex and the joint performance deteriorates, which is not preferable.
Claims (1)
ケースとで一体に構成され且つこれらの少なくと
もひとつにCrを含有し、更にフラツクス中のNa
及びK成分をその酸化物(Na2O及びK2O)に換
算して1重量%以下に抑えてなる溶接材料におい
て、前記フラツクス中に少なくとも下記の成分を
含有させてなることを特徴とする含Cr溶接材
料。 炭酸カルシウム:10〜35重量% 蛍石:1〜10重量% ルチール:20〜60重量% チタン酸カルシウム:1〜15重量%[Claims] 1. The flux is integrally formed with a metal core wire and/or a metal case, and at least one of these contains Cr, and the flux contains Na.
and a welding material in which the K component is suppressed to 1% by weight or less in terms of its oxides (Na 2 O and K 2 O), characterized in that the flux contains at least the following components: Cr-containing welding material. Calcium carbonate: 10-35% by weight Fluorite: 1-10% by weight Rutile: 20-60% by weight Calcium titanate: 1-15% by weight
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4698879A JPS55149796A (en) | 1979-04-16 | 1979-04-16 | Cr-contained welding material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP4698879A JPS55149796A (en) | 1979-04-16 | 1979-04-16 | Cr-contained welding material |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS55149796A JPS55149796A (en) | 1980-11-21 |
| JPS6123076B2 true JPS6123076B2 (en) | 1986-06-04 |
Family
ID=12762580
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP4698879A Granted JPS55149796A (en) | 1979-04-16 | 1979-04-16 | Cr-contained welding material |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS55149796A (en) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT385699B (en) * | 1985-03-27 | 1988-05-10 | Ki Polt I | ELECTRIC WIRE |
| US5120931A (en) * | 1991-04-12 | 1992-06-09 | The Lincoln Electric Company | Electrode and flux for arc welding stainless steel |
| US6339209B1 (en) | 1997-12-05 | 2002-01-15 | Lincoln Global, Inc. | Electrode and flux for arc welding stainless steel |
-
1979
- 1979-04-16 JP JP4698879A patent/JPS55149796A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS55149796A (en) | 1980-11-21 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US5580475A (en) | Flux-cored wire for gas shield arc welding with low fume | |
| KR100355369B1 (en) | Flux cored wire for arc-welding of austenitic stainless steel | |
| US2432773A (en) | Coated welding electrode | |
| JP3441821B2 (en) | Covered arc welding rod for austenitic stainless steel | |
| JP2637907B2 (en) | Flux cored wire | |
| JPS5913955B2 (en) | Composite wire for stainless steel welding | |
| JPH0420720B2 (en) | ||
| JP2592637B2 (en) | Flux-cored wire for austenitic stainless steel welding | |
| JPH06285672A (en) | Flux cored wire of titania base for gas-shielded arc welding | |
| JPS6123076B2 (en) | ||
| JP3339759B2 (en) | Titanium flux cored wire for gas shielded arc welding | |
| GB2155045A (en) | Flux cored wire electrodes | |
| US3733458A (en) | Flux cored electrode | |
| JPH0899192A (en) | Flux cored wire for gas shielded arc welding | |
| JPS5695495A (en) | Wire containing low fume flux for gas shielded welding | |
| JPH0242313B2 (en) | ||
| JP3765772B2 (en) | Stainless steel flux cored wire | |
| JPH03294093A (en) | Flux cored wire electrode for gas shielded arc welding | |
| JP2592951B2 (en) | Flux cored wire for ultra-fine diameter self-shielded arc welding | |
| JPS5847959B2 (en) | Low hydrogen coated arc welding rod | |
| JP2694034B2 (en) | Flux-cored wire for high current density gas shielded arc welding | |
| JPS61286090A (en) | Flux-cored wire for arc welding | |
| JPH05220594A (en) | Wire and coated electrode for gas shielding arc welding for high cr austenitic stainless steel | |
| JP2577714B2 (en) | Cr containing arc welding rod | |
| JPH01233094A (en) | Flux cored wire for gas shielded arc welding of stainless steel |