JPH0462837B2 - - Google Patents

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Publication number
JPH0462837B2
JPH0462837B2 JP29455985A JP29455985A JPH0462837B2 JP H0462837 B2 JPH0462837 B2 JP H0462837B2 JP 29455985 A JP29455985 A JP 29455985A JP 29455985 A JP29455985 A JP 29455985A JP H0462837 B2 JPH0462837 B2 JP H0462837B2
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JP
Japan
Prior art keywords
weight
weld metal
welding
low
added
Prior art date
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Expired
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JP29455985A
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Japanese (ja)
Other versions
JPS62156097A (en
Inventor
Isao Nagano
Kunihide Yamane
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Nippon Steel Corp
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Nippon Steel Corp
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Priority to JP29455985A priority Critical patent/JPS62156097A/en
Publication of JPS62156097A publication Critical patent/JPS62156097A/en
Publication of JPH0462837B2 publication Critical patent/JPH0462837B2/ja
Granted legal-status Critical Current

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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、溶接作業性および低温じん性の良好
な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〕 近年、エネルギー資源開発の寒冷地化、深海化
を背景に溶接構造物は大型化、高性能化が進み溶
接継手に対する要求が一段と厳しくなり、貯蔵タ
ンクあるいは海洋構造物等はとりわけ低温じん性
の良好なことが必要である。この様な状況の中で
従来、低温じん性の良好な溶接継手を得るために
0.5%Niから3.5%Niまでの低水素系低Ni系溶接
棒が用いられてきた。例えば特開昭58−138591号
公報に示されるようにMgCO3−CaF2系の被覆剤
にSiCを添加することにより、耐ピツト性、ビー
ド形状およびビード外観が良好で溶接作業性のす
ぐれた低水素系被覆アーク溶接棒が知られてい
る。しかしながらこの溶接棒は作業性に重点をお
いて設計されているために低温におけるじん性を
確保するためには、比較的低溶接入熱で溶接して
溶接金属の組織を細粒化して高じん化を計るとい
う非能率的な施工法をとらなければならず、しか
も低溶接入熱に起因して母材の熱影響部が硬化す
るという問題点も生じてくる。さらにまた、じん
性を得るためのNiは高価であり溶接棒がコスト
高となり経済的でない欠点もある。 一方、通常の溶接入熱で溶接して低温じん性の
良好な継手が得られる低水素系被覆アーク溶接棒
として特公昭60−5397号公報に示されるように
CaCO3−CaF2系の被覆剤にTiおよびB2O3を添加
することにより溶接金属中に適当量のTiとBを
含有させて主にTiとBの効果で溶接金属の組織
の均一細粒化を計つて低温じん性を良好ならしめ
たものがある。 しかし、この溶接棒は溶接作業性が悪く、特に
水平すみ肉溶接ではビード形状が凸になるなどの
欠点がある。 さらに本発明者等は、良好な低温じん性を得
て、かつビード形状の凸状化防止対策に関してさ
きに特開昭59−4997号の発明を開示した。これは
主にTiO2、炭酸塩、弗化物の量を規制すること
によりビード外観、ビード形状を改良したもので
かなりの効果をみているが、この方法は被覆剤を
高塩基性寄りにする必要があるため必ずしも溶接
作業性(耐アンダーカツト性、スラグ剥離性)に
おいて十分満足できる結果が得られない面を残し
ている。 〔発明が解決しようとする問題点〕 本発明は、低温じん性の良好な溶接金属が得ら
れ、しかもビード形状、ビード外観おび溶接作業
性がすぐれた低水素系被覆アーク溶接棒を提供す
るものである。 〔問題点を解決するための手段〕 本発明は、前述の実情に対して種々の研究を重
ねた結果、開発された低水素系被覆アーク溶接棒
であつて、その要旨とするところはチタン酸化物
をTiO2に換算して13〜23重量%、Ti、Si、SiC、
Mg、Alの一種以上の合計を0.1〜8重量%、硼素
の酸化物または硼素の酸化物の化合物をB2O3
換算して0.05〜2重量%、MgCO34〜18重量%、
金属弗化物0.1〜17重量%、SiO21〜15重量%、
MgO9〜22重量%、Mn1〜10重量%、鉄粉10〜50
重量%を含有し、かつSiO2含有率をY(重量%)、
Ti+Si+SiC+Mg+Alで計算される脱酸剤含有
率をX(重量%)としたとき5≦Y+2X≦16なる
条件を満足し、更にNi0.5〜6.5重量%を含む被覆
剤に粘結剤を添加し、鋼心線に塗装してなる低水
素系被覆アーク溶接棒にある。 本発明の特徴はCO2源に主としてMgCO3を用
い(CaCO3、MnCO3等他の炭酸塩との併用も考
慮する)これにTiO2、MgOおよびSiO2を適量添
加することにより溶接作業性、ビード形状、ビー
ド外観を良化し、且つ硼素酸化物および硼素酸化
物の化合物にさらにTi、Si、SiC、Mg、Alの一
種以上を適量添加することによつて溶接金属中に
Ti、Bが一様に固溶され細粒の均一組織となつ
て、その溶接金属の低温じん性を著しく高めるも
のである。すなわち、MgCO3−CaF2系被覆剤は
CaCO3−CaF2系被覆剤に比べてSiO2を多量に添
加しており酸性寄りになつているため、前述のご
とく溶接作業性は良好である。 しかしながら、この被覆剤に強脱酸剤である
Ti、Si、SiC、Mg、Alの一種以上を添加するこ
とによりSiO2が還元され溶接金属中のSi量が多
くなりじん性を劣化させてしまうという欠点があ
る。この現象を防止するために本発明者等は前述
の様な知見に基づき、SiO2とTi、Si、SiC、Mg、
Alの関係を広範にわたつて比較検討したところ、
第1図に示される(B)の範囲に限定することによつ
て本発明の目的に合致し得る低温じん性の良好な
溶接金属が得られ、しかもビード形状、ビード外
観および溶接作業性が優れた性能を有する低水素
系被覆アーク溶接棒が得られるのである。 以下本発明について詳細に述べる。 〔作用〕 チタン酸化物としてはルチール、イルミナイ
ト、砂鉄、チタンスラグなどが用いられるが、ス
ラグ生成およびスラグの粘性を調整しスラグの被
包性を高める機能のほか、強脱酸剤であるSi、
Mg、Al、Ti、SiCの一種以上によつて溶接金属
中にTiを還元させるために添加するのであつて、
TiO2換算値で13重量%未満ではその効果がなく、
23重量%を超えて添加するとスラグの流動性が増
大してスラグが先行しビード形状が劣化するので
13〜23重量%の範囲が適当である。 Ti、Si、SiC、Mg、Alは強力な脱酸作用を有
しており酸化物を還元する。Tiを除くSi、SiC、
Mg、Alを被覆に添加することによりTiそのもの
を被覆中に添加しなくてもチタン酸化物が還元さ
れて溶接金属中に適量のTiを存在させることが
できる。またTiは脱酸のほか溶接金属中のBと
の関係で低温じん性を向上させるために添加する
ものであり、Ti、Si、SiC、Mg、Alの一種以上
の合計が0.1重量%未満ではその効果がなく、8
重量%を超えて添加するとスラグの流動性が悪く
なつてビード形状が劣化したり溶接金属が硬化し
低温じん性が劣化するので0.1〜8重量%の範囲
が適当である。なお、Ti、Si、Mg、AlはFe−
Ti、Fe−Si、Si−Mn、Al−Mgなどで添加され
る。 硼素の酸化物または硼素の酸化物の化合物は、
溶接金属にBを供給し、あわせて溶接金属中の
Tiとの関係で低温じん性を向上させるために添
加するものである。B2O3のような酸化された形
で被覆から添加する理由は、Fe−BなどのB合
金から溶接金属に添加すると偏析が生じ安定した
低温じん性が得られない場合があるためであり、
B2O3からBを還元して溶接金属に添加すること
により一様にBを分布させることができるため溶
接金属の組織の均一化が計れるのである。この場
合、硼素の酸化物または硼素の酸化物の化合物は
粘結剤である水ガラス中に添加して撹拌し、一様
に分散もしくは溶解させて被覆剤中に含有せしめ
ても同効果が得られることを確めている。硼素の
酸化物または硼素の酸化物の化合物の添加が
B2O3として0.05重量%未満であると溶接金属中
のBが少なく低温じん性の向上には効果がなく、
2重量%を超えて添加すると溶接金属中のBが多
くなり高温割れを生じ易くなり、低温じん性も低
下する。なお、ここでいう硼素の酸化物または硼
素の酸化物の化合物とは、硼砂、無水硼砂、天然
硼砂、灰硼石、カーン石などをさす。 MgCO3は、ガス発生剤として作用し、溶接金
属を大気から保護する効果を与えるものであり、
MgCO3が4重量%未満ではシールド不良が生じ
ピツトやブローホールが発生し易くなると共に窒
素ガスの吸収によつて溶接金属の低温じん性が低
下する。一方、18重量%を超えて添加するとアー
クが不安定になつてアーク切れを生じることがあ
るほか、スラグの粘性が増大してビード形状が凸
状になる。なお、CaCO3、SrCO3、MnCO3は、
MgCO3に準ずる作用を有するので、MgCO3の一
部をこれらのもので代替すなわち、MgCO3とこ
れらのものを併用しても相応の効果が得られる。 金属弗化物は溶接金属の拡散性水素量を減少さ
せると共に、ピツトやブローホールの発生を防止
する作用があり、金属弗化物が0.1重量%未満で
は前記の機能が有意に発揮されず、拡散性水素量
の増大によつて耐割れ性が低下し、錆、油脂、ペ
イント等によるピツトやブローホールが発生し易
くなる。一方、17重量%を超えて添加するとアー
クが不安定になるほか、スラグの流動性が過大に
なつてビード形状が劣化する。ここでいう金属弗
化物とは、CaF2、Na3AlF6、MgF2、AlF3など
をさす。 SiO2はスラグ生成剤および粘性調整剤として
の作用があり、特に粘性に大きな影響を与える成
分で1重量%未満ではスラグの流動状態が不安定
になつてビード外観が悪化したり、ビード形状が
凸形になる。一方、15重量%を超えて添加すると
スラグが硬くなり剥離が著しく困難になるほか、
酸性酸化物であるために塩基度が大幅に低下し溶
接金属のじん性が劣化する。 MgOはスラグ生成剤および粘性調整剤として
の作用があり、スラグの被包性を向上させる。9
重量%未満では前記の効果が有意に発揮されず、
スラグの粘性不足によつてアンダーカツトが発生
する。一方22重量%を超えて添加するとスラグの
粘性が増大して被包性が劣化しビード形状が凸形
になる。 Mnは金属マンガンあるいはフエロマンガン等
として添加され、脱酸剤あるいは合金剤として機
能のほか、溶接時のアークの強さ、およびアーク
の広がりを確保するために添加するが、1重量%
未満では溶接金属の機械的性質を十分に改善でき
ない。一方10重量%を超えて添加すると高温割れ
が発生するので好ましくない。 鉄粉はアーク安定性が向上すると共に溶着金属
量の増大によつて溶接能率を高めることができる
が、10重量%未満では溶接量が不足してビード伸
びが悪くなると共に溶接能率が悪い。一方50重量
%を超えて添加するとアークの広がりが阻害さ
れ、かつスラグの被包性が損なわれてビード形状
が凸形になる。 次にSiO2と強脱酸剤であるTi、Si、SiC、Mg、
Alの添加量を特定することが不可欠の要件であ
るが、適当なビード形状、ビード外観を確保し、
かつ良好な溶接金属の低温じん性を得るために
は、溶接金属中のSi量を考慮すべきであることが
確認された。即ち、第2図に溶接金属のvTrsに
およぼすSiの影響を調査した結果を示す。これに
よると溶接金属のSiが0.13〜0.38%の範囲におい
て低温じん性が大幅に改善できることが明らかで
ある。 そこで、本発明者等は前記の知見によりSiO2
と強脱酸剤であるTi、Si、SiC、Mg、Alとの量
的均衡の適正範囲を確認すべく検討した結果、
SiO2含有率をY(重量%)とし、また強脱酸剤含
有率のX(重量%)はX=Ti+Si+SiC+Mg+Al
としたとき 5Y+2X16 ……(1) を満足する必要がある。第1図は(1)式の条件と前
記SiO2と強脱酸剤の各条件を一つにまとめて表
示したグラフであつて、同図中のA部はSiO2
強脱酸剤がいずれも上限値以下という条件を満足
するが、Y+2X>16になつて(1)式を満足しない
領域である。同図中B部は全ての条件を満足する
領域である。同図中C部はSiO2と強脱酸剤がい
ずれも下限値以上という条件を満足するが、 Y+2X<5となつて(1)式を満足しない領域を
夫々示す。 すなわち、同図中B部においては低温じん性の
良好な溶接金属が得られるだけでなく、ビード形
状、ビード外観および溶接作業性が極めて良好で
ある。ところが同図中A部はY+2X>16の領域
であり、スラグが酸性寄りになつて溶接作業性は
良好になるが、SiO2が過剰に還元されて溶接金
属中のSi量が0.38%を超えてしまい低温じん性が
劣化するという欠点がある。他方同図中C部はY
+2X<5の領域であり、スラグの塩基性が高く
なつて溶接作業性が劣化すると共に、溶接金属中
のSi量が0.13%未満になつてしまい低温じん性も
劣化して所期の目的が達成されなくなる。 Niは溶接金属の強度、じん性を補充するため
に添加され、0.5重量%未満ではこれらの効果が
有効に発揮されない。しかしこれらの効果は6.5
重量%で飽和状態に達し、それ以上含有させても
じん性はほとんど向上せず、かえつて溶接作業性
が低下する。前記した各成分を配合した被覆剤
は、水ガラスなどの粘着剤を用いて鋼心線に通常
の溶接棒製造工程により塗装、乾燥などを行なつ
て製造することができるものである。 なお、本発明溶接棒に用いられる鋼心線とは
JIS G 3523の1種1号に相当する心線をさす。 次に実施例に基づいて本発明の効果をさらに具
体的に述べる。 〔実施例〕 第1表、第2表に示すように各種成分組成の被
覆剤に適量の水ガラスを混入し、これを5mmφ×
700mmの軟鋼心線に被覆、最高温度400℃で乾燥
し溶接棒A−1〜A−8、B−1〜B−11を試作
した。 前記の共試棒を用い板厚20mmのアルミキルド鋼
板に開先角度50°のV開先でルートギヤツプ1〜
3mmをとり、下向溶接を溶接電流220A、溶接入
熱18KJ/cmで行なつた。しかるのち最終パス側
の板厚表面下2mmより2mmVノツチシヤルピー衝
撃試験片を採取し−60℃にて試験を行なつた。溶
接作業性試験は、表面に20μmのウオツシユプラ
イマ塗布鋼板(板厚16mm)を水平すみ肉姿勢で、
溶接電流230A、運棒比1.3で行なつた。 判定基準は−60℃での衝撃値は5Kgf−m以上
を良好とした。また溶接作業性の○印は良好、△
印はやや不良、×印は不良を意味する。
[Industrial Field of Application] The present invention relates to a low-hydrogen coated arc welding rod that has good welding workability and low-temperature toughness. [Conventional technology] In recent years, with the development of energy resources in colder regions and deeper waters, welded structures have become larger and more sophisticated, and the requirements for welded joints have become even more severe, especially for storage tanks and offshore structures. Good low temperature toughness is required. Under these circumstances, conventional methods have been used to obtain welded joints with good low-temperature toughness.
Low hydrogen and low Ni welding rods ranging from 0.5% Ni to 3.5% Ni have been used. For example, as shown in JP-A No. 58-138591, by adding SiC to the MgCO 3 -CaF 2 coating material, it is possible to improve the pitting resistance, bead shape and bead appearance, and to improve welding workability. Hydrogen-based coated arc welding rods are known. However, this welding rod is designed with emphasis on workability, so in order to ensure toughness at low temperatures, it is necessary to weld with a relatively low welding heat input to make the weld metal microstructure finer and to create a high-dust structure. In addition, the low welding heat input causes the problem of hardening of the heat-affected zone of the base metal. Furthermore, Ni for obtaining toughness is expensive, and the welding rod is expensive, making it uneconomical. On the other hand, as shown in Japanese Patent Publication No. 60-5397, it is a low-hydrogen coated arc welding rod that can be welded with normal welding heat input to obtain joints with good low-temperature toughness.
By adding Ti and B 2 O 3 to the CaCO 3 -CaF 2 type coating material, appropriate amounts of Ti and B can be contained in the weld metal, and the structure of the weld metal can be made uniform and fine mainly due to the effects of Ti and B. There are some products that have good low-temperature toughness through granulation. However, this welding rod has disadvantages such as poor welding workability and a convex bead shape, especially in horizontal fillet welding. Furthermore, the present inventors have previously disclosed an invention in JP-A-59-4997 regarding measures to obtain good low-temperature toughness and to prevent the bead shape from becoming convex. This method mainly improves the bead appearance and bead shape by controlling the amounts of TiO 2 , carbonates, and fluorides, and has shown considerable effects, but this method requires the coating material to be highly basic. Therefore, it is not always possible to obtain fully satisfactory results in terms of welding workability (undercut resistance, slag removability). [Problems to be Solved by the Invention] The present invention provides a low-hydrogen coated arc welding rod that provides a weld metal with good low-temperature toughness and has excellent bead shape, bead appearance, and welding workability. It is. [Means for Solving the Problems] The present invention is a low-hydrogen coated arc welding rod developed as a result of various studies in response to the above-mentioned circumstances, and its gist is that titanium oxide 13 to 23% by weight converted to TiO2 , Ti, Si, SiC,
The total of one or more of Mg and Al is 0.1 to 8% by weight, boron oxide or boron oxide compound is 0.05 to 2% by weight in terms of B2O3 , MgCO3 is 4 to 18% by weight,
Metal fluoride 0.1-17% by weight, SiO2 1-15% by weight,
MgO9~22% by weight, Mn1~10% by weight, iron powder 10~50
% by weight, and the SiO 2 content is Y (% by weight),
When the deoxidizing agent content calculated by Ti + Si + SiC + Mg + Al is X (weight%), the following condition is satisfied: 5≦Y+2X≦16, and further a binder is added to the coating material containing 0.5 to 6.5 weight% of Ni, It is a low-hydrogen coated arc welding rod made by coating a steel core wire. The feature of the present invention is that MgCO 3 is mainly used as the CO 2 source (combined use with other carbonates such as CaCO 3 and MnCO 3 is also considered), and appropriate amounts of TiO 2 , MgO and SiO 2 are added to improve welding workability. , by improving the bead shape and bead appearance, and adding appropriate amounts of one or more of Ti, Si, SiC, Mg, and Al to boron oxide and boron oxide compounds.
Ti and B are uniformly dissolved in solid solution to form a fine-grained, uniform structure, which significantly improves the low-temperature toughness of the weld metal. In other words, the MgCO 3 −CaF 2 based coating is
Compared to the CaCO 3 -CaF 2 based coating, a large amount of SiO 2 is added and the coating is more acidic, so the welding workability is good as mentioned above. However, this coating is a strong deoxidizing agent.
Adding one or more of Ti, Si, SiC, Mg, and Al has the drawback that SiO 2 is reduced, increasing the amount of Si in the weld metal and deteriorating toughness. In order to prevent this phenomenon, the present inventors, based on the above-mentioned knowledge, combined SiO 2 with Ti, Si, SiC, Mg,
After a comprehensive comparative study of the relationship between Al,
By limiting the range to (B) shown in Figure 1, a weld metal with good low-temperature toughness that meets the purpose of the present invention can be obtained, and also has excellent bead shape, bead appearance, and welding workability. A low hydrogen-based coated arc welding rod with excellent performance can be obtained. The present invention will be described in detail below. [Function] Rutile, illuminite, iron sand, titanium slag, etc. are used as titanium oxides, but in addition to the function of adjusting slag formation and slag viscosity and improving slag encapsulation, Si is a strong deoxidizing agent. ,
It is added to reduce Ti in the weld metal by one or more of Mg, Al, Ti, and SiC,
If the TiO2 equivalent value is less than 13% by weight, there is no effect;
If more than 23% by weight is added, the fluidity of the slag will increase, causing the slag to take the lead and deteriorating the bead shape.
A range of 13 to 23% by weight is suitable. Ti, Si, SiC, Mg, and Al have strong deoxidizing properties and reduce oxides. Si excluding Ti, SiC,
By adding Mg and Al to the coating, titanium oxide is reduced and an appropriate amount of Ti can be present in the weld metal without adding Ti itself to the coating. In addition to deoxidizing, Ti is added to improve low-temperature toughness in relation to B in the weld metal. No effect, 8
If added in excess of 0.1% to 8% by weight, the fluidity of the slag will deteriorate, resulting in deterioration of the bead shape, hardening of the weld metal, and deterioration of low-temperature toughness, so a range of 0.1 to 8% by weight is appropriate. Note that Ti, Si, Mg, and Al are Fe−
It is added with Ti, Fe-Si, Si-Mn, Al-Mg, etc. Boron oxides or boron oxide compounds are
B is supplied to the weld metal, and at the same time
It is added to improve low-temperature toughness in relation to Ti. The reason why B 2 O 3 is added from the coating in an oxidized form is that if it is added to the weld metal from a B alloy such as Fe-B, it may cause segregation and make it impossible to obtain stable low-temperature toughness. ,
By reducing B 2 O 3 and adding it to the weld metal, it is possible to distribute B uniformly, thereby making it possible to make the structure of the weld metal uniform. In this case, the same effect can be obtained by adding the boron oxide or boron oxide compound to water glass as a binder, stirring it, uniformly dispersing or dissolving it, and incorporating it into the coating material. I am sure that it will be done. Addition of boron oxide or boron oxide compound
If it is less than 0.05% by weight as B 2 O 3 , there will be little B in the weld metal and it will not be effective in improving low temperature toughness.
Adding more than 2% by weight increases the amount of B in the weld metal, making it more likely to cause hot cracking and lowering the low-temperature toughness. Note that the boron oxide or boron oxide compound herein refers to borax, anhydrous borax, natural borax, perovorite, kernite, and the like. MgCO 3 acts as a gas generating agent and has the effect of protecting weld metal from the atmosphere.
If MgCO 3 is less than 4% by weight, shielding failure occurs, pits and blowholes are likely to occur, and the low-temperature toughness of the weld metal decreases due to absorption of nitrogen gas. On the other hand, if it is added in excess of 18% by weight, the arc may become unstable and arc breakage may occur, and the viscosity of the slag increases, resulting in a convex bead shape. In addition, CaCO 3 , SrCO 3 , MnCO 3 are
Since it has an effect similar to MgCO 3 , a corresponding effect can be obtained even if a part of MgCO 3 is replaced with these substances, that is, when MgCO 3 and these substances are used together. Metal fluoride has the effect of reducing the amount of diffusible hydrogen in the weld metal and preventing the formation of pits and blowholes. If the metal fluoride content is less than 0.1% by weight, the above function will not be achieved significantly, and the diffusibility will decrease. As the amount of hydrogen increases, cracking resistance decreases, making pits and blowholes more likely to occur due to rust, oil, paint, etc. On the other hand, if it is added in excess of 17% by weight, the arc becomes unstable and the fluidity of the slag becomes excessive, deteriorating the bead shape. The metal fluoride mentioned here refers to CaF 2 , Na 3 AlF 6 , MgF 2 , AlF 3 and the like. SiO 2 acts as a slag forming agent and a viscosity modifier, and is a component that has a particularly large effect on viscosity. If it is less than 1% by weight, the fluidity of the slag becomes unstable, resulting in poor bead appearance and bead shape. Becomes convex. On the other hand, if it is added in excess of 15% by weight, the slag becomes hard and peeling becomes extremely difficult.
Since it is an acidic oxide, the basicity decreases significantly and the toughness of the weld metal deteriorates. MgO acts as a slag forming agent and a viscosity modifier, improving the encapsulation of the slag. 9
If it is less than % by weight, the above effect will not be exhibited significantly,
Undercuts occur due to lack of slag viscosity. On the other hand, if it is added in an amount exceeding 22% by weight, the viscosity of the slag increases, the encapsulation properties deteriorate, and the bead shape becomes convex. Mn is added as metallic manganese or ferromanganese, etc., and is added to function as a deoxidizing agent or alloying agent, as well as to ensure arc strength and arc spread during welding, and is added at 1% by weight.
If it is less than that, the mechanical properties of the weld metal cannot be sufficiently improved. On the other hand, adding more than 10% by weight is not preferable because hot cracking occurs. Iron powder improves arc stability and increases welding efficiency by increasing the amount of deposited metal, but if it is less than 10% by weight, the amount of welding becomes insufficient, resulting in poor bead elongation and poor welding efficiency. On the other hand, if it is added in an amount exceeding 50% by weight, the spread of the arc will be inhibited, and the encapsulating properties of the slag will be impaired, resulting in a convex bead shape. Next, SiO 2 and strong deoxidizing agents Ti, Si, SiC, Mg,
It is essential to specify the amount of Al added, but it is also important to ensure an appropriate bead shape and appearance.
It was also confirmed that in order to obtain good low-temperature toughness of the weld metal, the amount of Si in the weld metal should be considered. That is, Figure 2 shows the results of investigating the influence of Si on vTrs of weld metal. According to this, it is clear that the low-temperature toughness can be significantly improved when the Si content of the weld metal is in the range of 0.13 to 0.38%. Therefore, based on the above findings, the present inventors
As a result of an investigation to confirm the appropriate range of quantitative balance between Ti, Si, SiC, Mg, and Al, which are strong deoxidizing agents,
Let the SiO 2 content be Y (wt%), and the strong deoxidizer content X (wt%) is X=Ti+Si+SiC+Mg+Al
When 5Y+2X16...(1) must be satisfied. Figure 1 is a graph that displays the conditions of equation (1) and the conditions of SiO 2 and the strong deoxidizing agent together. All of them satisfy the condition of being less than or equal to the upper limit value, but Y+2X>16, which is a region where equation (1) is not satisfied. Section B in the figure is an area that satisfies all the conditions. Section C in the figure indicates a region where both SiO 2 and the strong deoxidizer satisfy the condition that they are at least the lower limit, but where Y+2X<5 and the formula (1) is not satisfied. That is, in part B in the figure, not only a weld metal with good low-temperature toughness is obtained, but also the bead shape, bead appearance, and welding workability are extremely good. However, part A in the same figure is a region where Y+2X>16, and the slag becomes more acidic and welding workability becomes better, but SiO 2 is excessively reduced and the amount of Si in the weld metal exceeds 0.38%. The disadvantage is that low-temperature toughness deteriorates. On the other hand, part C in the same figure is Y
In the region of +2 will not be achieved. Ni is added to supplement the strength and toughness of the weld metal, and if it is less than 0.5% by weight, these effects will not be effectively exhibited. But these effects are 6.5
It reaches a saturation state at a weight percentage of 10% by weight, and even if it is contained beyond that level, the toughness hardly improves, and on the contrary, welding workability deteriorates. A coating material containing the above-mentioned components can be produced by coating a steel core wire with an adhesive such as water glass and drying the coated wire according to a normal welding rod manufacturing process. Furthermore, what is the steel core wire used in the welding rod of the present invention?
Refers to the core wire equivalent to JIS G 3523 Type 1 No. 1. Next, the effects of the present invention will be described in more detail based on Examples. [Example] As shown in Tables 1 and 2, an appropriate amount of water glass was mixed into coating materials with various compositions, and this was mixed into a 5mmφ×
A 700 mm mild steel core wire was coated and dried at a maximum temperature of 400°C to make welding rods A-1 to A-8 and B-1 to B-11. Root gap 1 ~ 1 with a V-bevel with a groove angle of 50° on a 20 mm thick aluminum killed steel plate using the above-mentioned test bar.
3 mm was taken, and downward welding was performed at a welding current of 220 A and a welding heat input of 18 KJ/cm. Thereafter, a 2 mm V-notched mechanical impact test piece was taken from 2 mm below the plate thickness surface on the final pass side and tested at -60°C. In the welding workability test, a steel plate (16 mm thick) coated with a 20 μm wash primer was placed in a horizontal fillet position.
The welding current was 230A and the rod operation ratio was 1.3. As for the judgment criteria, an impact value of 5 kgf-m or more at -60°C was considered good. In addition, ○ marks for welding workability are good, △
The mark means slightly defective, and the cross mark means defective.

【表】【table】

【表】【table】

〔発明の効果〕〔Effect of the invention〕

以上述べたごとく本発明の溶接棒は、被覆剤を
構成する配合成分の種類を特定すると共に各成分
の配合割合を特定範囲に設定することにより、従
来の溶接棒より安価で低温でのシヤルピーの衝撃
じん性の良好な溶接金属が得られ、かつビード形
状、ビード外観およびその他の溶接性能を満足
し、海洋構造物あるいはその他の構造物の安全性
に大きく寄与することができるものであり、産業
上の効果は極めて顕著なものがある。
As described above, the welding rod of the present invention is less expensive than conventional welding rods and has a high shear strength at low temperatures by specifying the types of compounded components that make up the coating material and setting the compounding ratio of each component within a specific range. It produces weld metal with good impact toughness, satisfies bead shape, bead appearance, and other welding performance, and can greatly contribute to the safety of marine structures and other structures, making it an industrial choice. The above effects are extremely remarkable.

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

第1図はSiO2含有率とTi、Si、SiC、Mg、Al
含有率の関係を示すグラフ、第2図は溶接金属の
vTrsと溶接金属中のSi量の関係を示すグラフで
ある。
Figure 1 shows SiO 2 content and Ti, Si, SiC, Mg, Al
A graph showing the relationship between content rates, Figure 2 is for weld metal.
2 is a graph showing the relationship between vTrs and the amount of Si in weld metal.

Claims (1)

【特許請求の範囲】[Claims] 1 チタン酸化物をTiO2に換算して13〜23重量
%、Ti、Si、SiC、Mg、Alの一種以上の合計を
0.1〜8重量%、硼素の酸化物または硼素の酸化
物の化合物をB2O3に換算して0.05〜2重量%、
MgCO3を4〜18重量%、金属弗化物0.1〜17重量
%、SiO21〜15重量%、MgO9〜22重量%、Mn1
〜10重量%、鉄粉10〜50重量%を含有し、かつ
SiO2含有率をY(重量%)、Ti+Si+SiC+Mg+
Alで計算される脱酸剤含有率をX(重量%)とし
たとき、5≦Y+2X≦16なる条件を満足し、更
にNi0.5〜6.5重量%を含む被覆剤に粘結剤を添加
し、鋼心線に塗装してなることを特徴とする低水
素系被覆アーク溶接棒。
1 Titanium oxide converted to TiO 2 13 to 23% by weight, the total of one or more of Ti, Si, SiC, Mg, and Al
0.1 to 8% by weight, 0.05 to 2% by weight of boron oxide or boron oxide compound converted to B2O3 ,
4-18 wt% MgCO3 , 0.1-17 wt% metal fluoride, 1-15 wt% SiO2 , 9-22 wt% MgO, Mn1
~10% by weight, containing 10-50% by weight of iron powder, and
SiO 2 content is Y (weight%), Ti + Si + SiC + Mg +
When the deoxidizer content calculated by Al is X (wt%), the following condition is satisfied: 5≦Y+2X≦16, and a binder is added to the coating material containing 0.5 to 6.5 wt% Ni. , a low hydrogen-based coated arc welding rod characterized by being made by coating a steel core wire.
JP29455985A 1985-12-27 1985-12-27 Low hydrogen type covered electrode Granted JPS62156097A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP29455985A JPS62156097A (en) 1985-12-27 1985-12-27 Low hydrogen type covered electrode

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP29455985A JPS62156097A (en) 1985-12-27 1985-12-27 Low hydrogen type covered electrode

Publications (2)

Publication Number Publication Date
JPS62156097A JPS62156097A (en) 1987-07-11
JPH0462837B2 true JPH0462837B2 (en) 1992-10-07

Family

ID=17809351

Family Applications (1)

Application Number Title Priority Date Filing Date
JP29455985A Granted JPS62156097A (en) 1985-12-27 1985-12-27 Low hydrogen type covered electrode

Country Status (1)

Country Link
JP (1) JPS62156097A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5560504B2 (en) * 2008-06-24 2014-07-30 ナショナル アカデミー オブ サイエンス オブ ウクライナ イー.オー. パトン エレクトリック ウェルディング インスティチュート Tungsten inert gas arc welding flux for steel
KR101637471B1 (en) * 2014-10-30 2016-07-07 현대종합금속 주식회사 Flux cored wire for Gas shielded arc welding

Also Published As

Publication number Publication date
JPS62156097A (en) 1987-07-11

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