JPH0253159B2 - - Google Patents
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- Publication number
- JPH0253159B2 JPH0253159B2 JP18076282A JP18076282A JPH0253159B2 JP H0253159 B2 JPH0253159 B2 JP H0253159B2 JP 18076282 A JP18076282 A JP 18076282A JP 18076282 A JP18076282 A JP 18076282A JP H0253159 B2 JPH0253159 B2 JP H0253159B2
- Authority
- JP
- Japan
- Prior art keywords
- welding
- welding rod
- steel
- weld metal
- strength
- 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
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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Cr−Mo鋼溶接用被覆アーク溶接棒に
関し、特に9%Cr鋼溶接用として優れた性能を
発揮する被覆アーク溶接棒に関するものである。
最近ボイラー等の加熱・加圧操業機器の設計に
当つては、熱効率や圧力効率の向上を期して操業
時の温度及び圧力を高めようとする動きがあり、
それに伴つて構成材料に対する耐酸化性、耐食性
及び高温強度等についても高度のものが要求され
るので、これらの要求を満たすものとして例えば
9Cr−2Mo鋼や9Cr−1Mo−Nb−V鋼等のCr−
Mo鋼が開発されている。
一方この様なCr−Mo鋼用の溶接材としては主
として9Cr−1Mo系溶接棒が使用されているが、
これらの溶接棒によつて得られる溶接部は高温強
度や長時間クリープ破断強度等が十分でなく、母
材に匹敵する継手性能を得ることができず、前述
の様な高温・高圧化の要請に応ずることができな
かつた。その理由の1つは、溶接金属中に析出す
る粗大フエライト相が溶接金属の強度、靭性及び
耐割れ性等を低下させる為と考えられている。そ
こで改善策として溶接材料中に多量のNiやMn等
のオーステナイト相安定化元素を含有させ、溶接
金属中の粗大フエライト相を減少させる方法も提
案されているが、過量のNiは長時間クリープ破
断強度を低下させ、また必要以上のNiやMnは溶
接金属の耐割れ性を低下させるので、目標とする
高性能の溶接継手を得ることはできない。
本発明者等は上記の様な事情に着目し、高温強
度や高温クリープ強度、更には耐割れ性等を損な
うことなく粗大フエライト相を減少し、母材に匹
敵する強度、靭性及び耐割れ性等を確保すること
のできる様なCr−Mo鋼溶接用被覆アーク溶接棒
を提供しようとして鋭意研究を進めてきた。本発
明はこうした研究の結果完成されたものであつ
て、その構成は、金属炭酸塩:30〜70%(重量
%:以下同じ)、金属弗化物:10〜30%、金属酸
化物:4〜25%を含有する被覆剤を溶接棒全重量
に対して20〜40%となる様に鋼心線外周に塗布し
てなり、且つ前記被覆剤及び/又は鋼心線中に
は、溶接棒全重量に対して炭素:0.04〜0.15%、
珪素:0.2〜1.6%、Mn:0.4〜1.6%、Cr:6.5〜13
%、Mo:0.7〜2.3%、N:0.01〜0.04%を含有さ
せる他、Ni:0.2〜1.5%、V:0.02〜0.25%、
Nb:0.02〜0.25%及びB:0.0005〜0.005%よりな
る群から選択される1種以上の元素を含有せし
め、且つV、Nb及びBの総和が0.4以下となる様
に調整し、あるいは更に次式により算出される
PFA値が4〜20となる様に調整したところに要旨
が存在する。
PFA値=(Si+V+Mo+Cr+Nb)/(Mn+Ni+N)(重
量比)
即ち本発明では、粗大フエライト相の析出抑制
効果とフエライト相安定化効果を有するSi、V、
Mo、Cr及びNbと、オーステナイト相安定化効
果を有するMn、Ni及びNを溶接材料中に夫々適
量含有せしめ、粗大フエライト相を微細化させる
と共に、溶接金属中に占めるフエライト量をコン
トロールし、それにより高温強度及び高温クリー
プ強度を母材並みに高めると共に、靭性の増大、
SR処理に対する軟化抵抗の増大、及び優れた溶
接作業性の確保等を一挙に達成することができ
る。
以下本発明における成分組成設定の理由を詳細
に説明する。
まず本発明において被覆剤中の金属炭酸塩、金
属弗化物及び金属酸化物の含有率及び被覆率を定
めた理由は次の通りである。
金属炭酸塩:30〜70%
30%未満では溶融スラグの粘度が低くなりすぎ
て溶接中のスラグが先行し易くなり溶接作業性が
悪化する他、凝固スラグの剥離性が悪化する等、
溶接作業性を満足できない。一方70%を越えると
溶融スラグの粘度が高くなりすぎ、スパツタが増
加すると共にビード外観も悪化する。
金属弗化物:10〜30%
10%未満では溶融スラグの粘度が高くなりすぎ
てビード外観が悪化し、一方30%を越えると溶融
スラグの粘度が低くなりすぎて溶接作業性が悪化
する等、何れの場合も満足な溶接作業性が得られ
なくなる。
金属酸化物:4〜25%
4%未満では溶接作業性が悪化すると共にビー
ド外観も著しく悪くなり、一方25%を越えると溶
融スラグの粘度が低くなつて凝固スラグの剥離性
が劣化する他スパツタ発生量も著しく増加する。
被覆率:20〜40%
被覆率とは溶接棒全重量に対する被覆剤の重量
%を意味し、20%未満では保護筒としての機能が
不十分になつてスパツタが増加したり、生成スラ
グ量の不足によつてビード外観が悪化し、一方40
%を越えるとスラグ量が多くなりすぎる為にスラ
グ巻込み等の欠陥が発生し易くなると共に、開先
幅の狭い溶接継手に適用した場合に運棒が困難に
なる。
次に上記溶接棒、即ち被覆剤及び鋼心線の何れ
かに含有させる必須元素について詳述する。
C:0.04〜0.15%
Cは溶接金属中に歩留つて粗大フエライト相の
析出を抑制する効果があり、溶接棒中に少なくと
も0.04%以上含有させなければならない。しかし
多すぎると溶接金属の耐割れ性が劣化するので
0.15%以下に抑えなければならない。
Si:0.2〜1.6%
溶接金属中の脱酸を主目的とするもので、溶接
棒中の含有率が0.2%未満では脱酸不足によつて
溶接金属中にブローホール等の気孔欠陥が発生し
易く、一方1.6%を越えると粗大フエライト相が
析出し易くなると共に溶接金属の靭性が低下す
る。
Mn:0.4〜1.6%
溶接金属の強度を高めるのに不可欠の成分であ
り、少なくとも0.4%含有させなければならない
が、1.6%を越えると溶接金属の微細フエライト
がなくなつて焼入硬化性が過大となり、耐割れ性
が悪化する。
Cr:6.5〜13%
溶接金属の耐酸化性、耐食性及び高温強度を高
めるのに不可欠の元素で、この種の成分系におけ
る主成分である。このCrの効果は溶接棒中に6.5
〜13%含有させることによつて有効に発揮され
る。
Mo:0.7〜2.3%
高温強度を高めると共に溶接金属の耐割れ性を
高める効果があり、0.4%以上、好ましくは0.7%
以上含有させなければならない。しかし多すぎる
と炭素当量を高めて溶接性を悪くするので2.3%
以下に抑える必要がある。
N:0.01〜0.04%
オーステナイト化安定元素の1つであり、かつ
旧オーステナイト結晶粒微細化作用があり、衝撃
値を向上させる。しかし0.01%以下の通常含有す
る量ではその効果がなく、逆に0.04%以上になる
と必要以上に強度を向上させ、衝撃値が低下す
る。かつまた上限値を越えると溶接金属中にブロ
ーホール等の気孔欠陥が発生し易くなるので0.04
%以下に止めるべきである。
Ni:0.2〜1.5%、V:0.02〜0.25%、Nb:0.02
〜0.25%及びB:0.0005〜0.005%の1種以上
これらの元素のうちV、Nb及びBは夫々単独
であるいは2種以上を組合せて含有させることに
より、前記Moの添加効果を相剰的に高める作用
を有するが、夫々下限未満ではその効果が有効に
発揮されず、殊にBの場合0.0005%未満で溶接金
属中への添加量をコントロールすることは実際上
極めて困難である。一方夫々上限を越えると逆に
溶接金属の靭性が低下すると共に溶接作業性も低
下する。これら3元素の総和が0.4%を越えると
衝撃強度が乏しくなる。尚Mo量が1.5〜2.3%で
ある場合はこれら3元素を併用しなくとも十分な
高温強度が得られるので、これら3元素は特に必
須元素としては定めなかつたが、Moが1.4%を越
えると粗大フエライト相の生成を生じ易くなるの
で、Niを0.2%以上含有させてMoの上記欠点を
補なう必要がある。しかしNiが多すぎると高温
強度及び高温クリープ強度が著しく低下すると共
に耐割れ性も損なわれるので1.5%以下に抑えな
ければならない。尚Niは単独で使用してもよく、
あるいはV、Nb及びBと共に併用することもで
きる。
本発明における必須の元素は以上の通りである
が、心線は上記元素の他Fe及び不可避不純物で
構成され、該不純物としては、S、P、O等が挙
げられる。
本発明溶接棒中に含まれる元素の種類及び好適
含有率は上記の通りであり、上記の要件を満足す
る限り本発明の目的は達成されるが、各元素の機
能を総合的に考慮し、溶接金属の高温強度、高温
クリープ強度、靭性、耐割れ性等を一層効果的に
高める為には、次式から算出されるPFA値を4〜
20の範囲に納めるのが極めて有効であるという結
論を得た。
PFA値=(Si+V+Mo+Cr+Nb)/(Mn+Ni+N)(重
量比)
即ちPFA値が4未満では微細フエライトの析出
量が少なくなつて溶着金属が硬くなりすぎるきら
いがあつて耐割れ性が不足気味になり、一方20を
越えると溶接金属中の粗大フエライト量が増加
し、高温強度及び高温クリープ強度が低下する。
尚上記各合金元素は鋼心線及び被覆剤のどちら
に含有させておいてもよいが、一例として主たる
合金元素であるCr及びMoの好ましい含有法を例
示すると、Crは鋼心線中に5〜12%(より一般
的には7〜9%)程度、被覆剤中に4〜0%(よ
り一般的には2〜0%)程度、またMoは鋼心線
中に0.4〜2%(より一般的には0.5〜1.5%)程
度、被覆剤中に2〜0%(より一般的には1.5〜
0%)程度含有させる方法である。この様な方法
を採用すれば、
鋼心線から100%添加する場合に比べて、結
果的に溶着金属中の元素量が同じであつても、
溶接中の棒焼けを軽減することができる(芯線
中にCrやMoを全量添加すると電気抵抗が増大
し、棒焼けを起こし易くなる)、
鋼心線として異なる含有率のものを多数準備
する必要がなく、心線の種類を統合できる、
心線中の合金成分量を減らした方が製造上有
利であり、安価に提供することができる、
等の効果が期待できる。反面、Cr等の場合、被
覆剤から多量添加すると溶接金属中で偏析を生じ
る恐れがあるので、被覆剤からのCrの添加率は
4%以下に抑えるのがよい。
本発明は概略以上の様に構成されており、被覆
剤及び心線中に含有させる合金元素の種類及び含
有率を特定することによつて、Cr−Mo鋼母材に
匹敵する物性を有する溶接金属を得ることがで
き、この種の特殊鋼を母材とする高温高圧反応設
備等の品質を大幅に高め得ることになつた。
次に実施例を挙げて本発明の構成及び作用効果
を具体的に説明する。
実施例
Cr−Mo鋼心線(5mm〓)の外周に被覆率が28
〜30%となる様に被覆剤を塗布し、第1表に示す
成分組成の被覆アーク溶接棒を製造した。得られ
た各溶接棒を用い、9Cr−1Mo鋼板を母材として
溶接実験を行ない第2表の結果を得た。尚溶接条
件は下記の通りとし、溶接終了後720℃で1時間
の歪取り焼鈍を行なつた後物性試験を行なつた。
〔溶接条件〕
使用電流:210アンペア
予熱パス間温度:200〜250℃
使用開先形状:第1図(溶接部内面側は同溶接棒
にて2層のバタリングを行なう)
溶接姿勢:下向き
The present invention relates to a coated arc welding rod for welding Cr-Mo steel, and particularly to a coated arc welding rod that exhibits excellent performance for welding 9% Cr steel. Recently, when designing boilers and other heating and pressurizing operating equipment, there has been a movement to increase the temperature and pressure during operation in order to improve thermal efficiency and pressure efficiency.
Along with this, a high degree of oxidation resistance, corrosion resistance, high temperature strength, etc. is required for the constituent materials.
Cr- such as 9Cr-2Mo steel and 9Cr-1Mo-Nb-V steel
Mo steel has been developed. On the other hand, 9Cr-1Mo welding rods are mainly used as welding materials for Cr-Mo steel.
The welds obtained with these welding rods do not have sufficient high-temperature strength or long-term creep rupture strength, making it impossible to obtain joint performance comparable to that of the base metal, and meeting the above-mentioned demands for higher temperatures and higher pressures. I was unable to respond. One of the reasons for this is thought to be that the coarse ferrite phase precipitated in the weld metal reduces the strength, toughness, crack resistance, etc. of the weld metal. Therefore, as an improvement measure, a method has been proposed in which a large amount of austenite phase stabilizing elements such as Ni and Mn is contained in the welding material to reduce the coarse ferrite phase in the weld metal, but excessive Ni causes long-term creep rupture. Since the strength is reduced, and more Ni and Mn than necessary reduce the cracking resistance of the weld metal, it is not possible to obtain the desired high-performance welded joint. The present inventors focused on the above-mentioned circumstances, and reduced the coarse ferrite phase without impairing high temperature strength, high temperature creep strength, or cracking resistance, and achieved strength, toughness, and cracking resistance comparable to that of the base material. We have been conducting intensive research in an attempt to provide a coated arc welding rod for welding Cr-Mo steel that can ensure the following. The present invention was completed as a result of such research, and its composition is: metal carbonate: 30-70% (weight %: the same hereinafter), metal fluoride: 10-30%, metal oxide: 4-70%. A coating material containing 25% of the total weight of the welding rod is applied to the outer periphery of the steel core wire in an amount of 20 to 40% based on the total weight of the welding rod, and the coating material and/or the steel core wire contains a Carbon by weight: 0.04-0.15%,
Silicon: 0.2-1.6%, Mn: 0.4-1.6%, Cr: 6.5-13
%, Mo: 0.7 to 2.3%, N: 0.01 to 0.04%, Ni: 0.2 to 1.5%, V: 0.02 to 0.25%,
Contain one or more elements selected from the group consisting of Nb: 0.02 to 0.25% and B: 0.0005 to 0.005%, and adjust so that the sum of V, Nb and B is 0.4 or less, or further Calculated by the formula
The gist lies in adjusting the PFA value to be between 4 and 20. P FA value = (Si + V + Mo + Cr + Nb) / (Mn + Ni + N) (weight ratio) In other words, in the present invention, Si, V, which has the effect of suppressing the precipitation of the coarse ferrite phase and the effect of stabilizing the ferrite phase,
Mo, Cr, and Nb, and Mn, Ni, and N, which have austenite phase stabilizing effects, are contained in appropriate amounts in the welding material to refine the coarse ferrite phase and control the amount of ferrite in the weld metal. In addition to increasing high-temperature strength and high-temperature creep strength to the same level as the base metal, it also increases toughness.
It is possible to increase the softening resistance against SR treatment and ensure excellent welding workability all at once. The reasons for setting the component composition in the present invention will be explained in detail below. First, the reason why the content and coverage of metal carbonate, metal fluoride, and metal oxide in the coating material are determined in the present invention is as follows. Metal carbonate: 30-70% If it is less than 30%, the viscosity of the molten slag becomes too low and the slag during welding tends to precede it, resulting in poor welding workability, as well as poor removability of solidified slag, etc.
Welding workability cannot be satisfied. On the other hand, if it exceeds 70%, the viscosity of the molten slag becomes too high, spatter increases and the bead appearance deteriorates. Metal fluoride: 10-30% If it is less than 10%, the viscosity of the molten slag becomes too high and the appearance of the bead deteriorates, while if it exceeds 30%, the viscosity of the molten slag becomes too low and welding workability deteriorates, etc. In either case, satisfactory welding workability cannot be obtained. Metal oxide: 4 to 25% If it is less than 4%, welding workability deteriorates and the appearance of the bead becomes significantly worse. On the other hand, if it exceeds 25%, the viscosity of the molten slag becomes low and the removability of the solidified slag deteriorates, as well as spatters. The amount generated also increases significantly. Coverage rate: 20 to 40% Coverage rate means the weight percent of the coating material to the total weight of the welding rod. If it is less than 20%, the function as a protective tube will be insufficient, resulting in increased spatter, and the amount of slag generated will be reduced. The bead appearance worsens due to the deficiency, while 40
%, the amount of slag becomes too large, which tends to cause defects such as slag entrainment, and makes rod handling difficult when applied to welded joints with narrow groove widths. Next, the essential elements to be contained in the above-mentioned welding rod, that is, either the coating material or the steel core wire, will be explained in detail. C: 0.04-0.15% C is present in the weld metal and has the effect of suppressing the precipitation of coarse ferrite phase, and must be contained in the welding rod at least 0.04%. However, if it is too much, the cracking resistance of the weld metal will deteriorate.
Must be kept below 0.15%. Si: 0.2-1.6% The main purpose is to deoxidize the weld metal; if the content in the welding rod is less than 0.2%, pore defects such as blowholes will occur in the weld metal due to insufficient deoxidation. On the other hand, if it exceeds 1.6%, coarse ferrite phase tends to precipitate and the toughness of the weld metal decreases. Mn: 0.4-1.6% This is an essential component to increase the strength of weld metal, and it must be contained at least 0.4%, but if it exceeds 1.6%, the fine ferrite in the weld metal will disappear and the quench hardenability will be excessive. As a result, cracking resistance deteriorates. Cr: 6.5-13% This is an essential element for increasing the oxidation resistance, corrosion resistance, and high-temperature strength of weld metal, and is the main component in this type of component system. The effect of this Cr is 6.5 in the welding rod.
It is effectively exhibited by containing ~13%. Mo: 0.7-2.3% has the effect of increasing high temperature strength and cracking resistance of weld metal, 0.4% or more, preferably 0.7%
or more must be contained. However, if it is too large, the carbon equivalent will increase and weldability will deteriorate, so 2.3%
It is necessary to keep it below. N: 0.01 to 0.04% N is one of the stable elements for austenitization, has the effect of refining prior austenite crystal grains, and improves impact value. However, if the content is less than 0.01%, it will not have this effect, and if it is more than 0.04%, the strength will be increased more than necessary and the impact value will be lowered. Moreover, if the upper limit is exceeded, pore defects such as blowholes are likely to occur in the weld metal, so 0.04
It should be kept below %. Ni: 0.2-1.5%, V: 0.02-0.25%, Nb: 0.02
~0.25% and B: 0.0005~0.005% of one or more of these elements. By containing V, Nb, and B alone or in combination of two or more, the effect of adding Mo can be mutually enhanced. However, the effect is not effectively exhibited below the respective lower limits, and in the case of B in particular, it is actually extremely difficult to control the amount added to the weld metal at less than 0.0005%. On the other hand, if the respective upper limits are exceeded, the toughness of the weld metal and welding workability are reduced. When the sum of these three elements exceeds 0.4%, impact strength becomes poor. When the Mo content is 1.5 to 2.3%, sufficient high-temperature strength can be obtained without using these three elements together, so these three elements were not specified as essential elements, but when Mo exceeds 1.4%, Since coarse ferrite phase tends to occur, it is necessary to contain 0.2% or more of Ni to compensate for the above-mentioned drawbacks of Mo. However, if the Ni content is too large, the high temperature strength and high temperature creep strength will be significantly reduced, and the cracking resistance will also be impaired, so it must be kept at 1.5% or less. In addition, Ni may be used alone,
Alternatively, it can be used in combination with V, Nb and B. The essential elements in the present invention are as described above, and the core wire is composed of Fe and unavoidable impurities in addition to the above elements, and examples of the impurities include S, P, O, and the like. The types and preferred content of the elements contained in the welding rod of the present invention are as described above, and as long as the above requirements are satisfied, the purpose of the present invention is achieved. In order to more effectively increase the high-temperature strength, high-temperature creep strength, toughness, cracking resistance, etc. of weld metal, the P FA value calculated from the following formula should be set to 4 to 4.
We concluded that it is extremely effective to keep it within the range of 20. P FA value = (Si + V + Mo + Cr + Nb) / (Mn + Ni + N) (weight ratio) In other words, if the P FA value is less than 4, the amount of fine ferrite precipitated will be small and the weld metal will tend to become too hard, resulting in insufficient cracking resistance. On the other hand, when it exceeds 20, the amount of coarse ferrite in the weld metal increases, and the high temperature strength and high temperature creep strength decrease. Each of the above-mentioned alloying elements may be contained in either the steel core wire or the coating material, but as an example, a preferred method of containing Cr and Mo, which are the main alloying elements, is as follows. ~12% (more generally 7 to 9%), approximately 4 to 0% (more generally 2 to 0%) in the coating material, and 0.4 to 2% (more generally 2 to 0%) in the steel core wire. 2 to 0% (more generally 1.5 to 1.5%) in the coating.
This is a method of containing about 0%). If such a method is adopted, compared to adding 100% from the steel core wire, even if the amount of elements in the weld metal is the same,
It is possible to reduce stick burn during welding (adding all Cr or Mo to the core wire increases the electrical resistance, making stick burn more likely to occur), and it is necessary to prepare a large number of steel core wires with different contents. The following effects can be expected: it is possible to integrate the types of core wires, it is advantageous in manufacturing to reduce the amount of alloy components in the core wires, and it can be provided at low cost. On the other hand, in the case of Cr, etc., if a large amount is added from the coating material, segregation may occur in the weld metal, so the addition rate of Cr from the coating material is preferably suppressed to 4% or less. The present invention is roughly constructed as described above, and by specifying the type and content of alloying elements contained in the coating and the core wire, welding that has physical properties comparable to those of the Cr-Mo steel base material can be achieved. It has become possible to obtain metals and greatly improve the quality of high-temperature, high-pressure reaction equipment that uses this type of special steel as a base material. Next, the configuration and effects of the present invention will be specifically explained with reference to Examples. Example: Coverage ratio is 28 on the outer periphery of Cr-Mo steel core wire (5 mm〓)
A coating agent was applied to the coating material to give a coating concentration of ~30%, and coated arc welding rods having the composition shown in Table 1 were manufactured. Using each of the obtained welding rods, a welding experiment was conducted using a 9Cr-1Mo steel plate as a base material, and the results shown in Table 2 were obtained. The welding conditions were as follows, and after welding, strain relief annealing was performed at 720°C for 1 hour, and then physical property tests were conducted. [Welding conditions] Current used: 210 amperes Temperature between preheating passes: 200 to 250°C Groove shape used: Fig. 1 (Two layers of buttering are performed with the same welding rod on the inner side of the welding part) Welding position: downward
【表】【table】
【表】【table】
【表】
第1、2表からも明らかな様に、本発明の要件
を満たす溶接棒(No.1〜7)を用いて得た溶接部
は、室温強度、高温強度、伸び及び衝撃強度の何
れにおいても、従来棒や比較棒に比べて卓越した
性能を有している。このうち特にNo.2及び3の溶
接棒はMo量を相対的に多くした実施例であり、
この場合は選択元素としてNiを適量含有させる
ことによつて靭性を十分に高めることができる。
またNo.1、4〜7の溶接棒はMo量を比較的低レ
ベルに抑えたもので、この場合は選択元素として
Nb、V及びBの1種以上を含有させることによ
つて、高温強度や衝撃値等を十分に高めることが
できる。
これに対し従来棒(No.8、9)は高温強度及び
衝撃値共に不十分であり、また比較棒10、11は
PFA値が好適範囲を外れ、比較棒12はV及びB量
が多すぎる為、何れも衝撃値が極めて低い。
第2図は、第1表の溶接棒No.2(Mo含有率が
比較的高いもの)をベース組成とし、Ni量を変
えた場合の溶接部のシヤルピー衝撃値に与える影
響を調べた実験グラフである。この図より、Ni
量が0.2%未満ではそれ程の靭性向上効果は認め
られないが、これを越えると靭性は急激に向上
し、0.8%付近で飽和状態に達することが分かる。
そして1.5%を越えると靭性はむしろ低下傾向を
示す。従つてNiの効果を有効に発揮させる為に
は、その含有量を0.2〜1.5%、より好ましくは0.4
〜0.8%の範囲にすべきであることが理解される。
また第3図は、溶接棒No.2を用いて得た溶接金
属のクリープ破断試験結果を示したものである
が、併記する母材の試験結果と比較すれば明らか
である様に、母材と同程度以上の高温クリープ強
度を示している。[Table] As is clear from Tables 1 and 2, welds obtained using welding rods (Nos. 1 to 7) that meet the requirements of the present invention have low room temperature strength, high temperature strength, elongation, and impact strength. In both cases, it has superior performance compared to conventional rods and comparison rods. Among these, welding rods No. 2 and 3 in particular are examples in which the amount of Mo is relatively increased,
In this case, the toughness can be sufficiently increased by containing an appropriate amount of Ni as a selective element.
In addition, welding rods No. 1, 4 to 7 have a relatively low amount of Mo, and in this case, as the selected element,
By containing one or more of Nb, V, and B, high temperature strength, impact value, etc. can be sufficiently increased. On the other hand, the conventional bars (No. 8 and 9) are insufficient in both high temperature strength and impact value, and the comparative bars 10 and 11 are
The P FA value is out of the preferred range, and comparison bar 12 has too much V and B, so both have extremely low impact values. Figure 2 is an experimental graph that uses welding rod No. 2 in Table 1 (relatively high Mo content) as the base composition, and investigates the effect of varying the amount of Ni on the shear py impact value of the weld. It is. From this figure, Ni
It can be seen that when the amount is less than 0.2%, no significant toughness improvement effect is observed, but when this amount is exceeded, the toughness rapidly improves and reaches a saturation state at around 0.8%.
If the content exceeds 1.5%, the toughness tends to decrease. Therefore, in order to effectively exhibit the effect of Ni, the content should be 0.2 to 1.5%, more preferably 0.4%.
It is understood that it should be in the range ~0.8%. Fig. 3 shows the results of the creep rupture test of weld metal obtained using welding rod No. 2. It shows high-temperature creep strength comparable to or higher than that of
第1図は溶接実験で用いた開先形状を示す図、
第2図は溶接棒中のNi量と溶接金属の衝撃値の
関係を示すグラフ、第3図はクリープ破断試験結
果を示すグラフである。
Figure 1 shows the groove shape used in the welding experiment.
FIG. 2 is a graph showing the relationship between the amount of Ni in the welding rod and the impact value of the weld metal, and FIG. 3 is a graph showing the results of the creep rupture test.
Claims (1)
金属弗化物:10〜30%、金属酸化物:4〜25%を
含有する被覆剤を溶接棒全重量に対して20〜40%
となる様に鋼心線外周に塗布してなり、且つ前記
被覆剤及び/又は鋼心線中には、溶接棒全重量に
対して炭素:0.04〜0.15%、珪素:0.2〜1.6%、
Mn:0.4〜1.6%、Cr:6.5〜13%及びMo:0.7〜
2.3%、N:0.01〜0.04%を含有させる他、Ni:
0.2〜1.5%、V:0.02〜0.25%、Nb:0.02〜0.25%
及びB:0.0005〜0.005%よりなる群から選択さ
れる少なくとも1種以上の元素を含有せしめ、且
つV、Nb及びBの総和が0.4以下となる様に調整
したことを特徴とするCr−Mo鋼溶接用被覆アー
ク溶接棒。 2 金属炭酸塩:30〜70%(重量%:以下同じ)、
金属弗化物:10〜30%、金属酸化物:4〜25%を
含有する被覆剤を溶接棒全重量に対して20〜40%
となる様に鋼心線外周に塗布してなり、且つ前記
被覆剤及び/又は鋼心線中には、溶接棒全重量に
対して炭素:0.04〜0.15%、珪素:0.2〜1.6%、
Mn:0.4〜1.6%、Cr:6.5〜13%及びMo:0.7〜
2.3%、N:0.01〜0.04%を含有させる他、Ni:
0.2〜1.5%、V:0.02〜0.25%、Nb:0.02〜0.25%
及びB:0.0005〜0.005%よりなる群から選択さ
れる少なくとも1種以上の元素を含有せしめ、且
つV、Nb及びBの総和が0.4%以下となる様に調
整する他、次式より算出されるPFA値を4〜20に
してなることを特徴とするCr−Mo鋼溶接用被覆
アーク溶接棒。 PFA値=(Si+V+Mo+Cr+Nb)/(Mn+Ni+N)(重
量比)[Claims] 1. Metal carbonate: 30 to 70% (weight %: the same below),
Coating material containing metal fluoride: 10-30%, metal oxide: 4-25%, based on the total weight of the welding rod, 20-40%
The coating agent and/or the steel core wire contain carbon: 0.04 to 0.15%, silicon: 0.2 to 1.6%, based on the total weight of the welding rod.
Mn: 0.4~1.6%, Cr: 6.5~13% and Mo: 0.7~
In addition to containing 2.3%, N: 0.01 to 0.04%, Ni:
0.2-1.5%, V: 0.02-0.25%, Nb: 0.02-0.25%
and B: Cr-Mo steel containing at least one element selected from the group consisting of 0.0005 to 0.005%, and adjusted so that the sum of V, Nb and B is 0.4 or less. Covered arc welding rod for welding. 2 Metal carbonate: 30 to 70% (weight%: same below),
Coating material containing metal fluoride: 10-30%, metal oxide: 4-25%, based on the total weight of the welding rod, 20-40%
The coating agent and/or the steel core wire contain carbon: 0.04 to 0.15%, silicon: 0.2 to 1.6%, based on the total weight of the welding rod.
Mn: 0.4~1.6%, Cr: 6.5~13% and Mo: 0.7~
In addition to containing 2.3%, N: 0.01 to 0.04%, Ni:
0.2-1.5%, V: 0.02-0.25%, Nb: 0.02-0.25%
and B: contains at least one element selected from the group consisting of 0.0005 to 0.005%, and is adjusted so that the sum of V, Nb, and B is 0.4% or less, and is calculated from the following formula. A coated arc welding rod for welding Cr-Mo steel, characterized by having a P FA value of 4 to 20. P FA value = (Si + V + Mo + Cr + Nb) / (Mn + Ni + N) (weight ratio)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18076282A JPS5970494A (en) | 1982-10-14 | 1982-10-14 | Coated electrode for welding cr-mo steel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP18076282A JPS5970494A (en) | 1982-10-14 | 1982-10-14 | Coated electrode for welding cr-mo steel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5970494A JPS5970494A (en) | 1984-04-20 |
| JPH0253159B2 true JPH0253159B2 (en) | 1990-11-15 |
Family
ID=16088875
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP18076282A Granted JPS5970494A (en) | 1982-10-14 | 1982-10-14 | Coated electrode for welding cr-mo steel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5970494A (en) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS61266199A (en) * | 1985-05-17 | 1986-11-25 | Kobe Steel Ltd | Coated electrode for welding cr-mo steel |
| JPH069756B2 (en) * | 1986-03-20 | 1994-02-09 | 新日本製鐵株式会社 | Low-hydrogen coated arc welding rod |
| FR2946554B1 (en) * | 2009-06-10 | 2012-06-08 | Air Liquide Welding France | STAINLESS STEEL COATED ELECTRODE AND LITHIUM COATING |
| CN102357750B (en) * | 2011-09-21 | 2013-05-22 | 于风福 | A flux-cored welding wire surfacing material |
| CN105014261B (en) * | 2015-07-30 | 2017-08-04 | 武汉铁锚焊接材料股份有限公司 | A kind of chrome-molybdenum steel seamless metal powder core type flux-cored wire |
-
1982
- 1982-10-14 JP JP18076282A patent/JPS5970494A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5970494A (en) | 1984-04-20 |
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