JPS5922633B2 - Low hydrogen coated arc welding rod - Google Patents
Low hydrogen coated arc welding rodInfo
- Publication number
- JPS5922633B2 JPS5922633B2 JP15741580A JP15741580A JPS5922633B2 JP S5922633 B2 JPS5922633 B2 JP S5922633B2 JP 15741580 A JP15741580 A JP 15741580A JP 15741580 A JP15741580 A JP 15741580A JP S5922633 B2 JPS5922633 B2 JP S5922633B2
- Authority
- JP
- Japan
- Prior art keywords
- less
- welding rod
- weight
- powder
- coated arc
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired
Links
- 238000003466 welding Methods 0.000 title claims description 48
- 229910052739 hydrogen Inorganic materials 0.000 title claims description 16
- 239000001257 hydrogen Substances 0.000 title claims description 16
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 title claims description 8
- 229910052751 metal Inorganic materials 0.000 claims description 55
- 239000002184 metal Substances 0.000 claims description 53
- 239000000843 powder Substances 0.000 claims description 53
- 239000002245 particle Substances 0.000 claims description 42
- 239000011248 coating agent Substances 0.000 claims description 31
- 238000000576 coating method Methods 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 27
- 229910045601 alloy Inorganic materials 0.000 claims description 21
- 239000000956 alloy Substances 0.000 claims description 21
- 239000003795 chemical substances by application Substances 0.000 claims description 14
- 229910000831 Steel Inorganic materials 0.000 claims description 13
- 239000010959 steel Substances 0.000 claims description 13
- 239000002994 raw material Substances 0.000 claims description 8
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 4
- 229910052750 molybdenum Inorganic materials 0.000 claims description 2
- 238000005204 segregation Methods 0.000 description 25
- 239000011162 core material Substances 0.000 description 16
- 229910052799 carbon Inorganic materials 0.000 description 12
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 11
- 239000011362 coarse particle Substances 0.000 description 9
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 8
- 239000000203 mixture Substances 0.000 description 8
- 229910052804 chromium Inorganic materials 0.000 description 7
- 230000007423 decrease Effects 0.000 description 7
- 230000000704 physical effect Effects 0.000 description 7
- 239000002893 slag Substances 0.000 description 7
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000012360 testing method Methods 0.000 description 6
- 229910001634 calcium fluoride Inorganic materials 0.000 description 5
- 150000002739 metals Chemical class 0.000 description 5
- 229910052759 nickel Inorganic materials 0.000 description 5
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N titanium dioxide Inorganic materials O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 5
- 238000002474 experimental method Methods 0.000 description 4
- 239000003381 stabilizer Substances 0.000 description 4
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 3
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 3
- 239000011230 binding agent Substances 0.000 description 3
- 239000010419 fine particle Substances 0.000 description 3
- 229910052748 manganese Inorganic materials 0.000 description 3
- 239000011572 manganese Substances 0.000 description 3
- 235000019353 potassium silicate Nutrition 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- 229910021532 Calcite Inorganic materials 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- 229910002551 Fe-Mn Inorganic materials 0.000 description 2
- 229910017082 Fe-Si Inorganic materials 0.000 description 2
- 229910017133 Fe—Si Inorganic materials 0.000 description 2
- 239000004111 Potassium silicate Substances 0.000 description 2
- 229920002472 Starch Polymers 0.000 description 2
- 238000009825 accumulation Methods 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 229910052796 boron Inorganic materials 0.000 description 2
- 229910001748 carbonate mineral Inorganic materials 0.000 description 2
- 238000005336 cracking Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 238000004453 electron probe microanalysis Methods 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000012535 impurity Substances 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052758 niobium Inorganic materials 0.000 description 2
- 230000035515 penetration Effects 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- NNHHDJVEYQHLHG-UHFFFAOYSA-N potassium silicate Chemical compound [K+].[K+].[O-][Si]([O-])=O NNHHDJVEYQHLHG-UHFFFAOYSA-N 0.000 description 2
- 229910052913 potassium silicate Inorganic materials 0.000 description 2
- 238000011160 research Methods 0.000 description 2
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 2
- 238000007711 solidification Methods 0.000 description 2
- 230000008023 solidification Effects 0.000 description 2
- 239000008107 starch Substances 0.000 description 2
- 235000019698 starch Nutrition 0.000 description 2
- 230000009466 transformation Effects 0.000 description 2
- 230000007704 transition Effects 0.000 description 2
- 229910000975 Carbon steel Inorganic materials 0.000 description 1
- 241001391944 Commicarpus scandens Species 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910002593 Fe-Ti Inorganic materials 0.000 description 1
- 229910001182 Mo alloy Inorganic materials 0.000 description 1
- KKCBUQHMOMHUOY-UHFFFAOYSA-N Na2O Inorganic materials [O-2].[Na+].[Na+] KKCBUQHMOMHUOY-UHFFFAOYSA-N 0.000 description 1
- 239000004115 Sodium Silicate Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 238000005275 alloying Methods 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 235000010216 calcium carbonate Nutrition 0.000 description 1
- 150000001721 carbon Chemical class 0.000 description 1
- 229910002091 carbon monoxide Inorganic materials 0.000 description 1
- 239000010962 carbon steel Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 229910001610 cryolite Inorganic materials 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 150000002222 fluorine compounds Chemical class 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- -1 illuminite Inorganic materials 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000006249 magnetic particle Substances 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- NOTVAPJNGZMVSD-UHFFFAOYSA-N potassium monoxide Inorganic materials [K]O[K] NOTVAPJNGZMVSD-UHFFFAOYSA-N 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 229910052604 silicate mineral Inorganic materials 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 229910052911 sodium silicate Inorganic materials 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
- 238000005493 welding type Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
Landscapes
- Nonmetallic Welding Materials (AREA)
Description
【発明の詳細な説明】
本発明は低水素系被覆アーク溶接棒に関し、特に低温靭
性と引張り強さの良い溶接金属を与える低水素系被覆ア
ーク溶接棒に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a low-hydrogen coated arc welding rod, and more particularly to a low-hydrogen coated arc welding rod that provides a weld metal with good low-temperature toughness and tensile strength.
低温用鋼や50に9f/m4級以上の高張力鋼等の溶接
に使用される被覆アーク溶接棒の被覆には、溶接金属に
対して所定の強度を与える為にMn、Cr及びMo等を
、また靭性向上の為にNi等を、夫々金属粉や合金粉の
形で含有させるのが通例である。しかしこれらの被覆ア
ーク溶接棒を用いた場合でも、溶接金属の切欠靭性は不
十分であり、また高強度を得る為に多量の合金元素を添
加すると、溶接金属が硬化して切欠靭性は更に低下し、
且つ合金成分が十分に拡散せずに凝固して偏析が起こり
強度の均一性が阻害される。例えば参考写真1は従来の
被覆アーク溶接棒を用いて得た溶着金属中のNiの偏析
状態を示す断面マクロ写真で、○で囲んだ部分に偏析が
みられる。The coating of coated arc welding rods used for welding low-temperature steel and high-tensile steel of grade 50 to 9 f/m4 or higher contains Mn, Cr, Mo, etc. in order to give a specified strength to the weld metal. Furthermore, in order to improve toughness, it is customary to contain Ni or the like in the form of metal powder or alloy powder, respectively. However, even when these coated arc welding rods are used, the notch toughness of the weld metal is insufficient, and when large amounts of alloying elements are added to obtain high strength, the weld metal hardens and the notch toughness further deteriorates. death,
In addition, the alloy components solidify without being sufficiently diffused, causing segregation and impairing the uniformity of strength. For example, reference photo 1 is a cross-sectional macro photo showing the state of Ni segregation in the deposited metal obtained using a conventional coated arc welding rod, and segregation is seen in the circled area.
参考写真2は偏析部分の50倍拡大写真を示す。また第
1図はEPMAによるNiの分析結果であり、マクロ偏
析の状況が確認できる。但し、EPMAの測定条件はA
CC、電圧:20KV、試料電流:0.05μAlチャ
ートスピード:20Rm/分、試料スピード:50μm
/分である。上記マクロ偏析による溶接金属の物性低下
は、特に低水素系被覆アーク溶接棒を使用した場合に端
的に現われる。しかしてこの種の溶接棒を用いた溶接金
属は衝撃値が高いという特長を有しており、Niの添加
効果が最も発揮される溶接棒であるから、マクロ偏析に
よる上記物性の低下が特に問題になり易く、また磁粉探
傷試験において偏析に沿つた模様も観察される。本発明
者等は前述の様な事情に着目し、まずマクロ偏析の発生
原因を究明すべく実験を行なつた。Reference photo 2 shows a 50 times enlarged photo of the segregated area. Moreover, FIG. 1 shows the analysis results of Ni by EPMA, and the state of macro segregation can be confirmed. However, the measurement conditions of EPMA are A
CC, voltage: 20KV, sample current: 0.05μAl chart speed: 20Rm/min, sample speed: 50μm
/minute. The deterioration in the physical properties of weld metal due to the above-mentioned macro-segregation is particularly apparent when a low-hydrogen coated arc welding rod is used. However, the weld metal using this type of welding rod has a high impact value, and since it is the welding rod that exhibits the effect of Ni addition most, the deterioration of the above physical properties due to macro segregation is a particular problem. Also, patterns along the lines of segregation are observed in magnetic particle testing. The inventors of the present invention paid attention to the above-mentioned circumstances and conducted experiments to first investigate the cause of macro segregation.
その結果、被覆剤中に配合される金属粉の合金粉の粒度
がマクロ偏析と密接な関係を有していることが確認され
る。即ち溶接工程で被覆剤から溶融プール内に移行した
金属粉や合金粉は、微細粒子であればアークカによつで
溶融金属内へー様に分散する。ところが粗粒物では一様
に分散する前に凝固が完了しマクロ偏析となつて現われ
、アーク力の弱い低水素系被覆アーク溶接棒を使用した
場合にはその傾向が箸しくなる。そこで被覆剤中に配合
する金属粉や合金粉を極力微細にしてやればマクロ偏析
を抑制できるであろうと考え、その線に沿つて鋭意研究
の結果本発明に到達した。即ち本発明に係る低水素系被
覆アーク溶接棒とは、脱酸剤、スラグ生成剤及びアーク
安定剤を含有すると共に、CacO3,MgcO3及び
BacO3よりなる群から選択される1種以上の炭酸塩
を合計で25〜55%(重量(fl):以下同じ)、C
aF2を2〜30%、金属粉及び/又は合金粉を15%
以下並びに固着剤を主成分として含有する被覆剤を鋼心
線外周に途布してなる低水素系被覆アーク溶接棒におい
て、金属粉及び/又は合金粉を除く上記被覆剤原料の粒
度を、296μ以下で且つ74μ以下のものが25(f
)以下となる様に調整すると共に、金属粉及び/又は合
金粉の粒度を、149μ以上のものが20q6以下とな
る様に調整したところに要旨が存在する。本発明者等は
、被覆剤中に配合するNi,Cr及びMOの粒度がミク
ロ偏析と密接な関係を有しているという知見から、これ
らの関係を定量的に確認すべく実験を行なつた。As a result, it was confirmed that the particle size of the alloy powder of the metal powder mixed in the coating material has a close relationship with macro segregation. That is, if the metal powder or alloy powder transferred from the coating material into the molten pool during the welding process is a fine particle, it will be dispersed into the molten metal by the arc force. However, in the case of coarse particles, solidification is completed before they are uniformly dispersed, and macro segregation appears, and this tendency becomes worse when a low-hydrogen coated arc welding rod with weak arc force is used. Therefore, we thought that macro segregation could be suppressed by making the metal powder or alloy powder mixed in the coating material as fine as possible, and as a result of intensive research along this line, we arrived at the present invention. That is, the low hydrogen-based coated arc welding rod according to the present invention contains a deoxidizing agent, a slag forming agent, and an arc stabilizer, and also contains one or more carbonates selected from the group consisting of CacO3, MgcO3, and BacO3. 25 to 55% in total (weight (fl): same below), C
2-30% aF2, 15% metal powder and/or alloy powder
In a low-hydrogen coated arc welding rod in which a coating material containing a binder as a main component is distributed around the outer periphery of a steel core wire, the particle size of the coating material raw material excluding metal powder and/or alloy powder is 296 μm. Those below and 74μ or less are 25(f
), and the particle size of the metal powder and/or alloy powder is adjusted so that the particle size of 149μ or more becomes 20q6 or less. Based on the knowledge that the particle sizes of Ni, Cr, and MO contained in coating materials have a close relationship with microsegregation, the present inventors conducted experiments to quantitatively confirm these relationships. .
即ちCaCO3:45%、CaF2:18%、Si含有
率45%のFe一Si:10%、Mn:3q6及びTi
O2:3%からなる低水素系被覆剤を基本組成とし、こ
れに粒度構成の異なるNi粉を0.5〜16q6添加し
た後粘結剤として水ガラスを加え、これを鋼心線(5.
0wmφ)に塗布し400〜450℃で乾燥して供試棒
とした。この試供棒を用いて板厚100種のSM5O材
(V開先6開先角度:30度、ルートギヤツプ:10r
m)に、電流220Aで下向溶接した。得られた溶接金
属から5個の試験片を切り出して研磨し、50倍に拡大
して各断面における偏析の個数を調べた。また上記と同
様の方法で、Cr粉を1〜4.5%含有する供試棒及び
MO合金粉をMO換算で0.5〜3%含有する供試棒を
作製し、同様に偏析の個数を調べた。各試験片の平均偏
析個数は第2図に示す通りである。第2図からも明らか
な様に、被覆剤中の金属粉含有量が少ない場合は、金属
粉の粒度に関係なく偏析個数は極めて少ない。That is, CaCO3: 45%, CaF2: 18%, Si content of 45% Fe-Si: 10%, Mn: 3q6 and Ti
The basic composition is a low hydrogen coating agent consisting of 3% O2, to which 0.5 to 16q6 of Ni powder with different particle size composition is added, water glass is added as a binder, and this is made into a steel core wire (5.
0wmφ) and dried at 400 to 450°C to obtain a test bar. Using this sample rod, we used SM5O material of 100 different thicknesses (6 V grooves, groove angle: 30 degrees, root gap: 10r).
m) was welded downward at a current of 220A. Five test pieces were cut out from the obtained weld metal, polished, and enlarged 50 times to examine the number of segregations in each cross section. In addition, test bars containing 1 to 4.5% of Cr powder and test bars containing 0.5 to 3% of MO alloy powder in terms of MO were prepared in the same manner as above, and similarly the number of segregation I looked into it. The average number of segregated pieces of each test piece is as shown in FIG. As is clear from FIG. 2, when the metal powder content in the coating material is small, the number of segregated particles is extremely small regardless of the particle size of the metal powder.
また金属粉の含有量が多くなると、金属粉の粒度を調整
しても偏析を抑制できない。しかしNi,Cr及びMO
粉中に占める149μ以上の粗粒物の割合と偏析個数の
間には明らから相関々係がみられ、該粗粒物の割合を2
0%以下にすることによつて偏析個数を大幅に減するこ
とができる。CacO3,MgcO3及びBacO3は
何れも同効物質であり、溶接中に分解してCOやCO2
を発生しシールド効果を発揮する。Moreover, when the content of metal powder increases, segregation cannot be suppressed even if the particle size of the metal powder is adjusted. However, Ni, Cr and MO
There is a clear correlation between the proportion of coarse particles of 149μ or more in the powder and the number of segregated particles, and when the proportion of coarse particles is 2
By reducing the amount to 0% or less, the number of segregated particles can be significantly reduced. CacO3, MgcO3 and BacO3 are all equivalent substances and decompose during welding to produce CO and CO2.
occurs and exerts a shielding effect.
従つて十分なシールド効果を得る為には、上記炭酸塩の
1種以上を25%以上配合する必要がある。但し多すぎ
ると溶込みが深くなると共にスパツタが多発し易くなる
ので55%以下に止めねばならない。尚これらの炭酸塩
は同時にアーク安定剤やスラグ生成剤としての作用も発
揮する。CaF2はスラグ生成剤であつて溶融スラグの
流動性及び耐ピツト性を改善するのに不可欠の成分で、
少なくとも2#)以上含有させる必要がある。Therefore, in order to obtain a sufficient shielding effect, it is necessary to mix at least 25% of one or more of the above carbonates. However, if it is too large, the penetration becomes deep and spatter tends to occur frequently, so it must be kept at 55% or less. These carbonates also act as arc stabilizers and slag forming agents. CaF2 is a slag forming agent and is an essential component for improving the fluidity and pitting resistance of molten slag.
It is necessary to contain at least 2#) or more.
しかし多すぎるとアークが不安定になるので30%以下
に止めるべきである。欠に金属粉としては、前述の如く
Cr,MO及びNi等が挙げられ、これらは以下に示す
如く溶接金属の物理的性質を高める作用がある。However, if it is too large, the arc becomes unstable, so it should be kept at 30% or less. As mentioned above, examples of metal powder include Cr, MO, Ni, etc., and these have the effect of improving the physical properties of the weld metal as shown below.
しかし多すぎると物性面でかえつて障害が現われると共
に偏析が起こり易くなる。即ちCrは溶接金属の強度向
上に寄与するが、3.5%を越えると偏析個数が増大し
靭性が低下するので注意すべきである。However, if the amount is too high, problems will appear in terms of physical properties and segregation will likely occur. That is, Cr contributes to improving the strength of the weld metal, but care should be taken because if it exceeds 3.5%, the number of segregated particles will increase and the toughness will decrease.
MOもCrと同様溶接金属の強度を高める作用があるが
、2%を越えると偏析個数が増大し靭性が低下すると共
に溶接割れが発生し易くなる。Niは靭性及び強度を高
める極めて有益な元素であるが、14%を越えると偏析
個数が増大すると共に溶接割れが発生し易くなる。尚上
記金属元素は金属単体として加えてもよく、或はそれら
の合金や鉄合金の形で添加してもよいが、鉄分を除く上
記金属元素の全被覆剤中の含有率は15%以下にするこ
とが望まれる。しかして15%を越えると、粒度構成を
調整しても偏析を十分に抑制できなくなるからである。
尚本発明でいう金属粉又は合金粉とは、脱酸剤として併
用され得るFe−Mn,Fe−S1等は除外したものと
して考えるべきである。ところで被覆剤成分としては周
知の通り適量のスラグ生成剤、アーク安定剤、ガス発生
剤、脱酸剤が必要であり、所望に応じて上記以外の合金
添加剤も配合されるが、本発明においてもこれらの剤が
適宜配合されるべきことは当然である。Like Cr, MO also has the effect of increasing the strength of the weld metal, but when it exceeds 2%, the number of segregated particles increases, the toughness decreases, and weld cracks are likely to occur. Ni is an extremely useful element that increases toughness and strength, but if it exceeds 14%, the number of segregated particles increases and weld cracking becomes more likely to occur. The above metal elements may be added as single metals, or in the form of their alloys or iron alloys, but the content of the above metal elements, excluding iron, in the total coating material must be 15% or less. It is desirable to do so. However, if it exceeds 15%, segregation cannot be sufficiently suppressed even if the particle size structure is adjusted.
Note that the metal powder or alloy powder in the present invention should be considered as excluding Fe-Mn, Fe-S1, etc., which can be used in combination as a deoxidizing agent. By the way, as is well known, suitable amounts of a slag forming agent, an arc stabilizer, a gas generating agent, and a deoxidizing agent are required as coating material components, and alloy additives other than those mentioned above may be added as desired. It goes without saying that these agents should be appropriately blended.
このうち上記必須成分を含めて代表的なものを例示すれ
ば下記の通りである。〔アーク安定剤〕
方解石、毒重石、ルチール、鋭錐石、イルミナイト、軟
マンガン鉱、鉄粉、珪酸カリ等。Among these, typical examples including the above-mentioned essential components are as follows. [Arc stabilizer] Calcite, toxite, rutile, anatase, illuminite, soft manganite, iron powder, potassium silicate, etc.
珪酸鉱物(珪砂、長石、タルク、マイカ等)、炭酸鉱物
(方解石等)、酸化物(ルチール、イルミナイト、鉄鉱
石、軟マンガン鉱等)、弗化物(螢石、氷晶石等)等。Silicate minerals (silica sand, feldspar, talc, mica, etc.), carbonate minerals (calcite, etc.), oxides (rutile, illuminite, iron ore, soft manganese, etc.), fluorides (fluorite, cryolite, etc.), etc.
炭酸鉱物、木屑、殿粉等。 Carbonate minerals, wood chips, starch, etc.
Fe−Mn,Fe−Si,Fe−Ti,Fe−Al,M
n,Si,Ti,At等。Fe-Mn, Fe-Si, Fe-Ti, Fe-Al, M
n, Si, Ti, At, etc.
Si,Mn,Cu,Cr,CO,Ni,W等。 Si, Mn, Cu, Cr, CO, Ni, W, etc.
このほか従来の低水素系被覆アーク溶接棒と同様被覆剤
中に鉄粉を配合し、溶接能率を高めることも有効である
。しかし40%を越えるとアークが不安定になり、特に
立向姿勢での溶接作業性が悪くなる。更に被覆剤や鋼心
線中に混入した微量のB,Nb,V,P或はそれらの酸
化物は、溶接金属の切欠靭性を箸しく阻害する。In addition, it is also effective to incorporate iron powder into the coating material to increase welding efficiency, similar to conventional low-hydrogen coated arc welding rods. However, if it exceeds 40%, the arc becomes unstable and welding workability, especially in a vertical position, deteriorates. Furthermore, trace amounts of B, Nb, V, P, or their oxides mixed into the coating material or the steel core material seriously impede the notch toughness of the weld metal.
そこでこれら不純元素の混入による障害を定量的に確認
すべく実験を行なつた結果、被覆剤中の(B+N・b+
V+P)の総含有率(酸化物の場合はB,Nb,,Pに
換算した値)を0.035q6以下に抑えると共に、鋼
心線中の同含有率を0.015%以下に抑えてやれば、
これらの不純元素含有による障害を殆んど無視し得る程
度に抑えることができる。ところで本発明で使用する被
覆剤は、前述の必須成分を必要により上記各剤と共に配
合し、珪酸ナトリウムや珪酸カリウム等の粘結剤と共に
混練して鋼心線の外周に塗布されるが、塗布時の生産性
や溶接棒の性能は、被覆剤原料中の金属粉を除く原料の
粒度構成にも相当影響されることが判明した。Therefore, as a result of conducting experiments to quantitatively confirm the damage caused by the contamination of these impurity elements, we found that (B+N・b+
Keep the total content (in the case of oxides, converted to B, Nb, P) of V + P) to 0.035q6 or less, and also keep the content in the steel core wire to 0.015% or less. Ba,
Problems caused by the inclusion of these impurity elements can be suppressed to an almost negligible level. By the way, the coating agent used in the present invention is mixed with the above-mentioned essential ingredients and the above-mentioned agents as necessary, and is kneaded with a binder such as sodium silicate or potassium silicate, and then applied to the outer periphery of the steel core wire. It has been found that the productivity and performance of welding rods are significantly affected by the particle size composition of the coating materials, excluding metal powder.
即ち種々実験の結果、金属粉を除く被覆剤原料のうち7
4μ以下の微粒子が25%を越えると、アークカが弱く
且つ溶融速度が低下して偏析個数が増大し、溶接作業性
が低下すると共に、溶接棒製造時に乾燥割れが著しくな
つて歩留りが低下する。また296μを越える粗粒物が
含まれていると、塗布工程で被覆剤のすベリが悪くなり
生産性が低下すると共に、溶接時にスパツタが多発する
。従つて金属粉を除く他の被覆剤原料の粒度構成は、2
96μ以下でなければならず、その上に74μ以下が2
5%以下、74〜296μが75%以上の条件を満たす
ものが最適である。ところで本発明では、特に被覆剤に
配合する金属粉及び合金粉の粗粒物含有率を一定値以下
に設定し、それら金属及び合金のマクロ偏析を減じたと
ころに最大の特徴があるが、第2図の結果からも明らか
な様に偏析個数を零にすることは困難である。そこで偏
析残留による溶接金属の性能低下を心線組成の改善によ
つて補うべく研究を行なつた。その結果心線中の炭素含
有量を極力少なくしてやれば、同一の偏析量であつても
溶接金属の物性を大幅に改善し得ることが判明した。即
ち溶接金属内におけるNi等の濃度の高い部分は、他の
部分に比べて変態点が低く、凝固過程では変態開始域か
ら未変態域に炭素が拡散する為、炭素は偏析部に集積さ
れる傾向がある。この炭素集積部の組織は極めて硬く、
衝撃力を受けたときに応力集中を起こして破断し易い。
ところが炭素含有量の少ない心線を使用すると炭素の集
積が少なくなり、局部的な硬度増加傾向が抑制される。
その結果マクロ偏析部に生じる応力集中が緩和され、偏
析数の減少とも相俟つて溶接金属の機械的性質殊に低温
靭性は大幅に改善される。これらの理由から心線中の炭
素含有量は少ないほど好まれるが、後記第3図の実験結
果からも明らかな様に、炭素含有率が0.01%以下の
鋼心線を使用すれば、偏析部の硬質化を十分に抑制でき
る。本発明は概略以上の様に構成されており、特に金属
粉及び合金粉、並びにその他の被覆剤原料の粒度構成を
適正に調整することによつて、偏析の少ない高品質の溶
接金属を与える低水素系被覆アーク溶接棒を提供し得る
ことになつた。That is, as a result of various experiments, 7 of the coating material raw materials excluding metal powder
If the content of fine particles of 4μ or less exceeds 25%, the arc force will be weak and the melting rate will decrease, the number of segregated particles will increase, welding workability will decrease, and dry cracking will become significant during welding rod production, resulting in a decrease in yield. Further, if coarse particles exceeding 296 μm are included, the coating material becomes difficult to coat during the coating process, reducing productivity and causing frequent spatter during welding. Therefore, the particle size structure of other coating material raw materials excluding metal powder is 2.
It must be 96μ or less, and 74μ or less is 2
Optimal is one that satisfies the conditions of 5% or less and 74-296μ of 75% or more. By the way, the greatest feature of the present invention is that the coarse particle content of the metal powder and alloy powder blended into the coating material is set below a certain value, thereby reducing the macro segregation of these metals and alloys. As is clear from the results in Figure 2, it is difficult to reduce the number of segregated particles to zero. Therefore, we conducted research to compensate for the decline in weld metal performance due to residual segregation by improving the core wire composition. As a result, it was found that by reducing the carbon content in the core wire as much as possible, the physical properties of the weld metal could be significantly improved even with the same amount of segregation. In other words, areas with a high concentration of Ni, etc. in the weld metal have a lower transformation point than other areas, and during the solidification process, carbon diffuses from the transformation start area to the untransformed area, so carbon is accumulated in the segregated area. Tend. The structure of this carbon accumulation area is extremely hard.
When subjected to impact force, stress concentration occurs and it is easy to break.
However, if a core wire with a low carbon content is used, carbon accumulation will be reduced, and the tendency for local hardness to increase will be suppressed.
As a result, the stress concentration occurring in the macro-segregation area is alleviated, and together with the reduction in the number of segregations, the mechanical properties, especially the low-temperature toughness, of the weld metal are significantly improved. For these reasons, the lower the carbon content in the core wire, the better; however, as is clear from the experimental results shown in Figure 3 below, if a steel core wire with a carbon content of 0.01% or less is used, Hardening of the segregated portion can be sufficiently suppressed. The present invention is constructed as described above, and in particular, by appropriately adjusting the particle size structure of metal powder, alloy powder, and other coating material raw materials, a high-quality weld metal with less segregation can be obtained. It is now possible to provide a hydrogen-based coated arc welding rod.
次に実験例を示す。Next, an experimental example will be shown.
実施例 1
第1表に示す成分組成の被覆剤を炭素量006%の炭素
鋼心線(5wr1nφ×400咽1)の外周に I塗布
して低水素系被覆アーク溶接棒を作製し、各溶接棒を用
いた場合の作業性及び溶接金属の偏析個数(第2図の場
合と同様にして測定)を調べた。Example 1 A low-hydrogen coated arc welding rod was prepared by coating the outer periphery of a carbon steel core wire (5wr 1nφ x 400mm) with a carbon content of 0.06% with a coating material having the composition shown in Table 1, and each welding The workability and the number of segregated weld metals (measured in the same manner as in FIG. 2) when using a rod were investigated.
浩果を第1表に一括して示す。但し第1表においで※1
〜※5は下記の意味を示している。※1:JISG23
O2のFSi3該当品で、粒度構成は、74μ以下が6
0%、
74〜105μが21%、105〜
149μが14%、149〜250μが
5%のものを用いた。Hiroka is shown in Table 1. However, in Table 1 *1
~*5 indicates the following meaning. *1: JISG23
For O2 FSi3 applicable products, the particle size composition is 74μ or less.
0%, 21% of 74-105μ, 14% of 105-149μ, and 5% of 149-250μ.
※2:JISG23llのMMnE該当品で、粒度構成
は、74μ以下が73%、74〜105μが11q6、
105〜149μが13C!11149〜250μが3
%のものを用いた。*2: JISG23ll MMnE applicable product, particle size composition is 73% below 74μ, 11q6 between 74μ and 105μ,
105~149μ is 13C! 11149~250μ is 3
% was used.
※3:JISG2l3のMcr該当品。*3: JISG2l3 Mcr applicable product.
※4:JISG23O7のFMOL該当品で表中の数字
はMO換算値。*4: For JIS G23O7 FMOL applicable products, the numbers in the table are MO conversion values.
※5:At2O3,K2O,Na2O,TiO2,Si
C2などを示す。*5: At2O3, K2O, Na2O, TiO2, Si
Indicates C2 etc.
第1表より次の様に考察することができる。From Table 1, it can be considered as follows.
(1)符号1〜3はNi粉等の粒度を調整していない従
来棒で、偏析個数が相当多い。(2)これに対し符号4
〜8はNi粉等を149μ以上の粗粒物が20%以下に
なる様に粒度調整した実施例で、Ni粉等が2%である
符号1と4の比較、同8%である符号2と5,6の比較
、同14%である符号3と7,8の比較を夫々行なつて
みると、偏析個数が大幅に低減できていることが分る。(1) Codes 1 to 3 are conventional bars in which the particle size of Ni powder or the like is not adjusted, and the number of segregated pieces is quite large. (2) On the other hand, code 4
~8 is an example in which the particle size of Ni powder, etc. was adjusted so that the coarse particles of 149μ or more were 20% or less, and a comparison of codes 1 and 4, where the Ni powder, etc. was 2%, and code 2, where the Ni powder, etc. was 8%. When comparing numbers 3 and 7 and 8, which are 14%, respectively, it can be seen that the number of segregated particles can be significantly reduced.
(3)符号9及び10はNi粉が0.50!Iと少ない
為、粒度構成に関係なく偏析個数は少なく、また符号1
1及び12はNi粉が16%と多すぎる為、粒度を適正
に調整しても偏析個数はあまり減少しない。(3) Codes 9 and 10 are Ni powder at 0.50! I, the number of segregated particles is small regardless of the particle size structure, and the number of segregated particles is 1.
In Nos. 1 and 12, the amount of Ni powder is too high at 16%, so even if the particle size is adjusted appropriately, the number of segregated particles does not decrease much.
(4)符号13は、CaF2量が不足する為溶融スラグ
の流動性が悪くピツト欠陥が現われ、また符号14では
CaF2量が多すぎる為アークが不安定であり、何れも
溶接作業性が悪い。(4) In case of code 13, the fluidity of the molten slag is poor due to insufficient amount of CaF2 and pit defects appear, and in case of code 14, the arc is unstable due to too large amount of CaF2, and welding workability is poor in both cases.
(5)符号15は、炭酸塩が多すぎる為溶込みが深くな
りすぎるきらいがあり、また符号16は炭塩が不足する
為シールド効果が不十分になる。(5) Since the number 15 has too much carbonate, the penetration tends to be too deep, and the number 16 has insufficient carbonate, so the shielding effect is insufficient.
(6)符号17は、金属粉及び合金粉以外の被覆剤原料
に占める74μ以下の微粒物の割合が多すぎる為、アー
クカが弱くなつて溶融速度が遅くなり、偏析個数が増加
する。また符号18は他の被覆剤原料中の296μ以上
の粗粒物の割合が多すぎる為製造時の塗装性が悪く、且
つ溶接時にスパツタが多発する。(7)符号19〜23
は、Crの含有率及び粒度構成を変化させたもので、C
r含有率が高くなる程、またCr粉中の149μ以上の
粗粒物量が多くなる程、偏析個数は増加する。(6) No. 17 indicates that the proportion of fine particles of 74 μm or less in the coating material raw materials other than metal powders and alloy powders is too large, so the arc becomes weak, the melting rate becomes slow, and the number of segregated particles increases. Further, in the case of No. 18, since the proportion of coarse particles of 296 μm or more in other coating material raw materials is too high, the coating properties during manufacture are poor, and spatters occur frequently during welding. (7) Codes 19-23
is one in which the Cr content and particle size structure are changed, and C
The higher the r content and the larger the amount of coarse particles of 149μ or more in the Cr powder, the more the number of segregated particles increases.
(8)符号24〜28は、MOの含有率及び粒度構成を
変化させたもので、MO含有率が高くなる程、またMO
粉中の149μ以上の粗粒物量が多くなる程、偏析個数
が増加する。(8) Codes 24 to 28 are obtained by changing the MO content and particle size structure, and the higher the MO content, the more MO
As the amount of coarse particles of 149μ or more in the powder increases, the number of segregated particles increases.
尚第3図は符号5及び7の被覆剤を使用した場合につい
て、鋼心線中の炭素量と偏析部の硬さの関係を示したグ
ラフであり、炭素含有率が0.01%以下である心線を
使用すれば、マクロ偏析が多少起こつても、偏析部の硬
質化が抑制される為耐割れ性が改善される。Fig. 3 is a graph showing the relationship between the amount of carbon in the steel core wire and the hardness of the segregated part when coating materials 5 and 7 are used. If a certain core wire is used, even if some macro-segregation occurs, the hardening of the segregated portion is suppressed and crack resistance is improved.
実験例 2
第2表に示す如く成分組成及び粒度構成がすべて本発明
の要件を満足する被覆剤を、炭素量0.0.7%の鋼心
線(4.0rmφ×400wr!nl)の外周に塗布し
て低水素系被覆アーク溶接棒を製造した。Experimental Example 2 A coating material whose composition and particle size structure all satisfy the requirements of the present invention as shown in Table 2 was applied to the outer periphery of a steel core wire (4.0rmφ×400wr!nl) with a carbon content of 0.0.7%. A low hydrogen-based coated arc welding rod was manufactured by applying the same to
この溶接棒を使用して溶接作業性及びJISZ32l2
により溶接金属の引張り強さ及び衝撃強さ(−20℃に
おけるシヤルピ一衝撃値)を調べ鳩結果を第2表に示す
。第2表からも明らかな様に、本発明の溶接棒を使用す
ると、良好な溶接作業性が得られると共に、金属粉や合
金粉の偏析が起こらず、低温靭性及び引張り強さの優れ
た溶接金属を得ることができる。Using this welding rod, welding workability and JIS Z32l2
The tensile strength and impact strength (Sharpy impact value at -20°C) of the weld metal were investigated using Table 2. As is clear from Table 2, when the welding rod of the present invention is used, not only good welding workability can be obtained, but also segregation of metal powder and alloy powder does not occur, and welding with excellent low-temperature toughness and tensile strength can be achieved. You can get metal.
実験例 3第3表に示す成分組成の被覆剤を鋼心線(4
.0糎φX4OOrWfLt)の外周に塗布し、低水素
系被覆アーク溶接棒を製造した。Experimental Example 3 A steel core wire (4
.. 0 starch (φ
尚本例では、特に被覆剤及び心線中の(B+Nb+V+
P)の含有率の影響を調べる為、これらについても併記
した。尚被覆剤原料の粒度構成は、すべて本発明の要件
を満たす様に調整した。得られた各溶接棒を用いて第2
表の場合と同様の条件で溶接を行ない、溶接作業性及び
溶接金属の物性を調べた。In this example, (B+Nb+V+
In order to investigate the influence of the content rate of P), these are also listed. The particle size structure of the coating material raw material was adjusted to meet the requirements of the present invention. Using each obtained welding rod, the second
Welding was carried out under the same conditions as in the table, and the welding workability and physical properties of the weld metal were investigated.
結果を第3表に一括して示す。第3表より次の様に考察
できる。(1)符号36〜40は、炭酸塩、CaF2又
は鉄粉の配合率が規定範囲を外れる比較例で、何れも溶
接作業性が悪い。The results are summarized in Table 3. From Table 3, the following can be considered. (1) Reference numbers 36 to 40 are comparative examples in which the blending ratio of carbonate, CaF2, or iron powder is out of the specified range, and welding workability is poor in all of them.
(2)符号34は従来の60キロ級の溶接棒で、(B+
Nb++P)量が好適範囲を外れている為、同含有量が
好適範囲内である符号35に比べて衝撃強さが低い。(2) The code 34 is a conventional 60 kg class welding rod (B+
Since the amount of Nb++P) is outside the preferred range, the impact strength is lower than that of No. 35, in which the same content is within the preferred range.
(3)符号41は従来の80キロ級の溶接棒で、(B+
Nb+V+P)量が好適範囲を外れている為、同含有量
が好適範囲内である符号42に比べて衝撃強さが低い。(3) The code 41 is a conventional 80 kg class welding rod (B+
Since the amount of Nb+V+P) is outside the preferred range, the impact strength is lower than that of code 42 in which the same content is within the preferred range.
(4)符号43は適量の鉄粉を含む80キロ級の溶接棒
で、高い引張り強さと衝撃強さが得られる。(4) Reference numeral 43 is an 80kg welding rod containing an appropriate amount of iron powder, which provides high tensile strength and impact strength.
(5)符号44は本発明の要件を満足する被覆剤中に多
量のNiを配合した80キロ級の溶接棒で良好な強度、
靭性を有している。(6)符号45,46は本発明の要
件を満足する60キロ級及び100キロ級の溶接棒で、
溶接作業性及び溶接金属の物性共に優れている。(5) Reference numeral 44 is an 80kg welding rod with a coating material containing a large amount of Ni, which satisfies the requirements of the present invention, and has good strength and
It has toughness. (6) Symbols 45 and 46 are 60 kg class and 100 kg class welding rods that satisfy the requirements of the present invention,
Excellent welding workability and physical properties of weld metal.
尚第4,5図は60キロ級及び80キロ級の溶接棒を対
象として従来棒(符号34,41)又は本発明棒(符号
35,42)を用いて得た溶接金属の熱処理前後のもの
について衝撃遷移曲線を示したものである。Figures 4 and 5 show weld metals before and after heat treatment obtained using conventional rods (numbers 34, 41) or the present invention rods (numbers 35, 42) for 60 kg and 80 kg class welding rods. The shock transition curve is shown for .
この図からも明らかな様に、本発明の溶接棒を使用する
ことにより、従来棒を使用した場合に比べて耐衝撃性能
の優れた溶接金属を得ることができる。As is clear from this figure, by using the welding rod of the present invention, it is possible to obtain a weld metal with superior impact resistance compared to the case where a conventional rod is used.
第1図は溶接金属のマクロ偏析を起こした部分のEPM
Aチヤート、第2図はNi,Cr及びMO粉の粒度構成
と偏析個数の関係を示すグラフ、第3図は心線中の炭素
量と偏析部の硬さの関係を示すグラフ、第4,5図は実
験例で得た溶接金属の衝撃遷移曲線を夫々示す。Figure 1 shows the EPM of the part where macro segregation of weld metal occurred.
Chart A, Figure 2 is a graph showing the relationship between the particle size structure of Ni, Cr and MO powder and the number of segregated particles, Figure 3 is a graph showing the relationship between the amount of carbon in the core wire and the hardness of the segregated part, 4th, Figure 5 shows the impact transition curves of the weld metals obtained in the experimental examples.
Claims (1)
なる群から選択される1種以上の炭酸塩を合計で25〜
55重量%、CaF_2を2〜30重量%、金属粉及び
/又は合金粉を15重量%以下並びに固着剤を主成分と
して含有する被覆剤を鋼心線外周に塗布してなる低水素
系被覆アーク溶接棒において、金属粉及び/又は合金粉
を除く上記被覆剤原料の粒度を、296μ以下で且つ7
4μ以下のものの比率が25重量%以下となる様に調整
すると共に、金属粉及び/又は合金粉の粒度について、
149μ以上のものの比率20重量%以下となる様に調
整したことを特徴とする低水素系被覆アーク溶接棒。 2 特許請求の範囲第1項において、金属粉及び/又は
合金粉が、14重量%以下のNi、3.5重量%以下の
Cr、並びにMo換算で2重量%以下のMo及び/又は
Fe−Moよりなる群から選択される1種以上である低
水素系被覆アーク溶接棒。 3 特許請求の範囲第1又は第2項において、C含有率
が0.01重量%以下である鋼心線を用いた低水素系被
覆アーク溶接棒。[Claims] 1. A total of 25 to 10 carbonates selected from the group consisting of CaCO_3, MgCO_3 and BaCO_3.
A low hydrogen-based coated arc made by applying a coating material containing 55% by weight, 2 to 30% by weight of CaF_2, 15% by weight or less of metal powder and/or alloy powder, and a fixing agent to the outer periphery of the steel core wire. In the welding rod, the particle size of the coating material raw material excluding metal powder and/or alloy powder is 296 μ or less and 7
In addition to adjusting the ratio of particles of 4μ or less to 25% by weight or less, the particle size of the metal powder and/or alloy powder is adjusted.
A low-hydrogen-based coated arc welding rod, characterized in that the ratio of electrodes of 149μ or more is adjusted to be 20% by weight or less. 2. In claim 1, the metal powder and/or alloy powder contains 14% by weight or less of Ni, 3.5% by weight or less of Cr, and 2% by weight or less of Mo and/or Fe- A low hydrogen-based coated arc welding rod that is one or more types selected from the group consisting of Mo. 3. A low hydrogen-based coated arc welding rod using a steel core wire having a C content of 0.01% by weight or less, as set forth in claim 1 or 2.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15741580A JPS5922633B2 (en) | 1980-11-07 | 1980-11-07 | Low hydrogen coated arc welding rod |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP15741580A JPS5922633B2 (en) | 1980-11-07 | 1980-11-07 | Low hydrogen coated arc welding rod |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5781997A JPS5781997A (en) | 1982-05-22 |
| JPS5922633B2 true JPS5922633B2 (en) | 1984-05-28 |
Family
ID=15649131
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP15741580A Expired JPS5922633B2 (en) | 1980-11-07 | 1980-11-07 | Low hydrogen coated arc welding rod |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5922633B2 (en) |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6186132U (en) * | 1984-11-13 | 1986-06-06 | ||
| JPH026100U (en) * | 1988-06-27 | 1990-01-16 | ||
| WO2018168480A1 (en) | 2017-03-13 | 2018-09-20 | 三菱重工業株式会社 | Eddy current flaw detecting probe |
Families Citing this family (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58209499A (en) * | 1982-05-31 | 1983-12-06 | Kobe Steel Ltd | Low hydrogen covered arc welding rod |
| GB2259113B (en) * | 1991-02-28 | 1995-05-17 | Ishigaki Mech Ind | Pump having a single or a plurality of helical blades |
| JP2711069B2 (en) * | 1994-03-14 | 1998-02-10 | 株式会社神戸製鋼所 | Low hydrogen coated arc welding rod |
| JP2942142B2 (en) * | 1994-03-31 | 1999-08-30 | 株式会社神戸製鋼所 | Low hydrogen coated arc welding rod |
| JP2878593B2 (en) * | 1994-03-31 | 1999-04-05 | 株式会社神戸製鋼所 | Low hydrogen coated arc welding rod |
| JP4933487B2 (en) * | 2008-05-21 | 2012-05-16 | 旭洋造船株式会社 | Fuel efficient transport ship |
-
1980
- 1980-11-07 JP JP15741580A patent/JPS5922633B2/en not_active Expired
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6186132U (en) * | 1984-11-13 | 1986-06-06 | ||
| JPH026100U (en) * | 1988-06-27 | 1990-01-16 | ||
| WO2018168480A1 (en) | 2017-03-13 | 2018-09-20 | 三菱重工業株式会社 | Eddy current flaw detecting probe |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5781997A (en) | 1982-05-22 |
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