JP7638595B2 - Low hydrogen iron powder covered electrode - Google Patents
Low hydrogen iron powder covered electrode Download PDFInfo
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- JP7638595B2 JP7638595B2 JP2021056217A JP2021056217A JP7638595B2 JP 7638595 B2 JP7638595 B2 JP 7638595B2 JP 2021056217 A JP2021056217 A JP 2021056217A JP 2021056217 A JP2021056217 A JP 2021056217A JP 7638595 B2 JP7638595 B2 JP 7638595B2
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- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 title claims description 30
- 239000001257 hydrogen Substances 0.000 title claims description 23
- 229910052739 hydrogen Inorganic materials 0.000 title claims description 23
- 125000004435 hydrogen atom Chemical class [H]* 0.000 title 1
- 238000003466 welding Methods 0.000 claims description 104
- 229910052751 metal Inorganic materials 0.000 claims description 101
- 239000002184 metal Substances 0.000 claims description 101
- 239000011248 coating agent Substances 0.000 claims description 50
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 37
- 238000000576 coating method Methods 0.000 claims description 30
- 239000000463 material Substances 0.000 claims description 27
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 claims description 25
- 229910000831 Steel Inorganic materials 0.000 claims description 24
- 239000010959 steel Substances 0.000 claims description 24
- MCMNRKCIXSYSNV-UHFFFAOYSA-N Zirconium dioxide Chemical compound O=[Zr]=O MCMNRKCIXSYSNV-UHFFFAOYSA-N 0.000 claims description 18
- 229910001512 metal fluoride Inorganic materials 0.000 claims description 14
- 239000000377 silicon dioxide Substances 0.000 claims description 13
- KRHYYFGTRYWZRS-UHFFFAOYSA-M Fluoride anion Chemical compound [F-] KRHYYFGTRYWZRS-UHFFFAOYSA-M 0.000 claims description 12
- 229910052681 coesite Inorganic materials 0.000 claims description 12
- 229910052906 cristobalite Inorganic materials 0.000 claims description 12
- 235000012245 magnesium oxide Nutrition 0.000 claims description 12
- 229910052700 potassium Inorganic materials 0.000 claims description 12
- 235000012239 silicon dioxide Nutrition 0.000 claims description 12
- 229910052682 stishovite Inorganic materials 0.000 claims description 12
- 229910052905 tridymite Inorganic materials 0.000 claims description 12
- 150000004649 carbonic acid derivatives Chemical class 0.000 claims description 10
- 229910052708 sodium Inorganic materials 0.000 claims description 10
- 229910052748 manganese Inorganic materials 0.000 claims description 9
- 229910052804 chromium Inorganic materials 0.000 claims description 8
- 239000000203 mixture Substances 0.000 claims description 8
- 229910052750 molybdenum Inorganic materials 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 229910052593 corundum Inorganic materials 0.000 claims description 6
- 229910001845 yogo sapphire Inorganic materials 0.000 claims description 6
- 239000012535 impurity Substances 0.000 claims description 5
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical class [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims description 3
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 239000011324 bead Substances 0.000 description 34
- 239000002893 slag Substances 0.000 description 33
- 239000010936 titanium Substances 0.000 description 25
- 239000011734 sodium Substances 0.000 description 24
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 18
- 230000000694 effects Effects 0.000 description 17
- 238000005452 bending Methods 0.000 description 13
- 238000002844 melting Methods 0.000 description 13
- 230000008018 melting Effects 0.000 description 13
- 229910052710 silicon Inorganic materials 0.000 description 12
- 239000000395 magnesium oxide Substances 0.000 description 10
- 239000011575 calcium Substances 0.000 description 9
- 230000007423 decrease Effects 0.000 description 9
- 229910052719 titanium Inorganic materials 0.000 description 8
- 230000007547 defect Effects 0.000 description 7
- 238000005516 engineering process Methods 0.000 description 7
- 229910052814 silicon oxide Inorganic materials 0.000 description 7
- 239000000523 sample Substances 0.000 description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 5
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 5
- 239000011777 magnesium Substances 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 235000019353 potassium silicate Nutrition 0.000 description 5
- 239000000843 powder Substances 0.000 description 5
- 239000010703 silicon Substances 0.000 description 5
- NTHWMYGWWRZVTN-UHFFFAOYSA-N sodium silicate Chemical compound [Na+].[Na+].[O-][Si]([O-])=O NTHWMYGWWRZVTN-UHFFFAOYSA-N 0.000 description 5
- 239000003795 chemical substances by application Substances 0.000 description 4
- 238000005538 encapsulation Methods 0.000 description 4
- 150000002222 fluorine compounds Chemical class 0.000 description 4
- 238000004519 manufacturing process Methods 0.000 description 4
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 4
- PUZPDOWCWNUUKD-UHFFFAOYSA-M sodium fluoride Chemical compound [F-].[Na+] PUZPDOWCWNUUKD-UHFFFAOYSA-M 0.000 description 4
- 230000000087 stabilizing effect Effects 0.000 description 4
- 238000002441 X-ray diffraction Methods 0.000 description 3
- DLHONNLASJQAHX-UHFFFAOYSA-N aluminum;potassium;oxygen(2-);silicon(4+) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[O-2].[Al+3].[Si+4].[Si+4].[Si+4].[K+] DLHONNLASJQAHX-UHFFFAOYSA-N 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000004576 sand Substances 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 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
- 229910017116 Fe—Mo Inorganic materials 0.000 description 2
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- 239000004111 Potassium silicate Substances 0.000 description 2
- 229910006639 Si—Mn Inorganic materials 0.000 description 2
- 239000004115 Sodium Silicate Substances 0.000 description 2
- 229910045601 alloy Inorganic materials 0.000 description 2
- 239000000956 alloy Substances 0.000 description 2
- BYFGZMCJNACEKR-UHFFFAOYSA-N aluminium(i) oxide Chemical compound [Al]O[Al] BYFGZMCJNACEKR-UHFFFAOYSA-N 0.000 description 2
- 238000001636 atomic emission spectroscopy Methods 0.000 description 2
- AOWKSNWVBZGMTJ-UHFFFAOYSA-N calcium titanate Chemical compound [Ca+2].[O-][Ti]([O-])=O AOWKSNWVBZGMTJ-UHFFFAOYSA-N 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 239000010949 copper Substances 0.000 description 2
- 230000002950 deficient Effects 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000004927 fusion Effects 0.000 description 2
- 239000011521 glass Substances 0.000 description 2
- 238000009863 impact test Methods 0.000 description 2
- PQXKHYXIUOZZFA-UHFFFAOYSA-M lithium fluoride Chemical compound [Li+].[F-] PQXKHYXIUOZZFA-UHFFFAOYSA-M 0.000 description 2
- 239000003973 paint Substances 0.000 description 2
- 239000011591 potassium Substances 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
- 230000001681 protective effect Effects 0.000 description 2
- 238000004445 quantitative analysis Methods 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- -1 sodium fluoride Chemical class 0.000 description 2
- 239000011775 sodium fluoride Substances 0.000 description 2
- 235000013024 sodium fluoride Nutrition 0.000 description 2
- 229910052911 sodium silicate Inorganic materials 0.000 description 2
- 238000009864 tensile test Methods 0.000 description 2
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 2
- 239000010456 wollastonite Substances 0.000 description 2
- 229910052882 wollastonite Inorganic materials 0.000 description 2
- 229910052845 zircon Inorganic materials 0.000 description 2
- GFQYVLUOOAAOGM-UHFFFAOYSA-N zirconium(iv) silicate Chemical compound [Zr+4].[O-][Si]([O-])([O-])[O-] GFQYVLUOOAAOGM-UHFFFAOYSA-N 0.000 description 2
- IRPGOXJVTQTAAN-UHFFFAOYSA-N 2,2,3,3,3-pentafluoropropanal Chemical compound FC(F)(F)C(F)(F)C=O IRPGOXJVTQTAAN-UHFFFAOYSA-N 0.000 description 1
- 229910018072 Al 2 O 3 Inorganic materials 0.000 description 1
- KLZUFWVZNOTSEM-UHFFFAOYSA-K Aluminum fluoride Inorganic materials F[Al](F)F KLZUFWVZNOTSEM-UHFFFAOYSA-K 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910017060 Fe Cr Inorganic materials 0.000 description 1
- 229910000640 Fe alloy Inorganic materials 0.000 description 1
- 229910002544 Fe-Cr Inorganic materials 0.000 description 1
- 229910017082 Fe-Si Inorganic materials 0.000 description 1
- 229910002593 Fe-Ti Inorganic materials 0.000 description 1
- 229910017133 Fe—Si Inorganic materials 0.000 description 1
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 239000003513 alkali Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- AYJRCSIUFZENHW-DEQYMQKBSA-L barium(2+);oxomethanediolate Chemical compound [Ba+2].[O-][14C]([O-])=O AYJRCSIUFZENHW-DEQYMQKBSA-L 0.000 description 1
- 230000005540 biological transmission Effects 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 238000011088 calibration curve Methods 0.000 description 1
- UPHIPHFJVNKLMR-UHFFFAOYSA-N chromium iron Chemical compound [Cr].[Fe] UPHIPHFJVNKLMR-UHFFFAOYSA-N 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 230000008094 contradictory effect Effects 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 238000004993 emission spectroscopy Methods 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 239000010419 fine particle Substances 0.000 description 1
- 239000005357 flat glass Substances 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- KWLMIXQRALPRBC-UHFFFAOYSA-L hectorite Chemical compound [Li+].[OH-].[OH-].[Na+].[Mg+2].O1[Si]2([O-])O[Si]1([O-])O[Si]([O-])(O1)O[Si]1([O-])O2 KWLMIXQRALPRBC-UHFFFAOYSA-L 0.000 description 1
- 229910000271 hectorite Inorganic materials 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- ORUIBWPALBXDOA-UHFFFAOYSA-L magnesium fluoride Chemical compound [F-].[F-].[Mg+2] ORUIBWPALBXDOA-UHFFFAOYSA-L 0.000 description 1
- 229910001635 magnesium fluoride Inorganic materials 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
- 229910052618 mica group Inorganic materials 0.000 description 1
- 239000004570 mortar (masonry) Substances 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 238000007500 overflow downdraw method Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 229910052720 vanadium Inorganic materials 0.000 description 1
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- Nonmetallic Welding Materials (AREA)
Description
本発明は、特に直流電源を使用したアーク溶接において、アーク安定性が良好であり、引張強度が780MPa以上の強度が得られ、かつ良好な低温靭性と溶接継手の曲げ性能が得られる鉄粉低水素系被覆アーク溶接棒に関する。 The present invention relates to an iron powder low-hydrogen covered metal arc welding rod that has good arc stability, a tensile strength of 780 MPa or more, and good low-temperature toughness and bending performance of the welded joint, particularly in arc welding using a DC power source.
低水素系被覆アーク溶接棒は、アーク安定性が良好で、耐割れ性や溶接金属の低温靱性が優れていることから、拘束が強い箇所や高張力鋼の溶接に広く使用されている。 Low-hydrogen covered electrodes have good arc stability, excellent crack resistance, and low-temperature toughness of the weld metal, so they are widely used in areas with strong restraints and for welding high-tensile steel.
一方、最近の溶接構造物の大型化にともない、使用される鋼材の高強度化が要望されている。また、天然資源の開発を目的とした大型海洋構造物や球形タンク等では、安全性の確保のため、溶接金属の低温靱性の更なる向上や、強度を十分に確保するなど優れた機械的性能確保が重要となる。しかし、一般的に溶接金属の高強度化と低温靱性の両立は相反する特性のため、高強度化と低温靱性を両立する新たな手法の開発が望まれている。 On the other hand, with the recent increase in size of welded structures, there is a demand for higher strength steel materials to be used. Also, in order to ensure safety in large marine structures and spherical tanks aimed at the development of natural resources, it is important to further improve the low-temperature toughness of the weld metal and ensure excellent mechanical performance, such as by ensuring sufficient strength. However, since achieving both high strength and low-temperature toughness in weld metal are generally contradictory properties, there is a need to develop new methods that achieve both high strength and low-temperature toughness.
このような状況に対し、溶接金属の機械的性能の向上手段として、いくつかの提案がされている。例えば、特許文献1には、Ni含有量が1質量%以下でも低温靱性が優れた溶接金属を得ることを目的とした被覆アーク溶接棒に関する技術が開示されている。しかし、特許文献1に記載の技術では、直流電源を用いて溶接を行うと磁気吹きや被覆の片溶けが発生し易く十分な溶接作業性が確保できない問題点がある。 In response to this situation, several proposals have been made to improve the mechanical performance of weld metal. For example, Patent Document 1 discloses technology related to a covered metal arc welding rod that aims to obtain a weld metal with excellent low-temperature toughness even when the Ni content is 1 mass% or less. However, the technology described in Patent Document 1 has the problem that when welding is performed using a DC power source, magnetic blow and one-sided melting of the coating are likely to occur, making it difficult to ensure sufficient welding workability.
特許文献2には、490MPa級以上の鋼管円周を、直流電源を用いて多層盛溶接を行うと、アークの安定性に優れ、溶接金属の強度及び低温靱性が優れる低水素系被覆アーク溶接棒の技術が開示されている。しかし、この特許文献2の開示技術は、490MPa級以上の鋼管円周の多層盛溶接に適用されており、引張強さ550~650MPaの溶接材料についての技術である。このため、780MPa以上の溶接材料では十分な特性がえられない。 Patent Document 2 discloses a low-hydrogen covered electrode technology that, when multi-layer welding is performed on the circumference of a steel pipe of 490 MPa class or more using a DC power source, provides excellent arc stability and excellent weld metal strength and low-temperature toughness. However, the technology disclosed in Patent Document 2 is applied to multi-layer welding of the circumference of a steel pipe of 490 MPa class or more, and is a technology for welding materials with a tensile strength of 550 to 650 MPa. For this reason, sufficient characteristics cannot be obtained with welding materials of 780 MPa or more.
また、特許文献3には、溶着金属の引張強さが590MPa以上において安定した溶接金属の機械的性能、全姿勢溶接における良好な溶接作業性と低温靭性を確保する低水素系被覆アーク溶接棒の技術の開示がある。しかし、この特許文献3の開示技術では、Niを鋼心線に添加するため、溶接棒の価格が高くなる問題点があった。 Patent Document 3 also discloses technology for low-hydrogen covered metal arc welding rods that ensure stable mechanical performance of the weld metal when the tensile strength of the deposited metal is 590 MPa or more, good welding workability in all positions, and low-temperature toughness. However, the technology disclosed in Patent Document 3 has the problem that the welding rod is expensive because Ni is added to the steel core wire.
低水素系被覆アーク溶接棒は、一般的に国内では交流電源を用いて溶接するように設計されているが、最近では球形タンクや海洋構造物の海外における現場溶接など、より安価な電源装置となる直流電源で使用できる低水素系被覆アーク溶接棒の開発が望まれている。 Low-hydrogen covered electrodes are generally designed for use in Japan with AC power sources for welding, but recently there has been a demand for the development of low-hydrogen covered electrodes that can be used with DC power sources, which are cheaper power sources, for on-site welding of spherical tanks and marine structures overseas.
低水素系被覆アーク溶接棒を、直流電源を用いて溶接すると、磁気吹きや被覆剤の片溶けが生じてアークが不安定となり、健全なビードが得られないという課題がある。このため、直流電源を使用した場合においても、アークの安定性に優れ、溶接金属の機械性能が良好な鉄粉低水素系被覆アーク溶接棒の開発が望まれている。 When low-hydrogen covered metal arc welding rods are welded using a DC power source, magnetic blow and one-sided melting of the coating material can occur, making the arc unstable and preventing the production of a sound bead. For this reason, there is a need for the development of an iron powder low-hydrogen covered metal arc welding rod that has excellent arc stability and good mechanical properties of the weld metal, even when using a DC power source.
本発明は、かかる問題点に鑑みて案出されたものであって、より高強度の780MPa級高張力鋼での直流電源を用いた多層盛溶接において、アーク安定性等の溶接作業性が良好、溶接継手が優れた低温靭性と曲げ加工性を発現する780MPa級高張力鋼用の鉄粉低水素系被覆アーク溶接棒を提供することを目的とする。 The present invention was devised in consideration of these problems, and aims to provide an iron powder, low hydrogen type covered metal arc welding rod for 780 MPa class high tensile steel, which has good welding workability such as arc stability, and which produces welded joints with excellent low temperature toughness and bending workability when used in multi-layer welding using a DC power source with higher strength 780 MPa class high tensile steel.
本発明は、鋼心線に被覆剤が塗装されている、780MPa級高張力鋼での直流電源を用いた多層盛溶接用の鉄粉低水素系被覆アーク溶接棒において、被覆剤の被覆率が溶接棒全質量に対する質量%で30~45%であり、前記被覆剤の組成が被覆剤全質量に対する質量%で、Mn:3.0~6.0%、Ni:3.5~7.5%、Mo:0.3~1.3%、Cr:0.2~1.0%、Si:2.0~5.0%、Si酸化物のSiO2換算値の合計:3.5~7.5%、Ti:0.2~1.5%、Ti酸化物のTiO2換算値の合計:1.0~5.0%、一種或いは二種以上の金属炭酸塩の合計:25~45%、一種或いは二種以上の金属弗化物の合計:5~15%を含有し、Al酸化物のAl2O3換算値の合計:2.0%以下、Mg酸化物のMgO換算値の合計:0.8%以下であり、Na酸化物、Na弗化物、K酸化物及びK弗化物の1種または2種以上の合計:Na換算値とK換算値の合計で1.5~3.0%を含有し、かつ、前記Mn、Ni、Mo及びCrが式(1)で150~300であり、さらにFe:20~30%を含有し、不純物からなる残部の合計が1.0%以下である被覆剤を塗装してあることを特徴とする。 The present invention relates to an iron powder low hydrogen type covered electrode for multi-pass welding of 780 MPa class high tensile steel using a DC power source , in which a steel core wire is coated with a covering agent, the covering rate of the covering agent being 30 to 45% in mass % relative to the total mass of the welding electrode, the composition of the covering agent being, in mass % relative to the total mass of the covering agent, 3.0 to 6.0% Mn, 3.5 to 7.5% Ni, 0.3 to 1.3% Mo, 0.2 to 1.0% Cr, 2.0 to 5.0% Si, a total of SiO2 converted values of Si oxides : 3.5 to 7.5%, 0.2 to 1.5% Ti, a total of Ti oxides in TiO2 converted values: 1.0 to 5.0%, a total of one or more metal carbonates: 25 to 45%, a total of one or more metal fluorides: 5 to 15%, and the Al oxide Al2O the total of Mn, Ni, Mo and Cr in terms of formula ( 1 ) is 150-300, Fe is 20-30%, and the total of the remainder consisting of impurities is 1.0% or less.
2.3×[Mn]+38.5×[Ni]+4.2×[Mo]+2.1×[Cr]・・・式(1)
但し、[ ]は、各成分の被覆剤全質量に対する質量%を示す。
2.3 × [Mn] + 38.5 × [Ni] + 4.2 × [Mo] + 2.1 × [Cr] ... formula (1)
Here, the brackets [ ] indicate the mass % of each component relative to the total mass of the coating agent.
また、前記被覆剤が被覆剤全質量に対する質量%で、Ca酸化物のCaO換算値の合計:0.5%以下であることを特徴とする鉄粉低水素系被覆アーク溶接棒にある。 The coating material is also characterized in that the total CaO equivalent value of Ca oxides is 0.5% or less, expressed as a percentage by mass relative to the total mass of the coating material.
さらに、前記被覆剤が被覆剤全質量に対する質量%で、Zr酸化物のZrO2換算値の合計:1.5%以下であることを特徴とする鉄粉低水素系被覆アーク溶接棒にある。 The present invention further provides an iron powder low hydrogen type covered metal arc welding electrode, characterized in that the coating material has a total content of Zr oxide calculated as ZrO2 of 1.5% or less, expressed as mass% based on the total mass of the coating material.
本発明を適用した鉄粉低水素系被覆アーク溶接棒によれば、780MPa級高張力鋼での直流電源を用いた多層盛溶接において、鋼材と同等以上の強度が得られ、アーク安定性等の溶接作業性が良好であり、かつ、低温での安定した靱性が得られ、作製した溶接継手において良好な曲げ性能が得られる。したがって、各種鋼構造物に対する溶接継手の信頼性を大幅に向上することができる。 The low-hydrogen iron powder covered metal arc welding electrode of the present invention achieves strength equal to or greater than that of steel in multi-layer welding of 780 MPa-class high-tensile steel using a DC power source, provides good welding workability such as arc stability, and provides stable toughness at low temperatures, resulting in good bending performance in the welded joints produced. Therefore, the reliability of welded joints for various steel structures can be significantly improved.
本発明者らは、上述した課題を解決するために、780MPa級高張力鋼での直流電源を用いた多層盛溶接において、この強度と同等以上の強度アーク安定性等の良好な溶接作業性、安定した低温靱性、かつ、作製した溶接継手の良好な曲げ性能を溶接後の溶接継ぎ手において得ることが可能な鉄粉低水素系被覆アーク溶接棒、特にその被覆剤の成分組成について詳細に検討した。 In order to solve the above-mentioned problems, the inventors conducted detailed research into an iron powder low-hydrogen covered metal arc welding electrode, and in particular the component composition of its coating, that can provide a strength equal to or greater than this strength, good welding workability such as arc stability, stable low-temperature toughness, and good bending performance of the welded joint after welding when using a DC power source for multi-layer welding of 780 MPa-class high-tensile steel.
その結果、以下の知見が得られ、その方針に従い各種成分の調整を行うことで本発明を見出した。 As a result, the following findings were obtained, and the present invention was developed by adjusting the various ingredients according to these findings.
(1)Mn、Ni、Mo及びCrの含有量を適量とすることで溶接金属の強度及び溶接継手の良好な曲げ性能を確保することができること。 (1) By adjusting the content of Mn, Ni, Mo, and Cr to an appropriate amount, it is possible to ensure the strength of the weld metal and good bending performance of the welded joint.
(2)金属炭酸塩、Si、Ti含有量を適量にし、鋼心線への被覆率を適正にすると低温での溶接金属の靭性を向上できること。 (2) The toughness of the weld metal at low temperatures can be improved by adjusting the metal carbonate, Si, and Ti content and the coverage rate of the steel core wire.
(3)溶接作業性に関するアークの安定化及びスパッタ発生量の低減には、Si、Ti、Ti酸化物 のTiO2換算値 、金属炭酸塩、金属弗化物、及びNa酸化物、Na弗化物、K酸化物及びK弗化物の1種または2種以上の合計を適量にすることで調整可能なこと。 (3) In order to stabilize the arc and reduce the amount of spatter generated with respect to welding workability, the amount of Si, Ti, Ti oxide (converted into TiO2 ) , metal carbonate, metal fluoride, and one or a total of two or more of Na oxide, Na fluoride, K oxide, and K fluoride can be adjusted to an appropriate amount.
(4)ビード形状及びビード外観はSi酸化物 のSiO2換算値 、Ti酸化物 のTiO2換算値 、金属炭酸塩、金属弗化物、及びMg酸化物のMgO換算値の合計の含有量を適量にすることで改善できること。 (4) The bead shape and bead appearance can be improved by adjusting the total content of silicon oxide ( SiO2 equivalent), titanium oxide ( TiO2 equivalent), metal carbonates, metal fluorides, and magnesium oxide (MgO equivalent) to appropriate amounts.
(5)スラグ剥離性及び被包性はSi酸化物 のSiO2換算値 、金属炭酸塩、金属弗化物及びAl酸化物のAl2O3換算値の合計量を適量にすることで改善できること。 (5) The slag removability and encapsulation properties can be improved by adjusting the total amount of silicon oxide ( SiO2 equivalent), metal carbonate, metal fluoride, and aluminum oxide ( Al2O3 equivalent ) to an appropriate amount.
(6)溶接棒自体が赤熱する棒焼けを防止するには、Feの含有量を適量にすることで、溶接棒の保護筒の片溶けを防止するには金属弗化物及びFeの含有量を適量にすることで、被覆剤の塗装性等の溶接棒の生産性はNa酸化物、Na弗化物、K酸化物及びK弗化物の1種または2種以上の合計量を適量にすることで改善できること。 (6) Rod burn, where the welding rod itself becomes red hot, can be prevented by adjusting the Fe content to an appropriate amount, one-sided melting of the protective tube of the welding rod can be prevented by adjusting the metal fluoride and Fe content to an appropriate amount, and productivity of the welding rod, such as the paintability of the coating agent, can be improved by adjusting the total amount of one or more of Na oxide, Na fluoride, K oxide, and K fluoride to an appropriate amount.
(7)Ca酸化物のCaO換算値の合計を適量にすることで、アークの安定化及びスパッタ発生量の低減がより改善でき、Zr酸化物のZrO2換算値の合計を適量にすることで、ビード形状及びビード外観がより改善できること。 (7) By setting the total amount of Ca oxides in terms of CaO to an appropriate amount, arc stabilization and reduction in the amount of spatter generation can be further improved, and by setting the total amount of Zr oxides in terms of ZrO2 to an appropriate amount, the bead shape and bead appearance can be further improved.
以下、本発明における鉄粉低水素系被覆アーク溶接棒について、被覆剤中の各組成数値範囲の限定理由について詳細に説明する。なお、鉄粉低水素系被覆アーク溶接棒の被覆剤中の各成分組成における含有率は、被覆剤全質量に対する質量%で表すこととし、その質量%を表すときには単に%と記載する。 The reasons for limiting the range of each composition in the coating of the low-hydrogen iron powder covered metal arc welding electrode of the present invention will be explained in detail below. Note that the content of each component in the coating of the low-hydrogen iron powder covered metal arc welding electrode is expressed as mass% relative to the total mass of the coating, and when expressing the mass%, it is simply written as %.
[被覆率:溶接棒全質量に対する質量%で30~45%]
被覆剤の鋼心線の外周への被覆率は、溶接時の耐シールド性に大きく影響する。被覆率が鉄粉低水素系被覆アーク溶接棒全質量に対する被覆剤の質量%(以下、単に%という。)で30%未満では、被覆剤自体が少なくなってシールド不足となり、溶接金属中のN含有量が増加して溶接金属の靱性が低下する。一方、被覆剤の被覆率が45%を超えると、スラグ量が増えすぎてアークが不安定になる。従って、被覆率は30~45%とする。
[Covering rate: 30-45% by mass relative to the total mass of the welding rod]
The coverage rate of the coating material on the outer circumference of the steel core wire has a large effect on the shielding resistance during welding. If the coverage rate is less than 30% by mass of the coating material relative to the total mass of the iron powder low hydrogen type covered metal arc welding electrode (hereinafter simply referred to as %), the coating material itself becomes less, resulting in insufficient shielding, and the N content in the weld metal increases, reducing the toughness of the weld metal. On the other hand, if the coverage rate of the coating material exceeds 45%, the amount of slag increases too much and the arc becomes unstable. Therefore, the coverage rate is set to 30 to 45%.
[Mn:3.0~6.0%]
Mnは、金属Mn、Fe-Mn、Fe-Si-Mn等から添加され、溶接金属の脱酸剤として必要な元素であり、溶接金属組織を微細化して溶接金属の低温靱性及び強度を高める効果がある。Mnが3.0%未満では、溶接金属の強度及び低温靭性が低下する。また、Mnが3.0%未満では、脱酸不足となって溶接金属中にブローホールが発生しやすくなる。一方、Mnが6.0%を超えると、溶接金属の強度が過剰に高くなり、靭性が低下する。従って、Mnは3.0~6.0%とする。
[Mn: 3.0 to 6.0%]
Mn is added from metal Mn, Fe-Mn, Fe-Si-Mn, etc., and is an element necessary as a deoxidizer for the weld metal, and has the effect of refining the weld metal structure and increasing the low-temperature toughness and strength of the weld metal. If Mn is less than 3.0%, the strength and low-temperature toughness of the weld metal decrease. Also, if Mn is less than 3.0%, deoxidation is insufficient and blowholes are likely to occur in the weld metal. On the other hand, if Mn exceeds 6.0%, the strength of the weld metal becomes excessively high and the toughness decreases. Therefore, Mn is set to 3.0 to 6.0%.
[Ni:3.5~7.5%]
Niは、金属Niから添加され、溶接金属の強度、低温靭性を向上させる効果がある。Niが3.5%未満では、溶接金属の強度及び低温靭性が低下する。一方、Niが7.5%を超えると、溶接金属の強度が過剰に高くなる。従って、Niは3.5~7.5%とする。
[Ni: 3.5-7.5%]
Ni is added from metallic Ni and has the effect of improving the strength and low-temperature toughness of the weld metal. If Ni is less than 3.5%, the strength and low-temperature toughness of the weld metal decrease. On the other hand, if Ni exceeds 7.5%, the strength of the weld metal becomes excessively high. Therefore, Ni is set to 3.5 to 7.5%.
[Mo:0.3~1.3%]
Moは、金属Mo、Fe-Mo等から添加され、溶接金属の強度をより向上させる効果がある。Moが0.3%未満では、溶接金属の強度が低下する。一方、Moが1.3%を超えると、溶接金属の強度が過剰に高くなり、靭性が低下する。従って、Moは0.3~1.3%とする。
[Mo: 0.3-1.3%]
Mo is added from metal Mo, Fe-Mo, etc., and has the effect of further improving the strength of the weld metal. If Mo is less than 0.3%, the strength of the weld metal decreases. On the other hand, if Mo exceeds 1.3%, the strength of the weld metal becomes excessively high and the toughness decreases. Therefore, Mo is set to 0.3 to 1.3%.
[Cr:0.2~1.0%]
Crは、金属Cr、Fe-Cr等から添加され、溶接金属の強度をより向上させる効果がある。Crが0.2%未満では、溶接金属の強度及が低下する。一方、Crが1.0%を超えると、溶接金属の強度が過剰に高くなり、靭性が低下する。従って、Crは0.2~1.0%とする。
[Cr: 0.2-1.0%]
Cr is added from metallic Cr, Fe-Cr, etc., and has the effect of further improving the strength of the weld metal. If Cr is less than 0.2%, the strength of the weld metal decreases. On the other hand, if Cr exceeds 1.0%, the strength of the weld metal becomes excessively high and the toughness decreases. Therefore, Cr is set to 0.2-1.0%.
[Si:2.0~5.0%]
Siは、金属Si、Fe-Si、Fe-Si-Mn等から添加され、溶接金属の脱酸を目的として使用される。Siが2.0%未満では、脱酸不足となって溶接金属中にブローホールが発生しやすくなり、アークも不安定となる。一方、Siが5.0%を超えると、溶接金属の粒界に低融点酸化物を析出させ、溶接金属の低温靱性が低下する。従って、Siは2.0~5.0%とする。
[Si: 2.0 to 5.0%]
Silicon is added from metal silicon, Fe-Si, Fe-Si-Mn, etc., and is used for the purpose of deoxidizing the weld metal. If the silicon content is less than 2.0%, deoxidation is insufficient, making blowholes more likely to occur in the weld metal and making the arc unstable. On the other hand, if the silicon content exceeds 5.0%, low-melting-point oxides are precipitated at the grain boundaries of the weld metal, reducing the low-temperature toughness of the weld metal. Therefore, the silicon content is set to 2.0-5.0%.
[Si酸化物のSiO2換算値の合計:3.5~7.5%]
Si酸化物は、珪砂、ジルコンサンド、カリ長石、珪酸ナトリウムや珪酸カリウム等の水ガラスの固質分、珪灰石等から添加され、溶融スラグの粘性を高め、適切な粘性のスラグを確保してビード形状を良好にする効果がある。Si酸化物のSiO2換算値 が3.5%未満では、溶融スラグの粘性が低くなり、ビード形状が不良となる。一方、Si酸化物のSiO2換算値が7.5%を超えると、スラグがガラス状になり、スラグ剥離性が不良になる。従って、Si酸化物のSiO2換算値は3.5~7.5%とする。
[Total of Si oxides converted into SiO2 : 3.5 to 7.5%]
Silicon oxide is added from silica sand, zircon sand, potassium feldspar, solid components of water glass such as sodium silicate and potassium silicate, wollastonite, etc., and has the effect of increasing the viscosity of the molten slag, ensuring slag with appropriate viscosity, and improving the bead shape. If the SiO2 equivalent value of silicon oxide is less than 3.5%, the viscosity of the molten slag will be low and the bead shape will be poor. On the other hand, if the SiO2 equivalent value of silicon oxide exceeds 7.5%, the slag will become glassy and the slag removability will be poor. Therefore, the SiO2 equivalent value of silicon oxide is set to 3.5 to 7.5%.
[Ti:0.2~1.5%]
Tiは、金属Ti、Fe-Ti等から添加され、脱酸剤として有効であると同時に、アークの電位傾度を低下させてアークを安定化させる効果がある。さらに、溶接金属組織を微細化して溶接金属の低温靭性を向上させる効果がある。Tiが0.2%未満では、その効果が得られず、アークが不安定となる。またTiが0.2%未満では、溶接金属中に酸素量が多くなり、溶接金属のミクロ組織が微細化されないので、溶接金属の低温靭性が低下する。一方、Tiが1.5%を超えると、溶接金属中のTi酸化物の析出が増加し、溶接金属の低温靱性が低下する。従って、Tiは0.2~1.5%とする。
[Ti: 0.2 to 1.5%]
Ti is added from metallic Ti, Fe-Ti, etc., and is effective as a deoxidizer, and at the same time, has the effect of lowering the potential gradient of the arc and stabilizing the arc. In addition, it has the effect of refining the weld metal structure and improving the low-temperature toughness of the weld metal. If Ti is less than 0.2%, this effect cannot be obtained and the arc becomes unstable. Also, if Ti is less than 0.2%, the amount of oxygen in the weld metal increases and the microstructure of the weld metal is not refined, so that the low-temperature toughness of the weld metal decreases. On the other hand, if Ti exceeds 1.5%, the precipitation of Ti oxide in the weld metal increases, and the low-temperature toughness of the weld metal decreases. Therefore, Ti is set to 0.2 to 1.5%.
[Ti酸化物のTiO2換算値の合計:1.0~5.0%]
Ti酸化物は、ルチール、酸化チタン、チタンスラグ、チタン酸カルシウム等から添加され、アークを安定にし、溶融スラグの粘性を調整してビード形状を良好にする効果がある。Ti酸化物のTiO2換算値が1.0%未満であると、アークが不安定となり、ビード形状が不良になる。一方、Ti酸化物 のTiO2換算値 が5.0%を超えると、溶融スラグの粘性が高くなってスラグの流動性が悪くなるので、ビード形状が凸状となる。従って、Ti酸化物のTiO2換算値は1.0~5.0%とする。
[Total of Ti oxides converted into TiO2 : 1.0 to 5.0%]
Ti oxide is added from rutile, titanium oxide, titanium slag, calcium titanate, etc., and has the effect of stabilizing the arc and adjusting the viscosity of the molten slag to improve the bead shape. If the TiO2 equivalent of Ti oxide is less than 1.0%, the arc becomes unstable and the bead shape becomes poor. On the other hand, if the TiO2 equivalent of Ti oxide exceeds 5.0%, the viscosity of the molten slag increases and the fluidity of the slag deteriorates, resulting in a convex bead shape. Therefore, the TiO2 equivalent of Ti oxide is set to 1.0 to 5.0%.
[金属炭酸塩の一種或いは二種以上の合計:25~45%]
金属炭酸塩は、炭酸カルシウム、炭酸マグネシウム、炭酸バリウム等から添加され、アークの熱で分解してCO2ガスを発生し、溶接金属を大気から保護する効果がある。金属炭酸塩の一種或いは二種以上の合計が25%未満では、シールド効果が不足し、ブローホールが発生しやすくなる。また、金属炭酸塩の一種或いは二種以上の合計が25%未満では、溶接金属中に大気中の窒素が混入し、低温靱性が低下する。一方、金属炭酸塩の一種或いは二種以上の合計が45%を超えると、アークが不安定となってビード形状が凸状になり、スラグ剥離性も悪くなる。従って、金属炭酸塩の一種或いは二種以上の合計は25~45%とする。
[One or more metal carbonates in total: 25-45%]
Metal carbonates are added from calcium carbonate, magnesium carbonate, barium carbonate, etc., and decompose with the heat of the arc to generate CO2 gas, which has the effect of protecting the weld metal from the atmosphere. If the total of one or more metal carbonates is less than 25%, the shielding effect is insufficient and blowholes are likely to occur. If the total of one or more metal carbonates is less than 25%, nitrogen from the atmosphere is mixed into the weld metal, reducing low-temperature toughness. On the other hand, if the total of one or more metal carbonates exceeds 45%, the arc becomes unstable, the bead shape becomes convex, and slag removability is also poor. Therefore, the total of one or more metal carbonates is set to 25-45%.
[金属弗化物の一種或いは二種以上の合計:5~15%]
金属弗化物は、蛍石、弗化マグネシウム、弗化アルミニウム、弗化リチウム、弗化ナトリウム、珪弗化カリウム等から添加され、溶融スラグの流動性を調整してビード外観を良好にする効果がある。金属弗化物の一種或いは二種以上の合計が5%未満では、溶融スラグの流動性が悪くなりスラグ被包性が悪くなってビード外観が不良になる。一方、金属弗化物の一種或いは二種以上の合計が15%を超えると、被覆筒の形状が不完全となって片溶け状態となり、アークが不安定となる。従って、金属弗化物の一種或いは二種以上の合計は5~15%とする。
[Metal fluorides (one or more): 5-15%]
Metal fluorides are added from fluorite, magnesium fluoride, aluminum fluoride, lithium fluoride, sodium fluoride, potassium silicofluoride, etc., and have the effect of adjusting the fluidity of the molten slag and improving the bead appearance. If the total content of one or more metal fluorides is less than 5%, the fluidity of the molten slag is poor, the slag encapsulation is poor, and the bead appearance is poor. On the other hand, if the total content of one or more metal fluorides exceeds 15%, the shape of the covering tube becomes incomplete, resulting in a one-sided melting state and an unstable arc. Therefore, the total content of one or more metal fluorides is set to 5-15%.
[Al酸化物のAl2O3換算値の合計:2.0%以下]
Al酸化物は、アルミナ、カリ長石等から添加され、アークを安定させるとともにビード形状を良好にする効果がある。しかし、Al酸化物のAl2O3の合計が2.0%を超えると、スラグがガラス状となってスラグ剥離性が不良になる。従って、Al酸化物のAl2O3の合計は2.0%以下とする。
[Total of Al oxide converted into Al 2 O 3 : 2.0% or less]
Aluminum oxide is added from alumina, potassium feldspar, etc., and has the effect of stabilizing the arc and improving the bead shape. However, if the total content of aluminum oxide ( Al2O3 ) exceeds 2.0%, the slag becomes glassy and the slag removability becomes poor. Therefore, the total content of aluminum oxide ( Al2O3 ) is set to 2.0% or less.
[Mg酸化物のMgO換算値の合計:0.8%以下]
Mg酸化物は、酸化マグネシウム、マグネシアクリンカー等から添加され、耐熱性に優れており、被覆剤の片溶けを抑制する効果がある。しかし、Mg酸化物のMgO換算値の合計が0.8%を超えると、溶融スラグの粘性が高くなるので、ビード形状が凸状となる。従って、Mg酸化物のMgO換算値の合計は0.8%以下とする。
[Total of Mg oxides converted into MgO: 0.8% or less]
Mg oxide is added from magnesium oxide, magnesia clinker, etc., and has excellent heat resistance and is effective in suppressing the one-sided melting of the coating material. However, if the total of Mg oxide converted into MgO exceeds 0.8%, the viscosity of the molten slag increases, and the bead shape becomes convex. Therefore, the total of Mg oxide converted into MgO is set to 0.8% or less.
[Na酸化物、Na弗化物、K酸化物及びK弗化物の1種または2種以上の合計:Na換算値とK換算値の合計で1.5~3.0%]
Naは、珪酸ナトリウム等の水ガラスの固質分を始めとするNa酸化物や弗化ナトリウム等を始めとするNa弗化物から添加され、また、Kは、珪酸カリウム等の水ガラスの固質分やカリ長石等を始めとするK酸化物、珪弗化カリウム等を始めとするK弗化物から添加され、溶接棒製造時の塗装性及び溶接時のアークの安定性を向上する効果がある。Na酸化物、Na弗化物、K酸化物及びK弗化物の1種または2種以上の合計が、Na換算値とK換算値の合計で1.5%未満では、アークが不安定になる。また、Na換算値とK換算値の合計が1.5%未満では、生産時の塗装性が悪くなるとともに、溶接棒製造時に被覆剤表面に割れが生じやすくなるなど被覆アーク溶接棒の生産性が低下する。一方、Na換算値とK換算値の合計が3.0%を超えると、アークの吹き付けが強くなり、スパッタ発生量が多くなる。従って、Na酸化物、Na弗化物、K酸化物及びK弗化物の1種または2種以上の合計は、Na換算値とK換算値の合計で1.5~3.0%とする。なお、Na換算値、K換算値は0%を含む。
[Total of one or more of Na oxide, Na fluoride, K oxide and K fluoride: 1.5 to 3.0% in terms of Na and K]
Na is added from Na oxides such as sodium silicate and other solid components of water glass, and Na fluorides such as sodium fluoride, and K is added from potassium silicate and other solid components of water glass, K oxides such as potassium feldspar, and K fluorides such as potassium silicofluoride, and these have the effect of improving the paintability during the manufacture of the welding rod and the stability of the arc during welding. If the total of one or more of Na oxides, Na fluorides, K oxides, and K fluorides is less than 1.5% in terms of Na and K, the arc becomes unstable. If the total of Na and K is less than 1.5%, the paintability during production is poor, and cracks are likely to occur on the coating surface during the manufacture of the welding rod, thereby reducing the productivity of the covered arc welding rod. On the other hand, if the total of Na and K exceeds 3.0%, the arc blow becomes strong and the amount of spatter generation increases. Therefore, the total content of one or more of Na oxide, Na fluoride, K oxide and K fluoride is 1.5 to 3.0% in terms of Na and K. The Na and K values include 0%.
[Mn、Ni、Mo及びCrが式(1)で150~300]
2.3×[Mn]+38.5×[Ni]+4.2×[Mo]+2.1×[Cr]…式(1)(但し、[ ]は、各成分の被覆剤全質量に対する質量%を示す)
[Mn, Ni, Mo and Cr are 150 to 300 in formula (1)]
2.3 × [Mn] + 38.5 × [Ni] + 4.2 × [Mo] + 2.1 × [Cr] ... formula (1) (where [ ] indicates the mass% of each component with respect to the total mass of the coating agent)
上述したMn、Ni、Mo及びCrにおいて、式(1)で得られる値を適正とすることによって、溶接継手の良好な曲げ性能が得られる。式(1)の値が150未満では、良好な溶接継手の曲げ性能が得られない。一方、式(1)の値が300を超えると溶接後のオーステナイト組織が過剰になり、曲げ性能が劣化する。従って、式(1)の値は150~300とする。 By optimizing the values obtained by formula (1) for the above-mentioned Mn, Ni, Mo, and Cr, good bending performance of the welded joint can be obtained. If the value of formula (1) is less than 150, good bending performance of the welded joint cannot be obtained. On the other hand, if the value of formula (1) exceeds 300, the austenitic structure after welding becomes excessive, and bending performance deteriorates. Therefore, the value of formula (1) is set to 150 to 300.
[Fe:20~30%]
Feは、鉄粉やFe-Mn、Fe-Moといった鉄合金粉や鉄酸化物から添加され、アークの電位傾度を低下させてアーク長を短くして被覆剤の片溶けを防止させる効果があり、特に直流電源を用いた溶接において最も重要な原材料である。Feが20%未満では、アーク長が長くなって被覆剤の片溶けが発生しやすくなる。一方、Feが30%を超えると、熱伝導性が高くなり被覆アーク溶接棒による溶接では溶接後半になると被覆アーク溶接棒自体が赤熱(以下、棒焼けという。)してしまい、溶接が困難となる。従って、Feは20~30%とする。
[Fe:20-30%]
Fe is added from iron powder, iron alloy powder such as Fe-Mn and Fe-Mo, or iron oxide, and has the effect of reducing the potential gradient of the arc, shortening the arc length, and preventing one-sided melting of the coating material, and is the most important raw material, especially in welding using a DC power source. If Fe is less than 20%, the arc length becomes long and one-sided melting of the coating material is likely to occur. On the other hand, if Fe exceeds 30%, the thermal conductivity becomes high, and in welding with a covered metal arc welding rod, the covered metal arc welding rod itself becomes red hot (hereinafter referred to as rod burn) in the latter half of welding, making welding difficult. Therefore, Fe is set to 20-30%.
[Ca酸化物のCaO換算値の合計:0.5%以下]
Ca酸化物は、チタン酸カルシウム、珪灰石等から添加され、アークを安定化させてスパッタ発生の低減に効果がある。Ca酸化物のCaO換算値の合計が0.5%を超えると、アークが弱くなって不安定になり、融合不良等の溶接欠陥が発生しやすくなる。従って、Ca酸化物のCaO換算値の合計は0.5%とする。
[Total of Ca oxides converted into CaO: 0.5% or less]
Ca oxide is added from calcium titanate, wollastonite, etc., and is effective in stabilizing the arc and reducing spatter generation. If the total of Ca oxide converted into CaO exceeds 0.5%, the arc becomes weak and unstable, and welding defects such as poor fusion are likely to occur. Therefore, the total of Ca oxide converted into CaO is set to 0.5%.
[Zr酸化物のZrO2換算値の合計:1.5%以下]
Zr酸化物は、ジルコンサンド、ジルコニア等から添加され、融点が2700℃と高く、被覆剤及び鋼心線が過熱した際も安定した耐火性を有し、被覆剤の片溶けを抑制する上で有効である。Zr酸化物のZrO2換算値の合計が1.5%を超えると、溶融スラグの粘性が高くなってスラグの流動性が悪くなり、ビード形状が凸状となる。従って、Zr酸化物のZrO2換算値の合計は1.5%以下とする。
[Total of Zr oxide converted into ZrO2 : 1.5% or less]
Zr oxide is added from zircon sand, zirconia, etc., and has a high melting point of 2700°C, and has stable fire resistance even when the coating material and steel core wire are overheated, and is effective in suppressing one-sided melting of the coating material. If the total of Zr oxide converted into ZrO2 exceeds 1.5%, the viscosity of the molten slag increases, the fluidity of the slag deteriorates, and the bead shape becomes convex. Therefore, the total of Zr oxide converted into ZrO2 is set to 1.5% or less.
なお、本発明の鉄粉低水素系被覆アーク溶接棒の被覆剤の残部は、塗装剤と合金粉とに含まれる不純物である。塗装剤は、ヘクトライト、マイカ等が用いられる。合金粉に含まれる不純物はP、S、Cu、Nb、V、Bなどが挙げられ、特にP及びSは共に低融点の化合物を生成して溶接金属の靭性を低下させるので、不純物の合計は1.0%以下に調整する。 The remainder of the coating material in the iron powder low hydrogen covered metal arc welding electrode of the present invention is impurities contained in the paint and alloy powder. Hectorite, mica, etc. are used as the paint material. Impurities contained in the alloy powder include P, S, Cu, Nb, V, B, etc., and P and S in particular both form compounds with low melting points that reduce the toughness of the weld metal, so the total amount of impurities is adjusted to 1.0% or less.
また、使用する鋼心線は、JIS G3523:1980 SWY11を用いることが好ましいが、SWY11でなくても良い。鋼心線のCは0.08%以下であることが好ましく、強度を調整するために被覆剤からもCを適正に調整できる。鋼心線のPは靭性を低下させるので0.010%以下、Sはスラグの流動性を悪くするので0.010%以下であることが好ましい。 The steel core wire used is preferably JIS G3523:1980 SWY11, but does not have to be SWY11. The C content of the steel core wire is preferably 0.08% or less, and the C content can be appropriately adjusted from the coating material to adjust the strength. P in the steel core wire reduces toughness, so it is preferable that it is 0.010% or less, and S reduces the fluidity of the slag, so it is preferable that it is 0.010% or less.
以下、実施例により本発明の効果を具体的に説明する。 The effects of the present invention will be specifically explained below using examples.
直径4.0mm、長さ400mmのJIS G3523:1980 SWY11の鋼心線(C:0.08%、Si:0.02%、Mn:0.46%、P:0.009%、S:0.006%)に、表1に示す成分組成の被覆剤を表1及び表2に示す被覆率で塗装した後、乾燥させて各種鉄粉低水素系被覆アーク溶接棒を試作した。この際、被覆剤の成分組成はJIS K0116:2014に記載のICP発光分光分析方法を用いて調査した。試料は試作溶接棒の被覆剤を剥がして回収し、粉砕した粉末試料とした。粉末試料の分解には、酸分解法又はアルカリ融解法を用いた。溶液の一部を噴霧してICP発光分光分析装置のアルゴンプラズマ中に導入し、定量成分の分析線の発光強度又は定量成分の分析線の発光強度の内標準元素の発光強度に対する比を測定した。得られた発光強度から検量線法を用いて試料溶液中の測定対象元素の濃度を求めた。また、SiとSiO2など、金属系と酸化物系の定量分析にはX線回折分析法を用いた。例えば被覆剤中のSi量を、ICP発光分光分析方法を用いて特定し、同じ被覆剤を用いてX線回折分析法で金属系Siと酸化物系Siを測定し、それぞれの定量分析値を求めた。なお、分析精度を高めるために、被覆剤はメノウ乳鉢などで10μm以下の細粒に粉砕することが望ましい。試料充填の手順は、10cm角、厚さ5mm程度の厚みのある平らなガラス板の上にガラス試料板をおき、深さ0.5mm程度の溝にガラス板で抑え、試料板の表面と試料面が同一面になるように仕上げてX線回折分析装置で分析を行った。 A JIS G3523:1980 SWY11 steel core wire (C: 0.08%, Si: 0.02%, Mn: 0.46%, P: 0.009%, S: 0.006%) having a diameter of 4.0 mm and a length of 400 mm was coated with a coating agent having the composition shown in Table 1 at the coverage shown in Tables 1 and 2, and then dried to produce various iron powder low hydrogen type covered metal arc welding rods. In this case, the composition of the coating agent was investigated using the ICP optical emission spectrometry method described in JIS K0116 :2014. The coating agent of the prototype welding rod was peeled off, recovered, and pulverized to obtain a powder sample. The powder sample was decomposed using an acid decomposition method or an alkali fusion method. A part of the solution was sprayed and introduced into the argon plasma of an ICP optical emission spectrometry device, and the emission intensity of the analytical line of the quantitative component or the ratio of the emission intensity of the analytical line of the quantitative component to the emission intensity of the internal standard element was measured. The concentration of the element to be measured in the sample solution was determined from the obtained emission intensity using the calibration curve method. X-ray diffraction analysis was also used for quantitative analysis of metals and oxides, such as Si and SiO2 . For example, the amount of Si in the coating agent was specified using ICP emission spectroscopy, and the metal Si and oxide Si were measured using the same coating agent by X-ray diffraction analysis to obtain the quantitative analysis values for each. In addition, in order to improve the analytical accuracy, it is desirable to crush the coating agent into fine particles of 10 μm or less using an agate mortar or the like. The procedure for filling the sample was to place a glass sample plate on a flat glass plate with a size of 10 cm square and a thickness of about 5 mm, hold it down with a glass plate in a groove with a depth of about 0.5 mm, finish it so that the surface of the sample plate and the sample surface are on the same plane, and perform the analysis with an X-ray diffraction analysis device.
上記の各種試作溶接棒を用い、表3に示す成分の板厚20mmの鋼板を開先角度:20°、ルートギャップ:16mmの裏当金付開先とし、直流電源を用いて溶接電流:170A、溶接入熱:19kJ/cm、予熱・パス間温度:95~120℃の条件で溶着金属試験体を作製した。さらに、表3に示す成分の板厚20mmの鋼板を開先角度:60℃、ルートフェイス:2mm、ルートギャップ:2.5mmの突合せV型開先とし、直流電源を用いて溶接電流:80~140A、溶接入熱:24kJ/cm、予熱・パス間温度:95~120℃の条件で溶接、裏はつり加工を行い、同様の条件にて溶接し、溶接継手を作製した。 Using the above various prototype welding rods, weld metal test specimens were prepared by forming a 20 mm thick steel plate with the composition shown in Table 3 into a backed groove with a groove angle of 20° and a root gap of 16 mm, and using a DC power source with a welding current of 170 A, welding heat input of 19 kJ/cm, and preheat/interpass temperature of 95-120°C. Furthermore, a 20 mm thick steel plate with the composition shown in Table 3 was formed into a butt V-groove with a groove angle of 60°C, root face: 2 mm, and root gap: 2.5 mm, and welded and back-ground using a DC power source with a welding current of 80-140 A, welding heat input of 24 kJ/cm, and preheat/interpass temperature of 95-120°C, and welded under the same conditions to prepare welded joints.
溶接作業性の評価は、各試作溶接棒を用い、上記溶接時にアーク安定性、スパッタ発生量、ビード形状・ビード外観、スラグ剥離性、片溶け及び棒焼けの有無を目視にて調査した。溶接終了後、AWS A5.5に準じてX線透過試験を行い、溶接欠陥の有無を調査した。溶着金属試験体の板厚中央から引張試験片(AWS B4.0:2007)及びVノッチ衝撃試験片(AWS B4.0:2007)を採取した。引張試験は、引張強さが810~920MPaを良好、靱性の評価は、試験温度-50℃でシャルピー衝撃試験を実施し、吸収エネルギーの5回のうち、最低値と最高値を除いた3回の平均値が40J以上を良好とした。曲げ性能の評価は溶接継手から曲げ試験片(AWS B4.0:2007)を採取し、割れ長さの合計が3.2mm以下を合格とし、割れ長さの合計が3.2mm超を不合格とした。それらの試験結果を表5にまとめて示す。 Welding workability was evaluated using each prototype welding rod, and arc stability, amount of spatter generation, bead shape and appearance, slag removability, and the presence or absence of one-sided melting and rod burn were visually inspected during the above welding. After welding was completed, an X-ray transmission test was performed in accordance with AWS A5.5 to check for the presence or absence of welding defects. Tensile test pieces (AWS B4.0:2007) and V-notch impact test pieces (AWS B4.0:2007) were taken from the center of the plate thickness of the weld metal test pieces. In the tensile test, a tensile strength of 810 to 920 MPa was considered good, and toughness was evaluated by performing a Charpy impact test at a test temperature of -50°C, and an average of 40 J or more for the three out of five absorbed energy tests, excluding the lowest and highest values, was considered good. To evaluate bending performance, bending test pieces (AWS B4.0:2007) were taken from the welded joints, and a total crack length of 3.2 mm or less was considered to be pass, while a total crack length of more than 3.2 mm was considered to be fail. The test results are summarized in Table 5.
[溶接作業性]
(アーク安定性)
溶接時にアークが安定しており、アークが消失しなかった場合を良好、一度でもアークが消失した場合を不良とした。
[Welding workability]
(Arc stability)
If the arc was stable during welding and did not disappear, it was rated as good, and if the arc disappeared even once, it was rated as poor.
(スパッタ発生量)
溶接時のスパッタ発生量が少ないことが好ましい。具体的には、銅製の捕集箱を用いて、1分間溶接した際に発生するスパッタの重量を測定することにより、単時間当たりの値(g/min)を求めた。なお、スパッタの測定は、表4に示す溶接条件で5回測定した平均値とし、2.0g/min以下を良好とした。
(Amount of spatter generated)
It is preferable that the amount of spatter generated during welding is small. Specifically, the weight of spatter generated during one minute of welding was measured using a copper collection box to determine the value per unit time (g/min). The spatter was measured five times under the welding conditions shown in Table 4, and the average value was determined, with 2.0 g/min or less being considered good.
(ビード形状・ビード外観)
溶着金属のビード波形が均一で乱れが無く、手直しが必要なアンダーカットおよびオーバーラップが発生しないことが好ましい。溶着金属の余盛高さ及びビード幅の均一性に優れたビード形状を有することが好ましい。具体的には、溶着金属のビード表面において、ビード波形に乱れがある場合及び、手直しが必要なアンダーカットおよびオーバーラップが発生した場合を不良とした。
(Bead shape and appearance)
It is preferable that the bead waveform of the deposited metal is uniform and free of disturbance, and that there is no undercut or overlap that requires rework. It is preferable that the deposited metal has a bead shape with excellent uniformity in the excess height and bead width. Specifically, a case where the bead waveform of the deposited metal is disturbed or where undercut or overlap that requires rework occurs on the bead surface of the deposited metal is determined as defective.
(スラグ剥離性)
溶接後、溶接ビード表面上の凝固スラグを簡単に除去できることが好ましい。溶接後、溶接ビード表面上の凝固スラグをチッピングハンマー(全長300mm、重さ350g)を用いて、持ち手を中心に円弧に軽い力で振り下ろして叩いた時に、スラグに亀裂が入りその後簡単に除去できる場合を良好、スラグに亀裂が入らない場合を不良とした。
(Slag removability)
It is preferable that the solidified slag on the weld bead surface can be easily removed after welding. After welding, the solidified slag on the weld bead surface was struck with a chipping hammer (total length 300 mm, weight 350 g) by swinging it down lightly in an arc around the handle. If the slag cracked and could be easily removed, it was rated as good, and if the slag did not crack, it was rated as poor.
(被覆剤の片溶け)
溶接中に被覆剤の一部が欠けることなくアークが溶接棒と水平に発生し、アーク拡がりが均一で安定していることが好ましい。溶接中に被覆剤の一部が欠け、アークが溶接棒と水平以外の方向に偏向し、アーク拡がりが不均一になる場合を不良とした。
(Partial dissolution of coating material)
It is preferable that the arc is generated parallel to the welding rod without any chipping of the coating material during welding, and that the arc spread is uniform and stable. If part of the coating material is chipped during welding, the arc is deflected in a direction other than parallel to the welding rod, and the arc spread is non-uniform, it is rated as defective.
(棒焼け)
溶接時に赤熱して溶接中に被覆剤が脱落することが無いことが好ましい。溶接時に溶接棒の色が変わらず同じ場合を良好、溶接時に赤熱して溶接棒の色が赤色に変色した場合を不良とした。
(stick burn)
It is preferable that the coating does not fall off during welding because the welding rod becomes red hot. A welding rod that does not change color during welding is rated as good, and a welding rod that becomes red hot and turns red is rated as bad.
[溶接欠陥]
具体的には、AWS A5.5に準じてX線透過試験を行い、溶接金属におけるきずを判定した。きずが無い場合を良好、きずが一つでもある場合を不良とした。
[Welding defects]
Specifically, an X-ray examination was performed in accordance with AWS A5.5 to judge whether there were any defects in the weld metal. A specimen without any defects was rated as good, and a specimen with even one defect was rated as poor.
表1、表2及び表5中の溶接棒No.1~No.13が本発明例、溶接棒No.14~No.28は比較例である。本発明例であるNo.1~No.13は、被覆剤のMn、Ni、Mo、Cr、Si、Si酸化物のSiO2換算値、Ti、Ti酸化物のTiO2換算値、金属炭酸塩、金属弗化物、Al酸化物のAl2O3換算値の合計、Mg酸化物のMgO換算値の合計、Na酸化物、Na弗化物、K酸化物及びK弗化物の1種または2種以上のNa換算値とK換算値の合計、Fe、被覆率がいずれも適量であるので、アーク状態が良好でスパッタ発生量が少なく、保護筒の状態も良好で、棒焼けも発生せず、ビード外観、ビード形状、スラグ剥離性及びスラグ被包性が良好であるなど溶接作業性が良好で、生産性も良好で、溶接欠陥も無く、溶着金属の引張強さ及び吸収エネルギーが良好であり、以下の式(1)の値が適正であったため、溶接金属の曲げ性能も良好で、極めて満足な結果であった。 Welding rods No. 1 to No. 13 in Tables 1, 2 and 5 are examples of the present invention, and welding rods No. 14 to No. 28 are comparative examples. In Example 13, the coating agent had appropriate amounts of Mn, Ni, Mo, Cr, Si, Si oxide in SiO2 equivalent, Ti, Ti oxide in TiO2 equivalent, metal carbonate, metal fluoride, total Al oxide in Al2O3 equivalent, total Mg oxide in MgO equivalent, Na oxide, Na fluoride, total Na and K values of one or more of K oxide and K fluoride, Fe, and coverage, so that the arc condition was good, the amount of spatter generation was small, the condition of the protective tube was good, no rod burn occurred, the bead appearance, bead shape, slag removability and slag encapsulation were good, and so the welding workability was good, the productivity was good, there were no welding defects, and the tensile strength and absorbed energy of the weld metal were good. Since the value of the following formula (1) was appropriate, the bending performance of the weld metal was also good, and the results were extremely satisfactory.
2.3×[Mn]+38.5×[Ni]+4.2×[Mo]+2.1×[Cr]・・・式(1)
但し、[ ]は、各成分の被覆剤全質量に対する質量%を示す。
2.3 × [Mn] + 38.5 × [Ni] + 4.2 × [Mo] + 2.1 × [Cr] ... formula (1)
Here, the brackets [ ] indicate the mass % of each component relative to the total mass of the coating agent.
さらに、No.6、No.10、No.11はCa酸化物のCaO換算値の合計が適量であるので、その他の本発明例よりもアーク状態が良好で、スパッタが少なかった。 In addition, since No. 6, No. 10, and No. 11 have an appropriate total CaO equivalent value of Ca oxide, the arc condition was better than the other inventive examples, and there was less spatter.
また、No.1、No.3、No.12はZr酸化物のZrO2換算値の合計が適量であるので、その他の発明例よりも被覆剤の片溶けが抑制されていた。 In addition, since No. 1, No. 3, and No. 12 have an appropriate total amount of Zr oxide converted into ZrO2 , the one-sided dissolution of the coating material was suppressed more than in the other invention examples.
比較例中、溶接棒No.14は、Mnが多く、Siが少ないので、溶着金属の引張強さが高く、吸収エネルギーが低く、アークが不安定で、ブローホールが発生した。 Among the comparative examples, welding rod No. 14 had a high Mn content and a low Si content, so the tensile strength of the deposited metal was high, the absorbed energy was low, the arc was unstable, and blowholes occurred.
溶接棒No.15は、被覆率が高く、Mnが少なく、Si酸化物のSiO2換算値が少ないので、溶着金属の引張強さが低く、吸収エネルギーが低く、ビード形状が不良で、アークが不安定で、ブローホールが発生した。 Welding rod No. 15 had a high coverage, low Mn, and low SiO2 equivalent value of silicon oxide, so the deposited metal had low tensile strength, low absorbed energy, poor bead shape, unstable arc, and blowholes.
溶接棒No.16は、Niが多く、Al酸化物のAl2O3換算値の合計が多く、Na換算値とK換算値の合計が多いので、溶着金属の引張強さが高く、スラグ剥離性が不良で、アークが強く、スパッタが多かった。さらに、以下の式(1)の値が大きいため、溶接金属の曲げ試験が不合格であった。 Welding rod No. 16 had a large amount of Ni, a large total amount of Al oxide in terms of Al2O3 , and a large total amount of Na and K, so the tensile strength of the weld metal was high, the slag removability was poor, the arc was strong, and there was a lot of spatter. Furthermore, the value of the following formula (1) was large, so the bending test of the weld metal was unsuccessful.
2.3×[Mn]+38.5×[Ni]+4.2×[Mo]+2.1×[Cr]・・・式(1)
但し、[ ]は、各成分の被覆剤全質量に対する質量%を示す。
2.3 × [Mn] + 38.5 × [Ni] + 4.2 × [Mo] + 2.1 × [Cr] ... formula (1)
Here, the brackets [ ] indicate the mass % of each component relative to the total mass of the coating agent.
溶接棒No.17は、Niが少なく、金属炭酸塩の合計が多いので、溶着金属の引張強さ及び吸収エネルギーが低く、スラグ剥離性が不良で、ビード形状が凸になり、アークが不安定であった。さらに、以下の式(1)の値が小さいため、溶接金属の曲げ試験が不合格であった。 Welding rod No. 17 had a low Ni content and a high total metal carbonate content, so the tensile strength and absorbed energy of the weld metal were low, the slag removability was poor, the bead shape was convex, and the arc was unstable. Furthermore, because the value of the following formula (1) was small, the weld metal failed the bending test.
2.3×[Mn]+38.5×[Ni]+4.2×[Mo]+2.1×[Cr]・・・式(1)
但し、[ ]は、各成分の被覆剤全質量に対する質量%を示す。
2.3 × [Mn] + 38.5 × [Ni] + 4.2 × [Mo] + 2.1 × [Cr] ... formula (1)
Here, the brackets [ ] indicate the mass % of each component relative to the total mass of the coating agent.
溶接棒No.18は、Moが多く、金属弗化物の合計が多いので、溶着金属の引張強さが高く、吸収エネルギーが低く、アークが不安定で、片溶けが発生した。 Welding rod No. 18 contains a lot of Mo and a large amount of metal fluorides in total, so the tensile strength of the weld metal is high, the absorbed energy is low, the arc is unstable, and one-sided melting occurs.
溶接棒No.19は、Moが少なく、金属弗化物の合計が少ないので、溶着金属の引張強さが低く、スラグ被包性が不良で、ビード外観が不良であった。 Welding rod No. 19 had a low Mo content and a low total metal fluoride content, so the tensile strength of the deposited metal was low, the slag encapsulation was poor, and the bead appearance was poor.
溶接棒No.20は、Crが多く、Ti酸化物のTiO2換算値が少ないので、溶着金属の引張強さが高く、吸収エネルギーが低く、ビード形状が不良で、アークが不安定であった。 Welding rod No. 20 had a large amount of Cr and a small amount of Ti oxide converted into TiO2 , so the tensile strength of the weld metal was high, the absorbed energy was low, the bead shape was poor, and the arc was unstable.
溶接棒No.21は、Crが少なく、Na換算値とK換算値の合計が少ないので、溶着金属の引張強さが低く、アークが不安定で、生産性が不良であった。 Welding rod No. 21 had a low Cr content and a low total Na and K content, so the tensile strength of the deposited metal was low, the arc was unstable, and productivity was poor.
溶接棒No.22は、Siが多く、Feが多いので、吸収エネルギーが低く、棒焼けが発生した。 Welding rod No. 22 has a high Si and Fe content, so it absorbed less energy and rod burn occurred.
溶接棒No.23は、Tiが少なく、Ti酸化物のTiO2換算値が多く、Feが少ないので、吸収エネルギーが低く、ビード形状が凸状であり、アークが不安定で、片溶けが発生した。 Welding rod No. 23 had a small amount of Ti, a large amount of Ti oxide converted into TiO2 , and a small amount of Fe, so that the absorbed energy was low, the bead shape was convex, the arc was unstable, and one-sided melting occurred.
溶接棒No.24は、Si酸化物のSiO2換算値が多く、Tiが多いので、吸収エネルギーが低く、スラグ剥離性が不良であった。さらに、Ca酸化物を添加したが、Ca酸化物のCaO換算値の合計が多かったため、アークが不安定で、融合不良が発生した。 Welding rod No. 24 had a large amount of Si oxide in terms of SiO2 and a large amount of Ti, so the absorbed energy was low and the slag removability was poor. Furthermore, Ca oxide was added, but the total amount of Ca oxide in terms of CaO was high, so the arc was unstable and poor fusion occurred.
溶接棒No.25は、金属炭酸塩の合計が少ないので、吸収エネルギーが低く、ブローホールが発生した。さらに、Zr酸化物を添加したが、Zr酸化物のZrO2換算値の合計が多かったため、ビード形状が凸状であった。 Welding rod No. 25 had a low total amount of metal carbonates, so the absorbed energy was low and blowholes occurred. Furthermore, Zr oxide was added, but the total amount of Zr oxide converted to ZrO2 was high, so the bead shape was convex.
溶接棒No.26は、被覆率が低く、MgO酸化物のMgO換算値の合計が多いので、吸収エネルギーが低く、ビード形状が凸状であった。 Welding rod No. 26 had a low coverage rate and a high total MgO equivalent value of MgO oxide, so the absorbed energy was low and the bead shape was convex.
Claims (3)
被覆剤の被覆率が溶接棒全質量に対する質量%で30~45%であり、
前記被覆剤の組成が被覆剤全質量に対する質量%で、
Mn:3.0~6.0%、
Ni:3.5~7.5%、
Mo:0.3~1.3%、
Cr:0.2~1.0%、
Si:2.0~5.0%、
Si酸化物のSiO2換算値の合計:3.5~7.5%、
Ti:0.2~1.5%、
Ti酸化物のTiO2換算値の合計:1.0~5.0%、
一種或いは二種以上の金属炭酸塩の合計:25~45%、
一種或いは二種以上の金属弗化物の合計:5~15%を含有し、
Al酸化物のAl2O3換算値の合計:2.0%以下、
Mg酸化物のMgO換算値の合計:0.8%以下であり、
Na酸化物、Na弗化物、K酸化物及びK弗化物の1種または2種以上の合計:Na換算値とK換算値の合計で1.5~3.0%を含有し、
かつ、前記Mn、Ni、Mo及びCrが式(1)で150~300であり、
さらにFe:20~30%を含有し、
不純物からなる残部の合計が1.0%以下である被覆剤を塗装してあることを特徴とする鉄粉低水素系被覆アーク溶接棒。
2.3×[Mn]+38.5×[Ni]+4.2×[Mo]+2.1×[Cr]・・・式(1)
但し、[]は、各成分の被覆剤全質量に対する質量%を示す。 In a low-hydrogen iron powder covered metal arc welding electrode for multi-layer welding using a DC power source for 780 MPa class high tensile steel, the steel core wire is coated with a coating material,
The coverage of the coating material is 30 to 45% by mass relative to the total mass of the welding rod;
The composition of the coating agent is expressed as a mass % based on the total mass of the coating agent,
Mn: 3.0 to 6.0%,
Ni: 3.5-7.5%,
Mo: 0.3-1.3%,
Cr: 0.2-1.0%,
Si: 2.0 to 5.0%,
Total of Si oxides converted into SiO2 : 3.5 to 7.5%,
Ti: 0.2 to 1.5%,
Total of Ti oxides converted into TiO2 : 1.0 to 5.0%,
Total of one or more metal carbonates: 25-45%;
One or more metal fluorides in total: 5 to 15%;
The total value of Al oxide calculated as Al2O3 : 2.0% or less,
The total amount of magnesium oxides converted into MgO is 0.8% or less.
One or more of Na oxide, Na fluoride, K oxide, and K fluoride in total: 1.5 to 3.0% in terms of Na and K,
and the Mn, Ni, Mo and Cr are 150 to 300 in formula (1);
Further, Fe: 20 to 30% is contained,
1. An iron powder low hydrogen type covered metal arc welding electrode, characterized in that it is coated with a coating material having a total impurity balance of 1.0% or less.
2.3 × [Mn] + 38.5 × [Ni] + 4.2 × [Mo] + 2.1 × [Cr] ... formula (1)
Here, [ ] indicates the mass % of each component relative to the total mass of the coating agent.
Ca酸化物のCaO換算値の合計:0.5%以下
であることを特徴とする請求項1記載の鉄粉低水素系被覆アーク溶接棒。 The coating agent is, in mass % based on the total mass of the coating agent,
2. The low hydrogen iron powder covered metal arc welding electrode according to claim 1, characterized in that the total amount of Ca oxides calculated as CaO is 0.5% or less.
Zr酸化物のZrO2換算値の合計:1.5%以下
であることを特徴とする請求項1又は請求項2記載の鉄粉低水素系被覆アーク溶接棒。 The coating agent is, in mass % based on the total mass of the coating agent,
3. The low hydrogen iron powder covered metal arc welding electrode according to claim 1, wherein the total amount of Zr oxide calculated as ZrO2 is 1.5% or less.
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| JP2010110817A (en) | 2008-10-11 | 2010-05-20 | Kobe Steel Ltd | Low-hydrogen coated electrode |
| JP2010227968A (en) | 2009-03-27 | 2010-10-14 | Kobe Steel Ltd | Low hydrogen coated arc welding rod |
| JP2014188540A (en) | 2013-03-26 | 2014-10-06 | Nippon Steel & Sumikin Welding Co Ltd | Low hydrogen type covered electrode |
| JP2015128779A (en) | 2014-01-07 | 2015-07-16 | 株式会社神戸製鋼所 | Low hydrogen type covered electrode |
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| JP2010110817A (en) | 2008-10-11 | 2010-05-20 | Kobe Steel Ltd | Low-hydrogen coated electrode |
| JP2010227968A (en) | 2009-03-27 | 2010-10-14 | Kobe Steel Ltd | Low hydrogen coated arc welding rod |
| JP2014188540A (en) | 2013-03-26 | 2014-10-06 | Nippon Steel & Sumikin Welding Co Ltd | Low hydrogen type covered electrode |
| JP2015128779A (en) | 2014-01-07 | 2015-07-16 | 株式会社神戸製鋼所 | Low hydrogen type covered electrode |
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