WO2014051119A1 - 電縫溶接鋼管 - Google Patents
電縫溶接鋼管 Download PDFInfo
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- WO2014051119A1 WO2014051119A1 PCT/JP2013/076422 JP2013076422W WO2014051119A1 WO 2014051119 A1 WO2014051119 A1 WO 2014051119A1 JP 2013076422 W JP2013076422 W JP 2013076422W WO 2014051119 A1 WO2014051119 A1 WO 2014051119A1
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F16—ENGINEERING ELEMENTS AND UNITS; GENERAL MEASURES FOR PRODUCING AND MAINTAINING EFFECTIVE FUNCTIONING OF MACHINES OR INSTALLATIONS; THERMAL INSULATION IN GENERAL
- F16L—PIPES; JOINTS OR FITTINGS FOR PIPES; SUPPORTS FOR PIPES, CABLES OR PROTECTIVE TUBING; MEANS FOR THERMAL INSULATION IN GENERAL
- F16L9/00—Rigid pipes
- F16L9/02—Rigid pipes of metal
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K11/00—Resistance welding; Severing by resistance heating
- B23K11/002—Resistance welding; Severing by resistance heating specially adapted for particular articles or work
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K11/00—Resistance welding; Severing by resistance heating
- B23K11/08—Seam welding not restricted to one of the preceding subgroups
- B23K11/087—Seam welding not restricted to one of the preceding subgroups for rectilinear seams
- B23K11/0873—Seam welding not restricted to one of the preceding subgroups for rectilinear seams of the longitudinal seam of tubes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B23—MACHINE TOOLS; METAL-WORKING NOT OTHERWISE PROVIDED FOR
- B23K—SOLDERING OR UNSOLDERING; WELDING; CLADDING OR PLATING BY SOLDERING OR WELDING; CUTTING BY APPLYING HEAT LOCALLY, e.g. FLAME CUTTING; WORKING BY LASER BEAM
- B23K35/00—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting
- B23K35/22—Rods, electrodes, materials, or media, for use in soldering, welding, or cutting characterised by the composition or nature of the material
- B23K35/38—Selection of media, e.g. special atmospheres for surrounding the working area
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/50—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for welded joints
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/001—Ferrous alloys, e.g. steel alloys containing N
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/005—Ferrous alloys, e.g. steel alloys containing rare earths, i.e. Sc, Y, Lanthanides
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/08—Ferrous alloys, e.g. steel alloys containing nickel
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/16—Ferrous alloys, e.g. steel alloys containing copper
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/26—Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/28—Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/005—Ferrite
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D2211/00—Microstructure comprising significant phases
- C21D2211/008—Martensite
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- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/12—All metal or with adjacent metals
- Y10T428/12292—Workpiece with longitudinal passageway or stopweld material [e.g., for tubular stock, etc.]
Definitions
- the present invention relates to an electric resistance welded steel pipe having excellent low temperature toughness and low yield ratio, which is optimal for uses such as oil and natural gas transportation line pipes.
- the ERW welded steel pipe used for the pipeline is required to be thicker and higher in strength.
- bending and unbending may be applied to the ERW welded steel pipe, so a low yield ratio is required to prevent buckling.
- the yield ratio is an index of durability performance until the material is subjected to a stress larger than the yield stress and yields the material and then buckles and breaks. The lower the yield ratio, the less the steel pipe is buckled.
- the yield ratio (hereinafter also referred to as “YR”) is a value represented by the ratio (YS / TS) of yield stress (hereinafter also referred to as “YS”) and tensile strength (hereinafter also referred to as “TS”).
- YR decreases if the metal structure of the steel material is made of a multiphase structure consisting of a soft phase and a hard phase. Has been.
- Patent Document 1 discloses a low-yield ratio ERW steel pipe in which island-like martensite and retained austenite are generated as the second phase.
- Patent Document 2 discloses a hot rolled steel sheet having a low yield ratio, which is a material for line pipes manufactured by spiral pipe making or UO pipe making.
- the present invention has been made in view of such circumstances, and provides a thick-walled electric-welded steel pipe that can maintain a low yield ratio even when the pipe is formed, and a method for manufacturing the same.
- Nb was added to ensure the strength by precipitating NbC in ferrite.
- Nb increases the yield stress of the hot-rolled steel sheet that is the material of the steel pipe, and as a result, it is difficult to achieve a low yield ratio after pipe forming. It was. Therefore, the present inventors have studied to increase the strength and reduce the yield ratio not by precipitation strengthening but by the hard phase of the second phase.
- ⁇ Dual phase steel undergoes work hardening by introducing dislocations into the soft phase around the hard phase during plastic deformation. Therefore, if the deformation of the hard phase is suppressed, the accumulation of dislocations into the soft phase is promoted, and the work hardening rate can be increased. Accordingly, in the ferrite-martensitic duplex stainless steel, the harder the martensite (hard phase) that is the second phase, the higher the work hardening rate of the ferrite, and the work hardening characteristics of the steel sheet and the steel pipe are improved.
- the present inventors examined in detail the yield ratio exerted by the hard phase of the second phase.
- the cooling after hot rolling is a two-stage cooling in which the cooling rate is changed at 650 ° C., and the coiling temperature after hot rolling is made low so that the hard phase is refined and hardened. And found that the yield ratio can be lowered.
- the present inventors have controlled the hot rolling conditions and reduced the ferrite grain size. As a result, it was found that the deterioration of the toughness of the steel pipe can be suppressed by refining the hard phase after winding.
- the composition of the base material is mass%, C: 0.05 to 0.10%, Mn: 1.00 to 1.60%, Ti: 0.005 to 0.030%, Nb: 0.005% or more and less than 0.035%, and N: 0.001 to 0.008% In addition, Si: 0.01 to 0.60%, and Al: 0.001 to 0.10% One or both of P: 0.02% or less, S: limited to 0.005% or less, and The balance is iron and inevitable impurities, Ceq represented by the following (formula 1) satisfies 0.23 ⁇ Ceq ⁇ 0.38, and An electric resistance welded steel pipe characterized in that the metal structure of the base metal contains 3 to 13% martensite in area ratio, and the balance is ferrite.
- Ceq C + Mn / 6 + (Cr + Mo + V) / 5 + (Ni + Cu) / 15 (Formula 1)
- C, M, Cr, Mo, V, Ni, and Cu in (Expression 1) are values representing the content of each element in mass%.
- the component composition of the base material is further mass%, Ni: 1.0% or less, Cu: 1.0% or less, Cr: 1.0% or less, Mo: 0.5% or less, V: 0.2% or less, One or more of Ca: 0.006% or less and REM: 0.006% or less are contained.
- the composition of the base material is Mn: 1.00 to 1.50%, Si: 0.40% or less, Meet, and 0.23 ⁇ Ceq ⁇ 0.30
- the average value of the equivalent circle diameter of the martensite of the metal structure of the base material is 0.5 to 1.5 ⁇ m, and
- composition of the base material is Nb: 0.005 to 0.020% (3)
- the component composition of the base material is further mass%, Ni: 0.5% or less, Cu: 0.5% or less, Cr: 0.5% or less, Mo: 0.2% or less, V: 0.1% or less,
- the strength level is X60-X70 grade (American Petroleum Institute (API) standard) (the tensile strength of the steel pipe is 520-790 MPa), it has sufficient low temperature toughness, and the yield ratio can be improved even when the pipe is still formed. It is possible to provide an electric resistance welded steel pipe that can be reduced to 90% or less and a method for manufacturing the same.
- API American Petroleum Institute
- FIG. 2A is an optical micrograph of a conventional ERW welded steel pipe having high Nb and high C
- FIG. 2B is an optical micrograph observed after repeller etching
- FIG. 3A is an optical micrograph of an electric resistance welded steel pipe having a composition within the scope of the present invention
- FIG. 3B is an optical micrograph observed after repeller etching.
- the metal structure of the hot-rolled steel sheet as a base material into a multiphase structure composed of a soft phase and a hard phase.
- the soft phase is ferrite and the hard phase is martensite.
- a yield ratio can be reduced by reducing the coiling temperature of hot rolling.
- Martensite can be observed as a whitened phase with an optical microscope if it is subjected to repeller etching. Therefore, the area ratio of martensite can be obtained from the structure photograph.
- FIG. 2 (a) is an optical micrograph of a conventional high-Nb and high-C ERW welded steel pipe with excessive addition of Nb and C
- FIG. 2 (b) is after repeller etching. It is the optical microscope photograph observed.
- FIG. 3A is an optical micrograph of an electric resistance welded steel pipe having a composition within the scope of the present invention
- FIG. 3B is an optical micrograph observed after repeller etching. As can be seen by comparing FIG. 2 (b) and FIG.
- the volume ratio of the retained austenite in FIG. 3B was measured by the X-ray diffraction method. As a result, the volume ratio of retained austenite was 1% or less. If the volume fraction of retained austenite is 1% or less, the properties of the electric resistance welded steel pipe of the present invention are not affected.
- the yield ratio was determined by performing a tensile test and obtaining YS / TS, and expressed as a percentage.
- the result of investigating the relationship between the area ratio of martensite and the yield ratio is shown in FIG. As shown in FIG. 1, when the area ratio of martensite is 3% or more, the yield ratio is 90% or less. Furthermore, when the area ratio of martensite is 8% or more, the yield ratio is drastically lowered, and the yield ratio can be lowered to 80% or less.
- the component of the hot rolled steel sheet which is the material of the ERW steel pipe, is the same as that of the base material of the ERW welded steel pipe.
- “%” represents “mass%”.
- C is a useful element that increases the strength of the steel, increases martensite, hardens the steel, and contributes to a decrease in the yield ratio, so the lower limit is made 0.05%. If the amount of C exceeds 0.10%, the on-site weldability is deteriorated, the area ratio of martensite is increased, the strength becomes too high, and the toughness is deteriorated, so the upper limit is made 0.10%. From the viewpoint of ensuring strength, the C content is preferably 0.06% or more. From the viewpoint of ensuring toughness without excessively increasing the strength, the C content is preferably 0.08% or less.
- Mn is an element that enhances the hardenability of steel and contributes to the formation of martensite.
- 1.00% or more of Mn is added to ensure strength. If Mn is added excessively, the area ratio of martensite increases and the toughness deteriorates, so the upper limit is made 1.60%.
- the Mn content is preferably 1.10% or more, more preferably 1.20% or more.
- the amount of Mn is preferably 1.50% or less, and more preferably 1.40% or less.
- Ti is an element that forms carbonitrides, refines the structure, and contributes to improved toughness.
- a thick steel plate is used.
- the Ti content is preferably 0.008% or more, and more preferably 0.010% or more.
- the Ti content is preferably 0.025% or less, and more preferably 0.020% or less.
- Nb is an element that lowers the recrystallization temperature, and suppresses the recrystallization of austenite and contributes to the refinement of the structure during hot rolling, so 0.005% or more is added. If Nb is added excessively, the yield stress increases due to excessive precipitation strengthening and the yield ratio increases, so the content is made less than 0.035%. From the viewpoint of reducing the yield ratio, the Nb content is more preferably 0.025% or less, and further preferably 0.020% or less.
- N is an element that forms nitrides, particularly TiN, and contributes to the refinement of the structure, and contains 0.001% or more. In order to make the structure fine, it is preferable to contain 0.002% or more of N, more preferably 0.003% or more. If the amount of N becomes excessive, coarse nitrides are formed and the toughness is impaired, so the upper limit is made 0.008%.
- the upper limit of N content is preferably 0.007%, more preferably 0.006%.
- one or two of Si and Al are used as a deoxidizing element.
- Si is effective as a deoxidizer.
- Al addition is not essential.
- addition of 0.01% or more is preferable.
- Si is an element that increases the strength by solid solution strengthening, addition of 0.05% or more is more preferable, and addition of 0.10% or more is more preferable. If Si is added in an amount exceeding 0.60%, ductility, toughness, and electroweldability are impaired, so the upper limit is made 0.60%. From the viewpoint of ensuring toughness, the Si content is preferably 0.40% or less, and more preferably 0.30% or less.
- Al is effective as a deoxidizer.
- Si is added, addition is not essential.
- 0.001% or more of addition is preferable.
- 0.005% or more of Al is preferably added, and 0.01% or more of addition is more preferable.
- Al is added in excess of 0.10%, inclusions increase and ductility and toughness are impaired, so the content is limited to 0.10% or less. From the viewpoint of ensuring toughness, the Al content is preferably 0.05% or less, and more preferably 0.03% or less.
- the content of impurities P and S is limited.
- P and S are not intentionally added elements, but P and S contained in the raw materials are mixed.
- both contents are large, the following restrictions are imposed.
- P is an impurity, and the upper limit of the content is 0.02%. Since the grain boundary fracture is prevented and the toughness is improved by reducing the amount of P, the amount of P is preferably 0.015% or less, and more preferably 0.010% or less. Since it is preferable that the amount of P is small, there is no lower limit. Usually, 0.001% or more is contained from the balance between characteristics and cost.
- S is an impurity, and the upper limit of the content is 0.005%.
- the amount of S is preferably 0.003% or less, and more preferably 0.002% or less. Since a smaller amount of S is preferable, no lower limit is provided. Usually, 0.0001% or more is contained from the balance between characteristics and cost.
- Ceq is an index of hardenability and may be used as an index of strength. It calculates
- the lower limit of Ceq is preferably 0.25 or more.
- the upper limit of Ceq is preferably 0.35 or less, and more preferably 0.30 or less.
- C, Mn, Cr, Mo, V, Ni, and Cu are the content [% by mass] of each element.
- Cr, Mo, V, Ni, and Cu are elements that are selectively added in the present invention.
- Cr is calculated as 0 in the above (Equation 1).
- one or more of Ni, Cu, Cr, Mo, and V can be added to improve the hardenability of the steel and increase the strength.
- 1 type, or 2 or more types of Ca and REM can be added. Since these elements are elements that are arbitrarily added and are not essential additive elements, the lower limit of the content is not specified. In the following description, a preferable lower limit value is described. This is a preferable lower limit value for obtaining the effect of improving the hardenability and increasing the strength by adding each element. Even if the content of each element is less than the preferred lower limit, the steel is not adversely affected.
- Ni is an element that improves the hardenability of steel and contributes to the improvement of toughness.
- the Ni content is preferably 0.05% or more.
- the upper limit is made 1.0%, more preferably 0.5% or less, and even more preferably 0.3% or less.
- Cu is an element that improves the hardenability of steel and contributes to solid solution strengthening, so 0.05% or more is preferably added. If Cu is added excessively, the surface properties of the steel sheet may be impaired, so the upper limit is made 1.0% or less. From the economical viewpoint, the upper limit of the amount of Cu is more preferably 0.5%, and further preferably 0.3% or less. When adding Cu, it is preferable to add Ni simultaneously from the viewpoint of preventing deterioration of surface properties.
- Cr is an element effective for improving the strength, and it is preferable to add 0.05% or more. If Cr is added excessively, the weldability may deteriorate when the ends of the steel pipe are butted together (on-site welding), so 1.0% is made the upper limit. More preferably, it is 0.5% or less, More preferably, it is 0.2% or less.
- Mo is an element that contributes to increasing the strength of steel, and it is preferable to add 0.05% or more.
- Mo is an expensive element, and the upper limit is 0.5%.
- a more preferable upper limit of the Mo amount is 0.3% or less, and further preferably 0.1% or less.
- V is an element that generates carbides and nitrides and improves the strength of the steel by precipitation strengthening. In order to effectively increase the strength, it is preferable to add 0.01% or more. If V is added excessively, carbides and nitrides become coarse and the yield ratio may increase, so the upper limit of the V amount is 0.2%. From the viewpoint of reducing the yield ratio, the upper limit of the V amount is more preferably 0.1% or less, and even more preferably 0.05% or less.
- Ca and REM control the form of sulfide inclusions, improve the low temperature toughness, and further refine the oxide of the ERW weld to improve the toughness of the ERW weld, so one or both Is preferably added in an amount of 0.001% or more. If Ca and REM are added excessively, oxides and sulfides increase and adversely affect toughness. Therefore, the upper limit of the addition amount is set to 0.006%.
- REM is a general term for Sc, Y, La, Ce, Pr, Nd, Pm, Sm, Eu, Gd, Tb, Dy, Ho, Er, Tm, Yb, and Lu.
- the remainder of the composition of the base material of the ERW welded steel pipe according to the present invention other than those described above is iron and unavoidable impurities.
- Inevitable impurities are components contained in raw materials or mixed in during the manufacturing process, and are components not intentionally contained in steel.
- P and S must be controlled to be 0.02% or less and 0.005% or less, respectively. It is preferable to control O to be 0.006% or less.
- Sb, Sn, W, Co, and As are usually unavoidable 0.1% or less, Mg, Pb, and Bi are 0.005% or less, and B and H are 0.0005% or less. There may be contamination as an impurity, but there is no need to control in the normal range.
- Si, Al, Ni, Cu, Cr, Mo, V, Ca, and REM which are optional elements or optional elements in the steel pipe of the present invention, are mixed as inevitable impurities even if they are not intended to be contained.
- the steel pipe of the present invention is not adversely affected as long as it is below the upper limit of the content when intentionally contained.
- N may be treated as an inevitable impurity in steel, but in the electric resistance welded steel pipe of the present invention, it is necessary to control it within a certain range as described above.
- the base metal structure of the electric resistance welded steel pipe of the present invention is a martensite and the balance is a multiphase structure made of ferrite.
- the area ratio of martensite is 3% or more in order to reduce the yield ratio.
- the area ratio of martensite is preferably 5% or more, and more preferably 8% or more. Since the toughness decreases when the martensite increases, the upper limit of the martensite area ratio is set to 13%.
- the area ratio of martensite is preferably 12% or less, and more preferably 10% or less.
- the area ratio of martensite is obtained with an optical microscope after performing repeller etching. As the retained austenite increases, the martensite hardness decreases and the yield ratio increases. Therefore, in the present invention, the volume fraction of retained austenite is measured by an X-ray diffraction method, and if the volume fraction of retained austenite is 1% or less, it is determined that the metal structure is a multiphase structure composed of martensite and ferrite. It shall be.
- Martensite is preferably dispersed in ferrite with an average equivalent circle diameter of 0.5 to 1.5 ⁇ m.
- the average value of the equivalent circle diameter of martensite is less than 0.5 ⁇ m, it does not contribute to the decrease in the yield ratio.
- the average value of the equivalent circle diameter of martensite exceeds 1.5 ⁇ m, the low temperature toughness is impaired.
- the average value of the equivalent circle diameter of martensite is more preferably 0.7 to 1.1 ⁇ m.
- the maximum equivalent circle diameter is 7 ⁇ m or less, more preferably 5 ⁇ m or less, and the standard deviation is 1 ⁇ m or less, more preferably 0.8 ⁇ m or less.
- the steel slab is heated and hot-rolled, controlled cooling, wound and air-cooled to produce a hot-rolled steel sheet.
- the heating temperature of the steel slab is preferably 1150 ° C. or higher in order to dissolve elements forming carbides such as Nb in the steel. If the heating temperature is too high, the structure becomes coarse. Therefore, 1250 ° C. or lower is preferable in order to prevent coarsening of the ferrite grain size.
- Hot rolling needs to be performed in a temperature range where the steel structure is an austenite phase. This is because if the rolling is performed after the ferrite transformation has started, processed ferrite is generated and the anisotropy of the characteristics is increased. Therefore, the finishing temperature of hot rolling is preferably Ar 3 or higher at which ferrite transformation during cooling starts. If the finishing temperature is too high, the structure becomes coarse, so Ar 3 + 50 ° C. or lower is preferable.
- Ar 3 can be obtained from the thermal expansion behavior when heated and cooled using a test material having the same component as the base steel plate. Moreover, it is also possible to obtain
- C, Mn, Ni, Cu, Cr, and Mo are the content [% by mass] of each element.
- Ni, Cu, Cr, and Mo are arbitrary additive elements in the present invention. When these elements are not added intentionally, the calculation is made as 0 in the above (Formula 2).
- the amount of reduction at 950 ° C. or lower is 70% or more. Depending on the thickness of the steel slab, hot rolling may be performed at a temperature exceeding 950 ° C. However, in order to promote ferrite transformation, it is preferable to increase the amount of rolling at 950 ° C. or less to accumulate strain.
- the amount of reduction at 950 ° C. or lower is obtained as a percentage by dividing the difference between the plate thickness at 950 ° C. and the plate thickness after finish rolling by the plate thickness after finish rolling.
- accelerated cooling is performed from a temperature of 750 ° C. or higher, preferably Ar 3 or higher, in order to generate martensite. If the temperature is lowered too much after hot rolling, coarse polygonal ferrite is produced, and the strength may be lowered or the toughness may be deteriorated.
- the accelerated cooling is a two-stage cooling in which the average cooling of the previous stage up to 650 ° C. is 10 to 25 ° C./s, and the average cooling speed of the latter stage is 20 to 50 ° C./s until the accelerated cooling is stopped below 650 ° C. .
- the cooling rate of the latter stage is 1.5 times or more, preferably 2 times or more the cooling rate of the former stage.
- the above-mentioned two-stage cooling is achieved by generating ferrite in the first stage cooling and increasing the cooling rate in the second stage, thereby generating martensite without generating pearlite and without remaining austenite. This is because a multiphase structure of ferrite and martensite is obtained.
- Accelerated cooling stop temperature is set to 300 ° C. or lower, which is sufficiently lower than the Ms point, and by producing a hot-rolled steel strip by winding, hard martensite can be generated and the yield ratio can be lowered.
- the accelerated cooling stop temperature exceeds 100 ° C., the area ratio of martensite is insufficient or austenite remains excessively, and the yield ratio is not sufficiently lowered.
- the obtained hot-rolled steel strip is air-cooled, formed into a tube in the cold, and the ends are butt-welded and electro-welded to produce an electro-welded steel pipe.
- the present invention is an invention assuming a thick-walled ERW steel pipe having a small outer diameter.
- the ratio t / D of the thickness t of the base metal and the outer diameter D of the ERW steel pipe is about 2.0 to 6.0%, and is required for pipelines laid in the deep sea.
- T is 12.5 mm or more and t / D is 5.0% or more.
- a seam heat treatment may be applied in which only the ERW weld is heated and accelerated.
- ERW welding the butt portion is heated and melted, pressure is applied, and solid phase bonding is performed. Therefore, the vicinity of the ERW weld portion is plastically deformed at a high temperature and then rapidly cooled. Therefore, the ERW welded part is harder than the base metal, and the low temperature toughness and deformation performance of the ERW steel pipe can be further improved by performing seam heat treatment.
- Steel having chemical components shown in Table 1 was cast into a steel slab. These steel slabs were heated to the heating temperature shown in Table 2, hot rolling was performed at a rolling finishing temperature (FT in Table 2) of 3 or more Ar points, and accelerated cooling was performed to obtain a base steel plate.
- the accelerated cooling is a two-stage cooling in which the cooling rate is changed at 650 ° C., and the average cooling rate in the latter stage (up to 650 ° C.) is about twice the average cooling rate in the previous stage (up to 650 ° C.).
- the steel plate after accelerated cooling was wound at a winding temperature (CT) shown in Table 2 to obtain a hot-rolled steel strip.
- CT winding temperature
- the obtained hot-rolled steel strip was air-cooled, it was formed into a tubular shape in a continuous roll forming process, and the ends of the hot-rolled steel strip were butted together and subjected to electric resistance welding. Then, if necessary, the electrowelded part was heated, accelerated and cooled, and subjected to seam heat treatment.
- the amount of reduction” in Table 2 is the amount of reduction at 950 ° C. or lower in the hot rolling process, and the difference between the plate thickness at 950 ° C. and the plate thickness after finish rolling is the plate thickness after finish rolling. The percentage is obtained by dividing by. “T” indicates the thickness of the steel sheet, and “D” indicates the outer diameter of the steel pipe after pipe making.
- Ar 3 in Table 1 was determined from the content [% by mass] of C, Mn, Ni, Cu, Cr, and Mo shown in Table 1.
- Ni, Cu, Cr, and Mo are arbitrary additive elements in the present invention. As shown in the blank in Table 1, when not intentionally added, calculation was made as 0 in the following (Formula 2). .
- all of the examples of the present invention have a metal structure composed of martensite and ferrite having an appropriate area ratio, and the tensile strength of the ERW welded steel pipe is X56 or more (tensile strength of 490 MPa or more). The yield ratio is good at 90% or less.
- all of the inventive examples exhibited high Charpy absorbed energy of 190 J or more even at ⁇ 30 ° C. and good toughness.
- No. No. 21 is an example in which since the amount of C is small, the strength is lowered, the generation of martensite is insufficient, and the yield ratio is increased.
- No. No. 22 has a large amount of C.
- No. 23 is an example in which the amount of Mn is large, martensite is excessively generated, and the toughness is lowered.
- No. No. 24 is an example in which the strength is reduced because the amount of Mn is small.
- No. No. 25 is an example in which Ceq is too high, martensite is excessively generated, and toughness is lowered.
- No. No. 26 is an example in which the strength is lowered because Ceq is too low.
- No. No. 27 is an example in which the toughness is reduced because the Ti amount is small, and the bainite is generated in addition to the ferrite and the yield ratio is increased because the Nb amount is large.
- No. No. 28 is 650 ° C. or lower; martensite is not generated because the cooling speed is slow, and the yield ratio is increased.
- no. No. 29 is an example in which the accelerated cooling rate is as high as 450 ° C. and martensite is not generated and the yield ratio is increased.
- an ERW welded steel pipe having X60 to 70 grade strength that can be used for pipelines laid in the deep sea, etc., sufficient low temperature toughness, and low yield ratio. Therefore, industrial applicability is great.
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Abstract
Description
C :0.05~0.10%、
Mn:1.00~1.60%、
Ti:0.005~0.030%、
Nb:0.005%以上、0.035%未満、及び
N :0.001~0.008%
を含有し、さらに、
Si:0.01~0.60%、及び
Al:0.001~0.10%
の一方又は双方を含有し、
P :0.02%以下、
S :0.005%以下、及び
に制限され、
残部が鉄及び不可避的不純物であり、
下記(式1)で表わされるCeqが、0.23≦Ceq≦0.38を満たし、かつ、
母材の金属組織が、面積率で3~13%のマルテンサイトを含有し、残部がフェライトである
ことを特徴とする電縫溶接鋼管。
ここで、(式1)におけるC、M、Cr、Mo、V、Ni、Cuは、各元素の含有量を質量%で表した値である。
Ni:1.0%以下、
Cu:1.0%以下、
Cr:1.0%以下、
Mo:0.5%以下、
V :0.2%以下、
Ca:0.006%以下、及び
REM:0.006%以下
のうち1種又は2種以上を含有することを特徴とする前記(1)の電縫溶接鋼管。
Mn:1.00~1.50%、
Si:0.40%以下、
を満たし、さらに、
0.23≦Ceq≦0.30
を満たし、
前記母材の金属組織のマルテンサイトの円相当径の平均値が0.5~1.5μmであり、かつ、
鋼管の引張強度が520~790MPaである
ことを特徴とする前記(1)の電縫溶接鋼管。
Nb:0.005~0.020%
を満たすことを特徴とする前記(3)の電縫溶接鋼管。
Ni:0.5%以下、
Cu:0.5%以下、
Cr:0.5%以下、
Mo:0.2%以下、
V :0.1%以下、
Ca:0.006%以下、及び
REM:0.006%以下
のうち1種又は2種以上を含有することを特徴とする前記(3)又は(4)の電縫溶接鋼管。
図3(a)は、本発明の範囲内の組成を有する電縫溶接鋼管の光学顕微鏡写真であり、図3(b)はそれをレペラーエッチングした後に観察した光学顕微鏡写真である。
図2(b)、図3(b)を比較して分かるように、NbC等の析出物を利用して高強度化を図る従来の電縫溶接鋼管の場合、レペラーエッチングにより白くなった相、つまりマルテンサイトはほとんど観察されなかったが、図3(b)の本発明の場合は、マルテンサイトが観察された。
Cは、鋼の強度を高める有用な元素であり、マルテンサイトを増加させ鋼を硬質化し、降伏比の低下にも寄与するので、下限を0.05%とする。C量が0.10%を超えると現地溶接性が悪くなると共に、マルテンサイトの面積率が増加して、強度が高くなりすぎ、靭性が劣化するので、上限を0.10%とする。強度を確保する観点からは、C量を0.06%以上にすることが好ましい。強度を過剰に上昇させず、靱性を確保する観点からは、C量を0.08%以下にすることが好ましい。
Mnは、鋼の焼入れ性を高める元素であり、マルテンサイトの生成に寄与する。本発明では、強度を確保するために、1.00%以上のMnを添加する。Mnを過度に添加すると、マルテンサイトの面積率が増加し、靱性が劣化するので、上限を1.60%とする。強度を確保する観点からは、Mn量を1.10%以上にすることが好ましく、1.20%以上がより好ましい。靱性を確保する観点からは、Mn量を1.50%以下にすることが好ましく、1.40%以下がより好ましい。
Tiは、炭窒化物を形成する元素であり、組織を微細化し、靭性の向上に寄与する。本願発明は厚肉の鋼板を用いることをしており、特に、厚肉の鋼板で低温における靭性を確保するためには、0.005%以上のTiを添加することが必要である。Tiを過剰に添加するとTiNの粗大化や、TiCによる析出硬化が生じ、靭性が劣化し、降伏比が上昇するので、0.030%を上限とする。組織を微細化して靱性を確保する観点からは、Ti量を0.008%以上にすることが好ましく、0.010%以上がより好ましい。析出物に起因する降伏比の低下を抑制する観点からは、Ti量は0.025%以下が好ましく、0.020%以下がより好ましい。
Nbは、再結晶温度を低下させる元素であり、熱間圧延を行う際に、オーステナイトの再結晶を抑制して組織の微細化に寄与するので、0.005%以上を添加する。Nbを過剰に添加すると過剰な析出強化によって降伏応力が上昇し、降伏比が高くなるので、含有量は0.035%未満とする。降伏比を低下させる観点からは、Nb量を0.025%以下にすることがより好ましく、0.020%以下がさらに好ましい。
Nは、窒化物、特に、TiNを形成し、組織の微細化に寄与する元素であり、0.001%以上を含有させる。組織を微細にするためには、0.002%以上のNを含有させることが好ましく、より好ましくは含有量を0.003%以上とする。N量が過剰になると、粗大な窒化物を生じ、靭性を損なうため、上限を0.008%とする。N量の上限は0.007%が好ましく、より好ましくは0.006%とする。
Siは、脱酸剤として有効である。Alが添加されている場合には、添加は必須ではない。脱酸剤としての効果を得るためには、0.01%以上の添加が好ましい。また、Siは固溶強化によって強度を高める元素であるので、0.05%以上の添加がより好ましく、0.10%以上の添加がより好ましい。Siは、0.60%を超えて添加すると、延性や靭性、さらには、電縫溶接性を損なうので、上限を0.60%とする。靱性を確保する観点からは、Si量を0.40%以下にすることが好ましく、0.30%以下がより好ましい。
Alは、脱酸剤として有効である。Siが添加されている場合には、添加は必須ではない。脱酸剤としての効果を得るためには、0.001%以上の添加が好ましい。脱酸の効果を高めるためには、0.005%以上のAlの添加が好ましく、0.01%以上の添加がより好ましい。Alは、0.10%を超えて添加すると、介在物が増加して、延性や靭性を損なうので、0.10%以下に制限する。靱性を確保する観点からは、Al量を0.05%以下にすることが好ましく、0.03%以下がより好ましい。
Pは、不純物であり、含有量の上限を0.02%とする。P量の低減により、粒界破壊が防止され、靭性が向上することから、P量は0.015%以下が好ましく、0.010%以下がより好ましい。P量は少ない方が好ましいので、下限は設けない。特性とコストのバランスから、通常は、0.001%以上が含有される。
Sは、不純物であり、含有量の上限を0.005%とする。S量の低減により、熱間圧延によって延伸化するMnSを低減し、靭性を向上させることができることから、S量は0.003%以下が好ましく、0.002%以下がより好ましい。S量は少ない方が好ましいので、下限は設けない。特性とコストのバランスから、通常は、0.0001%以上が含有される。
炭素当量Ceqは、焼入れ性の指標であり、強度の指標としても使用されることがある。C、Mn、Cr、Mo、V、Ni、Cuの含有量[質量%]から、下記(式1)によって求める。強度を確保するためには、Ceqを0.23以上にすることが必要である。靱性を確保するためには、Ceqを0.38以下にすることが必要である。Ceqの下限は、0.25以上が好ましい。Ceqの上限は、0.35以下が好ましく、0.30以下がより好ましい。
Niは、鋼の焼入れ性を向上させる元素であり、靭性の向上にも寄与する。強度を向上させるためには、Ni量を0.05%以上にすることが好ましい。また、Niは高価な元素であるため、上限は1.0%とし、0.5%以下とすることがより好ましく、0.3%以下がさらに好ましい。
Cuは、鋼の焼入れ性を向上させる元素であり、固溶強化にも寄与するので、0.05%以上を添加することが好ましい。Cuを過度に添加すると鋼板の表面性状を損なうことがあるため、上限は1.0%以下とする。経済性の観点から、Cu量のより好ましい上限は0.5%であり、0.3%以下がさらに好ましい。Cuを添加する場合は、表面性状劣化防止の観点から、同時にNiを添加することが好ましい。
Crは、強度の向上に有効な元素であり、0.05%以上を添加することが好ましい。Crを過度に添加すると、鋼管の端部同士を突合せて溶接(現地溶接)する際に、溶接性が劣化することがあるので、1.0%を上限とする。より好ましくは0.5%以下であり、さらに好ましくは0.2%以下である。
Moは、鋼の高強度化に寄与する元素であり、0.05%以上を添加することが好ましい。ただし、Moは高価な元素であり、0.5%を上限とする。より好ましいMo量の上限は0.3%以下であり、さらに好ましくは0.1%以下とする。
Vは、炭化物、窒化物を生成し、析出強化によって鋼の強度を向上させる元素であり、強度を効果的に上昇させるために、0.01%以上を添加することが好ましい。Vを過剰に添加すると、炭化物及び窒化物が粗大化し、降伏比が上昇することがあるので、V量の上限は0.2%とする。降伏比を低下させる観点からは、V量の上限を0.1%以下にすることがより好ましく、さらに好ましくは0.05%以下とする。
Ca、REMは、硫化物系介在物の形態を制御し、低温靭性を向上させ、さらに、電縫溶接部の酸化物を微細化して電縫溶接部の靭性を向上させるので、一方、又は双方を0.001%以上添加することが好ましい。Ca、REMを過剰に添加すると、酸化物・硫化物が大きくなり靭性に悪影響を及ぼすので、添加量の上限は0.006%とする。ここでREMとは、Sc、Y、La、Ce、Pr、Nd、Pm、Sm、Eu、Gd、Tb、Dy、Ho、Er、Tm、Yb、Luの総称である。
本発明の電縫溶接鋼管の母材の金属組織はマルテンサイトと、残部はフェライトからなる複相組織とする。マルテンサイトの面積率は、降伏比を低下させるために、3%以上とする。マルテンサイトの面積率は5%以上が好ましく、8%以上がより好ましい。マルテンサイトが増加すると靱性が低下するので、マルテンサイトの面積率の上限は13%とする。マルテンサイトの面積率は12%以下が好ましく、10%以下がより好ましい。
まず、本発明の電縫溶接鋼管の素材である熱延鋼板の製造条件について説明する。
-15Cr-80Mo … (式2)
-15Cr-80Mo ・・・ (式2)
Claims (5)
- 母材の成分組成が、質量%で、
C :0.05~0.10%、
Mn:1.00~1.60%、
Ti:0.005~0.030%、
Nb:0.005%以上、0.035%未満、及び
N :0.001~0.008%
を含有し、さらに、
Si:0.01~0.60%、及び
Al:0.001~0.10%
の一方又は双方を含有し、
P :0.02%以下、
S :0.005%以下、及び
に制限され、
残部が鉄及び不可避的不純物であり、
下記(式1)で表わされるCeqが、0.23≦Ceq≦0.38を満たし、かつ、
母材の金属組織が、面積率で3~13%のマルテンサイトを含有し、残部がフェライトである
ことを特徴とする電縫溶接鋼管。
Ceq=C+Mn/6+(Cr+Mo+V)/5+(Ni+Cu)/15…(式1)
ここで、(式1)におけるC、M、Cr、Mo、V、Ni、Cuは、各元素の含有量を質量%で表した値である。 - 前記母材の成分組成が、さらに、質量%で、
Ni:1.0%以下、
Cu:1.0%以下、
Cr:1.0%以下、
Mo:0.5%以下、
V :0.2%以下、
Ca:0.006%以下、及び
REM:0.006%以下
のうち1種又は2種以上を含有することを特徴とする請求項1に記載の電縫溶接鋼管。 - 前記母材の成分組成が、
Mn:1.00~1.50%、
Si:0.40%以下、
を満たし、さらに、
0.23≦Ceq≦0.30
を満たし、
前記母材の金属組織のマルテンサイトの円相当径の平均値が0.5~1.5μmであり、かつ、
鋼管の引張強度が490~760MPaである
ことを特徴とする請求項1に記載の電縫溶接鋼管。 - 前記母材の成分組成が、
Nb:0.005~0.020%
を満たすことを特徴とする請求項3に記載の電縫溶接鋼管。 - 前記母材の成分組成が、さらに、質量%で、
Ni:0.5%以下、
Cu:0.5%以下、
Cr:0.5%以下、
Mo:0.2%以下、
V :0.1%以下、
Ca:0.006%以下、及び
REM:0.006%以下
のうち1種又は2種以上を含有することを特徴とする請求項3又は4に記載の電縫溶接鋼管。
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EP13840703.6A EP2902519A4 (en) | 2012-09-27 | 2013-09-27 | RESISTANT WELDED STEEL TUBE |
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CN113549846A (zh) * | 2021-07-13 | 2021-10-26 | 鞍钢股份有限公司 | 一种低温性能优异的550MPa级海工钢及其制造方法 |
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US20220373108A1 (en) * | 2019-10-31 | 2022-11-24 | Jfe Steel Corporation | Electric resistance welded steel pipe, method for producing the same, line pipe, and building structure |
KR102503447B1 (ko) * | 2020-12-21 | 2023-02-28 | 현대제철 주식회사 | 용접성이 우수한 라인파이프용 강재 및 그 제조방법 |
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- 2013-09-27 CA CA2881372A patent/CA2881372C/en not_active Expired - Fee Related
- 2013-09-27 CN CN201380030721.0A patent/CN104350168B/zh not_active Expired - Fee Related
- 2013-09-27 JP JP2014500584A patent/JP5516834B1/ja active Active
- 2013-09-27 KR KR1020147032630A patent/KR101605152B1/ko active IP Right Grant
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Also Published As
Publication number | Publication date |
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US9726305B2 (en) | 2017-08-08 |
KR20150002871A (ko) | 2015-01-07 |
JPWO2014051119A1 (ja) | 2016-08-25 |
CA2881372A1 (en) | 2014-04-03 |
CN104350168A (zh) | 2015-02-11 |
EP2902519A4 (en) | 2016-06-01 |
CA2881372C (en) | 2017-11-21 |
US20150219249A1 (en) | 2015-08-06 |
CN104350168B (zh) | 2016-08-24 |
EP2902519A1 (en) | 2015-08-05 |
JP5516834B1 (ja) | 2014-06-11 |
KR101605152B1 (ko) | 2016-03-21 |
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