WO2016079908A1 - 油井用高強度継目無鋼管およびその製造方法 - Google Patents
油井用高強度継目無鋼管およびその製造方法 Download PDFInfo
- Publication number
- WO2016079908A1 WO2016079908A1 PCT/JP2015/004182 JP2015004182W WO2016079908A1 WO 2016079908 A1 WO2016079908 A1 WO 2016079908A1 JP 2015004182 W JP2015004182 W JP 2015004182W WO 2016079908 A1 WO2016079908 A1 WO 2016079908A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- less
- steel pipe
- inclusions
- seamless steel
- temperature
- Prior art date
Links
Classifications
-
- 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
- C21D9/08—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for tubular bodies or pipes
- C21D9/085—Cooling or quenching
-
- 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
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
-
- 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
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/02—Hardening by precipitation
-
- 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
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/10—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of tubular bodies
-
- 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
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/10—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of tubular bodies
- C21D8/105—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of tubular bodies of ferrous alloys
-
- 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
- C21D9/08—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for tubular bodies or pipes
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
-
- 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
- C22C38/20—Ferrous alloys, e.g. steel alloys containing chromium with copper
-
- 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
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
-
- 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
- C22C38/24—Ferrous alloys, e.g. steel alloys containing chromium with vanadium
-
- 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
-
- 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
-
- 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
- C22C38/32—Ferrous alloys, e.g. steel alloys containing chromium with boron
-
- 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
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
-
- 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
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/42—Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
-
- 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
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/44—Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
-
- 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
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/46—Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
-
- 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
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/48—Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
-
- 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
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/50—Ferrous alloys, e.g. steel alloys containing chromium with nickel with titanium or zirconium
-
- 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
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/54—Ferrous alloys, e.g. steel alloys containing chromium with nickel with boron
-
- 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
- C21D2211/001—Austenite
-
- 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
- C21D2211/004—Dispersions; Precipitations
-
- 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
Definitions
- the present invention relates to a high-strength seamless steel pipe suitable for use in oil well pipes and line pipes, and more particularly to improvement of resistance to sulfide stress corrosion cracking (SSC resistance) in a wet hydrogen sulfide environment (sour environment). .
- SSC resistance sulfide stress corrosion cracking
- Patent Document 1 In response to such a demand, for example, in Patent Document 1, C: 0.2 to 0.35%, Cr: 0.2 to 0.7%, Mo: 0.1 to 0.5%, V: 0.1 to 0.3%, and C, There has been proposed a method for producing oil well steel in which Cr, Mo and V are adjusted and a low alloy steel is quenched at the Ac 3 transformation point or higher and then tempered at 650 ° C. or higher and the Ac 1 transformation point or lower. According to the technique described in Patent Document 1, the total amount of precipitated carbide can be adjusted to 2 to 5% by weight, and the proportion of MC type carbide in the total amount of carbide can be adjusted to 8 to 40% by weight. It is said that oil well steel having excellent resistance to sulfide stress corrosion cracking can be obtained.
- Patent Document 2 discloses a low alloy containing, by mass, C: 0.15 to 0.3%, Cr: 0.2 to 1.5%, Mo: 0.1 to 1%, V: 0.05 to 0.3%, and Nb: 0.003 to 0.1%.
- the hot working is finished at 1000 ° C or higher and subsequently quenched from 900 ° C or higher, then tempered at 550 ° C or higher and below the Ac 1 transformation point, and further 850-1000 ° C.
- the total amount of precipitated carbide is 1.5 to 4% by mass, and the proportion of MC type carbide in the total amount of carbide is 5 to 45% by mass.
- M 23 C 6 type carbide This ratio can be adjusted to 200 / t (t: wall thickness (mm)) mass% or less, and it is said that the oil well steel is excellent in toughness and resistance to sulfide stress corrosion cracking.
- Patent Document 3 describes, in mass%, C: 0.15-0.30%, Si: 0.05-1.0%, Mn: 0.10-1.0%, Cr: 0.1-1.5%, Mo: 0.1-1.0%, Al: 0.003. -0.08%, N: 0.008% or less, B: 0.0005-0.010%, Ca + O: 0.008% or less, Ti: 0.005-0.05%, Nb: 0.05% or less, Zr: 0.05% or less, V: 0.30% or less contain one or two or more of, is 80 ⁇ m or less than the maximum length of the non-metallic inclusions continuously by cross-section observation, the number of more than the particle size 20 ⁇ m of non-metallic inclusions by the cross section observation is 10/100 mm 2
- the following steel materials for oil wells have been proposed. Thereby, it is said that a low alloy steel material for oil wells having high strength required for oil wells and excellent SSC resistance commensurate with the strength is obtained.
- Patent Document 4 in mass%, C: 0.20 to 0.35%, Si: 0.05 to 0.5%, Mn: 0.05 to 0.6%, P %: 0.025% or less, S: 0.01% or less, Al: 0.005 to 0.100 %, Mo: 0.8 to 3.0%, V: 0.05 to 0.25%, B: 0.0001 to 0.005%, N: 0.01% or less, O: 0.01% or less and sulfide stress corrosion resistance satisfying 12V + 1-Mo ⁇ 0 Low alloy oil well pipe steels with excellent cracking properties have been proposed.
- Cr 0.6% or less may be contained so as to satisfy Mo ⁇ (Cr + Mn) ⁇ 0, and Nb: 0.1% or less, Ti : 0.1% or less, Zr: One or more of 0.1% or less may be contained, and Ca: 0.01% or less may be contained.
- An object of the present invention is to solve the problems of the prior art and to provide a high-strength seamless steel pipe for oil wells excellent in sulfide stress corrosion cracking resistance and a method for producing the same.
- “high strength” here refers to the case where the yield strength YS is 125 ksi (862 MPa) or more.
- “excellent in resistance to sulfide stress corrosion cracking” as used herein means 5.0 mass by which 10 kPa of hydrogen sulfide is saturated and the pH is adjusted to 3.5 in accordance with the test method specified in NACE TM0177 Method A. A constant load test is performed in an acetic acid-sodium acetate aqueous solution (liquid temperature: 24 ° C) containing a 1% sodium chloride aqueous solution, and cracks do not occur over 720h with a stress of 85% of the yield strength of the material under test. It shall be a case.
- Nitride inclusions with a particle size of 4 ⁇ m or more and oxide inclusions with a particle size of 4 ⁇ m or more are the starting points of sulfide stress corrosion cracking (SSC). The larger the size, the more likely SSC is generated. I found out.
- Nitride inclusions having a particle size of less than 4 ⁇ m do not become the starting point of SSC even if they are present alone, but if they become a large number, they will adversely affect SSC resistance, and less than 4 ⁇ m It has been found that a large number of oxide inclusions adversely affects SSC resistance.
- the inventors reduced the number of nitride inclusions and oxide inclusions to an appropriate number or less depending on the size. I came up with the need to adjust.
- the amount of N and amount of O in the production of steel pipe materials particularly during the melting and casting of molten steel. It is important to control so that the value falls within the desired range. Furthermore, it is important to manage manufacturing conditions in the steel refining process and the continuous casting process.
- the present invention has been completed based on such findings and further studies. That is, the gist of the present invention is as follows. (1) By mass%, C: 0.20 to 0.50%, Si: 0.05 to 0.40%, Mn: 0.3 to 0.9%, P: 0.015% or less, S: 0.005% or less, Al: 0.005 to 0.1%, N: 0.006 % Or less, Cr: 0.6% to 1.7%, Mo: 1.0% to 3.0%, V: 0.02 to 0.3%, Nb: 0.001 to 0.02%, B: 0.0003 to 0.0030%, O (oxygen): 0.0030% or less , Ti: 0.003 to 0.025%, Ti and N are contained so as to satisfy Ti / N: 2.0 to 5.0, and the balance is composed of Fe and inevitable impurities, and the volume ratio of tempered martensite 95% or more, prior austenite grains with a grain size number of 8.5 or more, and in a cross section perpendicular to the rolling direction, 100 or less nitride
- a method for producing a seamless steel pipe for oil wells in which a steel pipe material is heated and subjected to hot working to obtain a seamless steel pipe having a predetermined shape, and the oil well use according to any one of (1) to (3)
- a method for producing a high-strength seamless steel pipe wherein the heating temperature is set to a temperature in the range of 1050 to 1350 ° C., and after the hot working, the surface temperature of the seamless steel pipe is 200 ° C. at a cooling rate higher than air cooling. Cool to the following temperature, and after the cooling, reheat to a temperature in the range of Ac 3 transformation point to 1000 ° C., quenching treatment to quench at a surface temperature of 200 ° C.
- a method for producing a high-strength seamless steel pipe for oil wells which is subjected to a tempering treatment in which a temperature in the range of 600 to 740 ° C. is applied after the quenching treatment.
- a high strength seamless steel pipe for oil wells having a high yield strength YS: 125 ksi (862 MPa) or more and excellent sulfide stress corrosion cracking resistance can be easily and inexpensively manufactured. There are remarkable effects in the industry.
- by containing an appropriate amount of an appropriate alloy element and suppressing the formation of nitride inclusions and oxide inclusions desired high strength for oil wells and excellent SSC resistance can be obtained.
- the high-strength seamless steel pipe to hold can be manufactured stably.
- C 0.20 to 0.50% C dissolves and contributes to increasing the strength of the steel, improves the hardenability of the steel, and contributes to the formation of a structure whose main phase is the martensite phase during quenching. In order to acquire such an effect, C needs to contain 0.20% or more. On the other hand, if the content of C exceeds 0.50%, cracking occurs during quenching, and the productivity is significantly reduced. For this reason, C is limited to the range of 0.20 to 0.50%. Preferably, C is 0.20 to 0.35%. More preferably, C is 0.22 to 0.32%.
- Si 0.05 to 0.40%
- Si is an element that acts as a deoxidizer, has a function of increasing the strength of the steel by solid solution in the steel, and further suppressing softening during tempering. In order to acquire such an effect, it is necessary to contain Si 0.05% or more.
- a large amount of Si exceeding 0.40% promotes the formation of a ferrite phase that is a softening phase, inhibits the desired high strength, and further promotes the formation of coarse oxide inclusions, Reduces SSC resistance and toughness.
- Si is an element that segregates and locally hardens the steel, and if a large amount is contained, a local hardened region is formed and the SSC resistance is adversely affected. Therefore, in the present invention, Si is limited to the range of 0.05 to 0.40%.
- Si is 0.05 to 0.30%. More preferably, Si is 0.20 to 0.30%.
- Mn 0.3-0.9%
- Mn is an element that improves the hardenability of steel and contributes to an increase in steel strength. In order to acquire such an effect, Mn needs to contain 0.3% or more.
- Mn is an element that segregates and locally hardens the steel, and the inclusion of a large amount of Mn has an adverse effect of forming a local hardening region and lowering the SSC resistance. Therefore, in the present invention, Mn is limited to a range of 0.3 to 0.9%. Preferably, Mn is 0.4 to 0.8%. More preferably, Mn is 0.5 to 0.8%.
- P 0.015% or less
- P is an element that not only segregates at grain boundaries to cause grain boundary embrittlement but also segregates and locally hardens steel.
- P is an inevitable impurity as much as possible. It is preferable to reduce it, but up to 0.015% is acceptable. For this reason, P was limited to 0.015% or less.
- P is 0.012% or less.
- S 0.005% or less S is an unavoidable impurity, most of which is present as sulfide inclusions in steel, and lowers ductility, toughness and SSC resistance. Up to 0.005% is acceptable. For this reason, S was limited to 0.005% or less. Preferably, S is 0.003% or less.
- Al acts as a deoxidizer and combines with N to form AlN, contributing to the refinement of austenite grains during heating.
- Al fixes N and prevents solute B from binding to N, thereby suppressing the reduction of the effect of improving the hardenability of B.
- Al needs to contain 0.005% or more.
- the content of Al exceeding 0.1% causes an increase in oxide inclusions, lowers the cleanliness of the steel, and leads to a decrease in ductility, toughness and SSC resistance.
- Al is limited to the range of 0.005 to 0.1%.
- Al is 0.01 to 0.08%. More preferably, Al is 0.02 to 0.05%.
- N 0.006% or less N exists in steel as an unavoidable impurity, but forms AlN by combining with Al. If Ti is contained, TiN is formed to refine crystal grains and toughness. It has the effect
- Cr 0.6% to 1.7% or less
- Cr is an element that increases the strength of steel through the improvement of hardenability and improves the corrosion resistance.
- Cr is an element that combines with C during tempering to form carbides such as M 3 C, M 7 C 3 , and M 23 C 6 (M is a metal element) and improves temper softening resistance.
- M is a metal element
- M 3 C type carbide has a strong effect of improving the temper softening resistance.
- the Cr content needs to exceed 0.6%.
- the Cr content exceeds 1.7%, a large amount of M 7 C 3 and M 23 C 6 is formed, which acts as a hydrogen trap site and lowers the SSC resistance.
- Cr was limited to a range of 0.6% to 1.7%.
- Cr is 0.8 to 1.5%. More preferably, Cr is 0.8 to 1.3%.
- Mo More than 1.0% and less than 3.0% Mo is an element that forms carbides and contributes to strengthening steel by precipitation strengthening, and is effective in securing desired high strength after reducing dislocation density by tempering. Contribute to. SSC resistance is improved by reducing the dislocation density. Mo dissolves in the steel and segregates at the prior austenite grain boundaries, contributing to the improvement of SSC resistance. Furthermore, Mo has the effect of densifying the corrosion products and further suppressing the generation and growth of pits that are the starting points of cracks. In order to obtain such an effect, the Mo content needs to exceed 1.0%.
- Mo exceed 3.0% promotes the formation of acicular M 2 C precipitates and, in some cases, the Laves phase (Fe 2 Mo), and decreases the SSC resistance.
- Mo was limited to the range of more than 1.0% and less than 3.0%.
- the Mo content is preferably more than 1.1% and less than 3.0%, more preferably more than 1.2% and less than 2.8%, and still more preferably 1.45 to 2.5%. More preferably, Mo is 1.45 to 1.80%.
- V 0.02 to 0.3%
- V is an element that forms carbides and carbonitrides and contributes to the strengthening of steel. In order to acquire such an effect, V needs to contain 0.02% or more. On the other hand, even if it contains V exceeding 0.3%, the effect is saturated and an effect commensurate with the content cannot be expected, which is economically disadvantageous. For this reason, V is limited to the range of 0.02 to 0.3%. In addition, Preferably it is 0.03 to 0.20%, More preferably, V is 0.15% or less.
- Nb 0.001 to 0.02%
- Nb forms carbides and / or carbonitrides, contributes to increasing the strength of the steel by precipitation strengthening, and also contributes to refinement of austenite grains. In order to acquire such an effect, Nb needs to contain 0.001% or more.
- Nb precipitates tend to be a propagation path of SSC (sulfide stress corrosion cracking), and the presence of a large amount of Nb precipitates based on a large amount of Nb content exceeding 0.02% is particularly high strength with yield strength of 125 ksi or more. In steel, this leads to a significant decrease in SSC resistance.
- Nb is limited to 0.001 to 0.02% from the viewpoint of achieving both desired high strength and excellent SSC resistance.
- Nb is 0.001% or more and less than 0.01%.
- B 0.0003 to 0.0030% B segregates at the austenite grain boundaries and suppresses the ferrite transformation from the grain boundaries, thereby having the effect of enhancing the hardenability of the steel even when contained in a small amount. In order to acquire such an effect, B needs to contain 0.0003% or more. On the other hand, when B is contained in excess of 0.0030%, it precipitates as carbonitride and the like, the hardenability is lowered, and thus the toughness is lowered. For this reason, B is limited to the range of 0.0003 to 0.0030%. Preferably, B is 0.0007 to 0.0025%.
- O (oxygen) 0.0030% or less
- O (oxygen) exists as an oxide inclusion in steel as an inevitable impurity. Since these inclusions become the starting point of SSC generation and reduce SSC resistance, in the present invention, it is preferable to reduce O (oxygen) as much as possible. However, excessive reduction leads to higher refining costs, so up to 0.0030% is acceptable. For this reason, O (oxygen) was limited to 0.0030% or less. In addition, Preferably, O is 0.0020% or less.
- Ti 0.003-0.025%
- Ti combines with N during solidification of molten steel and precipitates as fine TiN, which contributes to the refinement of austenite grains by its pinning effect.
- Ti needs to contain 0.003% or more.
- TiN becomes coarse and the above-described pinning effect cannot be exhibited, but the toughness is reduced.
- the coarser TiN causes the SSC resistance to decrease. For these reasons, Ti is limited to the range of 0.003 to 0.025%.
- Ti / N 2.0-5.0
- Ti / N is less than 2.0, the fixation of N is insufficient, BN is formed, and the effect of improving hardenability by B decreases.
- Ti / N is larger than 5.0, the tendency of TiN to become coarse becomes remarkable, and toughness and SSC resistance are lowered. For this reason, Ti / N was limited to the range of 2.0 to 5.0.
- Ti / N is 2.5 to 4.5.
- the above-mentioned components are basic components.
- one or two elements selected from Cu: 1.0% or less, Ni: 1.0% or less, and W: 3.0% or less are further selected as the selective elements. More than species, and / or Ca: 0.0005-0.005%.
- Cu is an element that contributes to increasing the strength of steel and has the effect of improving toughness and corrosion resistance. In particular, it is an extremely effective element for improving SSC resistance in severe corrosive environments.
- Cu When Cu is contained, a dense corrosion product is formed and the corrosion resistance is improved, and further, the generation and growth of pits as the starting point of cracking are suppressed.
- it is desirable to contain Cu 0.03% or more.
- Cu even if Cu is contained in an amount exceeding 1.0%, the effect is saturated, and an effect commensurate with the content cannot be expected, which is disadvantageous for economic efficiency. For this reason, when it contains Cu, it is preferable to limit Cu to 1.0% or less.
- Ni is an element that contributes to increasing the strength of steel and further improves toughness and corrosion resistance. In order to acquire such an effect, it is desirable to contain Ni 0.03% or more. On the other hand, even if Ni is contained in an amount exceeding 1.0%, the effect is saturated, and an effect commensurate with the content cannot be expected, which is disadvantageous for economic efficiency. For this reason, when it contains Ni, it is preferable to limit Ni to 1.0% or less.
- W is an element that forms carbides and contributes to increasing the strength of the steel by precipitation strengthening, and also dissolves and segregates at the prior austenite grain boundaries to contribute to the improvement of SSC resistance.
- W is preferably contained in an amount of 0.03% or more.
- W it is preferable to limit W to 3.0% or less.
- Ca 0.0005 to 0.005%
- Ca is an element that combines with S to form CaS and effectively acts to control the morphology of sulfide inclusions, and improves toughness and SSC resistance through the morphology control of sulfide inclusions. Contribute. In order to acquire such an effect, Ca needs to contain at least 0.0005%. On the other hand, even if Ca is contained in excess of 0.005%, the effect is saturated and an effect commensurate with the content cannot be expected, which is disadvantageous in terms of economy. For this reason, when Ca is contained, Ca is preferably limited to a range of 0.0005 to 0.005%.
- the balance other than the above components is composed of Fe and inevitable impurities.
- unavoidable impurities Mg: 0.0008% or less, Co: 0.05% or less are acceptable.
- the high-strength seamless steel pipe of the present invention has the above-described composition, and further has a volume ratio of 95% or more with tempered martensite as the main phase, the prior austenite grains have a particle size number of 8.5 or more, and in the rolling direction.
- the number of nitride inclusions with a particle size of 4 ⁇ m or more is 100 or less per 100 mm 2
- the particle size is less than 1000 nitride inclusions with a size of less than 4 ⁇ m per 100 mm 2
- the particle size is 4 ⁇ m or more -based inclusions 100 mm 2 per 40 or less
- particle size: oxide inclusions of less than 4 ⁇ m has a tissue is 100 mm 2 400 per below.
- Tempered martensite phase 95% or more
- the martensite phase is used to secure the high strength of YS: 125 ksi class or higher and to maintain the ductility and toughness required for the structure.
- the tempered martensite phase is the main phase.
- the term “main phase” as used herein refers to a case where the phase is a single phase having a volume ratio of 100%, or the phase includes 95% or less of a volume ratio that does not affect the characteristics of the second phase. The case where it is more than%.
- examples of the second phase include a bainite phase, a retained austenite phase, pearlite, or a mixed phase thereof.
- the above structure of the high-strength seamless steel pipe of the present invention can be adjusted by appropriately selecting the heating temperature at the time of quenching according to the steel components and the cooling rate at the time of cooling.
- Particle size number of prior austenite grains 8.5 or more If the particle size number of prior austenite grains is less than 8.5, the substructure of the martensite phase produced becomes coarse and SSC resistance decreases. For this reason, the particle size number of the prior austenite grains is limited to 8.5 or more. As the particle number, a value measured in accordance with JIS G 0551 is used.
- the particle size number of the prior austenite grains can be adjusted by changing the heating rate, heating temperature and holding temperature in the quenching process, and the number of times of quenching process.
- the number of nitride inclusions and oxide inclusions is adjusted within an appropriate range according to the size in order to improve SSC resistance.
- the nitride inclusions and oxide inclusions are identified by automatic detection using a scanning electron microscope.
- the nitride inclusions are mainly composed of Ti and Nb, and oxide inclusions. Is composed mainly of Al, Ca, and Mg.
- the number of inclusions is a value measured in a cross section perpendicular to the rolling direction of the steel pipe (cross section perpendicular to the pipe axis direction: C cross section).
- the particle size of each inclusion is used as the size of the inclusion.
- the particle size of the inclusions was obtained by calculating the equivalent circle diameter by obtaining the area of the inclusion particles and calculating the equivalent particle diameter.
- Nitride inclusions with a grain size of 4 ⁇ m or more 100 or less per 100 mm 2
- Nitride inclusions are the origin of SSC in high-strength steel pipes with a yield strength of 125 ksi or more, and the size is as large as 4 ⁇ m or more. The worse, the worse it is. Therefore, it is desirable to reduce the number of nitride inclusions of 4 ⁇ m or more as much as possible, but if the number is 100 or less per 100 mm 2 , the adverse effect on SSC resistance can be tolerated. Therefore, the number of nitride inclusions having a particle size of 4 ⁇ m or more is limited to 100 or less per 100 mm 2 . The number is preferably 84 or less.
- Nitride inclusions with a particle size of less than 4 ⁇ m 1000 or less per 100 mm 2
- Fine nitride inclusions with a particle size of less than 4 ⁇ m are not the origin of SSC even if they exist alone, but yield strength YS:
- the number of high-strength steel pipes of 125 ksi class or higher increases, and if it exceeds 1000 per 100 mm 2 , the adverse effect on SSC resistance becomes unacceptable. For this reason, the number of nitride inclusions having a particle size of less than 4 ⁇ m is limited to 1000 or less per 100 mm 2 .
- the number is preferably 900 or less.
- Oxide inclusions have a yield strength of YS: 125 ksi class or higher. The larger it is, the greater the adverse effect. Therefore, it is desirable to reduce the number of oxide inclusions having a particle size of 4 ⁇ m or more as much as possible, but if the number is 40 or less per 100 mm 2 , an adverse effect on SSC resistance can be tolerated. For this reason, the number of oxide inclusions having a particle size of 4 ⁇ m or more is limited to 40 or less per 100 mm 2 . The number is preferably 35 or less.
- Oxide inclusions with a grain size of less than 4 ⁇ m 400 or less per 100 mm 2
- Oxide inclusions are the origin of SSC even if the grain size is less than 4 ⁇ m for high strength steels with yield strength of 125 ksi or higher.
- the adverse effect on SSC resistance increases. Therefore, it is desirable to reduce the oxide inclusions having a particle diameter of less than 4 ⁇ m as much as possible, but it is acceptable if the number is 400 or less per 100 mm 2 .
- the number of oxide inclusions having a particle size of less than 4 ⁇ m was limited to 400 or less per 100 mm 2 .
- Preferably it is 365 or less.
- the ladle from the ladle to the tundish is reduced so that the number of nitride inclusions and oxide inclusions is less than the number per unit area described above.
- sealing with an inert gas is performed, and electromagnetic stirring is performed in the mold to achieve floating separation of inclusions.
- the steel pipe material having the above composition is heated and hot-worked to obtain a seamless steel pipe having a predetermined shape.
- the steel pipe material used in the present invention is prepared by melting molten steel having the above composition by a conventional melting method such as a converter, and by a conventional casting method such as a continuous casting method. It is preferable to do.
- the slab may be further hot-rolled to obtain a round steel piece having a predetermined shape, or a round steel piece that has undergone ingot-bundling rolling.
- the number of nitride inclusions and oxide inclusions is reduced so as to be equal to or less than the above number per unit area. To do. For this reason, it is necessary to reduce the steel pipe material (slab or steel slab) as much as possible within the ranges of N (nitrogen): 0.006% or less and O (oxygen): 0.0030% or less.
- the heat stirring and refining treatment has a treatment time of 30 min or longer and the RH vacuum degassing treatment has a treatment time of 20 min or longer.
- the ladle from the ladle to the tundish is reduced so that the number of nitride inclusions and oxide inclusions is less than the number per unit area described above.
- the slab (steel pipe material) having the above composition is heated to a heating temperature of 1050 to 1350 ° C. and hot-worked to obtain a seamless steel pipe having a predetermined size.
- Heating temperature 1050-1350 ° C
- the heating temperature is less than 1050 ° C.
- the dissolution of carbides in the steel pipe material becomes insufficient.
- crystal grains become coarse, precipitates such as TiN precipitated during solidification become coarse, and cementite becomes coarse, so that the steel pipe toughness decreases.
- heating to a high temperature exceeding 1350 ° C. is not preferable from the viewpoint of energy saving because a thick scale layer is formed on the surface of the steel pipe material, causing surface flaws and the like during rolling and increasing energy loss.
- the heating temperature was limited to a temperature in the range of 1050 to 1350 ° C.
- the temperature is preferably 1100 to 1300 ° C.
- the heated steel pipe material is then subjected to hot working (pipemaking) using a Mannesmann-plug mill type or Mannesmann-Mandrel type hot rolling mill to obtain a seamless steel pipe having a predetermined dimension.
- a Mannesmann-plug mill type or Mannesmann-Mandrel type hot rolling mill to obtain a seamless steel pipe having a predetermined dimension.
- it is good also as a seamless steel pipe by the hot extrusion by a press system.
- the obtained seamless steel pipe is subjected to a cooling process of cooling at a cooling rate of air cooling or higher until the surface temperature becomes 200 ° C. or lower after the hot working is finished.
- Cooling after completion of hot working Cooling rate: Air cooling or higher, Cooling stop temperature: 200 ° C. or lower
- Cooling rate Air cooling or higher
- Cooling stop temperature 200 ° C. or lower
- the “cooling rate over air cooling” refers to 0.1 ° C./s or more.
- ⁇ Temperature treatment is performed after cooling at a cooling rate higher than air cooling.
- the tempering process is a process of heating to a temperature in the range of 600 to 740 ° C.
- Tempering temperature 600-740 °C
- the tempering treatment is performed for the purpose of reducing dislocation density and improving toughness and SSC resistance. If the tempering temperature is less than 600 ° C., the reduction of dislocations is insufficient, so that excellent SSC resistance cannot be ensured. On the other hand, when the temperature exceeds 740 ° C., the tissue is remarkably softened and the desired high strength cannot be ensured. For this reason, the tempering temperature was limited to the range of 600 to 740 ° C. The temperature is preferably 660 to 710 ° C.
- Reheating temperature for quenching treatment Ac 3 transformation point or more and 1000 ° C or less If the reheating temperature is less than the Ac 3 transformation point, the austenite single phase region is not heated, so a structure with the martensite phase as the main phase is obtained. Absent. On the other hand, when the temperature exceeds 1000 ° C., in addition to coarsening of crystal grains and lowering toughness, there are adverse effects such as thickening of the surface oxide scale, easy peeling and causing wrinkling on the surface of the steel sheet. Furthermore, the load on the heat treatment furnace becomes excessive, which causes a problem from the viewpoint of energy saving. For these reasons and from the viewpoint of energy saving, the reheating temperature for quenching is limited to the Ac 3 transformation point or higher and 1000 ° C. or lower. In addition, Preferably it is 950 degrees C or less.
- quenching treatment is performed.
- the quenching cooling is preferably performed by water cooling at an average cooling rate of 2 ° C./s or more to a temperature of 400 ° C. or less at the center position of the plate thickness, and the surface temperature is It is preferable to cool to 200 ° C. or lower, preferably to a temperature of 100 ° C. or lower.
- the quenching process may be repeated twice or more.
- the hot metal discharged from the blast furnace was desulfurized and dephosphorized in the hot metal pretreatment, decarburized and dephosphorized in the converter, and as shown in Table 2, the heat treatment and refining treatment (LF ) And RH vacuum degassing treatment with a reflux rate of 120 ton / min and a treatment time of 10 to 40 min to obtain molten steel having the composition shown in Table 1, and a slab (round slab: 190 mm ⁇ ) by a continuous casting method. .
- tundish Ar gas shielding was performed, and for other than N steel and R steel, electromagnetic stirring was performed in the mold.
- the obtained slab was placed in a heating furnace as a steel pipe material, heated to the heating temperature shown in Table 2, and held (holding time: 2 h).
- the heated steel pipe material was hot-worked using a Mannesmann-plug mill type hot rolling mill to obtain a seamless steel pipe (outer diameter 100 to 200 mm ⁇ ⁇ thickness 12 to 30 mm).
- it air-cooled and the quenching tempering process was performed on the conditions shown in Table 2. In some cases, after hot working, it was cooled with water, and then tempered or quenched and tempered.
- a test piece was collected from the obtained seamless steel pipe and subjected to a structure observation, a tensile test, and a sulfide stress corrosion cracking test.
- the test method was as follows.
- (1) Microstructure observation A specimen for microstructural observation was taken from the inner surface side 1 / 4t position (t: pipe thickness) of the obtained seamless steel pipe, and the cross section (C cross section) perpendicular to the longitudinal direction of the pipe was polished.
- Corrosion Nital (nitric acid-ethanol mixed solution) corrosion
- the prior austenite ( ⁇ ) particle size was measured using a structure observation specimen.
- the cross section (C cross section) perpendicular to the longitudinal direction of the tube of the tissue observation specimen is polished and corroded (picral liquid (picral (picric acid-ethanol mixed liquid)) to reveal the former ⁇ grain boundary, and an optical microscope ( (Magnification: 1000 times) and field of view: Imaged at 3 or more locations.
- the particle size number of the old ⁇ grains was obtained using a cutting method in accordance with the provisions of JIS G0551. It was.
- the number of particles identified as inclusions was obtained, the area of each particle was obtained, and the equivalent circle diameter was calculated to obtain the particle size of the inclusions. Then, the number density (inclusions / 100 mm 2 ) of inclusions having a particle size of 4 ⁇ m or more and inclusions having a particle size of less than 4 ⁇ m was calculated. Inclusions having a long side of less than 2 ⁇ m were not analyzed.
- a sulfide stress corrosion cracking test was performed in accordance with the test method specified in NACE TM TM0177 Method A.
- the tensile test piece described above was prepared using the test solution: (acetic acid-sodium acetate aqueous solution containing 5.0 mass% saline solution saturated with 10 kPa hydrogen sulfide and adjusted to pH 3.5 (liquid temperature: 24 °C)), and a constant load test that holds 85% of the yield strength YS under stress. If it did not break by 720h, the test was “O” (passed), and it broke by 720h. The case was evaluated as “x” (failed). In addition, when the target yield strength could not be secured, the sulfide stress corrosion cracking test was not performed.
- All the examples of the present invention are seamless steel pipes having both high strength of yield strength YS: 862 MPa and excellent SSC resistance.
- the yield strength YS is lowered and the desired high strength cannot be secured, or the SSC resistance is lowered.
Abstract
Description
(1)質量%で、C:0.20~0.50%、Si:0.05~0.40%、Mn:0.3~0.9%、P:0.015%以下、S:0.005%以下、Al:0.005~0.1%、N:0.006%以下、Cr:0.6%超え1.7%以下、Mo:1.0%超え3.0%以下、V:0.02~0.3%、Nb:0.001~0.02%、B:0.0003~0.0030%、O(酸素):0.0030%以下、Ti:0.003~0.025%を含み、かつTi、NをTi/N:2.0~5.0を満足するように含有し、残部Feおよび不可避的不純物からなる組成を有し、焼戻マルテンサイトを体積率で95%以上とし、旧オーステナイト粒が粒度番号で8.5以上であり、圧延方向に垂直な断面において、粒径が4μm以上の窒化物系介在物が100mm2あたり100個以下、粒径が4μm未満の窒化物系介在物が100mm2あたり1000個以下、粒径が4μm以上の酸化物系介在物が100mm2あたり40個以下、粒径が4μm未満の酸化物系介在物が100mm2あたり400個以下である組織を有する、降伏強さYS:862MPa以上である油井用高強度継目無鋼管。
(2)(1)において、前記組成に加えてさらに、質量%で、Cu:1.0%以下、Ni:1.0%以下、W:3.0%以下のうちから選ばれた1種または2種以上を含有する組成とする油井用高強度継目無鋼管。
(3)(1)または(2)において、前記組成に加えてさらに、質量%で、Ca:0.0005~0.0050%を含有する組成とする油井用高強度継目無鋼管。
(4)鋼管素材を加熱し、熱間加工を施して所定形状の継目無鋼管とする油井用継目無鋼管の製造方法であって、(1)ないし(3)のいずれかに記載の油井用高強度継目無鋼管の製造方法であり、前記加熱の加熱温度を、1050~1350℃の範囲の温度とし、前記熱間加工後に、前記継目無鋼管に空冷以上の冷却速度で表面温度が200℃以下となる温度まで冷却を施し、該冷却後、Ac3変態点以上1000℃以下の範囲の温度に再加熱し、表面温度で200℃以下となる温度まで急冷する焼入れ処理を1回以上施し、前記焼入れ処理後600~740℃の範囲の温度に加熱する焼戻処理を施す油井用高強度継目無鋼管の製造方法。
Cは、固溶して鋼の強度増加に寄与するとともに、鋼の焼入性を向上させ、焼入れ時にマルテンサイト相を主相とする組織の形成に寄与する。このような効果を得るためには、Cは0.20%以上の含有を必要とする。一方、Cの0.50%を超える含有は、焼入れ時に割れを発生させ、製造性を著しく低下させる。このため、Cは0.20~0.50%の範囲に限定した。なお、好ましくは、Cは0.20~0.35%である。より好ましくは、Cは0.22~0.32%である。
Siは、脱酸剤として作用するとともに、鋼中に固溶して鋼の強度を増加させ、さらに焼戻時の軟化を抑制する作用を有する元素である。このような効果を得るためには、Siは0.05%以上含有する必要がある。一方、Siの0.40%を超える多量の含有は、軟化相であるフェライト相の生成を促進し、所望の高強度化を阻害したり、さらに粗大な酸化物系介在物の形成を促進して、耐SSC性や靭性を低下させる。また、Siは偏析して局部的に鋼を硬化させる元素であり、多量の含有は、局部的硬化領域を形成し、耐SSC性を低下させるという悪影響をおよぼす。このようなことから、本発明では、Siは0.05~0.40%の範囲に限定した。なお、好ましくは、Siは0.05~0.30%である。より好ましくは、Siは0.20~0.30%である。
Mnは、Cと同様に、鋼の焼入性を向上させ、鋼の強度増加に寄与する元素である。このような効果を得るためには、Mnは0.3%以上の含有を必要とする。一方、Mnは、偏析して局部的に鋼を硬化させる元素であり、多量のMnの含有は、局部的硬化領域を形成し、耐SSC性を低下させるという悪影響をおよぼす。このため、本発明では、Mnは0.3~0.9%の範囲に限定した。なお、好ましくは、Mnは0.4~0.8%である。より好ましくは、Mnは0.5~0.8%である。
Pは、粒界に偏析して粒界脆化を引き起こすだけでなく、偏析して局部的に鋼を硬化させる元素であり、本発明では、Pは不可避的不純物として、できるだけ低減することが好ましいが、0.015%までは許容できる。このため、Pは0.015%以下に限定した。なお、好ましくは、Pは0.012%以下である。
Sは、不可避的不純物として、鋼中ではそのほとんどが硫化物系介在物として存在し、延性、靭性、さらには耐SSC性を低下させるため、できるだけ低減することが好ましいが、0.005%までは許容できる。このため、Sは0.005%以下に限定した。なお、好ましくは、Sは0.003%以下である。
Alは、脱酸剤として作用するとともに、Nと結合してAlNを形成して、加熱時のオーステナイト粒の微細化に寄与する。また、Alは、Nを固定し、固溶BがNと結合するのを防止して、Bの焼入性向上効果の低減を抑制する。このような効果を得るためには、Alは0.005%以上の含有を必要とする。一方、0.1%を超えるAlの含有は、酸化物系介在物の増加をもたらし、鋼の清浄度を低下させて、延性、靭性、さらには耐SSC性の低下を招く。このため、Alは0.005~0.1%の範囲に限定した。なお、好ましくは、Alは0.01~0.08%である。より好ましくは、Alは0.02~0.05%である。
Nは、不可避的不純物として鋼中に存在するが、Alと結合してAlNを形成し、また、Tiを含有する場合はTiNを形成して、結晶粒を微細化し、靭性を向上させる作用を有する。しかし、0.006%を超えるNの含有は、形成される窒化物が粗大化し、耐SSC性や靭性を著しく低下させる。このため、Nは0.006%以下に限定した。
Crは、焼入性の向上を介して鋼の強度を増加させるとともに、耐食性を向上させる元素である。また、Crは、焼戻処理時にCと結合し、M3C、M7C3、M23C6(Mは金属元素)などの炭化物を形成し、焼戻軟化抵抗を向上させる元素であり、とくに鋼管の高強度化に際しては必要な元素である。特にM3C型炭化物は、焼戻軟化抵抗を向上させる作用が強い。このような効果を得るためには、Crは0.6%超えの含有を必要とする。一方、1.7%を超えてCrを含有すると、多量のM7C3、M23C6を形成し、水素のトラップサイトとして作用して耐SSC性を低下させる。このようなことから、Crは、0.6%超え1.7%以下の範囲に限定した。なお、好ましくは、Crは0.8~1.5%である。より好ましくは、Crは0.8~1.3%である。
Moは、炭化物を形成し、析出強化により鋼の強化に寄与する元素であり、焼戻により転位密度を低減させたうえで所望の高強度を確保するのに有効に寄与する。転位密度の低減により耐SSC性が向上する。また、Moは、鋼中に固溶して、旧オーステナイト粒界に偏析して、耐SSC性の向上に寄与する。さらに、Moは、腐食生成物を緻密化し、さらに割れの起点となるピットの生成・成長を抑制する作用を有する。このような効果を得るためには、Moは1.0%超えの含有を必要とする。一方、3.0%を超えるMoの含有は、針状のM2C析出物や、場合によってはLaves相(Fe2Mo)の形成を促進して、耐SSC性を低下させる。このため、Moは1.0%超え3.0%以下の範囲に限定した。なお、好ましくは、Moは、1.1%超え3.0%以下、より好ましくは、1.2%超え2.8%以下、さらに好ましくは、1.45~2.5%である。より好ましくは、Moは1.45~1.80%である。
Vは、炭化物や炭窒化物を形成し、鋼の強化に寄与する元素である。このような効果を得るためには、Vは0.02%以上の含有を必要とする。一方、0.3%を超えてVを含有しても、効果が飽和し、含有量に見合う効果を期待できなくなり、経済的に不利となる。このため、Vは0.02~0.3%の範囲に限定した。なお、好ましくは0.03~0.20%、さらに好ましくは、Vは0.15%以下である。
Nbは、炭化物やあるいはさらに炭窒化物を形成し、析出強化により鋼の強度増加に寄与するとともに、オーステナイト粒の微細化にも寄与する。このような効果を得るためには、Nbは0.001%以上の含有を必要とする。一方、Nb析出物は、SSC(硫化物応力腐食割れ)の伝播経路と成りやすく、0.02%を超える多量のNb含有に基づく多量のNb析出物の存在は、とくに降伏強さ125ksi以上の高強度鋼材において、耐SSC性の顕著な低下に繋がる。このため、所望の高強度と優れた耐SSC性との両立の観点から、本発明では、Nbは0.001~0.02%に限定した。なお、好ましくは、Nbは0.001%以上、0.01%未満である。
Bは、オーステナイト粒界に偏析し、粒界からのフェライト変態を抑制することにより、微量の含有でも、鋼の焼入性を高める作用を有する。このような効果を得るためには、Bは0.0003%以上の含有を必要とする。一方、0.0030%超えてBを含有すると、炭窒化物等として析出し、焼入性が低下し、したがって靭性が低下する。このため、Bは0.0003~0.0030%の範囲に限定した。なお、好ましくは、Bは0.0007~0.0025%である。
O(酸素)は、不可避的不純物として、鋼中では酸化物系介在物として存在している。これら介在物は、SSCの発生起点となり、耐SSC性を低下させるため、本発明ではO(酸素)は、できるだけ低減することが好ましい。しかし、過剰な低減は精錬コストの高騰を招くため、0.0030%までは許容できる。このため、O(酸素)は0.0030%以下に限定した。なお、好ましくは、Oは0.0020%以下である。
Tiは、溶鋼の凝固時にNと結合し微細なTiNとして析出して、そのピンニング効果により、オーステナイト粒の微細化に寄与する。このような効果を得るためには、Tiは0.003%以上の含有を必要とする。Tiは0.003%未満の含有ではその効果が小さい。一方、Tiを0.025%を超えて含有すると、TiNが粗大化し、上記したピンニング効果が発揮できず、かえって靭性が低下する。また、さらに粗大なTiNが起因となり、耐SSC性が低下する。このようなことから、Tiは0.003~0.025%の範囲に限定した。
Ti/Nが2.0未満では、Nの固定が不足しBNを形成し、Bによる焼入性向上効果が低下する。一方、Ti/Nが5.0を超えて大きい場合には、TiNが粗大化する傾向が顕著になり、靭性や耐SSC性が低下する。このようなことから、Ti/Nは2.0~5.0の範囲に限定した。なお、好ましくは、Ti/Nは2.5~4.5である。
Cu、Ni、Wはいずれも、鋼の強度増加に寄与する元素であり、必要に応じて1種または2種以上を選択して含有できる。
Caは、Sと結合しCaSを形成して、硫化物系介在物の形態制御に有効に作用する元素であり、硫化物系介在物の形態制御を介して、靭性、耐SSC性の向上に寄与する。このような効果を得るためには、Caは少なくとも0.0005%の含有を必要とする。一方、Caを0.005%を超えて含有しても、その効果が飽和し、含有量に見合う効果が期待できなくなり、経済性に不利となる。このため、Caを含有する場合には、Caは0.0005~0.005%の範囲に限定することが好ましい。
本発明の高強度継目無鋼管では、YS:125ksi級以上の高強度を確保するためと構造物として必要な延性や靭性を保持するために、マルテンサイト相を焼戻した焼戻マルテンサイト相を主相とする。ここでいう「主相」とは、当該相が体積率で100%である単相である場合、あるいは第二相を特性に影響しない程度である体積率で5%以下含む、当該相が95%以上である場合をいう。なお、本発明では、第二相は、ベイナイト相、残留オーステナイト相、パーライトあるいはそれらの混合相が例示できる。
旧オーステナイト粒の粒度番号が8.5未満では、生成するマルテンサイト相の下部組織が粗大化し、耐SSC性が低下する。このため、旧オーステナイト粒の粒度番号を8.5以上に限定した。なお、粒度番号は、JIS G 0551の規定に準拠して測定した値を用いるものとする。
窒化物系介在物は、降伏強さ125ksi級以上の高強度鋼管ではSSCの発生起点となり、その大きさが4μm以上と大きくなるほど、その悪影響が大きくなる。そのため、4μm以上の窒化物系介在物はできるだけ、少なくすることが望ましいが、100mm2あたり100個以下であれば、耐SSC性への悪影響は許容できる。このため、粒径が4μm以上の窒化物系介在物は100mm2あたり100個以下に限定した。なお、好ましくは84個以下である。
粒径が4μm未満の微細な窒化物系介在物は、単独で存在してもSSCの発生起点にはならないが、降伏強さYS:125ksi級以上の高強度鋼管では、その数が多くなり、100mm2あたり1000個を超えると、耐SSC性への悪影響が許容できなくなる。このため、粒径が4μm未満の窒化物系介在物は100mm2あたり1000個以下に限定した。なお、好ましくは900個以下である。
酸化物系介在物は、降伏強さYS:125ksi級以上の高強度鋼管では、SSCの発生起点となり、その大きさが4μm以上と大きくなるほど、その悪影響が大きくなる。そこで、粒径が4μm以上の酸化物系介在物はできるだけ、少なくすることが望ましいが、100mm2あたり40個以下であれば、耐SSC性への悪影響は許容できる。このため、粒径が4μm以上の酸化物系介在物は100mm2あたり40個以下に限定した。なお、好ましくは35個以下である。
酸化物系介在物は、降伏強さ125ksi級以上の高強度鋼では、粒径が4μm未満と小さいものでもSSCの発生起点となり、その数が多くなるほど耐SSC性への悪影響が大きくなる。そのため、粒径が4μm未満の酸化物系介在物でもできるだけ少なくすることが望ましいが、100mm2あたり400個以下であれば、許容できる。このようなことから、粒径が4μm未満の酸化物系介在物は100mm2あたり400個以下に限定した。なお、好ましくは365個以下である。
加熱温度が1050℃未満では、鋼管素材中の炭化物の溶解が不十分となる。一方、1350℃を超えて加熱されると、結晶粒が粗大化するとともに、凝固時に析出したTiNなどの析出物が粗大化し、また、セメンタイトが粗大化するため、鋼管靭性が低下する。また、1350℃を超える高温に加熱すると、鋼管素材表面にスケール層が厚く生成し、圧延時に表面疵等の発生原因になるとともに、エネルギーロスが増大し省エネルギーの観点から好ましくない。このようなことから、加熱温度は1050~1350℃の範囲の温度に限定した。なお、好ましくは1100~1300℃である。
本発明の組成範囲では、熱間加工後に空冷以上の冷却速度で冷却すれば、マルテンサイト相を主相とする組織を得ることができる。表面温度が200℃超えで空冷(冷却)を停止すると、変態が完全に完了していない場合がある。そのため、熱間加工後の冷却処理は、表面温度が200℃以下となるまで、空冷以上の冷却速度で冷却することとした。また、本発明において、「空冷以上の冷却速度」とは、0.1℃/s以上のことを指す。0.1℃/s未満の冷却速度であると、冷却後の金属組織が不均一になり、その後の熱処理後の金属組織が不均一となる。
焼戻処理は、転位密度を減少させ、靭性および耐SSC性を向上させる目的で行なう。焼戻温度が600℃未満では、転位の減少が不十分であるため、優れた耐SSC性を確保できない。一方、740℃を超える温度では、組織の軟化が著しく、所望の高強度を確保できない。このため、焼戻温度は600~740℃の範囲の温度に限定した。なお、好ましくは660~710℃である。
再加熱温度が、Ac3変態点未満では、オーステナイト単相域に加熱されないため、マルテンサイト相を主相とする組織が得られない。一方、1000℃を超えると、結晶粒が粗大化し靭性が低下することに加え、表面の酸化スケールが厚くなり、剥離しやすくなり鋼板表面の疵発生の原因となる、などの悪影響がある。さらに、熱処理炉への負荷が過大となり、省エネルギーの観点からも問題となる。このようなことから、また、省エネルギーの観点から、焼入れ処理のための再加熱温度は、Ac3変態点以上1000℃以下に限定した。なお、好ましくは950℃以下である。
(ここで、C、Si、Mn、Cu、Cr、Ni、Mo、V、Ti、Al、B:各元素の含有量(質量%))
Ac3変態点の計算にあたっては、上記した式に記載された元素を含有しない場合には、当該元素の含有量を零%として算出するものとする。
(1)組織観察
得られた継目無鋼管の、内面側1/4t位置(t:管厚)から組織観察用試験片を採取し、管長手方向に直交する断面(C断面)を研磨し、腐食(ナイタール(nital(硝酸-エタノール混合液))腐食)して組織を現出させ、光学顕微鏡(倍率:1000倍)および走査型電子顕微鏡(倍率:2000~3000倍)を用いて、組織を観察し、視野:4箇所以上で撮像した。得られた組織写真に基づき、画像解析により、構成する相の同定、およびそれら相の組織分率を、それぞれ算出した。
また、介在物として識別した粒子の個数を求め、さらに各粒子の面積を求め、円相当直径を計算し当該介在物の粒径とした。そして、粒径:4μm以上の介在物と粒径:4μm未満の介在物の個数密度(個/100mm2)を算出した。なお、長辺が2μmに満たない介在物は分析しなかった。
得られた継目無鋼管の内面側1/4t位置(t:管厚)から、JIS Z 2241の規定に準拠して、引張方向が管軸方向となるように、JIS 10号引張試験片(棒状試験片:平行部径12.5mmφ、平行部長さ:60mm、GL:50mm)を採取し、引張試験を実施し、引張特性(降伏強さYS(0.5%耐力))、引張強さTS)を求めた。
(3)硫化物応力腐食割れ試験
得られた継目無鋼管の内面側1/4t位置(t:管厚)を中心として、管軸方向が引張方向となるように引張試験片(平行部径:6.35mmφ×平行部長さ25.4mm)を採取した。
Claims (4)
- 質量%で、
C :0.20~0.50%、 Si:0.05~0.40%、
Mn:0.3~0.9%、 P :0.015%以下、
S :0.005%以下、 Al:0.005~0.1%、
N :0.006%以下、 Cr:0.6%超え1.7%以下、
Mo:1.0%超え3.0%以下、 V :0.02~0.3%、
Nb:0.001~0.02%、 B :0.0003~0.0030%、
O(酸素):0.0030%以下、 Ti:0.003~0.025%
を含み、かつTi、NをTi/N:2.0~5.0を満足するように含有し、残部Feおよび不可避的不純物からなる組成を有し、焼戻マルテンサイトを体積率で95%以上とし、旧オーステナイト粒が粒度番号で8.5以上であり、圧延方向に垂直な断面において、粒径が4μm以上の窒化物系介在物が100mm2あたり100個以下、粒径が4μm未満の窒化物系介在物が100mm2あたり1000個以下、粒径が4μm以上の酸化物系介在物が100mm2あたり40個以下、粒径が4μm未満の酸化物系介在物が100mm2あたり400個以下である組織を有する、降伏強さYS:862MPa以上である油井用高強度継目無鋼管。 - 前記組成に加えてさらに、質量%で、Cu:1.0%以下、Ni:1.0%以下、W:3.0%以下のうちから選ばれた1種または2種以上を含有する請求項1に記載の油井用高強度継目無鋼管。
- 前記組成に加えてさらに、質量%で、Ca:0.0005~0.005%を含有する請求項1または2に記載の油井用高強度継目無鋼管。
- 鋼管素材を加熱し、熱間加工を施して所定形状の継目無鋼管とする油井用継目無鋼管の製造方法であって、請求項1ないし3のいずれかに記載の油井用高強度継目無鋼管の製造方法であり、
前記加熱の加熱温度を、1050~1350℃の範囲の温度とし、
前記熱間加工後に、前記継目無鋼管に空冷以上の冷却速度で表面温度が200℃以下となる温度まで冷却を施し、該冷却後、Ac3変態点以上1000℃以下の範囲の温度に再加熱し、表面温度で200℃以下となる温度まで急冷する焼入れ処理を1回以上施し、前記焼入れ処理後600~740℃の範囲の温度に加熱する焼戻処理を施す油井用高強度継目無鋼管の製造方法。
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
RU2017117289A RU2661972C1 (ru) | 2014-11-18 | 2015-08-20 | Высокопрочная бесшовная стальная труба для трубных изделий нефтепромыслового сортамента и способ ее изготовления |
US15/527,893 US10920297B2 (en) | 2014-11-18 | 2015-08-20 | High-strength seamless steel pipe for oil country tubular goods and method of producing the same |
JP2015559379A JP5930140B1 (ja) | 2014-11-18 | 2015-08-20 | 油井用高強度継目無鋼管およびその製造方法 |
EP15860191.4A EP3222740B1 (en) | 2014-11-18 | 2015-08-20 | High-strength seamless steel pipe for oil wells and method for producing same |
MX2017006430A MX2017006430A (es) | 2014-11-18 | 2015-08-20 | Tuberia de acero sin costura de alta resistencia para productos tubulares para campos petroleros y metodo para producir los mismos. |
BR112017009632-3A BR112017009632B1 (pt) | 2014-11-18 | 2015-08-20 | tubo de aço sem costura de alta resistência para produtos tubulares para indústria petrolífera e método para produzir o mesmo |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2014233682 | 2014-11-18 | ||
JP2014-233682 | 2014-11-18 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2016079908A1 true WO2016079908A1 (ja) | 2016-05-26 |
Family
ID=56013488
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2015/004182 WO2016079908A1 (ja) | 2014-11-18 | 2015-08-20 | 油井用高強度継目無鋼管およびその製造方法 |
Country Status (8)
Country | Link |
---|---|
US (1) | US10920297B2 (ja) |
EP (1) | EP3222740B1 (ja) |
JP (1) | JP5930140B1 (ja) |
AR (1) | AR101763A1 (ja) |
BR (1) | BR112017009632B1 (ja) |
MX (1) | MX2017006430A (ja) |
RU (1) | RU2661972C1 (ja) |
WO (1) | WO2016079908A1 (ja) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2018074109A1 (ja) | 2016-10-17 | 2018-04-26 | Jfeスチール株式会社 | 油井用高強度継目無鋼管およびその製造方法 |
EP3733890A4 (en) * | 2017-12-26 | 2020-11-04 | JFE Steel Corporation | HIGH STRENGTH SEAMLESS LOW ALLOY STEEL TUBE FOR OIL WELLS |
EP3733896A4 (en) * | 2017-12-26 | 2020-11-04 | JFE Steel Corporation | HIGH STRENGTH, LOW ALLOY, SEAMLESS STEEL PIPE, INTENDED FOR OIL WELLS |
JPWO2020166668A1 (ja) * | 2019-02-15 | 2021-10-14 | 日本製鉄株式会社 | サワー環境での使用に適した鋼材 |
JPWO2021131461A1 (ja) * | 2019-12-26 | 2021-12-23 | Jfeスチール株式会社 | 高強度継目無鋼管およびその製造方法 |
US11505842B2 (en) | 2017-12-26 | 2022-11-22 | Jfe Steel Corporation | Low-alloy high-strength seamless steel pipe for oil country tubular goods |
Families Citing this family (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
MX2017002975A (es) | 2014-09-08 | 2017-06-19 | Jfe Steel Corp | Tuberia de acero sin costura de alta resistencia para productos tubulares de region petrolifera y metodo de produccion de la misma. |
CN106687614B (zh) * | 2014-09-08 | 2019-04-30 | 杰富意钢铁株式会社 | 油井用高强度无缝钢管及其制造方法 |
WO2016079908A1 (ja) | 2014-11-18 | 2016-05-26 | Jfeスチール株式会社 | 油井用高強度継目無鋼管およびその製造方法 |
EP3231884B1 (en) * | 2014-12-12 | 2021-08-18 | Nippon Steel Corporation | Low-alloy steel oil well pipe and method for manufacturing a low-alloy steel oil well pipe |
WO2016103538A1 (ja) | 2014-12-24 | 2016-06-30 | Jfeスチール株式会社 | 油井用高強度継目無鋼管およびその製造方法 |
BR112017012766B1 (pt) | 2014-12-24 | 2021-06-01 | Jfe Steel Corporation | Tubo de aço sem costura de alta resistência para produtos tubulares da indústria petrolífera e seu método de produção |
US11186885B2 (en) | 2015-12-22 | 2021-11-30 | Jfe Steel Corporation | High-strength seamless steel pipe for oil country tubular goods, and production method for high-strength seamless steel pipe for oil country tubular goods |
CN109868413A (zh) * | 2019-03-06 | 2019-06-11 | 天津钢管集团股份有限公司 | 110ksi钢级抗硫化物应力腐蚀钻杆接头用管的制造方法 |
CN113025902B (zh) * | 2021-03-04 | 2022-02-01 | 东北大学 | 一种强韧性能优良的热轧无缝钢管及其制造方法 |
CN113025904B (zh) * | 2021-03-04 | 2022-02-01 | 东北大学 | 一种热轧无缝钢管及其形变相变一体化组织调控方法 |
CN117305684A (zh) * | 2022-06-22 | 2023-12-29 | 宝山钢铁股份有限公司 | 一种加工性能良好的电机轴用高强韧无缝钢管及其制造方法 |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001172739A (ja) * | 1999-12-15 | 2001-06-26 | Sumitomo Metal Ind Ltd | 耐硫化物応力腐食割れ性に優れた油井用鋼材およびそれを用いた油井用鋼管の製造方法 |
WO2006009142A1 (ja) * | 2004-07-20 | 2006-01-26 | Sumitomo Metal Industries, Ltd. | 鋼管用鋼 |
WO2010150915A1 (ja) * | 2009-06-24 | 2010-12-29 | Jfeスチール株式会社 | 耐硫化物応力割れ性に優れた油井用高強度継目無鋼管およびその製造方法 |
WO2013191131A1 (ja) * | 2012-06-20 | 2013-12-27 | 新日鐵住金株式会社 | 油井管用鋼及びその製造方法 |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS52152814A (en) * | 1976-06-14 | 1977-12-19 | Nippon Steel Corp | Thermo-mechanical treatment of seamless steel pipe |
JP3562353B2 (ja) | 1998-12-09 | 2004-09-08 | 住友金属工業株式会社 | 耐硫化物応力腐食割れ性に優れる油井用鋼およびその製造方法 |
JP4058840B2 (ja) | 1999-04-09 | 2008-03-12 | 住友金属工業株式会社 | 靭性と耐硫化物応力腐食割れ性に優れる油井用鋼およびその製造方法 |
JP3969328B2 (ja) | 2003-03-26 | 2007-09-05 | 住友金属工業株式会社 | 非調質継目無鋼管 |
EP1652950B1 (en) * | 2003-07-22 | 2014-10-15 | Nippon Steel & Sumitomo Metal Corporation | Martensitic stainless steel |
RU2288967C1 (ru) * | 2005-04-15 | 2006-12-10 | Закрытое акционерное общество ПКФ "Проммет-спецсталь" | Коррозионно-стойкий сплав и изделие, выполненное из него |
JP4725216B2 (ja) | 2005-07-08 | 2011-07-13 | 住友金属工業株式会社 | 耐硫化物応力割れ性に優れた低合金油井管用鋼 |
EP1918397B1 (en) | 2005-08-22 | 2016-07-20 | Nippon Steel & Sumitomo Metal Corporation | Seamless steel pipe for pipe line and method for producing same |
WO2008123425A1 (ja) | 2007-03-30 | 2008-10-16 | Sumitomo Metal Industries, Ltd. | 低合金油井管用鋼および継目無鋼管 |
FR2942808B1 (fr) | 2009-03-03 | 2011-02-18 | Vallourec Mannesmann Oil & Gas | Acier faiblement allie a limite d'elasticite elevee et haute resistance a la fissuration sous contrainte par les sulfures. |
JP5505100B2 (ja) * | 2010-06-04 | 2014-05-28 | Jfeスチール株式会社 | 炭酸ガスインジェクション用部材向けCr含有鋼管 |
JP2013129879A (ja) | 2011-12-22 | 2013-07-04 | Jfe Steel Corp | 耐硫化物応力割れ性に優れた油井用高強度継目無鋼管およびその製造方法 |
EP2824198B8 (en) | 2012-03-07 | 2020-04-15 | Nippon Steel Corporation | Method for producing seamless steel pipe having high-strength and excellent sulfide stress cracking resistance |
JP6107437B2 (ja) | 2012-06-08 | 2017-04-05 | Jfeスチール株式会社 | 耐硫化物応力腐食割れ性に優れた油井用低合金高強度継目無鋼管の製造方法 |
MX2017002975A (es) | 2014-09-08 | 2017-06-19 | Jfe Steel Corp | Tuberia de acero sin costura de alta resistencia para productos tubulares de region petrolifera y metodo de produccion de la misma. |
WO2016079908A1 (ja) | 2014-11-18 | 2016-05-26 | Jfeスチール株式会社 | 油井用高強度継目無鋼管およびその製造方法 |
WO2016103538A1 (ja) | 2014-12-24 | 2016-06-30 | Jfeスチール株式会社 | 油井用高強度継目無鋼管およびその製造方法 |
BR112017012766B1 (pt) | 2014-12-24 | 2021-06-01 | Jfe Steel Corporation | Tubo de aço sem costura de alta resistência para produtos tubulares da indústria petrolífera e seu método de produção |
US11186885B2 (en) | 2015-12-22 | 2021-11-30 | Jfe Steel Corporation | High-strength seamless steel pipe for oil country tubular goods, and production method for high-strength seamless steel pipe for oil country tubular goods |
-
2015
- 2015-08-20 WO PCT/JP2015/004182 patent/WO2016079908A1/ja active Application Filing
- 2015-08-20 JP JP2015559379A patent/JP5930140B1/ja active Active
- 2015-08-20 BR BR112017009632-3A patent/BR112017009632B1/pt active IP Right Grant
- 2015-08-20 EP EP15860191.4A patent/EP3222740B1/en active Active
- 2015-08-20 MX MX2017006430A patent/MX2017006430A/es unknown
- 2015-08-20 RU RU2017117289A patent/RU2661972C1/ru active
- 2015-08-20 US US15/527,893 patent/US10920297B2/en active Active
- 2015-09-04 AR ARP150102832A patent/AR101763A1/es active IP Right Grant
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001172739A (ja) * | 1999-12-15 | 2001-06-26 | Sumitomo Metal Ind Ltd | 耐硫化物応力腐食割れ性に優れた油井用鋼材およびそれを用いた油井用鋼管の製造方法 |
WO2006009142A1 (ja) * | 2004-07-20 | 2006-01-26 | Sumitomo Metal Industries, Ltd. | 鋼管用鋼 |
WO2010150915A1 (ja) * | 2009-06-24 | 2010-12-29 | Jfeスチール株式会社 | 耐硫化物応力割れ性に優れた油井用高強度継目無鋼管およびその製造方法 |
WO2013191131A1 (ja) * | 2012-06-20 | 2013-12-27 | 新日鐵住金株式会社 | 油井管用鋼及びその製造方法 |
Cited By (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPWO2018074109A1 (ja) * | 2016-10-17 | 2018-10-18 | Jfeスチール株式会社 | 油井用高強度継目無鋼管およびその製造方法 |
EP3527684A4 (en) * | 2016-10-17 | 2019-08-21 | JFE Steel Corporation | HIGH RESISTANCE SOLDERED STEEL PIPE FOR OIL WELLS AND PROCESS FOR PRODUCING THE SAME |
WO2018074109A1 (ja) | 2016-10-17 | 2018-04-26 | Jfeスチール株式会社 | 油井用高強度継目無鋼管およびその製造方法 |
US11313007B2 (en) | 2016-10-17 | 2022-04-26 | Jfe Steel Corporation | High-strength seamless steel pipe for oil country tubular goods, and method for producing the same |
US11453924B2 (en) | 2017-12-26 | 2022-09-27 | Jfe Steel Corporation | Low-alloy high-strength seamless steel pipe for oil country tubular goods |
EP3733890A4 (en) * | 2017-12-26 | 2020-11-04 | JFE Steel Corporation | HIGH STRENGTH SEAMLESS LOW ALLOY STEEL TUBE FOR OIL WELLS |
EP3733896A4 (en) * | 2017-12-26 | 2020-11-04 | JFE Steel Corporation | HIGH STRENGTH, LOW ALLOY, SEAMLESS STEEL PIPE, INTENDED FOR OIL WELLS |
US11505842B2 (en) | 2017-12-26 | 2022-11-22 | Jfe Steel Corporation | Low-alloy high-strength seamless steel pipe for oil country tubular goods |
US11414733B2 (en) | 2017-12-26 | 2022-08-16 | Jfe Steel Corporation | Low-alloy high-strength seamless steel pipe for oil country tubular goods |
JPWO2020166668A1 (ja) * | 2019-02-15 | 2021-10-14 | 日本製鉄株式会社 | サワー環境での使用に適した鋼材 |
JP7036237B2 (ja) | 2019-02-15 | 2022-03-15 | 日本製鉄株式会社 | サワー環境での使用に適した鋼材 |
JPWO2021131461A1 (ja) * | 2019-12-26 | 2021-12-23 | Jfeスチール株式会社 | 高強度継目無鋼管およびその製造方法 |
JP7095801B2 (ja) | 2019-12-26 | 2022-07-05 | Jfeスチール株式会社 | 高強度継目無鋼管およびその製造方法 |
Also Published As
Publication number | Publication date |
---|---|
US20180327881A1 (en) | 2018-11-15 |
MX2017006430A (es) | 2017-09-12 |
BR112017009632A2 (pt) | 2017-12-19 |
JPWO2016079908A1 (ja) | 2017-04-27 |
BR112017009632B1 (pt) | 2021-05-04 |
RU2661972C1 (ru) | 2018-07-23 |
US10920297B2 (en) | 2021-02-16 |
EP3222740B1 (en) | 2020-03-11 |
AR101763A1 (es) | 2017-01-11 |
EP3222740A1 (en) | 2017-09-27 |
EP3222740A4 (en) | 2017-10-18 |
JP5930140B1 (ja) | 2016-06-08 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP5930140B1 (ja) | 油井用高強度継目無鋼管およびその製造方法 | |
JP5943165B1 (ja) | 油井用高強度継目無鋼管およびその製造方法 | |
JP5943164B1 (ja) | 油井用高強度継目無鋼管およびその製造方法 | |
JP5971435B1 (ja) | 油井用高強度継目無鋼管およびその製造方法 | |
WO2017110027A1 (ja) | 油井用高強度継目無鋼管およびその製造方法 | |
JP6451874B2 (ja) | 油井用高強度継目無鋼管およびその製造方法 | |
KR101892839B1 (ko) | 후강판 및 그 제조 방법 | |
WO2015019708A1 (ja) | ラインパイプ用継目無鋼管およびその製造方法 | |
JP6075507B2 (ja) | ラインパイプ用継目無鋼管およびその製造方法 | |
JP5971436B1 (ja) | 油井用高強度継目無鋼管およびその製造方法 | |
JP6128297B1 (ja) | 油井用高強度継目無鋼管およびその製造方法 | |
WO2019180499A1 (en) | A steel composition in accordance with api 5l psl-2 specification for x-65 grade having enhanced hydrogen induced cracking (hic) resistance, and method of manufacturing the steel thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ENP | Entry into the national phase |
Ref document number: 2015559379 Country of ref document: JP Kind code of ref document: A |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 15860191 Country of ref document: EP Kind code of ref document: A1 |
|
REEP | Request for entry into the european phase |
Ref document number: 2015860191 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: MX/A/2017/006430 Country of ref document: MX |
|
ENP | Entry into the national phase |
Ref document number: 2017117289 Country of ref document: RU Kind code of ref document: A |
|
NENP | Non-entry into the national phase |
Ref country code: DE |
|
WWE | Wipo information: entry into national phase |
Ref document number: 15527893 Country of ref document: US |
|
REG | Reference to national code |
Ref country code: BR Ref legal event code: B01A Ref document number: 112017009632 Country of ref document: BR |
|
ENP | Entry into the national phase |
Ref document number: 112017009632 Country of ref document: BR Kind code of ref document: A2 Effective date: 20170508 |