WO2013002418A1 - 耐サワー性に優れたラインパイプ用厚肉高強度継目無鋼管およびその製造方法 - Google Patents
耐サワー性に優れたラインパイプ用厚肉高強度継目無鋼管およびその製造方法 Download PDFInfo
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- WO2013002418A1 WO2013002418A1 PCT/JP2012/067254 JP2012067254W WO2013002418A1 WO 2013002418 A1 WO2013002418 A1 WO 2013002418A1 JP 2012067254 W JP2012067254 W JP 2012067254W WO 2013002418 A1 WO2013002418 A1 WO 2013002418A1
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- 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
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- 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
- C21D1/25—Hardening, combined with annealing between 300 degrees Celsius and 600 degrees Celsius, i.e. heat refining ("Vergüten")
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- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
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- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/24—Ferrous alloys, e.g. steel alloys containing chromium with vanadium
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- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
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- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
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- 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
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- 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
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- 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
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- 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
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- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
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- 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
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- 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
- C22C38/58—Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
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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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- 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
- C21D1/62—Quenching devices
- C21D1/63—Quenching devices for bath quenching
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- 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
- C21D2261/00—Machining or cutting being involved
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- 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
Definitions
- the present invention relates to a thick, high-strength seamless steel tube suitable for use in line pipes for transporting crude oil, natural gas, and the like, and is particularly resistant to sour resistance. It relates to the further improvement of the nature (sour resistance).
- the line pipe used is required to have strength to withstand water pressure and to sink under its own weight.
- the thickness of the line pipe to be used exceeds 20 mm, and in some cases, it may be a seamless steel pipe having a thickness of 35 mm or more.
- Such thick-walled seamless steel pipes are required to have higher strength, excellent corrosion resistance, and excellent circumferential weldability.
- Patent Document 1 and Patent Document 2 include C: 0.03 to 0.11%, Si: 0.05 to 0.5%, and Mn: 0.8 to 1.6. %, P: 0.025% or less, S: 0.003% or less, Ti: 0.002 to 0.017%, Al: 0.001 to 0.10%, Cr: 0.05 to 0.5% , Mo: 0.02 to 0.3%, V: 0.02 to 0.20%, Ca: 0.0005 to 0.005%, N: 0.008% or less, O: 0.004% or less
- a high-strength seamless steel pipe having a composition containing it and a structure in which ferrite is precipitated at grain boundaries of bainite and / or martensite is described.
- a steel slab having the above composition is formed into a seamless steel pipe by hot rolling, and (Ar3 point + 50 ° C.) to 1100 ° C. is used as a quenching start temperature, and is 5 ° C./s or more.
- tempering is then performed at 550 ° C. to Ac1 point, and hydrogen induced cracking resistance (hereinafter referred to as HIC resistance).
- HIC resistance hydrogen induced cracking resistance
- Patent Document 3 describes a method for producing a thick-walled seamless steel pipe for line pipes having high strength and good toughness.
- C 0.03 to 0.08%, Si: 0.25% or less, Mn: 0.3 to 2.5%, Al: 0.001 to 0.10% Cr: 0.02 to 1.0%, Ni: 0.02 to 1.0%, Mo: 0.02 to 1.2%, Ti: 0.004 to 0.010%, N: 0.002 ⁇ 0.008%, in total of one or more of Ca, Mg and REM: 0.0002 to 0.005%, V: 0 to 0.08%, Nb: 0 to 0.05% , A step of solidifying molten steel containing 0 to 1.0% into a billet having a round cross section by continuous casting, and an average cooling rate between 1400 to 1000 ° C.
- the step of cooling to room temperature at a rate of °C / min or more, the average heating rate between 550 °C and 900 °C is 15
- the steel tube is manufactured by piercing and rolling, immediately heated to 850 to 1000 ° C. immediately after the pipe making, or once cooled after the pipe making, and then 850
- a tempering process is sequentially performed at a temperature in the range of ° C.
- a round billet is formed by continuous casting into a square bloom or slab, and then forging or rolling. It is also good.
- the strength (hardness) of the steel pipe surface layer is unavoidable.
- a material having a C-Mn composition is used, and in cooling after rolling, quenching treatment such as water cooling (quenching treatment).
- quenching treatment such as water cooling (quenching treatment).
- the surface layer portion has a high cooling rate and is easy to be baked, so that the hardness becomes high. In some cases, it may become harder than a value determined by the API standard or DNV-OS-F101 standard.
- the cooling rate is slow, hard to be hardened, and a non-quenched metal structure such as ferrite may be mixed.
- a transformation characteristic in which a ferrite nose and a bainite nose are shifted to a short time side (transformation charactic)
- the cooling rate of the surface layer is 1000 ° C./second or more
- the wall thickness is 30 mm.
- the steel pipe has a cooling rate of about 20-30 ° C / second at the center of the wall thickness
- the surface layer has a hardened structure such as martensite and bainite. May contain non-quenched structures such as ferrite.
- the hardness distribution in the thickness direction is high in the vicinity of the surface layer, and the hardness distribution in the thickness direction is U-shaped as shown in FIG. Even if the hardness distribution in the thickness direction is subjected to a tempering treatment, the hardness level only decreases and does not disappear completely.
- the DNV-OS-F101 standard requires that the hardness at a position of 1.5 mm from the surface satisfy 250 HV10 or less. Even if the steel pipe has a hardness of 250 HV10 or less at a position of 1 mm or 5 mm from the surface, if the hardness of the outer surface layer is higher than 250 HV, it breaks in a highly corrosive environment. There is a case. In that case, it means that the steel pipe has reduced SSC resistance.
- An object of the present invention is to solve the problems of the prior art and to provide a thick high-strength seamless steel pipe excellent in sour resistance and a method for manufacturing the same.
- the “high-strength seamless steel pipe” here refers to a seamless steel pipe having a yield strength YS: exceeding 450 MPa (65 ksi).
- thick wall refers to the case where the wall thickness is 10 mm or more, preferably 15 mm or more, and more preferably 25 mm or more.
- sour resistance refers to characteristics including HIC resistance evaluated in accordance with NACE TM0284 and SSC resistance evaluated in accordance with NACE TM0177 or ASME G39.
- the present inventors diligently studied various factors affecting sour resistance in order to achieve the above-described object. As a result, it was found that the sour resistance is remarkably improved by suppressing the hardness of the portion (surface layer) in direct contact with the corrosive environment to a low level. Specifically, the Vickers hardness can be measured at a load of 5 kgf (test force: 49 N) and the outermost tube or the innermost tube (also referred to as the outermost layer of the tube) should be 250 HV5 or less. It has been found that it contributes significantly to the improvement of the property.
- the inventors have determined that the outer surface layer and the inner surface layer of the tube It was conceived that the hardness of the outermost layer of the pipe should be 250 HV5 or less by removing by applying pickling, shot blasting treatment, etc. or further grinding.
- the present inventors have found that the hardness distribution in the thickness direction is such that the hardness of the outermost layer is low and the maximum hardness exists at a certain depth from the surface, that is, as shown in FIG.
- the hardness of the outermost layer of the pipe should be 250 HV5 or less, as in Case 1, in order to significantly improve the sour resistance.
- the maximum hardness of the M-type distribution is also 250 HV5 or less, as in Case 2.
- the so-called M-type thickness direction hardness distribution has a heating temperature, holding time, and atmospheric gas at the time of hot rolling.
- surface decarburization by controlling the heating temperature, holding time, atmosphere gas, etc. during quenching, and further controlling the heating temperature, holding time, atmosphere gas, etc. during tempering, and
- the surface scale surface scale is formed during heat treatment, and the highest hardness part during quenching is scaled off (remove the area of maximum hardness as scale), or hardness by partial tempering of the surface layer only, etc.
- the area where hardness is reduced due to surface decarburization is an area from the outermost layer to about 2.5 to 3.0 mm. This is because when the hardness reduction region due to surface decarburization becomes thicker than about 2.5 to 3.0 mm from the outermost layer, particularly in the case of a thick material having a thickness of 20 mm or more, the steel pipe strength decreases due to decarburization. This is because the mechanical properties are affected. It is strongly affected when using an arc-formed tensile test piece as cutting out of pipe.
- the present invention has been completed on the basis of such findings and further studies. That is, the gist of the present invention is as follows. (1) Thickness, high-strength seamless steel pipe having a yield strength of more than 450 MPa, which has been subjected to quenching and tempering treatment, with a load of 5 kgf at the outermost pipe or innermost pipe (test) A thick, high-strength seamless steel pipe for line pipes having excellent sour resistance, characterized in that the Vickers hardness HV5 measurable at a force of 49 N) is 250 HV5 or less.
- the thickness distribution of the thick-walled high-strength seamless steel pipe in the entire thickness direction exhibits the M type, and the maximum hardness was measured at a load of 5 kgf (test force: 49 N).
- the seamless steel pipe is mass%, C: 0.03 to 0.15%, Si: 0.02 to 0.5%, Mn: 0 7 to 2.5%, P: 0.020% or less, S: 0.003% or less, Al: 0.01 to 0.08%, Ti: 0.005 to 0.05%, N: 0.0.
- Ti and N are represented by the following formula (1): N ⁇ Ti ⁇ 14/48 ⁇ N + 10 (1) (Here, Ti, N: content of each element (mass ppm))
- a thick-walled, high-strength seamless steel pipe for line pipes characterized by having a composition comprising the balance Fe and inevitable impurities.
- Cr 0.5% or less
- Mo 0.3% or less
- Ni 0.3% or less
- Cu 0.3% or less
- V 0.05% or less
- Nb One or more selected from 0.05% or less
- a method for producing a thick-walled, high-strength seamless steel pipe for a line pipe which is obtained by subjecting a raw steel pipe to a quenching treatment and a tempering treatment to yield a product steel pipe having a yield strength exceeding 450 MPa, % By mass, C: 0.03 to 0.15%, Si: 0.02 to 0.5%, Mn: 0.7 to 2.5%, P: 0.020% or less, S: 0.0.
- a raw steel pipe is subjected to a quenching treatment and a tempering treatment, and a yield strength: a manufacturing method of a thick high-strength seamless steel pipe for a line pipe to be a product steel pipe having a pressure exceeding 450 MPa
- the material steel pipe is, by mass%, C: 0.03-0.15%, Si: 0.02-0.5%, Mn: 0.7-2.5%, P: 0.020% or less, S: 0.003% or less, Al: 0.01 to 0.08%, Ti: 0.005 to 0.05%, N: 0.005% or less, and Ti and N are represented by the following formula (1) N ⁇ Ti ⁇ 14/48 ⁇ N + 10 (1) (Here, Ti, N: content of each element (mass ppm)) And a seamless steel pipe having a composition composed of the remaining Fe and inevitable impurities, and the quenching treatment is a treatment of heating and then quenching, and the heating is performed at an Ac3 transformation point in an air atmosphere.
- a method for producing a thick-walled, high-strength seamless steel pipe for line pipes with excellent sour resistance characterized in that the above-described heating temperature is maintained for 120 s or more, and the rapid cooling is water-cooling in a nucleate boiling state. .
- the rapid cooling is a process of water cooling in a nucleate boiling state after water cooling in a film boiling state instead of the process of water cooling in a nucleate boiling state.
- a method for manufacturing high-strength seamless steel pipes (11) In any one of (8) to (10), the heating is heating by any one of a heating furnace charging method, an electric heating method, or an induction heating method. Manufacturing method of high-strength seamless steel pipe.
- the thick-walled high-strength seamless steel pipe of the present invention is a thick-walled, high-strength seamless steel pipe having a yield strength exceeding 450 MPa, which has been subjected to quenching and tempering treatment.
- yield strength: over 450 MPa includes a case where the steel has a strength of “X65” grade or higher, which is a strength grade used in the line pipe field.
- the thick high strength seamless steel pipe of the present invention has a U-shaped distribution as shown in FIG. 2 or a M-shaped distribution as shown in FIG.
- the steel pipe has a mold distribution and the hardness of the outermost layer of the pipe is a Vickers hardness HV5 measured at a load of 5 kgf (test force: 49 N) and is 250 HV5 or less.
- the hardness distribution in the entire thickness direction of the steel pipe of the present invention is in accordance with the provisions of JIS Z 2244, using a Vickers hardness tester with a load of 5 kgf (test force: 49 N), and pipe thickness at intervals of 0.5 mm from the surface layer. It shall be obtained by measuring the entire area in the thickness direction.
- the position of the outermost layer of the pipe is the outermost or innermost position of the pipe where the Vickers hardness can be measured with a load of 5 kgf (test force: 49 N).
- the position of the outermost layer of the pipe is 0.
- the position is about 4 to 0.6 mm away. As the hardness decreases, the indentation increases, and the position of the outermost layer of the tube is further inside.
- the thickness distribution in the thickness direction of the “U-type” in the present invention has a low hardness at the tube thickness center, and the hardness increases toward the tube outer surface side and the tube inner surface side. An increasing distribution.
- the “M-type” thickness direction hardness distribution shows the highest hardness at a position where the hardness of the surface layer decreases and enters the thickness direction somewhat from the surface. A distribution whose hardness decreases toward the thickness center.
- HV S The seamless steel tube exhibiting a U-type hardness distribution as shown in FIG. 2, the tube outermost layer hardness (hereinafter, referred to as HV S) is, load: 5 kgf (test force: 49N) was measured by Vickers hardness If the HV5 is 250 HV5 or less, the HIC resistance and SCC resistance defined in NACE TM0284, NACE TM0177, ASME G39, etc. can be satisfied, and the sour resistance is remarkably improved. Tubes outermost layer hardness HV S is, in the case of more than 25HV5 is, NACE TM0284 and, NACE TM0177, at specified test to ASME G39, etc., it often occurs cracking.
- the maximum hardness (hereinafter also referred to as HV MAX ) of the M-type thickness direction hardness distribution satisfies a Vickers hardness HV5 measured at a load of 5 kgf (test force: 49 N) and satisfies 250 HV5 or less. In order to further improve the sour resistance, it is more preferable.
- the above-mentioned thickness direction hardness distribution starts from the outermost layer (the backmost layer) capable of measuring the hardness with a load of 5 kgf (test force 49 N), and shows a U-shaped thickness direction hardness distribution.
- M-type hardness distribution is often exhibited. This is because when the outermost surface layer region is soft, the outermost surface layer capable of measuring the hardness with a large load is located at an inner position far from the outermost surface.
- a steel pipe whose thickness direction thickness distribution measured with a load of 5 kgf (test force 49 N) is classified as U-shaped can measure up to a soft region near the outermost surface when measuring the hardness with a load of less than 5 kgf. This means that it may be classified as M type.
- a preferable composition of the thick-walled high-strength seamless steel pipe of the present invention having the above-described characteristics is as follows.
- the thick-walled high-strength seamless steel pipe of the present invention is, in mass%, C: 0.03-0.15%, Si: 0.02-0.5%, Mn: 0.7-2.5%, P : 0.020% or less, S: 0.003% or less, Al: 0.01 to 0.08%, Ti: 0.005 to 0.05%, N: 0.005% or less, and Ti N is the following formula (1) N ⁇ Ti ⁇ 14/48 ⁇ N + 10 (1) (Here, Ti, N: content of each element (mass ppm)) And has a composition comprising the balance Fe and inevitable impurities.
- C 0.03-0.15%
- C contributes to an increase in steel pipe strength through solid solution strengthening and hardenability improvement, but increases the hardness of the weld heat affected zone (HAZ) and weld metal during circumferential welding of the steel pipe. For this reason, it is desirable to reduce C as much as possible.
- HAZ weld heat affected zone
- 0 is required in order to ensure a desired strength of the base metal.
- 0.03% or more content is required.
- the content exceeds 0.15%, the hardness of the HAZ becomes too high, causing a problem in the sour resistance of the weld. Therefore, C is preferably limited to 0.03 to 0.15%.
- a preferable range is C range which excluded the hypoperitectic region (volume-expansion) and the hypoperitectic region where manufacturability falls. Since the sub-peritectic region changes depending on the components other than C, it cannot be accurately displayed if the component system is not clear, but is generally around C: 0.10 to 0.12% Often become an area of
- Si 0.02 to 0.5% Si contributes as a deoxidizing agent and contributes to increasing the strength of the steel pipe by solid solution strengthening. In order to obtain such an effect, it is necessary to contain 0.02% or more exceeding the impurity level. On the other hand, if the content exceeds 0.5%, the toughness of the welded part and the base metal part is lowered. For this reason, Si is preferably limited to a range of 0.02 to 0.5%.
- Mn 0.7 to 2.5%
- Mn has an action of improving the hardenability and increasing the strength of the seamless steel pipe that is subjected to quenching and tempering treatment. Even in consideration of the composite inclusion of hardenability improving elements other than Mn, in order to ensure the desired steel pipe strength, a content of 0.7% or more is required. On the other hand, if it contains a large amount exceeding 2.5%, the hardness of the surface layer and the base material, and the hardness in HAZ at the time of circumferential welding become too high exceeding 250 HV, and sour resistance decreases. For this reason, Mn is preferably limited to a range of 0.7 to 2.5%. More preferably, it is 0.7 to 1.5%.
- Mn is contained in order to achieve high strength of the pipe as a bainite-based structure (a bainite single phase, or a structure including a bainitic ferrite phase and an acicular ferrite phase).
- the bainite-based structure has a slightly lower hardness as it is quenched than the martensite-based structure.
- the as-quenched hardness is easily affected by the cooling rate. This is because when the cooling rate is fast (specifically, the outermost layer), the hardness is high, and when the cooling rate is slow (specifically, at the center of the wall thickness), it tends to be lower than the outermost layer. Accompanied by. For this reason, in such a component system, the hardness distribution in the thickness direction tends to increase sharply toward the surface layer.
- P 0.020% or less
- P is an element that reduces sour resistance. P segregates at grain boundaries and induces intergranular cracks during hydrogen embrittlement, thereby reducing SSC resistance among the sour resistance. P also reduces toughness. Therefore, in the present invention, it is desirable to reduce P as much as possible, but it is acceptable if it is 0.020% or less. Therefore, P is preferably limited to 0.020% or less. P is desirably reduced as much as possible. However, excessive reduction is accompanied by an increase in steelmaking cost, and therefore, industrially, it is preferably about 0.003% or more.
- S 0.003% or less S is present as an inclusion and lowers sour resistance, particularly HIC resistance, so it is desirable to reduce it as much as possible.
- the material is rolled in the circumferential direction and the longitudinal direction in the piercing and rolling process (peering process in seamipe pipe), so that a steel plate or steel plate is used.
- MnS does not extend significantly in the rolling direction and has a significant adverse effect on the HIC resistance. For this reason, in the present invention, it is not necessary to extremely reduce S, but if it is 0.003% or less, the decrease in HIC resistance is small and is in an acceptable range. Therefore, S is preferably limited to 0.003% or less.
- Al 0.01 to 0.08%
- Al is an element that acts as a deoxidizer, and such an effect is recognized with a content of 0.01% or more.
- inclusions mainly oxides
- Al is preferably limited to a range of 0.01 to 0.08%. In addition, More preferably, it is 0.05% or less.
- Ti 0.005 to 0.05% Ti is contained only for fixing nitrogen N.
- the amount of Ti is adjusted in accordance with the N content so that no Ti other than nitrogen is fixed and TiN is formed. In order to acquire such an effect, Ti needs to contain 0.005% or more.
- Ti content exceeding 0.05% increases TiN content or size, and forms Ti sulfide, carbo-sulfide, and carbide.
- the adverse effect of degrading toughness over TiN is greater. For this reason, Ti is preferably limited to a range of 0.005 to 0.05%.
- N 0.005% or less N combines with Ti to form TiN, but as the amount of TiN increases, the toughness tends to decrease, so N is preferably reduced as much as possible. However, since extreme reduction increases the refining cost, N is preferably limited to 0.005% or less.
- Ti and N are contained in the above-described range, and further, the following formula (1) N ⁇ Ti ⁇ 14/48 ⁇ N + 10 (1) (Here, Ti, N: content of each element (mass ppm)) The content is adjusted so as to satisfy. “Ti (ppm) ⁇ 14/48” corresponds to the amount of Ti used when forming TiN (in most cases, the Ti / N ratio is 1.0 in terms of element ratio) and satisfies the formula (1) As such, it is limited to the range of N to (N + 10) ppm.
- Ti (ppm) ⁇ 14/48 When “Ti (ppm) ⁇ 14/48” is less than the amount of N (ppm), solid nitrogen is present, and bonds with nitride-forming elements such as Al, Alternatively, during tempering, carbon-nitride is formed instead of carbide, and the steel pipe properties (mechanical and / or corrosion properties of serum pipe) are reduced. On the other hand, when “Ti (ppm) ⁇ 14/48” exceeds (N + 10) ppm, there is a certain amount of remaining Ti consumed by TiN, and sulfides and carbon sulfides are formed. , Increasing the risk of degrading toughness. For this reason, the relationship between Ti and N is adjusted to satisfy the expression (1).
- the above-mentioned components are basic components, and in addition to these basic components, as selective elements, Cr: 0.5% or less, Mo: 0.3% or less, Ni: 0.3% or less, Cu: 0.0. 1% or more selected from 3% or less, V: 0.05% or less, Nb: 0.05% or less, and / or Ca: 0.002% or less, if necessary, It can be selected and contained.
- Cr 0.5% or less
- Mo 0.3% or less
- Ni 0.3% or less
- Cu 0.3% or less
- V 0.05% or less
- Nb 0.05% or less
- One or more selected Cr, Mo, Ni, Cu, V, and Nb are all elements that contribute to increasing the strength of the steel pipe, and can be contained as necessary.
- Cr 0.5% or less Cr contributes to increasing the strength of the steel pipe through improving hardenability.
- Cr is preferably limited to 0.5% or less. In addition, More preferably, it is 0.3% or less.
- Mo 0.3% or less Mo, like Cr, contributes to increasing the strength of the steel pipe through improving hardenability. In order to ensure such an effect, it is desirable to contain 0.001% or more which is an inevitable impurity level. However, if it contains more than 0.3%, the hardness becomes too high, so Sex is reduced. In particular, containing a large amount of Mo increases the strength of the welded portion and lowers the sour resistance of the welded portion. For this reason, when it contains, it is preferable to limit Mo to 0.3% or less. In addition, More preferably, it is 0.2% or less.
- Ni 0.3% or less Ni contributes to an increase in the strength of the steel pipe through solid solution strengthening and further improvement in hardenability. In order to secure such an effect, it is desirable to contain 0.01% or more, which is an inevitable impurity level, but if it contains a large amount exceeding 0.3%, the strength becomes too high, sour resistance Decreases. For this reason, when it contains, it is preferable to limit Ni to 0.3% or less. In addition, when 0.05% or more of Cu is contained, Ni is preferably contained by 0.5 ⁇ Cu or more. Thereby, generation
- Cu 0.3% or less Cu contributes to an increase in the strength of the steel pipe through solid solution strengthening and further improvement in hardenability. In order to ensure such an effect, it is desirable to contain 0.01% or more, which is an inevitable impurity level. However, if it contains more than 0.3%, toughness decreases and surface flaws occur frequently. There is a problem of doing. For this reason, when it contains, it is preferable to limit Cu to 0.3% or less. In addition, when 0.05% or more of Cu is contained, it is preferable to contain 0.5 ⁇ Cu or more of Ni. Thereby, generation
- V 0.05% or less V contributes to the improvement of hardenability and increases the strength of the steel pipe by increasing the tempering softening resistance. Such an effect becomes remarkable when the content is 0.002% or more, which is the impurity level or more. On the other hand, if the content exceeds 0.05%, coarse VN and V (CN) are formed, and the possibility of lowering toughness increases. For this reason, when it contains, it is preferable to limit V to 0.05% or less.
- Nb 0.05% or less Nb contributes to an increase in the strength of the steel pipe by precipitation strengthening of Nb precipitates. Moreover, Nb contributes to the refinement
- Ca 0.002% or less
- Ca has a morphology control function for controlling the form of sulfides and oxides to a round shape, and contributes to improvement of HIC resistance.
- the Ca content prevents nozzle clogging during continuous casting. In order to ensure such an effect, it is preferable to contain 0.001% or more.
- the content exceeds 0.002%, the amount of Ca-based inclusions and the amount of precipitates are excessively increased, leading to a decrease in toughness and a decrease in SCC resistance. For this reason, when it contains, it is preferable to limit Ca to 0.002% or less.
- Ca may be additive-free. The balance of the above components is composed of Fe and inevitable impurities.
- the structure of the steel pipe of the present invention has a structure mainly composed of a bainite phase.
- the “structure mainly composed of bainite phase” herein includes a bainitic ferrite phase, an acicular ferrite phase, and a martensite phase in addition to the so-called bainite phase.
- the structure of the steel pipe targeted by the present invention is mainly composed of a bainite phase (area ratio of 50% or more), but includes a bainitic ferrite phase and an acicular ferrite phase, and contains a small amount of martensite phase. There is.
- the martensite phase is a little contained, and since it is difficult to distinguish between ordinary nital corrosion and optical microscopic observation, the present invention includes the martensite phase in the “structure mainly composed of bainite phase”. It was decided. It should be noted that the larger the structure fraction of the structure mainly composed of the bainite phase, the more the area ratio is 50% or more.
- the structure of the steel pipe of the present invention is No. 8 or more, preferably no. It is preferable to be 9 or more.
- the second phase other than the bainite phase may contain some (less than 10% area ratio) ferrite phase.
- the ferrite phase is not generated during the tempering process.
- a material steel pipe having the above composition is prepared.
- the raw steel pipe is heated to the above-described steel pipe raw material (round cast slab, round steel slab, etc.), for example, using Mannesmann type pipe making method, piercing rolling, elongating rolling, etc. Therefore, it is preferable to use a seamless steel pipe having a predetermined size, but the present invention is not limited to this.
- the obtained seamless steel pipe is used as a raw steel pipe, and the raw steel pipe is subjected to quenching treatment and tempering treatment to obtain a product steel pipe having a yield strength exceeding 450 MPa.
- the quenching process is a process of heating and then quenching.
- the heating in the quenching process is preferably a process of holding for 120 seconds or more at a heating temperature not lower than the Ac3 transformation point in an air atmosphere.
- “in the atmosphere” means a case where heat treatment is performed in an atmospheric environment (oxygen concentration of about 20%) instead of flowing a gas having a specific composition as an atmosphere gas in an operating heat treatment furnace.
- the heat treatment can be performed in an atmospheric condition close to the atmospheric gas composition (oxygen concentration of about 20%).
- combustion heat such as CH 4 , C 2 H 8 , CO, etc.
- oxygen is consumed during combustion, so the oxygen concentration in the atmosphere decreases to about 10% or less. Absent.
- the heating temperature for quenching is limited to the Ac3 transformation point or higher, preferably 950 ° C or lower. In addition, Preferably it is 850 degreeC or more and 920 degrees C or less.
- the hardness of the surface layer can be set to the desired 250 HV5 or less. If the holding time is less than 120 seconds, decarburization from the surface is insufficient, and the surface hardness after rapid cooling cannot be made to be a desired 250 HV5 or less.
- the atmosphere when heating in an air atmosphere for quenching treatment, the atmosphere has an oxygen concentration equivalent to the atmosphere (about 20%), or at least oxygen. It is preferable to maintain the atmosphere having a concentration of 5% or more at the above-described heating temperature for 300 seconds or more.
- the holding time is less than 300 seconds, the surface layer is not sufficiently decarburized and often does not reach the M-type thickness direction hardness distribution. Therefore, having a thickness direction hardness distribution of M-type, or to further tubes outermost layer of Vickers hardness HV S is a steel pipe is 250HV5 or less, be 300 seconds or longer in quenching heating temperature preferable.
- the upper limit of the heating and holding time is preferably 5400 seconds or less from the viewpoint of productivity. If the time is longer than 5400 seconds, the heat treatment time becomes longer and the productivity is lowered. For this reason, it is preferable that the holding time of heating is limited to 120 seconds or longer, preferably 300 seconds or longer, preferably 5400 seconds or shorter, more preferably 3600 seconds or shorter.
- heating for quenching is performed by charging in a heating furnace in an air atmosphere and heating.
- heating by an induction heating method in an air atmosphere or an electric resistance heating method may be used.
- the atmosphere during heating is an atmosphere having an oxygen concentration substantially equal to the oxygen concentration in the air.
- the material steel pipe heated under the above conditions is then rapidly cooled.
- the rapid cooling is preferably water cooling in a nucleate boiling state.
- the surface layer that is rapidly cooled by cooling in the nucleate boiling state is normally hardened.
- the M-type thickness direction hardness distribution has a lower hardness and a maximum hardness in the middle.
- the rapid cooling may be a process of immersing in a water bath and performing water cooling in a film boiling state for a predetermined time instead of water cooling in a nucleate boiling state, followed by water cooling in the nucleate boiling state.
- the predetermined time of water cooling in the film boiling state is preferably 5 seconds or more.
- the desired thickness direction hardness distribution (M type) is obtained by applying such rapid cooling (water cooling in the film boiling state and then water cooling in the nucleate boiling state). Adjustment to is easier.
- the raw steel pipe is heated to the Ac3 transformation point or higher, preferably 950 ° C. or lower in a non-oxidizing atmosphere, unlike the heating conditions of the quenching treatment described above. And it is good also as the quenching process which water-cools in a nucleate boiling state, and quenches rapidly. In this case, the holding at the above heating temperature is not particularly required. Since the heating for quenching is non-oxidizing, the decarburization of the surface layer as described above does not occur, and in the product steel pipe, the hardness increases as it approaches the surface, so-called U-shaped thickness direction Hardness distribution. For this reason, it is preferable to delete the area
- the surface layer it is preferable to grind the surface layer to delete in the range of about 0.3 mm or more and 0.7 mm or less in the thickness direction from the surface with high hardness. If the grinding exceeds 0.7 mm, the wall thickness decreases too much and it becomes difficult to ensure the product guarantee wall thickness, but from the viewpoint of sour resistance, the grinding is more preferable. In addition, the grinding effect is saturated by grinding about 1.5 mm on one side.
- the hardness tends to decrease by grinding from the surface, but the hardness distribution often has a steep slope on the surface layer, 0.3 mm by grinding or more measurable tubes outermost layer hardness HV S can be 250HV5 below. Thereby, hardness HV S of the pipe outermost layer which can measure hardness can be adjusted to 250HV5 or less.
- the quenching process is usually performed with the quenching Q once, but the quenching Q may be repeated a plurality of times, for example, a QQ process. By repeatedly performing the quenching process, the crystal grains can be expected to be made finer.
- a tempering process is performed after a quenching process.
- the tempering process is performed in order to reduce the hardness and the like obtained by the quenching process and to adjust to ensure desired strength and toughness.
- the tempering process is preferably a process of heating to a temperature (a tempering temperature) not lower than 550 ° C. and not higher than the Ac1 transformation point and allowing to cool. If the tempering temperature is less than 550 ° C., the temperature is too low to ensure the desired toughness. On the other hand, at a high temperature exceeding the Ac1 transformation point, the two-phase region is heated, so that adjustment to desired characteristics becomes impossible.
- Example 1 Molten steel having the composition of steel A shown in Table 1 was melted in a vacuum furnace to form a small steel ingot (30 kilo steel ingot: bottom 100 mm square, top 150 mm square). These small steel ingots were heated to form hot-rolled sheets with five types of plate thickness so that a test material in the range of 9.5 to 41 mm thickness could be secured with an experimental rolling mill. Next, the front and back surfaces of these hot-rolled plates were ground with a milling machine to obtain hot-rolled plates with little thickness variation between the hot-rolled plates.
- Test materials (100 mm width ⁇ 200 mm length (rolling direction)) were sampled from these hot-rolled sheets, and subjected to quenching and tempering treatment under the conditions shown in Table 2. Quenching was carried out in an inert gas (argon gas) atmosphere at a heating temperature of 890 ° C. for 5 minutes and immediately cooled with water in a nucleate boiling state.
- the water cooling in the “nucleate boiling state” mentioned here is a process in which a material to be cooled (hot rolled plate) is gripped with a jig and shaken up and down and left and right in the water tank to cool in a state where steam is not emitted. . In some cases, the sample was immersed in a water tank, cooled for a certain time in a film boiling state, and then rapidly cooled in a nucleate boiling state. Tempering was performed at 650 ° C. for 5 minutes.
- the quenching and tempering treatment for this hot-rolled sheet simulates the quenching and tempering treatment of steel pipes having various thicknesses. Characteristics and sour resistance were estimated. The sour resistance was comprehensively evaluated by conducting a four-point bending test, an HIC test, and a Method-A test defined by NACE-TM0177. The test method was as follows.
- Thickness direction hardness distribution A specimen for hardness measurement is collected from the obtained test material, and the thickness direction cross section is defined by JIS Z 2241 using a Vickers hardness meter (load: 5 kgf). , Hardness HV5 was measured.
- the measurement interval is 5 points at 0.5 mm intervals in the plate thickness direction from the position of both outermost layers (0.5 mm from the surface) of the test material, and further at 3 mm intervals or 4 mm intervals in the plate thickness center direction to the total plate thickness. Measured over time.
- the hardness at that position can be measured with a load of 5 kgf (test force: 49 N). It was hardness HV S of the outermost layer (tube outermost layer).
- the outermost or innermost position that can be measured with a further load of 5 kgf (test force: 49 N) is the load: 5 kgf (test The position was the outermost layer position measurable with force: 49 N).
- the hardness measurement was performed even if hardened. Then, from the distribution form of the hardness distribution in the thickness direction (thickness direction) obtained, it was determined whether it was close to the U type, M type, or flat type.
- the X80 class is defined as YS: 675 to 550 MPa
- the X70 class is defined as YS: 485 to 605 MPa
- the X65 class is defined as YS: 450 to 570 MPa
- the X60 class is defined as YS: 415 to 565 MPa.
- YS is duplicated in the grade.
- those with YS: 550 MPa or more are classified as X80 class, YS: less than 550 MPa, 485 MPa or more, X70 class, YS: less than 485 MPa, 450 MPa or more, X65 class, YS: less than 450 MPa, 415 MPa or more as X60 class. did.
- a 4-point bending test piece was saturated with Solution A solution (5 mass%) NaCl + 0.5 mass% glacial acetic acid aqueous solution (solution of 5% NaCl and 0.5% CH 3 COOH) with a partial pressure of 0.1 MPa and H 2 S gas.
- the sample was immersed in the test solution for 720 hours. When it did not break after immersion, it was evaluated as ⁇ when the SSC resistance was good, and when the break occurred, it was evaluated as ⁇ .
- the yield strength at the lower limit of the standard serving as a reference for the load stress is 550 MPa for the X80 class, 485 MPa for the X70 class, 450 MPa for the X65 class, and 415 MPa for the X60 class.
- HIC test Based on NACE-TM0284, the HIC test piece was extract
- the SSC resistance at the specimen collection position can be evaluated, and the SOHIC resistance can also be evaluated.
- the results obtained are shown in Table 2.
- the hardness distribution in the thickness direction of the steel sheet (steel pipe) having the composition A is almost uniform in the thickness direction when the thickness (sheet thickness) is thin (plate thickness: 9.5 mm, 15 mm). Although it is a flat type (-type) shown, when the thickness is increased, the hardness distribution in the thickness direction of the U type is shown.
- the thickness distribution in the thickness direction after tempering is the test material No. As shown by 1C, the hardness distribution at the time of quenching is not greatly lost, and the hardness distribution at the time of quenching is substantially maintained.
- the hardness HV5 at the outermost layer position (outermost or innermost position) measurable at a load of 5 kgf (test force: 49 N) is 250 HV5 or less, both HIC resistance and SCC resistance are good. It is.
- the test material No. 1E, No. 1 In 1F the hardness HV5 of the measurable outermost layer position (outermost or innermost position) is higher than 250HV5.
- the test material No. 1E, No. 1 1F is evaluated as “x”.
- test materials 2A and 2C were immersed in a water bath and cooled in a film boiling state for 5 seconds and then cooled in a nucleate boiling state.
- the test material 2B was immersed in a water bath and cooled in a film boiling state for 10 seconds and then nucleated in a boiling state. It was cooled with. That is, the test materials 2A, 2B, and 2C are initially slowly cooled and then rapidly cooled.
- the hardness distribution is greatly influenced by the thickness, it can be seen that if such cooling control is performed together, the desired hardness distribution can be easily adjusted.
- Example 2 Molten steel having a composition from steel B to steel I shown in Table 1 was melted in a vacuum furnace to form a small steel ingot (30-kilo steel ingot: bottom 100 mm square, top 150 mm square). These small steel ingots were heated in an experimental heating furnace and formed into a hot rolled sheet having a thickness of 22 to 30 mm with an experimental rolling mill. For some hot-rolled plates, the front and back surfaces were mechanically ground to remove the surface scale. The obtained hot-rolled sheet was heated in an experimental heat treatment furnace in an air atmosphere (oxygen concentration of about 20% by volume) or in an argon gas (inert gas) atmosphere, and quenched by the conditions shown in Table 3, The tempering process which tempers on the conditions shown in 3 was performed. After tempering, it was allowed to cool.
- air atmosphere oxygen concentration of about 20% by volume
- argon gas in an argon gas
- test material in some hot-rolled sheets, was wrapped in stainless steel foil and heated in the atmosphere. Some hot-rolled plates were heated by energization heating in an air atmosphere (oxygen concentration of about 20% by volume). In some hot-rolled sheets, the quenching process was repeated twice. In some hot-rolled sheets, the front and back surfaces were ground by 0.4 mm or 0.7 mm, respectively, after quenching.
- the cooling in the quenching process was water cooling in a nucleate boiling state (cooling in nuclear boiling region) or a film boiling state (cooling in film boiling region).
- what was heat-processed by wrapping in a stainless steel box was water-cooled after removing the stainless steel foil.
- the water cooling in the “nucleate boiling state” is a process in which a material to be cooled (hot rolled plate) is grasped with a jig, shaken up and down, left and right in a water tank, and cooled in a state where steam is not emitted. .
- the water cooling in the “film boiling state” is a treatment in which a material to be cooled (hot rolled plate) is immersed in a water bath (cooled in a dough) and cooled, that is, cooling in a state where steam rises.
- Test materials were collected from the hot-rolled sheets subjected to the quenching and tempering treatment as described above, and the thickness direction hardness distribution, tensile properties, and sour resistance were estimated in the same manner as in Example 1.
- the sour resistance was evaluated comprehensively by conducting a four-point bending test, an HIC test, and a Method-A test.
- the test method was the same as in Example 1.
- the load stress in the 4-point bending test and Method-A test defined in NACE-TM0177 was (measured YS) ⁇ 0.85.
- the direction of JIS Z 2202 is such that the direction perpendicular to the rolling direction (so-called T-direction as defined in DNS-OS-F101) is the specimen longitudinal direction.
- a V-notch test piece was collected in accordance with the regulations, and a Charpy impact test was performed at a test temperature of ⁇ 40 ° C. in accordance with the regulations of JIS Z 2242 to obtain the absorbed energy V E- 40 (J).
- V E- 40 was 200 J or more was evaluated as “good” as toughness, and the others were evaluated as “x”. Table 4 shows the obtained results.
- the hardness of the outermost layer position measurable at a load of 5 kgf is 250 HV5 or less, and the maximum hardness is 250 HV5 or less, so that the sour resistance is remarkably improved.
- the comparative example out of the scope of the present invention is that the hardness of the outermost layer position measurable at a load of 5 kgf (test force: 49 N) is harder than 250 HV5, or the highest hardness is higher than 250 HV5. The sour resistance is low.
- the surface layer is decarburized by heating in an air atmosphere (oxygen concentration of about 20% by volume), and the outermost layer is removed by scale formation, the hardness distribution is adjusted to M type. In the heating in the atmosphere, the surface layer is not decarburized and scale formation is not observed, so the hardness distribution is adjusted to U shape.
- Example 3 Molten steel having the composition of steel A and steel J to steel M shown in Table 1 is melted in a converter and made into a slab (steel material: wall thickness: 250 mm) by a continuous casting method, and the slab is hot-rolled. A steel piece (steel pipe material) having a round shape (diameter: 150 mm ⁇ or 200 mm ⁇ ) was used. The steel slab was heated, pierced and rolled using a Mannesmann-Piercer mill, made into a hollow material, and further stretched and rolled using a Mannesmann-Mandrel mill or the like to obtain a material steel pipe (seamless steel pipe) having the dimensions shown in Table 3.
- the heating furnace used is for actual operation, surface decarburization occurs when the time to reach the heating temperature is as long as 1 to 2 hours and the holding time is as long as 600 seconds or more, and the hardness distribution is M type.
- the water cooling was nucleate boiling water cooling.
- the tempering process was set as the process which cools, after charging in the heating furnace of an atmospheric atmosphere and hold
- Test pieces were collected from the obtained seamless steel pipes, and subjected to a four-point bending test, an HIC test, and a Method-A test in order to evaluate the hardness test, the tensile test, and the sour resistance.
- the 4-point bending specimen was collected so as to include the inner surface of the steel pipe.
- the test method was the same as in Example 1. The results obtained are shown in Table 6.
- the hardness of the outermost layer position measurable at a load of 5 kgf is 250 HV5 or less, and the maximum hardness is 250 HV5 or less, so that the sour resistance is remarkably improved.
- the hardness of the outermost layer position measurable at a load of 5 kgf is harder than 250 HV5, and sour resistance is reduced.
- Steel pipe No. which is a comparative example. 34, no. No.
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Abstract
Description
(1)焼入焼戻処理を施されてなる、降伏強さ(yield strength):450MPa超えを有する厚肉高強度継目無鋼管であって、管最外側または管最内側で荷重:5kgf(試験力:49N)で測定可能なビッカース硬さ(Vickers hardness)HV5が、250HV5以下であることを特徴とする耐サワー性に優れたラインパイプ用厚肉高強度継目無鋼管。
(2)(1)において、前記厚肉高強度継目無鋼管の板厚方向全域の硬さ分布が、M型を呈することを特徴とするラインパイプ用厚肉高強度継目無鋼管。
(3)(1)において、前記厚肉高強度継目無鋼管の板厚方向全域の硬さ分布が、U型を呈することを特徴とするラインパイプ用厚肉高強度継目無鋼管。
(4)(2)において、前記厚肉高強度継目無鋼管の板厚方向全域の硬さ分布が、前記M型を呈し、かつ最高硬さが荷重:5kgf(試験力:49N)で測定したビッカース硬さHV5で、250HV5以下であることを特徴とするラインパイプ用厚肉高強度継目無鋼管。
(5)(1)~(4)のいずれかにおいて、前記継目無鋼管が、質量%で、C:0.03~0.15%、Si:0.02~0.5%、Mn:0.7~2.5%、P:0.020%以下、S:0.003%以下、Al:0.01~0.08%、Ti:0.005~0.05%、N:0.005%以下を含み、かつTiとNを次(1)式
N ≦ Ti×14/48 ≦ N+10 ‥‥(1)
(ここで、Ti、N:各元素の含有量(質量ppm))
を満足するように含有し、残部Feおよび不可避不純物からなる組成を有することを特徴とするラインパイプ用厚肉高強度継目無鋼管。
(6)(5)において、前記組成に加えてさらに、質量%で、Cr:0.5%以下、Mo:0.3%以下、Ni:0.3%以下、Cu:0.3%以下、V:0.05%以下、Nb:0.05%以下のうちから選ばれた1種または2種以上を含有することを特徴とするラインパイプ用厚肉高強度継目無鋼管。
(7)(5)または(6)において、前記組成に加えてさらに、質量%で、Ca:0.002%以下を含有することを特徴とするラインパイプ用厚肉高強度継目無鋼管。
N≦ Ti×14/48 ≦ N+10 ‥‥(1)
(ここで、Ti、N:各元素の含有量(質量ppm))
を満足するように含有し、残部Feおよび不可避不純物からなる組成を有する継目無鋼管とし、前記焼入処理を、Ac3変態点以上の温度に加熱し、その後に急冷を行う処理とし、該焼入処理後に表層を板厚方向深さで表面から0.3mm以上研削する加工処理を施し、しかる後に前記焼戻処理を行うことを特徴とする耐サワー性に優れたラインパイプ用厚肉高強度継目無鋼管の製造方法。
前記素材鋼管が、質量%で、C:0.03~0.15%、Si:0.02~0.5%、Mn:0.7~2.5%、P:0.020%以下、S:0.003%以下、Al:0.01~0.08%、Ti:0.005~0.05%、N:0.005%以下を含み、かつTiとNを次(1)式
N≦ Ti×14/48 ≦ N+10 ‥‥(1)
(ここで、Ti、N:各元素の含有量(質量ppm))
を満足するように含有し、残部Feおよび不可避不純物からなる組成を有する継目無鋼管とし、前記焼入処理を、加熱とその後に急冷を行う処理とし、前記加熱が、大気雰囲気中でAc3変態点以上の加熱温度に、120s以上保持する処理とし、前記急冷が、核沸騰状態で水冷する処理とすることを特徴とする耐サワー性に優れたラインパイプ用厚肉高強度継目無鋼管の製造方法。
(11)(8)ないし(10)のいずれかにおいて、前記加熱が、加熱炉装入方式、通電加熱方式、または誘導加熱方式のいずれかによる加熱であることを特徴とするラインパイプ用厚肉高強度継目無鋼管の製造方法。
(12)(8)ないし(11)のいずれかにおいて、前記組成に加えてさらに、質量%で、Cr:0.5%以下、Mo:0.3%以下、Ni:0.3%以下、Cu:0.3%以下、V:0.05%以下、Nb:0.05%以下のうちから選ばれた1種または2種以上を含有することを特徴とするラインパイプ用厚肉高強度継目無鋼管の製造方法。
(13)(8)ないし(12)のいずれかにおいて、前記組成に加えてさらに、質量%で、Ca:0.002%以下を含有することを特徴とするラインパイプ用厚肉高強度継目無鋼管の製造方法。
N≦ Ti×14/48 ≦ N+10 ‥‥(1)
(ここで、Ti、N:各元素の含有量(質量ppm))
を満足するように含有し、残部Feおよび不可避不純物からなる組成を有する。
Cは、固溶強化や、焼入れ性向上を介して、鋼管強度の増加に寄与するが、鋼管の周溶接時に、溶接熱影響部(HAZ)や溶接金属部の硬さを増加させる。このため、Cはできるだけ低減することが望ましいが、所望の母材強度を確保するためには、Si、Mn等の焼入れ性向上元素(hardenability−improved elements)の添加効果を考慮しても、0.03%以上の含有を必要とする。一方、0.15%を超える含有は、HAZの硬度が高くなりすぎて、溶接部の耐サワー性に問題が生じる。このようなことから、Cは0.03~0.15%に限定することが好ましい。なお、より好ましくは0.06~0.12%である。また、リールバージ(reel barge)等のように、円周溶接部が巻き・巻き戻し(wind and rewind)を複数回繰り返すような使途向けの場合には、溶接部の硬さ増加をできるだけ低くするという観点から、さらに好ましくは0.06~0.11%である。なお、好ましい範囲は、体積膨張(volume expansion)が大きく製造性が低下する亜包晶域(hypo−peritec region)を外したC範囲である。亜包晶域は、C以外の含有成分にも依存して変化するため、成分系が明確でない場合には正確には表示することができないが、概ねC:0.10~0.12%前後の領域になることが多い。
Siは、脱酸剤(deoxidizing agent)として寄与するとともに、固溶強化(solid solution strengthening)により、鋼管の高強度化に寄与する。このような効果を得るためには、不純物レベルを超える、0.02%以上の含有を必要とする。一方、0.5%を超える多量の含有は、溶接部および母材部の靭性が低下する。このため、Siは0.02~0.5%の範囲に限定することが好ましい。
Mnは、焼入れ性(hardenability)を向上させて、焼入焼戻処理(quenching and tempering treatment)を施す、継目無鋼管を高強度化する作用を有する。Mn以外の焼入れ性向上元素の複合含有を勘案しても、所望の鋼管強度を確保するためには、0.7%以上の含有を必要とする。一方、2.5%を超える多量の含有は、表層や母材の硬さ、円周溶接時のHAZにおける硬さが、250HVを超えて高くなりすぎて、耐サワー性が低下する。このため、Mnは0.7~2.5%の範囲に限定することが好ましい。なお、より好ましくは0.7~1.5%である。
Mnは、鋼管の組織をベイナイト主体の組織(ベイナイト単相、またはベイニティックフェライト相、アシキュラーフェライト相を含んだ組織)として、管の高強度化を達成するために含有させる。しかし、ベイナイト主体の組織は、マルテンサイト主体の組織と比べて、焼入れまま硬さが、若干低めとなるが、焼入れまま硬さが、冷却速度によって影響を受けて、変化しやすくなる。というのは、冷却速度が速い場合(具体的に最表層)には、硬さが高くなり、冷却速度が遅い場合(具体的に肉厚中央)には、最表層に比べて、低くなる傾向を伴う。このため、このような成分系では、肉厚方向の硬さ分布が、表層に向かって急峻に増加する傾向となる。
Pは、耐サワー性を低下させる元素である。Pは、結晶粒界(grain boundary)に偏析して、水素脆化(hydrogen embrittlement)時に粒界割れ(intergranular crack)を誘起し、耐サワー性のうち、耐SSC性を低下させる。また、Pは、靭性をも低下させる。このため、本発明では、Pはできるだけ低減することが望ましいが、0.020%以下であれば許容できる。このようなことから、Pは0.020%以下に限定することが好ましい。Pは、できるだけ低減することが望ましいが、過剰の低減は、製鋼コスト(steelmaking cost)の高騰を伴うため、工業的には、0.003%程度以上とすることが望ましい。
Sは、介在物(inclusion)として存在し、耐サワー性、特に耐HIC性を低下させるため、できるだけ低減することが望ましい。継目無鋼管では、穿孔圧延工程(piercing process in seamless pipe)で素材に円周方向(circumferential direction)と長手方向(longitudinal direction)に伸ばされる圧延が施されるため、厚鋼板(steel plate)や薄鋼板(steel sheet)のように、MnSが圧延方向に長く伸びて、耐HIC性に著しい悪影響を及ぼすことは少ない。このため、本発明ではSを極端に低減する必要はないが、0.003%以下であれば、耐HIC性の低下は少なく、許容できる範囲となる。このようなことから、Sは0.003%以下に限定することが好ましい。
Alは、脱酸剤として作用する元素であり、このような効果は0.01%以上の含有で認められる。一方、0.08%を超える含有は、酸素と結びつき介在物(主として酸化物)がクラスター状(cluster state)に残留し、靭性(toughness)を低下させる。介在物の増加は、表面疵(surface defects)の原因となることもある。このようなことから、Alは0.01~0.08%の範囲に限定することが好ましい。なお、より好ましくは、0.05%以下である。
Tiは、窒素Nを固定するだけのために含有する。窒素を固定しTiNを形成した以外のTiが残留しないように、N含有量に応じてTi量を調整する。このような効果を得るために、Tiは、0.005%以上の含有を必要とする。一方、0.05%を超えるTi含有は、TiN量が増え、または、サイズが大きくなるとともに、Tiの硫化物(sulfide)、炭硫化物(carbo−sulfide)、炭化物(carbide)を形成し、TiN以上に靭性を劣化させる悪影響が大きくなる。このため、Tiは0.005~0.05%の範囲に限定することが好ましい。
Nは、Tiと結合してTiNを形成するが、TiN量が増加すると、靭性が低下する傾向となるため、Nはできるだけ低減することが好ましい。しかし、極端な低減は精錬コスト(refining cost)を高騰させるため、Nは0.005%以下に限定することが好ましい。
N≦ Ti×14/48 ≦ N+10 ‥‥(1)
(ここで、Ti、N:各元素の含有量(質量ppm))
を満足するように調整して含有する。
「Ti(ppm)×14/48」は、TiN(殆どの場合、Ti/N比は、元素比で1.0)を形成する際に使用させるTi量に相当し、(1)式を満足するように、N~(N+10)ppmの範囲に限定する。「Ti(ppm)×14/48」がN(ppm)量未満では、固溶窒素(solute nitrogen)が存在することになり、Al等の窒化物形成元素(nitride−former elements)との結合、もしくは、焼戻時に、炭化物ではなく、炭窒化物(carbo−nitride)を形成し、鋼管特性(mechanical and/or corrosion properties of seamless pipe)が低下する。一方、「Ti(ppm)×14/48」が(N+10)ppmを超えて多くなると、TiNに消費された残りのTiがある一定量存在することになり、硫化物および炭硫化物が形成され、靭性を劣化させる危険性が増す。このため、TiとNの関係は(1)式を満足するように調整することとした。
Cr、Mo、Ni、Cu、V、Nbはいずれも、鋼管の強度増加に寄与する元素であり、必要に応じて含有できる。
Crは、焼入れ性向上を介して、鋼管の強度増加に寄与する。このような効果を確保するためには、不可避的不純物レベルである0.01%以上含有することが望ましいが、0.5%を超える多量の含有は、硬さが高くなりすぎて、耐サワー性、とくに溶接部の耐サワー性を低下させる。このため、含有する場合には、Crは0.5%以下に限定することが好ましい。なお、より好ましくは0.3%以下である。
Moは、Crと同様に、焼入れ性向上を介して、鋼管の強度増加に寄与する。このような効果を確保するためには、不可避的不純物レベルである0.001%以上含有することが望ましいが、0.3%を超える多量の含有は、硬さが高くなりすぎて、耐サワー性が低下する。とくに、多量のMo含有は、溶接部の強度を増加させ、溶接部の耐サワー性を低下させる。このため、含有する場合には、Moは0.3%以下に限定することが好ましい。なお、より好ましくは0.2%以下である。
Niは、固溶強化、さらには焼入れ性向上を介して、鋼管の強度増加に寄与する。このような効果を確保するためには、不可避的不純物レベルである0.01%以上含有することが望ましいが、0.3%を超える多量の含有は、強度が高くなりすぎるため、耐サワー性が低下する。このため、含有する場合には、Niは0.3%以下に限定することが好ましい。なお、Cuを0.05%以上含有する場合に、Niは、0.5×Cu以上含有させることが好ましい。これにより、Cu起因の表面疵、表面欠陥の発生を防止することができる。
Cuは、固溶強化、さらには焼入れ性向上を介して、鋼管の強度増加に寄与する。このような効果を確保するためには、不可避的不純物レベルである0.01%以上含有することが望ましいが、0.3%を超える多量の含有は、靭性が低下するとともに、表面疵が多発するという問題がある。このため、含有する場合には、Cuは0.3%以下に限定することが好ましい。なお、Cuを0.05%以上含有する場合には、Niを0.5×Cu以上含有させることが好ましい。これによりCu起因の表面疵、表面欠陥の発生を防止できる。
Vは、焼入れ性向上に寄与するとともに、焼戻軟化抵抗(tempering softening resistance)を増加させて、鋼管の強度増加に寄与する。このような効果は、不純物レベル以上である0.002%以上の含有で顕著となる。一方、0.05%を超える含有は、粗大なVN、V(CN)が形成され、靭性を低下させる可能性が高くなる。このため、含有する場合には、Vは0.05%以下に限定することが好ましい。
Nbは、Nb析出物の析出強化(precipitation−strengthening)により、鋼管の強度増加に寄与する。また、Nbは、オーステナイト粒の細粒化に寄与し、これにより耐サワー性が向上する。このような効果は、0.005%以上の含有で顕著となる。一方、0.05%を超える含有は、耐SCC性、耐HIC性を低下させる可能性がある。このため、含有する場合には、0.05%以下に限定することが好ましい。
Caは、硫化物、酸化物の形態を丸い形状に制御する形態制御作用(morphology control function)を有し、耐HIC性の向上に寄与する。また、Caの含有は、連鋳時のノズル詰まり(nozzle clogging)を防止する。このような効果を確保するために、0.001%以上含有することが好ましい。一方、0.002%を超える含有は、Ca系介在物量、析出物量が多くなりすぎて、かえって靭性の低下、耐SCC性の低下を招く。このため、含有する場合には、Caは0.002%以下に限定することが好ましい。なお、丸鋳片を使用しない製造方法の場合には、Caは無添加でもよい。
上記した成分の残部は、Feおよび不可避不純物からなる。
なお、ベイナイト相を主とする組織の組織分率は面積率で50%以上と多ければ多いほどよい。なお、本発明鋼管の組織は、粒度番号でNo.8以上、好ましくはNo.9以上、とすることが好ましい。
まず、上記した組成の素材鋼管を準備する。
素材鋼管は、上記した鋼管素材(丸鋳片、丸鋼片等)に、加熱し、例えば、マンネスマン式製管法等を使用して、穿孔圧延(piercing rolling)、延伸圧延(elongation rolling)等により、所定寸法の継目無鋼管とすることが好ましいが、これに限定されることはない。
本発明では、得られた継目無鋼管を素材鋼管とし、該素材鋼管に、焼入処理および焼戻処理を施し、降伏強さ:450MPa超える降伏強さの製品鋼管とする。
焼入処理は、加熱とその後に急冷を行う処理とする。
焼入処理における加熱は、大気雰囲気中でAc3変態点以上の加熱温度に、120秒以上保持する処理とすることが好ましい。
これにより、硬さを測定できる管最表層の硬さHVSを、250HV5以下に調整できる。
以下、さらに実施例に基づいて本発明をさらに説明する。
表1に示す鋼A組成の溶鋼を、真空炉で溶製し、小型鋼塊(30キロ鋼塊:底部100mm角、頂部150mm角)とした。これら小型鋼塊を加熱し、実験圧延機で9.5~41mm厚の範囲の試験材が確保できるように5種の板厚の熱延板とした。ついで、これら熱延板の表面および裏面をフライス盤で研削して、各熱延板間の肉厚ばらつきの少ない熱延板とした。
得られた試験材から、硬さ測定用試験片を採取し、板厚方向断面について、ビッカース硬さ計(荷重:5kgf)を用いて、JIS Z 2241の規定に準拠して、硬さHV5を測定した。測定間隔は、試験材の両最表層(表面から0.5mm)位置から、板厚方向に0.5mm間隔で5点、さらに板厚中央方向に、3mm間隔または4mm間隔で、全板厚に亘って測定した。なお、両最表層における測定(各5点)は、一列状に測定できない場合は、千鳥式(図4参照)に測定した。なお、表面から0.5mmの位置で、荷重:5kgf(試験力:49N)による硬さ測定が可能であれば、その位置の硬さが、荷重:5kgf(試験力:49N)で測定可能な最表層(管最表層)の硬さHVSとした。荷重:5kgf(試験力:49N)による硬さ測定ができない場合には、さらに内側の、荷重:5kgf(試験力:49N)で測定できる、最も外側または最も内側の位置が、荷重:5kgf(試験力:49N)で測定可能な最表層位置とした。なお、板厚24mm材については、焼入れままでも硬さ測定を行った。そして、得られた板厚方向(肉厚方向)の硬さ分布の分布形態から、U型、M型、あるいはフラット型のいずれかに近いか、判定した。
得られた試験材から、ASTM E8/E8M−08の規定に準拠して、引張方向が圧延方向となるように、また、試験片中央が板厚中央に一致するように、丸棒引張試験片(ASTM−1/4片:Specimen3(E8))を採取し、引張試験を実施し、引張特性(降伏強さYS)を求めた。
なお、実測した降状強さYSから、各試験材の強度グレードを決定した。DNV−OS−F101規格では、X80級はYS:675~550MPa、X70級はYS:485~605MPa、X65級はYS:450~570MPa、X60級ではYS:415~565MPaと規定しており、隣接する級でYSが重複している。そこで、本発明では便宜的に、YS:550MPa以上のものはX80級とし、YS:550MPa未満485MPa以上をX70級、YS:485MPa未満450MPa以上をX65級、YS:450MPa未満415MPa以上をX60級とした。
得られた試験材から、ISO−7539−2規格に準拠して、試験片長手方向が圧延方向となるように、最表層を含む4点曲げ試験片(厚さ:5mm×幅10mm×長さ75mm)を採取し、4点曲げ試験を実施し、最表層を含む場合の耐SSC性を評価した。4点曲げ試験片表面に歪ゲージを貼布し、所定の応力(規格下限の降伏強さの85%の応力)が負荷されていることを確認したのち歪ゲージ(strain gauge)を外して、4点曲げ試験片を、SolutionA液(5mass%)NaCl+0.5mass%氷酢酸水溶液)(solution of 5%NaCl and 0.5% CH3COOH)に分圧0.1MPa、H2Sガスを飽和させた試験液中に720時間浸漬した。浸漬後に、破断しない場合には、耐SSC性が良好であるとして○、破断が発生した場合には×として評価した。
なお、負荷応力の基準となる規格下限の降状強さは、X80級では550MPa、X70級では485MPa、X65級では450MPa、X60級では415MPaである。
得られた試験材から、NACE−TM0284に準拠して、HIC試験片を採取し、HIC試験を実施した。試験は、試験片をSolutionA液(5mass%NaCl+0.5mass%氷酢酸水溶液)に分圧0.1MPa、H2Sガスを飽和させた試験液中に96時間浸漬する試験とした。浸漬後、試験片の断面を観察し、CSR、CLR、CTRを求めた。CSRが1%以下、CLRが15%以下、CTRが3%以下である場合を、耐HIC性が良好であるとして○とし、ひとつの値でも基準に満たない場合には×とした。
得られた試験材から、NACE−TM0177に準拠して、板厚中央位置が試験片中心となるように丸棒試験片を採取し、耐SSC性を評価した。試験片を、SolutionA液(5mass%NaCl+0.5mass%氷酢酸水溶液)に分圧0.1MPa、H2Sガスを飽和させた試験液中に、所定の応力(規格下限の降伏強さの85%の応力)を負荷して、浸漬し、720時間経過するまでの破断の有無を調査した。なお、規格下限の降状強さは各強度グレードに応じた(3)4点曲げ試験の項に示した値とした。得られた結果から、720時間経過後に未破断であり、かつ10倍の光学顕微鏡で試験片平行部を観察し亀裂がない場合を、耐SSC性に優れるとして○と評価しそれ以外の場合を×とした。
得られた結果を、表2に示す。
表1に示す鋼B~鋼Iまでの組成を有する溶鋼を、真空炉で溶製し、小型鋼塊(30キロ鋼塊:底部100mm角、頂部150mm角)とした。これら小型鋼塊を実験加熱炉で加熱し、実験圧延機で板厚:22~30mm厚の範囲の熱延板とした。なお、一部の熱延板については、表面および裏面を機械研削して、表面スケールを除去した。
得られた熱延板に実験熱処理炉で、大気雰囲気(酸素濃度約20体積%)中またはアルゴンガス(不活性ガス)雰囲気中で加熱し、表3に示す条件で焼入れする焼入れ処理、および表3に示す条件で焼戻する焼戻処理を行った。焼戻後は、放冷した。
得られた結果を表4に示す。
表1に示す鋼A,鋼J~鋼Mまでの組成を有する溶鋼を、転炉で溶製し、連続鋳造法でスラブ(鋼素材:肉厚:250mm)とし、該スラブを熱間圧延により、丸形状(直径:150mmφ又は200mmφ)の鋼片(鋼管素材)とした。該鋼片を、加熱し、マンネスマン−ピアサミルを用いて穿孔圧延し、中空素材とし、さらに、マンネスマン−マンドレルミル等で延伸圧延し、表3に示す寸法の素材鋼管(継目無鋼管)とした。
得られた結果を表6に示す。
比較例である鋼管No.34、No.37は、焼入れ処理の加熱保持時間が好ましい範囲より短く、荷重:5kgf(試験力:49N)で測定可能な最表層位置の硬さが、250HV5を超えて硬くなっており、表層を含む試験片を用いる4点曲げ試験では、浸漬後、720時間までに、破断が発生して、耐サワー性が低下している。比較例の鋼管No.34,No.37を除き、鋼管No.31,32,33、35,36の靭性を評価したところ、鋼管No.35だけが、判定基準のー40℃でのVノッチシャルピーの吸収エネルギー値である、200Jを下回ったので、この鋼管は比較例とした。Ti、Nの規定式を満たさない例であり、窒素がTiで完全固定されず、別の窒化物等が出来た等して、靭性劣化が起こったと思われる。
Claims (13)
- 焼入焼戻処理を施されてなる、降伏強さ:450MPa超えを有する継目無鋼管であって、管最外側または管最内側で荷重:5kgf(試験力:49N)で測定可能なビッカース硬さHV5が、250HV5以下である継目無鋼管。
- 前記継目無鋼管の板厚方向全域の硬さ分布が、M型を呈することを特徴とする請求項1に記載の継目無鋼管。
- 前記継目無鋼管の板厚方向全域の硬さ分布が、U型を呈することを特徴とする請求項1に記載の継目無鋼管。
- 前記継目無鋼管の板厚方向全域の硬さ分布が、前記M型を呈し、かつ最高硬さが荷重:5kgf(試験力:49N)で測定したビッカース硬さHV5で、250HV5以下であることを特徴とする請求項2に記載の継目無鋼管。
- 前記継目無鋼管が、質量%で、
C :0.03~0.15%、 Si:0.02~0.5%、
Mn:0.7~2.5%、 P :0.020%以下、
S :0.003%以下、 Al:0.01~0.08%、
Ti:0.005~0.05%、 N :0.005%以下
を含み、かつTiとNを下記(1)式を満足するように含有し、残部Feおよび不可避不純物からなる組成を有することを特徴とする請求項1ないし4のいずれかに記載の継目無鋼管。
記
N ≦ Ti×14/48 ≦ N+10 ‥‥(1)
ここで、Ti、N:各元素の含有量(質量ppm) - 前記組成に加えてさらに、質量%で、Cr:0.5%以下、Mo:0.3%以下、Ni:0.3%以下、Cu:0.3%以下、V:0.05%以下、Nb:0.05%以下のうちから選ばれた1種または2種以上を含有することを特徴とする請求項5に記載の継目無鋼管。
- 前記組成に加えてさらに、質量%で、Ca:0.002%以下を含有することを特徴とする請求項5または6に記載の継目無鋼管。
- 素材鋼管に、焼入処理および焼戻処理を施し、降伏強さ:450MPa超えを有する製品鋼管とする継目無鋼管の製造方法であって、
前記素材鋼管を、質量%で、
C :0.03~0.15%、 Si:0.02~0.5%、
Mn:0.7~2.5%、 P :0.020%以下、
S :0.003%以下、 Al:0.01~0.08%、
Ti:0.005~0.05%、 N :0.005%以下
を含み、かつTiとNを下記(1)式を満足するように含有し、残部Feおよび不可避不純物からなる組成を有する継目無鋼管とし、
前記焼入処理を、Ac3変態点以上の温度に加熱し、その後に急冷を行う処理とし、該焼入処理後に表層を板厚方向深さで表面から0.3mm以上研削する加工処理を施し、しかる後に前記焼戻処理を行う継目無鋼管の製造方法。
記
N ≦ Ti×14/48 ≦ N+10 ‥‥(1)
ここで、Ti、N:各元素の含有量(質量ppm) - 素材鋼管に、焼入処理および焼戻処理を施し、降伏強さ:450MPa超えを有する製品鋼管とする継目無鋼管の製造方法であって、
前記素材鋼管が、質量%で、
C :0.03~0.15%、 Si:0.02~0.5%、
Mn:0.7~2.5%、 P :0.020%以下、
S :0.003%以下、 Al:0.01~0.08%、
Ti:0.005~0.05%、 N :0.005%以下
を含み、かつTiとNを下記(1)式を満足するように含有し、残部Feおよび不可避不純物からなる組成を有する継目無鋼管とし、
前記焼入処理を、加熱とその後に急冷を行う処理とし、前記加熱が、大気雰囲気中でAc3変態点以上の加熱温度に、120秒以上保持する処理とし、前記急冷が、核沸騰状態で水冷する処理とする継目無鋼管の製造方法。
記
N ≦ Ti×14/48 ≦ N+10 ‥‥(1)
ここで、Ti、N:各元素の含有量(質量ppm) - 前記急冷が、核沸騰状態で水冷する処理に代えて、膜沸騰状態で水冷した後核沸騰状態で水冷する処理とする継目無鋼管の製造方法。
- 前記加熱が、加熱炉装入方式、通電加熱方式、誘導加熱方式のいずれかによる加熱であることを特徴とする請求項8ないし10のいずれかに記載の継目無鋼管の製造方法。
- 前記組成に加えてさらに、質量%で、Cr:0.5%以下、Mo:0.3%以下、Ni: 0.3%以下、Cu:0.3%以下、V:0.05%以下、Nb:0.05%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8ないし11のいずれかに記載の継目無鋼管の製造方法。
- 前記組成に加えてさらに、質量%で、Ca:0.002%以下を含有する請求項8ないし12のいずれかに記載の継目無鋼管の製造方法。
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JP6047947B2 (ja) | 2016-12-21 |
EP2728030A4 (en) | 2015-09-02 |
BR112013034058A2 (pt) | 2017-02-07 |
NO2728030T3 (ja) | 2018-05-26 |
CN103635600B (zh) | 2016-10-19 |
JP2013032584A (ja) | 2013-02-14 |
EP2728030B1 (en) | 2017-12-27 |
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