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
  • C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
• • 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
  • C21D8/005—Modifying the physical properties by deformation combined with, or followed by, heat treatment 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
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0205—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips 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
  • C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0221—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
  • C21D8/0226—Hot rolling
• • 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
  • C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0247—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
  • C21D8/0263—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment following hot rolling
• • 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
  • 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
  • C22C38/005—Ferrous alloys, e.g. steel alloys containing rare earths, i.e. Sc, Y, Lanthanides
• • 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
  • C22C38/12—Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
• • C—CHEMISTRY; METALLURGY
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/14—Ferrous alloys, e.g. steel alloys containing titanium or zirconium
• • 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
  • C21D2211/002—Bainite

Definitions

• the present invention relates to a thick-walled high-strength hot rolled steel sheet which is preferably used as a raw material for manufacturing a high strength welded steel pipe which is required to possess high toughness when used as a line pipe for transporting crude oil, a natural gas or the like and a manufacturing method thereof, and more particularly to the enhancement of low-temperature toughness and hydrogen induced cracking resistance.
• thick-walled steel sheet means a steel sheet having a sheet thickness of not less than 8.7 mm and not more than 35.4 mm.
• steel sheet is a concept which includes a steel sheet and a steel strip.
• a transport pipe which is used for transporting crude oil or a natural gas which contains hydrogen sulfide is required to be excellent in so-called sour gas resistances such as hydrogen introduced cracking resistance (HIC resistance) or stress corrosion cracking resistance in addition to properties such as high strength and high toughness.
• sour gas resistances such as hydrogen introduced cracking resistance (HIC resistance) or stress corrosion cracking resistance in addition to properties such as high strength and high toughness.
• patent document 1 proposes a method of manufacturing a high strength line-pipe-use steel sheet which possesses excellent hydrogen induced cracking resistance.
• a technique disclosed in patent document 1 is directed to a method of manufacturing a steel sheet for a high-strength electric resistance welded steel pipe of APIX 70 grade or more. That is, patent document 1 describes a method of manufacturing a steel sheet for a high-strength line pipe having excellent hydrogen induced cracking resistance, wherein a slab is heated at a temperature of 1000° C. to 1200° C. and is subjected to hot rolling thus forming a steel sheet, the steel sheet is cooled down such that a surface temperature of the steel sheet becomes a temperature of 500° C.
• patent document 2 proposes a method of manufacturing a high strength steel plate which possesses excellent hydrogen induced cracking resistance.
• a technique disclosed in patent document 2 is directed to a method of manufacturing a steel sheet for a high-strength steel pipe of APIX 60 grade or more. That is, patent document 2 describes a method of manufacturing a high strength steel plate having excellent hydrogen induced cracking resistance, wherein a slab is heated at a temperature of 1000° C. to 1200° C., the slab is subjected to rolling at a reduction rate of 60% or more in an austenite temperature range of 950° C. or below, a steel plate formed by rolling is cooled from (Ar 3 ⁇ 50° C.) or above until a surface temperature of the steel plate becomes 500° C.
• the present invention has been made to overcome the above-mentioned drawbacks, and it aims to provide a thick-walled high-strength hot rolled steel sheet with which a high-strength welded steel pipe of X65 grade or more can be manufactured and possesses excellent hydrogen induced cracking resistance, and a method of manufacturing the thick-walled high-strength hot rolled steel sheet.
• Inventors of the present invention have made studies extensively on various factors which influence surface layer hardness. As a result, the inventors have found that it is possible to stably manufacture a thick-walled high-strength hot rolled steel sheet having tensile strength of 520 MPa or more by which a high strength welded steel pipe of X65 grade or more having low surface layer hardness of 230HV or less can be manufactured in the following manner.
• the steel sheet in manufacturing the hot rolled steel sheet by applying hot rolling consisting of rough rolling and finish rolling to a raw steel material having composition which contains C, Nb, Ti such that C, Nb, Ti satisfy a specific relational formula or in which alloy element quantities are adjusted such that at least one of a carbon equivalent Ceq or Pcm takes a predetermined value or less, the steel sheet is cooled by applying intermittent cooling to the steel sheet after the finish rolling is finished.
• the inventors of the present invention have made further studies based on the above-mentioned finding and have made the present invention.
• a thick-walled high-strength hot rolled steel sheet having a composition which contains by mass % 0.02 to 0.08% C, 1.0% or less Si, 0.50 to 1.85% Mn, 0.03% or less P, 0.005% or less S, 0.1% or less Al, 0.02 to 0.10% Nb, 0.001 to 0.05% Ti, 0.0005% or less B, and Fe and unavoidable impurities as a balance, wherein the steel sheet contains Nb, Ti and C in such a manner that a following formula (1) is satisfied, the steel sheet has the structure formed of a bainitic ferrite phase or a bainite phase, and surface layer hardness is 230HV or less in terms of Vickers hardness.
• the composition optionally further contains by mass % one or two kinds or more selected from a group consisting of 0.5% or less V, 1.0% or less Mo, 1.0% or less Cr, 4.0% or less Ni, and 2.0% or less Cu in addition to the above-mentioned composition.
• composition optionally further contains by mass % one or two kinds or more selected from a group consisting of 0.010% or less Ca, 0.02% or less REM, and 0.003% or less Mg in addition to the above-mentioned composition.
• composition optionally further satisfies at least one of a condition that Ceq defined by a following formula (2) is 0.32% or less and a condition that Pcm defined by a following formula (3) is 0.130% or less.
• a method of manufacturing a thick-walled high-strength hot rolled steel sheet having surface layer hardness of 230HV or less in terms of Vickers hardness and having excellent hydrogen induced cracking resistance is also provided, wherein in manufacturing a hot rolled steel sheet by applying hot rolling consisting of rough rolling and finish rolling to a raw steel material having the composition according to the above-mentioned steel sheet, after the finish rolling is finished, a first cooling step in which the hot rolled steel sheet is cooled by accelerated cooling at an average surface cooling rate of 30° C./s or more until a surface temperature becomes 500° C.
• a second cooling step in which the hot rolled steel sheet is cooled by air cooling for 10s or less after the first cooling step is finished
• a third cooling step in which the hot rolled steel sheet is cooled by accelerated cooling to a temperature which falls within a temperature range from 350° C. or above to a temperature below 600° C. at the center of a sheet-thickness at an average cooling rate of 10° C./s or more at the center of the sheet-thickness are applied to the hot rolled steel sheet, and the hot rolled steel sheet is coiled in a coil shape after the third cooling step is finished.
• the accelerated cooling in the third cooling step is optionally cooling performed at a heat flow rate of 1.5 Gcal/m 2 hr or more in entire surface nuclear boiling.
• the composition optionally further contains by mass % one or two kinds or more selected from a group consisting of 0.5% or less V, 1.0% or less Mo, 1.0% or less Cr, 4.0% or less Ni, and 2.0% or less Cu in addition to the above-mentioned composition.
• composition optionally further contains by mass % one or two kinds or more selected from a group consisting of 0.010% or less Ca, 0.02% or less REM, and 0.003% or less Mg in addition to the above-mentioned composition.
• the composition optionally further satisfies at least one of a condition that Ceq defined by a following formula (2) is 0.32% or less and a condition that Pcm defined by a following formula (3) is 0.13% or less.
• a method of manufacturing a thick-walled high-strength hot rolled steel sheet having tensile strength of 520 MPa or more and a surface layer hardness of 230HV or less in terms of Vickers hardness and having excellent hydrogen induced cracking resistance is provided, wherein in manufacturing a hot rolled steel sheet by applying hot rolling consisting of rough rolling and finish rolling to a raw steel material having the composition according to the above-mentioned steel sheet, after the finish rolling is finished, a first cooling step in which the hot rolled steel sheet is cooled by accelerated cooling at an average cooling rate of 20° C./s or more and less than a martensite formation critical cooling rate on a surface of the hot rolled steel sheet until a surface temperature becomes a temperature not more than an A r3 transformation temperature and not less than an Ms temperature, a second cooling step in which the hot rolled steel sheet is rapidly cooled to a temperature within a temperature range from 350° C.
• a third cooling step in which, after the second cooling step is finished, the hot rolled steel sheet is coiled in a coil shape at a coiling temperature falling within a temperature range from 350° C. or above to a temperature below 600° C. in terms of a temperature at the center of sheet-thickness and, thereafter, a temperature of the hot rolled steel sheet at least at a position of 1 ⁇ 4 sheet-thickness to 3 ⁇ 4 sheet-thickness in a coil thickness direction is held or kept within a temperature range from 350° C. or above to a temperature below 600° C. for 30 min or more are sequentially applied to the hot rolled steel sheet.
• the rapid cooling in the second cooling step is optionally cooling at a heat flow rate of 1.0 Gcal/m 2 hr or more in entire surface nuclear boiling.
• the composition optionally further contains by mass % one or two kinds or more selected from a group consisting of 0.5% or less V, 1.0% or less Mo, 1.0% or less Cr, 4.0% or less Ni, and 2.0% or less Cu in addition to the above-mentioned composition.
• composition optionally further contains by mass % one or two kinds selected from a group consisting of 0.010% or less Ca, 0.02% or less REM, 0.003% or less Mg in addition to the above-mentioned composition.
• composition optionally further satisfies at least one of a condition that Ceq defined by a following formula (2) is 0.32% or less and a condition that Pcm defined by a following formula (3) is 0.13% or less.
• the high-strength hot rolled steel sheet which possesses high strength of tensile strength: 520 MPa or more and low surface hardness of 230HV or less, has a large sheet thickness of 8.7 mm or more, possesses excellent hydrogen induced cracking resistance, and can be preferably used as a raw material for a high strength welded steel pipe can be manufactured in a stable manner whereby the present invention can acquire an outstanding industrial advantageous effect. Further, by using the hot rolled steel sheet manufactured by the present invention as a raw material, the present invention can also acquire an advantageous effect that the high strength welded steel pipe possessing excellent hydrogen induced cracking resistance of X65 grade or more can be manufactured at a low cost and also in a stable manner.
• C is an element which performs the action of increasing strength of steel.
• the hot rolled steel sheet preferably contains 0.02% or more of C for securing desired high strength.
• the content of C exceeds 0.08%, a structural fraction of a secondary phase such as pearlite is increased so that base material toughness and toughness of a welded heat affected zone are deteriorated. Accordingly, the content of C is limited to a value which falls within a range from 0.02 to 0.08%.
• the content of C is preferably limited to a value which falls within a range from 0.03 to 0.05%.
• Si is a deoxidizer and also performs the action of increasing strength of steel through solution strengthening and the enhancement of hardenability. Such an advantageous effect can be acquired when the content of Si is 0.01% or more.
• oxide which contains Si is formed at the time of electric resistance welding so that quality of a welded portion is deteriorated and, at the same time, toughness of a welded heat affected zone is deteriorated. Accordingly, the content of Si is limited to 1.0% or less.
• the content of Si is preferably limited to 0.1 to 0.4%.
• Mn performs the action of enhancing hardenability so that Mn increases strength of the steel sheet through the enhancement of hardenability. Further, Mn forms MnS thus fixing S and hence, the grain boundary segregation of S is prevented whereby cracking of slab (raw steel material) can be suppressed.
• the content of Mn is limited to a value which falls within a range from 0.50 to 1.85%.
• the content of Mn is preferably limited to a value which falls within a range from 0.8 to 1.2%.
• P is contained in steel as an unavoidable impurity, P performs the action of increasing strength of steel.
• the content of P is limited to 0.03% or less.
• the content of P is preferably limited to 0.01% or less.
• S is also contained in steel as an unavoidable impurity in the same manner as P.
• S is contained exceeding 0.005%, cracks occur in slab, and coarse MnS is formed in a hot rolled steel sheet thus deteriorating ductility. Accordingly, the content of S is limited to 0.005% or less.
• the content of S is preferably limited to 0.001% or less.
• Al is an element which acts as a deoxidizes and, to acquire such an advantageous effect, it is desirable to set the content of Al to 0.005% or more, and it is more desirable to set the content of Al to 0.01% or more.
• the content of Al exceeds 0.1%, cleanability of a welded part at the time of electric resistance welding is remarkably deteriorated. Accordingly, the content of Al is limited to 0.1% or less.
• the content of Al is preferably limited to a value which falls within a range from 0.005 to 0.05%.
• Nb is an element which performs the action of suppressing the coarsening and the recrystallization of austenite.
• Nb enables rolling in an austenite un-recrystallization temperature range in hot finish rolling and is finely precipitated as carbonitride so that Nb performs the action of increasing strength of hot rolled steel sheet with the small content without deteriorating weldability.
• the content of Nb exceeds 0.10%, a rolling load during hot finish rolling is increased and hence, there may be a case where hot rolling becomes difficult.
• the content of Nb is limited to a value which falls within a range from 0.02 to 0.10%.
• the content of Nb is preferably limited to a value which falls within a range from 0.03% to 0.07%.
• the content of Nb is more preferably limited to a value which falls within a range from 0.04% to 0.06%.
• Ti performs the action of preventing cracks in slab (raw steel material) by forming nitride thus fixing N, and is also finely precipitated as carbide so that strength of a steel sheet is increased.
• the content of Ti is 0.001% or more, when the content of Ti exceeds 0.05%, a yield point is remarkably elevated due to precipitation strengthening. Accordingly, the content of Ti is limited to a value which falls within a range from 0.001 to 0.05%.
• the content of Ti is preferably limited to a value which falls within a range from 0.005% to 0.03%.
• the hot rolled steel sheet preferably contains Nb, Ti, C which fall within the above-mentioned ranges, and the contents of Nb, Ti, C are adjusted such that the following formula (1) is satisfied.
• Nb, Ti are elements which have strong carbide forming tendency, wherein most of C is turned into carbide when the content of C is low, and the drastic decrease of solid-solution C content in ferrite grains is considered.
• the drastic decrease of solid-solution C content in ferrite grains adversely influences circumferential weldability (girth welding property) of a steel pipe at the time of constructing pipelines.
• the grain growth in a heat affected zone (HAZ) of a girth welded part becomes conspicuous thus giving rise to a possibility that toughness of the heat affected zone of the girth welded part is deteriorated.
• the contents of Nb, Ti, C are preferably adjusted so as to satisfy the formula (1). Due to such adjustment, the solid-solution C content in ferrite grains can be set to 10 ppm or more and hence, the deteriorating of toughness of the heat affected zone of the girth weld portion can be prevented.
• B is an element which has a strong tendency of generating segregation in a grain boundary and contributes to the increase of strength of steel through the enhancement of hardenability. This advantageous effect can be acquired when the content of B is 0.0001% or more. However, toughness of steel is deteriorated when the content of B exceeds 0.0005%. Accordingly, the content of B is limited to 0.0005% or less.
• the hot rolled steel sheet may selectively contain one or two kinds or more selected from a group consisting of 0.5% or less V, 1.0% or less Mo, 1.0% or less Cr, 4.0% or less Ni and 2.0% or less Cu and/or one or two kinds selected from a group consisting of 0.010% or less Ca, 0.02% or less REM and 0.003% or less Mg if necessary.
• All of V, Mo, Cr, Ni and Cu are elements which enhance hardenability and increase strength of the steel sheet, and the hot rolled steel sheet may contain one or two kinds or more selected from these elements when necessary.
• V is an element which performs the action of increasing strength of a steel sheet through the enhancement of hardenability and the formation of carbonitride. Such an advantageous effect becomes outstanding when the content of V is 0.01% or more. On the other hand, when the content of V exceeds 0.5%, the weldability is deteriorated. Accordingly, the content of V is preferably limited to 0.5% or less. The content of V is more preferably limited to 0.08% or less.
• Mo is an element which performs the action of increasing strength of a steel sheet through the enhancement of hardenability and the formation of carbonitride. Such an advantageous effect becomes outstanding when the content of Mo is 0.01% or more. On the other hand, when the content of Mo exceeds 1.0%, the weldability is deteriorated. Accordingly, the content of Mo is preferably limited to 1.0% or less. The content of Mo is more preferably limited to a value which falls within a range from 0.05 to 0.35%.
• Cr is an element which performs the action of increasing strength of a steel sheet through the enhancement of hardenability. Such an advantageous effect becomes outstanding when the content of Cr is 0.01% or more. On the other hand, when the content of Cr exceeds 1.0%, there arises a tendency that a welding defect frequently occurs at the time of electric resistance welding. Accordingly, the content of Cr is preferably limited to 1.0% or less. The content of Cr is more preferably limited to less than 0.30%.
• Ni is an element which performs the action of increasing strength of steel through the enhancement of hardenability and also performs the action of enhancing toughness of a steel sheet.
• the content of Ni is preferably set to 0.01% or more.
• the advantageous effect is saturated so that an advantageous effect corresponding to the content is not expected whereby the content of Ni exceeding 4.0% is economically disadvantageous.
• the content of Ni is preferably limited to 4.0% or less.
• the content of Ni is more preferably limited to a value which falls within a range from 0.10 to 1.0%.
• Cu is an element which performs the action of increasing strength of a steel sheet through the enhancement of hardenability and solution strengthening or precipitation strengthening.
• the content of Cu is desirably set to 0.01% or more.
• the content of Cu is preferably limited to 2.0% or less.
• the content of Cu is more preferably limited to a value which falls within a range from 0.10 to 1.0%.
• All of Ca, REM and Mg are elements which contribute to a shape control of sulfide for forming spread coarse sulfide into spherical sulfide, and the composition can selectively contain these elements when necessary.
• the composition contains 0.001% or more of Ca, 0.001% or more of REM.
• the content of Ca exceeds 0.010% or the content of REM exceeds 0.02%, cleanliness of the steel sheet is deteriorated. Accordingly, it is desirable to limit the content of Ca to 0.010% or less and the content of REM to 0.02% or less.
• composition contains Ca within the above-mentioned range, and the content of Ca is adjusted such that ACR which is defined by the following formula satisfies 1.0 to 4.0 in terms of contents of O and S.
• Mg is, in the same manner as Ca or the like, an element which forms sulfide or oxide, suppresses the formation of coarse sulfide MnS, and contributes to a shape control of sulfide.
• the composition may contain Mg when necessary. Such advantageous effects can be acquired when the content of Mg is 0.0005% or more. However, when the content of Mg exceeds 0.003%, clusters of Mg oxide or Mg sulfide are formed thus deteriorating toughness of the steel sheet. Accordingly, when the composition contains Mg, it is preferable to limit the content of Mg to 0.003% or less.
• the composition of the hot rolled steel sheet contains the above-mentioned components within the above-mentioned ranges respectively, and the composition is adjusted such that Ceq defined by a following formula (2) satisfies 0.32% or less, or Pcm defined by a following formula (3) satisfies 0.13% or less.
• the balance other than the above-mentioned components is constituted of Fe and unavoidable impurities.
• the steel sheet is allowed to contain 0.005% or less O, 0.008% or less N, and 0.005% or less Sn.
• O forms various oxides in steel and deteriorates hot-rolling workability, corrosion resistance, toughness and the like. Accordingly, it is desirable to reduce the content of O as much as possible. However, since the extreme reduction of O brings about the sharp rise of a refining cost, the steel sheet is allowed to contain up to 0.005% O.
• N is an element which is unavoidably contained in steel
• the excessive content of N frequently causes cracks at the time of casting a slab. Accordingly, it is desirable to reduce the content of N as much as possible.
• the steel sheet is allowed to contain up to 0.008% N.
• Sn is an element which is mixed into the steel sheet from the scrap used as a steel-making raw material and is unavoidably contained in steel.
• Sn is an element which is liable to be segregated in a grain boundary or the like and hence, when the content of Sn becomes large, grain boundary strength is deteriorated thus deteriorating toughness.
• the steel sheet is allowed to contain up to 0.005% Sn.
• molten steel having the above-mentioned composition is produced by a usual melting method such as a converter, and molten metal is cast into the raw steel material such as slab by a usual casting method such as a continuous casting method.
• a usual melting method such as a converter
• molten metal is cast into the raw steel material such as slab by a usual casting method such as a continuous casting method.
• the present invention is not limited to such a method.
• the raw steel material having the above-mentioned composition is heated and is subjected to hot rolling thus forming a hot rolled steel sheet (steel strip).
• molten steel having the above-mentioned composition is produced by a usual melting method such as a converter, and molten metal is cast into the raw steel material such as slab by a usual casting method such as a continuous casting method.
• a usual melting method such as a converter
• molten metal is cast into the raw steel material such as slab by a usual casting method such as a continuous casting method.
• the present invention is not limited to such a method.
• the hot rolling is constituted of rough rolling which turns the raw steel material (slab) into a sheet bar by heating, and finish rolling which turns the sheet bar into a hot rolled steel sheet.
• heating temperature of a raw steel material is not necessarily limited provided that the raw steel material (slab) can be rolled into a hot rolled steel sheet
• the heating temperature is preferably set to a temperature which falls within a range from 1000 to 1300° C.
• the heating temperature is below 1000° C.
• the deformation resistance is high so that a rolling load is increased whereby a load applied to a rolling mill becomes excessively large.
• the heating temperature in hot rolling is preferably set to a temperature which falls within a range from 1000 to 1300° C.
• the heating temperature is more preferably set to a temperature which falls within a range from 1050 to 1250° C.
• a sheet bar is formed by applying rough rolling to the heated raw steel material (slab). Conditions for rough rolling are not necessarily limited provided that the sheet bar of desired size and shape can be obtained.
• Finish rolling is further applied to the obtained sheet bar thus forming a hot rolled steel sheet.
• finish rolling completion temperature is preferably set to (A C3 ⁇ 50° C.) or less and 800° C. or less, and a total rolling reduction rate (%) in a temperature range of 1000° C. or below is preferably set to 60% or more. This is because when the finish rolling completion temperature falls outside the above-mentioned finish rolling completion temperature range or when the total rolling reduction rate in the temperature range of 1000° C. or below is less than 60%, fine structure cannot be obtained and hence, toughness is deteriorated.
• the hot rolled steel sheet has the structure formed of a bainitic ferrite phase or bainite phase, and surface layer hardness of the steel sheet is 230HV or less in terms of Vickers hardness.
• the present invention provides, as a basic step, the method of manufacturing a thick-walled high-strength hot rolled steel sheet having a surface layer hardness of 230HV or less in Vickers hardness, wherein the cooling step which is performed after the finish rolling is constituted of the first cooling step in which the steel sheet is cooled by accelerated cooling immediately after completion of the finish rolling at the average surface cooling rate equal to or more than predetermined cooling rate such that the precipitation of polygonal ferrite on the surface of the steel sheet is prevented until the surface temperature becomes a temperature equal to or below the A r3 transformation temperature, and the second cooling step in which, after the first cooling step is finished, the steel sheet is cooled by accelerated cooling at the average cooling rate at the center of the sheet thickness to the temperature within the temperature range from 350° C.
• a step of air cooling is performed between the first cooling step and the second cooling step or a step of holding or keeping the steel strip within a temperature range from 350° C. or above to a temperature below 600° C. for 30 minutes or more is performed after coiling.
• the hot rolled steel sheet after being subjected to finish rolling, is subjected to the first cooling step and the second cooling step subsequently, is subjected to the third cooling step thereafter, and is coiled in a coil shape after completion of the third cooling step.
• the hot rolled steel sheet is subjected to accelerated cooling at an average surface cooling rate of 30° C./s or more until the surface temperature becomes 500° C. or below.
• “immediately after the finish rolling” means that cooling is started within 10s after the completion of the finish rolling.
• a surface temperature control is performed in the accelerated cooling in the first cooling step.
• the average surface cooling rate is less than 30° C./s, polygonal ferrite precipitates so that the hot rolled steel sheet cannot achieve the desired enhancement of strength and the desired enhancement of toughness.
• the preferred average surface cooling rate is 100 to 300° C./s.
• a cooling stop temperature in the acceleration cooing is set to a temperature equal to or below 500° C. in terms of the surface temperature. When the cooling stop temperature exceeds 500° C., there is a possibility that transformation on a surface layer is not completed so that the surface layer is transformed into a low-temperature transformation product material in the succeeding cooling step whereby it is no more possible to expect lowering of hardness of the surface layer.
• air cooling is performed for 10s or less after completion of the first cooling step.
• the surface layer recovers heat due to heat which a center portion of the hot rolled steel sheet possesses and hence, the surface layer is tempered whereby lowering of hardness of the surface layer is accelerated. Further, air cooling also brings about an advantageous effect that the succeeding cooling of the hot rolled steel sheet at the center in the sheet thickness direction is enhanced. Even when the air cooling time is prolonged exceeding 10s, the above-mentioned advantageous effect is saturated, and productivity is lowered. Accordingly, air cooling time is limited to a value within 10s. From a viewpoint of enhancing productivity, the air cooling time is preferably set to 7s or less. Further, to acquire a tempering effect of the surface layer by recuperation, air cooling time is preferably set to is or more.
• the hot rolled steel sheet is subjected to accelerated cooling at an average cooling rate of 10° C./s or more at the center of the sheet thickness until the temperature at the center of the sheet thickness becomes a temperature in a temperature range from 350° C. or above to a temperature below 600° C.
• a sheet thickness center temperature control is performed in the accelerated cooling in the third cooling step.
• the average cooling rate at the center of the sheet thickness is less than 10° C./s, polygonal ferrite or pearlite is liable to precipitate so that the hot rolled steel sheet cannot acquire the desired enhancement of strength and the desired enhancement of toughness.
• an upper limit of the average cooling rate at the center of the sheet thickness is decided depending on performance of a cooling device in service, it is desirable to set the upper limit of the average cooling rate to 100° C./s or less which does not bring about deterioration of a shape of the steel sheet such as a warp.
• the preferred average cooling rate at the center in the sheet thickness is 25° C./s or more.
• Such cooling can be achieved by cooling (cooling with water) the hot rolled steel sheet by entire surface nuclear boiling at a heat flow rate of 1.5 Gcal/m 2 hr or more.
• the above-mentioned accelerated cooling is performed until the temperature at the center of sheet thickness becomes a temperature (cooling stop temperature) within a temperature range from 350° C. or above to a temperature below 600° C.
• the cooling stop temperature falls outside this range, after winding the hot rolled steel sheet in a coil shape after accelerated cooling, the hot rolled steel sheet cannot be held within a predetermined temperature range for a predetermined time or more and hence, the hot rolled steel sheet cannot secure desired high strength and desired high toughness.
• the hot rolled steel sheet After being subjected to the third cooling step, the hot rolled steel sheet is coiled in a coil shape at a coiling temperature range from 350° C. or above to a temperature below 600° C.
• the hot rolled steel sheet can be held or kept within the temperature range from 350° C. or above to a temperature below 600° C. for 30 min or more and hence, the enhancement of precipitation is accelerated in the inside of the sheet whereby the hot rolled steel sheet can secure desired high strength and desired high toughness, while hardness of the hot rolled steel sheet at the surface of the hot rolled steel sheet can be lowered due to self annealing.
• the hot rolled steel sheet is subjected to the first cooling step, the second cooling step and the third cooling step sequentially.
• the hot rolled steel sheet is subjected to accelerated cooling until the surface temperature of the hot rolled steel sheet becomes a temperature not more than A r3 transformation temperature and a martensite transformation temperature or more at an average cooling rate of not less than 20° C./s and less than a critical cooling rate of martensite formation.
• “immediately after the completion of the finish rolling” means that cooling is started within 10s after completion of the finish rolling.
• a surface temperature control is performed in the accelerated cooling in the first cooling step.
• the average cooling rate of the surface of the hot rolled steel sheet is less than 20 C.°/s, polygonal ferrite precipitates so that the hot rolled steel sheet cannot achieve the desired enhancement of strength and the desired enhancement of toughness.
• the preferred surface average cooling rate is 50 to 100° C./s.
• the cooling stop temperature in the accelerated cooling is set to an A r3 transformation temperature or below and above a martensite transformation temperature in terms of a surface temperature.
• the cooling stop temperature exceeds the A r3 transformation temperature, there exists a possibility that the transformation in a surface layer region is not completed, and the surface layer is transformed into a low-temperature transformed product in the succeeding cooling step whereby it is no more possible to expect the lowering of hardness of the surface layer.
• the hot rolled steel sheet is rapidly cooled until the hot rolled steel sheet at the center of sheet thickness becomes a temperature within a temperature range from 350° C. or above to a temperature below 600° C. It is preferable to set the cooling rate in the rapid cooling to 10° C./s or more in terms of the average cooling rate at the sheet thickness center position.
• the average cooling rate at the sheet thickness center position is less than 10° C./s, pearlite is liable to precipitate and hence, the hot rolled steel sheet cannot achieve the desired enhancement of strength and the desired enhancement of toughness.
• an upper limit of the average cooling rate at the center of sheet thickness is decided depending on performance of a cooling device in service, it is desirable to set the upper limit of the average cooling rate to 300° C./s or less which does not bring about deterioration of a shape of the steel sheet such as a warp.
• the preferred average cooling rate at the sheet thickness center position is 25° C./s or more.
• Such cooling can be achieved by cooling (cooling with water) the hot rolled steel sheet by entire surface nuclear boiling at a heat flow rate of 1.0 Gcal/m 2 hr or more.
• the temperature and the cooling rate at the sheet thickness center position are obtained by calculation based on the sheet thickness, the surface temperature and the heat flow rate.
• the above-mentioned rapid cooling is performed until the temperature at the center of the sheet thickness becomes a temperature (cooling stop temperature) of 350° C. or above and below 600° C.
• a temperature cooling stop temperature
• the succeeding normal coiling of the hot rolled steel sheet becomes impossible.
• the coiling temperature is 600° C. or more, a grain size becomes coarse so that the hot rolled steel sheet cannot secure high strength and high toughness.
• the hot rolled steel sheet After being subjected to the second cooling step, the hot rolled steel sheet is coiled in a coil shape after the coiling temperature is adjusted to a temperature of 350° C. or above and below 600° C. in terms of a sheet thickness center temperature, and is subjected to the third cooling step where the hot rolled steel sheet at a position of 1 ⁇ 4 sheet-thickness to 3 ⁇ 4 sheet-thickness in the coil thickness direction is held or kept within a temperature range from 350° C. or above to a temperature below 600° C. for 30 min or more.
• the coiling temperature is set to the temperature which falls within the range from 350° C. or more to a temperature below 600° C. in terms of the sheet thickness center temperature.
• the coiling temperature is preferably set to 450 to 550° C.
• the hot rolled steel sheet coiled in a coil shape is subjected to cooling where the hot rolled steel sheet at least at the position of 1 ⁇ 4 sheet thickness to 3 ⁇ 4 sheet thickness in the thickness direction of the coil is held or kept within the temperature range from 350° C. or above to a temperature below 600° C. for 30 min or more.
• the hot rolled steel sheet at the position of 1 ⁇ 4 sheet thickness to 3 ⁇ 4 sheet thickness in the coil thickness direction is held or kept within the temperature range from 350° C. or above to a temperature below 600° C.
• the precipitation is enhanced in the inside of the steel sheet so that the steel sheet can acquire the high strength, while hardness of the steel sheet is lowered in the surface layer of the steel sheet due to self annealing. Accordingly, the hot rolled steel sheet can acquire both the desired high strength and the desired low surface hardness.
• the above-mentioned hot rolled steel sheet acquired by the manufacturing method of embodiments of the present invention is the thick-walled high-strength hot rolled steel sheet having excellent hydrogen induced cracking resistance which has the above-mentioned composition, has the single-phase structure (here, single phase structure meaning the structure where 98% or more of the structure is occupied by one phase) which is constituted of a bainitic ferrite phase or a bainite phase in the inside of the sheet, and has high strength of tensile strength: 520 MPa or more, and low surface layer hardness where hardness of the surface layer is 230HV or less.
• “bainitic ferrite phase” also includes acicular ferrite, acicular ferrite.
• Surface layer means a region within 1 mm from the surface of the steel sheet in the sheet thickness direction.
• Raw steel material (slab) s having the compositions shown in Tables 1 and 2 are subjected to hot rolling under hot rolling conditions shown in Tables 3 and 4. After hot rolling is completed, the hot rolled steel sheets are cooled under cooling conditions shown in Tables 3 and 4, and are coiled in a coil shape at coiling temperatures shown in Tables 3 and 4, and are turned into hot rolled steel sheets (steel strips) having sheet thicknesses shown in Tables 3 and 4.
• Specimens are sampled from the obtained hot rolled steel sheet, and the observation of structure, a hardness test, a tensile test, an impact resistance test, circumferential weldability test, and a hydrogen induced cracking test are carried out with respect to these specimens, and surface hardness, tensile property, toughness, circumferential weldability and hydrogen induced cracking resistance are evaluated. The following test methods are used.
• Structure-observation-use specimens are sampled from the obtained hot rolled steel sheet, cross-sections of the specimens in the rolling direction are polished and etched. The cross section are observed for each specimen with ten visual fields or more at respective positions consisting of a surface layer and a sheet-thickness center position using an optical microscope (magnification: 1000 times), and a kind of the structure is identified and a structural fraction (volume %) are measured.
• Hardness-measurement-use specimens are sampled from the obtained hot rolled steel sheet, a cross-section of the specimen in the rolling direction is polished. Hardness at positions 0.5 mm and 1 mm away from a surface of the specimen in the sheet thickness direction is measured at five points for each position. Arithmetic average values are obtained by calculating the obtained measured values and a higher value is set as surface layer hardness of the hot rolled steel sheet. Here, measurement of hardness is performed using a Vickers hardness meter with a testing force 0.5 kgf.
• a tensile test is carried out with respect to the obtained hot rolled steel sheet such that the longitudinal direction of the specimen is aligned with the direction orthogonal to the rolling direction (C direction) in accordance with provisions of API-5L at a room temperature thus obtaining yield strength YS and tensile strength TS.
• V notch specimens are sampled from a sheet thickness center portion of the obtained hot rolled steel sheet such that the longitudinal direction of the specimen is aligned with the direction orthogonal to the rolling direction (C direction), and a Charpy impact test is carried out in accordance with provisions of JIS Z 2242 thus obtaining absorbed energy (J) at a test temperature of ⁇ 80° C.
• the number of specimens is three and an arithmetic average of the obtained absorbed energy values is obtained, and the arithmetic average is set as an absorbed energy value E ⁇ 80 (J) of the steel sheet.
• the circumferential weldability is evaluated using a y-type weld cracking test. Test plates are sampled from the obtained hot rolled steel sheet, test welding is performed at a room temperature in accordance with the provisions of JIS Z 3158, and the presence or the non-presence of the occurrence of cracks is investigated. The circumferential weldability is evaluated by giving “X:bad” when cracks occur and “ o : good” when no cracks occur.
• HIC specimens (size: 100 mm ⁇ 20 mm) are sampled from the obtained hot rolled steel sheet such that the longitudinal direction of the specimen is aligned with the rolling direction of the steel sheet, and the hydrogen induced cracking resistance is evaluated in accordance with the provisions of TM 0284 of NACE (National Association of Corrosion Engineers).
• a prescribed A solution is used as a test liquid. After immersing the specimens into the test liquid, CLR (%) is measured. It is determined that no hydrogen induced cracking occurs so that hydrogen induced cracking resistance is favorable when CLR is 0%. The presence or the non-presence of the occurrence of blisters is also investigated.
• All examples of the present invention turned out to be high-strength hot rolled steel sheets having excellent hydrogen induced cracking resistance, wherein the hot rolled steel sheet has high strength of tensile strength: 520 MPa or more and low surface layer hardness of 230HV or less, and has a large sheet-thickness of 8.7 mm or more.
• comparison examples which do not fall within the scope of the present invention cannot secure desired properties necessary as a raw material for a high-strength electric-resistance welded steel pipe since the comparison examples cannot secure desired high strength, the comparison examples cannot acquire desired low surface layer hardness, the low temperature toughness is deteriorated, or the circumferential weldability is deteriorated, or hydrogen induced cracking resistance is deteriorated.
• Raw steel materials having the compositions shown in Tables 7 and 8 are subjected to hot rolling under hot rolling conditions shown in Tables 9 and 10. After hot rolling is completed, the hot rolled steel sheets are cooled under cooling conditions shown in Tables 9 and 10, and are coiled in a coil shape at coiling temperatures shown in Tables 9 and 10, and further, the hot rolled steel sheets are cooled under cooling conditions shown in Tables 9 and 10, are turned into hot rolled steel sheets (steel strips) having sheet thicknesses shown in Tables 9 and 10.
• Specimens are sampled from the obtained hot rolled steel sheet, and the observation of structure, a hardness test, a tensile test, an impact resistance test, a circumferential weldability test, and a hydrogen induced cracking test are carried out with respect to these specimens, and a surface hardness, a tensile property, a toughness, a circumferential weldability and a hydrogen induced cracking resistance are evaluated. The following test methods are used.
• Structure-observation-use specimens are sampled from the obtained hot rolled steel sheet, cross-sections of the specimens in the rolling direction are polished and etched.
• the cross section are observed for each specimen with ten visual fields or more at respective positions consisting of a surface layer and a sheet-thickness center position using an optical microscope (magnification: 1000 times), and a kind of the structure is identified and a structural fraction (volume %) are measured.
• Hardness-measurement-use specimens are sampled from the obtained hot rolled steel sheet, a cross-section of the specimen in the rolling direction is polished. Hardness at positions 0.5 mm and 1.0 mm away from a surface of the specimen in the sheet thickness direction is measured at five points or more for each position. Arithmetic average values are obtained by calculating the obtained measured values as surface layer hardness of the hot rolled steel sheet. Here, measurement of hardness is performed using a Vickers hardness meter with a testing force 0.3 kgf (2.9N).
• a tensile test is carried out with respect to the obtained hot rolled steel sheet such that the longitudinal direction of the specimen is aligned with the direction orthogonal to the rolling direction (C direction) in accordance with provisions of API-5L at a room temperature thus obtaining yield strength YS and tensile strength TS.
• V notch specimens are sampled from a sheet thickness center portion of the obtained hot rolled steel sheet such that the longitudinal direction of the specimen is aligned with the direction orthogonal to the rolling direction (C direction), and a Charpy impact test is carried out in accordance with provisions of JIS Z 2242 thus obtaining absorbed energy (J) at a test temperature of ⁇ 80° C.
• the number of specimens is three and an arithmetic average of the obtained absorbed energy values is obtained, and the arithmetic average is set as an absorbed energy value vE ⁇ 80 (J) of the steel sheet.
• the circumferential weldability is evaluated using a y-type weld cracking test. Test plates are sampled from the obtained hot rolled steel sheet, test welding is performed at a room temperature in accordance with the provisions of JIS Z 3158, and the presence or the non-presence of the occurrence of cracks is investigated. The circumferential weldability is evaluated by giving “X:bad” when cracks occur and “ o : good” when no cracks occur.
• HIC specimens (size: 100 mm ⁇ 20 mm) are sampled from the obtained hot rolled steel sheet such that the longitudinal direction of the specimen is aligned with the rolling direction of the steel sheet, and the hydrogen induced cracking resistance is evaluated in accordance with the provisions of TM 0284 of NACE.
• a prescribed A solution is used as a test liquid. After immersing the specimens into the test liquid, CLR (%) is measured. It is determined that no hydrogen induced cracking occurs so that hydrogen induced cracking resistance is favorable when CLR is 0%. The presence or the non-presence of the occurrence of blisters is also investigated.
• All examples of the present invention are turned out to be high-strength hot rolled steel sheets having excellent hydrogen induced cracking resistance, wherein the hot rolled steel sheet has high strength of tensile strength: 520 MPa or more and low surface layer hardness of 2301HV or less, possesses excellent circumferential weldability, and has a large sheet-thickness of 8.7 mm or more.
• comparison examples which do not fall within the scope of the present invention cannot secure desired properties necessary as a raw material for a high-strength electric-resistance welded steel pipe possessing excellent hydrogen induced cracking resistance of X65 grade or more since the comparison examples cannot secure desired high strength, the comparison examples cannot acquire desired low surface layer hardness, the low temperature toughness is deteriorated, or the circumferential weldability is deteriorated, or hydrogen induced cracking resistance is deteriorated.
• Ca REM, Mg of formula (1)* ACR** Ceq*** Pcm**** O Ca: 0.0022 1.221 2.816 0.394 0.160 P Ca: 0.0019 1.438 0.232 0.404 0.170 Q Ca: 0.0022 0.505 2.402 0.293 0.159 R Ca: 0.0021 0.717 2.932 0.216 0.134 S Ca: 0.0020 1.512 2.355 0.218 0.104 T Ca: 0.0023 0.667 3.546 0.214 0.111 U Ca: 0.0019 1.823 3.586 0.213 0.105 V Ca: 0.0019 1.823 3.586 0.213 0.105 W Ca: 0.0019 1.823 0.192 0.213 0.105 X Ca: 0.0021 0.350 0.610 0.292 0.139 Y — 0.837 ⁇ 0.936 0.225 0.099 Z Ca: 0.0020 0.854 1.787 0.086 0.056 AA Mg: 0.0019 0.841 ⁇ 0.490 0.211 0.103 AB Ca: 0.0014, 1.800 1.191 0.290 0.
• Ca, REM, Mg of formula (1)* ACR** Ceq*** Pcm**** A Ca: 0.0018 0.714 2.702 0.296 0.135 B Ca: 0.0020 1.674 2.021 0.278 0.110 C Ca: 0.0022 0.500 2.327 0.299 0.138 D Ca: 0.0021 0.888 1.773 0.135 0.076 E Ca: 0.0017 0.683 2.518 0.284 0.128 F Ca: 0.0019 0.833 3.586 0.215 0.126 G Ca: 0.0019 0.897 2.290 0.202 0.095 H Ca: 0.0018 0.250 2.524 0.205 0.096 I Ca: 0.0018 1.009 2.110 0.233 0.116 J Ca: 0.0111 0.767 12.847 0.211 0.101 K Ca: 0.0020 0.792 2.152 0.226 0.108 L Ca: 0.0021 1.036 2.200 0.210 0.099 M REM: 0.0031 1.073 4.846 0.211 0.099 *left side value of formula (1) (Ti + Nb/2)/C **A

Landscapes

• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Mechanical Engineering (AREA)
• Materials Engineering (AREA)
• Metallurgy (AREA)
• Organic Chemistry (AREA)
• Physics & Mathematics (AREA)
• Thermal Sciences (AREA)
• Crystallography & Structural Chemistry (AREA)
• Manufacturing & Machinery (AREA)
• Heat Treatment Of Steel (AREA)

Applications Claiming Priority (5)

Related Parent Applications (1)

Related Child Applications (1)

Publications (1)

Family

ID=42395758

Family Applications (2)

Family Applications After (1)

Country Status (7)

Cited By (22)

Families Citing this family (34)

Citations (1)

Family Cites Families (41)

• 2010
  • 2010-01-29 CN CN2013101775559A patent/CN103276291A/zh active Pending
  • 2010-01-29 EP EP10735967.1A patent/EP2392681B1/fr active Active
  • 2010-01-29 CA CA2809171A patent/CA2809171C/fr active Active
  • 2010-01-29 RU RU2011135941/02A patent/RU2478123C1/ru active
  • 2010-01-29 WO PCT/JP2010/051647 patent/WO2010087512A1/fr active Application Filing
  • 2010-01-29 US US13/146,751 patent/US20120018056A1/en not_active Abandoned
  • 2010-01-29 CN CN2010800063180A patent/CN102301015B/zh active Active
  • 2010-01-29 KR KR1020147005764A patent/KR20140041929A/ko not_active Application Discontinuation
  • 2010-01-29 KR KR1020117017827A patent/KR101686257B1/ko active IP Right Grant
  • 2010-01-29 CA CA2750291A patent/CA2750291C/fr active Active
  • 2010-01-29 KR KR1020167011804A patent/KR20160057492A/ko not_active Application Discontinuation
• 2016
  • 2016-12-12 US US15/375,410 patent/US9809869B2/en active Active

Patent Citations (1)

Non-Patent Citations (1)

Also Published As

Similar Documents

Legal Events