EP2380997A1 - Steel for weld construction having excellent high-temperature strength and low-temperature toughness and process for producing the steel - Google Patents

Steel for weld construction having excellent high-temperature strength and low-temperature toughness and process for producing the steel Download PDF

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EP2380997A1
EP2380997A1 EP09707108A EP09707108A EP2380997A1 EP 2380997 A1 EP2380997 A1 EP 2380997A1 EP 09707108 A EP09707108 A EP 09707108A EP 09707108 A EP09707108 A EP 09707108A EP 2380997 A1 EP2380997 A1 EP 2380997A1
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steel
less
temperature
strength
toughness
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French (fr)
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EP2380997B1 (en
EP2380997A4 (en
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Yoshiyuki Watanabe
Ryuji Uemori
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Nippon Steel Corp
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Nippon Steel Corp
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/04Ferrous alloys, e.g. steel alloys containing manganese
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0221Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the working steps
    • C21D8/0226Hot rolling
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D8/00Modifying the physical properties by deformation combined with, or followed by, heat treatment
    • C21D8/02Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
    • C21D8/0247Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
    • C21D8/0263Modifying 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
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/001Ferrous alloys, e.g. steel alloys containing N
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/004Very low carbon steels, i.e. having a carbon content of less than 0,01%
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/06Ferrous alloys, e.g. steel alloys containing aluminium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/22Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/24Ferrous alloys, e.g. steel alloys containing chromium with vanadium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/26Ferrous alloys, e.g. steel alloys containing chromium with niobium or tantalum
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/28Ferrous alloys, e.g. steel alloys containing chromium with titanium or zirconium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/38Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/42Ferrous alloys, e.g. steel alloys containing chromium with nickel with copper
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/44Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/46Ferrous alloys, e.g. steel alloys containing chromium with nickel with vanadium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/48Ferrous alloys, e.g. steel alloys containing chromium with nickel with niobium or tantalum
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/18Ferrous alloys, e.g. steel alloys containing chromium
    • C22C38/40Ferrous alloys, e.g. steel alloys containing chromium with nickel
    • C22C38/58Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/004Dispersions; Precipitations
    • CCHEMISTRY; METALLURGY
    • C21METALLURGY OF IRON
    • C21DMODIFYING 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
    • C21D2211/00Microstructure comprising significant phases
    • C21D2211/005Ferrite

Definitions

  • the present invention mainly targets fire-resistant steel for building structures aimed at maintaining the proof strength at the time of fires and other high temperature conditions, but is not limited to building applications and can also be applied to steel for welded structures for offshore structures, ships, bridges, various storage tanks, and a broad range of other applications.
  • the strength level of the steel plate mainly covered is a yield strength of 235 to 475 MPa and a tensile strength of 400 to 640 MPa, i.e., the classes generally called "40 kg” and "50 kg steels".
  • steel for general structures for which standards are set by the Japan Industrial Standard (JIS) etc. fall in strength starting from about 350°C, so the allowable temperature is about 350°C. That is, when using such a steel material for buildings, offices, homes, multistory parking structures, and other structures, to secure safety at the time of a fire, it is obligatory to apply a sufficient fire-resistant coating.
  • JIS Japan Industrial Standard
  • Japanese building laws stipulate that at the time of a fire, the temperature of steel materials not reach 350°C or more. This is because with such steel materials, at 350°C or so, the proof strength becomes about 2/3 that of ordinary temperature or falls below the required strength. For this reason, when utilizing a general steel material for a structure, it is necessary to apply a fire-resistant coating so that the temperature of the steel material does not reach 350°C.
  • fire-resistant steel enhanced in high temperature proof strength at high temperature tensile tests of 600°C etc. (below, when not particularly clearly indicated, a "high temperature” indicates 600°C and a “high temperature strength” indicates a high temperature proof strength) has been coming into use.
  • fire-resistant steel has Mo added to it for the purpose of maintaining the high temperature strength.
  • the market for Mo greatly fluctuates. While depending on the amount of addition as well, in many cases it results in a higher cost compared with the cost of fire-resistant coating. For this reason, development and commercialization of inexpensive fire-resistant steel to which Mo is not added have been awaited.
  • the present invention has as its object to obtain steel for welded structures excellent in high temperature strength without adding expensive Mo and also excellent in low temperature toughness - one of the basic performances of steel materials.
  • the present invention has as its object to obtain steel for welded structures excellent in high temperature strength without adding expensive Mo and also excellent in low temperature toughness - one of the basic performances of steel materials.
  • steel for welded structures having sufficient proof strength even at the time of a fire or other environment exposed to a high temperature can be supplied in large amounts inexpensively, so this can contribute to the improvement of safety of welded steel structures for a broad range of applications.
  • the point of the present invention is that to stably secure a high temperature strength at 600°C, instead of expensive Mo, a relatively small amount of C and co-addition of Cr and Nb are used for transformation strengthening and precipitation strengthening using Cr or Nb precipitates (carbonitrides).
  • the inventors discovered that by addition and inclusion of a suitable amount of Cr in an Mo-free composition, the hardenability of the steel is improved, the transformation temperature falls, and the hard structure including cementite becomes bainitic.
  • the present invention defines the amounts of not only Cr and Nb, but also individual elements such as C, Si, and Mn and the weld cracking parameter P CM and further limits the production conditions so as to not only achieve both excellent high temperature strength and low temperature toughness without using expensive Mo, but also secure various usage performances for steel for welded structures. Its gist is as follows:
  • C is limited to an extremely low level in high strength steel. This is closely related to the other elements and to the method of production. Even among the steel compositions, C has the greatest effect on the properties of a steel material. A lower limit of 0.003% is the smallest value for securing strength and preventing the weld and other heat affected zones from softening more than necessary.
  • the amount of C is too great, the hardenability rises more than necessary and the balance of strength and toughness of the steel material, the weldability, etc. are adversely affected. Further, as explained later, depending on the targeted plate thickness and strength, the accelerated cooling is stopped at a relatively low temperature in some cases. To suppress excessive hardening near the top and bottom surfaces of the steel material at that time or fluctuations in property in the plate thickness direction, the upper limit was made 0.05%.
  • the lower limit is preferably made 0.005%, more preferably 0.01%.
  • the upper limit is preferably made 0.04%, more preferably 0.03%.
  • Si is an element included in steel for deoxidation, but if overly added, the weldability and HAZ toughness deteriorate, so the upper limit was made 0.60%. Steel can be deoxidized by Ti and Al as well, so the content may be determined by the balance with these elements. However, from the viewpoint of the HAZ toughness, hardenability, etc., the lower the better. Zero addition is also possible. For this reason, the upper limit may be limited to 0.40%, 0.20%, or 0.10%. Note that when a steelmaking plant produces steel, even when using Ti and Al for deoxidation without the addition of Si, 0.01% or more of Si is generally included.
  • Mn is an element essential for securing room temperature strength and toughness.
  • the lower limit is 0.6%.
  • the content is 0.8% or more or 1.0% or more.
  • the upper limit was made 2.0%.
  • the content is made 1.8% or less, more preferably 1.6% or less or 1.4% or less.
  • S is preferably small in amount from the viewpoint of the low temperature toughness of the base material. If the content is large, the low temperature toughness of the base material and the weld zone is degraded, so the upper limit is made 0.010%. 0.008% or less, 0.006%, or 0.004% is more preferable. Of course, zero addition is also possible.
  • Cr is one of the most important elements in the present invention. To secure high temperature strength, together with Nb, addition of Cr is essential. This is because due to the effect of improvement of hardenability by Cr, the transformation temperature falls and the hard structure containing cementite becomes bainitic, so the room temperature and high temperature strengths are raised and further, because at the time of high temperature, precipitation strengthening by precipitates of Cr (carbonitrides) is utilized.
  • the content of Cr has to be a minimum of 0.20%. Preferably, it is 0.35% or more. 0.50% or more or 0.8% or 1.0% or more is more preferable. However, if the amount of addition is too great, deterioration of the toughness and weldability of the base material and weld zone is caused and economy is also lost, so the upper limit was made 1.5%. Preferably, it may be 1.3% or less.
  • Nb, along with Cr, is the most important element in the present invention.
  • Cr this is because precipitation strengthening by precipitates (carbonitrides) of Nb is utilized to secure high temperature strength.
  • the amount of addition is 0.010% or more. However, if the amount of addition is too great, this causes deterioration in the toughness of the weld zone, so the upper limit was made 0.05%. Preferably, the amount of addition is 0.045% or less, more preferably 0.030% or less. Note that addition of Nb also contributes to raising the non-recrystallization temperature of austenite and bringing out the effect of controlled rolling at the time of hot rolling to its maximum extent.
  • Mo is not intentionally added. Further, even when Mo is unintentionally mixed in as an impurity, it is restricted to 0.03% or less.
  • Al is an element generally included in steel for deoxidation. Deoxidation is also performed by Si and Ti, so the amount should be determined by the balance with these elements. However, if the amount of Al becomes large, not only will the cleanliness of the steel become poorer, but also the toughness of the weld metal will deteriorate, so the upper limit is made 0.060%. Preferably, it may be 0.040% or less. The smaller the amount the better. Zero addition is also possible. Note that when a steelmaking plant produces steel, even when not using Al for deoxidation, 0.001% or more of Al is generally included.
  • N is included in the steel as an unavoidable impurity, but bonds with Nb to form carbonitrides to increase the strength. Further, it forms TiN to enhance the properties of the steel as explained above. For this reason, as an amount of N, a minimum of 0.001% is required. Preferably, the amount may be 0.0015% or more. However, addition of an amount of N is harmful to the weld heat affected zone toughness and weldability. In the present invention steel, the upper limit is 0.006%. More preferably it may be 0.0045% or less.
  • V has substantially the same effects as Nb.
  • the role of V in the present invention is to complement the Nb.
  • V has a smaller effect than Nb and also has an effect on the hardenability, so upper and lower limits were set.
  • the lower limit was made 0.01% as the smallest amount at which the effect of addition of V can be reliably obtained.
  • the lower limit may be 0.025% or more.
  • the upper limit was made 0.10% considering also the effects on the later explained weld cracking parameter P CM .
  • the upper limit is 0.08% or less, more preferably 0.05% or less.
  • Ti is preferably added for improving the toughness of the base material and weld heat affected zone.
  • the reason why is that Ti, when the amount of Al is low (for example 0.003% or less), bonds with O to form precipitates mainly comprised of Ti 2 O 3 . These become nuclei for formation of intragranular ferrite and improve the toughness of the weld heat affected zone.
  • the fine TiN present in a steel material refines the weld heat affected zone structure and improves the toughness. To obtain these effects, Ti has to be a minimum of 0.005%. However, if too great, it forms TiC which degrades the low temperature toughness and weldability, so the upper limit was made 0.025%. Preferably, it is 0.020% or less.
  • the main purpose for further adding these elements to the basic compositions is to improve the strength, toughness, and other properties without detracting from the excellent characteristics of the invention steels. Therefore, the amounts of addition by nature should be self restricted.
  • Ni if not added in excess, improves the strength and toughness of the base material without having a detrimental effect on the weldability. To bring out these effects, addition of at least 0.05% is essential.
  • Cu exhibits substantially the same effects and phenomena as Ni.
  • the upper limit of 0.50% is set since in addition to deterioration of the weldability, excessive addition results in Cu cracks at the time of hot rolling and therefore difficult production.
  • the lower limit should be made the smallest amount by which the substantial effect can be obtained and therefore is 0.05%.
  • the upper limit may also be set to 0.30%.
  • the upper limit is made 0.003%. Preferably, it may be 0.002% or less.
  • SSCC sulfide stress corrosion cracking
  • HRC ⁇ 22 HV ⁇ 248
  • B which increases the hardenability, is not preferable.
  • B has the above effect of improving the strength, but there is the problem that addition of B causes deterioration of the heat affected zone toughness and other material quality, so to avoid these problems, it is more preferable to limit B to 0.0003% or less or not add it.
  • Mg has the action of controlling the growth of the austenite grains in the weld heat affected zone and refining so as to strengthen and toughen the weld zone. To obtain this effect, Mg has to be 0.0002% or more. On the other hand, if the amount of addition increases, the effect on the amount of addition becomes smaller, so this is not a wise course in terms of cost, so the upper limit was made 0.005%. Preferably, it may be 0.0035% or less.
  • the Ca and REM control the shape of the MnS and improve the low temperature toughness of the base material. In addition, they reduce the hydrogen induced cracking (HIC, SSC, and SOHIC) susceptibility under a wet hydrogen sulfide environment. To obtain these effects, a minimum of 0.0005% is necessary.
  • HIC hydrogen induced cracking
  • the value of the weld cracking parameter P CM is limited to 0.22% or less.
  • P CM C + Si / 30 + Mn / 20 + Cu / 20 + Ni / 60 + Cr / 20 + Mo / 15 + V / 10 + 5 ⁇ B
  • P CM is a parameter expressing the weldability. The lower, the better the weldability. In JIS G 3106 "Rolled Steels for Welded Structure", while differing depending on the strength level and the plate thickness, at the strictest, it is limited to 0.24% or less.
  • P CM is limited to 0.22% or less as a condition able to reliably prevent weld cold cracking even under harsher restraint conditions and environmental conditions.
  • the lower limit is not particularly set, but is restricted naturally from the ranges of limitation of the compositions.
  • the reason for limiting the heating temperature before the hot rolling to 1000 to 1300°C is to keep the austenite grains at the time of heating small and refine the rolled structure.
  • 1300°C is the upper limit temperature at which the austenite will not become extremely coarse at the time of heating. If the heating temperature exceeds this, the austenite grains become coarse mixed grains. The structure after transformation also becomes coarse, so the steel remarkably deteriorates in toughness.
  • the heating temperature is too low, depending on the plate thickness, not only does securing the later mentioned finish rolling temperature become difficult, but also the non-recrystallization temperature of the austenite is raised. From the viewpoint of the solubility of Nb for bringing out precipitation strengthening, the lower limit was made 1000°C. The most preferable heating temperature range is 1050 to 1250°C.
  • the steel material heated under the above-mentioned conditions is hot rolled at 800°C or more, then cooled.
  • the cooling means is not particularly an issue.
  • the material may also be allowed to stand in the atmosphere for cooling, but by accelerated cooling from a temperature of 750°C or more to a temperature of 550°C or less, it is possible to improve the characteristics of the steel material more.
  • the finish rolling temperature falls below 800°C, in the invention steels, where the amount of C is relatively small, the ferrite is liable to precipitate by transformation and ferrite is liable to be worked (rolled). This is not preferable from the viewpoint of securing the low temperature toughness.
  • the finish rolling temperature is limited to 800°C or more. Preferably, it may be 820°C or more.
  • the relatively low strength so-called "40 kg class steel” (for example, JIS standard SM400 and SN400 steel) after being hot rolled at 800°C or more can satisfy a predetermined strength even if allowed to stand in the atmosphere for cooling.
  • Accelerated cooling inherently increases the cooling rate in the transformation region and thereby refines the structure and simultaneously raises the strength and toughness. Therefore, unless started before the start of transformation or at least started before the end of transformation, it has substantially no meaning. For this reason, the accelerated cooling start temperature is limited to 750°C or more. This accelerated cooling has to be performed down to a temperature of 550°C or less in order to obtain this effect. With a temperature over 550°C, the transformation does not sufficiently proceed at the time of accelerated cooling and the refinement of the structure becomes insufficient.
  • the preferable start temperature of the accelerated cooling is 760°C or more.
  • the preferable range of stop temperature of the accelerated cooling is 520 to 300°C.
  • the cooling rate at the time of accelerated cooling depends on the steel compositions and the intended strength or low temperature toughness level, but the average cooling rate from the accelerated cooling start temperature to 550°C at a position of 1/4 the plate thickness from the surface in the direction of plate thickness is preferably made 3°C/sec or more.
  • Steel plates of various steel compositions were produced by a converter-continuous casting- plate rolling process and investigated for properties.
  • Table 1 shows the steel compositions of the comparative steels and the invention steels, while Table 2 shows the production conditions and properties of steel plates.
  • invention steels all have good properties. As opposed to this, it was learned that the steel plates not produced according to the present invention (comparative steels) were inferior in one or more of the propereties.
  • Comparative Steel 11 is high in the amount of C, so compared with the invention steels, both the base material and simulated HAZ are inferior in low temperature toughness.
  • Comparative Steel 12 does not have any Nb added. Further, Comparative Steel 13 is low in the amount of Cr. Both are therefore low in high temperature strength.
  • Comparative Steel 14 is low in the amount of C, so is low in high temperature strength.
  • Comparative Steel 15 is high in the amount of Cr, so both the base material and simulated HAZ are inferior in toughness.
  • Comparative Steel 16 is high in Nb and inferior in HAZ toughness.
  • Comparative Steels 17-1 to 3 are the same in compositions as the Invention Steel 5. However, Comparative Steel 17-1 is low in finish rolling temperature and as a result an accelerated cooling start temperature cannot be secured and ends up becoming low, so is low in both room temperature and high temperature strength. Comparative Steel 17-2 is low in accelerated cooling start temperature, so is low in both room temperature and high temperature strength. Comparative Steel 17-3 is high in accelerated cooling stop temperature, so is low in both room temperature and high temperature strength.
  • Comparative Steel 18 has individual elements and a method of production within the scope of the present invention and has an ordinary temperature and a high temperature strength or toughness etc. satisfying the characteristics required for the 490 MPa class, but has a high P CM , so cracks occurred in terms of the weldability ( y-groove weld cracking test).
  • steel for welded structures excellent in high temperature strength and low temperature toughness can be provided in large amounts inexpensively. As a result, it becomes possible to reduce or eliminate the fire-resistant coating for building structures. Further, in applications other than buildings as well, since the strength, toughness, and other basic performances are provided and further high temperature strength is also provided, it becomes possible obtain steel for welded structures able to be exposed to a high temperature and to enhance much more the safety of buildings.

Abstract

By heating a steel material comprising C: 0.003 to 0.05%, Si: 0.60% or less, Mn: 0.6 to 2.0%, P: 0.020% or less, S: 0.010% or less, Cr: 0.20 to 1.5%, Nb: 0.005 to 0.05%, Al: 0.060% or less, and N: 0.001 to 0.006%, further limiting, as an impurity, Mo to 0.03% or less, having a balance of iron and unavoidable impurities, and having a weld cracking parameter PCM value defined by PCM=C+Si/30+Mn/20+Cu/20+Ni/60+Cr/20+Mo/ 15+V/10+5B of 0.22% or less, to 1000 to 1300°C in temperature, finishing the hot rolling at 800°C or more in temperature, then cooling, steel for welded structures excellent in high temperature strength and low temperature toughness can be inexpensively provided.

Description

    TECHNICAL FIELD
  • The present invention mainly targets fire-resistant steel for building structures aimed at maintaining the proof strength at the time of fires and other high temperature conditions, but is not limited to building applications and can also be applied to steel for welded structures for offshore structures, ships, bridges, various storage tanks, and a broad range of other applications. Note that the strength level of the steel plate mainly covered is a yield strength of 235 to 475 MPa and a tensile strength of 400 to 640 MPa, i.e., the classes generally called "40 kg" and "50 kg steels".
  • PRIOR ART
  • So-called "fire-resistant steel" is disclosed in Japanese Patent Publication (A) No. 2-77523 and numerous other publications. However, almost all contain Mo. It is true that Mo is an element extremely effective in securing the high temperature proof strength of steel, but at the same time it is an expensive element.
  • In this regard, steel for general structures for which standards are set by the Japan Industrial Standard (JIS) etc. fall in strength starting from about 350°C, so the allowable temperature is about 350°C. That is, when using such a steel material for buildings, offices, homes, multistory parking structures, and other structures, to secure safety at the time of a fire, it is obligatory to apply a sufficient fire-resistant coating. Japanese building laws stipulate that at the time of a fire, the temperature of steel materials not reach 350°C or more. This is because with such steel materials, at 350°C or so, the proof strength becomes about 2/3 that of ordinary temperature or falls below the required strength. For this reason, when utilizing a general steel material for a structure, it is necessary to apply a fire-resistant coating so that the temperature of the steel material does not reach 350°C.
  • To eliminate or reduce this fire-resistant coating, fire-resistant steel enhanced in high temperature proof strength at high temperature tensile tests of 600°C etc. (below, when not particularly clearly indicated, a "high temperature" indicates 600°C and a "high temperature strength" indicates a high temperature proof strength) has been coming into use.
  • In general, fire-resistant steel has Mo added to it for the purpose of maintaining the high temperature strength. However, the market for Mo greatly fluctuates. While depending on the amount of addition as well, in many cases it results in a higher cost compared with the cost of fire-resistant coating. For this reason, development and commercialization of inexpensive fire-resistant steel to which Mo is not added have been awaited.
  • The present invention has as its object to obtain steel for welded structures excellent in high temperature strength without adding expensive Mo and also excellent in low temperature toughness - one of the basic performances of steel materials. For this purpose, by limiting the steel compositions to a specific range and further limiting the method of production, there is provided a method able to supply fire-resistant steel - excellent in high temperature strength, suppressed in weld cracking parameter, and securing low temperature toughness - industrially stably and further at a low cost.
  • According to the present invention, steel for welded structures having sufficient proof strength even at the time of a fire or other environment exposed to a high temperature can be supplied in large amounts inexpensively, so this can contribute to the improvement of safety of welded steel structures for a broad range of applications.
  • The point of the present invention is that to stably secure a high temperature strength at 600°C, instead of expensive Mo, a relatively small amount of C and co-addition of Cr and Nb are used for transformation strengthening and precipitation strengthening using Cr or Nb precipitates (carbonitrides).
  • That is, the inventors discovered that by addition and inclusion of a suitable amount of Cr in an Mo-free composition, the hardenability of the steel is improved, the transformation temperature falls, and the hard structure including cementite becomes bainitic.
  • Due to this, the ordinary temperature and high temperature strengths rise and the matrix is transformed at a relatively low temperature resulting in a fine bainitic structure. Because of this, the inventors discovered that at the time of a high temperature, carbonitrides of Cr and Nb alone or together resulting from the addition of Cr and Nb precipitate extremely finely in the matrix and a high temperature strength can be secured and maintained at a high level and thereby reached the present invention.
  • In the above way, fire-resistant steel not containing Mo is in itself extremely epochmaking. At the same time, since no Mo with its high hardenability is contained, this leads to improvement of the basic performance of steel for welded structures (strength and toughness) of course and also conversely the weldability and gas cutting performance.
  • The present invention defines the amounts of not only Cr and Nb, but also individual elements such as C, Si, and Mn and the weld cracking parameter PCM and further limits the production conditions so as to not only achieve both excellent high temperature strength and low temperature toughness without using expensive Mo, but also secure various usage performances for steel for welded structures. Its gist is as follows:
    1. (1) A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness characterized by comprising heating a steel material comprising, by mass%,
      C: 0.003 to 0.05%,
      Si: 0.60% or less,
      Mn: 0.6 to 2.0%,
      P: 0.020% or less,
      S: 0.010% or less,
      Cr: 0.20 to 1.5%,
      Nb: 0.005 to 0.05%,
      Al: 0.060% or less, and
      N: 0.001 to 0.006%,
      further limiting, as an impurity, Mo to 0.03% or less, having a balance of iron and unavoidable impurities, and having a weld cracking parameter PCM value defined by
      PCM=C+Si/30+Mn/20+Cu/20+Ni/60+Cr/20+Mo/15+V/10+5B of 0.22% or less, to 1000 to 1300°C in temperature, finish rolling temperature of 800°C or more, and then cooling.
    2. (2) A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness as set forth in claim 1, characterized by, after finishing said hot rolling, starting accelerated cooling from 750°C or more in temperature, and stopping the accelerated cooling at 550°C or less.
    3. (3) A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness as set forth in (1) or (2) characterized by further containing, by mass%, one or both of
      V: 0.01 to 0.10% and
      Ti: 0.005 to 0.025%.
    4. (4) A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness as set forth in any one of (1) to (3), characterized by further containing, by mass%, one or more of
      Ni: 0.05 to 0.50%,
      Cu: 0.05 to 0.50%,
      B: 0.0002 to 0.003%, and
      Mg: 0.0002 to 0.005%.
    5. (5) A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness as set forth in any one of (1) to (4), characterized by further containing, by mass%, one of
      Ca: 0.0005 to 0.004% and
      an REM: 0.0005 to 0.008%.
    6. (6) A steel for welded structures excellent in high temperature strength and low temperature toughness characterized by being obtained by heating a steel material comprising, by mass%,
      C: 0.003 to 0.05%,
      Si: 0.60% or less,
      Mn: 0.6 to 2.0%,
      P: 0.020% or less,
      S: 0.010% or less,
      Cr: 0.20 to 1.5%,
      Nb: 0.005 to 0.05%,
      Al: 0.060% or less, and
      N: 0.001 to 0.006%,
      further limiting, as an impurity, Mo to 0.03% or less, having a balance of iron and unavoidable impurities, and having a weld cracking parameter PCM value defined by
      PCM=C+Si/30+Mn/20+Cu/20+Ni/60+Cr/20+Mo/15+V/10+5B of 0.22% or less, to 1000 to 1300°C in temperature, finish rolling temperature of 800°C or more, and then cooling.
    BEST MODE FOR CARRYING OUT THE INVENTION
  • The ranges of addition of the different alloy elements defined in the present invention will be explained first.
  • C: 0.003 to 0.05%
  • C is limited to an extremely low level in high strength steel. This is closely related to the other elements and to the method of production. Even among the steel compositions, C has the greatest effect on the properties of a steel material. A lower limit of 0.003% is the smallest value for securing strength and preventing the weld and other heat affected zones from softening more than necessary.
  • If the amount of C is too great, the hardenability rises more than necessary and the balance of strength and toughness of the steel material, the weldability, etc. are adversely affected. Further, as explained later, depending on the targeted plate thickness and strength, the accelerated cooling is stopped at a relatively low temperature in some cases. To suppress excessive hardening near the top and bottom surfaces of the steel material at that time or fluctuations in property in the plate thickness direction, the upper limit was made 0.05%.
  • From the fluctuations in operation and balance with the other elements, to avoid a drop in strength, the lower limit is preferably made 0.005%, more preferably 0.01%. Further, to avoid excessive hardening by accelerated cooling and fluctuations in property, the upper limit is preferably made 0.04%, more preferably 0.03%.
  • Si: 0.60% or less
  • Si is an element included in steel for deoxidation, but if overly added, the weldability and HAZ toughness deteriorate, so the upper limit was made 0.60%. Steel can be deoxidized by Ti and Al as well, so the content may be determined by the balance with these elements. However, from the viewpoint of the HAZ toughness, hardenability, etc., the lower the better. Zero addition is also possible. For this reason, the upper limit may be limited to 0.40%, 0.20%, or 0.10%. Note that when a steelmaking plant produces steel, even when using Ti and Al for deoxidation without the addition of Si, 0.01% or more of Si is generally included.
  • Mn: 0.6 to 2.0%
  • Mn is an element essential for securing room temperature strength and toughness. The lower limit is 0.6%. Preferably, the content is 0.8% or more or 1.0% or more. However, if the amount of Mn is too large, the hardenability rises and the weldability and HAZ toughness are degraded. Not only that, but also center segregation at the continuously cast slab is enhanced, so the upper limit was made 2.0%. Preferably, the content is made 1.8% or less, more preferably 1.6% or less or 1.4% or less.
  • P: 0.020% or less
  • P, if small in amount, tends to reduce the intergranular fractures at the HAZ, so the smaller, the better. If the content is large, it degrades the low temperature toughness of the base material and the weld zone, so the upper limit is made 0.020%. 0.015% or less, 0.010% or less, or 0.008% or less is more preferable. Of course, zero addition is also possible.
  • S: 0.010% or less
  • S is preferably small in amount from the viewpoint of the low temperature toughness of the base material. If the content is large, the low temperature toughness of the base material and the weld zone is degraded, so the upper limit is made 0.010%. 0.008% or less, 0.006%, or 0.004% is more preferable. Of course, zero addition is also possible.
  • Cr: 0.20 to 1.5%
  • Cr is one of the most important elements in the present invention. To secure high temperature strength, together with Nb, addition of Cr is essential. This is because due to the effect of improvement of hardenability by Cr, the transformation temperature falls and the hard structure containing cementite becomes bainitic, so the room temperature and high temperature strengths are raised and further, because at the time of high temperature, precipitation strengthening by precipitates of Cr (carbonitrides) is utilized.
  • To obtain these effects, the content of Cr has to be a minimum of 0.20%. Preferably, it is 0.35% or more. 0.50% or more or 0.8% or 1.0% or more is more preferable. However, if the amount of addition is too great, deterioration of the toughness and weldability of the base material and weld zone is caused and economy is also lost, so the upper limit was made 1.5%. Preferably, it may be 1.3% or less.
  • Nb: 0.005 to 0.05%
  • Nb, along with Cr, is the most important element in the present invention. In the same way as Cr, this is because precipitation strengthening by precipitates (carbonitrides) of Nb is utilized to secure high temperature strength.
  • For this reason, at least 0.005% is necessary. Preferably, the amount of addition is 0.010% or more. However, if the amount of addition is too great, this causes deterioration in the toughness of the weld zone, so the upper limit was made 0.05%. Preferably, the amount of addition is 0.045% or less, more preferably 0.030% or less. Note that addition of Nb also contributes to raising the non-recrystallization temperature of austenite and bringing out the effect of controlled rolling at the time of hot rolling to its maximum extent.
  • Due to the above addition of Cr and Nb, it is possible to secure high temperature strength even under Mo-free conditions. Therefore, in the present invention, Mo is not intentionally added. Further, even when Mo is unintentionally mixed in as an impurity, it is restricted to 0.03% or less.
  • Al: 0.060% or less
  • Al is an element generally included in steel for deoxidation. Deoxidation is also performed by Si and Ti, so the amount should be determined by the balance with these elements. However, if the amount of Al becomes large, not only will the cleanliness of the steel become poorer, but also the toughness of the weld metal will deteriorate, so the upper limit is made 0.060%. Preferably, it may be 0.040% or less. The smaller the amount the better. Zero addition is also possible. Note that when a steelmaking plant produces steel, even when not using Al for deoxidation, 0.001% or more of Al is generally included.
  • N: 0.001 to 0.006%
  • N is included in the steel as an unavoidable impurity, but bonds with Nb to form carbonitrides to increase the strength. Further, it forms TiN to enhance the properties of the steel as explained above. For this reason, as an amount of N, a minimum of 0.001% is required. Preferably, the amount may be 0.0015% or more. However, addition of an amount of N is harmful to the weld heat affected zone toughness and weldability. In the present invention steel, the upper limit is 0.006%. More preferably it may be 0.0045% or less.
  • Next, the reasons for addition of V and Ti which may be included in accordance with need will be explained.
  • V: 0.01 to 0.10%
  • V has substantially the same effects as Nb. The role of V in the present invention is to complement the Nb. However, V has a smaller effect than Nb and also has an effect on the hardenability, so upper and lower limits were set. The lower limit was made 0.01% as the smallest amount at which the effect of addition of V can be reliably obtained. Preferably, the lower limit may be 0.025% or more. The upper limit was made 0.10% considering also the effects on the later explained weld cracking parameter PCM. Preferably, the upper limit is 0.08% or less, more preferably 0.05% or less.
  • Ti: 0.005 to 0.025%
  • Ti is preferably added for improving the toughness of the base material and weld heat affected zone. The reason why is that Ti, when the amount of Al is low (for example 0.003% or less), bonds with O to form precipitates mainly comprised of Ti2O3. These become nuclei for formation of intragranular ferrite and improve the toughness of the weld heat affected zone.
  • Further, Ti bonds with N to form TiN which finely precipitates in the steel material and is effective for suppressing coarsening of the γ grains at the time of heating and refining the rolled structure. Further, the fine TiN present in a steel material refines the weld heat affected zone structure and improves the toughness. To obtain these effects, Ti has to be a minimum of 0.005%. However, if too great, it forms TiC which degrades the low temperature toughness and weldability, so the upper limit was made 0.025%. Preferably, it is 0.020% or less.
  • Next, the reasons for addition of Ni, Cu, B, and Mg will be explained.
  • The main purpose for further adding these elements to the basic compositions is to improve the strength, toughness, and other properties without detracting from the excellent characteristics of the invention steels. Therefore, the amounts of addition by nature should be self restricted.
  • Ni: 0.05 to 0.50%
  • Ni, if not added in excess, improves the strength and toughness of the base material without having a detrimental effect on the weldability. To bring out these effects, addition of at least 0.05% is essential.
  • On the other hand, excessive addition is not only expensive, but also is not preferable for the weldability. Further, if adding a large amount of Ni, the possibility of inducing stress corrosion cracking (SCC) in liquid ammonia has been pointed out. According to experiments of the inventors, addition of up to 1.0% does not greatly degrade the weldability or SCC in liquid ammonia and rather has a greater effect in improving the strength and toughness, but giving priority to economy, the upper limit was made 0.50%. Further, when giving priority to economy, the upper limit may also be set to 0.35%.
  • Cu: 0.05 to 0.50%
  • Cu exhibits substantially the same effects and phenomena as Ni. The upper limit of 0.50% is set since in addition to deterioration of the weldability, excessive addition results in Cu cracks at the time of hot rolling and therefore difficult production. The lower limit should be made the smallest amount by which the substantial effect can be obtained and therefore is 0.05%. When giving priority to economy, the upper limit may also be set to 0.30%.
  • B: 0.0002 to 0.003%
  • B segregates at the austenite grain boundaries and suppresses formation of ferrite to thereby improve the hardenability and contribute to improvement of the strength. To obtain this effect, a minimum of 0.0002% or more is required.
  • However, with addition of too much, not only would the effect of improvement of the hardenability become saturated, but also B precipitates harmful to the toughness might be formed, so the upper limit is made 0.003%. Preferably, it may be 0.002% or less. Note that in cases such as steel for storage tanks etc. where stress corrosion cracking is a concern, reduction of the hardness of the base material and weld heat affected zone often becomes the point (for example, to prevent sulfide stress corrosion cracking (SSCC), in terms of Rockwell hardness, HRC≤22 (HV≤248) is considered essential). In such a case, addition of B, which increases the hardenability, is not preferable. Note that B has the above effect of improving the strength, but there is the problem that addition of B causes deterioration of the heat affected zone toughness and other material quality, so to avoid these problems, it is more preferable to limit B to 0.0003% or less or not add it.
  • Mg: 0.0002 to 0.005%
  • Mg has the action of controlling the growth of the austenite grains in the weld heat affected zone and refining so as to strengthen and toughen the weld zone. To obtain this effect, Mg has to be 0.0002% or more. On the other hand, if the amount of addition increases, the effect on the amount of addition becomes smaller, so this is not a wise course in terms of cost, so the upper limit was made 0.005%. Preferably, it may be 0.0035% or less.
  • Next, the reasons for addition of Ca or REM will be explained.
  • Ca: 0.0005 to 0.004% REM: 0.0005 to 0.008%
  • The Ca and REM control the shape of the MnS and improve the low temperature toughness of the base material. In addition, they reduce the hydrogen induced cracking (HIC, SSC, and SOHIC) susceptibility under a wet hydrogen sulfide environment. To obtain these effects, a minimum of 0.0005% is necessary.
  • However, addition of too much conversely causes the cleanliness of the steel to deteriorate and raises the base material toughness and hydrogen induced cracking (HIC, SSC, and SOHIC) susceptibility under a wet hydrogen sulfide environment, so the upper limits of the amounts of addition were respectively made, for Ca and REM, 0.004% and 0.008%. Preferably, the limits may be made 0.003% and 0.006% or less. Note that Ca and REM have substantially equivalent effects, so it is sufficient to add either of these in the above range. Addition of both is also possible.
  • Even if limiting the individual elements of the steel, unless the system of compositions as a whole is suitable, excellent characteristics cannot be obtained. In the present invention, from the contents of the different elements (mass%), the value of the weld cracking parameter PCM, defined by the following formula, is limited to 0.22% or less. P CM = C + Si / 30 + Mn / 20 + Cu / 20 + Ni / 60 + Cr / 20 + Mo / 15 + V / 10 + 5 B
    Figure imgb0001
  • PCM is a parameter expressing the weldability. The lower, the better the weldability. In JIS G 3106 "Rolled Steels for Welded Structure", while differing depending on the strength level and the plate thickness, at the strictest, it is limited to 0.24% or less.
  • According to the broad range of various weld crack tests of the inventors, PCM is limited to 0.22% or less as a condition able to reliably prevent weld cold cracking even under harsher restraint conditions and environmental conditions. Note that the lower limit is not particularly set, but is restricted naturally from the ranges of limitation of the compositions.
  • Next, the production conditions will be explained.
  • The reason for limiting the heating temperature before the hot rolling to 1000 to 1300°C is to keep the austenite grains at the time of heating small and refine the rolled structure. 1300°C is the upper limit temperature at which the austenite will not become extremely coarse at the time of heating. If the heating temperature exceeds this, the austenite grains become coarse mixed grains. The structure after transformation also becomes coarse, so the steel remarkably deteriorates in toughness.
  • On the other hand, if the heating temperature is too low, depending on the plate thickness, not only does securing the later mentioned finish rolling temperature become difficult, but also the non-recrystallization temperature of the austenite is raised. From the viewpoint of the solubility of Nb for bringing out precipitation strengthening, the lower limit was made 1000°C. The most preferable heating temperature range is 1050 to 1250°C.
  • The steel material heated under the above-mentioned conditions is hot rolled at 800°C or more, then cooled. The cooling means is not particularly an issue. The material may also be allowed to stand in the atmosphere for cooling, but by accelerated cooling from a temperature of 750°C or more to a temperature of 550°C or less, it is possible to improve the characteristics of the steel material more.
  • If the finish rolling temperature falls below 800°C, in the invention steels, where the amount of C is relatively small, the ferrite is liable to precipitate by transformation and ferrite is liable to be worked (rolled). This is not preferable from the viewpoint of securing the low temperature toughness. For this reason, the finish rolling temperature is limited to 800°C or more. Preferably, it may be 820°C or more.
  • The relatively low strength so-called "40 kg class steel" (for example, JIS standard SM400 and SN400 steel) after being hot rolled at 800°C or more can satisfy a predetermined strength even if allowed to stand in the atmosphere for cooling.
  • However, even with 50 kg class steel (for example, JIS standard SM490 and SN490 steel) or 40 kg class steel, if the plate thickness becomes greater, it becomes difficult to secure stability of the strength as cooled by standing in the atmosphere, so accelerated cooling from a temperature of 750°C or more after hot rolling at 800°C or more is preferable. Accelerated cooling after rolling improves the characteristics of the steel material and does not harm the excellent features of the present invention.
  • Accelerated cooling inherently increases the cooling rate in the transformation region and thereby refines the structure and simultaneously raises the strength and toughness. Therefore, unless started before the start of transformation or at least started before the end of transformation, it has substantially no meaning. For this reason, the accelerated cooling start temperature is limited to 750°C or more. This accelerated cooling has to be performed down to a temperature of 550°C or less in order to obtain this effect. With a temperature over 550°C, the transformation does not sufficiently proceed at the time of accelerated cooling and the refinement of the structure becomes insufficient. The preferable start temperature of the accelerated cooling is 760°C or more. The preferable range of stop temperature of the accelerated cooling is 520 to 300°C.
  • Note that the cooling rate at the time of accelerated cooling depends on the steel compositions and the intended strength or low temperature toughness level, but the average cooling rate from the accelerated cooling start temperature to 550°C at a position of 1/4 the plate thickness from the surface in the direction of plate thickness is preferably made 3°C/sec or more.
  • Further, even if tempering after rolling at the Ac1 temperature or less, the excellent features of the present invention are not impaired. This cancels out the unevenness of cooling and improves the uniformity of quality in the plate, so is rather preferable.
  • EXAMPLES
  • Steel plates of various steel compositions (thickness 19 to 100 mm) were produced by a converter-continuous casting- plate rolling process and investigated for properties.
  • Table 1 shows the steel compositions of the comparative steels and the invention steels, while Table 2 shows the production conditions and properties of steel plates.
  • The steel plates produced in accordance with the present invention (invention steels) all have good properties. As opposed to this, it was learned that the steel plates not produced according to the present invention (comparative steels) were inferior in one or more of the propereties.
  • Comparative Steel 11 is high in the amount of C, so compared with the invention steels, both the base material and simulated HAZ are inferior in low temperature toughness.
  • Comparative Steel 12 does not have any Nb added. Further, Comparative Steel 13 is low in the amount of Cr. Both are therefore low in high temperature strength.
  • Comparative Steel 14 is low in the amount of C, so is low in high temperature strength.
  • Comparative Steel 15 is high in the amount of Cr, so both the base material and simulated HAZ are inferior in toughness.
  • Comparative Steel 16 is high in Nb and inferior in HAZ toughness.
  • Comparative Steels 17-1 to 3 are the same in compositions as the Invention Steel 5. However, Comparative Steel 17-1 is low in finish rolling temperature and as a result an accelerated cooling start temperature cannot be secured and ends up becoming low, so is low in both room temperature and high temperature strength. Comparative Steel 17-2 is low in accelerated cooling start temperature, so is low in both room temperature and high temperature strength. Comparative Steel 17-3 is high in accelerated cooling stop temperature, so is low in both room temperature and high temperature strength.
  • Comparative Steel 18 has individual elements and a method of production within the scope of the present invention and has an ordinary temperature and a high temperature strength or toughness etc. satisfying the characteristics required for the 490 MPa class, but has a high PCM, so cracks occurred in terms of the weldability ( y-groove weld cracking test). Table 1
    Class Steel Chemical compositions (mass%)
    C Si Mn P S Cr Nb Al N Mo Others PCM 1)
    I 1 0.003 0.31 0.95 0.006 0.003 0.81 0.018 0.028 0.030 0.01 0.011Ti, 0.0010B 0.107
    n 2 0.01 0.16 1.31 0.004 0.002 0.65 0.020 0.033 0.024 0.01 0.18Cu, 0.18Ni 0.126
    v 3 0.02 0.57 1.87 0.005 0.002 1.45 0.007 0.021 0.029 0.02 0.20Ni, 0.052V, 0.009Ti 0.215
    . 4 0.02 0.22 1.45 0.007 0.002 0.41 0.012 0.023 0.051 0 0.062V 0.127
    s 5 0.03 0.38 1.48 0.007 0.004 0.68 0.033 0.006 0.028 0.01 0.21Cu, 0.22Ni, 0.010Ti, 0.0012Mg 0.166
    t 6 0.03 0.19 1.66 0.006 0.006 1.01 0.028 0.005 0.022 0.03 0.0009B, 0.0014Ca 0.176
    e 7 0.03 0.44 0.62 0.007 0.003 0.22 0.047 0.045 0.043 0.01 0.32Cu, 0.32Ni, 0.062V, 0.0018REM 0.115
    e 8 0.04 0.27 1.31 0.005 0.002 0.50 0.024 0.003 0.036 0 0.140
    l 9 0.04 0.08 1.81 0.005 0.004 1.20 0.019 0.032 0.027 0 0.25Cu, 0.25Ni 0.210
    10 0.05 0.24 1.89 0.006 0.005 0.56 0.021 0.016 0.032 0.02 0.014Ti, 0.0013B, 0.0012Ca 0.188
    19 0.02 0.20 1.57 0.005 0.004 0.61 0.026 0.022 0.028 0.01 0.009Ti 0.136
    C 11 0.06 0.23 28 0.006 0.004 0.41 0.034 0.020 0.030 0.02 0.012Ti 0.153
    o 12 0.02 28 56 0.007 0.002 0.80 0 0.027 0.035 0.01 0.25Ni 0.153
    m 13 0.03 29 27 0.008 0.008 0.14 0.020 0.028 0.026 0.01 0.0015Ca 0.111
    p 14 0.001 33 57 0.006 0.004 0.69 0.018 0.031 0.032 0 0.125
    . 15 0.04 25 31 0.008 0.005 1.72 0.025 0.024 0.027 0 0.200
    s 16 0.04 31 25 0.006 0.004 0.51 0.065 0.033 0.025 0.02 0.139
    t 17 0.03 03 48 0.007 0.004 0.68 0.028 0.006 0.028 0.01 0.21Cu, 0.22Ni, 0.010Ti, 0.0012Mg 0.166
    e 18 0.04 39 83 0.007 0.005 1.38 0.030 0.031 0.033 0.02 0.25Cu, 0.25Ni, 0.070V, 0.011Ti 0.237
    e
    l
    1) PCM=C+Si/30+Mn/20+Cu/20+Ni/60+Cr/20+Mo/15+V/10+5B
    Table 2
    Class Steel Targeted strength grade Heating temp. (°C) Finish rolling temp. (°C) Acc. cooling start temp. (°C) Acc. cooling stop temp. (°C) Plate thick. (mm) Yield strength (MPa) Tensile strength (MPa) vTrs (°C) Proof strength at 600°C (MPa)1) Simulated HAZ toughness2), vE0 (J) Root cracking at y-crack test without preheating (room temp.)3)
    I 1 400MPa 1250 920 980 340 50 332 477 -98 182 163 None
    n 2 490MPa 1200 820 780 460 25 386 551 -84 250 124 None
    v 3 400MPa 1200 850 - - 40 395 548 -81 246 109 None
    . 4 490MPa 1280 860 820 480 50 431 545 -75 242 112 None
    s 5 490MPa 1200 900 860 430 32 433 563 -78 256 98 None
    t 6 490MPa 1100 950 930 450 100 338 518 -71 237 106 None
    e 7 490MPa 1100 930 900 300 80 376 522 -65 234 121 None
    e 8 490MPa 1050 870 840 410 60 386 536 -68 245 101 None
    1 9 490MPa 1150 810 - - 19 454 582 -75 261 126 None
    10 490MPa 1150 850 800 290 50 414 547 -67 243 95 None
    19 490MPa 1150 840 - - 28 298 452 -80 164 156 None
    C 11 490MPa 1150 860 820 230 50 408 553 -12 248 18 None
    o 12 400MPa 1150 850 800 250 40 283 479 -78 142 141 None
    m 13 490MPa 1150 850 - - 40 376 529 -67 197 130 None
    p 14 400MPa 1200 850 - - 40 319 487 -86 151 139 None
    . 15 490MPa 1200 850 - - 40 362 541 -10 236 23 None
    s 16 490MPa 1200 900 - - 40 348 561 -55 251 14 None
    t 17-1 490MPa 1100 750 720 280 32 431 488 -82 198 111 None
    e 17-2 490MPa 1100 800 730 300 32 322 484 -79 195 106 None
    e 17-3 490MPa 1100 830 770 600 32 317 496 -80 197 99 None
    1 18 490MPa 1100 810 - - 40 363 527 -21 220 73 Yes
    1) Judgment criteria for passage: 400 MPa class steel: 157 MPa or more (235x(2/3)), 490 MPa steel, 217 MPa or more (325x(2/3))
    2) Charpy impact absorption energy of simulated heat cycle (conditions: after holding at 1400°Cx10 sec, then cooling from 800 to 500°C by 100 sec) (average value of three samples)
    3) y-groove weld cracking test (JIS Z 3158)
  • INDUSTRIAL APPLICABILITY
  • According to the present invention, steel for welded structures excellent in high temperature strength and low temperature toughness can be provided in large amounts inexpensively. As a result, it becomes possible to reduce or eliminate the fire-resistant coating for building structures. Further, in applications other than buildings as well, since the strength, toughness, and other basic performances are provided and further high temperature strength is also provided, it becomes possible obtain steel for welded structures able to be exposed to a high temperature and to enhance much more the safety of buildings.

Claims (6)

  1. A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness characterized by comprising heating a steel material comprising, by mass%,
    C: 0.003 to 0.05%,
    Si: 0.60% or less,
    Mn: 0.6 to 2.0%,
    P: 0.020% or less,
    S: 0.010% or less,
    Cr: 0.20 to 1.5%,
    Nb: 0.005 to 0.05%,
    Al: 0.060% or less, and
    N: 0.001 to 0.006%,
    further limiting, as an impurity, Mo to 0.03% or less, having a balance of iron and unavoidable impurities, and having a weld cracking parameter PCM value defined by
    PCM=C+Si/30+Mn/20+Cu/20+Ni/60+Cr/20+Mo/15+V/10+5B of 0.22% or less, to 1000 to 1300°C in temperature, finishing the hot rolling at a temperature of 800°C or more, and then cooling.
  2. A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness as set forth in claim 1, characterized by, after finishing said hot rolling, starting accelerated cooling from 750°C or more in temperature, and stopping the accelerated cooling at 550°C or less.
  3. A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness as set forth in claim 1 or 2 characterized by further containing, by mass%, one or both of
    V: 0.01 to 0.10% and
    Ti: 0.005 to 0.025%.
  4. A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness as set forth in any one of claims 1 to 3, characterized by further containing, by mass%, one or more of
    Ni: 0.05 to 0.50%,
    Cu: 0.05 to 0.50%,
    B: 0.0002 to 0.003%, and
    Mg: 0.0002 to 0.005%.
  5. A method of production of steel for welded structures excellent in high temperature strength and low temperature toughness as set forth in any one of claims 1 to 4, characterized by further containing, by mass%, one of
    Ca: 0.0005 to 0.004% and
    an REM: 0.0005 to 0.008%.
  6. A steel for welded structures excellent in high temperature strength and low temperature toughness characterized by being obtained by heating a steel material comprising, by mass%,
    C: 0.003 to 0.05%,
    Si: 0.60% or less,
    Mn: 0.6 to 2.0%,
    P: 0.020% or less,
    S: 0.010% or less,
    Cr: 0.20 to 1.5%,
    Nb: 0.005 to 0.05%,
    Al: 0.060% or less, and
    N: 0.001 to 0.006%,
    further limiting, as an impurity, Mo to 0.03% or less, having a balance of iron and unavoidable impurities, and having a weld cracking parameter PCM value defined by
    PCM=C+Si/30+Mn/20+Cu/20+Ni/60+Cr/20+Mo/15+V/10+5B of 0.22% or less, to 1000 to 1300°C in temperature, finishing the hot rolling at a temperature of 800°C or more, and then cooling.
EP09707108.8A 2009-01-15 2009-01-15 Steel for welded structures excellent in high temperature strength and low temperature toughness and method of production of same Active EP2380997B1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/JP2009/050906 WO2010082361A1 (en) 2009-01-15 2009-01-15 Steel for weld construction having excellent high-temperature strength and low-temperature toughness and process for producing the steel

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EP2380997A1 true EP2380997A1 (en) 2011-10-26
EP2380997A4 EP2380997A4 (en) 2016-12-28
EP2380997B1 EP2380997B1 (en) 2020-01-08

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US (1) US20110262298A1 (en)
EP (1) EP2380997B1 (en)
JP (1) JP4834149B2 (en)
KR (1) KR101189263B1 (en)
CN (1) CN101849026B (en)
BR (1) BRPI0901011B1 (en)
WO (1) WO2010082361A1 (en)

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KR20100105821A (en) 2010-09-30
BRPI0901011B1 (en) 2019-09-10
CN101849026A (en) 2010-09-29
WO2010082361A1 (en) 2010-07-22
JP4834149B2 (en) 2011-12-14
EP2380997B1 (en) 2020-01-08
KR101189263B1 (en) 2012-10-09
CN101849026B (en) 2012-07-04
JPWO2010082361A1 (en) 2012-06-28
BRPI0901011A2 (en) 2015-11-24
EP2380997A4 (en) 2016-12-28
US20110262298A1 (en) 2011-10-27

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