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 of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment
  • C21D8/02—Modifying the physical properties of ferrous metals or ferrous alloys by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
  • C21D8/0247—Modifying the physical properties of ferrous metals or ferrous alloys 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 of ferrous metals or ferrous alloys 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
  • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
  • C22C—ALLOYS
  • C22C38/00—Ferrous alloys, e.g. steel alloys
  • C22C38/004—Very low carbon steels, i.e. having a carbon content of less than 0,01%
• • 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
  • C22C38/12—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
  • 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
• • C—CHEMISTRY; METALLURGY
  • C21—METALLURGY OF IRON
  • C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
  • C21D2211/00—Microstructure comprising significant phases
  • C21D2211/005—Ferrite

Definitions

• the present invention relates to a method for producing a high-tensile-strength low alloy carbon steel (in the form of a steel sheet, a steel pipe, a section steel or a wire rod), for a building structure, the high-tensile-strength steel showing an excellent high temperature strength during a relatively short span of about one hour in the temperature range from 600°C to 800°C and being used for a general structure in the field of building construction, civil engineering, an offshore structure, shipbuilding, a reservoir tank or the like.
• the reason for the above regulation is that the proof stress of the above-mentioned steel at about 350°C becomes about two-thirds of that at room temperature and thus it falls short of the required strength.
• a fire-resistant coating is applied thereto so that the temperature of the steel may not reach 350°C during a fire. Therefore, the cost for the fire-resistant coating goes up in comparison with the cost of the steel and a large increase in the construction cost is inevitable.
• Japanese Unexamined Patent Publication Nos. H2-77523 and H10-68044 disclose that a steels usable at a temperature of not lower than 600°C is generally called "a fire-resistant steel.”
• a fire-resistant steel As an example of the relevant invention, Japanese Unexamined Patent Publication No. H2-77523 proposes a fire-resistant steel having such a high temperature strength that the yield strength thereof at 600°C is not less than two-thirds (about 70%) of that at room temperature.
• the generally adopted criterion is that a yield strength at 600°C is not less than two-thirds of that at room temperature.
• Japanese Unexamined Patent Publication No. H2-77523 discloses a steel, to which considerable amounts of Mo and Nb are added, that can secure a proof stress at 600°C of not less than 70% of the proof stress at room temperature, but it does not describe a proof stress at 700°C or 800°C.
• a building structure to which a steel not coated with fire-resistant coating is applicable is limited to an architecture having an open space such as a multi-level car parking tower or an atrium and therefore the application of the steel not coated with a fire-resistant coating is substantially limited.
• Japanese Unexamined patent Publication No. H10-68044 discloses a technology that secures a proof stress at 700°C being not less than 56% of the proof stress at room temperature by making the microstructure of a steel, to which considerable amounts of Mo and Nb are added, composed of a bainite structure, but it does not describe a proof stress at 800°C.
• the present inventors have recently disclosed a fire-resistant steel withstanding 850°C in Japanese Unexamined Patent Publication No. 2002-105585.
• the invented steel secures effective precipitates even at a high temperature and obtains fire resistance at 850°C by adding comparatively large amounts of alloying elements such as Al, Ti, etc.
• alloying elements such as Al, Ti, etc.
• it is not suitable for the steel to be applied to a welded structure.
• the guaranteed fire-resistant temperature has been 600°C to 700°C at the highest and therefore the development of a steel that can be used at a temperature of 700°C or 800°C without the application of fire-resistant coating and thus allows a fire-resistant coating process to be eliminated, has long been sought for.
• the object of the present invention is to provide: a high-tensile-strength steel that is excellent in high temperature strength in the temperature range from 600°C to 800°C and in weldability and is used in the field of building construction, civil engineering or the like; and a production method that makes it possible to stably supply the steel in an industrial scale.
• the gist of the present invention is as follows:
• the present inventors have proposed steels excellent in high temperature strength at 600°C and 700°C and the steels excellent in high temperature strength at 600°C have already been used in various fields including building construction.
• a steel In a fire resistance design, a steel is well accepted as long as the steel maintains high strength for the duration of a fire. That is, it is not necessary to consider such long lasting strength as required of a conventional heat-resistant steel and a steel is well accepted as long as the yield strength of the steel is maintained for a relatively short time at a high temperature.
• a steel can be sufficiently used as a fire-resistant steel withstanding 800°C as long as the yield strength of the steel is secured for a short retention time of about 30 minutes at a high temperature of 800°C.
• the performance of a conventional fire-resistant steel has been regulated so that a yield strength at a high temperature is not less than two-thirds of that at room temperature.
• the range of the strength of a steel in the actual design of a steel construction is about 0.2 to 0.4 time the lower limit of the yield strength at room temperature, it is necessary for the steel to satisfy the expression p ⁇ - 0.0029 x T + 2.48 when the steel temperature T (°C) is within the range from 600°C to 800°C, wherein p is a stress drop ratio (a yield stress at a high temperature/a yield stress at room temperature) that is obtained by converting a yield stress normalized by using a yield stress at room temperature.
• a microstructure may be made composed of a single structure of bainite.
• a low C content has the effects of enhancing the thermodynamic stability of bainite or a composite structure composed of ferrite and bainite at a high temperature and also raising the temperature (Ac 1 ) at which a structure reversely transforms into austenite.
• Ac 1 the temperature at which a structure reversely transforms into austenite.
• the present inventors investigated the control of a microstructure and the enhancement of high temperature strength, as a result, found that an appropriate the amount B addition was effective for the stabilization of production, and established the present invention.
• a steel in this category is generally required to have such weldability as required of a conventional steel for a welded structure since the steel may be used for a welded structure, and therefore it has been a very difficult challenge to achieve such a steel excellent in strength at a high temperature of 700°C to 800°C.
• the present inventors carried out intensive studies to solve the problem, and found that, in order to obtain a high temperature strength in the temperature range from 700°C to 800°C, it was effective to enhance precipitation hardening of a steel by the combined addition of alloying elements such as Mo, Nb, v, Ti, etc., in order to increase dislocation density by making a microstructure composed of bainite, and further to delay the recovery of the dislocation by dissolved Mo, Nb and V and somewhat by dissolved Ti.
• alloying elements such as Mo, Nb, v, Ti, etc.
• the present inventors further found that, in order to simultaneously secure all of a strength at 700°C to 800°C, a strength at room temperature, and a desired a stress drop ratio p from room temperature to a high temperature, it was important to make a microstructure comprising a composite structure composed of ferrite and bainite or a single structure composed of bainite and, at the same time, to obtain the thermal stability of the matrix structure at a high temperature and the adequate effects of conformable precipitation hardening and dislocation recovery delay by controlling the amounts of alloying elements addition in appropriate amounts. Furthermore, in order to secure a low yield ratio, it is necessary to make a microstructure comprising an adequate composite structure composed of ferrite and bainite.
• the yield strength of a steel begins to drop sharply from a temperature close to 450°C. This is because, as a temperature rises, thermal activation energy drops and resistance to dislocation slip movement, which has been effective at a low temperature, becomes ineffective.
• Cr carbide, Mo carbide and the like which are utilized for strengthening a steel in a temperature of around lower than 700°C, function as effective resistance to dislocation slip movement up to a high temperature of about 600°C, but they dissolve again at a high temperature of 800°C or so and therefore can scarcely maintain the strengthening effect.
• the present inventors investigated single or composite structures of various precipitates having higher stability at a high temperature. As a result, it was found that precipitates formed by combining Mo with Nb, Ti and V had high stability at a high temperature and also a high strengthening effect at 700°C to 800°C. That is, precipitates formed by combining Mo with Nb, Ti and V precipitate finely during reheating, for example during temperature rise at a fire, by: adding appropriate amounts of Mo, Nb, Ti and V; keeping a heating temperature high at hot rolling; thus making those elements dissolve sufficiently; also introducing proper structure after hot rolling having a high dislocation density; and, by so doing, securing precipitation sites where precipitates can occur.
• composition of a composite carbonitride precipitates that are important for the securing a high temperature strength can easily be identified by analysis with, for example, an electron microscope or an EDX.
• the amount of a thermodynamically stable precipitates that are formed equilibriously and the amounts of alloying elements that dissolve in a BCC phase can easily be calculated from the amounts of the alloying elements addition by using a commercially available software for a thermodynamic computation database or the like.
• the concept of the present invention is to enhance strengthening at a high temperature by utilizing precipitates and dissolved elements and, thus, the amounts of addition alloying elements, such as Cr, Mn and Mo, that have so far been added abundantly to a conventional steel for high temperature use can rather be restrained at a low level. Therefore, it is possible to design alloy addition so as not to deteriorate weldability.
• a microstructure is made comprising composite structure composed of ferrite and bainite and the bainite fraction is controlled in the range from 20 to 95%. The reason is that an excessive ferrite fraction in a microstructure makes it difficult to secure strength both at room temperature and at a high temperature by increasing the amounts of alloying elements addition.
• % means a percent in terms of mass.
• C is an element that affects the properties of a steel most conspicuously and is essential for the formation of composite precipitates (carbides) with Mo, Nb, Ti and V. Therefore, a C amount of at least 0.005% is necessary. If a C amount is less than the amount, the strength of a steel is insufficient. However, when C is added in excess of 0.08%, the Ac 1 transformation temperature lowers, and therefore strength at 800°C is hardly obtained and toughness also deteriorates. For those reasons, a C amount is limited in the range from 0.005 to 0.08%.
• a C amount is preferable to limit a C amount to less than 0.04% in order to keep the matrix composed of ferrite and bainite thermodynamically stable during high temperature heating corresponding to a fire, to maintain the coherency of the matrix with carbonitride precipitates compositely containing Mo, Nb, V and Ti, and thus secure the strengthening effect.
• Si is an element contained in a steel as a deoxidizing agent and is effective in enhancing the strength of a steel at room temperature as it has a function of strengthening a steel by acting as substitutional solution hardening.
• Si does not have the effect of enhancing strength particularly at a high temperature exceeding 600°C. If Si is added abundantly, weldability and HAZ toughness deteriorate, and therefore the upper limit of an Si amount is limited to 0.5%.
• a steel can be deoxidized only by Ti and/or Al, and therefore it is preferable that an si amount is as low as possible from the viewpoint of HAZ toughness and hardenability. Therefore, Si may not necessarily be added.
• Mn is an element indispensable for securing strength and toughness. Mn is a substitutional solution hardening element and therefore it is effective for the enhancement of strength at room temperature. However, Mn does slight contribution to increase high temperature strength exceeding 600°C. For that reason, in a steel containing a comparatively large amount of Mo, such as a steel according to the present invention, an Mn amount is limited to not more than 1.6% from the viewpoint of the improvement of weldability, namely the lowering of a PCM value. To control the upper limit of a Mn amount to a low level is advantageous also from the viewpoint of the control of the segregation at the center of a continuously cast slab.
• the addition of Mn must be restrained and it is desirable to set the upper limit at 0.9%.
• the lower limit of an Mn amount is not particularly regulated, but it is desirable to add Mn by not less than 0.1% from the viewpoint of the securing of the strength and toughness of a steel.
• a cooling rate must be not lower than 0.3 K/sec. in the temperature range from 800°C to 650°C after the completion of hot rolling. That is, a comparatively thin steel sheet less than about 25 mm in thickness must be produced through an air cooling process or an accelerated cooling (water cooling) process, and a comparatively thick steel sheet more than about 25 mm in thickness must be produced through an accelerated cooling (water cooling) process.
• P is an impurity in a steel according to the present invention and the reduction of a P amount tends to reduce intergranular fracture at a HAZ. Therefore, it is preferable that a P amount is as small as possible.
• a P amount is high, the low temperature toughness of a steel and a weld deteriorate. For that reason, the upper limit of a P amount is set at 0.02%.
• S is an impurity in a steel according to the present invention and therefore it is preferable that an S amount is as small as possible from the viewpoint of the low temperature toughness of a base steel.
• an S amount is high, the low temperature toughness of a base steel and a weld deteriorate. For that reason, the upper limit of an S amount is set at 0.01%.
• Mo is a basic element that constitutes composite precipitates which enhance high temperature strength and thus is an essential element in a steel according to the present invention. It is necessary to add Mo by not less than 0.1% in order to obtain composite precipitates formed by combining Mo with Nb and Ti or composite precipitates formed by combining Mo with Nb, Ti and V at a high density and thus enhance high temperature strength. On the other hand, when Mo is added in excess of 1.5%, the uniformity of the properties of a steel is hardly controlled, the toughness of a weld heat-affected zone deteriorates, and also the economical efficiency is lost. For those reasons, an addition amount of Mo is limited in the range from 0.1 to 1.5%, preferably from 0.2 to 1.1%.
• Nb is an element that contributes important roles in securing strength at a high temperature of 700°C or 800°C in a steel according to the present invention to which a comparatively large amount of Mo is added.
• Nb is an element that is useful for raising the recrystallization temperature of austenite and exhibiting the effect of controlled rolling during hot rolling to the maximum.
• Nb contributes to the grain size refinement of austenite in a heated steel at reheating prior to hot rolling, normalizing or quenching.
• Nb has the effect of enhancing strength by precipitation hardening, and also contributes to the enhancement of high temperature strength by the combined addition with Mo.
• the amount of Nb addition is less than 0.03%, the effect of precipitation hardening is insufficient in the temperature range from 700°C to 800°C, and therefore it is preferable to add Nb by not less than 0.1%.
• an Nb amount exceeds 0.2%, the toughness of a steel may deteriorate, and therefore the upper limit of an Nb amount is set at 0.3%. Consequently, a Nb amount is limited in the range from 0.03 to 0.3%.
• Ti like Nb, is also effective for the enhancement of high temperature strength.
• Ti forms precipitates mainly composed of Ti 2 O 3 by combining with O, the precipitates act as nuclei for forming intragranular transformed ferrite, and that improves toughness at a weld.
• Ti forms TiN in the slab by combining with N, restrains the coarsening of ⁇ grains during reheating, and thus is effective for the microstructure refinement after hot rolling, and further that fine TiN remaining in a steel sheet refines microstructure of a heat-affected zone at welding.
• a Ti amount of at least 0.005% is necessary in order to secure those effects.
• a Ti amount is preferably not more than 0.02%; the upper limit thereof is 0.025%.
• B is very important in controlling strength through the control of the fraction of bainite formed. That is, B is effective in improving hardenability by segregating at the grain boundaries of austenite and restraining ferrite formation, and forming bainite stably even when a cooling rate is comparatively low as in air cooling.
• a B amount of at least 0.0005% is necessary in order to secure the above effects.
• the upper limit of a B amount is set at 0.003%.
• Al is an element generally contained in a steel as a deoxidizing agent. However, only Si or Ti can play the role of deoxidization sufficiently and thus the lower limit of an Al amount is not specified in the present invention (including the case of an Al amount is zero). On the other hand, if an Al amount is excessive, not only the cleanliness of a steel deteriorates but also the toughness of a weld metal deteriorates. Therefore, the upper limit of an Al amount is set at 0.06%.
• N is an element that is contained in a steel as an unavoidable impurity and the lower limit of an N amount is not particularly specified.
• the increase of an N amount is extremely detrimental to toughness at a HAZ and weldability. Therefore, the upper limit thereof is set at 0.006% in a steel according to the present invention.
• Ni enhances the strength and toughness of a steel while weldability and toughness at a HAZ are not badly affected. In order to secure those effects, Ni must be added by at least not less than 0.05%. On the other hand, if Ni is added excessively, not only economical efficiency is harmed but also weldability is adversely affected, and therefore the upper limit of an Ni amount is set at 1.0%.
• Cu exhibits almost the same effects and roles as Ni.
• An excessive addition of Cu causes the deterioration of weldability and the generation of Cu-induced cracks during hot rolling which makes the production difficult, and therefore the upper limit of a Cu amount is set at 1.0%.
• the lower limit of a Cu amount should be the least amount in which a substantial effect is obtained and thus is set at 0.05%.
• Cr enhances both the strength and the toughness of a steel.
• an addition amount of Cr is excessive, the toughness and weldability of both a base steel and a weld are deteriorated, and therefore a Cr amount is limited in the range from 0.05 to 1.0%.
• the aforementioned Cu, Ni and Cr are effective in not only the strength and toughness of a steel but also the weather resistance thereof. For those purposes, it is preferable to add the elements within the range where weldability is not hindered.
• V has almost the same function of composite precipitation as Nb has, but the effect thereof is smaller than that of Nb. Further, V influences hardenability and also contributes to the enhancement of high temperature strength. The same effect as Nb is hardly obtained with a V addition amount of less than 0.01%. On the other hand, if the amount of V addition is excessive, the toughness of a steel deteriorates sometimes. Therefore, the lower and upper limits of a V amount in a steel according to the present invention are set at 0.01% and 0.1%, respectively.
• Ca and REM combine with S, which is an impurity, and have the functions of enhancing toughness and restraining cracks induced by dispersed hydrogen at a weld. However, if their amounts are excessive, coarse inclusions are formed and they exert harmful influence. Therefore, the adequate content of Ca or REM is 0.0005 to 0.004%.
• Mg has the functions of restraining the growth of austenite grains and fractionizing them at a heat-affected zone, and enhances toughness at a weld. In order to secure those effects, a Mg addition of not less than 0.0001% is necessary. On the other hand, if the Mg addition increases, the degree of the effects to the increase of the addition amount decreases and economical efficiency is harmed. Therefore, the upper limit of an Mg amount is set at 0.006%.
• PCM is an index that represents weldability and, as a PCM value decreases, weldability improves. In a steel according to the present invention, an excellent weldability can be secured as long as a PCM value is not more than 0.20%.
• the diameter of prior austenite grains in a finally transformed structure is limited to not larger than 150 ⁇ m in terms of an average circle-equivalent diameter at the position in the depth of one-fourth of the sheet thickness on a cross section in the direction of the final hot rolling of a steel sheet.
• the reason is that a prior austenite grain diameter significantly influences toughness together with a microstructure and it is very important and essential to control the prior austenite grain diameter to as small as possible, particularly in order to enhance the toughness of such a Mo-added steel according to the present invention.
• an average circle-equivalent diameter can be obtained by: using a notched impact test piece with that is cut out from a position the center of which is in the depth of one-fourth of the sheet thickness in a direction perpendicular to the final hot rolling direction of a steel sheet, for example a JIS Z2202 No. 4 test piece (with 2 mm V-notch); defining a unit of fractured faces caused by the brittle fracture of the test piece at a sufficiently low temperature as an effective grain diameter that can be regarded as a prior austenite grain diameter; and measuring the average circle-equivalent diameter of the units.
• the value must be not larger than 150 ⁇ m.
• a reheating temperature is high when a slab or an ingot is rolled in order to sufficiently dissolve Mo, Nb, Ti and v.
• the reheating temperature is limited in the range from 1,100°C to 1,250°C from the viewpoint of the securement of the toughness of a steel.
• the reheated slab or ingot is subjected to hot rolling while an cumulative reduction ratio of not less than 30% relative to the finish-rolled sheet thickness is secured in a temperature range of not higher than 1,100°C, and then the hot rolling is completed at a temperature not lower than 850°C.
• reduction in a low temperature range is excessive, ferrite transformation is accelerated, a ferrite fraction becomes excessive, thus strength is hardly secured, further Nb, Ti and V precipitate as carbides during the hot rolling, and thus necessary amounts of dissolved Mo, Nb, Ti and V are not obtained.
• the lower limit of a hot rolling finishing temperature is 850°C.
• the upper limit of a hot rolling finishing temperature is set at 1,100°C.
• the resultant steel sheet is cooled at an average cooling rate of not less than 0.3 K/sec., which is measured on the surface of the steel sheet, in the temperature range from not lower than 800°C to not higher than 650°C in terms of the temperature of the steel sheet surface.
• the object is to obtain a microstructure, after hot rolling, that abundantly contains deformation bands and dislocations acting as the sites of precipitation, and then, by freezing those with water cooling, to obtain composite precipitates at a high density, the composite precipitates being formed by combining Mo with Nb, Ti and V and, during reheating, being kept fine and coherent to the matrix.
• a steel sheet may be subjected to tempering treatment in a temperature of not higher than 500°C for not longer than 30 minutes after water cooling.
• a steel according to the present invention can sufficiently enjoy the advantages even when it is used in the form of such a steel as a heavy steel plate, a steel pipe, a steel sheet, a section steel or the like.
• Steel sheets (15 to 50 mm in thickness) having various steel components were produced through the processes of a converter, continuous casting and plate rolling, and the strength, toughness, yield strength at 700°C and 800°C, occurrence of root cracks during the y-crack test without preheating (at room temperature) and the like of the resultant steel sheets were investigated.
• steels Nos. 1 to 9 all the microstructures comprising the composite structures composed of ferrite and bainite and the average circle-equivalent diameters of prior austenite grains were not larger than 120 ⁇ m. Thus obtained yield strength ratios were excellent; 64% and 23% at 700°C and 800°C, respectively.
• each of the microstructures comprising a single structure composed of bainite or a composite structure composed of ferrite and bainite and the average circle-equivalent diameters of prior austenite grains were not larger than 120 ⁇ m.
• yield strength ratios were excellent; 61% and 25% at 700°C and 800°C, respectively.
• the C amount was insufficient
• the yield strength was insufficient as a steel of 490 MPa class
• the amount of the composite carbonitrides formed in the high temperature of not lower than 600°C was less than 5 x 10 -4
• the ratio (p) of the yield strength at the high temperature to that at room temperature was less than the value defined by the expression -0.0029 x T + 2.48.
• the Mn amount exceeds 1.6%, therefore the Ac 1 temperature was lower than 800°C, and the ratio (p) of the yield strength at the high temperature to that at room temperature is less than the value defined by the expression -0.0029 x T + 2.48 in the temperature range of not lower than 700°C.
• the Mn amount was less than 0.1%, therefore the effect of solution hardening was insufficient at room temperature, and thus the yield strength and the tensile strength at room temperature were lower than the relevant lower limits of the standard values of a 490 MPa class steel.
• the S amount exceeds 0.01%, and therefore both the ductile-brittle transition temperature of the base steel and the absorbed energy of the reproduced HAZ at 0°C deteriorated, similarly to the comparative steel No. 23.
• the reheating temperature was lower than 1,100°C, and therefore the added alloying elements did not dissolve in austenite during the reheating, a sufficient precipitation hardening effect was not obtained, and the ratio (p) of the yield strength at the high temperature to that at room temperature was less than the value defined by the expression -0.0029 x T + 2.48, though both the yield strength and the tensile strength at room temperature were good.
• the reheating temperature was as high as 1,250°C, and therefore the austenite grains after the completion of the hot rolling were coarse; larger than 120 ⁇ m, and the toughness of the base steel was low.
• the sheet thickness was thicker than 25 mm, and therefore it was attempted to secure a cooling rate of not less than 0.3 K/sec. by applying accelerated cooling.
• the temperature at the start of water cooling was lower than 700°C
• the cooling rate during the time period from the completion of the hot rolling to the start of the cooling (at 690°C) is less than 0.3 K/sec.
• the transformation of ferrite proceeds before the start of the water cooling.
• the bainite fraction was less than 20% and the tensile strength at room temperature was lower than 490 MPa.
• a steel that has a specific chemical components and is produced by a method according to the present invention has a microstructure comprising a composite structure composed of ferrite and bainite or a single structure composed of bainite; is a high-tensile-strength steel having a strength of not lower than 490 MPa at room temperature; has the feature of satisfying the expression p ⁇ -0.0029 x T + 2.48 when the steel material temperature T (°C) is in the temperature range from 600°C to 800°C, wherein p is the ratio of a stress at a high temperature to that at room temperature (a yield stress at a high temperature/ a yield stress at room temperature); thus has the properties required of a fire-resistant steel for building construction; and is an entirely novel steel with qualities beyond those of all previous steels.

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• 2003
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