JP4515427B2 - Steel with excellent toughness and fatigue crack growth resistance in weld heat affected zone and its manufacturing method - Google Patents

Description

  The present invention repeats the toughness of a portion affected by heat (hereinafter, also referred to as “welding heat affected zone” or “HAZ”) when welding steel materials used in bridges, high-rise buildings, ships, etc., and repeatedly The present invention relates to a steel material with improved fatigue crack propagation resistance under stress and a method for producing the same.

  The properties required for steel materials used in bridges, high-rise buildings, ships and the like have become increasingly severe in recent years, and particularly good toughness is required. In general, these steel materials are often joined by welding. In particular, HAZ has a problem that the toughness is easily deteriorated due to thermal influence during welding. This deterioration in toughness becomes more noticeable as the heat input during welding increases, and the cause is that the larger the heat input during welding, the slower the cooling rate of the HAZ, the lower the hardenability and the formation of coarse island martensite. It is thought that there is to do. Therefore, in order to improve the toughness of the HAZ, it is considered that the heat input during welding should be suppressed as much as possible. However, in order to increase the welding work efficiency, for example, the heat input of welding such as electrogas welding, electroslag welding, submerged welding, etc. It is desired to adopt a high heat input welding method of 40 kJ / mm or more.

  Several steel materials that suppress the HAZ toughness deterioration when the high heat input welding method is adopted have already been proposed. For example, Patent Document 1 discloses a steel material in which fine TiN is dispersed and reprecipitated in the steel material to suppress coarsening of austenite grains generated in the HAZ when high heat input welding is performed, and deterioration in HAZ toughness is suppressed. Has been proposed. However, as a result of investigations by the present inventors, when the weld metal becomes a high temperature of 1400 ° C. or higher, the TiN is dissolved in the HAZ by the heat received during welding, particularly in a portion (bond portion) close to the weld metal. Therefore, it has been found that the deterioration of the HAZ toughness cannot be sufficiently suppressed.

  Patent Document 2 discloses controlling the form of oxides and nitrides contained in steel as a technique for improving the toughness of the base material and the HAZ. In this document, Ti and Zr are used in combination to produce fine oxides and nitrides to improve the toughness of the matrix and HAZ, and to produce such fine oxides and nitrides. It is disclosed that Ti and Zr may be added in this order in the manufacturing process. However, as a result of investigations by the present inventors, it is only necessary to increase the amount of oxide in order to further increase the toughness of HAZ. However, in the technique of Patent Document 2 described above, if a large amount of Ti or Zr is added to increase the amount of oxide, It turned out that carbide | carbonized_materials, such as Ti and Zr, are formed and the toughness of steel materials (base material) falls on the contrary.

The present inventors have previously proposed a steel material in which the toughness of the HAZ does not deteriorate even in the case of being affected by high temperature heat during welding. This steel material is composed of complex oxides such as La ₂ O ₃ —SiO ₂ oxide, Ce ₂ O ₃ —SiO ₂ oxide, and La ₂ O ₃ —Ce ₂ O ₃ —SiO ₂ oxide in the steel material. This composite oxide is in a liquid state in molten steel, so it is finely dispersed in the steel, and it does not disappear in solid solution even if it is affected by heat at the time of welding. This contributes to improving the toughness of HAZ. . Patent Document 3 discloses that in order to generate the composite oxide, La and Ce are added to the molten steel whose dissolved oxygen content is adjusted, and then Si is added. Further, Patent Document 3 describes that the toughness of HAZ can be further enhanced by adding Ti to the steel material and precipitating TiN in the steel material structure, and in order to generate such TiN, the composite oxide is generated. It is also disclosed that Ti may be added to the molten steel.

  By the way, since there are many cases where the above various structural materials are repeatedly stressed, in order to ensure the safety of the structural materials, not only the HAZ toughness but also the steel material has good fatigue characteristics in the design. Very important.

  The fatigue process of steel materials can be broadly divided into two processes, namely, the generation of cracks in stress-concentrated portions and the progress of cracks once generated. In general machine parts, the occurrence of macroscopic cracks is considered as a use limit, and there is almost no design that allows the cracks to propagate. However, in a welded structure, even if a fatigue crack occurs, it does not immediately break, and before this crack reaches the final stage, it is discovered by periodic inspection etc., and the cracked part is repaired, Or if the crack does not grow to the length that will lead to final failure within the period of use, the structure will be able to withstand sufficient use even if there is a crack.

  In welded structures, there are many weld toes as stress-concentrated parts, and it is almost impossible technically and economically to completely prevent the occurrence of fatigue cracks. Absent. That is, in order to improve the fatigue life of the welded structure, it is effective to significantly extend the crack propagation life from the state in which the crack already exists, rather than preventing the occurrence of the crack itself. For that purpose, the design which makes the progress rate of the crack of steel materials as slow as possible becomes an important matter.

Various techniques have been proposed so far to suppress the fatigue crack growth rate and increase the fatigue crack growth resistance. For example, Patent Document 4 discloses a two-phase structure of a hard phase and a soft phase, and a soft phase. / Techniques have been proposed that suppress the crack growth rate by bending, retaining, and branching cracks at the hard phase boundary. However, this technology does not consider the improvement of the HAZ toughness of the welded part, and in order to further improve the safety, it is desired to realize a steel material excellent in the toughness of the welded heat affected zone and the fatigue crack growth resistance. ing.
Japanese Patent Publication No.55-26164 JP 2003-213366 A JP 2005-48265 A Japanese Patent No. 3298544

  The present invention has been made in view of the above circumstances, and its purpose is to suppress HAZ toughness especially when welding with a heat input of 40 kJ / mm or more and to suppress the fatigue crack growth rate under repeated stress. It is another object of the present invention to provide a steel material with improved fatigue crack growth resistance and a method for producing the same.

That is, the steel material according to the present invention that has solved the above problems is
C: 0.03 to 0.18% (meaning “mass%”; the same shall apply hereinafter)
Si: 0.5% or less (excluding 0%),
Mn: 0.9-2.0%, and N: 0.003-0.01%,
P: 0.02% or less (excluding 0%),
S: 0.015% or less (not including 0%) and Al: 0.01% or less (not including 0%),
REM: 0.001-0.1% and / or Ca: 0.0003-0.02%,
Zr: 0.001 to 0.05% each contained,
The balance is steel consisting of iron and inevitable impurities,
REM and / or Ca and Zr as a single oxide or composite oxide, and a composite structure composed of a soft phase and a hard phase, and Vickers hardness Hv _{1 of the} hard phase and Vickers hardness of the soft phase is Hv ratio of ₂ (Hv ₁ / Hv ₂₎ is 1.5 to 5.0, with the gist in that the particle size of the soft phase is 20μm or less in circle equivalent diameter.

The steel material has a total REM oxide and / or CaO content of 5% or more and a ZrO ₂ content of 5% when the composition of all oxides contained in the steel material is measured and converted to mass as a single oxide. It is preferable to satisfy the above.

  It is preferable that the steel material further contains Ti: 0.08% or less (not including 0%) as another element and also contains the Ti as a single oxide or a composite oxide. It is because the toughness of the weld heat affected zone can be further improved by including Ti. As described above, when the steel material contains Ti, it is preferably 0.3% or more when the composition of all oxides contained in the steel material is measured and converted into mass as a single oxide.

The steel material, as another element,
Cu: 2% or less (excluding 0%),
Ni: 3.5% or less (excluding 0%),
Cr: 3% or less (excluding 0%),
Mo: 1% or less (excluding 0%),
Nb: 0.25% or less (excluding 0%),
V: 0.1% or less (not including 0%), and B: 0.005% or less (not including 0%)
Those containing one or more elements selected from the group consisting of these elements are preferred, and the strength of the base material can be increased by containing these elements.

  In the steel material of the present invention, the soft phase is at least one selected from the group consisting of ferrite, tempered bainite and tempered martensite, and the hard phase includes bainite and / or martensite (including island martensite). It is done.

  The steel material according to the present invention can be manufactured, for example, by adding at least one element selected from the group consisting of REM and Ca and Zr to molten steel whose dissolved oxygen content is adjusted to a range of 0.0020 to 0.010%. . When the steel material contains Ti in particular, at least one element selected from the group consisting of REM and Ca, Ti, and Zr to a molten steel whose dissolved oxygen content is adjusted to a range of 0.0020 to 0.010%. Is preferably added. In this case, it is preferable to add Ti prior to adding at least one element selected from the group consisting of REM and Ca and Zr to the molten steel in which the amount of dissolved oxygen is adjusted.

According to the present invention, in order to disperse, in the steel material, an oxide having a composition that does not dissolve in the steel material even when reaching a high temperature of 1400 ° C. in the high heat input welding, it is not limited to small to medium heat input welding. Even in heat input welding, it is possible to prevent toughness deterioration of the weld heat affected zone (HAZ). Further, the steel structure is a composite structure composed of a soft phase and a hard phase, and the ratio (Hv ₁ / Hv ₂ ) between the Vickers hardness Hv _{1 of the} hard phase and the Vickers hardness Hv ₂ of the soft phase is within a predetermined range. In addition to reducing the particle size of the soft phase, the steel material was also excellent in fatigue crack growth resistance.

The present inventors first studied whether or not improvement in HAZ toughness could be achieved by dispersing an oxide having a composition different from that of Patent Document 3 in the steel material in order to increase the toughness of HAZ. As a result, if REM and / or Ca and Zr are combined and added to the steel, and the REM and / or Ca and Zr are adjusted to be contained in the steel as a single oxide or a composite oxide, the welding heat It is possible to increase the toughness of the affected zone, and to further improve the HAZ toughness by adjusting to contain Ti as a single oxide or composite oxide by further adding Ti to such a component system. I found it. Further, in order to increase the fatigue crack propagation resistance of the steel material without hindering the improvement of the HAZ toughness due to the oxide, the ratio of the Vickers hardness Hv _{1 of the} hard phase to the Vickers hardness Hv ₂ of the soft phase (Hv ₁ / Hv ₂ ) is controlled to be within a predetermined range, and when the particle size of the soft phase is made finer, the properties are improved, and the present invention has been completed. Hereinafter, the present invention will be described in detail.

  First, the steel material of the present invention contains REM and / or Ca and Zr as a single oxide or a composite oxide. If such an oxide is included, the oxide does not disappear in a solid solution even at a high temperature of 1400 ° C. due to the heat effect during welding, so the austenite grains are coarsened in the HAZ during welding. As a result, the HAZ toughness can be further improved as compared with the case where REM, Ca, and Zr are added individually to form an oxide.

  And if it combines in the steel materials combining the said single oxide or composite oxide, the absolute amount of all the oxides contained in steel materials can be increased, and it will cause toughness deterioration of steel materials (base materials). Generation of REM sulfide, Ca sulfide, or Zr carbide can be prevented, and as a result, HAZ toughness can be improved while suppressing toughness deterioration of the base material.

The steel material of the present invention contains (a) an oxide of REM and / or CaO and ZrO ₂ , or (b) a composite oxide containing REM and / or Ca and Zr, or (c ) Any oxide containing REM and / or CaO and ZrO ₂ and any composite oxide containing REM and / or Ca and Zr may be used. Examples of the composite oxide containing REM and / or Ca and Zr include a composite oxide containing REM and Zr, a composite oxide containing Ca and Zr, and a composite oxide containing REM, Ca, and Zr.

The steel material of the present invention preferably further contains an oxide of Ti in addition to the oxides described above. That is, any composition may be used as long as it contains Ti ₂ O ₃ , Ti ₃ O ₅ , or TiO ₂ when the composition of all oxides contained in the steel material is measured and converted into mass as a single oxide. By containing the oxide of Ti, the amount of oxide dispersed in the steel material can be further increased, so that the HAZ toughness can be further improved.

The Ti oxide may be contained in the steel material as a single oxide (Ti ₂ O ₃ , Ti ₃ O ₅ , TiO ₂ ) or, for example, the composite oxide (that is, a composite containing REM and Zr). Oxide, composite oxide containing Ca and Zr, composite oxide containing REM, Ca and Zr), and may be contained as a composite oxide.

When the composition of all oxides contained in the steel material is measured and converted into mass as a single oxide, the total amount of oxides of REM and / or CaO is 5% or more, and the steel material occupies the total oxides. It is preferable that ZrO ₂ satisfies 5% or more. The reason is to ensure the amount of oxide that contributes to the improvement of HAZ toughness. The total of REM oxides and / or CaO is preferably 10% or more, more preferably 15% or more, and still more preferably 20% or more. On the other hand, ZrO ₂ is preferably 10% or more, more preferably 15% or more, and further preferably 20% or more.

When the steel material contains an oxide of Ti, the composition of all oxides contained in the steel material is measured, and when converted to mass as a single oxide, the oxide of Ti satisfies 0.3% or more. It is preferable. More preferably, it is 1% or more, more preferably 3% or more, particularly preferably 5% or more, and most preferably 10% or more. The Ti oxide exists in the steel as Ti ₂ O ₃ , Ti ₃ O ₅ , TiO ₂ , but the composition of all oxides contained in the steel is measured, and all Ti oxides are converted into Ti ₂ value converted as O ₃ has only to satisfy the above range.

The steel material of the present invention is a REM oxide and / or CaO and a ZrO ₂ and Ti oxide (Ti ₂ ) when the composition of all oxides contained in the steel material is measured and converted into mass as a single oxide. The total (O ₃ conversion) is preferably 55% or more. This is because if the total of these oxides is less than 55%, the amount of oxide contributing to the improvement of HAZ toughness is insufficient, and the HAZ toughness cannot be sufficiently improved. More preferably, it is 60% or more, More preferably, it is 65% or more.

The remaining components of the total oxide composition are not particularly limited, but may be, for example, SiO ₂ , Al ₂ O ₃ , or MnO when converted as a single oxide. It is preferable to keep the “other” components other than SiO ₂ , Al ₂ O ₃ and MnO to less than 5%.

The composition of the oxide contained in the steel material is determined by observing the cross section of the steel material with, for example, EPMA (Electron Probe X-ray Micro Analyzer) and quantitatively analyzing the inclusions observed in the observation field. Can be measured. In the observation of EPMA, for example, the acceleration voltage is 20 kV, the sample current is 0.01 μA, the observation visual field area is 1 to 5 cm ^2, and the composition at the center of the inclusion is quantitatively analyzed by wavelength dispersion spectroscopy of characteristic X-rays.

  The size of inclusions to be analyzed is a maximum diameter of 0.2 μm or more, and the number of analyzes is at least 100.

  The analysis target elements are Al, Mn, Si, Ti, Zr, Ca, La, Ce, and O. Using a known substance, the relationship between the X-ray intensity and the element concentration of each element is obtained in advance as a calibration curve. From the X-ray intensity obtained from the inclusions to be measured and the calibration curve, the element concentration contained in the inclusions to be analyzed is quantified, and inclusions having an oxygen content of 5% or more are defined as oxides. However, when a plurality of elements are observed from one inclusion, the composition of the oxide is calculated in terms of a single oxide of each element from the ratio of X-ray intensity indicating the presence of these elements. In the steel material of the present invention, the average of the quantitative results thus obtained for the individual oxides is taken as the average composition of the oxides.

  Next, the component composition in the steel material (base material) of the present invention will be described. The steel material of the present invention is characterized in that it contains REM: 0.001 to 0.1% and / or Ca: 0.0003 to 0.02% and Zr: 0.001 to 0.05%. The reasons for setting these ranges are as follows.

REM, Ca, and Zr are REM single oxide, Ca single oxide (CaO), Zr single oxide (ZrO ₂ ), or a composite oxide of REM and / or Ca and Zr. It is an element that forms and contributes to the improvement of HAZ toughness. In the steel material of the present invention, REM and Ca may be used alone or in combination.

  When REM is contained, it should be 0.001% or more, preferably 0.006% or more, more preferably 0.010% or more. However, if added excessively, sulfide of REM is generated and the toughness of the base material deteriorates, so it should be suppressed to 0.1% or less. Preferably it is 0.09% or less, More preferably, it is 0.08% or less. In the present invention, REM (rare earth element) means a lanthanoid element (15 elements from La to Ln) and Sc (scandium) and Y (yttrium). Among these elements, La, Ce It is preferable to contain at least one element selected from the group consisting of Y and Y, more preferably La and / or Ce.

  When Ca is contained, it should be 0.0003% or more, preferably 0.0005% or more, more preferably 0.0008% or more. However, if excessively added, coarse Ca sulfide is generated and the toughness of the base material deteriorates, so it should be suppressed to 0.02% or less. Preferably it is 0.015% or less, More preferably, you may be 0.01% or less.

  Zr should be contained in an amount of 0.001% or more, preferably 0.003% or more, and more preferably 0.005% or more. However, if added excessively, coarse Zr carbide is generated and the toughness of the base material deteriorates, so it should be suppressed to 0.05% or less. Preferably it is 0.04% or less, More preferably, it is 0.03% or less.

  The steel material of the present invention includes REM and / or Ca and Zr, and as basic elements, C: 0.03 to 0.18%, Si: 0.5% or less (not including 0%), Mn: It contains 0.9 to 2.0% and N: 0.003 to 0.01%. The reason for setting such a range is as follows.

  C is an element indispensable for securing the strength of a steel material (base material), and in order to exert such effects, it is necessary to contain 0.03% or more. Preferably it is 0.04% or more, More preferably, it is 0.05% or more. However, if it exceeds 0.18%, a lot of island martensite is generated in the HAZ at the time of welding and not only causes deterioration of the toughness of the HAZ, but also adversely affects the weldability. Therefore, C should be suppressed to 0.18% or less, preferably 0.15% or less.

  Si is an element that has a deoxidizing action and contributes to improving the strength of the steel (base material). In order to exhibit such an effect effectively, it is preferable to contain 0.02% or more, more preferably 0.05% or more, and still more preferably 0.1% or more. However, if it exceeds 0.5%, the weldability and base material toughness of the steel (base material) deteriorate, so it is necessary to keep it to 0.5% or less. Preferably it is 0.45% or less, More preferably, it restrains to 0.4% or less. In addition, when the further high toughness of HAZ is calculated | required, it is good to suppress Si to 0.3% or less.

  Mn is an element that contributes to improving the strength of the steel material (base material), and in order to exert such an effect effectively, it is necessary to contain 0.9% or more. Preferably it is 1.0% or more. However, since the HAZ toughness deteriorates when the content exceeds 2.0%, the Mn content is set to 2.0% or less. Preferably it is 1.70% or less.

  N is an element that precipitates nitrides (for example, ZrN and TiN), and the nitrides prevent austenite grains formed in the HAZ during welding and promote ferrite transformation, so that the toughness of the HAZ is increased. Contributes to improvement. In order to exhibit such an effect effectively, it is contained 0.003% or more. Preferably it is 0.004% or more. The more N, the more refined austenite grains are promoted, which effectively works to improve the toughness of HAZ. However, if it exceeds 0.01%, the amount of solute N increases and the toughness of the base material deteriorates. Therefore, N must be suppressed to 0.01% or less, preferably 0.009% or less, more preferably 0.008% or less.

  The steel material of the present invention contains the above elements, P: 0.02% or less (not including 0%), S: 0.015% or less (not including 0%), and Al: 0.01% or less ( 0% is not included). The reason for setting such a range is as follows.

  P is an element that easily segregates, and particularly segregates at a grain boundary in the steel material to deteriorate toughness. Therefore, P must be suppressed to 0.02% or less, preferably 0.018% or less, more preferably 0.015% or less.

  S is a harmful element that combines with Mn to produce sulfide (MnS) and degrades the toughness of the base material and the ductility in the thickness direction. S combines with La and Ce to form LaS and CeS and inhibits the formation of oxides. Therefore, S should be suppressed to 0.015% or less, preferably 0.012% or less, more preferably 0.008% or less, and particularly 0.006% or less.

  Al is an element having a strong deoxidizing power, and when added in excess, the oxide is reduced and it becomes difficult to produce a desired oxide. Therefore, Al must be suppressed to 0.01% or less, preferably 0.0090% or less, more preferably 0.0080% or less.

  The contained elements defined in the present invention are as described above, and the balance is iron and unavoidable impurities, and as the unavoidable impurities, elements brought in depending on the situation of raw materials, materials, production facilities, etc. (for example, Mg and As , Se, etc.) can be permitted. Further, it is possible to further contain the following elements.

<Ti: 0.08% or less (excluding 0%)>
Ti is an element that contributes to improving the toughness of HAZ by generating an oxide of Ti in the steel material. In order to exert such an effect effectively, Ti is preferably contained in an amount of 0.005% or more, more preferably 0.007% or more, and further preferably 0.01% or more. However, if added excessively, a large amount of oxide is generated and the toughness of the steel (base material) is deteriorated, so it should be suppressed to 0.08% or less. Preferably it is 0.07% or less, More preferably, it is 0.06% or less.

  In order to increase the strength of the steel material of the present invention, Cu: 2% or less (excluding 0%), Ni: 3.5% or less (not including 0%), Cr: 3% or less (0% Mo: 1% or less (not including 0%), Nb: 0.25% or less (not including 0%), V: 0.1% or less (not including 0%), and B: 0 It is also effective to contain one or more elements selected from the group consisting of 0.005% or less (not including 0%). The reasons for setting these ranges are as follows.

<Cu: 2% or less (excluding 0%)>
Cu is an element for solid solution strengthening of the steel material, and in order to exhibit such an effect effectively, it is preferable to contain 0.05% or more. More preferably, it is 0.1% or more, More preferably, it is 0.2% or more. In particular, when 0.6% or more is contained, in addition to solid solution strengthening, aging precipitation strengthening is also exhibited, and a significant improvement in strength becomes possible. However, if the content exceeds 2%, the toughness of the steel material (base material) decreases, so Cu should be suppressed to 2% or less. Preferably it is 1.8% or less, More preferably, you may be 1.6% or less.

<Ni: 3.5% or less (excluding 0%)>
Ni is an element that effectively acts to increase the strength of the steel material and improve the toughness of the steel material. In order to exert such an effect, Ni is preferably contained in an amount of 0.05% or more. More preferably, it is 0.1% or more, More preferably, it is 0.2% or more. The more Ni, the better. However, since it is an expensive element, it is preferable to suppress it to 3.5% or less from an economical viewpoint. More preferably, it is 3.3% or less, More preferably, it is 3% or less.

<Cr: 3% or less (excluding 0%)>
In order to increase the strength by adding Cr, the content is preferably 0.01% or more. More preferably it is 0.02% or more, and still more preferably 0.03% or more. However, if it exceeds 3%, weldability deteriorates, so Cr is preferably suppressed to 3% or less. More preferably, it is 1.5% or less, More preferably, it is 1% or less.

<Mo: 1% or less (excluding 0%)>
In order to increase the strength by adding Mo, it is desirable to contain 0.01% or more. More preferably it is 0.02% or more, and still more preferably 0.03% or more. However, if it exceeds 1%, the weldability deteriorates, so Mo is preferably 1% or less. More preferably, it is 0.9% or less, and more preferably 0.8% or less.

<Nb: 0.25% or less (excluding 0%)>
In order to increase the strength by adding Nb, it is preferable to contain 0.005% or more. More preferably, it is 0.01% or more, More preferably, it is 0.03% or more. However, if it exceeds 0.25%, carbide (NbC) precipitates and the base material toughness deteriorates, so Nb is preferably suppressed to 0.25% or less. More preferably, it is 0.23% or less, and still more preferably 0.20% or less.

<V: 0.1% or less (excluding 0%)>
In order to increase the strength by adding V, it is desirable to contain 0.005% or more. More preferably 0.01% or more, still more preferably 0.03% or more. However, if it exceeds 0.1%, the weldability deteriorates and the toughness of the base material deteriorates. Therefore, V is preferably 0.1% or less. More preferably, it is 0.08% or less, and more preferably 0.06% or less.

<B: 0.005% or less (excluding 0%)>
B increases the strength of the steel material and, in the process of cooling the HAZ heated during welding, combines with N in the steel to precipitate BN and promote ferrite transformation from within the austenite grains. In order to exhibit such an effect effectively, it is preferable to contain 0.0003% or more. More preferably, it is 0.0005% or more, More preferably, it is 0.0008% or more. However, if it exceeds 0.005%, the toughness of the steel (base material) deteriorates, so B is preferably 0.005% or less. More preferably, it is 0.004% or less, and further preferably 0.003% or less.

On the other hand, fatigue cracks proceed in a direction perpendicular to the stress in a normal stable growth region. In order to increase the resistance to crack propagation in consideration of such a fatigue crack propagation mechanism, the steel structure is made into a composite structure, and by detouring (bending) the crack at the boundary between the soft phase and the hard phase, The idea is that the crack growth rate can be reduced and the fatigue life can be extended. A certain hardness difference is required for bending of cracks in the hard phase (hereinafter sometimes referred to as “second phase”). However, if the difference in hardness becomes too large, the hard phase causes brittle fracture, and the crack propagates in the hard phase, so that the effect is reduced. From such a viewpoint, in the steel material of the present invention, the ratio (Hv ₁ / Hv ₂ ) between the Vickers hardness Hv _{1 of the} hard phase and the Vickers hardness Hv ₂ of the soft phase is controlled within a range of 1.5 to 5.0. There is a need to.

That is, by setting the ratio (Hv ₁ / Hv ₂ ) to 1.5 or more, the plastic zone at the interface crack tip between the soft phase and the hard phase changes at the time of dislocation movement at the crack tip, and bending, retention Since branching occurs, the crack growth rate is reduced. However, if the hardness of the hard phase becomes too high, as described above, the hard phase will cause brittle fracture due to the stress at the crack tip, and the effect of suppressing crack propagation will be reduced, so the ratio (Hv ₁ / The value of Hv ₂ ) needs to be 5.0 or less. The preferable lower limit of the value of this ratio is 1.7, more preferably 2.0 or more, and the preferable upper limit is 4.5, more preferably 4.0 or less. In order to control the value of the ratio (Hv ₁ / Hv ₂ ) as described above, it is preferable to appropriately control the ratio of the hard phase and the soft phase. From this viewpoint, the ratio of the soft phase is 20 to 90 area%. It is preferable to do this. In the following, the ratio (Hv ₁ / Hv ₂ ) may be referred to as “hardness ratio”.

  The soft phase in the steel material of the present invention includes at least one selected from the group consisting of ferrite, tempered bainite and tempered martensite, and the hard phase includes bainite and / or martensite (including island martensite). Can be mentioned. Moreover, the structure of the steel material of the present invention may be any structure as long as it includes a soft phase as the first phase and a hard phase as the second phase, but does not necessarily have a two-phase structure. Or the composite structure containing 4 or more types may be sufficient. However, pearlite is a microscopic structure in which soft ferrite and hard cementite that easily brittlely breaks are present in stripes, and the above effect is difficult to obtain, so it is not included in any phase. From such a viewpoint, it is preferable that pearlite is 5 area% or less.

  In addition to the hard phase / soft phase boundary described above, crack growth causes bending, retention, and branching at grain boundaries, thereby reducing the crack growth rate. When the particle size of the soft phase becomes coarse, the frequency of collision with the grain boundary that becomes the resistance to crack propagation decreases, so the crack growth rate does not decrease. In the steel material of the present invention, for example, by carrying out supercooling, the nucleation sites increase and the hard phase is finely dispersed as the ferrite becomes finer. As a result, the probability of encountering the hard phase when the crack progresses is averaged, and the frequency of encounter is increased, so that the effect of decreasing the crack growth rate is obtained. From such a viewpoint, in the steel material of the present invention, it is also necessary that the soft phase has a diameter equivalent to a circle of 20 μm or less (a method for measuring the particle size will be described later). The particle size of the soft phase is preferably 15 μm or less.

  Next, a production method that can be suitably employed in producing the steel material of the present invention will be described. As described above, in order to contain an appropriate amount of REM and / or Ca and Zr as a single oxide or a composite oxide in a steel material, as is apparent from the examples described later, the material is selected from the group consisting of REM and Ca. At least one element selected from the group consisting of REM and Ca to appropriately control the amount of dissolved oxygen immediately before adding Zr, that is, to a molten steel in which the amount of dissolved oxygen is appropriately controlled It is very effective to add Zr in combination. If manufactured by this method, the oxide can be formed reliably even if the amount of REM, Ca, or Zr added is increased to some extent, and as a result, REM sulfide, Ca sulfide, or Zr carbide can be formed. This is because generation can be prevented.

At this time, if the amount of dissolved oxygen is less than 0.0020%, even if Zr is added in combination with at least one element selected from the group consisting of REM and Ca, the amount of oxygen becomes insufficient, so the HAZ toughness is improved. REM or Ca, which could not secure the amount of contributing oxides and could not form oxides, formed sulfides, or Zr formed carbides, deteriorating the toughness of the base material. The amount of dissolved oxygen before adding the above elements is preferably adjusted to 0.0025% or more, and more preferably 0.0030% or more. However, if the amount of dissolved oxygen exceeds 0.010%, the amount of oxygen in the molten steel is too large, and the reaction between the oxygen in the molten steel and the above elements becomes violent, which is not preferable for melting work. Oxides, Ca oxides, and ZrO ₂ are formed. Therefore, the amount of dissolved oxygen should be suppressed to 0.010% or less, preferably 0.008% or less, more preferably 0.007% or less.

  After at least one element selected from the group consisting of REM and Ca and Zr are added in combination, an alloy element may be added to adjust the components of the steel material.

  In addition, when adding the said element to the molten steel which adjusted the amount of dissolved oxygen, what is necessary is just to add at least 1 sort (s) of elements selected from the group which consists of REM and Ca, and Zr, for example, REM and Ca are added together. In order to do this, (a) after adding REM, Ca, and Zr to the molten steel in which the amount of dissolved oxygen is adjusted, the alloy elements may be added to adjust the components of the steel material, and (b) the amount of dissolved oxygen is adjusted. After adding REM (or Ca) and Zr to the adjusted molten steel, an alloy element other than Ca (or REM) may be added to adjust the components of the steel material, and then Ca (or REM) may be added.

  The procedure for adding at least one element selected from the group consisting of REM and Ca and Zr to the molten steel with adjusted dissolved oxygen content is not particularly limited. For example, (a) from the group consisting of REM and Ca After adding at least one element selected, Zr may be added. (B) After adding Zr, at least one element selected from the group consisting of REM and Ca may be added. (C) At least one element selected from the group consisting of REM and Ca and Zr may be simultaneously added in combination. When REM and Ca are added in combination, (d) REM (or Ca) may be added, then Zr may be added, and then Ca (or REM) may be added. (E) REM and Ca Zr may be combined and added simultaneously.

  When the steel material of the present invention contains Ti, after adding Zr in combination with at least one element selected from the group consisting of REM and Ca to the molten steel in which the amount of dissolved oxygen is adjusted, (a) component adjustment of the steel material In addition, Ti may be added together, or (b) after adjusting the components of the steel material, Ti may be added. Preferably, at least one element selected from the group consisting of REM and Ca, and Ti and Zr are added to the molten steel in which the amount of dissolved oxygen is adjusted.

When the steel material contains Ti, it is recommended to add Ti prior to adding at least one element selected from the group consisting of REM and Ca and Zr to the molten steel in which the amount of dissolved oxygen is adjusted. If Ti is added to the molten steel with the dissolved oxygen content adjusted, Ti ₂ O ₃ is first formed, but this Ti ₂ O ₃ has a small interfacial energy with the molten steel, so the size of the formed Ti ₂ O ₃ Becomes fine. Then, by adding Zr in combination with at least one element selected from the group consisting of REM and Ca, the REM oxide, CaO, and ZrO ₂ grow using the Ti ₂ O ₃ as a production nucleus. In addition, the number of particles increases, and the effect of suppressing the coarsening of austenite grains in the HAZ during welding increases.

  By the way, the amount of dissolved oxygen in molten steel primarily refined in a converter or electric furnace usually exceeds 0.010%. Therefore, in the manufacturing method of the present invention, the amount of dissolved oxygen in the molten steel is adjusted to the above range before adding Zr in combination with at least one element selected from the group consisting of REM and Ca, or before adding Ti. There is a need. Examples of the method for adjusting the amount of dissolved oxygen include a method of vacuum C deoxidation using an RH type degassing refining device, a method of adding a deacidifying element such as Si, Mn, Ti, Al, etc. The amount of dissolved oxygen may be adjusted by appropriately combining these methods. Moreover, you may adjust the amount of dissolved oxygen using a ladle heating type refining apparatus, a simple molten steel processing facility, etc. instead of the RH type degassing refining apparatus. In this case, since the amount of dissolved oxygen cannot be adjusted by vacuum C deoxidation, a method of adding a deacidifying element such as Si may be employed to adjust the amount of dissolved oxygen. When employing a method of adding a deoxidizing element such as Si, the deoxidizing element may be added when steel is removed from the converter to the ladle.

  The form of REM, Ca, Zr, Ti added to the molten steel is not particularly limited. For example, as REM, pure La, pure Ce, pure Y, or pure Ca, pure Zr, pure Ti, and further Fe-Si- REM alloys such as La alloy, Fe-Si-Ce alloy, Ca alloys such as Fe-Si-Ca alloy, Fe-Ca alloy, Ni-Ca alloy, REM-Ca alloys such as Fe-Si-La-Ce alloy, etc. May be added. Moreover, you may add misch metal to molten steel. Misch metal is a mixture of cerium group rare earth elements, and specifically contains about 40 to 50% of Ce and about 20 to 40% of La. However, since misch metal often contains Ca as an impurity, when the misch metal contains Ca, the range specified in the present invention must be satisfied.

The steel material of the present invention has a composite structure composed of a soft phase and a hard phase, and the ratio (Hv ₁ / Hv ₂ ) of the Vickers hardness Hv ₁ of this hard phase to the Vickers hardness Hv ₂ of the soft phase is within a predetermined range. In order to obtain such a structure, for example, the following methods (1) to (3) may be followed. In addition, the temperature shown with the following method is managed by t (plate thickness) / 4 site | part (a management method is mentioned later).

(1) A steel slab having the chemical composition as described above is heated to 950 ° C. or more and 1250 ° C. or less, and rolling is finished in a temperature range from a heating temperature to an Ar ₃ transformation point, and cooling at 20 ° C./second or more. The first accelerated cooling is performed at a speed, and after cooling to 600 to 700 ° C., the temperature is maintained for 10 to 100 seconds (the cooling may be performed at a cooling rate of 0.5 ° C./second or less). Thereafter, the second accelerated cooling is performed at a cooling rate of 5 ° C./second or more to 400 ° C. or less. In this method, cooling is performed after rolling, and the structure is supercooled to increase the nucleation sites, and as the ferrite is refined, the hard phase is finely dispersed, and the composite structure of the hard phase and the soft phase It can be. The reason for setting the range of each condition in this method is as follows.

  When the heating temperature is less than 950 ° C., the rolling temperature becomes too low, and when it exceeds 1250 ° C., the austenite grains become coarse and the base material toughness deteriorates. Therefore, it is necessary to heat at 950 to 1250 ° C.

Rolling temperature: When the rolling temperature is lower than the Ar ₃ transformation point, anisotropy occurs in the structure and the impact absorption energy may be lowered, and the rolling load is increased in production and the productivity is lowered.

  First accelerated cooling rate: By performing accelerated cooling, γ becomes a supercooled state, and transformation is suppressed to a low temperature. Thereafter, the transformation is performed at a low temperature, so that a ferrite having a high transformation driving force and a uniform and fine structure is generated. If the cooling rate is less than 20 ° C./second, partial transformation occurs during accelerated cooling, and uniform refinement of the structure cannot be achieved.

  Cooling stop temperature: When the stop temperature is lower than 600 ° C., the ferrite becomes acicular or a bainite structure. Although the acicular ferrite has good toughness, the hardness is higher than that of the polygonal ferrite, and the hardness difference from the second phase is reduced. Therefore, the effect of suppressing crack propagation at the phase boundary is small. On the other hand, when the cooling stop temperature exceeds 700 ° C., the transformation is slow at a predetermined holding temperature, and a sufficient ferrite fraction (for example, 20 area% or more) cannot be secured, and the crystal grains become coarse and toughness Will deteriorate.

  Holding time after cooling: If this holding time is less than 10 seconds, the transformation is not sufficient, the ferrite fraction is not sufficient, and there is no room for C to concentrate to unreacted γ. Further, when the holding time exceeds 100 seconds, the productivity is lowered, the equilibrium state is approached, and the generation of pearlite can be seen. This pearlite has a layered structure of ferrite and cementite, but cementite is brittle and causes brittle fracture at the crack tip, so that the effect of suppressing crack propagation is small.

  Second accelerated cooling rate: If this cooling rate is less than 5 ° C./second, ferrite + pearlite is generated from untransformed austenite in the cooling stage, and the hardness of the hard phase is not sufficient.

  Final cooling stop temperature: If the stop temperature at this time exceeds 400 ° C., the hard phase is softened by self-tempering and the hardness cannot be sufficiently secured, so the cooling stop temperature needs to be 400 ° C. or less. Yes, preferably 300 ° C. or lower.

(2) a steel slab having a chemical composition as described above, 950 ° C. or higher, then heated to 1250 ° C. or less, and terminates the rolling in a temperature range of the heating temperature to Ar ₃ transformation point, (Ar ₃ transformation point -30 ° C.) or air-cooled to a temperature range of ~ (Ar ₁ transformation point + 30 ° C.), or 5 ° C. / sec after cooling the following cooling rate, to an accelerated cooling at 5 ° C. / sec or more cooling rate. The reason for setting the range of each condition in this method is as follows.

  When the heating temperature is less than 950 ° C., the rolling temperature becomes too low, and when it exceeds 1250 ° C., the austenite grains become coarse and the base material toughness deteriorates. Therefore, it is necessary to heat at 950 to 1250 ° C.

Rolling temperature: When the rolling temperature is lower than the Ar ₃ transformation point, anisotropy occurs in the structure and the impact absorption energy may be lowered, and the rolling load is increased in production and the productivity is lowered.

Cooling rate: Air cooling to a temperature range of (Ar ₃ transformation point−30 ° C.) to (Ar ₁ transformation point + 30 ° C.) or cooling accelerated cooling at a cooling rate of 5 ° C./second or less to By forming a hard phase from untransformed γ in which C is concentrated by subsequent accelerated cooling with ferrite (α) + γ, a composite structure of soft phase + hard phase can be obtained. When the cooling rate is higher than 5 ° C./second and the holding time is not taken, the time for concentrating C to the untransformed γ is small, and a sufficient hard phase is obtained even by the subsequent accelerated cooling. Not only can it not be obtained, but the uniformity in the thickness direction will be reduced.

Cooling stop temperature: When the stop temperature exceeds (Ar ₃ transformation point −30 ° C.), almost no ferrite is formed, and when it is less than (Ar ₁ transformation point + 30 ° C.), almost the transformation is completed to ferrite + pearlite. Therefore, a soft phase + hard phase cannot be obtained.

  Second cooling rate: When the cooling rate is less than 5 ° C./second, ferrite + pearlite is generated from untransformed austenite in the cooling stage, and the hardness of the hard phase is not sufficient.

  Final cooling stop temperature: If the stop temperature at this time exceeds 400 ° C., the hard phase is softened by self-tempering and the hardness cannot be sufficiently secured, so the cooling stop temperature needs to be 400 ° C. or less. Yes, preferably 300 ° C. or lower.

(3) The steel slab having the chemical composition as described above is heated to 950 ° C. or more and 1250 ° C. or less, and rolling is finished in the temperature range from the heating temperature to the Ar ₃ transformation point, and cooling at 10 ° C./second or more. The first accelerated cooling is performed at a rate of 400 ° C. or lower, and then reheating to a temperature range of (Ac ₁ transformation point + 30 ° C.) to (Ac ₃ transformation point−30 ° C.), followed by a cooling rate of 5 ° C./second or more. Then, the second accelerated cooling is performed. In this method, the structure unit can be made fine by making the structure before reheating a quenching structure, and by reheating above the Ac ₁ transformation point, high temperature tempered bainite or martensite + austenite structure Become. Carbide diffuses from tempered bainite and martensite to reverse-transformed austenite, and the hardness of tempered bainite and martensite is greatly reduced, and then γ enriched with C is transformed into a hard phase by accelerated cooling. It can be a complex structure of phases. The reason for setting the range of each condition in this method is as follows.

  When the heating temperature is less than 950 ° C., the rolling temperature becomes too low, and when it exceeds 1250 ° C., the austenite grains become coarse and the base material toughness deteriorates. Therefore, it is necessary to heat at 950 to 1250 ° C.

Rolling temperature: When the rolling temperature is lower than the Ar ₃ transformation point, anisotropy occurs in the structure and the impact absorption energy may be lowered, and the rolling load is increased in production and the productivity is lowered.

  Cooling rate, cooling stop temperature: When the cooling rate is less than 10 ° C / second or the cooling stop temperature exceeds 400 ° C, the structure does not become a tempered structure, so the grain size becomes coarse, and fatigue crack growth resistance along with toughness Sex is reduced.

If the reheating temperature is less than (Ac ₁ transformation point + 30 ° C.), the α → γ transformation hardly occurs and a sufficient hard phase cannot be secured. When (Ac ₃ transformation point + 30 ° C.) is exceeded, most of them undergo α → γ transformation after reheating, and all of them become a hard phase by subsequent quenching.

  Second accelerated cooling rate: When the cooling rate is less than 5 ° C./second, the hardness of the hard phase is not sufficient.

  Final cooling stop temperature: If the stop temperature at this time exceeds 400 ° C., the hard phase is softened by self-tempering and the hardness cannot be sufficiently secured, so the cooling stop temperature needs to be 400 ° C. or less. Yes, preferably 300 ° C. or lower.

  The steel material of the present invention thus obtained can be used, for example, as a material for structures such as bridges, high-rise buildings, ships, etc., and toughness degradation of the weld heat-affected zone not only in small to medium heat input welding but also in large heat input welding. While being able to prevent, it is possible to ensure excellent fatigue crack growth resistance.

  Hereinafter, the present invention will be described in more detail with reference to examples. However, the following examples are not intended to limit the present invention, and may be implemented with appropriate modifications within a range that can meet the purpose described above and below. These are all possible and are within the scope of the present invention.

  After the hot metal was first refined in a 240-ton converter, the steel was removed from the converter into a ladle and subjected to secondary refining while adjusting the components and adjusting the temperature. Here, in the ladle, the amount of dissolved oxygen shown in Table 1 below was adjusted by the deoxidation method shown in Table 1 below. Thereafter, the elements were added in the order shown in Table 1 below. Subsequently, the remaining alloying elements were added as necessary to finally adjust the compositions shown in Table 2 below. In the secondary refining, dehydrogenation and desulfurization were performed using an RH type degassing refining apparatus. Further, in Table 1, the chemical component No. A dissolved oxygen amount “−” of 16 indicates that it is less than the limit of quantification.

  In Table 1, La is in the form of an Fe-La alloy, Ce is in the form of an Fe-Ce alloy, REM is in the form of a misch metal containing about 50% La and about 25% Ce, and Ca is Ni. Zr was added in the form of Zr alone, and Ti was added in the form of an Fe-Ti alloy in the form of -Ca alloy, Ca-Si alloy, or Fe-Ca compact.

  In Table 2, “-” indicates that no element was added, and “less than” means that no element was added, but it was inevitably contained, so that it was detected within the range below the limit of quantification. is doing.

The molten steel after component adjustment was cast into a slab with a continuous casting machine, and then hot-rolled to produce various steel plates. The transformation points (Ar ₃ , Ar ₁ , Ac ₁ , Ac ₃ ) shown in Table 2 are values obtained by the following formulas (1) to (4). The production conditions at this time are shown in Tables 3 and 4 below. The temperature at this time is managed by the temperature at the position of t / 4 (t is the plate thickness), and the detailed temperature management procedure is as follows.
Ar ₃ = 868−369 · [C] + 24.6 · [Si] −68.1 · [Mn] −36.1
[Ni] -20.7, [Cu] -24.8, [Cr] +29.6, [Mo] +
190 ・ [V] (1)
Ar ₁ = 630.5 + 51.6 · [C] + 12.4 · [Si] −64.8 · [Mn]
-57.5 · [Mo] (2)
Ac ₁ = 723-14. [Mn] +22. [Si] -14.4. [Ni] +23.3.
[Cr] (3)
_{Ac 3 = 908-223.7 · [C]} +30.49 · [Si] -34.3 · [Mn]
+ 37.92 · [V] -23.5 · [Ni] (4)
However, [C], [Si], [Mn], [Ni], [Cu], [Cr], [Mo] and [V] are respectively C, Si, Mn, Ni, Cu, Mo and V. Content (mass%) is shown.

[Temperature management procedure]
1. Using a process computer, the heating temperature at an arbitrary position (for example, t / 4 position) from the front surface to the back surface of the steel slab is calculated based on the atmospheric temperature from the start of heating to the end of heating and the in-furnace time.
2. Using the calculated heating temperature, based on the rolling pass schedule during rolling and the data of the cooling method (water cooling or air cooling) between passes, a method suitable for calculation such as the difference method is used to calculate the rolling temperature at any position in the plate thickness direction. The rolling is carried out while using the calculation.
3. The surface temperature of the steel sheet is measured using a radiation type thermometer installed on the rolling line. However, the theoretical value is also calculated in the process computer.
4). The surface temperature of the steel sheet measured at the start of rough rolling, at the end of rough rolling, and at the start of finish rolling is collated with a calculated temperature calculated from a process computer.
5). If the difference between the calculated temperature and the measured temperature is ± 30 ° C or more, recalculate the calculated surface temperature so that it matches the measured temperature to obtain the calculated temperature on the process computer. The calculated temperature is used as it is.
6). Using the calculated temperature calculated above, the rolling temperature in the region to be controlled is managed.

For each steel plate obtained as described above, fatigue crack growth rate, (hard phase / soft phase) hardness ratio (Hv ₁ / Hv ₂ ), soft phase particle size, and investigation of inclusion composition by EPMA And HAZ toughness were evaluated in the following manner.

[Fatigue crack growth rate]
The hot-rolled material was cut, and the fatigue crack growth rate was determined by conducting a fatigue crack growth test using a compact test piece in accordance with ASTM E647. At this time, the value in the stable growth region ΔK = 20 (MPa · √m) where the Paris law defined by the following equation (5) is satisfied was evaluated as a representative value. Regarding the evaluation and standard of the fatigue crack growth rate, the normal steel material has a growth rate of about 4.0 to 6.0 × 10 ⁻⁵ mm / cycle (when ΔK = 20). The standard was × 10 ⁻⁵ mm / cycle or less.
da / dn = C (ΔK) ^m (5)
Here, a: crack length, n: number of repetitions, C, m: constants determined by matters such as material and load, respectively.

[Hardness ratio of (hard phase / soft phase)]
The Vickers hardness Hv _{1 of the} hard phase and the Vickers hardness Hv _{2 of the} soft phase were measured using a 10 gf micro Vickers hardness meter, and the average value of each of the five points was determined, and the hardness ratio (Hv ₁ / Hv ₂ ) Was calculated.

[Measurement method of particle size of soft phase]
(A) It cut | disconnected in the direction parallel to the rolling direction of steel materials, and the sample containing the front and back surface part of board thickness was prepared.
(B) Polishing was performed using a wet emery polishing paper of # 150 to # 1000 or a polishing method having the same function, and a mirror finish was performed using an abrasive such as diamond slurry.
(C) The polished sample was corroded using a 3% nital solution (corrosive solution) to reveal the crystal grain boundaries of the soft phase.
(D) The exposed tissue was photographed at a magnification of 100 times or 400 times (taken as a photograph of 6 cm × 8 cm) and taken into an image analyzer (600 μm × 800 μm at 100 times, 150 μm × 200 μm at 400 times) Equivalent). In this capture, the number of sheets corresponding to 1 mm × 1 mm (at least 6 fields of view at 100 × and 35 fields of view at 400 ×) was captured at any magnification.
(E) In the image analysis apparatus, the image was converted into a circle having an area equivalent to that of a region surrounded by one grain boundary, and the diameter of the converted circle was defined as the particle diameter of the equivalent-circle soft phase.
(F) The average of the values measured for all visual fields was calculated as the average equivalent-circle soft phase particle size.

[Investigation of inclusion composition]
A sample was cut out from the cross section at the t (plate thickness) / 4 position of each steel plate. The cut sample surface was observed 600 times using “EPMA-8705 (device name)” manufactured by Shimadzu Corporation, and the component composition of the precipitate having a maximum diameter of 0.2 μm or more was quantitatively analyzed. The observation conditions are an acceleration voltage of 20 kV, a sample current of 0.01 μA, an observation visual field area of 1 to 5 cm ² , and an analysis number of 100, and the component composition at the center of the precipitate is determined by wavelength dispersion spectroscopy of characteristic X-rays. analyzed. The analysis target elements are Al, Mn, Si, Ti, Zr, Ca, La, Ce, and O, and a relationship between the electron beam intensity and the element concentration of each element is obtained in advance using a known substance as a calibration curve. The element concentration of the precipitate was determined from the electron beam intensity obtained from the precipitate and the calibration curve.

Of the obtained quantitative results, a precipitate having an oxygen content of 5% or more was defined as an oxide, and the average was defined as the average composition of the oxide. Note that the oxide of the oxide and REM of Ti, expressed a metal element in M, is present in the form of M ₂ O ₃ and M ₃ O _5, MO ₂ in the steel material, these oxides M ₂ The oxide composition was calculated in terms of O ₃ . When a plurality of elements were observed from one inclusion, the composition of the oxide was calculated in terms of a single oxide of each element from the ratio of X-ray intensity indicating the presence of these elements. The “others” in the following 5 and 6 is the total amount of oxides of elements not analyzed (for example, MgO).

As a result of observing the surface of the sample with EPMA, most of the observed oxide was a composite oxide containing REM and / or Ca and Zr, or a composite oxide further containing Ti. As a result, oxides of REM, CaO, ZrO ₂ and Ti ₂ O ₃ were also generated.

[Evaluation of HAZ toughness]
The welding reproduction test shown below was performed simulating large heat input welding. This welding reproduction test was performed by heating the whole test piece (125 mm × 32 mm × 55 mm test piece) cut out from the slab to 1400 ° C., holding at this temperature for 30 seconds or 50 seconds, and then cooling. . The cooling rate at this time was adjusted so that the cooling time at 800 to 500 ° C. was 400 seconds. The conditions of this reproduction test cycle correspond to forming a bond portion when welding is performed by electroslag welding (ESW) or submerged arc welding (SAW) with a heat input of 40 to 60 kJ / mm. About each test piece which performed the said reproduction | regeneration heat cycle, the V notch Charpy test (JISZ2202) was done and the absorbed energy (vE- ₄₀ ) in _-40 degreeC was calculated | required. And it evaluated that the value of vE- ₄₀ was 100J or more that it was excellent in HAZ toughness.

  The investigation results of the average composition of all oxides are shown in Tables 5 and 6 below. The measurement results of the fatigue test progress rate, the hardness ratio, and the soft phase particle diameter (equivalent circle diameter) are collectively shown in Table 7 below together with the HAZ toughness. , 8.

These results can be considered as follows. First, it can be seen that the REM oxide and / or the one not containing CaO and ZrO ₂ (steel plates No. 32-41) is inferior in HAZ toughness.

On the other hand, with respect to the fatigue crack growth rate, those out of the preferable manufacturing conditions (steel plates No. 2, 3, 6, 7, 9, 10, 12, 13, 15, 16, 20, 21, 21, 24, 20 and In 30), since the crystal grains become coarse or sufficient hard phase hardness cannot be obtained, the hardness ratio (Hv ₁ / Hv ₂ ) does not become an appropriate value, and the fatigue crack growth rate increases. I understand that Based on this data, the relationship between the hardness ratio (Hv ₁ / Hv ₂ ) and the fatigue crack growth rate is shown in FIG. 1. By defining the hardness ratio in the range of 1.5 to 5.0, fatigue It can be seen that the crack growth rate is low.

It is a graph which shows the relationship between hardness ratio and fatigue crack growth rate.

Claims (9)

C: 0.03 to 0.18% (meaning “mass%”; the same shall apply hereinafter)
Si: 0.5% or less (excluding 0%),
Mn: 0.9-2.0%, and N: 0.003-0.01%,
P: 0.02% or less (excluding 0%),
S: 0.015% or less (not including 0%) and Al: 0.01% or less (not including 0%),
REM: 0.001-0.1% and / or Ca: 0.0003-0.02%,
Zr: 0.001 to 0.05% each contained,
The balance is steel consisting of iron and inevitable impurities,
REM and / or Ca and Zr as a single oxide or composite oxide, and a composite structure composed of a soft phase and a hard phase, and Vickers hardness Hv _{1 of the} hard phase and Vickers hardness of the soft phase a is the ratio of _{Hv 2 (Hv 1 / Hv 2} ) is 1.5 to 5.0, the toughness of the weld heat affected zone characterized and in that the particle size of the soft phase is 20μm or less in circle equivalent diameter of fatigue Steel material with excellent resistance to crack growth. And measuring the composition of the total oxides contained in the steel material, when mass conversion as a single oxide, the total of the oxides and / or CaO of R EM least 5%, and the ZrO ₂ is more than 5% The steel material according to claim 1, wherein:
  The steel material further contains Ti: 0.08% or less (not including 0%) as another element and contains the Ti as a single oxide or a composite oxide. Steel materials described.   The steel material according to claim 3, wherein when the composition of all oxides contained in the steel material is measured and converted into mass as a single oxide, the Ti oxide satisfies 0.3% or more. The steel material is still another element,
Cu: 2% or less (excluding 0%),
Ni: 3.5% or less (excluding 0%),
Cr: 3% or less (excluding 0%),
Mo: 1% or less (excluding 0%),
Nb: 0.25% or less (excluding 0%),
V: 0.1% or less (not including 0%), and B: 0.005% or less (not including 0%)
The steel material according to any one of claims 1 to 4, comprising at least one element selected from the group consisting of:   The soft phase is at least one selected from the group consisting of ferrite, tempered bainite and tempered martensite, and the hard phase is bainite and / or martensite (including island martensite). A steel material according to any one of the above. A method for producing the steel material according to any one of claims 1 to 6,
To the molten steel with the dissolved oxygen content adjusted to the range of 0.0020-0.010%,
A method for producing a steel material excellent in toughness and fatigue crack growth resistance of a weld heat affected zone, characterized by adding at least one element selected from the group consisting of REM and Ca and Zr. A method for producing the steel material according to any one of claims 3 to 6,
To the molten steel with the dissolved oxygen content adjusted to the range of 0.0020-0.010%,
A method for producing a steel material excellent in toughness and fatigue crack growth resistance of a weld heat affected zone, comprising adding at least one element selected from the group consisting of REM and Ca, and Ti and Zr.   The method according to claim 8, wherein Ti is added to the molten steel with the dissolved oxygen content adjusted before adding at least one element selected from the group consisting of REM and Ca and Zr.

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