Method of manufacturing thick steel product of high strength and high toughness having excellent weldability and minimal variation of structure and physical properties

Information

  • Patent Grant
  • 5989366
  • Patent Number
    5,989,366
  • Date Filed
    Friday, March 14, 1997
    27 years ago
  • Date Issued
    Tuesday, November 23, 1999
    24 years ago
Abstract
A method of manufacturing a thick steel product of high strength and high toughness having excellent weldability with minimal variation of material properties, comprises heating a steel raw material to the temperature of Ac.sub.3 to 1350.degree. C., hot rolling and then cooling at the cooling rate of 10.degree. C./sec. or less. The steel raw material has the following composition:C: 0.001-0.25 wt %;Mn: 1.0-3.0 wt %;Ti: 0.005-0.20 wt %;Nb: 0.005-0.20 wt %;B: 0.0003-0.0050 wt %; andAl: 0.01-0.100 wt %balance substantially Fe and incidental impurities. The composition has a transformation start temperature (Bs) of 670.degree. C. or less. Since the steel product obtained by the method has no variation in physical properties regardless of variation in cooling rate, it is possible to supply steel products of high strength and high toughness which have uniform microstructure and properties along their thickness direction and are excellent in weldability.
Description

BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates to a method of manufacturing a steel product such as a thick steel plate, steel strip, shape steel, steel bar and the like io used in the fields of construction, ocean structures, pipes, ship building, reservoirs, civil engineering, construction machinery and the like, and, in particular, a thick steel product of high strength and high toughness having excellent weldability and minimal variation of structure and physical properties.
2. Description of the Related Art
A thick steel product such as thick steel plate has been used in various fields as described above and the characteristics thereof such as increased strength and toughness have been improved. In particular, recently, it is required that these characteristics are uniform in a thickness direction of the product, and less variable among a plurality of steel products.
One reason for that requirement is illustrated by the fact that, as buildings are made increasingly tall, they are designed so that vibration energy resulting from a large earthquake is absorbed by the controlled deformation of a building to prevent its chaotic collapse, as described in "Iron and Steel, 1988, No. 6" ("Testu to Hagane Dai 74 Nen (1988), Dai 6 Gou"), page 11-page 21. More specifically, when an earthquake occurs, the framework of the building is partially collapsed in a predetermined shape so that the total or chaotic collapse of the building is prevented by the plasticization of the framework. However, since this idea is based on the premise that when an earthquake occurs, the framework of a building exhibits a behavior intended by a designer, the designer must know precisely the yield strength ratio of the steel products used for the columns, beams and the like of the building. Therefore, it is indispensable that steel products such as steel plates, H-sections and the like used for the columns, beams and the like are uniform, and variation in the strength of the steel products is a serious problem.
Since it is necessary that steel products used for building and ship building have high tensile strength and high toughness, it is conventional to manufacture this type of steel product by a thermo-mechanical control process (hereinafter referred to as TMCP method). However, when thick steel products are made by the TMCP method, the structure of them is varied because the cooling rate in a cooling process executed after rolling is different along the thickness direction of a given product, or among several such products. This problem occurs because the cooling rate is large in the vicinity of the surface of the steel products when they are cooled, whereas the cooling rate is small at the center of the steel products, in thickness direction thereof. As a result, the material of the thus obtained steel products varies along the thickness direction of a given piece, and/or among a plurality of pieces. The variation of the material appears between the webs and between the flanges of an H-section due to the irregular cooling therebetween or among respective lots; additionally, it appears as a particular problem along the thickness direction of a thick steel plate.
To cope with the above problem, Japanese Unexamined Patent Publication No. 63-179020 discloses a method of reducing the difference of hardness of the cross section of a steel plate in a thickness direction by controlling components, a rolling reduction ratio, a cooling rate and a cooling finishing temperature. However, when a thick steel plate, in particular, a very thick steel plate having a thickness exceeding 50 mm is made, since a cooling rate inevitably varies along the thickness direction thereof, it is difficult to suppress the difference of hardness of the cross section in the plate thickness direction.
Japanese Unexamined Patent Publication No. 61-67717 discloses a method of greatly reducing the difference of strength in a plate thickness direction by greatly reducing a C content. As shown in FIG. 3 of the publication, however, the method cannot correct the variation of strength caused by the change of a cooling rate which inevitably arises particularly in a thick steel plate.
Japanese Unexamined Patent Publication No. 58-77528 describes that stable distribution of hardness is obtained by the complex addition of Nb and B. However, since the cooling rate must be controlled to the range of 15-40.degree. C./sec to form bainite, and it is difficult to strictly control the cooling rate at the center of a plate in the thickness direction thereof, there is a problem that a uniform microstructure cannot be obtained in the thickness direction of the plate, strength is variable, and ductility and toughness are deteriorated due to the formation of island-shaped martensite.
Furthermore, it is important that the steel product used for the above applications have high toughness and a tensile strength greater than 570 MPa. For this purpose, a method of obtaining a fine tempered martensitic structure by a process of reheating, quenching and tempering has been mainly used. However, this method has a problem in that high cost is associated with the reheating, quenching and tempering process and further since a weld cracking parameter (hereinafter referred to as P.sub.cm), which is the index of weldability, increases due to an increased quenching property, and weldability is thereby deteriorated.
On the other hand, Japanese Unexamined Patent Publication No. 62-158817 discloses a method of obtaining a thick steel plate having high strength at a relatively low P.sub.cm by executing a tempering process after rapid cooling while using the precipitation of Nb and Ti. In this method, however, there is a fear that distortion is caused by irregular cooling in addition to the high cost of a quenching and tempering process.
Likewise, although Japanese Unexamined Patent Publication No. 55-100960 discloses steel whose weldability is enhanced by regulating P.sub.cm and limiting the amounts of C, N and S, it is difficult to prevent the significant variation in strength along the thickness direction thereof.
Further, Japanese Unexamined Patent Publication No. 54-132421 discloses making high tension bainite steel by hot rolling executing at a finishing temperature of 800.degree. C. or less to obtain toughness, and greatly reducing a C content to use the steel as pipeline raw material. However, this method has a problem that since the hot rolling is finished in a low temperature region, when a plate must be slit lengthwise, not only distortion and warping are liable to be caused by the slitting but also variation arises between the strength in a rolling direction (L direction) and the strength in the direction perpendicular to the L direction (C direction) by the rolling executed in the low temperature region.
An object of the present invention is to provide a method of manufacturing a steel product free from the above problems, that is, a steel product which is not restricted by the cooling rate after rolling, has minimal variation of microstructure along its thickness direction and among plural products, is excellent in weldability and has high toughness of 570 MPa or more in terms of tensile strength.
SUMMARY OF THE INVENTION
The variation of material properties of a thick steel plate is caused by the change in microstructure resulting from the great change of the cooling rate during a cooling process, along the thickness direction of the steel plate from the surface to the center thereof, or from the change of the cooling rate during the cooling process due to the variation of manufacturing conditions. It is important to obtain a homogenous microstructure despite operating over a wide range of cooling rate, to avoid variation of the material properties.
The inventors have found that careful selection of the constituent components of the steel composition permits the manufacture of a steel plate which has minimal variation of material properties and whose microstructure in a thickness direction is unchanged regardless of the change of a cooling rate, as a result of developing a method for obtaining a homogeneous microstructure even if the manufacturing conditions are changed. In particular, a bainite single phase structure can be made by the addition of Nb and B with ultra low C and a large amount of Mn, whose formation is independent of cooling rate.
According to the present invention, since the steel used in the present method contains ultra low C, martensite is not created even at a large cooling rate; moreover, since ferrite is not created due to the addition of high Mn, Nb and B even at a small cooling rate, a bainite single phase can be achieved over a wide range of cooling rate. As a result, the microstructure and strength of the steel are difficult to be affected by the cooling rate and the difference of strength among respective steel products is reduced.
The inventors have also found that since P.sub.cm is made small by sharply reducing the C content, not only excellent weldability is obtained but also sufficient strength is achieved by the bainite single phase and that sufficient toughness is obtained by achieving a granular bainite ferrite structure by formulating the composition such that a microstructure is formed even under a small rolling reduction as compared with a conventional low carbon bainite structure. The inventors have solved the above problems by comprehensively combining the above discoveries.
That is, the present invention is a method of manufacturing a thick steel product of high strength and high toughness having excellent weldability and minimal variation in structure and material properties, comprising the steps of heating a steel raw material to a temperature in the range from AC.sub.3 to 1350.degree. C., hot rolling and then cooling the steel raw material at a cooling rate of 10.degree. C./sec or less. The steel raw material used in the present method comprises a composition containing the following components:
C: 0.001-0.025 wt %;
Mn: 1.0-3.0 wt %;
Ti: 0.005-0.20 wt %;
Nb: 0.005-0.20 wt %;
B: 0.0003-0.0050 wt %; and
Al: 0.01-0.100 wt %
balance substantially Fe and incidental impurities, the composition having a transformation start temperature (Bs) of 670.degree. C. or less.
Other aspects of the present invention will be apparent from the following detailed description.





BRIEF DESCRIPTION OF THE DRAWINGS
FIG. 1 is a photograph of the microscopic structure of a fine granular bainite ferrite structure; and
FIG. 2 is a graph showing the relationship between cooling rate and strength in a thick steel plate.





DETAILED DESCRIPTION OF PREFERRED EMBODIMENTS
Initially, it will be described why the weight percent ranges of the respective chemical components of the steel product of the present invention are established in the manner disclosed.
C: 0.001-0.025 wt %
Although it is necessary to provide C in 0.001 wt % or more, when its content exceeds 0.025 wt % toughness is greatly decreased at a welded portion and it is difficult to make a microstructure to a granular bainite ferrite structure, so the C content is chosen to be 0.001-0.025 wt %.
Mn: 1.0-3.0 wt %
Mn should be contained in 1.0 wt % or more in order to lower the transformation start temperature, thereby to obtain a fine granular bainite ferrite structure. However, since toughness is deteriorated by a content exceeding 3.0 wt %, the range of from 1.0-3.0 wt % is chosen.
Ti: 0.005-0.20 wt %
Ti should be present in an amount of 0.005 wt % or more to enhance the toughness in a heat affected zone (HAZ); however, its effect is saturated when the content exceeds 0.20 wt %, and so the upper endpoint of the range is set to 0.20 wt % simply from the view point of cost reduction.
Nb: 0.005-0.20 wt %
Nb should be present in an amount of 0.005 wt % or more to lower the transformation start temperature, thereby to obtain a fine granular bainite ferrite structure; however, its effect is likewise saturated when the content exceeds 0.20 wt %, and so the upper endpoint of the range is set to 0.20 wt % also for the sake of cost reduction.
B: 0.0003-0.0050 wt %
Addition of B in a slight amount is effective to restrict the creation of ferrite nuclei by reducing the grain boundary energy of the former .gamma. grain boundary, and so it should be present in an amount of 0.0003 wt % or more to obtain a fine granular bainite ferrite structure. On the other hand, when the content of B exceeds 0.0050 wt %, toughness is deteriorated by formation of B compounds such as BN and the like, and so the range is set to 0.0003-0.0050 wt %.
Al: 0.01-0.100 wt %
Al is necessary in 0.01 wt % or more as a deoxidizing agent. However, since the cleanness of steel is deteriorated when its content exceeds 0.100 wt %, it should be present in an amount of 0.100 wt % or less.
Furthermore, it is important that the above components have a transformation start temperature (B.sub.s) of 670.degree. C. or less.
That is, as a result of the diligent experimentation by the inventors as to the relationship between the toughness and the microstructure of ultra low carbon steel, the inventors have discovered that a fine granular bainite structure as shown more particularly in FIG. 1 has the greatest toughness among the microstructures of ultra low carbon steel. The control of the microstructure permitted the deterioration of toughness to be greatly reduced as compared with conventional steel, even if a rolling finish temperature was increased. When a method of obtaining this microstructure was examined, it was found that there was a good relationship between a microstructure and a transformation start temperature. This is because when steel products were obtained by changing rolling conditions from steels having various components in the range of C: 0.002-0.020 wt %, Mn: 1.2-2.0 wt %, Ni: 0.0-2.0 wt %, Ti: 0.01 wt %, Nb: 0.005-0.08 wt %, B: 0.0010-0.0018 wt %, Cu: 0.0-1.22 wt % and Al: 0.01-0.100 wt % and the relationship between the transformation start temperature B.sub.s and the microstructure of the steel products was investigated while they were cooled after rolling, it was found that a fine granular bainite ferrite structure could be obtained when B.sub.s was set to 670.degree. C. or less.
Still further, it is preferable that the composition of the above components satisfies the following formula (1) or (2).
130 Mn+2500 Nb.gtoreq.296 (1)
130 Mn-13Ni+2500 Nb+55 Cu.gtoreq.296 (2)
Since the transformation start temperature B.sub.s was affected by the composition of the components, when multiple regression analysis was carried out as to the amounts of Mn, Ni, Nb and Cu which particularly greatly changed B.sub.s, the relationship of B.sub.s =966-130 Mn+13 Ni-2500 Nb-55 Cu could be obtained. On the other hand, since the granular bainite structure can be obtained by setting the transformation start temperature B.sub.s to 670.degree. C. or less, it is important that the following formula be satisfied.
966-130 Mn+13 Ni-2500 Nb-55 Cu.ltoreq.670
The rearrangement of the above formula results in the following formula.
130 Mn-13 Ni+2500 Nb+55 Cu.gtoreq.296 (2)
When the composition of the components of the above formula (2) does not contain Ni and Cu, the following formula (1) can be obtained.
130 Mn+2500 Nb.gtoreq.296 (1)
Note, when the transformation start temperature B.sub.s exceeds 670.degree. C., the fine granular bainite structure cannot be obtained as well as when the cooling rate after the rolling is reduced, strength is made insufficient by the precipitation of ferrite.
The present invention is further characterized in that a homogenous microstructure, more specifically, a microstructure at least 90% of which is composed of a granular bainite ferrite structure, can be obtained by adjusting the components to provide the above basic composition, virtually independent of the cooling rate after rolling. This feature will be apparent from the experiment whose results are shown in FIG. 2.
That is, FIG. 2 shows the result of investigation of the tensile strength of steel plates which were obtained by variously changing a cooling rate between 0.1.degree. C./sec. and 50.degree. C./sec. in the manufacturing process of steel whose components were adjusted according to the present invention (example of the present invention) and conventional steel (conventional example) used as building material. It is found from FIG. 2 that a definite strength can be obtained by the adjustment of the components according to the present invention without depending upon the cooling rate. In particular, the variation of the values of YS and TS is reduced over a wide range of the cooling rate, which could not be conventionally anticipated. This results from the addition of Mn, Ti and B in suitable amounts. Therefore, even if the cooling rate differs along the thickness direction of a thick steel plate, the strength is not correspondingly changed depending upon the cooling rate, and a thick steel plate whose microstructure and physical properties are more uniform along a thickness direction can be obtained.
Note, the example of the present invention contained C: 0.013 wt %, Mn: 1.60 wt %, Ti: 0.01 wt %, Nb: 0.065 wt %, B: 0.0015 wt % and Al: 0.035 wt % and the balance was Fe and incidental impurities. On the other hand, the conventional example contained C: 0.14 wt %, Si: 0.4 wt %, Mn: 1.31 wt %, Al: 0.024 wt %, Nb: 0.015 wt % and Ti: 0.013 wt %. Then, a series of thick steel plates having a thickness of 50 mm were made by changing the cooling rate in the same manufacturing process and there was measured the tensile strength of the test pieces obtained from the respective thick steel plates.
The simultaneous addition of V: 0.04-0.15 wt % and N: 0.0035-0.0100 wt % in addition to the above basic components can result in faster formation of fine bainite. That is, when V is used together with N, it has an action for creating a VN precipitate and increasing bainite transformed nuclei. For this purpose, V and N should be contained in at least 0.04 wt % and 0.0035 wt %, respectively. On the other hand, when V and N exceed 0.15 wt % and 0.0100 wt %, respectively, no improved is obtained in the more rapid formation of fine bainite, and, further, the toughness of a welded metal and at HAZ is deteriorated. Therefore, they are present in the ranges of V: 0.04-0.15 wt % and N: 0.0035-0.0100 wt %.
Additionally, the present invention can optionally control the level of strength and toughness by the addition of predetermined chemical components to the above basic components. At the time, since the homogeneous microstructure which has been achieved is not affected by the addition of the new components, a thick steel plate of high strength and/or high toughness with minimal variation of properties can be easily obtained.
First, at least one component selected from Si: 0.60 wt % or less, Cr: 0.2 wt % or less, Ni: 0.05-2.0 wt %, Mo: 0.5 wt % or less, W: 0.5 wt % or less, V: 0.005-0.04 wt % and Cu: 0.05-0.7 wt % can be added to enhance strength. Since these components are effective even if they are added in a slight amount, the lower limit of addition can be set as desired, with the exception of V. Note, when V is added in the range of from 0.04-0.15 wt % to make bainite fine as described above, an action similar to that shown below can be also expected.
Si: 0.60 wt % or less
Since weldability is impaired by a Si content exceeding 0.60 wt %, it is set to the range of 0.60 wt % or less.
Cr: 0.2 wt % or less
Although Cr is effective to increase the strength of a base metal and a welded portion, weldability and the toughness of HAZ are deteriorated by its presence in excess of 0.2 wt %, and so it is added in the range of 0.2 wt % or less. Note, it is preferable to add Cr in an amount of at least 0.05 wt % to achieve a sufficient strength increasing effect.
Ni: 0.05-2.0 wt %
Although Ni in an amount of 0.05 wt % or more enhances strength and toughness and also prevents cracks in rolling caused by the addition of Cu, since it is expensive and the excessive addition does not improve its effect, it is added in the range of 2.0 wt % or less.
Mo: 0.5 wt % or less
Although Mo is effective to increase strength at ordinary temperature and high temperature, since the addition of it exceeding 0.5 wt % deteriorates weldability, it is added in the range of 0.5 wt % or less. It is preferable to set the lower limit of addition to 0.05 wt %.
W: 0.5 wt % or less
Although W is effective to increase strength at high temperature, since it is expensive and the addition of it exceeding 0.5 wt % deteriorates toughness, it is added in the range of 0.5 wt % or less. Note, it is preferable to set the lower limit of addition to 0.05 wt %.
Cu: 0.05-0.7 wt %
Since Cu is effective to strengthen the precipitation and solid-solution of steel and lower the transformation start temperature B.sub.s, it should be contained in 0.05 wt % or more. On the other hand, since the addition of it exceeding 0.7 wt % increases cost, it is added in an amount of 0.7 wt % or less.
V: 0.005-0.04 wt %
Although V is added in 0.005 wt % or more to strengthen precipitation and further to subject the former .gamma. grains pinning as VN or VC, since the addition of it exceeding 0.04 wt % saturates its effect, the upper limit of addition is set to 0.04 wt %.
Further, at least one component selected from Ca and a rare earth metal (REM) may be added to enhance the toughness of HAZ.
Ca: 0.006 wt % or less
Although Ca is effective to enhance the toughness of HAZ by controlling sulfide inclusions, since the addition of it exceeding 0.006 wt % deteriorates the property of steel by forming coarse inclusions in the steel, it is added in 0.006 wt % or less.
REM: 0.02 wt % or less
Although REM enhances the toughness of HAZ by restricting as oxysulfide the growth of austenite grains, since the addition of it exceeding 0.02 wt % injures the cleanness of steel, it is added in 0.02 wt % or less.
Note, since the addition of Ca and/or REM below 0.001 wt % is insufficient to enhance the toughness of HAZ as described above, it is preferably added in 0.001 wt % or more.
Since the steel having the above components can achieve a homogenous granular bainite ferrite structure by controlling the components of it to the above basic composition, it is not necessary to strictly control manufacturing conditions. Thus, although it suffices only to make the steel plate according to the practice used in the manufacture of this type of the steel, the following manufacturing process can be advantageously employed to secure high strength and weldability together with the limited variation of the material and increased toughness.
That is, it is especially effective for increasing strength and enhancing weldability, to perform a process involving heating a steel slab whose components are adjusted as described above to a temperature within the range from the AC.sub.3 point to 1350.degree. C., and then cooling it at a rate of 10.degree. C./sec. or less; or a process for heating the steel slab to the temperature of Ac.sub.3 point--1350.degree. C., and finishing the hot rolling of it at the final finishing temperature of 800.degree. C. or more and then cooling it at the rate of 10.degree. C./sec. or less.
A reason why the heating temperature is set to the Ac.sub.3 point or higher is to render the microstructure homogeneous by initially making it austenitic; whereas the temperature is set to 1350.degree. C. or less because the surface of a steel product is violently oxidized when the heating temperature exceeds 1350.degree. C.
A reason why cooling rate is executed at 10.degree. C./sec. or less is that when it exceeds 10.degree. C./sec., it is more difficult to obtain a fine granular bainite ferrite structure, and toughness is deteriorated.
When hot rolling is executed, it is advantageous to set the final finishing temperature to 800.degree. C. or more. That is, there is conventionally a problem that when the finishing temperature is lowered to secure toughness in Si--Mn steel, there is caused a difference (hereinafter denoted as difference of strength in L-C) between the strength in a rolling direction (L-direction) and the strength in the direction perpendicular to the L-direction (C-direction). To reduce the difference of strength in L-C, it is effective to increase the finishing temperature or reduce the rolling reduction ratio. When the finishing temperature is increased or the rolling reduction ratio is reduced as described above however, there arises a problem that a microstructure is not made fine and toughness is deteriorated.
On the other hand, since the composition of the components according to the present invention permits the fine granular bainite ferrite structure which is advantageous to toughness to be obtained without the execution of rolling, toughness is not deteriorated even if the finishing temperature is increased and the rolling reduction ratio is reduced and further a homogeneous and fine microstructure can be obtained without the execution of refining. Therefore, since the present invention does not suffer the conventional adverse affect, the difference of strength in L-C can be reduced by increasing the finishing temperature without sacrificing toughness.
Slabs of 100 mm thick were obtained by forging three types of steels, that is, a steel of the present invention (A) containing C: 0.013 wt %, Mn: 1.60 wt %, Ni: 0.3 wt %, Nb: 0.045 wt %, B: 0.0015 wt % and Cu: 0.5 wt %, a conventional steel (B) containing C: 0.15 wt %, Si: 0.3 wt %, Mn: 1.4 wt %, V: 0.05 wt % and Nb: 0.015 and a comparative steel (C) containing C: 0.022 wt %, Si: 0.30 wt %, Mn: 1.75 wt %, Nb: 0.043 wt %, Ti: 0.0015 wt % and B: 0.0012 wt %. These slabs were made into steel plates of 70 mm thickness in such a manner that they are heated at 1150.degree. C. for one hour, rolled by reduction ratio 30% at various finishing temperatures and then cooled by air. Then, various mechanical properties were investigated in test pieces which were collected from the thus obtained steel plates at the portions of 1/2 and 1/4 in their thickness direction. Table 1 shows the result of this investigation. As is apparent from Table 1, the toughness of the steel of the present invention is not deteriorated even if the finishing temperature is set to 800.degree. C. or more at which the difference of strength in L-C is lowered.
TABLE 1__________________________________________________________________________ T.S in L T.S in C Difference of Finished direction direction strength in L-C 50% FATT 50% FATTSteel temp. (.degree. C.) (MPa) (MPa) (MPa) (1/4 thickness) (.degree. C.) (1/4 thickness) (.degree. C.) Reference__________________________________________________________________________A 850 598 602 4 -70 -79 Example of the inv. *1A 800 595 598 3 -73 -84 Example of the inv.A 750 586 611 25 -83 -94 Example of the inv.A 700 583 637 54 -88 -100 Example of the inv.B 850 509 510 1 20 0 Conventional exampleB 800 510 512 2 15 -10 Conventional exampleB 750 503 524 21 -10 -25 Conventional exampleB 700 505 525 20 -20 -45 Conventional exampleC 850 613 615 2 5 -30 Comparative exampleC 800 612 615 3 -25 -60 Comparative exampleC 750 607 622 15 -45 -75 Comparative exampleC 700 601 628 27 -64 -95 Comparative__________________________________________________________________________ example *1: Example of the inv. means Example of the invention.
TABLE 2-1__________________________________________________________________________Chemical component (wt %)Symbol Claimedof formulasteel C Si Mn Al Nb B Cu Ni Ti Mo V Cr W Ca REM N P cm *1 Reference__________________________________________________________________________ 1 0.013 -- 1.60 0.033 0.035 0.0013 -- -- 0.01 -- -- -- -- -- -- -- 0.100 296 Example *2 2 0.006 -- 1.80 0.025 0.048 0.0015 -- -- 0.02 -- -- -- -- -- -- -- 0.104 354 Example 3 0.003 0.35 1.80 0.040 0.035 0.0015 0.65 0.35 0.01 -- -- -- -- -- -- -- 0.151 353 Example 4 0.015 0.25 1.55 0.035 0.035 0.0018 0.50 0.25 0.01 -- -- -- -- -- -- -- 0.139 313 Example 5 0.045 0.35 1.80 0.035 0.026 0.0015 0.50 0.25 0.01 -- -- -- -- -- -- -- 0.183 323 Comp. ex. *3 6 0.006 0.80 1.85 0.050 0.010 0.0015 0.20 0.10 0.01 -- -- -- -- -- -- -- 0.144 275 Comp. ex. 7 0.007 0.30 1.22 0.035 0.085 0.0012 0.50 0.25 0.01 -- -- -- -- -- -- -- 0.113 395 Example 8 0.007 0.35 2.25 0.033 0.032 0.0010 0.50 0.25 0.01 -- -- -- -- -- -- -- 0.165 397 Example 9 0.013 0.35 1.55 0.033 0.035 0.0010 0.30 -- 0.01 -- 0.038 -- -- -- -- -- 0.126 306 Example10 0.013 0.35 1.55 0.033 0.035 0.0010 0.30 -- 0.01 -- 0.022 -- -- -- -- -- 0.124 306 Example11 0.025 0.35 1.82 0.033 0.015 0.0010 0.50 -- 0.01 -- -- -- -- -- -- -- 0.158 302 Example12 0.014 0.33 3.21 0.035 0.050 0.0015 0.40 0.20 0.02 -- -- -- -- -- -- -- 0.216 562 Comp. ex.13 0.005 0.30 1.85 0.210 0.008 0.0018 0.65 0.35 0.01 -- -- -- -- -- -- -- 0.155 292 Comp. ex.14 0.006 0.25 1.88 0.040 -- 0.0015 0.20 0.10 0.01 -- -- -- -- -- -- -- 0.128 254 Comp. ex.15 0.008 -- 1.60 0.040 0.015 0.0010 0.50 0.50 0.01 -- -- -- -- -- -- -- 0.126 267 Comp. ex.16 0.007 0.25 0.90 0.035 0.050 0.0013 -- -- 0.01 -- -- -- -- -- -- -- 0.067 242 Comp. ex.17 0.015 0.25 2.05 0.055 0.015 0.0010 3.5 0.5 0.01 -- -- -- -- -- -- -- 0.314 490 Comp.__________________________________________________________________________ ex.
TABLE 2-2__________________________________________________________________________Sym- Chemical component (wt %)bol Claimedof formula Refer-steel C Si Mn Al Nb B Cu Ni Ti Mo V Cr W Ca REM N P cm *1 ence__________________________________________________________________________18 0.007 0.25 1.85 0.030 0.033 0.0015 0.3 0.1 0.30 -- -- -- -- -- -- -- 0.130 335 Comp. ex.19 0.014 0.28 1.60 0.040 0.028 -- -- 0.2 0.01 -- -- -- -- -- -- -- 0.106 276 Comp. ex.20 0.006 0.30 1.78 0.025 0.043 0.0010 1.2 0.6 0.01 -- -- -- -- -- 0.006 -- 0.180 397 Exam- ple21 0.007 0.30 1.58 0.030 0.050 0.0015 0.5 0.3 0.03 0.050 -- 0.05 -- -- -- -- 0.139 355 Exam- ple22 0.012 0.01 1.56 0.033 0.055 0.0018 0.25 -- 0.01 -- 0.015 -- -- -- -- -- 0.113 354 Exam- ple23 0.005 0.05 1.55 0.035 0.055 0.0012 0.50 0.25 0.01 -- -- -- 0.05 0.005 -- -- 0.119 363 Exam- ple24 0.018 0.30 1.75 0.040 0.043 0.0055 -- -- 0.01 -- -- -- -- -- -- -- 0.143 335 Comp. ex.25 0.030 0.35 1.35 0.053 -- -- 0.02 0.10 -- 0.075 0.041 0.03 -- -- -- -- 0.122 175 Comp. ex.26 0.008 -- 1.59 0.033 0.065 0.0013 -- -- 0.01 -- 0.115 -- -- -- -- 0.0092 0.106 369 Exam- ple27 0.009 -- 1.80 0.025 0.048 0.0015 -- -- 0.02 -- 0.130 -- -- -- -- 0.0066 0.120 354 Exam- ple28 0.013 0.35 1.80 0.040 0.035 0.0015 0.65 0.35 0.01 -- 0.150 -- -- -- -- 0.0085 0.176 353 Exam- ple29 0.008 0.25 1.82 0.035 0.035 0.0018 0.50 0.25 0.01 -- 0.107 -- -- -- -- 0.0093 0.156 348 Exam- ple30 0.008 0.30 1.22 0.035 0.085 0.0012 0.50 0.25 0.01 -- 0.089 -- -- -- -- 0.0043 0.123 395 Exam- ple31 0.008 0.35 2.25 0.033 0.032 0.0010 0.50 0.25 0.01 -- 0.126 -- -- -- -- 0.0067 0.179 397 Exam- ple32 0.007 0.30 1.78 0.025 0.043 0.0010 1.2 0.6 0.01 -- 0.066 -- -- -- 0.006 0.0080 0.188 397 Exam- ple33 0.008 0.30 1.58 0.030 0.050 0.0015 0.5 0.3 0.03 0.050 0.068 0.05 -- -- -- 0.0035 0.146 355 Exam- ple34 0.014 -- 1.59 0.033 0.055 0.0016 0.35 -- 0.01 -- 0.097 -- 0.05 -- -- 0.0089 0.129 363 Exam- ple35 0.009 0.05 1.55 0.035 0.055 0.0012 0.50 0.25 0.01 -- 0.117 -- -- 0.005 -- 0.0100 0.135 363 Exam- ple__________________________________________________________________________ *1: Claimed formula; 130Mn - 13Ni + 2500Nb + 55Cu *2: Example means Example of the invention. *3: Comp. ex. means Comparative example.
TABLE 3-1__________________________________________________________________________Symbol Heating Thickness Thickness Rolling Finishingof temperature of slab of plate reduction temp. Coolingsteel (.degree. C.) (mm) (mm) ratio (%) (.degree. C.) method__________________________________________________________________________ 1 1150 100 70 30 900 Air cooling 2 1150 100 70 30 800 Air cooling 3 1180 310 100 67.7 800 Air cooling 4 1150 100 50 50 950 Water cooling (3.degree. C./s)4-1 1150 100 50 50 800 Water cooling (15.degree. C./s) 5 1150 100 100 0 -- Air cooling 6 1150 100 30 70 830 Air cooling 7 1150 100 100 0 -- Air cooling 8 1150 100 70 30 830 Water cooling (7.degree. C./s) 9 1150 100 70 30 920 Air cooling10 1150 100 70 30 830 Air cooling11 1150 100 70 30 800 Air cooling12 1150 100 70 30 800 Air cooling13 1150 100 70 30 800 Air cooling14 1150 100 70 30 800 Air cooling15 1150 100 70 30 800 Air cooling16 1150 100 70 30 800 Air cooling17 1150 100 70 30 800 Air cooling__________________________________________________________________________
TABLE 3-2__________________________________________________________________________Symbol Heating Thickness Thickness Rolling Finishingof temperature of slab of plate reduction temp. Coolingsteel (.degree. C.) (mm) (mm) ratio (%) (.degree. C.) method__________________________________________________________________________18 1180 100 70 30 800 Air cooling19 1150 100 70 30 800 Air cooling20 1150 100 70 30 800 Air cooling21 1150 100 70 30 980 Air cooling22 1150 100 70 30 910 Air cooling23 1150 100 70 30 900 Air cooling24 1150 100 70 30 800 Air cooling25 1150 100 70 30 800 Air cooling26 1150 100 70 30 850 Air cooling27 1150 100 70 30 800 Air cooling28 1180 310 100 67.7 800 Air cooling29 1150 100 50 50 800 Water cooling (3.degree. C./s)30 1150 100 50 50 800 Water cooling (15.degree. C./s)31 1150 100 100 0 -- Air cooling32 1150 100 70 30 830 Water cooling (7.degree. C./s)33 1150 100 70 30 800 Air cooling34 1150 100 70 30 980 Air cooling35 1150 100 70 30 850 Air cooling__________________________________________________________________________
TABLE 4-1__________________________________________________________________________ 50% FATT- 50% FATT- Crack TS-L TS-C YS-L YS-C 1/4 .times. t 1/2 .times. t HAZvE-20 preventing MaximumSteel (MPa) (MPa) (MPa) (MPa) (.degree. C.) (.degree. C.) (J) temp. (.degree. C.) hardness Hv .DELTA.Hv Reference__________________________________________________________________________ 1 612 613 472 474 -70 -65 301 20 159 8 Example *1 2 615 617 475 457 -65 -60 297 20 163 10 Example 3 595 600 433 438 -60 -60 310 20 210 7 Example 4 601 605 488 490 -80 -75 304 20 195 12 Example4-1 610 615 495 497 0 5 298 20 197 21 Comp. ex. *2 5 613 615 488 490 20 45 8 20 240 43 Comp. ex. 6 660 662 547 550 -25 5 7 20 220 8 Comp. ex. 7 600 601 453 456 -55 -50 312 20 160 8 Example 8 725 730 610 613 -65 -60 278 20 237 13 Example 9 620 621 482 484 -75 -70 301 20 162 8 Example10 618 620 466 468 -73 -68 321 20 160 6 Example11 631 633 486 490 -66 -66 291 70 159 11 Example12 780 788 668 678 -10 5 18 20 300 18 Comp. ex.13 604 610 470 476 0 30 15 20 230 7 Comp. ex.14 432 430 306 307 -15 10 201 20 223 40 Comp. ex.15 507 510 389 395 -20 5 275 20 171 15 Comp. ex.16 570 572 466 470 -20 10 209 20 161 18 Comp. ex.17 992 1014 951 963 30 60 10 150 420 13 Comp.__________________________________________________________________________ ex.
TABLE 4-2__________________________________________________________________________ 50% FATT- 50% FATT- Crack TS-L TS-C YS-L YS-C 1/4 .times. t 1/2 .times. t HAZvE-20 preventing MaximumSteel (MPa) (MPa) (MPa) (MPa) (.degree. C.) (.degree. C.) (J) temp. (.degree. C.) hardness Hv .DELTA.Hv Reference__________________________________________________________________________18 662 663 553 557 -30 -10 235 20 273 17 Comp. ex.19 480 487 378 383 -40 -15 245 20 207 38 Comp. ex.20 618 622 488 491 -60 -60 324 20 165 11 Example21 610 615 499 504 -60 -55 309 20 172 10 Example22 600 603 479 481 -65 -60 275 20 157 9 Example23 613 617 473 475 -70 -60 295 20 156 12 Example24 612 615 495 498 -60 -25 105 20 270 28 Comp. ex.25 412 410 287 290 10 35 120 70 291 58 Comp. ex.26 622 623 480 482 -79 -73 305 10 183 7 Example27 624 626 482 482 -71 -66 302 10 165 9 Example28 608 613 442 447 -69 -69 315 10 238 6 Example29 618 622 502 504 -88 -83 312 10 214 11 Example30 623 624 471 474 -64 -58 316 10 179 7 Example31 741 746 624 627 -74 -69 282 10 259 12 Example32 630 634 498 501 -68 -68 328 10 191 10 Example33 639 645 523 528 -70 -64 312 10 204 9 Example34 619 622 494 496 -74 -69 280 10 190 8 Example35 624 628 482 484 -78 -67 299 10 156 10 Example__________________________________________________________________________ *2: Example means Example of the invention. *3: Comp. ex. means Comparative example.
EXAMPLE
Thick steel plates were made using steel slabs whose components were variously adjusted as shown in Tables 2-1 and 2-2 according to the conditions shown in Tables 3-1 and 3-2.
The mechanical properties of the thus obtained thick steel plates were investigated by executing a tensile test and a Charpy test. To evaluate the toughness of HAZ, Charpy test pieces were collected after the steel plates were heated to 1400.degree. C. and then subjected to a heat cycle for cooling them from 800.degree. C. to 500.degree. C. in 15 seconds (which corresponded to the heat history of HAZ when a thick steel plate of 50 mm thick was welded with the amount of heat input of 45 kJ/cm) and the Charpy absorbed energy of them was measured at 0.degree. C. A maximum hardness test was executed based on JIS Z3101 after the test pieces were welded at room temperature. Further, to evaluate the variation of strength in the thickness direction of the plates, the variation of hardness of the steel plates in the thickness direction was investigated by measuring the hardness of the cross section of the steel plates at the pitch of 2 mm.
Tables 4-1 and 4-2 shows the result of these investigations. As shown in Tables 4-1 and 4-2, it is found that the thick steel plates obtained according to the present invention have a tensile strength of 570 MPa or more and are excellent in toughness and since they have a uniform microstructure, the variation of hardness in a thickness direction is very small.
The steel products obtained by the present invention have no variation in physical properties or microstructure which would otherwise be caused by the cooling rate used in a cooling process when they are made in an industrial scale. Therefore, it is possible to provide a stable supply on an industrial scale of steel products of high strength and high toughness which have minimal variation of the material in a thickness direction and are excellent in weldability, the demand for which is expected to increase hereinafter. It will be understood that the present invention is also applicable to the field of section steels.
Claims
  • 1. A method of manufacturing a thick steel product of a thickness of at least 50 mm and high strength and high toughness having excellent weldability and minimal variation in microstructure and physical properties, comprising the steps of heating a steel raw material to a temperature in a range from Ac.sub.3 to 1350.degree. C., hot rolling to a thickness of at least 50 mm at a final finishing temperature more than 800.degree. C. and then cooling said steel raw material at a cooling rate of 10.degree. C./sec. or less, wherein said steel raw material comprises a composition containing the following components:
  • C: 0.001-0.025 wt %;
  • Mn: 1.0-3.0 wt %;
  • Ti: 0.005-0.20 wt %;
  • Nb: 0.005-0.20 wt %;
  • B: 0.0003-0.0050 wt %; and
  • Al: 0.01-0.100 wt %
  • balance essentially Fe and incidental impurities, said composition having a transformation start temperature (B.sub.s) of 670.degree. C. or less, wherein said composition satisfies the following formula:
  • 130 Mn+2500 Nb .gtoreq.296 (1).
  • 2. The method according to claim 1, wherein said composition further comprises the following components:
  • V: 0.04-0.15 wt %; and
  • N: 0.0035-0.0100 wt %,
  • wherein said composition further comprises at least one of the following components:
  • REM: 0.02 wt % or less; and
  • Ca: 0.006 wt % or less.
  • wherein said composition further comprises at least one of the following components:
  • Si: 0.60 wt % or less;
  • Cr: 0.2 wt % or less;
  • Ni: 0.05-2.0 wt %;
  • Mo: 0.5 wt % or less;
  • W: 0.5 wt % or less; and
  • Cu: 0.05-0.7 wt %
  • wherein said composition further satisfies the following formula:
  • 130 Mn-13 Ni+2500 Nb+55 Cu.gtoreq.296 (2).
  • 3. The method according to claim 1, wherein said composition further comprises the following components:
  • V: 0.005-0.04 wt %,
  • wherein said composition further comprises at least one of the following components:
  • REM: 0.02 wt % or less; and
  • Ca: 0.006 wt % or less.
  • wherein said composition further comprises at least one of the following components:
  • Si: 0.60 wt % or less;
  • Cr: 0.02 wt % or less;
  • Ni: 0.05-2.0 wt %;
  • Mo 0.5 wt % or less;
  • W: 0.5 wt % or less; and
  • Cu: 0.05-0.7 wt %
  • wherein said composition further satisfies the formula:
  • 130 Mn-13 Ni+2500 Nb+55 Cu.gtoreq.296 (2).
  • 4. The method according to claim 1, wherein said composition further comprises the following components:
  • V: 0.04-0.15 wt %; and
  • N: 0.0035-0.0100 wt %.
  • 5. The method according to claim 1, wherein said composition further comprises the following component:
  • V: 0.005-0.04 wt %.
  • 6. The method according to claim 1, wherein said composition further comprises at least one of the following components:
  • Si: 0.60 wt % or less;
  • Cr: 0.2 wt % or less;
  • Ni: 0.05-2.0 wt %;
  • Mo: 0.5 wt % or less;
  • W: 0.5 wt % or less; and
  • Cu: 0.05-0.7 wt %
  • wherein said composition further satisfies the following formula:
  • 130 Mn-13 Ni+2500 Nb+55 Cu.gtoreq.296 (2).
  • 7.
  • 7. The method according to claim 1, wherein said composition further comprises at least one of the following components:
  • REM: 0.02 wt % or less; and
  • Ca: 0.006 wt % or less.
  • 8. The method according to claim 1, wherein said composition further comprises the following components:
  • V: 0.04-0.15 wt %; and
  • N: 0.0035-0.0100 wt %,
  • wherein said composition further comprises at least one of the following components:
  • Si: 0.60 wt % or less;
  • Cr: 0.2 wt % or less;
  • Ni: 0.05-2.0 wt %;
  • Mo: 0.5 wt % or less;
  • W: 0.5 wt % or less; and
  • Cu: 0.05-0.7 wt %,
  • wherein said composition further satisfies the following formula:
  • 130 Mn-13 Ni+2500 Nb+55 Cu.gtoreq.296 (2).
  • 9. The method according to claim 1, wherein said composition further comprises the following components:
  • V: 0.005-0.04 wt %;
  • wherein said composition further comprises at least one of the following components:
  • Si: 0.60 wt % or less;
  • Cr: 0.2 wt % or less;
  • Ni: 0.05-2.0 wt %;
  • Mo: 0.5 wt % or less;
  • W: 0.5 wt % or less; and
  • Cu: 0.05-0.7 wt %,
  • wherein said composition further satisfies the following formula:
  • 130 Mn-13 Ni+2500 Nb+55 Cu.gtoreq.296 (2).
  • 10. The method according to claim 1, wherein said composition further comprises the following components:
  • V: 0.04-0.15 wt %; and
  • N: 0.0035-0.0100 wt %,
  • wherein said composition further comprises at least one of the following components:
  • REM: 0.02 wt % or less; and
  • Ca: 0.006 wt % or less.
  • 11. The method according to claim 1, wherein said composition further comprises the following components:
  • V: 0.005-0.04 wt %,
  • wherein said composition further comprises at least one of the following components:
  • REM: 0.02 wt % or less; and
  • Ca: 0.006 wt % or less.
Priority Claims (2)
Number Date Country Kind
8-087095 Mar 1996 JPX
8-263805 Sep 1996 JPX
US Referenced Citations (2)
Number Name Date Kind
4219371 Nakasugi et al. Aug 1980
4521258 Tamehiro et al. Jun 1985
Foreign Referenced Citations (8)
Number Date Country
0 733 715 Sep 1996 EPX
6-67621 Apr 1985 JPX
61-67717 Apr 1986 JPX
63-162838 Jul 1988 JPX
4-350127 Dec 1992 JPX
6-220576 Aug 1994 JPX
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2 131 832 Jun 1984 GBX