US20060123949A1

US20060123949A1 - Highly ductile steel sheet and method of manufacturing the same

Info

Publication number: US20060123949A1
Application number: US11/293,359
Authority: US
Inventors: Sei Kimura; Takamitsu Nakasuga
Original assignee: Kobe Steel Ltd
Current assignee: Kobe Steel Ltd
Priority date: 2004-12-09
Filing date: 2005-12-05
Publication date: 2006-06-15
Also published as: DE602005003430T2; CN1786244A; KR100711410B1; KR20060065492A; EP1669471A1; DE602005003430D1; CN100378242C; TWI274077B; TW200632103A; EP1669471B1

Abstract

A steel sheet has a C content in the range of 0.04 to 0.25% by mass, a Si content in the range of 0.05 to 3% by mass, a Mn content in the range of 0.1 to 3% by mass, an Al content in the range of 0.01 to 2% by mass, a P content of 0.02% by mass or below and higher than 0% by mass, and a S content in the range of 0 to 0.005% by mass. The number of CaO.Al₂O₃inclusions containing CaO, Al₂O₃, SiO₂and MgO, having a CaO content of 5% or above, a SiO₂content of 0.1% or above and an Al₂O₃content of 60% or above, respectively, having major axes of 30 μm or above, and contained in 1 kg of the steel sheet is seventy or below. The steel sheet is highly ductile and has high bore-expandability. A steel slab manufacturing method manufactures a steel slab for forming the steel sheet.

Description

BACKGROUND OF THE INVENTION

1. Field of the Invention
The present invention relates to a highly ductile cold-rolled steel sheet having high bore expandability and a method of manufacturing such a highly ductile steel sheet.
2. Description of the Related Art
Steel sheets for forming body frames of automobiles are required to have high ductility represented by bore expandability. Known inclusions adversely affecting the ductility of steel sheets are oxides, such as Al₂O₃, and sulfides, such as MnS. Reduction of the amount of those inclusions contained in steel sheets is important to provide steel sheets with high ductility.
Techniques for improving the ductility of steel sheets disclosed in JP-A Nos. 2000-144230 and 2002-327239 are intended to reduce the number of alumina clusters. A technique disclosed in JP-A No. 2000-1736 forms a highly ductile high-tension steel sheet containing oxide inclusions having a predetermined chemical composition and particle sizes in the range of 1 to 50 μm, and containing at least one of TiO₂, CaO and REM oxide.
Basically, those prior art techniques add Ti as an essential component to the steel sheet to improve the ductility of the steel sheet. However, hard TiN inclusions are produced in the steel sheet in some cases and the hard TiN inclusions deteriorate the ductility of the steel sheet.
A cold-rolled steel sheet disclosed in, for example, JP-A No. 2002-212674, in which Ti is not an essential component, contains Mg. Cracks formed in the edge of a punched hole formed in this prior art steel sheet containing Mg are minute and uniform, which proves that the steel sheet has improved bore expandability. Although those prior art techniques are effective in improving the ductility of steel sheets to some extent, the ductility of steel sheets produced by those prior art techniques is not necessarily as high as ductility required in recent years.

SUMMARY OF THE INVENTION

Accordingly, it is an object of the present invention to provide a highly ductile steel sheet having high bore expandability and a method of manufacturing a highly ductile steel sheet.
A steel sheet in a first aspect of the present invention has a C content in the range of 0.04 to 0.25% by mass, a Si content in the range of 0.05 to 3% by mass, a Mn content in the range of 0.1 to 3% by mass, an Al content in the range of 0.01 to 2% by mass, a P content of 0.02% by mass or below and higher than 0% by mass, and a S content in the range of 0 to 0.005% by mass; wherein the number of CaO.Al₂O₃inclusions containing CaO, Al₂O₃, SiO₂and MgO, having a CaO content of 5% or above, a SiO₂content of 0.1% or above and an Al₂O₃content of 60% or above, respectively having major axes of 30 μm or above, and contained in 1 kg of the steel sheet is seventy or below.
A steel slab manufacturing method in a second aspect of the present invention includes the steps of: producing CaO slag containing CaO, Al₂O₃, SiO₂, MgO, MnO and Fe, and having a CaO content of 45% or above, a total Fe content of 5% or below, and a MnO content of 3% or below on a molten steel decarburized in a decarburizing furnace and contained in a ladle; desulfurizing the molten steel to reduce the S content of the molten steel to 0.005% or below by stirring the molten steel and the CaO slag by a gas stirring method; circulating the desulfurized molten steel in a vacuum circulation degassing apparatus for 10 min or longer; and forming a steel slab by casting the molten steel circulated in the vacuum circulation degassing apparatus.
The steel sheet of the present invention can be produced from the thus produced steel slab.
The present invention reduces the S content of the molten steel effectively to suppress the production of sulfide inclusions by effectively desulfurizing the decarburized molten steel decarburized by the decarburizing furnace by the CaO inclusions of a properly adjusted composition, and reduces oxide inclusions originating from the CaO slag and adversely affecting the ductility of the steel to the least possible extent. A highly ductile steel sheet can be produced by processing the steel slab produced by casting the thus produced molten steel.

DESCRIPTION OF THE PREFERRED EMBODIMENTS

Various inclusions contained in a steel are principal factors that deteriorate the ductility of steel sheets produced by processing the steel and cause cracks when the steel sheet is processed. The reduction of such inclusions will improve the ductility of the steel sheet. When a molten steel having a high S content is cast to produce a steel slab, MnS inclusions precipitate at a stage of the cast molten steel and the MnS precipitated in the steel affects adversely to the ductility of the steel. Thus it is important to suppress the precipitation of MnS so that the ductility of the steel may not be reduced.
The inventors of the present invention found through studies that the precipitation of MnS can be effectively suppressed by reducing the S content of the steel to a value in the range of 0 to 0.005% by mass. Hereinafter, content in “% by mass” will be simply indicated in “%”. From the viewpoint of improving ductility, it is preferable that the S content of the steel is 0.004% or below, more preferably, 0.003% or below.
To reduce the S content of the steel to 0.005% or below, the molten steel needs to be desulfurized in a refining process by mixing desulfurizing slag in the molten steel. The desulfurizing slag may be mixed in the molten steel by any suitable conventional mixing method. For example, the desulfurizing slag may be mixed in the molten steel by a stirring method that blows a gas through a refractory lance into the molten steel to stir the slag and the molten steel or by a stirring method that blows a gas through a plug on the bottom of a ladle into the molten steel to stir the molten steel and the slag.
Desulfurizing slag containing CaO is used generally in the industry. Suitable desulfurizing slag is, for example, CaO, CaO.CaF₂slag, CaO.Al₂O₃slag, CaO.Al₂O₃.CaF₂slag, CaO.Al₂O₃.MgO slag and CaO.Al₂O₃.SiO₂slag. These substances will be inclusively referred to as CaO slag. To form the desulfurizing slag, namely, the CaO slag, on the surface of the molten steel, a CaO flux containing slags above is added to the molten steel. The respective amounts of CaO, total Fe and MnO contained in the slag need to be controlled properly. Suppose that the sum of the respective amounts of CaO, Al₂O₃, SiO₂, MgO, MnO and total Fe (in some cases, referred to as “T.Fe”) is 100% (CaO+Al₂O₃+SiO₂+MgO+MnO+total Fe=100%). Then, the slag needs to have a CaO content of 45% or above. Effective desulfurization of the molten steel cannot be expected if the CaO content of the slag is less than 45%. Preferably, the CaO content of the slag is 48% or above, more preferably, 50% or above. The CaO content of the slag can be adjusted to 45% or above by using a CaO flux having a CaO content of 50% or above.
The slag formed on the surface of the molten steel contained in the ladle contains FeO and MnO produced in the molten steel during refining in an oxidation refining furnace, such as a converter or an electric furnace. The desulfurizing effect of the slag decreases if the slag contains an excessive amount of T.Fe content and an excessive amount of MnO. Therefore the respective amounts of T.Fe content and MnO contained in the slag must be properly adjusted. The respective amounts of T.Fe and MnO must be 5.0% or below and 3% or below, respectively, when containing CaO+Al₂O₃+SiO₂+MgO+MnO+total Fe=100%. Preferably, the amount of T.Fe contained in the slag is 4% or below and the amount of MnO contained in the slag is 2% or below. A recommended T.Fe content and a recommended MnO content of the slag are 3% or below and 1% or below, respectively. In order to reduce the slag to adjust the T.Fe content and the MnO content of the slag to values in the foregoing ranges, slag produced during refining in the oxidation refining furnace is removed before the desulfurizing flux is added to the molten steel or Al, Si and C are added to the molten steel or the slag or to either of the molten steel and the slag.
The foregoing desulfurizing process eliminates MnS inclusions that reduce the ductility of the steel sheet. However, inclusions originating in the desulfurizing slag (hereinafter, referred to as “slag inclusions”) and produced in the molten steel when the molten steel and the slag are stirred for ladle refining remain in the molten steel when the molten steel is cast to produce a steel slab. The slag inclusions contained in the steel slab reduce the ductility of steel sheets formed by rolling the steel slab.
The slag inclusions are identified by the following condition. The ladle slag has a CaO content of 45% or above and a SiO₂content of below 10%. When the ladle slag and the molten steel are mixed by stirring, the ladle slag reacts with Al contained in the molten steel and changes into a slag containing CaO, Al₂O₃, SiO₂and MgO, and having a CaO content of 5% or above and a SiO₂content of 0.1% or above (when containing CaO+Al₂O₃+SiO₂+MgO =100%). Such a slag is regarded as slag inclusions. The present invention deals with CaO.Al₂O₃inclusions. The CaO.Al₂O₃inclusions contain CaO, Al₂O₃, SiO₂and MgO and have a CaO content of 5% or above and an Al₂O₃content of 60% or above. Thus the following description will be made on an assumption that the CaO.Al₂O₃inclusions contain CaO, Al₂O₃, SiO₂and MgO, and has a CaO content of 5% or above, a SiO₂content of 0.1% or above and an Al₂O₃content of 60% or above.
The inventors of the present invention made studies of the effect of the CaO.Al₂O₃inclusions contained in steel sheets on the ductility of the steel sheets and found that the CaO.Al₂O₃inclusions having a major axis of 30 μm or above affect the ductility of the steel sheets and the reduction of the number of the CaO.Al₂O₃inclusions contained in 1 kg of the steel sheet to 70 or below, preferably, 60 or below, more preferably 50 or below improves the ductility of the steel sheets remarkably.
A vacuum circulation degassing process (hereinafter, referred to as “RH process”) needs to be executed after the desulfurization process to reduce the amount of the slag inclusions produced by the desulfurization process and contained in the steel by flotative separation. A vacuum circulation degassing apparatus needs to continue the RH process at 10 min or longer to remove the slag inclusions by flotative separation. Preferably, the duration of the RH process is 15 minor longer, more preferably, 20 min or longer.
The present invention provides a highly ductile steel sheet of, for example, a thickness in the range of about 1 to about 3 mm by hot-rolling or cold-rolling a steel slab produced by casting the molten steel processed by the desulfurization process and the RH process. The highly ductile steel sheet can be produced from the foregoing steel slab regardless of the method and conditions of rolling. The chemical composition of the steel needs to be properly adjusted. The ranges of chemical component contents of the steel of the present invention other than S content are determined for the following reasons.
C Content: 0.04 to 0.25%
Although the smaller C content is desirable to improve the ductility, particularly, bore expandability of the steel sheet, the strength of the steel sheet decreases significantly when the carbon content is less than 0.04%. When the C content is higher than 0.25% and the Mn content is in the range specified below, pearlite grains occur excessively, the lamellar intervals of the pearlite grains widens and the balance between strength and local ductility is deteriorated. Therefore, the C content of the steel sheet of the present invention must be in the range of 0.04 to 0.25%. A preferable lower limit C content is on the order of 0.05% and a preferable upper limit C content is on the order of 0.22%.
Si Content: 0.05 to 3%
Si is a useful effective solid solution strengthening element. The Si content of the steel sheet needs to be 0.05% or above to make Si exercise the solid solution strengthening effect. The solid solution strengthening effect of Si saturates at a certain Si content and hence an excessively high Si content is economically disadvantageous. An excessively high Si content will enhance the hot brittleness of the steel sheet. Thus the Si content must be 3% or below. A preferable lower limit of the Si content is 0.1%, more preferably, 0.2% or above. A preferable upper limit of the Si content is 2.5%, more preferably, 2% or below.
Mn Content: 0.1 to 3%
Manganese contained in the steel sheet stabilizes the austenitic phase, facilitates formation of a hard phase during cooling and strengthens the steel sheet. The hard phase necessary for strengthening the steel sheet cannot be formed if the Mn content is excessively low. Therefore, the Mn content must be 0.1% or above. Banded structures develop and the ductility decreases if the Mn content is excessively high. Therefore, an upper limit Mn content must be 3%. Preferably, a lower limit Mn content is 0.2%, more preferably, 0.3% or above. Preferably, an upper limit Mn content is 2.8%, more preferably, 2.5% or below.
Al Content: 0.01 to 2%
Aluminum is necessary for the deoxidation of the molten steel and is effective in promoting desulfurization during ladle refining by lowering the potential of oxygen in the molten steel. The Al content must be 0.01% or above to make such an effect of Al effective. Preferably, the Al content is 0.015%, more preferably, 0.02% or above. The effect of the Al content saturates at a certain Al content and hence an excessively high Al content is economically disadvantageous. Therefore, the Al content must be 2% or below, preferably, 1.5% or below.
P Content: 0.02% or below and higher than 0%
Phosphorus strengthens the steel and, at the same time, embrittles the steel and deteriorates the ductility of the steel. An upper limit P content must be 0.02%, preferably, 0.015%. The effect of P increases with the increase of the P content. Preferably, the P content is 0.003% or above, more preferably, 0.005% or above to make the effect of P effective.
The molten steel contains, in addition to the foregoing basic component elements, Fe and unavoidable impurities, such as Cr, Cu and Sn. When necessary, the steel sheet may contain additional trace elements, such as Mo, V and Nb, in contents in the range of about 0.01 to about 0.05%.
Examples of the steel sheet of the present invention will be described. However, the examples are intended to illustrate the invention and are not to be construed to limit the scope of the invention. Naturally, various changes and variations may be made in the examples specifically described herein without departing from the scope and spirit of the invention.

EXAMPLES

Two hundred and fifty tons of a molten steel decarburized in a converter was tapped from the converter into a ladle. Various alloy steels were added to the molten steel by a ladle refining apparatus to adjust the chemical composition of the molten steel to a predetermined chemical composition and the molten steel was desulfurized. Table 1 shows the respective compositions of desulfurizing slag. Argon gas (Ar gas) was blown through the lance into the molten steel to stir the molten steel. The ladle was carried to a vacuum circulation degassing apparatus after the completion of the composition adjustment and desulfurization. The molten steel was circulated for the RH process by the vacuum circulation degassing apparatus. RH process times, namely, times of duration of the RH process, are shown in Table 1. Molten steels in Examples 3 and 4 were not processed by ladle refining and molten steels in Examples 5 and 6 were not processed by the RH process.

TABLE 1


Molten steel processing
process	RH	Composition of desulfurizing slag for ladle refining

Sample

Ladle

RH

processing

(% by mass)

No.	refining	process	time (min)	CaO	Al₂O₃	SiO₂	MgO	T. Fe	MnO	Total

1	◯	◯	13	51.8	26.2	8.5	7.1	5.2	1.2	100
2	◯	◯	25	46.1	29.5	8.2	8.1	2.5	5.6	100
3	◯	◯	17	39.5	36.8	8.1	9.0	2.5	4.1	100
4	X	◯	15	—	—	—	—	—	—	100
5	X	◯	19	—	—	—	—	—	—	100
6	◯	X	—	53.1	31.3	6.2	7.1	1.1	1.2	100
7	◯	X	—	53.7	31.8	5.8	6.5	0.8	1.4	100
8	◯	◯	7	49.9	34.4	4.8	7.5	1.5	1.9	100
9	◯	◯	11	46.7	33.7	6.2	9.7	2.1	1.6	100
10	◯	◯	15	48.2	36.1	5.1	8.2	1.1	1.3	100
11	◯	◯	18	53.2	37.1	4.2	3.6	0.9	1.0	100
12	◯	◯	23	57.5	31.0	3.4	5.5	1.2	1.4	100

Steel slabs were produced by casting the molten steels processed by the RH process by a continuous casting process. The steel slabs were subjected to a hot rolling process to produce hot-rolled steel sheets of a thickness in the range of 3 to 4 mm. The hot-rolled steel sheets were subjected to a cold rolling process to produce cold-rolled steel sheets of a thickness in the range of 2 to 3 mm.
Sample pieces for a bore expand test were sampled form the cold-rolled steel sheets. The sample pieces were tested by the flowing test method to evaluate their bore expandability. The number of CaO.Al₂O₃inclusions contained in the steel sheets was determined by the following counting method.
Bore-Expandability
The sample pieces were punched to form bores of 10 mm in diameter therein and the punched sample pieces were subjected to a bore expand test. In the bore expand test, the bore of the sample piece was expanded by pressing a conical punch having a point angle of 60° into the bore, and the diameter of the thus expanded bore was measured when cracks extending through the thickness of the sample piece were formed in the edge of the bore. A limit bore expandability λ was calculated by using an expression:
λ(%)={(D ₁ /D ₀)/D ₀}×100
where D₀is the initial diameter of the bore and D₁is the diameter of the expanded bore. Steel sheets having higher ductility have higher limit bore expandability.
Number of CaO.Al₂O₃Inclusions
Inclusions contained in the cold-rolled steel sheet were extracted by a method disclosed in JP-A No. 2002-340885. The cold-rolled steel sheet was heated and held at 1000° C. for 30 min and then the steel sheet was cooled rapidly for a solution heat treatment to eliminate carbides from the steel sheet. Eight sample pieces of 3.2 mm×100 mm×50 mm each having a weight of 1 kg were cut out from the cold-rolled steel sheet. Each sample piece was immersed in a ferrous chloride solution of pH 6.0 to dissolve 1 kg of iron matrix by a constant-current electrolysis method. Then, the solution was filtered by a filter having pores of 27 μm in diameter to obtain a residue containing CaO inclusions. The number of CaO.Al₂O₃inclusions containing CaO, Al₂O₃, SiO₂and MgO, having a CaO content of 5% or above, a SiO₂content of 0.1% or above and an Al₂03 content 60% or above, respectively having major axes of 30 μm or above and contained in the residue was counted by using a scanning electron microscope combined with a wavelength dispersive x-ray spectrometer (SEM•WDS).

Table 2 shows the counted numbers of CaO.Al₂O₃inclusions and the chemical composition of the steel sheets.

TABLE 2


		Number of CaO.Al₂O₃	Bore
Sample	Chemical composition of steel sheet (% by mass)	inclusions per 1 kg	expandability

No.	C	Si	Mn	P	S	Al	of steel sheet	(%)

1	0.04	1.05	2.17	0.006	0.006	0.025	37	71
2	0.14	0.98	2.10	0.011	0.008	0.014	22	77
3	0.11	1.22	2.46	0.009	0.007	0.038	32	81
4	0.08	1.45	2.25	0.010	0.009	0.027	40	58
5	0.08	1.31	2.41	0.010	0.007	0.031	35	83
6	0.07	1.65	1.51	0.010	0.001	0.034	96	68
7	0.16	1.52	2.23	0.013	0.002	0.027	89	49
8	0.09	0.07	0.82	0.005	0.001	0.029	81	90
9	0.15	0.52	1.28	0.009	0.004	0.028	63	113
10	0.06	0.73	1.57	0.012	0.003	0.047	46	126
11	0.17	1.35	2.16	0.010	0.002	0.036	19	131
12	0.13	0.95	2.00	0.006	0.004	0.044	34	120

It is known from the measured data shown in Table 2 that Samples 9 to 12 meet all the requirements of the present invention. The numbers of the CaO.Al₂O₃inclusions contained in Samples 9 to 12 are small and the Samples 9 to 12 have high bore expandability.
Each of Samples 1 to 8 does not meet some of the requirements of the present invention and has low bore expandability. As regards Samples 1 to 5, although processing time for processing the steel sheet by the RH process is within a range specified by the present invention and the numbers of CaO.Al₂O₃inclusions are within a range required by the present invention, the composition of the desulfurizing slag used by ladle refining does not meet conditions specified by the present invention (Samples 1 to 3) or the molten steel was not processed by ladle refining (Samples 4 and 5). Consequently, the steel sheets in Samples 1 to 8 have a large S content and a low ductility.
The composition of the desulfurizing slag for the ladle refining of the molten steels for forming the steel sheets in Samples 6 to 8 meet requirements of the present invention and have S contents of 0.0055 or below, respectively. However, the molten steels for forming the steel sheets in Samples 6 and 7 are not processed by the RH process after ladle refining and the molten steels for forming the steel sheet in Sample 8 were processed by the RH process for a time shorter than 10 min. Therefore, the numbers of CaO.Al₂O₃inclusions contained in 1 kg of the steel sheets in Samples 6 to 8 are greater than seventy and deteriorates bore expandability.
Although the invention has been described in its preferred embodiments with a certain degree of particularity, obviously many changes and variations are possible therein. It is to be understood that the present invention may be practiced otherwise than as specifically described herein without departing from the scope and spirit thereof.

Claims

1. A steel sheet having a C content in the range of 0.04 to 0.25% by mass, a Si content in the range of 0.05 to 3% by mass, a Mn content in the range of 0.1 to 3% by mass, an Al content in the range of 0.01 to 2% by mass, a P content of 0.02% by mass or below and higher than 0% by mass, and a S content in the range of 0 to 0.005% by mass;

wherein the number of CaO.Al₂O₃inclusions containing CaO, Al₂O₃, SiO₂and MgO, contain 5% or above of CaO, 0.1% or above of SiO₂and 60% or above of Al₂O₃in 100% of oxides including CaO, Al₂O₃, SiO₂and MgO and having major axes of 30 μm or above, and contained in 1 kg of the steel sheet is seventy or below.

2. The steel sheet according to claim 1, wherein the S content is in the range of 0 to 0.003% by mass.

3. A method of manufacturing a steel slab for forming the steel sheet according to claim 1, said method comprising the steps of:

producing CaO slag containing CaO, Al₂O₃, SiO₂, MgO, MnO and total Fe, and having a CaO content of 45% or above, a total Fe content of 5% or below, and a MnO content of 3% or below on a molten steel decarburized in a decarburizing furnace and contained in a ladle by adding a CaO flux to the molten steel;

desulfurizing the molten steel to reduce the S content of the molten steel to 0.005% or below by stirring the molten steel and the CaO slag by a gas stirring method in the ladle;

circulating the desulfurized molten steel contained in the ladle in a vacuum circulation degassing apparatus for 10 min or longer; and

forming a steel slabby casting the molten steel circulated in the vacuum circulation degassing apparatus.

4. The method according to claim 3, the CaO slag has a CaO content of 50% by mass or above.

5. The method according to claim 3, wherein the CaO slag has a MnO content of 2% by mass or blow and a total Fe content of 3% by mass or below.