CA2832357C - A steel sheet suitable for enamelling and method for producing such a sheet - Google Patents
A steel sheet suitable for enamelling and method for producing such a sheet Download PDFInfo
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- CA2832357C CA2832357C CA2832357A CA2832357A CA2832357C CA 2832357 C CA2832357 C CA 2832357C CA 2832357 A CA2832357 A CA 2832357A CA 2832357 A CA2832357 A CA 2832357A CA 2832357 C CA2832357 C CA 2832357C
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- 229910000831 Steel Inorganic materials 0.000 title claims abstract description 64
- 239000010959 steel Substances 0.000 title claims abstract description 64
- 238000004519 manufacturing process Methods 0.000 title claims abstract description 7
- 239000012535 impurity Substances 0.000 claims abstract description 15
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 13
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 12
- 238000000034 method Methods 0.000 claims description 35
- 238000000137 annealing Methods 0.000 claims description 28
- 239000000203 mixture Substances 0.000 claims description 18
- 210000003298 dental enamel Anatomy 0.000 claims description 15
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 6
- 238000005097 cold rolling Methods 0.000 claims description 6
- 238000005098 hot rolling Methods 0.000 claims description 6
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 5
- 229910001873 dinitrogen Inorganic materials 0.000 claims description 3
- 239000010960 cold rolled steel Substances 0.000 claims description 2
- 238000005261 decarburization Methods 0.000 description 19
- 238000002791 soaking Methods 0.000 description 12
- 230000015572 biosynthetic process Effects 0.000 description 7
- 239000010949 copper Substances 0.000 description 7
- 241000251468 Actinopterygii Species 0.000 description 6
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 5
- 239000011575 calcium Substances 0.000 description 5
- 229910052760 oxygen Inorganic materials 0.000 description 5
- 239000001301 oxygen Substances 0.000 description 5
- 229910052720 vanadium Inorganic materials 0.000 description 5
- 229910052796 boron Inorganic materials 0.000 description 4
- 229910052802 copper Inorganic materials 0.000 description 4
- 238000005275 alloying Methods 0.000 description 3
- 229910052791 calcium Inorganic materials 0.000 description 3
- 229910001567 cementite Inorganic materials 0.000 description 3
- 238000010304 firing Methods 0.000 description 3
- 238000001336 glow discharge atomic emission spectroscopy Methods 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- KSOKAHYVTMZFBJ-UHFFFAOYSA-N iron;methane Chemical compound C.[Fe].[Fe].[Fe] KSOKAHYVTMZFBJ-UHFFFAOYSA-N 0.000 description 3
- 229910052717 sulfur Inorganic materials 0.000 description 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 230000032683 aging Effects 0.000 description 2
- YUZILKLGVPUFOT-YHPRVSEPSA-L disodium;5-[(6-anilino-4-oxo-1h-1,3,5-triazin-2-yl)amino]-2-[(e)-2-[4-[(6-anilino-4-oxo-1h-1,3,5-triazin-2-yl)amino]-2-sulfonatophenyl]ethenyl]benzenesulfonate Chemical compound [Na+].[Na+].C=1C=C(\C=C\C=2C(=CC(NC=3NC(NC=4C=CC=CC=4)=NC(=O)N=3)=CC=2)S([O-])(=O)=O)C(S(=O)(=O)[O-])=CC=1NC(N1)=NC(=O)N=C1NC1=CC=CC=C1 YUZILKLGVPUFOT-YHPRVSEPSA-L 0.000 description 2
- 239000002320 enamel (paints) Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 238000010438 heat treatment Methods 0.000 description 2
- 238000005259 measurement Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 229910001208 Crucible steel Inorganic materials 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 229910021386 carbon form Inorganic materials 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 238000004534 enameling Methods 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- 238000000691 measurement method Methods 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 238000004088 simulation Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/004—Very low carbon steels, i.e. having a carbon content of less than 0,01%
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0247—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment
- C21D8/0257—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips characterised by the heat treatment with diffusion of elements, e.g. decarburising, nitriding
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D3/00—Diffusion processes for extraction of non-metals; Furnaces therefor
- C21D3/02—Extraction of non-metals
- C21D3/04—Decarburising
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D8/00—Modifying the physical properties by deformation combined with, or followed by, heat treatment
- C21D8/02—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips
- C21D8/0205—Modifying the physical properties by deformation combined with, or followed by, heat treatment during manufacturing of plates or strips of ferrous alloys
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/46—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D9/00—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor
- C21D9/52—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for wires; for strips ; for rods of unlimited length
- C21D9/54—Furnaces for treating strips or wire
- C21D9/56—Continuous furnaces for strip or wire
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/002—Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/04—Ferrous alloys, e.g. steel alloys containing manganese
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/16—Ferrous alloys, e.g. steel alloys containing copper
Abstract
The present invention is related to a rolled steel sheet suitable for enamelling, said sheet having a carbon profile, defined by a gradient in the C-level from a level Csurface at least one surface of the sheet, to a level Cbulk in the bulk of the sheet, Cbulk being higher than Csurface, and With I - Cbulk higher than 0 and lower than or equal to 0.08wt%, - CsurfaCe between 0 and 0.015wt%, - A1 between 0.012wt% and 0.07wt%, Mn between 0.12wt% and 0.45wt%, 0 lower than 0.01wt% and optionally : - Cu between 0.025wt% and 0.1wt%, - S between 0.008wt% and 0.04wt%, - Ca between 0.0005wt% and 0.005wt%, the balance being Fe and incidental impurities, and wherein the depth where the C-level reaches (Cbulk+Csurface) 12, is higher than 75µm. The invention is equally related to a method for producing said steel sheet.
Description
A STEEL SHEET SUITABLE FOR ENAMELLING AND METHOD FOR
PRODUCING SUCH A SHEET
Field of the Invention [0001] The present invention is related to a steel sheet suitable for enamelling, and to a method for the superficial decarburization of a steel sheet, as a preparation for enamelling the steel.
State of the art.
PRODUCING SUCH A SHEET
Field of the Invention [0001] The present invention is related to a steel sheet suitable for enamelling, and to a method for the superficial decarburization of a steel sheet, as a preparation for enamelling the steel.
State of the art.
[0002] The carbon level of a steel sheet has an important influence on the results in terms of surface quality of an enamel layer applied on the surface of the sheet. A high carbon level at the steel surface may give rise to CO-gas bubble formation, which shows up as black spots and craters in the enamel surface. On the other hand, when a sufficiently high carbon level is present initially in the bulk, this carbon forms coarse cementite during hot rolling which cracks upon cold rolling. These cracks are capable of capturing hydrogen which enters the steel during the enamelling process. When hydrogen is insufficiently captured, pressure will rise at the steel/enamel surface which gives rise to the so-called 'fish-scale' deformation of the enamel.
[0003] It is therefore advantageous to decarburize the steel only in a layer at the surface of the steel, i.e.
to conduct a superficial decarburization. Document JP-A-2282421 describes such a method, wherein a continuously cast and annealed non-aging steel sheet for enamelling is produced, characterized in that a continuous-cast steel slab containing C between 0.0025 and 0.0050wt%, Si max.
0.03wt%, Mn between 0.1 and 0.6wt%, P between 0.005 and 0.03wt%, S between 0.005 and 0.03wt%, Al max. 0.01wt%, N
max. 0.004wt%, Cu between 0.01 and 0.06wt%, 0 between 0.02 and 0.06wt%, V between 0.01 and 0.06wt%, the balance Fe and inevitable impurities, is hot-rolled with a finishing temperature higher than or equal to 800 C, and a coiling temperature of 600-800 C, cold-rolled with a reduction ratio higher than or equal to 60% and subjected to a decarburization annealing at 700-900 C for 30sec-3min, carried out in a continuous annealing furnace having a decarburizing atmosphere composed of 1-20% water vapour, gaseous hydrogen in an amount higher than or equal to twice the water vapour amount, and the balance being mainly gaseous nitrogen, so as to reduce the C-level to be less than or equal to 0.002wt%. JP-A-6116634 describes a similar method, but wherein the starting material has no vanadium and the initial C level is up to 0.015wt% and B is added instead of V for H-trapping.
to conduct a superficial decarburization. Document JP-A-2282421 describes such a method, wherein a continuously cast and annealed non-aging steel sheet for enamelling is produced, characterized in that a continuous-cast steel slab containing C between 0.0025 and 0.0050wt%, Si max.
0.03wt%, Mn between 0.1 and 0.6wt%, P between 0.005 and 0.03wt%, S between 0.005 and 0.03wt%, Al max. 0.01wt%, N
max. 0.004wt%, Cu between 0.01 and 0.06wt%, 0 between 0.02 and 0.06wt%, V between 0.01 and 0.06wt%, the balance Fe and inevitable impurities, is hot-rolled with a finishing temperature higher than or equal to 800 C, and a coiling temperature of 600-800 C, cold-rolled with a reduction ratio higher than or equal to 60% and subjected to a decarburization annealing at 700-900 C for 30sec-3min, carried out in a continuous annealing furnace having a decarburizing atmosphere composed of 1-20% water vapour, gaseous hydrogen in an amount higher than or equal to twice the water vapour amount, and the balance being mainly gaseous nitrogen, so as to reduce the C-level to be less than or equal to 0.002wt%. JP-A-6116634 describes a similar method, but wherein the starting material has no vanadium and the initial C level is up to 0.015wt% and B is added instead of V for H-trapping.
[0004]
Both prior art methods result in fully or superficially decarburized steel sheets which are suitable for enamelling by Direct White Enamelling (DWE), wherein one white enamel coating is applied on the surface, followed by one firing step. As the initial carbon level is quite low, fish-scale resistance due to cementite formation is not achieved. To compensate for this, a steel with a high oxygen level and a limited Al-level is used in the prior art together with specific alloying elements such as B, V. Thanks to the limited Al-content, oxides of Si and Mn and nitrides of B and V are formed within the bulk of the steel which are beneficial against fish-scaling.
However, this alloying involves extra costs and leads to some technical difficulties, e.g. involving casting with V.
Furthermore, the prior art decarburized sheets have rather low formability as testified by the values of the Lankford coefficient (rm). These values do not exceed 1.8 which is a concern when deep-drawing is foreseen. In particular, figure 1 of JP6116634 shows that rm values between 1.6 and 1.8 are only achieved for a very narrow range of carbon level before decarburizing annealing. Below 0.0050wt%C and above 0.0150wt%C, the rm value is deteriorated.
Both prior art methods result in fully or superficially decarburized steel sheets which are suitable for enamelling by Direct White Enamelling (DWE), wherein one white enamel coating is applied on the surface, followed by one firing step. As the initial carbon level is quite low, fish-scale resistance due to cementite formation is not achieved. To compensate for this, a steel with a high oxygen level and a limited Al-level is used in the prior art together with specific alloying elements such as B, V. Thanks to the limited Al-content, oxides of Si and Mn and nitrides of B and V are formed within the bulk of the steel which are beneficial against fish-scaling.
However, this alloying involves extra costs and leads to some technical difficulties, e.g. involving casting with V.
Furthermore, the prior art decarburized sheets have rather low formability as testified by the values of the Lankford coefficient (rm). These values do not exceed 1.8 which is a concern when deep-drawing is foreseen. In particular, figure 1 of JP6116634 shows that rm values between 1.6 and 1.8 are only achieved for a very narrow range of carbon level before decarburizing annealing. Below 0.0050wt%C and above 0.0150wt%C, the rm value is deteriorated.
[0005]
Summary of the invention
Summary of the invention
[0006] The invention is related to steel sheets and products and to a production method as disclosed below.
The invention is related to a rolled steel sheet suitable for enamelling, said sheet having a carbon profile, defined by a gradient in the C-level from a level Csurface at at least one surface of the sheet, to a level Cbulk in the bulk of the sheet, Cbuik being higher than Csurface and with :
- Cbuik higher than 0 and lower than or equal to 0.08wt%, ¨ Csurface between 0 and 0.015wt%, - Al between 0.012wt% and 0.07wt%, - Mn between 0.12wt% and 0.45wt%, - 0 lower than 0.01wt%
and optionally :
- Cu between 0.025wt% and 0.1wt%, - S between 0.008wt% and 0.04wt%, ¨ Ca between 0.0005wt% and 0.005wt%
the balance being Fe and incidental impurities, and wherein the depth where the C-level reaches (Cmulk+Csurface) /2, is higher than 75 m.
The invention is related to a rolled steel sheet suitable for enamelling, said sheet having a carbon profile, defined by a gradient in the C-level from a level Csurface at at least one surface of the sheet, to a level Cbulk in the bulk of the sheet, Cbuik being higher than Csurface and with :
- Cbuik higher than 0 and lower than or equal to 0.08wt%, ¨ Csurface between 0 and 0.015wt%, - Al between 0.012wt% and 0.07wt%, - Mn between 0.12wt% and 0.45wt%, - 0 lower than 0.01wt%
and optionally :
- Cu between 0.025wt% and 0.1wt%, - S between 0.008wt% and 0.04wt%, ¨ Ca between 0.0005wt% and 0.005wt%
the balance being Fe and incidental impurities, and wherein the depth where the C-level reaches (Cmulk+Csurface) /2, is higher than 75 m.
[0007] According to a preferred embodiment, the steel sheet of the invention has an rm value between 1.8 and 2.1.
[0008] According to specific embodiments, Csurface is between 0.005wt% and 0.015wt%, or between 0 and 0.005wt%.
[0009] According to other specific embodiments, Cbulk is between 0.02wt% and 0.08wt%, or between 0.025wt% and 0.08wt% or between 0.025wt% and 0.06wt%.
[0010] According to another embodiment, the Al-level is between 0.02wt% and 0.06wt%.
[0011] According to a further embodiment, said depth is between 130 m and 200 m.
[0012] The invention is equally related to an enamelled steel sheet consisting of a steel sheet according to any of the above paragraphs, provided with an enamel layer.
[0013] The invention is further related to a steel product produced from a sheet according to the invention, and to an enamelled steel product consisting of a such a product, provided with an enamel layer.
[0014] The invention is also related to a method for producing a rolled steel sheet for enamelling, comprising the steps of :
¨ subjecting a steel slab to hot rolling followed by coiling, and cold rolling, so as to obtain a cold-rolled steel sheet, said slab comprising the following initial composition :
¨ C between 0.02wt% and 0.08wt%, ¨ Al between 0.012wt% and 0.07wt%, ¨ Mn between 0.12wt% and 0.45wt%, ¨ 0 lower than 0.01wt%
and optionally :
¨ Cu between 0.025wt% and 0.1wt%, 5 ¨ S between 0.008wt% and 0.04wt%, ¨ Ca between 0.0005wt% and 0.005wt%, ¨ the balance being Fe and incidental impurities, ¨ subjecting said cold-rolled sheet to continuous annealing step, wherein said sheet is exposed during a decarburizing time to a decarburizing atmosphere comprising water vapour and hydrogen gas, wherein the H2 content is between 1vol% and 95vo1%, the H20 content between 0.04vol% and 33vo1%, the remainder being mainly nitrogen gas, the ratio pH20/pH2 being between 0.04 and 0.5.
¨ subjecting a steel slab to hot rolling followed by coiling, and cold rolling, so as to obtain a cold-rolled steel sheet, said slab comprising the following initial composition :
¨ C between 0.02wt% and 0.08wt%, ¨ Al between 0.012wt% and 0.07wt%, ¨ Mn between 0.12wt% and 0.45wt%, ¨ 0 lower than 0.01wt%
and optionally :
¨ Cu between 0.025wt% and 0.1wt%, 5 ¨ S between 0.008wt% and 0.04wt%, ¨ Ca between 0.0005wt% and 0.005wt%, ¨ the balance being Fe and incidental impurities, ¨ subjecting said cold-rolled sheet to continuous annealing step, wherein said sheet is exposed during a decarburizing time to a decarburizing atmosphere comprising water vapour and hydrogen gas, wherein the H2 content is between 1vol% and 95vo1%, the H20 content between 0.04vol% and 33vo1%, the remainder being mainly nitrogen gas, the ratio pH20/pH2 being between 0.04 and 0.5.
[0015] According to a preferred embodiment, said continuous annealing takes place at an anneal temperature between 760 C and 850 C, and during a decarburizing time between 45s and 300s.
[0016] According to a specific embodiment, the anneal temperature is between 800 C and 850 C.
[0017] According to specific embodiments of the method of the invention, the initial C-level is between 0.025wt% and 0.08wt% or between 0.025wt% and 0.06wt%.
[0018] According to a further embodiment, the initial Al-level is between 0.02wt% and 0.06wt%.
[0019] According to a specific embodiment, the ratio pH20/pH2 is between 0.04 and 0.25.
[0020] The method of the invention may further comprise an over-ageing step at a temperature between 350 C
and 450 C during a timespan between 100s and 500s. The method may further comprise a skinpass step with a reduction of between 0.3% and 1.5%.
Brief description of the figures
and 450 C during a timespan between 100s and 500s. The method may further comprise a skinpass step with a reduction of between 0.3% and 1.5%.
Brief description of the figures
[0021]
Figure 1 illustrates the carbon profile in a steel sheet according to the invention.
Figure 1 illustrates the carbon profile in a steel sheet according to the invention.
[0022]
Figure 2 illustrates an example of an annealing step usable in the method of the invention.
Detailed description of the invention
Figure 2 illustrates an example of an annealing step usable in the method of the invention.
Detailed description of the invention
[0023] The steel sheet of the invention has a C-profile, defined by a gradient in the C-level from a lower value Csurface at the surface to a higher value Cbulk in the bulk. The sheet is obtainable by a method which includes a continuous decarburization step, as will be described further in this text. Figure 1 illustrates the carbon-distribution across the thickness of two sheets according to the invention, with a thickness of 0.7mm. Curve 10 illustrates a sheet which comprises a bulk portion 11, where the C-level Cbulk is substantially constant, and two surface portions 12 (one on each side of the sheet), each surface portion exhibiting the C-profile. The surface level is defined as the minimum value of the C-profile, measured by a suitable measurement technique (e.g. Glow Discharge Optical Emission Spectroscopy (GD-OES), which allows composition measurement as depth analysis). In a steel sheet according to the invention, the C-level at the surface is maximum 0.015wt%, whereas Cbulk is higher than zero and lower than or equal to 0.08wt%. At the same time, Cbulk is higher than Csurface = According to an embodiment, Csurface is between 0.005wt% and 0.015wt%. According to another embodiment, Cõr fa, is between 0 and 0.005wt%.
[0024]
Curve 10 is an example of a sheet where the decarburization has not taken place over the entire thickness of the sheet. This means that the level Cbulk is equal to the initial C-level applied in the production method (described further in more detail).
According to embodiments which correspond to embodiments of the method of the invention (see further), Cbulk is then between 0.02wt% and 0.08wt%, or between 0.025wt% and 0.08wt, or between 0.025wt% and 0.06wt% or between 0.025wt% and 0.05wt%.
Curve 13 illustrates the case where decarburization has continued until the middle plane of the sheet. In this case, Cbulk is smaller than the initial C-level of the method, and the C-profile extends over each half-width of the sheet.
Curve 10 is an example of a sheet where the decarburization has not taken place over the entire thickness of the sheet. This means that the level Cbulk is equal to the initial C-level applied in the production method (described further in more detail).
According to embodiments which correspond to embodiments of the method of the invention (see further), Cbulk is then between 0.02wt% and 0.08wt%, or between 0.025wt% and 0.08wt, or between 0.025wt% and 0.06wt% or between 0.025wt% and 0.05wt%.
Curve 13 illustrates the case where decarburization has continued until the middle plane of the sheet. In this case, Cbulk is smaller than the initial C-level of the method, and the C-profile extends over each half-width of the sheet.
[0025] The decarburized sheet according to the invention further comprises Al, Mn and possibly S, Cu and Ca. Contrary to the prior art references, the oxygen level is to be kept lower than 0.01wt%. According to a preferred embodiment of the steel sheet of the invention, oxygen is not added deliberately to the composition, but is allowed only at impurity levels.
Fish scaling resistance is ensured by the higher initial C-level, so no oxide formation is required for this purpose. This means that no special alloying elements such as V are included. Also, N
is kept as low as possible.
Fish scaling resistance is ensured by the higher initial C-level, so no oxide formation is required for this purpose. This means that no special alloying elements such as V are included. Also, N
is kept as low as possible.
[0026] The Al-level in the sheet of the invention is between 0.012wt% and 0.07wt%, which is higher than the allowed Al-level in the prior art references cited above.
In the cited prior art documents Al needs to be limited to avoid deoxidation, so as to ensure the formation of the oxides that will work against fish-scaling. In the method of the invention (see further), Al is mandatory for deoxidation and binding of free N to avoid the ageing of the mechanical properties. When the Al-level is lower than 0.012wt%, insufficient deoxidation takes place, and binding of N is required through other means. Adding Al at levels higher than 0.07wt% means an increase in cost of the process, and a deterioration of the enamelling quality. A
more preferred range for the Al-level, related to more optimized conditions in terms of deoxidation and cost/enamelling quality is between 0.02wt% and 0.06wt%.
In the cited prior art documents Al needs to be limited to avoid deoxidation, so as to ensure the formation of the oxides that will work against fish-scaling. In the method of the invention (see further), Al is mandatory for deoxidation and binding of free N to avoid the ageing of the mechanical properties. When the Al-level is lower than 0.012wt%, insufficient deoxidation takes place, and binding of N is required through other means. Adding Al at levels higher than 0.07wt% means an increase in cost of the process, and a deterioration of the enamelling quality. A
more preferred range for the Al-level, related to more optimized conditions in terms of deoxidation and cost/enamelling quality is between 0.02wt% and 0.06wt%.
[0027] Mn is present between 0.12wt% and 0.45wt%.
This element is added to control the strength properties of the steel and to avoid the formation of free sulphur.
This element is added to control the strength properties of the steel and to avoid the formation of free sulphur.
[0028]
Copper, Sulphur and Calcium may optionally be added above the impurity level, more precisely in the ranges 0.025wt% to 0.1wt%, 0.008wt% to 0.04wt% and 0.0005wt% to 0.005wt% respectively. These elements improve the enamelling quality.
Copper, Sulphur and Calcium may optionally be added above the impurity level, more precisely in the ranges 0.025wt% to 0.1wt%, 0.008wt% to 0.04wt% and 0.0005wt% to 0.005wt% respectively. These elements improve the enamelling quality.
[0029] The balance of the composition of the steel sheet according to the invention consists of Fe and incidental impurities. The following elements may be present as impurities at levels which are preferably lower than the values (in wt%) given in table 1 :
Si < 0.1 P < 0.03 Ti < 0.01 Cr <0.2 Ni <0.2 As < 0.02 Sn < 0.02 Nb < 0.01 / <0.01 Sb < 0.02 Mo < 0.03 B < 0.0005 N < 0.007 Table 1 : impurity levels
Si < 0.1 P < 0.03 Ti < 0.01 Cr <0.2 Ni <0.2 As < 0.02 Sn < 0.02 Nb < 0.01 / <0.01 Sb < 0.02 Mo < 0.03 B < 0.0005 N < 0.007 Table 1 : impurity levels
[0030] In a steel sheet of the invention, the depth of the C-profile, being defined as the depth where the C-level reaches (Cmmi_k + Csurface) /2, is higher than 75 m, to ensure good enamelling capability.
According to an embodiment, said depth is between 130 m and 200 m.
According to an embodiment, said depth is between 130 m and 200 m.
[0031]
Steel sheets according to the invention, i.e. with a C-level at the surface between 0 and 0.015wt%
are suitable for 2C/1F enamelling, i.e. enamelling by applying a ground coat enamel, followed by an outer enamel coating, both coatings being subjected to one firing step, and for 1C/1F enamelling, i.e. enamelling by applying one enamel layer subjected to one firing step. Steel sheets with low C-levels (i.e. 0.005wt% and less) at the surface may be suitable also for Direct White Enamelling (DWE).
Steel sheets according to the invention, i.e. with a C-level at the surface between 0 and 0.015wt%
are suitable for 2C/1F enamelling, i.e. enamelling by applying a ground coat enamel, followed by an outer enamel coating, both coatings being subjected to one firing step, and for 1C/1F enamelling, i.e. enamelling by applying one enamel layer subjected to one firing step. Steel sheets with low C-levels (i.e. 0.005wt% and less) at the surface may be suitable also for Direct White Enamelling (DWE).
[0032]
According to a preferred embodiment, the rm value of a steel sheet according to the invention is between 1.8 and 2.1. This means that the steel sheet has better formability than the prior art steel sheets referred to above. In the present description, the 'rf value refers to the plastic strain ratio (also known as the anisotropy factor), being the ratio of the true strain in the width direction to the true strain in the thickness direction when a sheet material is pulled in uniaxial tension beyond its elastic limit. The 'rmf value is defined as 14(r90 + 2*r45 + ro), with r90, r.45 and ro the r-values as defined above, measured on samples oriented respectively at 90 , 45 and 0 with respect to the rolling direction. In a steel sheet according to the invention, fish scaling resistance is ensured by the higher initial C-level applied in the method (see further).
According to a preferred embodiment, the rm value of a steel sheet according to the invention is between 1.8 and 2.1. This means that the steel sheet has better formability than the prior art steel sheets referred to above. In the present description, the 'rf value refers to the plastic strain ratio (also known as the anisotropy factor), being the ratio of the true strain in the width direction to the true strain in the thickness direction when a sheet material is pulled in uniaxial tension beyond its elastic limit. The 'rmf value is defined as 14(r90 + 2*r45 + ro), with r90, r.45 and ro the r-values as defined above, measured on samples oriented respectively at 90 , 45 and 0 with respect to the rolling direction. In a steel sheet according to the invention, fish scaling resistance is ensured by the higher initial C-level applied in the method (see further).
[0033] The steel sheet of the invention can be produced by subjecting a steel slab with a specific initial steel composition to hot rolling, coiling and cold rolling, and by subjecting the cold-rolled sheet to continuous superficial decarburization. The initial composition is mainly characterized by a higher C-level compared to the prior art, and by a higher Al-level and a lower oxygen level. No deliberate addition of elements like V, Nb or B
is done, while still allowing to produce enamelled steel 5 sheets with a high fish scale resistance and good enamel surface quality. The initial C-level is between 0.02wt%
and 0.08wt%, more preferably between 0.025wt% and 0.08wt%.
This is higher than the initial C-levels disclosed in the prior art references referred to above.
Despite such 10 higher initial C-levels, the method of the invention allows to obtain steel sheets with improved formability characteristics compared to the prior art.
Whereas JP6116634 indicates that above 0.015wt% of initial carbon, it is not possible to obtain acceptable decarburization and good formability, the starting composition of the invention does not encounter these problems.
Decarburization is possible down to an acceptable level, while formability is excellent. When the initial C-level is lower than 0.02wt%, insufficient cementite formation occurs which deteriorates fish scale resistance. C-levels above 0.08wt% lead to too high strength levels and thus reduced formability.
Specific ranges for the initial C-level, related to more optimized characteristics in terms of fish scale resistance and strength/formability are between 0.025wt% and 0.06wt%
and between 0.025wt% and 0.05wt%.
is done, while still allowing to produce enamelled steel 5 sheets with a high fish scale resistance and good enamel surface quality. The initial C-level is between 0.02wt%
and 0.08wt%, more preferably between 0.025wt% and 0.08wt%.
This is higher than the initial C-levels disclosed in the prior art references referred to above.
Despite such 10 higher initial C-levels, the method of the invention allows to obtain steel sheets with improved formability characteristics compared to the prior art.
Whereas JP6116634 indicates that above 0.015wt% of initial carbon, it is not possible to obtain acceptable decarburization and good formability, the starting composition of the invention does not encounter these problems.
Decarburization is possible down to an acceptable level, while formability is excellent. When the initial C-level is lower than 0.02wt%, insufficient cementite formation occurs which deteriorates fish scale resistance. C-levels above 0.08wt% lead to too high strength levels and thus reduced formability.
Specific ranges for the initial C-level, related to more optimized characteristics in terms of fish scale resistance and strength/formability are between 0.025wt% and 0.06wt%
and between 0.025wt% and 0.05wt%.
[0034] The initial steel composition according to the method of the invention further comprises Al, Mn and possibly 0, S, Cu and Ca in the same ranges as the decarburized sheet described above, the balance being Fe and the incidental impurities listed in Table 1. A more preferred range for the initial Al-level, related to more optimized conditions in terms of deoxidation and cost/enamelling quality is between 0.02wt% and 0.06wt%.
According to a preferred embodiment of the method of the invention, oxygen is not added deliberately to the composition, but is allowed only at impurity levels.
According to a preferred embodiment of the method of the invention, oxygen is not added deliberately to the composition, but is allowed only at impurity levels.
[0035] The method of the invention comprises standard steps of hot rolling and cold rolling a steel slab of the above composition. According to the preferred embodiment, the slab is (re)heated at a temperature above 1050 C, subjected to hot rolling with a finishing temperature between 850 C and 950 C, and coiling at coiling temperature between 620 C and 770 C.
Still according to the preferred embodiment, cold rolling is performed with a reduction of minimum 50%. The final thickness of the cold rolled sheet is preferably between 0.2 and 2mm.
Still according to the preferred embodiment, cold rolling is performed with a reduction of minimum 50%. The final thickness of the cold rolled sheet is preferably between 0.2 and 2mm.
[0036] The decarburization anneal is done in an annealing furnace for continuous annealing (i.e. annealing while the cold-rolled sheet moves through the furnace at a given speed, said speed determining the anneal time, i.e.
the time spent at the annealing temperature) as known in the art, possibly provided with a vapour injection device for applying a given annealing atmosphere.
the time spent at the annealing temperature) as known in the art, possibly provided with a vapour injection device for applying a given annealing atmosphere.
[0037] Figure 2 shows an example of a lay-out of an annealing furnace usable in the method of the invention, starting with heating phase 1 wherein the temperature rises to the annealing temperature. Phase 2 represents the actual annealing (soaking) phase. Phase 3 is an overageing step. Phase 2 can consist of one or more periods with a different (constant or average) annealing temperature and a different annealing atmosphere in each period. Practically speaking, the different periods at different conditions can be obtained by dividing the annealing zone in subsections and by injecting H20 vapour into an atmosphere comprising H2, at various points along the annealing line (see example further in this description).
[0038]
According to the invention, the superficial decarburization is done under a decarburizing atmosphere comprising water vapour and hydrogen gas, the remainder being essentially nitrogen gas, with the H2 content between 1vol% and 95vo1%, the H20 content between 0.04vol% and 33vo1%, the ratio of partial pressures pH20/pH2 being between 0.04 and 0.5, more preferably between 0.04 and 0.25. The above composition describes the atmosphere at the start of the decarburizing time. It is clear that during decarburization, the atmosphere composition will change, primarily due to the decarburization reaction taking place (formation of H2 and CO). Also at the start of the decarburizing time, small amounts of other gases may already have formed or may be present as impurities in the atmosphere. The total pressure under which the superficial decarburization anneal takes place may be atmospheric pressure, or a pressure different from atmospheric but within generally known boundaries applied in this type of annealing process.
According to the invention, the superficial decarburization is done under a decarburizing atmosphere comprising water vapour and hydrogen gas, the remainder being essentially nitrogen gas, with the H2 content between 1vol% and 95vo1%, the H20 content between 0.04vol% and 33vo1%, the ratio of partial pressures pH20/pH2 being between 0.04 and 0.5, more preferably between 0.04 and 0.25. The above composition describes the atmosphere at the start of the decarburizing time. It is clear that during decarburization, the atmosphere composition will change, primarily due to the decarburization reaction taking place (formation of H2 and CO). Also at the start of the decarburizing time, small amounts of other gases may already have formed or may be present as impurities in the atmosphere. The total pressure under which the superficial decarburization anneal takes place may be atmospheric pressure, or a pressure different from atmospheric but within generally known boundaries applied in this type of annealing process.
[0039]
According to one embodiment, the decarburizing atmosphere can be prepared with a mixture of H2 and N2 with between 1,5 and 5% H2 in which H20 vapour is injected so that pH20/pH2 is between 0.04 and 0.5. The minimum value of this ratio ensures that sufficient H20 is present to obtain decarburization according to the formula C + H20 ' CO + H2. The maximum of said range ensures that oxidation of Fe and of the furnace is avoided. A more preferred range for pH20/pH2, related to more optimized conditions in terms of sufficient decarburization and avoiding the occurrence of Fe-oxidation is between 0.04 and 0.25.
According to one embodiment, the decarburizing atmosphere can be prepared with a mixture of H2 and N2 with between 1,5 and 5% H2 in which H20 vapour is injected so that pH20/pH2 is between 0.04 and 0.5. The minimum value of this ratio ensures that sufficient H20 is present to obtain decarburization according to the formula C + H20 ' CO + H2. The maximum of said range ensures that oxidation of Fe and of the furnace is avoided. A more preferred range for pH20/pH2, related to more optimized conditions in terms of sufficient decarburization and avoiding the occurrence of Fe-oxidation is between 0.04 and 0.25.
[0040] In the method of the invention, the decarburizing atmosphere is applied during at least one of said periods with a different (constant or average) annealing temperature and a different annealing atmosphere in each period, preferably during the totality of phase 2.
In the following, the 'decarburizing time' refers to the time spent under the conditions of the decarburizing atmosphere.
In the following, the 'decarburizing time' refers to the time spent under the conditions of the decarburizing atmosphere.
[0041] The decarburizing time and the anneal temperature are chosen so as to obtain a steel sheet according to the invention. It is within the skilled person's knowledge to find suitable combinations of decarburizing time and anneal temperature based on the examples given further in this description. According to a preferred embodiment, the decarburizing time is between 45s and 300s and the anneal temperature between 760 C and 850 C. When the ratio pH20/pH2 is lower than about 0.1, the decarburizing time is preferably higher than 70s. A
more preferred range of the anneal temperature, applicable in combination with any decarburizing time between 45s and 300s is between 800 C and 850 C. The temperature is not necessarily constant during the decarburizing time.
Fluctuations of the temperature may occur due to variations in the line speed for example. An over-ageing step may be applied at a temperature between 350 C and 450 C during a timespan between 100s and 500s. A skinpass may further be applied with a reduction of between 0.3% and 1.5%.
Examples
more preferred range of the anneal temperature, applicable in combination with any decarburizing time between 45s and 300s is between 800 C and 850 C. The temperature is not necessarily constant during the decarburizing time.
Fluctuations of the temperature may occur due to variations in the line speed for example. An over-ageing step may be applied at a temperature between 350 C and 450 C during a timespan between 100s and 500s. A skinpass may further be applied with a reduction of between 0.3% and 1.5%.
Examples
[0042]
Results from industrial trials performed by the applicant will be described hereafter, as well as a number of laboratory trials. All tested samples were produced from starting compositions according to the invention. The coiling temperature was 725 C. Two industrial trials were conducted. The thickness of the cold rolled sheet subjected to decarburization annealing in industrial trial 1 was 0.6mm; in the second industrial trial the thickness was lmm.
Results from industrial trials performed by the applicant will be described hereafter, as well as a number of laboratory trials. All tested samples were produced from starting compositions according to the invention. The coiling temperature was 725 C. Two industrial trials were conducted. The thickness of the cold rolled sheet subjected to decarburization annealing in industrial trial 1 was 0.6mm; in the second industrial trial the thickness was lmm.
[0043] The continuous annealing line in which the industrial trials were conducted consists of a heating section, two soaking areas, a cooling and an overaging part. The annealing atmosphere consisted mainly of a mixture of H2 and N2 , with H20 vapour being injected in the first and/or the second soaking area. In the first trial, H20 vapour was injected only in the second soaking area.
In the second trial, H20 was injected in the first and the second soaking area.
Overageing was performed in both trials at 400 C. The overageing time depended on the line speed, e.g. at 180m/min line speed, the overageing time was 232s.
Table 2 shows the annealing conditions for both trials (numbered trial 1 and trial 2).
Table 3 shows the composition besides C, for a number of the samples shown in table 1.
In the second trial, H20 was injected in the first and the second soaking area.
Overageing was performed in both trials at 400 C. The overageing time depended on the line speed, e.g. at 180m/min line speed, the overageing time was 232s.
Table 2 shows the annealing conditions for both trials (numbered trial 1 and trial 2).
Table 3 shows the composition besides C, for a number of the samples shown in table 1.
[0044] In industrial trial 1, the pH20/pH2 ratio is below the range of 0.04-0.5 in the first soaking area (due to the fact that no H20 injection is done). The decarburizing time in this trial is the time spent in the second soaking area, where the pH20/pH2 is within said range. This is an example therefore of a process wherein phase 2 as shown in figure 1 comprises a first period wherein the conditions of the present invention are not met, and a second period wherein these conditions are met.
Such a process falls within the scope of the present invention.
Such a process falls within the scope of the present invention.
[0045] In industrial trial 2, H20-injection was performed in both soaking areas. The decarburizing time indicated here is the time spent in soaking areas 1 and 2.
The anneal temperature is the average of the temperatures in soaking areas 1 and 2. The pH20/pH2 values indicated in table 1 are the average values in soaking area 1 in which more H20 was injected.
However, the pH20/pH2 in soaking area 2 is estimated to be also within the range of 0.04-0.5. In industrial trial 2, longer decarburizing times could be achieved as compared to the first trial, for similar line velocities, leading to stronger decarburization.
5 [0046] The laboratory trials (marked 'trial 3' in table 2), were conducted on samples which were subjected to a simulation of the continuous annealing step, at the conditions shown in table 2. These trials were conducted in an atmosphere of HNx with 5% H2, with H20 added to obtain 10 pH20/pH2 in the range [0.04-0.5].
[0047]
Samples from all three trials were subjected to an enamelling process wherein a ground coat enamel is deposited, this enamel being designed especially to determine the role of C in the enamel characteristics. It 15 was found that the adhesion of the enamelling layer was good for all tested samples. The enamelling aspect was good for C-levels at the surface of maximum 0.015wt%, and for profile depths of 75 m up to 250 m, as shown in table 1. There is no reason to conclude from the results however that the enamelling quality deteriorates at higher depth values than 250 m. Such higher depth values are therefore not excluded from the scope of the invention. All tested samples showed a good fish scale resistance.
[0048]
Table 2 summarizes the results after decarburization in terms of the C-level at the surface (i.e. minimum level of the C-profile, measured by GD-OES), the depth of the C-profile, and the quality of an enamel layer produced on the surface of the samples. Samples 25 to 35 yielded a bad enamelling aspect, which can be ascribed to either an insufficient depth of the C-profile (as determined by the depth where the C-level reaches (Csurface+Cbuld 2), and/or a C level at the surface which is too high. The reason for these negative results can be ascribed to the test conditions, either the anneal temperature which is too low, the decarburizing time too short, or the pH20/pH2 ratio too low, or a combination of these factors.
[0049] Table 4 shows the mechanical properties of a number of samples taken from the sheets of the industrial trials 1 and 2.
Importantly, the formability in terms of the rm value is excellent, despite the initial C-level which is higher than in the prior art : rm is between 1.8 and 2.1. These results prove that the method of the invention allows to produce steel sheets suitable for enamelling, starting from an initial C-level higher than 0.02wt%, the resulting sheets allowing good enamelling quality and fish scale resistance, and having very good formability characteristics.
decarb initial urizing anneal Acc. to Sam- Trial C time temp. 020/ C_surf depth enameling invention pie N nr (ppm) (s) ( C) 012 (-) (ppm) (pm) aspect ?
1 1 362 45 807 0,12 126 90 good Y
2 3 330 70 770 0,05 123 92 good Y
3 3 330 70 770 0,12 108 100 good Y
4 3 330 70 770 0,24 47 94* good Y
1 367 90 782 0,16 132 123 good Y
6 1 367 90 785 0,16 133 130 good Y
7 2 330 90 810 0,13 87 130* good Y
8 2 346 90 817 0,09 89 116* good Y
9 2 386 105 801 0,12 106 130 good Y
2 348 105 809 0,11 88 145* good Y
11 2 316 105 817 0,12 78 180 good Y
12 2 346 105 824 0,09 81 142* good Y
13 2 360 126 799 0,09 106 138* good Y
14 2 348 126 814 0,09 78 124* good Y
2 375 126 824 0,09 76 140* good Y
16 3 330 155 840 0,05 51 94* good Y
17 3 330 155 840 0,12 61 94* good Y
18 3 330 155 840 0,24 35 94* good Y
19 2 391 209 815 0,08 68 121* good Y
2 437 209 817 0,08 70 145* good Y
21 2 340 209 821 0,07 71 222 good Y
22 1 500 45 795 0,08 211 40 bad n 23 1 491 45 796 0,09 164 75 bad n 24 1 490 45 800 0,09 177 49 bad n 1 360 45 793 0,09 150 70 bad n 26 1 360 45 794 0,09 167 75 bad n 27 1 360 45 795 0,09 176 68 bad n 28 3 330 70 770 0,01 198 57 bad n 29 2 363 105 743 0,17 187 135 bad n 2 370 105 752 0,16 165 120 bad n 31 3 330 155 840 0,01 192 89 bad n Table 2 : Overview of experimental conditions and results 1 : lwt% = 104 ppm The depth-values given in table 1 are values of the depth where the C-level reaches (Csurface+Cblalk) /2 . The depth 5 measurements indicated with "F show the maximum depth which could be measured with the applied equipment. The real value is thus higher than this value.
Sample n Al(wt%) Mn(wt%) Cu (wt%) S (wt%) 1 0.024 0.18 0.022 0.0049 0.03 0.18 0.028 0.0046 6 0.028 0.19 0.041 0.0052 9 0.035 0.18 0.029 0.0088 11 0.034 0.17 0.028 0.0077 Table 3 : composition of samples (C-level in table 1, remaining elements are beneath impurity level, the remainder is Fe) initial Anneal Anneal sample C-level Temp time pH20/pH2 Rp0.2 Rm Thickness no (ppm) ( C) (s) (-) (MPa) (MPa) r_m (mm) 23 490 796 209 0,09 189 318 1,8 0,6 1 362 807 126 0,12 182 318 1,9 0,6 5 367 782 105 0,16 189 319 1,8 0,6 19 391 821 105 0,08 185 320 1,8 1 375 824 45 0,09 187 331 2,0 1 11 316 817 45 0,12 188 329 1,8 1 9 386 801 90 0,12 183 319 1,9 1 5 Table 4 : mechanical properties
The anneal temperature is the average of the temperatures in soaking areas 1 and 2. The pH20/pH2 values indicated in table 1 are the average values in soaking area 1 in which more H20 was injected.
However, the pH20/pH2 in soaking area 2 is estimated to be also within the range of 0.04-0.5. In industrial trial 2, longer decarburizing times could be achieved as compared to the first trial, for similar line velocities, leading to stronger decarburization.
5 [0046] The laboratory trials (marked 'trial 3' in table 2), were conducted on samples which were subjected to a simulation of the continuous annealing step, at the conditions shown in table 2. These trials were conducted in an atmosphere of HNx with 5% H2, with H20 added to obtain 10 pH20/pH2 in the range [0.04-0.5].
[0047]
Samples from all three trials were subjected to an enamelling process wherein a ground coat enamel is deposited, this enamel being designed especially to determine the role of C in the enamel characteristics. It 15 was found that the adhesion of the enamelling layer was good for all tested samples. The enamelling aspect was good for C-levels at the surface of maximum 0.015wt%, and for profile depths of 75 m up to 250 m, as shown in table 1. There is no reason to conclude from the results however that the enamelling quality deteriorates at higher depth values than 250 m. Such higher depth values are therefore not excluded from the scope of the invention. All tested samples showed a good fish scale resistance.
[0048]
Table 2 summarizes the results after decarburization in terms of the C-level at the surface (i.e. minimum level of the C-profile, measured by GD-OES), the depth of the C-profile, and the quality of an enamel layer produced on the surface of the samples. Samples 25 to 35 yielded a bad enamelling aspect, which can be ascribed to either an insufficient depth of the C-profile (as determined by the depth where the C-level reaches (Csurface+Cbuld 2), and/or a C level at the surface which is too high. The reason for these negative results can be ascribed to the test conditions, either the anneal temperature which is too low, the decarburizing time too short, or the pH20/pH2 ratio too low, or a combination of these factors.
[0049] Table 4 shows the mechanical properties of a number of samples taken from the sheets of the industrial trials 1 and 2.
Importantly, the formability in terms of the rm value is excellent, despite the initial C-level which is higher than in the prior art : rm is between 1.8 and 2.1. These results prove that the method of the invention allows to produce steel sheets suitable for enamelling, starting from an initial C-level higher than 0.02wt%, the resulting sheets allowing good enamelling quality and fish scale resistance, and having very good formability characteristics.
decarb initial urizing anneal Acc. to Sam- Trial C time temp. 020/ C_surf depth enameling invention pie N nr (ppm) (s) ( C) 012 (-) (ppm) (pm) aspect ?
1 1 362 45 807 0,12 126 90 good Y
2 3 330 70 770 0,05 123 92 good Y
3 3 330 70 770 0,12 108 100 good Y
4 3 330 70 770 0,24 47 94* good Y
1 367 90 782 0,16 132 123 good Y
6 1 367 90 785 0,16 133 130 good Y
7 2 330 90 810 0,13 87 130* good Y
8 2 346 90 817 0,09 89 116* good Y
9 2 386 105 801 0,12 106 130 good Y
2 348 105 809 0,11 88 145* good Y
11 2 316 105 817 0,12 78 180 good Y
12 2 346 105 824 0,09 81 142* good Y
13 2 360 126 799 0,09 106 138* good Y
14 2 348 126 814 0,09 78 124* good Y
2 375 126 824 0,09 76 140* good Y
16 3 330 155 840 0,05 51 94* good Y
17 3 330 155 840 0,12 61 94* good Y
18 3 330 155 840 0,24 35 94* good Y
19 2 391 209 815 0,08 68 121* good Y
2 437 209 817 0,08 70 145* good Y
21 2 340 209 821 0,07 71 222 good Y
22 1 500 45 795 0,08 211 40 bad n 23 1 491 45 796 0,09 164 75 bad n 24 1 490 45 800 0,09 177 49 bad n 1 360 45 793 0,09 150 70 bad n 26 1 360 45 794 0,09 167 75 bad n 27 1 360 45 795 0,09 176 68 bad n 28 3 330 70 770 0,01 198 57 bad n 29 2 363 105 743 0,17 187 135 bad n 2 370 105 752 0,16 165 120 bad n 31 3 330 155 840 0,01 192 89 bad n Table 2 : Overview of experimental conditions and results 1 : lwt% = 104 ppm The depth-values given in table 1 are values of the depth where the C-level reaches (Csurface+Cblalk) /2 . The depth 5 measurements indicated with "F show the maximum depth which could be measured with the applied equipment. The real value is thus higher than this value.
Sample n Al(wt%) Mn(wt%) Cu (wt%) S (wt%) 1 0.024 0.18 0.022 0.0049 0.03 0.18 0.028 0.0046 6 0.028 0.19 0.041 0.0052 9 0.035 0.18 0.029 0.0088 11 0.034 0.17 0.028 0.0077 Table 3 : composition of samples (C-level in table 1, remaining elements are beneath impurity level, the remainder is Fe) initial Anneal Anneal sample C-level Temp time pH20/pH2 Rp0.2 Rm Thickness no (ppm) ( C) (s) (-) (MPa) (MPa) r_m (mm) 23 490 796 209 0,09 189 318 1,8 0,6 1 362 807 126 0,12 182 318 1,9 0,6 5 367 782 105 0,16 189 319 1,8 0,6 19 391 821 105 0,08 185 320 1,8 1 375 824 45 0,09 187 331 2,0 1 11 316 817 45 0,12 188 329 1,8 1 9 386 801 90 0,12 183 319 1,9 1 5 Table 4 : mechanical properties
Claims (23)
1. A rolled steel sheet for enamelling, said sheet having a carbon profile, defined by a gradient in the C-level from a level C surface at at least one surface of the sheet, to a level C bulk in the bulk of the sheet, C bulk being higher than C surface and comprising:
C bulk higher than 0 and lower than or equal to 0.08wt%;
C surface between 0 and 0.015wt%;
Al between 0.012wt% and 0.07wt%;
Mn between 0.12wt% and 0.45wt%; and 0 lower than 0.01wt%, the balance being Fe and incidental impurities, and wherein the depth where the C-level reaches (C bulk+C surface)/2, is higher than 75µm.
C bulk higher than 0 and lower than or equal to 0.08wt%;
C surface between 0 and 0.015wt%;
Al between 0.012wt% and 0.07wt%;
Mn between 0.12wt% and 0.45wt%; and 0 lower than 0.01wt%, the balance being Fe and incidental impurities, and wherein the depth where the C-level reaches (C bulk+C surface)/2, is higher than 75µm.
2. The steel sheet according to claim 1, having an r m value between 1.8 and 2.1.
3. The steel sheet according to claim 1 or 2, wherein C surface is between 0.005wt% and 0.015wt%.
4. The steel sheet according to claim 1 or 2, wherein C surface is between 0 and 0.005wt%.
5. The steel sheet according to any one of claims 1 to 4, wherein C bulk is between 0.02wt% and 0.08wt%.
6. The steel sheet according to claim 5, wherein C bulk is between 0.025wt% and 0.08wt%.
7. The steel sheet according to claim 6, wherein C bulk is between 0.025wt% and 0.06wt%.
8. The steel sheet according to any one of claims 1 to 7, wherein the Al-level is between 0.02wt% and 0.06wt%.
9. The steel sheet according to any one of claims 1 to 8, wherein said depth is between 130µm and 200µm.
10. The steel sheet according to any one of claims 1 to 9, further comprising one or more of the following:
Cu between 0.025wt% and 0.1wt%;
S between 0.008wt% and 0.04wt%; and Ca between 0.0005wt% and 0.005wt%.
Cu between 0.025wt% and 0.1wt%;
S between 0.008wt% and 0.04wt%; and Ca between 0.0005wt% and 0.005wt%.
11. An enamelled steel sheet consisting of the steel sheet according to any one of claims 1 to 10, provided with an enamel layer.
12. A steel product produced from the sheet according to any one of claims 1 to 10.
13. An enamelled steel product consisting of the steel product according to claim 12, provided with an enamel layer.
14. A method for producing a rolled steel sheet for enamelling, comprising the steps of:
subjecting a steel slab to hot rolling followed by coiling, and cold rolling, so as to obtain a cold-rolled steel sheet, said slab comprising the following initial composition:
C between 0.02wt% and 0.08wt%;
Al between 0.012wt% and 0.07wt%;
Mn between 0.12wt% and 0.45wt%; and O lower than 0.01wt%, the balance being Fe and incidental impurities; and subjecting said cold-rolled sheet to a continuous annealing step, wherein said sheet is exposed during a decarburizing time to a decarburizing atmosphere comprising water vapour and hydrogen gas, wherein the H2 content is between 1vol% and 95vol%, the H2O content between 0.04vol% and 33vol%, the remainder being mainly nitrogen gas, the ratio pH2O/pH2 being between 0.04 and 0.5.
subjecting a steel slab to hot rolling followed by coiling, and cold rolling, so as to obtain a cold-rolled steel sheet, said slab comprising the following initial composition:
C between 0.02wt% and 0.08wt%;
Al between 0.012wt% and 0.07wt%;
Mn between 0.12wt% and 0.45wt%; and O lower than 0.01wt%, the balance being Fe and incidental impurities; and subjecting said cold-rolled sheet to a continuous annealing step, wherein said sheet is exposed during a decarburizing time to a decarburizing atmosphere comprising water vapour and hydrogen gas, wherein the H2 content is between 1vol% and 95vol%, the H2O content between 0.04vol% and 33vol%, the remainder being mainly nitrogen gas, the ratio pH2O/pH2 being between 0.04 and 0.5.
15. The method according to claim 14, wherein said continuous annealing takes place at an anneal temperature between 760 C and 850 C, and during a decarburizing time between 45s and 300s.
16. The method according to claim 15, wherein the anneal temperature is between 800 C and 850 C.
17. The method according to any one of claims 14 to 16, wherein the C-level is between 0.025wt% and 0.08wt%.
18. The method according to claim 17, wherein the C-level is between 0.025wt% and 0.06wt%.
19. The method according to any one of claims 14 to 18, wherein the Al-level is between 0.02wt% and 0.06wt%.
20. The method according to any one of claims 14 to 19, wherein the ratio pH2O/pH2 is between 0.04 and 0.25.
21. The method according to any one of claims 14 to 20, further comprising an over-ageing step at a temperature between 350 C and 450 C during a time span between 100s and 500s.
22. The method according to claim 21, further comprising a skinpass step with a reduction of between 0.3% and 1.5%.
23. The method according to any one of claims 14 to 22, wherein the slab further comprises one or more of the following:
Cu between 0.025wt% and 0.1wt%;
S between 0.008wt% and 0.04wt%; and Ca between 0.0005wt% and 0.005wt%.
Cu between 0.025wt% and 0.1wt%;
S between 0.008wt% and 0.04wt%; and Ca between 0.0005wt% and 0.005wt%.
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PCT/EP2011/055477 WO2012136270A1 (en) | 2011-04-08 | 2011-04-08 | A steel sheet suitable for enamelling and method for producing such a sheet |
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CA2832357A1 CA2832357A1 (en) | 2012-10-11 |
CA2832357C true CA2832357C (en) | 2016-06-07 |
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CA2832357A Active CA2832357C (en) | 2011-04-08 | 2011-04-08 | A steel sheet suitable for enamelling and method for producing such a sheet |
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US (3) | US20140065434A1 (en) |
EP (1) | EP2534271B1 (en) |
KR (1) | KR101645786B1 (en) |
CN (1) | CN103476955B (en) |
BR (1) | BR112013025885B1 (en) |
CA (1) | CA2832357C (en) |
DK (1) | DK2534271T3 (en) |
EA (1) | EA024029B1 (en) |
ES (1) | ES2545746T3 (en) |
HU (1) | HUE027485T2 (en) |
MX (1) | MX348721B (en) |
PL (1) | PL2534271T3 (en) |
PT (1) | PT2534271E (en) |
RS (1) | RS54209B1 (en) |
SI (1) | SI2534271T1 (en) |
UA (1) | UA111195C2 (en) |
WO (1) | WO2012136270A1 (en) |
ZA (1) | ZA201307344B (en) |
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US11236427B2 (en) | 2017-12-06 | 2022-02-01 | Polyvision Corporation | Systems and methods for in-line thermal flattening and enameling of steel sheets |
JP6806128B2 (en) * | 2018-01-09 | 2021-01-06 | Jfeスチール株式会社 | Judgment method of cold-rolled steel sheet and manufacturing method of cold-rolled steel sheet |
KR102305878B1 (en) * | 2019-12-20 | 2021-09-27 | 주식회사 포스코 | Steel sheet for enamel and method of manufacturing the same |
KR102405223B1 (en) * | 2020-11-05 | 2022-06-02 | 주식회사 포스코 | Steel sheet for enamel and method of manufacturing the same |
KR102469876B1 (en) * | 2020-12-18 | 2022-11-23 | 주식회사 포스코 | High strength cold-rolled enamel steel sheet with excellent adhesion, and method of manufacturing the same |
CN113913699A (en) * | 2021-10-26 | 2022-01-11 | 攀钢集团攀枝花钢铁研究院有限公司 | Production method of cold-rolled enamel steel with yield strength of 300MPa |
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US658A (en) * | 1838-03-26 | Machine fob pricking leatpier preparatory to stitching | ||
US3598658A (en) * | 1967-05-20 | 1971-08-10 | Yawata Iron & Steel Co | Method for manufacturing cold-rolled steel sheet |
EP0228242A3 (en) * | 1985-12-23 | 1989-03-22 | Tektronix, Inc. | Non-intrusive microprocessor performance analyzer |
JPH02282421A (en) | 1989-04-24 | 1990-11-20 | Nippon Steel Corp | Production of continuously cast and annealed non-aging steel sheet for enameling |
JPH06116634A (en) * | 1992-10-07 | 1994-04-26 | Nkk Corp | Production of steel sheet for porcelain enameling by continuous decarburizing annealing |
JPH06279864A (en) * | 1993-03-29 | 1994-10-04 | Sumitomo Metal Ind Ltd | Production of aluminum killed cold rolled steel sheet for porcelain enameling |
JP3067569B2 (en) * | 1995-01-25 | 2000-07-17 | 日本鋼管株式会社 | Enamelled steel with excellent nail skipping resistance, black spot resistance and aging resistance |
GB9614961D0 (en) | 1996-07-16 | 1996-09-04 | Perkin Elmer Ltd | Carrier and its use in the preparation of samples for spectroscopy |
KR100480201B1 (en) * | 2000-06-23 | 2005-04-06 | 니폰 스틸 코포레이션 | Steel sheet for porcelain enamel excellent in forming property, aging property and enameling characteristics and method for producing the same |
JP4954889B2 (en) * | 2005-11-09 | 2012-06-20 | 新日本製鐵株式会社 | Steel sheet for continuous casting enamel that is remarkably excellent in anti-tackiness and method for producing the same |
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2011
- 2011-04-08 MX MX2013011685A patent/MX348721B/en active IP Right Grant
- 2011-04-08 EP EP11713766.1A patent/EP2534271B1/en active Active
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- 2011-04-08 PL PL11713766T patent/PL2534271T3/en unknown
- 2011-04-08 PT PT117137661T patent/PT2534271E/en unknown
- 2011-04-08 KR KR1020137028187A patent/KR101645786B1/en active IP Right Grant
- 2011-04-08 EA EA201391455A patent/EA024029B1/en not_active IP Right Cessation
- 2011-04-08 CA CA2832357A patent/CA2832357C/en active Active
- 2011-04-08 DK DK11713766.1T patent/DK2534271T3/en active
- 2011-04-08 RS RS20150565A patent/RS54209B1/en unknown
- 2011-04-08 SI SI201130570T patent/SI2534271T1/en unknown
- 2011-04-08 CN CN201180069952.3A patent/CN103476955B/en active Active
- 2011-04-08 WO PCT/EP2011/055477 patent/WO2012136270A1/en active Application Filing
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- 2011-08-04 UA UAA201312956A patent/UA111195C2/en unknown
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2018
- 2018-12-21 US US16/230,485 patent/US20190112684A1/en not_active Abandoned
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Also Published As
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BR112013025885A2 (en) | 2016-12-20 |
CA2832357A1 (en) | 2012-10-11 |
ZA201307344B (en) | 2014-11-26 |
CN103476955A (en) | 2013-12-25 |
WO2012136270A1 (en) | 2012-10-11 |
EP2534271B1 (en) | 2015-06-03 |
MX2013011685A (en) | 2014-01-31 |
SI2534271T1 (en) | 2015-10-30 |
US20190112684A1 (en) | 2019-04-18 |
BR112013025885B1 (en) | 2022-05-24 |
HUE027485T2 (en) | 2016-09-28 |
PL2534271T3 (en) | 2015-10-30 |
EA201391455A1 (en) | 2014-11-28 |
ES2545746T3 (en) | 2015-09-15 |
US20140065434A1 (en) | 2014-03-06 |
EP2534271A1 (en) | 2012-12-19 |
EA024029B1 (en) | 2016-08-31 |
KR20140014248A (en) | 2014-02-05 |
MX348721B (en) | 2017-06-26 |
US20190112683A1 (en) | 2019-04-18 |
DK2534271T3 (en) | 2015-08-24 |
CN103476955B (en) | 2016-03-30 |
UA111195C2 (en) | 2016-04-11 |
KR101645786B1 (en) | 2016-08-04 |
PT2534271E (en) | 2015-10-09 |
RS54209B1 (en) | 2015-12-31 |
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