CN109477182A - High-strength steel sheet and its manufacturing method - Google Patents
High-strength steel sheet and its manufacturing method Download PDFInfo
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- CN109477182A CN109477182A CN201780046036.5A CN201780046036A CN109477182A CN 109477182 A CN109477182 A CN 109477182A CN 201780046036 A CN201780046036 A CN 201780046036A CN 109477182 A CN109477182 A CN 109477182A
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- 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
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- 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
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
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- 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
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/18—Hardening; Quenching with or without subsequent tempering
- C21D1/19—Hardening; Quenching with or without subsequent tempering by interrupted quenching
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- 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
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/005—Heat treatment of ferrous alloys containing Mn
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- 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
- C21D6/00—Heat treatment of ferrous alloys
- C21D6/008—Heat treatment of ferrous alloys containing Si
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- 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
- C21D9/48—Heat treatment, e.g. annealing, hardening, quenching or tempering, adapted for particular articles; Furnaces therefor for sheet metals deep-drawing sheets
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- 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
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- 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
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/02—Ferrous alloys, e.g. steel alloys containing silicon
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- 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
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- 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
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- Crystallography & Structural Chemistry (AREA)
- Heat Treatment Of Sheet Steel (AREA)
Abstract
A kind of high-strength steel sheet, wherein, contain the C:0.15 mass mass of %~0.35 %, Si's and Al is total: 0.5 mass of mass %~3.0 %, the Mn:1.0 mass mass of %~4.0 %, P:0.05 mass % or less, S:0.01 mass % or less, surplus is made of Fe and inevitable impurity, in structure of steel, ferrite divides rate to be 5% or less, tempered martensite and the total of tempering bainite divide rate to be 60% or more, remained austenite content is 10% or more, the average-size of MA is at 1.0 μm or less, half breadth with the concentration distribution of the Mn in the carbon thickening region of remained austenite content equivalent is 0.3 mass % or more, the q value of small angle X ray scattering is 1nm- 1Scattering strength in 1.0cm- 1Below.
Description
Technical field
This disclosure relates to can the high-strength steel sheet used in the various uses headed by auto parts.
Background technique
For the steel plate of automobile part etc., in order to realize lightweight and crashworthiness together, the raising of intensity is taken into account
With the raising of impact property.
Such as patent document 1 discloses a kind of high-strength steel sheet, by heating of plate blank to 1210 DEG C or more, controls hot rolling item
Part, so that 0.5 μm of fine TiN particle below be made to generate, inhibiting the partial size of the starting point as low temperature damage is 1 μm or more
Thus the generation of AlN particle attempts to improve impact property.
A kind of high-strength steel sheet is disclosed in patent document 2, and C amount is made to be higher than 0.45% and 0.77% hereinafter, making
Mn amount be 0.1% or more, 0.5% hereinafter, make Si amount be 0.5% hereinafter, and regulation Cr, Al, N, O additive amount, while making iron
50% or more of ferritic partial size becomes the mesh-shape tissue engaged with hard, to try hard to improve impact resistant characteristic.
A kind of high-strength steel sheet is disclosed in patent document 3, by the Mn of addition 3.5~10%, makes residual austenite
The amount of body is 10% or more, makes 1.5 μm of the equispaced of retained austenite hereinafter, to seek the improvement of impact resistant characteristic.
Patent document 4 discloses a kind of tensile strength with 980~1180MPa, and shows good deep drawability
High-strength steel sheet.
[existing technical literature]
[patent document]
No. 5240421 specifications of [patent document 1] Japanese Patent No.
[patent document 2] Japanese Unexamined Patent Publication 2015-105384 bulletin
[patent document 3] Japanese Unexamined Patent Publication 2012-251239 bulletin
[patent document 4] Japanese Unexamined Patent Publication 2009-203548 bulletin
In order to realize the further lightweight of steel plate used in automobile part, need it thinner, while being also equipped with and filling
The intensity and impact property divided.In short, requiring the steel plate of higher tensile strength and excellent impact characteristics.
In addition, not only requiring high-tensile in the various uses using automobile part as representative and impact being special
Property, but also there is excellent strength-ductility balanced, high-yield-ratio, the formability that swells and excellent hole expansibility.
It is specifically wanted respectively about tensile strength, strength-ductility balanced, yield tensile ratio, deep draw characteristics and hole expansibility
Ask as follows.
About tensile strength, it is desirable that in 980MPa or more.In order to improve the stress for capableing of load in use, in addition to high tensile
Other than intensity (TS), it is also necessary to have high-yield strength (YS).In addition, from the viewpoint of ensuring crashworthiness etc., it is also necessary to
The yield strength of steel plate is improved, in addition to showing strength characteristics stabilization in collision, it is also desirable to fracture when thering is inhibition to deform
Characteristic.Therefore, specifically, it is desirable that have 0.75 or more yield tensile ratio (YR=YS/TS), and as replacement destruction characteristic
Evaluation index, it is desirable that the plate thickness reduction of fracture when tension test improves.In addition, the basic nature as automotive sheet
Can, also require the strength of joint of spot-welding part.Specifically, it is desirable that the cross tensile strength of spot-welding part is 6kN or more.
About strength-ductility balanced, it is desirable that the product (TS × EL) of TS and breaking elongation (EL) be 20000MPa% with
On.In addition, formability when in order to ensure part forming, also requiring the hole expansibility λ for indicating hole expandability is 20% or more, Yi Jibiao
The limit bulging height (bulging height) for showing the formability that swells is 16mm or more.
But all meets these requirements in high-strength steel sheet and be difficult, so wanting disclosed in the Patent Documents 1 to 4
Seek a kind of high-strength steel sheet that can all meet these requirements.
Summary of the invention
Embodiments of the present invention as reply precisely in order to requiring and making, it is intended that providing a kind of anti-
It is disconnected when tensile strength (TS), yield tensile ratio (YR), product (TS × EL), the hole expansibility (λ), tension test of (TS) and breaking elongation (EL)
The cross tensile strength (stretching of SW cross) for splitting the plate thickness reduction (RA) in portion, limit bulging height and spot-welding part is in Gao Shui
Flat high-strength steel sheet and its manufacturing method.
Mode 1 of the invention is a kind of high-strength steel sheet, wherein contain
The C:0.15 mass mass of %~0.35 %,
Si's and Al is total: 0.5 mass of mass %~3.0 %,
The Mn:1.0 mass mass of %~4.0 %,
P:0.05 mass % or less,
S:0.01 mass % hereinafter,
Surplus is made of Fe and inevitable impurity,
In structure of steel,
Ferrite divide rate be 5% hereinafter,
Tempered martensite and the total of tempering bainite divide rate to be 60% or more,
Remained austenite content is 10% or more,
The average-size of MA be 1.0 μm hereinafter,
Half breadth with the concentration distribution of the Mn in carbon that remained austenite content is equivalent thickening region is 0.3 mass %
More than,
The q value of small angle X ray scattering is 1nm- 1Scattering strength in 1.0cm- 1Below.
Mode 2 of the invention, according to high-strength steel sheet described in mode 1, wherein C amount is 0.30 mass % or less.
Mode 3 of the invention, the high-strength steel sheet according to mode 1 or 2, wherein Al amount is lower than 0.10 mass %.
Mode 4 of the invention is a kind of manufacturing method of high-strength steel sheet, wherein comprise the following steps:
The process for preparing rolled stock, it is total containing the C:0.15 mass mass of %~0.35 %, Si and Al: 0.5 matter
Mass %, the Mn:1.0 mass of %~3.0 mass %, the P:0.05 mass of %~4.0 % or less, S:0.01 mass % are measured hereinafter, remaining
Amount is made of Fe and inevitable impurity;
By the rolled stock in Ac1Point and 0.2 × Ac1+ 0.8 × Ac of point3After being kept for 5 seconds or more at a temperature of between point, add
Heat is to Ac3Or more temperature and kept for 5~600 seconds and the process that carries out austenitizing;
After the austenitizing, with 10 DEG C/sec or more of average cooling rate, it is cooled to from 650 DEG C or more of temperature
100 DEG C more than or lower than 300 DEG C between the cooling process stopped until temperature;
With 30 DEG C/sec or more of average heating rate, it is heated to from the cooling stopping temperature in 300 DEG C~500
Process until the relation reheating temperature of DEG C range;
Under the relation reheating temperature, when being 10000~14500 and keep to meet the tempering parameter P as defined in formula (1)
Between the process that is kept for 1~300 second mode;With
After the holding, being cooled to 200 DEG C from the relation reheating temperature with 10 DEG C/sec or more of average cooling rate is
Process only.
P=T × (20+log (t/3600)) ... (1)
Here, T: temperature (K), t: time (second).
Mode 5 of the invention, according to manufacturing method described in mode 4, wherein cold until the cooling stopping temperature
But in, comprising: be cooled to the temperature as 650 DEG C or more using 0.1 DEG C/sec of average cooling rate more than or lower than 10 DEG C/sec
Chilling start temperature until process;It is cooled to from the chilling start temperature with 10 DEG C/sec of average cooling rate or more
Process until the cooling stopping temperature.
Mode 6 of the invention, the manufacturing method according to mode 4 or 5, wherein the tempering parameter be 11000~
14000, the retention time is 1~150 second.
Embodiment according to the present invention is capable of providing tensile strength (TS), yield tensile ratio (YR), (TS) and breaking elongation
(EL) the plate thickness reduction (RA) (impact property) of fracture when product (TS × EL), hole expansibility (λ), tension test, pole
Limit bulging height and the cross tensile strength (stretching of SW cross) of spot-welding part are in high-caliber high-strength steel sheet and its manufacture
Method.
Detailed description of the invention
Fig. 1 is the manufacturing method for illustrating the high-strength steel sheet of embodiments of the present invention, the diagram being especially heat-treated.
Specific embodiment
The present inventors' sharp study as a result, it has been found that, in the steel with defined ingredient, by making structure of steel (metal
Tissue) in, reach ferrite point rate: 5% hereinafter, tempered martensite and tempering bainite total point of rate: 60% or more, it is remaining
γ amount: the average-size of 10% or more, MA: 1.0 μm hereinafter, be equivalent in the part of retained austenite, i.e. carbon thickening region
The half breadth of the concentration distribution of Mn: 0.3 mass % or more, furthermore the q value of small angle X ray scattering is 1nm- 1Scattering strength:
1.0cm- 1Hereinafter, can then obtain tensile strength (TS), yield tensile ratio (YR), the product (TS × EL) of (TS) and breaking elongation (EL),
Plate thickness reduction (RA) (impact property), limit bulging height and the spot-welding part of fracture when hole expansibility (λ), tension test
Cross tensile strength (stretching of SW cross) be in high-caliber high-strength steel sheet.
Although details are aftermentioned, there is Mn to be thickened region, be to manufacture for the high-strength steel sheet of embodiments of the present invention
When heat treatment austenitizing process in, by Ac1Point and Ac3The two-phase coexisting region of the centre of point, in more detail,
It is exactly in Ac1Point~0.2 × Ac1+ 0.8 × Ac of point3After being kept for the stipulated time at a temperature of between point, then with Ac3Or more temperature
Degree is kept for the stipulated time and is formed.In addition, being also formed in heat treatment corresponding with retained austenite (with retained austenite
Amount is same amount of) carbon thickening region.Moreover, the carbon thickening region in, formed Mn thickening region and Mn be not thickened region this
The two.That is, existing among carbon thickening region (retained austenite) containing more Mn and really not so region.Therefore, if
It is thickened the distribution of region (that is, corresponding to whole retained austenites) measurement Mn concentration in entire carbon, then Mn concentration has certain journey
Degree or more deviation.Specifically, the half breadth of the concentration distribution of Mn is 0.3 mass % or more.
In this way, the Mn amount for containing retained austenite is fluctuated, it is meant that can have has the residual of various stability
Remaining austenite.Just cause to process the low retained austenite of stability of induced transformation and with large strain with lesser dependent variable
The retained austenite mixing that the stability for processing induced transformation is high can just be caused, can cause to add in various strain regions
Work induced transformation.As a result, high n-value can be proposed in wide strain region, it can be improved strain dispersibility and realize high swollen
Shape processability.
The high-strength steel sheet of embodiments of the present invention presented below and its details of manufacturing method.
1. structure of steel
Illustrate the details of the structure of steel of the high-strength steel sheet of embodiments of the present invention below.
In the explanation of structure of steel below, have for can be improved with such tissue the mechanism of various characteristics into
The case where row illustrates.These are the mechanism that the present inventors are expected based on the cognition obtained at present, it is noted that,
It is not to define the range of technology of the invention.
(1) ferrite divides rate: 5% or less
Ferrite is typically of problem, although excellent in workability, intensity is low.As a result, if ferrite content is more,
Then yield tensile ratio reduces.Therefore, make 5% or less ferrite point rate (5 volume % or less).
Ferrite point rate is preferably 3% hereinafter, more preferably 1% or less.
Ferrite point rate can be acquired by being observed with optical microscopy with the region of counting method measurement white.That is,
By such method, ferrite point rate can be acquired with area ratio (area %).It then, can be straight with the value that area ratio acquires
It connects and is used as the value of volume ratio (volume %).
(2) total rate of dividing of tempered martensite and tempering bainite: 60% or more
60% or more the total point of rate (60 volume % or more) for making tempered martensite and tempering bainite, can make high-strength
Degree is taken into account with high hole expandability.Total point of rate of tempered martensite and tempering bainite is preferably 70% or more.
Tempered martensite and tempering bainite amount (total to divide rate), can acquire, that is, in the following way for carrying out
The section progress SEM observation of nital corrosion, measurement MA (that is, the martensite of retained austenite and as-quenched
It is total) divide rate, above-mentioned ferrite point rate and MA points of rate are subtracted from whole structure of steel and is acquired.
(3) remained austenite content: 10% or more
Retained austenite is in the processing of punch process etc., it may occur that mutually becomes martensite due to processing induced transformation
TRIP phenomenon can obtain big elongation percentage.In addition, being formed by martensite with high rigidity.Therefore, it can obtain excellent
It is strength-ductility balanced.Make 10% or more remained austenite content (10 volume % or more), can be realized TS × EL is
Excellent in this way strength-ductility balanced of 20000MPa% or more.
Remained austenite content is preferably 15% or more.
In the high-strength steel sheet of embodiments of the present invention, the most of of retained austenite exists in the form of MA.It is so-called
MA is the abbreviation of martensite-austenite constituent, is the complex (complex group of martensite and austenite
It knits).
Remained austenite content can utilize X-ray diffraction, acquire ferrite (containing tempered martensite and not in X-ray diffraction
The martensite of tempering) with the diffracted intensity ratio of austenite, then by calculating acquirement.As x-ray source, it is able to use Co-K α
Ray.
(4) average-size of MA: 1.0 μm or less
MA is hard phase, and when deformation forms point as hole in parent phase/hard phase interface neighborhood and works.MA size is thicker
Greatly, it can more cause strain to be concentrated to parent phase/hard phase interface, be easy to happen to be formed in parent phase/hard phase interface neighborhood hole
For the destruction of starting point.
Therefore, making MA size, especially MA average-size is 1.0 μm or less fine in this way, inhibits to destroy, then can make to expand
Porosity λ is improved.
The average-size of MA is preferably 0.8 μm or less.
The average-size of MA can acquire in the following way, that is, for passing through the section of nital corrosion,
With SEM with 3000 times or more observations, 3 visuals field more than, total 200 μm or more of straight line is drawn in the arbitrary position in photo, survey
The slice length that the straight line intersects with MA is measured, the average value of the slice length is calculated.
(5) half breadth with the Mn concentration distribution in the carbon of remained austenite content equivalent thickening region is 0.3 mass %
More than
As above-mentioned, the most of of retained austenite exists in the form of MA, only identifies remnants using optical microscopy or SEM
Austenite is had any problem.Retained austenite is compared with ferrite etc., since the solid solution limit of carbon is big, so by carrying out at aftermentioned heat
Reason, and it is thickened carbon in retained austenite.Therefore, it using EPMA (Electron Probe Micro Analyzer), carries out
The element image of carbon, by acquired from the high measurement point of concentration of carbon sequentially through above-mentioned X-ray diffraction and retained austenite
The measurement point for measuring equivalent is thickened region as carbon, and it is retained austenite which can be thickened to region decision.That is, for example, remaining
When Ovshinsky scale of construction is 15 volume %, in the measurement point for measuring carbon amounts by element image, the side selection high from concentration of carbon
15%, and the measurement point (carbon thickening region) that these concentration of carbons are high may determine that as retained austenite.
Therefore " region is thickened with the carbon of remained austenite content equivalent ", it is meant that be equivalent to the (right therewith of retained austenite
Answer) region.
Then, about the concentration distribution with the Mn in the carbon of remained austenite content equivalent thickening region, especially Mn is dense
The half breadth for spending distribution is also able to use EPMA measurement.Make be considered as carbon thickening region measurement point Mn amount distribution
Graphically, hereby it is possible to obtaining half breadth.
The half breadth of the Mn concentration distribution is bigger, and the deviation of the Mn concentration in expression retained austenite is bigger, and (Mn's is dense
The range for spending distribution is wide).In the high-strength steel sheet of embodiments of the present invention, the half breadth of the concentration distribution of Mn is 0.3
Quality % or more, preferably 0.5 mass % or more, more preferably 0.6 mass % or more, further preferably 0.75 mass % with
On.
In this way, the Mn amount fluctuation for containing retained austenite (carbon thickening region), is capable of forming the remnants low from stability
The austenite retained austenite wide to the such stability range of the high retained austenite of stability.The low residual austenite of stability
Processing induced transformation just occurs under small dependent variable, becomes martensite for body.The high retained austenite of stability, will not be by small
Dependent variable cause to process induced transformation, only apply big dependent variable just and can cause and process induced transformation and become martensite.
Therefore, if the retained austenite with the wide stability of range exists, the processing by just and when small dependent variable, cross over
To when processing progress and big dependent variable, processing induced transformation can constantly occur.As a result, can be answered across roomy
Become range and propose high n-value, can be improved strain dispersibility and realize high bulging processability.
(6) the q value of small angle X ray scattering is 1nm- 1Scattering strength in 1.0cm- 1Below
So-called small angle X ray scattering is for steel plate X-ray irradiation, and measurement penetrates the scattering of the X-ray of steel plate, thus
The size distribution of minuteness particle contained in steel plate (for example, being dispersed in the cementite particle in steel plate) can be acquired.In this hair
In the steel plate of bright embodiment, by small angle X ray scattering, the conduct microfine being dispersed in tempered martensite can be acquired
The size distribution of the cementite particle of son.Specifically, it in small angle X ray scattering, with q value and scattering strength, can solve
It analyses the size of the particle of cementite and its divides rate.
Q value is the index of the size of the particle (such as cementite particle) in steel plate.It is so-called that " q value is 1nm- 1", correspond to
The cementite particle of partial size about 1nm.Scattering strength is the index of the volume fraction of the particle (such as cementite particle) in steel plate.
Scattering strength is stronger, indicates that the volume fraction of cementite is bigger.
About the scattering strength of a certain q value, the volume of the cementite particle of size corresponding to the q value is semi-quantitatively indicated
Divide rate.For example, q value is 1nm- 1Scattering strength, semi-quantitatively indicate the volume fraction of the fine cementite particle of about 1nm.
That is, q value is 1nm- 1Scattering strength it is big, indicate about 1nm fine cementite particle volume fraction it is big.?
" q value is 1nm- 1Scattering strength in 1.0cm- 1In steel plate below ", it is meant that about 1nm's is fine present in the steel plate
The volume fraction of cementite particle (is equivalent to scattering strength in 1.0cm in defined value- 1Value) below.As described below, " q
Value is 1nm- 1Scattering strength in 1.0cm- 1Steel plate below ", because the volume fraction of the cementite of about 1nm is suppressed low,
It is believed that impact resistant excellent.
In the high ductile steel containing remaining γ, the preferably carbon state that concentrates on retained austenite, it is generally desirable to not deposit
In cementite.The partial size dispersed in steel is the fine cementite of 1nm or so, can interfere moving for dislocation and make the changes of steel
Shape ability reduces.Therefore, in the steel more than the volume fraction of the cementite of partial size about 1nm, destruction when deformation is promoted, resistance to
Collision characteristic can reduce.
The steel plate of embodiments of the present invention, by inhibiting low the volume fraction of fine cementite, more specifically
It says, is to make q value 1nm- 1Scattering strength be in 1cm- 1Hereinafter, fine to make to be formed by the lath of tempered martensite
Carbide reduce, to improve the deformability in martensite.Inhibit steel plate to destroy in collision as a result, makes steel plate
Impact resistant characteristic improves.
The measurement of small angle X ray scattering is measured using RIGAKU society Nano-viewer, Mo pipe ball.From steel plate
The disc shaped test piece for cutting Φ 3mm is cut the sample of 20 μ m-thicks near plate thickness 1/4, is used as sample.Q value takes 0.1~
10nm- 1Data.It wherein, is 1nm for q value- 1And acquire absolute intensity.
(7) other structure of steel:
In the present specification, other than the ferrite, tempered martensite, tempering bainite, retained austenite and cementite
Structure of steel there is no special provision.But other than the structure of steel of these ferrites etc., there is also pearlite, it is not tempered
Bainite and the martensite not being tempered etc..The structure of steel of ferrite etc., if meeting organization condition above-mentioned, even if in steel
There are pearlite etc., can still play effect of the invention.
2. composition
It is illustrated below for the composition of the high-strength steel sheet of embodiments of the present invention.Mainly for basic element C,
Si, Al, Mn, P and S are illustrated.
In addition, being indicated at the % for being grouped as middle unit, the entirely meaning of quality %.
(1) C:0.15~0.35%
C increases the amount of expected tissue, especially remnants γ, be for ensuring that it is high-intensitive-ductility balanced (TS ×
EL balance) etc. characteristic necessary to element need to add 0.15% or more to effectively play such effect.But
It is unsuitable for welding higher than 0.35%.Preferably 0.18% or more, more preferably 0.20% or more.Additionally, it is preferred that being 0.30%
Below.If C amount 0.25% hereinafter, if can more easily be welded.
(2) Si's and Al is total: 0.5~3.0%
Si and Al inhibits the precipitation of cementite respectively, has the function of keeping retained austenite remaining.In order to effectively play
Such effect needs to add Si and Al total 0.5% or more.But if the total of Si and Al is higher than 3.0%, the change of steel
Shape ability reduces, and TS × EL and bulging height reduce.Preferably 0.7% or more, more preferably 1.0% or more.Additionally, it is preferred that being
2.5% or less.
In addition, can be the additive amount of this degree to work as deoxidant element about Al, 0.10 matter can be lower than
% is measured, in addition, making increased purpose of remained austenite content etc. for the formation for for example inhibiting cementite, 0.7 matter can also be added
Measure % or more amounts more in this way.
(3) Mn:1.0~4.0%
Mn inhibits ferritic formation.In addition, Mn, which forms Mn, is thickened region, the different retained austenite of stability is formed,
It is that bulging processability is made to improve the indispensable element of institute.In order to effectively play such effect, need to add 1.0% with
On.But if being higher than 4.0%, the temperature range of two phase regions heating is uncontrollable that narrow and temperature becomes too low, because
This, even if with Ac1Point~0.2 × Ac1+ 0.8 × Ac of point3Temperature between point is kept for the stipulated time, and phase transformation will not be carried out, be deposited
The case where cannot form the thickening region Mn.Preferably 1.5% or more, more preferably 2.0% or more.Additionally, it is preferred that being 3.5%
Below.
(4) P:0.05% or less
P is inevitably present as impurity element.If being deteriorated with the presence of P, EL and the λ higher than 0.05%.Therefore, P
Content be 0.05% or less (contain 0%).Preferably 0.03% or less (containing 0%).
(5) S:0.01% or less
S is inevitably present as impurity element.If the S higher than 0.01% exists, the sulfide-based of MnS etc. is formed
Field trash becomes the starting point of crackle and reduces λ.Therefore, the content of S was 0.01% or less (containing 0%).Preferably 0.005%
(contain 0%) below.
(6) surplus
In a preferred embodiment, surplus is iron and inevitable impurity.As inevitable impurity, permit
Perhaps microelement (for example, As, Sb, the Sn's etc.) brought by the situation of raw material, goods and materials, manufacturing equipment etc. is mixed into.In addition, example
Such as, as P and S in this way, in general, the content the few the more preferred, therefore it is inevitable impurity, but in this compositing range, had
The element made separate stipulations as so above-mentioned.Therefore, in the present specification, " inevitable impurity " this feelings of surplus are constituted
Condition is the concept removed other than the element that its compositing range is made separate stipulations.
But it is not limited by this embodiment.As long as being able to maintain that the spy of the high-strength steel sheet of embodiments of the present invention
Property, it can further contain arbitrary other elements.
3. characteristic
Such as the high-strength steel sheet of above-mentioned embodiments of the present invention, TS, YR, TS × EL, λ, impact resistant characteristic, limit bulging
Height and the stretching of SW cross are in high level.Hereinafter, these characteristics of the high-strength steel sheet for embodiments of the present invention
It is described in detail.
(1) tensile strength (TS)
TS with 980MPa or more.It is preferred that TS is 1180MPa or more.This is because, if TS is lower than 980MPa, although
Receiving load when can more reliably obtain excellent fracture characteristics, but collide is lower, therefore is not preferred.
(2) yield tensile ratio (YR)
With 0.75 or more yield tensile ratio.Realize that high yield is strong thus, it is possible to combine with above-mentioned high-tensile
Degree, the final product as obtained from the processing of deep-draw processing etc. can use under high stress.It is preferred that with 0.80 or more
Yield tensile ratio.
(3) product (TS × EL) of TS and breaking elongation (EL)
TS × EL is 20000MPa% or more.TS × EL with 20000MPa% or more can be had height simultaneously
Intensity and high ductibility it is high-caliber strength-ductility balanced.It is preferred that TS × EL is 23000MPa% or more.
(4) formability that swells (limit bulging height)
Limit bulging height is the index for the evaluation for the formability that swells.Limit bulging height, in load-stroke line
In figure for load sharply reduction fracture occur when punching stroke.
In more detail, with the test film of Φ 120mm, with Φ 53.6mm, the bulb of the punch die of shoulder radius 8mm and Φ 50mm
Formed punch, presss from both sides the polythene strip every lubrication between formed punch and steel plate, and pressure-pad-force carries out bulging, measurement fracture as 1000kgf
When height (punching stroke), acquire limit bulging height.
The high-strength steel sheet of embodiments of the present invention, limit bulging height are 20mm or more, preferably 21mm or more.
(5) hole expansibility (λ)
Hole expansibility λ follows Nippon Steel alliance specification JFS T1001 and acquires.Diameter d is dug on test film0(d0=10mm)
Perforation, be that 60 ° of formed punch is pressed into the perforation by toe angle, measure generation cracking penetrated through test film plate thickness this
The diameter d of the perforation at moment, acquires hole expansibility according to the following formula.
λ (%)={ (d-d0)/d0}×100
The high-strength steel sheet of embodiments of the present invention, hole expansibility λ are 20% or more, preferably 30% or more.Thus, it is possible to
Access the excellent processability such as press formability.
(6) the plate thickness reduction in tension test (R5 stretches plate thickness reduction)
Using the test film for the arc-shaped notch for being equipped with radius 5mm on No. 5 test films, make the deformation speed of tension test
Degree is tested for 10mm/min, is broken sample.Thereafter, cross-section observation is carried out, with the thickness t in the plate thickness direction in section1
Divided by the plate thickness t of script0Value (t1/t0), as plate thickness reduction.
Plate thickness reduction in the test is 50% or more, preferably 52% or more, more preferably 55% or more.As a result,
It is difficult to be broken severely deformed when collision, therefore the steel plate for the impact property for having excellent can be obtained.
(7) the cross tensile strength of spot welding
The cross tensile strength of spot welding is evaluated in accordance with JIS Z 3137.The condition of spot welding is used two
The steel plate of 1.4mm is overlapped.With dome radius (ド ー system ラ ジ ア ス) electrode of type makes electric current from 6kA at plus-pressure 4kN
Range to 12kA increases 0.5kA every time and carries out spot welding, the current value (minimum current for (Chi り) generation of splashing when investigation is welded
Value).Spot welding is carried out with electric current 0.5kA lower than the minimum current value, is drawn the cruciform joint being thus welded as cross
Stretch the measuring sample of intensity.The above are " good " in 6kN for cross tensile strength.In addition, cross tensile strength is preferably 8kN
More than, more preferably 10kN or more.
If cross tensile strength is 6kN or more, when manufacturing automobile part etc. by steel plate, when can obtain welding
The high part of bond strength.
4. manufacturing method
Next, being illustrated for the manufacturing method of the high-strength steel sheet of embodiments of the present invention.
Present inventors found that (more by carrying out the aftermentioned heat treatment of details for the rolled stock with defined composition
The means of isothermal quenching of grade), to have above-mentioned desired structure of steel, as a result, can obtain that there are above-mentioned expected characteristics
High-strength steel sheet.
Illustrate its details below.
Fig. 1 is the manufacturing method for illustrating the high-strength steel sheet of embodiments of the present invention, the diagram being especially heat-treated.
Implement the rolled stock of heat treatment, usually after hot rolling, carries out cold rolling and manufacture.But it's not limited to that, carries out
Any one of hot rolling and cold rolling can manufacture.In addition, the condition of hot rolling and cold rolling is not particularly limited.
(1) austenitizing
In austenitizing process, as shown in [2] of Fig. 1, by rolled stock in Ac1Point and Ac3The two-phase coexistence of the centre of point
Domain is exactly in more detail in Ac1Point and 0.2 × Ac1+ 0.8 × Ac of point3Temperature T between point1(Ac1≤T1≤0.2×Ac1
+ 0.8 × Ac of point3) under kept for 5 seconds or more after, as shown in [3] of Fig. 1, [4], then end Ac3Or more temperature T2(Ac3≤
T2), with heating temperature T2It keeps being allowed to austenitizing in 5~600 seconds.
It is heated to temperature T1Kept for 5 seconds or more.Preferably remaining the time is 900 seconds or less.In addition, keeping temperature T1, such as Fig. 1
[2], can also be in Ac1Point and 0.2 × Ac1+ 0.8 × Ac of point3It is kept at a temperature of fixation between point, for example, it is also possible to
Ac1Point and 0.2 × Ac1+ 0.8 × Ac of point3Be slowly heated between point etc., it is allowed in Ac1Point and 0.2 × Ac1+ 0.8 × Ac of point3Point
Between change.In this way, being kept by the relatively low temperature field in the two-phase coexisting region of ferrite and austenite, the iron coexisted
Among ferritic and austenite, Ovshinsky side is assigned to more Mn, and thus, it is possible to obtain Mn thickening region.Then, it is formed in this
Even if Mn thickening region, the Mn concentration after heat treatment as the remaining austenite of retained austenite are still high, it is possible thereby to plus
The deviation of the concentration of the Mn in big carbon thickening region can be realized height and swell formability.
If temperature T1Lower than Ac1The amount of point, the then austenite for having Mn to be thickened is few, in retained austenite (carbon thickening region)
The deviation of Mn concentration becomes smaller, and cannot obtain the formability that adequately swells.
If temperature T1Higher than 0.2 × Ac1+ 0.8 × Ac of point3Point, then the Mn concentration of austenite is lower, and (carbon is thick for retained austenite
Change region) in the deviation of Mn concentration become smaller, the formability that adequately swells cannot be obtained.
If temperature T1Under time of the retention time than 5 seconds it is short, then the time of Mn diffusion is insufficient, thickening of the Mn to austenite
Insufficient, the deviation of the Mn in retained austenite (carbon thickening region) becomes smaller, and cannot obtain the formability that adequately swells.
Preferable temperature T1Under retention time long aspect, but from the viewpoint of productivity, preferably 900 seconds or less.
Preferable temperature T1In 0.9 × Ac1+ 0.1 × Ac of point3Point and 0.3 × Ac1+ 0.7 × Ac of point3Between point, temperature T1Under
Retention time is 10 seconds or more and 800 seconds or less.More preferable temperature T1In 0.8 × Ac1+ 0.2 × Ac of point3Point and 0.4 × Ac1Point+
0.6×Ac3Between point, temperature T1Under retention time be 30 seconds or more and 600 seconds or less.
In addition, being used as in Fig. 1 shown in [1] to temperature T1Heating speed, preferably 5~20 DEG C/sec.
Secondly as shown in [4] of [3] of Fig. 1, it is warming up to Ac3Or more temperature T2(Ac3≤T2) and with temperature T2It keeps
And carry out austenitizing.Temperature T2Under retention time be 5~600 seconds.
By being heated to Ac3Or more temperature T2, it is being heated to temperature T1The ferritic part Shi Zuowei also becomes Ovshinsky
Body.Again the part Mn for mutually becoming austenite is not thickened.Therefore, there are the thickening regions of above-mentioned Mn in austenite, together
When there are the regions that Mn is not thickened, in high-strength steel sheet after heat treatment, retained austenite (carbon thickening region) can be increased
Mn concentration deviation, can be realized height and swell formability.
If temperature T2Lower than Ac3Point or temperature T2Under retention time it is shorter than 5 seconds, then the iron of obtained high-strength steel sheet
Ferritic divides rate to reduce higher than 5%, YR.
If temperature T2Excessively high, the Mn in the Mn thickening region being initially formed is spread, and the deviation of Mn concentration is possible to become
It is small.Therefore, temperature T2Preferably Ac3+ 50 DEG C or less of point.
If temperature T2Under retention time it is longer than 600 seconds, then due to spread cause Mn thickening region Mn concentration be lower, it is residual
The deviation of Mn concentration in remaining austenite becomes smaller, and the formability that swells reduces.
Preferable temperature T2For Ac3+ 10 DEG C or more of point, temperature T2Under retention time be 10~450 seconds.More preferable temperature T2
For Ac3+ 20 DEG C or more of point, temperature T2Under retention time be 20~300 seconds.
From temperature T shown in [3] of Fig. 11To temperature T2Heating, preferably with 0.1 DEG C/sec more than or lower than 10 DEG C/sec
Heating speed carries out.
In addition, about Ac1Point and Ac3Point is formed, by generally known calculation although can also be acquired by measurement with it
Formula, which calculate, to be advisable.
For example, Ac can be calculated with following (1) formulas and 2 (formulas)1Point and Ac3Point is (for example, referring to " Lesley's steel material
Material " ball is kind, (1985)).
Ac1Point (DEG C)=723+29.1 × [Si] -10.7 × [Mn]+16.9 × [Cr] -16.9 × [Ni] (1)
Ac3Point (DEG C)=910-203 × [C]1/2+ 44.7 × [Si] -30 × [Mn]+700 × [P]+400 × [Al]+
400 × [Ti]+104 × [V] -11 × [Cr]+31.5 × [Mo] -20 × [Cu] -15.2 × [Ni] (2)
Here, [] indicate the wherein described element with content shown in quality %.
(2) be cooled to 100 DEG C more than or lower than 300 DEG C between it is cooling stop temperature until
After above-mentioned austenitizing, as shown in [6] of Fig. 1, with 10 DEG C/sec or more of average cooling rate, it is cooled to 100
Cooling between DEG C more than or lower than 300 DEG C stops temperature T3Until.At 100 DEG C or more, lower than 300 DEG C within the temperature range of control
Refrigeration but stops temperature, so as to adjust the amount for not becoming martensite and remaining austenite mutually, controls final retained austenite
Amount.
In cooling, at least between 650 DEG C~300 DEG C, cooled down with 10 DEG C/sec of average cooling rate or more.Make to put down
Equal cooling velocity is 10 DEG C/sec or more, is to become fine geneva phosphor bodies to inhibit the ferritic formation in cooling
Tissue.
It as the preference of such cooling, can enumerate, as shown in [5] of Fig. 1, by 650 DEG C or more chillings
Start temperature T4, cooling (slow cooling) is carried out with 0.1 DEG C/sec of relatively low average cooling rate more than or lower than 10 DEG C/sec, such as
Shown in [6] of Fig. 1, from chilling start temperature T4To 300 DEG C or less cooling stopping temperature T3, with 10 DEG C/sec of average cooling rate with
On carry out cooling (chilling).In addition, by making chilling start temperature T4It is 650 DEG C or more, can inhibits in cooling (slow cooling)
Ferritic formation.
If cooling velocity is slower than 10 DEG C/sec, ferrite is formed, and YR is reduced.In addition, MA becomes thick, hole expansibility thus
It reduces.
If cooling stop temperature T3Lower than 100 DEG C, then remained austenite content is insufficient.As a result, although TS is got higher,
EL is reduced, TS × EL underbalance.
If cooling stop temperature T3It is 300 DEG C or more, then coarse non-transformed austenite increases, even if through cooling thereafter
Still remaining, final MA size becomes thick, and hole expansibility λ is reduced.
In addition, preferred cooling velocity is 15 DEG C/DEG C or more, more preferably 20 DEG C/s or more.Preferred cooling stopping temperature
Spend T3For 120 DEG C or more and 280 DEG C hereinafter, more preferably 140 DEG C or more and 260 DEG C or less.
As shown in [7] of Fig. 1, temperature T can also be stopped cooling3Lower holding.Preferred retention time when as holding,
It can enumerate 1~150 second.Even if the retention time is longer than 150 seconds, how the characteristic of obtained steel plate is not improved yet, steel plate
Productivity but reduces, therefore preferably at 150 seconds or less.
(3) until being again heated to 300 DEG C~500 DEG C of temperature range
As shown in [8] of Fig. 1, from above-mentioned cooling stopping temperature T3It rises with 30 DEG C/sec or more of reheating speed, heating
To the relation reheating temperature T for being in 300 DEG C~500 DEG C ranges5Until.By instant heating, it can shorten and can promote carbide
Precipitation and growth temperature field residence time, be able to suppress the formation of fine carbide.Preferably reheating speed is
60 DEG C/s or more, more preferably 70 DEG C/s.
Such instant heating, such as can reach in the method for high-frequency heating, electrified regulation etc..
Reach relation reheating temperature T5Afterwards, as shown in [9] of Fig. 1, with this temperature T5It keeps.At this moment, preferably make formula below
(1) the tempering parameter P represented by is 10000 or more and 14500 hereinafter, also, the retention time is 1~150 second.Present embodiment
Steel plate tempering parameter P by formula below (1) indicate.
P=T (K) × (20+log (t/3600) ... (1)
Here, T is tempering temperature (K), t is to maintain time (second).
When reheating, the carbon of super saturated solid solution is reallocated in martensite.It specifically, is exactly to occur following two
A phenomenon, that is, diffusion of the carbon from martensite to austenite;It is precipitated with the carbide (cementite) in the lath of martensite.This two
Among a phenomenon, if being kept for a long time under low temperature, it is easy to happen the precipitation of carbide.In addition, even if with high temperature dwell
When holding, if heating speed is slow or the retention time is too long, carbide can be also precipitated.On the other hand, carbon is from martensite to austenite
Diffusion, depend on diffusion velocity strongly, therefore the processing through the short time just can be carried out sufficiently at high temperature.
The particle for the cementite being present in martensite easily becomes the starting point of impact wreckage, becomes to drop impact resistant characteristic
Low reason.Therefore, when reheating, it is desirable to inhibit on one side the analysis of the carbide (cementite) in the lath of martensite
Out, promote reheating processing as diffusion of the carbon from martensite to austenite on one side.Therefore, effectively implement rapidly to add
The heat treatment of heat and high temperature and short time.
But it in order to make sufficient carbon spread generation obtain expected tensile strength, needs that temperature and time will be used as
Connector tempering parameter P control in a certain range.
If tempering parameter P, less than 10000, diffusion of the carbon from martensite to austenite does not occur sufficiently, and austenite becomes
It is unstable, it cannot ensure remained austenite content, therefore TS × EL underbalance.In addition, if tempering parameter P is greater than 14500, i.e.,
Make short time processing that can not prevent the formation of carbide, cannot ensure remained austenite content, TS × EL balance deterioration.In addition,
Even if tempering parameter is appropriate, if heating speed is too low, overlong time then still will form carbide in martensite lath, collision becomes
Cracking progress when shape is easy to happen, impact resistant deterioration in characteristics.The amount of carbide in martensite lath, can be according to small angle X
The scattering strength of ray scattering acquires.
If relation reheating temperature T5Lower than 300 DEG C, then Carbon diffusion is insufficient, cannot get enough remained austenite contents, and TS ×
EL is reduced.If relation reheating temperature T5Higher than 500 DEG C, then retained austenite resolves into cementite and ferrite, and retained austenite is not
Foot, characteristic cannot ensure.
If shorter than 1 second without holding or retention time, it is also possible to deficiencies for Carbon diffusion.It is therefore preferable that with again
Heating temperature T5Holding in progress 1 second or more.If the retention time is longer than 150 seconds, it is also possible to be precipitated as cementite for carbon.
Therefore, the retention time is preferably 150 seconds or less.
Preferred relation reheating temperature T5It is 320~480 DEG C, preferred relation reheating temperature T5It is 340~460 DEG C.
It is preferred that tempering parameter P is 10500~14500, at this moment the preferred retention time is 1~150 second.Preferred tempering
Parameter P is 11000~14000, and at this moment the preferred retention time is 1~100 second, more preferably 1~60 second.
After reheating, as shown in [10] of Fig. 1, such as such 200 DEG C of temperature below can be cooled to room temperature.As
200 DEG C of preferred average cooling rates below are cooled to, 10 DEG C/sec can be enumerated.
By above heat treatment, the high-strength steel sheet of embodiments of the present invention can be obtained.
If it is this field of the manufacturing method of the high-strength steel sheet for the embodiment for contacting present invention mentioned above
Then there is following possibility in technical staff, that is, can by trial and error method, with the manufacturing method different from above-mentioned manufacturing method,
Obtain the high-strength steel sheet of embodiments of the present invention.
[embodiment]
1. sample makes
The casting material is hot-forged after manufacturing the casting material with chemical composition described in table 1 by vacuum melting
And after becoming the steel plate of plate thickness 30mm, implement hot rolling.In addition, also describing the with good grounds calculated Ac of composition in table 13Point.
The condition of hot rolling will not apply influence substantially to the final tissue and characteristic of this patent, be heated to 1200 DEG C
Afterwards, reach plate thickness 2.5mm through multistage rolling.At this moment, the end temperature of hot rolling is 880 DEG C.Thereafter, 600 are cooled to 30 DEG C/sec
DEG C, stop cooling, after insertion is heated in 600 DEG C of furnace, is kept for 30 minutes, thereafter, progress furnace is cold, as hot rolled steel plate.
After the oxide skin for removing surface to hot rolled steel plate implementation pickling, implementation is cold-rolled to 1.4mm.To the cold-reduced sheet into
Row heat treatment, obtains sample.Heat treatment condition is shown in table 2.In addition, such as [2] are shown in [] in this way in table 2
Number, it is corresponding with the process being identically numbered being shown in Fig. 1 in [].
In table 2, in sample No.1, austenitizing temperature T is not divided into1With temperature T2Two stages carry out, only with suitable
In temperature T2Ac3Or more temperature keep.
Sample No.9 is (to be to skip in Fig. 1 with the sample that this temperature is kept after being cooled to relation reheating temperature and be equivalent to [7]
The sample of the process of~[8]), with substitution be cooled to 100 DEG C more than or lower than 300 DEG C between cooling stop temperature.
Sample 15 and 31~36 is to make heating temperature T2With chilling start temperature T4Identical sample.That is, being in austenite
After change, a stage is cooled to cooling stopping temperature T3Until sample.
The reheating for being equivalent to [8] is carried out by electrified regulation method.
In addition, in 1~table of table 4, the numerical value with asterisk (*), indicate to be detached from embodiments of the present invention range it
Outside.
[table 1]
[table 2]
2. structure of steel
The total of ferrite point rate, tempered martensite and tempering bainite is acquired according to the above method for each sample
Rate is divided (to describe the Mn for being thickened region for " tempering M/B "), remained austenite content (remaining γ amount), the average-size of MA, carbon in table 3
The half breadth of concentration distribution and the q value of small angle X ray scattering are 1nm- 1Scattering strength.The measurement of remained austenite content
In, use Co., Ltd.'s リ ガ Network two dimension zone X ray detecting diffraction device (RINT-RAPIDII).Obtain as the result is shown in table
In 3.
In addition, in the present embodiment, the structure of steel (residue tissue) other than structure of steel described in table 3 removes sample No.9
Sample in addition is the martensite not being tempered, and sample No.9 is the bainite not being tempered.
[table 3]
3. mechanical property
YS, TS, EL are measured using cupping machine for obtained sample, calculate YR and TS × EL.In addition, according to upper
The method stated acquire hole expansibility λ, limit bulging height (bulging height), the cross tensile strength of spot-welding part (stretching of SW cross) and
R5 stretches plate thickness reduction.Obtain as the result is shown in table 4.
[table 4]
The result of investigation table 4.Sample No.12~15,18,21 and 29~36 are to meet in embodiments of the present invention to advise
The embodiment of fixed whole important documents (composition, manufacturing condition and structure of steel).The tension that these samples reach 980MPa or more is strong
Spend (TS), 0.75 or more yield tensile ratio (YR), TS × EL of 20000MPa% or more, 20% or more hole expansibility (λ), the limit is swollen
Shape height is 16mm or more, the SW cross of 6kN or more stretches and 50% or more R5 stretches plate thickness reduction (RA).
In contrast, austenitizing is not divided into temperature T in sample No.11With temperature T2Two stages carry out, only with
It is equivalent to temperature T2Ac3Or more temperature keep, therefore carbon thickening region Mn concentration distribution half breadth value
Small, limit bulging height is low.In addition, carbide (cementite) is precipitated because [7] retention time is up to 300 seconds.In addition,
Because the scattering strength of small angle X ray scattering is big, the volume fraction of the cementite of about 1nm is big.As a result, resistance to touch
Hit characteristic (plate thickness reduction) reduction.
In sample No.2, because keeping temperature T1It is low, so the half breadth of the concentration distribution of the Mn in carbon thickening region
It is worth small, limit bulging height is lower.
In sample No.3, because keeping temperature T1Height, so the half breadth of the concentration distribution of the Mn in carbon thickening region
Value it is small, limit bulging height is low.Furthermore [7] retention time is up to 300 seconds, therefore carbide (cementite) is precipitated.In addition, by
It is big in the scattering strength of small angle X ray scattering, so the volume fraction of the cementite of about 1nm is big.As a result, impact resistant
Characteristic (plate thickness reduction) reduces.
In sample No.4 and 5, because being heated to heating temperature T1And after keeping, selection and T1Identical temperature is as heating
Temperature T2, so austenitizing cannot be carried out with sufficiently high temperature.Therefore, ferrite content is more, tempered martensite and tempering shellfish
The total of family name's body divides rate low, and the value of the half breadth of the concentration distribution of the Mn in carbon thickening region becomes smaller.As a result, tension is strong
Degree, yield tensile ratio and limit bulging height are lower.
In sample No.6, heating temperature T2Low, ferrite quantitative change is more, as a result, yield tensile ratio is lower.
In sample No.7, because cooling stop temperature T3Height, so tempered martensite and the total of tempering bainite divide rate
It is low, and the average-size of MA is big.As a result, hole expansibility is lower.
In sample No.8, because of heating temperature T1Under retention time it is short, so the concentration point of the Mn in carbon thickening region
The value of the half breadth of cloth is small, as a result, limit bulging height is lower.
In sample No.9, heating temperature T2Under retention time it is long, it is in addition cooling to stop temperature T3It is high.Therefore, tempered martensite
Body and the total of tempering bainite divide the average-size that rate is 0%, MA big, and the value of the half breadth of the concentration distribution of Mn becomes
It is small.As a result, tensile strength, hole expansibility and limit bulging height are low.In addition, because ([9] are protected within 300 seconds with the holding of this temperature
Hold the time), so the formation of carbide is also few.These are the result is that hole expansibility λ is reduced.
It is cooling to stop temperature T in sample No.103Low, remained austenite content is few, as a result, the value and the limit of TS × EL
Bulging height is lower.
In sample No.11, because [8] reheat speed slowly up to 30 DEG C/sec, carbide (cementite) is precipitated.In addition,
Since the scattering strength of small angle X ray scattering is big, so the volume fraction of the cementite of about 1nm is big.As a result, resistance to touch
Hit characteristic (plate thickness reduction) reduction.
In sample No.16, because of chilling start temperature T4It is low, so ferrite content is more, tempered martensite and tempering bayesian
The total of body divides rate low.As a result, tensile strength and yield tensile ratio are low.In addition, be up to 300 seconds because of [9] retention time,
Carbide (cementite) is precipitated.In addition, the scattering strength due to small angle X ray scattering is big, so the volume of the cementite of about 1nm
Point rate is big.As a result, impact resistant characteristic (plate thickness reduction) reduces.
In sample No.17, because [8] reheat speed slowly up to 15 DEG C/sec, carbide (cementite) is precipitated.In addition,
Since the scattering strength of small angle X ray scattering is big, so the volume fraction of the cementite of about 1nm is big.As a result, resistance to touch
Hit characteristic (plate thickness reduction) reduction.
In sample No.19, relation reheating temperature T5Height, therefore parameter is up to 14604, remained austenite content is few.As a result,
The value and limit bulging height of TS × EL is lower.In addition, the scattering strength due to small angle X ray scattering is big, so the infiltration of about 1nm
The volume fraction of carbon body is big.As a result, impact resistant characteristic (plate thickness reduction) reduces.
In sample No.20, relation reheating temperature T5It is low, therefore parameter, down to 9280, remained austenite content tails off.Its result
It is that the value and limit bulging height of TS × EL is lower.
In sample No.22, C amount is low, and remained austenite content is few, as a result, the value of TS × EL and limit bulging height become
It is low.
In sample No.23, Mn amount is more, and remained austenite content is few, as a result, the value of TS × EL and limit bulging height become
It is low.
In sample No.24, Mn amount is few, and ferrite content is more, and the total amount of tempered martensite and tempering bainite is insufficient.It is tied
Fruit is that tensile strength and yield tensile ratio are lower.
In sample No.25, Si+Al amount is low, and tempered martensite and the total of tempering bainite divide rate and remained austenite content
Low, MA is average to be become large-sized.As a result, the value of TS × EL, hole expansibility and limit bulging height are lower.
In sample No.26, C amount is more, as a result, SW cross tensile strength is lower.
In sample No.27, Si+Al amount is more, as a result, the value of TS × EL and limit bulging height are lower.
In sample No.28, because keeping temperature T1Height, so the half breadth of the concentration distribution of the Mn in carbon thickening region
Value it is small, limit bulging height is lower.
4. summarizing
In this way, meeting the steel plate of composition and structure of steel as defined in embodiments of the present invention, it is able to confirm that tensile strength
(TS), fracture when yield tensile ratio (YR), the product (TS × EL) of (TS) and breaking elongation (EL), hole expansibility (λ), tension test
The cross tensile strength of plate thickness reduction (RA), limit bulging height and spot-welding part is in high level.
It additionally is able to confirm, the manufacturing method of embodiment according to the present invention can manufacture and meet implementation of the invention
The composition of mode defined and the steel plate of structure of steel.
The application with the applying date for the Japanese Patent Application on the 3rd of August in 2016, Patent 2016-153110 with
The claim of priority of basis application.Patent 2016-153110 is incorporated into this specification due to reference.
Claims (6)
1. a kind of high-strength steel sheet, contains
The C:0.15 mass mass of %~0.35 %,
Si's and Al is total: 0.5 mass of mass %~3.0 %,
The Mn:1.0 mass mass of %~4.0 %,
P:0.05 mass % or less,
S:0.01 mass % hereinafter,
Surplus is made of Fe and inevitable impurity,
In structure of steel,
Ferrite divide rate be 5% hereinafter,
Tempered martensite and the total of tempering bainite divide rate to be 60% or more,
Remained austenite content is 10% or more,
The average-size of MA 1.0 μm or less,
Half breadth with the concentration distribution of the Mn in the carbon thickening region of remained austenite content equivalent is 0.3 mass % or more,
The q value of small angle X ray scattering is 1nm- 1Scattering strength in 1.0cm- 1Below.
2. high-strength steel sheet according to claim 1, wherein C amount is 0.30 mass % or less.
3. high-strength steel sheet according to claim 1 or 2, wherein Al amount is lower than 0.10 mass %.
4. a kind of manufacturing method of high-strength steel sheet, wherein comprise the following steps:
Prepare the process of rolled stock, the rolled stock contains the total of the C:0.15 mass mass of %~0.35 %, Si and Al: 0.5
Mass %, Mn:1.0 mass mass %, the P:0.05 mass of %~4.0 of quality %~3.0 % or less, S:0.01 mass % hereinafter,
Surplus is made of Fe and inevitable impurity;
By the rolled stock in Ac1Point and 0.2 × Ac1+ 0.8 × Ac of point3After being kept for 5 seconds or more at a temperature of between point, it is heated to
Ac3Or more temperature and kept for 5~600 seconds and the process that carries out austenitizing;
After the austenitizing, 100 DEG C are cooled to 10 DEG C/sec or more of average cooling rate from 650 DEG C or more of temperature
The process until cooling stopping temperature between more than or lower than 300 DEG C;
It is heated to 30 DEG C/sec or more of average heating rate in 300 DEG C~500 DEG C ranges from the cooling stopping temperature
Relation reheating temperature until process;
At the relation reheating temperature T, to meet the tempering parameter P of formula (1) defined for 10000~14500 and retention time t
The process kept for 1~150 second mode;With
After the holding, from the relation reheating temperature until 10 DEG C/sec or more of average cooling rate is cooled to 200 DEG C
Process,
P=T × (20+log (t/3600)) ... (1)
Here, T: relation reheating temperature, unit K;T: retention time, unit are the second.
5. the manufacturing method of high-strength steel sheet according to claim 4, wherein cold until the cooling stopping temperature
But in, comprising: be cooled to the urgency of 650 DEG C or more of temperature with 0.1 DEG C/sec of average cooling rate more than or lower than 10 DEG C/sec
Process until cold start temperature;Institute is cooled to from the chilling start temperature with 10 DEG C/sec of average cooling rate or more
State the process until cooling stopping temperature.
6. the manufacturing method of high-strength steel sheet according to claim 4 or 5, wherein the tempering parameter be 11000~
14000, the retention time is 1~150 second.
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JP2016153110A JP6762798B2 (en) | 2016-08-03 | 2016-08-03 | High-strength steel sheet and its manufacturing method |
JP2016-153110 | 2016-08-03 | ||
PCT/JP2017/026569 WO2018025675A1 (en) | 2016-08-03 | 2017-07-21 | High-strength steel plate and manufacturing method thereof |
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CN109477182B CN109477182B (en) | 2021-06-18 |
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US (1) | US20190185958A1 (en) |
EP (1) | EP3495523B1 (en) |
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DE102018132816A1 (en) * | 2018-12-19 | 2020-06-25 | Voestalpine Stahl Gmbh | Process for the production of thermo-mechanically produced profiled hot-rolled products |
DE102018132860A1 (en) * | 2018-12-19 | 2020-06-25 | Voestalpine Stahl Gmbh | Process for the production of conventionally hot-rolled, profiled hot-rolled products |
DE102018132908A1 (en) * | 2018-12-19 | 2020-06-25 | Voestalpine Stahl Gmbh | Process for the production of thermo-mechanically produced hot strip products |
DE102018132901A1 (en) * | 2018-12-19 | 2020-06-25 | Voestalpine Stahl Gmbh | Process for the production of conventionally hot rolled hot rolled products |
WO2020138343A1 (en) * | 2018-12-27 | 2020-07-02 | 日本製鉄株式会社 | Steel sheet |
JP7185555B2 (en) * | 2019-02-18 | 2022-12-07 | 株式会社神戸製鋼所 | steel plate |
WO2022044492A1 (en) * | 2020-08-27 | 2022-03-03 | 日本製鉄株式会社 | Hot-rolled steel sheet |
EP4206344A4 (en) * | 2020-08-27 | 2023-12-13 | Nippon Steel Corporation | Hot-rolled steel sheet |
MX2023002219A (en) * | 2020-08-27 | 2023-03-07 | Nippon Steel Corp | Hot-rolled steel sheet. |
MX2023002114A (en) * | 2020-08-27 | 2023-03-15 | Nippon Steel Corp | Hot-rolled steel sheet. |
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- 2017-07-21 US US16/321,157 patent/US20190185958A1/en not_active Abandoned
- 2017-07-21 CN CN201780046036.5A patent/CN109477182B/en not_active Expired - Fee Related
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CN109477182B (en) | 2021-06-18 |
JP6762798B2 (en) | 2020-09-30 |
JP2018021233A (en) | 2018-02-08 |
EP3495523A4 (en) | 2020-02-26 |
WO2018025675A1 (en) | 2018-02-08 |
EP3495523A1 (en) | 2019-06-12 |
US20190185958A1 (en) | 2019-06-20 |
EP3495523B1 (en) | 2021-06-30 |
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