TECHNICAL FIELD
[0001] The present invention relates to the technical field of automobile steel, in particularly
to a high-plasticity hot-forming steel with oxidation resistance for automobiles and
a hot-forming process thereof.
BACKGROUND ART
[0002] In recent years, new materials for car body have been continuously developed and
applied to car bodies. However, ultra-high strength steel plates for cold stamping
at strength levels above 1000 MPa are often used for manufacturing components with
simple shapes due to the constraints of easy cracking and large springback. However,
the hot-forming steel is formed in an austenite zone by using hot-forming process,
and has small springback, which can meet the requirements of assembly accuracy. Through
pressure-holding and quenching, the ultra-high strength components of 1500 MPa level
and above can be obtained, which effectively simplifies the design of body structure
and parts, and greatly reduces the weight of the vehicle.
[0003] At present, hot-forming steels on the market can be classified as coated hot-forming
steels and uncoated hot-forming steels according to their surface conditions. The
uncoated steel is easy to form scale on its surface and suffers from decarburization
when being heated in a heating furnace, which affects the performance of the steel;
therefore, it is necessary to use protective atmosphere during heating of the hot-forming
steel, and to make the shot peening treatment after hot forming, which increases the
cost and working procedures. While the coated steel has an aluminum-silicon coating
or zinc-based coating on the surface of the steel plate, which can effectively prevent
the steel from surface decarburization and oxidation during heating, and the steel
after hot forming can be exempted from the shot peening process, but the cost of the
coated hot-forming steel is higher than the uncoated steel. At present, the strengthen
level used for mass production and use of the hot-forming steel in the prior art is
1500 MPa; however, the elongation of the hot-forming steel after hot forming is only
about 6-9%, which cannot meet the development requirements of the automotive field,
and no better technology is available to keep a lower cost of the hot-forming steel,
to solve the problem of surface oxidation and decarburization of the steel after hot
forming, and to avoid the shot peening process, moreover, the hot-forming steel also
has higher plasticity after hot forming.
[0004] The patent with the Publication No. being
CN107354385B proposes a method for preparing an ultra-high strength hot-forming steel for automobiles.
Chemical compositions of the steel include C: 0.5-0.6%, Mn: 0.5%-2.0%, Si: 1.5%-2.5%,
Cr: 1.0%-3.0%, Al: 1.0%-2.0%, Nb: 0.01%-0.03%, and B: 0.001%-0.005%. The strength
of the steel plate after hot forming reaches 1500-2000MPa, and the elongation is 10%-20%.
The steel plate proposed in the patent has good strength-plasticity compatibility,
but Cr and Al elements are higher in its compositions, which increases the cost and
smelting difficulty. At the same time, the production process is complex, the existing
tooling and equipment do not meet the production requirements, and the production
also requires atmosphere protection and shot peening.
[0005] The patent with Publication No. being
CN103255340B proposes a hot-forming steel plate with high strength and toughness for automobiles
and a preparation method thereof. Chemical compositions of the steel sheet include
C: 0.1-0.5%, Si: 0.5-1.5%, Mn: 1.2-2.4%, Ti: 0.01-0.05%, B: 0.001-0.005%, S: ≥0.01%,
and P: ≥0.01%. After hot forming, the tensile strength of the steel plate reaches
1600MPa and the elongation reaches 16%, proving good comprehensive performance and
relatively low alloy cost. However, the steel plate needs to be deformed during heating
process, and then quenched twice to obtain the final microstructure and mechanical
properties, which involves a complicated hot-forming process and is unable to be implemented
through the existing equipment, moreover, it also needs gas protection during heating,
and needs shot peening after hot forming.
[0006] To sum up, the development of high-plasticity hot-forming process with good oxidation
resistance and the hot-forming technology for automobiles has good application prospects.
SUMMARY
[0007] According to the above technical problems, the present invention provides a high-plasticity
hot-forming steel with oxidation resistance for automobiles and a hot-forming process
thereof.
[0008] A technical solution adopted by the present invention is as follows:
A high-plasticity hot-forming steel with oxidation resistance for automobiles, where
the hot-forming steel has chemical compositions in mass percentages as follows:
C: 0.18%-0.28%, Si: ≥0.20%, Mn: 1.20%-2.0%, P: 0.030%-0.080%, S≥0.004%, Als: 0.02%-0.06%,
Nb: 0.02%-0.06%, Ti: 0.025%-0.045%, V: 0.05%-0.15%, Cr: 0.5%-2.50%, Mo: 0.10%-0.30%,
B: 0.0015%-0.0035%, N≥0.005%, the balance Fe and inevitable impurities.
[0009] A microstructure of the hot-forming steel includes a ferrite, a martensite and a
retained austenite. The ferrite has a volume fraction of 5%-12%, the martensite has
a volume fraction of 78%-89%, and the retained austenite has a volume fraction of
6%-10%.
[0010] A tensile strength of the hot-forming steel is 1400MPa-1700MPa, an oxidation resistance
rate of the hot-forming steel is < 0.1g/(m
2·h), a yield strength of the hot-forming steel is 900MPa-1450 MPa, an elongation of
the hot-forming steel is ≤18.0%, a surface of the hot-forming steel is not completely
decarburized with a thickness of decarburized layer ≥15 µm, and a thickness of the
hot-forming steel is 0.8mm-12.0mm.
[0011] Main role of the composition of the steel disclosed in the present invention is as
follows:
C: C is the guarantee of steel strength, which is beneficial to improving hardenability
of the steel. If the carbon content is too low, the strength of the steel after hot
stamping cannot reach the expected target. If the carbon content is too high, the
strength of the steel after hot forming will be too high, and the plasticity will
thus decrease. In addition, the increase of C content can reduce the phase transition
temperature, so the austenitizing temperature will be lowered, which is beneficial
to obtaining a shot blasting-free surface. At the same time, the increase of C content
is beneficial to generating sufficient content of undercooled austenite during pressure
holding of the hot-forming process and to improving the plasticity. Therefore, the
optimal range of C in the present invention is 0.18%-0.28%.
Si: Si is an element without carbide precipitation in steel, which has a good inhibiting
effect on carbide precipitation during cooling and pressure holding of the hot-forming
process, thereby ensuring the content and stability of retained austenite. However,
if the Si content is too high, a large number of defects such as scale and color difference
will appear on the surface of the hot-forming substrate, which will affect the surface
quality of hot-forming parts. At the same time, too high Si content will enlarge the
two-phase region, raise the austenitizing temperature, and make the steel keep warm
at a higher temperature, which is easy to deteriorate the surface of the steel. Therefore,
the Si content in the steel proposed in the present invention is ≥0.20%.
Mn: Main role of Mn in the present invention is to improve the hardenability of the
steel and reduce the phase transition temperature, so that the austenitization of
the steel can be realized at a lower temperature. Too high content of Mn will deteriorate
the microstructure uniformity of the steel, and easily cause serious banded structural
defects in the microstructure. Therefore, the selected Mn content in the present invention
is 1.20%-2. 0%.
P: The role of P in the present invention is similar to that of Si, which can inhibit
the formation of cementite and increase the stability of residual austenite. Also,
P can have martensite laths refined, distribute it evenly and improve the toughness.
The P content in the present invention is 0.030%-0.080%.
S: S is a harmful element in the present invention, and S will form MnS inclusions,
which will deteriorate the microstructure and mechanical properties of the steel.
Therefore, S is limited to ≥0.004% in the present invention.
Als: Als (acid-soluble aluminum) plays a role of deoxidization and nitrogen fixation
in the smelting process, but too much Als will give rise to a large number of aluminum-based
inclusions. Therefore, the Als content in the present invention is 0.020%-0.060%.
Cr: Cr is an element for improving the hardenability of the steel. In the present
invention, main role of Cr is to improve the high-temperature oxidation resistance
of the steel and simultaneously improve the tempering stability of the steel, so as
to ensure that the steel does not appear tempered martensite within the pressure-holding
temperature range. The optimum Cr content falls between 0.5% and 2.50%.
Mo: Mo is a medium-strong carbide forming element that can improve the strength and
toughness of the steel. In the present invention, Mo can lower the martensitic transformation
temperature, significantly improve the stability of retained austenite, and at the
same time, the addition of Mo element improves the oxidation resistance of the steel.
The Mo content in the present invention is 0.10%-0.30%.
Nb, V: Nb and V mainly play the role of fine grain strengthening and precipitation
strengthening in steel. In the present invention, Nb and V can effectively pin the
original austenite grain boundary by diffusely precipitating the nano-scale fine carbides,
thereby refining the structure of each phase in the hot-forming steel and improving
the comprehensive performance. At the same time, the diffusely precipitated carbides
can act as hydrogen traps to pin the diffusable hydrogen in the steel, which can improve
the delayed fracture resistance of the steel. In addition, VN precipitation formed
by V and N can inhibit BN precipitation and avoid the strength reduction caused by
B precipitation. In the present invention, the Nb content is 0.020%-0.060%, and the
V content is 0.050%-0.15%.
Ti: Ti is mainly used for fixing nitrogen in boron steel to ensure that the quenching
effect of boron can be exerted. In addition, Ti can also form fine carbide precipitation
with C element, which reduces the hardness and strength of martensite in the structure
after hot forming, and is beneficial to improving the plasticity and toughness of
the steel. The Ti content in the present invention falls between 0.025% and 0.045%.
B: Adding boron to the steel can significantly improve the hardenability of the steel
and ensure the stability of steel strength after quenching. Too low B content makes
the effect insignificant, while too high B content it is easy to form B compounds
with N in the steel, which will reduce the performance of the steel. The B content
in the present invention is 0.0015%-0.0035%.
N: The lower the N content is, the better it becomes, but too low content of N will
lead to production difficulties and increase the cost, so the N content in the present
invention is ≥0.005%.
[0012] In the present invention, by adding alloying elements such as C, Mn, Cr, Mo, etc.,
the austenitizing temperature is lowered, the hardenability of the steel is improved,
and the oxidation of the steel is propitious to be inhibited. At the same time, the
critical cooling rate of the steel after hot forming is reduced, and is beneficial
to the production of thick-specification hot-forming steel. In addition, through the
combination of chemical composition and hot-forming process, a certain content of
ferrite can be obtained in the air-cooling stage, and a certain content of retained
austenite with good stability can be obtained in the pressure-holding stage after
cooling, which improves the plasticity of the steel. The addition of Si and P elements
in the composition inhibits the precipitation of carbides, which guarantees the content
of retained austenite in the steel and improves the mechanical properties of the steel.
In addition, the Cr and Mo elements in the steel composition play an anti-oxidation
role, so that the steel can be heated and kept warm under the condition of having
no protective atmosphere, and can be subjected to the subsequent processes after hot
forming directly without shot peening.
[0013] The present invention also discloses a hot-forming process of high-plasticity hot-forming
steel with oxidation resistance for automobiles, including the following steps of:
- (1) placing the hot-forming substrate containing the above compositions into a heating
furnace at a temperature of AC3-AC3+15°C for heating and heat preservation for a period of 180s-300s;
- (2) taking the heated hot-forming steel out of the heating furnace for air cooling
to a temperature of Ar3 and staying for 5s-8s before being put into a hot-forming mold for deformation and
cooling, at a cooling rate of ≤18°C/s, performing the pressure holding for 40s-80s
after cooling to 180°C-250°C, and taking out the formed parts for air-cooling to room
temperature after pressure holding to obtain the hot-forming steel.
[0014] The steel does not need atmosphere protection during hot forming, does not need shot
blasting treatment after hot forming, and can be subjected to the subsequent processes
directly, and the whole process cost of the steel plate is lower than that of the
existing hot-forming products.
[0015] The above hot-forming substrate is obtained after smelting, hot rolling and cold
rolling. The smelted composition and the mass percentage thereof are the composition
and mass percentage of the aforesaid high-plasticity hot-forming steel with oxidation
resistance for automobiles.
[0016] Compared with the prior art, the present disclosure has the following advantages:
- (1) through the combination of chemical composition and hot-forming process provided
in the present invention, a certain amount of ferrite and retained austenite structure
are introduced into traditional whole martensitic structure to improve the plasticity
of steel, so that the elongation of steel reaches to or exceeds 18% and the tensile
strength is more than 1400MPa;
- (2) by adding Cr or other elements, the oxidation resistance of the steel is improved,
the oxidation resistance rate of the steel is <0.1g/(m2•h), the oxidation resistance level reaches Level 1, and the steel does not need atmosphere
protection during hot forming, does not need shot blasting treatment after hot forming
and can be subjected to the subsequent processes directly; and
- (3) the proposed hot-forming steel and hot-forming process can be implemented through
the existing equipment, without equipment modification and at a relatively low cost.
[0017] Based on the above reasons, the present invention can be widely popularized in the
fields of automobile steel and the like.
DETAILED DESCRIPTION OF THE EMBODIMENTS
[0018] It should be noted that the embodiments of the present invention and features in
the embodiments, under the condition of no conflict, can be combined with each other.
The described embodiments are some, rather than all of the embodiments of the present
disclosure. The following description of at least one example embodiment is merely
illustrative in nature, and is in no way intended to limit the present disclosure,
an application or use thereof. Based on the embodiments of the present disclosure,
all other embodiments acquired by those of ordinary skill in the art without making
creative efforts fall within the scope of protection of the present disclosure
[0019] The present invention provides a high-plasticity hot-forming steel with oxidation
resistance for automobiles, where the hot-forming steel has chemical compositions
in mass percentages as follows: C:
C: 0.18%-0.28%, Si: ≥0.20%, Mn: 1.20%-2.0%, P: 0.030%-0.080%, S≥0.004%, Als: 0.02%-0.06%,
Nb: 0.02%-0.06%, Ti: 0.025%-0.045%, V: 0.05%-0.15%, Cr: 0.5%-2.50%, Mo: 0.10%-0.30%,
B: 0.0015%-0.0035%, N≥0.005%, the balance Fe and inevitable impurities.
[0020] A microstructure of the hot-forming steel includes a ferrite, a martensite and a
retained austenite. The ferrite has a volume fraction of 5%-12%, the martensite has
a volume fraction of 78%-89%, and the retained austenite has a volume fraction of
6%-10%.
[0021] The hot-forming steel has a tensile strength of 1400MPa-1700MPa, an oxidation resistance
rate <0.1g/(m
2·h), a yield strength of 900MPa-1450MPa, and an elongation ≤18.0%. The surface of
the steel is not completely decarburized with a thickness of decarburized layer ≥15
µm, and the hot-forming steel has a thickness of 0.8-12.0mm.
[0022] After smelting, hot rolling and cold rolling, the high-strength hot-forming steel
with excellent oxidation resistance provided in this embodiment obtains a hot-forming
substrate with a thickness of 0.8-12.0mm. Then, a hot-forming process is performed,
and the hot-forming process includes the following steps:
- (1) the hot-forming substrate containing the above compositions is placed into a heating
furnace at a temperature of AC3-AC3+15°C for heating and heat preservation for a period of 180s-300s; and
- (2) the heated hot-forming steel is taken out of the heating furnace for air cooling
to a temperature of Ar3 and stayed for 5s-8s before being put into a hot-forming mold for deformation and
cooling, at a cooling rate of ≤18°C/s, the pressure holding is performed for 40s-80s
after cooling to 180°C-250°C, and the formed parts is taken out for air cooling to
room temperature after pressure holding to obtain the hot-forming steel.
[0023] The compositions, hot-forming process parameters, and the microstructure and performance
of the steel after hot forming of the embodiments of the present invention are shown
in Tables 1 to 3.
Table 1 Composition of Embodiment of the Present Invention (wt, %)_
| Embodiment |
C |
Si |
Mn |
P |
S |
Als |
Nb |
V |
Ti |
Cr |
Mo |
B |
N |
| 1 |
0.18 |
0.20 |
20 |
0.08 |
0.003 |
0.035 |
0.030 |
0.15 |
0.045 |
210 |
0.15 |
0.0035 |
0.003 |
| 2 |
0.21 |
0.10 |
1.90 |
0.06 |
0.002 |
0.020 |
0.060 |
0.13 |
0.038 |
1.90 |
0.20 |
0.0030 |
0.004 |
| 3 |
0.23 |
0.15 |
1.70 |
0.05 |
0.003 |
0.035 |
0.045 |
0.090 |
0.025 |
1.60 |
0.25 |
0.0027 |
0.003 |
| 4 |
0.25 |
0.08 |
1.80 |
0.045 |
0.002 |
0.040 |
0.050 |
0.070 |
0.032 |
1.20 |
0.30 |
0.0015 |
0.002 |
| 5 |
0.27 |
0.05 |
1.50 |
0.035 |
0.004 |
0.055 |
0.035 |
0.060 |
0.028 |
0.80 |
0.17 |
0.0025 |
0.005 |
| 6 |
0.28 |
0.02 |
1.20 |
0.030 |
0.003 |
0.060 |
0.020 |
0.050 |
0.029 |
0.50 |
0.10 |
0.0018 |
0.001 |
| 7 |
0.22 |
0.17 |
1.35 |
0.065 |
0.002 |
0.027 |
0.055 |
0.11 |
0.035 |
250 |
0.20 |
0.0032 |
0.004 |
| 8 |
0.26 |
0.001 |
1.60 |
0.075 |
0.001 |
0.032 |
0.040 |
0.080 |
0.042 |
230 |
0.28 |
0.0024 |
0.003 |
Table 2 Hot-forming Process of Embodiment of the Present Invention
| Embod iment |
AC3, °C |
Heating Temperature, °C |
Heat Preservati on Period, s |
Residence Time of temperatur e Ar3, s |
Cooling Rate, °C/s |
Pressure-holdi ng Temperature, °C |
Pressure-holdi ng Time, s |
| 1 |
853 |
860 |
180 |
8 |
22 |
250 |
80 |
| 2 |
841 |
850 |
200 |
5 |
25 |
180 |
60 |
| 3 |
837 |
850 |
220 |
7 |
27 |
200 |
40 |
| 4 |
829 |
840 |
240 |
6 |
21 |
210 |
50 |
| 5 |
818 |
830 |
260 |
6 |
24 |
220 |
65 |
| 6 |
812 |
825 |
280 |
5 |
19 |
245 |
75 |
| 7 |
840 |
855 |
300 |
6 |
19 |
190 |
70 |
| 8 |
824 |
835 |
300 |
7 |
18 |
230 |
55 |
Table 3 Microstructure and performance parameters of Embodiment of the Present Invention
| Embodi ment |
Thickne ss, mm |
Yield strengt h, MPa |
Tensil e strengt h, MPa |
A (elongation ) , % |
Volum e fractio n of ferrite , % |
Volume fraction of martensit e, % |
Volume fraction of austenite , % |
Oxidat ion resista nce rate, g/(m2· h) |
Thickne ss of decarbur ized layer, µm |
| 1 |
0.8 |
900 |
1400 |
230 |
12 |
78 |
10 |
0.08 |
12 |
| 2 |
1.2 |
1230 |
1590 |
20.0 |
7 |
86 |
7 |
0.07 |
8 |
| 3 |
2.0 |
1050 |
1470 |
230 |
10 |
82 |
8 |
006 |
7 |
| 4 |
3.5 |
1140 |
1540 |
220 |
9 |
83 |
8 |
0.07 |
13 |
| 5 |
4.5 |
1360 |
1650 |
21.5 |
6 |
85 |
9 |
0.05 |
15 |
| 6 |
7.0 |
1450 |
1700 |
180 |
5 |
89 |
6 |
0.05 |
3 |
| 7 |
9.0 |
950 |
1480 |
190 |
8 |
85 |
7 |
0.08 |
10 |
| 8 |
12.0 |
1200 |
1580 |
25.0 |
7 |
84 |
9 |
0.09 |
6 |
[0024] Through the combination of chemical composition and hot-forming process provided
in the embodiment of the present invention, a certain amount of ferrite and retained
austenite structure are introduced into traditional whole martensitic structure to
improve the plasticity of steel, so that the elongation of steel reaches to or exceeds
18% and the tensile strength is more than 1400MPa. By adding Cr, Mo and other elements,
the oxidation resistance of the steel is improved, the oxidation resistance rate of
the steel is <0.1g/(m
2·h), the oxidation resistance level reaches Level 1, and the steel does not need atmosphere
protection during hot forming, does not need shot blasting treatment after hot forming,
and can be subjected to the subsequent processes directly. Moreover, the proposed
hot-forming steel and hot-forming process is lower in the whole process cost than
that of the existing hot-forming products, and can be implemented through the existing
equipment, without equipment modification.
[0025] At last, it should be noted that the above various embodiments are merely intended
to illustrate the technical solution of the present disclosure and not to limit the
same; although the present disclosure has been described in detail with reference
to the foregoing embodiments, it should be understood by those ordinary skilled in
the art that the technical solutions described in the foregoing embodiments may be
modified or equivalents may be substituted for some or all of the technical features
thereof; and the modification or substitution does not make the essence of the corresponding
technical solution deviate from the scope of the technical solution of each embodiment
of the present disclosure.
1. A high-plasticity hot-forming steel with oxidation resistance for automobiles, wherein
the hot-forming steel has chemical compositions in mass percentages as follows:
C: 0.18%-0.28%, Si: ≥0.20%, Mn: 1.20%-2.0%, P: 0.030%-0.080%, S≥0.004%, Als: 0.02%-0.06%,
Nb: 0.02%-0.06%, Ti: 0.025%-0.045%, V: 0.05%-0.15%, Cr: 0.5%-2.50%, Mo: 0.10%-0.30%,
B: 0.0015%-0.0035%, N≥0.005%, the balance Fe and inevitable impurities.
2. The high-plasticity hot-forming steel with oxidation resistance for automobiles according
to claim 1, wherein a microstructure of the hot-forming steel includes a ferrite,
a martensite and a retained austenite.
3. The high-plasticity hot-forming steel with oxidation resistance for automobiles according
to claim 2, wherein the ferrite has a volume fraction of 5%-12%, the martensite has
a volume fraction of 78%-89%, and the retained austenite has a volume fraction of
6%-10%.
4. The high-plasticity hot-forming steel with oxidation resistance for automobiles according
to claim 1, wherein a tensile strength of the hot-forming steel is 1400MPa-1700MPa.
5. The high-plasticity hot-forming steel with oxidation resistance for automobiles according
to claim 1, wherein an oxidation resistance rate of the hot-forming steel is < 0.1g/(m2·h).
6. The high-plasticity hot-forming steel with oxidation resistance for automobiles according
to claim 1, wherein a yield strength of the hot-forming steel is 900MPa-1450MPa.
7. The high-plasticity hot-forming steel with oxidation resistance for automobiles according
to claim 1, wherein an elongation of the hot-forming steel is ≤18.0%.
8. The high-plasticity hot-forming steel with oxidation resistance for automobiles according
to claim 1, wherein a surface of the hot-forming steel is not completely decarburized
with a thickness of decarburized layer ≥15 µm.
9. The high-plasticity hot-forming steel with oxidation resistance for automobiles according
to claim 1, wherein the thickness of the hot-forming steel is 0.8mm-12.0mm;
10. A hot-forming process of the high-plasticity hot-forming steel with oxidation resistance
for automobiles, comprising following steps:
(1) placing a hot-forming substrate containing the compositions according to any one
of claims 1 to 9 into a heating furnace at a temperature of AC3-AC3+15°C for heating and heat preservation for a period of 180s-300s; and
(2) taking the heated hot-forming steel out of the heating furnace for air cooling
to a temperature of Ar3 and staying for 5s-8s before being put into a hot-forming mold for deformation and
cooling, at a cooling rate of ≤18°C/s, performing the pressure holding for 40s-80s
after cooling to 180°C-250°C, and taking out the formed parts for air cooling to room
temperature after pressure holding to obtain the hot-forming steel.