[0001] The invention relates to high strength steel with increased E-modulus and to a method
for producing said steel.
[0002] In the automotive industry, where lighter vehicles and safety are of constant concern,
steel with a higher E-modulus allows the use of thinner gauge parts which still have
the stiffness and strength of thicker and thus heavier parts. Also in other types
of applications such as in yellow goods, aerospace or construction the combination
of high E-modulus and high strength is an interesting combination of properties. A
known way to increase the modulus of elasticity and reduce the weight of steel is
by incorporating ceramic particles of different natures, such as carbides, nitrides,
oxides or borides. These particles have a much higher elastic modulus, ranging from
about 300 to 550 GPa, than that of the steel base which has an E-modulus around 205-210
GPa. One way of including ceramic particles uniformly distributed in a matrix of steel
is by means of powder metallurgy.
[0003] Despite improved mechanical properties in comparison with conventional steels containing
no dispersion of ceramic particles, this type of method like powder metallurgy has
problems. Reactions of the metal powders are difficult to prevent because of the high
surface area of the metal powders. Even after compacting and sintering, there may
be residual porosity that may play a role in inducing fracture during cyclic loading.
Uniform distribution of the particles in the matrix is difficult to achieve. Moreover
the chemical composition of interfaces matrix/particle, and therefore their cohesion
is difficult to control because of the surface contamination of the powders before
sintering. In addition, the cost of the process like power metallurgy is very high.
This type of process is therefore potentially suitable for production in small quantities
but not for economic production on the scale required for the automotive and construction
industry.
[0004] In
EP1897963 steel is proposed based on the formation of large quantities of titaniumdiboride
particles (TiB
2). It describes steel comprising 2.5 to 7.5% titanium and about 0.8 to about 4% boron.
The result of these additions is that large numbers of eutectic TiB
2-precipitates are formed in the steel matrix and these particles leads to increase
of the E-modulus and decrease of the density of the steel. A disadvantage of this
steel type is that it is very difficult to produce the TiB
2-precipitates as fine eutectic precipitates. Because of addition of large amount of
Ti, the cost of this type steel is quite high. A similar solution is chosen in
JP2007-051341 where the mandatory presence of large amounts of titanium and vanadium is complemented
by a mandatory presence of large amounts of chromium to produce and stabilise the
formation of V
3B
4 making the costs of the alloy very high.
[0005] It is an object of this invention to provide a steel product with a higher E-modulus
than conventional steels.
[0006] It is also an object of this invention to provide a steel product that is much more
economic than steel with TiB
2 or vanadium containing borides
[0007] It is also an object of this invention to provide a method of mass producing the
steel product of the invention in an economical way.
[0008] One or more of these objects are reached by a steel comprising in wt. %
• 0.001 ≤ C < 0.3
• 1.0 ≤ B < 3.0
• 0.05 ≤ Mn < 3.0
• 0.0 ≤ Cr < 2.0
• 0.0 ≤ Si < 1.0
• 0.005 ≤ Al_sol < 0.5
• 0 ≤ S < 0.030
• 0 ≤ P < 0.10
• 0 ≤ Ni < 1.0
• 0 ≤ Cu < 1.0
• 0 ≤ Mo < 0.4
• 0.0 ≤ Ti < 2.5
• 0.0 ≤ Nb < 0.2
• 0.0 ≤ V <0.2
• 0.0 ≤ N < 0.04
• balance iron and unavoidable impurities resulting from production,
wherein the steel comprises at least 10 wt% of Fe
2B-particles.
[0009] All compositional percentages are in weight percent (wt.%) unless otherwise indicated.
The unavoidable impurities are elements unavoidably contained in the steel due to
circumstances such as raw materials, manufacturing facilities, etc.
[0010] Carbon is added to increase the strength of steel matrix.
[0011] Boron is an important element for forming Fe
2B. Fe
2B-particles raise the E-modulus of the steel. Below the lower end of the inventive
range the contribution of the precipitates to the increase of the E-modulus is insufficient.
On the other hand, if the content exceeds 3.0% the volume fraction of borides is too
high which has a negative impact on ductility and workability.
[0012] Manganese contributes to the strengthening of the matrix by solid solution and increasing quenching-hardening-ability
of steels. Manganese is also effective in binding sulphur thereby reducing the risk
of hot-cracking during hot rolling. However the amount of Mn above 3% increases the
risk of segregation and band formation to an unacceptable level. A suitable minimum
manganese content is 0.05%.
[0013] Chromium is an element effective in increasing quenching-hardening-ability of steel and the
strength of the matrix. Too high Cr increases the cost of steel and an excessive addition
of Cr leads to precipitate (Fe, Cr)-borides which is not desirable in the context
of this invention. The chromium content is therefore preferably below 2%. When present
as an alloying element then a suitable minimum amount is 0.05% and preferably 0.1%.
[0014] Aluminium is added mainly for deoxidation. An amount of about or higher 0.005% is effective
in the deoxidation of the melt. On the other hand, high Al-contents result in deterioration
in ductility and castability due to the formation of harmful coarse alumina inclusions.
Therefore the maximum content should not exceed 0.5%. The aluminium content in the
steel is expressed as Al-sol (acid soluble), meaning that the aluminium is not bound
to oxygen. The killing of the steel during steelmaking requires the addition of a
deoxidant, usually aluminium and sometimes silicon, to bind the oxygen into alumina.
[0015] Silicon is an element increasing strength of steel. However, a Si-content of more than 1%
will negatively affect surface quality of steel and galvanisability of steel products.
Therefore the Si-content should be preferably below 1.0%.
[0016] Nitrogen is an impurity element that consumes Ti to form TiN and should be kept as low as
possible. Although the maximum allowable nitrogen content is 0.040% (400 ppm), the
nitrogen should preferably be controlled below 0.020%.
[0017] If
Sulphur is added in amounts exceeding 0.030%, then the risk of MnS formation becomes too
great. MnS is known to adversely affect hot and cold formability.
[0018] Phosphorus segregates at the grain boundaries. To maintain sufficient hot ductility and avoid
hot-cracking during solidification and welding the amount should not exceed 0.10%.
[0019] Niobium and Vanadium form boride with B that is beneficial to the E-modulus. The amount of
Nb and V should be limited to 0.2% due to their very high cost.
[0020] Titanium forms TiB2 with B that is beneficial to a high E-modulus. However, Ti should be limited
to 2.5% due to its high cost.
[0021] Optionally,
nickel, copper and
molybdenum can be added which increase the strength of and quenching-hardening-ability of the
steel matrix. For economic reasons, the additions should be limited to 1%, 1% and
0.4% by weight respectively.
[0022] In an embodiment the E-modulus of the steel is at least 225 GPa, preferably at least
230 GPa.
[0023] In an embodiment the structure of the steel comprises at least 12 wt.% of Fe
2B, more preferably at least 15 wt.%.
[0024] In an embodiment of the invention the boron content is at least 1.5% and/or at most
2.5 wt.%.
[0025] In an embodiment the precipitates have an average size of below 10 µm. preferably
the average size is below 3 µm.
[0026] According to a second aspect, a method is provided for producing the steel as claimed
in any one of claims 1 to 4. A big advantage is that according to this method the
steel according to the invention can be mass produced using conventional steel producing
equipment without the need to use powder metallurgy as a production method. Preferably
the steel melt from which the steel according to the invention is made by using Ferro-alloys.
The steel melt or steel is not produced by powder metallurgy. This makes the steel
much easier to produce in mass, and thereby more economically.
[0027] The advised temperature range for reheating is between about 0.8 and 0.95*Tm, Tm=melting
temperature in °C. In view of the low melting point of the steel, which may be below
1150°C, depending on the composition, reheating for hot rolling has to be controlled
to be below 0.95*Tm. The steel preferably is hot rolled above the Ar
3r-temperature. The hot rolling preferably takes place while the steel is still austenitic
to achieve a homogeneous structure, although it could be hot rolled in the intercritical
or ferritic region.
[0028] The hot rolled steel may subsequently be subjected to cold rolling to further reduce
the gauge of the material and annealed at the temperature suitable to recrystallise
the grain structure. The steel (cold-rolled or hot-rolled) may also be provided with
a metallic coating to increase its corrosion resistance. This metallic coating preferably
is a zinc or zinc alloy coating, and wherein the coating is applied by electrocoating
or hot-dipping. The alloying elements in the zinc alloy coating may be aluminium,
magnesium or other elements. An example of a suitable coating is the Magizinc
® coating developed by Tata Steel.
[0029] According to a third aspect the steel according to the invention is used in static
constructions such as sections, bridges or bridge parts, buildings, in vehicles such
as cars, yellow goods, trucks, or aerospace applications. In automotive applications
such as vehicles this type of steel can be applied for example in brakes, suspension
components, shock mounts, roof bows, and vehicle floors. In aerospace applications
one of the possible applications are gears and bearings etc., in construction the
structural steels for sections. For yellow goods the possible applications are e.g.
boom and bucket arm structures on backhoes and excavators.
[0030] The invention is now further explained by means of the following, non-limitative
example.
[0031] One 50 kg vacuum furnace melts (under Ar atmosphere) were produced. The melts were
made from very low carbon steel and Ferro-alloys with addition of relevant alloying
elements. The 50 kg melts were cast into two ingots with 100mm x 100mm x 350mm. The
chemical compositions of the casts are given in Table 1.
Table 1. Chemical composition of experimental casts, wt. % unless otherwise specified
(N in ppm) (n.d. = not determined)
| Steel |
C |
Mn |
Al |
B |
| 1 (Tm=1150°C) |
0.066 |
0.19 |
0.07 |
1.9 |
| 2 |
0.066 |
0.19 |
0.07 |
0.005 |
[0032] The microstructure of steel 1 is given in the SEM-micrographs at different magnifications.
[0033] The casts were homogenised at 1100°C for up to 10 hours.
[0034] A slice of 50x100x150 mm was saw off from the ingot and was heated up to 1075°C and
soaked for 45 min and then hot rolled. The hot rolling from 50mm gauge down to 5mm
gauge was performed. Rolling temperature on the surface was higher than 800°C. After
hot rolling, hot rolled plates were coiled at 600°C.
[0035] The percentage of Fe
2B (wt.%) and the E- modulus are given in Table 2.
Table 2. Fe
2B (in wt.%) and E modulus for experimental steels
| Steel |
Fe2B (wt.%) |
E (//RD) (GPa) |
| 1 |
22 |
230 |
| 2 |
<0.1% |
205 |
1. Steel having a chemical composition consisting of
• 0.001 ≤ C < 0.3
• 1.0 ≤ B < 3.0
• 0.05 ≤ Mn < 3.0
• 0.0 ≤ Cr < 2.0
• 0.0 ≤ Si < 1.0
• 0.005 ≤ Al_sol < 0.5
• 0 ≤ S < 0.030
• 0 ≤ P < 0.10
• 0 ≤ Ni < 1.0
• 0 ≤ Cu < 1.0
• 0 ≤ Mo < 0.4
• 0.0 ≤ Ti < 2.5
• 0.0 ≤ Nb < 0.2
• 0.0 ≤ V < 0.2
• 0.0 ≤ N < 0.04
the rest of the composition comprising iron and unavoidable impurities resulting from
production, wherein the steel comprises at least 10 wt% of Fe
2B as particles.
2. Steel according to claim 1 wherein the E-modulus is at least 225GPa, preferably at
least 230GPa.
3. Steel according to any one of claims 1 to 2 wherein the structure of the steel comprises
at least 12 wt% of Fe2B, more preferably at least 15 wt%.
4. Steel according to any one of claims 1 to 3 wherein the particles have an average
size of below 10 µm, preferably below 3 µm.
5. Method for producing the steel of any one of claims 1 to 4 comprising the steps of:
a. providing a steel melt having a composition
• 0.001 ≤ C < 0.3
• 1.0 ≤ B < 3.0
• 0.05 ≤ Mn < 3.0
• 0.0 ≤ Cr < 2.0
• 0.0 ≤ Si < 1.0
• 0.005 ≤ Al < 0.5
• 0 ≤ S < 0.030
• 0 ≤ P < 0.10
• 0 ≤ Ni < 1.0
• 0 ≤ Cu < 1.0
• 0 ≤ Mo < 0.4
• 0.0 ≤ Ti < 2.5
• 0.0 ≤ Nb < 0.2
• 0.0 ≤ V < 0.2
• 0.0 ≤ N < 0.04
b. casting the melt into a suitable starting material for hot rolling by casting an
ingot or bloom or by casting a slab, rod or thin slab, or by casting a strip;
c. heating, reheating or homogenising the ingot, bloom, slab, rod or strip before
hot rolling with a controlled heating rate so as to avoid decohesion between the matrix
and the at least 10 wt% of Fe2B as particles;
d. hot rolling the starting material to the finish hot rolling dimensions.
6. Method according to claim 5 wherein the hot rolling temperature is between 0.5*Tm
and 0.95*Tm.
7. Method according to any of claims 5 to 6 wherein the steel melt is produced by using
Ferro-alloys.
8. Method according to any of claims 5 to 7 wherein the hot rolled steel is subsequently
subjected to cold rolling to further reduce the gauge of the material and annealed
at the temperature suitable to recrystallise the grain structure.
9. Method according to any one of claims 5 to 7 wherein the steel is provided with a
metallic coating to increase corrosion resistance.
10. Method according to claim 9 wherein the metallic coating is a zinc or zinc alloy coating,
and wherein the coating is applied by electrocoating or hot-dipping
11. Steel part produced from the steel according to any one of claim 1 to 4 for use in
static constructions, or in vehicles such as cars, yellow goods, trucks, aerospace
applications or in other engineering applications.