Object of the Invention
[0001] The present invention relates to a high-strength and high-quench hardenability leaf
spring steel, with a long fatigue life, which can be applied in the iron and steel
industry, which allows being used for metal structures in the construction sector.
Said parts are particularly suitable in the automotive industry, for example, for
manufacturing leaf springs or other suspension supporting elements for industrial
vehicle suspension systems.
[0002] The invention allows obtaining leaf spring steel, from a chemical composition and
by means of a metallurgical process, that has high mechanical strength while at the
same time it has a long fatigue life and strength, in addition to having optimal quench
hardenability.
Background of the Invention
[0003] The main feature of leaf spring steels is their elastic behavior, such that they
become deformed in response to an external stress and recover their original shape
when that stress disappears.
[0004] One of the applications of spring steels are suspension elements, particularly springs,
leaf springs and other elements and devices used in automotive vehicles, railway vehicles
and industry. In this field, leaf spring steels must have very high tensile strength
and yield strength values to assure the elastic behavior of the element. Furthermore,
these properties must be maintained over time, preventing permanent plastic deformations
from occurring.
[0005] These features are largely determined by the carbon content in the steel, which ranges
between 0.40% and 0.65% by weight, as well as the content of other alloy elements
such as Si, Mn, Cr, Ni, Mo and V, for example, the purpose of which is to increase
the quench hardenability of the steel and assure that the microstructure of the quench
hardened part is martensite throughout the entire section.
[0006] Furthermore, other requirements for leaf spring steels is that they have to have
a good fatigue response, considering the cyclical service demands of suspension elements;
good corrosion resistance given that, due to the location thereof in the vehicle and
despite incorporating paint or other anticorrosion protection, they are exposed to
atmospheric inclemencies and/or to impacts that degrade their protective layer; low
hydrogen embrittlement sensitivity, which accelerates the progression of small cracks,
and moderate toughness at room temperature and at a low temperature, given that they
can be used in environments with sub-zero temperatures.
[0007] There are a number of leaf spring and spring steels classified as such in international
standards which have a tensile strength ranging between 1300 MPa and 2000 MPa. These
values, however, depend considerably on the thickness of the part and the highest
values are only obtained in springs that are not very thick, in general coil springs
manufactured from cold and hot formed wire rod.
[0008] For very thick suspension elements, such as leaf springs used in industrial vehicles,
very high-quench hardenability steels are required, the most common steel grades being
55Cr3, 51CrV4 or 52CrMoV4 and rounded rectangular section.
[0009] Leaf spring steels are hot formed at a temperature between 950°C and 1150°C, after
a heating process that can be from gas combustion, induction and other means and that
usually is done in the presence of an oxidizing atmosphere for a more or less prolonged
time, for example between 30-75 minutes for each end. These processes deteriorate
the steel surface either due to decarburization, surface scale formation, which negatively
affects the fatigue behavior of the part.
[0010] In the case of coil springs, said time is substantially less, so the problem of decarburization,
unlike the case of leaf spring steels, is not so relevant.
[0011] In addition to the aforementioned, there are steels and methods for obtaining them
today that are aimed at improving the service features of steels intended for the
applications discussed above, in which variable amounts of alloying elements, such
as Si, Mn, Cr, Ni, Mo, Cu, V, Ti, Al, Nb or B, for example, are usually added, examples
of which are mentioned below.
[0012] Patent no.
WO-2011/074600-A1 describes a method for obtaining steel for leaf springs with a Ti alloy and Ti/N
ratio ≥10 which prevents bainite from occurring and, with it and a hot shot peening
treatment of the component, improves the fatigue life for leaf springs with a Vickers
hardness greater than 510 HV.
[0013] On the other hand, Japanese patent application no.
JPH-08295984-A describes a steel with a low Mn content for leaf springs with high toughness and
delayed fracture strength for tensile strengths of 1650 MPa.
[0014] Chinese patent application no.
CN-102586687-A describes a leaf spring steel with a strength of up to 1750 MPa and high-quench hardenability,
but having reduced ductility even for tempering treatment at 500°C.
[0015] Other high-strength steel inventions relate to applications of wire rod of small
thickness for coil suspensions such as those referred to below as an example.
[0016] Chinese patent no.
CN-102634735-A describes a high-strength alloy steel, with an addition of Cu between 0.50% and 0.80%
and of rare earth elements between 0.02% and 0.07%, reaching a mechanical strength
≥2000 MPa for springs having a diameter <16 mm.
[0017] Patent no.
WO-2012/063620-A1 relates to the invention of an Si-Mn spring steel having high corrosion resistance
to be applied to cold- or hot-formed coil springs, as well as to the high-strength
spring manufactured from this steel.
[0018] Patent no.
WO-2010/110041-A1 solves the problem of the lack of ductility of high-strength steels by means of austempering
an Si-Mn-Cr steel which generates a high-strength mixed bainite and retained austenite
microstructure having good ductility.
[0019] Patent no.
WO-2008/102573-A1 improves the toughness of high-strength steel by means of adding high Si and a suitable
balance of tempering temperatures and times preventing the transformation of ε carbides
into cementite.
[0020] The improvement of corrosion fatigue strength of the high-strength steels is solved
in patent no.
WO-2006/022009-A1 by means of adding anti-corrosive elements such as Cu and Ni, the improvement of
the deoxidation process which drastically reduces the content of oxides having a size
greater than 10 µm in diameter and a suitable balance of other alloy elements (Si,
Mn, Cr).
[0021] The improvement of toughness in high-strength steels is obtained in patent no.
WO-1998/051834-A1 by means of refining grain by the microprecipitation effect and decreasing impurities
at austenite grain boundaries, with a suitable balance of alloy elements (Si, Ti,
B).
[0022] The increase in tensile strength above 2000 MPa and in fatigue strength of steels
for coil springs is obtained in the Japanese patents
JP 2842579-B2 and
JP 3255296-B2 by means of a suitable balance of alloy elements (Si, Ni, Cr, Mo, V) and by restricting,
in number and size, the content of oxides in the steel.
[0023] The weight reduction of suspension arms and leaf springs in industrial vehicles requires
high mechanical strength (≥1800 MPa) steels in parts that are between 10 and 60 mm
thick and between 50 and 150 mm wide, with a long fatigue life, good corrosion resistance
and corrosion fatigue strength, low hydrogen embrittlement susceptibility and moderate
toughness and impact resistance at low temperatures. This challenge has still not
been solved in its entirety by the state of the art.
[0024] Therefore, the properties of the parts manufactured with spring steels intended for
said applications are susceptible to optimization.
Description of the Invention
[0025] The present invention relates to a leaf spring steel, in which an optimal combination
of two opposing mechanical properties, high tensile strength, with strength values
of at least 1800 MPa, and high ductility, with elongation values >9% and area reduction
values >30%, has been obtained as a result of several investigations.
[0026] The invention allows obtaining leaf spring steel from a novel chemical composition
and a specific metallurgical process, having optimized and adjusted resistance to
decarburization, high mechanical strength while at the same time having good ductility,
in addition to having optimal quench hardenability, which is important, for example,
for the complete transformation of austenite into martensite in very thick parts.
[0027] On the other hand, in addition to the chemical composition, the heat treatment applied
to the steel has a very important effect on the mechanical features of the end component,
i.e., the part with the initial chemical composition is subjected to a specific method
of quench hardening and tempering, which must be performed under specific time and
temperature conditions.
[0028] To assure a long fatigue life it is necessary to apply during the process of manufacturing
this steel a specific inclusion deoxidizing and floating method under certain special
conditions.
[0029] The inventors have found a synergistic effect between a novel combination of chemical
elements and a method for obtaining said steel which contemplates a specific heat
treatment, achieving a high strength and ductility leaf spring steel for quench hardening
and tempering, in addition to good hot forming ability and good quench hardenability.
[0030] The investigations resulted in a new grade of SiCrMoV alloy steel, comprising the
following chemical composition by weight percentage:
0.45% ≤ C ≤ 0.58%
0.75% ≤ Si ≤ 2.25%
0.65% ≤ Mn ≤ 1.20%
0.65% ≤ Cr ≤ 1.50%
0.01% ≤ Mo ≤ 0.40%
0.01% ≤ V ≤ 0.40%
the remaining elements being impurities resulting from the production thereof.
[0031] These alloy elements are used in alloy steels to improve tensile strength, tempering
resistance, toughness or other characteristics, but not with the concentrations by
weight indicated, not with the proposed combination of elements, or for obtaining
the properties described above which allow use thereof in the mentioned applications.
[0032] Each of the alloy elements, in the proportions indicated above affects specific parameters
and properties of the steel that is finally obtained.
[0033] Carbon is an indispensable element for obtaining high strength and hardness after
the quench hardening and tempering treatment. Below 0.45% carbon, the strength that
is obtained is insufficient. On the other hand, above 0.58%, the toughness of the
steel markedly decreases and hydrogen embrittlement may be favored. The optimal range
is between 0.47% and 0.55%
[0034] Silicon is one of the most important hardeners of ferrite by solid solution. Given
that it dissolves in ferrite and not in cementite, it tends to inhibit carbide precipitation,
and therefore shifts the temperature of the tempering brittleness area to higher temperatures,
preventing hydrogen embrittlement and improving corrosion fatigue strength. Furthermore,
silicon is a powerful deoxidizer and is used as such in refining processes in iron
and steel processes. Likewise it increases quench hardenability and hardens the ferrite
matrix of the martensite substituting the iron atoms of the lattice. In order for
these effects to translate into a significant increase in strength of at least 0.75%
silicon is required, recommending for this application a silicon content over 0.90%
However, excessive silicon content favors decarburization and the intergranular oxidation
given its tendency to combine itself with the oxygen from the atmosphere at the forging
or rolling temperatures (>1000°C). Furthermore, silicon contributes to shifting the
ductile-fragile transition temperature to higher temperatures, such that if the silicon
content is very high, the steel can be embrittled to room temperature, such that the
upper limit is established at 2.25% to assure an acceptable toughness, 2.00% to assure
an acceptable decarburization in quench hardening and tempering treatments and 1.75%
to assure acceptable decarburization in rolling and re-rolling process of the leaf
spring, depending on the process used. In the case of heating by a gas oven, silicon
tends to combine with O
2 and greater decarburization takes place, whereby it would need to be limited to 1.75%
or even 1.50%. In the case of heating by induction, decarburization is lower and the
upper limit can be left at 2.00%. Silicon improves the mechanical properties of the
steel.
[0035] Manganese is an indispensable element for assuring the required quench hardenability
in steel for leaf springs. Furthermore, it reduces the transformation temperature,
which allows obtaining a fine-grain crystalline structure, which at the same time
allows increasing strength and improving toughness. It also prevents the harmful effect
of the sulfur, combining with said sulfur to form MnS. On the other hand, an excessive
content can favor the occurrence of quench hardening cracks, such that the optimal
content is between 0.65% and 1.20%, even being able to be limited between 0.80-1.10%.
[0036] Chromium is an indispensable element for assuring the required quench hardenability
in steel for leaf springs. If it is below 0.65%, the quench hardenability may not
be enough and unwanted structures may occur in the core of the part. A high chromium
content increases the risk of quench hardening cracks. Chromium carbides also act
like local electrodes on the surface of the steel by increasing pitting corrosion
and reducing the corrosion fatigue strength. The upper limit is therefore established
at 1.50%. The best combination of properties is obtained for a range consisting of
0.80% to 1.25%Cr.
[0037] Molybdenum has a strong, quench hardenability-favoring effect, in turn being a strong
carbide-forming element, providing a notable effect of secondary hardening during
tempering. On the other hand, molybdenum improves pitting corrosion resistance and
prevents tempering brittleness by preventing phosphorus precipitation at the grain
boundary. Nevertheless, in high contents, the alloy cost is excessive and economically
unacceptable, such that the preferred range is between 0.01% and 0.40%. The best ratio
between cost and characteristic is obtained between 0.10% and 0.30% of molybdenum.
[0038] Vanadium is a microalloying element that contributes to refining grain size and causes
intense precipitation hardening, and it greatly increases quench hardenability when
it remains in solid solution. Vanadium precipitates are hydrogen nucleators, such
that they fix the hydrogen in corrosive environments and improve the delayed fracture
strength induced by hydrogen. However, with a very high vanadium content, precipitates
coalesce and their effect can become harmful. Therefore, the vanadium content must
be between 0.01% and 0.40%, a content between 0.05% and 0.30% being preferable.
[0039] Furthermore, the steel proposed by the invention may comprise, in addition, at least
one of the following elements or a combination thereof, with a weight percentage:
P ≤ 0.040%
S ≤ 0.040%
Cu ≤ 0.50%
0.001% ≤ Al ≤ 0.050%
0.001% ≤ Nb ≤ 0.100%
0.001% ≤ Ti ≤ 0.050%
0.004% ≤ N ≤ 0.020%
the remaining elements being residual elements that result from obtaining the steel.
[0040] Phosphorus hardens steel and segregates at austenite grain boundaries, drastically
reducing the toughness of the steel. Furthermore, it favors hydrogen embrittlement
and delayed fracture. The phosphorus content is limited to less than 0.040% in order
to limit its adverse effect, a content less than 0.020% being desirable.
[0041] Sulfur embrittles steel in a manner similar to phosphorus. Despite this effect being
counteracted by combining with manganese, manganese sulfides form inclusions that
deform longitudinally in the forging or rolling direction and considerably deteriorate
the transverse mechanical properties and the fatigue behavior. Nevertheless, sometimes
a minimum amount of sulfur is required to improve the machinability of the steel and
the forming thereof by machining. Therefore, the sulfur content is restricted to less
than 0.040%, a content less than 0.015% being preferable.
[0042] Adding copper prevents decarburization of steel and improves corrosion resistance
in a manner similar to nickel by inhibiting the growth of corrosion-induced pitting.
However, a high copper content impairs hot ductility of steel, such that the upper
limit of copper is established at 0.50%. For optimal hot processing, the maximum copper
content must be limited to 0.30%.
[0043] Aluminum is an element that acts as a powerful deoxidizer during the steel manufacturing
process. Aluminum forms aluminum nitrides which contribute to controlling the austenitic
grain size during heat treatments and heating prior to hot forming processes. Nevertheless,
it forms very hard oxides which are very prejudicial for fatigue life, such that the
upper limit thereof is established at less than 0.050%.
[0044] Niobium is a microalloying element having effects that are similar to those of vanadium
in controlling grain size and in precipitation-induced hardening of steel, such that
it contributes to increasing mechanical strength and to improving toughness. Furthermore,
niobium precipitates fix the hydrogen attacking the steel in corrosive environments,
improving delayed fracture strength. Content above 0.100%, nevertheless, causes coarsening
of the precipitates, which is prejudicial for the mechanical properties. The optimal
niobium content is established between 0.001% and 0.100%.
[0045] The titanium is an effective austenitic grain size controller at a high temperature,
typically at hot forging temperatures. However, given its affinity for nitrogen, it
forms titanium nitrides at temperatures close to those of liquid steel, which transforms
its precipitates into extremely hard inclusions that are harmful for fatigue life.
The titanium content in the steel is limited to a maximum of 0.050% to limit excessive
titanium nitride coarsening.
[0046] Nitrogen combines with Ti, Nb, Al and V to form nitrides, the precipitation temperatures
of which depend on the respective content of the different elements and on constant
characteristics. With a suitable size, those nitrides exert a pinning effect on the
austenitic grain, controlling its size at high temperature and preventing the coalescence
and growth thereof. However, if the nitrogen content or the microalloying element
content is very high, precipitation occurs at a high temperature, and the precipitates
become coarse, becoming ineffective for controlling the grain and prejudicial for
fatigue life. Therefore, the nitrogen content in the steel is limited to 0.004% to
0.020%.
[0047] It has previously been found that spring steels having a standard composition and
process for truck leaf spring applications which have been subjected to a conventional
quench hardening and tempering process did not come to have the required and previously
discussed mechanical properties due to fact that the degree of inclusion cleanliness
was lower and the balance of microalloying elements was inadequate with respect to
the optimized process that the steel of the invention has.
[0048] A preferred composition of the steel proposed by the invention comprises a weight
percentage:
0.47% ≤ C ≤ 0.55%
0.90% ≤ Si ≤ 2.00%
0.75% ≤ Mn ≤ 1.20%
0.80% ≤ Cr ≤ 1.25%
0.10% ≤ Mo ≤ 0.30%
0.05% ≤ V ≤ 0.30%.
[0049] For this preferred composition, the steel can additionally comprise at least one
of the following elements, or a combination thereof, by weight:
P ≤ 0.020%
S ≤ 0.015%
Cu ≤ 0.50%
0.001 % ≤ Al ≤ 0.050%
0.001 % ≤ Nb ≤ 0.060%
0.001 % ≤ Ti ≤ 0.030%
0.004% ≤ N ≤ 0.020%.
[0050] Therefore, after various experiments a rigorous method has been developed for obtaining
steel according to the following steps:
- Rigorously controlling the raw materials of the furnace, i.e., coke and lime and especially
scrap.
- Using between 30% and 50% top-quality scrap.
- Performing an oxidizing period in an electric furnace, which is important for dephosphorization
of the steel, prior to the foamed slag.
- Once the foamed slag has ended, deslagging until virtually leaving the furnace with
no slag, the objective being a presence of phosphorus in this step less than 0.010%
by weight.
- Tilting with standard temperature and parts per million (ppm) of oxygen, according
to a clean steel standard, assuring that slag does not pass from the furnace to the
ladle.
- Deoxidizing with Si to obtain very fluid white slag with a lime-spar base.
- Rigorously controlling the refining raw materials, i.e., ferroalloys and other metallic
and slag forming additions.
- Establishing a prolonged vacuum, considering as a vacuum time that which is below
1 mbar, and being 50% greater than the conventional vacuum time.
- Ending the vacuum treatment with a high enough temperature to perform an inclusion
decanting process after said process of at least fifteen minutes, without performing
any type of addition or heating.
- Finally, a meticulous casting process with special protection for the liquid steel
stream must be followed.
- If the solidification process is during continuous casting, casting, cooling and stirring
speed conditions will be adjusted to obtain a homogenously solidified microstructure.
[0051] This entire method of manufacturing steel allows achieving low sulfur levels, below
0.015% by weight, and low phosphorus levels, below 0.020% by weight, in addition to
a low inclusion level.
[0052] CCT (Continuous Cooling Transformation) diagrams allow representing heat treatments
for a certain chemical composition when the phase transformations occur in non-equilibrium
conditions.
[0053] The solidification products are subsequently transformed when hot by means of a process
consisting of heating at a temperature greater than 1100°C and a series of consecutive
deformations by means of hot forging or rolling until obtaining an intermediate product
having the suitable section, shape and microstructure.
[0054] After various experimental tests, it has been verified that after the process of
manufacturing steel proposed by the invention, with the chemical composition indicated
above, adjusting the temperatures and the maintenance times of the quench hardening
and tempering, a steel with tensile strength above 1800 MPa and high ductility, with
reduction of area >30%, is obtained. Furthermore, said steel has high-quench hardenability,
which is suitable for obtaining 100% martensite in thick sections, such as those of
leaf springs for industrial vehicles.
[0055] To obtain a part of the previously obtained steel having the mentioned features,
the invention contemplates performing a method whereby said part of steel is obtainable.
[0056] The method for obtaining parts of said steel comprises a hot forming process, with
prior heating at a temperature greater than 950°C which allows providing the steel
with sufficient ductility when hot, to confer to the part of steel a shape similar
to that of the end component. After being shaped, the part is left to be air cooled.
[0057] The method subsequently contemplates a quench hardening process which is performed
with austenization at a temperature greater than 800°C, followed by final forming
operations and then subsequent cooling, for example, in oil. The steel of the invention
has a balance of alloy elements that allows obtaining 100% martensite, even in the
thicker sections, without increasing the risk of cracks resulting from quench hardening
appearing due to the stress produced during cooling.
[0058] The method then comprises a tempering process, which is carried out at a temperature
greater than 300°C for at least one hour, thus achieving the adjustment of the hardness
and toughness of the material, in addition to preventing decreases in resilience,
which are associated with the brittleness phenomenon of tempering.
[0059] Finally, the method comprises carrying out a shot peening process by applying or
not applying stress to the component at a temperature between 0°C and 400°C, usually
at room temperature, to generate in surface regions of the component residual compressive
stresses improving its fatigue behavior. A surface coating or painting that improves
the corrosion behavior of the component can additionally be applied.
[0060] Therefore, the method for obtaining parts of steel comprises the following steps:
- Obtaining the previously described steel of the invention, in which the selected steel
comprises the previously defined general composition or preferred composition
- Manufacturing a part of said steel, for example by means of rolling or another forming
process.
- Performing the previously defined quench hardening treatment in the part.
- Performing the previously defined tempering treatment in the part.
- Performing a shot peening treatment in the part.
- Painting or coating the part with an anticorrosion treatment.
Description of the Drawings
[0061] To complement the description that is being made and for the purpose of aiding to
better understand the features of the invention according to a preferred practical
embodiment thereof, a set of drawings is attached as an integral part of said description
in which the following is depicted with an illustrative and non-limiting manner:
Figure 1 shows a Jominy quench hardenability curve diagram obtained for each of the
steels A-H. Steels C, D and H show virtually flat curves, whereas drops in hardness
occur in steels A, B, E, F and G at distances from the quench hardened end equal to
or less than 40 mm.
Figures 2-4 show the microscopy of the surface of steels B, H and A, respectively,
after heating at 960°C for 110 minutes.
Figures 5-7 show the microscopy in which the decarburized layer of the same steels
B, H, and A after heating at 1030°C for 35 minutes, followed by heating at 960°C for
45 minutes.
Embodiments of the Invention
Example 1
[0062] The tests performed with steel specimens with other compositions different from the
chemical composition of the steel of the invention are described below by way of example.
Said specimens are steels A-G, steel H is the steel of the invention. Table 1 shows
the chemical compositions by weight percentage, the rest being Fe and impurities:
Table 1
| |
C |
Mn |
Si |
P |
S |
Cr |
Ni |
Mo |
V |
Cu |
Al |
N |
| A |
.55 |
.79 |
1.94 |
.008 |
.013 |
.95 |
.14 |
.004 |
.12 |
.15 |
.005 |
.0092 |
| B |
.50 |
.78 |
.28 |
.009 |
.013 |
1.03 |
.15 |
.18 |
.12 |
.15 |
.007 |
.0144 |
| C |
.55 |
.79 |
.34 |
.011 |
.004 |
1.03 |
1.60 |
.003 |
.12 |
.15 |
.008 |
.0131 |
| D |
.50 |
.79 |
.99 |
.013 |
.004 |
.96 |
.15 |
.18 |
.003 |
.15 |
.008 |
.0082 |
| E |
.51 |
.78 |
.31 |
.013 |
.003 |
1.05 |
.15 |
.003 |
.12 |
.15 |
.009 |
.0083 |
| F |
.53 |
.84 |
1.04 |
.013 |
.003 |
1.12 |
.15 |
.003 |
.13 |
.16 |
.011 |
.0091 |
| G |
.52 |
.80 |
.33 |
.013 |
.003 |
1.07 |
.15 |
.004 |
.26 |
.15 |
.005 |
.0089 |
| H |
.50 |
.79 |
1.02 |
.012 |
.003 |
1.07 |
.14 |
.18 |
.12 |
.15 |
.007 |
.0080 |
[0063] Table 2 includes the ideal critical diameter values according to data tabulated in
the ASTM A255-02 standard for each of the compositions and steels described in Table
1.
Table 2
| |
A |
B |
C |
D |
E |
F |
G |
H |
| Dl (mm) |
227 |
175 |
191 |
197 |
120 |
193 |
155 |
259 |
[0064] Illustration 1 shows the Jominy quench hardenability curve diagram obtained for each
of steels A-H. Steels C, D and H show virtually flat curves, whereas drops in hardness
occur in steels A, B, E, F and G at distances from the quench hardened end equal to
or less than 40 mm. [/*/*]

[0065] All these steels were subjected to quench hardening and tempering treatments under
different conditions for the purpose of achieving for each of them the most optimal
mechanical strength and toughness combination.
[0066] Therefore, the mechanical strength for each steel and each tempering temperature
is shown in Table 3.
Table 3
| |
Strength (MPa) vs. Tempering Temperature |
| |
300°C |
350°C |
400°C |
450°C |
| A |
2075 |
2099 |
1938 |
1736 |
| B |
1932 |
1845 |
1695 |
1554 |
| C |
1965 |
1796 |
1650 |
1500 |
| D |
2144 |
1992 |
1838 |
1656 |
| E |
1653 |
1615 |
1536 |
1319 |
| F |
2138 |
2046 |
1814 |
1658 |
| G |
1731 |
1569 |
1562 |
1352 |
| H |
2050 |
2028 |
1874 |
1691 |
[0067] The reduction of area results for each steel and temperature are shown in Table 4.
Table 4
| |
Reduction of Area (%) vs. Tempering Temperature |
| |
300°C |
350°C |
400°C |
450°C |
| A |
13 |
14 |
14 |
15 |
| B |
25 |
19 |
27 |
32 |
| C |
20 |
4 |
33 |
30 |
| D |
- |
6 |
11 |
15 |
| E |
11 |
26 |
19 |
32 |
| F |
19 |
7 |
22 |
36 |
| G |
34 |
41 |
41 |
47 |
| H |
10 |
11 |
33 |
38 |
[0068] As shown in Tables 3 and 4, steels A, B, C, D, E, F and G do not attain strength
of 1800 MPa, maintaining a minimum area reduction ≥30%.
[0069] Steels B, C and E have low silicon contents, such that they do not attain 2000 MPa
for any tempering temperature.
[0070] In turn, steels A, D and F do not achieve desired ductility levels despite having
a high silicon content and exceeding 1800 MPa for tempering temperatures equal to
or less than 400°C, because the alloying element combination is not the suitable combination
for attaining the required mechanical features.
[0071] However, for steel H, which has a chemical composition within the limits object of
the invention, i.e., it is the steel proposed by the invention, it has been found
that after being subjected to a quench hardening and tempering treatment, consisting
of quench hardening plus tempering, said steel attains the required mechanical features
and its quench hardenability is high.
[0072] Furthermore, the steel of the invention has a moderate decarburization similar to
steels commonly used in leaf spring, which allows the processing thereof by hot forming
without deteriorating the surface quality of the steel bar.
[0073] Figures 2, 3 and 4 show the surface of steels B, H and A, respectively, after heating
at 960°C for 110 minutes. The steel A, with 1.94% Si, shows total surface decarburization,
which is unacceptable for a leaf spring application given the lower resistance of
the area subjected to greater stress in service.
[0074] Figures 5, 6 and 7 show the decarburized layer of the same steels B, H and A after
heating at 1030°C for 35 minutes, followed up by heating at 960°C for 45 minutes.
The first treatment is similar to the heating prior to the re-rolling of the leaf
spring and the second treatment is similar to the austenization process prior to quench
hardening.
[0075] Steel A, with 1.94% Si, as can be seen in Figure 7, shows a very thick decarburized
layer (0.20-0.25 mm) that negatively influences the performances of the part. Steels
B and H, with 0.28% Si and 1.02% Si, respectively, depicted in Figures 5 and 6, show
much less partial decarburization and total decarburization is not observed.
[0076] Steel H, located within the limits of the invention, has the quench hardening necessary
to assure 100% martensite in thick sections, without generating excessive stress during
quench hardening giving rise to cracks. Likewise, it acquires a resistance of 1800
MPa through thermal quench hardening and tempering treatment, maintaining a minimal
area reduction ≥30%. All this by maintaining a resistance to decarburization that
is sufficient so as not to lose surface mechanical properties.
[0077] The invention is described according to some preferred embodiments thereof, but for
the person skilled in the art it will be obvious that multiple variations can be introduced
in said preferred embodiments without exceeding the object of the claimed invention.