The present invention defines a new class of gray iron alloy, produced by a new method to obtain higher tensile strength, while keeping the machinability conditions compatible with traditional gray iron alloys. More specifically, the material produced by this method can be used either in combustion engines with high compression rates, or in general casts and traditional combustion engines where weight reduction is a target.
Gray iron alloys, known since the end of XIX century, have become an absolute success in the automotive industry due to their outstanding properties, mainly required by combustion engines. Some of these gray iron alloy characteristics have been recognized for a long time as presenting:
However, due to the increasing requirements of combustion engines such as more power, lower fuel consumption and lower emissions for environmental purposes, the traditional gray iron alloys hardly achieve the minimum tensile strength required by combustion engines with higher compression rates. Generally, as a simple reference, such tensile strength requirements start at a minimum 300 MPa, at main bearing location on cylinder blocks or at fire face location on cylinder heads.
Precisely the big limitation of the current gray iron alloys is that they present a drastic decrease of machinability properties when higher tension is required.
Thus, in order to solve such problem, some metallurgists and material experts decided to focus on a different alloy: compact graphite based, usually known as compact graphite iron (CGI). Many papers discuss the CGI properties:
Although the CGI alloy presents outstanding tensile strength, it also presents other serious limitations regarding its properties or industrialization. Among such limitations, we can emphasize:
Lower thermal conductivity;
Lower damping vibration capacity;
Lower machinability level (hence, higher machining costs);
Higher shrink rate (hence, higher tendency for internal porosities); and
Lower microstructure stability (strongly dependent on the cast wall thickness).
In this scenario, the challenge was to create an alloy that keeps the similar outstanding properties of the gray iron alloy, concomitantly with a wide tensile strength interface of the CGI alloy. This is the scope of the present invention.
Currently, the method to obtain a gray iron cast, in the foundries, has the following steps:
Melting Phase: the load (scraps, pig iron, steel, etc) is melted by cupola, induction or arc furnaces.
Chemical Balance: usually performed on the liquid batch inside the induction furnace, in order to adjust the chemical elements (C, Si, Mn, Cu, S, etc) according to the required specification.
Inoculation Phase: commonly carried out at the pouring ladle or at the pouring mold operation (when using pouring furnaces), in order to promote enough nucleus to avoid the undesirable carbide formation.
Pouring Phase: carried out on the molding line at a pouring temperature usually defined in a range to prevent blow holes, burn in sand and shrinkage after the cast solidification. In other words, the pouring temperature is actually defined as a function of the cast material soundness.
Shake-Out Phase: usually performed when the cast temperature, inside the mold, cools comfortably under the eutectoidic temperature (≈700° C.).
Such a process is applied at foundries worldwide and has been the object of many books, papers and technical articles:
Many patent applications reveal compositions with the usual components on gray iron alloys, also applied to the present application. However, comparing to our application, they not present all the components and/or equations that are mandatory to regulate the precise balance between some specifics components in the final composition.
Examples of that is the PCT application WO 2004/083474 of a Volvo composition with the mandatory presence of N in its composition (not applied in our application) or the Japanese application JP 10096040 with the requirement of Ca in its composition (not applied in the present invention). Besides, it is important to inform that the composition of those applications defines ranges of variations in several components that are too wide. If applied in the present invention would deteriorate the main material properties.
Other example is the European Patent EP 0616040 for the desulphurization of a gray cast alloy. In this European application the component “S” must be eliminated. Differently, the present invention requires the “S” component as important factor to generate the necessary nucleus.
The present application will be explained based on the following non limitative figures:
The present invention defines a method to obtain a new alloy, flake graphite based, with the same excellent industrial properties of the traditional gray iron, with higher tensile strength (up to 370 Mpa), which makes this alloy an advantageous alternative if compared with the CGI alloy.
By analytical and practical means, said method can promote an interaction among five metallurgical fundaments: chemical analysis; oxidation level of the liquid batch; nucleation level of the liquid batch; eutectic solidification and eutectoidic solidification. The present method allows the obtainment of the best condition from each one of these fundaments in order to produce this new high performance iron alloy, herein called HPI.
Chemical Analysis
The chemical correction is carried out in traditional ways, at the induction furnace and the chemical elements are the same ones already known by the market: C, Si, Mn, Cu, Sn, Cr, Mo, P and S.
However, the following criteria for the balance of some chemical elements must be kept so that the desirable flake graphite morphology (Type A, size 4 to 7, flakes with no sharp ends), the desirable microstructure matrix (100% pearlitic, max 2% carbides) and the desirable material properties can be obtained:
The carbon equivalent (CE) is defined in the range from 3.6% to 4.0% in weight but, at the same time, keeping the C content from 2.8% to 3.2%. The HPI alloy has a higher hypoeutectic tendency if compared with the traditional gray iron alloys.
The Cr content is defined as max 0.4% and, when associated with Mo, the following criterion must be obeyed: % Cr+% Mo≦0.65%. It will permit the proper pearlitic refinement.
The Cu and Sn must be associated according to the following criterion: 0.010%≦[% Cu/10+% Sn]≦0.021%
The S and Mn contents are defined in specific ranges of the rate % Mn/% S, calculated to guarantee that the equilibrium temperature of the manganese sulfide MnS will always occur under the “liquidus temperature” (preferable near the eutectic starting temperature). Besides improving the mechanical properties of the material, this criterion prompts the nucleus formation inside the liquid batch. Table 1 presents the application of such criterion for a diesel cylinder block where the % Mn was defined between 0.4% and 0.5%.
The Si content range is defined from 2.0% to 2.40%.
The “P” content is defined as: % P≦0.10%.
Oxidation of the Liquid Batch
To obtain the HPI alloy, the liquid batch in the induction furnace must be free of coalesced oxides that do not promote nucleus. Besides, they also must be homogeneous along the liquid batch. So, in order to meet such criterion, a process for deoxidation was developed according to the following steps:
Increase of the furnace temperature over the silicon dioxide (SiO2) equilibrium temperature (TE);
Turning off the furnace power for at least 5 minutes to promote the flotation of the coalesced oxides and other impurities;
Spreading of an agglutinating agent on the surface of the liquid batch; and
Removal of such agglutinant material now saturated with the coalesced oxides, leaving cleaner liquid metal inside the furnace.
Despite the fact that this operation decreases the nucleation level (see
Nucleation of the Liquid Batch
Another important characteristic of the HPI alloy when compared to the traditional gray iron alloys is precisely the elevated eutectic cell number. The HPI alloy presents from 20% to 100% more cells if compared with the same cast performed in current gray iron alloys. This higher cells number directly promotes smaller graphite size and, thus, contributes directly to the increase of the tensile strength of the HPI material. In addition, more cell number also implies more MnS formed in the very core of each nucleus. Such phenomenon is decisive to increase tool life when the HPI material is machined.
After the chemical correction and deoxidation process, the liquid batch inside the furnace must be nucleated according to the following method:
Besides creating new nuclei, said method also increases the active oxides number in the liquid metal inside the furnace.
In sequence, the usual inoculation phase is performed in traditional ways, since long time known by the foundries. However, the difference for HPI alloy is precisely the range of % weight of inoculant applied on the pouring ladle or pouring furnace immediately before the pouring operation: From 0.45% to 0.60%. It represents about twice the % of inoculant currently applied in this step to perform traditional gray iron alloys.
The following step is to specify the nucleation of the liquid metal by thermal analysis. The objective of this application, defines two thermal parameters from the cooling curves as more effective to guarantee a desirable nucleation level:
1) Eutectic Under-Cooling Temperature “TSE” and
2) Range of Eutectic Recalescence Temperature “ΔT”.
Both parameters must be considered together, to define whether the liquid metal is nucleated enough to be compatible with the HPI requirements.
The desirable nucleation of the HPI alloy must present the following values:
TSE: Min 1115° C.; and
ΔT: Max 6° C.
wherein, eutectic temperature undercooling, TSE, is greater than or equal to 1115° C. and range of eutectic recalescence, ΔT, has a maximum of 6° C., wherein TSE and ΔT are two thermal parameters from the cooling curves during nucleation.
As a reference, table 2 below presents the comparison of HPI thermal data using two different inoculants:
As a reference, Table 2 below presents the comparison of HPI thermal data using two different inoculants. Several thermal parameters can be seen in
The cast applied with Ba—La inoculant presented Tensile Strength=346 MPa and 2% of carbides. On the other hand, the block applied with Sr inoculant presented Tensile Strength=361 MPa with no carbides. It shows the sensibility of the related thermal parameters on the nucleation level of the liquid batch.
Eutectic Solidification
As a remarkable solidification phenomenon, the eutectic phase represents the birth that characterizes the latter material properties. Many books and papers have approached the eutectic phase in many ways, signaling several parameters such as heat exchange between metal and mold, chemistry, graphite crystallization, recalescence, stable and meta-stable temperatures and so on.
However, the HPI alloy and its method, prescribe in the eutectic phase a specific interaction between two critical parameters directly related to the foundry process and to the cast geometry, as follows:
Pouring temperature “Tp”; and
Global solidification modulus of the cast “Mc”.
Hence applying a specific calculation, the HPI method defines the global cast modulus “Mc”, at the range: 1.38≦“Mc”≦1.52, as a function of the best calculated pouring temperature “Tp” (allowed+/−10° C.).
Such criterion allows effective speed for the eutectic cells to grow and achieve the desirable mechanical and physical properties besides drastically reduce the shrinkage formation when the HPI cast gets solid. In other words, this method requires a calculated pouring temperature as a function of the global cast modulus. It is quite different from the common practice where the pouring temperature is usually empirical in order to get the cast soundness.
Eutectoidic Solidification
As a solid-solid transformation, the eutectoidic phase shapes the final microstructure of the cast. Then, despite being a flake graphite alloy, the HPI microstructure presents slightly reduced graphite content on its matrix: ≦2.3% (calculated by the “lever rule” taking as reference the equilibrium diagram Fe—Fe3C, as shown in
Said range confirms the HPI hypoeutectic tendency that, nonetheless, keeps good machinability parameters by the increased number of eutectic cells. Also, in order to enable the obtainment of pearlite refinement, this method prescribes that the shake-out operation be done when the cast superficial temperature range is between 400° C. and 680° C., according to the cast wall thickness variation.
Said method produces some remarkable material property differences in the final microstructure, when compared with traditional gray iron. On the metallurgical diagram data,
Taking the diagram in
Remarks:
When the thick line crosses the tensile scale, the theoretical gray iron should present the uncommon value of ≈30 Kg/mm2. Instead, the HPI prototype presented the real value of 36 Kg/mm2. If we consider that a typical market gray iron hardly reaches above 28 Kg/mm2 (for cylinder blocks or heads), it is easy to observe here the first difference between both alloys.
Observing now the hardness scale on
If we still take the same theoretical gray iron with the tensile value ≈35 Kg/mm2, the related carbon equivalent value (CEL) on
The remarks above explain why we do not find on the market high resistance traditional gray iron to be used in cylinder blocks or heads; If such alloy were applied, it would present serious machinability and soundness problems (similar to CGI alloy). The purpose of the HPI alloy is exactly to fulfill such technical need.
Technical Data Comparisons Among Gray Iron Alloy (GI), HPI Alloy and CGI Alloy
Some ranges of mechanical and physical properties taken from commercial casts were followed to compare traditional gray iron (GI); high performance iron (HPI) and compact graphite iron (CGI):
According to the tests above, besides high tensile strength, the HPI alloy presents excellent machinability, damping vibration, thermal conductivity, low shrink tendency and microstructure stability (compatible with gray iron alloys).
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/BR2009/000044 | 2/12/2009 | WO | 00 | 11/18/2011 |
Publishing Document | Publishing Date | Country | Kind |
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WO2010/091486 | 8/19/2010 | WO | A |
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Number | Date | Country | |
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20120087824 A1 | Apr 2012 | US |