The present invention relates to aluminum alloys, and more particularly, to aluminum alloys used for making cast products.
Aluminum alloys are widely used, e.g., in the automotive and aerospace industries, due to a high performance-to-weight ratio, favorable corrosion resistance and other factors. Various aluminum alloys have been proposed in the past that have characteristic combinations of properties in terms of weight, strength, castability, resistance to corrosion, and cost. AlSiMgCu casting alloys are described in commonly-owned U.S. Patent Application Publication No. 2013/0105045, entitled “High-Performance AlSiMgCu Casting Alloy”, published May 2, 2013.
The disclosed subject matter relates to improved aluminum casting alloys (also known as foundry alloys) and methods for producing same. More specifically, the present application relates to new aluminum casting alloys having:
As noted above, the new aluminum casting alloys generally include 8.5-9.5 wt. % Si. In one embodiment, the aluminum alloy includes 8.75-9.5 wt. % Si. In one embodiment, the aluminum alloy includes 8.75-9.25 wt. % Si.
As noted above, the new aluminum casting alloys generally include 0.5-2.0 wt. % copper (Cu). In one approach, the aluminum alloy includes 0.8 to 2.0 wt. % copper. In another approach, the aluminum alloy includes 1.0 to 1.5 wt. % copper. In yet another approach, the aluminum alloy includes 0.7 to 1.3 wt. % copper. In another approach, the aluminum alloy includes 0.8 to 1.2 wt. % copper.
As noted above, the new aluminum casting alloys generally include 0.15-0.60 wt. % Mg. In one approach, the aluminum alloy includes 0.20-0.53 wt. % magnesium (Mg). In one approach the alloy includes ≧0.36 wt. % magnesium (e.g., 0.36-0.53 wt. % Mg). In one approach, the aluminum alloy includes from 0.40 to 0.45 wt. % magnesium. In another approach, the alloy includes ≦0.35 wt. % magnesium (e.g., 0.15-0.35 wt. % Mg). In one another approach, the alloy includes 0.20-0.25 wt. % Mg. Other combinations of magnesium and copper are described below.
The amount of copper plus magnesium may be limited to ensure an appropriate volume fraction of Q phase, as described below. For products to be processed to a T5 temper, and having 0.15-0.35 wt. % Mg (e.g., 0.20-0.25 wt. % Mg), a new aluminum casting alloy may include an amount of copper plus magnesium such that 2.5≦(Cu+10Mg)≦4.5. In one embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 2.5≦(Cu+10Mg)≦4.0. In another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 2.5≦ (Cu+10Mg)≦3.75. In yet another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 2.5≦ (Cu+10Mg)≦3.5. In another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 2.5≦(Cu+10Mg)≦3.25. In yet another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 2.75≦(Cu+10Mg)≦3.5. In any of the embodiments of this paragraph the magnesium within the aluminum alloy may be limited to 0.15-0.30 wt. % Mg, such as limited to 0.20-0.25 wt. % Mg.
For products to be processed to any of a T5, T6 or T7 temper, a new aluminum casting alloy includes an amount of copper plus magnesium such that 4.7≦(Cu+10Mg)≦5.8. In one embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 4.7≦(Cu+10Mg)≦5.7. In another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 4.7≦(Cu+10Mg)≦5.6. In yet another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 4.7≦(Cu+10Mg)≦5.5. In yet another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 4.8≦(Cu+10Mg)≦5.5. In another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 4.9≦(Cu+10Mg)≦5.5. In yet another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 5.0≦(Cu+10Mg)≦5.5. In another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 5.0≦(Cu+10Mg)≦5.4. In yet another embodiment, a new aluminum casting alloy includes an amount of copper plus magnesium such that 5.1≦(Cu+10Mg)≦5.4. In any of the embodiments of this paragraph, the magnesium within the aluminum alloy may be toward the higher end of the acceptable range, such as from 0.30-0.60 wt. % Mg, or 0.35-0.55 wt. % Mg, or 0.37-0.50 wt. % Mg. or 0.40-0.50 wt. % Mg, or 0.40-0.45 wt. % Mg. In one approach, the aluminum alloy includes about 1.0 wt. % copper (e.g., 0.90-1.10 wt. % Cu, or 0.95-1.05 wt. % Cu) in combination with about 0.4 wt. % magnesium (0.35-0.45 wt. % Mg, or 0.37-0.43 wt. % Mg).
As noted above, the new aluminum casting alloys generally include 0.35 to 0.8 wt. % manganese. In one approach, the aluminum alloy includes 0.45-0.70 wt. % Mn. In another approach, the aluminum alloy includes 0.50-0.65 wt. % Mn. In another approach, the aluminum alloy includes 0.50-0.60 wt. % Mn. In one approach, the weight ratio of iron to manganese (Fe:Mn) in the aluminum alloy is ≦0.50. In another approach, the weight ratio of iron to manganese (Fe:Mn) in the aluminum alloy is ≦0.45. In another approach, the weight ratio of iron to manganese (Fe:Mn) in the aluminum alloy is ≦0.40. In another approach, the weight ratio of iron to manganese (Fe:Mn) in the aluminum alloy is ≦0.35. In another approach, the weight ratio of iron to manganese (Fe:Mn) in the aluminum alloy is ≦0.30.
As noted above, the new aluminum casting alloys may include up to 1.0 wt. % Fe. In one approach, the aluminum alloy includes from 0.01 to 0.5 wt. % Fe. In another approach, the aluminum alloy includes from 0.01 to 0.35 wt. % Fe. In yet approach, the aluminum alloy includes from 0.01 to 0.30 wt. % Fe. In another approach, the aluminum alloy includes from 0.01 to 0.25 wt. % Fe. In yet approach, the aluminum alloy includes from 0.01 to 0.20 wt. % Fe. In another approach, the aluminum alloy includes from 0.01 to 0.15 wt. % Fe. In yet another approach, the aluminum alloy includes from 0.10 to 0.30 wt. % Fe.
As noted above, the new aluminum casting alloys may include up to 5.0 wt. % Zn. In one approach, the alloy includes ≦0.5 wt. % Zn. In another approach, the aluminum alloy includes ≦0.25 wt. % Zn. In yet another approach, the aluminum alloy includes ≦0.15 wt. % Zn. In another approach, the aluminum alloy includes ≦0.05 wt. % Zn. In yet another approach, the aluminum alloy includes ≦0.01 wt. % Zn.
As noted above, the new aluminum casting alloys may include up to 1.0 wt. % Ag. In one embodiment, the aluminum alloy includes ≦0.5 wt. % Ag. In another approach, the aluminum alloy includes ≦0.25 wt. % Ag. In yet another approach, the aluminum alloy includes ≦0.15 wt. % Ag. In another approach, the aluminum alloy includes ≦0.05 wt. % Ag. In yet another approach, the aluminum alloy includes ≦0.01 wt. % Ag.
As noted above, the new aluminum casting alloys may include up to 1.0 wt. % Ni. In one embodiment, the aluminum alloy includes ≦0.5 wt. % Ni. In another approach, the aluminum alloy includes ≦0.25 wt. % Ni. In yet another approach, the aluminum alloy includes ≦0.15 wt. % Ni. In another approach, the aluminum alloy includes ≦0.05 wt. % Ni. In yet another approach, the aluminum alloy includes ≦0.01 wt. % Ni.
As noted above, the new aluminum casting alloys may include up to 1.0 wt. % Hf. In one embodiment, the aluminum alloy includes ≦0.5 wt. % Hf In another approach, the aluminum alloy includes ≦0.25 wt. % Hf In yet another approach, the aluminum alloy includes ≦0.15 wt. % Hf In another approach, the aluminum alloy includes ≦0.05 wt. % Hf In yet another approach, the aluminum alloy includes ≦0.01 wt. % Hf.
As noted above, the new aluminum casting alloys may include up to 0.30 wt. % each of zirconium and vanadium. For high pressure die casting embodiments, both zirconium and vanadium may be present, and in an amount of at least 0.05 wt. % each, and wherein the total amount of Zr+V does not form primary phase particles (e.g., the total amount of Zr+V is from 0.10 wt. to 0.50 wt. %). In one embodiment, the aluminum alloy includes at least 0.07 wt. % each of zirconium and vanadium, and Zr+V is from 0.14 to 0.40 wt. %. In one embodiment, the aluminum alloy includes at least 0.08 wt. % each of zirconium and vanadium, and Zr+V is from 0.16 to 0.35 wt. %. In one embodiment, the aluminum alloy includes at least 0.09 wt. % each of zirconium and vanadium, and Zr+V is from 0.18 to 0.35 wt. %. In one embodiment, the aluminum alloy includes at least 0.09 wt. % each of zirconium and vanadium, and Zr+V is from 0.20 to 0.30 wt. %. In another approach, the aluminum alloy includes ≦0.03 wt. % each of zirconium and vanadium (e.g., as impurities for non-HPDC applications).
As noted above, the new aluminum casting alloys may include up to 0.30 wt. % titanium. In one embodiment, the aluminum alloy includes from 0.005 to 0.25 wt. % Ti. In another embodiment, the aluminum alloy includes from 0.005 to 0.20 wt. % Ti. In yet another embodiment, the aluminum alloy includes from 0.005 to 0.15 wt. % Ti. In another embodiment, the aluminum alloy includes from 0.01 to 0.15 wt. % Ti. In yet another embodiment, the aluminum alloy includes from 0.03 to 0.15 wt. % Ti. In another embodiment, the aluminum alloy includes from 0.05 to 0.15 wt. % Ti. When both zirconium and titanium are used in the new aluminum alloy, the aluminum alloy generally includes at least 0.005 wt. % Ti, such as any of the amounts of titanium described above. In one embodiment, the aluminum alloy includes at least 0.09 wt. % each of zirconium and vanadium, and Zr+V is from 0.18 to 0.35 wt. % and from 0.05 to 0.15 wt. % Ti.
As noted above, the new aluminum casting alloys may include up to 0.10 wt. % of one or more of strontium, sodium and antimony. In one approach, the aluminum alloy includes ≦0.05 wt. % strontium. In one approach, the aluminum alloy includes ≦0.03 wt. % sodium. In one approach, the aluminum alloy includes ≦0.03 wt. % antimony. In one embodiment, the aluminum alloy includes strontium, and from 50-300 ppm of strontium. In one embodiment, the aluminum alloy is free of sodium and antimony, and includes these elements as impurities only.
As noted above, the new aluminum casting alloys generally include other elements being ≦0.04 wt. % each and ≦0.12 wt. % in total, the balance being aluminum. In one embodiment, the new aluminum casting alloys generally include other elements being ≦0.03 wt. % each and ≦0.10 wt. % in total, the balance being aluminum
In one embodiment, the new aluminum casting alloy includes 9.14-9.41 wt. % Si, 0.54-1.53 wt. % Cu, 0.21-0.48 wt. % Mg, 0.48-0.53 wt. % Mn, 0.13-0.17 wt. % Fe, 0.11-0.30 wt. % Ti, 0.10-0.14 wt. % Zr, 0.12-0.13 wt. % V, ≦0.05 wt. % Zn, ≦0.05 wt. % Ag, ≦0.05 wt. % Ni, ≦0.05 wt. % Hf, up to 0.012 wt. % Sr, other elements being ≦0.04 wt. % each and ≦0.12 wt. % in total, the balance being aluminum. For alloys to be processed to the T5 temper, this alloy may include 0.20-0.25 wt. % Mg, and with Cu+10Mg being from 2.5 to 4.0. For alloys to be processed to any of a T5, T6 or T7 temper, this alloy may include 0.40-0.48 wt. % Mg, and with Cu+10Mg being from 4.7 to 5.8.
The new aluminum casting alloy may be shape cast in any suitable form or article. In one approach, the new aluminum alloy is shape cast in the form of an automotive component or engine component (e.g., a cylinder head or cylinder/engine block).
In one approach, a method of producing a shape cast article includes the steps of:
Regarding the introducing step (b), the mold may be any suitable mold compatible with the new aluminum casting alloy, such as a high pressure die casting (HPDC) mold.
Prior to the removing step (c), the method may include allowing the casting to solidify, and then cooling the casting. In one embodiment, the cooling step includes contacting the shape casting with water after the solidifying step. In another embodiment, the cooling step includes contacting the shape casting with air and/or water after the solidifying step. After the removing step (c), the method may include tempering the shape cast article.
In one embodiment, the tempering is tempering to a T5 temper. As defined by ANSI H35.1 (2009), the T5 temper is where an aluminum alloy is “cooled from an elevated temperature shaping process and then artificially aged. Applies to products that are not cold worked after cooling from an elevated temperature shaping process, or in which the effect of cold work in flattening or straightening may not be recognized in mechanical property limits.” When tempering to a T5 temper, the tempering step may include, after the removing step, artificially aging the shape cast article. The artificially aging may be accomplished as described below. Due to the shape casting process (e.g., HPDC), the T5 temper does not require a separate solution heat treatment and quench (i.e., is free of a separate solution heat treatment and quenching step, as are required by the T6 and T7 temper.
In another embodiment, the tempering is tempering to a T6 temper. As defined by ANSI H35.1 (2009), the T6 is where an aluminum alloy is “solution heat-treated and then artificially aged. Applies to products that are not cold worked after solution heat-treatment, or in which the effect of cold work in flattening or straightening may not be recognized in mechanical property limits.” When tempering to a T6 temper, the tempering step (d) may include (i) solutionizing of the shape cast article and subsequent (ii) quenching of the shape cast article. After the quenching step (ii), the method may include (iii) artificial aging of the shape cast article.
In yet another embodiment, the tempering is tempering to a T7 temper. As defined by ANSI H35.1 (2009), the T7 is where an aluminum alloy is “solution heat-treated and overaged/stabilized. Applies to cast products that are artificially aged after solution heat-treatment to provide dimensional and strength stability.” When tempering to a T7 temper, the tempering step (d) may include (i) solutionizing of the shape cast article and subsequent (ii) quenching of the shape cast article. After the quenching step (ii), the method may include (iii) artificially aging of the shape cast article to an overaged/stabilized condition.
In one approach, a method includes solution heat treating and quenching the aluminum alloy. In one embodiment, the solution heat treating comprises the steps of:
After the second maintaining step (d), the aluminum alloy may be quenching (e.g., in water and/or air).
As noted above, the tempering step may include artificially aging the aluminum alloy. In one embodiment, the artificially aging comprises holding the alloy at a temperature of from 190° C. to 220° C. for 1-10 hours (e.g., for about 6 hours). In another embodiment, the artificial aging is conducted at a temperature of from 175° C. to 205° C. for 1-10 hours (e.g., for about 6 hours).
To improve the performances of Al—Si—Mg—Cu cast alloys, a novel alloy design method was used and is described as follows:
In Al—Si—Mg—Cu casting alloys, increasing Cu content can increase the strength due to higher amount of θ′-Al2Cu and Q′ precipitates but reduce ductility, particularly if the amount of un-dissolved constituent Q-phase increases.
In order to minimize/eliminate un-dissolved Q-phase (AlCuMgSi) and maximize solid solution/precipitation strengthening, the alloy composition, solution heat treatment and aging practice should be optimized. In accordance with the present disclosure, a thermodynamic computation was used to select alloy composition (mainly Cu and Mg content) and solution heat treatment for avoiding un-dissolved Q-phase particles. Pandat thermodynamic simulation software and the PanAluminum database LLC, Computherm, Pandat Software and PanAluminum Database. http://www.computherm.com were used to calculate these thermodynamic data.
The inventors of the present disclosure recognize that adding Cu to Al—Si—Mg cast alloys will change the solidification sequence.
The Q-AlCuMgSi phase formation temperature (TQ) in Al-9% Si—Mg—Cu alloys is a function of Cu and Mg content. The “formation temperature” of a constituent phase is defined as the temperature at which the constituent phase starts to form from the liquid phase.
In accordance with the present disclosure, in order to completely dissolve all the as-cast Q-AlCuMgSi phase particles, the solution heat treatment temperature (TH) needs to be controlled above the formation temperature of the Q-AlCuMgSi phase, i.e., TH>TQ. The upper limit of the solution heat treatment temperature is the equilibrium solidus temperature (TS) in order to avoid re-melting. As a practical measure, the solution heat treatment temperature is controlled to be at least 5 to 10° C. below the solidus temperature to avoid localized melting and creation of metallurgical flaws known in the art as rosettes. Hence, in practice, the following relationship is established:
T
S−10° C.>TH>TQ (1)
In accordance with the present disclosure, to achieve this criterion, the alloy composition, mainly the Cu and Mg contents, should be selected so that the formation temperature of Q-AlCuMgSi phase is lower than the solidus temperature.
In accordance with the present disclosure, the preferred Mg and Cu content to maximize the alloy strength and ductility is shown in
The preferred relationship of Mg and Cu content is defined by:
Cu+10Mg=5.25 with 0.5<Cu<2.0
The upper bound is Cu+10Mg=5.8 and the lower bound is Cu+10Mg=4.7.
The foregoing approach allows the selection of a solutionization temperature by (i) calculating the formation temperature of all dissolvable constituent phases in an aluminum alloy; (ii) calculating the equilibrium solidus temperature of an aluminum alloy; (iii) defining a region in Al—Cu—Mg—Si space where the formation temperature of all dissolvable constituent phases is at least 10° C. below the solidus temperature. The Al—Cu—Mg—Si space is defined by the relative % composition of each of Al, Cu, Mg and Si and the associated solidus temperatures for the range of relative composition. For a given class of alloy, e.g., Al—Cu—Mg—Si, the space may be defined by the solidus temperature associated with relative composition of two elements of interest, e.g., Cu and Mg, which are considered relative to their impact on the significant properties of the alloy, such as tensile properties. In addition, the solutionizing temperature may be selected to diminish the presence of specific phases, e.g., that have a negative impact on significant properties, such as, tensile properties. The alloy, e.g., after casting, may be heat treated by heating above the calculated formation temperature of the phase that needs to be completely dissolved after solution heat treatment, e.g., the Q-AlCuMgSi phase, but below the calculated equilibrium solidus temperature. The formation temperature of the phase that needs to be completely dissolved after solution heat treatment and solidus temperatures may be determined by computational thermodynamics, e.g., using Pandat™ software and PanAluminum™ Database available from CompuTherm LLC of Madison, Wis.
Based on the foregoing analysis, several Mg and Cu content combinations were selected as given in Table 3. Additionally, studies by the present inventors have indicated that an addition of zinc with a concentration greater than 3 wt % to Al—Si—Mg—(Cu) alloys can increase both ductility and strength of the alloy. As shown in
A modified ASTM tensile-bar mold was used for the casting. A lubricating mold spray was used on the gauge section, while an insulating mold spray was used on the remaining portion of the cavity. Thirty castings were made for each alloy. The average cycle time was about two minutes. The actual compositions investigated are listed in Table 4, below.
The actual compositions are very close to the target compositions. The hydrogen content (single testing) of the castings is given in Table 5.
To dissolve all the Q-AlCuMgSi phase particles, the solution heat treatment temperature should be higher than the Q-AlCuMgSi phase formation temperature. Table 6 lists the calculated final eutectic temperature, Q-phase formation temperature and solidus temperature using the targeted composition of the ten alloys investigated.
Based on the above mentioned information, two solution heat treatment practices were defined and used. Alloys 2, 3, 9 and 10 had lower solidus temperature and/or lower final eutectic/Q-phase formation temperature than others. Hence a different SHT practice was used.
The practice I for alloys 2, 3, 9 and 10 was:
T
H(° C.)=570−10.48*Cu−71.6*Mg−1.3319*Cu*Mg−0.72*Cu*Cu+72.95*Mg*Mg, (2)
where, Mg and Cu are magnesium and copper contents, in wt. %. A lower limit for TH is defined by:
T
Q=533.6−20.98*Cu+88.037*Mg+33.43*Cu*Mg−0.7763*Cu*Cu−126.267*Mg*Mg (3)
An upper limit for TH is defined by:
T
S=579.2−10.48*Cu−71.6*Mg−1.3319*Cu*Mg−0.72*Cu*Cu+72.95*Mg*Mg (4)
The microstructure of the solution heat treated specimens was characterized using optical and SEM microscopy. There were no un-dissolved Q-phase particles detected in all the Cu-containing alloys investigated.
Tensile properties were evaluated according to the ASTM B557 method. Test bars were cut from the modified ASTM B108 castings and tested on the tensile machine without any further machining All the tensile results are an average of five specimens. Toughness of selected alloys was evaluated using the un-notched Charpy Impact test, ASTM E23-07a. The specimen size was 10 mm×10 mm×55 mm machined from the tensile-bar casting. Two specimens were measured for each alloy.
Smooth S-N fatigue test was conducted according to the ASTM E606 method. Three stress levels, 100 MPa, 150 MPa, and 200 MPa were evaluated. The R ratio was −1 and the frequency was 30 Hz. Three replicated specimens were tested for each condition. Test was terminated after about 107 cycles. Smooth fatigue round specimens were obtained by slightly machining the gauge portion of the tensile bar casting.
Corrosion resistance (type-of-attack) of selected conditions was evaluated according to the ASTM G110 method. Corrosion mode and depth-of-attack on both the as-cast surface and machined surface were assessed.
All the raw test data including tensile, Charpy impact and S-N fatigue are given in Tables 7 to 9. A summary of the findings is given in the following sections.
The effect of artificial aging temperature on tensile properties was investigated using the baseline alloy 1-Al-9% Si-0.5% Mg. After a minimum 4 hours of natural aging, the tensile bar castings were aged at 155° C. for 15, 30, 60 hours and at 170° C. for 8, 16, 24 hours. Three replicate specimens were used for each aging condition.
Based on the data, it is believed that the following tensile properties can be obtained with alloys aged at 155° C. for time ranged from 15 to 60 hrs.
These properties are much higher than A359 (Alloy 1) and are very similar to A201 (Al4.6Cu0.35Mg0.7Ag) cast alloy (UTS 450 MPa, TYS 380 MPa, Elongation 8%, and Q 585 MPa) ASM Handbook Volume 15, Casting, ASM International, December 2008. On the other hand, the castability of these Al-9% Si—Mg—Cu alloys is much better than A201 alloy. The A201 alloy has a poor castability due to its high tendency of hot cracking and Cu macro-segregation. Additionally, the material cost of A201 with 0.7wt % Ag is also much higher than those embodiments in accordance with the present disclosure that are Ag-free.
Based on the tensile property results, four alloys without Ag (Alloys 3, 4, 7 and 9) with promising tensile properties along with baseline alloy, A359 (Alloy 1) were selected for further investigation. Charpy impact, S-N fatigue and general corrosion tests were conducted on these five alloys aged at 155° C. for 15 hours and 60 hours.
Aluminum castings are often used in engineered components subject to cycles of applied stress. Over their commercial lifetime millions of stress cycles can occur, so it is important to characterize their fatigue life. This is especially true for safety critical applications, such as automotive suspension components.
When aged at 155° C. for 15 hours, all the Cu-containing alloys showed better fatigue performance (higher number of cycles to failure) than the baseline A359 alloy at higher stress levels (>150 MPa). At lower stress levels (<125 MPa), the fatigue lives of the Al-9Si-0.45Mg-0.75Cu and Al-9Si-0.35Mg-1.75Cu alloys are very similar to the A359 alloy, while the fatigue life of the Al-9Si-0.45Cu-0.75Cu-4Zn alloy (alloy 3) was lower than the A359 alloy. The lower fatigue life of this alloy could result from the higher hydrogen content of the casting, as stated previously.
Increasing aging time (higher tensile strength) tended to decrease the number of cycles to failure. For example, as the aging time increased from 15 hours to 60 hours, the average number of cycles to failure at 150 MPa stress level decreased from ˜323,000 to ˜205,000 for the Al-9% Si-0.45% Mg-0.75% Cu alloy and from ˜155,900 to ˜82,500 for the A359 alloy. The result could be a general trend of the strength/fatigue relationship of Al—Si—Mg—(Cu) casting alloys. Again, alloy 3 showed a lower fatigue performance than others.
More particularly,
Overall, the additions of Cu or Cu+Zn do not change the corrosion mode nor increase the depth-of—attack of the alloys. It is believed that all the alloys evaluated have similar corrosion resistance as the baseline alloy, A359.
The present disclosure has described Al—Si—Cu—Mg alloys that can achieve high strength without sacrificing ductility. Tensile properties including 450-470 MPa ultimate tensile strength, 360-390 MPa yield strength, 5-7% elongation, and 560-590 MPa Quality Index were obtained. These properties exceed conventional 3xx alloys and are very similar to that of the A201 (2xx+Ag) Alloy, while the castabilities of the new Al-9Si—MgCu alloys are much better than that of the A201 alloy. The new alloys showed better S-N fatigue resistance than A359 (Al-9Si-0.5 Mg) alloys. Alloys in accordance with the present disclosure have adequate fracture toughness and general corrosion resistance.
Because alloys such as those described in the present disclosure may be utilized in applications wherein they are exposed to high temperatures, such as in engines in the form of engine blocks, cylinder heads, pistons, etc., it is of interest to assess how such alloys behave when exposed to high temperatures.
The inventors of the present disclosure recognized that certain alloying elements, viz., Ti, V, Zr, Mn, Ni, Hf, and Fe could be introduced to the C00 alloy (previously referred to as alloy 9, e.g., in
The following table (Table 10) show 18 alloys utilizing additive elements in small quantities to the C00 alloy (previously referred to as alloy 9, e.g., in
Table 11 shows the mechanical properties of the foregoing alloys, viz., ultimate tensile strength (UTS), total yield strength (TYS) and Elongation % at 300° C., 175° C. and room temperature (RT).
High strength at elevated temperature and very good castability make the C05 alloy (TABLE 10) an excellent candidate for cylinder head applications, e.g., for internal combustion engines. Plant-scale trials for the C05 alloy (TABLE 10) were conducted. Cylinder head castings were made using a gravity semi-permanent mold casting process. The actual compositions are listed in Table 12.
Tensile specimen blocks were cut from the combustion chamber area. They were solution heat treated using following practice:
2-hr log to 940° F. (504.4° C.)+940° F.(504.4° C.)/2 hrs+30 minutes ramp up to 986° F.(530° C.)+986° F.(530° C.)/4 hrs+CWQ
Three artificial aging practices, 190° C./6 hrs, 205° C./6 hrs and 220° C./6 hrs, were evaluated and the mechanical property results are shown in Table 13.
The foregoing alloy compositions may also be used to form cylinder heads by high pressure die casting (HPDC) methods and using T5 tempering procedures.
In accordance with another embodiment of the present disclosure, the disclosed aluminum alloys may be used to cast cylinder blocks, e.g., for internal combustion engines. Since the engine block is the main contributor to engine mass, use of the disclosed alloys for the engine block may result in significant weight reduction, e.g., up to 45% weight reduction for gasoline engines, compared to engines made from cast-iron. Engines having lower mass translate into improved performance, better fuel economy and reduced emissions. For mass engine production, high-pressure die-casting (HPDC) process is widely used for high production rates and reduced production costs.
HPDC engine block casting methods frequently employ T5 temper practices. The alloys of the present disclosure may be tempered using T5 practices. Note that this approach does not employ a high-temperature solution heat treatment and quench. In accordance with an embodiment of the present disclosure, six alloys having the compositions shown in Table 14 were prepared, cast into a modified ASTM tensile bar mold.
Sixty (60) tensile bar specimens were made for each composition. After the specimens were completely solidified, half were water quenched, and the other half were air cooled. The physical attributes of the resultant specimens were then tested and are also described below. Three different artificial aging practices, 175° C./6hrs, 190° C./6hrs and 205° C./6 hrs, were evaluated for both water quenched and air-cooled specimens.
Tables 15, 16 and 17 list average yield strength, ultimate tensile strength and elongation, respectively, for air-cooled specimens aged at different conditions. Table 15 shows the effect of Cu, Mg and aging condition on yield strength of the Al-9Si-0.15Fe-0.55Mn—Cu—Mg alloys. After being completely solidified, the tensile bar castings were cooled in the air. As shown in Table 15, Mg and Cu content showed significant impact on yield strength. Alloys with 0.4% Mg and 1.0-1.5% Cu showed higher yield strength than other alloys.
Table 16 shows the effect of Cu, Mg and aging condition on ultimate tensile strength of the Al-9Si-0.15Fe-0.55Mn—Cu—Mg alloys. After being completely solidified, tensile bar castings were cooled in the air. Table 16 shows the effect of Cu, Mg and aging condition on elongation of the Al-9Si-0.15Fe-0.55Mn—Cu—Mg alloys. After being completely solidified, tensile bar castings were cooled in the air. As shown in Tables 16-17, increasing Mg and Cu will slightly increase UTS, and decrease elongation. For air cooled specimens, the highest achieved yield strength in the T5 condition was about 190 MPa.
Tables 18, 19 and 20 list average yield strength, ultimate tensile strength and elongation, respectively, for warm water quenched specimens aged at different conditions. Table 18 shows the effect of Cu, Mg and aging condition on yield strength of the Al-9Si-0.15Fe-0.55Mn—Cu—Mg alloys. After being completely solidified, the tensile bar castings were cooled in warm water. As shown in Table 18, Mg and Cu content showed significant impact on yield strength. Table 19 shows the effect of Cu, Mg and aging condition on ultimate tensile strength of the Al-9Si-0.15Fe-0.55Mn—Cu—Mg alloys. After being completely solidified, the tensile bar castings were cooled in warm water. Table 20 shows the effect of Cu, Mg and aging condition on elongation of the Al-9Si-0.15Fe-0.55Mn—Cu—Mg alloys. After being completely solidified, the tensile bar castings were cooled in warm water.
Alloys with 0.4% Mg and 1.0-1.5% Cu showed higher yield strength than other alloys. For warm water quenched specimens, the highest achieved yield strength in the T5 condition was about 260 MPa.
Additional high-pressure die-casting (HPDC) tests were completed on two alloys, the compositions of which are shown below in Table 21. The alloys were cast as journal pieces. After casting, various ones of the alloys were quenched in air, while other ones of the alloys were quenched in warm water (≈60° C.). Various ones of the alloys were aged at various times and temperatures, after which various mechanical properties were tested, the results of which are provided in Tables 22-24, below. Strength and elongation were tested using JIS14B test specimens taken from about 1 mm below the casting surface.
The fatigue properties of alloy R8 were measured at room temperature, at a stress ratio of R=−1 (=σmin/σmax) with a frequency of 1500 rpm, and with a mean stress (σm) of zero (0) MPa. The fatigue was 90 MPa at room temperature.
Fatigue strength (staircase fatigue) at about 150° C. was also measured for alloy R8 in one T5 temper, having been water quenched and artificially aged for about 6 hours at about 205° C. Alloy R8 in this type of T5 temper realized a mean fatigue strength of 81.25±7.83 MPa at 150° C. The stress amplitude increment was 5.0 MPa and the convergence factor was 0.94.
It will be understood that the embodiments described herein are merely exemplary and that a person skilled in the art may make many variations and modifications without departing from the spirit and scope of the claimed subject matter. For example, use different aging conditions may produce different resultant characteristics. All such variations and modifications are intended to be included within the scope of the appended claims.
This patent application claims priority to U.S. Provisional Patent Application No. 61/919,415, filed Dec. 20, 2013, entitled “High Performance AlSiMgCu Casting Alloy with Engine and HPDC Applications”, and International Patent Application No. PCT/US14/70938, filed Dec. 17, 2014, entitled “HIGH PERFORMANCE AlSiMgCu CASTING ALLOY”. All of the above-identified patent applications are incorporated herein by reference in their entirety.
Number | Date | Country | |
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61919415 | Dec 2013 | US |
Number | Date | Country | |
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Parent | PCT/US2014/070938 | Dec 2014 | US |
Child | 14574933 | US |