This invention is an aluminum alloy for aerospace and automotive shaped castings, castings comprised of the alloy, and methods of making cast components of the alloy.
Cast aluminum parts are used in structural applications in automobile suspensions to reduce weight. The most commonly used group of alloys, Al—Si7—Mg, has well established strength limits. In order to obtain lighter weight parts, higher strength material is needed with established material properties for design. At present, cast materials made of A356.0, the most commonly used Al—Si7—Mg alloy, can reliably guarantee ultimate tensile strength of 290 MPa (42,060 psi), and tensile yield strength of 220 MPa (31,908 psi) with elongations of 8% or greater.
A variety of alternate alloys exist and are registered that exhibit higher strength than the Al—Si7—Mg alloys. However these exhibit problems in castability, corrosion potential or fluidity that are not readily overcome. The alternate alloys are therefore less suitable for use.
Where high strength is required, forged products are often used. These are usually more expensive than cast products. There exists the potential for considerable cost savings if cast products can be used to replace forged products with no loss of strength, elongation, corrosion resistance, fatigue strength, etc. This is true in both automotive and aerospace applications.
Casting alloys exhibiting higher tensile strength and fatigue resistance than the Al—Si7—Mg material are desirable. Such improvements could be used to reduce weight in new parts or in existing parts which can be redesigned to use the improved material properties to great advantage.
The alloy of the present invention is an Al—Zn—Mg base alloy for low pressure permanent or semi-permanent mold, squeeze, high pressure die, pressure or gravity casting, lost foam, investment casting, V-mold, or sand mold casting with the following composition ranges (all in weight percent):
Silicon up to about 1.0% may be employed to improve castability. Lower levels of silicon may be employed to increase strength. For some applications, manganese up to about 0.3% may be employed to improve castability. In other alloys, manganese is to be avoided.
The alloy may also contain grain refiners such as titanium diboride, TiB2 or titanium carbide, TiC and/or anti-recrystallization agents such as zirconium or scandium. If titanium diboride is employed as a grain refiner, the concentration of boron in the alloy may be in a range from 0.0025% to 0.05%. Likewise, if titanium carbide is employed as a grain refiner, the concentration of carbon in the alloy may be in the range from 0.0025% to 0.05%. Typical grain refiners are aluminum alloys containing TiC or TiB2.
Zirconium, if used to prevent grain growth during solution heat treatment, is generally employed in a range below 0.2%. Scandium may also be used in a range below 0.3%.
In the T6 temper, the alloy demonstrated 50% higher tensile yield strength than is obtainable from A356.0-T6, while maintaining similar elongations. This will allow part designs requiring higher strength than alloys which are readily available today in Al—Si—Mg alloys such as A356.0-T6 or A357.0-T6. Fatigue performance in the T6 temper is increased over the A356.0-T6 material by 30%.
In one aspect, the present invention is an aluminum alloy including from about 3.5-5.5% Zn, from about 1-3% Mg, about 0.05-0.5% Cu and it contains less than about 1% Si.
In another aspect, the present invention is a heat treatable shaped casting of an aluminum alloy including from about 3.5-5.5% Zn, from about 1-3% Mg, from about 0.05-0.5% Cu, and less than about 1% Si.
In another aspect, the present invention is a method of preparing a heat treatable aluminum alloy shaped casting. The method includes preparing a molten mass of an aluminum alloy including from about 3.5-5.5% Zn, from about 1-3% Mg, from about 0.05-0.5% Cu, and less than about 1% Si. The method further includes casting at least a portion of the molten mass in a mold configured to produce the shaped casting, permitting the molten mass to solidify, and removing the shaped casting from the mold.
When referring to any numerical range of values herein, such ranges are understood to include each and every number and/or fraction between the stated range minimum and maximum. A range of about 3.5 to 5.5 wt % zinc, for example, would expressly include all intermediate values of about 3.6, 3.7, 3.8 and 3.9%, all the way up to and including 5.3, 5.35, 5.4, 5.475 and 5.499% Zn. The same applies to each other numerical property and/or elemental range set forth herein.
Table I presents composition data for the alloys which were tested. The first and third lines showing compositions is for directionally solidified castings. The second line is for the composition used in a shaped casting. The shaped casting was the front knuckle shown in
Table II presents room temperature mechanical properties of the directionally solidified alloys having the compositions shown in the first and third data lines of Table I. The first data line in Table II is for a directionally solidified casting comprised of the alloy of the first data line in Table I after five weeks of natural ageing. The second data line in Table 2 is for the same alloy after T5 heat treatment, and the third data line is for that alloy after T6 heat treatment. The fourth and fifth data lines in Table II are for the alloy in the bottom line of Table 1, which is a high copper alloy. This alloy, also, was subjected to a T6 heat treatment.
The development of mechanical properties of directionally solidified samples of the present invention during heat treatment is presented in
Table III presents data for front knuckle castings as shown in
It is noted that in Table III, extremely high tensile strength values and good elongation are obtained for the alloy in both T5 and T6 tempers. It is noted, again, that the composition was as presented in the second data line in Table I. The data presented in Table III are plotted in
The graph in
The samples were solution heat treated at 526° C. or 554 ° C., quenched and artificially aged at 160° C. for 6 hours. As seen earlier, the fatigue response of these samples is appreciably improved when compared to A356.0-T6 material.
The mean fatigue strength of the alloy of the present invention was 109.33 MPa with a standard deviation of 9.02 MPa. The standard deviation of the mean fatigue strength was 3.01 MPa. The calculated mean fatigue strength at 107 cycles of A356.0 T6 is 70 MPa.
Corrosion resistance of the alloy of the present invention was tested using the ASTM G110 corrosion test, which is the “Standard Practice for Evaluating Intergranular Corrosion Resistance of Heat Treatable Aluminum Alloys by Immersion in Sodium Chloride+Hydrogen Peroxide Solution”.
In this test, specimens are immersed in a solution that contains 57 g/L NaCl and 10 mL/L H2O2 (30%) for 6-24 hours. The specimens are then cross-sectioned and examined under optical microscope for type (intergranular corrosion or pitting) and depth of corrosion attack.
Corrosion tests were also performed employing the ASTM G44 test, which is the “Standard Practice for Exposure of Metals and Alloys by Alternate Immersion in Neutral 3.5% Sodium Chloride Solution”. In this test, stressed specimens are subject to a 1-hour cycle which includes immersion in 3.5% NaCl solution for 10 minutes and then in lab air for 50 minutes. This 1-hour cycle is continuously repeated. During the test, the specimens are regularly inspected for cracks and failures.
Table IV presents the compositions of various alloys according to the present invention, which were employed in ASTM G44 tests.
Table V presents the test results for the alloy compositions presented in Table IV.
Table VI and VII present the results of plant trials in which repeated shots were made from a single liquid metal reservoir. One trial was performed on April 4, one was performed on June 4 and one on September 4. On each day, the composition for all the castings made varied very little.
Table VI presents the ranges of the compositions of samples taken on each of the test days. The compositions contained high levels of magnesium and copper, which were expected to provide exceptionally high strength levels.
Table VII presents the stress data, ultimate tensile strength, tensile yield strength, and elongation for four different locations in each casting. The column for sample numbers labels the individual castings. The column for location defines individual mechanical test samples cut from the casings.
It is noted that at these high levels of magnesium and copper, excellent strength levels are obtained, with good elongation.
Having described the presently preferred embodiments of the present invention, it is to be understood that the invention may be otherwise embodied within the scope of the appended claims.
This application claims the benefit of U.S. Provisional Application Ser. No. 60/564,813 filed on Apr. 22, 2004, which is fully incorporated herein by reference thereto. It is also closely related to the patent application “A Heat Treatable Al—Zn—Mg Alloy for Shaped Castings” filed concurrently with this application, and which is also incorporated herein by reference thereto.
Number | Date | Country | |
---|---|---|---|
60564813 | Apr 2004 | US |