The 7XXX wrought Al—Zn-based alloys are commonly used in structural applications demanding high specific strength. Compared to wrought alloys, castings decrease the fabrication cost and associated logistics lead time, because castings enable near-net-shape products. However, the known 7XXX alloys are susceptible to hot tearing during solidification and therefore not optimal for casting. The hot tearing is caused by a relatively high thermal expansion coefficient and significant volumetric difference between liquid and solid.
Senkov et al. [U.S. Pat. No. 7,060,139 (incorporated by reference herein)] disclose a high-strength aluminum alloy with a nominal composition of Al—6.0˜12.0 Zn—2.0˜3.5 Mg—0.1˜0.5 Sc—0.05˜0.20 Zr—0.5˜3.0 Cu—0.10˜0.45 Mg—0.08˜0.35 Fe—0.07˜0.20 Si, in wt %. The alloy by Senkov et al. shows high tensile strength while maintaining high elongation in ambient temperatures and cryogenic temperatures. The freezing range of the alloy by Senkov et al. is about 164 to about 195° C., the solidus temperature about 422 to about 466° C., and the eutectic phase fraction about 1.1 to about 1.5%. However, the alloy shows poor casting characteristics. Thus, there has developed a need for new 7XXX aluminum casting alloys that are resistant to hot tearing. Such alloys would be useful for articles of manufacture such as hydrogen turbo pump housing or other aerospace materials.
In a principal aspect, the present invention comprises high-strength aluminum casting alloys that are resistant to hot tearing. The yield strength of the casting alloys ranges from about 410 MPa to about 540 MPa, at room temperature. The invented alloys are Al—Zn-based and comprise the major alloying elements Sc, Zr, Mg, and Cu. The amounts of Sc and Zr are optimized to produce primary L12-phase particles which refine the grain size and improve the hot-tearing resistance as well as fatigue resistance and toughness. The amounts of Zn, Mg, and Cu are optimized for high resistance to hot-tearing and high strength. The amounts of Fe, Mn, and Si are kept low and at a minimum because these elements have a detrimental effect on strength and hot-tearing resistance.
To produce primary L12-phase particles, the solvus temperature of the L12 phase must be above the solvus temperature of the fcc phase. The solvus temperatures can be computed with thermodynamic database and calculation packages such as Thermo-Calc® software version N offered by Thermo-Calc Software. Alternatively, in the composition space of the alloys, the solvus temperatures can be approximated by the following equations:
L12 solvus=87.01×wpSc+157.89×wpZr−243.43×wpSc×wpZr+267.06×wpSc0.14+769.51×wpZr0.05
fcc solvus=−1.76×wpZn−5.14×wpMg−0.005×wpZn×wpMg+139.13×wpZn0.002+792.11×wpMg0.0002
where wpSc, wpZn, wpZr, and wpMg are the weight percentages of Sc, Zr, Zn, and Mg, respectively. These equations are based on the best fit for solvus temperatures.
Additionally, the amount of Zr is kept below about 0.3 wt % to minimize the formation of Al3Zr which has a D023 crystal structure. As shown by Hyde in Al—0.5Sc—0.4Zr (wt %), D023 particles quickly grow too large [Hyde, K. 2001. The Addition of Scandium to Aerospace Casting Alloys. Ph.D. diss., University of Manchester (incorporated herewith)], and are not very effective for refining the fcc grain size. In the discovered alloys, small Al3(Sc, Zr) particles with an L12 crystal structure are employed instead to inoculate small fcc grains during melt cooling. Because Zr is an inexpensive substitute for Sc in L12, the alloys of the invention use as much Zr as possible, about 0.25±0.05 wt %. However, where cost is not a limiting factor, as little as 0.15 wt % Zr can be used in combination with a larger amount of Sc.
The amounts of Sc and Zr in the casting alloys are optimized for cooling rates up to about 100° C. per second. The L12-Al3(Sc, Zr) particle size distribution depends on the melt cooling rate. Casting into a sand mold results in a cooling rate of about 0.5° C. per second. Higher cooling rates are accessible through direct-chill casting where the billet is cooled, for example, with water during solidification. Cooling rates above about 100° C. per second are accessible through casting methods such as the Continuous Rheoconversion Process (CRP).
As shown in
Because hot tearing is caused substantially by a thermal contraction during solidification, resistance to hot tearing can be improved by decreasing the freezing range and increasing the solidus temperature below which the aluminum alloy is completely solid. It is also helpful to increase the eutectic phase fraction formed at late stages of solidification, because the eutectic phase solidifies completely at one temperature and reduces the amount of melt contracting over the freezing range.
Solidification parameters such as the freezing range, the solidus temperature, and the eutectic phase fraction can be computed with thermodynamic database and calculation packages such as Thermo-Calc software. To compute solidification parameters of complex alloy systems with Thermo-Calc software, the Gibbs free energy of relevant phases must be assessed following the CALPHAD (CALculation of PHAse Diagrams) approach. One such relevant phase is the metastable η′ phase, because the 7 XXX wrought alloys employ q′ phase precipitates for strengthening. For efficient strengthening, the mean radius of η′ precipitate should be less than about 5 nm.
The η′ phase precipitation kinetics can be simulated with PrecipiCalc® software version 0.9.2 offered by QuesTek Innovations LLC after assessing the thermodynamic description. The predicted particle size distribution can be used as input to a mechanistic model of the yield strength, which comprises contributions from precipitation strengthening, grain-size strengthening, solid-solution strengthening, and dislocation strengthening. The amounts of Zn, Mg, and Cu of the alloys are chosen to optimize the solidification parameters at various yield strength levels.
The amounts of Fe, Mn, and Si are kept as low as possible because these elements otherwise form large insoluble constituent particles of Al13Fe4, Al7Cu2Fe, Mg2Si, and Al6Mn which negatively affect the toughness, fatigue, and SCC resistance. The amount of Fe is preferably kept below about 0.0075 wt %, Mn below about 0.2 wt %, and Si below about 0.03 wt %.
In order to avoid incipient melting during homogenization or solution treatment, the homogenization or solution treatment temperature should be below the final solidification temperature, preferably with a safety margin of about 10 to 30° C. A two-step treatment distinguishing the homogenization from the solution treatment, as shown in
The subject matter of the invention is applicable to aluminum 7XXX alloys in particular, but the invention is not necessarily so limited. Thus, one benefit of the invention is to eliminate, or substantially eliminate, hot tearing of cast aluminum alloys.
Further benefits, advantages and features of the invention are set forth herein.
In the detailed description which follows references will be made to the drawing comprising the following figures:
______ Yield strength iso-contours (ksi)
% Eutectic (Scheil)
______ Scheil Freezing range (° C.)
- - - Scheil solidification temperature (° C.)
Star: High strength solution (YS˜80 ksi)
Triangle: Medium strength solution (YS˜70 ksi)
Square: Low strength solution (YS˜60 ksi)
Following are specific examples of the invention.
A melt was prepared comprising Al—6.3 Zn—3.2 Mg—1.1 Cu—0.52 Sc—0.20 Zr, in wt %. The exemplary alloy preferably includes a variance in the constituents in the range of plus or minus ten percent of the mean value. The alloy was cast through the CRP reactor into a sand-casting mold at measured cooling rates of 50˜100° C./second. As shown in
A rectangular panel of alloy A was cast successfully without hot tearing. The melt was degassed with argon for 45 minutes at 700˜720° C. and then reheated to 740° C. just prior to mold pouring. The mold measured about 1 cm in depth. The pouring time to fill the mold was approximately 20 seconds. The mold filled successfully, producing a panel suitable for characterization. Following the breakout from the mold, removal of all gating and cleaning, the panel was shipped to UES, Inc. at the Wright Patterson Air Force Base for characterization.
A melt was prepared comprising Al—5.3 Zn—3.0 Mg—1.1 Cu—0.55 Sc—0.25 Zr, in wt %. The exemplary alloy preferably includes a variance in the constituents in the range of plus or minus ten percent of the mean value. The alloy was cast through the CRP reactor into a sand-casting mold at a measured cooling rate of 100° C./second. As shown in
A melt was prepared comprising Al—4.5 Zn—2.3 Mg—0.62 Cu—0.42 Sc—0.25 Zr, in wt %. The exemplary alloy preferably includes a variance in the constituents in the range of plus or minus ten percent of the mean value. The alloy was cast through the CRP reactor into a sand-casting mold. As shown in
Table 1 summarizes the compositions of the examples set forth above and sets forth the general range of the constituents for the practice of the invention in weight percent:
Table 2 summarizes the information with respect to the microstructural elements of the examples set forth above and considered relevant to the range of the constituents in the practice of the invention.
While embodiments of the invention have been disclosed, the scope thereof is not so limited and the invention is to be limited only by the following claims and equivalents thereof.
Activities relating to the development of the subject matter of this invention were funded at least in part by United States Government and thus may be subject to license rights and other rights in the United States, specifically contract number FA8650-05-C-5800.
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/US09/31251 | 1/16/2009 | WO | 00 | 7/15/2010 |
Number | Date | Country | |
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61021503 | Jan 2008 | US |