High-performance 5000-series aluminum alloys

Information

  • Patent Grant
  • 11814701
  • Patent Number
    11,814,701
  • Date Filed
    Friday, September 6, 2019
    5 years ago
  • Date Issued
    Tuesday, November 14, 2023
    a year ago
Abstract
Aluminum-magnesium-manganese-zirconium-inoculant alloys that exhibit high strength, good ductility, high creep resistance, high thermal stability and durability.
Description
FIELD

This application relates to a family of 5000-series aluminum alloys with high strength, good ductility, high creep resistance, high thermal stability and durability. The disclosed alloys are especially advantageous for, but not limited to, improving performance of beverage can lids and tabs. Additionally, the disclosed alloys are, for example, advantageous for improving performance of roofing and siding materials, chemical and food equipment, storage tanks, home appliances, sheet-metal work, marine parts, transportation parts, heavy duty cooking utensils, hydraulic tubes, fuel tanks, pressure vessels, heavy-duty truck and trailer bodies and assemblies, drilling rigs, missile components, and railroad cars.


BACKGROUND

The production of aluminum cans, largely to store beverages, is the single largest usage of aluminum in the world. The annual production is a staggering 320 billion cans per year, equating to 4.16 billion kilograms of aluminum. In addition, aluminum canning is likely the world's best example of recycling, as 75% of the aluminum used in cans is recycled. The production of aluminum cans is enormous, so an efficiency improvement comes with a giant multiplicative effect; a single gram of weight saved in the can may save over 200 thousand metric tons of aluminum globally per year. Together with this weight benefit, the energy consumption as well as the CO2 emissions during transport are reduced—both key metrics in sustainability of the environment. Additionally, the lightness of aluminum cans helps save resources during filling, storage, transportation and scrap at the end of the product's life. Thus lightweighting the can has been a front-burner issue for decades.


The beverage packaging industry is constantly seeking ways to maintain the can's performance while continuing to trim the materials as much as possible. A common can design consists of two pieces: the can body is made of 3000-series aluminum, specifically AA3004, while the can lid and opener are made from 5000-series aluminum, specifically AA5182. The success behind the consistent and precise production of aluminum cans is based on the strong yet formable 3000- and 5000-series aluminum sheets. The can body is about 75% of the can's mass, while the smaller lid claims the rest, 25%. Two most obvious ways to design a lighter can are: (i) designing a smaller lid and (ii) reducing thickness of the can's wall and lid. To thin the can body and lid, stronger 3000-series and 5000-series alloys are needed, while maintaining important characteristics, such as density, formability and corrosion resistance. Aerospace-grade 2000- and 7000-series are very strong, but their low formability is not suitable for canning. Thus the common approach to develop new canning materials is to modify the currently utilized alloys, that is, modifying alloy composition and thermo-mechanical processes to the current 3000-series and 5000-series alloys to strengthen them without sacrificing other important properties. Moreover, 75% of the aluminum in cans is recycled and is currently being used to recast aluminum sheets, which are returned to can manufacturers to produce new batches of cans. Recycling plays a significant role in the economics of canning, thus modifying the current 3000-series and 5000-series alloys will help maintain the usage of low-cost recycled cans.


A well-known means to enhance the strength and maintain the ductility of commercial aluminum alloys is the addition of small concentrations of Scandium (Sc). The strengthening originates from the creation during aging of L12-structured Al3Sc nano-precipitates (˜5-10 nm in diam.) which are coherent with the aluminum matrix. The small volume fraction, nano-size and matrix coherency of these precipitates help the alloys maintain other properties, such as ductility and formability. Scandium, however, is extremely costly (ten-fold more expensive than silver), severely prohibiting its usage in cost-sensitive applications such as food and drink packaging.


Accordingly, stronger 5000-series aluminum alloys are needed, while maintaining important characteristics, such as density, formability and corrosion resistance. With a stronger material, the can's lid and tab can be made thinner, resulting in a lighter beverage can. In addition, higher performance 5000-series aluminum alloys are needed constantly in many other applications for lightweighting purposes.


SUMMARY

The embodiments described herein relate to heat-treatable aluminum-magnesium-based (5000-series) alloys, containing an Al3Zr nanoscale precipitate, wherein the nanoscale precipitate has an average diameter of about 20 nm or less and has an L12 structure in an α-Al face centered cubic matrix, wherein the average number density of the nanoscale precipitate is about 2021 m−3 or more. They exhibit high strength, good ductility, high creep resistance, high thermal stability and durability, while being essentially free of scandium (i.e., no scandium is added intentionally).





BRIEF DESCRIPTION OF THE DRAWINGS


FIGS. 1A and 1B: Microhardness evolution during (A) isochronal and (B) isothermal aging at 400° C. of Al-4.5Mg-0.35Mn-0.2Si wt. % (AA5182), Al-4.5Mg-0.35Mn-0.3Zr wt. % (AA5182+Zr) and Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % (AA5182+Zr+Sn) (invented alloy). Error bars are omitted for a few data points for the sake of figure clarity.



FIGS. 2A and 2B: (A) Bright field, two-beam transmission electron microscopy of Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % (invented alloy), and (B) higher magnification view, displaying the existence of Al3Zr nano-precipitates (circles).



FIG. 3: Microhardness evolution during isochronal aging of Al-4.5Mg-0.35Mn-0.2Si wt. % (AA5182), Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.003Sr wt. % (AA5182+Zr+Sr) (invented alloy) and Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.5Zn wt. % (AA5182+Zr+Zn) (invented alloy). Error bars are omitted for a few data points for the sake of figure clarity.



FIG. 4: Mechanical properties of Al-4.5Mg-0.35Mn-0.2Si wt. % (AA5182) and Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % (AA5182+nano-precipitates) (invented alloy), after peak-aging and cold-rolling.



FIG. 5: Microhardness of cold rolled Al-4.5Mg-0.35Mn-0.2Si wt. % (AA5182) and Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % (AA5182+nano-precipitates) (invented alloy) versus annealing temperature (1 h at each temperature).





DETAILED DESCRIPTION

5000-series aluminum alloys are strain-hardenable but not heat-treatable. They contain magnesium as the main alloying element, optionally with manganese, and typically have good strength, formability, and corrosion resistance. AA5182 aluminum alloy, containing 4-5Mg and 0.2-0.5Mn (wt. %), is currently being utilized for beverage can lids. It also is being used in automotive applications. The effect of Al3Zr nano-precipitates on the mechanical performance of this alloy was investigated. FIG. 1A displays the microhardness evolution during isochronal aging of Al-4.5Mg-0.35Mn-0.2Si wt. % (AA5182, example alloy), Al-4.5Mg-0.35Mn-0.3Zr wt. % and Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % (invented alloy). AA5182 is not heat-treatable, thus its microhardness evolution is unchanged at all temperatures. With an addition of 0.3% Zr, the microhardness evolution also appears unchanged at all temperatures. There is a slight increase in microhardness from 400 to 550° C., compared to the based AA5182 alloy, but this is within experimental error. With the addition of 0.3Zr+0.1Sn wt. %, a peak-microhardness of 86±3 HV (a 23% increase) was observed at 450° C., compared to 70±4 HV in the based AA5182 alloy. This is a strong indication of Al3Zr nano-precipitates, which are known to form around this temperature and enhance strength. This is corroborated by the microhardness evolution during isothermal at 400° C., as shown in FIG. 1B, of these three alloys. Microhardness of the base AA5182 alloy is unchanged, while it starts to increase after aging for 24 h with addition of Zr. In the Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % invented alloy, it increases rapidly during aging and peaks at 24 h, reaching ˜90±5 KV (a 29% increase), compared to 70±5 HV in the based AA5182 alloy. It should be noted that an addition of only Zr, without an inoculant (Sn), is not sufficient to generate a high number density of Al3Zr nano-precipitates, hence the strength increase due to Zr addition, without Sn, is not significant. The precipitate structure of the peak-aged Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % invented alloy is displayed in FIGS. 2A and 2B. Three different populations of precipitates, Al6Mn, hexagonal α-Al(Mn, Fe)Si, and Al3Zr nano-precipitates, are observed. Fe is present in the alloy as an impurity element. The first two populations appear in a low number density, whereas a high number density of Al3Zr nano-precipitates is observed.



FIG. 3 displays the microhardness evolution during isochronal aging of Al-4.5Mg-0.35Mn-0.2Si wt. % (AA5182), Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.003Sr wt. % (invented alloy) and Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.5Zn wt. % (invented alloy). With an addition of 0.3Zr+0.003Sr wt. %, there is a significant increase in microhardness from 250 to 500° C., reaching 82±4 HV (a 19% increase), compared to the based AA5182 alloy. With an addition of 0.3Zr+0.5Zn wt. %, there is also a significant increase in microhardness from 400 to 550° C., reaching 82±3 HV (a 19% increase), compared to the based AA5182 alloy. This is a strong indication of the formation of Al3Zr nano-precipitates, assisted by either Sr or Zn, which enhances strength.


Mechanical properties of Al-4.5Mg-0.35Mn-0.2Si wt. % (AA5182) and Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % (invented alloy), after peak-aging and cold rolling are displayed in FIG. 4. Both strength and elongation of the AA5182, with addition of nano-precipitates, are increased compared to the based AA5182 alloy. An increase of 12% in yield strength, 8% in tensile strength, and 26% in elongation are observed.


Additionally, FIG. 5 suggests that the recrystallization temperature is at ˜250° C. for cold-rolled Al-4.5Mg-0.35Mn-0.2Si wt. % (AA5182) and at ˜300° C. for cold-rolled Al-4.5Mg-0.35Mn-0.2Si-0.3Zr-0.1Sn wt. % (invented alloy), containing nano-precipitates (an increase of 50° C.). This suggests that Al3Zr nano-precipitates suppresses the recrystallization, by pinning the movement of grain boundaries via Zener pinning.


Table 1 lists mechanical properties of thin sheets (0.25 mm in thickness) of Al-4.5Mg-0.25Mn-0.2Fe-0.09Si wt. % (AA5182) in hard-temper (example alloy 1) and soft temper (example alloy 2), Al-4.5Mg-0.25Mn-0.2Fe-0.09Si-0.3Zr-0.1Sn wt. % (AA5182-nano) in hard-temper (invented alloy 1) and soft temper (invented alloy 2). AA5182 hard-temper is a common aluminum alloy for beverage can lids, whereas AA5182 soft-temper is commonly used in automotive applications. The AA5182-nano alloy, in both hard- and soft-tempers (invented alloys 1 and 2) achieve higher yield strength and tensile strength, while maintaining essentially the same elongation at break, compared to the AA5182 alloy with the respective tempers (example alloy 1 and 2). The thin sheets of the alloys in Table 1 were fabricated by the following steps: casting, hot-rolling, annealing, cold-rolling, and stabilizing heat treatment for hard-temper; and casting, hot-rolling, cold rolling, and annealing for soft-temper.













TABLE 1







Yield
Tensile
Elongation



strength
strength
at break



(MPa)
(MPa)
(%)



















AA5182 - hard temper
355 ± 6
412 ± 7
6-8


(example alloy 1)


AA5182-nano - hard temper
390 ± 6
450 ± 8
6-8


(invented alloy 1)


AA51.82 - soft temper
170 ± 5
315 ± 6
20-25


(example alloy 2)


AA5182-nano - soft, temper
200 ± 4
330 ± 7
20-25


(invented alloy 2)









The disclosed aluminum alloys are essentially free of scandium, which is understood to mean that no scandium is added intentionally. Addition of scandium in aluminum alloys is advantageous for mechanical properties. For example, it is described in U.S. Pat. No. 5,624,632, which is incorporated herein by reference. However, scandium is very expensive (ten times more expensive than silver), severely limiting its practical applications.


Zirconium, with a concentration of up to about 0.3 wt. %, is sometimes added to aluminum alloys for grain refining. The refined grain structure helps improve castability, ductility, and workability of the final product. An example is described in U.S. Pat. No. 5,976,278, which is incorporated herein by reference. In the present application, zirconium with a concentration of less than about 0.5 wt. %, and preferably less than about 0.4 wt. %, is added together with an inoculant element to form Al3Zr nano-precipitates, wherein the nanoscale precipitate has an average diameter of about 20 nm or less and has an L12 structure in an α-Al face centered cubic matrix, and wherein the average number density of the nanoscale precipitate is about 2021 m−3 or more, with a purpose to improve mechanical strength, ductility, creep resistance, thermal stability and durability of the based alloys. Generally, a zirconium concentration of more than about 0.2 wt. % is needed so that Zr atoms have enough driving force to form Al3Zr nano-precipitates.


Disclosed aluminum alloys comprise an inoculant, wherein the inoculant comprises one or more of tin, strontium, zinc, gallium, germanium, arsenic, indium, antimony, lead, and bismuth. The presence of an inoculant accelerates precipitation kinetics of Al3Zr nano-precipitates, thus these precipitates can be formed within a practical amount of time during heat-treatment. In the other words, the beneficial Al3Zr nano-precipitates can be formed within a few hours of heat treatment, with the presence of the inoculant, compared to between a few weeks and a few months of heat treatment without the presence of an inoculant. Among all inoculant elements, tin appears to be the best performer in terms of accelerating precipitation kinetics of Al3Zr nano-precipitates. A tin concentration of less than about 0.2% is needed for the mentioned purpose. Beyond this value, tin will form bubbles and/or a liquid phase in the aluminum solid matrix, which is detrimental for the mechanical properties. For example, this behavior is described in U.S. Pat. No. 9,453,272, which is incorporated herein by reference.


In one embodiment, an aluminum alloy comprises aluminum, magnesium, manganese, silicon, zirconium, and an inoculant, and including a nanoscale precipitate comprising Al3Zr, wherein the nanoscale precipitate has an average diameter of about 20 nm or less and has an L12 structure in an α-Al face centered cubic matrix, wherein the average number density of the nanoscale precipitate is about 2021 m−3 or more, and wherein the inoculant comprises one or more of tin, strontium, and zinc.


In one embodiment, if an aluminum alloy is in hard temper it possesses a yield strength of at least about 380 MPa, a tensile strength of at least about 440 MPa, and an elongation at least about 5% at room temperature.


In one embodiment, if an aluminum alloy is in soft temper it possesses a yield strength of at least about 190 MPa, a tensile strength of at least about 320 MPa, and an elongation of at least about 18% at room temperature.


In one embodiment, an aluminum alloy possesses a recrystallization temperature of about 300° C.


In one embodiment, an aluminum alloy comprises about 3.0 to about 6.2% by weight magnesium; about 0.01 to about 1.8% by weight manganese; about 0.01 to about 0.2% by weight silicon; about 0.2 to about 0.5% by weight zirconium; about 0.01 to about 0.2% by weight tin; and aluminum as the remainder.


In one embodiment, an aluminum alloy comprises about 3.0 to about 6.2% by weight magnesium; about 0.01 to about 1.8% by weight manganese; about 0.01 to about 0.2% by weight silicon; about 0.2 to about 0.5% by weight zirconium; about 0.001 to about 0.1% by weight strontium; and aluminum as the remainder.


In one embodiment, an aluminum alloy comprises about 3.0 to about 6.2% by weight magnesium; about 0.01 to 1.8% by weight manganese; about 0.01 to about 0.2% by weight silicon; about 0.2 to about 0.5% by weight zirconium; about 0.1 to about 1% by weight zinc; and aluminum as the remainder.


In one embodiment, an aluminum alloy comprises a plurality of L12 precipitates having an average diameter of about 10 nm or less.


In one embodiment, an aluminum alloy comprises a plurality of L12 precipitates having an average diameter of about 3 nm to about 7 nm.


In one embodiment, an aluminum alloy comprises about 4.5% by weight magnesium, about 0.35% by weight Manganese, about 0.2% by weight silicon, about 0.3% by weight zirconium, about 0.1% by weight tin, and aluminum as the remainder.


In one embodiment, an aluminum alloy comprises about 4.5% by weight magnesium, about 0.35% by weight manganese, about 0.2% by weight silicon, about 0.3% by weight zirconium, about 0.003% by weight strontium, and aluminum as the remainder.


In one embodiment, an aluminum alloy comprises about 4.5% by weight magnesium, about 0.35% by weight manganese, about 0.2% by weight silicon, about 0.3% by weight zirconium, about 0.5% by weight zinc, and aluminum as the remainder.


In one embodiment, an aluminum alloy comprises no more than about 0.5% iron as an impurity element.


In one embodiment, an aluminum alloy comprises aluminum, magnesium, manganese, silicon, zirconium, and an inoculant, and including a nanoscale precipitate comprising Al3Zr, wherein the nanoscale precipitate has an average diameter of about 20 nm or less and has an L12 structure in an α-Al face centered cubic matrix, wherein the average number density of the nanoscale precipitate is about 2021 m−3 or more, and wherein the inoculant comprises one or more of gallium, germanium, arsenic, indium, antimony, lead, and bismuth.


One method for manufacturing a component from a disclosed aluminum alloy comprises: a) melting the alloy at a temperature of about 700 to about 900° C.; b) then casting the melted alloy into casting molds at ambient temperature; c) then using a cooling medium to cool the cast ingot; and d) then heat aging the cast ingot at a temperature of about 350° C. to about 450° C. for a time of about 2 to about 48 hours. In one embodiment, the method further comprises cold rolling the cast ingot to form a sheet product. In one embodiment, the method further comprises a final stabilizing heat treatment of the sheet product at a temperature of about 140° C. to about 170° C. for a time of about 1 to about 5 hours. In some embodiments, the cooling medium can be air, water, ice, or dry ice. The heat aging step stated above (350-450° C. for 2-48 hours) is determined to be peak-aging for components comprising the disclosed aluminum alloys. When a component manufactured from a disclosed aluminum alloy is peak-aged, the microstructure of the component is thermally stable and is unchanged by exposure to elevated temperatures for extended times.


Another method for manufacturing a component from a disclosed aluminum alloy comprises: a) melting the alloy at a temperature of about 700 to 900° C.; b) then casting the alloy into casting molds at ambient temperature; c) then using a cooling medium to cool the cast ingot; and d) then hot rolling the cast ingot into a sheet. In one embodiment, the method further comprises then heat aging the sheet at a temperature of about 350° C. to about 450° C. for a time of about 2 to about 48 hours. In one embodiment, the method further comprises then cold rolling the sheet, after the heat aging step, to form a thin sheet or foil product. In one embodiment, the method further comprises a final stabilizing heat treatment of the thin sheet or foil product at a temperature of about 140° C. to about 170° C. for a time of about 1 to about 5 hours.


Another method for manufacturing a component from a disclosed aluminum alloy comprises: a) melting the alloy at a temperature of about 700 to 900° C.; b) then casting the alloy into casting molds at ambient temperature; c) then using a cooling medium to cool the cast ingot; d) then hot rolling the cast ingot into a sheet; e) then cold rolling the sheet to form a thin sheet or foil product; and f) then heat aging the thin sheet or foil product at a temperature of about 300° C. to about 410° C. for a time of about 2 to about 24 hours.


Some applications for the disclosed alloys include, for example, beverage can lids, beverage can tabs, roofing materials, siding materials, chemical manufacturing equipment, food manufacturing equipment, storage tanks, home appliances, sheet-metal work, marine parts, transportation parts, heavy duty cooking utensils, hydraulic tubes, fuel tanks, pressure vessels, truck bodies, truck assemblies, trailer bodies, trailer assemblies, drilling rigs, missile components, and railroad cars. Some fabricated forms of the disclosed aluminum alloys include, for example, wires, sheets, plates and foils.


From the foregoing, it will be understood that numerous modifications and variations can be effectuated without departing from the true spirit and scope of the novel concepts of the present invention. It is to be understood that no limitation with respect to the specific embodiments illustrated and described is intended or should be inferred.

Claims
  • 1. An aluminum alloy comprising: 3.0 to 6.2% by weight magnesium;0.01 to 1.8% by weight manganese;0.01 to 0.2% by weight silicon;0.2 to 0.5% by weight zirconium;an inoculant, wherein the inoculant is: (a) 0.01 to 0.2% by weight tin; or(b) 0.001 to 0.1 by weight strontium; andaluminum as the remainder;wherein the alloy includes a nanoscale precipitate comprising Al3Zr;wherein the nanoscale precipitate has an average diameter of about 20 nm or less and has an L12 structure in an α-Al face centered cubic matrix; andwherein the average number density of the nanoscale precipitate is about 1021 m−3 or more.
  • 2. The aluminum alloy of claim 1, comprising: about 3.0 to about 6.2% by weight magnesium;about 0.01 to about 1.8% by weight manganese;about 0.01 to about 0.2% by weight silicon;about 0.2 to about 0.5% by weight zirconium;about 0.01 to about 0.2% by weight tin; andaluminum as the remainder.
  • 3. The aluminum alloy of claim 1, comprising: about 3.0 to about 6.2% by weight magnesium;about 0.01 to about 1.8% by weight manganese;about 0.01 to about 0.2% by weight silicon;about 0.2 to about 0.5% by weight zirconium;about 0.001 to about 0.1% by weight strontium; andaluminum as the remainder.
  • 4. The aluminum alloy of claim 1, wherein the plurality of L12 precipitates has an average diameter of about 10 nm or less.
  • 5. The aluminum alloy of claim 1, wherein the plurality of L12 precipitates has an average diameter of about 3 nm to about 7 nm.
  • 6. The aluminum alloy of claim 1, comprising: about 4.5% by weight magnesium;about 0.35% by weight manganese;about 0.2% by weight silicon;about 0.3% by weight zirconium;about 0.1% by weight tin; andaluminum as the remainder.
  • 7. The aluminum alloy of claim 1, comprising: about 4.5% by weight magnesium;about 0.25% by weight manganese;about 0.09% by weight silicon;about 0.2% by weight iron;about 0.3% by weight zirconium;about 0.1% by weight tin; andaluminum as the remainder.
  • 8. The aluminum alloy of claim 1, comprising: about 4.5% by weight magnesium;about 0.35% by weight manganese;about 0.2% by weight silicon;about 0.3% by weight zirconium;about 0.003% by weight strontium; andaluminum as the remainder.
  • 9. The aluminum alloy of claim 1, comprising: about 4.5% by weight magnesium;about 0.35% by weight manganese;about 0.2% by weight silicon;about 0.3% by weight zirconium;about 0.5% by weight zinc; andaluminum as the remainder.
  • 10. The aluminum alloy of claim 1, wherein the alloy possesses a recrystallization temperature of about 300° C.
  • 11. The aluminum alloy of claim 1, wherein the alloy is essentially free of scandium.
  • 12. The aluminum alloy of claim 1, wherein the alloy comprises no more than about 0.5% iron as an impurity.
  • 13. A beverage can lid comprising the aluminum alloy of claim 1.
  • 14. A beverage can tab comprising the aluminum alloy of claim 1.
  • 15. An aluminum alloy component comprising the aluminum alloy of claim 1, wherein the aluminum alloy component is selected from a group consisting of roofing materials, siding materials, chemical manufacturing equipment, food manufacturing equipment, storage tanks, home appliances, sheet-metal work materials, marine parts, transportation parts, heavy duty cooking utensils, hydraulic tubes, fuel tanks, pressure vessels, truck bodies, truck assemblies, trailer bodies, trailer assemblies, drilling rigs, missile components, and railroad cars.
  • 16. A fabricated form of the aluminum alloy of claim 1, the fabricated form selected from a group consisting of wires, sheets, plates and foils.
  • 17. The aluminum alloy of claim 1, wherein when the aluminum alloy is in hard temper, it possesses a yield strength of at least about 380 MPa, a tensile strength of at least about 440 MPa, and an elongation of at least about 5% at room temperature; and when the aluminum alloy is in soft temper, it possesses a yield strength of at least about 190 MPa, a tensile strength of at least about 320 MPa, and an elongation of at least about 18% at room temperature.
Parent Case Info

This application is a continuation of International Patent Application No. PCT/US2018/020899, filed Mar. 5, 2018, and titled High-Performance 5000-Series Aluminum Alloys, which claims the benefit of and priority to U.S. Provisional Patent Application No. 62/468,467, filed Mar. 8, 2017, and titled High-Performance 5000-Series Aluminum Alloys, the contents of each of which are incorporated herein by reference in their entirety. This invention was made with government support under Federal Award No. IIP 1549282, awarded by National Science Foundation. The Government has certain rights in the invention.

Government Interests

This invention was made with government support under Federal Award No. IIP 1549282, awarded by National Science Foundation. The Government has certain rights in the invention.

US Referenced Citations (33)
Number Name Date Kind
3551143 Marukawa et al. Dec 1970 A
3807969 Schoerner et al. Apr 1974 A
5087301 Angers et al. Feb 1992 A
5327955 Easwaran Jul 1994 A
5449421 Hamajima et al. Sep 1995 A
5908518 Hoffmann et al. Jun 1999 A
5976214 Kondoh et al. Nov 1999 A
6149737 Hattori et al. Nov 2000 A
6592687 Lee et al. Jul 2003 B1
6918970 Lee et al. Jul 2005 B2
8323373 Haynes, III et al. Dec 2012 B2
8778099 Pandey Jul 2014 B2
9453272 Vo et al. Sep 2016 B2
10697046 Sanaty-Zadeh et al. Jun 2020 B2
20010025675 Haszler et al. Oct 2001 A1
20030192627 Lee et al. Oct 2003 A1
20040091386 Carroll et al. May 2004 A1
20040177902 Mergen et al. Sep 2004 A1
20040256036 Van Der Hoeven et al. Dec 2004 A1
20040261922 Van Der Hoeven et al. Dec 2004 A1
20090263275 Pandey Oct 2009 A1
20100143177 Pandey et al. Jun 2010 A1
20110017359 Pandey Jan 2011 A1
20120000578 Wang et al. Jan 2012 A1
20130183189 Bishop et al. Jul 2013 A1
20130199680 Apelian et al. Aug 2013 A1
20130220497 Huskamp et al. Aug 2013 A1
20150259773 Vo et al. Sep 2015 A1
20150284825 Norman et al. Oct 2015 A1
20150284831 Kropfl et al. Oct 2015 A1
20160271688 Wuest et al. Sep 2016 A1
20170058386 Vo et al. Mar 2017 A1
20180010215 Sanaty-Zadeh et al. Jan 2018 A1
Foreign Referenced Citations (22)
Number Date Country
1555423 Dec 2004 CN
101649405 Feb 2010 CN
103233147 Aug 2013 CN
103866167 Jun 2014 CN
103924175 Jul 2014 CN
105525162 Apr 2016 CN
107475648 Dec 2017 CN
0 558 957 Sep 1993 EP
0610006 Aug 1994 EP
0799900 Oct 1997 EP
1138794 Oct 2001 EP
2 241 644 Oct 2010 EP
H02117704 May 1990 JP
H05331587 Dec 1993 JP
H11507102 Jun 1999 JP
2002105573 Apr 2002 JP
2004250738 Sep 2004 JP
2008-025006 Feb 2008 JP
WO-03010349 Feb 2003 WO
WO 2010085888 Aug 2010 WO
WO-2014088449 Jun 2014 WO
WO-2015119021 Aug 2015 WO
Non-Patent Literature Citations (55)
Entry
Non-Final Office Action dated Jun. 26, 2020 for U.S. Appl. No. 15/263,011, 7 pages.
Extended European Search Report dated Sep. 21, 2020 for European Application No. 18763441.5, 8 pages.
Non-Final Office Action dated May 4, 2016 for U.S. Appl. No. 14/645,654, 8 pages.
Non-Final Office Action dated Dec. 31, 2018 for U.S. Appl. No. 15/263,011, 5 pages.
Final Office Action dated Aug. 8, 2019 for U.S. Appl. No. 15/263,011, 7 pages.
Ex Parte Quayle Office Action mailed Aug. 19, 2019 for U.S. Appl. No. 15/642,798, 5 pages.
Extended European Search Report dated Feb. 15, 2017 for European Application No. 15760733.4, 9 pages.
Extended European Search Report dated Sep. 23, 2019 for European Application No. 19172652.0, 8 pages.
International Search Report and Written Opinion dated Jun. 25, 2016 for International Application No. PCT/US2015/020218, 14 pages.
International Search Report and Written Opinion dated Jun. 15, 2018 for International Application No. PCT/US2018/020899, 10 pages.
Berezina, A. L. et al., “Decomposition Processes in the Anomalous Supersaturated Solid Solution of Binary and Ternary Aluminum Alloys Alloyed with Sc and Zr,” Acta Physica Polonica A, 122(3):539-543 (2011).
Booth-Morrison, C. et al., “Effect of Er additions on ambient and high-temperature strength of precipitation-strengthened Al—Zr—Sc—Si alloys,” Acta Mater, 60:3463-3654 (2012).
Booth-Morrison, C. et al., “Role of silicon in accelerating the nucleation of Al3(Sc,Zr) precipitates in dilute Al—Sc—Zr alloys,” Acta Mater, 60:4740-4752 (2012).
Booth-Morrison, C. et al., “Coarsening resistance at 400° C of precipitation-strengthened AlZrScEr Alloys,” Acta Mater, 59(18):7029-7042 (2011).
Carroll, M. C. et al., “Effects of minor Cu additions on a Zn-modified Al-5083 alloy,” Materials Science and Engineering, A319-321:425-428 (2001).
Carroll, M. C. et al., “Effects of Zn Additions on the Grain Boundary Precipitation and Corrosion of Al-5083,” Spripta Mater., 42:335-340 (2000).
Carroll, M. C. et al., “Optimum Trace Copper Levels for SCC Resistance in a Zn-Modified Al-5083 Alloy,” Materials Science Forum, 396-402:1443-1448 (2002).
Fuller, C. B. et al., “Temporal evolution of the nanostructure of Al(Sc,Zr) alloys: Part 1—Chemical compositions of Al3(Sc1−xZrx) precipitates,” Acta Mater, 53:5401-5413 (2005).
Hallem, H. et al., “The formation of Al3(ScxZryHf1−x−y) dispersoids in aluminum alloys,” Mater Sci Eng A, 421:154-160 (2006).
Hori, S et al., “Effect of small addition of Si on the precipitation of Al—0.6%Zr Alloys,” J Jpn Inst Light Met, 28:79-84(1978).
Huang, H. et al., “Age Hardening Behavior and Corresponding Microstructure of Dilute Al—Er—Zr Alloys,” Metallurgical and Materials Transactions A, 44A:2849-2856 (2013).
Knipling, K. E. et al., “Criteria for developing castable, creep-resistant aluminum-based alloys—a Review,” Z Metallkd, 97:246-265 (2006).
Knipling, K. E. et al., “Atom Probe Tomographic Studies of Precipitation in Al—0.1Zr—0.1Ti (at.%) Alloys,” Microscopy and Microanalysis, 13:1-14 (2007).
Knipling, K. E. et al., “Nucleation and Precipitation Strengthening in Dilute Al—Ti and Al—Zr Alloys,” Metallurgical and Materials Transactions A, 38A:2552-2563 (2007).
Knipling, K. E. et al., “Creep resistance of cast and aged Al—0.1 Zr and Al—0.1Zr—0.1Ti (at.%) alloys at 300-400° C,” Scrpta Materialia, 59:387-390 (2008).
Knipling, K. E. et al., “Precipitation evolution in Al—Zr and Al—Zr—Ti alloys during isothermal aging at 375-425° C,” Acta Mater, 56:114-127 (2008).
Knipling, K. E. et al., “Precipitation evolution in Al—Zr and Al—Zr—Ti alloys during isothermal aging at 450-600° C,” Acta Mater, 56:1182-1195 (2008).
Knipling, K. E. et al., “Precipitation evolution in Al—0.1Sc, Al—0.1 Zr and Al—0.1Sc—0.1Zr (at.%) alloys during isochronal aging,” Acta Mater, 58:5184-5195 (2010).
Knipling, K. E. et al., “Ambient- and high-temperature mechanical properties of isochronally aged Al—0.06Sc, Al—0.06Zr and Al—0.06Sc—0.06Zr (at.%) alloys,” Acta Mater, 59:943-954 (2011).
Kumar, N. et al., “Microstructure and mechanical behavior of friction stir processed ultrafine grained Al—Mg—Sc alloy,” Materials Science and Engineering A, 528:5883-5887 (2011).
Kumar, N. et al., “Critical grain size for change in deformation behavior in ultrafine grained Al—Mg—Sc alloy,” Scr Mater, 64:576-579 (2011).
Kumar, N. & Mishra, R. S., “Thermal stability of friction stir processed ultrafine grained Al—Mg—Sc alloy,” Materials Characterization, 74:1-10 (2012).
LeClaire, A. D. et al., “3.2.13 Aluminum group metals,” Diffusion in Solid Metals and Alloys (H. Mehrer (Ed.)), Springer Materials—Landolt-Börnstein—Group III condensed Matter, 26:151-156 (1990).
Li, H. et al., “Precipitation and evolution and coarsening resistance at 400° C of Al microalloyed with Zr and Er,” Scr Mater, 67:73-76 (2012).
Ohashi, T. et al., “Effect of Fe and Si on age hardening properties of supersaturated solid solution of Al—Zr,” J Jpn. Inst Met, 34:604-640 (1970).
Riddle, Y. W. et al., “A Study of Coarsening, Recrystallization, and Morphology of Microstructure in Al—Sc—(Zr)—(Mg) Alloys,” Metallurgical and Materials Transactions A, 35A:341-350 (2004).
Sato, T. et al., “Effects of Si and Ti Additions on the Nucleation and Phase Stability of the L12-Type Al3Zr Phase in Al—Zr Alloys,” Mater Sci Forum, 217-222:895-900 (1996).
Seidman, D. N. et al., “Precipitation strengthening at ambient and elevated temperatures of heat-treatable Al(Sc) alloys,” Acta Mater, 50:4021-4035 (2002).
Unocic, K. A. et al., “Grain Boundary Precipitate Modification for Improved Intergranular Corrosion Resistance,” Materials Science Forum, 519-521:327-332 (2006).
Van Dalen, M. E. et al., “Effects of Ti additions on the nanostructure and creep properties of precipitation-strengthened Al—Sc alloys,” Acta Mater, 53:4225-4235 (2005).
Wen, S. P. et al., “Synergetic effect of Er and Zr on the precipitation hardening of Al—Er—Zr alloy,” Scr Mater, 65:592-595 (2011).
Zhang, Y. et al., “Precipitation evolution of Al—Zr—Yb alloys during isochronal aging,” Scr Mater, 69:477-480 (2013).
Court, S. A. et al., “The Ageing and Thermal Recovery Behaviour of Al—Mg—Cu Alloys,” Materials Science Forum, vols. 396-402, pp. 1031-1036, 2002. doi:10.4028/www.scientific.net/MSF.396-402.1031.
Final Office Action dated Feb. 24, 2021 for U.S. Appl. No. 15/263,011, 7 pages.
Furu, T. et al., “Trace Elements in Aluminium Alloys:Their Origin and Impact on Processability and Product Properties,” Proceedings of the 12th International Conference on Aluminium Alloys, Sep. 5-9, 2010, Yokohama, Japan, pp. 282-289, 2010.
International Search Report and Written Opinion dated Oct. 5, 2021 for International Application No. PCT/US2021/030676, 27 pages.
Morishita, M. et al., “Prediction method of crack sensitivity during DC casting of Al—Mn and Al—Mg series aluminum alloys,” Journal of Japan Institute of Light Metals, vol. 59, No. 8, 2009, pp. 417-423. Abstract.
Nisancioglu, K., “Significance of Trace Element Segregation in Corrosion of Aluminum Alloys,” Proceedings of the 12th International Conference on Aluminium Alloys, Sep. 5-9, 2010, Yokohama, Japan, pp. 1455-1462, 2010.
Non-Final Office Action dated Dec. 21, 2021 for U.S. Appl. No. 15/263,011, 7 pages.
Notice of Reasons for Rejection dated Feb. 1, 2022 for Japanese Application No. 2019-548274, with English translation, 11 pages.
Notice of Reasons for Rejection dated Nov. 8, 2022 for Japanese Application No. 2019-548274, with English translation, 7 pages.
Office Action dated Aug. 13, 2021 for Korean Application No. 10-2016-7028392, with English translation, 14 pages.
Office Action dated Dec. 15, 2020 for Chinese Application No. 201880025144.9, with English translation, 24 pages.
Office Action dated Sep. 9, 2021 for Chinese Application No. 201880025144.9, with English translation, 7 pages.
Zhu, Z. & Starink, M. J., “Age hardening and softening in cold-rolled Al—Mg—Mn alloys with up to 0.4 wt% Cu,” Materials Science and Engineering A, 489:138-149 (2008).
Related Publications (1)
Number Date Country
20190390306 A1 Dec 2019 US
Provisional Applications (1)
Number Date Country
62468467 Mar 2017 US
Continuations (1)
Number Date Country
Parent PCT/US2018/020899 Mar 2018 US
Child 16562981 US