EP1902150B1 - Hochfeste aluminiumlegierungen und herstellungsverfahren dafür - Google Patents

Hochfeste aluminiumlegierungen und herstellungsverfahren dafür Download PDF

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Publication number
EP1902150B1
EP1902150B1 EP06849740.3A EP06849740A EP1902150B1 EP 1902150 B1 EP1902150 B1 EP 1902150B1 EP 06849740 A EP06849740 A EP 06849740A EP 1902150 B1 EP1902150 B1 EP 1902150B1
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EP
European Patent Office
Prior art keywords
alloy
degrees
product
temperature
hours
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Revoked
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EP06849740.3A
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English (en)
French (fr)
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EP1902150A1 (de
EP1902150A4 (de
Inventor
Charles E. Brooks
Ralph C. Dorward
Ray D. Parkinson
Rob A. Matuska
Mory Shaarbaf
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Kaiser Aluminum Fabricated Products LLC
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Kaiser Aluminum Fabricated Products LLC
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Application filed by Kaiser Aluminum Fabricated Products LLC filed Critical Kaiser Aluminum Fabricated Products LLC
Priority to SI200632270T priority Critical patent/SI1902150T1/en
Publication of EP1902150A1 publication Critical patent/EP1902150A1/de
Publication of EP1902150A4 publication Critical patent/EP1902150A4/de
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    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/10Alloys based on aluminium with zinc as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22FCHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
    • C22F1/00Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
    • C22F1/04Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
    • C22F1/053Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon of alloys with zinc as the next major constituent

Definitions

  • the present invention relates, in general, to a high strength aluminum alloy based on the Al-Zn-Mg-Cu alloy system and a process for forming the same.
  • the alloys are particularly suited for use in sporting goods and aerospace applications.
  • the highest strength aluminum alloys known at this time are based on the aluminum-zinc-magnesium-copper system. Such alloys are disclosed for instance in US 2005/0056353 A1
  • Commercial high-strength alloys currently being produced include AA7055 (nominally 8% Zn-2% Mg-2.2% Cu-0.10% Zr), AA7068 (nominally 7.8% Zn-2.5% Mg-2.0% Cu-0.10% Zr) and a Kaiser Aluminum alloy designated K749 (nominally 8% Zn-2.2% Mg-1.8% Cu-0.14% Zr). From the published phase relationships at 860°F for an alloy containing 8% Zn, one can note that K749 is near a phase boundary, while the other two alloys are in multiple phase fields.
  • the present invention addresses the foregoing need in a number of ways. More particularly, there are three distinct avenues for increasing an alloy's strength while maintaining its toughness: rich alloy chemistries; processing to maximize alloying effectiveness; and preventing recrystallization. Rich alloys provide more solute, which is potentially available for age hardening to higher strength levels; effective processing ensures that the solute is available for strengthening and not out of solution as second phases, which detract from fracture toughness; and maintaining an unrecrystallized microstructure optimizes both strength and toughness.
  • the present invention comprises aluminum alloys based on the Al-Zn-Mg-Cu alloy system that preferably include high levels of zinc and copper, but modest levels of magnesium. As an option, small amounts of scandium can also be employed to prevent recrystallization.
  • Each of the alloys preferably includes at least 8.5% Zn and 2.25% Cu by weight. Higher levels of each of these elements up to about 10.5% Zn and 3.0% Cu can be used. However, modestly lower amounts of Mg (max 1.85%) are preferably used to allow higher levels of the Cu.
  • the ranges of all elements in the alloys include by weight, 8.5-10.5% Zn, 1.4-1.85 % Mg, 2.25-3.0% Cu, and at least one element from the group Zr, V, or Hf not exceeding about 0.5%, the balance substantially aluminum and incidental impurities.
  • 0., optionally 0.03-0.10% Si and 0.03-0.12% Fe is also included in the alloys to prevent recrystallization.
  • toughness decreases as the total weight percentage of magnesium and copper increases. Experiments have established that the ideal range of these two elements be between 4.1 and 4.5% combined. Still further, the total weight percent of Zn, Cu and Mg is ideally between 13.0 and 14.5%.
  • a homogenization process is preferably employed after alloy ingot casting in which a slow rate of temperature increase is employed as the alloy is heated as near as possible to its melting temperature.
  • the rate of increase is limited to 20°F/hr. or less to minimize the amount of low melting point eutectic phases and thereby further enhance fracture toughness of the alloy.
  • the product is exposed to a temperature range of 175-310 degrees F for 3 to 30 hours.
  • the first step is followed by heating at 310 to 360 degrees F for 2 to 24 hours.
  • the product is heated at 175 to 300 degrees F for 1 to 30 hours.
  • the second and third aging steps can be used without the first aging step.
  • the foregoing alloys and processing operations enhance the properties of the Al-Zn-Mg-Cu alloy system, such that they can be more effectively employed in numerous applications.
  • Specific products or items in which the subject alloys can be employed include, among others, sporting goods including baseball and soft ball bats, golf shafts, lacrosse sticks, tennis rackets, and arrows; and aerospace application including aerospace components such as wing plates, bulkheads, fuselage stringers, and structural extrusions and forgings; and ordnance parts such as sabots and missile launchers.
  • a heretofore unexplored region of the Al-Zn-Mg-Cu alloy system consists of compositions comprising about 9% to 10% zinc, 2.2% to 2.8% copper, and 1.6% to 2.0% magnesium.
  • the alloy compositions listed in Table 1 were cast as 9-in. diameter billets: note that all these alloys contain about 0.05% scandium, an element which in combination with zirconium is effective in preventing recrystallization. Table 1.
  • the billets were homogenized at 880F (F means degrees Fahrenheit) and extruded to seamless 4-in. diameter tubes with a 0.305 in. wall thickness.
  • the extrusions were solution heat treated at 880F, quenched in cold water and "peak” aged to the T6 temper (24-hr soak at 250F). They were tested for tensile properties in the longitudinal direction and sections from all of the extrusions were cut and flattened to pieces about 12" square, which were also solution heat treated at 880F, quenched in cold water and peak aged. These flattened sections were tested for fracture toughness (ASTM B645) in the T-L orientation. The tensile and fracture toughness properties are listed in Table 2. Table 2.
  • FIG. 1 shows how the compositions listed in Table 1 relate to the magnesium and copper solubility limits at 885F for alloys containing a nominal zinc level of 9%.
  • compositions lying below the demarcation line between the solid solution and the Al + S phase regions are single phase alloys, which have superior fracture toughness values for a given strength level, compared to those in the 2-phase region.
  • the best combinations of strength and toughness are associated with alloys near the solvus line, which is why the 2.7% Cu/1.9% Mg composition has a relatively low toughness level.
  • the preferred compositions therefore lie within the dashed lines that run approximately parallel to the solvus. These relationships are defined by controlling the total copper plus magnesium concentrations between 4.1% and 4.5%.
  • a tube from composition #213 when drawn to a tube 2.625" in diameter with a 0.110" wall thickness and aged by a 2-step practice of 8 hr at 250F plus 4 hr at 305F had yield and tensile strengths of 100.9 ksi and 102.6 ksi, respectively.
  • the subject alloy can be over aged beyond peak strength in a second step at temperatures in the 310-360F temperature range for 2 to 24 hours to provide a desirable combination of strength and corrosion resistance.
  • Another preferred embodiment includes a final aging treatment in a third step at a lower temperature in the range 175-300F for 1 to 30 hours, which provides an additional strength benefit with no loss in corrosion properties.
  • the alloy can be subjected only to the aforementioned second and third aging steps by skipping the first step.
  • FIG. 4 compares the toughness levels of these alloys on the basis of Mg/Cu ratio with the invention alloys, using those compositions that have similar strength levels (93-95 ksi) and total Mg + Cu contents (4.0-4.2%).
  • Alloys of the compositions listed in the following table were prepared as 5" diameter billets, which were processed as described below. Although the sample alloys contained more Mg and less Cu than the preferred alloys discussed previously, it is believed that the effect of Sc addition to the alloys would be essentially the same for the preferred alloys. % by wt. Alloy No. Si Fe Cu Mg Zn Zr Sc A 0.03 0.04 1.95 2.20 8.07 0.11 0.00 B 0.03 0.05 1.86 2.17 8.05 0.00 0.22 C 0.03 0.05 1.89 2.18 8.09 0.11 0.06 D 0.03 0.04 1.84 2.12 8.11 0.12 0.11 E 0.03 0.05 1.95 2.18 8.08 0.11 0.22
  • the ingots were homogenized at 875F using a 50F/hr heating rate and air cool, and then reheated to 800F and extruded to a 0.25" by 3" flat bar. Sections of each extrusion were annealed at 775F for 3 hr, cooled 50F/hr to 450F, held 4 hr and cooled 50F/hr to room temperature. The sections were then cold rolled to 0.040" sheet using five pass reductions (84% total reduction). The sheets were solution heat treated at 885F for 30 min, quenched in cold water, and then aged to the peak strength condition (10 hr at 305F).

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  • Chemical & Material Sciences (AREA)
  • Mechanical Engineering (AREA)
  • Organic Chemistry (AREA)
  • Metallurgy (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Extrusion Of Metal (AREA)
  • Forging (AREA)
  • Golf Clubs (AREA)
  • Conductive Materials (AREA)
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Claims (18)

  1. Aluminiumlegierungsprodukt mit hoher Festigkeit und guter Zähigkeit, das bezogen auf das Gewicht 8,5 bis 10,5 % Zn, 1,4 bis 1,85 % Mg, 2,25 bis 3,0 % Cu, und höchstens 0,5 % mindestens eines Elements aus der Gruppe Zr, V oder Hf, gegebenenfalls 0,05 bis 0,30 % Sc, gegebenenfalls 0,03 bis 0,10 % Si und 0,03 bis 0,12 % Fe, den Rest Aluminium und zufällige Verunreinigungen enthält.
  2. Legierungsprodukt nach Anspruch 1, wobei die Legierung 0,05 bis 0,2 % Zr umfasst.
  3. Legierungsprodukt nach Anspruch 1, wobei die Legierung 0,05 bis 0,30 % Sc umfasst.
  4. Legierungsprodukt nach Anspruch 3, wobei die Legierung 0,05 bis 0,20 % Zr umfasst.
  5. Legierungsprodukt nach Anspruch 1, wobei die Legierung 0,03 bis 0,10 % Si und 0,03 bis 0,12 % Fe umfasst.
  6. Legierungsprodukt nach Anspruch 1, wobei die kombinierten Gewichtsprozentsätze von Mg und Cu im Bereich von 4,1 bis 4,5 % liegen.
  7. Legierungsprodukt nach Anspruch 6, wobei die kombinierten Gewichtsprozentsätze von Zn, Mg und Cu im Bereich von 13,0 bis 14,5 % liegen.
  8. Aluminiumlegierungsprodukt nach Anspruch 1, wobei das Produkt aus der Gruppe ausgewählt ist, die Sportartikel, wie beispielsweise Baseball- und Softballschläger, Golfschäfte, Lacrosse Schläger, Tennisschläger und Pfeile; Luft- und Raumfahrtkomponenten, wie beispielsweise Flügelplatten, Schotten, Rumpfstreifen und strukturelle Extrusionen und Schmiedeteile; und Militärmaterialien, wie beispielsweise Treibkäfige und Raketenwerfer, umfasst.
  9. Prozess zur Herstellung eines Aluminiumlegierungsprodukts, das 8,5 bis 10,5 % Zn, 1,4 bis 1,85 % Mg, 2,25 bis 3,0 % Cu, und höchstens 0,5 % mindestens eines Elements aus der Gruppe Zr, V oder Hf, gegebenenfalls 0,05 bis 0,30 % Sc, den Rest Aluminium und zufällige Verunreinigungen enthält, wobei das Verfahren die folgenden Schritte umfasst:
    Gießen des Legierungsprodukts, um einen Legierungsgussblock zu bilden;
    Homogenisieren des Legierungsgussblocks, um die Menge eutektischer Phasen niedrigen Schmelzpunkts darin durch Erwärmen des Gussblocks bei einer Erwärmungsrate von höchstens 11,11 °K/Std. (20 °F/Std.) von einer ersten Temperatur von mindestens 11,11 °K (20 °F) unter der Schmelztemperatur des Gussblocks auf eine zweite Temperatur von etwa 2,78 °K (5 °F) unter der Schmelztemperatur zu minimieren.
  10. Prozess nach Anspruch 9, wobei die erste Temperatur 272,04 °K (30 °F) unter der Schmelztemperatur liegt.
  11. Prozess nach Anspruch 9, wobei die erste Temperatur so ausgewählt wird, dass sie 738,71 °K (870 °F) beträgt, und die zweite Temperatur so ausgewählt wird, dass sie im Bereich von 747,04 bis 749,82 °K (885 bis 890 °F) liegt.
  12. Prozess nach Anspruch 9, wobei der Legierungsgussblock für mindestens 8 Stunden auf der ersten Temperatur gehalten wird.
  13. Prozess nach Anspruch 9, wobei die Legierung 0,05 bis 0,30 % Sc enthält.
  14. Prozess nach Anspruch 9, wobei der Legierungsgussblock zu einer Form eines Fertigprodukts geformt, bei 738,71 bis 755,37 Grad Kelvin (870 bis 900 Grad Fahrenheit) lösungsgeglüht und anschließend in einem ersten Alterungsschritt durch Erwärmen bei 352,59 bis 427,59 Grad Kelvin (175 bis 310 Grad Fahrenheit) für 3 bis 30 Stunden künstlich gealtert wird.
  15. Prozess nach Anspruch 14, wobei das Produkt durch Erwärmen bei 427,59 bis 455,37 Grad Kelvin (310 bis 360 Grad Fahrenheit) für 2 bis 24 Stunden einem zweiten Alterungsschritt unterzogen wird.
  16. Prozess nach Anspruch 15, wobei das Legierungsprodukt durch Erwärmen bei 352,59 bis 422,39 Grad Kelvin (175 bis 300 Grad Fahrenheit) für 1 bis 30 Stunden einem dritten Alterungsschritt unterzogen wird.
  17. Prozess nach Anspruch 9, wobei der Legierungsgussblock zu einer Form eines Fertigprodukts geformt, lösungsgeglüht und anschließend in einem ersten Alterungsschritt durch Erwärmen bei 427,59 bis 455,37 Grad Kelvin (310 bis 360 Grad Fahrenheit) für 2 bis 24 Stunden künstlich gealtert wird.
  18. Prozess nach Anspruch 17, wobei das Legierungsprodukt durch Erwärmen bei 352,59 bis 422,39 Grad Kelvin (175 bis 300 Grad Fahrenheit) für 1 bis 30 Stunden einem zweiten Alterungsschritt unterzogen wird.
EP06849740.3A 2005-03-24 2006-03-22 Hochfeste aluminiumlegierungen und herstellungsverfahren dafür Revoked EP1902150B1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
SI200632270T SI1902150T1 (en) 2005-03-24 2006-03-22 Aluminum alloys of high strength and process for their manufacture

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Application Number Priority Date Filing Date Title
US11/087,733 US20060213591A1 (en) 2005-03-24 2005-03-24 High strength aluminum alloys and process for making the same
PCT/US2006/010684 WO2007102831A1 (en) 2005-03-24 2006-03-22 High strength aluminum alloys and process for making the same

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EP1902150A1 EP1902150A1 (de) 2008-03-26
EP1902150A4 EP1902150A4 (de) 2016-09-07
EP1902150B1 true EP1902150B1 (de) 2018-06-20

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EP (1) EP1902150B1 (de)
CN (1) CN101193839B (de)
SI (1) SI1902150T1 (de)
WO (1) WO2007102831A1 (de)

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US9068252B2 (en) 2009-03-05 2015-06-30 GM Global Technology Operations LLC Methods for strengthening slowly-quenched/cooled cast aluminum components
US8636855B2 (en) 2009-03-05 2014-01-28 GM Global Technology Operations LLC Methods of enhancing mechanical properties of aluminum alloy high pressure die castings
US9163304B2 (en) 2010-04-20 2015-10-20 Alcoa Inc. High strength forged aluminum alloy products
CN103403894B (zh) * 2011-03-07 2016-10-26 皇家飞利浦有限公司 发光模块、灯、照明器和显示装置
US20120247623A1 (en) * 2011-04-04 2012-10-04 Matuska Robert A Optimization and Control of Metallurgical Properties During Homogenization of an Alloy
CN103572129A (zh) * 2013-11-05 2014-02-12 吴高峰 一种高尔夫球杆用铝合金制备方法
CN103572127A (zh) * 2013-11-05 2014-02-12 吴高峰 一种高尔夫球杆用铝合金
CN103572128A (zh) * 2013-11-05 2014-02-12 吴高峰 一种高尔夫球杆用铝合金及制备方法
CN103898382B (zh) * 2014-03-27 2017-01-04 北京科技大学 超强高韧耐蚀Al‐Zn‐Mg‐Cu铝合金材料及其制备方法
CN104152761A (zh) * 2014-07-31 2014-11-19 天津大学 含钪的Al-Zn-Mg-Cu-Zr合金及制备方法
CN104862551B (zh) * 2015-05-21 2017-09-29 北京科技大学 Al‑Mg‑Cu‑Zn系铝合金及铝合金板材制备方法
JP6661870B2 (ja) * 2016-05-13 2020-03-11 日本軽金属株式会社 アルミニウム合金製バット用素管及びバット並びにその製造方法
CN106422240A (zh) * 2016-11-11 2017-02-22 佛山市南海区卓航五金厂 一种兵乓球网架
CN107099706A (zh) * 2017-05-02 2017-08-29 嘉禾福顺机械实业有限公司 一种高硬度泵用合金及其制备方法
CN109266879A (zh) * 2018-11-20 2019-01-25 天津百恩威新材料科技有限公司 一种布拉磨头及高强度铝合金在制备布拉磨头中的应用
CN111519057B (zh) * 2020-05-22 2021-11-23 佛山市三水凤铝铝业有限公司 一种提高制备铝合金的模具寿命的方法
CN114346217B (zh) * 2021-12-22 2024-06-04 中山市奥博精密科技有限公司 一种金属铸件及其制备方法和应用
CN114457266A (zh) * 2021-12-27 2022-05-10 有研金属复材技术有限公司 超高强韧铸造铝合金及其成型方法

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Publication number Publication date
US20100180988A1 (en) 2010-07-22
EP1902150A1 (de) 2008-03-26
SI1902150T1 (en) 2018-08-31
WO2007102831A1 (en) 2007-09-13
CN101193839A (zh) 2008-06-04
WO2007102831A8 (en) 2007-11-29
US20060213591A1 (en) 2006-09-28
CN101193839B (zh) 2010-07-14
EP1902150A4 (de) 2016-09-07

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