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(11) |
EP 1 902 150 B1 |
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EUROPEAN PATENT SPECIFICATION |
| (45) |
Mention of the grant of the patent: |
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20.06.2018 Bulletin 2018/25 |
| (22) |
Date of filing: 22.03.2006 |
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International Patent Classification (IPC):
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| (86) |
International application number: |
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PCT/US2006/010684 |
| (87) |
International publication number: |
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WO 2007/102831 (13.09.2007 Gazette 2007/37) |
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HIGH STRENGTH ALUMINUM ALLOYS AND PROCESS FOR MAKING THE SAME
HOCHFESTE ALUMINIUMLEGIERUNGEN UND HERSTELLUNGSVERFAHREN DAFÜR
ALLIAGES D'ALUMINIUM À RÉSISTANCE ÉLEVÉE ET PROCÉDÉ DE FABRICATION CORRESPONDANT
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| (84) |
Designated Contracting States: |
|
AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC NL PL PT RO SE
SI SK TR |
| (30) |
Priority: |
24.03.2005 US 87733
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| (43) |
Date of publication of application: |
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26.03.2008 Bulletin 2008/13 |
| (73) |
Proprietor: Kaiser Aluminum Fabricated Products, LLC |
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Foothill Ranch, CA 92610 (US) |
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Inventors: |
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- BROOKS, Charles, E.
Chandler, AZ 85249 (US)
- DORWARD, Ralph, C.
Escalon, CA 95320 (US)
- PARKINSON, Ray, D.
Livermore, CA 94550 (US)
- MATUSKA, Rob, A.
Heath, OH 43056 (US)
- SHAARBAF, Mory
Jackson, TN 38301 (US)
|
| (74) |
Representative: Stiel, Jürgen |
|
Patentanwalt Stiel
Geissleite 32 97289 Thüngen 97289 Thüngen (DE) |
| (56) |
References cited: :
US-A1- 2002 150 498 US-A1- 2004 099 352 US-B1- 6 627 014
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US-A1- 2002 162 609 US-A1- 2005 056 353 US-B2- 6 462 120
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| Note: Within nine months from the publication of the mention of the grant of the European
patent, any person may give notice to the European Patent Office of opposition to
the European patent
granted. Notice of opposition shall be filed in a written reasoned statement. It shall
not be deemed to
have been filed until the opposition fee has been paid. (Art. 99(1) European Patent
Convention).
|
Background Of The Invention
1. Field of the Invention
[0001] 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. Although not limited
thereto, the alloys are particularly suited for use in sporting goods and aerospace
applications.
2. Description of the Background Art
[0002] 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. In the latter case all the alloying elements are not in solid
solution at 860°F, and are not only unavailable for age hardening, but the undissolved
phases remaining after heat treatment detract from toughness. Although solution heat
treating at a higher temperature than 860°F will dissolve more of the solute, care
has to be taken to ensure that the alloy does not undergo eutectic melting, which
is a common problem in commercially cast alloys that have locally enriched regions
as a result of microsegregation that occurred during casting.
[0003] There is a need in many applications, such as sporting goods and aerospace applications,
for even stronger alloys based on the aluminum-zinc-magnesium-copper system that do
not sacrifice toughness. However, this requirement presents a problem because, in
general, as the tensile strength of an aluminum alloy is increased, its toughness
decreases.
Summary of the Invention
[0004] 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.
[0005] To provide increased tensile strength without sacrificing toughness through the use
of rich chemistries, 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. In the preferred embodiments, 0., optionally 0.03-0.10%
Si and 0.03-0.12% Fe is also included in the alloys to prevent recrystallization.
Additionally, it has been found that 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%.
[0006] To maximize alloying effectiveness during formation of the alloys, 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.
In particular, for the last 20-30°F below the 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. Once the ingot
is formed into finished shape using extrusion and rolling steps, for example, the
product is preferably solution heat treated at 870 to 900 degrees F and then artificially
aged. The aging process can be carried out by exposing the product to a one, two or
three step heat treatment process. In the first step, the product is exposed to a
temperature range of 175-310 degrees F for 3 to 30 hours. In the optional second step,
the first step is followed by heating at 310 to 360 degrees F for 2 to 24 hours. Finally,
in the third optional step, the product is heated at 175 to 300 degrees F for 1 to
30 hours. As a still further option, the second and third aging steps can be used
without the first aging step.
[0007] 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.
Brief Description of the Drawings
[0008] The features and advantages of the present invention will become apparent form the
following detailed description of a preferred embodiment thereof, taken in conjunction
with the accompanying drawings, in which:
FIG. 1 is a graph depicting T6 strength (YTS and UTS) as a function of the total alloy
content in weight percent for a number of sample alloys formed in accordance with
the preferred embodiments;
FIG. 2 is a graph depicting fracture toughness as a function of combined percentages
of Cu and Mg for sample alloys formed in accordance with the preferred embodiments;
FIG. 3 is an equilibrium diagram which depicts the phase relationships at 885°F as
a function of percentages of Cu and Mg for an alloy formed in accordance with the
preferred embodiments that contains 9% Zn;
FIG. 4 is a graph illustrating the effect of the ratio of Mg to Cu on fracture toughness
for the alloys formed in accordance with the preferred embodiments;
FIG. 5 is a graph depicting second phase volume percent as a function of heating rate
in a formation process for Alloy AA7068; and
FIG. 6 is a graph illustrating the effect of scandium on strength of an Al-8% Zn-2.2%
Mg-1.9% Cu alloy.
Detailed Description of the Preferred Embodiments
[0009] The following examples illustrate how alloy modifications and efficient processing
operations can be used to enhance the properties of the Al-Zn-Mg-Cu alloy system in
accordance with the preferred embodiments of the present invention, such that they
can be more effectively utilized in sporting goods and aerospace applications.
Example 1
[0010] 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. Alloy compositions
| |
Percent by Weight |
| Alloy |
Si |
Fe |
Cu |
Mg |
Zn |
Zr |
Sc |
| 179 |
0.04 |
0.07 |
2.47 |
1.83 |
8.87 |
0.14 |
0.06 |
| 180 |
0.04 |
0.09 |
2.71 |
1.89 |
8.95 |
0.13 |
0.06 |
| 189 |
0.04 |
0.08 |
2.14 |
1.89 |
8.60 |
0.12 |
0.05 |
| 190 |
0.03 |
0.09 |
2.31 |
1.86 |
9.21 |
0.13 |
0.05 |
| 191 |
0.03 |
0.11 |
2.35 |
1.81 |
9.63 |
0.13 |
0.05 |
| 192 |
0.04 |
0.10 |
2.33 |
1.87 |
10.13 |
0.12 |
0.05 |
| 200 |
0.04 |
0.09 |
2.58 |
1.64 |
8.84 |
0.12 |
0.05 |
| 202 |
0.04 |
0.12 |
2.46 |
1.66 |
8.87 |
0.13 |
0.05 |
| 203 |
0.04 |
0.10 |
2.69 |
1.78 |
8.94 |
0.13 |
0.05 |
| 204 |
0.03 |
0.10 |
2.88 |
1.58 |
8.78 |
0.12 |
0.05 |
| 209 |
0.04 |
0.08 |
2.64 |
1.49 |
8.78 |
0.14 |
0.05 |
| 213 |
0.03 |
0.07 |
2.42 |
1.63 |
9.65 |
0.13 |
0.05 |
| 214 |
0.03 |
0.09 |
2.56 |
1.44 |
9.50 |
0.14 |
0.05 |
| 215 |
0.04 |
0.09 |
2.57 |
1.73 |
9.82 |
0.12 |
0.05 |
| 216 |
0.03 |
0.10 |
2.81 |
1.60 |
9.65 |
0.13 |
0.05 |
[0011] 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. Tensile and fracture toughness properties
| %Zn |
%Cu |
%Mg |
Strength (ksi) |
Toughness (ksi rt.in) |
| UTS |
YTS |
Kg |
Kp |
| 8.60 |
2.14 |
1.89 |
97.1 |
88.5 |
25.2 |
30.5 |
| 9.21 |
2.31 |
1.86 |
100.1 |
93.9 |
22.4 |
27.5 |
| 9.63 |
2.35 |
1.81 |
99.9 |
94.2 |
20.9 |
25.4 |
| 10.13 |
2.33 |
1.87 |
103.2 |
97.8 |
21.2 |
24.0 |
| 8.87 |
2.47 |
1.83 |
101.1 |
92.2 |
20.9 |
23.9 |
| 8.95 |
2.71 |
1.89 |
102.9 |
93.7 |
20.1 |
20.5 |
| 8.84 |
2.58 |
1.64 |
98.6 |
93.8 |
23.1 |
25.8 |
| 8.87 |
2.46 |
1.66 |
98.4 |
92.8 |
25.3 |
22.2 |
| 8.94 |
2.69 |
1.78 |
100.0 |
94.2 |
24.2 |
22.4 |
| 8.78 |
2.88 |
1.58 |
99.1 |
93.8 |
24.8 |
21.9 |
| 8.78 |
2.64 |
1.49 |
96.4 |
91.9 |
24.8 |
22.9 |
| 9.65 |
2.42 |
1.63 |
100.3 |
96.3 |
24.7 |
21.3 |
| 9.50 |
2.56 |
1.44 |
98.5 |
94.9 |
26.2 |
21.2 |
| 9.82 |
2.57 |
1.73 |
102.6 |
98.2 |
21.9 |
18.2 |
| 9.65 |
2.81 |
1.60 |
100.6 |
97.1 |
20.0 |
18.4 |
[0012] As can be seen from Table 2, tensile yield strengths well in excess of 90 ksi were
obtained in most of the alloys, with two compositions achieving about 98 ksi. As shown
in FIG. 1, strength correlated well with the total alloy content, with each wt. pct.
adding about 4.8 ksi to the yield strength. The equilibrium phase relations at the
homogenizing and solution heat treatment temperature explain the reason for this behavior.
FIG. 3 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
(i.e., the solvus) 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%.
[0013] Although the properties described above were obtained with a "standard" T6 temper
aging treatment by exposing the shaped products to heat of between 175 and 310F for
3 to 30 hours (24 hr at 250F was specifically used), as with most Al-Zn-Mg-Cu alloys,
other practices may also be advantageous, depending on the desired combination of
properties. For example, 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. Similarly, 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. As yet another alternative, the alloy can be
subjected only to the aforementioned second and third aging steps by skipping the
first step.
Example 2
[0014] To compare the invention alloy with other commercial high-zinc alloys such as AA7036,
AA7056 and AA7449, which have higher Mg/Cu ratios in the range 1.0 to 1.4, the following
alloys were prepared as described in Example 1.
Table 3. Compositions of Comparative Alloys
| |
Percent by Weight |
| Alloy No. |
Si |
Fe |
Cu |
Mg |
Zn |
Zr |
Sc |
| 36 |
0.03 |
0.06 |
1.91 |
2.17 |
9.02 |
0.15 |
0.05 |
| 39 |
0.04 |
0.05 |
1.28 |
2.74 |
9.02 |
0.13 |
0.06 |
| 43 |
0.03 |
0.03 |
1.44 |
2.62 |
9.04 |
0.13 |
0.05 |
| 47 |
0.04 |
0.06 |
1.59 |
2.34 |
8.95 |
0.14 |
0.06 |
[0015] The yield strengths and toughness values for these alloys are listed in the following
table.
Table 4. Mechanical Properties of Comparative Alloys
| Alloy |
Mg/Cu Ratio |
%(Mg+Cu) |
Yield Strength (ksi) |
Kpmax (ksi rtin.) |
| 36 |
1.14 |
4.08 |
94.9 |
24.5 |
| 47 |
1.47 |
3.93 |
93.9 |
22.7 |
| 43 |
1.77 |
3.99 |
93.9 |
21.3 |
| 39 |
2.14 |
4.02 |
92.7 |
20.2 |
[0016] 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%).
Example 3
[0017] As noted earlier it is important that undissolved second phases do not remain after
processing so that fracture toughness can be maximized. This is especially important
in alloys that are rich in alloy content, and lie near an equilibrium solvus phase
boundary. To illustrate how homogenizing practice can affect the amount of such undissolved
phase(s), samples of as-cast AA7068 alloy billet were heated from 850F at various
rates in a differential scanning calorimeter (DSC), and the energy associated with
eutectic melting, which started at about 885F was measured. This energy measurement
is directly proportional to the amount of undissolved second phase remaining at the
incipient melting point, and the relationship between these factors has been determined
by quantitative microscopy. FIG. 5 shows how heating rate affects the amount of this
phase as determined from the DSC data.
[0018] Note that a slow heating rate of about 10F/hr reduces the amount of second phase
to a level below 1 vol.%. One would expect that a ∼5F/hr heating rate would reduce
the "soluble" portion to near zero. We also note that for heating rates of 10-20F/hr,
the volume fraction of undissolved eutectic is no greater than the amount of insoluble
Fe-containing constituent (independent of heating rate or homogenization temperature)
at a nominal 0.12% Fe level (approx. 1 vol.%).
Example 4
[0019] It has been recognized for a number of years that scandium in combination with zirconium
is an effective recrystallization inhibitor. A Russian review article states "it is
desirable to add scandium to aluminum alloys in a quantity from 0.1 to 0.3% together
with zirconium (0.05-0.15%)". However, "the greatest effect.... is observed for alloys
not containing alloy elements combining with scandium in insoluble phases...; with
a limited copper content [scandium combines with copper] alloying with scandium together
with zirconium of Al-Zn-Mg-Cu and Al-Cu-Li alloys is possible". As such, "commercial
alloys based on Al-Zn-Mg-Sc-Zr (01970, 01975) have been developed".
[0020] Two potential drawbacks to scandium additions to 7XXX alloys containing about 2%
copper are evident:
- 1) the copper level is high enough to combine with scandium, thereby rendering it
ineffective, and
- 2) the high price of scandium; at the 0.2% level it would add about $10 a pound to
the cost of the aluminum alloy.
[0021] It would therefore be economically and technically attractive if scandium levels
could be effectively used below those recommended in the Russian literature.
[0022] 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 |
[0023] 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). The as-extruded bars were also heat treated similarly and both products
were tested for transverse tensile properties, as listed below. The specific effects
of scandium on strength are also shown in FIG. 6.
| Alloy No. |
%Zr |
%Sc |
UTS (ksi) |
Yield Strength (ksi) |
| Extrusion |
Sheet |
Extrusion |
Sheet |
| A |
0.11 |
0 |
94.7 |
90.7 |
91.4 |
87.8 |
| B |
0 |
0.22 |
88.2 |
92.0 |
86.1 |
88.4 |
| C |
0.11 |
0.06 |
95.7 |
97.1 |
92.2 |
93.3 |
| D |
0.12 |
0.11 |
95.2 |
96.6 |
92.2 |
93.3 |
| E |
0.11 |
0.22 |
94.5 |
96.5 |
91.1 |
92.5 |
[0024] A number of points are evident from these results:
- 1. The strongest alloy in both extrusion and sheet form contains 0.06% Sc (with 0.11%
Zr)
- 2. At the 0.1% Zr level, 0.06% Sc is effective in raising the strength of the sheet
product by about 6 ksi.
- 3. 0.22% Sc in the absence of zirconium raises the strength of the sheet product by
only 1 ksi, and lowers the extrusion strength by about 6 ksi. The effectiveness of
only 0.06% Sc in preventing recrystallization was confirmed by comparing the microstructures
of the sheet products containing (a) 0.11% Zr, (b) 0.11% Zr + 0.06% Sc, and (c) 0.22%
Sc (no Zr) .
In view of the foregoing, the preferred range in the alloys for Sc is 0.05-0.30%,
with a more preferred range of 0.05-0.10%.
[0025] It is to be understood that within the scope of the appended claims, the invention
may be practiced otherwise than as specifically described above.
1. An aluminum alloy product having high strength with good toughness, containing 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 0.5%, optionally 0.05-0.30% Sc, optionally 0.03-0.10%
Si and 0.03-0.12% Fe, the balance aluminum and incidental impurities.
2. The alloy product of claim 1, wherein said alloy contains 0.05-0.2% Zr.
3. The alloy product of claim 1, wherein said alloy includes 0.05-0.30% Sc.
4. The alloy product of claim 3, wherein said alloy includes 0.05-0.20% Zr.
5. The alloy product of claim 1, wherein said alloy includes 0.03-0.10% Si and 0.03-0.12%
Fe.
6. The alloy product of claim 1, wherein the combined weight percentages of Mg and Cu
range from 4.1 to 4.5%.
7. The alloy product of claim 6, wherein the combined weight percentages of Zn, Mg and
Cu range from 13.0 to 14.5%.
8. The aluminum alloy product of claim 1, wherein said product is selected from the group
including sporting goods such as baseball and soft ball bats, golf shafts, lacrosse
sticks, tennis rackets, and arrows; aerospace components such as wing plates, bulkheads,
fuselage stringers, and structural extrusions and forgings; and ordnance parts such
as sabots and missile launchers.
9. A process for making an aluminum alloy product containing 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
0.5%, optionally 0.05-0.30% Sc the balance aluminum and incidental impurities, said
method including the steps of:
casting said alloy product to form an alloy ingot; and
homogenizing said alloy ingot to minimize the amount of low melting point eutectic
phases therein by heating said ingot at a heating rate of no more than 11.11°K/hr.
(20°F/hr.) from a first temperature at least 11.11 (20°F) below the melting temperature
of said ingot to a second temperature of about 2.78 °K (5°F) below said melting temperature.
10. The process of claim 9, wherein said first temperature is 272.04°K (30°F) below said
melting temperature.
11. The process of claim 9, wherein said first temperature is selected to be 738.71°K
(870°F) and said second temperature is selected to be in the range of 747.04-749.82°K
(885-890°F).
12. The process of claim 9 where the alloy ingot is held at said first temperature for
at least 8 hours.
13. The process of claim 9, wherein said alloy contains 0.05-0.30% Sc.
14. The process of claim 9, wherein said alloy ingot is formed into a shape of a finished
product, solution heat treated at 738.71 to 755.37 degrees K (870 to 900 degrees F)
and then artificially aged in a first aging step by being heated at 352.59 to 427.59
degrees K (175-310 degrees F) for 3 to 30 hours.
15. The process of claim 14, wherein said product is exposed to a second aging step by
being heated at 427.59 to 455.37 degrees K (310 to 360 degrees F) for 2 to 24 hours.
16. The process of claim 15, wherein said alloy product is exposed to a third aging step
by being heated at 352.59 to 422.39 degrees K (175 to 300 degrees F) for 1 to 30 hours.
17. The process of claim 9, wherein said alloy ingot is formed into a shape of a finished
product, solution heat treated and then artificially aged in a first aging step by
being heated at 427.59 to 455.37 degrees K (310 to 360 degrees F) for 2 to 24 hours.
18. The process of claim 17, wherein said alloy product is exposed to a second aging step
by being heated at 352.59 to 422.39 degrees K (175 to 300 degrees F) for 1 to 30 hours.
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.
1. Produit en alliage d'aluminium ayant une résistance élevée et une bonne dureté, contenant
en poids, de 8,5 à 10,5 % de Zn, de 1,4 à 1,85 % de Mg, de 2,25 à 3,0 % de Cu, et
au moins un élément du groupe Zr, V, ou Hf n'excédant pas 0,5 %, éventuellement de
0,05 à 0,30 % de Sc, éventuellement de 0,03 à 0,10 % de Si et de 0,03 à 0,12 % de
Fe, le reste étant de l'aluminium et des impuretés incidentes.
2. Produit en alliage selon la revendication 1, dans lequel ledit alliage contient de
0,05 à 0,2 % de Zr.
3. Produit en alliage selon la revendication 1, dans lequel ledit alliage contient de
0,05 à 0,30 % de Sc.
4. Produit en alliage selon la revendication 3, dans lequel ledit alliage contient de
0,05 à 0,20 % de Zr.
5. Produit en alliage selon la revendication 1, dans lequel ledit alliage contient de
0,03 à 0,10 % de Si et de 0,03 à 0,12 % de Fe.
6. Produit en alliage selon la revendication 1, dans lequel les pourcentages en poids
combinés de Mg et Cu sont dans la plage de 4,1 à 4,5 %.
7. Produit en alliage selon la revendication 6, dans lequel les pourcentages en poids
combinés de Zn, Mg et Cu sont dans la plage de 13,0 à 14,5 %.
8. Produit en alliage d'aluminium selon la revendication 1, dans lequel ledit produit
est choisi dans le groupe comprenant les articles de sport tels que les battes de
baseball et de softball, les clubs de golf, les bâtons de jeu de crosse, les raquettes
de tennis, et les flèches ; les composants pour l'industrie aérospatiale tels que
les plaques d'ailes, les cloisons étanches, les raidisseurs de fuselage, et les extrusions
et les pièces forgées structurales ; et les pièces d'artillerie telles que les sabots
et les lanceurs de missiles.
9. Procédé de fabrication d'un produit en alliage d'aluminium contenant de 8,5 à 10,5
% de Zn, de 1,4 à 1,85 % de Mg, de 2,25 à 3,0 % de Cu, et au moins un élément du groupe
Zr, V, ou Hf n'excédant pas 0,5 %, éventuellement de 0,05 à 0,30 % de Sc, le reste
étant de l'aluminium et des impuretés incidentes, ledit procédé comprenant les étapes
de :
coulage dudit produit en alliage pour former un lingot en alliage ; et
homogénéisation dudit lingot en alliage pour réduire au minimum la quantité de phases
eutectiques à bas points de fusion par chauffage dudit lingot à une vitesse de chauffage
inférieure ou égale à 11,11 °K/h (20 °F/h) depuis une première température au moins
11,11 °K (20 °F) au-dessous de la température de fusion dudit lingot jusqu'à une seconde
température environ 2,78 °K (5 °F) au-dessous de ladite température de fusion.
10. Procédé selon la revendication 9, dans lequel ladite première température est 272,04
°K (30 °F) au-dessous de ladite température de fusion.
11. Procédé selon la revendication 9, dans lequel ladite première température est choisie
pour être de 738,71 °K (870 °F) et ladite seconde température est choisie pour être
dans la plage de 747,04 à 749,82 °K (885 à 890 °F).
12. Procédé selon la revendication 9 dans lequel le lingot en alliage est maintenu à ladite
première température pendant au moins 8 heures.
13. Procédé selon la revendication 9, dans lequel ledit alliage contient de 0,05 à 0,30
% de Sc.
14. Procédé selon la revendication 9, dans lequel ledit lingot en alliage est formé en
fonction de la forme du produit fini, soumis à un traitement thermique de mise en
solution de 738,71 à 755,37 degrés K (870 à 900 degrés F) puis artificiellement vieilli
dans une première étape de vieillissement par chauffage de 352,59 à 427,59 degrés
K (175 à 310 degrés F) pendant 3 à 30 heures.
15. Procédé selon la revendication 14, dans lequel ledit produit est exposé à une deuxième
étape de vieillissement par chauffage de 427,59 à 455,37 degrés K (310 à 360 degrés
F) pendant 2 à 24 heures.
16. Procédé selon la revendication 15, dans lequel ledit produit en alliage est exposé
à une troisième étape de vieillissement par chauffage de 352,59 à 422,39 degrés K
(175 à 300 degrés F) pendant 1 à 30 heures.
17. Procédé selon la revendication 9, dans lequel ledit lingot en alliage est formé en
fonction de la forme du produit fini, soumis à un traitement thermique de mise en
solution puis artificiellement vieilli dans une première étape de vieillissement par
chauffage de 427,59-455,37 degrés K (310 à 360 degrés F) pendant 2 à 24 heures.
18. Procédé selon la revendication 17, dans lequel ledit produit en alliage est exposé
à une seconde étape de vieillissement par chauffage de 352,59 à 422,39 degrés K (175
à 300 degrés F) pendant 1 à 30 heures.
REFERENCES CITED IN THE DESCRIPTION
This list of references cited by the applicant is for the reader's convenience only.
It does not form part of the European patent document. Even though great care has
been taken in compiling the references, errors or omissions cannot be excluded and
the EPO disclaims all liability in this regard.
Patent documents cited in the description