The invention relates to a heat-resistant Al—Cu—Mg—Ag alloy for producing semi-finished parts or products, suitable for use at rather high temperatures and with high static and dynamic strength properties combined with an improved creep resistance. The invention also relates to a process for producing a semi-finished part or product composed of such an aluminum alloy.
An alloy of the above-cited type is known in EP 1 518 000 B1 from which semi-finished parts are produced with high static and dynamic strength properties, and an improved creep resistance in comparison to previously-known, similar aluminum alloys. This alloy is registered with the Aluminum Association (AA) as alloy AA2016. This previously-known alloy already approximately unites the strength properties necessary for semi-finished parts and products that must resist high static and dynamic loads. These properties are known from the alloys AA2014, AA 2014A or AA2214 and have an improved creep resistance, which is an improved resistance under the action of temperature. The alloy AA2016 therefore satisfies the claims put on semi-finished parts and products produced from them that are exposed for a short time to elevated temperatures, for example as in the wheel halves of airplanes. These semi-finished products are exposed to elevated temperatures only during braking after the airplane sets down on the landing strip.
The alloys AA2618 and AA2618A are considered to be especially creep-resistant. However, semi-finished parts and products produced from these alloys have only relatively low static and dynamic strength values.
The alloys for producing semi-finished parts with high static and dynamic strength properties in accordance with AA2014, AA2014A and AA2214 differ chemically from the alloys with long-time thermal stability according to AA2618 and AA2618A. This is because the very strong aluminum alloys contain relatively high amounts of the elements silicon, copper and manganese and relatively low amounts of the elements magnesium and iron, whereas the long-time thermally stable aluminum alloys have a reduced amount of silicon, copper and manganese in contrast to the above and an elevated content of iron, nickel and magnesium. In addition, nickel is mixed into the long-time thermally stable alloys.
The alloy AA2016 differs from the previously described alloys in particular by an admixture of the element silver with amounts between 0.30 and 0.7 wt %. There are also differences in the remaining alloy elements in comparison to the composition of both the previously-cited very strong aluminum alloys, and the previously-cited aluminum alloys whose semi-finished parts have a good creep resistance.
Even if the aluminum alloy AA2016 is known to produce semi-finished parts and products that can satisfy high static and dynamic strength requirements and also resist elevated temperatures in short-time use, there has long been a desire to have available an aluminum alloy for producing semi-finished parts and products that resist elevated temperatures for longer-term use. Such requirements are placed on a plurality of products, for example, on the compressor wheels of a turbocharger in motor vehicle engine uses. These structural components must not only resist high static and dynamic loads, but also the high temperatures prevailing in such a use for the duration of the use. Similar requirements for long-time stability at rather high temperatures are also applicable to turbocharger compressors of large engines in ship construction.
The present invention provides an alloy from which a semi-finished part or a product can be produced that satisfies the desired properties for static and dynamic strength as well as long-time stability under high temperature.
This is accomplished by a heat-resistant Al—Cu—Mg—Ag alloy for producing semi-finished parts or products, suitable for use at rather high temperatures, with high static and dynamic properties of strength in combination with an improved creep resistance, containing:
0.3-0.7 wt % silicon (Si)
max. 0.15 wt % iron (Fe)
3.5-4.7 wt % copper (Cu)
0.05-0.5 wt % manganese (Mn)
0.3-0.9 wt % magnesium (Mg)
0.02-0.15 wt % titanium (Ti)
0.03-0.25 wt % zirconium (Zr)
0.1-0.7 wt % silver (Ag)
0.03-0.5 wt % scandium (Sc)
0.03-0.2 wt % vanadium (V)
max. 0.05 wt % others, individually
max. 0.15 wt % others, total
remainder aluminum.
This alloy has the elements scandium and vanadium in the cited amounts in particular. It is attributed to the interaction of these elements, together with the elements titanium and zirconium on the one hand and to the silver contained in the alloy on the other hand, that a semi-finished part produced from this alloy and accordingly the end product have sufficiently high static and dynamic strength properties as well as an especially good creep resistance. The strength properties may be slightly reduced in comparison to those of semi-finished parts from an aluminum alloy AA2016, but are clearly increased in comparison to such semi-finished parts produced from the alloy AA2618. These special properties of a semi-finished part produced from such an aluminum alloy were not to be expected. Therefore, this alloy is suitable for producing semi-finished parts and products that not only have to satisfy high static and dynamic strengths, but also must have a long-time stability under thermal influences, and therefore can have an excellent resistance to creep.
In one embodiment, the alloy contains 0.08 to 0.2 wt % scandium and 0.10 to 0.2 wt % vanadium. In another specification of this alloy composition, the aluminum alloy contains the electrodes titanium, zirconium, scandium and vanadium in the following amounts:
0.12 to 0.15 wt % titanium (Ti),
0.14 to 0.16 wt % zirconium (Zr),
0.13 to 0.17 wt % scandium (Sc) and
0.12 to 0.15 wt % vanadium (V).
Another improvement of the discussed properties of a semi-finished part or product produced from such an alloy can be achieved if the sum of the elements zirconium, titanium, scandium and vanadium is less than or equal to 0.4 wt %, and in particular less than or equal to 0.35 wt %.
The aluminum alloy preferably contains zirconium with amounts between 0.03 and 0.15 wt %. Titanium is preferably contained in the alloy with amounts between 0.03 and 0.09 wt %.
It is advantageous if the iron content of the alloy is limited to a max. of 0.09 wt %.
The special properties of the claimed Al—Cu—Mg—Ag alloy also appear if it has a reduced amount of dispersoid producers. This is present, for example, if the claimed alloy comprises the following amounts of the elements titanium, zirconium, scandium and vanadium:
0.04 to 0.06 wt % titanium (Ti),
0.05 to 0.07 wt % zirconium (Zr),
0.08 to 0.10 wt % scandium (Sc) and
0.10 to 0.12 wt % vanadium (V).
The aluminum alloy preferably contains 0.3 to 0.6 wt % silver.
Silicon preferably participates in the buildup of the alloy properties between 0.3 and 0.6 wt %.
The manganese content of the aluminum alloy is preferably set at 0.1 to 0.3 wt %.
Another improvement of the special static and dynamic strength properties as well as of the creep resistance can be achieved if the content of the elements silicon, copper, manganese, magnesium and silver of the aluminum alloy is limited as follows:
0.45-0.55 wt % silicon (Si)
4.10-4.30 wt % copper (Cu)
0.15-0.25 wt % manganese (Mn)
0.5-0.7 wt % magnesium (Mg) and
0.40-0.55 wt % silver (Ag).
Investigations have shown that the alloy, and the semi-finished parts or products produced from it, have an especially good creep resistance if the sum of the elements silver, zirconium, scandium and vanadium is at least 0.60 wt % and maximally 1.1 wt %.
It is advantageous if the elements silver and scandium are contained in the alloy in amounts such that the ratio of the amount of silver to scandium is between 5 and 23, and preferably between 9 and 14.
The amounts of the elements scandium and zirconium are advantageously contained in the alloy in a ratio of scandium to zirconium between 1 and 17, and preferably between 6 and 12.
In regard to amount of the elements silver and vanadium, a ratio of silver to vanadium between 0.5 and 14 is considered to be especially desirable, and in particular a ratio between 5 and 9.
Semi-finished parts or products are typically produced from the disclosed heat-resistant aluminum alloy by the following steps:
(a) Casting of a bar from the alloy with sufficient dissolution of the electrodes zirconium, scandium and vanadium,
(b) Homogenization of the cast bar at a temperature that is as close as possible below the melting temperature of the alloy for a time that is sufficient to achieve the most uniform distribution possible of the alloy elements in the cast structure, preferably at 485 to 510° C. for a period of 10 to 25 hour,
(c) Thermal deformation of the homogenized bar by extruding, forging (including reverse extrusion molding) and/or rolling in the temperature range of 280 to 470° C.,
(d) Solution annealing of the extruded, forged and/or rolled semi-finished part at temperatures that are high enough to bring the alloy elements necessary for the hardening into solution distributed in the structure, preferably at 480 to 510° C. over a time of 30 min to 8 h,
(e) Quenching the solution-annealed semi-finished part in water with a temperature between room temperature and 100° C. (boiling water) or in water-glycol mixtures with temperatures ≤50° C. and glycol contents of up to 60%,
(f) Selective cold deformation of the quenched semi-finished part by upsetting or stretching by an amount that results in a reduction of the intrinsic tensions produced during the quenching in cool quenching medium, preferably by 1-5%, and
(g) Thermal hardening of the semi-finished part quenched in this manner and selectively cold-upset or stretched at temperatures adapted to the planned usage, preferably between 80 and 210° C. over a time of 5 to 35 h, preferably 10 to 25 h in a 1-, 2- or 3-stage process.
A sufficient dissolution of the electrodes zirconium, scandium and vanadium can therefore be achieved by moving the melt during the melting of the alloy (i.e. the molten aluminium alloy) before the casting step and during the casting of a bar. It is especially advantageous if the melt is moved by convection. Such a convection can be produced by external magnetic influences, as for example in an induction furnace. Therefore, the aluminum alloy is preferably melted in an induction furnace.
The invention is described using exemplary embodiments and by comparison to previously known aluminum alloys, with reference made to the attached figures. In the figures:
The table of
Two typical alloy compositions of the claimed alloy were produced and investigated for the production of test pieces and for carrying out investigations of strength at room temperature and an elevated temperature. The two alloys W1 and W2 had the following chemical composition:
Furthermore, test pieces of the comparison alloys AA2016 and AA2618 were produced and correspondingly investigated. For the theoretical composition of these alloys, see the data in
In order to determine the strength properties, the alloys W1 and W2 were cast on an industrial scale to cast extrusion blocks with a diameter of 370 mm, whereby care was taken that the elements zirconium, scandium and vanadium were sufficiently dissolved during the casting of the bars. To this end, the molten aluminum alloy or melt was put in motion by generating a convection in the melt. The cast extrusion blocks were homogenized in order to compensate the crystal segregations conditioned by the hardening. The blocks were homogenized and cooled off in two stages using a temperature range of 500° C. to 550° C. After twisting off the casting skin, the homogenized blocks were preheated to approximately 400° C. and multiply deformed to free-form forged pieces with a thickness of 100 mm and a width of 250 mm. Subsequently, the free-form forged pieces from alloys W1 and W2 were solution-annealed for at least 2 h at 500° C., quenched in water, and subsequently hot-hardened between 165° C. and 200° C. Tensile tests were taken from the hot-hardened free-form forged pieces on which the strength properties were determined at room temperature in the longitudinal (L) test position. The results are listed in the table below:
For purposes of a comparison, the strength properties for free-form forged pieces of the alloys AA2016, followed by W1, W2 and AA2618 in the heat-hardened state are additionally indicated in the table.
The alloy AA2016 shows the greatest strength (stretch limit), followed by W1, W2 and AA2618. A sufficient ductility of >8% is achieved by all alloys. It should be noted at this point that the strength values of the comparison alloy AA2016 were not able to be reached with the test alloys W1, W2. However, the test values achieved clearly exceed those of the other comparison alloy AA2618. For the cases of use in question, the strength values that the test alloys W1, W2 have are sufficient. It is important that the test alloys W1, W2 have a significantly better creep resistance, as described in the following with reference to
The differences are especially noticeable in a comparison of the creep behavior of the alloy AA2618, known as creep-resistant, with the alloy W2. This comparison is shown in
The test pieces of the other test alloy W1 have a creep resistance that corresponds to the one shown in the diagram of
The special properties of the claimed alloy are also evident by a comparison of this alloy and of the two test alloys W1, W2 with known alloys in a Larsen-Miller diagram.
These curves of previously-known aluminum alloys are opposed by the area of the Larsen-Miller diagram in which the values of semi-finished parts or products produced with the claimed alloy are located. The line of the test pieces of the test alloys W1, W2 are concretely entered, whereby it is to be taken into consideration that this line does not represent the break line, but rather the state of the test samples after a test time of 500 hours. A break did not occur within this time frame (see also
Number | Date | Country | Kind |
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11177747 | Aug 2011 | EP | regional |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2012/064982 | 8/1/2012 | WO | 00 | 1/24/2014 |
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WO2013/023907 | 2/21/2013 | WO | A |
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