EP2516687B1 - Casting made from copper containing aluminium alloy with high mechanical strength and hot creep - Google Patents
Casting made from copper containing aluminium alloy with high mechanical strength and hot creep Download PDFInfo
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- EP2516687B1 EP2516687B1 EP10799072.3A EP10799072A EP2516687B1 EP 2516687 B1 EP2516687 B1 EP 2516687B1 EP 10799072 A EP10799072 A EP 10799072A EP 2516687 B1 EP2516687 B1 EP 2516687B1
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- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 title claims description 19
- 239000010949 copper Substances 0.000 title claims description 14
- 229910052802 copper Inorganic materials 0.000 title claims description 12
- 238000005266 casting Methods 0.000 title claims description 10
- 229910000838 Al alloy Inorganic materials 0.000 title claims description 9
- 229910045601 alloy Inorganic materials 0.000 claims description 60
- 239000000956 alloy Substances 0.000 claims description 60
- 239000011777 magnesium Substances 0.000 claims description 33
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 claims description 27
- 229910052749 magnesium Inorganic materials 0.000 claims description 25
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 claims description 14
- 229910052720 vanadium Inorganic materials 0.000 claims description 13
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 claims description 12
- 239000010936 titanium Substances 0.000 claims description 11
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 claims description 11
- 238000000034 method Methods 0.000 claims description 10
- 229910052719 titanium Inorganic materials 0.000 claims description 9
- 229910052726 zirconium Inorganic materials 0.000 claims description 9
- 229910052782 aluminium Inorganic materials 0.000 claims description 8
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 8
- QCWXUUIWCKQGHC-UHFFFAOYSA-N Zirconium Chemical compound [Zr] QCWXUUIWCKQGHC-UHFFFAOYSA-N 0.000 claims description 7
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 7
- 229910052759 nickel Inorganic materials 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 6
- 239000011701 zinc Substances 0.000 claims description 6
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 239000011572 manganese Substances 0.000 claims description 5
- 229910052710 silicon Inorganic materials 0.000 claims description 4
- 230000003068 static effect Effects 0.000 claims description 4
- 239000000126 substance Substances 0.000 claims description 4
- 229910052725 zinc Inorganic materials 0.000 claims description 4
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 claims description 3
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 claims description 3
- 229910052742 iron Inorganic materials 0.000 claims description 3
- 229910052748 manganese Inorganic materials 0.000 claims description 3
- 239000010703 silicon Substances 0.000 claims description 3
- 239000003232 water-soluble binding agent Substances 0.000 claims description 2
- 238000005507 spraying Methods 0.000 claims 1
- 240000008042 Zea mays Species 0.000 description 9
- CSDREXVUYHZDNP-UHFFFAOYSA-N alumanylidynesilicon Chemical compound [Al].[Si] CSDREXVUYHZDNP-UHFFFAOYSA-N 0.000 description 6
- 238000007711 solidification Methods 0.000 description 6
- 230000008023 solidification Effects 0.000 description 6
- 229910000676 Si alloy Inorganic materials 0.000 description 5
- 238000002679 ablation Methods 0.000 description 4
- JRBRVDCKNXZZGH-UHFFFAOYSA-N alumane;copper Chemical compound [AlH3].[Cu] JRBRVDCKNXZZGH-UHFFFAOYSA-N 0.000 description 4
- 239000012535 impurity Substances 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000000465 moulding Methods 0.000 description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 230000007423 decrease Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 238000010791 quenching Methods 0.000 description 3
- 230000000171 quenching effect Effects 0.000 description 3
- 230000002829 reductive effect Effects 0.000 description 3
- 238000007528 sand casting Methods 0.000 description 3
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 229940082150 encore Drugs 0.000 description 2
- 230000002349 favourable effect Effects 0.000 description 2
- 230000000670 limiting effect Effects 0.000 description 2
- 238000004064 recycling Methods 0.000 description 2
- 238000007670 refining Methods 0.000 description 2
- 230000000717 retained effect Effects 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 229910003407 AlSi10Mg Inorganic materials 0.000 description 1
- 229910000789 Aluminium-silicon alloy Inorganic materials 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- 229910000881 Cu alloy Inorganic materials 0.000 description 1
- 241000251948 Dolophilodes major Species 0.000 description 1
- 241001644893 Entandrophragma utile Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000004411 aluminium Substances 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052786 argon Inorganic materials 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- 238000009749 continuous casting Methods 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000284 extract Substances 0.000 description 1
- 229910002804 graphite Inorganic materials 0.000 description 1
- 239000010439 graphite Substances 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000005457 optimization Methods 0.000 description 1
- 239000008188 pellet Substances 0.000 description 1
- 230000000750 progressive effect Effects 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000010112 shell-mould casting Methods 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 238000005496 tempering Methods 0.000 description 1
- 238000009864 tensile test Methods 0.000 description 1
Images
Classifications
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/12—Alloys based on aluminium with copper as the next major constituent
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D21/00—Casting non-ferrous metals or metallic compounds so far as their metallurgical properties are of importance for the casting procedure; Selection of compositions therefor
- B22D21/002—Castings of light metals
- B22D21/007—Castings of light metals with low melting point, e.g. Al 659 degrees C, Mg 650 degrees C
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/12—Alloys based on aluminium with copper as the next major constituent
- C22C21/14—Alloys based on aluminium with copper as the next major constituent with silicon
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C21/00—Alloys based on aluminium
- C22C21/12—Alloys based on aluminium with copper as the next major constituent
- C22C21/16—Alloys based on aluminium with copper as the next major constituent with magnesium
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22F—CHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
- C22F1/00—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
- C22F1/04—Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
- C22F1/057—Changing 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 copper as the next major constituent
Definitions
- the invention relates to copper aluminum alloy castings subjected to high mechanical stresses and working, at least in some of their areas, at high temperatures, including cylinder heads supercharged diesel or gasoline engines.
- the alloys commonly used for the cylinder heads of automotive mass-produced vehicles are essentially silicon alloys (5 to 10% Si in general) often containing copper and magnesium in order to increase their mechanical characteristics, especially when hot. .
- the main types used are as follows: AlSi7Mg, AlSi7CuMg, AlSi (5 to 8) Cu3Mg, AlSi10Mg, AlSi10CuMg.
- These alloys are used with different methods of heat treatment: sometimes in the F-state without any treatment, sometimes in the T5 state with a simple income, sometimes in the T6 state with dissolution, quenching and drying. at the peak of hardening or slightly below, and often in the T7 state with dissolution, quenching and over-tempering or stabilization.
- copper alloys of the AlCu5 type are also sometimes used. added with elements promoting the heat resistance such as Ni, Co, Ti, V and Zr: there is particularly in this category AlCu5NiCoZr and AlCu4NiTi. These alloys are very resistant to heat, especially at 300 ° C where they clearly outperform the silicon aluminum mentioned above, but suffer from two serious weaknesses: their high cracks, combined with a bad shrinkage behavior, which makes them very difficult.
- Table 1 summarizes the characteristics at ambient temperature of these two sand-cast alloys heat-treated in the T7 state (Rp0.2 (or 0.2% TYS) being the elastic limit in MPa; Rm (or UTS) being the breaking strength in MPa, and A (or E) being elongation at break in%: Table 1 Alloy Rp0.2 (MPa) Rm (MPa) AT (%) AlCu4NiTi Unmeasurable 343 0.11 AlCu5NiCoZr 270 295 1
- AlCu5Mg alloys such as AlCu5MgTi (designated as 204 AA), and A206 and B206 (AA), for room temperature or moderate working parts do not meet these requirements, particularly 300 ° C.
- the alloys AlCu4NiTi and AlCu5NiCoZr (203 following AA) mentioned above are too weak and fragile at room temperature.
- the invention is based on the finding by the applicant that it is possible to make very significant improvements to the characteristics mentioned above of the old alloy 224 (according to the AA), and thus to solve the problem posed, in particular by the addition of a limited amount of magnesium.
- the addition of a small amount of magnesium, of the order of 0.10 to 0.15%, makes it possible to considerably increase the yield strength and the resistance of the alloy not only at room temperature but also hot, especially at 250-300 ° C and above. It is at room temperature that the relative gain is the most important: as explained in the following examples and Tables 6, 7, 8, the elastic limit goes from about 190 MPa without magnesium to about 340 MPa with only 0.09% and then at over 390 MPa with 0.13%. If we consider the average results obtained with 0.09% and 0.13% magnesium, the gains observed on the yield strength and the resistance at ambient temperature are remarkable: respectively + 96% and + 29% in relative terms.
- the elongation is substantially reduced by half but still retains a suitable level of 6 to 8%.
- the gains brought by the addition of magnesium remain even if they decrease.
- the observed gains in yield strength and strength are respectively 35 and 13% in relative terms at 250 ° C, and 27 and 8% in relative terms at 300 ° C.
- the addition of magnesium remains beneficial at least up to 300 ° C., especially as the loss of elongation fades at these high temperatures.
- the addition of magnesium considerably improves the hot creep resistance, reducing by approximately 2, for example, the deformation observed after 300 h at 300 ° C. under a stress of 30 MPa.
- the addition of magnesium therefore does not affect the hot stability, contrary to the philosophy that led to the definition of alloys AlCu5NiCoZr (203 following the AA) and AlCu5MnVZr (224 following the AA) conventional that are devoid of magnesium .
- the alloy according to the invention treated T7 can be compared with the AlSi7Cu3.5Mg0.15MnVZrTi also treated T7, which was also developed by the applicant and is its most creep-resistant knowledge of the series of aluminum silicon alloys considered in the previous table.
- the curve of the figure 3 shows the very great superiority of the AlCu4.7MnMgVZrTi, which deforms substantially 4 times less under the same conditions.
- the magnesium content can be increased beyond the area already experienced in the examples. If only very high strength and hardness are sought, with a reduced ductility requirement, a maximum level of 0.38% can be envisaged, knowing that the burn temperature will be lowered and the heat treatment will have to be adapted. The minimum to obtain a significant curing effect is of the order of 0.05%. A smaller range is from 0.07% to 0.30% and the preferred range, corresponding to the resistance-ductility-creep tradeoffs quantified in the examples while having an industrially acceptable width is 0.08-0.20%, or even 0.09-1.03%.
- the other elements are to be considered as impurities.
- Table 4 A series of three alloy compositions described in Table 4 was developed in a 35 kg electric furnace, all elements being expressed in% by weight.
- Table 4 landmark Yes Fe Cu mn mg Ti V Zr 0 Mg 0.09 0.14 4.83 0.34 0.00 0.18 0.21 0.14 0.09 Mg 0.08 0.14 4.74 0.33 0.09 0.22 0.17 0.13 0.13 Mg 0.09 0.14 4.81 0.33 0.13 0.20 0.17 0.13
- FIG. figure 1 Du "(6.5 mm) diameter shell specimens of the Rio Tinto Alcan type, represented in FIG. figure 1 for tensile tests and ASTM B108 1 ⁇ 2 "(12.7 mm) shell test pieces to be used as blanks for 4 mm diameter creep specimens.
- figure 1 is more particularly a cluster 10 of 4 test tubes 11 of Rio Tinto Alcan cast into shell with a diameter of the barrel 1 ⁇ 4 "(6.35 mm) .This cluster 10 takes, scale 1/2, the design of the ASTM specimen B108.
- the burning temperature of the various compositions was first determined by performing differential enthalpic analyzes (AED) on pellets machined in the cast specimens. The rate of rise in temperature was 20 ° C / minute. The AED curves are represented at figure 2 . The burn temperatures observed corresponding to the melting peaks obviously depend on the magnesium content as shown in Table 5: Table 5 Content in Mg (%) Burning temperature (° C) 0 542.7 0.09 538.2 0.13 533.9
- the burn temperature gradually shifts to lower temperatures when the Mg content increases from 0% to 0.09% and then to 0.13%.
- the blanks intended for the creep tests were subjected, prior to this heat treatment, to hot isostatic compaction at 1000 bar at 485 ° C. for 2 hours in order to eliminate any microporosity which could seriously affect the tests given the small diameter of the specimen.
- Static mechanical characteristics were measured at room temperature and at 250 ° C and 300 ° C. In the latter two cases, the specimens were preheated for 100 hours at the temperature before being tracted.
- Table 6 Mechanical characteristics at room temperature Alloy Rp0.2 rm AT Mg (%) MPa MPa % 0 187.8 349.3 15.3 0.09 344.5 435.0 8.2 0.13 393.4 466.4 6.6 Alloy Rp0.2 rm AT Mg (%) MPa MPa % 0 134.7 199.5 10.7 0.09 172.2 223.7 7.3 0.13 191.4 228.8 12.2 Alloy Rp0.2 rm AT Mg (%) MPa MPa % 0 98.3 147.1 14.5 0.09 130.2 167.2 11.2 0.13 120.0 149.4 18.3
- Table 9 summarizes the results: Table 9: Creep at 300 ° C. under 30 MPa Magnesium content (%) Deformation (in%) after 300h 0 0.26 0.09 0.13 0.13 0.14
- a part may then be molded from the advantageous alloy defined above, this part may in particular be a cylinder head or an insert of a cylinder head or of another part requiring a high static mechanical resistance at room temperature and at room temperature. hot and high resistance to creep when hot, in particular at 300 ° C.
- the part is advantageously treated T7, even if a T6 treatment is also possible.
- Ablation molding is particularly suitable for molding high-tread alloys. Initially, it is sand casting that does not much upset the withdrawal, and then after removal of the mold the end of the solidification is carried out without rigid mold at all. In addition to providing a high solidification rate, the process also leads to high temperature gradients because the spray is generally progressive, starting on selected areas and advancing towards the end points of solidification where it is possible to attach. the weights. This advantageously also favors the use of alloys with low feed capacity of the shrink, such as copper aluminum alloys, including the alloy according to the invention.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Materials Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Cylinder Crankcases Of Internal Combustion Engines (AREA)
- Supercharger (AREA)
Description
L'invention concerne les pièces moulées en alliage d'aluminium au cuivre soumises à des contraintes mécaniques élevées et travaillant, au moins dans certaines de leurs zones, à des températures élevées, notamment des culasses de moteurs diesel ou essence suralimentés.The invention relates to copper aluminum alloy castings subjected to high mechanical stresses and working, at least in some of their areas, at high temperatures, including cylinder heads supercharged diesel or gasoline engines.
Sauf mention contraire, toutes les valeurs relatives à la composition chimique des alliages sont exprimées en pourcentages pondéraux.Unless stated otherwise, all the values relating to the chemical composition of the alloys are expressed in percentages by weight.
Les alliages couramment utilisés pour les culasses des véhicules de grande série automobile sont essentiellement des alliages au silicium (de 5 à 10 % de Si en général) contenant souvent du cuivre et du magnésium afin d'en augmenter les caractéristiques mécaniques, en particulier à chaud. Les principaux types utilisés sont les suivants : AlSi7Mg, AlSi7CuMg, AlSi(5 à 8)Cu3Mg, AlSi10Mg, AlSi10CuMg. Ces alliages sont utilisés avec différentes modalités de traitements thermiques : parfois à l'état état F sans aucun traitement, parfois à l'état état T5 avec un simple revenu, parfois à l'état T6 avec une mise en solution, une trempe et un revenu au pic de durcissement ou légèrement en-dessous, et souvent à l'état T7 avec une mise en solution, une trempe et un sur-revenu ou une stabilisation.The alloys commonly used for the cylinder heads of automotive mass-produced vehicles are essentially silicon alloys (5 to 10% Si in general) often containing copper and magnesium in order to increase their mechanical characteristics, especially when hot. . The main types used are as follows: AlSi7Mg, AlSi7CuMg, AlSi (5 to 8) Cu3Mg, AlSi10Mg, AlSi10CuMg. These alloys are used with different methods of heat treatment: sometimes in the F-state without any treatment, sometimes in the T5 state with a simple income, sometimes in the T6 state with dissolution, quenching and drying. at the peak of hardening or slightly below, and often in the T7 state with dissolution, quenching and over-tempering or stabilization.
La raison pour laquelle on utilise des alliages aluminium silicium est la supériorité de leurs propriétés de fonderie, en particulier absence de criquabilité, coulabilité élevée, bon pouvoir d'alimentation de la retassure. Seuls ces alliages à silicium supérieur ou égal à 5% se prêtent bien au moulage en coquille, par gravité ou basse pression, qui est le procédé dominant pour les culasses automobiles de grande série.The reason for using aluminum silicon alloys is the superiority of their foundry properties, in particular lack of creasability, high flowability, good power of the shrink. Only these silicon alloys greater than or equal to 5% lend themselves to shell molding, by gravity or low pressure, which is the dominant process for large series cylinder heads.
Pour des fabrications de faible série généralement faites en moulage au sable, telles que les culasses de véhicules à hautes performances ou les pièces travaillant à chaud destinées à l'armement et à l'aéronautique, on utilise aussi parfois des alliages au cuivre du type AlCu5 additionnés d'éléments favorisant la tenue à chaud comme Ni, Co, Ti, V et Zr : on note en particulier dans cette catégorie l'AlCu5NiCoZr et l'AlCu4NiTi. Ces alliages sont très résistants à chaud, en particulier à 300°C où ils surpassent nettement les aluminium silicium mentionnés plus haut, mais souffrent de deux graves faiblesses : leur criquabilité élevée, joint à un mauvais comportement à la retassure, qui les rend très difficiles à couler en coquille en grande série, et également la médiocrité de leurs caractéristiques mécaniques à température ambiante : ils ont en particulier un allongement très faible, qui les rend fragiles et peu performants en fatigue mécanique. Le tableau 1 résume les caractéristiques à température ambiante de ces deux alliages coulés au sable et traitées thermiquement à l'état T7 (Rp0.2 (ou 0.2%TYS) étant la limite d'élasticité en MPa ; Rm (ou UTS) étant la résistance à la rupture en MPa ; et A (ou E) étant l'allongement à la rupture en %):
Il existe aussi un alliage anciennement normalisé par l'Aluminum Association (désignée « AA » par la suite par commodité) sous le numéro 224, qui est du type AlCu5Mn VZr. Il a été déclaré « inactif » par cette association qui l'a retiré depuis des années de son document périodiquement remis à jour « Désignations and Chemical Composition Limits for Aluminum Alloys in the Form of Castings and Ingot ». Cet alliage 224 ne contient pas de magnésium (cet élément entrant dans la catégorie des impuretés, avec un maximum à 0.03% chacune, 0.10% total), et des résultats de caractérisation anciens sur des plaques coulées au sable ont montré les caractéristiques à l'état T7 décrites dans le tableau 2 :
Etant donné que, dans les futurs moteurs diesel à rampe commune ou suralimentés à essence, les chambres de combustion des culasses, et en particulier les pontets inter-soupapes, atteindront, voire dépasseront, 300°C, et subiront des pressions plus élevées que dans les générations des moteurs précédents aujourd'hui en service, l'emploi d'alliages aluminium cuivre constitue une solution « en rupture » par rapport aux progrès incrémentaux apportés par l'optimisation des alliages aluminium silicium.Since, in future common-rail or gas-supercharged diesel engines, the cylinder head combustion chambers, and in particular the inter-valve bridges, will reach or exceed 300 ° C and will experience higher pressures than in generations of previous engines in use today, the use of copper aluminum alloys is a solution "break" compared to the incremental progress made by the optimization of silicon aluminum alloys.
Mais il faut encore trouver un alliage de cette famille qui combine :
- hautes propriétés mécaniques à température ambiante,
- hautes propriétés mécaniques dans le domaine 250 - 300°C,
- et haute résistance au fluage à 300°C, température caractéristique notamment des pontets inter-soupapes, éléments particulièrement sollicités thermo-mécaniquement.
- high mechanical properties at room temperature,
- high mechanical properties in the range 250 - 300 ° C,
- and high resistance to creep at 300 ° C, characteristic temperature including inter-valve bridges, particularly thermomechanically stressed elements.
Les alliages AlCu5Mg classiques tels que l'AlCu5MgTi (désigné 204 suivant l'AA), et les A206 et B206 (suivant l'AA), destinés à des pièces travaillant à température ambiante ou modérée ne répondent pas à ces exigences, en particulier à 300°C.Conventional AlCu5Mg alloys such as AlCu5MgTi (designated as 204 AA), and A206 and B206 (AA), for room temperature or moderate working parts do not meet these requirements, particularly 300 ° C.
Les alliages AlCu4NiTi et AlCu5NiCoZr (203 suivant l'AA) mentionnés plus haut sont eux trop faibles et fragiles à température ambiante.The alloys AlCu4NiTi and AlCu5NiCoZr (203 following AA) mentioned above are too weak and fragile at room temperature.
L'AlCu5MnVZr (ancien 224 suivant l'AA) destiné aux pièces travaillant à chaud présente une combinaison de propriétés plus intéressante mais manque encore de limite d'élasticité à température ambiante par rapport aux propriétés améliorées recherchées: il donne, à l'état T7, une limite d'élasticité Rp0.2 = 280 MPa, à comparer avec 275 MPa pour l'AlSi7Cu0.5Mg0.3 T7 et 311 MPa pour l'AlSi5Cu3Mg T7 (valeurs mesurées par la demanderesse et publiées respectivement dans les articles « Alliages d'aluminium améliorés pour culasses Diesel » (Hommes et fonderie- février 2008- N° 382) et « Aluminium Casting Alloys for Highly Stressed Diesel Cylinder Heads », (3. internationales Symposium Aluminium + Automobil) ;Düsseldorf ; FRG; 3-4 Feb.1988, pp. 154 - 159, 1988).The AlCu5MnVZr (formerly 224 following AA) for hot workpieces has a more interesting combination of properties but still lacks yield strength at room temperature compared to the desired improved properties: it gives, in state T7 , a yield strength Rp0.2 = 280 MPa, compared with 275 MPa for AlSi7Cu0.5Mg0.3 T7 and 311 MPa for AlSi5Cu3Mg T7 (values measured by the applicant and published respectively in the articles "alloys of 'Enhanced Aluminum for Diesel Cylinders' (Men and Foundry - February 2008- No. 382) and 'Aluminum Casting Alloys for Highly Stressed Diesel Cylinder Heads', (3. International Symposium Aluminum + Automobil); Düsseldorf; FRG; 3-4 Feb 1988, pp. 154-159, 1988).
On a donc cherché à obtenir un progrès considérable par rapport à l'ancien 224 en termes de limite d'élasticité et de résistance ultime depuis la température ambiante jusqu'à 250 - 300°C. On a aussi cherché à améliorer la résistance au fluage à 300°C de cet ancien alliage.It has therefore been sought to achieve considerable progress with respect to the former 224 in terms of yield strength and ultimate strength from ambient temperature to 250 - 300 ° C. It has also been sought to improve the creep resistance at 300 ° C. of this old alloy.
L'invention a donc pour objet une pièce moulée à haute résistance mécanique statique à la température ambiante et à chaud et à haute tenue au fluage à chaud, en particulier à 300°C et plus, coulée en alliage d'aluminium de composition chimique suivante, exprimée en pourcentages pondéraux :
- Si : 0.02 - 0.50 %, de préférence 0.02 - 0.20 % et plus préférentiellement 0.02 - 0.06%,
- Fe : 0.02 - 0.30 %, de préférence 0.02 -0.20 %, plus préférentiellement 0.02 - 0.12 % et mieux 0.02 - 0.06%,
- Cu : 3.5 - 4.9 %, de préférence 3.8 - 4.9 % et plus préférentiellement 4.0 - 4.8 %,
- Mn : < 0.70 %, de préférence 0.20 - 0.50 %,
- Mg : 0.05 - 0.20 %, de préférence 0.07 - 0.20 %, et plus préférentiellement 0.08 - 0.20 % et enfin de façon très préférentielle 0.09 - 0.13%,
- Zn : < 0.30 %, de préférence < 0.10 % et plus préférentiellement < 0.03%,
- Ni : < 0.30 %, de préférence < 0.10 % et plus préférentiellement < 0.03%,
- V : 0.05 - 0.30 %, de préférence 0.08 - 0.25 %, et plus préférentiellement 0.10 - 0.20%,
- Zr : 0.05 - 0.25 %, de préférence 0.08 - 0.20 %,
- Ti : 0.01 - 0.35 %, de préférence 0.05 - 0.25 % et plus préférentiellement 0.10 - 0.20%, autres éléments au total < 0.15%; et 0.05 % chacun,
- reste aluminium.
- If: 0.02 - 0.50%, preferably 0.02 - 0.20% and more preferably 0.02 - 0.06%,
- Fe: 0.02 - 0.30%, preferably 0.02 -0.20%, more preferably 0.02 - 0.12% and better 0.02 - 0.06%,
- Cu: 3.5 - 4.9%, preferably 3.8 - 4.9% and more preferably 4.0 - 4.8%,
- Mn: <0.70%, preferably 0.20 - 0.50%,
- Mg: 0.05 - 0.20%, preferably 0.07 - 0.20%, and more preferably 0.08 - 0.20% and finally very preferably 0.09 - 0.13%,
- Zn: <0.30%, preferably <0.10% and more preferably <0.03%,
- Ni: <0.30%, preferably <0.10% and more preferably <0.03%,
- V: 0.05 - 0.30%, preferably 0.08 - 0.25%, and more preferably 0.10 - 0.20%,
- Zr: 0.05 - 0.25%, preferably 0.08 - 0.20%,
- Ti: 0.01 - 0.35%, preferably 0.05 - 0.25% and more preferably 0.10 - 0.20%, other elements total <0.15%; and 0.05% each,
- remains aluminum.
-
La
figure 1 représente une grappe de quatre éprouvettes coulées en coquille de la société Rio Tinto Alcan de diamètre ¼" (6.35 mm).Thefigure 1 represents a cluster of four shell cast specimens from the Rio Tinto Alcan company with a diameter of ¼ "(6.35 mm). -
La
figure 2 représente des courbes d'analyse enthalpique différentielle pour les alliages AlCu4.7MnVZrTi à teneur en magnésium de 0%, 0.09% et 0.13%.Thefigure 2 represents differential enthalpy analysis curves for AlCu4.7MnVZrTi alloys with magnesium content of 0%, 0.09% and 0.13%. -
La
figure 3 montre des résultats d'essais de fluage à 300°C sur les alliages AlCu4.7MnVZrTi traités T7 et AlSi7Cu3.5MnVZrTi également traité T7 à teneur en magnésium variable respectivement de 0% à 0.13%.et de 0.1 % à 0.15%.Thefigure 3 shows results of creep tests at 300 ° C on T7-treated AlCu4.7MnVZrTi and AlSi7Cu3.5MnVZrTi alloys also treated T7 with variable magnesium content respectively from 0% to 0.13% and from 0.1% to 0.15%.
L'invention repose sur la constatation par la demanderesse qu'il est possible d'apporter de très importantes améliorations aux caractéristiques citées plus haut de l'ancien alliage 224 (suivant l'AA), et de résoudre ainsi le problème posé, ce notamment par l'addition d'une quantité limitée de magnésium.The invention is based on the finding by the applicant that it is possible to make very significant improvements to the characteristics mentioned above of the old alloy 224 (according to the AA), and thus to solve the problem posed, in particular by the addition of a limited amount of magnesium.
En effet, l'addition d'une petite quantité de magnésium, de l'ordre de 0.10 à 0.15%, permet d'augmenter de façon considérable la limite d'élasticité et la résistance de l'alliage non seulement à température ambiante mais aussi à chaud, en particulier à 250-300°C et plus. C'est à température ambiante que le gain relatif est le plus important : comme exposé dans les exemples qui suivent et les tableaux 6, 7, 8, la limite d'élasticité passe d'environ 190 MPa sans magnésium à environ 340 MPa avec seulement 0.09% et ensuite à plus de 390 MPa avec 0.13%. Si l'on considère la moyenne des résultats obtenus avec 0.09% et 0.13% de magnésium, les gains observés sur la limite d'élasticité et la résistance à température ambiante sont remarquables : respectivement + 96% et + 29% en termes relatifs.Indeed, the addition of a small amount of magnesium, of the order of 0.10 to 0.15%, makes it possible to considerably increase the yield strength and the resistance of the alloy not only at room temperature but also hot, especially at 250-300 ° C and above. It is at room temperature that the relative gain is the most important: as explained in the following examples and Tables 6, 7, 8, the elastic limit goes from about 190 MPa without magnesium to about 340 MPa with only 0.09% and then at over 390 MPa with 0.13%. If we consider the average results obtained with 0.09% and 0.13% magnesium, the gains observed on the yield strength and the resistance at ambient temperature are remarkable: respectively + 96% and + 29% in relative terms.
L'allongement est par contre sensiblement réduit de moitié mais conserve encore un niveau convenable de 6 à 8%.However, the elongation is substantially reduced by half but still retains a suitable level of 6 to 8%.
A température élevée, 250 puis 300°C, les gains apportés par l'ajout de magnésium subsistent même s'ils diminuent. Les gains observés sur la limite d'élasticité et la résistance sont respectivement de 35 et 13% en termes relatifs à 250°C, et de 27 et 8% en termes relatifs à 300°C. Loin de nuire à la stabilité à chaud des phases durcissantes comme on aurait pu l'envisager, l'addition de magnésium reste bénéfique au moins jusqu'à 300°C, et ce d'autant que la perte d'allongement s'estompe à ces températures élevées.At high temperature, 250 then 300 ° C, the gains brought by the addition of magnesium remain even if they decrease. The observed gains in yield strength and strength are respectively 35 and 13% in relative terms at 250 ° C, and 27 and 8% in relative terms at 300 ° C. Far from impairing the hot stability of the hardening phases as might have been envisaged, the addition of magnesium remains beneficial at least up to 300 ° C., especially as the loss of elongation fades at these high temperatures.
De plus, l'addition de magnésium améliore considérablement la tenue au fluage à chaud, réduisant par approximativement 2 par exemple la déformation observée après 300h à 300°C sous une contrainte de 30 MPa. L'addition de magnésium ne nuit donc pas à la stabilité à chaud, contrairement à la philosophie qui a conduit à la définition des alliages AlCu5NiCoZr (203 suivant l'AA) et AlCu5MnVZr (224 suivant l'AA) classiques qui sont dépourvus de magnésium.In addition, the addition of magnesium considerably improves the hot creep resistance, reducing by approximately 2, for example, the deformation observed after 300 h at 300 ° C. under a stress of 30 MPa. The addition of magnesium therefore does not affect the hot stability, contrary to the philosophy that led to the definition of alloys AlCu5NiCoZr (203 following the AA) and AlCu5MnVZr (224 following the AA) conventional that are devoid of magnesium .
Il est intéressant de situer le niveau moyen de performance de l'alliage suivant l'invention (par souci de simplicité on a attribué la moyenne des caractéristiques des alliages à 0.09% et 0.13% de magnésium à l'alliage désigné « AlCu4.7MnMgmoyVZrTi ») comparativement à quelques alliages culasses à base aluminium-silicium. Le tableau 3 résume les caractéristiques mécaniques.
En ce qui concerne la tenue au fluage à 300°C, l'alliage selon l'invention traité T7 peut être comparé à l'AlSi7Cu3.5Mg0.15MnVZrTi également traité T7, qui a aussi été mis au point par la demanderesse et est à sa connaissance le plus résistant au fluage de la série d'alliages aluminium silicium considérés dans le tableau précédent. La courbe de la
Il apparaît ainsi que l'objectif de progrès « en rupture » par rapport aux alliages existants est bien atteint par l'addition de magnésium à une base de type AlCu5MnVZrTi.It thus appears that the objective of "breaking" progress with respect to existing alloys is achieved by the addition of magnesium to a base of AlCu5MnVZrTi type.
Bien que l'addition de magnésium abaisse progressivement la température de brûlure hors équilibre, il reste possible de mettre en solution l'alliage à 525°C ou 528°C comme on le fait par exemple assez classiquement avec les alliages A206 et B206. Un traitement par palier permettra éventuellement de traiter l'alliage à une température finale un peu plus haute mais ce traitement par palier n'est pas indispensable compte tenu des résultats très élevés obtenus avec un traitement isotherme sous la température de brûlure.Although the addition of magnesium gradually lowers the off-equilibrium burn temperature, it is still possible to dissolve the alloy at 525 ° C. or 528 ° C., as is done, for example, with conventional alloys A206 and B206. A step treatment will eventually allow the alloy to be processed at a slightly higher final temperature, but this stepwise treatment is not essential, given the very high results achieved with isothermal treatment under the burn temperature.
La teneur en magnésium peut être augmentée au-delà du domaine déjà expérimenté dans les exemples. Si on recherche uniquement résistance et dureté très élevées, avec une exigence de ductilité réduite, un niveau maximum de 0.38% peut être envisagé, sachant que la température de brûlure en sera abaissée et le traitement thermique devra être adapté. Le minimum pour obtenir un effet durcissant significatif est de l'ordre de 0.05%. Un domaine plus restreint est de 0.07% à 0.30% et le domaine préféré, correspondant aux compromis résistance - ductilité - fluage quantifié dans les exemples tout en ayant une largeur industriellement acceptable est 0.08 - 0.20%, voire de 0.09 à 0.13%.The magnesium content can be increased beyond the area already experienced in the examples. If only very high strength and hardness are sought, with a reduced ductility requirement, a maximum level of 0.38% can be envisaged, knowing that the burn temperature will be lowered and the heat treatment will have to be adapted. The minimum to obtain a significant curing effect is of the order of 0.05%. A smaller range is from 0.07% to 0.30% and the preferred range, corresponding to the resistance-ductility-creep tradeoffs quantified in the examples while having an industrially acceptable width is 0.08-0.20%, or even 0.09-1.03%.
Pour ce qui concerne les autres éléments constitutifs du type d'alliage suivant l'invention, leurs teneurs sont justifiées par les considérations suivantes :
- Silicium : il est généralement néfaste à la ductilité et peut abaisser la température de brûlure. Par contre, il améliore les propriétés de fonderie et en particulier est susceptible, même à faible niveau, de réduire la criquabilité, comme décrit dans l'
ASM Handbook, volume 15, édition 2008 - Fer : il est néfaste à la ductilité, mais diminue par contre la criquabilité, comme également décrit dans l'
ASM Handbook, volume 15, édition 2008 - Cuivre : il durcit l'alliage, augmentant limite d'élasticité et résistance mais diminuant l'allongement. La fourchette de l'ancien alliage 224 était de 4.5 à 5.5%. L'expérience acquise par la demanderesse avec le B206 indique qu'il est bon de limiter le cuivre à un maximum de 4.9% car au-delà il est très difficile de remettre tout le cuivre en solution. Comme les présents résultats, obtenus avec un cuivre de 4.7 à 4.8%, montrent que la résistance à température ambiante obtenue avec addition de magnésium est très élevée mais que l'allongement est réduit par rapport à l'ancien alliage 224 sans magnésium, il est logique de prévoir la possibilité de réduire le cuivre en dessous de 4.5%, et plus particulièrement jusqu'à 3,5%. La demanderesse a effectué des travaux sur l'alliage B206 pour lesquels elle estime que les résultats qui sont transposables à l'alliage selon l'invention et montrent que qu'un abaissement du cuivre de 5.0% à 4.0% permet de gagner notablement en allongement au prix d'une perte de résistance, mais que celle-ci reste supérieure à 400 MPa. Dans l'optique de certaines culasses, il est même concevable d'accepter une baisse un peu plus importante de la résistance pour privilégier l'allongement et de réduire le cuivre jusqu'à 3.5%. On pourra choisir des sous-domaines entre 3.5% et 4.9% en fonction du compromis de caractéristiques visées pour la pièce spécifique. D'une façon générale, des sous domaines centrés sur 4.3% ou 4.4% tels que 3.8 - 4.9% et mieux 4.0 - 4.8% conduisent à un compromis assez équilibré.
- Manganèse: cet élément ne doit pas excéder 0.70% sous peine de risquer de former des phases intermétalliques grossières. Comme il améliore généralement les propriétés mécaniques, particulièrement à chaud, un domaine de 0.20 - 0.50% analogue à celui des alliages du type 206 est préféré.
- Zinc: cet élément est une impureté qui, à haute teneur, peut diminuer les propriétés mécaniques et rendre le bain liquide plus oxydable. On peut envisager de tolérer jusqu'à 0.30% dans le but de faciliter l'emploi de métal de recyclage, mais on préfère moins de 0.10% et mieux moins de 0.03% pour des pièces à hautes performances.
- Nickel: il contribue en général à la résistance mécanique à chaud mais réduit considérablement l'allongement. Comme la résistance à chaud est assurée dans l'invention par l'addition d'autres éléments, cuivre, magnésium, vanadium et zirconium, le nickel est considéré ici comme une impureté, qu'on limite au maximum à 0.30% dans le but de faciliter l'emploi de métal de recyclage, et de préférence à 0.10% et encore mieux à 0.03% pour des pièces à hautes performances.
- Vanadium: Cet élément péritectique améliore en particulier la résistance au fluage à chaud. La demanderesse a observé que, dans une autre base d'alliage contenant du silicium, la résistance au fluage était fortement améliorée entre 0 et 0.05%, puis s'améliorait ensuite plus progressivement de 0.05% à 0.17% et était au-dessus de 0.17% stable à un excellent niveau. Limiter le niveau maximum de vanadium à 0.15% comme dans l'ancien 224 ne paraît donc pas souhaitable. Dans l'alliage suivant l'invention, un niveau de 0.05 à 0.30% est prévu, qui pourra être resserré à des sous-domaines plus étroits de 0.08 - 0.25% et préférentiellement 0.10 - 0.20%.
- Zirconium: cet élément péritectique améliore également en particulier la résistance au fluage à chaud, et son effet est additif à celui du vanadium. Une teneur de 0.05 - 0.25% et de préférence 0.08 - 0.20% est retenue.
- Titane: cet élément péritectique a deux effets différents : d'une part, il est souvent utilisé comme élément affinant du grain, souvent en combinaison avec un ajout d'alliage mère ou de sel ajoutant du titane et du bore. Cependant, il existe d'autres pratiques d'affinage consistant à n'ajouter que des produits introduisant du titane et du bore, voire même du bore seul, et dans ce dernier cas la présence de titane n'est pas favorable. D'autre part, le titane contribue à la bonne résistance au fluage à chaud, quoi que moins fortement que vanadium et zirconium, comme la demanderesse l'a observé. On a donc retenu une teneur maximum de 0.35%, mais on préférera en général une addition de 0.05 à 0.25% et encore mieux de 0.10 à 0.20%.
- Silicon: It is generally harmful to ductility and can lower the burn temperature. On the other hand, it improves the casting properties and in particular is capable, even at a low level, of reducing the creasability, as described in FIG.
ASM Handbook, volume 15, edition 2008 - Iron: it is harmful to the ductility, but decreases against the crackability, as also described in the
ASM Handbook, volume 15, edition 2008 - Copper: It hardens the alloy, increasing yield strength and strength but decreasing elongation. The range of the old alloy 224 was 4.5 to 5.5%. experience acquired by the applicant with the B206 indicates that it is good to limit the copper to a maximum of 4.9% because beyond it is very difficult to put all the copper in solution. As the present results, obtained with a copper of 4.7 to 4.8%, show that the resistance to ambient temperature obtained with the addition of magnesium is very high but that the elongation is reduced compared to the old alloy 224 without magnesium, it is It is logical to foresee the possibility of reducing copper below 4.5%, and more particularly up to 3.5%. The Applicant has carried out work on alloy B206 for which it considers that the results which are transferable to the alloy according to the invention and show that a lowering of copper from 5.0% to 4.0% allows to gain significantly in elongation at the cost of a loss of resistance, but that it remains higher than 400 MPa. In view of some cylinder heads, it is even conceivable to accept a slightly larger drop in resistance to favor elongation and reduce copper up to 3.5%. We can choose subdomains between 3.5% and 4.9% depending on the trade-off of characteristics targeted for the specific part. In general, subdomains centered on 4.3% or 4.4% such as 3.8 - 4.9% and better 4.0 - 4.8% lead to a fairly balanced compromise.
- Manganese: this element must not exceed 0.70% otherwise the risk of forming coarse intermetallic phases. Since it generally improves the mechanical properties, especially when hot, a range of 0.20 to 0.50% similar to that of 206 type alloys is preferred.
- Zinc: this element is an impurity which, at high content, can decrease the mechanical properties and make the liquid bath more oxidizable. It may be envisaged to tolerate up to 0.30% in order to facilitate the use of recycle metal, but less than 0.10% and better still less than 0.03% is preferred for high performance parts.
- Nickel: it generally contributes to the mechanical strength when hot but considerably reduces elongation. As the hot resistance is ensured in the invention by the addition of other elements, copper, magnesium, vanadium and zirconium, nickel is considered here as an impurity, which is limited to a maximum of 0.30% for the purpose of facilitate the use of recycling metal, and preferably at 0.10% and even better at 0.03% for high performance parts.
- Vanadium: This peritectic element in particular improves the resistance to creep when hot. Applicant has observed that in another alloy base containing silicon, the creep resistance was greatly improved between 0 and 0.05%, then improved more gradually from 0.05% to 0.17% and was above 0.17%. % stable at an excellent level. Limiting the maximum level of vanadium to 0.15% as in the old 224 does not therefore seem desirable. In the alloy according to the invention, a level of 0.05 to 0.30% is provided, which can be tightened to narrower subdomains of 0.08 - 0.25% and preferably 0.10 - 0.20%.
- Zirconium: this peritectic element also improves in particular the resistance to hot creep, and its effect is additive to that of vanadium. A content of 0.05 - 0.25% and preferably 0.08 - 0.20% is retained.
- Titanium: This peritectic element has two different effects: on the one hand, it is often used as a refining element of the grain, often in combination with an addition of parent alloy or salt adding titanium and boron. However, there are other refining practices consisting of adding only products introducing titanium and boron, or even only boron, and in the latter case the presence of titanium is not favorable. On the other hand, titanium contributes to good resistance to creep hot, although less strongly than vanadium and zirconium, as the applicant has observed. A maximum content of 0.35% has therefore been retained, but an addition of 0.05 to 0.25% and even more preferably of 0.10 to 0.20% is preferred.
Les autres éléments sont à considérer comme des impuretés. Dans le but de faciliter le recyclage, on peut tolérer pour certaines pièces un niveau total maximum de 0.50%, mais de préférence pour les pièces sollicitées on adoptera des maximas de 0.15% au total et 0.05% chacun.The other elements are to be considered as impurities. In order to facilitate the recycling, we can tolerate for some parts a maximum total level of 0.50%, but preferably for the parts solicited we will adopt maxima of 0.15% in total and 0.05% each.
On a élaboré dans un four électrique de 35 kg une série de trois compositions d'alliages décrites dans le tableau 4, tous éléments exprimés en % pondéral.
Ces alliages ont été affinés par addition d'AlTi5B (30 ppm de titane ainsi ajouté) et dégazés par un traitement de 10 minutes à l'aide d'un rotor en graphite tournant à 300 tours / minute avec un débit d'argon de 5 litres / minute, le tout sous couverture d'un flux de lavage MgCl2 60% - KCl 40%.These alloys were refined by addition of AlTi5B (30 ppm of titanium thus added) and degassed by a 10 minute treatment using a graphite rotor rotating at 300 rpm with an argon flow of 5. liters / minute, all under cover of a
On a ensuite coulé des éprouvettes en coquille de diamètre ¼" (6.5 mm)du type de la société Rio Tinto Alcan représentées à la
On a d'abord déterminé la température de brûlure des différentes compositions en procédant à des analyses enthalpiques différentielles (AED) sur des pastilles usinées dans les éprouvettes coulées. La vitesse de montée en température a été de 20°C/minute. Les courbes d'AED sont représentées à la
La température de brûlure se décale progressivement vers les températures plus basses quand la teneur en Mg augmente de 0% à 0.09% puis 0.13%.The burn temperature gradually shifts to lower temperatures when the Mg content increases from 0% to 0.09% and then to 0.13%.
On a ensuite traité thermiquement ces 3 alliages en leur appliquant une mise en solution comportant un palier préliminaire de 2 h à 495°C puis un palier principal de 12 h à 528°C, suivi d'une trempe à l'eau à 65°C et d'un revenu de 4h à 200°C. On obtient ainsi un alliage à l'état T7.These 3 alloys were then heat treated by applying them to a solution comprising a preliminary stage of 2 hours at 495 ° C. and then a main stage of 12 hours at 528 ° C., followed by a quenching with water at 65 ° C. C and an income of 4h at 200 ° C. An alloy in the T7 state is thus obtained.
Les ébauches destinées aux essais de fluage ont subi, préalablement à ce traitement thermique, une compaction isostatique à chaud sous 1000 bar à 485°C pendant 2h afin d'éliminer toute microporosité qui pourrait affecter sérieusement les essais compte tenu du faible diamètre de l'éprouvette.The blanks intended for the creep tests were subjected, prior to this heat treatment, to hot isostatic compaction at 1000 bar at 485 ° C. for 2 hours in order to eliminate any microporosity which could seriously affect the tests given the small diameter of the specimen.
Les caractéristiques mécaniques statiques ont été mesurées à température ambiante et à 250°C et 300°C. Dans ces deux derniers cas, les éprouvettes ont été préchauffées pendant 100 h à la température considérée avant d'être tractionnées.Static mechanical characteristics were measured at room temperature and at 250 ° C and 300 ° C. In the latter two cases, the specimens were preheated for 100 hours at the temperature before being tracted.
Les résultats figurent dans les tableaux 6, 7 et 8 :
On a réalisé des essais de fluage à 300°C dans les conditions suivantes :
- Les éprouvettes de diamètre 4 mm dans la zone utile, usinées dans les ébauches de diamètre 12.7 mm, ont d'abord été préchauffées 100 h à 300°C dans un four séparé, puis placées sur la machine de fluage et stabilisées à nouveau ½ h à 300°C avant de les mettre sous une charge constante de 30 MPa. La déformation en % est alors enregistrée continûment pendant une durée de 300 h à 300°C. Le critère principal utilisé pour l'interprétation des essais est la déformation obtenue après 300 h.
- The test pieces with a diameter of 4 mm in the working zone, machined in blanks with a diameter of 12.7 mm, were first preheated for 100 h at 300 ° C. in a separate oven, then placed on the creep machine and stabilized again for ½ hour. at 300 ° C before putting them under a constant load of 30 MPa. The% strain is then recorded continuously for 300 hours at 300 ° C. The main criterion used for the interpretation of the tests is the deformation obtained after 300 h.
Le tableau 9 résume les résultats :
Ces résultats sont reportés dans la
Une pièce peut alors être moulée à partir de l'alliage avantageux définit ci-dessus, cette pièce pouvant notamment être une culasse ou un insert d'une culasse ou d'une autre pièce nécessitant une haute résistance mécanique statique à la température ambiante et à chaud et une haute tenue au fluage à chaud, en particulier à 300°C.A part may then be molded from the advantageous alloy defined above, this part may in particular be a cylinder head or an insert of a cylinder head or of another part requiring a high static mechanical resistance at room temperature and at room temperature. hot and high resistance to creep when hot, in particular at 300 ° C.
La pièce est avantageusement traitée T7, même si un traitement T6 est également envisageable.The part is advantageously treated T7, even if a T6 treatment is also possible.
Aussi, récemment, un nouveau procédé de fonderie nommé « Moulage par Ablation » a été introduit en Amérique du Nord. Ce procédé a été décrit dans l'article
Le moulage par ablation convient particulièrement au moulage des alliages à criquabilité élevée. Initialement, il s'agit de moulage sable qui contrarie fort peu le retrait, et ensuite après ablation du moule la fin de la solidification s'effectue sans moule rigide du tout. En plus d'assurer une vitesse de solidification élevée, le procédé conduit aussi à des gradients de température élevés car l'aspersion est généralement progressive, commençant sur certaines zones choisies et avançant vers les points de fin de solidification où il est possible d'attacher les masselottes. Ceci favorise avantageusement aussi l'utilisation d'alliages à faible capacité d'alimentation de la retassure, tel que les alliages aluminium cuivre, dont l'alliage selon l'invention.Ablation molding is particularly suitable for molding high-tread alloys. Initially, it is sand casting that does not much upset the withdrawal, and then after removal of the mold the end of the solidification is carried out without rigid mold at all. In addition to providing a high solidification rate, the process also leads to high temperature gradients because the spray is generally progressive, starting on selected areas and advancing towards the end points of solidification where it is possible to attach. the weights. This advantageously also favors the use of alloys with low feed capacity of the shrink, such as copper aluminum alloys, including the alloy according to the invention.
Aussi, l'invention a également pour objet un procédé pour mouler une pièce à partir de l'alliage selon l'invention, notamment un insert ou une culasse, comprenant les étapes consistant à :
- fournir un moule formé à partir d'un agrégat et d'un liant hydrosoluble ;
- couler l'alliage dans le moule ;
- projeter de l'eau sur le moule de manière à désagréger le moule et à refroidir l'insert ou la culasse pour accélérer la solidification de l'alliage.
- providing a mold formed from an aggregate and a water-soluble binder;
- pour the alloy into the mold;
- projecting water on the mold so as to disintegrate the mold and cool the insert or the cylinder head to accelerate the solidification of the alloy.
La mise en oeuvre de ce procédé permet avantageusement la production en grande série de pièces moulées avec l'alliage selon l'invention ayant des propriétés mécaniques à chaud bien plus élevées que les alliages aluminium silicium.The implementation of this method advantageously allows the mass production of molded parts with the alloy according to the invention having much higher mechanical properties than aluminum silicon alloys.
Les perspectives d'emploi d'alliages aluminium cuivre à haute résistance à chaud ne sont cependant pas restreintes au procédé par ablation : il existe d'autres voies dont le moulage au sable classique, éventuellement combiné à des refroidisseurs métalliques, et le moulage en moule métallique coquille, éventuellement avec des modifications de tracé des pièces permettant d'accepter les moins bonnes propriétés de fonderie de cette famille d'alliages.However, the prospects for using high-strength copper aluminum alloys are not restricted to the ablation process: there are other ways, including conventional sand casting, possibly combined with metal chillers, and mold casting. metallic shell, possibly with modifications of the part layout to accept the less good foundry properties of this family of alloys.
Claims (17)
- Cast part with high static mechanical strength at ambient and hot temperatures and high creep strength at high temperature, especially at 300° C and above, cast in aluminum alloy with the following chemical composition, expressed as percentages by weight:Si: 0.02 - 0.50%Fe: 0.02 - 0.30%Cu: 3.5 - 4.9%Mn: < 0.70%Mg: 0.05 - 0.20%Zn: < 0.30%Ni: < 0.30%V: 0.05 - 0.30%Zr: 0.05 - 0.25%Ti: 0.01 - 0.35%other elements in total < 0.15%; and less than 0.05% each,the remainder being aluminum;
- Cast part according to claim 1, characterized in that the magnesium content of the alloy is between 0.07 and 0.20%.
- Cast part according to either of claims 1 or 2 characterized in that the magnesium content lies between 0.08 and 0.20% and preferably between 0.09 and 0.13%.
- Cast part according to one of claims 1 to 3 characterized in that the copper content lies between 3.8 and 4.9% and preferably between 4.0 and 4.8%.
- Cast part according to any of the previous claims characterized in that the vanadium content is between 0.08 - 0.25% and preferably between 0.10 - 0.20%.
- Cast part according to any of the previous claims characterized in that the zirconium content lies between 0.08 and 0.20%.
- Cast part according to any of the previous claims characterized in that the titanium content lies between 0.05 and 0.25% and preferably between 0.10 and 0.20%.
- Cast part according to any of the previous claims characterized in that the silicon content lies between 0.02 and 0.20% and preferably between 0.02 and 0.06%.
- Cast part according to any of the previous claims characterized in that the iron content lies between 0.02 and 0.20%, preferably between 0.02 and 0.12% and more preferably between 0.02 and 0.06%.
- Cast part according to any of the previous claims characterized in that the manganese content lies between 0.20 and 0.50%.
- Cast part according to any of the previous claims characterized in that the zinc content is less than 0.10% and preferably less than 0.03%.
- Cast part according to any of the previous claims characterized in that the nickel content is less than 0.10% and preferably less than 0.03%.
- Cast part according to any of the previous claims having undergone T7 or T6 type heat treatment.
- Insert comprising a cast part according to any of claims 1 to 13.
- Insert according to claim 14, characterized in that said insert is essentially made up of the cast part.
- Cylinder head comprising a cast part according to any of claims 1 to 13 or an insert according to any of claims 14 and 15.
- Method for casting an insert according to any of claims 14 to 15 or a cylinder head according to claim 16, comprising stages of:- providing a mold formed from an aggregate and a water-soluble binder;- casting the alloy in the mold;- spraying water on the mold so as to break up the mold and cool the insert or cylinder head.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PL10799072T PL2516687T3 (en) | 2009-12-22 | 2010-12-07 | Casting made from copper containing aluminium alloy with high mechanical strength and hot creep |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0906218A FR2954355B1 (en) | 2009-12-22 | 2009-12-22 | COPPER ALUMINUM ALLOY MOLDED MECHANICAL AND HOT FLUID MOLDED PART |
PCT/FR2010/000812 WO2011083209A1 (en) | 2009-12-22 | 2010-12-07 | Copper aluminum alloy molded part having high mechanical strength and hot creep resistance |
Publications (2)
Publication Number | Publication Date |
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EP2516687A1 EP2516687A1 (en) | 2012-10-31 |
EP2516687B1 true EP2516687B1 (en) | 2016-08-10 |
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Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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EP10799072.3A Active EP2516687B1 (en) | 2009-12-22 | 2010-12-07 | Casting made from copper containing aluminium alloy with high mechanical strength and hot creep |
Country Status (11)
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US (1) | US20120258010A1 (en) |
EP (1) | EP2516687B1 (en) |
JP (1) | JP5758402B2 (en) |
KR (1) | KR101757013B1 (en) |
BR (1) | BR112012016917A2 (en) |
CA (1) | CA2812236C (en) |
ES (1) | ES2601809T3 (en) |
FR (1) | FR2954355B1 (en) |
MX (1) | MX2012006988A (en) |
PL (1) | PL2516687T3 (en) |
WO (1) | WO2011083209A1 (en) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
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US10266933B2 (en) * | 2012-08-27 | 2019-04-23 | Spirit Aerosystems, Inc. | Aluminum-copper alloys with improved strength |
FR3007423B1 (en) * | 2013-06-21 | 2015-06-05 | Constellium France | EXTRADOS STRUCTURE ELEMENT IN ALUMINUM COPPER LITHIUM ALUMINUM |
US9643651B2 (en) | 2015-08-28 | 2017-05-09 | Honda Motor Co., Ltd. | Casting, hollow interconnecting member for connecting vehicular frame members, and vehicular frame assembly including hollow interconnecting member |
DE102016200535A1 (en) * | 2016-01-18 | 2017-07-20 | Bayerische Motoren Werke Aktiengesellschaft | Method for producing an aluminum casting alloy |
CN107419148A (en) * | 2017-05-05 | 2017-12-01 | 安徽彩晶光电有限公司 | Al-alloy for liquid crystal television bracket |
CN112281034A (en) * | 2020-10-16 | 2021-01-29 | 中国航发北京航空材料研究院 | Cast aluminum alloy and preparation method thereof |
US20220170138A1 (en) * | 2020-12-02 | 2022-06-02 | GM Global Technology Operations LLC | Aluminum alloy for casting and additive manufacturing of engine components for high temperature applications |
CN114058917A (en) * | 2021-10-29 | 2022-02-18 | 安徽省恒泰动力科技有限公司 | Aluminum alloy applied to automobile engine cylinder and preparation method thereof |
CN114293077B (en) * | 2021-12-29 | 2022-09-30 | 北京理工大学 | High-strength aluminum-copper alloy for aerospace structural member and preparation method thereof |
CN116005022B (en) * | 2023-02-08 | 2024-06-07 | 内蒙古蒙泰集团有限公司 | High-performance cast aluminum-silicon alloy and preparation method thereof |
Family Cites Families (14)
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US165A (en) * | 1837-04-17 | Mode of propelling boats ost castals or rivers | ||
GB516423A (en) * | 1937-04-30 | 1940-01-02 | Edgar Hutton Dix Jr | Improvements in or relating to the heat treatment of aluminium base alloys |
US3857165A (en) * | 1973-05-04 | 1974-12-31 | Aluminum Co Of America | Welding aluminum |
US4610733A (en) * | 1984-12-18 | 1986-09-09 | Aluminum Company Of America | High strength weldable aluminum base alloy product and method of making same |
JPH0759731B2 (en) * | 1986-12-10 | 1995-06-28 | 石川島播磨重工業株式会社 | Casting Al (Cu) -Mg high-strength aluminum alloy and method for producing the same |
FR2690927B1 (en) * | 1992-05-06 | 1995-06-16 | Pechiney Aluminium | ALUMINUM-BASED MOLDING ALLOYS HAVING GOOD RESISTANCE TO HOT CREAM. |
JPH06262719A (en) * | 1993-03-11 | 1994-09-20 | Nippon Steel Corp | Aluminum alloy ply metal with excellent moldability, corrosion resistance and baking hardening property |
JPH0754088A (en) * | 1993-08-13 | 1995-02-28 | Nippon Steel Corp | Aluminum alloy clad plate excellent in formability, wear resistance and baking hardenability |
JPH1017975A (en) * | 1996-06-27 | 1998-01-20 | Kyushu Mitsui Alum Kogyo Kk | Aluminum alloy for casting |
JPH11302764A (en) * | 1998-04-17 | 1999-11-02 | Kobe Steel Ltd | Aluminum alloy excellent in high temperature characteristic |
US6368427B1 (en) * | 1999-09-10 | 2002-04-09 | Geoffrey K. Sigworth | Method for grain refinement of high strength aluminum casting alloys |
CN1112455C (en) * | 2001-07-26 | 2003-06-25 | 华南理工大学 | Aluminium-base cast alloy material with high tenacity and less hot cacking tendency |
US20070102071A1 (en) * | 2005-11-09 | 2007-05-10 | Bac Of Virginia, Llc | High strength, high toughness, weldable, ballistic quality, castable aluminum alloy, heat treatment for same and articles produced from same |
US20080041499A1 (en) * | 2006-08-16 | 2008-02-21 | Alotech Ltd. Llc | Solidification microstructure of aggregate molded shaped castings |
-
2009
- 2009-12-22 FR FR0906218A patent/FR2954355B1/en not_active Expired - Fee Related
-
2010
- 2010-12-07 KR KR1020127019244A patent/KR101757013B1/en active IP Right Grant
- 2010-12-07 EP EP10799072.3A patent/EP2516687B1/en active Active
- 2010-12-07 WO PCT/FR2010/000812 patent/WO2011083209A1/en active Application Filing
- 2010-12-07 BR BR112012016917A patent/BR112012016917A2/en not_active Application Discontinuation
- 2010-12-07 US US13/516,799 patent/US20120258010A1/en not_active Abandoned
- 2010-12-07 CA CA2812236A patent/CA2812236C/en active Active
- 2010-12-07 ES ES10799072.3T patent/ES2601809T3/en active Active
- 2010-12-07 JP JP2012545367A patent/JP5758402B2/en not_active Expired - Fee Related
- 2010-12-07 PL PL10799072T patent/PL2516687T3/en unknown
- 2010-12-07 MX MX2012006988A patent/MX2012006988A/en active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
KR20120114316A (en) | 2012-10-16 |
CA2812236C (en) | 2018-03-27 |
FR2954355A1 (en) | 2011-06-24 |
JP5758402B2 (en) | 2015-08-05 |
FR2954355B1 (en) | 2012-02-24 |
ES2601809T3 (en) | 2017-02-16 |
MX2012006988A (en) | 2012-07-03 |
BR112012016917A2 (en) | 2016-04-12 |
JP2013515169A (en) | 2013-05-02 |
KR101757013B1 (en) | 2017-07-11 |
PL2516687T3 (en) | 2017-07-31 |
US20120258010A1 (en) | 2012-10-11 |
CA2812236A1 (en) | 2011-07-14 |
EP2516687A1 (en) | 2012-10-31 |
WO2011083209A1 (en) | 2011-07-14 |
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