EP0896637B1 - Aluminium-silicon-magnesium alloy for motor vehicle body - Google Patents
Aluminium-silicon-magnesium alloy for motor vehicle body Download PDFInfo
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- EP0896637B1 EP0896637B1 EP97921897A EP97921897A EP0896637B1 EP 0896637 B1 EP0896637 B1 EP 0896637B1 EP 97921897 A EP97921897 A EP 97921897A EP 97921897 A EP97921897 A EP 97921897A EP 0896637 B1 EP0896637 B1 EP 0896637B1
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- 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
- C22F1/043—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 silicon as the next major constituent
-
- 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
- C22C21/02—Alloys based on aluminium with silicon as the next major constituent
-
- 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 the field of aluminum alloys of the AlSiMg type, or alloys of the 6000 series according to the classification of the Aluminum Association, intended especially to the manufacture of automobile body parts, for which the final income of the alloy is done during the paint curing operation.
- AlSiMg alloy sheets have been used for many years for the manufacture of exterior elements of automobile bodywork because they have a good formability before hardening, absence of Lüders lines at deep drawing and high mechanical strength after heat treatment comprising dissolution, quenching, maturation and tempering hardening.
- This hardening income can advantageously be obtained during the paint curing operation applied to the body element, which saves a specific treatment. This is what we usually call by hardening effect during cooking, or in English "bake hardening".
- US patent 4589932 also from ALCOA, relates to an alloy, subsequently registered under the designation AA 6013, of composition: If: 0.4 - 1.2 Mg: 0.5 - 1.3 Cu: 0.6 - 1.1 Mn: 0.1 - 1.0 and recommends an income of 2 to 15 h at a temperature above 182 ° C.
- This alloy has better mechanical strength and better indentation resistance than 6009 or 6010, as well as a more stable response to hardening.
- US Patent 4,614,552 to ALCAN relates to the AA 6111 alloy of composition: If: 0.6 - 1.0 Mg: 0.62 - 0.82 Cu: 0.65 - 0.79 Mn: 0.1 - 0.5 Fe ⁇ 0.4
- This alloy has a mechanical resistance greater than 6009 and a formability greater than 6010, as well as a good response to the curing by baking of the painting, which the patent recommends to carry out for approximately 1 h between 177 and 204 ° C.
- FIG. 2 of the patent compares, for the alloys 6009, 6010 and 6111, the curves of the yield strength as a function of the curing temperature at different rates of deformation, and clearly shows that at 150 ° C, hardening has not yet started in any of the cases shown and it doesn't start to be significant only above 180 ° C.
- ALCOA patent US 4,840,852 relates to an alloy with a higher copper content, this which explains its designation AA 2008 in the category of Al-Cu alloys of the series 2000. Its composition is: Si: 0.5 - 0.85 Mg: 0.25 - 0.55 Cu: 0.75 - 1.10 Fe: 0.05 - 0.4.
- the preferred range for tempering is 177 - 218 ° C, and above specifically, the range 190 - 204 ° C. The only example indicates an income at 204 ° C.
- the applicant's international application WO 95/14113 relates to a range of alloys of composition: Si: 0.5-1.3 Mg: 0.25-0.8 Cu ⁇ 0.9 Mn: 0.1 - 0.8 Fe ⁇ 0.5, with fine manganese precipitates of Al type (Mn, Fe) If and recommends a pre-income between hardening and maturation. Examples show all an income of 30 min at 180 ° C.
- the aim of the present invention is to select, in Al-Si-Mg-Cu alloys, a narrow range of composition which allows both to achieve resistance sufficient mechanical after firing around 150 - 155 ° C and put the alloy in easy solution.
- the subject of the invention is an aluminum alloy capable of being used for the manufacture of exterior parts of automobile bodywork, of composition (% by weight): If: 0.5 -0 8 Mg: 0.45 - 0.65 Cu: 0.55 - 0.75 Mn and / or Cr: 0.1 - 0.3 aluminum remains with the inevitable impurities, with: 1, 6 ⁇ Si + Mg + Cu ⁇ 2
- Mg is between 0.50 and 0.60% and Cu between 0.60 and 0.70%.
- the range of composition of the alloys according to the invention is, for Si and Mg, at inside the range 6009/6010, but with a higher copper content. Through compared to the 6111 domain, it is less loaded with magnesium, whereas on the contrary it is more so than in 2008. But its main characteristic is to have, for compared to recent body alloys with high resistance and good formability, a total quantity of addition elements, represented by the sum Si + Mg + Cu, plus low. This feature allows homogenization and implementation solution under easier conditions, but, in the area of narrow composition of the invention, this reduction does not lead, as might have been expected, to a reduction in mechanical resistance on the finished part after dissolving short and an income practiced during a paint curing around 150 ° C.
- the alloy according to the invention is cast in the form of plates, homogenized between 500 and 580 ° C, hot rolled to a thickness between 10 and 3 mm, then rolled to cold to final thickness, generally included, for bodywork applications automotive, between 0.8 and 1.5 mm. Annealing from 1 h to 10 h between 300 and 500 ° C can be applied to the strip after hot rolling or during cold rolling.
- the strip is dissolved between 500 and 560 ° C for a period of between 20 s and 2 min. It is followed by quenching and maturing at room temperature for more than a week.
- the bodywork parts generally shaped by stamping and covered with paint, are subjected to an operation of baking the paint at a temperature below 170 ° C, most often around 150 ° C, and the income caused by this cooking, an elastic limit R 0.2 > 170 MPa can be reached on the part.
- compositions according to the invention thus lead to complete dissolution, favorable to the formability of the sheet, within a period compatible with the requirements industrial productivity.
- mechanical strength, after this short dissolution and an income associated with cooking the paintings towards 150 to 155 ° C is of the same order, and even sometimes better, than that of alloys of the prior art, however, more loaded with addition elements.
- the alloys A and B are in accordance with the invention, the sum Si + Mg + Cu being 1.71 and 1.91 respectively.
- Alloy F, type AA 6013 has an Mg content> 0.65.
- the plates were homogenized for 24 h at a temperature of 555 ° C for the alloy C and 570 ° C for the other 5.
- the efficiency of this homogenization can be assessed, in a manner known per se, by a differential enthalpy analysis (AED) on the homogenized plates. Indeed, if the homogenization is well done, this analysis leads to low peak areas (measured in J / g) and to high peak start temperatures.
- the results obtained were as follows (Table 2): Alloy Peak area (J / g) Temperature (° C) AT - 0.015 580 B - 0.088 568 VS - 1.52 563 D - 1.04 575 E - 0.075 563 F - 0.33 580
- the 2 alloys according to the invention have a lower peak area than the other 4, which indicates that their homogenization has been more complete.
- the plates then followed a simulated annealing of the hot rolling by maintaining for 9 h at 500 ° C and cooling at a speed of 25 ° C / h. Then cold rolling to the thickness of 1 mm was carried out, followed by dissolution in a salt bath, partly at 550 ° C, and partly at 525 ° C, for respective durations of 30, 60, 300 and 1800 s, and finally to a hardening.
- the quality of the solution can be assessed by differential enthalpy analysis of the samples in solution. The results of this analysis are as follows for a dissolution of 30 s at 550 ° C.
- the 2 alloys according to the invention have a peak area less than 4 others, which shows a better solution.
- the elastic limit of the alloy A is of the same order as that of D, and that of B is greater than that of C and D, then that alloys A and B are less loaded with additives than alloys C and D (lower Si + Mg + Cu sum).
- alloy A has the same level of elastic limit as the alloys C, D and F, while it is significantly less loaded with addition elements hardening, and that, surprisingly, alloy B has an elastic limit higher than that of alloys C to F.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Paints Or Removers (AREA)
- Conductive Materials (AREA)
- Cookers (AREA)
- Laminated Bodies (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
L'invention concerne le domaine des alliages d'aluminium du type AlSiMg, ou alliages de la série 6000 selon la classification de l'Aluminum Association, destinés notamment à la fabrication d'éléments de carrosserie automobile, pour lesquels le revenu final de l'alliage se fait au cours de l'opération de cuisson de la peinture.The invention relates to the field of aluminum alloys of the AlSiMg type, or alloys of the 6000 series according to the classification of the Aluminum Association, intended especially to the manufacture of automobile body parts, for which the final income of the alloy is done during the paint curing operation.
Les tôles en alliages du type AlSiMg sont utilisées depuis de nombreuses années pour la fabrication d'éléments extérieurs de carrosserie automobile car ils présentent une bonne formabilité avant durcissement, une absence de lignes de Lüders à l'emboutissage et une résistance mécanique élevée après un traitement thermique comportant une mise en solution, une trempe, une maturation et un revenu de durcissement. Ce revenu de durcissement peut se faire avantageusement au cours de l'opération de cuisson de la peinture appliquée sur l'élément de carrosserie, ce qui permet d'économiser un traitement spécifique. C'est ce qu'on désigne habituellement par effet de durcissement à la cuisson, ou en anglais « bake hardening ».AlSiMg alloy sheets have been used for many years for the manufacture of exterior elements of automobile bodywork because they have a good formability before hardening, absence of Lüders lines at deep drawing and high mechanical strength after heat treatment comprising dissolution, quenching, maturation and tempering hardening. This hardening income can advantageously be obtained during the paint curing operation applied to the body element, which saves a specific treatment. This is what we usually call by hardening effect during cooking, or in English "bake hardening".
De nombreux alliages ont été développés pour cette application. Le brevet-US 4082578 d'ALCOA décrit des alliages pour carrosserie automobile de composition (% en poids): Si: 0,4 - 1,2 Mg: 0,4 - 1,1 Cu: 0,1 - 0,6 Fe: 0,05 - 0,35 avec addition d'un ou plusieurs des éléments Mn, Cr ou Zr. Des alliages de ce type ont été enregistrés à l'Aluminum Association sous les désignations 6009 et 6010. Le revenu de durcissement de ces alliages est effectué de manière appropriée entre 190 et 205°C.Many alloys have been developed for this application. The US patent 4082578 of ALCOA describes alloys for automobile bodywork of composition (% by weight): Si: 0.4 - 1.2 Mg: 0.4 - 1.1 Cu: 0.1 - 0.6 Fe: 0.05 - 0.35 with the addition of one or more of the elements Mn, Cr or Zr. Alloys of this type have been registered with the Aluminum Association under the designations 6009 and 6010. The hardening income of these alloys is carried out appropriately between 190 and 205 ° C.
Le brevet US 4589932, également d'ALCOA, concerne un alliage, enregistré
ultérieurement sous la désignation AA 6013, de composition:
Si: 0,4 - 1,2 Mg: 0,5 - 1,3 Cu: 0,6 - 1,1 Mn: 0,1 - 1,0
et préconise un revenu de 2 à 15 h à une température supérieure à 182°C. Cet alliage
présente une meilleure résistance mécanique et une meilleure résistance à l'indentation
que le 6009 ou le 6010, ainsi qu'une réponse plus stable au durcissement.US patent 4589932, also from ALCOA, relates to an alloy, subsequently registered under the designation AA 6013, of composition:
If: 0.4 - 1.2 Mg: 0.5 - 1.3 Cu: 0.6 - 1.1 Mn: 0.1 - 1.0 and recommends an income of 2 to 15 h at a temperature above 182 ° C. This alloy has better mechanical strength and better indentation resistance than 6009 or 6010, as well as a more stable response to hardening.
Le brevet US 4614552 d'ALCAN est relatif à l'alliage AA 6111 de composition:
Si: 0,6 - 1,0 Mg: 0,62 - 0,82 Cu: 0,65 - 0,79 Mn: 0,1 - 0,5 Fe < 0,4US Patent 4,614,552 to ALCAN relates to the AA 6111 alloy of composition:
If: 0.6 - 1.0 Mg: 0.62 - 0.82 Cu: 0.65 - 0.79 Mn: 0.1 - 0.5 Fe <0.4
Cet alliage présente une résistance mécanique supérieure au 6009 et une formabilité supérieure au 6010, ainsi qu'une bonne réponse au durcissement par cuisson de la peinture, que le brevet préconise d'effectuer pendant environ 1 h entre 177 et 204°C. La figure 2 du brevet compare, pour les alliages 6009, 6010 et 6111, les courbes de la limite d'élasticité en fonction de la température de durcissement à différents taux de déformation, et montre clairement qu'à 150°C, le durcissement n'a pas encore commencé dans aucun des cas représentés et qu'il ne commence à être significatif qu'au-delà de 180°C.This alloy has a mechanical resistance greater than 6009 and a formability greater than 6010, as well as a good response to the curing by baking of the painting, which the patent recommends to carry out for approximately 1 h between 177 and 204 ° C. FIG. 2 of the patent compares, for the alloys 6009, 6010 and 6111, the curves of the yield strength as a function of the curing temperature at different rates of deformation, and clearly shows that at 150 ° C, hardening has not yet started in any of the cases shown and it doesn't start to be significant only above 180 ° C.
Le brevet US 4840852 d'ALCOA concerne un alliage à plus forte teneur en cuivre, ce qui explique sa désignation AA 2008 dans la catégorie des alliages Al-Cu de la série 2000. Il a pour composition: Si: 0,5 - 0,85 Mg: 0,25 - 0,55 Cu: 0,75 - 1,10 Fe: 0,05 - 0,4. La plage préférentielle pour le revenu est 177 - 218°C, et plus précisément, la plage 190 - 204°C. L'unique exemple indique un revenu à 204°C.ALCOA patent US 4,840,852 relates to an alloy with a higher copper content, this which explains its designation AA 2008 in the category of Al-Cu alloys of the series 2000. Its composition is: Si: 0.5 - 0.85 Mg: 0.25 - 0.55 Cu: 0.75 - 1.10 Fe: 0.05 - 0.4. The preferred range for tempering is 177 - 218 ° C, and above specifically, the range 190 - 204 ° C. The only example indicates an income at 204 ° C.
La demande internationale WO 95/14113 de la demanderesse est relative à une gamme d'alliages de composition: Si: 0,5- 1,3 Mg: 0,25 - 0,8 Cu < 0,9 Mn: 0,1 - 0,8 Fe < 0,5, avec de fins précipités au manganèse de type Al (Mn, Fe) Si et préconise un prérevenu entre la trempe et la maturation. Les exemples indiquent tous un revenu de 30 mn à 180°C.The applicant's international application WO 95/14113 relates to a range of alloys of composition: Si: 0.5-1.3 Mg: 0.25-0.8 Cu <0.9 Mn: 0.1 - 0.8 Fe <0.5, with fine manganese precipitates of Al type (Mn, Fe) If and recommends a pre-income between hardening and maturation. Examples show all an income of 30 min at 180 ° C.
Il existe depuis quelques années une tendance nette à la baisse de la température de cuisson des peintures dans l'industrie automobile, qui est passée de 180°C à environ 150°C. Cette baisse de température de cuisson a pour conséquence que le durcissement des alliages au cours de cette opération a tendance à s'amenuiser fortement. Il est donc devenu nécessaire, pour les panneaux extérieurs de carrosserie, de proposer des alliages qui soient suffisamment durs à des températures de cuisson faibles, tout en gardant une bonne formabilité après mise en solution, trempe et maturation à la température ambiante.There has been a clear downward trend in the temperature of baking of paints in the automotive industry, which went from 180 ° C to around 150 ° C. This drop in cooking temperature means that the hardening of alloys during this operation tends to decrease strongly. It therefore became necessary, for the exterior body panels, to offer alloys which are sufficiently hard at baking temperatures low, while maintaining good formability after dissolution, quenching and maturing at room temperature.
Par ailleurs, les impératifs de coût et de facilité de fabrication imposent de choisir des alliages faciles à mettre en solution, de manière à éviter des phases grossières non dissoutes néfastes à la formabilité.In addition, the imperatives of cost and ease of manufacture make it necessary to choose alloys easy to put in solution, so as to avoid coarse phases not dissolved harmful to formability.
Le but de la présente invention est de sélectionner, dans les alliages Al-Si-Mg-Cu, un domaine étroit de composition qui permette à la fois d'atteindre une résistance mécanique suffisante après une cuisson vers 150 - 155°C et de mettre l'alliage en solution de manière aisée.The aim of the present invention is to select, in Al-Si-Mg-Cu alloys, a narrow range of composition which allows both to achieve resistance sufficient mechanical after firing around 150 - 155 ° C and put the alloy in easy solution.
L'invention a pour objet un alliage d'aluminium apte à être utilisé pour la fabrication
de pièces extérieures de carrosserie automobile, de composition (% en poids):
Si: 0,5 -0 8 Mg: 0,45 - 0,65 Cu: 0,55 - 0,75 Mn et/ou Cr: 0,1 - 0,3
reste aluminium avec les impuretés inévitables, avec: 1,6 < Si + Mg + Cu < 2
De préférence, Mg est compris entre 0,50 et 0,60% et Cu entre 0,60 et 0,70%.The subject of the invention is an aluminum alloy capable of being used for the manufacture of exterior parts of automobile bodywork, of composition (% by weight):
If: 0.5 -0 8 Mg: 0.45 - 0.65 Cu: 0.55 - 0.75 Mn and / or Cr: 0.1 - 0.3 aluminum remains with the inevitable impurities, with: 1, 6 <Si + Mg + Cu <2
Preferably, Mg is between 0.50 and 0.60% and Cu between 0.60 and 0.70%.
Le domaine de composition des alliages selon l'invention se situe, pour Si et Mg, à l'intérieur du domaine 6009/6010, mais avec une teneur en cuivre plus élevée. Par rapport au domaine du 6111, il est moins chargé en magnésium, alors qu'au contraire il l'est plus par rapport au 2008. Mais sa principale caractéristique est d'avoir, par rapport aux alliages de carrosserie récents à haute résistance et bonne formabilité, une quantité totale d'éléments d'addition, représentée par la somme Si + Mg + Cu, plus faible. Cette particularité permet de procéder à l'homogénéisation et à la mise en solution dans des conditions plus aisées, mais, dans le domaine de composition étroit de l'invention, cette réduction n'entraíne pas, comme on aurait pu s'y attendre, une diminution de la résistance mécanique sur la pièce finie après une mise en solution courte et un revenu pratiqué lors d'une cuisson de peinture vers 150°C.The range of composition of the alloys according to the invention is, for Si and Mg, at inside the range 6009/6010, but with a higher copper content. Through compared to the 6111 domain, it is less loaded with magnesium, whereas on the contrary it is more so than in 2008. But its main characteristic is to have, for compared to recent body alloys with high resistance and good formability, a total quantity of addition elements, represented by the sum Si + Mg + Cu, plus low. This feature allows homogenization and implementation solution under easier conditions, but, in the area of narrow composition of the invention, this reduction does not lead, as might have been expected, to a reduction in mechanical resistance on the finished part after dissolving short and an income practiced during a paint curing around 150 ° C.
L'alliage selon l'invention est coulé sous forme de plaques, homogénéisé entre 500 et 580°C, laminé à chaud jusqu'à une épaisseur comprise entre 10 et 3 mm, puis laminé à froid à l'épaisseur finale, généralement comprise, pour les applications de carrosserie automobile, entre 0,8 et 1,5 mm. Un recuit de 1 h à 10 h entre 300 et 500°C peut être appliqué à la bande après laminage à chaud ou au cours du laminage à froid.The alloy according to the invention is cast in the form of plates, homogenized between 500 and 580 ° C, hot rolled to a thickness between 10 and 3 mm, then rolled to cold to final thickness, generally included, for bodywork applications automotive, between 0.8 and 1.5 mm. Annealing from 1 h to 10 h between 300 and 500 ° C can be applied to the strip after hot rolling or during cold rolling.
La mise en solution de la bande se fait entre 500 et 560°C pendant une durée comprise entre 20 s et 2 mn. Elle est suivie d'une trempe et d'une maturation à la température ambiante d'une durée supérieure à une semaine. Les pièces de carrosserie, généralement mises en forme par emboutissage et recouvertes de peinture, sont soumises à une opération de cuisson de la peinture à une température inférieure à 170°C, se situant le plus souvent autour de 150°C, et le revenu provoqué par cette cuisson permet d'atteindre sur la pièce une limite élastique R0,2 > 170 MPa.The strip is dissolved between 500 and 560 ° C for a period of between 20 s and 2 min. It is followed by quenching and maturing at room temperature for more than a week. The bodywork parts, generally shaped by stamping and covered with paint, are subjected to an operation of baking the paint at a temperature below 170 ° C, most often around 150 ° C, and the income caused by this cooking, an elastic limit R 0.2 > 170 MPa can be reached on the part.
Les compositions selon l'invention conduisent ainsi à une mise en solution complète, favorable à la formabilité de la tôle, dans une durée compatible avec les exigences industrielles de productivité. De manière inattendue, la résistance mécanique, après cette mise en solution courte et un revenu associé à une cuisson des peintures vers 150 à 155°C, est du même ordre, et même parfois meilleure, que celle d'alliages de l'art antérieur pourtant plus chargés en éléments d'addition.The compositions according to the invention thus lead to complete dissolution, favorable to the formability of the sheet, within a period compatible with the requirements industrial productivity. Unexpectedly, the mechanical strength, after this short dissolution and an income associated with cooking the paintings towards 150 to 155 ° C, is of the same order, and even sometimes better, than that of alloys of the prior art, however, more loaded with addition elements.
On a coulé des plaques en format 30 x 180 x 250 mm de 6 alliages dont la
composition est indiquée au tableau 1 (en % en poids).
Les alliages A et B sont conformes à l'invention, la somme Si + Mg + Cu étant respectivement 1,71 et 1,91. The alloys A and B are in accordance with the invention, the sum Si + Mg + Cu being 1.71 and 1.91 respectively.
L'alliage C, du type AA 6056, est plus chargé,avec Si > 0,8, la somme Si + Mg + Cu = 2,27, et les teneurs en Mn et Cr en dessous de celles des alliages de l'invention. L'alliage D est un AA 6111 classique avec Mg > 0,65 et Si + Mg + Cu = 2,02. L'alliage E a un Si > 0,8 et une somme Si + Mg + Cu = 2,19. L'alliage F, du type AA 6013, a une teneur en Mg > 0,65.Alloy C, type AA 6056, is more charged, with Si> 0.8, the sum Si + Mg + Cu = 2.27, and the contents of Mn and Cr below those of the alloys of the invention. Alloy D is a classic AA 6111 with Mg> 0.65 and Si + Mg + Cu = 2.02. The alloy E has a Si> 0.8 and a sum Si + Mg + Cu = 2.19. Alloy F, type AA 6013, has an Mg content> 0.65.
Les plaques ont été homogénéisées pendant 24 h à une température de 555°C pour
l'alliage C et 570°C pour les 5 autres. L'efficacité de cette homogénéisation peut être
appréciée, de manière connue en soi, par une analyse enthalpique différentielle (AED)
sur les plaques homogénéisées. En effet, si l'homogénéisation est bien faite, cette
analyse conduit à des aires de pic (mesurées en J/g) faibles et à des températures de
début de pic élevées. Les résultats obtenus ont été les suivants (tableau 2):
On constate que les 2 alliages selon l'invention présentent une aire de pic plus faible que les 4 autres, ce qui indique que leur homogénéisation a été plus complète.It is noted that the 2 alloys according to the invention have a lower peak area than the other 4, which indicates that their homogenization has been more complete.
Les plaques ont suivi ensuite un recuit de simulation du laminage à chaud par maintien
de 9 h à 500°C et refroidissement à une vitesse de 25°C/h. On a procédé ensuite à un
laminage à froid jusqu'à l'épaisseur de 1 mm, puis à une mise en solution en bain de
sel, pour partie à 550°C, et pour partie à 525°C, pendant des durées respectives de
30, 60, 300 et 1800 s, et enfin à une trempe. Comme pour l'homogénéisation, on peut
apprécier la qualité de la mise en solution par analyse enthalpique différentielle des
échantillons mis en solution. Les résultats de cette analyse sont les suivants pour une
mise en solution de 30 s à 550°C (tableau 3):
On constate que les 2 alliages selon l'invention ont une aire de pic inférieure aux 4 autres, ce qui montre une meilleure mise en solution.It can be seen that the 2 alloys according to the invention have a peak area less than 4 others, which shows a better solution.
Les échantillons mis en solution ont subi ensuite une maturation à température ambiante pendant 3 semaines, une traction à 2% de déformation et un revenu en bain d'huile de 20 mn à 155°C.The samples in solution were then matured at temperature ambient for 3 weeks, traction at 2% deformation and an income in the bath oil for 20 min at 155 ° C.
Les limites élastiques R0,2 (en MPa) à l'état T4 obtenues pour les 4 alliages A, B, C et
D en fonction de la température et de la durée de mise en solution, sont indiquées au
tableau 4:
On peut tirer de ces résultats les conclusions suivantes: pour les alliages A et B selon l'invention, l'augmentation de la durée de mise en solution ne conduit pas à une augmentation significative de la résistance mécanique. On atteint le maximum de limite élastique pour un traitement de 30 s à 525°C pour l'alliage A, et pour un traitement de 30 s à 550°C pour l'alliage B. Au contraire, la mise en solution n'est pas complète après 1800 s à 550°C pour les alliages C et D. Cette mise en solution incomplète est néfaste pour la formabilité.The following conclusions can be drawn from these results: for alloys A and B according to the invention, the increase in the dissolution time does not lead to a significant increase in mechanical strength. We reach the maximum of elastic limit for a treatment of 30 s at 525 ° C for alloy A, and for a treatment of 30 s at 550 ° C for alloy B. On the contrary, the dissolution is not complete after 1800 s at 550 ° C for alloys C and D. This dissolution incomplete is detrimental to formability.
Par ailleurs, après une mise en solution courte (30 s), la limite élastique de l'alliage A est du même ordre que celle de D, et celle de B est supérieure à celle de C et D, alors que les alliages A et B sont moins chargés en éléments d'addition que les alliages C et D (somme Si + Mg + Cu inférieure).Furthermore, after a short solution time (30 s), the elastic limit of the alloy A is of the same order as that of D, and that of B is greater than that of C and D, then that alloys A and B are less loaded with additives than alloys C and D (lower Si + Mg + Cu sum).
Les limites d'élasticité obtenues après mise en solution de 1 mn à 550°C, trempe,
déformation de 2% et cuisson de 20 mn à 155°C sont données au tableau 5:
On constate que l'alliage A présente le même niveau de limite d'élasticité que les alliages C, D et F, alors qu'il est nettement moins chargé en éléments d'addition durcissants, et que, de manière surprenante, l'alliage B a une limite d'élasticité supérieure à celle des alliages C à F.It is found that alloy A has the same level of elastic limit as the alloys C, D and F, while it is significantly less loaded with addition elements hardening, and that, surprisingly, alloy B has an elastic limit higher than that of alloys C to F.
Claims (5)
- Aluminum alloy particularly intended for the manufacture of external automobile bodywork components, of composition (% by weight)
Si: 0.5 - 0.8 Mg: 0.45 - 0.65 Cu: 0.55 - 0.75
Mn and/or Cr: 0.1 - 0.3, the remainder being aluminum with the inevitable impurities
and with 1.6 < Si + Mg + Cu < 2.0. - Aluminum alloy according to Claim 1, characterized in that Mg is between 0.50 and 0.60%.
- Aluminum alloy according to one of Claims 1 and 2, characterized in that Cu is between 0.60 and 0.70%.
- Method of manufacturing a painted bodywork component made of an alloy according to one of Claims 1 to 3, comprising:casting a plate of alloy with the composition given,homogenization of this plate at a temperature between 500 and 580°Chot rolling of the plate into strip with a thickness of between 10 mm and 3 mm, followed by cold rolling to a thickness of between 0.8 and 1.5 mm,solution heat treatment of the rolled strip at a temperature between 500 and 560°C for a period of between 20 seconds and 2 minutes, followed by quenching and natural aging for more than one week at ambient temperature,manufacture of a component from this strip and coating it with liquid paint,curing of this paint at a temperature of between 150 and 170°C.
- Method according to Claim 4 in which, after hot rolling or during the cold rolling, the strip is subjected to annealing for a period of from 1 hour to 10 hours at between 300 and 500°C.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9605595A FR2748035B1 (en) | 1996-04-29 | 1996-04-29 | ALUMINUM-SILICON-MAGNESIUM ALLOY FOR AUTOMOTIVE BODYWORK |
FR9605595 | 1996-04-29 | ||
PCT/FR1997/000755 WO1997041272A1 (en) | 1996-04-29 | 1997-04-28 | Aluminium-silicon-magnesium alloy for motor vehicle body |
Publications (3)
Publication Number | Publication Date |
---|---|
EP0896637A1 EP0896637A1 (en) | 1999-02-17 |
EP0896637B1 true EP0896637B1 (en) | 2000-05-24 |
EP0896637B2 EP0896637B2 (en) | 2005-07-27 |
Family
ID=9491836
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP97921897A Expired - Lifetime EP0896637B2 (en) | 1996-04-29 | 1997-04-28 | Use of aluminium-silicon-magnesium alloy for manufacturing of motor vehicle body parts and method for manufacturing the same. |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0896637B2 (en) |
DE (1) | DE69702133T3 (en) |
ES (1) | ES2146467T5 (en) |
FR (1) | FR2748035B1 (en) |
WO (1) | WO1997041272A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2855083B1 (en) | 2003-05-20 | 2006-05-26 | Pechiney Rhenalu | PROCESS FOR MANUFACTURING FRICTION-WELDED ALUMINUM ALLOY PARTS |
FR2856368B1 (en) * | 2003-06-18 | 2005-07-22 | Pechiney Rhenalu | BODY PIECE OF AUTOMOBILE BODY IN ALLOY SHEET AI-SI-MG FIXED ON STRUCTURE STEEL |
DE102004035043A1 (en) * | 2004-07-20 | 2006-04-13 | Daimlerchrysler Ag | Shaping of light metal sheet by a shaping tool useful for shaping metal sheets in vehicle production specific heat with treatment prior to shaping at temperatrure below light metal melting point |
EP2096187A1 (en) | 2008-02-28 | 2009-09-02 | Georg Fischer Engineering AG | Method for simultaneous tempering and coating an aluminium component and component manufactured according to this method |
ES2929001T3 (en) * | 2019-12-23 | 2022-11-24 | Novelis Koblenz Gmbh | Manufacturing process of an aluminum alloy rolled product |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4784921A (en) * | 1985-11-04 | 1988-11-15 | Aluminum Company Of America | Aluminum alloy automotive material |
JPH04247842A (en) * | 1991-01-25 | 1992-09-03 | Sky Alum Co Ltd | Aluminum alloy sheet for automobile wheel and its manufacture |
JPH06289852A (en) * | 1993-04-02 | 1994-10-18 | Yamaha Corp | Pedal keyboard structure |
Family Cites Families (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2601040B1 (en) * | 1986-07-07 | 1988-09-02 | Cegedur | SOLDERABLE AND WELDABLE ALUMINUM ALLOY AND MANUFACTURING METHOD THEREOF |
FR2642436B1 (en) * | 1988-12-21 | 1991-06-14 | Pechiney Rhenalu | A1 ALLOY CONTAINING ESSENTIALLY SI, MG AND CU FOR STAMPING |
JPH05125506A (en) * | 1991-10-31 | 1993-05-21 | Furukawa Alum Co Ltd | Manufacture of baking hardenability aluminum alloy plate for forming |
JPH05306440A (en) * | 1992-04-30 | 1993-11-19 | Furukawa Alum Co Ltd | Manufacture of aluminum alloy sheet for forming excellent baking hardenability |
JPH0747808B2 (en) * | 1993-02-18 | 1995-05-24 | スカイアルミニウム株式会社 | Method for producing aluminum alloy sheet excellent in formability and bake hardenability |
US5616189A (en) * | 1993-07-28 | 1997-04-01 | Alcan International Limited | Aluminum alloys and process for making aluminum alloy sheet |
FR2713664B1 (en) * | 1993-11-17 | 1996-05-24 | Pechiney Rhenalu | Al-Si-Mg alloy with improved ductility and stampability and process for obtaining it. |
JPH07197219A (en) * | 1993-12-28 | 1995-08-01 | Furukawa Electric Co Ltd:The | Production of aluminum alloy sheet for forming |
JPH0860285A (en) * | 1994-06-16 | 1996-03-05 | Furukawa Electric Co Ltd:The | Bumper reinforcement made of aluminum alloy and its production |
US5662750A (en) * | 1995-05-30 | 1997-09-02 | Kaiser Aluminum & Chemical Corporation | Method of manufacturing aluminum articles having improved bake hardenability |
-
1996
- 1996-04-29 FR FR9605595A patent/FR2748035B1/en not_active Expired - Fee Related
-
1997
- 1997-04-28 WO PCT/FR1997/000755 patent/WO1997041272A1/en active IP Right Grant
- 1997-04-28 EP EP97921897A patent/EP0896637B2/en not_active Expired - Lifetime
- 1997-04-28 DE DE69702133T patent/DE69702133T3/en not_active Expired - Lifetime
- 1997-04-28 ES ES97921897T patent/ES2146467T5/en not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4784921A (en) * | 1985-11-04 | 1988-11-15 | Aluminum Company Of America | Aluminum alloy automotive material |
JPH04247842A (en) * | 1991-01-25 | 1992-09-03 | Sky Alum Co Ltd | Aluminum alloy sheet for automobile wheel and its manufacture |
JPH06289852A (en) * | 1993-04-02 | 1994-10-18 | Yamaha Corp | Pedal keyboard structure |
Non-Patent Citations (1)
Title |
---|
GUPTA ET AL: 'THE PROPERTIES AND CHARACTERISTICS OF TWO NEW AUTOMOTIVE ALUMINIUM CLOSURE PANEL MATERIALS', SAE, CONGRES DU 26-29 FEVRIER 1996, DETROIT, MICHIGAN, USA. * |
Also Published As
Publication number | Publication date |
---|---|
DE69702133T3 (en) | 2006-04-20 |
EP0896637B2 (en) | 2005-07-27 |
FR2748035A1 (en) | 1997-10-31 |
WO1997041272A1 (en) | 1997-11-06 |
DE69702133T2 (en) | 2000-11-09 |
ES2146467T5 (en) | 2006-03-01 |
FR2748035B1 (en) | 1998-07-03 |
ES2146467T3 (en) | 2000-08-01 |
EP0896637A1 (en) | 1999-02-17 |
DE69702133D1 (en) | 2000-06-29 |
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