EP2471967A1 - Method for obtaining improved mechanical properties in recycled aluminium castings free of platelet-shaped beta-phases - Google Patents

Method for obtaining improved mechanical properties in recycled aluminium castings free of platelet-shaped beta-phases Download PDF

Info

Publication number
EP2471967A1
EP2471967A1 EP10382360A EP10382360A EP2471967A1 EP 2471967 A1 EP2471967 A1 EP 2471967A1 EP 10382360 A EP10382360 A EP 10382360A EP 10382360 A EP10382360 A EP 10382360A EP 2471967 A1 EP2471967 A1 EP 2471967A1
Authority
EP
European Patent Office
Prior art keywords
aluminium alloy
casting
iron
aluminium
presenting
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP10382360A
Other languages
German (de)
French (fr)
Other versions
EP2471967B1 (en
Inventor
Ana Isabel Fernández Calvo
Andrea Niklas
Ignacio Alfaro Abreu
Iñigo Anza Ortiz de Apodaca
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Befesa Aluminio SL
Casa Maristas Azterlan
Original Assignee
ALUMINIO SL
Aluminio S L
Casa Maristas Azterlan
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=44279841&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=EP2471967(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by ALUMINIO SL, Aluminio S L, Casa Maristas Azterlan filed Critical ALUMINIO SL
Priority to EP20100382360 priority Critical patent/EP2471967B1/en
Priority to ES10382360.5T priority patent/ES2507865T3/en
Priority to PCT/ES2011/070911 priority patent/WO2012089886A2/en
Publication of EP2471967A1 publication Critical patent/EP2471967A1/en
Application granted granted Critical
Publication of EP2471967B1 publication Critical patent/EP2471967B1/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • 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
    • C22C21/04—Modified aluminium-silicon alloys
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C1/00—Making non-ferrous alloys
    • C22C1/02—Making non-ferrous alloys by melting
    • C22C1/026—Alloys based on aluminium
    • C—CHEMISTRY; METALLURGY
    • C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22C—ALLOYS
    • C22C1/00—Making non-ferrous alloys
    • C22C1/02—Making non-ferrous alloys by melting
    • C22C1/03—Making non-ferrous alloys by melting using master alloys
    • 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

Definitions

  • the present invention relates to aluminium alloys, more particularly, it relates to aluminium alloy castings suitable as components for instance for vehicles, machines and electric applications which are required to have high strength and high elongation values among other properties.
  • the present invention also relates to a process for its preparation from recycled aluminium alloys in order to obtain recycled aluminium casting free of platelet-shaped beta-phases.
  • Aluminium alloys are widely used in diverse applications for instance as components in the automotive, aerospace, industrial machines, electric applications etc., because of their excellent mechanical properties as well as other technological properties such as corrosion resistance and reduced hot cracking tendency.
  • the primary production which is of minerals rich in aluminium (bauxite)
  • aluminium recycling secondary alloy whose raw material is dross and other residues rich in aluminium.
  • the primary alloy production consists basically in reducing the oxide present in bauxite enhancing the purity of aluminium by electrolysis.
  • the most important drawback of this method is the high quantity of energy (from 14 to 15 Kwh/kg) which is necessary to produce aluminium whereas in the aluminium recycling method the costs are about 0,5-0,75 Kwh/kg, that is lower than 5% of the primary production.
  • AlSiMg alloys are nowadays one of the most common aluminium castings alloys for high safety parts, such as automotive or aerospace components, which require high mechanical properties. This alloy presents also high ductility due to the low content in impurities and to the addition of elements such as Ti or Sr which refine and modify the microstructure, respectively. AlSiMg alloys are broadly used for castings produced in sand, permanent and investment moulds.
  • the high content in impurities, especially the high iron content, in secondary alloys (recycled aluminium) is considered as the main disadvantage.
  • the iron content increases in recycled aluminium after each subsequent melting; its elimination or reduction is technically very complex and rather expensive, not being economically feasible.
  • the microstructure of AlSiMg alloys presents alpha aluminium dendrites and Al-Si eutectic and other intermetallic phases among which the iron-rich ones can be highlighted.
  • Iron is well known for being the most common and detrimental impurity in aluminium alloys for mechanical properties, promoting the appearance of hard and brittle intermetallic iron-rich phases during solidification.
  • the platelet-shaped beta phase (Al 5 FeSi) is the most prejudicial since it is well known that ductility and toughness are significantly decreased. Therefore, there has been recently an increasing interest in developing methods for producing improved recycled aluminium alloys in which the formation of the beta phase is reduced and the mechanical properties are thus improved.
  • the strategy was based on the inhibition of the platelet morphology by promoting the precipitation of the Al 15 Fe 3 Si 2 -type phase with the addition of a neutralizing element (Mn, Cr, Co and Be) and in some case controlling the condition of crystallization.
  • a neutralizing element Mn, Cr, Co and Be
  • the patent WO 97/13882 discloses a method for producing iron-containing AlSi-alloys in particular Al-Si-Mn-Fe- alloys.
  • the mechanical properties of aforementioned Al-alloys with iron contents between 0,4 and 2.0 wt.% can be improved by controlling the morphology of the iron containing intermetallic precipitates.
  • the precipitation of platelet-shaped beta phase ( ⁇ -Al 5 FeSi) has been found to be suppressed by a primary precipitation of the hexagonal Al 8 Fe 2 Si-type phase which is in turn less harmful one.
  • the method comprises further controlling the condition of the crystallization by the addition of one or more elements such as Ti, Zr, Sr, Na and Ba.
  • One aspect of the present invention refers to an iron containing aluminium alloy, hereinafter referred to as the alloy of the invention, which is free from primary platelet-shaped beta-phase of the Al 5 FeSi-type in the solidified structure presenting the following compositions (amounts expressed in weight percentage, wt.% in respect to the total weight of the alloy): Si 6.00 - 9.50 Fe 0.15 - 0.60 Mn 0.04 - 0.60 Mg 0.20 - 0.70 Cr 0.01 - 0.60 Ti 0.05 - 0.30 Sr and/or Na 0.001 - 0.25 V 0.00 - 0.60 Cu 0.01 - 0.25 Ni 0.01 - 0.1 Zn 0.01 - 0.1
  • the iron-containing aluminium alloy of the invention presents a composition characterized in that the amount of Mn plus Cr in weight percentage is equal or larger than 50 % of Fe amount.
  • the iron-containing aluminium alloy of the invention presents a composition characterized in that the amount of Mn plus Cr plus V in weight percentage is equal or larger than 50 % of Fe amount.
  • the iron-containing aluminium alloy of the invention presents a Fe content between 0.15 - 0.40% in weight percentage and an amount of Mn plus Cr plus V comprised between 0.15 - 0.40 wt.%.
  • the present invention refers to a process for the preparation of the aluminium alloy of the invention comprising the following steps:
  • the process of the invention comprises the degassing process according to already known methods such as treating the molten alloy with dry nitrogen or dry argon until the hydrogen content dissolved in the melt is low enough.
  • the process comprises the addition of alloying elements added as pure elements or as master alloys.
  • the present invention resides in the addition of alloying elements: Mn+Cr o Mn+Cr+V, to the base composition of a secondary AlSi7Mg ingot of second fusion (or recycled aluminium).
  • the process comprises the addition of grain refiner and eutectic modification agents by means of master alloys additions.
  • the modifier agent Na or Sr are the most common ones and are added to achieve the modification of the eutectic Al-Si structure, which precipitates during solidification, showing a rounded morphology instead of needle structure, typical when such a modifying agent is not added. It is well known that the presence of such needle structures reduces the mechanical properties (ductility, strength) of the alloys, promoting the appearance of cracks.
  • TiB master alloys are used to obtain a microstructures which shows a fine grain size and thus improving the final mechanical properties and also, reducing the porosity tendency.
  • the platelet-shaped beta phases (Al 5 FeSi), so detrimental for the final mechanical properties, disappear and are substituted by globular-shaped alpha-phases (Al 8 Fe 2 Si) obtaining a substantial improvement in mechanical properties (Tensile strength, yield stress and elongation).
  • the properties of the recycled alloys obtained according to the process of the present invention show mechanical properties comparable to those obtained in primary alloys.
  • step e the degassed molten alloy is poured into a sand and permanent mould. After filling the mould the cast alloy solidifies and an aluminium casting is obtained.
  • a T6 treatment comprises a first step of solution heat treatment, heating the castings at a temperature between 500 to 600oC for 2 to 6 hours, followed by quenching.
  • the second step will consist in an artificial aging at a temperature between 150 to 180oC for 2 to 8 hours.
  • an aluminium alloy casting obtainable by the above defined process presenting a tensile strength between 250-300 MPa, a yield strength between 190-230 MPa and elongation values between 4,5-9%.
  • the aluminium alloy casting of the invention can be used as a component for transport components such as wheels, suspension parts, brake parts, and energetic industry components.
  • a further aspect of the invention relates to a component made from recycled aluminium alloy castings such as steering knuckle, master cylinder and brake calliper.
  • tensile test specimen are poured in sand mould and permanent moulds from the aluminium alloy of the invention with additions of Mn, Cr and V.
  • the mechanical properties were determined with tensile test specimen according to norm (UNE UNE-EN_1706), (see fig 2 ).
  • the aluminium alloys present a tensile strength of at least 250 MPa, a yield strength of at least 190 MPa and an elongation of at least 4.5 %.
  • the test pieces according to the invention were submitted to microstructural analysis. The inventors found that the addition of controlled amounts of Mn, Cr and V according to the present invention eliminates the platelet-shape beta-phases (Al 5 FeSi).
  • the aluminium alloys have been produced by using secondary AlSi7Mg ingots, obtained from scrap, recycled aluminium dross and other metal residues rich in aluminium.
  • the following table shows the chemical compositions of recycled ingots used in the examples, with iron contents between 0.28 and 0.34 wt.%.
  • Three recycled ingots (ref. I, II and III) have been used in the experimental tests (Base Composition) are shown, the rest being Al: Ingot Secondary AlSi7Mg alloy Chemical Composition (wt.%) Si Fe Cu Mn Mg Cr Ni Zn Ti Sr V Ref. I 7.11 0.34 0.06 0.09 0.27 0.017 0.01 0.07 0.07 0.005 ⁇ 0.01 Ref. II 6.94 0.28 0.04 0.04 0.28 0.004 0.00 0.04 0.14 ⁇ 0.003 ⁇ 0.01 Ref. III 6.92 0.28 0.04 0.04 0.25 ⁇ 0.01 0.01 0.04 0.16 ⁇ 0.003 ⁇ 0.01 Aluminium in balance
  • the recycled ingots were melted in an electric furnace (capacity of 50 kg of molten aluminium) at 710-750oC. The melt was then alloyed and liquid treated according to the predetermined following schedule:
  • the melt was held for 10 minutes between consecutive additions for chemical homogenization.
  • medals were cast and analysed thereafter by means of spark emission spectrometry.
  • the melt was subjected to degassing by using N 2 during approximately 20 minutes.
  • the effectiveness of degassing was checked by means of Reduced Pressure or Straube-Pfeiffer Test where samples for alloy density evaluation were taken after degassing. In all cases, a minimum density of 2.65 gr/cm 3 was obtained in samples solidified in vacuum.
  • the metal liquid was poured into chemically bonded sand moulds, at temperatures between 710 y 740 oC, in order to obtain tensile test specimens (norm UNE-EN-ISO 6892-1).
  • the tensile test specimens ( Figure 2 ) were subjected to a T6 heat treatment in a laboratory furnace with a temperature control of ⁇ 2 oC.
  • the sequences of this thermal process were the following:
  • microstructures of the cast alloys were examined using optical and scanning electron microscopy: grain size, modification rate, iron rich phases and porosity have been evaluated in the tensile casting, see example in Figure 3 .
  • the Figure 4 shows different morphologies of iron phases observed in recycled aluminium alloys by using optical microscopy. Iron is known to be the most common and at the same time most detrimental impurity in aluminium alloys since it causes hard and brittle iron-rich intermetallic phases to precipitate during solidification. The most detrimental phase in the microstructure is the beta-phase of the Al 5 FeSi- type because of its platelet-shape, see Figure 4a ). This figure shows a typical ⁇ -A 5 FeSi phase with a monoclinic crystal structure and plate like morphology. Such platelets may have an extension of several millimetres and appear as needles in micrographic sections.
  • aluminium alloys with Mn, Cr and V additions do not present interactions with TiB master alloys (grain refiner agent) and Sr additions (modification of Si eutectic phases), obtaining good levels of grain refinement, Si modification and hydrogen degassing.
  • the Figure 5 shows micrographs which correspond to aluminium alloys: a) without alloying additions (Mn, Cr, V) and b) with the additions of Mn + Cr and c) with the addition of Mn, Cr and V. From results it can be seen that in b) and c) no platelet-shape phases (beta-phases) were found when performing the aforementioned additions in the conditions previously described in opposition to a) where these platelet-shape phases can be clearly observed (see arrows pointing thereto).
  • beta phase morphology (platelet-shape) is modified with the additions of Mn plus Cr or Mn plus Cr plus V, obtaining phases with a globular/chinese script morphology less harmful to mechanical properties.

Landscapes

  • 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)
  • Manufacture And Refinement Of Metals (AREA)
  • Continuous Casting (AREA)

Abstract

The present invention relates to iron containing aluminium alloys free of primary platelet-shaped beta-phase of the Al5FeSi-type in the solidified structure presenting the following chemical composition (in weight %): Si: 6.00 - 9.50; Fe: 0.15 - 0.60; Mn: 0.04 - 0.60; Mg: 0.20 - 0.70; Cr:0.01 - 0.60; Ti: 0.05 - 0.30; Sr and/or Na: 0.001 - 0.25; V:0.00 - 0.60; Cu:0.01 - 0.25; Ni: 0.01 - 0.1; Zn: 0.01 - 0.1; the balance being Al and incidental impurities. The present invention relates also to a process for the preparation of this aluminium alloy and aluminium alloy casting for example as components in aeronautic, automotive and energy industry.

Description

    FIELD OF THE INVENTION
  • The present invention relates to aluminium alloys, more particularly, it relates to aluminium alloy castings suitable as components for instance for vehicles, machines and electric applications which are required to have high strength and high elongation values among other properties. The present invention also relates to a process for its preparation from recycled aluminium alloys in order to obtain recycled aluminium casting free of platelet-shaped beta-phases.
    • BACKGROUND OF THE INVENTION
  • Aluminium alloys are widely used in diverse applications for instance as components in the automotive, aerospace, industrial machines, electric applications etc., because of their excellent mechanical properties as well as other technological properties such as corrosion resistance and reduced hot cracking tendency.
  • For the manufacturing of aluminium alloys there are basically two different methods which differ in the raw material: the primary production (primary alloy) which is of minerals rich in aluminium (bauxite) and aluminium recycling (secondary alloy) whose raw material is dross and other residues rich in aluminium.
  • The primary alloy production consists basically in reducing the oxide present in bauxite enhancing the purity of aluminium by electrolysis. The most important drawback of this method is the high quantity of energy (from 14 to 15 Kwh/kg) which is necessary to produce aluminium whereas in the aluminium recycling method the costs are about 0,5-0,75 Kwh/kg, that is lower than 5% of the primary production.
  • AlSiMg alloys are nowadays one of the most common aluminium castings alloys for high safety parts, such as automotive or aerospace components, which require high mechanical properties. This alloy presents also high ductility due to the low content in impurities and to the addition of elements such as Ti or Sr which refine and modify the microstructure, respectively. AlSiMg alloys are broadly used for castings produced in sand, permanent and investment moulds.
  • The high content in impurities, especially the high iron content, in secondary alloys (recycled aluminium) is considered as the main disadvantage. The iron content increases in recycled aluminium after each subsequent melting; its elimination or reduction is technically very complex and rather expensive, not being economically feasible.
  • The microstructure of AlSiMg alloys presents alpha aluminium dendrites and Al-Si eutectic and other intermetallic phases among which the iron-rich ones can be highlighted. Iron is well known for being the most common and detrimental impurity in aluminium alloys for mechanical properties, promoting the appearance of hard and brittle intermetallic iron-rich phases during solidification. The platelet-shaped beta phase (Al5FeSi) is the most prejudicial since it is well known that ductility and toughness are significantly decreased. Therefore, there has been recently an increasing interest in developing methods for producing improved recycled aluminium alloys in which the formation of the beta phase is reduced and the mechanical properties are thus improved.
  • Among the different methods mentioned before the chemical neutralization is the most used technique so far. The strategy was based on the inhibition of the platelet morphology by promoting the precipitation of the Al15Fe3Si2-type phase with the addition of a neutralizing element (Mn, Cr, Co and Be) and in some case controlling the condition of crystallization.
  • Other methods are based on the selection of raw materials with low iron content or on dilution with pure primary aluminium. Other methods relate to sweat melting and sedimentation of iron rich intermetallic phases by the so called sludge. However, all these methods result in considerable aluminium losses (about 10%) and are therefore unacceptable.
  • The patent WO 97/13882 discloses a method for producing iron-containing AlSi-alloys in particular Al-Si-Mn-Fe- alloys. The mechanical properties of aforementioned Al-alloys with iron contents between 0,4 and 2.0 wt.% can be improved by controlling the morphology of the iron containing intermetallic precipitates. The precipitation of platelet-shaped beta phase (β-Al5FeSi) has been found to be suppressed by a primary precipitation of the hexagonal Al8Fe2Si-type phase which is in turn less harmful one. The method comprises further controlling the condition of the crystallization by the addition of one or more elements such as Ti, Zr, Sr, Na and Ba.
  • In spite of the variety of methods in the state of the art, there is still the necessity of providing a method for obtaining recycled aluminium castings with mechanical properties close to those obtained in primary alloys, but at much lower production costs. The method is based on obtaining free platelet-shaped beta-phases aluminium castings by using recycled aluminium with high iron content.
    • BRIEF DESCRIPTION OF THE FIGURES
    • Figure 1. Table showing the chemical composition of AlSi7Mg alloys with additions of Mn, Cr and V to recycled ingots (Base Composition).
    • Figure 2: Tensile test casting used to evaluate the mechanical properties.
    • Figure 3: General view of secondary AlSi7Mg alloy with Mn, Cr and V additions, correctly degasified, not presenting porosity.
    • Figure 4: Optical micrographs showing iron-rich intermetallic phases: a) platelet-shape β-Al5FeSi phase in a secondary AlSi7Mg alloy without Mn, Cr or V additions, b) α-phases with globular shape in a secondary AlSi7Mg alloy with Mn, Cr and V additions.
    • Figure 5: Backscattered electron images and EDX spectrum of three different secondary AlSi7Mg alloy showing the different intermetallic iron rich precipitates (β-Al5FeSi, α-Al15(Fe,Mn,Cr,V)3Si2) depending on the alloying element added (Mn, Cr, V); a) without alloying elements; b) with Mn and Cr additions and c) with Mn, Cr and V additions.
    DESCRIPTION OF THE INVENTION
  • One aspect of the present invention refers to an iron containing aluminium alloy, hereinafter referred to as the alloy of the invention, which is free from primary platelet-shaped beta-phase of the Al5FeSi-type in the solidified structure presenting the following compositions (amounts expressed in weight percentage, wt.% in respect to the total weight of the alloy):
    Si 6.00 - 9.50
    Fe 0.15 - 0.60
    Mn 0.04 - 0.60
    Mg 0.20 - 0.70
    Cr 0.01 - 0.60
    Ti 0.05 - 0.30
    Sr and/or Na 0.001 - 0.25
    V 0.00 - 0.60
    Cu 0.01 - 0.25
    Ni 0.01 - 0.1
    Zn 0.01 - 0.1
  • the balance being Al and incidental impurities.
  • In a particular embodiment the iron-containing aluminium alloy of the invention presents a composition characterized in that the amount of Mn plus Cr in weight percentage is equal or larger than 50 % of Fe amount.
  • In another particular embodiment the iron-containing aluminium alloy of the invention presents a composition characterized in that the amount of Mn plus Cr plus V in weight percentage is equal or larger than 50 % of Fe amount.
  • In a further particular embodiment the iron-containing aluminium alloy of the invention presents a Fe content between 0.15 - 0.40% in weight percentage and an amount of Mn plus Cr plus V comprised between 0.15 - 0.40 wt.%.
  • In another aspect the present invention refers to a process for the preparation of the aluminium alloy of the invention comprising the following steps:
    1. a) Melting a secondary AlSi7Mg ingot from recycled aluminium.
    2. b) Adding the alloying elements:
      1. (i) Mn + Cr or
      2. (ii) Mn+Cr+V
        in suitable amounts
    3. c) Adding a grain refiner and a eutectic silicon modification agent.
    4. d) Submitting the molten alloy obtained in step c) to a degassing process.
    5. e) Introducing the degassed molten alloy in a mould.
    6. f) Casting solidification inside the mould.
    7. g) Casting extraction from the mould.
  • During the melting process of secondary ingots, due to the humidity of both the ingots and ambient itself, and also due to the affinity of the aluminium for oxygen, Al2O3 and H2 are formed. The alumina originated by this way becomes part of the dross and the free hydrogen is dissolved into the melt. The presence of hydrogen generates pores in the solidified castings reducing the ductility and strength. Therefore, the process of the invention comprises the degassing process according to already known methods such as treating the molten alloy with dry nitrogen or dry argon until the hydrogen content dissolved in the melt is low enough.
  • The process comprises the addition of alloying elements added as pure elements or as master alloys. The present invention resides in the addition of alloying elements: Mn+Cr o Mn+Cr+V, to the base composition of a secondary AlSi7Mg ingot of second fusion (or recycled aluminium).
  • The process comprises the addition of grain refiner and eutectic modification agents by means of master alloys additions. The modifier agent Na or Sr are the most common ones and are added to achieve the modification of the eutectic Al-Si structure, which precipitates during solidification, showing a rounded morphology instead of needle structure, typical when such a modifying agent is not added. It is well known that the presence of such needle structures reduces the mechanical properties (ductility, strength) of the alloys, promoting the appearance of cracks. In the case of refining agents, TiB master alloys are used to obtain a microstructures which shows a fine grain size and thus improving the final mechanical properties and also, reducing the porosity tendency.
  • According to the process for the preparation of the aluminium alloy of the invention, the platelet-shaped beta phases (Al5FeSi), so detrimental for the final mechanical properties, disappear and are substituted by globular-shaped alpha-phases (Al8Fe2Si) obtaining a substantial improvement in mechanical properties (Tensile strength, yield stress and elongation). The properties of the recycled alloys obtained according to the process of the present invention show mechanical properties comparable to those obtained in primary alloys.
  • In step e), the degassed molten alloy is poured into a sand and permanent mould. After filling the mould the cast alloy solidifies and an aluminium casting is obtained.
  • The aluminium alloys used in high responsibility castings need to fulfil certain mechanical and technological properties. For this reason, these parts are generally submitted to a T6 heat treatment. Another aspect of the present invention relates to a process for making an aluminium alloy casting which comprises submitting the solidified casting as described above to a T6 heat treatment. A T6 treatment comprises a first step of solution heat treatment, heating the castings at a temperature between 500 to 600ºC for 2 to 6 hours, followed by quenching. The second step will consist in an artificial aging at a temperature between 150 to 180ºC for 2 to 8 hours.
  • In a further aspect of the invention refers to an aluminium alloy casting obtainable by the above defined process presenting a tensile strength between 250-300 MPa, a yield strength between 190-230 MPa and elongation values between 4,5-9%.
  • The aluminium alloy casting of the invention can be used as a component for transport components such as wheels, suspension parts, brake parts, and energetic industry components.
  • A further aspect of the invention relates to a component made from recycled aluminium alloy castings such as steering knuckle, master cylinder and brake calliper.
  • According to the invention tensile test specimen are poured in sand mould and permanent moulds from the aluminium alloy of the invention with additions of Mn, Cr and V. The mechanical properties were determined with tensile test specimen according to norm (UNE UNE-EN_1706), (see fig 2). The aluminium alloys present a tensile strength of at least 250 MPa, a yield strength of at least 190 MPa and an elongation of at least 4.5 %. The test pieces according to the invention were submitted to microstructural analysis. The inventors found that the addition of controlled amounts of Mn, Cr and V according to the present invention eliminates the platelet-shape beta-phases (Al5FeSi).
  • On the other hand no interactions have been observed between the additions of Mn, Cr and V and structure modifying elements, such as Ti, B, Na and Sr. No differences have been observed in the grain refinement and Al-Si eutectic modification, with or without additions of Mn, Cr, V. There has not been observed either any interferences of the Mn, Cr, V elements with the conventional degassing method.
  • According to the scope of the invention, besides the additions of Mn, Cr and V other elements may be added for other purposes, without affecting the modification characteristics of the iron phases due to the presence of these elements.
  • The foregoing is illustrative of the present invention. However, this invention is not limited to the following precise embodiments described herein, but encompasses all equivalent modifications within the scope of the claims which follow.
    • EXAMPLES Example 1. Process for preparation of aluminium alloys and castings
  • The aluminium alloys have been produced by using secondary AlSi7Mg ingots, obtained from scrap, recycled aluminium dross and other metal residues rich in aluminium. The following table shows the chemical compositions of recycled ingots used in the examples, with iron contents between 0.28 and 0.34 wt.%. Three recycled ingots (ref. I, II and III) have been used in the experimental tests (Base Composition) are shown, the rest being Al:
    Ingot Secondary AlSi7Mg alloy Chemical Composition (wt.%)
    Si Fe Cu Mn Mg Cr Ni Zn Ti Sr V
    Ref. I 7.11 0.34 0.06 0.09 0.27 0.017 0.01 0.07 0.07 0.005 <0.01
    Ref. II 6.94 0.28 0.04 0.04 0.28 0.004 0.00 0.04 0.14 <0.003 <0.01
    Ref. III 6.92 0.28 0.04 0.04 0.25 <0.01 0.01 0.04 0.16 <0.003 <0.01
    Aluminium in balance
  • The recycled ingots were melted in an electric furnace (capacity of 50 kg of molten aluminium) at 710-750ºC. The melt was then alloyed and liquid treated according to the predetermined following schedule:
    1. 1. Ti was added to the melt (only to the melt of Ref I) in the form of TiB master alloys (5%Ti-1% B) in order to adjust the Ti content between 0.15 - 0.20 wt.%.
    2. 2. Thereafter Mn, Cr, V were added by using master alloys. The specific quantities of the alloying elements were added using master alloys:
      • o By using Mn-90 wt.% (Al-10 wt.%).
      • o By using Cr-80 wt.% (Al-20 wt.%).
      • o By using V-10 wt.% (Al-90 wt.%).
    3. 3. Finally, Sr-10% master alloy was added to the melt to adjust the Sr content between 0.005-0.025% Sr; and Mg was added in order to adjust its content between 0.25 - 0.70% Mg in agreement with the norm UNE-EN 1706 (AlSi7Mg).
  • The melt was held for 10 minutes between consecutive additions for chemical homogenization.
  • In order to determine the composition of the alloys that had been produced, medals were cast and analysed thereafter by means of spark emission spectrometry.
  • Once the aluminium alloys were tested to have the correct chemical compositions, (see Table in Figure 1), the melt was subjected to degassing by using N2 during approximately 20 minutes. The effectiveness of degassing (the presence of hydrogen in aluminium) was checked by means of Reduced Pressure or Straube-Pfeiffer Test where samples for alloy density evaluation were taken after degassing. In all cases, a minimum density of 2.65 gr/cm3 was obtained in samples solidified in vacuum.
  • Then, the next step was as follows: The metal liquid was poured into chemically bonded sand moulds, at temperatures between 710 y 740 ºC, in order to obtain tensile test specimens (norm UNE-EN-ISO 6892-1).
  • The tensile test specimens (Figure 2) were subjected to a T6 heat treatment in a laboratory furnace with a temperature control of ± 2 ºC. The sequences of this thermal process were the following:
    1. 1. Solution heat treatment for 7.5 h at 540 ºC,
    2. 2. After solution heat treatment, the samples were quenched in water at room temperature,
    3. 3. Alter quenching; the final step is the artificial aging of the samples for 5.5h at 155ºC.
  • The microstructures of the cast alloys were examined using optical and scanning electron microscopy: grain size, modification rate, iron rich phases and porosity have been evaluated in the tensile casting, see example in Figure 3.
  • The Figure 4 shows different morphologies of iron phases observed in recycled aluminium alloys by using optical microscopy. Iron is known to be the most common and at the same time most detrimental impurity in aluminium alloys since it causes hard and brittle iron-rich intermetallic phases to precipitate during solidification. The most detrimental phase in the microstructure is the beta-phase of the Al5FeSi- type because of its platelet-shape, see Figure 4a). This figure shows a typical β-A5FeSi phase with a monoclinic crystal structure and plate like morphology. Such platelets may have an extension of several millimetres and appear as needles in micrographic sections. In order to avoid the platelet morphology, chemical neutralization (additions of MnCrV or MnCr) are used according to the present invention which have been shown to inhibit this beta morphology promoting the precipitation of α-Al15(Fe,Mn,Cr,V)3Si2 with globular/chinese script morphology, as shown in Figure 4.b), containing substantial amounts of alloying elements (Mn, Cr, V).
  • The aluminium alloys with Mn, Cr and V additions do not present interactions with TiB master alloys (grain refiner agent) and Sr additions (modification of Si eutectic phases), obtaining good levels of grain refinement, Si modification and hydrogen degassing.
    • Example 2. Effect of different quantities of alloying elements (Mn,Cr,V)
  • When the content of the rest of chemicals elements keep constant, it is possible to study el effect of Mn, Cr and V by varying the content of these latter ones. Several chemical compositions were prepared in accordance with the present invention, see Table in Figure 1.
  • In order to determine the effectiveness of beta-phases modification, metallographic analyses were performed in all the tensile specimens. Optical microscopy and scanning electron microscopy, SEM, were used. The preparation procedure consisted of sectioning, grinding and polishing of the specimens.
  • The Figure 5 shows micrographs which correspond to aluminium alloys: a) without alloying additions (Mn, Cr, V) and b) with the additions of Mn + Cr and c) with the addition of Mn, Cr and V. From results it can be seen that in b) and c) no platelet-shape phases (beta-phases) were found when performing the aforementioned additions in the conditions previously described in opposition to a) where these platelet-shape phases can be clearly observed (see arrows pointing thereto). Therefore, with the obtained results, it is possible to conclude that the beta phase morphology (platelet-shape) is modified with the additions of Mn plus Cr or Mn plus Cr plus V, obtaining phases with a globular/chinese script morphology less harmful to mechanical properties.
    • Example 3. Mechanical Properties Evaluation
  • In order to characterize the mechanical properties of aluminium cast alloys according to the invention, tensile test specimens were tested at room temperature in accordance with the method established in the norm UNE-EN-ISO 6892-1. Tensile tests were carried out using an Instron Universal testing machine to obtain yield strength (R 0,2, MPa), ultimate stress (R m, MPa) and elongation percentage (%). From tensile tests, the following yield strength, ultimate stress and elongation have been achieved:
    • Yield strength, R 0.2 = 200 MPa.
    • Ultimate stress, R m = 274 MPa.
    • Elongation = 8.5 %.

Claims (10)

  1. An iron containing aluminium alloy free of primary platelet-shaped beta-phase of the Al5FeSi-type in the solidified structure presenting the following composition (amounts expressed in % by weight in respect to the total weight of the alloy): Si 6.00 - 9.50 Fe 0.15 - 0.60 Mn 0.04 - 0.60 Mg 0.20 - 0.70 Cr 0.01 - 0.60 Ti 0.05 - 0.30 Sr and/or Na 0.001 - 0.25 V 0.00 - 0.60 Cu 0.01 - 0.25 Ni 0.01 - 0.1 Zn 0.01 - 0.1
    balance being Al and incidental impurities.
  2. An iron-containing aluminium alloy according to claim 1, presenting a composition characterized in that the total amount of Mn and Cr in weight percentage (wt.%) is equal or larger than 50 % of the Fe amount.
  3. An iron-containing aluminium alloy according to claim 1, presenting a composition characterized in that the total amount of Mn, Cr and V in weight percentage (wt.%) is equal or larger than 50 % of the Fe amount.
  4. An iron-containing aluminium alloy according to claim 1, presenting a Fe content of 0.15 - 0.40% by weight and an amount of Mn, Cr and V taken together which is comprised between 0.15 - 0.40 % by weight.
  5. A process for the preparation of the aluminium alloy of claims 1 to 4, comprising the following steps:
    a) Melting a secondary AlSi7Mg ingot from recycled aluminium.
    b) Adding the alloying elements:
    (i) Mn + Cr or
    (ii) Mn+Cr+V
    in suitable amounts
    c) Adding a grain refiner and a eutectic silicon modification agent
    d) Submitting the molten alloy obtained in step c) to a degassing process
    e) Introducing the degassed molten alloy in a mould
    f) Casting solidification inside the mould
    g) Casting extraction from the mould.
  6. A process according to claim 5, wherein the alloying elements are added as pure elements or as master alloys.
  7. A process for making an aluminium alloy casting which comprises submitting a solidified casting as obtained according to the process of claims 5 or 6, to a T6 heat treatment.
  8. An aluminium alloy casting presenting tensile strength between 250-300 MPa, a yield strength between 190-230 MPa and elongation values between 4,5-9% obtainable by the process of claim 7.
  9. Use of the aluminium alloy casting of claim 8, as a component for transport components selected from wheels, suspension parts and brake parts, or as a component for energetic industry.
  10. A component made from the aluminium alloy casting of claim 8, selected from steering knuckle, master cylinder and brake calliper.
EP20100382360 2010-12-28 2010-12-28 Method for obtaining improved mechanical properties in recycled aluminium castings free of platelet-shaped beta-phases Active EP2471967B1 (en)

Priority Applications (3)

Application Number Priority Date Filing Date Title
EP20100382360 EP2471967B1 (en) 2010-12-28 2010-12-28 Method for obtaining improved mechanical properties in recycled aluminium castings free of platelet-shaped beta-phases
ES10382360.5T ES2507865T3 (en) 2010-12-28 2010-12-28 Method to obtain improved mechanical properties in plate-shaped beta-free recycled aluminum molds
PCT/ES2011/070911 WO2012089886A2 (en) 2010-12-28 2011-12-28 Method for obtaining improved mechanical properties in recycled aluminum castings free of beta phases in the form of a sheet

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP20100382360 EP2471967B1 (en) 2010-12-28 2010-12-28 Method for obtaining improved mechanical properties in recycled aluminium castings free of platelet-shaped beta-phases

Publications (2)

Publication Number Publication Date
EP2471967A1 true EP2471967A1 (en) 2012-07-04
EP2471967B1 EP2471967B1 (en) 2014-07-09

Family

ID=44279841

Family Applications (1)

Application Number Title Priority Date Filing Date
EP20100382360 Active EP2471967B1 (en) 2010-12-28 2010-12-28 Method for obtaining improved mechanical properties in recycled aluminium castings free of platelet-shaped beta-phases

Country Status (3)

Country Link
EP (1) EP2471967B1 (en)
ES (1) ES2507865T3 (en)
WO (1) WO2012089886A2 (en)

Cited By (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103290277A (en) * 2013-05-23 2013-09-11 宁国市锦泰高科铝业有限责任公司 High-purity high-strength aluminum alloy for ship cooling system and preparation method thereof
CN105063392A (en) * 2015-08-13 2015-11-18 安徽优合铝业科技有限公司 Hub casting and forming technology
EP3124632A1 (en) * 2015-07-28 2017-02-01 Univerzita J. E. Purkyne v Usti nad Labem Aluminum alloy, in particular for the production of mould segment castings for forming tyres, and the method of heat treatment of mould segment castings.
US20170121793A1 (en) * 2015-04-15 2017-05-04 Daiki Aluminium Industry Co., Ltd. Aluminum alloy for die casting, and aluminum alloy die cast produced using same
WO2017165962A1 (en) * 2016-03-31 2017-10-05 Rio Tinto Alcan International Limited Aluminum alloys having improved tensile properties
CN110121566A (en) * 2016-12-22 2019-08-13 Ksm铸造集团有限公司 Ceralumin
WO2019217319A1 (en) * 2018-05-07 2019-11-14 Alcoa Usa Corp. Al-Mg-Si-Mn-Fe CASTING ALLOYS
CN110923487A (en) * 2019-12-11 2020-03-27 苏州大学 Method for separating Fe element from aluminum alloy waste
DE102019205267B3 (en) * 2019-04-11 2020-09-03 Audi Ag Die-cast aluminum alloy
CN111719068A (en) * 2020-05-30 2020-09-29 苏州慧金新材料科技有限公司 Alloy material for mobile phone middle plate and preparation method and application thereof
CN113215455A (en) * 2021-05-11 2021-08-06 苏州菲姆卡金属科技有限公司 High-quality secondary aluminum and preparation method thereof
US11214496B2 (en) 2016-03-29 2022-01-04 Tosoh Corporation Electrolytic manganese dioxide and method for its production, and its application
CN115125418A (en) * 2021-03-26 2022-09-30 本田技研工业株式会社 Aluminum alloy, method for producing layered structure, and layered structure
DE102021129329A1 (en) 2021-11-11 2023-05-11 Bayerische Motoren Werke Aktiengesellschaft Process for producing an aluminum alloy and component
CN116403755A (en) * 2023-04-12 2023-07-07 北京理工大学 High-strength high-conductivity regenerated aluminum alloy wire and preparation method thereof
EP4273286A1 (en) * 2022-05-05 2023-11-08 Nio Technology (Anhui) Co., Ltd Aluminum alloy and component part prepared therefrom
US20230407446A1 (en) * 2022-06-21 2023-12-21 GM Global Technology Operations LLC Trace element modification of iron-rich phase in aluminum-silicon alloys to accommodate high iron content

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN115927925A (en) * 2021-09-24 2023-04-07 通用汽车环球科技运作有限责任公司 Low-carbon footprint cast aluminum component
CN115323208B (en) * 2022-08-16 2023-06-02 沈阳西蒙科技有限公司 Low-hydrogen and low-slag-inclusion cast structural member and casting production method thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997013882A1 (en) 1995-10-10 1997-04-17 Opticast Ab A METHOD OF REDUCING THE FORMATION OF PRIMARY PLATLET-SHAPED BETA-PHASE IN IRON CONTAINING AlSi-ALLOYS, IN PARTICULAR IN Al-Si-Mn-Fe ALLOYS
JPH1112705A (en) * 1997-06-20 1999-01-19 Sumitomo Light Metal Ind Ltd Production of high strength aluminum alloy forging excellent in machinability
EP0997550A1 (en) * 1998-10-05 2000-05-03 Alusuisse Technology &amp; Management AG Method for fabricating a component from an aluminium alloy by pressure die-casting
WO2005071127A1 (en) * 2004-01-09 2005-08-04 Alcoa Inc. Al-si-mn-mg alloy for forming automotive structural parts by casting and t5 heat treatment
US20090297393A1 (en) * 2006-07-14 2009-12-03 Bdw Technologies Gmbh Aluminum alloy and the utilization thereof for a cast component, in particular a motor vehicle

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1997013882A1 (en) 1995-10-10 1997-04-17 Opticast Ab A METHOD OF REDUCING THE FORMATION OF PRIMARY PLATLET-SHAPED BETA-PHASE IN IRON CONTAINING AlSi-ALLOYS, IN PARTICULAR IN Al-Si-Mn-Fe ALLOYS
JPH1112705A (en) * 1997-06-20 1999-01-19 Sumitomo Light Metal Ind Ltd Production of high strength aluminum alloy forging excellent in machinability
EP0997550A1 (en) * 1998-10-05 2000-05-03 Alusuisse Technology &amp; Management AG Method for fabricating a component from an aluminium alloy by pressure die-casting
WO2005071127A1 (en) * 2004-01-09 2005-08-04 Alcoa Inc. Al-si-mn-mg alloy for forming automotive structural parts by casting and t5 heat treatment
US20090297393A1 (en) * 2006-07-14 2009-12-03 Bdw Technologies Gmbh Aluminum alloy and the utilization thereof for a cast component, in particular a motor vehicle

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
KOCH H ET AL: "Eisenarme Aluminium-Druckgusslegierungen als Substitutionswerkstoff fuer Stahlblechkonstruktionen im Automobilbau // Low-iron aluminum die cast alloys as substitute material for steel sheet constructions in automobile manufacture", GIESSEREIPRAXIS, FACHVERLAG SCHIELE UND SCHON GMBH, BERLIN, DE, no. 4, 1 January 2000 (2000-01-01), pages 148 - 152, XP009099393, ISSN: 0016-9781 *
KOPPER, ADAM ET AL: "Solder resistance mechanisms of novel Al-Sr-Si die casting alloys", LIGHT METALS (WARRENDALE, PA, UNITED STATES) 801-805 CODEN: LMPMDF; ISSN: 0147-0809, 2006, XP009150752 *

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103290277A (en) * 2013-05-23 2013-09-11 宁国市锦泰高科铝业有限责任公司 High-purity high-strength aluminum alloy for ship cooling system and preparation method thereof
US20170121793A1 (en) * 2015-04-15 2017-05-04 Daiki Aluminium Industry Co., Ltd. Aluminum alloy for die casting, and aluminum alloy die cast produced using same
EP3124632A1 (en) * 2015-07-28 2017-02-01 Univerzita J. E. Purkyne v Usti nad Labem Aluminum alloy, in particular for the production of mould segment castings for forming tyres, and the method of heat treatment of mould segment castings.
CN105063392A (en) * 2015-08-13 2015-11-18 安徽优合铝业科技有限公司 Hub casting and forming technology
US11214496B2 (en) 2016-03-29 2022-01-04 Tosoh Corporation Electrolytic manganese dioxide and method for its production, and its application
WO2017165962A1 (en) * 2016-03-31 2017-10-05 Rio Tinto Alcan International Limited Aluminum alloys having improved tensile properties
US11198925B2 (en) 2016-03-31 2021-12-14 Rio Tinto Alcan International Limited Aluminum alloys having improved tensile properties
CN110121566A (en) * 2016-12-22 2019-08-13 Ksm铸造集团有限公司 Ceralumin
WO2019217319A1 (en) * 2018-05-07 2019-11-14 Alcoa Usa Corp. Al-Mg-Si-Mn-Fe CASTING ALLOYS
DE102019205267B3 (en) * 2019-04-11 2020-09-03 Audi Ag Die-cast aluminum alloy
CN110923487A (en) * 2019-12-11 2020-03-27 苏州大学 Method for separating Fe element from aluminum alloy waste
CN111719068A (en) * 2020-05-30 2020-09-29 苏州慧金新材料科技有限公司 Alloy material for mobile phone middle plate and preparation method and application thereof
CN115125418A (en) * 2021-03-26 2022-09-30 本田技研工业株式会社 Aluminum alloy, method for producing layered structure, and layered structure
CN113215455A (en) * 2021-05-11 2021-08-06 苏州菲姆卡金属科技有限公司 High-quality secondary aluminum and preparation method thereof
DE102021129329A1 (en) 2021-11-11 2023-05-11 Bayerische Motoren Werke Aktiengesellschaft Process for producing an aluminum alloy and component
EP4273286A1 (en) * 2022-05-05 2023-11-08 Nio Technology (Anhui) Co., Ltd Aluminum alloy and component part prepared therefrom
US20230407446A1 (en) * 2022-06-21 2023-12-21 GM Global Technology Operations LLC Trace element modification of iron-rich phase in aluminum-silicon alloys to accommodate high iron content
CN116403755A (en) * 2023-04-12 2023-07-07 北京理工大学 High-strength high-conductivity regenerated aluminum alloy wire and preparation method thereof

Also Published As

Publication number Publication date
EP2471967B1 (en) 2014-07-09
ES2507865T3 (en) 2014-10-15
WO2012089886A2 (en) 2012-07-05
WO2012089886A3 (en) 2012-12-13

Similar Documents

Publication Publication Date Title
EP2471967B1 (en) Method for obtaining improved mechanical properties in recycled aluminium castings free of platelet-shaped beta-phases
EP2350330B1 (en) Magnesium alloys containing rare earths
KR102609410B1 (en) die casting alloy
US7087125B2 (en) Aluminum alloy for producing high performance shaped castings
CN111032897A (en) Method of forming cast aluminum alloy
KR101124235B1 (en) Aluminium alloy and aluminium alloy casting
EP1882753A1 (en) Aluminium alloy
CN110714148A (en) High-performance semi-solid die-casting aluminum alloy and preparation method thereof
EP1882754B1 (en) Aluminium alloy
CN108396204B (en) Hypoeutectic aluminum-silicon alloy casting and process method for improving performance thereof
CN102912196A (en) Aluminum-silicon-magnesium cast aluminum alloy and manufacturing method thereof
GB2500825A (en) An Al-Mg-Si-Mn alloy and a method of producing such an alloy
CN107447142B (en) Tough high Alcoa of a kind of automobile height and preparation method thereof
CN108251714A (en) A kind of high tough aluminium alloy of extrusion casint and its extrusion casting method
CN113106306A (en) High-strength corrosion-resistant 5xxx series alloy and preparation method thereof
CN110218917B (en) Alloy aluminum bar containing rare earth elements and preparation process thereof
CN113584361B (en) High-strength corrosion-resistant 7-series aluminum alloy and casting method thereof
CN114457266A (en) Ultrahigh-strength and toughness cast aluminum alloy and forming method thereof
CN115418535B (en) Aluminum alloy material, preparation method and application thereof, and aluminum alloy product
KR101499096B1 (en) Aluminum alloy and manufacturing method thereof
US8016957B2 (en) Magnesium grain-refining using titanium
Haro et al. Influence of solutionising and aging temperatures on microstructure and mechanical properties of cast Al–Si–Cu alloy
KR100840385B1 (en) Heat resisting aluminum alloy
CN111118358A (en) Er-containing castable wrought Al-Cu alloy
CN115125422B (en) Corrosion-resistant high-strength-toughness Al-Li-Cu-Zr-Er alloy plate and preparation method thereof

Legal Events

Date Code Title Description
AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

AX Request for extension of the european patent

Extension state: BA ME

PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20121218

17Q First examination report despatched

Effective date: 20130219

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: CASA MARISTAS AZTERLAN

Owner name: BEFESA ALUMINIO, S.L.

INTG Intention to grant announced

Effective date: 20140211

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

REG Reference to a national code

Ref country code: GB

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: CH

Ref legal event code: EP

Ref country code: AT

Ref legal event code: REF

Ref document number: 676632

Country of ref document: AT

Kind code of ref document: T

Effective date: 20140715

REG Reference to a national code

Ref country code: IE

Ref legal event code: FG4D

REG Reference to a national code

Ref country code: DE

Ref legal event code: R096

Ref document number: 602010017334

Country of ref document: DE

Effective date: 20140821

REG Reference to a national code

Ref country code: ES

Ref legal event code: FG2A

Ref document number: 2507865

Country of ref document: ES

Kind code of ref document: T3

Effective date: 20141015

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 676632

Country of ref document: AT

Kind code of ref document: T

Effective date: 20140709

REG Reference to a national code

Ref country code: NL

Ref legal event code: VDEP

Effective date: 20140709

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: NO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20141009

Ref country code: FI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: BG

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20141009

Ref country code: PT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20141110

Ref country code: SE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: LT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: HR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: LV

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: AT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: NL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: CY

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: IS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20141109

Ref country code: PL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: RS

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602010017334

Country of ref document: DE

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PLBI Opposition filed

Free format text: ORIGINAL CODE: 0009260

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: RO

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: IT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: EE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: SK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: DK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: CZ

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

26 Opposition filed

Opponent name: TRIMET ALUMINIUM SE

Effective date: 20150407

PLAX Notice of opposition and request to file observation + time limit sent

Free format text: ORIGINAL CODE: EPIDOSNOBS2

26 Opposition filed

Opponent name: BORGWARNER, INC.

Effective date: 20150408

REG Reference to a national code

Ref country code: DE

Ref legal event code: R026

Ref document number: 602010017334

Country of ref document: DE

Effective date: 20150407

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20141231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: LU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20141228

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20141228

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PLAF Information modified related to communication of a notice of opposition and request to file observations + time limit

Free format text: ORIGINAL CODE: EPIDOSCOBS2

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20141228

Ref country code: LI

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20141231

Ref country code: IE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20141228

Ref country code: CH

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20141231

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SI

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

PLBB Reply of patent proprietor to notice(s) of opposition received

Free format text: ORIGINAL CODE: EPIDOSNOBS3

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 6

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: SM

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MC

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: BE

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: HU

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT; INVALID AB INITIO

Effective date: 20101228

Ref country code: MT

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

Ref country code: TR

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 7

PLCK Communication despatched that opposition was rejected

Free format text: ORIGINAL CODE: EPIDOSNREJ1

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE PATENT HAS BEEN GRANTED

APBM Appeal reference recorded

Free format text: ORIGINAL CODE: EPIDOSNREFNO

APBP Date of receipt of notice of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA2O

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO

APBM Appeal reference recorded

Free format text: ORIGINAL CODE: EPIDOSNREFNO

APBP Date of receipt of notice of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA2O

APBQ Date of receipt of statement of grounds of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA3O

APBQ Date of receipt of statement of grounds of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA3O

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 8

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: MK

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: AL

Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT

Effective date: 20140709

REG Reference to a national code

Ref country code: FR

Ref legal event code: PLFP

Year of fee payment: 9

APBU Appeal procedure closed

Free format text: ORIGINAL CODE: EPIDOSNNOA9O

PLAY Examination report in opposition despatched + time limit

Free format text: ORIGINAL CODE: EPIDOSNORE2

PLBC Reply to examination report in opposition received

Free format text: ORIGINAL CODE: EPIDOSNORE3

PLAY Examination report in opposition despatched + time limit

Free format text: ORIGINAL CODE: EPIDOSNORE2

PLBC Reply to examination report in opposition received

Free format text: ORIGINAL CODE: EPIDOSNORE3

APBM Appeal reference recorded

Free format text: ORIGINAL CODE: EPIDOSNREFNO

APBP Date of receipt of notice of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA2O

APAH Appeal reference modified

Free format text: ORIGINAL CODE: EPIDOSCREFNO

APBQ Date of receipt of statement of grounds of appeal recorded

Free format text: ORIGINAL CODE: EPIDOSNNOA3O

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20230929

Year of fee payment: 14

APBU Appeal procedure closed

Free format text: ORIGINAL CODE: EPIDOSNNOA9O

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: ES

Payment date: 20240102

Year of fee payment: 14

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20231229

Year of fee payment: 14