EP1882754B1 - Aluminium alloy - Google Patents

Aluminium alloy Download PDF

Info

Publication number
EP1882754B1
EP1882754B1 EP07014135.3A EP07014135A EP1882754B1 EP 1882754 B1 EP1882754 B1 EP 1882754B1 EP 07014135 A EP07014135 A EP 07014135A EP 1882754 B1 EP1882754 B1 EP 1882754B1
Authority
EP
European Patent Office
Prior art keywords
alloy
aluminium alloy
percent
aluminium
percentage
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.)
Not-in-force
Application number
EP07014135.3A
Other languages
German (de)
French (fr)
Other versions
EP1882754A1 (en
Inventor
Iñaki Landa Sastre
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.)
Fagor Electrodomesticos SCL
Edertek S Coop
Original Assignee
Fagor Electrodomesticos SCL
Edertek S Coop
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
Priority claimed from EP06015671A external-priority patent/EP1882753A1/en
Application filed by Fagor Electrodomesticos SCL, Edertek S Coop filed Critical Fagor Electrodomesticos SCL
Priority to EP07014135.3A priority Critical patent/EP1882754B1/en
Publication of EP1882754A1 publication Critical patent/EP1882754A1/en
Application granted granted Critical
Publication of EP1882754B1 publication Critical patent/EP1882754B1/en
Not-in-force legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/02Alloys based on aluminium with silicon as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22FCHANGING THE PHYSICAL STRUCTURE OF NON-FERROUS METALS AND NON-FERROUS ALLOYS
    • C22F1/00Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working
    • C22F1/04Changing the physical structure of non-ferrous metals or alloys by heat treatment or by hot or cold working of aluminium or alloys based thereon
    • C22F1/043Changing 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. Particularly, the present invention is directed to an aluminium alloy which exhibits suitable tensile strength, yield strength and elongation percentage for its use to manufacture vehicular suspension parts.
  • Aluminium alloys are widely used as materials for various components of vehicles, industrial machines, airplanes, electric appliances for domestic use and other apparatus of various types.
  • Such aluminium alloys there are cast aluminium alloys, a representative of which is A356.
  • Such cast aluminium alloys are used in important durable parts requiring higher mechanical properties such as vehicle components, metal fittings for stringing and components of hydraulic systems, and in like applications.
  • Typical mechanical property values of the A356 alloy as treated by a T6 heat treatment are 250 MPa tensile strength, 200 MPa yield strength and 5 % elongation.
  • the A356 alloy has widespread applications for structural components in the automotive, aerospace, and general engineering industries because of their excellent castability, corrosion resistance, and, particularly, high strength-to-weight ratio in the heat-treated condition.
  • microstructures of alloy A356 are comprised of an aluminium matrix, which is strengthened by MgSi precipitates and, to a far lesser extent, by Si precipitates, and a dispersion of eutectic Al-Si particles and Fe-rich intermetallics.
  • the variables affecting the microstructure mainly include composition, solidification conditions, and heat treatment.
  • composition of A356 alloy comprises the following components: 91 to 93 wt % of Al; 6.5 to 7.5 wt % of Si; 0.20 to 0.40 wt % of Mg; 0 to 0.02 wt % of Cu; 0 to 0.20 wt % of Fe; 0 to 0.10 wt % of Mn; 0 to 0.20 wt % of Ti; and 0 to 0.10wt%ofZn.
  • Another known aluminium die casting alloys for automotive structural applications have silicon contents between about 9-11 % by weight.
  • these alloys include C448 and Silafont 36.
  • the high Si content of these alloys results in brittle Al-Si eutectic networks in the as-cast condition.
  • these alloys need a high temperature solution heat treatment that serves, principally, to break down the eutectic network and to spheroidize the Si particles.
  • the solution heat treatment increases costs and also introduces part distortion which requires straightening or machining, which adds cost in the manufacturing process.
  • US 6364970 is directed to a hypoeutectic aluminium-silicon alloy.
  • the alloy according to the US 6364970 patent also known in industry as Silafont 36, contains an iron content of up to 0.15% by weight and a strontium refinement of 30 to 300 ppm (0.003 to 0.03% by weight). It has a high fracture strength resulting from the refined eutectic silicon phase and resulting from the addition of Sr to the alloy.
  • the alloy further contains 0.5 to 0.8% by weight manganese (Mn).
  • a material used for a vehicular suspension part such as a steering knuckle and a suspension arm is required to have high tensile strength, high yield strength, sufficient elongation percentage, as well as other technological properties such as corrosion resistance, low hot cracking, etc. Accordingly, it is desirable to provide an aluminium alloy with said properties.
  • the aluminium casting alloy Anticorodal-78 dv with a chemical composition in wt % of 6.5-7.5 % Si, up to 0.15 % Fe, up to 0.02 % Cu, up to 0.05 % Mn, 0.30-0.45 % Mg, up to 0.07 % Zn, 0.10-0.18 % Ti in addition of Sr and the balance Al, is described in "Hüttenaluminium Gusslegtechniken” 1994, Aluminium Rheinfelden GMGH.
  • the Anticorodal-78 dv alloy does not contains silver nor rare earth elements.
  • EP1657319 describes AlSi7Mg and AlSi7MgCu alloys with the addition of 0.1-1.0 % Ag.
  • the AlSi7Mg alloy herein described does not contain any strontium content. It is disclosed that the addition of silver, have no significant effect on the mechanical properties of the AlSi7Mg alloy.
  • the problem to be solved by the present invention is to provide an aluminium alloy with improved mechanical and technological properties suitable for vehicular suspension parts.
  • the solution is based on that the present inventors have found that an aluminium modified alloy containing silver and strontium in suitable amounts obtained by the process of the present invention, has an improved tensile strength, yield strength, and elongation percentage, and also suitable technological properties such as corrosion resistance and low hot cracking, compared to A356 aluminium alloy.
  • novel alloy of the present invention make it particularly suitable for durable components requiring higher mechanical properties such as vehicle components, particularly for suspension vehicle components such as steering knuckles and suspension arms. Furthermore, the new alloy is low in cost.
  • an aspect of the invention relates to an aluminium alloy according to claim 1.
  • Another aspect of the invention relates to a process of making an aluminium alloy according to claim 7.
  • Another aspect of the present invention relates to the use of the aluminium alloy casting described herein, as a vehicular suspension component according to claim 11.
  • vehicular suspension components such as steering knuckle and a suspension arms
  • a vehicular suspension component according to claim 13 which is made from an aluminium alloy casting as described herein.
  • the precipitation hardening elements included in the alloy magnesium (Mg) and silicon (Si), are more finely dispersed in the alloy and precipitate.
  • the chemical composition for the aluminium alloy according to the present invention consists essentially 6.5 to 7.5 percent silicon, 0.2 to 0.4 percent magnesium, 0.1 to 0.2 percent titanium (Ti), 0.05 to 0.3 percent silver, 0.002 to 0.04 percent strontium, and the balance comprising aluminium and unavoidable impurities.
  • the aluminium alloy contains between 0.02 to 0.04 percent strontium and between 0.1 to 0.25 percent silver. More preferably, more than 0.02 percent strontium up to 0.04 percent, and between 0.1 to 0.2 percent silver.
  • aluminium alloys wherein the content of strontium is 0.025, 0.03, 0.032, 0.035 or 0.04 percent.
  • the aluminium alloy contains, by percentage of weight, 0.2 percent silver.
  • the Ag is an essential element of the aluminium alloys of the present invention, due to its contribution to the increased fineness of the eutectic Si structure, the increased fineness of the needle iron (Fe) structure, and the increased uniformity and fineness of the precipitation hardening alloys of Mg, and Si which is suitable for improve the properties above mentioned.
  • the Ag content is at least 0.05 wt %.
  • Ti is an element added for making the grains of the casting finer to improve the mechanical properties and mainly the ductility of the part.
  • the Ti content is defined as within a range from 0.1 to 0.2 wt %.
  • Mg is an essential hardening agent developed after heat treatment in Al-Si alloys.
  • the hardening phase Mg 2 Si is limited by solubility, which corresponds approximately until 0.7 % wherein maximum hardness is reached.
  • the Mg content is defined as within a range from 0.2 to 0.4 wt %.
  • Si is an essential element depositing together with Mg as Mg 2 Si by artificial aging to provide high strength (yield strength) for final products upon use. Its addition improves the flowability (castability), the hot strength, and other properties of the alloy. Alloys with less than 12% of Si are referred to as hypoeutectic, those with close to 12% Si as eutectic, and those with over 12% Si as hypereutectic. Modification of hypoeutectic alloys ( ⁇ 12% Si) is particularly advantageous in sand castings and can be effectively achieved through the addition of a controlled amount of sodium or strontium, which refines the eutectic phase. In general, the optimum range of Si depends on the process, e.g.
  • Si in sand castings amounts between 5 to 7 wt %
  • die casting amounts between 7 to 9 wt %
  • high pressure die casting between 8 to 12 wt %.
  • the addition of Si not only improves the mechanical properties, but also reduces the density and thermal expansion rate.
  • the Si content is defined as within the range from 6.5 to 7.5 wt %.
  • the aluminium alloy further comprises, by percentage of weight, 0.1 to 0.6 % of rare earth elements. More preferably, the aluminium alloy contains, by percentage of weight, 0.4 % of rare earth elements.
  • said rare earth element is at least one element selected from the group comprising La, Ce, Pr, Nb, Pm, Sm, Eu, Ga, Tb, Dy, Ho, Er, Tm, Yb, Lu, Y, and Sc. More preferred are those selected from the group consisting of La, Ce, Pr and Nd. Generally, rare earth elements are eliminated as slag in refusions.
  • the aluminium alloy contains, by percentage of weight, between 0.05 and 0.2 percent silver and between 0.2 and 0.5 percent of rare earth elements. More preferably, between 0.1 and 0.2 percent silver and between 0.3 and 0.4 percent of rare earth elements. Particularly preferred are those wherein the content of silver is 0.1 percent and the content of rare earth elements is 0.4 percent.
  • rare earth elements By adding slight amounts of rare earth elements the casting defects of the aluminium alloy casting are reduced, increased uniformity of structure and increased fineness of dispersion are achieved, and the strength of the aluminium alloy casting is strikingly improved. Furthermore, presence of rare earth elements contributes to make the grain size of the casting finer improving its strength and ductility, and modifies the eutectic structure of Al-Si alloys. Another advantage of the presence of rare earth elements in the aluminium alloys of the present invention is that it reduces the costs, due to it permits to reduce the amount of Ag in the composition.
  • the alloys according to the present invention are substantially free of copper and iron.
  • substantially free means having no significant amount of that component purposely added to the alloy composition, it being understood that trace amounts of unavoidable impurities may find their way into a desired end product.
  • Copper substantially improves strength and hardness in the as-cast and heat-treated conditions. Alloys containing 4 to 6% Cu respond most strongly to thermal treatment. Copper generally reduces resistance to general corrosion and, in specific compositions and material conditions, stress corrosion susceptibility. Additions of copper also reduce hot tear resistance and decrease castability.
  • Iron improves hot tear resistance and decreases the tendency for die sticking or soldering in die casting. Increases in iron content are, however, accompanied by substantially decreased ductility. Iron reacts to form a myriad of insoluble phases in aluminium alloy melts, the most common of which are FeAl 3 , FeMnAl 6 and ⁇ -AlFeSi. These essentially insoluble phases are responsible for decrease in mechanical properties, such as elongation and tensile strength, especially at elevated temperature. As the fraction of insoluble phase increases with increased iron content, casting considerations as flowability and feeding characteristics are adversely affected. Iron participates in the formation of sludging phases with manganese, chromium and other elements.
  • the aluminium alloy of the present invention is substantially free of copper and iron, i.e. it has no significant amount of those components purposely added to the alloy composition, nevertheless it is understood that trace amounts of unavoidable impurities may find their way into a desired end product.
  • the content of iron in the aluminium alloys of the present invention is lower than 0.15 % wt.
  • the aluminium alloy described herein can be prepared by a process comprising (a) melting the raw materials, alloying elements and auxiliary materials in suitable amounts to obtain the composition and properties of interest; (b) undergone the molten alloy thus obtained to a degassing process, and (c) introducing (pouring) the molten metal in a mould and reduce the temperature until solidifying as rough casting parts.
  • the raw materials in solid state are introduced in the furnace as pure elements or as alloys of the components.
  • ingots of the aluminium alloy A356 basic composition
  • alloying elements are added, and then when the ingots are melt, the composition of the molten metal is analyzed and optionally, if necessary, the proportions of the components in the alloy are adjusted by adding suitable amounts of such components or alternatively diluted the molten by adding aluminium ingots and then adding suitable amounts of the components to adjust their proportion.
  • additives are added in order to achieve the suitable mechanical and technological properties.
  • additives are the modifying agent strontium and the refining agent titanium.
  • the modifying agent is used in order to achieve that the eutectic structure aluminium-silicon, which precipitates during the solidifying step of the part, shows a rounded shape, instead of a needle shape characteristic wherein no modifying is present.
  • the eutectic structure shows a needle shape, the mechanical properties are reduced, due to that those needles are prone to develop cracks, which reduce the ductility and strength of the material.
  • strontium effect is not permanent, their effect is enough to achieve rounded shapes of the eutectic structures.
  • the addition of strontium is performed by use of aluminium-strontium alloys.
  • the grains starting to rise are constituted by an ⁇ solid solution enriched with aluminium, which has a very limited capacity for containing silicon.
  • the precipitated crystalline grain contains, with regard to the initial chemical composition, very little silicon and, subsequently, when the solidification of the ⁇ phase advances the remaining liquid tends to be more and more enriched with said element, then solid and liquid will show different chemical composition.
  • the starting temperature of the solidification slightly varies depending on the silicon content, final temperature is constant and it represents the condition of maximum solubility of silicon in the ⁇ -aluminium solid solution, moreover being the minimum temperature where any aluminium-silicon alloy is at liquid state.
  • an aluminium-silicon solid solution coexists with a liquid phase referred as eutectic liquid.
  • the microstructure of Aluminium-silicon alloys is fundamentally constituted by dendrites of ⁇ -aluminium phase and eutectic cells of ⁇ -aluminium plus silicon, furthermore observing, depending on the content in other constitutive or residual elements, the presence of other phases of various tertiary eutectics which are rich in iron, in magnesium, and in copper, which are usually found as precipitates in ⁇ -aluminium intergranular regions.
  • strontium to A356 alloy with the object of modifying its structure
  • strontium cannot be indiscriminately added, the addition has to be performed inside the limits of the effective composition range for strontium in the alloy. So, for the addition of this element in the modification treatment, there exist both a minimum value, below that is not possible to obtain a suitable modification, and a maximum value, over that the effect referred as over-modification occurs, as shown in Figures 10-12 .
  • the inventors have found that suitably modifying the alloy by the addition of the appropriate proportions of silver and strontium according to the present invention, is possible to obtain round-shaped silicon particles with a very little size which precipitate in the eutectic, thus improving the mechanical properties of the alloy.
  • the chemical composition of the aluminium alloy according to the present invention consists essentially of 6.5 to 7.5 percent silicon, 0.2 to 0.4 percent magnesium, 0.1 to 0.2 percent titanium (Ti), 0.05 to 0.4 percent silver, 0.002 to 0.04 percent strontium, and the balance comprising aluminium and unavoidable impurities: ⁇ 0.15% Fe, ⁇ 0.05% Cu and ⁇ 0.10% Mn.
  • the mechanical properties are not as a result of the addition of silver only, but as an appropriate combination of suitable proportions of silver and strontium, in order to achieve a perfectly modified microstructure.
  • Specially good results are obtained when a combination of silver (preferably in an amount between 0.1 to 0.2 %) and strontium (preferably in an amount between 0.02 to 0.04 %) is present in the alloy.
  • the degassing process (b) is carried out by treating the molten alloy with dry nitrogen or dry argon.
  • the molten metal is introduced into a mould.
  • This step is known as pouring step.
  • Different pouring techniques are known in the art, gravity die casting, low pressure die casting and high pressure die casting.
  • the solidifying of the part generally leaving it to reduce the temperature, allows to taking out it from the mould without risk of breaking, marks, etc.
  • the product thus obtained, after deburring, is known as rough casting part. i.e. without any later treatment (generally thermal treatment).
  • the aluminium alloy according to the present invention In order to be used as vehicular suspension parts such as a steering knuckle and a suspension arms, the aluminium alloy according to the present invention must satisfy mechanical and technological properties such as tensile strength, yield strength, elongation percentage, corrosion resistance, and also low hot cracking.
  • T6 heat treatment is which gives best results.
  • another heat treatment known in the art such as T4, T5 heat treatments may also be suitable.
  • T6 heat treatment comprises 2 steps: homogenizing and quenching-age hardening.
  • homogenizing step what is done is to support the rough casting part to high temperature, in the range from about 500 to 600 °C, during a period of time that can be of the order of 2 to 6 hours.
  • the temperature is about 540 °C and the time 6 hours.
  • the part is quenched, i.e. is undergone to a sudden cooling.
  • the step from the homogenizing furnace to the quenching must be realized in an as short as possible period of time, since otherwise it would begin the selective precipitation. According to a preferred embodiment, this time is less than 15 seconds.
  • the quenched parts are introduced again in another treatment furnace, wherein it occurs the age-hardening step.
  • This age-hardening step is carried out at low temperature, preferably in the range of about 150 to 180 °C.
  • the age-hardening step gives the mechanical and technological properties to the casting part.
  • the casting part may be subjected to a shot-blasting step, to achieve a more bright superficial aspect.
  • the aluminium alloy thus obtained has at least 300 MPa tensile strength, at least 230 MPa yield strength, and at least 9% elongation percentage.
  • Example 1 Process of preparation of the aluminium alloy.
  • the raw materials in solid state were introduced in the furnace as pure elements and as ingots of alloys of the components.
  • Ingots of the aluminium alloy A356 (basic composition) were used.
  • the different proportions of the different components of the alloy were adjusted by adding suitable amounts of such components.
  • compositions thus obtained were: Composition A A356 alloy B Si 7% + Mg 0.3% + Ag 0,2% + Ti 0.1 % + Sr 0.02% + Al balance C Si 7% + Mg 0.3% + Ag 0,1% + Ti 0.1% + Sr 0.02 + RE 0,2% + Al balance D Si 7% + Mg 0.3% + Ag 0,1% + Ti 0.1% + Sr 0.02 + RE 0,4% + Al balance RE: Rare earth elements
  • the molten alloy contains the composition of interest, it was undergone to a degassing process, by treating the molten alloy with dry nitrogen.
  • the molten metal was introduced into a mould by gravity pouring. After the mould filling, the molten metal in the mould was leaving to reduce the temperature, and then taking it out from the mould. The product thus obtained, as rough casting part, was deburred.
  • the product as rough casting part was undergone to a T6 heat treatment. During homogenizing step, the rough casting part was heated to 540 °C, during a period of time of 6 hours. Then, the part was quenched, wherein the step from the homogenizing furnace to the quenching was carried out in less than 15 seconds.
  • the quenched parts were introduced again in another treatment furnace, to carry out the age-hardening step.
  • This age-hardening step was carried out at 160 °C.
  • composition B The aluminium alloy castings of the invention, shown an improvement of their mechanical properties, when content of Ag is above 0.1%. Best results are obtained whit Ag 0.2% (composition B).
  • Example 3 Mechanical properties of tensile bars obtained in a mould with a step-shape.
  • tensile bars were prepared using the mould with a step-shape, as shows Figure 1 .
  • tensile bars made from the aluminium alloy castings of example 1, were prepared from each area (2 per area), and the influence of thickness and improvement of results were determined. Parameters taken into account were composition and cooling speed when tests were running with and without refrigeration.
  • composition B of example 2 Aluminium alloy castings with Ag 0.2% (composition B of example 2), i.e. thin area bar (5), with external refrigeration, the mechanical properties resulted in a substantial improvement respect to A356 properties.
  • compositions C and D of example 2 shown an improvement in the mechanical properties respect to A356 properties.
  • the initial composition contains: 7.12% Si + 0.28% Mg + 0.2% Ag + 0.16% Ti, and the balance aluminium and unavoidable impurities (less than 0.12% Fe + 0.002% Cu +0.001% Mn).
  • the metalographic probes of the assay were extracted from the most unfavorable area in the piece.
  • strontium was: 50 ppm, 100 ppm, 150 ppm, 200 ppm, 300 ppm and 400 ppm.
  • Figures 13-18 show micrographs corresponding to the results obtained with each of the above additions.

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)
  • Forging (AREA)
  • Continuous Casting (AREA)

Description

  • The present invention relates to aluminium alloys. Particularly, the present invention is directed to an aluminium alloy which exhibits suitable tensile strength, yield strength and elongation percentage for its use to manufacture vehicular suspension parts.
  • BACKGROUND ART
  • Aluminium alloys are widely used as materials for various components of vehicles, industrial machines, airplanes, electric appliances for domestic use and other apparatus of various types. Among such aluminium alloys there are cast aluminium alloys, a representative of which is A356. Such cast aluminium alloys are used in important durable parts requiring higher mechanical properties such as vehicle components, metal fittings for stringing and components of hydraulic systems, and in like applications. Typical mechanical property values of the A356 alloy as treated by a T6 heat treatment (a sort of a refining treatment) are 250 MPa tensile strength, 200 MPa yield strength and 5 % elongation. The A356 alloy has widespread applications for structural components in the automotive, aerospace, and general engineering industries because of their excellent castability, corrosion resistance, and, particularly, high strength-to-weight ratio in the heat-treated condition.
  • The microstructures of alloy A356 are comprised of an aluminium matrix, which is strengthened by MgSi precipitates and, to a far lesser extent, by Si precipitates, and a dispersion of eutectic Al-Si particles and Fe-rich intermetallics. The variables affecting the microstructure mainly include composition, solidification conditions, and heat treatment.
  • The composition of A356 alloy comprises the following components: 91 to 93 wt % of Al; 6.5 to 7.5 wt % of Si; 0.20 to 0.40 wt % of Mg; 0 to 0.02 wt % of Cu; 0 to 0.20 wt % of Fe; 0 to 0.10 wt % of Mn; 0 to 0.20 wt % of Ti; and 0 to 0.10wt%ofZn.
  • Another known aluminium die casting alloys for automotive structural applications have silicon contents between about 9-11 % by weight. Examples of these alloys include C448 and Silafont 36. The high Si content of these alloys results in brittle Al-Si eutectic networks in the as-cast condition. In order to increase ductility, fracture toughness, and crushability, these alloys need a high temperature solution heat treatment that serves, principally, to break down the eutectic network and to spheroidize the Si particles. The solution heat treatment increases costs and also introduces part distortion which requires straightening or machining, which adds cost in the manufacturing process.
  • US 6364970 is directed to a hypoeutectic aluminium-silicon alloy. The alloy according to the US 6364970 patent,also known in industry as Silafont 36, contains an iron content of up to 0.15% by weight and a strontium refinement of 30 to 300 ppm (0.003 to 0.03% by weight). It has a high fracture strength resulting from the refined eutectic silicon phase and resulting from the addition of Sr to the alloy. The alloy further contains 0.5 to 0.8% by weight manganese (Mn).
  • A material used for a vehicular suspension part such as a steering knuckle and a suspension arm is required to have high tensile strength, high yield strength, sufficient elongation percentage, as well as other technological properties such as corrosion resistance, low hot cracking, etc. Accordingly, it is desirable to provide an aluminium alloy with said properties.
  • The aluminium casting alloy Anticorodal-78 dv, with a chemical composition in wt % of 6.5-7.5 % Si, up to 0.15 % Fe, up to 0.02 % Cu, up to 0.05 % Mn, 0.30-0.45 % Mg, up to 0.07 % Zn, 0.10-0.18 % Ti in addition of Sr and the balance Al, is described in "Hüttenaluminium Gusslegierungen" 1994, Aluminium Rheinfelden GMGH. The Anticorodal-78 dv alloy does not contains silver nor rare earth elements.
  • An aluminium alloy with a very similar composition to Anticorodal-78 dv is described in CN1693508 . The chemical composition consist of in wt % 6.7 % Si, 0.37 % Mg, 0.109 % Fe, 0.10 % Ti, 0.03 % Sr and balance Al.
  • EP1657319 describes AlSi7Mg and AlSi7MgCu alloys with the addition of 0.1-1.0 % Ag. The AlSi7Mg alloy herein described does not contain any strontium content. It is disclosed that the addition of silver, have no significant effect on the mechanical properties of the AlSi7Mg alloy.
  • In Vasilakos A.N. et. al. "Thermodynamic analysis and mechanical properties of cast aluminium alloy A357 with Cu, Ag and Sm additions" Metall, Huethig, Heidelberg, DE, , there are described different aluminium alloys wherein the A357 alloy is modified by the incorporation of Cu, Cu+Ag and Cu+Sm.
  • SUMMARY OF THE INVENTION
  • The problem to be solved by the present invention is to provide an aluminium alloy with improved mechanical and technological properties suitable for vehicular suspension parts. The solution is based on that the present inventors have found that an aluminium modified alloy containing silver and strontium in suitable amounts obtained by the process of the present invention, has an improved tensile strength, yield strength, and elongation percentage, and also suitable technological properties such as corrosion resistance and low hot cracking, compared to A356 aluminium alloy.
  • These characteristics of the novel alloy of the present invention make it particularly suitable for durable components requiring higher mechanical properties such as vehicle components, particularly for suspension vehicle components such as steering knuckles and suspension arms. Furthermore, the new alloy is low in cost.
  • Accordingly, an aspect of the invention relates to an aluminium alloy according to claim 1.
  • Another aspect of the invention relates to a process of making an aluminium alloy according to claim 7.
  • Another aspect of the present invention relates to the use of the aluminium alloy casting described herein, as a vehicular suspension component according to claim 11.
  • By using this aluminium alloy casting, vehicular suspension components, such as steering knuckle and a suspension arms, can be manufactured properly. Therefore, another aspect of the invention provides a vehicular suspension component according to claim 13 which is made from an aluminium alloy casting as described herein.
  • DETAILED DESCRIPTION OF THE INVENTION:
  • As it is said above, by adding the appropriate amounts of silver (Ag) and strontium (Sr) described herein to the basic composition and the method of the present invention, an improvement of the tensile strength, yield strength, and elongation percentage, suitable technological properties such as corrosion resistance and low hot cracking, of the A356 aluminium alloy (basic composition) is observed.
  • By the addition of the appropriate amounts of Ag and Sr to the aluminium alloy of the above basic composition, the precipitation hardening elements included in the alloy, magnesium (Mg) and silicon (Si), are more finely dispersed in the alloy and precipitate. Thus an improvement of the above mentioned mechanical and technological properties of the aluminium alloy casting by the fine precipitation of these precipitates are obtained.
  • Preferably, the chemical composition for the aluminium alloy according to the present invention consists essentially 6.5 to 7.5 percent silicon, 0.2 to 0.4 percent magnesium, 0.1 to 0.2 percent titanium (Ti), 0.05 to 0.3 percent silver, 0.002 to 0.04 percent strontium, and the balance comprising aluminium and unavoidable impurities. According to an embodiment of the invention, the aluminium alloy contains between 0.02 to 0.04 percent strontium and between 0.1 to 0.25 percent silver. More preferably, more than 0.02 percent strontium up to 0.04 percent, and between 0.1 to 0.2 percent silver.
  • Particularly preferred, are aluminium alloys wherein the content of strontium is 0.025, 0.03, 0.032, 0.035 or 0.04 percent.
  • According to an embodiment of the invention, the aluminium alloy contains, by percentage of weight, 0.2 percent silver.
  • Ag is an essential element of the aluminium alloys of the present invention, due to its contribution to the increased fineness of the eutectic Si structure, the increased fineness of the needle iron (Fe) structure, and the increased uniformity and fineness of the precipitation hardening alloys of Mg, and Si which is suitable for improve the properties above mentioned. In the present invention, the Ag content is at least 0.05 wt %.
  • Ti is an element added for making the grains of the casting finer to improve the mechanical properties and mainly the ductility of the part. In the present invention, the Ti content is defined as within a range from 0.1 to 0.2 wt %.
  • Mg is an essential hardening agent developed after heat treatment in Al-Si alloys. The hardening phase Mg2Si is limited by solubility, which corresponds approximately until 0.7 % wherein maximum hardness is reached. In the present invention, the Mg content is defined as within a range from 0.2 to 0.4 wt %.
  • Si is an essential element depositing together with Mg as Mg2Si by artificial aging to provide high strength (yield strength) for final products upon use. Its addition improves the flowability (castability), the hot strength, and other properties of the alloy. Alloys with less than 12% of Si are referred to as hypoeutectic, those with close to 12% Si as eutectic, and those with over 12% Si as hypereutectic. Modification of hypoeutectic alloys (<12% Si) is particularly advantageous in sand castings and can be effectively achieved through the addition of a controlled amount of sodium or strontium, which refines the eutectic phase. In general, the optimum range of Si depends on the process, e.g. in sand castings amounts between 5 to 7 wt % , in die casting amounts between 7 to 9 wt %, in high pressure die casting between 8 to 12 wt %. The addition of Si not only improves the mechanical properties, but also reduces the density and thermal expansion rate. In the present invention, the Si content, is defined as within the range from 6.5 to 7.5 wt %.
  • Sr modification of aluminium alloys, reduces the size and aspect ratio of the eutectic silicon particles. In comparison with the unmodified alloys, the strontium modified alloys show higher ductility, particularly the A356 alloy, but slightly lower yield strength.
  • According to an embodiment of the present invention the aluminium alloy further comprises, by percentage of weight, 0.1 to 0.6 % of rare earth elements. More preferably, the aluminium alloy contains, by percentage of weight, 0.4 % of rare earth elements. Preferably, said rare earth element is at least one element selected from the group comprising La, Ce, Pr, Nb, Pm, Sm, Eu, Ga, Tb, Dy, Ho, Er, Tm, Yb, Lu, Y, and Sc. More preferred are those selected from the group consisting of La, Ce, Pr and Nd. Generally, rare earth elements are eliminated as slag in refusions.
  • According to a preferred embodiment, the aluminium alloy contains, by percentage of weight, between 0.05 and 0.2 percent silver and between 0.2 and 0.5 percent of rare earth elements. More preferably, between 0.1 and 0.2 percent silver and between 0.3 and 0.4 percent of rare earth elements. Particularly preferred are those wherein the content of silver is 0.1 percent and the content of rare earth elements is 0.4 percent.
  • By adding slight amounts of rare earth elements the casting defects of the aluminium alloy casting are reduced, increased uniformity of structure and increased fineness of dispersion are achieved, and the strength of the aluminium alloy casting is strikingly improved. Furthermore, presence of rare earth elements contributes to make the grain size of the casting finer improving its strength and ductility, and modifies the eutectic structure of Al-Si alloys. Another advantage of the presence of rare earth elements in the aluminium alloys of the present invention is that it reduces the costs, due to it permits to reduce the amount of Ag in the composition.
  • Preferably, the alloys according to the present invention are substantially free of copper and iron. The term "substantially free" means having no significant amount of that component purposely added to the alloy composition, it being understood that trace amounts of unavoidable impurities may find their way into a desired end product.
  • Copper substantially improves strength and hardness in the as-cast and heat-treated conditions. Alloys containing 4 to 6% Cu respond most strongly to thermal treatment. Copper generally reduces resistance to general corrosion and, in specific compositions and material conditions, stress corrosion susceptibility. Additions of copper also reduce hot tear resistance and decrease castability.
  • Iron improves hot tear resistance and decreases the tendency for die sticking or soldering in die casting. Increases in iron content are, however, accompanied by substantially decreased ductility. Iron reacts to form a myriad of insoluble phases in aluminium alloy melts, the most common of which are FeAl3, FeMnAl6 and α-AlFeSi. These essentially insoluble phases are responsible for decrease in mechanical properties, such as elongation and tensile strength, especially at elevated temperature. As the fraction of insoluble phase increases with increased iron content, casting considerations as flowability and feeding characteristics are adversely affected. Iron participates in the formation of sludging phases with manganese, chromium and other elements.
  • Therefore, the aluminium alloy of the present invention is substantially free of copper and iron, i.e. it has no significant amount of those components purposely added to the alloy composition, nevertheless it is understood that trace amounts of unavoidable impurities may find their way into a desired end product. Preferably, the content of iron in the aluminium alloys of the present invention is lower than 0.15 % wt.
  • The aluminium alloy described herein can be prepared by a process comprising (a) melting the raw materials, alloying elements and auxiliary materials in suitable amounts to obtain the composition and properties of interest; (b) undergone the molten alloy thus obtained to a degassing process, and (c) introducing (pouring) the molten metal in a mould and reduce the temperature until solidifying as rough casting parts.
  • Preferably, the raw materials in solid state are introduced in the furnace as pure elements or as alloys of the components. Generally, ingots of the aluminium alloy A356 (basic composition) are introduced into the furnace, then alloying elements are added, and then when the ingots are melt, the composition of the molten metal is analyzed and optionally, if necessary, the proportions of the components in the alloy are adjusted by adding suitable amounts of such components or alternatively diluted the molten by adding aluminium ingots and then adding suitable amounts of the components to adjust their proportion. Once the molten metal contains the desired composition, additives are added in order to achieve the suitable mechanical and technological properties. Such additives are the modifying agent strontium and the refining agent titanium.
  • The modifying agent, is used in order to achieve that the eutectic structure aluminium-silicon, which precipitates during the solidifying step of the part, shows a rounded shape, instead of a needle shape characteristic wherein no modifying is present. When the eutectic structure shows a needle shape, the mechanical properties are reduced, due to that those needles are prone to develop cracks, which reduce the ductility and strength of the material.
  • In spite of that some experts thinks that strontium effect is not permanent, their effect is enough to achieve rounded shapes of the eutectic structures. Preferably, the addition of strontium is performed by use of aluminium-strontium alloys.
  • During the solidification of an aluminium-silicon alloy, the chemical composition of the liquid metal, over which the solid phases precipitate, does not remain constant in time, but it is constantly varying, seriously affecting both the evolution of the solidification and the rise of the various phases.
  • For example, in the case of an aluminium alloy with a silicon content below 12.6% (hypoeutectic), the grains starting to rise are constituted by an α solid solution enriched with aluminium, which has a very limited capacity for containing silicon. Thus, the precipitated crystalline grain contains, with regard to the initial chemical composition, very little silicon and, subsequently, when the solidification of the α phase advances the remaining liquid tends to be more and more enriched with said element, then solid and liquid will show different chemical composition. The starting temperature of the solidification slightly varies depending on the silicon content, final temperature is constant and it represents the condition of maximum solubility of silicon in the α-aluminium solid solution, moreover being the minimum temperature where any aluminium-silicon alloy is at liquid state. At the final temperature of the solidification, an aluminium-silicon solid solution coexists with a liquid phase referred as eutectic liquid.
  • When said liquid is sub-cooled, it solidifies precipitating at once the aluminium-silicon solid solution and pure silicon grains. This solid solution, intimately linked to silicon grains, is referred as eutectic α phase, and it is different from primary α phase, with dendritic morphology.
  • According to the above disclosure, as conclusion the microstructure of Aluminium-silicon alloys is fundamentally constituted by dendrites of α-aluminium phase and eutectic cells of α-aluminium plus silicon, furthermore observing, depending on the content in other constitutive or residual elements, the presence of other phases of various tertiary eutectics which are rich in iron, in magnesium, and in copper, which are usually found as precipitates in α-aluminium intergranular regions.
  • The addition of strontium to A356 alloy with the object of modifying its structure is already well-known, however strontium cannot be indiscriminately added, the addition has to be performed inside the limits of the effective composition range for strontium in the alloy. So, for the addition of this element in the modification treatment, there exist both a minimum value, below that is not possible to obtain a suitable modification, and a maximum value, over that the effect referred as over-modification occurs, as shown in Figures 10-12.
  • In the case of components made of A356 alloy and subjected to heat treatment for solution, both the aluminium alloy suppliers and the general literature recommend for the modification treatment an strontium addition range comprised between 50 and 150 ppm (from 0.0050% to 0.0150% in weight of the alloy composition).
  • The inventors have found that suitably modifying the alloy by the addition of the appropriate proportions of silver and strontium according to the present invention, is possible to obtain round-shaped silicon particles with a very little size which precipitate in the eutectic, thus improving the mechanical properties of the alloy.
  • As defined above the chemical composition of the aluminium alloy according to the present invention consists essentially of 6.5 to 7.5 percent silicon, 0.2 to 0.4 percent magnesium, 0.1 to 0.2 percent titanium (Ti), 0.05 to 0.4 percent silver, 0.002 to 0.04 percent strontium, and the balance comprising aluminium and unavoidable impurities: < 0.15% Fe, < 0.05% Cu and < 0.10% Mn.
  • Accordingly, in the alloy of the invention, the mechanical properties are not as a result of the addition of silver only, but as an appropriate combination of suitable proportions of silver and strontium, in order to achieve a perfectly modified microstructure. Specially good results are obtained when a combination of silver (preferably in an amount between 0.1 to 0.2 %) and strontium (preferably in an amount between 0.02 to 0.04 %) is present in the alloy.
  • This fact is demonstrated when testing the results of the improvement of the mechanical properties of the alloy of the invention, with regard to those observed in the state of the art. Thus, for example, in the European patent application EP 1657319 , wherein an aluminium AlSi7Mg alloy is described, the addition of 0.5 % silver scarcely improve the yield strength and tensile strength of the alloy (see Figure 1, alloys 3 and 4).
  • During melting step, due to the humidity of materials and ambient, and as a result of the avidity of the aluminium for the oxygen, Al2O3 (alumina) and H2 are formed. The alumina formed happens to form part of the slag and free hydrogen that is generated dissolves in the molten metal. The presence of hydrogen in the solidified part, is the responsible of the presence of pores, which reduces the ductility and tensile strength. Then once the molten alloy contains the composition of interest, it is undergone to a degassing process, which does not modify neither its chemical composition, nor its metallurgical properties.
  • According to an embodiment of the invention, the degassing process (b) is carried out by treating the molten alloy with dry nitrogen or dry argon.
  • After degassing step, the molten metal is introduced into a mould. This step is known as pouring step. Different pouring techniques are known in the art, gravity die casting, low pressure die casting and high pressure die casting. After the mould filling, the solidifying of the part, generally leaving it to reduce the temperature, allows to taking out it from the mould without risk of breaking, marks, etc. The product thus obtained, after deburring, is known as rough casting part. i.e. without any later treatment (generally thermal treatment).
  • In order to be used as vehicular suspension parts such as a steering knuckle and a suspension arms, the aluminium alloy according to the present invention must satisfy mechanical and technological properties such as tensile strength, yield strength, elongation percentage, corrosion resistance, and also low hot cracking.
  • To improve the mechanical and technological properties of the alloy, it is submitted to a heat treatment. Different heat treatment are known, nevertheless due to the high requirements of mechanical and technological properties for durable components such as vehicle components, particularly for suspension vehicle components such as a steering knuckles and suspension arms, T6 heat treatment is which gives best results. Anyhow, another heat treatment known in the art (such as T4, T5 heat treatments) may also be suitable.
  • T6 heat treatment comprises 2 steps: homogenizing and quenching-age hardening. During homogenizing step, what is done is to support the rough casting part to high temperature, in the range from about 500 to 600 °C, during a period of time that can be of the order of 2 to 6 hours. Preferably the temperature is about 540 °C and the time 6 hours.
  • Once the microstructure is homogenized, the part is quenched, i.e. is undergone to a sudden cooling. The step from the homogenizing furnace to the quenching must be realized in an as short as possible period of time, since otherwise it would begin the selective precipitation. According to a preferred embodiment, this time is less than 15 seconds.
  • Next, the quenched parts are introduced again in another treatment furnace, wherein it occurs the age-hardening step. This age-hardening step is carried out at low temperature, preferably in the range of about 150 to 180 °C. The age-hardening step gives the mechanical and technological properties to the casting part.
  • The casting part may be subjected to a shot-blasting step, to achieve a more bright superficial aspect.
  • The aluminium alloy thus obtained, has at least 300 MPa tensile strength, at least 230 MPa yield strength, and at least 9% elongation percentage.
  • Additional objects, advantages and features of the invention will become apparent to those skilled in the art upon examination of the description or may be learned by practice of the invention. The following examples and drawings are provided by way of illustration, and are not intended to be limiting of the present invention.
  • BRIEF DESCRIPTION OF THE DRAWINGS
    • Figure 1. Tensile bar obtained from the step-shape mould
    • Figure 1A. Graphical representation of the tensile bars obtained from the different areas of the step-shape mould (1-6).
    • Figure 1 B. Wall thickness of the different areas (mm)
    • Figure 2. Tensile strength (TS) and yield strength (YS) of tensile bar samples from thin area 5 made with external refrigeration.
      Graphical representation of tensile strength (TS) and yield strength (YS) of the tensile bars, made from the aluminium alloy castings of example 1, prepared from thin area 5 with external refrigeration, and standard A356 alloy bar.
    • Figure 3. % Elongation (% E) of tensile bar samples from thin area 5 made with external refrigeration.
      Graphical representation of elongation (E) of the tensile bars, made from the aluminium alloy castings of example 1, prepared from thin area 5 with external, refrigeration, and standard A356 alloy bar.
    • Figure 4. Tensile strength (TS) and yield strength (YS) of tensile bar samples from thin area 5 made without external refrigeration.
      Graphical representation of tensile strength (TS) and yield strength (YS) of the tensile bars, made from the aluminium alloy castings of example 1, prepared from thin area 5 without external refrigeration, and standard A356 alloy bar.
    • Figure 5. % Elongation (% E) of tensile bar samples from thin area 5 made without external refrigeration.
      Graphical representation of elongation (E) of the tensile bars, made from the aluminium alloy castings of example 1, prepared from thin area 5 without external refrigeration, and standard A356 alloy bar.
    • Figure 6. Tensile strength (TS) and yield strength (YS) of tensile bar samples from thick area 3 made with external refrigeration.
      Graphical representation of tensile strength (TS) and yield strength (YS) of the tensile bars, made from the aluminium alloy castings of example 1, prepared from thick area 3 with external refrigeration, and standard A356 alloy bar.
    • Figure 7. % Elongation (% E) of tensile bar samples from thick area 3 made with external refrigeration.
      Graphical representation of elongation (E) of the tensile bars, made from the aluminium alloy castings of example 1, prepared from thick area 3 with external refrigeration, and standard A356 alloy bar.
    • Figure 8. Tensile strength (TS) and yield strength (YS) of tensile bar samples from thick area 3 made without external refrigeration.
      Graphical representation of tensile strength (TS) and yield strength (YS) of the tensile bars, made from the aluminium alloy castings of example 1, prepared from thick area 3 without external refrigeration, and standard A356 alloy bar.
    • Figure 9. % Elongation (% E) of tensile bar samples from thick area 3 made without external refrigeration.
      Graphical representation of elongation (E) of the tensile bars, made from the aluminium alloy castings of example 1, prepared from thick area 3 without external refrigeration, and standard A356 alloy bar.
    • Figure 10. A356 alloy microstructure, without modification.
      This figure shows the microstructure of A356 alloy without modification, wherein silicon crystals have needle shape.
    • Figure 11. A356 alloy microstructure suitably modified.
      This figure shows the microstructure of A356 alloy suitably modified.
    • Figure 12. A356 alloy microstructure overmodified.
      This figure shows the microstructure of A356 alloy overmodified wherein silicon crystals, instead of rounded, will show a more coarse structure in the α-aluminium dendrites borders, impairing the mechanical properties of the part.
    • Figures 13-18. Show the microstrutructure of the alloy of the invention modified by the addition of various amounts of Sr from 50 ppm to 400 ppm.
    DETAILED DESCRIPTION OF PARTICULAR EMBODIMENTS Example 1. Process of preparation of the aluminium alloy.
  • The raw materials in solid state were introduced in the furnace as pure elements and as ingots of alloys of the components. Ingots of the aluminium alloy A356 (basic composition) were used. And the different proportions of the different components of the alloy were adjusted by adding suitable amounts of such components.
  • The compositions thus obtained were:
    Composition
    A A356 alloy
    B Si
    7% + Mg 0.3% + Ag 0,2% + Ti 0.1 % + Sr 0.02% + Al balance
    C Si
    7% + Mg 0.3% + Ag 0,1% + Ti 0.1% + Sr 0.02 + RE 0,2% + Al balance
    D Si
    7% + Mg 0.3% + Ag 0,1% + Ti 0.1% + Sr 0.02 + RE 0,4% + Al balance
    RE: Rare earth elements
  • Once the molten alloy contains the composition of interest, it was undergone to a degassing process, by treating the molten alloy with dry nitrogen.
  • After degassing step, the molten metal was introduced into a mould by gravity pouring. After the mould filling, the molten metal in the mould was leaving to reduce the temperature, and then taking it out from the mould. The product thus obtained, as rough casting part, was deburred.
  • The product as rough casting part was undergone to a T6 heat treatment. During homogenizing step, the rough casting part was heated to 540 °C, during a period of time of 6 hours. Then, the part was quenched, wherein the step from the homogenizing furnace to the quenching was carried out in less than 15 seconds.
  • Next, the quenched parts were introduced again in another treatment furnace, to carry out the age-hardening step. This age-hardening step was carried out at 160 °C.
  • Example 2. Mechanical properties.
  • To test the mechanical properties of the aluminium alloy casting in accordance with the present invention, a number of tensile bar samples with different content of Ag and rare earth elements, were prepared and subjected to testing, and compared with A356 alloy.
  • Tensile strength, yield strength and elongation were measured. The results of the tests, and the compositions of each of the tested alloy castings are set forth in Table 1. Table 1. Mechanical properties of tested alloy castings.
    Composition Refrigeration Area 3 Area 5
    Tensile strength (MPa) Yield strength (MPa) Elongation strength (%) Tensile strength (MPa) Yield strength (MPa) Elongation (%)
    (A) A-356 alloy Yes 256 196 4,8 272 201 6,2
    No 243 187 4,2 264 199 5,6
    (B) Si 7% + Mg 0.3% + Ag 0,2% + Ti0.1% + Sr 0.02% + Al balance Yes 285 219 7,5 305 234 10,6
    No 278 213 6,6 292 226 9,6
    (C) Si 7% + Mg 0.3% + Ag 0,1% + Ti 0.1% + Sr 0.02 + RE 0,2% + Al balance Yes 277 209 5,7 292 221 7,5
    No 265 197 4,8 286 222 8
    (D) Si 7% + Mg 0.3% + Ag 0,1% + Ti0.1%+Sr0.02+ RE 0,4% + Al balance Yes 282 208 6,3 296 215 8,4
    No 273 202 5,1 292 210 6,8
  • The aluminium alloy castings of the invention, shown an improvement of their mechanical properties, when content of Ag is above 0.1%. Best results are obtained whit Ag 0.2% (composition B).
  • Example 3. Mechanical properties of tensile bars obtained in a mould with a step-shape.
  • Different tensile bars were prepared using the mould with a step-shape, as shows Figure 1. Thus, tensile bars, made from the aluminium alloy castings of example 1, were prepared from each area (2 per area), and the influence of thickness and improvement of results were determined. Parameters taken into account were composition and cooling speed when tests were running with and without refrigeration.
  • The results of the tests, with and without refrigeration, of tested tensile bars from areas 5 (thin area) and 3 (thick area) are set forth in Figures 2 to 9.
  • Aluminium alloy castings with Ag 0.2% (composition B of example 2), i.e. thin area bar (5), with external refrigeration, the mechanical properties resulted in a substantial improvement respect to A356 properties.
  • Bars prepared with Ag 0.1 % and RE 0.2% and RE 0.4 % (compositions C and D of example 2), shown an improvement in the mechanical properties respect to A356 properties.
  • Example 4. Effect of the strontium addition.
  • When the contents on the rest of the constitutive elements of the alloy remain constant, and only the content on strontium is varied, the combined effect of said element could be determined along with that of the addition of silver.
  • Different alloys were prepared with compositions corresponding to that proposed by the invention, wherein 0.2% in weight of silver was added and the amounts of added strontium were varied. Thus, the initial composition contains: 7.12% Si + 0.28% Mg + 0.2% Ag + 0.16% Ti, and the balance aluminium and unavoidable impurities (less than 0.12% Fe + 0.002% Cu +0.001% Mn).
  • In order to determine the effectiveness of the modification, the metalographic probes of the assay were extracted from the most unfavorable area in the piece.
  • The added amounts of strontium were: 50 ppm, 100 ppm, 150 ppm, 200 ppm, 300 ppm and 400 ppm.
  • Figures 13-18 show micrographs corresponding to the results obtained with each of the above additions.
  • With 50 ppm of strontium, acicular structures and globulized crystals coexist in the structure of the silicon. With 100 ppm of strontium, both morphologies of the silicon crystals coexist in quite the same proportion. With 150 ppm of strontium, silicon structure is essentially formed by globulized crystals. With 200 ppm, 300 ppm and 400 ppm of strontium, the only silicon morphology in the structure is.formed by globulized crystals, not detecting the presence of silicon sheets.
  • Thus, on the basis of the above results, it is concluded that, in the alloy of the invention, a modification of the alloy microstructure is achieved with the presence of 0.2% of silver and above strontium levels (of 50 to 400 ppm), improving the mechanical properties thereof. The improvement of the microstructure is greater when adding between 200 ppm and 400 ppm of strontium.
  • Example 5. Effect of the silver addition.
  • The mechanical properties of an aluminium alloy casting with the following composition: 7.12% Si + 0.28% Mg + 0.2% Ag + 0.02% Sr + 0.16% Ti, and the balance aluminium and unavoidable impurities (less than 0.12% Fe + 0.002% Cu + 0.001% Mn) were subjected to testing.
  • Tensile strength, yield strength and elongation were measured. The results of the tests were the following:
    • Tensile strength: 322 MPa
    • Yield strength: 259 MPa
    • Elongation: 13.5%

Claims (14)

  1. An aluminium alloy consisting of, by percentage of weight:
    6.5 to 7.5 percent silicon;
    0.2 to 0.4 percent magnesium;
    0.1 to 0.2 percent titanium;
    0. 05 to 0.3 percent silver;
    0.002 to 0.04 percent strontium;
    optionally 0.1 to 0.6 %, by percentage of weight, of rare earth elements;
    and the balance aluminium and unavoidable impurities.
  2. The aluminium alloy of claim 1, which contains, by percentage of weight, between 0.1 to 0.2 percent silver.
  3. The aluminium alloy according to any of claims 1 to 2, which contains, by percentage of weight, 0.1 percent silver and 0.4 percent of rare earth elements.
  4. The aluminium alloy according to claim 3, wherein said rare earth element is at least one element selected from the group consisting of La, Ce, Pr, Nb, Pm, Sm, Eu, Ga, Tb, Dy, Ho, Er, Tm, Yb, Lu, Y, and Sc.
  5. The aluminium alloy according to any of claims 1 to 4, which contains, by percentage of weight, more than 0.02 up to 0.04 percent strontium.
  6. The aluminium alloy according to any of claims 1 to 5, which contains, by percentage of weight, between 0.025 to 0.04 percent strontium and between 0.1 to 0.2 percent silver.
  7. A process for the preparation of the aluminium alloy of any of claims 1 to 6, comprising (a) melting the raw materials, alloying elements and auxiliary materials in suitable amounts to obtain the composition and properties of interest; (b) undergone the molten alloy thus obtained to a degassing process, and (c) introducing the molten metal in a mould and reduce the temperature until solidifying as rough casting parts.
  8. The process according to claim 7, wherein the degassing process is carried out by treating the molten alloy with dry nitrogen or dry argon.
  9. The process according to any of claims 7 and 8, wherein the raw materials are introduced in the furnace as pure elements or as alloys of the elements.
  10. The process according to any of claims 7 to 9, wherein the proportions of the components in the alloy are adjusted by
    a) adding suitable amounts of such components; or alternatively
    b) diluting the molten metal resulting of melting pure alloying elements and/or alloys of the components, by adding aluminium ingots and then adding suitable amounts of the components to adjust their proportion.
  11. Use of the aluminium alloy as defined in any of the claims 1 to 6, for making a cast vehicular suspension component.
  12. Use of the aluminium alloy according to claim 11, wherein the vehicular suspension component is selected from steering knuckle and suspension arms.
  13. A vehicular suspension component cast from the aluminium alloy as defined in any of claims 1 to 6.
  14. The vehicular suspension component of claim 13 which is selected from steering knuckle and suspension arms.
EP07014135.3A 2006-07-27 2007-07-19 Aluminium alloy Not-in-force EP1882754B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP07014135.3A EP1882754B1 (en) 2006-07-27 2007-07-19 Aluminium alloy

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP06015671A EP1882753A1 (en) 2006-07-27 2006-07-27 Aluminium alloy
EP07014135.3A EP1882754B1 (en) 2006-07-27 2007-07-19 Aluminium alloy

Publications (2)

Publication Number Publication Date
EP1882754A1 EP1882754A1 (en) 2008-01-30
EP1882754B1 true EP1882754B1 (en) 2016-07-13

Family

ID=38872137

Family Applications (1)

Application Number Title Priority Date Filing Date
EP07014135.3A Not-in-force EP1882754B1 (en) 2006-07-27 2007-07-19 Aluminium alloy

Country Status (1)

Country Link
EP (1) EP1882754B1 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110527873A (en) * 2019-09-29 2019-12-03 合肥工业大学 A kind of chassis auxiliary frame Al-Si-Mg-Ti-N-Sc alloy and preparation method thereof

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102312137B (en) * 2011-09-09 2016-06-22 深圳市中兴康讯电子有限公司 Aluminum-silicon-magnesium Cast aluminium alloy gold and casting technique
AT14019U1 (en) * 2014-02-14 2015-02-15 Amag Casting Gmbh cast alloy
CN105441729A (en) * 2015-12-03 2016-03-30 黄波 High-conductivity anti-stretching aluminum alloy conductor and preparation method thereof
CN105506397A (en) * 2015-12-03 2016-04-20 黄波 Corrosion-resistant aluminum alloy conductor containing promethium element and preparation method of corrosion-resistant aluminum alloy conductor
CN109136696B (en) * 2018-08-08 2023-11-03 倧奇健康科技有限公司 Infrared radiation material, preparation method thereof and infrared emission base material
CN111455231A (en) * 2020-04-21 2020-07-28 昆明冶金研究院有限公司 Composite rare earth RE cast aluminum alloy material and preparation method thereof
CN115198150B (en) * 2022-06-24 2023-10-13 一汽解放汽车有限公司 Aluminium-silicon alloy and its preparation method and application
CN115261685B (en) * 2022-08-10 2023-05-26 中南大学 Cast aluminum-silicon-magnesium alloy for automobile and preparation method thereof
CN117604341A (en) * 2024-01-23 2024-02-27 中信戴卡股份有限公司 High impact toughness aluminium magnesium silicon alloy material and casting method of component

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CH689143A5 (en) 1994-06-16 1998-10-30 Rheinfelden Aluminium Gmbh Aluminum-silicon casting alloys with high corrosion resistance, particularly for safety components.
AU3813795A (en) * 1994-09-26 1996-04-19 Ashurst Technology Corporation (Ireland) Limited High strength aluminum casting alloys for structural applications
US7666353B2 (en) * 2003-05-02 2010-02-23 Brunswick Corp Aluminum-silicon alloy having reduced microporosity
DE102004053746A1 (en) 2004-11-06 2006-05-11 Bayerische Motoren Werke Ag Aluminum casting alloy, useful for sand or chill casting, e.g. of automobile engine components, based on aluminum, silicon and magnesium and containing added silver to increase yield point
CN100476000C (en) 2005-05-17 2009-04-08 郑州大学 Aluminium alloy model fine crystal aluminium ingot for wheel hub and manufacturing method thereof

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110527873A (en) * 2019-09-29 2019-12-03 合肥工业大学 A kind of chassis auxiliary frame Al-Si-Mg-Ti-N-Sc alloy and preparation method thereof
CN110527873B (en) * 2019-09-29 2021-06-08 合肥工业大学 Al-Si-Mg-Ti-N-Sc alloy for chassis subframe and preparation method thereof

Also Published As

Publication number Publication date
EP1882754A1 (en) 2008-01-30

Similar Documents

Publication Publication Date Title
EP1882754B1 (en) Aluminium alloy
EP1882753A1 (en) Aluminium alloy
AU2005269483B2 (en) An Al-Si-Mg-Zn-Cu alloy for aerospace and automotive castings
EP2471967B1 (en) Method for obtaining improved mechanical properties in recycled aluminium castings free of platelet-shaped beta-phases
US20100288401A1 (en) Aluminum casting alloy
US7625454B2 (en) Al-Si-Mg-Zn-Cu alloy for aerospace and automotive castings
CN102796925B (en) High-strength die-casting aluminum alloy for pressure casting
KR101205169B1 (en) Aluminium alloy
US9322086B2 (en) Aluminum pressure casting alloy
US20180127859A1 (en) Increasing strength of an aluminum alloy
WO2005075692A1 (en) Aluminum alloy for producing high performance shaped castings
JP2010018875A (en) High strength aluminum alloy, method for producing high strength aluminum alloy casting, and method for producing high strength aluminum alloy member
WO2013144343A1 (en) Alloy and method of production thereof
US20050238529A1 (en) Heat treatable Al-Zn-Mg alloy for aerospace and automotive castings
JP3921314B2 (en) Aluminum alloy cast material excellent in impact fracture strength and method for producing the same
JP4145242B2 (en) Aluminum alloy for casting, casting made of aluminum alloy and method for producing casting made of aluminum alloy
JP4994734B2 (en) Aluminum alloy for casting and cast aluminum alloy
CN114457266A (en) Ultrahigh-strength and toughness cast aluminum alloy and forming method thereof
US20020155023A1 (en) Foundry alloy
EP1260600B1 (en) Aluminum alloy sheet material and method for producing the same
JP2003155535A (en) Aluminum alloy extruded material for automobile bracket, and production method therefor
CN115896558A (en) 4xxx series aluminum alloy forging and preparation method thereof
JP2011162883A (en) High-strength aluminum alloy, method of manufacturing high-strength aluminum alloy casting, and method of manufacturing high-strength aluminum alloy member
JPH0375329A (en) Aluminum alloy and method for its casting
JP2006316341A (en) Castable aluminum alloy and aluminum alloy cast made therefrom

Legal Events

Date Code Title Description
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

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

AX Request for extension of the european patent

Extension state: AL BA HR MK YU

17P Request for examination filed

Effective date: 20080620

17Q First examination report despatched

Effective date: 20080725

AKX Designation fees paid

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK TR

GRAP Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOSNIGR1

INTG Intention to grant announced

Effective date: 20160218

GRAS Grant fee paid

Free format text: ORIGINAL CODE: EPIDOSNIGR3

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IS IT LI LT LU LV MC MT NL PL PT RO SE SI SK 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: AT

Ref legal event code: REF

Ref document number: 812399

Country of ref document: AT

Kind code of ref document: T

Effective date: 20160715

Ref country code: CH

Ref legal event code: EP

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: 602007046955

Country of ref document: DE

REG Reference to a national code

Ref country code: LT

Ref legal event code: MG4D

REG Reference to a national code

Ref country code: NL

Ref legal event code: MP

Effective date: 20160713

REG Reference to a national code

Ref country code: AT

Ref legal event code: MK05

Ref document number: 812399

Country of ref document: AT

Kind code of ref document: T

Effective date: 20160713

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: 20160731

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

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: 20160713

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: 20161113

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: 20160713

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: 20160713

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: 20160713

REG Reference to a national code

Ref country code: DE

Ref legal event code: R119

Ref document number: 602007046955

Country of ref document: DE

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: 20160713

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: 20160713

Ref country code: ES

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: 20160713

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: 20160713

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: 20161114

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: 20160713

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: 20160713

REG Reference to a national code

Ref country code: CH

Ref legal event code: PL

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

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: 20160713

Ref country code: CH

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

Effective date: 20160731

Ref country code: LI

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

Effective date: 20160731

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: 20160713

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: 20160713

Ref country code: DE

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

Effective date: 20170201

REG Reference to a national code

Ref country code: IE

Ref legal event code: MM4A

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

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

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

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

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: 20161013

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: 20160713

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: 20160713

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: 20160713

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

Effective date: 20170428

26N No opposition filed

Effective date: 20170418

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

Effective date: 20161013

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

Ref country code: IE

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

Effective date: 20160719

Ref country code: GB

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

Effective date: 20161013

Ref country code: FR

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

Effective date: 20160913

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 NON-PAYMENT OF DUE FEES

Effective date: 20160719

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: 20160713

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

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: 20070719

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: 20160713

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

Ref country code: MT

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

Effective date: 20160731

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: 20160713

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: 20160713