EP4043602A1 - Aluminum alloy material - Google Patents

Aluminum alloy material Download PDF

Info

Publication number
EP4043602A1
EP4043602A1 EP20874847.5A EP20874847A EP4043602A1 EP 4043602 A1 EP4043602 A1 EP 4043602A1 EP 20874847 A EP20874847 A EP 20874847A EP 4043602 A1 EP4043602 A1 EP 4043602A1
Authority
EP
European Patent Office
Prior art keywords
aluminum alloy
alloy material
less
strength
orientation density
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.)
Pending
Application number
EP20874847.5A
Other languages
German (de)
French (fr)
Other versions
EP4043602A4 (en
Inventor
Tomohito KUROSAKI
Tadashi Minoda
Mitsuhiro Tamaki
Jin-Gyo Kim
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.)
UACJ Corp
Original Assignee
UACJ Corp
Glolnix Co Ltd
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
Application filed by UACJ Corp, Glolnix Co Ltd filed Critical UACJ Corp
Publication of EP4043602A1 publication Critical patent/EP4043602A1/en
Publication of EP4043602A4 publication Critical patent/EP4043602A4/en
Pending legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/06Alloys based on aluminium with magnesium as the next major constituent
    • C22C21/08Alloys based on aluminium with magnesium as the next major constituent with silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C21/00Alloys based on aluminium
    • C22C21/06Alloys based on aluminium with magnesium as the next major constituent
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21BROLLING OF METAL
    • B21B3/00Rolling materials of special alloys so far as the composition of the alloy requires or permits special rolling methods or sequences ; Rolling of aluminium, copper, zinc or other non-ferrous metals
    • 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
    • C22F1/047Changing 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 magnesium as the next major constituent
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B21MECHANICAL METAL-WORKING WITHOUT ESSENTIALLY REMOVING MATERIAL; PUNCHING METAL
    • B21BROLLING OF METAL
    • B21B3/00Rolling materials of special alloys so far as the composition of the alloy requires or permits special rolling methods or sequences ; Rolling of aluminium, copper, zinc or other non-ferrous metals
    • B21B2003/001Aluminium or its alloys

Definitions

  • the present invention relates to a high-strength aluminum alloy material having reduced strength anisotropy.
  • Typical high-strength aluminum alloys include, for example, a 6000 series alloy and a 7000 series alloy.
  • the above-described alloys are heat-treatable alloys, which require solution treatment and aging heat treatment, and thus have a problem of low production efficiency.
  • the 7000 series alloy contains Zn and Cu in a large amount, and thus have a problem of causing corrosion to easily occur depending on usage environments.
  • non-heat-treatable aluminum alloys are used in some cases.
  • Typical non-heat-treatable aluminum alloys include a 5000 series alloy, which has the highest strength.
  • the 5000 series alloy which typically has excellent corrosion resistance, does not require the solution treatment and the aging heat treatment, so that the 5000 series alloy is produced with high efficiency.
  • increase in the amount of an element added to the 5000 series alloy makes it possible to achieve the 5000 series alloy having strength not less than that of a 6000 series alloy.
  • a 5000 series aluminum alloy material containing not less than 5% by weight of Mg, which is a major additive element (see Patent Literatures 1 to 3).
  • Patent Literatures 1 to 3 The contents of Mg in the aluminum alloy materials described in the above Patent Literatures 1 to 3 are increased to an amount of not less than 5% by weight to make the aluminum alloy material stronger. However, Patent Literatures 1 to 3 do not give any consideration to strength anisotropy of the aluminum alloy materials.
  • an end product In a case where an aluminum alloy material has high strength anisotropy, an end product has low rigidity in a particular direction, so that the reliability of the end product could decrease. In addition, failure in dimension accuracy or other accuracy could occur in a production process such as press forming.
  • an aluminum alloy material (H tempered material) having an increased strength through working and curing has a problem of being prone to have remarkable strength anisotropy compared to an aluminum alloy material (O tempered material) which has been annealed.
  • an aluminum alloy material in accordance with an aspect of the present invention contains Mg: 7.0% to 10.0% (% by mass, the same applies hereinafter) and Ca: not more than 0.1%, the aluminum alloy material containing a remainder constituted by aluminum and an inevitable impurity, and the aluminum alloy material having a tensile strength of not less than 500 MPa and an elongation of not less than 3% and less than 10%.
  • An aspect of the present invention makes it possible to produce an aluminum alloy material which has both high strength and reduced strength anisotropy.
  • Fig. 1 is a view illustrating measurement directions of tensile strengths of an aluminum alloy material in the present embodiment.
  • the inventors of the present invention diligently investigated and studied alloy composition and metal structure which enable reduction in the strength anisotropy of a high-strength aluminum alloy material containing Mg (magnesium) in a large amount.
  • the inventors eventually found that it is possible to reduce the strength anisotropy by controlling an appropriate metal structure through adjustments to the alloy composition and to a production process.
  • Mg manganesium
  • the content of Mg in the aluminum alloy being not less than 7.0% makes it possible to sufficiently obtain the effect of improving strength.
  • the content of Mg in the aluminum alloy exceeding 10.0% causes occurrence of cracking during hot rolling, and thus could lead to difficulty in production. Accordingly, the content of Mg in the aluminum alloy is preferably in a range of not less than 7.5% and not more than 9.0%, and more preferably in a range of not less than 7.5% and not more than 8.5%.
  • Ca (Calcium) is present in the aluminum alloy mainly in the form of a compound. Even trace amounts of Ca cause cracking during hot working, and thus could lower workability.
  • the content of Ca in the aluminum alloy being not more than 0.1% makes it possible to prevent cracking during hot working.
  • the content of Ca in the aluminum alloy is more preferably not more than 0.05%.
  • Si forms mainly second phase particles (for example, single Si, Al-Si-Fe-Mn-based compound), and has an effect of making crystal grains finer by acting as a nucleation site for recrystallization.
  • the content of Si in the aluminum alloy being not less than 0.02% makes it possible to successfully obtain the effect of making crystal grains finer.
  • the content of Si in the aluminum alloy exceeding 0.3% cause generation of a large amount of coarse second phase particles, and thus could lower the elongation of a produced aluminum alloy material. Accordingly, the content of Si in the aluminum alloy is preferably in a range of not less than 0.02% and not more than 0.2%, and more preferably in a range of not less than 0.02% and not more than 0.15%.
  • Fe (iron) is present mainly in the form of second phase particles (such as an Al-Fe-based compound), has an effect of making crystal grains finer by acting as a nucleation site for recrystallization.
  • the content of Fe in the aluminum alloy being not less than 0.02% makes it possible to obtain the effect of making crystal grains finer.
  • the content of Fe in the aluminum alloy exceeding 0.5% causes generation of a large amount of coarse second phase particles, and thus could lower the elongation of a produced aluminum alloy material. Accordingly, the content of Fe in the aluminum alloy is preferably in a range of not less than 0.02% and not more than 0.25%, and more preferably in a range of not less than 0.02% and not more than 0.2%.
  • Cu copper
  • the content of Cu in the aluminum alloy being not less than 0.05% makes it possible to sufficiently obtain the effect of improving strength.
  • the content of Cu in the aluminum alloy exceeding 1.0% causes occurrence of cracking during hot rolling, and thus could lead to difficulty in production. Accordingly, the content of Cu in the aluminum alloy is preferably in a range of not less than 0.05% and not more than 0.5%, and more preferably in a range of not less than 0.10% and not more than 0.3%.
  • Mn manganese
  • Al-Mn-based compound an Al-Mn-based compound
  • the content of Mn in the aluminum alloy being not less than 0.05% makes it possible to sufficiently obtain the effect of making crystal grains finer.
  • the content of Mn in the aluminum alloy exceeding 1.0% causes generation of a large amount of coarse second phase particles, and thus lower the elongation of a produced aluminum alloy material. Accordingly, the content of Mn in the aluminum alloy is preferably in a range of not less than 0.1% and not more than 0.5%, and more preferably in a range of not less than 0.15% and not more than 0.3%.
  • Cr chromium
  • V vanadium
  • Zr zirconium
  • second phase particles such as an Al-Fe-Mn-based compound, an Al-Cr-based compound, an Al-V-based compound, and an Al-Zr-based compound
  • the content of Cr or V in the aluminum alloy being not less than 0.05% or the content of Zr in the aluminum alloy being not less than 0.02% makes it possible to sufficiently obtain the effect of making crystal grains finer.
  • the content of Cr or V in the aluminum alloy exceeding 0.3%, or the content of Zr exceeding 0.2% causes generation of a large amount of coarse second phase particles, and thus could lower the elongation of a produced aluminum alloy material.
  • the content of Cr or V in the aluminum alloy is preferably not more than 0.2%.
  • the content of Zr in the aluminum alloy is preferably 0.1%.
  • the contents of Cr, V, and Zr in the aluminum alloy are not limited to the above respective contents, provided that at least one of Cr, V, and Zr is contained in the aluminum alloy.
  • Ti titanium inhibits the growth of a solidified phase of aluminum formed during casting and makes a cast structure finer, thus having an effect of preventing a defect such as cracking during casting.
  • an excessively high content of Ti in the aluminum alloy makes second phase particles coarse, and thus could decrease the elongation of a produced aluminum alloy material.
  • the content of Ti in the aluminum alloy being not more than 0.2% makes it possible to prevent a decrease in the elongation of the produced aluminum alloy material.
  • the content of Ti in the aluminum alloy is more preferably not more than 0.1%. Note that substances other than the elements described above are basically Al and an inevitable impurity.
  • the present embodiment enables production of an aluminum alloy material (H tempered material) having a tensile strength of not less than 500 MPa and an elongation of not less than 3% and less than 10%, by performing production treatments (which will be discussed later) on the aluminum alloy of the above composition.
  • H tempered material H tempered material
  • elongation not less than 3% and less than 10%
  • This makes it possible to prevent an end product from having poor strength due to the aluminum alloy having a tensile strength falling below 500 MPa. It is also possible to prevent the occurrence of a defect such as cracking during working on the end product due to the aluminum alloy having an elongation falling below 3%.
  • the tensile strength of the aluminum alloy material is more preferably not less than 550 MPa. Further, the elongation of the aluminum alloy material is more preferably not less than 5% and less than 10%.
  • an aluminum alloy material 1 of the present embodiment is set such that, in a plane defined by a rolling direction (a final working direction) during a final rolling using a set of rolls 2 and a transverse direction, a standard deviation of tensile strengths is not more than 20 [MPa], wherein the tensile strengths are: a tensile strength in a 0° direction forming an angle of 0° with the rolling direction toward the transverse direction, a tensile strength in a 45° direction forming an angle of 45° with the rolling direction toward the transverse direction, and a tensile strength in a 90° direction forming an angle of 90° with the rolling direction towards the transverse direction.
  • the standard deviation of the tensile strengths of the aluminum alloy material 1 is preferably not more than 15 [MPa], and more preferably not more than 12 [MPa].
  • the aluminum alloy material of the present embodiment is set to have a ⁇ 013 ⁇ 100> orientation density and a ⁇ 011 ⁇ 100> orientation density which are calculated using a Crystallite Orientation Distribution Function (ODF) and which are each not more than 5 (for example, approximately 1).
  • ODF Crystallite Orientation Distribution Function
  • the aluminum alloy material of the present embodiment is set to have a ⁇ 011 ⁇ 211 > orientation density calculated using the crystallite orientation distribution function (ODF) such that a ratio obtained by dividing the ⁇ 011 ⁇ 211 > orientation density by a ⁇ 112 ⁇ 111> orientation density is not less than 0.4.
  • ODF crystallite orientation distribution function
  • the following description will discuss a method for producing the aluminum alloy material in accordance with the present embodiment.
  • the method for producing the aluminum alloy material of the present embodiment is carried out in the order of a casting step, a homogenization step, a hot rolling step, a cold rolling step, and an anneal step. Steps of the production method are not limited to these steps, which are illustrated by way of example.
  • a slab is casted in the casting step by a semi-continuous casting process such as a Direct Chill (DC) casting process and a hot top process.
  • the casting speed in the casting step is preferably 20 mm/min to 100 mm/min to prevent formation of coarse second phase particles.
  • the treatment temperature is set to not less than 400°C and not more than 490°C. This is because (i) the treatment temperature being not more than 400°C could cause insufficient homogenization, and (ii) the treatment temperature exceeding 490°C could cause melting of an AI-Mg-based compound remaining without dissolving as a solid solution, and thus cause a defect such as cracking during the hot rolling. Further, coarsening of second phase particles excessively progresses, and crystal grains in a particular orientation tend to preferentially grow in the subsequent recrystallization process, so that the strength anisotropy could decrease.
  • a two-stage homogenization treatment may be carried out.
  • the treatment temperature for the first stage is set to not less than 400°C and not more than 450°C. This is because (i) the treatment temperature for the first stage being not more than 400°C could cause insufficient homogenization, and (ii) the treatment temperature for the first stage exceeding 450°C could cause melting of an AI-Mg-based compound remaining without dissolving as a solid solution, and thus cause a defect such as cracking during the hot rolling.
  • the treatment time for the first stage is set to be in a range of not less than five hours and not more than 20 hours. This is because (i) the treatment time for the first stage being less than five hours causes insufficient homogenization, and (ii) the treatment time for the first stage exceeding 20 hours causes decrease in productivity. Carrying out the homogenization treatment in the first stage with the treatment temperature and the treatment time being appropriately set as described above makes it possible to cause the AI-Mg-based compound to dissolve as a solid solution, and thus enables homogenization at a higher temperature.
  • the treatment temperature for the second stage is set to not less than 450°C and not more than 490°C. This is because (i) the treatment temperature for the second stage being less than 450°C causes insufficient homogenization, and (ii) the treatment temperature for the second stage exceeding 490°C causes oxidization of Mg on the surface to progress and thus could decrease concentration of Mg on the surface.
  • the treatment time for the second stage is set to be in a range of not less than five hours and not more than 20 hours. This is because (i) the treatment time for the second stage being less than five hours causes insufficient homogenization, and (ii) the treatment time for the second stage exceeding 20 hours causes coarsening of second phase particles to excessively progress, causes crystal grains in a particular orientation to tend to preferentially grow in the subsequent recrystallization process, and thus could decrease the strength anisotropy.
  • the hot rolling step is carried out.
  • the starting temperature for the hot rolling is set to be in a range of not less than 350°C and not more than 480°C. This is because (i) the treatment temperature for the hot rolling being less than 350°C could make the rolling difficult due to excessively high deformation resistance, and (ii) the treatment temperature for the hot rolling exceeding 480°C causes the material to partially melt, and thus could lead to the occurrence of cracking. Note that the hot rolling step may be carried out with the homogenization step omitted.
  • the cold rolling step is carried out.
  • the cold rolling is carried out such that a rolling reduction from the plate thickness at the time of completion of the hot rolling step to the plate thickness at the time of completion of the cold rolling step (a ratio of a plate thickness after working to a plate thickness before the working) is not less than 50%.
  • the rolling reduction only needs to be not less than 50%, and may be changed as appropriate.
  • an intermediate annealing may be carried out before or in the middle of the cold rolling step.
  • the cold rolling is also carried out such that the rolling reduction from the plate thickness at the time of completion of the intermediate annealing to the plate thickness at the time of completion of the cold rolling is not less than 50%.
  • a treatment temperature for the intermediate annealing is preferably in a range of not less than 300°C and not more than 400°C.
  • a retention time for the intermediate annealing is preferably in a range of not less than one hour and not more than 10 hours. This is because carrying out the intermediate annealing at a high temperature for a long time could cause deterioration in appearance quality due to progression of oxidization on the surface.
  • the aluminum alloy material of the present embodiment described above it is possible to produce an aluminum alloy material having both high strength and reduced strength anisotropy by appropriately controlling the metal structure through adjustments to the composition of the aluminum alloy and the production process for the aluminum alloy. This enables improvement in productivity of the aluminum alloy material and improvement in reliability of an end product.
  • Example 1 of the present embodiment will discuss Example 1 of the present embodiment with reference to Table 1 and Table 2.
  • Table 1 shows the composition of the aluminum alloy used in Example 1.
  • the composition of the aluminum alloy of Example 1 is within a predetermined range.
  • the prdetermined range means that the content of Mg is in a range of 7.0% to 10.0%, and the content of Ca is in a range of not more than 0.1%.
  • the homogenization step, the hot rolling step, and the cold rolling step are carried out.
  • the plate thickness of the aluminum alloy material after completion of the cold rolling step is assumed to be 1.0 mm.
  • Example 1 heating at 465°C for 12 hours is carried out in the homogenization step prior to the hot rolling step.
  • the rolling reduction from the plate thickness at the time of completion of the hot rolling to the plate thickness at the time of completion of the cold rolling is assumed to be 80%.
  • Table 2 shows the strength property, the strength anisotropy, and the productivity of an aluminum alloy material produced by performing the above treatment on the aluminum alloy of Example 1 having the composition shown in Table 1.
  • the aluminum alloy material produced in Example 1 has a tensile strength and an elongation within the respective predetermined ranges.
  • the aluminum alloy material produced in Example 1 has a tensile strength in a range of not less than 500 MPa and an elongation in a range of not less than 3% and less than 10%.
  • the tensile strength and the elongation of the produced aluminum alloy material are measured in conformity with JIS Z-2241-2011.
  • tensile strengths and elongations of the produced aluminum alloy material 1 are measured in a 0° direction, which is the rolling direction, in a 45° direction forming an angle of 45° with the 0° direction from the rolling direction toward the transverse direction, and in a 90° direction forming an angle of 90° with the 0° direction from the rolling direction toward the transverse direction.
  • the tensile strength and the elongation of the produced aluminum alloy material 1 are defined respectively as the average value for the measured tensile strengths and the average value for the measured elongations.
  • Tensile strengths are measured, in the plane defined by the rolling direction (final working direction) and the transverse direction, in the 0° direction, which is the rolling direction, in the 45° direction forming an angle of 45° with the 0° direction from the rolling direction toward the transverse direction, and in the 90° direction forming an angle of 90° with the 0° direction from the rolling direction toward the transverse direction.
  • the strength anisotropy is defined as a standard deviation [MPa] calculated by using the following Formula (1).
  • TS i [MPa] represents a tensile strength of each direction
  • TS [MPa] represents the average value for the tensile strengths in the respective directions
  • n represents the total number of pieces of the tensile strength data.
  • the three-dimensional orientation analyzing method using the crystallite orientation distribution function (ODF) described above is applied to the aluminum alloy material of Example 1 to calculate an orientation density. Specifically, a cross section of a portion of the produced aluminum alloy material in a plane perpendicular to the working direction (rolling direction) of the aluminum alloy material is measured with an X-ray diffractometry. In this measurement, after incomplete pole figures of the (111), (220), and (200) planes are measured using the above Schlz reflection method in an inclination angle range of 15 degrees to 90 degrees, a series expansion is performed to determine the crystallite orientation distribution function (ODF).
  • ODF crystallite orientation distribution function
  • the orientation density of each orientation thus obtained is calculated as a ratio with respect to the orientation density of a standard sample having a random crystallographic texture.
  • Table 2 shows results of evaluations performed such that an aluminum alloy material having a ⁇ 013 ⁇ 100> orientation density of not more than 5 and a ⁇ 011 ⁇ 100> orientation density of not more than 5 is rated as "G (good)", and an aluminum alloy material having a ⁇ 013 ⁇ 100> orientation density exceeding 5 and a ⁇ 011 ⁇ 100> orientation density exceeding 5 is rated as "P (poor)".
  • an aluminum alloy material having a ratio obtained by dividing a ⁇ 011 ⁇ 211> orientation density by a ⁇ 112 ⁇ 111> orientation density of not less than 0.4 is rated as "G”
  • an aluminum alloy material having a ratio obtained by dividing a ⁇ 011 ⁇ 211> orientation density by a ⁇ 112 ⁇ 111> orientation density falling below 0.4 is rated as "P”.
  • Example 1 successfully reduced strength anisotropy.
  • Example 1 shows the results that indicate no problem with productivity.
  • Table 4 shows properties of aluminum alloy materials produced by performing a treatment similar to that for Example 1 on aluminum alloys of Comparative Example 1 to Comparative Example 5 having their respective compositions shown in Table 3. Note that, for Comparative Examples 1 to 3, a treatment at 500°C and for eight hours was performed as the homogenization treatment.
  • Comparative Example 1 in which the content of Mg is too low, results in a produced aluminum alloy material having a tensile strength falling below the predetermined range, and thus fails to yield good mechanical properties.
  • Comparative Example 2 in which the content of Mg is too low, results in a produced aluminum alloy material having a tensile strength falling below the predetermined range, and thus fails to yield good mechanical properties. Further, since the homogenization treatment temperature is too high, the strength anisotropy exceeds the predetermined range, so that Comparative Example 2 fails to yield good mechanical properties.
  • Comparative Example 3 in which the content of Mg is too low, results in a produced aluminum alloy material having a tensile strength falling below the predetermined range, and thus fails to yield good mechanical properties.
  • Comparative Example 4 in which the content of Mg is too high, causes occurrence of cracking during the hot rolling. This makes rolling difficult, so that the production is impossible.
  • Comparative Example 5 in which the content of Ca is too high, causes occurrence of cracking during the hot rolling. This makes rolling difficult, so that the production is impossible.
  • An aluminum alloy material in accordance with an aspect of the present invention contains Mg: 7.0% to 10.0% (% by mass, the same applies hereinafter) and Ca: not more than 0.1%, the aluminum alloy material containing a remainder being constituted by aluminum and an inevitable impurity, the aluminum alloy material having a tensile strength of not less than 500 MPa and an elongation of not less than 3% and less than 10%.
  • the aluminum alloy material preferably contains Mn: 0.05% to 1.0%.
  • the aluminum alloy material has a standard deviation of tensile strengths of not more than 20, in a plane defined by a final working direction and a transverse direction of the aluminum alloy material, wherein the tensile strengths are a tensile strength in a 0° direction, which is the final working direction, a tensile strength in a 45° direction forming an angle of 45° with the 0° direction from the final working direction toward the transverse direction, and a tensile strength in a 90° direction forming an angle of 90° with the 0° direction from the final working direction toward the transverse direction.
  • the aluminum alloy material preferably has a ⁇ 013 ⁇ 100> orientation density of not more than 5 and a ⁇ 011 ⁇ 100> orientation density of not more than 5, wherein the ⁇ 013 ⁇ 100> orientation density and the ⁇ 011 ⁇ 100> orientation density are calculated using a crystallite orientation distribution function (ODF).
  • ODF crystallite orientation distribution function
  • the aluminum alloy material preferably has a ⁇ 011 ⁇ 211> orientation density which is not less than 0.4 times a ⁇ 112 ⁇ 111> orientation density, wherein the ⁇ 011 ⁇ 211> orientation density is calculated using a crystallite orientation distribution function (ODF).
  • ODF crystallite orientation distribution function

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Mechanical Engineering (AREA)
  • Materials Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Physics & Mathematics (AREA)
  • Thermal Sciences (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Metal Rolling (AREA)

Abstract

An aluminum alloy material contains Mg: 7.0% to 10.0% (% by mass, the same applies hereinafter) and Ca: not more than 0.1%, and the aluminum alloy material contains a remainder constituted by aluminum and an inevitable impurity. The aluminum alloy material has a tensile strength of not less than 500 MPa and an elongation of not less than 3% and less than 10%.

Description

    Technical Field
  • The present invention relates to a high-strength aluminum alloy material having reduced strength anisotropy.
  • Background Art
  • Recently, there has been a demand for using an aluminum alloy material to make stronger and lighter various products including, for example, a housing of an electrical device. Using an aluminum alloy material having higher strength makes it possible to reduce the amount of usage of the aluminum alloy material while maintaining the strength of the products at the same degree as before, and thus enables reduction in the weights of the products.
  • Typical high-strength aluminum alloys include, for example, a 6000 series alloy and a 7000 series alloy. However, the above-described alloys are heat-treatable alloys, which require solution treatment and aging heat treatment, and thus have a problem of low production efficiency. In addition, the 7000 series alloy contains Zn and Cu in a large amount, and thus have a problem of causing corrosion to easily occur depending on usage environments.
  • In view of the above, non-heat-treatable aluminum alloys are used in some cases. Typical non-heat-treatable aluminum alloys include a 5000 series alloy, which has the highest strength. The 5000 series alloy, which typically has excellent corrosion resistance, does not require the solution treatment and the aging heat treatment, so that the 5000 series alloy is produced with high efficiency. Further, increase in the amount of an element added to the 5000 series alloy makes it possible to achieve the 5000 series alloy having strength not less than that of a 6000 series alloy. For the above reasons, proposed is a 5000 series aluminum alloy material containing not less than 5% by weight of Mg, which is a major additive element (see Patent Literatures 1 to 3).
  • Citation List
    • [Patent Literature 1]
      Japanese Patent Application Publication, Tokukai, No. 2007-186747
    • [Patent Literature 2]
      Japanese Patent Application Publication, Tokukai, No. 2001-98338
    • [Patent Literature 3]
      Japanese Patent Application Publication, Tokukaihei, No. 7-197170
    Summary of Invention Technical Problem
  • The contents of Mg in the aluminum alloy materials described in the above Patent Literatures 1 to 3 are increased to an amount of not less than 5% by weight to make the aluminum alloy material stronger. However, Patent Literatures 1 to 3 do not give any consideration to strength anisotropy of the aluminum alloy materials.
  • In a case where an aluminum alloy material has high strength anisotropy, an end product has low rigidity in a particular direction, so that the reliability of the end product could decrease. In addition, failure in dimension accuracy or other accuracy could occur in a production process such as press forming. In particular, an aluminum alloy material (H tempered material) having an increased strength through working and curing has a problem of being prone to have remarkable strength anisotropy compared to an aluminum alloy material (O tempered material) which has been annealed.
  • It is an object of an aspect of the present invention, which has been made to solve the above problem, to provide an aluminum alloy material which has both high strength and reduced strength anisotropy, by controlling the metal structure.
  • Solution to Problem
  • To solve the above problems, an aluminum alloy material in accordance with an aspect of the present invention contains Mg: 7.0% to 10.0% (% by mass, the same applies hereinafter) and Ca: not more than 0.1%, the aluminum alloy material containing a remainder constituted by aluminum and an inevitable impurity, and the aluminum alloy material having a tensile strength of not less than 500 MPa and an elongation of not less than 3% and less than 10%.
  • Advantageous Effects of Invention
  • An aspect of the present invention makes it possible to produce an aluminum alloy material which has both high strength and reduced strength anisotropy.
  • Brief Description of Drawings
  • Fig. 1 is a view illustrating measurement directions of tensile strengths of an aluminum alloy material in the present embodiment.
  • Description of Embodiments
  • The inventors of the present invention diligently investigated and studied alloy composition and metal structure which enable reduction in the strength anisotropy of a high-strength aluminum alloy material containing Mg (magnesium) in a large amount. The inventors eventually found that it is possible to reduce the strength anisotropy by controlling an appropriate metal structure through adjustments to the alloy composition and to a production process.
  • The following description will discuss an aluminum alloy material in accordance with an embodiment of the present invention in detail. Note that it is assumed that the aluminum alloy material of the present embodiment is used for members of household electrical appliances, buildings, structures, transport equipment, and the like that are required to have strength and isotropy of strength. In the following description, the unit "% by mass" is abbreviated and written simply as "%".
  • (Elements Which Must Be Contained in Aluminum Alloy) [Mg]
  • Mg (magnesium) is present mainly in the form of a solid solution element, and has an effect of improving strength. The content of Mg in the aluminum alloy being not less than 7.0% makes it possible to sufficiently obtain the effect of improving strength.
  • However, the content of Mg in the aluminum alloy exceeding 10.0% causes occurrence of cracking during hot rolling, and thus could lead to difficulty in production. Accordingly, the content of Mg in the aluminum alloy is preferably in a range of not less than 7.5% and not more than 9.0%, and more preferably in a range of not less than 7.5% and not more than 8.5%.
  • [Ca]
  • Ca (Calcium) is present in the aluminum alloy mainly in the form of a compound. Even trace amounts of Ca cause cracking during hot working, and thus could lower workability. The content of Ca in the aluminum alloy being not more than 0.1% makes it possible to prevent cracking during hot working. The content of Ca in the aluminum alloy is more preferably not more than 0.05%.
  • (Elements Selectively Contained in Aluminum Alloy) [Si]
  • Si (silicon) forms mainly second phase particles (for example, single Si, Al-Si-Fe-Mn-based compound), and has an effect of making crystal grains finer by acting as a nucleation site for recrystallization. The content of Si in the aluminum alloy being not less than 0.02% makes it possible to successfully obtain the effect of making crystal grains finer.
  • However, the content of Si in the aluminum alloy exceeding 0.3% cause generation of a large amount of coarse second phase particles, and thus could lower the elongation of a produced aluminum alloy material. Accordingly, the content of Si in the aluminum alloy is preferably in a range of not less than 0.02% and not more than 0.2%, and more preferably in a range of not less than 0.02% and not more than 0.15%.
  • [Fe]
  • Fe (iron) is present mainly in the form of second phase particles (such as an Al-Fe-based compound), has an effect of making crystal grains finer by acting as a nucleation site for recrystallization. The content of Fe in the aluminum alloy being not less than 0.02% makes it possible to obtain the effect of making crystal grains finer.
  • However, the content of Fe in the aluminum alloy exceeding 0.5% causes generation of a large amount of coarse second phase particles, and thus could lower the elongation of a produced aluminum alloy material. Accordingly, the content of Fe in the aluminum alloy is preferably in a range of not less than 0.02% and not more than 0.25%, and more preferably in a range of not less than 0.02% and not more than 0.2%.
  • [Cu]
  • Cu (copper) is present mainly in the form of a solid solution element, and has an effect of improving strength. The content of Cu in the aluminum alloy being not less than 0.05% makes it possible to sufficiently obtain the effect of improving strength.
  • However, the content of Cu in the aluminum alloy exceeding 1.0% causes occurrence of cracking during hot rolling, and thus could lead to difficulty in production. Accordingly, the content of Cu in the aluminum alloy is preferably in a range of not less than 0.05% and not more than 0.5%, and more preferably in a range of not less than 0.10% and not more than 0.3%.
  • [Mn]
  • Mn (manganese) is present mainly in the form of second phase particles (an Al-Mn-based compound), and has an effect of making crystal grains finer by acting as a nucleation site for recrystallization. Specifically, the content of Mn in the aluminum alloy being not less than 0.05% makes it possible to sufficiently obtain the effect of making crystal grains finer.
  • However, the content of Mn in the aluminum alloy exceeding 1.0% causes generation of a large amount of coarse second phase particles, and thus lower the elongation of a produced aluminum alloy material. Accordingly, the content of Mn in the aluminum alloy is preferably in a range of not less than 0.1% and not more than 0.5%, and more preferably in a range of not less than 0.15% and not more than 0.3%.
  • [Cr, V, Zr]
  • Cr (chromium), V (vanadium), and Zr (zirconium) are present mainly in the form of second phase particles (such as an Al-Fe-Mn-based compound, an Al-Cr-based compound, an Al-V-based compound, and an Al-Zr-based compound), and have an effect of making crystal grains finer by acting as a nucleation site for recrystallization. Specifically, the content of Cr or V in the aluminum alloy being not less than 0.05% or the content of Zr in the aluminum alloy being not less than 0.02% makes it possible to sufficiently obtain the effect of making crystal grains finer.
  • However, the content of Cr or V in the aluminum alloy exceeding 0.3%, or the content of Zr exceeding 0.2% causes generation of a large amount of coarse second phase particles, and thus could lower the elongation of a produced aluminum alloy material.
  • Accordingly, the content of Cr or V in the aluminum alloy is preferably not more than 0.2%. In addition, the content of Zr in the aluminum alloy is preferably 0.1%.
  • The contents of Cr, V, and Zr in the aluminum alloy are not limited to the above respective contents, provided that at least one of Cr, V, and Zr is contained in the aluminum alloy.
  • [Ti]
  • Ti (titanium) inhibits the growth of a solidified phase of aluminum formed during casting and makes a cast structure finer, thus having an effect of preventing a defect such as cracking during casting. However, an excessively high content of Ti in the aluminum alloy makes second phase particles coarse, and thus could decrease the elongation of a produced aluminum alloy material.
  • In light of the above, the content of Ti in the aluminum alloy being not more than 0.2% makes it possible to prevent a decrease in the elongation of the produced aluminum alloy material. The content of Ti in the aluminum alloy is more preferably not more than 0.1%. Note that substances other than the elements described above are basically Al and an inevitable impurity.
  • (Tensile Strength and Elongation)
  • The present embodiment enables production of an aluminum alloy material (H tempered material) having a tensile strength of not less than 500 MPa and an elongation of not less than 3% and less than 10%, by performing production treatments (which will be discussed later) on the aluminum alloy of the above composition. This makes it possible to prevent an end product from having poor strength due to the aluminum alloy having a tensile strength falling below 500 MPa. It is also possible to prevent the occurrence of a defect such as cracking during working on the end product due to the aluminum alloy having an elongation falling below 3%.
  • The tensile strength of the aluminum alloy material is more preferably not less than 550 MPa. Further, the elongation of the aluminum alloy material is more preferably not less than 5% and less than 10%.
  • (Strength Anisotropy)
  • As illustrated in Fig. 1, an aluminum alloy material 1 of the present embodiment is set such that, in a plane defined by a rolling direction (a final working direction) during a final rolling using a set of rolls 2 and a transverse direction, a standard deviation of tensile strengths is not more than 20 [MPa], wherein the tensile strengths are: a tensile strength in a 0° direction forming an angle of 0° with the rolling direction toward the transverse direction, a tensile strength in a 45° direction forming an angle of 45° with the rolling direction toward the transverse direction, and a tensile strength in a 90° direction forming an angle of 90° with the rolling direction towards the transverse direction. This setting is made in consideration of the fact that the standard deviation of the tensile strengths exceeding 20 [MPa], which means an excessively high strength anisotropy, decreases the strength in a particular direction of an end product and could decrease the reliability of the end product. The standard deviation of the tensile strengths is calculated by using Formula (1) (which will be described later).
  • The standard deviation of the tensile strengths of the aluminum alloy material 1 is preferably not more than 15 [MPa], and more preferably not more than 12 [MPa].
  • (Crystallographic Texture)
  • The aluminum alloy material of the present embodiment is set to have a {013}<100> orientation density and a {011}<100> orientation density which are calculated using a Crystallite Orientation Distribution Function (ODF) and which are each not more than 5 (for example, approximately 1). This setting is made in consideration of the fact that the {013}<100> orientation density and the {011}<100> orientation density both exceeding 5 makes the strength anisotropy remarkable and thus could decrease the strength of an end product in a particular direction.
  • In addition, the aluminum alloy material of the present embodiment is set to have a {011}<211 > orientation density calculated using the crystallite orientation distribution function (ODF) such that a ratio obtained by dividing the {011}<211 > orientation density by a {112}<111> orientation density is not less than 0.4. Such a setting is made in consideration of the fact that the {011}<211> orientation density being less than 0.4 times the {112}<111 > orientation density makes the strength anisotropy remarkable and thus could decrease the strength of an end product in a particular direction.
  • Now, a method for calculating an orientation density using the crystallite orientation distribution function (ODF) will be described in detail. In the present embodiment, a three-dimensional orientation analyzing method (see, Journal of Japan Institute of Light Metals, 1992, volume 42, No. 6, pp. 358 to 367) using the crystallite orientation distribution function (ODF) is applied to a produced aluminum alloy material to calculate an orientation density. First, a cross section of the aluminum alloy material perpendicular to the working direction (rolling direction) is measured by an X-ray diffractometry. In this measurement, incomplete pole figures of (111), (220), and (200) planes are measured in an inclination angle range of 15 degrees to 90 degrees, using the Schlz reflection method (see, Journal of Japan Institute of Light Metals, 1983, volume 33, No. 4, pp. 230 to 239). Next, the crystallite orientation distribution function (ODF) is determined through a series expansion. From this, an orientation density of each orientation is calculated as a ratio with respect to the orientation density of a standard sample having random crystallographic texture.
  • (Method for Producing Aluminum Alloy Material)
  • The following description will discuss a method for producing the aluminum alloy material in accordance with the present embodiment. The method for producing the aluminum alloy material of the present embodiment is carried out in the order of a casting step, a homogenization step, a hot rolling step, a cold rolling step, and an anneal step. Steps of the production method are not limited to these steps, which are illustrated by way of example.
  • First, a slab is casted in the casting step by a semi-continuous casting process such as a Direct Chill (DC) casting process and a hot top process. The casting speed in the casting step is preferably 20 mm/min to 100 mm/min to prevent formation of coarse second phase particles.
  • Upon completion of the casting step, the homogenization step is carried out. The treatment temperature is set to not less than 400°C and not more than 490°C. This is because (i) the treatment temperature being not more than 400°C could cause insufficient homogenization, and (ii) the treatment temperature exceeding 490°C could cause melting of an AI-Mg-based compound remaining without dissolving as a solid solution, and thus cause a defect such as cracking during the hot rolling. Further, coarsening of second phase particles excessively progresses, and crystal grains in a particular orientation tend to preferentially grow in the subsequent recrystallization process, so that the strength anisotropy could decrease.
  • In the homogenization step of the present embodiment, a two-stage homogenization treatment may be carried out. In that case, the treatment temperature for the first stage is set to not less than 400°C and not more than 450°C. This is because (i) the treatment temperature for the first stage being not more than 400°C could cause insufficient homogenization, and (ii) the treatment temperature for the first stage exceeding 450°C could cause melting of an AI-Mg-based compound remaining without dissolving as a solid solution, and thus cause a defect such as cracking during the hot rolling.
  • Further, the treatment time for the first stage is set to be in a range of not less than five hours and not more than 20 hours. This is because (i) the treatment time for the first stage being less than five hours causes insufficient homogenization, and (ii) the treatment time for the first stage exceeding 20 hours causes decrease in productivity. Carrying out the homogenization treatment in the first stage with the treatment temperature and the treatment time being appropriately set as described above makes it possible to cause the AI-Mg-based compound to dissolve as a solid solution, and thus enables homogenization at a higher temperature.
  • Subsequently, the treatment temperature for the second stage is set to not less than 450°C and not more than 490°C. This is because (i) the treatment temperature for the second stage being less than 450°C causes insufficient homogenization, and (ii) the treatment temperature for the second stage exceeding 490°C causes oxidization of Mg on the surface to progress and thus could decrease concentration of Mg on the surface.
  • Further, the treatment time for the second stage is set to be in a range of not less than five hours and not more than 20 hours. This is because (i) the treatment time for the second stage being less than five hours causes insufficient homogenization, and (ii) the treatment time for the second stage exceeding 20 hours causes coarsening of second phase particles to excessively progress, causes crystal grains in a particular orientation to tend to preferentially grow in the subsequent recrystallization process, and thus could decrease the strength anisotropy.
  • Next, the hot rolling step is carried out. In the hot rolling step, the starting temperature for the hot rolling is set to be in a range of not less than 350°C and not more than 480°C. This is because (i) the treatment temperature for the hot rolling being less than 350°C could make the rolling difficult due to excessively high deformation resistance, and (ii) the treatment temperature for the hot rolling exceeding 480°C causes the material to partially melt, and thus could lead to the occurrence of cracking. Note that the hot rolling step may be carried out with the homogenization step omitted.
  • Subsequently, upon completion of the hot rolling step, the cold rolling step is carried out. In the cold rolling step, the cold rolling is carried out such that a rolling reduction from the plate thickness at the time of completion of the hot rolling step to the plate thickness at the time of completion of the cold rolling step (a ratio of a plate thickness after working to a plate thickness before the working) is not less than 50%. The rolling reduction only needs to be not less than 50%, and may be changed as appropriate.
  • Note that an intermediate annealing may be carried out before or in the middle of the cold rolling step. In this case, the cold rolling is also carried out such that the rolling reduction from the plate thickness at the time of completion of the intermediate annealing to the plate thickness at the time of completion of the cold rolling is not less than 50%. A treatment temperature for the intermediate annealing is preferably in a range of not less than 300°C and not more than 400°C. Further, a retention time for the intermediate annealing is preferably in a range of not less than one hour and not more than 10 hours. This is because carrying out the intermediate annealing at a high temperature for a long time could cause deterioration in appearance quality due to progression of oxidization on the surface.
  • According to the aluminum alloy material of the present embodiment described above, it is possible to produce an aluminum alloy material having both high strength and reduced strength anisotropy by appropriately controlling the metal structure through adjustments to the composition of the aluminum alloy and the production process for the aluminum alloy. This enables improvement in productivity of the aluminum alloy material and improvement in reliability of an end product.
  • Examples
  • The following description will discuss Example 1 of the present embodiment with reference to Table 1 and Table 2.
  • (Composition of Aluminum Alloy)
  • Table 1 shows the composition of the aluminum alloy used in Example 1.
  • [Table 1]
  • (Table 1)
    Present Invention Composition of Aluminum Alloy [% by Mass]
    Fe Si Cu Mn Mg Cr Ti V Zr Ca Al
    Example 1 0.22 0.10 <0.01 0.40 7.6 0.02 0.03 0.01 <0.01 <0.01 Remaining Percentage
  • As shown in Table 1, the composition of the aluminum alloy of Example 1 is within a predetermined range. The prdetermined range means that the content of Mg is in a range of 7.0% to 10.0%, and the content of Ca is in a range of not more than 0.1%.
  • (Production Method)
  • After the aluminum alloy having the composition shown in Table 1 is molten and is subjected to the DC casting, the homogenization step, the hot rolling step, and the cold rolling step are carried out. The plate thickness of the aluminum alloy material after completion of the cold rolling step is assumed to be 1.0 mm.
  • In Example 1, heating at 465°C for 12 hours is carried out in the homogenization step prior to the hot rolling step. In the cold rolling step, the rolling reduction from the plate thickness at the time of completion of the hot rolling to the plate thickness at the time of completion of the cold rolling is assumed to be 80%.
  • (Property of Aluminum Alloy Material)
  • Table 2 shows the strength property, the strength anisotropy, and the productivity of an aluminum alloy material produced by performing the above treatment on the aluminum alloy of Example 1 having the composition shown in Table 1.
  • [Table 2]
  • (Table 2)
    Present Invention Strength Property Anisotropy Productivity
    Tensile Strength [MPa] Elongation [%] Strength Anisotropy [MPa] {013}<100> Orientation Density {011}<100> Orientation Density Orientation Density Ratio of {011}<211> /{0 11}<1 00>
    Example 1 572 8 10 G G G G
  • (Tensile Strength and Elongation)
  • As shown in Table 2, the aluminum alloy material produced in Example 1 has a tensile strength and an elongation within the respective predetermined ranges. In other words, the aluminum alloy material produced in Example 1 has a tensile strength in a range of not less than 500 MPa and an elongation in a range of not less than 3% and less than 10%.
  • Note that the tensile strength and the elongation of the produced aluminum alloy material are measured in conformity with JIS Z-2241-2011. As illustrated in Fig. 1, in a plane defined by a rolling direction along which the set of rolls 2 moves (final working direction) and a transverse direction, tensile strengths and elongations of the produced aluminum alloy material 1 are measured in a 0° direction, which is the rolling direction, in a 45° direction forming an angle of 45° with the 0° direction from the rolling direction toward the transverse direction, and in a 90° direction forming an angle of 90° with the 0° direction from the rolling direction toward the transverse direction. The tensile strength and the elongation of the produced aluminum alloy material 1 are defined respectively as the average value for the measured tensile strengths and the average value for the measured elongations.
  • (Strength Anisotropy)
  • Tensile strengths are measured, in the plane defined by the rolling direction (final working direction) and the transverse direction, in the 0° direction, which is the rolling direction, in the 45° direction forming an angle of 45° with the 0° direction from the rolling direction toward the transverse direction, and in the 90° direction forming an angle of 90° with the 0° direction from the rolling direction toward the transverse direction. The strength anisotropy is defined as a standard deviation [MPa] calculated by using the following Formula (1). l = 1 n TS i TS 2 n 1 n 2
    Figure imgb0001
  • In the formula, TSi [MPa] represents a tensile strength of each direction, TS [MPa] represents the average value for the tensile strengths in the respective directions, and n represents the total number of pieces of the tensile strength data.
  • (Crystallographic Texture)
  • The three-dimensional orientation analyzing method using the crystallite orientation distribution function (ODF) described above is applied to the aluminum alloy material of Example 1 to calculate an orientation density. Specifically, a cross section of a portion of the produced aluminum alloy material in a plane perpendicular to the working direction (rolling direction) of the aluminum alloy material is measured with an X-ray diffractometry. In this measurement, after incomplete pole figures of the (111), (220), and (200) planes are measured using the above Schlz reflection method in an inclination angle range of 15 degrees to 90 degrees, a series expansion is performed to determine the crystallite orientation distribution function (ODF).
  • The orientation density of each orientation thus obtained is calculated as a ratio with respect to the orientation density of a standard sample having a random crystallographic texture. Table 2 shows results of evaluations performed such that an aluminum alloy material having a {013}<100> orientation density of not more than 5 and a {011}<100> orientation density of not more than 5 is rated as "G (good)", and an aluminum alloy material having a {013}<100> orientation density exceeding 5 and a {011}<100> orientation density exceeding 5 is rated as "P (poor)". Further, an aluminum alloy material having a ratio obtained by dividing a {011}<211> orientation density by a {112}< 111> orientation density of not less than 0.4 is rated as "G", and an aluminum alloy material having a ratio obtained by dividing a {011}<211> orientation density by a {112}<111> orientation density falling below 0.4 is rated as "P".
  • As shown in Table 2, it is understood that Example 1 successfully reduced strength anisotropy. In addition, Example 1 shows the results that indicate no problem with productivity.
  • (Comparative Examples)
  • As comparative examples to Example 1 described above, Table 4 shows properties of aluminum alloy materials produced by performing a treatment similar to that for Example 1 on aluminum alloys of Comparative Example 1 to Comparative Example 5 having their respective compositions shown in Table 3. Note that, for Comparative Examples 1 to 3, a treatment at 500°C and for eight hours was performed as the homogenization treatment.
  • [Table 3]
  • (Table 3)
    Comparative Example Composition of Aluminum Alloy [% by Mass]
    Fe Si Cu Mn Mg Cr Ti V Zr Ca Al
    Comparative Example 1 0.16 0.07 0.08 <0.01 6.8 <0.01 0.01 <0.01 <0.01 <0.01 Remaining Percentage
    Comparative Example 2 0.16 0.07 0.08 0.24 6.7 <0.01 0.01 <0.01 <0.01 <0.01 Remaining Percentage
    Comparative Example 3 0.16 0.07 0.08 <0.01 5.7 0.20 0.01 <0.01 <0.01 <0.01 Remaining Percentage
    Comparative Example 4 0.16 0.07 0.08 <0.01 11.0 <0.01 0.01 <0.01 <0.01 <0.01 Remaining Percentage
    Comparative Example 5 0.16 0.07 0.08 <0.01 9.0 <0.01 0.01 <0.01 <0.01 0.50 Remaining Percentage
  • [Table 4]
  • (Table 4)
    Comparative Example Strength Property Anisotropy Productivity
    Tensile Strength [MPa] Elongation [%] Strength Anisotropy [MPa] {013}<100> Orientation Density {011}<100> Orientation Density Orientation Density Ratio of {011}<211>/{011}<100>
    Comparative Example 1 470 9 12 G G G G
    Comparative Example 2 487 9 21 G G P G
    Comparative Example 3 478 8 15 G G G G
    Comparative Example 4 - - - - - - P
    Comparative Example 5 - - - - - - P
  • Comparative Example 1, in which the content of Mg is too low, results ina produced aluminum alloy material having a tensile strength falling below the predetermined range, and thus fails to yield good mechanical properties.
  • Comparative Example 2, in which the content of Mg is too low, results in a produced aluminum alloy material having a tensile strength falling below the predetermined range, and thus fails to yield good mechanical properties. Further, since the homogenization treatment temperature is too high, the strength anisotropy exceeds the predetermined range, so that Comparative Example 2 fails to yield good mechanical properties.
  • Comparative Example 3, in which the content of Mg is too low, results in a produced aluminum alloy material having a tensile strength falling below the predetermined range, and thus fails to yield good mechanical properties.
  • Comparative Example 4, in which the content of Mg is too high, causes occurrence of cracking during the hot rolling. This makes rolling difficult, so that the production is impossible.
  • Comparative Example 5, in which the content of Ca is too high, causes occurrence of cracking during the hot rolling. This makes rolling difficult, so that the production is impossible.
  • The present invention is not limited to the embodiments, but can be altered by a skilled person in the art within the scope of the claims. An embodiment based on a proper combination of technical means disclosed in different embodiments is encompassed in the technical scope of the present invention.
  • An aluminum alloy material in accordance with an aspect of the present invention contains Mg: 7.0% to 10.0% (% by mass, the same applies hereinafter) and Ca: not more than 0.1%, the aluminum alloy material containing a remainder being constituted by aluminum and an inevitable impurity, the aluminum alloy material having a tensile strength of not less than 500 MPa and an elongation of not less than 3% and less than 10%.
  • The aluminum alloy material preferably contains Mn: 0.05% to 1.0%.
  • Further, the aluminum alloy material has a standard deviation of tensile strengths of not more than 20, in a plane defined by a final working direction and a transverse direction of the aluminum alloy material, wherein the tensile strengths are a tensile strength in a 0° direction, which is the final working direction, a tensile strength in a 45° direction forming an angle of 45° with the 0° direction from the final working direction toward the transverse direction, and a tensile strength in a 90° direction forming an angle of 90° with the 0° direction from the final working direction toward the transverse direction.
  • The aluminum alloy material preferably has a {013}<100> orientation density of not more than 5 and a {011}<100> orientation density of not more than 5, wherein the {013}<100> orientation density and the {011}<100> orientation density are calculated using a crystallite orientation distribution function (ODF).
  • The aluminum alloy material preferably has a {011}<211> orientation density which is not less than 0.4 times a {112}<111> orientation density, wherein the {011}<211> orientation density is calculated using a crystallite orientation distribution function (ODF).
  • Reference Signs List
  • 1
    aluminum alloy material
    2
    roll

Claims (5)

  1. An aluminum alloy material containing Mg: 7.0% to 10.0% (% by mass, the same applies hereinafter) and Ca: not more than 0.1%,
    - the aluminum alloy material containing a remainder being constituted by aluminum and an inevitable impurity,
    - the aluminum alloy material having a tensile strength of not less than 500 MPa and an elongation of not less than 3% and less than 10%.
  2. The aluminum alloy material according to Claim 1, wherein the aluminum alloy material contains Mn: 0.05% to 1.0%.
  3. The aluminum alloy material according to Claim 1 or 2, wherein the aluminum alloy material has a standard deviation of tensile strengths of not more than 20, in a plane defined by a final working direction and a transverse direction of the aluminum alloy material, wherein the tensile strengths are a tensile strength in a 0° direction, which is the final working direction, a tensile strength in a 45° direction forming an angle of 45° with the 0° direction from the final working direction toward the transverse direction, and a tensile strength in a 90° direction forming an angle of 90° with the 0° direction from the final working direction toward the transverse direction.
  4. The aluminum alloy material according to Claim 3, wherein the aluminum alloy material has a {013}<100> orientation density of not more than 5 and a {011}<100> orientation density of not more than 5, wherein the {013}<100> orientation density and the {011}<100> orientation density are calculated using a crystallite orientation distribution function (ODF).
  5. The aluminum alloy material according to Claim 3 or 4, wherein the aluminum alloy material has a {011}<211> orientation density which is not less than 0.4 times a {112}<111> orientation density, wherein the {011}<211 > orientation density is calculated using a crystallite orientation distribution function (ODF).
EP20874847.5A 2019-10-08 2020-10-08 Aluminum alloy material Pending EP4043602A4 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2019185298A JP7414452B2 (en) 2019-10-08 2019-10-08 Aluminum alloy material and its manufacturing method
PCT/JP2020/038086 WO2021070889A1 (en) 2019-10-08 2020-10-08 Aluminum alloy material

Publications (2)

Publication Number Publication Date
EP4043602A1 true EP4043602A1 (en) 2022-08-17
EP4043602A4 EP4043602A4 (en) 2023-11-01

Family

ID=75379714

Family Applications (1)

Application Number Title Priority Date Filing Date
EP20874847.5A Pending EP4043602A4 (en) 2019-10-08 2020-10-08 Aluminum alloy material

Country Status (7)

Country Link
US (1) US20220127701A1 (en)
EP (1) EP4043602A4 (en)
JP (1) JP7414452B2 (en)
KR (1) KR20220079494A (en)
CN (2) CN117802367A (en)
TW (1) TW202120708A (en)
WO (1) WO2021070889A1 (en)

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2841512A (en) * 1956-10-12 1958-07-01 William F Jobbins Inc Method of working and heat treating aluminum-magnesium alloys and product thereof
US3346371A (en) * 1965-05-20 1967-10-10 Olin Mathieson Aluminum base alloy
JPS5386610A (en) * 1977-01-10 1978-07-31 Kubota Ltd Aluminum alloy for casting
JPH07197170A (en) 1992-08-24 1995-08-01 Kobe Steel Ltd Aluminum alloy sheet for thin disk and its production
JP3098637B2 (en) * 1992-11-13 2000-10-16 川崎製鉄株式会社 Aluminum alloy sheet for high speed forming and method for producing the same
JP4164206B2 (en) 1999-09-28 2008-10-15 株式会社神戸製鋼所 High-strength, high-formability aluminum alloy sheet with excellent recrystallization grain refinement during high-temperature annealing
JP4224463B2 (en) * 2005-01-19 2009-02-12 株式会社神戸製鋼所 Aluminum alloy sheet for forming
JP4550598B2 (en) 2005-01-21 2010-09-22 株式会社神戸製鋼所 Aluminum alloy sheet for forming
JP2006316332A (en) * 2005-05-16 2006-11-24 Sumitomo Light Metal Ind Ltd Aluminum alloy sheet material having excellent drawing formability, and method for producing the same
JP4996853B2 (en) 2006-01-12 2012-08-08 古河スカイ株式会社 Aluminum alloy material for high temperature and high speed forming, method for manufacturing the same, and method for manufacturing aluminum alloy formed product
JP5354954B2 (en) * 2007-06-11 2013-11-27 住友軽金属工業株式会社 Aluminum alloy plate for press forming
JP5059505B2 (en) 2007-07-19 2012-10-24 株式会社神戸製鋼所 Aluminum alloy cold-rolled sheet that can be formed with high strength
JP5581254B2 (en) * 2010-03-31 2014-08-27 株式会社神戸製鋼所 Aluminum alloy plate for tab and manufacturing method thereof
US20140322558A1 (en) * 2011-11-02 2014-10-30 Uacj Corporation Aluminum alloy clad material for forming
JP6010454B2 (en) 2012-12-27 2016-10-19 住友電気工業株式会社 Aluminum alloy wire
CN105734364A (en) * 2016-03-25 2016-07-06 广州市华峰有色金属有限公司 High-end aluminum alloy material JH9 and preparation method thereof
JP6900199B2 (en) * 2017-02-10 2021-07-07 エス・エス・アルミ株式会社 Manufacturing method of aluminum alloy for casting, aluminum alloy casting products and aluminum alloy casting products
CN109097710B (en) * 2018-08-17 2020-05-19 清华大学 Extrusion method of high-magnesium aluminum alloy pipe

Also Published As

Publication number Publication date
JP7414452B2 (en) 2024-01-16
CN113661264A (en) 2021-11-16
KR20220079494A (en) 2022-06-13
CN113661264B (en) 2024-02-27
CN117802367A (en) 2024-04-02
JP2021059762A (en) 2021-04-15
EP4043602A4 (en) 2023-11-01
US20220127701A1 (en) 2022-04-28
WO2021070889A1 (en) 2021-04-15
TW202120708A (en) 2021-06-01

Similar Documents

Publication Publication Date Title
KR101331339B1 (en) Cu-ni-si-co based copper ally for electronic materials and manufacturing method therefor
EP3115474B1 (en) Structural aluminum alloy plate and process for producing same
JP4191159B2 (en) Titanium copper with excellent press workability
EP2915891B1 (en) Cu-be alloy and method for producing same
JP4025632B2 (en) Copper alloy
WO2012132765A1 (en) Cu-si-co-base copper alloy for electronic materials and method for producing same
EP4043601A1 (en) Aluminum alloy material
US20220389557A1 (en) Aluminum alloy precision plates
JPWO2015155911A1 (en) High-strength aluminum alloy plate excellent in bending workability and shape freezing property and method for producing the same
JP2020066756A (en) Titanium copper, manufacturing method of titanium copper, and electronic component
JP5718021B2 (en) Titanium copper for electronic parts
JP5628712B2 (en) Titanium copper for electronic parts
EP4043602A1 (en) Aluminum alloy material
EP3486340B1 (en) Aluminum alloy plastic working material and production method therefor
JP2004176162A (en) Copper alloy and manufacturing method therefor
EP3205734B1 (en) Superplastic-forming aluminium alloy plate and production method therefor
JP3843021B2 (en) Method for producing thick-walled Al-Mg alloy rolled sheet tempered material excellent in bending workability
JP7318275B2 (en) Al-Mg-Si-based aluminum alloy cold-rolled sheet and its manufacturing method, and Al-Mg-Si-based aluminum alloy cold-rolled sheet for forming and its manufacturing method
EP3561096B1 (en) Magnesium alloy plate and method for manufacturing same
JP4393031B2 (en) Method for producing Al-Mg alloy rolled sheet tempered material excellent in bending workability

Legal Events

Date Code Title Description
STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE INTERNATIONAL PUBLICATION HAS BEEN MADE

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

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

Free format text: STATUS: REQUEST FOR EXAMINATION WAS MADE

17P Request for examination filed

Effective date: 20210917

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

DAV Request for validation of the european patent (deleted)
DAX Request for extension of the european patent (deleted)
RAP1 Party data changed (applicant data changed or rights of an application transferred)

Owner name: UACJ CORPORATION

P01 Opt-out of the competence of the unified patent court (upc) registered

Effective date: 20230816

A4 Supplementary search report drawn up and despatched

Effective date: 20230928

RIC1 Information provided on ipc code assigned before grant

Ipc: C22F 1/047 20060101ALI20230922BHEP

Ipc: C22C 21/06 20060101AFI20230922BHEP