EP1702995A1 - METHOD FOR PRODUCING Al-Mg-Si ALLOY EXCELLENT IN BAKE-HARDENABILITY AND HEMMABILITY - Google Patents

METHOD FOR PRODUCING Al-Mg-Si ALLOY EXCELLENT IN BAKE-HARDENABILITY AND HEMMABILITY Download PDF

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Publication number
EP1702995A1
EP1702995A1 EP04806942A EP04806942A EP1702995A1 EP 1702995 A1 EP1702995 A1 EP 1702995A1 EP 04806942 A EP04806942 A EP 04806942A EP 04806942 A EP04806942 A EP 04806942A EP 1702995 A1 EP1702995 A1 EP 1702995A1
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EP
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Prior art keywords
cooling
treatment
less
cooling rate
temperature
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Application number
EP04806942A
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German (de)
French (fr)
Inventor
Pizhi; c/o Nippon Light Metal Company Ltd. ZHAO
T.; c/o Nippon Light Metal Company Ltd. ANAMI
T.; c/o Nippon Light Metal Company Ltd KOBAYASHI
I.; c/o Nippon Light Metal Company Ltd. OKAMOTO
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Nippon Light Metal Co Ltd
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Nippon Light Metal Co Ltd
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Publication of EP1702995A1 publication Critical patent/EP1702995A1/en
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    • 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
    • C22F1/05Changing 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 of the Al-Si-Mg type, i.e. containing silicon and magnesium in approximately equal proportions
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D11/00Continuous casting of metals, i.e. casting in indefinite lengths
    • B22D11/06Continuous casting of metals, i.e. casting in indefinite lengths into moulds with travelling walls, e.g. with rolls, plates, belts, caterpillars
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D11/00Continuous casting of metals, i.e. casting in indefinite lengths
    • B22D11/06Continuous casting of metals, i.e. casting in indefinite lengths into moulds with travelling walls, e.g. with rolls, plates, belts, caterpillars
    • B22D11/0605Continuous casting of metals, i.e. casting in indefinite lengths into moulds with travelling walls, e.g. with rolls, plates, belts, caterpillars formed by two belts, e.g. Hazelett-process
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B22CASTING; POWDER METALLURGY
    • B22DCASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
    • B22D11/00Continuous casting of metals, i.e. casting in indefinite lengths
    • B22D11/12Accessories for subsequent treating or working cast stock in situ
    • B22D11/124Accessories for subsequent treating or working cast stock in situ for cooling
    • 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
    • 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

Definitions

  • the present invention relates to a production method for obtaining an Al-Mg-Si alloy sheet that is abundant in hemmability while simultaneously having a high age-hardening ability, by casting a thin slab by continuous casting of an Al-Mg-Si alloy, performing a homogenization treatment, then cold rolling, and performing a solution treatment in a continuous annealing furnace as needed.
  • the present method it is possible to produce, at a low cost as compared to the conventional art, rolled sheets of Al-Mg-Si alloy that are suitable for forming by bending, press forming and the like of automotive parts, household appliances and the like.
  • Al-Mg-Si alloys have the property of increasing in strength when heat is applied during processes such as coating after forming, so that they are well-suited for use in automotive panels or the like. Furthermore, the production of sheets of the alloys by continuous casting and rolling has been proposed to reduce costs by improved productivity.
  • Japanese Patent Application, First Publication No. S62-207851 discloses an aluminum alloy sheet for forming and method of production thereof, obtained by continuous casting of an aluminum alloy melt comprising 0.4-2.5% Si, 0.1-1.2% Mg and one or more among 1.5% or less of Cu, 2.5% or less of Zn, 0.3% or less of Cr, 0.6% or less of Mn and 0.3% or less of Zr, to form a 3-15 mm thick slab, cold rolling, then performing a solution treatment and quenching, characterized in that the maximum size of intermetallic compounds in the matrix is 5 ⁇ m or less.
  • Japanese Patent Application, First Publication No. H10-110232 discloses an Al-Mg-Si alloy sheet, obtained by preparing a direct cast rolled sheet of Al alloy comprising 0.2-3.0% Si and 0.2-3.0% Mg, containing one or more of 0.01-0.5% Mn, 0.01-0.5% Cr, 0.01-0.5% Zr and 0.001-0.5% Ti, and further containing 0-2.5% Cu, 0-0.2% Sn and 0-2.0% Zn, with Fe being limited to 1.0% or less and the remainder consisting of Al and unavoidable impurities, and further cold rolling, characterized in that the maximum crystal size in the metallic portion of the sheet is 100 ⁇ m or less and the maximum length of continuous Mg 2 Si compounds on the surface layer portion is 50 ⁇ m or less.
  • Japanese Patent Application, First Publication No. 2001-262264 proposes an Al-Mg-Si alloy sheet excelling in ductility and bendability, the aluminum alloy comprising 0.1-2.0% Si, 0.1-2.0% Mg, 0.1-1.5% Fe or one or more further elements chosen from among 2% or less of Cu, 0.3% or less of Cr, 1.0% or less of Mn, 0.3% or less of Zr, 0.3% or less of V, 0.03% or less of Ti, 1.5% or less of Zn and 0.2% or less of Ag, wherein the maximum size of intermetallic compounds is 5 ⁇ m or less, the maximum aspect ratio is 5 or less and the average crystal grain size is 30 ⁇ m or less.
  • Alloy sheets that are used as outer panels in automotive body sheets or the like require exceptional hemmability and bake-hardenability. For this reason, Al-Mg-Si alloy sheets that excel in bendability and age-harden when heated have been sought. However, sheets produced by continuous casting and rolling have the drawbacks of poor hemmability and insufficient bake-hardenability after coating.
  • the problem to be solved by the present invention is to obtain, at a low cost, an Al-Mg-Si alloy sheet for forming that suppresses GP zones that are deposited during natural ageing when left at room temperature, achieves a high level of bake-hardening due to a reinforcement phase being quickly deposited upon heating during coating and baking, while simultaneously having abundant bendability.
  • a thin slab of Al-Mg-Si alloy is continuously cast by a twin-belt casting machine, the cast thin slab is directly wound, subjected to a homogenization treatment under appropriate conditions, and cold rolled, then combined with a solution treatment in a continuous annealing furnace as needed, thereby fragmenting the compounds and raising the hemmability while simultaneously enabling the procedure to be considerably shortened. Furthermore, microsegregation is reduced by a homogenization treatment, and the cooling rate after the homogenization treatment is raised, thereby reducing the deposition of Mg 2 Si while cooling, to obtain an aluminum sheet for automotive body sheets with excellent bake-hardenabiltiy and hemmability after a final anneal.
  • the present invention which solves the above problem relates to a method of producing aluminum alloy sheets characterized by winding into thin slabs, subjecting to a homogenization treatment, cold rolling, then subjecting to a solution treatment.
  • a method of producing aluminum alloy sheets excelling in bake-hardenability and hemmability comprising steps of casting, by means of a twin-belt casting method, an alloy melt comprising 0.30-1.00 wt% of Mg, 0.30-1.20 wt% of Si, 0.05-0.50 wt% of Fe, 0.05-0.50 wt% of Mn and 0.005-0.10 wt% of Ti, optionally further comprising at least one of 0.05-0.70 wt% of Cu or 0.05-0.40 wt% of Zr, the remainder consisting of Al and unavoidable impurities, to form a 5-15 mm thick slab at a cooling rate of 40-150 °C/s at a quarter-thickness of the slab;
  • the homogenization treatment preferably involves heating to 520-580 °C at a heating rate of at least 30 °C/h in a batch furnace, then holding at that temperature for 2-24 hours (invention according to claim 2).
  • the solution treatment preferably involves heating to 530-560 °C at a heating rate of at least 10 °C/s in a continuous annealing line, and holding for 30 seconds or less (invention according to claim 3).
  • the solution treatment may be followed by steps of cooling to room temperature at a cooling rate of at least 10 °C/s, then subjecting to a restoration treatment by holding for 30 seconds or less at 260-300 °C in a continuous annealing furnace, and cooling to room temperature at a cooling rate of at least 10 °C/s (invention according to claim 4).
  • the solution treatment may be followed by steps of water-cooling to 250 °C or less at a cooling rate of at least 10 °C/s, then air-cooling to 60-100 °C at a cooling rate of 1-20 °C/s, coiling up, and subjecting to a preliminary ageing treatment by cooling to room temperature (invention according to claim 5).
  • the solution treatment may be followed by steps of cooling to room temperature at a cooling rate of at least 10 °C/s, then subjecting to a restoration treatment by holding for 30 seconds or less at 260-300 °C in a continuous annealing furnace, cooling to 60-100 °C at a cooling rate of at least 1 °C/s, coiling up, and subjecting to a preliminary ageing treatment by cooling to room temperature (invention according to claim 6).
  • the aluminum alloy sheet production method of the present invention it is possible to obtain an aluminum alloy sheet with exceptional hemmability and bake-hardenability. Additionally, this production method is capable of obtaining an aluminum alloy sheet in an extremely short procedure and at low cost.
  • the present invention relates to a method of producing a rolled sheet of AI-Mg-Si alloy, characterized by casting a thin slab by a twin-belt casting method, winding the slab directly onto a coil, subjecting to a homogenization treatment, then cold rolling, and further subjecting to a solution treatment.
  • an alloy melt consisting of the aforementioned composition is cast into a slab 5-15 mm thick at a cooling rate of 40-150 °C/s at a quarter thickness of the slab, using a twin-belt casting method, and after winding into a coil, it is subjected to a homogenization treatment and cooled to 250 °C or less at a cooling rate of at least 500 °C/s, then cold rolled, and subsequently subjected to a solution treatment.
  • the twin-belt casting method is a method of casting thin slabs by pouring a melt between water-cooled rotating belts that oppose each other from above and below, so as to harden the melt by cooling through the belt surfaces.
  • slabs that are 5-15 mm thick are cast by the twin-belt casting method. If the slab thickness exceeds 15 mm, it becomes difficult to wind the thin slabs into coils, and if the slab thickness is less than 5 mm, there is a loss in productivity and it becomes difficult to cast the thin slabs.
  • the cooling rate 40-150 °C/s at a quarter thickness of the slab.
  • the cooling rate is computed by measuring the DAS (Dendrite Arm Spacing) by a line intersection method from observations of the microstructure in the slab at quarter thickness.
  • the cooling rate is less than 40 °C/s, the cast structure formed in the central portion of the slab during hardening becomes coarse, thus reducing the hemmability, while if the cooling rate exceeds 150 °C/s, Al-Fe-Si crystals and Al-(Fe ⁇ Mn)-Si crystals become 1 ⁇ m or less and the size of recrystallized grains becomes coarse at 30 ⁇ m or more.
  • this coil After winding a thin slab, this coil is subjected to a homogenization treatment under appropriate conditions to fragment the Al-Fe-Si crystals and Al-(Fe ⁇ Mn)-Si crystals that have an adverse effect on hemmability, thus improving the hemmability. Furthermore, it is possible to obtain thin slabs in a state where relatively small Mg 2 Si crystals that reside in the cast structure are completely dissolved into the matrix, thus raising the effectiveness of the solid solution treatment after the cold rolling process.
  • the reason that the cooling after the homogenization treatment is performed at a rate of at least 500 °C/s and to 250 °C or less is in order to suppress the deposition of relatively coarse Mg 2 Si as much as possible, and to dissolve the Mg and Si into the matrix in an oversaturated state.
  • the coil After winding the thin slab, the coil is inserted into a batch furnace, and heated at a rate of at least 30 °C/h to 520-580 °C, at which temperature it is held for 2-24 hours to perform a homogenization treatment, after which the coil may be extracted from the batch furnace and forcibly air-cooled to room temperature at a cooling rate of at least 500 °C/h.
  • This cooling can be performed, for example, by a fan while unwinding the coil.
  • the reason the heating rate to the homogenization temperature is limited to at least 30 °C/h for the homogenization treatment following winding of the thin slab is that if the heating rate is less than 30 °C/h, at least 16 hours will be required to reach the predetermined homogenization temperature, thus raising costs.
  • the reason the homogenization temperature is within the range of 520-580 °C is that if the temperature is less than 520 °C, the fragmentation of Al-Fe-Si crystals and Al-(Fe ⁇ Mn)-Si crystals is inadequate, and not enough to dissolve the Mg 2 Si that crystallized during casting into the matrix, and if the temperature exceeds 580 °C, the metals with low melting points will melt and cause burning.
  • the reason that the homogenization treatment time is set to within the range of 2-24 hours is because if the treatment time is less than 2 hours, the fragmentation of Al-Fe-Si crystals and Al-(Fe ⁇ Mn)-Si crystals is inadequate, and not enough to dissolve the Mg 2 Si that crystallized during casting into the matrix, and if the treatment time exceeds 24 hours, the Mg 2 Si that crystallized during casting is well-dissolved into the matrix, and the Mg and Si become saturated, resulting in cost increases.
  • the invention is characterized by further cold rolling this coil and performing a solution treatment.
  • This solution treatment is preferably performed in a normal continuous annealing line (CAL).
  • CAL normal continuous annealing line
  • a continuous annealing line is an installation for performing continuous solution treatments and the like of coils, characterized by comprising inductive heating devices for performing heat treatments, water tanks for water-cooling, air nozzles for air-cooling, and the like.
  • the solution treatment it should preferably be performed by heating at a rate of at least 10 °C/s to 530-560 °C by means of a continuous annealing line, and holding for 30 seconds or less.
  • the reason the heating rate to the solution treatment temperature is limited to at least 10 °C/s in the solution treatment is that if the heating rate is less than 10 °C/s, the coil advancing speed becomes too slow, as a result of which the processing time becomes long and the cost mounts.
  • the reason the solution treatment temperature is set to be within the range of 530-560 °C is that if the temperature is less than 530 °C, it is not sufficient to cause Mg 2 Si that crystallized while casting or precipitated while being cooled after homogenization to be dissolved into the matrix, and if the temperature exceeds 560 °C, the metals with low melting points will melt and cause burning.
  • the reason the solution treatment time is restricted to be within 30 seconds is that in the case of treatment times exceeding 30 seconds, Mg 2 Si that crystallized while casting or precipitated while being cooled after homogenization is well-dissolved into the matrix, and the Mg and Si become saturated, thereby slowing the coil advancement speed, as a result of which the processing time is increased and the costs mount.
  • the invention is characterized by cooling to room temperature at a rate of at least 10 °C/s after the solution treatment.
  • the reason the cooling rate after the solution treatment is at least 10 °C/s is that if the cooling rate is less than 10 °C/s, Si is deposited in the crystal grain boundary during the cooling step, thus reducing the hemmability.
  • the thin slab After performing the aforementioned homogenization treatment on the thin slab, it is further cold rolled, subjected to a solution treatment and cooled to room temperature at a rate of at least 10 °C/s, and after the coil is left at room temperature, it may be held for 30 seconds or less at 260-300 °C in a continuous annealing line, then cooled to room temperature at 10 °C/s.
  • a continuous annealing line is an installation for performing continuous solution treatments and the like of coils, characterized by comprising inductive heating devices for performing heat treatments, water tanks for water-cooling, air nozzles for air-cooling, and the like. Due to the restoration treatment, it is possible to re-dissolve GP zones that appear due to natural ageing when left at room temperature after a solution treatment, thus enabling adequate strength to be obtained after heating for coating and baking.
  • the reason the time over which the restoration treatment temperature is held is restricted to within 30 seconds is that if the treatment time exceeds 30 seconds, it is not possible to adequately re-dissolve the GP zones that appear due to natural ageing when left at room temperature after the solution treatment, in addition to which the coil advancement speed is too slow, as a result of which the treatment time is long and the costs mount.
  • the thin slab After performing the aforementioned homogenization treatment on the thin slab, it can be further cold rolled, subjected to a heat solution treatment in a continuous annealing line, water-cooled to 250 °C or less at a cooling rate (first cooling rate) of at least 10 °C/s, then air-cooled to 60-100 °C at a cooling rate (second cooling rate) of 1-20 °C/s, coiled up and cooled to room temperature.
  • first cooling rate water-cooled to 250 °C or less at a cooling rate (first cooling rate) of at least 10 °C/s
  • second cooling rate a cooling rate of 1-20 °C/s
  • This heat solution treatment and subsequent cooling are preferably performed in a normal continuous annealing line (CAL).
  • CAL normal continuous annealing line
  • the thin slab After subjecting the thin slab to a homogenization treatment and further cold rolling, it may be subjected to a solution treatment by heating to 530-560 °C at a rate of at least 10 °C/s, then holding for 30 seconds or less, then cooled to room temperature at a rate of at least 10 °C/s, thereafter subjected to a restoration treatment by holding within a range of 260-300 °C for 30 seconds, then cooled to 60-100 °C at a cooling rate of at least 1 °C/s, coiled up and subjected to a preliminary ageing treatment by cooling to room temperature.
  • a solution treatment by heating to 530-560 °C at a rate of at least 10 °C/s, then holding for 30 seconds or less, then cooled to room temperature at a rate of at least 10 °C/s, thereafter subjected to a restoration treatment by holding within a range of 260-300 °C for 30 seconds, then cooled to 60-100 °C at
  • This solution treatment and subsequent cooling, and restoration treatment and subsequent cooling are preferably performed in a normal continuous annealing line (CAL).
  • CAL normal continuous annealing line
  • the essential element Mg is dissolved in the matrix after the heat solution treatment, and is deposited as a reinforcing phase together with Si upon heating for coating and baking, thereby improving the strength.
  • the reason the Mg content is limited to 0.30-1.00 wt% is that the effect is small if less than 0.30 wt%, and if more than 1.00 wt%, the hemmability after the solution treatment is reduced.
  • a more preferable range for the Mg content is 0.30-0.70 wt%.
  • the essential element Si is deposited together with Mg as an intermediary phase of Mg 2 Si known as ⁇ " or an analogous reinforcing phase upon being heated for coating and baking, thereby increasing the strength.
  • the reason the Si content is limited to 0.30-1.20 wt% is that if less than 0.30 wt%, its effects are minimal, and if more than 1.20 wt%, the hemmability is reduced after the heat solution treatment.
  • a more preferable range of Si content is 0.60-1.20 wt%.
  • the essential element Fe when coexisting with Si and Mn, generates many Al-Fe-Si crystals and Al-(Fe ⁇ Mn)-Si crystals of a size of 5 ⁇ m or less upon casting, so that re-crystallized nuclei are increased, as a result of which the recrystallized grains are refined and sheets of exceptional formability are obtained. If the Fe content is less than 0.05 wt%, the effects are not very remarkable.
  • the preferable range of Fe content is 0.05-0.50 wt%.
  • a more preferable range of Fe content is 0.05-0.30 wt%.
  • the essential element Mn is added as an element to refine the re-crystallized grains.
  • the size of the re-crystallized grains By keeping the size of the re-crystallized grains relatively small at 10-25 ⁇ m, it is possible to form sheets with exceptional formability. If the Mn content is less than 0.05 wt%, the effect is not adequate, and if it exceeds 0.50 wt%, coarse Al-Fe-Si crystals and Al-(Fe ⁇ Mn)-Si crystals are formed upon casting, thus not only reducing the hemmability but also reducing the amount of Si dissolved in the thin slabs, as a result of which the bake-hardenability of the final sheets is reduced. Therefore, the preferable range of Mn content is 0.05-0.50 wt%. A more preferable range of Mn content is 0.05-0.30 wt%.
  • the essential element Ti will not inhibit the effects of the present invention if it is contained at 0.10 wt% or less, and it can function as a crystal grain refiner for the thin slabs, so as to reliably prevent casting defects of the slabs such as cracks or the like. If the Ti content is less than 0.005 wt%, the effects are not adequate, and if the Ti content exceeds 0.10 wt%, coarse intermetallic compounds such as TiAl 3 and the like are formed during casting, thus greatly reducing the hemmability. Therefore, the preferable range of Ti content is 0.005-0.10 wt%. A more preferable range for the Ti content is 0.005-0.05 wt%.
  • the optional element Cu is an element that promotes age-hardening and raises the bake-hardenability. If the Cu content is less than 0.05 wt%, the effect is small, and if it exceeds 0.70 wt%, the yield strength of the sheets becomes high after a preliminary ageing treatment, and not only does the hemmability decrease, but the reduction in corrosion resistance is also marked. Therefore, the Cu content is preferably within a range of 0.05-0.70 wt%. The Cu content is more preferably 0.10-0.60 wt%.
  • the optional element Zr is added as an element for refining the re-crystallized grains. If the Zr content is less than 0.05 wt%, the effect is not adequate, and if it exceeds 0.40 wt%, coarse Al-Zr crystals are created during slab casting, thus reducing the hemmability. Therefore, the Zr content is preferably within a range of 0.05-0.40 wt%. The Zr content is more preferably within a range of 0.05-0.30 wt%.
  • the present invention allows an Al-Mg-Si alloy sheet for use in automotive body sheets having exceptional bake-hardenablitiy and hemmability after a final anneal to be produced at low cost. While a restoration treatment or high-temperature winding is required to suppress natural ageing as with conventional methods, the steps such as facing, hot rolling and the like that precede these steps can be largely simplified, thus greatly reducing the total production cost.
  • the samples after cold rolling are not coils but all cut sheets. Therefore, in order to simulate the step of continuous annealing of a coil in a continuous annealing line (CAL), a solution treatment of the samples in a salt bath and a cold water quench or 85 °C water quench were employed.
  • CAL continuous annealing line
  • solution treatments were performed on these cold rolled sheets in a salt bath, and they were either 1) quenched in 85 °C water and immediately inserted into an annealer with a predetermined atmospheric temperature to perform a heat treatment under predetermined conditions, or 2) quenched in cold water, left at room temperature for 24 hours, then subjected to a heat treatment under predetermined conditions. Furthermore, in order to simulate automobile coating steps, they were held for one week at room temperature after the heat treatment, and measured for 0.2% yield strength, further baked at 180 °C for 30 minutes, and again measured for 0.2% yield strength.
  • Table 2 shows the results for cases in which the homogenization conditions and cooling rate after the homogenization treatment were changed.
  • the slabs were cold rolled to a thickness of 1 mm, these cold rolled sheets were subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, then quenched with 85 °C water, and immediately inserted into an annealer with an atmospheric temperature of 85 °C to perform a preliminary ageing of 8 hours.
  • Those falling within the scope of conditions of the present invention (1-7) had exceptional bake-hardenability and hemmability.
  • Those that did not undergo a homogenization treatment (8, 10) had poor bake-hardenability and hemmability.
  • those which had a slow cooling rate after the homogenization treatment had poor bake-hardenability (9).
  • Table 3 shows the results when the temperatures/times of the homogenization treatment are changed.
  • the slabs were cold rolled to a thickness of 1 mm, these cold rolled sheets were subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, then quenched in 85 °C water and immediately entered into an annealer with an atmospheric temperature of 85 °C to perform a preliminary ageing of 8 hours.
  • Those falling within the scope of conditions of the present invention (11-14) had exceptional bake-hardenability and hemmability.
  • Table 4 shows the results when the homogenization conditions and restoration conditions were changed.
  • the slabs were cold rolled to a thickness of 1 mm, these cold rolled sheets are subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, then quenched in cold water, and after leaving at room temperature for 24 hours, subjected to a restoration treatment by holding for 15 seconds at a predetermined temperature.
  • Those falling within the scope of conditions of the present invention (17-20) had exceptional bake-hardenability and hemmability.
  • Those that had a low restoration temperature (reheating temperature) (21) had poor bake-hardenability.
  • Table 5 shows the results when the homogenization conditions and cooling pattern after the solution treatment were changed.
  • the cooling rate after the solution treatment was divided into two stages, with the cooling rate from the solution temperature to an intermediate temperature being defined as the first cooling rate and the cooling rate from the intermediate temperature to the coil-up temperature being defined as the second cooling rate.
  • the slabs were cold rolled to a thickness of 1 mm, and these cold rolled sheets were subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, after which they were cooled to the intermediate temperature at the first cooling rate, then cooled to the coil-up temperature at the second cooling rate, and thereafter cooled to room temperature at 5 °C/h.
  • Table 6 shows the results when the restoration treatment temperature (reheating temperature) after the solution treatment and coil-up temperature were changed.
  • the slabs were cold rolled to a thickness of 1 mm, these cold rolled sheets are subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, then quenched in cold water, and after leaving at room temperature for 24 hours, held for 15 seconds at a predetermined temperature (preheating temperature) and cooled to a predetermined coil-up temperature at 10 °C/s, then further cooled to room temperature at 10 °C/h.
  • preheating temperature a predetermined temperature
  • Example 41 B 550 320 85 124/234 110 X 42 B 550 250 80 111/198 87 ⁇ 43 B 550 260 40 110/185 75 ⁇ 44 B 550 290 120 131/249 118 X Homogenization: 550 °C ⁇ 6 h Cooling Rate after Homogenization: 1000 °C/h
  • rolled sheets of Al-Mg-Si alloy that are suitable for forming by bending, press forming and the like of automotive parts, household appliances and the like can be produced at a low cost relative to the conventional art.

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Abstract

[PROBLEMS] To provide a method for producing an aluminum alloy sheet excellent in bake-hardenability and hemmability at a low cost by the employment of a very short production process.
[MEANS FOR SOLVING PROBLEMS] A method for producing an aluminum alloy sheet, which comprises providing an aluminum alloy melt having a chemical composition, in wt%, that Mg: 0.30 to 1.00 %, Si: 0.30 to 1.20 %, Fe: 0.05 to 0.50 %, Mn: 0.05 to 0.50 %, Ti: 0.005 to 0.10 %, optionally further one or more of Cu: R0.05 to 0.70 % and Zr: 0.05 to 0.40 %, and the balance: Al and inevitable impurities, casting the alloy melt into a slab having a thickness of 5 to 15 mm by the twin belt casting method with a cooling speed at 1/4 of the thickness of the slab of 40 to 150 °C/s, winding up a coil, subjecting the coil to a homogenizing treatment, cooling the resultant coil to a temperature of 250 °C or lower with a cooling speed of 500 °C/hr or more, followed by cold rolling, and then subjecting the resulting product to a solution treatment.

Description

    TECHNICAL FIELD
  • The present invention relates to a production method for obtaining an Al-Mg-Si alloy sheet that is abundant in hemmability while simultaneously having a high age-hardening ability, by casting a thin slab by continuous casting of an Al-Mg-Si alloy, performing a homogenization treatment, then cold rolling, and performing a solution treatment in a continuous annealing furnace as needed. According to the present method, it is possible to produce, at a low cost as compared to the conventional art, rolled sheets of Al-Mg-Si alloy that are suitable for forming by bending, press forming and the like of automotive parts, household appliances and the like.
  • BACKGROUND ART
  • Al-Mg-Si alloys have the property of increasing in strength when heat is applied during processes such as coating after forming, so that they are well-suited for use in automotive panels or the like. Furthermore, the production of sheets of the alloys by continuous casting and rolling has been proposed to reduce costs by improved productivity.
  • For example, Japanese Patent Application, First Publication No. S62-207851 discloses an aluminum alloy sheet for forming and method of production thereof, obtained by continuous casting of an aluminum alloy melt comprising 0.4-2.5% Si, 0.1-1.2% Mg and one or more among 1.5% or less of Cu, 2.5% or less of Zn, 0.3% or less of Cr, 0.6% or less of Mn and 0.3% or less of Zr, to form a 3-15 mm thick slab, cold rolling, then performing a solution treatment and quenching, characterized in that the maximum size of intermetallic compounds in the matrix is 5 µm or less.
  • Japanese Patent Application, First Publication No. H10-110232 discloses an Al-Mg-Si alloy sheet, obtained by preparing a direct cast rolled sheet of Al alloy comprising 0.2-3.0% Si and 0.2-3.0% Mg, containing one or more of 0.01-0.5% Mn, 0.01-0.5% Cr, 0.01-0.5% Zr and 0.001-0.5% Ti, and further containing 0-2.5% Cu, 0-0.2% Sn and 0-2.0% Zn, with Fe being limited to 1.0% or less and the remainder consisting of Al and unavoidable impurities, and further cold rolling, characterized in that the maximum crystal size in the metallic portion of the sheet is 100 µm or less and the maximum length of continuous Mg2Si compounds on the surface layer portion is 50 µm or less.
  • Additionally, Japanese Patent Application, First Publication No. 2001-262264 proposes an Al-Mg-Si alloy sheet excelling in ductility and bendability, the aluminum alloy comprising 0.1-2.0% Si, 0.1-2.0% Mg, 0.1-1.5% Fe or one or more further elements chosen from among 2% or less of Cu, 0.3% or less of Cr, 1.0% or less of Mn, 0.3% or less of Zr, 0.3% or less of V, 0.03% or less of Ti, 1.5% or less of Zn and 0.2% or less of Ag, wherein the maximum size of intermetallic compounds is 5 µm or less, the maximum aspect ratio is 5 or less and the average crystal grain size is 30 µm or less.
    • Patent Document 1: Japanese Patent Application, First Publication No. S62-207851
    • Patent Document 2: Japanese Patent Application, First Publication No. H10-110232
    • Patent Document 3: Japanese Patent Application, First Publication No. 2001-262264
    DISCLOSURE OF THE INVENTION Problems to be Solved by the Invention
  • Alloy sheets that are used as outer panels in automotive body sheets or the like require exceptional hemmability and bake-hardenability. For this reason, Al-Mg-Si alloy sheets that excel in bendability and age-harden when heated have been sought. However, sheets produced by continuous casting and rolling have the drawbacks of poor hemmability and insufficient bake-hardenability after coating.
  • The problem to be solved by the present invention is to obtain, at a low cost, an Al-Mg-Si alloy sheet for forming that suppresses GP zones that are deposited during natural ageing when left at room temperature, achieves a high level of bake-hardening due to a reinforcement phase being quickly deposited upon heating during coating and baking, while simultaneously having abundant bendability.
  • Means for Solving the Problems
  • A thin slab of Al-Mg-Si alloy is continuously cast by a twin-belt casting machine, the cast thin slab is directly wound, subjected to a homogenization treatment under appropriate conditions, and cold rolled, then combined with a solution treatment in a continuous annealing furnace as needed, thereby fragmenting the compounds and raising the hemmability while simultaneously enabling the procedure to be considerably shortened. Furthermore, microsegregation is reduced by a homogenization treatment, and the cooling rate after the homogenization treatment is raised, thereby reducing the deposition of Mg2Si while cooling, to obtain an aluminum sheet for automotive body sheets with excellent bake-hardenabiltiy and hemmability after a final anneal.
  • The present invention which solves the above problem relates to a method of producing aluminum alloy sheets characterized by winding into thin slabs, subjecting to a homogenization treatment, cold rolling, then subjecting to a solution treatment. Specifically, as recited in claim 1, it is a method of producing aluminum alloy sheets excelling in bake-hardenability and hemmability, comprising steps of casting, by means of a twin-belt casting method, an alloy melt comprising 0.30-1.00 wt% of Mg, 0.30-1.20 wt% of Si, 0.05-0.50 wt% of Fe, 0.05-0.50 wt% of Mn and 0.005-0.10 wt% of Ti, optionally further comprising at least one of 0.05-0.70 wt% of Cu or 0.05-0.40 wt% of Zr, the remainder consisting of Al and unavoidable impurities, to form a 5-15 mm thick slab at a cooling rate of 40-150 °C/s at a quarter-thickness of the slab; winding into a coil; subjecting to a homogenization treatment; cooling to 250 °C or less at a cooling rate of at least 500 °C/h; cold rolling; then subjecting to a solution treatment (invention according to claim 1).
  • In the above production method, the homogenization treatment preferably involves heating to 520-580 °C at a heating rate of at least 30 °C/h in a batch furnace, then holding at that temperature for 2-24 hours (invention according to claim 2).
  • The solution treatment preferably involves heating to 530-560 °C at a heating rate of at least 10 °C/s in a continuous annealing line, and holding for 30 seconds or less (invention according to claim 3).
  • Furthermore, in the invention according to claim 3 mentioned above, the solution treatment may be followed by steps of cooling to room temperature at a cooling rate of at least 10 °C/s, then subjecting to a restoration treatment by holding for 30 seconds or less at 260-300 °C in a continuous annealing furnace, and cooling to room temperature at a cooling rate of at least 10 °C/s (invention according to claim 4).
  • Alternatively, in the invention according to claim 3 mentioned above, the solution treatment may be followed by steps of water-cooling to 250 °C or less at a cooling rate of at least 10 °C/s, then air-cooling to 60-100 °C at a cooling rate of 1-20 °C/s, coiling up, and subjecting to a preliminary ageing treatment by cooling to room temperature (invention according to claim 5).
  • Alternatively, in the invention according to claim 3 mentioned above, the solution treatment may be followed by steps of cooling to room temperature at a cooling rate of at least 10 °C/s, then subjecting to a restoration treatment by holding for 30 seconds or less at 260-300 °C in a continuous annealing furnace, cooling to 60-100 °C at a cooling rate of at least 1 °C/s, coiling up, and subjecting to a preliminary ageing treatment by cooling to room temperature (invention according to claim 6).
  • Effects of the Invention
  • According to the aluminum alloy sheet production method of the present invention, it is possible to obtain an aluminum alloy sheet with exceptional hemmability and bake-hardenability. Additionally, this production method is capable of obtaining an aluminum alloy sheet in an extremely short procedure and at low cost.
  • BEST MODE FOR CARRYING OUT THE INVENTION
  • The present invention relates to a method of producing a rolled sheet of AI-Mg-Si alloy, characterized by casting a thin slab by a twin-belt casting method, winding the slab directly onto a coil, subjecting to a homogenization treatment, then cold rolling, and further subjecting to a solution treatment.
  • In the present invention, an alloy melt consisting of the aforementioned composition is cast into a slab 5-15 mm thick at a cooling rate of 40-150 °C/s at a quarter thickness of the slab, using a twin-belt casting method, and after winding into a coil, it is subjected to a homogenization treatment and cooled to 250 °C or less at a cooling rate of at least 500 °C/s, then cold rolled, and subsequently subjected to a solution treatment.
  • The twin-belt casting method is a method of casting thin slabs by pouring a melt between water-cooled rotating belts that oppose each other from above and below, so as to harden the melt by cooling through the belt surfaces. In the present invention, slabs that are 5-15 mm thick are cast by the twin-belt casting method. If the slab thickness exceeds 15 mm, it becomes difficult to wind the thin slabs into coils, and if the slab thickness is less than 5 mm, there is a loss in productivity and it becomes difficult to cast the thin slabs.
  • By casting a slab 5-15 mm thick using the twin-belt casting method, it is possible to make the cooling rate 40-150 °C/s at a quarter thickness of the slab. The cooling rate is computed by measuring the DAS (Dendrite Arm Spacing) by a line intersection method from observations of the microstructure in the slab at quarter thickness. When the cooling rate is less than 40 °C/s, the cast structure formed in the central portion of the slab during hardening becomes coarse, thus reducing the hemmability, while if the cooling rate exceeds 150 °C/s, Al-Fe-Si crystals and Al-(Fe·Mn)-Si crystals become 1 µm or less and the size of recrystallized grains becomes coarse at 30 µm or more.
  • After winding a thin slab, this coil is subjected to a homogenization treatment under appropriate conditions to fragment the Al-Fe-Si crystals and Al-(Fe·Mn)-Si crystals that have an adverse effect on hemmability, thus improving the hemmability. Furthermore, it is possible to obtain thin slabs in a state where relatively small Mg2Si crystals that reside in the cast structure are completely dissolved into the matrix, thus raising the effectiveness of the solid solution treatment after the cold rolling process.
  • The reason that the cooling after the homogenization treatment is performed at a rate of at least 500 °C/s and to 250 °C or less is in order to suppress the deposition of relatively coarse Mg2Si as much as possible, and to dissolve the Mg and Si into the matrix in an oversaturated state.
  • After winding the thin slab, the coil is inserted into a batch furnace, and heated at a rate of at least 30 °C/h to 520-580 °C, at which temperature it is held for 2-24 hours to perform a homogenization treatment, after which the coil may be extracted from the batch furnace and forcibly air-cooled to room temperature at a cooling rate of at least 500 °C/h. This cooling can be performed, for example, by a fan while unwinding the coil.
  • The reason the heating rate to the homogenization temperature is limited to at least 30 °C/h for the homogenization treatment following winding of the thin slab is that if the heating rate is less than 30 °C/h, at least 16 hours will be required to reach the predetermined homogenization temperature, thus raising costs.
  • The reason the homogenization temperature is within the range of 520-580 °C is that if the temperature is less than 520 °C, the fragmentation of Al-Fe-Si crystals and Al-(Fe·Mn)-Si crystals is inadequate, and not enough to dissolve the Mg2Si that crystallized during casting into the matrix, and if the temperature exceeds 580 °C, the metals with low melting points will melt and cause burning.
  • Additionally, the reason that the homogenization treatment time is set to within the range of 2-24 hours is because if the treatment time is less than 2 hours, the fragmentation of Al-Fe-Si crystals and Al-(Fe·Mn)-Si crystals is inadequate, and not enough to dissolve the Mg2Si that crystallized during casting into the matrix, and if the treatment time exceeds 24 hours, the Mg2Si that crystallized during casting is well-dissolved into the matrix, and the Mg and Si become saturated, resulting in cost increases.
  • The invention is characterized by further cold rolling this coil and performing a solution treatment. This solution treatment is preferably performed in a normal continuous annealing line (CAL).
  • A continuous annealing line (CAL) is an installation for performing continuous solution treatments and the like of coils, characterized by comprising inductive heating devices for performing heat treatments, water tanks for water-cooling, air nozzles for air-cooling, and the like.
  • As for the solution treatment, it should preferably be performed by heating at a rate of at least 10 °C/s to 530-560 °C by means of a continuous annealing line, and holding for 30 seconds or less.
  • The reason the heating rate to the solution treatment temperature is limited to at least 10 °C/s in the solution treatment is that if the heating rate is less than 10 °C/s, the coil advancing speed becomes too slow, as a result of which the processing time becomes long and the cost mounts.
  • The reason the solution treatment temperature is set to be within the range of 530-560 °C is that if the temperature is less than 530 °C, it is not sufficient to cause Mg2Si that crystallized while casting or precipitated while being cooled after homogenization to be dissolved into the matrix, and if the temperature exceeds 560 °C, the metals with low melting points will melt and cause burning.
  • Additionally, the reason the solution treatment time is restricted to be within 30 seconds is that in the case of treatment times exceeding 30 seconds, Mg2Si that crystallized while casting or precipitated while being cooled after homogenization is well-dissolved into the matrix, and the Mg and Si become saturated, thereby slowing the coil advancement speed, as a result of which the processing time is increased and the costs mount.
  • The invention is characterized by cooling to room temperature at a rate of at least 10 °C/s after the solution treatment. The reason the cooling rate after the solution treatment is at least 10 °C/s is that if the cooling rate is less than 10 °C/s, Si is deposited in the crystal grain boundary during the cooling step, thus reducing the hemmability.
  • After performing the aforementioned homogenization treatment on the thin slab, it is further cold rolled, subjected to a solution treatment and cooled to room temperature at a rate of at least 10 °C/s, and after the coil is left at room temperature, it may be held for 30 seconds or less at 260-300 °C in a continuous annealing line, then cooled to room temperature at 10 °C/s.
  • This solution treatment and restoration treatment are preferably performed in a normal continuous annealing line. A continuous annealing line (CAL) is an installation for performing continuous solution treatments and the like of coils, characterized by comprising inductive heating devices for performing heat treatments, water tanks for water-cooling, air nozzles for air-cooling, and the like. Due to the restoration treatment, it is possible to re-dissolve GP zones that appear due to natural ageing when left at room temperature after a solution treatment, thus enabling adequate strength to be obtained after heating for coating and baking.
  • Additionally, in order to obtain adequate strength after heating for coating and baking, it is left at room temperature after the solution treatment and subjected to a restoration treatment at 260-300 °C. If the restoration treatment temperature is less than 260 °C, adequate bake-hardenability cannot be obtained, and if it exceeds 300 °C, the hemmability is reduced.
  • The reason the time over which the restoration treatment temperature is held is restricted to within 30 seconds is that if the treatment time exceeds 30 seconds, it is not possible to adequately re-dissolve the GP zones that appear due to natural ageing when left at room temperature after the solution treatment, in addition to which the coil advancement speed is too slow, as a result of which the treatment time is long and the costs mount.
  • After performing the aforementioned homogenization treatment on the thin slab, it can be further cold rolled, subjected to a heat solution treatment in a continuous annealing line, water-cooled to 250 °C or less at a cooling rate (first cooling rate) of at least 10 °C/s, then air-cooled to 60-100 °C at a cooling rate (second cooling rate) of 1-20 °C/s, coiled up and cooled to room temperature.
  • This heat solution treatment and subsequent cooling are preferably performed in a normal continuous annealing line (CAL). During this heat solution treatment and subsequent cooling, a heat treatment (preliminary ageing) can be performed to evenly generate nuclei for β" deposition in the matrix, to obtain adequate strength after heating for coating and baking.
  • After subjecting the thin slab to a homogenization treatment and further cold rolling, it may be subjected to a solution treatment by heating to 530-560 °C at a rate of at least 10 °C/s, then holding for 30 seconds or less, then cooled to room temperature at a rate of at least 10 °C/s, thereafter subjected to a restoration treatment by holding within a range of 260-300 °C for 30 seconds, then cooled to 60-100 °C at a cooling rate of at least 1 °C/s, coiled up and subjected to a preliminary ageing treatment by cooling to room temperature.
  • This solution treatment and subsequent cooling, and restoration treatment and subsequent cooling are preferably performed in a normal continuous annealing line (CAL). With this production method, not only is it possible to re-dissolve GP zones that appear due to natural ageing when left at room temperature after the solution treatment, but it is also possible to perform a heat treatment (preliminary ageing) to generate nuclei for β" deposition, thus further improving the resistance after coating and baking.
  • Next, the significance of the alloy ingredients of the present invention and the reasons for their limitations shall be explained. The essential element Mg is dissolved in the matrix after the heat solution treatment, and is deposited as a reinforcing phase together with Si upon heating for coating and baking, thereby improving the strength. The reason the Mg content is limited to 0.30-1.00 wt% is that the effect is small if less than 0.30 wt%, and if more than 1.00 wt%, the hemmability after the solution treatment is reduced. A more preferable range for the Mg content is 0.30-0.70 wt%.
  • The essential element Si is deposited together with Mg as an intermediary phase of Mg2Si known as β" or an analogous reinforcing phase upon being heated for coating and baking, thereby increasing the strength. The reason the Si content is limited to 0.30-1.20 wt% is that if less than 0.30 wt%, its effects are minimal, and if more than 1.20 wt%, the hemmability is reduced after the heat solution treatment. A more preferable range of Si content is 0.60-1.20 wt%.
  • The essential element Fe, when coexisting with Si and Mn, generates many Al-Fe-Si crystals and Al-(Fe·Mn)-Si crystals of a size of 5 µm or less upon casting, so that re-crystallized nuclei are increased, as a result of which the recrystallized grains are refined and sheets of exceptional formability are obtained. If the Fe content is less than 0.05 wt%, the effects are not very remarkable. If it exceeds 0.50 wt%, coarse Al-Fe-Si crystals and Al-(Fe·Mn)-Si crystals are formed upon casting, thus not only reducing the hemmability but also reducing the amount of Si dissolved in the thin slabs, as a result of which the bake-hardenability of the final sheets is reduced. Therefore, the preferable range of Fe content is 0.05-0.50 wt%. A more preferable range of Fe content is 0.05-0.30 wt%.
  • The essential element Mn is added as an element to refine the re-crystallized grains. By keeping the size of the re-crystallized grains relatively small at 10-25 µm, it is possible to form sheets with exceptional formability. If the Mn content is less than 0.05 wt%, the effect is not adequate, and if it exceeds 0.50 wt%, coarse Al-Fe-Si crystals and Al-(Fe·Mn)-Si crystals are formed upon casting, thus not only reducing the hemmability but also reducing the amount of Si dissolved in the thin slabs, as a result of which the bake-hardenability of the final sheets is reduced. Therefore, the preferable range of Mn content is 0.05-0.50 wt%. A more preferable range of Mn content is 0.05-0.30 wt%.
  • The essential element Ti will not inhibit the effects of the present invention if it is contained at 0.10 wt% or less, and it can function as a crystal grain refiner for the thin slabs, so as to reliably prevent casting defects of the slabs such as cracks or the like. If the Ti content is less than 0.005 wt%, the effects are not adequate, and if the Ti content exceeds 0.10 wt%, coarse intermetallic compounds such as TiAl3 and the like are formed during casting, thus greatly reducing the hemmability. Therefore, the preferable range of Ti content is 0.005-0.10 wt%. A more preferable range for the Ti content is 0.005-0.05 wt%.
  • The optional element Cu is an element that promotes age-hardening and raises the bake-hardenability. If the Cu content is less than 0.05 wt%, the effect is small, and if it exceeds 0.70 wt%, the yield strength of the sheets becomes high after a preliminary ageing treatment, and not only does the hemmability decrease, but the reduction in corrosion resistance is also marked. Therefore, the Cu content is preferably within a range of 0.05-0.70 wt%. The Cu content is more preferably 0.10-0.60 wt%.
  • The optional element Zr is added as an element for refining the re-crystallized grains. If the Zr content is less than 0.05 wt%, the effect is not adequate, and if it exceeds 0.40 wt%, coarse Al-Zr crystals are created during slab casting, thus reducing the hemmability. Therefore, the Zr content is preferably within a range of 0.05-0.40 wt%. The Zr content is more preferably within a range of 0.05-0.30 wt%.
  • As explained above, the present invention allows an Al-Mg-Si alloy sheet for use in automotive body sheets having exceptional bake-hardenablitiy and hemmability after a final anneal to be produced at low cost. While a restoration treatment or high-temperature winding is required to suppress natural ageing as with conventional methods, the steps such as facing, hot rolling and the like that precede these steps can be largely simplified, thus greatly reducing the total production cost.
  • Herebelow, the best modes of the present invention shall be described using examples.
  • Example 1
  • In the below-given examples, the samples after cold rolling are not coils but all cut sheets. Therefore, in order to simulate the step of continuous annealing of a coil in a continuous annealing line (CAL), a solution treatment of the samples in a salt bath and a cold water quench or 85 °C water quench were employed.
  • After degassing melts having the compositions shown in Table 1, they were cast into slabs 7 mm thick by means of a twin-belt casting method. The DAS (Dendrite Arm Spacing) was measured by an intersection method from observation of the microstructures at a quarter-thickness of the slab, and the cooling rate 75 °C/s was computed. A predetermined homogenization treatment was performed on the slabs which were then cooled to room temperature at a predetermined cooling rate, and cold rolled to form sheets of 1 mm thickness. Next, solution treatments were performed on these cold rolled sheets in a salt bath, and they were either 1) quenched in 85 °C water and immediately inserted into an annealer with a predetermined atmospheric temperature to perform a heat treatment under predetermined conditions, or 2) quenched in cold water, left at room temperature for 24 hours, then subjected to a heat treatment under predetermined conditions. Furthermore, in order to simulate automobile coating steps, they were held for one week at room temperature after the heat treatment, and measured for 0.2% yield strength, further baked at 180 °C for 30 minutes, and again measured for 0.2% yield strength.
  • The difference in yield strength before and after the baking treatment was taken as the bake-hardenability, and those exceeding 80 MPa were judged to have excellent bake-hardenability. In order to simulate hemmability, the sheets prior to baking were preliminarily warped by 5%, then bent into a U shape using a jig having a radius r = 0.5 mm, then 1 mm thick spacers were inserted and they were bent 180°. Those which did not crack were ranked O and those which cracked were ranked X. The detailed sheet production steps and evaluation results are shown in Table 2-6.
  • [Table 1]
  • TABLE 1 Alloy Composition
    (wt%)
    Alloy No. Mg Si Fe Mn Cu Ar Ti
    A 0.5 0.7 0.2 0.2 - - 0.02
    B 0.5 0.8 0.2 0.2 - - 0.02
    C 0.6 0.8 0.2 0.2 - - 0.02
    D 0.5 1 0.2 0.2 0.5 - 0.02
    E 0.5 0.8 0.2 0.2 - 0.15 0.02
    F 0.4 1.2 0.2 0.2 0.1 - 0.02
  • Table 2 shows the results for cases in which the homogenization conditions and cooling rate after the homogenization treatment were changed. After the homogenization treatment, the slabs were cold rolled to a thickness of 1 mm, these cold rolled sheets were subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, then quenched with 85 °C water, and immediately inserted into an annealer with an atmospheric temperature of 85 °C to perform a preliminary ageing of 8 hours. Those falling within the scope of conditions of the present invention (1-7) had exceptional bake-hardenability and hemmability. Those that did not undergo a homogenization treatment (8, 10) had poor bake-hardenability and hemmability. Additionally, those which had a slow cooling rate after the homogenization treatment had poor bake-hardenability (9).
  • [Table 2]
  • Figure imgb0001
  • Table 3 shows the results when the temperatures/times of the homogenization treatment are changed. After the homogenization treatment, the slabs were cold rolled to a thickness of 1 mm, these cold rolled sheets were subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, then quenched in 85 °C water and immediately entered into an annealer with an atmospheric temperature of 85 °C to perform a preliminary ageing of 8 hours. Those falling within the scope of conditions of the present invention (11-14) had exceptional bake-hardenability and hemmability. Those that had a low homogenization temperature (15) or had a short holding time (16) had poor bake-hardenability and hemmability.
  • [Table 3]
  • Figure imgb0002
  • Table 4 shows the results when the homogenization conditions and restoration conditions were changed. After the homogenization treatment, the slabs were cold rolled to a thickness of 1 mm, these cold rolled sheets are subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, then quenched in cold water, and after leaving at room temperature for 24 hours, subjected to a restoration treatment by holding for 15 seconds at a predetermined temperature. Those falling within the scope of conditions of the present invention (17-20) had exceptional bake-hardenability and hemmability. Those that had a low restoration temperature (reheating temperature) (21) had poor bake-hardenability. Those whose restoration temperature (reheating temperature) was too high (22) had poor hemmability. Furthermore, even when the restoration conditions were within the scope of the present invention, those in which the homogenization temperature was low (23) or the holding time was short (24) had poor hemmability. Those in which the cooling rate after the homogenization treatment was slow (25) had poor bake-hardenability.
  • [Table 4]
  • Figure imgb0003
  • Table 5 shows the results when the homogenization conditions and cooling pattern after the solution treatment were changed. The cooling rate after the solution treatment was divided into two stages, with the cooling rate from the solution temperature to an intermediate temperature being defined as the first cooling rate and the cooling rate from the intermediate temperature to the coil-up temperature being defined as the second cooling rate. After the homogenization treatment, the slabs were cold rolled to a thickness of 1 mm, and these cold rolled sheets were subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, after which they were cooled to the intermediate temperature at the first cooling rate, then cooled to the coil-up temperature at the second cooling rate, and thereafter cooled to room temperature at 5 °C/h.
  • Those falling within the scope of the present invention (26-28) had exceptional bake-hardenability and hemmability. Those in which the first cooling rate after the solution treatment was slow (29), those in which the second cooling rate was slow (31) or those in which the intermediate temperature was too high (30) had poor hemmability. Those in which the coil-up temperature was too low (32) had poor bake-hardenability. Conversely, those in which the coil-up temperature was too high (33) had poor hemmability. Furthermore, those in which the homogenization treatment temperature was too low (34) or the holding time was too short (35) had poor hemmability. Those in which the cooling rate after the homogenization treatment was too slow (36) had poor bake-hardenability.
  • [Table 5]
  • Figure imgb0004
  • Table 6 shows the results when the restoration treatment temperature (reheating temperature) after the solution treatment and coil-up temperature were changed. After the homogenization treatment, the slabs were cold rolled to a thickness of 1 mm, these cold rolled sheets are subjected to a solution treatment by holding for 15 seconds at a predetermined temperature by means of a salt bath, then quenched in cold water, and after leaving at room temperature for 24 hours, held for 15 seconds at a predetermined temperature (preheating temperature) and cooled to a predetermined coil-up temperature at 10 °C/s, then further cooled to room temperature at 10 °C/h. Those falling within the scope of conditions of the present invention (37-40) had exceptional bake-hardenability and hemmability. Those in which the restoration treatment temperature (reheating temperature) was too high (41) had poor hemmability. Those in which the restoration treatment temperature (reheating temperature) was too low (42) had reduced bake-hardenability. Those in which the coil-up temperature was too low (43) had poor bake-hardenability. Those in which the coil-up temperature was too high (44) had poor hemmability.
  • [Table 6]
  • TABLE 6 Reheat Temperature/Coil-up Temperature and Bake-Hardenability/Hemmability
    ID Alloy No. Sol. Treat. Tem. (°C) Reheat Temp (°C) Coil Up Temp (°C) Yield Str. before/after Baking (Mpa) Bake-Hard. (MPa) Hem.
    Present Invention 37 B 550 270 85 121/231 110
    38 B 550 270 90 125/237 114
    39 B 530 290 70 117/228 111
    40 B 540 290 80 119/231 112
    Comp. Example 41 B 550 320 85 124/234 110 X
    42 B 550 250 80 111/198 87
    43 B 550 260 40 110/185 75
    44 B 550 290 120 131/249 118 X
    Homogenization: 550 °C × 6 h Cooling Rate after Homogenization: 1000 °C/h
  • INDUSTRIAL APPLICABILITY
  • According to the present invention, rolled sheets of Al-Mg-Si alloy that are suitable for forming by bending, press forming and the like of automotive parts, household appliances and the like can be produced at a low cost relative to the conventional art.

Claims (6)

  1. A method of producing aluminum alloy sheets excelling in bake-hardenability and hemmability, comprising steps of casting, by means of a twin-belt casting method, an alloy melt comprising 0.30-1.00 wt% of Mg, 0.30-1.20 wt% of Si, 0.05-0.50 wt% of Fe, 0.05-0.50 wt% of Mn and 0.005-0.10 wt% of Ti, optionally further comprising at least one of 0.05-0.70 wt% of Cu or 0.05-0.40 wt% of Zr, the remainder consisting of Al and unavoidable impurities, to form a 5-15 mm thick slab at a cooling rate of 40-150 °C/s at a quarter-thickness of the slab; winding into a coil; subjecting to a homogenization treatment; cooling to 250 °C or less at a cooling rate of at least 500 °C/h; cold rolling; then subjecting to a solution treatment.
  2. A method in accordance with claim 1, wherein said homogenization treatment involves heating to 520-580 °C at a heating rate of at least 30 °C/h in a batch furnace, then holding at that temperature for 2-24 hours.
  3. A method in accordance with either claim 1 or 2, wherein said solution treatment involves heating to 530-560 °C at a heating rate of at least 10 °C/s in a continuous annealing line, and holding for 30 seconds or less.
  4. A method in accordance with claim 3, comprising steps, after said solution treatment, of cooling to room temperature at a cooling rate of at least 10 °C/s, then subjecting to a restoration treatment by holding for 30 seconds or less at 260-300 °C in a continuous annealing furnace, and cooling to room temperature at a cooling rate of at least 10 °C/s.
  5. A method in accordance with claim 3, comprising steps, after said solution treatment, of water-cooling to 250 °C or less at a cooling rate of at least 10 °C/s, then air-cooling to 60-100 °C at a cooling rate of 1-20 °C/s, coiling up, and subjecting to a preliminary ageing treatment by cooling to room temperature.
  6. A method in accordance with claim 3, comprising steps, after said solution treatment, of cooling to room temperature at a cooling rate of at least 10 °C/s, then subjecting to a restoration treatment by holding for 30 seconds or less at 260-300 °C in a continuous annealing furnace, cooling to 60-100 °C at a cooling rate of at least 1 °C/s, coiling up, and subjecting to a preliminary ageing treatment by cooling to room temperature.
EP04806942A 2003-12-11 2004-12-13 METHOD FOR PRODUCING Al-Mg-Si ALLOY EXCELLENT IN BAKE-HARDENABILITY AND HEMMABILITY Withdrawn EP1702995A1 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2016037922A1 (en) * 2014-09-12 2016-03-17 Aleris Aluminum Duffel Bvba Method of annealing aluminium alloy sheet material
EP2518171A4 (en) * 2009-12-22 2016-04-27 Showa Denko Kk Aluminum alloy for anodization and aluminum alloy component
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Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5180496B2 (en) * 2007-03-14 2013-04-10 株式会社神戸製鋼所 Aluminum alloy forging and method for producing the same
JP5203772B2 (en) * 2008-03-31 2013-06-05 株式会社神戸製鋼所 Aluminum alloy sheet excellent in paint bake hardenability and suppressing room temperature aging and method for producing the same
GB0817169D0 (en) * 2008-09-19 2008-10-29 Univ Birmingham Improved process for forming aluminium alloy sheet components
KR20100099554A (en) * 2009-03-03 2010-09-13 현대모비스 주식회사 Al-si-mg based aluminum alloy excellent in machinability and method of producing the same
US10731241B2 (en) * 2009-05-28 2020-08-04 Bluescope Steel Limited Metal-coated steel strip
CA2810251A1 (en) * 2010-09-08 2012-03-15 Alcoa Inc. Improved 6xxx aluminum alloys, and methods for producing the same
JP5758676B2 (en) * 2011-03-31 2015-08-05 株式会社神戸製鋼所 Aluminum alloy plate for forming and method for producing the same
CN103255324B (en) 2013-04-19 2017-02-08 北京有色金属研究总院 Aluminum alloy material suitable for manufacturing car body panel and preparation method
CN103343304B (en) * 2013-06-18 2015-11-18 常州大学 The deformation heat treatment method of a kind of raising 6000 line aluminium alloy Sheet stretch performances
CN103305779A (en) * 2013-06-18 2013-09-18 常州大学 Thermomechanical treatment method of 6000-series aluminum alloy
JP6752146B2 (en) * 2014-01-21 2020-09-09 アーコニック テクノロジーズ エルエルシーArconic Technologies Llc 6000 series aluminum alloy
GB2527486A (en) 2014-03-14 2015-12-30 Imp Innovations Ltd A method of forming complex parts from sheet metal alloy
JP6224550B2 (en) * 2014-08-27 2017-11-01 株式会社神戸製鋼所 Aluminum alloy sheet for forming
EP3006579B2 (en) * 2014-12-11 2022-06-01 Aleris Aluminum Duffel BVBA Method of continuously heat-treating 7000-series aluminium alloy sheet material
CN105349848B (en) * 2015-11-19 2017-07-14 江苏常铝铝业股份有限公司 A kind of used in blinds continuous casting and rolling aluminium alloy material and its manufacture method
US10538834B2 (en) * 2015-12-18 2020-01-21 Novelis Inc. High-strength 6XXX aluminum alloys and methods of making the same
EP3390678B1 (en) 2015-12-18 2020-11-25 Novelis, Inc. High strength 6xxx aluminum alloys and methods of making the same
JP6208389B1 (en) * 2016-07-14 2017-10-04 株式会社Uacj Method for producing rolled aluminum alloy material for forming comprising aluminum alloy having excellent bending workability and ridging resistance
ES2951553T3 (en) 2016-10-27 2023-10-23 Novelis Inc High-strength 6XXX series aluminum alloys and methods of manufacturing the same
CN109890536B (en) 2016-10-27 2022-09-23 诺维尔里斯公司 High strength7XXX series aluminum alloys and methods of making the same
MX2019004840A (en) 2016-10-27 2019-06-20 Novelis Inc Systems and methods for making thick gauge aluminum alloy articles.
JP2020537039A (en) * 2017-10-23 2020-12-17 ノベリス・インコーポレイテッドNovelis Inc. High-strength and highly moldable aluminum alloy and its manufacturing method
CN109082566B (en) * 2018-08-07 2020-05-05 中铝瑞闽股份有限公司 6-series alloy aluminum plate strip for mobile phone frame and preparation method thereof
CN109868398B (en) * 2019-02-02 2021-04-06 中铝材料应用研究院有限公司 6xxx series aluminum alloy plate with high flanging performance and preparation method thereof
CN110079709A (en) * 2019-05-08 2019-08-02 常熟希那基汽车零件有限公司 A kind of alloy material and its production technology
KR20220033650A (en) * 2020-09-09 2022-03-17 삼성디스플레이 주식회사 Reflective electrode and display device having the same
CN113337761A (en) * 2021-04-20 2021-09-03 山东国泰铝业有限公司 Aluminum alloy building door and window material and preparation method thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS62207851A (en) * 1986-03-10 1987-09-12 Sky Alum Co Ltd Rolled aluminum alloy sheet for forming and its production
US5616189A (en) * 1993-07-28 1997-04-01 Alcan International Limited Aluminum alloys and process for making aluminum alloy sheet
JP3734317B2 (en) * 1996-10-09 2006-01-11 古河スカイ株式会社 Method for producing Al-Mg-Si alloy plate
JP3398835B2 (en) * 1997-09-11 2003-04-21 日本軽金属株式会社 Automotive aluminum alloy sheet with excellent continuous resistance spot weldability
JP3656150B2 (en) * 1997-09-11 2005-06-08 日本軽金属株式会社 Method for producing aluminum alloy plate
JP2001262264A (en) * 2000-03-21 2001-09-26 Kobe Steel Ltd Al-Mg-Si SERIES Al ALLOY SHEET EXCELLENT IN TOUGHNESS AND BENDABILITY
US20030133825A1 (en) * 2002-01-17 2003-07-17 Tom Davisson Composition and method of forming aluminum alloy foil
JP4175818B2 (en) * 2001-03-28 2008-11-05 住友軽金属工業株式会社 Aluminum alloy plate excellent in formability and paint bake hardenability and method for producing the same

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
See references of WO2005056859A1 *

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2518171A4 (en) * 2009-12-22 2016-04-27 Showa Denko Kk Aluminum alloy for anodization and aluminum alloy component
WO2016037922A1 (en) * 2014-09-12 2016-03-17 Aleris Aluminum Duffel Bvba Method of annealing aluminium alloy sheet material
US10294553B2 (en) 2014-09-12 2019-05-21 Aleris Aluminum Duffel Bvba Method of annealing aluminium alloy sheet material
WO2018185425A1 (en) 2017-04-06 2018-10-11 Constellium Neuf-Brisach Improved method for producing a motor vehicle body structure component
FR3065013A1 (en) * 2017-04-06 2018-10-12 Constellium Neuf-Brisach IMPROVED METHOD FOR MANUFACTURING AUTOMOTIVE CASE STRUCTURE COMPONENT
US11649536B2 (en) 2017-04-06 2023-05-16 Constellium Neuf-Brisach Method for manufacturing a structure component for a motor vehicle body
EP3839085A1 (en) 2019-12-17 2021-06-23 Constellium Neuf Brisach Improved method for manufacturing a structure component for a motor vehicle body
WO2021122621A1 (en) 2019-12-17 2021-06-24 Constellium Neuf-Brisach Improved method for manufacturing a structure component for a motor vehicle body

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CA2548788A1 (en) 2005-06-23
US20070209739A1 (en) 2007-09-13
JP4577218B2 (en) 2010-11-10
WO2005056859A1 (en) 2005-06-23
TW200536946A (en) 2005-11-16

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