TECHNICAL FIELD
[0001] 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
[0002] 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.
[0003] 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.
[0004] 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 Mg
2Si compounds on the surface layer portion is 50 µm or less.
[0005] 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
[0006] 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.
[0007] 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
[0008] 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
2Si while cooling, to obtain an aluminum sheet for automotive body sheets with excellent
bake-hardenabiltiy and hemmability after a final anneal.
[0009] 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).
[0010] 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).
[0011] 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).
[0012] 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).
[0013] 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).
[0014] 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
[0015] 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
[0016] 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.
[0017] 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.
[0018] 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.
[0019] 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.
[0020] 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
2Si 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.
[0021] 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
2Si as much as possible, and to dissolve the Mg and Si into the matrix in an oversaturated
state.
[0022] 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.
[0023] 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.
[0024] 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
2Si 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.
[0025] 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 Mg
2Si that crystallized during casting into the matrix, and if the treatment time exceeds
24 hours, the Mg
2Si that crystallized during casting is well-dissolved into the matrix, and the Mg
and Si become saturated, resulting in cost increases.
[0026] 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).
[0027] 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.
[0028] 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.
[0029] 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.
[0030] 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
2Si 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.
[0031] 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, Mg
2Si 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.
[0032] 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.
[0033] 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.
[0034] 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.
[0035] 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.
[0036] 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.
[0037] 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.
[0038] 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.
[0039] 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.
[0040] 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.
[0041] 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%.
[0042] The essential element Si is deposited together with Mg as an intermediary phase of
Mg
2Si 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%.
[0043] 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%.
[0044] 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%.
[0045] 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%.
[0046] 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%.
[0047] 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%.
[0048] 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.
[0049] Herebelow, the best modes of the present invention shall be described using examples.
Example 1
[0050] 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.
[0051] 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.
[0052] 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]
[0053]
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 |
[0054] 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]
[0055]

[0056] 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]
[0057]

[0058] 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]
[0059]

[0060] 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.
[0061] 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]
[0062]

[0063] 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]
[0064]
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
[0065] 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.