[Technical Field]
[0001] The present invention relates to a high-formed magnesium alloy sheet and a method
of manufacturing the same.
[Background of the Invention]
[0002] In recent years, light weight (gram, gram) marketing has been actively performed
in mobile and IT fields. More specifically, as the functions of the mobile device
field become diversified, the product weight is required to be lighter. As a result,
there is an increasing interest in magnesium sheet having excellent non-strength (strength
against density).
[0003] The density of magnesium is 1.74 g/cm
3, which is the lightest metal among the structural metals including aluminum and steel.
In addition, it is a metal that is attracting attention in mobile and IT fields because
of its excellent vibration absorbing ability and electromagnetic wave shielding ability.
In addition, in the automobile field, studies are being actively carried out in advanced
countries including Europe to reduce the weight of the vehicle body due to the regulation
of fuel economy and performance, and magnesium is being reported as a substitute metal.
However, since magnesium is expensive compared to competitive materials such as aluminum
and stainless steel, its application to magnesium is limited to only some parts that
are required to be lightweight.
[0004] In addition, magnesium is difficult to form at room temperature due to hexagonal
close packing (HCP). Since the warm forming process is essential for the application
of the product, the investment cost of the mold/heating device for the warm forming
becomes large. In addition, it is deteriorated the productivity due to sticking, scratching
between the mold and the material, and delay time for heating. Therefore, not only
the price of the magnesium material, but also the processing cost of the magnesium
alloy is more expensive than the competitive material.
[0005] On the basis of this, a magnesium alloy for improving room temperature moldability
has been developed. However, a lithium alloy or a rare earth element having a high
value is added, or the manufacturing process is complicated.
[Description of the Invention]
[Problem to Solve]
[0006] An embodiment of the present invention is to provide a high-formed magnesium alloy
sheet and a method of manufacturing the same by controlling the composition range
of the Zn, Ca, and Mn components of the magnesium alloy sheet and the relationship
of the components.
[0007] Specifically, the present invention provides a magnesium alloy sheet excellent in
moldability by controlling the Mg-Ca based secondary phase through the composition
of the alloy and the manufacturing conditions.
[Solution to the Problem]
[0008] A magnesium alloy sheet of one embodiment of the invention may include 3.0 wt% or
less (excluding 0 wt%) of Zn, 1.5 wt% or less (excluding 0 wt%) of Ca, 1.0 wt% or
less (excluding 0 wt%) of Mn, balance of Mg and inevitable impurities, for a total
of 100 wt%, wherein, the magnesium alloy sheet further comprises 0.3 wt% or less of
Al, based on 100 wt% of the entire magnesium alloy sheet.
[0009] The magnesium alloy sheet may satisfy the following formulas (1) and (2):
[Zn]/[Ca]≤4.0------------ formula (1)
[Zn]+ [Ca]>[Mn]------------ formula (2)
[Zn], [Ca], and [Mn] refer to weight percent of each component.
[0010] A maximum texture intensity based on the {0001} plane of the magnesium alloy sheet
may be 1 to 4.
[0011] The magnesium alloy sheet can have 7 to 10 mm of Limit Dome Height (LDH).
[0012] The magnesium alloy sheet may include crystal grain having an average particle size
of 1 to 20 µm.
[0013] The magnesium alloy sheet may include a Mg-Ca based secondary phase, and the average
particle size of the secondary phase is 30 µm or less.
[0014] Otherwise, the magnesium alloy sheet can include 1 to 20 secondary phases per 100
µm
2 of the magnesium alloy sheet area.
[0015] A method of manufacturing a magnesium alloy sheet of one embodiment of the invention
may include: preparing a cast material by casting a molten alloy comprising 3.0 wt%
or less (excluding 0 wt%) of Zn, 1.5 wt% or less (excluding 0 wt%) of Ca, 1.0 wt%
or less (excluding 0 wt%) of Mn, balance of Mg and inevitable impurities, for a total
of 100 wt%; subjecting the cast material to homogenizing heat treatment; preparing
a rolled material by subjecting the homogenizing heat treated cast material to hot
rolling; and final annealing the rolled material.
[0016] Wherein, the molten alloy can further include 0.3 wt% or less of Al, based on 100
wt% of the entire molten alloy, and the magnesium alloy sheet satisfies the following
formulas (1) and (2).
[Zn]/[Ca]≤4.0------------ formula (1)
[Zn]+ [Ca]>[Mn]------------ formula (2)
[Zn], [Ca], and [Mn] refer to weight percent of each component.
[0017] In the step of final annealing the rolled material, a temperature range may be from
200 to 500°C. The step of the final annealing the rolled material may be conducted
for less than 5 hours (excluding 0 hours).
[Effect]
[0018] According to an embodiment of the present invention, the composition range of the
Zn, Ca, and Mn components of the magnesium alloy sheet and the relationship of the
above components can be controlled to provide a magnesium alloy sheet of high molding.
[0019] Specifically, it is possible to provide a magnesium alloy sheet excellent in strength
and room temperature moldability by controlling the Mg-Ca based secondary phase.
[Brief Description of Drawings]
[0020]
Fig. 1 is a photograph of the microstructure of the magnesium alloy sheet of Example
2 and Comparative Example 2 observed with an optical microscope.
Fig. 2 shows the results of analysis of the secondary phase components of Example
2 and Comparative Example 2 by SEM-EDS.
Fig. 3 shows the results of analysis of the {0001} planes of Example 2 and Comparative
Example 3 by the XRD pole diagram and EBSD.
[Detailed Description of the Invention]
[0021] The advantages and features of the present invention and the manner of achieving
them will become apparent with reference to the embodiments described in detail below
with the accompanying drawings. However, it is to be understood that the present invention
is not limited to the disclosed embodiments, but may be embodied in many different
forms, and these embodiments are provided so that this disclosure will be thorough
and complete and will fully convey the scope of the invention to a person skilled
in the art, and the present invention is only defined by the scope of the claims.
Same reference numerals refer to same elements throughout the specification.
[0022] Thus, in some embodiments, well-known techniques are not specifically described to
avoid an ambiguous interpretation of the present invention. Unless defined otherwise,
all terms (including technical and scientific terms) used herein may be used in a
sense commonly understood by a person skilled in the art. Further, through the specification,
unless explicitly described to the contrary, the word "comprise" and variations such
as "comprises" or "comprising" will be understood to imply the inclusion of stated
elements but not the exclusion of any other elements. Also, singular forms comprise
plural forms unless noted otherwise.
[0023] One embodiment of the present invention provides a magnesium alloy sheet including:
3.0 wt% or less (excluding 0 wt%) of Zn, 1.5 wt% or less (excluding 0 wt%) of Ca,
1.0 wt% or less (excluding 0 wt%) of Mn, balance of Mg and inevitable impurities,
for a total of 100 wt%.
[0024] The magnesium alloy sheet can further include 0.3 wt% or less of Al, based on 100
wt% of the entire magnesium alloy sheet.
[0025] The composition range of the aluminum component may be such that it is added at an
impurity level as compared with essential additive elements such as zinc, calcium,
and manganese in the magnesium alloy sheet according to one embodiment of the present
invention.
[0026] The reason for limiting the component and composition of the magnesium alloy sheet
according to one embodiment of the present invention will be described in detail.
[0027] Zn may include 3.0 wt% or less, but 0 wt% is excluded.
[0028] More specifically, Zn may be 0.5 to 3.0 wt%.
[0029] More specifically, when zinc is added, such as calcium, it may segregate in the grain
boundary and the twin crystal phase to contribute to the generation and growth of
the non-bottom grain recrystallized grains. As a result, softening phenomenon of the
non-bottom surface is brought about, and the slip of the non-bottom surface is activated
to improve the formability of the sheet material. Therefore, when it is added in an
amount less than 0.5% by weight, it may be difficult to ensure moldability.
[0030] However, if it is added in an amount exceeding 3.0% by weight, it may be bonded with
magnesium and calcium to form additional intermetallic compounds, which may adversely
affect the moldability. Further, when casting, sticking occurs more deeply and molding
may be difficult. Accordingly, when zinc is contained in the above range, an effect
of improving moldability at room temperature can be expected.
[0031] Ca may contain up to 1.5% by weight, but excluding 0% by weight.
[0032] More specifically, Ca may be 0.1 to 1.5% by weight.
[0033] More specifically, calcium, like zinc, may be segregated in grain boundaries and
twin crystal phase to contribute to the production and growth of non-bottom recrystallized
grains. As a result, softening phenomenon of the non-bottom surface is brought about,
and the slip of the non-bottom surface is activated to improve the formability of
the sheet. Therefore, when it is added in an amount of less than 0.1% by weight, it
is difficult to secure moldability.
[0034] However, the addition of more than 1.5% by weight reduces the fluidity of the molten
alloy and lowers the casting property, so that the productivity may be reduced, cracks
may be generated at the time of rolling, and the rolling property of the plate material
may be deteriorated. Accordingly, when calcium is contained in the above range in
the present invention, an effect of improving the room temperature moldability can
be expected within a range that does not inhibit the casting and rolling property.
[0035] Mn may include not more than 1.0 wt%, but not 0 wt%.
[0036] More specifically, manganese acts as a recrystallization nucleation site to generate
fine grains, and then to suppress grain growth, thereby providing fine and uniform
grains. Therefore, in the method of manufacturing a magnesium alloy sheet, which is
another embodiment of the present invention described later, it is possible to provide
fine crystal grains in the homogenizing heat treatment step, and finely control the
crystal grains of the final magnesium alloy sheet.
[0037] Accordingly, when the manganese is contained in the range as described above, the
crystal grains of the homogenizing heat treated sheet are finely formed, and defects
such as abnormal crystal growth in the hot rolling step, orange peel due to shear
band and surface cracks can be prevented. Therefore, the rolling property can be improved.
In addition, when manganese is contained in the above range, impurities such as iron
(Fe) and silicon (Si) can be controlled to provide excellent corrosion resistance.
[0038] Therefore, a sheet having fine crystal grains can be produced through addition of
manganese, so that both the strength and the formability can be excellent.
[0039] The magnesium alloy sheet satisfies the following formulas (1) and (2).
[Zn]/[Ca]≤4.0------------ formula (1)
[Zn]+[Ca]>[Mn]------------ formula (2)
[Zn], [Ca], and [Mn] refer to weight percent of each component.
[0040] More specifically, the formula (1) may be 3 or less.
[0041] It may be possible to prevent the secondary phase coarsening generated by further
limiting the composition ratios of Zn and Ca components as well as the composition
ratios as in the above formula (1), and realized the desired high strength and high
molding properties.
[0042] Specifically, the magnesium alloy sheet can satisfy the formula (2) ([Zn] + [Ca]>
[Mn]). Concretely, when the sum of the Zn and Ca composition is equal to or smaller
than the composition of Mn, the rolling property and the formability may be deteriorated.
[0043] The magnesium alloy sheet satisfying the above-described components and composition
ranges may include a Mg-Ca based secondary phase. At this time, the average particle
size of the secondary phase may be 30 µm or less. Specifically, it may be 25 µm or
less. Specifically, it may be 20 µm or less.
[0044] The average particle size in this specification means the average diameter of the
spherical substance present in the unit of measurement. If the material is a non-spherical
material, it can be calculated by approximating the non-spherical material to the
spherical shape.
[0045] That is, the range of the secondary phase size is significantly smaller than that
of the secondary phase of the general magnesium alloy sheet.
[0046] When the average particle size of the secondary phase exceeds 30 µm, the moldability
of the alloy material may be lowered.
[0047] As will be described later, this can be visually confirmed through the drawings.
[0048] The magnesium alloy sheet can include 1 to 20 secondary phases per 100 µm
2 of the magnesium alloy sheet area.
[0049] When the number of the secondary phases is the same as above, the strength and moldability
of the magnesium alloy sheet can be excellent.
[0050] The magnesium alloy sheet may include crystal grains having an average particle diameter
of 1 to 20 µm.
[0051] By controlling the component and composition of the aforementioned magnesium alloy
sheet, it is possible to obtain the crystal grain size in the above range. More specifically,
when the grain size of the magnesium alloy sheet is in the above range, the strength
can be excellent.
[0052] The maximum texture intensity based on the {0001} plane of the magnesium alloy sheet
may be 1 to 4.
[0053] As the texture intensity of the magnesium alloy sheet is in the above range, crystal
grains of various orientations can be distributed. Accordingly, since the fraction
of the bottom grain (<0001>//C-axis orientation) is small, a magnesium alloy sheet
having excellent formability can be provided.
[0054] In the present specification, the bottom crystal grain means a crystal grain having
a bottom orientation. Specifically, magnesium has an HCP (Hexagonal Closed Pack) crystal
structure. At this time, when the C axis of the crystal structure is parallel to the
thickness direction of the sheet, the crystal grains is referred to as crystal grains
having a bottom crystal orientation (that is, bottom crystal grains). Therefore, in
the present specification, the bottom grain can also be expressed as "<0001>//C axis".
[0055] Specifically, the smaller the maximum texture intensity with respect to the {0001}
plane of the magnesium alloy sheet, the more crystal grains of various orientations
are distributed. Further, as the crystal grains of various orientations are distributed
and the fraction of the bottom surface crystal grains is lower, a magnesium alloy
sheet having excellent formability can be obtained.
[0056] Therefore, the magnesium alloy sheet according to an embodiment of the present invention
has a texture intensity of 1 to 4 based on the {0001} plane, so that the moldability
can be excellent.
[0057] The Erichsen value of the magnesium alloy sheet at room temperature may be 7 to 10
mm.
[0058] In this specification, the Erichsen value means an experimental value derived from
the Ericsson test at room temperature. More specifically, the Erichsen value refers
to the height at which the sheet is deformed until a fracture occurs, when the sheet
is deformed into a cup shape.
[0059] Therefore, the room temperature moldability can be compared through the Erichsen
value.
[0060] The yield strength of the magnesium alloy sheet may be 170 MPa or more. Specifically,
it may be 170 to 220 MPa.
[0061] Also, the tensile strength of the magnesium alloy sheet may be 240 MPa or more. Specifically,
it may be 240 to 300 MPa.
[0062] The elongation of the magnesium alloy sheet may be 20% or more. Specifically, it
may be 20 to 30%.
[0063] However, the present invention is not limited thereto. Specifically, the yield strength,
the tensile strength, and the elongation are preferably as good as possible, and the
magnesium alloy sheet according to one embodiment of the present invention can realize
mechanical properties at least the minimum value.
[0064] In addition, the strength and elongation of the magnesium alloy sheet according to
one embodiment of the present invention are excellent in strength and elongation as
compared with the conventional case in which an additional element is added to the
AZ-based magnesium alloy.
[0065] Thus, by controlling the component and composition of the magnesium alloy sheet as
described above, it is possible to provide a magnesium alloy sheet excellent in both
strength and moldability.
[0066] A method of manufacturing a magnesium alloy sheet of one embodiment of the invention
may include: preparing a cast material by casting a molten alloy comprising 3.0 wt%
or less (excluding 0 wt%) of Zn, 1.5 wt% or less (excluding 0 wt%) of Ca, 1.0 wt%
or less (excluding 0 wt%) of Mn, balance of Mg and inevitable impurities, for a total
of 100 wt% (S10); subjecting the cast material to homogenizing heat treatment (S20);
preparing a rolled material by subjecting the homogenizing heat treated cast material
to hot rolling (S30); and final annealing the rolled material (S40).
[0067] First, a step of preparing a cast material by casting a molten alloy comprising 3.0
wt% or less (excluding 0 wt%) of Zn, 1.5 wt% or less (excluding 0 wt%) of Ca, 1.0
wt% or less (excluding 0 wt%) of Mn, balance of Mg and inevitable impurities, for
a total of 100 wt% (S10) can be performed.
[0068] It may further contain less than 0.3% by weight of Al relative to 100% by weight
of the entire magnesium molten alloy.
[0069] Specifically, the magnesium molten alloy can satisfy the following formulas (1) and
(2).
[Zn]/[Ca]≤4.0------------ formula (1)
[Zn]+[Ca]>[Mn]------------ formula (2)
[Zn], [Ca], and [Mn] refer to weight percent of each component.
[0070] The reason for limiting the component and the composition range of the molten alloy
is the same as the reason for limiting the component and the composition range of
the magnesium alloy sheet described above, so that the description is omitted.
[0071] More specifically, the molten alloy can be cast by gravity casting, continuous casting,
strip casting (thin sheet casting), sand casting, vacuum casting, centrifugal casting,
die casting, or thixo molding.
[0072] However, the present invention is not limited thereto, and any method capable of
producing a cast material is possible.
[0073] Thereafter, a step (S20) of subjecting the cast material to homogenizing heat treatment
can be performed.
[0074] Specifically, it can be carried out at 300 to 500 °C.
[0075] More specifically, it may be carried out for 5 to 30 hours.
[0076] More specifically, overheating can be prevented by homogenizing the cast material
in the temperature and time range, and the microstructure and segregation of the cast
material can be sufficiently homogenizing heated.
[0077] Thereafter, the step (S30) of preparing a rolled material by subjecting the homogenizing
heat treated cast material to hot rolling may be performed.
[0078] Specifically, hot rolling can be performed in a temperature range of 150 to 400 °C.
[0079] More specifically, in the case of hot rolling at less than 150 °C, a large amount
of surface scattering type cracks or edge cracks may occur.
[0080] On the other hand, when hot rolling is performed at a temperature higher than 400
°C, there may be occurred a problem of equipment such as the necessity of changing
the component of the equipment to a heat resistant material for rolling at a high
temperature. As a result, problems such as an increase in process cost and a decrease
in productivity are caused, and mass production of the magnesium alloy sheet may be
difficult.
[0081] In addition, the cast material may be hot rolled once or twice at a reduction ratio
of not more than 40% (excluding 0%) per rolling.
[0082] The homogenizing heat treated cast material can be hot rolled by using a hot rolling
mill.
[0083] When the cast material is hot-rolled twice or more, an intermediate annealing may
be performed at least once between hot rolling. The intermediate annealing may be
performed at a temperature range of 300 to 500 °C
[0084] The intermediate annealing may be performed for 5 hours or less (excluding 0 hours).
[0085] More specifically, if the temperature and time range are not satisfied, the stress
of the hardened tissue is not sufficiently solved by the cumulative rolling reduction,
and the annealing process may not be performed properly. Further, the abnormal crystal
grains can grow due to excessive annealing.
[0086] Further, the thickness of the rolled material that is hot-rolled at least twice may
be 2.0 mm or less.
[0087] Thereafter, a step (S40) of final annealing the rolled material can be carried out.
[0088] Concretely, it can be carried out at 200 to 500 ° C.
[0089] More specifically, it can be carried out for not more than 5 hours (excluding 0 hours).
[0090] More specifically, by finally annealing the rolled material in the temperature and
time range, the magnesium alloy sheet produced can secure the desired formability
at room temperature.
[0091] Hereinafter, the embodiment will be described in detail. The following examples are
illustrative of the present invention only and are not intended to limit the scope
of the present invention.
Examples and Comparative Examples
[0092] As shown in the following Table 1, when the range according to one embodiment of
the present invention is satisfied, it is classified as an invention material. Meanwhile,
when the range according to one embodiment of the present invention is not satisfied,
it is classified as a comparative material.
[0093] Then, using the inventive material and the comparative material shown in Table 1,
a magnesium alloy plate material was produced under the following conditions.
[0094] First, an alloyed molten metal of an inventive material and a comparative material
was cast to produce a cast material.
[0095] Thereafter, the cast material was subjected to homogenizing heat treatment at 330
to 450 °C for 16 hours.
[0096] The homogenizing heat treated cast material was rolled at 300 °C at a reduction ratio
of 10 to 20% to prepare a rolled material. At this time, intermediate annealing was
performed at 450 °C for 0.5 to 1 hour.
[0097] Finally, the rolled material was subjected to final annealing as shown in Table 2
below to produce a magnesium alloy sheet.
[Table 1]
Classification |
Alloy |
Al |
Zn |
Ca |
Mn |
formula (1) Zn+ Ca>Mn |
formula (2) Zn/Ca |
Example 1 |
Mg-1.0Zn-0.6Ca-0.3Mn |
- |
1.07 |
0.61 |
0.35 |
○ |
1.75 |
Example 2 |
Mg-1.5Zn-0.6Ca-0.3Mn |
- |
1.55 |
0.60 |
0.35 |
○ |
2.58 |
Example 3 |
Mg-2.0Zn-0.6Ca-0.3Mn |
- |
2.23 |
0.59 |
0.31 |
○ |
3.77 |
C-Example 1 |
Mg-0.3Zn-0.2Ca-1.2Mn |
- |
0.38 |
0.22 |
1.26 |
X |
1.73 |
C-Example 2 |
Mg-3.0Zn-0.6Ca-0.3Mn |
- |
3.04 |
0.55 |
0.32 |
○ |
5.52 |
C-Example 3 |
Mg-3.0Al-1.0Zn(AZ31) |
2.98 |
0.79 |
- |
0.33 |
○ |
- |
C-Example 4 |
Mg-3.0Al-0.6Ca-1.0Zn |
2.98 |
0.79 |
0.65 |
0.33 |
○ |
1.22 |
C-Example 5 |
Mg-2.0Zn-0.1Ca-0.3Mn |
- |
2.09 |
0.11 |
0.32 |
○ |
20 |
[0098] As a result, Table 2 shows mechanical properties of the magnesium alloy sheet according
to Examples and Comparative Examples and Erichsen's values at room temperature.
[0099] The Ericsson values measurement method is as follows.
[0100] Specifically, a magnesium alloy sheet having a size of 50 to 60 mm in each of the
width and the length was used, and a lubricant was used on the surface of the sheet
to reduce the friction between the sheet and the spherical punch.
[0101] At this time, the temperature of the die and the spherical punch was set at room
temperature.
[0102] More specifically, after inserting the magnesium alloy sheet between the upper die
and the lower die, the outer peripheral portion of the sheet was fixed with a force
of 10 kN. Thereafter, the sheet was deformed at a rate of 5 mm/min using a spherical
punch having a diameter of 20 mm. Thereafter, the punch was inserted until the sheet
was broken, and then the deformation height of the sheet was measured at the time
of breaking.
[0103] The deformation height of the plate measured in this way is called the Erichsen value
or the limit dome height (LDH).
[Table 2]
species |
Classification |
Final annealing temperature and time |
Yield strength (MPa) |
tensile strength (MPa) |
Elongation (%) |
Erichsen value (mm) |
Invention material 1 |
Example 1 |
400 °C, 30 min |
174 |
246 |
23.1 |
8.3 |
Invention material 2 |
Example 2 |
400 °C, 30 min |
185 |
254 |
22.2 |
9.0 |
Invention material 3 |
Example 3 |
400 °C, 30 min |
191 |
263 |
20.9 |
8.1 |
Comparative material 1 |
C-Example 1 |
400 °C, 30 min |
125 |
208 |
23.4 |
5.5 |
Comparative material 2 |
C-Example 2 |
400 °C, 30 min |
173 |
253 |
19.1 |
6.9 |
Comparative material3 |
C-Example 3 |
350 °C, 30 min |
165 |
257 |
24.5 |
3.5 |
Comparative material4 |
C-Example 4 |
400 °C, 30 min |
151 |
251 |
19.6 |
7.4 |
Comparative material5 |
C-Example 5 |
400 °C, 30 min |
152 |
237 |
22.6 |
7.1 |
[0104] As a result, it can be seen that Examples 1 to 3 have a much higher Erichsen value
than the Comparative Examples. Specifically, it can be seen that the present example
has a yield strength of 170 MPa or more, a tensile strength of 240 MPa or more, an
elongation of 20% or more, and a room temperature Erichsen value of 7 mm or more.
[0105] Specifically, the comparative examples which satisfy the range of the composition
of Zn, Ca, and Mn according to one embodiment of the present invention, but do not
satisfy both the formula [Zn] + [Ca]> [Mn] and the formula [Zn]/[Ca] ≤ 4.0, can be
confirmed that there is an effect of heating strength and formability.
[0106] These characteristics can also be confirmed through the drawings.
[0107] Fig. 1 is a photograph of the microstructure of the magnesium alloy shee of Example
2 and Comparative Example 2 observed with an optical microscope.
[0108] As a result, comparing the microstructures of Example 2 and Comparative Example 2
in which the final annealing conditions were the same and the components of the alloy
were different, the secondary phase in the form of agglomerated black in Comparative
Example 2 is more than Example 2. It can be seen with the naked eye.
[0109] In addition, in the case of Comparative Example 2 using Comparative Material 2 having
a higher Zn content than Example 2 using Invention Material 2, it can be seen that
the size of the secondary phase is coarse.
[0110] As described above, the coarse secondary phase adversely affects the moldability.
[0111] As a result, as shown in Table 2, the Erichsen value of Comparative Example 2 is
6.9 mm, while the Erichsen value of Example 2 is 9.0 mm, indicating that the moldability
of this embodiment is better.
[0112] Further, when the content of Zn is added in an amount exceeding 3% by weight, the
crystal grains can be locally coarsened as in Comparative Example 2. As a result,
mechanical properties and moldability may be deteriorated.
[0113] Fig. 2 shows the results of analysis of the secondary phase components of Example
2 and Comparative Example 2 by SEM-EDS.
[0114] When a sample is irradiated with a certain wavelength using a SEM-EDS analyzer, a
peak may appear at a value corresponding to the energy of the material. At this time,
component analysis can be derived from the wavelengths shown.
[0115] Specifically, it can be seen that a secondary phase (dark gray spherical shape) is
finely dispersed in an EDS (Energy Dispersive Spectroscopy) photograph of a scanning
electron microscope (SEM) of Example 2. As a result of analyzing the secondary phase
component of Example 2, it can be seen that it is a Mg-Ca secondary phase. At this
time, the size of the secondary phase was about 20 µm or less.
[0116] On the other hand, the secondary phase (white) of the microstructure of Comparative
Example 2 in which the content of Zn exceeded 3.0 wt% was confirmed. However, as a
result of analyzing the secondary phase component of Comparative Example 2, it can
be seen that the secondary phase is a Ca-Mg-Zn three-atom system.
[0117] In other words, in Example 2, as a result of the content ratio of Zn and Ca and the
content ratio of Zn/Ca satisfying all the ranges defined in the embodiment of the
present invention, it was also confirmed that the formation of the secondary phase
of the Mg-Ca two-atom system is more easy than the secondary phase of Ca-Mg-Zn three-atom
system.
[0118] Further, as can be seen from Fig. 2, the secondary phase of Comparative Example 2
in which the Zn content is excessive is larger than that of the secondary phase of
Example 2.
[0119] On the other hand, in Example 2 of the present application, the Ma-Ca based secondary
phase is finely dispersed and distributed at a level of 20 µm or less, thereby contributing
to improvement of the strength and moldability of the magnesium alloy sheet.
[0120] Fig. 3 shows the results of analysis of the {0001} planes of Example 2 and Comparative
Example 3 by the XRD pole diagram and EBSD.
[0121] Specifically, Fig. 3 shows the texture according to the crystal orientation of the
crystal grains by using the XRD pole figure method and EBSD (Electron Backscatter
Diffraction) method.
[0122] The EBSD can inject electrons into the specimen through the e-electron beam and measure
the crystal orientation of the grains using inelastic scattering diffraction at the
back of the specimen.
[0123] The pole figure is a stereo projection of the direction of the arbitrarily fixed
crystal coordinate system in the specimen coordinate system. More specifically, the
poles for the {0001} planes of the crystal grains of various orientations can be displayed
in the reference coordinate system, and the poles can be represented by plotting density
contours according to the poles density distribution. At this time, the poles are
fixed in a specific lattice direction by the Bragg angle, and a plurality of poles
can be displayed for a single crystal.
[0124] Therefore, the numerical representation of the density distribution values of the
contour lines indicated by the poling method can be referred to as the texture intensity
for the {0001} plane.
[0125] Accordingly, as the texture intensity becomes smaller, crystal grains of various
orientations are distributed. As the texture intensity becomes larger, it can be interpreted
that the crystal grains of <0001>//C axis orientation are distributed much.
[0126] First, as shown in Fig. 3, it can be seen that the grain size of the grain in Example
2 is as fine as 1 to 20 µm as compared with that of Comparative Example 3.
[0127] In addition, the maximum texture intensity of the {0001} plane of Example 2 was 2.46.
It is significantly lower than that of Comparative Example 3 with a maximum texture
intensity of 12.11. From this, it can be interpreted that the crystal grains of various
orientations are distributed in Example 2 of the present invention, whereas the crystal
grains (bottom crystal grains) of the <0001>//C axis orientation are distributed much
in Comparative Example 3.
[0128] From this, it can be seen that the embodiment has better moldability because the
fraction of the bottom surface crystal grain is smaller than that of the comparative
example.
[0129] Although the embodiments of the present invention have been described with reference
to the accompanying drawings, it will be understood by a person skilled in the art
may understand that it may be carried out in different and concrete forms without
changing the technical idea or fundamental feature of the present invention.
[0130] Therefore, it is to be understood that the above-mentioned examples or embodiments
are illustrative in all aspects and not limitative. The scope of the present invention
is defined by the appended claims rather than the detailed description, and all changes
or modifications derived from the meaning and scope of the claims and their equivalents
should be interpreted as being included in the scope of the present invention.
1. A magnesium alloy sheet comprising:
3.0 wt% or less (excluding 0 wt%) of Zn, 1.5 wt% or less (excluding 0 wt%) of Ca,
1.0 wt% or less (excluding 0 wt%) of Mn, balance of Mg and inevitable impurities,
for a total of 100 wt%,
wherein, the magnesium alloy sheet further comprises 0.3 wt% or less of Al, based
on 100 wt% of the entire magnesium alloy sheet, and
the magnesium alloy sheet satisfies the following formulas (1) and (2):
[Zn]/[Ca]≤4.0------------ formula (1)
[Zn]+[Ca]>[Mn] formula (2)
[Zn], [Ca], and [Mn] refer to weight percent of each component.
2. The magnesium alloy sheet of Claim 1,
wherein, a maximum texture intensity based on the {0001} plane of the magnesium alloy
sheet is 1 to 4.
3. The magnesium alloy sheet of Claim 1,
wherein, the magnesium alloy sheet has 7 to 10 mm of Limit Dome Height (LDH).
4. The magnesium alloy sheet of Claim 1,
wherein, the magnesium alloy sheet has 170 MPa or more of yield strength.
5. The magnesium alloy sheet of Claim 1,
wherein, the magnesium alloy sheet has 240 MPa or more of tensile strength.
6. The magnesium alloy sheet of Claim 1,
wherein, the magnesium alloy sheet has 20% or more of elongation percentage.
7. The magnesium alloy sheet of Claim 1,
wherein, the magnesium alloy sheet comprises crystal grain having an average particle
size of 1 to 20 µm.
8. The magnesium alloy sheet of Claim 1,
wherein, the magnesium alloy sheet comprises a Mg-Ca based secondary phase, and
the average particle size of the secondary phase is 30 µm or less.
9. The magnesium alloy sheet of Claim 1,
wherein the magnesium alloy sheet comprises 1 to 20 secondary phases per 100 µm2 of the magnesium alloy sheet area.
10. A method of manufacturing a magnesium alloy sheet comprising:
preparing a cast material by casting a molten alloy comprising 3.0 wt% or less (excluding
0 wt%) of Zn, 1.5 wt% or less (excluding 0 wt%) of Ca, 1.0 wt% or less (excluding
0 wt%) of Mn, balance of Mg and inevitable impurities, for a total of 100 wt%;
subjecting the cast material to homogenizing heat treatment;
preparing a rolled material by subjecting the homogenizing heat treated cast material
to hot rolling; and
final annealing the rolled material;
wherein, the molten alloy further comprises 0.3 wt% or less of Al, based on 100 wt%
of the entire molten alloy, and
the magnesium alloy sheet satisfies the following formulas (1) and (2):
[Zn]/[Ca]≤4.0 ------------ formula (1)
[Zn]+ [Ca]>[Mn] formula (2)
[Zn], [Ca], and [Mn] refer to weight percent of each component.
11. The method of Claim 10,
wherein, in the step of final annealing the rolled material,
a temperature range is from 200 to 500°C.
12. The method of Claim 11,
wherein, a step of the final annealing the rolled material is conducted for less than
5 hours (excluding 0 hours).
13. The method of Claim 10,
wherein, in a step of the subjecting the cast material to homogenizing heat treatment;
a temperature range is from 300 to 500°C.
14. The method of Claim 13,
wherein, a step of the subjecting the cast material to homogenizing heat treatment
is conducted for 5 hours to 30 hours.
15. The method of Claim 10,
wherein, in a step of preparing a rolled material by subjecting the homogenizing heat
treated cast material to hot rolling,
a temperature range is from 150 to 400°C.
16. The method of Claim 15,
wherein, the step of preparing a rolled material by subjecting the homogenizing heat
treated cast material to hot rolling,
the cast material is rolled once or twice at a reduction ratio of not more than 40%
(excluding 0%) per rolling.
17. The method of Claim 16,
wherein, the step of preparing a rolled material by subjecting the homogenizing heat
treated cast material to hot rolling,
the cast material is hot-rolled twice or more, and
an intermediate annealing is performed at least once between hot rolling.
18. The method of Claim 17,
the intermediate annealing is performed at a temperature range of 300 to 500 °C
19. The method of Claim 18,
the intermediate annealing is performed for 5 hours or less (excluding 0 hours).