[Technical Field]
[0001] The present disclosure relates to a zinc alloy plated steel sheet having high bending
workability and a method for manufacturing the zinc alloy plated steel sheet.
[Background Art]
[0002] A zinc plating method for suppressing the corrosion of iron by cathodic protection
has high anti-corrosion efficiency and economic feasibility, and thus has been widely
used in manufacturing steel materials having high corrosion resistance. Particularly,
hot-dip zinc plated steel sheets, manufactured by dipping a steel material into molten
zinc to form a plating layer, are obtainable through simple manufacturing processes
and are relatively inexpensive, as compared to electro-zinc plated steel sheets, and
thus, demand therefor has increased in a wide range of industries, such as the automotive
industry, the home appliance industry, and the construction industry.
[0003] When a hot-dip zinc plated steel sheet is exposed to a corrosive environment, zinc
having a lower oxidation-reduction potential than iron undergoes corrosion first,
and thus, corrosion of the steel sheet is suppressed by sacrificial corrosion protection.
Along with this, compact corrosion products are formed on the surface of the steel
sheet as zinc of a plating layer is oxidized, thereby protecting the steel sheet from
the corrosive environment and improving the corrosion resistance of the steel sheet.
[0004] However, air pollution and corrosive environments have increased with industrial
advances, and regulations on resource and energy savings have been tightened. Therefore,
the need to develop a steel material having higher corrosion resistance than existing
zinc plated steel sheets has increased.
[0005] In this regard, research has been variously conducted into techniques for manufacturing
zinc alloy-based plated steel sheets having corrosion resistance improved by adding
elements such as aluminum (Al) and magnesium (Mg) to a zinc plating bath. Techniques
for manufacturing a Zn-Al-Mg-based zinc alloy plated steel sheet, which is representative
of zinc alloy-based plated steel sheets and manufactured by additionally adding magnesium
(Mg) to a Zn-Al plating composition, have been actively researched.
[0006] However, such a Zn-Al-Mg-based zinc alloy plated steel sheet has poor bending workability.
That is, the zinc alloy plated steel sheet includes large amounts of Zn-Al-Mg-based
intermetallic compounds in a plating layer thereof as a result of thermodynamic reaction
between zinc (Zn), aluminum (Al), and magnesium (Mg), and such intermetallic compounds
may cause cracks in the plating layer during a bending process because of high hardness
of the intermetallic compounds, thereby lowering the bending workability of the zinc
alloy plated steel sheet.
[Disclosure]
[Technical Problem]
[0007] Aspects of the present disclosure may provide a zinc alloy plated steel sheet having
high bending workability and a method for manufacturing the zinc alloy plated steel
sheet.
[0008] The present disclosure is not limited to the above-mentioned aspects. Other aspects
of the present disclosure are stated in the following description, and the aspects
of the present disclosure will be clearly understood by those of ordinary skill in
the art through the following description.
[Technical Solution]
[0009] According to an aspect of the present disclosure, a zinc alloy plated steel sheet
may include a base steel sheet and a zinc alloy plating layer, wherein the zinc alloy
plating layer may include a Zn single phase structure as a microstructure and a Zn-Al-Mg-based
intermetallic compound, and the Zn single phase structure may have a degree (f) of
(0001) preferred orientation, expressed by Formula 1 below, within a range of 50%
or greater,

where I
total refers to an integral of all diffraction peaks of the Zn single phase structure when
an X-ray diffraction pattern is measured within a range of 2 theta from 10° to 100°
using a Cu-Kα source, and I
basal refers to an integral of diffraction peaks of the Zn single phase structure relating
to a basal plane.
[0010] According to another aspect of the present disclosure, a method for manufacturing
a zinc alloy plated steel sheet may include: preparing a zinc alloy plating bath including
magnesium (Mg) and aluminum (Al); obtaining a zinc alloy plated steel sheet by dipping
a base steel sheet into the zinc alloy plating bath to plate the base steel sheet;
wiping the zinc alloy plated steel sheet with gas to adjust a plating weight; and
after adjusting the plating weight of the zinc alloy plated steel sheet, cooling the
zinc alloy plated steel sheet by spraying droplets of water or an aqueous solution
onto the zinc alloy plated steel sheet and then using air, wherein when the droplets
are sprayed, a droplet spray start temperature ranges from 405°C to 425°C, a droplet
spray stop temperature ranges from 380°C to 400°C.
[Advantageous Effects]
[0011] According to one of various effects of the present disclosure, an embodiment of the
present disclosure provides a zinc alloy plated steel sheet having high bending workability
as well as high corrosion resistance.
[0012] In addition, according to one of various effects of the present disclosure, the zinc
alloy plated steel sheet of the embodiment has high surface quality.
[0013] In addition, according to one of various effects of the present disclosure, the zinc
alloy plated steel sheet of the embodiment has high scratch resistance.
[Description of Drawings]
[0014]
FIGS. 1A and 1B are views illustrating results of an observation of a surface microstructure
of Inventive Sample 1 and an observation of a surface microstructure of Comparative
Sample 5.
FIGS. 2A and 2B are views illustrating results of an observation of a cross-sectional
microstructure of Inventive Sample 1 and an observation of a cross-sectional microstructure
of Comparative Sample 5.
FIG. 3 is a view illustrating results of X-ray diffractometer (XRD) analysis of Inventive
Sample 1.
[Best Mode]
[0015] Hereinafter, a zinc alloy plated steel sheet having high bending workability will
be described in detail according to an aspect of the present disclosure.
[0016] According to the aspect of the present disclosure, the zinc alloy plated steel sheet
includes a base steel sheet and a zinc alloy plating layer. In the present disclosure,
the base steel sheet is not limited to a particular type. For example, a hot-rolled
steel sheet or a cold-rolled steel sheet commonly used as a base steel sheet of a
zinc alloy plated steel sheet may be used. However, hot-rolled steel sheets have a
large amount of surface oxide scale that lowers plating adhesion and thus plating
quality, and thus a hot-rolled steel sheet from which oxide scale has been previously
removed using an acid solution may be used as the base steel sheet. In addition, the
zinc alloy plating layer may be formed on one or each side of the base steel sheet.
[0017] The zinc alloy plating layer may include, by wt%, aluminum (Al): 0.5% to 3%, magnesium
(Mg): 0.5% to 3%, and the balance of zinc (Zn) and inevitable impurities.
[0018] In the zinc alloy plating layer, magnesium (Mg) reacts with zinc (Zn) and aluminum
(Al) and forms a Zn-Al-Mg-based intermetallic compound, thereby functioning as a key
element improving the corrosion resistance of the zinc alloy plated steel sheet. If
the content of magnesium (Mg) is excessively low, the Zn-Al-Mg-based intermetallic
compound is not present in sufficient amounts in the microstructure of the zinc alloy
plating layer, and thus corrosion resistance may not be sufficiently improved. Therefore,
the amount of magnesium (Mg) in the zinc alloy plating layer may be 0.5 wt% or greater,
preferably 1.0 wt% or greater. However, if the content of magnesium (Mg) is excessively
high, the effect of improving corrosion resistance is saturated, and Mg oxide dross
having a negative effect on platability may be formed in a plating bath. In addition,
the Zn-Al-Mg-based intermetallic compound having high harness may be formed in excessively
large amounts in the microstructure of the zinc alloy plating layer, and thus bending
workability may be lowered. Therefore, the amount of magnesium (Mg) in the zinc alloy
plating layer may be 3 wt% or less, preferably 2.9 wt% or less.
[0019] Aluminum (Al) suppresses the formation of Mg oxide dross and reacts with zinc (Zn)
and magnesium (Mg) to form the Zn-Al-Mg-based intermetallic compound in the zinc alloy
plating layer, thereby functioning as a key element improving the corrosion resistance
of the zinc alloy plated steel sheet. If the content of aluminum (Al) is excessively
low, the formation of Mg dross is not sufficiently suppressed, and the Zn-Al-Mg-based
intermetallic compound is not present in sufficient amounts in the microstructure
of the zinc alloy plating layer, which may result in insufficient improvements in
corrosion resistance. Therefore, the amount of aluminum (Al) in the zinc alloy plating
layer may be 0.5 wt% or greater, preferably 0.6 wt% or greater. However, if the content
of aluminum (Al) is excessively high, the effect of improving corrosion resistance
is saturated, and the durability of plating equipment may be negatively affected because
of a high plating bath temperature. Moreover, the Zn-Al-Mg-based intermetallic compound
having high harness may be formed in excessively large amounts in the microstructure
of the zinc alloy plating layer, and thus bending workability may be lowered. Therefore,
the amount of aluminum (Al) in the zinc alloy plating layer may be 3 wt% or less,
preferably 2.6 wt% or less.
[0020] According to an embodiment, the contents of magnesium (Mg) and aluminum (Al) in the
zinc alloy plating layer may satisfy the following Formula 1. If [Mg]/[Al] is 1.0
or less, scratch resistance may deteriorate, and if [Mg]/[Al] is greater than 4.0,
Mg-based dross may be formed in large amounts in a hot-dip plating bath to lower workability.

where [Mg] and [Al] refer to the weight percentages (wt%) of corresponding elements,
respectively.
[0021] The zinc alloy plating layer may include a Zn single phase structure as a microstructure
and the Zn-Al-Mg-based intermetallic compound. In the present disclosure, the Zn-Al-Mg-based
intermetallic compound is not limited to a particular type. However, for example,
the Zn-Al-Mg-based intermetallic compound may include at least one selected from the
group consisting of a Zn/Al/MgZn
2 ternary eutectic structure, a Zn/MgZn
2 binary eutectic structure, a Zn-Al binary eutectic structure, and an MgZn
2 single phase structure.
[0022] The inventors have conducted in-depth research into improving the bending workability
of zinc alloy plated steel sheets and found that if a Zn single phase structure having
a hexagonal close packing (HCP) structure is grown in a (0001) orientation in the
microstructure of the zinc alloy plating layer, ductility increases owing to easy
slippage, and thus cracks are markedly reduced in a bending process.
[0023] In the present disclosure, to obtain this effect, the degree (f) of (0001) preferred
orientation, expressed by the following formula 1, may preferably be adjusted to be
50% or greater, more preferably 60% or greater.

where I
total refers to the integral of all diffraction peaks of the Zn single phase structure
when an X-ray diffraction pattern is measured within the range of 2 theta from 10°
to 100° using a Cu-Kα source, and I
basal refers to the integral of diffraction peaks of the Zn single phase structure relating
to a basal plane.
[0024] In addition, the inventors have found that if the Zn single phase structure coarsely
formed in the zinc alloy plating layer is refined in size, it is also helpful to reduce
cracking during a bending process.
[0025] To obtain this effect of the present disclosure, the average grain diameter of the
Zn single phase structure may be preferably adjusted to be 15 µm or less, more preferably
12 µm or less, and even more preferably 10 µm or less. The "average grain diameter"
of the Zn single phase structure refers to the average of equivalent circular diameters
of the Zn single phase structure measured by observing a thicknesswise cross-section
of the zinc alloy plating layer. The zinc alloy plated steel sheet of the present
disclosure has high corrosion resistance and bending workability as well.
[0026] According to an embodiment, the zinc alloy plated steel sheet of the present disclosure
may have a good appearance. Specifically, the number of black spots per unit area
may be equal to or less than 0.1/cm
2 on the surface of the zinc alloy plated steel sheet.
[0027] To obtain these effects of the present disclosure, the area fraction of the Zn single
phase structure may preferably be 40% or less (excluding 0%) on the surface of the
zinc alloy plating layer. That is, the appearance of the zinc alloy plated steel sheet
may be improved by maximizing the fraction of the Zn-Al-Mg-based intermetallic compound
present on the surface of the zinc alloy plating layer.
[0028] According to an embodiment, the zinc alloy plated steel sheet of the present disclosure
may also have high scratch resistance.
[0029] According to results of research conducted by the inventors, if the area fractions
of the Zn/MgZn
2 binary eutectic structure and the Zn/Al/MgZn
2 ternary eutectic structure which have a layer structure and are present on the surface
of the zinc alloy plating layer are maximized, scratch resistance may be markedly
improved.
[0030] To obtain this effect of the present disclosure, preferably, the sum of the area
fractions of the Zn/MgZn
2 binary eutectic structure and the Zn/Al/MgZn
2 ternary eutectic structure may be 50% or greater (excluding 100%), and the area fraction
of the MgZn
2 single phase structure may be 10% or less (including 0%). The MgZn
2 single phase structure has high hardness and thus causes cracks during a machining
process, and thus the area fraction of the MgZn
2 single phase structure may be adjusted to be as low as possible.
[0031] The zinc alloy plated steel sheet of the present disclosure may be manufactured by
various methods without limitation. However, for example, when the zinc alloy plating
layer solidifies from a molten state, the zinc alloy plating layer may be cooled by
spraying droplets thereon and then cooled with air to obtain the above-described degree
of preferred orientation and average grain diameter.
[0032] In this case, droplets may be sprayed by a charge spray method to attach the droplets
by electrostatic attraction between the droplets and the zinc alloy plated steel sheet.
This charge spray method may be helpful in forming fine, uniform droplets and reducing
the amount of droplets colliding with and bouncing off the zinc alloy plated steel
sheet after being sprayed on the zinc alloy plated steel sheet, thereby facilitating
rapid cooling of the zinc alloy plating layer from the molten state and having a positive
effect on the growth of the Zn single phase structure in the (0001) orientation and
refinement of the Zn single phase structure.
[0033] The droplets may be droplets of a phosphate aqueous solution capable of rapidly cooling
the zinc alloy plating layer from the molten state through an endothermic reaction
and thus effective in growing the Zn single phase structure in the (0001) orientation
and refining the Zn single phase structure. Examples of the phosphate aqueous solution
may include an aqueous solution of ammonium hydrogen phosphate ((NH
4)
2HPO
4), an aqueous solution of sodium ammonium hydrogen phosphate (NaNH
4HPO
4), an aqueous solution of zinc dihydrogen phosphate (Zn(H
2PO
4)
2), and an aqueous solution of calcium phosphate (Ca
3(PO
4)
2).
[0034] In addition, the content of the phosphate aqueous solution may be 1 wt% to 3 wt%.
If the content of the phosphate aqueous solution is less than 1 wt%, the effect of
the phosphate aqueous solution may not be sufficient. If the content of the phosphate
aqueous solution is greater than 3 wt%, the effect of the phosphate aqueous solution
is saturated, and nozzle clogging may occur in a continuous production process, lowering
productivity.
[0035] In addition, when the droplets may be sprayed at a droplet spray start temperature
of 405°C to 425°C, and more preferably 410°C to 420°C. Here, the term "droplet spray
start temperature" refers to a surface temperature of the zinc alloy plated steel
sheet at the start time of droplet spraying. If the droplet spray start temperature
is less than 405°C, solidification of the Zn single phase structure may have already
started, and thus black spots may be formed on the surface of the zinc alloy plated
steel sheet. Conversely, if the droplet spray start temperature is greater than 425°C,
droplets may not effectively undergo an endothermic reaction, and thus it may be difficult
to obtain an intended structure.
[0036] In addition, the droplets may be sprayed at a droplet spray stop temperature of 380°C
to 400°C, and more preferably 390°C to 400°C. Here, the term "droplet spray stop temperature"
refers to a surface temperature of the zinc alloy plated steel sheet at a point in
time at which spraying of droplets stops. If the droplet spray stop temperature is
greater than 400°C, an endothermic reaction by the droplets may occur ineffectively,
and thus it may be difficult to obtain an intended structure. Conversely, if the droplet
spray stop temperature is less than 380°C, a Mg
2Zn
11 phase may be formed due to over cooling while the Zn/MgZn
2 binary eutectic phase and the Zn/Al/MgZn
2 ternary phase start to solidify, and thus many black spots may be formed, decreasing
the degree of (0001) preferred orientation of the Zn single phase structure.
[0037] In addition, the difference between the droplet spray start temperature and the droplet
spray stop temperature may be 15°C or greater. If the difference is less than 15°C,
the droplets may not undergo an effective endothermic reaction, and thus it may be
difficult to obtain an intended structure.
[0038] In addition, the droplets may be sprayed in an amount of 50 g/m
2 to 100 g/m
2. If the spraying amount of the droplets is less than 50 g/m
2, the effect of the droplets may be insufficient, and if the spraying amount of the
droplets is greater than 100 g/m
2, the effect of the droplets may be saturated.
[Mode for Invention]
[0039] Hereinafter, the present disclosure will be described more specifically through examples.
However, the following examples should be considered in a descriptive sense only and
not for purpose of limitation. The scope of the present invention is defined by the
appended claims, and modifications and variations reasonably made therefrom.
(Example 1)
[0040] Low carbon cold-rolled steel sheets each having a thickness of 0.8 mm, a width of
100 mm, and a length of 200 mm were prepared as base steel sheets for plating test
samples, and then foreign substances such as rolling oil were removed from the surfaces
of the base steel sheets by dipping the base steel sheets into acetone and washing
the base steel sheets with ultrasonic waves. Thereafter, a 750°C reducing atmosphere
heat treatment commonly performed to guarantee mechanical characteristics of steel
sheets in the hot-dipping plating field was performed on the base steel sheets, and
then the base steel sheets were dipped into plating baths (bath temperature: 460°C)
having compositions shown in Table 1 below to fabricate zinc alloy plated steel sheets.
Thereafter, each of the zinc alloy plated steel sheets was wiped with gas to adjust
a plating weight to be 70 g/m
2 on each side. Then, the zinc alloy plated steel sheets were cooled under the conditions
shown in Table 1 below and were cooled with air. Although not shown in Table 1 below,
Comparative Sample 5 was prepared by performing a gas wiping process on a zinc alloy
plated steel sheet fabricated using the same plating bath as that used to fabricate
Inventive Sample 1 to adjust a plating weight to be 70 g/m
2 on each side, and then cooling the zinc alloy plated steel sheet using a general
cooling device at an average cooling rate of 12°C/sec until the plating layer of the
zinc alloy plated steel sheet was completely solidified (at about 300°C or less).
[0041] Then, the microstructures of the fabricated zinc alloy plated steel sheets were observed
using an FE-SEM (SUPRA-55VP, Zeiss) as illustrated in FIGS. 1 and 2, and the average
grain diameter of a Zn single phase structure of each of the zinc alloy plated steel
sheets was measured as shown in Table 2 below.
[0042] Thereafter, the degree (f) of (0001) preferred orientation of the Zn single phase
structure was measured using the following Formula 1, and results thereof are shown
in Table 2 below.

where I
total refers to the integral of all diffraction peaks of the Zn single phase structure
when an X-ray diffraction pattern was measured within the range of 2 theta from 10°
to 100° using a Cu-Kα source, and I
basal refers to the integral of diffraction peaks of the Zn single phase structure relating
to a basal plane.
[0043] Thereafter, the bending workability of each of the zinc alloy plated steel sheets
was evaluated, and results thereof are shown in Table 2 below.
[0044] Corrosion resistance was evaluated as follows.
[0045] A salt spray test (based on KS-C-0223) was performed on each of the zinc alloy plated
steel sheets to facilitate corrosion, and then the time taken until the area fraction
of red rust on the surface of each plating layer was 5% was measured.
[0046] Bending workability was evaluated as follows.
[0047] 3T bending was performed on each of the zinc alloy plated steel sheets, and a 1-mm
length of the apex of each bent portion was observed using an SEM to measure the area
fraction of bending cracks using an image analysis system.
[Table 1]
| No. |
Composition of plating bath (wt%) |
Droplet spray start temperature (°C) |
Droplet spray stop temperature (°C) |
Droplets |
Spraying amount (g/m2) |
Notes |
| Al |
Mg |
| 1 |
1.6 |
1.6 |
410 |
390 |
Aqueous solution of ammonium hydrogen phosphate, 2 wt% |
70 |
*IS 1 |
| 2 |
1.6 |
1.6 |
420 |
400 |
Aqueous solution of ammonium hydrogen phosphate, 2 wt% |
70 |
IS 2 |
| 3 |
1.6 |
1.6 |
430 |
400 |
Aqueous solution of ammonium hydrogen phosphate, 2 wt% |
70 |
**CS 1 |
| 4 |
1.6 |
1.6 |
400 |
390 |
Aqueous solution of ammonium hydrogen phosphate, 2 wt% |
70 |
CS 2 |
| 5 |
1.6 |
1.6 |
420 |
405 |
Aqueous solution of ammonium hydrogen phosphate, 2 wt% |
70 |
CS 3 |
| 6 |
1.6 |
1.6 |
410 |
375 |
Aqueous solution of ammonium hydrogen phosphate, 2 wt% |
70 |
CS 4 |
| *IS: Inventive Sample, **CS: Comparative Sample |
[Table 2]
| No. |
Average grain diameter of Zn single phase structure (µm) |
f(%) |
Red rust occurrence time (h) |
Area fraction of bending cracks (%) |
Notes |
| 1 |
8 |
63 |
650 |
8 |
*IS 1 |
| 2 |
10 |
62 |
645 |
9 |
IS 2 |
| 3 |
12 |
49 |
640 |
25 |
**CS 1 |
| 4 |
14 |
47 |
630 |
38 |
CS 2 |
| 5 |
15 |
46 |
620 |
40 |
CS 3 |
| 6 |
16 |
44 |
610 |
42 |
CS 4 |
| 7 |
18 |
42 |
600 |
45 |
CS 5 |
| *IS: Inventive Sample, **CS: Comparative Sample |
[0048] Referring to Table 2, Inventive Samples 1 and 2 satisfying conditions proposed in
the present disclosure had high bending workability.
[0049] However, although Comparative Samples 1 to 5 had high corrosion resistance, Comparative
Samples 1 to 5 had poor bending workability because the (f) values thereof were less
than 50%.
[0050] FIG. 1A and 1B are views illustrating results of an observation of a surface microstructure
of Inventive Sample 1 of the present disclosure and an observation of a surface microstructure
of Comparative Sample 5, and FIGS. 2A and 2B are views illustrating results of an
observation of a cross-sectional microstructure of Inventive Sample 1 of the present
disclosure and an observation of a cross-sectional microstructure of Comparative Sample
5.
[0051] FIG. 3 is a view illustrating results of X-ray diffractometer (XRD) analysis of Inventive
Sample 1. In FIG. 1, peaks denoted with "○" and "●" are all diffraction peaks of the
Zn single phase structure, and the peaks denoted with "○" are diffraction peaks of
the Zn single phase structure relating to a basal plane.
(Example 2)
[0052] Low carbon cold-rolled steel sheets each having a thickness of 0.8 mm, a width of
100 mm, and a length of 200 mm were prepared as base steel sheets for plating test
samples, and then foreign substances such as rolling oil were removed from the surfaces
of the base steel sheets by dipping the base steel sheets into acetone and washing
the base steel sheets with ultrasonic waves. Thereafter, a 750°C reducing atmosphere
heat treatment commonly performed to guarantee mechanical characteristics of steel
sheets in the hot-dipping plating field was performed on the base steel sheets, and
then the base steel sheets were dipped into plating baths having compositions shown
in Table 3 below to fabricate zinc alloy plated steel sheets. Thereafter, each of
the zinc alloy plated steel sheets was wiped with gas to adjust a plating weight to
be 70 g/m
2 on each side. Then, the zinc alloy plated steel sheets were cooled under the same
conditions as Inventive Sample 1 of Example 1.
[0053] Thereafter, the fractions of microstructures observed on the surface of each of the
zinc alloy plated steel sheets were measured, and the number of black spots on the
surface of each of the zinc alloy plated steel sheets was measured. Results thereof
are shown in Tables 3 and 4.
[0054] Thereafter, a friction test (linear friction test) was performed by rubbing the surface
of each of the zinc alloy plated steel sheets 20 times with a tool head at a constant
pressure. In the friction test, a target load was 333.3 kgf, a pressure was 3.736
MPa, the tool head traveled 200 mm per rub, and the speed of the tool head was 20
mm/s.
[0055] After the friction test, a stripping test was performed on each of the zinc alloy
plated steel sheets. Specifically, cellophane adhesive tape (NB-1 by Ichiban) was
attached to a bent portion of each of the zinc alloy plated steel sheets subjected
to a 10R bending process, and then the cellophane tape was momentarily separated.
Then, the number of plating layer defects was measured using an optical microscope
(magnification: 50 times). Results of the measurement were evaluated as "○" when the
number of plating layer defects was 5/m
2 or less, and "X" when the number of plating layer defects was greater than 5/m
2. Evaluation results are shown in Table 4 below.
[0056] In addition, after the friction test, each of the zinc alloy plated steel sheets
was inserted into a salt spray tester, and the time taken until the occurrence of
red rust was measured according to international standard ASTM B117-11. In that time,
a 5% salt solution (35°C, pH 6.8) was sprayed at a rate of 2 ml/80 cm
2 per hour. When the time taken until red rust was present on a sample was 500 hours
or greater, the sample was evaluated as "○", and when the time taken until red rust
was present on a sample was less than 500, the sample was evaluated as "X." Results
of the evaluation are shown in Table 4 below.
[Table 3]
| No. |
Alloy composition (wt%) |
Area fractions of surface structures (area%) |
Notes |
| Al |
Mg |
Mg/Al |
Zn |
Zn/MgZn2 |
Zn/Al/MgZn2 |
MgZn2 |
Zn/Al |
Zn/Al/MgZn2 + Zn/MgZn2 |
| 1 |
0.6 |
2.3 |
3.83 |
28 |
41 |
31 |
0 |
0 |
72 |
*IS A |
| 2 |
1.5 |
2.8 |
1.87 |
20 |
57 |
21 |
1 |
1 |
78 |
IS B |
| 3 |
2 |
2.9 |
1.45 |
8 |
63 |
28 |
1 |
0 |
91 |
IS C |
| 4 |
2.2 |
2.7 |
1.23 |
4 |
58 |
34 |
2 |
2 |
92 |
IS D |
| 5 |
2.6 |
2.9 |
1.12 |
4 |
39 |
51 |
3 |
3 |
90 |
IS E |
| 6 |
0 |
0 |
- |
100 |
0 |
0 |
0 |
0 |
0 |
**CS A |
| 7 |
1.4 |
1 |
0.71 |
82 |
7 |
11 |
0 |
0 |
18 |
CS B |
| 8 |
2.5 |
1.2 |
0.48 |
6 |
21 |
26 |
46 |
1 |
47 |
CS C |
| 9 |
5 |
0 |
0.00 |
76 |
0 |
0 |
0 |
24 |
0 |
CS D |
| 10 |
5 |
1 |
0.20 |
59 |
9 |
11 |
0 |
21 |
20 |
CS E |
| 11 |
8 |
3 |
0.38 |
13 |
7 |
13 |
18 |
49 |
20 |
CS F |
| 12 |
55 |
0 |
0.00 |
14 |
0 |
0 |
0 |
86 |
0 |
CS G |
| Here, surface structures refer to microstructures observed on the surfaces of zinc
alloy plating layers. |
| *IS: Inventive Sample, **CS: Comparative Sample |
[Table 4]
| No. |
Number of black spots (/cm2) |
Results of stripping test after friction test |
Results of salt spray test after friction test |
Notes |
| Number of defects (/m2) |
Evaluation results |
Separated area (%) |
Evaluation results |
| 1 |
0.05 |
3 |
○ |
520 |
○ |
*IS A |
| 2 |
0.08 |
2 |
○ |
550 |
○ |
IS B |
| 3 |
0.04 |
4 |
○ |
600 |
○ |
IS C |
| 4 |
0.08 |
3 |
○ |
650 |
○ |
IS D |
| 5 |
0.04 |
2 |
○ |
580 |
○ |
IS E |
| 6 |
1.2 |
2 |
○ |
120 |
X |
**CS A |
| 7 |
0.8 |
3 |
○ |
230 |
X |
CS B |
| 8 |
0.05 |
23 |
X |
620 |
○ |
CS C |
| 9 |
1.1 |
3 |
○ |
350 |
X |
CS D |
| 10 |
0.6 |
2 |
○ |
420 |
X |
CS E |
| 11 |
0.06 |
15 |
X |
650 |
○ |
CS F |
| 12 |
0.05 |
11 |
X |
200 |
X |
CS G |
| *IS: Inventive Sample, **CS: Comparative Sample |
[0057] Referring to Table 4, Inventive Samples A to E satisfying conditions proposed in
the present disclosure had good appearance and high scratch resistance.
[0058] However, each of Comparative Samples A, B, D, and E had poor appearance because the
area fraction of a Zn single phase structure present on the surface of a plating layer
was excessively high, and each of Comparative Samples A to G had poor scratch resistance
because the area fractions of a Zn/MgZn
2 binary eutectic structure and a Zn/Al/MgZn
2 ternary eutectic structure are excessively low.
1. A zinc alloy plated steel sheet comprising a base steel sheet and a zinc alloy plating
layer,
wherein the zinc alloy plating layer comprises a Zn single phase structure as a microstructure
and a Zn-Al-Mg-based intermetallic compound, and
the Zn single phase structure has a degree (f) of (0001) preferred orientation, expressed
by Formula 1 below, within a range of 50% or greater,

where I
total refers to an integral of all diffraction peaks of the Zn single phase structure when
an X-ray diffraction pattern is measured within a range of 2 theta from 10° to 100°
using a Cu-Kα source, and I
basal refers to an integral of diffraction peaks of the Zn single phase structure relating
to a basal plane.
2. The zinc alloy plated steel sheet of claim 1, wherein the Zn single phase structure
has a degree (f) of (0001) preferred orientation, expressed by Formula 1, within a
range of 60% or greater.
3. The zinc alloy plated steel sheet of claim 1, wherein the Zn-Al-Mg-based intermetallic
compound comprises at least one selected from the group consisting of a Zn/MgZn2 binary eutectic structure, a Zn/Al binary eutectic structure, an MgZn2 single phase structure, and a Zn/Al/MgZn2 ternary eutectic structure.
4. The zinc alloy plated steel sheet of claim 1, wherein an area fraction of the Zn single
phase structure on a surface of the zinc alloy plating layer is 40% or less (excluding
0%).
5. The zinc alloy plated steel sheet of claim 1, wherein a total area fraction of a Zn/MgZn2 binary eutectic structure and a Zn/Al/MgZn2 ternary eutectic structure is 50% or greater (excluding 100%) on a surface of the
zinc alloy plating layer.
6. The zinc alloy plated steel sheet of claim 1, wherein an area fraction of an MgZn2 single phase structure on a surface of the zinc alloy plating layer is 10% or less
(excluding 0%).
7. The zinc alloy plated steel sheet of claim 1, wherein an average grain diameter of
the Zn single phase structure observed on a cross-section of the zinc alloy plating
layer taken in a sheet thickness direction is 15 µm or less (excluding 0 µm).
8. The zinc alloy plated steel sheet of claim 1, wherein the zinc alloy plating layer
comprises, by wt%, aluminum (Al): 0.5% to 3%, magnesium (Mg): 0.5% to 3%, and a balance
of zinc (Zn) and inevitable impurities.
9. The zinc alloy plated steel sheet of claim 1, wherein the zinc alloy plating layer
satisfies Formula 1 below:

where [Mg] and [Al] refer to weight percentages (wt%) of corresponding elements,
respectively.
10. The zinc alloy plated steel sheet of claim 1, wherein a number of black spots per
unit area is 0.1/cm2 or less on a surface of the zinc alloy plated steel sheet.
11. A method for manufacturing a zinc alloy plated steel sheet, the method comprising:
preparing a zinc alloy plating bath comprising magnesium (Mg) and aluminum (Al);
obtaining a zinc alloy plated steel sheet by dipping a base steel sheet into the zinc
alloy plating bath to plate the base steel sheet;
wiping the zinc alloy plated steel sheet with gas to adjust a plating weight; and
after adjusting the plating weight of the zinc alloy plated steel sheet, cooling the
zinc alloy plated steel sheet by spraying droplets of water or an aqueous solution
onto the zinc alloy plated steel sheet and then using air,
wherein when the droplets are sprayed, a droplet spray start temperature ranges from
405°C to 425°C, a droplet spray stop temperature ranges from 380°C to 400°C.
12. The method of claim 11, wherein when the droplets are sprayed, a difference between
the droplet spray start temperature and the droplet spray stop temperature is 15°C
or greater.
13. The method of claim 11, wherein the droplets are sprayed by a charge spray method
to attach the droplets by electrostatic attraction between the droplets and the zinc
alloy plated steel sheet.
14. The method of claim 11, wherein the droplets are sprayed in an amount of 50 g/m2 to 100 g/m2.
15. The method of claim 11, wherein the aqueous solution is a phosphate aqueous solution.
16. The method of claim 15, wherein the phosphate aqueous solution comprises at least
one selected from the group consisting of an aqueous solution of ammonium hydrogen
phosphate ((NH4)2HPO4), an aqueous solution of sodium ammonium hydrogen phosphate (NaNH4HPO4), an aqueous solution of zinc dihydrogen phosphate (Zn(H2PO4)2), and an aqueous solution of calcium phosphate (Ca3(PO4)2).
17. The method of claim 15, wherein the phosphate aqueous solution has a concentration
of 0.5 wt% to 5 wt%.
18. The method of claim 11, wherein the zinc alloy plating bath comprises, by wt%, aluminum
(Al): 0.5% to 3%, magnesium (Mg): 0.5% to 3%, and a balance of zinc (Zn) and inevitable
impurities.