Technical Field
[0001] The present invention relates to a medium-entropy alloy (MEA) having excellent cryogenic
mechanical properties, in which inexpensive Fe is included in an amount of 50 at%
or more to thus exhibit high price competitiveness, and moreover, in which face-centered
cubic (FCC) and body-centered cubic (BCC) phase stability may be adjusted through
control of alloying elements to thus cause deformation-induced phase transformation
during cryogenic deformation, thereby realizing excellent cryogenic mechanical properties.
Background Art
[0002] A high-entropy alloy (HEA) is a multielement alloy obtained by alloying five or more
constituent elements at a similar ratio without a major element of the alloy. A high-entropy
alloy is a metal material having a single-phase structure, such as a face-centered
cubic (FCC) phase or a body-centered cubic (BCC) phase, without forming intermetallic
compounds or intermediate phases, due to high entropy of mixing in the alloy.
[0003] In particular, a Co-Cr-Fe-Mn-Ni-based high-entropy alloy has excellent cryogenic
properties, high fracture toughness and high corrosion resistance, and is thus receiving
attention as a material suitable for use in extreme environments.
[0004] Two important factors in designing such a high-entropy alloy are the composition
ratio of the constituent elements of the alloy and the configurational entropy of
the alloy system.
[0005] Here, the composition ratio of the high-entropy alloy is discussed first. A high-entropy
alloy has to be composed of at least five elements, and the fraction of each of the
constituent elements of the alloy is set to the range of 5 to 35 at%. Furthermore,
when another element is added in the production of a high-entropy alloy, in addition
to the main alloying elements, the amount thereof should be 5 at% or less.
[0006] Also, alloys are typically divided into high-entropy alloys, medium-entropy alloys
(MEAs), and low-entropy alloys (LEAs), depending on the configurational entropy (ΔS
conf) of the composition of alloying elements, and are classified according to the conditions
of Equation 2 below based on the configurational entropy value determined by Equation
1 below.

(R: Gas constant, X
i: mole fraction of i element, n: number of constituent elements)

[0007] For a Co
20Cr
20Fe
20Mn
20Ni
20 (at%) alloy, which is a representative cryogenic FCC-based high-entropy alloy, the
alloying elements that are added are expensive, resulting in low price competitiveness.
Accordingly, despite the excellent cryogenic properties thereof, the above alloy makes
it difficult to serve as a replacement for existing steel materials in marine plants,
LNG container materials, cryogenic tanks, and ship/marine materials.
[0008] Therefore, the industrialization of high-entropy alloys is essentially required to
ensure price competitiveness through control of alloying elements and also to realize
excellent cryogenic properties.
[Citation List]
Disclosure
Technical Problem
[0011] Accordingly, an objective of the present invention is to provide a medium-entropy
alloy, which is capable of exhibiting superior mechanical properties by causing deformation-induced
phase transformation at cryogenic temperatures, as well as ensuring price competitiveness
by developing an alloy including reduced amounts of expensive alloying elements, in
lieu of a conventional Co-Cr-Fe-Mn-Ni-based alloy.
Technical Solution
[0012] In order to accomplish the above objective, the present invention provides a medium-entropy
alloy, comprising 6 to 15 at% of Cr, 50 to 64 at% of Fe, 13 to 25 at% of Co, 13 to
25 at% of Ni, and the remainder of inevitable impurities.
[0013] Moreover, the medium-entropy alloy according to an embodiment of the present invention
includes a metastable FCC phase at room temperature and causes deformation-induced
phase transformation from the metastable FCC phase into a BCC phase upon cryogenic
deformation, and is thus improved in mechanical properties.
Advantageous Effects
[0014] According to the present invention, a medium-entropy alloy is configured such that
the amount of Fe, which is an inexpensive alloying element, is increased to the range
of 50 to 64 at%, thus reducing the amounts of expensive Co, Cr, and Ni elements that
are added, thereby ensuring price competitiveness, and moreover, the medium-entropy
alloy has superior properties including tensile strength of 1024 MPa or more and elongation
of 47% or more at a cryogenic temperature (77 K).
[0015] Moreover, according to an embodiment of the present invention, the medium-entropy
alloy includes a metastable FCC phase at room temperature (298 K) and causes deformation-induced
phase transformation from the metastable FCC phase into a BCC phase upon deformation
at a cryogenic temperature to thus exhibit strengthening effects, ultimately obtaining
further improved cryogenic mechanical properties.
Description of Drawings
[0016]
FIG. 1 shows the results of measurement of X-ray diffraction (XRD) of Co-Cr-Fe-Ni-based
medium-entropy alloys of Comparative Examples 1 and 2 and Examples 1 to 4 according
to the present invention;
FIG. 2 shows the results of tensile testing at room temperature (298 K) of the Co-Cr-Fe-Ni-based
medium-entropy alloys of Comparative Examples 1 and 2 and Examples 1 to 4 according
to the present invention;
FIG. 3 shows the results of tensile testing at a cryogenic temperature (77 K) of the
Co-Cr-Fe-Ni-based medium-entropy alloys of Comparative Examples 1 and 2 and Examples
1 to 4 according to the present invention; and
FIG. 4 shows the analytical results of electron backscatter diffraction (EBSD) for
phase transformation upon deformation at room temperature and at a cryogenic temperature
of the Co-Cr-Fe-Ni-based medium-entropy alloy of Example 3 according to the present
invention.
Best Mode
[0017] Hereinafter, a detailed description will be given below of preferred embodiments
of the present invention with reference to the appended drawings, but the present
invention is not limited to the following examples. Accordingly, those skilled in
the art will appreciate that various modifications are possible, without departing
from the spirit of the invention.
[0018] The present inventors have performed thorough study in order to obtain excellent
mechanical properties in cryogenic environments while increasing price competitiveness
of high-entropy alloys having superior mechanical properties in cryogenic environments,
and thus have ascertained that the amount of Fe, which is an inexpensive element,
is remarkably increased to the range of 50 to 64 at% compared to conventional high-entropy
alloys, and the amounts of alloying elements other than Fe are adjusted, whereby deformation-induced
phase transformation may occur during deformation due to changes in FCC and BCC phase
stability, resulting in excellent cryogenic mechanical properties.
[0019] In particular, the present inventors have revealed that when an alloy is designed
so as to include an FCC phase in a metastable state at room temperature, deformation-induced
phase transformation from the FCC phase in a metastable state into a BCC phase may
occur during deformation in a cryogenic environment, thereby further improving cryogenic
mechanical properties, which culminates in the present invention.
[0020] In the present invention, when the phase in a metastable state is transformed into
a phase in a stable state at the corresponding temperature through deformation-induced
phase transformation during plastic deformation, it is judged to be a metastable phase.
All of these phases are defined as a metastable phase.
[0021] The medium-entropy alloy according to the present invention has an alloy composition
comprising 6 to 15 at% of Cr, 50 to 64 at% of Fe, 13 to 25 at% of Co, 13 to 25 at%
of Ni, and the remainder of inevitable impurities.
[0022] Furthermore, the medium-entropy alloy according to the present invention includes
a metastable FCC at room temperature, and enables occurrence of deformation-induced
phase transformation from the metastable FCC phase into a BCC phase upon deformation.
[0023] If the amount of chromium (Cr) is less than 6 at%, the FCC phase is stabilized. On
the other hand, if the amount thereof exceeds 15 at%, the BCC phase is stabilized.
Hence, the amount of Cr preferably falls in the range of 6 to 15 at%. Also, since
the formation of the metastable FCC phase is more favorable in terms of improving
cryogenic mechanical properties, the amount of chromium (Cr) more preferably falls
in the range of 7.5 to 12.5 at%.
[0024] If the amount of iron (Fe) is less than 50 at%, the FCC phase is stabilized. On the
other hand, if the amount thereof exceeds 64 at%, the BCC phase is stabilized. Hence,
the amount of Fe preferably falls in the range of 50 to 64 at%. Since the formation
of the metastable FCC phase is more favorable in terms of improving cryogenic mechanical
properties, the amount of iron (Fe) more preferably falls in the range of 55 to 62.5
at%.
[0025] If the amount of cobalt (Co) is less than 13 at%, the FCC phase is stabilized. On
the other hand, if the amount thereof exceeds 25 at%, the BCC phase is stabilized.
Hence, the amount of Co preferably falls in the range of 13 to 25 at%.
[0026] If the amount of nickel (Ni) is less than 13 at%, the BCC phase is stabilized. On
the other hand, if the amount thereof exceeds 25 at%, the FCC phase is stabilized.
Hence, the amount of Ni preferably falls in the range of 13 to 25 at%.
[0027] If the amount of at least one selected from among molybdenum (Mo) and aluminum (Al),
which is a component that may substitute for cobalt (Co), is less than 13 at%, the
FCC phase is stabilized. On the other hand, if the amount thereof exceeds 25 at%,
the BCC phase is stabilized. Hence, the amount thereof preferably falls in the range
of 13 to 25 at%.
[0028] If the amount of manganese (Mn), which is a component that may substitute for nickel
(Ni), is less than 13 at%, the BCC phase is stabilized. On the other hand, if the
amount thereof exceeds 25 at%, the FCC phase is stabilized. Hence, the amount thereof
preferably falls in the range of 13 to 25 at%.
[0029] In general, an interstitial element such as C or N in a metal alloy is subjected
to interstitial solid solution in the metal matrix to thus enhance the strength of
the alloy due to solid-solution strengthening effects during metal deformation. When
at least one element of C and N is added in an amount of 1 at% or more based on the
total at% of the alloy, the FCC phase is stabilized. In order to utilize the effect
of deformation-induced phase transformation by inducing the metastable FCC phase,
it is preferred that the above element be added in an amount of less than 1 at%.
[0030] The inevitable impurities are components other than the above alloying elements and
are unavoidable components that are inevitably incorporated into the alloying elements
or during the production process.
[0031] The medium-entropy alloy may be composed of a metastable FCC phase or a combination
of a metastable FCC phase and a BCC phase at room temperature. Here, it is preferred
that the fraction of the metastable FCC phase be high in the interests of improvements
in tensile strength and elongation. The fraction of the metastable FCC phase is preferably
50% or more. However, the fraction of the metastable FCC phase is not necessarily
50% or more.
[0032] Also, the medium-entropy alloy may have tensile strength of 500 MPa or more and elongation
of 50% or more at room temperature (298 K).
[0033] Also, the medium-entropy alloy may have tensile strength of 1000 MPa or more and
elongation of 40% or more at a cryogenic temperature (77 K).
[Examples 1 to 4]
Production of medium-entropy alloy
[0034] First, Co, Cr, Fe, and Ni metals having purity of 99.9% or more were prepared.
[0035] The metals thus prepared were weighed in the mixing fractions shown in Table 1 below.
[Table 1]
|
Metal mixing fraction (at%) |
Co |
Cr |
Fe |
Ni |
Example 1 |
17.50 |
10.00 |
55.00 |
17.50 |
Example 2 |
16.25 |
10.00 |
57.50 |
16.25 |
Example 3 |
15.00 |
10.00 |
60.00 |
15.00 |
Example 4 |
13.75 |
10.00 |
62.50 |
13.75 |
[0036] The metals prepared in the above fractions were placed in a crucible, heated to 1550°C
and thus melted, and then cast into 150 g of an alloy ingot having a cuboid shape
having a width of 33 mm, a length of 80 mm, and a thickness of 7.8 mm, using a mold.
[0037] In order to remove the oxide formed on the surface of the cast alloy, surface grinding
was performed. The thickness of the ground ingot was 7 mm.
[0038] The surface-ground ingot having a thickness of 7 mm was subjected to homogenization
heat treatment at 1100°C for 6 hr and then cold rolling to a thickness from 7 mm to
1.5 mm.
[0039] Furthermore, the cold-rolled alloy plate was annealed at 800°C for 10 min.
[Comparative Examples 1 and 2]
Production of alloy for Comparative Examples
[0040] The alloys of Comparative Examples were manufactured in the same manner as in Examples
using the components in the amounts shown in Table 2 below.
[Table 2]
|
Metal mixing fraction (at%) |
Co |
Cr |
Fe |
Ni |
Comparative Example 1 |
14.50 |
5.00 |
66.00 |
14.50 |
Comparative Example 2 |
12.50 |
10.00 |
65.00 |
12.50 |
[0041] The alloy ingot was cast in the same manner as in Examples, followed by homogenization
heat treatment at 1100°C for 6 hr and then cold rolling to a thickness from 7 mm to
1.5 mm in the same manner as in Examples.
[0042] Furthermore, the cold-rolled alloy plate was annealed at 800°C for 10 min in the
same manner as in Examples.
Component analysis results
[0043] The actual components of the alloys manufactured in Comparative Examples 1 and 2
and Examples 1 to 4 after annealing treatment were analyzed using EDS. The results
are shown in Table 3 below.
[Table 3]
|
EDS analysis composition (at%) |
Co |
Cr |
Fe |
Ni |
Comparative Example 1 |
14.34 |
5.10 |
66.29 |
14.27 |
Example 1 |
17.37 |
10.52 |
55.58 |
16.53 |
Example 2 |
16.16 |
10.21 |
57.41 |
16.22 |
Example 3 |
14.54 |
10.68 |
60.89 |
13.89 |
Example 4 |
13.55 |
10.27 |
62.55 |
13.63 |
Comparative Example 2 |
12.23 |
10.81 |
65.31 |
11.65 |
[0044] As is apparent from Table 3, the actual composition falls slightly out of the range
of the initial metal mixing fractions, but may be regarded as almost the same level
considering the purity of metals and impurities which may be incorporated during the
production process. All of Examples fell in the composition range of the medium-entropy
alloy according to the present invention, comprising 6 to 15 at% of Cr, 50 to 64 at%
of Fe, 13 to 25 at% of Co, and 13 to 25 at% of Ni.
XRD analysis results
[0045] FIG. 1 shows the results of XRD measurement at room temperature of the annealed alloys
of Comparative Examples 1 and 2 and Examples 1 to 4.
[0046] XRD measurement was performed after grinding in the order of sandpaper Nos. 600,
800 and 1200 and then electrolytic etching in 8% perchloric acid in order to minimize
phase transformation due to deformation during grinding of a test specimen.
[0047] As shown in FIG. 1, Comparative Example 1 was composed of the BCC phase, Examples
1 to 4 were composed mainly of the metastable FCC phase, and Comparative Example 2
was composed mainly of the BCC phase and included a small amount of the FCC phase.
[0048] Specifically, when the amount of Fe was increased and the amounts of Co and Ni were
decreased, the stability of the FCC phase was deteriorated, and consequently the metastable
FCC phase was formed in Examples 1 to 4. In Comparative Examples 1 and 2, in which
Fe was added in an amount of 65 at% or more, the FCC phase was no longer in the metastable
state but became unstable, and the BCC phase was relatively stabilized.
Tensile test results
[0049] The results of tensile testing at room temperature (298 K) and at a cryogenic temperature
(77 K) of the annealed alloys of Comparative Examples 1 and 2 and Examples 1 to 4
according to the present invention are shown in FIGS. 2 and 3 and Table 4 below.
[0050] FIGS. 2 and 3 are graphs showing the results of tensile testing at room temperature
and at a cryogenic temperature, respectively, in which the horizontal axis designates
the engineering strain and the vertical axis designates the engineering stress. Based
on the graphs of the test results, the results of analysis of physical properties
such as yield strength, tensile strength and elongation of Comparative Examples and
Examples 1 to 4 are given in Table 4 below.
[Table 4]
Test specimen |
Room temperature |
Cryogenic temperature (77 K) |
Yield strength (MPa) |
Tensile strength (MPa) |
Elongation (%) |
Yield strength (MPa) |
Tensile strength (MPa) |
Elongation (%) |
Comparative Example 1 |
850 |
975 |
24 |
1336 |
1455 |
33 |
Example 1 |
280 |
550 |
68 |
615 |
1024 |
126 |
Example 2 |
274 |
568 |
86 |
543 |
1164 |
118 |
Example 3 |
226 |
534 |
98 |
526 |
1508 |
82 |
Example 4 |
228 |
787 |
67 |
620 |
1649 |
47 |
Comparative Example 2 |
579 |
996 |
26 |
1110 |
1516 |
30 |
[0051] As is apparent from FIGS. 2 and 3 and Table 3, the tensile properties at room temperature
of the medium-entropy alloys of Examples 1 to 4 according to the present invention
exhibited yield strength of 226 to 280 MPa, tensile strength of 534 to 787 MPa, and
elongation of 67 to 98%.
[0052] Furthermore, excellent tensile properties at a cryogenic temperature, such as yield
strength of 526 to 620 MPa, tensile strength of 1024 to 1649 MPa, and elongation of
47 to 126%, were manifested.
[0053] In contrast, the tensile properties at room temperature of the medium-entropy alloys
of Comparative Examples 1 and 2 were as follows: since the initial crystal structure
was mostly composed of a BCC structure, there were neither strengthening effects nor
elongation enhancement effects due to deformation-induced phase transformation between
tensile deformation at room temperature and tensile deformation at a cryogenic temperature,
and tensile yield strength and tensile strength were high at room temperature and
at a cryogenic temperature due to the BCC structure, but elongation was low, resulting
in brittleness.
[0054] In particular, the alloy of Example 3, including a large amount of the FCC phase
in the metastable state, manifested excellent tensile properties at a cryogenic temperature,
such as yield strength of 526 MPa, tensile strength of 1508 MPa, and elongation of
82%, which were not previously reported.
[0055] Additionally, in the medium-entropy alloy of the present invention, even when at
least one of Mo and Al substituting for Co was added in the same amount as Co under
the condition that the amounts of Cr and Fe were maintained, deformation-induced phase
transformation occurred during deformation, as was expected in the present invention,
whereby ductility and stiffness were observed at a cryogenic temperature.
[0056] Also, in the medium-entropy alloy of the present invention, even when Mn substituting
for Ni was added in the same amount as Ni under the condition that the amounts of
Cr and Fe were maintained, deformation-induced phase transformation occurred during
deformation, as was expected in the present invention, whereby ductility and stiffness
were observed at a cryogenic temperature.
[0057] Furthermore, when at least one of C and N was subjected to solid solution as an interstitial
element in the metal matrix of the medium-entropy alloy of the present invention,
it was also confirmed that the strength of the alloy was increased due to the solid-solution
strengthening effect.
Deformation-induced phase transformation
[0058] FIG. 4 shows the analytical results of EBSD for phase transformation of the medium-entropy
alloy of Example 3 during deformation at room temperature and at a cryogenic temperature
according to the present invention.
[0059] As shown in FIG. 4, the alloy of Example 3 included a very small amount of the BCC
phase and was composed mainly of the metastable FCC phase before deformation, and
the fraction of the BCC phase was remarkably increased after deformation at room temperature
(298 K) and at a cryogenic temperature (77 K). In particular, phase transformation
from the FCC phase into the BCC phase occurs over the entire region after deformation
at a cryogenic temperature, and this phase transformation contributes greatly to the
improvement of cryogenic mechanical properties, as shown in FIG. 3.
[0060] Therefore, with regard to the cryogenic mechanical properties, the fraction of the
FCC phase before deformation is preferably set to 50% or more.
[Table 5]
|
Before deformation (vol%) |
After deformation (298 K) (vol%) |
After deformation (77 K) (vol%) |
Comparative Example 1 |
91.26 |
93.96 |
98.99 |
Example 1 |
0.34 |
15.07 |
28.46 |
Example 2 |
0.38 |
20.26 |
36.12 |
Example 3 |
0.41 |
27.68 |
56.71 |
Example 4 |
25.68 |
62.23 |
85.08 |
Comparative Example 2 |
87.81 |
89.20 |
94.87 |
[0061] Table 5 shows the results of ferritescope measurement of the BCC phase fraction (vol%)
of the alloys of Comparative Examples 1 and 2 and Examples 1 to 4 according to the
present invention, before deformation and after deformation at room temperature and
at a cryogenic temperature.
[0062] As is apparent from Table 5, the alloys of Examples 1 to 3 included a small amount
of the BCC phase before deformation and were increased in the fraction of the BCC
phase due to phase transformation between deformation at room temperature and deformation
at a cryogenic temperature. Also, the alloy of Example 4 was relatively increased
in BCC phase stability compared to the alloys of Examples 1 to 3, and thus it was
confirmed that 25.68 at% of the BCC phase was included before deformation and that
the fraction of the BCC phase was increased due to phase transformation between deformation
at room temperature and deformation at a cryogenic temperature. The alloys of Comparative
Examples 1 and 2 were very high in BCC phase stability compared to the alloys of Examples
1 to 4, and thus it was confirmed that 91.26 at% and 87.81 at% of the BCC phases,
respectively, were included before deformation and that the fraction of the BCC phase
was increased due to phase transformation between deformation at room temperature
and deformation at a cryogenic temperature.
1. A medium-entropy alloy, comprising 6 to 15 at% of Cr, 50 to 64 at% of Fe, 13 to 25
at% of Co, 13 to 25 at% of Ni, and a remainder of inevitable impurities, wherein deformation-induced
phase transformation from a face-centered cubic (FCC) phase into a body-centered cubic
(BCC) phase occurs upon plastic deformation.
2. The medium-entropy alloy of claim 1, wherein the deformation-induced phase transformation
occurs in a metastable FCC phase.
3. The medium-entropy alloy of claim 1, wherein an amount of the Cr is 7.5 to 12.5 at%.
4. The medium-entropy alloy of claim 3, wherein an amount of the Fe is 57.5% to 62.5
at%.
5. The medium-entropy alloy of claim 1, wherein the Co is substitutable with at least
one selected from among Mo and Al.
6. The medium-entropy alloy of claim 1 or 5, wherein the Ni is substitutable with Mn.
7. The medium-entropy alloy of claim 1 or 4, wherein at least one of C and N is included
in an amount of less than 1 at% based on a total at% of the medium-entropy alloy.
8. The medium-entropy alloy of claim 6, wherein at least one of C and N is included in
an amount of less than 1 at% based on a total at% of the medium-entropy alloy.
9. The medium-entropy alloy of claim 1, wherein the deformation occurs at a temperature
equal to or lower than room temperature (298 K).
10. The medium-entropy alloy of claim 2, wherein a fraction of the metastable FCC phase
is 50% or more.
11. The medium-entropy alloy of claim 1, wherein the medium-entropy alloy is composed
of a combination of a BCC phase and a metastable FCC phase, or is composed of a metastable
FCC phase alone.
12. The medium-entropy alloy of claim 1, wherein the medium-entropy alloy has a tensile
strength of 226 MPa or more and an elongation of 67% or more at room temperature (298
K).
13. The medium-entropy alloy of claim 1, wherein the medium-entropy alloy has a tensile
strength of 1024 MPa or more and an elongation of 47% or more at a cryogenic temperature
(77 K).