EP3660178A1 - Legierung mit mittelhoher entropie und hervorragenden kryogenen eigenschaften - Google Patents
Legierung mit mittelhoher entropie und hervorragenden kryogenen eigenschaften Download PDFInfo
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- EP3660178A1 EP3660178A1 EP17912348.4A EP17912348A EP3660178A1 EP 3660178 A1 EP3660178 A1 EP 3660178A1 EP 17912348 A EP17912348 A EP 17912348A EP 3660178 A1 EP3660178 A1 EP 3660178A1
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- entropy alloy
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/06—Ferrous alloys, e.g. steel alloys containing aluminium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/08—Ferrous alloys, e.g. steel alloys containing nickel
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/10—Ferrous alloys, e.g. steel alloys containing cobalt
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/10—Ferrous alloys, e.g. steel alloys containing cobalt
- C22C38/105—Ferrous alloys, e.g. steel alloys containing cobalt containing Co and Ni
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/22—Ferrous alloys, e.g. steel alloys containing chromium with molybdenum or tungsten
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/30—Ferrous alloys, e.g. steel alloys containing chromium with cobalt
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/38—Ferrous alloys, e.g. steel alloys containing chromium with more than 1.5% by weight of manganese
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/44—Ferrous alloys, e.g. steel alloys containing chromium with nickel with molybdenum or tungsten
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/52—Ferrous alloys, e.g. steel alloys containing chromium with nickel with cobalt
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/58—Ferrous alloys, e.g. steel alloys containing chromium with nickel with more than 1.5% by weight of manganese
Definitions
- 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.
- MEA medium-entropy alloy
- inexpensive Fe is included in an amount of 50 at% or more to thus exhibit high price competitiveness
- FCC face-centered cubic
- BCC body-centered cubic
- a high-entropy alloy 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.
- 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.
- 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.
- alloys are typically divided into high-entropy alloys, medium-entropy alloys (MEAs), and low-entropy alloys (LEAs), depending on the configurational entropy ( ⁇ S 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.
- Co 20 Cr 20 Fe 20 Mn 20 Ni 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.
- Patent Document U.S. Patent Application Publication No. 2002/0159914
- Non-Patent Document (Non-Patent Document) 1.
- 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.
- 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.
- 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.
- 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).
- 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.
- 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.
- 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.
- phase in a metastable state 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.
- 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.
- 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.
- 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%.
- 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%.
- 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%.
- 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%.
- the FCC phase is stabilized.
- the amount thereof preferably falls in the range of 13 to 25 at%.
- 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%.
- 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.
- the FCC phase is stabilized.
- the above element be added in an amount of less than 1 at%.
- 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.
- 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.
- 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.
- the fraction of the metastable FCC phase is not necessarily 50% or more.
- the medium-entropy alloy may have tensile strength of 500 MPa or more and elongation of 50% or more at room temperature (298 K).
- 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).
- Co, Cr, Fe, and Ni metals having purity of 99.9% or more were prepared.
- 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.
- 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.
- the cold-rolled alloy plate was annealed at 800°C for 10 min.
- 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.
- the cold-rolled alloy plate was annealed at 800°C for 10 min in the same manner as in Examples.
- 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.
- 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.
- 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.
- Comparative Example 1 was composed of the BCC phase
- Examples 1 to 4 were composed mainly of the metastable FCC phase
- Comparative Example 2 was composed mainly of the BCC phase and included a small amount of the FCC phase.
- 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.
- 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%.
- 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.
- 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.
- 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.
- 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).
- 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 .
- the fraction of the FCC phase before deformation is preferably set to 50% or more.
- 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.
- 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.
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Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| KR1020170094759A KR101910744B1 (ko) | 2017-07-26 | 2017-07-26 | 극저온 특성이 우수한 중엔트로피 합금 |
| PCT/KR2017/009364 WO2019022283A1 (ko) | 2017-07-26 | 2017-08-28 | 극저온 특성이 우수한 중엔트로피 합금 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| EP3660178A1 true EP3660178A1 (de) | 2020-06-03 |
| EP3660178A4 EP3660178A4 (de) | 2020-06-03 |
| EP3660178B1 EP3660178B1 (de) | 2022-10-19 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EP17912348.4A Active EP3660178B1 (de) | 2017-07-26 | 2017-08-28 | Legierung mit mittelhoher entropie und hervorragenden kryogenen eigenschaften |
Country Status (5)
| Country | Link |
|---|---|
| US (1) | US20210054486A1 (de) |
| EP (1) | EP3660178B1 (de) |
| JP (1) | JP2019532169A (de) |
| KR (1) | KR101910744B1 (de) |
| WO (1) | WO2019022283A1 (de) |
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| CN111705254A (zh) * | 2020-06-30 | 2020-09-25 | 江苏鑫信润科技股份有限公司 | 一种耐腐蚀动密封用CoNiFe中熵合金及其制备方法 |
| CN114231765A (zh) * | 2021-11-26 | 2022-03-25 | 北京北冶功能材料有限公司 | 一种高温合金棒材的制备方法与应用 |
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| USD1061623S1 (en) | 2022-08-03 | 2025-02-11 | Vulcan Industrial Holdings, LLC | Fluid end for a pumping system |
| CN115323240B (zh) * | 2022-08-29 | 2023-06-30 | 沈阳工业大学 | 一种高强韧亚稳态双相FeMnCrCo高熵合金及其制备方法 |
| CN115198162B (zh) * | 2022-09-19 | 2022-12-02 | 太原理工大学 | 高强韧异质多相“核壳”组织结构中熵合金及其制备方法 |
| CN115786795B (zh) * | 2022-11-24 | 2024-01-26 | 陕西科技大学 | 一种CrFe2Ni2NbxMy共晶中熵合金及其制备方法 |
| CN116145008B (zh) * | 2023-02-24 | 2025-03-28 | 南京理工大学 | 一种具有零场冷交换偏置效应的Mn2-xFeCoNi中熵合金材料及其制备方法 |
| CN116716585A (zh) * | 2023-05-22 | 2023-09-08 | 南方科技大学 | 一种耐摩擦合金薄膜及其制备方法与应用 |
| US12292121B2 (en) | 2023-08-10 | 2025-05-06 | Vulcan Industrial Holdings, LLC | Valve member including cavity, and related assemblies, systems, and methods |
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| US3673010A (en) * | 1970-05-19 | 1972-06-27 | Tohoku Special Steel Works Ltd | Cold-workable permanent magnet alloy |
| JPS5480570A (en) * | 1977-12-09 | 1979-06-27 | Tohoku Metal Ind Ltd | Metallic magnetic material for thermoo sensitive element and lead switch employing same |
| DE68919672T2 (de) * | 1988-07-08 | 1995-04-06 | Famcy Steel Corp | Anwendung von einer zweiphasigen eisen-mangan-aluminium-kohlenstofflegierung mit hoher dämpfungsfähigkeit. |
| JP3216824B2 (ja) * | 1991-10-25 | 2001-10-09 | 日立金属株式会社 | 高強度低熱膨張合金 |
| US20020159914A1 (en) | 2000-11-07 | 2002-10-31 | Jien-Wei Yeh | High-entropy multielement alloys |
| JP5059035B2 (ja) | 2009-01-30 | 2012-10-24 | 公益財団法人電磁材料研究所 | 高弾性・恒弾性合金及びその製造法並びに精密機器 |
| JP5486050B2 (ja) * | 2012-07-11 | 2014-05-07 | 公益財団法人電磁材料研究所 | 高弾性・恒弾性合金及びその製造法並びに精密機器 |
| JP6388381B2 (ja) * | 2014-07-23 | 2018-09-12 | 日立金属株式会社 | 合金構造体 |
| JP6536927B2 (ja) * | 2014-07-25 | 2019-07-03 | 日立金属株式会社 | 合金構造体 |
| KR101728936B1 (ko) * | 2014-07-28 | 2017-04-21 | 세종대학교산학협력단 | 우수한 강도 및 연성을 갖는 하이엔트로피 합금 |
| KR101708763B1 (ko) * | 2015-05-04 | 2017-03-08 | 한국과학기술연구원 | 고온 중성자 조사 손상에 강한 엔트로피 제어 bcc 합금 |
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2017
- 2017-07-26 KR KR1020170094759A patent/KR101910744B1/ko active Active
- 2017-08-28 US US16/308,517 patent/US20210054486A1/en not_active Abandoned
- 2017-08-28 JP JP2018565038A patent/JP2019532169A/ja active Pending
- 2017-08-28 EP EP17912348.4A patent/EP3660178B1/de active Active
- 2017-08-28 WO PCT/KR2017/009364 patent/WO2019022283A1/ko not_active Ceased
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN110157970A (zh) * | 2019-06-11 | 2019-08-23 | 沈阳航空航天大学 | 一种高强塑积CoCrNi中熵合金及其制备方法 |
| CN110157970B (zh) * | 2019-06-11 | 2021-01-05 | 沈阳航空航天大学 | 一种高强塑积CoCrNi中熵合金及其制备方法 |
| CN111705254A (zh) * | 2020-06-30 | 2020-09-25 | 江苏鑫信润科技股份有限公司 | 一种耐腐蚀动密封用CoNiFe中熵合金及其制备方法 |
| CN114231765A (zh) * | 2021-11-26 | 2022-03-25 | 北京北冶功能材料有限公司 | 一种高温合金棒材的制备方法与应用 |
| CN115074595A (zh) * | 2022-06-06 | 2022-09-20 | 北京科技大学 | 一种耐酸腐蚀非等原子比CoCrNi中熵合金及其制备方法 |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2019532169A (ja) | 2019-11-07 |
| WO2019022283A1 (ko) | 2019-01-31 |
| EP3660178B1 (de) | 2022-10-19 |
| EP3660178A4 (de) | 2020-06-03 |
| KR101910744B1 (ko) | 2018-10-22 |
| US20210054486A1 (en) | 2021-02-25 |
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