[go: up one dir, main page]

EP0643145A1 - High strength magnesium-based alloy materials and method for producing the same - Google Patents

High strength magnesium-based alloy materials and method for producing the same Download PDF

Info

Publication number
EP0643145A1
EP0643145A1 EP94111190A EP94111190A EP0643145A1 EP 0643145 A1 EP0643145 A1 EP 0643145A1 EP 94111190 A EP94111190 A EP 94111190A EP 94111190 A EP94111190 A EP 94111190A EP 0643145 A1 EP0643145 A1 EP 0643145A1
Authority
EP
European Patent Office
Prior art keywords
matrix
high strength
based alloy
alloy material
general formula
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Granted
Application number
EP94111190A
Other languages
German (de)
French (fr)
Other versions
EP0643145B1 (en
Inventor
Toshisuke Shibata
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
YKK Corp
Original Assignee
YKK Corp
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by YKK Corp filed Critical YKK Corp
Publication of EP0643145A1 publication Critical patent/EP0643145A1/en
Application granted granted Critical
Publication of EP0643145B1 publication Critical patent/EP0643145B1/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C23/00Alloys based on magnesium
    • C22C23/06Alloys based on magnesium with a rare earth metal as the next major constituent
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C23/00Alloys based on magnesium
    • C22C23/04Alloys based on magnesium with zinc or cadmium as the next major constituent

Definitions

  • the present invention relates to high strength magnesium-based alloy materials having superior mechanical properties and a method for producing the same.
  • Mg-Al, Mg-Al-Zn, Mg-Th-Zr, Mg-Th-Zn-Zr, Mg-Zn-Zr, Mg-Zn-Zr-RE rare earth element
  • these known alloys have been extensively used as light-weight structural component materials in a wide variety of applications, according to their properties.
  • rapidly solidified materials there are known alloys disclosed in Japanese Patent Laid-open No. 3-47,941.
  • magnesium-based alloy materials which have an advantageous combination of properties of high hardness, strength and thermal resistance and which are useful as lightweight and high strength materials (i.e., high specific strength materials) and have a superior ductility.
  • a high strength magnesium-based alloy material having a microcrystalline composite structure, the alloy material consisting of a composition represented by the general formula (I): Mg a Nd b Zn c , wherein a, b and c are, in atomic %, 80 ⁇ a ⁇ 99, 1 ⁇ b ⁇ 12 and 0 ⁇ c ⁇ 12.
  • the present invention also provides a high strength magnesium-based alloy material having a microcrystalline composite structure, the alloy material consisting of a composition represented by the general formula (II): Mg a' Nd b' Zn c' , wherein a', b' and c' are, in atomic %, 95 ⁇ a' ⁇ 99, 1 ⁇ b' ⁇ 3 and 0 ⁇ c' ⁇ 3.
  • a', b' and c' are, in atomic %, 95 ⁇ a' ⁇ 99, 1 ⁇ b' ⁇ 3 and 0 ⁇ c' ⁇ 3.
  • the aforesaid high strength magnesium-based alloy materials are produced by a method comprising: rapidly solidifying a molten alloy so as to form a fine-grained matrix phase, the molten alloy consisting of the composition represented by the above-defined general formula (I) or (II); and subjecting the resultant rapidly solidified alloy to plastic working at a prescribed heating temperature for work hardening, thereby forming a microcrystalline composite structure having a uniform dispersion of very fine intermetallic compounds in the matrix.
  • the matrix in the composite structure consists of an Mg matrix having a hexagonal close-packed (hcp) structure and intermetallic compounds consisting of a non-equilibrium phase having a face-centered cubic (hcp) structure and/or other intermetallic compound phases, such as an Mg12Nd phase, are finely and uniformly dispersed throughout the matrix .
  • the present invention provides the above-defined high strength magnesium-based alloy materials consisting of a composition represented by the general formula (I) or (II).
  • the ranges of a, b and c are so limited that the above-defined alloy can be obtained with the aforesaid microcrystalline composite structure by industrial rapid cooling techniques, such as liquid quenching.
  • fine hcp-Mg precipitates as a host matrix, and finer intermetallic compounds of a non-equilibrium fcc phase formed from, at least, Mg and Nd and/or Mg12Nd phase, etc. are uniformly and finely distributed throughout the hcp-Mg matrix.
  • the intermetallic compounds comprising the non-equilibrium fcc phase which is formed from, at least, Mg and Nd and which has a good compatibility with the matrix of hcp-Mg, are uniformly and finely dispersed in the matrix, the Mg matrix is strengthened and the strength of the alloy is outstandingly improved.
  • Nd makes it possible to form the above-mentioned composite structure having a dispersion of intermetallic compounds consisting of a non-equilibrium fcc phase, which is formed from, at least, Nd and Mg, and/or other intermetallic compounds, such as an Mg12Nd phase, while suppressing the grain growth of the matrix phase. Since the intermetallic compounds can be formed in large quantities in the presence of a small amount of Nd, it is possible to obtain alloys having a high strength on an Mg-rich side so that high specific-strength materials can be obtained.
  • Another alloying element Zn transforms the non-equilibrium phase to a more stable non-equilibrium phase of fcc structure so that the intermetallic compounds having a good compatibility with the magnesium matrix ( ⁇ phase) uniformly and finely disperse in the matrix.
  • the hardness and strength of the resultant alloys are improved and a high thermal resistance is imparted to the alloys by suppressing coarsening of the microcrystalline structure of the alloys at high temperatures.
  • a molten alloy having the above-defined composition is rapidly solidified so as to obtain a fine-grained matrix phase.
  • a cooling rate of 102-106 K/sec is particularly effective.
  • the resultant rapidly solidified alloy is heated to a prescribed temperature and subjected to plastic working.
  • magnesium alloy materials having a microcrystalline composite structure composed of an hcp Mg matrix and, homogeneously distributed in the matrix, intermetallic compounds consisting of a non-equilibrium fcc phase and/or other intermetallic compound phases, such as an Mg12Nd phase formed of Mg and Nd.
  • the non-equilibrium fcc phase may be formed either during rapid solidification or during plastic working.
  • the plastic working is preferably performed at a temperature of 50 to 500°C.
  • a temperature lower than 50°C cannot provide a sound material due to an excessive deformation resistance.
  • a temperature exceeding 500°C causes a considerable grain growth, thereby lowering the strength.
  • the magnesium matrix and the intermetallic compounds formed by the above production method have a grain size ranging from 200 nm to 600 nm and a particle size ranging from 10 nm to 400 nm, respectively.
  • the alloys may have superior properties as superplastic working materials.
  • a molten alloy having a given composition was prepared using a high-frequency melting furnace.
  • the molten alloy was subjected to a single-roller melt-spinning technique, which is one of the rapid solidification techniques, at a cooling of 102-106 K/sec and a rapidly solidified material comprising a fine-grained matrix phase.
  • the thus obtained rapidly solidified material was subjected to hot-extrusion at a temperature of 320°C under an applied pressure of 1240-1628 MPa, while suppressing the grain growth of the matrix phase.
  • the thus obtained extruded material had a microcrystalline composite structure having a dispersion of fine intermetallic compounds.
  • test samples having the compositions (by atomic %) given in Table 1 were produced.
  • Comparative extruded materials having compositions falling outside the compositional range of the present invention were produced under the same processing conditions as described above.
  • the comparative materials are disclosed in Japanese Patent Application Laid-Open No. 3-47,941 hereinbefore described.
  • test sample was subjected to X-ray diffraction and measured for its mechanical properties, i.e., tensile strength ( ⁇ B ), plastic elongation ( ⁇ f ), Young's modulus (E), specific strength ( ⁇ B / ⁇ ). The results are shown on the right-hand column of Table 1. The specific strength was obtained by dividing tensile strength by density for each sample. Further, the test samples were observed by a transmission electron microscope (TEM).
  • TEM transmission electron microscope
  • Mg97Nd3 comprised an hcp-Mg matrix having a grain size of 200 nm to 600 nm and, homogeneously distributed in the matrix, an intermetallic compound of Mg12Nd formed of Mg and Nd and having a particle size of 250 nm to 400 nm.
  • Mg96Nd3Zn1 was composed of an hcp-Mg matrix having a grain size of 200 nm to 300 nm and, homogeneously distributed in the matrix, non-equilibrium fcc phase intermetallic compounds formed of Mg and Nd and/or Zn with a particle size of 10 nm to 200 nm.
  • every test sample of the present invention exhibited superior mechanical properties, i.e., a tensile strength of not less than 500 MPa, a plastic elongation of not less than 0.4%, a Young's modulus of at least 37 GPa and a specific strength of not less than 280 MPa.
  • the magnesium-based alloys of the present invention are superior in plastic elongation over the comparative test samples, they can be successfully subjected to various working operations and exhibit a sufficient durability to permit a high degree of working (plastic working).
  • the Mg content exceeded 95 atomic % in the Mg-Nd-Zn alloys, the plastic elongation surprisingly increased, although any significant change was hardly detected in the tensile strength, Young's modulus and specific strength.
  • the magnesium-based alloys of the present invention have high levels of strength and heat-resistance, they are very useful as high strength materials and high heat-resistant materials.
  • the magnesium-based alloys are also useful as high specific-strength materials because of their high specific strength. Still further, since the alloys exhibit superior elongation at room temperature and Young's module at room temperature, they can be successfully subjected to various working operations and exhibit a sufficient durability to permit a high degree of working (plastic working).

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
  • Organic Chemistry (AREA)
  • Powder Metallurgy (AREA)

Abstract

High strength magnesium-based alloy materials having a microcrystalline composite structure, the alloy materials consisting of a composition represented by the general formula (I): MgaNdbZnc, wherein a, b and c are, in atomic %, 80 ≦ a ≦ 99, 1 ≦ b ≦ 12 and 0 ≦ c ≦ 12; or the general formula (II): Mga'Ndb'Znc', wherein a', b' and c' are, in atomic %, 95 < a' ≦ 99, 1 ≦ b' ≦ 3 and 0 ≦ c' ≦ 3. The alloy materials have superior mechanical properties as high specific strength materials and plastic working materials and are produced by rapidly solidifying a molten alloy represented by the general formula (I) or (II) so as to form a fine-grained matrix phase; and subjecting the resultant rapidly solidified alloy to plastic working at a prescribed heating temperature for work hardening, thereby forming a microcrystalline composite structure having a dispersion of the fine intermetallic compounds in the matrix.

Description

    BACKGROUND OF THE INVENTION 1. Field of the Invention
  • The present invention relates to high strength magnesium-based alloy materials having superior mechanical properties and a method for producing the same.
  • 2. Description of the Prior Art
  • As conventional magnesium-based alloys, there are known Mg-Al, Mg-Al-Zn, Mg-Th-Zr, Mg-Th-Zn-Zr, Mg-Zn-Zr, Mg-Zn-Zr-RE (RE: rare earth element), etc. and these known alloys have been extensively used as light-weight structural component materials in a wide variety of applications, according to their properties. Further, as rapidly solidified materials, there are known alloys disclosed in Japanese Patent Laid-open No. 3-47,941.
  • However, under the present circumstances, known various types of magnesium-based alloys, as set forth above, have a low hardness and strength. Although the alloys disclosed in Japanese Patent Laid-open No. 3-47,941 have superior hardness and tensile strength, they still leave some room for further improvement in thermal stability and ductility. Further, in the Japanese Patent specification, there is no specific mention about Mg-Nd-Zn alloys, which are contemplated by the present invention, and most of the alloys disclosed therein are alloys including Mg in an amount of 70-80 atomic %.
  • SUMMARY OF THE INVENTION
  • In view of the foregoing, it is an object of the present invention to provide magnesium-based alloy materials which have an advantageous combination of properties of high hardness, strength and thermal resistance and which are useful as lightweight and high strength materials (i.e., high specific strength materials) and have a superior ductility.
  • According to the present invention, there is provided a high strength magnesium-based alloy material having a microcrystalline composite structure, the alloy material consisting of a composition represented by the general formula (I): MgaNdbZnc, wherein a, b and c are, in atomic %, 80 ≦ a ≦ 99, 1 ≦ b ≦ 12 and 0 ≦ c ≦ 12.
  • The present invention also provides a high strength magnesium-based alloy material having a microcrystalline composite structure, the alloy material consisting of a composition represented by the general formula (II): Mga'Ndb'Znc', wherein a', b' and c' are, in atomic %, 95 < a' ≦ 99, 1 ≦ b' ≦ 3 and 0 ≦ c' ≦ 3.
  • The aforesaid high strength magnesium-based alloy materials are produced by a method comprising:
       rapidly solidifying a molten alloy so as to form a fine-grained matrix phase, the molten alloy consisting of the composition represented by the above-defined general formula (I) or (II); and
       subjecting the resultant rapidly solidified alloy to plastic working at a prescribed heating temperature for work hardening, thereby forming a microcrystalline composite structure having a uniform dispersion of very fine intermetallic compounds in the matrix.
  • The matrix in the composite structure consists of an Mg matrix having a hexagonal close-packed (hcp) structure and intermetallic compounds consisting of a non-equilibrium phase having a face-centered cubic (hcp) structure and/or other intermetallic compound phases, such as an Mg₁₂Nd phase, are finely and uniformly dispersed throughout the matrix .
  • DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
  • As described above, the present invention provides the above-defined high strength magnesium-based alloy materials consisting of a composition represented by the general formula (I) or (II). In the above-defined general formula (I), the ranges of a, b and c are so limited that the above-defined alloy can be obtained with the aforesaid microcrystalline composite structure by industrial rapid cooling techniques, such as liquid quenching.
  • The reason why the ranges of a', b' and c' of the general formula (II) are limited as defined above is that since a large amount of intermetallic compounds are formed with a small amount of Nd, the rapidly solidified material obtained from the alloy composition has a high strength on a higher Mg content side as compared with the rapidly solidified material represented by the general formula (I) and is useful as a high specific strength material. Further, the addition of solute elements can be saved.
  • As a further important reason, in the above-defined compositional ranges, fine hcp-Mg precipitates as a host matrix, and finer intermetallic compounds of a non-equilibrium fcc phase formed from, at least, Mg and Nd and/or Mg₁₂Nd phase, etc. are uniformly and finely distributed throughout the hcp-Mg matrix. Especially, when the intermetallic compounds comprising the non-equilibrium fcc phase, which is formed from, at least, Mg and Nd and which has a good compatibility with the matrix of hcp-Mg, are uniformly and finely dispersed in the matrix, the Mg matrix is strengthened and the strength of the alloy is outstandingly improved. However, when the Mg content is 95 atomic % or less, a very high ductility as obtained in the case of Mg contents exceeding 95 atomic % cannot be expected because the proportion of the intermetallic compounds dispersed in the matrix becomes excessive with respect to the entire alloy.
  • In the magnesium-based alloys of the present invention, Nd makes it possible to form the above-mentioned composite structure having a dispersion of intermetallic compounds consisting of a non-equilibrium fcc phase, which is formed from, at least, Nd and Mg, and/or other intermetallic compounds, such as an Mg₁₂Nd phase, while suppressing the grain growth of the matrix phase. Since the intermetallic compounds can be formed in large quantities in the presence of a small amount of Nd, it is possible to obtain alloys having a high strength on an Mg-rich side so that high specific-strength materials can be obtained.
  • Another alloying element Zn transforms the non-equilibrium phase to a more stable non-equilibrium phase of fcc structure so that the intermetallic compounds having a good compatibility with the magnesium matrix (α phase) uniformly and finely disperse in the matrix. As a result, the hardness and strength of the resultant alloys are improved and a high thermal resistance is imparted to the alloys by suppressing coarsening of the microcrystalline structure of the alloys at high temperatures.
  • In the production of the high strength magnesium-based alloy materials of the present invention, a molten alloy having the above-defined composition is rapidly solidified so as to obtain a fine-grained matrix phase. In the rapidly solidification step, a cooling rate of 10²-10⁶ K/sec is particularly effective. The resultant rapidly solidified alloy is heated to a prescribed temperature and subjected to plastic working. As a result, it is possible to obtain magnesium alloy materials having a microcrystalline composite structure composed of an hcp Mg matrix and, homogeneously distributed in the matrix, intermetallic compounds consisting of a non-equilibrium fcc phase and/or other intermetallic compound phases, such as an Mg₁₂Nd phase formed of Mg and Nd. The non-equilibrium fcc phase may be formed either during rapid solidification or during plastic working. The plastic working is preferably performed at a temperature of 50 to 500°C. A temperature lower than 50°C cannot provide a sound material due to an excessive deformation resistance. On the other hand, a temperature exceeding 500°C causes a considerable grain growth, thereby lowering the strength.
  • The magnesium matrix and the intermetallic compounds formed by the above production method have a grain size ranging from 200 nm to 600 nm and a particle size ranging from 10 nm to 400 nm, respectively.
  • Further, by controlling the matrix grain size and the intermetallic compound particle size of the inventive alloys to the above-defined ranges, the alloys may have superior properties as superplastic working materials.
  • The present invention will be illustrated in more detail by the following examples.
  • Examples
  • A molten alloy having a given composition was prepared using a high-frequency melting furnace. The molten alloy was subjected to a single-roller melt-spinning technique, which is one of the rapid solidification techniques, at a cooling of 10²-10⁶ K/sec and a rapidly solidified material comprising a fine-grained matrix phase.
  • The thus obtained rapidly solidified material was subjected to hot-extrusion at a temperature of 320°C under an applied pressure of 1240-1628 MPa, while suppressing the grain growth of the matrix phase. The thus obtained extruded material had a microcrystalline composite structure having a dispersion of fine intermetallic compounds.
  • According to the processing conditions as set forth above, test samples (extruded materials) having the compositions (by atomic %) given in Table 1 were produced. Comparative extruded materials having compositions falling outside the compositional range of the present invention were produced under the same processing conditions as described above. The comparative materials are disclosed in Japanese Patent Application Laid-Open No. 3-47,941 hereinbefore described.
  • Each test sample was subjected to X-ray diffraction and measured for its mechanical properties, i.e., tensile strength (σB), plastic elongation (εf), Young's modulus (E), specific strength (σB/ρ). The results are shown on the right-hand column of Table 1. The specific strength was obtained by dividing tensile strength by density for each sample. Further, the test samples were observed by a transmission electron microscope (TEM). The results of the TEM observation were as follows:
       Mg₉₇Nd₃ comprised an hcp-Mg matrix having a grain size of 200 nm to 600 nm and, homogeneously distributed in the matrix, an intermetallic compound of Mg₁₂Nd formed of Mg and Nd and having a particle size of 250 nm to 400 nm.
  • Mg₉₆Nd₃Zn₁ was composed of an hcp-Mg matrix having a grain size of 200 nm to 300 nm and, homogeneously distributed in the matrix, non-equilibrium fcc phase intermetallic compounds formed of Mg and Nd and/or Zn with a particle size of 10 nm to 200 nm. Table 1
    No. Mg Nd Zn Phase σB (MPa) Ef (%) E (MPa) σB/ρ
    1 97 3 - Mg+unknown +Mg₁₂Nd 562 0.44 38 285
    2 96 3 1 Mg+non-equilibrium fcc 617 3.7 37 307
    3 95.5 2.5 2 Mg+non-equilibrium fcc 611 4.7 39 306
    4 95 3 2 Mg+non-equilibrium fcc 633 1.0 39 310
    Comparative Test Sample
    1 Mg 90 Cu 5 La 5 Mg+Mg₂Cu +Mg₉La 872 0.1 47 382
    2 Mg 80 Cu 10 Y 10 Mg+Mg₂Cu +Mg₂₄Y₅ 901 0.05 52 360
  • As is evident from Table 1, every test sample of the present invention exhibited superior mechanical properties, i.e., a tensile strength of not less than 500 MPa, a plastic elongation of not less than 0.4%, a Young's modulus of at least 37 GPa and a specific strength of not less than 280 MPa. Particularly, since the magnesium-based alloys of the present invention are superior in plastic elongation over the comparative test samples, they can be successfully subjected to various working operations and exhibit a sufficient durability to permit a high degree of working (plastic working). When the Mg content exceeded 95 atomic % in the Mg-Nd-Zn alloys, the plastic elongation surprisingly increased, although any significant change was hardly detected in the tensile strength, Young's modulus and specific strength.
  • Since the magnesium-based alloys of the present invention have high levels of strength and heat-resistance, they are very useful as high strength materials and high heat-resistant materials. The magnesium-based alloys are also useful as high specific-strength materials because of their high specific strength. Still further, since the alloys exhibit superior elongation at room temperature and Young's module at room temperature, they can be successfully subjected to various working operations and exhibit a sufficient durability to permit a high degree of working (plastic working).

Claims (7)

  1. A high strength magnesium-based alloy material having a microcrystalline composite structure, the alloy material consisting of a composition represented by the general formula (I): MgaNdbZnc, wherein a, b and c are, in atomic %, 80 ≦ a ≦ 99, 1 ≦ b ≦ 12 and 0 ≦ c ≦ 12.
  2. A high strength magnesium-based alloy material having a microcrystalline composite structure, the alloy material consisting of a composition represented by the general formula (II): Mga'Ndb'Znc', wherein a', b' and c' are, in atomic %, 95 < a' ≦ 99, 1 ≦ b' ≦ 3 and 0 ≦ c' ≦ 3.
  3. A high strength magnesium-based alloy material as claimed in Claim 1 or 2, wherein the magnesium-based alloy material has a microcrystalline composite structure consisting of an Mg matrix having a hexagonal close-packed structure, and, homogeneously and finely distributed in the matrix, intermetallic compounds consisting of a non-equilibrium phase having a face-centered cubic structure and/or an Mg₁₂Nd phase.
  4. A high strength magnesium-based alloy material as claimed in Claim 3, wherein the intermetallic compounds contain at least an intermetallic compound consisting of a non-equilibrium phase having a face-centered cubic structure.
  5. A method for producing a high strength magnesium-based alloy material, comprising:
       rapidly solidifying a molten alloy so as to form a fine-grained matrix phase, the molten alloy consisting of a composition represented by the general formula (I): MgaNdbZnc, wherein a, b and c are, in atomic %, 80 ≦ a ≦ 99, 1 ≦ b ≦ 12 and 0 ≦ c ≦ 12; and
       subjecting the resultant rapidly solidified alloy to plastic working at a prescribed heating temperature for work hardening, thereby forming a microcrystalline composite structure having a dispersion of fine intermetallic compounds in the matrix.
  6. A method for producing a high strength magnesium-based alloy material, comprising:
       rapidly solidifying a molten alloy so as to form a fine-grained matrix phase, the molten alloy consisting of a composition represented by the general formula (II): Mga'Ndb'Znc', wherein a', b' and c' are, in atomic %, 95 < a' ≦ 99, 1 ≦ b' ≦ 3 and 0 ≦ c' ≦ 3; and
       subjecting the resultant rapidly solidified alloy to plastic working at a prescribed heating temperature for work hardening, thereby forming a microcrystalline composite structure having a dispersion of fine intermetallic compounds in the matrix.
  7. A method as claimed in Claim 5 or 6, wherein the prescribed heating temperature ranges from 50 to 500°C.
EP19940111190 1993-08-04 1994-07-18 High strength magnesium-based alloy materials and method for producing the same Expired - Lifetime EP0643145B1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP5193483A JP2807400B2 (en) 1993-08-04 1993-08-04 High strength magnesium-based alloy material and method of manufacturing the same
JP193483/93 1993-08-04

Publications (2)

Publication Number Publication Date
EP0643145A1 true EP0643145A1 (en) 1995-03-15
EP0643145B1 EP0643145B1 (en) 1998-12-23

Family

ID=16308787

Family Applications (1)

Application Number Title Priority Date Filing Date
EP19940111190 Expired - Lifetime EP0643145B1 (en) 1993-08-04 1994-07-18 High strength magnesium-based alloy materials and method for producing the same

Country Status (3)

Country Link
EP (1) EP0643145B1 (en)
JP (1) JP2807400B2 (en)
DE (1) DE69415447T2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000060131A2 (en) * 1999-04-03 2000-10-12 Volkswagen Aktiengesellschaft Highly ductile magnesium alloys, method of preparing same and their use

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5429702B2 (en) * 2006-08-03 2014-02-26 独立行政法人物質・材料研究機構 Magnesium alloy and manufacturing method thereof
JP5721043B2 (en) * 2010-10-20 2015-05-20 住友電気工業株式会社 Magnesium alloy and damping material

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989011552A1 (en) * 1988-05-23 1989-11-30 Allied-Signal Inc. Superplastic forming of rapidly solidified magnesium base metal alloys
WO1991013181A1 (en) * 1990-02-20 1991-09-05 Allied-Signal Inc. Method for superplastic forming of rapidly solidified magnesium base metal alloys
EP0531165A1 (en) * 1991-09-06 1993-03-10 Tsuyoshi Masumoto High-strength amorphous magnesium alloy and method for producing the same

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4765954A (en) * 1985-09-30 1988-08-23 Allied Corporation Rapidly solidified high strength, corrosion resistant magnesium base metal alloys
JP2511526B2 (en) * 1989-07-13 1996-06-26 ワイケイケイ株式会社 High strength magnesium base alloy
JP3238516B2 (en) * 1993-03-15 2001-12-17 健 増本 High strength magnesium alloy and method for producing the same

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1989011552A1 (en) * 1988-05-23 1989-11-30 Allied-Signal Inc. Superplastic forming of rapidly solidified magnesium base metal alloys
WO1991013181A1 (en) * 1990-02-20 1991-09-05 Allied-Signal Inc. Method for superplastic forming of rapidly solidified magnesium base metal alloys
EP0531165A1 (en) * 1991-09-06 1993-03-10 Tsuyoshi Masumoto High-strength amorphous magnesium alloy and method for producing the same

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000060131A2 (en) * 1999-04-03 2000-10-12 Volkswagen Aktiengesellschaft Highly ductile magnesium alloys, method of preparing same and their use
WO2000060131A3 (en) * 1999-04-03 2001-01-11 Volkswagen Ag Highly ductile magnesium alloys, method of preparing same and their use

Also Published As

Publication number Publication date
EP0643145B1 (en) 1998-12-23
DE69415447T2 (en) 1999-07-08
DE69415447D1 (en) 1999-02-04
JP2807400B2 (en) 1998-10-08
JPH0748647A (en) 1995-02-21

Similar Documents

Publication Publication Date Title
US4661172A (en) Low density aluminum alloys and method
EP0561375A2 (en) High-strength aluminum alloy
DE69502867T2 (en) High strength aluminum alloy
EP1640466B1 (en) Magnesium alloy and production process thereof
EP0534470B1 (en) Superplastic aluminum-based alloy material and production process thereof
EP1359232B2 (en) Method of improving fracture toughness in aluminium-lithium alloys
JPS63157831A (en) Heat-resisting aluminum alloy
EP0676480A1 (en) High strength Mg-Si type aluminum alloy
CA2135790C (en) Low density, high strength al-li alloy having high toughness at elevated temperatures
US4049426A (en) Copper-base alloys containing chromium, niobium and zirconium
EP0587186B1 (en) Aluminum-based alloy with high strength and heat resistance
EP0475101B1 (en) High strength aluminum-based alloys
US5647919A (en) High strength, rapidly solidified alloy
EP0796925A1 (en) High-strength and high-ductility aluminum-base alloy
US4525325A (en) Copper-nickel-tin-cobalt spinodal alloy
US4693747A (en) Alloy having improved fatigue crack growth resistance
JPH0794698B2 (en) High strength aluminum alloy with excellent resistance to stress corrosion cracking
EP0643145B1 (en) High strength magnesium-based alloy materials and method for producing the same
Marshall et al. Effect of consolidation route on structure and property control in rapidly solidified Al–Cr–Zr–Mn povvder alloy for high temperature service
EP0661384B1 (en) Heat resistant magnesium alloy
EP0577944B1 (en) High-strength aluminum-based alloy, and compacted and consolidated material thereof
EP0534155B1 (en) Compacted and consolidated aluminum-based alloy material and production process thereof
US5277717A (en) Rapidly solidified aluminum lithium alloys having zirconium for aircraft landing wheel applications
EP0524527B1 (en) Compacted and consolidated aluminium-based alloy material and production process thereof
CA2079327A1 (en) Double aged rapidly solidified aluminum-lithium alloys

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

AK Designated contracting states

Kind code of ref document: A1

Designated state(s): DE FR GB

17P Request for examination filed

Effective date: 19950206

17Q First examination report despatched

Effective date: 19971121

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAG Despatch of communication of intention to grant

Free format text: ORIGINAL CODE: EPIDOS AGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAH Despatch of communication of intention to grant a patent

Free format text: ORIGINAL CODE: EPIDOS IGRA

GRAA (expected) grant

Free format text: ORIGINAL CODE: 0009210

AK Designated contracting states

Kind code of ref document: B1

Designated state(s): DE FR GB

ET Fr: translation filed
REF Corresponds to:

Ref document number: 69415447

Country of ref document: DE

Date of ref document: 19990204

PLBE No opposition filed within time limit

Free format text: ORIGINAL CODE: 0009261

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT

26N No opposition filed
PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: GB

Payment date: 20000713

Year of fee payment: 7

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: DE

Payment date: 20000831

Year of fee payment: 7

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: GB

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20010718

GBPC Gb: european patent ceased through non-payment of renewal fee

Effective date: 20010718

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: FR

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020329

PG25 Lapsed in a contracting state [announced via postgrant information from national office to epo]

Ref country code: DE

Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES

Effective date: 20020501

REG Reference to a national code

Ref country code: FR

Ref legal event code: ST

PGFP Annual fee paid to national office [announced via postgrant information from national office to epo]

Ref country code: FR

Payment date: 20020709

Year of fee payment: 9