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EP0072893A1 - Alliages vitreux présentant une combinaison de perméabilité élevée, faible champ coercitif, faible perte dans le fer en alternatif, force d'excitation réduite et grande stabilité thermique - Google Patents

Alliages vitreux présentant une combinaison de perméabilité élevée, faible champ coercitif, faible perte dans le fer en alternatif, force d'excitation réduite et grande stabilité thermique Download PDF

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Publication number
EP0072893A1
EP0072893A1 EP82104504A EP82104504A EP0072893A1 EP 0072893 A1 EP0072893 A1 EP 0072893A1 EP 82104504 A EP82104504 A EP 82104504A EP 82104504 A EP82104504 A EP 82104504A EP 0072893 A1 EP0072893 A1 EP 0072893A1
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EP
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Prior art keywords
atom percent
low
boron
iron
particles
Prior art date
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Granted
Application number
EP82104504A
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German (de)
English (en)
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EP0072893B1 (fr
Inventor
Ryusuke Hasegawa
Gordon Edward Fish
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Allied Corp
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Allied Corp
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Classifications

    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C27/00Alloys based on rhenium or a refractory metal not mentioned in groups C22C14/00 or C22C16/00
    • C22C27/02Alloys based on vanadium, niobium, or tantalum
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C45/00Amorphous alloys
    • C22C45/02Amorphous alloys with iron as the major constituent

Definitions

  • the invention relates to metallic glasses having high permeability, low magnetostriction, low coercivity, low ac core loss, low exciting power and high thermal stability.
  • metallic glasses are metastable materials lacking any long range order.
  • X-ray diffraction scans of glassy metal alloys show only a diffuse halo similar to that observed for inorganic oxide glasses.
  • Metallic glasses have been disclosed in U.S. Patent 3,856,513, issued December 24, 1974 to H.S. Chen et al. These alloys include compositions having the formula M a Y b Z c , where M is a metal selected from the group consisting of iron, nickel, cobalt, vanadium and chromium, Y is an element selected from the group consisting of phosphorus, boron and carbon and Z is an element selected from the group consisting of aluminum, silicon, tin, germanium, indium, antimony and beryllium, "a” ranges from about 60 to 90 atom percent, "b” ranges from about 10 to 30 atom percent and "c” ranges from about 0.1 to 15 atom percent.
  • M is a metal selected from the group consisting of iron, nickel, cobalt, vanadium and chromium
  • Y is an element selected from the group consisting of phosphorus, boron and carbon
  • Z is an element selected from the group consisting of aluminum, silicon, tin,
  • metallic glassy wires having the formula T i X j' where T is at least one transition metal and X is an element selected from the group consisting of phosphorus, boron, carbon, aluminum, silicon, tin, germanium, indium, beryllium and antimony, "i” ranges from about 70 to 87 atom percent and "j” ranges from about 13 to 30 atom percent.
  • T is at least one transition metal
  • X is an element selected from the group consisting of phosphorus, boron, carbon, aluminum, silicon, tin, germanium, indium, beryllium and antimony
  • i ranges from about 70 to 87 atom percent
  • j ranges from about 13 to 30 atom percent.
  • Metallic glasses are also disclosed in U.S. Patent No. 4,067,732 issued January 10, 1978. These glassy alloys include compositions having the formula M a M' b Cr c M" d B e , where M is one iron group element (iron, cobalt and nickel), M' is at least one of the two remaining iron group elements, M" is at least one element of vanadium, manganese, molybdenum, tungsten, niobium and tantalum, B is boron, "a” ranges from about 40 to 85 atom percent, “b” ranges from 0 to about 45 atom percent, "c” and “d” both range from 0 to about 20 atom percent and “e” ranges from about 15 to 25 atom percent, with the provision that "b", "c” and “d” cannot be zero simultaneously.
  • Such glassy alloys are disclosed as having an unexpected combination of improved ultimate tensile strength, improved hardness and improved thermal stability.
  • metallic glasses possessing a combination of higher permeability, lower magnetostriction, lower coercivity, lower core loss, lower exciting power and higher thermal stability than prior art metallic glasses are required for specific applications such as tape recorder head, relay cores, transformers and the like.
  • metallic glasses having a combination of high permeability, low magnetostriction, low coercivity, low ac core loss, low exciting power and high thermal stability.
  • the metallic glasses consist essentially of about 66 to 82 atom percent of iron, from 1 to about 8 atom percent of which metal may be replaced with at least one of nickel and cobalt, about 1 to about 6 atom percent of at least one element selected from the group consisting of chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and hafnium, about 17 to 28 atom percent of boron, from 0.5 to about 6 atom percent of boron being, optionally, replaced with silicon and up to about 2 atom percent of boron being, optionally, replaced with carbon, plus incidental impurities.
  • the metallic glasses of the invention are suitable for use in tape recorder heads, relay cores, transformers and the like.
  • the metallic glasses of the invention are characterized by a combination of high permeability, low saturation magnetostriction, low coercivity, low ac core loss, low exciting power and high thermal stability.
  • the glassy alloys of the invention consist essentially of about 66 to 82 atom percent iron, from 1 to about 8 atom percent of which metal may be replaced with at least one of nickel and cobalt, about 1 to 6 atom percent of at least one element selected from the group consisting of chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and hafnium, about 17 to 28 atom percent of boron, from 0.5 to about 6 atom percent of which metalloid may be replaced with silicon and up to 2 atom percent of which metalloid may be replaced with carbon, plus incidental impurities.
  • a concentration of less than about 1 atom percent of Cr, Mo, W, V, Nb, Ta, Ti, Zr and/or Hf does not result in sufficient improvement of the properties of permeability, saturation magnetostriction, coercivity, ac core loss and thermal stability.
  • a concentration o greater than about 6 atom percent of at least one of these elements results in an unacceptably low Curie temperature.
  • the metal content is preferably substantially iron, with up to about 8 atom percent nickel and/or cobalt in order to compensate the reduction of the room temperature saturation magentiza- tion due to the presence of chromium, molybdenum, tungsten, niobium, tantalium, titanium, zirconium and/or hafnium.
  • nickel increases permeability.
  • Examples of metallic glasses of the invention include Fe 80 Ni 1 Mo 1 B 16 Si 2 , Fe 76 Ni 4 Mo 2 B 17.5 Si 0.5 Fe 75 Ni 2 Co 2 Mo 3 B 16 Si 2 , F 75 Co 4 Mo 3 B 16 Si 2 , Fe75Ni4Mo3B16Si2, Fe 77 Ni 2 Mo 3 B 16 Si 2 , Fe 75 Ni 4 Mo 3 B 14 Si 4 , Fe 71 Ni 4 Mo 3 B 17 Si 5 , Fe 74 Ni 4 Mo 4 B 16 Si 2 , Fe 70 Ni 6 Mo 6 B 15 Si 3 , Fe 75 Ni 4 V 3 B 14 Si 2 C 2 , Fe 71 Ni 4 Mo 3 B 16 Si 4 C 2 , Fe78Ni2Mo2B12Si4C2, Fe 78 Ni 2 Cr 2 B 16 Si 2 , Fe 75 Ni 4 Nb 3 B 16 Si 2 , Fe 75 Ni 4 W 3 B 16 Si 2 , Fe75Ni4V3B16Si2' Fe 79 Ni 4 Ta 1 B 16 Si 2 , Fe 75 Ni 4 Ti 3 B 16 Si 2
  • chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and/or hafrium raises the crystallization temperature while simultaneously lowering the Curie temperature of the glassy alloy.
  • the increased separation of these temperatures provides ease of magnetic annealing, that is, thermal annealing at a temperature near the Curie temperature.
  • thermal annealing at a temperature near the Curie temperature.
  • annealing a magnetic material close to its Curie temperature generally results in improved properties.
  • annealing can be easily accomplished at elevated temperatures near the Curie temperature and below the crystallization temperature. Such annealing cannot be carried out for many alloys similar to those of the invention but lacking these elements.
  • too high a concentration of chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and/or hafnium reduces the Curie temperature to a level that may be undesirable in certain applications.
  • chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and/or hafnium concentration is about 2 to 4 atom percent.
  • the metalloid content consist essentially of (1) substantially boron with a small amount of silicon, (2) boron plus silicon and (3) boron and silicon plus a small amount of carbon.
  • the metalloid content ranges from about 17 to 28 atom percent for maximum thermal stability.
  • Preferred metallic glass systems are as follows:
  • Magnetic permeability is the ratio of induction to applied magnetic field. A higher permeability renders a material more useful in certain applications such as tape recorder heads, due to the increased response.
  • the frequency dependence of permeability of the glassy alloys of the invention is similar to that of the 4-79 Permalloys in the medium-to-high frequency range (1-50 kHz), and at higher frequencies (about 50 kHz to 1 MHz), the permeability is comparable to that of the supermalloys.
  • a heat-treated Fe 7s Ni 4 Mo 3 B 16 si 2 metallic glass has permeability of 24,000 while the best-heat-treated prior art Fe40Ni36M04B20 metallic glass has a permeability of 14,000 at 1 kHz and the induction level of 0.01 Tesla.
  • Saturation magnetostriction is the change in length under the influence of a saturating magnetic field.
  • a lower saturation magnetostriction renders a material more useful in certain application such as tape recorder heads.
  • Magnetostriction is usually discussed in terms of the ratio of the change in length to the original length, and is given in ppm.
  • Prior art iron with metallic glasses evidence saturation magnetostric- tions of about 30 ppm as do metallic glasses without the presence of the any of the elements belonging to the IVB, VB and VIB columns of the periodic table such as molybdenum.
  • a prior art iron rich metallic glass designated for use in high frequency applications and having the composition Fe 79 B 16 Si 5 has a saturation magnetostriction of about 30 ppm.
  • a metallic glass of the invention having the composition Fe 75 Ni 4 Mo 3 B 16 Si 2 has a saturation magnetostriction of about 20 ppm.
  • a lower saturation magnetostriction leads to a lower phase angle between the exciting field and the resulting induction. This results in lower exciting power as discussed below.
  • Ac core loss i's that energy loss dissipated as heat. It is the hysteresis in an ac field and is measured by the area of a B-H loop for low frequencies (less than about 1 kHz) and from the complex imput power in the exciting coil for high frequencies (about 1 kHz to 1 MHz).
  • the major portion of the ac core loss at high frequencies arises from the eddy current generated during flux change.
  • a smaller hystersis loss and hence a smaller coercivity is desirable.
  • a lower core loss renders a material more useful in certain applications such as tape recorder heads and transformers. Core loss is discussed in units of watts/kg.
  • Prior art heat-treated metallic glasses typically evidence ac core losses of about 0.05 to 0.1 watts/kg at an induction of 0.1 Tesla and at the frequency range of 1 kHz.
  • a prior art heat-treated metallic glass having the composition Fe40Ni36Mo4B20 has an a c core loss of 0.07 watts/kg at an induction of 0.1 Tesla and at the frequency of 1 kHz
  • a metallic glass having the composition Fe 76 Mo 4 B 20 has an ac core loss of 0.08 watts/kg at an induction of 0.1 Tesla and at the same frequency.
  • a metallic glass alloy of the invention having the composition Fe 75 Ni 4 Mo 3 B 16 Si 2 has an ac core loss of 0.02 watts/kg at an induction of 0.1 Tesla and at the same frequency.
  • Exciting power is a measure of power required to maintain a certain flux density in a magnetic material. It is therefore desirable that a magnetic material to be used in magnetic devices has an exciting power as low as possible.
  • the phase shift is also related to the magnetostriction in such a way that a lower magnetostriction value leads to a lower phase shift. It is then advantageous to have the magnetostriction value as low as possible.
  • prior art iron-rich metallic glasses such as Fe 79 B 16 Si 5 have the magnetostriction value near 30 pp m , in contract to the magnetostriction value of about 20 ppm of the metallic glasses of the present invention.
  • This difference results in a considerable phase shift difference.
  • optimally annealed prior art metallic glass Fe 79 B 16 Si 5 has ⁇ near 70° while the metallic glasses of the present invention have 6 near 50°. This results, for a given core loss, in a higher exciting power by a factor of two for the prior art metallic glass than the metallic glass of the present invention.
  • Crystallization temperature is the temperature at which a metallic glass begins to crystallize. A higher crystallization temperature renders a material more useful in high temperature applications and, in conjunction with a Curie temperature that is substantially lower than the crystallization temperature, permits magnetic annealing just above the Curie temperature. Some metallic glasses crystallize in multiple steps. In such cases, the first crystallization temperature (the lowest value of the crystallization temperatures) is the meaningful one as far as the materials' thermal stability is concerned. The crystallization temperature as discussed herein is measured by differential scanning calorimetry. Prior art glassy alloys evidence crystallization temperatures of about 660 K to 750 K.
  • a metallic glass having the compo- s ition Fe 78 Mo 2 B 20 has a crystallization temperature of 680 K, while a metallic glass having the composition Fe 74 Mo 6 B 20 has a crystallization temperature of 750 K .
  • metallic glasses of the invention evidence increases in crystallization temperatures to a level above 750 K.
  • the magnetic properties of the metallic glasses of the present invention are improved by thermal treatment, characterized by choice of annealing temperatures (T a ), holding time (ta), applied magnetic field (either parallel or perpendicular to the ribbon direction and in the ribbon plane), and post-treatment cooling rate.
  • T a annealing temperatures
  • ta holding time
  • applied magnetic field either parallel or perpendicular to the ribbon direction and in the ribbon plane
  • post-treatment cooling rate post-treatment cooling rate.
  • the optimal properties are obtained after an anneal which causes the controlled precipitation of a certain number of crystalline particles from the glassy matrix. Under these conditions, for compositions having boron content ranging from about 17 to 20 atom percent, the discrete particles have a body-centered cubic structure.
  • the particles are composed essentially of iron, up to 22 atom percent of the iron being adapted to be replaced by at least one of nickel, cobalt, chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium, hafnium, silicon and carbon.
  • the discrete particles consist essentially of a mixture of particles, a major portion of which mixture contains particles having a crystalline Fe 3 B structure.
  • the particles of such portion are composed of iron and boron, up to 14 atom percent of the iron being adapted to be replaced by at least one of nickel, cobalt, chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and hafnium and up to 2 atom percent of the boron being adapted to be replaced by carbon.
  • a small number of such particles introduces a certain decrease in the average domain wall spacing with concomitant decrease in core loss. Too large a number of particles increases the coercivity and thus the hysteresis loss.
  • a metallic glass of the present invention with composition Fe75Ni4Mo3B16Si2 has a combination of low loss and high permeability with a coercivity of only 2 A/m when optimally annealed.
  • an optimally annealed prior art metallic glass Fe79Bl6Sis has a coercivity of about 8 A/m.
  • the crystalline particle size in the optimally heat-treated materials of the present invention ranges between 100 and 300nm, and their volume fraction is less than 1%.
  • the interparticle spacing is of the order of 1-10 ⁇ m.
  • the metallic glasses of the invention have a combination of high permeability, low saturation magnetostriction, low coercivity, low ac core loss, low exciting power and high crystallization temperature and are useful as tape heads, relay cores, transformers and the like.
  • the metallic glasses of the invention are prepared by cooling a melt of the desired composition at a rate of at least about 10 "C/sec, employing quenching techniques well known to the metallic glass art; see e.g., U.S. Patent 3,856,513.
  • the metallic glasses are substantially completely glassy, that is, at least 90% glassy, and consequently possess lower coercivities and are more ductile than less glassy alloys.
  • a variety of techniques are available for fabricating continuous ribbon, wire, sheet, etc. Typically, a particular composition is selected, powders or granules of the requisite elements in the desired portions are melted and homogenized and the molten alloy is rapidly quenched on a chill surface such as a rapidly rotating cylinder.
  • Ribbons having compositions given by Fe 100-a-b-c-d Ni a Mo b B c Si d and having dimensions about 1 to 2.5 cm wide and about 25 to 50 ⁇ m thick were formed by squirting a melt of the particular composition by overpressure of argon onto a rapidly rotating copper chill wheel (surface speed about 3000 to 6000 ft/min).
  • Molybdenum content was varied from 1 to 6 atom percent, for which substantially glassy ribbons were obtained. Molybdenum content higher than 6 atom percent reduced the Curie temperature to an unacceptable low value.
  • Permeability, magnetostriction, core loss, magnetization and coercive force were measured by conventional techniques employing B-H loops, metallic strain gauges and a vibrating sample magnetometer. Curie temperature and crystallization temperature were measured respectively by an induction method and differential scanning calorimetry. The measured values at room temperature saturation induction, Curie temperature, room temperature saturation magnetostriction and the first crystallization temperature are summarized in Table I below. The magnetic properties of these glassy alloys after annealing are presented in Table II. Optimum annealing conditions for the metallic glass Fe 75 Ni 4 Mo 3 B 16 Si 2 and the obtained results are summarized in Table III. Frequency dependence of permability and ac core loss of this optimally annealed alloy are listed in Table IV.
  • the presence of molybdenum is seen to increase the permeability and the crystallization temperature and to lower the ac core loss, exciting power and magnetostriction.
  • the optimally heat-treated metallic glass Fe 7S Ni 4 M0 3 B 16 Si 2 of the present invention has a coercivity reaching as low as 2.5 A/m and yet has a low core loss of 6.5 w/kg and permeability of 12500 at 50 kHz and at the induction level of 0.1 Tesla.
  • the combination of these properties make these compositions suitable for high frequency transformer and tape-head applications.
  • Ribbons having compositions given by Fe 100-a-b-c-d M-M'-B-Si when M is nickel and/or cobalt, M' is one of the elements chromium, molybdenum, tungsten, vanadium, niobium, tantalum, titanium, zirconium and hafnium, and having dimensions about 1 cm wide and about 25 to 50Pm thick were formed as in Example 1.
  • Metal “M'” content was varied from 1 to 6 atom percent, for which substantially glassy ribbons were obtained. Higher metal “M'” content reduced the Curie temperature to an unacceptably low value.
  • a combination of low ac core loss and high permeability at high frequency is achieved in the metallic glasses of the present invention.
  • the thermal stability is also shown to be excellent as evidenced by high crystallization temperature.
  • the metal "M'” content was varied from 1 to 6 atom percent, and the carbon content "e” was up to 2 atom percent for which substantially glassy ribbons were obtained.
  • the metal "M'” content greater than about 6 atom percent reduced the Curie temperature to an unacceptably low value.
  • the magnetic and thermal data are summarized in Table VII below.
  • the magnetic properties of these metallic glasses after annealing are presented in Table VIII.
  • a combination of low ac core loss, high permeability, and high thermal stability of the metallic glasses of the present invention renders these compositions suitable in the magnetic cores of transformers, recording heads and the like.

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  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Mechanical Engineering (AREA)
  • Metallurgy (AREA)
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EP82104504A 1981-08-21 1982-05-24 Alliages vitreux présentant une combinaison de perméabilité élevée, faible champ coercitif, faible perte dans le fer en alternatif, force d'excitation réduite et grande stabilité thermique Expired EP0072893B1 (fr)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
US29516581A 1981-08-21 1981-08-21
US295165 1981-08-21
US31951481A 1981-11-09 1981-11-09
US319514 1981-11-09

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EP0072893A1 true EP0072893A1 (fr) 1983-03-02
EP0072893B1 EP0072893B1 (fr) 1986-12-03

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EP (1) EP0072893B1 (fr)
JP (1) JPH0639663B2 (fr)
KR (1) KR870001283B1 (fr)
AU (1) AU557318B2 (fr)
CA (1) CA1222646A (fr)
DE (1) DE3274562D1 (fr)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0175222A1 (fr) * 1984-09-17 1986-03-26 Energy Conversion Devices, Inc. Procédé pour préparer un aimant dur par l'ajout d'un additif augmentant le domaine de séquence effaçante et aimant dur préparé par ce procédé
US4588452A (en) * 1983-03-16 1986-05-13 Allied Corporation Amorphous alloys for electromagnetic devices
US5160379A (en) * 1986-12-15 1992-11-03 Hitachi Metals, Ltd. Fe-base soft magnetic alloy and method of producing same
US5474624A (en) * 1992-09-14 1995-12-12 Alps Electric Co., Ltd. Method of manufacturing Fe-base soft magnetic alloy
WO1996032518A1 (fr) * 1995-04-13 1996-10-17 Alliedsignal Inc. Alliages amorphes vitreux destines a des systemes de surveillance avec indicateurs a resonance mecanique
US5619174A (en) * 1993-07-30 1997-04-08 Alps Electric Co., Ltd. Noise filter comprising a soft magnetic alloy ribbon core
US6093261A (en) * 1995-04-13 2000-07-25 Alliedsignals Inc. Metallic glass alloys for mechanically resonant marker surveillance systems
US6187112B1 (en) 1995-04-13 2001-02-13 Ryusuke Hasegawa Metallic glass alloys for mechanically resonant marker surveillance systems
EP1848837A2 (fr) * 2005-02-11 2007-10-31 The Nanosteel Company Stabilite de verre amelioree, capacite de formation de verre, et affinage microstructurel
US7935198B2 (en) 2005-02-11 2011-05-03 The Nanosteel Company, Inc. Glass stability, glass forming ability, and microstructural refinement
WO2012010941A1 (fr) 2010-07-21 2012-01-26 Rolex S.A. Composant horloger comprenant un alliage métallique amorphe
WO2012010940A2 (fr) 2010-07-21 2012-01-26 Institut Polytechnique De Grenoble Alliage métallique amorphe
US8704134B2 (en) 2005-02-11 2014-04-22 The Nanosteel Company, Inc. High hardness/high wear resistant iron based weld overlay materials

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4636365B2 (ja) * 2004-07-05 2011-02-23 日立金属株式会社 Fe基非晶質合金薄帯および磁心体
KR100904664B1 (ko) * 2008-06-03 2009-06-25 주식회사 에이엠오 전류 센서용 자기 코어
CA2728346A1 (fr) * 2008-06-16 2010-01-14 The Nanosteel Company, Inc. Verres metalliques ductiles
US11198927B1 (en) * 2019-09-26 2021-12-14 United States Of America As Represented By The Secretary Of The Air Force Niobium alloys for high temperature, structural applications

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4052201A (en) * 1975-06-26 1977-10-04 Allied Chemical Corporation Amorphous alloys with improved resistance to embrittlement upon heat treatment
FR2376217A1 (fr) * 1976-12-29 1978-07-28 Allied Chem Alliages metalliques vitreux ayant une resistance mecanique amelioree
FR2376218A1 (fr) * 1976-12-29 1978-07-28 Allied Chem Verres metalliques vitreux ameliores
DE2806052A1 (de) * 1977-02-18 1978-10-19 Tdk Electronics Co Ltd Thermisch stabile amorphe magnetlegierung
US4140525A (en) * 1978-01-03 1979-02-20 Allied Chemical Corporation Ultra-high strength glassy alloys
DE2855858A1 (de) * 1977-12-28 1979-07-05 Tokyo Shibaura Electric Co Amorphe legierung mit hoher magnetischer permeabilitaet

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4219355A (en) * 1979-05-25 1980-08-26 Allied Chemical Corporation Iron-metalloid amorphous alloys for electromagnetic devices
US4409041A (en) * 1980-09-26 1983-10-11 Allied Corporation Amorphous alloys for electromagnetic devices

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4052201A (en) * 1975-06-26 1977-10-04 Allied Chemical Corporation Amorphous alloys with improved resistance to embrittlement upon heat treatment
FR2376217A1 (fr) * 1976-12-29 1978-07-28 Allied Chem Alliages metalliques vitreux ayant une resistance mecanique amelioree
FR2376218A1 (fr) * 1976-12-29 1978-07-28 Allied Chem Verres metalliques vitreux ameliores
DE2806052A1 (de) * 1977-02-18 1978-10-19 Tdk Electronics Co Ltd Thermisch stabile amorphe magnetlegierung
DE2855858A1 (de) * 1977-12-28 1979-07-05 Tokyo Shibaura Electric Co Amorphe legierung mit hoher magnetischer permeabilitaet
US4140525A (en) * 1978-01-03 1979-02-20 Allied Chemical Corporation Ultra-high strength glassy alloys

Cited By (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4588452A (en) * 1983-03-16 1986-05-13 Allied Corporation Amorphous alloys for electromagnetic devices
EP0175222A1 (fr) * 1984-09-17 1986-03-26 Energy Conversion Devices, Inc. Procédé pour préparer un aimant dur par l'ajout d'un additif augmentant le domaine de séquence effaçante et aimant dur préparé par ce procédé
US5160379A (en) * 1986-12-15 1992-11-03 Hitachi Metals, Ltd. Fe-base soft magnetic alloy and method of producing same
US5474624A (en) * 1992-09-14 1995-12-12 Alps Electric Co., Ltd. Method of manufacturing Fe-base soft magnetic alloy
US5619174A (en) * 1993-07-30 1997-04-08 Alps Electric Co., Ltd. Noise filter comprising a soft magnetic alloy ribbon core
US6187112B1 (en) 1995-04-13 2001-02-13 Ryusuke Hasegawa Metallic glass alloys for mechanically resonant marker surveillance systems
US5628840A (en) * 1995-04-13 1997-05-13 Alliedsignal Inc. Metallic glass alloys for mechanically resonant marker surveillance systems
US6093261A (en) * 1995-04-13 2000-07-25 Alliedsignals Inc. Metallic glass alloys for mechanically resonant marker surveillance systems
WO1996032518A1 (fr) * 1995-04-13 1996-10-17 Alliedsignal Inc. Alliages amorphes vitreux destines a des systemes de surveillance avec indicateurs a resonance mecanique
EP1848837A2 (fr) * 2005-02-11 2007-10-31 The Nanosteel Company Stabilite de verre amelioree, capacite de formation de verre, et affinage microstructurel
EP1848837A4 (fr) * 2005-02-11 2010-02-24 Nanosteel Co Stabilite de verre amelioree, capacite de formation de verre, et affinage microstructurel
US7935198B2 (en) 2005-02-11 2011-05-03 The Nanosteel Company, Inc. Glass stability, glass forming ability, and microstructural refinement
US8704134B2 (en) 2005-02-11 2014-04-22 The Nanosteel Company, Inc. High hardness/high wear resistant iron based weld overlay materials
WO2012010941A1 (fr) 2010-07-21 2012-01-26 Rolex S.A. Composant horloger comprenant un alliage métallique amorphe
WO2012010940A2 (fr) 2010-07-21 2012-01-26 Institut Polytechnique De Grenoble Alliage métallique amorphe
WO2012010940A3 (fr) * 2010-07-21 2012-11-01 Rolex S.A. Alliage métallique amorphe
US9228625B2 (en) 2010-07-21 2016-01-05 Rolex S.A. Amorphous metal alloy
US9315884B2 (en) 2010-07-21 2016-04-19 Rolex Sa Watch-making or clock-making component comprising an amorphous metal alloy

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KR870001283B1 (ko) 1987-06-30
AU557318B2 (en) 1986-12-18
AU8433882A (en) 1983-02-24
EP0072893B1 (fr) 1986-12-03
CA1222646A (fr) 1987-06-09
JPH0639663B2 (ja) 1994-05-25
DE3274562D1 (en) 1987-01-15
JPH04314846A (ja) 1992-11-06
KR840001228A (ko) 1984-03-28

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