EP0080521B1 - Low magnetostriction amorphous metal alloys - Google Patents
Low magnetostriction amorphous metal alloys Download PDFInfo
- Publication number
- EP0080521B1 EP0080521B1 EP81109913A EP81109913A EP0080521B1 EP 0080521 B1 EP0080521 B1 EP 0080521B1 EP 81109913 A EP81109913 A EP 81109913A EP 81109913 A EP81109913 A EP 81109913A EP 0080521 B1 EP0080521 B1 EP 0080521B1
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- European Patent Office
- Prior art keywords
- magnetostriction
- glasses
- alloys
- amorphous metal
- metal alloys
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- 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.)
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- 229910000808 amorphous metal alloy Inorganic materials 0.000 title description 5
- 229910045601 alloy Inorganic materials 0.000 claims description 19
- 239000000956 alloy Substances 0.000 claims description 19
- 239000000203 mixture Substances 0.000 claims description 16
- 229910052804 chromium Inorganic materials 0.000 claims description 12
- 229910052720 vanadium Inorganic materials 0.000 claims description 10
- 229910052796 boron Inorganic materials 0.000 claims description 6
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical group [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims description 3
- 229910001004 magnetic alloy Inorganic materials 0.000 claims description 3
- 239000011521 glass Substances 0.000 description 24
- 239000011651 chromium Substances 0.000 description 12
- 230000005415 magnetization Effects 0.000 description 8
- 239000005300 metallic glass Substances 0.000 description 7
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 6
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 5
- 230000005291 magnetic effect Effects 0.000 description 5
- 238000006467 substitution reaction Methods 0.000 description 5
- 229910017052 cobalt Inorganic materials 0.000 description 4
- 239000010941 cobalt Substances 0.000 description 4
- 229910052748 manganese Inorganic materials 0.000 description 4
- 229910052751 metal Inorganic materials 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- 238000002425 crystallisation Methods 0.000 description 3
- 230000008025 crystallization Effects 0.000 description 3
- 239000000696 magnetic material Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000005259 measurement Methods 0.000 description 3
- 229910052752 metalloid Inorganic materials 0.000 description 3
- 150000002739 metals Chemical class 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- 229910052723 transition metal Inorganic materials 0.000 description 3
- 150000003624 transition metals Chemical class 0.000 description 3
- 230000008901 benefit Effects 0.000 description 2
- 230000008859 change Effects 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000007797 corrosion Effects 0.000 description 2
- 239000002178 crystalline material Substances 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 230000005389 magnetism Effects 0.000 description 2
- 239000000155 melt Substances 0.000 description 2
- 150000002738 metalloids Chemical class 0.000 description 2
- 229910052750 molybdenum Inorganic materials 0.000 description 2
- 229910000889 permalloy Inorganic materials 0.000 description 2
- 229910052710 silicon Inorganic materials 0.000 description 2
- 239000010703 silicon Substances 0.000 description 2
- LEONUFNNVUYDNQ-UHFFFAOYSA-N vanadium atom Chemical compound [V] LEONUFNNVUYDNQ-UHFFFAOYSA-N 0.000 description 2
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- 229910020674 Co—B Inorganic materials 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 238000002441 X-ray diffraction Methods 0.000 description 1
- 238000007792 addition Methods 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 230000005347 demagnetization Effects 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 230000006698 induction Effects 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 229910052753 mercury Inorganic materials 0.000 description 1
- 229910001092 metal group alloy Inorganic materials 0.000 description 1
- 238000000034 method Methods 0.000 description 1
- 229910052758 niobium Inorganic materials 0.000 description 1
- 230000005298 paramagnetic effect Effects 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000035945 sensitivity Effects 0.000 description 1
- HPALAKNZSZLMCH-UHFFFAOYSA-M sodium;chloride;hydrate Chemical compound O.[Na+].[Cl-] HPALAKNZSZLMCH-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 229910052715 tantalum Inorganic materials 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C45/00—Amorphous alloys
- C22C45/04—Amorphous alloys with nickel or cobalt as the major constituent
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01F—MAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
- H01F1/00—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
- H01F1/01—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
- H01F1/03—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
- H01F1/12—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials
- H01F1/14—Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity of soft-magnetic materials metals or alloys
- H01F1/147—Alloys characterised by their composition
- H01F1/153—Amorphous metallic alloys, e.g. glassy metals
- H01F1/15316—Amorphous metallic alloys, e.g. glassy metals based on Co
Definitions
- This invention relates to amorphous metal alloys and, more particularly, to cobalt rich amorphous metal alloys that. include certain transition metal and metalloid elements.
- Metallic glasses generally show resistivities greater than 100 micro ohm cm, whereas crystalline and polycrystalline magnetic metals generally show resistivities below 50 micro ohm cm. Also, because of their randomly disordered structures, metallic glasses are typically isotropic in their physical properties, including their magnetization. Because of these two characteristics, metallic glasses have an initial advantage over conventional magnetic metals. However, metallic glasses do not generally show zero magento- striction. When zero magnetostriction glasses can be found they are generally good soft magnetic metals (R. C. 0'Handley, B. A.
- the EP-A-00 50 479 discloses in Table 1 some amorphous cobalt rich alloys, these alloys contain necessarily silicon. Other cobalt rich amorphous alloys are shown by EP-A-0021 101, but they contain additionally either manganum and silicon or iron. Alloys containing additionally to cobalt and boron only chromium and/or vanadium are not disclosed by both references.
- the present invention provides low magnetostriction and zero magnetostriction glassy alloys that are easy to fabricate and thermally stable.
- the alloys are at least 50 percent glassy and consist essentially of compositions defined by the formula: where T is at least one of Cr and V, B is boron and x ranges from about 0 to 16 atom percent.
- a special magnetic alloy has the composition CO 66 Cr 8 V 6 B 20 .
- the amorphous alloys of the invention can be formed by cooling a melt of the composition at a rate of at least about 10 5 °C/sec.
- a variety of techniques are available, as is now well-known in the art, for fabricating splat-quenched foils and rapid-quenched continuous ribbons, wire, sheet, etc.
- a particular composition is selected, powders of the requisite elements (or of materials that decompose to form the elements, such as nickel-borides, etc.) in the desired proportions are melted and homogenized, and the molten alloy is rapidly quenched either on a chill surface, such as a rotating cooled cylinder, or in a suitable fluid medium, such as a chilled brine solution.
- the amorphous alloys may be formed in air. However, superior mechanical properties are achieved by forming these amorphous alloys in a partial vacuum with absolute pressure less than about 5.5 cm of Hg, and preferably about 100 pm to 1 cm of Hg, as disclosed in U.S. Patent No. 4,154,283 to Ray et al.
- the amorphous metal alloys are at least 50 percent amorphous, and preferably at least 80 percent amorphous, as measured by X-ray diffraction. However, a substantial degree of amorphousness approaching 100 percent amorphous is obtained by forming these amorphous metal alloys in a partial vacuum. Ductility is thereby improved, and such alloys possessing a substantial degree of amorphousness are accordingly preferred.
- Ribbons of these alloys find use in soft magnetic applications and in applications requiring low magnetostriction, high thermal stability (e.g., stable up to about 100°C) and excellent fabricability.
- the magnetostriction measurements were made in fields up to 4 KOe with metal foil strain gauges (as reported in more detail by R. C. O'Handley in Solid State Communications, Vol. 22, p. 485, 1977). The accurary of these measurements is considered to be within 10 percent of full strain and their strain sensitivity is on the order of 10- 7 .
- the trends in Figure 1 reflect the variations of both the saturation moments n B and the Curie temperatures T c of these alloys.
- p x to be the mass density of the crystalline material X and pg to be that of the glassy material X 80 B 20 , the ratios of the measured quantities ⁇ g / ⁇ x were found to be 0.92 and 0.94 for Co 80 B 20 and Fe 80 B 20 glasses.
- the densities of C0 70 X 10 B 20 glasses were calculated by linearly combining the densities of C0 80 B 20 and X s0 B 20 ,
- ⁇ S The temperature dependence of ⁇ S is shown in Figure 4 for selected alloys.
- the sign of ⁇ s was observed to change in two of the glasses.
- Such compensation temperatures have not previously been observed in metallic glasses.
- the vanadium containing glasses either become paramagnetic or they crystallize before any compensation can be realized.
- Co-rich glass compositions with positive and negative magnetostriction can be added linearly to give zero magnetostriction.
- Magnetism and Magnetic Materials are best described by assuming the number of nearest neighbor TM pairs to be independent of x. This implies that the nearest- neighbor coordination of cobalt atoms by cobalt atoms does not vary strongly with x.
- the compositional dependence of magnetostriction in Co-rich glasses is well described at room temperature by: where the first term is the observed two-ion component of magnetostriction (independent of composition x) and the second is the single-ion component of magnetostriction (which varies linearly with the TM concentration).
- the magnetostriction becomes less negative as metalloid content increases, the change in ⁇ being +0.13x 10 -6 per atom percent more metalloid.
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- Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Electromagnetism (AREA)
- Dispersion Chemistry (AREA)
- Power Engineering (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Organic Chemistry (AREA)
- Soft Magnetic Materials (AREA)
Description
- This invention relates to amorphous metal alloys and, more particularly, to cobalt rich amorphous metal alloys that. include certain transition metal and metalloid elements.
- There are three physical parameters which can inhibit the easy magnetization and demagnetization of magnetic materials: strong anistropy, non-zero magnetostriction and, at high frequencies, low resistivity. Metallic glasses generally show resistivities greater than 100 micro ohm cm, whereas crystalline and polycrystalline magnetic metals generally show resistivities below 50 micro ohm cm. Also, because of their randomly disordered structures, metallic glasses are typically isotropic in their physical properties, including their magnetization. Because of these two characteristics, metallic glasses have an initial advantage over conventional magnetic metals. However, metallic glasses do not generally show zero magento- striction. When zero magnetostriction glasses can be found they are generally good soft magnetic metals (R. C. 0'Handley, B. A. Nesbitt, and L. I. Mendelsohn, IEEE Trans Mag-12, p. 942, 1976, U.S. Patents Nos. 4,038,073 and 4,150,981), because they satisfy the three approved criteria. For this reason, interest in zero magnetostriction glasses has been intense as indicated by the many publications on low magnetostriction metallic glasses (A. W. Simpson and W. G. Clements, IEEE Trans Mag-11, p. 1338, 1975; N. Tsuya, K. I. Arai, Y. Shiraga and T. Masumoto, Phys. Lett. A51, p. 121, 1975; H. A. Brooks, Jour. Appl. Phys. 47 p. 334, 1975; T. Egami, P. J. Flanders and C. D. Graham, Jr., Appl. Phys. Lett. 26, p. 128, 1975 and AIP Conf. Proc. No. 24, p. 697, 1975; R. C. Sherwood, E. M. Gyorgy, H. S. Chen, S. D. Ferris, G. Norman and H. J. Leamy, AIP Conf. Proc. No. 24, p. 745,1975; H. Fujimori, K. Arai, H. Shiraga, M. Yamada, T. Masumoto and N. Tsuya, Japan, Jour. Appl. Phys. 15, p. 705,1976; L. Kraus and J. Schneider, Phys Stat. Sol. a39, p. K161, 1977; R. C. O'Handley in Amorphous Magnetism, edited by R. Levy and R. Hasegawa (Plenum Press, New York 1977), p. 379; R. C. O'Handley,-Solid State Communications 21, p. 1119, 1977; R. C. O'Handley, Solid State Communications 22, p. 458, 1977; R. C. O'Handiey, Phys. Rev. 18, p. 930, 1978; H. S. Chen, E. M. Gyorgy, H. J. Leamy and R. C. Sherwood, U.S. Patent No. 4,056,411, Nov. 1, 1977).
- The existence of a zero in the magnetostriction of Co-Mn-B glasses has been observed by H. Hiltzinger of Vacuumschmeltze A. G., Hanau, Germany.
- Reference to Co-rich glasses containing 6 atom percent of Cr is made by N. Heiman, R. D. Hempstead and N. Kazama in Journal of Applied Physics, Vol. 49, p. 5663, 1978. Their interest was in improving the corrosion resistance of Co-B thin films. No reference to magnetostriction is made in that article.
- Saturation moments and Curie temperatures of Co80-xTxP10B10 glasses (T=Mn, Cr, or V) were recently reported by T. Mizoguchi in the Supplement to the Scientific Reports of RITU (Research Institutes of Tonoku University), A June 1978, p. 117. No reference to their magnetostrictive properties was reported.
- In Journal of Applied Physics, Vol. 50, p. 7597, 1979, S. Ohnuma and T. Masumoto outline their studies of magnetization and magnetostriction in Co-Fe-B-Si glasses with light transition metal (Mn, Cr, V, W, Ta, Mo and Nb) substitutions. They show that the coercivity decreases and the effective permeability increases in the composition range near zero magnetostriction.
- The EP-A-00 50 479 discloses in Table 1 some amorphous cobalt rich alloys, these alloys contain necessarily silicon. Other cobalt rich amorphous alloys are shown by EP-A-0021 101, but they contain additionally either manganum and silicon or iron. Alloys containing additionally to cobalt and boron only chromium and/or vanadium are not disclosed by both references.
- New applications requiring improved soft zero- magnetic materials that are easily fabricated and have excellent stability have necessitated efforts to develop further specific compositions.
- The present invention provides low magnetostriction and zero magnetostriction glassy alloys that are easy to fabricate and thermally stable. The alloys are at least 50 percent glassy and consist essentially of compositions defined by the formula:
- A special magnetic alloy has the composition CO66Cr8V6B20.
- The invention will be more fully understood and further advantages will become apparent when reference is made to the following detailed description of the preferred embodiments of the invention and the accompanying drawings, in which
- Figure 1 is a graph showing saturation magnetization for compositions defined by the formula:
- Figure 2 is a graph showing Curie temperatures of compositions for which T is below the crystallization temperature TX;
- Figure 3 is a graph showing the relationships between saturation magnetostriction and composition for selected alloys of the invention;
- Figure 4 is a graph showing the relationships between temperature and magnetostriction values for selected alloys of the invention;
- The amorphous alloys of the invention can be formed by cooling a melt of the composition at a rate of at least about 105°C/sec. A variety of techniques are available, as is now well-known in the art, for fabricating splat-quenched foils and rapid-quenched continuous ribbons, wire, sheet, etc. Typically, a particular composition is selected, powders of the requisite elements (or of materials that decompose to form the elements, such as nickel-borides, etc.) in the desired proportions are melted and homogenized, and the molten alloy is rapidly quenched either on a chill surface, such as a rotating cooled cylinder, or in a suitable fluid medium, such as a chilled brine solution. The amorphous alloys may be formed in air. However, superior mechanical properties are achieved by forming these amorphous alloys in a partial vacuum with absolute pressure less than about 5.5 cm of Hg, and preferably about 100 pm to 1 cm of Hg, as disclosed in U.S. Patent No. 4,154,283 to Ray et al.
- The amorphous metal alloys are at least 50 percent amorphous, and preferably at least 80 percent amorphous, as measured by X-ray diffraction. However, a substantial degree of amorphousness approaching 100 percent amorphous is obtained by forming these amorphous metal alloys in a partial vacuum. Ductility is thereby improved, and such alloys possessing a substantial degree of amorphousness are accordingly preferred.
- Ribbons of these alloys find use in soft magnetic applications and in applications requiring low magnetostriction, high thermal stability (e.g., stable up to about 100°C) and excellent fabricability.
- The following example is presented to provide a more complete understanding of the invention.
- An alloy melt of known composition was rapidly quenched to form non-crystalline ribbons, presumably of the same composition as the melt. The ribbons, typically 40 micrometers (pm) by 2 mm in cross section, were cut into squares for vibration-sample magnetometer measurements of specific magnetization a (4.2K, 9 KOe) and o (T, 9 KOe) with 295 K<T<Tx, the crystallization temperature. Curie temperatures were obtained from the inflection points in the a (T, 9 KOe) curves.
- The magnetostriction measurements were made in fields up to 4 KOe with metal foil strain gauges (as reported in more detail by R. C. O'Handley in Solid State Communications, Vol. 22, p. 485, 1977). The accurary of these measurements is considered to be within 10 percent of full strain and their strain sensitivity is on the order of 10-7.
- Composition variations of the room temperature specific saturation magnetizations a (295 K, 9 KOe) as functions of composition x for CO80-xTxB20 (T=Cr, V) glasses are shown in Figure 1. The trends in Figure 1 reflect the variations of both the saturation moments nB and the Curie temperatures Tc of these alloys.
- The Curie temperatures of Co-rich glasses are generally well above the temperatures for crystallization Tx but fall below T. for sufficiently large additions of Cr or V (Figure 2).
- In order to be useful in magnetic devices, materials should show appreciable magnetization. Commercial zero magnetostriction crystalline metallic alloys of the class exemplified by Permalloy ((Ni82Fe18)1-xXx with x=Mo or Cu and x<.04) have saturation inductions
- Defining px to be the mass density of the crystalline material X and pg to be that of the glassy material X80B20, the ratios of the measured quantities ρg/ρx were found to be 0.92 and 0.94 for Co80B20 and Fe80B20 glasses. A similar trend holds for the hypothetical X80B20 glasses listed in Table I. The estimated densities of X80B20 (X=Mn, Cr, V) glasses are also set forth in Table I. The densities of C070X10B20 glasses were calculated by linearly combining the densities of C080B20 and Xs0B20,
- In Figure 3, there is shown the effects of Cr and V substitutions on the saturation magnetostriction of Co80B20 glass. As is the case with the Fe substitutions for Co disclosed by U.S. Patent No. 4,038,073 to O'Handley et al., the lighter transition metals cause λs to increase through zero, positive below Tc for Mn and Cr substitutions and go to zero for V substitutions. In the case of Co66V14B20 glass, Tc=300 K (Fig. 2). Thus, the room temperature magnetostriction is zero probably because of the low Tc. Co80-xVxB20 glasses with x>14 may show positive magnetostriction at 4.2 K (see Fig. 4). These Co-Cr-B glasses are, therefore, non-magnetostrictive alloys.
- The temperature dependence of λS is shown in Figure 4 for selected alloys. The sign of Às was observed to change in two of the glasses. Such compensation temperatures have not previously been observed in metallic glasses. The vanadium containing glasses either become paramagnetic or they crystallize before any compensation can be realized. Thus, the negative magnetostriction glasses shown in Figure 3 may be used in applications requiring as=0 at some elevated temperature (up to approximately 200°C above room temperature, which is not uncommon in many electronic devices).
- The new low magnetostriction metallic glasses disclosed herein (Co-Cr-B and Co-V-B) show relatively low 4nMs (Fig. 1). As a result, their utility is limited to applications requiring superior mechanical properties or improved corrosion resistance relative to permalloys or other λs=0 crystalline or non-crystalline materials.
- Co-rich glass compositions with positive and negative magnetostriction can be added linearly to give zero magnetostriction.
- The rule of linear combination of opposing magnetostrictions (LCOM) has been applied to develop additional zero magnetostriction glasses from those measured and shown in Figure 3.
- The magnetostriction of Co-rich glasses is small because of the near-cancellation of two independent mechanisms for the magnetostriction, a positive two-ion interaction and a negative single-TM-ion term (O'Handley, Phys. Rev. B 18, p. 930, 1978). As a result, the TM makeup for λs=O is nearly independent of TM/M ratio. That is, because λs=0 for observed trends in C0100-xB. glasses (K. Narita, J. Yamasaki, and H. Fukunaga, Jour. Appl. Phys. Vol. 50, p. 7591, 1979 and J. Aboaf and B. Klokholm, ICM Munich Sept. 1979 to appear in Jour. Magnetism and Magnetic Materials), are best described by assuming the number of nearest neighbor TM pairs to be independent of x. This implies that the nearest- neighbor coordination of cobalt atoms by cobalt atoms does not vary strongly with x. Thus the compositional dependence of magnetostriction in Co-rich glasses is well described at room temperature by:
Claims (2)
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP81109913A EP0080521B1 (en) | 1981-11-26 | 1981-11-26 | Low magnetostriction amorphous metal alloys |
DE8181109913T DE3175475D1 (en) | 1981-11-26 | 1981-11-26 | Low magnetostriction amorphous metal alloys |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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EP81109913A EP0080521B1 (en) | 1981-11-26 | 1981-11-26 | Low magnetostriction amorphous metal alloys |
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EP85101588.3 Division-Into | 1981-11-26 | ||
EP85101590.9 Division-Into | 1981-11-26 | ||
EP85101589.1 Division-Into | 1981-11-26 |
Publications (2)
Publication Number | Publication Date |
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EP0080521A1 EP0080521A1 (en) | 1983-06-08 |
EP0080521B1 true EP0080521B1 (en) | 1986-10-15 |
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EP81109913A Expired EP0080521B1 (en) | 1981-11-26 | 1981-11-26 | Low magnetostriction amorphous metal alloys |
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EP (1) | EP0080521B1 (en) |
DE (1) | DE3175475D1 (en) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
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US4439253A (en) * | 1982-03-04 | 1984-03-27 | Allied Corporation | Cobalt rich manganese containing near-zero magnetostrictive metallic glasses having high saturation induction |
DE69013642T2 (en) * | 1989-11-17 | 1995-03-02 | Hitachi Metals Ltd | Magnetic alloy with ultra-small crystal grains and manufacturing process. |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0050479A1 (en) * | 1980-10-16 | 1982-04-28 | Unitika Ltd. | Amorphous co-based metal filaments and process for the production of the same |
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US4056411A (en) * | 1976-05-14 | 1977-11-01 | Ho Sou Chen | Method of making magnetic devices including amorphous alloys |
DE2824749A1 (en) * | 1978-06-06 | 1979-12-13 | Vacuumschmelze Gmbh | INDUCTIVE COMPONENT AND PROCESS FOR ITS MANUFACTURING |
DE2924280A1 (en) * | 1979-06-15 | 1981-01-08 | Vacuumschmelze Gmbh | AMORPHE SOFT MAGNETIC ALLOY |
-
1981
- 1981-11-26 EP EP81109913A patent/EP0080521B1/en not_active Expired
- 1981-11-26 DE DE8181109913T patent/DE3175475D1/en not_active Expired
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EP0050479A1 (en) * | 1980-10-16 | 1982-04-28 | Unitika Ltd. | Amorphous co-based metal filaments and process for the production of the same |
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EP0080521A1 (en) | 1983-06-08 |
DE3175475D1 (en) | 1986-11-20 |
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