EP0575190A2 - Fe-base soft magnetic alloy and process for making same - Google Patents
Fe-base soft magnetic alloy and process for making same Download PDFInfo
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- EP0575190A2 EP0575190A2 EP93304762A EP93304762A EP0575190A2 EP 0575190 A2 EP0575190 A2 EP 0575190A2 EP 93304762 A EP93304762 A EP 93304762A EP 93304762 A EP93304762 A EP 93304762A EP 0575190 A2 EP0575190 A2 EP 0575190A2
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- 229910001004 magnetic alloy Inorganic materials 0.000 title claims abstract description 27
- 238000000034 method Methods 0.000 title claims description 13
- 239000000956 alloy Substances 0.000 claims abstract description 57
- 229910045601 alloy Inorganic materials 0.000 claims abstract description 56
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims abstract description 24
- 229910052742 iron Inorganic materials 0.000 claims abstract description 9
- 239000000203 mixture Substances 0.000 claims abstract description 7
- 229910052726 zirconium Inorganic materials 0.000 claims abstract description 6
- 229910052684 Cerium Inorganic materials 0.000 claims abstract description 5
- 229910052782 aluminium Inorganic materials 0.000 claims abstract description 5
- 229910052787 antimony Inorganic materials 0.000 claims abstract description 5
- 229910052804 chromium Inorganic materials 0.000 claims abstract description 5
- 229910052733 gallium Inorganic materials 0.000 claims abstract description 5
- 229910052732 germanium Inorganic materials 0.000 claims abstract description 5
- 229910052735 hafnium Inorganic materials 0.000 claims abstract description 5
- 229910052748 manganese Inorganic materials 0.000 claims abstract description 5
- 229910052750 molybdenum Inorganic materials 0.000 claims abstract description 5
- 229910052759 nickel Inorganic materials 0.000 claims abstract description 5
- 229910052758 niobium Inorganic materials 0.000 claims abstract description 5
- 229910052763 palladium Inorganic materials 0.000 claims abstract description 5
- 229910052707 ruthenium Inorganic materials 0.000 claims abstract description 5
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 5
- 229910052715 tantalum Inorganic materials 0.000 claims abstract description 5
- 229910052718 tin Inorganic materials 0.000 claims abstract description 5
- 229910052719 titanium Inorganic materials 0.000 claims abstract description 5
- 229910052721 tungsten Inorganic materials 0.000 claims abstract description 5
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 5
- 229910052727 yttrium Inorganic materials 0.000 claims abstract description 5
- 239000002245 particle Substances 0.000 claims description 22
- 238000010438 heat treatment Methods 0.000 claims description 12
- 239000010409 thin film Substances 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 3
- 239000006104 solid solution Substances 0.000 claims description 3
- 238000007578 melt-quenching technique Methods 0.000 claims description 2
- 238000002441 X-ray diffraction Methods 0.000 description 8
- 239000010949 copper Substances 0.000 description 8
- 239000013078 crystal Substances 0.000 description 7
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 6
- 230000035699 permeability Effects 0.000 description 6
- 238000005096 rolling process Methods 0.000 description 5
- 239000007789 gas Substances 0.000 description 4
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 3
- 229910000808 amorphous metal alloy Inorganic materials 0.000 description 3
- 229910052786 argon Inorganic materials 0.000 description 3
- 229910052796 boron Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
- 239000011162 core material Substances 0.000 description 3
- 239000000696 magnetic material Substances 0.000 description 3
- 230000005415 magnetization Effects 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 2
- 229910052802 copper Inorganic materials 0.000 description 2
- 238000002425 crystallisation Methods 0.000 description 2
- 230000008025 crystallization Effects 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 230000004907 flux Effects 0.000 description 2
- 239000011261 inert gas Substances 0.000 description 2
- 239000005300 metallic glass Substances 0.000 description 2
- 238000010791 quenching Methods 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 239000012535 impurity Substances 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 238000005551 mechanical alloying Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 229910052698 phosphorus Inorganic materials 0.000 description 1
- 230000000171 quenching effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 238000004544 sputter deposition Methods 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 238000007740 vapor deposition Methods 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
- C22C45/02—Amorphous alloys with iron 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
- H01F1/032—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 hard-magnetic materials
- H01F1/04—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 hard-magnetic materials metals or alloys
-
- 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
- H01F1/15308—Amorphous metallic alloys, e.g. glassy metals based on Fe/Ni
Definitions
- the present invention relates to an Fe-base soft magnetic alloy and, in particular, to an alloy having excellent soft magnetic properties and a process for making it.
- Fe-base amorphous magnetic alloys having a high saturation magnetic flux density are known to be used as magnetic core materials for magnetic heads, high frequency transformers, saturable reactors, choke coils, etc.
- Fe-base amorphous magnetic alloys are lower priced than Co-base ones, the former have the drawbacks of large core loss in high frequency region and a low permeability.
- it's saturation magnetostriction is high.
- An Fe-B system alloy is known as conventional Fe-system amorphous magnetic alloys.
- the alloys including B (boron) are high priced because the element B is expensive.
- One object of the present invention is to provide a novel Fe-base soft magnetic alloy, which can be substituted for the above-mentioned conventional soft magnetic materials and has a low saturation magnetostriction and a low iron loss.
- Another object of the present invention is to provide an Fe-base soft magnetic alloy which is lower priced.
- an Fe-base soft magnetic alloy which has a composition represented by the formula: Fe 100-a-b-c-d P a M b M' c Cu d
- M is at least one element selected from the group consisting of Zr, Hf, Nb, Mo, W, Ta, Ti, V, Cr, Mn, Y and Ce
- M' is at least one element selected from the group consisting of Si, Al, Ga, Ge, Ru, Co, Ni, Sn, Sb and Pd
- a, b, c and d each are an atomic % (atom %) and each satisfy 0 ⁇ a ⁇ 25, 0 ⁇ b ⁇ 15, 0 ⁇ c ⁇ 20, and 0 ⁇ d ⁇ 5.
- at least 30 % of the alloy structure is desired to be occupied by fine crystalline particles, and the crystalline particles are desired to be composed of bcc solid solution including mainly Fe.
- P phosphorous
- a determined amount of P enables to extend the range of formation of amorphous alloys after quenching without using an expensive element B (boron). Thereby, the cost of preparation of the alloy can be reduced.
- the content (a) of P is more than 0 atomic % and not more than 25 atomic %, preferably from 1 to 15 atomic %, more preferably from 2 to 12 atomic %.
- the element(s) M added to the Fe-base soft magnetic alloy of the present invention is supposed to prevent crystallization of the Fe-P system crystal which hampers soft magnetic properties of the alloy or to elevate its crystallization temperature.
- M is mentioned at least one, i.e. one or more of the elements selected from the group consisting of Zr, Hf, Nb, Mo, W, Ta, Ti, V, Cr, Mn, Y and Ce. Particularly Zr is preferable. Addition of the element(s) M is further effective for making the crystal grain fine and for improving the ability of forming the amorphous phase of the alloy in the Fe-P system alloy.
- the content (b) of the M element(s) is more than 0 atomic % and not more than 15 atomic %, preferably from 2 to 15 atomic %, more preferably from 3 to 12 atomic %.
- the element(s) M' added to the Fe-base soft magnetic alloy of the present invention is one or more of the elements selected from the group consisting of Si, Al, Ga, Ge, Ru, Co, Ni, Sn, Sb and Pd. It is considered that these elements are dissolved in the Fe-major solid solution because they have a negative interaction parameter relative to Fe, that is, it is considered that the elements are dissolved as being substituted for Fe atom in the a-Fe crystalline structure whereby stabilizes the bcc crystal. Thus, it is considered that the crystalline grain having a genuine magnetocrystalline anisotropy of bcc crystalline or low magnetostriction constant is formed to exhibit excellent soft magnetic properties.
- the content (c) of the M' element(s) is from 0 atomic % to 20 atomic %, preferably from 1 to 15 atomic %.
- Cu (copper) in the alloy of the present invention is effective for making the crystalline particles obtained by the heat-treatment of the amorphous fine. Further, it improves the magnetic properties of the alloy since the effective magnetic anisotropy energy becomes smaller than its genuine magnetocrystalline anisotropy energy as the particles become fine.
- the copper content should not be more than 5 atomic % with respect to the preparation of the alloy because the just quenched alloy tends to be brittle. Accordingly, the content (d) of Cu is from 0 to 5 atomic %, preferably from 0.5 to 3 atomic %.
- alloy further containing inevitable impurities such as N, S, O etc., to the extent that these element do not deteriorate the properties of the alloy, is also included in the scope of the present invention.
- the Fe-base soft magnetic alloy according to the present invention has an alloy structure, at least 30 % (30 % - 100 %) of which consists of (is composed of) fine crystalline particles, with the balance of the structure being an amorphous phase or other crystals than above-mentioned fine crystalline particles.
- the range of the ratio of the fine crystalline particles in the structure provides the alloy excellent (soft) magnetic properties.
- the alloy has yet sufficiently good magnetic properties.
- at least 50 %, more preferably 70 % or more of the alloy structure consists of (is composed of) the fine crystalline particles in view of magnetic properties.
- the crystalline particles of the alloy of the present invention has mainly a bcc structure and it is considered that Fe as a main component and M, M' and a small amount of P are believed to be dissolved in.
- the crystalline particles to be formed in the alloy of the present invention have a particle size of 1000 ⁇ or less, preferably 500 ⁇ or less, more preferably 50 to 300 ⁇ .
- the particle size being 1000 ⁇ or less, preferably 500 ⁇ or less, more preferably 50 to 300 ⁇ , provides the alloy of the present invention excellent magnetic properties.
- the proportion of the crystalline grains to the total alloy structure in the alloy of the present invention may be determined experimentally by an X-ray diffraction method or the like. Briefly, on the basis of the standard value of the X-ray diffraction intensity of Fe-base crystal in the completely crystallized condition (saturated X-ray diffraction intensity condition), the proportion of the X-ray diffraction intensity of the magnetic alloy material sample to be examined to the standard value may be obtained experimentally.
- the Fe-base soft magnetic alloy of the present invention may be produced by a heat-treatment of an amorphous metal having a determined shape which is obtained by a common method of forming an amorphous metal.
- an amorphous alloy is first formed in the form of a ribbon, powder, fiber, or thin film by a melt quenching method such as a single roll method or double roll method, a thin film forming method such as a cavitation method, sputtering method or vapor deposition method, or a powder forming method such as mechanical alloying or the like.
- the resulting amorphous alloy is optionally shaped and worked into a desired shape, then it is heat-treated so that at least a part, preferably 30 % or more of the whole, of the sample is crystallized to obtain the alloy of the present invention.
- the structure of the alloy after rapid-quenching is preferably amorphous but it may include partially crystal to the extent that the resulting alloy exhibits soft magnetic properties after heat-treatment.
- a quenched alloy ribbon is formed by a single roll method, and this is shaped into a determined shape such as a coiled magnetic core and then heat-treated.
- the heat-treatment is effected in vacuum, in an inert gas atmosphere, such as an argon gas or nitrogen gas atmosphere, in reducing gas atmosphere such as H2 or in oxidizing gas atmosphere such as air. Preferably, it is carried out in vacuum or in an inert gas atmosphere.
- the heat-treatment temperature is approximately from 200 to 800°C, preferably approximately from 300 to 700°C, and more preferably from 400 to 700 °C.
- the heat-treatment time is within 24 hours, preferably about from 0.5 to 5 hours.
- the heat-treatment may be effected either in the absence or presence of a magnetic field. Impressing of a magnetic field brings a magnetic anisotropy to the alloy.
- the soft magnetic alloy having excellent properties is obtained.
- Fig. 1 is a graph showing X-ray diffraction patterns of the Fe-base soft magnetic alloy of the present invention after heat-treatment.
- a quenched ribbon (thin film) sample having a width of about 1.5 mm and a thickness of about 15-24 ⁇ m was formed from a melt containing Fe, P, Zr, and (Cu) in an argon gas atmosphere of one atmosphere pressure by a single roll method.
- the sample was then heat-treated at the temperature shown by Table 1 for about one hour in the presence of a nitrogen gas and in the absence of a magnetic field.
- the iron loss (Pc W/kg) of each of the samples was determined under the condition of a frequency of 100 kHz and a maximum magnetic flux density of 0.1 T.
- the permeability ( ⁇ ) (1KHz) under the condition of a frequency of 1 kHz and a maximum exciting magnetic field of 5 mOe, the saturation magnetization Ms (emu/g) and the saturation magnetostriction constant ⁇ s ( ⁇ 10 ⁇ 6) of each samples were also determined.
- the composition of the alloy samples, the content of the fine crystalline particles in the alloy and the average particle size are shown in Table 1 below.
- Table 1 Composition of Alloy (atomic %) Temperature of heat-treatment(°C) Content of crystalline particle(%) Particle size of Crystal ( ⁇ ) Exam.1 Fe89Zr9P2 620 60 or more - Exam.2 Fe85Zr9P6 620 60 or more - Exam.3 Fe88Zr9P2Cu1 620 60 or more 170 Comp. Exam. Fe78Si9B13 410 - -
- the content of the fine crystalline particles is 60 % or more in all of the samples.
- the composition of the alloy was determined by IPC analysis.
- Fig. 1 shows the X-ray diffraction curves of the alloy of Fe88Zr9P2Cu1 (atomic %)(Example 3) obtained by heat-treating the quenched alloy formed by a single roll method, at 620 °C in the presense of argon for one hour.
- the structure of the alloy obtained by heat-treatment has mainly bcc structure.
- the Fe-base soft magnetic alloy of the present invention shows an excellent magnetic properties such as low ion loss, high permeability and low saturation magnetsrtiction by adding specific element(s), particularly Zr together with Cu to Fe-P system alloy. Accordingly, the alloy of the present invention can be utilized widely for a magnetic head, high-frequency transformers, saturable reactors, choke coils and like as the magnetic material substitited for the Fe-B system soft magnetic alloy.
- the Fe-base soft magnetic alloy of the present invention can be reduce the cost of the preparation of the alloy since it utilizes phosphor P instead of boron B.
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Abstract
a, b, c and d each are an atomic % and satisfy the relations: 0 < a ≦ 25, 0 < b ≦ 15, 0 ≦ c ≦ 20, and 0 ≦ d ≦ 5 having excellent soft magnetic properties, especially low magnetostriction and low iron loss is made by adding a determined amount of a specific element M, a determined amount of Cu is further added to the alloy and the quenched alloy composition is shaped and heat-treated to provide the Fe-base soft magnetic alloy.
Description
- The present invention relates to an Fe-base soft magnetic alloy and, in particular, to an alloy having excellent soft magnetic properties and a process for making it.
- Fe-base amorphous magnetic alloys having a high saturation magnetic flux density are known to be used as magnetic core materials for magnetic heads, high frequency transformers, saturable reactors, choke coils, etc. However, though Fe-base amorphous magnetic alloys are lower priced than Co-base ones, the former have the drawbacks of large core loss in high frequency region and a low permeability. In addition, it's saturation magnetostriction is high.
- An Fe-B system alloy is known as conventional Fe-system amorphous magnetic alloys. However, the alloys including B (boron) are high priced because the element B is expensive.
- One object of the present invention is to provide a novel Fe-base soft magnetic alloy, which can be substituted for the above-mentioned conventional soft magnetic materials and has a low saturation magnetostriction and a low iron loss.
- Another object of the present invention is to provide an Fe-base soft magnetic alloy which is lower priced.
- Intense researches and studies of various Fe-base soft magnetic alloys in view of the above objects have revealed that addition of specific element(s) M, particularly Zr, to an Fe-P system Fe-base soft magnetic alloy can provide an improved Fe-base Fe-Si-B-Al soft magnetic alloy having excellent soft magnetic characteristics, for example, having an extremely low saturation magnetostriction, and that addition of Cu to the Fe-P-M system Fe-base soft magnetic alloy is effective for obtaining excellent soft magnetic properties of the resulting alloy. The present invention is based on these findings.
- Specifically, there is provided in accordance with the present invention an Fe-base soft magnetic alloy which has a composition represented by the formula:
where M is at least one element selected from the group consisting of Zr, Hf, Nb, Mo, W, Ta, Ti, V, Cr, Mn, Y and Ce;
M' is at least one element selected from the group consisting of Si, Al, Ga, Ge, Ru, Co, Ni, Sn, Sb and Pd;
a, b, c and d each are an atomic % (atom %) and each satisfy 0 < a ≦ 25, 0 < b ≦ 15, 0 ≦ c ≦ 20, and 0 ≦ d ≦ 5. In particular, at least 30 % of the alloy structure is desired to be occupied by fine crystalline particles, and the crystalline particles are desired to be composed of bcc solid solution including mainly Fe. - P (phosphorous) is an essential element of constituting the alloy of the present invention and addition of a determined amount of P (more than 0 atomic % and not more than 25 atomic %) enables to extend the range of formation of amorphous alloys after quenching without using an expensive element B (boron). Thereby, the cost of preparation of the alloy can be reduced.
- The content (a) of P is more than 0 atomic % and not more than 25 atomic %, preferably from 1 to 15 atomic %, more preferably from 2 to 12 atomic %.
- The element(s) M added to the Fe-base soft magnetic alloy of the present invention is supposed to prevent crystallization of the Fe-P system crystal which hampers soft magnetic properties of the alloy or to elevate its crystallization temperature. As M is mentioned at least one, i.e. one or more of the elements selected from the group consisting of Zr, Hf, Nb, Mo, W, Ta, Ti, V, Cr, Mn, Y and Ce. Particularly Zr is preferable. Addition of the element(s) M is further effective for making the crystal grain fine and for improving the ability of forming the amorphous phase of the alloy in the Fe-P system alloy.
- The content (b) of the M element(s) is more than 0 atomic % and not more than 15 atomic %, preferably from 2 to 15 atomic %, more preferably from 3 to 12 atomic %.
- The element(s) M' added to the Fe-base soft magnetic alloy of the present invention is one or more of the elements selected from the group consisting of Si, Al, Ga, Ge, Ru, Co, Ni, Sn, Sb and Pd. It is considered that these elements are dissolved in the Fe-major solid solution because they have a negative interaction parameter relative to Fe, that is, it is considered that the elements are dissolved as being substituted for Fe atom in the a-Fe crystalline structure whereby stabilizes the bcc crystal. Thus, it is considered that the crystalline grain having a genuine magnetocrystalline anisotropy of bcc crystalline or low magnetostriction constant is formed to exhibit excellent soft magnetic properties.
- The content (c) of the M' element(s) is from 0 atomic % to 20 atomic %, preferably from 1 to 15 atomic %.
- Cu (copper) in the alloy of the present invention is effective for making the crystalline particles obtained by the heat-treatment of the amorphous fine. Further, it improves the magnetic properties of the alloy since the effective magnetic anisotropy energy becomes smaller than its genuine magnetocrystalline anisotropy energy as the particles become fine. However, the copper content should not be more than 5 atomic % with respect to the preparation of the alloy because the just quenched alloy tends to be brittle. Accordingly, the content (d) of Cu is from 0 to 5 atomic %, preferably from 0.5 to 3 atomic %.
- Incidentally, alloy further containing inevitable impurities such as N, S, O etc., to the extent that these element do not deteriorate the properties of the alloy, is also included in the scope of the present invention.
- The Fe-base soft magnetic alloy according to the present invention has an alloy structure, at least 30 % (30 % - 100 %) of which consists of (is composed of) fine crystalline particles, with the balance of the structure being an amorphous phase or other crystals than above-mentioned fine crystalline particles. The range of the ratio of the fine crystalline particles in the structure provides the alloy excellent (soft) magnetic properties. In the present invention, even if the crystalline particles occupy substantially 100 % of the structure, the alloy has yet sufficiently good magnetic properties. Preferably at least 50 %, more preferably 70 % or more of the alloy structure consists of (is composed of) the fine crystalline particles in view of magnetic properties.
- The crystalline particles of the alloy of the present invention has mainly a bcc structure and it is considered that Fe as a main component and M, M' and a small amount of P are believed to be dissolved in.
- It is preferred that the crystalline particles to be formed in the alloy of the present invention have a particle size of 1000 Å or less, preferably 500 Å or less, more preferably 50 to 300 Å. The particle size being 1000 Å or less, preferably 500Å or less, more preferably 50 to 300 Å, provides the alloy of the present invention excellent magnetic properties.
- The proportion of the crystalline grains to the total alloy structure in the alloy of the present invention may be determined experimentally by an X-ray diffraction method or the like. Briefly, on the basis of the standard value of the X-ray diffraction intensity of Fe-base crystal in the completely crystallized condition (saturated X-ray diffraction intensity condition), the proportion of the X-ray diffraction intensity of the magnetic alloy material sample to be examined to the standard value may be obtained experimentally.
- The average size of the crystalline particles is determined from Scheller's equation (t=0.9λ/β·cosϑ) by using bcc peak reflection of the X-ray diffraction pattern (Element of X-ray Diffraction (Second Edition), pages 91-94, B.D. Cullity).
- The Fe-base soft magnetic alloy of the present invention may be produced by a heat-treatment of an amorphous metal having a determined shape which is obtained by a common method of forming an amorphous metal. For instance, an amorphous alloy is first formed in the form of a ribbon, powder, fiber, or thin film by a melt quenching method such as a single roll method or double roll method, a thin film forming method such as a cavitation method, sputtering method or vapor deposition method, or a powder forming method such as mechanical alloying or the like. The resulting amorphous alloy is optionally shaped and worked into a desired shape, then it is heat-treated so that at least a part, preferably 30 % or more of the whole, of the sample is crystallized to obtain the alloy of the present invention.
- The structure of the alloy after rapid-quenching is preferably amorphous but it may include partially crystal to the extent that the resulting alloy exhibits soft magnetic properties after heat-treatment.
- Generally, a quenched alloy ribbon is formed by a single roll method, and this is shaped into a determined shape such as a coiled magnetic core and then heat-treated. The heat-treatment is effected in vacuum, in an inert gas atmosphere, such as an argon gas or nitrogen gas atmosphere, in reducing gas atmosphere such as H₂ or in oxidizing gas atmosphere such as air. Preferably, it is carried out in vacuum or in an inert gas atmosphere. The heat-treatment temperature is approximately from 200 to 800°C, preferably approximately from 300 to 700°C, and more preferably from 400 to 700 °C. The heat-treatment time is within 24 hours, preferably about from 0.5 to 5 hours. The heat-treatment may be effected either in the absence or presence of a magnetic field. Impressing of a magnetic field brings a magnetic anisotropy to the alloy.
- By the heat treatment of the amorphous alloy being carried out in the aforementioned range of temperature and within the aforementioned time range, the soft magnetic alloy having excellent properties is obtained.
- Fig. 1 is a graph showing X-ray diffraction patterns of the Fe-base soft magnetic alloy of the present invention after heat-treatment.
- Examples of the present invention are described hereinafter.
- A quenched ribbon (thin film) sample having a width of about 1.5 mm and a thickness of about 15-24 µm was formed from a melt containing Fe, P, Zr, and (Cu) in an argon gas atmosphere of one atmosphere pressure by a single roll method. The sample was then heat-treated at the temperature shown by Table 1 for about one hour in the presence of a nitrogen gas and in the absence of a magnetic field.
- The iron loss (Pc W/kg) of each of the samples was determined under the condition of a frequency of 100 kHz and a maximum magnetic flux density of 0.1 T. The permeability (µ) (1KHz) under the condition of a frequency of 1 kHz and a maximum exciting magnetic field of 5 mOe, the saturation magnetization Ms (emu/g) and the saturation magnetostriction constant λs (×10⁻⁶) of each samples were also determined. The composition of the alloy samples, the content of the fine crystalline particles in the alloy and the average particle size are shown in Table 1 below.
Table 1 Composition of Alloy (atomic %) Temperature of heat-treatment(°C) Content of crystalline particle(%) Particle size of Crystal (Å) Exam.1 Fe₈₉Zr₉P₂ 620 60 or more - Exam.2 Fe₈₅Zr₉P₆ 620 60 or more - Exam.3 Fe₈₈Zr₉P₂Cu₁ 620 60 or more 170 Comp. Exam. Fe₇₈Si₉B₁₃ 410 - - - As shown by Table 1, the content of the fine crystalline particles is 60 % or more in all of the samples. The composition of the alloy was determined by IPC analysis.
- The magnetic properties are shown in Table 2.
- As comparative samples, a rapid quenched alloy of Fe₇₈Si₉B₁₃ (Comparative Example, commercial product) was prepared as in the same condition as the example 1, and the iron loss, permeability, saturation magnetization and saturation magnetostriction of these samples were also shown in Table 2 below.
Table 2 Iron Loss (Pc.CW/kg) Permeability (µ, 1kHz) Saturation Magnetization (Ms,emu/g) Saturation Magnetostrication (×10⁻⁶) Exam.1 50 3400 - - Exam.2 35 4700 - - Exam.3 30 8000 - -0.6 Comp. Exam. 40 5600 170 28 - As is obvious from the results in Table 2 above, the iron loss and the permeability of the alloy samples of the present invention are almost the same as those of the sample of Comparative Example and the ally of the present invention is found to be sufficiently practical for the magnetic material substituted for the Fe-B amorphous soft magnetic alloy.
- Fig. 1 shows the X-ray diffraction curves of the alloy of Fe₈₈Zr₉P₂Cu₁ (atomic %)(Example 3) obtained by heat-treating the quenched alloy formed by a single roll method, at 620 °C in the presense of argon for one hour. As is obvious from the figure, the structure of the alloy obtained by heat-treatment has mainly bcc structure.
- As is obvious from the results in the above-mentioned examples, the Fe-base soft magnetic alloy of the present invention shows an excellent magnetic properties such as low ion loss, high permeability and low saturation magnetsrtiction by adding specific element(s), particularly Zr together with Cu to Fe-P system alloy. Accordingly, the alloy of the present invention can be utilized widely for a magnetic head, high-frequency transformers, saturable reactors, choke coils and like as the magnetic material substitited for the Fe-B system soft magnetic alloy.
- In addition, the Fe-base soft magnetic alloy of the present invention can be reduce the cost of the preparation of the alloy since it utilizes phosphor P instead of boron B.
Claims (9)
- An Fe-base soft magnetic alloy having a composition of formula:
a, b, c and d each are an atomic % and satisfy the relations: 0 < a ≦ 25, 0 < b ≦ 15, 0 ≦ c ≦ 20, and 0 ≦ d ≦ 5. - An alloy according to claim 1 in which at least 30% of the alloy structure is occupied by fine crystalline particles.
- An alloy acording to claim 2 in which the crystalline particle is a bcc solid solution including mainly iron.
- An alloy according to any one of claims 1 to 3 in which the average size of the particles is not more than 100nm.
- An alloy according to any one of claims 1 to 4 in which the saturation magnetostriction (λs) of the alloy is from +10 x 10⁻⁶ to -5 x 10⁻⁶.
- A process for making an Fe-base soft magnetic alloy comprising
forming a quenched alloy having a composition of formula
0 < a ≦ 25, 0 < b ≦ 15, 0 ≦ c ≦ 20, and 0 ≦ d ≦ 5,
by a melt quenching method, a thin film forming method or a powder forming method and treating the quenched alloy by heat. - A process according to claim 6 in which the quenched alloy is maintained at the temperature from 350 °C to 700 °C for less than 24 hours during heat-treatment.
- A process according to claim 6 or claim 7 for producing an alloy according to any one of claims 2 to 5.
- A magnetic core consisting of an alloy according to any one of claims 1 to 5 or produced according to claim 6 or claim 7.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15833892A JP3623970B2 (en) | 1992-06-17 | 1992-06-17 | Fe-based soft magnetic alloy and manufacturing method |
JP158338/92 | 1992-06-17 |
Publications (3)
Publication Number | Publication Date |
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EP0575190A2 true EP0575190A2 (en) | 1993-12-22 |
EP0575190A3 EP0575190A3 (en) | 1994-01-26 |
EP0575190B1 EP0575190B1 (en) | 1997-09-17 |
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ID=15669458
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EP93304762A Expired - Lifetime EP0575190B1 (en) | 1992-06-17 | 1993-06-17 | Fe-base soft magnetic alloy and process for making same |
Country Status (5)
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---|---|
EP (1) | EP0575190B1 (en) |
JP (1) | JP3623970B2 (en) |
KR (1) | KR0131376B1 (en) |
CA (1) | CA2098532A1 (en) |
DE (1) | DE69313938T2 (en) |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4444482A1 (en) * | 1994-12-14 | 1996-06-27 | Bosch Gmbh Robert | Soft magnetic material |
CN102360670A (en) * | 2011-10-24 | 2012-02-22 | 南京信息工程大学 | Composite material with ferrite magnetic layer and amorphous soft magnetic core as well as preparation method thereof |
CN111640550A (en) * | 2019-03-01 | 2020-09-08 | 真空融化股份有限公司 | Alloy and method for producing a magnetic core |
WO2022059966A1 (en) * | 2020-09-21 | 2022-03-24 | 엘지전자 주식회사 | Alloy powder and preparation method therefor |
US11349113B2 (en) | 2018-04-10 | 2022-05-31 | Lg Energy Solution, Ltd. | Method of producing iron phosphide, positive electrode for lithium secondary battery comprising iron phosphide, and lithium secondary battery comprising same |
CN117026103A (en) * | 2023-08-08 | 2023-11-10 | 中南大学 | Multi-component soft magnetic alloy with high strength, high resistance and low resistance temperature coefficient, and preparation method and application thereof |
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KR100916602B1 (en) * | 2002-11-11 | 2009-09-11 | 엘지디스플레이 주식회사 | Liquid Crystal Display Using Soda Lime Glass and Manufacturing Method Thereof |
CN104962821B (en) * | 2015-05-26 | 2017-03-22 | 北京科技大学 | Machining method of wire printer yoke iron seat part |
JP7106919B2 (en) * | 2018-03-23 | 2022-07-27 | Tdk株式会社 | Soft magnetic thin films, thin film inductors and magnetic products |
WO2019198949A1 (en) * | 2018-04-10 | 2019-10-17 | 주식회사 엘지화학 | Method of producing iron phosphide, positive electrode for lithium secondary battery comprising iron phosphide, and lithium secondary battery comprising same |
KR102229460B1 (en) * | 2018-04-10 | 2021-03-18 | 주식회사 엘지화학 | Method for manufacturing iron phosphide |
CN112176222B (en) * | 2020-10-30 | 2021-12-17 | 东北大学 | A kind of Fe-Ni permalloy material containing Ce and preparation method thereof |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0316811A2 (en) * | 1987-11-17 | 1989-05-24 | Hitachi Metals, Ltd. | Anti-theft sensor marker |
JPH04272159A (en) * | 1991-01-08 | 1992-09-28 | Sumitomo Metal Ind Ltd | Ferrous magnetic alloy |
-
1992
- 1992-06-17 JP JP15833892A patent/JP3623970B2/en not_active Expired - Lifetime
-
1993
- 1993-06-16 CA CA002098532A patent/CA2098532A1/en not_active Abandoned
- 1993-06-17 EP EP93304762A patent/EP0575190B1/en not_active Expired - Lifetime
- 1993-06-17 KR KR1019930011091A patent/KR0131376B1/en not_active IP Right Cessation
- 1993-06-17 DE DE69313938T patent/DE69313938T2/en not_active Expired - Fee Related
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
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EP0316811A2 (en) * | 1987-11-17 | 1989-05-24 | Hitachi Metals, Ltd. | Anti-theft sensor marker |
JPH04272159A (en) * | 1991-01-08 | 1992-09-28 | Sumitomo Metal Ind Ltd | Ferrous magnetic alloy |
Non-Patent Citations (2)
Title |
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JOURNAL OF APPLIED PHYSICS. vol. 70, no. 10 , 15 November 1991 , NEW YORK US pages 6241 - 6243 Y.FUJII ET AL * |
PATENT ABSTRACTS OF JAPAN vol. 17, no. 67 (C-1025)10 February 1993 & JP-04 272 159 (SUMITOMO METAL IND) * |
Cited By (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4444482A1 (en) * | 1994-12-14 | 1996-06-27 | Bosch Gmbh Robert | Soft magnetic material |
CN102360670A (en) * | 2011-10-24 | 2012-02-22 | 南京信息工程大学 | Composite material with ferrite magnetic layer and amorphous soft magnetic core as well as preparation method thereof |
US11349113B2 (en) | 2018-04-10 | 2022-05-31 | Lg Energy Solution, Ltd. | Method of producing iron phosphide, positive electrode for lithium secondary battery comprising iron phosphide, and lithium secondary battery comprising same |
CN111640550A (en) * | 2019-03-01 | 2020-09-08 | 真空融化股份有限公司 | Alloy and method for producing a magnetic core |
WO2022059966A1 (en) * | 2020-09-21 | 2022-03-24 | 엘지전자 주식회사 | Alloy powder and preparation method therefor |
CN117026103A (en) * | 2023-08-08 | 2023-11-10 | 中南大学 | Multi-component soft magnetic alloy with high strength, high resistance and low resistance temperature coefficient, and preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
EP0575190A3 (en) | 1994-01-26 |
KR940006157A (en) | 1994-03-23 |
DE69313938T2 (en) | 1998-03-05 |
DE69313938D1 (en) | 1997-10-23 |
CA2098532A1 (en) | 1993-12-18 |
EP0575190B1 (en) | 1997-09-17 |
KR0131376B1 (en) | 1998-04-24 |
JP3623970B2 (en) | 2005-02-23 |
JPH062076A (en) | 1994-01-11 |
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