WO2015190528A1 - Fe基ナノ結晶合金コア、及びFe基ナノ結晶合金コアの製造方法 - Google Patents

Fe基ナノ結晶合金コア、及びFe基ナノ結晶合金コアの製造方法 Download PDF

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WO2015190528A1
WO2015190528A1 PCT/JP2015/066758 JP2015066758W WO2015190528A1 WO 2015190528 A1 WO2015190528 A1 WO 2015190528A1 JP 2015066758 W JP2015066758 W JP 2015066758W WO 2015190528 A1 WO2015190528 A1 WO 2015190528A1
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core
magnetic field
temperature
frequency
khz
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French (fr)
Japanese (ja)
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森次 仲男
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日立金属株式会社
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Application filed by 日立金属株式会社 filed Critical 日立金属株式会社
Priority to EP20160649.8A priority Critical patent/EP3693980A1/de
Priority to ES15807434T priority patent/ES2791885T3/es
Priority to CN201580019461.6A priority patent/CN106170837B/zh
Priority to JP2016527844A priority patent/JP6137408B2/ja
Priority to EP15807434.4A priority patent/EP3157021B1/de
Publication of WO2015190528A1 publication Critical patent/WO2015190528A1/ja

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    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F1/00Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties
    • H01F1/01Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials
    • H01F1/03Magnets or magnetic bodies characterised by the magnetic materials therefor; Selection of materials for their magnetic properties of inorganic materials characterised by their coercivity
    • H01F1/12Magnets 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
    • H01F1/14Magnets 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
    • H01F1/147Alloys characterised by their composition
    • H01F1/153Amorphous metallic alloys, e.g. glassy metals
    • H01F1/15333Amorphous metallic alloys, e.g. glassy metals containing nanocrystallites, e.g. obtained by annealing
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C33/00Making ferrous alloys
    • C22C33/08Making cast-iron alloys
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/002Ferrous alloys, e.g. steel alloys containing In, Mg, or other elements not provided for in one single group C22C38/001 - C22C38/60
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/02Ferrous alloys, e.g. steel alloys containing silicon
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/12Ferrous alloys, e.g. steel alloys containing tungsten, tantalum, molybdenum, vanadium, or niobium
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C38/00Ferrous alloys, e.g. steel alloys
    • C22C38/16Ferrous alloys, e.g. steel alloys containing copper
    • 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
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F3/00Cores, Yokes, or armatures
    • H01F3/04Cores, Yokes, or armatures made from strips or ribbons
    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01FMAGNETS; INDUCTANCES; TRANSFORMERS; SELECTION OF MATERIALS FOR THEIR MAGNETIC PROPERTIES
    • H01F41/00Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties
    • H01F41/02Apparatus or processes specially adapted for manufacturing or assembling magnets, inductances or transformers; Apparatus or processes specially adapted for manufacturing materials characterised by their magnetic properties for manufacturing cores, coils, or magnets
    • H01F41/0206Manufacturing of magnetic cores by mechanical means
    • H01F41/0213Manufacturing of magnetic circuits made from strip(s) or ribbon(s)
    • H01F41/0226Manufacturing of magnetic circuits made from strip(s) or ribbon(s) from amorphous ribbons
    • CCHEMISTRY; METALLURGY
    • C22METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
    • C22CALLOYS
    • C22C2202/00Physical properties
    • C22C2202/02Magnetic

Definitions

  • the present invention relates to an Fe-based nanocrystalline alloy core wound with an Fe-based nanocrystalline alloy and a method for producing an Fe-based nanocrystalline alloy core.
  • Fe-based nanocrystalline alloys have excellent soft magnetic properties that can achieve both a high saturation magnetic flux density Bs and a high relative permeability ⁇ r, and are therefore used in cores such as common mode choke coils and high frequency transformers.
  • Fe—Cu—M′—Si—B Fe—Cu—M′—Si—B (M ′ is a group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo described in Patent Document 1).
  • M ′ is a group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo described in Patent Document 1).
  • the composition of the (at least one element selected) system is representative.
  • the Fe-based nanocrystalline alloy is obtained by microcrystalline (nanocrystallizing) an amorphous alloy obtained by rapidly solidifying a liquid phase alloy heated to a temperature equal to or higher than the melting point by heat treatment.
  • a method for rapid solidification from the liquid phase for example, a single roll method excellent in productivity is adopted.
  • the alloy obtained by rapid solidification takes the form of a ribbon or ribbon.
  • the Fe-based nanocrystalline alloy has different magnetic characteristics such as relative permeability ⁇ and squareness ratio by applying a temperature profile during heat treatment and applying a magnetic field in a specific direction during heat treatment.
  • Patent Document 2 in order to obtain an Fe-based nanocrystalline alloy having an initial relative permeability ⁇ i of 70,000 or more and a squareness ratio of 30% or less, a magnetic field is applied in the width direction of the alloy ribbon (core height direction). It has been proposed to heat-treat while applying. As specific examples of the heat treatment in Patent Document 2, various profiles have been proposed. Generally, the heat treatment is held while applying a magnetic field in the highest temperature range of the heat treatment. There are those that hold while applying a magnetic field over the cooling process and those that hold while applying the magnetic field from the highest temperature range to the cooling process.
  • Patent Document 2 The heat treatment method disclosed in Patent Document 2 is considered effective as a means for reducing the squareness ratio.
  • impedance relative permeability ⁇ rz As a characteristic index as a common mode choke, impedance relative permeability ⁇ rz is often used.
  • the impedance relative permeability ⁇ rz is described in, for example, JIS standard C2531 (revised in 1999).
  • the impedance relative permeability ⁇ rz can be considered as being equal to the absolute value of the complex relative permeability ( ⁇ r′ ⁇ i ⁇ r ′′) as shown in the following equation (for example, “Point of Magnetic Material Selection”, 1989). Issued on November 10, 2011, edited by Keizo Ota).
  • ⁇ rz ( ⁇ r ′ 2 + ⁇ r ′′ 2 ) 1/2
  • the real part ⁇ r ′ of the complex relative permeability in the above formula represents a magnetic flux density component with no phase delay with respect to the magnetic field, and generally corresponds to the magnitude of the impedance relative permeability ⁇ rz in the low frequency range.
  • the imaginary part ⁇ r ′′ represents a magnetic flux density component including a phase lag with respect to the magnetic field and corresponds to a loss of magnetic energy. In a high frequency range (for example, 50 kHz or more), the noise suppression effect becomes higher as the imaginary part ⁇ r ′′ is higher.
  • the impedance relative permeability ⁇ rz expressed by the above formula is used as an index for evaluating the noise suppression effect for a wide frequency band. If the impedance relative permeability ⁇ rz is a high value in a wide frequency band, it is excellent in the ability to absorb and remove common mode noise.
  • the present inventor has studied to make the impedance relative permeability ⁇ rz higher in a wide band of frequencies from 10 kHz to 1 MHz. As a result, it has been recognized that it is difficult to obtain a high impedance relative permeability ⁇ rz in a wide frequency band with the heat treatment profiles described in Patent Document 1 and Patent Document 2.
  • the present invention has been made in view of the above, and an Fe-based nanocrystalline alloy core having a high impedance relative permeability ⁇ rz in a wide frequency band from 10 kHz to 1 MHz, and a method for producing the Fe-based nanocrystalline alloy core.
  • the purpose is to provide.
  • the frequency is 10 kHz to 1 MHz by applying a magnetic field only within a specific temperature range during the temperature rising period.
  • the present inventors have found that an Fe-based nanocrystalline alloy core having a high impedance relative permeability ⁇ rz can be obtained in a wide band of the present invention.
  • the core according to the embodiment of the present invention includes a heat treatment step in which a nano-crystallizable Fe-based amorphous alloy ribbon is wound and then heated to a crystallization temperature region and cooled.
  • a core produced through The impedance relative permeability ⁇ rz of the core is More than 90,000 at a frequency of 10 kHz 40,000 or more at a frequency of 100 kHz, and More than 8,500 at 1MHz frequency It is.
  • the impedance relative permeability ⁇ rz of the core is 105,000 or more at a frequency of 10 kHz, 45,000 or more at a frequency of 100 kHz, and More than 9,000 at 1MHz frequency It is preferable that
  • the Fe-based nanocrystalline alloy ribbon preferably has a thickness of 9 ⁇ m or more and 20 ⁇ m or less.
  • a method for producing a core comprises heating a nano-crystallizable Fe-based amorphous alloy ribbon and then heating to a crystallization temperature region, A heat treatment step of cooling, wherein the heat treatment step is within a temperature range during a temperature rise period corresponding to a temperature from a high crystallization start temperature of 25 ° C. to a high temperature of 60 ° C. of the crystallization start temperature in a differential scanning calorimeter. Limiting, it has a magnetic field application process which applies a magnetic field to the height direction of the core in 10 minutes or more and 60 minutes or less.
  • the heat treatment step is performed within a temperature range during the temperature increase period from a high crystallization start temperature of 30 ° C. to a high crystallization start temperature of 50 ° C. in a differential scanning calorimeter. It is preferable to include a magnetic field applying step of applying a magnetic field in the height direction of the core in 15 to 40 minutes.
  • a magnetic field having a magnetic field strength of 50 kA / m or more and 300 kA / m or less is applied in the height direction of the core in the magnetic field application step.
  • an Fe-based nanocrystalline alloy ribbon having a thickness of 9 ⁇ m or more and 20 ⁇ m or less.
  • a method for producing an Fe-based nanocrystalline alloy ribbon includes a step of preparing an Fe-based amorphous alloy ribbon capable of nanocrystallization, and winding the Fe-based amorphous alloy ribbon. Including a step of forming a wound body, a heat treatment step of heating and cooling the wound body to a crystallization temperature region, and a step of applying a magnetic field to the wound body during the heat treatment step.
  • the step of applying the magnetic field is at least one in a temperature range from a high crystallization start temperature of 25 ° C. to a high crystallization start temperature of 60 ° C. indicated by the differential scanning calorimeter during the temperature rising period of the heat treatment step.
  • a magnetic field of a predetermined strength (for example, 50 kA / m) or more is applied along the height direction of the wound body (the width direction of the alloy ribbon) during the period of the portion, and a part of the temperature rise period A magnetic field greater than or equal to the predetermined intensity in a period Not applied to the wound body. More specifically, the magnetic field is applied within a time range of 10 minutes or more and 60 minutes or less, limited to a temperature range from 25 ° C. as the crystallization start temperature to 60 ° C. as the crystallization start temperature. The magnetic field is not applied in a temperature range other than the above temperature range during the temperature rising period.
  • a predetermined strength for example, 50 kA / m
  • a magnetic field having a predetermined strength or higher is not applied during a temperature rising period equal to or lower than the crystallization start temperature or when reaching the maximum temperature of the heat treatment step (a temperature higher than 60 ° C. than the crystallization start temperature).
  • an Fe-based nanocrystalline alloy core having a high impedance relative permeability ⁇ rz can be obtained in a wide frequency band from 10 kHz to 1 MHz.
  • the Fe-based nanocrystalline alloy core can be manufactured. For this reason, it is optimal for a common mode choke or the like in which characteristics in a wide frequency band from 10 kHz to 1 MHz are important.
  • FIG. 3 is a diagram showing a measurement result of a Fe-based amorphous alloy ribbon described in Example 1 using a differential scanning calorimeter (DSC). It is a graph which shows that the frequency characteristic of impedance relative permeability (micro
  • a magnetic field when a magnetic field is applied in the width direction of the wound ribbon (the height direction as the core) to obtain the Fe-based nanocrystalline alloy, it is limited to a specific temperature range of the temperature rising period.
  • a heat treatment step is performed while applying a magnetic field.
  • the temperature is limited to a temperature range during a temperature rising period from a high crystallization start temperature of 25 ° C. to a high crystallization start temperature of 60 ° C. in the differential scanning calorimeter. Then, a magnetic field application step is performed in which a magnetic field is applied in the height direction of the core for a time of 10 minutes to 60 minutes.
  • the magnetic field is applied only during a specific period of the temperature rising period, and when the maximum temperature of the heat treatment is reached or during the period of the cooling process after reaching the maximum temperature. Does not apply a magnetic field.
  • the maximum temperature of the heat treatment is typically higher than the temperature of 60 ° C. higher than the crystallization start temperature.
  • the “temperature increase period” means a period before the maximum temperature is reached, and before reaching the maximum temperature, the temperature is increased, decreased, and maintained at a constant temperature.
  • the state may be included.
  • the heat treatment is held for a certain time at a specific temperature within the temperature range. May be done to do.
  • the temperature may be monotonously increased at a constant temperature increase rate, or the temperature increase rate may be changed in the middle.
  • FIG. 6 is a graph showing the frequency characteristic of the impedance relative permeability obtained by the experiment of the present inventor, and the frequency of the impedance relative permeability of the core (core C1) when no magnetic field is applied during the heat treatment. The characteristics and the frequency characteristics of the impedance relative permeability of the core (core C2) when a magnetic field is applied throughout the heat treatment period are shown.
  • the impedance relative permeability ⁇ rz of the core C1 greatly exceeds the impedance permeability ⁇ rz of the core C2 (always magnetic field applied).
  • the impedance permeability ⁇ rz of the core C2 is higher than the impedance permeability ⁇ rz of the core C1.
  • the impedance relative permeability ⁇ rz in the low frequency region (according to the experiments by the present inventor, in particular, the real part ⁇ r of the complex relative permeability) It was confirmed that the impedance ratio permeability ⁇ rz in the high frequency range tends to be improved.
  • the present inventor has recognized that the improvement in the impedance relative permeability ⁇ rz on the low frequency side and the improvement in the impedance relative permeability ⁇ rz on the high frequency side are contradictory.
  • the present inventors repeated various experiments on heat treatment in a magnetic field, we confirmed the existence of conditions with little decrease in impedance relative permeability on the low frequency side in heat treatment at low temperature for a short time, and conducted further diligent studies. I did it.
  • the heat treatment step it is limited to a temperature range during the temperature rising period corresponding to from the high crystallization start temperature of 25 ° C. in the differential scanning calorimeter to the high crystallization start temperature of 60 ° C. Improving the impedance relative permeability ⁇ rz in the high frequency range while suppressing the decrease in the impedance relative permeability ⁇ rz in the low frequency range by applying a magnetic field in the height direction of the core for a time of 60 minutes or less. I found out that I can.
  • ⁇ rz at a frequency of 10 kHz is 90,000 to 115,000 and ⁇ rz at a frequency of 100 kHz.
  • 40,000 to 49,000 and a ⁇ rz of 8,500 to 15,000 at a frequency of 1 MHz can be obtained.
  • the impedance relative permeability ⁇ rz can be maximized in a wide frequency band from a frequency of 10 kHz to 1 MHz by applying a magnetic field limited within a certain temperature range of the temperature raising period.
  • the mechanism of how the magnetic field application limited to a certain temperature range of the temperature rising period contributes to each of ⁇ ′ and ⁇ ′′ has not been elucidated.
  • the above crystallization start temperature is determined by a differential scanning calorimeter. It is difficult to accurately measure the true crystallization start temperature, and identification by a differential scanning calorimeter (DSC) is effective.
  • the temperature at which an exothermic reaction due to the start of nanocrystallization was detected during the temperature rise was defined as the crystallization start temperature (see FIG. 5).
  • the crystallization start temperature means a value obtained when the measurement conditions of the differential scanning calorimeter are performed at a heating rate of 10 ° C./min.
  • the heat treatment temperature is controlled so that the temperature distribution in the actual heat treatment furnace becomes plus or minus 5 ° C. or less, taking into consideration the capacity of the heat treatment furnace and the amount of heat generated by crystallization of the amorphous alloy ribbon to be heat treated. It is preferable to control. Thereby, the magnetic properties of the alloy after heat treatment can be stabilized.
  • the strength of the applied magnetic field is preferably 50 kA / m or more and 300 kA / m or less. If the applied magnetic field is too weak, it is difficult to impart induced magnetic anisotropy under actual working conditions. If it is too high, induced magnetic anisotropy tends to be imparted too much. A more preferable range is 60 kA / m or more and 280 kA / m.
  • the magnetic field to be applied is a relatively weak magnetic field of less than 50 kA / m
  • An elongated amorphous alloy ribbon can be obtained by melting an alloy having the above composition to a melting point or higher and rapidly solidifying it by a single roll method.
  • the thickness of the amorphous alloy ribbon is preferably 9 ⁇ m or more and 30 ⁇ m or less. If it is less than 9 ⁇ m, the mechanical strength of the ribbon is insufficient, and it is easy to break during handling. When it exceeds 30 ⁇ m, it is difficult to stably obtain an amorphous state. In addition, when the amorphous alloy ribbon is nanocrystallized and used as a core for high frequency applications, an eddy current is generated in the ribbon, and the loss due to the eddy current increases as the ribbon becomes thicker. Therefore, a more preferable thickness is 9 ⁇ m to 20 ⁇ m, and a thickness of 15 ⁇ m or less is further preferable.
  • the width of the amorphous alloy ribbon is preferably 10 mm or more from the practical shape of the core. Since a cost can be reduced by slitting (cutting) a wide alloy ribbon, a wide width is preferable, but a width of 250 mm or less is preferable for stable production of the alloy ribbon. In order to manufacture more stably, 70 mm width or less is more preferable.
  • the heat treatment for nanocrystallization is preferably performed in an inert gas such as nitrogen, and the maximum temperature reached is preferably more than 560 ° C. and 600 ° C. or less.
  • the temperature is 560 ° C. or lower or exceeds 600 ° C., magnetostriction increases, which is not preferable.
  • the holding time at the highest temperature is not specifically set and is 0 minute (no holding time), nanocrystallization can be performed. In consideration of the heat capacity of the total amount of the alloy to be heat-treated and the stability of the characteristics, it can be held for 3 hours or less.
  • the temperature profile of the heat treatment is, for example, compared with a temperature increase rate of 3 to 5 ° C./min from room temperature to near the temperature at which nanocrystallization starts (typically 20 ° C. lower than the crystallization start temperature).
  • the temperature is rapidly increased, and thereafter, from the vicinity of the above-mentioned nanocrystallization start temperature to 60 ° C higher than the start temperature of nanocrystallization (or to the highest temperature reached), the average is 0.2 to 1.0 ° C / min.
  • Stable nanocrystallization can be performed by increasing the temperature at a moderate temperature increase rate. Note that it is preferable to cool at a cooling rate of 2 to 5 ° C./min from the highest temperature to 200 ° C.
  • the alloy can be taken out into the atmosphere at 100 ° C. or lower.
  • a heat treatment step may be performed in which a nano-crystallizable Fe-based amorphous alloy ribbon is wound to produce an annular body, and then heated to a crystallization temperature region and cooled.
  • a predetermined induced magnetic anisotropy can be imparted.
  • This Fe-based amorphous alloy ribbon was slit (cut) to a width of 15 mm, and then wound around an outer diameter of 31 mm and an inner diameter of 21 mm to produce a toroidal core (height 15 mm).
  • the crystallization start temperature of this alloy was 500 ° C. as measured by a differential scanning calorimeter (DSC).
  • the produced core was subjected to heat treatment and magnetic field application with the temperature and magnetic field application profiles shown in FIG.
  • the magnetic field is applied for 30 minutes in a temperature range of 530 to 550 ° C. (a temperature range from a high crystallization start temperature of 30 ° C. to a high crystallization start temperature of 50 ° C.).
  • the magnetic field application direction was the width direction of the alloy ribbon, that is, the height direction of the core.
  • the magnetic field strength was 280 kA / m.
  • the maximum temperature reached in the heat treatment is 580 ° C.
  • the impedance relative permeability ⁇ rz was measured using HP4194A manufactured by Agilent Technologies under the conditions of an oscillation level of 0.5 V and an average of 16.
  • the insulation coated conductor was passed through the center of the toroidal core and connected to an input / output terminal for measurement.
  • Example 1 the impedance relative permeability ⁇ rz was 98,000 at 10 kHz, 42,000 at 100 kHz, and 8,600 at 1 MHz.
  • Example 2 Using the Fe-based amorphous alloy described in Example 1, a toroidal core was similarly produced. The prepared core was subjected to heat treatment and magnetic field application with the temperature and magnetic field application profiles shown in FIG. Only the temperature range of magnetic field application and the magnetic field strength are different from those of the first embodiment (FIG. 1), and other conditions are the same as those of the first embodiment.
  • the magnetic field is applied for 15 minutes in a temperature range of 540 to 550 ° C. (temperature range from 40 ° C. as the crystallization start temperature to 50 ° C. as the crystallization start temperature).
  • the magnetic field strength was 160 kA / m.
  • Table 1 shows the measurement results of impedance relative permeability ⁇ rz at 10 kHz, 100 kHz, and 1 MHz of the core after the heat treatment.
  • Example 2 the impedance relative permeability ⁇ rz was 109,000 at 10 kHz, 47,000 at 100 kHz, and 9,500 at 1 MHz. That is, a higher impedance relative permeability ⁇ rz could be obtained at each frequency of 10 kHz, 100 kHz, and 1 MHz compared to Example 1.
  • Example 3 A single-roll method using a molten alloy (at the same as in Example 1) consisting of atomic percent, Cu: 1%, Nb: 3%, Si: 15.5%, B: 6.5%, remaining Fe and inevitable impurities To obtain an Fe-based amorphous alloy ribbon having a width of 50 mm and a thickness of 10 ⁇ m. A toroidal core was similarly produced using this Fe-based amorphous alloy ribbon having a thickness of 10 ⁇ m (13 ⁇ m in Example 1). In the same manner as in Example 2, the prepared core was subjected to heat treatment and magnetic field application with the temperature and magnetic field application profiles shown in FIG. Table 1 shows the measurement results of impedance relative permeability ⁇ rz at 10 kHz, 100 kHz, and 1 MHz of the core after the heat treatment.
  • Example 3 the impedance relative permeability ⁇ rz was 91,000 at 10 kHz, 46,000 at 100 kHz, and 9,300 at 1 MHz.
  • Example 4 Using the Fe-based amorphous alloy ribbon having a thickness of 13 ⁇ m described in Example 1, a toroidal core was similarly produced. A magnetic field was applied to the prepared core at an intensity of 160 kA / m for 15 minutes at a heat treatment temperature in the range of 530 ° C. to 540 ° C. Table 1 shows the measurement results of impedance relative permeability ⁇ rz at 10 kHz, 100 kHz, and 1 MHz of the core after the heat treatment.
  • Example 4 the impedance permeability ⁇ rz was 90,000 at 10 kHz, 46,000 at 100 kHz, and 10,000 at 1 MHz.
  • Comparative Example 1 Using the Fe-based amorphous alloy described in Example 1, a toroidal core was similarly produced. The manufactured core was heat-treated with the temperature and magnetic field application profile shown in FIG. 3 without applying a magnetic field (no magnetic field). As can be seen from FIG. 3, the temperature profile in Comparative Example 1 is the same as in Example 1.
  • Table 1 shows the measurement results of impedance relative permeability ⁇ rz at 10 kHz, 100 kHz, and 1 MHz of the core after the heat treatment.
  • Comparative Example 2 Using the Fe-based amorphous alloy described in Example 1, a toroidal core was similarly produced. The prepared core was subjected to heat treatment and magnetic field application with the temperature and magnetic field application profiles shown in FIG. As can be seen from FIG. 4, the temperature profile in Comparative Example 2 is the same as in Example 1.
  • Example 2 the magnetic field strength in the magnetic field application is the same as in Example 1 (FIG. 1), but the temperature range of the magnetic field application reaches the cooling after reaching the highest equivalent temperature of 580 ° C. from the start of the heat treatment. is there.
  • the temperature range of this magnetic field application is outside the scope of the present invention.
  • Table 1 shows the measurement results of impedance relative permeability ⁇ rz at 10 kHz, 100 kHz, and 1 MHz of the core after the heat treatment.
  • the application of the magnetic field was continuously performed for about 60 minutes over a temperature range of 480 to 520 ° C. (temperature range from 20 ° C. lower than the crystallization start temperature to 20 ° C. higher than the crystallization start temperature).
  • the magnetic field application direction was the width direction of the alloy ribbon, that is, the core height direction, and the magnetic field strength was 120 kA / m.
  • Table 1 shows the measurement results of impedance relative permeability ⁇ rz at 10 kHz, 100 kHz, and 1 MHz of the core after the heat treatment.
  • FIG. 6 shows frequency characteristics of impedance relative permeability ⁇ rz in the core (core E1) according to the embodiment of the present invention (similar to Example 2) and the core (core R1) according to the above reference example.
  • FIG. 6 also shows the core (core C1) when no magnetic field is applied corresponding to Comparative Example 1, and the core (core C2) when the magnetic field corresponding to Comparative Example 2 is continuously applied. Yes.
  • the magnetic field is applied for a relatively short time at the crystallization start temperature of 25 ° C. or higher and 60 ° C. or lower (typically, the magnetic field is not applied when the maximum temperature is reached) as in the embodiment of the present invention (core E1). It was confirmed that the impedance relative permeability ⁇ rz was improved not only in the high frequency range but also in the low frequency range. As described above, in the embodiment of the present invention, a unique effect of improving the impedance relative permeability ⁇ rz in the low frequency region is obtained even in the form in which the magnetic field is applied in the specific period before the maximum temperature.
  • a core exhibiting a high impedance relative permeability ⁇ rz corresponding to a wide frequency band is provided, and is suitably used in a common mode choke coil, a high frequency transformer, or the like.

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PCT/JP2015/066758 2014-06-10 2015-06-10 Fe基ナノ結晶合金コア、及びFe基ナノ結晶合金コアの製造方法 WO2015190528A1 (ja)

Priority Applications (5)

Application Number Priority Date Filing Date Title
EP20160649.8A EP3693980A1 (de) 2014-06-10 2015-06-10 Magnetkern aus fe-basierter nanokristalliner legierung
ES15807434T ES2791885T3 (es) 2014-06-10 2015-06-10 Método para producir núcleo de aleación nanocristalina basada en Fe
CN201580019461.6A CN106170837B (zh) 2014-06-10 2015-06-10 Fe基纳米晶合金磁芯和Fe基纳米晶合金磁芯的制造方法
JP2016527844A JP6137408B2 (ja) 2014-06-10 2015-06-10 Fe基ナノ結晶合金コア、及びFe基ナノ結晶合金コアの製造方法
EP15807434.4A EP3157021B1 (de) 2014-06-10 2015-06-10 Verfahren zur herstellung eines fe-basierten nanokristallinen legierungskerns

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Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2018062310A1 (ja) * 2016-09-29 2019-06-24 日立金属株式会社 ナノ結晶合金磁心、磁心ユニットおよびナノ結晶合金磁心の製造方法
WO2020162480A1 (ja) * 2019-02-05 2020-08-13 日立金属株式会社 巻磁心、合金コアおよび巻磁心の製造方法
CN112410531A (zh) * 2020-11-12 2021-02-26 中国科学院宁波材料技术与工程研究所 一种纳米晶合金及其制备方法

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20180171444A1 (en) * 2016-12-15 2018-06-21 Samsung Electro-Mechanics Co., Ltd. Fe-based nanocrystalline alloy and electronic component using the same
CN109754974B (zh) * 2019-03-07 2021-06-01 中国科学院宁波材料技术与工程研究所 一种纳米晶合金磁芯及其制备方法
CN111151745B (zh) * 2019-12-28 2021-06-04 同济大学 一种铁基材料的改性方法

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS596360A (ja) * 1982-07-02 1984-01-13 Sony Corp 非晶質磁性合金の熱処理方法
JPH0296306A (ja) * 1988-06-10 1990-04-09 Nippon Telegr & Teleph Corp <Ntt> 非晶質磁性薄帯巻鉄心
JPH05267031A (ja) * 1992-02-14 1993-10-15 Takeshi Masumoto 磁心材料
JP2000328206A (ja) * 1999-03-12 2000-11-28 Hitachi Metals Ltd 軟磁性合金薄帯ならびにそれを用いた磁心、装置およびその製造方法
JP2001316724A (ja) * 2000-05-10 2001-11-16 Alps Electric Co Ltd 高周波用磁心の製造方法
WO2015046140A1 (ja) * 2013-09-27 2015-04-02 日立金属株式会社 Fe基ナノ結晶合金の製造方法及びFe基ナノ結晶合金磁心の製造方法

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR0134508B1 (ko) * 1990-03-27 1998-04-27 아오이 죠이치 자심
JPH044393A (ja) 1990-04-20 1992-01-08 Hitachi Ltd 配管の制振要素,制振要素を備えた配管及び制振要素を備えた圧力伝達機器
JP2909349B2 (ja) * 1993-05-21 1999-06-23 日立金属株式会社 絶縁膜が形成されたナノ結晶軟磁性合金薄帯および磁心ならびにパルス発生装置、レーザ装置、加速器
JP3719449B2 (ja) 1994-04-15 2005-11-24 日立金属株式会社 ナノ結晶合金およびその製造方法ならびにそれを用いた磁心
JPH0917623A (ja) * 1995-06-30 1997-01-17 Hitachi Metals Ltd ナノ結晶合金磁心およびその製造方法
KR102007522B1 (ko) * 2008-08-22 2019-08-05 가부시키가이샤 토호쿠 마그네토 인스티튜트 합금 조성물, Fe계 나노 결정 합금 및 그 제조 방법, 및 자성 부품

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS596360A (ja) * 1982-07-02 1984-01-13 Sony Corp 非晶質磁性合金の熱処理方法
JPH0296306A (ja) * 1988-06-10 1990-04-09 Nippon Telegr & Teleph Corp <Ntt> 非晶質磁性薄帯巻鉄心
JPH05267031A (ja) * 1992-02-14 1993-10-15 Takeshi Masumoto 磁心材料
JP2000328206A (ja) * 1999-03-12 2000-11-28 Hitachi Metals Ltd 軟磁性合金薄帯ならびにそれを用いた磁心、装置およびその製造方法
JP2001316724A (ja) * 2000-05-10 2001-11-16 Alps Electric Co Ltd 高周波用磁心の製造方法
WO2015046140A1 (ja) * 2013-09-27 2015-04-02 日立金属株式会社 Fe基ナノ結晶合金の製造方法及びFe基ナノ結晶合金磁心の製造方法

Cited By (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPWO2018062310A1 (ja) * 2016-09-29 2019-06-24 日立金属株式会社 ナノ結晶合金磁心、磁心ユニットおよびナノ結晶合金磁心の製造方法
JP2019201215A (ja) * 2016-09-29 2019-11-21 日立金属株式会社 ナノ結晶合金磁心の製造方法
JP2021002663A (ja) * 2016-09-29 2021-01-07 日立金属株式会社 ナノ結晶合金磁心の製造方法
JP7028290B2 (ja) 2016-09-29 2022-03-02 日立金属株式会社 ナノ結晶合金磁心の製造方法
WO2020162480A1 (ja) * 2019-02-05 2020-08-13 日立金属株式会社 巻磁心、合金コアおよび巻磁心の製造方法
JPWO2020162480A1 (ja) * 2019-02-05 2021-12-02 日立金属株式会社 巻磁心、合金コアおよび巻磁心の製造方法
JP7143903B2 (ja) 2019-02-05 2022-09-29 日立金属株式会社 巻磁心、合金コアおよび巻磁心の製造方法
US11749430B2 (en) 2019-02-05 2023-09-05 Proterial, Ltd. Wound magnetic core, alloy core, and method for manufacturing wound magnetic core
CN112410531A (zh) * 2020-11-12 2021-02-26 中国科学院宁波材料技术与工程研究所 一种纳米晶合金及其制备方法
CN112410531B (zh) * 2020-11-12 2022-03-08 中国科学院宁波材料技术与工程研究所 一种纳米晶合金及其制备方法

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