Nd-based two-phase separation amorphous alloy

Abstract

Provided is a Nd-based two-phase separation amorphous alloy by adding an element having a big difference in heat of mixing in a Nd-based alloy with a superior amorphous formability through an inherent characteristic of compositional elements and consideration of thermodynamics, at the time of forming amorphous phase, to thereby enable two-phase separation amorphous alloy during solidification. The Nd-based two-phase separation amorphous alloy which is represented as a general equation Nd100-a-b(TM)a(D)b wherein TM is a transition metal which is a combination of respective one selected from A-B, A-C and B-C when a group of A consists of Y, Ti, Zr, La, Pr, Gd, and Hf, a group of B consists of Fe, and Mn, and a group of C consists of Co, Ni, Cu, and Ag, wherein the content of the element group which constitutes each combination is 5 atomic weight % or greater, and the element selected from each element group is at least one, and wherein D is at least one selected from the group consisting of Al, B, Si and P, and a and b have the range of 20≦a≦80, and 5≦b≦30, respectively, in terms of atomic weight %.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

The above and other objects and advantages of the present invention will become more apparent by describing the preferred embodiment thereof in more detail with reference to the accompanying drawings in which:

FIGS. 1A and 1B are graphical views illustrating differential thermal analysis results and X-ray diffraction analysis results with respect to a two-phase separation amorphous alloy of Nd₂₅Zr₃₅Co₃₀Al₁₀ according to the present invention, respectively;

FIG. 2 is a photographical view illustrating transmission electron microscope analysis results with respect to a two-phase separation amorphous alloy of Nd₂₅Zr₃₅Co₃₀Al₁₀ according to the present invention;

FIG. 3 is a graphical view illustrating differential thermal analysis results with respect to alloys of Nd—Fe—X—Al according to the present invention;

FIG. 4 is a photographical view illustrating transmission electron microscope analysis results with respect to a two-phase separation amorphous alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ after having undergone selective nano-crystallization through a thermal process according to the present invention;

FIG. 5 is a graphical view illustrating height variation measurement results of a specimen according to temperature using a thermo-mechanical analyzer (TMA) with respect to an alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention;

FIG. 6 is a graphical view illustrating results which is obtained by measuring a magnetic field versus magnetization behavior according to temperature using a vibrating sample magnetometer (VSM) with respect to an alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention.

DETAILED DESCRIPTION OF THE INVENTION

A neodymium-based (Nd-based) two-phase separation amorphous alloy according to preferred embodiments of the present invention will be described below with reference to the accompanying drawings.

(Manufacturing of a Specimen)

1. Manufacturing of a Mother Alloy

In order to obtain a mother alloy of a desired alloy composition in the present invention, Nd which has a purity of 99.8%-99.99%, and elements selected from a group of A such as Y, Ti, Zr, La, Pr, Gd, and Hf, a group of B such as Fe and Mn, a group of C such as Co, Ni, Cu, and Ag, and a group of D such as Al, B, Si, and P elements have been arc-melted under a high purity argon gas atmosphere of 99.99%. Moreover, in order to remove any segregation of the alloy component during the arc-melting, a sample has been repeatedly melted three times while inverting.

2. Manufacturing of a Specimen Using a Melt Spinning Method

The prepared mother alloy has been manufactured into a specimen of a ribbon-shape by using a melt spinning method whose cooling rate is 10⁴-10⁶ K/s.

Concretely, the mother alloy has been firstly charged into a quartz tube. Then, the mother alloy has been melted to liquid state under the argon atmosphere of 7-9 KPa with a microwave induction heating after having maintained a degree of vacuum in a chamber into about 10⁻⁴ Torr. Here, the molten metal is being maintained by a surface tension in the quartz tube. Then, the quartz tube has rapidly fallen before the reaction of the quartz tube has occurred after the mother alloy has been completely melted, and simultaneously the argon gas of about 50 KPa has been injected into the quartz tube. Accordingly, the molten metal is melt-spinned on the Cu roll surface (wheel surface velocity: about 40 m/s) which rotates at a high speed, to thereby manufacture a ribbon-shaped specimen of the thickness of about 30 μm and the width of about 2 mm.

3. Manufacturing of a Specimen Using an Injection Casting Method

In the present invention, the mother alloy has been manufactured into a bulk specimen through an injection casting method while changing a cooling speed by using a copper mold of various diameters. The high purity argon gas is charged at the high vacuum state. The mother alloy has been melted with a high frequency induction under the argon atmosphere. Then, the melted mother alloy has been charged a water-cooled copper mold through a certain fixed injection pressure, to thereby manufacture a rod-shaped specimen of a fixed length of 50 mm.

The analysis of the amorphous alloy composition according to the present invention is as follows.

(Specimen Analysis)

1. Transmission Electron Microscope Analysis

The transmission electron microscope (TEM) analysis has been conducted in order to observe the phase separation phenomenon of a bulk amorphous alloy. The specimen manufactured using an injection casting has been mechanically grinded and prepared by ion milling method. An angle between an ion beam and a specimen surface has been polished while changing into 4-8° by using the ion milling method.

Under the same condition as the above-described condition, a bright field image (BF image) and a limit viewing direction selected area diffraction pattern (SADP) has been obtained at the acceleration voltage of 200 kV using JEM 2000EX.

2. Differential Thermal Analysis

In general, in order to estimate thermodynamic properties which relate to a glass transition temperature (Tg) of an amorphous phase, and a crystallization temperature (Tc), a differential scanning calorimetry (Perkin Elmer, DSC7) has been used.

In this experiment, a sample has been put into a copper fan, and then put in a platinum holder. Then, an empty pan has been put into a reference. The thermodynamic properties have been measured under the high purity argon atmosphere of 99.999% at the temperature range of 373-953 K in order to prevent the oxidation of the specimen. The DSC analysis has been performed under the 99.99% purity argon atmosphere after having charged a sample of about 20 mg at a constant temperature-up rate of 40 K/min(0.667 K/s).

3. X-Ray Diffraction Analysis

In order to identify whether the manufactured specimen has an amorphous phase, an X-ray diffractometry (M18XHF²²-SRA, monochromatic Cu K radiation) has been used to irradiate X-rays onto the specimen. The X-ray diffraction analysis has been performed with the condition of a tube voltage of 50 kV and current of 200 mA of a Cu target (λ=1.5406, Ka₁ ray). X-ray diffraction spectrum has been obtained within the range of a scanning range of 20°-80° with a sequential scanning method, at the speed of 4°/min while maintaining 0.02° interval.

In general, in the case of an amorphous specimen, a broad diffraction pattern with no crystalline picks has been obtained in the X-ray diffraction analysis. Differently from the general amorphous alloy, the diffraction patterns regarding the two amorphous phases have been overlapped in the two-phase amorphous alloy. As a result, it can be confirmed that the present invention has a relatively wider diffraction angle region.

4. TMA Analysis

In a supercooled liquid region, TMA (TMA-7, Perkin-Elmer) has been used in order to measure viscosity of the amorphous alloy. By using a specimen of a rod-shape and a ribbon-shape, a certain compressive load is applied by a ceramic probe whose diameter is 3 mm at a compressed mode, and then a change in length of a specimen has been measured while increasing the temperature. Correction for temperature has been performed using In and Zn specimens before all the experiments. The experiment has been progressed under the Ar atmosphere.

5. VSM (Vibrating Sample Magnetometer) Analysis

A macroscopic magnetism change has been measured according to temperature in the form of a ribbon or powder with respect to the two-phase amorphous alloy according to the invention using a VSM (Vibrating Sample Magnetometer). A change in a magnetic property (or magnetization) according to temperature has been measured with a magnetic force of 2 tesla at maximum and at the range of the temperature of 10 K to 300 K.

TABLE 1
(Unit: Kelvin Temp.)
						Manufacturing/
Items	Composition (at %)	Tg1	Tx1	Tg2	Tx2	form
Examples	1	Nd25Zr35Co30Al10	468	488	671	719	M/DA
	2	Nd30Zr25Hf5Co30Al10	477	501	667	712	M/DA
	3	Nd50Ti10Co30Al10	496	519	562	587	M/DA
	4	Nd15Y40Co25Al20	598	646	810	848	M/DA
	5	Nd30La30Co30Al10	462	498	554	586	M/DA
	6	Nd30Ti30Fe30Al10	470	498	705	727	M/DA
	7	Nd30Gd30Fe30Al10	472	508	823	857	M/DA
	8	Nd50Mn20Co15Al15	534	562	682	715	M/DA
	9	Nd50Fe10Co25Al15	528	570	752	782	I/DA
	10	Nd50Fe5Co30Al12B3	527	560	769	789	I/DA
	11	Nd57Fe10Co15Al15Si3	478	507	688	727	M/DA
	12	Nd60Fe10Ni15Al15	471	499	717	762	I/DA
	13	Nd50Fe5Ni30Al12P3	530	561	752	766	M/DA
	14	Nd50Fe20Ag15Al15	492	522	716	784	I/DA
	15	Nd50Fe10Ag20Cu5Al15	499	524	735	758	M/DA
Comparative	1	Nd60Fe30Al10	—	—	712	797	M/SA
Examples	2	Nd70Fe10Co5Al15	—	—	—	734	M/Comp.
	3	Nd10Fe75Co7B8	—	—	—	870	M/Comp.
	4	Nd56Zr4Co30Al10	496	521	—	—	M/SA
	5	Nd30V30Fe30Al10	—	—	732	776	M/Comp.
	6	Nd30Nb30Co30Al10	—	—	—	—	M/Cryst.
	7	Nd60Fe15Mn15Al10	—	—	—	—	M/Cryst.
	8	Nd50Ni20Cu15Al15	503	542	—	—	M/SA
	9	Nd50Fe20Zn15Al15	—	—	—	—	M/Cryst.
	10	Nd65Mn17Co15Si3	—	—	—	—	M/Cryst.
	11	Nd40Mn15Cu10Al35	—	—	—	—	M/Cryst.
	12	Nd25Zr35Co30C10	—	—	—	—	M/Cryst.

Here, M=Melt spinning method, I.=Injection casting method, SA=single amorphous state, DA=two-phase amorphous state, Cryst.=crystallization, and Comp.=SA+Cryst.

As can be seen from Table 1, the alloys according to the present invention have two-phase separation amorphous microstructure (DA) during solidification. The glass forming ability of the two-phase separation amorphous alloy depends on cooling rates greater than that of the single amorphous alloy. However, in the case of the Nd—Fe—Co—Al group, the Nd—Fe—Ni—Al group, and the Nd—Fe—Ag—Al group amorphous alloy according to the present invention, the two-phase amorphous can be obtained through an injection casting method having a relatively small cooling rate of about 10-100 K/S.

In Comparative Example 1, only the element of the B group among the TM is selected. This violates the present invention requirement that at least two groups should be selected among the TM. The immiscible area is not formed due to the absence of the elements which has a positive heat of mixing. Thus, the Comparative Example 1 shows an example in which the amorphous alloy of the simple Nd-based single phase is formed.

In Comparative Example 2, the elements of TM are added by less than 20 wt %. In this case, the TM gets to deviate from a eutectic composition with Nd. Then, the glass forming ability of this alloy is reduced. As a result, a complete amorphous phase is not obtained even through a rapid solidification process.

In Comparative Example 3, the elements of TM are added in excess of 80 wt %. The TM element (Fe) becomes a main component in this composition. Accordingly, the TM gets to deviate from a eutectic composition in a combination of Nd-TM-(D group), to thereby greatly reduce the glass forming ability. As a result, a complete amorphous phase is not obtained even through a rapid solidification process.

In Comparative Example 4, the element of the A group among the TM is added by less than 5 wt % which is presented on the basis of a minimum standard. In this case, an element of the A group, Zr is insufficient in quantity to form an immiscible area together with the main element Nd. Thus, the Comparative Example 4 shows an example in which the amorphous alloy of the Nd-based single phase is formed.

In Comparative Examples 5 and 6, the other elements of V and Nb are added instead of the A group element according to the present invention. In these cases, although they have the positive heat of mixing value of 18 KJ/mole and 32 KJ/mole with respect to Nd, respectively, they have a relatively high melting temperature when the elements of V and Nb are combined with the other compositional elements. Accordingly, the Comparative Examples 5 and 6 violate the empirical formula for amorphous phase formation that they have to have the deep eutectic composition. Thus, the Comparative Examples 5 and 6 show an example that formation of amorphous phase is not facilitated even through a rapid solidification process, respectively.

In Comparative Example 7, only the element of the B group among the TM is selected. This violates the present invention requirement that at least two groups should be selected among the TM. Thus, the Comparative Example 7 shows an example in which two-phase separation of amorphous are not facilitated even through a rapid solidification process.

In Comparative Example 8, only the element of the C group among the TM is selected. This violates the present invention requirement that at least two groups should be selected among the TM. Thus, Comparative Example 8 shows an example that the Nd-based single phase of amorphous is made since it has a difficulty in forming an immiscible area.

In Comparative Example 9, zinc (Zn) which is an element other than those of the present invention is added as an element of TM. The Comparative Example 9 shows an example that amorphous is not achieved even through a rapid solidification since the glass forming ability is very reduced.

In Comparative Examples 10 and 11, the element of the D group is added by less than 5 wt % or in excess of 30 wt %. These show that the element of the D group which has been added by less than 5 wt % or in excess of 30 wt % plays a negative role in a correlation between the existing elements and thus amorphous is not achieved even through a rapid solidification since the glass forming ability is abruptly reduced.

In Comparative Example 12, a semi-metal or non-metal element different from the D group elements is added. Accordingly, when carbon (C) is added, the Comparative Example 12 violates the empirical formula for enhancing glass forming ability glass forming ability in the Nd-based alloy. Thus, the Comparative Example 12 shows an example that amorphous is not obtained even through a rapid solidification process.

Hereinbelow, a Nd-based two-phase separation amorphous alloy according to the present invention will be described in more detail with reference to the accompanying drawings.

FIGS. 1A and 1B are graphical views illustrating differential thermal analysis results and X-ray diffraction analysis results with respect to a two-phase separation amorphous alloy of Nd₂₅Zr₃₅Co₃₀Al₁₀ according to the present invention, respectively. As can be seen from FIG. 1A, the two-phase separation amorphous alloy of the present invention shows a crystallization behavior conspicuously separated by the difference in the crystallization temperature range of main elements with a positive heat of mixing relationship. Moreover, as can be seen from FIG. 1B, the two-phase separation amorphous alloy of the present invention shows a typical amorphous halo pattern in an inherent two-theta (20) section which has been determined by the inherent atom radius of main elements whose two phases have been separated by a positive heat of mixing relationship from an X-ray diffraction analysis result. As a result, a diffraction pattern which two halo patterns have been overlapped can be obtained.

FIG. 2 is a photographical view illustrating transmission electron microscope analysis results with respect to a two-phase separation amorphous alloy of Nd₂₅Zr₃₅Co₃₀Al₁₀ according to the present invention. As can be seen from FIG. 2, in the case of a two-phase separation amorphous alloy of Nd₂₅Zr₃₅Co₃₀Al₁₀ according to the present invention, two halo rings which are separated by the atom radius difference of a respectively separated amorphous main element are obtained similarly to the X-ray diffraction analysis results. The shape of amorphous phases obtained in this two-phase separation alloy of Nd₂₅Zr₃₅Co₃₀Al₁₀ is indistinguishable through a Bright Field Image due to a similar density value of the separated amorphous phase, but definitively distinguishable through a Dark Field Image.

FIG. 3 is a graphical view illustrating differential thermal analysis results with respect to alloys of Nd—Fe—X—Al according to the present invention. As can be seen from FIG. 3, it can be confirmed that a crystallization behavior for each separated ally occurs in two divided temperature ranges by a positive heat of mixing relationship. In this way, the alloy composition having the separated crystallization behavior has a supercooled liquid region of a certain temperature area showing a super plasticity behavior before the crystallization behavior, respectively.

FIG. 4 is a photographical view illustrating transmission electron microscope analysis results of a sample which has undergone a thermal process up to 600 K, with respect to a two-phase separation amorphous alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention. As can be seen from FIG. 4, in the case that the two-phase separation alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention is thermally treated up to 600 K, it can be confirmed that nano-crystalline phase having particle size of several tens of nano-meters have partially appeared by a first crystallization behavior relating to a Nd-based amorphous phase, and an amorphous phase is maintained for the other regions. That is, it can be confirmed that the crystallized region and the amorphous region have a composite form of a nano-scale. As a result, it is possible to perform a selective crystallization due to the separated crystallization behavior of the two-phase separation amorphous alloy, to thereby manufacture nano-composite materials.

FIG. 5 is a graphical view illustrating height variation measurement results of a specimen according to temperature using a thermo-mechanical analyzer (TMA) with respect to an alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention. In the case of the alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention, it can be confirmed that a sudden height variation is undergone in a first supercooled liquid region (450-500 K) which relates to the Nd-based amorphous phase. This is the same result as that of the previously known super plastic deformation of the amorphous alloy. However, in the case of the two-phase separation amorphous alloy composition of the present invention, it can be confirmed that a step portion (a sudden height decreasing area according to the temperature increment) which has implied that a second variation is possible in a supercooled liquid region (680-740 K) relating to a second crystallization behavior relating to Zr differently from a single amorphous phase. In the vicinity of about 900 K (that is, at the solidus melting temperature (Ts), a sudden height reduction is initiated in connection with the melting of the Nd-based amorphous alloy.

FIG. 6 is a graphical view illustrating results which is obtained by measuring a magnetic field versus magnetization behavior according to temperature using a vibrating sample magnetometer (VSM) with respect to an alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention. In the case of the two-phase separation alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention, as shown in FIG. 6, a spin reorientation temperature in which orientation of spins begins to be changed is about 30 K. That is, in the room temperature, the spins are oriented to an out-of-plane direction. If the temperature gets to fall down to 30 K or less, the spins rotate while forming a cone. As a result, an in-plane component of the spins is generated so that a magnetization value increases in an in-plane direction. This phenomenon is one of the general properties which show up in the magnetic materials. However, in the case of the two-phase separation alloy of the present invention, it can be confirmed that the magnetic property drastically changes from the soft magnetic characteristic to the hard magnetic characteristic, at the spin reorientation temperature due to the presence of a second amorphous phase. This phenomenon is taken into consideration that the two-phase separation alloy of Nd₃₀Ti₃₀Co₃₀Al₁₀ according to the present invention can be used as a data storage medium etc., since spins are firstly oriented in an in-plane direction at the low temperature, a preference magnetization direction is changed according to a temperature, and a magnetism switching is possible at the time of applications with a little temperature change.

As described above, a Nd-based alloy which enables two-phase amorphous alloy according to the present invention has the following effects.

1) An amorphous alloy composition can be manufactured in an in-situ manner through a thermodynamic access, in which a two-phase amorphous material having an excellent glass forming ability is phase-separated from the amorphous alloy composition and then phase-separated amorphous material exists.

2) A phase separation mechanism applied in the amorphous alloy composition according to the present invention, presents standards designing an amorphous material in a new concept differing from previously proposed empirical formulas as well as opposing the general empirical formulas regarding the amorphous formation. Furthermore, two-phase bulk amorphous alloy compositions by the phase separation can be easily developed in the other alloy systems in the future.

3) The two-phase separation amorphous alloy according to the present invention exhibits a phase separation having a quite fine connection structure of a nano-scale. Thus, a two-phase separated composition can be selectively nano-crystallized through a selective thermal process or a control of a cooling rate, to thereby easily manufacture an amorphous based nano-composite material.

4) The two-phase separation amorphous alloy according to the present invention shows two supercooled liquid regions in respect of both of the two amorphous phases. Accordingly, a multi-stage deformational behavior is available in the supercooled liquid region. In more detail, a supercooled liquid region using the super-plasticity of the amorphous material for the existing micro electro mechanical systems (MEMS), including, the processing of the material through microforming etc., is mainly used, but the two amorphous phases of the invention have the supercooled liquid region separately with respect to the respective amorphous phase in the case of the alloy according to the present invention. It is possible to obtain an amorphous based composite material through a nano-crystallization process by appearance of the second supercooled liquid region, to accordingly be applicable as a new processing method for a nano-composite material.

5) In the case of the Nd-based two-phase amorphous alloy according to the present invention, a magnetic property is improved by a nano-phase which can be easily formed through the second amorphous phase or a thermal process of the two-phase amorphous alloy. In this way, a neodymium-based amorphous alloy which enables a nano-structure control has a big potential in view of high value-added industry applications including electric and electronic industries etc., differently from the existing concept for enhancing the magnetic property through nano-crystallization relying upon various kinds of thermal treatments and processes.

As described above, the present invention has been described with respect to particularly preferred embodiments. However, the present invention is not limited to the above embodiments, and it is possible for one who has an ordinary skill in the art to make various modifications and variations, without departing off the spirit of the present invention.

Claims

1. A Nd-based two-phase separation amorphous alloy which is represented as a general equation Nd100-a-b(TM)a(D)b wherein TM is a transition metal which is one combination selected from A-B, A-C and B-C when an element group of A consists of Y, Ti, Zr, La, Pr, Gd and Hf, an element group of B consists of Fe and Mn, and an element group of C consists of Co, Ni, Cu and Ag,wherein the content of the element group which constitutes each combination is 5 atomic weight % or greater, and the element selected from each group is at least one, andwherein D is at least one selected from the group consisting of Al, B, Si and P, and a and b have the range of 20≦a≦80, and 5≦b≦30, respectively, in terms of atomic weight %.

2. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Zr—Co—Al alloy.

3. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Hf—Co—Al alloy.

4. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Zr—Hf—Co—Al alloy.

5. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Y—Co—Al alloy.

6. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Ti—Co—Al alloy.

7. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—La—Co—Al alloy.

8. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Pr—Co—Al alloy.

9. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Ti—Fe—Al alloy.

10. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Gd—Fe—Al alloy.

11. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Pr—Fe—Al alloy.

12. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Gd—Pr—Fe—Al alloy.

13. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Fe—Co—Al alloy.

14. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Fe—Co—Al—B alloy.

15. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Fe—Co—Al—Si alloy.

16. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Fe—Ni—Al alloy.

17. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Fe—Co—Ni—Al alloy.

18. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Fe—Cu—Al alloy.

19. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Fe—Ag—Al alloy.

20. The Nd-based two-phase separation amorphous alloy according to claim 1, wherein the amorphous alloy is a Nd—Fe—Ag—Cu—Al alloy.