CA1323219C - Fe-base soft magnetic alloy and method of producing same - Google Patents
Fe-base soft magnetic alloy and method of producing sameInfo
- Publication number
- CA1323219C CA1323219C CA000553434A CA553434A CA1323219C CA 1323219 C CA1323219 C CA 1323219C CA 000553434 A CA000553434 A CA 000553434A CA 553434 A CA553434 A CA 553434A CA 1323219 C CA1323219 C CA 1323219C
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- alloy
- soft magnetic
- alpha
- base soft
- magnetic alloy
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- C—CHEMISTRY; METALLURGY
- C22—METALLURGY; FERROUS OR NON-FERROUS ALLOYS; TREATMENT OF ALLOYS OR NON-FERROUS METALS
- C22C—ALLOYS
- C22C38/00—Ferrous alloys, e.g. steel alloys
- C22C38/18—Ferrous alloys, e.g. steel alloys containing chromium
- C22C38/40—Ferrous alloys, e.g. steel alloys containing chromium with nickel
- C22C38/54—Ferrous alloys, e.g. steel alloys containing chromium with nickel with boron
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C21—METALLURGY OF IRON
- C21D—MODIFYING THE PHYSICAL STRUCTURE OF FERROUS METALS; GENERAL DEVICES FOR HEAT TREATMENT OF FERROUS OR NON-FERROUS METALS OR ALLOYS; MAKING METAL MALLEABLE, e.g. BY DECARBURISATION OR TEMPERING
- C21D1/00—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering
- C21D1/04—General methods or devices for heat treatment, e.g. annealing, hardening, quenching or tempering with simultaneous application of supersonic waves, magnetic or electric fields
-
- 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
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- Engineering & Computer Science (AREA)
- Organic Chemistry (AREA)
- Materials Engineering (AREA)
- Mechanical Engineering (AREA)
- Metallurgy (AREA)
- Physics & Mathematics (AREA)
- Dispersion Chemistry (AREA)
- Electromagnetism (AREA)
- Power Engineering (AREA)
- Thermal Sciences (AREA)
- Crystallography & Structural Chemistry (AREA)
- Soft Magnetic Materials (AREA)
Abstract
ABSTRACT OF THE DISCLOSURE
An Fe-base soft magnetic alloy having the composition represented by the general formula:
(Fe1-aMa)100-x-y-z-.alpha.-.beta.-.gamma.CuxSiyBzM'.alpha.M".beta.X.gamma.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, M"
is at least one element selected from the group consisting of V, Cr, Mn, A?, elements in the platinum group, Sc, Y, rare earth elements, Au, Zn, Sn and Re, X is at least one element selected from the group consisting of C, Ge, P, Ga, Sb, In, Be and As, and a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30, 0.1?.alpha.?30, .beta.?10 and .gamma.?10, at least 50% of the alloy structure being fine crystalline particles having an average particle size of 1000.ANG.
or less. This alloy has low core loss, time variation of core loss, high permeability and low magnetostriction.
An Fe-base soft magnetic alloy having the composition represented by the general formula:
(Fe1-aMa)100-x-y-z-.alpha.-.beta.-.gamma.CuxSiyBzM'.alpha.M".beta.X.gamma.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, M"
is at least one element selected from the group consisting of V, Cr, Mn, A?, elements in the platinum group, Sc, Y, rare earth elements, Au, Zn, Sn and Re, X is at least one element selected from the group consisting of C, Ge, P, Ga, Sb, In, Be and As, and a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30, 0.1?.alpha.?30, .beta.?10 and .gamma.?10, at least 50% of the alloy structure being fine crystalline particles having an average particle size of 1000.ANG.
or less. This alloy has low core loss, time variation of core loss, high permeability and low magnetostriction.
Description
~3~32~L~
BACKGROUND OF THE INVENTION
The present invention xelates to an Fe-base soft magnetic alloy having excellent magnetic properties, and more particularly to an Fe-base soft magnetic alloy having a low magnetostriction suitable for various transformers, choke coils, saturable reactors, magnetic heads, etc. and metnods of producing them.
Conventionally used as magnetic materials for high-frequenc~ transformers, magnetic heads, saturable reactors, choke coils, etc. are mainly ferrites having such advantages as low eddy current loss. However, since ferrites have a low saturation magnetic flux density and poor temperature characteristics, it is difEicult to miniaturize magnetic cores made of ferrites for high-frequency transformers, choke coils etc.
Thus, in these applications, alloys having particularly small magnetostriction are desired because they have relatively good soft magnetic properties even when internal strain remains after impregnation, molding or working, which tend to deteriorate magnetic properties thereof. As soft magnetic alloys having small magnetostriction, 6.5-weight %
~ilicone steel, ~e-Si-AQ alloy, 80-weight % Ni Permalloy, etc.
are known, which have saturation magnetostriction ~s of nearly O .
~3~3219 However, although the silicone steel has a high saturation magnetic flux density, it is poor in soft magnetic properties, particularly in permeability and core loss at high frequency. Although Fe-Si-AQ alloy has better soft magnetic properties than the silicone steel, it is still insufficient as compared with Co-base amorphous alloys, and further since it is brittle, its thin ribbon is extremely difficult to wind or work. 80-weight % Ni Permalloy has a low saturation magnetic flux density of about 8KG and a small magnetostriction, but it is easily subjected to plastic deformation which serves to deteriorate its characteristics.
Recently, as an alternative to such conventional magnetic materials, amorphous magnetic alloys having a high saturation magnetic flux density have been atracting much attention, and those having various compositions have been developed. Amorphous alloys are mainly classified into two categories: iron-base alloys and cobalt-base alloys. Fe-base amorphous alloys are advantageous in that they are less expensive than Co-base amorphous alloys, but they generally have larger core loss and lower permeability at high frequency than the Co-base amorphous alloys. On the other hand, despite the fact that the Co-base amorphous alloys have small core loss and high permeability at high frequency, their core loss and permeability vary largerly as the time passes, posing problems in practical use. Further, since they contain as a main component an expensive cobalt, they are inevitably disadvantageous in terms of cost.
Under such circumstances, various proposals have been :~ . :
,, .
.
i ~
~3~321~
made on Fe-base soft magnetic alloys.
Japanese Patent Publication No. 60-17019 discloses an ixon-base, boron-containing magnetic amorphous alloy having the composition of 74-84 atomic % of Fe, 8-24 atomic % of B and at least one of 16 atomic % or less of Si and 3 atomic ~ or less of C, at least 85% of its structure being in the form of an amorphous metal matrix, crystalline alloy particle precipitates being discontinuously distributed in the overall amorphous metal matrix, the crystalline perticles having an average particle size of 0.05-l~m and an average particle-to-particle distance of l-10~m, and the particles occupying 0.01-0.3 of the total volume. It is reported that the crystalline particles in this alloy are ~-tFe, Si) particles discontinuously distributed and acting as pinning sites of magnetic domain walls. However, despite the fact that this Fe-base amorphous magnetic alloy has a low core loss because of the presence of discontinuous crystalline particles, the core loss i~; still large for intended purposes, and its permeability does not reach the level of Co-base amorphous alloys, so that it is not satisfactory as magnetic core material for high-frequency transformers and chokes intended in the present invention.
Japanese Patent Laid-Open No. 60-52557 discloses a low-core loss, amorphous magnetic alloy having the formula FeaCubBcSid, wherein 75<a<~5, 0<b<1.5, 10<c<20, d~l0 and c+d<30. However, although this Fe-base amorphous alloy has an extremely reduced core loss because of Cu, it is still unsatisfactory li~e the above Fe-base amorphous alloy containing crystalline particles. Further, it is not -.~ , ... .- -'. ' ' .; ' ;`.: ,. ' ': ' : ` :
::
1,~23219 satisfactory in terms of the time variability of core loss permeability, etc.
Further, an attempt has been made to reduce magnetostriction and also core loss by adding Mo or Nb (Inomata et al., J. Appl. Phys. 54(11), Nov. 1983, pp.6553-6557).
However, it is known that in the case of an Fe-base amorphous alloy, a saturation magnetostriction ~s is almost in proportion to the square of a saturation magnetization Ms (Makino, et al., Japan Applied Magnetism Association, The 4th Convention material (1978), 43), which means that the magnetostriction cannot be made close to zero without reducing the saturation magnetization to almost zero. Alloys having such composition have extremely low Curie temperatures, unable to be used for practical purposes. Thus, Fe-base amorphous alloys presently used do not have sufficiently low magnetostriction, so that when impregnated with resins, they have deteriorated soft matnetic characteristics which are extremely inferior to those of Co~base amorphous alloys.
BACKGROUND OF THE INVENTION
The present invention xelates to an Fe-base soft magnetic alloy having excellent magnetic properties, and more particularly to an Fe-base soft magnetic alloy having a low magnetostriction suitable for various transformers, choke coils, saturable reactors, magnetic heads, etc. and metnods of producing them.
Conventionally used as magnetic materials for high-frequenc~ transformers, magnetic heads, saturable reactors, choke coils, etc. are mainly ferrites having such advantages as low eddy current loss. However, since ferrites have a low saturation magnetic flux density and poor temperature characteristics, it is difEicult to miniaturize magnetic cores made of ferrites for high-frequency transformers, choke coils etc.
Thus, in these applications, alloys having particularly small magnetostriction are desired because they have relatively good soft magnetic properties even when internal strain remains after impregnation, molding or working, which tend to deteriorate magnetic properties thereof. As soft magnetic alloys having small magnetostriction, 6.5-weight %
~ilicone steel, ~e-Si-AQ alloy, 80-weight % Ni Permalloy, etc.
are known, which have saturation magnetostriction ~s of nearly O .
~3~3219 However, although the silicone steel has a high saturation magnetic flux density, it is poor in soft magnetic properties, particularly in permeability and core loss at high frequency. Although Fe-Si-AQ alloy has better soft magnetic properties than the silicone steel, it is still insufficient as compared with Co-base amorphous alloys, and further since it is brittle, its thin ribbon is extremely difficult to wind or work. 80-weight % Ni Permalloy has a low saturation magnetic flux density of about 8KG and a small magnetostriction, but it is easily subjected to plastic deformation which serves to deteriorate its characteristics.
Recently, as an alternative to such conventional magnetic materials, amorphous magnetic alloys having a high saturation magnetic flux density have been atracting much attention, and those having various compositions have been developed. Amorphous alloys are mainly classified into two categories: iron-base alloys and cobalt-base alloys. Fe-base amorphous alloys are advantageous in that they are less expensive than Co-base amorphous alloys, but they generally have larger core loss and lower permeability at high frequency than the Co-base amorphous alloys. On the other hand, despite the fact that the Co-base amorphous alloys have small core loss and high permeability at high frequency, their core loss and permeability vary largerly as the time passes, posing problems in practical use. Further, since they contain as a main component an expensive cobalt, they are inevitably disadvantageous in terms of cost.
Under such circumstances, various proposals have been :~ . :
,, .
.
i ~
~3~321~
made on Fe-base soft magnetic alloys.
Japanese Patent Publication No. 60-17019 discloses an ixon-base, boron-containing magnetic amorphous alloy having the composition of 74-84 atomic % of Fe, 8-24 atomic % of B and at least one of 16 atomic % or less of Si and 3 atomic ~ or less of C, at least 85% of its structure being in the form of an amorphous metal matrix, crystalline alloy particle precipitates being discontinuously distributed in the overall amorphous metal matrix, the crystalline perticles having an average particle size of 0.05-l~m and an average particle-to-particle distance of l-10~m, and the particles occupying 0.01-0.3 of the total volume. It is reported that the crystalline particles in this alloy are ~-tFe, Si) particles discontinuously distributed and acting as pinning sites of magnetic domain walls. However, despite the fact that this Fe-base amorphous magnetic alloy has a low core loss because of the presence of discontinuous crystalline particles, the core loss i~; still large for intended purposes, and its permeability does not reach the level of Co-base amorphous alloys, so that it is not satisfactory as magnetic core material for high-frequency transformers and chokes intended in the present invention.
Japanese Patent Laid-Open No. 60-52557 discloses a low-core loss, amorphous magnetic alloy having the formula FeaCubBcSid, wherein 75<a<~5, 0<b<1.5, 10<c<20, d~l0 and c+d<30. However, although this Fe-base amorphous alloy has an extremely reduced core loss because of Cu, it is still unsatisfactory li~e the above Fe-base amorphous alloy containing crystalline particles. Further, it is not -.~ , ... .- -'. ' ' .; ' ;`.: ,. ' ': ' : ` :
::
1,~23219 satisfactory in terms of the time variability of core loss permeability, etc.
Further, an attempt has been made to reduce magnetostriction and also core loss by adding Mo or Nb (Inomata et al., J. Appl. Phys. 54(11), Nov. 1983, pp.6553-6557).
However, it is known that in the case of an Fe-base amorphous alloy, a saturation magnetostriction ~s is almost in proportion to the square of a saturation magnetization Ms (Makino, et al., Japan Applied Magnetism Association, The 4th Convention material (1978), 43), which means that the magnetostriction cannot be made close to zero without reducing the saturation magnetization to almost zero. Alloys having such composition have extremely low Curie temperatures, unable to be used for practical purposes. Thus, Fe-base amorphous alloys presently used do not have sufficiently low magnetostriction, so that when impregnated with resins, they have deteriorated soft matnetic characteristics which are extremely inferior to those of Co~base amorphous alloys.
2 0 OBJECT AND SUMMARY OF THÆ INVENTION
Therefore, an object of the present invention is to provide an Fe-base soft magnetic alloy having excellent magnetic characteristics such as core loss, time variability of core loss, permeability, etc.
Another object of the present invention is to provide an Fe-base soft magnetic alloy having excellent soft magnetic properties, particularly high-frequency magnetic properties, and also a low magnetostriction which keeps it from suffering ,, ~
, , , ,; : . ~, ~''''' ' ' :, :~ .
' ' ; ` :' ' ':, :: ' ~32~219 from magnetic deterioration by impregnation and deformation.
A further object of the present invention is to provide a method of producing such Fe-base soft magnetic alloys.
Intense research in view of the above objects has revealed that the addition of Cu and at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo to an Fe-base alloy having an essential composition of Fe-Si-B, and a proper heat treatment of the Fe-base alloy which is once made amorphous can provide an Fe-base soft magnetic alloy, a major part of which structure is composed of fine crystalline particles, and thus having excellent soft magnetic properties. It has also been found that by limiting the alloy composition properly, the alloy can have a low magnetostriction. The present invention is based on these findings.
Thus, the Fe-base soft magnetic alloy according to the present invention has the composition represented by the general formula:
(Fe M ) Cu Si B M' l-a a lO0-x-y-z-~ x y z wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, ~If, Ti and Mo, and a, x, y, 2 and ~ respectively satisfy O<a<0.5~ O.l<x<3, O<y<30, O<z<25, 5<y+z<30 and 0.1<~<30, at least 50% of the alloy structure being occupied by fine crystalline particles.
Another Fe-base soft magnetic alloy according to the present invention has the composition represented by the general formula:
"
..
::: ,, :::, 1~3219 ( l-a a)loo-x-y-z-~-~-ycuxsiyBzMl M~3X
wherein is M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, M~ is at least one element selected from the group consisting of V, Cr, Mn, A~, elements in the platinum group, Sc, Y, rare earth elements, Au, Zn, Sn and Re, X is at least one element selected from the group consisting of C, Ge, P, Ga, Sb, In, Be and As, and a, x, y, z, ~, ~ and y respectively satisfy 0<a<0.5, 0.1<x<3, 0<y<30, 0<z<25, 5<y+z<30, 0.1<~<30 ~<10 and y<l0, at least 50% of the alloy structure being fine crystalline particles having an average particle size of lo00A
or less.
Further, the method of producing an Fe-base soft magnetic alloy according to the present invention comprises the steps of rapidly quenching a melt of the above composition and heat treating it to generate fine crystalline particles.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 (a) is a transmission electron photomicroscope (magnification: 300,000) of the Fe-base soft magnetic alloy after heat treatment in Example l;
Fig. 1 (b) is a schematic view of the photomicrograph of Fig. 1 (a);
Fig. 1 (c) is a transmission electron photomicrograph (magnification: 300,000) of the Fe-base soft magnetic alloy of Fe74 5Nb3Sil3 5Bg containing no Cu after heat treatment;
Fig. 1 (d) is a schematic view of the photomicrograph of Fig. 1 (c);
. .
-~ ~ . . , : .
~.
-132321~
Flg. 2 ls a transmission electron photomicrograph (magniflcatlon: 300,000) of the Fe-base soft magnetic alloy of Example 1 before heat treatment;
Fig. 3 (a) is a graph showlng an X-ray dlffraction pattern of the Fe-base soft magnetlc alloy of Example 1 before heat treatment;
Fig. 3 (b) ls a graph showing an X-ray diffraction pattern of the Fe-base soft magnetic alloy of the present inven-tion after heat treatment;
Flg. 4 (see the sheet of Flg. 2) is a graph showing the relatlons between Cu content (x) and core loss W2/10ok wlth re-spect to the Fe-base soft magnetlc alloy of Example g;
Flg. 5 ls a graph showlng the relatlons between M' con-tent (a) and core loss W2\10ok wlth respect to the Fe-base soft magnetlc alloy of Example 12;
Flg. 6 ls a graph showing the relatlons between M' con-tent la) and core loss W2~100k wlth respect to the Fe-base soft magnetic alloy of Example 137 Fig. 7 ls a graph showlng the relatlons between Nb con tent (a) and core loss W2/10ok wlth respect to the Fe-base soft magnetic alloy of Example 14r Flg. 8 ls a graph showlng the relations between frequen-cy and effectlve permeablllty with respect to the Fe-base soft magnetlc alloy of Example 15, the Co-base amorphous alloy and ferrlte; `;
Flg. 9 ls a graph showlng the relatlons between frequen-cy and effectlve permeabllity wlth respect to the Fe-base soft magnetic alloy of Example 16, Co-base amorphous alloy and ferrlte;
- . ,.. . .- ..
. . : , , ~
.,,, :,. , , - .. . .: ...
~323219 Fig. 10 is a graph showing the relations between frequency and ef~ective permeabllity with respect to the Fe-base soft maynet~c alloy of Example 17, Co-base amorphous alloy, Fe-base amorphous alloy and ferrlte;
Fig. 11 (see the sheet of Fig. 7) ls a graph showlng the relations between heat treatment temperature and core 1QSS with respect to the Fe-base soft magnetlc alloy of Example 20;
Fig. 12 is a graph showing the relatlons between heat treatment temperature and core loss with respect to the Fe-base soft magnetlc alloy of Example 21;
Fig. 13 is a graph showlng the relatlons between heat treatment temperature and effective permeablllty of the Fe-base soft magnetic alloy of Example 22;
Fig. 14 is a graph showing the relations between effec-tive permeability ~elk and heat treatment temperature with respect to the Fe-base soft magnetic alloy of E~xample 23;
Fig. 15 is a graph showing the relations betwe~n effec-t:lve permeability and hea-t treatment temperature with respect to the Fe-base soft magnetlc alloy of Example 24;
Fig. 16 (see the sheet of Fig. 13) ls a graph showing the relations between Cu content (x) and Nb content (a) and crystallization temperature with respect to the Fe-base soft magnetic alloy of Example 25;
Flg. 17 ls a graph showing wear after 100 hours of the Fe-base soft magnetic alloy of Example 26;
Fig. 18 is a graph showing the relatlons between Vickers hardness and heat treatment temperature with respect to the Fe-base soft magnetic alloy of ~xample 27;
'. ' ' ,~ ' ' ~ .
' ' ~ 323~
Fig. 19 is a graph showing the dependency of saturation magnetostriction (~s) and saturation magnetic flux density (Bs) on y with respect to the alloy of 73.5 1 3 y 22.5-y of Example 33;
Fig. 20 is a graph showing the saturation magnetostriction (~s) of the (Fe-Cul-Nb3~-Si-B pseudo-ternary alloy;
Fig. 21 is a graph showing the coercive force (Hc) of the (Fe-Cul-Nb3)-Si-B pseudo-ternary alloy;
Fig. 22 is a graph showing the effective permeability ~elk at lkHz of the (Fe-Cul-Nb3)-Si-B pseudo-ternary alloy;
Fig. 23 is a graph showing saturation magnetic flux density (Bs) of the (Fe-Cul-Nb3)-Si-B pseudo-ternary alloy;
Fig. 24 is a graph showing the core loss W2/1ook at lOOkHz and 2kG of the (Fe-Cul-Nb3)-Si-B pseudo-ternary alloy;
Fig. 25 is a graph showing the dependency oE magnetic properties on heat treatment with respect to the alloy of Example 35;
Fig. 26 is a graph showing the dependency of core loss on Bm in Example 37;
Fig. 27 is a graph showing the relations between core loss and frequency with respecat to the Fe-base soft magnetic alloy of the present invention, the conventional Fe-base amorphous alloy, the Co~base amorphous alloy and the ferrite in Example 38;
Figs. 28 ~a)-(d) are respectively graphs showing the direct current B-H curves of the alloys of the present invention in Example 39;
,... . .
'' :
, ~3232~9 Fig. 29 is a graph showing the X-ray diffraction pattern of the Fe-base soft magnetic alloy of Example 40;
Figs. 30 (a)-(c) are views each showing the direct current B-H curve of the Fe-base soft magnetic alloy of the present invention in Example 41;
Fig. 31 is a graph showing the relations between core loss and frequency with respect to the Fe-base soft magnetic alloy of the present invention and the conventional Co-base amorphous alloy in Example 41;
Fig. 32 is à graph showing the relations between magnetization and temperature with respect to the Fe-base soft magnetic alloy of Example 42; and Fig. 33 is a graph showing the heat treatment pattern of the Fe-base soft magnetic alloy of the present invention in Example 43.
DET~ILED DESCRIPTION OF THE INVENTION
In the Fe-base soft magnetic alloy of the present invention, Fe may be substituted by Co and/or Ni in the range of 0-0.5. However, to have good magnetic properties such as low core loss and magnetostriction, the content of Co and/or Ni which is represented by "a" is preferably 0-0.1. Particularly to provide a low-magnetostriction alloy, the range of ~a" is preferably 0-0.05.
In the present invention, Cu is an indispensable element, and its content "x" is 0.1-3 atomic %. When it is less than 0.1 atomic %, substantially no effect on the reduction of core loss and Oll the increase in permeability can J : :
~L323219 be obtained by the addition of Cu. On the other hand, when it exceeds 3 atomic %, the alloy's core loss becomes larger than those containing no Cu, reducing the permeability, too. The preferred content of Cu in the present invention is ~.5-2 atomic %, in which range the core loss is particularly small and the permeability is high.
The reasons why the core loss decreases and the permeability increases by the addition of Cu are not fully clear, but it may be presumed as follows:
Cu and Fe hàve a positive interaction parameter so that their solubility is low. However, since iron atoms or copper atoms tend to gather to form clusters, thereby producing compositional fluctuation. This produces a lot of domains likely to be crystallized to provide nuclei for generating Eine crystalline particles. These crystalline particles are based on Fe, and since Cu is substantially not soluble in Fe, Cu is ejected from the fine crystalline particles, whereby the Cu content in the vicinity of the crystal].ine particles becomes high. This presumably suppresses the growth oE crystalline particles.
Because of the formation of a large number of nuclei and the suppression of the growth of crystalline particles by the addition of Cu, the crystalline particles are made fine, and this phenomenon is accelerated by the inclusion of Nb, Ta, W, Mo, Zr, Hf, Ti, etc.
Without Nb, Ta, W, Mo, Zr, Hf, Ti, etc., the crystalline particles are not fully made fine and thus the soft magnetic properties of the resulting alloy are poor.
:. i`: ~ ' , :, ~ ,, ; , . ; ! , ', ~
: ~ ~ '`:
~3232~9 Particularly Nb and Mo are eEfective, and particularly Nb acts to keep the crystalline particles fine, thereby providing excellent soft magnetic properties. And since a fine crystalline phase based on Fe is formed, the Fe-base soft magnetic alloy of the present invention has smaller magnetostriction than Fe-base amorphous alloys, which means that the Fe-base soft magnetic alloy of the present invention has smaller magnetic anisotropy due to internal stress-strain, resulting in improved soft magnetic properties.
Without the addition of Cu, the crystalline particles are unlikely to be made fine. Instead, a compound phase is likely to be formed and crystallized, thereby deteriorating the magnetic properties.
Si and B are elements particular].y for making fine the alloy structure. The Fe-base soft magnetic alloy of -the present invention is desirably produced by once forming an amorphous alloy with the addition of Si and B, and then forming fine crystalline particles by heat treatment.
The content of Si ("y") and that of B ("z~) are O<y<30 atomic %, O<z<25 atomic %, and 5<y+z<30 atomic %, because the alloy would have an extremely reduced saturation magnetic flux density if otherwise.
In the present invention, the preferred range of y is 6-25 atomic %, and the preferred range of z is 2-25 atomic %, and the preferred range of y~z is 14-30 atomic %. When y exceeds 25 atomic %, the resulting alloy has a relatively large magnetostriction under the condition of good soft magnetic properties, and when y is less than 6 atomic %, sufficient soft .
, . . . -,~
,:
:: . .
:. :
~23219 magnetic properties are not necessarily obtained. The reasons for limiting the content of B ("z~) is that when z is less than 2 atomic %, uniform crystalline particle structure cannot easily be obtained, somewhat deteriorating the soft ma~netic properties, and when z exceeds 25 atomic %, the resulting alloy would have a relatively large magnetostriction under the heat treatment condition of providing good soft magnetic properties.
With respect to the total amount of Si+B (y+z), when y+z is less than 14 atomic %, it is often difficult to make the alloy amorphous, providing relatively poor magnetic properties, and when y+z exceeds 30 atomic % an extreme decrease in a saturation magnetic flux density and the deterioration of soft magnetic properties and the increase in magnetostriction ensue.
More preferably, the contents of Si and B are lO<y<25, 3<z<18 and 18<y+z<28, and this range provides the alloy with excellent soft magnetic properties, particularly a saturation ~agnetostriction in the range of -5xlO 6 _ +5xlO 6.
Particularly preferred range is ll<y<24, 3<z<9 and 18<y+z<27, and this range provides the alloy with a saturation magnetostriction in the range of -1.5xlO 6 _ +1.5xlO 6.
In the present inventionS M' acts when added together with Cu to make the precipitated crystalline particles fine.
M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo. These elements have a function of elevating the crystallization temperature of the alloy, and synergistically with Cu having a function of forming clusters and thus lowering the crystallization temperature, it suppresses the growth of the precipitated crystalline - . ,, .
.:
.
: :
~3~32~
particles, thereby making them fine.
The content Oc M' (~) is 0.1-30 atomic %. When it is less than 0.1 atomic %, sufficient effect of making crystalline particles fine cannot be obtained, and when it exceeds 30 atomic % an extreme decrease in saturation magnetic flux density ensues. The preferred content of M' is 0.1-10 atomic %, and more preferably ~ is 2-8 atomic %, in which range paxtieularly exeellent soft magnetie properties are obtained.
Ineidentally, most preferable as M' is Nb and/or Mo, and partieularly Nb in terms of magnetie properties. The addition of M' provides the Fe-base soft magnetie alloy with as high permeability as that of the Co-base, high-permeability materials.
M", which is at least one element seleeted from the group eonsisting of V, Cr, Mn, AQ, elements in the platinum group, Se, Y, rare earth elements, Au, Zn, Sn and Re, may be added for the purposes of improving eor.rosion resistanee or magnetie properties and of adjusting magnetostrietion, but its content is at most 10 atomie %. When the eontent of M~ exceeds 10 atomie %, an extremely deerease in a saturation magnetie flux density ensues. A particularly preferred amount of M~ is 5 atomie % or less.
Among them, at least one element selected from the group eonsisting of Ru, Rh, Pd, Os, Ir, Pt, Au, Cr and V is eapable of providing the alloy with particularly excellent eorrosion resistanee and wear resistanee, thereby making it suitable for magnetie heads, etc.
The alloy of the present invention may contain 10 atomic % or less of at least one element X selected from the group consisting of C, Ge, P, Ga, Sb, In, Be, As. These elements are effective for making amorphous, and when added with Si and s, they help make the alloy amorphous and also are effective for adjusting the magnetostriction and Curie temperature of the alloy.
In sum, in the Fe-base soft magnetic alloy having the general formula:
l-a a)loo-x-y-æ-~cuxsiyB M~ , the general ranges of`a, x, y, z and a are O<a~0.5 O.l<x<3 O<y<30 O<z<25 5<y+z<30 0.1<~<30, and the preferred ranges thereof are O<a<0.1 O.l<x<3 6<y<25 2<z<25 14<y+z<30 O . 1<~<10, and the more preferable ranges are O<a<0.1 0.5<x<2 lO<y<25 3<z<18 , . ..
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~3232~9 l~<y~z<28 2<a<8, and the most preferable ranges are O~a<0.05 0.5<x<2 ll<y<24 3<z<9 18<y+z<27 2<a<8.
And in the Fe-base soft magnetic alloy having the general formula:
l-a a)loo_x_y_z_a_~_yCUxSiyB M' M7~X , the general ranges of a, x, y, z, a, ~ and y are O<a<0.5 O.l<x<3 O<y<30 O<z<25 5<y+z<30 O.l<a<30 ~<10 y<10, and the preferred ranges are O<a<0.1 O.l<x<3 6<y<25 2<z<25 14<y+z<30 O.l<a<10 . ~ -- ..
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~323219 ~5 y<5, and the more preferable ranges are O~a<0.1 0.5<x<2 lO<y< 5 3<z<18 18<y+z<28 2<~<8 ~<5 y<5~
and the most preEerable ranges are O<a<0.05 0 5<x<2 ll<y<24 3<z<9 18<y+z<27 2<a<8 .
~<5 ~_ The Fe-base soft magnetic alloy having the above composition according to the pr~sent invention has an alloy structure, at least 50% of which consists of fine crystalline particles. These crystalline particles are based on a-Fe having a bcc structure, in which Si and B, etc. are dissolved.
These crystalline particles have an extremely small average particle siæe of looOA or less, and are uniformly distributed in the alloy structure. Incidentally, the average paticle size :,:
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~32~2~9 of the crystalline particles is determined by measuring the maximum size of each particle and averaging them. When the average particle size exceeds loOOA, good soft magnetic properties are not obtained. It is preferably 500~ or less, more preferably 200~ or less and particularly 50-200A. The remaining portion of the alloy structure other than the fine crystalline particles is mainly amorphous. Even with fine crystalline particles occupying substantially 100% of the alloy structure, theFe-base soft magnetic alloy of the present invention has sufficiently good magnetic properties.
Incidentally, with respect to inevitable impurities such as N, O, S, etc., it is to be noted that the inclusion thereof in such amounts as not to deteriorate the desired properties is not regarded as changing the alloy composition of the present invention suitable for magnetic cores, etc.
Next, the method of producing the Fe-base soft magnetic alloy of the present invention will be explained in detail below.
First, a melt of the above composition is rapidly quenched by known liquid quenching methods such as a single roll method, a double roll method, etc. to ~orm amorphous alloy ribbons. Usually amorphous alloy ribbons produced by the single roll method, etc. have a thickness of 5-lOO~m or so, and those having a thickness of 25~m or less are particularly suitable as magnetic core materials for use at high frequency.
These amorphous alloys may contain crystal phases, but the alloy structure is preferably amorphous to make sure the formation of uniform fine crystalline particles by a . :
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subsequent heat treatment. Incidentally, the alloy of the present invention can be produced directly by the liquid quenching method without resorting to heat treatment, as long as proper conditions are selected.
The amorphous ribbons are wound, punched, etched or subjected to any other working to desired shapes before heat treatment, for the reasons -that the ribbons have good workability in an amorphous state, but that once crystallized they lose workability.
The heat treatment is carried out by heating the amorphous alloy ribbon worked to have the desired shape in vaccum or in an inert gas atmosphere such as hydrogen, nitrogen, argon, etc. The temperature and time of the heat `
treatment varies depending upon the composition of the amorphous alloy ribbon and the shape and size of a magnetic core made from the amorphous alloy ribbon, etc., but in general it is preferably 450-700C for 5 minutes to 24 hours. When the heat treatment temperature is lower than 450C, crystallization is unlikely to take place with ease, requiring too much time for the heat treatment. On the other hand, when it exceeds 700C, coarse crystalline particles tend to be formed, making it difficult to obtain fine crystalline particles. And with respect to the heat treatment time, when it is shorter than 5 minutes, it is difficult to heat the overall worked alloy at uniorm temperature, providing uneven magnetic properties, and when it is longer than 24 hours, productivity becomes too low and also the crystalline particles grow excessively, resulting in the deterioration of magnetic properties. The preferred ,. , .:
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:
~3232~ 9 heat treatment conditions are, taking into consideration practicality and uniform temperature control, etc., 500-650C
for 5 minutes to 6 hours.
The heat treatment atmosphere is preferably an inert gas atmosphere, but it may be an oxidizing atmosphere such as the air. Cooling may be carried out properly in the air or in a furnace. And the heat treatment may be conducted by a plurality of steps.
The heat treatment can be carried out in a magnetic field to provide the alloy with magnetic anisotropy. When a magnetic field is applied in parallel to the magnetic path o~ a magnetic core made of the alloy of the present invention in the heat treatment step, the resulting heat-treated magnetic core has a good squareness in a 3-H curve thereof, so that it is particularly suitable for saturable reactors, magnetic switches, pulse compression cores, reactors for preventing spike voltage, etc. On the other hand, when the heat treatment is conducted while applying a magnetic field in perpendicular to the magnetic path of a magnetic core, the B-H curve inclines, providing it with a small squareness ratio and a constant permeability. Thus, it has a wider operational range and thus is suitable for transformers, noise filters, choke coils, etc.
The magnetic field need not be applied always during the heat treatment, and it is necessary only when the alloy is at a temperature lower than the Curie temperature Tc thereof.
In the present inven-tion, the alloy has an elevated Curie temperature because of crystallization than the amorphous . .. : .; :
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~32~219 counterpart, and so the heat treatment in a magnetic field can be carried out at temperatures higher than the Curie temperature of the corresponding amorphous alloy. In a case of the heat treatment in a magnetic field, it may be carried out by two or more steps. Also, a rotational magnetic field can be applied during the heat treatment.
Incidentally, the Fe-base soft magnetic alloy of the present invention can be produced by other methods than liquid quenching methods, such as vapor deposition, ion plating, sputtering, etc. which are suitable for producing thin-film magnetic heads, etc. Further, a rotation liq~id spinning method and a glass-coated spinning method may also be utilized toproduce thin wires.
In addition, powdery products can be produced by a cavitation method, an atomization method or by pulveri2ing thin ribbons prepared by a single roll method, etc.
Such powdery alloys of the present invention can be compressed to produce dust cores or bul]~y products.
When the alloy of the present invention is used for magnetic cores, the surface of the alloy is preperably coated with an oxidation layer by proper heat treatment or chemical treatment, or coated with an insulating layer to provide insulation between the adjacent layers so that the magnetic cores may have good properties.
The present invention will be explained in detail by the following Examples, without intention of restricting the ;-scope of the present invention.
Example 1 , , -:, ' , ' ' , ,: .~: ~' ;
1~232~9 A melt having the composition ~by atomic %) of 1%
Cu, 13.4% Si, 9.1% B, 3.1% Nb and balance substantially Fe was formed into a ribbon of 5mm in width and 18~m in thickness by a single roll method. The X-ray diffraction of this ribbon showed a halo pattern peculiar to an amorphous alloy. A
transmission electron photomicrograph (magnification: 300,000) of this ribbon is shown in Fig. 2. As is clear from the X-ray diffraction and Fig. 2, the resulting ribbon was almost completely amorphous.
Next, this àmorphous ribbon was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter, and then heat-treated in a nitrogen gas atmosphere at 550C for one hour. Fig. l(a) shows a transmission electron photomicrograph (magnification: 300,000) of the heat-treated ribbon. Fig. l(b) schematically shows the fine crystalline particles in the photomicrograph of Fig. l(a). It is evident from Figs. 1 (a) and (b) that most. of the alloy structure of the ribbon after the heat treatment consists of fine crystalline particles. It was also confirmed by X-ray diffraction that the alloy after the heat treatment had crystalline particles. The crystalline particles had an average particle size of about loOA. For comparison, Fig. l(c) shows a transmission electron photomicrograph (magnification:
300,000) of an amorphous alloy of Fe74 5Nb3Sil3 5Bg containing no Cu which was heat-treated at 550C for 1 hour, and Fig. l(d) schematically shows i-ts crystalline particles.
The alloy of the present invention containing both Cu and Nb contains crystalline particles almost in a spherical ; , :
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~32S-3219 shape having an average particle size of about looA. On the other hand, in alloys containing only Nb without Cu, the crystalline particles are coarse and most of them are not in the spherical shape. It was confirmed that the addition of both Cu and Nb greatly affects the size and shape of the resulting crystalline particles.
Next, the Fe-base soft magnetic alloy ribbons before and after the heat treatment were measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2k5 and a frequency of 100kMz. As a result, the core loss was 4000mW/cc before the heat treatment, while it was 220m~/cc after the heat treatment. Effective permeability ~e was also measured at a frequency of lkHz and Hm of 5mOe. As a result, the former (before the heat treatment) was 500, while the latter (after the heat treatment) was 100200. This clearly shows that the heat trea-tment according to the present invention serves to form fine crystalline particles uniformly in the amorphous alloy structure, thereby extremely lowering core loss and enhancing permeability.
Example 2 A melt having the composition (by atomic %) of 1% Cu, 15% Si, 9% B, 3% Nb, 1% Cr and balance substantially Fe was formed into a ribbon of 5mm in width and 18~1m in thickness by a single roll method. The X-ray diffraction of this ribbon showed a halo pattern peculiar to an amorphous alloy as is shown in Fig. 3(a). As is clear from a transmission electron photomicrograph (magnification: 300,000) of this ribbon and the X~ray diffraction shown in Fig~ 3(a), the resulting ribbon ,. -- . .. , ~ : .
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was almost completely amorphous.
Next, this amorphous ribbon was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter, and then heat-treated in the same manner as in Example 1. Fig. 3(b) shows an X-ray diffraction pattern of the alloy after the heat treatment, which indicates peaks assigned to crystal phases. It is evident from a tranmission electron photomicrograph (magnification: 300,000) of the heat-treated ribbon that most of the alloy structure of the ribbon after the heat treatment consists of fine crystalline particles. The crystalline particles had an average particle size of about 100~. From the analysis of the X-ray diffraction pattern and the transmission electron photomicrograph, it can be presumed that these crystalline particles are ~-Fe having Si, B, etc.
dissolved therein.
Next, the Fe-base soft magnetic alloy ribbons before and after the heat treatment were measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG
and a frequency of 100kHz. As a result, the core loss was 4100mW/cc before the heat treatment, while it was 240mW/cc after the heat treatment. Effective permeability ~e was also measured at a frequency of lkHz and Hm of 5mOe. As a result, the former tbefore the heat treatment) was 480, while the latter (after the heat treatment) was 10100.
Example 3 A melt having the composition (by atomic %) of 1% Cu7 16.5% Si, 6% B, 3% Nb and balance substantially Fe was formed into a ribbon of 5mm in width and 18~m in thickness by a single ~3~3219 roll method. The X-ray diffraction of this ribbon showed a halo pattern peculiar to an amorphous alloy, meaning that the resulting ribbon was almost completely amor~hous.
Next, this amorphous ribbon was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter~ and then heat-treated in a ni~rogen gas atmosphere at 550C for one hour. The X-ray diffraction of the heat-trea-ted ribbon showed peaks assigned to crystals composed of an Fe-solid solution having a bcc structure. It is evident from a transmission electron photomicrograph ~magnification: 300,000) of the heat treated ribbon that most of the alloy structure of the ribbon after the heat treatment consists of fine crystalline particles. It was observed that the crystalline particles had an average particle size o about lo0A.
Next, the Fe-base soft magnetic alloy ribbons before and after the heat treatment were measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG
and a frequency of 100kHz. As a result, the core loss was 4000mW/cc before the heat treatment, while it was 220mW/cc after the heat treatment. Effective permeability ~e was also measured at a frequency of lkHz and Hm of 5mOe. As a result, the former (before the heat treatment) was 500, while the latter (after the heat treatment) was 100200.
Next, the alloy of this Example containing both Cu and Nb was measured with respect to saturation mangetostriction ~s. It was +20.7x10 6 in an amorphous state before heat treatment, but it was reduced to +1.3x10 6 by heat treatment at 550C for one hour, much smaller than the mangetostriction of , ~
~23219 conventional Fe-base amorphous alloys.
E~ample 4 A melt having the composition (by atomic %) of 1% Cu, 13.8% Si, 8.9% B, 3.2% Nb, 0.5% Cr, 1% C and balance substantially Fe was formed into a ribbon of 10mm in width and 18~m in thickness by a single roll method. The X-ray diffraction of this ribbon showed a halo pattern peculiar to an amorphous alloy. The transmission electron photomicrograph (magnification: 300,000) o-f this ribbon shownd that the resulting ribbon was àlmost completely amorphous.
Next, this amorphous ribbon was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter, and then heat-trea-ted in a nitrogen gas atmosphere a-t 570C for one hour. It is evident from a tranmission electron photomicrograph (magnification: 300,000) of the ribbon after the heat treatment that most of the al].oy structure of the rihbon after the heat treatment consis~:s of fine crystalline particles. The crystalline particles had an average particle size of about lo0A.
~ext, the Fe-base soft magnetic alloy ribbons before and after the heat treatment were measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG
and a frequency of 100kHz. As a result, the core loss was 3800mW/cc before the heat treatment, while it was 240mW/cc after the heat treatment. Effective permeability ~e was also measured at a frequency of lkHz and Hm oE 5mOe. As a result, the former (before the heat treatment) was 500, while the latter (after the heat treatment) was 102000.
, : . , .. . ;
~32~2~9 Example 5 Fe-base amorphous alloys having the compositions as shown in Table 1 were prepared under the same conditions as in Example 1. The resulting alloys were classified into 2 groups, and those in one group were subjected to the same heat treatment as in Example 1, and those in the other group were subjected to a conventional heat treatment (400C x 1 hour) to keep an amorphous state. They were then measured with respect to core loss W2/1ook at 100kHz and 2kG and effective permeability ~elk at lkHz and Hm=5mOe. The results are shown in Table 1~
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~3~3219 Example 7 Fe-base amorphous alloys having the compositions as shown ln Table 3 were prepared under the same conditions as in Example 4. The resulting alloys were classified into 2 groups, and those in one group were subjected to the same heat treatment as in Example 4, and those in the other group were subjected to a conventional heat treatment (400C x 1 hour) to keep an amorphous state. They were then measured with respect to core loss W2/1ook at 100kHz and 2kG and effective permeability ~elk at lkHz and Hm=5mOe. The results are shown in Table 3.
Thus, it has been clarified that the heat treatment according to -the present invention can provide the alloy with low core loss and high effective permeability.
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r~ '~'~4 g ~\ V O (D O O O O O o o O O O
Therefore, an object of the present invention is to provide an Fe-base soft magnetic alloy having excellent magnetic characteristics such as core loss, time variability of core loss, permeability, etc.
Another object of the present invention is to provide an Fe-base soft magnetic alloy having excellent soft magnetic properties, particularly high-frequency magnetic properties, and also a low magnetostriction which keeps it from suffering ,, ~
, , , ,; : . ~, ~''''' ' ' :, :~ .
' ' ; ` :' ' ':, :: ' ~32~219 from magnetic deterioration by impregnation and deformation.
A further object of the present invention is to provide a method of producing such Fe-base soft magnetic alloys.
Intense research in view of the above objects has revealed that the addition of Cu and at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo to an Fe-base alloy having an essential composition of Fe-Si-B, and a proper heat treatment of the Fe-base alloy which is once made amorphous can provide an Fe-base soft magnetic alloy, a major part of which structure is composed of fine crystalline particles, and thus having excellent soft magnetic properties. It has also been found that by limiting the alloy composition properly, the alloy can have a low magnetostriction. The present invention is based on these findings.
Thus, the Fe-base soft magnetic alloy according to the present invention has the composition represented by the general formula:
(Fe M ) Cu Si B M' l-a a lO0-x-y-z-~ x y z wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, ~If, Ti and Mo, and a, x, y, 2 and ~ respectively satisfy O<a<0.5~ O.l<x<3, O<y<30, O<z<25, 5<y+z<30 and 0.1<~<30, at least 50% of the alloy structure being occupied by fine crystalline particles.
Another Fe-base soft magnetic alloy according to the present invention has the composition represented by the general formula:
"
..
::: ,, :::, 1~3219 ( l-a a)loo-x-y-z-~-~-ycuxsiyBzMl M~3X
wherein is M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, M~ is at least one element selected from the group consisting of V, Cr, Mn, A~, elements in the platinum group, Sc, Y, rare earth elements, Au, Zn, Sn and Re, X is at least one element selected from the group consisting of C, Ge, P, Ga, Sb, In, Be and As, and a, x, y, z, ~, ~ and y respectively satisfy 0<a<0.5, 0.1<x<3, 0<y<30, 0<z<25, 5<y+z<30, 0.1<~<30 ~<10 and y<l0, at least 50% of the alloy structure being fine crystalline particles having an average particle size of lo00A
or less.
Further, the method of producing an Fe-base soft magnetic alloy according to the present invention comprises the steps of rapidly quenching a melt of the above composition and heat treating it to generate fine crystalline particles.
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 (a) is a transmission electron photomicroscope (magnification: 300,000) of the Fe-base soft magnetic alloy after heat treatment in Example l;
Fig. 1 (b) is a schematic view of the photomicrograph of Fig. 1 (a);
Fig. 1 (c) is a transmission electron photomicrograph (magnification: 300,000) of the Fe-base soft magnetic alloy of Fe74 5Nb3Sil3 5Bg containing no Cu after heat treatment;
Fig. 1 (d) is a schematic view of the photomicrograph of Fig. 1 (c);
. .
-~ ~ . . , : .
~.
-132321~
Flg. 2 ls a transmission electron photomicrograph (magniflcatlon: 300,000) of the Fe-base soft magnetic alloy of Example 1 before heat treatment;
Fig. 3 (a) is a graph showlng an X-ray dlffraction pattern of the Fe-base soft magnetlc alloy of Example 1 before heat treatment;
Fig. 3 (b) ls a graph showing an X-ray diffraction pattern of the Fe-base soft magnetic alloy of the present inven-tion after heat treatment;
Flg. 4 (see the sheet of Flg. 2) is a graph showing the relatlons between Cu content (x) and core loss W2/10ok wlth re-spect to the Fe-base soft magnetlc alloy of Example g;
Flg. 5 ls a graph showlng the relatlons between M' con-tent (a) and core loss W2\10ok wlth respect to the Fe-base soft magnetlc alloy of Example 12;
Flg. 6 ls a graph showing the relatlons between M' con-tent la) and core loss W2~100k wlth respect to the Fe-base soft magnetic alloy of Example 137 Fig. 7 ls a graph showlng the relatlons between Nb con tent (a) and core loss W2/10ok wlth respect to the Fe-base soft magnetic alloy of Example 14r Flg. 8 ls a graph showlng the relations between frequen-cy and effectlve permeablllty with respect to the Fe-base soft magnetlc alloy of Example 15, the Co-base amorphous alloy and ferrlte; `;
Flg. 9 ls a graph showlng the relatlons between frequen-cy and effectlve permeabllity wlth respect to the Fe-base soft magnetic alloy of Example 16, Co-base amorphous alloy and ferrlte;
- . ,.. . .- ..
. . : , , ~
.,,, :,. , , - .. . .: ...
~323219 Fig. 10 is a graph showing the relations between frequency and ef~ective permeabllity with respect to the Fe-base soft maynet~c alloy of Example 17, Co-base amorphous alloy, Fe-base amorphous alloy and ferrlte;
Fig. 11 (see the sheet of Fig. 7) ls a graph showlng the relations between heat treatment temperature and core 1QSS with respect to the Fe-base soft magnetlc alloy of Example 20;
Fig. 12 is a graph showing the relatlons between heat treatment temperature and core loss with respect to the Fe-base soft magnetlc alloy of Example 21;
Fig. 13 is a graph showlng the relatlons between heat treatment temperature and effective permeablllty of the Fe-base soft magnetic alloy of Example 22;
Fig. 14 is a graph showing the relations between effec-tive permeability ~elk and heat treatment temperature with respect to the Fe-base soft magnetic alloy of E~xample 23;
Fig. 15 is a graph showing the relations betwe~n effec-t:lve permeability and hea-t treatment temperature with respect to the Fe-base soft magnetlc alloy of Example 24;
Fig. 16 (see the sheet of Fig. 13) ls a graph showing the relations between Cu content (x) and Nb content (a) and crystallization temperature with respect to the Fe-base soft magnetic alloy of Example 25;
Flg. 17 ls a graph showing wear after 100 hours of the Fe-base soft magnetic alloy of Example 26;
Fig. 18 is a graph showing the relatlons between Vickers hardness and heat treatment temperature with respect to the Fe-base soft magnetic alloy of ~xample 27;
'. ' ' ,~ ' ' ~ .
' ' ~ 323~
Fig. 19 is a graph showing the dependency of saturation magnetostriction (~s) and saturation magnetic flux density (Bs) on y with respect to the alloy of 73.5 1 3 y 22.5-y of Example 33;
Fig. 20 is a graph showing the saturation magnetostriction (~s) of the (Fe-Cul-Nb3~-Si-B pseudo-ternary alloy;
Fig. 21 is a graph showing the coercive force (Hc) of the (Fe-Cul-Nb3)-Si-B pseudo-ternary alloy;
Fig. 22 is a graph showing the effective permeability ~elk at lkHz of the (Fe-Cul-Nb3)-Si-B pseudo-ternary alloy;
Fig. 23 is a graph showing saturation magnetic flux density (Bs) of the (Fe-Cul-Nb3)-Si-B pseudo-ternary alloy;
Fig. 24 is a graph showing the core loss W2/1ook at lOOkHz and 2kG of the (Fe-Cul-Nb3)-Si-B pseudo-ternary alloy;
Fig. 25 is a graph showing the dependency oE magnetic properties on heat treatment with respect to the alloy of Example 35;
Fig. 26 is a graph showing the dependency of core loss on Bm in Example 37;
Fig. 27 is a graph showing the relations between core loss and frequency with respecat to the Fe-base soft magnetic alloy of the present invention, the conventional Fe-base amorphous alloy, the Co~base amorphous alloy and the ferrite in Example 38;
Figs. 28 ~a)-(d) are respectively graphs showing the direct current B-H curves of the alloys of the present invention in Example 39;
,... . .
'' :
, ~3232~9 Fig. 29 is a graph showing the X-ray diffraction pattern of the Fe-base soft magnetic alloy of Example 40;
Figs. 30 (a)-(c) are views each showing the direct current B-H curve of the Fe-base soft magnetic alloy of the present invention in Example 41;
Fig. 31 is a graph showing the relations between core loss and frequency with respect to the Fe-base soft magnetic alloy of the present invention and the conventional Co-base amorphous alloy in Example 41;
Fig. 32 is à graph showing the relations between magnetization and temperature with respect to the Fe-base soft magnetic alloy of Example 42; and Fig. 33 is a graph showing the heat treatment pattern of the Fe-base soft magnetic alloy of the present invention in Example 43.
DET~ILED DESCRIPTION OF THE INVENTION
In the Fe-base soft magnetic alloy of the present invention, Fe may be substituted by Co and/or Ni in the range of 0-0.5. However, to have good magnetic properties such as low core loss and magnetostriction, the content of Co and/or Ni which is represented by "a" is preferably 0-0.1. Particularly to provide a low-magnetostriction alloy, the range of ~a" is preferably 0-0.05.
In the present invention, Cu is an indispensable element, and its content "x" is 0.1-3 atomic %. When it is less than 0.1 atomic %, substantially no effect on the reduction of core loss and Oll the increase in permeability can J : :
~L323219 be obtained by the addition of Cu. On the other hand, when it exceeds 3 atomic %, the alloy's core loss becomes larger than those containing no Cu, reducing the permeability, too. The preferred content of Cu in the present invention is ~.5-2 atomic %, in which range the core loss is particularly small and the permeability is high.
The reasons why the core loss decreases and the permeability increases by the addition of Cu are not fully clear, but it may be presumed as follows:
Cu and Fe hàve a positive interaction parameter so that their solubility is low. However, since iron atoms or copper atoms tend to gather to form clusters, thereby producing compositional fluctuation. This produces a lot of domains likely to be crystallized to provide nuclei for generating Eine crystalline particles. These crystalline particles are based on Fe, and since Cu is substantially not soluble in Fe, Cu is ejected from the fine crystalline particles, whereby the Cu content in the vicinity of the crystal].ine particles becomes high. This presumably suppresses the growth oE crystalline particles.
Because of the formation of a large number of nuclei and the suppression of the growth of crystalline particles by the addition of Cu, the crystalline particles are made fine, and this phenomenon is accelerated by the inclusion of Nb, Ta, W, Mo, Zr, Hf, Ti, etc.
Without Nb, Ta, W, Mo, Zr, Hf, Ti, etc., the crystalline particles are not fully made fine and thus the soft magnetic properties of the resulting alloy are poor.
:. i`: ~ ' , :, ~ ,, ; , . ; ! , ', ~
: ~ ~ '`:
~3232~9 Particularly Nb and Mo are eEfective, and particularly Nb acts to keep the crystalline particles fine, thereby providing excellent soft magnetic properties. And since a fine crystalline phase based on Fe is formed, the Fe-base soft magnetic alloy of the present invention has smaller magnetostriction than Fe-base amorphous alloys, which means that the Fe-base soft magnetic alloy of the present invention has smaller magnetic anisotropy due to internal stress-strain, resulting in improved soft magnetic properties.
Without the addition of Cu, the crystalline particles are unlikely to be made fine. Instead, a compound phase is likely to be formed and crystallized, thereby deteriorating the magnetic properties.
Si and B are elements particular].y for making fine the alloy structure. The Fe-base soft magnetic alloy of -the present invention is desirably produced by once forming an amorphous alloy with the addition of Si and B, and then forming fine crystalline particles by heat treatment.
The content of Si ("y") and that of B ("z~) are O<y<30 atomic %, O<z<25 atomic %, and 5<y+z<30 atomic %, because the alloy would have an extremely reduced saturation magnetic flux density if otherwise.
In the present invention, the preferred range of y is 6-25 atomic %, and the preferred range of z is 2-25 atomic %, and the preferred range of y~z is 14-30 atomic %. When y exceeds 25 atomic %, the resulting alloy has a relatively large magnetostriction under the condition of good soft magnetic properties, and when y is less than 6 atomic %, sufficient soft .
, . . . -,~
,:
:: . .
:. :
~23219 magnetic properties are not necessarily obtained. The reasons for limiting the content of B ("z~) is that when z is less than 2 atomic %, uniform crystalline particle structure cannot easily be obtained, somewhat deteriorating the soft ma~netic properties, and when z exceeds 25 atomic %, the resulting alloy would have a relatively large magnetostriction under the heat treatment condition of providing good soft magnetic properties.
With respect to the total amount of Si+B (y+z), when y+z is less than 14 atomic %, it is often difficult to make the alloy amorphous, providing relatively poor magnetic properties, and when y+z exceeds 30 atomic % an extreme decrease in a saturation magnetic flux density and the deterioration of soft magnetic properties and the increase in magnetostriction ensue.
More preferably, the contents of Si and B are lO<y<25, 3<z<18 and 18<y+z<28, and this range provides the alloy with excellent soft magnetic properties, particularly a saturation ~agnetostriction in the range of -5xlO 6 _ +5xlO 6.
Particularly preferred range is ll<y<24, 3<z<9 and 18<y+z<27, and this range provides the alloy with a saturation magnetostriction in the range of -1.5xlO 6 _ +1.5xlO 6.
In the present inventionS M' acts when added together with Cu to make the precipitated crystalline particles fine.
M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo. These elements have a function of elevating the crystallization temperature of the alloy, and synergistically with Cu having a function of forming clusters and thus lowering the crystallization temperature, it suppresses the growth of the precipitated crystalline - . ,, .
.:
.
: :
~3~32~
particles, thereby making them fine.
The content Oc M' (~) is 0.1-30 atomic %. When it is less than 0.1 atomic %, sufficient effect of making crystalline particles fine cannot be obtained, and when it exceeds 30 atomic % an extreme decrease in saturation magnetic flux density ensues. The preferred content of M' is 0.1-10 atomic %, and more preferably ~ is 2-8 atomic %, in which range paxtieularly exeellent soft magnetie properties are obtained.
Ineidentally, most preferable as M' is Nb and/or Mo, and partieularly Nb in terms of magnetie properties. The addition of M' provides the Fe-base soft magnetie alloy with as high permeability as that of the Co-base, high-permeability materials.
M", which is at least one element seleeted from the group eonsisting of V, Cr, Mn, AQ, elements in the platinum group, Se, Y, rare earth elements, Au, Zn, Sn and Re, may be added for the purposes of improving eor.rosion resistanee or magnetie properties and of adjusting magnetostrietion, but its content is at most 10 atomie %. When the eontent of M~ exceeds 10 atomie %, an extremely deerease in a saturation magnetie flux density ensues. A particularly preferred amount of M~ is 5 atomie % or less.
Among them, at least one element selected from the group eonsisting of Ru, Rh, Pd, Os, Ir, Pt, Au, Cr and V is eapable of providing the alloy with particularly excellent eorrosion resistanee and wear resistanee, thereby making it suitable for magnetie heads, etc.
The alloy of the present invention may contain 10 atomic % or less of at least one element X selected from the group consisting of C, Ge, P, Ga, Sb, In, Be, As. These elements are effective for making amorphous, and when added with Si and s, they help make the alloy amorphous and also are effective for adjusting the magnetostriction and Curie temperature of the alloy.
In sum, in the Fe-base soft magnetic alloy having the general formula:
l-a a)loo-x-y-æ-~cuxsiyB M~ , the general ranges of`a, x, y, z and a are O<a~0.5 O.l<x<3 O<y<30 O<z<25 5<y+z<30 0.1<~<30, and the preferred ranges thereof are O<a<0.1 O.l<x<3 6<y<25 2<z<25 14<y+z<30 O . 1<~<10, and the more preferable ranges are O<a<0.1 0.5<x<2 lO<y<25 3<z<18 , . ..
;
.
~3232~9 l~<y~z<28 2<a<8, and the most preferable ranges are O~a<0.05 0.5<x<2 ll<y<24 3<z<9 18<y+z<27 2<a<8.
And in the Fe-base soft magnetic alloy having the general formula:
l-a a)loo_x_y_z_a_~_yCUxSiyB M' M7~X , the general ranges of a, x, y, z, a, ~ and y are O<a<0.5 O.l<x<3 O<y<30 O<z<25 5<y+z<30 O.l<a<30 ~<10 y<10, and the preferred ranges are O<a<0.1 O.l<x<3 6<y<25 2<z<25 14<y+z<30 O.l<a<10 . ~ -- ..
,., .. ,, ~ ~
: - . :.. ,, ~ . :
.... . : . . .: ;.
~323219 ~5 y<5, and the more preferable ranges are O~a<0.1 0.5<x<2 lO<y< 5 3<z<18 18<y+z<28 2<~<8 ~<5 y<5~
and the most preEerable ranges are O<a<0.05 0 5<x<2 ll<y<24 3<z<9 18<y+z<27 2<a<8 .
~<5 ~_ The Fe-base soft magnetic alloy having the above composition according to the pr~sent invention has an alloy structure, at least 50% of which consists of fine crystalline particles. These crystalline particles are based on a-Fe having a bcc structure, in which Si and B, etc. are dissolved.
These crystalline particles have an extremely small average particle siæe of looOA or less, and are uniformly distributed in the alloy structure. Incidentally, the average paticle size :,:
. . : , : ,. ~ :
j . . . .
- : .: ,;, ;
~32~2~9 of the crystalline particles is determined by measuring the maximum size of each particle and averaging them. When the average particle size exceeds loOOA, good soft magnetic properties are not obtained. It is preferably 500~ or less, more preferably 200~ or less and particularly 50-200A. The remaining portion of the alloy structure other than the fine crystalline particles is mainly amorphous. Even with fine crystalline particles occupying substantially 100% of the alloy structure, theFe-base soft magnetic alloy of the present invention has sufficiently good magnetic properties.
Incidentally, with respect to inevitable impurities such as N, O, S, etc., it is to be noted that the inclusion thereof in such amounts as not to deteriorate the desired properties is not regarded as changing the alloy composition of the present invention suitable for magnetic cores, etc.
Next, the method of producing the Fe-base soft magnetic alloy of the present invention will be explained in detail below.
First, a melt of the above composition is rapidly quenched by known liquid quenching methods such as a single roll method, a double roll method, etc. to ~orm amorphous alloy ribbons. Usually amorphous alloy ribbons produced by the single roll method, etc. have a thickness of 5-lOO~m or so, and those having a thickness of 25~m or less are particularly suitable as magnetic core materials for use at high frequency.
These amorphous alloys may contain crystal phases, but the alloy structure is preferably amorphous to make sure the formation of uniform fine crystalline particles by a . :
: . ~:
. : , - : .
: .. :.::: - . :. ;
:: . . . . .
. .
:~
: , .
: . :
~3232~
subsequent heat treatment. Incidentally, the alloy of the present invention can be produced directly by the liquid quenching method without resorting to heat treatment, as long as proper conditions are selected.
The amorphous ribbons are wound, punched, etched or subjected to any other working to desired shapes before heat treatment, for the reasons -that the ribbons have good workability in an amorphous state, but that once crystallized they lose workability.
The heat treatment is carried out by heating the amorphous alloy ribbon worked to have the desired shape in vaccum or in an inert gas atmosphere such as hydrogen, nitrogen, argon, etc. The temperature and time of the heat `
treatment varies depending upon the composition of the amorphous alloy ribbon and the shape and size of a magnetic core made from the amorphous alloy ribbon, etc., but in general it is preferably 450-700C for 5 minutes to 24 hours. When the heat treatment temperature is lower than 450C, crystallization is unlikely to take place with ease, requiring too much time for the heat treatment. On the other hand, when it exceeds 700C, coarse crystalline particles tend to be formed, making it difficult to obtain fine crystalline particles. And with respect to the heat treatment time, when it is shorter than 5 minutes, it is difficult to heat the overall worked alloy at uniorm temperature, providing uneven magnetic properties, and when it is longer than 24 hours, productivity becomes too low and also the crystalline particles grow excessively, resulting in the deterioration of magnetic properties. The preferred ,. , .:
.
:
~3232~ 9 heat treatment conditions are, taking into consideration practicality and uniform temperature control, etc., 500-650C
for 5 minutes to 6 hours.
The heat treatment atmosphere is preferably an inert gas atmosphere, but it may be an oxidizing atmosphere such as the air. Cooling may be carried out properly in the air or in a furnace. And the heat treatment may be conducted by a plurality of steps.
The heat treatment can be carried out in a magnetic field to provide the alloy with magnetic anisotropy. When a magnetic field is applied in parallel to the magnetic path o~ a magnetic core made of the alloy of the present invention in the heat treatment step, the resulting heat-treated magnetic core has a good squareness in a 3-H curve thereof, so that it is particularly suitable for saturable reactors, magnetic switches, pulse compression cores, reactors for preventing spike voltage, etc. On the other hand, when the heat treatment is conducted while applying a magnetic field in perpendicular to the magnetic path of a magnetic core, the B-H curve inclines, providing it with a small squareness ratio and a constant permeability. Thus, it has a wider operational range and thus is suitable for transformers, noise filters, choke coils, etc.
The magnetic field need not be applied always during the heat treatment, and it is necessary only when the alloy is at a temperature lower than the Curie temperature Tc thereof.
In the present inven-tion, the alloy has an elevated Curie temperature because of crystallization than the amorphous . .. : .; :
: :: . : . .......... .
, :, .. .
, -::`. : ~
~32~219 counterpart, and so the heat treatment in a magnetic field can be carried out at temperatures higher than the Curie temperature of the corresponding amorphous alloy. In a case of the heat treatment in a magnetic field, it may be carried out by two or more steps. Also, a rotational magnetic field can be applied during the heat treatment.
Incidentally, the Fe-base soft magnetic alloy of the present invention can be produced by other methods than liquid quenching methods, such as vapor deposition, ion plating, sputtering, etc. which are suitable for producing thin-film magnetic heads, etc. Further, a rotation liq~id spinning method and a glass-coated spinning method may also be utilized toproduce thin wires.
In addition, powdery products can be produced by a cavitation method, an atomization method or by pulveri2ing thin ribbons prepared by a single roll method, etc.
Such powdery alloys of the present invention can be compressed to produce dust cores or bul]~y products.
When the alloy of the present invention is used for magnetic cores, the surface of the alloy is preperably coated with an oxidation layer by proper heat treatment or chemical treatment, or coated with an insulating layer to provide insulation between the adjacent layers so that the magnetic cores may have good properties.
The present invention will be explained in detail by the following Examples, without intention of restricting the ;-scope of the present invention.
Example 1 , , -:, ' , ' ' , ,: .~: ~' ;
1~232~9 A melt having the composition ~by atomic %) of 1%
Cu, 13.4% Si, 9.1% B, 3.1% Nb and balance substantially Fe was formed into a ribbon of 5mm in width and 18~m in thickness by a single roll method. The X-ray diffraction of this ribbon showed a halo pattern peculiar to an amorphous alloy. A
transmission electron photomicrograph (magnification: 300,000) of this ribbon is shown in Fig. 2. As is clear from the X-ray diffraction and Fig. 2, the resulting ribbon was almost completely amorphous.
Next, this àmorphous ribbon was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter, and then heat-treated in a nitrogen gas atmosphere at 550C for one hour. Fig. l(a) shows a transmission electron photomicrograph (magnification: 300,000) of the heat-treated ribbon. Fig. l(b) schematically shows the fine crystalline particles in the photomicrograph of Fig. l(a). It is evident from Figs. 1 (a) and (b) that most. of the alloy structure of the ribbon after the heat treatment consists of fine crystalline particles. It was also confirmed by X-ray diffraction that the alloy after the heat treatment had crystalline particles. The crystalline particles had an average particle size of about loOA. For comparison, Fig. l(c) shows a transmission electron photomicrograph (magnification:
300,000) of an amorphous alloy of Fe74 5Nb3Sil3 5Bg containing no Cu which was heat-treated at 550C for 1 hour, and Fig. l(d) schematically shows i-ts crystalline particles.
The alloy of the present invention containing both Cu and Nb contains crystalline particles almost in a spherical ; , :
: ~ : . ~ .:: . :
: . ~ . : - i . .:. . :.
: .
~32S-3219 shape having an average particle size of about looA. On the other hand, in alloys containing only Nb without Cu, the crystalline particles are coarse and most of them are not in the spherical shape. It was confirmed that the addition of both Cu and Nb greatly affects the size and shape of the resulting crystalline particles.
Next, the Fe-base soft magnetic alloy ribbons before and after the heat treatment were measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2k5 and a frequency of 100kMz. As a result, the core loss was 4000mW/cc before the heat treatment, while it was 220m~/cc after the heat treatment. Effective permeability ~e was also measured at a frequency of lkHz and Hm of 5mOe. As a result, the former (before the heat treatment) was 500, while the latter (after the heat treatment) was 100200. This clearly shows that the heat trea-tment according to the present invention serves to form fine crystalline particles uniformly in the amorphous alloy structure, thereby extremely lowering core loss and enhancing permeability.
Example 2 A melt having the composition (by atomic %) of 1% Cu, 15% Si, 9% B, 3% Nb, 1% Cr and balance substantially Fe was formed into a ribbon of 5mm in width and 18~1m in thickness by a single roll method. The X-ray diffraction of this ribbon showed a halo pattern peculiar to an amorphous alloy as is shown in Fig. 3(a). As is clear from a transmission electron photomicrograph (magnification: 300,000) of this ribbon and the X~ray diffraction shown in Fig~ 3(a), the resulting ribbon ,. -- . .. , ~ : .
' " ' "" ' ' ' ' ' ., ,. . ' ~' ' ' ~ .-. .. .
~ 3 2 1 21 !~
was almost completely amorphous.
Next, this amorphous ribbon was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter, and then heat-treated in the same manner as in Example 1. Fig. 3(b) shows an X-ray diffraction pattern of the alloy after the heat treatment, which indicates peaks assigned to crystal phases. It is evident from a tranmission electron photomicrograph (magnification: 300,000) of the heat-treated ribbon that most of the alloy structure of the ribbon after the heat treatment consists of fine crystalline particles. The crystalline particles had an average particle size of about 100~. From the analysis of the X-ray diffraction pattern and the transmission electron photomicrograph, it can be presumed that these crystalline particles are ~-Fe having Si, B, etc.
dissolved therein.
Next, the Fe-base soft magnetic alloy ribbons before and after the heat treatment were measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG
and a frequency of 100kHz. As a result, the core loss was 4100mW/cc before the heat treatment, while it was 240mW/cc after the heat treatment. Effective permeability ~e was also measured at a frequency of lkHz and Hm of 5mOe. As a result, the former tbefore the heat treatment) was 480, while the latter (after the heat treatment) was 10100.
Example 3 A melt having the composition (by atomic %) of 1% Cu7 16.5% Si, 6% B, 3% Nb and balance substantially Fe was formed into a ribbon of 5mm in width and 18~m in thickness by a single ~3~3219 roll method. The X-ray diffraction of this ribbon showed a halo pattern peculiar to an amorphous alloy, meaning that the resulting ribbon was almost completely amor~hous.
Next, this amorphous ribbon was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter~ and then heat-treated in a ni~rogen gas atmosphere at 550C for one hour. The X-ray diffraction of the heat-trea-ted ribbon showed peaks assigned to crystals composed of an Fe-solid solution having a bcc structure. It is evident from a transmission electron photomicrograph ~magnification: 300,000) of the heat treated ribbon that most of the alloy structure of the ribbon after the heat treatment consists of fine crystalline particles. It was observed that the crystalline particles had an average particle size o about lo0A.
Next, the Fe-base soft magnetic alloy ribbons before and after the heat treatment were measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG
and a frequency of 100kHz. As a result, the core loss was 4000mW/cc before the heat treatment, while it was 220mW/cc after the heat treatment. Effective permeability ~e was also measured at a frequency of lkHz and Hm of 5mOe. As a result, the former (before the heat treatment) was 500, while the latter (after the heat treatment) was 100200.
Next, the alloy of this Example containing both Cu and Nb was measured with respect to saturation mangetostriction ~s. It was +20.7x10 6 in an amorphous state before heat treatment, but it was reduced to +1.3x10 6 by heat treatment at 550C for one hour, much smaller than the mangetostriction of , ~
~23219 conventional Fe-base amorphous alloys.
E~ample 4 A melt having the composition (by atomic %) of 1% Cu, 13.8% Si, 8.9% B, 3.2% Nb, 0.5% Cr, 1% C and balance substantially Fe was formed into a ribbon of 10mm in width and 18~m in thickness by a single roll method. The X-ray diffraction of this ribbon showed a halo pattern peculiar to an amorphous alloy. The transmission electron photomicrograph (magnification: 300,000) o-f this ribbon shownd that the resulting ribbon was àlmost completely amorphous.
Next, this amorphous ribbon was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter, and then heat-trea-ted in a nitrogen gas atmosphere a-t 570C for one hour. It is evident from a tranmission electron photomicrograph (magnification: 300,000) of the ribbon after the heat treatment that most of the al].oy structure of the rihbon after the heat treatment consis~:s of fine crystalline particles. The crystalline particles had an average particle size of about lo0A.
~ext, the Fe-base soft magnetic alloy ribbons before and after the heat treatment were measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG
and a frequency of 100kHz. As a result, the core loss was 3800mW/cc before the heat treatment, while it was 240mW/cc after the heat treatment. Effective permeability ~e was also measured at a frequency of lkHz and Hm oE 5mOe. As a result, the former (before the heat treatment) was 500, while the latter (after the heat treatment) was 102000.
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~32~2~9 Example 5 Fe-base amorphous alloys having the compositions as shown in Table 1 were prepared under the same conditions as in Example 1. The resulting alloys were classified into 2 groups, and those in one group were subjected to the same heat treatment as in Example 1, and those in the other group were subjected to a conventional heat treatment (400C x 1 hour) to keep an amorphous state. They were then measured with respect to core loss W2/1ook at 100kHz and 2kG and effective permeability ~elk at lkHz and Hm=5mOe. The results are shown in Table 1~
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~3~3219 Example 7 Fe-base amorphous alloys having the compositions as shown ln Table 3 were prepared under the same conditions as in Example 4. The resulting alloys were classified into 2 groups, and those in one group were subjected to the same heat treatment as in Example 4, and those in the other group were subjected to a conventional heat treatment (400C x 1 hour) to keep an amorphous state. They were then measured with respect to core loss W2/1ook at 100kHz and 2kG and effective permeability ~elk at lkHz and Hm=5mOe. The results are shown in Table 3.
Thus, it has been clarified that the heat treatment according to -the present invention can provide the alloy with low core loss and high effective permeability.
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Example 8 Thin amorphous alloy ribbons of 5mm in width and 18~m in thickness and having the compositions as shown in Table 4 were prepared by a single roll method, and each of the ribbons was wound into a toroid of l9mm in outer diameter and 15mm in inner diameter, and then heat-treated at temperatures higher than the crystallization temperature. They were then measured with respect to DC magnetic properties, effective permeability ~elk at lkHz and core loss 2/lOOk Saturation magnetization ~s was also measured. The results are shown in Table 4.
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~323~9 Table 4 Sample Composition Bs (KG) Hc (Oe) ~elk W2 0 As 6 No. (at ~) (m~CC~ (X10 l Fe74Cu0 sSil3.5B9 3 12.40.01368000 300 +1.8 2 Fe74CU1 5Sil3.5BgN 2 12.6 0.015 76000 230 +2.0 79 1.0 8 9 3 14.60.05621000 470 +1.8 4 Fe74 5Cul oSil3.5 65 11.60.02042000 350 +1.5 Fe77CUl.oSiloB9N 3 14.30.02548000 430 +1.6 6 Fe73 5Cul oSil7.5B53 10.50.01542000 380 -0.3 7 Fe71CU1 5Sil3.5B9 5 11.20.01268000 280 +1.9 8 Fe74Cul oSil4 8 3 12.10.02274000 250 ~1.7 g Fe73Cu2 oSil3.s 8.53 11.60.02829000 350 +2.0 Fe74 5Cul osil3.5B9Ta2 12.80.01833000 480 +1.8 11 Fe72Cul oSil4 8 511.7 0.030 28000 380 +2.0 12 Fe71 5Cul osil3.5B9T 5 11.30.03828000 480 +1.8 13 Fe73Cul 5Sil3.5B9M 3 12.10.01469000 250 +2.8 14 Fe73 5Cul oSil3.5B93 11.4 0.017 43000 330 +1.9 Fe71Cul oSil3 10 5 10.0 0.023 68000 320 +2.5 16 e78 9 13 P 15.6 0.0350003300 +2.7 17 70.3 4.7 15 10 P 8.0 0.006 8500 350 ~ 0 18 Fe84 2sig.6A~6.2 11.0 0.02 10000 - ~ 0 -Note: Nos,16-18 Conventional alloys , . " .; . . i "
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~232~9 Example 9 Each of amorphous alloys having the composition of Fe74 5 xCuxNb3Sil3 5Bg (O<x<3.5) was heat-treated at the following optimum heat treatment temperature for one hour7 and then measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG and a frequency f=lOOkHz.
X (atomic %)Heat Treatment Temperature (C) 10 0.05 500 0.1 520 0.5 540 1.0 550 1.5 550 2.0 540 2.5 ~30 3.0 500 3.2 500 3.5 490 The relations between the content x of Cu (atomic %) and the core loss W2/1ook are shown in Fig. 4. It is clear from Fig. 4 that the core loss decreases as the Cu content x increases from 0, but that when it exceeds about 3 atomic %, the core loss becomes as large as that of alloys containing no Cu. When x is in the range of 0.1-3 atomic %, the core loss is sufficiently small. Particularly desirable range of x appears to be 0.5-2 atomic %.
Example 10 ~3~3219 Each of amorphous alloys having the composition of Fe73_xCUxSil4BgNb3Crl (O<x<3-5) was heat-treated at the following optimum heat treatment temperature for one hour, and then measured with respect to core loss W2/1ook at a wave height of magnetic flux density sm=2kG and a frequency f=lOOkHz.
Heat Treatment Temperature Core Loss X (atomic %) (C) W2/lOOk (mW/cc) o 505 980 0.05 510 900 0.1 520 610 1.0 560 210 1.5 560 230 2.0 550 250 2.5 530 390 3.0 500 630 3.2 500 850 3.5 490 1040 It is clear from the above that the core loss deereases as the Cu eontent x inereases from 0, but that when it exceeds about 3 atomic %, the eore loss becomes as large as that of alloys containing no Cu. When x is in the range of ~ 3 ato~ic %, the core loss is su~iciently small.
Partieularly desirable range of x ap~ears to be 0.5-2 atomie %.
Example 11 Each of amorphous alloys having the composition of Fe69_xCUxSil3.5B9 5Nb5Cr1C2 (O<x<3.5) was heat-treated at the , , ' ' 132~.~2~
following optimum heat treatment temperature for one hour, and then measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG and a frequency f=lOOkHz.
Heat Treatment Temperature Core Loss X (atomic %) (C) W2/lOOk (mW/cc) 0.1 535 560 0.5 550 350 1.0 590 240 1.5 580 240 2.0 570 290 2.5 560 440 3.0 550 630 3.2 540 860 It is cLear from the above that the core loss decreases as the Cu content x increase~; from 0, but that when it exceeds about 3 atomic %, the core :Loss becomes as large as that of alloys containing no Cu. When x is in the range of 0.1-3 atomic %, the core loss is sufficiently small.
Particularly desirable range of x appears to be 0.5-2 atomic %.
Example 12 Each of amorphous alloys having the composition of Fe76 5 CulSi13B9 5M' (M'=Nb, W, Ta or Mo) was heat-tr~ated at the following optimum heat treatment temperature for one hour, and then measured with respect to core loss W2/1ook.
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a (atomic %) Heat Treatment Temperature (C) 0.1 405 0.2 410 1.0 430 2.0 ~80 3.0 550 5.0 580 7.0 590 8.0 `590 10.0 590 11.0 590 The results are shown in Fig. 5, in which graphs A, B, C and D show the cases where M' is Nb, W, Ta and Mo, respectively.
As is clear from Fig. 5, the core loss is sufiiciently small when the amount ~ oi.- M' is in the range of 0.1-10 atomic %. And particularly when M' is Nb, the core loss ~`
was extremely low. A particularly des:ired range oE a is 2<~<8.
Example 13 Each of amorphous alloys having the composition of Fe75 5 CulSil3B9 5M'~Til (M'=Nb, W, Ta or Mo) was heat-treated at the following optimum heat treatment temperature for one hour, and then measured with respect to core loss W2/1ook.
a (atomic %)Heat Treatment Temperature (C) 0.1 410 0.2 420 ,,, . ! , ~
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As is clear from Fig. 6, the core loss is sufficiently small when the amount a of ~' is in the range of 0.1-10 atomic %. And particularly when M' is Nb, the core loss was extremely low. A particularly desired range of a is 2<a<8.
_xample 14 Each of amorphous alloys havi.ng the composition of Fe75 CulSil3BgNb RulGel was heat-treat:ed at the following optimum heat treatment temperature for one hour, and then 20 measured with respect to core loss W2/1OOk.
a (atomic %)Heat Treatment Temperature (C) 0.1 410 0.2 415 1.0 430 2.0 485 3.0 555 S.0 585 .
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~323219 7.0 595 8.0 595 10.0 595 11.0 595 The results are shown in Fig. 7. As is clear from Fig. 7, the core loss is sufficiently small when the amount a of Nb is in the range of 0.1-10 atomic %. A particularly desired range of ~ is 2<~<8.
Incidentally, the electron microscopy showed that fine crystalline particles were generated when a was Ool or more.
Example 15 Each oE amorphous alloys having the composition of Fe73.5CulNb3Sil3~9 5 was heat-treated at 550C for one hour.
Their transmission electron microscopy revealed that each of them contained 50% or more of a crystal phase. They were measured with respect to effective permeability ~e at frequency o~ 1 - lxlO"KHz. Similarly? a Co-base amorphous alloy (Co69 6FeO 4Mn6Sil5Bg) and Mn-Zn ferrite were measured with respect to effective permeability ~e. The results are shown in Fig~ 8, in which graphs A, B and C show the heat treated Fe-base soft magnetic alloy of the present invention, the Co-base amorphous alloy and the ferrite, respectively.
Fig. 8 shows that the Fe-base soft magnetic alloy of the present invention has permeability equal to or higher than that of the Co-base amorphous alloy and extremely higher than that of the ferrite in a wide frequency range. Because o~
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Example 16 Each of amorphous alloys having the composition of Fe72CulSil3 5B9 5Nb3Rul was heat-treated at 550C for one hour.
Their transmission electron microscopy revealed that each of them contained 50% or more of a crystal phase. They were measured with respect to effective permeability ~e at a frequency of 1 - lx104KHz. Similarly a Co-base amorphous alloy (Co69 6FeO 4Mn6Sil5Bg) and Mn-Zn ferrite were measured with respect to effective permeability ~e. The results are shown in Fig. 9, in which graphs A, B and C show the heat-treated Fe-base soft magnetic al].oy of the present invention, the Co-base amorphous alloy and the Eerrite, respectively.
Fig. 9 shows that the Fe-base soft magnetic alloy of the present invention has permeability equal to or higher than that of the Co-base amorphous alloy ancl extremely higher than that of the Eerrite in a wide frequency range.
Example 17 Each of amorphous alloys having the composition o-f Fe71CulSil5B8~b3ZrlPl was heat-treated at 550C for one hour.
Their transmission electron microscopy revealed that each of them contained 50% or more of a crystal phase and then measured with respect to effective permeability ~e at frequency of 1 -lx104KHz. Similarly a Co-base amorphous alloy (co66Fe4~i3Mo2silsBlo)~ an Fe-base amorphous ~lloy (Fe77CrlSil3Bg), and Mn-Zn ferrite were measured with respect to effective permeability ~e. The results are shown in Fig.
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~323219 10, in which graphs A, B, C and D show the heat-treated Fe-base soft magne-tic alloy of the present invention, the Co-base amorphous alloy, the Fe-base amorphous alloy and the ferrite, respectively.
Fig. 10 shows that the Fe-base soft magnetic alloy of the present invention has permeability equal to or higher than that of the Co-base amorphous alloy and extremely higher than that of the Fe-base amorphous alloy and the ferrite in a wide frequency range.
Example 18 Amorphous alloys having the compositions as shown in Table 5 were prepared under the same conditions as in Example 1, and on each alloy the relations between heat treatment conditions and the time variability of core loss were investigated. One heat trea-tment condition was 550C for one hour (according to the present invention), and the other was 400C x 1 hour tconventional method). It was confirmed by electron microscopy that the Fe-base soft magnetic alloy heat-treated at S50C for one hour according to the present invention contained 50% or more of fine crystal phase.
Incidentally, the time variation of core loss (W100-W~)/Wo was calculated from core loss (W0) measured immediately after the heat treatment of the present invention and core loss (W100) measured 100 hours after keeping at 150C, both at 2kG and 100kHz. The results are shown in Table 5.
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Alloy Compositlon Heat Treatment of Conventional No. (atomic %) Present Invention Heat Treatment 1 Fe71CUl b3 10 lS
2 Fe70 5Cul sNbsSillB12 3 Fe70 5Cul 5M5Sil3B10 4 Co69Fe4Nb2Sil5B10 1.22 Co69 5Fe4.5M25il5 9 1.30 The above results show that the heat treatment of the present invention reduces the time variation of core loss ~Nos.
1-3). Also it is shown that as compared with the conventional, low-core loss Co-base amorphous alloys (Nos. 4 and 5), the Fe-base soft magnetic alloy of the present invention has extremely reduced time variation of core loss. There~ore, the Fe--base soft magnetic alloy of the present invention can be used Eor highly reliable magnetic parts.
Example 19 Amorphous alloys having the composition as shown in Table 6 were prepared under the same conditions as in Example 1, and on each alloy the relations between heat treatment conditions and Curie t`emperature (Tc) were investigated. One heat treatment condition was 550C x 1 hour (present invention), and the other heat treatment condition was 350~C x 1 hour (conventional method). In the present invention, the Curie temperature was determined from a main phase (fine crystalline particles) occupying most of the alloy structure.
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~3~32~9 It was confirmed by X-ray diffraction that those subjected to heat trea-tment at 350C for 1 hour showed a halo pattern peculiar to amorphous alloys, meaning that they were substantially amorphous. On the other hand, those subjected to heat treatment at 550C for 1 hour showed peaks assigned to crystal phases, showing substantially no halo pattern. Thus, it was confirm that they were substantially composed of crystalline phases. The Curie temperature ~Tc) measured in each heat treatment is shown in Table 6.
Table 6 Curie Temperature (C) Alloy Composition Heat Treatment of Conventional No. (atomic %) Present Invention Heat Treatment 1 Fe73 sCU1Nb3Sil3.5 9 567 340 2 Fe71CU1 5Nb5Sil3.5 9 560 290 3 Fe71 sCUlMsSil3.5 9 560 288 4 Fe74CulTa3sil2Blo 565 334 Fe71 5CUlw5sil3.5 9 561 310 The above results show that the heat treatment of the present invention extremely enhances the Curie temperature (Tc). Thus, the alloy of the present invention has magnetic properties less variable with the temperature change than the amorphous alloys. Such a large difference in Curie temperature between the Fe-base soft magnetic alloy of the present invention and the amorphous alloys is due to the fact that the alloy subjected to the heat treatment of the present lnven-tion /
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132'321L9 is finely crystallized.
Exampled 20 A ribbon of an amor~hous alloy having the composition of Fe74 5 xCuxNb3Sil3 5~9 (width: 5mm and thickness: 18~m) was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter and heat-treated at various temperatures for one hour. Core loss W2/1ook at 2kG and lOOkHz was measured on each of them. The results are shown in Fig. 11.
The crystallization temperatures (Tx) of the amorphous alloys used for the wound cores were measured by a differential scanning calorimeter (DSC). The crystallization temperature Tx measured at a temperature-elevating speed of 10 C/minute on each alloy were 583C for x=0 and 507C for x=0.5, 1.0 and 1~5.
As is clear from Fig. 11, when the Cu content x is 0, core loss W2/1ook is extremely large, and as the Cu content increases up to about 1.5 atomic %, the core loss becomes small and also a proper heat treatment temperature range becomes as higher as 540-580C, exceeding that of those containing no Cu.
~his temperature is higher than the crystallization temperature Tx measured at a temperature~elevating speed of 10 C/minute by DSC. Incidentally, it was confirmed by transmission electron microscopy that tlle Fe-base soft magnetic alloy of the present invention containing Cu was constituted by 50% or more of fine crystalline particles.
Example 21 A ribbon of an amorphous alloy having the composition of Fe73 Cu Sil3BgNb3CrlCl (width: 5mm and thickness: 18~m) was .; . .. -. ~.: ::
:
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, : ~ . . ::: ~ :
: . :, ,: ~
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, : ~: . . .
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~32~2~9 formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter and heat-treated at various temperatures for one hour. Core loss W2/1ook at 2kG and lOOkH~ was measured on each of them. The results are shown in Fig. 12.
The crystallization temperatures (Tx) of the amorphous alloys used for the wound cores were measured by a differential scanning calorimPter ~DSC). The crystallization temperatures Tx measured at a temperature-elevating speed of 10 C/minute on each alloy were 580C for x=0 and 505C for x=0.5, 1.0 and 1.5.
As is clear from Fig. 12, when the Cu content x is 0, core loss W2/1ook is extremely large, and when Cu is added the core loss becomes small and also a proper heat treatment temperature range becomes as high as 540-580C, exceeding that of those containing no Cu. This temperature is higher than the crystallization temperature Tx measured at a temperature-elevating speed of 10 C/minute by DSC.
Incidentally, it was con-Eirmed by transmission electron microscopy that the Fe-base soEt magnetic alloy of the present invention containing Cu was constituted by 50% or more of fine crystalline particles.
Exam~le_22 Amorphous alloy ribbons having the composition of Fe74 5 Cu Mo3Sil3 5Bg ~ere heat-treated under the same conditions as in Example 15, and measured with respect to effective permeability at lkHz. The results are shown in Fig.
13.
As is clear from Fig. 13, those containing no Cu ,, ,: ;.
., ~:
, : : -.. ., , ~, . ::
;,,,: , ~ , ,., , . .. : ~, ~323219 (x=O) have reduced effective permeability ~e under the same heat treatment conditions as in the present invention, while those containing Cu ~present invention) have extremely enhanced effective permeability. The reason therefor is presumably that those containing no Cu (x=O) have large crystalline particles mainly composed of compound phases, while those containing Cu (present invention) have fine a-Fe crystalline particles in which Si and B are dissolved.
Example 23 Amorphous alloy ribbons having the composition of Ye73.5_xCUxSil3.5BgNb3MoO 5V0 5 were heat-treated under the same conditions as in Example 15, and measured with respect to effective permeability at lkHz. The results are shown in Fig.
14.
As is clear from Fig. 14, those containing no Cu (x=O) have reduced effective permeabillty ~e under the same heat treatment conditions as in the present invention, while those containing Cu (present invention) have extremely enhanced effective permeability.
Example 24 Amorphous alloy ribbons having the composition of Fe74 xCuxSil3B8Mo3VlARl were heat-treated under the same conditions as in Example 21, and measured with respect to effective permeability at lkHz. The results are shown in Fig.
15.
As is clear from Fig. 15, those containing no Cu (x=O) have reduced effective permeability ~e under the same heat treatment conditions as in the present invention, while . .,; , ....... -. . .
:. .-.::
132~2:L9 those containing Cu (present invention) have e~tremely enhanced effective permeability.
Example 25 Amorphous alloys having the composition of Fe77 5 x Cu Nb Sil3 5Bg were prepared in the same manner as in Example 1, and measured with respect to crystallization temperature at a temperature-elevating speed of 10 C/minute for various values of x and ~. The results are shown in Fig.
16.
As is clear from Fig. 16, Cu acts to lower the crystallization temperature, while Nb acts to enhance it. The addition of such elements having the opposite tendency in combination appears to ma~e the precipitated crystalline particles finer.
Example 26 Amorphous alloy ribbons having the composition of Fe72 ~CulSil5BgNb3Ru~ were punched in t:he shape for a magnetic head core and then heat-treated at 580"C for one hour. A part of each ribbon was used for observing its microstructure by a transmission electron microscope, and the remaining part of each sample was laminated to form a magnetic head. It was shown that the heat-treated samples consisted substantially of a Eine crystalline particle structure.
Next, each of the resulting magnetic heads was assembled in an automatic reverse cassette tape recorder and subjected to a wear test at temperature of 20C and at humidity of 90%. The tape was turned upside down every 25 hours, and the amount of wear after 100 hours was measured. The results ~52-.. .: . ~ . :
, - . : -' . ,. - :~
. ., ~3232~9 are shown in Eig. 17.
As is clear from Fig. 17, the addition of Ru extremely improves wear resistance, thereby making the alloy more suitable for magnetic heads.
Example 27 Amorphous alloy ribbons of 25~m in thickness and 15mm in width and having the composition of Fe76 5 aCul~baSil3 5Bg t~=3, 5) were prepared by a single roll method. These amorphous alloys were heat-treated at temperatures of 500C or more for one hour. It was observed by an electron microscope that those heat-treated at 500C or higher were 50% or more crystallized.
The heat-treated alloys were measured with respect to Vickers hardness at a load of lOOg. Fig. 18 shows how the Vickers hardness varies depending upon the heat treatment temperature. It is shown that the alloy of the present invention has higher Vickers hardness than the amorphous alloys.
Example 28 Amorphous alloy ribbons having the compositions as shown in Table 7 were prepared and heat-treated, and magnetic heads produced therefrom in the same way as in Example 26 were subjected to a wear test. Table 7 shows wear after 100 hours and corrosion resistance measured by a salt spray test.
The table shows -that the alloys of the present invention containing Ru, Rh, Pd, Os, Ir, Pt, Au, Cr, Ti, V, etc. have better wear resistance and corrosion resistance than those not containing the above elements, and much better than ~ ,, ~ ,, . . . ' : .
: ` : ' ,, ' ,: : ".
"' ' .- ~' , '' '` , " ' ` , ' .~ ' `
,. ' " ' " . . . ' the conventional Co-base amorphous alloy. Further, since the alloy of the present invention can have a saturation magne-tic flux density of lT or more~ it is suitable for magne-tic head materials.
. -54-~ - ~
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i~232:~
Table 7 Sample Alloy Composition Wear Corrosion No. (at %) (~m) Resistance .
1 (FeO 98C0 02)70CUlSil4 9 3 3 2.2 Excellent 70 1 14 9 3 3 ' Excellent 3 Fe69CulSil5BgTa3Ti3 2.1 Good 4 (FeO ggNio 01)70CUlSil4 9 3 3 0.8 Excellent 70 1 15 8 3 3 Excellent 69 1 15 7 5 3 Excellent 7 Fe66 5Cul sSil4Blo 5 3 Excellent 69 1 13 9 5 3 1.0 ~xcellent g Fe71Culsil3BgNb3 3 1.0 Excellent Fe71Culsil3BgNb3 3 2.3 Good 11 Fe70culsil4B9Nb3crlR 2 Excellent 12 Fe68Culsil4BloNb3crlT 1 2 Excellent 13 Fe69CUlSil4B9Nb3TilRU2Rhl 0.4 Excellent 14 Fe7?CulsilsB6Nb3Ru2 1 Excellent Fe73Cul 5Nb3Sil3.5 9 Fair 16 0,94 0.06)75Sil5Blo Amorphous Alloy 10 0 Good Note: No. 16 Conventional alloy . - :, , . :: :, : ~: .
' ~
~3~321~
Example 29 Amorphous alloy ribbons of lOmm in width and 30~m in thickness and having the compositions as shown in Table 8 were prepared by a double-roll method. Each of the amorphous alloy ribbons was punched by a press to form a magnetic head core, -and heat-treated at 550C for one hour and then formed into a magnetic head. It was observed by a transmission electron microscope that the ribbon after the heat treatment was constituted 50% or more by fine crystalline particles of 500 or less.
Part of the heat-treated ribbon was measured with respect to Vickers hardness under a load of lOOg and further a salt spray test was carried out to measure corrosion resistance thereof. The results are shown in Table 8.
Next, the magnetic head was assembled in a cassette tape recorder and a wear test was conducted at temperature of 20C and at humidity of 90~. The amount of wear after lO0 hours are shown in Table 8.
It is clear from the table that the alloy of the present invention has high Vickers hardness and corrosion resistance and further excellent wear resistance, and so are suitable for magnetic head materials, etc.
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~3232:~9 Example 30 Amorphous alloys having the composition of Fe76 5 ~Cu1Nb~Sil3 5Bg were heat--trea-ted at various temperatures for one hour, and the heat-treated alloys were measured with respect to magnetostriction ~s. The results are shown in Table 9.
Table 9 Magnetostriction at_~ach Temperature (xlO ) Nb Content (~) (1) No.tatomic %) _480 500 520550 570 600 650 ~ ~ _ _ _ .
1 3 20.718.6 2.6 8.0 3.8 2.2 _(2) _(2) 15 2 5 13.3_(2) 9.O 7.0 4.0 _(2) 0.6 3.4 Note: (1) Not heat-treated t2) Not measured As is clear from Table 9, the magnetostriction is greatly reduced by the heat treatment of the p:resent invention as :.
compared to the amorphous state. Thus, the alloy of the present invention suffers from less deterioration of magnetic properties caused by magnetostriction than the conventional Fe-base amorphous alloys. Therefore, the Fe-base soft magnetic alloy of the present invention is useful as magnetic head materials.
Example 31 Amorphous alloys having the composition of Fe73_~CUlSil3BgNb3RuO 5C0 5 were heat-treated at various temperatures for one hour, and the heat-treated alloys were , r ;
' . ' . :i' ` ' :
~3232~
measured wlth respect to magne-tostriction ~s. The results are shown in Table 10.
Table 10 Heat Treatment Temperature (C) - 500 550 570 580 ~s(xlO 6)+20.1+2.5 +3.5 -~2.1 +1.8 As is clear from Table 10, the magnetostriction is extremely low when heat-treated according to the present invention than in the amorphous state. Therefore, the Fe-base soft magnetic alloy of the present invention is useful as magnetic head materials. And even with resin im~regnation and coating in the :Eorm of a wound core, it is less likely to be deteriorated in magnetic properties than the wound core of an Fe-base amorphous alloy.
Example 32 Thin amorphous alloy ribbons of 5mm in width and 18~m in thickness and having the compositions as shown in Table 11 were prepared by a single roll method, and each of the ribbons was wound into a toroid of 19mm in outer diameter and 15mm in inner diameter, and then heat-treated at temperatures higher than the crystallization temperature. They were then measured with respect to DC magnetic properties, effective permeability ~elk at lkHz and core loss W2/1ook at lOOkHz and 2kG.
Saturation magnetization ~s was also measured. The results are shown in Table 11~
~32'.321~
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Exal~le 33 Fig. 19 shows the saturation magnetostriction ~s and saturation magnetic flux density Bs of an alloy of Fe73 5CUlNb3siyB22~5-y It is shown that as the Si content (y) increases, the magne-tostriction changes from positive to negative, and that when y is nearly 17 atomic % the magnetostriction is almost 0.
Bs monotonously decreases as the Si content ~y) increases, but its value is about 12KG for a composition which has magnetostriction of 0, higher than that of the Fe-Si-AQ
alloy, etc. by about lKG. Thus, the alloy of the present invention is excellent as magnetic head materials.
Example 34 With respect to a pseudo-ternary alloy of (Fe-Cul-Nb3)-Si-B, its saturation magnetostriction ~s is shown in Fig. 20, its coercive force Hc in F:ig. 21, its effective permeability ~ielK at lkHz in Fig. 22, :its saturation magnetic flux density Bs in Fig. 23 and its core loss W2/1ook at lOOkHz and 2KG in Fig. 24. Fig. 20 shows that in the composition range of the present invention enclosed by the curved line D, the alloy have a low magnetostriction ~s of lOxlO 6 or less.
And in the range enclosed by the curved line E, the alloy have better soft magnetic properties and smaller magnetostriction.
Further, in the composition range enclosed by the curved line F, the alloy has further improved magnetic properties and particularly smaller magnetostriction.
It is shown that when the contents of Si and B are respectively lO<y<25, 3<z<12 and the total of Si and B (y+z) is ~ :, .. : : , . :
:..
. . : , j . .
~32~2~
in the range o~ 18-28, the alloy has a low magnetostriction l~s¦
<5x10 6 and excellent soft magnetic properties.
Particularly when ll<y<24, 3<~<9 and 18<y~z~27, the alloy is highly likely to have a low magnetostriction ¦~s¦
<1.5x10 6. The alloy of the present invention may have magnetostriction of almost 0 and saturation magnetic flux density of 10KG or more. Further, since it has permeability and core loss comparable to those of the Co-base amorphous alloys, the alloy o~ the present invention is highly suitable for various transformers, choke coils, saturable reactors, magnetic heads, etc.
Example 35 A toroidal wound core of l9mm in outer diameter, 15mm in inner diameter and 5mm in height constituted by a 18-~m h s alloY ribbon of Fe73 5CulNb3Sil6.5B6 at various temperatures ~or one hour (temperature-elevating speed: 10 K/minute), air-cooled and then measured with respect to magnetic properties before and a~ter impregration with an epoxy resin. The results are shown in Fig. 25. It also shows the dependency of ~s on heat treatment temperature.
By heat treatment at temperatures higher than the crystallization temperature ~Tx) to make the alloy structure have extremely fine crystalline particlesl the alloy has magnetostriction extremely reduced to almost 0. This in turn minimizes the deterioration of magnetic properties due to resin impregnation. On the other hand, the alloy of the above composition mostly compose of an amorphous phase due to heat treatment at temperatures considerably lower than the - : :
, :''' ' ' , ,i, , , ,,," , "
: :. , .
~'' ',, `
132~2~9 crystallization temperature, for instance, at 470C does not have good magnetic properties even before the resin impregnation, and after the resin impregnation it has extremely increased core loss and coercive force Hc and extremely decreased effective permeability ~elK at lkHz. This is due to a large saturation magnetostriction ~s. Thus, it is clear that as long as the alloy is in an amorphous state, it cannot have sufficient soft magnetic properties after the resin impregnation.
The alloy of the present invention containing fine crystalline particles have small ~s which in turn minimizes the deterioration of magnetic properties 9 and thus its magnetic properties are comparable to those of Co-base amorphous alloys having ~s of almost 0 even after the resin impregnation.
Moreover, since the alloy of the present invention has a high saturation magnetic flux density as shown by magnetic flux density Blo o~ 12KG or so at lOOe, it i5 suitable for magnetic heads, transformers, choke coils, saturable reactors, etc.
Example 36 3~m-thick amorphous alloy layers having the compositions as shown in Table 12 were formed on a crystallized glass ~Photoceram: trade name) substrates by a magnetron sputtering apparatus. Next, each of these layers was heat-treated at temperature higher than the crystallization temperature thereof in an N2 gas atmosphere in a rotational magnetic field of 50000e to provide the alloy layer of the present invention with extremely fine crystalline particles.
Each of them was measured with respect to effective ~ i ` ~ , ,r ;
: : `: '. " ~ . . ,: ., .. ,! . `, .
1~2~2~9 permeability ~elM at lMHz and saturation magnetic flux density Bs. The results are shown in Table 12.
. . .
, , . - . , - .
. . .
~ 32321 ~
Table 12 Sample Composition ~elM Bs (KG) No. (at ~) 1 Fe71 5Cu1 1si15.5B7.0 5.12700 10.7 2 Fe71 7CUo gSil6.5B6.1 4.92700 10.5 3 Fe71 3Cu1 1Sil7.s 5.2 4.92800 10.3 4 Fe74 8Cul oSil2.0B9.lN 3.12400 12.7 Fe71 OCU1 1sil6.oB9.o 2.92500 11.4 6 Fe69 ~Cul oSi1s.o3g.1 5.12400 10.1 7 Fe73 2Cul oSil3 sBg 1 a3 22300 11.4 .
8 Fe71 5CUl.oSi13.6 8.9 5.02200 10~0 g Fe73 2Cul lSil7.5B5.1Nb3.12900 11.9 Fe70 4Cul lSil3.s 12.0 3.02200 11.2 11 Fe78 7Cul oSi8.2B9.1 3.01800 14.5 12 Fe76 gCuo gSil0.2B8~9Nb3~l2000 14.3 13 Fe74 5Nb3Sil7.5 5 Amorphous Alloy50 12.8 14 Co87 ONbs,oZr8.0 Amorphous Alloy2500 12.0 Fe74 7Sil7.9AQ7.4 Alloy 1500 10.3 Note: ~os. 13-15 Conventional alloys - 65 - ;~
.. ..... ~.. " ".... .
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. . . : .
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~323219 Example 37 Amorphous alloy rlbbons of 18~m in thickness and 5mm in width and having the composition of Fe73 5CulNb3Sil3 5B9 were prepared by a single roll method and formed into toroidal wound cores of l9mm in outer diameter and 15mm in inner diameter. These amorphous alloy wound cores were heat-treated at 550C for one hour and then air-cooled. Each of the wound cores thus heat-treated was measured with respect to core loss at lOOkHz to investigate its dependency on Bm. Fig. ~6 shows the dependency of core loss on Bm. For comparison, the dependency of core loss on Bm is shown also for wound cores of P Y ( 68.5 e4.s o2SilsB10), wound cores of an Fe-base amorphous alloy (Fe77CrlSi9B13) and Mn-Zn ferrite.
Fig. 26 shows that the wound cores made of the alloy of the present invention have lower core loss than those of the conventional Fe-base amorphous alloy, the Co-base amorphous alloy and the ferrite. Accordingly, the alloy of the present invention is highly suitable for high-frequency transformers, choke coils, etc.
Example 38 An amorphous alloy ribbon of Fe7oculsil4s9Nb5crl of 15~m in thickness and 5mm in width was prepared by a single roll method and form into a wound core of 19mm in outer diameter and 15mm in inner diameter~ It was then heat-treated by heating at a temperature-elevating speed of 5C/min. while applying a magnetic field of 30000e in perpendicular to the magnetic path of the wound core, keeping it at 620C for one , :..... . ..
: - i . ' : ' . . , :,. , - :
~:
13232~9 hour and then cooling it a-t a speed of 5C/min. to room temperature. Core loss was measured on it. It was confirmed by transmission electron microscopy that the alloy of the present invention had fine crystalline particles. Its direct current B-H curve had a squareness ratio of 8%, which means that it is highly constant in permeability.
For comparison, an Fe-base amorphous alloy (Fe77CrlSigB13), a Co-base amorphous alloy (Co67Fe4Mol 5Sil6 5Bll), and Mn-Zn ferrite were measured with respect to core loss.
Fig. 27 shows the frequency dependency of core loss, in which A denotes the alloy of the present invention, B the Fe-base amorpho~ls alloy, C the Co-base amorphous alloy and D
the Mn-Zn ferrite. As is clear from the figure, the Fe-base lS soft magnetic alloy of the present invention has a core loss which is comparable to that of the conventional Co-base amorphous alloy and much smaller than that of the Fe-base amorphous alloy.
Example 39 An amorphous alloy ribbon of 5mm in width and 15~m in thickness was prepared by a single roll method. The composition of each amorphous alloy was as follows:
Fe73 2CU1Nb3sil3.8 9 Fe73 5CUlM3sil3.5 9 Fe73 5CUlNb3S 13.5 9 Fe71 5CUlNbssil3.5 9 Next, a ribbon of each amorphous alloy was wound to form a toroidal wound core of 15mm in inner diameter and l9mm .~
:: : ,, .;:
in outer diameter. The resulting wound core was heat-treated in a nitrogen atmosphere under the following conditions to provide the alloy of the present invention. It was observed by an electron microscope that each alloy was finely crystallized, 50% or more of which was constituted by fine crystalline particles.
Next, a direct current B-H curve was determined on each alloy. Figs. 28 (a) to (d) show the direct current B-H
curve of each wound core. Fig. 28 (a) shows the direct current B-H curve of a wound core produced from an alloy of the composition of Fe73 2CulNb3Sil3 8Bg (heat treatment conditions:
heated at 550C for one hour and then air-cooled), Fig. 28 (b) the direct current B-H curve of a wound core produced from an alloy of the composition of Fe73 5CulMo3Sil3 5Bg (heat treatment conditions: heated at 530C for one hour and then air-cooled), Fig. 28 (c) the direct current B-H curve of a wound core produced from an alloy of the composition of Fe73 5CulNb3Sil3 5Bg theat treatment conditions: keeping at 550C for one hour, cooling to 280C at a speed of 5C/min.
while applying a magnetic field of lOOe in parallel to the magnetic path oE the wound core, keeping at that temperature for one hour and then air-cooling), and Fig. 28 (d) the direct current B-H curve of a wound core produced from an alloy of the composition of Fe71 5CulNb5Sil3 5Bg (heat treatment conditions:
keeping at 610C for one hour, cooling to 250C at a speed of 10C/min. while applying a magnetic field of lOOe in parallel to the magnetic path of the wound core, keeping at that time for 2 hours and then cir-cooling).
.. . , ;.
, , ,:
:
1~232~
In each graph, the abscissa is Hm (maximum value of the magnetic field) = 100e. Accordingly, in the case of Hm=lOe, 10 is regarded as 1, and in the case of Hm=0.lOe, 10 is regarded as 0.1. In each graph, all of the B-H curves are the same except for difference in the abscissa.
The Fe-base soft magnetic alloy shown in each graph had the following saturation magnetic flux density Blo, coercive force Hc, squareness ratio Br/B10.
Blo(kG) Hc(Oe) / 10( ) Fig. 28 (a) 12.0 0.0088 61 Fig. 28 (b) 12.3 0.011 65 Fig. 28 (c) 12.4 0.0043 93 Fig. 28 (d) 11.4 0.0067 90 In the cases of (a) and (b) heat-treated without applying a magnetic field, the squareness ratio is medium (60%
or so), while in the cases of (c) and (d) heat-treated while applying a magnetic field in parallel to the magnetic path, the squareness ratio is high (90% or more). The coercive force can be 0.010e or less, almost comparable to that of the Co-base amorphous alloy.
In the case of heat treatment without applying a magnetic field, the effective permeability ~e is several tens of thausand to 100,000 at lkHz, suitable for various inductors, sensors, transformers, etc. OII the other hand, in the case of heat treatment while applying a magnetic field in parallel to the magnetic path of the wound core, a high squareness ratio is obtained and also the core loss is 800mW/cc at 100kHz and 2kG, almost comparable to that of Co-base amorphous alloys. Thus, ... . - ; ;. ... .
- . ; ~
, ~. . ; :
-- :, . . ~ :~
; ! . ~ ;
.~ , `
13232~9 it is suitable for saturable reactors, etc.
And some of the alloys of the present invention have a saturation magnetic flux density exceeding lOkG as shown in Fig. 28, which is higher than those of the conventional ~'' ~ ~
~;~ 5 Permalloy and Sendust and general Co-base amorphous alloys.
Thus, the alloy of the present invention can have a large operable magnetic flux density. Therefore, it is advantageous as magnetic materials for magnetic heads, transformers, saturable reactors, chokes, etc.
Also, in thè case of heat treatment in a magnetic field in parallel to the magnetic path, the alloy of the present invention may have a maximum permeability ~m e~ceeding 1,400,000, thus making it suitable for sensors.
Example 40 Two amorphous alloy ribbons of Fe73 5CulNb3Sil3 5Bg and Fe74 5Nb3Sil3 5Bg both having a thickness of 20~m and a width of lOmm were prepared by a single roll method, and X-ray diffraction was meas~tred before and aft:er heat treatment.
Fig. 29 shows X-ray diffraction patterns, in which (a) shows a ribbon of the Fe73 5CulNb3Si13 5Bg alloy before heat treatment, ~b) a ribbon of the Fe73 5CulNb3Sil3 5Bg alloy after heat treatment at 550C for one hour, (c) a ribbon of the Fe7~ 5Nb3Sil3 5Bg alloy after heat treatment at 550C for one hour.
Fig. 29 (a) shows a halo pattern peculiar to an amorphous alloy, which means that the alloy is almost completely in an amorphous state. The alloy of the present invention denoted by (b) shows peaks attributable to crystal ~t~rQ~ mQ(~k~
.
.:- . . . . .
., ~3~3~9 structure, which means that the alloy is almost crystallized.
However, since the crystal particles are fine, the peak has a wide width. On the other hand, with respect to the alloy (c) obtained by heat-treating the amorphous alloy containing no Cu at 550C, it is crystallized but it shows the different pattern from that of (b) containing Cu. It is ~resumed that compounds are precipitated in the alloy (c). The improvement of magnetic properties due to the addition of Cu is presumably due to the fact that the addition of Cu changes the crystallization process which makes it less likely to precipitate compounds and also prevents the crystal particles from becoming coarse.
Example 41 An amorphous alloy ribbon of Fe Cu Si B Nb Cr C of 5mm in width and 15~m in 73.1 1 13.5 9 3 0.2 0.2 thickness was prepared by a single roll method.
Next, each amorphous alloy ribbon was wound to form a toroidal wound core of 19mm in outer cliameter and 15mm in inner diameter. The resulting wound core was heat-treated in a nitrogen atmosphere under the following 3 conditions to prepare the alloy of the present invention. It was confirmed by electron microscopy that it consisted of fine crystalline structure.
Next, the heat-treated wound core was measured with respect to direct current B-H cur~e.
Figs. 30 (a) to (c) show the direct current ~-H curve of the wound core subjected to each heat -treatment.
Specifically, Fig. 30 (a) shows the direc-t current B-H curve of the wound core subjected to -the heat treatment ~ . :
.~ , "
,.
;' `' "' .- ,:, . :
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~3~219 comprising eleva-ting the temperature at a speed of 15C/min. in a nitrogen gas atmosphere, keeping at 550C for one hour and then cooling at a rate of 600C/min. to room temperature, Fig.
30 (b) the dir~ct current B-H curve of the wound core subjected to the heat treatment comprising elevating the temperature from room temperature at a rate of 10C/min. in a netrogen gas atmosphere while applying a DC magnetic field of lOOe in parallel to the magnetic path of the wound core, keeping at 550C for one hour and then cooling to 200C at a rate of 3C/min., and further cooling to room temperature at a rate of 600C/min., and Fig. 30(c) the direct current B-H curve of the wound core subjected to the heat treatment comprising elevating temperature from room temperature at a ra-te of 20C/min. in a nitrogen gas atmosphere while applying a magnetic field of 30000e in perpendicular to the magnetic path of the wound core, keeping at 550C for one hour, and then cooling to 400C at a rate of 3.8C/min. and further cooling to room temperature at a rate of 600C/min.
Fig. 31 shows the frequency dependency of core loss of the above wound cores, in which A denotes a wound core corresponding to Fig. 30 (a), B a wound core corresponding to Fig. 30 (b) and C a wound core corresponding to Fig. 30 (c).
For comparison, the frequency dependency of core loss is also shown for an amorphous wound core D of Co71 5FelMn3CrO 5Sil5Bg having a high squareness ratio (95%), an amorphous wound core E
of Co71 5FelMn3CrO 5Sil5Bg having a low squareness ratio (8%).
As is shown in Fig. 30, the wound core made of the alloy of the present invention can show a direct current B-H
,, ., ;
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~ 3 ~ 9 curve of a high squareness ratio and also a dirrect current B-H
curve of a low squareness ratio and constant permeability, depending upon heat treatment in a magnetic field.
With respect to core loss, the alloy of the present invention shows core loss characteristics comparable to or better than those of the Co-base amorphous alloy wound cores as shown in Fig. 31. The alloy of the present invention has also a high saturation magnetic flux density. Thus, the wound core having a high squareness ratio is highly suitable for saturable reactors used in switching power supplies, preventing spike voltage, magnetic switches, etc., and those having a medium squareness ratio or particularly a low squareness ratio are highly suitable for high-frequency transformers, choke coils, noise filters, etc.
Exarnple 42 An amorphous alloy ribbon of Fe73 5Cu1~b3Si13 5Bg having a thickness of 20~m and a width of lOmm was prepared by a single roll method and heat-treated at 500C for one hour.
The temperature variation of magnetization of the amorphous alloy ribbon was measured by VSM at Hex=800kA/m and at a temperature-elevating speed of lOk/min. For comparison, the temperature variation of magnetization was also measured for those not subjected to heat treatment. The results are shown in Fig. 32 in which the abscissa shows a ratio of the measured magnetization to magnetization at room temperature ~/aR T.
The alloy subjected to the heat treatment of the present invention shows smaller temperature variation of magnetization a than the alloy before the heat treatment which " ~ ", .
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32~219 was almost completely amorphous. This is presumably due to the fact that a main phase occupying most of the alloy structure has higher Curie temperature Tc than the amorphous phase, reducing the temperature dependency of saturation magnetization.
Since the Curie temperature of the main phase is lower than that of pure ~-Fe, it is presumed that the main phase consists of a-Fe in which Si, etc. are dissolved. And Curie temperature tends to increase as the heat treatment temperature increases, showing that the composition of main phase is changeable by heat treatment.
Example 43 An amorphous alloy ribbon of Fe73 5CulNb3Sil3 5Bg having a thickness of 18~m and a width of 4.5mm was prepared by a single roll method and then wound to form a toroidal wound core of 13mm in outer diameter and lOmm in inner diameter.
Next, it was heat-treated in a magnetic field according to various heat treatment patterns as shown in Fig.
33 (magnetic field: in parallel to the magnetic path of the 20 wound core). The measured magnetic properties are shown in Table 13.
Table 13 BloBr/B10 2/lOOk Heat Treatment Condition (T) (%) (mW/cc) (a) 1.2~ 60 320 (b) 1.2~ 90 790 (c) 1.2~ 82 610 ., - : - : ;;
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(d) 1.24 87 820 (e) 1.24 83 680 (f) 1.24 83 680 In the patter (a) in which a magnetic field was applied only in the rapid cooling step, the squareness ratio was not so increased. In other cases, however, the squareness ratio was 80% or more, which means that a high squareness ratio can be achieved by a heat treatment in a magnetic field applied in parallel to the magnetic path of the wound core. The amorphous alloY of Fe73 5CulNb3Sil3.5B9 temperature of about 340C, and the fi~ure of (f) shows that a high squareness ratio can be achieved even by a heat treatment in a mganetic field applied only at temperatures higher than the Curie temperature of the amorphous alloy. The reason therefor is presumeably that the main phase of the finely crystallized alloy of the present invention has Curie temperature higher than the heat treatment temperature.
Incidentally, by a heat treatment in the same pattern in which a magnetic field is applied in perpendicular to the magnetic path of the wound core, the Fe-base soft magnetic alloy can have as low squareness ratio as 30% or less.
As described above in detail, the Fe-base soft magnetic alloy of the present invention contains fine crystalline particles occupying 50% or more of the total alloy structure, so that it has extremely low core loss comparable to that of Co-base amorphous alloys, and also has small time variation of core loss. It has also high permeability and - , : . . , . :. . , ~3232~'~
saturation magnetic flux density and further excellent wear resistance. Further, since it can have low magnetostriction, its magnetic properties are not deteriorated even by resin impregnation and deformation. Because of good higher-frequency magnetic properties, it is highly suitable for high-frequency transformers, choke coils, saturable reactors, magnetic heads, etc.
The present invention has been described by the above Examples, but it should be noted that any modifications can be made unless they deviate from the scope of the present invention defined by the claims attached hereto.
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Example 8 Thin amorphous alloy ribbons of 5mm in width and 18~m in thickness and having the compositions as shown in Table 4 were prepared by a single roll method, and each of the ribbons was wound into a toroid of l9mm in outer diameter and 15mm in inner diameter, and then heat-treated at temperatures higher than the crystallization temperature. They were then measured with respect to DC magnetic properties, effective permeability ~elk at lkHz and core loss 2/lOOk Saturation magnetization ~s was also measured. The results are shown in Table 4.
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~323~9 Table 4 Sample Composition Bs (KG) Hc (Oe) ~elk W2 0 As 6 No. (at ~) (m~CC~ (X10 l Fe74Cu0 sSil3.5B9 3 12.40.01368000 300 +1.8 2 Fe74CU1 5Sil3.5BgN 2 12.6 0.015 76000 230 +2.0 79 1.0 8 9 3 14.60.05621000 470 +1.8 4 Fe74 5Cul oSil3.5 65 11.60.02042000 350 +1.5 Fe77CUl.oSiloB9N 3 14.30.02548000 430 +1.6 6 Fe73 5Cul oSil7.5B53 10.50.01542000 380 -0.3 7 Fe71CU1 5Sil3.5B9 5 11.20.01268000 280 +1.9 8 Fe74Cul oSil4 8 3 12.10.02274000 250 ~1.7 g Fe73Cu2 oSil3.s 8.53 11.60.02829000 350 +2.0 Fe74 5Cul osil3.5B9Ta2 12.80.01833000 480 +1.8 11 Fe72Cul oSil4 8 511.7 0.030 28000 380 +2.0 12 Fe71 5Cul osil3.5B9T 5 11.30.03828000 480 +1.8 13 Fe73Cul 5Sil3.5B9M 3 12.10.01469000 250 +2.8 14 Fe73 5Cul oSil3.5B93 11.4 0.017 43000 330 +1.9 Fe71Cul oSil3 10 5 10.0 0.023 68000 320 +2.5 16 e78 9 13 P 15.6 0.0350003300 +2.7 17 70.3 4.7 15 10 P 8.0 0.006 8500 350 ~ 0 18 Fe84 2sig.6A~6.2 11.0 0.02 10000 - ~ 0 -Note: Nos,16-18 Conventional alloys , . " .; . . i "
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~232~9 Example 9 Each of amorphous alloys having the composition of Fe74 5 xCuxNb3Sil3 5Bg (O<x<3.5) was heat-treated at the following optimum heat treatment temperature for one hour7 and then measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG and a frequency f=lOOkHz.
X (atomic %)Heat Treatment Temperature (C) 10 0.05 500 0.1 520 0.5 540 1.0 550 1.5 550 2.0 540 2.5 ~30 3.0 500 3.2 500 3.5 490 The relations between the content x of Cu (atomic %) and the core loss W2/1ook are shown in Fig. 4. It is clear from Fig. 4 that the core loss decreases as the Cu content x increases from 0, but that when it exceeds about 3 atomic %, the core loss becomes as large as that of alloys containing no Cu. When x is in the range of 0.1-3 atomic %, the core loss is sufficiently small. Particularly desirable range of x appears to be 0.5-2 atomic %.
Example 10 ~3~3219 Each of amorphous alloys having the composition of Fe73_xCUxSil4BgNb3Crl (O<x<3-5) was heat-treated at the following optimum heat treatment temperature for one hour, and then measured with respect to core loss W2/1ook at a wave height of magnetic flux density sm=2kG and a frequency f=lOOkHz.
Heat Treatment Temperature Core Loss X (atomic %) (C) W2/lOOk (mW/cc) o 505 980 0.05 510 900 0.1 520 610 1.0 560 210 1.5 560 230 2.0 550 250 2.5 530 390 3.0 500 630 3.2 500 850 3.5 490 1040 It is clear from the above that the core loss deereases as the Cu eontent x inereases from 0, but that when it exceeds about 3 atomic %, the eore loss becomes as large as that of alloys containing no Cu. When x is in the range of ~ 3 ato~ic %, the core loss is su~iciently small.
Partieularly desirable range of x ap~ears to be 0.5-2 atomie %.
Example 11 Each of amorphous alloys having the composition of Fe69_xCUxSil3.5B9 5Nb5Cr1C2 (O<x<3.5) was heat-treated at the , , ' ' 132~.~2~
following optimum heat treatment temperature for one hour, and then measured with respect to core loss W2/1ook at a wave height of magnetic flux density Bm=2kG and a frequency f=lOOkHz.
Heat Treatment Temperature Core Loss X (atomic %) (C) W2/lOOk (mW/cc) 0.1 535 560 0.5 550 350 1.0 590 240 1.5 580 240 2.0 570 290 2.5 560 440 3.0 550 630 3.2 540 860 It is cLear from the above that the core loss decreases as the Cu content x increase~; from 0, but that when it exceeds about 3 atomic %, the core :Loss becomes as large as that of alloys containing no Cu. When x is in the range of 0.1-3 atomic %, the core loss is sufficiently small.
Particularly desirable range of x appears to be 0.5-2 atomic %.
Example 12 Each of amorphous alloys having the composition of Fe76 5 CulSi13B9 5M' (M'=Nb, W, Ta or Mo) was heat-tr~ated at the following optimum heat treatment temperature for one hour, and then measured with respect to core loss W2/1ook.
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a (atomic %) Heat Treatment Temperature (C) 0.1 405 0.2 410 1.0 430 2.0 ~80 3.0 550 5.0 580 7.0 590 8.0 `590 10.0 590 11.0 590 The results are shown in Fig. 5, in which graphs A, B, C and D show the cases where M' is Nb, W, Ta and Mo, respectively.
As is clear from Fig. 5, the core loss is sufiiciently small when the amount ~ oi.- M' is in the range of 0.1-10 atomic %. And particularly when M' is Nb, the core loss ~`
was extremely low. A particularly des:ired range oE a is 2<~<8.
Example 13 Each of amorphous alloys having the composition of Fe75 5 CulSil3B9 5M'~Til (M'=Nb, W, Ta or Mo) was heat-treated at the following optimum heat treatment temperature for one hour, and then measured with respect to core loss W2/1ook.
a (atomic %)Heat Treatment Temperature (C) 0.1 410 0.2 420 ,,, . ! , ~
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1.0 440 2.0 490 3.0 560 5.0 590 7.0 600 8.0 600 10.0 600 11.0 600 The results are shown in Fig. 6, in which graphs A, B, C and D show the cases where M' is Nb~ W, Ta and Mo, respectively.
As is clear from Fig. 6, the core loss is sufficiently small when the amount a of ~' is in the range of 0.1-10 atomic %. And particularly when M' is Nb, the core loss was extremely low. A particularly desired range of a is 2<a<8.
_xample 14 Each of amorphous alloys havi.ng the composition of Fe75 CulSil3BgNb RulGel was heat-treat:ed at the following optimum heat treatment temperature for one hour, and then 20 measured with respect to core loss W2/1OOk.
a (atomic %)Heat Treatment Temperature (C) 0.1 410 0.2 415 1.0 430 2.0 485 3.0 555 S.0 585 .
, .
- :..
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~323219 7.0 595 8.0 595 10.0 595 11.0 595 The results are shown in Fig. 7. As is clear from Fig. 7, the core loss is sufficiently small when the amount a of Nb is in the range of 0.1-10 atomic %. A particularly desired range of ~ is 2<~<8.
Incidentally, the electron microscopy showed that fine crystalline particles were generated when a was Ool or more.
Example 15 Each oE amorphous alloys having the composition of Fe73.5CulNb3Sil3~9 5 was heat-treated at 550C for one hour.
Their transmission electron microscopy revealed that each of them contained 50% or more of a crystal phase. They were measured with respect to effective permeability ~e at frequency o~ 1 - lxlO"KHz. Similarly? a Co-base amorphous alloy (Co69 6FeO 4Mn6Sil5Bg) and Mn-Zn ferrite were measured with respect to effective permeability ~e. The results are shown in Fig~ 8, in which graphs A, B and C show the heat treated Fe-base soft magnetic alloy of the present invention, the Co-base amorphous alloy and the ferrite, respectively.
Fig. 8 shows that the Fe-base soft magnetic alloy of the present invention has permeability equal to or higher than that of the Co-base amorphous alloy and extremely higher than that of the ferrite in a wide frequency range. Because o~
this, the Fe-base sot magnetic alloy of the present invention .
. ~
~3~32~
is suitable for choke coils, magnetic heads, shielding materials, various sensor materials, etc.
Example 16 Each of amorphous alloys having the composition of Fe72CulSil3 5B9 5Nb3Rul was heat-treated at 550C for one hour.
Their transmission electron microscopy revealed that each of them contained 50% or more of a crystal phase. They were measured with respect to effective permeability ~e at a frequency of 1 - lx104KHz. Similarly a Co-base amorphous alloy (Co69 6FeO 4Mn6Sil5Bg) and Mn-Zn ferrite were measured with respect to effective permeability ~e. The results are shown in Fig. 9, in which graphs A, B and C show the heat-treated Fe-base soft magnetic al].oy of the present invention, the Co-base amorphous alloy and the Eerrite, respectively.
Fig. 9 shows that the Fe-base soft magnetic alloy of the present invention has permeability equal to or higher than that of the Co-base amorphous alloy ancl extremely higher than that of the Eerrite in a wide frequency range.
Example 17 Each of amorphous alloys having the composition o-f Fe71CulSil5B8~b3ZrlPl was heat-treated at 550C for one hour.
Their transmission electron microscopy revealed that each of them contained 50% or more of a crystal phase and then measured with respect to effective permeability ~e at frequency of 1 -lx104KHz. Similarly a Co-base amorphous alloy (co66Fe4~i3Mo2silsBlo)~ an Fe-base amorphous ~lloy (Fe77CrlSil3Bg), and Mn-Zn ferrite were measured with respect to effective permeability ~e. The results are shown in Fig.
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~323219 10, in which graphs A, B, C and D show the heat-treated Fe-base soft magne-tic alloy of the present invention, the Co-base amorphous alloy, the Fe-base amorphous alloy and the ferrite, respectively.
Fig. 10 shows that the Fe-base soft magnetic alloy of the present invention has permeability equal to or higher than that of the Co-base amorphous alloy and extremely higher than that of the Fe-base amorphous alloy and the ferrite in a wide frequency range.
Example 18 Amorphous alloys having the compositions as shown in Table 5 were prepared under the same conditions as in Example 1, and on each alloy the relations between heat treatment conditions and the time variability of core loss were investigated. One heat trea-tment condition was 550C for one hour (according to the present invention), and the other was 400C x 1 hour tconventional method). It was confirmed by electron microscopy that the Fe-base soft magnetic alloy heat-treated at S50C for one hour according to the present invention contained 50% or more of fine crystal phase.
Incidentally, the time variation of core loss (W100-W~)/Wo was calculated from core loss (W0) measured immediately after the heat treatment of the present invention and core loss (W100) measured 100 hours after keeping at 150C, both at 2kG and 100kHz. The results are shown in Table 5.
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, ~23219 Table 5 Time Variation of Core Loss ( Wl o O-WO ) /WO
Alloy Compositlon Heat Treatment of Conventional No. (atomic %) Present Invention Heat Treatment 1 Fe71CUl b3 10 lS
2 Fe70 5Cul sNbsSillB12 3 Fe70 5Cul 5M5Sil3B10 4 Co69Fe4Nb2Sil5B10 1.22 Co69 5Fe4.5M25il5 9 1.30 The above results show that the heat treatment of the present invention reduces the time variation of core loss ~Nos.
1-3). Also it is shown that as compared with the conventional, low-core loss Co-base amorphous alloys (Nos. 4 and 5), the Fe-base soft magnetic alloy of the present invention has extremely reduced time variation of core loss. There~ore, the Fe--base soft magnetic alloy of the present invention can be used Eor highly reliable magnetic parts.
Example 19 Amorphous alloys having the composition as shown in Table 6 were prepared under the same conditions as in Example 1, and on each alloy the relations between heat treatment conditions and Curie t`emperature (Tc) were investigated. One heat treatment condition was 550C x 1 hour (present invention), and the other heat treatment condition was 350~C x 1 hour (conventional method). In the present invention, the Curie temperature was determined from a main phase (fine crystalline particles) occupying most of the alloy structure.
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~3~32~9 It was confirmed by X-ray diffraction that those subjected to heat trea-tment at 350C for 1 hour showed a halo pattern peculiar to amorphous alloys, meaning that they were substantially amorphous. On the other hand, those subjected to heat treatment at 550C for 1 hour showed peaks assigned to crystal phases, showing substantially no halo pattern. Thus, it was confirm that they were substantially composed of crystalline phases. The Curie temperature ~Tc) measured in each heat treatment is shown in Table 6.
Table 6 Curie Temperature (C) Alloy Composition Heat Treatment of Conventional No. (atomic %) Present Invention Heat Treatment 1 Fe73 sCU1Nb3Sil3.5 9 567 340 2 Fe71CU1 5Nb5Sil3.5 9 560 290 3 Fe71 sCUlMsSil3.5 9 560 288 4 Fe74CulTa3sil2Blo 565 334 Fe71 5CUlw5sil3.5 9 561 310 The above results show that the heat treatment of the present invention extremely enhances the Curie temperature (Tc). Thus, the alloy of the present invention has magnetic properties less variable with the temperature change than the amorphous alloys. Such a large difference in Curie temperature between the Fe-base soft magnetic alloy of the present invention and the amorphous alloys is due to the fact that the alloy subjected to the heat treatment of the present lnven-tion /
': .. ~ :
132'321L9 is finely crystallized.
Exampled 20 A ribbon of an amor~hous alloy having the composition of Fe74 5 xCuxNb3Sil3 5~9 (width: 5mm and thickness: 18~m) was formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter and heat-treated at various temperatures for one hour. Core loss W2/1ook at 2kG and lOOkHz was measured on each of them. The results are shown in Fig. 11.
The crystallization temperatures (Tx) of the amorphous alloys used for the wound cores were measured by a differential scanning calorimeter (DSC). The crystallization temperature Tx measured at a temperature-elevating speed of 10 C/minute on each alloy were 583C for x=0 and 507C for x=0.5, 1.0 and 1~5.
As is clear from Fig. 11, when the Cu content x is 0, core loss W2/1ook is extremely large, and as the Cu content increases up to about 1.5 atomic %, the core loss becomes small and also a proper heat treatment temperature range becomes as higher as 540-580C, exceeding that of those containing no Cu.
~his temperature is higher than the crystallization temperature Tx measured at a temperature~elevating speed of 10 C/minute by DSC. Incidentally, it was confirmed by transmission electron microscopy that tlle Fe-base soft magnetic alloy of the present invention containing Cu was constituted by 50% or more of fine crystalline particles.
Example 21 A ribbon of an amorphous alloy having the composition of Fe73 Cu Sil3BgNb3CrlCl (width: 5mm and thickness: 18~m) was .; . .. -. ~.: ::
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~32~2~9 formed into a toroidal wound core of 15mm in inner diameter and l9mm in outer diameter and heat-treated at various temperatures for one hour. Core loss W2/1ook at 2kG and lOOkH~ was measured on each of them. The results are shown in Fig. 12.
The crystallization temperatures (Tx) of the amorphous alloys used for the wound cores were measured by a differential scanning calorimPter ~DSC). The crystallization temperatures Tx measured at a temperature-elevating speed of 10 C/minute on each alloy were 580C for x=0 and 505C for x=0.5, 1.0 and 1.5.
As is clear from Fig. 12, when the Cu content x is 0, core loss W2/1ook is extremely large, and when Cu is added the core loss becomes small and also a proper heat treatment temperature range becomes as high as 540-580C, exceeding that of those containing no Cu. This temperature is higher than the crystallization temperature Tx measured at a temperature-elevating speed of 10 C/minute by DSC.
Incidentally, it was con-Eirmed by transmission electron microscopy that the Fe-base soEt magnetic alloy of the present invention containing Cu was constituted by 50% or more of fine crystalline particles.
Exam~le_22 Amorphous alloy ribbons having the composition of Fe74 5 Cu Mo3Sil3 5Bg ~ere heat-treated under the same conditions as in Example 15, and measured with respect to effective permeability at lkHz. The results are shown in Fig.
13.
As is clear from Fig. 13, those containing no Cu ,, ,: ;.
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;,,,: , ~ , ,., , . .. : ~, ~323219 (x=O) have reduced effective permeability ~e under the same heat treatment conditions as in the present invention, while those containing Cu ~present invention) have extremely enhanced effective permeability. The reason therefor is presumably that those containing no Cu (x=O) have large crystalline particles mainly composed of compound phases, while those containing Cu (present invention) have fine a-Fe crystalline particles in which Si and B are dissolved.
Example 23 Amorphous alloy ribbons having the composition of Ye73.5_xCUxSil3.5BgNb3MoO 5V0 5 were heat-treated under the same conditions as in Example 15, and measured with respect to effective permeability at lkHz. The results are shown in Fig.
14.
As is clear from Fig. 14, those containing no Cu (x=O) have reduced effective permeabillty ~e under the same heat treatment conditions as in the present invention, while those containing Cu (present invention) have extremely enhanced effective permeability.
Example 24 Amorphous alloy ribbons having the composition of Fe74 xCuxSil3B8Mo3VlARl were heat-treated under the same conditions as in Example 21, and measured with respect to effective permeability at lkHz. The results are shown in Fig.
15.
As is clear from Fig. 15, those containing no Cu (x=O) have reduced effective permeability ~e under the same heat treatment conditions as in the present invention, while . .,; , ....... -. . .
:. .-.::
132~2:L9 those containing Cu (present invention) have e~tremely enhanced effective permeability.
Example 25 Amorphous alloys having the composition of Fe77 5 x Cu Nb Sil3 5Bg were prepared in the same manner as in Example 1, and measured with respect to crystallization temperature at a temperature-elevating speed of 10 C/minute for various values of x and ~. The results are shown in Fig.
16.
As is clear from Fig. 16, Cu acts to lower the crystallization temperature, while Nb acts to enhance it. The addition of such elements having the opposite tendency in combination appears to ma~e the precipitated crystalline particles finer.
Example 26 Amorphous alloy ribbons having the composition of Fe72 ~CulSil5BgNb3Ru~ were punched in t:he shape for a magnetic head core and then heat-treated at 580"C for one hour. A part of each ribbon was used for observing its microstructure by a transmission electron microscope, and the remaining part of each sample was laminated to form a magnetic head. It was shown that the heat-treated samples consisted substantially of a Eine crystalline particle structure.
Next, each of the resulting magnetic heads was assembled in an automatic reverse cassette tape recorder and subjected to a wear test at temperature of 20C and at humidity of 90%. The tape was turned upside down every 25 hours, and the amount of wear after 100 hours was measured. The results ~52-.. .: . ~ . :
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. ., ~3232~9 are shown in Eig. 17.
As is clear from Fig. 17, the addition of Ru extremely improves wear resistance, thereby making the alloy more suitable for magnetic heads.
Example 27 Amorphous alloy ribbons of 25~m in thickness and 15mm in width and having the composition of Fe76 5 aCul~baSil3 5Bg t~=3, 5) were prepared by a single roll method. These amorphous alloys were heat-treated at temperatures of 500C or more for one hour. It was observed by an electron microscope that those heat-treated at 500C or higher were 50% or more crystallized.
The heat-treated alloys were measured with respect to Vickers hardness at a load of lOOg. Fig. 18 shows how the Vickers hardness varies depending upon the heat treatment temperature. It is shown that the alloy of the present invention has higher Vickers hardness than the amorphous alloys.
Example 28 Amorphous alloy ribbons having the compositions as shown in Table 7 were prepared and heat-treated, and magnetic heads produced therefrom in the same way as in Example 26 were subjected to a wear test. Table 7 shows wear after 100 hours and corrosion resistance measured by a salt spray test.
The table shows -that the alloys of the present invention containing Ru, Rh, Pd, Os, Ir, Pt, Au, Cr, Ti, V, etc. have better wear resistance and corrosion resistance than those not containing the above elements, and much better than ~ ,, ~ ,, . . . ' : .
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Table 7 Sample Alloy Composition Wear Corrosion No. (at %) (~m) Resistance .
1 (FeO 98C0 02)70CUlSil4 9 3 3 2.2 Excellent 70 1 14 9 3 3 ' Excellent 3 Fe69CulSil5BgTa3Ti3 2.1 Good 4 (FeO ggNio 01)70CUlSil4 9 3 3 0.8 Excellent 70 1 15 8 3 3 Excellent 69 1 15 7 5 3 Excellent 7 Fe66 5Cul sSil4Blo 5 3 Excellent 69 1 13 9 5 3 1.0 ~xcellent g Fe71Culsil3BgNb3 3 1.0 Excellent Fe71Culsil3BgNb3 3 2.3 Good 11 Fe70culsil4B9Nb3crlR 2 Excellent 12 Fe68Culsil4BloNb3crlT 1 2 Excellent 13 Fe69CUlSil4B9Nb3TilRU2Rhl 0.4 Excellent 14 Fe7?CulsilsB6Nb3Ru2 1 Excellent Fe73Cul 5Nb3Sil3.5 9 Fair 16 0,94 0.06)75Sil5Blo Amorphous Alloy 10 0 Good Note: No. 16 Conventional alloy . - :, , . :: :, : ~: .
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Example 29 Amorphous alloy ribbons of lOmm in width and 30~m in thickness and having the compositions as shown in Table 8 were prepared by a double-roll method. Each of the amorphous alloy ribbons was punched by a press to form a magnetic head core, -and heat-treated at 550C for one hour and then formed into a magnetic head. It was observed by a transmission electron microscope that the ribbon after the heat treatment was constituted 50% or more by fine crystalline particles of 500 or less.
Part of the heat-treated ribbon was measured with respect to Vickers hardness under a load of lOOg and further a salt spray test was carried out to measure corrosion resistance thereof. The results are shown in Table 8.
Next, the magnetic head was assembled in a cassette tape recorder and a wear test was conducted at temperature of 20C and at humidity of 90~. The amount of wear after lO0 hours are shown in Table 8.
It is clear from the table that the alloy of the present invention has high Vickers hardness and corrosion resistance and further excellent wear resistance, and so are suitable for magnetic head materials, etc.
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~3232:~9 Example 30 Amorphous alloys having the composition of Fe76 5 ~Cu1Nb~Sil3 5Bg were heat--trea-ted at various temperatures for one hour, and the heat-treated alloys were measured with respect to magnetostriction ~s. The results are shown in Table 9.
Table 9 Magnetostriction at_~ach Temperature (xlO ) Nb Content (~) (1) No.tatomic %) _480 500 520550 570 600 650 ~ ~ _ _ _ .
1 3 20.718.6 2.6 8.0 3.8 2.2 _(2) _(2) 15 2 5 13.3_(2) 9.O 7.0 4.0 _(2) 0.6 3.4 Note: (1) Not heat-treated t2) Not measured As is clear from Table 9, the magnetostriction is greatly reduced by the heat treatment of the p:resent invention as :.
compared to the amorphous state. Thus, the alloy of the present invention suffers from less deterioration of magnetic properties caused by magnetostriction than the conventional Fe-base amorphous alloys. Therefore, the Fe-base soft magnetic alloy of the present invention is useful as magnetic head materials.
Example 31 Amorphous alloys having the composition of Fe73_~CUlSil3BgNb3RuO 5C0 5 were heat-treated at various temperatures for one hour, and the heat-treated alloys were , r ;
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~3232~
measured wlth respect to magne-tostriction ~s. The results are shown in Table 10.
Table 10 Heat Treatment Temperature (C) - 500 550 570 580 ~s(xlO 6)+20.1+2.5 +3.5 -~2.1 +1.8 As is clear from Table 10, the magnetostriction is extremely low when heat-treated according to the present invention than in the amorphous state. Therefore, the Fe-base soft magnetic alloy of the present invention is useful as magnetic head materials. And even with resin im~regnation and coating in the :Eorm of a wound core, it is less likely to be deteriorated in magnetic properties than the wound core of an Fe-base amorphous alloy.
Example 32 Thin amorphous alloy ribbons of 5mm in width and 18~m in thickness and having the compositions as shown in Table 11 were prepared by a single roll method, and each of the ribbons was wound into a toroid of 19mm in outer diameter and 15mm in inner diameter, and then heat-treated at temperatures higher than the crystallization temperature. They were then measured with respect to DC magnetic properties, effective permeability ~elk at lkHz and core loss W2/1ook at lOOkHz and 2kG.
Saturation magnetization ~s was also measured. The results are shown in Table 11~
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Exal~le 33 Fig. 19 shows the saturation magnetostriction ~s and saturation magnetic flux density Bs of an alloy of Fe73 5CUlNb3siyB22~5-y It is shown that as the Si content (y) increases, the magne-tostriction changes from positive to negative, and that when y is nearly 17 atomic % the magnetostriction is almost 0.
Bs monotonously decreases as the Si content ~y) increases, but its value is about 12KG for a composition which has magnetostriction of 0, higher than that of the Fe-Si-AQ
alloy, etc. by about lKG. Thus, the alloy of the present invention is excellent as magnetic head materials.
Example 34 With respect to a pseudo-ternary alloy of (Fe-Cul-Nb3)-Si-B, its saturation magnetostriction ~s is shown in Fig. 20, its coercive force Hc in F:ig. 21, its effective permeability ~ielK at lkHz in Fig. 22, :its saturation magnetic flux density Bs in Fig. 23 and its core loss W2/1ook at lOOkHz and 2KG in Fig. 24. Fig. 20 shows that in the composition range of the present invention enclosed by the curved line D, the alloy have a low magnetostriction ~s of lOxlO 6 or less.
And in the range enclosed by the curved line E, the alloy have better soft magnetic properties and smaller magnetostriction.
Further, in the composition range enclosed by the curved line F, the alloy has further improved magnetic properties and particularly smaller magnetostriction.
It is shown that when the contents of Si and B are respectively lO<y<25, 3<z<12 and the total of Si and B (y+z) is ~ :, .. : : , . :
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~32~2~
in the range o~ 18-28, the alloy has a low magnetostriction l~s¦
<5x10 6 and excellent soft magnetic properties.
Particularly when ll<y<24, 3<~<9 and 18<y~z~27, the alloy is highly likely to have a low magnetostriction ¦~s¦
<1.5x10 6. The alloy of the present invention may have magnetostriction of almost 0 and saturation magnetic flux density of 10KG or more. Further, since it has permeability and core loss comparable to those of the Co-base amorphous alloys, the alloy o~ the present invention is highly suitable for various transformers, choke coils, saturable reactors, magnetic heads, etc.
Example 35 A toroidal wound core of l9mm in outer diameter, 15mm in inner diameter and 5mm in height constituted by a 18-~m h s alloY ribbon of Fe73 5CulNb3Sil6.5B6 at various temperatures ~or one hour (temperature-elevating speed: 10 K/minute), air-cooled and then measured with respect to magnetic properties before and a~ter impregration with an epoxy resin. The results are shown in Fig. 25. It also shows the dependency of ~s on heat treatment temperature.
By heat treatment at temperatures higher than the crystallization temperature ~Tx) to make the alloy structure have extremely fine crystalline particlesl the alloy has magnetostriction extremely reduced to almost 0. This in turn minimizes the deterioration of magnetic properties due to resin impregnation. On the other hand, the alloy of the above composition mostly compose of an amorphous phase due to heat treatment at temperatures considerably lower than the - : :
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132~2~9 crystallization temperature, for instance, at 470C does not have good magnetic properties even before the resin impregnation, and after the resin impregnation it has extremely increased core loss and coercive force Hc and extremely decreased effective permeability ~elK at lkHz. This is due to a large saturation magnetostriction ~s. Thus, it is clear that as long as the alloy is in an amorphous state, it cannot have sufficient soft magnetic properties after the resin impregnation.
The alloy of the present invention containing fine crystalline particles have small ~s which in turn minimizes the deterioration of magnetic properties 9 and thus its magnetic properties are comparable to those of Co-base amorphous alloys having ~s of almost 0 even after the resin impregnation.
Moreover, since the alloy of the present invention has a high saturation magnetic flux density as shown by magnetic flux density Blo o~ 12KG or so at lOOe, it i5 suitable for magnetic heads, transformers, choke coils, saturable reactors, etc.
Example 36 3~m-thick amorphous alloy layers having the compositions as shown in Table 12 were formed on a crystallized glass ~Photoceram: trade name) substrates by a magnetron sputtering apparatus. Next, each of these layers was heat-treated at temperature higher than the crystallization temperature thereof in an N2 gas atmosphere in a rotational magnetic field of 50000e to provide the alloy layer of the present invention with extremely fine crystalline particles.
Each of them was measured with respect to effective ~ i ` ~ , ,r ;
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1~2~2~9 permeability ~elM at lMHz and saturation magnetic flux density Bs. The results are shown in Table 12.
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Table 12 Sample Composition ~elM Bs (KG) No. (at ~) 1 Fe71 5Cu1 1si15.5B7.0 5.12700 10.7 2 Fe71 7CUo gSil6.5B6.1 4.92700 10.5 3 Fe71 3Cu1 1Sil7.s 5.2 4.92800 10.3 4 Fe74 8Cul oSil2.0B9.lN 3.12400 12.7 Fe71 OCU1 1sil6.oB9.o 2.92500 11.4 6 Fe69 ~Cul oSi1s.o3g.1 5.12400 10.1 7 Fe73 2Cul oSil3 sBg 1 a3 22300 11.4 .
8 Fe71 5CUl.oSi13.6 8.9 5.02200 10~0 g Fe73 2Cul lSil7.5B5.1Nb3.12900 11.9 Fe70 4Cul lSil3.s 12.0 3.02200 11.2 11 Fe78 7Cul oSi8.2B9.1 3.01800 14.5 12 Fe76 gCuo gSil0.2B8~9Nb3~l2000 14.3 13 Fe74 5Nb3Sil7.5 5 Amorphous Alloy50 12.8 14 Co87 ONbs,oZr8.0 Amorphous Alloy2500 12.0 Fe74 7Sil7.9AQ7.4 Alloy 1500 10.3 Note: ~os. 13-15 Conventional alloys - 65 - ;~
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~323219 Example 37 Amorphous alloy rlbbons of 18~m in thickness and 5mm in width and having the composition of Fe73 5CulNb3Sil3 5B9 were prepared by a single roll method and formed into toroidal wound cores of l9mm in outer diameter and 15mm in inner diameter. These amorphous alloy wound cores were heat-treated at 550C for one hour and then air-cooled. Each of the wound cores thus heat-treated was measured with respect to core loss at lOOkHz to investigate its dependency on Bm. Fig. ~6 shows the dependency of core loss on Bm. For comparison, the dependency of core loss on Bm is shown also for wound cores of P Y ( 68.5 e4.s o2SilsB10), wound cores of an Fe-base amorphous alloy (Fe77CrlSi9B13) and Mn-Zn ferrite.
Fig. 26 shows that the wound cores made of the alloy of the present invention have lower core loss than those of the conventional Fe-base amorphous alloy, the Co-base amorphous alloy and the ferrite. Accordingly, the alloy of the present invention is highly suitable for high-frequency transformers, choke coils, etc.
Example 38 An amorphous alloy ribbon of Fe7oculsil4s9Nb5crl of 15~m in thickness and 5mm in width was prepared by a single roll method and form into a wound core of 19mm in outer diameter and 15mm in inner diameter~ It was then heat-treated by heating at a temperature-elevating speed of 5C/min. while applying a magnetic field of 30000e in perpendicular to the magnetic path of the wound core, keeping it at 620C for one , :..... . ..
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13232~9 hour and then cooling it a-t a speed of 5C/min. to room temperature. Core loss was measured on it. It was confirmed by transmission electron microscopy that the alloy of the present invention had fine crystalline particles. Its direct current B-H curve had a squareness ratio of 8%, which means that it is highly constant in permeability.
For comparison, an Fe-base amorphous alloy (Fe77CrlSigB13), a Co-base amorphous alloy (Co67Fe4Mol 5Sil6 5Bll), and Mn-Zn ferrite were measured with respect to core loss.
Fig. 27 shows the frequency dependency of core loss, in which A denotes the alloy of the present invention, B the Fe-base amorpho~ls alloy, C the Co-base amorphous alloy and D
the Mn-Zn ferrite. As is clear from the figure, the Fe-base lS soft magnetic alloy of the present invention has a core loss which is comparable to that of the conventional Co-base amorphous alloy and much smaller than that of the Fe-base amorphous alloy.
Example 39 An amorphous alloy ribbon of 5mm in width and 15~m in thickness was prepared by a single roll method. The composition of each amorphous alloy was as follows:
Fe73 2CU1Nb3sil3.8 9 Fe73 5CUlM3sil3.5 9 Fe73 5CUlNb3S 13.5 9 Fe71 5CUlNbssil3.5 9 Next, a ribbon of each amorphous alloy was wound to form a toroidal wound core of 15mm in inner diameter and l9mm .~
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in outer diameter. The resulting wound core was heat-treated in a nitrogen atmosphere under the following conditions to provide the alloy of the present invention. It was observed by an electron microscope that each alloy was finely crystallized, 50% or more of which was constituted by fine crystalline particles.
Next, a direct current B-H curve was determined on each alloy. Figs. 28 (a) to (d) show the direct current B-H
curve of each wound core. Fig. 28 (a) shows the direct current B-H curve of a wound core produced from an alloy of the composition of Fe73 2CulNb3Sil3 8Bg (heat treatment conditions:
heated at 550C for one hour and then air-cooled), Fig. 28 (b) the direct current B-H curve of a wound core produced from an alloy of the composition of Fe73 5CulMo3Sil3 5Bg (heat treatment conditions: heated at 530C for one hour and then air-cooled), Fig. 28 (c) the direct current B-H curve of a wound core produced from an alloy of the composition of Fe73 5CulNb3Sil3 5Bg theat treatment conditions: keeping at 550C for one hour, cooling to 280C at a speed of 5C/min.
while applying a magnetic field of lOOe in parallel to the magnetic path oE the wound core, keeping at that temperature for one hour and then air-cooling), and Fig. 28 (d) the direct current B-H curve of a wound core produced from an alloy of the composition of Fe71 5CulNb5Sil3 5Bg (heat treatment conditions:
keeping at 610C for one hour, cooling to 250C at a speed of 10C/min. while applying a magnetic field of lOOe in parallel to the magnetic path of the wound core, keeping at that time for 2 hours and then cir-cooling).
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In each graph, the abscissa is Hm (maximum value of the magnetic field) = 100e. Accordingly, in the case of Hm=lOe, 10 is regarded as 1, and in the case of Hm=0.lOe, 10 is regarded as 0.1. In each graph, all of the B-H curves are the same except for difference in the abscissa.
The Fe-base soft magnetic alloy shown in each graph had the following saturation magnetic flux density Blo, coercive force Hc, squareness ratio Br/B10.
Blo(kG) Hc(Oe) / 10( ) Fig. 28 (a) 12.0 0.0088 61 Fig. 28 (b) 12.3 0.011 65 Fig. 28 (c) 12.4 0.0043 93 Fig. 28 (d) 11.4 0.0067 90 In the cases of (a) and (b) heat-treated without applying a magnetic field, the squareness ratio is medium (60%
or so), while in the cases of (c) and (d) heat-treated while applying a magnetic field in parallel to the magnetic path, the squareness ratio is high (90% or more). The coercive force can be 0.010e or less, almost comparable to that of the Co-base amorphous alloy.
In the case of heat treatment without applying a magnetic field, the effective permeability ~e is several tens of thausand to 100,000 at lkHz, suitable for various inductors, sensors, transformers, etc. OII the other hand, in the case of heat treatment while applying a magnetic field in parallel to the magnetic path of the wound core, a high squareness ratio is obtained and also the core loss is 800mW/cc at 100kHz and 2kG, almost comparable to that of Co-base amorphous alloys. Thus, ... . - ; ;. ... .
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13232~9 it is suitable for saturable reactors, etc.
And some of the alloys of the present invention have a saturation magnetic flux density exceeding lOkG as shown in Fig. 28, which is higher than those of the conventional ~'' ~ ~
~;~ 5 Permalloy and Sendust and general Co-base amorphous alloys.
Thus, the alloy of the present invention can have a large operable magnetic flux density. Therefore, it is advantageous as magnetic materials for magnetic heads, transformers, saturable reactors, chokes, etc.
Also, in thè case of heat treatment in a magnetic field in parallel to the magnetic path, the alloy of the present invention may have a maximum permeability ~m e~ceeding 1,400,000, thus making it suitable for sensors.
Example 40 Two amorphous alloy ribbons of Fe73 5CulNb3Sil3 5Bg and Fe74 5Nb3Sil3 5Bg both having a thickness of 20~m and a width of lOmm were prepared by a single roll method, and X-ray diffraction was meas~tred before and aft:er heat treatment.
Fig. 29 shows X-ray diffraction patterns, in which (a) shows a ribbon of the Fe73 5CulNb3Si13 5Bg alloy before heat treatment, ~b) a ribbon of the Fe73 5CulNb3Sil3 5Bg alloy after heat treatment at 550C for one hour, (c) a ribbon of the Fe7~ 5Nb3Sil3 5Bg alloy after heat treatment at 550C for one hour.
Fig. 29 (a) shows a halo pattern peculiar to an amorphous alloy, which means that the alloy is almost completely in an amorphous state. The alloy of the present invention denoted by (b) shows peaks attributable to crystal ~t~rQ~ mQ(~k~
.
.:- . . . . .
., ~3~3~9 structure, which means that the alloy is almost crystallized.
However, since the crystal particles are fine, the peak has a wide width. On the other hand, with respect to the alloy (c) obtained by heat-treating the amorphous alloy containing no Cu at 550C, it is crystallized but it shows the different pattern from that of (b) containing Cu. It is ~resumed that compounds are precipitated in the alloy (c). The improvement of magnetic properties due to the addition of Cu is presumably due to the fact that the addition of Cu changes the crystallization process which makes it less likely to precipitate compounds and also prevents the crystal particles from becoming coarse.
Example 41 An amorphous alloy ribbon of Fe Cu Si B Nb Cr C of 5mm in width and 15~m in 73.1 1 13.5 9 3 0.2 0.2 thickness was prepared by a single roll method.
Next, each amorphous alloy ribbon was wound to form a toroidal wound core of 19mm in outer cliameter and 15mm in inner diameter. The resulting wound core was heat-treated in a nitrogen atmosphere under the following 3 conditions to prepare the alloy of the present invention. It was confirmed by electron microscopy that it consisted of fine crystalline structure.
Next, the heat-treated wound core was measured with respect to direct current B-H cur~e.
Figs. 30 (a) to (c) show the direct current ~-H curve of the wound core subjected to each heat -treatment.
Specifically, Fig. 30 (a) shows the direc-t current B-H curve of the wound core subjected to -the heat treatment ~ . :
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~3~219 comprising eleva-ting the temperature at a speed of 15C/min. in a nitrogen gas atmosphere, keeping at 550C for one hour and then cooling at a rate of 600C/min. to room temperature, Fig.
30 (b) the dir~ct current B-H curve of the wound core subjected to the heat treatment comprising elevating the temperature from room temperature at a rate of 10C/min. in a netrogen gas atmosphere while applying a DC magnetic field of lOOe in parallel to the magnetic path of the wound core, keeping at 550C for one hour and then cooling to 200C at a rate of 3C/min., and further cooling to room temperature at a rate of 600C/min., and Fig. 30(c) the direct current B-H curve of the wound core subjected to the heat treatment comprising elevating temperature from room temperature at a ra-te of 20C/min. in a nitrogen gas atmosphere while applying a magnetic field of 30000e in perpendicular to the magnetic path of the wound core, keeping at 550C for one hour, and then cooling to 400C at a rate of 3.8C/min. and further cooling to room temperature at a rate of 600C/min.
Fig. 31 shows the frequency dependency of core loss of the above wound cores, in which A denotes a wound core corresponding to Fig. 30 (a), B a wound core corresponding to Fig. 30 (b) and C a wound core corresponding to Fig. 30 (c).
For comparison, the frequency dependency of core loss is also shown for an amorphous wound core D of Co71 5FelMn3CrO 5Sil5Bg having a high squareness ratio (95%), an amorphous wound core E
of Co71 5FelMn3CrO 5Sil5Bg having a low squareness ratio (8%).
As is shown in Fig. 30, the wound core made of the alloy of the present invention can show a direct current B-H
,, ., ;
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: : .
~ 3 ~ 9 curve of a high squareness ratio and also a dirrect current B-H
curve of a low squareness ratio and constant permeability, depending upon heat treatment in a magnetic field.
With respect to core loss, the alloy of the present invention shows core loss characteristics comparable to or better than those of the Co-base amorphous alloy wound cores as shown in Fig. 31. The alloy of the present invention has also a high saturation magnetic flux density. Thus, the wound core having a high squareness ratio is highly suitable for saturable reactors used in switching power supplies, preventing spike voltage, magnetic switches, etc., and those having a medium squareness ratio or particularly a low squareness ratio are highly suitable for high-frequency transformers, choke coils, noise filters, etc.
Exarnple 42 An amorphous alloy ribbon of Fe73 5Cu1~b3Si13 5Bg having a thickness of 20~m and a width of lOmm was prepared by a single roll method and heat-treated at 500C for one hour.
The temperature variation of magnetization of the amorphous alloy ribbon was measured by VSM at Hex=800kA/m and at a temperature-elevating speed of lOk/min. For comparison, the temperature variation of magnetization was also measured for those not subjected to heat treatment. The results are shown in Fig. 32 in which the abscissa shows a ratio of the measured magnetization to magnetization at room temperature ~/aR T.
The alloy subjected to the heat treatment of the present invention shows smaller temperature variation of magnetization a than the alloy before the heat treatment which " ~ ", .
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32~219 was almost completely amorphous. This is presumably due to the fact that a main phase occupying most of the alloy structure has higher Curie temperature Tc than the amorphous phase, reducing the temperature dependency of saturation magnetization.
Since the Curie temperature of the main phase is lower than that of pure ~-Fe, it is presumed that the main phase consists of a-Fe in which Si, etc. are dissolved. And Curie temperature tends to increase as the heat treatment temperature increases, showing that the composition of main phase is changeable by heat treatment.
Example 43 An amorphous alloy ribbon of Fe73 5CulNb3Sil3 5Bg having a thickness of 18~m and a width of 4.5mm was prepared by a single roll method and then wound to form a toroidal wound core of 13mm in outer diameter and lOmm in inner diameter.
Next, it was heat-treated in a magnetic field according to various heat treatment patterns as shown in Fig.
33 (magnetic field: in parallel to the magnetic path of the 20 wound core). The measured magnetic properties are shown in Table 13.
Table 13 BloBr/B10 2/lOOk Heat Treatment Condition (T) (%) (mW/cc) (a) 1.2~ 60 320 (b) 1.2~ 90 790 (c) 1.2~ 82 610 ., - : - : ;;
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(d) 1.24 87 820 (e) 1.24 83 680 (f) 1.24 83 680 In the patter (a) in which a magnetic field was applied only in the rapid cooling step, the squareness ratio was not so increased. In other cases, however, the squareness ratio was 80% or more, which means that a high squareness ratio can be achieved by a heat treatment in a magnetic field applied in parallel to the magnetic path of the wound core. The amorphous alloY of Fe73 5CulNb3Sil3.5B9 temperature of about 340C, and the fi~ure of (f) shows that a high squareness ratio can be achieved even by a heat treatment in a mganetic field applied only at temperatures higher than the Curie temperature of the amorphous alloy. The reason therefor is presumeably that the main phase of the finely crystallized alloy of the present invention has Curie temperature higher than the heat treatment temperature.
Incidentally, by a heat treatment in the same pattern in which a magnetic field is applied in perpendicular to the magnetic path of the wound core, the Fe-base soft magnetic alloy can have as low squareness ratio as 30% or less.
As described above in detail, the Fe-base soft magnetic alloy of the present invention contains fine crystalline particles occupying 50% or more of the total alloy structure, so that it has extremely low core loss comparable to that of Co-base amorphous alloys, and also has small time variation of core loss. It has also high permeability and - , : . . , . :. . , ~3232~'~
saturation magnetic flux density and further excellent wear resistance. Further, since it can have low magnetostriction, its magnetic properties are not deteriorated even by resin impregnation and deformation. Because of good higher-frequency magnetic properties, it is highly suitable for high-frequency transformers, choke coils, saturable reactors, magnetic heads, etc.
The present invention has been described by the above Examples, but it should be noted that any modifications can be made unless they deviate from the scope of the present invention defined by the claims attached hereto.
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Claims (35)
1. An Fe-base soft magne-tic alloy having the composition represented by the general formula:
(Fe1-aMa)100-x-y-z-.alpha.CuxsiyBzM'.alpha.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, and a, x, y, z and a respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30 and 0.1?.alpha.?30, at least 50% of the alloy structure being occupied by fine crystalline particles.
(Fe1-aMa)100-x-y-z-.alpha.CuxsiyBzM'.alpha.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, and a, x, y, z and a respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30 and 0.1?.alpha.?30, at least 50% of the alloy structure being occupied by fine crystalline particles.
2. The Fe-base soft magnetic alloy according to claim 1, wherein the balance of said alloy structure is substantially amorphous, and said crystalline particles have an average particle size of 1000.ANG. or less.
3. The Fe-base soft magnetic alloy according to claim 1, wherein said alloy structure is substantially composed of said fine crystalline particles.
4. The Fe-base soft magnetic alloy according to claim 1, wherein said a, x, y, z and .alpha. respectively satisfy 0?a?0.1, 0.1?x?3, 6?y?25, 2?z?25, 14?y+z?30 and 0.1?.alpha.?10, and at least 50% of the alloy structure consists of fine crystalline particles having an average particle size of 1000.ANG. or less when measured on their maximum sizes, thus having low magnetostriction.
5. The Fe-base soft magnetic alloy according to claim 1, wherein said a, x, y, z and .alpha. respectively satisfy 0?a?0.1, 0.5?x?2, 10?y?25, 3?z?18, 18?y+z?28 and 2?.alpha.?8.
6. The Fe-base soft magnetic alloy having a low magnetostriction according to claim 5, wherein said a, x, y, z and .alpha. respectively satisfy 0?a?0.05, 0.5?x?2, 11?y?24, 3?z?9, 18?y+z?27 and 2?.alpha.?8.
7. The Fe-base soft magnetic alloy having a low magnetostriction according to claim 5, wherein said M' is Nb.
8. The Fe-base soft magnetic alloy according to claim 5, wherein the balance of said alloy structure is substantially amorphous.
9. The Fe-base soft magnetic alloy having a low magnetostriction according to claim 5, wherein said alloy structure substantially consists of fine crystalline particles.
10. The Fe-base soft magnetic alloy according to any one of claims 1-9, wherein said fine crystalline particles have an average particle size of 500.ANG. or less.
11. The Fe-base soft magnetic alloy according to claim 10, wherein said fine crystalline particles have an average particle size of 200.ANG. or less.
12. The Fe-base soft magnetic alloy having a low magnetostriction according to claim 10, wherein said crystalline particles have an average particle size of 50-200.ANG..
13. The Fe-base soft magnetic alloy having a low magnetostriction according to claim 5, wherein said crystalline particles are mainly composed of an iron solid solution having a bcc structure.
14. The Fe-base soft magnetic alloy having a low magnetostriction according to claim 5, having a saturation magnetostriction .lambda.s between -5x10-6 and +5x10-6.
15. The Fe-base soft magnetic alloy according to claim 14, wherein said saturation magnetostriction .lambda.s is in the range of -1.5x10-6 - +1.5x10-6.
16. A method of producing an Fe-base soft magnetic alloy having the composition represented by the general formula:
(Fe1-aMa)100-x-y-z-.alpha.CuxSiyBzM'.alpha.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, and a, x, y, z and a respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30 and 0.1?.alpha.?30, at least 50% of the alloy structure being occupied by fine crystalline particles, comprising the steps of:
(a) rapidly quenching a melt of the above composition to provide an amorphous alloy; and (b) heat-treating said amorphous alloy to generate fine crystalline particles therein.
(Fe1-aMa)100-x-y-z-.alpha.CuxSiyBzM'.alpha.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, and a, x, y, z and a respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30 and 0.1?.alpha.?30, at least 50% of the alloy structure being occupied by fine crystalline particles, comprising the steps of:
(a) rapidly quenching a melt of the above composition to provide an amorphous alloy; and (b) heat-treating said amorphous alloy to generate fine crystalline particles therein.
17. The method of according to claim 16, wherein the heat treatment is carried out by heating said amorphous alloy at 450-700°C for 5 minutes to 24 hours.
18. The method of according to claim 16, wherein said heat treatment is carried out in a magnetic field.
19. An Fe-base soft magnetic alloy having the composition represented by the general formula:
(Fe1-aMa)100-x-y-z-.alpha.-.beta.-.gamma.CuxSiyBzM'.alpha.M".beta.X.gamma.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, M"
is at least one element selected from the group consisting of V, Cr, Mn, A?, elements in the platinum group, Sc, Y, rare earth elements, Au, Zn, Sn and Re, X is at least one element selected from the group consisting of C, Ge, P, Ga, Sb, In, Be and As, and a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30, 0.1?.alpha.?30, .beta.?10 and .gamma.?10, at least 50% of the alloy structure being fine crystalline particles having an average particle size of 1000.ANG.
or less.
(Fe1-aMa)100-x-y-z-.alpha.-.beta.-.gamma.CuxSiyBzM'.alpha.M".beta.X.gamma.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, M"
is at least one element selected from the group consisting of V, Cr, Mn, A?, elements in the platinum group, Sc, Y, rare earth elements, Au, Zn, Sn and Re, X is at least one element selected from the group consisting of C, Ge, P, Ga, Sb, In, Be and As, and a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30, 0.1?.alpha.?30, .beta.?10 and .gamma.?10, at least 50% of the alloy structure being fine crystalline particles having an average particle size of 1000.ANG.
or less.
20. The Fe-base soft magnetic alloy according to claim 19, wherein said a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.1, 0/1?x?3, 6?y?25, 2?z?25, 14?y+z?30, 0.1?.alpha.?10, .beta.?5 and .gamma.?5.
21. The Fe-base soft magnetic alloy according to claim 19, wherein said a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.1, 0.5?x?2, 10?y?25, 3?z?18, 18?y+z?28, 2?.alpha.?8, .beta.?5 and .gamma.?5.
22. The Fe-base soft magnetic alloy according to claim 19, wherein said a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.05, 0.5?x?2, 11?y?24, 3?z?9, 18?y+z?27, 2?.alpha.?8, .beta.?5 and .gamma.?5.
23. The Fe-base soft magnetic alloy according to claim 19, wherein the balance of said alloy structure is substantially amorphous.
24. The Fe-base soft magnetic alloy according to claim 19, wherein said alloy structure substantially consists of fine crystalline particles.
25. The Fe-base soft magnetic alloy according to claim 19, wherein said M' is Nb and/or Mo.
26. The Fe-base soft magnetic alloy according to claim 25, wherein said M' is Nb.
27. The Fe-base soft magnetic alloy according to claim 19, wherein said y and z satisfy 5?y+z?10 when 10?.alpha.?30.
28. The Fe-base soft magnetic alloy according to claim 19, wherein said y and z satisfy 0?z/y<1.
29. The Fe-base soft magnetic alloy according to claim 19, wherein X is C, and y+z+y satisfy 15?y+z+.gamma.?35 (.gamma.=0).
30. The Fe-base soft magnetic alloy according to claim 19, wherein said crystalline particles have an average particle size of 500.ANG. or less.
31. The Fe-base soft magnetic alloy according to claim 19, wherein said crystalline particles have an average particle size of 200.ANG. or less.
32. The Fe-base soft magnetic alloy according to claim 19, wherein said crystalline particles have an average particle size oE 50-200.ANG..
33. A method of producing an Fe-base soft magnetic alloy having the composition represented by the general formula:
(Fe1-aMa)100-x-y-z-.alpha.-.beta.-.gamma.CuxSiyBzM'.alpha.M".beta.X.gamma.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, M"
is at least one element selected from the group consisting of V, Cr, Mn, A?, elements in the platinum group, Sc, Y, rare earth elements, Au, Zn, Sn and Re, X is at least one element selected from the group consisting of C, Ge, P, Ga, Sb, In, Be and As, and a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30, 0.1?.alpha.?30 .beta.?10 and .gamma.?10, at least 50% of the alloy structure being fine crystalline particles having an average particle size of 1000.ANG.
or less, comprising the steps of:
(a) rapidly quenching a melt of the above composition to form an amorphous alloy; and (b) heat-treating said amorphous alloy to generate fine crystalline particles having an average particle size of 1000.ANG. or less.
(Fe1-aMa)100-x-y-z-.alpha.-.beta.-.gamma.CuxSiyBzM'.alpha.M".beta.X.gamma.
wherein M is Co and/or Ni, M' is at least one element selected from the group consisting of Nb, W, Ta, Zr, Hf, Ti and Mo, M"
is at least one element selected from the group consisting of V, Cr, Mn, A?, elements in the platinum group, Sc, Y, rare earth elements, Au, Zn, Sn and Re, X is at least one element selected from the group consisting of C, Ge, P, Ga, Sb, In, Be and As, and a, x, y, z, .alpha., .beta. and .gamma. respectively satisfy 0?a?0.5, 0.1?x?3, 0?y?30, 0?z?25, 5?y+z?30, 0.1?.alpha.?30 .beta.?10 and .gamma.?10, at least 50% of the alloy structure being fine crystalline particles having an average particle size of 1000.ANG.
or less, comprising the steps of:
(a) rapidly quenching a melt of the above composition to form an amorphous alloy; and (b) heat-treating said amorphous alloy to generate fine crystalline particles having an average particle size of 1000.ANG. or less.
34. The method according to claim 33, wherein said heat treatment is carried out by heating said amorphous alloy at 450-700°C for 5 minutes to 24 hours.
35. The method according to claim 33, wherein said heat treatment is carried out in a magnetic field.
Applications Claiming Priority (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP61-297938 | 1986-12-15 | ||
JP29793886 | 1986-12-15 | ||
JP5857787 | 1987-03-13 | ||
JP62-58577 | 1987-03-13 | ||
JP13799587 | 1987-06-01 | ||
JP62-137995 | 1987-06-01 |
Publications (1)
Publication Number | Publication Date |
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CA1323219C true CA1323219C (en) | 1993-10-19 |
Family
ID=27296627
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Application Number | Title | Priority Date | Filing Date |
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CA000553434A Expired - Lifetime CA1323219C (en) | 1986-12-15 | 1987-12-03 | Fe-base soft magnetic alloy and method of producing same |
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US (2) | US4881989A (en) |
EP (1) | EP0271657B1 (en) |
JP (1) | JPH0774419B2 (en) |
KR (1) | KR910003977B1 (en) |
CA (1) | CA1323219C (en) |
DE (1) | DE3779070D1 (en) |
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-
1987
- 1987-10-01 US US07/103,250 patent/US4881989A/en not_active Expired - Lifetime
- 1987-10-06 EP EP87114568A patent/EP0271657B1/en not_active Expired - Lifetime
- 1987-10-06 DE DE8787114568T patent/DE3779070D1/en not_active Expired - Lifetime
- 1987-12-03 CA CA000553434A patent/CA1323219C/en not_active Expired - Lifetime
- 1987-12-11 KR KR1019870014143A patent/KR910003977B1/en not_active IP Right Cessation
-
1990
- 1990-08-31 JP JP2231854A patent/JPH0774419B2/en not_active Expired - Lifetime
-
1991
- 1991-01-22 US US07/643,104 patent/US5160379A/en not_active Expired - Lifetime
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JPH03219009A (en) | 1991-09-26 |
EP0271657A3 (en) | 1989-06-07 |
KR880007787A (en) | 1988-08-29 |
US4881989A (en) | 1989-11-21 |
US5160379A (en) | 1992-11-03 |
JPH0774419B2 (en) | 1995-08-09 |
DE3779070D1 (en) | 1992-06-17 |
EP0271657B1 (en) | 1992-05-13 |
KR910003977B1 (en) | 1991-06-17 |
EP0271657A2 (en) | 1988-06-22 |
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