Magnetic core based on a nanocrystalline magnetic alloy
11264156 · 2022-03-01
Assignee
Inventors
Cpc classification
C22C38/002
CHEMISTRY; METALLURGY
H01F1/15333
ELECTRICITY
C21D1/04
CHEMISTRY; METALLURGY
C22C38/12
CHEMISTRY; METALLURGY
International classification
C21D8/12
CHEMISTRY; METALLURGY
C21D9/52
CHEMISTRY; METALLURGY
C21D1/04
CHEMISTRY; METALLURGY
C22C38/12
CHEMISTRY; METALLURGY
Abstract
A magnetic core includes a nanocrystalline alloy ribbon having a composition represented by FeCu.sub.xB.sub.ySi.sub.zA.sub.aX.sub.b, where 0.6≤x<1.2, 10≤y≤20, 0≤(y+z)≤24, and 0≤a≤10, 0≤b≤5, all numbers being in atomic percent, with the balance being Fe and incidental impurities, and where A is an optional inclusion of at least one element selected from Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W, and X is an optional inclusion of at least one element selected from Re, Y, Zn, As, In, Sn, and rare earth elements. The nanocrylstalline alloy ribbon has a local structure such that nanocrystals with average particle sizes of less than 40 nm are dispersed in an amorphous matrix and are occupying more than 30 volume percent of the ribbon.
Claims
1. A magnetic core comprising: a nanocrystalline alloy ribbon having a composition represented by Fe.sub.bal,Cu.sub.xB.sub.ySi.sub.zA.sub.aX.sub.b, where 0.6 at. %≤x<1.2 at. %, 10 at. %≤y≤20 at. %, 0 at. %<z≤10 at. %, 10 at. %<(y+z)≤24 at. %, 0 at. %≤a≤10 at. %, and 0 at. %≤b≤5 at. %, at. % being atomic percent, and where A is an optional inclusion of at least one element selected from Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W, X is an optional inclusion of at least one element selected from Re, Y, Zn, As, In, Sn, and rare earth elements, and a total content of Ti, Mo, Nb, Zr, Ta and Hf in the composition is below 0.3 atomic percent, the nanocrystalline alloy ribbon having a heat-treated local structure including nanocrystals with average particle sizes of less than 40 nm dispersed in an amorphous matrix and are occupying more than 30 volume percent of the nanocrystalline alloy ribbon, and the magnetic core having a coercivity of less than 4 A/m; and a magnetic induction at 80 A/m exceeding 1.6 T and below 1.75 T.
2. The magnetic core of claim 1, wherein the nanocrystalline alloy ribbon has been subjected to heat treatment at a temperature in a range of from 430° C. to 550° C. at a heating rate of 10° C./s or more for less than 30 seconds, with a tension between 1 MPa and 500 MPa applied during the heat treatment; and the nanocrystalline alloy ribbon has been wound, after the heat treatment, to form a wound core.
3. The magnetic core of claim 2, wherein the wound core has been further heat-treated in a wound form at a temperature from 400° C. to 500° C. for 1.8 ks-10.8 ks in a magnetic field of less than 4 kA/m applied along the wound core's circumference direction.
4. The magnetic core of claim 1, wherein the magnetic core is a wound core, and a round portion of the magnetic core is comprised of a ribbon whose radius of curvature is between 10 mm and 200 mm when let loose, and the round portion of the magnetic core is such that a ribbon relaxation rate defined by (2-R.sub.w/R.sub.f) is larger than 0.93, where R.sub.w and R.sub.f are, respectively, ribbon radius of curvature prior to ribbon release and ribbon radius of curvature after ribbon release and when the magnetic core is free of constraint.
5. The magnetic core of claim 2, wherein the nanocrystalline alloy ribbon has been heat-treated by an average heating rate of more than 10° C./s from room temperature to a predetermined holding temperature which exceeds 430° C. and less than 550° C., and then held at the holding temperature for a holding time of less than 30 seconds.
6. The magnetic core of claim 2, wherein the nanocrystalline alloy ribbon has been heat-treated by an average heating rate of more than 10° C./s from 300° C. to a predetermined holding temperature which exceeds 450° C. and is less than 520° C., and then held at the holding temperature for a holding time of less than 30 seconds.
7. The magnetic core of claim 6, wherein the holding time is less than 20 seconds.
8. The magnetic core of claim 1, wherein the composition of the nanocrystalline alloy ribbon contains at least 78 at. % Fe.
9. The magnetic core of claim 1, wherein the composition of the nanocrystalline alloy ribbon contains from 0.01 atomic percent to 10 atomic percent of at least one selected from Ni, Mn, Co, V, Cr, Ti, Mo, and W.
10. The magnetic core of claim 9, wherein the composition of the nanocrystalline alloy contains one or more selected from Nb, Zr, Ta and Hf in an amount that is at least 0.01 atomic percent and below 0.3 atomic percent in total.
11. The magnetic core of claim 1, wherein in the composition of the nanocrystalline alloy ribbon, a total amount of Re, Y, Zn, As, In, Sn, and rare earth elements is in a range of from 0 atomic percent to less than 2.0 atomic percent.
12. The magnetic core of claim 11, wherein the total amount of Re, Y, Zn, As, In, Sn, and rare earth elements is in a range of from 0 atomic percent to less than 1.0 atomic percent.
13. An electrical power distribution transformer comprising the magnetic core of claim 1.
14. A magnetic inductor for electrical power management operated at commercial and high frequencies, comprising the magnetic core of claim 1.
15. A transformer utilized in power electronics, comprising the magnetic core of claim 1.
16. A device comprising the magnetic core of claim 1, the magnetic core having a core loss of 0.2 W/kg-0.5 W/kg at 60 Hz and 1.6 T and a core loss of 0.15 W/kg-0.4 W/kg at 50 Hz and 1.6 T, and having a B.sub.800 exceeding 1.7 T, and the device being an electrical power distribution transformer, or a magnetic inductor for electrical power management operated at commercial and high frequencies.
17. A device comprising the magnetic core of claim 1, the magnetic core having a core loss of less than 30 W/kg at 10 kHz and an operating induction level of 0.5 T, and having a B.sub.800 exceeding 1.7 T, and the device being a magnetic inductor for electrical power management operated at commercial and high frequencies, or a transformer utilized in power electronics.
18. The magnetic core of claim 1, having B.sub.f/B.sub.800 exceeding 0.8, and B.sub.800 exceeding 1.7 T.
19. A method of manufacturing the magnetic core of claim 1, comprising: producing the nanocrystalline alloy ribbon by heat treating a rapidly solidified ribbon, having the alloy composition, at a temperature in a range of from 430° C. to 550° C. at a heating rate of 10° C./s or more for less than 30 seconds, with a tension between 1 MPa and 500 MPa applied during the heat treating; and after the heat treating, winding the nanocrystalline alloy ribbon to form a wound core.
20. The method of claim 19, further comprising: after the winding the nanocrystalline alloy ribbon, further heat treating the wound core in wound form at a temperature from 400° C. to 500° C. for 1.8 ks 10.8 ks in a magnetic field of less than 4 kA/m applied along the wound core's circumference direction.
21. The method of claim 19, wherein the heat treating before the winding is performed by heating the rapidly solidified ribbon at an average heating rate of more than 10° C./s from room temperature to a predetermined holding temperature which exceeds 430° C. and less than 550° C., and holding the heated ribbon at the holding temperature for a holding time of less than 30 seconds.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The invention will be more fully understood and further advantages will become apparent when reference is made to the following detailed description of the embodiments and the accompanying drawings in which:
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DESCRIPTION OF EMBODIMENTS
(14) A ductile metallic ribbon as used in embodiments of the invention may be cast by a rapid solidification method described in U.S. Pat. No. 4,142,571. The ribbon form is suitable for post ribbon-fabrication heat treatment, which is used to control the magnetic properties of the cast ribbon.
(15) This composition of the ribbon used in embodiments of the invention comprises Cu in an amount of 0.6 to 1.2 atomic percent, B in an amount of 10 to 20 atomic percent, and Si in an amount greater than 0 atomic percent and up to 10 atomic percent, where the combined content of B and Si ranges from 10 through 24 atomic percent. The alloy may also comprise, in an amount of up to 0.01-10 atomic percent (including values within this range, such as a values in the range of 0.01-3 and 0.01-1.5 at %), at least one element selected from the group of Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W. When Ni is included in the composition, Ni may be in the range of 0.1-2 or 0.5-1 atomic percent. When Co is included, Co may be included in the range of 0.1-2 or 0.5-1 atomic percent. When an element selected from the group of Ti, Zr, Nb, Mo, Hf, Ta and W is included, the total content of these elements may be at any value below 0.4 (including any value below 0.3, and below 0.2) atomic percent in total. The alloy may also comprise, in an amount of any value up to and less than 5 atomic percent (including values less up to and less than 2, 1.5, and 1 atomic percent), at least one element selected from the group of Re, Y, Zn, As, In, Sn, and rare earths elements.
(16) Each of the aforementioned ranges for the at least one element selected from the group of Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W (including the individually given ranges for Co and Ni) may coexist with each of the above-given ranges for the at least one element selected from the group of Re, Y, Zn, As, In, Sn, and rare earths elements. In any of the compositional configurations given above, the element P may be excluded from the alloy composition. All of the compositional configurations may be implemented subject to the proviso that the Fe content is in an amount of at least 75, 77 or 78 atomic percentage.
(17) An example of one composition range suitable for embodiments of the present invention is 80-82 at. % Fe, 0.8-1.1 at. % or 0.9-1.1 at. % Cu, 3-5 at. % Si, 12-15 at. % B, and 0-0.5 at. % collectively constituted of one or more elements selected from the group of Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W, where the aforementioned atomic percentages are selected so as to sum to 100 at %, aside from incidental or unavoidable impurities.
(18) The alloy composition may consist of or consist essentially of only the elements specifically named in the preceding two paragraphs, in the given ranges, along with incidental impurities. The alloy composition may also consist of or consist essentially of only the elements Fe, Cu, B, and Si, in the above given ranges for these particular elements, along with incidental impurities. The presence of any incidental impurities, including practically unavoidable impurities, is not excluded by any composition of the claims. If any of the optional constituents (Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta, W, Re, Y, Zn, As, In, Sn, and rare earths elements) are present, they may be present in an amount that is at least 0.01 at. %
(19) In embodiments of the invention, the chemical composition of the ribbon can be expressed as Fe.sub.100-x-y-zCu.sub.xB.sub.ySi.sub.z where 0.6≤x<1.2, 10≤y≤20, and 10≤(y+z)≤24, the numbers being in atomic percent. These alloys according to embodiments of the present invention are designated as Q-type alloys in the present application.
(20) A Cu content of 0.6≤x<1.2 is utilized because Cu atoms formed clusters serving as seeds for fine crystalline particles of bcc Fe, if x≥1.2. The size of such clusters, which affected the magnetic properties of a heat-treated ribbon, was difficult to control. Thus, x is set to be below 1.2 atomic percent. Since a certain amount of Cu was required to induce nanocrystallization in the ribbon by heat-treatment, it was determined that Cu≥0.6.
(21) Because of the positive heat of mixing in the amorphous Fe—B—Si matrix, Cu atoms tended to cluster to reduce boundary energy between the matrix and the Cu cluster phases. In related art alloys, elements such as P or Nb were added to control the diffusion of Cu atoms in the alloys. These elements may be eliminated or minimized in the alloys in embodiments of the present invention as they reduced the saturation magnetic inductions in the heat-treated ribbon. Related art alloys having these elements are classified as P-type alloys in the present disclosure. Therefore, either one or both of the elements P and Nb may be absent from the alloy, or absent except in amounts that are incidental or unavoidable. Alternatively, instead of having P be absent, P may be included in the minimized amounts discussed in this disclosure.
(22) Instead of controlling Cu diffusion by adding P or Nb to the alloys as described above, the heat-treatment process is modified in such a way that rapid heating of the ribbon did not allow for Cu atoms to have enough time to diffuse.
(23) In the previously recited composition of Fe.sub.100-x-y-zCu.sub.xB.sub.ySi.sub.z(0.6≤x<1.2, 10≤y≤20, 0<z≤10, 10≤(y+z)≤24), the Fe content should exceed or be at least 75 atomic percent, preferably 77 atomic percent and more preferably 78 atomic percent in order to achieve a saturation induction of more than 1.7 T in a heat-treated alloy containing bcc-Fe nanocrystals, if such saturation induction is desired. As long as the Fe content is enough to achieve the saturation induction exceeding 1.7 T, incidental impurities commonly found in Fe raw materials were permissible. These amounts of Fe being greater than 75, 77, or 78 atomic percent may be implemented in any composition of this disclosure, independently of the inclusion of Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W, and of Re, Y, Zn, As, In, Sn, and rare earths elements discussed below.
(24) In the previously recited composition of Fe.sub.100-x-y-zCu.sub.xB.sub.ySi.sub.z(0.6≤x<1.2, 10≤y≤20, 0<z≤10, 10≤(y+z)≤24), up to from 0.01 atomic percent to 10 atomic percent, preferably up to 0.01-3 atomic percent and most preferably up to 0.01-1.5 atomic percent of the Fe content denoted by Fe.sub.100-x-y-z may be substituted by at least one selected from the group of Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W. Elements such as Ni, Mn, Co, V and Cr tended to be alloyed into the amorphous phase of a heat-treated ribbon, resulting in Fe-rich nanocrystals with fine particle sizes and, in turn, increasing the saturation induction and enhancing the soft magnetic properties of the heat-treated ribbon. The presence of these elements (including in the ranges of individual elements discussed below) may exist in combination with the total Fe content being in an amount greater than 75, 77 or 78 atomic percentage.
(25) Of the Fe substitution elements Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W discussed above, Co and Ni additions allowed increase of Cu content, resulting in finer nanocrystals in the heat-treated ribbon and, in turn, improving the soft magnetic properties of the ribbon. In the case of Ni, its content was preferably from 0.1 atomic percent to 2 atomic percent and more preferably from 0.5 to 1 atomic percent. When Ni content was below 0.1 atomic percent, ribbon fabricability was poor. When Ni content exceeded 2 atomic percent, saturation induction and coercivity in the ribbon were reduced. In the case of Co addition, the Co content was preferably between 0.1 atomic percent and 2 atomic percent and more preferably between 0.5 atomic percent and 1 atomic percent.
(26) Furthermore, of the Fe substitution elements of Ni, Mn, Co, V, Cr, Ti, Zr, Nb, Mo, Hf, Ta and W discussed above, elements such as Ti, Zr, Nb, Mo, Hf, Ta and W tended to be alloyed into the amorphous phase of a heat-treated ribbon, contributing to the stability of the amorphous phase and improving the soft magnetic properties of the heat-treated ribbon. However, the atomic sizes of these elements were larger than other transition metals such as Fe and soft magnetic properties in the heat-treated ribbon were degraded when their contents were large. Therefore, it was preferred that the content of these elements was below 0.4 atomic percent. Their contents were preferably below 0.3 atomic percent or more preferably below 0.2 atomic percent in total.
(27) In the previously recited composition of Fe.sub.100-x-y-zCu.sub.xB.sub.ySi.sub.z(0.6≤x<1.2, 10≤y≤20, 0<z≤10, 10≤(y+z)≤24), less than 5 atomic percent or more preferably less than 2 atomic percent of Fe denoted by Fe.sub.100-x-y-z may could be replaced by one from the group of Re, Y, Zn, As, In, Sn, and rare earths elements. When a high saturation induction was desired, the contents of these elements were preferably less than 1.5 atomic percent or more preferably less than 1.0 atomic percent.
(28) The ribbon, in the compositions mentioned above, can be subjected to a first heat treatment, described as follows. The ribbon is heated with a heating rate exceeding 10° C./s to a predetermined holding temperature. When the holding temperature is near 300° C., the heating rate generally must exceed 10° C./s, as it considerably affects the magnetic properties in the heat-treated ribbon. It is preferred that the holding temperature exceed (T.sub.x2−50) ° C., where T.sub.x2 is the temperature at which crystalline particles precipitated. It is preferred that the holding temperature be higher than 430° C. The temperature T.sub.x2 can be determined from a commercially available differential scanning calorimeter (DSC). The alloys of embodiments of the present invention crystallize in two steps when heated with two characteristic temperatures. At the higher characteristic temperature, a secondary crystalline phase starts to precipitate, this temperature being termed T.sub.x2 in the present disclosure. When the holding temperature was lower than 430° C., precipitation and subsequent growth of fine crystalline particles was not sufficient. The highest holding temperature, however, was lower than 530° C. which corresponded to T.sub.x2 of the alloys of embodiments of the present invention. The holding time was preferred to be less than 30 seconds or more preferred to be less than 20 seconds or most preferred to be less than 10 seconds. Some examples of the above process are given in Examples 1 and 2.
(29) The heat-treated ribbon of the above paragraph was wound into a magnetic core which in turn was heat treated between 400° C. and 500° C. for the duration between 900 sec and 10.8 ks. For sufficient stress relief, the heat-treatment period was preferably more than 900 sec or more preferably more than 1.8 ks. When a higher productivity was desired, the heat-treatment period was less than 10.8 ks or preferably less than 5.4 ks. This additional process was found to homogenize the magnetic properties of a heat-treated ribbon. Example 3 shows some of the results (
(30) In the heat-treatment process, a magnetic field was applied to induce magnetic anisotropy in the ribbon. The field applied was high enough to magnetically saturate the ribbon and was preferably higher than 0.8 kA/m. The applied field was either in DC, AC or pulse form. The direction of the applied field during heat-treatment was predetermined depending on the need for a square, round or linear BH loop. When the applied field was zero, a BH behavior with medium squareness ratio of 50%-70% resulted. Magnetic anisotropy was an important factor in controlling the magnetic performance such as magnetic losses in a magnetic material and ease of controlling magnetic anisotropy by heat-treatment of an alloy of embodiments of the present invention was advantageous.
(31) Instead of a magnetic field applied during the heat-treatment, mechanical tension was alternatively applied. This resulted in tension-induced magnetic anisotropy in the heat-treated ribbon. An effective tension was higher than 1 MPa and less than 500 MPa. Examples of BH loops taken on the ribbon heat-treated under tension are shown in
EXAMPLE 1
(32) A rapidly-solidified ribbon having a composition of Fe.sub.81Cu.sub.1.0Si.sub.4B.sub.14 was traversed on a 30 cm-long bronze plate heated at 490° C. for 3-15 seconds with a ribbon tension at 25 MPa. It took 5-6 seconds for the ribbon to reach the bronze-plate temperature of 490° C., resulting in a heating rate of 50-100° C./sec. The heat-treated ribbon was characterized by a commercial BH loop tracer and the result is given in
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EXAMPLE 2
(35) During first heat-treatment of a ribbon according to embodiments of the present invention, a radius of curvature developed in the ribbon, although the heat treated ribbon is relatively flat. To determine the range of radius of ribbon curvature, R (mm), in a heat-treated ribbon in which B.sub.80/B.sub.800 was greater than 0.90, B.sub.80/B.sub.800 ratio was examined as a function of ribbon radius of curvature which was changed by winding the heat treated ribbon on rounded surface with known radius of curvature. The results are listed in Table 1. The data in Table 1 are summarized by B.sub.80/B.sub.800=0.0028R+0.48. The data in Table 1 is used to design a magnetic core, for example, made from laminated ribbon.
(36) TABLE-US-00001 TABLE 1 Radius of ribbon curvature versus B.sub.80/B.sub.800 Sample R, Radius of Ribbon Curvature (mm) B.sub.80/B.sub.800 1 ∞ 0.98 2 200 0.92 3 150 0.89 4 100 0.72 5 58 0.65 6 25 0.55 7 12.5 0.52
(37) Sample 1 corresponds to the flat ribbon case of
EXAMPLE 3
(38) Strip samples of Fe.sub.81Cu.sub.1Mo.sub.0.2Si.sub.4B.sub.13.8 alloy ribbon were annealed on a hot plate first with a heating rate of more than 50° C./s in a heating bath at 470° C. for 15 sec., followed by secondary annealing at 430° C. for 5,400 seconds in a magnetic field of 1.5 kA/m. Another sample of trips of the same chemical composition were annealed first with a heating rate of more than 50° C./s in a heating bath at 481° C. for 8 seconds and with a tension of 3 MPa, followed by secondary annealing at 430° C. for 5,400 seconds with a magnetic field of 1.5 kA/m. Examples of BH loops taken on these strips before and after the secondary annealing are shown in
EXAMPLE 4
(39) A ribbon having the aforementioned Fe.sub.100-x-y-zCu.sub.xB.sub.ySi.sub.z composition was first heat-treated at temperatures between 470° C. and 530° C. by directly contacting the ribbon on a surface, of brass or Ni-plated copper, having a radius of curvature of 37.5 mm, followed by rapid heating of the ribbon at a heating rate of greater than 10° C./s above 300° C., with contacting time between 0.5 s and 20 s. The resulting ribbon had a radius of curvature between 40 mm and 500 mm. The heat-treated ribbon was then wound into a toroidal core, which was heat-treated at 400° C.-500° C. for 1.8 ks-5.4 ks (kilosecond).
(40) A toroidal core according to the preceding paragraph was wound such that the ribbon radius of curvature was in a range of from 10 mm to 200 mm when let loose and that the ribbon relaxation rate defined by (2−R.sub.w/R.sub.f) was larger than 0.93. Here, R.sub.W and R.sub.f are, respectively, ribbon radius of curvature prior to ribbon release and ribbon radius of curvature after its release and free of constraint.
(41) Toroidal cores having outside diameters (OD)=42.0 mm-130.5 mm, inside diameters (ID)=40.0 mm-133.0 mm and heights (H)=25.4 mm-50.8 mm were made from the annealed ribbon having BH loops generally characterized by
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(43) TABLE-US-00002 TABLE 2 Physical and magnetic properties of toroidal cores of embodiments of the present invention. H = 25.4 mm for Alloys A, B and C; t.sub.c = ribbon contacting time; P.sub.16/60 and P.sub.16/50 are core loss at 1.6 T, and 60 Hz and 50 Hz excitation, respectively; B.sub.r is remanent and B.sub.800 is induction at 800 A/m. Core Secondary Core Core Size Primary Anneal Anneal Loss Loss OD-ID T (° C.)-t.sub.c (sec)- T (° C.)-t.sub.c (ks)- P.sub.16/60 P.sub.16/50 B.sub.800 Hc Alloy (mm) Tension (MPa) Field (kA/m) (W/kg) (W/kg) (T) B.sub.r/B.sub.800 (A/m) A 96.0-89.4 492-1-3 430-3.6-3.5 0.30 1.70 0.81 3.7 A 96.0-90.0 504-1-3 430-3.6-3.5 0.26 0.22 1.71 0.86 2.2 A 114.0-71.0 500-2.2-3 430-3.6-3.5 0.31 0.24 1.70 0.77 2.6 A 72.0-70.0 483-4-15 430-3.6-4.5 0.16 1.75 0.90 2.2 A 72.0-70.0 495-6-8 430-3.6-4.5 0.18 1.70 0.80 2.8 A 96.1-90.3 524-1.1-3 430-3.6-3.5 0.24 1.71 0.72 2.6 A 117.0-115.0 483-6-8 No second 0.22 1.74 0.75 3.3 anneal A 130.5-133.0 483-6-8 No second 0.24 1.70 0.80 3.3 anneal B 91.6-88.9 474-6-8 430-3.6-3.5 0.29 1.75 0.90 2.5 B 93.3-89.6 485-2.2-3 430-3.6-3.5 0.34 0.28 1.74 0.96 2.1 B 90.7-88.9 483-6-8 430-3.6-3.5 0.31 1.78 0.87 2.3 B 91.5-88.9 489-6-8 430-3.6-3.5 0.28 1.77 0.85 2.2 C 117-153 499-1-5 430-3.6-3.5 0.37 0.29 1.73 0.90 2.2 D 98.5-90.0 500-1-3 430-3.6-3.5 0.38 0.30 1.70 0.92 2.2
(44) Table 2 indicates that the alloys of embodiments of the present invention, when heat-treated, have saturation induction ranging from 1.70 T to 1.78 T and coercivity H.sub.c ranging from 2.2 A/m to 3.7 A/m. These are to be compared with B.sub.s=2.0 T and H.sub.c=8 A/m for 3% silicon steel, indicating that a magnetic core based on an alloy of embodiments of the present invention shows a core loss at 50/60 Hz operation of about ½ that of a conventional silicon steel. The data in Table 2 give core loss at 50 Hz/1.6 T and 60 Hz/1.6 T of 0.16 W/kg-0.31 W/kg and 0.26 W/kg-0.38 W/kg, respectively. Core loss at 50 Hz and 60 Hz at different induction levels are shown in
EXAMPLE 5
(45) High frequency magnetic properties of the toroidal cores of Example 4 were evaluated according to the ASTM A927 Standard. An example of core loss P(W/kg) versus operating flux B.sub.m(T) is shown in
EXAMPLE 6
(46) A rapidly quenched ribbon was heat treated according to the first heat treatment process described earlier. The heat-treated ribbon was then wound into an oblong-shaped core as shown in
EXAMPLE 7
(47) A 25.4 mm-wide ribbon with a chemical composition of Fe.sub.81.8Cu.sub.0.8Mo.sub.0.2Si.sub.4.2B.sub.13 was rapidly heated up to 500° C. within 1 second under a tension of 5 MPa and was air-cooled, as shown by the heating profile of
EXAMPLE 8
(48) 180° bend ductility tests were taken on the alloys of embodiments of the present invention and two alloys of the '531 publication (as comparative examples), as shown in Table 3 below. The 180° bend ductility test is commonly used to test if ribbon-shaped material breaks or cracks when bent by 180°. As shown, the products of the embodiments of the present invention did not exhibit failure in the bending test.
(49) TABLE-US-00003 TABLE 3 Composition 180° bending Fe.sub.bal.Cu.sub.0.6Si.sub.4B.sub.14 passed Fe.sub.bal.Cu.sub.1.0Si.sub.4B.sub.14 passed Fe.sub.bal.Cu.sub.1.1Si.sub.4B.sub.14 passed Fe.sub.bal.Cu.sub.1.15Si.sub.4B.sub.14 partially possible Fe.sub.bal.Cu.sub.0.8Mo.sub.0.2Si.sub.4.2B.sub.13 passed Fe.sub.bal.Cu.sub.1.0Mo.sub.0.2Si.sub.4.2B.sub.13 passed Fe.sub.bal.Cu.sub.1.0Mo.sub.0.2Si.sub.4B.sub.14 passed Fe.sub.bal.Cu.sub.1.0Mo.sub.0.5Si.sub.4B.sub.14 passed Fe.sub.bal.Cu.sub.1.2Si.sub.4B.sub.14 failed (′531 publication product) Fe.sub.bal.Cu.sub.1.3Si.sub.4B.sub.14 failed (′531 publication product)
(50) As used throughout this disclosure, the term “to” includes the endpoints of the range. Therefore, “x to y” refers to a range including x and including y, as well as all of the intermediate points in between; such intermediate points are also part of this disclosure. Moreover, one skilled in the art would also understand that deviations in numerical quantities are possible. Therefore, whenever a numerical value is mentioned in the specification or claims, it is understood that additional values that are about such numerical value or approximately such numerical value are also within the scope of the invention.
(51) Although a few embodiments have been shown and described, it would be appreciated by those skilled in the art that changes may be made in these embodiments without departing from the principles and spirit of the invention, the scope of which is defined in the claims and their equivalents.