US3652416A - Oxide magnetic materials - Google Patents
Oxide magnetic materials Download PDFInfo
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- US3652416A US3652416A US872094A US3652416DA US3652416A US 3652416 A US3652416 A US 3652416A US 872094 A US872094 A US 872094A US 3652416D A US3652416D A US 3652416DA US 3652416 A US3652416 A US 3652416A
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- oxide
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- 239000000696 magnetic material Substances 0.000 title description 11
- XOLBLPGZBRYERU-UHFFFAOYSA-N tin dioxide Chemical compound O=[Sn]=O XOLBLPGZBRYERU-UHFFFAOYSA-N 0.000 claims abstract description 20
- FUJCRWPEOMXPAD-UHFFFAOYSA-N lithium oxide Chemical compound [Li+].[Li+].[O-2] FUJCRWPEOMXPAD-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229910001947 lithium oxide Inorganic materials 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims description 29
- 229910001289 Manganese-zinc ferrite Inorganic materials 0.000 claims description 15
- JIYIUPFAJUGHNL-UHFFFAOYSA-N [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Mn++].[Mn++].[Mn++].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Zn++].[Zn++] Chemical compound [O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[O--].[Mn++].[Mn++].[Mn++].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Fe+3].[Zn++].[Zn++] JIYIUPFAJUGHNL-UHFFFAOYSA-N 0.000 claims description 15
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 4
- 229910052681 coesite Inorganic materials 0.000 claims 1
- 229910052906 cristobalite Inorganic materials 0.000 claims 1
- XUCJHNOBJLKZNU-UHFFFAOYSA-M dilithium;hydroxide Chemical compound [Li+].[Li+].[OH-] XUCJHNOBJLKZNU-UHFFFAOYSA-M 0.000 claims 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims 1
- 239000000377 silicon dioxide Substances 0.000 claims 1
- 235000012239 silicon dioxide Nutrition 0.000 claims 1
- 229910052682 stishovite Inorganic materials 0.000 claims 1
- 229910052905 tridymite Inorganic materials 0.000 claims 1
- XLOMVQKBTHCTTD-UHFFFAOYSA-N Zinc monoxide Chemical compound [Zn]=O XLOMVQKBTHCTTD-UHFFFAOYSA-N 0.000 abstract description 30
- 229910000859 α-Fe Inorganic materials 0.000 abstract description 23
- 239000011787 zinc oxide Substances 0.000 abstract description 15
- WJZHMLNIAZSFDO-UHFFFAOYSA-N manganese zinc Chemical compound [Mn].[Zn] WJZHMLNIAZSFDO-UHFFFAOYSA-N 0.000 abstract description 8
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 abstract description 6
- AMWRITDGCCNYAT-UHFFFAOYSA-L hydroxy(oxo)manganese;manganese Chemical compound [Mn].O[Mn]=O.O[Mn]=O AMWRITDGCCNYAT-UHFFFAOYSA-L 0.000 abstract description 4
- 239000002253 acid Substances 0.000 abstract description 2
- 230000000694 effects Effects 0.000 description 16
- 239000000654 additive Substances 0.000 description 9
- 239000000292 calcium oxide Substances 0.000 description 9
- ODINCKMPIJJUCX-UHFFFAOYSA-N calcium oxide Inorganic materials [Ca]=O ODINCKMPIJJUCX-UHFFFAOYSA-N 0.000 description 9
- 230000000996 additive effect Effects 0.000 description 7
- 239000003795 chemical substances by application Substances 0.000 description 5
- 238000005245 sintering Methods 0.000 description 5
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical compound [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- BRPQOXSCLDDYGP-UHFFFAOYSA-N calcium oxide Chemical compound [O-2].[Ca+2] BRPQOXSCLDDYGP-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N iron Substances [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 239000012299 nitrogen atmosphere Substances 0.000 description 3
- 229910052760 oxygen Inorganic materials 0.000 description 3
- 239000001301 oxygen Substances 0.000 description 3
- 238000001816 cooling Methods 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 238000007689 inspection Methods 0.000 description 2
- 229910052744 lithium Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 238000012986 modification Methods 0.000 description 2
- 230000004048 modification Effects 0.000 description 2
- 230000035699 permeability Effects 0.000 description 2
- 229910052814 silicon oxide Inorganic materials 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 238000006842 Henry reaction Methods 0.000 description 1
- WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- 229910052785 arsenic Inorganic materials 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 239000002612 dispersion medium Substances 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 235000006748 manganese carbonate Nutrition 0.000 description 1
- 239000011656 manganese carbonate Substances 0.000 description 1
- 229940093474 manganese carbonate Drugs 0.000 description 1
- 229910000016 manganese(II) carbonate Inorganic materials 0.000 description 1
- XMWCXZJXESXBBY-UHFFFAOYSA-L manganese(ii) carbonate Chemical compound [Mn+2].[O-]C([O-])=O XMWCXZJXESXBBY-UHFFFAOYSA-L 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B35/00—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products
- C04B35/01—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics
- C04B35/26—Shaped ceramic products characterised by their composition; Ceramics compositions; Processing powders of inorganic compounds preparatory to the manufacturing of ceramic products based on oxide ceramics based on ferrites
- C04B35/2658—Other ferrites containing manganese or zinc, e.g. Mn-Zn ferrites
Definitions
- OXIDE MAGNETIC MATERIALS lnventors lzuru Sugano; Tsuneo Akashi; Tetsujin Matsubara; Yoshihiro Kenmoku; Taneaki Okuda, all of Tokyo, Japan Assignee: Nippon Electric Company, Limited,
- ABSTRACT Manganese-zinc ferrites consisting essentially of manganese oxide, zinc oxide and iron oxide and small but effective amount of stannic oxide and lithium oxide ranging up to about 3.2 percent by weight of stannic acid and up to about 0.125 percent by weight of lithium oxide.
- Manganese-zinc ferrites have found extensive applications as excellent soft magnetic materials for communications use in the frequency band near 100 KHZ. and various improvements in magnetic properties have been attempted to cope with their diversified application fields. In keeping with the present-day rapid progress of communications equipment, miniaturization and high performance of magnetic cores have been in great demand, with the result that improvements in material and performance of ferrites themselves have become an important problem. 7
- manganese-zinc ferrites with quality factors (tan 8/p.) and hysteresis loss factors (h10) less than 2 X 10 and at 100 kl-lz., respectively, have hitherto not been attainable.
- the quality factor and the hysteresis loss factor are defined according to the following equation:
- FIGS. 1 to 18 illustrate the manner in which the magnetic properties of the ferrites are improved by this invention.
- the present invention resides in the addition of stannic oxide (SnO and lithium oxide (Li O), in combination to the manganese-zinc ferrite composition in amounts that effectively improves the loss characreristics of the ferrites, i.e., both the quality factor and the hysteresis loss factor.
- Example 1 Before describing in detail the subject matter of this invention, it will be noted hereinafter from Example 1 that a remarkable effect can be obtained for improvements in both the quality and the hysteresis loss factors when a compound of tin and a compound of lithium are added together to a manganese-zinc ferrite having a basic composition containing 55.9 mol percent Fe O 38.0 mol percent MnO, and 6.1 mol percent ZnO as the main constituents so that the additives may ultimately take the form of SD02 and U 0.
- Example 7 it will be noted that the effect of the presence of SnO, and U 0 in the ferrite composition is markedly noticeable even when a special heat treatment is applied for improving magnetic properties as disclosed in Japanese patent application, No. 62961/1967.
- Example 8 it will also be noted that the effect of the addition of Sn0 and LL 0 per se remains substantially unchanged even when another combination of additives, such as CaO and $0, is present in varying amounts in the manganese-zinc ferrite composition.
- iron oxide, manganese carbonate, zinc oxide, calcium oxide, and silicon oxide, together with the essential additive agents of this invention, i.e., stannic oxide and lithium carbonate, are individually weighed so as to obtain a predetermined composition and these compounds were mixed and pulverized for about 60 hours in a ball-mill using alcohol as a dispersion medium, followed by presintering the mixture for about 4 hours at about 800C, pressing into a desired shape, firing for about 8 hours at about 1180C in a nitrogen atmosphere containing 0.4 percent oxygen and then cooling. During cooling, the oxygen content in the nitrogen atmosphere is controlled.
- FIGS. 1 and 2 in combination demonstrate that the effect of U 0 and Sn0 added together to a manganese-zinc ferrite having a basic composition of 38.0 mol percent MnO, 6.10 mol percent ZnO, and 55.90 mol percent Fe,,0 is excellent insofar as improvements in the loss characteristics tan tS/p. and h are concerned.
- An inspection of these graphs readily reveals the following: Both tan 8/ and h are markedly improved by the addition of SnO and Li O in small but effective amounts ranging from:
- FIGS. 3 and 4 illustrate in combination the effect of Li,0 and SnO, added together to a manganese-zinc ferrite having a basic composition of 36.0 mol percent MnO, 8.8 mol percent ZnO, and 55.2 mol percent re o,
- very good oxide magnetic materials meeting the two conditions tan ti/u 1.0 X 10", and h 3 can be obtained by the addition of small but effective amounts of from 0.6 to 2.7 wt. percent SnO and from 0.01 to 0.1 wt. percent Li O.
- Such markedly improved magnetic properties have heretofore not been realized.
- FIGS. 5 and 6 illustrate in combination the effect of Li,0 and SnO added together to a manganese-zinc ferrite having a basic composition of 36.0 mol percent MnO, 9.5 mol percent ZnO, and 54.5 mol percent R 0
- excellent oxide magnetic materials meeting the two conditions tan 6/ 1.0 X 10', and h 3 at 100 KHz. are obtained by the addition of small but effective amounts of SnO, and U 0 in the ranges expressed as 2.0 wt.% E SnO- 3.2 wt.% 0.0 1wt.% Li O 5 0.06 wt.
- FIGS. 7 and 8 indicate in combination the effect of U 0 and Sn0 added together to a manganese-zinc ferrite having a basic composition of 34.0 mol percent MnO, 1 1.60 mol percent ZnO, and 54.4 mol percent Fe O
- the loss characteristics of the ferrites can be markedly improved by the addition of small but effective amounts of SnO and U 0 expressed as 0.8 wt.% Sn0 2.3 wt.% 0 wt.% Li 0.07 wt.% and excellent oxide magnetic materials meeting the two conditions, tan 8],; l.2'X 10' and h 4, at 100 KHz. can be ob tained.
- FIGS. 9 and 10 indicate in combination the effect of SnO and Li o added together to a manganese-zinc ferrite having a basic composition of 34.0 mol percent MnO, 10.75 mol percent ZnO, and 55.25 mol percent Fe O
- excellent oxide magnetic materials meeting the two conditions tan 8/11. 1.2 X 10 and h 4 heretofore have not been realized by known methods, can be obtained by the addition of small but effective amounts of SnO and U expressed as 0 wt. SnO a 1.4 wt.% 0 wt. Li O 0.06 wt.%
- FIGS. 11 and 12 indicate in combination the effect of SnO and Li O added together to a manganese-zinc ferrite having a basic composition of 32.0 mol percent MnO, 13.15 mol percent ZnO, and 54.85 mol percent Fe O
- excellent oxide magnetic materials meeting the two conditions, tan Blp. 1.3
- X l0 and h at 100 KHz. can be obtained by the addition of small but effective amounts of SnO and U 0 expressed as 0.4 wt.% E SnO 1.1 wt.% 0.01 wt.% Li O 0.05 wt.%
- Example 7 An example for this is shown in Example 7 that follows.
- FIGS. 13 and 14 illustrate respectively improvements in the loss characteristics tan 8/11. and h of specimens of a ferrite having the same composition as in Example 1, i.e., MnOzZ- nOzFe o 38:61:55.9 mol percent and containing Li O and SnO as additive agents, the specimens being prepared, after sintering, by subjecting to a heat treatment for 32 hours at 250C.
- the manganese-zinc ferrites used in this example contained 0.06 wt. percent CaO and 0.02 wt. percent SiO besides SnO; and Li O.
- the effect of combined SnO and Li,0 per se was substantially unaffected when the amounts of addition of CaO and S10 were varied as will be evident from Example 8.
- F 10S. and 16 illustrate respectively graphs of tan Sly and h of manganese-zinc ferrites having a basic composition of 38.0 mol percent MnO, 6.1 mol percent ZnO, and 55.9 mol percent Fe,O and containing from 0 to 0.3 wt. percent CaO and from 0 to 0.04 wt. percent SiO
- FIGS. 17 and 18 illustrate respectively graphs of tan 6/11. and h of these ferrites which contained 0.05 wt. percent U 0 and 1.5 wt. percent SnO, as another additive combination.
- a preferred manganese-zinc ferrite composition consisting essentially of about 32.0 to 38.0 mol percent MnO, about 54.4 to 55.9 mol percent Fe O and the balance essentially ZnO, and containing about 0.01 to 0.1 weight percent Li O, about 0.4 to 3.2 weight percent $110,, less than about 0.3 weight percent CaO and less than about 0.04 weight percent S10
- a comparison of these graphs readily demonstrates that the effect of addition of SnO, and U 0 per se is still conspicuous under the co-presence of another additive combination C210 and SiO: in varying amounts.
- a manganese-zinc ferrite composition consisting essentially of about 28 to 40 mol percent MnO, about 51 to 58 mol percent Fe o and the balance essentially ZnO, and further containing less than about 0.3 percent by weight of calcium oxide, and, less than about 0.04 percent by weight of silicon and small but effective amounts of less than about 3.2 percent by weight of stannic oxide and less than about 0.125 percent weight of lithium oxide, said amounts of stannic oxide and lithium oxide being sufficient to effect improvements in the values of the quality factor (tan 6/;/.) and hysteresis loss factor (h of said composition, said ferrite composition being characterized by values of tan 8/;1. at KHz. of less than 1.3 l0' and h at 100 KHz. ofless than 5.
- composition containing about 0.01 to 0.1 weight percent Li O, about 0.4 to 3.2 weight percent SnO less than about 0.3 weight percent CaO and less than about 0.04 weight percent SiO, said composition being characterized by values of tan Sly. at KHz. ofless than 1.3X10 and h at 100 KHz. ofless than 5.0.
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- Engineering & Computer Science (AREA)
- Chemical & Material Sciences (AREA)
- Ceramic Engineering (AREA)
- Manufacturing & Machinery (AREA)
- Materials Engineering (AREA)
- Structural Engineering (AREA)
- Organic Chemistry (AREA)
- Magnetic Ceramics (AREA)
- Soft Magnetic Materials (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP7954068A JPS546713B1 (enrdf_load_stackoverflow) | 1968-10-30 | 1968-10-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3652416A true US3652416A (en) | 1972-03-28 |
Family
ID=13692816
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US872094A Expired - Lifetime US3652416A (en) | 1968-10-30 | 1969-10-29 | Oxide magnetic materials |
Country Status (6)
Country | Link |
---|---|
US (1) | US3652416A (enrdf_load_stackoverflow) |
JP (1) | JPS546713B1 (enrdf_load_stackoverflow) |
CA (1) | CA918906A (enrdf_load_stackoverflow) |
DE (1) | DE1953286B2 (enrdf_load_stackoverflow) |
FR (1) | FR2021906A1 (enrdf_load_stackoverflow) |
GB (1) | GB1271706A (enrdf_load_stackoverflow) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4372865A (en) * | 1980-09-26 | 1983-02-08 | Spang Industries, Inc. | Carbonate/hydroxide coprecipitation process |
US5518642A (en) * | 1992-01-14 | 1996-05-21 | Matsushita Electric Industrial Co., Ltd. | Oxide magnetic material |
US6858155B1 (en) | 2001-12-12 | 2005-02-22 | Spang & Company | Ferrite materials, methods of preparing the same, and products formed therefrom |
US20070181847A1 (en) * | 2006-02-08 | 2007-08-09 | Tdk Corporation | Ferrite material |
US20070267594A1 (en) * | 2006-05-17 | 2007-11-22 | Fanton Mark A | Ferrite materials, methods of preparing the same, and products formed therefrom |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS565046B1 (enrdf_load_stackoverflow) * | 1969-05-09 | 1981-02-03 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3415751A (en) * | 1964-11-27 | 1968-12-10 | Matsushita Electric Ind Co Ltd | Manganese-zinc ferrites |
US3492236A (en) * | 1963-07-26 | 1970-01-27 | Siemens Ag | Ferromagnetic core and process for its production |
-
1968
- 1968-10-30 JP JP7954068A patent/JPS546713B1/ja active Pending
-
1969
- 1969-10-23 GB GB52022/69A patent/GB1271706A/en not_active Expired
- 1969-10-23 DE DE19691953286 patent/DE1953286B2/de not_active Withdrawn
- 1969-10-28 FR FR6936982A patent/FR2021906A1/fr not_active Withdrawn
- 1969-10-29 CA CA066201A patent/CA918906A/en not_active Expired
- 1969-10-29 US US872094A patent/US3652416A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3492236A (en) * | 1963-07-26 | 1970-01-27 | Siemens Ag | Ferromagnetic core and process for its production |
US3415751A (en) * | 1964-11-27 | 1968-12-10 | Matsushita Electric Ind Co Ltd | Manganese-zinc ferrites |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4372865A (en) * | 1980-09-26 | 1983-02-08 | Spang Industries, Inc. | Carbonate/hydroxide coprecipitation process |
US5518642A (en) * | 1992-01-14 | 1996-05-21 | Matsushita Electric Industrial Co., Ltd. | Oxide magnetic material |
US6858155B1 (en) | 2001-12-12 | 2005-02-22 | Spang & Company | Ferrite materials, methods of preparing the same, and products formed therefrom |
US20070181847A1 (en) * | 2006-02-08 | 2007-08-09 | Tdk Corporation | Ferrite material |
US20070267594A1 (en) * | 2006-05-17 | 2007-11-22 | Fanton Mark A | Ferrite materials, methods of preparing the same, and products formed therefrom |
Also Published As
Publication number | Publication date |
---|---|
FR2021906A1 (enrdf_load_stackoverflow) | 1970-07-24 |
DE1953286A1 (de) | 1970-05-14 |
JPS546713B1 (enrdf_load_stackoverflow) | 1979-03-30 |
DE1953286B2 (de) | 1972-12-07 |
GB1271706A (en) | 1972-04-26 |
CA918906A (en) | 1973-01-16 |
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