JPH08151258A - Oxide magnetic material - Google Patents
Oxide magnetic materialInfo
- Publication number
- JPH08151258A JPH08151258A JP6317651A JP31765194A JPH08151258A JP H08151258 A JPH08151258 A JP H08151258A JP 6317651 A JP6317651 A JP 6317651A JP 31765194 A JP31765194 A JP 31765194A JP H08151258 A JPH08151258 A JP H08151258A
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- JP
- Japan
- Prior art keywords
- mol
- magnetic material
- oxide magnetic
- converted
- reducing
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- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
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- Magnetic Ceramics (AREA)
- Soft Magnetic Materials (AREA)
Abstract
Description
【0001】[0001]
【産業上の利用分野】本発明は、インダクタ等の電気部
品に使用される酸化物磁性材料に関する。BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to an oxide magnetic material used for electric parts such as inductors.
【0002】[0002]
【従来の技術】インダクタ等の電気部品に使用される酸
化物磁性材料としてNi−Cu−Zn系フェライト酸化
物磁性材料が知られている。例えば、特開昭50−10
7008号には、Ni−Cu−Zn系の高抵抗率低損失
酸化物磁性材料が開示されている。2. Description of the Related Art Ni-Cu-Zn type ferrite oxide magnetic material is known as an oxide magnetic material used for electric parts such as inductors. For example, JP-A-50-10
No. 7008 discloses a Ni—Cu—Zn-based high resistivity, low loss oxide magnetic material.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、従来の
Ni−Cu−Zn系酸化物磁性材料を使用した場合、チ
ップ等の形状が小さくなると、満足できる透磁率を得る
ことは難しい。また、焼成温度が1000℃以上と比較
的高いため、内部導体としてAg、Ag−Pd、Ag−
Cu等の融点が1000℃より低い金属導体を使用する
ことが不可能であった。そこで、本発明の目的は、高い
透磁率を有する酸化物磁性材料であって、内部導体とし
てAg、Ag−Pd、Ag−Cu等の金属導体の使用を
可能にした材料を提供することである。However, when the conventional Ni-Cu-Zn-based oxide magnetic material is used, it is difficult to obtain a satisfactory magnetic permeability when the shape of the chip or the like becomes small. Moreover, since the firing temperature is relatively high at 1000 ° C. or higher, Ag, Ag—Pd, Ag—
It was impossible to use a metal conductor such as Cu having a melting point lower than 1000 ° C. Therefore, an object of the present invention is to provide an oxide magnetic material having a high magnetic permeability, which enables use of a metal conductor such as Ag, Ag-Pd, or Ag-Cu as an inner conductor. .
【0004】[0004]
【課題を解決するための手段】本発明の酸化物磁性材料
は、上記目的を達成すべく、FeをFe2O3に換算して
45.0〜50.0mol%、NiをNiOに換算して
15.0〜30.0mol%、CuをCuOに換算して
8.0〜15.0mol%、ZnをZnOに換算して1
5.0〜25.0mol%、Mg、Ca、Sr、Ba,
Mo、W、V及びCrから選ばれる少なくとも一種の金
属をそれぞれMgO、CaO、SrO、BaO、Mo
O、WO、V2O5、Cr2O3に換算して合計で0.1〜
3.0mol%及びLiをLi2O に換算して0.01
〜3.0mol%含むことを特徴とする。かかる酸化物
磁性材料は950℃以下の温度で焼成され得る。また、
上記酸化物磁性材料において、Mg、Ca、Sr、B
a,Mo、W、V及びCrから選ばれる少なくとも一種
の金属の代わりに、Mg、Ca、Sr、Ba,Mo、
W、V及びCrから選ばれる少なくとも一種の金属とM
nとをそれぞれMgO、CaO、SrO、BaO、Mo
O、WO、V2O5、Cr2O3、Mn3O4 に換算して合
計で0.1〜3.0mol%含ませることが好ましい。
この酸化物磁性材料も950℃以下の温度で焼成され得
る。In order to achieve the above-mentioned object, the oxide magnetic material of the present invention has Fe converted to Fe 2 O 3 of 45.0 to 50.0 mol% and Ni converted to NiO. 15.0 to 30.0 mol%, Cu to CuO is 8.0 to 15.0 mol%, and Zn is to ZnO to be 1
5.0-25.0 mol%, Mg, Ca, Sr, Ba,
At least one metal selected from Mo, W, V and Cr is MgO, CaO, SrO, BaO and Mo, respectively.
O, 0.1 to a total in terms WO, the V 2 O 5, Cr 2 O 3
3.0 mol% and 0.01 in terms of Li converted to Li 2 O
It is characterized by containing ~ 3.0 mol%. Such oxide magnetic materials can be fired at temperatures below 950 ° C. Also,
In the above oxide magnetic material, Mg, Ca, Sr, B
Instead of at least one metal selected from a, Mo, W, V and Cr, Mg, Ca, Sr, Ba, Mo,
At least one metal selected from W, V and Cr and M
n and MgO, CaO, SrO, BaO, Mo respectively
O, WO, V 2 O 5 , Cr 2 O 3, Mn preferably be contained 0.1~3.0Mol% in total in terms of the 3 O 4.
This oxide magnetic material can also be fired at temperatures below 950 ° C.
【0005】[0005]
【作用】本発明の酸化物磁性材料によれば、比抵抗を低
下させることなく、透磁率を向上させることができる。
即ち、比抵抗1000MΩ・cm以上且つ透磁率250
以上を有する酸化物磁性材料が得られる。また、950
℃以下での焼成が可能となり、内部導体にAg、Ag−
Pd、Ag−Cu等を使用することができる。According to the oxide magnetic material of the present invention, the magnetic permeability can be improved without lowering the specific resistance.
That is, the specific resistance is 1000 MΩ · cm or more and the magnetic permeability is 250.
An oxide magnetic material having the above is obtained. Also, 950
Baking at below ℃ becomes possible, and Ag, Ag-
Pd, Ag-Cu, etc. can be used.
【0006】[0006]
【実施例】以下、本発明を実施例及び比較例に基づいて
詳細に説明する。Fe2O3、NiO、CuO、ZnO、
MgO、CaO、SrO、BaO、MoO、WO、V2
O5、Cr2O3及び/又はMn3O4並びに焼き上がりで
0.01〜3.0mol%のLi2O に相当するLiC
lを、それぞれ表1〜3に示す割合で秤量し、湿式混合
後、脱水、乾燥した。この乾燥物を大気中で約700〜
約800℃の範囲の温度で1時間仮焼し、その後ボール
ミルで15時間解砕した。これに有機バインダを加え
て、造粒、成型し、大気中で約850〜約950℃の範
囲の温度で1時間焼成した。かくして得られた燒結体の
透磁率μ及び比抵抗ρを測定した。なお、透磁率は周波
数100MHz、電圧0.5Vの条件でまた比抵抗は電
圧25V、保持時間20秒の条件で測定した。得られた
結果を表1〜3に示す。なお、表1〜3中の試料No.
に*印があるものは本発明の組成範囲外のもので、比較
例である。EXAMPLES The present invention will be described in detail below based on examples and comparative examples. Fe 2 O 3 , NiO, CuO, ZnO,
MgO, CaO, SrO, BaO, MoO, WO, V 2
O 5 , Cr 2 O 3 and / or Mn 3 O 4 and LiC corresponding to 0.01 to 3.0 mol% of Li 2 O after baking
1 was weighed in the proportions shown in Tables 1 to 3, wet-mixed, dehydrated and dried. Approximately 700-
It was calcined at a temperature in the range of about 800 ° C. for 1 hour and then crushed by a ball mill for 15 hours. An organic binder was added to this, and the mixture was granulated, molded, and fired in the atmosphere at a temperature in the range of about 850 to about 950 ° C for 1 hour. The magnetic permeability μ and the specific resistance ρ of the sintered body thus obtained were measured. The magnetic permeability was measured at a frequency of 100 MHz and a voltage of 0.5 V, and the specific resistance was measured at a voltage of 25 V and a holding time of 20 seconds. The obtained results are shown in Tables 1-3. In addition, sample No. 1 in Tables 1-3.
Those marked with * are outside the composition range of the present invention and are comparative examples.
【0007】[0007]
【表1】 [Table 1]
【0008】[0008]
【表2】 [Table 2]
【0009】[0009]
【表3】 [Table 3]
【0010】表1〜3から明らかなように、本発明で特
定された組成範囲内の酸化物磁性材料は、透磁率μが2
50以上且つ比抵抗ρが1000MΩ・cm以上の特性
を有している。また、950℃以下での焼成が可能であ
る。一方、本発明の範囲外の組成範囲を有する酸化物磁
性材料では、上記したような所望特性を得ることができ
ない。As is clear from Tables 1 to 3, the oxide magnetic materials within the composition range specified in the present invention have a magnetic permeability μ of 2 or less.
It has a characteristic of 50 or more and a specific resistance ρ of 1000 MΩ · cm or more. Also, firing at 950 ° C. or lower is possible. On the other hand, an oxide magnetic material having a composition range outside the range of the present invention cannot obtain the above-mentioned desired characteristics.
【0011】表1〜3に示された結果に基づいて各成分
の組成範囲の限定理由を説明する。Fe2O3について
は、45.0mol%未満だと透磁率及び比抵抗が共に
低く(試料No.1)、50.0mol%を越えると9
00℃では燒結しない(試料No.5)。NiOについ
ては、15.0mol%未満だと比抵抗が低く(試料N
o.6)、30.0mol%を越えると透磁率が低い
(試料No.9)。CuOについては、8.0mol%
未満だと900℃では燒結せず(試料No.10)、1
5.0mol%を越えると透磁率及び比抵抗が共に低い
(試料No.11)。ZnOについては、15.0mo
l%未満だと透磁率及び比抵抗が共に低く(試料No.
12)、25.0mol%を越えると比抵抗が低い(試
料No.15)。MgO、CaO、SrO、BaO、M
oO、WO、V2O5及びCr2O3については、それらの
和が0.1mol%未満だと透磁率が低く(試料No.
16)、3.0mol%を越えると比抵抗が低いか又は
900℃では燒結しない(試料No.19、49〜5
5)。Li2O については、0.01mol%未満だと
900℃では燒結せず(試料No.20)、3.0mo
l%を越えると比抵抗が低い(試料No.23)。The reason for limiting the composition range of each component will be described based on the results shown in Tables 1 to 3. Regarding Fe 2 O 3, if it is less than 45.0 mol%, both the magnetic permeability and the specific resistance are low (Sample No. 1), and if it exceeds 50.0 mol%, it is 9
It does not sinter at 00 ° C (Sample No. 5). Regarding NiO, if it is less than 15.0 mol%, the specific resistance is low (Sample N
o. 6) If it exceeds 30.0 mol%, the magnetic permeability is low (Sample No. 9). For CuO, 8.0 mol%
If it is less than 900 ° C, it does not sinter at 900 ° C (Sample No. 10), 1
When it exceeds 5.0 mol%, both the magnetic permeability and the specific resistance are low (Sample No. 11). For ZnO, 15.0mo
If it is less than 1%, both the magnetic permeability and the specific resistance are low (Sample No.
12) If it exceeds 25.0 mol%, the specific resistance is low (Sample No. 15). MgO, CaO, SrO, BaO, M
Regarding oO, WO, V 2 O 5 and Cr 2 O 3 , if the sum of them is less than 0.1 mol%, the magnetic permeability is low (Sample No.
16), if it exceeds 3.0 mol%, the specific resistance is low or it does not sinter at 900 ° C. (Sample No. 19, 49 to 5).
5). Regarding Li 2 O, if it is less than 0.01 mol%, it does not sinter at 900 ° C. (Sample No. 20), and 3.0 mo
If it exceeds 1%, the specific resistance is low (Sample No. 23).
【0012】また、MgO、CaO、SrO、BaO、
MoO、WO、V2O5、Cr2O3及びMn3O4の和が
0.1mol%未満だと透磁率が低く(試料No.1
6)、3.0mol%を越えると900℃では燒結しな
い(試料No.56、57)。なお、上記実施例及び比
較例では、Li酸化物は配合時LiClとして用いた
が、これに限定されるものではなく、例えば、Li
2O、Li2CO3 、Li有機酸塩等も用いることができ
る。また、他の金属の場合は、原料として、例えば、そ
の酸化物又は炭酸塩が使用されうる。Further, MgO, CaO, SrO, BaO,
If the sum of MoO, WO, V 2 O 5 , Cr 2 O 3 and Mn 3 O 4 is less than 0.1 mol%, the magnetic permeability is low (Sample No. 1).
6), if it exceeds 3.0 mol%, it does not sinter at 900 ° C. (Sample Nos. 56 and 57). Although Li oxide was used as LiCl at the time of compounding in the above-mentioned Examples and Comparative Examples, it is not limited to this and, for example, Li
2 O, Li 2 CO 3 , Li organic acid salts and the like can also be used. Further, in the case of other metals, for example, its oxide or carbonate can be used as a raw material.
【0013】[0013]
【発明の効果】以上詳細に説明したように、本発明によ
れば、酸化物磁性材料の構成成分の組成割合を適宜選ぶ
ことにより、比抵抗1000MΩ・cm以上且つ透磁率
250以上を有する酸化物磁性材料が得られる。950
℃以下の温度で焼成可能であるので、内部導体としてA
g等の低融点金属導体の使用を可能にし、産業上極めて
有益である。As described above in detail, according to the present invention, an oxide having a specific resistance of 1000 MΩ · cm or more and a magnetic permeability of 250 or more can be obtained by appropriately selecting the composition ratio of the constituent components of the oxide magnetic material. A magnetic material is obtained. 950
Since it can be fired at a temperature below ℃,
It enables the use of low melting point metal conductors such as g, which is extremely useful in industry.
───────────────────────────────────────────────────── フロントページの続き (51)Int.Cl.6 識別記号 庁内整理番号 FI 技術表示箇所 H01F 1/34 ─────────────────────────────────────────────────── ─── Continuation of the front page (51) Int.Cl. 6 Identification code Internal reference number FI technical display H01F 1/34
Claims (4)
0.0mol%、NiをNiOに換算して15.0〜3
0.0mol%、CuをCuOに換算して8.0〜1
5.0mol%、ZnをZnOに換算して15.0〜2
5.0mol%、Mg、Ca、Sr、Ba、Mo、W、
V及びCrから選ばれる少なくとも一種の金属をそれぞ
れMgO、CaO、SrO、BaO、MoO、WO、V
2O5、Cr2O3に換算して合計で0.1〜3.0mol
%並びにLiをLi2O に換算して0.01〜3.0m
ol%含むことを特徴とする酸化物磁性材料。1. Fe is converted to Fe 2 O 3 and it is 45.0-5.
0.0 mol%, Ni converted to NiO, 15.0 to 3
0.0 mol%, Cu converted to CuO 8.0-1
5.0 mol%, Zn converted to ZnO, 15.0 to 2
5.0 mol%, Mg, Ca, Sr, Ba, Mo, W,
MgO, CaO, SrO, BaO, MoO, WO, and V each containing at least one metal selected from V and Cr.
Converted to 2 O 5 and Cr 2 O 3 , 0.1 to 3.0 mol in total
% And Li converted to Li 2 O, 0.01 to 3.0 m
An oxide magnetic material characterized by containing ol%.
あることを特徴とする請求項1記載の酸化物磁性材料。2. The oxide magnetic material according to claim 1, which is fired at a temperature of 950 ° C. or lower.
0.0mol%、NiをNiOに換算して15.0〜3
0.0mol%、CuをCuOに換算して8.0〜1
5.0mol%、ZnをZnOに換算して15.0〜2
5.0mol%、Mg、Ca、Sr、Ba,Mo、W、
V及びCrから選ばれる少なくとも一種の金属とMnと
をそれぞれMgO、CaO、SrO、BaO、MoO、
WO、V2O5、Cr2O3、Mn3O4に換算して合計で
0.1〜3.0mol%並びにLiをLi2O に換算し
て0.01〜3.0mol%含むことを特徴とする酸化
物磁性材料。3. Fe is converted to Fe 2 O 3 and 45.0 to 5
0.0 mol%, Ni converted to NiO, 15.0 to 3
0.0 mol%, Cu converted to CuO 8.0-1
5.0 mol%, Zn converted to ZnO, 15.0 to 2
5.0 mol%, Mg, Ca, Sr, Ba, Mo, W,
At least one metal selected from V and Cr and Mn are MgO, CaO, SrO, BaO, MoO, and
WO, V 2 O 5, Cr 2 O 3, Mn 3 O 4 include 0.01~3.0Mol% of 0.1~3.0Mol% and Li in total in terms in terms of Li 2 O to An oxide magnetic material characterized by.
あることを特徴とする請求項3記載の酸化物磁性材料。4. The oxide magnetic material according to claim 3, which is fired at a temperature of 950 ° C. or lower.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31765194A JP3167561B2 (en) | 1994-11-28 | 1994-11-28 | Oxide magnetic material |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP31765194A JP3167561B2 (en) | 1994-11-28 | 1994-11-28 | Oxide magnetic material |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH08151258A true JPH08151258A (en) | 1996-06-11 |
JP3167561B2 JP3167561B2 (en) | 2001-05-21 |
Family
ID=18090526
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP31765194A Expired - Fee Related JP3167561B2 (en) | 1994-11-28 | 1994-11-28 | Oxide magnetic material |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP3167561B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1231614A1 (en) * | 2001-02-13 | 2002-08-14 | TDK Corporation | Oxide magnetic material and core using the same |
US6583699B2 (en) * | 2000-10-31 | 2003-06-24 | Tdk Corporation | Magnetic material and inductor |
WO2010113772A1 (en) * | 2009-03-30 | 2010-10-07 | 双信電機株式会社 | Ferrite material and electronic component |
-
1994
- 1994-11-28 JP JP31765194A patent/JP3167561B2/en not_active Expired - Fee Related
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6583699B2 (en) * | 2000-10-31 | 2003-06-24 | Tdk Corporation | Magnetic material and inductor |
EP1231614A1 (en) * | 2001-02-13 | 2002-08-14 | TDK Corporation | Oxide magnetic material and core using the same |
WO2010113772A1 (en) * | 2009-03-30 | 2010-10-07 | 双信電機株式会社 | Ferrite material and electronic component |
JP2010235328A (en) * | 2009-03-30 | 2010-10-21 | Soshin Electric Co Ltd | Ferrite material and electronic component |
US8562851B2 (en) | 2009-03-30 | 2013-10-22 | Soshin Electric Co., Ltd. | Ferrite material and electronic component |
Also Published As
Publication number | Publication date |
---|---|
JP3167561B2 (en) | 2001-05-21 |
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