JPH08151258A - Oxide magnetic material - Google Patents

Oxide magnetic material

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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
Authority
JP
Japan
Prior art keywords
mol
magnetic material
oxide magnetic
converted
reducing
Prior art date
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.)
Granted
Application number
JP6317651A
Other languages
Japanese (ja)
Other versions
JP3167561B2 (en
Inventor
Yasushi Inoue
泰史 井上
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Taiyo Yuden Co Ltd
Original Assignee
Taiyo Yuden Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Taiyo Yuden Co Ltd filed Critical Taiyo Yuden Co Ltd
Priority to JP31765194A priority Critical patent/JP3167561B2/en
Publication of JPH08151258A publication Critical patent/JPH08151258A/en
Application granted granted Critical
Publication of JP3167561B2 publication Critical patent/JP3167561B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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  • Magnetic Ceramics (AREA)
  • Soft Magnetic Materials (AREA)

Abstract

PURPOSE: To obtain an oxide magnetic material having high magnetic permeability and making usable of Ag, Ag-Pd or Ag-Cu, etc., as an inner conductor. CONSTITUTION: This magnetic material contains Fe in an amount of 45.0-50.0mol% reducing to Fe2 O3 , Ni in an amount of 15.0-30.0mol% reducing to NiO, Cu in an amount of 8.0-15.0mol% reducing to CuO, Zn in an amount of 15.0-25.0mol% reducing to ZnO, at least a metal selected from Mg, Ca, Sr, Ba, Mo, W, V and Cr in the total of 0.1-3.0mol% respectively reducing to MgO, CaO, SrO, BaO, MoO, WO, V2 O5 , and Cr2 O3 , and Li in an amount of 0.01-3.0mol% reducing to Li2 O.

Description

【発明の詳細な説明】Detailed Description of the Invention

【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Fe23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、V25、Cr23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、V25、Cr23、Mn34 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。Fe23、NiO、CuO、ZnO、
MgO、CaO、SrO、BaO、MoO、WO、V2
5、Cr23及び/又はMn34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。Fe23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、V25及びCr23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、V25、Cr23及びMn34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)

【特許請求の範囲】[Claims] 【請求項1】 FeをFe23に換算して45.0〜5
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
25、Cr23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%.
【請求項2】 950℃以下の温度で焼成されたもので
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.
【請求項3】 FeをFe23に換算して45.0〜5
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、V25、Cr23、Mn34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.
【請求項4】 950℃以下の温度で焼成されたもので
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.
JP31765194A 1994-11-28 1994-11-28 Oxide magnetic material Expired - Fee Related JP3167561B2 (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (5)

* Cited by examiner, † Cited by third party
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

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JP3167561B2 (en) 2001-05-21

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