JPH03163803A - Low loss mn-zn system ferrite - Google Patents
Low loss mn-zn system ferriteInfo
- Publication number
- JPH03163803A JPH03163803A JP1301880A JP30188089A JPH03163803A JP H03163803 A JPH03163803 A JP H03163803A JP 1301880 A JP1301880 A JP 1301880A JP 30188089 A JP30188089 A JP 30188089A JP H03163803 A JPH03163803 A JP H03163803A
- Authority
- JP
- Japan
- Prior art keywords
- loss
- transformer
- mno
- power supply
- zno
- 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
Links
- 229910000859 α-Fe Inorganic materials 0.000 title claims description 5
- 229910000484 niobium oxide Inorganic materials 0.000 claims abstract description 8
- URLJKFSTXLNXLG-UHFFFAOYSA-N niobium(5+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[O-2].[Nb+5].[Nb+5] URLJKFSTXLNXLG-UHFFFAOYSA-N 0.000 claims abstract description 8
- 229910000476 molybdenum oxide Inorganic materials 0.000 claims abstract description 5
- QGLKJKCYBOYXKC-UHFFFAOYSA-N nonaoxidotritungsten Chemical compound O=[W]1(=O)O[W](=O)(=O)O[W](=O)(=O)O1 QGLKJKCYBOYXKC-UHFFFAOYSA-N 0.000 claims abstract description 5
- PQQKPALAQIIWST-UHFFFAOYSA-N oxomolybdenum Chemical compound [Mo]=O PQQKPALAQIIWST-UHFFFAOYSA-N 0.000 claims abstract description 5
- 229910001930 tungsten oxide Inorganic materials 0.000 claims abstract description 5
- 238000002156 mixing Methods 0.000 claims description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 abstract description 16
- 229910052742 iron Inorganic materials 0.000 abstract description 8
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 abstract description 7
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 abstract description 5
- 229910052681 coesite Inorganic materials 0.000 abstract description 4
- 150000001875 compounds Chemical class 0.000 abstract description 4
- 229910052906 cristobalite Inorganic materials 0.000 abstract description 4
- 229910052682 stishovite Inorganic materials 0.000 abstract description 4
- 229910052905 tridymite Inorganic materials 0.000 abstract description 4
- 239000000377 silicon dioxide Substances 0.000 abstract description 3
- 235000012239 silicon dioxide Nutrition 0.000 abstract description 3
- 238000013329 compounding Methods 0.000 abstract 1
- 235000013339 cereals Nutrition 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- 239000011701 zinc Substances 0.000 description 6
- 230000005291 magnetic effect Effects 0.000 description 5
- 230000002159 abnormal effect Effects 0.000 description 4
- 239000002994 raw material Substances 0.000 description 4
- 238000001354 calcination Methods 0.000 description 2
- 239000013078 crystal Substances 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000005245 sintering Methods 0.000 description 2
- -1 M003) Chemical compound 0.000 description 1
- 240000007594 Oryza sativa Species 0.000 description 1
- 235000007164 Oryza sativa Nutrition 0.000 description 1
- 229910001035 Soft ferrite Inorganic materials 0.000 description 1
- FMRLDPWIRHBCCC-UHFFFAOYSA-L Zinc carbonate Chemical compound [Zn+2].[O-]C([O-])=O FMRLDPWIRHBCCC-UHFFFAOYSA-L 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- WUKWITHWXAAZEY-UHFFFAOYSA-L calcium difluoride Chemical compound [F-].[F-].[Ca+2] WUKWITHWXAAZEY-UHFFFAOYSA-L 0.000 description 1
- 238000002485 combustion reaction Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- VEPSWGHMGZQCIN-UHFFFAOYSA-H ferric oxalate Chemical compound [Fe+3].[Fe+3].[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O.[O-]C(=O)C([O-])=O VEPSWGHMGZQCIN-UHFFFAOYSA-H 0.000 description 1
- 238000010304 firing Methods 0.000 description 1
- 239000010436 fluorite Substances 0.000 description 1
- 230000004907 flux Effects 0.000 description 1
- 235000014413 iron hydroxide Nutrition 0.000 description 1
- NCNCGGDMXMBVIA-UHFFFAOYSA-L iron(ii) hydroxide Chemical compound [OH-].[OH-].[Fe+2] NCNCGGDMXMBVIA-UHFFFAOYSA-L 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
- RGVLTEMOWXGQOS-UHFFFAOYSA-L manganese(2+);oxalate Chemical compound [Mn+2].[O-]C(=O)C([O-])=O RGVLTEMOWXGQOS-UHFFFAOYSA-L 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
- 239000000463 material Substances 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 230000003647 oxidation Effects 0.000 description 1
- 238000007254 oxidation reaction Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000000700 radioactive tracer Substances 0.000 description 1
- 235000009566 rice Nutrition 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- 235000004416 zinc carbonate Nutrition 0.000 description 1
- 239000011667 zinc carbonate Substances 0.000 description 1
- 229910000010 zinc carbonate Inorganic materials 0.000 description 1
- ZPEJZWGMHAKWNL-UHFFFAOYSA-L zinc;oxalate Chemical compound [Zn+2].[O-]C(=O)C([O-])=O ZPEJZWGMHAKWNL-UHFFFAOYSA-L 0.000 description 1
Landscapes
- Compounds Of Iron (AREA)
- Magnetic Ceramics (AREA)
- Soft Magnetic Materials (AREA)
Abstract
Description
【発明の詳細な説明】
(産業上の利用分野)
この発明は、スイッチング電源用トランス等の用途に供
して好適な低損失Mn−Zn系フエライトに関するもの
である。DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to a low-loss Mn-Zn ferrite suitable for use in transformers for switching power supplies and the like.
?従来の技術)
従来、スイッチング電源用トランスは、スイッチング周
波数: 100 kHz程度で使用されることが多かっ
たが、最近、電源の高性能化、小型化のために、高周波
数化さらにはそれに伴うコアの一層の低鉄損化が望まれ
ている。? Conventional technology) Conventionally, transformers for switching power supplies were often used at a switching frequency of about 100 kHz, but recently, in order to improve the performance and downsize of power supplies, the frequency has increased and the core Further reduction of iron loss is desired.
このような観点から、かかるトランス材として使用され
るMn−Znフヱライトについても、電磁特1生改善の
ために種々の微量或分の添加が試みられている。たとえ
ば特開昭61−101458号公報にはCaOとSiO
■との複合添加が、また特開昭58−15037号公報
には酸化ニオブの添加がそれぞれ提案されている。From this point of view, attempts have been made to add various trace amounts of Mn--Zn fluorite used as such transformer materials in order to improve electromagnetic properties. For example, in Japanese Patent Application Laid-open No. 101458/1983, CaO and SiO
A composite addition of niobium oxide and niobium oxide is proposed in Japanese Unexamined Patent Publication No. 58-15037.
(発明が解決しようとする課題)
しかしながらCaOやSiO■を添加すると結晶粒が異
常威長を起す場合があり、磁気特性劣化の原因となって
いた。(Problems to be Solved by the Invention) However, when CaO or SiO2 is added, crystal grains may become abnormally elongated, causing deterioration of magnetic properties.
すなわち異常戒長じた結晶粒内には多くの空孔が残留す
るため、この空孔に起因して透磁率や鉄損などの低下を
招いていたのである。In other words, many vacancies remain in the abnormally elongated crystal grains, which causes a decrease in magnetic permeability, iron loss, etc.
この発明は、上記の問題を有利に解決するもので、10
0 kHz以上の高周波スイッチング電源用1・ランス
として使用した場合においても、損失を−F分低く抑制
して、その高性能化、小型化を実現できる低損失Mn
− Zn系フエライトを提案することを目的とする。This invention advantageously solves the above problems, and has 10
Even when used as a lance for high-frequency switching power supplies of 0 kHz or higher, the loss can be suppressed by -F to achieve higher performance and smaller size.
- The purpose is to propose Zn-based ferrite.
(課題を解決するための手段)
すなわちこの発明は、
Pez[:+ : 52−54mol%、MnO :
33〜37mol%およびZnO:8〜13moI%
を基本成分とし、この基本成分に
Si(h : 0.008〜0.030wt%、CaO
: 0.02〜0.15wt%と、
酸化ニオブ: 0.01〜0.08wt%、酸化タング
ステン及び/又は酸化モリブデン: 0.02〜0.2
0wt%
とを添加配合してなる低損失Mn − Zn系フエライ
トである。(Means for Solving the Problems) That is, the present invention provides: Pez[:+: 52-54 mol%, MnO:
33 to 37 mol% and ZnO: 8 to 13 mol% as basic components, and Si (h: 0.008 to 0.030 wt%, CaO
: 0.02 to 0.15 wt%, Niobium oxide: 0.01 to 0.08 wt%, Tungsten oxide and/or molybdenum oxide: 0.02 to 0.2
This is a low loss Mn-Zn based ferrite made by adding and blending 0wt%.
(作 用)
まずこの発明において、基本成分の配合割合を上記の範
囲に限定した理由について説明する。(Function) First, in this invention, the reason why the blending ratio of the basic components is limited to the above range will be explained.
Fe203: 52〜54mol%、MnO : 33
〜37mol%、ZnO : 8 〜13mol%
スイッチング電源用トランスの動作温度は、通常60〜
70゜Cであり、従ってこの温度範囲で銖損が低く、か
つ室温から動作温度を超える80〜120゜C程度の温
度域まで鉄損が負の温度依存性をもつことが望ましい。Fe203: 52-54 mol%, MnO: 33
~37 mol%, ZnO: 8 ~ 13 mol% The operating temperature of a switching power supply transformer is usually 60 ~
70 DEG C. Therefore, it is desirable that the iron loss is low in this temperature range, and that the iron loss has a negative temperature dependence from room temperature to a temperature range of about 80 DEG to 120 DEG C., which exceeds the operating temperature.
この観点からFe20,,. MnO, ZnOの配合
割合を検討した結果、上記の範囲が得られたのである。From this point of view, Fe20,... As a result of examining the blending ratios of MnO and ZnO, the above range was obtained.
なおFe203原料としては、p e2 0 3だ6ノ
でな<、FeOやFe304、さらには焼威によりFe
203に変わることのできる化合物、例えば水酸化鉄、
しゅう酸化鉄などを使用することができる。またMnO
原料としては、MnOのみならず、MnOz, Mns
O4さらには焼或によりMnOに変わることのできる化
合物、例えば炭酸マンガン、しゅう酸マンガンなどを使
用することができる。さらにZnO原料としては、Zn
Oのみ?限らず、焼或によりZnOに変わることのでき
る化合物、例えば炭酸亜鉛、しゅう酸亜鉛などを使用す
ることができる。In addition, Fe203 raw materials include p e2 0 3 to 6 <, FeO, Fe304, and even Fe203 due to combustion.
Compounds that can be converted into 203, such as iron hydroxide,
Iron oxalate, etc. can be used. Also, MnO
As a raw material, not only MnO but also MnOz, Mns
Compounds that can be converted to MnO by calcination or oxidation, such as manganese carbonate, manganese oxalate, etc., can be used. Furthermore, as a ZnO raw material, Zn
Only O? However, compounds that can be converted into ZnO by calcination, such as zinc carbonate, zinc oxalate, etc., can be used.
SiOz : 0.008〜0.030wt%SiO■
は、CaOとの共存によって粒界の比抵抗を高め、渦電
流損の低減に有効に寄与するが、含有量が0.008w
t%に満たないとその添加効果に乏しく、一方0.03
0wL%を超えると焼或時に異常粒威長が起り易く特性
が不安定になるので、0.008〜0.03kt%の範
囲に限定した。SiOz: 0.008~0.030wt%SiO■
coexists with CaO to increase the specific resistance of grain boundaries and effectively contribute to reducing eddy current loss, but when the content is 0.008w
If the amount is less than t%, the effect of addition is poor; on the other hand, 0.03
If it exceeds 0 wL%, abnormal grain length tends to occur during firing and the properties become unstable, so it was limited to a range of 0.008 to 0.03 kt%.
CaO : 0.02〜0.15wt%CaOは、粒界
抵抗を高めると共に、結晶粒を微細化して低鉄損をもた
らす有用成分であるが、含有量が0.02wt%に満た
ないと粒界抵抗の向上効果に乏しく、一方0.15wt
%を超えると、密度を高くするために高温で焼結した場
合に異常粒或長を起こし易くなるので、0.02〜0.
15wt%の範囲で添加するものとした。CaO: 0.02 to 0.15 wt% CaO is a useful component that increases grain boundary resistance and refines grains, resulting in low core loss. However, if the content is less than 0.02 wt%, grain boundary Poor resistance improvement effect, on the other hand, 0.15wt
If it exceeds 0.02 to 0.0%, abnormal grain length tends to occur when sintering at high temperature to increase density.
It was supposed to be added in a range of 15 wt%.
酸化二オブ: 0.01〜0.08wt%酸化ニオブ(
主にNb205)の添加によって鉄損5
特性が改善される理由は明らかでないが、SiO2、C
aOとの複合添加によって粒界の高抵抗相を変質させ、
比抵抗を増加させると共に、異質の相が粒界に存在する
ことによる磁気的な悪影響を緩和する働きがあるためと
考えられる。しかしながら含有量が0.01wt%に満
たないとその添加効果に乏しく、一方0 . 08w
t%を超えて含有されると焼結時に異常粒或長を起こし
易くなるので、0.Ol〜0.08wt%の範囲で添加
するものとした。Niobium oxide: 0.01-0.08wt% niobium oxide (
Although it is not clear why the core loss5 characteristics are improved mainly by the addition of Nb205), SiO2, C
The high-resistance phase at the grain boundaries is altered by combined addition with aO,
This is thought to be because it not only increases resistivity but also works to alleviate the negative magnetic effects caused by the presence of foreign phases at grain boundaries. However, if the content is less than 0.01 wt%, the effect of its addition is poor; 08w
If the content exceeds t%, abnormal grain length tends to occur during sintering, so 0. It was supposed to be added in a range of 0.08 wt%.
酸化タングステン及び/又は酸化モリブデン:0.02
〜0 . 20w t%
酸化タングステン(主に問.)及び/又は酸化モリブデ
ン(主にM003)を、Si02,CaOおよびNb2
05などと複合して添加することによって、一層銖損が
改善される。その理由は明確でないが、上述した酸化二
オブと同様な効果によるものと考えられる。これらの元
素は各々単独でも両者同時に添加してもよいが、0 .
02w t%未満の添加効果に乏しく、一方0.2w
t%を超えて多量に添加するとかえって磁気特性は劣化
するので、これらの成分は単独使6
用、併用いずれの場合においても、0.02〜0.20
wt%の範囲で添加するものとした。Tungsten oxide and/or molybdenum oxide: 0.02
~0. 20wt% tungsten oxide (mainly Q.) and/or molybdenum oxide (mainly M003), Si02, CaO and Nb2
By adding it in combination with 05 or the like, the corrosion loss can be further improved. The reason for this is not clear, but it is thought to be due to the same effect as that of niobium oxide mentioned above. Each of these elements may be added alone or both may be added at the same time.
Addition effects of less than 0.2w t% are poor, while 0.2w
If added in large amounts exceeding t%, the magnetic properties will deteriorate, so these components should be added in amounts of 0.02 to 0.20 whether used alone or in combination.
It was supposed to be added in a range of wt%.
(実施例)
Fe20: 52.7 mol%, MnO : 34
.5 mol%およびZnO: 12.8 mol%か
らなる基本組威の原料を混合したのち、大気中にて90
0゜C、3時間仮焼した。この仮焼粉に対し、表1に示
す割合でSiO。, Cab, NbzOsWO.およ
びMo03を添加配合し、同時に湿式ボールミルで粉砕
、混合した。ついで籾砕粉にバインダーとしてPVAを
添加し、造粒した後、外径36mm、内径24mm、高
さ12mmのリング状に或形したのち、酸素濃度を制御
した雰囲気中で1320゜C、3時間の焼威を行った。(Example) Fe20: 52.7 mol%, MnO: 34
.. 5 mol% and ZnO: After mixing the raw materials with a basic composition consisting of 12.8 mol%,
It was calcined at 0°C for 3 hours. SiO was added to this calcined powder in the proportions shown in Table 1. , Cab, NbzOsWO. and Mo03 were added and blended, and simultaneously ground and mixed using a wet ball mill. Next, PVA was added as a binder to the crushed rice powder, and after granulating it, it was shaped into a ring shape with an outer diameter of 36 mm, an inner diameter of 24 mm, and a height of 12 mm, and then heated at 1320 ° C for 3 hours in an atmosphere with a controlled oxygen concentration. The fire was carried out.
かくして得られた焼結コアの、周波数: 100kHz
最大磁束密度:0.2T,温度:80゜Cにおける鉄損
値を交流Bl{ループトレーサーにて測定した結果を表
1に併記する。Frequency of the thus obtained sintered core: 100kHz
Table 1 also shows the results of measuring the iron loss value at maximum magnetic flux density: 0.2T and temperature: 80°C using an AC Bl {loop tracer.
第
■
表
表1から明らかなように、この発明に従い副成分として
sioZI CaO+ NbzOsならびに問3及び/
又はMo03を複合添加したものは、優れた低鉄損値が
得られている。Table 1 As is clear from Table 1, according to the present invention, sioZI CaO+ NbzOs and Question 3 and/or
Or, when Mo03 is added in combination, an excellent low core loss value is obtained.
これ対し、この発明の適正範囲を外れたもの(比較例)
はいずれも、鉄損の改善効果は少なく、甚だしい場合に
は異常粒或長によって鉄損特性は大幅に劣化している。On the other hand, those outside the appropriate range of this invention (comparative example)
In either case, the effect of improving iron loss is small, and in extreme cases, iron loss characteristics are significantly deteriorated due to abnormal grain length.
(発明の効果)
かくしてこの発明によれば、スイッチング周波数が10
0 kHz以上の高周波電源用トランスとして用いた場
合であっても損失が極めて小さいMn−Zn系ソフトフ
ェライトを得ることができる。(Effect of the invention) Thus, according to this invention, the switching frequency is 10
Even when used as a transformer for a high frequency power supply of 0 kHz or more, it is possible to obtain an Mn-Zn based soft ferrite with extremely low loss.
99
Claims (1)
3〜37mol%および ZnO:8〜13mol% を基本成分とし、この基本成分に SiO_2:0.008〜0.030wt%、CaO:
0.02〜0.15wt% と、 酸化ニオブ:0.01〜0.08wt%、 酸化タングステン及び/又は酸化モリブ デン:0.02〜0.20wt% とを添加配合してなる低損失Mn−Zn系フェライト。1. Fe_2O_3: 52-54 mol%, MnO: 3
The basic components are 3 to 37 mol% and ZnO: 8 to 13 mol%, and these basic components include SiO_2: 0.008 to 0.030 wt%, CaO:
Low loss Mn-Zn made by adding and blending 0.02 to 0.15 wt%, niobium oxide: 0.01 to 0.08 wt%, and tungsten oxide and/or molybdenum oxide: 0.02 to 0.20 wt%. type ferrite.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1301880A JP2721410B2 (en) | 1989-11-22 | 1989-11-22 | Low loss Mn-Zn ferrite |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1301880A JP2721410B2 (en) | 1989-11-22 | 1989-11-22 | Low loss Mn-Zn ferrite |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH03163803A true JPH03163803A (en) | 1991-07-15 |
JP2721410B2 JP2721410B2 (en) | 1998-03-04 |
Family
ID=17902254
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1301880A Expired - Fee Related JP2721410B2 (en) | 1989-11-22 | 1989-11-22 | Low loss Mn-Zn ferrite |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2721410B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011162366A (en) * | 2010-02-05 | 2011-08-25 | Jfe Chemical Corp | MnZnNi-BASED FERRITE |
-
1989
- 1989-11-22 JP JP1301880A patent/JP2721410B2/en not_active Expired - Fee Related
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2011162366A (en) * | 2010-02-05 | 2011-08-25 | Jfe Chemical Corp | MnZnNi-BASED FERRITE |
Also Published As
Publication number | Publication date |
---|---|
JP2721410B2 (en) | 1998-03-04 |
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