JPH063683B2 - Dielectric porcelain composition - Google Patents
Dielectric porcelain compositionInfo
- Publication number
- JPH063683B2 JPH063683B2 JP61031991A JP3199186A JPH063683B2 JP H063683 B2 JPH063683 B2 JP H063683B2 JP 61031991 A JP61031991 A JP 61031991A JP 3199186 A JP3199186 A JP 3199186A JP H063683 B2 JPH063683 B2 JP H063683B2
- Authority
- JP
- Japan
- Prior art keywords
- dielectric
- present
- composition
- resonator
- antimony
- 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.)
- Expired - Lifetime
Links
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Ceramic Capacitors (AREA)
- Inorganic Insulating Materials (AREA)
Description
【発明の詳細な説明】 〔産業上の利用分野〕 本発明は誘電体共振器材料として好適なバリウム,亜
鉛,(ニオブ),アンチモンおよび酸素からなる誘電体
磁気組成物に関するものである。TECHNICAL FIELD The present invention relates to a dielectric magnetic composition containing barium, zinc, (niobium), antimony and oxygen, which is suitable as a dielectric resonator material.
更に詳しくは,本発明はマイクロ波周波数帯で使用され
る誘電体共振器としたときに無負荷Q(Qu)が大きく、用
途に応じて比誘電率(εr)および共振周波数の温度計数
(τf)を広い範囲で任意に制御可能な誘電体磁器組成物
に関するものである。More specifically, the present invention has a large unloaded Q (Qu) when used as a dielectric resonator used in the microwave frequency band, and the relative permittivity (ε r ) and the temperature coefficient of the resonance frequency are determined according to the application.
The present invention relates to a dielectric ceramic composition in which (τ f ) can be arbitrarily controlled in a wide range.
誘電体共振器の大きさは一般に に反比例し,比誘電率が大きいほど,共振器を小さくで
き回路を小型化できるので共振器材料の磁器組成物とし
ては、無負荷Qが大きく,共振周波数の温度係数の安定
度がすぐれていると共に,一般に,比電率の大きなもの
が望ましいが,比誘電率が極端に大きすぎるとあまりに
も共振器が小さくなりずきかえって取扱いが困難になる
ため、共振器が使用される周波数帯によって要求される
比誘電率の値も異なってくる。The size of the dielectric resonator is generally Inversely proportional to, the larger the relative permittivity, the smaller the resonator and the circuit can be made. Therefore, as a ceramic composition of the resonator material, the unloaded Q is large and the stability of the temperature coefficient of the resonance frequency is excellent. At the same time, it is generally desirable to have a large relative electric permittivity, but if the relative permittivity is too large, the resonator will not be too small and will be difficult to handle. Therefore, it may be required depending on the frequency band in which the resonator is used. The value of the relative permittivity also varies.
従来誘電体共振器材料として共振器に使用される磁気組
成物としては、Ba(Mg1/3Ta2/3)O3系(特公昭59−23
048号公報),Ba(Zn1/3Ta2/3)O3系(特公昭59−4
8484号公報),Ba(Zn1/3Nb2/3)O3系(特開昭53−
35453号公報),Ba(Mg1/3Nd2/3)O3系(特開昭53
−35345号公報),CaTiO3-MgTiO3-La2O3・2tiO
2系,Sr(Zn1/3Nd2/3)O3−SrTiO3系等すでに多数提案さ
れている。A magnetic composition conventionally used for a resonator as a dielectric resonator material is Ba (Mg 1/3 Ta 2/3 ) O 3 system (Japanese Patent Publication No. 59-23).
048), Ba (Zn 1/3 Ta 2/3 ) O 3 system (Japanese Patent Publication No. 59-4).
8484), Ba (Zn 1/3 Nb 2/3 ) O 3 system (JP-A-53-
35453), Ba (Mg 1/3 Nd 2/3 ) O 3 system (JP-A-5353)
-35345 discloses), CaTiO 3 -MgTiO 3 -La 2 O 3 · 2tiO
Many have already been proposed such as the 2 system, the Sr (Zn 1/3 Nd 2/3 ) O 3 —SrTiO 3 system.
しかしながら,従来公知の磁器組成物,例えばBa(Zn1/3
Nd2/3)O3およびBa(Zn1/3Ta2/3)O3等の単独磁器組成物は
これらの組成物固有の比誘電率および共振周波数の温度
係数を有し,任意に制御することができないことから,
マイクロ波周波数帯で使用される共振器材料としては実
用上不都合な点が多い。However, conventionally known porcelain compositions such as Ba (Zn 1/3
Single porcelain compositions such as Nd 2/3 ) O 3 and Ba (Zn 1/3 Ta 2/3 ) O 3 have their own specific dielectric constant and temperature coefficient of resonance frequency, and can be controlled arbitrarily. Because I cannot do it,
As a resonator material used in the microwave frequency band, there are many practical disadvantages.
発明の目的は無負荷Qが大きく,しかも比誘電率および
共振周波数の温度係数を広い範囲で任意に制御可能な誘
電体磁器組成物を提供することにある。An object of the present invention is to provide a dielectric ceramic composition having a large unloaded Q and capable of arbitrarily controlling the relative permittivity and the temperature coefficient of the resonance frequency in a wide range.
本発明の目的は,単独組成では比誘電率および共振周波
数の温度係数を任意に制御することができないBa(Zn1/3
Nb2/3)O3系のNbの一部または全部をアンチモンで置換し
た磁気組成物によって達成される。The object of the present invention is to prevent the Ba (Zn 1/3
This is achieved by a magnetic composition in which a part or all of Nb 2/3 ) O 3 Nb is replaced with antimony.
本発明はバリウム,亜鉛,ニオブ,アンチモンおよび酸
素からなる式, Ba〔Zn1/3(Nb1-XSbx)2/3〕O3 (式中 0<x≦1,好ましくは0.001<x≦1) で表わされる誘電体磁器組成物に関するものである。The present invention includes a formula consisting of barium, zinc, niobium, antimony and oxygen, Ba [Zn 1/3 (Nb 1-X Sbx) 2/3 ] O 3 (wherein 0 <x ≦ 1, preferably 0.001 <x ≦ The present invention relates to a dielectric ceramic composition represented by 1).
本発明の組成物においてアンチモンは比誘電率および共
振周波数の温度係数を任意に制御する働きとともにQ値
の改善に大きく作用している。In the composition of the present invention, antimony has a function of arbitrarily controlling the relative dielectric constant and the temperature coefficient of the resonance frequency and also has a great effect on the improvement of the Q value.
なお,アンチモンを含有しない組成物,すなわちBa(Zn
1/3(Zn1/3Nb2/3)O3は共振周波数の温度係数が大きすぎ
るという難点がある。The composition containing no antimony, namely Ba (Zn
1/3 (Zn 1/3 Nb 2/3 ) O 3 has a drawback that the temperature coefficient of the resonance frequency is too large.
本発明による誘電体磁器組成物は,バリウム,亜鉛,ニ
オブ,アンチモン等の炭素塩,酸化物等の出発原料を混
合して仮焼した後,成形,焼成して焼結させる方法で製
造することができる。The dielectric porcelain composition according to the present invention is manufactured by a method in which starting materials such as carbon salts and oxides of barium, zinc, niobium, antimony, etc. are mixed and calcined, followed by molding and firing to sinter. You can
例えば,炭酸バリウム,酸化亜鉛,五酸化ニオブおよび
三酸化アンチモンの各所定量を水,アルコール等を除去
した後,粉砕し、酸素含有ガス雰囲気(例えば空気雰囲
気)下に800〜1400℃で約10時間程度仮焼す
る。これによって形成された仮焼物を粉砕した後,ポリ
ビニルアルコールの如き有機バインダと共に混合して均
質にし,乾燥,粉砕して加圧成形(圧力100〜300
0Kg/cm2)する。そして,この成形物を空気の如き酸
素含有ガス雰囲気下に1300〜1600℃で焼成すれ
ば,本発明の誘電体磁器組成物が得られる。For example, barium carbonate, zinc oxide, niobium pentoxide, and antimony trioxide are removed from water, alcohol, and the like in predetermined amounts, and then pulverized, and the mixture is crushed in an oxygen-containing gas atmosphere (eg, air atmosphere) at 800 to 1400 ° C. for about 10 hours. Calcination about. The calcined material formed by this is crushed, then mixed with an organic binder such as polyvinyl alcohol to be homogenized, dried, crushed and pressure-molded (pressure 100 to 300).
0 kg / cm 2 ). Then, the dielectric ceramic composition of the present invention can be obtained by firing this molded product at 1300 to 1600 ° C. in an oxygen-containing gas atmosphere such as air.
こうして得られた誘電体磁器組成物は,これをそのまま
又は必要に応じて適当な形状およびサイズに加工すると
誘電体共振器になる。また本発明の誘電体磁器組成物
は、マイクロ波IC用誘電体基板,誘電体調整棒等の材
料として利用することができる。The dielectric ceramic composition thus obtained becomes a dielectric resonator when it is processed as it is or into an appropriate shape and size as required. Further, the dielectric ceramic composition of the present invention can be used as a material for a dielectric substrate for microwave IC, a dielectric adjusting rod, and the like.
実施例1 炭酸バリウム(BaCO3)粉末0.6モル,酸化亜鉛(ZnO)
粉末0.2モル,酸化ニオブ(Nb2O5)粉末0.198モルおよ
び三酸化アンチモン(Sb2O3)粉末0.02モルをエタノー
ルと共にボールミルに入れ,16時間湿式混合した。こ
の混合物をボールミルから取り出して溶媒のエタノール
を蒸発させ,らい潰機で2時間粉砕した。粉砕物は,空
気雰囲気下に1300℃仮焼した後,再びらい潰機で1
時間粉砕した。この粉砕物は適量のポリビニルアルコー
ル溶液を加えて均一に混合した後,直径15mmφ,厚さ
7mmの円盤状ペレットに成形して空気雰囲気下に153
0℃で4時間焼成,焼結して本発明の誘電体磁器組成物
を得た。Example 1 Barium carbonate (BaCO 3 ) powder 0.6 mol, zinc oxide (ZnO)
0.2 mol of powder, 0.198 mol of niobium oxide (Nb 2 O 5 ) powder and 0.02 mol of antimony trioxide (Sb 2 O 3 ) powder were put in a ball mill together with ethanol and wet-mixed for 16 hours. The mixture was taken out of the ball mill, the solvent ethanol was evaporated, and the mixture was pulverized with a muller for 2 hours. The crushed product is calcined in an air atmosphere at 1300 ° C and then re-crushed with a crusher.
Crushed for hours. This pulverized product was mixed with an appropriate amount of polyvinyl alcohol solution and uniformly mixed, and then molded into a disk-shaped pellet having a diameter of 15 mmφ and a thickness of 7 mm, which was then subjected to 153 in an air atmosphere.
The dielectric ceramic composition of the present invention was obtained by firing and sintering at 0 ° C. for 4 hours.
こうして得られた磁器組成物を直径11mmφ,厚さ4.3m
mの大きさにカットした後、誘電共振法によって測定
し、共振周波数fo(4.5〜5.5GHz)における無負荷Qお
よび比誘電率εrを求めた。また、共振周波数の温度依
存性については−40〜50℃の範囲で測定した温度係
数τfを求めた。その結果を第1表に示す。The porcelain composition thus obtained had a diameter of 11 mm and a thickness of 4.3 m.
After cutting to a size of m, measurement was performed by the dielectric resonance method, and the unloaded Q and the relative permittivity ε r at the resonance frequency f o (4.5 to 5.5 GHz) were obtained. Regarding the temperature dependence of the resonance frequency, the temperature coefficient τ f measured in the range of −40 to 50 ° C. was obtained. The results are shown in Table 1.
実施例2〜5 実施例1の五酸化ニオブおよび三酸化アンチモンの使用
量を変え式Ba〔Zn1/3(Nb1-XSbx)2/3〕O3におけるその値
が第1表記載の誘電体磁器組成物を製造し実施例1と同
様にして電気的特性を測定した。Examples 2 to 5 The values in the formula Ba [Zn 1/3 (Nb 1-X Sbx) 2/3 ] O 3 were changed from those in Table 1 by changing the amounts of niobium pentoxide and antimony trioxide used in Example 1. A dielectric porcelain composition was produced and its electrical characteristics were measured in the same manner as in Example 1.
ただし,実施例5に記載の磁器組成物のみ直径7mmφ,
厚さ4.3mmの円盤状にカットした後,共振周波数(fo)
10〜11GHzにおける電気的特性を測定した。However, only the porcelain composition described in Example 5 had a diameter of 7 mmφ,
Resonance frequency (f o ) after cutting into a disc with a thickness of 4.3 mm
The electrical characteristics at 10 to 11 GHz were measured.
それらの結果を第1表に示す。The results are shown in Table 1.
比較例1 実施例1の酸化アンチモンを使用せずに焼成温度を15
30℃としたほかは実施例1と同様にして誘電体磁器組
成物〔(Ba(Zn1/3(Nb1/3Nb2/3)O3〕を製造し,実施例1
と同様にして電気的特性を測定した。Comparative Example 1 The firing temperature was adjusted to 15 without using the antimony oxide of Example 1.
A dielectric ceramic composition [(Ba (Zn 1/3 (Nb 1/3 Nb 2/3 ) O 3 ]) was produced in the same manner as in Example 1 except that the temperature was 30 ° C.
The electrical characteristics were measured in the same manner as in.
その結果,Q=1000,εr=38.8,τf=36ppm
/℃であった。As a result, Q = 1000, ε r = 38.8, τ f = 36 ppm
/ ° C.
〔発明の効果〕 本発明の誘電体磁器組成物は,無負荷Qが大きいだけで
なく,比誘電率および共振周波数の温度係数を任意に制
御できるので,各周波数帯の誘電体共振器材料として好
適である。 [Advantages of the Invention] The dielectric ceramic composition of the present invention has not only a large unloaded Q, but also can control the relative permittivity and the temperature coefficient of the resonance frequency as desired, so that it can be used as a dielectric resonator material for each frequency band. It is suitable.
また,本発明の誘電体磁器組成物を用い,例えばマイク
ロ波周波数帯用共振器として使用すると,受信機の性能
を大幅に向上させることができるという利点がある。Further, when the dielectric ceramic composition of the present invention is used, for example, as a resonator for microwave frequency band, there is an advantage that the performance of the receiver can be greatly improved.
Claims (1)
び酸素からなる式 Ba〔Zn1/3(Nb1-XSbx)2/3〕O3 (式中 0<x≦1) で表わされる誘電体磁器組成物。1. A dielectric material represented by the formula Ba [Zn 1/3 (Nb 1-X Sbx) 2/3 ] O 3 (where 0 <x ≦ 1) consisting of barium, zinc, niobium, antimony and oxygen. Porcelain composition.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61031991A JPH063683B2 (en) | 1986-02-18 | 1986-02-18 | Dielectric porcelain composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP61031991A JPH063683B2 (en) | 1986-02-18 | 1986-02-18 | Dielectric porcelain composition |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS62190608A JPS62190608A (en) | 1987-08-20 |
| JPH063683B2 true JPH063683B2 (en) | 1994-01-12 |
Family
ID=12346386
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP61031991A Expired - Lifetime JPH063683B2 (en) | 1986-02-18 | 1986-02-18 | Dielectric porcelain composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH063683B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP4524411B2 (en) * | 2001-06-20 | 2010-08-18 | 日本特殊陶業株式会社 | Dielectric porcelain composition |
Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5948483B2 (en) | 2012-03-23 | 2016-07-06 | フロニウス・インテルナツィオナール・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングFronius International Gmbh | Welding device with touch screen |
-
1986
- 1986-02-18 JP JP61031991A patent/JPH063683B2/en not_active Expired - Lifetime
Patent Citations (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5948483B2 (en) | 2012-03-23 | 2016-07-06 | フロニウス・インテルナツィオナール・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングFronius International Gmbh | Welding device with touch screen |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS62190608A (en) | 1987-08-20 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH063683B2 (en) | Dielectric porcelain composition | |
| JP2974170B2 (en) | Dielectric porcelain composition | |
| JP3243874B2 (en) | Dielectric porcelain composition | |
| JPH0712971B2 (en) | Dielectric porcelain composition | |
| JPH06309926A (en) | Dielectric ceramic composition | |
| JPH06325620A (en) | Dielectric porcelain composition | |
| JPH0642327B2 (en) | Dielectric porcelain composition | |
| JP3291780B2 (en) | Dielectric porcelain composition | |
| JP3257147B2 (en) | Dielectric porcelain composition | |
| JP2974171B2 (en) | Dielectric porcelain composition | |
| JP3243873B2 (en) | Dielectric porcelain composition | |
| JP3243890B2 (en) | Dielectric porcelain composition | |
| JPH06333421A (en) | Dielectric porcelain composition | |
| JPH0642326B2 (en) | Dielectric porcelain composition | |
| JPH06139820A (en) | Dielectric porcelain composition | |
| JP2974172B2 (en) | Dielectric porcelain composition | |
| JPH06333422A (en) | Dielectric ceramic composition | |
| JP2002255640A (en) | Dielectric ceramic composition | |
| JPH06325621A (en) | Dielectric ceramic composition | |
| JPH0616364B2 (en) | Dielectric porcelain composition | |
| JPH06349327A (en) | Dielectric porcelain composition | |
| JPH02275756A (en) | dielectric porcelain composition | |
| JPH06349331A (en) | Dielectric porcelain composition | |
| JPH06349335A (en) | Dielectric porcelain composition | |
| JPH06333425A (en) | Dielectric porcelain composition |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EXPY | Cancellation because of completion of term |