JP2691302B2 - Dielectric porcelain composition - Google Patents
Dielectric porcelain compositionInfo
- Publication number
- JP2691302B2 JP2691302B2 JP1204262A JP20426289A JP2691302B2 JP 2691302 B2 JP2691302 B2 JP 2691302B2 JP 1204262 A JP1204262 A JP 1204262A JP 20426289 A JP20426289 A JP 20426289A JP 2691302 B2 JP2691302 B2 JP 2691302B2
- Authority
- JP
- Japan
- Prior art keywords
- dielectric
- resonance frequency
- dielectric constant
- bao
- small
- 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 - Fee Related
Links
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Inorganic Insulating Materials (AREA)
Description
【発明の詳細な説明】 (産業上の利用分野) 本発明はマイクロ波領域での共振器や回路基板材料と
して適した新規な誘電体磁器組成物に関する。Description: TECHNICAL FIELD The present invention relates to a novel dielectric ceramic composition suitable as a resonator or circuit board material in a microwave region.
(従来技術) 近年、自動車電話、コードレステレホン、パーナル無
線機、衛星放送受信機の実用化に伴うマイクロ波回路の
IC化への発展、ガン発振器の利用範囲の拡大、ガリウム
ヒ素電界効果型トランジスタ使用の発振器への応用など
マイクロ波領域での誘電体磁器が広く使用されている。(Prior art) In recent years, microwave circuits have been developed with the practical use of car phones, cordless telephones, personal radios, and satellite broadcast receivers.
Dielectric ceramics in the microwave region are widely used, such as development to IC, expansion of the use range of gun oscillators, and application to oscillators using gallium arsenide field effect transistors.
このようなマイクロ波用誘電体磁器は主に共振器に用
いられるが、そこに要求される特性として(1)誘電体
中では波長が1/εr1/2に短縮されるので、小型化の要
求に対して比誘電率が大きい事、(2)高周波での誘電
損失が小さいこと、(3)共振周波数の温度に対する変
化が小さいこと、即ち、比誘電率の温度依存性が小さく
且つ安定であること、以上の3特性が主として挙げられ
る。Such microwave dielectric porcelains are mainly used for resonators, and the characteristics required therefor are: (1) In the dielectric, the wavelength is shortened to 1 / εr 1/2 , Large relative permittivity against requirements, (2) Small dielectric loss at high frequencies, (3) Small change in resonance frequency with temperature, that is, small relative temperature dependency of relative permittivity and stable. There are three main characteristics mentioned above.
従来、この種の誘電体磁器としては、例えば、BaO−T
iO2系材料、BaO−REO−TiO2(但し、REOは希土類元素酸
化物、以下同様)系材料及びMgTiO3−CaTiO3系材料など
が知られている。Conventionally, as this type of dielectric ceramic, for example, BaO-T
An iO 2 -based material, a BaO-REO-TiO 2 (where REO is a rare earth oxide, the same applies hereinafter) -based material, a MgTiO 3 -CaTiO 3 -based material, and the like are known.
(発明が解決しようとする問題点) しかし乍ら、BaO−TiO2系材料では比誘電率εrが38
〜40と高く、また誘電損失tanδは2.0×10-4と小さい
が、単一相では共振周波数の温度依存性τfがゼロのも
のが得難く、組成変化に対する比誘電率及び比誘電率の
温度依存性の変化も大きいため、高い比誘電率、低い誘
電損失を維持したまま共振周波数の温度係数τfを安定
に小さく制御することが困難である。(Problems to be Solved by the Invention) However, the relative dielectric constant εr of the BaO—TiO 2 based material is 38.
40 and high and although the dielectric loss tanδ is as small as 2.0 × 10 -4, a single-phase hard to obtain those temperature dependence τf of the resonance frequency is zero, the temperature of the dielectric constant and the dielectric constant for the composition change Since the dependence greatly changes, it is difficult to stably control the temperature coefficient τf of the resonance frequency to be small while maintaining a high relative dielectric constant and a low dielectric loss.
また、BaO−REO−TiO2系材料についてはBaO−Nd2O3−
TiO2系あるいはBaO−Sm2O3−TiO2系等が知られている
が、これらの系では誘電率εrが40〜60と非常に高く、
また共振周波数の温度係数τfがゼロのものも得られて
いるが誘電損失tanδは5.0×10-4以上と大きい。Also, the BaO-REO-TiO 2 based materials BaO-Nd 2 O 3 -
TiO 2 system or BaO-Sm 2 O 3 -TiO 2 system and the like are known, but in these systems, the dielectric constant εr is as high as 40 to 60,
Although the one having a zero temperature coefficient τf of the resonance frequency has been obtained, the dielectric loss tan δ is as large as 5.0 × 10 -4 or more.
さらにMgTiO3−CaTiO3系では誘電損失tanδは2.0×10
-4以下と小さく、共振周波数の温度係数τfがゼロのも
のも得られているが誘電率が16〜25と小さい。Furthermore, in the MgTiO 3 -CaTiO 3 system, the dielectric loss tanδ is 2.0 × 10
-4f or less, and a temperature coefficient τf of the resonance frequency of zero is obtained, but the dielectric constant is as small as 16 to 25.
このように、上記の何れの材料においても高周波用誘
電体材料に要求される前記3特性を共に充分には満足し
ていない。As described above, none of the above-mentioned materials sufficiently satisfies the three characteristics required for the high-frequency dielectric material.
(発明の目的) 本発明は上記の欠点に鑑み案出されたもので、共振器
の小型化を可能とするため、誘電率が高く(30以上)、
可能な限り誘電損失を低く誘電率の温度依存性が小さく
かつ安定で、誘電体共振器の共振周波数の温度依存性が
小さくかつ安定な高周波用誘電体磁器組成物を提供せん
とするものである。(Object of the Invention) The present invention has been devised in view of the above-mentioned drawbacks, and has a high dielectric constant (30 or more) in order to enable the miniaturization of a resonator.
It is an object of the present invention to provide a high-frequency dielectric ceramic composition having a low dielectric loss and a small and stable temperature dependence of a dielectric constant, and a small and stable temperature dependence of a resonance frequency of a dielectric resonator. .
(問題点を解決するための手段) 本発明者等は上記問題に対し、研究を重ねた結果、酸
化バリウム(BaO)、酸化サマリウム(Sm2O3)に対し、
酸化ニオブ(Nb2O5)或いは酸化タンタル(Ta2O5)を個
々に、あるいは組合せによって得られる組成式(1) Ba Sm1/2(NbxTa1-x)1/2O3 ・・・(1) 但し 0≦x≦1 で表される磁器組成物が高周波用として高い誘電率を有
し且つ低い誘電損失を維持するとともに、共振周波数の
温度依存性が小さく、且つ安定な特性を示すことを知見
し、本発明に至った。(Means for Solving Problems) As a result of repeated studies on the above problems, the present inventors have found that barium oxide (BaO) and samarium oxide (Sm 2 O 3 )
Composition formula (1) Ba Sm 1/2 (Nb x Ta 1-x ) 1/2 O 3 · obtained by individually or in combination with niobium oxide (Nb 2 O 5 ) or tantalum oxide (Ta 2 O 5 ). .. (1) However, the ceramic composition represented by 0 ≦ x ≦ 1 has a high dielectric constant for high frequencies and maintains a low dielectric loss, and the temperature dependence of the resonance frequency is small and stable characteristics. Therefore, the present invention has been completed.
本発明における上記式(1)の誘電磁器組成物は、A
サイトがBa、BサイトがSm1/2(NbxTa1-x)1/2で表され
るようにSm、Nb、Taの2種あるいは3種のイオンで構成
された複合ペロブスカイト型結晶構造の単一相であっ
て、各組成比が前記式(1)に示す各々の割合から外れ
るとペロブスカイト型結晶構造がくずれ、単一相でなく
なると同時に優れた誘電特性が劣化する。The dielectric ceramic composition of the above formula (1) in the present invention is
A complex perovskite crystal structure composed of two or three ions of Sm, Nb, and Ta, as represented by the site Ba and the site B Sm 1/2 (Nb x Ta 1-x ) 1/2 If the composition ratio is out of the respective ratios shown in the above formula (1), the perovskite type crystal structure collapses, the composition is not a single phase, and at the same time excellent dielectric properties are deteriorated.
本発明において磁器を製造する場合は、磁器を構成す
る金属の酸化物、即ちBaO、Sm2O3、Nb2O5並びにTa2O5あ
るいは焼成によて前記酸化物に変換し得る、例えば炭酸
塩、硝酸塩、硫酸塩等の化合物を用いて秤量混合後、所
望により1200〜1500℃で仮焼する。この混合物あるいは
仮焼粉末を成型後、1500〜1700℃の大気中で焼成するこ
とによって磁器を得ることができる。In the case of producing a porcelain in the present invention, an oxide of a metal constituting the porcelain, that is, BaO, Sm 2 O 3 , Nb 2 O 5 and Ta 2 O 5 or can be converted to the oxide by firing, for example, Compounds such as carbonates, nitrates and sulfates are weighed and mixed, and then calcined at 1200 to 1500 ° C. if desired. After molding this mixture or calcined powder, it is fired in the air at 1500 to 1700 ° C. to obtain a porcelain.
以下、本発明を次の例で説明する。 Hereinafter, the present invention will be described with reference to the following examples.
(実施例) 出発原料として高純度の炭酸バリウム(BaCO3)、酸
化サマリウム(Sm2O3)、酸化ニオブ(Nb2O5)、酸化タ
ンタル(Ta2O5)の各粉末を用いてそれらを前記式
(1)中のx値が第1表の割合になるように秤量後、純
水を加えめのう玉石を用いて一昼夜湿式混合を行なっ
た。この混合物を乾燥後、1400℃で2時間仮焼し、さら
に約1重量%のバインダーを加えてから整粒し、得られ
た粉末を約1000kg/cm2の圧力で成形し、それを1500〜17
00℃の温度で2時間空気中において焼成した。(Example) Using high-purity barium carbonate (BaCO 3 ), samarium oxide (Sm 2 O 3 ), niobium oxide (Nb 2 O 5 ), and tantalum oxide (Ta 2 O 5 ) powders as starting materials Was weighed so that the x value in the above formula (1) was in the ratio shown in Table 1, and then pure water was added and wet mixing was performed overnight using agate stones. After this mixture was dried, it was calcined at 1400 ° C for 2 hours, further added with about 1% by weight of a binder, and then sized, and the obtained powder was molded under a pressure of about 1000 kg / cm 2 , 17
Calcination was performed in air at a temperature of 00 ° C. for 2 hours.
得られた磁器を平面研磨及び円筒研削しφ約8mm、高
さ約4mmのゆがみのない円柱サンプルを得た。このサン
プルを用いて誘電体円柱共振器法により、共振周波数8
〜10GHzにて誘電率(εr)、誘電損失tanδ、共振周波
数の温度係数(τf)を測定し、τfは、−40〜+85℃
について測定した。結果は第1表に示す。The obtained porcelain was subjected to surface polishing and cylindrical grinding to obtain a distortion-free cylindrical sample having a diameter of about 8 mm and a height of about 4 mm. Using this sample, a resonance frequency of 8 was obtained by the dielectric cylinder resonator method.
Measure dielectric constant (εr), dielectric loss tanδ, temperature coefficient of resonance frequency (τf) at 1010 GHz, τf is −40 to + 85 ° C.
Was measured. The results are shown in Table 1.
第1表からも明らかなように、本発明の誘電体は、比
誘電率33以上、Q値4000以上、τfが25(ppm/℃)以下
の特性が得られ、またNbとTaの成分比を変更することに
よって、+1〜23(ppm/℃)の範囲でτfをコントロー
ルすることができる優れた特性が得られた。 As is clear from Table 1, the dielectric material of the present invention has characteristics of relative permittivity of 33 or more, Q value of 4000 or more, and τf of 25 (ppm / ° C) or less, and the composition ratio of Nb and Ta. By changing the value, excellent characteristics capable of controlling τf within the range of +1 to 23 (ppm / ° C) were obtained.
(発明の効果) 以上詳述した通り、本発明の誘電体磁器組成物はBa
O、Sm2O3、Nb2O5、Ta2O5からなる複合ペロブスカイト型
結晶構造を形成させることによって、高周波に対して高
い誘電率、低い誘電損失、及び共振周波数の温度係数の
小さい誘電特性が得られる。それと同時に共振器あるい
は回路基板材料としての用途に対し満足したものが得ら
れると同時に小型化も可能とすることができる。(Effect of the Invention) As described in detail above, the dielectric ceramic composition of the present invention is
By forming a composite perovskite type crystal structure consisting of O, Sm 2 O 3 , Nb 2 O 5 and Ta 2 O 5 , a high dielectric constant with respect to high frequencies, a low dielectric loss, and a dielectric with a low temperature coefficient of resonance frequency. The characteristics are obtained. At the same time, a material that is satisfactory for use as a resonator or circuit board material can be obtained, and at the same time, downsizing can be achieved.
Claims (1)
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1204262A JP2691302B2 (en) | 1989-08-07 | 1989-08-07 | Dielectric porcelain composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1204262A JP2691302B2 (en) | 1989-08-07 | 1989-08-07 | Dielectric porcelain composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH0369547A JPH0369547A (en) | 1991-03-25 |
JP2691302B2 true JP2691302B2 (en) | 1997-12-17 |
Family
ID=16487552
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1204262A Expired - Fee Related JP2691302B2 (en) | 1989-08-07 | 1989-08-07 | Dielectric porcelain composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP2691302B2 (en) |
-
1989
- 1989-08-07 JP JP1204262A patent/JP2691302B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
JPH0369547A (en) | 1991-03-25 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
LAPS | Cancellation because of no payment of annual fees |