JPH0644407B2 - Dielectric porcelain - Google Patents

Dielectric porcelain

Info

Publication number
JPH0644407B2
JPH0644407B2 JP61178824A JP17882486A JPH0644407B2 JP H0644407 B2 JPH0644407 B2 JP H0644407B2 JP 61178824 A JP61178824 A JP 61178824A JP 17882486 A JP17882486 A JP 17882486A JP H0644407 B2 JPH0644407 B2 JP H0644407B2
Authority
JP
Japan
Prior art keywords
dielectric
porcelain
dielectric porcelain
present
resonance frequency
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
Application number
JP61178824A
Other languages
Japanese (ja)
Other versions
JPS6337508A (en
Inventor
和順 松本
健裕 日向
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.)
Sumitomo Metal Mining Co Ltd
Original Assignee
Sumitomo Metal Mining 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 Sumitomo Metal Mining Co Ltd filed Critical Sumitomo Metal Mining Co Ltd
Priority to JP61178824A priority Critical patent/JPH0644407B2/en
Priority to CA000540834A priority patent/CA1296177C/en
Priority to DE8787305786T priority patent/DE3776437D1/en
Priority to EP19870305786 priority patent/EP0252668B1/en
Publication of JPS6337508A publication Critical patent/JPS6337508A/en
Priority to US07/240,448 priority patent/US4830995A/en
Publication of JPH0644407B2 publication Critical patent/JPH0644407B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明は誘電体磁器に関し、特に、高周波領域におい
て、高い無負荷Qを有する高周波用として好適である誘
電体磁器に関する。
Description: TECHNICAL FIELD The present invention relates to a dielectric ceramic, and more particularly to a dielectric ceramic suitable for high frequencies having a high unloaded Q in a high frequency region.

〔従来の技術〕[Conventional technology]

一般に、マイクロ波やミリ波などの高周波領域の信号回
路に使用される誘電体共振器や誘電体基板には、高い誘
電率および高い無負荷Qを有し、しかも共振周波数の温
度係数の絶対値が小さい誘電体磁器を用いることが望ま
れている。従来、この種の誘電体磁器として、TiO2系の
材料がよく利用され、例えば、BaO-TiO2系、ZrO2-SnO2-
TiO2系の材料、最近では、Ba(Zn,TA)O3系、Ba(Mg,Ta)O3
系の材料等がある。これらの材料からなる誘電体磁器
は、10GHz程度の高周波数において無負荷Qが3000〜
7000、誘電率が20〜40、共振周波数の温度係数が0
ppm/℃近傍という特性を有している。
Generally, a dielectric resonator or a dielectric substrate used for a signal circuit in a high frequency region such as a microwave or a millimeter wave has a high dielectric constant and a high unloaded Q, and the absolute value of the temperature coefficient of the resonance frequency. It is desired to use a dielectric porcelain having a small value. Conventionally, TiO 2 -based materials are often used as this type of dielectric porcelain, for example, BaO-TiO 2 -based, ZrO 2 -SnO 2-
TiO 2 based materials, recently Ba (Zn, TA) O 3 based, Ba (Mg, Ta) O 3
There are materials for the system. Dielectric porcelain made of these materials has a no-load Q of 3000 ~ at high frequencies of about 10 GHz.
7,000, dielectric constant 20-40, temperature coefficient of resonance frequency is 0
It has a characteristic of around ppm / ° C.

〔発明が解決しようとする問題点〕[Problems to be solved by the invention]

ところで、近年、通信機器に使用される周波数の高周波
化が進み、衛星放送等に使われるSHF帯においてもこ
れまでより一層高い無負荷Qを有する誘電体磁器が求め
られている。
By the way, in recent years, the frequencies used in communication devices have become higher, and there is a demand for dielectric porcelain having even higher unloaded Q even in the SHF band used for satellite broadcasting and the like.

そこで、本発明の目的は、一層高い無負荷Qを示す新規
な系の誘電体磁器を提供することにある。
Therefore, an object of the present invention is to provide a new type of dielectric porcelain exhibiting a higher unloaded Q.

〔問題点を解決するための手段〕[Means for solving problems]

すなわち、本発明は、前記問題点を解決するものとし
て、 一般式(I): (Ba1-xSrx)(Mg1-yNiy)1-u(Ta1-zNbz)uO2+(3/2)u 〔式中、x,y,zおよびuは、それぞれ、0<x≦
0.25、0<y≦0.5、0≦z≦0.8、0.61≦u≦
0.72で表わされる数である。〕 で表わされる組成を有する誘電体磁器を提供するもので
ある。
That is, the present invention provides a solution to the above-mentioned problems by the general formula (I): (Ba 1-x Sr x ) (Mg 1-y Ni y ) 1-u (Ta 1-z Nb z ) u O 2+ (3/2) u [wherein x, y, z and u are respectively 0 <x ≦
0.25, 0 <y ≦ 0.5, 0 ≦ z ≦ 0.8, 0.61 ≦ u ≦
It is a number represented by 0.72. ] The present invention provides a dielectric ceramic having a composition represented by:

本発明の誘電体磁器は、かかる成分組成により、高い誘
電率と温度煩存性の少ない共振周波数を有する上に、高
周波領域において著しく増大した無負荷Qを有する磁器
が得られることを見出したものである。
It has been found that the dielectric porcelain of the present invention can obtain a porcelain having not only a high dielectric constant and a resonance frequency with little temperature complication but also a significantly increased unloaded Q in a high frequency region due to such a composition. Is.

すなわち、一般式(I)において、x,y,zおよびu
の範囲はそれぞれ0<x≦0.25、0<y≦0.5、
0≦z≦0.8、0.61≦u≦0.72である。xは
0、即ちSrが含有されないと焼結が困難となり、0.2
5を超えると共振周波数の温度係数が正の方向に急増し
てしまう。yは0.5を超えると無負荷Qが低下する。
また、zは0でも、即ちNbが含有されなくてもよいが、
0.8を超えると無負荷Qが低下すると共に、共振周波
数の温度係数が正に大きくなり過ぎる。
That is, in the general formula (I), x, y, z and u
Ranges of 0 <x ≦ 0.25, 0 <y ≦ 0.5,
0 ≦ z ≦ 0.8 and 0.61 ≦ u ≦ 0.72. x is 0, that is, if Sr is not contained, sintering becomes difficult and 0.2
When it exceeds 5, the temperature coefficient of the resonance frequency increases rapidly in the positive direction. When y exceeds 0.5, the no-load Q decreases.
Further, z may be 0, that is, Nb may not be contained,
When it exceeds 0.8, the no-load Q decreases and the temperature coefficient of the resonance frequency becomes too positive.

本発明の誘電体磁器の製法については、特に制限はな
く、通常の方法により製造することができる。例えばB
a,Mg,Ni,TaおよびNb成分の原料として、それぞれ、
炭酸バリウム、炭酸ストロンチウム、酸化マグネシウ
ム、酸化ニッケル、酸化タンタルおよび酸化ニオブの粉
末をそれぞれ所望組成の磁器が得られるような割合で秤
量し、それらを十分に混合する。その混合物を仮焼に供
した後、粉砕し、加圧成形する。得られた成形体を1500
〜1650℃程度で焼成することにより本発明の誘電体磁器
を製造することができる。
The method for producing the dielectric ceramics of the present invention is not particularly limited and can be produced by a usual method. For example B
As raw materials for a, Mg, Ni, Ta and Nb components,
Powders of barium carbonate, strontium carbonate, magnesium oxide, nickel oxide, tantalum oxide and niobium oxide are weighed in proportions so as to obtain a porcelain having a desired composition, and they are mixed sufficiently. The mixture is calcined, then crushed and pressure-molded. The obtained molded body is 1500
The dielectric ceramic of the present invention can be manufactured by firing at about 1650 ° C.

〔実施例〕〔Example〕

以下、本発明を実施例および比較例により詳細に説明す
る。
Hereinafter, the present invention will be described in detail with reference to Examples and Comparative Examples.

原料として、それぞれ純度99.9モル%の炭酸バリウ
ム、炭酸ストロンチウム、酸化マグネシウム、酸化ニッ
ケル、酸化タンタルおよび酸化ニオブの粉末を用意し、
これら原料粉末を一般式(I)におけるx,y,zおよ
びuの値が第1表に示す21種の試料(*印を付した試
料は比較例、他は実施例)のそれとなるように各試料番
号ごとにそれぞれ秤量し、純水と共にボールミルのポッ
トに入れ、16時間湿式混合した。この混合物をポット
から取り出し、150℃で5時間乾燥した後、空気中に
おいて1000℃で2時間仮焼した。仮焼後、粉砕し、42
メッシュの篩を通して整粒した。得られた粉末を金型を
用いて圧力500kg/cm2で直径10mm、厚さ約5mmの
円板状に一次成形した後、圧力2000kg/cm2でラバープ
レスにて圧縮し、成形体とした。この成形体を酸素気流
中、1650℃で4時間焼成して磁器を得た。
Powders of barium carbonate, strontium carbonate, magnesium oxide, nickel oxide, tantalum oxide, and niobium oxide each having a purity of 99.9 mol% were prepared as raw materials,
The values of x, y, z and u in the general formula (I) of these raw material powders should be the same as those of 21 kinds of samples shown in Table 1 (samples marked with * are comparative examples, others are examples). Each sample number was weighed, put into a pot of a ball mill together with pure water, and wet mixed for 16 hours. The mixture was taken out of the pot, dried at 150 ° C. for 5 hours, and then calcined in air at 1000 ° C. for 2 hours. After calcination, crush, 42
The particles were sieved through a mesh sieve. The obtained powder was primary molded into a disk shape having a diameter of 10 mm and a thickness of about 5 mm at a pressure of 500 kg / cm 2 using a mold, and then compressed by a rubber press at a pressure of 2000 kg / cm 2 to obtain a molded body. . This molded body was fired in an oxygen stream at 1650 ° C. for 4 hours to obtain a porcelain.

得られた磁器の誘電率(εr)および無負荷Q(Qu)を
誘電体円柱共振器法により約10GHzの周波数において
測定した。また、−10℃から80℃の温度範囲における
共振周波数を測定し、20℃における共振周波数の温度
係数(τf)を算出した。得られた結果を第1表に示
す。
The dielectric constant (εr) and unloaded Q (Qu) of the obtained porcelain were measured at a frequency of about 10 GHz by the dielectric cylinder resonator method. Further, the resonance frequency in the temperature range of −10 ° C. to 80 ° C. was measured, and the temperature coefficient (τf) of the resonance frequency at 20 ° C. was calculated. The results obtained are shown in Table 1.

第1表より、本発明の実施例である試料番号1〜9の誘
電体磁器は、7,000以上の大きい無負荷Qを有している
ことがわかる。
It can be seen from Table 1 that the dielectric porcelains of sample numbers 1 to 9 which are examples of the present invention have a large unloaded Q of 7,000 or more.

〔発明の効果〕〔The invention's effect〕

本発明の誘電体磁器は、10GHz付近の高周波領域にお
いても無負荷Qが7,000以上という非常に高い値を有し
ており、最近の使用周波数の高周波化の要請に応え得る
ものである。
The dielectric porcelain of the present invention has a very high value of 7,000 or more with no load even in a high frequency region near 10 GHz, and can meet the recent demand for higher frequency usage.

しかも、共振周波数の温度係数の絶対値も小さく、誘電
率においても高い値を有しており、高周波用の誘電体共
振器や誘電体基板等に使用される誘電体磁器として極め
て有用なものである。
In addition, the absolute value of the temperature coefficient of the resonance frequency is small, and it has a high value of the dielectric constant, which makes it extremely useful as a dielectric ceramic used in high-frequency dielectric resonators and dielectric substrates. is there.

Claims (2)

【特許請求の範囲】[Claims] 【請求項1】一般式: (Ba1-xSrx)(Mg1-yNiy)1-uTauO2+(3/2)u 〔式中、x,yおよびuは、それぞれ、0<x≦0.2
5、0<y≦0.5、0.61≦u≦0.72で表わさ
れる数である。〕 で表わされる組成を有する誘電体磁器。
1. A general formula: (Ba 1-x Sr x ) (Mg 1-y Ni y ) 1-u Ta u O 2+ (3/2) u [wherein, x, y and u are respectively , 0 <x ≦ 0.2
5, 0 <y ≦ 0.5, 0.61 ≦ u ≦ 0.72. ] A dielectric porcelain having a composition represented by:
【請求項2】一般式: (Ba1-xSrx)(Mg1-yNiy)1-u(Ta1-zNbz)uO2+(3/2)u 〔式中、x,y,zおよびuは、それぞれ、0<x≦
0.25、0<y≦0.5、0<z≦0.8、0.61
≦u≦0.72で表わされる数である。〕 で表わされる組成を有する誘電体磁器。
2. A general formula: (Ba 1-x Sr x ) (Mg 1-y Ni y ) 1-u (Ta 1-z Nb z ) u O 2+ (3/2) u [wherein x , Y, z and u are respectively 0 <x ≦
0.25, 0 <y ≦ 0.5, 0 <z ≦ 0.8, 0.61
It is a number represented by ≦ u ≦ 0.72. ] A dielectric porcelain having a composition represented by:
JP61178824A 1986-02-21 1986-07-31 Dielectric porcelain Expired - Lifetime JPH0644407B2 (en)

Priority Applications (5)

Application Number Priority Date Filing Date Title
JP61178824A JPH0644407B2 (en) 1986-07-31 1986-07-31 Dielectric porcelain
CA000540834A CA1296177C (en) 1986-07-09 1987-06-29 Dielectric ceramics
DE8787305786T DE3776437D1 (en) 1986-07-09 1987-06-30 DIELECTRIC CERAMICS.
EP19870305786 EP0252668B1 (en) 1986-02-21 1987-06-30 Dielectric ceramics
US07/240,448 US4830995A (en) 1986-07-09 1988-09-02 Dielectric ceramics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61178824A JPH0644407B2 (en) 1986-07-31 1986-07-31 Dielectric porcelain

Publications (2)

Publication Number Publication Date
JPS6337508A JPS6337508A (en) 1988-02-18
JPH0644407B2 true JPH0644407B2 (en) 1994-06-08

Family

ID=16055304

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61178824A Expired - Lifetime JPH0644407B2 (en) 1986-02-21 1986-07-31 Dielectric porcelain

Country Status (1)

Country Link
JP (1) JPH0644407B2 (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2010558C (en) * 1989-02-23 1994-04-05 Masaaki Sugiyama Dielectric ceramic material and method of producing same
JP4790885B2 (en) * 1999-12-09 2011-10-12 日本特殊陶業株式会社 Dielectric resonator and method for manufacturing dielectric material for dielectric resonator

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6291417A (en) * 1985-10-15 1987-04-25 Ube Ind Ltd Production of raw material for easy-to-sinter perovskite and its solid solution by multiple wet method

Also Published As

Publication number Publication date
JPS6337508A (en) 1988-02-18

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