JPH0515006B2 - - Google Patents

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Publication number
JPH0515006B2
JPH0515006B2 JP60093426A JP9342685A JPH0515006B2 JP H0515006 B2 JPH0515006 B2 JP H0515006B2 JP 60093426 A JP60093426 A JP 60093426A JP 9342685 A JP9342685 A JP 9342685A JP H0515006 B2 JPH0515006 B2 JP H0515006B2
Authority
JP
Japan
Prior art keywords
dielectric
dielectric ceramic
sample
weight
equivalent
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
JP60093426A
Other languages
Japanese (ja)
Other versions
JPS61253710A (en
Inventor
Kazuo Sasazawa
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 JP60093426A priority Critical patent/JPS61253710A/en
Publication of JPS61253710A publication Critical patent/JPS61253710A/en
Publication of JPH0515006B2 publication Critical patent/JPH0515006B2/ja
Granted legal-status Critical Current

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Description

【発明の詳細な説明】[Detailed description of the invention]

〔産業上の利用分野〕 この発明は、共振周波数が10数GHzの誘電体共
振器用の誘電体磁器組成物に関する。 〔従来の技術〕 共振周波数が10数GHzの誘電体共振器の無負荷
のQの優れたものは、約10000である。この従来
の誘電体共振器の誘電体には、Ba・〔Zn1/3
Ta2/3・〔Zn1/3Nb2/31/3・O3の組成式で表される
誘電体磁器組成物が使用されていた。 〔発明が解決しようとする問題点〕 前述した従来の誘電体磁器組成物は、高価であ
つた。この理由は製造過程における焼成温度が約
1600℃と高いため、焼成炉の設備コストやその補
修コスト及び熱エネルギーのコスト等がかさみ、
これらによつて製造原価が高くなるからである。
従つて、より低い温度で焼成することができる誘
電体磁器組成物が要望されている。 この発明は、上記要望に基づいて創案されたも
ので、従来のものに比べて安価な誘電体磁器組成
物を提供するものである。 〔問題を解決するための手段〕 上記目的を達成するこの発明の誘電体磁器組成
物は、Ba・〔Mg(x)Co(1-x1/3・〔Ta(x)Nb(1-x)2/
・O3で表される組成式のxが0.3〜0.9の範囲で
ある複合ペロブスカイトを主成分とし、この100
重量部に対し、Al2O3、Cr2O3、Y2O3、Mn2O3
グループの一種以上の成分を0.01〜0.5重量部含
ませたものである。 〔実施例〕 次ぎに上記組成式におけるxの値が0.5である
Ba・(Mg0.5Co0.51/3・(Ta0.5Nb0.52/3・O3成分が
100重量部と、Cr2O3が0.1重量部からなる誘電体
磁器組成物の製造方法を説明する。 まず、BaCO3の粉末98.67g(0.500モル相当)、
MgOの粉末3.36g(0.083モル相当)、CoOの粉末
6.22g(0.083モル相当)、Ta2O5の粉末36.18g
(0.083モル相当)、Nb2O5の粉末22.06g(0.083モ
ル相当)及びCr2O3の粉末0.167g(上記BaCO3
からNb2O5までの成分の総量100重量部に対して
0.1重量部相当)をそれぞれ秤量した。この秤量
粉末を純水と共にボールミルに入れ、24時間湿式
混合した。 こうして得られた混合物を脱水して、150℃の
温度で5時間乾燥した後、1100℃の温度にて2時
間の仮焼を行つた。次ぎに仮焼物をボールミルで
粉砕した。この粉砕物にポリビニルアルコールを
3.0g加えて擂潰器で混合し、60メツシユのふる
いにかけて造粒した。これらの造粒物のうち0.66
gを金型に入れ、3ton/cm2の圧力をかけた。この
加圧成型を繰り返すことによつて、直径7.0mmφ、
厚さ3.5mmの円板を20個製作した。続いてこれら
の円板を1370℃の温度で4時間焼成し、直径約
6.0mm、厚さ約3.1mmの誘電体磁器円板を得た。 これら誘電体磁器円板の両面をラツプ研磨し、
厚さtを3.00mmにして試料17とした。 次に、上記試料17を誘電体とした誘電体共振器
の25℃の温度における比誘電率εと無負荷のQを
測定した試験方法とその結果について説明する。 まず、予め前述の試料17の直径Dをマイクロメ
ータで測定した後、横河ヒユーレツトパツカード
社製の8620Aスイープオシレーダ、8410Aネツト
ワークアナライザ、8743Aテストユニツト及びコ
ンピユータからなる測定システムを用い、比誘電
率εと無負荷のQを測定した。 上記テストユニツトには、誘電体共振器の電極
用金属端板(直径24mm、厚さ3mm)2枚が含まれ
ており、まずこれら金属端板で上記試料3が挟ま
れ、誘電体共振器が構成される。次にこの共振器
の共振周波数0と共振時の挿入損dBが測定され
る。そしてこの共振時の挿入損dBの測定値と、
予め実測された上記試料17+++D、厚さtがコ
ンピユータに入力されることによつて、供試用誘
電体共振器の比誘電率εと無負荷のQがそれぞれ
演算され、その結果が打ち出される。 上記測定システムにおいて求められる比誘電率
εは、コンピユータのプログラムに従つて、πD、
共振波長λ0=C/f0、伝搬波長λg=2t、第2種ベ
ツセル関数v2=(πD/λ0)〔(λ0/λg)2−1〕、

1種ベツセル関数u2が測定または計算され、これ
らの値からε=(λ0/πD)2(u2+v2)+1なる演算
式で求められる。また、無負荷のQは、やはりコ
ンピユータプログラムに従い、負荷QL=f0/f2
f1(電力半値幅)、at=10-ILo/20が求めら、これら
の値からQ=QL/1−atなる演算式で求められ
る。 前述のようにして求められた20個の試料の比誘
電率εの平均値は29.8、最大値は29.5、最小値は
30.2であつた。また、試料20個の無負荷のQの平
均値は12000、最大値は13600、最小値は11200で
あつた。これら平均値を、上記組成式のxの値、
焼成温度FTと共に下表の試料番号17の欄に示し
た。 さらに、下表における試料番号17以外の試料1
〜16及び18〜24の誘電体磁器組成物につい
ても、それぞれの組成に応じて焼成温度FTが多
少異なつた他は、前述した試料17と同様の方法で
供試用誘電体共振器を作り、上記と同じ方法でそ
れぞれの共振器の各特性を求めた。これらの特性
の平均値と焼成温度FTを下表の該当欄に示した。
[Industrial Application Field] The present invention relates to a dielectric ceramic composition for a dielectric resonator having a resonance frequency of 10-odd GHz. [Prior Art] A dielectric resonator with a resonant frequency of 10-odd GHz has an excellent no-load Q of about 10,000. The dielectric of this conventional dielectric resonator contains Ba・[Zn 1/3
A dielectric ceramic composition expressed by the composition formula Ta 2/3 .[Zn 1/3 Nb 2/3 ] 1 /3.O 3 was used. [Problems to be Solved by the Invention] The conventional dielectric ceramic compositions described above are expensive. The reason for this is that the firing temperature during the manufacturing process is approximately
Because the temperature is as high as 1,600℃, equipment costs for the kiln, its repair costs, and thermal energy costs increase.
This is because these increase manufacturing costs.
Therefore, there is a need for a dielectric ceramic composition that can be fired at lower temperatures. This invention was devised based on the above-mentioned demand, and provides a dielectric ceramic composition that is cheaper than conventional compositions. [Means for Solving the Problems] The dielectric ceramic composition of the present invention that achieves the above object has Ba.[Mg (x) Co (1-x ) 1/3 ] x)2/
The main component is a composite perovskite in which x in the composition formula expressed by 3.O3 is in the range of 0.3 to 0.9, and this 100
It contains 0.01 to 0.5 parts by weight of one or more components from the group Al 2 O 3 , Cr 2 O 3 , Y 2 O 3 and Mn 2 O 3 based on the weight part. [Example] Next, the value of x in the above composition formula is 0.5.
Ba・(Mg 0.5 Co 0.5 ) 1/3・(Ta 0.5 Nb 0.5 ) 2/3・O 3 components are
A method for producing a dielectric ceramic composition containing 100 parts by weight and 0.1 parts by weight of Cr 2 O 3 will be described. First, 98.67 g of BaCO 3 powder (equivalent to 0.500 mol),
MgO powder 3.36g (equivalent to 0.083 mol), CoO powder
6.22g (equivalent to 0.083 moles), 36.18g of Ta 2 O 5 powder
(equivalent to 0.083 mol), 22.06 g of Nb 2 O 5 powder (equivalent to 0.083 mol) and 0.167 g of Cr 2 O 3 powder (equivalent to the above BaCO 3
Based on 100 parts by weight of the total amount of components from Nb 2 O 5 to
(equivalent to 0.1 part by weight) was weighed. This weighed powder was placed in a ball mill with pure water and wet mixed for 24 hours. The mixture thus obtained was dehydrated and dried at a temperature of 150°C for 5 hours, and then calcined at a temperature of 1100°C for 2 hours. Next, the calcined product was ground in a ball mill. Add polyvinyl alcohol to this crushed material.
3.0g was added, mixed using a grinder, and granulated by passing through a 60-mesh sieve. 0.66 of these granules
g was placed in a mold and a pressure of 3 tons/cm 2 was applied. By repeating this pressure molding, a diameter of 7.0mmφ,
We made 20 disks with a thickness of 3.5 mm. These disks were then fired at a temperature of 1,370°C for 4 hours to a diameter of approx.
A dielectric ceramic disk of 6.0 mm and approximately 3.1 mm in thickness was obtained. Lap polish both sides of these dielectric porcelain discs,
Sample 17 was obtained by setting the thickness t to 3.00 mm. Next, a test method and results for measuring the relative dielectric constant ε at a temperature of 25° C. and the no-load Q of a dielectric resonator using the sample 17 as a dielectric will be explained. First, after measuring the diameter D of the aforementioned sample 17 with a micrometer, using a measurement system consisting of an 8620A sweep oscillator, an 8410A network analyzer, an 8743A test unit, and a computer manufactured by Yokogawa Heuretsu Patscard Co., Ltd. The relative permittivity ε and the no-load Q were measured. The above test unit includes two metal end plates (diameter 24 mm, thickness 3 mm) for electrodes of the dielectric resonator. First, the sample 3 is sandwiched between these metal end plates, and the dielectric resonator is configured. Next, the resonant frequency 0 of this resonator and the insertion loss dB at resonance are measured. And the measured value of insertion loss dB at this resonance,
By inputting the sample 17+++D and the thickness t, which were actually measured in advance, into a computer, the dielectric constant ε and the unloaded Q of the dielectric resonator under test are respectively calculated, and the results are output. The relative dielectric constant ε determined in the above measurement system is determined by πD,
Resonance wavelength λ 0 =C/f 0 , propagation wavelength λg = 2t, Bessel function of the second kind v 2 = (πD/λ 0 ) [(λ 0 /λg) 2 −1],
The Betzel function of the first kind u 2 is measured or calculated, and is determined from these values using the formula ε=(λ 0 /πD) 2 (u 2 +v 2 )+1. Also, the no-load Q is calculated as follows according to the computer program: load Q L = f 0 / f 2
f 1 (power width at half maximum) and a t =10 −ILo/20 are obtained, and from these values, it is obtained using the arithmetic expression Q=Q L /1− at . The average value of the dielectric constant ε of the 20 samples determined as described above is 29.8, the maximum value is 29.5, and the minimum value is
It was 30.2. Furthermore, the average value of the unloaded Q of the 20 samples was 12,000, the maximum value was 13,600, and the minimum value was 11,200. These average values are calculated as the value of x in the above composition formula,
It is shown in the column of sample number 17 in the table below along with the firing temperature FT. Furthermore, sample 1 other than sample number 17 in the table below
Regarding the dielectric ceramic compositions Nos. 16 and 18 through 24, test dielectric resonators were made in the same manner as for Sample 17 described above, except that the firing temperature FT was slightly different depending on each composition. The characteristics of each resonator were determined using the same method as described above. The average values of these properties and the firing temperature FT are shown in the relevant columns of the table below.

【表】【table】

〔発明の効果〕〔Effect of the invention〕

以上説明した通り、この発明の誘電体磁器組成
物は、従来のものとほゞ同等の特性が得られた上
で、製造過程の焼成温度FTを1370〜1400℃と低
くすることができるため、焼成炉等の設備面や、
焼成のための熱エネルギ等の点から、従来の誘電
体磁器組成物に比較して安価な誘電体磁器組成物
が得られる。具体的には、焼結のため1600℃の焼
成温度FTを必要とする従来の誘電体磁器組成物
に比べて、約15%の原価低減が見込まれる。
As explained above, the dielectric ceramic composition of the present invention can obtain properties almost equivalent to those of conventional compositions, and can lower the firing temperature FT during the manufacturing process to 1370-1400°C. Equipment such as firing furnaces,
In terms of thermal energy for firing, etc., a dielectric ceramic composition can be obtained that is cheaper than conventional dielectric ceramic compositions. Specifically, the cost is expected to be reduced by about 15% compared to conventional dielectric ceramic compositions that require a firing temperature FT of 1600°C for sintering.

Claims (1)

【特許請求の範囲】 1 Ba・〔Mg(x)Co(1-x1/3・〔Ta(x)Nb(1-x)2/3
O3で表される組成式のxが0.3〜0.9の範囲である
成分が100重量部と、Al2O3、Cr2O3、Y2O3
Mn2O3のグループの一種以上の成分が0.01〜0.5
重量部とからなる誘電体磁器組成物。
[Claims] 1 Ba・[Mg (x) Co (1-x )] 1/3・[Ta (x) Nb (1-x) ] 2/3
100 parts by weight of a component whose compositional formula represented by O 3 has x in the range of 0.3 to 0.9, Al 2 O 3 , Cr 2 O 3 , Y 2 O 3 ,
One or more components of the Mn 2 O 3 group are 0.01 to 0.5
A dielectric ceramic composition consisting of parts by weight.
JP60093426A 1985-04-30 1985-04-30 Dielectric ceramic composition Granted JPS61253710A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60093426A JPS61253710A (en) 1985-04-30 1985-04-30 Dielectric ceramic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60093426A JPS61253710A (en) 1985-04-30 1985-04-30 Dielectric ceramic composition

Publications (2)

Publication Number Publication Date
JPS61253710A JPS61253710A (en) 1986-11-11
JPH0515006B2 true JPH0515006B2 (en) 1993-02-26

Family

ID=14081974

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60093426A Granted JPS61253710A (en) 1985-04-30 1985-04-30 Dielectric ceramic composition

Country Status (1)

Country Link
JP (1) JPS61253710A (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS63265811A (en) * 1987-04-21 1988-11-02 Ube Ind Ltd Manufacture of feedstock powder of easily sinterable perovskite composite oxide
JP2000249561A (en) * 1999-03-03 2000-09-14 Matsushita Electric Ind Co Ltd Angular velocity sensor

Also Published As

Publication number Publication date
JPS61253710A (en) 1986-11-11

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