JPS6272558A - Dielectric ceramic composition - Google Patents

Dielectric ceramic composition

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Publication number
JPS6272558A
JPS6272558A JP60212669A JP21266985A JPS6272558A JP S6272558 A JPS6272558 A JP S6272558A JP 60212669 A JP60212669 A JP 60212669A JP 21266985 A JP21266985 A JP 21266985A JP S6272558 A JPS6272558 A JP S6272558A
Authority
JP
Japan
Prior art keywords
dielectric
ceramic composition
dielectric ceramic
present
mol
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
Application number
JP60212669A
Other languages
Japanese (ja)
Other versions
JPH0568426B2 (en
Inventor
鬼頭 良造
有馬 安孝
昌孝 藤永
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.)
Ube Corp
Original Assignee
Ube Industries 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 Ube Industries Ltd filed Critical Ube Industries Ltd
Priority to JP60212669A priority Critical patent/JPS6272558A/en
Publication of JPS6272558A publication Critical patent/JPS6272558A/en
Publication of JPH0568426B2 publication Critical patent/JPH0568426B2/ja
Granted legal-status Critical Current

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Abstract

(57)【要約】本公報は電子出願前の出願データであるた
め要約のデータは記録されません。
(57) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 〔産業上の利用分野〕 本発明の誘電体磁器組成物は、誘電体共振器材料の外に
、たとえばマイクロ波IC用誘電体基板。
DETAILED DESCRIPTION OF THE INVENTION [Industrial Application Field] The dielectric ceramic composition of the present invention can be used not only as a dielectric resonator material but also as a dielectric substrate for microwave ICs, for example.

誘電体調整棒等にも適用される。It is also applied to dielectric adjustment rods, etc.

〔従来技術およびその問題点〕[Prior art and its problems]

近年、マイクロ波回路の集積化に伴い、小型で高性能の
誘電体共振器が求められている。
In recent years, with the increasing integration of microwave circuits, there has been a demand for small, high-performance dielectric resonators.

このような誘電体共振器に使用される誘電体磁器組成物
には、比誘電率ε1が大きいこと、iた。
The dielectric ceramic composition used in such a dielectric resonator has a large relative dielectric constant ε1.

共振周波数の温度係数τfの安定度および共振周波数の
温度特性の直線性が優れ、無負荷Qが大きい共振器を構
成できること等の特性が要求されている。このような誘
電体磁器組成物として、従来TlO2およびBaO−T
iO2を主成分とするものが一般的であるが、誘電率の
温度係数が大きかったシマイクロ波帯域で損失が大きい
など問題があった。
Characteristics such as excellent stability of the temperature coefficient τf of the resonant frequency and linearity of the temperature characteristic of the resonant frequency, and the ability to construct a resonator with a large no-load Q are required. Conventionally, TlO2 and BaO-T are used as such dielectric ceramic compositions.
Those containing iO2 as a main component are common, but they have problems such as large loss in the microwave band where the temperature coefficient of dielectric constant is large.

この改良系として例えばB a O−T i Oz −
N d 203を主102003号公報にはB a O
−T i O2−N d 203に。
As this improved system, for example, B a O-T i Oz −
N d 203 is B a O in the main publication No. 102003.
-T i O2-N d 203.

微量のBi2O3を添加物として加え無負荷Qを改善し
た誘電体共振器材料が提案されているが共振周波数の温
度係数を十分小さい値(例えばτf≦10ppm/”C
)に調製することができないなど実用化するには困難な
面がある。
A dielectric resonator material has been proposed in which a trace amount of Bi2O3 is added as an additive to improve the no-load Q.
), which makes it difficult to put it into practical use.

一方最近ではv B a (M fy ・T a H)
 O3やBa(ZnKTa2,4)03. Ba(Zn
34”bz、g)Os系のペロブスカイト構造を持った
誘電体磁器が知られている。しかしながら、これらの材
料では誘電率(el−=25〜40)が小さいために共
振器を十分に小型化することができない難点がある。
On the other hand, recently v B a (M fy ・T a H)
O3 and Ba(ZnKTa2,4)03. Ba(Zn
34"bz, g) Os-based dielectric ceramics with a perovskite structure are known. However, these materials have a small dielectric constant (el-=25 to 40), so it is difficult to miniaturize the resonator sufficiently. There is a drawback that it cannot be done.

本発明の目的は、誘電体共振器材料、特に0.1〜4 
GHz帯で使用される誘電体共振器材料として好適な誘
電体磁器組成物を提供することにある。
The object of the present invention is to provide dielectric resonator materials, in particular 0.1-4
An object of the present invention is to provide a dielectric ceramic composition suitable as a dielectric resonator material used in the GHz band.

更に本発明の目的は、高誘電率でQが大きく。Furthermore, the object of the present invention is to have a high dielectric constant and a large Q.

τfの安定性がよく、シかも温度特性の直線性が良好な
誘電体磁器組成物を提供することにある。
The object of the present invention is to provide a dielectric ceramic composition having good stability of τf and good linearity of temperature characteristics.

本発明の目的は。The purpose of the present invention is to:

組成式 %式% (式中、Xは0.1〜0,2.yは0.5〜0.8.Z
は0.1〜0.2で、x+y+z=1であり、tは0.
1〜0.2である。) で表わされるバリウム、チタン、ネオジウム、ビスマス
および酸素からなる誘電体磁器組成物によって達成され
る。
Composition formula % formula % (wherein, X is 0.1-0, 2.y is 0.5-0.8.Z
is 0.1 to 0.2, x+y+z=1, and t is 0.
It is 1 to 0.2. ) is achieved by a dielectric ceramic composition consisting of barium, titanium, neodymium, bismuth and oxygen.

本発明は、 Bad、 TiO2およびNd2 o3を
主成分とし、特に従来の磁器組成物より多量にBiO%
を含有させたことによって、すなわち上記組成式におい
てX+7+Zを1モルとし、これにB10yを0.1〜
0.2モル含有させたことによって、共振周波数の温度
係数を10 ppm/ ’C以下にすることができ9本
発明の前記目的達成が可能になる。
The present invention contains Bad, TiO2 and Nd2o3 as main components, and in particular contains a larger amount of BiO% than conventional porcelain compositions.
In other words, in the above compositional formula, X+7+Z is set to 1 mol, and B10y is added to this by 0.1 to 1 mole.
By containing 0.2 mol, the temperature coefficient of the resonance frequency can be made 10 ppm/'C or less, making it possible to achieve the above-mentioned object of the present invention.

本発明による誘電体磁器組成物は、大きな比誘電率を有
するとともに、共振器を構成した時の無負荷Qの値も大
きくなる。さらに、安定した共振周波数の温度特性を有
し、特に−40゛C〜60°Cにおける温度特性が良好
な直線性を有する。
The dielectric ceramic composition according to the present invention has a large dielectric constant, and also has a large no-load Q value when forming a resonator. Furthermore, it has a stable temperature characteristic of a resonant frequency, and particularly has good linearity in the temperature characteristic at -40°C to 60°C.

〔実施例〕〔Example〕

以下2本発明の実施例を詳細に説明する。 Two embodiments of the present invention will be described in detail below.

本発明による誘電体磁器組成物は、バリウム。The dielectric ceramic composition according to the present invention is made of barium.

チタン、ネオジウム、ビスマス等の炭酸塩、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。
It can be manufactured by a method in which starting materials such as carbonates and oxides of titanium, neodymium, bismuth, etc. are mixed and calcined, then shaped, fired, and sintered.

まず、炭酸バリウム、酸化チタン、酸化ネオジウムおよ
び酸化ビスマスを各所定量ずつ水、アルコール等の溶媒
と共に湿式混合する。続いて、水。
First, predetermined amounts of each of barium carbonate, titanium oxide, neodymium oxide, and bismuth oxide are wet-mixed with a solvent such as water and alcohol. Next, water.

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900〜1100°Cで約
5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100〜1000 Kg/−)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1300〜1
450°Cで焼成すれば、上記誘電体磁器組成物が得ら
れる。
After removing alcohol and the like, it is pulverized and calcined at 900 to 1100°C for about 5 hours in an oxygen-containing gas atmosphere (for example, air atmosphere). The calcined product thus formed is pulverized, then mixed with an organic binder such as polyvinyl alcohol to make it homogeneous, dried, pulverized, and pressure-molded (at a pressure of 100 to 1000 Kg/-). Then, this molded product is placed in an oxygen-containing gas atmosphere such as air at a temperature of 1,300 to 1
By firing at 450°C, the above dielectric ceramic composition can be obtained.

こうして得られた誘電体磁器組成物は、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ことで、
誘電体共振器、マイクロ技工C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、特に0.1〜
4 GHz帯で使用される誘電体共振器としたときにす
ぐれた効果が奏される。
The dielectric ceramic composition thus obtained can be used as is or by processing it into an appropriate shape and size as necessary.
It can be used as a material for dielectric resonators, dielectric substrates for micro technology C, dielectric adjustment rods, etc.
Excellent effects can be achieved when used as a dielectric resonator used in the 4 GHz band.

〔実施例1〕 炭酸バリウム(BaCO3)粉末0.15モル、酸化チ
タン粉末(Ti02 )0.70モル、酸化ネオジウム
粉末(Nd203)  0.15モルおよび酸化ビスマ
ス粉末(Bi03A) 0.10モルをエタノールと共
にボールミルに入れ、10時時間式混合した。この混合
物をボールミルから取シ出して溶媒のエタノールを蒸発
させ、らい潰損で1時間粉砕した。粉砕物は、空気雰囲
気下に950°Cで仮焼した後、再びらい潰損で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15mJL厚さ5.
5mのペレットに成形して空気雰囲気下に1360°C
で2時間焼成。
[Example 1] 0.15 mol of barium carbonate (BaCO3) powder, 0.70 mol of titanium oxide powder (Ti02), 0.15 mol of neodymium oxide powder (Nd203) and 0.10 mol of bismuth oxide powder (Bi03A) were added to ethanol. The mixture was placed in a ball mill and mixed for 10 hours. The mixture was taken out from the ball mill, the solvent ethanol was evaporated, and the mixture was ground for 1 hour using a millstone. The pulverized product was calcined at 950°C in an air atmosphere, and then pulverized again using a leprosy crusher for 1 hour. After adding an appropriate amount of polyvinyl alcohol solution and mixing uniformly, this pulverized product has a diameter of 15 mJL and a thickness of 5.5 m.
Formed into 5m pellets and heated at 1360°C in an air atmosphere.
Bake for 2 hours.

焼結して本実施例の誘電体磁器組成物(0,15Ba0
・0.70T102・0.15Nd203・0.10B
iO%)を得た。
The dielectric ceramic composition of this example (0,15Ba0
・0.70T102・0.15Nd203・0.10B
iO%) was obtained.

こうして得られた実施例1の磁器組成物を直径9鰭グ、
厚さ31111!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f0 (2〜60Hz )
における無負荷Qおよび比誘電率ε、を求めた。また、
共振周波数の温度依存性については一40〜50°Cの
範囲で測定し温度係数τfを求めた。その結果を第1表
に示す。
The thus obtained porcelain composition of Example 1 was prepared with a diameter of 9 g,
Thickness 31111! After cutting to the size of
The no-load Q and relative dielectric constant ε were determined. Also,
The temperature dependence of the resonance frequency was measured in the range of -40 to 50°C, and the temperature coefficient τf was determined. The results are shown in Table 1.

〔実施例2〜5〕 実施例1の酸化ビスマス粉末(Bib、4) 0.10
モルを、 0.12モル(実施例2)、o、1sモル(
実施例3)、0.17モル(実施例4)および0620
モル(実施例5)にかえたほかは、実施例1と同様にし
て誘電体磁器組成物を製造し、同様にして特性を測定し
た。その結果を第1表に示す。
[Examples 2 to 5] Bismuth oxide powder (Bib, 4) of Example 1 0.10
mole, 0.12 mole (Example 2), o, 1 s mole (
Example 3), 0.17 mol (Example 4) and 0620
A dielectric ceramic composition was produced in the same manner as in Example 1, except that the molar ratio was changed to molar (Example 5), and the characteristics were measured in the same manner. The results are shown in Table 1.

〔比較例1〜4〕 実施例1の酸化ビスマス粉末(Bi○3/2)0.10
モルを、添加しなかった(比較例1)、o、o1モルに
かえた(比較例2)、0.02モルにかえた(比較例3
)および0.25モルにかえた(比較例4)ほかは、実
施例1と同様にし誘電体磁器組成物を製造し、同様にし
て特性を測定した。その結果を第1表に示す。
[Comparative Examples 1 to 4] Bismuth oxide powder of Example 1 (Bi○3/2) 0.10
The mole was not added (Comparative Example 1), o, o1 mole was changed (Comparative Example 2), and o was changed to 0.02 mole (Comparative Example 3).
) and 0.25 mol (Comparative Example 4), a dielectric ceramic composition was produced in the same manner as in Example 1, and its properties were measured in the same manner. The results are shown in Table 1.

第   1   表 ※A=0.15BaO−0,70Ti02−0.15N
d203〔発明の効果〕 本発明の誘電体磁器組成物は、高誘電率でQが大きく、
τfの安定性がよく、温度特性の直線性が良好であシ、
誘電体共撮器材料、特に0.1〜40H2帯で使用され
る共振器材料として好適である。
Table 1 *A=0.15BaO-0,70Ti02-0.15N
d203 [Effect of the invention] The dielectric ceramic composition of the present invention has a high dielectric constant and a large Q,
The stability of τf is good, the linearity of temperature characteristics is good,
It is suitable as a dielectric resonator material, especially as a resonator material used in the 0.1 to 40H2 band.

Claims (1)

【特許請求の範囲】 組成式 xBaO・yTiO_2・zNd_2O_3・tBiO
_3_/_2(式中、xは0.1〜0.2、yは0.5
〜0.8、zは0.1〜0.2で、x+y+z=1であ
り、tは0.1〜0.2である。) で表わされるバリウム、チタン、ネオジウム、ビスマス
および酸素からなる誘電体磁器組成物。
[Claims] Compositional formula xBaO・yTiO_2・zNd_2O_3・tBiO
_3_/_2 (in the formula, x is 0.1 to 0.2, y is 0.5
~0.8, z is 0.1-0.2, x+y+z=1, and t is 0.1-0.2. ) A dielectric ceramic composition consisting of barium, titanium, neodymium, bismuth and oxygen.
JP60212669A 1985-09-27 1985-09-27 Dielectric ceramic composition Granted JPS6272558A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60212669A JPS6272558A (en) 1985-09-27 1985-09-27 Dielectric ceramic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60212669A JPS6272558A (en) 1985-09-27 1985-09-27 Dielectric ceramic composition

Publications (2)

Publication Number Publication Date
JPS6272558A true JPS6272558A (en) 1987-04-03
JPH0568426B2 JPH0568426B2 (en) 1993-09-28

Family

ID=16626436

Family Applications (1)

Application Number Title Priority Date Filing Date
JP60212669A Granted JPS6272558A (en) 1985-09-27 1985-09-27 Dielectric ceramic composition

Country Status (1)

Country Link
JP (1) JPS6272558A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0701981A1 (en) 1994-08-30 1996-03-20 Ube Industries, Ltd. Dielectric ceramic composition

Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3775142A (en) * 1971-01-26 1973-11-27 Solid State Dielectrics Inc Improved ceramic compositions for high stability capacitors
JPS49120200A (en) * 1973-03-23 1974-11-16
JPS5520602A (en) * 1978-06-22 1980-02-14 Mitsubishi Electric Corp Dehydrator for sludge
JPS56102003A (en) * 1980-01-16 1981-08-15 Matsushita Electric Ind Co Ltd Porcelain for dielectric resonator
JPS57156367A (en) * 1981-03-23 1982-09-27 Tdk Electronics Co Ltd Dielectric ceramic composition
JPS599507A (en) * 1982-07-09 1984-01-18 Hitachi Ltd Device for measuring length of cast material
JPS6056306A (en) * 1983-09-06 1985-04-01 松下電器産業株式会社 Dielectric porcelain composition
JPS61215255A (en) * 1985-03-18 1986-09-25 京セラ株式会社 Dielectric ceramic composition

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3775142A (en) * 1971-01-26 1973-11-27 Solid State Dielectrics Inc Improved ceramic compositions for high stability capacitors
JPS49120200A (en) * 1973-03-23 1974-11-16
JPS5520602A (en) * 1978-06-22 1980-02-14 Mitsubishi Electric Corp Dehydrator for sludge
JPS56102003A (en) * 1980-01-16 1981-08-15 Matsushita Electric Ind Co Ltd Porcelain for dielectric resonator
JPS57156367A (en) * 1981-03-23 1982-09-27 Tdk Electronics Co Ltd Dielectric ceramic composition
JPS599507A (en) * 1982-07-09 1984-01-18 Hitachi Ltd Device for measuring length of cast material
JPS6056306A (en) * 1983-09-06 1985-04-01 松下電器産業株式会社 Dielectric porcelain composition
JPS61215255A (en) * 1985-03-18 1986-09-25 京セラ株式会社 Dielectric ceramic composition

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0701981A1 (en) 1994-08-30 1996-03-20 Ube Industries, Ltd. Dielectric ceramic composition
US5827792A (en) * 1994-08-30 1998-10-27 Ube Industries, Ltd. Dielectric ceramic composition

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JPH0568426B2 (en) 1993-09-28

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