JP3205029B2 - High frequency dielectric ceramic composition - Google Patents

High frequency dielectric ceramic composition

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Publication number
JP3205029B2
JP3205029B2 JP03102592A JP3102592A JP3205029B2 JP 3205029 B2 JP3205029 B2 JP 3205029B2 JP 03102592 A JP03102592 A JP 03102592A JP 3102592 A JP3102592 A JP 3102592A JP 3205029 B2 JP3205029 B2 JP 3205029B2
Authority
JP
Japan
Prior art keywords
composition
dielectric ceramic
ceramic composition
dielectric
high 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 - Fee Related
Application number
JP03102592A
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Japanese (ja)
Other versions
JPH05225825A (en
Inventor
島 暢 小
見 通 昭 鶴
藤 一 明 遠
Original Assignee
エフ・ディ−・ケイ株式会社
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Priority to JP03102592A priority Critical patent/JP3205029B2/en
Publication of JPH05225825A publication Critical patent/JPH05225825A/en
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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】本発明は新規な高周波用誘電体磁
器組成物に関するものである。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a novel high frequency dielectric ceramic composition.

【0002】[0002]

【従来の技術と解決しようとする課題】誘電体磁器組成
物は、たとえばマイクロ波やミリ波等の高周波領域にお
いて誘電体共振器やMIC用誘電体基板等に利用されて
いる。このような誘電体磁器組成物としては従来から、
たとえばBa(Zn1/3 ,Ta2/3 )O−Ba(Zn
1/3 ,Nb2/3 )Oの系がよく知られており、最近B
a(Zr,Zn,Ta)O7/2-x/2-3y/2の系やB
a(SnZnTa)O7/2-x/2-3y/2の系が開発さ
れている(特開昭58−45155,58−45156
号公報)。
2. Description of the Related Art Dielectric ceramic compositions are used in dielectric resonators, MIC dielectric substrates, and the like in high-frequency regions such as microwaves and millimeter waves. Conventionally, as such a dielectric porcelain composition,
For example, Ba (Zn1 / 3, Ta2 / 3) O 3 -Ba (Zn
1/3, Nb2 / 3) system of O 3 are well known, recently B
a (Zr x , Zn y , T az ) O 7 / 2-x / 2-3y / 2 or B
The system of a (Sn x Zn y Ta z ) O 7/2-x / 2-3y / 2 have been developed (JP-58-45155,58-45156
No.).

【0003】更にBa組成比を化学量論比よりも不足さ
せた誘電体磁器組成物も提案されている(特開平2−5
1464号公報)。この組成物は一般式Ba1-x (Zn
1/3Ta2/3 )Oで表わされ0.004≦x≦0.0
1の範囲内となるよう秤量し、仮焼き後乾式法のみによ
って粉砕し、成形後1600〜1700℃で1〜10時
間焼成することによって製造されている。この方法によ
るときは短時間に少ないエネルギーでQ値の高い組成物
がえられている。
Further, a dielectric ceramic composition in which the Ba composition ratio is less than the stoichiometric ratio has been proposed (Japanese Patent Laid-Open No. 2-5 / 1990).
No. 1464). This composition has the general formula Ba 1-x (Zn
It is represented by 1 / 3Ta2 / 3) O 3 0.004 ≦ x ≦ 0.0
It is manufactured by weighing so as to fall within the range of 1, pulverizing only by a dry method after calcining, and firing after molding at 1600 to 1700 ° C. for 1 to 10 hours. According to this method, a composition having a high Q value is obtained in a short time with little energy.

【0004】上記のマイクロ波誘電体共振器等で使用す
る材料としては高いQ値を維持しつつ共振周波数の温度
係数(τf )を再現性良く任意の値に設定できることが
望まれる。最近では使用する周波数領域が高くなってき
ておりQ値の不足が生じてきている。
It is desired that the material used in the above-mentioned microwave dielectric resonator or the like can set the temperature coefficient (τ f ) of the resonance frequency to an arbitrary value with good reproducibility while maintaining a high Q value. Recently, the frequency range to be used has been increasing, and shortage of the Q value has occurred.

【0005】かくて本発明は上記ような技術的課題を解
消し、さらに高い周波数領域で使用可能な高いQ値を有
し、且つ共振周波数温度領域を再現性良く設定できる高
周波用誘電体磁器組成物を提供することを目的とするも
のである。
Thus, the present invention solves the above-mentioned technical problems, and further has a high Q value usable in a high frequency range and a high frequency dielectric ceramic composition capable of setting the resonance frequency temperature range with good reproducibility. The purpose is to provide things.

【0006】[0006]

【課題を解決するための手段】本発明者の研究、実験に
よれば、従来用いられているBa(Zn1/3 Ta2/3 )
系材料の一部をBaZrO系材料及びBaSnO
系材料で置換し、しかもBa組成比を化学量論比より
も不足した状態にすることにより、上記目的が達成さ
れ、共振周波数温度係数を再現性良く調整可能とし、更
にQ値の高い誘電体磁器組成物を得ることができること
を見出して本発明に到ったものである。
According to the research and experiments of the present inventors, Ba (Zn1 / 3 Ta2 / 3) which has been conventionally used is used.
A part of the O 3 -based material is made of BaZrO 3 -based material and BaSnO
By substituting with a tertiary material and making the Ba composition ratio less than the stoichiometric ratio, the above object is achieved, the temperature coefficient of resonance frequency can be adjusted with good reproducibility, and a dielectric material having a high Q value can be obtained. The inventors have found that a body porcelain composition can be obtained, and arrived at the present invention.

【0007】よって本発明は、一般式 (1−x−y)Ba1-z (Zn1/3 Ta2/3 )O+x
Ba1-z ZrO+yBa1-z SnO で表わされ、0.002≦x≦0.05、0.002≦
y≦0.08、0.005≦z≦0.050の範囲であ
ることを特徴とする高周波用誘電体磁器組成物を提供す
るものである。
Accordingly, the present invention relates to a compound of the general formula (1-xy) Ba 1-z (Zn1 / 3Ta2 / 3) O 3 + x
Represented by Ba 1-z ZrO 3 + yBa 1-z SnO 3, 0.002 ≦ x ≦ 0.05,0.002 ≦
An object of the present invention is to provide a dielectric ceramic composition for high frequencies, wherein y ≦ 0.08 and 0.005 ≦ z ≦ 0.050.

【0008】本発明の磁器組成物は上記のような組成を
有するものであり、ここでzの値を0.005≦z≦
0.05の範囲としたのは、zが0.005以下では焼
結しにくく、zが0.05以上では亀裂が入りやすいた
めであり、zの範囲を上記値に保つことによってこれら
の問題を回避することができる。
[0008] The porcelain composition of the present invention has the above composition, where the value of z is 0.005 ≦ z ≦
The reason for setting the range to 0.05 is that if z is 0.005 or less, sintering is difficult, and if z is 0.05 or more, cracks are likely to occur. Can be avoided.

【0009】又本発明では前記のようにBa(Zn1/3
Ta2/3 )Oの一部をBaZrOとBaSnO
置換したのであるがBaZrOによる置換は共振周波
数温度係数(τf )の増加をもたらし、Ba1-z SnO
による置換は共振周波数温度係数の減少とQ値の向上
をもたらすため両者の置換量即ち上式の中xとyの値を
上記範囲内で最適化を図ることによって高いQ値を維持
しつつ共振周波数温度係数を任意の好適な値に設定する
ことができ、近年高まっている高い周波数領域において
も良好に使用しうるようになったのである。
In the present invention, as described above, Ba (Zn1 / 3
Ta2 / 3) substituted but is was replaced with BaZrO 3 and BaSnO 3 by BaZrO 3 a part of the O 3 will result in an increase in the resonant frequency temperature coefficient (τ f), Ba 1- z SnO
Since the replacement by 3 results in a decrease in the resonance frequency temperature coefficient and an improvement in the Q value, the replacement amount of the two, that is, the values of x and y in the above equation are optimized within the above range, thereby maintaining a high Q value. The temperature coefficient of the resonance frequency can be set to any suitable value, so that it can be used favorably even in the high frequency range that has been increasing in recent years.

【0010】今上記一般式を有する本発明の三成分系誘
電体磁器組成物の組成範囲を三角図表で示せば図1のと
おりである。
FIG. 1 is a triangular chart showing the composition range of the ternary dielectric ceramic composition of the present invention having the above general formula.

【0011】このような誘電体磁器組成物を次のような
方法によって製造し、えられた組成物の誘電特性を測定
した。出発原料として高純度のBaCO、ZnO、T
、ZrO、SnOを用い、これらを上記一
般式に示される組成になるように原料を秤量した。これ
を樹脂ポットで純水と共に20時間湿式混合した後乾燥
し、1300℃において10時間の仮焼を行なった。え
られた仮焼品を乳鉢で粉砕し、バインダーを加えて造粒
した。これを30MPa の圧力で直径16mm、厚さ9mmの
円板に成型した。次いでこの成型品を大気中において1
600℃、40時間焼成して目的とする誘電体磁器組成
物を得た。
[0011] Such a dielectric ceramic composition was manufactured by the following method, and the dielectric properties of the obtained composition were measured. High purity BaCO 3 , ZnO, T as starting materials
Using a 2 O 5 , ZrO 2 , and SnO 2 , raw materials were weighed so as to have a composition represented by the above general formula. This was wet-mixed with pure water in a resin pot for 20 hours, dried, and calcined at 1300 ° C. for 10 hours. The obtained calcined product was pulverized in a mortar and granulated by adding a binder. This was molded into a disk having a diameter of 16 mm and a thickness of 9 mm under a pressure of 30 MPa. Next, the molded product is placed in the atmosphere for 1 hour.
It was fired at 600 ° C. for 40 hours to obtain a desired dielectric ceramic composition.

【0012】えられたこの組成物の成型品の上下面及び
側面を夫々1mm程度削りとって測定用の試料とし、この
試料について共振周波数約7GHz における比誘電率
εr 、誘電損失Qo 、共振周波数温度係数τf (ppm /
℃)をポストレゾネーター法により測定した。
The upper and lower surfaces and side surfaces of a molded article of the obtained composition are each shaved by about 1 mm to prepare a sample for measurement. The sample has a relative dielectric constant ε r , a dielectric loss Q o at a resonance frequency of about 7 GHz, and a resonance loss. Frequency temperature coefficient τ f (ppm /
° C) was measured by the post-resonator method.

【0013】今zを一定にしてx,yの値を変えてつく
られた上記一般式の三成分系組成物の比誘電率Er、誘
電損失Q、共振周波数温度係数τf (ppm /℃)を測定
して、組成の変化による各種誘電特性の変化を夫々順に
図2,3,4に示す。これらの図により本発明に係る三
成分系の誘電体磁器組成物は本発明の範囲外の組成物に
比してすぐれた誘電特性を有することが明らかであろ
う。
Now, the relative dielectric constant Er, the dielectric loss Q, and the resonance frequency temperature coefficient τ f (ppm / ° C.) of the ternary composition represented by the above general formula, which are made by changing the values of x and y while keeping z constant. Are measured, and changes in various dielectric properties due to changes in the composition are shown in FIGS. It will be apparent from these figures that the ternary dielectric ceramic composition according to the present invention has better dielectric properties than compositions outside the scope of the present invention.

【0014】[0014]

【発明の効果】上記のように、本発明に従ってBa(Z
n1/3 Ta2/3 )Oの一部をBaZrOとBaSn
系材料で置換し、Ba組成比を化学量論よりも不足
した状態にしてなる誘電体磁器組成物は高いQ値を維持
しつつ共振周波数温度係数をよく調整して任意の値に設
定することができ、高い周波数領域によく使用できて誠
に有効である。
As described above, according to the present invention, Ba (Z
n1 / 3 Ta2 / 3) BaZrO 3 a part of the O 3 and BaSn
The dielectric porcelain composition replaced with an O 3 -based material and having a Ba composition ratio less than the stoichiometry is set to an arbitrary value by well adjusting the resonance frequency temperature coefficient while maintaining a high Q value. It can be used well in the high frequency range and is really effective.

【図面の簡単な説明】[Brief description of the drawings]

【図1】本発明の組成物の組成範囲を示す三角図表。FIG. 1 is a triangular chart showing the composition range of the composition of the present invention.

【図2】本発明の組成物の組成の変化による比誘電率
(Er)の変化を示すグラフ。
FIG. 2 is a graph showing a change in relative dielectric constant (Er) according to a change in the composition of the composition of the present invention.

【図3】同誘電損失(Q)の変化を示すグラフ。FIG. 3 is a graph showing a change in dielectric loss (Q).

【図4】同共振周波数温度係数(τf )の変化を示すグ
ラフ。
FIG. 4 is a graph showing a change in the resonance frequency temperature coefficient (τ f ).

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭58−45156(JP,A) 特開 平2−199052(JP,A) (58)調査した分野(Int.Cl.7,DB名) H01B 3/12 C04B 35/00 ──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-58-45156 (JP, A) JP-A-2-199052 (JP, A) (58) Fields investigated (Int. Cl. 7 , DB name) H01B 3/12 C04B 35/00

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】一般式 (1−x−y)Ba1-z (Zn1/3 Ta2/3 )O+x
Ba1-z ZrO+yBa1-z SnO で表わされ、0.002≦x≦0.05、0.002≦
y≦0.08、0.005≦z≦0.050の範囲であ
ることを特徴とする高周波用誘電体磁器組成物。
1. The formula (1-xy) Ba 1 -z (Zn1 / 3 Ta2 / 3) O 3 + x
Represented by Ba 1-z ZrO 3 + yBa 1-z SnO 3, 0.002 ≦ x ≦ 0.05,0.002 ≦
A dielectric ceramic composition for high frequencies, wherein y ≦ 0.08 and 0.005 ≦ z ≦ 0.050.
JP03102592A 1992-02-18 1992-02-18 High frequency dielectric ceramic composition Expired - Fee Related JP3205029B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP03102592A JP3205029B2 (en) 1992-02-18 1992-02-18 High frequency dielectric ceramic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP03102592A JP3205029B2 (en) 1992-02-18 1992-02-18 High frequency dielectric ceramic composition

Publications (2)

Publication Number Publication Date
JPH05225825A JPH05225825A (en) 1993-09-03
JP3205029B2 true JP3205029B2 (en) 2001-09-04

Family

ID=12319981

Family Applications (1)

Application Number Title Priority Date Filing Date
JP03102592A Expired - Fee Related JP3205029B2 (en) 1992-02-18 1992-02-18 High frequency dielectric ceramic composition

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JP (1) JP3205029B2 (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5526617B2 (en) * 2008-08-07 2014-06-18 株式会社村田製作所 Dielectric ceramic and multilayer ceramic capacitors

Also Published As

Publication number Publication date
JPH05225825A (en) 1993-09-03

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