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JPS6283364A - dielectric porcelain composition - Google Patents

dielectric porcelain composition

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Publication number
JPS6283364A
JPS6283364A JP60222864A JP22286485A JPS6283364A JP S6283364 A JPS6283364 A JP S6283364A JP 60222864 A JP60222864 A JP 60222864A JP 22286485 A JP22286485 A JP 22286485A JP S6283364 A JPS6283364 A JP S6283364A
Authority
JP
Japan
Prior art keywords
dielectric
mol
dielectric ceramic
ceramic composition
oxide powder
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
JP60222864A
Other languages
Japanese (ja)
Other versions
JPH0712971B2 (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 JP60222864A priority Critical patent/JPH0712971B2/en
Publication of JPS6283364A publication Critical patent/JPS6283364A/en
Publication of JPH0712971B2 publication Critical patent/JPH0712971B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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〕 本発明は、誘電体共振器材料として好適な。[Detailed description of the invention] [Industrial application field] The present invention is suitable as a dielectric resonator material.

BaO−Ti02−Ba0−Ti02−Nd203−、
(、WO3、YO3% )系の誘電体磁器組成物に関す
る。
BaO-Ti02-Ba0-Ti02-Nd203-,
(, WO3, YO3%) system dielectric ceramic composition.

本発明の誘電体磁器組成物は、誘電体共振器材料のほか
に9例えばマイクロ波IC用誘電体基板。
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使用することができる。It can also be used for 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、また。
The dielectric ceramic composition used in such a dielectric resonator has a large 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TiO2、BaO−TiO2等を主成分とする
ものが知られているが、温度係数が大きかったシ、マイ
クロ波帯域での誘電損失が大きかったりして実用化する
には困難な面がある。
Characteristics such as excellent stability of the temperature coefficient τf of the resonant frequency, excellent linearity of the temperature characteristic of the resonant frequency, and a large no-load Q are required. As such dielectric ceramic compositions, those mainly composed of TiO2, BaO-TiO2, etc. are known, but they have large temperature coefficients and large dielectric loss in the microwave band, so they are not practical. There are some aspects that are difficult to achieve.

またB a O−T i O2−N a203系の誘電
体磁器組成物についての提案CBor、 Dt、 Ke
ram、 Ges、 55(1978)Nr、7; 特
開昭60−35406号等〕もあるが、後記比較例1〜
4からも明らかであるように、Qが小さく、比誘電率に
ついても改良すべき点が残されている。
In addition, proposals for dielectric ceramic compositions based on B a O-T i O2-Na203 CBor, Dt, Ke
ram, Ges, 55 (1978) Nr, 7; JP-A No. 60-35406, etc.), but Comparative Examples 1-
As is clear from No. 4, Q is small and there is still room for improvement regarding the dielectric constant.

また最近ではBa(My3A−Taq) 03やBa 
(ZnH・Taq)o3゜Ba(ZnH・Nl)%)0
3系等のペロプスカイト型構造を有する誘電体磁器組成
物が提案されているが、比誘電率が小さい(ε、=25
〜40程度)ために。
Recently, Ba (My3A-Taq) 03 and Ba
(ZnH・Taq)o3゜Ba(ZnH・Nl)%)0
Dielectric ceramic compositions having a perovskite structure such as the 3-based dielectric ceramic composition have been proposed, but the dielectric constant is small (ε, = 25
~40 degrees) for.

例えば0.1〜4 GH2帯で使用される共振器とした
ときに、共振器を十分に小型化することができない難点
がある。
For example, when a resonator is used in the 0.1 to 4 GH2 band, there is a drawback that the resonator cannot be sufficiently miniaturized.

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、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.

〔問題点を解決するための手段および作用〕本発明は9
組成式 %式% (式中、MeはVOs  、 WO3およびWO3,よ
シなる群から選択された1種以上を示し* x+y+z
を1モルとしたとき又は0.1〜0.2モル、yは0.
5〜0.8モル、2は0.1〜0.2モルで、tはx+
y+z = 1モルに対して0.0003〜0.3モル
、好ましくはo、o o o s〜0.02モルである
。)で表わされるバナジウム、タングステンおよびイツ
トリウムよシなる群から選択された1種以上の元素、ネ
オジウム、チタン、バリウムおよび酸素からなる誘電体
磁器組成物に関するものである。
[Means and effects for solving the problems] The present invention has 9
Composition formula % Formula % (In the formula, Me represents one or more selected from the group consisting of VOs, WO3, and WO3 *x+y+z
is 1 mole or 0.1 to 0.2 mole, y is 0.
5 to 0.8 mol, 2 is 0.1 to 0.2 mol, t is x+
0.0003 to 0.3 mol, preferably o, o o s to 0.02 mol per y+z = 1 mol. ), neodymium, titanium, barium, and oxygen.

本発明は、特定量のBad、 TiO2およびNd2 
o3を主成分としt vo、  、vo3およびYOH
の1種以上を特定量含有させたことによって、従来の誘
電体磁器組成物の難点を改良することができるという知
見に基いている。
The present invention provides specific amounts of Bad, TiO2 and Nd2
With o3 as the main component, t vo, , vo3 and YOH
This is based on the knowledge that the drawbacks of conventional dielectric ceramic compositions can be improved by containing a specific amount of one or more of the following.

本発明において、■oSA、W03およびY03A  
は共通して無負荷Qを大きく向上させる作用を有してお
シ、比誘電率も大きい。またこれらの効果とともに、 
vo3の場合は低い焼成温度で誘電体磁器組成物を製造
することができ、またYOV2  の場合は共撮周波数
の温度係数τfを小さくすることができる効果がある。
In the present invention, ■oSA, W03 and Y03A
In common, they have the effect of greatly improving the no-load Q, and also have a large dielectric constant. In addition to these effects,
In the case of VO3, a dielectric ceramic composition can be manufactured at a low firing temperature, and in the case of YOV2, there is an effect that the temperature coefficient τf of the co-photography frequency can be made small.

VOs、 、WO3およびYOh の含有量が過度に多
くなると特にQが小さくなシ、比誘電率についても小さ
くなるので、これらの含有量は前記組成式においてx 
+ y + z = 1モルに対して0.0003〜0
.03モル、好ましくはo、o o o s〜0.02
モルの範囲に、するのがよい。
If the content of VOs, WO3, and YOh increases excessively, especially when Q is small, the relative permittivity also becomes small, so these contents are
+ y + z = 0.0003 to 0 per mole
.. 03 mol, preferably o, o o o s ~ 0.02
It is best to keep it within the molar range.

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、バナジウム、タングステン。Titanium, neodymium, vanadium, tungsten.

イツトリウム等の炭酸塩、酸化物、硫酸塩等の出発原料
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 mixing starting materials such as carbonates such as yttrium, oxides, sulfates, etc., calcining the mixture, then shaping, firing, and sintering.

例えば、炭酸バリウム、酸化チタン、酸化ネオジウムお
よび酸化バナジウム、酸化タングステン。
For example, barium carbonate, titanium oxide, neodymium and vanadium oxide, tungsten oxide.

酸化イツトリウム等を各所定量ずつ水、アルコール等の
溶媒と共に湿式混合する。続いて、水、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時門前度仮焼
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100〜10
00Kg/ff1)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1300〜1450″Cで
焼成すれば、上記誘電体磁器組成物が得られる。
A predetermined amount of yttrium oxide or the like is wet-mixed with a solvent such as water or alcohol. Subsequently, after removing water, alcohol, etc., the product is crushed and calcined at 900 to 1100° C. for about 5 hours in an oxygen-containing gas atmosphere (for example, air atmosphere). After pulverizing the calcined material thus formed, it is mixed with an organic binder such as polyvinyl alcohol to make it homogeneous, dried, pulverized, and pressure-molded (pressure 100-100
00Kg/ff1). Then, by firing this molded product at 1300 to 1450''C in an oxygen-containing gas atmosphere such as air, 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、マイクロ波IC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 microwave ICs, 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(BaO03)粉末0.15モル、酸化チ
タン粉末(TiO2) 0.70モル、酸化ネオジウム
粉末(Nd203)  0.15モルおよび酸化バナジ
ウム粉末(VOSA) 0.0005 モルをエタノー
ルと共にボールミルに入れ、10時間湿式混合した。こ
の混合物を、ボールミルから取り出して溶媒のエタノー
ルを蒸発させ、らい潰機で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。
[Example 1] 0.15 mol of barium carbonate (BaO03) powder, 0.70 mol of titanium oxide powder (TiO2), 0.15 mol of neodymium oxide powder (Nd203) and 0.0005 mol of vanadium oxide powder (VOSA) were added to ethanol. The mixture was placed in a ball mill and wet mixed for 10 hours. This mixture was taken out from the ball mill, the solvent ethanol was evaporated, and the mixture was ground in a crusher for 1 hour. The crushed material is
After calcination at 950'C under air atmosphere.

再びらい潰機で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15mm01厚さ5.5簡のベレットに成形して空気
雰囲気下に1360°Cで2時間焼成、焼結して本実施
例の誘電体磁器組成物(0,15BaO=0.70Ti
02 ・0.15Nd203 ’ 0.0O05VO5
A)を得た。
The mixture was crushed again using a crusher for 1 hour. This pulverized material was mixed uniformly with an appropriate amount of polyvinyl alcohol solution, formed into a pellet with a diameter of 15 mm and a thickness of 5.5 mm, and was fired and sintered at 1360°C for 2 hours in an air atmosphere. Example dielectric ceramic composition (0.15BaO=0.70Ti
02 ・0.15Nd203' 0.0O05VO5
A) was obtained.

こうして得られた磁器組成物を直径9 m l +厚さ
31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f。(2〜6 GH2)における無負荷
Qおよび比誘電率ε1を求めた。また。
The thus obtained porcelain composition was cut into a size of 9 ml in diameter and 31 in thickness, and then measured by the dielectric resonance method to find the resonance frequency f. The no-load Q and relative dielectric constant ε1 at (2 to 6 GH2) were determined. Also.

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 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の酸化バナジウム粉末の使用量をかえたほかは
、実施例1と同様にして誘電体磁器組成物を製造し、実
施例1と同様に特性を測定した。
Examples 2 to 5 Dielectric ceramic compositions were produced in the same manner as in Example 1, except that the amount of vanadium oxide powder used in Example 1 was changed, and the properties were measured in the same manner as in Example 1.

その結果を第1表に示す。The results are shown in Table 1.

比較例1〜2 実施例1の酸化バナジウム粉末を使用しなかった(比較
例1)および酸化バナジウム粉末の使用量をo、o o
 o sモルから0.04モルにかえた(比較例2)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
、実施例1と同様に特性を測定した。
Comparative Examples 1 to 2 The vanadium oxide powder of Example 1 was not used (Comparative Example 1), and the amount of vanadium oxide powder used was o, o o
A dielectric ceramic composition was produced in the same manner as in Example 1, except that o s mol was changed to 0.04 mol (Comparative Example 2), and the characteristics were measured in the same manner as in Example 1.

その結果を第1表に示す。The results are shown in Table 1.

第    1    表 毫0.15Ba0 ・0.70Ti02 ・0.15N
d203に対するvOI、/2ノ量実施例6〜9および
比較例3〜5 実施例1の出発原料の使用量をかえたほかは。
1st table 0.15Ba0 ・0.70Ti02 ・0.15N
vOI for d203, /2 amount Examples 6 to 9 and Comparative Examples 3 to 5 Example 1 except that the amount of starting material used was changed.

実施例1と同様にして第2表記載の誘電体磁器組成物を
製造し、実施例1と同様に特性を測定した。
The dielectric ceramic compositions listed in Table 2 were produced in the same manner as in Example 1, and their properties were measured in the same manner as in Example 1.

その結果を第2表に示す。The results are shown in Table 2.

第2表 実施例10〜14 実施例1の酸化バナジウム粉末を酸化タングステン粉末
にかえ、また焼成温度をかえて実施例1と同様に第6表
記載の誘電体磁器組成物を製造し。
Table 2 Examples 10 to 14 The dielectric ceramic compositions listed in Table 6 were produced in the same manner as in Example 1 except that the vanadium oxide powder in Example 1 was replaced with tungsten oxide powder and the firing temperature was changed.

実施例1と同様に特性を測定した。Characteristics were measured in the same manner as in Example 1.

その結果を第6表に示す。The results are shown in Table 6.

第     3    表 * 0.15BaO’ 0.70Ti02−0.15N
d203に対するWO3の量実施例15〜19 実施例1の酸化バナジウム粉末を酸化イツトリウム粉末
にかえ、実施例1と同様に第4表記載の誘電体磁器組成
物を製造し、実施例1と同様に特性を測定した。
Table 3 * 0.15BaO' 0.70Ti02-0.15N
Amount of WO3 relative to d203 Examples 15 to 19 The vanadium oxide powder in Example 1 was replaced with yttrium oxide powder, and the dielectric ceramic compositions listed in Table 4 were produced in the same manner as in Example 1. Characteristics were measured.

その結果を第4表に示す。The results are shown in Table 4.

一\へ 第     4    表 !10.15BaO・0.70Ti 02 ・0.15
Nd203に対するY○3/2ノ量〔発明の効果〕 本発明のvo5/21 wo31 YoF’2 等を含
有したBaO・TiO2・Nd2O3系の誘電体磁器組
成物は、特に無負荷Qが大きい。また比誘電率ε1が大
きく、共振周波数の温度係数τfの安定性がよい。
1\To the 4th table! 10.15BaO・0.70Ti 02・0.15
Amount of Y○3/2 relative to Nd203 [Effect of the invention] The BaO/TiO2/Nd2O3-based dielectric ceramic composition containing vo5/21 wo31 YoF'2 or the like of the present invention has a particularly large no-load Q. Further, the dielectric constant ε1 is large, and the stability of the temperature coefficient τf of the resonance frequency is good.

従って本発明の誘電体磁器組成物は誘電体共振器材料と
して好適であシ、特に0.1〜4 GHz帯で使用され
る共振器材料として使用すると小型で高性能の共振器が
得られる。
Therefore, the dielectric ceramic composition of the present invention is suitable as a dielectric resonator material, and in particular, when used as a resonator material used in the 0.1-4 GHz band, a compact and high-performance resonator can be obtained.

Claims (1)

【特許請求の範囲】 組成式 xBaO・yTiO_2・zNd_2O_3・tMe(
式中、MeはVO_5_/_2、WO_3およびYO_
3_/_2よりなる群から選択された1種以上を示し、
x+y+zを1モルとしたときxは0.1〜0.2モル
、yは0.5〜0.8モル、zは0.1〜0.2モルで
、tはx+y+z=1モルに対して0.0003〜0.
03モルである。) で表わされるバナジウム、タングステンおよびイットリ
ウムよりなる群から選択された1種以上の元素、ネオジ
ウム、チタン、バリウム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・tMe(
In the formula, Me is VO_5_/_2, WO_3 and YO_
Indicates one or more types selected from the group consisting of 3_/_2,
When x + y + z is 1 mol, x is 0.1 to 0.2 mol, y is 0.5 to 0.8 mol, z is 0.1 to 0.2 mol, and t is x + y + z = 1 mol. 0.0003~0.
03 mole. ) A dielectric ceramic composition comprising one or more elements selected from the group consisting of vanadium, tungsten and yttrium, neodymium, titanium, barium and oxygen.
JP60222864A 1985-10-08 1985-10-08 Dielectric porcelain composition Expired - Lifetime JPH0712971B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP60222864A JPH0712971B2 (en) 1985-10-08 1985-10-08 Dielectric porcelain composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP60222864A JPH0712971B2 (en) 1985-10-08 1985-10-08 Dielectric porcelain composition

Publications (2)

Publication Number Publication Date
JPS6283364A true JPS6283364A (en) 1987-04-16
JPH0712971B2 JPH0712971B2 (en) 1995-02-15

Family

ID=16789085

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JPH0712971B2 (en)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6379753A (en) * 1986-09-24 1988-04-09 日本特殊陶業株式会社 Dielectric ceramic composition for high frequency
JPH02242517A (en) * 1989-03-15 1990-09-26 Matsushita Electric Ind Co Ltd Dielectric porcelain composition
JPH02242518A (en) * 1989-03-15 1990-09-26 Matsushita Electric Ind Co Ltd Dielectric porcelain composition
JPH02242522A (en) * 1989-03-15 1990-09-26 Matsushita Electric Ind Co Ltd Dielectric porcelain composition
JPH02242520A (en) * 1989-03-15 1990-09-26 Matsushita Electric Ind Co Ltd Dielectric porcelain composition

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS6379753A (en) * 1986-09-24 1988-04-09 日本特殊陶業株式会社 Dielectric ceramic composition for high frequency
JPH06102572B2 (en) * 1986-09-24 1994-12-14 日本特殊陶業株式会社 High frequency dielectric ceramic composition
JPH02242517A (en) * 1989-03-15 1990-09-26 Matsushita Electric Ind Co Ltd Dielectric porcelain composition
JPH02242518A (en) * 1989-03-15 1990-09-26 Matsushita Electric Ind Co Ltd Dielectric porcelain composition
JPH02242522A (en) * 1989-03-15 1990-09-26 Matsushita Electric Ind Co Ltd Dielectric porcelain composition
JPH02242520A (en) * 1989-03-15 1990-09-26 Matsushita Electric Ind Co Ltd Dielectric porcelain composition

Also Published As

Publication number Publication date
JPH0712971B2 (en) 1995-02-15

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