JPH03216911A - dielectric porcelain composition - Google Patents
dielectric porcelain compositionInfo
- Publication number
- JPH03216911A JPH03216911A JP2011334A JP1133490A JPH03216911A JP H03216911 A JPH03216911 A JP H03216911A JP 2011334 A JP2011334 A JP 2011334A JP 1133490 A JP1133490 A JP 1133490A JP H03216911 A JPH03216911 A JP H03216911A
- Authority
- JP
- Japan
- Prior art keywords
- dielectric
- capacitance
- temperature coefficient
- dielectric constant
- dielectric porcelain
- 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.)
- Pending
Links
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Inorganic Insulating Materials (AREA)
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) [Abstract] 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
本発明は誘電率、絶縁抵抗、絶縁破壊電圧が高く、良好
度Qにすぐれ、静電容量温度係数が小さい誘電体磁器組
成物に関するものである.従来の技術
従来から、誘電率、絶縁抵抗が高く、良好度Qにすぐれ
、静電容量温度係数が小さい誘電体磁器組成物として下
記のような系が知られている.・BaO TiOz
NdzOs系・BaO Tilt Sa
ges系発明が解決しようとする課題
しかし、これらの組成は、例えば0.09BaO −0
.56TiOz 0.35NdOszgの組成比か
らなる誘電体材料を使用し、円板形磁器コンデンサを作
製すると、誘電率:67、静電容量温度係数: N40
GIPII /゜C、良好度Q : 3000、絶縁抵
抗: 8.OX10”Ω、絶縁破壊強度=30κV/
閣であり、満足のできる値ではない.
課題を解決するための手段
これらの課題を解決するために本発明は、一般x[(B
aO) 11−a) (MgO) al yTi
ot lReo3yxと表した時(ただし、x+y+
z=1.00、0<m≦0.50、ReLtLa, P
r+ Nd, Ssから選ばれる一種以上の希土類元素
.)、x,y,zが以下に表す各点a,b,c,d,e
,fで囲まれるモル比の範囲からなることを特徴とする
誘電体磁器組成物を提案するものである.
作用
第1図は本発明にかかる組成物の主成分の組成範囲を示
す三元図であり、主成分の組成範囲を限定した理由を第
1図を参照しながら説明する.すなわち、AfII域で
は焼結が著しく困難である.また、BsJl域では良好
度Qが低下し実用的でな《なる。さらに、C,DiJf
域では静電容量温度係数がマイナス側に大きくなりすぎ
て実用的でなくなる.そして、EfiI域では静電容量
温度係数がプラス方向に移行するが、誘電率が小さく実
用的でなくなる.また、ReをLa, Pr. Nd+
Swから選ぶことにより、La, Pr, Nd,
S一の順で誘電率を大きく下げることなく、静電容量温
度係数をプラス方向に移行することが可能であり、La
, Pr, Nd+ SIlの1種あるいはそれらの組
合せにより静電容量温度係数の調節が可能である.
また、BaOをMgOで置換することにより、誘電率、
良好度Q、絶縁破壊強度の値を大きく変えることなく、
静電容量温度係数をプラス方向に移行させ、絶縁抵抗を
高くする効果を有しているが、その置換率mが0.01
未満では置換効果はなく、方0.50を趨えると誘電率
が低下し実用的でなくなる.
実施例
以下に、本発明を具体的実施例により説明する.(実施
例l)
出発原料には化学的に高純度のBaCOコ, MgO
,TIOI, LatOs+ PrJ+++ NdxO
sおよびSag(h粉末を下記の第1表に示す組成比に
なるように秤量し、めのうボールを備えたゴム内張りの
ボールミルに純水とともに入れ、湿式混合後、脱水乾燥
した.この乾燥粉末を高アルミナ賞のルツボに入れ、空
気中で1100℃にて2時間仮焼した.この仮焼粉末を
、めのうボールを備えたゴム内張りのボールミルに純水
とともに入れ、湿式粉砕後、脱水乾燥した.この粉砕粉
末に、有機バインダーを加え、均質とした後、32メッ
シュのふるいを通して整粒し、金型と油圧プレスを用い
て成形圧力1ton/cjで直径15■、厚み0.4閣
に成形した.次いで、この成形円板をジルコニア粉末を
敷いたアルミナ賞のサヤに入れ、空気中にて下記の第1
表に示す温度で2時間焼成し、第1表に示す組成比の誘
電体磁器を得た.
このようにして得られた誘電体磁器円板は、厚みと直径
を測定し、誘電率、良好度Q、静電容量温度係数測定用
試料は、誘電体磁器円板の両面全体に銀電極を焼き付け
、絶縁抵抗、絶縁破壊強度測定用試料は、誘電体磁器円
板の外周より内側に1閣の幅で銀電極のない部分を設け
、銀電極を焼き付けた.そして、誘電率、良好度Q、静
電容量温度係数は、横河・ヒューレソト・バッカード■
製デジタルLCRメータのモデル4275 Aを使用し
、測定温度20゜C、測定電圧1.OVrms,測定周
波数lMHzでの測定より求めた.なお、静電容量温度
係数は、20゜Cと85゜Cの静電容量を測定し、次式
により求めた.
TC= (C−Co)/CoXi/65XlO”TC:
静電容量温度係数(ppm/”C)Co:20゜Cでの
静電容量( pF )C:85゜Cでの静電容量(pF
)
また、誘電率は次式より求めた.
K= 143.8x C o X t / D”K :
誘電率
Co:20’Cでの静電容量(pP)
D :誘電体磁器の直径 (1)
L :誘電体磁器の厚み (謹)
さらに、絶縁抵抗は、横河・ヒューレット・パッカード
■製HRメータのモデル4329Aを使用し、測定電圧
50V.[l.C.、測定時間1分間による測定より求
めた.
そして、絶縁破壊強度は、菊水電子工業■製高電圧電源
PH535K−3形を使用し、試料をシリコンオイル中
に入れ、昇圧速度5QV/seeにより求めた絶縁破壊
電圧を誘電体厚みで除算し、1一当りの絶縁破壊強度と
した.
試験条件を第1表に併せて示し、試験結果を下記の第2
表に示す.
以下余白
なお、実施例における誘電体磁器の作製方法では、Ba
CO1+ MgO, TiOg+ LaxOs+ Pr
*0+++ Nd,o,およびSexesを使用したが
、この方法に限定されるものではなく、所望の組成比に
なるように、Ba↑10,などの化合物、あるいは炭酸
塩、水酸化物など空気中での加熱により、Bad, M
gO+ riot, LagOs+Pr.O+++
NToOsおよびSm.01となる化合物を使用しても
実施例と同程度の特性を得ることができる.また、上述
の基本組成のほかに、SiOgn MnOg,’eto
3+ ZnOなど一般にフランクスと考えられている塩
類、酸化物などを、特性を損なわない範囲で加えること
もできる.
発明の効果
以上のように本発明によれば、誘電率、絶縁抵抗、絶縁
破壊電圧が高く、良好度Qにすぐれ、静電容量温度係数
が小さいため、製品の小型化、大容量化、特性向上が可
能である.DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a dielectric ceramic composition that has high dielectric constant, high insulation resistance, high dielectric breakdown voltage, excellent Q quality, and low temperature coefficient of capacitance. BACKGROUND OF THE INVENTION Conventionally, the following systems have been known as dielectric ceramic compositions that have a high dielectric constant and insulation resistance, an excellent Q quality, and a small temperature coefficient of capacitance.・BaO TiOz
NdzOs type/BaO Tilt Sa
However, these compositions, for example, 0.09BaO -0
.. When a disk-shaped ceramic capacitor is manufactured using a dielectric material having a composition ratio of 56TiOz and 0.35NdOszg, the dielectric constant: 67 and the capacitance temperature coefficient: N40.
GIPII /°C, quality Q: 3000, insulation resistance: 8. OX10”Ω, dielectric breakdown strength = 30κV/
The price is not satisfactory. Means for Solving the Problems In order to solve these problems, the present invention provides the general x[(B
aO) 11-a) (MgO) al yTi
When expressed as ot lReo3yx (however, x+y+
z=1.00, 0<m≦0.50, ReLtLa, P
r+ One or more rare earth elements selected from Nd and Ss. ), x, y, z are the following points a, b, c, d, e
, f is proposed. FIG. 1 is a ternary diagram showing the composition range of the main components of the composition according to the present invention, and the reason for limiting the composition range of the main components will be explained with reference to FIG. In other words, sintering is extremely difficult in the AfII region. In addition, in the BsJl range, the quality Q decreases, making it impractical. Furthermore, C, DiJf
In the range, the temperature coefficient of capacitance becomes too large on the negative side, making it impractical. In the EfiI region, the temperature coefficient of capacitance shifts to a positive direction, but the dielectric constant is too small to be practical. Also, Re is La, Pr. Nd+
By selecting from Sw, La, Pr, Nd,
It is possible to shift the capacitance temperature coefficient in the positive direction without significantly lowering the dielectric constant in the order of S1, and La
, Pr, Nd+ SIl, or a combination thereof, the temperature coefficient of capacitance can be adjusted. In addition, by replacing BaO with MgO, the dielectric constant,
without significantly changing the quality Q and dielectric breakdown strength values.
It has the effect of shifting the capacitance temperature coefficient in the positive direction and increasing the insulation resistance, but the substitution rate m is 0.01.
If it is less than 0.50, there will be no substitution effect, and if it exceeds 0.50, the dielectric constant will decrease and become impractical. EXAMPLES The present invention will be explained below using specific examples. (Example 1) Chemically high-purity BaCO, MgO are used as starting materials.
, TIOI, LatOs+ PrJ+++ NdxO
S and Sag (h powders were weighed to have the composition ratio shown in Table 1 below, put into a rubber-lined ball mill equipped with agate balls together with pure water, wet mixed, and then dehydrated and dried. This dry powder was It was placed in a high alumina crucible and calcined in air at 1100°C for 2 hours.The calcined powder was placed in a rubber-lined ball mill with agate balls together with pure water, wet-pulverized, and then dehydrated and dried. An organic binder was added to this pulverized powder to make it homogeneous, and then the powder was sized through a 32 mesh sieve, and molded into a diameter of 15 cm and a thickness of 0.4 mm using a mold and a hydraulic press at a molding pressure of 1 ton/cj. Next, this molded disk was placed in an alumina pod covered with zirconia powder, and the following first step was carried out in the air.
It was fired for 2 hours at the temperature shown in the table to obtain dielectric porcelain having the composition ratio shown in Table 1. The thickness and diameter of the dielectric porcelain disk thus obtained were measured, and the samples for measuring the dielectric constant, goodness Q, and capacitance temperature coefficient were prepared using silver electrodes on both sides of the dielectric porcelain disk. The samples for baking, insulation resistance, and dielectric breakdown strength measurements were made by setting a part with no silver electrode on the inside of the outer periphery of a dielectric porcelain disk and baking the silver electrode. And, the dielectric constant, goodness Q, and capacitance temperature coefficient are Yokogawa/Heuresoto/Baccard■
Using a digital LCR meter model 4275 A made by Manufacturer, the measurement temperature was 20°C and the measurement voltage was 1. OVrms, determined from measurements at a measurement frequency of 1MHz. The capacitance temperature coefficient was determined by measuring capacitance at 20°C and 85°C using the following formula. TC=(C-Co)/CoXi/65XlO”TC:
Capacitance temperature coefficient (ppm/”C) Co: Capacitance at 20°C (pF) C: Capacitance at 85°C (pF
) Also, the dielectric constant was calculated from the following formula. K= 143.8x C o X t / D”K:
Dielectric constant Co: Capacitance at 20'C (pP) D: Diameter of dielectric porcelain (1) L: Thickness of dielectric porcelain Using meter model 4329A, the measurement voltage was 50V. [l. C. , determined from measurements with a measurement time of 1 minute. The dielectric breakdown strength was determined by using a high-voltage power supply PH535K-3 manufactured by Kikusui Electronics Corporation, placing the sample in silicone oil, and dividing the dielectric breakdown voltage determined by the voltage increase rate of 5 QV/see by the dielectric thickness. It was taken as the dielectric breakdown strength per unit. The test conditions are also shown in Table 1, and the test results are shown in Table 2 below.
It is shown in the table. In the following margin, in the method for producing dielectric ceramic in the example, Ba
CO1+ MgO, TiOg+ LaxOs+ Pr
*0+++ Although Nd, o, and Sexes were used, the method is not limited to this method. Compounds such as Ba↑10, or carbonates, hydroxides, etc. in the air are used to obtain the desired composition ratio. Bad, M
gO+riot, LagOs+Pr. O+++
NToOs and Sm. Even if a compound of 01 is used, properties comparable to those of the example can be obtained. In addition to the above-mentioned basic composition, SiOgn MnOg, 'eto
3+ Salts and oxides, such as ZnO, which are generally considered Franks, can also be added to the extent that they do not impair the properties. Effects of the Invention As described above, according to the present invention, the dielectric constant, insulation resistance, and dielectric breakdown voltage are high, the quality Q is excellent, and the temperature coefficient of capacitance is small. Improvement is possible.
第1図は本発明にかかる組成物の主成分の組成範囲を説
明する三元図である.
第
l
図FIG. 1 is a ternary diagram illustrating the composition range of the main components of the composition according to the present invention. Figure l
Claims (1)
−yTiO_2−zReO_3_/_2と表した時(た
だし、x+y+z=1.00,0.01<m≦0.50
、ReはLa,Pr,Nd,Smから選ばれる一種以上
の希土類元素。)、x,y,zが以下に表す各点a,b
,c,d,e,fで囲まれるモル比の範囲からなること
を特徴とする誘電体磁器組成物。[Claims] General formula x [(BaO)_(_1_-_m_)(MgO)_m]
-yTiO_2-zReO_3_/_2 (where x+y+z=1.00, 0.01<m≦0.50
, Re is one or more rare earth elements selected from La, Pr, Nd, and Sm. ), x, y, z are each point a, b represented below
, c, d, e, and f.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011334A JPH03216911A (en) | 1990-01-19 | 1990-01-19 | dielectric porcelain composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2011334A JPH03216911A (en) | 1990-01-19 | 1990-01-19 | dielectric porcelain composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH03216911A true JPH03216911A (en) | 1991-09-24 |
Family
ID=11775137
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011334A Pending JPH03216911A (en) | 1990-01-19 | 1990-01-19 | dielectric porcelain composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH03216911A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6844797B2 (en) | 2002-02-21 | 2005-01-18 | Murata Manufacturing Co., Ltd. | High-frequency dielectric ceramic member, dielectric resonator, dielectric filter, dielectric duplexer, and communication device |
-
1990
- 1990-01-19 JP JP2011334A patent/JPH03216911A/en active Pending
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6844797B2 (en) | 2002-02-21 | 2005-01-18 | Murata Manufacturing Co., Ltd. | High-frequency dielectric ceramic member, dielectric resonator, dielectric filter, dielectric duplexer, and communication device |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| JPH03216911A (en) | dielectric porcelain composition | |
| JP2568567B2 (en) | Dielectric porcelain composition | |
| JPH07211140A (en) | Dielectric porcelain composition | |
| JP2568565B2 (en) | Dielectric porcelain composition | |
| JPH0482103A (en) | dielectric porcelain composition | |
| JP2568566B2 (en) | Dielectric porcelain composition | |
| JP2917455B2 (en) | Dielectric porcelain composition | |
| JPH03219502A (en) | dielectric porcelain composition | |
| JP3024768B2 (en) | Dielectric porcelain composition | |
| JPH02242516A (en) | Dielectric porcelain composition | |
| JPH03214507A (en) | Dielectric porcelain composite | |
| JPH042007A (en) | dielectric porcelain composition | |
| JPH0487107A (en) | Dielectric porcelain composition | |
| JPH0482102A (en) | Dielectric porcelain composite | |
| JPH04167306A (en) | dielectric porcelain composition | |
| JPH0498705A (en) | dielectric porcelain composition | |
| JPH04174907A (en) | Dielectric porcelain composition material | |
| JPH04174908A (en) | dielectric porcelain composition | |
| JPH06283028A (en) | Dielectric ceramic composite | |
| JPS62243208A (en) | Dielectric porcelain compound | |
| JPH04357609A (en) | dielectric porcelain composition | |
| JPH04357613A (en) | Dielectric porcelain composition | |
| JPH04357618A (en) | Dielectric porcelain composition | |
| JPH04357612A (en) | Dielectric porcelain composition | |
| JPH04357617A (en) | dielectric porcelain composition |