JPS63121209A - Non-reducing dielectric ceramic composition - Google Patents

Non-reducing dielectric ceramic composition

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Publication number
JPS63121209A
JPS63121209A JP61266406A JP26640686A JPS63121209A JP S63121209 A JPS63121209 A JP S63121209A JP 61266406 A JP61266406 A JP 61266406A JP 26640686 A JP26640686 A JP 26640686A JP S63121209 A JPS63121209 A JP S63121209A
Authority
JP
Japan
Prior art keywords
dielectric ceramic
ceramic composition
parts
weight
main component
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
Application number
JP61266406A
Other languages
Japanese (ja)
Inventor
優 藤野
西岡 吾朗
行雄 坂部
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.)
Murata Manufacturing Co Ltd
Original Assignee
Murata Manufacturing 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 Murata Manufacturing Co Ltd filed Critical Murata Manufacturing Co Ltd
Priority to JP61266406A priority Critical patent/JPS63121209A/en
Publication of JPS63121209A publication Critical patent/JPS63121209A/en
Pending legal-status Critical Current

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  • 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) [Summary] This bulletin contains application data before electronic filing, so abstract data is not recorded.

Description

【発明の詳細な説明】 く産業上の利用分野〉 この発明は酸素分圧の低い非酸化性雰囲気中で、かつ1
360℃以下の温度で焼結し、温度に対する静電容量の
変化率が小さく、誘電率が200以上、誘電体損失が0
.2%以下であり、20℃における比抵抗が1×101
2Ωaより大きいことを特徴とする非還元性誘電体磁器
組成物に関するものである。
[Detailed description of the invention] Industrial application field> The present invention is directed to a non-oxidizing atmosphere with a low oxygen partial pressure, and
Sintered at a temperature of 360℃ or less, the rate of change in capacitance with respect to temperature is small, the dielectric constant is 200 or more, and the dielectric loss is 0.
.. 2% or less, and the specific resistance at 20°C is 1 x 101
The present invention relates to a non-reducible dielectric ceramic composition characterized in that the resistance is larger than 2Ωa.

〈従来の技術およびその問題点〉 従来、チタン酸バリウムを主体とした誘電体材料を用い
ることにより、小型で大容量、かつ高信頼性のセラミッ
クス積層コンデンサが得られておリ、電子計算機、通信
握、テレビ受像握、電子時計、ラジオ受信機など各種製
品の電子回路に使用されている。
<Conventional technology and its problems> Conventionally, small, large-capacity, and highly reliable ceramic multilayer capacitors have been obtained by using dielectric materials mainly made of barium titanate. It is used in the electronic circuits of various products such as grips, TV receivers, electronic clocks, and radio receivers.

しかし、これらのチタン酸バリウムを主体とする組成系
は自然雰囲気中1300〜1400℃で焼成することが
必要であるため、内部電極には白金、パラジウムなどの
貴金属を使用しなければならないという欠点を有してい
た。
However, these composition systems mainly composed of barium titanate require firing at 1,300 to 1,400°C in a natural atmosphere, so they have the disadvantage of requiring the use of noble metals such as platinum and palladium for the internal electrodes. had.

即ち、内部電極の材料としては、 (1)誘電体が焼結する温度で溶融したり、蒸発したり
しないこと。
That is, the material for the internal electrodes should: (1) not melt or evaporate at the temperature at which the dielectric is sintered;

(2)焼成雰囲気によって酸化したり、誘電体と接触し
て反応を起こさないこと。
(2) It should not be oxidized by the firing atmosphere or react by coming into contact with the dielectric.

などの条件を満足する必要があった。It was necessary to satisfy the following conditions.

従って、セラミックス$A層コンデンサのコストを低下
させるためには、内部電極を負金属から卑金属にする必
要があるが、卑金属の例えばニッケルを内部電極材料と
して用いるためには、酸素分圧の低い非酸化性雰囲気中
で1360℃以下の焼成温度で焼結可能な誘電体磁器が
必要であった。
Therefore, in order to reduce the cost of ceramic $A-layer capacitors, it is necessary to change the internal electrodes from negative metals to base metals. However, in order to use base metals such as nickel as the internal electrode material, it is necessary to use non-negative metals with low oxygen partial pressure. There was a need for dielectric porcelain that could be sintered at a firing temperature of 1360° C. or lower in an oxidizing atmosphere.

く問題点を解決するための手段〉 この発明は上記した問題点を解潤するためになされたも
のであって、その要旨とするところは(Sr1−x C
a x) 、1(T、1−y Mg、 ) Osで表わ
される組成式において、上式のx、y、mがモル比率で
0.3≦x≦0.5.0.001≦y≦0.020.0
.98≦m≦ 1.02の範囲を満足し、かつ上記主成
分を1001ffi部としたとき、副成分として1を1
1n Otに換算して0.01〜2.00重量部、ある
いはさらにSL Otを3.00重置部以下含有するこ
とを特徴とする非還元性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。
Means for Solving the Problems> This invention has been made to solve the above problems, and its gist is (Sr1-x C
In the compositional formula represented by a 0.020.0
.. When the range of 98≦m≦1.02 is satisfied and the above main component is 1001ffi parts, 1 is 1 as a subcomponent.
The purpose of the present invention is to provide a non-reducible dielectric ceramic composition characterized by containing 0.01 to 2.00 parts by weight of SL Ot in terms of 1n Ot, or 3.00 parts by weight or less of SL Ot. It is something to do.

〈作用〉 この発明の組成式(Sr1−x Cax ) m (r
、1−yM;+、)03で表わされる誘電体磁器組成物
において、上式の係数x1yおよびmをモル比率にて0
.3≦x≦0.5.0.001≦y≦0.020.0.
98≦m≦1.02と限定する理由についてべる。
<Operation> The compositional formula (Sr1-x Cax ) m (r
, 1-yM;+, )03, the coefficients x1y and m in the above formula are 0 in molar ratio.
.. 3≦x≦0.5.0.001≦y≦0.020.0.
Let's talk about the reason for limiting 98≦m≦1.02.

係数Xが0.3より小さいと焼成温度が1360℃を越
え、また温度に対する静電容Ωの変化率が太きくなり好
ましくない。また0、5より大きいと温度に対する静電
容量の変化率が大きくなるため好ましくない。
If the coefficient X is smaller than 0.3, the firing temperature will exceed 1360° C., and the rate of change in capacitance Ω with respect to temperature will become large, which is not preferable. Moreover, if it is larger than 0.5, the rate of change of capacitance with respect to temperature becomes large, which is not preferable.

係数yをo、ooi≦y≦0.020の範囲とするのは
、o、ooiより小さいときは焼成温度が1360℃よ
り高くなって好ましくなく、また0、020より大きい
ときは、誘電体損失(tanδ)が0.2%より大きく
なり、かつ比抵抗が1×1012Ω国より低くなって好
ましくないためである。
Setting the coefficient y in the range o, ooi≦y≦0.020 is undesirable because if it is smaller than o, ooi, the firing temperature will be higher than 1360°C, and if it is larger than 0,020, it will cause dielectric loss. This is because (tan δ) becomes larger than 0.2% and the specific resistance becomes lower than 1×10 12 Ω, which is not preferable.

また、係数mについては、その値が0.98より小さい
ときは、焼成温度が1360°Cを越え、tanδが0
.2%より大きくなり、かつ比抵抗が1×1012Ωα
より低くなって好ましくなく、またmが1.02より大
きいときは誘電率が200より小さく、tanδが0.
2%より大きくなり、比抵抗が1×1012Ωaより低
くなって好ましくない。
Regarding the coefficient m, when the value is smaller than 0.98, the firing temperature exceeds 1360°C and tan δ is 0.
.. 2% and the specific resistance is 1×1012Ωα
When m is larger than 1.02, the dielectric constant is smaller than 200 and tan δ is 0.
If it becomes larger than 2%, the specific resistance becomes lower than 1×10 12 Ωa, which is not preferable.

次に副成分添加量の範囲限定理由についてのべると、主
成分を100重Q部としたとき、−虫の添加量が0.0
1重塁部より少ないと、焼成温度が1360℃を越え、
かつtanδが0.2%より大きくなり、比抵抗も1×
1012Ωσより低くなり好ましくない。また200重
争部上り多いときは、焼成温度が1360℃を越え、か
つtanδが0.2%より大きくなって好ましくない。
Next, we will talk about the reason for limiting the range of the added amount of subcomponents. When the main component is 100 parts by weight, the added amount of insects is 0.0
If it is less than 1 layered part, the firing temperature will exceed 1360℃,
And tan δ is larger than 0.2%, and the specific resistance is also 1×
It becomes lower than 1012Ωσ, which is not preferable. Moreover, when the number of 200 overlap portions increases, the firing temperature exceeds 1360° C. and the tan δ becomes larger than 0.2%, which is not preferable.

SL Orの添加は焼成温度の定価を目的とするもので
あるが、その添加Oが3.00 重ffi部より多くな
ると、tanδが0.2%より大きくなり、かつ比抵抗
が1×1012Ωαより低くなるため好ましくない。
The purpose of adding SL Or is to adjust the firing temperature, but if the added O exceeds 3.00 parts ffi, tan δ will become larger than 0.2% and the specific resistance will become lower than 1 × 10 12 Ωα. This is not desirable because it becomes low.

〈実施例〉 以下、この発明を実施例により詳細に説明する。<Example> Hereinafter, this invention will be explained in detail with reference to Examples.

出発原料として工業用のSr Co 3 、Ca Co
 s 、 I’b Co s、Ti(h、r’ho7、
SL Otを用いて組成式(Sr 1−x Ca 8)
、。
Industrial Sr Co 3 , Ca Co as starting materials
s, I'b Co s, Ti(h, r'ho7,
Compositional formula (Sr 1-x Ca 8) using SL Ot
,.

<T   1%  ) Os+t’hOt+5LOtニ
j5イテ、夫々第しi−y    y 1表に示す配合比になるように配合した。
<T1%)Os+t'hOt+5LOtNij5ite, respectively, were blended so that the blending ratios shown in Table 1 were obtained.

次に、これら配合原料をボールミルにて湿式混合し、粉
砕したのち、蒸発乾燥させ、1150℃で2時間自然雰
囲気中で仮焼した。次いで仮焼した原料に結合材として
酢酸ビニル系バインダーを5重量部加え、ボールミルに
よって湿式混合し、さらに蒸発乾燥、整粒の工程を経て
、得られた粉末原料を2.5ton 4の圧力にて直径
10顯、厚さ 1.2闇の円板状に成形した。
Next, these raw materials were wet mixed in a ball mill, pulverized, evaporated to dryness, and calcined at 1150° C. for 2 hours in a natural atmosphere. Next, 5 parts by weight of a vinyl acetate binder as a binder was added to the calcined raw material, wet mixed using a ball mill, and then subjected to evaporation drying and sizing processes, and the resulting powder raw material was heated at a pressure of 2.5 tons 4. It was molded into a disk shape with a diameter of 10 mm and a thickness of 1.2 mm.

次にこの円板をジルコニア粉末を敷粉としたアルミナ買
置に入れ、自然雰囲気中500℃、2時間で11ビニル
系バインダーを燃焼させたのち、体積比率で82 / 
Na −3/100の還元ガス雰囲気中において、12
70〜1360℃で2時間焼成した。
Next, this disk was placed in an alumina container with zirconia powder as a powder, and after burning the 11 vinyl binder at 500℃ in a natural atmosphere for 2 hours, the volume ratio was 82 /
In a reducing gas atmosphere of Na-3/100, 12
It was baked at 70 to 1360°C for 2 hours.

焼結した素子の両面に民−軛合金を塗布し、誘電率(ε
)および誘電体損失(tanδ)を1KHz。
A min-yoke alloy is applied to both sides of the sintered element, and the dielectric constant (ε
) and dielectric loss (tanδ) at 1KHz.

1 Vris 、 20℃の条件で測定した。Measured under the conditions of 1 Vris and 20°C.

なお温度に対する静電容母変化率は20℃の静電容量値
を基準として一25℃と85℃で測定した。
Note that the capacitance change rate with respect to temperature was measured at -25°C and 85°C with the capacitance value at 20°C as a reference.

また比抵抗(ρ)は20℃において500■の直流電圧
を印加した時に流れる電流値より求めた。その結果は第
2表に示した。なお試料番号に*印のあるものはこの発
明の請求範囲外のものである。
Further, the specific resistance (ρ) was determined from the value of the current flowing when a DC voltage of 500 μm was applied at 20°C. The results are shown in Table 2. Note that sample numbers marked with * are outside the scope of the claims of this invention.

第    1    表 第   2   表 く発明の効果〉 上表から、この発明の組成物においては、焼成温度が1
360℃以下であり、温度に対する静電容nの変化率が
小さく、誘電率が200以上、誘電体損失が0.2%以
下であり、20℃における比抵抗が1×1012Ωa以
上のものが得られることが認められた。
Table 1 Table 2 Effects of the invention> From the above table, it can be seen that in the composition of this invention, the firing temperature is 1.
360°C or less, the rate of change in capacitance n with respect to temperature is small, the dielectric constant is 200 or more, the dielectric loss is 0.2% or less, and the specific resistance at 20°C is 1 x 1012 Ωa or more. This was recognized.

なお、実施例において焼成雰囲気はN、 −82からな
る非酸化性雰囲気を用いたが、Ar、CO,CO2、N
2、N2およびこれらの混合雰囲気ガスを用いてもよい
In the examples, a non-oxidizing atmosphere consisting of N, -82 was used as the firing atmosphere, but Ar, CO, CO2, N
2, N2, and a mixed atmosphere gas thereof may be used.

Claims (1)

【特許請求の範囲】 (1)組成式(Sr_1_−_xCa_x)_m(Ti
_1_−_yMg_y)O_3で表わされる物質を主成
分とする誘電体磁器組成物において、上式のx、yおよ
びmが夫々モル比率にて 0.3≦x≦0.5 0.001≦y≦0.020 0.98≦m≦1.02 の範囲にあり、かつ主成分を100重量部としたとき副
成分としてMnをMnO_2に換算して0.01〜2.
00重量部含有することを特徴とする非還元性誘電体磁
器組成物。 (2)組成式(Sr_1_−_xCa_x)_m(Ti
_1_−_yMg_y)O_3で表わされる物質を主成
分とする誘電体磁器組成物において、上式のx、yおよ
びmが夫々モル比率にて 0.3≦x≦0.5 0.001≦y≦0.020 0.98≦m≦1.02 の範囲にあり、かつ主成分を100重量部としたとき副
成分としてMnをMnO_2に換算して0.01〜2.
00重量部、さらにSiO_2を3.00重量部以下含
有することを特徴とする特許請求の範囲第1項記載の非
還元性誘電体磁器組成物。
[Claims] (1) Composition formula (Sr_1_-_xCa_x)_m(Ti
In a dielectric ceramic composition whose main component is a substance represented by _1_-_yMg_y)O_3, x, y, and m in the above formula each have a molar ratio of 0.3≦x≦0.5 0.001≦y≦ 0.020 0.98≦m≦1.02, and when the main component is 100 parts by weight, Mn as a subcomponent is 0.01 to 2.
A non-reducible dielectric ceramic composition characterized by containing 0.00 parts by weight. (2) Compositional formula (Sr_1_-_xCa_x)_m(Ti
In a dielectric ceramic composition whose main component is a substance represented by _1_-_yMg_y)O_3, x, y, and m in the above formula each have a molar ratio of 0.3≦x≦0.5 0.001≦y≦ 0.020 0.98≦m≦1.02, and when the main component is 100 parts by weight, Mn as a subcomponent is 0.01 to 2.
2. The non-reducible dielectric ceramic composition according to claim 1, further comprising 3.00 parts by weight of SiO_2.
JP61266406A 1986-11-08 1986-11-08 Non-reducing dielectric ceramic composition Pending JPS63121209A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP61266406A JPS63121209A (en) 1986-11-08 1986-11-08 Non-reducing dielectric ceramic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP61266406A JPS63121209A (en) 1986-11-08 1986-11-08 Non-reducing dielectric ceramic composition

Publications (1)

Publication Number Publication Date
JPS63121209A true JPS63121209A (en) 1988-05-25

Family

ID=17430487

Family Applications (1)

Application Number Title Priority Date Filing Date
JP61266406A Pending JPS63121209A (en) 1986-11-08 1986-11-08 Non-reducing dielectric ceramic composition

Country Status (1)

Country Link
JP (1) JPS63121209A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003087012A1 (en) * 2002-04-16 2003-10-23 Murata Manufacturing Co., Ltd. Nonreducing dielectric ceramic, its production method, and multilayer ceramic capacitor

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003087012A1 (en) * 2002-04-16 2003-10-23 Murata Manufacturing Co., Ltd. Nonreducing dielectric ceramic, its production method, and multilayer ceramic capacitor
US7498285B2 (en) 2002-04-16 2009-03-03 Murata Manufacturing Co., Ltd. Nonreducing dielectric ceramic, and manufacturing method and monolithic ceramic capacitor of the same

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