JPS58143513A - Laminated ceramic condenser - Google Patents

Laminated ceramic condenser

Info

Publication number
JPS58143513A
JPS58143513A JP57026616A JP2661682A JPS58143513A JP S58143513 A JPS58143513 A JP S58143513A JP 57026616 A JP57026616 A JP 57026616A JP 2661682 A JP2661682 A JP 2661682A JP S58143513 A JPS58143513 A JP S58143513A
Authority
JP
Japan
Prior art keywords
laminated ceramic
ceramic condenser
electrodes
present
metals
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
JP57026616A
Other languages
Japanese (ja)
Other versions
JPH0310214B2 (en
Inventor
康信 米田
大西 郭也
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.)
Nichicon Corp
Original Assignee
Nichicon Capacitor 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 Nichicon Capacitor Ltd filed Critical Nichicon Capacitor Ltd
Priority to JP57026616A priority Critical patent/JPS58143513A/en
Publication of JPS58143513A publication Critical patent/JPS58143513A/en
Publication of JPH0310214B2 publication Critical patent/JPH0310214B2/ja
Granted legal-status Critical Current

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  • Inorganic Insulating Materials (AREA)
  • Compositions Of Oxide Ceramics (AREA)
  • Ceramic Capacitors (AREA)
  • Fixed Capacitors And Capacitor Manufacturing Machines (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】 本発明は卑金属電極をもつ積層セラミックコンデンサに
関するものであゐ。
DETAILED DESCRIPTION OF THE INVENTION The present invention relates to a multilayer ceramic capacitor having base metal electrodes.

近年エレクトロニクスの発展とともに電子部品の小形化
が着しく進んできている。セラミックコンデンサにおい
てもグリーンシートの上に電極を印刷し、電極が端面に
交互に寓出しかつ互いに対向するようにグリーンシート
を重ね合せて積層体とし、仁の積層体を熱圧着して空気
中において1200〜1400tで焼成するなどの方法
で得られtrわゆる積層コンデンサとして小形化指向が
一段と進んできている。しかしながら、積場コンデン管
の電極は誘電体磁器と同時焼成を行う九め、磁器材料と
反応せずかつ1200〜1400℃の高温で酸化しない
金属であることが必要である。これらの条件を温良す金
属として白金、バブジウムあるhは両者の合金が用りら
れてきたが、こnらの金属は極めて高価であ勤、積層コ
ンデンサを広範囲に普及させていく上で大きな障害とな
ってい友。
In recent years, with the development of electronics, the miniaturization of electronic components has progressed steadily. In the case of ceramic capacitors, electrodes are printed on green sheets, and the green sheets are layered to form a laminate so that the electrodes are alternately exposed on the end faces and face each other, and the laminate is bonded under heat and placed in air. The trend towards miniaturization of so-called multilayer capacitors, which are obtained by methods such as firing at 1,200 to 1,400 tons, is progressing. However, since the electrodes of the loading dock condenser tube are fired simultaneously with the dielectric porcelain, they must be made of a metal that does not react with the porcelain material and does not oxidize at high temperatures of 1200 to 1400°C. Platinum, babdium, and an alloy of both have been used as metals that meet these conditions, but these metals are extremely expensive and are a major obstacle to widespread use of multilayer capacitors. Become a friend.

このような高価な電−材料に代るものとして、棒金膓電
極で費価な二マケルなどを使用する方法が提案されてお
勤1これらの電極金属は空気中で焼成すると酸化する九
めに還元性雰囲気で焼成する必#があっ九、しかしなが
ら、従来のチタン酸バリウムを生体とし九騎電体磁器材
料では還元雰囲気中で焼成すると半導体化さ−nlしま
い、絶縁抵抗、誘電体損失などの電気特性が着しく劣化
し、コンデンサとして使用できなくなるという欠点があ
っ九。
As an alternative to such expensive electrical materials, a method has been proposed in which the use of expensive metals such as steel metal electrodes has been proposed.1 These electrode metals oxidize when fired in air. However, when firing in a reducing atmosphere, conventional barium titanate bioelectric porcelain materials become semiconducting, resulting in problems such as insulation resistance, dielectric loss, etc. The disadvantage is that the electrical properties of the capacitor deteriorate severely, making it impossible to use it as a capacitor.

本発明はこのような欠点をなくし、還元雰囲気中で焼成
してもすぐft*電気特性を有す為卑金属電極をもつ積
場セラl−yクコンデンすを搗供する−のである。
The present invention eliminates these drawbacks and provides a ceramic condensate having base metal electrodes, which immediately exhibits ft* electrical properties even when fired in a reducing atmosphere.

以下本発明を実施例によ)説明する。The present invention will be explained below with reference to Examples.

炭酸バリウム、炭酸ストロンチウム、酸化チタン、#1
化ジルコニウム%鐙化マグネVつふ、酸化クロム、鹸化
バナVウム、酸化マンガン、酸化スズなどを第1111
K示す組成となるように配合し、16時間fl、を混合
したのち乾燥した。この混合原料を空気中において10
sO〜1200t:で2時間仮焼し、次いで湿式粉砕を
行なう九のち乾燥し大。
Barium carbonate, strontium carbonate, titanium oxide, #1
Zirconium oxide, chromium oxide, saponified vanadium, manganese oxide, tin oxide, etc. No. 1111
The composition was blended to have a composition shown in K, mixed for 16 hours, and then dried. This mixed raw material was placed in the air for 10
Calcined for 2 hours at sO~1200t, then wet-pulverized, then dried.

この粉末に有機バインダーを加え造粒し10■φ、厚み
018mtK成形し九、このようにして得られ友成形体
にN1電極ペーストを8.0111φのスクリーン径を
用いて0雪の分圧の非常に小さい(1000ppm以下
)中性(例えばN、中)あるいは還元雰囲気(Ng/H
t−10010〜90/10 )中1800〜1400
t”で2時開保持し、自然冷却してIIO鵞以下で投入
ガスを止め焼成体をwXX出出友。
An organic binder was added to this powder, and it was granulated and molded to a thickness of 10 mm and a thickness of 018 mt. Small (1000 ppm or less) neutral (e.g. N, medium) or reducing atmosphere (Ng/H
t-10010~90/10) middle 1800~1400
t", keep it open at 2 o'clock, let it cool naturally, stop the gas input below IIO, and turn the fired body into wXX Idetomo.

このようにして得られ九Ni電極をもっ誘電捧磁器の電
気的特性を1lljl、その結果を11!1表に併せて
示しえ。
Show the electrical characteristics of the dielectric porcelain having nine Ni electrodes obtained in this way, and show the results in Table 11!1.

第1表の静電審量(Cap)、誘電体損失(mJ)はI
Vrms*IKHsでOm、絶縁抵抗(IR)は5゜V
、DC!、 1分間印加後の一定値をそれぞれ示した。
The electrostatic capacity (Cap) and dielectric loss (mJ) in Table 1 are I
Vrms*IKHs is Om, insulation resistance (IR) is 5°V
, DC! , respectively, showed a constant value after application for 1 minute.

′&お、慶中の試料番号KO印を付し良ものは本発明0
IIII外のものであ)、そn以外はすべて零殆明範園
内のものである。本発明によるものは中性1えは還元雰
囲気でOwh成で、すぐnた電気特性が得られることが
わかる。
'& O, Keichu's sample number KO mark is attached and the good one is the present invention 0
(It is outside of III), and all other works are within Reimeihanen. It can be seen that the material according to the present invention can be formed in a neutral or reducing atmosphere, and can immediately obtain superior electrical characteristics.

##1”lO@@$ l ah@@ l Hoe l 
NQ c′!NNN ガ町セ 〜へ寮へへへ〜へ包00
 C5d o ci o o ci(50ci c:;
 ci c5 ci ci::::::::”::::
:::: 本発明にお^て組成範囲を限定し友理由は次の通シであ
る。すなわち、ムヤイト(Ba”イオン)とBサイト(
Ti4’″イオン)の比(A/B)が1.00以下では
還元され、絶縁抵抗が急激に低下する。
##1”lO@@$ l ah@@ l Hoe l
NQ c′! NNN ga town se ~he dormitory hehe~he package 00
C5d o ci o o ci (50ci c:;
ci c5 ci ci::::::::”::::
:::: The reasons for limiting the composition range in the present invention are as follows. That is, Muyite (Ba” ion) and B site (
If the ratio (A/B) of Ti4''' ions is less than 1.00, it will be reduced and the insulation resistance will drop sharply.

Xが0.4を越えると、壕九yは0,3を越えると焼結
しなくなる。さらKMnb Or%Snb Vb Mg
を添加しない場合、およびζnもの金属あるいはその化
合物以外の金属あるいはその化合物を添加した場合は絶
縁抵抗が低下する* Mn s Cr、■、Snでは1
.0wt%を越えると&a麺の融着がおこるだけでなく
絶縁抵抗が低下する。一方Mgでは1.Ow t%を越
えると焼結しなくなるためである。なお、賽施例ではN
1電−ペーストを用い九が、X線マイクロアナライザー
によって断面を分析した結果、N1の磁器への拡散は全
くなく、さらにN1電極ベースト以外の電極としてW%
Moを用いても同様の結果が得られている。
When X exceeds 0.4, trench 9 y does not sinter when it exceeds 0.3. SaraKMnb Or%Snb Vb Mg
Insulation resistance decreases when ζn metals or metals other than their compounds or their compounds are added * 1 for Mn s Cr, ■, and Sn
.. If it exceeds 0 wt%, not only will fusion of &a noodles occur, but also the insulation resistance will decrease. On the other hand, Mg has 1. This is because if the content exceeds Owt%, sintering will not occur. In addition, in the lottery, N
As a result of analyzing the cross section using an X-ray microanalyzer using the 1-electrode paste, it was found that there was no diffusion of N1 into the porcelain, and furthermore, as electrodes other than the N1 electrode base, W%
Similar results have been obtained using Mo.

まえ本発明の麿或でかつ電極としてNil[極ペースト
ヲ用匹11作し九積jI11−ラミプクコンデンサでは
、絶縁抵抗が1011以上、−一が2,0%以下とす、
ぐnえ誘電特性が得られる。
In the case of the Nil paste of the present invention as an electrode, the insulation resistance is 1011 or more and -1 is 2.0% or less.
Even better dielectric properties can be obtained.

以上のように本発明によれば中性オたは還元性雰自気中
で焼成してもすぐれた電気特性を得ることができる。し
友かつ・てニヅケルなどの安iIi&卑金属材料を電W
に用いているので、積春セラミプクコンデンサの製造コ
ストを着しく低減することかで謹、工業上極めて大きな
効果を有するものである。
As described above, according to the present invention, excellent electrical properties can be obtained even when fired in a neutral or reducing atmosphere. Electrically converts cheap and base metal materials such as Shitomo Katsuki and Tenizukeru
Since it is used in the production of ceramic capacitors, it has a significant industrial effect by significantly reducing the manufacturing cost of ceramic capacitors.

Claims (1)

【特許請求の範囲】 一般式(Bad−mart)ム(Ti s−y Zry
)B+iwt%Mにおいて、菫、7% A/B% zs
 Mが次の範囲からなる誘電体磁器に卑金属電極を形成
してなることを特徴とする積増セラミックコンデンサ。 0 < x≦0.4       0≦y≦0.31.
00<A/B≦1.05  0<z≦1,0M−Mls
 Cr%V% M118”%In、 Wtv酸化物
[Claims] General formula (Bad-mart)
) In B+iwt%M, violet, 7% A/B% zs
A multilayer ceramic capacitor characterized in that a base metal electrode is formed on a dielectric ceramic in which M is in the following range. 0<x≦0.4 0≦y≦0.31.
00<A/B≦1.05 0<z≦1,0M-Mls
Cr%V% M118”%In, Wtv oxide
JP57026616A 1982-02-19 1982-02-19 Laminated ceramic condenser Granted JPS58143513A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57026616A JPS58143513A (en) 1982-02-19 1982-02-19 Laminated ceramic condenser

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57026616A JPS58143513A (en) 1982-02-19 1982-02-19 Laminated ceramic condenser

Publications (2)

Publication Number Publication Date
JPS58143513A true JPS58143513A (en) 1983-08-26
JPH0310214B2 JPH0310214B2 (en) 1991-02-13

Family

ID=12198412

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57026616A Granted JPS58143513A (en) 1982-02-19 1982-02-19 Laminated ceramic condenser

Country Status (1)

Country Link
JP (1) JPS58143513A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100415560B1 (en) * 2000-03-31 2004-01-24 삼성전기주식회사 Dielectric ceramic composition, ceramic capacitor using the composition and process of producing same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5324600A (en) * 1976-08-19 1978-03-07 Murata Manufacturing Co Nonnreducing dielectric ceramic composition
JPS5567568A (en) * 1978-11-10 1980-05-21 Murata Manufacturing Co Nonreducible dielectric porcelain composition and preparing ceramic laminated capacitor using same

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5324600A (en) * 1976-08-19 1978-03-07 Murata Manufacturing Co Nonnreducing dielectric ceramic composition
JPS5567568A (en) * 1978-11-10 1980-05-21 Murata Manufacturing Co Nonreducible dielectric porcelain composition and preparing ceramic laminated capacitor using same

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100415560B1 (en) * 2000-03-31 2004-01-24 삼성전기주식회사 Dielectric ceramic composition, ceramic capacitor using the composition and process of producing same

Also Published As

Publication number Publication date
JPH0310214B2 (en) 1991-02-13

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