JPS63166105A - Dielectric ceramic composition - Google Patents

Dielectric ceramic composition

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Publication number
JPS63166105A
JPS63166105A JP31224786A JP31224786A JPS63166105A JP S63166105 A JPS63166105 A JP S63166105A JP 31224786 A JP31224786 A JP 31224786A JP 31224786 A JP31224786 A JP 31224786A JP S63166105 A JPS63166105 A JP S63166105A
Authority
JP
Japan
Prior art keywords
temperature
ceramic composition
dielectric ceramic
materials
dielectric constant
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
JP31224786A
Other languages
Japanese (ja)
Inventor
純一 加藤
横谷 洋一郎
博司 加賀田
洋 丹羽
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.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial 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 Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Priority to JP31224786A priority Critical patent/JPS63166105A/en
Publication of JPS63166105A publication Critical patent/JPS63166105A/en
Pending 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1150℃以下の温度で焼成が可能な温度補償
用誘電体磁器組成物に関する。
DETAILED DESCRIPTION OF THE INVENTION Field of Industrial Application The present invention relates to a temperature-compensating dielectric ceramic composition that can be fired at a temperature of 1150° C. or lower.

従来の技術 セラミックコンデンサに用いる温度補償用材料としては
、MgO−CaO−TiO2系の材料(例えば、特開昭
48−86097号公報など)や、La203−TiO
2系の材料(例えば、特開昭51−30400号公報な
ど)が用いられてきたが、これらのオオ料は焼成温度が
1250〜1400℃と高温であるため、積層セラミッ
クコンデンサに用いるときには、内部電極として高価な
白金やパラジウムの電極が必要である。
Conventional technology Temperature compensation materials used in ceramic capacitors include MgO-CaO-TiO2-based materials (for example, Japanese Patent Application Laid-Open No. 48-86097), La203-TiO2, etc.
2-based materials (for example, Japanese Patent Application Laid-Open No. 51-30400) have been used, but since the firing temperature of these materials is as high as 1250 to 1400°C, when used in multilayer ceramic capacitors, internal Expensive platinum or palladium electrodes are required.

一方、高誘電率系の材料では、近年PbOを主体とする
複合ペロブスカイト系の材料が、1000℃前後の低い
焼成温度と優れた誘電体特性を示すことが見いだされ、
電極としてより安価な銀糸の電極が使用出来るため、数
多(の組成物が提案されている。例えば、特開昭60−
21857号公報に開示されているPbTi0 a −
Pb(Mgxz2W1,2)03系では、焼成温度が1
000℃近傍で、高誘電率系の材料である。
On the other hand, among high dielectric constant materials, it has recently been discovered that composite perovskite materials mainly composed of PbO exhibit low firing temperatures of around 1000°C and excellent dielectric properties.
Since cheaper silver thread electrodes can be used as electrodes, many compositions have been proposed.
PbTi0 a − disclosed in Publication No. 21857
In the Pb(Mgxz2W1,2)03 system, the firing temperature is 1
It is a material with a high dielectric constant at around 000°C.

発明が解決しようとする問題点 従来用いられてきた温度補償用セラミックコンデンサ材
料は焼成温度が高いため高価な電極を必要とするが、よ
り安価な銀糸の電極を使用するため1150℃以下の温
度で焼成が可能な誘電体が切望されている。PbOを主
体とする複合ペロブスカイト系の材料では誘電率の温度
変化が大きく、温度補償用のコンデンサに使用できる材
料は知られていない。
Problems to be Solved by the Invention Conventionally used temperature-compensating ceramic capacitor materials require expensive electrodes due to the high firing temperature. There is a strong need for dielectric materials that can be fired. Composite perovskite materials mainly composed of PbO have a large temperature change in dielectric constant, and there are no known materials that can be used in temperature compensation capacitors.

本発明は、かかる現状に鑑み低い焼成温度と小さな温度
変化率を有する誘電体磁器組成物を提供することを目的
とする。
In view of the current situation, an object of the present invention is to provide a dielectric ceramic composition having a low firing temperature and a small rate of temperature change.

問題点を解決するための手段 PbTi、、(Mg宣t2W1za )yOC1で表さ
れる固溶体のPbを、一部Caで置換する。
Means for Solving the Problem Part of Pb in the solid solution represented by PbTi, (Mgxt2W1za)yOC1 is replaced with Ca.

作用 P’bTil−V(Mgt、2Wl/11 )、 OC
1のPbを一部Caで置換することにより、低温焼結性
を損なわず、温度補償用の特性を得ることができる。
Action P'bTil-V (Mgt, 2Wl/11), OC
By partially replacing Pb in No. 1 with Ca, characteristics for temperature compensation can be obtained without impairing low-temperature sinterability.

実施例 出発原料として、化学的に高純度なPbO,CaCo3
 、TiO2,MgO,WO3を用いた。これらを純度
補正をおこなったうえで所定量を秤量し、メノウ製玉石
を用い純水を溶媒としてボールミルで17時時間式混合
した。これを吸引ろ過して水分の大半を分離した後乾燥
し、その後ライカイ機で充分解砕した後、粉体量の5w
t%の水分を茄え、成形圧力500 kg / cdで
、直径60m、高さ約50mの円柱状に成形した。これ
をアルミナルツボ中に入れ同質のフタをし、750℃〜
880℃で2時間仮焼した。次に仮焼物をアルミナ乳鉢
で粗砕し、さらにメノウ製玉石を用い純水を溶媒として
ボールミルで17時間粉砕し、これを吸引ろ過し水分の
大半を分離した後乾燥した。以上の仮焼、粉砕、乾燥を
数回(りかえした後この粉末にポリビニルアルコール6
wt%水溶液を粉体量の6wt%加え、32メツシユふ
るいを通して造粒し、成形圧力1000に+r/cjで
、直径13m、高さ約5Mの円柱状に成形した。成形物
を空気中で700℃まで昇温し1時間保持することによ
り、ポリビニルアルコール分をバーンアウトし、冷却後
これをマグネシャ磁器容器に移し、同質のフタをし、空
気中で所定温度まで400℃/hrで昇温し2時間保持
後400℃/hrで降温した。
Examples As starting materials, chemically high purity PbO, CaCo3
, TiO2, MgO, and WO3 were used. After correcting the purity of these, a predetermined amount was weighed and mixed in a ball mill for 17 hours using agate cobblestones and pure water as a solvent. This is suction filtered to remove most of the moisture, dried, and then thoroughly crushed using a Raikai machine.
It was soaked in t% moisture and molded into a cylinder with a diameter of 60 m and a height of about 50 m at a molding pressure of 500 kg/cd. Place this in an aluminum crucible, cover with the same quality lid, and heat to 750℃~
It was calcined at 880°C for 2 hours. Next, the calcined product was roughly crushed in an alumina mortar, and further crushed in a ball mill using agate cobblestones and pure water as a solvent for 17 hours, filtered with suction to remove most of the moisture, and then dried. After repeating the above steps of calcination, crushing, and drying several times, this powder was mixed with polyvinyl alcohol 6
A wt% aqueous solution was added at 6 wt% of the powder amount, and the mixture was granulated through a 32-mesh sieve, and molded into a cylindrical shape with a diameter of 13 m and a height of about 5 m at a molding pressure of 1000 +r/cj. The molded product was heated to 700°C in the air and held for 1 hour to burn out the polyvinyl alcohol, and after cooling, it was transferred to a Magnesia porcelain container, covered with a similar lid, and heated to a specified temperature in the air for 400°C. The temperature was raised at a rate of 400° C./hr, held for 2 hours, and then lowered at a rate of 400° C./hr.

焼成物は厚さllll11の円板状に切断し、両面にC
r−Auを蒸着し誘電率、QをI MHz、 I V/
msの電界下で測定した。また抵抗率は20℃で1kV
/1llIの電圧を印加後1分値から求めた。
The fired product was cut into a disk shape with a thickness of lllll11, and both sides were coated with C.
r-Au was evaporated and the dielectric constant and Q were set to I MHz, IV/
Measurements were made under an electric field of ms. Also, the resistivity is 1kV at 20℃
The voltage of /1llI was determined from the value 1 minute after application.

なお焼成温度は焼成物の密度がもつとも太き(なる温度
とした。
The firing temperature was determined to be the temperature at which the density of the fired product was as high as possible.

第1表に本発明の組成範囲および周辺組成の成分、焼成
温度、誘電率、Q%誘電率の温度変化率、抵抗率を示す
Table 1 shows the composition range of the present invention, peripheral composition components, firing temperature, dielectric constant, temperature change rate of Q% dielectric constant, and resistivity.

(以下余白) 第1表 本印は発明の範囲外の比較例 発明の範囲外の組成物は、表1のNo、に*印をつけた
試料を例として挙げたが、catが0.6を越えると最
適焼成温度が1150℃を越え、0゜4以下では誘電率
の変化率が3000ppm/’C以上となる、あるいは
Ti量が0.6以下ではQが1000以下となる等の難
点を有している。
(Leaving space below) Table 1: Comparative examples outside the scope of the invention Compositions outside the scope of the invention are samples marked with an asterisk (*) in No. of Table 1, and the cat is 0.6. If the temperature exceeds 1,150℃, the optimum firing temperature will exceed 1150℃, if the temperature is 0℃ or less, the rate of change in dielectric constant will be 3000ppm/'C or more, or if the Ti amount is 0.6 or less, Q will be 1000 or less. have.

発明の効果 本発明の誘電体磁器組成物によれば、誘電率の温度変化
率が3000ppm/℃以下、Qが1000以上の特性
が得られ、さらに1150℃以下の温度で焼成できるの
で、積層コンデンサ素子の内部電極としてAg−Pd系
の材料を用いることが可能であり、安価な積層コンデン
サを実現できるので工業的価値が大である。
Effects of the Invention According to the dielectric ceramic composition of the present invention, characteristics such as a temperature change rate of dielectric constant of 3000 ppm/°C or less and a Q of 1000 or more can be obtained, and furthermore, since it can be fired at a temperature of 1150°C or less, it can be used for multilayer capacitors. It is possible to use Ag-Pd-based materials as the internal electrodes of the element, and an inexpensive multilayer capacitor can be realized, which is of great industrial value.

Claims (1)

【特許請求の範囲】 (PbCa)TiO_3および(PbCa)(Mg_1
_/_2W_1_/_2)O_3よりなる磁器組成物を
、Pb_1_−_xCa_xTi_1_−_y(Mg_
1_/_2W_1_/_2)_yO_3と表したとき、
xおよびyがそれぞれ 0.4≦x≦0.6 0.2≦y≦0.5 の範囲にあることを特徴とする誘電体磁器組成物。
[Claims] (PbCa)TiO_3 and (PbCa)(Mg_1
_/_2W_1_/_2)O_3, Pb_1_-_xCa_xTi_1_-_y(Mg_
When expressed as 1_/_2W_1_/_2)_yO_3,
A dielectric ceramic composition characterized in that x and y are in the range of 0.4≦x≦0.6 and 0.2≦y≦0.5, respectively.
JP31224786A 1986-12-26 1986-12-26 Dielectric ceramic composition Pending JPS63166105A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP31224786A JPS63166105A (en) 1986-12-26 1986-12-26 Dielectric ceramic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP31224786A JPS63166105A (en) 1986-12-26 1986-12-26 Dielectric ceramic composition

Publications (1)

Publication Number Publication Date
JPS63166105A true JPS63166105A (en) 1988-07-09

Family

ID=18026935

Family Applications (1)

Application Number Title Priority Date Filing Date
JP31224786A Pending JPS63166105A (en) 1986-12-26 1986-12-26 Dielectric ceramic composition

Country Status (1)

Country Link
JP (1) JPS63166105A (en)

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