JPS5957955A - Ceramic composition - Google Patents

Ceramic composition

Info

Publication number
JPS5957955A
JPS5957955A JP57167822A JP16782282A JPS5957955A JP S5957955 A JPS5957955 A JP S5957955A JP 57167822 A JP57167822 A JP 57167822A JP 16782282 A JP16782282 A JP 16782282A JP S5957955 A JPS5957955 A JP S5957955A
Authority
JP
Japan
Prior art keywords
porcelain
main component
temperature
composition
practical
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
JP57167822A
Other languages
Japanese (ja)
Other versions
JPH0360789B2 (en
Inventor
治彦 宮本
米沢 正智
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.)
NEC Corp
Original Assignee
Nippon Electric 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 Nippon Electric Co Ltd filed Critical Nippon Electric Co Ltd
Priority to JP57167822A priority Critical patent/JPS5957955A/en
Publication of JPS5957955A publication Critical patent/JPS5957955A/en
Publication of JPH0360789B2 publication Critical patent/JPH0360789B2/ja
Granted 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】 本発明は、磁器組成物、特に1000°0以下の低温で
焼結でき、誘電率が高く、誘電損失が小さく、絶縁抵抗
が高く、シかも機械的強度の高い磁器組成物に関するも
のである。
DETAILED DESCRIPTION OF THE INVENTION The present invention provides a porcelain composition, particularly a porcelain composition that can be sintered at a low temperature of 1000° or less, has a high dielectric constant, low dielectric loss, high insulation resistance, and high mechanical strength. The present invention relates to a composition.

従来、誘電体磁器組成物として、チタン酸バリウム(B
aTi03 )f主成分とする磁器て広く実用化されて
いることは周知のとおりである。しかしながら、チタン
酸バリウム(BaTi03 )f主成分とするものは、
焼結温度が通常1300〜1400℃の高温である。こ
のためこれ全積層形コンデンサに利用する場合には内部
電極としてこの焼結温度に耐え得る材料、例えば白金、
パラジウムなどの高価な貴金属を使用しなければならず
、製造コストが高くつくという欠点がある。積層形コン
デンサを安く作るためには、銀、ニッケルなどを主成分
とする安価な金属が内部電極に使用できるような、でき
るだけ低温、特に1000°C以下で焼結できる磁器が
必要である。
Conventionally, barium titanate (B
It is well known that porcelain containing aTi03) f as its main component is widely put into practical use. However, the main component of barium titanate (BaTi03) is
The sintering temperature is usually a high temperature of 1300 to 1400°C. Therefore, when used in a fully laminated capacitor, it is necessary to use a material that can withstand this sintering temperature for the internal electrode, such as platinum.
The drawback is that expensive precious metals such as palladium must be used, resulting in high manufacturing costs. In order to manufacture multilayer capacitors at low cost, it is necessary to use porcelain that can be sintered at as low a temperature as possible, especially below 1000°C, so that inexpensive metals mainly composed of silver and nickel can be used for the internal electrodes.

また、磁器組成物の電気的特性として、誘電率が高く、
誘電損失が小さく、絶縁抵抗が高いことが基本的に要求
される。
In addition, the electrical properties of the porcelain composition include a high dielectric constant,
Basically, it is required to have low dielectric loss and high insulation resistance.

また、積層形チップコンデンサの場合は、チップコンデ
ンサを基板に実装したとき、基板とチップコンデンサを
構成している磁器との熱膨張係数の違いにより、チップ
コンデンサに機械的な歪が加わり、チップコンデンサに
クラックが発生したシ、破損したフすることがある。ま
たエポキシ系樹脂等全外装したディップコンデンサの場
合も外装樹脂の応力でディップコンデンサにクラックが
発生する場合がある。いずれの場合もコンデンサを形成
している磁器の械械的一度が低いほど、クラックが入り
やすく容易に破損するため、信頼性が低くなる。したが
って、磁器の機械的強度をできるだけ増大させることは
実用上極めて重要なことである。
In addition, in the case of multilayer chip capacitors, when the chip capacitor is mounted on a board, mechanical strain is applied to the chip capacitor due to the difference in thermal expansion coefficient between the board and the porcelain that makes up the chip capacitor. If cracks occur on the product, it may become damaged. In addition, even in the case of a dip capacitor entirely coated with epoxy resin or the like, cracks may occur in the dip capacitor due to the stress of the coating resin. In either case, the lower the mechanical strength of the porcelain forming the capacitor, the more likely it is to crack and break, resulting in lower reliability. Therefore, it is of practical importance to increase the mechanical strength of porcelain as much as possible.

本発明の目的は900〜1000℃の低温領域で焼結で
き、誘電率が高く、誘電損失が小さく、絶縁抵抗が高い
優れた電気的特性を有し、更に機械的強度も大きい信頼
性の高い磁器組成物全提供することにある。
The purpose of the present invention is to sinter in the low temperature range of 900 to 1000°C, have excellent electrical properties such as high dielectric constant, low dielectric loss, and high insulation resistance, and also have high mechanical strength and high reliability. There is a whole range of porcelain compositions to offer.

本発明の磁器組成物は、ニッケル・タングステン夷わし
たとさの主成分配合比Xが030≦X≦0.60の範囲
内にある主成分組成物に、副成分としてマンガン・ニオ
ブ酸鉛(P b、(Mn 1 /3 Nb 2 /3 
) 03)を前記主成分組成物に対して0.05〜8m
01%添加含有せしめてなることを特徴とする。
The porcelain composition of the present invention has a main component composition in which the main component blend ratio X of nickel and tungsten is within the range of 030≦X≦0.60, and manganese lead niobate (lead niobate) as a subcomponent. P b, (Mn 1 /3 Nb 2 /3
) 03) in an amount of 0.05 to 8 m relative to the main component composition.
It is characterized by containing 0.01% additive.

以下、本発明をその実施例により詳細に説明する。Hereinafter, the present invention will be explained in detail with reference to examples thereof.

出発原料として純度99.9%以上の酸化鉛(PbOλ
酸化ニッケル(NtO)、酸化タングステン(WOs)
Lead oxide (PbOλ) with a purity of 99.9% or more is used as a starting material.
Nickel oxide (NtO), tungsten oxide (WOs)
.

酸化チタン(T 10x ) m酸化ニオブ(Nb2 
Us )および炭酸マンガン(MnCOs )2使用し
、第1図に示した配合比となるように各々秤量する。次
に秤量した各材料をボールミル中で湿式混合した後、7
50〜800°Cで予焼全行ない、この粉末をボールミ
ルで粉砕し、日別、乾燥後、有機バインダーを入れ、整
粒後プレスし、直径15mm、厚さ約2mmの円板4枚
と、直径15mm、厚さ約IQmmの円柱を作製した。
Titanium oxide (T 10x ) Niobium oxide (Nb2
Us ) and manganese carbonate (MnCOs ) 2 were used, and each was weighed so that the mixing ratio shown in FIG. 1 was achieved. Next, after wet mixing the weighed materials in a ball mill,
Complete pre-baking at 50-800°C, pulverize this powder with a ball mill, dry it daily, add an organic binder, size it and press it to form 4 discs with a diameter of 15 mm and a thickness of about 2 mm. A cylinder having a diameter of 15 mm and a thickness of approximately IQ mm was prepared.

次に空気中900〜1000°Cの温度で1時間焼結し
た。焼結した円板4枚の上下面に600°Cで銀電極全
焼付け、デジタルLCRメーターで周波数IKHz、1
Jt、圧IVr−m−s温度20℃で各組。
Next, it was sintered in air at a temperature of 900-1000°C for 1 hour. Silver electrodes were completely baked on the top and bottom surfaces of four sintered disks at 600°C, and a frequency of IKHz, 1 was measured using a digital LCR meter.
Jt, pressure IV r-m-s temperature 20°C for each set.

と誘電損失を測足し、誘電率を算出した。次に超絶縁抵
抗計で50Vの電圧を1分間印加して絶縁抵抗を温度2
0℃で測定し、比抵抗を算出した。
The dielectric loss was measured and the dielectric constant was calculated. Next, apply a voltage of 50V for 1 minute using a super insulation resistance tester to measure the insulation resistance at a temperature of 2.
It was measured at 0°C and the specific resistance was calculated.

機械的性質全抗折強度で評価するため、焼結した円柱か
ら厚さQ、5mm、幅2 mm、長さ13mmの矩形板
を10枝切り出した。支点間距離i9mmVCより、(
Kg/cm2)なる式に従い、抗折強度r (K g/
cm 21を求めた。ただし1は支点間距離、tは試料
の厚み、Wは試料の幅である。電気的特性は円板試料4
点の平均値、抗折強度は矩形板試料10点の平均値よ)
求めた。
Mechanical properties In order to evaluate the total bending strength, ten rectangular plates each having a thickness Q of 5 mm, a width of 2 mm, and a length of 13 mm were cut out from the sintered cylinder. From the fulcrum distance i9mmVC, (
According to the formula: Kg/cm2), the bending strength r (Kg/cm2)
cm 21 was determined. However, 1 is the distance between the supporting points, t is the thickness of the sample, and W is the width of the sample. Electrical characteristics are disk sample 4
The average value of points, the bending strength is the average value of 10 rectangular plate samples)
I asked for it.

このようにして得られた磁器組成物の主成分〔Pb(N
i□/ 2 Wl /2 )03)X  (”bTiO
3)□−8の配合比Xおよび副成分添加量と誘電率、誘
電損失。
The main component of the porcelain composition thus obtained [Pb(N
i□/2 Wl /2 )03)X ("bTiO
3) Mixing ratio X of □-8, additive amount of subcomponents, dielectric constant, and dielectric loss.

比抵抗および抗折強度の関係を第1図に示す。なお、試
料番号に*印を付したものは本発明に含まれない。
The relationship between specific resistance and bending strength is shown in FIG. Note that sample numbers marked with * are not included in the present invention.

この結果から明らかなように、本発明によれば、誘電率
が1200〜7000と高く、誘電損失が0.3〜2.
2%と小さく、比抵抗が5X10”〜4×1013Ω・
cmという高い値を示し、さらに抗折強度も990〜1
410kg/Cm と実用上十分高い値を示す信頼性の
高い実用性の極めて高い磁器組成物が得られる。こうし
た優れた特性を示す本発明の磁粉は焼結温度が1000
℃以下の低温であるため積層コンデンサの内部電極の低
価格化を実現できると共に、省エネルギーや炉材の節約
にもなるという極めて優れた効果も生じる。なお、主成
分配合比XはX<0.30ではキュリ一温度が実用範囲
よシ高くなりすぎ室温での誘電率が小さくなり、また誘
電損失も大きくなるため実用的でない。X>0.60で
は磁器として焼結せず実用的でない。また副成分である
P b (Mn 1/a Nb 2 /3 ) 03 
O添710 鞭カ0.05malt%未満では抗折強度
の改善効果が小さく、8mo7%を超えると逆に抗折強
度が小さくなるため実用的でない。
As is clear from these results, according to the present invention, the dielectric constant is as high as 1,200 to 7,000, and the dielectric loss is as high as 0.3 to 2.
It is as small as 2% and has a specific resistance of 5X10” to 4×1013Ω・
It shows a high value of cm, and also has a bending strength of 990 to 1.
A highly reliable and highly practical porcelain composition having a value of 410 kg/Cm, which is sufficiently high for practical use, can be obtained. The magnetic powder of the present invention exhibiting these excellent properties has a sintering temperature of 1000
Since the temperature is low, below ℃, it is possible to reduce the cost of the internal electrodes of multilayer capacitors, and it also has the extremely excellent effect of saving energy and furnace materials. If the main component compounding ratio X is less than 0.30, the Curie temperature will be too high than the practical range, the dielectric constant at room temperature will be small, and the dielectric loss will also be large, which is not practical. If X>0.60, it will not be sintered as porcelain and is not practical. In addition, the subcomponent P b (Mn 1/a Nb 2 /3) 03
If the O addition 710 concentration is less than 0.05 malt%, the effect of improving the bending strength is small, and if it exceeds 8mo7%, the bending strength becomes small, which is not practical.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図は本発明の実施例における特性を示す[である。 代理人 弁理士  内 原   音 手続補正書(自発) 特許庁長官 殿 1、事件の表示   昭和57年特許  願第1678
22号2、発明の名称   磁器組成物 3、補正をする者 事件との関係       出 願 人東京都港区芝五
丁目33番1号 (423)   日本電気株式会社 代表者 関本忠弘 4、代理人 〒108  東京都港区芝五丁]]37番8号 住人三
田ビル5、補正の対象 明細書の発明の詳細な説明の欄 6、補正の内容 (1)  明細書の第2頁第2行目K「磁器て」とある
のを「磁器が」と補正する。
FIG. 1 shows the characteristics of an embodiment of the present invention. Agent Patent Attorney Original Sound Procedural Amendment (Voluntary) Commissioner of the Patent Office 1, Indication of Case 1982 Patent Application No. 1678
No. 22 No. 2, Title of the invention: Porcelain composition 3, Relationship to the amended person's case Applicant: 5-33-1 Shiba, Minato-ku, Tokyo (423) NEC Corporation Representative: Tadahiro Sekimoto 4, Agent: 108 Shiba Go-cho, Minato-ku, Tokyo] 37-8 Resident Mita Building 5, Detailed explanation of the invention column 6 of the specification subject to amendment, Contents of amendment (1) Page 2, line 2 of the specification K Correct ``porcelain te'' to ``porcelain ga''.

Claims (1)

【特許請求の範囲】[Claims] ニッケル・タンゲスf 7 M (P b(N il 
/2W1/2)03)  とチタン酸鉛(PbTi03
)を主成分としくp b (N I L /2 W 1
 /2 ) 03)X (P b T io 3)1−
Xと表わしたときの主成分配合比Xが0,30≦X≦0
.60の範囲内にある主成分組成物に、副成分としてマ
ンガン・ニオブ酸鉛(Pb(Mn1/a Nb2/3)
03)を前記主成分組成物に対して0.05〜8mO!
チ添加含有せしめてなることを特徴とする磁器組成物。
Nickel tongue f 7 M (P b(N il
/2W1/2)03) and lead titanate (PbTi03
) as the main component and p b (N I L /2 W 1
/2) 03)X (P b T io 3) 1-
The main component blending ratio X, expressed as X, is 0.30≦X≦0
.. Manganese lead niobate (Pb (Mn1/a Nb2/3)
03) to 0.05 to 8 mO to the main component composition!
A porcelain composition characterized in that it contains an additive.
JP57167822A 1982-09-27 1982-09-27 Ceramic composition Granted JPS5957955A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP57167822A JPS5957955A (en) 1982-09-27 1982-09-27 Ceramic composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP57167822A JPS5957955A (en) 1982-09-27 1982-09-27 Ceramic composition

Publications (2)

Publication Number Publication Date
JPS5957955A true JPS5957955A (en) 1984-04-03
JPH0360789B2 JPH0360789B2 (en) 1991-09-17

Family

ID=15856733

Family Applications (1)

Application Number Title Priority Date Filing Date
JP57167822A Granted JPS5957955A (en) 1982-09-27 1982-09-27 Ceramic composition

Country Status (1)

Country Link
JP (1) JPS5957955A (en)

Also Published As

Publication number Publication date
JPH0360789B2 (en) 1991-09-17

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