JPS63205005A - Alumina ceramic composition - Google Patents

Alumina ceramic composition

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Publication number
JPS63205005A
JPS63205005A JP62038533A JP3853387A JPS63205005A JP S63205005 A JPS63205005 A JP S63205005A JP 62038533 A JP62038533 A JP 62038533A JP 3853387 A JP3853387 A JP 3853387A JP S63205005 A JPS63205005 A JP S63205005A
Authority
JP
Japan
Prior art keywords
parts
weight
subcomponent
cao
mgo
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
JP62038533A
Other languages
Japanese (ja)
Other versions
JPH063684B2 (en
Inventor
安藤 汀
伊藤 幸昭
文夫 水野
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.)
Niterra Co Ltd
Original Assignee
NGK Spark Plug 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 NGK Spark Plug Co Ltd filed Critical NGK Spark Plug Co Ltd
Priority to JP62038533A priority Critical patent/JPH063684B2/en
Publication of JPS63205005A publication Critical patent/JPS63205005A/en
Publication of JPH063684B2 publication Critical patent/JPH063684B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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】 「産業上の利用分野」 本発明は通信機用のMIC基板、MICパッケージ、マ
イクロ波コンデンサ、あるいは高エネルギー粒子加速装
置のマイクロ波透過窓、クフイストロント外囲気等に適
した高周波低損失性のアルミナ磁器組成物に関する。
Detailed Description of the Invention "Field of Industrial Application" The present invention is applicable to MIC substrates for communication devices, MIC packages, microwave capacitors, microwave transmission windows of high-energy particle accelerators, and the outer air of Kufus Toronto. The present invention relates to a suitable high-frequency, low-loss alumina porcelain composition.

「発明が解決しようとする問題点」 上記の高周波低損失性のアルミナ磁器組成物として本出
願人は先に特願昭60−28792号(特開昭61−1
8816号)にオイてAl2O3−8i02− CaO
−MgO系について提案したが、更に進行・する通信周
波数の高周波化に対しては必ずしも満足すべき低誘電損
失が得難がった。
"Problems to be Solved by the Invention" The present applicant has previously published Japanese Patent Application No. 60-28792 (Japanese Unexamined Patent Application Publication No. 61-198) for the above-mentioned high-frequency low-loss alumina porcelain composition.
No. 8816), Al2O3-8i02- CaO
-MgO system was proposed, but it was difficult to obtain a satisfactory low dielectric loss as communication frequencies continue to advance.

「問題点を解決するための手段」 主成分のA l z Osを100重量部とし、これに
対して別紙8成分系組成図のA、B、C及びDで囲まれ
る4辺形区域内に打点される5in2゜CaO及びMg
Oの1種又は2種以上を第1の副成分、!−シ0.05
〜0.5 lim部ト、NbzOs k ’its 2
の副成分として0.05〜5.0重量部の割合で添加、
含有させることによって満足すべき特性を得ることがで
きた。
"Means for solving the problem" The main component AlzOs is 100 parts by weight, and in the quadrilateral area surrounded by A, B, C, and D in the attached 8-component system composition diagram. Dotted 5in2゜CaO and Mg
One or more types of O as the first subcomponent,! -shi0.05
~0.5 lim part, NbzOsk'its 2
Added as a subcomponent in a proportion of 0.05 to 5.0 parts by weight,
Satisfactory properties could be obtained by including the compound.

「作用」 主成分のAl2O3に対する第1の副成分5iOz。"action" The first subcomponent is 5 iOz with respect to the main component Al2O3.

CaO及びMgOは第2成分NbzOsとの組合せによ
って誘電損失を著しく改善する。。
CaO and MgO, in combination with the second component NbzOs, significantly improve dielectric loss. .

しかして、第1の副成分としては上記4辺形区域内にお
いてはMgO単独・、MgOと5iOzとの2成分のみ
においても有効であるが、該第1の副成物の主成分A 
I203に対する割合が0.05重景部よりも小さいと
きは効果を生ぜず、また逆に0.5重量部を越えた場合
もその効果を失う。
Therefore, as the first subcomponent, MgO alone or only the two components of MgO and 5iOz are effective within the quadrilateral area, but the main component A of the first subcomponent is effective.
If the ratio to I203 is smaller than 0.05 parts by weight, no effect will be produced, and conversely, if it exceeds 0.5 parts by weight, the effect will be lost.

一方、第2の副成分NbzOst主成分A l t O
sに対する割合が0.05重量部よシも小さいときは効
果が見られず、また逆に5.0重量部を超えるときは効
果を失なう。
On the other hand, the second subcomponent NbzOst and the main component A l t O
When the ratio to s is as small as 0.05 parts by weight, no effect is observed, and conversely, when it exceeds 5.0 parts by weight, the effect is lost.

「実施例」 (1)純度99.999%、平均粒径0.5μの市販の
A 120s粉末を主成分としてこれの10Ofに対し
、純度99.9%以上の市販の無水珪酸、炭酸力ρシウ
ム及び炭酸マグネシウムをそれぞれ最終生成物8LOz
 + CaO及びMgOに換算して別紙8成分系組成図
の各点の配合割合とした第1の副成分を0.22に、ま
た純度99.9%以上の5酸化ニオブ(NbzOs )
を第2の副成分として1.02に固定した15種の原料
粉末にそれぞれ水60mflを加え、50077i1Ω
のポリエチレン容器とゴムフィニングを施した15簡φ
の鉄製球石370?によって84rpm、48時間の混
合を行なった。
"Example" (1) Mainly composed of commercially available A 120s powder with a purity of 99.999% and an average particle size of 0.5μ, commercially available silicic anhydride with a purity of 99.9% or more and carbonic acid ρ 8LOz of final product each of sium and magnesium carbonate
+ The first subcomponent, which is converted into CaO and MgO and is the blending ratio of each point in the attached 8-component system composition diagram, is 0.22, and niobium pentoxide (NbzOs ) with a purity of 99.9% or more
60 mfl of water was added to each of the 15 raw material powders with 1.02 fixed as the second subcomponent, and 50077i1Ω
15mm diameter polyethylene container with rubber finning
Iron ball stone 370? Mixing was performed for 48 hours at 84 rpm.

ついで、各ロフトに対してポリビニルアルコ−1v1t
とポリエチレングリコ−/I’0.5fを加えて24時
間の溶解、混合を行ないスラリーを得た。
Then, for each loft, 1v1t of polyvinyl alcohol
and polyethylene glyco/I'0.5f were added and dissolved and mixed for 24 hours to obtain a slurry.

これらのスラリーを常法によって噴腸乾燥して凍原粉末
とし、1500 K9/dの金型プレスによって8瓢φ
X 8 M Lの素体に成形した後、電気炉の酸化性雰
囲気中において焼成した。
These slurries were dried in a conventional manner to obtain frozen ground powder, and then molded into 8 gourd φ with a mold press at 1500 K9/d.
After molding into an element body of X 8 M L, it was fired in an oxidizing atmosphere of an electric furnace.

約6.5 mφX6.5maLの各焼成品に研摩加工を
施し、脱イオン水中の超音波洗浄を行なっ九後、乾燥し
て得た15点のとなし、緒特性を測定した結果を第1表
に示す。
Each fired product of approximately 6.5 mφ x 6.5 maL was polished, subjected to ultrasonic cleaning in deionized water, and then dried. Table 1 shows the results of measuring the shape and strength of 15 points obtained. Shown below.

測定条件 マイクロ波帯における誘電体力率、誘 電率の測定は、誘電体円柱共振器法により、約15 G
Hzで行なった。
Measurement conditions The dielectric power factor and permittivity in the microwave band are measured using the dielectric cylindrical resonator method at approximately 15 G.
This was done at Hz.

また、共振周波数の温度係数は一20 〜+60゛Cの範囲で測定した。Also, the temperature coefficient of the resonant frequency is -20 Measurements were made in the range of ~+60°C.

第1表によりて明らかにされる通フ、主成分のAl2O
3L 00重量部に対し、第1の副成分となる5iOz
 、 CaO及びMgO8者の合量を0.2重量部、第
2の副成分NbzOs t−1,0重量部にそれぞれ固
定した上、上記第1の副成分となるSiO2,CaQ及
びMgO8者を種々の配合比とした場合、別紙8成分系
組成図においてA。
Tofu revealed by Table 1, main component Al2O
5iOz as the first subcomponent for 3L 00 parts by weight
, the total amount of CaO and MgO8 was fixed at 0.2 parts by weight, and the second subcomponent NbzOs was fixed at t-1.0 parts by weight, and the first subcomponent SiO2, CaQ and MgO8 were variously added. If the mixing ratio is A in the attached 8-component system composition diagram.

B、C及びDを順次結んだ4辺形区域内に打点される試
料NQ1〜10は区域外の試料、−11〜15に比して
著しく優れた誘電体力率を示した。
Samples NQ1 to NQ10, which were dotted within the rectangular area connecting B, C, and D in sequence, exhibited significantly superior dielectric power factors compared to samples -11 to 15 outside the area.

(2)前の火流側(1)と同様の条件によって、主成分
のAh03100重量部に対し、第1の副成分としてS
ing 、 CaO及びMgO8者の合意が前と同様に
0.2重量部、これら8者の配合比を別紙8成分系組成
図の略々中央に打点される試料−9のSing O,1
5、CaOO,05、Mg0O18の比率に固定し、第
2の副成分NbzOsを各種の重量部とした試料i1!
19a〜91の緒特性値を第2表に示す。
(2) Under the same conditions as in the previous fire flow side (1), S was added as the first subcomponent to 100 parts by weight of Ah03 as the main component.
ing, CaO, and MgO were agreed to be 0.2 parts by weight as before, and the blending ratio of these eight people was set approximately at the center of the attached eight-component system composition diagram, Sing O,1 of sample-9.
5. Sample i1 with a fixed ratio of CaOO,05, Mg0O18 and various weight parts of the second subcomponent NbzOs!
The initial characteristic values of Nos. 19a to 91 are shown in Table 2.

第1表において最も優れた誘電体力率を示した第1の副
成分8102 + CaO及びMgOの配合比を試料N
n9、またそれら3者の合量を0.2重量部にそれぞれ
固定し、第2の副成分NbzOaを種々の割合として配
合した場合、試料−9aと9bの関係から示されるよう
にNbzOsは0.08重量部の添加、含有によって誘
電体力率をA近くまで改曽するが、まだ不充分で少なく
とも0.05重量部を必要とし、1.0重f部の試料!
’Vil19fにおいて最大の効果を示し、かつ7.0
重量部の試料風91においては逆に劣化させ、0.05
〜5.0]ii部の9C〜9hにおいて満足すべき成果
を収めることが第2表から明らかにされる。
Sample N
n9, and when the total amount of these three is fixed at 0.2 parts by weight, and the second subcomponent NbzOa is mixed in various proportions, as shown from the relationship between Samples-9a and 9b, NbzOs is 0. By adding and containing 0.08 parts by weight, the dielectric power factor is improved to near A, but it is still insufficient and at least 0.05 parts by weight is required, and the sample is 1.0 parts by weight!
'Shows the greatest effect in Vil19f and 7.0
On the contrary, in the sample wind 91 of the weight part, it deteriorated to 0.05
~5.0] It is clear from Table 2 that satisfactory results were achieved in parts 9C to 9h of part ii.

(3)第2の副成分NbzOsを主成分AlzOs 1
00重量部に対し、tOW量部に固定、第1の剃成分5
iOz t CaO及びMgOを別紙3成分系組成図の
4辺形区域の略々中央に打点される隘9の比率に固定し
、その合量を上記AhOs 100重量部に対し、各種
の重量部とした他は前2例と同一条件で製作した試料N
119イ〜9ホの緒特性を第8表に示す。
(3) The second subcomponent NbzOs is the main component AlzOs 1
00 parts by weight, fixed at tOW parts, first shaving component 5
iOz t CaO and MgO are fixed at the ratio shown in box 9, which is dotted approximately at the center of the quadrilateral area in the attached ternary component system composition diagram, and the total amount is added to 100 parts by weight of AhOs in various parts by weight. Sample N was manufactured under the same conditions as the previous two examples except for
Table 8 shows the characteristics of 119A to 9E.

第1表の副成分5te21 CaO及びMgOの配合比
及び第2の副成分を最良の状態に固定し上記第1の副成
分の総量を変化させた場合、0.08重量部の試料IV
III19イでは誘電体力率に及ぼす効果が不充分、ま
た0、 7重量部の試料NQ9へは過剰に失し、0.0
5〜5.0重量部の試料N1190〜9ホにおいて満足
が得られ、特に0. I M置部の試料先9ハが最良を
示すことが第3表から明らかにされる。
Subcomponent 5te21 in Table 1 When the blending ratio of CaO and MgO and the second subcomponent are fixed at the best conditions and the total amount of the first subcomponent is varied, 0.08 parts by weight of sample IV
In III19a, the effect on the dielectric power factor was insufficient, and in sample NQ9 of 0.7 parts by weight, an excessive loss of 0.0 parts by weight occurred.
Satisfaction was obtained with samples N1190-9E containing 5 to 5.0 parts by weight, especially 0. It is clear from Table 3 that sample tip 9c of the IM placement section shows the best.

以上の過少、主成分のAlzOa 100重量部に対し
、第1の副成分として別紙8成分系組成図のA、B、C
及びDを順次結ぶ4辺形区域内にあジ、これら5tO2
,CaO及びMgOの1槌又は2種以上を0.05〜0
.5重量部と、第2の副成分としてNbzOsを0.5
〜5.0重量部とを併添、含有させてなる本発明の高ア
ルミナ磁器組成物は、焼結性(焼成温度)、誘電率及び
共振周波数の温度係数等信の緒特性に殆んど悪影響を与
えることなく、目的とする誘電体力率を大幅に改善する
優れた効果を奏する。
In the above case, for 100 parts by weight of the main component AlzOa, A, B, and C of the attached 8-component system composition diagram are added as the first subcomponent.
and D in a quadrilateral area sequentially connecting these 5tO2
, one or more of CaO and MgO from 0.05 to 0
.. 5 parts by weight and 0.5 parts by weight of NbzOs as a second subcomponent.
The high alumina porcelain composition of the present invention containing ~5.0 parts by weight has almost no reliable characteristics such as sinterability (firing temperature), dielectric constant, and temperature coefficient of resonance frequency. It has an excellent effect of significantly improving the target dielectric power factor without causing any adverse effects.

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

図面は本発明の高アルミナ磁器組成物中、第1の副成分
とする8102 + CaO及びMgOの配合割合を示
す8成分系組成図である。
The drawing is an 8-component system composition diagram showing the blending ratio of 8102 + CaO and MgO as the first subcomponents in the high alumina ceramic composition of the present invention.

Claims (1)

【特許請求の範囲】 主成分のAl_2O_3100重量部に対し、第1の副
成分として別紙3成分系組成図の ▲数式、化学式、表等があります▼ からなるA〜Dを逐次結ぶ4辺形区域内にありこれらS
iO_2、CaO及びMgOの1種又は2種以上を0.
05〜0.5重量部と、第2の副成分としてNb_2O
_5を0.5〜5重量部とを添加、含有させてなる高ア
ルミナ磁器組成物。
[Scope of Claims] For 100 parts by weight of Al_2O_3 as the main component, the first subcomponent is a quadrilateral area sequentially connecting A to D in the attached three-component system composition diagram ▲ mathematical formulas, chemical formulas, tables, etc. ▼ These S
One or more of iO_2, CaO, and MgO was added to 0.
05 to 0.5 parts by weight and Nb_2O as a second subcomponent
A high alumina porcelain composition containing _5 in an amount of 0.5 to 5 parts by weight.
JP62038533A 1987-02-20 1987-02-20 Alumina porcelain composition Expired - Lifetime JPH063684B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP62038533A JPH063684B2 (en) 1987-02-20 1987-02-20 Alumina porcelain composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP62038533A JPH063684B2 (en) 1987-02-20 1987-02-20 Alumina porcelain composition

Publications (2)

Publication Number Publication Date
JPS63205005A true JPS63205005A (en) 1988-08-24
JPH063684B2 JPH063684B2 (en) 1994-01-12

Family

ID=12527917

Family Applications (1)

Application Number Title Priority Date Filing Date
JP62038533A Expired - Lifetime JPH063684B2 (en) 1987-02-20 1987-02-20 Alumina porcelain composition

Country Status (1)

Country Link
JP (1) JPH063684B2 (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2288597A (en) * 1994-04-20 1995-10-25 Kyocera Corp Alumina sintered product

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5747767A (en) * 1980-09-08 1982-03-18 Ngk Spark Plug Co Low friction alumina ceramic

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5747767A (en) * 1980-09-08 1982-03-18 Ngk Spark Plug Co Low friction alumina ceramic

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2288597A (en) * 1994-04-20 1995-10-25 Kyocera Corp Alumina sintered product
GB2288597B (en) * 1994-04-20 1998-01-28 Kyocera Corp Alumina sintered product
US5830819A (en) * 1994-04-20 1998-11-03 Kyocera Corporation Alumina sintered product

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Publication number Publication date
JPH063684B2 (en) 1994-01-12

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