JPH0873266A - Production of dielectric ceramic - Google Patents

Production of dielectric ceramic

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Publication number
JPH0873266A
JPH0873266A JP6207729A JP20772994A JPH0873266A JP H0873266 A JPH0873266 A JP H0873266A JP 6207729 A JP6207729 A JP 6207729A JP 20772994 A JP20772994 A JP 20772994A JP H0873266 A JPH0873266 A JP H0873266A
Authority
JP
Japan
Prior art keywords
firing
powder
dielectric
dielectric ceramic
ceramic
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.)
Withdrawn
Application number
JP6207729A
Other languages
Japanese (ja)
Inventor
Satohiko Memezawa
聡彦 目々澤
Keiichi Kagami
慶一 鏡
Takeshi Segawa
健 瀬川
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.)
Sony Corp
Original Assignee
Sony Corp
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 Sony Corp filed Critical Sony Corp
Priority to JP6207729A priority Critical patent/JPH0873266A/en
Publication of JPH0873266A publication Critical patent/JPH0873266A/en
Withdrawn legal-status Critical Current

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Abstract

PURPOSE: To obtain an MgTiO3 -CaTiO3 based dielectric ceramic improved in low-loss characteristic or the like by firing the powder of raw materials with the specific control of firing temp. and firing time after mixing, calcining, pulverizing and press molding. CONSTITUTION: The powder of the raw materials such as TiO2 , MgO or CaCO3 is weighed and wetly mixed so as to obtain a desired composition. Next, the mixture is dried, pulverized and after that, calcined in a kiln at about 1100 deg.C in an oxygen atmosphere. Next, the ceramic after calcined is dried and granulated by adding a binder for molding, after pulverized and secondarily mixed to adjust the powder particle diameter. Next, the MgTiO3 -CaTiO3 based dielectric ceramic is obtained by press molding the granulated powder and firing in the kiln at 1200-1250 deg.C in the oxygen atmosphere for 2-5hr. The obtained dielectric ceramic is suitably used for a dielectric antenna for high frequency or the like.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は例えば高周波(マイクロ
波)用の誘電体アンテナ、誘電体共振器等に使用して好
適な誘電体セラミクスの製造方法に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a method for producing a dielectric ceramic suitable for use in, for example, a high frequency (microwave) dielectric antenna, a dielectric resonator, or the like.

【0002】[0002]

【従来の技術及び発明が解決しようとする課題】近年、
高周波(マイクロ波)用の誘電体アンテナ、誘電体共振
器等の如き電子デバイスの小型化、高周波化、高性能化
にともないマイクロ波域で高誘電率でかつ低損失である
誘電体セラミクスが必要とされている。
2. Description of the Related Art In recent years,
Dielectric ceramics with high permittivity and low loss in the microwave region are required as electronic devices such as high-frequency (microwave) dielectric antennas and dielectric resonators become smaller, higher in frequency, and higher in performance. It is said that.

【0003】従来、この高誘電率で低損失である誘電体
セラミクスとしてMgTiO3 −CaTiO3 系の誘電
体セラミクスが知られている(エレクトロニクス・セラ
ミクス 1993,Vol.24,124号)。このM
gTiO3 −CaTiO3 系の誘電体セラミクスの特性
は誘電率ε=21でQf(Q値に共振周波数fを乗算し
た値)=56000GHzである。
Conventionally, MgTiO 3 —CaTiO 3 -based dielectric ceramics have been known as the dielectric ceramics having a high dielectric constant and low loss (Electronics Ceramics 1993, Vol. 24, 124). This M
The characteristics of the gTiO 3 —CaTiO 3 system dielectric ceramics are dielectric constant ε = 21 and Qf (Q value multiplied by resonance frequency f) = 56000 GHz.

【0004】この従来のMgTiO3 −CaTiO3
の誘電体セラミクスの製造方法は、図3に示す如く、先
ずTiO2 ,MgO,CaCO3 の原料粉末を(Mg
0.95Ca0.05)TiO3 で示される組成に秤量し、ボー
ルミル等で1次混合し、その後乾燥し、これを粉砕す
る。これを1000℃〜1200℃の温度で仮焼し、こ
の仮焼後のセラミクスを再び粉砕し、その後、これを2
次混合し、これを乾燥し、その後造粒する。この造粒し
たものにバインダー(PVA)を添加し、加圧成形し、
この成形体を1400℃〜1600℃で焼成した。
As shown in FIG. 3, this conventional method of manufacturing a MgTiO 3 --CaTiO 3 -based dielectric ceramics first comprises forming raw material powders of TiO 2 , MgO, and CaCO 3 into (Mg
0.95 Ca 0.05 ) TiO 3 is weighed, primary mixed with a ball mill or the like, then dried and crushed. This is calcined at a temperature of 1000 ° C. to 1200 ° C., and the ceramics after the calcining are pulverized again, and thereafter, this is
Then mix, dry it and then granulate. A binder (PVA) is added to this granulated product, and pressure molding is performed.
This compact was fired at 1400 ° C to 1600 ° C.

【0005】このようにして製造された従来のMgTi
3 −CaTiO3 系の誘電体セラミクスの特性は誘電
率ε=21で且つQf=56000GHzであった。
Conventional MgTi produced in this way
The characteristics of the O 3 -CaTiO 3 -based dielectric ceramics were a dielectric constant ε = 21 and Qf = 56000 GHz.

【0006】本発明は斯る点に鑑み、更に特性を向上し
た誘電体セラミクスを得ることを目的とする。
In view of the above points, the present invention has an object to obtain a dielectric ceramics having further improved characteristics.

【0007】[0007]

【課題を解決するための手段】本発明誘電体セラミクス
の製造方法は少なくとも原料粉末の混合工程、仮焼工
程、粉砕工程、加圧成形工程、焼成工程を経て製造する
MgTiO3 −CaTiO3 系の誘電体セラミクスの製
造方法において、この焼成工程における焼成温度を12
00℃〜1250℃とし且つ焼成時間を2時間〜5時間
としたものである。
The method for producing a dielectric ceramics of the present invention is based on at least a MgTiO 3 --CaTiO 3 system produced by a raw material powder mixing step, a calcination step, a crushing step, a pressure molding step, and a firing step. In the method for producing a dielectric ceramic, the firing temperature in this firing step is set to 12
The temperature is set to 00 ° C to 1250 ° C and the firing time is set to 2 hours to 5 hours.

【0008】[0008]

【作用】斯る本発明によれば誘電体セラミクスのQf値
が略69000GHzのものが得られ、それだけ特性が
改善される。
According to the present invention, a dielectric ceramic having a Qf value of approximately 69000 GHz is obtained, and the characteristics are improved accordingly.

【0009】[0009]

【実施例】以下図面を参照しながら本発明誘電体セラミ
クスの製造方法の一実施例につき説明する。本例の誘電
体セラミクスの製造方法の製造工程も図3に示す如くで
ある。
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS An embodiment of the method for producing dielectric ceramics of the present invention will be described below with reference to the drawings. The manufacturing process of the method for manufacturing dielectric ceramics of this example is also as shown in FIG.

【0010】本例においては、先ずTiO2 ,MgO,
CaCO3 の原料粉末を(Mg0.95Ca0.05)TiO3
で示される組成に秤量し、これをボールミルで15時間
湿式混合(1次混合)する。この湿式混合後これを乾燥
機を使用し、100℃で20時間乾燥し、これを粉砕す
る。
In this example, first, TiO 2 , MgO,
The raw material powder of CaCO 3 is (Mg 0.95 Ca 0.05 ) TiO 3
Is weighed to a composition shown by and wet-mixed (primary mixing) for 15 hours with a ball mill. After this wet mixing, this is dried at 100 ° C. for 20 hours using a drier and then pulverized.

【0011】次にこの粉砕した粉末を仮焼する。この仮
焼はジルコニアるつぼを用いて焼成炉で1100℃,5
時間,O2 雰囲気中で行う。
Next, the pulverized powder is calcined. This calcination was performed at 1100 ° C. for 5 hours in a firing furnace using a zirconia crucible.
Time, O 2 atmosphere.

【0012】この仮焼後のセラミクスを粉砕し、2次混
合することにより粉末粒子径を調整する。この仮焼後の
粉末を乾燥し、その後この仮焼後の粉末に成形用のバイ
ンダーとしてPVA10%の水溶液を10%添加し、#
28のふるいで分級し、これを造粒粉とする。
The calcinated ceramics are crushed and secondarily mixed to adjust the powder particle size. The powder after the calcination is dried, and then 10% aqueous solution of PVA is added as a molding binder to the powder after the calcination.
Classify with a No. 28 sieve and use this as granulated powder.

【0013】この造粒粉を水分調整して、プレス圧8.
2MPa,加圧時間200秒で加圧成形を行う。この成
形体を焼成炉を用いてO2 雰囲気中で、図1に示す如く
焼成温度及び焼成時間を変化させて焼成を行った。
The granulated powder is adjusted for water content and pressed at a pressure of 8.
Pressure molding is performed at a pressure of 2 MPa for 200 seconds. This molded body was fired in an O 2 atmosphere using a firing furnace while changing the firing temperature and firing time as shown in FIG.

【0014】この焼成温度としては1100℃,120
0℃,1250℃,1300℃,1350℃とし、それ
ぞれ0〜10時間焼成した。
The firing temperature is 1100 ° C., 120
The temperature was 0 ° C., 1250 ° C., 1300 ° C., and 1350 ° C., and the firing was performed for 0 to 10 hours.

【0015】この場合焼成セラミクスを直径19mm,
厚さ7.6mmの円柱に加工し、誘電体共振器法により
測定周波数3GHz〜6GHzの範囲で共振周波数fと
そのQ値を測定し、これからQf値を算出した。この結
果を図1に示す。また図2に本例により製造した誘電体
セラミクスの誘電率εと焼成時間との関係を示す。
In this case, the firing ceramic has a diameter of 19 mm,
It was processed into a cylinder having a thickness of 7.6 mm, the resonance frequency f and its Q value were measured in the range of measurement frequency 3 GHz to 6 GHz by the dielectric resonator method, and the Qf value was calculated from this. The result is shown in FIG. FIG. 2 shows the relationship between the dielectric constant ε and the firing time of the dielectric ceramics manufactured according to this example.

【0016】この図1,図2の結果よりして焼成工程に
おける焼成温度が1200℃〜1250℃で、焼成時間
が2時間〜5時間の条件で製造した上述の誘電体セラミ
クスは誘電率εが従来と同等で21と高く且つQf値が
略69000GHzに改善されている。
From the results shown in FIGS. 1 and 2, the above-mentioned dielectric ceramics manufactured under the conditions that the firing temperature in the firing step is 1200 ° C. to 1250 ° C. and the firing time is 2 hours to 5 hours have a dielectric constant ε. It is 21 as high as the conventional one and the Qf value is improved to about 69000 GHz.

【0017】以上述べた如く本例によれば(Mg0.95
0.05)TiO3 の誘電体セラミクスの焼成工程におけ
る焼成温度を1200℃〜1250℃とし且つ焼成時間
を2時間〜5時間としているのでQf値が略69000
GHzのものが得られ、それだけ特性が改善された、即
ちそれだけ低損失の誘電体セラミクスが得られる利益が
ある。
As described above, according to this example, (Mg 0.95 C
a 0.05 ) Since the firing temperature in the firing process of the dielectric ceramic of TiO 3 is 1200 ° C. to 1250 ° C. and the firing time is 2 hours to 5 hours, the Qf value is about 69000.
There is an advantage that a dielectric material ceramics of GHz is obtained and the characteristics thereof are improved, that is, the dielectric ceramics of lower loss are obtained.

【0018】尚本発明は上述実施例に限ることなく本発
明の要旨を逸脱することなく、その他種々の構成が採り
得ることは勿論である。
The present invention is not limited to the above-mentioned embodiments, and it goes without saying that various other configurations can be adopted without departing from the gist of the present invention.

【0019】[0019]

【発明の効果】本発明によればQf値即ち低損失特性の
改善された誘電体セラミクスを得ることができる利益が
ある。
According to the present invention, there is an advantage that a dielectric ceramic having an improved Qf value, that is, a low loss characteristic can be obtained.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の説明に供する線図である。FIG. 1 is a diagram for explaining the present invention.

【図2】本発明の説明に供する線図である。FIG. 2 is a diagram for explaining the present invention.

【図3】誘電体セラミクスの製造工程を示す線図であ
る。
FIG. 3 is a diagram showing a manufacturing process of dielectric ceramics.

Claims (1)

【特許請求の範囲】[Claims] 【請求項1】 少なくとも原料粉末の混合工程、仮焼工
程、粉砕工程、加圧成形工程、焼成工程を経て製造する
MgTiO3 −CaTiO3 系の誘電体セラミクスの製
造方法において、 前記焼成工程における焼成温度を1200℃〜1250
℃とし且つ焼成時間を2時間〜5時間としたことを特徴
とする誘電体セラミクスの製造方法。
1. A method for producing a MgTiO 3 —CaTiO 3 -based dielectric ceramics, which is produced through at least a raw material powder mixing step, a calcination step, a crushing step, a pressure molding step, and a firing step. Temperature 1200 ℃ ~ 1250
The method for producing a dielectric ceramics is characterized in that the temperature is set to 0 ° C. and the firing time is set to 2 hours to 5 hours.
JP6207729A 1994-08-31 1994-08-31 Production of dielectric ceramic Withdrawn JPH0873266A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP6207729A JPH0873266A (en) 1994-08-31 1994-08-31 Production of dielectric ceramic

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP6207729A JPH0873266A (en) 1994-08-31 1994-08-31 Production of dielectric ceramic

Publications (1)

Publication Number Publication Date
JPH0873266A true JPH0873266A (en) 1996-03-19

Family

ID=16544578

Family Applications (1)

Application Number Title Priority Date Filing Date
JP6207729A Withdrawn JPH0873266A (en) 1994-08-31 1994-08-31 Production of dielectric ceramic

Country Status (1)

Country Link
JP (1) JPH0873266A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0856489A1 (en) * 1997-01-31 1998-08-05 Kubota Corporation Powder of titanium compounds
CN109206134A (en) * 2018-10-24 2019-01-15 天津大学 A kind of preparation method of high quality factor magnesium titanate base microwave medium ceramics

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0856489A1 (en) * 1997-01-31 1998-08-05 Kubota Corporation Powder of titanium compounds
US5962551A (en) * 1997-01-31 1999-10-05 Kubota Corporation Powder of titanium compounds
CN109206134A (en) * 2018-10-24 2019-01-15 天津大学 A kind of preparation method of high quality factor magnesium titanate base microwave medium ceramics

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