JPH0597511A - Porcelain composition - Google Patents
Porcelain compositionInfo
- Publication number
- JPH0597511A JPH0597511A JP3253689A JP25368991A JPH0597511A JP H0597511 A JPH0597511 A JP H0597511A JP 3253689 A JP3253689 A JP 3253689A JP 25368991 A JP25368991 A JP 25368991A JP H0597511 A JPH0597511 A JP H0597511A
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- mol
- composition
- temperature coefficient
- dielectric constant
- dielectric
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- Inorganic Insulating Materials (AREA)
Abstract
(57)【要約】
【目的】 高誘電率、低損失で、誘電率の温度係数が任
意に制御でき、かつ、安定な、高周波帯域における電子
部品の誘電体として使用できる磁気組成物を提供する。
【構成】 xMgO+yCaO+zTiO2+uCr2O3と
して表され、x,y,z,uがそれぞれ、25≦x≦ 80
(mol%),1≦y≦5(mol%),10≦z≦70(mol%),0.5
<u≦10(mol%)を満足する組成を有する磁器組成物。(57) [Abstract] [PROBLEMS] To provide a magnetic composition having a high dielectric constant, a low loss, a temperature coefficient of the dielectric constant which can be arbitrarily controlled, and which can be used as a dielectric of an electronic component in a high frequency band in a stable manner. . [Structure] xMgO + yCaO + zTiO 2 + uCr 2 O 3 , where x, y, z, and u are 25 ≦ x ≦ 80, respectively.
(mol%), 1 ≦ y ≦ 5 (mol%), 10 ≦ z ≦ 70 (mol%), 0.5
A porcelain composition having a composition satisfying <u ≦ 10 (mol%).
Description
【0001】[0001]
【産業上の利用分野】本発明は、MgO−CaO−TiO2
−Cr2O3系からなる磁器組成物に係り、比較的に比誘
電率εrが大きく、高周波帯域における誘電正接 tanδ
が小さく、誘電率の温度係数が組成により−50ないし50
ppm/℃程度の範囲で制御でき、かつ、高周波帯域にお
いて安定に作用する磁器組成物に関する。The present invention relates to MgO-CaO-TiO 2
-Cr 2 O 3 -based porcelain composition has a relatively large relative permittivity ε r and a dielectric loss tangent tan δ in a high frequency band.
Is small and the temperature coefficient of the dielectric constant is -50 to 50 depending on the composition.
The present invention relates to a porcelain composition that can be controlled in the range of ppm / ° C. and that operates stably in a high frequency band.
【0002】[0002]
【従来の技術】近年、マイクロ波に代表される高周波帯
域での周波数共振器(以下、単に共振器と略す)マイクロ
ストリップ用のアンテナ基板などの高周波用部品に、比
較的高誘電率で低損失の誘電体磁器材料が積極的に用い
られ、機器の安定化、小型化が図られている。従来、こ
れらの誘電体磁器材料としては、MgO−CaO−TiO2
系の3成分の磁器組成物やこの3元系に他の添加物を加
えたものが検討されていた。2. Description of the Related Art In recent years, frequency resonators in the high frequency band represented by microwaves (hereinafter simply referred to as "resonators") are used in high frequency components such as antenna substrates for microstrips, and have a relatively high dielectric constant and low loss. The dielectric porcelain material is used positively to stabilize and downsize the equipment. Conventionally, as these dielectric ceramic materials, MgO-CaO-TiO 2
The three-component porcelain composition of the system and the addition of other additives to this ternary system have been investigated.
【0003】[0003]
【発明が解決しようとする課題】しかしながら、MgO
−CaO−TiO2系磁器は誘電率の温度係数及び誘電正
接tanδを共に小さくできる組成範囲が狭く、組成比を
変えると比誘電率εrと、その温度係数が同時に変化す
るため、例えば誘電体磁器の誘電正接 tanδが最小で比
誘電率εrの温度係数が±0ppm/℃附近の値が得られる
ような組成での比誘電率εrは15程度であり、これ以上
の大きな比誘電率εrを得ることが困難であった。[Problems to be Solved by the Invention] However, MgO
-CaO-TiO 2 based ceramic has a narrow composition range which can both reduce the temperature coefficient and dielectric loss tangent tanδ of the dielectric constant, changing the composition ratio and the relative dielectric constant epsilon r, because the temperature coefficient changes at the same time, for example, a dielectric the relative dielectric constant epsilon r of the composition, such as the temperature coefficient of the dielectric constant epsilon r dielectric loss tangent tanδ of the porcelain with a minimum is obtained a value of ± 0 ppm / ° C. vicinity is about 15, more large specific dielectric constant of It was difficult to obtain ε r .
【0004】一方、共振器等の高周波用部品の小型化に
はさらに比誘電率εrの大きな材料が必要であり、その
ためにMgO−CaO−TiO2系にLa2O3,Al2O3等
を添加することが検討されてきた。添加物としてLa2O
3を添加する場合、大気中のCO2と反応するために組成
変動を起こし、量産化,工業化に際して組成の制御が困
難であった。また、Al2O3を添加する場合は、焼結温
度が約1500℃の高温度となり、コスト高となる等の欠点
があった。On the other hand, in order to miniaturize high frequency components such as a resonator, a material having a large relative permittivity ε r is required. Therefore, Mg 2 O 3 Ca 2 O 3 and Al 2 O 3 are added to the MgO—CaO—TiO 2 system. Has been studied. La 2 O as an additive
When 3 is added, composition change occurs due to reaction with CO 2 in the atmosphere, and it was difficult to control the composition during mass production and industrialization. Further, when Al 2 O 3 is added, there is a drawback that the sintering temperature becomes a high temperature of about 1500 ° C. and the cost becomes high.
【0005】本発明は上記従来の問題に鑑み、比誘電率
εrが大きく、高周波帯域での誘電正接 tanδが小さ
く、誘電率の温度係数が組成により制御可能な、かつ、
安定な磁器組成物の提供を目的とする。In view of the above conventional problems, the present invention has a large relative permittivity ε r , a small dielectric loss tangent tan δ in a high frequency band, and a temperature coefficient of the permittivity can be controlled by the composition, and
It is intended to provide a stable porcelain composition.
【0006】[0006]
【課題を解決するための手段】本発明は、成分の組成範
囲をxMgO・yCaO・zTiO2・uCr2O3として表
したときx,y,z,uが、それぞれ、25≦x≦80mol
%,1≦y≦5mol%,10≦z≦70mol%,0<u≦10mo
l%を満足する範囲にあることを特徴とする。Means for Solving the Problems The present invention, x when expressed the composition range of component as xMgO · yCaO · zTiO 2 · uCr 2 O 3, y, z, u , respectively, 25 ≦ x ≦ 80 mol
%, 1 ≦ y ≦ 5 mol%, 10 ≦ z ≦ 70 mol%, 0 <u ≦ 10mo
It is characterized in that it is in a range satisfying l%.
【0007】[0007]
【作用】磁器組成物を構成するMgOが80mol%を超え、
CaOが5mol%を超え、TiO2が70mol%を超えると、
誘電率の温度係数が急激に負へ増大し、組成変動による
特性の変化が大となり、また、MgOが25mol%未満,C
aOが1mol%未満,TiO2が10mol%未満では焼結後の
収縮によって磁器素材にクラックが生じ易く、実用化に
対し困難がある。さらにまた、Cr2O3が10mol%を超え
ると、誘電率の温度係数は急激に負へ増大し、組成変動
による特性の変化が大となり、また誘電正接 tanδが劣
化する。したがって本発明は上記範囲を除いた成分構成
とすることにより、比誘電率εrが比較的大きく、高周
波帯域での誘電正接 tanδが小さく、誘電率の温度係数
が組成により制御でき、かつ、安定な磁器組成物が得ら
れる。[Operation] MgO constituting the porcelain composition exceeds 80 mol%,
When CaO exceeds 5 mol% and TiO 2 exceeds 70 mol%,
The temperature coefficient of the permittivity rapidly increases to a negative value, the characteristics change due to compositional changes, and the MgO content is less than 25 mol%, C
If aO is less than 1 mol% and TiO 2 is less than 10 mol%, the ceramic material tends to crack due to shrinkage after sintering, which is difficult to put into practical use. Furthermore, when Cr 2 O 3 exceeds 10 mol%, the temperature coefficient of the dielectric constant sharply increases to a negative value, the characteristics change largely due to compositional variations, and the dielectric loss tangent tan δ deteriorates. Therefore, according to the present invention, by adopting a composition excluding the above range, the relative permittivity ε r is relatively large, the dielectric loss tangent tan δ in the high frequency band is small, the temperature coefficient of the permittivity can be controlled by the composition, and the stability is stable. A porcelain composition that is easy to obtain is obtained.
【0008】[0008]
【実施例】以下、実施例を説明する。EXAMPLES Examples will be described below.
【0009】まず、原料粉末に純度99.5%以上のMg
O,CaO,TiO2,Cr2O3の各粉末を、表1に示す所
定の組成となるように秤量し、ボール・ミルにより純水
とともに湿式混合した。ついで、前記混合物を乾燥させ
た後空気中において1000℃の温度で2時間仮焼成した。First, the raw material powder contains Mg having a purity of 99.5% or more.
Each powder of O, CaO, TiO 2 , and Cr 2 O 3 was weighed so as to have a predetermined composition shown in Table 1 and wet-mixed with pure water by a ball mill. Then, the mixture was dried and then calcined in air at a temperature of 1000 ° C. for 2 hours.
【0010】[0010]
【表1】 [Table 1]
【0011】上記の仮焼物を再びボール・ミルで湿式粉
砕して平均粒子径を1ないし2μmに形成した後、脱水
乾燥した。The above calcined product was again wet-ground with a ball mill to form an average particle size of 1 to 2 μm, and then dehydrated and dried.
【0012】この粉末に濃度10%のポリビニールアルコ
ール溶液を約7wt%添加して造粉し、60メッシュの篩い
を通して整粒した造粒粉を金型と油圧プレスを用いて10
00kg/cm2の成型圧力が直径15mm,高さ7mmの形状に成型
した。About 7 wt% of a 10% concentration polyvinyl alcohol solution was added to this powder to form a granule, and the granulated powder was sieved through a 60-mesh sieve to obtain 10 particles using a die and a hydraulic press.
Molded into a shape with a molding pressure of 00 kg / cm 2 of 15 mm in diameter and 7 mm in height.
【0013】成型体は、その組成に応じて酸化雰囲気中
で1200ないし1400℃の範囲の温度で2時間保持して焼成
した。The molded body was held in an oxidizing atmosphere at a temperature in the range of 1200 to 1400 ° C. for 2 hours and fired depending on its composition.
【0014】以上のようにした得られた磁器を、所定の
寸法に加工して25℃,8GHzにおける比誘電率εr,誘
電正接 tanδを求めた。The porcelain obtained as described above was processed into predetermined dimensions, and the relative permittivity ε r and the dielectric loss tangent tan δ at 25 ° C. and 8 GHz were determined.
【0015】また、比誘電率の温度係数(Tkppm/℃)
は、−50℃ないし+120℃の温度範囲における静電容量
の変化を共振周波数の変化(Tfppm/℃)として求め、数
1の式からTkを求めた。The temperature coefficient of relative permittivity (T k ppm / ° C.)
Was calculated as a change in resonance frequency (T f ppm / ° C.) in the temperature range of −50 ° C. to + 120 ° C., and T k was calculated from the equation (1).
【0016】[0016]
【数1】 [Equation 1]
【0017】ただし、数1の式でTfは共振周波数の温
度係数、Tkは誘電率の温度係数、α 磁器の熱膨張係数
である。However, in the equation (1), T f is the temperature coefficient of the resonance frequency, T k is the temperature coefficient of the dielectric constant, and α is the thermal expansion coefficient of the porcelain.
【0018】また、この時の測定法は誘電体円柱透過法
を用いた。すなわち、前記のようにして得られた円柱状
の試料を、上下2枚の金属板を用いて挾持させて共振器
を構成し、そのTE011モードから比誘電率εr,誘電正
接 tanδ及び共振周波数の温度係数Tfを求めた。The measuring method used at this time was the dielectric cylinder transmission method. That is, the cylindrical sample obtained as described above is sandwiched between two upper and lower metal plates to form a resonator, and the relative permittivity ε r , the dielectric loss tangent tan δ and the resonance are calculated from the TE 011 mode. The temperature coefficient of frequency T f was determined.
【0019】以上のようにして得られた結果を前出の表
1に示してある。The results obtained as described above are shown in Table 1 above.
【0020】なお、表1において、試料番号5,8,1
0,12,13,16,17の試料は、本発明による限定外の組
成からなる磁器であり、試料番号19,20,21の試料は比
較例であり、上記以外が本発明の実施例の試料である。In Table 1, sample numbers 5, 8, 1
Samples 0, 12, 13, 16, and 17 are porcelains having compositions other than the limits according to the present invention, and samples Nos. 19, 20, and 21 are comparative examples. It is a sample.
【0021】表1に示した試料結果より明らかなよう
に、本発明による磁器組成物は高周波帯域において比誘
電率εrが比較的大きく、誘電正接が小であり、さら
に、その組成によって誘電率の温度係数を制御すること
ができ、かつ、安定であり、工業上のその利用範囲、あ
るいは価値が極めて大きい材料である。As is clear from the sample results shown in Table 1, the porcelain composition according to the present invention has a relatively large relative permittivity ε r and a small dielectric loss tangent in the high frequency band. It is a material that can control the temperature coefficient of, and is stable, and has an extremely large industrial application range or value.
【0022】[0022]
【発明の効果】以上の説明から判るとおり本発明の磁器
組成物は高周波帯域における比誘電率が比較的大きく誘
電正接が小さいので高周波域における電子部品に用いる
誘電体として、すぐれた効果を発揮することができる。As can be seen from the above description, the porcelain composition of the present invention has a relatively large relative dielectric constant in the high frequency band and a small dielectric loss tangent, and therefore exhibits excellent effects as a dielectric used in electronic parts in the high frequency band. be able to.
Claims (1)
ウム(CaO),酸化チタン(TiO2)および、酸化クロム
(Cr2O3)から成る磁器組成物であって、この成分の組
成範囲をxMgO・yCaO・zTiO2・uCr2O3とし
て表したときx,y,z,uが、それぞれ、 25≦ x ≦80 mol% 1≦ y ≦5 mol% 10≦ z ≦70 mol% 0< u ≦10 mol% を満足する範囲にあることを特徴とする磁器組成物。1. Magnesium oxide (MgO), calcium oxide (CaO), titanium oxide (TiO 2 ) and chromium oxide.
A porcelain composition comprising (Cr 2 O 3 ), where x, y, z and u are each 25 ≦ x when the composition range of this component is expressed as xMgO · yCaO · zTiO 2 · uCr 2 O 3. A porcelain composition characterized by being in a range satisfying ≤80 mol% 1 ≤y ≤5 mol% 10 ≤z ≤70 mol% 0 <u ≤10 mol%.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3253689A JPH0597511A (en) | 1991-10-01 | 1991-10-01 | Porcelain composition |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP3253689A JPH0597511A (en) | 1991-10-01 | 1991-10-01 | Porcelain composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JPH0597511A true JPH0597511A (en) | 1993-04-20 |
Family
ID=17254781
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP3253689A Pending JPH0597511A (en) | 1991-10-01 | 1991-10-01 | Porcelain composition |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPH0597511A (en) |
-
1991
- 1991-10-01 JP JP3253689A patent/JPH0597511A/en active Pending
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