JPS5935481B2 - oxide dielectric materials - Google Patents
oxide dielectric materialsInfo
- Publication number
- JPS5935481B2 JPS5935481B2 JP51144242A JP14424276A JPS5935481B2 JP S5935481 B2 JPS5935481 B2 JP S5935481B2 JP 51144242 A JP51144242 A JP 51144242A JP 14424276 A JP14424276 A JP 14424276A JP S5935481 B2 JPS5935481 B2 JP S5935481B2
- Authority
- JP
- Japan
- Prior art keywords
- oxide dielectric
- cao
- pbo
- dielectric material
- zno
- 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.)
- Expired
Links
- 239000003989 dielectric material Substances 0.000 title claims description 14
- 239000000203 mixture Substances 0.000 claims description 10
- ZKATWMILCYLAPD-UHFFFAOYSA-N niobium pentoxide Inorganic materials O=[Nb](=O)O[Nb](=O)=O ZKATWMILCYLAPD-UHFFFAOYSA-N 0.000 description 7
- 239000000463 material Substances 0.000 description 4
- 239000003990 capacitor Substances 0.000 description 2
- 230000007423 decrease Effects 0.000 description 2
- 238000010304 firing Methods 0.000 description 2
- 229910017676 MgTiO3 Inorganic materials 0.000 description 1
- 229910019704 Nb2O Inorganic materials 0.000 description 1
- PNEYBMLMFCGWSK-UHFFFAOYSA-N aluminium oxide Inorganic materials [O-2].[O-2].[O-2].[Al+3].[Al+3] PNEYBMLMFCGWSK-UHFFFAOYSA-N 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 230000006835 compression Effects 0.000 description 1
- 238000007906 compression Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 230000002093 peripheral effect Effects 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000035939 shock Effects 0.000 description 1
- 239000000758 substrate Substances 0.000 description 1
Landscapes
- Compositions Of Oxide Ceramics (AREA)
- Ceramic Capacitors (AREA)
- Inorganic Insulating Materials (AREA)
Description
【発明の詳細な説明】
本発明は、Ca、Zn、Pb、Nbを主要成分とする酸
化物誘電材料に関するものである。DETAILED DESCRIPTION OF THE INVENTION The present invention relates to an oxide dielectric material containing Ca, Zn, Pb, and Nb as main components.
本発明の目的は、誘電率(ε)が17以上で誘電体損失
(tanδ)が小さく且つ誘電率温度係数(εT、にと
記す)を正または負の任意の値に制御可能なマイクロ波
誘電材料およびコンデンサ材料に適した酸化物誘電材料
を提供することである。誘電材料は、従来からマイクロ
波回路のインピーダンスの整合、誘電体共振器等に広く
応用されてきた。The purpose of the present invention is to provide a microwave dielectric material having a dielectric constant (ε) of 17 or more, a small dielectric loss (tan δ), and a temperature coefficient of dielectric constant (εT) that can be controlled to any positive or negative value. An object of the present invention is to provide an oxide dielectric material suitable for materials and capacitor materials. Dielectric materials have been widely applied to impedance matching in microwave circuits, dielectric resonators, and the like.
この傾向はますます促進され、近来では、通信網の増加
に伴い使用周波数領域も低周波領域、準ミリ波領域、ミ
リ波領域と広がり、マイクロ波IC化の要請とともにそ
の周辺技術が進歩したことと相俟つて発振器の周波数の
安定化、遅延時間の制御、およびマイクロ波回路用工C
基板等にも、高誘電率低損失の誘電材料を使うことが積
極的に検討されている。従来の一般的な誘電材料として
はBaO−jTi02系のものが知られているが、誘電
率温度係数εT、には負の大きい値を示し、正の値は得
られない。This trend has been further accelerated, and in recent years, with the increase in communication networks, the frequency range used has expanded to the low frequency range, quasi-millimeter wave range, and millimeter wave range, and with the demand for microwave ICs, peripheral technologies have advanced. In conjunction with this, it is possible to stabilize the oscillator frequency, control the delay time, and improve microwave circuit engineering.
Active consideration is being given to using dielectric materials with high dielectric constant and low loss for substrates and the like. BaO-jTi02-based materials are known as conventional general dielectric materials, but the dielectric constant temperature coefficient εT exhibits a large negative value and a positive value cannot be obtained.
また、アルミナ焼結体、MgTiO3系、CaTi03
系等では、正の値こそ他の条件も満たしたまま得られる
が、正から負に亘る値を得ようとすれば一δが大きくな
る欠点があつた。本発明はこれらの欠点を除いたもので
あり、CaO−ZnO−PbO−Nb2O5の4成分系
で酸化物誘電体を構成することにより、問題の誘電率温
度係数を正から負に亘る広い範囲で任意にコントロール
し得るマイクロ用、コンデンサ用、温度補償用等に優れ
た特性を発揮する高誘電率低損失の優れた誘電体を提供
する。更に、本発明によるCaO−ZnO−PbO一N
b2O5の4成分系からなる酸化物誘電材料において、
(CaO)a(ZnO)b(PbO)c(Nb2O5)
dとあられしたときに、各成分系の組成比a、b、c、
d(7)総和が1であり、各々の組成比が0.050≦
a≦0.450、0.10≦を≦0.60、0.0≦c
≦0.035、残りdの条件を満l 足するようにした
ものは、特に優秀な特性を示す。In addition, alumina sintered body, MgTiO3 system, CaTi03
In systems, positive values can be obtained while other conditions are satisfied, but if you try to obtain values ranging from positive to negative, δ becomes large. The present invention eliminates these drawbacks, and by constructing an oxide dielectric with a four-component system of CaO-ZnO-PbO-Nb2O5, the temperature coefficient of permittivity can be changed over a wide range from positive to negative. To provide an excellent dielectric material with high dielectric constant and low loss that exhibits excellent characteristics for micro devices, capacitor devices, temperature compensation devices, etc. that can be controlled arbitrarily. Furthermore, CaO-ZnO-PbO-N according to the present invention
In an oxide dielectric material consisting of a four-component system of b2O5,
(CaO)a(ZnO)b(PbO)c(Nb2O5)
When hail d occurs, the composition ratios of each component system are a, b, c,
d(7) The total sum is 1, and each composition ratio is 0.050≦
a≦0.450, 0.10≦≦0.60, 0.0≦c
≦0.035 and the remaining d satisfies the conditions, and exhibits particularly excellent characteristics.
以下、本発明を実施の一例を挙げて詳細に説明する。個
々の実施例についてのデータは、CaO、ZnO、Pb
O、Nb2O5各々の原料を各組成に・ 応じて秤量し
、ボールミルにて混合し、濾過乾燥後1000℃の温度
下で4時間仮焼し、圧縮成形後、1160〜1250℃
の温度下で2時間大気中もしくは酸素雰囲気中で焼成を
行なつて得た試料で測定したものである。Hereinafter, the present invention will be explained in detail by giving an example of implementation. Data for individual examples include CaO, ZnO, Pb
The raw materials for O and Nb2O5 are weighed according to their respective compositions, mixed in a ball mill, filtered and dried, then calcined for 4 hours at a temperature of 1000°C, and after compression molded at a temperature of 1160 to 1250°C.
This was measured using a sample obtained by firing at a temperature of 2 hours in the air or oxygen atmosphere.
誘電率の常温測定、誘電率の温度係数等はIMHzから
Xバンドのマイクロ波帯域にかけて測定した。本発明を
実施した酸化物誘電材料の組成を(CaO)a(ZnO
)b(PbO)c(Nb2O5)dと表記したとき、a
+b+c+d=1.00となるようにしつつそれぞれA
,b,c,dの値をかえた場合について、Xバンド周波
数(6GHz)で測定した諸特性を第1表に示す。The dielectric constant was measured at room temperature, the temperature coefficient of the dielectric constant, etc. were measured in the microwave band from IMHz to the X band. The composition of the oxide dielectric material in which the present invention is implemented is (CaO)a(ZnO
) b (PbO) c (Nb2O5) d, when a
+b+c+d=1.00 while each A
, b, c, and d, various characteristics measured at the X-band frequency (6 GHz) are shown in Table 1.
第1表に示すごとくCaO/ZnO/PbO/Nb2O
5の組成比を変えた場合、PbOすなわちCの値が多く
なるにしたがい誘電率の温度係数εT.Kは小さくなり
、C=0.0164〜0.0323の組成の間で+35
P/℃から−101P/℃という小さな直を示す。As shown in Table 1, CaO/ZnO/PbO/Nb2O
5, the temperature coefficient of dielectric constant εT. K becomes smaller and +35 between compositions of C=0.0164 and 0.0323.
It shows a small change from P/℃ to -101P/℃.
特にa=0.129,b=0.5161,c=0.03
23,d=0.3226の組成では−2±2P/℃とい
う小さな値を示す。Cの値が多くなるに伴い正から負の
εT.Kを示し、c〉0.045ではεT.Kは負にな
り、Q(Q=1/Tanδ)が大幅に低下する。このた
めc〉0.045ではA,b,dのどんな組合せの組成
においても同様の傾向となるため、本発明から除外する
。a≦0.04,a≧0.50,.b≦0.052,b
≧0.65、C>0.045,d≦0.29,d≧0.
60の範囲の組合せによる組成比では、Qの低下に加え
εT.Kが大きくなるため実用的に好ましくない。また
この範囲では焼結体が熱シヨツクに弱くなり亀裂が入り
易くなる。以上のごとく、A,b,c,dの値を適宜に
選.ぶことで、高いQを保持しながら任意に正、負のε
T.Kの値を得ることが可能である。Especially a=0.129, b=0.5161, c=0.03
23, the composition of d=0.3226 shows a small value of -2±2P/°C. As the value of C increases, εT. K, and for c>0.045, εT. K becomes negative and Q (Q=1/Tanδ) decreases significantly. Therefore, when c>0.045, the same tendency occurs regardless of the composition of any combination of A, b, and d, and this is excluded from the present invention. a≦0.04, a≧0.50, . b≦0.052, b
≧0.65, C>0.045, d≦0.29, d≧0.
With a combination of composition ratios in the range of 60, in addition to a decrease in Q, εT. Since K becomes large, this is not practically preferable. In addition, within this range, the sintered body becomes susceptible to thermal shock and cracks are likely to occur. As mentioned above, the values of A, b, c, and d are selected appropriately. By holding high Q, we can arbitrarily set positive or negative ε.
T. It is possible to obtain the value of K.
一方焼成温度も1160〜1250℃と比較的低温度で
焼結体を得ることができ経済的である。このように本発
明による酸化物誘電材料は、誘電率の低いところで誘電
体損失が極めて小さく、且つ誘電率の温度係数が小さく
又正、負の任意の値を得ることができる優れた材料であ
ることがわかる。On the other hand, the sintered body can be obtained at a relatively low firing temperature of 1160 to 1250°C, which is economical. As described above, the oxide dielectric material according to the present invention is an excellent material that has extremely small dielectric loss at a low dielectric constant, has a small temperature coefficient of dielectric constant, and can obtain any positive or negative value. I understand that.
Claims (1)
系かならる酸化物誘電材料。 2 CaO−ZnO−PbO−Nb_2O_5の4成分
系からなる酸化物誘電材料において、(CaO)a(Z
nO)b(PbO)c(Nb_2O_5)dとあらわし
たときに、各成分系の組成比a、b、c、dの総和が1
であり、各々の組成比が0.050≦a≦0.450、
0.10≦b≦0.60、0.0≦c≦0.035、残
りdの条件を満すようにした前記第1項記載の酸化物誘
電材料。[Claims] 1. An oxide dielectric material consisting of a four-component system of CaO-ZnO-PbO-Nb_2O_5. 2 In an oxide dielectric material consisting of a four-component system of CaO-ZnO-PbO-Nb_2O_5, (CaO)a(Z
When expressed as nO)b(PbO)c(Nb_2O_5)d, the sum of the composition ratios a, b, c, and d of each component system is 1.
and each composition ratio is 0.050≦a≦0.450,
The oxide dielectric material according to item 1, which satisfies the following conditions: 0.10≦b≦0.60, 0.0≦c≦0.035, and the remainder d.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51144242A JPS5935481B2 (en) | 1976-11-30 | 1976-11-30 | oxide dielectric materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP51144242A JPS5935481B2 (en) | 1976-11-30 | 1976-11-30 | oxide dielectric materials |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS5368897A JPS5368897A (en) | 1978-06-19 |
| JPS5935481B2 true JPS5935481B2 (en) | 1984-08-29 |
Family
ID=15357538
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP51144242A Expired JPS5935481B2 (en) | 1976-11-30 | 1976-11-30 | oxide dielectric materials |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS5935481B2 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS58135508A (en) * | 1982-02-05 | 1983-08-12 | 日本電気株式会社 | Oxide dielectric material |
-
1976
- 1976-11-30 JP JP51144242A patent/JPS5935481B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JPS5368897A (en) | 1978-06-19 |
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