JP2000335967A - Piezoelectric ceramic composition - Google Patents
Piezoelectric ceramic compositionInfo
- Publication number
- JP2000335967A JP2000335967A JP11150054A JP15005499A JP2000335967A JP 2000335967 A JP2000335967 A JP 2000335967A JP 11150054 A JP11150054 A JP 11150054A JP 15005499 A JP15005499 A JP 15005499A JP 2000335967 A JP2000335967 A JP 2000335967A
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- JP
- Japan
- Prior art keywords
- composition
- piezoelectric ceramic
- ceramic composition
- general formula
- based component
- 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.)
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Abstract
Description
【0001】[0001]
【発明の属する技術分野】本発明は、波動デバイス、フ
ィルター、共振子等に用いられる圧電磁器組成物に関す
る。The present invention relates to a piezoelectric ceramic composition used for a wave device, a filter, a resonator, and the like.
【0002】[0002]
【従来の技術】従来、この種の圧電磁器組成物として
は、二成分で構成されるPZT(PbTiO3−PbZ
rO3)系磁器や三成分で構成されるPCM[PbTi
O3−PbZrO3−Pb(Mg0.5Nb0.5)T
iO3]系磁器が主に用いられてきた。その理由として
は、上記の組成物が大きな圧電性を示すことはもちろん
であるが、それとともに、その用途がセンサー、アクチ
ュエーター、フィルター等多種にわたり、各用途に要求
される特性も様々であるのに対し、上記組成系では、各
成分量の割合を調整することにより、要求に対応した特
性に適宜に操作できるからである。2. Description of the Related Art Conventionally, as a piezoelectric ceramic composition of this kind, PZT (PbTiO 3 -PbZ) composed of two components has been used.
rO 3 ) -based porcelain or PCM [PbTi
O 3 -PbZrO 3 -Pb (Mg 0.5 Nb 0.5) T
iO 3 ] -based porcelain has been mainly used. The reason for this is, of course, that the above-mentioned composition exhibits large piezoelectricity, but at the same time, its applications are various, such as sensors, actuators and filters, and the characteristics required for each application are also various. On the other hand, in the above composition system, by adjusting the ratio of the amounts of the respective components, it is possible to appropriately operate to the characteristics corresponding to the requirements.
【0003】しかし、これらの組成物は、いずれも鉛を
主成分とするもので、原料比で酸化鉛として60wt%
以上も含まれている。酸化鉛は、低温でも揮発性が高
く、仮焼、焼結等の製造時に揮発したり、また、産業廃
棄物中から溶出することも考えられる。しかし、この対
策をするには、設備設置のため膨大な費用を投じなけれ
ばならない。そこで、無鉛で、大きな圧電特性を示す材
料が要望されている。However, each of these compositions contains lead as a main component and has a raw material ratio of 60 wt% as lead oxide.
The above is also included. Lead oxide has high volatility even at low temperatures, and may be volatilized during production such as calcination or sintering, or may be eluted from industrial waste. However, this measure requires enormous costs for installation of the equipment. Therefore, there is a demand for a material that is lead-free and that exhibits large piezoelectric characteristics.
【0004】また、既存の無鉛圧電磁器組成物、一般式
(Bi0.5Na0.5)TiO3は、機械的品質係数
Qmの値が低く、高いQmが必要とされるフィルター、
共振子等の用途に適用することは困難であった。An existing lead-free piezoelectric ceramic composition, a general formula (Bi 0.5 Na 0.5 ) TiO 3 , has a low mechanical quality factor Qm and a filter that requires a high Qm.
It has been difficult to apply it to applications such as resonators.
【0005】[0005]
【発明が解決しようとする課題】本発明は、上記の課題
を解決し、無鉛で、高いQmを有する圧電磁器組成物を
提供することにある。An object of the present invention is to solve the above-mentioned problems and to provide a lead-free piezoelectric ceramic composition having a high Qm.
【0006】[0006]
【課題を解決するための手段】本発明は、一般式(1−
X)(Bi0.5Na0.5)TiO3−XBiCrO
3で表され、Xが0.03≦X≦0.3の範囲であるこ
とを特徴とする圧電磁器組成物である。According to the present invention, there is provided a compound represented by the general formula (1-
X) (Bi 0.5 Na 0.5) TiO 3 -XBiCrO
3. A piezoelectric ceramic composition represented by formula 3 , wherein X is in the range of 0.03 ≦ X ≦ 0.3.
【0007】[0007]
【発明の実施の形態】主成分原料として、化学的に高純
度であるBi2O3、Na2CO3、TiO 2、Cr2
O3を用いた。これらを一般式(1−X)(Bi0.5
Na0.5)TiO3−XBiCrO3(0≦X≦0.
4)に対し化学量論的に配合し、ボールミルによりエタ
ノール中で20時間混合した。これを800℃で1時間
保持して仮焼し、次に、10時間粉砕を行った。バイン
ダーとしてポリビニルアルコールを用い造粒し、圧力1
ton/cm2で直径20mm、厚さ1mmの円板状に
加圧成形した。焼成は、温度1050〜1150℃で2
時間保持して行った。DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
Bi that is a degree2O3, Na2CO3, TiO 2, Cr2
O3Was used. These are represented by the general formula (1-X) (Bi0.5
Na0.5) TiO3-XBiCrO3(0 ≦ X ≦ 0.
4) is stoichiometrically compounded, and is
Mix in knoll for 20 hours. One hour at 800 ° C
It was calcined while holding, and then pulverized for 10 hours. Vine
Granulation using polyvinyl alcohol as the
ton / cm2Into a disc with a diameter of 20mm and a thickness of 1mm
It was molded under pressure. The firing is performed at a temperature of 1050 to 1150 ° C for 2 hours.
It was held for a while.
【0008】この焼結体の両面に銀電極を設け、100
℃のシリコーンオイル中で直流電圧4kV/mmを電極
間に加え、焼結体を厚み方向に分極した。A silver electrode is provided on both sides of the sintered body,
A direct current voltage of 4 kV / mm was applied between the electrodes in silicone oil at ℃ to polarize the sintered body in the thickness direction.
【0009】そして、これらの試料について圧電、誘電
特性の測定を行った。圧電特性は、LFインピーダンス
アナライザーを用い、共振−反共振法により電気機械結
合係数k33、kp、kt、機械的品質係数Qmを算出
し、評価した。また、誘電特性は、LCRメータを用い
て周波数1MHzで測定を行い、比誘電率ε33 t/ε
0で評価した。Then, the piezoelectric and dielectric properties of these samples were measured. The piezoelectric characteristics, using a LF impedance analyzer, resonant - electromechanical coupling coefficient k 33, kp, kt, the mechanical quality factor Qm was calculated by antiresonance method, and evaluated. The dielectric properties were measured at a frequency of 1 MHz using an LCR meter, and the relative permittivity ε 33 t / ε was measured.
It was rated 0 .
【0010】表1に、(1−X)(Bi0.5Na
0.5)TiO3−XBiCrO3において、0≦X≦
0.4の範囲におけるk33、kp、kt、Qm、及び
ε33 t/ε0を示す。Table 1 shows that (1-X) (Bi 0.5 Na
0.5 ) In TiO 3 —XBiCrO 3 , 0 ≦ X ≦
Show k 33 , kp, kt, Qm and ε 33 t / ε 0 in the range of 0.4.
【0011】[0011]
【表1】 [Table 1]
【0012】表1において、Qmは、X=0.2で、最
大値1288であり、(Bi0.5Na0.5)TiO
3に対し、Qmが顕著に改善していることが確認でき
た。しかし、0.03≦X≦0.3の範囲外では、Qm
が700以下と非常に小さく、実用化は難しいことがわ
かった。In Table 1, Qm has a maximum value of 1288 when X = 0.2, and (Bi 0.5 Na 0.5 ) TiO
In contrast to 3 , it was confirmed that Qm was significantly improved. However, outside the range of 0.03 ≦ X ≦ 0.3, Qm
Was very small at 700 or less, which proved difficult to put into practical use.
【0013】また、0.03≦X≦0.3の範囲では、
k33、kp、ktも増加しており、実用に適している
ことがわかった。In the range of 0.03 ≦ X ≦ 0.3,
The values of k 33 , kp, and kt also increased, indicating that they were suitable for practical use.
【0014】以上より、(Bi0.5Na0.5)Ti
O3にBiCrO3を3〜30mol%固溶させること
により、(Bi0.5Na0.5)TiO3のk33、
kp、ktを劣化させることなく、Qmを向上させるこ
とができる。これにより、フィルター、共振子等の用途
への適用が可能となる。From the above, (Bi 0.5 Na 0.5 ) Ti
By dissolving 3 to 30 mol% of BiCrO 3 in O 3 , k 33 of (Bi 0.5 Na 0.5 ) TiO 3 ,
Qm can be improved without deteriorating kp and kt. This enables application to applications such as filters and resonators.
【0015】[0015]
【発明の効果】以上説明したように、本発明によれば、
無鉛で、高いQmを有する圧電磁器組成物を提供するこ
とができた。As described above, according to the present invention,
A lead-free piezoelectric ceramic composition having a high Qm could be provided.
Claims (1)
0.5)TiO3−XBiCrO3で表され、Xが0.
03≦X≦0.3の範囲であることを特徴とする圧電磁
器組成物。1. A compound of the formula (1-X) (Bi 0.5 Na
0.5) is represented by TiO 3 -XBiCrO 3, X is 0.
A piezoelectric ceramic composition characterized by satisfying the following condition: 03 ≦ X ≦ 0.3.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15005499A JP4141051B2 (en) | 1999-05-28 | 1999-05-28 | Piezoelectric ceramic composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP15005499A JP4141051B2 (en) | 1999-05-28 | 1999-05-28 | Piezoelectric ceramic composition |
Publications (2)
Publication Number | Publication Date |
---|---|
JP2000335967A true JP2000335967A (en) | 2000-12-05 |
JP4141051B2 JP4141051B2 (en) | 2008-08-27 |
Family
ID=15488509
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP15005499A Expired - Lifetime JP4141051B2 (en) | 1999-05-28 | 1999-05-28 | Piezoelectric ceramic composition |
Country Status (1)
Country | Link |
---|---|
JP (1) | JP4141051B2 (en) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013179260A (en) * | 2012-01-31 | 2013-09-09 | Tdk Corp | Piezoelectric composition and piezoelectric element |
JP2014209554A (en) * | 2013-03-29 | 2014-11-06 | Tdk株式会社 | Piezoelectric composition and piezoelectric device |
CN113198458A (en) * | 2021-04-21 | 2021-08-03 | 中国海洋大学 | Bismuth-chromium composite oxide semiconductor photocatalyst and preparation method and application thereof |
-
1999
- 1999-05-28 JP JP15005499A patent/JP4141051B2/en not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2013179260A (en) * | 2012-01-31 | 2013-09-09 | Tdk Corp | Piezoelectric composition and piezoelectric element |
JP2014209554A (en) * | 2013-03-29 | 2014-11-06 | Tdk株式会社 | Piezoelectric composition and piezoelectric device |
CN113198458A (en) * | 2021-04-21 | 2021-08-03 | 中国海洋大学 | Bismuth-chromium composite oxide semiconductor photocatalyst and preparation method and application thereof |
Also Published As
Publication number | Publication date |
---|---|
JP4141051B2 (en) | 2008-08-27 |
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