JP2003201171A - Piezoelectric porcelain composition - Google Patents

Piezoelectric porcelain composition

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Publication number
JP2003201171A
JP2003201171A JP2001399587A JP2001399587A JP2003201171A JP 2003201171 A JP2003201171 A JP 2003201171A JP 2001399587 A JP2001399587 A JP 2001399587A JP 2001399587 A JP2001399587 A JP 2001399587A JP 2003201171 A JP2003201171 A JP 2003201171A
Authority
JP
Japan
Prior art keywords
piezoelectric
porcelain composition
composition
piezoelectric porcelain
lead
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Withdrawn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
JP2001399587A
Other languages
Japanese (ja)
Inventor
Yasuki Takashima
康樹 鷹島
Hiroyuki Yoshida
弘幸 吉田
Yoichi Mamiya
洋一 間宮
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.)
Tokin Corp
Original Assignee
NEC Tokin 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 NEC Tokin Corp filed Critical NEC Tokin Corp
Priority to JP2001399587A priority Critical patent/JP2003201171A/en
Publication of JP2003201171A publication Critical patent/JP2003201171A/en
Withdrawn legal-status Critical Current

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Abstract

<P>PROBLEM TO BE SOLVED: To provide a piezoelectric porcelain composition having excellent piezoelectric characteristics by using an inexpensive material not containing a lead component. <P>SOLUTION: The piezoelectric porcelain composition is expressed by the chemical formula [Bi<SB>a</SB>(Na<SB>1-x</SB>K<SB>x</SB>)<SB>1-a</SB>]<SB>b</SB>[Ti<SB>1-y</SB>(Mg<SB>c</SB>Ta<SB>1-c</SB>)<SB>y</SB>]<SB>b</SB>O<SB>3</SB>, in which x and y are 0<x<1, 0<y≤0.3. <P>COPYRIGHT: (C)2003,JPO

Description

【発明の詳細な説明】 【0001】 【発明の属する技術分野】本発明は、振動子、アクチュ
エータ、センサ等の圧電デバイスに好適に使用される圧
電磁器組成物に関する。 【0002】 【従来の技術】従来、圧電デバイスに用いられるセラミ
ックス材料は、PT(PbTiO3)あるいはPZT
(Pb(Ti,Zr)O3)に代表されるように鉛を含有
するものがほとんどである。 【0003】 【発明が解決しようとする課題】しかし、これらの鉛を
含有するセラミックスは、製造プロセスにおいて鉛成分
の揮発を免れ得ない。また、産業廃棄物中にこれらの鉛
を含有するセラミックスが含まれている場合、焼却灰や
溶出による環境汚染が考えられる。そのため、鉛成分を
外部環境に排出させない対策が必要となり、膨大なコス
トが発生する。 【0004】これらのことから、無鉛圧電材料を供する
ことは環境対策と同時に製造コストの面からも極めて有
用である。 【0005】ところが、これまでに得られている無鉛圧
電材料においては、圧電特性、あるいは誘電特性などに
おいて、必ずしも実用的に十分ではない。 【0006】そこで、本発明は、鉛成分を含有しない安
価な材料で、優れた圧電特性を有する圧電磁器組成物を
提供することを課題としている。 【0007】 【課題を解決するための手段】上記課題を解決するため
に、本発明の圧電磁器組成物は、Bi(Na1-x )
1-aTi1-y(MgTa1-c)3の化学式で表さ
れ、x,yがモル比で、0<x<1、0<y≦0.3と
することで、鉛を含有しない優れた圧電磁器組成物とな
る。 【0008】 【作用】本発明は、Bi-Na-Ti系圧電材料におい
て、Naの一部をKで置換し、さらにTiの一部をMg
1/3Ta2/3で置換することにより、圧電特性および誘電
特性を改善するものである。 【0009】それぞれの置換量を0<x<1、0<y≦
0.3としたのは、この範囲以外では圧電特性が低下す
るためである。この理由は、詳細には不明であるが、M
PB(モルホトロピック相境界)近傍の組成範囲から大
きく外れることが原因と思われる。 【0010】ところで、本発明の圧電磁器組成物におい
ては、ストイキオメトリー(化学量論比)から少しずれ
た結晶においても優れた圧電特性が得られる。その原因
としては、異相の析出、別サイトとの構成元素の置換、
粒界部への析出、酸素欠陥、あるいは構成元素の価数の
変化などが挙げられる。 【0011】そのときの組成比のずれは、±5%程度ま
で可能である。即ち、本発明の圧電磁器組成物の組成
を、前記x,yの他に、a,b,cおよびdを加えて、
[Bi (Na1-x1-a[Ti1-y(Mg
Ta1-c3のように表したとき、aの値とし
ては、0.5を中心に±5%程度、bの値としては1.0
0を中心に±5%程度、cの値としては1/3を中心に
±5%程度、さらにdの値としては1.00を中心に±
5%程度までの変化が可能である。 【0012】また、セラミックスの製造方法としては、
一般的な製造方法であればよく、特に限定するものでは
ない。 【0013】 【実施例】次に、実施例によって本発明を説明する。 【0014】発明品として、化学的に高純度のBi
23、Na2CO3、K2CO3,TiO2,MgO,Ta2
5を用い、Bi0.5(Na1-x)0.5Ti1-y(Mg
1/3Ta2/ 3)3、(0<x<1,0<y≦0.3)の組
成となるように配合し、アルコールを用いてボールミル
で40時間混合した。 【0015】これを乾燥し、大気中で900℃で1時間
仮焼した。次に、ボールミルで20時間湿式混合を行っ
た。乾燥して得られた粉末をポリビニルアルコールをバ
インダーとして造粒し、圧力1.5トン/cm2の一軸加
圧成形により、直径20mm、厚さ1mmの円板状に成
形した。 【0016】焼成は、l000〜1200℃で2時間行
った。得られた焼結体の上下面を平行研磨し、研磨面に
銀電極を塗布、焼き付けし、l00℃のシリコーンオイ
ル中で4〜7kV/mmの直流電流を15分問印加し、
厚み方向に分極した。 【0017】また、比較品として発明品と同様の製造方
法で組成が請求項に記載の範囲外のものを作製した。 【0018】表1に、発明品と比較品の電気機械結合係
数kpおよびkt、機械的品質係数Qm、比誘電率ε33
を示す。特性は、インピーダンスアナライザー
を用い共振-反共振法により算出した。Naの一部を
K、Tiの一部を(Mg1/3Ta2/ 3)で請求項に記載の
範囲内において置換した発明品は、圧電特性、誘電特性
が改善されている。 【0019】 【表1】【0020】 【発明の効果】以上述べたように、本発明によれば、B
0.5(Na1-x0.5Ti1-y(Mg1/3Ta2/3
3の化学式で表され、x,yがモル比で、0<x<
1、0<y≦0.3とすることで、鉛を含有せず優れた
特性の圧電磁器組成物を得ることが出来る。
DETAILED DESCRIPTION OF THE INVENTION [0001] TECHNICAL FIELD The present invention relates to a vibrator, an actuator,
Pressure suitable for piezoelectric devices such as etas and sensors
It relates to a porcelain composition. [0002] 2. Description of the Related Art Ceramics conventionally used for piezoelectric devices
Material is PT (PbTiOThree) Or PZT
(Pb (Ti, Zr) OThreeContains lead as typified by
Most do. [0003] However, these leads are
The contained ceramic is a lead component in the manufacturing process
The volatilization of is inevitable. In addition, these lead in industrial waste
Ash or ash
Environmental pollution due to elution is possible. Therefore, lead component
Measures that do not release to the external environment are required,
Occurs. For these reasons, lead-free piezoelectric materials are provided.
This is extremely beneficial not only in terms of environmental measures but also in terms of manufacturing costs.
It is for. However, the lead-free pressure obtained so far
In electrical materials, piezoelectric properties or dielectric properties
However, it is not always practically sufficient. [0006] Accordingly, the present invention provides a safety device containing no lead component.
Piezoelectric ceramic compositions with excellent piezoelectric properties
The task is to provide. [0007] [MEANS FOR SOLVING THE PROBLEMS]
The piezoelectric ceramic composition of the present invention isa(Na1-xK x)
1-aTi1-y(MgcTa1-c)yOThreeRepresented by the chemical formula
Where x and y are molar ratios, 0 <x <1, 0 <y ≦ 0.3.
By doing so, it becomes an excellent piezoelectric ceramic composition that does not contain lead.
You. [0008] The present invention relates to a Bi—Na—Ti based piezoelectric material.
Then, part of Na is replaced with K, and part of Ti is further replaced with Mg.
1/3Ta2/3Substitution with piezoelectric properties and dielectric
This is to improve the characteristics. [0009] The respective replacement amounts are 0 <x <1, 0 <y ≦
The reason for setting the ratio to 0.3 is that the piezoelectric characteristics are deteriorated outside this range.
That's because. The reason for this is unknown, but M
Greater than the composition range near PB (morphotropic phase boundary)
The cause seems to be that it comes off easily. [0010] By the way, in the piezoelectric ceramic composition of the present invention,
Is slightly different from stoichiometry (stoichiometric ratio)
Excellent piezoelectric properties can be obtained even for crystals that have been grown. The cause
As the precipitation of a different phase, the replacement of constituent elements with another site,
Precipitation at grain boundaries, oxygen vacancies, or valence of constituent elements
Change and the like. The deviation of the composition ratio at that time is about ± 5%.
Is possible. That is, the composition of the piezoelectric ceramic composition of the present invention
By adding a, b, c and d in addition to the above x and y,
[Bi a(Na1-xKx)1-a]b[Ti1-y(Mgc
Ta1-c)y]dOThreeWhere a is the value of a
About ± 5% around 0.5, and the value of b is 1.0
Approximately ± 5% around 0, and the value of c around 1/3
About ± 5%, and as the value of d, around ± 1.00
Changes up to about 5% are possible. Further, as a method for producing ceramics,
Any production method may be used.
Absent. [0013] Next, the present invention will be described by way of examples. [0014] As an invention, a chemically pure Bi
TwoOThree, NaTwoCOThree, KTwoCOThree, TiOTwo, MgO, TaTwo
OFiveAnd Bi0.5(Na1-xKx)0.5Ti1-y(Mg
1/3Ta2 / Three)yOThree, (0 <x <1, 0 <y ≦ 0.3)
And a ball mill using alcohol.
For 40 hours. [0015] This is dried, at 900 ° C for 1 hour in the air
Calcined. Next, wet mixing was performed for 20 hours using a ball mill.
Was. The powder obtained by drying is coated with polyvinyl alcohol.
Granulated as an inder, pressure 1.5 ton / cmTwoUniaxial addition
Formed into a disc with a diameter of 20 mm and a thickness of 1 mm by pressing.
Shaped. The firing is performed at 1,000 to 1200 ° C. for 2 hours.
Was. The upper and lower surfaces of the obtained sintered body are polished in parallel, and
A silver electrode is applied and baked.
Apply a direct current of 4-7 kV / mm for 15 minutes in the
Polarized in the thickness direction. Also, as a comparative product, the same manufacturing method as the invention product is used.
A composition having a composition outside the range described in the claims was produced by the method. Table 1 shows the electromechanical coupling between the invention product and the comparison product.
Several kp and kt, mechanical quality factor Qm, relative permittivity ε33
T/ εoIs shown. Characteristics are impedance analyzer
Was calculated by the resonance-anti-resonance method. Part of Na
Part of K and Ti (Mg1/3Ta2 / Three) In the claim
The inventions substituted within the range have piezoelectric and dielectric properties.
Has been improved. [0019] [Table 1][0020] As described above, according to the present invention, B
i0.5(Na1-xKx)0.5Ti1-y(Mg1/3Ta2/3)
yOThreeWhere x and y are molar ratios and 0 <x <
1, 0 <y ≦ 0.3, excellent lead-free content
A piezoelectric ceramic composition having characteristics can be obtained.

Claims (1)

【特許請求の範囲】 【請求項1】 Bi0.5(Na1-x)0.5Ti1-y(M
1/3Ta2/3)3の化学式で表され、x,yがモル比
で0<x<1、0<y≦0.3であることを特徴とする
圧電磁器組成物。
Claims: 1. Bi 0.5 (Na 1 -x K x ) 0.5 Ti 1 -y (M
g 1/3 Ta 2/3) represented by the chemical formula of y O 3, x, piezoelectric ceramic composition characterized by y is 0 <x <1,0 <y ≦ 0.3 in molar ratio.
JP2001399587A 2001-12-28 2001-12-28 Piezoelectric porcelain composition Withdrawn JP2003201171A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2001399587A JP2003201171A (en) 2001-12-28 2001-12-28 Piezoelectric porcelain composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001399587A JP2003201171A (en) 2001-12-28 2001-12-28 Piezoelectric porcelain composition

Publications (1)

Publication Number Publication Date
JP2003201171A true JP2003201171A (en) 2003-07-15

Family

ID=27639734

Family Applications (1)

Application Number Title Priority Date Filing Date
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Country Status (1)

Country Link
JP (1) JP2003201171A (en)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005082422A (en) * 2003-09-05 2005-03-31 Tdk Corp Piezoelectric ceramic
JP2007204337A (en) * 2006-02-03 2007-08-16 Seiko Epson Corp Piezoelectric material
JP2008239482A (en) * 2008-04-25 2008-10-09 Taiyo Yuden Co Ltd Piezoelectric ceramic composition, method for producing piezoelectric ceramic composition and piezoelectric ceramic component
JP2008263158A (en) * 2006-09-15 2008-10-30 Canon Inc Piezoelectric element, and liquid discharge head
WO2012044313A1 (en) * 2010-09-30 2012-04-05 Hewlett-Packard Development Company, L.P. Lead-free piezoelectric materials with enhanced fatigue resistance
JP2016115752A (en) * 2014-12-12 2016-06-23 Tdk株式会社 Piezoelectric composition and piezoelectric element

Cited By (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005082422A (en) * 2003-09-05 2005-03-31 Tdk Corp Piezoelectric ceramic
JP4636222B2 (en) * 2003-09-05 2011-02-23 Tdk株式会社 Piezoelectric ceramic
JP2007204337A (en) * 2006-02-03 2007-08-16 Seiko Epson Corp Piezoelectric material
JP4702552B2 (en) * 2006-02-03 2011-06-15 セイコーエプソン株式会社 Piezoelectric element, liquid ejecting head, and liquid ejecting apparatus
JP2008263158A (en) * 2006-09-15 2008-10-30 Canon Inc Piezoelectric element, and liquid discharge head
JP2008239482A (en) * 2008-04-25 2008-10-09 Taiyo Yuden Co Ltd Piezoelectric ceramic composition, method for producing piezoelectric ceramic composition and piezoelectric ceramic component
WO2012044313A1 (en) * 2010-09-30 2012-04-05 Hewlett-Packard Development Company, L.P. Lead-free piezoelectric materials with enhanced fatigue resistance
US8734670B2 (en) 2010-09-30 2014-05-27 Hewlett-Packard Development Company, L.P. Lead-free piezoelectric materials with enhanced fatigue resistance
JP2016115752A (en) * 2014-12-12 2016-06-23 Tdk株式会社 Piezoelectric composition and piezoelectric element

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