JP3163664B2 - Piezoelectric material - Google Patents

Piezoelectric material

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Publication number
JP3163664B2
JP3163664B2 JP20127591A JP20127591A JP3163664B2 JP 3163664 B2 JP3163664 B2 JP 3163664B2 JP 20127591 A JP20127591 A JP 20127591A JP 20127591 A JP20127591 A JP 20127591A JP 3163664 B2 JP3163664 B2 JP 3163664B2
Authority
JP
Japan
Prior art keywords
firing
amount
lead
lead oxide
sio
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 - Lifetime
Application number
JP20127591A
Other languages
Japanese (ja)
Other versions
JPH0524916A (en
Inventor
部 正 嘉 勝
里 修 西
村 明 修 高
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.)
Murata Manufacturing Co Ltd
Original Assignee
Murata Manufacturing Co Ltd
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 Murata Manufacturing Co Ltd filed Critical Murata Manufacturing Co Ltd
Priority to JP20127591A priority Critical patent/JP3163664B2/en
Publication of JPH0524916A publication Critical patent/JPH0524916A/en
Application granted granted Critical
Publication of JP3163664B2 publication Critical patent/JP3163664B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

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Description

【発明の詳細な説明】DETAILED DESCRIPTION OF THE INVENTION

【0001】[0001]

【産業上の利用分野】この発明は圧電磁器材料に関し、
特にたとえば通信機用圧電フィルタなどに用いられる、
圧電磁器材料に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a piezoelectric ceramic material,
In particular, for example, used for piezoelectric filters for communication equipment,
Related to piezoelectric ceramic materials.

【0002】[0002]

【従来の技術】従来、通信機用圧電フィルタなどに、
{PbSr}{(TiZr)(MnNb)}O3 系の圧
電磁器材料が用いられている。
2. Description of the Related Art Conventionally, piezoelectric filters for communication devices have been used.
A {PbSr} (TiZr) (MnNb)} O 3 -based piezoelectric ceramic material is used.

【0003】[0003]

【発明が解決しようとする課題】しかしながら、このよ
うな従来の圧電磁器材料では、焼成時に酸化鉛の蒸発が
約0.8重量%も発生し、焼成炉中に高濃度の鉛雰囲気
を形成していた。これによって、鉛雰囲気の濃度勾配な
どの焼結性を阻害する要因が生じ、焼結体の変形不良な
どを発生させていた。この酸化鉛の蒸発量を抑制するに
は、適当な手段がなく、焼成温度,焼成排風量,匣密度
などの外的手段で行っており、コスト面などでリスクが
大きい。また、従来の材料では、焼成温度が1250℃
以上と高く、また、得られた焼結体の電気的特性にばら
つきが生じる。
However, in such a conventional piezoelectric ceramic material, about 0.8% by weight of lead oxide evaporates during firing, and a high-concentration lead atmosphere is formed in the firing furnace. I was As a result, factors that hinder sinterability, such as a concentration gradient in a lead atmosphere, are generated, and defective deformation of the sintered body is caused. In order to suppress the amount of lead oxide evaporated, there is no suitable means, but external means such as firing temperature, firing exhaust air volume, box density and the like are used. In the case of a conventional material, the firing temperature is 1250 ° C.
The above is high, and the electrical characteristics of the obtained sintered body vary.

【0004】それゆえに、この発明の主たる目的は、焼
成する際の酸化鉛蒸発量を抑制し、焼成時の鉛雰囲気状
態をコントロールし、低温で焼結でき、焼結体の電気的
特性のばらつきを改善することができる、圧電磁器材料
を提供することである。
[0004] Therefore, a main object of the present invention is to suppress the amount of lead oxide evaporated during firing, control the lead atmosphere during firing, sinter at a low temperature, and vary the electrical characteristics of the sintered body. It is an object of the present invention to provide a piezoelectric ceramic material capable of improving

【0005】[0005]

【課題を解決するための手段】この発明は、{PbS
r}{(TiZr)(MnNb)}O3 系の圧電磁器材
料において、SiO2 を0.005〜0.040重量%
およびAl2 3 を0.005〜0.040重量%含
することを特徴とする、圧電磁器材料である。
Means for Solving the Problems The present invention provides a {PbS
r} {(TiZr) (MnNb)} O 3 -based piezoelectric ceramic material containing 0.005 to 0.040% by weight of SiO 2
And Al 2 O 3 and having containing 0.005 to 0.040% by weight, a piezoelectric ceramic material.

【0006】[0006]

【作用】SiO2 およびAl2 3 を添加することによ
って、焼成時に、これらの添加物と鉛との化合物が形成
される。それによって、焼成時における酸化鉛の蒸発量
が抑制される。また、これらの添加物の添加量によっ
て、焼成時における焼成炉中の鉛雰囲気の状態がコント
ロールされる。
By adding SiO 2 and Al 2 O 3 , a compound of these additives and lead is formed during firing. Thereby, the amount of evaporation of the lead oxide during firing is suppressed. The amount of these additives controls the state of the lead atmosphere in the firing furnace during firing.

【0007】さらに、形成されたSi化合物やAl化合
物は低融点物質であるため、焼成時における材料の拡散
性が向上する。
Further, since the formed Si compound or Al compound is a low melting point substance, the diffusivity of the material during firing is improved.

【0008】[0008]

【発明の効果】この発明によれば、酸化鉛の蒸発量が抑
制されるため、焼成時の鉛雰囲気の濃度勾配などの焼結
性を阻害する要因が軽減され、変形不良の改善などに効
果的である。さらに、SiO2 およびAl2 3 の添加
量によって、焼成時の鉛雰囲気状態がコントロールされ
るため、従来のような焼成温度,焼成排風量,匣密度な
どの外的手段が軽減できる。
According to the present invention, since the evaporation amount of lead oxide is suppressed, factors that hinder sintering, such as the concentration gradient of the lead atmosphere during firing, are reduced, which is effective in improving deformation defects. It is a target. Furthermore, since the lead atmosphere during firing is controlled by the addition amounts of SiO 2 and Al 2 O 3 , external means such as the conventional firing temperature, firing air volume, and box density can be reduced.

【0009】また、Si化合物,Al化合物の形成によ
って、材料の拡散力が向上するため、低温焼成化や焼結
安定温度域の拡張が図れ、焼結体のばらつき、すなわち
電気特性としての電気機械結合係数の分散を縮小するこ
とができる。
Further, since the diffusing power of the material is improved by the formation of the Si compound and the Al compound, low-temperature sintering and expansion of the sintering stable temperature range can be achieved, and the variation of the sintered body, that is, the electric mechanical property The variance of the coupling coefficient can be reduced.

【0010】この発明の上述の目的,その他の目的,特
徴および利点は、図面を参照して行う以下の実施例の詳
細な説明から一層明らかとなろう。
The above objects, other objects, features and advantages of the present invention will become more apparent from the following detailed description of embodiments with reference to the drawings.

【0011】[0011]

【実施例】{PbSr}{(TiZr)(MnNb)}
3 系の圧電磁器材料の製造工程において、PbO,T
iO2 ,ZrO2 などの素原料を調合する工程、あるい
はこれらの仮焼物にバインダなどを添加する工程でS
2 とAl2 3 との両方を一定量添加する。
[Example] {PbSr} (TiZr) (MnNb)}
In the manufacturing process of O 3 -based piezoelectric ceramic materials, PbO, T
In the step of preparing raw materials such as iO 2 and ZrO 2 , or in the step of adding a binder or the like to these calcined materials, Si
A fixed amount of both O 2 and Al 2 O 3 is added.

【0012】これを原料として、成形して焼成すると、
鉛とSiO2 およびAl2 3 との化合物が形成され
る。そして、未反応酸化鉛が減少し、焼成時の酸化鉛蒸
発量が抑制される。また、SiO2 およびAl2 3
添加量によって、酸化鉛蒸発量が変化する。そのため、
焼成時の酸化鉛蒸発量さらには焼成時の鉛雰囲気濃度
が、SiO2 およびAl2 3 の添加量で調整できる。
When this is used as a raw material and molded and fired,
A compound of lead and SiO 2 and Al 2 O 3 is formed. Then, unreacted lead oxide is reduced, and the amount of evaporated lead oxide during firing is suppressed. Further, the amount of lead oxide evaporated varies depending on the amount of SiO 2 and Al 2 O 3 added. for that reason,
The amount of lead oxide evaporated during firing and the concentration of lead atmosphere during firing can be adjusted by the addition amounts of SiO 2 and Al 2 O 3 .

【0013】さらに、Si化合物やAl化合物などの低
融点物質が形成されるため、焼結時の材料の拡散力が向
上し、低温で焼結でき、焼結体の電気的特性のばらつき
を改善することができる。
Further, since a low-melting substance such as a Si compound or an Al compound is formed, the diffusing power of the material at the time of sintering is improved, sintering can be performed at a low temperature, and variation in electrical characteristics of the sintered body is improved. can do.

【0014】(実施例1) まず、出発原料としてPbO,TiO2 ,ZrO2 ,S
rCO3 ,MnCO3およびNb2 5 を使用し、これ
らの粉末を{Pb1.00Sr0.01}{(Ti0.55
0.45)(Mn0.9 Nb0.1 0.01}O3 の化学式にな
るように秤量し、秤量物を得た。この秤量物にCr2
3 ,WO3 を一定量添加し、水を媒体に混合し粉砕し
て、スラリを得た。こうして得られたスラリを脱水し乾
燥した後、900℃で仮焼し、仮焼物を得た。さらに、
この仮焼物をハンマーミルで乾式粉砕し、再度水を媒体
としてポリビニルアルコール系バインダを1.5重量%
添加して、スラリを得た。このときに、SiO2 を0.
02〜0.04重量%およびAl23 を0.02〜
0.04重量%同時に添加し、十分な混合を行った。
(Example 1) First, PbO, TiO 2 , ZrO 2 , S
Using rCO 3 , MnCO 3 and Nb 2 O 5 , these powders were converted to {Pb 1.00 Sr 0.01 } (Ti 0.55 Z
r 0.45 ) (Mn 0.9 Nb 0.1 ) 0.01 } O 3 was weighed to obtain a chemical formula to obtain a weighed material. Cr 2 O
3 , a certain amount of WO 3 was added, water was mixed with the medium and pulverized to obtain a slurry. The slurry thus obtained was dehydrated and dried, and then calcined at 900 ° C. to obtain a calcined product. further,
The calcined product is dry-pulverized with a hammer mill, and a polyvinyl alcohol-based binder is again used as a medium in an amount of 1.5% by weight.
Upon addition, a slurry was obtained. At this time, SiO 2 was added to 0.1.
02-0.04% by weight and Al 2 O 3
0.04% by weight was added simultaneously, and sufficient mixing was performed.

【0015】このスラリをスプレドライヤによって造粒
し乾燥して、粉末を得た。この粉末をプレス機で、成形
圧1t/cm2 で25×35mmの角板状に成形して、
成形体を得た。こうして得られた成形体を一度脱バイン
ダを行う目的で700℃で仮焼成し、仮焼成体の重量を
測定後、再度1260℃で本焼成し、焼結体の重量を測
定した。
This slurry was granulated by a spray dryer and dried to obtain a powder. This powder by a press machine, and molded at a molding pressure of 1t / cm 2 to 25 × 35 mm of square plate-shaped,
A molded article was obtained. The molded body thus obtained was calcined at 700 ° C. for the purpose of once removing the binder, the weight of the calcined body was measured, and the calcined body was again calcined at 1260 ° C., and the weight of the sintered body was measured.

【0016】図1は一実施例および従来例の本焼成時の
重量減(%)を示すグラフである。。なお、本焼成時の
重量減(%)は、次式によって計算される。
FIG. 1 is a graph showing the weight loss (%) at the time of main firing of one embodiment and a conventional example. . The weight loss (%) at the time of the main firing is calculated by the following equation.

【0017】 [0017]

【0018】図1に示すように、本焼成時の重量減
(%)は、SiO2 およびAl2 3 を添加することに
よって減少する。すなわち、仮焼成(700℃)後の本
焼成時に蒸発する物質は、酸化鉛に限定されるため、S
iO2 およびAl2 3 と酸化鉛とが化合することによ
って、本焼成時の酸化鉛蒸発量が抑制できる。
As shown in FIG. 1, the weight loss (%) at the time of the main firing is reduced by adding SiO 2 and Al 2 O 3 . That is, the substance that evaporates during the main firing after the preliminary firing (700 ° C.) is limited to lead oxide.
By the combination of iO 2 and Al 2 O 3 with lead oxide, the amount of lead oxide evaporated during the main firing can be suppressed.

【0019】さらに、酸化鉛の蒸発量は、SiO2 およ
Al2 3 の添加量によって変化することから、本焼
成時の酸化鉛蒸発量さらには本焼成時の鉛雰囲気濃度
は、SiO2 およびAl2 3 の添加量によってコント
ロールできる。
Furthermore, the amount of lead oxide evaporated is SiO 2 and
And the amount of addition of Al 2 O 3, the amount of lead oxide evaporated during main firing and the concentration of lead atmosphere during main firing can be controlled by the amounts of SiO 2 and Al 2 O 3 added.

【0020】[0020]

【0021】[0021]

【0022】[0022]

【0023】[0023]

【0024】[0024]

【0025】[0025]

【0026】[0026]

【0027】[0027]

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

【図1】この発明の一実施例および従来例の本焼成時の
重量減(%)を示すグラフである。
FIG. 1 is a graph showing the weight loss (%) at the time of main firing of one embodiment of the present invention and a conventional example.

───────────────────────────────────────────────────── フロントページの続き (56)参考文献 特開 昭52−136399(JP,A) 特開 昭50−64799(JP,A) 特開 昭55−63890(JP,A) 特公 昭48−39640(JP,B1) (58)調査した分野(Int.Cl.7,DB名) C04B 35/42 - 35/49 CA(STN) REGISTRY(STN)──────────────────────────────────────────────────続 き Continuation of the front page (56) References JP-A-52-136399 (JP, A) JP-A-50-64799 (JP, A) JP-A-55-63890 (JP, A) 39640 (JP, B1) (58) Field surveyed (Int. Cl. 7 , DB name) C04B 35/42-35/49 CA (STN) REGISTRY (STN)

Claims (1)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】 {PbSr}{(TiZr)(MnN
b)}O3 系の圧電磁器材料において、 SiO2 を0.005〜0.040重量%およびAl2
3 を0.005〜0.040重量%含有することを特
徴とする、圧電磁器材料。
1. {PbSr} (TiZr) (MnN
b) In an O 3 -based piezoelectric ceramic material, 0.005 to 0.040% by weight of SiO 2 and Al 2
O 3, and having containing 0.005 to 0.040 wt%, the piezoelectric ceramic material.
JP20127591A 1991-07-15 1991-07-15 Piezoelectric material Expired - Lifetime JP3163664B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP20127591A JP3163664B2 (en) 1991-07-15 1991-07-15 Piezoelectric material

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP20127591A JP3163664B2 (en) 1991-07-15 1991-07-15 Piezoelectric material

Publications (2)

Publication Number Publication Date
JPH0524916A JPH0524916A (en) 1993-02-02
JP3163664B2 true JP3163664B2 (en) 2001-05-08

Family

ID=16438266

Family Applications (1)

Application Number Title Priority Date Filing Date
JP20127591A Expired - Lifetime JP3163664B2 (en) 1991-07-15 1991-07-15 Piezoelectric material

Country Status (1)

Country Link
JP (1) JP3163664B2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3570294B2 (en) * 1999-05-20 2004-09-29 株式会社村田製作所 Piezoelectric ceramic material and piezoelectric ceramic sintered body obtained using the same
JP3562402B2 (en) * 1999-09-29 2004-09-08 株式会社村田製作所 Piezoelectric ceramic material and surface wave device using the same
JP3783534B2 (en) * 2000-08-18 2006-06-07 株式会社村田製作所 Piezoelectric ceramic sintered body and piezoelectric ceramic element
EP1728773A4 (en) * 2004-03-26 2009-08-19 Tdk Corp Piezoelectric ceramic composition

Also Published As

Publication number Publication date
JPH0524916A (en) 1993-02-02

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