JPH0269352A - Piezoelectric ceramics - Google Patents

Piezoelectric ceramics

Info

Publication number
JPH0269352A
JPH0269352A JP63222022A JP22202288A JPH0269352A JP H0269352 A JPH0269352 A JP H0269352A JP 63222022 A JP63222022 A JP 63222022A JP 22202288 A JP22202288 A JP 22202288A JP H0269352 A JPH0269352 A JP H0269352A
Authority
JP
Japan
Prior art keywords
tio2
crystal structure
piezoelectric ceramics
dried
rutile type
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.)
Pending
Application number
JP63222022A
Other languages
Japanese (ja)
Inventor
Masakatsu Kiyohara
正勝 清原
Mitsuhide Shimobukikoshi
光秀 下吹越
Akira Shimomura
下村 彰
Shigeru Kojima
茂 小島
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.)
Toto Ltd
Original Assignee
Toto 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 Toto Ltd filed Critical Toto Ltd
Priority to JP63222022A priority Critical patent/JPH0269352A/en
Publication of JPH0269352A publication Critical patent/JPH0269352A/en
Pending legal-status Critical Current

Links

Landscapes

  • Compositions Of Oxide Ceramics (AREA)

Abstract

PURPOSE:To improve piezoelectric characteristics by using TiO2 the main crystal structure of which is rutile type as the essential raw material. CONSTITUTION:The TiO2 is heated to change the crystal structure thereof from anatase type to rutile type and to obtain the TiO2 which is the rutile type in >=97% of the crystal structure. This TiO2 and respective carbonates or oxides of Pb, Mg, Nd, and Zr are wet mixed in a ball mill and are dried, then the dried mixture is subjected to preliminary calcination and pulverizing to obtain the pulverized matter. This pulverized matter is dried and a binder is added thereto. The pulverized matter is then molded and calcined by which the piezoelectric ceramics of the formula Pb(Mg1/3Nb2/3)O3-PbTiO2-PbZrO3 system is obtd.

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は電気的エネルギーと機械的エネルギーとの変換
を行う素子として用いる圧電セラミックスに関する。
DETAILED DESCRIPTION OF THE INVENTION (Field of Industrial Application) The present invention relates to piezoelectric ceramics used as elements that convert electrical energy to mechanical energy.

(従来の技術) アクチュエータ、ライターの着火素子或いはセンサー等
として用いる圧電セラミックスとして、2成分系のPb
ZrO3−PbT103に代わる3成分系のPb(Mg
%Nb%) 03−PbT103−PbZyOiが特公
昭42−9716号として知られ、更に上記組成中のp
b原子の一部をSrで置換したものが特公昭44−17
103号として提案され、各種特性に優れた圧電セラミ
ックスとして知られている。
(Prior art) Two-component Pb is used as piezoelectric ceramics used as actuators, lighter ignition elements, sensors, etc.
Three-component system Pb(Mg
%Nb%) 03-PbT103-PbZyOi is known as Japanese Patent Publication No. 42-9716, and further p in the above composition.
The one in which a part of the b atoms were replaced with Sr was published in 1977.
It was proposed as No. 103 and is known as a piezoelectric ceramic with excellent various properties.

(発明が解決しようとする課題) 上述したように最近では各種特性に優れた圧電セラミッ
クスが提案されているが、更なる特性の向上が望まれる
。例えばアクチュエータ等として用いる圧電セラミック
スにあっては、比誘電率(ε3./ε。)が小さく、圧
電歪定数(d3h)及び電気機械結合係数(KP)が゛
大きいことが好ましく、現在のものよりも更なる改良が
望まれる。
(Problems to be Solved by the Invention) As described above, piezoelectric ceramics with excellent various properties have recently been proposed, but further improvements in properties are desired. For example, for piezoelectric ceramics used as actuators, etc., it is preferable that the dielectric constant (ε3./ε.) is small and the piezoelectric strain constant (d3h) and electromechanical coupling coefficient (KP) are large. Further improvements are desired.

(課題を解決するための手段) 上記課題を解決すべく本発明は、圧電セラミックスの出
発原料として用いるTiO2として、その結晶構造の9
7%以上がルチル(高温型)で残りがアナターゼ(低温
型)となっているものとした。
(Means for Solving the Problems) In order to solve the above problems, the present invention provides that TiO2 used as a starting material for piezoelectric ceramics has a crystal structure of
It was assumed that 7% or more was rutile (high temperature type) and the rest was anatase (low temperature type).

(作用) TIO□を加熱することでその結晶構造をアナタ−セか
らルチルに変化せしめ、結晶構造がルチルとなっている
Tムロ2を用いることで焼成された圧電セラミックスの
特性が向上する。
(Function) By heating TIO□, its crystal structure changes from anatase to rutile, and by using TMURO 2 whose crystal structure is rutile, the characteristics of the fired piezoelectric ceramics are improved.

(実施例) 以下に具体的数値等を挙げて本発明の詳細な説明する。(Example) The present invention will be described in detail below with reference to specific numerical values.

先ず本発明にあっては人手したTiO2(rJ!L化チ
タフチタンアナターゼ熱して、その結晶構造のうち97
%以上を第1図に示すようなルチル(高温型)とし、残
りをアナターゼ(低温型)とする。実験では、加熱条件
を1000〜1200℃の温度で変化させ、アナターゼ
をルチル化し各種ルチル化率の異なったT、O,原料を
作成した。又、ルチル化率はX線回折法により求めた。
First, in the present invention, 97% of the crystal structure of TiO2 (rJ!L titanium anatase) is heated.
% or more is rutile (high temperature type) as shown in Figure 1, and the rest is anatase (low temperature type). In the experiment, anatase was rutiled by changing the heating conditions at a temperature of 1000 to 1200°C to create T, O, and raw materials with different rutile rates. Moreover, the rutilation rate was determined by X-ray diffraction method.

次いで加熱処理したTr02を用いて以下の組成物を得
る。
Next, the following composition is obtained using the heat-treated Tr02.

37 、5Pb (Mg% Nb% ) 03”37P
 bT 103”25 、5PbZr03以上の組成か
らなる組成物から圧電セラミックス(素子)を作成する
には以下の手順で行う。
37, 5Pb (Mg% Nb%) 03”37P
A piezoelectric ceramic (element) is produced from a composition having a composition of bT 103''25 , 5PbZr03 or more using the following procedure.

先ず予じめルチル化させたTIO□の他に化学的純度9
8%以上の酸化物又は炭酸塩を用意し、これらを原料と
して上記各式の配合組成となるように秤量し、ゴム内張
りをしたボールミルにて12時時間式混合を行って均一
な混合物とする。そしてこの混合物を乾燥せしめた後8
50℃で2時間予備焼成を行い、次いでボールミルにて
12時時間式粉砕する。この後粉砕物を乾燥せしめ、少
量の有機バインダーを加えて整粒したものを圧力100
0Kg/cm2で直径22mm厚さ2mmの円板に成形
し、この円板をルツボの密閉容器内で所定の温度で2時
間保持し焼成する。ここで所定の温度とは、1260℃
、 1270℃、1280℃及び1290℃の4水準と
した。
First, in addition to pre-rutilized TIO□, chemical purity 9
Prepare 8% or more oxides or carbonates, weigh them as raw materials so that they have the compounding composition of each formula above, and perform 12-hour mixing in a rubber-lined ball mill to make a homogeneous mixture. . After drying this mixture,
Preliminary firing was carried out at 50° C. for 2 hours, followed by pulverization for 12 hours in a ball mill. After that, the pulverized material was dried, a small amount of organic binder was added, and the granules were sized at a pressure of 100.
It is molded into a disk with a diameter of 22 mm and a thickness of 2 mm at 0 kg/cm2, and this disk is held and fired at a predetermined temperature for 2 hours in a closed container of a crucible. Here, the predetermined temperature is 1260℃
, 1270°C, 1280°C, and 1290°C.

次いで焼成した円板を研磨した後、円板の両面にg!電
極を塗布して焼付け、更にシリコンオイル中に侵潰し常
温で2.5kv/+mの直流電界を20分間印加し分極
を行うことで目的とする圧電セラミックスを得る。
Next, after polishing the fired disc, g! is applied to both sides of the disc. The desired piezoelectric ceramics are obtained by applying an electrode, baking it, immersing it in silicone oil, and applying a DC electric field of 2.5 kv/+m for 20 minutes at room temperature to perform polarization.

以上によって得られた圧電セラミックス(ルチル化率9
7%及び100%)と、従来の圧電セラミックス即ち結
晶構造がアナターゼ100%及びルチル93%ものとの
特性を比較した結果を第2図乃至第5図に示す。ここで
図中の記号の意味は以下の通りである。
The piezoelectric ceramics obtained as above (rutilation rate 9
7% and 100%) and conventional piezoelectric ceramics, that is, those whose crystal structures are 100% anatase and 93% rutile, are shown in FIGS. 2 to 5. Here, the meanings of the symbols in the figure are as follows.

ε33/ε。:比誘電率。ε33/ε. : Specific dielectric constant.

Kp(%F)  :電気機械結合係数。この値は大きい
方が圧電セラミックスとしての特性に優れる。
Kp (%F): Electromechanical coupling coefficient. The larger this value is, the better the properties of piezoelectric ceramics will be.

d3□ :圧電歪定数。電圧を印加した場合に印加方向
に対して直交する方向のひずみ。この値が大きければア
クチュエータ等として用いる場合の特性が優れる。
d3□: Piezoelectric strain constant. Strain in the direction perpendicular to the direction of application when voltage is applied. The larger this value, the better the characteristics when used as an actuator or the like.

(発明の効果) 以上の説明及び第2図乃至第4図に示した結果から明ら
かなように本発明によれば、T、02を出発原料として
用いる場合に、当該TiO2の結晶構造が97%以上が
ルチルとなるようにしたことで、従来よりも優れた圧電
特性を発揮する圧電セラミックスが得られる。
(Effects of the Invention) As is clear from the above explanation and the results shown in FIGS. 2 to 4, according to the present invention, when T,02 is used as a starting material, the crystal structure of TiO2 is 97% By making the above material rutile, it is possible to obtain piezoelectric ceramics that exhibit piezoelectric properties superior to those of conventional ceramics.

【図面の簡単な説明】[Brief explanation of the drawing]

第1図はTiO7の結晶構造を示す図、第2図乃至第4
図は本発明に係る圧電セラミックスと従来の圧電セラミ
ックスとの特性を比較したグラフである。
Figure 1 shows the crystal structure of TiO7, Figures 2 to 4
The figure is a graph comparing the characteristics of the piezoelectric ceramic according to the present invention and the conventional piezoelectric ceramic.

Claims (2)

【特許請求の範囲】[Claims] (1)TiO_2(酸化チタン)を出発原料の一部とし
て用いた圧電セラミックスにおいて、前記TiO_2の
結晶構造は97%以上がルチルであることを特徴とする
圧電セラミックス。
(1) A piezoelectric ceramic using TiO_2 (titanium oxide) as a part of the starting material, wherein the crystal structure of the TiO_2 is 97% or more of rutile.
(2)前記圧電セラミックスはPb(Mg_1_/_3
Nb_2_/_3)O_3−PbTiO_3−PbZr
O_3系のものであることを特徴とする請求項1に記載
の圧電セラミックス。
(2) The piezoelectric ceramic is Pb(Mg_1_/_3
Nb_2_/_3)O_3-PbTiO_3-PbZr
The piezoelectric ceramic according to claim 1, wherein the piezoelectric ceramic is O_3-based.
JP63222022A 1988-09-05 1988-09-05 Piezoelectric ceramics Pending JPH0269352A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP63222022A JPH0269352A (en) 1988-09-05 1988-09-05 Piezoelectric ceramics

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP63222022A JPH0269352A (en) 1988-09-05 1988-09-05 Piezoelectric ceramics

Publications (1)

Publication Number Publication Date
JPH0269352A true JPH0269352A (en) 1990-03-08

Family

ID=16775874

Family Applications (1)

Application Number Title Priority Date Filing Date
JP63222022A Pending JPH0269352A (en) 1988-09-05 1988-09-05 Piezoelectric ceramics

Country Status (1)

Country Link
JP (1) JPH0269352A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100403302B1 (en) * 2000-12-16 2003-10-30 주식회사 에스세라 A method for preparing Pb-based peizoelectric ceramic powder containing the carbonate
US7056443B2 (en) * 2002-05-30 2006-06-06 Tdk Corporation Piezoelectric ceramic production method and piezoelectric element production method

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5590465A (en) * 1978-12-29 1980-07-09 Matsushita Electric Industrial Co Ltd Manufacture of piezoelectric ceramic
JPS5678424A (en) * 1979-11-26 1981-06-27 Matsushita Electric Ind Co Ltd Preparation of compound titanium oxide
JPS56149710A (en) * 1980-04-23 1981-11-19 Matsushita Electric Industrial Co Ltd Method of manufacturing lead titanate

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5590465A (en) * 1978-12-29 1980-07-09 Matsushita Electric Industrial Co Ltd Manufacture of piezoelectric ceramic
JPS5678424A (en) * 1979-11-26 1981-06-27 Matsushita Electric Ind Co Ltd Preparation of compound titanium oxide
JPS56149710A (en) * 1980-04-23 1981-11-19 Matsushita Electric Industrial Co Ltd Method of manufacturing lead titanate

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100403302B1 (en) * 2000-12-16 2003-10-30 주식회사 에스세라 A method for preparing Pb-based peizoelectric ceramic powder containing the carbonate
US7056443B2 (en) * 2002-05-30 2006-06-06 Tdk Corporation Piezoelectric ceramic production method and piezoelectric element production method

Similar Documents

Publication Publication Date Title
JP2002068835A (en) Piezoelectric ceramic composition
KR20130128378A (en) Lead-free piezoelectric materials with enhanced fatigue resistance
KR101635939B1 (en) Bismuth-based lead-free piezoelectric ceramics and Actuator using the same
US2729757A (en) Ferroelectric ceramic composition and method of making same
JPH04130682A (en) Piezoelectric ceramic composition for actuator
KR930002641B1 (en) Ferroelectric ceramics
JPH0269352A (en) Piezoelectric ceramics
US3021441A (en) Piezoelectric transducer
JPH0339028B2 (en)
US3994823A (en) Ceramic material and method of making
KR100875479B1 (en) Lead-free piezoelectric ceramic composition and its manufacturing method
Promjun et al. Effect of Nb, Ta and Sb addition on structure and electrical properties of PZT ceramics
JP3781317B2 (en) Piezoelectric ceramic material
US3400076A (en) Piezoelectric ceramic compositions
JP3629933B2 (en) Method for producing crystal-oriented ceramics
JP2660301B2 (en) Manufacturing method of sintered body
JP3802611B2 (en) Piezoelectric material
JP2570662B2 (en) Ferroelectric porcelain
KR101635993B1 (en) Lead-free piezoelectric ceramics and Actuator using the same
JPS6358777B2 (en)
JPH0196973A (en) Manufacture of piezoelectric porcelain
JP2841344B2 (en) Piezoelectric ceramic composition
CN118145997A (en) Sodium niobate-based ferroelectric ceramics prepared using calcium carbonate powder and preparation method thereof
RU2130000C1 (en) Electrostrictive material
JPH04260662A (en) Piezoelectric ceramic composition