Piezoelectric composite material

• US 4,675,123 A
• Filed: 04/11/1985
• Issued: 06/23/1987
• Est. Priority Date: 01/17/1979
• Status: Expired due to Term

• Current Assignee: NGK Spark PLUG Company Limited
• Original Assignee: NGK Spark PLUG Company Limited
• Inventors: Ito, Hiroshi, Yamamoto, Takashi, Tsunooka, Tsutomu, Saito, Shigeo
• Primary Examiner(s): Cooper, Jack
• Application Number:
  US06/722,199
• Time in Patent Office: 803 Days
• Field of Search: 252/62.9
• US Class Current: 252/62.90R
• CPC Class Codes: H10N 30/092 Forming composite materials
• CPC Class Codes: H10N 30/852 Composite materials, e.g. having 1-3 or 2-2 type connectivity

Abstract

A piezoelectric composite material having excellent piezoelectric property and workability, which is prepared by compounding in a specific mixing ratio a ferroelectric ceramic powder comprising microcrystals having uniform size and virtually a single domain and a polymer. The ceramic powder is obtained by preparing a ceramic having a desired composition by causing the appropriate mixture of starting powders to undergo a solid phase reaction, grinding the reaction product, annealing the resulting powder under heat and optionally chemically etching it.

Claims

1. A ferroelectric, pyroelectric or piezoelectric composite material comprising a mixture of one or more polymers and a ferroelectric ceramic powder which contains 90% or more grains in a particle size range of about 1 μ

m to about 3 mm at a ceramic powder;

polymer(s) mixing ratio of about 1;

9 to 9;

1 by volume, said ferroelectric ceramic powder comprising microcrystals having virtually single domains and being prepared by mixing starting powders in amounts corresponding to the desired chemical composition of the ferroelectric ceramic powder, subjecting the mixed powders to a solid phase reaction, mechanically grinding the reaction product into powder, whereby multiple domains or distorted phases are formed, and then heat annealing the ground powder at a temperature sufficient to reform the multiple domains or distorted phases to virtually single domains.

2. The composite material of claim 1, wherein said heat annealing is carried out at about 600°

to 1200°

C. in air or in an atmosphere having an O₂ concentration of about 21% to 100% for about 1 to 30 hours.

3. The composite material of claim 1, wherein said polymer is a natural rubber or a synthetic rubber or a thermoplastic resin.

4. The composite material of claim 1, wherein said heat-annealing treatment is carried out 2 to 4 times.

5. The composite material of claim 1, wherein said ferroelectric ceramic powder contains as a basic composition the following one-, two or three-component systems:

I. Perovskite structures selected from (1) to (5);

(1) barium titanate and solid solutions containing as the main component barium titanate;

(2) lead titanate and solid solutions containing as the main component lead titanate;

(3) lead titanate zirconate and solid solutions containing this salt as the main component;

(4) three-component ceramics consisting of solid solutions containing lead titanate zirconate and as a third component a salt of lead oxide and other metal oxides belonging to one of the following groups (a) to (f);

(a) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.2+ (B.sub.1/3.sup.2+.B.sub.2/3.sup.5+)O.sub.3

where A²⁺ is Pb, Sr or Ba;

B²⁺ is Zn, Cd, Mg, Ni or Co and B⁵⁺ is Nb or Ta;

(b) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.2+ (B.sub.1/2.sup.2+.B.sub.1/2.sup.6+)O.sub.3

where A²⁺ is Pb;

B²⁺ is Cd, Mn, Zn, Mg, Co or Ni and B⁶⁺ is W or Te;

(c) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.2+ (B.sub.1/2.sup.3+.B.sub.1/2.sup.5+)O.sub.3

where A²⁺ is Pb, Ba or Ca;

B³⁺ is Fe, Sc, Cr, Yb, Lu or In and B⁵⁺ is Nb or Ta;

(d) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.2+ (B.sub.2/3.sup.3+.B.sub.1/3.sup.6+)O.sub.3

wherein A²⁺ is Pb;

B³⁺ is Fe and B⁶⁺ is W;

(e) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.3+ (B.sub.1/2.sup.2+.B.sub.1/2.sup.4+)O.sub.3

wherein A³⁺ is La or Nd;

B²⁺ is Mg and B⁴⁺ is Ti;

(f) oxides represented by the formula;

space="preserve" listing-type="equation">(A.sub.1/2.sup.1+.A.sub.1/2.sup.3+)BO.sub.3

wherein A¹⁺ is Na or K;

A³⁺ is La, Ce, Nd or Bi and B is Ti; and

(5) solid solutions containing NaNbO₃ ;

II. tungsten bronze structures;

III. bismuth layer structures;

IV. LiNbO₃ or LiTaO₃ ;

ceramics which containing as a basic composition the above one-, two- or three-component systems, wherein a part of the Pb is replaced by an alkaline earth metal(s);

ceramics which contain as a basic composition the above one-, two- or three-component systems and further contain, as a supplemental component, one or more oxides selected from the following groups I, II or III for the purpose of modification;

I. Nb₂ O₅, Ta₂ O₅, La₂ O₃, Sb₂ O₅, Sb₂ O₃, Bi₂ O₃ and WO₃ ;

II. MgO, Fe₂ O₃, Sc₂ O₃ and K₂ O; and

III. Cr₂ O₃, U₂ O₃ and MnO₂ ; and

ceramics which contain as a basic composition the above-described one-, two- or three-component systems, wherein the Pb component is present in excess of the stoichiometric amount.

6. A ferroelectric, pyroelectric or piezoelectric composite material comprising a mixture of one or more polymers and a ferroelectric ceramic powder which contains 90% or more grains in a particle size range of about 1 μ

m to about 3 mm at a ceramic powder;

polymer(s) mixing ratio of about 1;

9 to 9;

1 by volume, said ferroelectric ceramic powder comprising microcrystals having virtually single domains and being prepared by mixing starting powders in amounts corresponding to the desired chemical composition of the ferroelectric ceramic powder, subjecting the mixed starting powders to a solid phase reaction, mechanically grinding the reaction product into powder, whereby multiple domains or distorted phases are formed, then heat annealing the ground powder at a temperature sufficient to reform the multiple domains or distorted phases to virtually single domains, and further subjecting the annealed powder to chemical etching in an etching solution under mild conditions such that the distorted phases and amorphous phases present are removed.

7. The composite material of claim 6, wherein said chemical etching treatment is accompanied by stirring or light grinding.

8. The composite material of claim 6, wherein said heat annealing is carried out at about 600°

to 1200°

C. in air or in an atmosphere having an O₂ concentration of about 21% to 100% for about 1 to 30 hours.

9. The composite material of claim 6, wherein said polymer is a natural rubber or a synthetic rubber or a thermoplastic resin.

10. The composite material of claim 6, wherein said heat-annealing treatment is carried out 2 to 4 times.

11. The composite material of claim 6, wherein etching is carried out using an acid or alkali solution having a pH of about 3 or less or about 13 or more, respectively, or using hydrogen peroxide.

12. The composite material of claim 6, wherein said ferroelectric ceramic powder contains as a basic composition the following one-, two or three-component systems:

I. Perovskite structures selected from (1) to (5);

(1) barium titanate and solid solutions containing as the main component barium titanate;

(2) lead titanate and solid solutions containing as the main component lead titanate;

(3) lead titanate zirconate and solid solutions containing this salt as the main component;

(4) three-component ceramics consisting of solid solutions containing lead titanate zirconate and as a third component a salt of lead oxide and other metal oxides belonging to one of the following groups (a) to (f);

(a) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.2+ (B.sub.1/3.sup.2+.B.sub.2/3.sup.5+)O.sub.3

where A²⁺ is Pb, Sr or Ba;

B²⁺ is Zn, Cd, Mg, Ni or Co and B⁵⁺ is Nb or Ta;

(b) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.2+ (B.sub.1/2.sup.2+.B.sub.1/2.sup.6+)O.sub.3

where A²⁺ is Pb;

B²⁺ is Cd, Mn, Zn, Mg, Co or Ni and B⁶⁺ is W or Te;

(c) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.2+ (B.sub.1/2.sup.3+.B.sub.1/2.sup.5+)O.sub.3

where A²⁺ is Pb, Ba or Ca;

B³⁺ is Fe, Sc, Cr, Yb, Lu or In and B⁵⁺ is Nb or Ta;

(d) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.2+ (B.sub.2/3.sup.3+.B.sub.1/3.sup.6+)O.sub.3

wherein A²⁺ is Pb;

B³⁺ is Fe and B⁶⁺ is W;

(e) oxides represented by the formula;

space="preserve" listing-type="equation">A.sup.3+ (B.sub.1/2.sup.2+.B.sub.1/2.sup.4+)O.sub.3

wherein A³⁺ is La or Nd;

B²⁺ is Mg and B⁴⁺ is Ti;

(f) oxides represented by the formula;

space="preserve" listing-type="equation">(A.sub.1/2.sup.1+.A.sub.1/2.sup.3+)BO.sub.3

wherein A¹⁺ is Na or K;

A³⁺ is La, Ce, Nd or Bi and B is Ti; and

(5) solid solutions containing NaNbO₃ ;

II. tungsten bronze structures;

III. bismuth layer structures;

IV. LiNbO₃ or LiTaO₃ ;

cermaics which containing as a basic composition the above one-, two- or three-component systems, wherein a part of the Pb is replaced by an alkaline earth metal(s);

ceramics which contain as a basic composition the above one-, two- or three-component systems and further contain, as a supplemental component, one or more oxides selected from the following groups I, II or III for the purpose of modification;

I. Nb₂ O₅, Ta₂ O₅, La₂ O₃, Sb₂ O₅, Sb₂ O₃, Bi₂ O₃ and WO₃ ;

II. MgO, Fe₂ O₃, Sc₂ O₃ and K₂ O; and

III. Cr₂ O₃, U₂ O₃ and MnO₂ ; and

ceramics which contain as a basic composition the above-described one-, two- or three-component systems, wherein the Pb component is present in excess of the stoichiometric amount.

13. A ferroelectric, pyroelectric or piezoelectric composite material comprising a mixture of one or more polymers and ferroelectric single crystal powder which contains 90% or more grains in a particle size range of about 1 μ

m to about 3 mm at a single crystal powder;

polymer(s) mixing ratio of about 1;

9 to 9;

1 by volume, said ferroelectric single crystal powder comprising microcrystals having virtually single domains and being prepared by grinding a single crystal until the resulting powder has the desired particle size, whereby multiple domains or distorted phases are formed, and heat annealing the thus ground powder at a temperature sufficient to reform the multiple doamins or distorted phases to virtually single domains.

14. The composite material of claim 13, wherein said heat annealing is carried out at about 600°

to 1200°

C. in air or in an atmosphere having an O₂ concentration of about 21% to 100% for about 1 to 30 hours.

15. The composite material of claim 13, wherein said polymer is a natural rubber or a synthetic rubber or a thermoplastic resin.

16. The composite material of claim 13, wherein said heat-annealing treatment is carried out 2 to 4 times.

17. A ferroelectric, pyroelectric or piezoelectric composite material comprising a mixture of one or more polymers and a ferroelectric single crystal powder which contains 90% or more grains in a particle size range of about 1 μ

m to about 3 mm at a single crystal powder;

polymer(s) mixing ratio of about 1;

9 to 9;

1 by volume, said ferroelectric single crystal powder comprising microcrystals having virtually single domains and being prepared by grinding a single crystal until the resulting powder has the desired particle size, whereby multiple domains or distorted phases are formed, heat annealing the thus ground powder at a temperature sufficient to reform the multiple domains or distorted phases to virtually single domains and further subjecting the annealed powder to chemical etching in an etching solution under mild conditions such that the distorted phases and amorphous phases present are removed.

18. The composite material of claim 17, wherein said chemical etching treatment is accompanied by stirring or light grinding.

19. The composite material of claim 17, wherein said heat annealing is carried out at about 600°

to 1200°

C. in air or in an atmosphere having an O₂ concentration of about 21% to 100% for about 1 to 30 hours.

20. The composite material of claim 17, wherein said polymer is a natural rubber or a synthetic rubber or a thermoplastic resin.

21. The composite material of claim 17, wherein said heat-annealing treatment is carried out 2 to 4 times.

22. The composite material of claim 17, wherein etching is carried out using an acid or alkali solution having a pH of about 3 or less or about 13 or more, respectively, or using hydrogen peroxide.