WO2002079285A1 - Terpolymer systems for electromechanical and dielectric applications - Google Patents

Terpolymer systems for electromechanical and dielectric applications Download PDF

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Publication number
WO2002079285A1
WO2002079285A1 PCT/US2002/009181 US0209181W WO02079285A1 WO 2002079285 A1 WO2002079285 A1 WO 2002079285A1 US 0209181 W US0209181 W US 0209181W WO 02079285 A1 WO02079285 A1 WO 02079285A1
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Prior art keywords
polyvinylidene fluoride
trifluorethylene
tetrafluorethylene
fluoride
polymer
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PCT/US2002/009181
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French (fr)
Inventor
Qiming Zhang
Haisheng Xu
Zong Yang Cheng
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The Penn State Research Foundation
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Publication of WO2002079285A1 publication Critical patent/WO2002079285A1/en

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    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
    • C08F214/18—Monomers containing fluorine
    • C08F214/22—Vinylidene fluoride
    • C—CHEMISTRY; METALLURGY
    • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F214/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen
    • C08F214/18—Monomers containing fluorine
    • C08F214/26—Tetrafluoroethene

Definitions

  • the present invention relates to polymeric materials with elevated electric field induced strain levels, elevated elastic energy densities, and having elevated dielectric constants at room temperature.
  • the material can be used in electromechanical devices which convert electric energy into mechanical energy or convert mechanical energy into electric energy.
  • Material of the invention can also be used as a capacitor which stores electric energy and regulates electric voltage in a circuit.
  • strain level and elastic energy density both are quite low (strain ⁇ 0.1% and elastic density ⁇ 0.1 J/cm 3 ), which causes many problems for device performance.
  • an amplification scheme has to be used.
  • the low elastic energy density also reduces the force and power output of the electromechanical devices.
  • actuators and transducers there is a demand for improved materials for use in actuators and transducers due to the limitations of currently available materials.
  • current actuator materials such as electrostatic, electromagnetic and piezoelectric materials
  • piezoceramic and magnetostrictive materials while possessing low hysteresis and high response speeds, 5 suffer from low strain levels (-0.1 %).
  • Shape memory alloys generate high strain and high force but are often associated with large hysteresis and very slow response speeds.
  • polymers such as polyurethane, polybutadine etc. which can generate high electric field induced strain i.e. up to 6-11%.
  • the capacitor industry also requires a capacitor which has a much higher electric energy density than is currently available.
  • Current dielectric materials such as polymers, have a low dielectric constant (-2-10) and 5 limited energy density.
  • the maximum field which can be applied is limited.
  • compositions for electrical or electomechanical devices are achieved by compositions for electrical or electomechanical devices.
  • the present invention provides polymers prepared by a polymerizing a mixture of three monomers comprising: at least one monomer of vinylidene-fluoride; at least one monomer selected from the group consisting of trifluorethylene and tetrafluoroethylene; and at least one monomer selected from the group consisting of tetrafluorethylene, vinyl fluoride, perfluoro (methyl vinyl ether); bromotrifluoroethylene, chlorofluoroethylene, chlorotrifluoroethylene, and hexafluoroethylene.
  • Polymers of the invention exhibit an electrostrictive strain, at room temperature, of 3% or more when an electric field gradient of 100 megavolts per meter or greater is applied thereacross, exhibit a dielectric constant, at room temperature, of 40 or higher at 1 kHz, and exhibit an elastic energy density, at room temperature, of 0.3 joules/cm 3 or higher, or any combinations thereof.
  • the present invention also provides a process for the preparation of polymers comprising: polymerizing a mixture of three monomers comprising at least one monomer of vinylidene-fluoride; at least one monomer selected from the group consisting of trifluorethylene and tetrafluoroethylene; and at least one monomer selected from the group consisting of tetrafluorethylene, vinyl fluoride, perfluoro (methyl vinyl ether), bromotrifluoroethylene, chlorofluoroethylene, chlorotrifluoroethylene, and hexafluoroethylene; stretching said polymer greater than its original length; and thereafter annealing said polymer at a temperature below its melting point, wherein said polymer exhibits an electrostrictive strain, at room temperature, of 3% or more when an electric field gradient of 100 megavolts per meter or greater is applied thereacross, exhibits a dielectric constant, at room temperature, of 40 or higher at 1 kHz, and exhibits an elastic energy density, at room temperature, of 0.3 joules/cm
  • Polymers include, but are not necessarily limited to, polyvinylidene fluoride-trifluorethylene- chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride- trifluoroethylene-chlorotrifluoroethylene P(VDF-TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene-chlorotrifluoroethylene, polyvinylidene fluoride- trifluorethylene-hexafluoroethylene , polyvinylidene fluoride- tetrafluorethylene-hexafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-tetrafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-tetrafluoroethylene
  • Fig. 1 is a graph of electric field induced logitudinal strain as a function of the applied field amplitude for the terpolymer P(VDF-TrFE-CTFE).
  • the terpolymer No. 49 is 72.2/17.8/10 mol %; the terpolymer No. 52 is 66/22.5/11.5 mol %; and the third embodiment of the graph is the terpolymer 58.5/31.5/10 mol%. All measurements were made at room temperature.
  • Fig. 2 is a graph of the field induced transverse strain as a function of the applied field amplitude for the uniaxially stretched terpolymer P(VDF-TrFE-CTFE), 63.1/25.4/11.5 mol% measured at room temperature.
  • Fig. 3 is a graph of the strain hysteresis loop for the terpolymer P(VDF- 0 TrFE-CTFE), 58.5/31.5/10 mol%.
  • Fig. 4a and Fig 4b are graphs of the dialectric constant and loss, respectively, as a function of temperature of the terpolymer P(VDF-TrFE-CTFE) in the frequency range from 100 Hz to 1 MHz (dielectric constant: from the top to 5 bottom: 100, 300, 1k, 3k, 10k, 30k, 100k, 300k, and 1MHz) (dielectric loss: from the bottom to top: 100, 300, 1k, 3k, 10k, 30k, 100k, 300k, and 1MHz).
  • Fig. 5. Is a graph of the field induced longitudinal strain as a function of the applied field amplitude for the terpolymer P(VDF-TrFE-CFE) , 60/36/4 mol% 0 measured at room temperature.
  • the terpolymer is mechanically stretched (4 to 5 times of the original o length) and annealed afterwards at a temperature 5 to 15 degrees below the melting temperature of the polymer, a large field induced transverse strain ( ⁇ 3%), see Fig. 2, can be obtained. Electrostrictive strains of about 3% or above are preferred.
  • the terpolymer has an elastic modulus at room temperature of 0.5 GPa, which results in an elastic energy density (per unit volume) - 0.4 J/cm 3 .
  • Preferred elastic energy densities of terpolymers of the invention are -0.3 J/cm 3 or above. Such a large strain with a very low hysteresis (see Fig. 3) is very useful for electromechanical devices.
  • the P(VDF-TrFE-CTFE) terpolymer has a very high room temperature dielectric constant (c.f., Fig. 4), at 100 Hz, the room temperature dielectric constant can be more that 65, which is significantly higher than any commercial polymers. Dielectric constants of the terpolymers of the invention are preferably 40 or above.
  • composition of the terpolymer P(VDF x -TrFE y - CTFE ⁇ -x -y) should be: x is in the range of 0.55 -0.75 and y in the range of 0.15- 0.35.
  • the present invention discloses a series of terpolymer systems which preferably exhibit high electric field induced strain with high elastic energy density and also high room temperature dielectric constant.
  • the terpolymer systems include poly(vinylidene fluoride-trifluorethylene-chlorofluoroethylene), poly(vinylidene fluoride-trifluorethylene-vinylidene chloride), poly(vinylidene fluoride-trifluorethylene-tetrafluoroethylene), poly(vinylidene fluoride- trifluorethylene-vinyl fluoride), poly(vinylidene fluoride-trifluorethylene- perfluoro(Methyl vinyl ether)), poly(vinylidene fluoride-trifluorethylene- bromotrifluoroethylene), poly(vinylidene fluoride-trifluorethylene- 5 chlorofluoroethylene), and poly(vinylidene fluoride-trifluorethylene-vinylidene chloride).
  • High strain and high dielectric constant polymer systems high energy irradiated P(VDF-TrFE) copolymers, have been earlier disclosed.
  • An advantage of 0 the current terpolymer systems is that the irradiation step used with the copolymer systems is eliminated. This saves manufacture cost and improves the reliability and reproducibility of the electroactive polymer systems.
  • Polymers of the present invention are conveniently prepared or 5 synthesized by polymerizing processing known in the art, such as suspension, emulsion, or solutions methods. Three monomers (i.e., VDF. TrFE, CFE) are selected and contacted or mixed in proportion in the presence of a suitable catalyst or initiator.
  • the resultant terpolymer systems should have a convenient molecular weight suitable for use in electrical or electromechanical devices.
  • the o molecular weight of the polymer systems of the present invention is not limited.
  • the molecular weight of terpolymers is preferably, but not limited to, higher than about 50,000, more preferably higher than 100,000, and yet more preferably from about 100,000 to about 300,000.

Abstract

There are disclosed new polymer materials having improved electric field induced strain levels, dielectric constants, and elastic energy densities for use in electromechanical and dielectric applications. Methods of manufacture of new polymer materials are also disclosed.

Description

TERPOLYMER SYSTEMS FOR ELECTROMECHANICAL AND DIELECTRIC
APPLICATIONS
BACKGROUND OF THE INVENTION
Field of the Invention
The present invention relates to polymeric materials with elevated electric field induced strain levels, elevated elastic energy densities, and having elevated dielectric constants at room temperature. The material can be used in electromechanical devices which convert electric energy into mechanical energy or convert mechanical energy into electric energy. Material of the invention can also be used as a capacitor which stores electric energy and regulates electric voltage in a circuit.
Description of the Prior Art
Both polymers and inorganic materials (such as ceramics) have been used widely in electromechanical devices such as actuators, transducers, artificial muscles and robots. However, in the currently available commercial materials, the strain level and elastic energy density both are quite low (strain ~ 0.1% and elastic density ~ 0.1 J/cm3), which causes many problems for device performance. For example, in order to generate large actuation, in many current devices, an amplification scheme has to be used. In addition, the low elastic energy density also reduces the force and power output of the electromechanical devices. In order to improve the performance of a wide variety of electromechanical devices, it is required that the electric field induced strain level and elastic energy density be improved.
Polymers are also used widely in capacitors for high voltage operation and charge storage. However, the dielectric constant of the current commercial polymers is quite low (below 10). A high dielectric constant polymer can reduce the capacity volume and charge storage capability of the capacity. In spite of their advantages over the ceramics, current polymers suffer low field sensitivities, such as dielectric constant, piezoelectric coefficient, electromechanical coupling factor and field induced strain. 5 These constraints severely limit the application of ferroelectric polymers as transducers, sensors and actuators.
There is a demand for improved materials for use in actuators and transducers due to the limitations of currently available materials. For 0 example, current actuator materials, such as electrostatic, electromagnetic and piezoelectric materials, exhibit limitations in one or more of the following performance parameters: strain, elastic energy density, speed of response and efficiency. For instance, piezoceramic and magnetostrictive materials, while possessing low hysteresis and high response speeds, 5 suffer from low strain levels (-0.1 %). Shape memory alloys generate high strain and high force but are often associated with large hysteresis and very slow response speeds. On the other hand, there are several polymers such as polyurethane, polybutadine etc. which can generate high electric field induced strain i.e. up to 6-11%. But, due to their low elastic modulus, o their elastic energy density is very low. Further, the strain generated in these materials is mainly due to the electrostatic effect, which is a low frequency process. Use of these materials at high frequencies reduces their response drastically. In addition, due to their low dielectric constant, the electric energy density of these polymers is very low which is an 5 undesirable characteristic for many transducer and actuator applications.
Substantial efforts have been devoted to improvement of phase switching materials where an antiferroelectric and ferroelectric phase change can be field induced to cause a high strain in the material. While o strains higher than 0.7% have been achieved in such materials, due to the brittleness of ceramics, severe fatigue has been found to occur at high strain levels. Recently, in a single crystal ferroelectric relaxor, i.e., PZN-PT, an electric field strain of about 1.7%, with very little hysteresis, has been reported, which is exceptionally high for an inorganic materials (see: Park and Shrout, J Appl. Phys., 82, 1804 (1997)). In such ceramic materials, mechanical fatigue occurs at high strain levels, a major obstacle limiting their use for many applications.
5
For many applications, such as microrobots, artificial muscles, vibration controllers, etc., higher strain levels and higher energy densities are required. Thus, there is a need for a general purpose electroactive material with improved performance for use with transducer and actuators. 0
There is a further requirement for improved ultrasonic transducers and sensors for use in medical imaging applications and low frequency acoustic transducers. Current piezoceramic transducer materials, such as PZTs, have a large acoustic impedance (Z>35 Mrayls) mismatch with the 5 air and human tissue (Z<2 Mrayls). On the other hand, piezoelectric polymers such as P(VDF-TrFE), PVDF not only have an acoustic impedance well matched (Z < 4 Mrayls) to human tissue but also offer a broad nonresonant frequency bandwidth. But, because of their low piezoelectric activity and low coupling coefficient, the sensitivity of such o ultrasonic polymer transducers is very low.
The capacitor industry also requires a capacitor which has a much higher electric energy density than is currently available. Current dielectric materials, such as polymers, have a low dielectric constant (-2-10) and 5 limited energy density. In addition, with current ceramics, the maximum field which can be applied is limited.
Accordingly, it is an object of the invention to provide a polymeric material which can generate a high electric field- induced strain with little o hysteresis.
It is another object of the invention to provide a polymeric material which exhibits a high elastic energy density. It is yet another object of the invention to provide a polymeric material that exhibits a room temperature dielectric constant that is higher than other currently available polymers.
These and other objects and advantages of the present invention and equivalents thereof, are achieved by compositions for electrical or electomechanical devices.
SUMMARY OF THE INVENTION
The present invention provides polymers prepared by a polymerizing a mixture of three monomers comprising: at least one monomer of vinylidene-fluoride; at least one monomer selected from the group consisting of trifluorethylene and tetrafluoroethylene; and at least one monomer selected from the group consisting of tetrafluorethylene, vinyl fluoride, perfluoro (methyl vinyl ether); bromotrifluoroethylene, chlorofluoroethylene, chlorotrifluoroethylene, and hexafluoroethylene. Polymers of the invention exhibit an electrostrictive strain, at room temperature, of 3% or more when an electric field gradient of 100 megavolts per meter or greater is applied thereacross, exhibit a dielectric constant, at room temperature, of 40 or higher at 1 kHz, and exhibit an elastic energy density, at room temperature, of 0.3 joules/cm3 or higher, or any combinations thereof.
The present invention also provides a process for the preparation of polymers comprising: polymerizing a mixture of three monomers comprising at least one monomer of vinylidene-fluoride; at least one monomer selected from the group consisting of trifluorethylene and tetrafluoroethylene; and at least one monomer selected from the group consisting of tetrafluorethylene, vinyl fluoride, perfluoro (methyl vinyl ether), bromotrifluoroethylene, chlorofluoroethylene, chlorotrifluoroethylene, and hexafluoroethylene; stretching said polymer greater than its original length; and thereafter annealing said polymer at a temperature below its melting point, wherein said polymer exhibits an electrostrictive strain, at room temperature, of 3% or more when an electric field gradient of 100 megavolts per meter or greater is applied thereacross, exhibits a dielectric constant, at room temperature, of 40 or higher at 1 kHz, and exhibits an elastic energy density, at room temperature, of 0.3 joules/cm3 or higher, or any combinations thereof.
Also provided are electrical or electromechanical devices comprising at least one layer of a polymer of the invention. Polymers include, but are not necessarily limited to, polyvinylidene fluoride-trifluorethylene- chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride- trifluoroethylene-chlorotrifluoroethylene P(VDF-TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene-chlorotrifluoroethylene, polyvinylidene fluoride- trifluorethylene-hexafluoroethylene , polyvinylidene fluoride- tetrafluorethylene-hexafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-tetrafluoroethylene, polyvinylidene fluoride- trifluorethylene-vinyl fluoride, polyvinylidene fluoride-tetrafluorethylene-vinyl fluoride, polyvinylidene fluoride-trifluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-tetrafluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-trifluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-chlorofluoroethylene, polyvinylidene fluoride-trifluorethylene-vinylidene chloride, and polyvinylidene fluoride-tetrafluorethylene-vinylidene chloride
BRIEF DESCRIPTION OF THE DRAWINGS
Fig. 1 is a graph of electric field induced logitudinal strain as a function of the applied field amplitude for the terpolymer P(VDF-TrFE-CTFE). The terpolymer No. 49 is 72.2/17.8/10 mol %; the terpolymer No. 52 is 66/22.5/11.5 mol %; and the third embodiment of the graph is the terpolymer 58.5/31.5/10 mol%. All measurements were made at room temperature.
5 Fig. 2 is a graph of the field induced transverse strain as a function of the applied field amplitude for the uniaxially stretched terpolymer P(VDF-TrFE-CTFE), 63.1/25.4/11.5 mol% measured at room temperature.
Fig. 3 is a graph of the strain hysteresis loop for the terpolymer P(VDF- 0 TrFE-CTFE), 58.5/31.5/10 mol%.
Fig. 4a and Fig 4b are graphs of the dialectric constant and loss, respectively, as a function of temperature of the terpolymer P(VDF-TrFE-CTFE) in the frequency range from 100 Hz to 1 MHz (dielectric constant: from the top to 5 bottom: 100, 300, 1k, 3k, 10k, 30k, 100k, 300k, and 1MHz) (dielectric loss: from the bottom to top: 100, 300, 1k, 3k, 10k, 30k, 100k, 300k, and 1MHz).
Fig. 5. Is a graph of the field induced longitudinal strain as a function of the applied field amplitude for the terpolymer P(VDF-TrFE-CFE) , 60/36/4 mol% 0 measured at room temperature.
DETAILED DESCRIPTION OF THE INVENTION
It was found that in certain classes of terpolymer systems such as P(VDF- 5 TrFE-CTFE) (poly(vinylidene fluoride-trifluorethylene-chlorotrifluoroethylene)) and P(VDF-TrFE-CFE) (poly(vinylidene fluoride-trifluorethylene- chlorofluoroethylene)), an ultrahigh electric field induced strain can be achieved. In P(VDF-TrFE-CTFE), as shown in Fig. 1 , a thickness strain of -4% can be induced. If the terpolymer is mechanically stretched (4 to 5 times of the original o length) and annealed afterwards at a temperature 5 to 15 degrees below the melting temperature of the polymer, a large field induced transverse strain (~ 3%), see Fig. 2, can be obtained. Electrostrictive strains of about 3% or above are preferred. In addition, the terpolymer has an elastic modulus at room temperature of 0.5 GPa, which results in an elastic energy density (per unit volume) - 0.4 J/cm3. Preferred elastic energy densities of terpolymers of the invention are -0.3 J/cm3 or above. Such a large strain with a very low hysteresis (see Fig. 3) is very useful for electromechanical devices.
It was also found that the P(VDF-TrFE-CTFE) terpolymer has a very high room temperature dielectric constant (c.f., Fig. 4), at 100 Hz, the room temperature dielectric constant can be more that 65, which is significantly higher than any commercial polymers. Dielectric constants of the terpolymers of the invention are preferably 40 or above.
For those applications, the composition of the terpolymer P(VDFx-TrFEy- CTFEι-x-y) should be: x is in the range of 0.55 -0.75 and y in the range of 0.15- 0.35.
In P(VDF-TrFE-CFE) terpolymer system, as shown in Fig. 5, there is also a large thickness strain induced electrically. In this terpolymer (60/36/4 mol%, P(VDFx-TrFEy-CFEι-x-y)), a relatively high thickness strain (-4.5%) can be induced under a field -150 MV/m The terpolymer also exhibits a high elastic modulus ~ 1 GPa which results in an elastic energy density - 1 J/cm3, much higher than those in the piezoelectric materials. For this terpolymer system, the composition range of P(VDFχ-TrFEy-CFEι.χ.y), x should be in the range of 0.55 - 0.8 and y in the range of 0.15 - 0.4.
The high strain and high elastic energy density discovered in the terpolymer systems here are very attractive because it is well known that polymers can withstand high elastic strains without fatigue. This is a clear advantage over any inorganic material where the fatigue at high mechanical strain is a serious problem for the electromechanical device applications.
The present invention discloses a series of terpolymer systems which preferably exhibit high electric field induced strain with high elastic energy density and also high room temperature dielectric constant. The terpolymer systems include poly(vinylidene fluoride-trifluorethylene-chlorofluoroethylene), poly(vinylidene fluoride-trifluorethylene-vinylidene chloride), poly(vinylidene fluoride-trifluorethylene-tetrafluoroethylene), poly(vinylidene fluoride- trifluorethylene-vinyl fluoride), poly(vinylidene fluoride-trifluorethylene- perfluoro(Methyl vinyl ether)), poly(vinylidene fluoride-trifluorethylene- bromotrifluoroethylene), poly(vinylidene fluoride-trifluorethylene- 5 chlorofluoroethylene), and poly(vinylidene fluoride-trifluorethylene-vinylidene chloride).
High strain and high dielectric constant polymer systems, high energy irradiated P(VDF-TrFE) copolymers, have been earlier disclosed. An advantage of 0 the current terpolymer systems is that the irradiation step used with the copolymer systems is eliminated. This saves manufacture cost and improves the reliability and reproducibility of the electroactive polymer systems.
Polymers of the present invention are conveniently prepared or 5 synthesized by polymerizing processing known in the art, such as suspension, emulsion, or solutions methods. Three monomers ( i.e., VDF. TrFE, CFE) are selected and contacted or mixed in proportion in the presence of a suitable catalyst or initiator. The resultant terpolymer systems should have a convenient molecular weight suitable for use in electrical or electromechanical devices. The o molecular weight of the polymer systems of the present invention is not limited.
The molecular weight of terpolymers is preferably, but not limited to, higher than about 50,000, more preferably higher than 100,000, and yet more preferably from about 100,000 to about 300,000.
5
Although the present invention describes in detail certain embodiments, it is understood that variations and modifications exist known to those skilled in the art that are within the invention. Accordingly, the present invention is intended to encompass all such alternatives, modifications and o variations that are within the scope of the invention as set forth in the following claims.

Claims

WHAT IS CLAIMED IS:
1. A polymer prepared by a polymerizing a mixture of three monomers comprising:
0 at least one monomer of vinylidene-fluoride;
at least one monomer selected from the group consisting of trifluorethylene and tetrafluoroethylene; and
5 at least one monomer selected from the group consisting of tetrafluorethylene; vinyl fluoride; perfluoro (methyl vinyl ether); bromotrifluoroethylene; chlorofluoroethylene; chlorotrifluoroethylene; and hexafluoroethylene.
0 2. The polymer of claim 1 , wherein said polymer is selected from the group consisting of polyvinylidene fluoride-trifluorethylene- chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride- trifluoroethylene-chlorotrifluoroethylene P(VDF-TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene-chlorotrifluoroethylene, polyvinylidene fluoride- 5 trifluorethylene-hexafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-hexafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-tetrafluoroethylene, polyvinylidene fluoride- trifluorethylene-vinyl fluoride, polyvinylidene fluoride-tetrafluorethylene-vinyl o fluoride, polyvinylidene fluoride-trifluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-tetrafluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-trifluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-chlorofluoroethylene, polyvinylidene fluoride-trifluorethylene-vinylidene chloride, and polyvinylidene fluoride-tetrafluorethylene-vinylidene chloride.
3. The polymer of claim 1 , wherein said polymer is polyvinylidene fluoride-trifluoroethylene-chlorotrifluoroethylene having a ratio of monomers represented as P(VDFx-TrFEy-CTFEι.x.y), wherein x is about 0.55 to about 0.75, y is about 0.15 to about 0.35.
4. The polymer of claim 1 , wherein said polymer is polyvinylidene fluoride-trifluorethylene-hexafluoroethylene having a ratio of monomers represented as P(VDFx-TrFEy-HFPι-x-y), wherein x is about 0.55 to about 0.75, and y is about 0.15 to about 0.4.
5. A polymer of claim 1 , wherein said polymer exhibits an electrostrictive strain, at room temperature, of 3% or more when an electric field gradient of 100 megavolts per meter or greater is applied thereacross.
6. The polymer of claim 5, wherein said polymer is selected from the group consisting of polyvinylidene fluoride-trifluorethylene- chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride- trifluoroethylene-chlorotrifluoroethylene P(VDF-TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene-chlorotrifluoroethylene, polyvinylidene fluoride- trifluorethylene-hexafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-hexafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-tetrafluoroethylene, polyvinylidene fluoride- trifluorethylene-vinyl fluoride, polyvinylidene fluoride-tetrafluorethylene-vinyl fluoride, polyvinylidene fluoride-trifluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-tetrafluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-trifluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-chlorofluoroethylene, polyvinylidene fluoride-trifluorethylene-vinylidene chloride, and polyvinylidene fluoride-tetrafluorethylene-vinylidene chloride.
7. A polymer of claim 1 , wherein said polymer exhibits a dielectric constant, at room temperature, of 40 or higher at 1 kHz.
8. The polymer of claim 7, wherein said polymer is selected from the group consisting of polyvinylidene fluoride-trifluorethylene- chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride- 0 trifluoroethylene-chlorotrifluoroethylene P(VDF-TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene-chlorotrifluoroethylene, polyvinylidene fluoride- trifluorethylene-hexafluoroethylene , polyvinylidene fluoride- tetrafluorethylene-hexafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- 5 tetrafluorethylene-tetrafluoroethylene, polyvinylidene fluoride- trifluorethylene-vinyl fluoride, polyvinylidene fluoride-tetrafluorethylene-vinyl fluoride, polyvinylidene fluoride-trifluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-tetrafluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-trifluorethylene-bromotrifluoroethylene, o polyvinylidene fluoride-tetrafluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-chlorofluoroethylene, polyvinylidene fluoride-trifluorethylene-vinylidene chloride, and polyvinylidene fluoride-tetrafluorethylene-vinylidene chloride.
5 9. A polymer of claim 1 , wherein said polymer exhibits an elastic energy density, at room temperature, of 0.3 joules/cm3 or higher.
10. The polymer of claim 8, wherein said polymer is selected from the group consisting of polyvinylidene fluoride-trifluorethylene- 0 chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride- trifluoroethylene-chlorotrifluoroethylene P(VDF-TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene-chlorotrifluoroethylene, polyvinylidene fluoride- trifluorethylene-hexafluoroethylene , polyvinylidene fluoride- tetrafluorethylene-hexafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-tetrafluoroethylene, polyvinylidene fluoride- trifluorethylene-vinyl fluoride, polyvinylidene fluoride-tetrafluorethylene-vinyl fluoride, polyvinylidene fluoride-trifluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-tetrafluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-trifluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-chlorofluoroethylene, 0 polyvinylidene fluoride-trifluorethylene-vinylidene chloride, and polyvinylidene fluoride-tetrafluorethylene-vinylidene chloride.
11. An electrical or electromechanical device comprising at least one layer of a polymer of claim 1. 5
12. The electrical or electromechanical device of claim 11 , wherein Said polymer is selected from the group consisting of polyvinylidene fluoride-trifluorethylene-chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride-trifluoroethylene-chlorotrifluoroethylene P(VDF- 0 TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene- chlorotrifluoroethylene, polyvinylidene fluoride-trifluorethylene- hexafluoroethylene , polyvinylidene fluoride-tetrafluorethylene- hexafluoroethylene, polyvinylidene fluoride-trifluorethylene- tetrafluoroethylene, polyvinylidene fluoride-tetrafluorethylene- 5 tetrafluoroethylene, polyvinylidene fluoride-trifluorethylene-vinyl fluoride, polyvinylidene fluoride-tetrafluorethylene-vinyl fluoride, polyvinylidene fluoride-trifluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-tetrafluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-trifluorethylene-bromotrifluoroethylene, polyvinylidene fluoride- o tetrafluorethylene-bromotrifluoroethylene, polyvinylidene fluoride- tetrafluorethylene-chlorofluoroethylene polyvinylidene fluoride- trifluorethylene-vinylidene chloride, and polyvinylidene fluoride- tetrafluorethylene-vinylidene chloride.
13. A process for the preparation of a polymer comprising:
polymerizing a mixture of three monomers comprising at least one monomer of vinylidene-fluoride; at least one monomer selected from the group consisting of trifluorethylene and tetrafluoroethylene; and at least one monomer selected from the group consisting of tetrafluorethylene; vinyl fluoride; perfluoro (methyl vinyl ether); bromotrifluoroethylene; chlorofluoroethylene; chlorotrifluoroethylene; and hexafluoroethylene;
stretching said polymer greater than its original length; and thereafter
annealing said polymer at a temperature below its melting point, wherein said polymer exhibits an electrostrictive strain, at room temperature, of 3% or more when an electric field gradient of 100 megavolts per meter or greater is applied thereacross, exhibits a dielectric constant, at room temperature, of 40 or higher at 1 kHz, and exhibits an elastic energy density, at room temperature, of 0.3 joules/cm3 or higher, or any combinations thereof.
14. The process of claim 13, wherein said polymer is stretched at least four times its original length.
15. The process of claim 13, wherein said polymer is annealed at a temperature of at least 1 ° F below its melting point, preferably from 1° F to 30°F below its melting point, and more preferably from 5° F to 15 ° F below its melting point.
16. The process of claim 13, wherein said polymer is selected from the group consisting of polyvinylidene fluoride-trifluorethylene- chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride- trifluoroethylene-chlorotrifluoroethylene P(VDF-TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene-chlorotrifluoroethylene, polyvinylidene fluoride- trifluorethylene-hexafluoroethylene , polyvinylidene fluoride- tetrafluorethylene-hexafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- 5 tetrafluorethylene-tetrafluoroethylene, polyvinylidene fluoride- trifluorethylene-vinyl fluoride, polyvinylidene fluoride-tetrafluorethylene-vinyl fluoride, polyvinylidene fluoride-trifluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-tetrafluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-trifluorethylene-bromotrifluoroethylene, o polyvinylidene fluoride-tetrafluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-chlorofluoroethylene, polyvinylidene fluoride-trifluorethylene-vinylidene chloride, and polyvinylidene fluoride-tetrafluorethylene-vinylidene chloride.
5 17. A polymer prepared by prepared by a polymerizing a mixture of three monomers comprising:
at least one monomer of vinylidene-fluoride;
0 at least one monomer selected from the group consisting of of trifluorethylene and tetrafluoroethylene; and
at least one monomer selected from the group consisting of tetrafluorethylene; vinyl fluoride; perfluoro (methyl vinyl ether); 5 bromotrifluoroethylene; chlorofluoroethylene; chlorotrifluoroethylene; and hexafluoroethylene, wherein said polymer exhibits an electrostrictive strain, at room temperature, of 3% or more when an electric field gradient of 100 megavolts per meter or greater is applied thereacross, exhibits a dielectric constant, at room temperature, of 40 or higher at 1 kHz, and exhibits an o elastic energy density, at room temperature, of 0.3 joules/cm3 or higher, or any combinations thereof.
18. The polymer of claim 17, wherein said polymer is selected from the group consisting of polyvinylidene fluoride-trifluorethylene- chlorofluoroethylene P(VDF-TrFE-CFE), polyvinylidene fluoride- trifluoroethylene-chlorotrifluoroethylene P(VDF-TrFE-CTFE), polyvinylidene fluoride-tetrafluoroethylene-chlorotrifluoroethylene, polyvinylidene fluoride- trifluorethylene-hexafluoroethylene , polyvinylidene fluoride- tetrafluorethylene-hexafluoroethylene, polyvinylidene fluoride- trifluorethylene-tetrafluoroethylene, polyvinylidene fluoride- tetrafluorethylene-tetrafluoroethylene, polyvinylidene fluoride- trifluorethylene-vinyl fluoride, polyvinylidene fluoride-tetrafluorethylene-vinyl fluoride, polyvinylidene fluoride-trifluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-tetrafluorethylene-perfluoro(methyl vinyl ether), polyvinylidene fluoride-trifluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-bromotrifluoroethylene, polyvinylidene fluoride-tetrafluorethylene-chlorofluoroethylene, polyvinylidene fluoride-trifluorethylene-vinylidene chloride, and polyvinylidene fluoride-tetrafluorethylene-vinylidene chloride.
PCT/US2002/009181 2001-03-30 2002-03-27 Terpolymer systems for electromechanical and dielectric applications WO2002079285A1 (en)

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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1748053A1 (en) * 2005-07-28 2007-01-31 Institut Franco-Allemand de Recherches de Saint-Louis Process for the manufacture of dielectric terpolymer of vinylidene fluoride and trifluoroethylene
CN100406480C (en) * 2006-12-28 2008-07-30 中昊晨光化工研究院 Fluorine elastomer containing high fluorine content and preparation process thereof
US9099410B2 (en) 2003-10-13 2015-08-04 Joseph H. McCain Microelectronic device with integrated energy source
CN108052698A (en) * 2017-11-21 2018-05-18 中国石油大学(华东) A kind of method in Hysteresis Energy density prediction material creep fatigue interaction service life

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4298719A (en) * 1978-07-27 1981-11-03 Kureha Kagaku Kogyo Kabushiki Kaisha Doubly oriented film of polyvinylidene fluoride
US4824911A (en) * 1987-08-21 1989-04-25 Mobil Oil Corporation Blends and molded articles comprising methacrylate polymers and vinylidene fluoride - hexafluoropropylene copolymer
US5356500A (en) * 1992-03-20 1994-10-18 Rutgers, The State University Of New Jersey Piezoelectric laminate films and processes for their manufacture
US6215231B1 (en) * 1998-05-04 2001-04-10 The Penn State Research Foundation Hollow sphere transducers
US6291106B1 (en) * 1998-05-22 2001-09-18 Teijin Limited Electrolytic-solution-supporting polymer film and secondary battery

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4298719A (en) * 1978-07-27 1981-11-03 Kureha Kagaku Kogyo Kabushiki Kaisha Doubly oriented film of polyvinylidene fluoride
US4824911A (en) * 1987-08-21 1989-04-25 Mobil Oil Corporation Blends and molded articles comprising methacrylate polymers and vinylidene fluoride - hexafluoropropylene copolymer
US5356500A (en) * 1992-03-20 1994-10-18 Rutgers, The State University Of New Jersey Piezoelectric laminate films and processes for their manufacture
US6215231B1 (en) * 1998-05-04 2001-04-10 The Penn State Research Foundation Hollow sphere transducers
US6291106B1 (en) * 1998-05-22 2001-09-18 Teijin Limited Electrolytic-solution-supporting polymer film and secondary battery

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9099410B2 (en) 2003-10-13 2015-08-04 Joseph H. McCain Microelectronic device with integrated energy source
US9413405B2 (en) 2003-10-13 2016-08-09 Joseph H. McCain Microelectronic device with integrated energy source
EP1748053A1 (en) * 2005-07-28 2007-01-31 Institut Franco-Allemand de Recherches de Saint-Louis Process for the manufacture of dielectric terpolymer of vinylidene fluoride and trifluoroethylene
FR2889193A1 (en) * 2005-07-28 2007-02-02 Saint Louis Inst PROCESS FOR THE PRODUCTION OF DIELECTRIC TERPOLYMERS BASED ON VINYLIDENE DIFLUORIDE AND TRIFLUOROETHYLENE
US7750098B2 (en) 2005-07-28 2010-07-06 Institut Franco-Allemand De Recherches De Saint-Louis Method of manufacturing vinylidene difluoride and trifluoroethylene-based dielectric copolymers
CN100406480C (en) * 2006-12-28 2008-07-30 中昊晨光化工研究院 Fluorine elastomer containing high fluorine content and preparation process thereof
CN108052698A (en) * 2017-11-21 2018-05-18 中国石油大学(华东) A kind of method in Hysteresis Energy density prediction material creep fatigue interaction service life
CN108052698B (en) * 2017-11-21 2020-12-25 中国石油大学(华东) Method for predicting creep fatigue interaction life of material by hysteresis energy density

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