• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
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    • 专利摘要:
    The invention relates to a composition comprising: - at least one electroactive fluorinated terpolymer, and - at least one second polymer compatible with the electroactive fluorinated terpolymer, and having a glass transition temperature lower than that of the electroactive fluorinated terpolymer. The invention also relates to a method of manufacturing this composition, as well as to a device such as an actuator comprising a substrate and a film of the above composition.
    公开号:FR3031519A1
    申请号:FR1550291
    申请日:2015-01-14
    公开日:2016-07-15
    发明作者:Dos Santos Fabrice Domingues；Thierry Lannuzel；Jean-Fabien Capsal；Pierre-Jean Cottinet；Jeremy Galineau；Minh-Quyen Le
    申请人:Arkema France SA；Institut National des Sciences Appliquees de Lyon ；
    IPC主号:
    专利说明:

    [0001] FIELD OF THE INVENTION The present invention relates to a composition obtained by mixing an electroactive fluorinated terpolymer and a polymer compatible with the electroactive fluorinated terpolymer and having a glass transition temperature lower than that of the terpolymer. electroactive fluoride. The invention also relates to the method of manufacturing this composition.
    [0002] BACKGROUND OF THE INVENTION Fluoropolymers are a class of compounds having outstanding properties for a variety of applications, from paint or specialty coatings to seals, optics, microelectronics and plastics. membrane technology. Among these fluoropolymers, the copolymers are particularly interesting because of their diversity, their morphology, their exceptional properties and their versatility. The electroactive fluorinated terpolymers, generally used in the form of films, deposits or stacks, combined with electrodes, have remarkable electromechanical properties. They have a high density of electromechanical energy. Thus, when devices comprising such terpolymers are subjected to an electric field, they deform, which allows the realization of actuators.
    [0003] US 6,787,238 discloses the preparation of terpolymers according to a method of polymerizing a mixture of three monomers comprising a vinylidene fluoride (VDF) monomer, a monomer such as tetrafluoroethylene (TFE) or trifluoroethylene (TrFE) and a monomer such as tetrafluoroethylene (TFE), vinyl fluoride, perfluoro (methyl vinyl ether), bromotrifluoroethylene, chlorofluoroethylene, chlorotrifluoroethylene (CTFE) and hexafluoropropylene (HFP).
    [0004] US Pat. No. 6,355,479 describes the preparation of terpolymers of vinylidene fluoride, trifluoroethylene and a comonomer such as CTFE or HFP, according to a method of controlled copolymerization using borane compounds. presence of oxygen.
    [0005] US 5,087,679 discloses the preparation of a dielectric terpolymer which comprises vinylidene fluoride, trifluoroethylene and chlorotrifluoroethylene. US 4,554,335 discloses a dielectric polymeric material composed of vinylidene fluoride, ethylene trifluoride, ethylene trifluoride chloride, and another fluorine-containing monomer. High Electromechanical Responses in Poly (vinylidene fluoride-trifluoroethylenechlorofluoroethylene) terpolymer of Xia et al. published in Advanced Materials, 14: 1574-1577 (2002) shows the importance of a third monomer for influencing the microstructure of the vinylidene fluoride and trifluoroethylene copolymer. The article Influencing dielectric properties of a vinylidene fluoride-trifluoroethylene-based terpolymer with a ferroelectric copolymer by Casar et al. in Journal of Applied Physics 115: 104101 (2014) discloses the admixture of a relaxor terpolymer P (VDF-TrFE-CFE) and a ferroelectric polymer P (VDF-TrFE). Similarly, the article A polymer blend approach to tailoring the ferroelectric replies in P (VDF-TrFE) based copolymers, Chen et al. in Polymer 54: 2373-2381 (2013) also describes the mixing of a terpolymer and a copolymer.
    [0006] WO 2011/008940 discloses mixing a terpolymer and another fluoropolymer. EP 0206926 discloses mixtures of fluorinated polymers or copolymers. Finally, WO 2014/170479 discloses mixtures of a P (VDF-TrFE-CFE) or P (VDF-TrFE-CTFE) terpolymer with a phthalate plasticizer, and their use for making films and actuators. . It is disclosed that these mixtures have improved dielectric permittivity. These mixtures, however, have a poor ecotoxicological profile, the phthalate plasticizer used being toxic. Furthermore, the present inventors have found that the phthalate plasticizer has a tendency to release (or oozing), which represents a health risk, makes electrode deposition difficult and can lead to a significant reduction in the mechanical properties of the films. obtained.
    [0007] There is therefore a need to develop a composition having good electromechanical properties (especially for use in actuators), having a satisfactory eco-toxicological profile and having no risk of salting out. . SUMMARY OF THE INVENTION The invention firstly relates to a composition comprising: at least one electroactive fluorinated terpolymer, and at least one second polymer compatible with the electroactive fluorinated terpolymer, and having a glass transition temperature lower than that of the electroactive fluorinated terpolymer. According to one embodiment, the second polymer has a glass transition temperature of at least 5 ° C, preferably at least 10 ° C, or at least 15 ° C, or at least 20 ° C. ° C, to that of the electroactive fluorinated terpolymer. According to one embodiment, the glass transition temperature of the electroactive fluorinated terpolymer is from -50 ° C to + 10 ° C, preferably from 40 ° C to -10 ° C; and / or the glass transition temperature of the second polymer is from -100 ° C to -0 ° C, preferably from -100 ° C to -40 ° C. According to one embodiment, the electroactive fluorinated terpolymer is a terpolymer of vinylidene fluoride, trifluoroethylene and a third monomer. According to one embodiment, the third monomer is chlorofluoro- 1,1-ethylene or chlorotrifluoroethylene. According to one embodiment, the second polymer is a polyester, preferably chosen from polyadipates, polyglutarates and polysébaçates. According to one embodiment, the electroactive fluorinated terpolymer and the second polymer are present in a weight ratio of 50:50 to 99: 1, preferably 70:30 to 95: 5, more preferably 80:20. at 90:10. According to one embodiment, the composition comprises at least one solvent, preferably chosen from tetrahydrofuran, methyl ethyl ketone, dimethylformamide, dimethylacetamide, tetramethylurea, dimethylsulfoxide, trimethylphosphate and N-methyl-2-pyrrolidone. acetone, methyl isobutyl ketone, glycol ethers, glycol ether esters, N-butyl acetate, cyclohexanone, diacetone alcohol, diisobutyl ketone, ethyl acetoacetate, butyrolactone, isophorone, triethylphosphate, carbitol acetate, propylene carbonate and glyceryl triacetate. According to one embodiment: the electroactive fluorinated terpolymer has a molecular weight of from 200,000 to 1,500,000, preferably from 250,000 to 1,000,000, more particularly from 300,000 to 700,000; and / or the second polymer has a molecular weight of from 500 to 700,000, preferably from 2,000 to 100,000, and more preferably from 5,000 to 20,000. According to one embodiment, the composition also comprises a fluorinated copolymer , in particular ferroelectric, preferably chosen from copolymers of vinylidene fluoride and trifluoroethylene, vinylidene fluoride and chlorotrifluoroethylene, vinylidene fluoride and tetrafluoroethylene, and vinylidene fluoride and hexafluoropropylene. The invention also relates to a method of manufacturing a composition as described above, comprising a step of mixing the electroactive fluorinated terpolymer with the second polymer. According to one embodiment, the mixture is carried out in a solvent, preferably chosen from tetrahydrofuran, methyl ethyl ketone, dimethylformamide, dimethylacetamide, tetramethylurea, dimethylsulfoxide, trimethylphosphate and N-methyl-2-pyrrolidone. acetone, methyl isobutyl ketone, glycol ethers, glycol ether esters, N-butyl acetate, cyclohexanone, diacetone alcohol, diisobutyl ketone, ethyl acetoacetate, butyrolactone, isophorone triethylphosphate, carbitol acetate, propylene carbonate and glyceryl triacetate; preferably by dissolving the electroactive fluorinated terpolymer and then the second polymer in the solvent. The invention also relates to a device comprising a substrate, and a film of the composition described above disposed thereon. According to one embodiment, the device further comprises electrodes on either side of the film, said device preferably being an actuator. The invention also relates to a method of manufacturing the device 35 above, comprising a step of depositing the film on the substrate. According to one embodiment, the deposition step is a step of coating or printing the composition on the substrate.
    [0008] According to one embodiment, the manufacturing method comprises an additional step of electrode deposition, preferably by evaporation or sputtering of metal, indium-tin oxide, a conductive polymer layer, conductive ink. based on silver, silver nanowires, or graphene. The present invention overcomes the disadvantages of the state of the art. It provides more particularly a composition having good electromechanical properties (especially for use in actuators), having a satisfactory eco-toxicological profile and having no risk of salting out. This is accomplished by the combination of an electroactive fluorinated terpolymer and a second terpolymer-compatible polymer having a lower glass transition temperature than the terpolymer.
    [0009] The present inventors have found that this combination provides considerably improved electromechanical properties (higher deformation in the electric field, extended electromechanical properties over a wide temperature range) than those of the terpolymer alone, while avoiding the problems of toxicity or salting out encountered when phthalate plasticizers are used. The mechanical properties (in particular the modulus of elasticity) are not impaired either, compared to the terpolymers alone. In particular, the composition of the invention offers an ease of implementation, in particular during the manufacture of films or multilayer deposits, because of the absence of release of compound. It is particularly suitable for the manufacture of actuators. DESCRIPTION OF EMBODIMENTS OF THE INVENTION The invention is now described in more detail and in a nonlimiting manner in the description which follows. The invention is based firstly on the use of an electroactive fluorinated terpolymer. By "fluorinated" is meant a terpolymer having -F groups. By "electroactive" is meant a terpolymer capable of deforming under the effect of an electric field.
    [0010] Preferably, the fluorinated terpolymer is a relaxor ferroelectric polymer. Such a material has a low coercive field (typically less than 10 V / pm) and a low remanent polarization (typically less than 10 mC / m 2) or even zero.
    [0011] Preferably, the terpolymer comprises units of vinylidene fluoride. More preferably, the terpolymer is of formula P (VDF-TrFE-X), wherein VDF is vinylidene fluoride units, TrFE is trifluoroethylene units, and X is units derived from a third monomer, preferably a third fluorinated monomer. More preferably, X represents units derived from CFE (1-chloro-1-fluoroethylene) or CTFE (chlorotrifluoroethylene). Alternatively, the monomeric third may in particular be chosen from halogenated alkenes, especially halogenated propenes or ethenes, and for example from tetrafluoropropenes (in particular 2,3,3,3-tetrafluoropropene) and chlorotrifluoropropenes (especially 2-chloro-3). 3,3-trifluoropropene), 1-chloro-2-fluoroethylene, trifluoropropenes (especially 3,3,3-trifluoropropene), pentafluoropropenes (especially 1,1,3,3,3-pentafluoropropene or 1,2,3,3,3-pentafluoropropene), 1-chloro-2,2-difluoroethylene, 1-chloro, 2-fluoroethylene, 1-bromo-2,2-difluoroethylene, bromotrifluoroethylene, fluoroethylene ( or vinyl fluoride), tetrafluoroethylene and hexafluoropropene. The third monomer may also be a perfluoroalkylvinylether, of the general formula RrO-CF-CF2, Rf being an alkyl group, preferably a C1 to C4 group. Preferred examples are PPVE (perfluoropropylvinylether) and PMVE (perfluoromethylvinylether). The terpolymers of the invention may be produced using any known method, such as emulsion polymerization, suspension polymerization and solution polymerization. The use of the method described in WO 2010/116105 is particularly preferred. This process makes it possible to obtain polymers of high molecular weight and suitable structuring. According to one embodiment, the molar proportion of X units in the terpolymer is 2 to 15%, preferably 3 to 12%, and more preferably 5 to 10%. According to one embodiment, the molar ratio of the VDF units on the TrFE units in the terpolymer is 80/20 to 50/50, and preferably 72/28 to 60/40.
    [0012] According to one embodiment, the weight average molecular weight (MW) of the terpolymer is from 200,000 to 1,500,000, preferably from 250,000 to 1,000,000, and more preferably from 300,000 to 700,000.
    [0013] The latter can be adjusted by modifying certain process parameters, such as the temperature in the reactor, or by adding a transfer agent. The molecular weight distribution can be estimated by SEC (size exclusion chromatography) with dimethylformamide (DMF) as eluent, with a set of 3 columns of increasing porosity. The stationary phase is a styrene-DVB gel. The detection method is based on a measurement of the refractive index, and the calibration is performed with polystyrene standards. The sample is dissolved in 0.5 g / L in DMF and filtered through a 0.45 μm nylon filter. The molecular weight can also be evaluated by measuring the melt index at 230 ° C. under a load of 5 kg according to ASTM D1238 (ISO 1133). On the other hand, the molecular weight can also be characterized by measuring the solution viscosity according to ISO 1628. Methyl ethyl ketone (MEK) is a preferred solvent for terpolymers for viscosity index determination. More generally, the molar composition of the terpolymers of the invention can be determined by various means. The standard methods of elemental analysis in carbon, fluorine and chlorine or bromine elements lead to a system of two or three independent equations with two independent unknowns (for example% VDF and% TrFE, with% X = 100 (% VDF +% TrFE)), which makes it possible to calculate without ambiguity the mass composition of the polymers, from which the molar composition is deduced.
    [0014] The multi-core NMR techniques, proton (1H) and fluorine (19F), can also be carried out by analyzing a solution of the polymer in a suitable deuterated solvent. The NMR spectrum is recorded on an FT-NMR spectrometer equipped with a multi-nuclear probe. The specific signals given by the various monomers are then identified in the spectra produced according to one or the other nuclei. Thus, for example, the TrFE unit (CFH = CF2) gives proton NMR a specific signal characteristic of the CFH group (at about 5 ppm). It is the same for CH2 groups of VDF (massive centered at 3 ppm). The relative integration of the two signals gives the relative abundance of the two monomers, i.e. the VDF / TrFE molar ratio. The combination of the relative integrations of the different signals obtained by proton NMR and by fluorine NMR leads to a system of equations whose resolution leads to obtaining the molar concentrations of the different monomeric units. Finally, it is possible to combine elemental analysis, for example for heteroatoms such as chlorine or bromine, and NMR analysis. It is thus that the content of CTFE or CFE can be determined by a measurement of the chlorine content by elemental analysis. Those skilled in the art thus have a range of methods or combination of methods enabling them to determine without ambiguity and with the necessary precision the composition of the terpolymers of the invention.
    [0015] The invention is then based on the use of a second polymer compatible with the terpolymer and having a glass transition temperature lower than that of the terpolymer. By "compatible" is meant that the mixture of the two polymers forms a homogeneous phase with a single glass transition temperature. The glass transition temperature of the polymers of the invention can be measured by differential scanning calorimetry, for example according to ASTM E1356. Thus, preferably the glass transition temperature of the second polymer is at least 5 ° C, or at least 10 ° C, or at least 15 ° C, or at least 20 ° C, at the glass transition temperature of the terpolymer. According to one embodiment, the glass transition temperature of the terpolymer may be from 10 to -50 ° C, preferably from 0 to -40 ° C and more preferably from -10 to -40 ° C (e.g. ° C). According to one embodiment, the glass transition temperature of the second polymer may be less than -20 ° C, preferably less than -30 ° C and more particularly less than -40 ° C. For example, it can be from -100 ° C to -0 ° C, preferably from -100 ° C to -40 ° C.
    [0016] Preferably, the second polymer is not fluorinated. Preferably, the second polymer is not a ferroelectric polymer. Preferably, the second polymer is not an electroactive polymer.
    [0017] Preferably, the second polymer is a polar polymer. Preferably, the second polymer is a non-crystalline polymer. Polymers for which a differential scanning calorimetry measurement reveals an endothermic phenomenon comparable to an enthalpy melting of less than 5 J / g are non-crystalline polymers. The second polymer may in particular be a polyester. Preferably it is a polyadipate, a polyglutarate or a polysébaçate.
    [0018] The molecular weight of the second polymer is preferably greater than or equal to 500, or to 2000 or 5000. It is preferably less than or equal to 700000, and more particularly less than or equal to 20000. The composition of the invention comprises at least minus a terpolymer as described above (optionally two or more thereof), and at least one second polymer as described above (optionally two or more thereof). This composition may also comprise a solvent (in which case it may be a composition adapted to be deposited on a substrate for example). Alternatively, it may be devoid of solvent (such a composition may for example be obtained from the previous one by evaporation of the solvent, for example after deposition on a substrate). As a suitable solvent, there may be used tetrahydrofuran, methyl ethyl ketone, dimethylformamide, dimethylacetamide, tetramethylurea, dimethylsulfoxide, trimethylphosphate, N-methyl-2-pyrrolidone, acetone, methyl isobutyl ketone, glycol ethers, glycol ether esters, N-butyl acetate, cyclohexanone, diacetone alcohol, diisobutyl ketone, ethyl acetoacetate, butyrolactone, isophorone, triethylphosphate, carbitol acetate propylene carbonate and glyceryl triacetate.
    [0019] The composition of the invention may also comprise one or more additional polymers, such as ferroelectric fluorinated copolymers (for example P (VDF-TrFE)) or not (for example P (VDFCTFE), P (VDF-HFP)) . The composition of the invention may also comprise one or more additives, especially chosen from plasticizers, salts and flame retardants. Preferably, the composition according to the invention is free of phthalate compound. The electroactive fluorinated terpolymer and the second polymer are advantageously present in a mass ratio terpolymer: second polymer of 50:50 to 99: 1, preferably 70:30 to 95: 5, more preferably 80:20 to 90:10.
    [0020] When the composition comprises a solvent, it may preferably be present in a mass proportion of at least 50%, preferably at least 80%, more preferably at least 95%, or even at least 99%.
    [0021] The composition of the invention can be manufactured by dissolving its various compounds in a solvent (especially as described above). It is preferred to dissolve the terpolymer in the solvent before the second polymer. Optionally, the solvent can then be evaporated. Alternatively, the composition can be made in the melt, in the absence of a solvent. The invention notably provides films made from compositions according to the invention and deposited on a substrate. The substrate may, for example, be a polymeric substrate, such as a polyethylene terephthalate or polyethylene naphthalate substrate, or a substrate of paper, glass or silicon. Preferably, the film is deposited in solvent or molten route; then dried and annealed to crystallize (by heating at a temperature below the melting point of the composition, for a period greater than or equal to 1 minute).
    [0022] The invention also provides multilayer structures comprising at least one composition film of the invention and electrodes on either side. Such structures may in particular be made: by coating the composition on a substrate, evaporation of the solvent, annealing and deposition of electrodes by evaporation or sputtering of metal deposition, indium-tin oxide (ITO), deposition of a layer of conductive polymer, depositing a conductive layer from conducting inks based on silver, silver nanowires, or graphene ...; or by printing the composition on a substrate, for example by screen printing, gravure printing, offset printing, and then annealing and deposition of electrodes by evaporation or sputtering of metal deposition, indium tin oxide (ITO), depositing a conductive polymer layer, depositing a conductive layer from conductive inks based on silver, nano-silver son ... These multilayer structures can thus provide actuators. Other objects that can be made by the compositions of the invention include mutant-containing fibers, filaments, cables, and fibers, including a conductive core core made by solvent or extrusion. EXAMPLES The following examples illustrate the invention without limiting it. In order to characterize the electromechanical properties of the polymers, 15% by weight of electroactive polymer (s) are dissolved in methyl ethyl ketone in a heating flask surmounted by a refrigerated column. The mixture is carried out under reflux at 80 ° C., with magnetic stirring. After complete dissolution, the solution is filtered at 1 μm. The solution is then deposited under controlled atmosphere, by coating, on a glass plate. The solvent is allowed to evaporate for 12 hours. The films obtained are then brought to 80 ° C in an oven to remove traces of solvent. The films are then annealed at 115 ° C for 1 hour.
    [0023] Films are then placed at room temperature, the release of volatile compounds is examined visually and by touch after 12 hours. Films are covered with electrodes by vacuum evaporation of gold. Their dielectric properties are measured by impedance spectroscopy. Their mechanical properties are measured by dynamic mechanical analysis. In order to measure the electromechanical properties, the electrode films are fixed on flexible substrates of 100 μm polyethylene terephthalate by means of an adhesive (Scotch 3M ATG 924). The multilayers thus produced are then rolled for 15 minutes using a D & K 4468H laminator. The films are then fixed on supports. Each film face is connected to a pole of a variable voltage generator (Trek 609D-6). When the sample is subjected to a voltage, its deflection is measured using a laser deformation sensor (BAUMER CH8501). The longitudinal deformation of the polymer film 531 (E) is calculated from the mechanical properties of the different layers and the geometry of the samples. In Example 1, the polymer used is a P terpolymer (VDF-TrFECTFE) with a molar composition of 61.0 / 30.1 / 8.9. Example 2 is similar to Example 1, except that at the end of the dissolution of the polymer, 15% by weight is added relative to the non-crystalline polyester polymer of the polyester type (Palamoll 652 / BASF ).
    [0024] In Example 3, the procedure is as for Example 1, but at the end of the dissolution of the polymer is added 15% by weight relative to the non-polymeric plasticizer diethyl-hexyl phthalate polymer. This plasticizer is classified as carcinogenic, mutagenic and reprotoxic.
    [0025] S31 (10 V / pm) Release Eco-profile after 12 h toxicological Example 1 (comparative) 0.0025 None Good Example 2 0.2 None Good (Invention) Example 3 (Comparative) 0.4 High Bad It is found that the example corresponding to the invention makes it possible to obtain films and devices without salting out, with a good ecotoxicological profile and with improved low-field electromechanical properties.
    权利要求:
    Claims (17)
    [0001]
    REVENDICATIONS1. A composition comprising: - at least one electroactive fluorinated terpolymer, and - at least one second polymer compatible with the electroactive fluorinated terpolymer, and having a glass transition temperature lower than that of the electroactive fluorinated terpolymer.
    [0002]
    The composition of claim 1, wherein the second polymer has a glass transition temperature of at least 5 ° C, preferably at least 10 ° C, or at least 15 ° C, or at least 20 ° C, to that of the electroactive fluorinated terpolymer.
    [0003]
    A composition according to any one of claims 1 or 2, wherein the glass transition temperature of the electroactive fluorinated terpolymer is from -50 ° C to + 10 ° C, preferably from -40 ° C to 10 ° C; and / or the glass transition temperature of the second polymer is from -100 ° C to -0 ° C, preferably from -100 ° C to -40 ° C.
    [0004]
    4. A composition according to any one of claims 1 or 3, wherein the electroactive fluorinated terpolymer is a terpolymer of vinylidene fluoride, trifluoroethylene and a third monomer.
    [0005]
    The composition of claim 4, wherein the third monomer is chlorofluoro-1,1-ethylene or chlorotrifluoroethylene.
    [0006]
    6. Composition according to any one of claims 1 to 5, wherein the second polymer is a polyester, preferably selected from polyadipates, polyglutarates and polysébaçates.
    [0007]
    The composition of any one of claims 1 to 6, wherein the electroactive fluorinated terpolymer and the second polymer are present in a weight ratio of 50:50 to 99: 1, preferably 70:30 to 95: 5, more preferably from 80:20 to 90:10. 3031519 14
    [0008]
    8. Composition according to any one of claims 1 to 7, comprising at least one solvent, preferably chosen from tetrahydrofuran, methyl ethyl ketone, dimethylformamide, dimethylacetamide, tetramethylurea, dimethylsulfoxide, trimethylphosphate, N methyl-2-pyrrolidone, acetone, methyl isobutyl ketone, glycol ethers, glycol ether esters, N-butyl acetate, cyclohexanone, diacetone alcohol, diisobutyl ketone, ethyl acetoacetate, butyrolactone, isophorone, triethyl phosphate, carbitol acetate, propylene carbonate and glyceryl triacetate.
    [0009]
    The composition of any one of claims 1 to 8, wherein: the electroactive fluorinated terpolymer has a molecular weight of 200,000 to 1,500,000, preferably 250,000 to 1,000,000, more preferably 300,000. 700,000; and / or the second polymer has a molecular weight of from 500 to 700,000, preferably from 2,000 to 100,000, and more preferably from 5,000 to 20,000.
    [0010]
    10. Composition according to any one of claims 1 to 9, also comprising a fluorinated copolymer, in particular ferroelectric copolymer, preferably chosen from copolymers of vinylidene fluoride and trifluoroethylene, vinylidene fluoride and chlorotrifluoroethylene, vinylidene fluoride. and tetrafluoroethylene, and vinylidene fluoride and hexafluoropropylene.
    [0011]
    11. A method of manufacturing a composition according to any one of claims 1 to 10, comprising a step of mixing the electroactive fluorinated terpolymer with the second polymer.
    [0012]
    12. The manufacturing method according to claim 11, wherein the mixing is carried out in a solvent, preferably selected from tetrahydrofuran, methyl ethyl ketone, dimethylformamide, dimethylacetamide, tetramethylurea, dimethylsulfoxide, trimethylphosphate, N methyl-2-pyrrolidone, acetone, methyl isobutyl ketone, glycol ethers, glycol ether esters, N-butyl acetate, cyclohexanone, diacetone alcohol, diisobutyl ketone, ethyl acetoacetate butyrolactone, isophorone, triethylphosphate, carbitol acetate, propylene carbonate and glyceryl triacetate; preferably dissolving the electroactive fluorinated terpolymer and then the second polymer in the solvent.
    [0013]
    13. Device comprising a substrate, and a film of the composition according to one of claims 1 to 10 disposed thereon. 10
    [0014]
    14. Device according to claim 13, further comprising electrodes on either side of the film, said device preferably being an actuator.
    [0015]
    15. A method of manufacturing the device according to any one of claims 13 or 14, comprising a step of depositing the film on the substrate.
    [0016]
    16. The method of manufacturing the device of claim 15, wherein the step of depositing is a step of coating or printing the composition on the substrate.
    [0017]
    17. A method of manufacturing the device according to any one of claims 15 or 16, comprising a further electrode deposition step, preferably by evaporation or sputtering of metal, indium-tin oxide, a layer of conductive polymer, conductive ink based on silver, silver nanowires, or graphene. 30
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    同族专利:
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    FR2944285B1|2009-04-09|2011-11-25|Francois Bauer|PROCESS FOR PRODUCING TERPOLYMERS BASED ON VDF, TRFE AND CFE OR CTFE|
    JP6048870B2|2012-08-27|2016-12-21|独立行政法人国立高等専門学校機構|Method for manufacturing β-type polyvinylidene fluoride film, β-type polyvinylidene fluoride film, piezoelectric sensor provided with β-type polyvinylidene fluoride film, and method for manufacturing piezoelectric sensor|
    FR3004718B1|2013-04-18|2016-05-06|Inst Nat Sciences Appliquees Lyon|METHOD FOR MANUFACTURING POLARIZABLE COMPOSITE MATERIAL UNDER THE ACTION OF A LOW ELECTRIC FIELD|JP2021174834A|2020-04-22|2021-11-01|ダイキン工業株式会社|Fluorine-containing polymer film|
    法律状态:
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    2016-07-15| PLSC| Publication of the preliminary search report|Effective date: 20160715 |
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    优先权:
    申请号 | 申请日 | 专利标题
    FR1550291A|FR3031519B1|2015-01-14|2015-01-14|COMPOSITION BASED ON ELECTROACTIVE TERPOLYMER|FR1550291A| FR3031519B1|2015-01-14|2015-01-14|COMPOSITION BASED ON ELECTROACTIVE TERPOLYMER|
    EP16703569.0A| EP3245261A1|2015-01-14|2016-01-11|Composition based on electroactive terpolymer|
    PCT/FR2016/050042| WO2016113492A1|2015-01-14|2016-01-11|Composition based on electroactive terpolymer|
    CN201680005897.4A| CN107207893B|2015-01-14|2016-01-11|Composition based on electroactive terpolymer|
    JP2017537480A| JP6836993B2|2015-01-14|2016-01-11|Composition based on electroactive terpolymer|
    KR1020177022404A| KR20170106381A|2015-01-14|2016-01-11|Compositions based on electroactive terpolymers|
    US15/543,310| US10626285B2|2015-01-14|2016-01-11|Composition based on electroactive terpolymer|
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