WO2017169627A1 - 導電性膜およびその製造方法 - Google Patents
導電性膜およびその製造方法 Download PDFInfo
- Publication number
- WO2017169627A1 WO2017169627A1 PCT/JP2017/009470 JP2017009470W WO2017169627A1 WO 2017169627 A1 WO2017169627 A1 WO 2017169627A1 JP 2017009470 W JP2017009470 W JP 2017009470W WO 2017169627 A1 WO2017169627 A1 WO 2017169627A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- conductive film
- liquid composition
- conductive
- mass
- graphite powder
- Prior art date
Links
Images
Classifications
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B1/00—Conductors or conductive bodies characterised by the conductive materials; Selection of materials as conductors
- H01B1/20—Conductive material dispersed in non-conductive organic material
- H01B1/24—Conductive material dispersed in non-conductive organic material the conductive material comprising carbon-silicon compounds, carbon or silicon
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B13/00—Apparatus or processes specially adapted for manufacturing conductors or cables
- H01B13/0036—Details
-
- H—ELECTRICITY
- H01—ELECTRIC ELEMENTS
- H01B—CABLES; CONDUCTORS; INSULATORS; SELECTION OF MATERIALS FOR THEIR CONDUCTIVE, INSULATING OR DIELECTRIC PROPERTIES
- H01B5/00—Non-insulated conductors or conductive bodies characterised by their form
- H01B5/16—Non-insulated conductors or conductive bodies characterised by their form comprising conductive material in insulating or poorly conductive material, e.g. conductive rubber
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/09—Use of materials for the conductive, e.g. metallic pattern
- H05K1/092—Dispersed materials, e.g. conductive pastes or inks
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/0277—Bendability or stretchability details
- H05K1/0283—Stretchable printed circuits
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/03—Use of materials for the substrate
- H05K1/0393—Flexible materials
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/03—Conductive materials
- H05K2201/0302—Properties and characteristics in general
- H05K2201/0314—Elastomeric connector or conductor, e.g. rubber with metallic filler
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K2201/00—Indexing scheme relating to printed circuits covered by H05K1/00
- H05K2201/03—Conductive materials
- H05K2201/032—Materials
- H05K2201/0323—Carbon
Definitions
- the present invention relates to a conductive film suitable for a flexible transducer electrode and wiring, an electromagnetic wave shield, a flexible wiring board, and the like using a polymer material, and a manufacturing method thereof.
- the conductive agent when conductive carbon black or graphite powder is blended in the elastomer, the particles are difficult to contact with each other and the area of the contact point is small. For this reason, in order to give desired electroconductivity to a composition, the compounding quantity of a electrically conductive agent must be increased, and a softness
- Patent Document 2 describes a conductive film including an elastomer, a fibrous carbon material having a fiber diameter of less than 30 nm, and a flaky carbon material having a maximum length of 150 nm or more and a thickness of less than 50 nm. ing.
- the flaky carbon material connects the fibrous carbon materials to suppress an increase in electrical resistance during stretching.
- This invention is made in view of such a situation, and makes it a subject to provide the electroconductive film with high electroconductivity, and an electrical resistance which does not increase easily even if it repeats expansion
- the conductive film of the present invention includes an elastomer and a flaky carbon material, and the content of the flaky carbon material is 100 masses of the entire solid content excluding the conductive agent.
- the glossiness of the surface measured at an incident angle of 20 ° is larger than 0.4% and smaller than 10%.
- the glossiness of the surface measured at an incident angle of 20 ° is greater than 0.4%.
- the flaky carbon material is a material obtained by flaking graphite or the like.
- the electronic state of graphene, which is a structural unit of graphite, is close to that of metal. For this reason, the closer to thinning, the closer to graphene, and the metallic luster appears. Therefore, it is considered that as the glossiness of the surface is larger, more oriented flake carbon materials are present. Further, it is considered that there is a flaky carbon material that has been thinned (thinner).
- the aspect ratio (length / thickness) of the flaky carbon material is relatively large. For this reason, the flaky carbon materials are easily in contact with each other, and a conduction path is easily formed. In addition, since the flaky carbon material is oriented in the plane direction, the conduction path is not easily cut even if it extends. Therefore, in the conductive film of the present invention, the initial (before stretching) conductivity is high, and even if the stretching is repeated, the electrical resistance is hardly increased. That is, the conductive film of the present invention has excellent conductivity durability in the sense that high conductivity can be maintained.
- a first method for producing a conductive film of the present invention is a liquid composition comprising an elastomer, a conductive agent containing at least one of graphite powder and expanded graphite powder, and a solvent.
- a liquid composition preparation step for preparing the liquid composition a pulverization treatment step for pulverizing the liquid composition using a wet jet mill, and applying the liquid composition after the pulverization treatment to a substrate to cure the coating film
- a curing step for obtaining a conductive film having a surface glossiness of greater than 0.4% and less than 10% measured at an incident angle of 20 °.
- the liquid composition is pulverized by a wet jet mill, whereby the graphite (expanded graphite) in the liquid composition is peeled off by shearing force, and flaking progresses.
- the multilayer graphene in which the number of graphene layers is smaller than that of the raw material graphite (expanded graphite) is produced.
- the multilayer graphene is included in the exfoliated carbon material in the conductive film of the present invention.
- the said liquid composition is apply
- the flaky carbon material can be easily manufactured, and the conductive film of the present invention can be easily manufactured.
- pulverization process can be implemented by higher solid content concentration compared with the 2nd manufacturing method of this invention demonstrated below, the adjustment range of solid content concentration and a viscosity of a liquid composition becomes wide.
- the raw material carbon material is processed by a bead mill. For this reason, fine particle formation by breakage is more likely to proceed than thinning by peeling of the carbon material. Therefore, multilayer graphene (flaky carbon material) for realizing a conductive film having a predetermined glossiness cannot be obtained.
- a second method for producing a conductive film of the present invention includes a conductive agent dispersion containing a conductive agent containing at least one of graphite powder and expanded graphite powder, and a solvent.
- a pulverizing treatment step using a wet jet mill a liquid composition preparing step for preparing a liquid composition by adding an elastomer solution containing an elastomer and a solvent to the conductive agent dispersion after the pulverizing treatment,
- the conductive agent dispersion is pulverized by a wet jet mill, whereby the graphite (expanded graphite) in the conductive agent dispersion is peeled off by shearing force, and thinning proceeds.
- multi-layer graphene having a smaller number of graphene layers than raw material graphite (expanded graphite) is produced, as in the pulverization step in the first production method. That is, in the pulverization treatment step in the second production method of the present invention, a conductive agent dispersion liquid in which multilayer graphene (flaky carbon material) or the like is dispersed in a solvent is obtained.
- the liquid composition preparation step the liquid composition is prepared by adding an elastomer solution to the conductive agent dispersion. And like the hardening process in a 1st manufacturing method, the said liquid composition is apply
- the flaky carbon material can be easily manufactured, and the conductive film of the present invention can be easily manufactured.
- the molecular weight of the polymer is reduced by the pulverization treatment as compared with the first production method of the present invention.
- the conductive film of the present invention includes an elastomer and a flaky carbon material.
- the elastomer it is desirable to use one having a glass transition temperature (Tg) of room temperature or less from the viewpoint of having rubber-like elasticity at room temperature.
- Tg glass transition temperature
- crystallinity is lowered.
- the elastomer is more easily expanded and contracted.
- Tg glass transition temperature
- those having a Tg of 0 ° C. or lower, ⁇ 10 ° C. or lower, and further ⁇ 30 ° C. or lower are more flexible and suitable.
- the elastomer is desirably a crosslinked rubber because it has excellent resilience when it is repeatedly deformed. Moreover, it may have a microphase separation structure of a hard segment and a soft segment, and may be pseudo-crosslinked like a thermoplastic elastomer. Examples of the thermoplastic elastomer include olefin, styrene, polyester, acrylic, urethane, and vinyl chloride.
- Crosslinked rubbers include urethane rubber, acrylic rubber, silicone rubber, butyl rubber, butadiene rubber, ethylene oxide-epichlorohydrin copolymer, nitrile rubber, hydrogenated nitrile rubber, chloroprene rubber, natural rubber, isoprene rubber, styrene-butadiene rubber. Ethylene-propylene-diene copolymer (EPDM), polyester rubber, fluororubber and the like. Further, it may be modified by introducing a functional group, such as epoxidized natural rubber or carboxyl group-modified hydrogenated nitrile rubber.
- acrylic rubber has low crystallinity and weak intermolecular force, and therefore has a lower Tg than other rubbers. Therefore, it is flexible and stretchable, and is suitable for an electrode of a transducer.
- acrylic rubber for example, one having an elongation in an uncrosslinked state of 1500% or more and a tensile strength of 0.1 MPa or more is desirable.
- elongation and tensile strength in the uncrosslinked state values obtained from the stress-elongation curve measured by the following method are adopted. First, the acrylic rubber polymer solution before crosslinking is applied on a release-treated polyethylene terephthalate (PET) base material at a thickness target value of 500 ⁇ m and dried at 150 ° C. for 2 hours.
- PET polyethylene terephthalate
- the base material on which the coating film is formed is cut into a size of width 10 mm ⁇ length 40 mm, and the coating film is peeled therefrom to form a test piece. Then, a tensile test of the test piece was performed using a static test machine “AUTOGRAPH AGS-X (100N)” manufactured by Shimadzu Corporation. Measure the elongation to stress.
- an elastomer having a low Tg may be selected.
- those having a Tg of ⁇ 30 ° C. or less are suitable.
- an elastomer having a low Tg may be used alone, or may be used by blending with another elastomer.
- cold resistance can be improved.
- the cold resistance of the conductive film is increased, the flexibility is not easily lowered even at a low temperature, and an increase in electrical resistance can be suppressed even if the stretching is repeated.
- the flaky carbon material can be produced from a carbon material having a graphite structure such as graphite or expanded graphite.
- the flaky carbon material is preferably a multilayer graphene that is a stack of a plurality of graphenes.
- Graphene is a layer of graphite (graphite) and has a structure in which six-membered rings of carbon atoms are connected in a planar shape.
- the number of stacked graphene layers in the multilayer graphene is less than that of graphite, and is preferably several to several hundreds.
- the content of the flaky carbon material in the conductive film of the present invention is 20 parts by mass or more and 60 parts by mass or less when the total solid content excluding the conductive agent is 100 parts by mass.
- the amount is less than 20 parts by mass, the flaky carbon materials are difficult to contact with each other, and a conduction path that can withstand extension cannot be formed.
- the glossiness of the surface of the conductive film is considered to be 0.4% or less.
- flexibility of an electroconductive film will fall.
- the conductive agent is a material that imparts conductivity to the conductive film including the flaky carbon material.
- the glossiness of the surface of the conductive film of the present invention is larger than 0.4% and smaller than 10% when measured at an incident angle of 20 °. In the case of 0.4% or less, since the exfoliated carbon material is not sufficiently oriented, desired conductivity cannot be obtained. A suitable glossiness is 0.5% or more. On the other hand, if it is 10% or more, the flexibility of the conductive film is lowered, and the durability when repeatedly stretched is lowered. The preferred glossiness is 5% or less. More preferably, it is 1.5% or less.
- the conductive film of the present invention may contain other conductive agent in addition to the flaky carbon material.
- conductive carbon black conductive carbon black, carbon nanotubes and the like are suitable.
- the viscosity of a liquid composition can be adjusted as a thickener, or the intensity
- the conductive film of the present invention may contain additives such as a crosslinking agent, a crosslinking accelerator, a crosslinking aid, a dispersant, a plasticizer, a processing aid, an antiaging agent, a softening agent, and a coloring agent. What is necessary is just to select suitably about the crosslinking agent, crosslinking accelerator, crosslinking adjuvant, etc. which contribute to a crosslinking reaction according to the kind of elastomer. When a plasticizer is included, the cold resistance of the conductive film is improved. Examples of the plasticizer include adipic acid diesters and ether / ester derivatives.
- a dispersant When a dispersant is included, aggregation of the flaky carbon material is suppressed and dispersibility is improved.
- the dispersant include a polymer surfactant having an organic salt structure in which an anion and a cation are ionically bonded (for example, a high molecular weight polyester acid amidoamine salt), an amide bond or an imide bond between a polycyclic aromatic component and an oligomer component. And the like.
- the polycyclic aromatic component of the latter polymer has a ⁇ - ⁇ interaction and contributes to the affinity with the flaky carbon material.
- the polycyclic aromatic component has a plurality of ring structures including an aromatic ring. The number and arrangement of the rings are not particularly limited.
- the polycyclic aromatic component desirably has, for example, any of a benzene ring, a naphthalene ring, an anthracene ring, a phenanthrene ring, a pyrene ring, a perylene ring, and a naphthacene ring.
- a biphenyl structure in which a benzene ring is connected and a structure having a naphthalene ring are preferable.
- the oligomer component having an amide bond or an imide bond with the polycyclic aromatic component contributes to the affinity with the elastomer.
- the oligomer component is preferably compatible with the elastomer.
- the first production method of the conductive film of the present invention includes a liquid composition preparation step, a pulverization treatment step, and a curing step. Hereinafter, each process is demonstrated in order.
- This step is a step of preparing a liquid composition containing an elastomer, a conductive agent containing at least one of graphite powder and expanded graphite powder, and a solvent.
- the elastomer is as described in the conductive film of the present invention.
- a rubber polymer or a thermoplastic elastomer before crosslinking may be used.
- graphite powder for the conductive agent natural graphite or artificial graphite powder may be used.
- Exfoliated graphite powder that has been exfoliated may be used.
- Expanded graphite is obtained by inserting a substance that generates gas by heating between layers of scaly graphite.
- the expanded graphite powder may be natural graphite or artificial graphite.
- expanded graphite powder exfoliated expanded graphite powder that has been exfoliated may be used.
- the particle diameters of graphite powder and expanded graphite powder are desirably relatively large as long as they can be processed by a wet jet mill.
- the particle diameter of the raw material powder is small, the length (area) in the surface direction of the multilayer graphene (flaky carbon material) obtained after the pulverization process is also small.
- the multilayer graphenes are difficult to contact each other.
- the average particle diameter of the graphite powder and the expanded graphite powder is desirably 45 ⁇ m or more.
- the median diameter measured by a laser diffraction scattering type particle size distribution measuring device (“Microtrack MT3000” manufactured by Microtrack Bell Co., Ltd.) is used as the average particle size of graphite powder and expanded graphite powder. To do.
- a dispersion liquid (refractive index: 1.38) in which powder to be measured is dispersed in methyl ethyl ketone is used.
- the blending amounts of the graphite powder and the expanded graphite powder are 20 parts by mass or more and 60 parts by mass or less when the total solid content excluding the conductive agent is 100 parts by mass.
- the amount is less than 20 parts by mass, it is difficult to produce a conductive film having a surface glossiness of greater than 0.4%.
- the multilayer graphenes are not easily in contact with each other, and a conduction path that can withstand extension cannot be formed.
- it exceeds 60 parts by mass it becomes difficult to produce a flexible conductive film.
- the liquid composition may contain a conductive agent other than graphite powder and expanded graphite powder.
- a conductive agent other than graphite powder and expanded graphite powder.
- conductive carbon black, carbon nanotubes and the like are suitable.
- the solvent is preferably a solvent that can dissolve the elastomeric polymer.
- a solvent that can dissolve the elastomeric polymer For example, butyl cellosolve acetate, acetylacetone, isophorone or the like may be used. Moreover, it is good to adjust the boiling point of a solvent according to the application
- Liquid compositions include additives such as crosslinking agents, crosslinking accelerators, crosslinking aids, dispersants, plasticizers, processing aids, anti-aging agents, softeners, colorants, antifoaming agents, leveling agents, viscosity modifiers, etc. May be included. What is necessary is just to select suitably about the crosslinking agent, crosslinking accelerator, crosslinking adjuvant, etc. which contribute to a crosslinking reaction according to the kind of elastomer.
- the plasticizer and the dispersant are as described in the conductive film of the present invention.
- the total solid content excluding the conductive agent and the plasticizer is preferably 5 parts by mass or more and 35 parts by mass or less based on 100 parts by mass.
- a dispersant it is preferable that the total solid content excluding the conductive agent is 5 parts by mass or more and 40 parts by mass or less based on 100 parts by mass.
- This step is a step of pulverizing the liquid composition prepared in the previous step using a wet jet mill.
- the liquid composition is pressurized by a high-pressure pump and fed into a nozzle, and is jetted at a high speed from the nozzle. Then, the graphite powder and the like in the liquid composition are pulverized by high-speed shearing force generated when passing through the nozzle, cavitation, and impact force caused by collision with a wall or collision between liquid compositions. According to the wet jet mill, peeling is likely to proceed because a shearing force is applied to the graphite powder and the expanded graphite powder. Thereby, the multilayer graphene (flaky carbon material) of nanometer order can be obtained easily.
- a nozzle having a shape that easily causes collision with a wall or collision between liquid compositions such as a collision (cross) type nozzle, may be selected.
- the method for applying the liquid composition is not particularly limited.
- printing methods such as ink jet printing, flexographic printing, gravure printing, screen printing, pad printing, metal mask printing, and lithography
- a sheet having stretchability or flexibility is suitable.
- acrylic rubber EPDM, nitrile rubber, hydrogenated nitrile rubber, urethane rubber, butyl rubber, silicone rubber, chloroprene rubber, cross-linked rubber such as ethylene-vinyl acetate copolymer, or urethane, ester, amide, acrylic
- an elastomer sheet made of a thermoplastic elastomer such as polyimide, polyethylene, PET, polyethylene naphthalate (PEN) and the like.
- the curing temperature of the coating film may be appropriately determined in consideration of the type of solvent used and the crosslinking temperature of the elastomer. What is necessary is just to determine the thickness of a conductive film suitably according to a use. For example, when used as an electrode or wiring of a transducer, the thickness is preferably 1 ⁇ m or more and 500 ⁇ m or less.
- the second manufacturing method of the conductive film of the present invention includes a pulverization treatment step, a liquid composition preparation step, and a curing step. Hereinafter, each process is demonstrated in order.
- This step is a step of pulverizing a conductive agent dispersion containing a conductive agent containing at least one of graphite powder and expanded graphite powder and a solvent using a wet jet mill.
- This step is the same as the liquid composition preparation step of the first method for producing a conductive film of the present invention described above, except that the conductive agent dispersion is not pulverized but a liquid composition. That is, the conductive agent dispersion may be sprayed from the nozzle of the wet jet mill instead of the liquid composition.
- the conductive agent and the solvent contained in the conductive agent dispersion are as described in the first production method.
- the solvent is preferably the same as the solvent used to prepare the elastomer solution in the next step. When using a dispersing agent, it is desirable to mix
- Liquid composition preparation step This step is a step of preparing a liquid composition by adding an elastomer solution containing an elastomer and a solvent to the conductive agent dispersion after pulverization.
- the elastomer and the solvent are as described in the first production method.
- the liquid composition comprises a crosslinking agent, a crosslinking accelerator, a crosslinking aid, a plasticizer, a processing aid, an anti-aging agent, a softening agent, a colorant, an antifoaming agent, and a leveling agent.
- additives such as viscosity modifiers may be included.
- the liquid composition prepared in the previous step is applied to a substrate and the coating film is cured, so that the glossiness of the surface measured at an incident angle of 20 ° is greater than 0.4% and 10 % Is a step of obtaining a conductive film smaller than%.
- This step is the same as the curing step of the first method for producing the conductive film of the present invention described above.
- Conductive films were produced using the raw materials shown in Table 1 at the blending ratios shown in Tables 2 to 4.
- glycidyl ether group-modified acrylic rubber polymer-1 was produced by suspension polymerization of three types of monomers. As monomers, ethyl acrylate (EA), acrylonitrile (AN), and allyl glycidyl ether (AGE) were used. The blending ratio of the monomers was 96 mass% EA, 2 mass% AN, and 2 mass% AGE. The resulting acrylic rubber polymer had a Tg of ⁇ 10 ° C.
- the conductive agent (F) was produced by wet pulverizing multi-walled carbon nanotubes (“VGCF (registered trademark)” manufactured by Showa Denko KK, fiber diameter 150 nm, length 10 ⁇ m).
- VGCF registered trademark
- the wet pulverization was performed by putting the multi-walled carbon nanotubes in a bead mill together with methyl ethyl ketone and a peripheral speed of 10 m / s and a residence time of 15 minutes.
- zirconia beads having a diameter of 0.5 mm were used (hereinafter the same).
- the dispersant (b) is naphthalene-1,4,5,8-tetracarboxylic dianhydride (NTCDA) -polyetherimide.
- NTCDA naphthalene-1,4,5,8-tetracarboxylic dianhydride
- NTCDA solvent tetrahydrofuran
- THF solvent tetrahydrofuran
- 30.00 g (15.00 mmol) of poly (propylene glycol) bis (2-aminopropyl ether) (“Jeffamine (registered trademark) D2000” manufactured by Huntsman Corporation, molecular weight 2000) of both-end amino-modified polyether was weighed. Then, the mixture was poured into a three-necked flask while stirring, and the polymerization reaction was performed by heating and refluxing at 65 ° C.
- NTCDA-polyetheramide having a structure represented by the formula (b-1).
- NTCDA-polyetheramide was placed in an eggplant flask, heated and refluxed at 200 ° C. for 6 hours, and then dried under reduced pressure to obtain NTCDA-polyetherimide having the structure represented by formula (b-2).
- the dispersant (e) is a polymer represented by the following structural formula (e).
- the weight average molecular weight of the polymer of structural formula (e) is about 1500.
- a liquid composition was prepared by adding a conductive agent, a dispersant, a crosslinking agent, and a crosslinking accelerator to a polymer solution in which the polymer was dissolved in butyl cellosolve acetate.
- the liquid composition was pulverized by a wet jet mill (“Nanovaita (registered trademark)” manufactured by Yoshida Kikai Kogyo Co., Ltd.). By the pass operation, the pulverization process was performed a total of 6 times (6-pass process).
- the first pass was performed with a straight nozzle (nozzle diameter 170 ⁇ m) and a processing pressure of 90 MPa
- the second and subsequent passes were performed with a cross-type nozzle (nozzle diameter 170 ⁇ m) and a processing pressure of 130 MPa.
- the liquid composition after the pulverization treatment was applied onto a substrate at a target thickness of 20 ⁇ m by a bar coating method, and heated at 150 ° C. for 2 hours to cure the coating film.
- a base material two types, a PET sheet and a thermoplastic elastomer sheet (“Esmer (registered trademark) URS” manufactured by Nippon Matai Co., Ltd., thickness 0.2 mm), were used.
- the conductive films of Examples 12 and 13 were produced by the second production method of the present invention.
- a dispersant and a solvent were added to the conductive agent to prepare a conductive agent dispersion.
- the prepared conductive agent dispersion was pulverized by a wet jet mill (same as above).
- the pass operation the pulverization process was performed three times in total (3-pass process).
- the first pass was performed with a straight nozzle (nozzle diameter 170 ⁇ m) and a processing pressure of 90 MPa
- the second and subsequent passes were performed with a cross-type nozzle (nozzle diameter 170 ⁇ m) and a processing pressure of 130 MPa.
- a polymer solution prepared by dissolving the polymer in a solvent, a crosslinking agent, and a crosslinking accelerator were added to and mixed with the conductive agent dispersion after the pulverization treatment to prepare a liquid composition.
- the obtained liquid composition was applied onto a substrate at a target thickness of 20 ⁇ m by a bar coating method and heated at 150 ° C. for 2 hours to cure the coating film.
- a base material two types, a PET sheet and a thermoplastic elastomer sheet (same as above), were used.
- the polymer solution in an Example is contained in the concept of the elastomer solution in this invention.
- a conductive composition, a dispersing agent, a crosslinking agent, and a crosslinking accelerator were added to a polymer solution in which the polymer was dissolved in butyl cellosolve acetate to prepare a liquid composition.
- the prepared liquid composition was put into a bead mill and treated at a peripheral speed of 10 m / s and a residence time of 15 minutes.
- the treated liquid composition was cured in the same manner as in Example 1.
- glycidyl ether group-modified acrylic rubber polymer-2 was produced by suspension polymerization of three types of monomers. As monomers, butyl acrylate (BA), acrylonitrile (AN), and allyl glycidyl ether (AGE) were used. The blending ratio of the monomers was 96% by mass of BA, 2% by mass of AN, and 2% by mass of AGE. The resulting acrylic rubber polymer had a Tg of ⁇ 45 ° C.
- the ternary fluororubber polymer is a vinylidene fluoride-tetrafluoroethylene-hexafluoropropylene copolymer.
- Examples 15 to 25 The conductive films of Examples 15 to 25 were manufactured by the first manufacturing method of the present invention.
- a liquid composition was prepared by adding a conductive agent, a dispersing agent, a crosslinking agent, and a crosslinking accelerator to a polymer solution in which the polymer was dissolved in butyl cellosolve acetate.
- a plasticizer was also added.
- a polymer solution was prepared by first dissolving a processing aid added to a polymer by kneading in isophorone containing 1.6% by mass of acetic acid.
- the liquid composition was pulverized by a wet jet mill (same as above).
- the pulverization process was performed a total of 6 times (6-pass process).
- the first pass was performed with a straight nozzle (nozzle diameter 170 ⁇ m) and a processing pressure of 90 MPa
- the second and subsequent passes were performed with a cross-type nozzle (nozzle diameter 170 ⁇ m) and a processing pressure of 130 MPa.
- the liquid composition after the pulverization treatment was applied onto a substrate at a target thickness of 20 ⁇ m by a bar coating method, and heated at 150 ° C. for 2 hours to cure the coating film.
- a base material two types, a PET sheet and a thermoplastic elastomer sheet (same as above), were used.
- the volume resistivity of a 20 ⁇ m thick conductive film formed on a PET sheet was measured using a low resistivity meter “Loresta (registered trademark) GP” manufactured by Mitsubishi Chemical Analytech Co., Ltd. (voltage: 5 V, JIS K7194: 1994). ). The measured volume resistivity was taken as the initial electrical resistivity (before stretching).
- Tables 2 to 4 above summarize the evaluation results of the conductive films of Examples 1 to 14 and Comparative Examples 1 to 5.
- Tables 6 and 7 collectively show the evaluation results of the conductive films of Examples 15 to 25.
- FIG. 1 is a graph showing the relationship between the glossiness of the conductive film and the initial electrical resistivity.
- FIG. 2 is a graph showing the relationship between the glossiness of the conductive film and the maximum electrical resistivity in the extension durability test.
- the glossiness of the conductive films of Examples 1 to 14 was 0.5% or more and was larger than 0.4%.
- the initial electrical resistivity was as small as 0.050 ⁇ ⁇ cm or less, and the maximum electrical resistivity during the extension durability test was as small as 0.95 ⁇ ⁇ cm or less.
- the glossiness of the conductive films of Examples 15 to 25 was 0.5% or more and greater than 0.4%.
- the initial electrical resistivity was as small as 0.031 ⁇ ⁇ cm or less, and the maximum electrical resistivity during the extension durability test was as small as 1.46 ⁇ ⁇ cm or less.
- the glossiness of the conductive films of Comparative Examples 1 to 5 was 0.4% or less.
- the initial electrical resistivity of the conductive films of Comparative Examples 1 to 5 was larger than that of the conductive films of Examples 1 to 25.
- the maximum electrical resistivity during the extension durability test of the conductive films of Comparative Examples 1 to 4 was significantly higher than that of the conductive films of Examples 1 to 25.
- the group of comparative examples (Comparative Examples 1 to 5) and the group of Examples (Examples 1 to 25) can be divided with a glossiness of 0.4% as a boundary. It corresponds to the magnitude of the initial electrical resistivity. That is, the initial electrical resistivity is large in the group of comparative examples, and the initial electrical resistivity is small in the group of examples.
- the group of the comparative example and the group of the example divided with the glossiness of 0.4% as a boundary coincide with the magnitude of the maximum electrical resistivity.
- Comparative Example 3 the same conductive agent (B) as in Example 9, that is, expanded graphite powder was used. However, in Comparative Example 3, since the liquid composition was processed by the bead mill, the fine particles by breakage proceed more easily than the thinning by exfoliation of the expanded graphite. For this reason, it is considered that the conductive agents are less likely to contact each other, and the initial electrical resistivity and the maximum electrical resistivity during the extension durability test are increased. This can be confirmed from the fact that the glossiness of the conductive film of Comparative Example 3 is 0.4%.
- Comparative Example 5 two types of conductive agents (E) and (F) were used.
- the conductive agent (E) is a multi-walled carbon nanotube
- the conductive agent (F) is a pulverized product of the multi-walled carbon nanotube.
- a bead mill was used to pulverize the multi-walled carbon nanotubes, and the liquid composition was also treated with the bead mill. For this reason, it is considered that flaking by pulverization does not easily proceed, and the flaked carbon material could not be generated sufficiently. This can also be confirmed from the fact that the glossiness of the conductive film of Comparative Example 5 is 0.3%.
- the conductive film of the present invention has high initial conductivity, and it is difficult for the electrical resistance to increase even if the stretching is repeated. Moreover, according to the manufacturing method of the electroconductive film of this invention, it was confirmed that the said electroconductive film can be manufactured easily.
- the conductive film and the manufacturing method thereof of the present invention are suitable for an electromagnetic wave shield, a flexible wiring board, and the like used for a wearable device in addition to electrodes and wiring used for a flexible transducer.
- an electrode or wiring By using the conductive film of the present invention for an electrode or wiring, durability of an electronic device mounted on a flexible part such as a movable part of a robot, a care device, or an interior of a transportation device can be improved.
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Physics & Mathematics (AREA)
- Spectroscopy & Molecular Physics (AREA)
- Manufacturing & Machinery (AREA)
- Microelectronics & Electronic Packaging (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Conductive Materials (AREA)
- Manufacturing Of Electric Cables (AREA)
Abstract
Description
本発明の導電性膜は、エラストマーと、薄片状炭素材料と、を含む。エラストマーとしては、常温でゴム状弾性を有するという観点から、ガラス転移温度(Tg)が室温以下のものを用いることが望ましい。Tgが低くなると、結晶性が低下する。このため、エラストマーが、より伸縮しやすくなる。例えば、Tgが0℃以下、-10℃以下、さらには-30℃以下のものが、より柔軟で好適である。
(1)第一の製造方法
本発明の導電性膜の第一の製造方法は、液状組成物調製工程と、粉砕処理工程と、硬化工程と、を有する。以下、各工程を順に説明する。
本工程は、エラストマーと、黒鉛粉末および膨張黒鉛粉末の少なくとも一方を含む導電剤と、溶剤と、を含む液状組成物を調製する工程である。
本工程は、先の工程にて調製された液状組成物を湿式ジェットミルを用いて粉砕処理する工程である。
本工程は、粉砕処理後の液状組成物を基材に塗布し、塗膜を硬化させることにより、入射角20°で測定される表面の光沢度が0.4%より大きく10%より小さい導電性膜を得る工程である。
本発明の導電性膜の第二の製造方法は、粉砕処理工程と、液状組成物調製工程と、硬化工程と、を有する。以下、各工程を順に説明する。
本工程は、黒鉛粉末および膨張黒鉛粉末の少なくとも一方を含む導電剤と、溶剤と、を含む導電剤分散液を、湿式ジェットミルを用いて粉砕処理する工程である。本工程は、液状組成物ではなく導電剤分散液を粉砕処理する以外は、上述した本発明の導電性膜の第一の製造方法の液状組成物調製工程と、同じである。すなわち、液状組成物の代わりに導電剤分散液を、湿式ジェットミルのノズルから噴射させればよい。また、導電剤分散液に含まれる導電剤、溶剤については、第一の製造方法において説明した通りである。溶剤は、次の工程でエラストマー溶液を調製するために使用する溶剤と同じであることが望ましい。分散剤を使用する場合には、本工程の導電剤分散液に配合しておくことが望ましい。
本工程は、粉砕処理後の導電剤分散液に、エラストマーと溶剤とを含むエラストマー溶液を加えて液状組成物を調製する工程である。エラストマー、溶剤については、第一の製造方法において説明した通りである。また、第一の製造方法と同様に、液状組成物は、架橋剤、架橋促進剤、架橋助剤、可塑剤、加工助剤、老化防止剤、軟化剤、着色剤、消泡剤、レベリング剤、粘度調整剤などの添加剤を含んでいてもよい。
本工程は、先の工程にて調製された液状組成物を基材に塗布し、塗膜を硬化させることにより、入射角20°で測定される表面の光沢度が0.4%より大きく10%より小さい導電性膜を得る工程である。本工程は、上述した本発明の導電性膜の第一の製造方法の硬化工程と、同じである。
(1)表1に示す原料を、表2~表4に示す配合割合で使用して、導電性膜を製造した。表1中、グリシジルエーテル基変性アクリルゴムポリマー-1は、三種類のモノマーを懸濁重合して製造した。モノマーとしては、エチルアクリレート(EA)、アクリロニトリル(AN)、およびアリルグリシジルエーテル(AGE)を用いた。モノマーの配合割合は、EAを96質量%、ANを2質量%、AGEを2質量%とした。得られたアクリルゴムポリマーのTgは、-10℃であった。
実施例1~11、14、比較例1、4の導電性膜については、本発明の第一の製造方法で製造した。まず、ポリマーをブチルセロソロブアセテートに溶解したポリマー溶液に、導電剤、分散剤、架橋剤、および架橋促進剤を添加して液状組成物を調製した。次に、液状組成物を、湿式ジェットミル(吉田機械興業(株)製「ナノヴェイタ(登録商標)」)により粉砕処理した。パス運転により、粉砕処理を合計6回行った(6パス処理)。1パス目は、ストレート型ノズル(ノズル径170μm)、処理圧力90MPaで行い、2パス目以降は、クロス型ノズル(ノズル径170μm)、処理圧力130MPaで行った。粉砕処理後の液状組成物をバーコート法により基材上に厚さ狙い値20μmにて塗布し、150℃下で2時間加熱することにより、塗膜を硬化させた。基材としては、PETシート、熱可塑性エラストマーシート(日本マタイ(株)製「エスマー(登録商標)URS」、厚さ0.2mm)の二種類を使用した。
実施例12、13の導電性膜は、本発明の第二の製造方法で製造した。まず、導電剤に分散剤および溶剤を添加して導電剤分散液を調製した。次に、調製した導電剤分散液を、湿式ジェットミル(同上)により粉砕処理した。パス運転により、粉砕処理を合計3回行った(3パス処理)。1パス目は、ストレート型ノズル(ノズル径170μm)、処理圧力90MPaで行い、2パス目以降は、クロス型ノズル(ノズル径170μm)、処理圧力130MPaで行った。それから、粉砕処理後の導電剤分散液に、ポリマーを溶剤に溶解したポリマー溶液、架橋剤、架橋促進剤を添加、混合して液状組成物を調製した。得られた液状組成物をバーコート法により基材上に厚さ狙い値20μmにて塗布し、150℃下で2時間加熱することにより、塗膜を硬化させた。基材としては、PETシート、熱可塑性エラストマーシート(同上)の二種類を使用した。なお、実施例におけるポリマー溶液は、本発明におけるエラストマー溶液の概念に含まれる。
ポリマーに導電剤、分散剤、架橋剤、架橋促進剤、およびブチルセロソロブアセテートを添加して、三本ロールにより混練りして液状組成物を調製した。得られた液状組成物を、実施例1と同様にして硬化させた。
ポリマーをブチルセロソロブアセテートに溶解したポリマー溶液に、導電剤、分散剤、架橋剤、および架橋促進剤を添加して、液状組成物を調製した。調製した液状組成物をビーズミルに入れ、周速10m/s、滞留時間15分間にて処理した。処理後の液状組成物を、実施例1と同様にして硬化させた。
ポリマーをブチルセロソロブアセテートに溶解したポリマー溶液に、分散剤を添加した後、さらに導電剤を添加して、液状組成物を調製した。調製した液状組成物をビーズミルに入れ、周速10m/s、滞留時間15分間にて処理した。処理後の液状組成物を、実施例1と同様にして硬化させた。
実施例15~25の導電性膜については、本発明の第一の製造方法で製造した。実施例15~24においては、まず、ポリマーをブチルセロソロブアセテートに溶解したポリマー溶液に、導電剤、分散剤、架橋剤、および架橋促進剤を添加して液状組成物を調製した。ここで、実施例22~24については、可塑剤も添加した。実施例25においては、まず、ポリマーに加工助剤を練り加工により添加したものを、1.6質量%の酢酸を含有したイソホロンに溶解して、ポリマー溶液を調製した。そして、調製したポリマー溶液に、導電剤、分散剤、および架橋剤を添加して液状組成物を調製した。次に、液状組成物を、湿式ジェットミル(同上)により粉砕処理した。パス運転により、粉砕処理を合計6回行った(6パス処理)。1パス目は、ストレート型ノズル(ノズル径170μm)、処理圧力90MPaで行い、2パス目以降は、クロス型ノズル(ノズル径170μm)、処理圧力130MPaで行った。粉砕処理後の液状組成物をバーコート法により基材上に厚さ狙い値20μmにて塗布し、150℃下で2時間加熱することにより、塗膜を硬化させた。基材としては、PETシート、熱可塑性エラストマーシート(同上)の二種類を使用した。
[光沢度]
PETシート上に形成された厚さ20μmの導電性膜の表面を、日本電色工業(株)製の光沢計「PG-1M」を用いて、入射角20°にて測定した。
PETシート上に形成された厚さ20μmの導電性膜の体積抵抗率を、(株)三菱化学アナリテック製の低抵抗率計「ロレスタ(登録商標)GP」(電圧:5V、JIS K7194:1994に準拠)を用いて測定した。測定された体積抵抗率を、初期(伸張前)の電気抵抗率とした。
熱可塑性エラストマーシート上に厚さ20μmの導電性膜が形成されたサンプルを、JIS K6251:2010に規定されるダンベル状2号形に切り出して、試験片を作製した。試験片の両端から10mmの位置に銅箔を取り付けた。試験片の長手方向中心から両側10mmの位置に一対の標線を引き、試験片上に20mmの標線間距離を設定した。まず、1Vの電圧を印加した時の銅箔間の電気抵抗値R1を測定した。次に、試験片の一端を引っ張り、標線間距離が30mmになるまで伸張させた後(伸張率50%)、元の状態に戻した。この伸縮を、1Vの電圧を印加しながら周波数3.4Hzにて25000回繰り返し、銅箔間の電気抵抗値を測定した。測定された電気抵抗値の最大値R2を、電気抵抗値R1で除して、変化倍率(R2/R1)を算出した。そして、算出された変化倍率を、上述した初期の電気抵抗率に乗じて、伸張耐久試験における最大電気抵抗率とした。
先の表2~表4に、実施例1~14および比較例1~5の導電性膜の評価結果をまとめて示す。先の表6、表7に、実施例15~25の導電性膜の評価結果をまとめて示す。図1に、導電性膜の光沢度と初期の電気抵抗率との関係をグラフで示す。図2に、導電性膜の光沢度と伸張耐久試験における最大電気抵抗率との関係をグラフで示す。
Claims (11)
- エラストマーと、薄片状炭素材料と、を含み、
該薄片状炭素材料の含有量は、導電剤を除く固形分全体を100質量部とした場合の20質量部以上60質量部以下であり、
入射角20°で測定される表面の光沢度が0.4%より大きく10%より小さいことを特徴とする導電性膜。 - 前記薄片状炭素材料は、複層グラフェンである請求項1に記載の導電性膜。
- さらに、導電性カーボンブラックを含む請求項1または請求項2に記載の導電性膜。
- さらに、分散剤を含む請求項1ないし請求項3のいずれかに記載の導電性膜。
- エラストマーと、黒鉛粉末および膨張黒鉛粉末の少なくとも一方を含む導電剤と、溶剤と、を含む液状組成物を調製する液状組成物調製工程と、
該液状組成物を湿式ジェットミルを用いて粉砕処理する粉砕処理工程と、
粉砕処理後の該液状組成物を基材に塗布し、塗膜を硬化させることにより、入射角20°で測定される表面の光沢度が0.4%より大きく10%より小さい導電性膜を得る硬化工程と、
を有することを特徴とする導電性膜の製造方法。 - 前記液状組成物は、分散剤を含む請求項5に記載の導電性膜の製造方法。
- 黒鉛粉末および膨張黒鉛粉末の少なくとも一方を含む導電剤と、溶剤と、を含む導電剤分散液を、湿式ジェットミルを用いて粉砕処理する粉砕処理工程と、
粉砕処理後の該導電剤分散液に、エラストマーと溶剤とを含むエラストマー溶液を加えて液状組成物を調製する液状組成物調製工程と、
該液状組成物を基材に塗布し、塗膜を硬化させることにより、入射角20°で測定される表面の光沢度が0.4%より大きく10%より小さい導電性膜を得る硬化工程と、
を有することを特徴とする導電性膜の製造方法。 - 前記導電剤分散液は、分散剤を含む請求項7に記載の導電性膜の製造方法。
- 前記黒鉛粉末および前記膨張黒鉛粉末の平均粒子径は、45μm以上である請求項5ないし請求項8のいずれかに記載の導電性膜の製造方法。
- 前記粉砕処理工程において、前記粉砕処理を2回以上繰り返す請求項5ないし請求項9のいずれかに記載の導電性膜の製造方法。
- 前記導電剤のうち、前記黒鉛および前記膨張黒鉛の配合量は、該導電剤を除く固形分全体を100質量部とした場合の20質量部以上60質量部以下である請求項5ないし請求項10のいずれかに記載の導電性膜の製造方法。
Priority Applications (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201780003549.8A CN108885919B (zh) | 2016-03-30 | 2017-03-09 | 导电性膜及其制备方法 |
JP2017564148A JP6321894B2 (ja) | 2016-03-30 | 2017-03-09 | 導電性膜およびその製造方法 |
DE112017000178.1T DE112017000178T5 (de) | 2016-03-30 | 2017-03-09 | Leitender Film und Verfahren zu dessen Herstellung |
US15/952,705 US10978216B2 (en) | 2016-03-30 | 2018-04-13 | Conductive film and method for producing the same |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2016067488 | 2016-03-30 | ||
JP2016-067488 | 2016-03-30 |
Related Child Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US15/952,705 Continuation US10978216B2 (en) | 2016-03-30 | 2018-04-13 | Conductive film and method for producing the same |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2017169627A1 true WO2017169627A1 (ja) | 2017-10-05 |
Family
ID=59963126
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/JP2017/009470 WO2017169627A1 (ja) | 2016-03-30 | 2017-03-09 | 導電性膜およびその製造方法 |
Country Status (5)
Country | Link |
---|---|
US (1) | US10978216B2 (ja) |
JP (1) | JP6321894B2 (ja) |
CN (1) | CN108885919B (ja) |
DE (1) | DE112017000178T5 (ja) |
WO (1) | WO2017169627A1 (ja) |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020157999A1 (ja) | 2019-01-31 | 2020-08-06 | 住友理工株式会社 | 圧電センサおよびその製造方法 |
WO2021019923A1 (ja) * | 2019-07-30 | 2021-02-04 | 積水ポリマテック株式会社 | 導電性組成物、導電性膜、接点部材および導電性組成物の製造方法 |
WO2022138908A1 (ja) | 2020-12-25 | 2022-06-30 | 住友理工株式会社 | 導電性組成物、それを用いたシート状柔軟電極およびその製造方法 |
JP2022163756A (ja) * | 2021-04-15 | 2022-10-27 | 株式会社常光 | 薄片化黒鉛の製造方法 |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR20220040824A (ko) * | 2020-09-24 | 2022-03-31 | 삼성전자주식회사 | 연신 소자용 적층 구조체, 연신 소자 및 그 제조 방법, 표시 패널, 센서 및 전자 장치 |
CN113436787B (zh) * | 2021-06-30 | 2023-02-28 | 江苏科麦特科技发展有限公司 | 一种热敏性导电膜及其制备方法和用途 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011001910A1 (ja) * | 2009-06-30 | 2011-01-06 | 東海ゴム工業株式会社 | 柔軟導電材料およびトランスデューサ |
WO2011145411A1 (ja) * | 2010-05-19 | 2011-11-24 | 東海ゴム工業株式会社 | 導電膜、およびそれを用いたトランスデューサ、フレキシブル配線板 |
WO2013146262A1 (ja) * | 2012-03-29 | 2013-10-03 | 東海ゴム工業株式会社 | 導電性組成物および導電膜 |
WO2013146254A1 (ja) * | 2012-03-29 | 2013-10-03 | 東海ゴム工業株式会社 | 導電性組成物および導電膜 |
JP2015079725A (ja) * | 2013-09-13 | 2015-04-23 | 東洋紡株式会社 | 導電性ペースト |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US6037400A (en) * | 1997-08-25 | 2000-03-14 | Hitachi Maxell, Ltd | Composition for prevention of electric wave in wide range and electric wave absorber coping with all directions using same |
US7282260B2 (en) * | 1998-09-11 | 2007-10-16 | Unitech, Llc | Electrically conductive and electromagnetic radiation absorptive coating compositions and the like |
JP5278038B2 (ja) | 2008-02-26 | 2013-09-04 | 日本精工株式会社 | エラストマートランスデューサー |
US20100000441A1 (en) * | 2008-07-01 | 2010-01-07 | Jang Bor Z | Nano graphene platelet-based conductive inks |
JP5836368B2 (ja) * | 2010-06-18 | 2015-12-24 | ユニオン カーバイド ケミカルズ アンド プラスティックス テクノロジー エルエルシー | 導電性オレフィンマルチブロックコポリマー組成物 |
EP2562766A1 (de) | 2011-08-22 | 2013-02-27 | Bayer MaterialScience AG | Kohlenstoffnanoröhren und Graphenplättchen umfassende Dispersionen |
US20160059444A1 (en) | 2014-08-29 | 2016-03-03 | Yanbo Wang | Production of highly conductive graphitic films from polymer films |
-
2017
- 2017-03-09 CN CN201780003549.8A patent/CN108885919B/zh active Active
- 2017-03-09 WO PCT/JP2017/009470 patent/WO2017169627A1/ja active Application Filing
- 2017-03-09 DE DE112017000178.1T patent/DE112017000178T5/de active Pending
- 2017-03-09 JP JP2017564148A patent/JP6321894B2/ja active Active
-
2018
- 2018-04-13 US US15/952,705 patent/US10978216B2/en active Active
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2011001910A1 (ja) * | 2009-06-30 | 2011-01-06 | 東海ゴム工業株式会社 | 柔軟導電材料およびトランスデューサ |
WO2011145411A1 (ja) * | 2010-05-19 | 2011-11-24 | 東海ゴム工業株式会社 | 導電膜、およびそれを用いたトランスデューサ、フレキシブル配線板 |
WO2013146262A1 (ja) * | 2012-03-29 | 2013-10-03 | 東海ゴム工業株式会社 | 導電性組成物および導電膜 |
WO2013146254A1 (ja) * | 2012-03-29 | 2013-10-03 | 東海ゴム工業株式会社 | 導電性組成物および導電膜 |
JP2015079725A (ja) * | 2013-09-13 | 2015-04-23 | 東洋紡株式会社 | 導電性ペースト |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2020157999A1 (ja) | 2019-01-31 | 2020-08-06 | 住友理工株式会社 | 圧電センサおよびその製造方法 |
US11737710B2 (en) | 2019-01-31 | 2023-08-29 | Sumitomo Riko Company Limited | Piezoelectric sensor and method for manufacturing the same |
WO2021019923A1 (ja) * | 2019-07-30 | 2021-02-04 | 積水ポリマテック株式会社 | 導電性組成物、導電性膜、接点部材および導電性組成物の製造方法 |
JP6845602B1 (ja) * | 2019-07-30 | 2021-03-17 | 積水ポリマテック株式会社 | 導電性組成物、導電性膜、接点部材および導電性組成物の製造方法 |
WO2022138908A1 (ja) | 2020-12-25 | 2022-06-30 | 住友理工株式会社 | 導電性組成物、それを用いたシート状柔軟電極およびその製造方法 |
JP2022163756A (ja) * | 2021-04-15 | 2022-10-27 | 株式会社常光 | 薄片化黒鉛の製造方法 |
JP7466125B2 (ja) | 2021-04-15 | 2024-04-12 | 株式会社常光 | 薄片化黒鉛の製造方法 |
Also Published As
Publication number | Publication date |
---|---|
US10978216B2 (en) | 2021-04-13 |
US20180233250A1 (en) | 2018-08-16 |
DE112017000178T5 (de) | 2018-07-19 |
JP6321894B2 (ja) | 2018-05-09 |
JPWO2017169627A1 (ja) | 2018-04-05 |
CN108885919A (zh) | 2018-11-23 |
CN108885919B (zh) | 2020-03-31 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
JP6321894B2 (ja) | 導電性膜およびその製造方法 | |
JP6319085B2 (ja) | 導電性ペースト | |
Aakyiir et al. | Combining hydrophilic MXene nanosheets and hydrophobic carbon nanotubes for mechanically resilient and electrically conductive elastomer nanocomposites | |
JP5829328B2 (ja) | 導電性組成物および導電膜 | |
US20110133134A1 (en) | Crosslinkable and Crosslinked Compositions of Olefin Polymers and Graphene Sheets | |
TWI682405B (zh) | 導電性銀糊劑 | |
JP6155339B2 (ja) | 柔軟導電材料およびトランスデューサ | |
JP6690528B2 (ja) | 導電性膜 | |
Wang et al. | Polyaniline coated carbon nanotube/graphene “sandwich” hybrid and its high-k epoxy composites with low dielectric loss and percolation threshold | |
US20200140638A1 (en) | Method for producing electroconductive film | |
KR20130068436A (ko) | 탄소나노입자가 도입된 에폭시수지기반 전기 발열 복합필름 및 그 제조방법 | |
JP2015079724A (ja) | 導電性ペースト | |
Wu et al. | Latex co‐coagulation approach to fabrication of polyurethane/graphene nanocomposites with improved electrical conductivity, thermal conductivity, and barrier property | |
JP2014133842A (ja) | 導電性樹脂組成物 | |
JP6424054B2 (ja) | 柔軟導電材料およびその製造方法、並びに柔軟導電材料を用いたトランスデューサ、導電性テープ部材、フレキシブル配線板、電磁波シールド | |
KR101805949B1 (ko) | 폴리올레핀계 수지 조성물 및 그의 제조 방법 | |
JP2015079725A (ja) | 導電性ペースト | |
Wu et al. | Grafting rubber chains onto boron nitride nanosheets for highly flexible, thermally conductive composites | |
KR102051762B1 (ko) | 신축성 페이스트 조성물 | |
KR20030026352A (ko) | 폴리이미드 수지 조성물 및 그것으로 이루어지는폴리이미드 필름상 성형체 및 중간 전사 벨트 | |
JP2015065139A (ja) | 導電性ペースト | |
JP2016115561A (ja) | 導電性ペースト | |
JP2019143094A (ja) | 導電性塗料、および導電性皮膜 | |
KR20150076632A (ko) | 그래핀 복합체 및 그 제조방법 | |
KR20160116599A (ko) | 도전성 복합체 제조용 조성물, 이로부터 제조된 복합체, 및 이를 포함한 전자 소자 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
ENP | Entry into the national phase |
Ref document number: 2017564148 Country of ref document: JP Kind code of ref document: A |
|
WWE | Wipo information: entry into national phase |
Ref document number: 112017000178 Country of ref document: DE |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application |
Ref document number: 17774172 Country of ref document: EP Kind code of ref document: A1 |
|
122 | Ep: pct application non-entry in european phase |
Ref document number: 17774172 Country of ref document: EP Kind code of ref document: A1 |